Please use this identifier to cite or link to this item: http://hdl.handle.net/10773/37788
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dc.contributor.authorMatos, Renatapt_PT
dc.contributor.authorKuźniarska-Biernacka, Iwonapt_PT
dc.contributor.authorRocha, Marianapt_PT
dc.contributor.authorBelo, João H.pt_PT
dc.contributor.authorAraújo, João Pedropt_PT
dc.contributor.authorEstrada, Ana C.pt_PT
dc.contributor.authorLopes, Joana L.pt_PT
dc.contributor.authorShah, Tushtipt_PT
dc.contributor.authorKorgel, Brian A.pt_PT
dc.contributor.authorPereira, Clarapt_PT
dc.contributor.authorTrindade, Titopt_PT
dc.contributor.authorFreire, Cristinapt_PT
dc.date.accessioned2023-05-19T09:54:57Z-
dc.date.available2023-05-19T09:54:57Z-
dc.date.issued2023-06-01-
dc.identifier.issn0920-5861pt_PT
dc.identifier.urihttp://hdl.handle.net/10773/37788-
dc.description.abstractThis study describes nanocomposites of graphene flakes (GF) combined with CuS, Fe3O4 and CuS−Fe3O4 nanoparticles prepared by wet chemical methods. The Fe3O4 and/or CuS nanoparticles were directly anchored onto GF without requiring additional chemical treatment. The composition, structure and morphology of the nanocomposites, as well as of the pristine GF and metal oxide/sulfide nanoparticles were characterised by X − ray photoelectron spectroscopy (XPS), Raman spectroscopy, Fourier transform infrared spectroscopy (FTIR), powder X − ray diffraction (XRD) and scanning electron microscopy (SEM) techniques. The results confirmed the successful attachment of CuS nanophases (size range: 23.7–50.1 nm) and/or Fe3O4 nanoparticles (size range: 10.6–15.8 nm). The adsorption and photocatalytic properties of the GF−based nanocomposites were evaluated at room temperature using Rhodamine B (RhB) as a model contaminant. Theoretical models were fitted to the adsorption kinetic results using the pseudo-first-order, pseudo-second-order and Elovich equations, while the adsorption mechanism was determined using the intraparticle diffusion, Bangham and Boyd models. The RhB adsorption efficiency was 6.5% for GF@CuS−Fe3O4 after 180 min contact time, whereas for the other materials was significantly higher: 97.6%, 60.9% and 31.9% for GF, GF@CuS and GF@Fe3O4, respectively. The adsorption capacity of GF and composites fitted the pseudo−second−order kinetic and Elovich models. The influence of the nanostructures composition on the corresponding photocatalytic activity in the degradation of RhB under a 150 W halogen lamp was also evaluated. The GF@CuS−Fe3O4 nanocomposite totally eliminated the dissolved RhB after 60 min irradiation, whereas the GF@CuS, GF@Fe3O4 and pristine Fe3O4 removed 75.6%, 80.9% and 30.8%, respectively, after 180 min irradiation. It was found that the photocatalytic behaviour of the composites was best described by the first−order kinetic model. The rate constant of the photocatalytic RhB removal for GF@CuS−Fe3O4 (k = 7.05 ×10−2 min−1) was 2.1, 5.1 and 15.0 times higher than those obtained for GF@CuS, GF@Fe3O4 and pristine Fe3O4, respectively, after 60 min of visible light irradiation.pt_PT
dc.language.isoengpt_PT
dc.publisherElsevierpt_PT
dc.relationH2020-FETOPEN-2018-2019-2020-01pt_PT
dc.relation2021.04120. CEECIND/CP1662/CT0008pt_PT
dc.relationF-1464pt_PT
dc.relationDMR-1720595pt_PT
dc.relationinfo:eu-repo/grantAgreement/FCT/3599-PPCDT/PTDC%2FEME-TED%2F3099%2F2020/PTpt_PT
dc.relationCERN/FISTEC/0003/2019pt_PT
dc.relationinfo:eu-repo/grantAgreement/FCT/DL 57%2F2016/DL57%2F2016%2FCP1334%2FCP1644%2FCT0001/PTpt_PT
dc.relationSFRH-BPD-87430/2012pt_PT
dc.relationREQUIMTE/EEC2018/14pt_PT
dc.relationinfo:eu-repo/grantAgreement/FCT/POR_CENTRO/SFRH%2FBD%2F126241%2F2016/PTpt_PT
dc.rightsopenAccesspt_PT
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjectGraphene flakespt_PT
dc.subjectGraphene hybrid nanostructurespt_PT
dc.subjectIron oxide nanoparticlespt_PT
dc.subjectCopper sulfide nanocrystalspt_PT
dc.subjectRhodamine Bpt_PT
dc.subjectPhotocatalysispt_PT
dc.subjectAdsorptionpt_PT
dc.titleDesign and photo-Fenton performance of Graphene/CuS/Fe3O4 tertiary nanocomposites for Rhodamine B degradationpt_PT
dc.typearticlept_PT
dc.description.versionpublishedpt_PT
dc.peerreviewedyespt_PT
degois.publication.titleCatalysis Todaypt_PT
degois.publication.volume418pt_PT
dc.identifier.doi10.1016/j.cattod.2023.114132pt_PT
dc.identifier.essn1873-4308pt_PT
dc.identifier.articlenumber114132pt_PT
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