{"title":"Self-enhanced oxidation of resistant monocyclic aromatic compounds during ozone treatment: Applicability in groundwater remediation","authors":"Anwar Dawas , Emil Bein , Yinon Yecheskel , Tamir Ouddiz , Uwe Hübner , Ines Zucker","doi":"10.1016/j.gsd.2024.101222","DOIUrl":null,"url":null,"abstract":"<div><p>The Peroxone process—which utilizes a combination of ozone and hydrogen peroxide to generate hydroxyl radicals—is frequently used in groundwater remediation to effectively remove ozone-resistant contaminants. However, some monocyclic aromatic compounds with low ozone reactivity have been found to be removed by ozone solely (without the need for hydrogen peroxide) through a self-enhanced mechanism. This self-enhanced removal occurs when the interaction of ozone with hydroxide ion generates sufficient amount of hydroxyl radicals, initiating a radical reaction that subsequently propagates through the degradation intermediates. This study leverages the self-enhanced degradation mechanism for the treatment of ozone-resistant compounds during groundwater remediation. Key environmental conditions, including water alkalinity and contaminant concentration, were investigated for their effect on the self-enhanced degradation of <em>para</em>-chloro benzoic acid (pCBA), which served as a model for ozone-resistant compounds. High pCBA removal was observed during ozonation in the concentration range of 0.5–5 μM, where the decay kinetics of pCBA and ozone significantly dependent on the initial pCBA concentration. Furthermore, decreased pCBA removal was noted in water matrices with increased alkalinity, largely due to the scavenging of OH radicals by carbonate species. Finally, pCBA removal was investigated in natural groundwater, where co-existing substances acted as ozone/radical scavengers, leading to reduced pCBA removal. Overall, this study highlights the importance of the self-enhanced removal mechanism of monocyclic aromatic contaminants when treating water with high contamination levels and low-to-moderate alkalinities.</p></div>","PeriodicalId":37879,"journal":{"name":"Groundwater for Sustainable Development","volume":null,"pages":null},"PeriodicalIF":4.9000,"publicationDate":"2024-06-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Groundwater for Sustainable Development","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2352801X24001450","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENGINEERING, ENVIRONMENTAL","Score":null,"Total":0}
引用次数: 0
Abstract
The Peroxone process—which utilizes a combination of ozone and hydrogen peroxide to generate hydroxyl radicals—is frequently used in groundwater remediation to effectively remove ozone-resistant contaminants. However, some monocyclic aromatic compounds with low ozone reactivity have been found to be removed by ozone solely (without the need for hydrogen peroxide) through a self-enhanced mechanism. This self-enhanced removal occurs when the interaction of ozone with hydroxide ion generates sufficient amount of hydroxyl radicals, initiating a radical reaction that subsequently propagates through the degradation intermediates. This study leverages the self-enhanced degradation mechanism for the treatment of ozone-resistant compounds during groundwater remediation. Key environmental conditions, including water alkalinity and contaminant concentration, were investigated for their effect on the self-enhanced degradation of para-chloro benzoic acid (pCBA), which served as a model for ozone-resistant compounds. High pCBA removal was observed during ozonation in the concentration range of 0.5–5 μM, where the decay kinetics of pCBA and ozone significantly dependent on the initial pCBA concentration. Furthermore, decreased pCBA removal was noted in water matrices with increased alkalinity, largely due to the scavenging of OH radicals by carbonate species. Finally, pCBA removal was investigated in natural groundwater, where co-existing substances acted as ozone/radical scavengers, leading to reduced pCBA removal. Overall, this study highlights the importance of the self-enhanced removal mechanism of monocyclic aromatic contaminants when treating water with high contamination levels and low-to-moderate alkalinities.
期刊介绍:
Groundwater for Sustainable Development is directed to different stakeholders and professionals, including government and non-governmental organizations, international funding agencies, universities, public water institutions, public health and other public/private sector professionals, and other relevant institutions. It is aimed at professionals, academics and students in the fields of disciplines such as: groundwater and its connection to surface hydrology and environment, soil sciences, engineering, ecology, microbiology, atmospheric sciences, analytical chemistry, hydro-engineering, water technology, environmental ethics, economics, public health, policy, as well as social sciences, legal disciplines, or any other area connected with water issues. The objectives of this journal are to facilitate: • The improvement of effective and sustainable management of water resources across the globe. • The improvement of human access to groundwater resources in adequate quantity and good quality. • The meeting of the increasing demand for drinking and irrigation water needed for food security to contribute to a social and economically sound human development. • The creation of a global inter- and multidisciplinary platform and forum to improve our understanding of groundwater resources and to advocate their effective and sustainable management and protection against contamination. • Interdisciplinary information exchange and to stimulate scientific research in the fields of groundwater related sciences and social and health sciences required to achieve the United Nations Millennium Development Goals for sustainable development.