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Ultrafast degradation of SMX and TC by CoSiO(x) activated peroxymonosulfate: efficiency and mechanism

To address the concern about residual antibiotics in effluent of sewage treatment plants, cobalt silicate (CoSiO(x)) was prepared by hydrothermal method and employed as an activator of peroxymonosulfate (PMS) for the rapid degradation of antibiotics. Taking sulfamethoxazole (SMX) and tetracycline (T...

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Autores principales: Liu, Xiaowei, Chen, Chen, Chen, Peng, Wang, Lili
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9854247/
https://www.ncbi.nlm.nih.gov/pubmed/36756404
http://dx.doi.org/10.1039/d2ra06865f
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author Liu, Xiaowei
Chen, Chen
Chen, Peng
Wang, Lili
author_facet Liu, Xiaowei
Chen, Chen
Chen, Peng
Wang, Lili
author_sort Liu, Xiaowei
collection PubMed
description To address the concern about residual antibiotics in effluent of sewage treatment plants, cobalt silicate (CoSiO(x)) was prepared by hydrothermal method and employed as an activator of peroxymonosulfate (PMS) for the rapid degradation of antibiotics. Taking sulfamethoxazole (SMX) and tetracycline (TC) as representatives of antibiotics, the effects of operation parameters (CoSiO(x) and PMS dosage) and water quality parameters (temperature, solution pH, bicarbonate, chloride, and natural organic matter) on degradation of target pollutants by a CoSiO(x) activated PMS process (CoSiO(x)/PMS) were investigated. The mechanism involved in the interaction of CoSiO(x) and PMS was also elucidated. The results indicated that CoSiO(x)/PMS can degrade SMX and TC at fast pseudo-first-order rate constants (0.47 and 0.56 min(−1) respectively) under optimal conditions. Increasing the dosage of PMS and CoSiO(x) appropriately was beneficial to the degradation of antibiotics. Chloride, bicarbonate, and HA showed negative effects on the degradation process due to their free radical-scavenging ability and were ranked as chloride < bicarbonate < HA. Abundant [triple bond, length as m-dash]Co–OH(s) and oxygen vacancies on the surface of CoSiO(x) contributed to its excellent activation capability towards PMS. The radical scavenging experiments indicated that target pollutant degradation mainly resulted from the attack of sulfate radicals (43.0% contribution) and hydroxyl radicals (52.9% contribution). The practicality of CoSiO(x)/PMS was verified by continuous flow test. This study provides a cheap, highly efficient, and feasible advanced depollution method based on CoSiO(x).
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spelling pubmed-98542472023-02-07 Ultrafast degradation of SMX and TC by CoSiO(x) activated peroxymonosulfate: efficiency and mechanism Liu, Xiaowei Chen, Chen Chen, Peng Wang, Lili RSC Adv Chemistry To address the concern about residual antibiotics in effluent of sewage treatment plants, cobalt silicate (CoSiO(x)) was prepared by hydrothermal method and employed as an activator of peroxymonosulfate (PMS) for the rapid degradation of antibiotics. Taking sulfamethoxazole (SMX) and tetracycline (TC) as representatives of antibiotics, the effects of operation parameters (CoSiO(x) and PMS dosage) and water quality parameters (temperature, solution pH, bicarbonate, chloride, and natural organic matter) on degradation of target pollutants by a CoSiO(x) activated PMS process (CoSiO(x)/PMS) were investigated. The mechanism involved in the interaction of CoSiO(x) and PMS was also elucidated. The results indicated that CoSiO(x)/PMS can degrade SMX and TC at fast pseudo-first-order rate constants (0.47 and 0.56 min(−1) respectively) under optimal conditions. Increasing the dosage of PMS and CoSiO(x) appropriately was beneficial to the degradation of antibiotics. Chloride, bicarbonate, and HA showed negative effects on the degradation process due to their free radical-scavenging ability and were ranked as chloride < bicarbonate < HA. Abundant [triple bond, length as m-dash]Co–OH(s) and oxygen vacancies on the surface of CoSiO(x) contributed to its excellent activation capability towards PMS. The radical scavenging experiments indicated that target pollutant degradation mainly resulted from the attack of sulfate radicals (43.0% contribution) and hydroxyl radicals (52.9% contribution). The practicality of CoSiO(x)/PMS was verified by continuous flow test. This study provides a cheap, highly efficient, and feasible advanced depollution method based on CoSiO(x). The Royal Society of Chemistry 2023-01-20 /pmc/articles/PMC9854247/ /pubmed/36756404 http://dx.doi.org/10.1039/d2ra06865f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Liu, Xiaowei
Chen, Chen
Chen, Peng
Wang, Lili
Ultrafast degradation of SMX and TC by CoSiO(x) activated peroxymonosulfate: efficiency and mechanism
title Ultrafast degradation of SMX and TC by CoSiO(x) activated peroxymonosulfate: efficiency and mechanism
title_full Ultrafast degradation of SMX and TC by CoSiO(x) activated peroxymonosulfate: efficiency and mechanism
title_fullStr Ultrafast degradation of SMX and TC by CoSiO(x) activated peroxymonosulfate: efficiency and mechanism
title_full_unstemmed Ultrafast degradation of SMX and TC by CoSiO(x) activated peroxymonosulfate: efficiency and mechanism
title_short Ultrafast degradation of SMX and TC by CoSiO(x) activated peroxymonosulfate: efficiency and mechanism
title_sort ultrafast degradation of smx and tc by cosio(x) activated peroxymonosulfate: efficiency and mechanism
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9854247/
https://www.ncbi.nlm.nih.gov/pubmed/36756404
http://dx.doi.org/10.1039/d2ra06865f
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