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Kinetics and mechanism of permanganate oxidation of iota- and lambda-carrageenan polysaccharides as sulfated carbohydrates in acid perchlorate solutions

机译:高碘酸盐溶液中高碘酸盐氧化硫酸化碳水化合物的高碘酸盐和碘化角叉菜胶多糖的动力学和机理

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摘要

The kinetics of oxidation of iota- and lambda-carrageenan as sulfated carbohydrates by permanganate ion in aqueous perchlorate solutions at a constant ionic strength of 2.0 mol dm~(-3) have been investigated spectrophotometrically. The pseudo-first-order plots were found to be of inverted S-shape throughout the entire courses of reactions. The initial rates were found to be relatively slow in the early stages, followed by an increase in the oxidation rates over longer time periods. The experimental observations showed first-order dependences in permanganate and fractional first-order kinetics with respect to both carrageenans concentration for both the induction and autoacceleration periods. The results obtained at various hydrogen ion concentrations showed that the oxidation processes in these redox systems are acid-catalyzed throughout the two stages of oxidation reactions. The added salts lead to the prediction that Mn~(III) is the reactive species throughout the autoacceleration periods. Kinetic evidence for the formation of 1:1 intermediate complexes was revealed. The kinetic parameters have been evaluated and tentative reaction mechanisms in good agreement with the kinetic results are discussed.
机译:研究了高氯酸盐水溶液中高锰酸根离子在2.0 mol dm〜(-3)的恒定离子强度下,氧化碘代-角叉菜胶和λ-角叉菜胶作为硫酸化碳水化合物的动力学。发现伪一阶图在整个反应过程中呈倒S形。发现在初期,初始速率相对较慢,随后在较长时间内氧化速率增加。实验观察结果表明,在诱导期和自加速期,高锰酸盐和分数一级动力学相对于角叉菜胶浓度均呈一阶依赖性。在各种氢离子浓度下获得的结果表明,在整个氧化反应的两个阶段中,这些氧化还原系统中的氧化过程均被酸催化。所添加的盐导致在整个自动加速期间Mn〜(III)是反应性物质的预测。揭示了形成1:1中间体配合物的动力学证据。动力学参数已进行了评估,初步的反应机理与动力学结果进行了讨论。

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