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      Insights into the role of nanoscale zero‐valent iron in Fenton oxidation and its application in naphthalene degradation from water and slurry systems

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          Abstract

          Few researches have focused on the role of nanoscale zero‐valent iron (nZVI) in Fenton‐like process for polycyclic aromatic hydrocarbons (PAHs) removal. In this study, the naphthalene (NAP) degradation tests in ultrapure water showed that nZVI addition could enhance NAP degradation from 79.7% to 99.0% in hydrogen peroxide (H 2O 2)/Fe (II)/nZVI/NAP system at the molar ratio of 10/5/3/1, showing the excellent role of nZVI in promoting NAP removal. Multiple linear regression analysis found that the correlation coefficient between H 2O 2 consumption and NAP degradation was converted from −9.17 to 0.48 with nZVI and 1‐mM H 2O 2, indicating that nZVI could decompose H 2O 2 more beneficially for NAP degradation. Multiple Fe (II)‐dosing and iron leaching tests revealed that nZVI could gently liberate Fe (II) and promote Fe (II)/Fe (III) redox cycle to enhance the NAP degradation. When the H 2O 2/Fe (II)/nZVI/NAP molar ratios of 10/5/3/1 and 50/25/15/1 were applied in the simulated NAP contaminated actual groundwater and soil slurry, respectively, 75.0% and 82.9% of NAP removals were achieved. Based on the major degradation intermediates detected by GC/MS, such as 1,4‐naphthalenedione, cinnamaldehyde, and o‐phthalaldehyde, three possible NAP degradation pathways were proposed. This study provided the applicable potential of nZVI in Fenton process for PAHs contaminated groundwater and soil remediation.

          Practitioner Points

          • nZVI enhanced the NAP degradation in Fenton‐like process.

          • Three schemes of NAP degradation pathway were proposed.

          • nZVI performed well in the remediation of the simulated NAP contamination.

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          Most cited references46

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          Reactive species in advanced oxidation processes: Formation, identification and reaction mechanism

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            Production of sulfate radical and hydroxyl radical by reaction of ozone with peroxymonosulfate: a novel advanced oxidation process.

            In this work, simultaneous generation of hydroxyl radical (•OH) and sulfate radical (SO4•−) by the reaction of ozone (O3) with peroxymonosulfate (PMS; HSO5−) has been proposed and experimentally verified. We demonstrate that the reaction between the anion of PMS (i.e.,SO52−) and O3 is primarily responsible for driving O3 consumption with a measured second order rate constant of (2.12 ± 0.03) × 10(4) M(-1) s(-1). The formation of both •OH and SO4•− from the reaction between SO52− and O3 is confirmed by chemical probes (i.e., nitrobenzene for •OH and atrazine forb oth •OH and SO4•−). The yields of •OH and SO4•− are determined to be 0.43 ± 0.1 and 0.45 ± 0.1 per mol of O3 consumption, respectively. An adduct,−O3SOO− + O3 → −O3SO5−, is assumed as the first step, which further decomposes into SO5•− and O3•−. The subsequent reaction of SO5•− with O3is proposed to generate SO4•−, while O3•− converts to •OH. A definition of R(ct,•OH) and R(ct,SO4•−) (i.e., respective ratios of •OH and SO4•− exposures to O3 exposure) is adopted to quantify relative contributions of •OH and SO4•−. Increasing pH leads to increases in both values of R(ct,•OH) and R(ct,SO4•−) but does not significantly affect the ratio of R(ct,SO4•−) to R(ct,•OH) (i.e., R(ct,SO4•−)/R(ct,•OH)), which represents the relative formation of SO4•− to •OH. The presence of bicarbonate appreciably inhibits the degradation of probes and fairly decreases the relative contribution of •OH for their degradation, which may be attributed to the conversion of both •OH and SO4•− to the more selective carbonate radical (CO3•−).Humic acid promotes O3 consumption to generate •OH and thus leads to an increase in the R(ct,•OH) value in the O3/PMS process,w hile humic acid has negligible influence on the R(ct,SO4•−) value. This discrepancy is reasonably explained by the negligible effect of humic acid on SO4•− formation and a lower rate constant for the reaction of humic acid with SO4•− than with •OH. In addition, the efficacy of the O3/PMS process in real water is also confirmed.
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              Hydroxyl radical generation by zero-valent iron/Cu (ZVI/Cu) bimetallic catalyst in wastewater treatment: Heterogeneous Fenton/Fenton-like reactions by Fenton reagents formed in-situ under oxic conditions

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                Author and article information

                Contributors
                Journal
                Water Environment Research
                Water Environment Research
                Wiley
                1061-4303
                1554-7531
                April 2022
                April 03 2022
                April 2022
                : 94
                : 4
                Affiliations
                [1 ] State Environmental Protection Key Laboratory of Environmental Risk Assessment and Control on Chemical Process East China University of Science and Technology Shanghai China
                [2 ] Department of Chemical Engineering MNS University of Engineering and Technology Multan Pakistan
                Article
                10.1002/wer.10710
                530467b3-8bb3-427d-82c0-9621dcd47fbf
                © 2022

                http://onlinelibrary.wiley.com/termsAndConditions#vor

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