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Synthesis and characterization of siliconized epoxy-1, 3-bis(maleimido)benzene intercrosslinked matrix materials

机译:硅化环氧-1,3-双(马来酰亚胺基)苯交联基质材料的合成与表征

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摘要

Intercrosslinked network of siliconized epoxy-1,3-bis(maleimido)benzene matrix systems have been developed. The siliconization of epoxy resin was carried out by using various percentages of (5-15%) hydroxyl-terminated polydimethylsiloxane (HTPDMS) with gamma -aminopropyltriethoxysilane (gamma -APS) as crosslinking agent and dibutyltindilaurate as catalyst. The siliconized epoxy systems were further modified with various percentages of (5-15%) 1,3-bis(maleimido)benzene (BMI) and cured by using diaminodiphenylmethane (DDM). The neat resin castings prepared were characterized for their mechanical properties. Mechanical studies indicate that the introduction of siloxane into epoxy resin improves the toughness of epoxy resin with reduction in the values of stress-strain properties whereas, incorporation of bismaleimide into epoxy resin improves stress-strain properties with lowering of toughness. However, the introduction of both siloxane and bismaleimide into epoxy resin influences the mechanical properties according to their percentage content. Differential scanning calorimetry (DSC), thermogravimetric analysis (TGA) and measurement of heat distortion temperature were also carried out to assess the thermal behavior of the matrix samples. DSC thermogram of the BMI modified epoxy systems show unimodel reaction exotherms. The glass transition temperature (T-g), thermal degradation temperature and heat distortion temperature of the cured BMI modified epoxy and siliconized epoxy systems increase with increasing BMI content and this may be due to the homopolymerization of BMI rather than Michael addition reaction. The morphology of the BMI modified epoxy and siliconized epoxy systems were also studied by scanning electron microscopy. (C) 2001 Elsevier Science Ltd. All rights reserved. [References: 31]
机译:已经开发出硅化的环氧-1,3-双(马来酰亚胺基)苯基质体系的交联网络。通过使用各种百分比的(5-15%)羟基封端的聚二甲基硅氧烷(HTPDMS),以γ-氨基丙基三乙氧基硅烷(γ-APS)为交联剂,以二月桂酸二丁基锡为催化剂进行环氧树脂的硅化。用各种百分比的(5-15%)1,3-双(马来酰亚胺基)苯(BMI)进一步修饰硅化的环氧体系,并使用二氨基二苯甲烷(DDM)进行固化。制备的纯净树脂铸件具有机械性能。力学研究表明,将硅氧烷引入环氧树脂可降低应力-应变性能值,从而提高了环氧树脂的韧性,而将双马来酰亚胺掺入环氧树脂可降低应力-韧性,从而提高了应力-应变性能。但是,将硅氧烷和双马来酰亚胺都引入环氧树脂中会影响其机械性能,具体取决于它们的百分比含量。还进行了差示扫描量热法(DSC),热重分析(TGA)和热变形温度的测量,以评估基质样品的热行为。 BMI改性环氧体系的DSC热分析图显示了单模反应放热。固化的BMI改性环氧树脂和硅化环氧体系的玻璃化转变温度(T-g),热降解温度和热变形温度随着BMI含量的增加而增加,这可能是由于BMI的均聚而不是迈克尔加成反应。还通过扫描电子显微镜研究了BMI改性环氧树脂和硅化环氧树脂体系的形态。 (C)2001 Elsevier ScienceLtd。保留所有权利。 [参考:31]

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