Structure characteristics and thermal properties of silane-grafted-polyethylene/clay nanocomposite prepared by reactive extrusion

被引:77
作者
Lu, Hongdian
Hu, Yuan [1 ]
Li, Ming
Chen, Zuyao
Fan, Weicheng
机构
[1] Univ Sci & Technol China, State Key Lab Fire Sci, Hefei 230026, Anhui, Peoples R China
[2] Univ Sci & Technol China, Dept Chem, Hefei 230026, Anhui, Peoples R China
基金
中国国家自然科学基金; 高等学校博士学科点专项科研基金;
关键词
polyethylene; nanocomposite; montmorillonite; silane; graft;
D O I
10.1016/j.compscitech.2006.01.018
中图分类号
TB33 [复合材料];
学科分类号
摘要
Silane-grafted-polyethylene/OMT nanocomposite (VTMS-g-PE/OMT) was prepared by reactive extrusion from linear low density polyethylene (LLDPE), vinyltrimethoxysilane (VTMS), organically modified montmorillonite (OMT) and dicumyl peroxide (DCP). A series of tests such as X-ray diffraction (XRD), transmission electron microscopy (TEM), Fourier transfer infrared (FTIR) and thermogravimetric analysis (TGA) have been performed to characterize the morphology and thermal properties of the graft polymer and its nanocomposite. Results show that the graft polymer (VTMS-g-PE) chains have been successfully intercalated into OMT layers proved by XRD data (a d-spacing of 3.4 nm) and TEM images; the PE chains have been chemically bounded to the OMT layers proved by FTIR spectra; the nanocomposite exhibits a higher thermal-oxidative stability than that of either the VTMS-grafted-LLDPE or the LLDPE proved by TGA curves. The increase in thermal properties lies in two facts: one is the formation of chemical bonds between PE macromolecules and OMT layers during silane graft reaction; the other is the in situ graft of PE macromolecules onto the OMT surfaces during thermal-oxidative degradation. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3035 / 3039
页数:5
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