Non-isothermal crystallization kinetics of montmorillonite filled β-isotactic polypropylene nanocomposites

被引:17
|
作者
Dai, Xin [1 ]
Zhang, Zishou [1 ]
Chen, Chunyan [1 ]
Li, Mei [1 ]
Tan, Yunhong [1 ]
Mai, Kancheng [1 ]
机构
[1] Sun Yat Sen Univ, Guangdong Prov Key Lab High Performance Polymer B, Key Lab Polymer Composites & Funct Mat, Minist Educ,Mat Sci Inst,Sch Chem & Chem Engn, Guangzhou 510275, Guangdong, Peoples R China
关键词
Polypropylene; Montmorillonite; beta-Nucleation; Non-isothermal crystallization kinetics; GLASS-FORMING MELTS; POLYMER NANOCOMPOSITES; CATALYZED NUCLEATION; PHASE-CHANGE; BEHAVIOR; FRACTURE;
D O I
10.1007/s10973-015-4635-8
中图分类号
O414.1 [热力学];
学科分类号
摘要
Montmorillonite filled isotactic polypropylene nanocomposites (iPP/MMT) generally form alpha-modification due to the heterogeneous alpha-nucleation of MMT for iPP crystallization. To obtain MMT filled beta-iPP nanocomposites, MMT with beta-nucleating surface (beta-MMT) was prepared by supporting calcium pimelate (CaPA) as beta-nucleator on the surface of MMT particles. The crystallization behavior, melting characteristics, and non-isothermal crystallization kinetics and crystallization activation energies of MMT and beta-MMT filled iPP nanocomposites were studied by differential scanning calorimetry. It is found that the crystallization peak temperatures of beta-MMT filled iPP nanocomposites were higher than those of beta-iPP and MMT filled iPP nanocomposites, which indicated that the heterogeneous nucleation of beta-MMT is stronger than that of MMT. Jeziorny and Mo methods were applicable to study the non-isothermal crystallization kinetics of iPP and its nanocomposites. Addition of CaPA, MMT and beta-MMT can increase the crystallization rate. The crystallization activation energies were calculated by Friedman methods, and nucleating activities were calculated by Dobreva methods. It is indicated that beta-nucleation decreased the crystallization activation energy of iPP, and the nucleating activity of beta-MMT is higher than that of CaPA and MMT.
引用
收藏
页码:829 / 838
页数:10
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