首页> 外文期刊>Colloid and polymer science >Diglycidyl ether of bisphenol-A epoxy resin-polyether sulfone/polyether sulfone ether ketone blends:phase morphology,fracture toughness and thermo-mechanical properties
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Diglycidyl ether of bisphenol-A epoxy resin-polyether sulfone/polyether sulfone ether ketone blends:phase morphology,fracture toughness and thermo-mechanical properties

机译:双酚A环氧树脂的二缩水甘油醚-聚醚砜/聚醚砜醚酮共混物:相形态,断裂韧性和热机械性能

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摘要

The properties of diglycidyl ether of bisphenol-A epoxy resin toughened with poly(ether sulfone ether ketone)(PESEK)and poly(ether sulfone)(PES)polymers were investigated.PESEK was synthesised by the nucleophilic substitution reaction of 4,4'-difluorobenzophenone with dihydroxydiphenylsuifone using sulfolane as solvent and potassium carbonate as catalyst at 230 deg C.The T_g-composition behaviour of the homogeneous epoxy resin/PESEK blend was modelled using Fox,Gordon-Taylor and Kelley-Bueche equations.A single relaxation near the glass transition of epoxy resin was observed in all the blend systems.From dynamic mechanical analysis,the crosslink density of the blends was found to decrease with increase in the thermoplastic concentration.The storage modulus of the epoxy/PESEK blends was lower than that of neat resin,whilst it is higher for epoxy/PES blends up to glass transition temperature,thereafter it decreases.Scanning electron microscopic studies of the blends revealed a homogeneous morphology.The homogeneity of the blends was attributed to the similarity in chemical structure of the modifier and the cured epoxy network and due to the H-bonding interactions between the blend components.The fracture toughness of epoxy resin increased on blending with PESEK and PES.The increase in fracture toughness was due to the increase in ductility of the matrix.The thermal stability of the blends was comparable to that of neat epoxy resin.
机译:研究了用聚醚砜醚酮(PESEK)和聚醚砜(PES)聚合物增韧的双酚A环氧树脂的二缩水甘油醚的性能。通过4,4'-的亲核取代反应合成了PESEK二氟二苯甲酮与二羟基二苯甲酮,以环丁砜为溶剂,碳酸钾为催化剂,温度为230℃。使用Fox,Gordon-Taylor和Kelley-Bueche方程模拟了均相环氧树脂/ PESEK共混物的T_g组成行为。在所有共混体系中均观察到环氧树脂的转变。通过动态力学分析发现,共混物的交联密度随热塑性浓度的增加而降低。环氧/ PESEK共混物的储能模量低于纯树脂,直到环氧/ PES共混物在玻璃化转变温度以下时较高,然后降低。环氧共混物的扫描电子显微镜研究显示其均质性共混物的均匀性归因于改性剂的化学结构和固化的环氧网络的相似性,以及共混物组分之间的氢键相互作用。与PESEK和PES共混时,环氧树脂的断裂韧性增加断裂韧性的增加归因于基体的延展性的提高。共混物的热稳定性与纯环氧树脂相当。

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