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Synthesis of Polyketone STCO Promoted by Rare Earth Catalyst

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【作者】 郭锦棠郑勇辉王博田晶

【Author】 GUO Jintang ZHENG Yonghui WANG Bo TIAN Jing School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072, China

【机构】 School of Chemical Engineering and Technology Tianjin University Tianjin 300072 ChinaSchool of Chemical Engineering and Technology Tianjin University Tianjin 300072 China

【摘要】 <正>To lower the cost of polyketone synthesis, rare earth coordinate catalyst was introduced to the copoiymerization of carbon monoxide (CO) and styrene (ST) to synthesize aliphatic polyketone STCO. The catalytic system was composed of rare earth neodymium acetate, yttrium acetate, 2,2’-bipyridine, p-toluensulfonic acid, cupric p-toluensulfonate, and 1,4-benzoquinone. The catalyst and the copolymer were characterized by infrared spectrum and X-ray photoelectron spectrosco py respectively. The effects of each component of catalytic system and the kinds of rare earth acetates on catalytic activity of copoiymerization were investigated. The results show that the proposed rare earth has distinct catalytic activity in the copoiymerization of CO and ST and the maximum activity can reach 303.3 gSTCO/(mol·h).

【Abstract】 To lower the cost of polyketone synthesis, rare earth coordinate catalyst was introduced to the copoiymerization of carbon monoxide (CO) and styrene (ST) to synthesize aliphatic polyketone STCO. The catalytic system was composed of rare earth neodymium acetate, yttrium acetate, 2,2’-bipyridine, p-toluensulfonic acid, cupric p-toluensulfonate, and 1,4-benzoquinone. The catalyst and the copolymer were characterized by infrared spectrum and X-ray photoelectron spectrosco py respectively. The effects of each component of catalytic system and the kinds of rare earth acetates on catalytic activity of copoiymerization were investigated. The results show that the proposed rare earth has distinct catalytic activity in the copoiymerization of CO and ST and the maximum activity can reach 303.3 gSTCO/(mol·h).

【基金】 Supported by National Natural Science Foundation of China (No. 20476080).
  • 【文献出处】 Transactions of Tianjin University ,天津大学学报(英文版) , 编辑部邮箱 ,2006年03期
  • 【分类号】O643.36
  • 【下载频次】22
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