详细信息
Thermal curing reaction and heat-resistance of methyl-di(M-ethynylphenyl-amino)silane ( SCI-EXPANDED收录 EI收录)
文献类型:期刊文献
英文题名:Thermal curing reaction and heat-resistance of methyl-di(M-ethynylphenyl-amino)silane
作者:Song, Ning[1];Xu, Fang[1];Ni, Lizhong[1];Chen, Jianding[1]
机构:[1]E China Univ Sci & Technol, Sch Mat Sci & Engn, Minist Educ, Key Lab Special Funct Polymer Mat & Related Techn, Shanghai 200237, Peoples R China
年份:2012
卷号:126
期号:4
起止页码:1484
外文期刊名:JOURNAL OF APPLIED POLYMER SCIENCE
收录:;EI(收录号:20123215312860);WOS:【SCI-EXPANDED(收录号:WOS:000307005300034)】;
语种:英文
外文关键词:high temperature materials; thermal properties; curing of polymers; pyrolysis
摘要:Methyl-di(m-ethynylphenyl-amino)silane (MEAS) is a new kind of silazane with ethynylphenyl groups in the end of the molecule. The studies about the curing reaction kinetics and curing reaction mechanism are important for its application and performance. In this article, differential scanning calorimeter was used to study the curing reaction kinetics of MEAS. The results showed that both of the apparent activation energy (Ea) and the reaction order (n) that were evaluated with the method of Kissinger (113.4 kJ/mol, 0.93) agreed well with those using the method of Ozawa (116.1 kJ/mol, 0.95). According to structural changes during curing characterized using Fourier-transform infrared spectra, it was inferred that MEAS resin underwent the main four kinds of cross-linking reaction under the condition of heating. Thermogravimetric analysis was used to characterize the heat-resistance of MEAS thermoset. The results showed that the temperature of 5% weight loss based on the initial weight (Td5) of the thermoset was 632.4 degrees C and the residue yield at 900 degrees C was 86.4% in nitrogen. The thermoset sintered at 1450 degrees C in argon transformed into a ceramic with yield of 71%, which was studied by scanning electron microscopy and X-ray diffraction. The sintered products were smooth and hard solid and its chemical composition was made up of beta-SiC, a-Si3N4 ceramic and free carbon. (c) 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012
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