The behavior of ozone on different iron oxides surface sites in water

Abstract A transformation process of ozone on different iron oxides suspensions, including α-Fe2O3, α-FeOOH, Fe3O4, was carried out using FTIR of adsorbed pyridine, ATR-FTIR and electron paramagnetic resonance (EPR) spectra with isotope 18O3. It was verified that on the surface isolated hydroxyl gro...

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Autores principales: Liqiang Yan, Jishuai Bing, Hecheng Wu
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Lenguaje:EN
Publicado: Nature Portfolio 2019
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Acceso en línea:https://doaj.org/article/944bf24d7b614199873d94237110c62a
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spelling oai:doaj.org-article:944bf24d7b614199873d94237110c62a2021-12-02T15:09:57ZThe behavior of ozone on different iron oxides surface sites in water10.1038/s41598-019-50910-w2045-2322https://doaj.org/article/944bf24d7b614199873d94237110c62a2019-10-01T00:00:00Zhttps://doi.org/10.1038/s41598-019-50910-whttps://doaj.org/toc/2045-2322Abstract A transformation process of ozone on different iron oxides suspensions, including α-Fe2O3, α-FeOOH, Fe3O4, was carried out using FTIR of adsorbed pyridine, ATR-FTIR and electron paramagnetic resonance (EPR) spectra with isotope 18O3. It was verified that on the surface isolated hydroxyl groups and the surface hydroxyl groups without acid sites of these iron oxides, ozone was electrostatically adsorbed and did not interact with the surface of these oxides, stably existed as ozone molecule. In contrast, ozone could replace the surface hydroxyl groups on Lewis acid sites of oxides, and directly interacted with the surface metal ions, decomposing into reactive oxygen species (ROS) and initiating the surface metal redox. The results indicate that Lewis acid sites were active center while the electronic cycle of the Fe2+/Fe3+ is advantageous to promote ozone decomposition into O2 •− and •OH radicals. The mechanism of catalytic ozonation in different surface acid sites of iron oxides aqueous suspension was proposed on the basis of all experimental information.Liqiang YanJishuai BingHecheng WuNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 9, Iss 1, Pp 1-10 (2019)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Liqiang Yan
Jishuai Bing
Hecheng Wu
The behavior of ozone on different iron oxides surface sites in water
description Abstract A transformation process of ozone on different iron oxides suspensions, including α-Fe2O3, α-FeOOH, Fe3O4, was carried out using FTIR of adsorbed pyridine, ATR-FTIR and electron paramagnetic resonance (EPR) spectra with isotope 18O3. It was verified that on the surface isolated hydroxyl groups and the surface hydroxyl groups without acid sites of these iron oxides, ozone was electrostatically adsorbed and did not interact with the surface of these oxides, stably existed as ozone molecule. In contrast, ozone could replace the surface hydroxyl groups on Lewis acid sites of oxides, and directly interacted with the surface metal ions, decomposing into reactive oxygen species (ROS) and initiating the surface metal redox. The results indicate that Lewis acid sites were active center while the electronic cycle of the Fe2+/Fe3+ is advantageous to promote ozone decomposition into O2 •− and •OH radicals. The mechanism of catalytic ozonation in different surface acid sites of iron oxides aqueous suspension was proposed on the basis of all experimental information.
format article
author Liqiang Yan
Jishuai Bing
Hecheng Wu
author_facet Liqiang Yan
Jishuai Bing
Hecheng Wu
author_sort Liqiang Yan
title The behavior of ozone on different iron oxides surface sites in water
title_short The behavior of ozone on different iron oxides surface sites in water
title_full The behavior of ozone on different iron oxides surface sites in water
title_fullStr The behavior of ozone on different iron oxides surface sites in water
title_full_unstemmed The behavior of ozone on different iron oxides surface sites in water
title_sort behavior of ozone on different iron oxides surface sites in water
publisher Nature Portfolio
publishDate 2019
url https://doaj.org/article/944bf24d7b614199873d94237110c62a
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AT hechengwu thebehaviorofozoneondifferentironoxidessurfacesitesinwater
AT liqiangyan behaviorofozoneondifferentironoxidessurfacesitesinwater
AT jishuaibing behaviorofozoneondifferentironoxidessurfacesitesinwater
AT hechengwu behaviorofozoneondifferentironoxidessurfacesitesinwater
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