Kinetics of adsorption of oxalic acid on different titanium dioxide samples

FTIR-ATR kinetic studies on the adsorption of oxalic acid on different TiO2 films were performed. The particulate films were obtained through the evaporation of TiO2 suspensions. The evolution of the IR bands followed a pseudo-first-order behavior, as previously observed. Systematic studies as a fun...

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Autores principales: Roncaroli, F., Blesa, M.A.
Formato: JOUR
Materias:
ATR
TiO
Acceso en línea:http://hdl.handle.net/20.500.12110/paper_00219797_v356_n1_p227_Roncaroli
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spelling todo:paper_00219797_v356_n1_p227_Roncaroli2023-10-03T14:25:13Z Kinetics of adsorption of oxalic acid on different titanium dioxide samples Roncaroli, F. Blesa, M.A. Adsorption ATR FTIR Kinetics Oxalic acid Surface complexation TiO2 Titanium dioxide ATR FTIR Oxalic Acid Surface complexation TiO Desorption Organic acids Oxides Rate constants Titanium Titanium dioxide Adsorption oxalic acid titanium dioxide adsorption kinetics article catalyst concentration (parameters) desorption diffusion evaporation evolution film infrared spectroscopy particle size particulate matter pollutant priority journal sensor suspension FTIR-ATR kinetic studies on the adsorption of oxalic acid on different TiO2 films were performed. The particulate films were obtained through the evaporation of TiO2 suspensions. The evolution of the IR bands followed a pseudo-first-order behavior, as previously observed. Systematic studies as a function of the oxalic acid concentration afforded the specific rate constant for adsorption (ka) and desorption (kd). The influence of physical parameters of the samples, i.e., specific BET area, crystalline domain size, TiO2 load, film area, and pore size, on the kinetic parameters ka and kd was analyzed. A mechanism in which the adsorption and desorption processes are controlled by the diffusion through the pores of the films is proposed (intraparticle diffusion). It is concluded that all the samples behave in the same way. Thicker films or those with smaller particle size (higher specific surface area, smaller pores) show the slowest rates of adsorption and desorption. These results are relevant for the design of efficient heterogeneous catalysts and sensors, and for the interpretation of pollutant adsorption. © 2010 Elsevier Inc. Fil:Roncaroli, F. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_00219797_v356_n1_p227_Roncaroli
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Adsorption
ATR
FTIR
Kinetics
Oxalic acid
Surface complexation
TiO2
Titanium dioxide
ATR
FTIR
Oxalic Acid
Surface complexation
TiO
Desorption
Organic acids
Oxides
Rate constants
Titanium
Titanium dioxide
Adsorption
oxalic acid
titanium dioxide
adsorption kinetics
article
catalyst
concentration (parameters)
desorption
diffusion
evaporation
evolution
film
infrared spectroscopy
particle size
particulate matter
pollutant
priority journal
sensor
suspension
spellingShingle Adsorption
ATR
FTIR
Kinetics
Oxalic acid
Surface complexation
TiO2
Titanium dioxide
ATR
FTIR
Oxalic Acid
Surface complexation
TiO
Desorption
Organic acids
Oxides
Rate constants
Titanium
Titanium dioxide
Adsorption
oxalic acid
titanium dioxide
adsorption kinetics
article
catalyst
concentration (parameters)
desorption
diffusion
evaporation
evolution
film
infrared spectroscopy
particle size
particulate matter
pollutant
priority journal
sensor
suspension
Roncaroli, F.
Blesa, M.A.
Kinetics of adsorption of oxalic acid on different titanium dioxide samples
topic_facet Adsorption
ATR
FTIR
Kinetics
Oxalic acid
Surface complexation
TiO2
Titanium dioxide
ATR
FTIR
Oxalic Acid
Surface complexation
TiO
Desorption
Organic acids
Oxides
Rate constants
Titanium
Titanium dioxide
Adsorption
oxalic acid
titanium dioxide
adsorption kinetics
article
catalyst
concentration (parameters)
desorption
diffusion
evaporation
evolution
film
infrared spectroscopy
particle size
particulate matter
pollutant
priority journal
sensor
suspension
description FTIR-ATR kinetic studies on the adsorption of oxalic acid on different TiO2 films were performed. The particulate films were obtained through the evaporation of TiO2 suspensions. The evolution of the IR bands followed a pseudo-first-order behavior, as previously observed. Systematic studies as a function of the oxalic acid concentration afforded the specific rate constant for adsorption (ka) and desorption (kd). The influence of physical parameters of the samples, i.e., specific BET area, crystalline domain size, TiO2 load, film area, and pore size, on the kinetic parameters ka and kd was analyzed. A mechanism in which the adsorption and desorption processes are controlled by the diffusion through the pores of the films is proposed (intraparticle diffusion). It is concluded that all the samples behave in the same way. Thicker films or those with smaller particle size (higher specific surface area, smaller pores) show the slowest rates of adsorption and desorption. These results are relevant for the design of efficient heterogeneous catalysts and sensors, and for the interpretation of pollutant adsorption. © 2010 Elsevier Inc.
format JOUR
author Roncaroli, F.
Blesa, M.A.
author_facet Roncaroli, F.
Blesa, M.A.
author_sort Roncaroli, F.
title Kinetics of adsorption of oxalic acid on different titanium dioxide samples
title_short Kinetics of adsorption of oxalic acid on different titanium dioxide samples
title_full Kinetics of adsorption of oxalic acid on different titanium dioxide samples
title_fullStr Kinetics of adsorption of oxalic acid on different titanium dioxide samples
title_full_unstemmed Kinetics of adsorption of oxalic acid on different titanium dioxide samples
title_sort kinetics of adsorption of oxalic acid on different titanium dioxide samples
url http://hdl.handle.net/20.500.12110/paper_00219797_v356_n1_p227_Roncaroli
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