US214344A - Improvement in separating metals by electrolysis - Google Patents
Improvement in separating metals by electrolysis Download PDFInfo
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- US214344A US214344A US214344DA US214344A US 214344 A US214344 A US 214344A US 214344D A US214344D A US 214344DA US 214344 A US214344 A US 214344A
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- solution
- metals
- anode
- cell
- copper
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- 239000002184 metal Substances 0.000 title description 54
- 229910052751 metal Inorganic materials 0.000 title description 54
- 150000002739 metals Chemical class 0.000 title description 42
- 238000005868 electrolysis reaction Methods 0.000 title description 10
- 239000000243 solution Substances 0.000 description 62
- RYGMFSIKBFXOCR-UHFFFAOYSA-N copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 38
- 229910052802 copper Inorganic materials 0.000 description 38
- 239000010949 copper Substances 0.000 description 38
- BQCADISMDOOEFD-UHFFFAOYSA-N silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 34
- 229910052709 silver Inorganic materials 0.000 description 34
- 239000004332 silver Substances 0.000 description 34
- 210000000188 Diaphragm Anatomy 0.000 description 26
- 229910045601 alloy Inorganic materials 0.000 description 24
- 239000000956 alloy Substances 0.000 description 24
- 229910001111 Fine metal Inorganic materials 0.000 description 18
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 18
- 229910052737 gold Inorganic materials 0.000 description 18
- 239000010931 gold Substances 0.000 description 18
- 239000010953 base metal Substances 0.000 description 14
- 238000007670 refining Methods 0.000 description 12
- 239000002253 acid Substances 0.000 description 10
- 238000000034 method Methods 0.000 description 10
- REDXJYDRNCIFBQ-UHFFFAOYSA-N aluminium(3+) Chemical class [Al+3] REDXJYDRNCIFBQ-UHFFFAOYSA-N 0.000 description 8
- 230000005611 electricity Effects 0.000 description 8
- 239000000463 material Substances 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- 239000002244 precipitate Substances 0.000 description 8
- 230000000694 effects Effects 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 230000001376 precipitating Effects 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- 239000012047 saturated solution Substances 0.000 description 4
- 239000011780 sodium chloride Substances 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-L sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 4
- 235000011149 sulphuric acid Nutrition 0.000 description 4
- 239000001117 sulphuric acid Substances 0.000 description 4
- 210000003165 Abomasum Anatomy 0.000 description 2
- 229910001316 Ag alloy Inorganic materials 0.000 description 2
- 229910001020 Au alloy Inorganic materials 0.000 description 2
- 229910000881 Cu alloy Inorganic materials 0.000 description 2
- 235000014676 Phragmites communis Nutrition 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 238000005266 casting Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000004020 conductor Substances 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 239000012528 membrane Substances 0.000 description 2
- 239000011259 mixed solution Substances 0.000 description 2
- -1 ore Substances 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25C—PROCESSES FOR THE ELECTROLYTIC PRODUCTION, RECOVERY OR REFINING OF METALS; APPARATUS THEREFOR
- C25C1/00—Electrolytic production, recovery or refining of metals by electrolysis of solutions
- C25C1/12—Electrolytic production, recovery or refining of metals by electrolysis of solutions of copper
Definitions
- This object I effect by subjecting anodes composed of the base alloys or metals to be operated upon to the action of an electrolytic bath which is a solvent of the coarser metal or metals present in the anode, and which is contained in two cells or compartments, one for the anode and the other for the cathode, separated from each other by a porous diaphragm which is impermeable to the undissolved fine metal or metals, and also impermeable to the precipitate of a fine metal which may have been dissolved, and which. by reason of its porosity, serves to electrically connect the two cells.
- My invention therefore, consists in the combination, in the same electrolytic bath, of the operations of decomposing an anode of base alloy by dissolving only the coarser metals present in the anode, and of separating the undissolved fine metal from the dissolved base metal present.
- composition of my electrolytic bath or solution will be varied according to the various metals which may be contained in the alloy which isto be refined, and that the size and form of the cells containing the solution may be determined at the will of the constructer, and with reference to the magnitude of the operations contemplated; my invention being present when a porous diaphragm, separating the cells and affording a path for the electric current, is employed to detain in the anodecell an undissolved fine metal, while one or more coarser metals which have been dissolved are removed from the anodecell.
- My anodes are formed by casting the alloy into ingots of suitable form and size, and I employ a copper cathode or cathodes whose combined area equals that of the anodes. With such a solution the copper contained in the anode is first dissolved, and the solution then dissolves the silver. When the silver and copper are both dissolved the gold falls to the bottom of the cell in the form of slime, being prevented from passing into the oath ode-cell by my porous diaphragm. I may remove the solution of copper and silver from the anode-cell and collect the gold slime therefrom; or I may precipitate the silver which has been dissolved, and remove only the copper solution.
- the precipitation of the silverI employ any of the known agents for this purpose, as, for example, the protoxide of iron.
- the removal from the anode-cell of the metals in solution may be effected by allowing them to pass through the porous diaphragm into the cathode-cell, or they may be remoyed by means of a pump or siphon.
- the silver is precipitated in the anode-cell I collect it, together wi h the gold slime, after the removal of the copper solution, and separate the silver precipitate from the gold slime by redissolving the silver, using for this purpose any of the known solvents of silver. I then have remaining the pure gold which was originally contained in the alloyed anode.
- Figure l is a vertical central section of an apparatus consisting of two cells, one above the other, separated hy two paral el diaphragms of porous material, establishing an intermediate chamber betwe n the cells.
- Figure l is a vertical central section of an apparatus consisting of two cells, one above the other, separated hy two paral el diaphragms of porous material, establishing an intermediate chamber betwe n the cells.
- Fig. 2 is a. top view of the upper cell
- Fig. 3 a plan of the lower cell.
- the apparatus represented in the drawings consists of the lower cell, A, which is a vat made of wood or other suitable material, and in which are suspended from a suitable frame the plates (1, that form the cathode. These plates are made of coppe plastic carbon, or other well-known material, according to the metal to be reduced.
- vat ll which is the anode-cell, in which the anodes b are suitably suspended.
- the frames of the anode and cathode are, respectively, connected with the opposite poles of a dynamo-electric machine or other source of electricity.
- the bottom of the anode-cell B is made of a diaphragm, ll, made of animal membrane orof porousclay, or some other material ⁇ v ich is impermeable to the undissolved metal, but sufliciently permeable to the solution to make it; a conductor of electricity, and thus ati'ord a free passage of the electric current from the solution in the anodecell to the solution in the cathodecell.
- the dissolved metals in the solution maybe separated from the undissolved metal by being allowed to pass through the diaphragm from the anode-cell into the cathode-cell, or they may be removed by a siphon or pump. 1n the latter case, as one diaphragm might not be suflicient to prevent the passage of the dissolved metals into the cathodecell, a third in termedlate vessel, C, is employed, the bottom of which is also a porous diaphragm, C.
- the intermediate space between the two d iaphragms is kept tilled with a constantly-running solution, that takes up and removes any of the solution which may have escaped from the anode-cell through the upper diaphram.
- the surface of the anode is made equal to the surfaceot' the cathode, so that, more or less, the same area is brought into action at both electrodes.
- the vats are provided with suitable rubber or other tubes, that supply the solutions or baths, and with siphous or outlet-pipes for re lnoving the same.
- the anode and cathode plates may be arranged either in vertical position or in horizontal, inclined, or other position.
- the dissolved metals may be drawn ofi' continuously from near the bottom of the anodecell. and fresh diluted acid added, as may be proportionately required.
- the solution containing the dissolved copper and silver is conducted, preferably by gravity, to a conveniently-placed trough of suitable length, which is filled, in part, with granulated copper, on which the silver will be precipitated.
- the remaining solution, thus t'reed from silver, is conducted into a lower vat. in which the copper is precipitated in the usual manner.
- the remaining tree acid is then drawn off into a still lower vat, and diluted preparatory to being again used in the anodecell,as at first.
- the top vat or anode-cell is supplied either with diluted acids or salts, according to the metals to be treated, and the liquid kept passing between thediaphragms is diluted acid or slightly acidulated water.
- the arrangement of the baths or solutions and of the anode and cathode, and the materials employed, may, of course, be altered according to the different metals.
- the apparatus may be worked with different solutions in thetop and bottom vats for dissolving one metal, ore, or combination in the acid solution of the top vat, While at the same time precipitating some other metal or salt from an ammoniacal or alkaline solution in the bottom vat.
- the process of refining and separating base alloys or base metals herein described which consists in subjecting such alloys as anodes to the electrolytic action of a solution which is a solvent of the coarser metals present, and in preventing the escape of the undissolved fine metals into the cathode-cell by interposing between the anode and cathode cells a porous diaphragm impermeable except to the metals in solution, and in removing the dissolved metals from the anode-cell and afterward collecting the fine metal therefrom.
Description
E. ANDRE. Separating Metals by Electrolysis.
No. 214,344. Patented April 15, 1879.
INVENTOR ATTORNEYS.
UNITED STATES PATENT OFFICE.
EMIL ANDRE, OF EHRENBREITSTEIN, GERMANY, ASSIGNOB TO PAUL HOLDER, OF NEW YORK, N. Y.
IMPROVEMENT IN SEPARATING METALS BY ELECTROLYSIS.
Specification forming part of Letters Patent No. 214,344, dated April 15, 1879; application filed April 18, 1878.
To all whom it may concern.-
Be it known that I, EMIL ANDRE, of Ehrenbreitstein, Germany, have invented certain Improvements in the Process and Apparatus for Refining and Separating Base Alloys by Electrolysis, of which the following is a specification.
It is the object of my invention to effect the refining and separating of base alloys and base metals by electrolysis. This object I effect by subjecting anodes composed of the base alloys or metals to be operated upon to the action of an electrolytic bath which is a solvent of the coarser metal or metals present in the anode, and which is contained in two cells or compartments, one for the anode and the other for the cathode, separated from each other by a porous diaphragm which is impermeable to the undissolved fine metal or metals, and also impermeable to the precipitate of a fine metal which may have been dissolved, and which. by reason of its porosity, serves to electrically connect the two cells. By means of my porous diaphragm I am enabled to effect the separation of the fine metal or metals from the base metal, either by precipitating such fine metal as may have been dissolved, and allowing the dissolved base metal to pass through the diaphragm into the cathode-cell, or by removing the solution from the anodecell as fast as the metals are dissolved, and thus retaining in the anode-cell such fine metal as is not soluble in the solution employed. In this way, in working upon the largest scale, it is easy to decompose by electrolysis anodes composed of several metals, and concurrently to separate the fine metal or metals from the base metal or metals.
My invention, therefore, consists in the combination, in the same electrolytic bath, of the operations of decomposing an anode of base alloy by dissolving only the coarser metals present in the anode, and of separating the undissolved fine metal from the dissolved base metal present.
It will, of course, be understood that the composition of my electrolytic bath or solution will be varied according to the various metals which may be contained in the alloy which isto be refined, and that the size and form of the cells containing the solution may be determined at the will of the constructer, and with reference to the magnitude of the operations contemplated; my invention being present when a porous diaphragm, separating the cells and affording a path for the electric current, is employed to detain in the anodecell an undissolved fine metal, while one or more coarser metals which have been dissolved are removed from the anodecell.
As the subject of electrolysis is well understood, it will be sufficient for me to describe my process as applied to the refining of an alloy composed of gold, silver, and copper.
I prefer to employ as the source of electricity a dynamo-electric machine, as I have found that such machines afiord the most economical means of generating the very strong currents of electricity which I use.
In applying my process to the purpose of refining a gold, silver, and copper alloy, I use for my electrolytic bath a saturated solution of sulphate of copper, containing, say, from three to five per cent. of free sulphuric acid.
My anodes are formed by casting the alloy into ingots of suitable form and size, and I employ a copper cathode or cathodes whose combined area equals that of the anodes. With such a solution the copper contained in the anode is first dissolved, and the solution then dissolves the silver. When the silver and copper are both dissolved the gold falls to the bottom of the cell in the form of slime, being prevented from passing into the oath ode-cell by my porous diaphragm. I may remove the solution of copper and silver from the anode-cell and collect the gold slime therefrom; or I may precipitate the silver which has been dissolved, and remove only the copper solution. For the precipitation of the silverI employ any of the known agents for this purpose, as, for example, the protoxide of iron. The removal from the anode-cell of the metals in solution may be effected by allowing them to pass through the porous diaphragm into the cathode-cell, or they may be remoyed by means of a pump or siphon. When the silver is precipitated in the anode-cell I collect it, together wi h the gold slime, after the removal of the copper solution, and separate the silver precipitate from the gold slime by redissolving the silver, using for this purpose any of the known solvents of silver. I then have remaining the pure gold which was originally contained in the alloyed anode. When the silver and copper solutions are removed together from the anode-cell I precipitate the silver by introducing the mixed solutions into a vat containing tine granulated copper. I then pour the remaining copper solution into my cathode-cell, where the copper from the solution is deposited in tnetallic t'orm upon the cathode, the deposit of the copper upon the cathode leaving the solution perfectly clear and fit to be again used.
A convenient apparatus suitable for the practice of my invention is illustrated in the ac companying drawings, in which Figure l is a vertical central section of an apparatus consisting of two cells, one above the other, separated hy two paral el diaphragms of porous material, establishing an intermediate chamber betwe n the cells. Fig. 2 is a. top view of the upper cell, and Fig. 3 a plan of the lower cell.
The apparatus represented in the drawings consists of the lower cell, A, which is a vat made of wood or other suitable material, and in which are suspended from a suitable frame the plates (1, that form the cathode. These plates are made of coppe plastic carbon, or other well-known material, according to the metal to be reduced.
At suitable height above the bottom of the lower or cathode cell, A, is another vat, ll, which is the anode-cell, in which the anodes b are suitably suspended.
The frames of the anode and cathode are, respectively, connected with the opposite poles of a dynamo-electric machine or other source of electricity.
The bottom of the anode-cell B is made of a diaphragm, ll, made of animal membrane orof porousclay, or some other material \v ich is impermeable to the undissolved metal, but sufliciently permeable to the solution to make it; a conductor of electricity, and thus ati'ord a free passage of the electric current from the solution in the anodecell to the solution in the cathodecell.
The dissolved metals in the solution maybe separated from the undissolved metal by being allowed to pass through the diaphragm from the anode-cell into the cathode-cell, or they may be removed by a siphon or pump. 1n the latter case, as one diaphragm might not be suflicient to prevent the passage of the dissolved metals into the cathodecell, a third in termedlate vessel, C, is employed, the bottom of which is also a porous diaphragm, C.
The intermediate space between the two d iaphragms is kept tilled with a constantly-running solution, that takes up and removes any of the solution which may have escaped from the anode-cell through the upper diaphram.
The surface of the anode is made equal to the surfaceot' the cathode, so that, more or less, the same area is brought into action at both electrodes.
The vats are provided with suitable rubber or other tubes, that supply the solutions or baths, and with siphous or outlet-pipes for re lnoving the same.
When gold, silver, and copper are to be severally separated from their alloys, such as gold or silver coins, base bullion, scraps, 850., these impure alloys are east into ingots, which are suspended in the anode-cell in the usual saturated solution of sulphate of copper, containing a small percentage of free sulphuric acid. Under the influence of the electrical current the copper and silver in the anode are successively dissolved, while the gold remains andissolved.
The anode and cathode plates may be arranged either in vertical position or in horizontal, inclined, or other position.
The dissolved metals may be drawn ofi' continuously from near the bottom of the anodecell. and fresh diluted acid added, as may be proportionately required.
The solution containing the dissolved copper and silver is conducted, preferably by gravity, to a conveniently-placed trough of suitable length, which is filled, in part, with granulated copper, on which the silver will be precipitated. The remaining solution, thus t'reed from silver, is conducted into a lower vat. in which the copper is precipitated in the usual manner. The remaining tree acid is then drawn off into a still lower vat, and diluted preparatory to being again used in the anodecell,as at first.
The top vat or anode-cell is supplied either with diluted acids or salts, according to the metals to be treated, and the liquid kept passing between thediaphragms is diluted acid or slightly acidulated water.
The arrangement of the baths or solutions and of the anode and cathode, and the materials employed, may, of course, be altered according to the different metals.
The apparatus may be worked with different solutions in thetop and bottom vats for dissolving one metal, ore, or combination in the acid solution of the top vat, While at the same time precipitating some other metal or salt from an ammoniacal or alkaline solution in the bottom vat.
I claim as my invention 1. The process of refining and separating base alloys or base metals herein described, which consists in subjecting such alloys as anodes to the electrolytic action of a solution which is a solvent of the coarser metals present, and in preventing the escape of the undissolved fine metals into the cathode-cell by interposing between the anode and cathode cells a porous diaphragm impermeable except to the metals in solution, and in removing the dissolved metals from the anode-cell and afterward collecting the fine metal therefrom.
2. In apparatus for "conducting the hereindescribed process of refining and separating base alloys, the combination of an anode and a cathode cell with two porous diaphragms, separating the cells and establishing between them an intermediate chamber, through which a current of liquid is maintained for the purpose of carrying off any portion of the solution from the anode-cell which may have penetrated such chamber, and thereby preventing such portion of the solution from entering the cathode-cell.
EMIL ANDRE. Witnesses H. HUFFMANN, F. SIEINDORF.
Publications (1)
Publication Number | Publication Date |
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US214344A true US214344A (en) | 1879-04-15 |
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US214344D Expired - Lifetime US214344A (en) | Improvement in separating metals by electrolysis |
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3793165A (en) * | 1971-12-27 | 1974-02-19 | Prototech Co | Method of electrodeposition using catalyzed hydrogen |
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0
- US US214344D patent/US214344A/en not_active Expired - Lifetime
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3793165A (en) * | 1971-12-27 | 1974-02-19 | Prototech Co | Method of electrodeposition using catalyzed hydrogen |
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