GB972140A - Removal of acidic gases from gaseous mixtures - Google Patents
Removal of acidic gases from gaseous mixturesInfo
- Publication number
- GB972140A GB972140A GB4590861A GB4590861A GB972140A GB 972140 A GB972140 A GB 972140A GB 4590861 A GB4590861 A GB 4590861A GB 4590861 A GB4590861 A GB 4590861A GB 972140 A GB972140 A GB 972140A
- Authority
- GB
- United Kingdom
- Prior art keywords
- absorbent
- formamide
- amine
- stripping
- recovered
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C7/00—Purification; Separation; Use of additives
- C07C7/11—Purification; Separation; Use of additives by absorption, i.e. purification or separation of gaseous hydrocarbons with the aid of liquids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10K—PURIFYING OR MODIFYING THE CHEMICAL COMPOSITION OF COMBUSTIBLE GASES CONTAINING CARBON MONOXIDE
- C10K1/00—Purifying combustible gases containing carbon monoxide
- C10K1/08—Purifying combustible gases containing carbon monoxide by washing with liquids; Reviving the used wash liquors
- C10K1/16—Purifying combustible gases containing carbon monoxide by washing with liquids; Reviving the used wash liquors with non-aqueous liquids
Abstract
A gas containing hydrocarbons, e.g. natural, refinery or flue gas is purified to remove acidic gases, e.g. H2S, CCS or CO2, by contact with a liquid mixture of (a) an amine having a basic dissociation constant pKb at 25 DEG C. of 3-14, and (b) an aliphatic carboxylic acid amide, a cyclotetramethylene sulphone or derivative thereof and/or a perhalocarbon. The liquid absorbent may comprise by weight, 7.5-70% of amine, e.g. ethanolamine, diethanolamine, di-isopropanolamine, dimethylamine, methyl ethyl amine, phenyl ethyl amine, 2,4-phenylene diamine or methoxy ethyl diamine, the balance being constituent (b) and if desired up to 15% of water. Constituent (b) may be sulpholane, containing up to 4 alkyl substituents if desired, dimethylformamide, methyl ethyl formamide, diethylformamide, propyl ethyl formamide, dibutyl formamide, dimethylacetamide, methyl ethyl acetamide, formamide, acetamide, perfluoro ethane, perfluoro butane or perchloro propane. The contact is effected in a countercurrent absorber at 7-70 kg./cm.2 absolute and 25-135 DEG C. The absorbent is recovered by removing acidic gases by stripping at 112-190 DEG C. and 1-3.5 kg./cm.2 absolute. If preferred the absorbent may first be subjected to flashing, e.g. at 1.15-8 kg./cm.2 abs. and gasoline hydrocarbons may be recovered from the gases so released by absorption in a sponge oil. Part of the absorbent after flashing may be recycled without further stripping to the absorption column. Preferably part of the stripped absorbent, e.g. 1-4% of the total, is dried by stripping and returned to the absorption column above the point of entry of the main absorbent to dry the gas. Sulphur is obtained from hydrogen sulphide recovered from the absorbent by the Claus process or alternatively sulphur dioxide is also passed into the absorption column where it reacts with the hydrogen sulphide to give sulphur recovered as a solid in the absorbent.ALSO:A gas containing hydrocarbons, e.g. natural, refinery or flue gas is purified to remove acidic gases, e.g. H2S, COS or CO2 by contact with a liquid mixture of (a) an amine having a basic dissociation constant pKb at 25 DEG C. of 3-14 and (b) an aliphatic carboxylic acid amide, a cyclotetramethylene sulphone or derivative thereof and/or a perhalocarbon. The liquid absorbent may comprise by weight, 7.5-70% of amine, e.g. ethanolamine, diethanolamine, di-isopropanolamine, dimethylamine, methyl ethylamine, phenyl ethyl amine, 2,4-phenylene diamine or methoxy ethyl diamine, the balance being constituent (b) and if desired up to 15% of water. Constituent (b) may be sulpholane, containing up to 4 alkyl substituents if desired, dimethylformamide, methyl ethyl formamide, diethylformamide, propyl ethyl formamide, dibutyl formamide, dimethylacetamide, methyl ethyl acetamide, formamide, acetamide, perfluoro ethane, perfluoro butane or perchloro propane. The contact is effected in a counter-current absorber at 7-70 kg./cm.2 absolute and 25-135 DEG C. The absorbent is recovered by removing acidic gases by stripping at 112-190 DEG C. and 1-3.5 kg./cm.2 absolute. If preferred, the absorbent may first be subjected to flashing, e.g. at 1.15-8 kg./cm.2 abs. and gasoline hydrocarbons may be recovered from the gases so released by absorption in a sponge oil. Part of the absorbent after flashing may be recycled without further stripping to the absorption column. Preferably, part of the stripped absorbent, e.g. 1-4% of the total, is dried by stripping and returned to the absorption column above the point of entry of the main absorbent to dry the gas.ALSO:A gas containing hydrocarbons, e.g. natural, refinery or flue gas, is purified to remove acidic gases, e.g. H2S, COS or CO2, by contact with a liquid mixture of (a) an amine having a basic dissociation constant pKb at 25 DEG C. of 3-14 and (b) an aliphatic carboxylic acid amide, a cyclotetramethylene sulphone or derivative thereof and/or a perhalocarbon. The liquid absorbent may comprise by weight, 7,5-70% of amine, e.g. ethanolamine, diethanolamine, di-isopropanolamine, dimethylamine, methyl ethyl amine, phenyl ethyl amine, 2,4-phenylene diamine or methoxy ethyl diamine, the balance being constituent (b) and if desired up to 15% of water. Constituent (b) may be sulpholane, containing up to 4 alkyl substituents if desired, dimethylformamide, methyl ethyl formamide, diethylformamide, propyl ethyl formamide, dibutyl formamide, dimethylacetamide, methyl ethyl acetamide, formamide, acetamide, perfluoro ethane, perfluoro butane or perchloro propane. The contact is effected in a counter-current absorber at 7-70 Kg./cm.2 absolute and 25-135 DEG C. The absorbent is recovered by removing acidic gases by stripping at 112-190 DEG C. and 1-3,5 kg./cm.2 absolute. If preferred the absorbent may first be subjected to flashing, e.g. at 1,15-8 Kg./cm.2 absolute and gasoline hydrocarbons may be recovered from the gases so released by absorption in a sponge oil. Part of the absorbent after flashing may be recycled without further stripping to the absorption column. Preferably part of the stripped absorbent, e.g. 1-4% of the total, is dried by stripping and returned to the absorption column above the point of entry of the main absorbent to dry the gas.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US78162A US3161461A (en) | 1960-12-23 | 1960-12-23 | Method of removing acidic gases from gaseous mixtures |
US13138561A | 1961-08-14 | 1961-08-14 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB972140A true GB972140A (en) | 1964-10-07 |
Family
ID=26760172
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB4590861A Expired GB972140A (en) | 1960-12-23 | 1961-12-21 | Removal of acidic gases from gaseous mixtures |
Country Status (5)
Country | Link |
---|---|
DE (1) | DE1276283B (en) |
DK (1) | DK107246C (en) |
GB (1) | GB972140A (en) |
MY (1) | MY6500109A (en) |
NL (1) | NL272877A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2380061A1 (en) * | 1977-02-14 | 1978-09-08 | Exxon Research Engineering Co | PROCESS FOR THE ELIMINATION OF ACID GASES PRESENT IN GAS MIXTURES, AND LIQUID ABSORBENTS FOR THIS ELIMINATION |
FR2469381A1 (en) * | 1979-11-12 | 1981-05-22 | Union Rheinische Braunkohlen | PROCESS FOR OBTAINING PURE HYDROGEN SULFIDE |
US7250450B2 (en) | 2002-06-05 | 2007-07-31 | Shell Oil Company | Process for the production of hydrocarbons from gaseous hydrocarbonaceous feed |
WO2011048066A1 (en) | 2009-10-21 | 2011-04-28 | Shell Internationale Research Maatschappij B.V. | Method & apparatus for processing fischer-tropsch off-gas |
WO2013017700A1 (en) | 2011-08-04 | 2013-02-07 | Shell Internationale Research Maatschappij B.V. | Process for producing hydrocarbons from syngas |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE549556C (en) * | 1928-12-04 | 1932-04-29 | Girdler Corp | Process for removing acidic gases such as carbon dioxide, sulfur dioxide, hydrogen sulfide and the like from gas mixtures |
DE620932C (en) * | 1934-02-02 | 1935-10-30 | I G Farbenindustrie Akt Ges | Process for removing weak gaseous acids from gases |
-
0
- NL NL272877D patent/NL272877A/xx unknown
-
1961
- 1961-12-21 DK DK512661A patent/DK107246C/en active
- 1961-12-21 GB GB4590861A patent/GB972140A/en not_active Expired
- 1961-12-21 DE DES77317A patent/DE1276283B/en active Granted
-
1965
- 1965-12-31 MY MY6500109A patent/MY6500109A/en unknown
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2380061A1 (en) * | 1977-02-14 | 1978-09-08 | Exxon Research Engineering Co | PROCESS FOR THE ELIMINATION OF ACID GASES PRESENT IN GAS MIXTURES, AND LIQUID ABSORBENTS FOR THIS ELIMINATION |
FR2469381A1 (en) * | 1979-11-12 | 1981-05-22 | Union Rheinische Braunkohlen | PROCESS FOR OBTAINING PURE HYDROGEN SULFIDE |
US7250450B2 (en) | 2002-06-05 | 2007-07-31 | Shell Oil Company | Process for the production of hydrocarbons from gaseous hydrocarbonaceous feed |
WO2011048066A1 (en) | 2009-10-21 | 2011-04-28 | Shell Internationale Research Maatschappij B.V. | Method & apparatus for processing fischer-tropsch off-gas |
WO2013017700A1 (en) | 2011-08-04 | 2013-02-07 | Shell Internationale Research Maatschappij B.V. | Process for producing hydrocarbons from syngas |
Also Published As
Publication number | Publication date |
---|---|
DK107246C (en) | 1967-05-08 |
NL272877A (en) | |
DE1276283C2 (en) | 1969-04-17 |
DE1276283B (en) | 1968-08-29 |
MY6500109A (en) | 1965-12-31 |
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