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Kinetics and products of the degradation of chitosan by hydrogen peroxide

机译:过氧化氢降解壳聚糖的动力学及产物

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Low concentrations of hydrogen peroxide induced random degradation of partially deacetylated chitin and chitosan. Average molecular weight decreased in accordance with first-order kinetics. The degradation rate was much faster than that of the ultrasonic degradation, and it was comparable to that of the enzymatic hydrolysis of chitosan. Chain-end scissions occurred after chitosan was degraded severely and produced significant amounts of oligosaccharides at temperatures greater than or equal to 80 degreesC. Universal calibration moderated the change in molecular weight more closely than that calculated by the usual calibration using pullulan standards. Trace amounts of transition metal ions and the amino groups in. chitosan were critical to the breakdown of the beta -1,4 glycosidic linkages. HPLC results of glucosamine and chito-oligosaccharides could be characterized by, correlating the logarithmic values of retention time with the degrees of polymerization. The formation of glucosamine and chito-oligosaccharides depended on the concentration of H2O2, temperature, and the physicochemical property of chitin/chitosan.
机译:低浓度的过氧化氢可引起部分脱乙酰化的几丁质和壳聚糖的随机降解。平均分子量根据一级动力学而降低。降解速率比超声降解的速率快得多,并且与壳聚糖的酶水解相当。壳聚糖严重降解并在大于或等于80摄氏度的温度下产生大量的寡糖后,发生链末端断裂。通用校准比使用普鲁兰聚糖标准品进行的常规校准所计算的分子量更能缓和分子量的变化。壳聚糖中的痕量过渡金属离子和氨基对β-1,4糖苷键的破坏至关重要。可以通过将保留时间的对数值与聚合度相关联来表征氨基葡萄糖和壳寡糖的HPLC结果。氨基葡萄糖和壳寡糖的形成取决于过氧化氢的浓度,温度和几丁质/壳聚糖的理化性质。

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