首页 | 本学科首页   官方微博 | 高级检索  
     

TMI和苯乙烯溶液共聚合的竞聚率
引用本文:袁来深,张才亮,顾雪萍,冯连芳.TMI和苯乙烯溶液共聚合的竞聚率[J].浙江大学学报(自然科学版 ),2011,45(10):1862-1867.
作者姓名:袁来深  张才亮  顾雪萍  冯连芳
作者单位:浙江大学 化学工程与生物工程学系 化学工程联合国家重点实验室,浙江 杭州310027
基金项目:化学工程联合国家重点实验室资助项目(SKL-ChE-08D03);浙江省自然科学基金资助项目(Y4090319).
摘    要:以甲苯为溶剂和偶氮二异丁腈(AIBN)为引发剂,研究3 异丙烯基-α,α′-二甲基苄基-异氰酸酯(TMI)和苯乙烯(St)溶液共聚合的竞聚率和共聚产物(PS-co-TMI)的相对分子质量及分子质量分布.通过对共聚物产物的傅里叶红外(FTIR)分析,证实了在低转化率(<6%)下成功合成了PS-co-TMI.引入带荧光性官能团的9 (甲氨基-甲基)蒽(MAMA),通过紫外(UV)确定PS-co-TMI的组成;采用Kelen-Tudos正序和逆序法、YBR法和多元线性回归最小二乘法确定TMI(1)和St(2)的竞聚率为:r1=0.27、r2=0.91.凝胶滲透色谱(GPC)分析表明:TMI与St单体的加料量比增加,PS-co-TMI的相对分子质量和分子质量分布均减小.


Monomer reactivity ratios of TMI and styrene solution copolymerization
YUAN Lai-shen,ZHANG Cai-liang,GU Xue-ping,FENG Lian-fang.Monomer reactivity ratios of TMI and styrene solution copolymerization[J].Journal of Zhejiang University(Engineering Science),2011,45(10):1862-1867.
Authors:YUAN Lai-shen  ZHANG Cai-liang  GU Xue-ping  FENG Lian-fang
Abstract:In the presence of toluene as solvent and azobisisobutyronitrile (AIBN) as initiator, the monomer reactivity ratios of 3-isopropenyl-α,α′-dimethylbenzyl isocyanate (TMI) and styrene (St), and molecular weight and molecular weight distribution of as synthesized copolymer (PS-co-TMI) were analyzed. Fourier infrared (FTIR) analysis of as-synthesized copolymer showed that PS-co-TMI was successfully synthesized under the overall conversions less than 6%. The copolymer composition of PS-co-TMI was determined by ultraviolet (UV) measurement with introducing 9-(methylaminomethyl) anthracene (MAMA) bearing fluorescence groups into PS-co-TMI. Using the methods of positive Kelen-Tudos, reversed Kelen Tudos, YBR and multiple linear regression least square, the reactivity ratios of TMI(1) and St(2) were obtained as r1=0.27, r2=0.91. Gel permeation chromatography (GPC) analysis showed that the molecular weight and molecular weight distribution of PS-co-TMI decreased with the increase of TMI/St feeding ratio.
Keywords:
点击此处可从《浙江大学学报(自然科学版 )》浏览原始摘要信息
点击此处可从《浙江大学学报(自然科学版 )》下载全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号