Uranium: the leach–IX/SX–precipitate family
The uranium flowsheet assembled from mechanisms taught earlier: leaching by tank, heap or in-situ recovery, concentration and purification by ion exchange or solvent extraction, and precipitation of the uranium concentrate. A process-description survey only.
The idea
Uranium is recovered by a leach–concentrate–precipitate flowsheet that composes from mechanisms taught earlier. This page assembles them as a process-description survey, naming each contribution rather than re-teaching it.
The flowsheet in one line
Leach the uranium into solution, concentrate and purify it from a dilute liquor by ion exchange or solvent extraction, and precipitate it as a uranium concentrate: leach–IX/SX–precipitate.
What each stage is doing
The leach can take any of three contacting forms taught earlier — stirred-tank leaching (topic 4.3), heap leaching (topic 4.4) or in-situ recovery, leaching the orebody in place through wells (topic 4.5) — in either an acid (sulfuric) or an alkaline (carbonate) lixiviant, chosen on the gangue. Concentration is ion exchange (topic 6.7) or solvent extraction (topic 6.6): the uranium is loaded from a large, dilute, impure leach liquor onto a resin or into an organic, then stripped into a small, clean, concentrated solution — ion exchange being the classic choice precisely because it pulls a target from a very low tenor where SX’s economics fail. Precipitation is pH control, topic 6.2: the purified solution is precipitated to a solid uranium concentrate that is dried for transport.
The defining numbers
The leach reagent demand lands on the leach reagent consumption calculator below, and the acid-leach lixiviant reads on the sulfuric acid hub. The IX and SX concentration steps are read on their own mechanisms — the load–wash–elute–regenerate cycle and the O/A ratio — rather than a single committed calculation, which is why the page leans on the cross-links into topics 6.6 and 6.7.
Where it differs from the others
Uranium is the family that most often reaches for ion exchange, and the one that can leach the orebody in place rather than mining it — the in-situ route. Its product is a precipitated concentrate, not a metal; its defining engineering problem is recovering a low-tenor value cleanly from a large, dilute flow, which is exactly the duty ion exchange was built for.
Diagram
Go deeper
- Leach reagent consumption calculator →Calculator
Work the leach reagent demand from the ore feed rate and the dose per tonne for the acid or alkaline leach.
- Sulfuric acid hub →Substance hub
Read the sulfuric acid property data behind the acid-leach lixiviant.
Sources
- •International Atomic Energy Agency, Uranium Extraction Technology, Technical Reports Series No. 359, 1993.
- •Merritt, R.C., The Extractive Metallurgy of Uranium, Colorado School of Mines Research Institute, 1971.
- •Free, M.L., Hydrometallurgy: Fundamentals and Applications, 2013.
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