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dc.contributor.authorBoz, Ismail
dc.contributor.authorKerkez, Ozge
dc.date.accessioned2021-03-04T13:27:12Z
dc.date.available2021-03-04T13:27:12Z
dc.date.issued2013
dc.identifier.citationKerkez O., Boz I., "Efficient removal of methylene blue by photocatalytic degradation with TiO2 nanorod array thin films", REACTION KINETICS MECHANISMS AND CATALYSIS, cilt.110, sa.2, ss.543-557, 2013
dc.identifier.issn1878-5190
dc.identifier.othervv_1032021
dc.identifier.otherav_7c7f9601-efae-4817-9ac4-c4084a49ae39
dc.identifier.urihttp://hdl.handle.net/20.500.12627/85140
dc.identifier.urihttps://doi.org/10.1007/s11144-013-0616-8
dc.description.abstractTiO2 nanorod array thin films were synthesized on fluorine doped tin oxide (FTO) glass substrate by the hydrothermal method. The prepared TiO2 nanorod arrays were characterized by X-ray diffraction, scanning electron microscopy and UV-Vis diffuse reflectance spectroscopy. The effect of different synthesis conditions was investigated on the growth and photocatalytic activity of the samples. X-ray diffraction results show that the main phase of TiO2 is rutile and nanorod growth significantly depends on the synthesis conditions. TiO2 nanorod array thin films were used for the photocatalytic degradation of methylene blue in aqueous solution under UV irradiation (254 and 365 nm). The hydrothermal synthesis conditions of TiO2/FTO sample were determined for maximum photodegradation efficiency. Total degradation of 94 % was achieved under 254 nm and 69 % degradation was achieved under 365 nm with TiO2/FTO sample prepared with initial HCl:H2O = 1:1 ratio, 1.0 ml TiCl4 at 180 A degrees C for 2 h hydrothermal growth. The apparent reaction rate constant was calculated to be 0.0108 min(-1) under 254 nm and 0.0044 min(-1) under 365 nm.
dc.language.isoeng
dc.subjectTemel Bilimler
dc.subjectFizikokimya
dc.subjectTemel Bilimler (SCI)
dc.subjectKimya
dc.subjectKİMYA, FİZİKSEL
dc.titleEfficient removal of methylene blue by photocatalytic degradation with TiO2 nanorod array thin films
dc.typeMakale
dc.relation.journalREACTION KINETICS MECHANISMS AND CATALYSIS
dc.contributor.departmentBeykent Üniversitesi , ,
dc.identifier.volume110
dc.identifier.issue2
dc.identifier.startpage543
dc.identifier.endpage557
dc.contributor.firstauthorID53239


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