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GB1005096A - Process for the removal of hydrogen sulphide from gases - Google Patents

Process for the removal of hydrogen sulphide from gases

Info

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
Application number
GB1604963A
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.)
SHELL INT RESEARCH
Shell Internationale Research Maatschappij BV
Original Assignee
SHELL INT RESEARCH
Shell Internationale Research Maatschappij BV
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 SHELL INT RESEARCH, Shell Internationale Research Maatschappij BV filed Critical SHELL INT RESEARCH
Publication of GB1005096A publication Critical patent/GB1005096A/en
Expired legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation 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
    • B01D53/34Chemical or biological purification of waste gases
    • B01D53/46Removing components of defined structure
    • B01D53/48Sulfur compounds
    • B01D53/52Hydrogen sulfide
    • B01D53/523Mixtures 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.
GB1604963A 1962-04-25 1963-04-23 Process for the removal of hydrogen sulphide from gases Expired GB1005096A (en)

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)

* Cited by examiner, † Cited by third party
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

Cited By (2)

* Cited by examiner, † Cited by third party
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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