Morphology and Thermal Properties of Maleic Anhydride Grafted Polypropylene/Ethylene-Vinyl Acetate Copolymer/Wood Powder Blend Composites

被引:23
作者
Dikobe, Dorine Geneth [1 ]
Luyt, Adriaan Stephanus [1 ]
机构
[1] Univ Free State, Dept Chem, ZA-9866 Phuthaditjhaba, South Africa
基金
新加坡国家研究基金会;
关键词
blends; calorimetry; composites; fibers; poly(propylene) (PP); MECHANICAL-PROPERTIES; TEREPHTHALATE BLENDS; SISAL FIBER; CRYSTALLIZATION; EVA; PP; COCRYSTALLIZATION; NANOCOMPOSITES; POLYETHYLENE; DSC;
D O I
10.1002/app.31630
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Maleic anhydride grafted polypropylene (MAPP) was blended with ethylene vinyl acetate (EVA) copolymer to form MAPP/EVA polymer blends. Wood powder (WP) was mixed into these blends at different weight fractions to form MAPP/EVA/WP blend composites. Differential scanning calorimetry (DSC) analysis of the blends showed small melting peaks between those of EVA and MAPP, which indicated interaction and cocrystallization of fractions of EVA and MAPP. The presence of MAPP influenced the EVA crystallization behavior, whereas the MAPP crystallization was not affected by the presence of EVA. Scanning electron microscopy, Fourier transform infrared spectroscopy, and DSC results show that the WP particles in the MAPP/EVA blend were in contact with both the MAPP and EVA phases and that there seemed to be chemical interaction between the different functional groups. This influenced the crystallization behavior, especially of the MAPP phase. The thermogravimetric analysis results show that the MAPP/EVA blend had two degradation steps. An increase in the WP content in the blend composite led to an increase in the onset of the second degradation step but a decrease in onset of the first degradation step. The presence of WP in the blend led to an increase in the modulus but had almost no influence on the tensile strength of the blend. The dynamic mechanical analysis results confirm the interaction between EVA and MAPP and show that the presence of WP only slightly influenced the dynamic mechanical properties. (C) 2010 Wiley Periodicals, Inc. J Appl Polym Sci 116: 3193-3201, 2010
引用
收藏
页码:3193 / 3201
页数:9
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