Dissolution of nickel oxide in oxalic acid aqueous solutions

The dissolution of nickel oxide (bunsenite) in acid solutions containing oxalic acid has been studied at 70.0°C. The dependencies of the rate of dissolution on total oxalate concentration and on pH have been explained by assuming a mechanism involving the transfer of two different surface complexes,...

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Autores principales: Figueroa, C.A., Sileo, E.E., Morando, P.J., Blesa, M.A.
Formato: JOUR
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pH
Acceso en línea:http://hdl.handle.net/20.500.12110/paper_00219797_v244_n2_p353_Figueroa
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spelling todo:paper_00219797_v244_n2_p353_Figueroa2023-10-03T14:25:11Z Dissolution of nickel oxide in oxalic acid aqueous solutions Figueroa, C.A. Sileo, E.E. Morando, P.J. Blesa, M.A. Dissolution Nickel oxide Oxalic acid Surface complexation Carboxylic acids Complexation Dissolution Fourier transform infrared spectroscopy pH effects Solutions Stability constants Nickel compounds nickel oxalic acid aqueous solution article complex formation concentration (parameters) dissolution Fourier analysis infrared spectroscopy molecular stability pH priority journal synthesis temperature dependence transport kinetics The dissolution of nickel oxide (bunsenite) in acid solutions containing oxalic acid has been studied at 70.0°C. The dependencies of the rate of dissolution on total oxalate concentration and on pH have been explained by assuming a mechanism involving the transfer of two different surface complexes, I and II, that predominate in different pH ranges. The rate law is R = k1 {I} + k2 {II}, where {} denotes surface concentration. The values k1Ns = 3.04 × 10-3 mol Ni m-2 s-1, k2Ns = 1.84 × 10-3 mol Ni m-2 s-1, together with the stability constants K1 = 675 mol-1 dm3 and K2 = 60 mol-1 dm3 fit all the results very well. The species formed in more acidic media is both more stable and more reactive. The possible structures of I and II are discussed on the basis of Fourier transform IR spectroscopy evidence in the literature. © 2001 Elsevier Science. Fil:Sileo, E.E. 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_v244_n2_p353_Figueroa
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Dissolution
Nickel oxide
Oxalic acid
Surface complexation
Carboxylic acids
Complexation
Dissolution
Fourier transform infrared spectroscopy
pH effects
Solutions
Stability constants
Nickel compounds
nickel
oxalic acid
aqueous solution
article
complex formation
concentration (parameters)
dissolution
Fourier analysis
infrared spectroscopy
molecular stability
pH
priority journal
synthesis
temperature dependence
transport kinetics
spellingShingle Dissolution
Nickel oxide
Oxalic acid
Surface complexation
Carboxylic acids
Complexation
Dissolution
Fourier transform infrared spectroscopy
pH effects
Solutions
Stability constants
Nickel compounds
nickel
oxalic acid
aqueous solution
article
complex formation
concentration (parameters)
dissolution
Fourier analysis
infrared spectroscopy
molecular stability
pH
priority journal
synthesis
temperature dependence
transport kinetics
Figueroa, C.A.
Sileo, E.E.
Morando, P.J.
Blesa, M.A.
Dissolution of nickel oxide in oxalic acid aqueous solutions
topic_facet Dissolution
Nickel oxide
Oxalic acid
Surface complexation
Carboxylic acids
Complexation
Dissolution
Fourier transform infrared spectroscopy
pH effects
Solutions
Stability constants
Nickel compounds
nickel
oxalic acid
aqueous solution
article
complex formation
concentration (parameters)
dissolution
Fourier analysis
infrared spectroscopy
molecular stability
pH
priority journal
synthesis
temperature dependence
transport kinetics
description The dissolution of nickel oxide (bunsenite) in acid solutions containing oxalic acid has been studied at 70.0°C. The dependencies of the rate of dissolution on total oxalate concentration and on pH have been explained by assuming a mechanism involving the transfer of two different surface complexes, I and II, that predominate in different pH ranges. The rate law is R = k1 {I} + k2 {II}, where {} denotes surface concentration. The values k1Ns = 3.04 × 10-3 mol Ni m-2 s-1, k2Ns = 1.84 × 10-3 mol Ni m-2 s-1, together with the stability constants K1 = 675 mol-1 dm3 and K2 = 60 mol-1 dm3 fit all the results very well. The species formed in more acidic media is both more stable and more reactive. The possible structures of I and II are discussed on the basis of Fourier transform IR spectroscopy evidence in the literature. © 2001 Elsevier Science.
format JOUR
author Figueroa, C.A.
Sileo, E.E.
Morando, P.J.
Blesa, M.A.
author_facet Figueroa, C.A.
Sileo, E.E.
Morando, P.J.
Blesa, M.A.
author_sort Figueroa, C.A.
title Dissolution of nickel oxide in oxalic acid aqueous solutions
title_short Dissolution of nickel oxide in oxalic acid aqueous solutions
title_full Dissolution of nickel oxide in oxalic acid aqueous solutions
title_fullStr Dissolution of nickel oxide in oxalic acid aqueous solutions
title_full_unstemmed Dissolution of nickel oxide in oxalic acid aqueous solutions
title_sort dissolution of nickel oxide in oxalic acid aqueous solutions
url http://hdl.handle.net/20.500.12110/paper_00219797_v244_n2_p353_Figueroa
work_keys_str_mv AT figueroaca dissolutionofnickeloxideinoxalicacidaqueoussolutions
AT sileoee dissolutionofnickeloxideinoxalicacidaqueoussolutions
AT morandopj dissolutionofnickeloxideinoxalicacidaqueoussolutions
AT blesama dissolutionofnickeloxideinoxalicacidaqueoussolutions
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