GB2198723A - Separating uranium from uranium bearing materials - Google Patents

Separating uranium from uranium bearing materials Download PDF

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Publication number
GB2198723A
GB2198723A GB08728419A GB8728419A GB2198723A GB 2198723 A GB2198723 A GB 2198723A GB 08728419 A GB08728419 A GB 08728419A GB 8728419 A GB8728419 A GB 8728419A GB 2198723 A GB2198723 A GB 2198723A
Authority
GB
United Kingdom
Prior art keywords
uranium
process according
slurry
sulphur dioxide
oxygen
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
GB08728419A
Other versions
GB8728419D0 (en
Inventor
Ronald David Hancock
Wasyl Michael Sajik
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BP PLC
Original Assignee
BP PLC
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by BP PLC filed Critical BP PLC
Publication of GB8728419D0 publication Critical patent/GB8728419D0/en
Publication of GB2198723A publication Critical patent/GB2198723A/en
Withdrawn legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B60/00Obtaining metals of atomic number 87 or higher, i.e. radioactive metals
    • C22B60/02Obtaining thorium, uranium, or other actinides
    • C22B60/0204Obtaining thorium, uranium, or other actinides obtaining uranium
    • C22B60/0217Obtaining thorium, uranium, or other actinides obtaining uranium by wet processes
    • C22B60/0221Obtaining thorium, uranium, or other actinides obtaining uranium by wet processes by leaching
    • C22B60/0226Obtaining thorium, uranium, or other actinides obtaining uranium by wet processes by leaching using acidic solutions or liquors
    • C22B60/0234Obtaining thorium, uranium, or other actinides obtaining uranium by wet processes by leaching using acidic solutions or liquors sulfurated ion as active agent
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01GCOMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G43/00Compounds of uranium

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  • Chemical & Material Sciences (AREA)
  • General Life Sciences & Earth Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Geology (AREA)
  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Environmental & Geological Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Manufacture And Refinement Of Metals (AREA)
  • Inorganic Compounds Of Heavy Metals (AREA)

Abstract

Uranium is separated from uranium bearing materials by treating the material with a mineral acid to form a slurry and passing a mixture of sulphur dioxide and oxygen containing gas into the slurry. The uranium solution is then separated from the residual ore material. The mineral acid is suitably dilute sulphuric acid and the volume ratio of sulphur dioxide to oxygen is suitably in the range 1:2 to 1:20.

Description

PROCESS FOR SEPARATING URANIUM FROM URANIUM BEARING MATERIALS The present invention relates to a process for the separation of uranium from uranium bearing materials.
Most uranium minerals are friable and in general are not effectively separated from the gangue or waste constituents by physical methods such as flotation. Uranium can be dissolved from its ores by mineral acids and if uranium is present in the ore in its lower valency reduced state, as is usual, an oxidising agent must also be used in the dissolution process. The most commonly used oxidising agents are manganese dioxide (pyrolusite), sodium chlorate, hydrogen peroxide and Caro's acid.
The present invention relates to a novel process for the separation of uranium from uranium bearing materials that has advantages over known processes under certain conditions.
Thus according to thapresent invention there is provided a process for the separation of uranium from uranium bearing materials comprising the steps of (a) treating the material with a mineral acid to form a slurry, (b) passing a mixture of sulphur dioxide and an oxygen containing gas into the slurry so as to convert the uranium into its higher oxidation state thereby rendering the uranium soluble, and (c) extracting the uranium by a conventional technique. The steps may be performed simultaneously or sequentially.
The mineral acid is suitably dilute sulphuric acid and the mixture of sulphur dioxide to oxygen is suitably in the volume ratio 1:2 to 1:20.
While not wishing to be bound by any theory, as iron containing minerals invariably occur with the uranium ore and sufficient amounts of this iron are soluble in the mineral acid, the function of the added oxidant is generally believed to be the oxidation of ferrous ion to ferric ion, the latter sometimes being referred to as the 'true' uranium oxidant (U4+ + 2Fe3+
U6+ + 2Fe2+).
The action of sulphur dioxide/oxygen containing gas mixtures in effecting this process is surprising as oxygen itself is not a sufficiently strong oxidant for this conversion and sulphur dioxide is well known as a reducing agent.
The invention will now be described by way of example only.
After mining, the uranium ore is crushed and ground and is then leached for several hours in a dilute acid solution through which a sulphur dioxide/oxygen mixture is bubbled. The volume ratio of sulphur dioxide:oxygen is 1:10. The temperature of the slurry may be ambient but elevated temperatures are preferred, e.g. 80 to 950C.
Following the dissolution of the uranium, the uranium bearing solution may be separated from the residual ore solids e.g. by filtration. The solution is then further purified by ion exchange or solvent extraction to obtain uranium of sufficient purity.
Alternatively the slurry may be treated directly e.g. by contact with suitable resins.
The sulphur dioxide and oxygen are suitably pre-mixed and emerge into the solution~by use of a sparge tube.

Claims (11)

Claims:
1. A process for the separation of uranium from uranium bearing materials comprising the steps of (a) treating the material with a mineral acid to form a slurry, (b) passing a mixture of sulphur dioxide and an oxygen containing gas into the slurry so as to convert the uranium into its highest oxidation state thereby rendering the uranium soluble, and (c) extracting the uranium by a conventional technique.
2. A process according to claim 1 in which the steps are performed simultaneously.
3. A process according to claim 1 in which the steps are performed sequentially.
4. A process according to any of the preceding claims in which the volume ratio of sulphur dioxide to oxygen is in the range 1:2 to 1:20.
5. A process according to any of the preceding claims in which the volume ratio of sulphur dioxide to oxygen is 1:10.
6. A process according to any of the preceding claims in which the temperature of the slurry is above ambient temperature.
7. A process according to any of the preceding claims in which the temperature of the slurry is 800C and 950C.
8. A process according to any of the preceding claims in which the resultant uranium bearing solution is separated from the residual ore solids by filtration.
9. A process according to claim 8 in which the separated uranium bearing solution is further purified to obtain uranium by ion-exchange or solvent extraction.
A A process according to any of claims 1 to 7 in which the resultant uranium bearing solution with the residual ore solids is treated with ion exchange resins to recover uranium.
11. A process for separation of uranium from uranium bearing materials as hereinbefore described and with reference to the examples.
GB08728419A 1986-12-18 1987-12-04 Separating uranium from uranium bearing materials Withdrawn GB2198723A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB868630316A GB8630316D0 (en) 1986-12-18 1986-12-18 Separation process

Publications (2)

Publication Number Publication Date
GB8728419D0 GB8728419D0 (en) 1988-02-10
GB2198723A true GB2198723A (en) 1988-06-22

Family

ID=10609249

Family Applications (2)

Application Number Title Priority Date Filing Date
GB868630316A Pending GB8630316D0 (en) 1986-12-18 1986-12-18 Separation process
GB08728419A Withdrawn GB2198723A (en) 1986-12-18 1987-12-04 Separating uranium from uranium bearing materials

Family Applications Before (1)

Application Number Title Priority Date Filing Date
GB868630316A Pending GB8630316D0 (en) 1986-12-18 1986-12-18 Separation process

Country Status (1)

Country Link
GB (2) GB8630316D0 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3922866A1 (en) * 1988-08-01 1990-02-08 Draftex Ind Ltd SEALING STRIP
FR2716683A1 (en) * 1994-02-25 1995-09-01 Boc Gases Australia Ltd Uranium extraction process.
WO2011116426A1 (en) * 2010-03-24 2011-09-29 Bhp Billiton Olympic Dam Corporation Pty Ltd Process for leaching refractory uraniferous minerals

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB760191A (en) * 1953-10-20 1956-10-31 Mini Of Mines And Technical Su Sulphur dioxide leaching of uranium containing material
EP0113649A1 (en) * 1982-12-09 1984-07-18 Boliden Aktiebolag A method for working-up complex sulphidic ore concentrates

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB760191A (en) * 1953-10-20 1956-10-31 Mini Of Mines And Technical Su Sulphur dioxide leaching of uranium containing material
EP0113649A1 (en) * 1982-12-09 1984-07-18 Boliden Aktiebolag A method for working-up complex sulphidic ore concentrates

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
WO 85/01300 *

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3922866A1 (en) * 1988-08-01 1990-02-08 Draftex Ind Ltd SEALING STRIP
DE3922866C2 (en) * 1988-08-01 2001-11-22 Gencorp Property Inc Sealing strips
FR2716683A1 (en) * 1994-02-25 1995-09-01 Boc Gases Australia Ltd Uranium extraction process.
WO2011116426A1 (en) * 2010-03-24 2011-09-29 Bhp Billiton Olympic Dam Corporation Pty Ltd Process for leaching refractory uraniferous minerals

Also Published As

Publication number Publication date
GB8728419D0 (en) 1988-02-10
GB8630316D0 (en) 1987-01-28

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Legal Events

Date Code Title Description
WAP Application withdrawn, taken to be withdrawn or refused ** after publication under section 16(1)