Factors influencing the photocatalytic decolorization of Bromophenol blue in aqueous solution with different types of TiO2 as photocatalysts

• Published in: Desalination Vol. 275; no. 1-3; pp. 224 - 230
• Main Authors: BOUANIMBA, Nour, ZOUAGHI, Razika, LAID, Nassima, SEHILI, Tahar
• Format: Journal Article
• Language: English
• Published: Amsterdam Elsevier 15.07.2011
• Subjects: Adsorption; Applied sciences; Bromophenol blue; Catalysis; Catalytic reactions; Chemical engineering; Chemistry; Decoloring; Degradation; Exact sciences and technology; General and physical chemistry; Mathematical models; Photocatalysis; Photocatalysts; Pollution; Reactors; Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry; Titanium dioxide; Discoloration; Dyes; Hydrogen peroxide; Photocatalysis; Modeling; Operating conditions; Dye; Ultraviolet radiation; Decolorization; Adsorption; Loading; First order; pH; Kinetics; Aqueous solution; Bromophenol blue; Rate constant; Titanium oxide; Photocatalysts; Catalyst; Photochemical degradation
• ISSN: 0011-9164; 1873-4464
• DOI: 10.1016/j.desal.2011.03.005

The photocatalytic decolorization of Bromophenol blue (BPB) in aqueous solution with different types of TiO2 as photocatalysts in slurry form has been carried out using UV-A light at 365nm under a variety of conditions. The efficiency of P25-Degussa and PC500-Millennium photocatalysts were compared. The effects of various parameters such as catalyst loading, light intensity, temperature, pH and initial concentration of the dye on decolorization have been investigated. The adsorption of BPB on TiO2-P25 and PC500 was found favorable by the Langmuir approach. Under the operating conditions of this study, the photocatalytic degradation of BPB followed pseudo first-order decay kinetics. The kapp values indicated an inverse dependence on the initial dye concentration and were fitted to the Langmuir-Hinshelwood model. The degradation efficiency was found to increase with the pH at neutral to acidic ranges, however the reaction was gradually retarded at the alkaline medium due to the effect of charge repulsion. The degradation rate constants increase slightly with an increase in temperature from 10 to 50 degree C. The kinetics was strongly enhanced in the presence of electron acceptors such as H2O2 at low dosage.