Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/4989
Full metadata record
DC FieldValueLanguage
dc.contributor.authorShahansha, M-
dc.contributor.authorSreelakshmi, P-
dc.contributor.authorDevika, D-
dc.contributor.authorRiona, R-
dc.contributor.authorSatyajit, S-
dc.date.accessioned2025-11-12T09:50:16Z-
dc.date.available2025-11-12T09:50:16Z-
dc.date.issued2025-06-15-
dc.identifier.citationChemical Engineering Science; 312:121649en_US
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0009250925004725-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/4989-
dc.description.abstractExisting regeneration techniques, utilized for silica (SiO2)-based organic dye adsorbents, are associated with several limitations. Hence, the regeneration of SiO2-Ag (10 wt%) nanocomposite, as a dye adsorbent, has been demonstrated here via the integration of surface plasmon resonance (SPR) of Ag0 and photocatalytic activity (PCA) of Ag2O with Fenton-like advanced oxidation process (AOP) under the visible light and solar irradiations to obtain the regeneration efficiency (RE) values of 65 % and 102 %. The addition of H2O2 and PS under the visible light irradiation is noted to increase the RE to 116 % and 123 %; while, that under the solar radiation, it is noted to increase the RE to 126 %. The regeneration of SiO2-Ag (10 wt%) nanocomposite obtained via the integration of weak SPR effect with Fenton-like AOP under the visible light irradiation is as effective as the integration of PCA with Fenton-like AOP under the solar irradiation.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.subjectRegenerationen_US
dc.subjectHydroxyl radicalen_US
dc.subjectSPR effecten_US
dc.subjectPhotocatalytic activityen_US
dc.subjectFenton-likeen_US
dc.subjectAdsorptionen_US
dc.titleIntegration of surface plasmon resonance and photocatalytic activity with Fenton-like advanced oxidation process for effective regeneration of SiO2-Ag nanocomposite in basic dye removal via adsorptionen_US
dc.typeArticleen_US
Appears in Collections:2025



Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.