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Biodegradation and Characterization Studies of Different Kinds of Polyurethanes with Several Enzyme Solutions

机译:几种酶溶液对不同类型聚氨酯的生物降解与表征研究

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In the present work, biodegradation behaviors compared commercial polyurethane to synthesized polyurethane in different enzyme solutions. Two quantitative methods have been used to follow the biodegradation. Enzymes were esterase and protease in the hydrolase class; enzyme solutions were prepared one by one or by combining as enzyme cocktail solutions. Esterase affect ester bonds whereas protease enzymes affect urethane and urea linkages. Thus, effects of enzyme cocktail solutions were also researched in this study. It is a new way for in vitro degradation of polyurethane samples by enzyme cocktail solutions, lcmx lcm of polyurethane films were put in a tube and treated by different combinations of these mentioned enzymes. The tubes were placed in a shaker and stirred at 120 rpm under the reaction condition of 37°C and pH 7.4. In order to keep enzymatic activity stable, enzyme solutions were prepared again periodically. All samples were characterized by Fourier transform infrared spectroscopy and scanning electron microscopy. The bond strength of chains and morphological changes were recorded during the period of biodegradation. The results showed that protease enzyme solutions could erode polymer films, but esterase enzyme solution could not be so effective alone. In addition, enzyme cocktail solutions showed that enzymes could compete with each other, so one enzyme could suppress the activity of another enzyme.
机译:在目前的工作中,生物降解行为在不同的酶溶液中将商品聚氨酯与合成聚氨酯进行了比较。已经使用两种定量方法来追踪生物降解。酶是水解酶类别的酯酶和蛋白酶;酶溶液一一制备或作为酶混合物溶液制备。酯酶影响酯键,而蛋白酶则影响氨基甲酸酯和脲键。因此,在该研究中还研究了酶混合物溶液的作用。这是一种通过酶混合物溶液体外降解聚氨酯样品的新方法,将1cmx 1cm的聚氨酯薄膜放入试管中,并通过上述酶的不同组合进行处理。将试管置于振荡器中,并在37℃和pH 7.4的反应条件下以120rpm搅拌。为了保持酶活性稳定,再次定期制备酶溶液。所有样品均通过傅里叶变换红外光谱和扫描电子显微镜进行表征。在生物降解期间记录了链的键强度和形态变化。结果表明,蛋白酶溶液可以腐蚀聚合物薄膜,但是酯酶溶液不能单独如此有效。此外,酶混合物溶液显示酶可以相互竞争,因此一种酶可以抑制另一种酶的活性。

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