Blending Polyurethane Thermosets Using Dynamic Urethane Exchange

聚氨酯 热固性聚合物 弹性体 挤压 压缩成型 聚合物 动态力学分析 造型(装饰) 材料科学 压缩永久变形 混溶性 单体 相(物质) 聚酯纤维 化学 复合材料 有机化学 模具 天然橡胶
作者
Jeremy L. Swartz,Daylan T. Sheppard,Greg Haugstad,William R. Dichtel
出处
期刊:Macromolecules [American Chemical Society]
卷期号:54 (23): 11126-11133 被引量:33
标识
DOI:10.1021/acs.macromol.1c01910
摘要

Recycling crosslinked polyurethanes (PUs) is accomplished through mechanical or chemical processes that are energy-intensive or produce plastics of lesser value. Polymer recycling processes are notably intolerant of polymer mixtures, yet the ability to reprocess and compatibilize two or more crosslinked PUs together will make this process more amenable to mixed waste streams while offering an opportunity to tune the properties of the recycled polymer products. Here, we blend a rigid polyester PU and a soft polyether PU using twin-screw extrusion to yield materials with tunable mechanical properties based on the feed composition. Their material properties were compared to those of compression-molded reprocessed blends and blends where the monomers were mixed prior to synthesis. The extruded materials showed similar mechanical and thermal properties to newly prepared blends and had higher-value mechanical properties compared to the samples reprocessed via compression molding. The morphologies of the blends were observed using phase imaging via atomic force microscopy to show that there is less phase separation in the extruded materials compared to compression-molded blends. The mechanical properties of these materials were tunable from soft to elastomeric to rigid based on the feed composition, and this tunability was demonstrated through four consecutive reprocessing cycles, through which the mechanical properties were steadily varied from rigid to soft by incorporating increasing amounts of soft polyether PU material. This blending method for reprocessing mixed waste compatibilizes different PUs and provides a means to tune the mechanical properties of a PU product, even if starting from waste streams of varying compositions. As such, this process represents an intriguing new approach for polymer reprocessing.
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