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dc.contributor.authorMd Rosli Noor Izzati;Lam Sze-Mun;Sin Jin-Chung;Satoshi Ichikawa;Mohamed Abdul Rahman
dc.date.accessioned2019-02-26T07:56:20Z
dc.date.available2019-02-26T07:56:20Z
dc.date.issued2018
dc.identifier.other%28ASCE%29EE.1943-7870.0001300.pdf
dc.identifier.urihttp://yetl.yabesh.ir/yetl1/handle/yetl/4250400
dc.description.abstractA ZnO/g-C3N4 photocatalyst was successfully synthesized via an impregnation method. The high-resolution transmission electron microscope (HRTEM) result shows that g-C3N4 had coated the surface of ZnO, indicating a sufficient blending between ZnO and g-C3N4 during synthesis. Reduced photoluminescence (PL) intensity of the ZnO/g-C3N4 reveals the synergic effect of the hybrid nanoparticles on the recombination of photoinduced electron–hole pairs. The resultant ZnO/g-C3N4 photocatalysts show higher degradation efficiency of phenol than that of pure ZnO under simulated sunlight irradiation. Especially, the ZnO/(5  wt%) g-C3N4 demonstrate the highest photodegradation efficiency of phenol because of the high amount of •OH radicals generated in the photocatalytic reaction. Process parameters such as photocatalyst amount, initial phenol concentration, and solution pH show a remarkable effect on the photocatalytic activity of ZnO/g-C3N4. The degradation mechanism of phenol is also detailed through identification of product intermediates and detection of reactive species. Moreover, the ZnO/g-C3N4 photocatalyst could be reused several times without appreciable loss of activity, showing great potential to be an excellent candidate for environmental remediation.
dc.publisherAmerican Society of Civil Engineers
dc.titlePhotocatalytic Performance of ZnO/g-C3N4 for Removal of Phenol under Simulated Sunlight Irradiation
dc.typeJournal Paper
dc.journal.volume144
dc.journal.issue2
dc.journal.titleJournal of Environmental Engineering
dc.identifier.doi10.1061/(ASCE)EE.1943-7870.0001300
dc.page4017091
dc.treeJournal of Environmental Engineering:;2018:;Volume ( 144 ):;issue: 002
dc.contenttypeFulltext


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