logo.gif (2519 bytes)

弹性体
CHINA ELASTOMERICS
2000 Vol.10 No.3 P.8-10

qklogo.gif (1030 bytes)


N-丁基马来酰亚胺/丙烯酸丁酯的共聚研究

谭红艳 刘朋生

  摘要:研究了N-丁基马来酰亚胺与丙烯酸丁酯 的溶液共聚,考察了原料配比、反应温度和 溶剂极性等因素对共聚反应的影响,并用IR、DTA和特性粘数[η]等对共聚产物进行了表 征。
  关键词:N-丁基马来酰亚胺;丙烯酸丁酯;共聚物;溶液共 聚
  中图分类号:O631.5  文献标识码:A  文章编号:1005-3174(2000)03-0008-03

Study on copolymerization of N-Butyl
maleimide and butyl acrylate

TAN Hong-yan,LIU Peng-sheng
(College of Chemistry and Chemical Engineering Xiang Tan U niversity,Xiang tan 410005,China)

ABSTRACT

  In this paper,poly(NBMI-co-BA)was synthesized by solution copolymeriz ation in chloroform.The effect of monomer feed,polymerization temperature and so lvent polarity on polymerization were investigated.In addition,the resulting cop olymers were characterized by IR,DTA and intrinsic viscosity.
  Key words:N-Butyl maleimide;butyl acrylate;solution copol ymerization;copolymers

作者简介:谭红艳(1976—),女,湘潭大学高分子化学和物 理专业硕士,主要从事N-取代马来酰亚胺共聚改性的研究。
谭红艳(湘潭大学化学化工学院,湖南湘潭 410005)
刘朋生(湘潭大学化学化工学院,湖南湘潭 410005)

参考文献:
[1] SHAN Guorong,Kinectic Treatment for Copolymerization of Styre ne or Methyl Methacrylate with N-phenylmaleimide[J].Chinese Journal of Chemical.Engineer Volume 8 Num.12000.(1-5).
[2] Takayuki Otsu.,Reactivity in radical polymerization of N-substituted mal eimides and thermal stability of the resulting polymers[J],Polym.Bulletin.1990 ,23:43-50.
[3] Xu Lin Jiang,Radical Copolymerization Between Methyl Methacrylate and N-c yclohexyl maleimide with Thiol as an Inifer[J].Appl.Polym.Sci.1999,74(6):14 17-1427.
[4] X.Jiang.H.Tai.Kinetics for Copolymerization of MMA with N-cyclohexylmale imide.[J].Appl.Polym.Sci.1999,74(5),1293-1297.
[5] J.LOKAJ.Synthesis and Characterization of Styrene-N-Butyl Maleimide Cop ol ymers Using Iniferters Containing Thiyl End Groups.[J] Appl.Polym.Sci.1998,67 :755-762.
[6] 单国荣.N-取代马来酰亚胺型高分子耐热改性剂的研究进展[J].高分子材料,1 996,(2):36-39.
[7] 赵优良,刘朋生.苯乙烯/N-取代马来酰亚胺共聚合研究[J].弹性体,2000,(1) :10-12.
[8] 赵优良,吴宇雄,刘朋生.N-丁基马来酰亚胺微乳液共聚合研究.I合成与表征[J] .弹性体,1999,9(2):19.
[9] A.L.Schwartz and L.M.Lemer.[J].J.Org.Chem.,1974,39:21.

收稿日期:2000-06-06

请看PDF全文