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首页> 外文期刊>Journal of Applied Polymer Science >Effect of polymeric additives on properties of glass-bisphenol A dicyanate laminate composites
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Effect of polymeric additives on properties of glass-bisphenol A dicyanate laminate composites

机译:聚合物添加剂对玻璃双酚A二氰酸酯层压复合材料性能的影响

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The polycyanurate network matrix derived from the thermal, dibutyl tin dilaurate catalyzed polymerization of bisphenol A dicyanate was modified in their glass-laminate composites with different linear polymeric additives bearing pendant phenol, cyanate, and epoxy functions. The mechanical properties and fracture energy for delamination of the glass-laminate composites were estimated as functions of the backbone structure and concentration of the various additives. The effect of altering the nature or concentration of the functional group for a given backbone structure of the additive was examined in some cases. Except for the epoxy functional acrylic polymer, all other systems adversely affected the fracture energy for delamination of the composites due to either plasticization or embrittlement of the matrix. With the exception of the styrene-hydroxyphenyl maleimide (SPM) copolymer, the other modifiers impaired the mechanical properties and adversely affected the thermomechanical profile of the composites. In the cases of the phenol functional acrylic polymer and its cyanate derivative, plasticization of the matrix by the partly phase-separated additive, which eased the fiber debonding, appears to be responsible for the impairment of the mechanical properties. The high glass transition temperature SPM copolymer enhanced the resin-reinforcement interaction through dipolar interactions induced by the hydroxyl groups, which resulted in amelioration of the mechanical properties. However, its possible coreaction and formation of a brittle, homogeneous phase with the polycyanurate was conducive for poor damage tolerance. The SEM analysis of the fractured composites showed that in the elastomers fiber debonding is the major cause for delamination. Although the presence of SPM led to a stronger interphase, failure occurred either in the brittle matrix or through fiber breakage. (C) 2000 John Wiley & Sons, Inc. [References: 37]
机译:由双月桂酸二丁锡热催化双酚A二氰酸酯聚合得到的聚氰尿酸酯网络基质在其玻璃层压复合材料中进行了改性,使用了具有线性酚醛,氰酸酯和环氧官能团的线性添加剂。估计玻璃层压复合材料分层的机械性能和断裂能,取决于骨架结构和各种添加剂的浓度。在某些情况下,研究了给定添加剂骨架结构改变官能团的性质或浓度的影响。除环氧官能丙烯酸类聚合物外,所有其他系统均会由于基质的增塑或脆化而对复合材料分层产生的断裂能产生不利影响。除苯乙烯-羟苯基马来酰亚胺(SPM)共聚物外,其他改性剂会损害机械性能并不利地影响复合材料的热机械性能。在酚官能丙烯酸类聚合物及其氰酸酯衍生物的情况下,部分相分离的添加剂对基质的增塑作用(其易于纤维脱粘)似乎是造成机械性能下降的原因。高玻璃化转变温度的SPM共聚物通过羟基诱导的偶极相互作用增强了树脂-增强相互作用,从而改善了机械性能。然而,其可能的共作用以及与聚氰尿酸酯形成脆性,均匀的相有利于较差的损伤耐受性。断裂复合材料的SEM分析表明,在弹性体中,纤维剥离是分层的主要原因。尽管SPM的存在会导致更强的相间结合,但无论是在脆性基质中还是通过纤维断裂都会发生破坏。 (C)2000 John Wiley&Sons,Inc. [参考:37]

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