Influence of the Interfacial pH on Electrochemical CaCO[sub 3] Precipitation

The influence of the pH at the electrode/solution interface on precipitation by means of electrochemistry was studied both theoretically and experimentally in pure calcocarbonic aqueous solutions. This interfacial pH was measured at the electrode by using a pH sensor-grid assembly in a submerged imp...

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Bibliographic Details
Published in:Journal of The Electrochemical Society
Main Authors: Tlili, M., Benamor, M., Gabrielli, Claude, Perrot, Hubert, Tribollet, Bernard
Other Authors: INRST, Université de Tunisie, Laboratoire Interfaces et Systèmes Electrochimiques (LISE), Institut de Chimie - CNRS Chimie (INC-CNRS)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)
Format: Article in Journal/Newspaper
Language:English
Published: HAL CCSD 2003
Subjects:
[CHIM]Chemical Sciences
Carbonic acid
Online Access:https://hal.sorbonne-universite.fr/hal-04219348
https://doi.org/10.1149/1.1613294
Description
Summary:The influence of the pH at the electrode/solution interface on precipitation by means of electrochemistry was studied both theoretically and experimentally in pure calcocarbonic aqueous solutions. This interfacial pH was measured at the electrode by using a pH sensor-grid assembly in a submerged impinging cell. A model which takes into account the electrochemical oxygen reduction and the chemical dissociation of hydrogen carbonate and carbonic acid is proposed to calculate the pH at the electrode/solution interface. It can reproduce the data using values of adjustable parameters obtained from experiments. Hence, the local concentrations of and the supersaturation coefficient, β, were determined at the electrode. These data were used to interpret precipitation on a gold electrode.

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