植物生物质组分水解是天然和合成材料生态安全的普遍机制

A. Ivankin, A. Zarubinа, A. Verevkin, M. Baburina
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摘要

植物材料的蛋白质-多糖组分在基本环境条件下的水解是自然界生物质生化降解的主要机制。大多数现代合成高分子材料在其使用寿命结束后不具备在环境中迅速降解的能力。本研究的目的是比较植物来源的蛋白质多糖物质和人工合成的具有生物标记单位的聚合物材料的水解动力学。本文以大豆来源的植物蛋白和植物碳水化合物淀粉为例,研究了天然材料基本组分的水解动力学,并与用于木制品表面处理的合成共聚物甘油-邻苯二酸酐共聚物的可能酶生物降解进行了比较。本文描述了一种通过在其结构中引入乳酸波动单元来修饰这种共聚物合成的可能方法,从而增加了聚合物材料的生物活性。揭示了合成三元共聚物组成中乳酸单元对其生物降解速率的影响。在模拟其在环境中可能的生物降解的条件下,确定了所研究对象的酶解衰变速率和活化能的主要动力学常数。合成的甘油、邻苯二酸酐和乳酸的三共聚物的最大胰腺生物降解速率常数Vmax.102的取值范围为0,24 mg/ml·min-1,而在1,43…2,29 mg /ml·min-1为蛋白-多糖底物。研究表明,蛋白质性质的物质具有最高的生物降解率,甘油与邻苯二甲酸酐合成的树脂形式的共聚物具有显著的生物降解抗性。通过在其结构中引入乳酸单元对这种共聚物进行改性,可以提高其生物可降解性。通过在合成聚合物的结构中引入乳酸单元来修饰其生态性能,从而提高其生物降解性的便利性已经得到证实。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Plant biomass components hydrolysis as universal mechanism for eco safety of natural and synthetic materials
Hydrolysis of protein-polysaccharide components of plant materials under basic environmental conditions is the main mechanism of biochemical degradation of biomass in nature. Most modern synthetic polymeric materials do not have the ability to rapidly degrade in the environment after the end of their useful life. The aim of the work was to compare the kinetics of hydrolysis of protein-polysaccharide substances of plant origin and artificially created synthetic polymeric materials with biomarker units. The article studies the kinetics of hydrolysis of the basic constituents of natural materials on the example of model systems — vegetable protein of soy origin and vegetable carbohydrate — starch in comparison with the possible enzymatic biodegradation of a synthetic copolymer used for surface treatment of wood products — a copolymer of glycerol and phthalic anhydride. A methodology for the possible modification of the synthesis of such copolymers by introducing lactic acid fluctuation units into their structure, which increase the bioactivity of the polymer material, is described. The effect of lactic acid units in the composition of synthetic tercopolymer on the rate of its biodegradation has been revealed. The main kinetic constants of the decay rates and activation energies of the enzymatic hydrolysis of the studied objects were determined under conditions simulating their possible biodegradation in the environment. The values of the constants of the maximum rates of pancreatic biodegradation Vmax.102, ranged from 0,24 mg/ml·min–1 for the synthesized tercopolymer of glycerol, phthalic anhydride and lactic acid compared with similar values at the level of 1,43...2,29 mg /ml·min–1 for protein-polysaccharide substrates. It is shown that substances of a protein nature have the highest rate of biodegradation, and a synthetic copolymer of glycerol and phthalic anhydride in the form of glyphthalic resin has a significant resistance to biodegradation. Modification of such a copolymer by introducing lactic acid units into its structure makes it possible to increase its biodegradability. The expediency of modifying the eco-properties of synthetic polymers by introducing lactic acid units into their structure, which increase the biodegradability, has been confirmed.
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