玻璃化转变
缩水甘油醚
双酚
双酚A
聚合物
环氧树脂
高分子化学
材料科学
乙醚
聚合
极限抗拉强度
软化点
化学工程
有机化学
复合材料
化学
工程类
作者
H. Craig Silvis,Jerry E. White,Steven P. Crain
标识
DOI:10.1002/app.1992.070441008
摘要
Abstract A series of novel poly(hydroxy ethers) have been prepared via polymerization of the diglycidyl ethers of bisphenol‐A ( 4 ), 4,4 ′‐tribromotetramethylbiphenol ( 6a ), and 4,4 ′‐tetrabromotetramethylbiphenol ( 6b ) with a variety of rigid diols in an effort to systematically modify structural features of the phenoxy repeat unit in order to control the torsional mobility of polymer backbones and produce materials with softening temperatures higher than are typical for the class. The resulting poly(hydroxy ethers) displyed glass transition temperatures ranging from 109 to 242°C. There of the polymers were characterized with respect to tensile and impact properties and were compared to the polymer sythesized from bisphenol‐A ( 1 ) and bisphenol‐A diglycidyl ether ( 4 ).
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