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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Nature Portfolio
2019
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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) |
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Medicine R Science Q Liqiang Yan Jishuai Bing Hecheng Wu The behavior of ozone on different iron oxides surface sites in water |
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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 |
work_keys_str_mv |
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_version_ |
1718387766646013952 |