US1050630A - Art of separating copper from other metals. - Google Patents
Art of separating copper from other metals. Download PDFInfo
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- US1050630A US1050630A US62799311A US1911627993A US1050630A US 1050630 A US1050630 A US 1050630A US 62799311 A US62799311 A US 62799311A US 1911627993 A US1911627993 A US 1911627993A US 1050630 A US1050630 A US 1050630A
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- copper
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- reducible
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- 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
- C22B23/043—Sulfurated acids or salts thereof
Definitions
- My present invention relates generally to an improved process for separating copper from another metal or metals associated therewith, by dissolving out the copper and leaving the'other metal or metals unaifected.
- my invention relates tov an improved process for separating copper and nickel which are associated together in their metallic states by, dissolving out the copper and leaving the nickel unaffected.
- My improved process is particularly adapted to the manufacture of films or flakes of metallic nickel for use in themak" up of the positive-electrodes of storage batteries of the Edison type.
- the nlckel flake collects at the bottom of the solutlon, and the solution, together with the suspended ba'sic sulfate may be poured or $1- phoned 01f.
- the basic sulfate is then sep arated from the solution by subsidence or filtration.
- reaction I which takes of a reducible chlorid or ferric bromid, but these salts are more costly than the chlorids.
- the solution can be used continuously by filtering off the basic salt and adding a quantity of copper sulfate corresponding to the amount of sulfate removed from the basic salt.
- the cupric chlorid is regenerated during the reaction and remains in the liquid, it is only necessary to add a little from time to time to replace what is lost in the operation of filtermg.
- My improved process has the following advantages over the process described and claimed in my application Serial No. 626,298, filed May 9th, 1911:-First: The solution of the metallic copper is accomplished more rapidly than by using ammonium sulfate andcupric chlorid. Second: My improved nrocess is cheaper because in the process described in my prior application, ammonium sulfate must be supplied, whereas, in my improved process, sulfuric acid, which is cheaper than ammonium sulfate, is used. Third: The basic copper sulfate is more completely insoluble in the solution described in this application than in that described in my prior application, apparently because of the entire absence of ammonia and compounds of ammonia.
- My improved process is applicable generally to the separation of copper from such other metals as are not affected by the treatment hereinbefore described.
- copper from metallic nickel associated therewith which consists in treatingthe associated metals with a solution of copper sulfate containin a reducible haloid, and simultaneously stlrring, heating, and supplying oxygen containing gas to the mixture, substantially as described.
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- Chemical & Material Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Manufacture And Refinement Of Metals (AREA)
- Electrolytic Production Of Metals (AREA)
Description
UNITED STATES {PATENT OFFICE.-
THOMAS A. EDISON, or LLEWELLYN PARKQWEST ORANGE, NEW JERSEY.
ART OF SEPARATIN G COPPER FROM OTHER METALS.
No Drawing.
In Letters Patent of the United States No. 936,525, dated October 12, 1909, and Nos. 865,687 and 865,688, dated September 10, 1907, I have described processes for making metallic films or flakes, and particularly films or flakes of metallic nickel for use in the makeup of the positive electrodes of storage batteries of the Edison type. These processes consist generally'in forming composite sheets composed 'of alternating layers of electrolytically deposited copper and nickel, cutting up the sheets into strips or other small portions, and dissolving out the copper. In the hereinbefore mentioned Patent No. 865,687, I have described the use of an ammoniacal copper sulfate solution for dissolving the copper without affecting I the nickel, and in my application Serial No.
026,298, filed May 9th, 1911,. I have de-' scribed and claimed a method for accomplishing this result, in which I treat the associated metals with a solution of ammonium sulfate containing a small quantity of a reducible haloid, such as cupric chlorid, and simultaneously stir, heat, and supply air to the mixture.
My present invention relates generally to an improved process for separating copper from another metal or metals associated therewith, by dissolving out the copper and leaving the'other metal or metals unaifected.
More specifically, my invention relates tov an improved process for separating copper and nickel which are associated together in their metallic states by, dissolving out the copper and leaving the nickel unaffected.
My improved process is particularly adapted to the manufacture of films or flakes of metallic nickel for use in themak" up of the positive-electrodes of storage batteries of the Edison type.
I have discovered thatvmetallic copper is dissolved by asolution of copper sulfate containing a small quantity of a reducible haloid, such as cupric chlorid; that the ra pidity of the dissolving action is increased Specification of Letters Patent.
Patented Jan. 14, 1913;
Application filed May 18, 1911. Serial No. 627,993.
very. considerably by stirring and heating; that the reducible ehlorid'may be regenerated by supplying the solution with air,
oxygen, or other oxygen containing gas, and
the operation thereby rendered continuous without the necessity of adding additional quantities of reducible chlorid; and that the by-product is a pure basic sulfate of copper which can be made into pure sulfate of copper by adding the proper amount of sulfuric acid.
In the practice of my invention as applied to the manufacture of films or flakes of metallic nickel, I proceed substantially as follows:-Composite sheets each composed of a thin layer of copper and a thin layer of nickel, or of a number of such layers with copper and nickel alternating, are prepared by any of the methods described in the hereinbefore mentioned patents, or in any other suitable manner. Each of these sheets is then cut into strips or into small portions corresponding to the size of the flake desired, in the manner described in any of the hereinbefore mentioned patents. These strips or other small portions, each consisting of copper and nickel associated together in their metallic states, are then put into a solution of copper sulfate containing a small quantity other haloid, such as cupric chlorid. I have found that excellent results are obtained by using a 25% solution of sulfate of copper and about 15 grams of cupric -chlorid per liter of solution. These proportions may be varied within certain limits. The solution is preferably kept near the boiling point, and air blown into it from any suitable source, such as an air compressor. The air itself may be heated before being blown into the solution. The solution is also stirred, and the stirring may be accomplished by any suitable stirrlng apparatus, such as rotating vanes, or by the air forced in, or by both. As a result of'the reaction, the copper is separated out as a basic sulfate of copper, which is msoluble in the solution used, and which is held in suspension during the stirring. The nlckel flake collects at the bottom of the solutlon, and the solution, together with the suspended ba'sic sulfate may be poured or $1- phoned 01f. The basic sulfate is then sep arated from the solution by subsidence or filtration. In the reaction I which takes of a reducible chlorid or ferric bromid, but these salts are more costly than the chlorids.
In the process employed heretofore, in which the copper is dissolved in an ammoniacal solution of copper sulfate, it is necessary to use a large quantitypf free ammonia. The ammonia is expenslve, and even though it may be recovered afterward from the solution, the process of recovering it requires complicated apparatus and is eX- pensive. The operation of dissolving the copper in the ammoniacal solution must be carried on where air can reach the solution to insure the dissolving of the copper. As a result, the solution cannot be heated to hasten the reaction, because, if heated, too much ammonia would be driven off. Even when carried on without heating, fumes of ammonia are given off, which fill the building and produce disagreeable and irritating efi'ects. Furthermore, in this process, the copper is converted into a soluble salt, and its recovery in a useful form is expensive. In my improved process, ammonia and compounds of ammonia are entirely absent, and the copper is automatically thrown out as an insoluble compound, that is, as a basic copper sulfate which is practically pure and free from undesirable salts of ammonia, and whichcan be readily converted into copper sulfate by adding sulfuric acid. The copper sulfate ugly be used in the further practice of this process, or for any other purpose. Furthermore, the solution can be used continuously by filtering off the basic salt and adding a quantity of copper sulfate corresponding to the amount of sulfate removed from the basic salt. As the cupric chlorid is regenerated during the reaction and remains in the liquid, it is only necessary to add a little from time to time to replace what is lost in the operation of filtermg.
My improved process has the following advantages over the process described and claimed in my application Serial No. 626,298, filed May 9th, 1911:-First: The solution of the metallic copper is accomplished more rapidly than by using ammonium sulfate andcupric chlorid. Second: My improved nrocess is cheaper because in the process described in my prior application, ammonium sulfate must be supplied, whereas, in my improved process, sulfuric acid, which is cheaper than ammonium sulfate, is used. Third: The basic copper sulfate is more completely insoluble in the solution described in this application than in that described in my prior application, apparently because of the entire absence of ammonia and compounds of ammonia.
My improved process is applicable generally to the separation of copper from such other metals as are not affected by the treatment hereinbefore described.
Having now described my invention, what I claim as new and desire to protect by Letters Patent is as follows 1. 'The process of separating metallic copper from another metal or metals associated therewith, which consists in treating the associated metals with a solution of copper sulfate containing a reducible haloid of a metal of variable valence, substantially as described.
2. The process of separating metallic copper from another metal or metals associated therewith, which consists in treating the associated metals with a solution of copper sulfate containing a reducible haloid of a metal of variable valence, and heating the mixture, substantially as described.
3. The process of separating metallic copper from another metal or metals associated therewith, which consists in treating the associated metals with a solution of copper sulfate containing a reducible haloid of a metal of variable valence, and stirring the mixture, substantially as described.
4:. The process of separating metallic copper from another metal or metals associated therewith, which consists in treating the associated metals with a solution of copper sulfate containing a reducible haloid of a metal of variable valence, and heating and stirring the mixture, substantially as described.
5. The process of separating metallic copper from another metal or metals associated therewith, which consists in treating the associated metals with a solution of cop er sulfate containing a reducible haloid of a metal of variable valence, and supplying oxygen containing gas to the mixture, substantially as described.
6. The process of separating metallic copper from another metal or metals associated therewith, which consists in treating the associated metals with a solution of copper sulfate containing a reducible haloid of a metal of variable valence, heating the mixture and supplying oxygen containing gas thereto, substantially as described.
7. The process of separating metallic copper from another metal or metals associated therewith, which consists in treating the associated metals with a solution of copper sulfate containing a reducible haloid of a metal of variable valence, and simultaneously stirring, heating, and. supplying oxygen containing gas to the mixture, substantially as described.
8. The process of separating metallic copper from metallic nickel associated therewith, which consists in treating the associated metals with a solution of copper sulfate containing a reducible haloid, substantially as described.
9. The process of separating metallic copper from metallic nickel associated therewith, which consists in treating the associated metals with a solution of copper sulfate containing a reducible haloid, and heating the mixture, substantially as described.
10. The process of separating metallic copper from metallic nickel associated therewith, which consists in treating the associated metals with a solution of cop er sulfate containing a reducible haloid, and stirring the mixture, substantially as 'described.
11. The process of separating metallic copper from metallic nickel associated therewith, which consists in treating the associated metals with a solution of copper sulfate containing a reducible haloid, and heating and stirring the mixture, substantially as described.- v
12. The process of separating metallic copper from metallic nickel associated therewith, which consists in treating the associated metals with a solution of copper sulfate containing a reducible haloid, and supplying oxygen containing gas to the mixture, substantially as described.
13. The process of separating metallic copper from metallic nickel associated therewith, which consists in treating the associated metals with a solution of copper sulfate containing a reducible haloid, heating the mixture and supplying oxygen containing gas thereto, substantially as described.
14. The process of separating metallic,
copper from metallic nickel associated therewith, which consists in treatingthe associated metals with a solution of copper sulfate containin a reducible haloid, and simultaneously stlrring, heating, and supplying oxygen containing gas to the mixture, substantially as described.
15. The process of separating metallic copper from metallic nickel associated therewith, which consists in treating the associated metals with a solution of copper cupric chlorid, substancopper from metallic nickel associated therewith, which consists in treatin the associated metals with a solution 0 copper sulfate containing cupric chlorid, and heating and stirring the mixture, substantially as described.
19. The process of separating metallic copper from metallic nickel associated therewith, which consists in treating the associated metals with a solution of copper sulfate containing cupric chlorid, and supplying oxygen containing gas to the mixture, substantially as described.
20. The process of separating metallic copper from metallic nickel associated therewith, which consists in treating the associated metals with a solution of copper sulfate containing cupric chlorid, heating the mixture and supplyingoxygen containing gas thereto, substantially as described.
21. The process of separating metallic copper from -metallic nickel associated therewith, which consists in treat-ing the associated metals with a solution of copper sulfate containing cupric chlorid, and simultaneously stirring,-heating, and supplying oxygen, containing gas to the mixture, substantially as described.
22. The process of separating metallic copper from metallic nickel associated therewith, which consists in treatin the associated metals With a solution 0 copper sulfate containing cupric chlorid, stirring, 4
heating, and supplying air to the mixture, whereby the copper is converted into an insoluble salt, and then removing the said salt, substantially as describe This specification signed and witnessed this 12th day of May, 1911.
THOS. A. EDISON,
Witnesses HENRY LANAHAN, ANNA R. KLEHM.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US62799311A US1050630A (en) | 1911-05-18 | 1911-05-18 | Art of separating copper from other metals. |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US62799311A US1050630A (en) | 1911-05-18 | 1911-05-18 | Art of separating copper from other metals. |
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US1050630A true US1050630A (en) | 1913-01-14 |
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US62799311A Expired - Lifetime US1050630A (en) | 1911-05-18 | 1911-05-18 | Art of separating copper from other metals. |
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4039406A (en) * | 1973-08-10 | 1977-08-02 | Noranda Mines Limited | Recovering copper from concentrates with insoluble sulfate forming leach |
-
1911
- 1911-05-18 US US62799311A patent/US1050630A/en not_active Expired - Lifetime
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4039406A (en) * | 1973-08-10 | 1977-08-02 | Noranda Mines Limited | Recovering copper from concentrates with insoluble sulfate forming leach |
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