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DDM-PMDA-HAB噁唑酰亚胺共聚物的合成及其耐热性

Preparation and Heat-Resistance of DDM-PMDA-HAB Benzoxazole-Imide Copolymers

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【作者】 高原张茂根王炳祥沈健

【Author】 GAO Yuan~(a,b),ZHANG Mao-Gen~(a,b*),WANG Bing-Xiang~(a,b),SHEN Jian~(a,b,c)(~aSchool of Chemistry and Environmental Science,Nanjing Normal University,Nanjing 210097;~bJiangsu Provincial Engineering Research Center of Biomedical Functional Materials,Nanjing;~cResearch Center of Surface and Interface Chemistry and Engineering Technology,Nanjing University,Nanjing)

【机构】 南京师范大学化学与环境科学学院南京师范大学化学与环境科学学院 南京210097江苏省生物医药功能材料工程研究中心南京南京210097南京大学表面和界面化学工程技术研究中心南京

【摘要】 用4,4′-二氨基二苯基甲烷(DDM),3,3′-二羟基联苯胺(HAB),与均苯四甲酸二酐(PMDA)在N,N-二甲基乙酰胺中室温缩聚,制备了3种共聚酰胺酸(CPAA);CPAA膜经热处理失水环化,形成共聚酰亚胺(CPI);在N2气下经500℃热处理,重排转变为DDM-PMDA-HAB唑酰亚胺共聚物(CPB I)。ATR光谱显示了CPI和CPB I膜的特征结构。TGA分析佐证了唑化转变。CPB I膜均显示优良的耐热性(用质量损失5%时的温度Td表示),比相应的CPI高93~138℃;比二元聚合物PMDA-HAB聚苯并唑(PBO)高65~86℃。廉价的DDM在二胺单体中所占摩尔分数为75%时,CPB I仍保持优良的耐热性(Td为573℃)。

【Abstract】 Three poly(amic acid) copolymers(CPAAs) were synthesized from 4,4′-diamino diphenyl(methane)(DDM),3,3′-dihydroxy-4,4′-diamino-biphenyl(HAB) and pyromellitic dianhydride(PMDA) by condensation in N,N-dimethylacetamide at room temperature.Thermal cyclodehydration of CPAA cast films led to the formation of copolyimides(CPIs),which were rearranged to DDM-PMDA-HAB benzoxazole-imide(copolymers)(CPBIs) by further thermal treatment at 500 ℃ under nitrogen.ATR spectra showed the charac-(teristic) structure of CPIs and CPBIs.TGA analysis confirmed the rearrangement to the formation of Polybenzoxazoles(PBOs).All the CPBI films displayed excellent thermal stability,shown by T_d,the temperature at which the mass loss of the polymer is 5%.T_d values of CPBI films are 93~138 ℃ higher than that of corresponding CPIs,and 65~86 ℃ higher than that of PMDA-HAB PBO.The molar ratio of cheap DDM among diamines can increase up to 75%,while the CPBIs still have the excellent heat resistance(T_d is 573 ℃).

【基金】 上海伊曼纺织化工有限公司资助(南京师范大学211090B423)
  • 【文献出处】 应用化学 ,Chinese Journal of Applied Chemistry , 编辑部邮箱 ,2006年09期
  • 【分类号】O633.5
  • 【被引频次】2
  • 【下载频次】106
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