GB1005096A - Process for the removal of hydrogen sulphide from gases - Google Patents
Process for the removal of hydrogen sulphide from gasesInfo
- Publication number
- GB1005096A GB1005096A GB1604963A GB1604963A GB1005096A GB 1005096 A GB1005096 A GB 1005096A GB 1604963 A GB1604963 A GB 1604963A GB 1604963 A GB1604963 A GB 1604963A GB 1005096 A GB1005096 A GB 1005096A
- Authority
- GB
- United Kingdom
- Prior art keywords
- solvent
- sulphone
- ferrous
- weight
- dimethyl
- 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
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 title abstract 13
- 239000007789 gas Substances 0.000 title abstract 7
- 238000000034 method Methods 0.000 title abstract 3
- 239000002904 solvent Substances 0.000 abstract 13
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 abstract 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 8
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 6
- 239000005864 Sulphur Substances 0.000 abstract 6
- 229910001448 ferrous ion Inorganic materials 0.000 abstract 6
- 125000001174 sulfone group Chemical group 0.000 abstract 6
- -1 methyl ethyl Chemical group 0.000 abstract 5
- 239000002738 chelating agent Substances 0.000 abstract 4
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 abstract 4
- 230000001590 oxidative effect Effects 0.000 abstract 4
- 238000010521 absorption reaction Methods 0.000 abstract 3
- 150000001735 carboxylic acids Chemical class 0.000 abstract 3
- QWUWMCYKGHVNAV-UHFFFAOYSA-N 1,2-dihydrostilbene Chemical group C=1C=CC=CC=1CCC1=CC=CC=C1 QWUWMCYKGHVNAV-UHFFFAOYSA-N 0.000 abstract 2
- DYGJDTCGUUMUBL-UHFFFAOYSA-N 2,3-dihydrothiophene 1,1-dioxide Chemical compound O=S1(=O)CCC=C1 DYGJDTCGUUMUBL-UHFFFAOYSA-N 0.000 abstract 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 abstract 2
- 229910002651 NO3 Inorganic materials 0.000 abstract 2
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 abstract 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- 150000007513 acids Chemical class 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 150000001413 amino acids Chemical class 0.000 abstract 2
- 238000006243 chemical reaction Methods 0.000 abstract 2
- 239000003795 chemical substances by application Substances 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 2
- 238000010494 dissociation reaction Methods 0.000 abstract 2
- 230000005593 dissociations Effects 0.000 abstract 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 abstract 2
- 229920000768 polyamine Polymers 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 238000006467 substitution reaction Methods 0.000 abstract 2
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 abstract 2
- 229910021653 sulphate ion Inorganic materials 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 238000009835 boiling Methods 0.000 abstract 1
- 150000001991 dicarboxylic acids Chemical class 0.000 abstract 1
- 229930195733 hydrocarbon Natural products 0.000 abstract 1
- 150000002430 hydrocarbons Chemical class 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000003345 natural gas Substances 0.000 abstract 1
- SIOXPEMLGUPBBT-UHFFFAOYSA-N picolinic acid Chemical class OC(=O)C1=CC=CC=N1 SIOXPEMLGUPBBT-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- 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
- B01D53/34—Chemical or biological purification of waste gases
- B01D53/46—Removing components of defined structure
- B01D53/48—Sulfur compounds
- B01D53/52—Hydrogen sulfide
- B01D53/523—Mixtures of hydrogen sulfide and sulfur oxides
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Biomedical Technology (AREA)
- Environmental & Geological Engineering (AREA)
- Analytical Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Treating Waste Gases (AREA)
Abstract
Gases, e.g. natural gas or refinery gas, are purified from hydrogen sulphide by absorption of the hydrogen sulphide in a solvent containing water, at least one sulphone, at least one ferrous salt and at least one chelating agent for ferrous ions, and the hydrogen sulphide-containing solvent is treated with SO2, whereby water and sulphur are formed. The water content of the solvent is preferably 2-20% by weight. The sulphone, at least 50% by weight, is preferably a hydrocarbyl sulphone, e.g. methyl ethyl, diethyl, di-n-propyl, dibenzyl or ditolyl sulphone, or tetrahydrothiophene-1,1-dioxide or 2,3-dihydrothiophene-1,1-dioxide, or substitution derivatives of these containing not more than four alkyl groups per molecule, e.g. the 2,3-dimethyl, 2,4-dimethyl, 2,5-dimethyl, 3-ethyl or 2-methyl-5-propyl derivatives of tetrahydrothiophene-1,1-dioxide. Hydroxyamino- or keto-sulphones may also be utilized. The ferrous salt, 0.5-10% by weight, may be ferrous nitrate, chloride or sulphate. The chelating agent, 0.1-5% by weight, or 0.1-1 molecule for each ferrous ion present, is any compound capable of forming one or more complexes with ferrous ions, the negative logarithm of the dissociation constant of the complexes being preferably in the range 0.2-10 in the temperature range - 1 to 150 DEG C., and suitable agents include alkyleneamine carboxylic acids, amine carboxylic acids, dicarboxylic acids, polyamines, amino acids and pyrridine carboxylic acids. Salts of these acids may also be used. The SO2 required may be obtained from part of the H2S absorbed in the solvent, e.g. by flashing off 35% of the H2S and oxidizing with air, or by oxidizing part of the sulphur produced in the process, or, at least partly, from SO2 which may be present in the gas to be treated. The gas is contacted in countercurrent with the solvent under a pressure of 70 atm. absolute, and treatment of the H2S-containing solvent is carried out at a pH between 0 and 8, and at a temperature between 26 DEG and 163 DEG C. This treatment may take place simultaneously with or subsequent to, the absorption. The solvent, after removal of sulphur and water equivalent to that formed in the reaction, is recycled.ALSO:Hydrogen sulphide in admixture with another gas, e.g. hydrogen and/or low boiling hydrocarbons, is absorbed in a solvent containing water, at least one sulphone, at least one ferrous salt and at least one chelating agent for ferrous ions, and the hydrogen sulphide-containing solvent is treated with SO2, whereby water and sulphur are formed. The water content of the solvent is preferably 2-20% by weight. The sulphone, at least 50% by weight, is preferably a hydrocarbyl sulphone, e.g. methyl ethyl, diethyl, di-n-propyl, dibenzyl or ditolyl sulphone, or tetrahydrothiophene-1, 1-dioxide or 2,3-dihydrothiophene - 1,1 - dioxide, or substitution derivatives of these containing not more than four alkyl groups per molecule, e.g. the 2,3-dimethyl, 2,4-dimethyl, 2,5-dimethyl, 3-ethyl or 2 - methyl - 5 - propyl derivatives of tetrahydrothiophene - 1,1 - dioxide. Hydroxyamino-or keto-sulphones may also be utilized. The ferrous salt, 0.5-10% by weight, may be ferrous nitrate, chloride or sulphate. The chelating agent, 0.1-5% by weight, or 0.1-1 molecule for each ferrous ion present, is any compound capable of forming one or more complexes with ferrous ions, the negative logarithm of the dissociation constant of the complexes being preferably in the range 0.2-10 in the temperature range -1 DEG to +150 DEG C., and suitable agents include alkyleneamine carboxylic acids, polyamines, amino acids and pyridine carboxylic acids. Salts of the acids may be used. The SO2 required may be obtained from part of the H2S absorbed in the solvent, e.g. by flashing off 35% of the H2S and oxidizing with air, or by oxidizing part of the sulphur produced in the process, or, at least partly, from SO2 which may be present in the gas to be treated. H2S is absorbed in countercurrent at 70 atm. abs., and treatment of the H2S-containing solvent is carried out at a pH between 0 and 8, and at a temperature between 26 DEG C. and 163 DEG C. This treatment may take place simultaneously with, or subsequent to, the absorption. The solvent, after removal of sulphur and water equivalent to that formed in the reaction, is recycled.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US19016062A | 1962-04-25 | 1962-04-25 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1005096A true GB1005096A (en) | 1965-09-22 |
Family
ID=22700251
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB1604963A Expired GB1005096A (en) | 1962-04-25 | 1963-04-23 | Process for the removal of hydrogen sulphide from gases |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB1005096A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4014983A (en) | 1975-04-07 | 1977-03-29 | Air Revources, Inc. | Removal of hydrogen sulfide from gases |
| US5273734A (en) * | 1990-01-12 | 1993-12-28 | The Texas A&M University System | Conversion of H2 to sulfur |
-
1963
- 1963-04-23 GB GB1604963A patent/GB1005096A/en not_active Expired
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4014983A (en) | 1975-04-07 | 1977-03-29 | Air Revources, Inc. | Removal of hydrogen sulfide from gases |
| US5273734A (en) * | 1990-01-12 | 1993-12-28 | The Texas A&M University System | Conversion of H2 to sulfur |
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