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Synthesis and characterization of 1,1-bis(3-methyl-4-cyanatophenyl) cyclohexane - Epoxy - Bismaleimide matrices

机译:1,1-双(3-甲基-4-氰基苯基)环己烷-环氧-双马来酰亚胺基体的合成与表征

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摘要

A new cyanate ester monomer,1,1 -bis(3-methyl-4-cyanatophenyl) cyclohexane has been synthesized and characterized. Epoxy modified with 4, 8 and 12% (by wt) of cyanate ester were made using epoxy resin and 1,1-bis(3-methyl-4-cyanatophenyl) cyclohexane and cured by using diaminodiphenylmethane. The cyanate ester modified epoxy matrix systems were further modified with 4, 8 and 12% (by wt) of bismaleimide (N, N'-bismaleimido-4,4'-diphenyl methane). The formation of oxazolidinone and isocyanurate during cure reaction of epoxy and cyanate ester blend was confirmed by IR spectral studies. Bismaleimide-cyanate ester-epoxy matrices were characterized using differential scanning calorimetry (DSC), thermogravimetric analysis (TGA) and heat deflection temperature (HDT) analysis. The matrices, in the form of castings, were characterized for their mechanical properties; namely tensile strength, flexural strength and unnotched Izod impact test as per ASTM methods. Mechanical studies indicate that the introduction of cyanate ester (CE) into epoxy resin improves the toughness and flexural strength with reduction in tensile strength and glass transition temperature, whereas the incorporation of bismaleimide (BMI) into epoxy resin enhances the mechanical and thermal properties according to its percentage content. However, the introduction of both CE and BMI enhances the values of thermo-mechanical properties according to their percentage content. DSC thermogram of cyanate ester modified epoxy and BMI-modified epoxy show an unimodal reaction exotherms. The thermal degradation temperature and heat distortion temperature of the cured BMI-modified epoxy and CE-epoxy systems were increased with increasing BMI content. The morphology of the BMI modified epoxy and CE-epoxy systems were also studied by scanning electron microscope.
机译:合成并表征了一种新型的氰酸酯单体,1,1-双(3-甲基-4-氰基苯基)环己烷。用环氧树脂和1,1-双(3-甲基-4-氰基苯基)环己烷制备用4、8和12%(重量)氰酸酯改性的环氧树脂,并用二氨基二苯甲烷固化。用4、8和12%(重量)的双马来酰亚胺(N,N'-双马来酰亚胺基-4,4'-二苯基甲烷)进一步改性氰酸酯改性的环氧基质体系。红外光谱研究证实了环氧和氰酸酯共混物固化反应过程中恶唑烷酮和异氰脲酸酯的形成。使用差示扫描量热法(DSC),热重分析(TGA)和热变形温度(HDT)分析对双马来酰亚胺-氰酸酯-环氧树脂基质进行表征。以铸件形式的基体的机械性能经过了表征。即按照ASTM方法进行拉伸强度,弯曲强度和无缺口悬臂梁式冲击试验。力学研究表明,将氰酸酯(CE)引入环氧树脂可提高韧性和弯曲强度,同时降低拉伸强度和玻璃化转变温度,而双马来酰亚胺(BMI)掺入环氧树脂则可提高机械性能和热性能。其百分比含量。但是,CE和BMI的引入根据其百分比含量提高了热机械性能的值。氰酸酯改性的环氧树脂和BMI改性的环氧树脂的DSC热分析图显示出单峰反应放热。随着BMI含量的增加,固化的BMI改性的环氧树脂和CE-环氧体系的热降解温度和热变形温度也随之增加。还通过扫描电子显微镜研究了BMI改性的环氧树脂和CE-环氧体系的形态。

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