Thermal degradation kinetics of poly(methylvinylsilylene-co-styrene)

被引:4
作者
Devapal, D
Packirisamy, S [1 ]
Ambadas, G
Radhakrishnan, TS
Krishnan, K
Ninan, KN
机构
[1] Vikram Sarabhai Space Ctr, Polymers & Special Chem Div, Trivandrum 695022, Kerala, India
[2] Vikram Sarabhai Space Ctr, Analyt & Spect Div, Trivandrum 695022, Kerala, India
[3] Vikram Sarabhai Space Ctr, PCM Ent, Propellant & Special Chem Grp, Trivandrum 695022, Kerala, India
关键词
polysilahydrocarbon; poly(methylvinylsilylene-co-styrene); thermal degradation kinetics;
D O I
10.1016/S0040-6031(03)00355-1
中图分类号
O414.1 [热力学];
学科分类号
摘要
Thermal degradation kinetics of poly(methylvinylsilylene-co-styrene) copolymers, viz., PMVSS-I to PMVSS-V obtained by reacting methylvinyldichlorosilane (MVDCS) and styrene in 1:0.25, 1:0.5, 1:1, 1:3 and 1:7 mole ratios under dechlorination conditions, using sodium, was studied by thermogravimetry. The homopolymer, poly(methylvinylsilane) (PMVS), synthesized from MVDCS using sodium was also subjected to the above study for comparative evaluation. The kinetic parameters for thermal degradation, viz., activation energy (E) and pre-exponential factor (A) for the above polymers were estimated by non-isothermal kinetic methods such as Mac Callum-Tanner (M-T), Horowitz-Metzger (H-M), Madhusudhanan-Krishnan-Ninan (MKN) and Coats-Redfern (C-R). The order for thermal degradation of PMVS was found to be almost 0. In the case of the copolymers, the order was 1 for PMVSS-I and 2 for PMVSS-II to PMVSS-V. The observed difference in the order for thermal degradation of PMVSS-I when compared to the other copolymers is attributed to the presence of polysilyl linkages in PMVSS-I. It was found that the activation energy and pre-exponential factor showed an increase in trend with increase in concentration of styrene in the copolymer system. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:151 / 156
页数:6
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