US2546548A - Anode for electrowinning manganese and method of making the same - Google Patents

Anode for electrowinning manganese and method of making the same Download PDF

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Publication number
US2546548A
US2546548A US601326A US60132645A US2546548A US 2546548 A US2546548 A US 2546548A US 601326 A US601326 A US 601326A US 60132645 A US60132645 A US 60132645A US 2546548 A US2546548 A US 2546548A
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lead
anode
particles
manganese
electrowinning
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US601326A
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Koster John
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Crimora Res and Dev Corp
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Crimora Res and Dev Corp
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    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25CPROCESSES FOR THE ELECTROLYTIC PRODUCTION, RECOVERY OR REFINING OF METALS; APPARATUS THEREFOR
    • C25C7/00Constructional parts, or assemblies thereof, of cells; Servicing or operating of cells
    • C25C7/02Electrodes; Connections thereof

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  • This invention relates to anodes for the electrowinning of manganese. It has for its object the provision of anodes of lead alloys on which may be formed an adherent coating composed essentially of manganese and lead oxides. This has been accomplished in the past by the use of -certain alloys of lead, such as lead with 1% silver and lead with 1% silver and 1% arsenic. Such alloys are relatively expensive and must be used at relatively high current densities. Furthermore, they require certain preforming before they are eifective in reducing the formation of manganese dioxide at the anode during the electrolytic production of manganese.
  • anode which requires a considerably reduced period of preformin and which can be used over a wider rahgeof. current density and also one which is relativelyinexpensive.
  • Another object is to make anodes composed of elongated particles dispersed in lead alloys more effective by orienting vthe'particles.
  • the anodes of the prior art such as the lead-silver and lead-silverarsenic anodes, have beenv made only by casting hypoeutectic alloys, that is, homogeneous liquid metals which separate crystals of lead and their eutectics.
  • small particles of relatively hard material substantially insoluble in liquid lead are dispersed in liquid lead.
  • the mixture of fine, reatively hard, insoluble particles, and the liquid lead is then allowed to solidify and the solidified mass used as an anode either with or without further shaping.
  • the relatively hard, insoluble particles may be mixed with or imbedded in solid lead .and the solid mixture formed into an anode.
  • the preferred fine particles would be formed of materials having a relatively high mechanical; strength and toughness and also a great resistanceto electrolytic corrosion.
  • the particles may be firmly held in the lead ma: trix, it is also desirable that they be wettedby the lead matrix.
  • the particulate material added to the lead may also be formed in the molten lead itself.
  • nickel and antimony may be separately added to the lead in order to form insoluble particles ofnickel antimonide.
  • tungsten may bedissolved up to 10% in molten lead at 700 C. On cooling, idiomorphic crystals of tungsten will separate. Molybdenum behaves similarly to tungsten.
  • platinum or palladium may be added to lead to form an intermetallic compound therewith which will separate on cooling.
  • the materials which may be added to lead, in accordance with this invention may be divided into four classes: 1. Hard insoluble nonmetallic particles; such as silica, alumina, feldspar and mica.
  • Intermetallic compounds formed by combining the constituents in molten lead such as nickel antimonide, and silver antimonide, and lead platinide.
  • the second class of particles namely, metallic particles
  • This process of tinning may be accomplished by the use of the usual tinning or soldering fluxes, or it may be accomplished by the electrolytic deposition of a thin coating of tin.
  • the particles may be wetted with lead by the addition of a small amount of which are incorporated therein.
  • the processes 7 7 of powder metallurgy are also available for the production of a dispersion 'of line particles of any suitable material in lead; that is to "say, powdered lead and granules of the added material may be pressed into sheet 'form to provide anode plates.
  • dispersions of hard metallic particles in a lead matrix might be made bythe simultaneous spray coating of a suitable anode base with lead It is contemplated that coatings and some metallic materials, such asstainless tion.
  • elongated particles for dispersion-in lead, in accordance with this inven- .tion.
  • elongated particles are used they are preferably arranged so that their long axis is normal to the face of the anode. This may be accomplished in a variety of ways, for example, by castin the face of the anode against a cooled surface.
  • theanode may be .cast in a suitably arranged magnetic field. Particles may also be oriented in .an electrostatic .field.
  • anode for electrowinning manganese the steps of dispersing fine particles of hand, corrosion-resistant, non-metallic material of sizes between 10 mesh and 200 .mesh ina base made substantially of lead; forming said dispersion into suitable shape for use as an anode; and subjecting the anode to preliminary electrolytic treatment in a manganese electrolyte to convert some of the lead on the surfaces into lead oxideand simultaneously depositing manganese dioxide thereon, thereby formin anchored, adherent coatings of said oxides on the surfaces of the anode.
  • a pro-formed anode for electrowinning manganese comprising aplate consisting substantially of lead having partially imbedded therein dispersed, fine granular particles of an inorganic, hard corrosion-resistant, and non-metallic sub stance; and thin coatings of manganese dioxide and lead oxide electro-deposited on and firmly anchored to said plate by said particles.
  • An anode as set forth in claim wherein the plate contains 1% to 10% by volume of the granular particles and wherein the particles are of sizes from ,10 to 200 mesh.

Description

Patented Mar. 27, 1951 ANODE FOR ELECTROWINNING MANGA- NESE AND METHOD OF MAKING THE SAME John Koster, =Crimora, Va., assignor to CrimOra Research & Development Corporation, .Crimora, Va., a corporation of Virginia No. Drawing. Application June 23, 19.45,v I
e l ,326 .4 r
3 Claims. (01. 20446) This invention relates to anodes for the electrowinning of manganese. It has for its object the provision of anodes of lead alloys on which may be formed an adherent coating composed essentially of manganese and lead oxides. This has been accomplished in the past by the use of -certain alloys of lead, such as lead with 1% silver and lead with 1% silver and 1% arsenic. Such alloys are relatively expensive and must be used at relatively high current densities. Furthermore, they require certain preforming before they are eifective in reducing the formation of manganese dioxide at the anode during the electrolytic production of manganese.
It is the purpose of the present invention to provide an anode which requires a considerably reduced period of preformin and which can be used over a wider rahgeof. current density and also one which is relativelyinexpensive. Another object is to make anodes composed of elongated particles dispersed in lead alloys more effective by orienting vthe'particles. The anodes of the prior art, such as the lead-silver and lead-silverarsenic anodes, have beenv made only by casting hypoeutectic alloys, that is, homogeneous liquid metals which separate crystals of lead and their eutectics.
In accordance with this invention, small particles of relatively hard material substantially insoluble in liquid lead are dispersed in liquid lead. The mixture of fine, reatively hard, insoluble particles, and the liquid lead is then allowed to solidify and the solidified mass used as an anode either with or without further shaping. Alternatively, the relatively hard, insoluble particles may be mixed with or imbedded in solid lead .and the solid mixture formed into an anode.
sisting substantiallvof least It is preferred,
however, to use a mixture of the particles with liquid lead, because, in this way, a more uniform mixture can be obtained and the process is likewise less expensive. It is believed that the action of these relatively hard insoluble particles is to provide tentacles, or protrusions, on the surfaces of the anodes as the lead is corroded away. The tentacles hold the coating of manganese and lead oxides to a sufllcient thickness, so that they are effective in protecting the anode itself from corrosion. In accordance with this conception, the preferred fine particles would be formed of materials having a relatively high mechanical; strength and toughness and also a great resistanceto electrolytic corrosion. In order that the particles may be firmly held in the lead ma: trix, it is also desirable that they be wettedby the lead matrix. The particulate material added to the lead may also be formed in the molten lead itself. For example, nickel and antimony may be separately added to the lead in order to form insoluble particles ofnickel antimonide. As another example, tungsten may bedissolved up to 10% in molten lead at 700 C. On cooling, idiomorphic crystals of tungsten will separate. Molybdenum behaves similarly to tungsten. As still another example, platinum or palladium may be added to lead to form an intermetallic compound therewith which will separate on cooling. For convenience of discussion, the materials which may be added to lead, in accordance with this invention, may be divided into four classes: 1. Hard insoluble nonmetallic particles; such as silica, alumina, feldspar and mica.
2. Relatively hard and corrosion-resistant metallic particles, such as chromium, stainless. steel,
.nickel silicide, zirconium, titanium, tantalum,
thorium, cobalt and stellite.
3. Intermetallic compounds formed by combining the constituents in molten lead, such as nickel antimonide, and silver antimonide, and lead platinide.
4. Metals like tungsten and molybdenum, which separate idiomorphically on cooling the lead. In the application of this invention, when using materials of the first class, it is difiicultto obtain a uniform mixing of the particles with the lead. This can. be accomplished best by mix.- ing thefine nonmetallic particles into the molten lead matrix under a vacuum, since the nonmetallic particles are not wetted by lead and tend to r etain an envelope of air.
In the case of the second class of particles, namely, metallic particles, it is important to bring about the wetting of'these'particle's by the le'ad,"i"n order to insure a more uniform dispersion of particles through the lead, a greater stability of this dispersion and a more firm anchoring of the particles into the lead matrix. In order to bring about this wetting, it is desirable to add certain alloys like tin in a relatively small amount to the lead matrix. It is still more effective to give the particles a very thin coating of tin or tinlead alloy. This process of tinning may be accomplished by the use of the usual tinning or soldering fluxes, or it may be accomplished by the electrolytic deposition of a thin coating of tin. Alternatively, the particles may be wetted with lead by the addition of a small amount of which are incorporated therein. The processes 7 7 of powder metallurgy are also available for the production of a dispersion 'of line particles of any suitable material in lead; that is to "say, powdered lead and granules of the added material may be pressed into sheet 'form to provide anode plates. of such dispersions of hard metallic particles in a lead matrix might be made bythe simultaneous spray coating of a suitable anode base with lead It is contemplated that coatings and some metallic materials, such asstainless tion. However, it is possible to work mechani- .cally many of the dispersions of fine particles in lead which have been .described, even if the dispersed material is brittle. The amount and size of dispersed material which may be used is not jcritical. From 1-10% is a satisfactory amount, the size maybe from LOaZOO-mesh or finer. 1 .Anodes formed inaccordance with this inven- .tion maybe advantageously pretreated so as to provide a surface wherein the hard, relatively insoluble particles protrude from the surface so as 'to'hold the coating which is formed in electrolysis. This .treatmentmay consist of scratch brushing to wear away the softer lead matrix or electrolyticcorrosion to corrode away the lead matrix andleave the particles in relief.
Itis contemplated that certain advantages may I "be gained by using elongated particles for dispersion-in lead, in accordance with this inven- .tion. When such elongated particles are used they are preferably arranged so that their long axis is normal to the face of the anode. This may be accomplished in a variety of ways, for example, by castin the face of the anode against a cooled surface. Also, when the particles are magnetic, theanode may be .cast in a suitably arranged magnetic field. Particles may also be oriented in .an electrostatic .field.
While the invention has been illustrated by theaddition of particles to substantially pure lead, it is contemplated that any corrosion-resistant alloy, composed substantially of lead, may
be used and that the addition of fine particles of material in accordance with this invention will improve its performance as an anode in the electrowinning of manganese.
Obviously the invention is not restricted to the particular forms thereof, herein transscribed, but
is capable of a wide variety of modifications within the scope of the appended claims.
What is claimed is:
.1. In the preparation of an anode for electrowinning manganese, the steps of dispersing fine particles of hand, corrosion-resistant, non-metallic material of sizes between 10 mesh and 200 .mesh ina base made substantially of lead; forming said dispersion into suitable shape for use as an anode; and subjecting the anode to preliminary electrolytic treatment in a manganese electrolyte to convert some of the lead on the surfaces into lead oxideand simultaneously depositing manganese dioxide thereon, thereby formin anchored, adherent coatings of said oxides on the surfaces of the anode.
2. A pro-formed anode for electrowinning manganese, comprising aplate consisting substantially of lead having partially imbedded therein dispersed, fine granular particles of an inorganic, hard corrosion-resistant, and non-metallic sub stance; and thin coatings of manganese dioxide and lead oxide electro-deposited on and firmly anchored to said plate by said particles.
3. An anode, as set forth in claim wherein the plate contains 1% to 10% by volume of the granular particles and wherein the particles are of sizes from ,10 to 200 mesh.
JQHNKOSTER.
REFERENCES CITED The following references are of record in :the file of this patent:
UNITED STATES PATENTS Great Britain Aug. 11. .1921

Claims (1)

1. IN THE PREPARATION OF AN ANODE FOR ELECTROWINNING MANGANESE, THE STEPS OF DISPERSING FINEE PARTICLES OF HAND, CORROSION-RESISTANT, NON-METALLIC MATERIAL OF SIZES BETWEEN 10 MESH AND 200 MESH IN A BASE MADE SUBSTANTIALLY OF LEAD; FORMING SAID DISPERSION INTO SUITABLE SHAPE FOR USE AS AN ANODE; AND SUBJECTING THE ANODE TO PRELIMINARY ELECTROLYTIC TREATMENT IN A MANGANESE ELECTROLYTE TO CONVERT SOME OF THE LEAD ON THE SURFACES INTO LEAD OXIDE AND SIMULTANEOUSLY DEPOSITING MANGANESE DIOXIDE THEREON, THEREBY FORMING ANCHORED, ADHERENT COATINGS OF SAID OXIDES ON THE SURFACES OF THE ANODE.
US601326A 1945-06-23 1945-06-23 Anode for electrowinning manganese and method of making the same Expired - Lifetime US2546548A (en)

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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3108939A (en) * 1958-02-14 1963-10-29 Rolland C Sabins Platinum plug-valve metal anode for cathodic protection
US3206385A (en) * 1960-07-12 1965-09-14 Gen Electric Dispersion hardening
US3284333A (en) * 1962-05-22 1966-11-08 Ionics Stable lead anodes
US4297421A (en) * 1977-11-10 1981-10-27 The International Nickel Co., Inc. Battery and electrolytic cell electrodes

Citations (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US190115A (en) * 1877-05-01 Improvement in dental tools
US224078A (en) * 1880-02-03 Franklih copeland
US539669A (en) * 1895-05-21 And thomas w
US627573A (en) * 1897-12-28 1899-06-27 Charles Cunningham Connor Electrode.
US1119443A (en) * 1912-09-19 1914-12-01 Charles Messick Abrasive plate.
US1276614A (en) * 1918-03-08 1918-08-20 Hermann Beusch Bearing-shell or bearing-box.
GB155810A (en) * 1919-12-22 1921-08-11 Friedrich Mayer Improved grinding tool
GB147685A (en) * 1919-01-09 1921-12-08 Optische Anstalt Goerz Ag Improved manufacture of grinding tools
US2145746A (en) * 1935-05-18 1939-01-31 Tungsten Electrodeposit Corp Anode for electrodeposition of tungsten
US2159982A (en) * 1937-01-05 1939-05-30 Bullock Nettie M Hurd Lead alloy and method of preparing the same
US2320773A (en) * 1940-04-04 1943-06-01 Electro Manganese Corp Electrodeposition of manganese
US2397831A (en) * 1944-05-15 1946-04-02 Harry T Bellamy Production of molded metallic articles

Patent Citations (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US190115A (en) * 1877-05-01 Improvement in dental tools
US224078A (en) * 1880-02-03 Franklih copeland
US539669A (en) * 1895-05-21 And thomas w
US627573A (en) * 1897-12-28 1899-06-27 Charles Cunningham Connor Electrode.
US1119443A (en) * 1912-09-19 1914-12-01 Charles Messick Abrasive plate.
US1276614A (en) * 1918-03-08 1918-08-20 Hermann Beusch Bearing-shell or bearing-box.
GB147685A (en) * 1919-01-09 1921-12-08 Optische Anstalt Goerz Ag Improved manufacture of grinding tools
GB155810A (en) * 1919-12-22 1921-08-11 Friedrich Mayer Improved grinding tool
US2145746A (en) * 1935-05-18 1939-01-31 Tungsten Electrodeposit Corp Anode for electrodeposition of tungsten
US2159982A (en) * 1937-01-05 1939-05-30 Bullock Nettie M Hurd Lead alloy and method of preparing the same
US2320773A (en) * 1940-04-04 1943-06-01 Electro Manganese Corp Electrodeposition of manganese
US2397831A (en) * 1944-05-15 1946-04-02 Harry T Bellamy Production of molded metallic articles

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3108939A (en) * 1958-02-14 1963-10-29 Rolland C Sabins Platinum plug-valve metal anode for cathodic protection
US3206385A (en) * 1960-07-12 1965-09-14 Gen Electric Dispersion hardening
US3284333A (en) * 1962-05-22 1966-11-08 Ionics Stable lead anodes
US3440149A (en) * 1962-05-22 1969-04-22 Ionics Stable lead anodes
US4297421A (en) * 1977-11-10 1981-10-27 The International Nickel Co., Inc. Battery and electrolytic cell electrodes

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