Library

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • 1990-1994  (10,772)
  • 1920-1924
  • 1905-1909
  • 1993  (10,772)
  • Chemistry  (10,772)
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 204 (1993), S. 51-61 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Dielektrizitätskonstante (ε′) nd dielektrischer Verlust (ε″) von drei Carboxymethylcellulose-Proben mit verschiedenem Substitutions- und Polymerisationsgrad wurden im Frequenzbereich 0,1 - 10000kHz bei Temperaturen zwischen 10 und 60oC gemessen. Im Gegensatz zu nativer Baumwollecellulose, die zwei Relaxztionsprozesse (β und γ) zeigt, wurde nur jeweils ein Relaxationsprozeß zwischen 0,1 und 1kHz gefundern. Die dielektrischen Eigenschaften hängen dabei nicht nur vo Substritutionsgrad, sondern auch vom gewichtsmittleren Polymerisationsgrad und der Homogenität der Substitution ab.
    Notes: The dielectric constant, ε′, and dielectric loss, ε″, were determined for three solid carboxymethyl cellulose samples having different levels of substitution and different degrees of polymerization over a frequency range of 0.1 - 10 000 kHz at temperatures from 10-60°C. In contrast to the two relaxation processes, γ and β, previously observed in native cotton cellulose, only one relaxation process within a frequency range of 0.1 - 1 kHz was identified. It was found that the dielectric properties do not only depend on the degree of substitution, but also on the weight-average degree of polymerization and uniformity of distribution.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 204 (1993), S. 63-71 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Es wird ein neues Kapillar-Rheometer beschrieben, bei dem der Druck, mit dem die Meßflüssigkeit durch die Kapillaren gepreßt wird, durch eine hydraulische Vorrichtung erzeugt wird. Das Gerät ist voll zautomatisiert und wird durch einen PC gesteuert. Verschiedene Meß-Moden können vorgewählt und dann automatisch ausgeführt werden. Einige vorläufige Ergebnisse an Newtonschen Flüssigkeiten und an Polymerlösungen zeigen das Funktionieren des neuen Rheometers.
    Notes: A new capillary rheometer design is described, in which a hydraulic device is used to produce the pressure driving the sample fluid through capillaries. The device is fully automated and controlled by a PC unit. Various measuring modes can be preselected and are automatically executed. Some preliminary results with New tonian fluids and with polymer solutions show the functioning of the new rheometer.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 204 (1993), S. 73-83 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Naphthochinonderivate wurden als Elektronen- und Protonenüberträger in Polymermembranen für Redoxreaktionen eingesetzt. Eine solche, Vitamin K1 enthaltende Membran, läßt den Oxidations-Reduktions-Prozeß zwischen zwei wäßrigen Lösungen von Eisen(III) cyanid bzw. Natriumdithionit nur ziemlich langsam ablaufen. Ein effektiverer Überträger war Vitamin K3; die Reaktion verlief zunächst rasch, jedoch beiweideerholten Anwendungen immer langsamer, da ein Teil dieses, in senier reduzierten Form wasserlöslichen Überträgers während der Reaktion aus der Membran herausgelöst wurde. 2-Alkyloxy-1,4-naphthochinone wie z.B. das Hexyloxyderivat erwiesen sich als wirksame, die Reaktion unterstützende Elektronen- und Protonenüberträger, und in diesen Fällen führten wiederholte Anwendungen nicht zu Verzögerungen.
    Notes: A redox reaction was mediated by polymeric membranes which contain naphthoquinone derivatives as electron and proton carriers. When such a membrane containing vitamin K1 was placed between two aqueous solutions of potassium ferricyanide and sodium dithionite, the oxidation-reduction of them took place, but the reaction was rather slow. Although vitamin K3 was a more effective carrier and the reaction proceeded fast, the reaction rate decreased in the repeated runs. Since the reduced form of this carrier is slightly soluble in water, a part of the carrier got dissolved in the aqueous phase from the membrane during the reaction. 2-Alkyloxy-1,4-naphthoquinones such as 2-hexyloxy-1,4-naphthoquinone effectively transported electrons and protons through the polymeric membranes, promoting the membrane-mediated reaction; in these cases no retardation was observed in the repeated runs.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 4
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: The peroxide-initiated copolymerisation of an unsaturated polyester with zinc acrylate, diallyl phthalate prepolymer and a solid vinyl ester resin was investigated. The curing was followed by means of gelation curves and differential scanning calorimetry. The studies showed that zinc acrylate has the highest reactivity.
    Notes: Die Peroxid-initiierte Copolymerisation eines ungesättigten Polyesters mnit Zinkacrylat, Diallylphthalat-Prepolymer und einem Vinylesterharz wurde untersucht. Der Härtungsverlauf wurde anhand der Gelierungskurven und mitels Differentialkalorimetrie verfolgt. Die Prüfungen zeigten, daß Zinkacrylat die größte Reaktivität hat.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 204 (1993), S. 91-100 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Kinetik der isothermen Kristallisation des anionisch hergestellten Copolyamids PA 8/12 aus ω-Octanlactam (OL) und ω-Laurinlactam (12-Dodecanlactam) (LL) wurde nach der Avrami-Gleichung über den gesamten Zusammensetzungsbereich mittels DSC untersucht. Die Kristallisationsparameter Halbwertszeit (t1/2), Avrami-Index (n), Geschwindigkeitskonstante (k) und Kristallinitätsgrad wurden für verschiedene Kristallisationstemperaturen bestimmt. Eine Beziehung dieser Parameter zur Copolyamidzusammensetzung sowie zu Kristallisations- und Unterkühlungstemperaturen wurde untersucht und die Ergebnisse diskutiert. Desweiteren wurden die Werte de hier behandelten mit denen der in der Literaturgeschriebenen Homopolymeren verglichen.
    Notes: The isothermal crystallization kinetics of the anionic copolyamides of ω-octanelactam (OL) with ω-laurolactam (LL) (nylon-8/nylon-12), covering a wide composition range (0/100 - 100/0 OL/LL, mol/mol), was established according to the Avrami equation by the use of differential scanning calorimetry. The crystallization parameters half-time crystallization (t1/2), Avrami index (n), rate constant (k), and reduced crystallinity were determined for various crystallization temperatures. These parameter values are correlated to the composition of the copolyamides, the crystallization and supercooling temperature, and the results are discussed.Differences in kinetic parameter values between the homopolymers of this paper and those for the hydrolytic nylon-8 and nylon-12 reported in literature were observed and discussed.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 204 (1993), S. 111-118 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Abhängig von den Fällbedingungen tritt Poly(p-phenylen-1,3,4-oxadiazole) in zwei Modifikationen auf. Dies kann sowohl durch FTIR-Spektroskopie als auch mit Röntgenweitwinkelstreuung nachgewiesen werden. In beiden Fällen zeigt jede Modifikation charakteristische Peaks. Bei der Verarbeitung zu Fäden oder Filmen aus Lösungen in konzentrierter Schwefeläure durch Fällen in Wasser wird die im thermodynamischen Ungleichgweicht stehende β-Modifikation erhalten. Unter speziellen Bedingungen ist es möglich, die dreidimensional geordnete Gleichgewichtsstruktur direkt herzustellen. Verarbeitungsprodukte aus dieser α-Modifikation weisen merklich höhere Festigkeiten auf.
    Notes: Depending on the coagulation conditions, poly(p-phenylene-1,3,4-oxadiazole) in the solid state forms two modifications, as can be evidenced by FTIR spectroscopy and by wide-angle X-ray scattering curves (WAXS). In both cases each modification is detectable by characteristic peaks. Processing of fibers or films from solutions in concentrated sulfuric acid by coagulation in water results in the formation of a thermodynamically non-equilibrium form, defined as β-modification. Under special conditions it is possible to obtain the three-dimensionally ordered equilibrium α-structure that leads to processing products with markedly higher tenacities.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 204 (1993), S. 101-110 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: By a new technique for the addition of monomers it is possible to increase the reproducibility of the synthesis of poly(1,4-phenylene-1,3,4-oxadiazoles) by one order of magnitude in relation to the known method, measured by the standard deviation of the relative viscosity of polymer solutions in concentrated sulfuric acid. This method leads to polymers with very high molecular weights under markedly milder reaction conditions and in shorter reaction times than by the classic method.The influence of the most important reaction parameters on the reaction rate and equilibrium of the polycondensation was investigated. An [η]/Mw-relation was established based on light-scattering and viscometric investigations of polymer solutions in concentrated sulfuric acid.
    Notes: Die Reproduzierbarkeit der Synthese von Poly(p-phenylen-1,3,4-oxadiazolen) in Oleum Kann durch eine veränderte Monomerzugabetechnik, gemessen an der Standardabweichung der relativen Lösungsviskosität, um eine Größenordunung verbessert werden. Die Polykondensation verläft unter deutlich milderen Bedingungen in kürzeren Reaktionszeiten zu Polymeren mit höheren Molmassen als nach der bekannten Methode.Der Einfluß verschiedener Parameter auf die Reaktionsgeschwindigkeit und das Polykondensationsgleichgewicht wurde eingehend untersucht. Auf der Basis streulicht photometrischer und viskosimetrischer Messungen an Polymerlösungen in konzentrierter Schwefelsäure wurde eine [η]/Mw-Bezeihung ermittelt.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 204 (1993), S. 127-137 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Water-borne paints have received greater attention. Existing concepts related to suitable binders are polymethacrylate dispersions crosslinkable by autoxidation. Essential synthesis steps of such dispersions and characteristic properties also of adequate coatings are described.Oil fatty acid structure units are enriched in the shell-region of the dispersed particles and the rest of nearly 30% is localized in the water phase as substituent of a water-soluble copolymer.
    Notes: Wäßrige Anstrichsysteme setzen sich in zunehmendem Maße durch. Als eine Entwicklungsvariante für diesbezüglich geeignete Bindemittel kommen autoxidativ vernet zende Polymethacfrylatdispersionen in Betracht. Es werden wesentliche Schritte der Synthese derartiger Dispersionen un dcharakteristische Eigenschaften auchvon Beschichtungen vorgestellt.Die Ölfettsäurestruktureinheiten sind im Schalenbereich der disperigierten Teilchen angereichert, und sie befinden sich außerden zu etwa 30% in der wäßrigen Phase als Substituenten eines löslichen Copolymeren.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 204 (1993), S. 153-159 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Ein hochvernetztes duroplastisches Epoxidharz wurde durch “reactive blending” in Gegenwart von Bisphenol A-Polycarbonat (PC) modifiziert. FTIR-Untersuchungen zeigten, daß der Umsatz nach dem Härtungs- und Nachhärtungsprozeß durch den PC-Anteil im Blend erniedrigt wird. Darüber hinaus wurde beobachtet, daß Bruch festigkeit des Blendsystems mit wachsendem PC-Gehalt merklich steigt. Für die Phasentrennung der Unterschußkomponente während der Vernetzung wurden keine Beweise gefunden.
    Notes: A highly crosslinked thermosetting epoxy resin was modified by a reactive blending process carried out in the presence of bisphenol-A polycarbonate (PC). FTIR spectroscopy investigations demonstrated that the presence of PC in the blend decreases the reactants conversion after the curing and postcuring processes. Moreover, it was found that the fracture toughness of this blend system increases markedly by increasing the PC content in the blend. No evidence of phase separation of the minor component during the crosslinking reaction steps was observed.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 204 (1993), S. 119-125 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die antibakterielle Wirkung von Homopolymeren von Cetyldimethyl(4-vinylbenzyl)ammoniumchlorid (VB16), Lauryldimethyl(4-vinylbenzyl) ammoniumchlorid (VB12) und TRimethyl(4-vinylbenzyl)ammoniumchlorid (VB1) und deren Copolymeren mit Acrylnitril wurde untersucht. Alle Homo- und Copolymeren wirkten bei den getesteten Bakterienarten-B. subtilis, S. aureus, E. coli und P. aeruginosa - keimtötend. Besondrs stake Effekte zeigten sich bei gram-positiven B.-subtilis- und S.-aureus-Kulturen. Die keimtötende Wirkung nahim in der Reihe VB16 〉 VB12 ≫ VB1 ab.
    Notes: Homopolymers of cetyldimethyl(4-vinylbenzyl)ammonium chloride (VB16), lauryl-dimethyl(4-vinylbenzyl)ammonium chloride (VB12), and trimethyl (4-vinylbenzyl)ammonium chloride (VB1), and copolymers of these compounds with acrylonitrile were examined for antibacterial activity using B. subtilis, S. aureus, E. coli, and P. aeruginosa. All homopolymers and copolymers showed germicidal action to the bacterias, especially strong action to gram-positive B. subtilis and S. aureus. The strength of the germicidal action of the quaternary ammonium branches was in the order: VB16 〉 VB12 ≫ VB1.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 11
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 204 (1993), S. 161-175 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: The permeability of gases in films and membranes of thermoplastic starch (TPS) was investigated. The permeability- and diffusion coefficients were measured with the time-lag method on films on TPS with different plasticizer contents and at different temperatures. The experimentally determined low permeabilities were comparable to those of synthetic polymers available on the market. TPS shows at low water activities permeabilities similar to good gasbarrier materials. With increasing water content - as it is already shown for other hydrophilic polymers - the gasbarrier property of TPS gets lost. Together with earlier works on the structure and the thermodynamical behaviour of the starch, the molecular parameters and their influence on the permeability were discussed.
    Notes: Als Alternative zu den heutigen Massenkunststoffen wurde die Möglichkeit eines Einsatzes von thermoplastischer Stärke (TPS) als Barrierewerkstoff in Filmen und Membranen untersucht. Die Permeations- und Diffusionskoeffizienten wurden mitels der Induktionszeit-Methode an Filmen aus TPS in Abhängigkeit von Temperatur und Weichmachergehalt ermitelt. Die expermentell gefundence gute Gasbarriereeigen schaft der Stärke gegenüber Sauerstoff und Stickstoff wurde durch vergleichende Messungen an Handelsprodukten ergänzt. Die TPS zeigt bei nieedrigen Wassergehalten denhandelsüblichen Barrierepolymeren vergleichbare Gaspermeationsraten. Mit steigen dem Wassergehalt verliert sie- wie die meisten hydrophilen Polymere - ihre Gasbarrierewirkung.Gemeinsam mit früheren Arbeiten über die Struktur und die Eigenschaften von thermoplastischer Stärke wurden die molekularen Parameter und ihr Einfluß auf die Gasdurchlässigkeit diskutiert.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 12
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Durch Phasengrenzflächenpolykondensation von 4,4'-Bis(mercaptomethyl)biphenyl mit ausgewählten aliphatischen und isomeren Phthalsäuredichloriden wurden neue Polythioester erhalten.Um die optimalen Bedingungen der Phasengrenzflächenploykondensation zu bestimmen, wurde der Einfluß folgender Faktoren auf die reduzierte Viskosität and die Ausbeute der Polythioester ermittelt: Art der organischen Phase, Konzentration der Reagenzien. Verhältnis der wässeigen zur organischen Phase, Art und Konzentration des HCI-Akzeptors, Reaktionstemperatur und -zeit. Die Polykondensation von Dithiol mit Adipinisäuredichlorid und Isophthalsäuredichlorid wurde als Modellsystem genauer untersucht. Die Polythioesterstrukturen wurden mittels Elementaranalyse, IR-Spektroskopie und Röntgenstrukturanalyse bestätigt. Aus der thermogravimetrischen Analyse wurde die Zersetzungstemperatur, der Gewichtsverlust bei dieser Temperatur und das Maximum der Zersetzungsgeschwindigkeit erhalten. Es wurden weiterhin einige physikalisch-chemische, mechanische und dielektrische Eigenschaften ermittelt. Aufgrund der schlechten Löslichkeit der Polythioester konnten die mittleren Molekulargewichte nicht bestimmt werden.
    Notes: New polythioesters were synthesized by interfacial polycondensation of 4,4'-bis(mercaptomethyl)biphenyl with selected aliphatic and isomeric phthaloyl dichlorides.To determine optimum polycondensation conditions, the influence of the following factors on reduced viscosity and yield were studied: type of organic phase, concentration of reagents, aqueous/organic phase ratio, type and concentration of hydrogen chloride acceptor, rate of acid chloride addition, reaction temperature and reaction time.A thorough examination was carried out only for the polycondensation of dithiol with adipoyl and isophthaloyl dichlorides chosen as a model system. The structures of polythioesters were confirmed by elemental analysis, X-ray analysis and infrared spectroscopy. The temperature of initial decomposition, the percentage of its mass loss, and temperature of the fastest decomposition process from curves of differential and thermogravimetric analysis were determined. Some physicochemical, mechanical and electrical properties were determined. The molecular weights were not measured because of the low solubility of the obtained polythioesters.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 13
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 204 (1993), S. 177-189 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Investigations on chemical coupling of heterogeneous polystyrene-polybutadiene blends were carried out using an organic sulfonylazide. The coupling process was realized in the melt mixing process on a laboratory melt kneader. The efficiency of the coupling agent was evaluated by IR-spectroscopical, microscopical, and dynamic-mechanical analysis and by mechanical properties of the blends. The graft copolymers forming in the melt cause an increase of the stress-strain properties and the impact strength of the blends.
    Notes: Es wurden Untersuchungen zur chemischen Kopplung heterogener Polystyrol-Polybutadien-Blends bei Einsatz eines organischen Sulfonylazids während des Schmelzemischens im Laborinnenmischer angestellt. Die Wirksamkeit des Kopplungsagens wurde anhand infrarotspektroskopischer, mikroskopischer und dynamisch-mechanischer Analysen sowie anhand des merchanischen Eigenschaftsbildes der Belends beurteilt. Die sich in der Schmelze bildenden Pfropfcopolymeren führen zu einer Erhöhung der Phasenwechselwirkungen un dami zu einer Verbesserung der Festigkeits- und Zähigkeits-eigenschaften der Blends.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 14
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 205 (1993), S. 19-30 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Interpenetrating polymer networks (IPN) were obtained by the simultaneous crosslinking of unsaturated polyester resins and Bisphenol A dicyanate. The copolymerization of the unsaturated polyester with styrene occurred according to the radical mechanism, whereas Bisphenol A dicyanate underwent a cyclotrimerization, thus forming a polytriazine (polycyanurate) network. The IPNs are characterized by elevated glass transition temperature and increased mechanical strength in comparison with corresponding unsaturated polyester resin without Bisphenol A dicyanate.
    Notes: Interpenetrierende Polymernetzwerke (IPN) wurden durch die gleichzeitige Vernetzung ungesättigter Polyesterharze und Dian-Dicyanat erhalten. Die Copolymerisation von ungesättigtem Polyester mit Styrol erfolgte nach dem radikalischen Mechanismus, während das Dian-Dicyanat cyclotrimerisierte, wodurch sich ein Polytriazin(Polycyanurant)- Netzwerk bildete. Die IPN zeichnen sich durch erhöhte Glastemperatur und mechanische Festigkeit im Vergleich zum entsprechenden ungesättigten Polyesterharz ohne Dian-Dicyanat-Zusatz aus.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 15
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 205 (1993), S. 1-17 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Simultaneous TG/DTA analysis has been used for determination of surface coating of CaCO3-filler with stearic acid (STS) or isopropyl triisostearoyl titanate (titanate). The method has been used for several model samples as well as for commercial fillers with surface coating concentrations of 0-2.7% for stearic acid and 0-4.0% for titanate. A reliable agreement of surface coating concentration of STS determined by simultaneous TG/DTA analysis and C-analysis was achieved if the temperature range of decomposition of the surface-modifying agent was taken into account. This was found for stearic acid between 180 and 450°C (〉1% STS at 500°C) and for titanate between 120 and 450°C (〉 1% titanate at 500°C) from the slopes of the TG- and DTA curves. The mass loss in the range of decomposition is equal to the concentration of surface coating in the case of STS. For titanate-modified fillers an amount of 10% of the mass loss must be added. For determination of surface coating of CaCO3-fillers having higher contents of humidity (〉 0.2%) it is necessary to know this amount, otherwise the STS determination has to be performed by oxidation heat.
    Notes: Zur Bestimmung des Modifikatorgehaltes von Stearinsäure(STS)-bzw. Isopropyltriisostearyltitanat(Titanat)-modifizierten CaCO3-Füllstoffen wurde die simultane TG/DTA-Analyse genutzt. die Methode wurde für Modellproben sowie für verschiedene kommerzielle Füllstoffe mit einem Konzentrationsbereich von 0 - 2,7% STS bzw. 0 - 4% Titanat angewendet. Eine ausreichende Übereinstimmung der Modifikatorkonzentrationen für STS, bestimmt durch simultane TG/DTA-Analyse sowie eine C-Analyse, wird erreicht, wenn der Zersetzungsbereich des Modifikators berücksichtigt wird. Dieser liegt für Stearinsäurezwischen180°C und 450°C (bei STS 〉 1% bei 500°C) und für Isopropyltriisostearyltitanat zwischen 120 und 450°C (Titanat 〉 1% bei 500°C) und wird aus dem Anstieg der TG-bzw. DTA-Kurve erhalten. Der diesem Zersetzungsbereich zuzuordnende Masseverlust entspricht bei STS-modifizierten Füllstoffen dem Stearinsäuregehalt. Bei Titanat-modifizierten CaCo3-Füllstoffen ist ein Betrag von 10% des Masseverlustes hinzuzufügen. Für die Modifikatorgehaltsbestimmung von CaCo3-Füllstoffen, die einen höheren Feuchtigkeitsgehalt (〈 0,2%) aufweisen, ist die Kenntnis dieser Größe notwendig, anderenfalls ist die STS-Bestimmung über die Oxidationswärme zu realisieren.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 16
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 204 (1993), S. 191-191 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 17
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 205 (1993), S. 31-45 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Entfernung von Methylorgane (MO) aus Wasser oder einer Pufferlösung (pH7) durch Adsorption and Reaktionsprodukten von Poly(gylcidylmethacrylat) (PGMA) mit Tetraethylenpentamin oder mit einem Polyethylenimin mit einem Molekulargewicht von 600 (PE1600) wurde untersucht. Das Adsorptionsverhalten läßt sich besser mit der Freundlich-Gleichung als mit der Klotz-Gleichung beschreiben. Adsorptionsgeschwindigkeit und adsorbierte Menge waren in Wasser größer als in der Pufferlösung, in der durch Salzbildung die Adsorption vermindert wird. Die adsorbierte Menge hängt nicht immer von der Menge der an PGMA gebundenen PE1600-Gruppen ab.
    Notes: A study was made of the removal of methyl orange (MO) solutes in water and in a pH 7 buffer solution by the reaction products of insoluble poly(glycidyl methacrylate) (PGMA) with tetraethylenepentamine (TEP) or polyethylenimine (PEI) having molecular weight of about 600 (PEI600). An examination was made of the adaptability of the Freundlich adsorption formula and the Klotz equation to removal behaviour of these polymers, which was noted to conform better to the Klotz equation than to the Freundlich adsorption formula. The removal rate and the amount removed were greater in water than in a pH 7 buffer solution, and decreased due to coexisting salts. The amount removed does not always depend on the amount of PEI600 groups bound to PGMA.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 18
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 205 (1993), S. 59-74 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Das Zug-Dehnungs-Verhalten von verschiedenen Blends aus Poly(ethylen-co-vinylacetat) (EVA, 28 wt.-% VA-Anteil) und Polyethylen (LDPE) wurde bei unterschiedlichen Dehnungsgeschwindigkeiten und Temperaturen untersucht. Die Zug-Dehungs-Kurven solcher semikristalliner Polymerblends bestehen aus drei Teilen - elastischer oder Hookescher Bereich, Bereich des Aneinanderabgleitens der Ketten sowie Dehnungshärtungsbereich. Eine Verminderung der Dehnungsgeschwindigkeit bewirkt eine Vergrößerung des Dehnungshärtungsbereiches. Die Erhöhung der Meßtemperatur beeinflußt der Dehnungshärtung bei erhöhten Temperaturen vom Kristallschmelzpunkt der Hauptkomponente des Blends abhängt. Röntgen- und DSC-Untersuchun-gen zeigen, daß die Dehnungshärtung von einer Veränderung der Kristallistruktur in LDPE und LDPE-reichen Blends ausgeht, während sie in EVA und EVA-reichen Blends auf eine induzierte Kristallisation in der amorphen Phase zurückzuführen ist.
    Notes: Stress-strain behaviour of different blends of poly(ethylene-co-vinyl acetate) (EVA) (28 wt.-% VA content) and low density polyethylene (LDPE) is studied under various strain rates and temperatures. It is found that stress-strain plots of such semicrystalline polymer blends consist of three parts, namely, elastic or Hookeian region, region of chain slippage and region of strain hardening. Decrease in strain rate has an increasing effect on the strain hardening region. Increase in measurement temperature adversely affects the whole stress-strain plot. It is apparent from the study that at an elevated temperature the process of strain hardening is dependent on the crystalline melting point of the major component in the blend. The X-ray and DSC studies reveal that the process of strain hardening is mainly due to a change in internal order of crystallites in LDPE and LDPE-rich blends, whereas in EVA and EVA-rich blends it is due to induced crystallization in the amorphous phase.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 19
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 205 (1993), S. 47-58 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Methylmethacrylat (MMA) mit einem Prepolymergehalt von 6-8% wurde mit unterschiedlichen Anteilen (1-20%) 2-Ethylhexylmethacrylat (EMMA), n-Hexylmethacrylat (HMA), 2-Ethylhexylacrylat (EHA) oder n-Hexylacrylat (HA) copolymerisiert. Aus den erhaltenen Copolymeren wurden Folien hergestellt, an denen der Einfluß der Copolymerstruktur auf Lichtdurchlässigkeit, Dichte und mechanische Eigenschaften ermittelt wurde. zugsfestigkeit and Speichermodul nahmen mit zunehmendem Comonomergehalt ab. Die Dehnung stieg im Fall von MMA/EHA- und MMA/HA-Copolymerfolien mit 15 und 20 Gew.-% Comonomeranteil merklich an. Mittels DMTA wurde die Erweichungstemperatur der Copolymeren bestimmt. Die HDT und die Erweichungstemperatur nahmen unter Biegebelastung mit steigendem Comonomergehalt de Copolymeren ab.
    Notes: The paper describes the fabrication of cast acrylic sheets by copolymerizing a prepolymer syrup of methyl methacrylate (MMA) with varying amounts (1-20 wt.-%) of 2-ethylhexyl methacrylate (EHMA), n-hexyl methacrylate (HMA), 2-ethylhexyl acrylate (EHA) and n-hexyl acrylate (HA). The effect of structure of copolymer on light transmittance, density and mechanical properties was evaluated. Tensile strength and storage modulus decreased with increasing comonomer content. Strain increased significantly in the case of MMA/EHA and MMA/HA copolymer sheets having 15 and 20 wt.-% of comonomer. Softening temperature of copolymer samples was determined using dynamic mechanical thermal analysis. Heat deflection temperature under flexural load and softening temperature decreased with increasing comonomer content in copolymer.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 20
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Poly[(N-(4-hydroxyphenyl)maleimid)-alt-(p-trimethylsilyl-a-methylstryol)] (a-PHTMMS) und einige N-(4-hydroxyphenyl)maleimid-alt-p-trimethylisilyl-a-methylstyrol-enthaltende Copolymere wurden synthetisiert, um mit Diazonaphtochinonsulfonat neue Resists für den nahen UV-Bereich (DNS) zu entwickeln.Durch die kettenversteifende Wirkung der Maleimid-Gruppe wurde eine hohe thermische Stabilität mit einer Glasübergangstemperatur von 240°C und einer Zersetzungstemperatur von 425°C erreicht. Daraus hergestellte lithographische Biler widerstanden noch bei 250°C thermischer Verformung. Die hergestellten siliciumhaltigen Resists wurden auch als oberste Schicht in zweischichtigen Materialien für die Anwendung in der Mikrolithographie untersucht.
    Notes: Poly[(N-(4-hydroxyphenyl)maleimide)-alt-(p-trimethylsilyl-α-methylstyrene)] (α-PHTMMS) and several N-(4-hydroxyphenyl)maleimide -alt-p-α-methylstyrene related copolymers were synthesized for novel positive near-UV resists containing diazonaphthoquinone sulfonate (DNS). The chain-stiffening effect of the maleimide group was responsible for high thermal resistance. Thus, a high glass transition temperature of 240°C and thermal decomposition temperature of 425°C were obtained. Lithographic positive images were obtained which resisted thermal deformation at 250°C. The prepared silicon-containing resists were also used as the top imaging layer of a bilayer resist for microlithographic application.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 21
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 205 (1993), S. 91-95 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Polymerisation von Styrol in Anwesenheit von Fluoreszenzfarbstoffen, Derivaten des Benzanthrons, wurde untersucht. Die Abhängigkeit der Polymerisationsgeschwindigkeit des Styrols vom Charakter des Farbstoffs wurde ermittelt. Spektrophotometrisch wurde festgestellt, daß 70-80% des Farbstoffs in das Polymere eingebaut werden, ohne daß dies zu einer bedeutenden Veränderung des Molekulargewichts und der Molekulargewichtsverteilung führt.
    Notes: The polymerization of styrene in the presence of some fluorescent dyes, benzanthrone derivatives, has been investigated. The dependence of the polymerization rate of styrene on the character of the dye was determined. It was found spectrophotometrically that 70 - 80% of the dye reacted in the polymerization, thus the coloured fluorescent polymers were obtained. They are resistant to wet treatment and decolouration by solvent. The incorporation of the dye into the polymer chain does not significantly affect the molecular weight and polydispersity of the coloured polymers.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 22
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Im vorliegenden Beitrag wird über die Veränderungen der dynamischen Moduli und der thermiscen Übergänge von Polyvinylidenfluorid in kompatiblen Blends mit Polymethylmethacrylat und in nicht kompatiblen Blends mit Polystyrol berichtet. Die Wirkung des Sepioliths auf die Kompatibilität dieser Blends wurde untersucht.
    Notes: This paper reports on a study of dynamic moduli and thermal transitions of poly(vinylidene fluoride) in compatible blends with poly(methylmethacrylate) and in non-compatible blends with polystyrene. The effects of sepiolite on the compatibility of these blends have been studied.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 23
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 205 (1993), S. 107-115 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Strahlungsvulkanisation von Naturgummilatex (NRL) mit n-Butylacrylat führt bei daraus hergestellten Filmen zu höheren Zugfestigkeiten. Die Alterungseigenschaften von strahlungsvulkanisiertem Naturgummi (RVNRL) wurden in Gegenwart unterschiedlicher Antioxidantien untersucht. Um für die Filme aus RVNRL geeignete Antioxidantien zu finden, wurde die Gelfraktion mit Xylol in Gegenwart von 1-Gew.-% Antioxidans unter einem Luftstrom extrahiert. Antioxidantien, die während der Extraktion einer durch oxidativen Abbau bedingten Verringerung des Gelanteils entgegenwirken, sind für die Alterungssuntersuchungen mit RVNRL geeignet. Es zeigte sich, daß Tris(nonylphenyl)phosphit (Nonflex TNP) und 2,5-Di-tert-amylhydrochinon (Antage DAH) unter 12 getesteten Antioxidantien am effektivsten waren.
    Notes: Radiation-vulcanization of natural rubber latex (NRL) with n-butyl acrylate gives a higher tensile strength for films obtained after casting. The ageing properties of radiation-vulcanized natural rubber in the presence of various antioxidants have been investigated. In order to find out suitable antioxidants for radiation-vulcanized natural rubber latex (RVNRL) films, extraction of the gel fraction was carried out in xylene with 1 wt.-% antioxidant and air bubbling. Antioxidants which give less reduction in gel fraction due to oxidative degradation during extraction are effective for ageing tests of RVNRL films. It was found that tris(nonylated phenyl) phosphite (Nonflex TNP) and 2,5-di-tert-amylhydroquinone (Antage DAH), among 12 different antioxidants tested, were the most effective antioxidants for RVNRL films.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 24
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 205 (1993), S. 131-139 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Stearinsäure bzw. Dibutylphthalat wurden als Adhäsionsverbesserer zu mit Calciumcarbonat gefüllten ternären Blends, bestehend aus einem Polyethylen/Poly(strol-co-divinylbenzol)-Interpolymeren und Polypropylen, zugegeben. Daraus wurden nach einem bereits beschriebenen Verfahren poröse Ionenaustauschermembranen (PIEM) hergestelt. Die Adhäsionsverbesserer führen dabei zu einer beträchtlichen Erhöhung des Porendurchmessers, da die Diffusion von Chlorsulfonsäure zu den Calciumcarbonatkörnern und damit die Bildung großer Mengen Kohlendioxid erleichtert wird. Andere PIEM-Eigenschaften werden nicht sigifikant beeinflußt.
    Notes: The previously described preparation of porous ion-exchange membranes (PIEM's) from the ternary blends of polyethylene interpolymer with poly(styrene-co-divinylbenzene) and polypropylene and calcium carbonate filler has been supplemented with the use of stearic acid and dibutyl phthalate as adhesion promoters. It was noted that both promoters govern the huge increase of pore diameter without any significant disturbances in the other PIEM's properties. The facilitating effect of chlorosulfonic acid diffusion toward calcium carbonate grains and large amounts of carbon dioxide volatilization was concluded. This is the basic point of pore creation to be discussed in this paper.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 25
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Makroporöse Membranen aus Terpolymeren von 2,3-Epoxypropylmethacrylat, N-Vinyl-2-pyrrolidon und Ethylendimethacrylat, wurden durch radikalische Suspensionscopolymerisation hergestellt und danach mit Ammoniak modifiziert. Charakteristische Eigenschaften der Membranen wei Porosität, spezifische Oberfläche, Porengröße, Wasserdurchlässigkeit und mechanische Eigenschaften wurden bestimmt. Ein niedriger Gehalt an N-Vinyl-2-pyrrolidon verbessert die mechanischen Eigenschaften der Membranen. Der Mechanismus der Bildung der makroporösen Struktur und der Heterogenitäten wird diskutiert.
    Notes: Macroporous membranes based on terpolymers of 2,3-epoxypropylmethacrylate, N-vinyl-2-pyrrolidone, and ethylenedimethacrylate were prepared by radical suspension copolymerization and subsequently modified with ammonia. The membranes were characterized by their porosity, specific surface area, pore size, water permeability and mechanical properties. The low content of N-vinyl-2-pyrrolidone improves the mechanical properties of the membranes. The mechanism of formation of the macroporous structure and heterogeneities is discussed.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 26
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: The aim of the studies was to characterize the ultrafiltration properties of a variety of photochemically modified membranes, made by a new approach starting with two types of PAN-UF membranes and using nine aromatic azides bearing different more or less hydrophilic or hydrophobic substituents. The influence of the surface functionalization (hydrophilization, introduction of charges/hydrophobization) realized by this means onto the water permeability, the dextrane selectivity, and the permeabilities during and after UF, resp., after simple contact with solutions of ovalbumine and lysozyme was the major subject. Modified membranes made using the aryl azides with hydrophilic groups, 4-azidobenzoic acid, Ib, (4-azidophenyl)trimethylammonium iodide, If, sodium (4-azido)-benzene sulfonate, Id, showed enhanced water fluxes and reduced dextrane retention. All the other azides caused reduced water permeability, enhanced dextrane selectivity, and significant flux reductions as a consequence of contact with ovalbumin solutions (pH = 5.0). The strongest effects were achieved with the two expecially hydrophobic compounds, 2-naphthyl azide, Ih, and 2-naphthoyl azide, IX. On the other hand, a pronounced positive effect of photo-modification on the protein fouling behaviour became evident in the UF of lysozyme (0.05%, pH = 10.5). Using the membranes modified with Id a much higher filtrate flux (Jv = 48.1 l/m2h) was observed as compared with the original PAN membrane (Jv = 13.1 I/m2h). The perspectives and the limitations of the developed modification strategy are discussed.
    Notes: Nach einem neuartigen Verfahren mit Hilfe von neun, mit verschieden hydrophilen bzw. hydrophoben Substituenten synthetisierten aromatischen Aziden unterschiedlich photochemisch modifizierten Polyacrylnitril-Ultrafiltrations-Membranen wurden in UF-Versuchen charakterisiert. Dabei sollte der Einfluß der so erzielten Oberflächenfunktionalisierungen (Hydrophilierung, Einführung von Ladungen oder Hydrophobierung) auf das Trennverhalten (Wasserdurchläassigkeit und Selektivitäat für Dextrane, Permeabilität während und nach der UF bzw. nach einfachem Kontakt mit Ovalbuminund mit Lysozym-Lösungen) studiert werden. Die Modifizierung mit den Arylaziden, die hydrophile Gruppen enthalten (4-Azidobenzoäure, Ib, (4-Azidophenyl)-tri-methylammoniumiodid, If, Natrium-4-azidobenzolsuflfonat, Id), führt zu einer erhöhten Durchlässigkeit der Membranen für Wasser und Dextrane. Alle anderen Azide, darunter besonders stark die deutlich hydrophoben 2-Naphthoylazid, Ih, und 2-Naphthoylazid, IX, verringern die Wasserpermeabilität, erhöhen das Rückhaltevermögen für Dextrane und verstärken die Effekte der Wechselwirkungen mit Ovalbumin (pH = 5,0). Das wird in Flußreduzierungen verglichen mit der unmodifizierten PAN-UF-Membran sichtbar. Ein positiver Effekt der Photomodifizierung wird besonders deutlich bei der UF von Lyasozym (0,05%, pH = 10,5) mit der mit Id modifizierten Membran (Jv = 48,1 l/m2h) im Vergleich zur Ausgangs-Membran (Jv = 13,1 1/m2h). Die Perspektiven und die Grenzen des Modifizierungsverfahrens werden abschließend diskutiert.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 27
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 210 (1993), S. 197-205 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: For solving specific problems of separation, high demands on membrane materials will be made in relation to thermal stability and resistance in a wide pH-range and against organic solvents. Membranes from poly(p-phenylen-1,3,4-oxadiazole) are prepared by different methods and their separation properties in ultrafiltration are investigated.
    Notes: Poly(p-phenylen-1,3,4-oxadiazol) (POD) ist aufgrund seiner thermischen Stabilität, pH- und Lösungsmittelbeständigkeit ein interessanter Werkstoff zur Herstellung von Membranen. Die Herstellung von POD-Membranen und deren Trenneigenschaften im Prozeß der Ultrafiltration werden untersucht.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 28
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 211 (1993), S. 79-87 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Ein Poly(sulfidsulfon) wurde durch aktivierte nucleophile Substitution der Nitrogruppen von Bis(4-nitrophenyl)sulfon mit wasserfreiem Natriumsulfid bei 200 C in N-Methyl-2-pyrrolidon (NMP) hergestellt. Das Polymere löst sich in NMP, Dimethylformamid (DMF), Dimethylsulfoxid und anderen hochpolaren Lösungsmitteln. Das Molekulargewicht des Polymeren mit einer inhärenten Viskosität von 15 ml/g bei 30°C in DMF wurde mittels 1H-NMR-Spektroskopie zu Mn = 2500 bestimmt. Die Glastemperatur liegt bei ca. 73°C; der Veraschungsrückstand bei 600°C in Luft beträgt 36%, der Sauerstoffindex (LOI) ca. 37.
    Notes: A poly(sulfide sulfone) was synthesized by activated nucleophilic displacement reaction between bis(4-nitrophenyl)sulfone and anhydrous sodium sulfide at 200°C in N-methyl-2-pyrrolidone (NMP). The polymer is soluble in NMP, dimethylformamide, dimethylsulfoxide and other highly polar solvents. The molecular weight of the polymer (M̄n = 2.500) having an inherent viscosity of 15 mL/g at 30°C in DMF was determined by 1H-NMR spectroscopy. The polymer has a glass transition at approx. 73°C and char residue of 36% at 600°C in air. The limiting oxygen index of the polymer is ∼37.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 29
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 211 (1993), S. 35-51 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Es wurden Untersuchungen durchgeführt, um ein auf experimentellen Ergebnissen basierendes mathematisches Modell zu entwickeln, welches die Durchmischung und andere Polymerisationsparameter mit der Partikelgröße von PVC korreliert und die Grenzen der Rührgeschwindigkeit in einem definierten Rührersystem festlegt.Dazu wurde eine Computer-Regressionsanalyse von etwa 30 in Reaktoren von 10L bis 27 m3 Volomen durchgeführten Vinylchlorid-Polymerisationen berechnet. Die Partikelgröße (d50) hängt dabei ab von den Polymerisationsparametern Rührerdurchmesser (D), Rührergeschwindigkeit (N), Durchmesser des Reaktorbehälters (T), Flüssigkeitsstand (H1) und Volumen des Reaktorbehälters (V) (NWe = Weber-Zahl): d50 = 4346.8 (N)-0.905 (D)-0.901 (T)-0.514 (H1)-0.131d50/D = 273292.1 NWe-0.51 undNmin = 3049.1 D-1.1 (T/D)-0.113In diesen Gleichungen sind nur die Werte 3049, 1, -0,113, 4346, 8 und 273 292, 1 abhängig von der Zusammensetzung des Polymerisationsgemisches. Wird dieses geändert, müssen diese Variablen anhand von einer oder zweier Polymerisationen im Pilotmaßstab ermittelt werden, um die Beziehungen an die neue Zusammensetzung anzupassen und so eine Übertragung auf einen größeren Reaktor zu ermöglichen.
    Notes: Studies were carried out to develop a mathematical model based on experimental results to correlate agitation and other polymerization parameters with the particle size of PVC and to specify the limits of agitation speed within the defined agitation system. Computer regression analysis of about 30 vinyl chloride polymerizations in reactors with 10 L to 27 m3 tank volume are carried out. The particle size of PVC (d50) is correlated to various polymerization parameters such as impeller diameter (D), impeller speed (N), reactor tank diameter (T), liquid height (H1) and tank volume (V) (NWe = Weber number): d50 = 4346.8 (N)-0.905 (D)-0.901 (T)-0.514 (H1)-0.131d50/D = 273292.1 NWe-0.51Nmin = 3049.1 D-1.1 (T/D)-0.113In these equations only the values 3049.1, -0.113, 4346.8 and 273 292.1 depend on the recipe. When the recipe is changed these variables must be determined by one or two bench-scale polymerizations to adjust the correlations to the new recipe conditions so that they can be also used for scale-up purposes with the new recipe.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 30
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 211 (1993), S. 61-77 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: 4-Phenyl-4-(2,3-expoxypropyl)benzoate (I) can be cured to thermoset networks with a different degree of order by using isomeric aminophenyl aminobenzoates II to V as curing agents. The formation of intermediates during the curing reaction was studied by means of model compounds. From the reaction of the monoamino-substituted phenylbenzoates VI to IX the reactivities for the primary and the secondary aminoprotons towards epoxide was determined. The kinetic data were used for a stepwise simulation of the curing reaction. Arguments were found that in case of diamines with 4-aminobenzoate structure well ordered intermediates are formed, which crosslink in an early stage of the reaction.
    Notes: Die Härtung von 4-Phenyl-4-(2,3-epoxypropoxy)benzoat (I) mit den isomeren Aminophenylaminobenzoaten II bis V führt zu unterschiedlich geordneten Epoxidnetzwerken. Die Bildung verschiedener Intemediate während der Härtungsreaktion wurde anhand von Modellverbindungen studiert. Aus der Reaktion der monoamino-substituierten Phenylbenzoate VI bis IX mit Epoxid wurden die Reaktionskostanten für die Addition an das primäre und das sekundäre Wasserstoffatom der Aminogruppen bestimmt. Die kinetischen Daten lassen sich für eine schrittweise Simulation des Härtungsverlaufs verwenden. Es wurden Argumente dafür gefunden, daß sich bei Verwendung der Amine mit 4-Aminobenzoat-Strukturen gut geordnete, schnell vernetzende Intermediate bilden.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 31
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 211 (1993), S. 89-101 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die diskontinuierliche Polymerisation von Butadien in Hexan bei 45°C mit einem in-situ-aktivierten Ziegler-Katalysator aus Neodymversatat, Ethylaluminiumsesquichlorid und Triisobutylauminium wurde untersucht. Die Polymerisationsgeschwindigkeit wurde durch Dichtemessungen verfolgt. Zur Beschreibung der Polymerisationskinetik bei verschiedenen Katalysatorzusammensetzungen wurde ein mathematisches Modell entwickelt. Bei einem molaren Aluminium/Neodym-Verhältnis über 40 kann mittels Gelpermeationschromatographie eine bimodale Molmassenverteilung beobachtet werden, was zu der Annahme führt, daß im Polymerisationssystem mehr als eine aktive Spezies anwesend ist.
    Notes: The batch polymerization of butadiene in hexane with an in-situ-activated Ziegler-Catalyst containing neodymium versatate, ethylaluminium sesquichloride and triisobutylaluminium was studied at 45°C. The rate of polymerization was determined by online density measurements. A mathematical model has been developed which is able to describe the kinetics of polymerization at different catalyst ratios. At molar ratios of aluminium/neodymium above 40 a bimodal molar mass distribution can be observed by gel permeation chromatography which leads to the assumption of more than one active species being present in the polymerization system.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 32
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 206 (1993), S. 1-9 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Fähigkeit von zwei Polymeren zur Adsorption von Escherichia coli (E. coli) in sterilisierter physiologischer Kochsalzlösung wurde untersucht. Als Polymere wurden die Reaktionsprodukte von unlöslichen Poly(glycidylmethacrylat)-Kügelchen (PGMA) mit Tetraethylenpentamin (TEP) bzw. Polyethylenimin mit einem Molekulargewicht von 60 (PEI600) verwendet. Die Zahl der vermehrungsfähigen Zellen nahm in Gegenwart dieser Polymeren ab. Elektronenmikroskopisch konnte nachgewiesen werden, daß diese Abnahme durch Adsorption der Bakterien auf der Polymeroberfläche verursacht wird. Die Koeffizienten (D) der Abnahme der vermehrungsfähigen Zellen (E. coli) betragen 53 und 62 ml g-1 h-1 für PGMA-TEP bzw. PGMA-PEI600. Sie werden mit den Koeffizienten bereits untersuchter Polymerer verglichen.
    Notes: A study was made of the removal of Escherichia coli (E. coli) from water by systems based on insoluble poly(glycidyl methacrylate)-g-tetraethylenepentamine and -g-polyethylenimine, i.e., the reaction products of insoluble poly(glycidyl methacrylate) (PGMA) beads with tetraethylenepentamine (TEP) or polyethylenimine having molecular weights of about 600 (PEI600). The polymers (PGMA-TEP and PGMA-PEI600) were brought into contact with E. coli in sterilized physiological saline. These polymers made the viable cell numbers decrease in this medium. It was confirmed by observation of polymer surfaces with a scanning electron microscope that this decrease was caused by adsorption of the bacterial cells onto these polymers. The decrease coefficients of viable cell numbers (D) for E. coli by these polymers were 53 ml g-1 h-1 for PGMA-TEP and 62 ml g-1h-1 for PGMA-PEI600, being compared with D by other polymers studied previously.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 33
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 206 (1993), S. 11-20 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Dehydrochlorierungsgeschwindigkeit von PVC in Gegenwart von Gummisamenöl (RSO), epoxydiertem Gummisamenöl (ERSO) sowie Metallseifen der daraus hergestellten Fettsäuren wurde unter Stickstoff gemessen. Die Anfangsgeschwindigkeiten der Dehydrochlorierung und die Zeit bis zu einem Abbauumsatz von 1% zeigen einen stabilisierenden Effekt der RSO-Derivate mit der Reihenfolge ERSO-Metalseifen 〈 RSO-Metalliseifen 〈 ERSO 〈 RSO.
    Notes: Dehydrochlorination rates of PVC in nitrogen atmosphere were determined in the presence of rubber seed oil (RSO), epoxidized rubber seed oil (ERSO), barium soap of rubber seed oil fatty acids and barium soap of epoxidized fatty acid of rubber seed oil. The initial rates of dehydrochlorination and the time required for the degradation to attain 1% conversion showed that the rubber seed oil derivatives exert a stabilizing effect on the degradation of PVC. The order of the stabilizing effect was found to be metal soaps of ERSO 〈 metal soaps of RSO 〈 ERSO 〈 RSO.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 34
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 206 (1993), S. 21-38 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: To improve materials performance like the temperature of deformation under flexural load of thermoplastic polyurethanes (TPU) blending with thermoplastics is sensible. A good compatibilization and phase adhesion of thermodynamical incompatible blend-components can be achieved by the use of the right coupling agents. In the case of blends with TPU and PA6 diisocyanate is given into the melt during the extrusion. Through the chemical reactions effects of compatibilization are achieved in the cases of blends with polyesterpolyurethanes and PA6 produced by extrusion and injection moulding and by reactions in solution, too. These could be perceived as consequence of MDI-initiated reactions within the phase boundary layer. The possible reactions with the PA6-phase will be discussed by the use of a model-system made in solution. No effects of compatibilization by MDI could be proved in the polyetherpolyurethan/PA6-system. The chemical characterization of the blends was realized by GPC and FTIR whereas the properties of the morphology are proved with the help of DSC, DMA and transmission electron microscopy (TEM).
    Notes: Zur Verbesserung der Werkstoffeigenschaften von thermoplastischen Polyurethanen (TPU), wie etwa der Wärmeformbeständigkeit, ist es sinnvoll, ein Blending mit Thermoplasten vorzunehmen. Eine gute Phasenverträglichkeit und Phasenhaftung bei thermodynamisch unverträglichen Blendkomponenten kann durch geeignete reaktive Koppler erreicht werden. Bei den Blends aus TPU and PA6 wird Diisocyanat während der Extrusion in der Schmelze eingebracht. Durch die ablaufenden chemischen Reaktionen werden bei extrudierten und verspritzten Blends und bei aus der Lösung erzeugten Systemen aus Polyesterpolyurethan und PA6 verträglichkeitsverbessernde Wirkungen erreicht. Diese wurden als Folge von mit 4,4′-Diphenylmethandiisocyanat (MDI) initiierten Reaktionen in der Grenzschicht erkannt, wobei die möglichen Reaktionen mit der PA6-Phase anhand eines Modellsystems aus der Lösung diskutiert werden. Bei Blends aus Polyetherpolyurethan und PA6 wurde keine Verträglichkeitsvermittlung durch MDI nachgewiesen. Die chemische Charakterisierung der Blends erfolgte durch GPC und FTIR, während die morphologischen Eigenschaften mittels DSC, DMA und Elektronenmikroskopie dokumentiert wurden.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 35
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 206 (1993), S. 39-52 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Reaktion von 4,9-Dioxa-1,12-dodecandiamin (DDDD) mit dem Diglycidylether von Bisphenol A (DGEBA) wurde mittels isothermer und dynamischer Differentialkalorimetrie untersucht. Die Enthalpie der Reaktion einer Epoxygruppe mit einem Amin-Wasserstoff wurde zu 112 ± 5 kJ/mol bestimmt.Die Gültigkeit eines kinetischen Modells wurde bestätigt. Es beinhaltet zwei konkurrierende Mechanismen: zum einen die Katalyse durch Hydroxy-Gruppen, die entweder an die Epoxykette gebunden sind oder während der Reaktion gebildet werden (Aktivierungsenergie 77 ± 5 kJ/mol), zum anderen eine nicht katalysierte Reaktion mit einer höheren Aktivierungsenergie (103 ± 3 kJ/mol).Eine Gelierung beeinflußt die Kinetik der isothermen Härtung nicht. Aus den Gelzeiten wurde die Bruttoaktivierungsenergie ermittelt (62 ± 2 kJ/mol).
    Notes: The reaction between the diglycidylether of bisphenol A (DGEBA) and 4,9-dioxa-1,12-dodecanediamine (DDDD) has been studied by means of isothermal and dynamic differential scanning calorimetry. The enthalpy of the reaction of an epoxy group with an amino-hydrogen has been determined to be 112 ± 5 kJ/mol. A kinetic model has been validated. It involves two competitive mechanisms: one is catalysed by the hydroxy groups initially present on the epoxy chain or generated during the reaction (activation energy 77 ± 5 kJ/mol), the other is not catalysed with a higher activation energy (103 ± 3 kJ/mol).For each isothermal curing, the kinetics are not modified by gelation. Evaluated from the gel times, the overall activation energy of the reaction is equal to 62 ± 2 kJ/mol.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 36
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 206 (1993), S. 63-68 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Durch Grenzflächen-Polykondensation von N,N′-bis(4-hydroxyphenyl)pyromellitsäurediimid mit Dichloriden verschiedener Phosphoramide wurden flammhemmende Polymere erhalten. Diese wurden mittels IR- und 1H-NMR-Spektroskopie und Elementaranalyse charakterisiert. Thermische Stabilität und Entflammbarkeit wurden thermogravimetrisch bzw. durch Bestimmung des Sauerstoff-Indexes untersucht.
    Notes: Flame-retardant poly(pyromellitic imide aryl phosphoramide-ester)s were synthesized by interfacial polycondensation of N,N′-bis(p-hydroxyphenyl)pyromellitic diimide with aryl phosphoramidic dichlorides. The polymers were characterized by IR and 1H-NMR spectroscopy. The molecular composition was confirmed by elemental analysis. The thermal stability and flammability of the polymers were studied by thermogravimetry and limiting oxygen index, respectively.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 37
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Der Einfluß von Zusammensetzung und chemischer Struktur auf die thermischen Eigenschaften von Polyimiden aus handelsüblichen Allyl-„Nadimid“-Harzen und Phosphor enthaltenden “Nadimid”-Harzen wurde untersucht. Thermogravimetrische Messungen unter Stickstoff an Harzen, die 1 h bei 300 gehärtet wurden, ergaben eine Erhöhung der thermischen Stabilität.
    Notes: The effect of composition and chemical structure of addition polyimides on thermal characteristics was investigated using commercially available allyl nadic-imide resins and phosphorus-containing nadimide resins. Thermogravimetric analysis, in N2 atmosphere, of resins cured at 300°C for 1 h revealed improvement of thermal stability.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 38
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Polyethylenglykol-Makromonomere mit Methacryloyl-Endgruppen wurden in Gegenwart von 2,2′-Azo(N,N′-dimethylenisobutyramidin) in einem Ethanol/Wasser-Gemisch (4:1, v/v) bei verschiedenen Temperaturen mit Styrol copolymerisiert. Die Gesamtaktivierungsenergie dieser Dispersionscopolymerisation beträgt 48 kJ/mol.
    Notes: Copolymerization of poly(ethylene glycol) macromonomers with terminal meth-acryloyl groups with styrene was carried out in the presence of 2,2′-azobis(N,N′-dimethyleneisobutyramidine) in ethanol/water mixture (4:1, v/v) at various temperatures. The overall activation energy for the dispersion copolymerization was obtained as 48 kJ/mol.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 39
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 212 (1993), S. 147-155 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Magnetische Zellulosepartikel wurden aus Viskose und Eisenpulver mit einer den thermischen Sol-Gel-Übergang nutzenden Suspensionsmethode hergestellt. Die so erhaltenen Teilchen konnen mit einem von außen angelegten, rotierenden Magnetfeld eines üblichen Permanentmagneten durchmischt werden. Die Abtrennung der Partikel von der Reaktionssuspension sollte in einer dünnen Schicht des Materials durch ein starkes Magnetfeld erfolgen. Magnetische Zellulosepartikel, die mit einer SmCoFe-Legierung anstelle des Ferrits hergestellt wurden, besitzen bessere magnetische Eigenschaften.
    Notes: Mangetic bead cellulose was prepared from viscose and ferrite powder by employing the suspension procedure using the thermal sol-gel transition. The particles thus obtained can be stirred if acted upon by an external rotary magnetic field of a common permanent magnet. Isolation of the particles from reaction suspensions should proceed in a thin layer using a strong magnetic field. Magnetic bead cellulose prepared from supermagnetic powder of the SmCoFe alloy shows a better behaviour in the magnetic field than ferrite materials.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 40
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 212 (1993), S. 103-119 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Unterschiedliche Methoden zur Messung der thermo-oxidativen Stabilität von Polypropylen wurden verglichen. Die Induktionszeiten des oxidativen Abbaus wurden mittels Differentialkalorimetrie (DSC) zwischen 160 und 240°C bis zu 10000 min gemessen. Die gleichen Proben wurden bei 130 bis 160°C 13000 h einer Alterung im Heizofen ausgesetzt.Unterschiedlich stabilisierte Proben ergaben bei dynamischen DSC-Messungen unterschiedliche Ergebnisse. Die Übereinstimmung zwischen dynamischen und statischen Experimenten waren bei kleinen Heizraten am besten.Die Arrhenius-Diagramme der isothermen DSC-Messungen unterscheiden sich von denen der Alterungsversuche; die erhaltenen Geraden schneiden sich entweder in der Nähe der Polypropylen-Schmelzpunkte oder verschieben sich bei den durch Temperung gealterten Proben zu längeren Zeiten. Die scheinbaren Aktivierungsenergien aus den Ofen-Temperungsmessungen sind sehr vie1 niedriger als die aus den DSC-Messungen berechneten und liegen bei allen Proben in einem einheitlichen Bereich, während bei den DSC-Experimenten ein Einfluß des Stabilisators zu erkennen ist.Die thermische Stabilität von Polypropylen wird auch von Antistatika und Farbpigmenten beeinflufßt. Besonders Rot-Pigment wirkt als Stabilisator für Polypropylen, was aus den Ofen-Alterungsversuchen hervorgeht; es verliert diesen Effekt aber bei höheren Temperaturen.
    Notes: The correlation between different methods of measuring thermo-oxidative stability of polypropylene has been studied. The oxidation induction times were measured using differential scanning calorimetry (DSC) in the temperature range from 160°C to 240°C up to 10000 min. The same samples were oven-aged in the temperature range from 130°C to 160°C up to 13000 h.The dynamic experiments performed by DSC show different results for differently stabilized samples. At slow heating rates the results of the dynamic experiments corresponded best to the results of the isothermal experiments.The straight-line Arrhenius plots of the isothermal DSC measurements do not correlate with the straight-line Arrhenius plots of the oven-aging tests. The Arrhenius plots obtained by these two methods either intersect close to the melting temperature of polypropylene or show jumps towards longer times when switching from DSC to oven-aging. It was found that the apparent activation energies obtained from the oven-aging tests are much lower than these obtained by DSC measurements. Almost the same activation energies were obtained for all the samples in oven-aging, while for the differently stabilized samples the activation energies from DSC measurements showed different results.Antistatic additives and colour pigments influence the thermal stability of polypropylene. Especially red pigment acts like a stabilizer for polypropylene, which is noticed at oven-aging testing, but at higher temperatures it loses this stabilizing effect.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 41
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 212 (1993), S. 201-202 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 42
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 207 (1993), S. 31-41 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Aktiviertes Aluminiumoxid wurde mit den Produkten der Reaktionen von chlormethyliertem Polystyrol mit Diethylamin, von Poly(styro1-co-chlormethylstyrol) mit Diethanolamin und von Poly(styro1-co-glycidylmethacrylat) mit Diethanolamin belegt und zur Adsorption von Escherichia-coli-Bakterien aus Wasser eingesetzt. 100 mg belegtes Trägermaterial wurden mit einer E.-coli-Suspension (20 ml, 107-8 Zellen/ml) gerührt, wobei die Zahl der lebensfähigen Zellen durch Adsorption abnahm; das Adsorptionsgleichgewicht wurde nach etwa 2 h erreicht. Der Abnahme-Koeffizient D (entspricht der Adsorptionsgeschwindigkeitskonstante) wurde aus der Abnahme der Zahl der lebensfähigen Zellen nach 2 h Adsorption gemessen.
    Notes: Reaction products of soluble chloromethylated polystyrene with diethylamine, poly(styrene-co-chloromethylstyrene) with diethanolamine, and poly(styrene-co-glycidyl methacrylate) with diethanolamine were prepared and supported on activated alumina granules. A study was made of removal of Escherichia coli cells from water by these supported alumina granules. When these granules (0.100 g) were stirred in a viable cell suspension (107-8 cells/ml, 20 ml), the viable cell number decreased by the adsorption of the cells to the granules. The adsorption attained approximately to the equilibrium (saturated adsorption) after about 2 h from the start of the adsorption. The decrease coefficient (D, which corresponds to the adsorption rate constant) was determined from the decrease in the viable cell number in the adsorption for about 2 h from the start.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 43
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 207 (1993), S. 43-52 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die radikalische Polymerisation von Bisphenol-S enthaltenden Mono- und Dimethacrylsaureestern (BPS-M und BPS-DM) wurde bezüglich Polymerisationsgeschwindigkeit, Läsungsmitteleinfluß, Copolymerisation und Kinetik der Photovernetzung untersucht. Es zeigte sich, daß das Lösungsmittel die Polymerisationsgeschwindigkeit signifikant beeinflußt; polare Lösungsmittel wie DMSO und Acetonitril verlangsamen die Polymerisationsgeschwindigkeit. Die Copolymerisation von BPS-M (M1) mit MMA (M1) wurde in Aceton bei 60°C untersucht. Die Copolymerisationsparameter wurden nach der Fineman-Ross-Methode zu r1 = 3,72 ± 0,0l und r2 = 0,80 ± 0,0l berechnet. Die hohe Reaktivität von BPS-M in diesem Copolymerisationssystem kann vermutlich dem „Matrix-Effekt“ zugeschrieben werden. Funktionelle Polymere mit Methacrylat- Seitengruppen wurden erfolgreich modifiziert und durch Bestrahlung in Gegenwart von Benzoinisopropylether photovernetzt. Die Kinetik der Photovernetzung ist zweiter Ordnung.
    Notes: Radical polymerizations of mono- and di-methacrylic esters containing bisphenol-S (BPS-M and BPS-DM) were studied in terms of polymerization rate, solvent effect, copolymerization and kinetic measurements of photocrosslinking. The solvents were found to affect significantly the polymerization rate. Polar solvents such as DMSO and acetonitrile were found to slow down the polymerization rate. Copolymerization of BPS-M(M1) with MMA(M2) was studied in acetone at 60°C. The monomer reactivity ratios were calculated to be r1 = 3.72 ± 0.01 and r2 = 0.80 ± 0.01 by the Fineman-Ross method. The high reactivity of BPS-M observed in this copolymerization system may be due to the “matrix effect”. Functional polymers containing methacrylate side-groups were successfully modified and photocrosslinked by irradiation in the presence of benzoin isopropyl ether. The photocrosslinking process is found to be of second order kinetics.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 44
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Reaktion von Chlorsilanen (Me3SiCl, R2SiCl2, SiCl4; R=Me, Ph) mit MgCl2 · 6 H2O wurde bezüglich der Entfernung des Kristallwassers untersucht. Die Dehydratisierungsgeschwindigkeit hängt von der Art des Chlorsilans ab. Bei der Reaktion mit Dichlordiphenylsilan entsteht in hoher Ausbeute ungelöstes, wasserfreies Magnesiumchlorid, das als Trägermaterial für die Herstellung eines Titan-Katalysators verwendet wurde. Dieser zeigt mit Et3Al und Ph2Si(OMe), als Cokatalysatoren eine hohe Aktivität für die Propylenpolymerisation.
    Notes: Reaction of chlorosilanes (Me3SiCl, R2SiCl2, SiCl4; R=Me, Ph) with MgCl2 · 6 H2O were investigated for the efficiency of removal of water. The nature of chlorosilane is found to govern the rate of dehydration. The treatment of hydrated magnesium chloride with dichlorodiphenylsilane gives unsolvated anhydrous magnesium chloride in high yields. Anhydrous MgCl2 is used as support for the preparation of titanium catalyst. The catalyst in conjunction with Et3Al and Ph2Si(OMe)2 as cocatalyst system shows high activity for propylene polymerization.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 45
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Es wird die Synthese verschiedener, mindestens bifunktioneller Azoverbindungen und deren Einbau in eine Polymerhauptkette mittels Grenzflächenpolykondensation beschrieben. Die thermischen und photochemischen Eigenschaften von Modellverbindungen sowie der Polymeren wurden durch UV-Spektroskopie und DSC-Messungen untersucht. Mit Hilfe von Viskositätsmessungen wurde der Kettenabbau eines Azopolymeren nachgewiesen.
    Notes: The synthesis of new, unsymmetrically functionalized azo compounds and their incorporation into polymers is described. Their photochemical decomposition and thermal stability was studied by UV spectroscopy and differential scanning calorimetry (DSC), respectively. Chemical degradation was followed by viscosity measurements.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 46
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 207 (1993), S. 173-186 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Durch Phasengrenzflächenpolykondensation von 4,4′-Dimercaptobiphenyl mit ausgewählten aliphatischen und isomeren Phthalsäuredichloriden wurden neue Polythioester erhalten. Um die optimalen Bedingungen der Phasengrenzflachenpolykondensation zu bestimmen, wurde der Einfluß folgender Faktoren auf die reduzierte Viskosität und Ausbeute der Polythioester ermittelt: Art der organischen Phase, Konzentration der Reagenzien, Verhältnis der wässrigen zur organischen Phase, Art und Konzentration des HC1-Akzeptors, Reaktionstemperatur und -zeit. Die Polykondensation von Dithiol mit Isophthalsäuredichlorid wurde als Modellsystem speziell untersucht. Die Polythioesterstrukturen wurden mittels Elementaranalyse, IR-Spektroskopie und Riöntgenspektroskopie bestimmt. Aus der thermogravimetrischen Analyse wurden die Anfangszersetzungstemperatur, die Gewichtsabnahme bei dieser Temperatur und das Maximum der Zersetzungsgeschwindigkeit erhalten. Es wurden weiterhin einige physikalisch-chemische, mechanische und dielektrische Eigenschaften ermittelt. Aufgrund der geringen Löjslichkeit der Polythioester konnten die mittleren Molekulargewichte nicht bestimmt werden.
    Notes: New polythioesters were obtained by interfacial polycondensation of 4,4′-dimercaptobiphenyl with selected aliphatic and isomeric phthaloyl dichlorides.To determine the optimum polycondensation conditions, the influence of the following factors on reduced viscosity and yield were studied: type of organic phase, concentration of hydrogen chloride acceptor, type of catalyst, reaction temperature and rate of acid dichloride addition.A thorough examination was carried out only for the polycondensation of dithiol with isophthaloyl dichloride chosen as a model system. The structures of polythioesters were determined by elemental analysis, X-ray and infrared spectra. The temperature of initial decomposition, the percentage of its mass loss, and temperature of the fastest decomposition process were determined from curves of differential and thermogravimetric analysis.Some physicochemical, mechanical and electrical properties were determined. The molecular weights were not measured because of the low solubility of the obtained polythioesters.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 47
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 207 (1993), S. 215-216 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 48
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die negativ geladene Oberfläche von feindispersen anorganischen Materialien wie Kieselgur, Perlit, Kaolin oder Glas kann durch die Adsorption von kationischen Polyelektrolyten umgeladen werden. Bei hohen Mengen an adsorbiertem Polykation besitzen die Oberflächen der unterschiedlichen Materialien dann gleiche elektrokinetische Eigenschaften. An den derart modifizierten Grenzflächen können anionische Farbstoffe adsorbiert werden. Bei Zugabe eines Polyanions, resultierend in der Bildung eines Polyelektrolytkomplexes, kann die Zahl der kationischen Zentren in der Grenzfläche und damit die Adsorptionskapazität für den Farbstoff erhöht werden. Die experimentellen Resultate deuten darauf hin, daß das Zetapotential bestimmt wird durch die außeren Bereiche der PEC-Schicht, wahrend die Farbstoffadsorption auch durch die inneren Regionen der Oberfläche mitbestimmt wird. Unmittelbar nach der Modifizierung mit Poly(diallyldimethylammoniumchlorid) und Poly(maeinsäure-co-α-methylstyrol) besitzen die modifizierten Materialien bei einem hohen Überschuß des Poly-anions ein negatives Zetapotential, aber ein positives nach der Abtrennung der überstehenden Lösung. Dieses Verhalten steht in Übereinstimmung mit der Bildung eines nichtstochiometrischen PEC mit Polykation im Überschuß und einer reversiblen Wechselwirkung mit überschüssigem Polyanion in der Lüsung. Die Ergebnisse deuten an, daß die Oberflache als fest-analoger Polyelektrolyt in Konkurrenz zu dem Polyanion an der Reaktion beteiligt ist.
    Notes: The surface charge of inorganic finely dispersed materials like diatom earth, perlite, glass or clay may be changed from negative to positive by the adsorption of cationic polyelectrolytes. Different materials exhibit equivalent electrokinetic surface properties with high amounts of the polycation adsorbed. Interfaces modified this way are able to adsorb anionic dye stuffs. Their adsorption capability for the dye stuff may be enhanced by addition of polyanions due to the formation of a nonstoichiometric polyelectrolyte complex (PEC) and therefore an increased number of cationic centres in the interface. Experimental results indicate that the zeta potential is correlated to the outer PEC layer whereby dye stuff adsorption measurements are sensitive for the more inner surface regions, too. Immediately after modification, materials modified with poly(diallyldimethylammonium chloride) and poly(maleic acid-co-α-methylstyrene) have negative zeta potentials at high excess of added polyanion and a positive one after separation of the solid. This behaviour is attributed to the formation of a nonstoichiometric PEC with polycation in excess and reversible interaction with polyanion in the surrounding solution. Experimental results indicate that the surface may act as “solid-like” polyelectrolyte in competition to the polyanion.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 49
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 207 (1993), S. 195-202 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die dielektrischen Relaxationsprozesse in Sulfobetain-Polyurethanionomeren mit Polyethersegmenten (Co2+ -komplexierte und H,S-behandelte Formen) wurden mit der TSDC-Methode untersucht und mit denen nichtionischer Polyurethane und verwandter Verbindungen verglichen. Vier mit c, βs, β′ und βh bezeichnete Relaxationsprozesse wurden in Polyurethanionomeren im Temperaturbereich von 110 bis 370 K beobachtet und mit möglichen molekularen Bewegungsprozessen korreliert. Die Einflüsse des Gehalts an Hartsegmenten, der Komplexierung sowie der H2S-Behandlung auf die Relaxationsprozesse wurden unter Berücksichtigung der strukturellen Modifikationen der harten und der weichen Mikrophasen erklärt.
    Notes: Dielectric relaxation processes in sulfobetaine polyurethane ionomers based on polyether, were studied comparatively to nonionic polyurethane and related compounds with Co2+ (complexed and H2S-treated forms) by using thermally stimulated depolarization currents (TSDC).Four relaxation processes denoted as γ, βs, β′ and βh in polyurethane ionomers over the 110-370 K range were observed. Molecular origin of these processes was suggested. The effects of the hard segments content, complexation and H2S treatment on the relaxation processes were explained in terms of the structural modifications of the hard and soft microphases.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 50
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Komplexierung von Co(II), Ni(II), Cu(II), Zn(II) und Hg(II) in Amin-funktionalisierten, mit N-(Acrylamidomethyl)acrylamid (NNMBA) vernetzten Polyacrylamiden wurde untersucht. Die Metallionenaufnahme hängt vom Vernetzungsgrad ab und nimmt in der Reihenfolge Hg(II) ≫ Cu(II) 〉 Zn(II) 〉 Ni(II) 〉 Co(II) ab. Die Kinetik der Komplexierung ist erster Ordnung. Die Metallkomplexe wurden mittels IR- und EPR-Spektroskopie charakterisiert. Die Harze können ohne Kapazitätsverlust nach Dekomplexierung mehrmals verwendet werden; die desorbierten Harze komplexieren bevorzugt das vorher gebundene Metallion. Das Quellvermögen der komplexierten ist geringer als das der nichtkomplexierten Harze und hängt vom Vernetzungsgrad ab.
    Notes: The complexation of amino functions supported on poly(acrylamides) with 2-20 mol-% of N-(acrylamidomethyl)acrylamide (NNMBA) crosslinks towards Co(II), Ni(II), Cu(II), Zn(II), and Hg(II) ions was investigated. The metal ion uptake was found to be dependent on the extent of the NNMBA crosslinking. The observed trend in complexation is Hg(II) ≫ Cu(II) 〉 Zn(II) 〉 Ni(II) 〉 Co(II). The kinetics of complexation was found to be of first order. The derived metal complexes were characterised by IR and EPR. The complexed resins can be recycled several times without capacity loss. The metal-desorbed resins showed specificity to the metal ion which was initially present. The extent of swelling of the complexed resins is lower than that of the uncomplexed resins and it varies with the extent of crosslinking.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 51
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 208 (1993), S. 17-23 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die elektrische Leitung von mit verschiedenen Übergangsmetallen (Fe, Co, Cu, Cr) dotiertem Polycarbonat (PC) wurde im Temperaturbereich von 293 bis 493 K untersucht. Die Leitfähigkeit von PC mit FeCl, war siebenmal höher als jene der anderen Proben. Die effektive Potentialschwelle Φ wurde zu 0,2 eV berechnet. Weiterhin wurde die Dielektrizitätskonstante bei verschiedenen Temperaturen untersucht.
    Notes: The electrical conduction of polycarbonate (PC) doped with different transition metals was studied in the temperature range of 293-493 K. The conductivity of PC doped with FeCl3 is 7 orders higher in comparison with the other samples. The effective potential barrier (Φ) for pure PC was calculated (0.2 eV). Also, the dielectric constant at different temperatures was studied.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 52
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 208 (1993), S. 25-38 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Wirkung von Lichtstabilisatoren im ersten Stadium der Alterung von Polyethylen niedriger Dichte (LDPE) wurde mit elektrischen Methoden untersucht. Drei verschiedene UV-Stabilisatoren wurden verwendet: ein Phosphit-Derivat (3,9-Bis[(2,4-di-tert-butyl)phenoxy]-2,4,8,l0-tetraoxa-3,9-diphosphaspiro[5.5]undecane), ein Benzophenon-Derivat (2-Hydroxy-4-octyloxybenzophenon) und ein Chelat [2,2′-Thiobis(4-tert-octylphenolato)(n-butylamino)nickel(II)]. Diese Stabilisatoren, speziell das Chelat, verbesserten die UV-Stabilität von LDPE für elektrische Anwendungen.
    Notes: The efficiency of light stabilizers is investigated by electric methods in the initial stage of photooxidative ageing of low density polyethylene (LDPE). Three types of UV light stabilizers are tried to improve the UV stability of LDPE: a phosphite type (3,9-bis-[(2,4-di-tert-butyl)phenoxy]-2,4,8,10-tetraoxa-3,9-diphosphaspiro[5.5]undecane) a benzophenone type [2-hydroxy-4-octyloxy-benzophenone] and a stabilizer based on chelate salt [2,2′-thiobis(4-tert-octyl phenolato) (n-butylamine) nickel (II)]. LDPE is very susceptible to ultraviolet light. UV light stabilizers improve the stability of low density polyethylene for electrical applications, especially the UV stabilizer based on chelate salt.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 53
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 208 (1993), S. 39-46 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Ein Poly(vinylalkohol)-Film (PVA) wurde nach Erhitzen in siedendem Wasser gequollen und durch Bestrahlen mit Elektronen vernetzt. Das so erhaltene PVA-Hydrogel weist eine höhere Elastizität und bessere mechanische Eigenschaften auf, obwohl es noch quellbar ist. Das Volumen des vernetzten Hydrogels reagiert sehr empfindlich auf einen Wechsel des Quellungsmittels und eine Temperaturänderung. Nach Kontraktion durch Eintauchen in Aceton nimmt die Zugfestigkeit zu. Durch wiederholtes Erhitzen des Hydrogels in siedendem Wasser und anschließendes Abkühlen wurden Kontraktions-Quellungs-Zyklen durchlaufen. Bei Temperaturen oberhalb 40°C nimmt das Quellungsverhältnis stark ab.
    Notes: Responsive poly(vinyl alcohol) PVA hydrogels obtained by electron irradiation after heating of a water-swollen film show higher elasticity and tougher properties even after boiling in water, although some swelling did occur. The volume of the hydrogel after boiling was very sensitive to solvent (acetone) and temperature. The crosslinked hydrogels show higher tensile strength after rapid contraction by immersion in acetone. The crosslinked PVA was boiled and cooled to induce contraction and swelling cycles. The swelling ratio of hydrogel decreased remarkably at temperatures higher than 40°C.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 54
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 208 (1993), S. 65-77 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Umsetzung von 2,2′,6,6′-Tetrabrombisphenol A (TBBPA) mit Phosgen in einer mit Trialkylamin katalysierten Grenzflächenpolykondensation liefert nur Polymere mit niedrigem Molekulargewicht. Die geringe Reaktivität von TBBPA wird auf dessen sterisch anspruchsvolle Struktur und den elektronenziehenden Charakter der o-Bromsubstituenten zurückgeführt. Aus der Bildung von Carbamaten bei der Reaktion einer Modellverbindung (2,4,6-Tribromophenylchlorformat, TBPC) mit Trialkylaminen geht hervor, daß durch Zerfall des Katalysator-TBPC-Komplexes die Polymerisation abgebrochen wird. Das Carbamat wird durch Zersetzung des Acylammoniumsalzes gebildet, wobei eine nucleophile Substitution durch das Chloridion an dem an das positiv geladene Stickstoffatom gebundenen Kohlenstoffatom stattfindet.
    Notes: 2,2′,6,6′-Tetrabromobisphenol-A (TBBPA), a sterically hindered bisphenol, is known to give only low-molecular-weight polymers using the interfacial phosgenation process. The low reactivity is attributed to the bulkiness and electron-withdrawing character of bromine substituents at the ortho positions. From the formation of carbamate products in model compound (2,4,6-tribromophenyl chloroformate, TBPC) reactions with trialkylamines, the trialkylamine catalyst was found to act as a terminator by the degradation of the chloroformate-trialkylamine complex. The generation of carbamate occurs through the decomposition of the acyl ammonium salt proceeding via nucleophilic displacement by Cl- at the carbon attached to the positive nitrogen center. The relative catalytic abilities of trialkylamines and pyridine derivatives were determined in the homogeneous (dichloromethane) and interfacial (dichloromethane/water) systems. From the results of model reactions with TBPC and sodium tribromophenolate, 4-dimethylaminopyridine (DMAP) was found to be the best catalyst.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 55
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 208 (1993), S. 47-64 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die thermische Alterung von extrudierten Proben von mit Elektronenstrahlen vernetztem linearem Polyethylen wurde im Temperaturbereich von 110-170°C untersucht. Kurz- und langfristige Veränderungen der mechanischen (Dehnungs-)Eigenschaften wurden beobachtet; die entsprechenden Alterungsmechanismen werden auf der Basis ergänzender Sol-Gel-, Dichte-, FTIR- sowie gravimetrischer Messungen und Zugversuche an Mikrotomschnitten diskutiert.Zwei Mechanismen führen zu kurzfristigen Eigenschaftsänderungen: eine Nachvernetzung und eine Änderung der Kristallstruktur (bei Proben oberhalb ihrer Schmelztemperatur). Im vorliegenden Fall wurden die Polymeren im festen Zustand vernetzt, so daß die Änderung der Kristallstruktur zu einer erkennbaren Abnahme der Streckspannung (ca. 5 MPa) führte.Die langfristigen Veränderungen treten nach dem Ende der Oxidationsinduktionsperiode auf. Sie können als Übergang vom zähen in den spröden Zustand interpretiert werden, der durch Strukturänderungen sowohl auf molekularer (durch Kettenspaltung) als auch makroskopischer Ebene (durch diffusionskontrollierte Kinetik der Oxidation verursachte Kern-Schale-Struktur) hervorgerufen wird. Durch IR- und DSC-Analysen wurde festgestellt, daß wahrnehmbare Änderungen in der Dehnung erst kurz vor dem Ende der Induktionsperiode auftreten.
    Notes: The thermal aging of extruded samples of electron beam-crosslinked linear polyethylene has been studied in the 110-170°C temperature range. Short and long term changes of mechanical (tensile) properties were observed, and the corresponding mechanisms are discussed on the basis of complementary sol-gel and gravimetric measurements on whole samples, and density, FTIR and tensile testing on microtome sections.Two mechanisms are involved in short term changes: a post-crosslinking and a change of the crystalline morphology (for samples exposed above the melting point). The latter effect is especially important in the case under study where the polymer was crosslinked in the solid state and leads to a noticeable decrease (∼5 MPa) of the yield stress.The long term changes take place after the end of the induction period of oxidation. They can be interpreted in terms of ductile-brittle transition induced by structural changes occurring on the macromolecular level (chain scission) as well as macroscopically (core-shell structure resulting of the diffusion control of oxidation kinetics). It appears that noticeable changes of ultimate elongation occur just before the end of the induction period as detected by IR or DSC method.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 56
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 209 (1993), S. 95-109 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Poly(epichlorhydrin) wurde durch nukleophile Substitution mit aliphatischen Kaliumcarboxylaten mit endstandigen Doppelbindungen (10-Undecenoat, 4-Pentenoat und 3-Butenoat) modifiziert. Die Reaktionsbedingungen wurden variiert, um ihren Einfluß auf den erreichten Substitutionsgrad zu untersuchen. Die hergestellten Polyether wurden mittels Elementaranalyse, spektroskopischen und thermischen Methoden sowie Viskositäts- und osmometrischen Messungen charakterisiert. Es wurde sowohl eine geringe Vernetzung als auch die bereits bekannte Hauptkettenspaltung beobachtet. Während der Substitutionsreaktion isomerisierte das Vinylacetat zum Crotonsäureester.
    Notes: Poly(epichlorohydrin) was modified by nucleophilic substitution with some aliphatic potassium carboxylates containing terminal double bonds (10-undecenoate, 4-pentenoate and 3-butenoate). In order to monitor the degree of substitution achieved, different reaction conditions were tested. The polyethers obtained were characterized by spectroscopic techniques, elemental analysis, thermal methods, viscosity determinations and osmometric measurements. A slight crosslinking and the reported main chain cleavage were both detected. Finally, it must be pointed out that, during the substitution reaction with the vinylacetate, isomerization to crotonic ester took place.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 57
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 210 (1993), S. 21-32 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Polypropylen wurde mittels Gasentladung unter niedrigem Druck behandelt. Die Oberflaäachenmodifizierung wurde durch ESCA-Analysen, Messungen der Benetzbarkeit und Adhäasionsunterschungen in Abhäangigkeit von der Behandlungszeit und der Art des verwendeten Gases (Luft oder Argon) charakterisiert. Die Ergebnisse von “advancing”- und “receding” -Kontaktwinkelmessungen mit Wasser (sehr polar) und Diiodmethan (unpoler) in einem automatischen dynamischen Tensiometer ziegen eine Zunahme der Benetzbarkeit nach der Oberfläachenbehandlung. Dier wird auf die entstehung hochenergetisch polarer Stellen auf der Oberfläache zuräuckgefäuhrt. Die ESCA-Analyse belegt, daß die modifizierte Oberfläahe aud niedermolekularem Material besteht; sie ist in Methanol läolich.Die Adhäsion von Aluminium an der Polypropylen-Oberfläche wird bereits durch eine wenige Sekunden dauernde Gasentladungsbehandlung verbessert. Sie hängt von der polaren Komponente der Oberflächenenergie des Polymeren ab.
    Notes: Low-pressure discharge treatments were applied to the surface of polypropylene. ESCA analyses, wettability measurements and adhesion tests were carried out to characterize surface modifications as a function of treatment time and nature of gas (air or argon). Advancing and receding contact angles were measured with an automatic dynamical tensiometer. The liquids used were water (very polar liquid) and methylene iodide (apolar liquid). The results show an increase in wettability by the surface treatment. This is due to the creation of high-energy polar sites. ESCA analysis also shows that the modified surface layer is soluble in methanol and is made up of low-molecular-weight material.Adhesion of polypropylene/aluminium is also increased by the low pressure discharge treatment from the few first seconds of the treatment. This adhesion increase is a function of the polar component of the polymer surface energy.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 58
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Blends aus Poly-ε-caprolacton (PCL) und Polymethylmethacrylat (PMMA) wurden durch Polymerisation von Methylmethacrylat in Gegenwart von PCL hergestellt. Die thermeischen, morphologischen, dynamisch-mechanischen und mechanischen Eigenschaften der Blends wurden ermittelt. Zum Vergleich wurden Blends durch mechanisches Mischen von PCL-und PMMA-Homopolymerschmelzen hergestellt und charakterisiert. Die nach beidenMethoden hergestellten Blends unterscheiden sich wesentlich in der phasenstrukturund den mechanischen eigenschafte, was wahrscheinlich auf die bildung von gepfropften Anteilen bei der erstgenannten Methode zuräuckgefäuhrt werden kann.
    Notes: Blends of poly-ε-caprolactone (PCL) and poly(methylmethacrylate) (PMMA) were prepared by a reactive method and characterized by thermal, morphological, dynamic mechanical and mechanical analyses. For comparison, “mechanical” blends, obtained by melt-mixing of preformed polymers, have been prepared and characterized. The two series of blends are different in phase structure and in mechanical tensile properties, probably due to the formation of grafted species during reactive blending.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 59
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 210 (1993), S. 33-46 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Der Einfluß der Oberfläachenbehandlung von Säagemehl auf die physikalisch mechanischen Eigenschaften von mit Säagemehl gefäulltem Polypropylen wurde untersucht. Wäahrend mit Elastomerem beschichtetes Säagemehl die Festigkeit der Compostie veschlechtert, fäuhrt diein-situ-Addition von Oberfläachenmodifikatoren (mit Maleinsäaureanhydrid oder N-(3-Maleimidophenyl) maleimid modifiziertes Polypropylen) wäahrend des Knetens des Polypropylens mit unbehandeltem odermit Elastomerem vorbehandeltem Säagemehl zu einer Verbesserung der mechanischen Eigenschaften bei nurgeringer Beeinträachtigung der Schlagzäahigkeit. Die chemische Natur des Oberfläachenmodifikators ist dabei von besonderer Bedeutung, d.h. mit Maleinsäaurenhydrid modifiziertes Polypropylen erwies sich als der effektivste der untersuchten Modifikatoren. Halogenierte Elastomere und mit einem Phenolharz modifiziertes Polypropylen verbessern das Brandverhalten der Composite. Außerdem häangen die Eigenschaften von der Größe der Holzfasern ab. Die morphologische Untersuchung von Bruchfläachen der Composite zeigte, daß die Grenzfläachenadhäasion durch das mit Maleinsäaureanhydrid modifizierte Polypropylen verbessert wird.
    Notes: The effect of surface treatment of saw dust on the physico-mechanical properties of saw dust-filled polypropylene composites was studied. Whereas the elastomer-pretreated saw dust decreases the strength of composites, in-situ addition of interface modifiers, such as maleated polypropylene, m-phenylene bismaleimideSystematic name: N-(3-maleimidophenyl)maleimide.-modified polypropylene, during kneading of polypropylene with untreated or elastomer-pretreated saw dust improved the mechanical properties with a marginal sacrifice of impact strength. The chemical nature of interphase modifiers played an important role on the mechanical properties of the composites, e.g., maleated polypropylene was most effective among the modifiers used in this study. Halogenated elastomers and phenolic modified polypropylene improved the flame resistant properties of the composites. More over, properties varied with the particle size of wood fiber. The morphological study of the fracture surfaces of composites revealed that interfacial adhesion is improved by adding maleated polypropylene.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 60
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In order to induce a β-turn conformation into the chemotactic linear tripeptide N-formyl-L-methionyl-L-leucyl-L-phenylalanine (fMLP), the new analogue N-formyl-L-methionyl-ΔZleucyl-L-phenylalanine methyl ester [ ΔZLeu]2f MLP-OMe (1) has been synthesized. The conformational and biochemical consequences of this chemical modification have been determined. Analogue 1 has been synthesized by using N-carboxy-(Z)-α,β-didehydroleucine anhydride as key compound to introduce the unsaturated residue at the central position of the tripeptide 1. The x-ray analysis shows that 1 adopts in the crystal a type II β-turn conformation in which the new residue occupies the (i + 2) position, and an intramolecular H bond is formed between the formylic oxygen and the Phe NH. 1H-nmr analysis based on nuclear Overhauser effect measurements suggests that the same folded conformation is preferred in CDCl3 solution; this finding is also supported by molecular dynamics simulation. The biological activity of 1 has been determined on human neutrophils (polymorphonuclear leukocytes) and compared to that shown by f MLP-OMe. Chemotactic activity, granule enzyme release, and superoxide anion production have been determined. Analogue 1 is practically inactive as chemoattractant, highly active in the superoxide generation, and similar to the parent in the lysozyme release. The conformational restriction imposed on the backbone by the presence of the unsaturated residue is discussed in relation with the observed bioselectivity. © 1993 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 61
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 33 (1993) 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 62
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 33 (1993), S. 521-533 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Peptide GVKGDKGNPGWPGAPY from the triple-helix domain of type IV collagen aggregates in solution at a critical aggregation concentration of 18 mM. This molecular self association process is investigated by 1H- and 13C-nmr spectroscopy. As a function of increasing peptide concentration, selective 1H resonances are cooperatively chemically shifted by up to 0.04 ppm to apparently saturable values at high concentration. Pulsed field gradient nmr was used to derive translation diffusion constants that, as the peptide concentration is increased, also cooperatively and monotonically decrease to an apparent limiting value. An average number of 6 monomer units per aggregate have been estimated from diffusion constant and 13C relaxation data. Comparative 1H nuclear Overhauser effect spectroscopy (NOESY) spectra accumulated at high and low peptide concentrations suggest that average internuclear distances are decreased as a result of peptide association. 13C-nmr multiplet spin-lattice relaxation and 13C- {1H} NOE effects on 13C-enriched glycine methylene positions in the peptide demonstrate that overall molecular tumbling and backbone internal motions are attenuated in the aggregate state. Lowering the solution pD from pD 6 to pD 2 disrupts the aggregate state, suggesting a role for electrostatic interactions in the association process. Based on thermodynamic considerations, hydrophobic interactions also probably act to stabilize the aggregate state. These data are discussed in terms of an nmr/NOE constrained computer-modeled structure of the peptide. © 1993 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 63
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The secondary structure transformation of β-lactoglobulin from a predominantly β-structure into a predominantly α-helical one, under the influence of solvent polarity changes is reversible. Independent of the alcohol used  -  methanol, ethanol, or 2-propanol  -  the midpoints of the observed structural transformation occur around dielectric constant ε ≈ 60. The structural change destroying the hydrophobic core formed by the β-barrel structure leads, at room temperature, to the dissociation of the retinol/β-lactoglobulin complex in the neighborhood of dielectric constant ε ≈ 50. However, when the dielectric constant of the medium is raised back to ε ≈ 70 by the decrease of the temperature, both the refolding of BLG into a β-structure and the reassociation of the retinol/β-lactoglobulin complex are observed. The esterification of β-lactoglobulin carboxyl groups has two effects: on the one hand it accelerates the β-strand → α-helix transition induced by alcohols. On the other hand, the esterification of β-lactoglobulin strengthens its interaction with retinol as it may be deduced from the smaller apparent dissociation constant of retinol/methylated β-lactoglobulin complex. The binding of retinol to modified or unmodified β-lactoglobulin has no influence (stabilizing or destabilizing) on the folding changes induced by alcohol. © 1993 John Wiley & Sons, Inc.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 64
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Highly specific peptide structures can be designed by inserting dehydro residues into peptide sequences. The peptide N-Boc-L-Phe-dehydro-Phe-L-Val-L-Phe-dehydro-Phe-L-Val-OCH3, synthesized by conventional procedures, crystallizes from methanol--water mixtures at 4°C in the tetragonal space group P43 with cell parameters a = b = 13.829 ± 0.003 Å, c = 27.587 ± 0.008 Å, V = 5275.5 ± 0.2 Å3, Z = 4, dm = 1.152 ± 0.005 g cm-3, dcal = 1.150 ± 0.005 g cm-3. The overall residual factor R = 0.084 for 2342 reflections, with 2θmax = 140° using CuKα radiation. The backbone torsion angles are θ1 = -171(1)°, ω0 = 168 (1)°, φ1 = 77 (2)°, ψ1 = 41 (2)°, ωl = 169 (1)°, φ2 = -46 (2)°, ψ2 = -24 (2)°, ω2 = 179 (1)°, φ3 = -63 (2)°, φ3 = -19 (2)°, ω3 = 171 (1)°, φ4 = -67 (2)°, ψ4 = -8 (1)°, ω4 = 169 (1)°, ψ5 = -61 (1)°, φ5 = -26(1)°, ω5 = 177(1)°, ψ6 = -122 (1)°, φ6T = 26 (2)°. The peptide adopts a 310-helical conformation with three intramolecular hydrogen bonds (i + 3 → i) involving carbonyl oxygen atoms of Phe1, dehydro-Phe2, Val3, and the NH groups of Phe4, dehydro-Phe5, and Val6 with distances of 3.01 (1), 2.82 (1), and 3.09 (2) Å, respectively. The structure determination revealed that a hexapeptide with two dehydro-Phe residues at (i + 2) and (i + 5) positions generates a 310-helical conformation. The helical peptide molecules are arranged in a major helical arrangement about the 43axis. These helices are packed parallel to the c axis and form several interdigitating hydrogen bonds. The interhelix hydrogen-bonding regions are separated by van der Waals interactions involving the side chains of Phe, dehydro-Phe, and Val residues. © 1993 John Wiley & Sons, Inc.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 65
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 33 (1993), S. 687-692 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The salt bridge probe cyanogen (ethanedinitrile, C2N2; N≡C--C≡N) inhibits the bovine carbonic anhydrase (EC 4.2.1.1.) hydrolase activity toward various types of esters without significant effect on its hydrolyase activity. Two sets of pyridine derivatives that were isosteric substrates for the two activities were differentially affected. Acetazolamide and salamide are reversible inhibitors of the enzyme; only salamide affords protection of the hydrolase activity against the action of C2N2. Since each is known to bind in different positions within the active site, the selective effect of salamide may arise from its position covering one CO2 site as well as a site important for hydrolase activity. The C2N2 concentration dependence of the time course of hydrolase inhibition is consistent with the existence of a high C2N2 affinity site with slow covalent change and a second site with lower C2N2 affinity, but higher rate of covalent modification of the enzyme. © 1993 John Wiley & Sons, Inc.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 66
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 33 (1993) 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 67
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 33 (1993), S. 735-742 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Molecular dynamics (MD) simulations have been carried out for 62.5 ps on crystal structures of deoxy sickle cell hemoglobin (HbS) and normal deoxy hemoglobin (HbA) using the CHARMM MD algorithm, with a time step of 0.001 ps. In the trajectory analysis of the 12.5-62.5 (50 ps) simulation, oscillations of the radius of gyration and solvent-accessible surface area were calculated. HbS exhibited a general contraction during the simulation, while HbA exhibited a nearly constant size. The average deviations of simulated structures from the starting structures were found to be 1.8 Å for HbA and 2.3 Å for HbS. The average rms amplitudes of atomic motions (atomic flexibility) were about 0.7 Å for HbA and about 1.0 Å for HbS. The amplitudes of backbone motion correlate well with temperature factors derived from x-ray crystallography. A comparison of flexibility between the α- and β-chains in both HbA and HbS indicates that the β-chains generally exhibited greater flexibility than the α-chains, and that the HbS β-chains exhibit greater flexibility in the N-terminal and D- and F-helix regions than do those of HbA. The average amplitude of backbone torsional oscillations was about 9°, a value comparable with that of other simulations, with enhanced torsional oscillation occurring primarily at the ends of helices or in loop regions between helices. Comparison of atomic flexibility and torsional oscillation results suggests that the increased β-chain flexibility results from relatively concerted motions of secondary structure elements. The increased flexibility may play an important role in HbS polymerization. Time course analysis of conformational energy of association, hydrogen bonding and hydrophobic bonding (as calculated from solvent accessibility) shows that all three of these factors contribute to the stability of subunit association for both hemoglobins. © 1993 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 68
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 33 (1993), S. 409-436 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The diffusional motions of flexible macromolecules are analyzed with an increasingly realistic Rouse-Zimm model, i.e., by modeling the molecule as an arbitrary set of spheres connected by nearly harmonic springs. New features include (1) nearly arbitrary arrangements of spheres, (2) arbitrary arrangements of translational and torsional springs, (3) significant anharmonic corrections to the elastic potential surface, and (4) inclusion of torsional damping and various hydrodynamic cross-coupling effects (including two types of translational-rotational coupling) with no additional fitted parameters.The hydrodynamic interactions [R. F. Goldstein (1985) Journal of Chemical Physics, Vol. 83, pp. 2390-2397] contain no adjustable parameters other than temperature, viscosity, and the radii and positions of the spheres. These hydrodynamic interactions allow accurate calculations of rigid body diffusion as well as flexible motions.Given the positions, radii, and spring constant matrix, one can calculate a full set of three-dimensional diffusional modes. Because one uses an off-diagonal hydrodynamic resistance matrix instead of a diagonal mass matrix, the diffusional modes are different in structure from vacuum normal modes, and give rise to different rms motions in the laboratory frame. These hydrodynamic modes include the effects of vibrational-translational cross-coupling (i.e., motion along a vibrational coordinate may give rise to a translational force, and vice versa).The diffusional modes are used to simulate dynamic light scattering (DLS). I examine various molecules with different shapes, flexibilities, and with different scattering vectors. Radial and angular motions influence DLS decays differently. These effects are dependent upon the molecular shape (straight, bent, or curved) and type of flexibility (stretching or bending). Furthermore, small cubic corrections to the potential surface can be significant for DLS of certain geometries such as straight rods and semicircles. © 1993 John Wiley & Sons, Inc.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 69
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 33 (1993), S. 475-477 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Laminin is the most abundant noncollagenous protein in basement membranes. Its selfassembly has been studied in solution, and it has been established that calcium ions induce partially reversible aggregation. The behavior at a lipid membrane surface is of greater biological significance, but it is difficult to study quantitatively binding kinetics at a surface. The present work uses a powerful new integrated optics technique to measure the absorption and aggregation of the laminin-nidogen at a bilayer lipid membrane surface. It is found that the binding of a single layer of laminin at the lipid membrane is independent of the presence of calcium, but that the building up of multilayer laminin membranes requires calcium, and that these may not be destroyed by a calcium-complexing agent. © 1993 John Wiley & Sons, Inc.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 70
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 33 (1993), S. 511-511 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 71
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 1H, 13C, and 15N resonances of FKBP when bound to the immunosuppressant, ascomycin, were assigned using a computer-aided analysis of heteronuclear double and triple resonance three-dimensional nmr spectra of [U-15N] FKBP/ascomycin and [U-15N, 13C] FKBP/ascomycin. In addition, from a preliminary analysis of two heteronuclear four-dimensional data sets, 3JHN,Hα coupling constants, amide exchange data, and the differences between the Cα and Cβ chemical shifts of FKBP to random coil values, the secondary structure of FKBP when bound to ascomycin was determined. The secondary structure of FKBP when bound to ascomycin in solution closely resembled the x-ray structure of the FKBP/FK506 complex but differed in some aspects from the structure of uncomplexed FKBP in solution. © 1993 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 72
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The physical dimensions of several (1 → 6) branched (1 → 3) -β-D-glucan samples obtained from different organisms and their derivatives have been studied by electron microscopy, light scattering measurements, viscometry, and gel permeation chromatography. The electron micrographs indicate that in most samples these biopolymers are adequately described as linear worm-like coils. A sample reconstituted from alkaline media appeared as a blend of the linear, circular, and aggregated polymer morphologies. The average mass per unit length, ML = Mw/Lw for the macroscopically linear samples, was estimated to be 2100 ± 200 g mol-1 nm-1. The parameter mL was determined from the contour lengths obtained by electron microscopy and the molecular weight by light scattering measurements. The observed ML was consistent with the triple-helical structure reported from x-ray diffraction studies and observed degree of side-chain substitution. From the molecular snapshots shown in the electron micrographs, the persistence lengths of these β-D-glucans were determined to be 140 ± 30 nm. The experimentally determined intrinsic viscosities were consistent with these estimates of ML and persistence length. Comparison of the molecular weight distributions obtained from gel permeation chromatography and those deduced from the electron micrographs indicates that number and weight average contour lengths are more reliable than z and z + 1 averages. © 1993 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 73
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 33 (1993), S. 633-638 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The Rayleigh scattering of Mössbauer radiation has been measured on oriented hydrated fibres of A-NaDNA. The elastic and inelastic scattering intensities have been determined at different temperatures from 275 to 310 K in the Q range 0.7-3.3 Å-1. The elastic intensity has a main maximum at Q = 1.92 Å-1 due to an ordered structure of water along the DNA double helices. From the temperature dependence of the elastic intensity under the water peak maximum, the mean square displacement of water oxygens in the direction parallel to the DNA axis has been deduced. It varies from 0.110 Å2 at 275 K up to 0.345 Å2 at 310 K. The thermal diffuse scattering intensity is also peaked at the same Q value of the elastic intensity, indicating the presence of coherent vibrational excitations propagating along the ordered water filaments. © 1993 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 74
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An extensive and systematic search strategy to determine the conformational profile of 12 cyclic disulfide-bridged opioid peptides with varying affinities at the δ receptor has been carried out to identify the structure that is recognized by the δ receptor for each analogue. The methods and procedures used here for the conformational search have already been validated for [D-Pen2, D-Pen5] enkephalin (DPDPE), one member of this family. Use of these methods led to a low-energy solution conformation of DPDPE in excellent agreement with all the geometric properties deduced from its solution nmr spectra. Each of the analogue was subjected to the same procedure, involving a combination of molecular dynamics simulations at high and low temperature. The study was repeated in two environmental conditions, an apolar environment, simulated by using a distance-dependent dielectric constant, and a polar environment by embedding the peptides in a high constant dielectric ( ε = 80). An automated comparison of the different conformers based on their backbone rms and average distance between the key aromatic moieties was followed by graphic analysis using maximum structural overlap. The cross-comparison of the conformations for each analogue revealed a unique conformer that may be recognized by the δ receptor for each high-affinity analogue that permitted maintaining the critical elements required for recognition in a simple spatial orientation, while maximizing similarity in other regions. © 1993 John Wiley & Sons, Inc.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 75
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 33 (1993), S. 723-723 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 76
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 33 (1993), S. 725-733 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Zwitterionic L-alanine forms crystals containing strong hydrogen-bonding and methyl-methyl interactions. Well-defined low-frequency lattice vibrations exist in the crystals involving correlated intermolecular motions on the picosecond timescale. A characterization of these vibrations is expected to provide useful information on the nature of nonbonded interactions in peptides and proteins. We examine some of the vibrations using coherent inelastic neutron scattering and computer simulation techniques. The neutron scattering measurements are used to determine phonon dispersion relations for the acoustic and some low-frequency optic modes in the crystal. There is evidence for interaction between the two lowest frequency optical phonons and the longitudinal acoustic mode. The velocity of sound is anisotropic and can be correlated with the hydrogen-bonding arrangement in the crystal. Corresponding phonon dispersion relations are derived from normal mode analyses of the crystal using the program CHARMM. Although some calculated vibrational frequencies are somewhat too high, the form of the calculated dispersion relations are in good agreement with experiment. © 1993 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 77
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The conformation of two agonist-antagonist pairs of bradykinin (Arg1-Pro2-Pro3-Gly4-Phe5-Ser6-Pro7-Phe8-Arg9) analogues were studied in CD3OH/H2O solution by 1H-nmr techniques. The first agonist peptide studied, D-Arg0-Arg1-Pro2-Hyp3-Gly4-Thi5-Ser6-Pro7-Thi8-Arg9, differs from the bradykinin sequence by the addition of D-Arg0, the replacement of the Phe moieties in positions 5 and 8 by Thi (Thi = β-(2-thienyl)-L-alanine), and Hyp3 (Hyp = L-4-hydroxy-L-proline) in position 3. In the corresponding antagonist sequence, Pro7 is replaced by D-Phe7. The second agonist-antagonist pair studied does not contain the D-Arg0 residue, which is present only to slow down the rate of metabolism. Based on complete resonance assignments from two-dimensional total correlation spectroscopy and rotating frame nuclear Overhauser effect spectroscopy spectra at 500 MHz, the peptides were analyzed in terms of intraresidue, sequential, and medium-range nuclear Overhauser effects, amide proton temperature coefficients, and vicinal coupling constants. Both agonist peptides show clear evidence for the existence of a type I β-turn comprising the C-terminal residues Ser6-Pro7-Thi8-Arg9 in fast conformational equilibrium with extended structures throughout. Although the conformational space is dominated by extended structures, the presence of the β-turn is spectroscopically clearly discernible. The two antagonist peptides, on the other hand, do not show evidence of turn formation but rather the presence of an extended conformation with some irregularities in the N-terminal region of the peptide. While the existence of a turn at the C-terminal end of bradykinin and its analogues with agonist activity has been predicted by empirical calculations and measurements in very apolar solvents, this study, for the first time, provides evidence based on physical data in a polar solvent environment that the turn is present, that it is type I and that it is essential for agonist activity. In the particular solvent used in these studies, the Pro7 to D-Phe7 substitution precluded the formation of the turn for the C-terminal residues of the antagonist. © 1993 John Wiley & Sons, Inc.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 78
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 33 (1993), S. 1001-1001 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 79
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 33 (1993), S. 1003-1017 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In this article a few methods or modifications proven to be useful in the conformational examination of peptides and related molecules by molecular dynamics are illustrated. The first is the explicit use of organic solvents in the simulations. For many cases such solvents are appropriate since the nmr measurements (or other experimental observations) were carried out in the same solvent. Here, the use of dimethylsulfoxide and chloroform in molecular dynamics is described, with some advantages of the use of these solvents highlighted.A constant allowing for the scaling of the nonbonded interactions of the force field, an idea previously employed in distance geometry and simulated annealing, has been implemented. The usefulness of this method is that when the nonbonded term is turned to zero, atoms can pass through each other, while the connectivity of the molecule is maintained. It will be shown that such simulations, if a sufficient driving force is present (i.e., nuclear Overhauser effects restraints), can produce the correct stereoconfiguration (i.e., chiral center) as well as configurational isomer (i.e., cis/trans isomers).Lastly, a penalty term for coupling constants directly related to the Karplus curve has been plemented into the potential energy force field. The advantages of this method over the commonly used dihedral angle restraining are discussed. In particular, it is shown that with more than one coupling constant about a dihedral angle a great reduction of the allowed conformational space is obtained. © 1993 John Wiley & Sons, Inc.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 80
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Using a sensitive birefringence instrument, the birefringence arising from the orientation of the DNA chain during electrophoretic transport has been recorded. This birefringence is shown to proceed both from the alignment (stretching) of the molecule in the direction of the electric field and from the extension of the length of its primitive path (overstretching). The contribution of these two processes can be separated in the decay of the birefringence after the end of the application of the electric field. The fast relaxation of the overstretching occurs first and is demonstrated to be the main contribution to the birefringence. The orientation factor of the remaining stretched state and its decay can be quantitatively understood using the biased reptation model. It provides, in addition, a high value for the tube diameter or gel pore size a (4500 ± 450 Å for a 0.7% agarose gel with a c-0.6g dependence in the agarose concentration cg) and a low value for the effective charge per base pair (0.2e as compared to 0.5e using the condensation hypothesis). The contribution of overstretching to the birefringence is also quantitatively interpreted in term of the change in the mean length l of DNA inside a pore size a. The dynamics of decay of this overstretching is well represented by a stretched exponential with a stretching exponent α = 0.44. The mean decay time decreases slightly with increasing fields and scales with the overall DNA length close to N20. © 1993 John Wiley & Sons, Inc.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 81
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The cyclic tetrapeptide cyclo(-Pro1-Ala2-D-Phe3-Leu4-) was modeled and synthesized to be used for molecular interactions and chiral discrimination studies in CDCl3. Total correlation spectroscopy and nuclear Overhauser effect spectroscopy spectra of the cyclic tetrapeptide showed the presence of one dominant stereoisomer - 1 - and three minor ones -  2a, 2b, and 2c - in a relationship of 92:6:1:1. They formed three- to five-hydrogen bond complexes with Boc-D-Ser, Boc-L-Ser and Boc-L-Thr (Boc: t-butyloxylcarbonyl). These three Boc-amino acids interact more strongly with 2a, 2b, and 2c than with 1, altering their relative concentrations to 48:40:6:6. In the complex between the cyclic tetrapeptide and Boc-D-Ser, the stereoisomer 2a exchanged chemically with 1, 2b, and 2c, while 1 did not exchange with either 2b or 2c. This chemical exchange is due to cis-trans isomerization of the peptide bonds. The chiral discrimination of 2a, 2b, and 2c was stronger than that of 1. No complexation occurred with Boc-L-Ala or Boc-L-Trp. © 1993 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 82
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 33 (1993), S. 1423-1429 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: We analyze the implications of various choices for atomic friction coefficients on a recent theory of long-time peptide dynamics. One method for determining atomic friction coefficients is based on calculating effective hydrodynamic radii from the reduction of the atomic surface area accessible to solvent, while another employs an additive van der Waals radii model. These friction coefficients are used to evaluate the orientational correlation times of bonds in the peptide fragment ACTH(5-10), which contains a single tryptophan probe. Three models are considered; they choose as relevant slow variables (a) the positions of the α-carbons, (b) the positions of all backbone bonds, and (c) both positions in (b) and those along side chains. Comparisons are made between the three models and with experiment. While general variations are similar, large shifts in local correlation times emerge from using the different methods. The results indicate that the extra backbone bonds do not contribute much to the memory function for the virtual bond model, but the side-chain groups have a strong effect. © 1993 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 83
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The type II and type III collagen α-1 chain N-telopeptides are a nonadecamer with the sequence pEMAGGFDEKAGGAQLGVMQ-NH2 and a tetradecamer with the sequence pEYEAYDVKSGVAGG-NH2, respectively. Their conformations have been studied in CD3OH/H2O (60/40) solution by means of two-dimensional proton nmr spectroscopy. Based on double quantum filtered correlation spectroscopy, total correlation spectroscopy, rotating frame nuclear Overhauser enhancement (ROE) spectroscopy, and nuclear Over-hauser enhancement (NOE) spectroscopy experiments, all resonances were assigned and the conformational properties were analyzed in terms of vicinal NH-Hα coupling constants, sequential and medium-range NOEs (ROEs), and amide proton temperature coefficients. The NOE distance constraints as well as dihedral constraints based on the vicinal NH-Hα coupling constants were used as input parameters for restrained molecular mechanics, consisting of restrained molecular dynamics and restrained energy minimization calculations. The type II N-telopeptide's conformation is dominated by a fused βγ-turn between Phe6 and Ala10, stabilized by three hydrogen bonds and a salt bridge between the side-chain end groups of Glu8 and Lys9. The first 5 amino acids are extended with a much higher degree of conformational freedom. The 2 Gly residues following the turns were found to be highly flexible (hinge-like), leaving the spatial position of the second half of the molecule relative to the fused βγ-turn undefined. In the type III telopeptide, a series of sequential NH(i)-NH(i + 1) ROEs were observed between the amino acids Tyr2 and Ser9, indicating that a fraction of the conformational space is helical. However, the absence of medium-range ROEs and the lack of regularity of the effects associated with α-helices suggest the presence of a nascent rather than a complete helix. © 1993 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 84
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The program AMBER 3.0 has been used to generate molecular dynamics trajectories of a poly (dA)·poly (dT) decamer. The simulations were performed using different methods to treat solvent effects. Results of a simulation including 18 counterions NH+4 and 4109 water molecules under (N, P, T) conditions were compared to simulation runs with implicit solvent representation in which solvent screening effects were represented by the use of a sigmoidal distance-dependent dielectric function. In the latter case, the system was simulated under microcanonical (N, V, E) and canonical (N, V, T) conditions. For the fully hydrated system simulation, a preequilibration protocol was developed since it was observed that long and progressive periods of heating and equilibration on the overall system were necessary in order to avoid energetic collisions between the solute and the solvent molecules, leading to severe irreversible deformation of the solute. A detailed analysis of DNA conformations, sugar puckers, and stability of the hydrogen bonds, Watson-Crick and three-center H bonds, is reported. The results show that DNA remains essentially in the B conformer with a tendency in the hydrated model to adopt a slightly distorted, unwound, and stretched conformation in comparison to standard B-DNA. Concerning sugar puckers, the mean pseudorotation phases of the adenine residues are systematically higher than those of the thymine residues, except in the case of the hydrated model for which a particular behavior is observed for the adenine strand. In this case, the terminal bases oscillate between C2′,-endo and O4′,-endo and the central ones stay in the C3′,-endo domain. The mean lifetimes of the internal Watson-Crick H-bond (A)HN6-O4(T) are also dependent on the base pairs included in the calculation, excepted for the implicit solvent simulation at constant temperature. The three-center H bonds have very small mean lifetimes in all three cases of MD simulation. In the minor groove of the hydrated model, a spine of hydration is found as observed by x-ray crystallography and other theoretical simulations. On the basis of the rms deviations, it appears that the fully hydrated simulation has not reached a plateau at the end of the run, while the implicit simulation at constant energy seems to have converged. At constant temperature, very large oscillations in rms deviations are observed. © 1993 John Wiley & Sons, Inc.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 85
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 33 (1993), S. 1591-1603 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The energetics of the χ12χ3χ22 portion of the disulfide bridge have been obtained from an ab initio study of diethyl disulfide. Calculations at the 3-21G* level were done on relaxed structures at every ∼ 30° in χ12 and χ22, and the additional energies for small Δχ3 were obtained. Complete E(χ12, χ22) and χ03(χ12, χ22) maps were computed from Fourier series expansions. These results have been used to calculate the energetics of 92 disulfide bridges in known protein structures, and to compare ab initio and molecular mechanics energies for some observed and predicted bridges. The differences found in relative energies and in χ03 values suggest that present energy functions give a limited description of the structural and energetic properties of the disulfide bridge. © 1993 John Wiley & Sons, Inc.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 86
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 33 (1993), S. 1605-1616 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Based on Lifson-Roig's helix-coil transition theory, substitution of a single heteroresidue into a homopolymer host is studied. This study models recent experiments that substitute a single amino acid into a small peptide in water [A. Chakrabartty, J. A. Schellman, and R. L. Baldwin (1991), Nature, Vol. 351, pp. 586-688]. Our formalism, which is based on a perturbation method, differs from the existing theory for sequenced polymers and is naturally analogous, hence likely to be useful, to substitution experiments in the laboratory. It is shown that the intrinsic helix propensity w is directly proportional to the equilibrium constant for the helix-coil equilibrium of a single residue in a host peptide. This intuitive new result will simplify experimental data interpretations for measurements of the helical conformation on the single amino acid level. It is also shown that substitution affects the total helicity of the host peptide according to two considerations: the helicity of the replaced residue prior to the substitution, and the sensitivity of the site, a measure of neighboring interactions. The relationship between substitution stability and thermal stability is explored. © 1993 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 87
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The molecular and crystal structures of one derivative and three homopeptides (from the di-to the tetrapeptide level) of the chiral, Cα, α-disubstituted glycine Cα-methyl, Cα-benzylglycine [(αMe)Phe], have been determined by x-ray diffraction. The derivative is mClAc-D-(αMe)Phe-OH, and the peptides are pBrBz-[D-(αMe)Phe]2-NHMe, pBrBz-[D-(αMe)Phe]3-OH hemihydrate, and pBrBz-[D-(αMe)Phe]4-OtBu sesquihydrate. All (αMe)Phe residues prefer φ,ψ torsion angles in the helical region of the conformational map. The dipeptide methylamide and the tripeptide carboxylic acid adopt a β-turn conformation with a 1 ← 4 C=O…H—N intramolecular H bond. The structure of the tripeptide carboxylic acid is further stabilized by a 1 ← 4 C=O…H—O intramolecular H bond, forming an “oxy-analogue” of a β-turn. The tetrapeptide ester is folded in a regular (incipient) 310-helix. In general, the relationship between (αMe)Phe chirality and helix screw sense is opposite to that exhibited by protein amino acids. A comparison is made with the conclusions extracted from published work on homopeptides from other Cα-methylated α-amino acids. © 1993 John Wiley & Sons, Inc.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 88
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The aggregation properties of zinc-free insulin have been studied using static and dynamic light scattering. The aggregation has been investigated as a function of three parameters, the concentration of sodium chloride (in the range 10-100 mM), the pH value (in the range pH 7.5-10.5), and the insulin concentration (1.8-13.4 mg/mL). The measured homodyne autocorrelation function was used to determine the apparent mean hydrodynamic diameter as well as the apparent weight-averaged molar mass of the insulin species in solution. A method of data analysis was employed, which allows the separation of light scattering contributions from the insulin oligomers and from irrelevant macromolecules and possible impurities present in the sample solutions. Also, a simple phenomenological equilibrium model describing the association of oligomers of insulin is presented. One aspect of this model is that it makes it possible to determine weight average molar masses corrected for virial effects on the Rayleigh ratio. This was necessary because virial effects cannot be isolated and corrected for by dilution since this would change the equilibrium distribution of oligomers. The basis of the model is a positive contribution to Gibbs free energy from charge repulsion depending on the protein charge and the number of monomers in the oligomers, and an assumed constant negative contribution to Gibbs free energy arising from either an entropic gain or hydrogen bonding upon association. The equilibrium model gives a good description of both the apparent weight average molar masses and the apparent hydrodynamic diameters, when the effect of the insulin concentration is taken into account by including virial effects arising from charge-charge repulsion (Donnan effect). The result shows that the association of insulin as a function of pH and ionic strength can be described by an effective charge equal to the charge derived from proton titration reduced by the number of sodium ions binding to insulin. At the lowest pH and highest salt concentration (pH 7.5, 100 mM NaCl, 12 mg/mL insulin), the weight average molar mass is close to that of the hexamer, and at the highest pH and lowest salt concentration (pH 10.5, 10 mM NaCl, 1.9 mg/mL), the weight average molar mass is close to that of the monomer. In all cases, however, a distribution of oligomers is present with a relative Gaussian width of about 30%. Neglecting the positive term in Gibbs free energy, an upper bound to the association constant for insulin can be calculated: The negative term in Gibbs free energy corresponds to an association constant of (0.8 ± 0.3)·105M-1, which is in agreement with published values for the monomer-to-monomer association. The satisfactory agreement between theory and experiments for the weight average molar mass suggests that it should be possible to predict the aggregational properties of mutant forms of insulin. © 1993 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 89
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 13C proton-decoupled cross-polarization magic-angle spinning nmr spectra of bovine serum albumin are reported as a function of hydration. Increases in hydration level enhance the resolution of the peak centered at about 40 ppm but has little or no effect on the other spectral peaks. Hydration has little effect on either the rotating frame proton spin-lattice relaxation time or the cross-relaxation time for any of the peaks, suggesting that the efficiency of dipolar coupling is largely preserved on hydration of the protein. Resolution enhancement of the peak at 40 ppm is not understood, but possible sources of the behavior include a decrease in the line width of contributing resonances from lysine ε carbons due to increased motional averaging on hydration, reordering of disulfide bridges, and titration shifts induced by hydration. Hydration of bovine serum albumin appears to have little effect on the distribution of conformations sampled by the protein so that the broad distribution of conformations observed in the dry state is also observed in the fully hydrated state. This is in contrast to lysozyme where significant ordering of the conformation is seen on hydration. © 1993 John Wiley & Sons, Inc.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 90
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 33 (1993), S. 1901-1908 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: High-resolution proton spectra at 500 MHz of two tachykinin peptides, substance P methyl ester (SPOMe) and [Nle10]-neurokinin A (4-10), have been obtained in dimethylsulfoxide (DMSO), and for SPOMe, also in 2, 2, 2-trifluoroethanol (TFE)/water mixtures. Complete chemical shift assignments for these peptides were made based on two-dimensional (2D) nmr techniques, correlated spectroscopy and total COSY. J coupling measurement and nuclear Overhauser effect spectroscopy (NOESY) were then used to determine the conformation of these peptides in the various solvents. Based on the J coupling, NOE correlations, and temperature coefficients of the NH resonances, it is concluded that these two peptides exist in DMSO at room temperature as a mixture of conformers that are primarily extended. For SPOMe in TFE/water with high TFE content, however, helical structures are found to be present, and they become quite clear at temperatures between 270 and 280 K. The variation of the 13C chemical shifts of the Cα (the secondary shift) with TFE contents corroborates this conclusion. The NOE and Cα shifts show that the main helical region for SPOMe lies between 4P and 9G. The C-terminus segment L—M—NH2 is found to be quite flexible, which appears to be quite common for neurokinin-1 selective peptides. © 1993 John Wiley & Sons, Inc.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 91
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The peptides Ac-ΔPhe-Ala-ΔPhe-NH—Me (1), Ac-ΔPhe-Val-ΔPhe-NH—Me (2), Ac-ΔPhe-Gly-ΔPhe-Ala-OMe (3), and Boc-Ala-ΔtPhe-Gly-ΔPhe-Ala-OMe (4), containing two dehydro-phenylalanine (ΔPhe) residues, were synthesized and the solution structure investigated in various solvents. The nmr and CD measurements indicate that all the dehydropeptides examined adopt 310-helical conformations in solution. The tripeptides 1 and 2 exibited an intense negative CD exciton couplet, which was assigned to the right-handed screw sense, while the tetrapeptide 3 displayed a CD couplet having opposite sign, which was assigned to the left-handed helical sense. In the pentapeptide 4 the sense of the helix was found to vary with solvent and temperature, as demonstrated by the sign reversal of the CD spectrum. The right-handed sense dominates in hexafluoro-2-propanol, whereas a left-handed helix prevails in chloroform, acetonitrile and methanol. A crucial role for this behavior is likely to be played by the two alanine residues positioned respectively at the head and tail of the sequence, which favor conformations having opposite screw senses. © 1993 John Wiley & Sons, Inc.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 92
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 33 (1993), S. 37-44 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The influence of sugar ring flexibility in DNA on the mechanism of the B ⇄ A conformational transition is studied. The dipole moment of the deoxyribose as a function of its puckered states is calculated by the quantum-mechanical method using the MINDO/3 approximation. The interaction of the sugar dipole with the neighbor molecular groups in polynucleotide chains is estimated. The sugar dipole interaction with phosphate groups and counterions is shown to be strong and capable to deform the pseudorotation potential of deoxyribose. The effective pseudorotation potential of sugar ring in the B and A helices is obtained. The results are used to explain the behavior of Raman bands in the region of sugar-phosphate vibrations. The mechanism of the effect of electrostatic forces on the sugar-phosphate backbone conformation, which is essential for the B ⇄ A and other structure transitions, is offered. © 1993 John Wiley & Sons, Inc.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 93
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 33 (1993), S. 107-115 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Assignment of the hydrogen spectrum is the first step in the conventional procedure for the determination of molecular structure by 1H-nmr. In this paper, we explore the possibility of directly exploiting the distances derived from nuclear Overhauser effect experiments to generate a three-dimensional structure that is then assigned based on knowledge of the connectivity or primary sequence. This effort is analogous to that of the protein crystallographers in tracing electron density of the peptide chain. In particular, we compare structures produced by distance geometry to known peptide secondary structures to see what level of information is required to “trace” the backbone α-carbon and amide hydrogens and the β-carbon hydrogens. We conclude that this approach is only useful with excellent quality stereo-resolved data. © 1993 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 94
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of the hydrodynamic volume change associated with the unfolding and refolding of a globular protein can be observed using high performance size exclusion chromatography. Chromatographic profiles that evidence such dynamics can be simulated using equations in which Chromatographic partitioning and the conformational transition are described in terms of a finite difference algorithm incorporating an apparent binding model to generate broad and asymmetric peaks. Application of these equations to the simple two-state unfolding transition of ribonuclease A in guanidine hydrochloride indicates that reliable kinetic parameters can be obtained using these equations. © 1993 John Wiley & Sons, Inc.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 95
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 96
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Dynamic light scattering measurements were performed on dilute aqueous solutions of native ovalbumin (OA) and on those of linear OA aggregates induced by thermal denaturation at low ionic strength and neutral pH. The weight-average molecular weight Mw of four aggregates tested ranged from 1,700,000 to 5,500,000. The translational diffusion coefficient D0 of native OA at infinite dilution was estimated as 8.70 × 10 -7 cm2/s, which gave 56.0 Å as the diameter of the rigid spherical particle. The intensity autocorrelation function of linear OA polymers was analyzed with the cumulant method to obtain the first cumulant Λe. The dependence of Λe on the scattering vector q at very low polymer concentration was found intermediate between those of a flexible chain and a rigid rod. The translational diffusion coefficient Dtr [≡ (Te/q2)q → 0] was in proportion to Mw-0.55, and the magnitude was in good agreement with a value calculated from the wormlike cylinder model with values of three parameters determined in an earlier study, ML = 1600 Å-1, d = 120 Å, and Q = 230 Å, where ML, d, and Q are the molecular weight per unit length, diameter, and persistence length, respectively. Based on these results, a new model, to be called as the dimer model, was proposed to interpret the formation mechanism of linear OA polymers induced by thermal denaturation. © 1993 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 97
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 98
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 210 (1993), S. 173-196 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Durch radikalische Kettenübertragung ausgelöste Pfropfcopolymerisationen von Polyestern rnit Styrol wurden untersucht. Als Rückgratkette diente ein Modellpolyester aus trans- 1,4-Cyclohexandiol und Sebacinsäuredichlorid. Ferner wurden flüssigkristalline Polyester rnit 1,4 : 3,6-Dianhydrosorbit und 1,4-Anhydroerythrit als Diolkomponenten hergestellt und zur Pfropfcopolymerisation mit Styrol eingesetzt. Polymerblends aus Tetramethylbisphenol A-Polycarbonat und den ungepfropften sowie mit Styrol gepfropften flüssigkristallinen Polyestern wurden durch gemeinsame Fällung von Polymerlösungen erhalten; ihr Verhalten wurde mit Torsionspendelmessungen, dynamisch-mechanischer Thermoanalyse und Elektronenmikroskopie untersucht. Der gepfropfte Polyester erwies sich dabei als wirksamer Phasenvermittler.
    Notes: Graft copolymerizations of polyesters with styrene by free-radical chain transfer reactions were investigated. A model polyester of trans-l,4-cyclohexanediol and sebacoy1 dichloride was used as backbone chain. The graft products were characterized. Furthermore, liquid crystalline polyesters with 1,4 : 3,6-dianhydrosorbitol and 1,4-anhydroerythritol as diol components were synthesized and used in graft copolymerizations with styrene. Polymer blends of tetramethylbisphenol A polycarbonate and the LC-polyester with and without polystyrene grafts were prepared by common precipitation of polymer solutions and their behaviour was examined by torsion pendulum, dynamic-mechanical thermoanalysis and scanning electron microscopy. The grafted polyester turned out to be an efficient phase compatibilizer.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 99
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 211 (1993), S. 9-19 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Neue synthetische, unvernetzte Anionenaustauscher-Membranen wurden aus Lösungen von quanternisierten Chlormethylstyrol-Methylmethacrylat-Copolymeren mit 64.0, 42.9, 19.7, 12.9 und 11.0 mol-% Chlormethylstyrol hergestellt.Ionenaustauschkapazität, Wasseraufnahme und physikochemische Eigenschaften (Membranpotential und Überführungszahlen) der Membranen wurden ermittelt. Die Membranen können nach Behandlung der Copolymeren mit tertiären Aminen hergestellt werden, wobei die Membranen aus Copolymeren mit 12, 9 bzw. 11,0 mol-% Chlormethylstyrol eine ausgezeichnete Dimensionsstabilität und mechanische Festigkeit gegen verdünnte Säuren, verdünnte Laugen und Salzlösungen besitzen und in einer Reihe organischer Lösemittel wie Aceton, Methylethylketon und Methanol löslich sind. Ihre Anionen-Überführungszahlen in 0,01 N und 0,03 N KC1-Lösungen betrugen 0,96 bzw. 0,97, ermittelt aus Membranpotentialmessungen.
    Notes: New synthetic noncross-linked anion exchange membranes have been prepared by casting a solution of quaternized chloromethylstyrene-methyl methacrylate copolymers containing 64.0, 42.9, 19.7, 12.9 and 11.0 mol-% chloromethylstyrene. The ion exchange capacity, water content and physicochemical properties (membrane potential and transport number) of these membranes were studied. The results showed that the copolymers can be fabricated in membrane form after treatment with tertiary amine, of which the membranes produced from the 12.9 and 11.0 mol-% copolymer exhibited excellent dimensional stability and mechanical strength towards dilute alkali solution, dilute acid solution and salt solution, and were soluble in a variety of organic solvents, such as acetone, methyl ethyl ketone and methanol. Their anion transport numbers determined from the membrane potential measurements in 0.01 N and 0.3 N KCI solution were 0.96 and 0.97, respectively.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 100
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 211 (1993), S. 21-34 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: (Polystyrol-block-polyisopren-block-polystyrol)-graft-poly(1-vinylimidazol) (SISg-VIm) wurde durch strahlungsinduzierte Pfropfcopolymerisatio von1-Vinylimidazol auf (Polystyrol-block-polyisopren-block-polystyrol)hergestellt und mit kobalthaltigen Schiffschen Basen (CoS) komplexiert. Aus Lösungen dieser Produkte wurden Memberanen hergestellt und untersucht. Die Koordinationszahlen und Gleichgewichtskonstanten der Komplexbildungsreaktionen sowie die thermodynamischen Parameter der Sauerstoffadorption und -desorption der Membranen wurden durch UV-VisSpektroskopie ermittelt. Die Sauerstoffdurchlässigkeiten und O2/N2-Permselektivitäten der Membranen wurden bei verschiedenen Gegenstrom-Gasdrücken und Temperaturen gemessen. Die erhöhte Sauerstoffdurchlässigkeit kann durch eine dual-modeTheorie beschrieben werden.
    Notes: Membranes of (polystyrene-block-polyisoprene-block-polystyrene)-graft-poly(1-vinyl-imidazole) (SIS-g-VIm) reacted with three cobalt-containing Schiff bases (CoS) were prepared and studied. SIS-g-VIm was obtained by radiation-induced graft copolymerization of 1-vinylimidazole onto poly(styrene-block-isoprene-block-styrene) triblock copolymer. Membranes of SIS-g-VIm reacted with three cobalt-containing Schiff bases (SIS-g-VIm-CoS) were prepared by the solution casting method. The co-ordination numbers and formation constants of these reactions were determined. Equilibrium constants and thermodynamic parameters of SIS-g-VIm-CoS membranes for binding and dissociation of oxygen were determined by UV/VIS spectroscopy. The permeability and O2/N2 permselectivity of the SIS-g-VIM-CoS membranes were measured at various upstream gas pressures and temperatures. Oxygen permeation through the SIS-g-VIm-CoS membranes can be explained by dual-mode-facilitated transport theory.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...