Micellar Effects on the Chromium(VI) Oxidation of d (+)-Xylose

Kabir-ud-din, A. Morshed, Z. Khan
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引用次数: 11

Abstract

Chromic acid oxidation of d (+)-xylose in water and in presence of surfactants has an induction period followed by autoacceleration. The kinetics and mechanism of the induction period have been studied spectrophotometrically in both media. Due to precipitate formation, the effect of cetyltrimethylammonium bromide (CTAB, cationic) cannot be studied whereas the oxidation rate increased with increase in sodium dodecyl sulphate (SDS, an-ionic) and octylphenoxypolyethoxy ethanol (TX-100, nonionic) concentration. Reaction is routed through the same mechanism as shown by the kinetic study in the absence and presence of surfactants. Micellar catalysis has been traced to partitioning of the chromic acid species and xylose between the aqueous and micellar pseudo-phases. Rate enhancement in SDS micelles is decreased by ammonium, lithium and sodium ions. Micellar binding/association constants and activation parameters were evaluated and discussed. A mechanism consistent with the results is proposed.
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胶束对d(+)-木糖铬(VI)氧化的影响
铬酸氧化d(+)-木糖在水中和表面活性剂存在下有一个诱导期,随后有一个自加速期。用分光光度法研究了两种介质中诱导期的动力学和机理。由于沉淀的形成,十六烷基三甲基溴化铵(CTAB,阳离子)的影响无法研究,而氧化速率随着十二烷基硫酸钠(SDS,非离子)和辛基苯氧聚氧基乙醇(TX-100,非离子)浓度的增加而增加。在没有和存在表面活性剂的情况下,反应的机理与动力学研究显示的相同。胶束催化可以追溯到铬酸和木糖在水相和胶束伪相之间的分配。铵离子、锂离子和钠离子降低了SDS胶束的速率增强。对胶束结合/结合常数和活化参数进行了评价和讨论。提出了一种与结果一致的机理。
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