Kinetic Fractionation of Antimony Isotopes during Reduction by Sulfide

15 September 2023, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Stable isotope ratios of antimony (Sb) in the environment can provide valuable information on sources and processes such as redox transformations. To investigate the fractionation when Sb(V) is chemically reduced by sulfide to Sb(III), experiments with 0.008 to 0.01 mM Sb(V) and 0.009 to 6 mM sulfide at a pH of 1 to 8 were performed. Experiments at pH 1 to 6 precipitated Sb2S3, while at pH 7 to 8 Sb(III) remained in solution. The Sb(III) product was enriched in the lighter isotope. The isotopic fractionation (ε ≈ δinstantaneous product – δreactant) for the pH 1 experiment was -1.42 ± 0.04‰ while the pH 5 to 8 experiments ranged from -0.46 ± 0.04‰ to -0.62 ± 0.04‰. The small magnitude of fractionation observed in experiments at circumneutral pH may decrease the utility of Sb isotope measurement as reduction indicators in natural systems, as adsorption of Sb has been shown to fractionate isotopes in the same direction and similar magnitude (up to 1.14‰) (Wasserman, 2020; Zhou et al., 2023).

Keywords

Antimony
Isotope
Redox
Sulfide
Fractionation

Supplementary materials

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Supporting Info (1)
Description
Table of Sb concentration and isotope data for all experiments; first-order rate law slopes; Rayleigh distillation model for pH 8 and 2 mM experiment using Sb(V) and Sb(III) data (PDF).
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