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University of Illinois at Urbana-Champaign

Kinetic fractionation of antimony isotopes during reduction by sulfide

Abstract

dc:description

Antimony (Sb) is a toxic metalloid that enters the environment through both natural processes and anthropogenic input. Despite Sb’s increasing use, a limited number of studies exist on its mobility, toxicity, and geochemical reactions. Stable isotope ratios of elements in the environment can provide valuable information on sources and processes such as redox transformations, precipitation, and adsorption. Isotope ratio measurements can be used to determine the extent of reaction with better accuracy than concentration measurements and without complications caused by dilution and adsorption. However, this requires knowledge of the difference between the reactant and product isotope ratios, or fractionation factor, and laboratory studies are needed to determine fractionation factors for various relevant reactions at varying reaction conditions. Given that Sb isotopes have not been developed until recently, isotope fractionation factors for most processes of Sb are still unknown. Redox reactions are typically the most significant sources of isotopic fractionation in natural systems. The oxidation state of Sb in the environment influences it’s mobility, with Sb(III) being less mobile than Sb(V). To investigate the fractionation when Sb(V) (+5 valence) is chemically reduced by sulfide to Sb(III) (+3 valence), controlled experiments with 0.01 mM Sb(V) and 2 to 6 mM sulfide at a pH of 6 and 7 were performed. Anion exchange was used to separate Sb(V) from Sb(III), and isotope ratios were analyzed using hydride generation MC-ICP-MS. The fractionation (ε) values for pH 6/High H2S, pH 7/High H2S and pH 7/Low H2S were -0.45 ± 0.03 ‰, -0.36 ± 0.05 ‰, and -0.57 ± 0.03‰, respectively. This provides important fundamental knowledge of a major driver of Sb isotope variation in nature and will be used as Sb isotopes are developed for use in modern environmental monitoring efforts and as a proxy for paleo-redox conditions.

Degree

thesis:*
Name thesis:degree_name
M.S.
Level thesis:degree_level
Thesis
Discipline thesis:degree_discipline
Geology
Grantor
University of Illinois at Urbana-Champaign
Year dc:date
2022

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Veldhuizen, Hannah Juliette
Contributors dc:contributor
  • Johnson, Thomas M

Subjects

dc:subject × 2

Rights

dc:rights
Statement dc:rights
  • Copyright 2022 Hannah Veldhuizen
Language dc:language
en, eng

Identifiers

dc:identifier.*
Handle dc:identifier
https://hdl.handle.net/2142/115586

Chain of custody

source
Harvested from
University of Illinois - Urbana-Champaign
Base URL
www.ideals.illinois.edu/oai-pmh
Last updated
2026-07-22
Source record
OAI-PMH GetRecord
related terms
citation

Veldhuizen, Hannah Juliette. Kinetic fractionation of antimony isotopes during reduction by sulfide. Thesis thesis, University of Illinois at Urbana-Champaign, 2022. https://hdl.handle.net/2142/115586