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Ca(OH)(2)-mediated activation of peroxymonosulfate for the degradation of bisphenol S
Alkaline substances could activate peroxymonosulfate (PMS) for the removal of organic pollutants, but relatively high alkali consumption is generally required, which can cause too high pH of the solution after the reaction and lead to secondary pollution. Within this study, PMS activated by a relati...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9042291/ https://www.ncbi.nlm.nih.gov/pubmed/35497526 http://dx.doi.org/10.1039/d1ra05286a |
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author | Wu, Leliang Lin, Yiting Zhang, Yimin Wang, Peng Ding, Mingjun Nie, Minghua Yan, Caixia Chen, Shiyao |
author_facet | Wu, Leliang Lin, Yiting Zhang, Yimin Wang, Peng Ding, Mingjun Nie, Minghua Yan, Caixia Chen, Shiyao |
author_sort | Wu, Leliang |
collection | PubMed |
description | Alkaline substances could activate peroxymonosulfate (PMS) for the removal of organic pollutants, but relatively high alkali consumption is generally required, which can cause too high pH of the solution after the reaction and lead to secondary pollution. Within this study, PMS activated by a relatively low dosage of Ca(OH)(2) (1 mM) exhibited excellent efficiency in the removal of bisphenol S (BPS). The pH of the solution declined to almost neutral (pH = 8.2) during the reaction period and conformed to the direct emission standards (pH = 6–9). In a typical case, BPS was completely degraded within 240 min and followed the kinetics of pseudo-first-order. The degradation efficiency of BPS depended on the operating parameters, such as the Ca(OH)(2), PMS and BPS dosages, initial solution pH, reaction temperature, co-existing anions, humic acid (HA), and water matrices. Quenching experiments were performed to verify that singlet oxygen ((1)O(2)) and superoxide radicals (O(2)˙(−)) were the predominant ROS. Degradation of BPS has been significantly accelerated as the temperature increased. Furthermore, degradation of BPS could be maintained at a high level across a broad range of pH values (5.3–11.15). The SO(4)(−), NO(3)(−) did not significantly impact the degradation of BPS, however, both HCO(3)(−) and HA inhibited oxidation of BPS by the Ca(OH)(2)/PMS system, and Cl(−) had a dual-edged sword effect on BPS degradation. In addition, based on the 4 identified intermediates, 3 pathways of BPS degradation were proposed. The degradation of BPS was lower in domestic wastewater compared to other naturals waters and ultrapure; nevertheless, up to 75.86%, 77.94% and 81.48% of BPS was degraded in domestic wastewater, Yaohu Lake water and Poyang Lake water, respectively. Finally, phenolic chemicals and antibiotics, including bisphenol A, norfloxacin, lomefloxacin hydrochloride, and sulfadiazine could also be efficiently removed via the Ca(OH)(2)/PMS system. |
format | Online Article Text |
id | pubmed-9042291 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90422912022-04-28 Ca(OH)(2)-mediated activation of peroxymonosulfate for the degradation of bisphenol S Wu, Leliang Lin, Yiting Zhang, Yimin Wang, Peng Ding, Mingjun Nie, Minghua Yan, Caixia Chen, Shiyao RSC Adv Chemistry Alkaline substances could activate peroxymonosulfate (PMS) for the removal of organic pollutants, but relatively high alkali consumption is generally required, which can cause too high pH of the solution after the reaction and lead to secondary pollution. Within this study, PMS activated by a relatively low dosage of Ca(OH)(2) (1 mM) exhibited excellent efficiency in the removal of bisphenol S (BPS). The pH of the solution declined to almost neutral (pH = 8.2) during the reaction period and conformed to the direct emission standards (pH = 6–9). In a typical case, BPS was completely degraded within 240 min and followed the kinetics of pseudo-first-order. The degradation efficiency of BPS depended on the operating parameters, such as the Ca(OH)(2), PMS and BPS dosages, initial solution pH, reaction temperature, co-existing anions, humic acid (HA), and water matrices. Quenching experiments were performed to verify that singlet oxygen ((1)O(2)) and superoxide radicals (O(2)˙(−)) were the predominant ROS. Degradation of BPS has been significantly accelerated as the temperature increased. Furthermore, degradation of BPS could be maintained at a high level across a broad range of pH values (5.3–11.15). The SO(4)(−), NO(3)(−) did not significantly impact the degradation of BPS, however, both HCO(3)(−) and HA inhibited oxidation of BPS by the Ca(OH)(2)/PMS system, and Cl(−) had a dual-edged sword effect on BPS degradation. In addition, based on the 4 identified intermediates, 3 pathways of BPS degradation were proposed. The degradation of BPS was lower in domestic wastewater compared to other naturals waters and ultrapure; nevertheless, up to 75.86%, 77.94% and 81.48% of BPS was degraded in domestic wastewater, Yaohu Lake water and Poyang Lake water, respectively. Finally, phenolic chemicals and antibiotics, including bisphenol A, norfloxacin, lomefloxacin hydrochloride, and sulfadiazine could also be efficiently removed via the Ca(OH)(2)/PMS system. The Royal Society of Chemistry 2021-10-14 /pmc/articles/PMC9042291/ /pubmed/35497526 http://dx.doi.org/10.1039/d1ra05286a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Wu, Leliang Lin, Yiting Zhang, Yimin Wang, Peng Ding, Mingjun Nie, Minghua Yan, Caixia Chen, Shiyao Ca(OH)(2)-mediated activation of peroxymonosulfate for the degradation of bisphenol S |
title | Ca(OH)(2)-mediated activation of peroxymonosulfate for the degradation of bisphenol S |
title_full | Ca(OH)(2)-mediated activation of peroxymonosulfate for the degradation of bisphenol S |
title_fullStr | Ca(OH)(2)-mediated activation of peroxymonosulfate for the degradation of bisphenol S |
title_full_unstemmed | Ca(OH)(2)-mediated activation of peroxymonosulfate for the degradation of bisphenol S |
title_short | Ca(OH)(2)-mediated activation of peroxymonosulfate for the degradation of bisphenol S |
title_sort | ca(oh)(2)-mediated activation of peroxymonosulfate for the degradation of bisphenol s |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9042291/ https://www.ncbi.nlm.nih.gov/pubmed/35497526 http://dx.doi.org/10.1039/d1ra05286a |
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