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Kinetics of colloidal MnO_2 reduction by L-arginine in absence and presence of surfactants

机译:在表面活性剂不存在下L-精氨酸还原胶体MnO_2的动力学

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The kinetics of the oxidation of L-arginine by water-soluble form of colloidal manganese dioxide has been studied using visible spectrophotometry in aqueous as well as micellar media. To obtain the rate constants as functions of [L-arginine], [MnO_2] and [HClO_4], pseudo-first-order conditions are maintained in each kinetic run. The first-order-rate is observed with respect to [MnO_2], whereas fractional-order-rates are determined in both [L-arginine] and [HClO_4]. Addition of sodium pyrophosphate and sodium fluoride enhanced the rate of the reaction. The effect of externally added manganese(II) sulphate is complex. It is not possible to predict the exact dependence of the rate constant on manganese(II) concentration, which has a series of reactions with other reactants. The anionic surfactant SDS neither catalyzed nor inhibited the oxidation reaction, while in presence of cationic surfactant CTAB the reaction is not possible due to flocculation of reaction mixture. The reaction is catalyzed by the nonionic surfactant TX-100 which is explained in terms of the mathematical model proposed by Tuncay et al. Activation parameters have been evaluated using Arrhenius and Eyring equations. On the basis of observed kinetic results, a probable mechanism for the reaction has been proposed which corresponds to fast adsorption of the reductant and hydrogen ion on the urface of colloidal MnO_2.
机译:使用可见分光光度法在水性和胶束介质中研究了水溶性水溶性胶态二氧化锰对L-精氨酸的氧化动力学。为了获得作为[L-精氨酸],[MnO_2]和[HClO_4]的函数的速率常数,在每个动力学过程中都保持伪一阶条件。观察到相对于[MnO_2]的一阶速率,而在[L-精氨酸]和[HClO_4]中都确定了分数阶速率。焦磷酸钠和氟化钠的加入提高了反应速率。外部添加硫酸锰(II)的效果很复杂。无法预测速率常数对锰(II)浓度的确切依赖性,锰与其他反应物会发生一系列反应。阴离子表面活性剂SDS既不催化也不抑制氧化反应,而在阳离子表面活性剂CTAB的存在下,由于反应混合物的絮凝,该反应是不可能的。该反应由非离子表面活性剂TX-100催化,该表面活性剂根据Tuncay等人提出的数学模型进行解释。激活参数已使用Arrhenius和Eyring方程进行了评估。基于观察到的动力学结果,已经提出了反应的可能机理,其对应于还原剂和氢离子在胶体MnO_2表面上的快速吸附。

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