US704393A - Manufacture of iron, manganese, and alloys of these metals by aid of electricity. - Google Patents
Manufacture of iron, manganese, and alloys of these metals by aid of electricity. Download PDFInfo
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- US704393A US704393A US4912001A US1901049120A US704393A US 704393 A US704393 A US 704393A US 4912001 A US4912001 A US 4912001A US 1901049120 A US1901049120 A US 1901049120A US 704393 A US704393 A US 704393A
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- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25C—PROCESSES FOR THE ELECTROLYTIC PRODUCTION, RECOVERY OR REFINING OF METALS; APPARATUS THEREFOR
- C25C3/00—Electrolytic production, recovery or refining of metals by electrolysis of melts
- C25C3/34—Electrolytic production, recovery or refining of metals by electrolysis of melts of metals not provided for in groups C25C3/02 - C25C3/32
Definitions
- the lower oxids of manganese are soluble in fused fluorid of calcium.
- This solution can be used as the electrolyte, and it will yield metallic manganese at the cathode under the action of acontinuous electric current suitable to produce simultaneously the electrolytic decomposition and thermic action necessary for melting the mixture and keeping it in a sufliciently fluid condition.
- the composition of the electrolyte be such that its point of fusion be Vnot sensibly greater than that of the manganese (1,500o to 1,400o centigrade) and if this composition be kept about constant by regulated additions of oxid of manganese, the formation of the metallic bath will be continuous and the temperature moderate enough to enable the metal to be drawn off, while avoiding volatilization and the losses it entails.
- the reduction of the silicates contained in the ore the same retains onlyT a smallquantity of silicon, and it Will be evident that the silicon which results from the reduction of the silicates by the action of the electric current combines with the iuorin to form a gaseous iuorid. It is well known that the affinity or tendency of silicon combining with iuorin and, as before stated, the metal only retains l a small quantity of the silicon.
- the electrolytic treatment can be employed alone or combined with the reduction by carbon.
- the electrolytic method when the electrolytic method is alone resorted to the normal voltage varies from seven to eight volts for a current intensity of five to six amperes perl square centimeter.
- the silicon reduced under the action of the current combines with the free fluorin to form a gaseous iiuorid, which is set free, so that the metal only retains but small quantities of silicon.
- the silicon reduced When the electrolytic treatment is combined with the reduction by the carbon, the silicon reduced, owing to the presence of the carbon in the bath, combines, as aforesaid, with the free fiuorin to form a gaseous iiuorid, which is set free, so that the metal only retains a small quantity of silicon.
- the normal voltage may be greatly increased, even to as high as eighteen or twenty volts.
- rlhis furnace consists, essentially, of a crucible or hearth a., of a fireproof material of any suitable composition, mounted on a carriage h and provided With raised sides c.
- the cathode is formed of horizontal carbons d, arranged on the base of the hearth or crucible, the casing of which they traverse, and they are connected to the main circuit f by means of flexible connections pressed against the carbons by plates e.
- These carbons d are embeddedin a layerg of crushed ferromanganese, the upper level ⁇ of which rises about to three-fourths of the height of the casing a.
- the purpose of this layer of crushed ferromanganese is to form a conductive mass with the bath of molten metal, as will be more clearly explained below.
- upper electrode or anode is formed of four (or more) electric carbons h, which are of dimensions proportionate to the power of the furnace and which can be moved vertically by means of levers or the like.
- the carbons which form the upper electrode h are inclosed in a casing or envelop j of crushed slag com@ pressed with tar and resin.
- the manganese contained in this slag is monoxid, so it cannot promote the oxidation of the carbons.
- This form of this electrode is that of a rectangular prism sliding in a frame k, provided on its four sides with charging-openings n.
- the raised sides c carry brackets o at their upper ends placed under the brickwork p, so as to securely close the interior of the furnace.
- a channel q is provided in the brickwork p, the said channel communicating by means of openings 1* with the interior of the furnace and also with adjustt-chamber, into which the gases arising from the reduction process pass, together with the metallic dust and vapors.
- Two small blocks of carbon are arranged at s s, which blocks extend just above the top of the layer of crushed ferromanganese g and serve to prime the furnace, for Without these the current could not pass at a low temperature through the said layer of crushed ferroman ganese,which then offers too considerable resistance.
- the operation is the following: After the upper electrodes h have been placed in contact with the carbon blocks s a mixture of flour-spar and carbon is gradually introduced through the openings fn, the constituents being in proportions suited to the voltage at which the furnace is working.
- the strength or intensity of the electric current in the said y carbon blocks s being very high by reason produced which finally reaches a normal and invariable degree corresponding to the minimum of volatilization of the metal, if the proper strength or intensity of electric current be provided.
- a current for example, of, say, forty to fifty watts per square centimeter of the sectional area of the upper electrode enables this result to be obtained.
- the metal As the work of the furnace proceeds the metal accumulates on the hearth g, Where it remains in a fluid condition by reason of the superficial resistance of the layer and its low thermic conductibility. When the bath of metal has reached the desired height, it is drawn off in the usual manner.
- the present method also allows the obtainment of rich ferromanganese or other alloys of metals. For this purpose there is only to be introduced into the fuel mixture a suitable proportion of an oxid of the metal which is to enter in the composition of the alloy.
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- Organic Chemistry (AREA)
- Electrolytic Production Of Metals (AREA)
Description
No. 704,393. E Patented July s, |902.
y A. slmon. I l MANUFACTUBE 0F IRON, MANGANESE, AND ALLOYS-OF THESE METALS BY AID 0F ELECTRICITY.
' (Application filed Feb. 27, 1901.) (No Model.)
STATES ALBERT SIMON, OF i5 PATENT Clarion."
ORDEAUX, FRANCE.
MANUFACTURE OF IRON, MANGANESE, AND ALLOYS 0F THESE METALS BY AID 0F ELECTRICITY.
SPECIFICATION forming part of Letters Patent No. 704,393, dated July 8, 1902. Application tiled February 27, 1901. Serial No. 49,120. (No specimens.)
To @ZZ whom, it rita/y concern:
Be it known that I, ALBERT SIMON, engineer, a citizen of the French Republic, resid` ess intended to render practicable the use of electric furnaces for obtaining the said products on a commercial scale. Attempts hitherto :made to obtain such products in the electric furnace by reduction of the ores in the presence of carbon have not proved satisfactory, owing principally to the considerable loss of metal owing to the readiness of the manganese to volatilize.
This invention is based on the practical carrying into effect of the following observations: The lower oxids of manganese are soluble in fused fluorid of calcium. This solution can be used as the electrolyte, and it will yield metallic manganese at the cathode under the action of acontinuous electric current suitable to produce simultaneously the electrolytic decomposition and thermic action necessary for melting the mixture and keeping it in a sufliciently fluid condition. If the composition of the electrolyte be such that its point of fusion be Vnot sensibly greater than that of the manganese (1,500o to 1,400o centigrade) and if this composition be kept about constant by regulated additions of oxid of manganese, the formation of the metallic bath will be continuous and the temperature moderate enough to enable the metal to be drawn off, while avoiding volatilization and the losses it entails. By the employment of the method set forth hereinafter the reduction of the silicates contained in the ore the same retains onlyT a smallquantity of silicon, and it Will be evident that the silicon which results from the reduction of the silicates by the action of the electric current combines with the iuorin to form a gaseous iuorid. It is well known that the affinity or tendency of silicon combining with iuorin and, as before stated, the metal only retains l a small quantity of the silicon.
` According to this invention the electrolytic treatment can be employed alone or combined with the reduction by carbon. In the first case, say, when the electrolytic method is alone resorted to the normal voltage varies from seven to eight volts for a current intensity of five to six amperes perl square centimeter. The silicon reduced under the action of the current combines with the free fluorin to form a gaseous iiuorid, which is set free, so that the metal only retains but small quantities of silicon. When the electrolytic treatment is combined with the reduction by the carbon, the silicon reduced, owing to the presence of the carbon in the bath, combines, as aforesaid, with the free fiuorin to form a gaseous iiuorid, which is set free, so that the metal only retains a small quantity of silicon. In this case of simultaneous employment of electrolysis and reduction by carbon the normal voltage may be greatly increased, even to as high as eighteen or twenty volts.
For the practical carrying out of the process an electric furnace may be used of the kind described in my application for United States Patent, Serial No. 49,119, dated February 27, 1901,0f which the accompanying drawing is a sectional view. rlhis furnace consists, essentially, of a crucible or hearth a., of a fireproof material of any suitable composition, mounted on a carriage h and provided With raised sides c. The cathode is formed of horizontal carbons d, arranged on the base of the hearth or crucible, the casing of which they traverse, and they are connected to the main circuit f by means of flexible connections pressed against the carbons by plates e. These carbons d are embeddedin a layerg of crushed ferromanganese, the upper level `of which rises about to three-fourths of the height of the casing a. The purpose of this layer of crushed ferromanganese is to form a conductive mass with the bath of molten metal, as will be more clearly explained below. The
upper electrode or anode is formed of four (or more) electric carbons h, which are of dimensions proportionate to the power of the furnace and which can be moved vertically by means of levers or the like. The carbons which form the upper electrode h are inclosed in a casing or envelop j of crushed slag com@ pressed with tar and resin. The manganese contained in this slag is monoxid, so it cannot promote the oxidation of the carbons. This form of this electrode is that of a rectangular prism sliding in a frame k, provided on its four sides with charging-openings n. The raised sides c carry brackets o at their upper ends placed under the brickwork p, so as to securely close the interior of the furnace. A channel q is provided in the brickwork p, the said channel communicating by means of openings 1* with the interior of the furnace and also with adust-chamber, into which the gases arising from the reduction process pass, together with the metallic dust and vapors., Two small blocks of carbon are arranged at s s, which blocks extend just above the top of the layer of crushed ferromanganese g and serve to prime the furnace, for Without these the current could not pass at a low temperature through the said layer of crushed ferroman ganese,which then offers too considerable resistance.
The operation is the following: After the upper electrodes h have been placed in contact with the carbon blocks s a mixture of flour-spar and carbon is gradually introduced through the openings fn, the constituents being in proportions suited to the voltage at which the furnace is working. The strength or intensity of the electric current in the said y carbon blocks s being very high by reason produced which finally reaches a normal and invariable degree corresponding to the minimum of volatilization of the metal, if the proper strength or intensity of electric current be provided. A current, for example, of, say, forty to fifty watts per square centimeter of the sectional area of the upper electrode enables this result to be obtained. As the work of the furnace proceeds the metal accumulates on the hearth g, Where it remains in a fluid condition by reason of the superficial resistance of the layer and its low thermic conductibility. When the bath of metal has reached the desired height, it is drawn off in the usual manner. The present method also allows the obtainment of rich ferromanganese or other alloys of metals. For this purpose there is only to be introduced into the fuel mixture a suitable proportion of an oxid of the metal which is to enter in the composition of the alloy.
Having now particularly described and ascertained the nature of my invention and in what manner the same may be performed, I declare that what I claim is- A process of manufacturing iron, manganese and the alloys of such metals, consisting in adding to the material to be treated carbon, and an electrolyte consisting of liuorid of calcium, in sufficient quantity to dissolve the material and then subjecting the mass to the action of a continuous electric current to cause the electrolytic decomposition and the keeping of the material in a liuid condition, substantially as described and for the purd pose set forth.
In testimony whereof I have hereunto set my hand in presence of two subscribing Witnesses. v
ALBERT SIMON.
Witnesses:
JAMES L. OHAssEREAU, GABRIEL FAURE.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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US4912001A US704393A (en) | 1901-02-27 | 1901-02-27 | Manufacture of iron, manganese, and alloys of these metals by aid of electricity. |
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US4912001A US704393A (en) | 1901-02-27 | 1901-02-27 | Manufacture of iron, manganese, and alloys of these metals by aid of electricity. |
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US704393A true US704393A (en) | 1902-07-08 |
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US4912001A Expired - Lifetime US704393A (en) | 1901-02-27 | 1901-02-27 | Manufacture of iron, manganese, and alloys of these metals by aid of electricity. |
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Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2913381A (en) * | 1955-08-18 | 1959-11-17 | Nat Distillers Chem Corp | Start up method for fused salt electrolytic cells |
DE1179723B (en) * | 1961-11-23 | 1964-10-15 | Manganese Chemicals Corp | Process and device for the electrolysis of iron-containing manganese |
US3450524A (en) * | 1965-11-03 | 1969-06-17 | Ugine Kuhlmann | Process for the preparation of pure manganese |
US4157285A (en) * | 1975-05-27 | 1979-06-05 | Universite Libre De Bruxelles | Method for preparing manganese chloride and manganese by igneous electrolysis of the manganese chloride obtained |
US4224119A (en) * | 1979-08-10 | 1980-09-23 | Chemetals Corporation | In-cell manganese ore reduction |
US4349427A (en) * | 1980-06-23 | 1982-09-14 | Kaiser Aluminum & Chemical Corporation | Aluminum reduction cell electrode |
US4410403A (en) * | 1980-06-17 | 1983-10-18 | Aluminum Company Of America | Electrolysis method |
-
1901
- 1901-02-27 US US4912001A patent/US704393A/en not_active Expired - Lifetime
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2913381A (en) * | 1955-08-18 | 1959-11-17 | Nat Distillers Chem Corp | Start up method for fused salt electrolytic cells |
DE1179723B (en) * | 1961-11-23 | 1964-10-15 | Manganese Chemicals Corp | Process and device for the electrolysis of iron-containing manganese |
US3450524A (en) * | 1965-11-03 | 1969-06-17 | Ugine Kuhlmann | Process for the preparation of pure manganese |
US4157285A (en) * | 1975-05-27 | 1979-06-05 | Universite Libre De Bruxelles | Method for preparing manganese chloride and manganese by igneous electrolysis of the manganese chloride obtained |
US4224119A (en) * | 1979-08-10 | 1980-09-23 | Chemetals Corporation | In-cell manganese ore reduction |
WO1981000421A1 (en) * | 1979-08-10 | 1981-02-19 | Chemetals Corp | In-cell manganese ore reduction |
US4410403A (en) * | 1980-06-17 | 1983-10-18 | Aluminum Company Of America | Electrolysis method |
US4349427A (en) * | 1980-06-23 | 1982-09-14 | Kaiser Aluminum & Chemical Corporation | Aluminum reduction cell electrode |
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