首页> 外文期刊>Polymer: The International Journal for the Science and Technology of Polymers >Control of the confined and unconfined crystallization in glassy-crystalline poly(vinylcyclohexane)-b-poly(ethylene)-b-poly-(vinylcyclohexane) triblock copolymer in solution
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Control of the confined and unconfined crystallization in glassy-crystalline poly(vinylcyclohexane)-b-poly(ethylene)-b-poly-(vinylcyclohexane) triblock copolymer in solution

机译:控制溶液中玻璃状聚(乙烯基环己烷)-b-聚(乙烯)-b-聚(乙烯基环己烷)三嵌段共聚物的受限和无限制结晶

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摘要

The influence of the solvent evaporation rate on the crystallization of the poly(vinylcyclohexane)-b-poly(ethylene)-b-poly(vinylcyclohexane) (PVCH-PE-PVCH) triblock copolymer with the high T_g of PVCH segment in chloroform was investigated.The competition between the crystallization of PE block and the vitrification of PVCH in the triblock copolymer was controlled through changing the solvent evaporation rate in the solution system at different temperatures (T_e).It was found that the melting temperature (Tm) of PVCH-PE-PVCH samples increased with increasing the T_e when the T_e was lower than the solvent boiling point (bp),depending on the crystalline temperatures.However,when T_e was just a little above the solvent bp,two melting peaks,which corresponding to the fusion of the confined and unconfined crystals,respectively,were observed on the DSC curves of the samples.As T_e increased to be higher temperature,only one lower melting peak,which corresponding to the fusion of the confined crystals,existed for each samples.It was also found that the crystallinity (X_c) of the samples decreased gradually when T_e was lower than the solvent bp,and then decreased suddenly when T_e was just a little above the solvent bp,finally reached a plateau (about 13.5%) at higher T_e.The changes in X_c of the samples depend on the evaporating time in the solution.The results should be related to the competition between the crystallization of PE block in solvent and the vitrification of PVCH block with the solvent evaporation.Furthermore,the competition was controlled through changing the solvent evaporation rate.The confined and unconfined crystallization of the samples could be freely adjusted.
机译:研究了溶剂蒸发速率对在氯仿中具有高T_g T_g的聚(乙烯基环己烷)-b-聚(乙烯)-b-聚(乙烯基环己烷)(PVCH-PE-PVCH)三嵌段共聚物结晶的影响通过改变溶液体系在不同温度(T_e)下的溶剂蒸发速率来控制三嵌段共聚物中PE嵌段的结晶与PVCH的玻璃化之间的竞争,发现PVCH-的熔融温度(Tm)当T_e低于溶剂沸点(bp)时,PE-PVCH样品随T_e的增加而增加,取决于晶体温度。但是,当T_e略高于溶剂bp时,有两个熔融峰,分别对应于在样品的DSC曲线上分别观察到了受限和未受限晶体的熔融。随着T_e升高到较高的温度,只有一个较低的熔融峰,这对应于受限的熔融还发现每个样品都存在d个晶体。还发现,当T_e低于溶剂bp时,样品的结晶度(X_c)逐渐降低,而当T_e稍高于溶剂bp时,样品的结晶度突然降低,最终达到a。在较高的T_e时达到平稳(约13.5%)。样品X_c的变化取决于溶液中的蒸发时间,其结果应与PE嵌段在溶剂中的结晶与PVCH嵌段在玻璃化中的竞争有关。此外,通过改变溶剂的蒸发速率可以控制竞争。可以自由调节样品的受限和无限制结晶。

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