节点文献

DMC催化CO2和环氧丙烷的调节共聚反应及其影响因素

Regulated Copolymerization of Carbon Dioxide and Propylene Oxide with DMC Catalyst and Effects of Reaction Conditions

  • 推荐 CAJ下载
  • PDF下载
  • 不支持迅雷等下载工具,请取消加速工具后下载。

【作者】 周统昌邹志强刘言平罗建新张敏陈立班

【Author】 Tongchang Zhou1,2,Zhiqiang Zou1,2,Yanping Liu1,2,Jianxin Luo1,2,Min Zhang1,Liban Chen1(1.Guangzhou Institute of Chemistry,Chinese Academy of Science,Guangzhou 510650,China;2.Graduate School of the Chinese Academy of Science,Beijing 100039,China)

【机构】 中国科学院广州化学研究所中国科学院研究生院

【摘要】 以聚醚多元醇、二缩三乙二醇或季戊四醇作为分子量调节剂,用Zn-Co双金属氰化物(DMC)高效催化CO2和环氧丙烷(PO)调节共聚合成了数均分子量为3000~8000的多官能度脂肪族聚碳酸酯多元醇,共聚物的分子量基本符合设计要求。几种分子量调节剂均能成功合成两官能度或四官能度的共聚产物,产物中碳酸酯键含量最高可达60%,催化效率最高达663 g/g催化剂,副产物最低可控制到4%。文中还考察了温度、压力、调节剂及催化剂用量对共聚反应的影响,发现60℃的低温更有利于CO2和环氧丙烷的共聚反应,而且要获得碳酸酯键含量较高的产物,需控制调节剂和催化剂的比例。

【Abstract】 A group of multi-functional aliphatic polycarbonate polyols(APC),molecular weight between 3000 and 6000,was synthesized by regulated copolymerization of carbon dioxide and propylene oxide(PO) on double metal cyanide complex(Co-Zn DMC)catalyst with polyether alcohol,pentaerythritol(PER) or triethylene glycol as regulators.The molecular weight of the copolymer complied with the design requirements.All the regulators could successfully produce copolymers with two or four functionality.In the mean time the highest carbonate content of the copolymer is up to 60% and the highest catalystic efficiency could get to 663g of polymer /g of catalyst,with cyclic carbonate is only 4%.In this paper we also examined the effect of the temperature,pressure and the dosage of regulator on reaction.The results reveal that 60 ℃ is in favor of the copolymerization.The regulator and catalyst should be controlled in certain proportion to get high carbonate content.

【关键词】 双金属氰化物催化剂调节共聚CO2环氧丙烷
【Key words】 DMCcopolymerizationcarbon dioxidePO
【基金】 广东省自然科学基金资助项目(9151065004000005);广东省工业攻关项目(2008B010600046)
  • 【文献出处】 高分子材料科学与工程 ,Polymer Materials Science & Engineering , 编辑部邮箱 ,2011年11期
  • 【分类号】TQ316.338
  • 【被引频次】3
  • 【下载频次】275
节点文献中: 

本文链接的文献网络图示:

本文的引文网络