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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 16 (1978), S. 3025-3030 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 673-681 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The rate of n-butyl vinyl ether polymerization by chromyl chloride is first order in [catalyst] and second order in [monomer]. Added H2O (after a certain concentration) and HCl increase the rate, thiophene retards the rate, while pyridine inhibits the rate. DP is independent of [chromyl chloride] and increases with increasing [monomer] up to 1M, thereafter becoming independent of it. Both rate and DP increase over the range 10-32°C and decrease at higher temperatures.
    Additional Material: 4 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 1155-1166 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of polyesters containing conjugated diacetylenic groups in the polymer backbone were synthesized by interfacial condensation of 3,5-hexadiyne-1,6-diol and diacid chlorides of succinic, glutaric, adipic, azealic, sebacic, terephthalic, and isophthalic acids. The polyesters were characterized by their infrared and ultraviolet absorption spectra, elemental analysis, and viscosity measurements. Powder x-ray patterns indicated high degress of crystallinity. The polyesters were found to be highly photoreactive. The relative photoreactivities of the polyester films were determined by the adhesion method. Only small differences in the reactivity have been observed despite structural changes in the R group in the polymer backbone. Differential thermal analysis behavior of all polymers in the temperature range ambient to 300°C and isothermal behavior of HGI at two different temperatures have been studied.
    Additional Material: 7 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 2017-2026 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A low temperature solution condensation method with pyridine as acceptor-catalytic reagent was applied to the synthesis of polyarylates from carbazole and bisphenol A/phenolphthalein. The polyarylates were classified with respect to their structure, thermal stability, and dielectric behavior.
    Additional Material: 4 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 3081-3092 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In the presence of ZnEt2 the CoCl2-quinoline complex polymerizes NVC with a rate increasing with ZnEt2 and CoCl2-Q concentrations up to a certain concentration of ZnEt2 or CoCl2-Q, thereafter becoming independent of either. At a fixed concentration of ZnEt2 and CoCl2-Q the rate is second order with respect to NVC. The poly(NVC) obtained is freely soluble in benzene but leaves some insoluble fraction in methyl ethyl ketone, which has been characterized by 13C-NMR to be a stereoblock polymer. X-ray diffraction, IR, and thermal characteristics of the polymer have also been reported. [η] is virtually independent of monomer, in the concentration range 0.1-0.25 mol/L ZnEt2 and CoCl2-Q concentrations. Oxygen as an additive inhibits the polymerization. A cationic coordination mechanism has been proposed and appropriate rate and degree of polymerization equations have been suggested.
    Additional Material: 5 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 21 (1983), S. 1861-1866 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 23 (1985), S. 2567-2578 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The polymerization of N-vinylcarbazole has been carried out at 60°C under nitrogen with different grades of carbon black, N220, N110, N330, and N660 as heterogeneous catalysts. The order of efficiency of the catalysts in regard to the polymerization is: N220 〉 N110 〉 N660 〉 N330. Effect of solvent polarity on the polymerization has been studied with acetonitrile, 1,2-dichloroethane, and toluene-nitrobenzene mixtures. Nitrobenzene, with highest polarity, affords the highest rate, which decreases with decreasing nitrobenzene percentage in the solvent mixture. These features suggest the polymerization to be cationic in nature. The relative viscosities of the polymers are low, but tend to increase only slightly with increasing nitrobenzene content. The rate of polymerization can be expressed by the relation \documentclass{article}\pagestyle{empty}\begin{document}$$ - \frac{{{\rm d}\left[ {\rm M} \right]}}{{{\rm dt}}} = k_1 [{\rm M}]{\rm [Carbon Black]} $$\end{document} A suitable kinetic model has been presented in conformity with the experimental findings.
    Additional Material: 3 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 23 (1985), S. 2631-2646 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Kinetics of polymerization of N-vinylcarbazole over Co(II)-13X molecular sieves in toluene have been studied. The rate of polymerization (Rp) has been found to be second order with respect to percent exchange level of Co(II) and also to the NVC concentration at all the reaction temperatures of 40, 50 and 60°C. The rate increases with decreasing pH of the original exchanging salt solution up to a pH of about 3.5, beyond which it falls. The overall activation energy of polymerization has been found to decrease with increase in monomer concentration, exchange level of Co(II), and the hydrogen ion concentration of the original exchange solution. Average degree of polymerization also follows a similar trend. A mechanism of polymerization involving simultaneous propagation on both metal ion Co(II) and proton on a zeolite surface has been suggested. The two propagation routes are characterized by an average activation energy of 10.36 kcal/mol and 5.40 kcal/mol on the metal ion and proton centers, respectively.
    Additional Material: 8 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 7-25 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The polymerization of N-vinylcarbazole (NVC) initiated by AsCl3 in benzene and nitrobenzene solvents was studied at 33°C. Rp is proportional to the first power of the initiator concentration. Rp varies in a first-order manner with NVC concentration up to a certain optimum concentration of the latter, after which it falls and ultimately levels off. The rate and the molecular weight are depressed by the addition of various amines, preformed poly-NVC, and water. HCl does not have any cocatalytic effect on the system. Rate and the molecular weight are increased in nitrobenzene. The degree of polymerization stays independent of the initiator and NVC concentration and also of increasing conversion. These results suggest a conventional cationic mechanism, and overrule the possibility of a cation radical initiation. A suitable kinetic scheme has been proposed in conformity with the findings.
    Additional Material: 11 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 12 (1974), S. 1337-1343 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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