Selective sorption-based separation of palladium from process solutions using chemically modified silica

This study focuses on investigating the possibility of selective separation of palladium (II) from solutions containing non-ferrous metals and iron by sorption onto chemically modified silica. The study used both individual (single-metal) and model multicomponent solutions. The sorbents included silicas functionalized with iminodiacetic acid (IDA-D), phosphonic acid (PA-D), and aminomethylphosphonic acid (AMPA-D) groups, as well as a well-known chemically modified silica bearing grafted γ-aminopropyltriethoxysilane (APTES) groups at a grafting density of 1.63 mmol/g. Under static conditions at room temperature, the time required to reach equilibrium sorption values for Cu(II), Ni(II), and Fe(III) ions – typically present in process solutions – was determined for the IDA-D, PA-D, and AMPA-D sorbents. Sorption dependencies on hydrochloric acid concentration were established for these metal ions. For IDA-D, the effect of halide ion concentration on sorption was also studied. It was shown that these ions are sorbed in weakly acidic media but not in 1–2 M HCl, and that sorption capacity decreases in the order: IDA-D > AMPA-D > PA-D. However, the conclusion that quantitative separation of Pd(II) from base metal ions could be achieved using these complexing sorbents (exemplified by IDA-D) under dynamic conditions was not confirmed. The sorption behavior of Pd(II), Cu(II), and Al(III) ions was also examined under static and dynamic conditions using the APTES-functionalized silica and chloride and chloride-bromide solutions, including model solutions simulating leach liquors generated from the treatment of spent catalysts for low-temperature carbon monoxide oxidation. These solutions contained 0.004–0.015 mol/L Pd, 0.014–0.049 mol/L Cu, and 0.015–0.060 mol/L Al. The results demonstrated the feasibility of selectively separating Pd(II) from leach solutions of spent catalysts using this sorbent. A processing scheme was proposed, comprising sorption from 0.1 M HCl, water rinsing of the loaded sorbent, and elution of Pd(II) with a 5 % thiourea solution in 0.1 M HCl. It was shown that separation of palladium from non-ferrous metals occurs already at the sorption and washing stages.

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Publication Details

Journal
Izvestiya Non-Ferrous Metallurgy
Published
2025-06-27
DOI
https://doi.org/10.17073/0021-3438-2025-2-41-54
Primary Topic
Extraction and Separation Processes
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article
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article

Selective sorption-based separation of palladium from process solutions using chemically modified silica

T. M. Buslaeva, П. Г. Мингалев, Е. В. Волчкова, I. V. Boryagina
Izvestiya Non-Ferrous Metallurgy
Extraction and Separation Processes
article

Selective sorption-based separation of palladium from process solutions using chemically modified silica

T. M. Buslaeva, П. Г. Мингалев, Е. В. Волчкова, I. V. Boryagina
article en

Abstract

This study focuses on investigating the possibility of selective separation of palladium (II) from solutions containing non-ferrous metals and iron by sorption onto chemically modified silica. The study used both individual (single-metal) and model multicomponent solutions. The sorbents included silicas functionalized with iminodiacetic acid (IDA-D), phosphonic acid (PA-D), and aminomethylphosphonic acid (AMPA-D) groups, as well as a well-known chemically modified silica bearing grafted γ-aminopropyltriethoxysilane (APTES) groups at a grafting density of 1.63 mmol/g. Under static conditions at room temperature, the time required to reach equilibrium sorption values for Cu(II), Ni(II), and Fe(III) ions – typically present in process solutions – was determined for the IDA-D, PA-D, and AMPA-D sorbents. Sorption dependencies on hydrochloric acid concentration were established for these metal ions. For IDA-D, the effect of halide ion concentration on sorption was also studied. It was shown that these ions are sorbed in weakly acidic media but not in 1–2 M HCl, and that sorption capacity decreases in the order: IDA-D > AMPA-D > PA-D. However, the conclusion that quantitative separation of Pd(II) from base metal ions could be achieved using these complexing sorbents (exemplified by IDA-D) under dynamic conditions was not confirmed. The sorption behavior of Pd(II), Cu(II), and Al(III) ions was also examined under static and dynamic conditions using the APTES-functionalized silica and chloride and chloride-bromide solutions, including model solutions simulating leach liquors generated from the treatment of spent catalysts for low-temperature carbon monoxide oxidation. These solutions contained 0.004–0.015 mol/L Pd, 0.014–0.049 mol/L Cu, and 0.015–0.060 mol/L Al. The results demonstrated the feasibility of selectively separating Pd(II) from leach solutions of spent catalysts using this sorbent. A processing scheme was proposed, comprising sorption from 0.1 M HCl, water rinsing of the loaded sorbent, and elution of Pd(II) with a 5 % thiourea solution in 0.1 M HCl. It was shown that separation of palladium from non-ferrous metals occurs already at the sorption and washing stages.

Izvestiya Non-Ferrous Metallurgy(2)
MIREA - Russian Technological University (RU), Moscow State University (TJ)
Openalex Percentile: Top 85%
Extraction and Separation Processes
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