KINETIC MODEL OF THIOUREA DIOXIDE DECOMPOSITION IN AQUEOUS SOLUTIONS OF DIFFERENT ACIDITY

IF 0.6 Q4 CHEMISTRY, MULTIDISCIPLINARY
Yu. V. Polenov, G. A. Shestakov, E. Egorova
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引用次数: 2

Abstract

A stoichiometric mechanism for full thiourea dioxide decomposition in aqueous solution under pH of 4.0 is proposed based on dependences of concentrations of thiourea dioxide and its decomposition products on the time and literature data. The concentration of thiourea dioxide was measured via iodometry, while the intermediates were quantified using the polarography. Polarography was carried out in glass two-electrode electrochemical cell by means of PU-1 polarograph in differential mode. Dropping mercury electrode was used as working one and silver chloride as a reference one. Rate constants for individual stages are obtained via mathematical modeling, presented a system of differential equations. Absolute errors of rate constants, correlation coefficients, and F-factors were also calculated. Verification of supposed kinetic model was conducted using the comparison between experimental and calculated concentrations, F-test and the calculated values of correlation coefficients of the individual stages of the process. Supposed kinetic model of decomposition consists of a number of consequent stages including various compounds such as sulfur monoxide, thiosulfuric, sulfuric, dithionic, hydrosulfuric acids as intermediates was used for previously obtained data for pH of 8.85. To test the universality of supposed model, we simulated kinetics of thiourea dioxide decomposition reaction at pH of 8.85. Experimental kinetic data were taken from literature. The initial approximations of the individual stages constants were taken from previous calculations. Analysis of calculated data: concentration values, F-test, correlation coefficients allowed to conclude about the applicability of proposed mechanism for the process of thiourea dioxide decomposition in a weakly alkaline medium.
不同酸度水溶液中二氧化硫脲分解动力学模型
基于二氧化硫及其分解产物浓度与时间和文献数据的关系,提出了pH为4.0的水溶液中二氧化硫完全分解的化学计量学机制。二氧化硫脲浓度采用碘量法测定,中间体采用极谱法测定。采用差模PU-1极谱仪对玻璃双电极电化学电池进行极谱分析。工作电极为滴汞电极,参比电极为氯化银电极。通过数学建模得到了各个阶段的速率常数,并给出了一个微分方程组。计算了速率常数、相关系数和f因子的绝对误差。通过实验浓度与计算浓度的比较、f检验和各阶段相关系数的计算值,对假设的动力学模型进行了验证。假设的分解动力学模型包括许多后续阶段,包括各种化合物,如一氧化碳,硫代硫酸,硫代硫酸,二硫代酸,氢硫酸作为中间体,用于先前获得的pH为8.85的数据。为了验证所假设模型的普遍性,我们模拟了pH为8.85时二氧化硫脲分解反应的动力学。实验动力学数据来源于文献。各个阶段常数的初始近似值是从以前的计算中得到的。计算数据的分析:浓度值、f检验、相关系数,从而得出所提出的机制在弱碱性介质中二氧化硫脲分解过程的适用性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.40
自引率
44.40%
发文量
83
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