Photocatalytic oxidation of methyl orange in presence of titanium dioxide in aqueous suspension. Part II: kinetics study [An article from: Desalination]
Book Details
Author(s)N. Guettai, H. Ait Amar
PublisherElsevier
ISBN / ASINB000RR5CZE
ISBN-13978B000RR5CZ7
AvailabilityAvailable for download now
Sales Rank99,999,999
MarketplaceUnited States 🇺🇸
Description
This digital document is a journal article from Desalination, published by Elsevier in . The article is delivered in HTML format and is available in your Amazon.com Media Library immediately after purchase. You can view it with any web browser.
Description:
The kinetics study of the adsorption and degradation phenomena involved in the photocatalytic degradation of Methyl Orange (MeO) were investigated using a batch reactor and artificial UV-light. Experiments were performed in a suspended TiO"2 (Degussa P-25) system at pH=3 and mass catalyst 0.8 g/L. The initial concentrations of MeO were varied in the range 5-75 ppm. From the results, the adsorption was found to be an essential factor in the photodegradability of the dye. The Linear transform of the Langmuir isotherm curve was further used to determine the characteristic parameters witch were: Q"m"a=14.65 mg g^-^1 and K"a"d=7.06x10^-^2 L mg^-^1. The kinetic analysis of the photodecomposition of MeO showed that the disappearance followed satisfactory the pseudo first-order according to Langmuir-Hinshelwood model. The adsorption constant calculated from the linear form of this model, K"a"d"s (7.79x10^-^2) was found quietly higher than K"a"d"s deducted from isotherm adsorption. At high initial concentrations of MeO, the low efficiency of the photocatalytic process may result from the inhibition of the by-products during the dye transformation. This inhibition was estimated by comparing to observed and estimated half-lives time.
Description:
The kinetics study of the adsorption and degradation phenomena involved in the photocatalytic degradation of Methyl Orange (MeO) were investigated using a batch reactor and artificial UV-light. Experiments were performed in a suspended TiO"2 (Degussa P-25) system at pH=3 and mass catalyst 0.8 g/L. The initial concentrations of MeO were varied in the range 5-75 ppm. From the results, the adsorption was found to be an essential factor in the photodegradability of the dye. The Linear transform of the Langmuir isotherm curve was further used to determine the characteristic parameters witch were: Q"m"a=14.65 mg g^-^1 and K"a"d=7.06x10^-^2 L mg^-^1. The kinetic analysis of the photodecomposition of MeO showed that the disappearance followed satisfactory the pseudo first-order according to Langmuir-Hinshelwood model. The adsorption constant calculated from the linear form of this model, K"a"d"s (7.79x10^-^2) was found quietly higher than K"a"d"s deducted from isotherm adsorption. At high initial concentrations of MeO, the low efficiency of the photocatalytic process may result from the inhibition of the by-products during the dye transformation. This inhibition was estimated by comparing to observed and estimated half-lives time.
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