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基于2,3,3',4'-二苯醚四甲酸二酐可溶性聚酰亚胺的亚胺化方法

Imidization Method on Soluble Polyimide Based on 2,3,3',4'-Diphenyl Ether Tetracarboxylic Acid Dianhydride
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摘要 采用2,3,3',4'-二苯醚四甲酸二酐(α-ODPA)与柔性二胺单体1,3-二(4-氨基苯氧基)苯(1,3,4-APB)合成了可溶性聚酰亚胺,其在N,N-二甲基乙酰胺(DMAc)、N-甲基吡咯烷酮(NMP)等极性溶剂中的溶解性得到提高,研究了亚胺化方法对基于α-ODPA的可溶性聚酰亚胺性能的影响和作用机制。结果表明,亚胺化方法对相对分子质量的影响是产生各项性能变化的根本原因,基于α-ODPA的聚酰亚胺适用于化学亚胺化方法,采用化学亚胺化方法能够得到的可溶性聚酰亚胺的数均相对分子质量为2. 68×10~4,5%热分解温度(T_(d5))为544. 7℃,玻璃化转变温度(T_g)为236. 1℃,热稳定性能良好。化学亚胺化聚酰亚胺树脂的拉伸强度为99. 99 MPa,冲击强度为102. 51 kJ/m^2,韧性性能优异。 The soluble polyimide was synthesized with 2,3,3', 4-diphenyl ether tetracarboxylic acid dianhydride (a-ODPA) and flexible diamine 1,3-bis(4'aminophenoxyl) benzene ( 1,3,4-APB), which enhanced the solubility of the polyimide in polar solvents such as N, N-dimethyl acetamide (DMAc) and N-methyl pyrrolidone(NMP). The effects and mechanism of action on the soluble polyimide based on a-ODPA were studied through imidization methods. The results show that the influence of imidization methods on molecular weight is the root cause of various performance changes. The chemical imidization method is suitable for the polyimide based on a-ODPA. The average molecular weight of the soluble polyimide obtained by the chemical imidization method is 2. 678 ~ 104. 5 % thermal decomposition temperature Td5 is 544.7 *C and glass transition temperature is 236.1 *t2, revealing the good thermal stability l The tensile strength of chemical imidized polyimide is 99.99 MPa, and the impact strength is 102.51 kJ/ m2, which shows excellent toughness.
作者 孙劲松 张朋 包建文 钟翔屿 张代军 Jinsong Sun', Peng Zhang, Jianwen Bao, Xiangyu Zhong, Daijun Zhang(1. School of Material Science and Engineering, Beijing Institute of Fashion Technology, Beijing 100029, China ; 2. AVIC Composite Technology Center, National Key Laboratory of Advanced Composites, Beijing 101300, China)
出处 《高分子材料科学与工程》 EI CAS CSCD 北大核心 2018年第9期5-11,共7页 Polymer Materials Science & Engineering
关键词 可溶性聚酰亚胺 化学亚胺化 热亚胺化 相对分子质量 力学性能 soluble polyimide chemical imidization thermal imidization molecular weight mechanical properties
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  • 1程茹,朱梦冰,黄培.热和化学亚胺化对ODPA/ODA聚酰亚胺薄膜性能的影响[J].材料工程,2007,35(7):51-54. 被引量:8
  • 2Kim I C,Kim J H,Lee K H,et al.Preparation of soluble polyimides and ultrafiltration membrane performances[J].Journal of Applied Polymer Science,2000,1(75):1-9.
  • 3Eichstadt A E,Ward T C,Bagwell M D,et al.Synthesis and characterization of amorphous partially aliphatic polyimide copolymers based on bisphenol-A dianhydrides[J].Macromolecules,2002,20(35):7561-7568.
  • 4Lu Q H,Yin J,Xu H J,et al.Preparation and properties of organo-soluble polyimides based-on 4,4'-diamino-3,3'-dimethyldipheylmethane and conventional dianhydrides[J].Journal of Applied Polymer Science,1999,10(72):1299-1304.
  • 5Ayala D,Lozano A E,Abajo J D,et al.Synthesis and characterization of novel polyimides with bulky pendant groups[J].Journal of Applied Polymer Science:Part A:Polymer Chemistry,1999,6(37):805-814.
  • 6Li F,Fang S W,Ge J J,et al.Diamine architecture effects on glass transitions,relaxation processes and other material properties in organo-soluble aromatic polyimide films[J].Polymer,1999,16(40):4571-4583.
  • 7Yen C T,Chen W C,Liaw D J,et al.Synthesis and properties of new polyimide-silica hybrid films through both intrachain and interchain bonding[J].Polymer,2003,23(44):7079-7087.
  • 8Banihashemi A,Abdolmaleki A.Novel aromatic polyimides derived from benzofuro[2,3-b]benzofuran-2,3,8,9-tetracarboxylic dianhydride (BBTDA)[J].European Polymer Journa1,2004,8(40):1629-1635.
  • 9Chen B K,Tsai Y J,Tsay S Y.2,6-Diamino-4-phenylphenol(DAPP)Copolymerized polyimides:synthesis and characterization[J].Polymer International,2006,1(55):93-100.
  • 10Chen H,Yin J.Synthesis and characterization of hyperbranched polyimides with good organosolubility and thermal properties based on a new triamine and conventional dianhydrides[J].Journal of Polymer Science:Part A:Polymer Chemistry,2002,21(40):3804-3814.

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