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  • Polymer and Materials Science  (2)
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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 8 (1964), S. 1709-1717 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: In an effort to develop new techniques for studying the effects of irradiation on high polymers, the influence of molecular weight distribution has been investigated. From general mathematical expressions obtained by Saito, equations have been developed to be used for polymers of Schulz-Zimm distributions, and their mixtures. According to the computations, it should be possible to distinguish between crosslinking and endlinking as alternative mechanisms of network formation, by comparing gelling doses for samples of different initial distributions. From gelling dose determinations for polystyrene samples of different polydispersities, it was confirmed that network formation in irradiated polystyrene takes place through crosslinking, in agreement with mechanisms suggested by several authors. It is believed that the simple technique described should be useful for studying radiation processes in polymers that form networks, especially since the method is insensitive to the extent of degradation.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Measurement of butadiene absorption at constant volume, and of polymer formation, indicated that the rate of polymerization was first order in monomer concentration, up to 1.5 mole/l., and also in initial total catalyst concentration, for given molar ratio of alkyl to titanium ester. The overall activation energy was 11.5 kcal./mole. A fast initiation, accompanied by the evolution of ethylene or a mixture of ethane and ethylene, a relatively slow propagation, and chain transfer to monomer, appeared to be the main steps of the reaction. Termination was essentially absent. Insoluble, gellike material was formed roughly at 20% conversion and was attributed to a random crosslinking, involveing very few crosslinks per molecule, or possibly trifunctional branching. The molecular weight distribution was very narrow. A polymer of over 80% in 1,2 units, having a predominantly syndiotactic structure and about 10% crystallinity, was obtained. In the absence of monomer, the catalyst components reacted rapidly to form complexes, accompanied by strong ethane evolution. A complex series of reactions leading to the possible formation of more than one active species was indicated. The active catalyst suffered bimolecular decomposition on prolonged standing. For optimal molar ratio of alkyl to ester of 5/1, the concentration of active species was estimated as having an upper limit of 4.8 × 10-6 mole/l.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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