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尼龙-6 18的晶型转变研究
  • 期刊名称:高等学校化学学报, 2006, 27, 389.
  • 时间:0
  • 分类:O631.1[理学—高分子化学;理学—化学]
  • 作者机构:[1]上海交通大学化学化工学院,上海200240
  • 相关基金:国家自然科学基金(批准号:20274024,50233030)资助.
  • 相关项目:反应性超支化聚合物的设计、制备及其应用研究
中文摘要:

以偶偶尼龙-6 18为例,通过示差扫描量热分析(DSC)、广角X射线衍射(WAXD)与傅里叶变换红外光谱(FTOR)等方法研究了其Brill转变的过程,探索了脂肪族聚酰胺的晶型转变的本质.X射线衍射结果表明,随着温度的升高,尼龙-6 18由三斜晶系转变为假六方晶型,同时其DSC曲线上出现一个较宽的吸热峰.红外光谱结果表明,在其晶型转变过程中,晶体内氢键强度逐渐减弱,与酰胺键相连的C—C和C—N键发生扭曲.酰胺基团之间的亚甲基链段的振动逐渐增强,部分亚甲基单元由反式构象变成旁式构象,最后整齐排列的亚甲基链段逐渐变得无序化.

英文摘要:

The Brill transition of even-even nylon-6 18 was investigated by using differential scanning calorimetry( DSC ), temperature-dependent wide angle X-ray diffraction (WAXD) and Fourier transform infrared (FTIR). The X-ray diffraction results indicate that the melt-crystallized sample of nylon-6 18 transforms from the triclinic unit cell to the pseudo-hexagonal phase in the temperature range of 120-180℃. In this range, the thermograph of nylon-6 18 presents a broad endothermal peak. From the FTIR spectra, it can be found that, during the transition process of nylon-6 18, the intensity of the intrasheet hydrogen bonds becomes weak. At the same time, the CH2-amide bonds twist and the all-tram conformation of methylene sequences is disordered by inserting the gauche conformation. The CH2 segments are in a mobile state because of the enhanced stretching and twisting vibrations of C-CO and C-N bonds.

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