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Biocompatible nanocomposites based on semi-interpenetrating polymer networks and nanosilica modified by bioactive amino acid tryptophan: Morphology, dynamics and properties

机译:基于半互相聚合物网络和通过生物活性氨基酸色氨酸改性的生物相容性纳米复合材料:形态,动力学和性能

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摘要

The nanocomposites based on polyurethane and poly(2-hydroxyethyl methacrylate) (PU-PHEMA) semi-IPN matrices with 17 or 37 wt.% PHEMA, containing from 3 to 15 wt.% nanosilica (NS), were synthesized aiming at the biomedical applications. NS surface was modified using the mechanosorptive method, with formation of basically monomolecular layer of biologically active substance - amino acid tryptophan. The AFM analysis of morphology of the nanocomposites and the complex DSC-TSDC-DMA-CRS analysis of their thermal, relaxation and elastic properties over the broad temperature range, from - 150 to 200 degrees C, were performed. Satisfactory nanofiller dispersion and the pronounced changes in matrix morphology were observed at 17 wt.% PHEMA in the matrix, whereas nanofiller submicro- and microaggregates prevailed in the nanocomposites with 37 wt.% PHEMA. As a result, just in the first case the most substantial "constrained dynamics" effect (e.g., increasing T-g by 20-30 degrees C) was observed in the nanocomposites.
机译:基于聚氨酯和聚(2-羟乙基甲基丙烯酸甲酯)(PU-PHEMA)半IPN基质的纳米复合材料,其具有17或37重量%的PHEMA,含有3-15重量%的PHEMA,含有3-15重量%。%纳米硅(NS),旨在瞄准生物医学应用程序。使用机械装饰方法改变NS表面,形成基本上单分子的生物活性物质 - 氨基酸色氨酸层。进行AFM分析纳米复合材料的形态和复合DSC-TSDC-DMA-CRS在宽温度范围内的热,弛豫和弹性性能的分析,从-150至200℃下进行。在17重量%中观察到令人满意的纳米填充分散和基质形态的显着变化。基质中的%phema,而纳米填充物亚亚胚状物和微烧结在纳米复合材料中具有37重量%。%phema。结果,在第一种情况下,在纳米复合材料中观察到最重要的“约束动态”效应(例如,增加20-30℃)。

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