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Activation of Peroxymonosulfate by Oxygen Vacancies-Enriched Cobalt-Doped Black TiO(2) Nanotubes for the Removal of Organic Pollutants
[Image: see text] Cobalt-mediated activation of peroxymonosulfate (PMS) has been widely investigated for the oxidation of organic pollutants. Herein, we employ cobalt-doped Black TiO(2) nanotubes (Co-Black TNT) for the efficient, stable, and reusable activator of PMS for the degradation of organic p...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6587153/ https://www.ncbi.nlm.nih.gov/pubmed/31091080 http://dx.doi.org/10.1021/acs.est.9b01449 |
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author | Lim, Jonghun Yang, Yang Hoffmann, Michael R. |
author_facet | Lim, Jonghun Yang, Yang Hoffmann, Michael R. |
author_sort | Lim, Jonghun |
collection | PubMed |
description | [Image: see text] Cobalt-mediated activation of peroxymonosulfate (PMS) has been widely investigated for the oxidation of organic pollutants. Herein, we employ cobalt-doped Black TiO(2) nanotubes (Co-Black TNT) for the efficient, stable, and reusable activator of PMS for the degradation of organic pollutants. Co-Black TNTs induce the activation of PMS by itself and stabilized oxygen vacancies that enhance the bonding with PMS and provide catalytic active sites for PMS activation. A relatively high electronic conductivity associated with the coexistence of Ti(4+) and Ti(3+) in Co-Black TNT enables an efficient electron transfer between PMS and the catalyst. As a result, Co-Black TNT is an effective catalyst for PMS activation, leading to the degradation of selected organic pollutants when compared to other TNTs (TNT, Co-TNT, and Black TNT) and other Co-based materials (Co(3)O(4), Co-TiO(2), CoFe(2)O(4), and Co(3)O(4)/rGO). The observed organic compound degradation kinetics are retarded in the presence of methanol and natural organic matter as sulfate radical scavengers. These results demonstrate that sulfate radical is the primary oxidant generated via PMS activation on Co-Black TNT. The strong interaction between Co and TiO(2) through Co–O–Ti bonds and rapid redox cycle of Co(2+)/Co(3+) in Co-Black TNT prevents cobalt leaching and enhances catalyst stability over a wide pH range and repetitive uses of the catalyst. Electrode-supported Co-Black TNT facilitates the recovery of the catalyst from the treated water. |
format | Online Article Text |
id | pubmed-6587153 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-65871532019-06-24 Activation of Peroxymonosulfate by Oxygen Vacancies-Enriched Cobalt-Doped Black TiO(2) Nanotubes for the Removal of Organic Pollutants Lim, Jonghun Yang, Yang Hoffmann, Michael R. Environ Sci Technol [Image: see text] Cobalt-mediated activation of peroxymonosulfate (PMS) has been widely investigated for the oxidation of organic pollutants. Herein, we employ cobalt-doped Black TiO(2) nanotubes (Co-Black TNT) for the efficient, stable, and reusable activator of PMS for the degradation of organic pollutants. Co-Black TNTs induce the activation of PMS by itself and stabilized oxygen vacancies that enhance the bonding with PMS and provide catalytic active sites for PMS activation. A relatively high electronic conductivity associated with the coexistence of Ti(4+) and Ti(3+) in Co-Black TNT enables an efficient electron transfer between PMS and the catalyst. As a result, Co-Black TNT is an effective catalyst for PMS activation, leading to the degradation of selected organic pollutants when compared to other TNTs (TNT, Co-TNT, and Black TNT) and other Co-based materials (Co(3)O(4), Co-TiO(2), CoFe(2)O(4), and Co(3)O(4)/rGO). The observed organic compound degradation kinetics are retarded in the presence of methanol and natural organic matter as sulfate radical scavengers. These results demonstrate that sulfate radical is the primary oxidant generated via PMS activation on Co-Black TNT. The strong interaction between Co and TiO(2) through Co–O–Ti bonds and rapid redox cycle of Co(2+)/Co(3+) in Co-Black TNT prevents cobalt leaching and enhances catalyst stability over a wide pH range and repetitive uses of the catalyst. Electrode-supported Co-Black TNT facilitates the recovery of the catalyst from the treated water. American Chemical Society 2019-05-15 2019-06-18 /pmc/articles/PMC6587153/ /pubmed/31091080 http://dx.doi.org/10.1021/acs.est.9b01449 Text en Copyright © 2019 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Lim, Jonghun Yang, Yang Hoffmann, Michael R. Activation of Peroxymonosulfate by Oxygen Vacancies-Enriched Cobalt-Doped Black TiO(2) Nanotubes for the Removal of Organic Pollutants |
title | Activation
of Peroxymonosulfate by Oxygen Vacancies-Enriched
Cobalt-Doped Black TiO(2) Nanotubes for the Removal of Organic
Pollutants |
title_full | Activation
of Peroxymonosulfate by Oxygen Vacancies-Enriched
Cobalt-Doped Black TiO(2) Nanotubes for the Removal of Organic
Pollutants |
title_fullStr | Activation
of Peroxymonosulfate by Oxygen Vacancies-Enriched
Cobalt-Doped Black TiO(2) Nanotubes for the Removal of Organic
Pollutants |
title_full_unstemmed | Activation
of Peroxymonosulfate by Oxygen Vacancies-Enriched
Cobalt-Doped Black TiO(2) Nanotubes for the Removal of Organic
Pollutants |
title_short | Activation
of Peroxymonosulfate by Oxygen Vacancies-Enriched
Cobalt-Doped Black TiO(2) Nanotubes for the Removal of Organic
Pollutants |
title_sort | activation
of peroxymonosulfate by oxygen vacancies-enriched
cobalt-doped black tio(2) nanotubes for the removal of organic
pollutants |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6587153/ https://www.ncbi.nlm.nih.gov/pubmed/31091080 http://dx.doi.org/10.1021/acs.est.9b01449 |
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