Removal of bisphenol A from acidic sulfate medium and urban wastewater using persulfate activated with electroregenerated Fe2+
Model solutions of bisphenol A (BPA) in 0.050 M Na2SO4 at pH 3.0 have been treated by the electro/Fe2+/persulfate process. The activation of 5.0 mM persulfate with 0.20 mM Fe2+ yielded a mixture of sulfate radical anion (SO4*- ) and * OH, although quenching tests revealed the prevalence of the forme...
| Authors: | , , |
|---|---|
| Format: | article |
| Status: | Versión aceptada para publicación |
| Publication Date: | 2020 |
| Country: | España |
| Institution: | Universidad de Barcelona |
| Repository: | Dipòsit Digital de la UB |
| OAI Identifier: | oai:diposit.ub.edu:2445/170748 |
| Online Access: | https://hdl.handle.net/2445/170748 |
| Access Level: | Open access |
| Keyword: | Depuració d'aigües residuals Contaminants emergents en l'aigua Purification of sewage Emerging contaminants in water |
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Removal of bisphenol A from acidic sulfate medium and urban wastewater using persulfate activated with electroregenerated Fe2+Dos Santos, Alexsandro JhonesSirés Sadornil, IgnacioBrillas, EnricDepuració d'aigües residualsContaminants emergents en l'aiguaPurification of sewageEmerging contaminants in waterModel solutions of bisphenol A (BPA) in 0.050 M Na2SO4 at pH 3.0 have been treated by the electro/Fe2+/persulfate process. The activation of 5.0 mM persulfate with 0.20 mM Fe2+ yielded a mixture of sulfate radical anion (SO4*- ) and * OH, although quenching tests revealed the prevalence of the former species as the main oxidizing agent. In trials run in an IrO2/carbon-felt cell, 98.4% degradation was achieved alongside 61.8% mineralization. The energy consumption was 253.9 kWh (kg TOC) -1, becoming more cost-effective as compared to cells with boron-doped diamond and Pt anodes. Carbon felt outperformed stainless steel as cathode because of the faster Fe2+ regeneration. All BPA concentration decays agreed with a pseudo-fist-order kinetics. The effect of persulfate, Fe2+ and BPA concentrations as well as of the applied current on the degradation process was assessed. Two dehydroxylated and three hydroxylated monobenzenic by-products appeared upon SO4*- and * OH attack, respectively. The analogous treatment of BPA spiked into urban wastewater yielded a faster degradation and mineralization due to the cogeneration of HClO and the larger *OH production as SO4*- reacted with Cl- .Elsevier Ltd2020info:eu-repo/semantics/articleinfo:eu-repo/semantics/acceptedVersionapplication/pdfhttps://hdl.handle.net/2445/170748Articles publicats en revistes (Ciència dels Materials i Química Física)reponame:Dipòsit Digital de la UBinstname:Universidad de BarcelonaInglésVersió postprint del document publicat a: https://doi.org/10.1016/j.chemosphere.2020.128271Chemosphere, 2020, vol. 263, num. 128271https://doi.org/10.1016/j.chemosphere.2020.128271cc-by-nc-nd (c) Elsevier Ltd, 2020http://creativecommons.org/licenses/by-nc-nd/3.0/esinfo:eu-repo/semantics/openAccessoai:diposit.ub.edu:2445/1707482026-05-27T06:46:51Z |
| dc.title.none.fl_str_mv |
Removal of bisphenol A from acidic sulfate medium and urban wastewater using persulfate activated with electroregenerated Fe2+ |
| title |
Removal of bisphenol A from acidic sulfate medium and urban wastewater using persulfate activated with electroregenerated Fe2+ |
| spellingShingle |
Removal of bisphenol A from acidic sulfate medium and urban wastewater using persulfate activated with electroregenerated Fe2+ Dos Santos, Alexsandro Jhones Depuració d'aigües residuals Contaminants emergents en l'aigua Purification of sewage Emerging contaminants in water |
| title_short |
Removal of bisphenol A from acidic sulfate medium and urban wastewater using persulfate activated with electroregenerated Fe2+ |
| title_full |
Removal of bisphenol A from acidic sulfate medium and urban wastewater using persulfate activated with electroregenerated Fe2+ |
| title_fullStr |
Removal of bisphenol A from acidic sulfate medium and urban wastewater using persulfate activated with electroregenerated Fe2+ |
| title_full_unstemmed |
Removal of bisphenol A from acidic sulfate medium and urban wastewater using persulfate activated with electroregenerated Fe2+ |
| title_sort |
Removal of bisphenol A from acidic sulfate medium and urban wastewater using persulfate activated with electroregenerated Fe2+ |
| dc.creator.none.fl_str_mv |
Dos Santos, Alexsandro Jhones Sirés Sadornil, Ignacio Brillas, Enric |
| author |
Dos Santos, Alexsandro Jhones |
| author_facet |
Dos Santos, Alexsandro Jhones Sirés Sadornil, Ignacio Brillas, Enric |
| author_role |
author |
| author2 |
Sirés Sadornil, Ignacio Brillas, Enric |
| author2_role |
author author |
| dc.subject.none.fl_str_mv |
Depuració d'aigües residuals Contaminants emergents en l'aigua Purification of sewage Emerging contaminants in water |
| topic |
Depuració d'aigües residuals Contaminants emergents en l'aigua Purification of sewage Emerging contaminants in water |
| description |
Model solutions of bisphenol A (BPA) in 0.050 M Na2SO4 at pH 3.0 have been treated by the electro/Fe2+/persulfate process. The activation of 5.0 mM persulfate with 0.20 mM Fe2+ yielded a mixture of sulfate radical anion (SO4*- ) and * OH, although quenching tests revealed the prevalence of the former species as the main oxidizing agent. In trials run in an IrO2/carbon-felt cell, 98.4% degradation was achieved alongside 61.8% mineralization. The energy consumption was 253.9 kWh (kg TOC) -1, becoming more cost-effective as compared to cells with boron-doped diamond and Pt anodes. Carbon felt outperformed stainless steel as cathode because of the faster Fe2+ regeneration. All BPA concentration decays agreed with a pseudo-fist-order kinetics. The effect of persulfate, Fe2+ and BPA concentrations as well as of the applied current on the degradation process was assessed. Two dehydroxylated and three hydroxylated monobenzenic by-products appeared upon SO4*- and * OH attack, respectively. The analogous treatment of BPA spiked into urban wastewater yielded a faster degradation and mineralization due to the cogeneration of HClO and the larger *OH production as SO4*- reacted with Cl- . |
| publishDate |
2020 |
| dc.date.none.fl_str_mv |
2020 |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/acceptedVersion |
| format |
article |
| status_str |
acceptedVersion |
| dc.identifier.none.fl_str_mv |
https://hdl.handle.net/2445/170748 |
| url |
https://hdl.handle.net/2445/170748 |
| dc.language.none.fl_str_mv |
Inglés |
| language_invalid_str_mv |
Inglés |
| dc.relation.none.fl_str_mv |
Versió postprint del document publicat a: https://doi.org/10.1016/j.chemosphere.2020.128271 Chemosphere, 2020, vol. 263, num. 128271 https://doi.org/10.1016/j.chemosphere.2020.128271 |
| dc.rights.none.fl_str_mv |
cc-by-nc-nd (c) Elsevier Ltd, 2020 http://creativecommons.org/licenses/by-nc-nd/3.0/es info:eu-repo/semantics/openAccess |
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cc-by-nc-nd (c) Elsevier Ltd, 2020 http://creativecommons.org/licenses/by-nc-nd/3.0/es |
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openAccess |
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application/pdf |
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Elsevier Ltd |
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Elsevier Ltd |
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Articles publicats en revistes (Ciència dels Materials i Química Física) reponame:Dipòsit Digital de la UB instname:Universidad de Barcelona |
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Universidad de Barcelona |
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Dipòsit Digital de la UB |
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Dipòsit Digital de la UB |
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15,301629 |