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HIGH-PERFORMANCE UV-CURABLE URETHANE ACRYLATES VIA DEBLOCKING CHEMISTRY

机译:高性能的可紫外固化的脲烷丙烯酸酯,具有去块化学作用

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Research in urethane-acrylate UV-curables has shown that these materials have mechanical properties inferior to those of thermoplastic polyurethanes with very similar composition owing to the high cross-link density in UV-curables; in particular, their ultimate extension is low (less than 100%). Past attempts at increasing the ultimate extension involved com promising the advantages of the UV-curing process. In this work, thermally labile bonds were made and then broken after curing, so as to incorporate thermoplastic polyurethane in the UV-cured polymer. This method achieved the desired improvement in ultimate properties without compromising the advantages of the UV-curing process. Two different reactive diluents and three different chain extenders were utilized, keeping the soft segment type (PPO), hard segment type (IPDI), and their weight fractions constant. The resulting polymers were similar to interpenetrating networks of linear or cross-linked polyurethanes and linear or cross-linked polyacrylates with properties entirely different from their UV-cured precursors, as well as the corresponding polyurethanes. All the materials involved were characterized by tensile testing and dynamic mechanical analysis. The ultimate extensions as well as the ultimate strength of the final polymers were found to be significantly greater than those of the corresponding UV-curable precursors, while the degree of phase separation was found to have changed. The differences in mechanical properties of the UV curables and the polyurethanes cannot be explained in terms of differences in cross-link density or composition and are probably due to differences in their morphology. (C) 1996 John Wiley & Sons, Inc. [References: 15]
机译:氨基甲酸酯丙烯酸酯紫外线固化剂的研究表明,由于紫外线固化剂的交联密度高,这些材料的机械性能不如组成非常相似的热塑性聚氨酯。特别是,它们的最终延伸率很低(小于100%)。过去增加最终延伸率的尝试都涉及到紫外线固化工艺的优点。在这项工作中,进行了热不稳定键,然后在固化后将其破坏,以便将热塑性聚氨酯掺入UV固化的聚合物中。该方法在不损害紫外线固化工艺优势的前提下,在最终性能方面实现了所需的改进。使用两种不同的反应性稀释剂和三种不同的扩链剂,以保持软链段类型(PPO),硬链段类型(IPDI)及其重量分数恒定。所得的聚合物类似于线性或交联的聚氨酯和线性或交联的聚丙烯酸酯的互穿网络,其性质完全不同于其UV固化的前体以及相应的聚氨酯。通过拉伸测试和动态力学分析来表征所有涉及的材料。发现最终聚合物的极限延伸率和极限强度明显大于相应的UV可固化前体的极限延伸率和极限强度,而发现相分离的程度已改变。 UV固化剂和聚氨酯的机械性能差异无法用交联密度或组成的差异来解释,而可能是由于它们形态的差异。 (C)1996 John Wiley&Sons,Inc. [参考:15]

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