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Study on the catalytic prepolymerization of an acetylene-functional benzoxazine and the thermal degradation of its cured product

机译:乙炔基苯并恶嗪的催化预聚合及其固化产物的热降解研究

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摘要

In this paper, the prepolymerization of acetylene-functional benzoxazine was carried out by using nickel acetylacetonate hydrate/triphenyl phosphine as a catalyst at a low temperature. By this method, the reaction heat of acetylene polymerization was partially released and no ring-opening polymerization of benzoxazine occurred. After that, the prepolymer was cured stepwise to obtain the cured product according to a traditional curing process. As a comparison, another cured product was directly obtained from acetylene-functional benzoxazine by the traditional method without prepolymerization. The curing behaviors and the thermal properties of these two polybenzoxazines were investigated and compared by FTIR, DSC, DMA, and TGA. Their thermal decomposition behaviors were further studied by TGA-FTIR, Py-GC/MS, and SEM. The results show that the catalytic prepolymeriztion makes the whole curing process milder and more controllable in a broader processing window. Furthermore, more crosslinked-polyacetylene structures and benzene from the catalytic prepolymerization improve the thermal stability of the polybenzoxazines. Additionally, less amine compounds were detected in the prepolymerization system during the thermal decomposition process and the appearance of the residue was stable and controllable after pyrolysis.
机译:本文以乙酰丙酮镍水合物/三苯基膦为催化剂,在低温下进行了乙炔官能苯并恶嗪的预聚合。通过这种方法,部分释放了乙炔聚合反应的反应热,并且没有发生苯并恶嗪的开环聚合。之后,将预聚物逐步固化,以按照传统的固化方法获得固化产物。作为比较,通过乙炔官能的苯并恶嗪通过传统方法直接得到另一种固化产物,而没有预聚合。通过FTIR,DSC,DMA和TGA研究和比较了这两种聚苯并恶嗪的固化行为和热性能。通过TGA-FTIR,Py-GC / MS和SEM进一步研究了它们的热分解行为。结果表明,催化预聚合使整个固化过程更温和,更可控,且加工范围更广。此外,来自催化预聚合的更多的交联的聚乙炔结构和苯改善了聚苯并恶嗪的热稳定性。另外,在热分解过程中,在预聚合体系中检测到的胺化合物较少,并且热解后残留物的外观稳定且可控。

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