Experimental optimization of aurocyanide adsorption onto biomass activated carbon and re-examination of the adsorption mechanisms

dc.contributor.authorBediako, J.K.
dc.contributor.authorAffrifah, N.S.
dc.contributor.authorYun, Yeoung-Sang.
dc.contributor.authorRepo, E.
dc.date.accessioned2025-10-30T11:59:12Z
dc.date.issued2025-04-07
dc.descriptionResearch Article
dc.description.abstractActivated carbons (ACs) prepared from agricultural residues are ideal alternatives to the commercial coal-based ACs often applied in gold mining. Carbon activation using KOH produces high-quality carbons with good textural properties. Herein, fruit peel ACs were synthesized via KOH activation and evaluated for aurocyanide adsorption. The yield and adsorption capacity were optimized through a central composite design. The Langmuir maximum equilibrium uptake was 186.95 ± 16.44 mg/g. Re-examination of the adsorption mechanisms revealed that the presence of micro and mesopores, coupled with electrostatic binding, π–π interaction and ion-pair formations influenced the significantly high adsorption capacity. This study could be useful in the syntheses and application of agro waste-derived ACs as alternative adsorbents for gold recovery from aurocyanide leachates.
dc.description.sponsorshipThe authors acknowledge funding support from the Research Council of Finland (decision numbers: 330076 and 358148).
dc.identifier.citationBediako, J. K., Affrifah, N. S., Yun, Y. S., & Repo, E. (2025). Experimental optimization of aurocyanide adsorption onto biomass activated carbon and re-examination of the adsorption mechanisms. Minerals Engineering, 227, 109293.
dc.identifier.urihttps://doi.org/10.1016/j.mineng.2025.109293
dc.identifier.urihttps://ugspace.ug.edu.gh/handle/123456789/44104
dc.language.isoen
dc.publisherMinerals Engineering
dc.subjectBiomass
dc.subjectKOH activation
dc.subjectActivated carbon
dc.subjectAurocyanide
dc.subjectMechanism
dc.subjectIon pair
dc.titleExperimental optimization of aurocyanide adsorption onto biomass activated carbon and re-examination of the adsorption mechanisms
dc.typeArticle

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