US1821176A - Method of preparing rare refractory metals - Google Patents

Method of preparing rare refractory metals Download PDF

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US1821176A
US1821176A US309682A US30968228A US1821176A US 1821176 A US1821176 A US 1821176A US 309682 A US309682 A US 309682A US 30968228 A US30968228 A US 30968228A US 1821176 A US1821176 A US 1821176A
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chromium
bath
rare refractory
metal
compounds
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US309682A
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Frank H Driggs
John W Marden
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Westinghouse Lamp Co
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Westinghouse Lamp Co
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    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25CPROCESSES FOR THE ELECTROLYTIC PRODUCTION, RECOVERY OR REFINING OF METALS; APPARATUS THEREFOR
    • C25C3/00Electrolytic production, recovery or refining of metals by electrolysis of melts
    • C25C3/34Electrolytic production, recovery or refining of metals by electrolysis of melts of metals not provided for in groups C25C3/02 - C25C3/32
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25CPROCESSES FOR THE ELECTROLYTIC PRODUCTION, RECOVERY OR REFINING OF METALS; APPARATUS THEREFOR
    • C25C3/00Electrolytic production, recovery or refining of metals by electrolysis of melts
    • C25C3/32Electrolytic production, recovery or refining of metals by electrolysis of melts of chromium

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  • 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

Patented Sept. 1, 1931 OFFICE FRANK H. DRIGGS, OF BLOOMFIELD, AND JOHN W. MARDEN, OF EAST ORANGE, NEW JERSEY, ASSIGNORS TO WESTINGHOUSE LAMP COMPANY, A CORPORATION OF PENNSYLVANIA METHOD OF PREPARING RARE REFRACTORY METALS No Drawing.
This invention relates to the art of metallurgy and more particularly to the art of electro-metallurgy and comprises essentially a method of producing the rare refractory metals by the electrolysis of fused baths. More particularly the invention is directed to the provision of a suitable fused bath from which certain of the rare refractory metals may be produced by electro-chemical means which metals have been heretofore unobtainable or difiicultly obtainable by such means.
In copending applications Serial No. 275,264, filed May 4, 1928 and Serial No. 277,096, filed May 11, 1928, both by Frank H. Briggs and assigned to the same assignee as the present application, are described two methods for the production of rare refractory metals by electrolytic dissociation of their fused salts. One of these methods is particularly applicable to the production of tantalum and similar metals and the other process is specifically directed tothe production of uranium although not limited to this metal.
in the production of the rare refractory metals of the group known as chromium,
tungsten, molybdenum and also uranium, by electro-metallurgical methods, difficulty is experienced in preventing the formation of highly refractory and highly inert and insoluble oxide compounds. The usual fused bath heretofore employed inthe electrolysis of these metals has been non-reactive with respect to these oxide compounds and care must be taken to utilize compounds of these metals therein which are highly stable at elevated temperatures and non-decomposable to such oxygen carrying compounds. Such suitable compounds have been described in the above identified copending application Serial 'No. 277 ,096.
Whereas the process as described in the said copending application is specifically successful in preparing the rare refractory metals by electrolysis the preparation of the anhydrous, non-oxygen carrying compounds 'KUF or K CrF to utilize therein introduces an added step in the process which it is one of the objects of this invention to eliminate.
Application filed October 1, 1928. Serial No. 309,682.
Another object of the present invention is to provide a fused bath which is reactive with the oxygen containing compounds of the rare refractory metals of this particular group.
Another object of this invention is to provide an electro-metallurgical method for the production of these metals from a fused bath containing oxygen-carrying compounds of said metals.
Another object of thisinvention is to provide a relatively cheap economical and highly efiicient means of preparing the substantially pure rare refractory metal powders of the chromium, uranium, tungsten, and molybdenum group, so that they may subsequently be compacted, sintered into coherent ingots and mechanically deformed to desired shapes and sizes. I
Other objects and advantages may be apparent as the invention is more fully disclosed.
In accordance with our invention we utilize as the fused bath, an alkaline earth metal halide, such as calcium chloride, to which we may add in Various proportions, depending upon the particular metal of the group being prepared, the particular compound employed, the temperature of the bath, and other factors; a compound of the refractory metal, such as the oxide, a double alkali metal halide, such as the double potassium chromium chloride or fluoride, or the halogen compound (anhydrous) or any desirable mixture of the above mentioned compounds.
This fused bath is then decomposed by the passage of an electric current threthrough and the rare refractory metal component deposited therefrom. Subsequently the cooled fused bath is lixiviated with water and the calcium chloride dissolved away and the metal powder remaining digested with suitable acid solvents to remove deleterious impurities. The metal powder is then dried with alcohol and ether and subsequently compacted and sintered into a coherent metal body If desired, the process may be made a continuous one by frequent additions to the fused bath of additional amounts of the chloride,
rare refractory metal compound as the content thereof is exhausted.
According to the disclosure in copending application Serial No. 277,096, it is extremely diflicult to prevent the formation of oxygencarrying compounds of chromium and. uranium during the electrolytic dissociatlon of their fused salts and that it is essential to employ a highly stable nonoxygen carrying double halogen compound such as the double potassium uranium fluoride, having the formula KUF, prepared by the method as disclosed in a copending application Serial No. 168,826, entitled Preparation of an oxidefree halide of a rare refractory metal, and assi ed to the same assignee as. the present app ication.
We have determined that alkaline earth metal chlorides, particularly calcium chloride, has a sufiicient solubility for oxide compounds of the above identified group of metals and particularly for uranium oxide and chromium oxide compounds so that it may be successfully employed as the fluxing agent of an electro-metallurgical bath instead of or as substantially replacing the mixture of alkaline and alkaline earth metal fluorides heretofore employed.
We have also determined that the use of this particular fluxing agent in the specific production of this group of metals by electrolysis, provides a means of obtaining the metals in this group in a cheaper, simpler and more eflicient manner than heretofore possible.
The electrolysis may be carried out in a carbon, graphite or nickel crucible or the crucible may be comprised of any material or alloy which is substantially non-reactive with the alkaline earth metal chloride, but it should be preferably sufliciently conductive to act as the cathode of the cell.
As a specific embodiment of the nature of our invention we will describe the invention as applied to the production of the rare refractory metal chromium although we have been equally successful in the application of the basic principle of the invention in the production of the other metals of the same family group.
We first form a fused bath of calcium chloride in a carbon, graphite or preferably nickel crucible, to which is added in amounts sufficient to saturate the bath, a suitable chromium compound such as chromium chromium potassium chloride (K CrCl chromium potassium fluoride (K CrF or chromium oxide (0130,) or any desirable combination of these compounds. We may add, for instance, to the fused bath, chromium potassium chloride in amounts up to 20 percent or so and thereafter to the fused bath add suflicient chromium oxide to saturate the bath. Or we may add to the bath the chromium oxide alone, in which case we have found that the calcium chloride will dissolve approximately 2 percent of its weight of chromium oxide. The specific components of the bath we prefer to employ contains the following ingredients:
' Gram: Calcium chloride 150 Chromium oxide 7 Or chromium chloride 14 Or chromium potassium chloride 20 Or chromium potassium fluoride 18 The electrolysis may be allowed to con-.
tinue until all of the chromium content has been dissociated into metal and if desired, may be made a continuous one through the addition from time to time of fresh chromium oxide, chromium chloride or other fusible and ionizable chromium containing compound. By calculating the current equivalent factor for the particular chromium compound utilized and then adjusting the ampere hours to be greater than this equivalent, the bath at the conclusion of the run may be made substantially free of chromium oxide.
At the conclusion of the run the fused bath is allowed to cool to room temperature and then washed with distilled water to remove the soluble calcium chloride. The deposited metal powder, which will be found accumulated along the side of the cathode crucible, is
.then successively Washed with dilute nitric acid, water, alcohol and ether and then thoroughly dried in vacuo. The resultant metal powder should then be sieved through a fine mesh screen, compacted into suitable shapes and sizes and sintered by well known metallurgical means into a coherent ingot. Thereafter the ingot may be reduced to desired shapes and sizes by Well known mechanical deformation methods.
Whereas we have specifically described the invention as relates to the production of metallic chromium powder it is obvious that many departures may be made from the specific embodiment without essentially departing from the nature of the invention and all such departures and variations are anticipated as may fall within the scope of the following claims.
What is claimed is:
1. The method of preparing the rare refractory metals of the group known as tungsten, molybdenum, chromium and uranium, which comprises electrolytically decomposing a fused bath containing dissociable compounds of the rare refractory metal, said bath being comprised in ma or part of a chemical compound having a solubilit towards the oxygen carrying compoun s of said rare refractory metals to form compounds therewith substantially dissociable by the electric current.
2. The method of preparing the rare refractory metals of the group known as tungsten, molybdenum, chromium and uranium,
which comprises electrolytically decomposing a fused bath containing dissociable compounds of said rare refractory metals, said bath being comprised in major part of an alkaline earth metal halide reactive with re- 2 spect to the oxygen carrying compounds of said rare refractory metals to form compounds substantially dissociable by the electric current.
3. The method of preparing chromium metal powder which comprises electrolytically decomposing a fused bath containing dlssociable compounds of chromium, said bath being comprised in major part of an alkaline earth metal halide reactive with respect with oxygen carrying compounds of chromium to form compounds therewith which are substantially dissociable by the electric current. 4. The method of preparing chromium metal powder which comprises electrolytical- 1y decomposing a fused bath comprised 1n major part of calcium chloride and containing a proportion of a halogen compound of chromium together with approximately 2% chromium oxide.
5. The method of preparing chromium which comprises electrolytically decomposing a fused bath comprised in major part of calcium chloride and containing a proportion of a dissociable chromium compound and adding thereto at frequent intervals increments of additional dissociable chromium compounds such as chromium oxide.
6. The method of preparing rare refractory metal powders of the tungsten, molybdenum, chromium and uranium class which comprises electrolytically depositing said metal powders from a fused bath comprised in major part of cal ium chloride to which have been added a proportion of a dissociable rare refractory metal compound fusible and soluble in said calcium chloride. prolonging the time of said electrolytic deposition by means of adding thereto at frequent intervals additional amounts of said rare refractory metal compound, continuing said electrolysis until substantially all of the oxygen carrying compounds of said refractory metal has been decomposed and removed from said fused bath, thereafter cooling the fused bath C5 to room temperature, efiecting a separation of said electrolyticall deposited metal from the aqueous and aci soluble residual component of said bath, and collecting the remaining refractory metal powder.
7. The method of preparing chromium.
thereafter cooling the fusion and recovering the deposited metal powder from the cooled fused mass by dissolving away the water and acid soluble impurities in any desired manner.
8. The method of preparing the rare refractory metal powders of the tungsten, molybdenum, chromium, uranium group which comprises electrolytically depositing the rare refractory metal powder from a fused bath comprised of an alkali earth metal chloride containing a proportion of a double halide compound of said rare refractory metal.
9. The method of preparing the rare refractory metal powders of the tungsten, molybdenum, chromium, uranium oup, which comprises electrolytically depositing the rare refractory metal powder from a fused bath comprised of calcium chloride containing a proportion of a double halide compound of said rare refractory metal.
10. The method of preparing the rare re fractory metal powders of the tungsten, molybdenum, chromium, uranium group, which comprises electrolytically depositing the rare refractory metal powder from a fused bath comprised of calcium chloride containing a proportion of a double halide compound of said rare refractory metal and a proportion of an oxygen containing compound of the rare refractory metal.
11. The method of preparing,chromium metal powder which comprises electrolytically depositing the metal in powder form from a fused bath comprised of calcium chloride containing a proportion of an ionizable chromi'um compound.
12. The method of preparing chromium metal powder which comprises electrolytically depositing the metal in powder form from a fused bath comprised of calcium chloride containing a proportion of a double halide compound of chromium.
13. The method of preparing chromium metal powder which comprises electrolytically depositing the metal in powder form from a fused bath comprised of calcium chloride containing a proportion of a double hatember, 1928.
FRANK H. DRIGGS. JOHN W. MARDEN..
US309682A 1928-10-01 1928-10-01 Method of preparing rare refractory metals Expired - Lifetime US1821176A (en)

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Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2519792A (en) * 1942-04-10 1950-08-22 Rosen Raphael Electrolytic production of metallic uranium
US2690421A (en) * 1943-03-06 1954-09-28 William C Lilliendahl Electrolytic production of uranium powder
US2714575A (en) * 1952-07-03 1955-08-02 Horizons Titanium Corp Production of metallic titanium
US2715093A (en) * 1952-01-25 1955-08-09 Senderoff Seymour Electrolytic production of molybdenum powder and coherent deposits
US2749295A (en) * 1951-10-18 1956-06-05 Nat Lead Co Electrolytic production of titanium
US2774729A (en) * 1944-01-31 1956-12-18 Meister George Recovery of uranium by electrolysis of a fused bath
US2777809A (en) * 1948-03-25 1957-01-15 Kolodney Morris Preparation of uranium
US2893928A (en) * 1948-04-28 1959-07-07 Kolodney Morris Preparation of plutonium
US2946699A (en) * 1947-03-24 1960-07-26 Manuel C Sanz Process of impregnating graphite with a uranium compound
US2951794A (en) * 1958-05-12 1960-09-06 Chicago Dev Corp Pure chromium
US2960451A (en) * 1959-02-25 1960-11-15 Harvey L Slatin Electrolytic production of refractory multivalent metals
US3114682A (en) * 1962-03-13 1963-12-17 Frederick A Scott Method of preparing chromium dioxide
US3470073A (en) * 1967-10-25 1969-09-30 Nippon Kokan Kk Method of electroplating aluminum

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2519792A (en) * 1942-04-10 1950-08-22 Rosen Raphael Electrolytic production of metallic uranium
US2690421A (en) * 1943-03-06 1954-09-28 William C Lilliendahl Electrolytic production of uranium powder
US2774729A (en) * 1944-01-31 1956-12-18 Meister George Recovery of uranium by electrolysis of a fused bath
US2946699A (en) * 1947-03-24 1960-07-26 Manuel C Sanz Process of impregnating graphite with a uranium compound
US2777809A (en) * 1948-03-25 1957-01-15 Kolodney Morris Preparation of uranium
US2893928A (en) * 1948-04-28 1959-07-07 Kolodney Morris Preparation of plutonium
US2749295A (en) * 1951-10-18 1956-06-05 Nat Lead Co Electrolytic production of titanium
US2715093A (en) * 1952-01-25 1955-08-09 Senderoff Seymour Electrolytic production of molybdenum powder and coherent deposits
US2714575A (en) * 1952-07-03 1955-08-02 Horizons Titanium Corp Production of metallic titanium
US2951794A (en) * 1958-05-12 1960-09-06 Chicago Dev Corp Pure chromium
US2960451A (en) * 1959-02-25 1960-11-15 Harvey L Slatin Electrolytic production of refractory multivalent metals
US3114682A (en) * 1962-03-13 1963-12-17 Frederick A Scott Method of preparing chromium dioxide
US3470073A (en) * 1967-10-25 1969-09-30 Nippon Kokan Kk Method of electroplating aluminum

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