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Photodegradation of chloramphenicol and paracetamol using PbS/TiO2 nanocomposites produced by green synthesis

dc.contributor.authorPalma, Tânia Cristina da Luz
dc.contributor.authorVieira, Bernardete
dc.contributor.authorNunes, J.
dc.contributor.authorLourenço, J. P.
dc.contributor.authorMonteiro, O. C.
dc.contributor.authorCosta, Maria Clara
dc.date.accessioned2020-09-11T08:57:53Z
dc.date.available2020-09-11T08:57:53Z
dc.date.issued2020
dc.description.abstractThe present study describes the photocatalytic potential of the successfully synthesized nanocrystalline PbS/TiO2 nanocomposites in the photodegradation of chloramphenicol and paracetamol. PbS and PbS/TiO2 nanoparticles were synthesized using biological sulphide produced by sulphate-reducing bacteria in batch and in a coupled bioremediation system (upflow anaerobic packed-bed reactor) for acid mine drainage treatment, yielding near-complete metal precipitation (~ 100–99%, respectively). The PbS and PbS/TiO2 composites obtained using sulphide generated in batch have an average particle size ranging from 17 to 25 nm and 15 to 20 nm, respectively, while in bioreactor, both PbS and PbS/TiO2 particles have a similar size range from 20 to 50 nm. All the produced particles presented crystalline cubic structure. The specific surface area of TiO2 and PbS/TiO2 was estimated to be 46.559 m2/g and 38.005 m2/g, respectively. Chloramphenicol removal by photolysis was about 61% after 60 min of Hg irradiation and 36% under sunlight exposition. Chloramphenicol photodegradation using PbS/TiO2 as catalyst was successfully performed in a photoreactor (Hg medium pressure, 450 W) and under solar exposition with a high drug removal efficiency of 96% and 93% after 60 min and 240 min irradiation, respectively. Using TiO2 as a catalyst for photodegradation achieved 98% removal for both Hg and sunlight irradiation (UV index ranging 7–8) after 60 min and 240 min, respectively. Paracetamol removal by photolysis was about 18%. Drug’s photocatalytic degradation using PbS/TiO2 was successfully performed under sunlight exposition with a high removal efficiency of 93%, while in the presence of TiO2, the removal was complete, after 235 min irradiation.pt_PT
dc.description.sponsorshipUIDB/04326/2020, UID/QUI/00100/2019pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.doi10.1007/s13738-020-01906-1pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.1/14712
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherSpringerpt_PT
dc.relationBiodegradation of widely used pharmaceutical compounds by bacterial communities
dc.relation.publisherversionhttps://link.springer.com/article/10.1007/s13738-020-01906-1pt_PT
dc.subjectGreen synthesispt_PT
dc.subjectPbS nanoparticlespt_PT
dc.subjectPbS/TiO2 nanocompositespt_PT
dc.subjectPollutants photodegradationpt_PT
dc.titlePhotodegradation of chloramphenicol and paracetamol using PbS/TiO2 nanocomposites produced by green synthesispt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.awardTitleBiodegradation of widely used pharmaceutical compounds by bacterial communities
oaire.awardURIinfo:eu-repo/grantAgreement/FCT//SFRH%2FBD%2F95075%2F2013/PT
oaire.citation.endPage2031pt_PT
oaire.citation.issue8pt_PT
oaire.citation.startPage2013pt_PT
oaire.citation.titleJournal of the Iranian Chemical Societypt_PT
oaire.citation.volume17pt_PT
person.familyNameDa Luz Palma
person.familyNameVieira
person.familyNameLourenço
person.familyNameCosta
person.givenNameTânia Cristina
person.givenNameBernardete
person.givenNameJoão P.
person.givenNameMaria Clara
person.identifier634248
person.identifier.ciencia-id0614-DE1E-9632
person.identifier.ciencia-idF81F-A1F0-2A7C
person.identifier.ciencia-id7110-A28E-3C8A
person.identifier.orcid0000-0001-8614-570X
person.identifier.orcid0000-0002-6284-006X
person.identifier.orcid0000-0002-0501-6672
person.identifier.orcid0000-0003-1340-5237
person.identifier.ridA-7758-2008
person.identifier.ridM-6189-2013
person.identifier.scopus-author-id57195730600
person.identifier.scopus-author-id35354952400
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.nameFundação para a Ciência e a Tecnologia
rcaap.rightsrestrictedAccesspt_PT
rcaap.typearticlept_PT
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