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  • Articles: DFG German National Licenses  (3,890)
  • 1985-1989  (3,890)
  • 1955-1959
  • 1945-1949
  • 1988  (3,890)
  • Polymer and Materials Science  (3,199)
  • Chemical Engineering  (691)
Source
  • Articles: DFG German National Licenses  (3,890)
Material
Years
  • 1985-1989  (3,890)
  • 1955-1959
  • 1945-1949
Year
  • 101
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 157 (1988), S. 177-187 
    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 alkalischen Hydrolyse von Glimmer-Acrylnitril-Pfropfcopolymeren wurde untersucht. Die Abhängigkeit des Verseifungsgrades von der Alkalikonzentration und der Hydrolysezeit wurde bestimmt. Chemische und spektroskopische Techniken wurden zur Bestimmung des Hydrolysemechanismus herangezogen.
    Notes: Kinetics of alkaline hydrolysis of mica-acrylonitrile graft copolymers was studied. The dependence of alkali concentration and the time of hydrolysis on the degree of saponification was determined. Chemical and spectroscopical techniques were used to determine the mechanism of hydrolysis.
    Additional Material: 4 Ill.
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  • 102
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 157 (1988), S. 153-163 
    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 Behandeln von Baumwollgewebe mit Schwefelkohlenstoff in Gegenwart von NaOH ergibt Cellulosethiocarbonat, welches mit Cerammoniumnitrat (CAN) einen Komplex bildt. Nach ausgiebigem Waschen war das CeIV-Cellulosethiocarbonat fähig, die vinylische Pfropfpolymerisation auf Baumwollgewebe ohne Homopolymerbildung zu initiieren. Die Pfropfausbeute wuchs im Falle von Methylmethacrylat mit wachsenden CAN-Gehalt (0 - 50 mmol/l) und steigender Temperatur (60 - 80°C). Bei pH 2 war die Pfropfung besonders begünstigt. Dagegen wurde die Pfropfung im alkalischen Bereich gestoppt. Die Zugabe von bis zu 7% Methanol, Ethanol oder Isopropanol zum wäßrigen Polymerisationsmedium erhöhte die Pfropfausbeute bedeutend; hierbei wurde mit Isopropanol die hdchste Steigerung erhalten. Hdhere Alkoholmengen dagegen erniedrigten die Ausbeute. Die Pfropfgeschwindigkeit ist anfangs hoch, spater wird die Pfropfungsreaktion langsamer. Unabhingig von den verwendeten Reaktionsbedingungen war eine Reaktionszeit von 60 Minuten ausreichend. Es wurde die Fahigkeit des Cdv-Cellulosethiocarbonats untersucht, die Pfropfung mit Methylmethacrylat, Acrylnitril und Acrylamid zu initiieren. Dabei ergab sich fur die Pfropfgeschwindigkeit folgende Reihenfolge: Methylmethacrylat 〉 Acrylnitril 〉 Acr ylamid.
    Notes: Treatment of cotton fabric with carbon disulphide in presence of NaOH resulted in cellulose thiocarbonate. The latter formed a complex when treated with ceric ammonium nitrate (CAN). After being thoroughly washed, the CeIV cellulose thiocarbonate was capable of initiating vinyl graft polymerization onto cotton fabric without homopolymer formation. The graft yield obtained with methyl methacrylate was found to increase by increasing CAN from zero to 50 mmol/l at temperatures from 60 to 80°C. Grafting was greatly favoured at pH 2; alkaline pH offset grafting. Incorporation of up to 7% of methanol, ethanol, or isopropanol in the aqueous polymerization medium enhanced grafting significantly with the certainty that the highest graft yield was obtained with isopropanol; using higher alcohol percentages decreased grafting. The rate of grafting showed an initial fast rate followed by a slower rate; 60 minutes reaction time proved appropriate for grafting irrespective of the condition used. In addition to methyl methacrylate the ability of CeIV-cellulose thiocarbonate to induce grafting of acrylonitrile and acrylamide was also examined. The rate of grafting followed the order methyl methacrylate 〉 acrylonitrile 〉 acrylamide.
    Additional Material: 5 Ill.
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  • 103
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 157 (1988), S. 165-176 
    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: Aus der Röntgenkleinwinkelstreuung von aus der orientierten Schmelze kristallisierten Legierungen aus isotaktischem Polypropylen und Poly(1-buten) wurden Grenzflächenverteilungsfunktionen berechnet. Die Proben enthalten Nadelkristalle, die in Bezug auf ihre Abstandsverteilung ein „verdünntes System“ darstellen. Es wird gezeigt, daß die Berechnung von Grenzflächenverteilungsfunktionen aus jeweils nur zwei Grenzflächen möglich ist. Der Vergleich der erhaltenen Nadeldicken mit Ergebnissen aus anderen Auswertemethoden ergibt eine gute Übereinstimmung.
    Notes: Interface distribution functions have been evaluated from the equatorial small angle x-ray scattering of blends of isotactic polypropylene and poly(1-butene) crystallized in the shear field of the oriented melt. The samples contain core fibrils which represent a diluted system with respect to their distance statistics. It is shown, that interface distribution functions can be calculated from only two interfaces (diffuse phase boundaries between fibrils and amourphous phase). The calculated thicknesses agree well with values determined from other methods.
    Additional Material: 8 Ill.
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  • 104
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 157 (1988), S. 199-199 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: No Abrstract.
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  • 105
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: This paper accumulates the mechanism and kinetics of oxidation and the inhibition mechanism of oxidation processes using preventive antioxidants, chain-breaking antioxidants and deviations from the simple inhibition mechanism.
    Additional Material: 4 Ill.
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  • 106
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 160 (1988), S. 83-90 
    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 Poly(methylvinylketon) und acetyliertem Polystyrol mit Phenol in Gegenwart von HCl oder H2SO4 wurde untersucht, um Polymere mit Strukturen ähnlich dem Bisphenol A zu erhalten. Die Reaktion an Poly(methylvinylketon) führt zu intramolekularer Aldol-Kondensation, während acetyliertes Polystyrol die gewünschte Bisphenol A-Struktur liefert.
    Notes: The reaction of polymers containing carbonyl groups such as poly(methyl vinylketone), poly(methyl vinyl ketone-co-styrene) and acetylated polystyrene with phenol in the presence of HCI or H2SO4 has been studied in order to produce bisphenol A type structure on the polymer chain. Poly(methyl vinyl ketone) shows intramolecular aldol condensation and acetylated polystyrene results in bisphenol A type structure.
    Additional Material: 4 Ill.
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  • 107
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 160 (1988), S. 29-39 
    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: In der vorliegenden Arbeit wird der Einfluß der Verformungsamplitude, der Temperatur und der Frequenz auf die dynamischen Eigenschaften von SBR-Faserverbundstoffen untersucht. Der Einbau von Kurzfasern erhöht den Speichermodul bei beliebiger Verformungsamplitude. Je nach Fasertyp verringert sich die lineare Reaktionszone des Moduls auf die Verformung oder verschwindet vollkommen. Der Verlustfaktor tan δ ist größer bei Faserverbundstoffen, obwol die Signale größenmäßig sich nicht verändern, lediglich die entsprechende Verformung.Bei Temperaturanstieg verringert sich der Modulwert, jedoch ist dieser Abfall weniger stark ausgeprägt im Faser-SBR-Verbund. Die Relaxationsspektren zeigen eine maximale Dämpfung, die der Hauptrelaxation in der Elastomermatrix entspricht. Die Temperatur,bei der dieses Maximum auftritt, verlagert sich zu höheren Werten mitsteigender Anregungsfrequenz. Dadurch wird die Ermittlung der scheinbaren Relaxationsaktivierungsenergie möglich, die im Verbund Faser-Haftmittel-SBR höher ist (225-275 kJ/mol) als in dem faserfreien Stoff (194.6 kJ/mol) als Folge einer stärkeren Faser-Matrix-Wechselwirkung.
    Notes: This paper examines the effects of deformation amplitude, temperature and frequency on the dynamic properties of SBR-short fiber composites. The presence of the fiber increases the storage modulus at any deformation amplitude. Depending on the nature of the fiber, the linear response zone of the modulus versus deformation either diminishes or disappears. The loss factor tan δ is higher in fiber composites. Although the peaks do not vary in magnitude, they occur at different deformation amplitudes.Temperature increase causes the moduli to decrease, the gradient, however, being less pronounced for fiber composites. The relaxation spectra show a damping peak which correlates to the principal relaxation process in the elastomeric matrix. The temperature at which this peak appears is displaced towards higher values with increasing excitation frequency. This allows the determination of the apparent relaxation activation energy, which is higher in fiber plus adhesive composites (225 - 275 kJ/mol), as compared to the fiber-free composite (194 kJ/mol), as a consequence of stronger fiber-matrix interaction.
    Additional Material: 7 Ill.
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  • 108
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 160 (1988), S. 41-66 
    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 wurde ein neuer Typ eines UV-härtbaren Polyurethanacrylatharzes synthetisiert, das auf hydroxyterminierten Polydimethylsiloxan (PDMS)-Weichsegmenten mit einem Molekulargewicht von 1800 und 2,4-Toluoldiisocyanat (TDI)/2-Hydroxyethylmethacrylat (HEMA) Hartsegmenten basiert. Die Reaktivität von 2,4-TDI mit den Hydroxygruppen von Silanol und HEMA wurde anhand von IR-Messungen diskutiert. Die charakteristischen Absorptionspeaks der NCO-Gruppen von 2,4-TDI in para- und ortho-Stellung sollten mit zunehmender Reaktionszeit abnehmen.Die Meßmethodik der wesentlichen physikalischen Eigenschaften dieser Art von UV-härtbaren Materialien wurde ebenso wie auch der Einfluß verschiedener reaktiver Verdünnungsmittel und einiger Pigmente untersucht. Dieses Harz mit guten optischen, elektrischisolierenden und Hafteigenschaften an verschiedenen Matrizes konnte in den chemischen Eigenschaften verbessert und die Viskosität reduziert werden, während die Beschichtungsverarbeitbarkeit durch Mischen mit verschiedenen reaktiven Verdünnern gefördert wurde. Die hervorragenden Hafteigenschaften auf Glasplatten wurden der ähnlichen Struktur zwischen den PDMS Weichsegmenten und Glas zugeschrieben, was eine breite Anwendung in der Beschichtungsindustrie erschließt.
    Notes: A new type of a UV-curable polyurethane acrylate resin based on hydroxyterminated polydimethylsiloxane (PDMS) soft segments with molecular weight 1800 and 2,4-toluene diisocyanate (TDI)/2-hydroxyethyl methacrylate (HEMA) hard segments were synthesized. The reactivity of 2,4-TDI with the hydroxy groups of silanol and HEMA was discussed by means of IR measurements. The characteristic absorption peaks of the  - NCO groups of 2,4-TDI in the para- and ortho-position should decline with increasing the reaction time. The measurements of fundamental physical properties of this type of UV-curable materials had been widely studied in addition to the effects of using various reactive diluents and some pigments. This kind of resin with good optical, electrical insulating, and adhesive properties on various matrices, could be improved in chemical properties and reduced in viscosity while promoting the coating processability by mixing with various reactive diluents. The excellent adhesive properties on glass plates can be attributed to the similar structure between the PDMS soft segments and glass which makes the application in the coating industry possible.
    Additional Material: 18 Ill.
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  • 109
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A typical intumescent fire retardant additive for polypropylene, which is a mixture of ammonium polyphosphate and pentaerythritol, does not sensibly modify the photooxidative behaviour of unstabilized polypropylene whereas it modifies that of polypropylene stabilized with a substituted o-hydroxybenzophenone and a sterically hindered amine. The photostabilizing effectiveness of the amine is probably decreased owing to protonation by polyphosphoric acid. On the contrary, the photo-protection effectiveness of the o-hydroxybenzophenone is increased in the presence of the intumescent fire retardant. This might be due to a photoinhibition effect of pentaerythritol.
    Additional Material: 2 Ill.
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  • 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: Beginning with the current theories concerning the solid state structure of bisphenol-A-polycarbonate, the effect of chemical substitution of the bisphenol upon the thermal, mechanical, and dynamic mechanical properties will be discussed in detail. The observed mechanical properties of the various polycarbonates is considerably influenced by their chemical structure. Among all of the polycarbonates, bisphenol-A-polycarbonate is unique, particularly with respect to its low temperature properties. The ductile-to-brittle transition as a function of temperature correlates to the high temperature region of Gamma relaxation (G′′). Any theoretical approach to completely characterize and describe the experimentally observed phenomena must take into consideration as a fundamental parameter the conformational flexibility of the polycarbonate chain.
    Notes: Ausgehend von den bisher erarbeiteten Vorstellungen über die Festkörperstruktur des Bisphenol-A-Polycarbonats wird die Auswirkung einer chemischen Substitution des Bisphenols auf die thermischen, mechanischen und mechanisch-dynamischen Eigenschaften diskutiert. Innerhalb der Substanzklasse der Polycarbonate zeigt sich dabei hinsichtlich der beobachteten mechanischen Phänomene ein erheblicher Einfluß der chemischen Struktur. Vor allen Polycarbonaten ist das Bisphenol-A-Polycarbonat besonders hinsichtlich seiner Tieftemperatur-Eigenschaften ausgezeichnet. Der Spröd/Zäh-Übergang als Funktion der Temperatur korreliert mit der Hochtemperaturflanke des mechanischen Nebenrelaxationsgebietes. Eine die experimentell beobachteten Phänomene vollständig charakterisierende Theorie muß als wesentlichen Parameter die konformative Beweglichkeit der Polycarbonat-Ketten berücksichtigen.
    Additional Material: 4 Ill.
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  • 111
    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: Mischungen von Elastomeren wie Naturkautschuk und Styrol-Butadien-Kautschuk werden bei verschiedenen Temperaturen vulkanisiert und die Behandlungscharakteristika und Vulkanisateigenschaften verglichen. Die optimale Behandlungszeit bei einer bestimmten Vulkanisationstemperatur konnte empirisch durch eine Exponentialbeziehung dieser Temperatur ausgedrückt werden. Die Vernetzungsdichte der Vulkanisate nimmt mit steigender Vulkanisationstemperatur ab. Für eine vorgegebene Mischung gibt es eine bestimmte Vulkanisationstemperatur, bei der die Materialien die besten Eigenschaften für spezifische Anwendungen besitzen.
    Notes: Gum compounds of natural rubber (NR) and styrene-butadiene rubber (SBR) are vulcanized at different temperatures and the cure characteristics and vulcanizate properties are compared. The optimum cure time at a particular vulcanization temperature could be expressed empirically in terms of that temperature using an exponential relation. The crosslink density of the vulcanizates is found to decrease with an increase in the vulcanization temperature. For a given compound there is a particular vulcanization temperature which gives the best compromise of properties for specific applications.
    Additional Material: 8 Ill.
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  • 112
    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: Thermisch polymerisierte Proben von linearen Additionspolymeren des Bisphenol-A-Diglycidylethers (DGEBA) mit den drei unterschiedlichen Aminen, (A) Benzylamin (BA), p-Chloranilin (PCA) und Cyclohexylamin (CHA), wurden mittels Gelpermeationschromatographie (GPC) unter Verwendung von THF als Elutionsmittel untersucht.Bei der Eichung des Systems und der Interpretation der Chromatogramme wurde der Solvatationseffekt der Hydroxylgruppen durch THF berücksichtigt. Der Vergleich der Chromatogramme weist darauf hin, daß das Polymere mit CHA schon im Bereich kleiner Molmassen (einschließlich der Dimeren) und in einem frühen Reaktionsstadium cyclisiert. Der Vergleich der mittleren Molmassen der Proben, die nach zwei unabhiingigen Methoden  -  Dampfdruckosmometrie (VPO) und GPC  -  gemessen wurden, zeigt, daß die Cyclisierung der Polymeren mit BA und PCA in einem geringeren Umfang stattfindet. Die beiden letztgenannten Polymeren neigen also weniger zur Cyclisierung.
    Notes: Thermally polymerized samples of linear addition polymers of bisphenol-A-diglycidyl ether (DGEBA) and the following three different amines (A): benzylamine (BA), p-chloroaniline (PCA), and cyclohexylamine (CHA) were chromatographed by gelpermeation chromatography (GPC) using THF as eluent. The solvation effect of hydroxyl groups by THF has been taken into consideration when calibrating the system and interpreting the chromatograms. The comparison of the chromatograms suggests that the polymer with CHA is cyclized already in the range of small molecular masses (including dimers) and in an early stage of reaction. The comparison of average molecular masses of the samples as measured with independent methods - vapour pressure osmometry (VPO) and GPC - shows that the cyclization of the polymers with BA and PCA takes place to a lower extent, the latter polymer being less capable of cyclization.
    Additional Material: 8 Ill.
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  • 113
    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: Graft copolymers P(E-g-MMA) were prepared by ozonisation of low density polyethylene (LDPE) and grafting of methyl methacrylate (MMA) in bulk onto the peroxides and hydroperoxides thus obtained (Mn graft PMMA = 7700 and 21400). The emulsifying effect of P(E-g-MMA) copolymers on PE-PVC mixtures was examined. With added quantities of 5.0% copolymers the braking strength value σB for the mixture PE-PVC 50-50 is varying between 0.60 to 1.10 kg/mm2; the variation of the elongation at break point εB is more difficult to explain. The alloy fractographs were also examined under the scanning electron microscope. We observed PE modules of 20 to 30 in average diameter, without copolymer, and 1 to 2 after adding 5% of copolymers. This underlines the emulsifying role played by the copolymer. These results are compared with those of other teams. The P(E-g-MMA) that we prepared, can be considered as a suitable emulsifier for LDPE-PVC mixtures and presents the advantage of being more accessible for industrial synthesis of new alloys PE-PVC.
    Notes: Les copolymères greffés P(E-g-MMA) sont préparés par réaction du méthacrylate de méthyle (MMA) en masse sur le polyéthylène basse densité ozonisé. La masse moyenne des greffons de PMMA variable suivant la température et le temps de réaction est de 7700 et 21400. Ces copolymères sont testés comme émulsifiants de mélanges de PE et de PVC dont les propriétés mécaniques, la contrainte à la rupture σR, l'allongement à la rupture εR% et le module d'élasticité E sont mesurées avant et après l'addition de 5% en poids de copolymère. Pour le mélange PE-PVC 50-50 σR passe de 0,60 à 1,10 kg/mm2, la variation de εR est plus complexe. La visualisation, au microscope électronique à balayage, des fractographies de ces divers mélanges, montre une diminution d'au moins un facteur 10 de la taille des phases après addition de copolymère et confirme bien le rôle d'émulsifiant d'émulsifiant de ceux-ci permettant d'obtenir ainsi de nouveaux alliages PE-PVC dont les propriétés sont comparées avec celles d'alliages préparés par d'autres auteurs avec d'autres émulsifiants.
    Additional Material: 9 Ill.
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  • 114
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 162 (1988), S. 163-173 
    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: In dieser Arbeit wird die Effizienz einer neuen modifizierten Säulenfraktionierungsmethode durch Vergleich von theoretischen Modellen und experimentell erhaltenen Molmassenverteilungen vorgestellt. Fünf theoretische Funktionen wurden zur Anpassung der experimentellen Daten benutzt: die Log-normal-, Tung-, Schulz-, Polynomial- und Flory-Verteilungsfunktion. Die Kurvenanpassung wurde durch die mittlere quadratische Abweichung abgeschätzt. Die mittlere quadratische Abweichung war in allen theoretischen Modellen von der gleichen Größenordnung. Mit der Polynomial- und Flory-Funktion wurden die kleinsten Werte für die mittlere quadratische Abweichung und somit die beste Anpassung der aus der Gelpermeationschromatographie erhaltenen Verteilungskurven erreicht. Diese Kurven geben die wahre Verteilung der benutzten Polymeren wieder. Diese theoretischen Modelle dienten auch als Referenzverteilungsfunktionen. Die experimentell mit zwei verschiedenen LCIsungsmittelpaaren bestimmten Fraktionswerte wurden dann den ausgewlhlten Referenzmodellen angepdt. Die Fraktionswerte der beiden benutzten Lösungsmittelpaare stimmten gut mit dem Polynomial- und Flory-Modell überein. Dies bestätigt die hohe Effizienz der vorgeschlagenen Fraktionierungsmethode.
    Notes: In this paper the efficiency of a new modified column fractionation method was presented through the comparison of theoretical models and experimentally obtained molecular mass distribution. Five theoretical functions were used for fitting the experimental data: log-normal, Tung, Schulz, polynomial, and Flory distribution function. The curve fittings were estimated by the mean square deviation. The mean square deviations in all the theoretical models were of the same order. The least values of mean square deviation and consequentely the best fitting of the gel permeation chromatography (GPC) distribution curve, which deals as a true distribution of the applied polymer sample, were achieved with polynomial and Flory model. These theoretical models were further chosen as a reference distribution function. The experimental fractionation data in two quite different solvent pairs were afterwards fitted to the chosen referent models. Fractionation data of the both applied solvent pairs have been in close agreement with Flory and polynomial model. This confirms the high efficiency of the proposed fractionation method.
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  • 115
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 163 (1988), S. 23-35 
    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 Chlorierung von ataktischem Polypropylen (APP) wurde thermisch gestartet und in Tetrachlorkohlenstoff durchgeführt. Es wurde gefunden, daß mit zunehmender Verdünnung der Chlorierungsgrad steigt, was in % Gewichtszunahme gemessen wurde. Grund für dieses Verhalten ist eine größere Aufweitung und Beweglichkeit der APP-Ketten, wodurch die durch Chlor zu ersetzenden Stellen besser zugänglich werden. Die Reaktionsordnung in Abhängigkeit von der APP-Konzentration beträgt 0,84 und die Aktivierungsenergie (Er) 5,29 kcal/mol. Die Erhöhung der Strömungsrate führt zu einem höheren Chlorierungsgrad. Dieser steigt bis zu einer Strömungsrate von 1 l/h linear an, um dann ein konstantes Nivoau anzustreben. IR-Spektroskopie und 13C-NMR-Untersuchungen weisen darauf hin, daß die Chlorierung an allen drei ersetzbaren H-Atomtypen vorkommt. Der Startschritt des Mechanismus ist wahrscheinlich die Substitution des tertiären H-Atoms durch freie Chlorradikale und nachfolgendem Austausch der sekundären und primären H-Atome durch entweder fortschreitende Substitution oder den Eliminierungs-Additions-Mechanismus.
    Notes: Chlorination of atactic polypropylene (APP) was thermally initiated and carried out in carbon tetrachloride (CCl4) solution. It was found that with the increase in dilution, there is an increase in the extent of chlorination, as measured in terms of % weight-gain. The reason for this behaviour has been ascribed to a greater degree of opening up and mobility of APP chains thus increasing the accessibility of the replaceable sites to chlorine. The order of the reaction with respect to APP concentration was found to be 0.84, the overall activation energy (Er) being 5.29 kcal/mol. Increase in flow rate leads to an increase in the extent of chlorination and was found to be increasing linearly with a flow rate up to 1 l/h beyond which it levels off. IR spectroscopy and 13C-NMR studies indicate the chlorination occurring in all the three types of replaceable H-atoms in APP. The mechanism appears to be initial substitution of tertiary H-atom by free chlorine radical followed subsequently by replacement of secondary and primary H-atoms via either progressive substitution or elimination-addition mechanism.
    Additional Material: 8 Ill.
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  • 116
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 27 (1988) 
    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
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  • 117
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 27 (1988), S. 97-111 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The translational friction of a particle inside a rigid hollow sphere is determined in this work. This should be important in model studies of solute diffusion in cells or vesicles. An extended shell algorithm is developed and used in which the cell or vesicle is modeled as a large number of beads. In the extended algorithm, the shell is divided into groups of beads and the assumption is made that the force exerted by each bead on the solvent is constant within a group. The algorithm is tested by using it to determine the translational friction constants of spheres and prolate ellipsoids modeled as shells of beads.
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  • 118
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    Biopolymers 27 (1988), S. 113-122 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Spectroscopic measurements of three representative elapid toxins are presented. An analysis of the data leads to the conclusion that the 228-nm CD band in this class of proteins originates largely in the disulfide chromophore. The intensity of this CD band is sensitive to conformational change associated with the disulfide group.
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  • 119
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    Biopolymers 27 (1988), S. 157-163 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Variations I-XVIII of a trimerlike cross-linked collagen model peptide were synthesized and used to investigate the cooperation of different neighboring Gly-X-Y tripeptides. The carboxy-terminal decapentapeptide of the tripe-helical part of collagen type I was chosen as the starting point of sequentially modified elongations. The transition temperatures determined by CD measurements show that the incorporation of the imino acid free tripeptides Gly-Ala-Ala and Gly-Ile-Ala results in a weakening of the triple-helical structure. It is demonstrated that the desired thermal stability of the collagen triple helix requires the “clustered” arrangement of helix-promoting tripeptides, especially of Gly-Pro-Hyp.
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  • 120
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    Biopolymers 27 (1988), S. 139-155 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The effect of a number of tetramethylammonium salts on the equilibria and kinetics of the disorder to order transition in the polysaccharide κ-carrageenan have been investigated. Data from the temperature dependence of optical rotation show that anion stabilization of the ordered form follows the lyotropic series I- 〉 Br- 〉 NO-3 〉 Cl- 〉 F-. Stopped-flow polarimetry was used to study the kinetics of conformational ordering following a rapid increase in salt concentration. The transition to the new equilibrium position was shown to be biphasic for all of the tetramethylammonium salts studied. The rate equation for the fast phase and the temperature dependence of the observed forward rate constant accord with a cooperative dimerization process. Activation parameters for helix nucleation, ΔH* and ΔS*, vary with both salt concentration and (at constant ionic strength) the anion type, increasing through the lyotropic series from I- to F-. The slow phase shows second-order kinetics, and is interpreted as further stabilization of the ordered form either through limited aggregation or annealing. The rate constant for the slow phase also follows the lyotropic series. Thus we have shown that both the growth and nucleation processes are anion dependent.
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  • 121
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    Biopolymers 27 (1988), S. 187-200 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Using an iterative approach, we have placed monovalent (“solvated”) and divalent (both solvated and “unsolvated”) ions around a 20 base pair sequence, (dC-dG)10, in standard B and ZI conformations. The molecule with its attendant ions in the various conformations is subjected to to energy minimization using the program AMBER. In the presence of solvated cations (both monovalent as well as divalent) the B form is more stable than the Z form. However, direct binding with the unsolvated divalent cations makes the Z form more stable. Groove-binding provides some insight into the facility with which the B to Z transition occurs with higher charged cations. In the presence of unsolvated divalent cations, the Z form binds more charges at the groove through more ligands, compared to the B form. The orientation around the CpG phosphates in the minor groove of the Z form is found ideal for ion binding. Detailed molecular models for the ion binding have been developed. In general, phosphate groups dominate the ion binding. Large perturbations are seen mostly in the angles that control the phosphate orientation.
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  • 122
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The basic relations between the molar fractions and the scanning calorimetry data for the system that includes self-dissociation/association process such as \documentclass{article}\pagestyle{empty}\begin{document}$$ m_0 {\rm A}_{\rm 0} \mathbin{\lower.3ex\hbox{$\buildrel\textstyle\rightarrow\over {\smash{\leftarrow}\vphantom{_{\vbox to.5ex{\vss}}}}$}} m_1 {\rm A}_{\rm 1} \mathbin{\lower.3ex\hbox{$\buildrel\textstyle\rightarrow\over {\smash{\leftarrow}\vphantom{_{\vbox to.5ex{\vss}}}}$}} m_2 {\rm A}_{\rm 2} \mathbin{\lower.3ex\hbox{$\buildrel\textstyle\rightarrow\over {\smash{\leftarrow}\vphantom{_{\vbox to.5ex{\vss}}}}$}} ... \mathbin{\lower.3ex\hbox{$\buildrel\textstyle\rightarrow\over {\smash{\leftarrow}\vphantom{_{\vbox to.5ex{\vss}}}}$}} m_n {\rm A}_n $$\end{document} are presented, where mi is the stoichiometric coefficient of the ith state Ai. The relations are described for each state j as \documentclass{article}\pagestyle{empty}\begin{document}$$ \frac{d}{{dT}}\left[{- m_j \log f_j (T) + \sum\limits_i {m_i f_i (T)}} \right] = \Delta H_j (T)/RT^2 $$\end{document} where fj(T) is the molar fraction function of state j and ΔHj(T) is the difference enthalpy function of the system referred to the state j, which can be obtained by scanning calorimetry; R is the gas constant; and T is the absolute temperature. By these relations, scanning calorimetry data can be deconvoluted in order to determine the thermodynamic functions by means of single and double deconvolution. The concentration dependence of the data is analyzed by a method presented in this paper. The nonlinear least squares fitting method for the determination of the functions is discussed. For an example of the application of this method to the actual scanning calorimetry data, thermodynamic data of multistate thermal transition of Vibrio parahaemolyticus hemolysin are analyzed.
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  • 123
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: We have observed that the rate of folding of the enzymatically hydroxylated form of poly(Gly-Pro-Pro) into the triple-helical conformation is considerably higher than that of the unhydroxylated polypeptide [R. K. Chopra and V. S. Ananthanarayanan (1982) Proc. Natl. Acad. Sci. USA 79, 7180-7184]. In this study, we examine a plausible kinetic pathway for triple-helix formation by selecting peptide models for the unhydroxylated collagen molecule, and computing their conformational energies before and after proline hydroxylation. Starting with the available data on the preferred conformations of proline- and hydroxyproline-containing peptide sequences, energy minimization was carried out on the following pairs of peptides: Gly-Ala-Pro-Gly-Ala and Gly-Ala-Hyp-Gly-Ala; Gly-Pro-Pro-Gly-Ala and Gly-Pro-Hyp-Gly-Ala; Gly-Ala-Pro-Gly-Ala-Pro and Gly-Ala-Hyp-Gly-Ala-Hyp. It was found that, with each pair of peptides, the energetically most favorable conformation (I) has an extended structure at the Gly-Ala or Gly-Pro segment and a β-bend at the Pro-Gly or Hyp-Gly segment. In the Hyp-containing peptides, this conformation is further stabilized by a (Hypi + 2)OH…OC(Glyi) hydrogen bond. Conformation I is lower in energy by about 6-13 kcal/mol of the peptide than the fully extended conformations that resemble the single collagen polypeptide chain and contain no intramolecular hydrogen bond. In contrast to the proline counterpart, the hydroxyproline-containing peptides are found capable of adopting a partially extended conformation that does not contain the β-bend but retains the (Hyp)OH…OC(Gly) hydrogen bond. The energy of this conformation is intermediate between conformation I and the fully extended conformation. The continuation of the β-bend along the chain is restricted by stereochemical constraints that are more severe in the latter two pairs of peptides than in the first pair. Such a restriction may be considered to trigger the “unbending” of the minimum energy conformation leading to its straightening into the fully extended conformation; the latter, in turn, would lead to triple-helix formation through favorable interchain interactions. We propose that the partially extended conformation in the Hyp-containing peptides could serve as a kinetic intermediate on the way to forming the fully extended conformation. Because of the (Hypi + 2)OH…OC(Glyi) hydrogen bond, this conformation would also serve to lock the trans geometry at the Gly-Ala(Pro) and Ala(Pro)-Hyp peptide bonds, thereby enhancing the rate of their helix formation. A scheme for collagen folding in proposed on the basis of these results.
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  • 124
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    Biopolymers 27 (1988), S. 351-354 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
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  • 125
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The conformational preferences of the N-trifluoroacetylated homo-peptides of Cα,α-diethylglycine from monomer to pentamer in chloroform solution were determined by using ir absorption and 1H-nmr. Intramolecular hydrogen bonding was found to be the dominant factor for all NH groups. The likely absence of a conformational transition upon increasing main-chain length, and the remarkable stability to dilution, heating, and addition of perturbing agents, are additional relevant findings of this study. These results are in agreement with those of the fully extended, C5-conformation-forming homo-peptides from the higher homolog Cα,α-di-n-propylglycine, but contrast dramatically to those of the homo-peptides from the lower homolog Cα,α-dimethylglycine, which have been shown to adopt the 310-helical structure.
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  • 126
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    Biopolymers 27 (1988), S. 423-430 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The conformation of a 13-residue C-peptide analogue of ribonuclease A -  - in surfactant solutions was studied by CD. The CD spectrum of the peptide in excess NaDodSO4 solution was typical for a helical conformation; the spectrum appeared to be virtually independent of pH (2.5-6) and temperature (3-25°C). Analysis of the CD data indicated a helicity of about 65-70% with no α-sheet and β-turn; this corresponded to 8 or 9 residues in the helical form or slightly more than two turns of α-helix. This compares with an average of about one turn of α-helix for the C-peptide analogue in water at pH 4.7 and 7°C. The conformation of the peptide in cationic surfactant, dodecyl ammonium chloride, and nonionic surfactant, dodecyl heptaoxyethylene ether, solution resembled that in water. We concluded that the C-peptide analogue can develop a maximum helicity close to the corresponding segment in ribonuclease A in hydrophobic environment provided by the clustering of NaDodSO4 molecules to the cationic side groups of the peptide, except that the end effects may destabilize two or three residues each at both ends of the helix. Thus, in the interior of a protein molecule this hydrophobic effect may overshadow the charged-group effect than can be explained by the helix dipole model for the helical segments on the exterior of the protein molecule.
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  • 127
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    Biopolymers 27 (1988) 
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    Keywords: Chemistry ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology
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  • 128
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    Biopolymers 27 (1988), S. 561-584 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Matrix generator techniques have been adapted to account for precise structural features of the nucleotide repeating unit and to translate the primary sequence of DNA base pairs into three-dimensional structures. Chains have been constructed to reflect the local sequence-dependent differences of bending and twisting of adjacent residues and various overall chain properties, including the average unperturbed moments of the end-to-end vector r and the mean angular orientation (〈γ〉 between base pair normals, 〈φ1〉 between long axes, and 〈φ2〉 between short axes) of terminal chain residues, have been computed. The chain backbone is treated implicitly in terms of the spatial fluctuations of successive base pairs. Motions are limited to low-energy perturbations of the standard B-DNA helix. Approximate potential energy schemes are used to represent the rules governing the patterns of local base-base morphology and flexibility. Theoretical predictions are compared with experimental observations at both the local and the macro-molecular level. Initial applications are limited to the rodlike poly(dA) · poly(dT) and poly(dG) · poly(dC) helices. The former duplex is found to be more compressed and the latter more extended than random-sequence DNA of the same chain length. The flexibility of the duplexes as a whole is described in terms of the average higher moments of the displacement vector ρ = r - 〈r〉 and the likelihood of chain cyclization is estimated from the three-dimensional Hermite series expansions of the displacement tensors. Emphasis is placed on theoretical methodology and the practical relevance of the calculated chain moments to observed physical properties.
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  • 129
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    Biopolymers 27 (1988), S. 585-603 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The matrix-generator methods set forth in the preceding paper for treating rodlike DNA are adapted here to the calculation of average chain extension, macroscopic flexibility, and terminal residue orientation in curved duplexes. The different characteristics of curved vs rodlike chains are illustrated with the hypothetical poly[d(A5G5)] · poly[d(T5C5)] duplex. The curved helix is both more compact and macroscopically stiffer than either the poly(dA) · poly(dT) or the poly(dG) · poly(dC) chain. The calculations have also been extended to simple repetitive DNA sequences generated by synthetic ligation studies and the computed average chain properties compared with observed gel mobilities. The predicted chain extension is also checked against the measured persistence lengths of the rodlike poly[d(GC)] and poly[d(AT)] alternating copolymers, and the known cyclization tendencies of selected repeating sequences. Chains are generated from local potential energy maps describing the morphology and flexibility of adjacent base pairs. The energy maps, while approximate, are more accurate descriptors of local structure than many of the intuitive models of DNA curvature offered to date. According to the energy surfaces, the intrinsic bending of curved DNA can be traced to asymmetry in the bending of the Gs and Cs that join half-helical turn stretches of adenines in these chains. The oligo A stretches are analogous to residues of a perfectly elastic DNA that bend with equal likelihood in opposing directions. In other models of DNA curvature, the (G · C) base pairs are presumed to adopt the classical B-DNA structure, while the (A · T) base pairs are thought to be in some perturbed conformation.
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  • 130
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    Biopolymers 27 (1988) 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 131
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 1H-nmr studies were extensively carried out to elucidate preferred conformations of dipeptides CH3C*O - X - NHCH3, with X = Abu, nVal, and Val in various solvents. The vicinal 1H - 1H coupling constants for the NH - CαH moiety and those around the Cα - Cβ bond in the articulated side chain provided the information regarding the average conformation of these molecules. The results indicate that transformation of skeletal conformations takes place in solution among conformers having similar dihedral angles, θHN - CαH, in the Karplus expression.
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  • 132
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    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: High-resolution 1H-nmr spectroscopy at 500 MHz has been used to study the Ca2+ binding domain I of bovine brain calmodulin in aqueous solution. All the resonances of the linear dodecapeptide Asp-Lys-Asp-Gly-Asn-Gly-Thr-Ile-Thr-Thr-Lys-Glu and of its cyclic analogue, synthesized by classical solution methods, have been completely assigned using a combination of several one- and two-dimensional nmr experiments, including the zero quantum correlation. Chemical shift values and 3JCHNH coupling constants indicate that, on the nmr time scale, both peptides are flexible and assume multiple conformations in rapid equilibrium, with no relevant contribution of structured features. Addition of Ca2+ causes only minor spectral changes in aqueous solution of both peptides, while larger effects are observed in more hydrophobic mixtures such as water/trifluoroethanol. The linear analogue shows nonspecific interactions, while only Asp3 and Asn5 are significantly perturbed in the cyclic peptide. This evidence, together with identical findings in La3+ titration studies of the cyclic analogue in pure water, suggest that loop I of calmodulin is endowed with an intrinsic binding ability.
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  • 133
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    Biopolymers 27 (1988), S. 831-842 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The interactions of the antitumor antibiotics, chromomycin A3, with a variety of metal cations in the pH range of 3.0-8.5 were systematically studied by CD, absorption, and 1H-nmr spectroscopies. Results were compared with those obtained in the presence of increasing amounts of calf thymus DNA. The negatively charged chromomycin A3, pKa 6.3, forms aggregates that become ordered and smaller in size, in the presence of variety of metal cations. Spectrophotometric titrations have shown that binding of the neutral drug to DNA at pH 4.5 does not require divalent cations, although the strength of the binding is greatly enhanced in their presence. At higher pH values (〉 7.0) and low DNA/drug ratio ( 〉 20), the metal cations are necessary to induce the binding between chromomycin A3 and DNA. At higher DNA/drug ratios (〉 100: 1), an appreciable proportion of the drug is bound even in the absence of divalent cations. Its binding affinity to the DNA is enhanced in the presence of these cations and at low pH values. Therefore, we conclude that chromomycin A3 binds in two related modes, in the presence and in the absence of divalent cations. The spectral data accumulated indicate the metal cation is involved in the binding of the drug to the DNA by forming a drug-metal-DNA ternary complex.
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  • 134
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Bands in the ir and Raman spectra of L-valyl-glycyl-glycine (VGG) and VGG-ND have been assigned on the basis of a normal mode analysis of the known parallel-chain β-structure of this tripeptide. Amide I, II, III, and V mode shifts are obtained by the interactions of dipole derivatives in symmetry coordinates, referred to as dipole derivative coupling. These derivatives, obtained from ab initio studies, are also used to calculate ir intensities of amide I, II, and V modes. The agreement between predicted and observed frequencies and intensities is very good, providing confidence in the application of our force fields to the calculation of the vibrational modes of the general parallel-chain β-sheet structure (following paper).
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  • 135
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    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The tetrapeptide Gly-Pro-Arg-Pro(GPRP) was introduced by diffusion into fine unligated clots formed from human fibrinogen at pH 8.5 and ionic strength 0.45 by batroxobin (αβ-fibrin) and by thrombin (α-fibrin). The α-fibrin clots were essentially liquefied at GPRP concentrations above 1 mM and αβ-fibrin clots above 15 mM, and the degree of polymerization of the resulting oligomers decreased progressively with increasing GPRP concentration as shown by γ-γ ligation with factor XIIIa and subsequent gel electrophoresis. Much smaller concentrations of GPRP, when introduced into unligated clots by diffusion, were sufficient to modify their mechanical properties profoundly. The shear modulus of elasticity G25 measured 25 s after imposition of stress fell, for example, by a factor of 0.4 at 0.1 mM GPRP in α-fibrin and at 1.1 mM in αβ-fibrin. The rate of shear creep under constant stress and the proportion of irrecoverable deformation also increased enormously. This behavior, and the corresponding decrease in steady flow viscosity, may be interpreted in terms of competition of GPRP with A sites on the E domains of fibrin monomers for bidning to “a” sites on the D domains, resulting in a moderate increase with increasing GPRP concentration of the average proportion of severed network strands and an enormous increase in the rate at which all strands dissociate and reassociate. Reassociation of severed strands in new configurations is a necessary corollary since the differential modulus or compliance remains constant during creep and creep recovery. The greater susceptibility of α-fibrin clots to interaction with GPRP is attributed to stabilization of contacts between monomer units by Bb associations in αβ-fibrin. Ligated clots, with or without GPRP, exhibited essentially no time-dependent creep and no irrecoverable deformation, corresponding to an absence of any severance of network strands.
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    Biopolymers 27 (1988), S. 939-956 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Molecular dynamics simulations have been used to study the conformational fluctuations of the oligopeptide hormone vasopressin. Starting coordinates for these simulations were built upon the crystal structure of pressinoic acid, the cyclic ring moiety of vasopressin, recently determined by x-ray diffraction. Coordinates for the additional tripeptide “tail” of vasopressin were selected by arbitrary positioning of this segment using interactive computer graphics. Two such starting configurations were minimized to relax strains, and long dynamics simulations (20 and 40 ps) in vacuo were then conducted following extensive heating and equilibration sequences (36 ps). In these studies, vasopressin was found to undergo few substantial conformational changes at 300 K on the time scale simulated, in contrast to the results of a shorter previous simulation, but comparable structural transitions were observed during the equilibration periods. The pressinoic acid structure was found to be a reasonably stable possible conformation for vasopressin in vacuum on this time scale.
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  • 137
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    Biopolymers 27 (1988), S. 1045-1051 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 138
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new approach to the multiple-minima problem in protein folding is presented. It is assumed that the molecule is driven toward the native structure by three types of mechanism. The first one involves an optimization of the electrostatic interactions, whereby the molecule evolves toward conformations in which the charge distribution becomes energetically more favorable. The second mechanism involves a Monte Carlo-energy minimization approach, and the third one is a backtrack mechanism that acts in the opposite direction, increasing the energy - the third type of movement provides a means to perturb the molecule when it is trapped in a stable but energetically unfavorable local energy minimum. This paper describes the implementation of a model based on these mechanisms, and illustrates its effectiveness by computations on different arbitrary starting conformations of a terminally blocked 19-residue chain of poly(L-alanine) for which the global minimum apparently corresponds to the right-handed α-helix. In all cases, the global minimum was attained, even when the starting conformation was a left-handed α-helix. In the latter case, the trajectory of conformations passed through partially melted forms of the left-handed α-helix (because of electrostatic defects at the ends), and then through the formation of structures leading to the more stable right-handed α-helix.
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  • 139
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    Biopolymers 27 (1988), S. 1641-1654 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Weight-average molecular weights Mw, second virial coefficients, and z-average radii of gyration 〈S2〉1/2z were determined by light scattering as a function of temperature T for four sodium salt samples of xanthan in 0.01M aqueous NaCl, in which the polysaccharide undergoes an order-disorder conformation change with increasing T. The data for 〈S2〉1/2z and Mw at 25 and 80°C, the lowest and highest temperatures studied, confirmed the previous conclusion that the predominant conformation at the former T, i.e., in the ordered state, is a double helix, while that at the latter T, i.e., in the disordered state, is a dimerized coil expanded by electrostatic repulsions between charged groups of the polymer. As T was increased from 25 to 80°C, 〈S2〉1/2z sigmoidally decreased or increased depending on the dimer's molecular weight. This temperature dependence of 〈S2〉1/2z and that determined elsewhere for a high molecular weight sample were found to be described almost quantitatively by a simple dimer model in which the double helix melts from both ends, when the double-helical fraction in the dimer at a given T estimated previously from optical rotation data was used.
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  • 140
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    Biopolymers 27 (1988), S. 1687-1690 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 141
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    Biopolymers 27 (1988) 
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    Keywords: Chemistry ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology
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    Biopolymers 27 (1988), S. 1491-1517 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Intercalated complexes of the antitumor antibiotic nogalamycin (NGM) with the double-stranded oligonucleotides d(GCGC)2, d(ATAT)2, and d(ACAC) · d(GTGT) are investigated with the theoretical method SIBFA. The amino sugar part of the drug locates preferentially in the minor groove. An intrinsic preference for the d(ATAT)2 sequence over the d(ACAC) · d(GTGT) and d(GCGC)2 sequences is obtained, corresponding to relative energies 0, 11, and 15 kcal/mole, respectively. A mixed sugar-puckering pattern is preferred in the d(ATAT)2 complex while a uniform sugar-puckering pattern is preferred for the other sequences. No direct specific interaction involves the N+ - H part of protonated NGM. The location of the amino sugar as well as the sequence selectivity is due to the global electrostatic interaction of the dimethylammonium group with the given groove. The two hydroxyl groups of the amino sugar and the carbonyl of the carbomethoxy group encounter partners for hydrogen bonding at the intercalation site, but these interactions do not appear to govern the base sequence selectivity. The nogalose part is not found to be directly involved in the binding or in the selectivity. The conformations of isolated and intercalated NGM are discussed.
    Additional Material: 11 Ill.
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  • 143
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polymerization of fibrin molecules results in the formation of a double-stranded protofibril. Although convincing data have not been presented, it is classically believed that γ-chain cross-linking of fibrin molecules occurs between the longitudinal end-to-end contacts (DD-long contacts) of the molecules within each of the two strands of a protofibril (intrastrand cross-linking). In this investigation the question addressed was whether γ-chain cross-linking takes place across the two strands (interstrand cross-linking) between the transversal half-staggered contacts of the molecules. Demonstration of double-stranded protofibrils in the presence of urea would indicate an interstrand cross-linking, whereas in the case of intrastrand cross-linking, the chaotropic agent urea would dissociate the double-stranded structure to form single-stranded fibrils. Protofibrils were obtained by generating soluble cross-linked fibrin polymers (sXLFbP): After incubation of souble fibrin polymers with Factor XIIIa at 37°C, the polymerization and cross-linking reaction was stopped by the addition of 6M urea and EDTA. Gel filtration of the reaction mixture in the presence of 3M urea was effect in separating sXLFbP from monomeric molecules. The sXLFbP-containing fractions were adsorbed onto mica in the presence of different concentrations of urea and investigated by electron microscopy after rotary shadowing. In the presence of 3M urea the sXLFbP appeared as double-stranded protofibrils. In the presence of 4M urea some parts of the double-stranded structure were found to be unfolded whereas in the presence of 6M urea multiple-bended single-stranded fibrils were observed. SDS-polyacrylamide gel electrophoresis of the sXLFbP demonstrated no γ-chain cross-linking within the protofibrils. Ultracentrifugation of the sXLFbP showed that in the presence of 3M urea noncross-linked fibrin polymers dissociated to monomeric molecules. When sXLFbP was centrifuged into 6M urea on sucrose density gradients, no reduction of the polymer size could be observed. The data indicate that γ-chain cross-linking occurs between the transversal contacts of the fibrin molecules within a protofibril, thus generating interstrand cross-linking. A model of the cross-linking of polymerized fibrin molecules is developed and the term DD-trans contact is proposed for this specific alignment of the D-domains.
    Additional Material: 9 Ill.
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  • 144
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A general treatment for the solution dynamics of segmentally flexible macromolecules having two subunits is presented. Bead modeling allows for a complete inclusion of hydrodynamic interactions in this treatment. The finite size of the beads is also considered, so that it is therefore possible to account properly for torsional motions of the subunits. Expressions for the components of the resistance matrix are derived. From them, the translational and rotational diffusion coefficients can be calculated. Distinction is made between hinged macromolecules, whose only internal motion is bending, and swivel-jointed macromolecules, for which torsions of the subunits are also allowed. Numerical results are presented for broken rods with the two types of flexibility. The effects of hydrodynamic interaction between arms of broken rods are about 25% for translation and under 10% for rotation. These findings give support to the treatments of Harvey, Wegener, and co-workers in which interactions were neglected. The rotational dynamics of hinged and swivel-jointed rods are compared. Although there are differences in the short-time behavior, the longest relaxation time is the same for the two cases. Finally, the validity of Wegener's rotational diffusion constants is discussed.
    Additional Material: 4 Ill.
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  • 145
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    Biopolymers 27 (1988), S. 1831-1838 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Cluster analysis techniques were used to examine a set of Fourier transform infrared (FT-IR) spectra of bovine serum albumin (BSA) in the adsorbed and nonadsorbed states. The region from 1480 to 1600 cm-1, comprising the amide II band, was used. Spectra were preprocessed to compensate for linear baseline variation, and the single linkage method of cluster analysis was applied. As expected, the spectra of adsorbed and nonadsorbed BSA fell into two distinct clusters. However, no further clustering was observed among the adsorbed BSA spectra on the basis of surface type, suggesting that surface specificity of the spectral changes induced in BSA by adsorption is not detectable above experimental variation. This work illustrates the value of using cluster analysis in the FT-IR study of proteins as a complement to other data analysis methods.
    Additional Material: 4 Ill.
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  • 146
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    Biopolymers 27 (1988), S. 1749-1760 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The ir spectra of lathyritic rat skin collagen and calf skin gelatin solutions at a variety of temperatures were obtained using Fourier transform ir spectroscopy and a 9-reflection, 2-pass ZnSe prism sample cell. The spectra were then deconvolved (based on Kauppinnen's method) and the behavior of the amide I band at ∼ 1650 cm-1 observed in detail. Throughout the temperature range studied (4-50°C), three component absorption peaks within the amide I band (at 1633, 1643, and 1660 cm-1) are common to the spectra irrespective of the degree of triple helix content of the sample. Changes in the relative intensities of these component peaks are, however, conformationally dependent. During denaturation of the triple helix, the dominant 1660-cm-1 component in the native collagen spectrum diminishes and the 1633-cm-1 peak becomes relatively intensified. The inherently strong basicity of the carbonyl group of the proline residues together with the frequent occurrence of this imino acid in the X position of the Gly-X-Y triplet of collagen largely accounts for the -30-cm-1 shift of the amide I band during denaturation. Temperature and conformationally dependent changes in the fine structure of the amide I band from dilute solutions of collagen can be monitored in a reproducible and quantitative fashion.
    Additional Material: 6 Ill.
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  • 147
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    Biopolymers 27 (1988), S. 1787-1793 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Dielectric relaxation studies of bovine ligamentum nuchae are reported over the frequency range of 1 MHz to 1 GHz and over the temperature range of 23-48°C. A temperature-dependent relaxation process was observed at low megahertz-frequency with the correlation time of around 40 ns. The result is quite similar to that of a synthetic polypentapeptide (VPGVG) and of α-elastin. The relaxation is proposed to arise in part from the peptide libration within the polypentapeptide of bovine ligamentum nuchae.
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  • 148
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    Biopolymers 27 (1988), S. 1817-1829 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The bands within the range of 800-850 cm-1 of Raman spectra of polynucleotides sensitive to the change in conformation of sugar-phosphate backbone are analyzed theoretically. The bands are interpreted as the appearance of a quasi-local deoxyribose vibrational mode whose frequency is dependent on the ring puckering. The localization region of the vibrational mode is pointed out. The theory establishes a relationship between the observed spectral intensity and the population of deoxyribose conformational states described in the framework of the pseudorotation concept. The approach developed allowed one to describe the band shapes and their temperature behavior, and to determine the pseudorotation potential of deoxyribose in the helix B-form of A · T containing polynucleotides. Using the analysis of Raman spectra of DNA fibers in water-ethanol mixture the deoxyribose flexibility during the B-A transition is investigated in terms of the population of conformers and effective potential. It is shown that N- and S-type deoxyribose conformers are populated in the DNA B-form (those of the S-type are preferable), whereas N-type conformers are primarily populated in the DNA A-form.
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  • 149
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    Biopolymers 27 (1988) 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 150
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    Biopolymers 27 (1988), S. 1887-1896 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The crystal structure of L-lysyl-L-alanyl-L-alanine hydrochloride has been determined by x-ray diffraction. The peptide is in zwitterionic form with the carboxylic group deprotonated, and with positive charges both in the amino terminal and ∊-amino groups of lysine. Crystals are monoclinic, space group P21 and Z = 4, with two peptide molecules in the asymmetric unit, which show different conformations. While one molecule has torsional angles for the Lys-Ala peptide bond (ϕ2, ϕ2) in the β-pleated sheet region, the values for the other molecule are close to those for the α-helix. This molecular flexibility is of interest for the study of H1 histone, which contains this sequence repeated several times. The two lysine residues show fully extended side chains. Two methanol molecules and two acetonitrile molecules are also present in the unit cell. An extensive network of hydrogen bonds and ionic interactions stabilize the crystal structure.
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  • 151
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    Polymer Engineering and Science 28 (1988) 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
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  • 152
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    Polymer Engineering and Science 28 (1988), S. 413-420 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: This paper presents the development of the boundary element equations for the compression molding process of isothermal Newtonian fluids. It shows the numerical implementation of the boundary element equations and presents a simple method of carrying out the domain integral present in the governing equations. The results and accuracy of a boundary element simulation are discussed, and the numerical results compared to experimental values.
    Additional Material: 14 Ill.
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  • 153
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    Polymer Engineering and Science 28 (1988), S. 605-609 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The static delamination behavior of graphite/epoxy composite specimens subjected to mode I tensile opening (using UDCBUniform double cantilever beam. specimens), and pure mode II shear loading (using ENFEnd-notched flexural. specimens) were studied. The graphite epoxy composites for the study were made from commercially treated fibers, with and without an electropolymerized interlayer. The mode I fracture energy (GIC) was found to be significantly higher (more than 50 percent) for the coated fibers. However, this improvement was accompanied by a high reduction (more than 3 times) in the mode II fracture energy (GIIC). This effect is apparently related to poor adhesion between the interlayer and the epoxy resin, which may be corrected by use of a “top layer” of appropriate composition to form chemical bonds between the phases. The fracture toughness (KIC) of composites made with commercially treated fibers was also evaluated, using double side-notched specimens.
    Additional Material: 6 Ill.
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  • 154
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    Polymer Engineering and Science 28 (1988), S. 583-591 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: An analytical methodology was developed capable of describing interrelations between thermal processing and polymer structure for thermoplastic based composite laminates. Specifically, this modeling methodology was used to describe experimental results generated with a specially designed match die quench mold by processing both neat PEEK polymer and carbon fiber reinforced laminate samples at different cooling rates. The developed model accurately predicted temperature profiles for PEEK laminates of different thicknesses, under normal as well as extreme quenching conditions of 114°C/s. surface cooling rates that are possible to generate with the quench mold. In general, the modeling methodology is capable of predicting a part's thermal profile during processing in terms of the composite's microscopic intrinsic properties (fiber and matrix), composition, and lamina orientation. Furthermore, by coupling to the thermal profile description, a previously developed crystallization kinetics model for PEEK polymer and its carbon reinforced composite, a quantitative description of structural development during processing was obtained. Thus, with this analytical methodology, a skin-core crystallinity profile, where the crystallinity varies with part-thickness as a result of uneven cooling experienced during processing, was predicted both for the neat PEEK polymer and its carbon reinforced laminate forms. Finally, the developed methodology clearly established the interplay of both microscopic heat transfer and kinetics of crystallization/solidification of the matrix that must be accounted for in predicting the final structure of a carbon fiber reinforced laminate that will, in turn, govern microscopic and macroscopic performance.
    Additional Material: 7 Ill.
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  • 155
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    Polymer Engineering and Science 28 (1988), S. 634-639 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Neat poly(ether-ether-ketone) (PEEK) and carbon fiber reinforced PEEK (APC-2) specimens were prepared using a variety of cooling rates to achieve a range of crystallinities. Amorphous specimens were exposed to a variety of fluids to determine the penetrant types which are able to strongly influence the material. This allowed the estimation of the solubility parameter and hydrogen bonding index for PEEK to be 9.5 and 3.1, respectively. Methylene chloride was used to investigate the kinetics of penetrant sorption. The data demonstrated Case II behavior, with the initial crystallinity having a pronounced effect on both the kinetic and equilibrium data. Accordingly, a model was proposed capable of describing the sorption level and penetration depth as a function of time given the sample crystallinity and sorption temperature. With Case II behavior there was no difference in the sorption kinetics of neat and fiber reinforced PEEK. Finally, the dynamic mechanical properties measured during sorption were found to be dependent on the sorption process.
    Additional Material: 8 Ill.
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  • 156
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    Polymer Engineering and Science 28 (1988), S. 670-678 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The dynamic shear viscosity and the morphology of polypropylene homopolymer and copolymer blended with linear low density polyethylene are studied. A maximum in the dynamic shear viscosity vs. blend composition is reported for the polypropylene copolymer, linear low density polyethylene system. The increasing dynamic shear viscosity is in accordance with the occurrence of a morphology of polyethylene inclusions in rubber surrounded by a polypropylene matrix. Comparing calculations of the dynamic shear viscosities - based on a shell model with interlayer - and experimental results supports this view.
    Additional Material: 17 Ill.
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  • 157
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    Polymer Engineering and Science 28 (1988), S. 684-687 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Hydroxy-terminated copoly(fstyrene-b-1,2-butadiene) (HPSB) containing rubber-affinitive vinyl side chains and having a molecular weight of 2000 to 4000 were prepared, and block copolyurethanes were synthesized by using a low molecular weight hydroxy-terminated poly (ethyl en e terephthalate) as a PET-affinitive component and 4,4′-diphenylmethane diisocyanate as a chain extender. The relationships between the molecular weight of HPSB, copolymerization ratio of styrene to butadiene and the adhesive strength of PKT/rubber in high temperature atmospheres were examined. A peak of adhesive strength was observed at styrene copolymerization ratio of 20 wt percent and a HPSB molecular weight of 3000. The adhesion mechanism was estimated from the behavior of the characteristic infrared absorption of block Copolyurethane in heating.
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  • 158
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    Polymer Engineering and Science 28 (1988), S. 718-727 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: In vibration welding of thermoplastics, frictional work done by vibrating two parts under pressure, along their common interface, is used to generate heat to effect a weld. The main process parameters in vibration welding are the weld frequency, the amplitude of the vibratory motion, the weld pressure, and the weld time. How these parameters affect weld quality, the conditions that result in the best welds, the weldability of dissimilar plastics, and the effect of fillers such as glass are of interest. To address these issues, a research vibration welding machine in which all the parameters can be independently and accurately controlled and monitored was designed and fabricated. The phenomenology of welding, as determined by experiments on the four thermoplastics polycarbonate, poly (butylene terephthalate), polyetherimide, and modified poly (phenylene oxide), is described.
    Additional Material: 19 Ill.
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  • 159
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    Polymer Engineering and Science 28 (1988), S. 743-757 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: An engineering analysis of the reactive extrusion process of a thermoplastic polyurethane was made through numerical simulation and actual experiment. The reactants used in this system were 4,4′diphenylmethane diisocyanate, polycaprolactone diol (M.W., 824), and 1,4-bu-tanediol with equivalent weight ratio of 2:1:1. As a catalyst, dibutyltin dilaurate was used. The reaction kinetics and the viscosity function were obtained through experiments, and the mathematical model which includes the conservation equations of mass, momentum, energy, and chemical species was solved numerically to obtain the velocity, concentration, temperature, viscosity, and pressure profiles. The actual experiments were performed in the laboratory scale extruder to compare the experimental results with those of the numerical simulation.
    Additional Material: 30 Ill.
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  • 160
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    Polymer Engineering and Science 28 (1988), S. 775-784 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A series of polyurethane-urea/polyvinyl simultaneous interpenetrating polymer networks (SINs) were prepared starting from a mixture of isocyanate prepolymer blocked with N-(1-1′-dimethyl-3-cxobutyl) acrylamide oxime, chain extender, vinyl monomers, and catalysts. Their physical properties and morphology were investigated using differential scanning calorimetry, dynamic mechanical measurements, and small-angle X-ray scattering. The polyurethane-urea networks examined were two-phase in nature. The vinyl network was formed with diacetone acrylamide oxime, trimethylolpropane trimethacrylate, and N-vinyl-pyrrolidone. Calorimetric analyses revealed that the polyether soft segment phase separated within the SINs. At higher temperature, dynamic mechanical measurements demonstrated the presence of only one glass transition temperature (Tg) intermediate in temperature to the Tg of the vinyl network and the Tg of the urethane hard phase. This is indicative of chain entanglement (interpenetration) between the vinyl network and the polyurethane hard segments resulting in a two-phase morphology. Small-angle X-ray scattering analyses provided measurements of diffuse phase boundary thickness, phase mixing, and domain size distribution. Appreciable interfacial thickness was not observed and thus phase mixing occurred within the phases. Domain size distribution indicated that high network constraints hindered the development of domains and limited the phase segregation.
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  • 161
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    Polymer Engineering and Science 28 (1988) 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
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  • 162
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    Polymer Engineering and Science 28 (1988), S. 1152-1155 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Effects of absorbed moisture on degradation behavior of high nitrile barrier polymers were monitored using thermogravimetric analysis techniques. Non-modified and 10 percent rubber modified samples were heated isothermally at nitrile processing temperatures (200°C to 240°C) in air and nitrogen environments. Degradation was evaluated in terms of weight loss as a function of heating time and sample coloration. It was determined that complete removal of moisture, as well as high moisture concentration, contribute to increased degradation at the temperatures evaluated. Moisture levels in the range of 0.15 to 0.5 percent were found to minimize degradation. Heating environment, time, temperature, and rubber modification were also found to influence thermal stability.
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  • 163
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    Polymer Engineering and Science 28 (1988), S. 1167-1172 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: High density polyethylene has been chlorinated by three different methods: in suspension and in solutions of two different solvents. Carbon-13 NMR and infrared analysis show that chlorination in chlorobenzene solution leads to statistically random distribution while chlorination in suspension gives highly blocky substitution. An intermediate distribution was obtained by chlorination in tetrachloroethane solution.
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  • 164
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    Polymer Engineering and Science 28 (1988), S. 1198-1202 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The energy stored in polystyrene after plastic deformation is measured by the differential scanning calorimetry (DSC) technique. Similar to metals, the stored energy increases with plastic straining, first rapidly, and then more slowly, and finally the stored energy seems to approach a saturation value (about 1 cal/gram). By comparing to the plastic work done, the fraction stored ranges from 30 percent after 10 percent compression to 10 percent after 60 percent compression. The fraction is about twice as large as that of copper. The release of stored energy has two distinct parts, one below Tg and the other above Tg. Most of the strain recovery seems to accompany the second part. By using the Kissinger plot, the second part has an activation energy, of 142 kcal/mole which is about 10 percent larger than that of compressive strain recovery.
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  • 165
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    Polymer Engineering and Science 28 (1988), S. 1219-1226 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A trial and error approach reflects the state of the art in reaction injection molding. Material and process parameters determine the “moldability” of a specific system in a particular application. The concept of “molding areas” on the critical parameters plane can be extended form thermoplastic injection molding (TIM) to reaction injection molding (RIM).In this work moldability diagrams for the filling and curing stages of a RIM process are obtained based on a simplified engineering approach. The key process parameters chosen for the filling stage are initial material temperature and filling time. In the curing stage, the critical parameters are considered to be mold wall temperature and demold time. Experimental results obtained on a laboratory-scale RIM machine on a Crosslinking polyurethane system are used to check the validity of the predicted molding areas. The agreement obtained is satisfactory considering the broad range of processing parameters used.
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  • 166
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The microstructure of injection molded bars (2.9 and 5.8 mm thick) of thermotropic liquid crystalline poly(p-hydroxy-benzoic acid-co-ethylene terephthalate) has been studied by SEM on samples etched with n-propylamine, SEM fractography, DSC, IR, ESCA, WAXS and polarized microscopy. The 2.9 mm bar consists of three different layers: a highly oriented surface skin, an oriented intermediate layer and a non-oriented core. The 5.8 mm bar has a more complex microstructure and is composed of five different layers: a highly oriented surface skin, an oriented layer just beneath, a non-oriented layer, another oriented layer and a non-oriented core. The thicknesses of the different layers vary, significantly, with distance from the mold gate. The thickness of the core increases, significantly, with increasing distance from the mold gate at the expense of the oriented layers. The structure within the different morphological layers is not perfectly uniform. Tensile testing demonstrated the mechanical anisotropy of the surface material (a ratio of almost 20 between the longitudinal and transverse moduli) and the isotropy of the central core material.
    Additional Material: 15 Ill.
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  • 167
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    Polymer Engineering and Science 28 (1988), S. 1264-1269 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Rolling-drawing is a simple, effective, solid state processing technique for manufacturing high strength and high modulus oriented polymer sheet products. The process is capable of increasing the tensile modulus and strength of polypropylene by more, than an order of magnitude with inexpensive equipment and straight forward controllable techniques. This paper gives an overview of the rolling-drawing of polypropylene. It is intended to answer the following questions. What is rolling-drawing? What changes in tensile properties can be expected as a result of this process? What deformation processes occur during rolling-drawing? What are the processing variables and how do these variables relate to the deformation ratio achieved by rolling-drawing? A tensile flow stress relationship was formulated from experimental data for oriented polypropylene. This constitutive equation, estimates the flow stress (or yield stress) of the polymer as a function of deformation ratio, strain rate and temperature. Since stretching was found to provide a significant portion of the deformation during the rolling-drawing process a Hoffman-Sachs computer analysis was written to predict plastic deformation and drawing forces in the stretch zone. The results of experimentation and the analysis are briefly compared in this paper.
    Additional Material: 8 Ill.
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  • 168
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: An extrusion-grade of high density polyethylene (HOPE) (3 ethyl groups per 1000 carbons) has been divided into 16 fractions by preparative GPC and selective p-xylene extraction. The fractions, with molecular weights ranging from 900 to 1,000,000, have been studied by IR spectros-copy, DSC, WAXS, polarized microscopy, and small-angle light scattering (SALS), The average degree of chain branching (percent C2H5) is 0.5 percent for the part of the sample having a molecular weight lower than 10,000 and it decreases monotonically with increasing molecular weight, finally approaching 0.1 percent C2H5. A crystallinity depression with respect to linear PE equivalent to 20 percent/(percent C2H5) is recorded for all samples except for the very low molecular weight samples for which the crystallinity depression is much larger (30 to 35 percent/ (percent C2H5)). The unit cell volume increases with increasing percent C2H5, presumably due to the inclusion of ethyl groups in the crystals as interstitlals at 2gl kinks. The concentration of ethyl groups in the crystals (∊c) unanimously follows the relationship: ∊c(percent) = 0.32 + 0.25 log(percent C2H5) except for the low molecular weight fractions which have significantly lower values for ∊c. Our admittedly speculative explanation for this major discrepancy between high and low molecular weight samples is based on the idea that segments with ethyl groups close to chain ends have a greater difficulty in crystallizing than segments containing ethyl groups located at positions far from the chain ends. The fractions obtained from the extrusion-grade HDPE show a solidification temperature depression with respect to linear PE which can only be explained by the presence of chain branches in these samples. The depression is particularly pronounced for the low molecular weight samples as is expected from the data on molecular structure. Well-developed non-banded spherulites are observed in rapidly cooled (crystallized at about 35 K supercooling), low molecular weight samples (6,000 〈 Mw 〈 8,000)from the extrusion-grade HDPE in contrast to the axialites observed in linear PE of the same molecular weight and thermal treatment. This discrepancy in morphology has been related to the presence of ethyl groups in the extrusion grade HDPE fractions. Higher molecular weight samples (20,000 〈 Mw 〈 1,000,000)from the extrusion-grade HDPE and linear PE both display well-developed banded spherulites of similar nature as is expected due to the similarity in molecular structure of the two sets of sample.
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  • 169
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    Polymer Engineering and Science 28 (1988), S. 1066-1070 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: In this work, a concept of distributed damage, including its inception and propagation, was applied to creep induced buckling of specimens prepared from high density polyethylene (HDPE). Using a kinetic relationship for damage accumulation, an integral equation for the front of the damage zone was derived. A time parameter associated with the inception of the damage front was obtained. The motion of the front was approximated for small times. Long time estimation was obtained using an assumption for a shape of the damage distribution. These results enabled us to review reported experimental results on creep induced buckling using a new insight into the relationship between applied load and time to buckle.
    Additional Material: 6 Ill.
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  • 170
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    Polymer Engineering and Science 28 (1988), S. 1095-1106 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: We present a basic study of the thermal, dielectric, Theological, and mechanical properties of hydroxybenzoic acid-ethylene terephthalate copolymers (PHB-PET). It is argued that they have two-phase structures, one rich in ethylene terephthalate (PET) and one rich in hydroxybenzoic acid (PHB). Polystyrene (PS) is immiscible in 60% PHB-PET (60-PHB-PET) blends. Polycarbonate (PC) is partially miscible with the high PET phase of 60-PHB-PET. PET seems completely miscible with this high PET phase. Shear viscosity measurements on blends indicate that 60-PHB-PET gives rise to large reductions of viscosity. Extrudates and melt-spun fibers have been prepared. The phase morphologies of low PHB-PET blends as determined by scanning electron microscopy indicate ellipsoids or long fibrils of the, 60-PHB-PET in PS or PC matrices. High extrusion rates and melt spinning produce fibrillar structures. The mechanical properties of films, extrudates, and melt-spun fibers were studied. Blends with 10% 60-PHB-PET exhibited significant increases in Young's modulus and tensile strength.
    Additional Material: 29 Ill.
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  • 171
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    Polymer Engineering and Science 28 (1988) 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
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  • 172
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    Polymer Engineering and Science 28 (1988), S. 1145-1151 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The kinetics of the activated anionic polymerization of caprolactam to nylon-6 and its copolymers has been studied. Nylon-6 block copolymer and nylon-6 were prepared at various initial reaction temperatures (140°C to 165°C) by anionic polymerization in an adiabatic dewar flask. Different concentrations of poly(ethylene oxide) (PEO) in 4,4′-diphenyl methane diisocyanate (MDI)-capped PEO and 1 mole percent MDI, in a caprolactam solution, were used as the activators with the catalyst, the sodium salt of caprolactam. The kinetics of the reaction were analyzed from an adiabatic temperature rise. A new method was applied to determine the rate parameters. The activation energy, Ea, of nylon-6 and nylon-6 block copolymers were found to be 22 kcal/mole. The collision frequency factor, Ao, steadily decreased and the autocatalytic constant, Bo, decreased to a constant value of 16 with the introduction of PEO. However, it was found that the order of reaction, n, was almost a constant value at the second order for all experiments.
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  • 173
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    Polymer Engineering and Science 28 (1988), S. 1173-1181 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Chlorination of high density; polyethylene results in polymers which consist of unmodified methylene units and chlorinated methylene co-units. The effect of the concentration and distribution of chlorinated units on the solid state structure has been examined by thermal, wide angle X-ray diffraction and dynamic mechanical analysis. As the substitution becomes more random, the crystallinity, crystallite size, and crystalline perfection decrease for a given chlorine content. The chlorinated units are shown to be capable of co-crystallizing, and the concentration of chlorine in the crystalline phase increases as the distribution is made more random. Concurrently, the chlorine concentration of the amorphous phase decreases. Segregation of chlorine into the amorphous regions is most efficient when the substitution is blocky.
    Additional Material: 13 Ill.
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  • 174
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    Polymer Engineering and Science 28 (1988) 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
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  • 175
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    Polymer Engineering and Science 28 (1988), S. 1240-1247 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The reversible step growth polymerization in homogeneous continuous flow stirred tank reactors (HCSTRs), in which the condensation product (W) leaves the reactor through flashing, has been analyzed. The molecular weight distribution (MWD) of the polymer formed is governed by nonlinear coupled algebraic relations to be solved simultaneously. To find the MWD numerically a large number of these are normally solved simultaneously using a suitable iterative procedure. In this paper, these have been decoupled using the technique proposed in our earlier works (1, 2) and the MWD can now be obtained sequentially without any trial and error. This leads to considerable saving in computation time compared to methods currently used. To demonstrate the efficacy of the algorithm, the polycondensation step of the poly(ethylene terephthal-ate) (PET) formed in HCSTRs has been analyzed. The MWD, the average chain length and the polydispersity index of the polymer have been computed and it takes 0.1 CPU seconds on a DEC 1090 as opposed to the earlier method which would take seventy minutes for similar computations. The simple model of the HCSTR for the PET formation gives the effect of reactor temperature and pressure and the quantitative results have been presented in this paper.
    Additional Material: 6 Ill.
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  • 176
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    Polymer Engineering and Science 28 (1988), S. 1270-1274 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A mathematical model is presented which describes the degree of cure in a thermosetting adhesive used to bond sheet molding compound (SMC) components. The model allows computer aided optimization of the thermosetting process for any type of electromagnetic heating of the various layers of the structure (e.g. dielectric, microwave or induction), arbitrary material properties and arbitrary layer thickness. Computer simulated results are given for the particular case when the cure of the thermosetting material is initiated by its exposure to a high-power radio-frequency electric field (dielectric heating). These results indicate a strong sensitivity of the process to the thickness of the adhesive layer and the degree of coupling with the electromagnetic field. The analysis demonstrates that substantial heat losses from the relatively thin adhesive layer to the structural members of the joint by diffusive heat flow can be counterbalanced by additional electric power dissipated either in the adhesive or the structural members of the joint. Although derived for dielectric heating, those results are general, being independent of the type of electromagnetic heating employed.
    Additional Material: 5 Ill.
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  • 177
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    Polymer Engineering and Science 28 (1988), S. 1275-1275 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Linearly tapered coat hanger dies or T-dies are widely accepted. Nevertheless a newly proposed curvilinearly tapered coat hanger die has been shown to perform much better. It costs about the same as the other types of dies. This contribution is considered in terms of the recent literature.
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  • 178
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    Polymer Engineering and Science 28 (1988) 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
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  • 179
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    Polymer Engineering and Science 28 (1988), S. 1304-1312 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: We have determined the degree of stiffness of a poly(γ-benzyl α, L-glutamate) (PBLG) chain in benzyl alcohol by measuring the intrinsic viscosities of dilute Solutions with differing molecular weights. Viscoelastic properties in oscillatory shear flow have been studied and the dependence of the loss and storage moduli on temperature, composition, and frequency are reported. We have also studied the transient shear stress relaxation behavior of the PBLG gel at different temperatures and concentrations. A comparison has been made between these gels and a classical poly(dimethyl siloxane) (PDMS) network, as well as, typical glassy polymers. Shear creep and recovery measurements have been made for this system. Some extensional step strain experiments using lubricated squeezing have been investigated. Tensile experiments have been made to determine stress-strain relationship during elongation. Preliminary experiments using the impulse approach to viscoelasticity further indicate the high elastic contribution in the gel.
    Additional Material: 13 Ill.
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  • 180
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    Polymer Engineering and Science 28 (1988), S. 1342-1342 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
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  • 181
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    Polymer Engineering and Science 28 (1988), S. 1347-1354 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: It is well known that equilibrium, thermodynamic properties are governed by different functional derivatives of the thermodynamic functions of state. For example, the phase behavior of mixtures of low and/or high molar mass components is determined by the compositional derivatives of the free energy. In this contribution, the merits of the Simha-Somcynsky theory in describing and predicting the phase behavior of mixtures are considered. The influence of temperature and composition on the miscibility behavior for practically binary polymer solutions are studied. Furthermore, the important aspect of polydispersity, inherent to synthetic polymer systems will be addressed.
    Additional Material: 9 Ill.
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  • 182
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    Polymer Engineering and Science 28 (1988), S. 1572-1577 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The effect of titanate, zirconate, and zircoaluminate coupling agents on the viscosity of zirconia-polypropylene injection molding blends was investigated. The zircoaluminate did not influence viscosity while the two former additives effected a considerable reduction. The titanate coupling agent also reduced the viscosity of the polymer in the absence of ceramic powder, and was more efficient in this respect, as a flow modifier than dioctyl phthalate. A comparable effect on the ceramic suspension was obtained by adding a species similar in molecular structure to the titanate coupling agent but without coupling ability.
    Additional Material: 6 Ill.
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  • 183
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    Polymer Engineering and Science 28 (1988), S. 1581-1585 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The dielectric properties of thermoplastic and cross-linked polyethylene compounds with a low structure medium thermal carbon black are described in the frequency range between 30 and 8000 kHz as a function of frequency, temperature, and carbon black loading. Very high values of the dielectric constant were obtained for the conductive samples. The systems investigated are shown to follow percolative type models with experimental critical exponents in good agreement with the predicted values. The dielectric constant increases slowly with the carbon black concentration up to roughly the percolation concentration, then increases rapidly, and subsequently decreases at the higher black loadings. The dissipation factor-concentration curves show maximum values in the vicinity of the percolation concentration. The dielectric properties of these systems are discussed in terms of interfacial Maxwell-Wagner polarization effects.
    Additional Material: 7 Ill.
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  • 184
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    Polymer Engineering and Science 28 (1988), S. 372-376 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: This paper presents a method for analyzing the cure of multilayer circuit boards containing chemically reactive adhesive interlayers. The cure kinetics of the adhesive are first quantified by differential scanning calorimetry, using the method of Freeman and Carroll to obtain the numerical kinetic parameters. These parameters are then used in a finite-element model of the circuit board which solves the heat and species transfer equations simultaneously. It is then possible to predict the temperature and extent of reaction at any time and position within the laminate, enabling the curing program to be optimized.
    Additional Material: 6 Ill.
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  • 185
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    Polymer Engineering and Science 28 (1988), S. 403-403 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
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  • 186
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    Polymer Engineering and Science 28 (1988), S. 429-433 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A method for estimating the polymer melt extrudate temperature fluctuation in the single screw extrusion process is proposed. Predictions of the melt temperature fluctuation is feasible if the extrusion process parameters are known. The method is superior to these in the literature because it incorporates effects of the melting process on the temperature fluctuation. The method has been verified experimentally.
    Additional Material: 5 Ill.
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  • 187
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    Polymer Engineering and Science 28 (1988), S. 453-459 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: An investigation was undertaken to study the extrusion behavior of composite systems. A compound made up of approximately 50 percent ceramic particulates by volume dispersed in a high molecular weight thermoplastic polymer was characterized by measuring the shear viscosity on an Instron capillary viscometer. The experimental data indicated that the ceramic composite exhibited an apparent yield stress. As a result, an expression that was previously shown to provide flexibility for describing a yield stress at low rates of deformation could explain the viscosity of the ceramic composite. The expression was then applied to the flow analysis of both a “rod” and a “slit” die in an extrusion process, and the derived equations adequately correlated experimental volumetric flow rate us. Pressure drop data obtained on a laboratory extruder.
    Additional Material: 11 Ill.
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  • 188
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    Polymer Engineering and Science 28 (1988), S. 485-490 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A model for the molding by reactive injection of reinforced plastics for systems in which fiber glass reinforcements are placed into the molds, is proposed. It allows for the determination of processing parameters and their influence on dependent variables: conversion, temperature, and pressure. Moldability areas, where premature gelling is avoided, are defined. Operating conditions are selected to reduce cycle time, produce small load losses, and provide a fairly uniform curing stage throughout the product.
    Additional Material: 9 Ill.
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  • 189
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    Polymer Engineering and Science 28 (1988), S. 510-516 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: For linear copolymer molecules, the refractive index increment depends on the chemical composition of the molecules. However, the polydispersity in chemical composition of the sample introduces a great complexity in the data analysis in order to obtain a true molecular weight distribution. Even when the mean chemical composition does not depend on the molecular weight, a correction has to be applied when the output of an instrument depends quadratically on the refractive index Increment of the sample, such as in a light-scattering measurement. For that purpose, the light-scattering expressions are written in terms of polydispersity in chemical composition, which in turn is modeled using linear copolymerization equations. The microstructure effects, which are related to the order in which two different kinds of monomers appear along the chain, are not as yet taken into account in this approach.
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  • 190
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    Polymer Engineering and Science 28 (1988), S. 506-509 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: In this work, creep induced buckling was studied for a number of thermoplastic materials. The effect was observed by monitoring top displacements of thermoplastic bars as a function of time under static loading conditions. The recorded times to failure were averaged and correlated with the applied loads. The experiments, conducted for different materials, established an exponential dependence between the critical time and the load. The evolution of the buckling eigenvalues was modeled numerically. The simulations of eccentric columns behavior under compressive loads were coupled with the eigenvalue analyses. The correlation of the time-load predictions obtained from the numerical simulations followed the experimental results within acceptable limits. The observed phenomenon of creep induced buckling was explained by damage accumulation leading to an effective reduction of the load carrying capability.
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  • 191
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    Polymer Engineering and Science 28 (1988), S. 1042-1045 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Over the last four decades, numerous reports have appeared on the physico-chemical kinetics, especially crystallization kinetics, based on the Avrami equation, φ = exp [-Ktn] where φ is the fraction of material unchanged at time t, K is an overall rate constant and “n” is the Avrami exponent indicative of process mechanism. The usage of the Avrami equation has been limited to the determination of “n” and its temperature dependence. It is shown that the evaluation of K and the activation energy (E) using this equation is erroneous since K and E are both influenced by “n” although such would be unexpected from the Avrami equation. On the other hand, if one uses a modified expression, φ = exp[-Kt]n, then in addition to the value of “n”, correct values of K and E are obtained. This retains the original correspondence of the Avrami equation to nuclea-tion and crystal growth processes but extends its applicability to (i) correctly evaluate K and E parameters, and (ii) correctly compare transformation rates when the systems differ in their n values. Experimental data are presented to support these conclusions.
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  • 192
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    Polymer Engineering and Science 28 (1988), S. 1071-1075 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Thermosetting resin/glass cloth composites find extensive use in the packaging of electrical circuits into multi-layered circuit boards. To determine optimum processing conditions, it is necessary to understand the rheology of the resin as it cures. In this study, a squeezing flow geometry was used to determine the shear viscosity of a high performance epoxy resin during cure; Viscosity profiles were obtained during rising temperature cure. The results were compared with the complex viscosities obtained using the dynamic oscillatory parallel plate geometry. A numerical optimization algorithm was used to obtain the dual Arrhenius viscosity model parameters from the experimental viscosity data. The sensitivities of the model parameters and their effects on the predicted viscosity profiles were also determined.
    Additional Material: 8 Ill.
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  • 193
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    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 28 (1988) 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Type of Medium: Electronic Resource
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  • 194
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    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 28 (1988), S. 1107-1114 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Rheological and spiral mold flow measurements were made on blends of a chlorinated poly (vinyl chloride) (CPVC) compound and a thermotropic liquid crystalline copolyester of p-hydroxybenzoic acid/poly (ethylene terephthalate) (60/40), hereafter referred to as LCC, at 210°C. Several interesting flow phenomena have been observed. While the shape of the flow curve (i.e., G′ vs. ω; G″ vs. ω) of LCC is solidlike, those of the blends are pseudoplastic. The dynamic viscosity of the blends increases as the concentration of LCC increases. However, the shear viscosity of the blends is reduced with LCC and may be described using the relationship of additivity of fluidity. Although the melt elasticity of the blends is increased with the concentration of LCC, the extrudate swell of the blends after extrusion from a capillary is decreased. This phenomenon, however, is complicated. A Theological analysis based on an idealized runner system is used to describe the spiral flow length as a function of the Theological properties of the molten polymers and also the operating conditions. The relative improvement of the spiral flow length of the CPVC compound due to blending with LCC could be correlated with the power-law fluid model at high shear rates.
    Additional Material: 16 Ill.
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  • 195
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    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 28 (1988), S. 1355-1361 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Several authors have suggested a monotonic variation of the glass transition temperature (Tg) of miscible polymer blends as a function of composition. They usually express the results in terms of equations proposed by Couchman-Karasz, Gordon-Taylor, Fox, and several others. However, we have noticed that numerous systems exhibit a cusp when Tg is plotted as a function of composition (after correction for the presence of crystallinity when semi-crystalline polymers are involved). This cusp cannot appear when the Tg's of the two homopolymers involved are separated by less than about 52 degrees., It will be shown that this observation is quite general since it has been observed with several polyester/chlorinated polymer blends, polycaprolactone/nitrocellulose blends, and polystyrene/poly(vinylmethylether) blends; It will also be shown that this behavior is predicted in the framework of the free volume theory, with equations derived by Kovacs. According to this theory, above a critical concentration φc (relative to the plasticizer) and below a critical temperature Tc, the high-Tc, polymer no longer contributes to the free volume of the mixture whereas it does above Tc. This difference leads to a Tg-composition variation which has to be expressed by two different equations, one below Tc and the other above Tc, the cusp defining the limit of applicability of each equation.
    Additional Material: 6 Ill.
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  • 196
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    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 28 (1988), S. 1401-1404 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: There is a reciprocal relation between flow and structure in multiphase systems such as polymer blends or composites. For this reason characterization of these materials must be carried out under conditions which guarantee minimum modification of structure. Capillary rheometry is particularly ill suited as a test tool, but the small strain dynamic oscillatory method may provide the true material responses, Most frequently these are expressed as frequency, ω, dependent storage and loss shear moduli, G′ and G″, or real and imaginary viscosities, η′ = G″/ω and η″ = G′/ω. However, two other methods of data presentation seem to be more sensitive to melt structure. They are the Cole-Cole plot of η″ vs. η′ and the relaxation spectrum. Frequently, both of them indicate a binomial response. Various mechanisms leading to such behavior will be discussed.
    Additional Material: 2 Ill.
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  • 197
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    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 28 (1988), S. 1416-1426 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The morphology of compatibilized polyolef in/polyamide blends was found to be significantly dependent on the concentration of an ionomer compatibilizer (polyethylene-methacrylic acid-isobutyl acrylate terpolymer) in the blend. For a dispersed phase content of 10% by weight, a maximum reduction in phase size was observed when only 0.5% by weight of ionomer was added to the blend, A more significant reduction of the dispersed phase size was observed when the minor phase was nylon, due to interactions which exist between the ionomer and the polyamide. These interactions have been confirmed by Fourier transform infrared spectroscopy. At high concentrations of the ionomer, flocculation of the nylon dispersed phase was observed. In comparison to one-step mixing, blends prepared by two-step or batch mixing were characterized by a smaller dispersed phase when nylon was the matrix, and a larger particle size when nylon was the minor phase. The results observed are explained in terms of a speculative model of the interactions occurring across the nylon-polvolefin interface.
    Additional Material: 14 Ill.
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  • 198
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    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 28 (1988), S. 1445-1449 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: It is shown that polyethylene and crossllnked polyethylene resins used for cable applications contain an antioxidant synergist in addition to an antioxidant. Their nature and content have been determined by a combination of ultraviolet and Fourier transform infrared spectroscopy and neutron activation analysis measurements. The results thus obtained suggest that part of the antioxidant compound is grafted to polymer chains during crosslinking.
    Additional Material: 7 Ill.
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  • 199
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    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 28 (1988), S. 1455-1461 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The effect of Cryogenically Ground Rubber (CGR) from old tires on some mechanical properties of an unsaturated polyester resin is presented. A delay in the free radical cure reaction of the unsaturated polyester resin was observed upon the addition of ground rubber. This delay in the cure reaction could be overcome with the further addition of the free radical initiator. The particle size, surface chemistry, and the chemical composition of the rubber had an effect on the cure and on the final properties of the rubber-filled composites. It was also found that the rubber particles decreased the tensile, flexural, and storage shear modulus of the unsaturated polyester. Composites made from silane-treated ground rubber showed better mechanical properties than composites made from untreated CGR. Finally, the particle size of the ground rubber was apparently too large to produce a toughening effect on the filled materials.
    Additional Material: 5 Ill.
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  • 200
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    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 28 (1988), S. 1517-1526 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: We describe the computer-aided engineering analysis of a linearly tapered coat-hanger die in this paper. The general governing equation for flow distribution inside the die was derived first. On the basis of this equation, we have developed the design formula for a die to deliver uniform flow. In addition, we have also examined the variations of lateral flow uniformities and residence time distributions of polymeric liquids under several different design and operating conditions: (1) using manifolds with non-circular cross-sections, (2) adjusting production widths, (3) delivering fluids with different viscosities, and (4) enlarging manifolds for practical production considerations.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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