Photocatalytic Degradation of Anthracene in Closed System Reactor

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dc.identifier.uri Karam, Faiq F. Hussein, Falah H. Baqir, Sadiq J. Halbus, Ahmed F. Dillert, Ralf Bahnemann, Detlef W. 2016-09-29T11:45:02Z 2016-09-29T11:45:02Z 2014
dc.identifier.citation Karam, Faiq F.; Hussein, Falah H.; Baqir, Sadiq J.; Halbus, Ahmed F.; Dillert, Ralf; Bahnemann, Detlef W.: Photocatalytic Degradation of Anthracene in Closed System Reactor. In: International Journal of Photoenergy 2014 (2014), 503825. DOI:
dc.description.abstract Polycyclic aromatic hydrocarbons (PAHs) represent a large class of persistent organic pollutants in an environment of special concern because they have carcinogenic and mutagenic activity. In this paper, we focus on and discuss the effect of different parameters, for instance, initial concentration of Anthracene, temperature, and light intensity, on the degradation rate. These parameters were adjusted at pH 6.8 in the presence of the semiconductor materials (TiO2) as photocatalysts overUVlight. The main product of Anthracene photodegradation is 9,10-Anthraquinone which isidentified and compared with the standard compound by GC-MS. Our results indicate that the optimum conditions for the best rate of degradation are 25 ppm concentration of Anthracene, regulating the reaction vessel at 308.15 K and 2.5 mW/cm(2) of light intensity at 17 5mg/100 mL of titanium dioxide (P25). eng
dc.language.iso eng
dc.publisher New York : Hindawi Publishing Corporation
dc.relation.ispartofseries International Journal of Photoenergy 2014 (2014)
dc.rights CC BY 3.0 Unported
dc.subject polycyclic aromatic-hydrocarbons eng
dc.subject dyeing waste-water eng
dc.subject titanium-dioxide eng
dc.subject soil surfaces eng
dc.subject uv-light eng
dc.subject fluorescence detection eng
dc.subject tio2 eng
dc.subject irradiation eng
dc.subject extraction eng
dc.subject pahs eng
dc.subject.ddc 500 | Naturwissenschaften ger
dc.subject.ddc 540 | Chemie ger
dc.title Photocatalytic Degradation of Anthracene in Closed System Reactor
dc.type article
dc.type Text
dc.relation.essn 1687-529X
dc.relation.issn 1110-662X
dc.bibliographicCitation.volume 2014
dc.bibliographicCitation.firstPage 503825
dc.description.version publishedVersion
tib.accessRights frei zug�nglich

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