Cationic polymerization of 1,3-pentadiene coinitiated by zinc halides

被引:18
|
作者
Rozentsvet, Victor A. [1 ]
Kozlov, Valery G. [1 ]
Korovina, Nelly A. [1 ]
Ivanova, Valentina P. [2 ]
Kostjuk, Sergei V. [3 ]
机构
[1] Russian Acad Sci, Inst Ecol Volga River Basin, Tolyatti 445003, Russia
[2] SV Lebedev Synthet Rubber Res Inst, St Petersburg 198035, Russia
[3] Belarusian State Univ, Res Inst Phys Chem Problems, Minsk 220030, BELARUS
来源
JOURNAL OF APPLIED POLYMER SCIENCE | 2013年 / 128卷 / 03期
关键词
addition polymerization; catalysts; crosslinking; kinetics; rubber; ALUMINUM TRICHLORIDE; DIENES; PIPERYLENE; CATALYSTS; CHLORIDE; STYRENE;
D O I
10.1002/app.38336
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Technology of industrial production of liquid rubber under trademark SKOP is based on the cationic polymerization of 1,3-penadiene (piperylene) in the presence of TiCl4 or AlCl3-based catalytic systems. The disadvantage of these catalytic systems is the high probability of formation of branched and insoluble fractions due to the chain transfer to polymer. This deteriorates the useful qualities of SKOP. Here we propose the new initiating systems for the cationic polymerization of 1,3-pentadiene based on the homogeneous (dissolved in a minimal amount of diethyl ether) zinc halides (ZnCl2 and ZnBr2) as coinitiators and hydrochloric acid, tert-butyl chloride or trichloroacetic acid as initiators. These initiating systems allow to synthesize fully soluble low molecular weight (Mn = 10003000 gmol1) poly(1,3-pentadiene)s with relatively narrow molecular weight distribution (Mw/Mn < 2.0), which do not contain any high molecular weight and insoluble fractions in the whole range of monomer conversion. The polymers synthesized in the presence of zinc halides possess the same microstructure that those prepared with TiCl4 as coinitiator. (c) 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013
引用
收藏
页码:1771 / 1778
页数:8
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