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Wet peroxide oxidation of paracetamol using natural clay-based materials as catalysts

dc.contributor.authorSilva, Adriano S.
dc.contributor.authorDíaz de Tuesta, Jose Luis
dc.contributor.authorSgorlon, Juliana
dc.contributor.authorKalmakhanova, Marzhan
dc.contributor.authorGomes, Helder
dc.date.accessioned2020-01-14T15:01:08Z
dc.date.available2020-01-14T15:01:08Z
dc.date.issued2019
dc.description.abstractIn recent years, many pharmaceutical compounds have been identified worldwide at trace levels (in the order from ng·L·1 to mg·L-1) in the aquatic 12nvironment [1]. The presence of pharmaceutical contaminants in water, even at low concentrations, could bring harmful toxicological consequences to human beings and animals that ingested the contaminated water [2]. This work deals with the treatment of water containing paracetamol (PCM) by catalytic wet peroxide oxidation (CWPO) using clay-based materials as catalysts. PCM was considered as a model pharmaceutical emergent pollutant. For the preparation of the catalysts, natural clays from four different regions of Kazakhstan were used Akzhar, Asa, Karatau, and Kokshetau. From the clay obtained in kokshetau deposit, three catalysts were prepared: 1) natural one (KON), 2) calcined clay at 600 °C for 5 h (KOC), and 3) a pillarized clay (KOP) with a pillaring solution containing 0.25 M CoCI2, 0.5 M FeCI3 and 0.5 M NaOH, resulting in OH/(Fe+Co) = 2:1. Additionally, three clays were ptrepared by the same procedure of pillarization from the Akzhar, Asa and Karatau natural clays, resulting in AKP, ASP, and KAP, respectively. The concentration of PCM, H20 2 and total organic carbon (TOC) were followed during the CWPO experiments (Fig. 1 ). All materials revealed high catalytic activity, the non-pillared samples allowing to remove more than 33.4% of PCM after 24 h of reaction time under the following operating conditions: 80 °C, initial pH 3.5, Ccatalyst = 2.5 g L-1, CPCM = 100 mg L-1 and CH202 = 472 mg L-1. The CWPO runs done with the pill a red clay catalysts resulted in more than 90% of removal of the pollutant after 24 h of reaction. The best catalyst was KOP since it leads to the complete removal of the pollutant after 8 h of reaction time and to the highest abatement of TOC (>60%) under the same operational conditions.pt_PT
dc.description.sponsorshipThis work is a result of Project "AIProcMat@N2020 -Advanced lndustrial Processes and Materials for a Sustainable Northern Region of Portugal 2020', with the reference NORTE-01-0145-FEDER-000006, supported by ERDF; and the Associate Laboratory LSRE-LCM UID/EQU/50020/2019 - funded by national funds through FCT/MCTES (PIDDAC); and CIMO - UID/AGR/00690/2019 through FEDERunder Program PT2020.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationSilva, Adriano; Diáz de Tuesta, Jose Luis; Sgorlon, Juliana; Kalmakhanov, Marzhan; Gomes, Helder (2019). Wet peroxide oxidation of paracetamol using natural clay-based materials as catalysts. In XXV Encontro Galego-Português de Química. Santiago de Compostela. ISBN 978-84-09-16320-5pt_PT
dc.identifier.isbn978-84-09-16320-5
dc.identifier.urihttp://hdl.handle.net/10198/20359
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/pt_PT
dc.titleWet peroxide oxidation of paracetamol using natural clay-based materials as catalystspt_PT
dc.typeconference object
dspace.entity.typePublication
oaire.citation.conferencePlaceSantiago de Compostela, Espanhapt_PT
oaire.citation.startPage92pt_PT
oaire.citation.titleXXV Encontro Galego-Portugues de Quimicapt_PT
person.familyNameSilva
person.familyNameDíaz de Tuesta
person.familyNameGomes
person.givenNameAdriano S.
person.givenNameJose Luis
person.givenNameHelder
person.identifier.ciencia-id3E14-5049-B09D
person.identifier.ciencia-id7A1F-022B-7DBF
person.identifier.ciencia-id6218-1E19-13EE
person.identifier.orcid0000-0002-6795-2335
person.identifier.orcid0000-0003-2408-087X
person.identifier.orcid0000-0001-6898-2408
person.identifier.ridD-9785-2017
person.identifier.scopus-author-id55755821600
rcaap.rightsopenAccesspt_PT
rcaap.typeconferenceObjectpt_PT
relation.isAuthorOfPublication3ba90ba4-aac8-4892-a30f-25a10bc27298
relation.isAuthorOfPublication2ad0465f-5f8a-4b14-90f5-bf85996f9ce1
relation.isAuthorOfPublication0eb96337-224a-4339-9918-334436fbbb99
relation.isAuthorOfPublication.latestForDiscovery3ba90ba4-aac8-4892-a30f-25a10bc27298

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