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Kinetics and mechanism of deposition of zinc from zincate in concentrated alkali hydroxide solutions

Samo za registrovane korisnike
1976
Autori
Despić, Aleksandar R.
Jovanović, Đ.R.
Rakić, T.
Članak u časopisu (Objavljena verzija)
Metapodaci
Prikaz svih podataka o dokumentu
Apstrakt
Galvanostatic investigation has been carried out of the kinetics of the reaction on zinc amalgam hanging mercury drop immersed in alkaline zincate solutions at KOH concentrations ranging from 1 to 14 normal. Three kinds of data have been extracted: (i) the pseudo-capacitance as a function of overpotential from the portion of the charging curves prior to plateaux, (ii) the Tafel plots from quasi-steady state values at the plateaux and (iii) the Sand's products as function of current density from transition times. In (i), the pseudo-capacitance was found to increase with overpotential, in (ii), two slopes (60 mV dec-1 and 120 mV dec-1) have been found in the cathodic direction and a limiting current in the anodic one; in (iii), the Sand's product was found to decrease with increasing (i). On the basis of the above findings the reaction mechanism has been suggested to be of the cece type, with the chemical dissociation of the intermediate univalent zinc complex in between the two elctroch...emical steps as rate-determining. A modification of the method of evaluating the reaction orders was introduced to account for a simultaneous change of more than one activity of reactants in concentrated solutions. Using this, reaction order was found to be 2 with respect to both OH- ions and water, suggesting that the electroactive species is not only reduced in the number of ligands but also dehydrated with respect to the prevailing species. The anodic limiting current appears to be due to the accumulation of Zn(OH) species to cover all the surface free of adsorbed Zn(OH)2. Exchange cd and rate constants of all the four steps of the reaction have been estimated.

Ključne reči:
kinetics / zincate / zinc / Electrochemistry
Izvor:
Electrochimica Acta, 1976, 21, 1, 63-77
Izdavač:
  • Elsevier
Finansiranje / projekti:
  • The National Science Foundation (Washington, DC U.S.A.) within the PL-480 Programm

DOI: 10.1016/0013-4686(76)85111-0

ISSN: 0013-4686

Scopus: 2-s2.0-0039285657
[ Google Scholar ]
48
URI
https://cer.ihtm.bg.ac.rs/handle/123456789/4539
Kolekcije
  • Radovi istraživača / Researchers' publications
Institucija/grupa
IHTM
TY  - JOUR
AU  - Despić, Aleksandar R.
AU  - Jovanović, Đ.R.
AU  - Rakić, T.
PY  - 1976
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4539
AB  - Galvanostatic investigation has been carried out of the kinetics of the reaction on zinc amalgam hanging mercury drop immersed in alkaline zincate solutions at KOH concentrations ranging from 1 to 14 normal. Three kinds of data have been extracted: (i) the pseudo-capacitance as a function of overpotential from the portion of the charging curves prior to plateaux, (ii) the Tafel plots from quasi-steady state values at the plateaux and (iii) the Sand's products as function of current density from transition times. In (i), the pseudo-capacitance was found to increase with overpotential, in (ii), two slopes (60 mV dec-1 and 120 mV dec-1) have been found in the cathodic direction and a limiting current in the anodic one; in (iii), the Sand's product was found to decrease with increasing (i). On the basis of the above findings the reaction mechanism has been suggested to be of the cece type, with the chemical dissociation of the intermediate univalent zinc complex in between the two elctrochemical steps as rate-determining. A modification of the method of evaluating the reaction orders was introduced to account for a simultaneous change of more than one activity of reactants in concentrated solutions. Using this, reaction order was found to be 2 with respect to both OH- ions and water, suggesting that the electroactive species is not only reduced in the number of ligands but also dehydrated with respect to the prevailing species. The anodic limiting current appears to be due to the accumulation of Zn(OH) species to cover all the surface free of adsorbed Zn(OH)2. Exchange cd and rate constants of all the four steps of the reaction have been estimated.
PB  - Elsevier
T2  - Electrochimica Acta
T1  - Kinetics and mechanism of deposition of zinc from zincate in concentrated alkali hydroxide solutions
VL  - 21
IS  - 1
SP  - 63
EP  - 77
DO  - 10.1016/0013-4686(76)85111-0
ER  - 
@article{
author = "Despić, Aleksandar R. and Jovanović, Đ.R. and Rakić, T.",
year = "1976",
abstract = "Galvanostatic investigation has been carried out of the kinetics of the reaction on zinc amalgam hanging mercury drop immersed in alkaline zincate solutions at KOH concentrations ranging from 1 to 14 normal. Three kinds of data have been extracted: (i) the pseudo-capacitance as a function of overpotential from the portion of the charging curves prior to plateaux, (ii) the Tafel plots from quasi-steady state values at the plateaux and (iii) the Sand's products as function of current density from transition times. In (i), the pseudo-capacitance was found to increase with overpotential, in (ii), two slopes (60 mV dec-1 and 120 mV dec-1) have been found in the cathodic direction and a limiting current in the anodic one; in (iii), the Sand's product was found to decrease with increasing (i). On the basis of the above findings the reaction mechanism has been suggested to be of the cece type, with the chemical dissociation of the intermediate univalent zinc complex in between the two elctrochemical steps as rate-determining. A modification of the method of evaluating the reaction orders was introduced to account for a simultaneous change of more than one activity of reactants in concentrated solutions. Using this, reaction order was found to be 2 with respect to both OH- ions and water, suggesting that the electroactive species is not only reduced in the number of ligands but also dehydrated with respect to the prevailing species. The anodic limiting current appears to be due to the accumulation of Zn(OH) species to cover all the surface free of adsorbed Zn(OH)2. Exchange cd and rate constants of all the four steps of the reaction have been estimated.",
publisher = "Elsevier",
journal = "Electrochimica Acta",
title = "Kinetics and mechanism of deposition of zinc from zincate in concentrated alkali hydroxide solutions",
volume = "21",
number = "1",
pages = "63-77",
doi = "10.1016/0013-4686(76)85111-0"
}
Despić, A. R., Jovanović, Đ.R.,& Rakić, T.. (1976). Kinetics and mechanism of deposition of zinc from zincate in concentrated alkali hydroxide solutions. in Electrochimica Acta
Elsevier., 21(1), 63-77.
https://doi.org/10.1016/0013-4686(76)85111-0
Despić AR, Jovanović Đ, Rakić T. Kinetics and mechanism of deposition of zinc from zincate in concentrated alkali hydroxide solutions. in Electrochimica Acta. 1976;21(1):63-77.
doi:10.1016/0013-4686(76)85111-0 .
Despić, Aleksandar R., Jovanović, Đ.R., Rakić, T., "Kinetics and mechanism of deposition of zinc from zincate in concentrated alkali hydroxide solutions" in Electrochimica Acta, 21, no. 1 (1976):63-77,
https://doi.org/10.1016/0013-4686(76)85111-0 . .

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