Nonisothermal Crystallization Kinetics and Microhardness of PP/CNT Composites

被引:22
|
作者
Peneva, Y. [1 ]
Valcheva, M. [1 ]
Minkova, L. [1 ]
Micusik, M. [2 ]
Omastova, M. [2 ]
机构
[1] Bulgarian Acad Sci, Inst Polymer, BU-1113 Sofia, Bulgaria
[2] Slovak Acad Sci, Inst Polymer, Bratislava 84236, Slovakia
来源
关键词
polypropylene nanocomposites; carbon nanotubes; nonisothermal crystallization kinetics; microhardness;
D O I
10.1080/00222340802403420
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The nonisothermal crystallization kinetics and microhardness of nanocomposites consisting of a polypropylene matrix (PP) and carbon nanotube filler (CNT) have been investigated. Three types of PP matrixes have been used: two of them are nonfunctionalized PP that differ slightly in their melt flow index, whereas the third is grafted with maleic anhydride (MA). Ozawa formalism has been used to study the nonisothermal crystallization kinetics. The results show that the CNT filler has a nucleation role in the nonisothermal crystallization of PP. For all nanocomposites, the nonisothermal crystallization rate increases up to 4% CNT and then decreases slightly or remains almost constant at the higher filler content. This fact has been interpreted in terms of an aggregation of the particles at high filler concentration, which leads to a decrease of the nucleation ability of the filler because the number of heterogeneous nuclei decreases. The crystallization mechanism of the PP matrixes almost does not change in the presence of the CNT filler. The microhardness of the two nonfunctionalized PP increases when the filler content increases and then remains constant above a certain filler content. The experimental microhardness values of the composites based on the functionalized PP are lower than those of the corresponding calculated additive values. The decrease of the creep constant with the filler addition is not significant, as should be expected when inorganic filler is added to a polymer matrix. This is due to the very fine dispersion of the fillers into the polymer matrix at the nanoscale level.
引用
收藏
页码:1197 / 1210
页数:14
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