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首页> 外文期刊>Biomacromolecules >Readily Controllable Step-Growth Polymerization Method for Poly(lactic acid) Copolymers Having a High Glass Transition Temperature
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Readily Controllable Step-Growth Polymerization Method for Poly(lactic acid) Copolymers Having a High Glass Transition Temperature

机译:玻璃化转变温度高的聚乳酸共聚物的易于控制的逐步增长聚合方法

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摘要

Poly(lactic acid) (PLA) copolymers having a significantly higher glass transition temperature (T_g) than that of high molar mass PLA homopolymers (typically 60 ± 5 °C) were prepared. Lactic acid was copolymerized with 1,4:3,6-dianhydro-D-glucitol (isosorbide, ISB) and succinic acid (SA-2), 1,2,3,4-butanetetracarboxylic acid (BTCA-4) or 1,2,3,4,5,6-cyclohexanehexacarboxylic acid (HCA-6). The highest T_gs obtained for the copolymers containing BTCA-4 and HCA-6 were 80 and 86 °C, respectively. The polymers were prepared by step-growth polymerization in the melt phase, which is an easily operable and simple PLA production method in comparison to the ring-opening polymerization (ROP) route. It was shown that the T_g and the cross-linking induced by the polyfunctional carboxylic acid comonomers could be readily controlled by choosing a suitable polymerization time and temperature. Similar improvement in the T_g as achieved for the copolymers of BTCA-4 and HCA-6 was not observed for linear copolymers containing ISB and SA-2.
机译:制备了具有比高摩尔质量的PLA均聚物(通常为60±5°C)更高的玻璃化转变温度(T_g)的聚(乳酸)(PLA)共聚物。乳酸与1,4:3,6-二脱水-D-葡萄糖醇(异山梨醇,ISB)和琥珀酸(SA-2),1,2,3,4-丁烷四羧酸(BTCA-4)或1, 2,3,4,5,6-环己烷六甲酸(HCA-6)。对于含有BTCA-4和HCA-6的共聚物获得的最高T_gs分别为80和86℃。通过在熔体中逐步生长聚合制备聚合物,与开环聚合(ROP)路线相比,这是一种易于操作且简单的PLA生产方法。结果表明,通过选择合适的聚合时间和温度,可以容易地控制由多官能羧酸共聚单体引起的T_g和交联。对于含有ISB和SA-2的线性共聚物,未观察到与BTCA-4和HCA-6的共聚物所实现的T_g类似的改善。

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