Effect of a Fast Potential Change on the Early Stage of Zinc Passivation in a Saturated Calcium Hydroxide Solution

The fast and sharp corrosion potential change from the active state to the passive state, that pure zinc plates immersed in calcium hydroxide saturated solutions with and without chlorides spontaneously exhibit at the early stage of passivation, was studied. The corrosion behavior was investigated b...

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Main Authors: Armando Garnica-Rodríguez, R. Montoya, Francisco Javier Rodríguez-Gomez, Tezozomoc Pérez-López, Juan Genesca
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-06-01
Series:Frontiers in Materials
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fmats.2022.877728/full
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author Armando Garnica-Rodríguez
R. Montoya
Francisco Javier Rodríguez-Gomez
Tezozomoc Pérez-López
Juan Genesca
author_facet Armando Garnica-Rodríguez
R. Montoya
Francisco Javier Rodríguez-Gomez
Tezozomoc Pérez-López
Juan Genesca
author_sort Armando Garnica-Rodríguez
collection DOAJ
description The fast and sharp corrosion potential change from the active state to the passive state, that pure zinc plates immersed in calcium hydroxide saturated solutions with and without chlorides spontaneously exhibit at the early stage of passivation, was studied. The corrosion behavior was investigated by corrosion potential monitoring, anodic polarization curves and electrochemical impedance spectroscopy. The zinc surface was characterized by scanning electron microscopy and X-ray energy dispersive spectroscopy. Experimental results show that the presence of chlorides increases the rate of change of potential by 10-fold in the early stage of passivation, producing a porous passivating film of corrosion products mainly made of calcium hydroxy-zincate Ca(Zn(OH)3)2· 2 H2O, with a less protective barrier effect than the non-porous film formed without chlorides. On the other hand, a modeling approach was achieved by solving the transient 2D Nernst–Planck equations and considering 12 chemical species. Numerical results confirm that the composition of the chemical products generated on the Zn surface certainly depends on the concentration of Cl¯ ions: Simonkolleite and hidroxides become unstable in the presence of high Cl¯ concentrations, whereas calcium hydroxyl-zincate is the main chemical compound generated on the Zn surface. However, the presence of the latter compound is much more important in electrolytes with very low concentration of Cl¯ ions.
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spelling doaj.art-1384fe09b0d94ae9b1d820ea459ed24d2022-12-22T03:32:41ZengFrontiers Media S.A.Frontiers in Materials2296-80162022-06-01910.3389/fmats.2022.877728877728Effect of a Fast Potential Change on the Early Stage of Zinc Passivation in a Saturated Calcium Hydroxide SolutionArmando Garnica-Rodríguez0R. Montoya1Francisco Javier Rodríguez-Gomez2Tezozomoc Pérez-López3Juan Genesca4Departamento de Ingeniería Metalúrgica, Facultad de Química, Universidad Nacional Autónoma de México, México City, MexicoPolo Universitario de Tecnología Avanzada, PUNTA, Facultad Química, UNAM, Apodaca, MexicoDepartamento de Ingeniería Metalúrgica, Facultad de Química, Universidad Nacional Autónoma de México, México City, MexicoCentro de Investigación en Corrosión, Universidad Autónoma de Campeche, Campeche, MexicoPolo Universitario de Tecnología Avanzada, PUNTA, Facultad Química, UNAM, Apodaca, MexicoThe fast and sharp corrosion potential change from the active state to the passive state, that pure zinc plates immersed in calcium hydroxide saturated solutions with and without chlorides spontaneously exhibit at the early stage of passivation, was studied. The corrosion behavior was investigated by corrosion potential monitoring, anodic polarization curves and electrochemical impedance spectroscopy. The zinc surface was characterized by scanning electron microscopy and X-ray energy dispersive spectroscopy. Experimental results show that the presence of chlorides increases the rate of change of potential by 10-fold in the early stage of passivation, producing a porous passivating film of corrosion products mainly made of calcium hydroxy-zincate Ca(Zn(OH)3)2· 2 H2O, with a less protective barrier effect than the non-porous film formed without chlorides. On the other hand, a modeling approach was achieved by solving the transient 2D Nernst–Planck equations and considering 12 chemical species. Numerical results confirm that the composition of the chemical products generated on the Zn surface certainly depends on the concentration of Cl¯ ions: Simonkolleite and hidroxides become unstable in the presence of high Cl¯ concentrations, whereas calcium hydroxyl-zincate is the main chemical compound generated on the Zn surface. However, the presence of the latter compound is much more important in electrolytes with very low concentration of Cl¯ ions.https://www.frontiersin.org/articles/10.3389/fmats.2022.877728/fullEISgalvanizedconcretezinc passivationfast potential changemodeling
spellingShingle Armando Garnica-Rodríguez
R. Montoya
Francisco Javier Rodríguez-Gomez
Tezozomoc Pérez-López
Juan Genesca
Effect of a Fast Potential Change on the Early Stage of Zinc Passivation in a Saturated Calcium Hydroxide Solution
Frontiers in Materials
EIS
galvanized
concrete
zinc passivation
fast potential change
modeling
title Effect of a Fast Potential Change on the Early Stage of Zinc Passivation in a Saturated Calcium Hydroxide Solution
title_full Effect of a Fast Potential Change on the Early Stage of Zinc Passivation in a Saturated Calcium Hydroxide Solution
title_fullStr Effect of a Fast Potential Change on the Early Stage of Zinc Passivation in a Saturated Calcium Hydroxide Solution
title_full_unstemmed Effect of a Fast Potential Change on the Early Stage of Zinc Passivation in a Saturated Calcium Hydroxide Solution
title_short Effect of a Fast Potential Change on the Early Stage of Zinc Passivation in a Saturated Calcium Hydroxide Solution
title_sort effect of a fast potential change on the early stage of zinc passivation in a saturated calcium hydroxide solution
topic EIS
galvanized
concrete
zinc passivation
fast potential change
modeling
url https://www.frontiersin.org/articles/10.3389/fmats.2022.877728/full
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