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High-temperature polyimide composites prepared from soluble polymeric and crosslinkable oligomeric precursors: phase demixing and properties

机译:由可溶的聚合物和可交联的低聚物前体制备的高温聚酰亚胺复合材料:相分离和性能

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Rigid/crosslinked flexible polyimide composites were prepared from soluble polymeric and oligomeric precursors: poly(4,4'-oxydiphenylene pyromellitamic acid) [PMDA-ODA(PAA)], poly(4,4'-oxydiphenylene pyromellitamic diethyl ester) [PMDA-ODA(ES)], acetylene-terminated isoimide oligomer of 3,3',4,4'-benzophenonetetracarboxylic dianhydride/1,3-bis(3-aminophenoxy)benzene (BTDA-APB) and acetylene-terminated imide oligomer of 2,2'-bis(3,4-dicarboxyphenyl)hexafluoropropane dianhydride/1,3-bis(3-aminophenoxy)benzene (6FDA-APB). PMDA-ODA(PAA) precursor was found to react with BTDA-APB isoimide oligomer in N-methyl-2-pyrollidone (NMP), resulting in gels. Furthermore, PMDA-ODA(PAA) exhibited a limited miscibility in making its homogeneous solution with 6FDA-APB imide oligomer in NMP, consequently leading to large domains in the softbaked blend films as well as in the resultant composite films. In contrast, for PMDA-ODA(ES) blends with 6FDA-APB and BTDA-APB, homogeneous ternary solutions with a relatively high solids content of less than or equal to 30 wt% were easily achieved in NMP over the entire composition range. Dried blend films were optically clear except a few compositions. For some compositions, the optical transparency in the dried films was retained through the thermal curing process, providing optically transparent semi-interpenatrating network (semi-IPN) composites. However, for the other compositions, phase separation took place through thermal curing, forming domains of submicrometre scales in the resultant composites. Properties of the polyimide composites were investigated by dynamic mechanical thermal analysis (d.m.t.a.), stress-strain analysis and self-adhesion measurement. In particular, the self-adhesion property of PMDA-ODA was significantly improved by the composite formation with 6FDA-APB, but not improved by the composite formation with BTDA-APB. The good self-adhesion in the PMDA-ODA/6FDA-APB composite was characterized by X-ray photoelectron spectroscopy and attributed mainly to the favourable molecular interdiffusion through the 6FDA-APB component segregated on the surface. In addition, the residual stress and relaxation behaviour were measured. (C) 1998 Elsevier Science Ltd. All rights reserved. [References: 28]
机译:刚性/交联的柔性聚酰亚胺复合材料是由可溶性聚合物和低聚物前体制备而成的:聚(4,4'-氧二苯并吡咯二酸)[PMDA-ODA(PAA)],聚(4,4'-氧二苯并吡咯二酸二乙酯)[PMDA- ODA(ES)],3,3',4,4'-二苯甲酮四羧酸二酐/ 1,3-双(3-氨基苯氧基)苯(BTDA-APB)的乙炔封端的异酰亚胺低聚物,以及2的乙炔封端的酰亚胺低聚物2'-双(3,4-二羧基苯基)六氟丙烷二酐/ 1,3-双(3-氨基苯氧基)苯(6FDA-APB)。发现PMDA-ODA(PAA)前体与N-甲基-2-吡咯烷酮(NMP)中的BTDA-APB异酰亚胺低聚物反应,形成凝胶。此外,PMDA-ODA(PAA)在NMP中与6FDA-APB酰亚胺低聚物形成均相溶液时,其混溶性有限,因此导致软烘烤共混膜以及所得复合膜中出现较大的畴。相反,对于PMDA-ODA(ES)与6FDA-APB和BTDA-APB的混合物,在整个组成范围内的NMP中,均很容易获得固含量低于或等于30 wt%的均相三元溶液。除少量组合物外,干燥的共混物薄膜光学透明。对于某些组合物,通过热固化过程保留了干燥膜中的光学透明性,从而提供了光学透明的半互穿网络(semi-IPN)复合材料。然而,对于其他组合物,通过热固化进行相分离,从而在所得复合物中形成亚微米级的区域。通过动态机械热分析(d.m.t.a.),应力应变分析和自粘测量来研究聚酰亚胺复合材料的性能。特别地,通过与6FDA-APB的复合物形成显着改善了PMDA-ODA的自粘性能,但是没有通过与BTDA-APB的复合物形成而改善。通过X射线光电子能谱表征了PMDA-ODA / 6FDA-APB复合材料中良好的自粘合性,这主要归因于通过表面上分离的6FDA-APB组分的有利分子相互扩散。另外,测量了残余应力和松弛行为。 (C)1998 Elsevier ScienceLtd。保留所有权利。 [参考:28]

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