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dc.contributor.authorPanneri, S.
dc.contributor.authorGanguly, P.
dc.contributor.authorNair, Balagopal
dc.contributor.authorMohamed, A.
dc.contributor.authorWarrier, K.
dc.contributor.authorHareesh, U.
dc.date.accessioned2017-03-15T22:24:10Z
dc.date.available2017-03-15T22:24:10Z
dc.date.created2017-03-08T06:39:37Z
dc.date.issued2017
dc.identifier.citationPanneri, S. and Ganguly, P. and Nair, B. and Mohamed, A. and Warrier, K. and Hareesh, U. 2017. Role of precursors on the photophysical properties of carbon nitride and its application for antibiotic degradation. Environmental Science and Pollution Research. 24 (9): pp. 8609-8618.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/50470
dc.identifier.doi10.1007/s11356-017-8538-z
dc.description.abstract

In this paper, we provide a comprehensive evaluation of graphitic carbon nitride (C3N4) powders derived from the four different precursors melamine, cyanamide, thiourea, and urea for the photocatalytic degradation of tetracycline (TC) antibiotic under sunlight irradiation. The powders were synthesized by employing the conventional thermal decomposition method. The synthesized powders were examined using different characterization tools for evaluating the photophysical properties. The degradation profile revealed that urea-derived C3N4 showed the highest activity while melamine-derived C3N4 showed the least activity. The TC degradation efficiency of the photocatalyst was found to be influenced more by the surface area values despite extended absorption by melamine in the visible light region. Stability tests on urea-derived C3N4 and others were checked by four runs of TC degradation under sunlight irradiation. The synthesized C3N4 powders also confirmed the dominance of urea-derived powders for cyclic stability.

dc.publisherSpringer
dc.titleRole of precursors on the photophysical properties of carbon nitride and its application for antibiotic degradation
dc.typeJournal Article
dcterms.source.startPage1
dcterms.source.endPage10
dcterms.source.issn0944-1344
dcterms.source.titleEnvironmental Science and Pollution Research
curtin.departmentNanochemistry Research Institute
curtin.accessStatusFulltext not available


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