Integrated-electrochemical approaches powered by photovoltaic energy for detecting and treating paracetamol in water

Detalhes bibliográficos
Autor(a) principal: Henrique, João M.M.
Data de Publicação: 2020
Outros Autores: Monteiro, Mayra K.S., Cardozo, Jussara C., Martínez-Huitle, Carlos A. [UNESP], da Silva, Djalma R., dos Santos, Elisama V. [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.jelechem.2020.114734
http://hdl.handle.net/11449/205251
Resumo: Paracetamol is frequently used as an over-the-counter painkiller and is one of the most commonly consumed pharmaceuticals. Consequently, it is increasingly found in the natural environment, such as the water and soil. For this reason, the monitoring its concentration in water and the treatment of polluted effluents with paracetamol is a key issue to overcome urgently. Then, in this study, an electrochemical measuring device and electrochemical water treatment are integrated for their environmental application on paracetamol control. In the former, raw cork-graphite electrochemical sensor was prepared and a simple differential pulse voltammetric (DPV) method was developed for the quantitative determination of paracetamol. Meanwhile, the degradation of paracetamol was carried out with BDD anode by applying 15, 30, and 60 mA cm−2 and using different electrolyte concentrations of Na2SO4 (25, 50, 75, and 100 mM) over 240 min of treatment, in the latter. The decay and degradation of paracetamol were monitored by DPV, and HPLC measurements. Results indicated that, the electrochemical device exhibited a clear current response, allowing to quantify the analyte in the 2.5–1000 μM range, with limit of detection and quantification of 1.03 μM and 2.44 μM, respectively. Alternatively, BDD-electrolysis demonstrated to be an efficient process for removing organic matter from the pharmaceutical compound effluent via the production of strong oxidizing species. Lower paracetamol concentrations were detected, using the electrochemical sensor, when higher current densities and sulfate concentrations were used in BDD-electrolysis, demonstrating the applicability of integrated-technologies. The evolution of short-carboxylic acids (oxalic, formic, oxamic, maleic, acetic, and glycoxylic) was observed at 60 mA cm−2 and 100 mM of Na2SO4, but all of them were eliminated after 240 min. Inorganic ions (NH4+ and NO3−) were also detected under these experimental conditions, confirming that the pollutant was mineralized. Finally, lower energy requirements were estimated for all experimental conditions; however, solar photovoltaic (PV) renewable energy has been utilized to power these electrochemical technologies, decreasing the investment cost.
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spelling Integrated-electrochemical approaches powered by photovoltaic energy for detecting and treating paracetamol in waterBoron doped diamondCorkElectrochemical technologiesParacetamolRenewable energySensorParacetamol is frequently used as an over-the-counter painkiller and is one of the most commonly consumed pharmaceuticals. Consequently, it is increasingly found in the natural environment, such as the water and soil. For this reason, the monitoring its concentration in water and the treatment of polluted effluents with paracetamol is a key issue to overcome urgently. Then, in this study, an electrochemical measuring device and electrochemical water treatment are integrated for their environmental application on paracetamol control. In the former, raw cork-graphite electrochemical sensor was prepared and a simple differential pulse voltammetric (DPV) method was developed for the quantitative determination of paracetamol. Meanwhile, the degradation of paracetamol was carried out with BDD anode by applying 15, 30, and 60 mA cm−2 and using different electrolyte concentrations of Na2SO4 (25, 50, 75, and 100 mM) over 240 min of treatment, in the latter. The decay and degradation of paracetamol were monitored by DPV, and HPLC measurements. Results indicated that, the electrochemical device exhibited a clear current response, allowing to quantify the analyte in the 2.5–1000 μM range, with limit of detection and quantification of 1.03 μM and 2.44 μM, respectively. Alternatively, BDD-electrolysis demonstrated to be an efficient process for removing organic matter from the pharmaceutical compound effluent via the production of strong oxidizing species. Lower paracetamol concentrations were detected, using the electrochemical sensor, when higher current densities and sulfate concentrations were used in BDD-electrolysis, demonstrating the applicability of integrated-technologies. The evolution of short-carboxylic acids (oxalic, formic, oxamic, maleic, acetic, and glycoxylic) was observed at 60 mA cm−2 and 100 mM of Na2SO4, but all of them were eliminated after 240 min. Inorganic ions (NH4+ and NO3−) were also detected under these experimental conditions, confirming that the pollutant was mineralized. Finally, lower energy requirements were estimated for all experimental conditions; however, solar photovoltaic (PV) renewable energy has been utilized to power these electrochemical technologies, decreasing the investment cost.Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Instituto de Química Universidade Federal do Rio Grande do Norte, CEP 59.072-900National Institute for Alternative Technologies of Detection Toxicological Evaluation and Removal of Micropollutants and Radioactives (INCT-DATREM) Institute of Chemistry UNESP, P.O. Box 355School of Science and Technology Federal University of Rio Grande do Norte Campus Universitario, 59.072-900National Institute for Alternative Technologies of Detection Toxicological Evaluation and Removal of Micropollutants and Radioactives (INCT-DATREM) Institute of Chemistry UNESP, P.O. Box 355CNPq: 306323/2018-4CNPq: 430121/2016-4Universidade Federal do Rio Grande do NorteUniversidade Estadual Paulista (Unesp)Federal University of Rio Grande do NorteHenrique, João M.M.Monteiro, Mayra K.S.Cardozo, Jussara C.Martínez-Huitle, Carlos A. [UNESP]da Silva, Djalma R.dos Santos, Elisama V. [UNESP]2021-06-25T10:12:18Z2021-06-25T10:12:18Z2020-11-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1016/j.jelechem.2020.114734Journal of Electroanalytical Chemistry, v. 876.1572-6657http://hdl.handle.net/11449/20525110.1016/j.jelechem.2020.1147342-s2.0-85092018596Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Electroanalytical Chemistryinfo:eu-repo/semantics/openAccess2021-10-23T12:23:55Zoai:repositorio.unesp.br:11449/205251Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462021-10-23T12:23:55Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Integrated-electrochemical approaches powered by photovoltaic energy for detecting and treating paracetamol in water
title Integrated-electrochemical approaches powered by photovoltaic energy for detecting and treating paracetamol in water
spellingShingle Integrated-electrochemical approaches powered by photovoltaic energy for detecting and treating paracetamol in water
Henrique, João M.M.
Boron doped diamond
Cork
Electrochemical technologies
Paracetamol
Renewable energy
Sensor
title_short Integrated-electrochemical approaches powered by photovoltaic energy for detecting and treating paracetamol in water
title_full Integrated-electrochemical approaches powered by photovoltaic energy for detecting and treating paracetamol in water
title_fullStr Integrated-electrochemical approaches powered by photovoltaic energy for detecting and treating paracetamol in water
title_full_unstemmed Integrated-electrochemical approaches powered by photovoltaic energy for detecting and treating paracetamol in water
title_sort Integrated-electrochemical approaches powered by photovoltaic energy for detecting and treating paracetamol in water
author Henrique, João M.M.
author_facet Henrique, João M.M.
Monteiro, Mayra K.S.
Cardozo, Jussara C.
Martínez-Huitle, Carlos A. [UNESP]
da Silva, Djalma R.
dos Santos, Elisama V. [UNESP]
author_role author
author2 Monteiro, Mayra K.S.
Cardozo, Jussara C.
Martínez-Huitle, Carlos A. [UNESP]
da Silva, Djalma R.
dos Santos, Elisama V. [UNESP]
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal do Rio Grande do Norte
Universidade Estadual Paulista (Unesp)
Federal University of Rio Grande do Norte
dc.contributor.author.fl_str_mv Henrique, João M.M.
Monteiro, Mayra K.S.
Cardozo, Jussara C.
Martínez-Huitle, Carlos A. [UNESP]
da Silva, Djalma R.
dos Santos, Elisama V. [UNESP]
dc.subject.por.fl_str_mv Boron doped diamond
Cork
Electrochemical technologies
Paracetamol
Renewable energy
Sensor
topic Boron doped diamond
Cork
Electrochemical technologies
Paracetamol
Renewable energy
Sensor
description Paracetamol is frequently used as an over-the-counter painkiller and is one of the most commonly consumed pharmaceuticals. Consequently, it is increasingly found in the natural environment, such as the water and soil. For this reason, the monitoring its concentration in water and the treatment of polluted effluents with paracetamol is a key issue to overcome urgently. Then, in this study, an electrochemical measuring device and electrochemical water treatment are integrated for their environmental application on paracetamol control. In the former, raw cork-graphite electrochemical sensor was prepared and a simple differential pulse voltammetric (DPV) method was developed for the quantitative determination of paracetamol. Meanwhile, the degradation of paracetamol was carried out with BDD anode by applying 15, 30, and 60 mA cm−2 and using different electrolyte concentrations of Na2SO4 (25, 50, 75, and 100 mM) over 240 min of treatment, in the latter. The decay and degradation of paracetamol were monitored by DPV, and HPLC measurements. Results indicated that, the electrochemical device exhibited a clear current response, allowing to quantify the analyte in the 2.5–1000 μM range, with limit of detection and quantification of 1.03 μM and 2.44 μM, respectively. Alternatively, BDD-electrolysis demonstrated to be an efficient process for removing organic matter from the pharmaceutical compound effluent via the production of strong oxidizing species. Lower paracetamol concentrations were detected, using the electrochemical sensor, when higher current densities and sulfate concentrations were used in BDD-electrolysis, demonstrating the applicability of integrated-technologies. The evolution of short-carboxylic acids (oxalic, formic, oxamic, maleic, acetic, and glycoxylic) was observed at 60 mA cm−2 and 100 mM of Na2SO4, but all of them were eliminated after 240 min. Inorganic ions (NH4+ and NO3−) were also detected under these experimental conditions, confirming that the pollutant was mineralized. Finally, lower energy requirements were estimated for all experimental conditions; however, solar photovoltaic (PV) renewable energy has been utilized to power these electrochemical technologies, decreasing the investment cost.
publishDate 2020
dc.date.none.fl_str_mv 2020-11-01
2021-06-25T10:12:18Z
2021-06-25T10:12:18Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1016/j.jelechem.2020.114734
Journal of Electroanalytical Chemistry, v. 876.
1572-6657
http://hdl.handle.net/11449/205251
10.1016/j.jelechem.2020.114734
2-s2.0-85092018596
url http://dx.doi.org/10.1016/j.jelechem.2020.114734
http://hdl.handle.net/11449/205251
identifier_str_mv Journal of Electroanalytical Chemistry, v. 876.
1572-6657
10.1016/j.jelechem.2020.114734
2-s2.0-85092018596
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal of Electroanalytical Chemistry
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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