环氧树脂
材料科学
缩水甘油醚
热固性聚合物
复合材料
纳米纤维
纤维素
固化(化学)
动态力学分析
纳米复合材料
复合数
双酚A
聚合物
有机化学
化学
作者
Liang Yue,Fei Liu,Shekar Mekala,Ammar Patel,Richard A. Gross,Ica Manas‐Zloczower
标识
DOI:10.1021/acssuschemeng.8b06073
摘要
This work describes the preparation and characterization of biobased fiber reinforced resins using bacterial cellulose (BC) as the matrix reinforcing phase and diglycidyl ether diphenolate ethyl ester (DGEDP-ethyl) as the biobased epoxy resin. BC mats were prepared by static cultivation of strain Gluconacetobacter xylinus ATCC 700178 in Hestrin–Schramm medium augmented with mannitol in sterile containers. After freeze-drying, the surface of the BC matrix fibers was modified to introduce trimethylsilyl moieties (BCTMS). Reinforced by BCTMS nanofiber networks were fabricated by impregnation of BCTMS matrixes with the resin mixture followed by hot-pressing and curing. Resulting DGEDP-ethyl/BCTMS composites with 5, 10, 20, and 30%-by-vol BCTMS network loading were formed. The BC network proved effective in reinforcing the epoxy resin matrix. The composite Young's modulus (ET) increased from 1.22 ± 0.41 GPA for the neat DGEDP-ethyl thermoset to 8.8 ± 0.98 for the composite with 30%-by-vol BCTMS. Furthermore, the storage modulus (E′) increased for DGEDP-ethyl/30%BCTMS relative to the neat DGEDP-ethyl resin below Tg (30 °C) by 3-fold (2.27 to 7.7 GPA) and above Tg (180 °C) by 100-fold. This work highlights the potential to use prefabricated BC matrixes produced by microbial fermentation along with a biobased epoxy resin to provide high-performance biobased composites.
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