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Determining soft segment structure-property effects in the enhancement of segmented polyurethane performance

机译:确定软段结构 - 性能对增强分段聚氨酯性能的影响

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摘要

Liquid Crystalline Elastomer (LCE)-inspired segmented polyurethane elastomers possessing widely different extents of ordering were created to mimic the hierarchical structure of the continuous matrix and superior mechanical performance of spider silk fibers. The silk's remarkable toughness originates from a fiber morphology that possesses [beta]-pleated crystalline sheets within an amorphous matrix. In the polyurethane materials, various extents of poly(ethylene oxide) (PEO) soft segment ordering were implemented within continuous soft domains that were connected by hexamethylene diisocyanate-butanediol (HDI-BDO) hard segments. Soft segment crystallinity studies revealed the need to optimize the extent of continuous soft domain ordering. Highly crystalline PEO soft segments, while they display good microphase segregation properties, sacrifice extensibility due to their high melting transition temperature. Moderately crystalline PEO soft segments, meanwhile, possess less defined phase segregation but enhanced mechanical properties from their reversible dispersed crystalline soft segment domains. Non-crystalline Pluronic copolymer systems had good mechanical properties that resulted from both a strong hard segment incompatibility and a highly mobile soft segment matrix. Hydrogen-bonded hard domain shearing during in-situ tensile deformation yields oriented hard blocks that align at a preferred tilt angle of ±60° from the strain direction. Extensive alignment and orientation of the moderately-ordered PEO soft segments occurred during deformation, which was consistent with its observed mechanical behavior. Pluronic-containing segmented polyurethanes formed an ordered mesophase in the continuous soft matrix during deformation. A series of cyclic, aliphatic polyurethanes with dicyclohexyl methane diisocyanate (HMDI) hard segments and poly(tetramethylene oxide) (PTMO) soft segments was synthesized to study compositional effects on the extent of soft segment mixing, and how these effects translated to both mechanical and barrier performance. Shorter soft segment chain systems displayed a greater hard segment compatibility, which resulted in materials that were both more rigid mechanically and provided better barrier characteristics.
机译:创建具有广泛不同顺序程度的液晶弹性体(LCE)启发的分段聚氨酯弹性体,以模仿连续基质的分层结构和蜘蛛丝纤维的优异机械性能。丝的显着韧性源自纤维形态,该纤维形态在无定形基质内具有β-折叠的结晶片。在聚氨酯材料中,在通过六亚甲基二异氰酸酯-丁二醇(HDI-BDO)硬链段连接的连续软域内,实现了不同程度的聚环氧乙烷(PEO)软链段排序。软段结晶度研究表明需要优化连续的软结构域有序程度。高度结晶的PEO软链段虽然表现出良好的微相偏析特性,但由于其较高的熔融转变温度而牺牲了延展性。同时,中等结晶度的PEO软链段具有较少定义的相偏析,但由于其可逆的分散结晶软链段域而具有增强的机械性能。非结晶的Pluronic共聚物体系具有良好的机械性能,这是由于强烈的硬链段不相容性和高度移动的软链段基质所致。在原位拉伸变形过程中,氢键结合的硬区剪切会产生定向的硬块,这些硬块与应变方向的倾斜角度优选为±60°。在变形过程中发生了中等顺序的PEO软段的广泛对准和定向,这与其观察到的机械行为一致。含Pluronic的嵌段聚氨酯在变形过程中在连续的软基质中形成有序的中间相。合成了一系列具有二环己基甲烷二异氰酸酯(HMDI)硬链段和聚环氧丙烷(PTMO)软链段的环状脂肪族聚氨酯,以研究软链段混合程度的组成影响,以及这些作用如何转化为机械和屏障性能。较短的软链段链系统显示出更大的硬链段兼容性,这导致材料在机械上更加坚硬并且具有更好的阻隔特性。

著录项

  • 作者

    Waletzko Ryan Scott;

  • 作者单位
  • 年度 2009
  • 总页数
  • 原文格式 PDF
  • 正文语种 eng
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