US2184705A - Refining and producing aluminum - Google Patents

Refining and producing aluminum Download PDF

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US2184705A
US2184705A US295348A US29534839A US2184705A US 2184705 A US2184705 A US 2184705A US 295348 A US295348 A US 295348A US 29534839 A US29534839 A US 29534839A US 2184705 A US2184705 A US 2184705A
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aluminum
mixture
fluoride
temperature
halide
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US295348A
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Charles B Willmore
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Alcoa Corp
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Aluminum Company of America
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    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B21/00Obtaining aluminium
    • C22B21/06Obtaining aluminium refining
    • C22B21/062Obtaining aluminium refining using salt or fluxing agents

Definitions

  • Aluminum as producedby the ordinary commercial processes now in use, or as recovered as secondary metal or scrap, normally contains impurities, the amount and nature of which depend upon the origin of the metal. It is frequently desirable to remove from aluminum these impurities, which usually take the form of other metallic elements such as iron, silicon, copper, titanium, zinc, magnesium, cadmium, lead, and the like. Such methods as have been pro- ,posed for this purpose are quite expensive.
  • the present invention relates to a distillation process of refining aluminum. Such processes have been previously proposed, but have heretofore not been considered commercial because of the high temperatures at which they must be operated. It is therefore the object of this invention to provide adistillationprocess of refining aluminum which is operable at temperatures consistent with inexpensive and commercial apparatus and at a cost less than that of previously proposed processes of this general type.
  • the halides the fluorides are preferred for this purpose, even over other somewhat cheaper halides, because it has been found that the general efliciency of the process is better when fluorides are used.
  • the fluorides the alkaline earth fluorides and the double fluorides containing aluminum are preferred, and aluminum fluoride is a compound which has been found satisfactory.
  • magnesium fluoride is preferred, although in high temperature operation the higher vaporizing temperature of calcium fluoridemay make the use of this compound desirable.
  • the alkali metal double fluorides are regarded as most satisfactory, and of 0 these the sodium aluminum fluorides, such as cryolite or chiolite, have proven the more efficient.
  • the selection of the halide will be governed by 50 considerations of the thermal characteristics of the halide in question and the temperature of operation. H ides which are unstable at the temperature of peration, or which vaporize readily at that or lower temperatures, thus leaving the reaction zon impoverished in halide prior to effective reaction, are usually not desirable in practice.
  • impure aluminum is first put into a finely divided or comminuted state by a ball-milling operation, atomizing, or by other well known methods for producing small particles.
  • the size of the particles depends, tosome extent, on the other conditions hereinafter described, but should be such as to permit an intimate mixture of the particles with the halide used. For most purposes, particles having-a size less than 14 mesh are preferred.
  • the particles are then mixed with a suitable halide and placedin a heating chamber or furnace.
  • the mixture may be loose when placed in the furnace, but it is preferred to briquette the mixture before introducing it into the furnace. This may be done by subjecting it to pressure in a mold, or by employing a binder. Likewise, it is advantageousto sinter the briquettes before placing them in the furnace.
  • the process is carried out in an atmosphere inert to aluminum, under conaluminum across the briquettes during the heating step.
  • a current of hydrogen may be used.
  • The'mixture in the heating chamber is then heated at an elevated temperature.
  • the temperature used varies, depending upon the particular halide employed in the mixture. For example, when aluminum fluoride is used in the mixture, a temperature of between 900 and 1000 C. is satisfactory. When sodium cryolite (NazAlFe) is used, a temperature of between 900 and 1000 C. may be employed. If the halide is magnesium fluoride, the mixture is heated to a temperature of between 900 and 1300 .C. in the heating step.
  • the heating of the mixture may be accomplished by applying heat externally to the portion of the furnace in which the mixture is located, or internal heating means, such as an electric resistor, maybe employed for the purpose.
  • internal heating means such as an electric resistor
  • vapors are evolved which pass to a cool-' ing zone and condense.
  • the condensing zone may constitute a part of the chamber in which the mixture is heated, but remote from the heating zone, or it may be a separate chamber fromwhich the vapors evolved from the mixture are led from the furnace.
  • the material found in the condensing zone or chamber at the end of the heatingstep consists principally of a mixture of the halide and pellets of aluminum.
  • aluminum may be separated from the balance a high efficiency operation, viz.,
  • aluminum fluoride When aluminum fluoride is used, it is preferably mixed with particles of impure aluminum in the proportions of about 3 parts of aluminum fluoride to 1 part of the aluminum by weight.
  • the temperature at which the mixture is heated when aluminum fluoride is employed is between 900 and 1000 C., the exact temperature depending, to some extent, on such factors as the size of the aluminum particles and the speed and economy with which it is desired to have the process proceed. Ordinarily, a heating period of from 1 to 4 hours is used.
  • magnesium fluoride When magnesium fluoride is used as the halide, it is preferably present in the original mixture in the proportions of about 1 parts of magnesiumfluoride to 1 part of impure-aluminum by weight, and the mixture is heated to a temperature of between 900 and 1200 C.
  • the halide employed is cryolite, the most eiiicient proportions are .about 2 parts of cryolite to 1 part of aluminum by weight, and the temperature to which the mixture is heated between 900 and 1000 C.
  • the retort was maintained by the vacuum pump at a residual gas pressure of .7 millimeter of mercury.
  • the retort was opened, and the deposit found at the cooler end of the retort was removed.
  • the deposit consisted principally of a mixture of cryolite and aluminum, the aluminum being present in the form of pellets. Upon separation of the aluminum from the cryolite, the aluminum was found to contain only 0.01 per cent silicon, 0.05 per cent iron, 0.002 per.
  • briquettes composed of a. mixture of magnesium fluoride and aluminum containing 0.15 per cent silicon, 0.36 per cent iron, 0.01 per cent copper, and 0.007 per cent titanium in the proportions of slightly less than 1 parts of magnesium fluoride to 1 part of the impure aluminum by weight were heated in a horizontal retort for 2 hours at 1120 C. and a pressure, of 4 millimeters of mer cury. Upon separation of the pellets of aluminum from the deposit found in the cooler end of the retort, the aluminumwas found to contain 0.01 per cent silicon, 0.01 per cent iron, 0.001 per cent titanium, and only a trace of copper.
  • the process comprising forming a mixture comprising aluminum and a halide, heating said. mixture in an atmosphere effectively inert to aluminum to vaporize therefrom metallic aluminum and halide, condensing the resulting vapors and separating the aluminum from the condensate.
  • the process comprising forming a mixture comprising aluminum and a fluoride, heating said mixture in an atmosphere eflfectively inert to aluminum to vaporize therefrom metallic aluminum and fluoride, condensing the resulting vapors and separating the aluminum from the condensate.
  • the process comprising forming a mixture comprising aluminum and magnesium fluoride. heating said mixture in an atmosphere efiective- 1y inert to aluminum to vaporize therefrom metallic aluminum and fluoride, condensing the resulting vapors and separating the aluminum from the condensate. 5 5. The process comprising forming a mixture comprising aluminum and double fluorides of an alkali metal and aluminum, heating said mixture in an atmosphere efiectively inert to aluminum to vaporize therefrom metallic aluminum and fluoride, condensing the resulting vapors and separating the aluminum from the condensate.
  • the process comprising forming a mixture comprising aluminum and sodium cryolite, heating said mixture in an atmosphere eflectively in- 15 ert to aluminum to vaporize therefrom metallic aluminum and fluoride, condensing the resulting vapors and separating the aluminum from the condensate.

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  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Manufacture And Refinement Of Metals (AREA)

Description

Patented Dec. 26, 1939 UNITED STATES PATENT OFFICE signor to Aluminum ompany of America,
Pittsburgh, Pa., a corporation of Pennsylvania .No Drawing. Application September 18, 1939, Serial No. 295,348
10 Claims.
Aluminum, as producedby the ordinary commercial processes now in use, or as recovered as secondary metal or scrap, normally contains impurities, the amount and nature of which depend upon the origin of the metal. It is frequently desirable to remove from aluminum these impurities, which usually take the form of other metallic elements such as iron, silicon, copper, titanium, zinc, magnesium, cadmium, lead, and the like. Such methods as have been pro- ,posed for this purpose are quite expensive.
The present invention relates to a distillation process of refining aluminum. Such processes have been previously proposed, but have heretofore not been considered commercial because of the high temperatures at which they must be operated. It is therefore the object of this invention to provide adistillationprocess of refining aluminum which is operable at temperatures consistent with inexpensive and commercial apparatus and at a cost less than that of previously proposed processes of this general type.
I have discovered that when halides are mixed with impure aluminum and the mixture heated to elevated temperatures in a heating chamber,
relatively pure aluminum will vaporize at commercially operable temperatures and rates and may thereafter be recovered by condensing the vapors in a suitable condensing chamber. 0f
the halides the fluorides are preferred for this purpose, even over other somewhat cheaper halides, because it has been found that the general efliciency of the process is better when fluorides are used. 0f the fluorides the alkaline earth fluorides and the double fluorides containing aluminum are preferred, and aluminum fluoride is a compound which has been found satisfactory.
Of the alkaline earth fluorides, magnesium fluoride is preferred, although in high temperature operation the higher vaporizing temperature of calcium fluoridemay make the use of this compound desirable. 0f the double fluorides containing aluminum, the alkali metal double fluorides are regarded as most satisfactory, and of 0 these the sodium aluminum fluorides, such as cryolite or chiolite, have proven the more efficient.
The selection of the halide will be governed by 50 considerations of the thermal characteristics of the halide in question and the temperature of operation. H ides which are unstable at the temperature of peration, or which vaporize readily at that or lower temperatures, thus leaving the reaction zon impoverished in halide prior to effective reaction, are usually not desirable in practice.
It would appear, although this surmise is the oretical and my invention is not'limited thereto, that the halide and the available aluminum form some low boiling mixture, compound, or analo- ,at temperatures below which any aluminum would be normally distilled. My invention therefore contemplates not only the refining of metallic aluminum, but also the recovery of aluminum from those aluminum compounds, or mixtures of aluminum compounds and other substances, which produce, in part at least, under the action of heat, available elementary aluminum. I have mentioned aluminum carbide, but mere mixtures of alumina and carbon have likewise given results, as would be expected whenever the mixture of substances is such that aluminum carbide or other easily dissociated aluminum compounds are formed.
In accordance with my refining process, impure aluminum is first put into a finely divided or comminuted state by a ball-milling operation, atomizing, or by other well known methods for producing small particles. The size of the particles depends, tosome extent, on the other conditions hereinafter described, but should be such as to permit an intimate mixture of the particles with the halide used. For most purposes, particles having-a size less than 14 mesh are preferred. The particles are then mixed with a suitable halide and placedin a heating chamber or furnace. The mixture may be loose when placed in the furnace, but it is preferred to briquette the mixture before introducing it into the furnace. This may be done by subjecting it to pressure in a mold, or by employing a binder. Likewise, it is advantageousto sinter the briquettes before placing them in the furnace.
After the mixture has been placed in the heating chamber, the process is carried out in an atmosphere inert to aluminum, under conaluminum across the briquettes during the heating step. For example, a current of hydrogen may be used.
The'mixture in the heating chamber is then heated at an elevated temperature. The temperature used varies, depending upon the particular halide employed in the mixture. For example, when aluminum fluoride is used in the mixture, a temperature of between 900 and 1000 C. is satisfactory. When sodium cryolite (NazAlFe) is used, a temperature of between 900 and 1000 C. may be employed. If the halide is magnesium fluoride, the mixture is heated to a temperature of between 900 and 1300 .C. in the heating step.
The heating of the mixture may be accomplished by applying heat externally to the portion of the furnace in which the mixture is located, or internal heating means, such as an electric resistor, maybe employed for the purpose. When the mixture is heated as above described, vapors are evolved which pass to a cool-' ing zone and condense. The condensing zone may constitute a part of the chamber in which the mixture is heated, but remote from the heating zone, or it may be a separate chamber fromwhich the vapors evolved from the mixture are led from the furnace. The material found in the condensing zone or chamber at the end of the heatingstep consists principally of a mixture of the halide and pellets of aluminum. The
, aluminum may be separated from the balance a high efficiency operation, viz.,
fluoride, magnesium fluoride, and the double fluorides of aluminum and the alkali metals, of which latter cryolite is preferred. When aluminum fluoride is used, it is preferably mixed with particles of impure aluminum in the proportions of about 3 parts of aluminum fluoride to 1 part of the aluminum by weight. The temperature at which the mixture is heated when aluminum fluoride is employed is between 900 and 1000 C., the exact temperature depending, to some extent, on such factors as the size of the aluminum particles and the speed and economy with which it is desired to have the process proceed. Ordinarily, a heating period of from 1 to 4 hours is used.
When magnesium fluoride is used as the halide, it is preferably present in the original mixture in the proportions of about 1 parts of magnesiumfluoride to 1 part of impure-aluminum by weight, and the mixture is heated to a temperature of between 900 and 1200 C. When the halide employed is cryolite, the most eiiicient proportions are .about 2 parts of cryolite to 1 part of aluminum by weight, and the temperature to which the mixture is heated between 900 and 1000 C.
As an example of the operation of my process. aluminum containing 0.16 per cent silicon, 0.31 per cent iron, 0.01 per cent copper, and 0.008 per cent titanium was commi nuted to 28 mesh size. This material was mixed with cryolite in the proportions of 2 parts of cryolite to 1 part of aluminum by weight, and the mixture was briquetted in a mold by applying pressure to it. Briquettes of the mixture were placed in one end of a closed horizontal retort having a vacuum pump attached to the other end thereof. The end of the retort containing the briquettes was then heated to a temperature of 800 C. for a. period of 3 /2 hours. During that time, the retort was maintained by the vacuum pump at a residual gas pressure of .7 millimeter of mercury. At the end of the heating period, the retort was opened, and the deposit found at the cooler end of the retort was removed. The deposit consisted principally of a mixture of cryolite and aluminum, the aluminum being present in the form of pellets. Upon separation of the aluminum from the cryolite, the aluminum was found to contain only 0.01 per cent silicon, 0.05 per cent iron, 0.002 per.
cent titanium, and no copper. Likewise, briquettes composed of a. mixture of magnesium fluoride and aluminum containing 0.15 per cent silicon, 0.36 per cent iron, 0.01 per cent copper, and 0.007 per cent titanium in the proportions of slightly less than 1 parts of magnesium fluoride to 1 part of the impure aluminum by weight were heated in a horizontal retort for 2 hours at 1120 C. and a pressure, of 4 millimeters of mer cury. Upon separation of the pellets of aluminum from the deposit found in the cooler end of the retort, the aluminumwas found to contain 0.01 per cent silicon, 0.01 per cent iron, 0.001 per cent titanium, and only a trace of copper.
Although the process has been described above as involving the use in conjunction with impure aluminum of only one of the halides or double halides mentioned, it is to be understood that the mixture may contain two or more of the halides.
I claim: v s
1. The process comprising forming a mixture comprising aluminum and a halide, heating said. mixture in an atmosphere effectively inert to aluminum to vaporize therefrom metallic aluminum and halide, condensing the resulting vapors and separating the aluminum from the condensate.
2. The process comprising forming a mixture comprising aluminum and a fluoride, heating said mixture in an atmosphere eflfectively inert to aluminum to vaporize therefrom metallic aluminum and fluoride, condensing the resulting vapors and separating the aluminum from the condensate.
3. The process comprising forming a mixture comprising aluminum and aluminum fluoride, heating said mixture in an atmosphere effectively inert to aluminum to vaporize therefrom metallic aluminum and fluoride, condensing the resulting vapors and separating the aluminum from the condensate.
4. The process comprising forming a mixture comprising aluminum and magnesium fluoride. heating said mixture in an atmosphere efiective- 1y inert to aluminum to vaporize therefrom metallic aluminum and fluoride, condensing the resulting vapors and separating the aluminum from the condensate. 5 5. The process comprising forming a mixture comprising aluminum and double fluorides of an alkali metal and aluminum, heating said mixture in an atmosphere efiectively inert to aluminum to vaporize therefrom metallic aluminum and fluoride, condensing the resulting vapors and separating the aluminum from the condensate.
6. The process comprising forming a mixture comprising aluminum and sodium cryolite, heating said mixture in an atmosphere eflectively in- 15 ert to aluminum to vaporize therefrom metallic aluminum and fluoride, condensing the resulting vapors and separating the aluminum from the condensate.
7. The process comprising forming a mixture 20 comprising aluminum and two or more of the fluorides from the class composed of aluminum fluoride, magnesium fluoride, alkali metal dou-' ble fluorides, and the alkaline earth fluorides,
heating said mixture inan atmosphere eflective- 2:; 1y inert to aluminum to vaporize therefrom metallic aluminum and fluoride, condensing the resuiting vapors and separating the aluminum from the condensate.
' 8. The process of forming a mixture comprising a halide and substance which becomes dissociated by heat at the temperature of the process to produce available elementary aluminum, heating said mixture'in an atmosphere eflectively inert to aluminum and at a temperature be-' low the temperature at which aluminum would appreciably distill in the absence of a halide, thereby to vaporize therefrom metallic aluminum and halide, condensing the resulting vapors and separating the aluminum.
9. The process of forming a mixture comprising a fluoride and substance which becomes dissociated by heat at the temperature of the process to produce available elementary aluminum, heat ing said mixture in an atmosphere effectively inertto aluminum and at a temperature below the temperature at which aluminum would appreciably distill in the absence of a fluoride, thereby to vaporize therefrom metallic aluminum and the condensate.
CHARLES B. WILIMORE.
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Cited By (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2470306A (en) * 1946-03-27 1949-05-17 Int Alloys Ltd Process for the production and refining of metals
US2470305A (en) * 1944-04-19 1949-05-17 Int Alloys Ltd Process for the production and refining of aluminium
US2607675A (en) * 1948-09-06 1952-08-19 Int Alloys Ltd Distillation of metals
US2621120A (en) * 1945-09-20 1952-12-09 Ardal Verk As Process of refining aluminum
US2665223A (en) * 1949-12-31 1954-01-05 Nat Res Corp Process for depositing an aluminum film on a substrate by thermal vaporization
US2723911A (en) * 1954-08-04 1955-11-15 Aluminum Lab Ltd Method of separating aluminum from impurities
US2762702A (en) * 1952-09-29 1956-09-11 Kaiser Aluminium Chem Corp Process of distilling metals with halide vapors
US2776884A (en) * 1951-12-19 1957-01-08 Pechiney Prod Chimiques Sa Process for the manufacture of aluminum
DE1119521B (en) * 1958-06-20 1961-12-14 Atomic Energy Commission Process for the enrichment of plutonium and / or uranium in aluminum alloys
DE976700C (en) * 1950-12-18 1964-03-05 David Leon Levi Process for the extraction of aluminum
DE1196046B (en) * 1955-03-28 1965-07-01 Siemens Ag Process for producing a highly pure, crystalline rod from a conductive or semiconductive element
US3391017A (en) * 1963-08-26 1968-07-02 Int Standard Electric Corp Formation of aluminum, gallium, arsenic, and phosphorous binary conatings
US3397056A (en) * 1965-11-15 1968-08-13 Dow Chemical Co Separation of aluminum from impure aluminum sources
US3620716A (en) * 1969-05-27 1971-11-16 Aluminum Co Of America Magnesium removal from aluminum alloy scrap
US3775092A (en) * 1970-11-11 1973-11-27 J Brusakov Method of refining aluminium-silicon alloys
US3784371A (en) * 1971-12-27 1974-01-08 Dow Chemical Co Corrosion resistant frozen wall
US3844771A (en) * 1970-01-06 1974-10-29 Dow Chemical Co Method for condensing metal vapor mixtures
US3849118A (en) * 1967-08-14 1974-11-19 Dow Chemical Co Production of magnesium metal
US3856511A (en) * 1972-03-13 1974-12-24 Ethyl Corp Purification of crude aluminum
US4188207A (en) * 1978-10-23 1980-02-12 Adams Clyde M Jr Aluminum production
US4769068A (en) * 1986-12-24 1988-09-06 Aluminum Company Of America Process for production of aluminum by carbothermic production of alkaline earth metal aluminide and stripping of aluminum from alkaline earth metal aluminide with sulfurous stripping agent
US4769069A (en) * 1986-12-24 1988-09-06 Aluminum Company Of America Process for production of aluminum by carbothermic production of alkaline earth metal aluminide and stripping of aluminum from alkaline earth metal aluminide with halide stripping agent
US9278391B1 (en) * 2012-08-05 2016-03-08 Charles A. Baer Disproportionation production of nano-metal powders and nano-metal oxide powders

Cited By (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2470305A (en) * 1944-04-19 1949-05-17 Int Alloys Ltd Process for the production and refining of aluminium
US2621120A (en) * 1945-09-20 1952-12-09 Ardal Verk As Process of refining aluminum
US2470306A (en) * 1946-03-27 1949-05-17 Int Alloys Ltd Process for the production and refining of metals
US2607675A (en) * 1948-09-06 1952-08-19 Int Alloys Ltd Distillation of metals
US2665223A (en) * 1949-12-31 1954-01-05 Nat Res Corp Process for depositing an aluminum film on a substrate by thermal vaporization
DE976700C (en) * 1950-12-18 1964-03-05 David Leon Levi Process for the extraction of aluminum
US2776884A (en) * 1951-12-19 1957-01-08 Pechiney Prod Chimiques Sa Process for the manufacture of aluminum
US2762702A (en) * 1952-09-29 1956-09-11 Kaiser Aluminium Chem Corp Process of distilling metals with halide vapors
US2723911A (en) * 1954-08-04 1955-11-15 Aluminum Lab Ltd Method of separating aluminum from impurities
DE1196046B (en) * 1955-03-28 1965-07-01 Siemens Ag Process for producing a highly pure, crystalline rod from a conductive or semiconductive element
DE1119521B (en) * 1958-06-20 1961-12-14 Atomic Energy Commission Process for the enrichment of plutonium and / or uranium in aluminum alloys
US3391017A (en) * 1963-08-26 1968-07-02 Int Standard Electric Corp Formation of aluminum, gallium, arsenic, and phosphorous binary conatings
US3397056A (en) * 1965-11-15 1968-08-13 Dow Chemical Co Separation of aluminum from impure aluminum sources
US3849118A (en) * 1967-08-14 1974-11-19 Dow Chemical Co Production of magnesium metal
US3620716A (en) * 1969-05-27 1971-11-16 Aluminum Co Of America Magnesium removal from aluminum alloy scrap
US3844771A (en) * 1970-01-06 1974-10-29 Dow Chemical Co Method for condensing metal vapor mixtures
US3775092A (en) * 1970-11-11 1973-11-27 J Brusakov Method of refining aluminium-silicon alloys
US3784371A (en) * 1971-12-27 1974-01-08 Dow Chemical Co Corrosion resistant frozen wall
US3856511A (en) * 1972-03-13 1974-12-24 Ethyl Corp Purification of crude aluminum
US4188207A (en) * 1978-10-23 1980-02-12 Adams Clyde M Jr Aluminum production
US4769068A (en) * 1986-12-24 1988-09-06 Aluminum Company Of America Process for production of aluminum by carbothermic production of alkaline earth metal aluminide and stripping of aluminum from alkaline earth metal aluminide with sulfurous stripping agent
US4769069A (en) * 1986-12-24 1988-09-06 Aluminum Company Of America Process for production of aluminum by carbothermic production of alkaline earth metal aluminide and stripping of aluminum from alkaline earth metal aluminide with halide stripping agent
US9278391B1 (en) * 2012-08-05 2016-03-08 Charles A. Baer Disproportionation production of nano-metal powders and nano-metal oxide powders

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