二甲亚砜水溶液氧化过程的动力学研究

Saif Ali Abdulhadi, Alona Tulskа, Volodymyr Bayrachnyi, I. Sinkevich
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引用次数: 0

摘要

二甲基亚砜是合成大量有机物的原料。目前研究的重点是二甲亚砜氧化的一般产品-二甲砜和甲烷磺酸的生产。二甲基砜是一种众所周知的食物补充剂,用于治疗和加强人体关节和韧带。二甲基砜的基本合成方法是将二甲基亚砜在30%过氧化氢的冰乙酸中氧化。合成过程中伴随着过氧化氢的大量损失,目标产物必须经过大量纯化。采用耐化学阳极和高氧过电压氧化二甲基亚砜水溶液的电化学方法,使控制纯二甲砜和甲烷磺酸的合成成为可能,因为硫容易改变氧化速率。在二甲基亚砜浓度1.0 ~ 4.0 mol∙dm-3范围内,研究了铂电极上阳极氧化过程的动力学。当电位大于1.3…1.4 V时,观察到电流升高。这个电位范围对应于氧释放。加入溶解硫酸(0.2 mol∙dm-3)抑制氧释放,达到过氧化自由基在二甲亚砜水溶液中形成的潜力。已知硫酸根离子被吸附在铂阳极表面,取代质子化水分子。这允许在0.2 mol∙dm-3 H2SO4中移动电位并将电解电流增加到1.7…1.9 V。它表明了在铂阳极表面过氧化自由基的形成过程。阳极电位进一步移动到比2.00 ~ 2.05 V更正的区域,导致电流密度迅速增加。在这样的电位下,二甲亚砜和二甲砜通过平行的氧和过氧化氢释放被氧化成甲烷磺酸。电流-电压研究表明,水溶液中二甲亚砜的氧化是通过二甲砜的形成来进行的。在控制阳极电位的情况下进行电化学合成时,可以在不进一步氧化为甲烷磺酸的情况下生产二甲基砜。在二甲亚砜水溶液中加入0.2 mol∙dm-3 H2SO4可抑制氧的释放,并增强吸附在铂表面的偶极子二甲亚砜分子的氧化。研究了高阳极电位下铂阳极在二甲亚砜水溶液中吸附过程对阳极过程动力学的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
ON THE KINETICS OF ANODIC PROCESSES AT OXIDATION OF AQUEOUS SOLUTIONS OF DIMETHYL SULFOXIDE
Dimethyl sulfoxide is a feedstock for a large number of organic substances syntheses. Nowadays research is considerably focused on the production of general products of dimethyl sulfoxide oxidation – dimethyl sulfone and methane sulfonic acid. Dimethyl sulfone is well–known as a food supplement for the treating and strengthening of human joints and ligaments. dimethyl sulfone is basically synthesized by oxidation of dimethyl sulfoxide in hot 30 % hydrogen peroxide in glacial acetic acid. Synthesis is accompanied by significant losses of hydrogen peroxide, the target product has to be significantly purified. It becomes possible to control the synthesis of pure dimethyl sulfone and methane sulfonic acid when using the electrochemical method of oxidation of dimethyl sulfoxide in its aqueous solution with chemically resistant anode and high overvoltage of oxygen reaction Controlled synthesis is relevant because sulfur tends to change the oxidation rate. Study of kinetics of anodic processes at platinum electrode was performed in the dimethyl sulfoxide concentration range about 1.0…4.0 mol∙dm–3. Current raise was observed at potentials that are more positive than 1.3…1.4 V. This potential range corresponds to oxygen release. Dissolved sulfuric acid (0.2 mol∙dm–3) was added in order to inhibit the oxygen release and achieve the potential for the formation of peroxide radicals in aqueous solutions of dimethyl sulfoxide. It is known that sulfate ions are adsorbed on the surface of the platinum anode, displacing molecules of protonated water. This allows to shift the potentials and increase of the electrolysis current in 0.2 mol∙dm–3 H2SO4 to 1.7…1.9 V. It indicates the processes of formation of peroxide radicals on the surface of the platinum anode. Further shift of the anode potential into more positive area than 2.00…2.05 V leads to a rapid increase in current density. At such potentials, dimethyl sulfoxide and dimethyl sulfone are oxidized to methane sulfonic acid with a parallel oxygen and hydrogen peroxide release. Current–voltage study has shown that the oxidation of dimethyl sulfoxide in aqueous solutions runs through the formation of dimethyl sulfone. When conducting electrochemical synthesis with control of the anode potential, it is possible to produce dimethyl sulfone without further oxidation to methane sulfonic acid. The addition of 0.2 mol∙dm–3 H2SO4 to aqueous dimethyl sulfoxide solutions inhibits oxygen release and intensifies oxidation of dipole dimethyl sulfoxide molecules adsorbed on the platinum surface. The influence of adsorption processes on the kinetics of anode processes at the platinum anode in aqueous solutions of dimethyl sulfoxide at high anode potentials has been studied.
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