Thiol functionalized activated carbon for gold thiosulfate recovery, an analysis of the interactions between gold and sulfur functions
Cyanide salts are currently used as leaching agents in gold extraction processes despite their toxicity. Thiosulfate is a greener choice, but its employment is constrained by the difficulty at recovering gold thiosulfate from the leachate using activated carbon, which in contrast, works well for gol...
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Published in | Carbon (New York) Vol. 204; pp. 254 - 267 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier Ltd
01.02.2023
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Subjects | |
Online Access | Get full text |
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Summary: | Cyanide salts are currently used as leaching agents in gold extraction processes despite their toxicity. Thiosulfate is a greener choice, but its employment is constrained by the difficulty at recovering gold thiosulfate from the leachate using activated carbon, which in contrast, works well for gold-cyanide adsorption. Aiming to solve this problem, activated carbon has been covalently functionalized with thiol groups (-SH) through a peptide bond formation with cysteamine, as thiol-carrier molecule. The functionalized carbon accomplishes up to 100% Au recovery (with 2 and 25 ppm Au solution) in 8 h contact and its performance seems independent on the solution's pH. In-depth solid characterization techniques (XPS, TOF-SIMS, FTIR, PXRD, TEM, N₂ physisorption, elemental analysis) have been used to unravel the interactions between Au thiosulfate and thiol functions and two different gold adsorption mechanisms have been demonstrated: under acid conditions, the formation of Au1+- S chains has been proven. Under basic conditions, Au⁰ species have been detected in addition to Au1+- S chains. Elution of the gold loaded samples has been accomplished at a 71% level using Na₂S₂O₃ and NH₄OH as eluents.
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•Active carbon is covalently functionalized with thiol groups.•The S-rich carbon recovers up to 100% of Au thiosulfate in 8 h contact.•Au1+-S chains formation is proven as adsorption mechanism in acid conditions.•Under basic conditions, Au⁰ species are evidenced in addition to Au1+-S chains.•Elution is accomplished up to 71% using Na₂S₂O₃ and NH₄OH. |
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ISSN: | 0008-6223 1873-3891 |
DOI: | 10.1016/j.carbon.2022.12.061 |