Models for viscosity and density of copper electrorefining electrolytes

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Journal Title

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Volume Title

A1 Alkuperäisartikkeli tieteellisessä aikakauslehdessä

Date

2017

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Mcode

Degree programme

Language

en

Pages

15
1023-1037

Series

Physicochemical Problems of Mineral Processing, Volume 53, issue 2

Abstract

Viscosity and density of copper electrorefining electrolytes affect energy consumption and purity of cathode copper. Decreasing the viscosity and density increases the rate of falling of the anode slimes to the bottom of an electrorefining cell and increases the diffusivity and mobility of ions. Increasing the falling rate of the anode slimes decreases a risk of anode slime impurities ending up on the cathode and being entrapped into the copper deposit. This work introduces two new models for both viscosity and density of copper electrorefining electrolytes with high accuracy and one reconstructed improved model for some electrorefining data of viscosity published previously. The experimental work to build up these new models was carried out as a function of temperature (50, 60, 70 °C), copper (40, 50, 60 g/dm3), nickel (0, 10, 20 g/dm3) and sulfuric acid (130, 145, 160 g/dm3) concentrations for all models, and additionally arsenic concentration (0, 15, 30, 32, 64 g/dm3) was included in the viscosity models. Increasing concentrations of Cu, Ni, As and H2SO4 were found to increase the viscosity and density, whereas increasing temperature decreased both viscosity and density. The viscosity models were validated with industrial electrolyte samples from the Boliden Harjavalta Pori tankhouse. The experimental and modeling work carried out in this study resulted in improved viscosity models, having the strongest agreement with the industrial electrorefining electrolytes.

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Keywords

Copper electrorefining, Density model, Viscosity model

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Citation

Kalliomaki, T, Aji, A T, Rintala, L, Aromaa, J & Lundstrom, M 2017, ' Models for viscosity and density of copper electrorefining electrolytes ', Physicochemical Problems of Mineral Processing, vol. 53, no. 2, pp. 1023-1037 . https://doi.org/10.5277/ppmp170227