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Non-Isothermal Crystallization Kinetics of Poly(ethylene terephalate) /BaSO4 Composites

机译:聚(乙二醇酯)/ BasO4复合材料的非等温结晶动力学

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Three kinds of poly (ethylene terephthalate) (PET)/BaSO4 composites were prepared by melt blending of PET and different surface characteristic BaSO4 of unmodified, organically modified with silane coupling agent, and inorganically coated with SiO2/Al2O3 compound. The crystallization behaviour of the composites and pure PET were studied using differential scanning calorimetry (DSC). The cooling scanning curves showed that the crystallization peak became narrow and melting crystallization temperature (Tmc) shifted largely to high temperature region after the addition of BaSO4. However, the melting temperatures(Tm) of pure PET and PET/BaSO4 composites were not obviously changed, which indicated from the second heating scanning curves. In this research, the Jeziorny method was also employed to describe the non-isothermal crystallization kinetics of pure PET and the PET/BaSO4 composites. The value of Zc increased largely and the half-time of crystallization obviously shortened for the PET/BaSO4 composites. All these results indicated that crystallization ability of PET/BaSO4 composites was remarkably improved in comparison with the pure PET and BaSO4 was a better nucleation agent,especially the inorganically modified one.
机译:通过用硅烷偶联剂的未改性,有机改性的PET和不同表面特征BasO4的熔融混合制备三种聚(对苯二甲酸乙二醇酯)(PET)/ BasO4复合材料制备,并用硅烷偶联剂进行有机改性,并有机涂覆有SiO 2 / Al 2 O 3化合物。使用差示扫描量热法(DSC)研究了复合材料和纯PET的结晶行为。冷却扫描曲线表明,在添加BasO4之后,结晶峰变窄和熔化结晶温度(TMC)在很大程度上在高温区域上移动。然而,纯PET和PET / BasO4复合材料的熔化温度(TM)未明显改变,从第二加热扫描曲线表示。在该研究中,还用于描述纯PET和PET / Baso4复合材料的非等温结晶动力学的非等温结晶动力学。 ZC的值大大增加,并且对于PET / Baso4复合材料明显缩短了半结晶。所有这些结果表明,与纯PET和BasO4相比,PET / BasO4复合材料的结晶能力显着改善,纯PET 4是一种更好的成核剂,尤其是无机改性的药剂。

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