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MXD6/PA6/EPT共混物的相容性研究

Study on compatibility of MXD6/PA6/EPT blends
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摘要 以马来酸酐接枝乙烯丙烯热塑性弹性体(EPT-g-MAH)为反应性增容剂,通过熔融共混方法制得聚间苯二甲胺己二酸/聚酰胺6/乙烯丙烯热塑性弹性体(MXD6/PA6/EPT)共混物。采用Molau实验、动态流变仪、扫描电子显微镜、傅里叶变换红外光谱仪和红外近红外成像系统等分析研究了EPT的分散性能以及MXD6/PA6/EPT共混物的流变性能和形态结构。实验结果表明,PA6与EPT-g-MAH发生原位化学反应生成的EPTb-PA6嵌段共聚物是增容MXD6/EPT共混体系的根本原因;MXD6/PA6/EPT/EPT-g-MAH共混体系的储能模量(G′)、损耗模量(G″)以及复数粘度(η)均高于MXD6/PA6/EPT共混体系,且在低频区增加幅度更为明显;EPT-g-MAH的引入导致共混体系的相分离温度升高、时温叠加频率适用范围增大;EPT-g-MAH的引入增强了EPT与MXD6界面相互作用,分散相EPT在MXD6基体中分散更加均匀、尺寸明显减小。 In this paper,poly(m-xylene adipamide)/polyamide 6/ethylene propylene terpolymer(MXD6/PA6/EPT)blends were obtained by melt blending method,and EPT grafted maleic anhydride (MAH)was used as a reactive compatibilizer in this process.The dispersion performance of EPT and rheological property,morpho-logical structure of MXD6/PA6/EPT blends were studied by Molau test,dynamic rheometer,scanning electron microscopy,FT-IR spectrometer and infrared near infrared imaging system.The experimental results showed that EPT-b-PA6 block copolymer was the root cause of compatibilizing MXD6/EPT blend system,which was generated by PA6 and EPT-g-MAH through situ chemical reaction.The energy storage modulus (G′),loss modulus (G″)and complex viscosity (η)of MXD6/PA6/EPT/EPT-g-MAH blend system were higher than MXD6/PA6/EPT blend system’s,and increased more obviously in low frequency area.The introduction of EPT-g-MAH improved phase separation temperature,broadened the scope of applications of time temperature super-position frequency and enhanced interface interaction between EPT and MXD6.Meanwhile,the dispersed phase EPT dispersed more evenly in MXD6 matrix and its size reduced significantly.
出处 《功能材料》 EI CAS CSCD 北大核心 2016年第10期10101-10106,共6页 Journal of Functional Materials
基金 黑龙江省教育厅科学技术研究资助项目(12511588) 黑龙江省研究生创新科研资助项目(YJSCX2011-204HLJ)
关键词 聚间苯二甲胺己二酸 乙烯丙烯热塑性弹性体 共混物 相容性 poly(m-xylene adipamide) ethylene propylene terpolymer blend compatibility
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  • 1刘喜军,朱文明,姜兆华,祁颖.聚丙烯接枝衣康酸增容PA6/PP共混物性能及形态研究[J].中国塑料,2007,21(1):18-24. 被引量:5
  • 2Ferry J. D.. Viscoelastic Properties of Polymers, 3rd Ed.[M], New York: John Wiley & Sons, 1980: 56
  • 3Masuda T., Takahashi M.. Kobunshi[J], 1993, 42: 734-738
  • 4Wu S. H.. Polymer[J], 1987, 28: 1 144-1 148
  • 5Cowie J. M. G., Elexpuru E. M.. Eur. Polym. J.[J], 1992, 28(6): 623-626
  • 6Peng M., Zheng Q.. Chinese J. Polym. Sci.[J], 2000, 18(6): 565-568
  • 7Wisniiwsky C., Marin G., Monge P.. Eur. Polym J.[J], 1984, 20: 691-696
  • 8Colby R. H.. Polymer[J], 1989, 30: 1 275-1 278
  • 9Brekner M. J., Cantow H. J., Schmider H. A.. Polym. Bull.[J], 1985, 14: 17-24
  • 10Han C. D., Kim J. K.. Macromolecules[J], 1989, 22: 4 292-4 302

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