材料科学
共聚物
环氧树脂
抗弯强度
极限抗拉强度
玻璃化转变
复合材料
艾氏冲击强度试验
固化(化学)
脆性
硅氧烷
聚合物
作者
Lele Liu,Fan Wang,Yaping Zhu,Huimin Qi
标识
DOI:10.1177/09540083221125862
摘要
Previous studies on linear epoxy (bisphenol A epoxy) resin/benzoxazine composites showed that with the addition of epoxy (EP) resin, the resulting copolymers exhibited an increased glass transition temperature ( T g ) ( T g reached a maximum value at a specific content), improved flexural strength, lower heat resistance, and reduced tensile strength. Herein, branched EP resin (AG-80)/benzoxazine copolymers featuring novolac (N-box) and siloxane (Si-box) chains were prepared without any external curing agent. In both systems, the EP resin endowed the copolymers with an increased crosslinking density; however, T g continued to increase with increasing EP content. In addition, the heat resistance of the copolymers gradually enhanced. Different types of benzoxazines have various effects on the properties of copolymers. In terms of mechanical properties, AG-80/N-box copolymers exhibited brittle fracture characteristics; with increasing EP content, the flexural strength of the copolymer decreased while the tensile strength increased. AG-80/Si-box copolymers exhibited ductile fracture characteristics, with gradual increases in flexural and tensile strengths. Furthermore, with increasing EP content, the molecular chain migration ability and network homogeneity of the AG-80/N-box copolymers decreased gradually. Alternatively, in the case of the AG-80/Si-box copolymers, the molecular chain migration ability remained unchanged and network homogeneity improved. Hence, the developed copolymers can be used as resin matrices for the fabrication of advanced composites.
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