Catalytic Ozonation of Nitrobenzene by Manganese-Based Y Zeolites

Catalytic ozonation process (COP) is considered as a cost-efficient technology for the treatment of refractory chemical wastewaters. The catalyst performance plays an important role for the treatment efficiency. The present study investigated efficiencies and mechanisms of manganese (Mn)-based Y zeo...

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Main Authors: Jingze Hu, Yiming Li, Shaoshuai Nan, Brandon A. Yoza, Yifan Li, Yali Zhan, Qinghong Wang, Qing X. Li, Shaohui Guo, Chunmao Chen
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-02-01
Series:Frontiers in Chemistry
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fchem.2020.00080/full
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spelling doaj-3d309791aa7549a4a9a60d0867b60f152020-11-25T02:56:54ZengFrontiers Media S.A.Frontiers in Chemistry2296-26462020-02-01810.3389/fchem.2020.00080504678Catalytic Ozonation of Nitrobenzene by Manganese-Based Y ZeolitesJingze Hu0Yiming Li1Shaoshuai Nan2Brandon A. Yoza3Yifan Li4Yali Zhan5Qinghong Wang6Qing X. Li7Shaohui Guo8Chunmao Chen9State Key Laboratory of Petroleum Pollution Control, China University of Petroleum-Beijing, Beijing, ChinaState Key Laboratory of Petroleum Pollution Control, China University of Petroleum-Beijing, Beijing, ChinaState Key Laboratory of Petroleum Pollution Control, China University of Petroleum-Beijing, Beijing, ChinaHawaii Natural Energy Institute, University of Hawaii at Manoa, Honolulu, HI, United StatesState Key Laboratory of Petroleum Pollution Control, China University of Petroleum-Beijing, Beijing, ChinaState Key Laboratory of Petroleum Pollution Control, China University of Petroleum-Beijing, Beijing, ChinaState Key Laboratory of Petroleum Pollution Control, China University of Petroleum-Beijing, Beijing, ChinaDepartment of Molecular Biosciences and Bioengineering, University of Hawaii at Manoa, Honolulu, HI, United StatesState Key Laboratory of Petroleum Pollution Control, China University of Petroleum-Beijing, Beijing, ChinaState Key Laboratory of Petroleum Pollution Control, China University of Petroleum-Beijing, Beijing, ChinaCatalytic ozonation process (COP) is considered as a cost-efficient technology for the treatment of refractory chemical wastewaters. The catalyst performance plays an important role for the treatment efficiency. The present study investigated efficiencies and mechanisms of manganese (Mn)-based Y zeolites in COPs for removing nitrobenzene from water. The catalysts of Mn/NaY and Mn/USY were prepared by incipient wetness impregnation, while Mn-USY was obtained by hydrothermal synthesis. Mn-USY contained a greater ratio of Mn2+ than Mn/NaY, and Mn/USY. Mn oxides loaded on Y zeolites promoted the COP efficiencies. Mn/NaY increased total organic carbon removal in COP by 7.3% compared to NaY, while Mn/USY and Mn-USY increased 11.5 and 15.8%, respectively, relative to USY in COP. Multivalent Mn oxides (Mn2+, Mn3+, and Mn4+) were highly dispersed on the surface of NaY or USY, and function as catalytic active sites, increasing mineralization. Mn-USY showed the highest total organic carbon removal (44.3%) in COP among the three catalysts, because Mn-USY had a higher ratio of Mn2+ to the total Mn oxides on the surface than Mn/NaY and Mn/USY and the catalytic effects from intercorrelations between Mn oxides and mesoporous surface structures. The hydroxyl radicals and superoxide radicals governed oxidations in COP using Mn-USY. Nitrobenzene was oxidized to polyhydroxy phenol, polyhydroxy nitrophenol, and p-benzoquinone. The intermediates were then oxidized to small organic acids and ultimately carbon dioxide and water. This study demonstrates the potential of Y zeolites used in COP for the treatment of refractory chemical wastewaters.https://www.frontiersin.org/article/10.3389/fchem.2020.00080/fullozonationcatalytic ozonationY zeolitesMn oxideswastewater treatment
collection DOAJ
language English
format Article
sources DOAJ
author Jingze Hu
Yiming Li
Shaoshuai Nan
Brandon A. Yoza
Yifan Li
Yali Zhan
Qinghong Wang
Qing X. Li
Shaohui Guo
Chunmao Chen
spellingShingle Jingze Hu
Yiming Li
Shaoshuai Nan
Brandon A. Yoza
Yifan Li
Yali Zhan
Qinghong Wang
Qing X. Li
Shaohui Guo
Chunmao Chen
Catalytic Ozonation of Nitrobenzene by Manganese-Based Y Zeolites
Frontiers in Chemistry
ozonation
catalytic ozonation
Y zeolites
Mn oxides
wastewater treatment
author_facet Jingze Hu
Yiming Li
Shaoshuai Nan
Brandon A. Yoza
Yifan Li
Yali Zhan
Qinghong Wang
Qing X. Li
Shaohui Guo
Chunmao Chen
author_sort Jingze Hu
title Catalytic Ozonation of Nitrobenzene by Manganese-Based Y Zeolites
title_short Catalytic Ozonation of Nitrobenzene by Manganese-Based Y Zeolites
title_full Catalytic Ozonation of Nitrobenzene by Manganese-Based Y Zeolites
title_fullStr Catalytic Ozonation of Nitrobenzene by Manganese-Based Y Zeolites
title_full_unstemmed Catalytic Ozonation of Nitrobenzene by Manganese-Based Y Zeolites
title_sort catalytic ozonation of nitrobenzene by manganese-based y zeolites
publisher Frontiers Media S.A.
series Frontiers in Chemistry
issn 2296-2646
publishDate 2020-02-01
description Catalytic ozonation process (COP) is considered as a cost-efficient technology for the treatment of refractory chemical wastewaters. The catalyst performance plays an important role for the treatment efficiency. The present study investigated efficiencies and mechanisms of manganese (Mn)-based Y zeolites in COPs for removing nitrobenzene from water. The catalysts of Mn/NaY and Mn/USY were prepared by incipient wetness impregnation, while Mn-USY was obtained by hydrothermal synthesis. Mn-USY contained a greater ratio of Mn2+ than Mn/NaY, and Mn/USY. Mn oxides loaded on Y zeolites promoted the COP efficiencies. Mn/NaY increased total organic carbon removal in COP by 7.3% compared to NaY, while Mn/USY and Mn-USY increased 11.5 and 15.8%, respectively, relative to USY in COP. Multivalent Mn oxides (Mn2+, Mn3+, and Mn4+) were highly dispersed on the surface of NaY or USY, and function as catalytic active sites, increasing mineralization. Mn-USY showed the highest total organic carbon removal (44.3%) in COP among the three catalysts, because Mn-USY had a higher ratio of Mn2+ to the total Mn oxides on the surface than Mn/NaY and Mn/USY and the catalytic effects from intercorrelations between Mn oxides and mesoporous surface structures. The hydroxyl radicals and superoxide radicals governed oxidations in COP using Mn-USY. Nitrobenzene was oxidized to polyhydroxy phenol, polyhydroxy nitrophenol, and p-benzoquinone. The intermediates were then oxidized to small organic acids and ultimately carbon dioxide and water. This study demonstrates the potential of Y zeolites used in COP for the treatment of refractory chemical wastewaters.
topic ozonation
catalytic ozonation
Y zeolites
Mn oxides
wastewater treatment
url https://www.frontiersin.org/article/10.3389/fchem.2020.00080/full
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AT yifanli catalyticozonationofnitrobenzenebymanganesebasedyzeolites
AT yalizhan catalyticozonationofnitrobenzenebymanganesebasedyzeolites
AT qinghongwang catalyticozonationofnitrobenzenebymanganesebasedyzeolites
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AT shaohuiguo catalyticozonationofnitrobenzenebymanganesebasedyzeolites
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