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首页> 外文期刊>Journal of Applied Polymer Science >Preparation and characterizations of RTV epoxy blends using amide maleic anhydride-g-liquid polybutadience as both reactive toughening and curing components
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Preparation and characterizations of RTV epoxy blends using amide maleic anhydride-g-liquid polybutadience as both reactive toughening and curing components

机译:使用酰胺酸酐-G-液相用的RTV环氧树脂共混物的制备及表征作为反应增韧和固化组分

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摘要

Amide maleic anhydride-g-liquid polybutadience (AMALPB) was synthesized using maleic anhydride-g-liquid polybutadience (MALPB) with ethylenediamine (EDA), and its structure was confirmed by FTIR and 1 H-nuclear magnetic resonance spectra, respectively. It was then used as a reactive toughening agent to make blends with diglycidyl end-capped poly(bisphenol-A-co-epichlorohydrin epoxy cured at room temperature. Their thermal decomposing behaviors did not show much difference because both EDA and AMALPB possessed similar aliphatic groups. All their glass transition temperatures (T-g) increased more than 10 degrees C than that of the neat epoxy, and with the addition of AMALPB, the blends were greatly strengthened upon heating as show from their storage moduli. When AMALPB was added at 10 wt %, its elongation at break increases to a maximum of 8.8% which was about two times higher than that of the neat epoxy, and its tensile strength also increased. However, the excessive addition of AMALPB resulted in an apparent decline in their tensile strength at content above 20%. The simultaneous improvements in both tensile strength and strain were attributed to the existence of well-dispersed rubber particles in the continuous matrices performing plastic deformation that resulted from the chemical bonds of interfaces among the rubber particles and matrix, and meanwhile, inducing the deflection of the cracks. (C) 2017 Wiley Periodicals, Inc.
机译:使用与乙二胺(EDA)的马来酸酐-G-液体多乳酪细胞(MALPB)合成酰胺马来酸酐-G-液体多呋喃酸(AMALPB),其结构分别通过FTIR和1 H核磁共振谱证实其结构。然后用作反应性增韧剂,以使二缩水甘油末端封端的聚(双酚-A-共氯醇环氧树脂在室温下固化。它们的热分解行为没有显着差异,因为EDA和Amalpb都具有类似的脂肪族基团。所有玻璃化转变温度(Tg)比整齐环氧树脂的玻璃化转变温度(Tg)增加到10℃,并且随着Amalpb的添加,在加热时,随着储存模量的显示,混合物大大加强。当Amalpb加入10wt时%,其断裂伸长量增加至最大值为8.8%,大约比整齐的环氧树脂高出两倍,其拉伸强度也增加。然而,过量加入Amalpb在其拉伸强度下表现出明显的下降高于20%的内容。拉伸强度和菌株的同时改善归因于在连续矩阵中的井分散的橡胶颗粒存在由橡胶颗粒和基质之间的界面的化学键,且同时,引起裂缝的偏转,从而塑性变形。 (c)2017 Wiley期刊,Inc。

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