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Epoxy resin containing the poly(sily ether): Preparation, morphology, and mechanical properties

机译:含聚(甲醚)的环氧树脂:制备,形态和机械性能

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The poly(sily ether) with pendant chloromethyl groups (PSE) was synthesized by the polyaddition of dichloromethylsilane (DCM) and diglycidylether of bisphenol A (DGEBA) with tetrabutylammonium chloride (TBAC) as a catalyst. This polymer was miscible with diglycidyl ether of bisphenol A (DGEBA), the precursor of epoxy resin. The miscibility is considered to be due mainly to entropy contribution because the molecular weight of DGEBA is quite low. The blends of epoxy resin with PSE were prepared through in situ curing reaction of diglycidyl ether of bisphenol A (DGEBA) and 4,4'-diaminodiphenylmethane (DDM) in the presence of PSE. The DDM-cured epoxy resin/PSE blends with PSE content up to 40 wt % were obtained. The reaction started from the initial homogeneous ternary mixture of DGEBA/DDM/PSE. With curing proceeding, phase separation induced by polymerization occurred. PSE was immiscible with the 4,4'-diaminodiphenylmethane-cured epoxy resin (ER) because the blends exhibited two separate glass transition temperatures (T(g)s) as revealed by the means of differential scanning calorimetry (DSC) and dynamic mechanical analysis (DMA). SEM showed that all the ER/PSE blends are heterogeneous. Depending on blend composition, the blends can display PSE- or epoxy-dispersed morphologies, respectively. The mechanical test showed that the DDM-cured ER/PSE blend containing 25 wt % PSE displayed a substantial improvement in Izod impact strength, i.e., epoxy resin was significantly toughened. The improvement in impact toughness corresponded to the formation of PSE-dispersed phase structure. (C) 2003 Wiley Periodicals, Inc. [References: 36]
机译:通过将二氯甲基硅烷(DCM)和双酚A的二缩水甘油醚(DGEBA)与四丁基氯化铵(TBAC)进行加聚反应,合成了具有氯甲基侧基(PSE)的聚(甲醚)。该聚合物与环氧树脂的前体双酚A的二缩水甘油醚(DGEBA)可混溶。由于DGEBA的分子量非常低,因此认为混溶性主要是由于熵的贡献。环氧树脂与PSE的共混物是在PSE存在下,通过双酚A的二缩水甘油醚(DGEBA)与4,4'-二氨基二苯甲烷(DDM)的原位固化反应制备的。获得了具有高达40wt%的PSE含量的DDM固化的环氧树脂/ PSE共混物。该反应从DGEBA / DDM / PSE的初始均匀三元混合物开始。随着固化的进行,发生了由聚合引起的相分离。 PSE与4,4'-二氨基二苯基甲烷固化的环氧树脂(ER)不混溶,因为通过差示扫描量热法(DSC)和动态力学分析表明,共混物表现出两个独立的玻璃化转变温度(T(g)s)。 (DMA)。 SEM显示,所有ER / PSE共混物都是异质的。根据共混物的组成,共混物可以分别显示PSE或环氧分散的形态。机械测试表明,含有25wt%PSE的DDM固化的ER / PSE共混物显示出悬臂梁式冲击强度的显着改善,即,环氧树脂被显着增韧。冲击韧性的提高对应于PSE分散相结构的形成。 (C)2003 Wiley Periodicals,Inc. [参考:36]

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