Relations Between the Aspect Ratio of Carbon Nanotubes and the Formation of Percolation Networks in Biodegradable Polylactide/Carbon Nanotube Composites

被引:154
作者
Wu, Defeng [1 ]
Wu, Liang [1 ]
Zhou, Weidong [2 ]
Sun, Yurong [1 ]
Zhang, Ming [1 ]
机构
[1] Yangzhou Univ, Sch Chem & Chem Engn, Yangzhou 225002, Jiangsu, Peoples R China
[2] Yangzhou Univ, Testing Ctr, Yangzhou 225002, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
aspect ratio; carbon nanotubes; composites; nanocomposites; percolation network; polylactide; rheology; RHEOLOGICAL BEHAVIOR; POLYMER NANOCOMPOSITES; ELECTRICAL-CONDUCTIVITY; MECHANICAL-PROPERTIES; POLY(ETHYLENE OXIDE); EPOXY NANOCOMPOSITES; FIBER SUSPENSIONS; SHEAR-FLOW; CRYSTALLIZATION; ORIENTATION;
D O I
10.1002/polb.21909
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 biodegradable polylactide composites containing carbon nanotubes (CNTs) with high aspect ratio (HAR) and low aspect ratio (LAR) were prepared by melt mixing. The physical properties of those two systems were characterized in terms of rheology, conductivity, and mechanical properties for establishing preliminary structure-property relations. Several viscoelastic models were then used to further describe the relations between aspect ratio and percolation network of CNTs. The results show that these two CNTs present different structural characteristics in the polylactide (PLA) matrix during melt mixing: the LAR CNTs are far stiffer than the HAR CNTs. At low loading levels, the former is dispersed as bent fibers or their small bundles, whereas the latter is dispersed as self-entangled flocs, presenting far larger hydrodynamic radius than the former. At high loading levels, both are dispersed as flocs due to strong tube-tube interactions. However, the two CNTs show approximate average floc size and mesh size because they present same rigid length and effective aspect ratio. At identical loadings, therefore, the HAR CNTs have more total number of flocs than that of the LAR CNTs, forming network with more compact structure and imparting higher contributions to properties of the composites as a result. (C) 2010 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 48: 479-489, 2010
引用
收藏
页码:479 / 489
页数:11
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