US2691573A - Desulfurization in the gasification of coal - Google Patents
Desulfurization in the gasification of coal Download PDFInfo
- Publication number
- US2691573A US2691573A US200984A US20098450A US2691573A US 2691573 A US2691573 A US 2691573A US 200984 A US200984 A US 200984A US 20098450 A US20098450 A US 20098450A US 2691573 A US2691573 A US 2691573A
- Authority
- US
- United States
- Prior art keywords
- gasification
- carbonyl
- metal
- coal
- iron
- 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
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
- C10J3/00—Production of combustible gases containing carbon monoxide from solid carbonaceous fuels
- C10J3/46—Gasification of granular or pulverulent flues in suspension
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L9/00—Treating solid fuels to improve their combustion
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
- C10J2300/00—Details of gasification processes
- C10J2300/09—Details of the feed, e.g. feeding of spent catalyst, inert gas or halogens
- C10J2300/0913—Carbonaceous raw material
- C10J2300/093—Coal
- C10J2300/0933—Coal fines for producing water gas
Definitions
- This invention relates toan' improvedprocess for the removal of sulfur simultaneously with the gasification of carbonaceous e materials
- Sulfur compounds may be re moved from the gasbyi many methods" including physical absorptionand chemical reaction" but because of the volume" of the gas *streamand-the presence of high carbon dioxide: content; these methods are expensive.
- the present invention provides a" method "for the removal of sulfur simultaneously with” the gasifikiation of a carbonaceous material thus eliminating costly' purification steps:
- iron-onanoth'er metal carbonyl formed'from finely divided-iron and a portion of the carbon monoxide containing gas from the'gasification step; is condensed anda'b sorbed' on the surface ofthe coal particles;
- the carbonyl treated coal particles are then'- fed to a gasification-chamber: At the temperature of gasificationthe carbonyl is" decomposed"to'- ele'e mental iron which is finely dispersed through outtheproducts of initial gasificationandis free to react with sulfur compounds. Iromsulfid'e-is formed and is takenofi with the ash, and agasification'productwith alowered'sulfur content is produced.
- Thepowdered coal. being at 'roonr temperature; the iron: carbonyl: is: both condensed and. absorbed ion the surfacestof the coal particles in chamber H:
- the powdered coal .is withdrawn from chamberrlrl througl'i-iilines. l t ite a separation zone: l5.
- Gasesfare removed fromizthefseparation zone *l'stthroughiline-F [6.
- the powd'eredzcoal is withdrawn from the separation zone l5 through line I! and blown into the gasification chamber I8 together with oxygen from line I! and/or steam from line 25.
- the carbonyl Upon entering the gasification chamber [8, the carbonyl is decomposed to elemental iron which is finely dispersed throughout the product of initial combustion and is free to react with sulfur compounds.
- Typical operating conditions for the first gasification stage are:
- the lower temperature in the second stage gasification may be obtained by a water or steam quench 29, or by any cooling method known to the art.
- a lower temperature results in an even lower hydrogen sulfide concentration and would be desirable for fuel gas since methanation, which is the formation of methane, would occur and be catalyzed by the iron.
- the high temperature is desirable to reduce the residual hydrocarbon, though sulfur removal is less complete and a further sulfur removal step may be desirable.
- the gasification products are withdrawn through line 20 to a separation zone 2! Where the ash and iron sulfide are taken off through line 22.
- the gasification products are withdrawn through line 23 and passed to cooling and purification zones 26. Any cooling method and any scrubbing oil known to the art may be used. Tar oil and sludge are removed through line 2'! and water removed through line 24.
- the fuel gas is removed through line 28. A part of the fuel gas containing carbon monoxide is recycled through line 3
- coal has as its full equivalent other gasifiable carbonaceous materials, the essence of the present invention being substantially as set forth in the following paragraph.
- a process for the gasification of a solid powdered carbonaceous material containing sulfur which comprises introducing said material and a metal carbonyl into a gasification zone, subjecting said mixture to gasification conditions with the introduction of an oxygen-supplying gas so as to supply the heat of reaction and react the metal of the metal carbonyl with the sulfur component of the carbonaceous material to produce the metal sulfide, removing the metal sulfide from the gases produced and recovering said gases.
- a process according to claim 1 wherein the solid carbonaceous material is coal and the carbonyl is iron carbonyl.
- a process for the gasification of a solid carbonaceous material containing sulfur which comprises subdividing said material to form a powder thereof; admixing with said powder a metal carbonyl; then introducing said powder admixed with said metal carbonyl into a gasification zone, gasifying said powder at a gasification temperature; then separating gases thus produced from solid residue of the carbonaceous material and metal sulfide formed and recovering said gases.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Combustion & Propulsion (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Industrial Gases (AREA)
Description
Patented Oct. 12, 1954 DESULEURIZATIDN IN THE GASIFICATION OF COA'IJ Bertrand Ji -M'ayland;- Bartlesvillq: 0kla.,. assignorr to Phillipstlietroleum Company, a corporation ofiDelaware:
'tClaims:v 1
This invention relates toan' improvedprocess for the removal of sulfur simultaneously with the gasification of carbonaceous e materials;
The sulfur content of 'coals 'maybe as-high as 10 per cent by weight or more andfdrthismeason fuel gas or synthesis gas' made-by conventional coahgasifibation 'processesis; in many cases; high in sulfur, which isundesirable for various-reasons such ascorrosion; catalyst poisoning; gum formation, etc. Sulfur compounds may be re moved from the gasbyi many methods" including physical absorptionand chemical reaction" but because of the volume" of the gas *streamand-the presence of high carbon dioxide: content; these methods are expensive.
The present" invention provides a" method "for the removal of sulfur simultaneously with" the gasifikiation of a carbonaceous material thus eliminating costly' purification steps: According tothe present invention; iron-onanoth'er metal carbonyl, formed'from finely divided-iron and a portion of the carbon monoxide containing gas from the'gasification step; is condensed anda'b sorbed' on the surface ofthe coal particles; The carbonyl treated coal particles" are then'- fed to a gasification-chamber: At the temperature of gasificationthe carbonyl is" decomposed"to'- ele'e mental iron which is finely dispersed through outtheproducts of initial gasificationandis free to react with sulfur compounds. Iromsulfid'e-is formed and is takenofi with the ash, and agasification'productwith alowered'sulfur content is produced.
In.-.order to have the ironiwidely dispersed-isothat excessive amounts will notice requiredzithe following'procedure is preferred. Finelyydivided iron-fromany source such as forexampleva; used fluidized iron synthesis catalyst, is contacted with carbon monoxide containing gas from the gasification step at the most favorable conditions of temperature and pressure for carbonyl formation and volatilization. These conditions are given in the published literature. See, for example, Researches on the Metallic C'arbonyls, R. L. Mond and A. E. Wallis, Journal Chem. Soc., 121, 29-32 (1922). According to this reference, favorable conditions ofiron carbonyl formations are:
2-. inc-possession of this.disclosureathat:metalsxother thanzironzmay: beus'ectl in vth-isr processv Theegas containing: the; hunt-carbonyl; vaportis :zthen"; con; tactedirwithtpowdered coaliin thecoalafeedtchamr-v ber of a: gasification plants. Withisomencoo-ling the-"irorrtcarbonyl isaboth condnsedrand: absorbed on:ther-:.surface.:offthe coal particles: Uponaene tering .the gasificationr chambert'the: carbonyl. is decomposeditotelemental ironiwhich'is :then free torreact withcsulfurrcompoundsr In therdrawing thererisdiagrammatically rep resented-r. one form. of: apparatuswhich .may'i' be used." tot-practice? that process: of my invention; Thetprocessrsis'edescrihedvwitli respect:to coaltbut ittcamhereadily modifiedtior any-carbonaceous material i-suchi as::- ground? oil shale; shale: oi'L. res finery-rresiduum; etc. Inzpreparing the coal or other: carbonaceous materiallfor gasification;..it isa-desirable2 to: pnlverize .it toarelativelyfiherstate of.:.subd-ivision-,". preferably suchi that: it WilliDEiSS I the: coal: is: conducted; through: feed? line 10K to chamber H. In chamheri'll;.the'rpowderedrcoai is zcontact'edzwith :ironucarbonyl vapor containing gassfrom line::l2. z This =.gas issa 'recyclegas from the-s gasifi-cation; process, containswcarbon: mon= oxid'e andfis contacted-.twith-faifinely Jdividedsiiron in chamber l3.atsuitable conditions tot form'iiiron' carbonyli. Thepowdered coal. being at 'roonr temperature; the iron: carbonyl: is: both condensed and. absorbed ion the surfacestof the coal particles in chamber H: The powdered: coal .is withdrawn from chamberrlrl througl'i-iilines. l t ite a separation zone: l5. Gasesfare removed: fromizthefseparation zone *l'stthroughiline-F [6. The powd'eredzcoal is withdrawn from the separation zone l5 through line I! and blown into the gasification chamber I8 together with oxygen from line I!) and/or steam from line 25. Upon entering the gasification chamber [8, the carbonyl is decomposed to elemental iron which is finely dispersed throughout the product of initial combustion and is free to react with sulfur compounds. Typical operating conditions for the first gasification stage are:
Preferred Broad Range Range Temperature, F 1,400 to 3,000.... 1,800 to 2,500. Pressure, Atms 1.5 to 30 2 to 15. Contact time, Seconds 0.1 to 10 l to 5 It will be apparent to one skilled in the art A lower temperature will give a lower hydrogen sulfide concentration and would be desirable for fuel gas since methanation would occur and be catalyzed by the iron. Typical operating conditions for the second gasification stage are:
The lower temperature in the second stage gasification may be obtained by a water or steam quench 29, or by any cooling method known to the art.
The thermodynamic equilibrium for the system Fe-FeS--H2H2S is such that at 1600" F., H2S/I-I2=300 With a concentration of hydrogen at 40 per cent, hydrogen sulfide is 0.13 per cent; thus most of the sulfur leaves as iron sulfide in the ash from the coal. A lower temperature results in an even lower hydrogen sulfide concentration and would be desirable for fuel gas since methanation, which is the formation of methane, would occur and be catalyzed by the iron. For synthesis gas the high temperature is desirable to reduce the residual hydrocarbon, though sulfur removal is less complete and a further sulfur removal step may be desirable.
The gasification products are withdrawn through line 20 to a separation zone 2! Where the ash and iron sulfide are taken off through line 22. The gasification products are withdrawn through line 23 and passed to cooling and purification zones 26. Any cooling method and any scrubbing oil known to the art may be used. Tar oil and sludge are removed through line 2'! and water removed through line 24. The fuel gas is removed through line 28. A part of the fuel gas containing carbon monoxide is recycled through line 3| to the iron chamber 13, where iron carbonyl is formed from contacting iron with the carbon monoxide containing gas. This gas and iron carbonyl contained therein are then withdrawn through line l2 to contact the coal in zone H as previously described.
Herein and in the claims it is to be understood that coal has as its full equivalent other gasifiable carbonaceous materials, the essence of the present invention being substantially as set forth in the following paragraph.
Reasonable variation and some modification are possible within the scope of the foregoing disclosure, drawing, and the appended claims to the invention, the essence of which is that in situ formation of an elemental metal, e. g. iron, from a metal carbonyl, is used in a gasification process to simultaneously desulfurize the gases being pro- 4 duced and that a method for so doing has been set forth.
I claim:
1. A process for the gasification of a solid powdered carbonaceous material containing sulfur which comprises introducing said material and a metal carbonyl into a gasification zone, subjecting said mixture to gasification conditions with the introduction of an oxygen-supplying gas so as to supply the heat of reaction and react the metal of the metal carbonyl with the sulfur component of the carbonaceous material to produce the metal sulfide, removing the metal sulfide from the gases produced and recovering said gases.
2. A process according to claim 1 in which the gasification is carried out in two gasification stages and in which there is effected a cooling of the gases intermediate said stages so as to reduce the temperature of the gases entering into said second stage to a level at which methanation is effected.
3. A process according to claim 1 wherein the solid carbonaceous material is coal and the carbonyl is iron carbonyl.
4. A process according to claim 1 wherein the gasification is effected at a temperature in the range 1400-3000 F. under a pressure of 1.5-30 atmospheres and the time is of the order of 0.1-10 seconds.
5. A process for the gasification of a solid carbonaceous material containing sulfur, which comprises subdividing said material to form a powder thereof; admixing with said powder a metal carbonyl; then introducing said powder admixed with said metal carbonyl into a gasification zone, gasifying said powder at a gasification temperature; then separating gases thus produced from solid residue of the carbonaceous material and metal sulfide formed and recovering said gases.
6. A process according to claim 5 wherein a portion of the gases formed are contacted with a metal to form additional metal carbonyl.
7. A process according to claim 5 in which the gasification is carried out in two gasification stages and in which there is effected a cooling of the gases intermediate said stages so as to reduce the temperature of the gases entering into said second stage to a level at which methanation is efiected.
References Cited in the file of this patent UNITED STATES PATENTS Number Name Date 676,245 Strache June 11, 1901 809,087 Blackmore Jan. 2, 1906 2,221,061 Simpson Nov. 12, 1940
Claims (1)
1. A PROCESS FOR THE GASIFICATION OF A SOLID POWDERED CARBONACEOUS MATERIAL CONTAINING SULFUR WHICH COMPRISES INTRODUCING SAID MATERIAL AND A METAL CARBONYL INTO A GASIFICATION ZONE, SUBJECTING SAID MIXTURE TO GASIFICATION CONDITIONS WITH THE INTRODUCTION OF AN OXYGEN-SUPPLYING GAS SO AS TO SUPPLY THE HEAT OF REACTION AND REACT THE METAL OF THE METAL CARBONYL WITH THE SULFUR COMPONENT OF THE CARBONACEOUS MATERIAL TO PRODUCE THE METAL SULFIDE, REMOVING THE METAL SULFIDE FROM THE GASES PRODUCED AND RECOVERING SAID GASES.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US200984A US2691573A (en) | 1950-12-15 | 1950-12-15 | Desulfurization in the gasification of coal |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US200984A US2691573A (en) | 1950-12-15 | 1950-12-15 | Desulfurization in the gasification of coal |
Publications (1)
Publication Number | Publication Date |
---|---|
US2691573A true US2691573A (en) | 1954-10-12 |
Family
ID=22743995
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US200984A Expired - Lifetime US2691573A (en) | 1950-12-15 | 1950-12-15 | Desulfurization in the gasification of coal |
Country Status (1)
Country | Link |
---|---|
US (1) | US2691573A (en) |
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2867516A (en) * | 1954-08-18 | 1959-01-06 | Du Pont | Process for burning gaseous fuels |
US3506590A (en) * | 1967-03-11 | 1970-04-14 | Huettenwerk Oberhausen Ag | Manufacture of synthesis-,hydrogenating-,or reduction-gas |
US3533739A (en) * | 1968-04-01 | 1970-10-13 | Black Sivalls & Bryson Inc | Combustion of sulfur-bearing carbonaceous fuel |
USB375220I5 (en) * | 1973-06-29 | 1975-01-28 | ||
US4070160A (en) * | 1977-05-09 | 1978-01-24 | Phillips Petroleum Company | Gasification process with zinc condensation on the carbon source |
US4095960A (en) * | 1976-11-09 | 1978-06-20 | Schuhmann Reinhardt Jun | Apparatus and method for the gasification of solid carbonaceous material |
FR2473350A1 (en) * | 1977-07-21 | 1981-07-17 | Trw Inc | |
US4710483A (en) * | 1977-07-21 | 1987-12-01 | Trw Inc. | Novel carbonaceous material and process for producing a high BTU gas from this material |
EP0305047A2 (en) * | 1987-08-28 | 1989-03-01 | Texaco Development Corporation | High temperature desulfurization of synthesis gas |
WO1994025544A1 (en) * | 1993-04-30 | 1994-11-10 | Shell Oil Company | Method of reducing hcn in synthesis gas |
US5720785A (en) * | 1993-04-30 | 1998-02-24 | Shell Oil Company | Method of reducing hydrogen cyanide and ammonia in synthesis gas |
US5895508A (en) * | 1996-08-09 | 1999-04-20 | The United States Of America As Represented By The United States Department Of Energy | Down-flow moving-bed gasifier with catalyst recycle |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US676245A (en) * | 1896-02-19 | 1901-06-11 | Int Du Gaz D Eau Brevets Strache Sa Soc | Apparatus for making water-gas. |
US809087A (en) * | 1904-12-12 | 1906-01-02 | Black Ford Utility Oil Company | Process of eliminating sulfur from the sulfur-containing constituents of petroleum. |
US2221061A (en) * | 1939-02-07 | 1940-11-12 | Kenneth M Simpson | Process of making iron and nickel alloys |
-
1950
- 1950-12-15 US US200984A patent/US2691573A/en not_active Expired - Lifetime
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US676245A (en) * | 1896-02-19 | 1901-06-11 | Int Du Gaz D Eau Brevets Strache Sa Soc | Apparatus for making water-gas. |
US809087A (en) * | 1904-12-12 | 1906-01-02 | Black Ford Utility Oil Company | Process of eliminating sulfur from the sulfur-containing constituents of petroleum. |
US2221061A (en) * | 1939-02-07 | 1940-11-12 | Kenneth M Simpson | Process of making iron and nickel alloys |
Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2867516A (en) * | 1954-08-18 | 1959-01-06 | Du Pont | Process for burning gaseous fuels |
US3506590A (en) * | 1967-03-11 | 1970-04-14 | Huettenwerk Oberhausen Ag | Manufacture of synthesis-,hydrogenating-,or reduction-gas |
US3533739A (en) * | 1968-04-01 | 1970-10-13 | Black Sivalls & Bryson Inc | Combustion of sulfur-bearing carbonaceous fuel |
USB375220I5 (en) * | 1973-06-29 | 1975-01-28 | ||
US3920417A (en) * | 1973-06-29 | 1975-11-18 | Combustion Eng | Method of gasifying carbonaceous material |
US4095960A (en) * | 1976-11-09 | 1978-06-20 | Schuhmann Reinhardt Jun | Apparatus and method for the gasification of solid carbonaceous material |
US4070160A (en) * | 1977-05-09 | 1978-01-24 | Phillips Petroleum Company | Gasification process with zinc condensation on the carbon source |
FR2473350A1 (en) * | 1977-07-21 | 1981-07-17 | Trw Inc | |
US4710483A (en) * | 1977-07-21 | 1987-12-01 | Trw Inc. | Novel carbonaceous material and process for producing a high BTU gas from this material |
EP0305047A2 (en) * | 1987-08-28 | 1989-03-01 | Texaco Development Corporation | High temperature desulfurization of synthesis gas |
EP0305047A3 (en) * | 1987-08-28 | 1989-04-12 | Texaco Development Corporation | High temperature desulfurization of synthesis gas |
JPH01131298A (en) * | 1987-08-28 | 1989-05-24 | Texaco Dev Corp | Production of synthetic gas |
WO1994025544A1 (en) * | 1993-04-30 | 1994-11-10 | Shell Oil Company | Method of reducing hcn in synthesis gas |
US5720785A (en) * | 1993-04-30 | 1998-02-24 | Shell Oil Company | Method of reducing hydrogen cyanide and ammonia in synthesis gas |
US5895508A (en) * | 1996-08-09 | 1999-04-20 | The United States Of America As Represented By The United States Department Of Energy | Down-flow moving-bed gasifier with catalyst recycle |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US2691573A (en) | Desulfurization in the gasification of coal | |
US3812017A (en) | Desulfurized char with phosphoric acid | |
KR850001717A (en) | Process for producing acetylene and synthesis or reducing gas from coal by arc method | |
US2963348A (en) | Hydrocarbon conversion process | |
JPS6274993A (en) | Production of gas containing carbon monoxide and hydrogen | |
EP0378892B1 (en) | Partial oxidation of sulfurcontaining solid carbonaceous fuel | |
US4082146A (en) | Low temperature oxidation of hydrogen sulfide in the presence of oil shale | |
US4047898A (en) | Upgrading of solid fuels | |
CA1036358A (en) | Process for the gasification of coal | |
US4954137A (en) | Inhibition of sulfide inclusion in slag | |
US3600130A (en) | Desulfurization of fluid petroleum coke | |
JPS63159496A (en) | Method and apparatus for treating raw gas | |
GB1496410A (en) | Process for producing a gaseous product from carbonaceous material | |
US4270928A (en) | Desulfurization of carbonaceous materials | |
JPS6362524A (en) | Treatment of gas containing sulfur and hydrocarbon | |
US4755372A (en) | Catalytic sulfur degassing | |
US1799359A (en) | Water-gas process | |
US4748141A (en) | Metal sulfide catalyst preparation | |
US4359451A (en) | Desulfurization of carbonaceous materials | |
US4786291A (en) | Method for increasing steam decomposition in a coal gasification process | |
US4888029A (en) | Desulfurization of carbonaceous materials | |
GB2025453A (en) | Recovery of ungasified solid fuel particles from suspension in water | |
JPS6274994A (en) | Gas purifying method | |
US4475925A (en) | Gasification process for carbonaceous materials | |
US4121663A (en) | Removing hydrogen sulfide from a gas |