A comparative study of silver electrodeposition from pyrophosphate-cyanide and high concentration cyanide electrolytes in the presence of brighteners

Hatice Kübra Akben*, Servet Ibrahim Timur

*Bu çalışma için yazışmadan sorumlu yazar

Araştırma sonucu: Dergiye katkıMakalebilirkişi

7 Atıf (Scopus)

Özet

A study of the electrodeposition of silver from 2 different types of electrolytes; (1) neutral pyrophosphate-cyanide electrolyte and (2) alkaline high concentrated cyanide electrolyte in the presence of a variety of additives such as 2-mercaptobenzothiazole, potassium selenocyanate, and potassium antimony tartrate was performed. Influence of additives and cyanide concentration on microstructure and kinetics of the cathodic processes were studied. A brightener couple, 2-mercaptobenzothiazole and potassium antimony tartrate, were combined within this investigation and detected to be highly effective for silver electrodeposition. The rapid increase in current density at the same potential interval related to grain refinement effect of potassium antimony tartrate was shown. The cyclic organic compound, 2-mercaptobenzothiazole, polarizes the reduction to high cathodic potential in pyrophosphate electrolyte. However, the sufficient levelling effect required for the mirror-bright appearance seems to be related to the high polarizing effect of the high concentration cyanide content. In the case of pyrophosphate electrolytes, sufficient levelling cannot be achieved, so semigloss coatings are obtained. The low cathodic potential electrodeposition of silver in pyrophosphate electrolyte, which is found to proceed by 3D instantaneous nucleation, is polarized to high cathodic potentials and grows into 3D progressive nucleation and diffusion-controlled growth in high concentration cyanide electrolyte.

Orijinal dilİngilizce
Sayfa (başlangıç-bitiş)378-392
Sayfa sayısı15
DergiTurkish Journal of Chemistry
Hacim44
Basın numarası2
DOI'lar
Yayın durumuYayınlandı - 2020

Bibliyografik not

Publisher Copyright:
© TÜBİTAK

Finansman

The authors would like to thank TÜBİTAK (The Scientific and Technological Research Council of Turkey) for supporting Hatice Kübra Akben with TÜBİTAK-BİDEB Ph.D. scholarship.

FinansörlerFinansör numarası
Türkiye Bilimsel ve Teknolojik Araştirma Kurumu

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