过硫酸根离子在硫酸水相中降解靛蓝胭脂红染料:动力学研究

IF 1.5 4区 化学 Q4 CHEMISTRY, PHYSICAL International Journal of Chemical Kinetics Pub Date : 2024-02-22 DOI:10.1002/kin.21710
Patricia Ese Umoru, Ikechukwu Ugbaga Nkole, Titus Tobechukwu Ezeh
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引用次数: 0

摘要

追求更清洁的环境是全球关注的问题。因此,我们对硫酸水溶液体系中过氧化二硫酸根离子降解靛蓝胭脂红染料(IC)的情况进行了研究,以期了解其降解动力学和机理。降解过程显示了[S2O82-]和[IC]的一阶动力学,IC 的降解摩尔比为 1:1:S2O82- 的降解摩尔比为 1:1。降解速率取决于体系离子强度和介质介电常数的变化。此外,添加的离子(NH4+ 和 NO3-)也会影响染料的降解速率,这进一步证实了离子强度变化的结果。排除了自由基参与的可能性。实验速率定律为(Kk3[H+])[IC][S2O82-]。由于降解过程中没有可检测到的中间产物,因此提出了一种外球机制。这项研究对于纺织业和医疗环境来说意义重大,因为它可以利用人们熟知的降解速率途径降低环境中的毒性。
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Degradation of indigo carmine dye with peroxydisulphate ion in aqueous sulphuric acid phase: Kinetic study

The quest for cleaner environments is a global concern. Hence, the investigation of degradation of the indigo carmine dye (IC) with peroxydisulphate ion in an aqueous sulphuric acid system with a view to understanding its kinetic degradation and mechanism. The degradation depicts first-order kinetics in [S2O82−] and [IC], and the degradation mole ratio of IC: S2O82− is 1:1. The degradation rate is dependent on the change in ionic strength and medium permittivity of the system. Also, added ions (NH4+ and NO3) influence the degradation rate of the dye which further supported the outcome of the change in ionic strength. Free radical participation is ruled out. The experimental rate law is given as (Kk3[H+])[IC][S2O82−]. Owing to the absence of detectable intermediates in the degradation process, an outer-sphere mechanism is proposed. The study is significant in textile industries and medical settings for making environments less toxic with a well-understood degradation rate pathway.

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来源期刊
CiteScore
3.30
自引率
6.70%
发文量
74
审稿时长
3 months
期刊介绍: As the leading archival journal devoted exclusively to chemical kinetics, the International Journal of Chemical Kinetics publishes original research in gas phase, condensed phase, and polymer reaction kinetics, as well as biochemical and surface kinetics. The Journal seeks to be the primary archive for careful experimental measurements of reaction kinetics, in both simple and complex systems. The Journal also presents new developments in applied theoretical kinetics and publishes large kinetic models, and the algorithms and estimates used in these models. These include methods for handling the large reaction networks important in biochemistry, catalysis, and free radical chemistry. In addition, the Journal explores such topics as the quantitative relationships between molecular structure and chemical reactivity, organic/inorganic chemistry and reaction mechanisms, and the reactive chemistry at interfaces.
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