Nonlinear Modelling of Kinetic Data Obtained from Photocatalytic Mineralisation of 2,4-Dichlorophenol on a Titanium Dioxide Membrane

Photomineralisation of 2,4-dichlorophenol (DCP) in aqueous solutions (10.0–100.0 mg/L of C) was systematically studied at 318±3 K, in an annular laboratory-scale reactor, by photocatalytic membranes immobilizing titanium dioxide, as a function of substrate concentration, and absorbed power per unit...

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Main Authors: Ignazio Renato Bellobono, Roberto Scotti, Massimiliano D'Arienzo, Franca Morazzoni, Riccardo Bianchi, Rodica Stanescu, Cristina Costache, Liliana Bobirica, Gabriela Cobzaru, Paola Maria Tozzi, Mauro Rossi, Mauro Luigi Bonardi, Flavia Groppi, Luigi Gini
Format: Article
Language:English
Published: Wiley 2009-01-01
Series:International Journal of Photoenergy
Online Access:http://dx.doi.org/10.1155/2009/631768
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author Ignazio Renato Bellobono
Roberto Scotti
Massimiliano D'Arienzo
Franca Morazzoni
Riccardo Bianchi
Rodica Stanescu
Cristina Costache
Liliana Bobirica
Gabriela Cobzaru
Paola Maria Tozzi
Mauro Rossi
Mauro Luigi Bonardi
Flavia Groppi
Luigi Gini
author_facet Ignazio Renato Bellobono
Roberto Scotti
Massimiliano D'Arienzo
Franca Morazzoni
Riccardo Bianchi
Rodica Stanescu
Cristina Costache
Liliana Bobirica
Gabriela Cobzaru
Paola Maria Tozzi
Mauro Rossi
Mauro Luigi Bonardi
Flavia Groppi
Luigi Gini
author_sort Ignazio Renato Bellobono
collection DOAJ
description Photomineralisation of 2,4-dichlorophenol (DCP) in aqueous solutions (10.0–100.0 mg/L of C) was systematically studied at 318±3 K, in an annular laboratory-scale reactor, by photocatalytic membranes immobilizing titanium dioxide, as a function of substrate concentration, and absorbed power per unit length of membrane. Kinetics of both substrate disappearance, to yield intermediates, and total organic carbon (TOC) disappearance, to yield carbon dioxide, were followed (first series of experiments). At a fixed value of irradiance (1.50 W⋅cm−1), other series of mineralization experiments were repeated (second series of experiments) by carrying out only analyses of chemical oxygen demand (COD), in order to compare modelling results of the two sets of experiments. In both sets of experiments, stoichiometric hydrogen peroxide was used as oxygen donor. For the first series of experiments, a kinetic model was employed, already validated in previous work, from which, by a set of differential equations, four final optimised parameters, k1 and K1, k2 and K2, were calculated. By these parameters, the whole kinetic profile could be fitted adequately. The influence of irradiance on k1 and k2 could be rationalised very well by this four-parameter kinetic model. Modelling of quantum yields, as a function of irradiance, could also be carried out satisfactorily. As has been found previously for other kinds of substrates, modelling of quantum yields for DCP mineralization is consistent with kinetics of hydroxyl radicals reacting between themselves, leading to hydrogen peroxide, other than with substrate or intermediates leading finally to carbon dioxide, paralleled by a second competition kinetics involving superoxide radical anion. For the second series of experiments, on the contrary, the Langmuir-Hinshelwood model was employed. Uncertainties of COD analyses, coupled with discrepancies of this model and with its inability to reproduce kinetics up to complete mineralization, are underlined.
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spelling doaj-art-6100b8a3ef8f4858b609b8aec05c7d912025-02-03T05:47:44ZengWileyInternational Journal of Photoenergy1110-662X1687-529X2009-01-01200910.1155/2009/631768631768Nonlinear Modelling of Kinetic Data Obtained from Photocatalytic Mineralisation of 2,4-Dichlorophenol on a Titanium Dioxide MembraneIgnazio Renato Bellobono0Roberto Scotti1Massimiliano D'Arienzo2Franca Morazzoni3Riccardo Bianchi4Rodica Stanescu5Cristina Costache6Liliana Bobirica7Gabriela Cobzaru8Paola Maria Tozzi9Mauro Rossi10Mauro Luigi Bonardi11Flavia Groppi12Luigi Gini13Environmental Research Centre, University of Milan, via C. Golgi 19, 20133 Milan, ItalyDepartment of Materials Science, University of Milano Bicocca, via R. Cozzi 53, 20126 Milan, ItalyDepartment of Materials Science, University of Milano Bicocca, via R. Cozzi 53, 20126 Milan, ItalyDepartment of Materials Science, University of Milano Bicocca, via R. Cozzi 53, 20126 Milan, ItalyISTM, Institute of Molecular Sciences and Technologies, CNR, 20133 Milan , ItalyDepartment of Inorganic Technology and Environmental Protection, Polytechnic University of Bucharest, 011061 Bucharest, RomaniaDepartment of Inorganic Technology and Environmental Protection, Polytechnic University of Bucharest, 011061 Bucharest, RomaniaDepartment of Inorganic Technology and Environmental Protection, Polytechnic University of Bucharest, 011061 Bucharest, RomaniaDepartment of Inorganic Technology and Environmental Protection, Polytechnic University of Bucharest, 011061 Bucharest, RomaniaR&D Group, BIT srl, 20121 Milan, ItalyLASA, Department of Physics, University of Milan, (National Institute of Nuclear Physics) INFN, 20133 Milan, ItalyLASA, Department of Physics, University of Milan, (National Institute of Nuclear Physics) INFN, 20133 Milan, ItalyLASA, Department of Physics, University of Milan, (National Institute of Nuclear Physics) INFN, 20133 Milan, ItalyLASA, Department of Physics, University of Milan, (National Institute of Nuclear Physics) INFN, 20133 Milan, ItalyPhotomineralisation of 2,4-dichlorophenol (DCP) in aqueous solutions (10.0–100.0 mg/L of C) was systematically studied at 318±3 K, in an annular laboratory-scale reactor, by photocatalytic membranes immobilizing titanium dioxide, as a function of substrate concentration, and absorbed power per unit length of membrane. Kinetics of both substrate disappearance, to yield intermediates, and total organic carbon (TOC) disappearance, to yield carbon dioxide, were followed (first series of experiments). At a fixed value of irradiance (1.50 W⋅cm−1), other series of mineralization experiments were repeated (second series of experiments) by carrying out only analyses of chemical oxygen demand (COD), in order to compare modelling results of the two sets of experiments. In both sets of experiments, stoichiometric hydrogen peroxide was used as oxygen donor. For the first series of experiments, a kinetic model was employed, already validated in previous work, from which, by a set of differential equations, four final optimised parameters, k1 and K1, k2 and K2, were calculated. By these parameters, the whole kinetic profile could be fitted adequately. The influence of irradiance on k1 and k2 could be rationalised very well by this four-parameter kinetic model. Modelling of quantum yields, as a function of irradiance, could also be carried out satisfactorily. As has been found previously for other kinds of substrates, modelling of quantum yields for DCP mineralization is consistent with kinetics of hydroxyl radicals reacting between themselves, leading to hydrogen peroxide, other than with substrate or intermediates leading finally to carbon dioxide, paralleled by a second competition kinetics involving superoxide radical anion. For the second series of experiments, on the contrary, the Langmuir-Hinshelwood model was employed. Uncertainties of COD analyses, coupled with discrepancies of this model and with its inability to reproduce kinetics up to complete mineralization, are underlined.http://dx.doi.org/10.1155/2009/631768
spellingShingle Ignazio Renato Bellobono
Roberto Scotti
Massimiliano D'Arienzo
Franca Morazzoni
Riccardo Bianchi
Rodica Stanescu
Cristina Costache
Liliana Bobirica
Gabriela Cobzaru
Paola Maria Tozzi
Mauro Rossi
Mauro Luigi Bonardi
Flavia Groppi
Luigi Gini
Nonlinear Modelling of Kinetic Data Obtained from Photocatalytic Mineralisation of 2,4-Dichlorophenol on a Titanium Dioxide Membrane
International Journal of Photoenergy
title Nonlinear Modelling of Kinetic Data Obtained from Photocatalytic Mineralisation of 2,4-Dichlorophenol on a Titanium Dioxide Membrane
title_full Nonlinear Modelling of Kinetic Data Obtained from Photocatalytic Mineralisation of 2,4-Dichlorophenol on a Titanium Dioxide Membrane
title_fullStr Nonlinear Modelling of Kinetic Data Obtained from Photocatalytic Mineralisation of 2,4-Dichlorophenol on a Titanium Dioxide Membrane
title_full_unstemmed Nonlinear Modelling of Kinetic Data Obtained from Photocatalytic Mineralisation of 2,4-Dichlorophenol on a Titanium Dioxide Membrane
title_short Nonlinear Modelling of Kinetic Data Obtained from Photocatalytic Mineralisation of 2,4-Dichlorophenol on a Titanium Dioxide Membrane
title_sort nonlinear modelling of kinetic data obtained from photocatalytic mineralisation of 2 4 dichlorophenol on a titanium dioxide membrane
url http://dx.doi.org/10.1155/2009/631768
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