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Thermal stability of nucleation effect of different beta-nucleating agents in isotactic polypropylene

机译:不同β成核剂在同立性聚丙烯中不同β成核试剂的核心稳定性

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摘要

The thermal stability of nucleation effect of three highly effective beta-nucleating agents, namely an aryl diamide-based nucleating agent (TMB-5), a rare earth complex (WBG-II), and calcium pimelate (Ca-Pi) in isotactic polypropylene (iPP) was investigated by DSC multi-scanning cycles. All three nucleating agents induced iPP to form high contents of beta-crystals. After several thermal cycles, the relative content of beta-phase crystals (K (DSC)) in the nucleated iPP was decreased and the crystallization peak temperature () was also decreased. The K (DSC) and of iPP nucleated with TMB-5, WBG-II, and Ca-Pi were decreased by 0.0477, 0.1257, 0.0603, and 0.97, 2.71, 1.18 A degrees C, respectively. It indicated that the nucleation effect became worse. The nucleation effect of TMB-5 decreased less while that of WBG-II and Ca-Pi was significantly reduced. Thus, the orders of thermal stability for nucleation effect of these three nucleating agents were TMB-5 Ca-Pi WBG-II.
机译:三种高效β-成核试剂的成核效应的热稳定性,即芳基酰胺基成核剂(TMB-5),全同立构聚丙烯的稀土化合物(WBG-II)和钙PIMELATE(CA-PI) (IPP)被DSC多扫描周期调查。 所有三种成核剂诱导IPP形成高含量的β晶体。 在几次热循环之后,核解IPP中β相晶体(K(DSC))的相对含量降低,结晶峰值温度()也降低。 用TMB-5,WBG-II和CA-PI核解的K(DSC)和IPP的IPP分别降低0.0477,0.1257,0.0603和0.97,2.71,118℃。 它表明成核效果变得更糟。 TMB-5的成核效果降低,而WBG-II和CA-PI的效果显着降低。 因此,对于这三种成核剂的成核效应的热稳定性的序列是TMB-5> ca-pi& WBG-II。

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