US949058A - Process for the treatment of silver-nickel-cobalt-arsenic ores. - Google Patents
Process for the treatment of silver-nickel-cobalt-arsenic ores. Download PDFInfo
- Publication number
- US949058A US949058A US52247509A US1909522475A US949058A US 949058 A US949058 A US 949058A US 52247509 A US52247509 A US 52247509A US 1909522475 A US1909522475 A US 1909522475A US 949058 A US949058 A US 949058A
- Authority
- US
- United States
- Prior art keywords
- silver
- arsenic
- copper
- nickel
- cobalt
- 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
- 238000000034 method Methods 0.000 title description 15
- PZKCBBCSJLOHFS-UHFFFAOYSA-N [As].[Co].[Ni].[Ag] Chemical compound [As].[Co].[Ni].[Ag] PZKCBBCSJLOHFS-UHFFFAOYSA-N 0.000 title 1
- 229910052785 arsenic Inorganic materials 0.000 description 23
- 229910052802 copper Inorganic materials 0.000 description 23
- 239000010949 copper Substances 0.000 description 23
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 21
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 21
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 20
- 229910052709 silver Inorganic materials 0.000 description 20
- 239000004332 silver Substances 0.000 description 20
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 12
- 239000003792 electrolyte Substances 0.000 description 10
- 239000002184 metal Substances 0.000 description 8
- 229910052751 metal Inorganic materials 0.000 description 8
- 229910017052 cobalt Inorganic materials 0.000 description 7
- 239000010941 cobalt Substances 0.000 description 7
- 235000013495 cobalt Nutrition 0.000 description 7
- 150000002739 metals Chemical class 0.000 description 7
- 238000003723 Smelting Methods 0.000 description 6
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 6
- 229910052759 nickel Inorganic materials 0.000 description 6
- 238000005868 electrolysis reaction Methods 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 239000000956 alloy Substances 0.000 description 4
- 229910045601 alloy Inorganic materials 0.000 description 4
- QXZUUHYBWMWJHK-UHFFFAOYSA-N [Co].[Ni] Chemical compound [Co].[Ni] QXZUUHYBWMWJHK-UHFFFAOYSA-N 0.000 description 3
- 230000004907 flux Effects 0.000 description 3
- 239000013065 commercial product Substances 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- LEHOTFFKMJEONL-UHFFFAOYSA-N Uric Acid Chemical compound N1C(=O)NC(=O)C2=C1NC(=O)N2 LEHOTFFKMJEONL-UHFFFAOYSA-N 0.000 description 1
- TVWHNULVHGKJHS-UHFFFAOYSA-N Uric acid Natural products N1C(=O)NC(=O)C2NC(=O)NC21 TVWHNULVHGKJHS-UHFFFAOYSA-N 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000009388 chemical precipitation 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
- 239000000203 mixture Substances 0.000 description 1
- 235000020004 porter Nutrition 0.000 description 1
- 229940116269 uric acid Drugs 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
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
- The. invention relates to the treatment of- Canadian or other ores which contain, besides silver, considerable quantities of nickel, cobalts, and especially arsenic.
- ores run as follows: silver 800 to 10,000 ounces to the ton; nickel and cobalt 10 to arsenic 5 to lead none. 1
- the invention consists in the process and subrocesses hereinafter more particularly set orth,- whereby throu h electrolysis of an anode of the alloy produced by smelting said ore in thepresen'ce of copper, the metals are separated, so that alLof the silver may be recovered as a high grade product from the slimes, all of the nickel and cobaltis dissolved in the electrolyte together with copper is deposited in substantially pure to a certain number of ounces state on the cathode.
- the copper percentage should be increased .to 25 per cent. If the silver present amounts per ton, the amount of copper should not be less. lBesides the copper the necessary quantity of usual fluxes is to be added. By this smelting operation is produced an'ialloy containingp besides copper, all'the silver, nickel and cobalt and nearly all the arsenic in the ore treated. This is tapped from the furnace into molds of suitable shape to produce anodes for the electrolytic operation which next follows.
- the cathodes are to be sheets of pure copper.
- the electrolyte is a solution of cop er sulfate in water, and during the whole e ectrolytic operation the solution should contain at least ten Specification of Letters Patent.
- the density of the' electric current is to be regulated according to the composition of the anode and of the electrolyte. If the anode alloy varies in percentage of. silver and arsenic, the density of the current should correspondingly vary. The density will be increased proportionately to the quantity of copper in the electrolyte;
- the temperature of the bath is preferably to be about degrees centigrade; but is regulated by the percentage of arsenic in the anode. The higher this percentage, the higher should, be the temperature so as tobring as much of the ar-' senic is possible into the solution. 7
- trolyte containing the Whole of the nickelcobalt and the larger part of the arsenic can be brought up to the follow ng concentrations: silver none; copper 10 grams per liter; nickel-cobalt 55 grams per liter;
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Electrolytic Production Of Metals (AREA)
Description
. the larger CAMILLO C. CITO, IRVING-TON, NEW JERSEY.
PROCESS FOR THE TREATMENT OF SILVER-NICKEL-COIiALT-ARSENIC ORES.
9419,05d. no Drawing.
To all whom it may concern: I
Be it known that I, CAMILLo C. Crro, a
subject of the Grand Duke of Luxemburg,
residing at Irvington, in the county of BS- 1 sex'and State of New Jersey, have invented a certain new and useful Improvement in Processes for the Treatment of Silver- Nickel-Cobalt-Arsenlc Ores, of which .the
following is a specification.
The. invention relates to the treatment of- Canadian or other ores which contain, besides silver, considerable quantities of nickel, cobalts, and especially arsenic. Generally, such ores run as follows: silver 800 to 10,000 ounces to the ton; nickel and cobalt 10 to arsenic 5 to lead none. 1
-The invention consists in the process and subrocesses hereinafter more particularly set orth,- whereby throu h electrolysis of an anode of the alloy produced by smelting said ore in thepresen'ce of copper, the metals are separated, so that alLof the silver may be recovered as a high grade product from the slimes, all of the nickel and cobaltis dissolved in the electrolyte together with copper is deposited in substantially pure to a certain number of ounces state on the cathode.
In carrying out my process I proceed as follows: The ore smelted in a reverberatory furnace without any preliminary treatment, such asroasting, etc. I add to said ore a percentage of copper, preferably equal to two thirds that of thenickel and cobalt and at least the same as that of the arsenic, and not less .in amount than the silver. Thus I may put in 20 per cent. of'copper,
,but if there is 25 per cent. of arsenic present,
the copper percentage should be increased .to 25 per cent. If the silver present amounts per ton, the amount of copper should not be less. lBesides the copper the necessary quantity of usual fluxes is to be added. By this smelting operation is produced an'ialloy containingp besides copper, all'the silver, nickel and cobalt and nearly all the arsenic in the ore treated. This is tapped from the furnace into molds of suitable shape to produce anodes for the electrolytic operation which next follows.
In the electrolytic bath, the cathodes are to be sheets of pure copper. The electrolyte is a solution of cop er sulfate in water, and during the whole e ectrolytic operation the solution should contain at least ten Specification of Letters Patent.
Application filed October13, 1909. Serial No. 522,475.
part of the arsenic, and all of the Patented Feb. is, into.
uric acid per liter. The density of the' electric current is to be regulated according to the composition of the anode and of the electrolyte. If the anode alloy varies in percentage of. silver and arsenic, the density of the current should correspondingly vary. The density will be increased proportionately to the quantity of copper in the electrolyte; The temperature of the bath is preferably to be about degrees centigrade; but is regulated by the percentage of arsenic in the anode. The higher this percentage, the higher should, be the temperature so as tobring as much of the ar-' senic is possible into the solution. 7
The result of the'electrolysis is practi-- cally lows:
1. Silver. All in the anode is precipitated in the'slimes.
2. Nickel-cobalt. All in the, anode remains quantitatively dissolved in the electrolyte.
quantitatively 3. Arsenic. The largest part of that in the anode remains dissolved in the electrolyte, the balance going into the slimes with the silver.
4. Copper. All in the anode is deposited in the form of pure electrolytic copper on. the cathode. A determination of this has yielded 99.98% Cu. Or, in other words,'the copper originally added as'a dlux is recovered as a commercial product.
And it is further to be noted that no gases which, on account of the arsenic, would be very dangerous, are developed during the electrolysis.
To state the result of the process in another wayI have distributed the metals of the anode respectively in diflerent places in the bath. On the cathode, is all the copper. In the slimes is all the silver and a small portion of the arsenic. In the electrolyte is all the nickel and cobalt and the greater part of the arsenic. As a consequence. of this distribution, the further treatment of the products is very simple.
Treatment 0 the sZimes.-These are rich or poor, accor( ing to the percentage of silver in the anode, but under all circumstances. they contain all the silver, since no traces of that metal ap ear either in the cathode or electrolyte. T e small amount of arsenic which enters the slimes, together with the silver, can easily be removed by a light roasting or a dissolving process. Thus, an ore orlginally contammgGOO 02s. of silver per ton, 19% arsenic, and'17.5% nlckel-cobalt, yielded slimes of 12,000 ozs. silver per ton; While the slimes of another orv that ran 3,500 ozs. of silver per ton contained 24,500
' trolyte containing the Whole of the nickelcobalt and the larger part of the arsenic can be brought up to the follow ng concentrations: silver none; copper 10 grams per liter; nickel-cobalt 55 grams per liter;
arsenic 30 grams per liter. From this solution, the larger part of the copper can be precipitated by the electric current, using a carbon anode. The remainder of the copper is :ulvantageously precipitated by H S' in the'cold, whereby very little sulfid of arsenic is formed. This copper product can be used over as a flux. All the arsenic can then be precipitated by H S in the heat, as sulfid of arsenic, which can be placed on the market as such. Nickel and cobalt can now be recovered, together or separate, by any of the methods usually e1nployedeither by electrolysis or by chemical precipitation. 4
Particular attention is now called to the following facts resulting from my aforesaid process. 1. I obtain a direct output of the principal metals. limiting,'at the same time, the forming of by-products. 2. From a complex anode, I deposit pure copper on the cathode. 3. The metals are extracted and deposited from the anode and not from the electrolyte. 4. The operation is exceedingly simple, and hence involves very low running expenses; 5. The most important metals are brought out with great rapidity: especially the silver which is recovered as a high grade product which, without difficulty, can be refined by any known process. 6. Despite the possible large amount of arsenic present,
danger from arsenious gases is practically elimlnated. 7. The copper added as flux is regained in the electrolytic operation as a commercial product. 8. By reason of the distribution of metals and of the quantitative deposit of all the silver in the slimes, I do not produce a plurality of different products, each containing more or less silver and each requiring separate treatment for its removal In another application for Letters Patent Serial No. 522,476 filed by me simultaneously herewith, I have described and claimed the process of smelting silver-nickel-cobaltarsenic ore, free from lead, in the presence of copper, which smelting process forms a step in mypresent process, and therefore, I do not claim said smelting process herein.
I claim:
1. The process of treating a silver-nickelcobalt-arsenic ore free from lead, which consists in first, smelting the ore in the presence cobalt and nearly all the arsenic, and second,
separating the metals by electrolysis from an anode of said alloy in an electrolyte containing copper sulfate.
In testimony whereof I have afiixed my signature in presence of two witnesses.
CAMILLO o. crro.
\Vitnesses Gnu'rnuon T. PORTER, MAY T. MGGARRY.
of copper to produce. an alloy containing
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US52247509A US949058A (en) | 1909-10-13 | 1909-10-13 | Process for the treatment of silver-nickel-cobalt-arsenic ores. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US52247509A US949058A (en) | 1909-10-13 | 1909-10-13 | Process for the treatment of silver-nickel-cobalt-arsenic ores. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US949058A true US949058A (en) | 1910-02-15 |
Family
ID=3017472
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US52247509A Expired - Lifetime US949058A (en) | 1909-10-13 | 1909-10-13 | Process for the treatment of silver-nickel-cobalt-arsenic ores. |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US949058A (en) |
-
1909
- 1909-10-13 US US52247509A patent/US949058A/en not_active Expired - Lifetime
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