Recovery of Pt, Pd and Au from a cyanide solution through a carbon adsorption and elution process

In order to exploit lower grade and complex platinum group metal resources, cheaper and more efficient alternatives to the conventional mill-float-smelt-refine route are being sought, particularly for resources' in areas that are water-scarce and where electrification is costly and problematic....

Full description

Bibliographic Details
Main Authors: Snyders, C., Bradshaw, S., Akdogan, G., Mpinga, C., Wyk, A., Eksteen, Jacques
Format: Conference Paper
Published: Gecamin 2014
Online Access:http://hdl.handle.net/20.500.11937/13101
_version_ 1848748258450472960
author Snyders, C.
Bradshaw, S.
Akdogan, G.
Mpinga, C.
Wyk, A.
Eksteen, Jacques
author_facet Snyders, C.
Bradshaw, S.
Akdogan, G.
Mpinga, C.
Wyk, A.
Eksteen, Jacques
author_sort Snyders, C.
building Curtin Institutional Repository
collection Online Access
description In order to exploit lower grade and complex platinum group metal resources, cheaper and more efficient alternatives to the conventional mill-float-smelt-refine route are being sought, particularly for resources' in areas that are water-scarce and where electrification is costly and problematic. Leaching with cyanide is a promising process option and although recoveries are lower than in the conventional process routes, progress into the understanding of cyanide leaching of PGM containing ore and concentrate has been made. Research regarding the feasibility of upgrading the pregnant PGM leach solution using activated carbon has, however, been lacking and hence forms the focus of this paper. Bottle roll adsorption tests for dilute PGM solutions (0.15ppm Pt, 0.38 ppm Pd, 0.1 ppm Au) onto granular activated carbon showed high rates within the first 60 minutes (giving more than 90% recovery of precious metals). Comparison of the Pt isotherm to Au isotherms from literature indicated a similar loading capacity, while that of Pd was found to be significantly lower. The effects of solution pH, temperature, base metal concentration, free cyanide concentration, thiocyanate concentration, initial PGM concentration and activated carbon concentration were investigated and are discussed. Elution of the Pt and Pd, with the AARL elution process, was found to be effective with recoveries of 95% after 5 bed volumes of eluant at the optimum pre-treatment concentrations and a temperature of 80°C. Temperature, NaCN and NaOH pre-treatment concentration and the ionic strength of the eluant were found to be the most important factors affecting elution while base metals concentration, acid-pre-treatment, carbon loading and thiocyanate concentrations to a lesser extent. Simplified combined flow sheets are suggested and the corresponding mass balances are compared.
first_indexed 2025-11-14T07:02:11Z
format Conference Paper
id curtin-20.500.11937-13101
institution Curtin University Malaysia
institution_category Local University
last_indexed 2025-11-14T07:02:11Z
publishDate 2014
publisher Gecamin
recordtype eprints
repository_type Digital Repository
spelling curtin-20.500.11937-131012017-01-30T11:34:50Z Recovery of Pt, Pd and Au from a cyanide solution through a carbon adsorption and elution process Snyders, C. Bradshaw, S. Akdogan, G. Mpinga, C. Wyk, A. Eksteen, Jacques In order to exploit lower grade and complex platinum group metal resources, cheaper and more efficient alternatives to the conventional mill-float-smelt-refine route are being sought, particularly for resources' in areas that are water-scarce and where electrification is costly and problematic. Leaching with cyanide is a promising process option and although recoveries are lower than in the conventional process routes, progress into the understanding of cyanide leaching of PGM containing ore and concentrate has been made. Research regarding the feasibility of upgrading the pregnant PGM leach solution using activated carbon has, however, been lacking and hence forms the focus of this paper. Bottle roll adsorption tests for dilute PGM solutions (0.15ppm Pt, 0.38 ppm Pd, 0.1 ppm Au) onto granular activated carbon showed high rates within the first 60 minutes (giving more than 90% recovery of precious metals). Comparison of the Pt isotherm to Au isotherms from literature indicated a similar loading capacity, while that of Pd was found to be significantly lower. The effects of solution pH, temperature, base metal concentration, free cyanide concentration, thiocyanate concentration, initial PGM concentration and activated carbon concentration were investigated and are discussed. Elution of the Pt and Pd, with the AARL elution process, was found to be effective with recoveries of 95% after 5 bed volumes of eluant at the optimum pre-treatment concentrations and a temperature of 80°C. Temperature, NaCN and NaOH pre-treatment concentration and the ionic strength of the eluant were found to be the most important factors affecting elution while base metals concentration, acid-pre-treatment, carbon loading and thiocyanate concentrations to a lesser extent. Simplified combined flow sheets are suggested and the corresponding mass balances are compared. 2014 Conference Paper http://hdl.handle.net/20.500.11937/13101 Gecamin restricted
spellingShingle Snyders, C.
Bradshaw, S.
Akdogan, G.
Mpinga, C.
Wyk, A.
Eksteen, Jacques
Recovery of Pt, Pd and Au from a cyanide solution through a carbon adsorption and elution process
title Recovery of Pt, Pd and Au from a cyanide solution through a carbon adsorption and elution process
title_full Recovery of Pt, Pd and Au from a cyanide solution through a carbon adsorption and elution process
title_fullStr Recovery of Pt, Pd and Au from a cyanide solution through a carbon adsorption and elution process
title_full_unstemmed Recovery of Pt, Pd and Au from a cyanide solution through a carbon adsorption and elution process
title_short Recovery of Pt, Pd and Au from a cyanide solution through a carbon adsorption and elution process
title_sort recovery of pt, pd and au from a cyanide solution through a carbon adsorption and elution process
url http://hdl.handle.net/20.500.11937/13101