聚氨酯弹性体设计的若干准则

H. L. Spell, C. E. Macdonald, R. B. Turner
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引用次数: 1

摘要

考虑到组成、反应条件和加工过程中的众多变量,设计具有特定性能的聚氨酯弹性体确实是一项具有挑战性的任务。对热稳定性、韧性、疲劳和其他关键品质等特性的控制需要理论和实验知识的纲要。优化单一性能,例如,低温回弹性,可能需要改变成分,这可能会损害其他重要性能。因此,为了平衡整个系统以满足规范限制,需要的不仅仅是经验方法,而是在合理的时间内实现目标。在本次演讲中,我们将展示,通过使用一系列复杂的测试方法和精心设计的实验与计算机建模相结合,可以将分段弹性体的剪裁置于科学的基础上。表征的主要方法是动态力学光谱、小角x射线散射、电子显微镜、傅里叶变换红外和差示扫描量热法。特殊实验包括系统地合成和测试各种模型化合物。确定了最佳软段性能,如链长和迁移率。合成并表征了适当分离并具有高热完整性和机械完整性的硬段。这些和相关的实验使我们对弹性体力学和热行为的分子机制有了更好的了解。有了这些知识,我们可以在构建弹性体时选择分子成分和控制相关系,以满足最终使用要求,要求最大的静态和动态聚合物性能。
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Some criteria for the design of polyurethaneurea elastomers

Given the numerous variables in composition, reaction conditions, and processing, the design of a polyurethane elastomer with a specified set of properties is indeed a challenging task. The control of characteristics such as heat stability, toughness, fatigue, and other key qualities requires a compendium of theoretical and experimental knowledge. Optimizing a single property, e.g., low temperature resiliency, can necessitate changes in composition that may compromise other important properties. Thus, to balance the entire system in order to meet the specification limits, much more than an empirical approach is needed to achieve the goal in a reasonable time. In this presentation, we will demonstrate that, by use of an array of sophisticated testing methods and carefully designed experiments combined with computer modeling, the tailoring of a segmented elastomer can be placed on a scientific basis. Key methods of characterization are dynamic mechanical spectroscopy, small angle X-ray scattering, electron microscopy, Fourier transform infrared, and differential scanning calorimetry. Special experiments included the systematic synthesis and testing of a wide range of model compounds. Optimum soft segment properties such as chain length and mobility were defined. Hard segments that are properly segregated and have high thermal and mechanical integrity were synthesized and characterized. These and related experiments have led us to a better understanding of the molecular mechanisms underlying the mechanical and thermal behavior of an elastomer. With this knowledge we can select molecular components and control phase relationships in building elastomers to meet end use requirements that demand maximum static and dynamic polymer properties.

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