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首页> 外文期刊>Polymer Engineering and Science >Cure Kinetics, Phase Behaviors, and Fracture Properties of Bismaleimide Resin Toughened by Poly(phthalazinone ether ketone)
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Cure Kinetics, Phase Behaviors, and Fracture Properties of Bismaleimide Resin Toughened by Poly(phthalazinone ether ketone)

机译:聚酞嗪酮醚酮增韧双马来酰亚胺树脂的固化动力学,相行为和断裂性能

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摘要

Poly(phthalazinone ether ketone)s (PPEK) were used to toughen bismaleimide (BMI) resin composed of 4,4'-bismaleimidodiphenyl methane (BMDM) and O,O'-diallyl bisphenyl A (DABPA). Dynamic differential scanning calorimetry (DSC) of the blends was carried out for kinetic analysis of the curing reaction. The reaction activation energy indicated that the reaction mechanism remained the same even after the incorporation of PPEK. The reaction-induced phase separation process in BMI/PPEK blends was investigated by optical microscopy (OM). The primary phase structure of the blends was fixed at the early stage of phase separation, and a secondary phase separation was observed as a result of the high viscosity of the blends. Scanning electron microscope (SEM) graphs showed that the morphology of the cured resin changed from a dispersed structure to a phase-inverted structure with the increase of PPEK content. Compared with the neat resin, the fracture toughness of the modified resin exhibits a moderate increase when PPEK was incorporated. Several toughening mechanisms, such as local plastic deformation, crack deflection, and branches, presumably took part in improving the toughness of BMI/PPEK blends on the basis of the morphology. [PUBLICATION ABSTRACT]
机译:聚(酞嗪酮醚酮)(PPEK)用于增韧由4,4'-双马来酰亚胺二苯甲烷(BMDM)和O,O'-二烯丙基双苯基A(DABPA)组成的双马来酰亚胺(BMI)树脂。进行共混物的动态差示扫描量热法(DSC)以用于固化反应的动力学分析。反应活化能表明,即使加入PPEK,反应机理仍保持相同。通过光学显微镜(OM)研究了BMI / PPEK共混物中反应诱导的相分离过程。共混物的初级相结构固定在相分离的早期,由于共混物的高粘度,观察到次级相分离。扫描电子显微镜(SEM)图表明,随着PPEK含量的增加,固化树脂的形态从分散结构变为相变结构。与纯树脂相比,当掺入PPEK时,改性树脂的断裂韧性适度提高。几种增韧机制,例如局部塑性变形,裂纹变形和分支,据推测参与了基于形态的BMI / PPEK共混物韧性的提高。 [出版物摘要]

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    《Polymer Engineering and Science 》 |2009年第12期| p.2301-2308| 共8页
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    Yongjin Han, Gongxiong Liao, Yajuan Xu, Guipeng Yu, Xigao JianDepartment of Polymer Science and Materials, Dalian University of Technology, Dalian 116012, ChinaCorrespondence to: Gongxiong Liao, e-mail: liaogongxiong@dl.cn or Xigao Jian, e-mail: jian4616@dl.cnContract grant sponsor: The National Natural Science Foundation of China, contract grant number: 50703004.DOI 10.1002/pen.21453Published online in Wiley InterScience (www.interscience.wiley.com).© 2009 Society of Plastics Engineers,;

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