SELF-CATALYZED CARBON-DIOXIDE INCORPORATION SYSTEM - THE REACTION OF COPOLYMERS BEARING AN EPOXIDE AND A QUATERNARY AMMONIUM GROUP WITH CARBON-DIOXIDE

被引:19
|
作者
KIHARA, N [1 ]
ENDO, T [1 ]
机构
[1] TOKYO INST TECHNOL,RESOURCES UTILIZAT RES LAB,MIDORI KU,YOKOHAMA,KANAGAWA 227,JAPAN
关键词
D O I
10.1021/ma00100a002
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Copolymers of glycidyl methacrylate (GMA) and N-benzyl-N-[2-(methacryloyloxy)ethyl]-N,N-dimethylammonium bromide (1b) were synthesized by radical copolymerization in acetonitrile using AIBN as an initiator to obtain copolymer-6 (GMA:1b=94:6) and copolymer-10 (GMA:1b=90:10), respectively. When copolymer-6 was reacted with carbon dioxide at 100 degrees C in NMP for 24 h, 86% of the epoxide group was converted to the five-membered cyclic carbonate moiety by self-catalyzation, When the powder of copolymer-6 was exposed to carbon dioxide under an atmospheric pressure at 140 degrees C for 500 min, incorporation of carbon dioxide into copolymer-6 was attained up to 76%. Similarly, incorporation of carbon dioxide into copolymer-10 at 130 degrees C for 500 min in the solid state was attained up to 75%. A cross-linked copolymer, copolymer-5C, was synthesized by radical copolymerization of GMA, 1b, and divinylbenzene (93:5:2) and exposed to carbon dioxide to attain 61% of incorporation at 140 degrees C for 500 min.
引用
收藏
页码:6239 / 6244
页数:6
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