{"title":"Enhancing the degradation of 2,4-dinitrotoluene using zero-valent magnesium in the presence of persulfate and hydrogen peroxide","authors":"Seok-Young Oh, Kideok Kim","doi":"10.1016/j.jwpe.2025.107485","DOIUrl":null,"url":null,"abstract":"<div><div>The degradation of 2,4-dinitrotoluene (DNT) by persulfate and hydrogen peroxide in the presence of zero-valent magnesium (Mg(0)) was examined in a series of batch experiments. The degradation of DNT by Mg(0) alone was limited to 32 % after 24 h due to the rapid oxidation of Mg(0) and the formation of a passivation layer in the presence of oxygen. However, the combination of Mg(0) with persulfate or hydrogen peroxide greatly enhanced the degradation of DNT to 65 % and 90 % after 24 h, respectively. Quenching experiments with radical scavengers and electron paramagnetic resonance spectroscopy analysis showed that sulfate (SO<sub>4</sub><sup>−</sup>·) and hydroxyl (OH·) radicals were responsible for the enhancement of DNT degradation in the Mg(0)-persulfate/hydrogen peroxide systems. Analyses of total organic carbon and 5-day biochemical oxygen demand revealed that non-mineralized by-products remained in the systems and that the biodegradability of the non-mineralized by-products was significantly enhanced. To further enhance the degradation of DNT using the Mg(0)–persulfate/hydrogen peroxide systems, stepwise dosing of Mg(0) was employed, leading to DNT degradation rates of 83 % and 77 % after 2.5 h with persulfate and hydrogen peroxide, respectively. Co-catalysis of Mg(0) with Fe(0) also significantly improved the DNT degradation in the persulfate/hydrogen peroxide systems, with the complete degradation of DNT after 4 h. The sonication of Mg(0) also led to the complete degradation of DNT after 2 and 3 h with persulfate and hydrogen peroxide, respectively. Our results suggest that Mg(0) is a promising reductant and an effective catalyst for the degradation of DNT in persulfate/hydrogen peroxide systems.</div></div>","PeriodicalId":17528,"journal":{"name":"Journal of water process engineering","volume":"73 ","pages":"Article 107485"},"PeriodicalIF":6.3000,"publicationDate":"2025-03-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of water process engineering","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2214714425005574","RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, CHEMICAL","Score":null,"Total":0}
引用次数: 0
Abstract
The degradation of 2,4-dinitrotoluene (DNT) by persulfate and hydrogen peroxide in the presence of zero-valent magnesium (Mg(0)) was examined in a series of batch experiments. The degradation of DNT by Mg(0) alone was limited to 32 % after 24 h due to the rapid oxidation of Mg(0) and the formation of a passivation layer in the presence of oxygen. However, the combination of Mg(0) with persulfate or hydrogen peroxide greatly enhanced the degradation of DNT to 65 % and 90 % after 24 h, respectively. Quenching experiments with radical scavengers and electron paramagnetic resonance spectroscopy analysis showed that sulfate (SO4−·) and hydroxyl (OH·) radicals were responsible for the enhancement of DNT degradation in the Mg(0)-persulfate/hydrogen peroxide systems. Analyses of total organic carbon and 5-day biochemical oxygen demand revealed that non-mineralized by-products remained in the systems and that the biodegradability of the non-mineralized by-products was significantly enhanced. To further enhance the degradation of DNT using the Mg(0)–persulfate/hydrogen peroxide systems, stepwise dosing of Mg(0) was employed, leading to DNT degradation rates of 83 % and 77 % after 2.5 h with persulfate and hydrogen peroxide, respectively. Co-catalysis of Mg(0) with Fe(0) also significantly improved the DNT degradation in the persulfate/hydrogen peroxide systems, with the complete degradation of DNT after 4 h. The sonication of Mg(0) also led to the complete degradation of DNT after 2 and 3 h with persulfate and hydrogen peroxide, respectively. Our results suggest that Mg(0) is a promising reductant and an effective catalyst for the degradation of DNT in persulfate/hydrogen peroxide systems.
期刊介绍:
The Journal of Water Process Engineering aims to publish refereed, high-quality research papers with significant novelty and impact in all areas of the engineering of water and wastewater processing . Papers on advanced and novel treatment processes and technologies are particularly welcome. The Journal considers papers in areas such as nanotechnology and biotechnology applications in water, novel oxidation and separation processes, membrane processes (except those for desalination) , catalytic processes for the removal of water contaminants, sustainable processes, water reuse and recycling, water use and wastewater minimization, integrated/hybrid technology, process modeling of water treatment and novel treatment processes. Submissions on the subject of adsorbents, including standard measurements of adsorption kinetics and equilibrium will only be considered if there is a genuine case for novelty and contribution, for example highly novel, sustainable adsorbents and their use: papers on activated carbon-type materials derived from natural matter, or surfactant-modified clays and related minerals, would not fulfil this criterion. The Journal particularly welcomes contributions involving environmentally, economically and socially sustainable technology for water treatment, including those which are energy-efficient, with minimal or no chemical consumption, and capable of water recycling and reuse that minimizes the direct disposal of wastewater to the aquatic environment. Papers that describe novel ideas for solving issues related to water quality and availability are also welcome, as are those that show the transfer of techniques from other disciplines. The Journal will consider papers dealing with processes for various water matrices including drinking water (except desalination), domestic, urban and industrial wastewaters, in addition to their residues. It is expected that the journal will be of particular relevance to chemical and process engineers working in the field. The Journal welcomes Full Text papers, Short Communications, State-of-the-Art Reviews and Letters to Editors and Case Studies