Enhanced Activation of Peroxymonosulfate for Tetracycline Degradation Using CoNi-Based Electrodeposited Films
Synthesizing efficient heterogeneous catalysts with multiple active sites able to activate peroxymonosulfate (PMS) for the degradation of persistent organic pollutants continues to be a challenge for societies worldwide. In response, cost-effective, eco-friendly oxidized Ni-rich and Co-rich CoNi mic...
| Authors: | , , , |
|---|---|
| Format: | article |
| Status: | Published version |
| Publication Date: | 2023 |
| Country: | España |
| Institution: | Consejo Superior de Investigaciones Científicas (CSIC) |
| Repository: | DIGITAL.CSIC. Repositorio Institucional del CSIC |
| OAI Identifier: | oai:digital.csic.es:10261/296668 |
| Online Access: | http://hdl.handle.net/10261/296668 |
| Access Level: | Open access |
| Keyword: | CoNi Electrodeposition PMS Sulfate radicals Heterogeneous catalysis Tetracycline Water treatment |
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Enhanced Activation of Peroxymonosulfate for Tetracycline Degradation Using CoNi-Based Electrodeposited FilmsGómez, ElviraFons, ArnauCestaro, RobertoSerrà, AlbertCoNiElectrodepositionPMSSulfate radicalsHeterogeneous catalysisTetracyclineWater treatmentSynthesizing efficient heterogeneous catalysts with multiple active sites able to activate peroxymonosulfate (PMS) for the degradation of persistent organic pollutants continues to be a challenge for societies worldwide. In response, cost-effective, eco-friendly oxidized Ni-rich and Co-rich CoNi micro-nanostructured films were fabricated following a two-step process based on simple electrodeposition using green deep eutectic solvent as an electrochemical media and thermal annealing. The CoNi-based catalysts demonstrated exceptional efficiency in the heterogeneous catalyzed activation of PMS for tetracycline degradation and mineralization. The effects of the catalysts’ chemical nature and morphology, the pH, the concentration of PMS, irradiation with visible light, and the duration of contact with the catalysts on the degradation and mineralization of tetracycline were also studied. In dark conditions, oxidized Co-rich CoNi degraded more than 99% of tetracyclines in only 30 min and mineralized more than 99% of them in only 60 min. Moreover, the degradation kinetics doubled from 0.173 min−1 in dark conditions to 0.388 min−1 under visible light irradiation. In addition, the material demonstrated excellent reusability and can be easily recovered with simple heat treatment. Given those findings, our work provides new strategies for constructing high-efficiency and cost-effective PMS catalysts and elucidating the effects of operational parameters and primary reactive species formed by the catalyst–PMS system on water treatment technologies.This research was funded by Grant PID2020-115663GB-C32 funded by MCIN/AEI/10.13039/501100011033.Peer reviewedMultidisciplinary Digital Publishing InstituteMinisterio de Ciencia, Innovación y Universidades (España)Agencia Estatal de Investigación (España)Consejo Superior de Investigaciones Científicas [https://ror.org/02gfc7t72]2023202320232023info:eu-repo/semantics/articlehttp://purl.org/coar/resource_type/c_6501Publisher's versioninfo:eu-repo/semantics/publishedVersionapplication/pdfhttp://hdl.handle.net/10261/296668reponame:DIGITAL.CSIC. Repositorio Institucional del CSICinstname:Consejo Superior de Investigaciones Científicas (CSIC)Inglés#PLACEHOLDER_PARENT_METADATA_VALUE#info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2020-115663GB-C32https://doi.org/10.3390/nano13050790Síinfo:eu-repo/semantics/openAccessoai:digital.csic.es:10261/2966682026-05-22T06:33:51Z |
| dc.title.none.fl_str_mv |
Enhanced Activation of Peroxymonosulfate for Tetracycline Degradation Using CoNi-Based Electrodeposited Films |
| title |
Enhanced Activation of Peroxymonosulfate for Tetracycline Degradation Using CoNi-Based Electrodeposited Films |
| spellingShingle |
Enhanced Activation of Peroxymonosulfate for Tetracycline Degradation Using CoNi-Based Electrodeposited Films Gómez, Elvira CoNi Electrodeposition PMS Sulfate radicals Heterogeneous catalysis Tetracycline Water treatment |
| title_short |
Enhanced Activation of Peroxymonosulfate for Tetracycline Degradation Using CoNi-Based Electrodeposited Films |
| title_full |
Enhanced Activation of Peroxymonosulfate for Tetracycline Degradation Using CoNi-Based Electrodeposited Films |
| title_fullStr |
Enhanced Activation of Peroxymonosulfate for Tetracycline Degradation Using CoNi-Based Electrodeposited Films |
| title_full_unstemmed |
Enhanced Activation of Peroxymonosulfate for Tetracycline Degradation Using CoNi-Based Electrodeposited Films |
| title_sort |
Enhanced Activation of Peroxymonosulfate for Tetracycline Degradation Using CoNi-Based Electrodeposited Films |
| dc.creator.none.fl_str_mv |
Gómez, Elvira Fons, Arnau Cestaro, Roberto Serrà, Albert |
| author |
Gómez, Elvira |
| author_facet |
Gómez, Elvira Fons, Arnau Cestaro, Roberto Serrà, Albert |
| author_role |
author |
| author2 |
Fons, Arnau Cestaro, Roberto Serrà, Albert |
| author2_role |
author author author |
| dc.contributor.none.fl_str_mv |
Ministerio de Ciencia, Innovación y Universidades (España) Agencia Estatal de Investigación (España) Consejo Superior de Investigaciones Científicas [https://ror.org/02gfc7t72] |
| dc.subject.none.fl_str_mv |
CoNi Electrodeposition PMS Sulfate radicals Heterogeneous catalysis Tetracycline Water treatment |
| topic |
CoNi Electrodeposition PMS Sulfate radicals Heterogeneous catalysis Tetracycline Water treatment |
| description |
Synthesizing efficient heterogeneous catalysts with multiple active sites able to activate peroxymonosulfate (PMS) for the degradation of persistent organic pollutants continues to be a challenge for societies worldwide. In response, cost-effective, eco-friendly oxidized Ni-rich and Co-rich CoNi micro-nanostructured films were fabricated following a two-step process based on simple electrodeposition using green deep eutectic solvent as an electrochemical media and thermal annealing. The CoNi-based catalysts demonstrated exceptional efficiency in the heterogeneous catalyzed activation of PMS for tetracycline degradation and mineralization. The effects of the catalysts’ chemical nature and morphology, the pH, the concentration of PMS, irradiation with visible light, and the duration of contact with the catalysts on the degradation and mineralization of tetracycline were also studied. In dark conditions, oxidized Co-rich CoNi degraded more than 99% of tetracyclines in only 30 min and mineralized more than 99% of them in only 60 min. Moreover, the degradation kinetics doubled from 0.173 min−1 in dark conditions to 0.388 min−1 under visible light irradiation. In addition, the material demonstrated excellent reusability and can be easily recovered with simple heat treatment. Given those findings, our work provides new strategies for constructing high-efficiency and cost-effective PMS catalysts and elucidating the effects of operational parameters and primary reactive species formed by the catalyst–PMS system on water treatment technologies. |
| publishDate |
2023 |
| dc.date.none.fl_str_mv |
2023 2023 2023 2023 |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article http://purl.org/coar/resource_type/c_6501 Publisher's version info:eu-repo/semantics/publishedVersion |
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article |
| status_str |
publishedVersion |
| dc.identifier.none.fl_str_mv |
http://hdl.handle.net/10261/296668 |
| url |
http://hdl.handle.net/10261/296668 |
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Inglés |
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Inglés |
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#PLACEHOLDER_PARENT_METADATA_VALUE# info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2020-115663GB-C32 https://doi.org/10.3390/nano13050790 Sí |
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info:eu-repo/semantics/openAccess |
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openAccess |
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application/pdf |
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Multidisciplinary Digital Publishing Institute |
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Multidisciplinary Digital Publishing Institute |
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reponame:DIGITAL.CSIC. Repositorio Institucional del CSIC instname:Consejo Superior de Investigaciones Científicas (CSIC) |
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Consejo Superior de Investigaciones Científicas (CSIC) |
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DIGITAL.CSIC. Repositorio Institucional del CSIC |
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DIGITAL.CSIC. Repositorio Institucional del CSIC |
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