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The Initiating Effect of Vinyl Aromatic and Diene Monomers on the Polymerization of Isobutylene with VCl4

 

作者: L. Toman,   M. Marek,  

 

期刊: Journal of Macromolecular Science: Part A - Chemistry  (Taylor Available online 1981)
卷期: Volume 15, issue 8  

页码: 1533-1543

 

ISSN:0022-233X

 

年代: 1981

 

DOI:10.1080/00222338108056800

 

出版商: Taylor & Francis Group

 

数据来源: Taylor

 

摘要:

The polymerization of isobutylene with VCl4in n-heptane or in the bulk does not proceed in the dark at temperatures lower than -20°C, yet it may be induced by the addition of styrene, α-methylstyrene, p-divinylbenzene, 1,3-butadiene, isoprene, and 2,3-dimethyl-1,3-butadiene. In these cases the polymerizations proceed with variously long induction periods depending on the type of comonomer used. The shortest induction period was observed after the addition of p-divinylbenzene and 2, 3-dimethyl-1, 3-butadiene. In a nonpolar medium the copolymerization of isobutylene with isoprene or butadiene in the dark gives rise to copolymers insoluble in heptane, benzene, and CCl4, while co-polymers formed with the effect of light are soluble. Unlike polymerizations carried out in a nonpolar solution, the polymerization of isobutylene with VCl4in methyl chloride proceeds spontaneously in the absence of protonic coinitiators. Also, soluble copolymers of isobutylene with isoprene or butadiene arise in the copolymerization in methylchloride solution irrespective of the procedure used when the copolymerization is carried out (in the dark or with the effect of light). Polymerizations and copolymerizations carried out both in nonpolar and in polar solutions are inhibited by the presence of oxygen.

 

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