GB2180849A - Producing clean gas containing hydrogen and carbon monoxide - Google Patents

Producing clean gas containing hydrogen and carbon monoxide Download PDF

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Publication number
GB2180849A
GB2180849A GB08622866A GB8622866A GB2180849A GB 2180849 A GB2180849 A GB 2180849A GB 08622866 A GB08622866 A GB 08622866A GB 8622866 A GB8622866 A GB 8622866A GB 2180849 A GB2180849 A GB 2180849A
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United Kingdom
Prior art keywords
gas
reaction chamber
hydrocarbon
carbon monoxide
containing carbon
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.)
Granted
Application number
GB08622866A
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GB2180849B (en
GB8622866D0 (en
Inventor
Sven Santen
Lars Bentell
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SKF Steel Engineering AB
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SKF Steel Engineering AB
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by SKF Steel Engineering AB filed Critical SKF Steel Engineering AB
Publication of GB8622866D0 publication Critical patent/GB8622866D0/en
Publication of GB2180849A publication Critical patent/GB2180849A/en
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Publication of GB2180849B publication Critical patent/GB2180849B/en
Expired legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B3/00Hydrogen; Gaseous mixtures containing hydrogen; Separation of hydrogen from mixtures containing it; Purification of hydrogen
    • C01B3/02Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen
    • C01B3/32Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B3/00Hydrogen; Gaseous mixtures containing hydrogen; Separation of hydrogen from mixtures containing it; Purification of hydrogen
    • C01B3/50Separation of hydrogen or hydrogen containing gases from gaseous mixtures, e.g. purification
    • C01B3/56Separation of hydrogen or hydrogen containing gases from gaseous mixtures, e.g. purification by contacting with solids; Regeneration of used solids
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10KPURIFYING OR MODIFYING THE CHEMICAL COMPOSITION OF COMBUSTIBLE GASES CONTAINING CARBON MONOXIDE
    • C10K1/00Purifying combustible gases containing carbon monoxide
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10KPURIFYING OR MODIFYING THE CHEMICAL COMPOSITION OF COMBUSTIBLE GASES CONTAINING CARBON MONOXIDE
    • C10K1/00Purifying combustible gases containing carbon monoxide
    • C10K1/20Purifying combustible gases containing carbon monoxide by treating with solids; Regenerating spent purifying masses

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Combustion & Propulsion (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • General Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Carbon And Carbon Compounds (AREA)
  • Industrial Gases (AREA)
  • Hydrogen, Water And Hydrids (AREA)

Abstract

In a method of producing a gas containing carbon monoxide and hydrogen, in which method the gas does not need to be subjected to energy-consuming and costly scrubbing steps before being used as reduction gas, combustion gas or synthesis gas, the gas is produced from material containing carbon and/or hydrocarbon and oxidant and is supplied to a reaction chamber (2) simultaneously with a gas heated by plasma generator (at 3), in order to crack the hydrocarbon in the gas. The gas may be passed through a limestone or dolomite filling to the remove sulphur therefrom. <IMAGE>

Description

SPECIFICATION A method of producing a clean gas containing carbon monoxide and hydrogen The present invention relates to a method of producing a gas containing carbon monoxide and hydrogen, permitting the use of commercially known technology and utilizing any form of starting material containing carbon and/or hydrocarbon, according to which the gas does not need to be subjected to energy-consuming and costly scrubbing steps before being used as reduction gas, combustion gas or synthesis gas.
In processes utilizing combustion to supply energy, and in processes utilizing starting materials other than dried coke, such as bituminous coal, peat and the like, a gas is obtained which contains H20 and hydrocarbon as well as CO+H2.
Normally a maximum CO2+H2O content of about 10% in the gas is aimed at, while at the same time the content of heavy hydrocarbons should be as close to 0% as possible.
In traditional gasification processes using oxygen gas (air) and steam, where gas and carbonaceous material move in counter-flow, it is possible to make extremely good use of the heat but, due to the low reaction temperature, this gas will contain large amounts of tar. Furthermore, a residual product is obtained in the form of ash, which is difficult to dispose of in a manner not detrimental to the environment. Considerable advantages can be gained by increasing the reaction temperature in the combustion stage so that the ash melts, and by increasing the process pressure. The solidified slag drawn off is extremely resistant to leaching and the production per unit volume of the reactor is increased.Furthermore, the excess oxygen can be kept at a reasonable level for reduction processes, i.e. less of the carbon monoxide formed need be combusted to CO2 to cover thermal losses, for instance. However, the problem of tar still remains, and the gas therefore cannot be used directly as the reduction gas, for instance.
The principal object of the present invention is thus to achieve a method which will permit the use of any form of starting material containing carbon and/or hydrocarbon for the gas generation, while also utilizing commercially known technology, in which the gas does not need to be subjected to energy-consuming and costly scrubbing steps before being used as reduction gas, combustion gas or synthesis gas.
The principal object is achieved by the method according to the present invention in which the gas produced from material containing carbon and/or hydrocarbon and oxidant is supplied to a supplementary reaction chamber simultaneously with a gas heated by plasma generator, in order to crack the hydrocarbon in the gas.
It has been found that by supplying a hot gas, heated by plasma generator and thus having extremely high energy density, a thermal disintegration of the hydrcarbon in the gas from the gasifier is obtained, as well as the reaction with H2O, 02 and/or CO2 in the gas to form H2 and CO. Due to the high energy density in the gas supplied, a comparatively small volume of gas is required, which thus makes the process possible.
The gas can be produced by means of pyrolysis or partial combustion of material containing carbon and/or hydrocarbon, such as peat, pit coal, anthracite, or forest waste. If coke-oven gas derived from pyrolysis of pit coal is to be used there will be other contaminants as well as hydrocarbons. A great advantage with the invention is that these will also be cracked in the supplementary reaction chamber.
According to one embodiment of the invention, after passing the supplementary reaction chamber, the gas is conducted through a limestone or dolomite filling to remove sulphur. The limestone or dolomite used for said sulphur purification will also act as catalyst in cracking hydrocarbon and in the reaction with oxidant. This enables the electrical energy consumption to be correspondingly lowered in the supplementary reaction chamber.
According to another embodiment of the invention the content of CO2+H20 in the gas from the supplementary reaction chamber is controlled to below 5%.
Additional advantages and features of the invention will be revealed in the following detailed description with reference to the accompanying drawing showing schematically the flowchart for a gas-producing process according to the present invention connected to a subsequent reduction process.
A crude gas is produced in a gasifier or coke oven designated 1. The crude gas generated is supplied to a supplementary reaction chamber 2. At least one plasma generator 3 is arranged in conjunction with the supplementary reaction chamber, for the supply of a hot gas having high energy density. The hydrocarbon in the crude gas is cracked in the supplementary reaction chamber and reacts to form CO+H2. Finely divided coke or H20 may be introduced through lances 4 in the supplementary reaction chamber, to adjust the hydrogen/carbon ratio.
After this the gas is subjected to sulphur purification in the shaft 5 which contains a filling 6 of limestone or dolomite supplied through a gastight sluice arrangement 7 and consumed filling is withdrawn at the bottom of the shaft through a gastight sluice arrangement 8. Any hydrocarbons remaining in the gas are also catalytically cracked in the limestone or dolomite filling. This can be utilized to reduce the electric energy consumed in the plasma generator 3 used for thermal disintegration of the hydrocarbon content.
The gas purified in this way and containing substantially only H2+CO and a small quantity of H20+CO2, can then be transported to a chamber 9 to be controlled with respect to temperature and composition before entering a shaft furnace 10 for reduction of oxidic material.
The gas produced is supplied through an inlet 12 at the bottom of the shaft furnace 10 and is caused to flow in counter-flow with the material containing metal oxide. The partially consumed gas containing impurities and dust is withdrawn through an outlet 13 and cleaned in a scrubber 14.
The cleaned, partially consumed gas can then be used for other purposes, as indicated by the filter 15. If necessary, some of the gas can be recirculated in the process via pipes 16, 16a, 1 6b and may be used, for instance, in the mixing chamber 9 to control the temperature and composition of the gas to be introduced into the shaft. Part of the recirculated gas may also be used in the plasma generator in conjunction with the supplementary reaction chamber.
The invention is further illustrated by the following example.
Example 10 ton forest waste containing 30% water and the following composition C H O N S Ash 51 6,2 42 0,2 0,5 0,5% is introduced at the top of a counter-flow gasifier per hour while an oxidant is introduced at the bottom of the gasifier in the form of air heated to 1000 C. The air added is 3700 Nm3. The composition of the top gas will be CO CO2 H2 H20 N2 CH4 25,8 9,8 41,1 4,8 15,8 2,9% At the same time a tar sample is withdrawn which indicates that the gas contains 3,2 gram tar/Nm3.
The temperature of the gas leaving is 550 C and its volume is approximately 17200 Nm3. The gas is now supplied to a supplementary reaction chamber and heated using air heated in plasma generators. The quantity of air required is only about 2100 Nm3. With the aid of the plasma generator the temperature of the gas entering is increased to 1250"C, with a consumption of approximately 8,7 MWh electric energy.
The methane and tar contents are thus removed from the heated pyrolysis gas and the gas leaving the chamber will have the following composition CO CO2 H2 H20 N2 28,6 4,8 29,6 13,6 23,4 The quantity of gas leaving will be approximately 19900 Nm3.

Claims (5)

1. A method of producing a gas containing carbon monoxide and hydrogen which gas is substantially free from tar and is suitable for use as reduction gas, combustion gas or synthesis gas, comprising producing a gas from an oxidant and material containing carbon and/or hydrocarbon and supplying the gas to a reaction chamber simultaneously with gas heated by plasma generator, such that hydrocarbon in the gas is cracked.
2. A method according to claim 1, wherein after passing the supplementary reaction chamber, the gas is conducted through a-limestone or dolomite filling to remove sulphur, such that any remaining hydrocarbon is cracked and reaction with the oxidation occurs.
3. A method according to claims 1 or claim 2, wherein finely divided coke and/or water is injected into the supplementary reaction chamber.
4. A method according to any of claims 1 to 3, wherein the content of CO2+H2O in the gas from the supplementary reaction chamber is controlled to below 5%.
5. A method according to claim 1 and substantially as hereinbefore described with reference to the Example.
GB8622866A 1985-09-25 1986-09-23 A method of producing a clean gas containing carbon monoxide and hydrogen Expired GB2180849B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SE8504439A SE457355B (en) 1985-09-25 1985-09-25 MAKE SURE TO PREPARE A CLEAN, CARBON OXIDE AND GAS GAS INCLUDING GAS

Publications (3)

Publication Number Publication Date
GB8622866D0 GB8622866D0 (en) 1986-10-29
GB2180849A true GB2180849A (en) 1987-04-08
GB2180849B GB2180849B (en) 1989-12-28

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GB8622866A Expired GB2180849B (en) 1985-09-25 1986-09-23 A method of producing a clean gas containing carbon monoxide and hydrogen

Country Status (13)

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JP (1) JP2509192B2 (en)
AT (1) AT396366B (en)
AU (1) AU589997B2 (en)
BE (1) BE905480A (en)
BR (1) BR8701328A (en)
CA (1) CA1309589C (en)
DE (1) DE3631015A1 (en)
FI (1) FI863726A (en)
FR (1) FR2587717B1 (en)
GB (1) GB2180849B (en)
IL (1) IL80027A0 (en)
IT (1) IT1213497B (en)
SE (1) SE457355B (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0310584A2 (en) * 1987-10-02 1989-04-05 TPS Termiska Processer Aktiebolag Refining of raw gas
US4880439A (en) * 1988-05-05 1989-11-14 Texaco Inc. High temperature desulfurization of synthesis gas
US5213587A (en) * 1987-10-02 1993-05-25 Studsvik Ab Refining of raw gas
EP0628621A2 (en) * 1993-06-11 1994-12-14 Enviropower Oy Method and reactor for treating process gas
NL1001555C2 (en) * 1995-10-27 1997-05-02 Biomass Technology Group B V Catalytically producing combustible gases, e.g., for generating energy
EP0801218A1 (en) * 1996-04-09 1997-10-15 FINMECCANICA S.p.A. Method and system of producing and utilizing fuel gases, in particular gases obtained from biomasses or refuse
WO2010037465A1 (en) * 2008-09-30 2010-04-08 Uhde Gmbh Hot gas purification
WO2012150871A1 (en) * 2011-05-03 2012-11-08 FRÂNCU, Bogdan-Sabin Procedure and installation for plasma heat treatment of a gas mixture

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SE8605211L (en) * 1986-12-04 1988-06-05 Skf Steel Eng Ab SET TO MAKE A GAS EMERGENCY FOR ENERGY PRODUCTION
NO174471C (en) * 1991-12-12 1994-05-11 Kvaerner Eng Method of preventing and removing fouling by pyrolytic cleavage of hydrocarbons
AU2006254672A1 (en) * 2005-06-03 2006-12-07 Plasco Energy Group Inc. A system for the conversion of carbonaceous feedstocks to a gas of a specified composition
KR101570882B1 (en) * 2009-08-04 2015-11-23 에스케이이노베이션 주식회사 Method for gasification of carbon containing material comprising methane decomposition and conversion of carbon dioxide
US9611437B2 (en) * 2010-01-12 2017-04-04 Lummus Technology Inc. Producing low methane syngas from a two-stage gasifier
EP3212566B1 (en) 2014-10-31 2021-03-10 Caphenia GmbH Method and plant for the production of synthesis gas
CN104629779A (en) * 2014-12-12 2015-05-20 中山大学 Process for producing synthetic gas from urban garbage by virtue of combination of pyrolysis and plasma
WO2023155974A1 (en) 2022-02-15 2023-08-24 Universität Stuttgart Solid plasma reactor and method of operating a fixed bed reactor
WO2023155975A1 (en) 2022-02-15 2023-08-24 Universität Stuttgart Process and device for obtaining carbon monoxide from atmospheric carbon dioxide, using a solid-plasma reactor

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1457862A (en) * 1974-05-10 1976-12-08 Centre Rech Metallurgique Producing hot reducing gas
GB1475731A (en) * 1973-03-26 1977-06-01 Skf Ind Trading & Dev Method of producing reduction gas
GB2008613A (en) * 1977-11-15 1979-06-06 Babcock Krauss Maffei Ind Pyrolysis of refuse
GB1566970A (en) * 1976-08-26 1980-05-08 Didier Eng Process for the treatment of coke-oven gas

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FR948266A (en) * 1946-06-24 1949-07-27 Nat Smelting Co Ltd Process for removing sulfur compounds from gases
US2701757A (en) * 1946-12-17 1955-02-08 Texaco Development Corp Process of making synthesis gas
SE371453C (en) * 1973-03-26 1978-01-12 Skf Ind Trading & Dev KIT FOR PRODUCTION OF REDUCTION GAS
BE815963A (en) * 1974-06-05 1974-09-30 HOT REDUCING GAS MANUFACTURING PROCESS.
US4123502A (en) * 1975-02-06 1978-10-31 Heinz Holter Process for the purification of gas generated in the pressure gasification of coal
DE2532197C3 (en) * 1975-07-18 1980-05-22 Metallgesellschaft Ag, 6000 Frankfurt Process for the production of synthesis gases
NL8302281A (en) * 1983-06-28 1985-01-16 Shell Int Research PROCESS FOR PREPARING A CARBON MONOXIDE AND HYDROGEN-CONTAINING GAS.
US4606761A (en) * 1983-11-29 1986-08-19 Union Steel Corp. (of So. Africa) Ltd. Reduction of metal compounds
FR2559776B1 (en) * 1984-02-16 1987-07-17 Creusot Loire SYNTHESIS GAS PRODUCTION PROCESS
SE453920B (en) * 1985-03-01 1988-03-14 Skf Steel Eng Ab SET AND DEVICE FOR GASING OF FOSSIL FUEL AND REFORM OF GAS FUEL

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1475731A (en) * 1973-03-26 1977-06-01 Skf Ind Trading & Dev Method of producing reduction gas
GB1457862A (en) * 1974-05-10 1976-12-08 Centre Rech Metallurgique Producing hot reducing gas
GB1566970A (en) * 1976-08-26 1980-05-08 Didier Eng Process for the treatment of coke-oven gas
GB2008613A (en) * 1977-11-15 1979-06-06 Babcock Krauss Maffei Ind Pyrolysis of refuse

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0310584A2 (en) * 1987-10-02 1989-04-05 TPS Termiska Processer Aktiebolag Refining of raw gas
EP0310584A3 (en) * 1987-10-02 1990-03-14 Studsvik Ab Refining of raw gas
US5213587A (en) * 1987-10-02 1993-05-25 Studsvik Ab Refining of raw gas
US4880439A (en) * 1988-05-05 1989-11-14 Texaco Inc. High temperature desulfurization of synthesis gas
EP0628621A2 (en) * 1993-06-11 1994-12-14 Enviropower Oy Method and reactor for treating process gas
EP0628621A3 (en) * 1993-06-11 1995-02-15 Enviropower Oy Method and reactor for treating process gas.
US5562744A (en) * 1993-06-11 1996-10-08 Enviropower Oy Method for treating process gas
NL1001555C2 (en) * 1995-10-27 1997-05-02 Biomass Technology Group B V Catalytically producing combustible gases, e.g., for generating energy
EP0801218A1 (en) * 1996-04-09 1997-10-15 FINMECCANICA S.p.A. Method and system of producing and utilizing fuel gases, in particular gases obtained from biomasses or refuse
WO2010037465A1 (en) * 2008-09-30 2010-04-08 Uhde Gmbh Hot gas purification
US8512444B2 (en) 2008-09-30 2013-08-20 Thyssenkrupp Uhde Gmbh Hot gas purification
WO2012150871A1 (en) * 2011-05-03 2012-11-08 FRÂNCU, Bogdan-Sabin Procedure and installation for plasma heat treatment of a gas mixture

Also Published As

Publication number Publication date
SE457355B (en) 1988-12-19
ATA256086A (en) 1992-12-15
AT396366B (en) 1993-08-25
IT8621793A0 (en) 1986-09-23
AU589997B2 (en) 1989-10-26
FI863726A0 (en) 1986-09-15
CA1309589C (en) 1992-11-03
BE905480A (en) 1987-01-16
AU6258286A (en) 1987-03-26
IT1213497B (en) 1989-12-20
GB2180849B (en) 1989-12-28
DE3631015A1 (en) 1987-04-16
JPS6274993A (en) 1987-04-06
FR2587717B1 (en) 1990-03-02
FI863726A (en) 1987-03-26
SE8504439D0 (en) 1985-09-25
IL80027A0 (en) 1986-12-31
SE8504439L (en) 1987-03-26
JP2509192B2 (en) 1996-06-19
BR8701328A (en) 1988-09-27
FR2587717A1 (en) 1987-03-27
GB8622866D0 (en) 1986-10-29
DE3631015C2 (en) 1988-10-06

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PCNP Patent ceased through non-payment of renewal fee

Effective date: 19990923