Library

Your email was sent successfully. Check your inbox.

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

Proceed reservation?

Export
Filter
  • 1980-1984  (3,638)
  • 1980  (3,638)
  • Polymer and Materials Science  (2,926)
  • Chemical Engineering  (478)
  • Engineering  (233)
  • Nuclear reactions
Material
Years
  • 1980-1984  (3,638)
Year
  • 101
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemie Ingenieur Technik - CIT 52 (1980), S. 249-251 
    ISSN: 0009-286X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 102
    ISSN: 0009-286X
    Keywords: Rühren ; Reaktor ; Dispergieren ; Leistungscharakteristik ; Suspendiercharakteristik ; Überflutungscharakteristik ; gerührte ; begaste Suspensionsreaktoren ; Leistungsbedarf ; Dreiphasen-system ; Dreiphasenreaktor ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 103
    ISSN: 0009-286X
    Keywords: Airlift-Schlaufenreaktor ; Gasgehalt ; Stoffübergang ; Längsvermischung ; Mischzeit ; Umlaufgeschwindigkeit ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 104
    ISSN: 0009-286X
    Keywords: Begasen ; Belüften ; selbstansaugender Rührer ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 105
    ISSN: 0009-286X
    Keywords: Schlammentwässerung ; Schlammcharakterisierung ; Flockungsmittel ; Flockungsreaktion ; Flockungsreaktoren ; Entwässerungsmaschinen ; Siebtrommeln ; Kammerfilterpressen ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 106
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemie Ingenieur Technik - CIT 52 (1980), S. 451-453 
    ISSN: 0009-286X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 107
    ISSN: 0009-286X
    Keywords: Rauchgasentschwefelung ; NOx-Reduktion ; Adsorption ; heterogene Katalyse ; Aktivkoks ; Schwefeldioxid ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 108
    ISSN: 0009-286X
    Keywords: Trennkurve ; Differenzenformel ; Fehleranalyse ; Meßwertausgleich ; Fehlerabschätzung ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 109
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemie Ingenieur Technik - CIT 52 (1980), S. 472-473 
    ISSN: 0009-286X
    Keywords: Sicherheit ; Explosionsschutz ; Sauerstoff ; Inertgas ; Sp¨lung ; Behälter ; Druckwechsel ; Durchströmung ; Schiittgüt ; Eintrag ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 110
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemie Ingenieur Technik - CIT 52 (1980), S. 504-515 
    ISSN: 0009-286X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Methanization of carbon monoxide-rich gases for energy-transport. The partners of the NFE project (Nukleare Fernenergie, Remote nuclear energy) - Kernforschungsanlage Jülich GmbH (Germany) and Rheinische Braunkohlenwerke AG, Köln (Germany) - in collaboration with Haldor Topsøe A/S, Copenhagen (Denmark), have investigated various problems of the methanization of synthesis gases rich in carbon monoxide. Preliminary results obtained from trial operations with the pilot-scale methanization plant ADAM I at KFR Jülich and from the catalyst-development project at Haldor Topsøe A/S are reported. A detailed account is given of the catalyst investigations carried out on the Haldor Topsøe pilot plant for the further development of the TREMP process for SNG manufacture and of the complementary catalyst investigation in the NFE project at the Union Rheinische Braunkohlen Kraftstoff AG and the Kernforschungsanlage Jülich GmbH for the optimization of the methanization process in the remote energy system EVA-ADAM. In the pilot plant ADAM I, a three-stage methanization process with product gas recycling and maximum temperature of 600 °C utilizing synthesis gas from methane vapour reforming (EVA) has been demonstrated for the first time. In further experiments to be carried out with ADAM I the influence of operating irregularities on the behaviour of the methanization plant and the dynamics of the remote energy system will be investigated, data for the preparation of mathematical models collected, new components tested, and the process of methanization optimized.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 111
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemie Ingenieur Technik - CIT 52 (1980), S. 520-522 
    ISSN: 0009-286X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 112
    ISSN: 0009-286X
    Keywords: Chargenkristallisation ; Kühlungskristallisation ; Leitrohr-Rührwerkskristallisator ; Korngrößenverteilung ; mittlerer Korndurchmesser ; Kornform ; sekundäre Keimbildung ; Maßstabsvergrößerung ; Kaliumchlorid ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 113
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemie Ingenieur Technik - CIT 52 (1980), S. 542-543 
    ISSN: 0009-286X
    Keywords: Vollmantelschneckenzentrifuge ; Entfeuchtung ; Restfeuchte ; Dimensionierung ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 114
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemie Ingenieur Technik - CIT 52 (1980) 
    ISSN: 0009-286X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 115
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemie Ingenieur Technik - CIT 52 (1980), S. 562-570 
    ISSN: 0009-286X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Fractional crystallization. The operations of fractional crystallization, comprising at least a single crystallizing and remelting (redissolution) step, differ from each other in the number of the realized theoretical stages and the method of separating the crystallisate and residual melt or mother liquor. Fractional crystallization from solutions resemble liquid-liquid extraction, but fractional crystallization from melts is similar to rectification. There is a choice between operations with a series of temperature-controlled vessels and counter-current operations. Many fractional crystallizers are purifiers for high qualities; crystals generally exist only within them apparatus.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 116
    ISSN: 0009-286X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 117
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemie Ingenieur Technik - CIT 52 (1980), S. 594-595 
    ISSN: 0009-286X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 118
    ISSN: 0009-286X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 119
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemie Ingenieur Technik - CIT 52 (1980), S. 762-763 
    ISSN: 0009-286X
    Keywords: Brine electrolysis ; undivided electrochemical reactors ; anode-cathode ratios ; hypochlorite ; roughness ; electrodes ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 120
    ISSN: 0009-286X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 121
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemie Ingenieur Technik - CIT 52 (1980), S. 794-802 
    ISSN: 0009-286X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 122
    ISSN: 0009-286X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 123
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemie Ingenieur Technik - CIT 52 (1980), S. 816-818 
    ISSN: 0009-286X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 124
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemie Ingenieur Technik - CIT 52 (1980), S. 830-830 
    ISSN: 0009-286X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 125
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemie Ingenieur Technik - CIT 52 (1980), S. 838-839 
    ISSN: 0009-286X
    Keywords: Blasensäule ; Dispersionsmodell ; Flüssigphase-Durchmischung ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 126
    ISSN: 0009-286X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Improved cost factor estimation with quantity and man-hour ratios. Present-day cost estimation on a multi-currency basis is becoming more and more complex due to the wild and frequent fluctuations of exchange rates and different inflationary trends in various countries. The preparation of comparatively accurate preliminary cost estimates, based on world-wide procurement, overseas construction and engineering, became a major problem for companies like badger with international activities. To maintain an acceptable degree of accuracy, the traditional method of cost factor estimation has to be supplemented with a quantity and man-hour ratio method. Basically, costs are related to quantities; therefore cost ratios can be converted into quantity ratios. Man-hour ratios originate from the existing relationship between quantities, material costs, and field man-hours to install these quantities. In this article the value of the Quantity Ratio Method as a tool in these unstable times will be stressed, as well as the added advantages it offers with regard to better cost control and communication.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 127
    ISSN: 0009-286X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 128
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Poly[2-(methylsulfinyl)ethyl acrylate] (1) was synthesized as well as derivatives 14C-labelled in side groups (6) or 14C-labelled in the main chain (11). Polymer 11 with the 14C-labelled main chain was fractionated by precipitation. The η-M-relation determined by measurements of unlabelled polymers in the ultracentrifuge for comparison was used to establish the viscosimetrically determined molecular weights of the labelled fractions. After intravenous application of aqueous solutions of the polymer in rats the excretion rate up to 72 h after treatment was ascertained to ca. 50%; the concentration in the blood serum was found to be strikingly high. A tendency to reinforced storage in organs of high phagocytose activity by growing molecular weight was observed. The tumor affinity was  -  if at all  -  low.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 129
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 277-288 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The low-frequency viscoelastic behaviour of three stereoregular samples of poly(ethyl methacrylate) (PEMA) in the main transition region was investigated. The main effect of tacticity in the transition from the syndiotactic sample to the isotactic one consists in a shift of the main transition region (or of the glass transition temperatures, Tg) to lower temperatures by ≈ 70 K. The temperature dependence of the shift factor of all samples could not be adequately described by the single Williams-Landel-Ferry (WLF) equation within the whole range of temperatures; in the range T〉Tg+60K, isotactic PEMA exhibited the largest departures from the WLF equation. In all cases, departures from the WLF equation could be quantitatively described in terms of the temperature dependence of the Andreade coefficient β. The temperature dependence of the Andreade compliance, JA, was also most pronounced for the isotactic sample. Vertical correction of the complex modulus G*, with WLF horizontal shifts preserved, led to the lowest activation energy ΔH for the isotactic sample, which means the highest magnitude of secondary relaxation mechanism in this sample. The birefringence measurement showed that the molecular nature of the deformational birefringence is independent of the tacticity of the sample and does not vary in the range Tg+25K〈T〈Tg+100K. In all the characteristics mentioned here, parameters of a conventional sample obtained by radical polymerization approached those of the syndiotactic sample.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 130
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The synthesis of some series of oligo(oxytetramethylene oxyterephthaloyl) [oligo(butylene terephthalate)s] with different but well-defined end groups is described. The separation of artificial mixtures of the oligomers by high pressure liquid chromatography was studied under various elution and column conditions, and thus, the purity of the individual oligomers was demonstrated. The equilibrium melting point Tm0 = 236 ± 4°C and the corresponding heat of melting ΔHm0 = 28,7 kJ·mol-1 of poly(butylene terephthalate) was determined from the analysis of the melting behaviour of the oligomers as depending on the degree of polymerization and the structure of the end groups.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 131
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 333-340 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Several potentially thermostable polyamides were prepared. 2,2′-Diiodobiphenyl-4,4′-dicarboxylic acid and its diacid chloride 1 were synthesized. The latter was condensed with several amines, e.g., aniline, p-toluidine, p-chloroaniline, and 2-aminopyridine, to prepare model compounds of polyamides testing the reactivity of the diacid dichloride 1 towards various amines, and to compare their spectra with those of the polymers. The polyamides themselves were prepared by solution and melt condensation of diacid chloride 1 with the following diamines: p-phenylenediamine, m-phenylenediamine, 2,6-diaminotoluene, benzidine, bis(4-aminophenyl)-methane, 4,4′-diaminobiphenyl sulfone, and 3,3′-diaminobenzophenone. The solubility of the polyamides in different solvents and their inherent viscosities were also measured. The values of the inherent viscosity were in the range of 0,1-1,9. The UV, IR, and 1H NMR spectra of the prepared polyamides were recorded. The melting points of the polymers were found to be higher than 360°C and the thermogravimetric curves showed that the polymers are stable up to 400°C in air.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 132
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 373-382 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A series of pure ethylene polymerizations performed to maximum pressures of 2,5 kbar and temperatures up to 250°C is discussed. The rate data which are obtained via quantitative infrared and near infrared spectroscopy closely fit to an overall polymerization rate law of the order 2,5 ± 0,2 in the ethylene concentration. The overall activation energy is determined to be 136,3 ± 6 kJ/mol. For the initiation reaction an activation energy of 209,8 ± 12 kJ/mol is derived. This fairly large value establishes that in dense high purity ethylene a thermally initiated (spontaneous) reaction to high molecular weight material occurs.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 133
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 383-397 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: NMR chemical shifts of the methoxyl and α-methyl protons in the alternating methyl methacrylate-styrene copolymer are calculated by taking into account the contributions of the diamagnetic shielding and the magnetic anisotropy effect of the benzene rings in styrene units. The conformational probabilities of the copolymer chain are calculated according to Flory's matrix method. It is deduced from the calculation that NMR should occur at higher field for the methoxyl and at lower field for the α-methyl protons of the methyl methacrylate unit in meso configuration with an adjacent styrene unit (regarding the methoxycarbonyl and phenyl groups) than for the corresponding protons in the unit of racemic configuration. Further, the differences between the chemical shifts for these protons in meso and racemic dyads are nearly equivalent to the differences in chemical shifts between two adjacent peaks of the observed triplet spectra. This result indicates that the spectral assignment based on a theoretical calculation is quite consistent with the one made by a conventional simulation method: from the lower magnetic field, peaks of cosyndiotactic, coheterotactic, and coisotactic triads appear in this order for the methoxyl protons and in the opposite order for the α-methyl protons. Magnetic anisotropy effect contributes to these tacticity-dependent chemical shifts to a far greater extent than diamagnetic shielding. The variation of the chemical shifts due to measuring temperature, probability of isotactic addition, and interactions between groups more than five bonds apart is also discussed.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 134
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 823-838 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The viscosity of aqueous polyacrylamide solutions does not remain constant. During a period of many weeks it decreases by as much as 30%. Simultaneously a loss of flocculation activity occurs. This unusual behaviour  -  also called ageing or solution instability  -  is examined. Viscosity and light scattering investigations were made. The viscosity was also determined by addition of substances which influence hydrogen bonds. It could be demonstrated, that in high molecular weight polyacrylamide hydrogen bonds are effective. Light scattering measurements result in curved angular dependence of scattered light, which must be regarded as real and specific for the high molecular weight polyacrylamides in water. The Zimm plot for polyacrylamide in ethylene glycol was undistorted. The refractive index increment decreases with time during the investigations. From the Zimm plots it follows, that the radius of gyration decreases with time. The molecular weight however remains constant. Based on the experimental results a mechanism is assumed with a long-term conformational change of the macromolecules. The orientated segments  -  stabilized by hydrogen bonds  -  are slowly destroyed by occupation of “active sites” by water molecules. Chain degradation as well as disentanglement could be excluded. A molecular interpretation is given.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 135
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Among the methods to introduce functional groups in macromolecular compounds, the initiation of free radical polymerization by functional peroxyesters was investigated. m- and p-tert-butyldioxycarbonylbenzoic acids (3 and 8) were synthetized and their properties were studied. Differential scanning enthalpimetric study of the thermolysis kinetics of 3 and 8 led to the conclusion that these compounds are a little more stable than O,O-tert-butyl hydrogen monoperoxyphthalate (1). Thus, they could be applied under similar conditions. Solution and bulk polymerizations of styrene initiated by 3 or 8 were found to be efficient methods to obtain polystyrene substituted by carboxylic functions.
    Additional Material: 5 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 136
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Modified polystyrenes were obtained by free radical polymerization of styrene using the macroinitiators α-tert-butyldioxyterephthaloyl(or phthaloyl)-ωtert-butyldioxyterephthaloyl(or phthaloyl)poly(oxyethylene) (3 and 4), which were synthetized. To examine the stability of such compounds, thermolysis kinetics of model compounds, OO-tert-butyl O-methyl monoperoxyphthalate (6) and terephthalate (7) were studied by differential scanning enthalpimetry. Suspension polymerization of styrene applying the industrial method, showed that the macroinitiator is able to initiate the process. A polystyrene containing up to 4% by weight oxyethylene units was obtained.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 137
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: 1H NMR spectra of alternating copolymers of methyl acrylate with styrene, methyl acrylate with α-methylstyrene, and methyl methacrylate with α-methylstyrene show triplet splittings at the methoxyl protons regions, which apparently reflect the cotacticity of triad sequences having a (meth)acrylate unit in the center. The two intervals between two neighboring peaks of the triplet are nearly equivalent for each alternating copolymer, whereas the absolute value of the splitting width is significantly different from one alternating copolymer to another. A theoretical interpretation is given for this observation by calculating the chemical shifts of the methoxyl protons in combination with a conformational analysis of the copolymers. The chemical shift of the protons in meso or racemic type dyad sequence is assigned by averaging the shieldings over all the preferred conformations for the dyad and is accumulated to give the shifts in triad sequences: iso = meso + meso, hetero = meso + racemic, syndio = racemic + racemic. The cotacticity-dependent splittings thus calculated are quantitatively in accordance with the observed spectra and discussed in terms of conformational variation of the copolymers depending on the presence of α-methyl group(s) in neither, either, or both of the monomeric unit(s).
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 138
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 1051-1058 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Chlorination under mild conditions of suspensions of polyethylene single crystals demonstrated that a selective attack on the fold surface takes place. Two polyethylene molecular weight fractions (Mn = 47000 and Mn = 150 000) were used and single crystals were grown isothermally from p-xylene at 88°C. The chlorine content was changed from 4 wt.-% to 30 wt.-% and to this level no evidence for crystal attack and loss of crystallinity was found. The melting temperatures of chlorinated single crystals decrease with increasing chlorination up to about 15 wt.-% chlorine content and then stay constant for higher chlorine contents. Moreover, the heat of melting of the chlorinated single crystals is constant and is independent of the chlorine content up to 25 wt.-%. These results are compared with those of samples of chlorinated polyethylene recrystallized from solution and from the melt.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 139
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 1143-1157 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The crystallization of cross-linked cis-1,4-polybutadiene, stretched at room temperature, is investigated by wide and small angle X-ray diffraction techniques, at temperatures ranging from -40°C to the melting point, Tm, and for extension ratios, λ, from 1 to 7,7. The experimental conditions adopted should approximate thermodynamic equilibrium. All the experimental findings, namely, crystallinity, preferred orientation of the crystalline and amorphous fractions, unit-cell dimensions and others, are consistent with the formation of two types of crystals: one depending mainly on stretching, the other on temperature. The former is characterized by extended chain crystals with Tm higher than the isotropic melting point (Tm0 = -3°C); the latter by a lamellar (bulk-like) morphology which is stable only below Tm0. A slight increase of Tm occurs for λ 〈 3, when the axes of the crystallized chains are tilted with respect to the strain direction; only when untilted crystals are formed (λ 〉 3) a remarkable increase of Tm is observed as a function of λ. As a qualitative interpretation, the two-fold crystallization mechanism is based on non-uniform extensibility of the segments included between adjacent junctions of the network.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 140
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 1459-1467 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: N,N′-diethylpseudoisocyanine chloride (PIC) forms compounds with various vinyl poly+ and DNA, but the shapes of the spectra of the dye-polyanion compounds depend on the nature of the polyanions. PIC forms compounds with 1:1 polyanion/dye stoichiometries with DNA (native and denatured), polymethacrylate and poly(styrenesulfonate); and the spectra of these compounds do not show any pronounced metachromasia or red-shifted J-band. Polyacrylate and poly(vinyl sulfate) form compounds with polyanion/dye stoichiometry of 2:1, and give spectra with extremely sharp and red-shifted J-band. This is the first report on the relation between the polyanion/PIC stoichiometry and the depiction of the J-band of the resulting compound.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 141
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 1495-1504 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A new fluorene containing polymer, poly[2-(2-fluorenyl)-1,3-dioxan-4,6-diylmethylene] (3 or 4), and the corresponding model compound, 2-fluorenecarbaldehydetrimethyleneacetal (6) were synthesized. The fluorescence spectroscopy of the polymer in dilute solution indicates the formation of an intramolecular excimer. Charge-transfer complex formation with tetracyanoethylene (TCNE), 2,5-cyclohexadien-1,4-diylidenedimalonodinitrile (TCNQ), and 2,4,5,7-tetranitro-9-fluorenone (TENF) was studied by means of absorption spectroscopy.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 142
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 2259-2266 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Allyl vinyl ether can be polymerized to highly isotactic polymer with SbCl5 in toluene at ca. -10°C. The stereospecificity is not significantly lower than that of polymer made at ca. -75°C; The reproducibility of the process is greatly improved at the higher temperature. BF3.O(C2H5)2 proved to be an ineffective initiator, in contrast with literature data. NMR analysis, previously published for diads only from NMR data, was performed (1H and 13C) for triads as well, and partly for hexads. No evidence for stereocontrol other than the relationship between active chain end HC⊕OAllyl and incoming monomer can be inferred1cf. Part 2 of this series10.. A simple mechanism, featuring association between incoming monomer and counterion, invoking only steric hindrance is proposed as an explanation of these findings.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 143
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 2293-2303 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Formation and behaviour of radiation induced free radicals in statistical copolymers from vinyl hydrosulfide and styrene (1:1, 1:4, and 1:10) were investigated by means of ESR spectroscopy. The corresponding homopolymers were also included in these studies. After γ-irradiation of the copolymers at 77 K and subsequent annealing to 293 K it was possible to detect thio radicals. Their relative yields were found to increase with increasing styrene content. Investigations regarding the thermal behaviour of the radiation induced radicals in the copolymers allowed the assumption of two mechanisms responsible for the formation of the thio radicals: First, the formation takes place via ion radicals located at the mercapto groups at 77K. In the copolymers the stability of the thio radicals is favoured by steric hindrance through the benzene rings thus reducing the formation of disulfide bridges as termination reaction. Secondly, the formation of the thio radicals is caused by a hydrogen transfer from the mercapto groups to the benzyl radicals and/or cyclohexadienyl radicals of styrene units.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 144
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 2325-2333 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Template polycondensations of di-p-nitrophenyl methylsuccinate derivatives of thymine (1) and theophylline (2) with piperazine and 4-aminomethylbenzylamine (4-ABA) were carried out in pyridine/methylene chloride and in DMF solutions. Polystyrenes containing adenine as a side group in various contents were used as template in this polycondensation. The polycondensation reactions of active ester 1 with diamines were effectively accelerated by the presence of the template in both solvents. On the other hand, the polycondensation reactions of active ester 2 with diamines were scarcely affected by the template under the same conditions. The maximum acceleration effect was observed in the presence of templates in which the adenine content is about 54% for the polycondensation of 1 with piperazine and about 25% for that with 4-ABA, respectively.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 145
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 2315-2323 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Poly(5,6-dihydro-2H-pyran-2,6-diyloxymethylene) (6), a new polyacetal having a dihydropyran ring in its repeating unit was prepared by selective ring-opening polymerization of 6,8-dioxabicyclo[3.2.1]oct-2-ene (5) at temperatures between -60 and -90°C in dilute methylene chloride or toluene solutions using boron trifluoride etherate as initiator. The resulting polymers, having a number average molecular weight up to 1,5 · 104, melted at 110 - 130°C and decomposed at ≈ 170°C in air. The isotactic dyad content of the polymers, estimated by 13C NMR spectroscopy, was found to be in the range of 70 to 77 mole-%, somewhat lower than that of its saturated analogue, poly(tetrahydropyran-2,6-diyloxymethylene), (2). The preferred formation of the isotactic sequence along the polymer chain is rationalized in terms of the enantiomer selection by the growing chain end control mechanism as previously proposed for the polymerization of 6,8-dioxabicyclo[3.2.1]octane, (1).
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 146
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 2409-2411 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Provided that in molecular weight determinations by vapor pressure osmometry (VPO) the relationship between M and the measured quantity (δV/c)c=0 obeys a calibration function of the type (δV/c)c=0 = KM-a, the kind of molecular weight average M̄VPO delivered by this method is derived. The deviation of M̄VPO from the true number average molecular weight M̄n is estimated from its dependence on the polydispersity and the exponent a of the calibration function.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 147
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Acrylamide (AAm), methacrylamide (MAm), N-methylacrylamide (NMAAm) and N-methylmethacrylamide (NMMAm) were found to yield long-lived propagating polymer radicals in the photo-sensitized polymerizations in 1,4-dioxane or benzene. The concentration of poly(NMAAm) radicals reached 1.10-3 mol/l. Some post-effect was observed at room temperature in the photo-sensitized polymerization of AAm with di-tert-butyl peroxide in 1,4-dioxane, while no post-polymerization proceeded at room temperature in the polymerization of NMMAm in benzene. The reactions of poly(NMAAm) and poly(NMMAm) radicals with various vinyl monomers were found to produce long-lived propagating polymer radicals of the second monomers at room temperature. Polymer radicals of non-homopolymerizable monomers such as α-methylstyrene and 1,1-diphenylethylene were easily formed in such a block-copolymerization matrix. The formation of the propagating polymer radicals of the vinyl monomers was investigated by means of ESR spectroscopy.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 148
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Molecular weights of Trogamid T® were determined by ultracentrifugation, light-scattering, osmometry and viscometry, molecular weight distributions by gel permeation chromatography (GPC) and five different fractionation methods. The separation efficiency of GPC with N,N-dimethylformamide as solvent was tested with three different types of gels, crosslinked polystyrene, porous glass and crosslinked poly(vinyl acetate), the last one yielding the best results. Solution fractionations show better results than precipitation methods. All fractionations gave far too small apparent non-uniformities. After correction according to the non-uniformities of the fractions the results corresponded to those of the other methods. All methods resulted in U = M̄w/M̄n - 1 = 0,7 for the technical product Trogamid T®. The discrepancy to U = 1 of a Schulz-Flory distribution can be explained by the influence of the path of reaction.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 149
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 111-124 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Interfacial condensation polymerization of bischloroformates of bisphenol A with bisphenol A results in the formation of cyclic aromatic polycarbonates of high molecular weight. Products made by this technique show a significant reduction (up to 95%) in their end group content. Also, in comparison to molecular weights determined by light scattering, these products show markedly lower molecular weights by solution viscocity measurements and by applying the Mark-Houwink equation for linear polycarbonates. The existence of high molecular weight cyclic polycarbonates is confirmed by a controlled saponification reaction using piperidine as a basic compound. The saponification reaction causes nearly no change in the number average molecular weight of the polymer and causes an increase in the number of end groups of up to 2 end groups per molecule. The observed increase in the intrinsic viscosity data is similar to what would be expected from linear polycarbonates. It is shown that cyclic polycarbonates with molecular weights exceeding 100 000 are easily obtained.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 150
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The spontaneous thermal polymerization of methyl methacrylate (MMA) is accompanied by the production of serveral oligomers among which a linear unsaturated dimer H-1 (dimethyl 1-hexene-2,5-dicarboxylate) is predominant. The reaction kinetics of this dimer formation was investigated in bulk and in solution. The temperature dependence of the second order dimerization constant was determined as \documentclass{article}\pagestyle{empty}\begin{document}$$ \log _{\rm e} k_{{\rm H} - 1} = 13,11 - \frac{{107,2{\rm }{{{\rm kJ}} \mathord{\left/ {\vphantom {{{\rm kJ}} {{\rm mol}}}} \right. \kern-\nulldelimiterspace} {{\rm mol}}}}}{{RT}} $$\end{document} Reaction mechanisms for the thermal dimer formation of MMA are discussed.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 151
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 125-130 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The preparations of 2,4-bis(4-bromophenyl)pentane (1b) and 2,4,6-tris(4-bromophenyl)heptane (2b) are described. The study of the different isomers of 1b and 2b by 13C NMR allows a comparison of the various configurational sequences of these compounds in terms of their chemical shifts. Methyl, methylene, and aromatic C1 carbons of 1b and 2b could be deduced from the values obtained from corresponding polystyrene model compounds by a mere translation. From the aromatic C1 chemical shifts it was possible to propose an assignment of the corresponding triads of poly(4-bromostyrene).
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 152
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: 13C NMR has been used to study the helix-coil transition induced in polypeptides by trifluoroacetic acid. An attempt is made to separate the influences of conformational change and direct solvent interaction. For poly(γ-methyl-L-glutamate), interactions between trifluoroacetic acid and the ester group of the side chain occur in the helical region. Poly(L-norvaline) and poly(L-norleucine) are in the form of “partially distorted helical conformation”. Conformational change and the interaction between trifluoroacetic acid and the peptide group which accompany the helix-coil transition, affect the chemical shift difference up to Cδ or Cβ of poly(L-norvaline) and poly(L-norleucine), On the contrary, in the case of polyglutamates and polyaspartate, these effects are minor for the carbons in the ester portion. The chemical shift differences of these polypeptides can be well interpreted qualitatively by the results for some butyrates, poly(L-norvaline), and poly(L-norleucine).
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 153
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 177-191 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The origin of the chemical shift differences of carbons in polypeptides which accompany the helix-coil transition has been investigated by using oligopeptides, benzyloxycarbonyl-γ-ethyl-L-glutamyl-diethyl-L-glutamate and benzyloxycarbonyl-di-(γ-ethyl-L-glutamyl)-diethyl-L-glutamate, as models of the backbone of polypeptides. Structures of aggregates in deuterated chloroform were proposed for these oligopeptides on the basis of concentration dependence and temperature dependence of the chemical shifts of protons and carbons, and spin-lattice relaxation times. Antiparallel and/or parallel “in-register” structures for extended forms and “out-of-register” network of extended forms are coexisting in deuterated chloroform solution for these oligopeptides. From the shift for the carbons of the oligopeptides induced by organic acids, it was in ferred that down-field shifts are induced at α and amide carbons in polypeptides by organic acids. By comparing the induced shift of the carbons in the peptides with the chemical shift differences of the carbons in polypeptides which accompany the helix-coil transitions, it was found that the conformational changes play a predominant role in the origin of the chemical shift differences of the carbons in polypeptides which accompany the helix-coil transitions, it was found that the conformational changes play a predominnant role in the orgin of the chemical shift differences of amide, α, β, and γ carbons in polypeptides.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 154
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 193-199 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In order to clarify the arrangement of sulfated poly(vinyl alcohol) (PVS) chains about the α-helical poly(L-lysine) (PLL) chain in the previously reported complexes of PLL/46 mole-% sulfated poly(vinyl alcohol) (PVS-46) and PLL/PVS-95, induced circular dichroism was studied on PLL/PVS/acridine orange (AO) complexes in acidic aqueous solution. A positive ellipticity, [θ], of ca. 3 400 deg·cm2·dmol-1 at 465 am and small negative values of [θ] at 435 and 510 nm indicated a right-handed super helical arrangement of AO molecules about the right-handed α-helix of PLL, where PVS chains were intercalated. The amount of AO molecules responsible for the induced CD was estimated as low as a few mole-%. Taking into consideration the arrangement of ε-amino groups of the right-handed α-helical PLL and the distance among the neighboring ε-amino groups on the radial projection of the helix, the PVS chain segments could be arranged both in the right-handed and in the left-handed superhelices about the right-handed α-helix of PLL. In cases of the PLL/PVS-25/AO and PLL/PVS-30/AO complexes, no induced CD and a quite weak CD were obtained, resp., being consistent with random coil conformation of PLL in the PLL/PVS-25 and PLL/PVS-30 complexes mentioned previously.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 155
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 227-240 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Using a set of laboratory poly(acrylamide) samples in the molecular weight region M̄w = 5.105 to M̄w = 6.106 the following relations have been established, the polymer concentration c given in g/cm3: \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{*{20}c} {[\eta ] = 4,9 \cdot 10^{ - 3} \bar M_{\rm w}^{{\rm 0,8}} } \hfill & {\rm,} \hfill & {{\rm solvent: H}_{\rm 2} {\rm O, temp}{\rm .: 298 K}} \hfill \\ {[\eta ] = 7,19 \cdot 10^{ - 3} \bar M_{\rm w}^{{\rm 0,77}} } \hfill & {\rm,} \hfill & {{\rm solvent: 0,5 M aqueous NaCl, temp}{\rm .: 298 K}} \hfill \\ {[\eta ] = 1,36 \cdot 10^{ - 1} \bar M_{\rm w}^{{\rm 0,54}} } \hfill & {\rm,} \hfill & {{\rm solvent: ethylene glycol, temp}{\rm .: 298 K}} \hfill \\ {s_0 = 0,9 \cdot 10^{ - 1} \bar M_{\rm w}^{{\rm 0,32}} } \hfill & {\rm,} \hfill & {{\rm solvent: 0,5 M aqueous NaCl, temp}{\rm .: 293 K}} \hfill \\ \end{array} $$\end{document}([η], intrinsic viscosity; s0, sedimentation constant) Mainly based on light scattering experiments a more detailed description on molecular dimensions and solution structure of PAAm/H2O and PAAm/ethylene glycol systems is given. In both systems the relation a = 3v - 1 (a and v being the exponents of the intrinsic viscosity  -  and root-means-square end-to-end distance  -  molecular weight functions) holds.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 156
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 255-260 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The effect of UV light (λ 〉 300 nm) on the system styrene/maleic anhydride/solvent (acetone or chloroform) in the presence and/or absence of the alternating styrene/maleic anhydride copolymer was studied by the ESR method at -196°C. It was found that the concentration of paramagnetic species increased with the time of irradiation. The intensity of the ESR spectra at -196°C did not change when the light was cut off. By analysis of the ESR spectra of the systems studied the methyl (aH = 2,3 mT), dichloromethyl (aH = 1,66 mT), and acetyl (aH = 0,52 mT) radicals as well as the radicals A and D (aHα = 2,25 mT, aHβ = 3,19 mT) and (aHβ = 1,1 mT), respectively, were identified.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 157
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 267-276 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Products with 〉90% of 1,4-cis-units in the grafted chains are obtained by employing suitable concentrations of cobalt complexes as an initiator component in the grafting of butadiene onto chlorinated polycyclopentadiene. Grafting efficiencies 〉90% can be achieved. In contrast to grafting without using cobalt complexes the reaction rate is faster. Suitable solvents are chlorobenzene, 1,2-dichloroethane, or dichloromethane. Grafting efficiency, degree of grafting, and the molecular weights of the grafted chains are obtained by selective extraction of the grafts with pentane. The results suggest a cationic-coordinative mechanism, in most cases accompanied by a “pure” cationic grafting.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 158
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 367-372 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Copolymers of methacrylaldehyde with hydrophilic monomers  -  2-hydroxyethyl methacrylate, 5-hydroxy-3-oxapentyl methacrylate, 8-hydroxy-3,6-dioxaoctyl methacrylate, N-ethylmethacrylamide, N,N-diethylacrylamide, and N,N-diethylmethacrylamide  -  were prepared by solution polymerization in N,N-dimethylformamide initiated with 2,2′-azodiisobutyronitrile. In the copolymer of methacrylaldehyde (1) with 2-hydroxyethyl methacrylate (2) (r1 = 0,77, r2 = 0,36) and in the copolymer of methacrylaldehyde with N,N-diethylacrylamide (r1 = 3,79, r2 = 0,14) the content of CH=O groups corresponds to that ot methacrylaldehyde units in the triads comonomer  -  methacrylaldehyde  -  comonomer; in the copolymer of methacrylaldehyde with N-ethylmethacrylamide (r1 = 4,07, r2 = 0,14) both comonomers react with each other and the content of CH=O groups is very low, while in the copolymer of methacrylaldehyde with 5-hydroxy-3-oxapentyl methacrylate (r1 = 1,48, r2 = 0,34) the majority of methacrylaldehyde units contain an unreacted CH=O group.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 159
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 399-407 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Steady shear viscosities were measured over a range of shear rates from lower to upper-Newtonian flow region for solutions of polystyrene in the high-viscosity solvent tricresyl phosphate at three different temperatures. The influence of solvent viscosity on the non-Newtonian flow property was studied and compared with the results obtained previously by use of a lowviscosity solvent with similar solvent power for polystyrene as tricresyl phosphate. For the moderately concentrated solutions, the non-Newtonian viscosity could be explained by Graessley's entanglement viscosity theory modified by a frictional viscosity. The result shows that only the frictional viscosity is affected by variation of solvent viscosity. As the entanglement viscosity decreases with increasing shear rate and is practically masked by the shear independent frictional viscosity, the flow appears as to be upper-Newtonian in spite of the difference in solvent viscosity. The lower critical concentration for entanglement was determined on the basis of a lower limit for the applicability of the modified Graessley theory. The values of the critical concentrations are independent of the magnitude of solvent viscosities.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 160
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The viscosimetric behaviour and the preferential solvation of syndiotactic, isotactic, and atactic poly(methacrylic acid), [poly(1-carboxy-1-methylethylene)] are studied in water/2-chloroethanol mixtures. The experimental results show that the preferential solvation of the polymer is strongly dependent on its local conformation. In the case of the syndiotactic sample, a close correlation has been established between the compact structure ↔ coil conformational transition and the variation of the preferential and absolute solvation of the polymer by 2-chloroethanol, asserting the importance of hydrophobic interactions in the stabilization of the compact structure. Experimental data concerning the isotactic sample suggest the existence of an “inverse compact structure” in 2-chloroethanol-rich mixtures.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 161
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 497-506 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Circular dichroic studies were made on the conformational change of poly(L-lysine) (PLL) by complex formation with sulfonated polystyrenes (PSS) as functions of pH, temperature and polymer compositions in comparison with the complexes of PLL with sulfated poly(vinyl alcohol) (PVS). The coil-to-helix transition of PLL by complex formation at neutral and acidic pHs, which took place in the PLL/PVS (with high degrees of sulfation) complexes, was prevented in the PLL/PSS complexes due to the less chain flexibility of PSS than PVS. Above pH 11, the α-helix of PLL was partially broken into random coil by complex formation with PSS. The drastic decrease in the solution viscosity by the complex formation revealed a large contraction of PSS chain and subsequently a large strain of the α-helical PLL chain so as to give the breakdown of the α-helix. This is denoted a strain-induced conformational change of PLL. It was found that the α-helix of PLL was thermally stabilized by the complex formation with PSS as in the case of PLL/PVS complexes. A β-to-α transition of PLL by the complex formation with PSS was also found, while the β-form was maintained in the PLL/PVS (with high degrees of sulfation) complexes.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 162
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: 4-Vinylphenylboronic esters 1 and 2 of L-1,2-propandiol (3a) resp. D-mannitol (4a) were polymerized under different conditions to macroporous, crosslinked copolymers. Afterwards the alcohols 3a resp. 4a were split off. The alcohols have thus been used to form chiral microcavities within the polymer, of which those prepared from 1 contain 1 and those from 2 contain 3 binding groups —B(OH)2. Binding sites with 2 binding groups have been investigated before. These polymers possessed capacity for the resolution of the racemate of the template used. The kinetics of the mass transfer within polymers with three binding groups per cavity is discussed in more detail. The chromatographic investigation of the binding ability at different pH-values of polymers from 2 for D-mannitol showed even in acidic media a pronounced binding through neutral esters 5, whereas in alcaline media a much stronger binding through basic esters 6 occurred.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 163
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A number of tetra- and pentaalkylpiperidine derivatives of acrylic and methacrylic acid was synthesized, polymerized, and copolymerized with several comonomers as potential UV stabilizers. In addition, by oxidation of some of these polymers and of a copolymer with peroxy compounds, polymers were obtained containing pendant nitroxyl groups. The properties of these polymers with free radical groups are discussed in relation to their spectral data.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 164
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 643-649 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: (S)-Poly(2-aminobutyric acid) (1) [(S)-poly(imino-1-methyl-3-oxotrimethylene)] was transformed into its N-trifluoroacetyl derivative 4. The IR spectra and the circular dichroism of both substances were compared. In addition, (S)-poly[N-(1-phenylethyl)acrylamide] (2) ((S)-poly-[1-(1-phenylethylaminocarbonyl)ethylene]) was trifluoroacetylated leading to polymer 5. 4 was found to react as trifluoroacetylating agent with L-1-phenylethylamine (L-3) twice as fast as it reacts with D-3. Accordingly, the reaction of 4 with D,L-3 leads preferentially to the L-form of N-(1-phenylethyl)trifluoroacetamide with optical yields up to 6%. The reaction of 5 with D,L-3 affords the D-form of N-(1-phenylethyl)trifluorcacetamide with optical yields up to 13%.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 165
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Binary and ternary copolymerizations of the acrylonitrile (A) / styrene (S) / methyl acrylate (M) system were carried out by emulsion polymerization, using sodium lauryl sulfate as emulsifier and potassium persulfate as initiator. Kinetic studies of the reaction mixture by gas chromatography and simulation calculation of the copolymer composition versus conversion show that the classical theory of copolymerization (propagation rate by Markov chain 1st order) can be applied to the emulsion polymerization of this system, even at high conversion level. It was found that, when a conversion limit is obtained, the polymerization can be started again owing to a new addition of the more rapidly consumed monomer (styrene, in this case); it appears that both polymerization process and conversion effect do not involve appreciable variations of the polymer radical reactivity.
    Additional Material: 18 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 166
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 707-713 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The optical activities of poly(l-menthyl vinyl ether) (PMVE), obtained by cationic polymerization were studied. The polymerizations were carried out at various temperatures (-72 to +30°C), with different solvents and catalysts. The optical rotation of PMVE, which was polymerized with BF3O(C2H5)2 in toluene at -72°C, was found to be independent of the initial monomer concentration; but it depends on the activity of the catalyst. The absolute values of optical rotation of PMVE decreased with increasing temperature and dielectric constant of the solvent. The relationship between the optical activities of PMVE and the polymerization conditions is discussed.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 167
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Isotactic poly-(S)-4-methyl-1-hexene (PS4MH), poly-(R,S)-4-methyl-1-hexene (PRS4MH) and poly-4-methyl-1-pentene (P4MP) were fractionated according to stereoregularity and molecular weight. The fractions obtained were characterized and the constants aη and K of the Mark-Houwink equation calculated for thermodynamically good solvents at low temperatures and for theta solvents at high temperatures.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 168
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 799-808 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Initiation of the polymerization of 2-vinylpyridine by organomagnesium compounds in hydrocarbon solvents, was obtained without side reactions on the pyridine rings. The resulting active centres are unsymmetrical. They are stable and stereospecific, leading to living polymers with an isotacticity degree of about 0,9.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 169
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 857-867 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The viscoelastic properties of poly(α,α-diethyl-β-propiolactone) were investigated in the linear range using stress relaxation and dynamic mechanical methods. Using Ferry's reduction method, a horizontal shift factor was determined at each temperature, that satisfactorily agreed with the WLF equation in the transition zone. No vertical shift was required to superimpose different relaxation curves. The apparent activation energy was temperature dependent and passed through a maximum near Tg whose value is (311 ± 2)K. The relaxation spectrum has been calculated according to the first method of approximation of Schwarzl and Staverman. It consists of a high intensity plateau at shorter times, a wedge type portion with a slope of -0,15 and a low intensity plateau at longer times. Dynamical mechanical measurements revealed a β relaxation peak at 333 K and yielded the evidence of a γ peak around 120 K.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 170
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The thermal polymerization of methyl methacrylate is accompanied by the formation of appreciable amounts of an unsaturated dimer (H-1). The behaviour of H-1 during homopolymerization in presence of an initiator at 60, 80 and 100°C and during copolymerization with MMA in presence of an initiator at 60°C are investigated. The rate of (H-1)-homopolymerization is very low. The transfer constant to monomer H-1 is about CH-1 = 3·10-3 at 80°C as received from Pn-determinations. The termination is essentially by disproportionation. The copolymerization parameters as resulting from polymerizations with labeled MMA at 60°C are rMMA = 1,8 and rH-1 = 0,33, respectively.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 171
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 951-956 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A solution cast layer of ethyl cellulose on aluminium substrate shows high charge acceptance on corona charging. Its surface potential decay characteristics are studied at room temperature and at higher temperatures. Addition of a thermosensitive dye in the polymer matrix shows enhanced contrast potential at constant IR exposure. Optimum conditions for suitability of the polymer in electrothermography is determined by studies on different weight proportions of dye. The effect of layer thickness on surface potential characteristics is also investigated.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 172
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 969-977 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The higher homologues for isotactic (it) poly(1-alkylethylene)s (from it-poly(1-dodecylethylene) to it-poly(1-eicosylethylene)) show three polymorphic modifications. The modification of highest order crystallizes in an orthorhombic structure (modification I). This modification is formed during melt crystallization at a cooling rate φ 〈 2,5 K·s-1. The main-chain conformation is a quaternary helix. The side-chains are tilted 130,6° against the axes of the helices and crystallize like orthorhombic polyethylene. The DSC-curves of these homologues in modification I show the endotherm of melting and an endotherm at a temperature, about 25 K to 30 K below the melting temperature. The endotherm at the lower temperature is caused by atactic material in the samples, by only partially ordered crystallites in isotactic material, and by the change of conformation of some CH2-groups of the side-chains near the main chain.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 173
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 979-984 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Poly[thio(thiocarbonyl)oxy-1,4-cyclohexyleneoxy(thiocarbonyl)thiomethylene-1,4-phenylenemethylene] (4) was obtained from 4-bromomethylbenzyl bromide (1), dipotassium 1,4-cyclohexanediolate (2) and carbon disulfide at low temperature by using 1,4,7,10,13,16-hexaoxacyclooctadecane as catalyst. At high temperatures, poly[oxy-1,4- cyclohexyleneoxymethylene-1,4-phenylenemethylene] (8) was obtained from the reaction between 1 and 2, however. Mechanisms are proposed for these reactions.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 174
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The oxidation of guaiacol by the Fe(III)-oaPc/H2O2 system is studied by using a stopped flow spectrophotometer. The maximum rate of oxidation reaction by this system amounts to about 1000 times that in the absence of H2O2. The kinetic investigation indicates that the reaction can be regarded as “an ordered two-substrates reaction” and that the oxidation reaction proceeds according to the peroxidase-like mechanism. The reaction is inhibited by adding cyanide. The structure of oxidation products is also discussed. The catalytic action of Fe(III)-oaPc in the presence of various polyelectrolytes such as poly(vinylamine) is also investigated, varying the pH values, and the environmental effect of the polymers in their catalytic behavior is discussed.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 175
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 1059-1070 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In this paper, the assignment of the 1H and 13C NMR spectra of poly(galacturonic acid)s is proposed; the 4C1 chair conformation of the monomeric unit in poly(galacturonic acid) is confirmed and the composition of the anomeric mixture at the reducing end (α-D)/(β-D) = 35 : 65 mol/mol independent of the degree of polymerization DP (2 ≤ DP ≤ 5) is given. It is demonstrated on oligomers that both 13C and 1H chemical shifts and coupling constants are nearly unaffected by exchanging Na counterions with Ca; the osmotic coefficient of Ca depends on the DP just as predicted by an electrostatic mechanism. The intrinsic viscosity of the polymer increases and the intensity of 13C NMR signals decreases suddenly for 0,3 equivalents Ca2+ per carboxylic site. These results confirm a multichain association followed by a rigid gel formation; the crosslink is proposed to correspond to a cooperative “egg-box” mechanism on chain segments randomly distributed in the gel.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 176
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 1081-1088 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The asymmetric induction radical copolymerization of styrene (St) with maleic anhydride (MAn) was studied in various solvents with different dielectric constants in the presence of lecithin as a chiral surfactant. The observed specific rotation of the resulting alternating copolymer decreased with an increase in the dielectric constant of the solvent used. It was concluded that the asymmetric induction depends mainly upon the incorporation of MAn within the reversed lecithin micelles.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 177
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 1121-1126 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The influence of morphology in a low density, high melt index polyethylene was studied with particular reference to environmental stress cracking (ESC). Test samples of the polyethylene were molded under constant conditions, only the subsequent rate of cooling to room temperature being changed. Several techniques were used to study the resultant polymer including ESC tests, X-ray diffraction, optical microscopy and constant strain rate stress/strain tests. It was found that the faster the polymer was cooled after molding, the smaller was the typical diameter of the spherulites and the greater the resistance to stress cracking. A hypothesis is proposed to explain the differences in terms of the ease with which a crack can propagate, assuming that propagation is easier in amorphous material than within spherulites.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 178
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 1209-1213 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Spectrophotometric studies in the UV region were carried out for a series of chlorine and bromine derivatives of N-ethylcarbazole and poly(N-vinylcarbazole). All the examined polymers, in the whole spectral range, exhibit considerably less absorptivity than their low molecular models, i.e. ethylcarbazoles. Absorption bands of the polymers are shifted, in comparison to the respective absorption bands of halogenethylcarbazoles, towards shorter wavelenghts. Halogen substituents in the carbazole ring reduce the transfer energy π → π*. This bathochromic effect is especially observable for low-energy bands 1La and 1Lb, and it was noticed that the bromine substituent exerts more influence than the chlorine substituent.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 179
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 1251-1287 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Network structures and physical properties of products obtained either by crosslinking polyepoxides with polyphenols, and by dicyanodiamide or by catalytic polymerization are discussed and compared with those obtained by amine or anhydride curing. The highest crosslinking density is achieved by the polymerization of epoxy compounds. In polymerization, the glass transition temperature may rise by more than Δ Tgv = 100 K. Amine and phenol curing result in similarly structured networks with mobile aliphatic segments and comparatively low crosslinking densities. Impact resistance based on dissipation of mechanical energy increases as network density decreases, a maximum being achieved with a medium chain length of 25 - 35 atom intervals between crosslinking points. The mechanical stability of polymers is limited by the cohesive strength KF. This latter corresponds to the maximum shear strength of bonds TKFmax, which was measured within the temperature range of 77 K to 450 K, in accordance with the equation \documentclass{article}\pagestyle{empty}\begin{document}$ {{\rm TKF}_{\max } = {\rm KF} = B - C \cdot T;} \quad {T 〈 T_g } $\end{document} This equation was derived from Eyring's model of viscosity, correlating B and C with activation volume, activation energy, Tg, and strain rate. B equals the cohesive strength at 0 K. It is determined by intermolecular forces but does not depend on the density of crosslinking. An increase of Tg due to crosslinks or bulky segments causes a decrease of C and therefore a reduction of the temperature dependence of KF. Hence, cohesive strength at room temperature is improved.
    Additional Material: 15 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 180
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 1339-1348 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Copolyesters derived from adipic acid, trans-3-hexenedioic acid and 1,16-hexadecanediol were prepared and investigated by means of X-ray diffraction and DSC techniques. From the X-ray results an isomorphous replacement of the saturated and unsaturated diacid units has been suggested. The equilibrium melting temperature Tm0 and the heat of fusion ΔHf were slightly dependent on the copolyester composition. The crystallization process was analyzed by means of Hoffman's kinetic crystallization theory for a lamellar type crystal growth. The values of the free energy of formation of a nucleus of critical dimensions φ* and the free energy of folding σe were found to decrease regularly with increasing amount of double bonds, varying from 110 to 83 kJ/mol for Δφ* and from 171 to 127 erg/cm2 for σe. This effect has been interpreted on the basis of an increase of chain flexibility owing to the presence of the trans double bonds.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 181
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 1357-1362 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The dependence of the melting temperature on the crystallization temperature for low molecular weight fractions of poly(octamethylene oxide), (poly(oxyoctamethylene)), in the range from Mn = 3400 to Mn = 9 000, is analyzed. It is found that in this molecular weight region, the extrapolated linear relation melting temperature Tm vs. crystallization temperature Tc, for high levels of crystallinity yields an equilibrium temperature, which is in good accord with theoretical expectations; meanwhile the Tm vs. Tc relation for low levels of crystallinity leads to higher equilibrium temperatures. The equilibrium melting temperature corresponds to 356 K for Mn = 9 000 and the enthalpy of fusion was found to be 60,5 cal/g (= 253 J/g).
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 182
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Living oligomers of ethylene obtained by sec-butyllithium complexed with tetramethylethylenediamine (TMEDA) were deactived by oxygen. NMR and mass spectrometry, coupled with gas chromatography of the resulting product allowed us to follow the influence of TMEDA towards functionalization. The two products were characterized. Apparently the ratio [TMEDA]/[sec-BuLi] does not seem to influence the functionalization reaction.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 183
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 1483-1494 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Poly[2-(1-naphthyl)-1,3-dioxan-4,6-diylmethylene] (3), poly[2-(2-naphthyl)-1,3-dioxan-4,6-diylmethylene] (5), 1-naphthalenecarbaldehydetrimethyleneacetal (7) and 2-naphthalenecarbaldehydetrimethyleneacetal (8) were synthesized and characterized by UV- and fluorescencespectroscopy. In addition triplet-triplet absorption maxima and triplet-lifetimes were determined by flash technique. The naphthalene derivates were found to act as donors in the charge-transfer complex formation with such electron acceptors as tetracyanoethylene, 2,5-cyclohexadien-1,4-diylidenedimalonodinitrile and 2,4,5,7-tetranitro-9-fluorenone. The equilibrium constants of the charge-transfer complexes were determined spectrophotometrically by the methods of Benesi-Hildebrand, Benesi-Hildebrand-Scott and Foster-Hammick-Wardley.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 184
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 1513-1524 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Microgels were prepared by crosslinking of poly(vinylalcohol)s with different molecular weights (saponification degree: 88 mole-%) with glutaraldehyde in aqueous solutions. The degree of crosslinking was varied between 0 and 10% (i.e. 10 crosslinks per 100 structural units). Viscosity measurements showed that the viscosity number [η] of the microgels decreases considerably with increasing degree of crosslinking  -  as to be expected with increasing mean density of the random coils: The mean coil volume in aqueous solution shrinks by introducing 10 crosslinks per 100 structural units to 1/10 of the primary volume. A comparison of the logarithmic [η]-M̄-plots of our microgels showed a linear decrease of the exponent a, from a = 0,73 (uncrosslinked) to a = 0,16, with increasing degree of crosslinking. By extrapolation, with a degree of crosslinking of 13% (i.e. 13 cross-links per 100 structural units of polymer chain), it was found that [η] becomes independent of the molecular weight of the primary PVAl-samples.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 185
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: 4-(1,1-Dicyanoethylazo)benzyl methacrylate (3), a new azo-monomer, was copolymerized with styrene, methacrylonitrile, and methyl methacrylate (MMA) giving azo-copolymers. The compositions of the copolymers from 3 and MMA were nearly identical with those of the monomer mixtures. Thus allowing 100% conversion leading to copolymers of almost identical chemical composition. These azo-copolymers were used as initiators for different monomers in either emulsion or solution, resulting in graft-copolymers. The graft-copolymers were characterized by IR and GPC. In one case the raw graft-copolymer was separated into ungrafted backbone-polymer, grafted copolymer, and homopolymer of the component to be grafted.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 186
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 1613-1618 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Effective catalysts for the copolymerization of CO2 with 1,2-epoxypropane were prepared from partially O-methylated or crosslinked poly[1-(4-hydroxyphenyl)ethylene] and Zn(C2H5)2. The highest activity was obtained with catalysts of 30 to 40% methylation or crosslinking. Inactivation of the catalysts during the copolymerization was decreased by crosslinking, increasing the yield of the copolymer. The higher rigidity of the catalyst structure is responsible for its higher activity and stability.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 187
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 1649-1654 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The excluded volume parameter B for poly(N-1,1-dimethyl-3-oxobutylacrylamide) in 2-butanone at 25°C is evaluated either from limiting viscosity numbers or from second virial coefficients as obtained in light scattering measurements, and also through a procedure in which both kinds of experimental data are simultaneously employed. The values so obtained are in reasonable agreement, except for the one evaluated by applying the original Stockmayer-Fixman equation, which is largely underestimated as already found for other polymer-solvent systems.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 188
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The formation constants of electron donor acceptor complexes formed by p-dioxene, α-methylstyrene, phenanthrene, phenyl vinyl ether and styrene as donor molecules and difluoromaleic anhydride as acceptor are much larger compared to those formed by maleic anhydride and the same donor molecules. However, no relation can be established between the numerical value of the formation constant and the tendency of alternating copolymerization induced by radical initiators. Symmetry considerations lead to the conclusion that electron donor acceptor complexes have no significant involvement in this copolymerization. The result of our kinetic investigations in the system phenyl vinyl ether/difluoromaleic anhydride supports the above statement: The formation of the electron donor acceptor complex is not the rate determining step of copolymerization.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 189
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 1747-1755 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The influence of composition on the overall rate of isothermal crystallization of isotactic random propylene/1-butene copolymers is investigated. At a constant crystallization temperature a small fraction of 1-butene co-units inserted along a polypropylene chain causes a drastic reduction in the overall rate of crystallization. Further it is found that for a given rate of crystallization it is possible to crystallize the isotactic polypropylene at lower crystallization temperature by adding along the chain a small amount of 1-butene as comonomer. The equilibrium melting temperature, the surface free energy of folding, the enthalpy and the entropy of fusion decrease with increasing the contents of 1-butene in the copolymer samples.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 190
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The kinetics of the cationic polymerization of trioxane initiated by perchloric acid is analyzed as a simultaneous polymerization and crystallization process. The details of the crystal growth such as nucleation, distribution of crystal sizes, development of growth spirals etc. have been investigated by electron and light microscopic techniques. The mechanism of polymerization can be understood as a catalyzed crystal growth. A well defined population of crystals is formed during a nucleation event at the start of the polymerization. An adsorption equilibrium with regard to the catalyst is then established in the presence of the rather large surface area of the growing polymer crystals. Assuming a Langmuir-type adsorption behaviour, the observed growth features (growth spirals) can be quantitatively interpreted on the basis of the BCF-theory of crystal growth. The current concepts on the molecular mechanism of cationic polymerization of cyclic formals have been modified such as to take into account that each chemical step of the polymerization is a building step of the crystal too.
    Additional Material: 24 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 191
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 1823-1840 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Variously composed copolymers from styrene and 4-vinylpyridine (4-VP) were prepared and their complex formation reactions with benzylbis(dimethylglyoximato)Co(III) [BzCo(III)(DMG)2] and N,N′-ethylenebis(salicylideneiminato)Co(II) (Co(II)salen) were studied kinetically by the stopped-flow rapid scanning spectroscopy. For the complex formation reaction with BzCo(III)(DMG)2, the relationship between the complex formation constant K and the content of 4-pyridylethylene units in the copolymers showed an unusual bell-type curve, and the K values were higher than the K value of complexation with pyridine. From the correlation between K, k (complex formation rate constant), and k′ (complex dissociation rate constant), it resulted that (1) the higher K values of the polymer systems are due to the lower k′ values compared with the pyridine system, and (2) the bell-type change of the K values is also caused by the k′ values. In the case of Co(II)salen-copolymer systems, two species of the complex, i.e., mono- and diaxial coordinated complexes were clearly identified by spectrometric kinetics, whereas the pyridine system gave only a mono-axial coordinated complex. The diaxial coordination seems to lead to a much more favorable structure than the monoaxial one, due to the entropic gain or to the polymer chelate effect.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 192
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 1889-1896 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Hydrolyses of p-nitrophenyl acetate (PNPA) and 3-acetoxy-N,N,N-trimethylanilinium iodide (ANTI) catalyzed by poly[p-vinyl(thiophenol)-co-acrylic acid] (PSH) were studied in the pH range of 8 - 9,5. The reaction of PNPA followed pseudo-first-order kinetics and was found to be catalyzed by the thiophenolate ions on the polymer backbone. In the case of positively charged ANTI, the rate of catalysis showed substrate saturation phenomena and could be described by a Michaelis-Menten kinetics. This indicates that this reaction proceeds via a complex formed by electrostatic interaction between the substrate and the negatively charged polymer catalyst. When ionic strength was increased to 0,12 mol/l the reaction did not further follow the Michaelis-Menten kinetics, suggesting that the complexation constant or the reaction rate of the complex might vary with the amount of the substrate incorporated in the polymer domain. Positively charged N,N,N-trimethylanilinium iodide competively inhibited the PSH-catalyzed hydrolysis of ANTI.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 193
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 1923-1934 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: 1H and 13C NMR investigations were carried out on polystyryl carbanions and model compounds for the active chain end of living polystyrene, changing counter cation (Li, K, and Cs), solvent, and temperature. The structure of the model compounds with K and Cs as counter cation was planar with sp2-hybridized α-carbon, which indicates strongly hindered rotation of the phenyl ring. For the model compound with lithium as counter cation, the phenyl ring rotation was hindered at lower temperatures. The 13C—1H coupling constants of the compound indicated less sp2 character of α-carbon. The differences in the chemical shifts of the two ortho or meta carbons depended on the type of counter cation, suggesting an interaction between counter cation and phenyl ring. Quantum chemical calculations on the structure of the model compounds were carried out and the results were compared with the excess charge distributions calculated from 13C NMR chemical shifts.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 194
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 1987-1998 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Small-angle scattering curves of random coil polymer solutions are calculated from the general scattering theory of solutions by making use of a previous calculation of the Yvon-Born-Green integral equation for the radial distribution function of the solute polymer molecules. The calculated scattering function is a monotonously decreasing function of the scattering angle at low polymer concentration, and it has a minimum and a maximum at high concentration, where the polymer interaction is repulsive. For large scattering angle, the reciprocal values of the scattering function increase almost linearly with sin2(θ/2), where θ is the scattering angle. This calculated result is in qualitative agreement with recent experimental results of X-ray and neutron small-angle scatterings of polymer solutions.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 195
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 2025-2047 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Cross-linked polymers are formed by a new addition polymerization of dimaleinimides with bis(3-aminocrotonic acid)-esters, -amides, or -nitriles. Model reactions show that the derivatives of 3-aminocrotonic acid add to the electrophilic double bond of maleinimide. The resulting succinimid derivatives rearrange thermally to the corresponding pyrrolinones. At higher temperatures, especially in the presence of an excess of maleinimide, a second molecule of maleinimide is added to the pyrrolinone. Some properties of moulded and casted polymers are described.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 196
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: During the reaction of polyamide 6 or polyamide 6,6 with the bifunctional crosslinking agent 1,5-difluoro-2,4-dinitrobenzene in heterogeneous media, 5-fluoro-2,4-dinitrophenylamino groups and 4,6-dinitro-1,3-phenylenediamino groups are formed within the polymer. Owing to their different VIS-spectroscopic behaviour, the concentration of both groups can be determined by means of a bicomponent analysis, \documentclass{article}\pagestyle{empty}\begin{document}$$\begin{array}{*{20}c} {c_1} & {= (15,36 \cdot A_{375} - 6,35 \cdot A_{425}) \cdot 10^{- 5} ({\rm mol} \cdot {\rm dm}^{- 3})} \\ {c_2} & {= (9,48 \cdot A_{425} - 4,78 \cdot A_{375}) \cdot 10^{- 5} ({\rm mol} \cdot {\rm dm}^{- 3})}\\ \end{array}$$\end{document} where c1 and c2 represent the concentration of 5-fluoro-2,4-dinitrophenylamino and 4,6-dinitro-1,3-phenylenediamino groups, respectively, and A375 as well as A425 represent the absorbances at 375 nm and 425 nm, measured in a 1 cm cell (solvent: 2,2,2-trifluoroethanol). N-(5-fluoro-2,4-dinitrophenyl)-ε-aminocaproic acid and N,N'-(4,6-dinitro-1,3-phenylene)-di-ε-aminocaproic acid are used as model compounds in order to calibrate the photometer. It is demonstrated that the degree of crosslinking, determined by means of the bicomponent analysis, is in accordance with the change of molecular weight, determined viscosimetrically.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 197
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 2127-2135 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: 1,2,4,5-Tetracyanobenzene reacts under mild conditions with anionic reagents not to polymer but to low molecular weight, high substituted phthalocyanines: 2,3,9,10,16,17,23,24-octacyanophthalocyanine (3a) and tetrakis(1-imino-3-propoxyisoindolo)porphyrazine (3b). 3a is saponified to the octacarboxyphthalocyanine 3c and converted with hydrazine to tetrakis(1,4-diaminophthalazino)porphyrazine (3d). Low molecular metal chelates are synthesized starting from 3a and 3c. IR- and UV/VIS-spectra are discussed.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 198
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 2175-2181 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The interaction between DNA and dyes such as acridine orange (1), proflavine (2), and 3,8-diamino-5-ethyl-6-phenylphenanthridinium bromide (3) were studied by means of the heat of mixing and UV spectra. From the results obtained, the thermodynamic quantities of DNA-dye complexes were estimated. It is concluded that the intercalation process forms a more stable binding than the stacking process does. Further, in each process, ΔG of DNA-2 and DNA-3 systems is nearly equal to that of the DNA-1 system, but their  -  ΔH and  -  ΔS values are higher than those of the DNA-1 system. The stability of binding in DNA-2 and DNA-3 systems may be governed largely by ΔH, while in the DNA-1 system ΔS may contribute largely to the stability of binding.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 199
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: EDA complex formation between 2,4,7-trinitrofluorenone (TNF) and polyesters bearing pendant 9-carbazolyl groups was studied in ethylene dichloride. The formation constant (K) decreases with increasing length of the main chain repeating units separating pendant donor groups and with decreasing degree of polycondensation. In all cases, the values of K in polymeric systems are larger than those for the monomer model system by factors less than three. Thermodynamic parameters for complex formation were also determined. The general trend of the polymer effect is to increase - ΔH, while the entropy term is not much different from the monomer model system. The origin of polymer effects is interpreted as due not only to neighbouring group effects but also to remote group effects, and simultaneous participation of more than one carbazolyl group in complexing an acceptor molecule is considered. The results are compared with the EDA complex formation by ethylenic polymers and polyurethanes with pendant carbazolyl groups.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 200
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Lithium alkylamide catalyzed addition reaction of N-alkylethylenediamines (1) with styrene was examined. It was found that N-alkyl-N-(2-phenethyl)ethylenediamine (3) was formed selectively in preference to N-alkyl-N′-(2-phenethyl)ethylenediamine (4). The identification of products was carried out by 13C NMR. On the basis of the results obtained, a new type of styrene derivative having a primary amino group (6) was synthesized by lithium alkylamide catalyzed addition reaction of 1 with 1,4-divinylbenzene.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...