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氯丁胶乳乳液接枝甲基丙烯酸甲酯的反应动力学
引用本文:张凯,黄春保,沈慧芳,陈焕钦.氯丁胶乳乳液接枝甲基丙烯酸甲酯的反应动力学[J].应用化学,2010,27(10):1144-1148.
作者姓名:张凯  黄春保  沈慧芳  陈焕钦
作者单位:(1.湖北黄冈师范学院化学与应用化学学院 黄州 438000;2.华南理工大学化学与化工学院 广州)
基金项目:黄冈师范学院博士基金 
摘    要:采用乳液聚合法将甲基丙烯酸甲酯(MMA)接枝到氯丁胶乳上,红外光谱和核磁共振氢谱证实了接枝产物的生成。 研究了反应温度、乳化剂浓度、引发剂浓度和单体浓度对表观聚合速率的影响。 结果表明,当反应温度为50 ℃,引发剂叔丁基过氧化氢 四乙烯五胺(t-BHP/TEPA)用量为氯丁胶乳干重的0.5%,单体/聚合物质量比m(M)∶m(P)=3∶5,乳化剂十二烷基连苯醚二磺酸钠(DSB)用量为单体总质量1%时,单体转化率和接枝效率分别为99.1%和54.9%。 聚合反应动力学关系式为:Rp=Kc(E)0.15c(I)0.30c(MMA)1.41,式中,K为常数,在40~55 ℃范围内,聚合反应的表观活化能Ea=60.2 kJ/mol。 接枝聚合基本符合自由基反应机理。

关 键 词:氯丁胶乳  乳液接枝聚合  动力学  甲基丙烯酸甲酯  接枝机理  
收稿时间:2009-10-30
修稿时间:2010-02-05

Kinetics of Grafting Polymerization of Chloroprene Latex with Methyl Methacrylate by Emulsion Polymerization
ZHANG Kai,HUANG Chun-Bao,SHEN Hui-Fang,CHEN Huan-Qin.Kinetics of Grafting Polymerization of Chloroprene Latex with Methyl Methacrylate by Emulsion Polymerization[J].Chinese Journal of Applied Chemistry,2010,27(10):1144-1148.
Authors:ZHANG Kai  HUANG Chun-Bao  SHEN Hui-Fang  CHEN Huan-Qin
Institution:(1.School of Chemistry and Applied Chemistry,Huanggang Normal University,Huangzhou 438000; 2.School of Chemistry and Chemical Engineering,South China University of Technology,Guangzhou)
Abstract:Grafting of methyl methacrylate(MMA) onto chloroprene latex was carried out by emulsion polymerization. FTIR and 1H NMR confirmed that the grafted polymer was formed. Effects of the reaction temperature, the emulsifier concentration, the initiator concentration and the monomer concentration on the apparent polymerization rates were investigated. The results showed that the monomer conversion and the grafting efficiency could reach 99.1%, 54.9%, respectively, under the conditions where the reaction temperature was 50 ℃, the dosage of initiator tert-butyl hydroperoxide/tetraethylenepentamine(t-BHP/TEPA) was 0.5%(based on the mass of dry chlorene rubber latex(CRL)), mass ratio of monomer to polymer was 3∶5, and the amount of emulsifier sodium dodecylbenzenesulfonate(DSB) was 1%(based on the mass of monomer). The kinetics equation Rp=Kc(E)0.15c(I)0.30c(MMA)1.41, where K is a constant, was obtained. The overall activation energy for the polymerization process was 60.2 kJ/mol within 40~55 ℃. The graft-copolymerization reaction follows the free radical mechanism generally.
Keywords:chloroprene latex  emulsion graft polymerization  kinetics  methyl methacrylate  grafting mechanism
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