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Exploring electrochemical mechanisms for clindamycin degradation targeted at the efficient treatment of contaminated water

dc.contributor.authorFaria, Julia
dc.contributor.authorSantacruz, William
dc.contributor.authorDe Mello, Rodrigo [UNESP]
dc.contributor.authorBoldrin, Maria Valnice [UNESP]
dc.contributor.authorMotheo, Artur J.
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.date.accessioned2025-04-29T19:34:50Z
dc.date.issued2024-10-01
dc.description.abstractNumerous studies reveal pollutants like clindamycin (CLD) in the environment, posing environmental and health risks. Conventional water treatment methods are ineffective at removing these contaminants, typically found in low concentrations. An innovative treatment approach is introduced through pre-concentration via adsorption, which is highly efficient, energy-saving, and reusable. The innovation uses solvents like methanol or ethanol to desorb pollutants, creating concentrated CLD solutions for more effective electrochemical degradation than conventional methods. Thus, this study explores, for the first time, the behavior of CLD electro-oxidation in different media—water, methanol, and ethanol—using a Dimensionally Stable Anode (DSA®-Cl₂). The study reveals distinct degradation mechanisms and offers new insights into solvent-assisted electrochemical treatments. After 30 min of electrolysis, all the current densities evaluated promoted significant degradation, ranging from 90 to 92%. The energy consumption was 2.9 Wh m⁻³ per percentage point at current densities of 2 and 3.5 mA cm⁻2. This demonstrates that using higher current densities over shorter electrolysis times is feasible, achieving removal rates of approximately 90%.The performance of chloride-based electrolytes was superior to that of sulfate-based electrolytes due to the ability of DSA®-Cl2 electrodes to generate reactive chlorine species more efficiently. A higher concentration of supporting electrolytes initially improved CLD removal, but no significant changes were observed after 1 h. Neutral pH conditions optimized CLD degradation, achieving up to 91% removal. Higher pollutant concentrations were associated with lower kinetic constants and decreased removal percentages. Methanol and ethanol enhanced removal rates to 98.3% and 92.3%, respectively, by generating oxidizing species such as methoxy, hydroxymethyl, and ethoxy radicals. The degradation by-products differed across the three media, with each solvent exhibiting distinct oxidation mechanisms. These findings highlight the potential of using methanol or ethanol as an electrolytic medium with efficiency comparable to water.en
dc.description.affiliationUniversity of São Paulo (USP) São Carlos Institute of Chemistry, SP
dc.description.affiliationSão Paulo State University (UNESP) Institute of Chemistry Araraquara. Center of Alternative Technologies for Detection Toxicological Evaluation and Removal of Micropollutants and Radioactives (INCT-DATREM) UNESP
dc.description.affiliationUnespSão Paulo State University (UNESP) Institute of Chemistry Araraquara. Center of Alternative Technologies for Detection Toxicological Evaluation and Removal of Micropollutants and Radioactives (INCT-DATREM) UNESP
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.identifierhttp://dx.doi.org/10.1016/j.chemosphere.2024.143563
dc.identifier.citationChemosphere, v. 366.
dc.identifier.doi10.1016/j.chemosphere.2024.143563
dc.identifier.issn1879-1298
dc.identifier.issn0045-6535
dc.identifier.scopus2-s2.0-85206700731
dc.identifier.urihttps://hdl.handle.net/11449/304400
dc.language.isoeng
dc.relation.ispartofChemosphere
dc.sourceScopus
dc.subjectDegradation
dc.subjectElectrochemical oxidation
dc.subjectPreconcentration
dc.subjectWater treatment
dc.titleExploring electrochemical mechanisms for clindamycin degradation targeted at the efficient treatment of contaminated wateren
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublicationbc74a1ce-4c4c-4dad-8378-83962d76c4fd
relation.isOrgUnitOfPublication.latestForDiscoverybc74a1ce-4c4c-4dad-8378-83962d76c4fd
unesp.author.orcid0000-0001-8696-3681[1]
unesp.author.orcid0000-0001-8880-270X[2]
unesp.author.orcid0000-0001-9144-8270[3]
unesp.author.orcid0000-0001-5819-9516[5]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt

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