WO2003072225A1 - Verfahren zur entfernung von merkaptan aus rohgas - Google Patents

Verfahren zur entfernung von merkaptan aus rohgas Download PDF

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Publication number
WO2003072225A1
WO2003072225A1 PCT/EP2003/000582 EP0300582W WO03072225A1 WO 2003072225 A1 WO2003072225 A1 WO 2003072225A1 EP 0300582 W EP0300582 W EP 0300582W WO 03072225 A1 WO03072225 A1 WO 03072225A1
Authority
WO
WIPO (PCT)
Prior art keywords
gas
absorption
fed
mercaptan
claus
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
PCT/EP2003/000582
Other languages
German (de)
English (en)
French (fr)
Inventor
Karin Huder
Max-Michael Weiss
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.)
Air Liquide Global E&C Solutions Germany GmbH
Original Assignee
Lurgi 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 Lurgi GmbH filed Critical Lurgi GmbH
Priority to JP2003570963A priority Critical patent/JP4508653B2/ja
Priority to US10/505,493 priority patent/US7189282B2/en
Priority to AU2003248333A priority patent/AU2003248333A1/en
Priority to DE50302133T priority patent/DE50302133D1/de
Priority to EP03742865A priority patent/EP1480733B1/de
Priority to KR1020047013337A priority patent/KR100950828B1/ko
Publication of WO2003072225A1 publication Critical patent/WO2003072225A1/de
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • 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 OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
    • C10L3/00—Gaseous fuels; Natural gas; Synthetic natural gas obtained by processes not covered by subclass C10G, C10K; Liquefied petroleum gas
    • C10L3/06—Natural gas; Synthetic natural gas obtained by processes not covered by C10G, C10K3/02 or C10K3/04
    • C10L3/10—Working-up natural gas or synthetic natural gas
    • C10L3/101—Removal of contaminants
    • C10L3/102—Removal of contaminants of acid contaminants
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/14—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by absorption
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/02—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/14—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by absorption
    • B01D53/1406—Multiple stage absorption
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/14—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by absorption
    • B01D53/1456—Removing acid components
    • B01D53/1462—Removing mixtures of hydrogen sulfide and carbon dioxide
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B17/00—Sulfur; Compounds thereof
    • C01B17/02—Preparation of sulfur; Purification
    • C01B17/04—Preparation of sulfur; Purification from gaseous sulfur compounds including gaseous sulfides
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B17/00—Sulfur; Compounds thereof
    • C01B17/02—Preparation of sulfur; Purification
    • C01B17/04—Preparation of sulfur; Purification from gaseous sulfur compounds including gaseous sulfides
    • C01B17/0404—Preparation of sulfur; Purification from gaseous sulfur compounds including gaseous sulfides by processes comprising a dry catalytic conversion of hydrogen sulfide-containing gases, e.g. the Claus process
    • C01B17/0408—Pretreatment of the hydrogen sulfide containing gases
    • 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 OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
    • C10L3/00—Gaseous fuels; Natural gas; Synthetic natural gas obtained by processes not covered by subclass C10G, C10K; Liquefied petroleum gas
    • C10L3/06—Natural gas; Synthetic natural gas obtained by processes not covered by C10G, C10K3/02 or C10K3/04
    • C10L3/10—Working-up natural gas or synthetic natural gas
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D2257/00—Components to be removed
    • B01D2257/30—Sulfur compounds
    • B01D2257/304—Hydrogen sulfide
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D2257/00—Components to be removed
    • B01D2257/30—Sulfur compounds
    • B01D2257/306—Organic sulfur compounds, e.g. mercaptans
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D2257/00—Components to be removed
    • B01D2257/50—Carbon oxides
    • B01D2257/504—Carbon dioxide
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02C—CAPTURE, STORAGE, SEQUESTRATION OR DISPOSAL OF GREENHOUSE GASES [GHG]
    • Y02C20/00—Capture or disposal of greenhouse gases
    • Y02C20/40—Capture or disposal of greenhouse gases of CO2
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00—Technologies relating to chemical industry
    • Y02P20/151—Reduction of greenhouse gas [GHG] emissions, e.g. CO2

Definitions

  • the invention relates to a method for purifying gas, in particular gas containing hydrocarbons, such as natural gas, which is contaminated with sulfur in the form of H 2 S and mercaptan and C0 2 .
  • the document WO 97/26069 describes a process for the purification of carbon dioxide and sulfur-containing gases, in which there are sulfur-contaminated impurities in the form of mercaptans and H 2 S.
  • the sulfur-containing impurities are removed from the gas in order to generate a clean gas stream and an acid gas stream, the acid gas being hydrogenated in order to convert a larger proportion of mercaptans to H 2 S.
  • the hydrogenated acid gas is introduced into a second absorption / regeneration plant, in which the acid gas is separated into a H 2 S-rich first gas stream, which is introduced into a Claus plant, and a second H 2 S-poor gas flow, which is used for afterburning to be led.
  • the Claus plant is followed by a tail gas aftertreatment in which the H 2 S is further reduced and an H 2 S-rich gas is withdrawn.
  • a disadvantage of this process is the insufficient amount of sulfur and mercaptans that can be removed from the gas. According to the prior art, it is only possible with great effort to remove more than 95% by weight of the sulfur from the raw gas.
  • the invention has for its object to provide an improved process for the purification of hydrocarbon-containing gas, in which the undesirable sulfur-containing substances in the form of H 2 S and mercaptan are removed.
  • the object is achieved in that raw gas is passed into an absorption and regeneration column and washed there, three gas streams being drawn off from this absorption and regeneration column, a first exhaust gas stream being passed to a Claus plant and a second sour gas stream having a lower rate H 2 S concentration of 10 - 30 vol% is passed into another absorption system, and a third gas stream, the valuable gas with the mercaptans, is cooled and fed to an adsorption system, that a sweet gas is drawn off from this adsorption system and a gas stream containing a mercaptan is washed is subjected.
  • a physical wash for example a purisol plant, is preferably used as the wash, with which a small amount of gas with a high mercaptan concentration is introduced into the Claus plant and a part of the adsorbed valuable gas from the regeneration of the adsorption plant is recovered as fuel gas.
  • the mercaptan gas is completely burned in the Claus plant.
  • the Claus plant can be made smaller, since the sour gas stream has a higher concentration of H 2 S.
  • the H 2 S-containing solution is drawn off from the absorption system, which is arranged after the hydrogenation of the residual Claus gas, and introduced into the absorption system for the strengthening of the acid gas.
  • the degree of sulfur recovery is increased by passing the gas from the absorption of the fortification into the hydrogenation to convert sulfur components to H 2 S and then into the absorption of the tail gas aftertreatment.
  • Raw gas is fed via line (1) into a first wash consisting of an absorption and a
  • Regeneration column (2) passed and washed there.
  • This exhaust gas stream (5) consists mainly of up to 80 vol .-% hydrocarbon and up to 20 vol .-% of C0 2 with small amounts of mercaptans (up to 0.3 vol .-%) and H 2 S (up to 5 vol%).
  • a second sour gas stream (4) with a low H 2 S concentration with up to 30% by volume H 2 S is passed into a further absorption system (15) and is strengthened there with an unloaded solvent from lines (26) and (27).
  • the solvent (16) loaded with H 2 S is introduced from the absorption system (15) into a regeneration system (17).
  • Regeneration (17) turns sour gas with a high H 2 S concentration of up to 60 vol.%
  • the mercaptan-containing gas stream (10) is subjected to a physical wash, from which the co-adsorbed valuable gas is fed via line (12)
  • Fuel gas is recovered, and the highly concentrated mercaptan gas is fed to the Claus plant (14) via line (13).
  • the Merkaptanstrom is in the regeneration of the
  • the amount is small, but with a very high one Merkaptan concentration from 10% by volume to 60% by volume.
  • the mercaptan is completely burned in the Claus plant (14).
  • the resulting SO 2 is converted to sulfur with the H 2 S from the acid gas in line (19).
  • the resulting liquid sulfur is withdrawn via line (21) and sent for further use. A high degree of sulfur recovery is achieved.
  • the Claus plant (14) is a known plant which consists of an incinerator and several catalytic reactors for carrying out the reaction.
  • Claus residual gas which, in addition to uncondensed elemental sulfur, contains unreacted sulfur dioxide and H 2 S.
  • This residual gas is withdrawn via line (20) and is subjected to an aftertreatment in order to increase the degree of sulfur recovery.
  • the residual Claus gas is fed via line (20) to a hydrogenation system (22), which is also supplied with the gas via line (18) from the absorption system (15).
  • H 2 S In the hydrogenation S0 2 is converted to H 2 S and fed to an absorption system (24) via line (23).
  • a solution is fed from the absorption system (24) via line (26) into the strengthening absorption (15) for further absorption of H 2 S.
  • the remaining H 2 S-containing gas is withdrawn via line (25) from the absorption system (24) and fed to a combustion.
  • raw gas is fed via line (1) into an absorption and regeneration column (2) and washed there.
  • the first exhaust gas stream (5) from the regeneration which consists of approx. 76 vol .-% hydrocarbon and approx. 13 Vo! .-% CO 2 with small amounts of mercaptans and H 2 S, is fed directly into a Claus plant (14 ) headed.
  • a second sour gas stream (4) with a low H 2 S concentration (20.5% by volume) is passed into an absorption system (15) and is strengthened there with a solvent from line (26) and (27) which is not or hardly loaded.
  • the solvent (16) loaded with H 2 S is introduced from the absorption system (15) into a regeneration system (17).
  • the gas with around 96% by volume of CO 2 and 0.2% by volume of mercaptan from the absorption system (15) is fed to a hydrogenation (22) via line (18).
  • sour gas with a high H 2 S concentration 43.8% by volume is passed via line (19) into the Claus plant (14).
  • a third gas stream (3) with a mercaptan content of around 0.01% by volume is drawn off, cooled (6) and fed to an adsorption (8) via line (7).
  • the valuable gas is fed via line (9) to further processes, for example liquefaction.
  • the mercaptan-containing gas stream is subjected to a physical wash, from which part of the valuable gas is recovered as fuel gas via line (12), and the highly concentrated mercaptan gas is fed to the Claus system (14) via line (13).
  • the mercaptan current is obtained in the regeneration of the purisol solvent. The amount is small, but with a very high mercaptan concentration of around 54 vol.%.
  • the mercaptan is completely burned in the Claus plant (14).
  • the resulting S0 2 is converted to sulfur with the H 2 S from the acid gas in line (19).
  • the resulting liquid sulfur is withdrawn via line (21) and sent for further use.
  • the residual gas of the Claus plant mainly consists of the components C0 2 , N 2 and H 2 0 and is withdrawn via line (20).

Landscapes

  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Analytical Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Treating Waste Gases (AREA)
  • Gas Separation By Absorption (AREA)
  • Industrial Gases (AREA)
  • Separation By Low-Temperature Treatments (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
PCT/EP2003/000582 2002-02-26 2003-01-22 Verfahren zur entfernung von merkaptan aus rohgas Ceased WO2003072225A1 (de)

Priority Applications (6)

Application Number Priority Date Filing Date Title
JP2003570963A JP4508653B2 (ja) 2002-02-26 2003-01-22 未精製ガスからメルカプタンを除去する方法
US10/505,493 US7189282B2 (en) 2002-02-26 2003-01-22 Method for eliminating mercaptan from crude gas
AU2003248333A AU2003248333A1 (en) 2002-02-26 2003-01-22 Method for eliminating mercaptan from crude gas
DE50302133T DE50302133D1 (de) 2002-02-26 2003-01-22 Verfahren zur entfernung von merkaptan aus rohgas
EP03742865A EP1480733B1 (de) 2002-02-26 2003-01-22 Verfahren zur entfernung von merkaptan aus rohgas
KR1020047013337A KR100950828B1 (ko) 2002-02-26 2003-01-22 미정제 가스로부터 메르캅탄을 제거하는 방법

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE10208253.7 2002-02-26
DE10208253A DE10208253A1 (de) 2002-02-26 2002-02-26 Verfahren zur Entfernung von Merkaptan aus Rohgas

Publications (1)

Publication Number Publication Date
WO2003072225A1 true WO2003072225A1 (de) 2003-09-04

Family

ID=27674991

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2003/000582 Ceased WO2003072225A1 (de) 2002-02-26 2003-01-22 Verfahren zur entfernung von merkaptan aus rohgas

Country Status (8)

Country Link
US (1) US7189282B2 (enExample)
EP (1) EP1480733B1 (enExample)
JP (1) JP4508653B2 (enExample)
KR (1) KR100950828B1 (enExample)
AT (1) ATE314882T1 (enExample)
AU (1) AU2003248333A1 (enExample)
DE (2) DE10208253A1 (enExample)
WO (1) WO2003072225A1 (enExample)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE10357324A1 (de) * 2003-12-05 2005-07-21 Uhde Gmbh Verfahren zur Verschiebung von Sauergasanteilen innerhalb eines Erdgasnetzwerkes
EP2402068A1 (en) * 2004-01-20 2012-01-04 Fluor Technologies Corporation Methods and configurations for acid gas enrichment

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE10219900B4 (de) * 2002-05-03 2004-08-26 Lurgi Ag Verfahren zur Reinigung von kohlenwasserstoffhaltigem Gas
WO2006113935A2 (en) * 2005-04-20 2006-10-26 Fluor Technologies Corporation Configurations and methods for claus plant operation with variable sulfur content
JP4845438B2 (ja) * 2005-07-08 2011-12-28 千代田化工建設株式会社 天然ガスからの硫黄化合物の除去方法
US8444943B2 (en) 2010-04-30 2013-05-21 Black & Veatch Corporation Methods and apparatus for sulfur recovery from acid gases
EP2869909A1 (en) * 2012-07-03 2015-05-13 Shell Internationale Research Maatschappij B.V. Process for deep contaminent removal of gas streams
DE102012017045A1 (de) * 2012-08-29 2014-05-15 Thyssenkrupp Uhde Gmbh Verfahren zur Wäsche von schwefelhaltigen Gasen mit einer im Kreislauf geführten ammoniakhaltigen Waschlösung
AR093896A1 (es) * 2012-12-10 2015-06-24 Total Sa Proceso integrado para recuperar co₂ natural de alta calidad de un gas sulfuroso que comprende h₂s y co₂, y dispositivo utilizado
CN104994933B (zh) * 2013-02-19 2017-03-15 西门子公司 用于处理气体流、尤其用于处理天然气流的设备和方法
US12480064B2 (en) 2021-11-19 2025-11-25 Petróleo Brasileiro S.A.—Petrobras Process for the removal of H2S from natural gas at high pressures by means of a PSA process
CN114225680A (zh) * 2021-12-16 2022-03-25 安徽华塑股份有限公司 用二氧化碳催化转化产物脱除窑炉尾气中氮氧化物的方法

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3989811A (en) * 1975-01-30 1976-11-02 Shell Oil Company Process for recovering sulfur from fuel gases containing hydrogen sulfide, carbon dioxide, and carbonyl sulfide
US4372925A (en) * 1980-03-31 1983-02-08 Shell Oil Company Process for the removal of acid gases from gas mixtures containing methane
US4552572A (en) * 1983-07-26 1985-11-12 Bechtel International Corporation Process for desulfurization of fuel gas
WO1997026069A1 (en) * 1996-01-19 1997-07-24 Stork Engineers & Contractors B.V. Method for removing sulfur-containing contaminants, aromatics and hydrocarbons from gas
WO1997026070A1 (en) * 1996-01-19 1997-07-24 Stork Engineers & Contractors B.V. Method for removing sulfur-containing contaminants, aromatics and hydrocarbons from gas

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DE3047830A1 (de) * 1980-12-18 1982-07-15 Linde Ag, 6200 Wiesbaden Verfahren zum reinigen eines gasstromes
US4397660A (en) * 1981-06-15 1983-08-09 Shell Oil Company Process for the removal of H2 S and CO2 from a gas mixture
US4957715A (en) * 1988-04-15 1990-09-18 Uop Gas treatment process
JPH06504949A (ja) * 1991-05-21 1994-06-09 エクソン　ケミカル　パテンツ　インコーポレイテッド ハイブリッド膜分離システムを用いる酸性ガスの処理
JP3823366B2 (ja) * 1996-03-23 2006-09-20 千代田化工建設株式会社 イオウ回収方法及びイオウ回収プラント
DE19933301A1 (de) * 1999-07-15 2001-01-18 Basf Ag Verfahren zum Entfernen von Mercaptanen aus Fluidströmen

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3989811A (en) * 1975-01-30 1976-11-02 Shell Oil Company Process for recovering sulfur from fuel gases containing hydrogen sulfide, carbon dioxide, and carbonyl sulfide
US4372925A (en) * 1980-03-31 1983-02-08 Shell Oil Company Process for the removal of acid gases from gas mixtures containing methane
US4552572A (en) * 1983-07-26 1985-11-12 Bechtel International Corporation Process for desulfurization of fuel gas
WO1997026069A1 (en) * 1996-01-19 1997-07-24 Stork Engineers & Contractors B.V. Method for removing sulfur-containing contaminants, aromatics and hydrocarbons from gas
WO1997026070A1 (en) * 1996-01-19 1997-07-24 Stork Engineers & Contractors B.V. Method for removing sulfur-containing contaminants, aromatics and hydrocarbons from gas

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE10357324A1 (de) * 2003-12-05 2005-07-21 Uhde Gmbh Verfahren zur Verschiebung von Sauergasanteilen innerhalb eines Erdgasnetzwerkes
DE10357324B4 (de) * 2003-12-05 2008-11-13 Uhde Gmbh Verfahren zur Verschiebung von Sauergasanteilen innerhalb eines Erdgasnetzwerkes
EP2402068A1 (en) * 2004-01-20 2012-01-04 Fluor Technologies Corporation Methods and configurations for acid gas enrichment
EP1720632B1 (en) * 2004-01-20 2016-01-13 Fluor Technologies Corporation Methods and configurations for acid gas enrichment

Also Published As

Publication number Publication date
ATE314882T1 (de) 2006-02-15
US7189282B2 (en) 2007-03-13
KR20040103950A (ko) 2004-12-09
EP1480733B1 (de) 2006-01-04
DE50302133D1 (de) 2006-03-30
AU2003248333A1 (en) 2003-09-09
KR100950828B1 (ko) 2010-04-02
JP4508653B2 (ja) 2010-07-21
US20050103194A1 (en) 2005-05-19
JP2005518271A (ja) 2005-06-23
DE10208253A1 (de) 2003-09-04
EP1480733A1 (de) 2004-12-01

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