GB746780A - Improvements in or relating to hydrometallurgy of nickel and cobalt - Google Patents

Improvements in or relating to hydrometallurgy of nickel and cobalt

Info

Publication number
GB746780A
GB746780A GB24669/53A GB2466953A GB746780A GB 746780 A GB746780 A GB 746780A GB 24669/53 A GB24669/53 A GB 24669/53A GB 2466953 A GB2466953 A GB 2466953A GB 746780 A GB746780 A GB 746780A
Authority
GB
United Kingdom
Prior art keywords
cobalt
nickel
carbonate
solution
ratio
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.)
Expired
Application number
GB24669/53A
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.)
Chemical Construction Corp
Original Assignee
Chemical Construction Corp
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 Chemical Construction Corp filed Critical Chemical Construction Corp
Publication of GB746780A publication Critical patent/GB746780A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01GCOMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G51/00Compounds of cobalt
    • C01G51/06Carbonates

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Manufacture And Refinement Of Metals (AREA)

Abstract

Substantially cobalt-free nickel-bearing solutions are recovered from liquor containing both metals in the form of sulphates or carbonates by adjusting the metal content of the liquor to up to 100 grams/litre of dissolved cobalt plus nickel for carbonate solutions and up to 135 grams/litre for sulphate solutions, 1-4 mols of amonium carbonate per mol of dissolved cobalt plus nickel salts and sufficient available ammonia to retain cobalt and nickel in solution under atmospheric conditions, heating the solution under pressure to above 140 DEG C. till precipitation substantially ceases and separating the precipitate containing cobalt carbonate from the solution. Where the nickel : cobalt ratio in the liquor is less than 1 the treatment may take place in two stages, a substantially nickel-free cobalt precipitate being obtained in the first stage, the precipitation in the second stage being continued till the solution is substantially cobalt free. Heating preferably takes place in an atmosphere of hydrogen. In carbonate solutions the mol ratio of free ammonia : dissolved nickel and cobalt may be 1.5-2.0 but is preferably higher and up to 4.0, a good range being 2.5-3.5. To ensure selective precipitation the solution should contain a proportion of ammonium carbonate which varies with the ratio of nickel : cobalt, the mol ratio of ammonium carbonate : nickel + cobalt being, for example 1 : 1 when the nickel:cobalt ratio is 1.5 or lower and 3:1 or 4:1 when the nickel:cobalt ratio is higher. The proportions given above are varied slightly in sulphate solution. The cobalt carbonate precipitate and the residual solution may be separately treated to recover the metals in metallic form. (See Group II.)ALSO:Cobalt carbonate precipitated from a nickel-and cobalt-containing solution (see Group III) is treated to recover cobalt as metal by slurrying the carbonate in water to form a 25-40 per cent slurry and subjected to an elevated temperature of 100 DEG F. to 500 DEG F. or above, preferably 200-450 DEG F., and to a partial pressure of at least 100 lbs./sq. in. gauge of a non-sulphidising reducing gas such as hydrogen. The resulting slurry of cobalt metal is cooled and the metal powder dried. The solution resulting from cobalt carbonate precipitation may be treated to recover nickel and any residual cobalt as metals by adjusting the ammonia and carbonate contents and treating the liquor at different but increasing elevated temperatures with a reducing gas to recover a low cobalt-content nickel powder and finally a low nickel-content cobalt powder.
GB24669/53A 1952-09-23 1953-09-07 Improvements in or relating to hydrometallurgy of nickel and cobalt Expired GB746780A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US746780XA 1952-09-23 1952-09-23

Publications (1)

Publication Number Publication Date
GB746780A true GB746780A (en) 1956-03-21

Family

ID=22120982

Family Applications (1)

Application Number Title Priority Date Filing Date
GB24669/53A Expired GB746780A (en) 1952-09-23 1953-09-07 Improvements in or relating to hydrometallurgy of nickel and cobalt

Country Status (1)

Country Link
GB (1) GB746780A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008049177A2 (en) * 2006-10-27 2008-05-02 Companhia Vale Do Rio Doce Method for production of metallic cobalt from the nickel solvent extraction raffinate
CN113242908A (en) * 2018-11-26 2021-08-10 巴斯夫欧洲公司 Battery recovery by hydrogen injection into leachate

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008049177A2 (en) * 2006-10-27 2008-05-02 Companhia Vale Do Rio Doce Method for production of metallic cobalt from the nickel solvent extraction raffinate
WO2008049177A3 (en) * 2006-10-27 2008-07-03 Vale Do Rio Doce Co Method for production of metallic cobalt from the nickel solvent extraction raffinate
GB2456701A (en) * 2006-10-27 2009-07-29 Vale Do Rio Doce Co Method for production of metallic cobalt from the nickel solvent extraction raffinate
GB2456701B (en) * 2006-10-27 2012-01-18 Vale Do Rio Doce Co Method for production of metallic cobalt from the nickel solvent extraction raffinate
CN113242908A (en) * 2018-11-26 2021-08-10 巴斯夫欧洲公司 Battery recovery by hydrogen injection into leachate

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