Metal recovery from low concentration solutions using a flow-by reactor under galvanostatic approach
- Autores: Silva-Martínez S.1,2, Roy S.1
-
Afiliações:
- School of Chemical Engineering and Advanced Materials, Merz Court
- Research Center in Engineering and Applied Science
- Edição: Volume 52, Nº 1 (2016)
- Páginas: 71-77
- Seção: Article
- URL: https://journals.rcsi.science/1023-1935/article/view/187701
- DOI: https://doi.org/10.1134/S1023193516010092
- ID: 187701
Citar
Resumo
A recently proposed method using constant current steps were applied for a period of time on a reticulated vitreous carbon cathode. The current steps were calculated from a theoretical analysis of the metal concentration profile assuming that the metal was deposited under mass transport control. A model was developed to predict the concentration decay of metal ions during the process. The current required to reduce the metal at the mass transfer limit at each time step was predicted from the concentration decay obtained from the model. This process should enable one to maintain high metal recovery rates whilst maximizing current efficiency. This concept was tested on Cu(II) deposition from an acidified sulfate electrolyte using a flowby reactor system with a reticulated vitreous carbon electrode. The model was good for predicting copper metal removal using a three dimensional cathode in dilute rinse waters. Also, the predicted current efficiency was in good agreement with that obtained using the experimental data.
Palavras-chave
Sobre autores
S. Silva-Martínez
School of Chemical Engineering and Advanced Materials, Merz Court; Research Center in Engineering and Applied Science
Autor responsável pela correspondência
Email: ssilva@uaem.mx
Reino Unido da Grã-Bretanha e Irlanda do Norte, Newcastle, NE1 7RU; Av. Universidad 1001, Col. Chamilpa., Mexico, C.P. 62209
S. Roy
School of Chemical Engineering and Advanced Materials, Merz Court
Autor responsável pela correspondência
Email: s.roy@ncl.ac.uk
Reino Unido da Grã-Bretanha e Irlanda do Norte, Newcastle, NE1 7RU
Arquivos suplementares
