Thermal stability and lifetime estimates of a high temperature epoxy by Tg reduction

被引:24
作者
Anderson, Benjamin J. [1 ]
机构
[1] Sandia Natl Labs, Mat Sci & Engn Ctr, Albuquerque, NM 87185 USA
基金
美国能源部;
关键词
Epoxy; Degradation; Thermal aging; Lifetime; GLASS-TRANSITION TEMPERATURE; NON-ARRHENIUS BEHAVIOR; DEGRADATION; PREDICTION; POLYMERS; KINETICS; OXIDATION; RESINS;
D O I
10.1016/j.polymdegradstab.2013.08.001
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Thermal degradation of a high temperature epoxy network is studied in terms glass transition temperature (T-g) reduction over a temperature window encompassing the T-g of the network. The T-g is shown to decrease as the network is thermally aged at elevated temperatures in air and in argon. The duration of the aging experiments is extended to long time such that the absolute T-g reduction approaches a long time reduction plateau. Degradation is dominated by non-oxidative pyrolysis with a small contribution from diffusion limited thermal oxidative degradation at the surface. A time-temperature superposition is constructed from the extent of T-g reduction of samples aged in air and the thermal shift factors are shown to have Arrhenius scaling behavior. An activation energy is extracted that agrees with previous activation energy measurements derived from other property measurements of the same network aged under similar conditions. The agreement of the activation energy with past results shows that T-g reduction is controlled by the same degradation mechanism and may be used as an observable for lifetime estimates when thermal degradation is pyrolytic in nature. The extent of T-g reduction is modeled with an autocatalytic rate expression and compared to previous property measurements to show the difference in sensitivity of observable material properties on degradation. (C) 2013 Elsevier Ltd. All rights reserved.
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页码:2375 / 2382
页数:8
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