US765001A - Process of manufacturing vanadium and its alloys. - Google Patents

Process of manufacturing vanadium and its alloys. Download PDF

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US765001A
US765001A US15642603A US1903156426A US765001A US 765001 A US765001 A US 765001A US 15642603 A US15642603 A US 15642603A US 1903156426 A US1903156426 A US 1903156426A US 765001 A US765001 A US 765001A
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vanadium
alloys
bath
carbon
fluorid
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Gustave Gin
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    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/244Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing sulfur or phosphorus
    • D06M13/282Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing sulfur or phosphorus with compounds containing phosphorus
    • D06M13/292Mono-, di- or triesters of phosphoric or phosphorous acids; Salts thereof
    • D06M13/295Mono-, di- or triesters of phosphoric or phosphorous acids; Salts thereof containing polyglycol moieties; containing neopentyl moieties

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  • the object of my process is the manufacture of vanadium and-of its alloys by the electrolytic method.
  • the trioxid of vanadium prepared by the known process consisting in calcining the vanadic acid in presence of carbon, is mixed with a suitable proportion of finely-powdered retort-coke or petroleum-coke. Then an addition of hot tar is made in a quantity sufficient to obtain by malaxating a homogeneous and After being malaxated in a special kneadingtrough outwardly heated the paste passes into a mill, wherein it is crushed by very heavy steel rollers.
  • paste on leaving the mill is pounded under stamps and then forced by hydraulic pressure into a drawplate apparatus similar to those used for the manufacture of carbon electrodes.
  • electrodes are manufactured by the direct agglomeration of vanadic acid or of tetroxid of vanadium, which passes at a high temperature and in the presence of carbon to the state of trioxid; but owing to the elimination of oxygen and of carbon resulting from the use of superior oxids porous products are obtained less dense and the electric resisting power whereof is more considerable.
  • the cathodic section should be appreciably less than the active surface of the anodes.
  • a good result and a sufficiently liquid bath are obtained with a medium density of two amperes per square centimeter of active surface of the anodes and of six amperes per square centimeter of section of the cathode, the voltage being between eleven and twelve volts.
  • the ferric fluorid introduced into the bath at the commencement of the operation only serves to set going the dissolution of the anode and the electrolysis of the vanadium.
  • the process for the electrical manufacture of vanadium alloys which consists in subjecting an anode made of an agglomerated mixture'of carbon and vanadium oxid to electrolytic action in a fused bath consisting of calcium fluorid and a fiuorid of the metal with which the metal is to be alloyed, introducing the metal with which the vanadium is to be alloyed, in a metallic state in proximity of the cathode, and tapping the resultant alloy product.

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  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Manufacture And Refinement Of Metals (AREA)
  • Electrolytic Production Of Metals (AREA)

Description

No. 765,001. PATENTBD JULY 12, 1904.
G. GIN. PROCESS 01 MANUFACTURING VANADIUM AND ITS ALLOYS.
APPLICATION FILED MAY 9, 1903 HO IODEL.
UNITED STATES Patented July 12, 1904:.
PATENT OFFICE.
GUSTAVE GIN, OF'PARIS, FRANCE.
SPECIFICATION forming part of Letters Patent N 0,
765,001, dated July 12, 1904.
Application filed May 9, 1903. Serial No. 156/3526. (No specimens.)
To all whom, it may concern.-
Be it known that I, GUsTAvE GIN, a citizen of the French Republic, and a resident of Paris, France, have invented a certain new Process for the Manufacture of Vanadium and Its Alloys, of which the following is a specification.
The object of my process is the manufacture of vanadium and-of its alloys by the electrolytic method.
The principle of my process rests upon the great conductibility of the trioxid of vanadium and upon the facility with which the trifluorid of vanadium is obtained by treating the trioxid with fluorin in presence of carbon. In order to show how these characteristic properties can be utilized to produce ferro-vanadium, for instance, let itvbe sup posed that sesquifluorid of iron dissolved in melted fluorid of calcium be electrolyzed by using an anode formed by an intimately-agglomerated mixture of trioxid of vanadium and of carbon, the cathode being constituted by a bath of metallic iron. The ferric fluorid being decomposed by the current, the fiuorin freed at the contact of the anode attacks the trioxid of vanadium, which yields its oxygen to the carbon, While trifiuorld of vanadium is formed according to the following reactions:
ater The fluorid of vanadium formed enters into solution in the fiuorid of calcium and in its turn is electrolyzed.
lihl il plastic paste.
operation and to furnish the fluorin, servingas a means of transport to cause the vanadium to pass from the anode to the cathode.
It is evident that my process is applicable under similar conditions to the industrial manufacture of alloys of vanadium with other metals, such as copper, aluminium, manganese, &c. It will be suflicient to replace the cathodic bath of iron by a bath of the metal which must come in the alloy.
Having set forth the principle of my invention, I will now proceed to explain how I act in practice.
The trioxid of vanadium prepared by the known process, consisting in calcining the vanadic acid in presence of carbon, is mixed with a suitable proportion of finely-powdered retort-coke or petroleum-coke. Then an addition of hot tar is made in a quantity sufficient to obtain by malaxating a homogeneous and After being malaxated in a special kneadingtrough outwardly heated the paste passes into a mill, wherein it is crushed by very heavy steel rollers. The
paste on leaving the mill is pounded under stamps and then forced by hydraulic pressure into a drawplate apparatus similar to those used for the manufacture of carbon electrodes.
Finally, prismatic or cylindrical blocks are obtained, which are baked, safe from contact with the air, in furnaces of a high temperature. The electrodes thus manufactured until required for use are kept beneath a layer of a dry pulverulent material, so as to thor oughly protect them from contact with the air. It is evident that the electrodes can be manufactured by the direct agglomeration of vanadic acid or of tetroxid of vanadium, Which passes at a high temperature and in the presence of carbon to the state of trioxid; but owing to the elimination of oxygen and of carbon resulting from the use of superior oxids porous products are obtained less dense and the electric resisting power whereof is more considerable.
In order that the operation may be better understood, I annex to this specification a drawing of an electrical furnace (shown in section) which may be used in carrying out my process, although I do not claim any of the features shown in said drawing.
There is a multiple anode E and a watercooled metallic cathode A. The lining of the crucible Q is such that it cannot be attacked by the ingredients of the bath. During the operation the bottom of the crucible is lilled with a molten bath B of the metal with which the vanadium-is to be alloyed, if an alloy is desired. The upper portion of the crucible is filled with a bath C, calcium fluorid in fusion. hen the apparatus is ready to work, the fluorid of vanadium or the liuorid of the metal with which the vanadium is to be alloyed is introduced in the calcium-fluorid bath and the operation takes place according to the reactions mentioned above. For alloys having more than twenty-live per cent. of vanadium the cathodic section should be appreciably less than the active surface of the anodes. A good result and a sufficiently liquid bath are obtained with a medium density of two amperes per square centimeter of active surface of the anodes and of six amperes per square centimeter of section of the cathode, the voltage being between eleven and twelve volts. As I said at the beginning, the ferric fluorid introduced into the bath at the commencement of the operation only serves to set going the dissolution of the anode and the electrolysis of the vanadium. However, as there is a loss of a certain quantity of fluorin transformed into gaseous tetrafluorid of carbon upon contact with the carbon in excess in the mixture forming the anode it is desirable to compensate that loss by adding to the bath from time to time a certain proportion of ferric fluorid. The iron constituting the cathodic bath is introduced in a metallic state and in small quantities at a time after each tapping of ferrovanadium. If no iron be introduced in the bath, almost pure vanadium may be obtained, which is very difficult to tap in a liquid state and must be extracted from the furnace in a solid state.
Having now fully described my said invention, what I claim, and desire to secure by Letters Patent, is
The process for the electrical manufacture of vanadium alloys which consists in subjecting an anode made of an agglomerated mixture'of carbon and vanadium oxid to electrolytic action in a fused bath consisting of calcium fluorid and a fiuorid of the metal with which the metal is to be alloyed, introducing the metal with which the vanadium is to be alloyed, in a metallic state in proximity of the cathode, and tapping the resultant alloy product.
In testimony whereof I have hereunto set my hand in presence of two Witnesses.
GUSTAVE GIN.
WVitnesses:
ADoLrrm S'IURM, J. ALLIsoN BOWEN.
US15642603A 1903-05-09 1903-05-09 Process of manufacturing vanadium and its alloys. Expired - Lifetime US765001A (en)

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Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2934486A (en) * 1957-05-31 1960-04-26 Du Pont Anode structure
US3038852A (en) * 1958-09-29 1962-06-12 Meuter Ernst Device for the galvanization of the bearing surfaces of heavy and very heavy crank shafts
US3130140A (en) * 1960-09-02 1964-04-21 Anocut Eng Co Electrolytic cavity sinking apparatus
US3502553A (en) * 1965-02-16 1970-03-24 Hans Gruber Process and apparatus for the electrolytic continuous direct production of refined aluminum and of aluminum alloys
US3544443A (en) * 1967-02-20 1970-12-01 Evgeny Ivanovich Adaev Device for the installation of the cathode dome with diaphragm into the electrolytic cell
US4409083A (en) * 1980-02-06 1983-10-11 Metallurgical, Inc. Cell with composite anode for electrolytic production of magnesium
US5185068A (en) * 1991-05-09 1993-02-09 Massachusetts Institute Of Technology Electrolytic production of metals using consumable anodes

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2934486A (en) * 1957-05-31 1960-04-26 Du Pont Anode structure
US3038852A (en) * 1958-09-29 1962-06-12 Meuter Ernst Device for the galvanization of the bearing surfaces of heavy and very heavy crank shafts
US3130140A (en) * 1960-09-02 1964-04-21 Anocut Eng Co Electrolytic cavity sinking apparatus
US3502553A (en) * 1965-02-16 1970-03-24 Hans Gruber Process and apparatus for the electrolytic continuous direct production of refined aluminum and of aluminum alloys
US3544443A (en) * 1967-02-20 1970-12-01 Evgeny Ivanovich Adaev Device for the installation of the cathode dome with diaphragm into the electrolytic cell
US4409083A (en) * 1980-02-06 1983-10-11 Metallurgical, Inc. Cell with composite anode for electrolytic production of magnesium
US5185068A (en) * 1991-05-09 1993-02-09 Massachusetts Institute Of Technology Electrolytic production of metals using consumable anodes

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