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Curing Mechanism of Condensed Polynuclear Aromatic Resin and Thermal Stability of Cured Resin

机译:缩合多环芳烃树脂的固化机理及固化后的树脂的热稳定性

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In order to improve the thermal stability of condensed polynuclear aromatic (COPNA) resin synthesized from vacuum residue, 1,4-benzenedimethanol was added to cure COPNA resin. The curing mechanism was investigated by pro-ton nuclear magnetic resonance spectrometry, solid carbon-13 nuclear magnetic resonance spectrometry and Fourier trans-form infrared spectroscopy. Microstructures of the uncured and the cured COPNA resins were studied by scanning electron microscopy and X-ray diffractometry. The thermal stability of COPNA resins before and after curing was tested by thermo-gravimetric analysis. The element composition of the cured COPNA resin heated at different temperatures was analyzed by an element analyzer. The results showed that the uncured COPNA resin reacted with the cross-linking agent during the cur-ing process, and the curing mechanism was conifrmed to be the electrophilic substitution reaction. Compared with the un-cured COPNA resin, the cured COPNA resin had a smooth surface, well-ordered and streamlined sheet structure with more crystalline solids, better molecular arrangement and orientation. The weight loss process of the uncured and cured COPNA resins was divided into three stages. Carbon residue of the cured COPNA resin was 41.65%at 600℃, which was much higher than 25.02%of the uncured COPNA resin, which indicated that the cured COPNA resin had higher thermal stability.
机译:为了提高由真空残渣合成的缩合多核芳烃(COPNA)树脂的热稳定性,添加1,4-苯二甲醇以固化COPNA树脂。通过质子核磁共振波谱,固体碳13核磁共振波谱和傅立叶变换红外光谱对固化机理进行了研究。通过扫描电子显微镜和X射线衍射法研究未固化和固化的COPNA树脂的微观结构。通过热重分析测试了COPNA树脂在固化前后的热稳定性。通过元素分析仪分析在不同温度下加热的固化COPNA树脂的元素组成。结果表明,未固化的COPNA树脂在固化过程中与交联剂反应,固化机理为亲电取代反应。与未固化的COPNA树脂相比,固化后的COPNA树脂具有光滑的表面,井井有条的流线型片状结构,具有更多的结晶固体,更好的分子排列和取向。未固化和固化的COPNA树脂的失重过程分为三个阶段。固化的COPNA树脂在600℃时的碳残留率为41.65%,远高于未固化的COPNA树脂的25.02%,这表明固化的COPNA树脂具有较高的热稳定性。

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    College of Chemical Engineering, State Key Laboratory of Heavy 0il Processing, China University of Petroleum, Qingdao 266580;

    College of Chemical Engineering, State Key Laboratory of Heavy 0il Processing, China University of Petroleum, Qingdao 266580;

    College of Chemical Engineering, State Key Laboratory of Heavy 0il Processing, China University of Petroleum, Qingdao 266580;

    College of Chemical Engineering, State Key Laboratory of Heavy 0il Processing, China University of Petroleum, Qingdao 266580;

    College of Chemical Engineering, State Key Laboratory of Heavy 0il Processing, China University of Petroleum, Qingdao 266580;

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