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Poly(furfuryl alcohol) bioresin-modified LY5210 epoxy thermosets

机译:聚(糠醇)生物蛋白改性LY5210环氧热固性件

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摘要

This study deals with the preparation of bio-based epoxy blends and of their mechanical, thermal, and morphological characterization. Thus, the commercial tetra-functional epoxy resin, LY5210, and various weight fractions of poly(furfuryl alcohol), PFA, were subjected into curing reaction by employing diethylenetriamine (DETA) as a curing agent. Mechanical properties of the intact resin as well as the epoxy-PFA blends have been explored to show the influence of the incorporated PFA on the epoxy matrix. Dynamic mechanical thermal analysis (DMTA) revealed that the blends had slightly lower storage modulus than that of the neat epoxy. Interestingly, in tensile analysis, epoxy-PFA blends exhibited higher elastic modulus and lower toughness values. Surface study of the modified samples was characterized by scanning electron microscopy (SEM), and morphological results confirmed the mechanical analyses results. Finally, the adhesion properties of resultant blends have been evaluated by subjecting them on to steel substrate and obtained results were correlated to mechanical properties. Generally, the results suggested the replacement of fossil-resourced epoxy resin with the PFA bio-based resin up to 25wt% with negligible effect on mechanical and thermal properties. This achievement is important because the bioresin moieties may favor the environmental degradation of the thermoset network.
机译:本研究涉及制备生物基环氧树脂和它们的机械,热和形态学特性。因此,通过使用二亚乙基三胺(DETA)作为固化剂,对聚(糠醇),PFA的商业四官能环氧树脂,LY5210和各种重量分数进行固化反应。已经探讨了完整树脂的机械性能以及环氧-PFA共混物,以显示掺入的PFA对环氧基质的影响。动态机械热分析(DMTA)显示共混物的储存量略低于整齐的环氧树脂。有趣的是,在拉伸分析中,环氧-PFA共混物表现出更高的弹性模量和较低的韧性值。通过扫描电子显微镜(SEM)表征改性样品的表面研究,并且形态结果证实了机械分析结果。最后,通过对它们进行钢基材进行了所得共混物的粘合性能,得到的结果与机械性能相关。通常,结果表明,将化石资源的环氧树脂与PFA生物基树脂的替代为25wt%,对机械和热性能的效果可忽略不计。这种成就很重要,因为嗜虫蛋白部分可能有利于热固性网络的环境劣化。

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