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作 者:崔东霞[1,2]
机构地区:[1]山西省交通科学研究院,山西太原030006 [2]黄土地区公路建设与养护技术交通行业重点实验室,山西太原030006
出 处:《粘接》2015年第5期61-64,68,共5页Adhesion
基 金:山西省交通厅科研计划项目(编号:2014-1-7)
摘 要:采用非等温DSC法对环氧树脂E-51/低温固化剂J005H-2/稀释剂692体系的固化反应动力学进行了研究。应用kissinger法和Flynn-Wall-Ozawa法计算得到了692不同掺量的E-51/J005H-2体系的固化反应动力学参数,并求得固化反应速率方程。结果表明,上述2种方法计算出的动力学参数相近,并验证了该体系符合n级反应模型原理。稀释剂的掺入以及掺量对整个体系的表观活化能有影响,稀释剂掺量为10%时,其活化能达到最低。低温固化剂体系的活化能与固化特征温度(初始、峰顶、完成)均低于常温固化剂体系,尤其是初始开始温度。The curing kinetics of epoxy resin E-51/low-temperature curing agent J005H-2/diluent 692 system was studied by non-isothermal different scanning calorimetry (DSC) .The curing kinetic parameters of the systems with different diluent 692 amount were calculated by Kissinger method and Flynn-Wall-Ozawa method. The curing reaction rate equations of above-mentioned systems were also obtained. The results showed that the kinetic parameters calculated by both the methods were similar, The curing reaction was consistent with the principle of n-th order reaction model. The usage and content of diluent692 had an impact on the activation energy. When the content is 10%, the activation energy touched the bottom .The characteristic temperatures (initial, peak, final) were all lower than those of normal temperature curing agent system, particularly the initial temperature.
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