Thermal Spectroscopy and Kinetic Studies of PEO/PVDF Loaded by Carbon Nanotubes

L. Gaabour
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引用次数: 14

Abstract

Nanocomposites of polyethylene oxide (PEO) and polyvinylidene fluoride (PVDF) without and with low content of single and multiwalled carbon nanotubes (SWCNTs-MWCNTs) were prepared and studied by thermogravimetric analysis (TGA) using different heating rate. TGA results indicate that the thermal stability of neat PEO/PVDF blend was improved with both heating rate and incorporation of carbon nanotubes (CNTs). The degradation temperature for neat blend was lower than those of the nanocomposites after adding both SWCNTs and MWCNTs. As increase of heating rate, the onset of decomposition is irregularly moved to higher temperatures. This indicates that the thermal stability of the polymeric matrices has been improved after addition of CNTs. The residual weight of the samples left increased steadily with adding of both SWCNTs and MWCNTs. Kinetic thermodynamic parameters such as activation energy, enthalpy, entropy, and Gibbs free energy are evaluated from TGA data using Coats-Redfern model. The values of all parameters irregularly decrease with increasing of heating rate due to increasing of heating rate temperature, the random scission of macromolecule chain in the polymeric matrices predominates and the activation energy has a lower value.
碳纳米管负载PEO/PVDF的热光谱及动力学研究
制备了不含和低含量单壁和多壁碳纳米管(SWCNTs-MWCNTs)的聚乙烯氧化物(PEO)和聚偏氟乙烯(PVDF)纳米复合材料,并在不同升温速率下对其进行了热重分析(TGA)。TGA结果表明,随着升温速率和碳纳米管(CNTs)的加入,纯PEO/PVDF共混物的热稳定性得到改善。纯共混物的降解温度低于同时加入SWCNTs和MWCNTs的纳米复合材料的降解温度。随着升温速率的增加,分解的起始点不规则地向较高的温度移动。这说明加入CNTs后聚合物基体的热稳定性得到了改善。随着SWCNTs和MWCNTs的加入,样品的剩余重量稳步增加。利用Coats-Redfern模型对TGA数据进行了活化能、焓、熵和吉布斯自由能等动力学热力学参数的计算。由于升温速率温度的升高,各参数值随升温速率的增加而不规则降低,高分子基体中大分子链的随机断裂占主导地位,活化能值较低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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