US410568A - Process of producing aluminium - Google Patents
Process of producing aluminium Download PDFInfo
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- US410568A US410568A US410568DA US410568A US 410568 A US410568 A US 410568A US 410568D A US410568D A US 410568DA US 410568 A US410568 A US 410568A
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- aluminum
- fluoride
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- fused
- aluminous
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- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 title description 23
- 229910052782 aluminium Inorganic materials 0.000 title description 22
- 238000000034 method Methods 0.000 title description 15
- 230000008569 process Effects 0.000 title description 14
- 239000004411 aluminium Substances 0.000 title description 3
- 239000003153 chemical reaction reagent Substances 0.000 description 18
- 229910052751 metal Inorganic materials 0.000 description 14
- 239000002184 metal Substances 0.000 description 14
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 11
- 239000000463 material Substances 0.000 description 10
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 150000002222 fluorine compounds Chemical class 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000010703 silicon Substances 0.000 description 4
- 229910052710 silicon Inorganic materials 0.000 description 4
- DWFFKGPZNGKUPH-UHFFFAOYSA-N sulfanylidenesilicon Chemical compound S=[Si] DWFFKGPZNGKUPH-UHFFFAOYSA-N 0.000 description 4
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 229910052731 fluorine Inorganic materials 0.000 description 3
- 239000011737 fluorine Substances 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 239000005864 Sulphur Substances 0.000 description 2
- 229910052796 boron Inorganic materials 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- 150000004678 hydrides Chemical class 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- ABTOQLMXBSRXSM-UHFFFAOYSA-N silicon tetrafluoride Chemical compound F[Si](F)(F)F ABTOQLMXBSRXSM-UHFFFAOYSA-N 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 150000004763 sulfides Chemical class 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical group F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- 240000006365 Vitis vinifera Species 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 229910002090 carbon oxide Inorganic materials 0.000 description 1
- 239000013065 commercial product Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 229910001610 cryolite Inorganic materials 0.000 description 1
- 230000007717 exclusion Effects 0.000 description 1
- 230000004907 flux Effects 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 239000003517 fume Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000011946 reduction process Methods 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
- GRVFOGOEDUUMBP-UHFFFAOYSA-N sodium sulfide (anhydrous) Chemical compound [Na+].[Na+].[S-2] GRVFOGOEDUUMBP-UHFFFAOYSA-N 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B21/00—Obtaining aluminium
- C22B21/0038—Obtaining aluminium by other processes
- C22B21/0046—Obtaining aluminium by other processes from aluminium halides
Definitions
- MARTIN XVANNER OF ROBINSON, ASSIGNOR OF ONE-HALF TO JOHN A. HALL, OF AXIAL, AND ALBERT H. IVEBER, OF DENVER, COLORADO.
- My invention relates to a new and useful process for the production of metallic aluminum, either in condition sufficiently pure for ordinary uses or as alloyed with any desired metal or metals.
- Its object is to furnish for such production a simple, readily and easily practiced, efficient, and reliable method, one adapted to produce the metal aluminum from aluminous ores, as a commercial product, so economically as to warrant its practical use in many relations in the arts and manufactures Where now cheaper metals not possessing its merits, advantages, and adaptabilities are used.
- my invention consists in a process of treating any of the aluminous fluorides while fused with a compound readily disassociating at a temperature below the fusing-point of the aluminous fluoride, and having an element or elements of such high affinity for fluorine that it or they at the moment of disassociation, or while 5mm )ZCLSCG'IMM, unite immediately with such element or elements of the aluminous fluorides as are in combination with the aluminum, displacing and leaving the latter free, a process for the production of the metal by substitution, as it may be termed, as hereinafter described and claimed.
- the aluminous base used may be the ordinary fluoride of aluminum, either that found as a natural product-such as fluolite-or that formed from the oxide or hydroxide or other aluminous compound, or such base may be a double fluoride of aluminum and an alkaline metal such as cryolite or Al Fl flNaFl.
- ⁇ Vhile either may be used as the base, it is preferable to mix them and use as the base a mixture of one part of the single fluoride to two parts of the double fluoride of aluminum and an alkaline metal, for the reason that the sodium or other alkaline metal in the double fluoride forms a suitable fluxing material, enabling the reduction process to be carried on with out the addition of extraneous fluxes, While in such compound the other elements are present in the combining proportions proper for the reagents to be used, as hereinafter speci fied.
- the base used is fed into or placed within any suitable furnace or crucible containinga bath of fused metal, and is then itself fused upon or over such bath or in such relation thereto that the fused material may flow into or upon such bath.
- the base thus fused and in the bath is then treated with a reagent Whose elements disassociatevat a temperature lower than that of the fused base, and having an element of greater afiinity for fluorine than has the aluminum.
- reagents are the sulphides of silicon and of boron and the hydrides of the same and the carbo-hydrides thereof.
- the mode of the application of these reagents Will vary somewhat with the furnace or crucible used and the particular reagent employed.
- the application may be by passing the reagent through the fused mass in a gaseous state, when it assumes or can be made to assume such state,
- the reagent While containing oxygen, does not part therewith to or in the presence of the other elementsas carbon monoxide, for instanceor the reagent may have been mingled With the aluminous fluoride while the latter was still in a solid state, the essential thing being 0 that the aluminous base and the reagent should be in relation to each other for the operation of their affinities and changes of combination at the moment of disassociation of the elements of the reagent. In the reactions that follow all the original combinations are broken up, and the elements, excepting aluminum, enter into new ones, the aluminum being replaced in its former combinations by other elements and left in afree metallic state.
- the freed aluminum should be protected from contact with air or other oxygen-yielding material. While in the bath the slag formed, in part at least, of the sodium from the double fluoride does this, but it is also preferable that the process should be carried on in a furnace from which air is excluded as thoroughly as possible.
- the metallic bath referred to should be of fused aluminum. Otherwise it should be of such metal as it is desired to alloy the aluminum with.
- Figure 1 is a section of such furnace on the line 00 as, Fig. 3; Fig. 2, a
- FIG. 3 an end elevation thereof.
- reference-numeral 1 indicates the chamber of the furnace, from which, over a bridge-wall 3, leads a flue 4 to the flue 2, the latter being connected to any suitable stack or chimney-pipe.
- the front of the chamber is a depression 5, forming a crucible or pot, the floor 6 of the remainder of the base of the chamber sloping thereto and draining thereinto.
- a tuyere 7 leads into such crucible 5, while therefrom proceeds the draw-off passage 8.
- a water-jacketed inlet 9 for the material to be treated, the inlet being so situated that the material shall fall therethrough upon the upper end of sloping floor 6.
- a fuel-inlet. is arranged at 10 for the admission of the gaseous fuel-as mingled air and hydrocarbon, oxyhydrogen, &c.intended to be used.
- a peep-hole 11 is arranged, having its outer limit covered w1th glass to shut out access of air thereby to the interior of the furnace.
- the retorts being so located that the heat of the waste and escaping products of combustion may be utilized for such prepaof material is stopped.
- retorts 12 are connected at their rears by a pipe 16, that the vapors arising may freely pass from one to another.
- a pipe 17 is arranged to connect with the tuyere 7, so that if the reagent is in gaseous form, and it is so desired, the reagent may be passed directlyfrom the retorts to the interior of the furnace.
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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
(No Model.)
M. WANNER.
PROCESS OF PRODUCING ALUMINIUM.
No. 410,568. Patented Sept. 3, 1889.
8 l/Vl/E/VTOR 12 77mm mm 18 0% 3C "4,;
ATTORNEY UNITED STATE s PATENT OFFICE.
MARTIN XVANNER, OF ROBINSON, ASSIGNOR OF ONE-HALF TO JOHN A. HALL, OF AXIAL, AND ALBERT H. IVEBER, OF DENVER, COLORADO.
PROCESS OF PRODUCING ALUMINIUM.
SPECIFICATION forming part of Letters Patent No. 410.568, dated September 3, 1889.
Application filed August 8, 1888- Serial No. 282,236. (No specimens.)
To all whom it may concern:
Be it known that I, MARTIN \VANNER, a citizen of'the United States of America, residing at Robinson, in the county of Summit and State of Colorado, have invented a certain new and useful Process of Producing Aluminum, of which the following is a specification, reference being had therein to the accompanying drawings.
My invention relates to a new and useful process for the production of metallic aluminum, either in condition sufficiently pure for ordinary uses or as alloyed with any desired metal or metals.
Its object is to furnish for such production a simple, readily and easily practiced, efficient, and reliable method, one adapted to produce the metal aluminum from aluminous ores, as a commercial product, so economically as to warrant its practical use in many relations in the arts and manufactures Where now cheaper metals not possessing its merits, advantages, and adaptabilities are used.
To these ends my invention consists in a process of treating any of the aluminous fluorides while fused with a compound readily disassociating at a temperature below the fusing-point of the aluminous fluoride, and having an element or elements of such high affinity for fluorine that it or they at the moment of disassociation, or while 5mm )ZCLSCG'IMM, unite immediately with such element or elements of the aluminous fluorides as are in combination with the aluminum, displacing and leaving the latter free, a process for the production of the metal by substitution, as it may be termed, as hereinafter described and claimed.
In practicing my process the aluminous base used may be the ordinary fluoride of aluminum, either that found as a natural product-such as fluolite-or that formed from the oxide or hydroxide or other aluminous compound, or such base may be a double fluoride of aluminum and an alkaline metal such as cryolite or Al Fl flNaFl. \Vhile either may be used as the base, it is preferable to mix them and use as the base a mixture of one part of the single fluoride to two parts of the double fluoride of aluminum and an alkaline metal, for the reason that the sodium or other alkaline metal in the double fluoride forms a suitable fluxing material, enabling the reduction process to be carried on with out the addition of extraneous fluxes, While in such compound the other elements are present in the combining proportions proper for the reagents to be used, as hereinafter speci fied.
The base used is fed into or placed Within any suitable furnace or crucible containinga bath of fused metal, and is then itself fused upon or over such bath or in such relation thereto that the fused material may flow into or upon such bath. The base thus fused and in the bath is then treated with a reagent Whose elements disassociatevat a temperature lower than that of the fused base, and having an element of greater afiinity for fluorine than has the aluminum. Among such reagents are the sulphides of silicon and of boron and the hydrides of the same and the carbo-hydrides thereof. The mode of the application of these reagents Will vary somewhat with the furnace or crucible used and the particular reagent employed. The application may be by passing the reagent through the fused mass in a gaseous state, when it assumes or can be made to assume such state,
While containing oxygen, does not part therewith to or in the presence of the other elementsas carbon monoxide, for instanceor the reagent may have been mingled With the aluminous fluoride while the latter Was still in a solid state, the essential thing being 0 that the aluminous base and the reagent should be in relation to each other for the operation of their affinities and changes of combination at the moment of disassociation of the elements of the reagent. In the reactions that follow all the original combinations are broken up, and the elements, excepting aluminum, enter into new ones, the aluminum being replaced in its former combinations by other elements and left in afree metallic state. For instance, if silicon sulphide were the reagent employed, its silicon IOO at the moment of disassociation attacks the fluorine 'and combines therewith, to the exclusion of the aluminum, there being as re-f sultants, besides other elements or compounds, silicon fluoride and free aluminum, the silicon being substituted for the aluminum in the fluorine compounds. The same reaction and results follow the use of either of the sulphides, hydrides, or carbo-hydrides of silicon or boron, they being generic equivalents in the processnoted.
While in the fused condition the freed aluminum should be protected from contact with air or other oxygen-yielding material. While in the bath the slag formed, in part at least, of the sodium from the double fluoride does this, but it is also preferable that the process should be carried on in a furnace from which air is excluded as thoroughly as possible.
When it is desired to obtain the aluminum in a practically or commercially pure state, the metallic bath referred to should be of fused aluminum. Otherwise it should be of such metal as it is desired to alloy the aluminum with.
As giving a practical illustration of the use of. this process, I will now describe it as carried on with the furnace illustrated in the accompanying drawingsa furnace which I have designed with especial reference to the needs of this process, and for which I have made a separate application for Letters Patent contemporaneous herewith.
In such drawings, Figure 1 is a section of such furnace on the line 00 as, Fig. 3; Fig. 2, a
front elevation thereof; Fig. 3, an end elevation thereof.
In these figures the reference-numeral 1 indicates the chamber of the furnace, from which, over a bridge-wall 3, leads a flue 4 to the flue 2, the latter being connected to any suitable stack or chimney-pipe.
In the base of what may be termed the front of the chamber is a depression 5, forming a crucible or pot, the floor 6 of the remainder of the base of the chamber sloping thereto and draining thereinto. A tuyere 7 leads into such crucible 5, while therefrom proceeds the draw-off passage 8.
In the top of the chamber is arranged a water-jacketed inlet 9, for the material to be treated, the inlet being so situated that the material shall fall therethrough upon the upper end of sloping floor 6. A fuel-inlet.is arranged at 10 for the admission of the gaseous fuel-as mingled air and hydrocarbon, oxyhydrogen, &c.intended to be used.
In order that the condition of the material under treatment maybe noted, a peep-hole 11 is arranged, having its outer limit covered w1th glass to shut out access of air thereby to the interior of the furnace.
In the flue 2 are located one or more rebe used, the retorts being so located that the heat of the waste and escaping products of combustion may be utilized for such prepaof material is stopped.
ration. If two or more retorts 12 are used, they are connected at their rears by a pipe 16, that the vapors arising may freely pass from one to another. From the upper part of the lower retort a pipe 17 is arranged to connect with the tuyere 7, so that if the reagent is in gaseous form, and it is so desired, the reagent may be passed directlyfrom the retorts to the interior of the furnace.
It is to be understood that all the pipes herein noted may be provided with suitable dampers or valves, so'that their action may be permit-ted or interdicted, as may by desirable. 7
Into the upper retort leads a pipe 15, by
I which sulphur or other necessary vapors or gases may be passed thereinto, while from the lower part of the front of the lower retort leads a pipe 18. As when the retorts are used to prepare the reagents used, such may be prepared more rapidly than they are consumed, this pipe 18 may lead to any convenient tank or receptacle for the reception and storage of the surplus or prepared reagents.
Supposing now a mixture of fluoride and a double fluoride, as noted, is to be used as the aluminum-yielding material and silicon sulphide .as the reagent; the metallic bath in kettle or crucible 5 is made ready, filling the kettle to about the tuyere-line, and the material to be reduced is introduced through the feed-hole 9 upon the sloping floor 6.' The heat from the gaseous fuel entering through fuel-inlet 1O fuses the material, which flows upon the metal bath in crucible 5, and when such crucible is about full the introduction Thereupon the silicon sulphide is passed into and through the fused mass from the tuyere 7, causing the reactions before noted. Through the peephole 11 the progress of the operation is noted, and when it is seen that no more vapors of silicon fluoride and sodium sulphide rise from the fused mass (which is indicated by the changed color of the rising vapors) the supply of silicon sulphide is cut off, the reduction being then complete. Any foreign matters collect upon the top of the massas scoriae or slagand are drawn off through slag-passage 13, while a portion of the reduced Lmetal is drawn off by spout 8, enough being 'left in the crucible 5 to form the metallic bath for the next charge. In the meantime I a batch of the reagent sulphide has been in i course of preparation in the retorts 12. Therein was placed silicon dioxide and carbon, the same being heated by the products ;of combustion passing around them in the fine 2. pipe 15 the vapors or fumes of sulphur sub- 3 limed in a separate vessel, carbon oxide and l the needed disulphide being the results, as be i fore recited.
Having thus described my invention, what I claim is 1. The process of producing the metal aluminum herein described, consisting in treating a fused aluminous fluoride orfluorides, While in a molten-metallic bath and protected from oxidizing agents, with a reagent Whose elements disassociate at a temperature below the fusing-point of the aluminous fluoride or fluorides, and having an element of such affinities that it displaces the aluminum in the flu- Z. F. WILBER, A. H. WEBER.
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US410568A true US410568A (en) | 1889-09-03 |
Family
ID=2479502
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US410568D Expired - Lifetime US410568A (en) | Process of producing aluminium |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US410568A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3861904A (en) * | 1971-01-04 | 1975-01-21 | Donald F Othmer | Method for producing aluminum metal directly from ore |
-
0
- US US410568D patent/US410568A/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3861904A (en) * | 1971-01-04 | 1975-01-21 | Donald F Othmer | Method for producing aluminum metal directly from ore |
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