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US1835025A - Method of preparing rare refractory metals by electrolysis - Google Patents

Method of preparing rare refractory metals by electrolysis Download PDF

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Publication number
US1835025A
US1835025A US441711A US44171130A US1835025A US 1835025 A US1835025 A US 1835025A US 441711 A US441711 A US 441711A US 44171130 A US44171130 A US 44171130A US 1835025 A US1835025 A US 1835025A
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Prior art keywords
thorium
rare refractory
preparing
refractory metals
metal
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US441711A
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Frank H Driggs
William C Lilliendahl
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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
    • C25C3/26Electrolytic production, recovery or refining of metals by electrolysis of melts of titanium, zirconium, hafnium, tantalum or vanadium
    • 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

Definitions

  • This invention relates to the art of metallurgy and more particularly relates to the art of electro-metallurgy and has for its object the provision of a method of preparing the rare refractory metals thorium, zirconium and the like group elements (group 4 of the periodic table) by the electrolytic dissociation of their compounds in a fused bath.
  • Another object of this invention is to pro vide a suitable fusionmixture for the use in electrolytically preparing thorium, zirconium and the like metals.
  • Another object of this invention is to provide a method of effecting the electrolytic deposition of metals of the thorium, zirconium group upon a cathode of the so-called floating type, in an adherent sponge-like orm.
  • Uranium belongs to another group of elements than tantalum and forms oxygen compounds which are not soluble in ordecomposed by alkali halogen fusion mixtures.
  • the double alkali fluoride compound KUF employed in this process is substantially oxide free, anhydrous and is highly stable and when fused with alkali fluoride compounds does not tend to interact with atmospheric oxygen to form deleterious oxide compounds.
  • Tantalum and the metals of the same family group may be obtained from fusion mixtures, such as set forth in, copending application 27 5,264 above identified.
  • Uranium is preferably prepared from the fusion mixture of application 351,451, above identified.
  • Chromium and other members of the same family group may also be prepared using the fusion mixture such asis set forth in application Serial No. 351,451.
  • thorium for example, a fusion mixture of equal parts potassium chloride (KCl) and sodium chloride (NaCl) is employed.
  • KCl potassium chloride
  • NaCl sodium chloride
  • the melting point of this admixture is well under 750 to 800 0., the limits within which the alkali metal is retained adjacent the cathode as a metal fog in accordance with the invention set forth in copending application Serial No. 351,451 above identified.
  • anhydrous double thorium potassium fluoride having the empirical formula K ThF
  • This compound may be most readily prepared by adding potassium fluoride to i a solution of thorium nitrate.
  • the proportion of the double thorium potassium fluoride salt that may be added to the fusion mixture of alkali chlorides varies between 5% and 25%. It is preferable to add the minimum amount and to add increments of the double compound as the electrolysis proceeds.
  • the cathode is preferably comprised of molybdenum and in its preferred form is comprised of molybdenum strip.
  • the anode may be comprised of carbon and if desired the conhea ers ea tamer for the fusion mixture may he com- Fed oi graphite or carbon and be emooyed as the anode.
  • Cathode-molybdenum strip approximately mil thick by 1 width and a" immersed length.
  • the method of preparing rare refractory metals of group 4 of the periodic table which comprises electrolytically depositing the same from a fused bath comprised of alkali metal halides containing a proportion of a double halide compound of the rare refractory metal.
  • the method of preparing rare refractory metals of group a of the periodic table which comprises electrolytically dissociating a fused doublealka'li metal-rare metal halide compound in a bath comprised substantially of fused alkali metal chloride compounds.
  • the method of preparing thorium which comprises electrolytically depositing the same from a fused bath comprised of alkali metal halides and a. proportion oi? a double halide compound oi thorium.
  • the method of preparing thorium which comprises electrolytically depositing the same from a fused bath comprised of alkali metal chlorides and a proportion of an anhydrous oxide free double fluoride compound or thorium.
  • the method of preparing thorium which comprises electrolytically despositing the same from a fused bath comprised of sodium and potassium chlorides containing a proportion of oxide free double fluoride compound of thorium.
  • the method of preparing thorium which comprises electrolytlcally depositing thorium metalpowder upon a cathode from a fused bath comprised of a mixture of alkali metal chlorides containing a proportion of an oxide free double fluoride compound of thorium, the temperature of said bath being maintained at a temperature of from 600 C. to 800 C.
  • the method of preparing zirconium which comprises electrolytically depositing the same from a fused bath comprised of alkali metal halides and a portion of a double halide compound of zirconium.
  • the method of preparing zirconium which comprises electrolytically depositing the same from a fused bath comprised of alkali metal chloride and a portion of anhydrous oxygen free double fluoride compound of zirconium.
  • the method of preparing zirconium which comprises electrolytically depositing the same from a fused bath comprised of sodium and potassium chloride containing a portion of oxygen free double fluoride compound of zirconium.

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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

Fatented so. 8, 1931 STATES FRANK H. D'RIGGS, OF BLOOIUIELD, AND WILLIAM C. LIL-LIENDAHL, 0F MONTCLAIR,
NEW JERSEY, ASSIGNORS '10 WESTINGHOUSE LAMP COMPANY, A CORPORATION OI PENNSYLVANIA METHOD OF PREPARING RARE REFRACTORY METALS BY ELECTROLYSIS No Drawing.
This invention relates to the art of metallurgy and more particularly relates to the art of electro-metallurgy and has for its object the provision of a method of preparing the rare refractory metals thorium, zirconium and the like group elements (group 4 of the periodic table) by the electrolytic dissociation of their compounds in a fused bath.
Another object of this invention is to pro vide a suitable fusionmixture for the use in electrolytically preparing thorium, zirconium and the like metals.
Another object of this invention is to provide a method of effecting the electrolytic deposition of metals of the thorium, zirconium group upon a cathode of the so-called floating type, in an adherent sponge-like orm.
Other objects and advantages will become apparent as the invention is more fully disclosed.
In copending applications Serial No. 275,264 filed May 4, 1928; 277,096 filed May 11, 1928; 309,682 filed October 1, 1928;
316,624 filed November 1, 1928 and 351,451 filed March 30 1929 by Frank H. Driggs and Frank H. Driggs, et al., there has been disclosed methodswhich have been devised for the electrolytic extraction of the rare refractory metals from fused baths. The present invention is a continuation in part of these prior filed inventions, and the Frank H. Driggs, co-inventor of the present invention, is the same Frank H. Driggs of theapplications above identified. The William C. Lilliendahl, co-inventor of the present invention, is the same co-inventor of application Serial No. 351,451, above identified.
In the applications above identified the various processes and variations in the basic idea originally set forth in applications Serial No. 275,264 and No. 277,096 above identified, in order to adapt the same to the chemical and metallurgical characteristics of the Application filed April 4, 1930. Serial No. 441,711.
different group elements of the rare refracfused alkali halogen bath is disclosed. Specifica'lly the preparation of tantalum is disclosed and to facilitate the deposition process and to make the same continuous in operation increments of tantalum oxide are added to the bath during the electrolysis process. In this instance the tantalum oxide is soluble in and ionizable in the fusion mixture.
In copending application Serial N 0. 277,096 above identified the method of pre paring uranium metal powder by the electrolytic dissociation of fused baths containing a proportion of a double alkali fluoride compound of uranium is disclosed. Uranium belongs to another group of elements than tantalum and forms oxygen compounds which are not soluble in ordecomposed by alkali halogen fusion mixtures. The double alkali fluoride compound KUF employed in this process is substantially oxide free, anhydrous and is highly stable and when fused with alkali fluoride compounds does not tend to interact with atmospheric oxygen to form deleterious oxide compounds.
In copending application Serial No. 309,682 above identified, there is disclosed a method of preparing rare refractory metals by the electrolytic decomposition of a fusion mixture of alkali and alkaline halides having a specific solubility towards the oxide compounds of the rare refractory metal. The invention is specific to the elements of the chromium group and the fusion mixture is comprised specifically of calcium chloride.
In application Serial No. 316,624 a method of effecting an increase in the particle size of the depositing metals in the prior filed applications by adding to the fusion mixture sis a proportion of an alkali metal chloride compound, is set forth.
In application Serial No. 351,451 is disclosed a method of effecting the deposition of the rare refractory metals upon what is known in the art. as a floating cathode by the use of a relatively low melting fusion mixture containing a proportion of an alkali metal halide compound, maintaining the temperature of the'bath during deposition of the mixture to which is added the rare refractory metal compound, must be varied in accordance with the specific chemical and physical properties of the rare refractory metal and the compound from which it is obtained.
Tantalum and the metals of the same family group may be obtained from fusion mixtures, such as set forth in, copending application 27 5,264 above identified. Uranium is preferably prepared from the fusion mixture of application 351,451, above identified. Chromium and other members of the same family group may also be prepared using the fusion mixture such asis set forth in application Serial No. 351,451.
It has been found, however, that the metals thorium, zirconium and the like group elements cannot be prepared using either of these fusion mixtures for the reason that the oxy en compounds of the metals are not solu le in either the fused double fluoride compound of the element or in the fusion mixture of alkali and alkaline earth metal halides. Moreover such oxide compounds are not readily reduced by the alkali metal fog adjacent the cathode when present in the fusion mixture.
It has also been found that the calcium content of the fusion mixture heretofore employed reacts with the fluorine component of the fusion mixture to form high melting fluoride compounds therewith which increase the melting point of the bath materially when accumulated therein an appreciable amount.
Moreover such compounds being relatively insoluble in wamr and acid are not subsequently readily removed from the metal powder during the recovery process, and in the case of zirconium, for example, separation of the calcium fluoride from the metal powder .by gravity means is impractical.
In order to eliminate these objectional features and to facilitate the electrolytic deposition of the rare refractory metals of the thorium and zirconium group (group 4 of the periodic table), we have employed a mixture of alkali halides rather than a mixture of alkali and alkaline earth halides, and add to this admixture a proportion of an anhydrous oxide free rare refractory metal double halide compound, and effect the deposition of the rare refractory metal from the fusion mixture upon a floatin cathode substantially as heretofore disclose \Ve prefer, without being specifically. limited thereto,to employ the double fluoride compounds of the rare refractory metals in the practice of the present invention, for the reason that they may be most readily and conveniently prepared on a commercial basis, and when prepared may be kept indefinitely without substantial deterioration.
In the preparation of thorium, for example, a fusion mixture of equal parts potassium chloride (KCl) and sodium chloride (NaCl) is employed. The melting point of this admixture is well under 750 to 800 0., the limits within which the alkali metal is retained adjacent the cathode as a metal fog in accordance with the invention set forth in copending application Serial No. 351,451 above identified.
To this fusion mixture is added a proportion of an anhydrous double thorium potassium fluoride having the empirical formula K ThF This compound may be most readily prepared by adding potassium fluoride to i a solution of thorium nitrate.
The proportion of the double thorium potassium fluoride salt that may be added to the fusion mixture of alkali chlorides varies between 5% and 25%. It is preferable to add the minimum amount and to add increments of the double compound as the electrolysis proceeds.
It is also preferable to frequently change cathodes as it has been found that in the metals of this class there is apparently a limit as to the thickness of deposit of the sponge metal that may be built up on the cathode. This limit is believed due to the fact that the deposition of the sponge metal is such that the electrical conductivity from one particle to another is relatively poor. As the deposit builds up the resistance increases and the current .efiiciency thereby decreases.
It has been found, for example, that substantially the same weight deposit of thorium is obtained upon a cathode at the end of an hour as was obtained at the end of the first 15 minutes. By inserting a fresh cathode in the cell each 15 minutesfour times the weight of the deposit obtained on a single cathode was obtained.
The cathode is preferably comprised of molybdenum and in its preferred form is comprised of molybdenum strip. The anode may be comprised of carbon and if desired the conhea ers ea tamer for the fusion mixture may he com- Fed oi graphite or carbon and be emooyed as the anode.
A pecific example of the practice of my invention may be set forth as follows:
Fusion mimiwe v Grams laaCi 500 KGL; 500 o- ZC ThF (anhydrous) 60 F used ingraphite crucible approximately 3% inches diameter by 5 inches deep.
Temperature of bath 750 to. 800 C.
Anode the crucible.
Cathode-molybdenum strip approximately mil thick by 1 width and a" immersed length.
Cathode current density approximately 7-8 amperes per square inch.
Voltage across cell approximately 6 volts.
About every minutes a fresh cathode should be inserted and fresh additions of liflhh to replace that deposited out should made. The current efficiency is about 43 cent. The percent yield is about 53 per In the electrolytic preparation of zirconium there is no specific variation from the bath composition or in the method of depositing the metal powder. The fifty-fifty ad- I mixture of sodium and potassium chlorides is employed to which is added between 5% and 25% zirconium potassium fluoride K ZrF The electrolysis of the fused mixture' is conducted similarly to that above set forth for thorium.
Having broadly and specifically set forth the nature and scope of the present invention it is apparent that there may be many departures and variations made from the specific embodiment herein disclosed without departing essentially from the nature and scope of the invention as is set forth in the accompanying claims.
What is claimed is:
1. The method of preparing rare refractory metals of group 4 of the periodic table which comprises electrolytically depositing the same from a fused bath comprised of alkali metal halides containing a proportion of a double halide compound of the rare refractory metal.
2. The method of preparing rare refractory metals of group a of the periodic table which comprises electrolytically dissociating a fused doublealka'li metal-rare metal halide compound in a bath comprised substantially of fused alkali metal chloride compounds.
3. The method of preparing rare refractory metals of the thorium, zirconium class which comprises electrolyzing a fusion mixture comprised of alkali metal chloride compounds containing a proportion of an anwhich comprises electrolyzing a fusion mixture comprised of alkali metal chloride compounds containing a proportion of a double alkali metal-rare metal fluoride.
5. The method of preparing thorium which comprises electrolytically depositing the same from a fused bath comprised of alkali metal halides and a. proportion oi? a double halide compound oi thorium.
6. The method of preparing thorium which comprises electrolytically depositing the same from a fused bath comprised of alkali metal chlorides and a proportion of an anhydrous oxide free double fluoride compound or thorium.
7. The method of preparing thorium which comprises electrolytically despositing the same from a fused bath comprised of sodium and potassium chlorides containing a proportion of oxide free double fluoride compound of thorium.
8. The method of preparing metal powders of rare refractory metals of group 4: of the periodic table which comprises electrolytically deposit-ing the same upon a cathode from a fused bath comprised of alkali metal chlorides containing a proportion of double halide compound of the rare refractory metal.
9. The method of preparing thorium which comprises electrolytlcally depositing thorium metalpowder upon a cathode from a fused bath comprised of a mixture of alkali metal chlorides containing a proportion of an oxide free double fluoride compound of thorium, the temperature of said bath being maintained at a temperature of from 600 C. to 800 C.
10. The method of preparing zirconium which comprises electrolytically depositing the same from a fused bath comprised of alkali metal halides and a portion of a double halide compound of zirconium.
11. The method of preparing zirconium which comprises electrolytically depositing the same from a fused bath comprised of alkali metal chloride and a portion of anhydrous oxygen free double fluoride compound of zirconium.
12. The method of preparing zirconium which comprises electrolytically depositing the same from a fused bath comprised of sodium and potassium chloride containing a portion of oxygen free double fluoride compound of zirconium.
In testimony whereof, we have hereunto subscribed our names this 2nd day of April,
FRANK H. BRIGGS. WILLIAM C. LILLIENDL.
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Cited By (11)

* 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
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
US2731402A (en) * 1952-07-03 1956-01-17 Horizons Titanium Corp Production of metallic titanium
DE1003959B (en) * 1952-07-03 1957-03-07 Horizons Titanium Corp Process for the production of titanium
US2813068A (en) * 1951-12-21 1957-11-12 Horizons Titanium Corp Production of titanium by fused salt electrolysis
DE1060605B (en) * 1952-07-03 1959-07-02 Horizons Titanium Corp Process for the manufacture of substantially pure titanium
DE1077878B (en) * 1952-10-04 1960-03-17 Norton Ges M B H Deutsche Process for the production of zirconium, hafnium or mixtures of these metals by fused-salt electrolysis
DE1078776B (en) * 1953-05-21 1960-03-31 Norton Ges M B H Deutsche Process for the production of thorium, uranium, niobium, tantalum, vanadium, tungsten, molybdenum or chromium by fused-salt electrolysis
US3002906A (en) * 1959-08-04 1961-10-03 Norton Co Process for the extraction of relatively pure thorium
US20090146098A1 (en) * 2007-12-10 2009-06-11 Fu Zhun Precision Industry (Shen Zhen) Co., Ltd. Powder extinguishing agent and method for manufacturing the same

Cited By (11)

* 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
US2813068A (en) * 1951-12-21 1957-11-12 Horizons Titanium Corp Production of titanium by fused salt electrolysis
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
US2731402A (en) * 1952-07-03 1956-01-17 Horizons Titanium Corp Production of metallic titanium
DE1003959B (en) * 1952-07-03 1957-03-07 Horizons Titanium Corp Process for the production of titanium
DE1060605B (en) * 1952-07-03 1959-07-02 Horizons Titanium Corp Process for the manufacture of substantially pure titanium
DE1077878B (en) * 1952-10-04 1960-03-17 Norton Ges M B H Deutsche Process for the production of zirconium, hafnium or mixtures of these metals by fused-salt electrolysis
DE1078776B (en) * 1953-05-21 1960-03-31 Norton Ges M B H Deutsche Process for the production of thorium, uranium, niobium, tantalum, vanadium, tungsten, molybdenum or chromium by fused-salt electrolysis
US3002906A (en) * 1959-08-04 1961-10-03 Norton Co Process for the extraction of relatively pure thorium
US20090146098A1 (en) * 2007-12-10 2009-06-11 Fu Zhun Precision Industry (Shen Zhen) Co., Ltd. Powder extinguishing agent and method for manufacturing the same

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