环氧树脂
材料科学
热稳定性
缩水甘油醚
复合材料
介孔二氧化硅
玻璃化转变
固化(化学)
双酚A
复合数
热重分析
超声
介孔材料
聚合物
填料(材料)
化学工程
化学
催化作用
有机化学
工程类
作者
Farzana Yeasmin,Abul K. Mallik,Adib H. Chisty,Fataha Nur Robel,Md. Shahruzzaman,Papia Haque,Mohammed Mizanur Rahman,Nanami Hano,Makoto Takafuji,Hirotaka Ihara
出处
期刊:Heliyon
[Elsevier]
日期:2021-01-01
卷期号:7 (1): e05959-e05959
被引量:40
标识
DOI:10.1016/j.heliyon.2021.e05959
摘要
For the first time, we incorporated mesoporous micro-silica (5 μm, pore size = 50 nm) as a filler in epoxy resin aiming to enter polymer into the pore of the silica. As expected, the thermal stability of the composite increased remarkably, followed by noteworthy thermal degradation kinetics when compared to the controlled cured epoxy resin. Composites were prepared by the direct dispersion of modified nano-silica, modified mesoporous micro-silica, unmodified mesoporous micro-silica, non-porous micro-silica, and irregular micro-silica of various pore sizes as fillers in diglycidyl ether of bisphenol-A epoxy resin via ultra-sonication and shear mixing, followed by oven-curing with 4,4-diaminodiphenyl sulfone. DSC and TGA analyses demonstrated a higher glass transition temperature (increased by 3.65–5.75 °C) and very high activation energy for thermal degradation (average increase = 46.2%) was obtained for the same unmodified silica composite compared to pure epoxy, respectively.
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