GB715243A - Nickel process - Google Patents

Nickel process

Info

Publication number
GB715243A
GB715243A GB1920252A GB1920252A GB715243A GB 715243 A GB715243 A GB 715243A GB 1920252 A GB1920252 A GB 1920252A GB 1920252 A GB1920252 A GB 1920252A GB 715243 A GB715243 A GB 715243A
Authority
GB
United Kingdom
Prior art keywords
nickel
ammonia
present
solids
ammonium carbonate
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
GB1920252A
Inventor
Frank Arthur Forward
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.)
Viridian Inc Canada
Original Assignee
Sherritt Gordon Mines Ltd
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
Priority to US65798A priority Critical patent/US2616781A/en
Priority to FR1071061D priority patent/FR1071061A/en
Application filed by Sherritt Gordon Mines Ltd filed Critical Sherritt Gordon Mines Ltd
Priority to GB1920252A priority patent/GB715243A/en
Publication of GB715243A publication Critical patent/GB715243A/en
Expired legal-status Critical Current

Links

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
    • C22B23/00Obtaining nickel or cobalt
    • C22B23/04Obtaining nickel or cobalt by wet processes
    • C22B23/0407Leaching processes
    • C22B23/0446Leaching processes with an ammoniacal liquor or with a hydroxide of an alkali or alkaline-earth metal

Landscapes

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

Abstract

Nickel values are extracted from material containing metallic nickel in a process comprising the steps (1) digesting the nickeliferous material without dissolving any appreciable amount of nickel values with an ammonia-ammonium carbonate solution (e.g. 8 per cent. ammonia, 8 per cent. ammonium carbonate) in the ratio by weight of about one part solids to about three parts solution, feeding an oxygen-bearing oxidizing gas into the mixture during the digesting step, continuing the digesting step until any reduced iron present is converted into an insoluble hydroxide, (2) leaching the digested mixture by dispersing it in a substantially larger volume of ammonia-ammonium carbonate solution sufficient to effect the leaching operation, agitating the mixture and feeding an oxygen-bearing oxidizing gas thereinto until at least the major portion of the metallic nickel values dissolve (3) separating the solids from the leach solution and (4) recovering the nickel values from the leach solution. Sulphide ores such as pentlandite may be first roasted under oxidizing conditions commencing at 500 DEG C. and progressively heated to 700-800 DEG C., and the so-formed oxide (or an oxide ore if this is used as the starting material) roasted under reducing conditions at a temperature of 400-600 DEG C. (better 480-525 DEG C. preferably in an atmosphere of hydrogen and with the use of a solid fuel, e.g. coke. If copper is present in sufficient quantity in the ore it may be removed after the oxidation with dilute sulphuric acid, and magnesium sulphate if present should be removed at the same stage by water washing. The flow sheet (not shown) indicates an embodiment in which a copper-containing sulphide ore is used. It is preferred to agitate the mixture mildly in the digesting step so that the solids are held in suspension and their mutual contacts effect a gently abrasive action. In the digesting step a temperature of 20-70 DEG C. is preferred and in the leaching step a two-stage modification of which is described, a superatmospheric temperature and pressure and a solids concentration of 5 per cent. by weight is preferable. It is stated that cobalt if present behaves in the same way as the nickel.ALSO:A starting material containing metallic nickel may be produced from oxidic materials such as oxide ores or oxidized sulphide ores, preferably in admixture with a solid reducing agent, e.g. coke. The reduction is preferably performed in an atmosphere of hydrogen at 400-600 DEG C. (better 480-525 DEG C.). According to the invention such material is used for extraction of nickel as carbonate by means of ammonia-ammonium carbonate solutions (see Group III). Cobalt if present is said to behave in the same way as nickel.
GB1920252A 1948-12-17 1952-07-30 Nickel process Expired GB715243A (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
US65798A US2616781A (en) 1948-12-17 1948-12-17 Treatment of nickeliferous oxide concentrates for recovery of nickel values therefrom
FR1071061D FR1071061A (en) 1952-07-30 1952-07-25 Treatment of nickel-containing materials
GB1920252A GB715243A (en) 1952-07-30 1952-07-30 Nickel process

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1920252A GB715243A (en) 1952-07-30 1952-07-30 Nickel process

Publications (1)

Publication Number Publication Date
GB715243A true GB715243A (en) 1954-09-08

Family

ID=10125441

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1920252A Expired GB715243A (en) 1948-12-17 1952-07-30 Nickel process

Country Status (2)

Country Link
FR (1) FR1071061A (en)
GB (1) GB715243A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009009825A1 (en) * 2007-07-13 2009-01-22 Metaleach Limited Method for ammoniacal leaching

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111408385B (en) * 2020-03-13 2024-03-22 吉林大学 Fe (Fe) 5 Ni 4 S 8 Preparation method of hydrogen evolution electrocatalytic material

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009009825A1 (en) * 2007-07-13 2009-01-22 Metaleach Limited Method for ammoniacal leaching
AU2011200703B2 (en) * 2007-07-13 2011-09-22 CAPSA Metals Pty Ltd Method for Leaching of a Copper-containing Ore
AU2008278269B2 (en) * 2007-07-13 2013-01-17 CAPSA Metals Pty Ltd Method for ammoniacal leaching
US8388729B2 (en) 2007-07-13 2013-03-05 Metaleach Limited Method for ammoniacal leaching
AP2742A (en) * 2007-07-13 2013-09-30 Metaleach Ltd Method for ammoniacal leaching

Also Published As

Publication number Publication date
FR1071061A (en) 1954-08-24

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