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Materials Based on Co, Cu, and Cr as Activators of PMS for Degrading a Representative Antibiotic—The Strategy for Utilization in Water Treatment and Warnings on Metal Leaching
A chromate of copper and cobalt (Φy) was synthesized and characterized. Φy activated peroxymonosulfate (PMS) to degrade ciprofloxacin (CIP) in water. The Φy/PMS combination showed a high degrading capability toward CIP (~100% elimination in 15 min). However, Φy leached cobalt (1.6 mg L(−1)), limitin...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10254359/ https://www.ncbi.nlm.nih.gov/pubmed/37299012 http://dx.doi.org/10.3390/molecules28114536 |
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author | Serna-Galvis, Efraím A. Mendoza-Merlano, Carlos Torres-Palma, Ricardo A. Echavarría-Isaza, Adriana Hoyos-Ayala, Dora A. |
author_facet | Serna-Galvis, Efraím A. Mendoza-Merlano, Carlos Torres-Palma, Ricardo A. Echavarría-Isaza, Adriana Hoyos-Ayala, Dora A. |
author_sort | Serna-Galvis, Efraím A. |
collection | PubMed |
description | A chromate of copper and cobalt (Φy) was synthesized and characterized. Φy activated peroxymonosulfate (PMS) to degrade ciprofloxacin (CIP) in water. The Φy/PMS combination showed a high degrading capability toward CIP (~100% elimination in 15 min). However, Φy leached cobalt (1.6 mg L(−1)), limiting its use for water treatment. To avoid leaching, Φy was calcinated, forming a mixed metal oxide (MMO). In the combination of MMO/PMS, no metals leached, the CIP adsorption was low (<20%), and the action of SO(4)•(−) dominated, leading to a synergistic effect on pollutant elimination (>95% after 15 min of treatment). MMO/PMS promoted the opening and oxidation of the piperazyl ring, plus the hydroxylation of the quinolone moiety on CIP, which potentially decreased the biological activity. After three reuse cycles, the MMO still presented with a high activation of PMS toward CIP degradation (90% in 15 min of action). Additionally, the CIP degradation by the MMO/PMS system in simulated hospital wastewater was close to that obtained in distilled water. This work provides relevant information on the stability of Co-, Cu-, and Cr-based materials under interaction with PMS and the strategies to obtain a proper catalyst to degrade CIP. |
format | Online Article Text |
id | pubmed-10254359 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-102543592023-06-10 Materials Based on Co, Cu, and Cr as Activators of PMS for Degrading a Representative Antibiotic—The Strategy for Utilization in Water Treatment and Warnings on Metal Leaching Serna-Galvis, Efraím A. Mendoza-Merlano, Carlos Torres-Palma, Ricardo A. Echavarría-Isaza, Adriana Hoyos-Ayala, Dora A. Molecules Article A chromate of copper and cobalt (Φy) was synthesized and characterized. Φy activated peroxymonosulfate (PMS) to degrade ciprofloxacin (CIP) in water. The Φy/PMS combination showed a high degrading capability toward CIP (~100% elimination in 15 min). However, Φy leached cobalt (1.6 mg L(−1)), limiting its use for water treatment. To avoid leaching, Φy was calcinated, forming a mixed metal oxide (MMO). In the combination of MMO/PMS, no metals leached, the CIP adsorption was low (<20%), and the action of SO(4)•(−) dominated, leading to a synergistic effect on pollutant elimination (>95% after 15 min of treatment). MMO/PMS promoted the opening and oxidation of the piperazyl ring, plus the hydroxylation of the quinolone moiety on CIP, which potentially decreased the biological activity. After three reuse cycles, the MMO still presented with a high activation of PMS toward CIP degradation (90% in 15 min of action). Additionally, the CIP degradation by the MMO/PMS system in simulated hospital wastewater was close to that obtained in distilled water. This work provides relevant information on the stability of Co-, Cu-, and Cr-based materials under interaction with PMS and the strategies to obtain a proper catalyst to degrade CIP. MDPI 2023-06-03 /pmc/articles/PMC10254359/ /pubmed/37299012 http://dx.doi.org/10.3390/molecules28114536 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Serna-Galvis, Efraím A. Mendoza-Merlano, Carlos Torres-Palma, Ricardo A. Echavarría-Isaza, Adriana Hoyos-Ayala, Dora A. Materials Based on Co, Cu, and Cr as Activators of PMS for Degrading a Representative Antibiotic—The Strategy for Utilization in Water Treatment and Warnings on Metal Leaching |
title | Materials Based on Co, Cu, and Cr as Activators of PMS for Degrading a Representative Antibiotic—The Strategy for Utilization in Water Treatment and Warnings on Metal Leaching |
title_full | Materials Based on Co, Cu, and Cr as Activators of PMS for Degrading a Representative Antibiotic—The Strategy for Utilization in Water Treatment and Warnings on Metal Leaching |
title_fullStr | Materials Based on Co, Cu, and Cr as Activators of PMS for Degrading a Representative Antibiotic—The Strategy for Utilization in Water Treatment and Warnings on Metal Leaching |
title_full_unstemmed | Materials Based on Co, Cu, and Cr as Activators of PMS for Degrading a Representative Antibiotic—The Strategy for Utilization in Water Treatment and Warnings on Metal Leaching |
title_short | Materials Based on Co, Cu, and Cr as Activators of PMS for Degrading a Representative Antibiotic—The Strategy for Utilization in Water Treatment and Warnings on Metal Leaching |
title_sort | materials based on co, cu, and cr as activators of pms for degrading a representative antibiotic—the strategy for utilization in water treatment and warnings on metal leaching |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10254359/ https://www.ncbi.nlm.nih.gov/pubmed/37299012 http://dx.doi.org/10.3390/molecules28114536 |
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