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E 51环氧树脂固化反应中动力学转变
引用本文:吴唯,刘明昌,陈玉,浦伟光,吴祥.E 51环氧树脂固化反应中动力学转变[J].复合材料学报,2011,28(4):1-6.
作者姓名:吴唯  刘明昌  陈玉  浦伟光  吴祥
作者单位:华东理工大学 材料科学与工程学院, 上海 200237
摘    要:采用等温DSC法研究了E-51环氧树脂与4, 4’-二氨基二苯基砜(DDS)体系的固化反应过程, 并与已有固化模型拟合得到了170、180、190、200 ℃下的等温固化反应动力学的参数, 根据决定系数R2确定了适合的固化模型。研究表明: 当固化度小于40%时属于Kamal自催化模型; 当固化度大于40%时属于n级固化模型, 即固化反应由Kamal自催化反应向n级反应转变。 

关 键 词:E-51环氧树脂    等温DSC    固化动力学    n级模型    Kamal模型
收稿时间:2010-08-19

Shifting of the curing kinetics of E-51 epoxy resin
WU Wei,LIU Mingchang,CHEN Yu,PU Weiguang,WU Xiang.Shifting of the curing kinetics of E-51 epoxy resin[J].Acta Materiae Compositae Sinica,2011,28(4):1-6.
Authors:WU Wei  LIU Mingchang  CHEN Yu  PU Weiguang  WU Xiang
Affiliation:School of Materials Science and Engineering, East China University of Science &|Technology, Shanghai 200237, China
Abstract:The cure reaction kinetics of E-51 epoxy resin and 4,4’-diaminodiphenylsulfone(DDS) system was investigated by the isothermal DSC method, and isothermal curing kinetics parameters at 170, 180, 190, 200 ℃ were obtained through fitting between the experimental data and the curing model. According to the values of coefficient of determination (R2) of the fitted data, a suitable curing reaction kinetic model was determined. The reaction process shows to be dominated by different mechanism at different stages of the E-51/DDS system curing process, when the cure degree is less than 40%, the curing system is Kamal autocatalytic reaction model; when the cure degree is more than 40%, the curing system is nth order reation model, with an initial autocatalytic reaction shifting into an nth order reaction as the reaction proceeding. 
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