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Updated: Mar 12, 2026

Atomic Layer Deposition of Vanadium Dioxide and a Temperature-dependent Optical Model
Published on: May 23, 2018
Vanadium sorption by mineral soils: Development of a predictive model
Maja A Larsson1, Golshid Hadialhejazi2, Jon Petter Gustafsson3
1Department of Soil and Environment, Swedish University of Agricultural Sciences, Box 7014, 750 07, Uppsala, Sweden.
Vanadium sorption in soils is key to its toxicity. This study developed a model predicting vanadium sorption strength, revealing current environmental guidelines may be inadequate.
Area of Science:
- Environmental Science
- Soil Chemistry
- Geochemistry
Background:
- Vanadium toxicity in soils is influenced by its sorption behavior.
- Understanding vanadium sorption is crucial for assessing soil contamination and plant uptake.
Purpose of the Study:
- To investigate vanadate(V) sorption properties across 26 diverse mineral soils.
- To develop and optimize a predictive model for vanadium sorption based on soil properties and pH.
- To evaluate the adequacy of current environmental guidelines for vanadium.
Main Methods:
- Utilized Freundlich equation with a pH term to model vanadium sorption.
- Employed Vanadium K-edge XANES spectroscopy to identify vanadium speciation in selected soils.
- Measured pH-dependent vanadium solubility and calculated the Freundlich Sorption Strength (FSS).
Main Results:
- The developed model accurately predicted vanadium sorption for most soils (r² > 0.99 for 20/26 soils).
- Vanadium primarily sorbed as adsorbed vanadate(V) onto Fe and Al hydrous oxides.
- A strong correlation (r² = 0.85) was observed between FSS and oxalate-extractable Fe and Al.
- Calculated FSS values varied significantly, indicating potential issues with existing environmental guidelines.
Conclusions:
- The developed model provides a robust framework for predicting vanadium sorption in mineral soils.
- Soil iron and aluminum content are critical factors controlling vanadium sorption.
- Current environmental guidelines for vanadium may require revision due to the wide range of predicted sorption strengths and potential under- or overprotection.
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