US1375631A - Process of separating and refining metals - Google Patents
Process of separating and refining metals Download PDFInfo
- Publication number
- US1375631A US1375631A US265383A US26538318A US1375631A US 1375631 A US1375631 A US 1375631A US 265383 A US265383 A US 265383A US 26538318 A US26538318 A US 26538318A US 1375631 A US1375631 A US 1375631A
- Authority
- US
- United States
- Prior art keywords
- solution
- copper
- nickel
- metal
- granules
- 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 - Lifetime
Links
- 239000002184 metal Substances 0.000 title description 40
- 229910052751 metal Inorganic materials 0.000 title description 40
- 238000000034 method Methods 0.000 title description 17
- 230000008569 process Effects 0.000 title description 15
- 150000002739 metals Chemical class 0.000 title description 12
- 238000007670 refining Methods 0.000 title description 10
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 59
- 239000010949 copper Substances 0.000 description 41
- 229910052802 copper Inorganic materials 0.000 description 38
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 36
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 30
- 229910052759 nickel Inorganic materials 0.000 description 28
- 239000008187 granular material Substances 0.000 description 22
- 239000002253 acid Substances 0.000 description 16
- 230000007935 neutral effect Effects 0.000 description 12
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 11
- 239000000463 material Substances 0.000 description 9
- 238000004090 dissolution Methods 0.000 description 7
- 229910000570 Cupronickel Inorganic materials 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 239000004568 cement Substances 0.000 description 4
- YOCUPQPZWBBYIX-UHFFFAOYSA-N copper nickel Chemical compound [Ni].[Cu] YOCUPQPZWBBYIX-UHFFFAOYSA-N 0.000 description 4
- 238000005868 electrolysis reaction Methods 0.000 description 4
- 230000003472 neutralizing effect Effects 0.000 description 4
- 230000009471 action Effects 0.000 description 3
- LGQLOGILCSXPEA-UHFFFAOYSA-L nickel sulfate Chemical compound [Ni+2].[O-]S([O-])(=O)=O LGQLOGILCSXPEA-UHFFFAOYSA-L 0.000 description 3
- 229910000363 nickel(II) sulfate Inorganic materials 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 238000003723 Smelting Methods 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- TVZPLCNGKSPOJA-UHFFFAOYSA-N copper zinc Chemical compound [Cu].[Zn] TVZPLCNGKSPOJA-UHFFFAOYSA-N 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 150000002736 metal compounds Chemical class 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- 238000010306 acid treatment Methods 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 150000001879 copper Chemical class 0.000 description 1
- 229910000365 copper sulfate Inorganic materials 0.000 description 1
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 1
- 108010082357 dividin Proteins 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 1
- 230000002101 lytic effect Effects 0.000 description 1
- -1 magnetite Chemical compound 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000011946 reduction process Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B23/00—Obtaining nickel or cobalt
- C22B23/04—Obtaining nickel or cobalt by wet processes
- C22B23/0407—Leaching processes
- C22B23/0415—Leaching processes with acids or salt solutions except ammonium salts solutions
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B15/00—Obtaining copper
- C22B15/0063—Hydrometallurgy
- C22B15/0065—Leaching or slurrying
- C22B15/0067—Leaching or slurrying with acids or salts thereof
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B15/00—Obtaining copper
- C22B15/0063—Hydrometallurgy
- C22B15/0084—Treating solutions
- C22B15/0089—Treating solutions by chemical methods
- C22B15/0091—Treating solutions by chemical methods by cementation
-
- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P10/00—Technologies related to metal processing
- Y02P10/20—Recycling
Definitions
- This inventiton relates to the treatment of alloys or metal compounds such as are obtained by smelting of complex ores like copper-nickel ores and copper-zinc ores.
- the object of the invention is amethod whereby the metals contained in such alloys or metal 'compounds may be recovered separately and in a practically pure condition.
- My process may be used for the treatment of various metal compounds, but I have found that it is especially suitable for the treatment of copper-nickel materials such as the matte obtained from the smelting of copper-nickel ores.
- Sulfuric acid is generally the most suitable acid for this purpose but other acids capable of dissolving copper and nickel may be used. -In the following description of my process I will however for convenience only refer to sulfuric ⁇ acid.
- air is introduced at the same time as the acid which is periodically passed through the mass of granules.
- the acid used as a solvent will be neutralized and if sulfuric acid is used there will result a neutral solution containing principally copper sulfate and nicket sulfate.
- the anode compartments are furnished with inlets and outlets for the anolyte and may be connected in such al manner that the solution may pass through one anode compartment after the other.
- the cathode compartments are connected in slmilar manner.
- the contents of acid of the anolyte can be regulated and raised to the desired amount by regulating and reducing the speed of the solution passing through the anode compartments
- the circulation of the catholyte may be arranged so as to give the best conditions for a smooth deposit of nickel on the cathode.
- the acid solution leaving the anode-comp artments is led to the towers for dissolution of granules.
- the solution is agam neutralized and freed from copper. whereupon it is returned to the electro-l lytic vats.
- granules contain approximately 60% Ni and 40% Cu including small amounts of 1mpurities.
- a which may be of any suitable construction the acid solution coming from the anode compartments, d, is periodically percolating until all acid 1s neutralized and further until the nickel of the granules has plated out all copper from the solution.
- the neutralized solution will contaln approximate'ly 24 g. Ni and 16 g. Cu per liter, and finally after the Cu has been plated out a neutral solution will result containing 40 g. Ni per liter and being practically free from impurities.
- This solution is pumped into the vat, I), in which it is mixed with the solution from the vat, f, which runs into the vat, b, through the pipe, g.
- the solution from the vat, 7, has ⁇ just passed through the cathode compartments, c, in which apart of its Ni has been plated out.
- From the vat, b the solution runs into. the cathode compartments, 0, of the electrolytic cells in which a suitable circulation is provided according to known methods.
- a small portion of the cathode solution in the vat, f is led by means of pipe e into the anode compartments, d, which are separated from the cathode compartments .by means of the diaphragms, it.
- sulfuric acid is formed at the anode, and the solution will when leaving the anode compartments be comparatively rich in sulfuric acid. It is then returned to the towers, a, for dissolution of granules as above described.
- the electrolytic cells are of the type generally used for such purposes, the cathodes preferably being made of sheet iron and the anodes being made of a material which will not dissolve or disintegrate under the action of sulfuric acid and oxygen, such as magnetite, hard lead and others.
- Several cells may be connected inseries, each cell re- -quiring a voltage of about 3.2 volts when a. current density of 10-15 amperes per square foot is used. Under these conditions aV current efiiciency of about 90-95% is obtained and the nickel deposited on the cathodes runs 99% Ni or more.
- the cement copper which accumulates in ,the towers for cementation is vfrom time to time removed' and discarded from the process.'
- the process of separating and refining metals comprising the steps of treating granules containing copper and another metal with sulfuric acid solution, whereb copper and the other metal are dissolve thereby neutralizing the sulfuric acid solution, continuing the treatment after the solution has become neutral, wherebyA copper is cemented outby the other metal and a pure sulfate solution of said metal is formed, electrolyzing said sulfate solution in a diaphragm cell leading the solution first throu h the cathode compartment of the cell, wereby metal is deposited on the cathode, then dividin the solution in two fed throu h the anode compartment and the other eing mixed with the solution entering the cathode compartment, and using the solution leaving the anode compartment, rich in sulfuric acid, for dissolution of new amounts of granules containing copper and another metal.
- the process of separating and refining metals comprising the steps of treating granules containing copper and nicked with sulfuric acid solution whereby copper and nickel are dissolved thereby neutralizing the sulfuricr acid solution, continuing the treatment after the solution has become l.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Electrolytic Production Of Metals (AREA)
Description
G. HAGLUND. PROCESS 0F SEPARATING AND REFINING METALS.
' APPLICATION FILED Dc.5,19|s.
1,375,631 Patented Apr. 19, 1921.
Inventor, Gus'taf Haglund UNITED STATES PAT-ENT OFFICE.
GUSTAF HAGLUND, 0F FALUN, SWEDEN.
Specification of Letters Patent.
Patented Apr. 19, 1921.
Application inegi December's, 191s. serial No. 265,383.
To all 'whom 'it may concern.'
Be it known that I, GUs'rAF I-IAGLUND, a subject of Sweden, and a resident of Falun, Kingdom of Sweden, have invented certain new and useful Improvements in Processes of Separating and Refining Metals, of which the following is a specification.
This inventiton relates to the treatment of alloys or metal compounds such as are obtained by smelting of complex ores like copper-nickel ores and copper-zinc ores.
The object of the invention is amethod whereby the metals contained in such alloys or metal 'compounds may be recovered separately and in a practically pure condition. l
My process may be used for the treatment of various metal compounds, but I have found that it is especially suitable for the treatment of copper-nickel materials such as the matte obtained from the smelting of copper-nickel ores.
In order to recover the metals contained in such matte according to my invention I first subject the matte to a roasting and subsequent reduction process such 'as is well known and commonly practised, and granulate the resulting product which principally consists of metallic copper and nickel v These granules are brought into towers in which they are treated with an acid solu.
tion. Sulfuric acid is generally the most suitable acid for this purpose but other acids capable of dissolving copper and nickel may be used. -In the following description of my process I will however for convenience only refer to sulfuric `acid. During the treatment of the granules in the towers air is introduced at the same time as the acid which is periodically passed through the mass of granules. As the treatment progresses the acid used as a solvent will be neutralized and if sulfuric acid is used there will result a neutral solution containing principally copper sulfate and nicket sulfate. I have found that as long as the solution contains acid, both copper and nickel will enter into solution, the amount of each' metal dissolved being in proportion to the amount contained in the granules. But when the solution has become neutral a cementation process takes place, the nickel contained in the granules plating out the more electronegative copper. Thereafter only nickel will enter into solution, and an qpeivalent amount of copper will precipi- I can continue this treatment until a solution of nickel sulfate isobtainedwhich is free from copper. 0 I subject this solution to electrolysis using insoluble anodes, separated from'the cathodes by means of diagrams, whereby the nickel sulfate is decomposed, metallic nickel being deposited on the cathode and sulfuric acld belng formed at the anode.
I have found that this electrolytic process may advantageously be combined with above mentloned dissolution process, vthereby utillzlng the acid formed during yelectrolysls for the dissolution of granules.
I prefer to arrange several electrolytic vats each containing a plurality of anodes and cathodes. The anode compartments are furnished with inlets and outlets for the anolyte and may be connected in such al manner that the solution may pass through one anode compartment after the other.
The cathode compartments are connected in slmilar manner. By such arrangement of the two, independent systems of circulation I obtain great advantages. First, the contents of acid of the anolyte can be regulated and raised to the desired amount by regulating and reducing the speed of the solution passing through the anode compartments, second, the circulation of the catholyte may be arranged so as to give the best conditions for a smooth deposit of nickel on the cathode.
The acid solution leaving the anode-comp artments is led to the towers for dissolution of granules. By the treatment of the granules as above set forth the solution is agam neutralized and freed from copper. whereupon it is returned to the electro-l lytic vats.
In the tower or towers in which the 'cementation takes place a considerable amount of cement copper will collect. I remove this copper in any convenient manner and either sell it as cement copper or sub- ]ect 1t`to a refining process according to known methods. 'i
In the diagram forming part of this application is shown the arrangement of the various apparatus by means of which my invention is carried out. In the specific example chosen for illustrationpa. designates three towers lilled with granules. The
granules contain approximately 60% Ni and 40% Cu including small amounts of 1mpurities.
In the towers, a, which may be of any suitable construction the acid solution coming from the anode compartments, d, is periodically percolating until all acid 1s neutralized and further until the nickel of the granules has plated out all copper from the solution. Thus if the solution coming. from the anode compartments, d, contains about 15 g. Ni per liter and 40 g. HZSO,1 per liter the neutralized solution will contaln approximate'ly 24 g. Ni and 16 g. Cu per liter, and finally after the Cu has been plated out a neutral solution will result containing 40 g. Ni per liter and being practically free from impurities. This solution is pumped into the vat, I), in which it is mixed with the solution from the vat, f, which runs into the vat, b, through the pipe, g. The solution from the vat, 7, has `just passed through the cathode compartments, c, in which apart of its Ni has been plated out. From the vat, b, the solution runs into. the cathode compartments, 0, of the electrolytic cells in which a suitable circulation is provided according to known methods. A small portion of the cathode solution in the vat, f, is led by means of pipe e into the anode compartments, d, which are separated from the cathode compartments .by means of the diaphragms, it. During electrolysis sulfuric acid is formed at the anode, and the solution will when leaving the anode compartments be comparatively rich in sulfuric acid. It is then returned to the towers, a, for dissolution of granules as above described.
The electrolytic cells are of the type generally used for such purposes, the cathodes preferably being made of sheet iron and the anodes being made of a material which will not dissolve or disintegrate under the action of sulfuric acid and oxygen, such as magnetite, hard lead and others. Several cells may be connected inseries, each cell re- -quiring a voltage of about 3.2 volts when a. current density of 10-15 amperes per square foot is used. Under these conditions aV current efiiciency of about 90-95% is obtained and the nickel deposited on the cathodes runs 99% Ni or more. The cement copper which accumulates in ,the towers for cementation is vfrom time to time removed' and discarded from the process.'
Instead of using metallic granules in the towers, a, I may partly substitute these by granulated converter matte, as I have found that the sulfids may be dissolved upon formation of sulfates by the treatment in the towers as above described. Thus a great saving is obtained in the costs of roasting and reduction, as the metallic granules need only be used 1n such an amount as is required to cement out the Cu dissolved by the acid solution. The cementation will of course not be effected by suiids.
In the previous description I have only referred to copper-nickel materials. It is to be understood however that a similar result will be obtained when operating according to my methoden other materials such as copperzinc or others whose metals have an electrolytic relation to each other equal to that of copper and nickel.
It is further to be understood in referring in the claims hereof to the solution resulting from the acid treatment as being neutral, and to theV solution following the cementation step as being pure, that the terms are employed in the technical sense from an industrial standpoint and not in an absolute sense from the standpoint of the chemical laboratory.
The foregoing detailed description has been given for clearness of understanding, and no undue limitation should be deduced therefrom, but the appendedv claims should be construed as broadly as permissible in view'of the prior art. Y
What I claim as new and desire to secure byl Letters Patent of the United 'States is:
'1. In the separating and refining of metals the process of recovering copper and another metal from material in granular form containing the same, which comprises subjecting the said material to the action. of an acid solution whereby the copper and the other metal are dissolved and a neutral solution formed, continuing the treatment after the formation of the said solution until the copper is lcemented out by the other' metal and a pure solution of the last named -metal is formed, and recovering the said the said metal is deposited on the cathode in' refined condition.
2.` In the separating and refining of metals the processof recovering copper and another metal from material in granular form containing the same, which comprises subjecting the said material to the action of a sulfuric acid solution whereby the copper and the other metal are dissolved and a neutral solution formed, continuing the treatment after the formation of said solution until the copper is cemented out by the other metal and a pure sulfate solution of the'last named metal is formed, land recovering the said metal from the last named solution by subjecting the solution to electrolysis where by the said metal is deposited on the cathode in refined condition.
3. In the separating and refining of metals the process of recovering copper and nickel from material in granular form conv taining the same, which comprises subjectfurie acid solution whereby the copper and the nickel are dissolved and a neutral solution formed, continuing the treatment after the formation of the said solution until the copper is cemented out by the nickel and a pure solution of nickel sulfate is formed, and recovering the nickel from the last named solution by subjecting the solution to electrolysis whereby the nickel is deposited on the cathode in refined condition, 4. The process of separating and refining metals comprising the steps of treating granules containing copper and another metal with sulfuric acid solution, whereb copper and the other metal are dissolve thereby neutralizing the sulfuric acid solution, continuing the treatment after the solution has become neutral, wherebyA copper is cemented outby the other metal and a pure sulfate solution of said metal is formed, electrolyzing said sulfate solution in a diaphragm cell leading the solution first throu h the cathode compartment of the cell, wereby metal is deposited on the cathode, then dividin the solution in two fed throu h the anode compartment and the other eing mixed with the solution entering the cathode compartment, and using the solution leaving the anode compartment, rich in sulfuric acid, for dissolution of new amounts of granules containing copper and another metal.
5. The process of separating and refining metals comprising the steps of treating granules containing copper and nicked with sulfuric acid solution whereby copper and nickel are dissolved thereby neutralizing the sulfuricr acid solution, continuing the treatment after the solution has become l. through the anode compartment an neutral whereby copper is cemented out by the nickel and a pure sulfate solution of nickel is formed, electrolyzing said sulfate solution Ain a diaphra cell, leading the solution first through t e cathode compartment of the cell, whereby nickel is deposited on the cathode, then dividing the solution in two parts, one part bein lleld t e other being mixed with the solution entering the cathode compartment, and using the solution leaving the anode compartment metal in the form of su rich in sulfuric acid, for dissolution of new amounts ofgranules containing copper and ,is cemented .out by the other metal and a pure 'sulfate solution of said metal is formed and electrol zing said solution whereby the metal is eposited on the cathvode in a rened condition.
7. The process of separating and refining metals comprising the steps of treating granules containingcopper and nickel in the form of sulfids with a sulfuric acid so-.
lution whereby said sulfids are dissolved, thereby neutralizing the sulfuric acid solution, using the neutral solution forA treatment of ranules containing metallic 'copper and nickel, wherebyl copper is cemented out -by the nickel and a pure nickel sulfate4 .acid solution, using the neutral solution for treatment of granules containin metallic copper and another metal where y copper is cemented out by the other metal and a pure sulfate solution of said metal is formed, electrolyzing said sulfate solution in a diaphragm cell, leading the solution first through the cathode compartment of the cell whereby metal is deposited'on the cathode, then dividing the solution in two parts, one part bein led through the anode compartment and t e other being mixed with the solution entering the cathode compartment, and using the solution leaving the anode compartment, rich in sulfuric acid, for dissolution of new amounts of granules containing co er` and another metal in the form of su ds.
9. The process of se arating and refining metals comprising t e steps of treating granules containing copper and nickel in the form of sulids with a sulfuric acidsolution, whereby said sulids are dissolved, thereby neutralizing the sulfuric acid solution, using the neutral solution for v treatment of ranules containing metallic copper and nlckel whereby copper is cemented out by the nickel and a ure sulfate solution of nickel is formed, e ectrolyzing said sulfate solution in a diaphragm cel whereby nickel is de osited on the cathode,
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US265383A US1375631A (en) | 1918-12-05 | 1918-12-05 | Process of separating and refining metals |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US265383A US1375631A (en) | 1918-12-05 | 1918-12-05 | Process of separating and refining metals |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1375631A true US1375631A (en) | 1921-04-19 |
Family
ID=23010209
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US265383A Expired - Lifetime US1375631A (en) | 1918-12-05 | 1918-12-05 | Process of separating and refining metals |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1375631A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2480771A (en) * | 1946-04-12 | 1949-08-30 | Int Nickel Co | Process for the electrolytic recovery of nickel |
| US2595387A (en) * | 1942-12-05 | 1952-05-06 | Bolidens Gruv Ab | Method of electrolytically recovering nickel |
| US2603594A (en) * | 1947-05-13 | 1952-07-15 | Vanadium Corp Of America | Method of electrolytically producing manganese |
| US3969207A (en) * | 1975-03-05 | 1976-07-13 | Licencia Talalmanyokat Ertekesito Vallalat | Method for the cyclic electrochemical processing of sulfuric acid-containing pickle waste liquors |
-
1918
- 1918-12-05 US US265383A patent/US1375631A/en not_active Expired - Lifetime
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2595387A (en) * | 1942-12-05 | 1952-05-06 | Bolidens Gruv Ab | Method of electrolytically recovering nickel |
| US2480771A (en) * | 1946-04-12 | 1949-08-30 | Int Nickel Co | Process for the electrolytic recovery of nickel |
| US2603594A (en) * | 1947-05-13 | 1952-07-15 | Vanadium Corp Of America | Method of electrolytically producing manganese |
| US3969207A (en) * | 1975-03-05 | 1976-07-13 | Licencia Talalmanyokat Ertekesito Vallalat | Method for the cyclic electrochemical processing of sulfuric acid-containing pickle waste liquors |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4002544A (en) | Hydrometallurgical process for the recovery of valuable components from the anode slime produced in the electrolytical refining of copper | |
| NO149822B (en) | METAL ANODE FOR ELECTROLYCLE CELLS WITH Aqueous ELECTROLYTES AND PROCEDURES FOR PRODUCING THEREOF | |
| AU2011339119A1 (en) | Electrorecovery of gold and silver from thiosulphate solutions | |
| US5569370A (en) | Electrochemical system for recovery of metals from their compounds | |
| US1911604A (en) | Electrolytic process for the recovery of lead from waste materials | |
| US4030989A (en) | Electrowinning process | |
| US507130A (en) | Carl hoepfner | |
| US1375631A (en) | Process of separating and refining metals | |
| US1019969A (en) | Electrolysis of metallic solutions. | |
| RU2706400C9 (en) | Method of processing copper-nickel sulphide materials | |
| US2066347A (en) | Production of nickel by electrolytic deposition from nickel salt solutions | |
| CN113026056A (en) | Method for producing electrolytic cobalt by adopting secondary electrolysis of cobalt intermediate product | |
| US1844937A (en) | Process of electrolytic copper refining | |
| US2385269A (en) | Process of electrolytically extracting metal | |
| US669442A (en) | Process of recovering and separating metals by electrolysis. | |
| US1569137A (en) | Refining of copper-nickel matte | |
| US874496A (en) | Process of rendering soluble in water the nickel and copper contained in sulfid ores and mattes. | |
| US3054736A (en) | Method and apparatus for recovery of copper and zinc from scrap | |
| US3202593A (en) | Electrolytic precipitation of copper | |
| US2348742A (en) | Magnesium control in manganese electrowinning | |
| US1255439A (en) | Process of recovering zinc from ores. | |
| AU654774B2 (en) | Electrochemical system for recovery of metals from their compounds | |
| US830639A (en) | Process for the electrolytic production of copper. | |
| US1380711A (en) | Arthur e | |
| US592055A (en) | Process of treating ores |