EP0515446A1 - Verfahren zur erzeugung von kohlenmonoxid - Google Patents

Verfahren zur erzeugung von kohlenmonoxid

Info

Publication number
EP0515446A1
EP0515446A1 EP91903849A EP91903849A EP0515446A1 EP 0515446 A1 EP0515446 A1 EP 0515446A1 EP 91903849 A EP91903849 A EP 91903849A EP 91903849 A EP91903849 A EP 91903849A EP 0515446 A1 EP0515446 A1 EP 0515446A1
Authority
EP
European Patent Office
Prior art keywords
gas
reforming stage
carbon dioxide
reforming
fed
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.)
Ceased
Application number
EP91903849A
Other languages
German (de)
English (en)
French (fr)
Inventor
Arno Czimczik
Manfred Schmitz-Goeb
Eckhard Friese
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Hitachi Zosen Inova Steinmueller GmbH
Original Assignee
L&C Steinmueller GmbH
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 L&C Steinmueller GmbH filed Critical L&C Steinmueller GmbH
Publication of EP0515446A1 publication Critical patent/EP0515446A1/de
Ceased legal-status Critical Current

Links

Classifications

    • 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
    • C01B3/34Production 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 by reaction of hydrocarbons with gasifying agents
    • C01B3/38Production 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 by reaction of hydrocarbons with gasifying agents using catalysts
    • C01B3/382Multi-step processes
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B32/00Carbon; Compounds thereof
    • C01B32/40Carbon monoxide

Definitions

  • the invention relates to a process for the production of carbon monoxide, in which a mixture of hydrocarbon, preferably methane, and carbon dioxide is fed in the presence of a catalyst with the supply of heat to at least one reforming stage and carbon dioxide and hydrogen are separated from the reformed starting gas mixture.
  • the reforming stage consists of a radiation reformer to which combustion air and fuel are fed for heating.
  • the carbon dioxide content from the exhaust gases from the reformer heating is recovered for the reforming process, as is the residual carbon dioxide content remaining in the product gas.
  • the nitrogen content from the exhaust gases is removed as a by-product.
  • Heat is removed from the reforming process at various points by coolers.
  • This object is achieved in that the gas mixture is fed to a convectively heated first reforming stage, the starting gas of the first reforming stage is fed together with oxygen to an autothermal second reforming stage, and the starting gas of the second reforming stage is fed to the convectively heated reforming stage as heating gas.
  • the heat generated in the autothermal reforming stage is used for the process itself, since it is used to heat the first reforming stage via the heating gas.
  • Convectionally heated reforming stages are known per se. They preferably have a large number of canned tubes with an outer tube flushed with a heating gas and an inner tube serving for gas recirculation, the space between the outer tube and inner tube being filled with a catalyst (cf., for example, the applicant's prospectus: "Plant and Apparatus construction - components and circuits! "(1986) page 31).
  • Autothermal reformers which are often used as secondary reformers, are also known per se.
  • NH3 synthesis z. B first subjected to a steam refor ier process the feed gas in a primary reformer.
  • the starting gas from the primary reformer with a relatively high residual methane content is then mixed with air in an autothermal reformer serving as a secondary reformer via a mixing device (burner) and then passed over a bed of catalyst.
  • the secondary reform stage serves to introduce nitrogen into the synthesis gas (see DE-Z. "Chemiker-Zeitung” (1972) page 141, right column).
  • the second reforming stage is additionally supplied with carbon dioxide.
  • the heat content of the gases emerging from the convectively heated reforming stage is still sufficiently large, it is expedient to preheat at least one of the feed gases and / or at least one of the return gases by heat exchange with the starting gas of the second reforming stage, i.e. H. also to integrate the remaining waste heat in the process for the production of carbon monoxide un as in the known process management in external processes, for. B. for steam generation.
  • a mixture of essentially methane (CH *) and carbon dioxide (CO2) is fed via line 1, in which a heat exchanger 2 is arranged, to a convectively heated reformer 3.
  • the preheated gas mixture flows through a can filled with a catalyst.
  • the starting gas of the reformer 3 with high proportions of carbon monoxide, carbon dioxide, water vapor and hydrogen, and a residual methane content is fed via line 4 to an autothermal reformer 5.
  • the autothermal reformer 5 we Via a line 7 oxygen (O2) supplied.
  • the output gas of the reformer 3 supplied via line 4 is further reformed here in an autothermal process in order to substantially reduce the residual methane content.
  • the starting gas of the autothermal reformer 5 is fed via a line 8 as the heating gas to the convectively heated reformer 3, in which it flows around the can from the outside.
  • the output gas of the reformer 3 is fed via a line 9, in which the heat exchanger 2 and a further heat exchanger 6 are arranged, to a water vapor separator 10, from which the separated water is drawn off via a line 11.
  • the synthesis gas which now consists of a mixture of carbon monoxide, carbon dioxide and hydrogen and possibly a very small proportion of residual methane, is then fed via line 12 to a carbon dioxide scrubber 13.
  • the washed-out carbon dioxide is returned to line 1 as a return gas via a line 14 and / or is fed to line 4 and thus to the autothermal reformer 5 via a line 15 led via the heat exchanger 6.
  • the gas freed from carbon dioxide is fed via line 16 to a hydrogen separator 17; the gas freed from hydrogen is withdrawn as product gas via line 18.
  • the separated hydrogen can be fed via lines 19 and 20 to the reformers 3 and 5 as recycle gas.
  • the heat exchanger 21 shown in dashed lines in the figure is intended to show that preheating of the recycled hydrogen by the starting gas of the first reforming stage could also be considered if necessary.
  • gas cleaning stages 10, 13 and 17 are used to set an im essential carbon monoxide-containing product gas with desired proportions of water vapor, carbon dioxide and hydrogen is possible; if necessary, methane can also be fed via a line 22 to the autothermal reformer 5, which is preheated together with the carbon dioxide in the heat exchanger 6.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Inorganic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Combustion & Propulsion (AREA)
  • Hydrogen, Water And Hydrids (AREA)
EP91903849A 1990-02-16 1991-02-14 Verfahren zur erzeugung von kohlenmonoxid Ceased EP0515446A1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE4004869 1990-02-16
DE4004869A DE4004869C1 (ja) 1990-02-16 1990-02-16

Publications (1)

Publication Number Publication Date
EP0515446A1 true EP0515446A1 (de) 1992-12-02

Family

ID=6400314

Family Applications (1)

Application Number Title Priority Date Filing Date
EP91903849A Ceased EP0515446A1 (de) 1990-02-16 1991-02-14 Verfahren zur erzeugung von kohlenmonoxid

Country Status (3)

Country Link
EP (1) EP0515446A1 (ja)
DE (1) DE4004869C1 (ja)
WO (1) WO1991012200A1 (ja)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5102645A (en) * 1990-06-21 1992-04-07 Liquid Carbonic Corporation Method for manufacture of high purity carbon monoxide
GB2592681B (en) * 2020-03-06 2022-06-22 Reinertsen New Energy As Hydrogen and/or ammonia production process

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3549335A (en) * 1965-10-22 1970-12-22 Braun & Co C F Autothermal reactor
US3958951A (en) * 1974-04-09 1976-05-25 Stone & Webster Engineering Corporation Convective power reformer equipment and system
US4162290A (en) * 1976-11-19 1979-07-24 Pullman Incorporated Parallel steam reformers to provide low energy process
US4182746A (en) * 1978-06-16 1980-01-08 Atlantic Richfield Company Carbon monoxide manufacture
DE3501459A1 (de) * 1985-01-17 1986-07-17 Linde Ag, 6200 Wiesbaden Verfahren zur erzeugung von h(pfeil abwaerts)2(pfeil abwaerts)/co-synthesegas und co
EP0194067B2 (en) * 1985-03-05 1994-05-11 Imperial Chemical Industries Plc Steam reforming hydrocarbons
GB8514344D0 (en) * 1985-06-06 1985-07-10 Ici Plc Catalyst support
EP0291857A3 (en) * 1987-05-18 1990-07-18 Air Products And Chemicals, Inc. Method of carbon monoxide production
US4861351A (en) * 1987-09-16 1989-08-29 Air Products And Chemicals, Inc. Production of hydrogen and carbon monoxide

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO9112200A1 *

Also Published As

Publication number Publication date
DE4004869C1 (ja) 1991-02-07
WO1991012200A1 (de) 1991-08-22

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Legal Events

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