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Uralkyd and Poly(Butyl Methacrylate) Interpenetrating Polymer Networks

机译:聚氨酯和聚甲基丙烯酸丁酯互穿聚合物网络

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摘要

Hydroxy terminated alkyds synthesized from castor oil, glycerol, and different dibasic acids were used to develop uralkyds and their interpenetrating polymer networks (IPNs) with polybutyl methacrylate (PBMA). Glass transition temperature measurements give the evidence of interpenetration. The IPNs were characterized for their physicomechanical properties and their phase morphology was studied by scanning electron microscopy (SEM) and differential scanning calorimetry (DSC). As the concentration of the uralkyd in IPNs increases, a gradual increase in elongation, density, and swelling with a consequent decrease in the hardness were observed for all IPNS. Swelling is relatively more prominent in methyl ethyl ketone (MEK) and toluene than in water. From SEM it was observed that IPNs of PBMA-uralkyd containing phthalic anhydride (UA-P) as an acid part showed greater compatibility than those containing dimethyl terephthalate (UA-D). From thermogravimetric analysis (TGA) no significant change was observed in the degradation behavior of the IPNs.
机译:由蓖麻油,甘油和不同的二元酸合成的羟基封端的醇酸树脂用于开发醇酸树脂及其与聚甲基丙烯酸丁酯(PBMA)互穿的聚合物网络(IPN)。玻璃化转变温度的测量提供了互穿的证据。对IPN的物理力学性质进行了表征,并通过扫描电子显微镜(SEM)和差示扫描量热法(DSC)研究了它们的相形态。随着IPN中的缩果胶浓度增加,对于所有IPNS,观察到伸长率,密度和膨胀逐渐增加,从而导致硬度降低。甲基乙基酮(MEK)和甲苯中的溶胀相对比水更明显。从SEM观察到,含有邻苯二甲酸酐(UA-P)作为酸部分的PBMA-缩醛烷基醇的IPN显示出比含有对苯二甲酸二甲酯(UA-D)的IPN更大的相容性。根据热重分析(TGA),未观察到IPN的降解行为发生重大变化。

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