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Updated: Sep 18, 2025

Two-way Valorization of Blast Furnace Slag: Synthesis of Precipitated Calcium Carbonate and Zeolitic Heavy Metal Adsorbent
Published on: February 21, 2017
Geochemical factors governing vanadium speciation and mobilisation in technosol eco-engineered from bauxite residue
Narottam Saha1, Chengyao Ren1, David Parry2
1Sustainable Minerals Institute, The University of Queensland, Brisbane, QLD 4072, Australia.
Abstract:
The high solubility of oxyanions, such as vanadium (V), in alkaline (pH > 9) bauxite residue (BR) generated from alumina production is one of the major environmental risks associated with BR management. Ecological engineering of BR into soil-like growth media (i.e., technosol) offers a promising solution by irreversibly neutralising alkalinity and improving geochemical stability. However, the mechanisms governing the V fractionation, potential mobility, and bioavailability during this transformation remain poorly understood. Here, we show that in a long-term field lysimeter trial, V in BR technosol is primarily hosted in Fe oxide minerals, particularly hematite, of residual phase, followed by organic and oxide-bound phases. The pH was the key driver controlling V solubility, suggesting the importance of irreversible neutralisation of alkalinity in BR using effective eco-engineering inputs (e.g., organic matter and fertiliser). Co-amendments with organic matter and superphosphate fertiliser were most effective in achieving pH neutralisation and V immobilisation. Organic-V complexation in the OM-treated BR can act as an important sink to immobilise V. Consequently, the long-term pollution risk associated with V in BR technosol is expected to be minimal as the technosol system progressively develops into a stable, circumneutral pH, with soil-like properties capable of supporting long-term vegetation growth.
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