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Catalytic Chain Transfer Copolymerization of Propylene Oxide and CO2 using Zinc Glutarate Catalyst

机译:谷氨酸锌催化剂催化环氧丙烷与CO2的催化链转移共聚合

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摘要

Oligo and poly(propylene ether carbonate)‐polyols with molecular weights from 0.8 to over 50 kg/mol and with 60–92 mol % carbonate linkages were synthesized by chain transfer copolymerization of carbon dioxide (CO2) and propylene oxide (PO) mediated by zinc glutarate. Online‐monitoring of the polymerization revealed that the CTA controlled copolymerization has an induction time which is resulting from reversible catalyst deactivation by the CTA. Latter is neutralized after the first monomer additions. The outcome of the chain transfer reaction is a function of the carbonate content, i. e. CO2 pressure, most likely on account of differences in mobility (diffusion) of the various polymers. Melt viscosities of poly(ether carbonate)diols with a carbonate content between 60 and 92 mol % are reported as function of the molecular weight, showing that the mobility is higher when the ether content is higher. The procedure of PO/CO2 catalytic chain copolymerization allows tailoring the glass temperature and viscosity.
机译:通过二氧化碳(CO2)和环氧丙烷(PO)的链转移共聚反应,合成了分子量为0.8至50 kg / mol以上且碳酸酯含量为60-92 mol%的低聚和聚(碳酸亚丙酯)多元醇。谷氨酸锌。在线监测聚合反应表明,CTA控制的共聚反应有一个诱导时间,这是由CTA可逆的催化剂失活导致的。加入第一批单体后,中和剂被中和。链转移反应的结果是碳酸盐含量的函数,即。 e。 CO2压力,很可能是由于各种聚合物的迁移率(扩散)不同所致。据报道,碳酸酯含量在60-92 mol%之间的聚(醚碳酸酯)二醇的熔体粘度是分子量的函数,表明当醚含量较高时,迁移率也较高。 PO / CO2催化链共聚的过程可以调整玻璃的温度和粘度。

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