US420945A - Process of reducing metallic oxides to the metallic state - Google Patents
Process of reducing metallic oxides to the metallic state Download PDFInfo
- Publication number
- US420945A US420945A US420945DA US420945A US 420945 A US420945 A US 420945A US 420945D A US420945D A US 420945DA US 420945 A US420945 A US 420945A
- Authority
- US
- United States
- Prior art keywords
- metallic
- reducing
- oxides
- state
- hydrocarbon
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 238000000034 method Methods 0.000 title description 14
- 229910044991 metal oxide Inorganic materials 0.000 title description 8
- OKTJSMMVPCPJKN-UHFFFAOYSA-N carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 18
- 229910052799 carbon Inorganic materials 0.000 description 18
- 239000004215 Carbon black (E152) Substances 0.000 description 16
- CURLTUGMZLYLDI-UHFFFAOYSA-N carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 16
- 239000007789 gas Substances 0.000 description 16
- 150000002430 hydrocarbons Chemical class 0.000 description 16
- 239000001301 oxygen Substances 0.000 description 14
- 229910052760 oxygen Inorganic materials 0.000 description 14
- MYMOFIZGZYHOMD-UHFFFAOYSA-N oxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 14
- 239000000203 mixture Substances 0.000 description 10
- 239000001257 hydrogen Substances 0.000 description 8
- 229910052739 hydrogen Inorganic materials 0.000 description 8
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 8
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- 239000003345 natural gas Substances 0.000 description 6
- 125000001183 hydrocarbyl group Chemical group 0.000 description 4
- 150000002431 hydrogen Chemical class 0.000 description 4
- 229910052742 iron Inorganic materials 0.000 description 4
- PWHULOQIROXLJO-UHFFFAOYSA-N manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 4
- 229910052748 manganese Inorganic materials 0.000 description 4
- 239000011572 manganese Substances 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 150000002739 metals Chemical class 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 229910052802 copper Inorganic materials 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 238000010494 dissociation reaction Methods 0.000 description 2
- 230000005593 dissociations Effects 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 229910052595 hematite Inorganic materials 0.000 description 2
- 239000011019 hematite Substances 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 239000003638 reducing agent Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21B—MANUFACTURE OF IRON OR STEEL
- C21B13/00—Making spongy iron or liquid steel, by direct processes
- C21B13/0073—Selection or treatment of the reducing gases
Definitions
- LOUIS G LAUREAU, OF PHILADELPHIA, PENNSYLVANIA.
- I combine with the hydrocarbon an amount of oxygen suflicient to transform the carbon of the gas into carbonic oxide. ,1 heat the hydrocarbon to the temperature of dissociation of carbon, the carbon then uniting with the oxygen, the result being carbonic oxide and hydrogen, both reducing agents. I heat these resulting gases to the proper temperature for reduction and inject them thus heated to the metallic oxides to be treated. I thereby reduce the oxides to the state of metallic sponge, which may be bloomed or melted and run into ingots.
- Figure 1 is a central vertical section 5 Fig. 2, avertical section on line X X, and Fig. 3 a horizontal section on line
- A represents the main reductionstack
- B ducts leading thereinto
- C
- the decomposition of the hydrocarbon does not absorb so much heat as the combination of carbon and oxygen into carbonic oxide generates, there is a necessary surplus of heat, which is communicated to the heating-coils. Therefore, after the operation is once started, but little heat need be communicated by means of the hearths.
- the hearths may be fired, or they may be fed with the resulting gases of reduction, and any system for supplying heat to the mixed gases may be substituted for the one shown in the exemplification.
- the carbonic oxide having been formed and having attained the temperature at which reduction is active, it, together with the hydrogen, passes to the 'stack and communicates its sensible heat to the ore.
- the body of ore does not at once reach the temperature of reduction, which is between 550 and 1,000 centigrade; but an equilibrium is gradually reached, after which the operation goes on uninterruptedly.
- the extraction of the reduced ore takes place at regular intervals at the base of the stack.
- Iron ore for instance, if in the shape of a light hematite, is well reduced at a temperature of 000 centigrade, while the hard magnetites require up to 7 50 centigrade.
- Manganese ores require up to 900 cen tigrade.
- I claim asmy invention The improvement in processes for reducing metallic oxides to the metallic state, which consists in mixing hydrocarbon gas with atmospheric air in such proportion that the oxygen of the air will transform the carbon of the hydrocarbon into carbonic oxide, subjecting the mixture to the temperature of combination of oxygen and carbon and such higher temperature as the ore reduction calls for, and injecting the carbonic oxide, hydrogen, and nitrogen thus formed into the mass of ore to be treated.
Description
(No Model.)
L. G. LAUREAU.
PROCESS OF REDUCING METALLIC OXIDES TO THE, METALLIOSTATE.
N0. 420,945. I r Patented Feb. 11 1890.
.J' f' '1 Y E3 g, mw am W: k W S UNITED STATES PATENT OFFICE;
LOUIS G. LAUREAU, OF PHILADELPHIA, PENNSYLVANIA.
PROCESS OF REDUCING METALLIC OXIDEQ TO THE METALLIC STATE.
SPECIFICATION forming part of Letters Patent No. 420,945, dated February 11, 1890- Application filed March 8, 1889. $erial No. 302,442, (No model.
To all whom it may concern.-
Be it known that I, LOUIS G. LAUREAU, of Philadelphia, and State of Pennsylvania, have invented certain new and useful Improvements in Processes of Reducing Metallic Oxides to the Metallic State, of which the following is a specification.
In the execution of my improved process I employ natural gas or equivalent hyd rocarbons.
Heretofore, so far as I know, in attempts at reduction of ores by means of natural gas the result has been defeated by the deposits of solid carbon from the gas.-
TVhile the employment of natural gas is my main contemplation, it is also in contemplation to employ the waste hydrocarbons resulting from the distillation of petroleum.
In the execution of my process I combine with the hydrocarbon an amount of oxygen suflicient to transform the carbon of the gas into carbonic oxide. ,1 heat the hydrocarbon to the temperature of dissociation of carbon, the carbon then uniting with the oxygen, the result being carbonic oxide and hydrogen, both reducing agents. I heat these resulting gases to the proper temperature for reduction and inject them thus heated to the metallic oxides to be treated. I thereby reduce the oxides to the state of metallic sponge, which may be bloomed or melted and run into ingots.
In the accompanying drawings I show an apparatus merely exemplifying in its character adapted for the execution of my improved process.
In the drawings, Figure 1 is a central vertical section 5 Fig. 2, avertical section on line X X, and Fig. 3 a horizontal section on line In the drawings, A represents the main reductionstack; B, ducts leading thereinto; C,
enlarged intermediate portions of these ducts,
Q drocarbon under pressure and leading to the I tuyeres; J, a regulating-cock in the hydrocarbon-pipe; K, a pipe to be connected with a source of air-supply under pressure, and, connecting, in common with the hydrocarbonpipe, with the tuyeres; L, a regulating-cock in the air-supply pipe; M, the base of the reduction-stack arranged in' a'common manner for the withdrawal of the reduced ore.
Having determined from the composition of the hydrocarbon the amount of oxygen required to transform its carbon to carbonic oxide, I adjust the supply of air and hydrocarbon to the tuyeres accordingly. I then fill the stack with ore broken into small pieces and close the top gas-tight. I then build fires in the hearths and get the coils of pipe in the chambers to'a cherry-red heat. I-then admit the mixed gas and air through the tuyeres. The mixture passes over the heating-coils and the oxygen of the air acts at once, combining with the carbon of the hydrocarbon, forming carbonic oxide, the hydrogen remaining free. As the decomposition of the hydrocarbon does not absorb so much heat as the combination of carbon and oxygen into carbonic oxide generates, there is a necessary surplus of heat, which is communicated to the heating-coils. Therefore, after the operation is once started, but little heat need be communicated by means of the hearths. The hearths may be fired, or they may be fed with the resulting gases of reduction, and any system for supplying heat to the mixed gases may be substituted for the one shown in the exemplification. The carbonic oxide having been formed and having attained the temperature at which reduction is active, it, together with the hydrogen, passes to the 'stack and communicates its sensible heat to the ore. The body of ore does not at once reach the temperature of reduction, which is between 550 and 1,000 centigrade; but an equilibrium is gradually reached, after which the operation goes on uninterruptedly. The extraction of the reduced ore takes place at regular intervals at the base of the stack.
The nitrogen of the air, injected with the IOO perature within bounds, thus preventing the fusing of the ores and consequent stoppage of reduction.
The ores of most metals found in nature as oxides-such as copper, iron, manganese, &c.can be reduced by my process by varying the temperature of the gases between 550 and 1,000 Centigrade, according to the different metals and physical structures of the ores. Iron ore, for instance, if in the shape of a light hematite, is well reduced at a temperature of 000 centigrade, while the hard magnetites require up to 7 50 centigrade. Manganese ores require up to 900 cen tigrade.
I claim asmy invention The improvement in processes for reducing metallic oxides to the metallic state, which consists in mixing hydrocarbon gas with atmospheric air in such proportion that the oxygen of the air will transform the carbon of the hydrocarbon into carbonic oxide, subjecting the mixture to the temperature of combination of oxygen and carbon and such higher temperature as the ore reduction calls for, and injecting the carbonic oxide, hydrogen, and nitrogen thus formed into the mass of ore to be treated.
LOUIS G. LAUREAU. \Vitnesscs:
J. W. SEE, CHARLES F. ZIEGLER.
Publications (1)
Publication Number | Publication Date |
---|---|
US420945A true US420945A (en) | 1890-02-11 |
Family
ID=2489864
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US420945D Expired - Lifetime US420945A (en) | Process of reducing metallic oxides to the metallic state |
Country Status (1)
Country | Link |
---|---|
US (1) | US420945A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6478841B1 (en) | 2001-09-12 | 2002-11-12 | Techint Technologies Inc. | Integrated mini-mill for iron and steel making |
-
0
- US US420945D patent/US420945A/en not_active Expired - Lifetime
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6478841B1 (en) | 2001-09-12 | 2002-11-12 | Techint Technologies Inc. | Integrated mini-mill for iron and steel making |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US6328783B1 (en) | Producing iron from solid iron carbide | |
US420945A (en) | Process of reducing metallic oxides to the metallic state | |
US1019965A (en) | Treatment of metals. | |
US2557650A (en) | Metallurgical process | |
US325293A (en) | Process of smelting ore by means of petroleum | |
US342607A (en) | kendill | |
US1645968A (en) | Process of making sponge iron from its oxide ores | |
US453227A (en) | Kiley porter wilson | |
US3811869A (en) | Process for the reduction of iron ores | |
GB1218912A (en) | Blast furnace operation | |
US2715575A (en) | Method of treating iron ore blast furnaces | |
US1329055A (en) | Mektuei | |
US546702A (en) | Process of and apparatus for manufacture of gas | |
US1360711A (en) | Process for the manufacture of iron and steel directly from the ore and improved apparatus therefor | |
JPS63171807A (en) | Operation method for oxygen blast furnace | |
US54215A (en) | Improvement in blast-furnaces | |
US1988929A (en) | Metallurgical furnace gas and method of controlling composition | |
US415564A (en) | Process of manufacturing gas | |
US250602A (en) | thiollier and f | |
USRE68E (en) | Improvement in the construction and heating of furnaces for metallurgic operations | |
US191749A (en) | Improvement in processes for manufacturing carbureted hydrogen gas | |
US121226A (en) | Improvement in processes for the manufacture of iron | |
US87479A (en) | Improvement in the manufacture of iron and steel | |
US3583866A (en) | Refining of iron | |
US604580A (en) | Process of and apparatus for alloying iron and hydrogen |