CERES > School of Applied Sciences (SAS) (2006-July 2014) > Staff publications - School of Applied Sciences >

Please use this identifier to cite or link to this item: http://dspace.lib.cranfield.ac.uk/handle/1826/4115

Document Type: Article
Title: Kinetic study of adsorption and photo-decolorization of Reactive Red 198 on TiO2 surface
Authors: Dutta, S.
Parsons, Simon A.
Bhattacharjee, C.
Jarvis, Peter
Datta, S.
Bandyopadhyay, S.
Issue Date: 15-Dec-2009
Citation: S. Dutta, S.A. Parsons, C. Bhattacharjee, P. Jarvis, S. Datta, S. Bandyopadhyay, Kinetic study of adsorption and photo-decolorization of Reactive Red 198 on TiO2 surface, Chemical Engineering Journal, Volume 155, Issue 3, 15 December 2009, Pages 674-679
Abstract: Recycling and reuse of wastewater after purification will reduce the environmental pollution as well as fulfill the increasing demand of water. Adsorption-based water treatment process is very popular for dye-house wastewater treatment. The present study deals with treatment of wastewater contaminated by reactive dye. TiO2 is used as adsorbent and the spent adsorbent has been regenerated by Advanced Oxidation Process (AOP), without using any other chemicals. TiO2 adsorbs dye molecules and then those dye molecules have been oxidized via a photocatalytic reaction in presence of UV irradiation. Kinetics of dye adsorption and photocatalytic oxidation reaction has been developed in this study. Photocatalyst adsorbent (TiO2) has been reused several times after regeneration. The activity of catalyst decreases after each cycle; due to poisoning cause by intermediate by-products. Kinetic of this catalyst deactivation has been incorporated with L–H model to develop the photocatalytic reaction kinetic model.
URI: http://dx.doi.org/10.1016/j.cej.2009.08.026
Appears in Collections:Staff publications - School of Applied Sciences

Files in This Item:

File Description SizeFormat
Kinetic_study_of_adsorption_and_photo-decolorization-2009.pdf387.97 kBAdobe PDFView/Open

SFX Query

Items in CERES are protected by copyright, with all rights reserved, unless otherwise indicated.