Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.11861/6525
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dc.contributor.authorMoosavi, Seyedehmaryamen_US
dc.contributor.authorDr. LI Yi Man, Ritaen_US
dc.contributor.authorLai, Chin Weien_US
dc.contributor.authorYusof, Yuslizaen_US
dc.contributor.authorGan, Sinyeeen_US
dc.contributor.authorAkbarzadeh, Omiden_US
dc.contributor.authorChowhury, Zaira Zamanen_US
dc.contributor.authorYue, Xiao-Guangen_US
dc.contributor.authorJohan, Mohd RafieBinen_US
dc.date.accessioned2021-03-07T08:33:47Z-
dc.date.available2021-03-07T08:33:47Z-
dc.date.issued2020-
dc.identifier.citationNanomaterials, 2020, vol. 10(12), article no. 2360.en_US
dc.identifier.issn2079-4991-
dc.identifier.urihttp://hdl.handle.net/20.500.11861/6525-
dc.description.abstractIn this study, activated carbon (AC) from coconut shell, as a widely available agricultural waste, was synthesised in a simple one-step procedure and used to produce a magnetic Fe3O4/AC/TiO2 nano-catalyst for the degradation of methylene blue (MB) dye under UV light. Scanning electron microscopy revealed that TiO2 nanoparticles, with an average particle size of 45 to 62 nm, covered the surface of the AC porous structure without a reunion of its structure, which according to the TGA results enhanced the stability of the photocatalyst at high temperatures. The photocatalytic activities of synthesised AC, commercial TiO2, Fe3O4/AC, and Fe3O4/AC/TiO2 were compared, with Fe3O4/AC/TiO2 (1:2) exhibiting the highest catalytic activity (98%). Furthermore, evaluation of the recovery and reusability of the photocatalysts after treatment revealed that seven treatment cycles were possible without a significant reduction in the removal efficiency.en_US
dc.language.isoenen_US
dc.relation.ispartofNanomaterialsen_US
dc.titleMethylene blue dye photocatalytic degradation over synthesised Fe3O4/AC/TiO2 nano-catalyst: Degradation and reusability studiesen_US
dc.typePeer Reviewed Journal Articleen_US
dc.identifier.doi10.3390/nano10122360-
item.fulltextNo Fulltext-
crisitem.author.deptDepartment of Economics and Finance-
Appears in Collections:Economics and Finance - Publication
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