US1592860A - Production of carbon monoxide - Google Patents
Production of carbon monoxide Download PDFInfo
- Publication number
- US1592860A US1592860A US499674A US49967421A US1592860A US 1592860 A US1592860 A US 1592860A US 499674 A US499674 A US 499674A US 49967421 A US49967421 A US 49967421A US 1592860 A US1592860 A US 1592860A
- Authority
- US
- United States
- Prior art keywords
- carbon
- tower
- carbon monoxide
- bath
- production
- 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
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- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 title description 12
- 229910002091 carbon monoxide Inorganic materials 0.000 title description 12
- 238000004519 manufacturing process Methods 0.000 title description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 18
- 229910052799 carbon Inorganic materials 0.000 description 17
- 239000007789 gas Substances 0.000 description 14
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 12
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 12
- 229910052751 metal Inorganic materials 0.000 description 10
- 239000002184 metal Substances 0.000 description 10
- 238000006243 chemical reaction Methods 0.000 description 9
- 238000010438 heat treatment Methods 0.000 description 6
- 229910052742 iron Inorganic materials 0.000 description 6
- 239000003575 carbonaceous material Substances 0.000 description 4
- 239000000446 fuel Substances 0.000 description 4
- 238000005192 partition Methods 0.000 description 3
- 239000002893 slag Substances 0.000 description 3
- 230000003197 catalytic effect Effects 0.000 description 2
- 239000003638 chemical reducing agent Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000003245 coal Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000003500 flue dust Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 229910021404 metallic carbon Inorganic materials 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B32/00—Carbon; Compounds thereof
- C01B32/40—Carbon monoxide
Definitions
- a My invention provides for the production of reducing gases. and in particular carbon monoxide. It is found that the reaction between carbon dioxide or carbonic acid and I free carbon may be readily carried out in the presence of a molten bath.
- metals which in solution are adapted for serving as mediums for converting carbonic acid and carbon into carbon monoxide, iron is found to be particularly suitable. In its molten state iron may be said to be a catalytic agent in the sense that it serves to dissolve the carbon. and in turn, to cause its combination with carbonic acid to'produce carbon monoxide.
- Any reaction by which carbonic acid is produced may be utilized to furnish this material as the first step in the process.
- FIG. 1 is a vertical section through the gas producer,.
- Fig. 2 is a horizontal section taken on the line 22 of Fig. 1.
- a hopper 1 delivers a charge of mixed ore and carbon through a suitable conveyer 2, into tower 3.
- This tower is built upon a base 4, forming a suitable chamber 5, and a metal container or trough 6.
- One wall 7 of the tower 3 forms a partition between the chamber structure and the molten bath in the trough 6.
- a suitable communicating arch 8 is formed in the wall 7.
- the chamber 5 is adapted to be heated by any convenientmeans, not shown in the drawing.
- a conduit 9 extends from the tower 3 downwardly and into an adjacent tower 10.
- the tower 10 forms the gas reducer.
- a charging device denoted generally by the numeral 11 is used to deliver coal or other carbonaceous material to the tower 10.
- An inlet pipe 12 is carried through the lower wall of the tower 10 and terminates at the surface of the molten bath in the base of the tower. 1
- a gas out-let pipe 13 leads from the upper wall of the tower 10.
- One Wall 14 of the tower 10 is extended downward to the supporting-base 4 and has a communicating arch 15.
- the trough 16 is divided by the partition 14 into a reaction chamber 17 beneath the tower 10 and a heating chamber 18 beyond the wall 14. Suitable means are employed to provide adequate heat for the molten bath in the trough 16, preferably through the heating chamber 18.
- agitating means are provided, as for example the mechanical agitators illustrated at 19 in Fig. 2. These may be mounted upon shafts 20 and operated from mechanism 21 outside of the furnace structure. Molten metal is maintained at the requisite temperature in the various troughs by suitable heating arrangements.
- a charge of mixed ore and coal or other fuel is fed into the tower 3 and rests upon the surface of the molten bath. Carbon from the fuel'is taken into solution by the molten metal of the bath while reduction takes place between the ore and the main bod of fuel. The reduced metal is taken up y the molten bath. A certain amount of slag results from the reaction and forms upon the surface of the bath as shown at 22.
- Carbonic acid and carbon monoxide are given off during the metal reduction operation and fill the chamber of the tower 3. Under the pressure attained during this step these mixed gases are forced through pipe 9 into the molten bath 17 beneath the tower 10. i
- the molten bath 16 carries a relatively high percentage of carbon in solution. This percentage is maintained by the addition of carbonaceous material through the charging device 11 or by blowing finely divided fuel through the pipe 12 by any customary pneumatic feeding means, not shown.
- the 1 gases coming from the pipe 9 are blown into lntimate contact with the molten metal of the bath. This results in the reduction of the gases to carbon monoxide with subseuent absorption of additional carbon from t e bathor from tree carbon as the same may be added to the bath.
- the highly heated carbon mass in the tower 10 is a further reducing agent for improving the quality of the gas.
- the molten baths may be connected or exist as a single body of material and that suitable means will be provided for the withdrawal of surplus metal and of slag where the same accumulates.
- carbonic acid is utilized as an initial ingredicut it being apparent that any source of the same, or any reaction whereby it is produced may serve equally well.
- the carbonic acid produced. in the manner above set out will develop such pressure that it is forced into the reaction chamber 17 and into contact with the contained carboniferous molten iron which operates as a catalytic agent.
- the carbonic acid is converted to carbon monoxide, the necessary carbon being supplied either from the carbonaceous material resent or from the carbon contained in t e bath.
- the reduced gas passes upwardly, being improved in its quality by passing through the body of highly heated carbon. The gas is then drawn off for cooling and use.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Carbon And Carbon Compounds (AREA)
Description
J. E. LEONARZ PRODUCTION OF CARBON MONOXIDE Jul 20 1926 Filed Sept. 10, 1921 ORE AND ccdb RBON NIONOX I O5 Patented July 20, 1926.
UNITED STATES.
JOHANN EMIL LEONARZ, OF TACUBAYA, MEXICO.
PRODUCTION OF CARBON MONOXIDE.
Application filed September 10, 1921. Serial No. 499,614.
A My invention provides for the production of reducing gases. and in particular carbon monoxide. It is found that the reaction between carbon dioxide or carbonic acid and I free carbon may be readily carried out in the presence of a molten bath. Among the metals which in solution are adapted for serving as mediums for converting carbonic acid and carbon into carbon monoxide, iron is found to be particularly suitable. In its molten state iron may be said to be a catalytic agent in the sense that it serves to dissolve the carbon. and in turn, to cause its combination with carbonic acid to'produce carbon monoxide.
It is further an object of my invention to utilize for this purpose the carbonic acid resulting from the direct reduction of iron or other metals from the ore. It is found that heating a mixture of metallic oxide and carbon is sufficient to sustain the continued reaction whereby the oxide is reduced and a mixture of carbonic acid and carbon monoxide produced. The necessary heat to maintain this reaction is furnished through the hpating of the molten bath, described hereina ter. I
Any reaction by which carbonic acid is produced, may be utilized to furnish this material as the first step in the process.
For purposes of illustration one form of apparatus for carrying out my invention is shown diagrammatically in the accompanying drawing, in which Fig. 1 is a vertical section through the gas producer,. and
Fig. 2 is a horizontal section taken on the line 22 of Fig. 1.
A hopper 1 delivers a charge of mixed ore and carbon through a suitable conveyer 2, into tower 3. This tower is built upon a base 4, forming a suitable chamber 5, and a metal container or trough 6. One wall 7 of the tower 3 forms a partition between the chamber structure and the molten bath in the trough 6. A suitable communicating arch 8 is formed in the wall 7. The chamber 5 is adapted to be heated by any convenientmeans, not shown in the drawing.
A conduit 9 extends from the tower 3 downwardly and into an adjacent tower 10. The tower 10 forms the gas reducer. A charging device denoted generally by the numeral 11 is used to deliver coal or other carbonaceous material to the tower 10. An inlet pipe 12 is carried through the lower wall of the tower 10 and terminates at the surface of the molten bath in the base of the tower. 1
A gas out-let pipe 13 leads from the upper wall of the tower 10.
One Wall 14 of the tower 10 is extended downward to the supporting-base 4 and has a communicating arch 15. The trough 16 is divided by the partition 14 into a reaction chamber 17 beneath the tower 10 and a heating chamber 18 beyond the wall 14. Suitable means are employed to provide adequate heat for the molten bath in the trough 16, preferably through the heating chamber 18.
In order to insure constant and uniform circulation of the molten metal between the two divisions formed by the partitions 7 and 14, agitating means are provided, as for example the mechanical agitators illustrated at 19 in Fig. 2. These may be mounted upon shafts 20 and operated from mechanism 21 outside of the furnace structure. Molten metal is maintained at the requisite temperature in the various troughs by suitable heating arrangements.
A charge of mixed ore and coal or other fuel is fed into the tower 3 and rests upon the surface of the molten bath. Carbon from the fuel'is taken into solution by the molten metal of the bath while reduction takes place between the ore and the main bod of fuel. The reduced metal is taken up y the molten bath. A certain amount of slag results from the reaction and forms upon the surface of the bath as shown at 22.
Carbonic acid and carbon monoxide are given off during the metal reduction operation and fill the chamber of the tower 3. Under the pressure attained during this step these mixed gases are forced through pipe 9 into the molten bath 17 beneath the tower 10. i
The molten bath 16 carries a relatively high percentage of carbon in solution. This percentage is maintained by the addition of carbonaceous material through the charging device 11 or by blowing finely divided fuel through the pipe 12 by any customary pneumatic feeding means, not shown. The 1 gases coming from the pipe 9 are blown into lntimate contact with the molten metal of the bath. This results in the reduction of the gases to carbon monoxide with subseuent absorption of additional carbon from t e bathor from tree carbon as the same may be added to the bath. As the gas rises it must pass through a body of highly heated carbonaceous material which is maintained in the tower 10. This serves as a washer of gas returning any flue dust that may have been carried along. Slag 23 will form on the surface of the bath. At the same time the highly heated carbon mass in the tower 10 is a further reducing agent for improving the quality of the gas. It will beapparent that the molten baths may be connected or exist as a single body of material and that suitable means will be provided for the withdrawal of surplus metal and of slag where the same accumulates.
By the procedure outlined above carbonic acid is utilized as an initial ingredicut it being apparent that any source of the same, or any reaction whereby it is produced may serve equally well. The carbonic acid produced. in the manner above set out will develop such pressure that it is forced into the reaction chamber 17 and into contact with the contained carboniferous molten iron which operates as a catalytic agent. Under the conditions of temperature existing in this chamber the carbonic acid is converted to carbon monoxide, the necessary carbon being supplied either from the carbonaceous material resent or from the carbon contained in t e bath. The reduced gas passes upwardly, being improved in its quality by passing through the body of highly heated carbon. The gas is then drawn off for cooling and use.
While I have shown and described one mode of carrying out my invention, it will be apparent that many changes may be made in minor details and steps and it is to be understood that the invention is as defined in the following claims.
What I claim is:
1. The production of carbon monoxide by heating an oxide of iron with carbon without access of air, passing the resultant gas through a molten bath and adding carbon to said bath.
2. The production of carbon monoxide by heating an oxide of iron With carbon without access of air, passing the resultant gas through a molten bath by the pressure developed by the reaction of the oxide and the carbon, and maintaining carbon in the molten bath.
In testimony whereof, I have hereunto affixed my signature.
J OHANN EMIL LEONARZ.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US499674A US1592860A (en) | 1921-09-10 | 1921-09-10 | Production of carbon monoxide |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US499674A US1592860A (en) | 1921-09-10 | 1921-09-10 | Production of carbon monoxide |
Publications (1)
Publication Number | Publication Date |
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US1592860A true US1592860A (en) | 1926-07-20 |
Family
ID=23986227
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US499674A Expired - Lifetime US1592860A (en) | 1921-09-10 | 1921-09-10 | Production of carbon monoxide |
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US (1) | US1592860A (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2953445A (en) * | 1955-08-11 | 1960-09-20 | Rummel Roman | Gasification of fuels and decomposition of gases |
US3385668A (en) * | 1966-11-22 | 1968-05-28 | Horizons Inc | Preparation of carbon monoxide by reaction of carbon dioxide with finely divided carbon in a fused salt bath containing a dissolved catalyst |
US3505018A (en) * | 1966-10-31 | 1970-04-07 | Texas Instruments Inc | Reforming hydrocarbon fuels |
US3526478A (en) * | 1968-11-01 | 1970-09-01 | Black Sivalls & Bryson Inc | Generation of hydrogen from sulfurbearing carbonaceous fuel |
US3533739A (en) * | 1968-04-01 | 1970-10-13 | Black Sivalls & Bryson Inc | Combustion of sulfur-bearing carbonaceous fuel |
US3647379A (en) * | 1968-08-22 | 1972-03-07 | Rheinische Braunkohlewerke Ag | Method of gasifying water-containing coal |
US4181504A (en) * | 1975-12-30 | 1980-01-01 | Technology Application Services Corp. | Method for the gasification of carbonaceous matter by plasma arc pyrolysis |
-
1921
- 1921-09-10 US US499674A patent/US1592860A/en not_active Expired - Lifetime
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2953445A (en) * | 1955-08-11 | 1960-09-20 | Rummel Roman | Gasification of fuels and decomposition of gases |
US3505018A (en) * | 1966-10-31 | 1970-04-07 | Texas Instruments Inc | Reforming hydrocarbon fuels |
US3385668A (en) * | 1966-11-22 | 1968-05-28 | Horizons Inc | Preparation of carbon monoxide by reaction of carbon dioxide with finely divided carbon in a fused salt bath containing a dissolved catalyst |
US3533739A (en) * | 1968-04-01 | 1970-10-13 | Black Sivalls & Bryson Inc | Combustion of sulfur-bearing carbonaceous fuel |
US3647379A (en) * | 1968-08-22 | 1972-03-07 | Rheinische Braunkohlewerke Ag | Method of gasifying water-containing coal |
US3526478A (en) * | 1968-11-01 | 1970-09-01 | Black Sivalls & Bryson Inc | Generation of hydrogen from sulfurbearing carbonaceous fuel |
US4181504A (en) * | 1975-12-30 | 1980-01-01 | Technology Application Services Corp. | Method for the gasification of carbonaceous matter by plasma arc pyrolysis |
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