放大反应对实验室合成聚苯乙烯-共丙烯酸聚电解质的影响

L. Melo, R. Benavides, G. Martínez, D. Morales-Acosta, L. Da Silva, M. Paula
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引用次数: 0

摘要

磺化苯乙烯-丙烯酸共聚物已被用作燃料电池中可替代的聚电解质膜。在这项工作中,原料共聚物是通过一种经过充分研究的溶液共聚反应方法制备的,但在两种不同容量的反应器条件下:100 mL和3 l。主要思想是扩大共聚物的生产规模,为未来的磺化反应提供足够的材料。反应条件为苯乙烯/丙烯酸的摩尔浓度为94/ 6%,BPO为自由基引发剂的摩尔浓度为0.045%,二乙烯基苯(DVB)为交联剂的摩尔浓度为0.25%,溶剂二乙苯(DEB)与单体的体积比为50/50。温度保持在90°C,系统以200 rpm搅拌2小时,用于两个反应器。GPC法测定共聚物分子量,DSC法测定玻璃化转变(Tg), TGA法测定分解温度(Td)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of the scaling-up the reactions synthesis of the poly(styrene-co-acrylic acid) polyelectrolyte at laboratory level
Sulfonated styrene-acrylic acid copolymers have been used as an alternative polyelectrolyte membrane for applications in fuel cells. In this work, the raw copolymer has been prepared by a well studied solution copolymerization reaction method, but at two different capacity reactor conditions: 100 mL and 3 L. The main idea was to scale up the copolymer production for having enough material for future sulfonation reactions. The reaction conditions consisted of styrene/acrylic acid in a 94/6 % mol, BPO as radical initiator in a 0.045 % mol, divinyl benzene (DVB) as crosslinking agent at 0.25 %mol and the solvent diethyl benzene (DEB) in a 50/50 volume ratio with monomers. Temperature was kept at 90 °C and the system stirred at 200 rpm during 2 hours, for both reactors. Molecular weight of copolymers was obtained by means of GPC, glass transition (Tg) by DSC and decomposition temperature (Td) through TGA analysis.
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