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Engineered polysaccharide alpha-1,3 glucan asisocyanate-reactivecomponent in viscoelastic polyurethane foams

机译:在粘弹性聚氨酯泡沫中的工程多糖α-1,3葡聚糖籽氰酸酯 - 反弹

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摘要

Enzymatic polymerization is emerging as scalable method to convert sucrose to engineered polysaccharides. Polymer architecture and material properties can be controlled selectively to produce novel differentiated biomaterials. One first example for such an engineered polysaccharide is alpha-1,3-polyglucose (alpha-1,3-glucan) synthesized using glucosyltransferase (GTF) enzymes. Stable dispersions of alpha-1,3-glucan in polyether polyols were prepared with narrow particle size distributions, which are reactive with isocyanate allowing for covalent bonding to the hard segment of the polyurethane polymer matrix. This study further explored the use of alpha-1,3-glucan (PS) in the preparation of viscoelastics (VE) polyurethane foams. The introduction of alpha-1,3-glucan into the polyurethane polymer matrix was found to increase the load-bearing properties of VE foams without impacting the density. Other key performance properties of VE foams were effectively unchanged, including resilience, tensile, and tear strength. Cell size and morphology were also unaffected. The glass transition of these VE foams was not impacted; however, the overall thermal dimensional stability was improved as considerable reduction in compression set was observed. The results of this study indicated that alpha-1,3-glucan disperses in polyether polyols to improve performance characteristics of the VE foams, as well as other flexible polyurethane foams properties.
机译:酶聚合是一种将蔗糖转化为工程多糖的可扩展方法。聚合物的结构和材料性能可以被选择性地控制,以生产新型的差异化生物材料。这种工程多糖的第一个例子是使用葡萄糖基转移酶(GTF)酶合成的α-1,3-聚葡萄糖(α-1,3-葡聚糖)。在聚醚多元醇中制备了α-1,3-葡聚糖的稳定分散体,其粒径分布窄,与异氰酸酯反应,从而与聚氨酯聚合物基质的硬段共价键合。本研究进一步探索了α-1,3-葡聚糖(PS)在制备粘弹性(VE)聚氨酯泡沫中的应用。在聚氨酯聚合物基体中引入α-1,3-葡聚糖可以提高VE泡沫的承载性能,而不会影响密度。VE泡沫塑料的其他关键性能基本不变,包括回弹性、拉伸强度和撕裂强度。细胞大小和形态也不受影响。这些VE泡沫的玻璃化转变没有受到影响;然而,随着压缩永久变形的显著降低,整体热尺寸稳定性得到改善。本研究结果表明,α-1,3-葡聚糖分散在聚醚多元醇中,以改善VE泡沫的性能特征,以及其他柔性聚氨酯泡沫的性能。

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