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Waterborne Polyimides and Poly(imide-Siloxane)s

机译:水性聚酰亚胺和聚(酰亚胺-硅氧烷)

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The optimum design for composite fiber matrix interfaces has not been established. Our working hypothesis is that the interfacial material should be: ductile, applicable from water, and either miscible with, or reactive with the matrix. Our focus has been to prepare water soluble Ultem poly(amic acid) salts for use as sizing and interface toughening materials for composite manufacturing. Stable water soluble Ultem type poly(amic acid) salts were prepared from methanolic tripropylamine. Rapid imidization (10 min at 260°C) of the poly(amic acid)s and poly(amic acid) salts allows for on-line processing. Epoxy/polyimide networks prepared from amine terminated Ultem polyimides and DER 331 epoxy resin showed microphase separation (100-300 nm inclusions) using transmission electron microscopy and atomic force microscopy. Diffusion of the reactive interface material was seen in the AFM of the polyimide/epoxy bilayer film, whereas no diffusion was evident in the poly(imide-siloxane) bilayer films.
机译:尚未确定复合纤维基质界面的最佳设计。我们的工作假设是,界面材料应:易延展,可从水中使用,并且可与基质混溶或反应。我们的重点是制备水溶性Ultem聚(酰胺酸)盐,以用作复合材料制造中的施胶剂和界面增韧材料。由甲醇三丙胺制备稳定的水溶性Ultem型聚(酰胺酸)盐。聚(酰胺酸)和聚(酰胺酸)盐的快速酰亚胺化(在260°C下10分钟)可以进行在线处理。由胺封端的Ultem聚酰亚胺和DER 331环氧树脂制备的环氧/聚酰亚胺网络通过透射电子显微镜和原子力显微镜显示出微相分离(夹杂物为100-300 nm)。在聚酰亚胺/环氧双层膜的AFM中观察到反应性界面材料的扩散,而在聚(酰亚胺-硅氧烷)双层膜中没有明显的扩散。

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