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Published on: December 5, 2019
Antimony sorption to schwertmannite in acid sulfate environments
Mohammad Rastegari1, Niloofar Karimian2, Scott G Johnston3
1Faculty of Science and Engineering, Southern Cross University, Lismore, NSW 2480, Australia.
Schwertmannite immobilizes antimony(V) by incorporating it into its crystal structure through substitution, enhancing mineral stability. This process is effective even at high antimony loadings and resistant to phosphate.
Area of Science:
- Environmental Geochemistry
- Mineralogy
- Environmental Science
Background:
- Schwertmannite, an iron(III) oxyhydroxysulfate mineral, influences antimony(V) mobility in acidic sulfate environments.
- Understanding Sb(V) uptake mechanisms by schwertmannite is crucial for acid mine drainage and acid sulfate soil remediation.
Purpose of the Study:
- To investigate the mechanisms of aqueous antimony(V) sorption onto schwertmannite.
- To determine the role of schwertmannite in controlling Sb(V) mobility in acidic sulfate conditions.
Main Methods:
- Examined Sb(V) sorption to schwertmannite at environmentally relevant loadings and pH 3 in sulfate-rich solutions.
- Utilized Antimony K-edge extended X-ray absorption fine structure (EXAFS) spectroscopy to analyze Sb(V) coordination and linkages.
Main Results:
- Sb(V) sorption occurred via edge and double-corner sharing linkages, indicating heterovalent Sb(V)-for-Fe(III) substitution within the schwertmannite structure.
- Sb(V) sorption was not limited by surface complexation sites and showed strong resistance to desorption by phosphate.
- Sorption of Sb(V) enhanced schwertmannite stability, reducing its dissolution rate.
Conclusions:
- Schwertmannite immobilizes Sb(V) by incorporating it into its crystal structure, not just surface complexation.
- This mechanism highlights schwertmannite's significant role in sequestering Sb(V) in acidic sulfate environments.
- The findings have implications for understanding and managing antimony contamination in acid mine drainage and soils.
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