IL41674A - Recovery of copper,zinc or nickel from sulfide concentrates - Google Patents

Recovery of copper,zinc or nickel from sulfide concentrates

Info

Publication number
IL41674A
IL41674A IL41674A IL4167473A IL41674A IL 41674 A IL41674 A IL 41674A IL 41674 A IL41674 A IL 41674A IL 4167473 A IL4167473 A IL 4167473A IL 41674 A IL41674 A IL 41674A
Authority
IL
Israel
Prior art keywords
copper
concentrate
primary
process according
sulfide
Prior art date
Application number
IL41674A
Other versions
IL41674A0 (en
Original Assignee
Anaconda Co
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 Anaconda Co filed Critical Anaconda Co
Publication of IL41674A0 publication Critical patent/IL41674A0/en
Publication of IL41674A publication Critical patent/IL41674A/en

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
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B15/00Obtaining copper
    • C22B15/0063Hydrometallurgy
    • C22B15/0065Leaching or slurrying
    • C22B15/0078Leaching or slurrying with ammoniacal solutions, e.g. ammonium hydroxide
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B15/00Obtaining copper
    • C22B15/0063Hydrometallurgy
    • C22B15/0084Treating solutions
    • C22B15/0089Treating solutions by chemical methods
    • C22B15/0093Treating solutions by chemical methods by gases, e.g. hydrogen or hydrogen sulfide
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B19/00Obtaining zinc or zinc oxide
    • C22B19/20Obtaining zinc otherwise than by distilling
    • C22B19/24Obtaining zinc otherwise than by distilling with leaching with alkaline solutions, e.g. ammonia
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P10/00Technologies related to metal processing
    • Y02P10/20Recycling

Landscapes

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

Claims (12)

1. 41674/
2. WHAT WE CLAIM IS: A process for recovering copper, zinc or nickel from an ore containing such metal in the form of a sulfide mineral associated with iron sulfide, wherein the ore is treated by froth flotation to produce a primary sulfidic concentrate of said mineral together with associated iron sulfide, and leached with an aqueous solution conta4ning ammonium sulfate and free ammonia at a temperature in the range from 50°C. to 80°C. and at a pressure not exceeding 10 psig. in the presence of free oxygen, and the resultant pregnant leach solution is separated from the residual leached primary concentrates, characterized in that the leaching operation is terminated while a substantial amount*of undissolved copper, nickel or zinc remains in the residual leached primary concentrates, and said residual leached primary concentrates are subjected to a . flotation concentration operation .0 produce a secondary secondary/ concentrate substantially smaller in amount than the primary concentrate and to reject in the tailings of said secondary flotation operation iron sulfide of the primary concentrates which has been freed by the leaching operation from copper, nickel and zinc minerals. .- The process of claim 1 wherein the leaching operation is carried out y- vigorously agitating a slurry of the primary concentrates in the ammoniacal leach solution, characterized in that oxygen-bearing gas is continously recirculated throughout the leaching operation from above the surface of said slurry to a substantial depth below such surface. ·· ; ' ■ t 3.- The process of .either
3. The process according to claim 2 wherein the wash liquor from the washing operation is united with the leach solution for treatment to recover the dissolved metal .
4. A process according to any of the preceding claims wherein the undissolved solids after being separated from the leach solution and prior to the secondary flotation operation are subjected to releaching by being reslurried in aqueous ammonia-ammonium sulfate solution and by being vigorousl agitated in such slurry at a temperature from 60°C. to 90°C. and at a pressure not exceeding 10 psig. while vigorously recirculating free oxygen from above the surface of the slurry to a substantial depth below such surface.
5. The process according to any of the preceding . claims wherein the secondary sulfide concentrate is formed into a slurry in aqueous ammonia-ammonium sulfate solution and is releached by vigrjoously agitating such slurry at a temperature from 60°C. to 90°C. and at a pressure not exceeding 10 psig, while vigorously recirculating free oxygen from above the surface of the slurry to a substantial depth below such surface.
6. The process according to any of claims 1 to 4 wherein the secondary sulfide concentrate is smelted to recover its metal values.
7. The process according to any of the preceding claims in which the primary concentrate is a copper concentrate and contains in addition to copper other metal sulfide values > the primary concentrate, and said secondary concentrate is treated for the recovery of said other metal sulfide values.
8. The process according to claim 7, in which the primary concentrate contains a high proportion of copper sulfide minerals and a low proportion of molybdenite, wherein most of the copper sulfide minerals are dissolved in the course of the leaching operation, and substantially all the molybdenite is recovered in the secondary concentrate.
9. The process according to any of the preceding claims wherein primary concentrate is a copper concentrate and the aqueous leach solution is treated by a liquid ion exchanger dissolved in a liquid organic medium to extract the copper into the organic medium and to form an aqueous substantially copper-free raffinate containing ammonia and ammonium sulfate, the copper-loaded organic medium is treated with an aqueous sulfuric acid solution to recover the copper in the form of an acid copper sulfate solution and to regenerate the liquid ion exchanger, the raffinate is recycled for reuse in the leaching operations, and copper is electrowon from the acid copper sulfate solution.
10. The process according to claim 9 in which the primary concentrate contains zinc in addition to copper, and said zinc is dissolved in the leach solution and remains in the raffinate after liquid ion extraction of the copper, wherein at least a portion of the raffinate is treated to precipitate zinc as an insoluble compound therefrom, the precipitated zinc compound is separated from the residual solution, and the residual solution is treated for recovery of
11. The process according to claim 10 wherein at least a portion of the raffinate is treated with carbon dioxide under pressure to precipitate zinc in the form of an insoluble carbonate compound.
12. The process according to any of the preceding claims wherein the primary concentrate is a copper concentrate which comprises a substantial proportion of pyrite particles superficially coated with a copper sulfide mineral, such coating is dissolved in the leaching operation, and the resulting pyrite particles freed of such cupriferous coating are largely rejected in the tailings of the seconda COHEN ZEDEK & SPISBACH P.0. Box 33116 , Tel-Aviv Attorneys for Applicant
IL41674A 1972-03-07 1973-03-02 Recovery of copper,zinc or nickel from sulfide concentrates IL41674A (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US23245472A 1972-03-07 1972-03-07
US24234072A 1972-04-10 1972-04-10
US26570972A 1972-06-23 1972-06-23
US30147572A 1972-10-27 1972-10-27

Publications (2)

Publication Number Publication Date
IL41674A0 IL41674A0 (en) 1973-05-31
IL41674A true IL41674A (en) 1976-07-30

Family

ID=27499650

Family Applications (1)

Application Number Title Priority Date Filing Date
IL41674A IL41674A (en) 1972-03-07 1973-03-02 Recovery of copper,zinc or nickel from sulfide concentrates

Country Status (21)

Country Link
JP (1) JPS5438561B2 (en)
AR (1) AR203454A1 (en)
AU (1) AU472980B2 (en)
BE (1) BE796324A (en)
CA (1) CA998840A (en)
DE (1) DE2311242C3 (en)
FI (1) FI58347C (en)
FR (1) FR2175074B1 (en)
GB (1) GB1404244A (en)
IE (1) IE37546B1 (en)
IL (1) IL41674A (en)
IN (2) IN138729B (en)
IT (1) IT980494B (en)
NL (1) NL7303112A (en)
NO (1) NO133812C (en)
PH (1) PH11968A (en)
RO (1) RO64661A (en)
SE (1) SE397204B (en)
TR (1) TR17677A (en)
YU (1) YU59473A (en)
ZM (1) ZM4073A1 (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1490813A (en) * 1975-07-21 1977-11-02 Isc Smelting Leaching of copper dross
ZA766304B (en) * 1975-11-03 1977-09-28 Fluor Utah Flotation process
ES476055A1 (en) * 1978-12-15 1979-11-01 Redondo Abad Angel Luis Process for non-ferrous metals production from complex sulphide ores containing copper, lead, zinc, silver and/or gold
EP0030067A1 (en) * 1979-11-30 1981-06-10 The Board Of Trustees Of The Michigan State University Process for the extraction of metal ions
SE446276B (en) * 1980-11-17 1986-08-25 Boliden Ab PROCEDURE FOR Separating and Extracting Nickel and Copper from Complex Sulfide Minerals
US11286540B2 (en) * 2020-07-31 2022-03-29 Rio Tinto Technological Resources Inc. Method of processing a pyrite-containing slurry

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2576314A (en) * 1948-11-06 1951-11-27 Sherritt Gordon Mines Ltd Extracting of nickel values from nickeliferous sulfide material
BE514331A (en) * 1951-09-21 1900-01-01
US2822263A (en) * 1954-09-01 1958-02-04 Sherritt Gordon Mines Ltd Method of extracting copper values from copper bearing mineral sulphides
DE1051511B (en) * 1954-09-21 1959-02-26 Sherritt Gordon Mines Ltd Process for the extraction of copper from sulphidic copper ores
US2912305A (en) * 1956-05-31 1959-11-10 Metals And Chemicals Corp Non-ferrous scrap treatment
US3582314A (en) * 1967-02-10 1971-06-01 Ihara Chemical Co Method for killing grassy and broadleaf weeds

Also Published As

Publication number Publication date
AU5283573A (en) 1974-09-05
AR203454A1 (en) 1975-09-15
IN139440B (en) 1976-06-19
DE2311242C3 (en) 1982-02-25
FR2175074B1 (en) 1977-08-12
FR2175074A1 (en) 1973-10-19
NO133812B (en) 1976-03-22
AU472980B2 (en) 1976-06-10
NL7303112A (en) 1973-09-11
IT980494B (en) 1974-09-30
RO64661A (en) 1979-02-15
JPS5438561B2 (en) 1979-11-21
BE796324A (en) 1973-09-06
JPS4974601A (en) 1974-07-18
DE2311242A1 (en) 1973-09-13
GB1404244A (en) 1975-08-28
IE37546B1 (en) 1977-08-17
TR17677A (en) 1975-07-23
NO133812C (en) 1976-06-30
FI58347C (en) 1981-01-12
ZM4073A1 (en) 1974-11-21
FI58347B (en) 1980-09-30
PH11968A (en) 1978-09-28
IE37546L (en) 1973-09-07
CA998840A (en) 1976-10-26
IN138729B (en) 1976-03-20
DE2311242B2 (en) 1981-06-25
SE397204B (en) 1977-10-24
YU59473A (en) 1982-02-28
IL41674A0 (en) 1973-05-31

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