首页 | 本学科首页   官方微博 | 高级检索  
     

RIM聚氨酯弹性体预聚物的反应动力学研究
引用本文:李再峰,辛浩波,刑政,孙学红,吕锡元,杨光华.RIM聚氨酯弹性体预聚物的反应动力学研究[J].青岛科技大学学报,1998(4).
作者姓名:李再峰  辛浩波  刑政  孙学红  吕锡元  杨光华
作者单位:青岛化工学院,石油大学
基金项目:国家计委“八五”重点科技攻关资助项目
摘    要:在四个不同的温度下研究了四氢呋喃聚醚(PTMG),三羟甲基丙烷混合多元醇和甲苯二异氰酸酯(TDI)的反应。无论是催化的还是非催化的反应,异氰酸根和羟基的反应均遵循二级反应力学,但4-位和2-位异氰酸根具有不同的反应活性。计算了4-位,2-位异氰酸根分别和羟基反应的速度常数k1,k2。活化参数Ea1,Ea2,△≠S1,△≠S2。随着反应体系的温度升高和催化剂m-乙氧基三苯基铋(m-OET-TPB)的加入,k1/k2的比值减小。

关 键 词:反应注射成形  聚氨酯弹性体预聚物  动力学

Reaction Kinetics of RIM Pu Prepolymer
Li Zaifeng Xin Haobo,Xing Zheng,Sun Xuehong lu Xiyuan.Reaction Kinetics of RIM Pu Prepolymer[J].Journal of Qingdao University of Science and Technology:Natutral Science Edition,1998(4).
Authors:Li Zaifeng Xin Haobo  Xing Zheng  Sun Xuehong lu Xiyuan
Abstract:The uncatalyzed and catalyzed bulk polymerizations of polytetrahydrofuran (PTMG) and trimethylolpropane(TMP) with toluene diisocyanate had been studied at four different tempertures. Discontinuity was obtained in the second order plots ofuncatalyzed and catalyzed reaction. The rate constants( k 1,k 2 ) and the activation parameters( Ea 1,Ea 2,Δ ≠S 1,Δ ≠S 2) for the isocyanate groups at the 4 and 2 positions were respectively calculated. The rate constant k 2 increased faster than k 1 and the ratio of k 1/k 2 decreased with added catalyst(m OET tribenzene bismuth) and increased temperture of the reaction system.
Keywords:RIM  polyurethane prepolymer  kinetics  
本文献已被 CNKI 等数据库收录!
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