NO316938B1 - Fremgangsmate og anordning for behandling av en gass inneholdende hydrogensulfid, med resirkulering av den reduserte katalytiske opplosning - Google Patents
Fremgangsmate og anordning for behandling av en gass inneholdende hydrogensulfid, med resirkulering av den reduserte katalytiske opplosning Download PDFInfo
- Publication number
- NO316938B1 NO316938B1 NO20002975A NO20002975A NO316938B1 NO 316938 B1 NO316938 B1 NO 316938B1 NO 20002975 A NO20002975 A NO 20002975A NO 20002975 A NO20002975 A NO 20002975A NO 316938 B1 NO316938 B1 NO 316938B1
- Authority
- NO
- Norway
- Prior art keywords
- sulfur
- catalytic solution
- solution
- fraction
- reduced
- Prior art date
Links
- 230000003197 catalytic effect Effects 0.000 title claims description 79
- 238000000034 method Methods 0.000 title claims description 49
- 230000002829 reductive effect Effects 0.000 title claims description 48
- 239000007789 gas Substances 0.000 title claims description 40
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 title claims description 27
- 238000004064 recycling Methods 0.000 title claims description 11
- 229910000037 hydrogen sulfide Inorganic materials 0.000 title claims description 8
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 119
- 229910052717 sulfur Inorganic materials 0.000 claims description 99
- 239000011593 sulfur Substances 0.000 claims description 99
- 238000010521 absorption reaction Methods 0.000 claims description 45
- 238000000926 separation method Methods 0.000 claims description 24
- 230000008929 regeneration Effects 0.000 claims description 19
- 238000011069 regeneration method Methods 0.000 claims description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 19
- 230000008569 process Effects 0.000 claims description 18
- 238000001914 filtration Methods 0.000 claims description 17
- 229910052751 metal Inorganic materials 0.000 claims description 16
- 239000002184 metal Substances 0.000 claims description 16
- 230000003647 oxidation Effects 0.000 claims description 14
- 238000007254 oxidation reaction Methods 0.000 claims description 14
- 239000002245 particle Substances 0.000 claims description 12
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 10
- 238000001728 nano-filtration Methods 0.000 claims description 10
- 238000001223 reverse osmosis Methods 0.000 claims description 10
- 239000007787 solid Substances 0.000 claims description 9
- VTLYFUHAOXGGBS-UHFFFAOYSA-N Fe3+ Chemical compound [Fe+3] VTLYFUHAOXGGBS-UHFFFAOYSA-N 0.000 claims description 8
- 239000002738 chelating agent Substances 0.000 claims description 7
- 229910001447 ferric ion Inorganic materials 0.000 claims description 7
- 238000009826 distribution Methods 0.000 claims description 6
- 150000002500 ions Chemical class 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 5
- 230000009467 reduction Effects 0.000 claims description 5
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 4
- 230000001590 oxidative effect Effects 0.000 claims description 4
- 229910052760 oxygen Inorganic materials 0.000 claims description 4
- 239000001301 oxygen Substances 0.000 claims description 4
- 239000003345 natural gas Substances 0.000 claims description 3
- 238000005194 fractionation Methods 0.000 claims description 2
- 239000000126 substance Substances 0.000 claims description 2
- 230000001276 controlling effect Effects 0.000 claims 1
- 239000000463 material Substances 0.000 claims 1
- 230000001105 regulatory effect Effects 0.000 claims 1
- 239000000243 solution Substances 0.000 description 119
- 239000003054 catalyst Substances 0.000 description 22
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 11
- 238000006555 catalytic reaction Methods 0.000 description 11
- 238000005406 washing Methods 0.000 description 6
- 239000005864 Sulphur Substances 0.000 description 5
- 229910052742 iron Inorganic materials 0.000 description 5
- YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 238000004140 cleaning Methods 0.000 description 3
- 238000011010 flushing procedure Methods 0.000 description 3
- 239000012528 membrane Substances 0.000 description 3
- MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 3
- 238000006479 redox reaction Methods 0.000 description 3
- 238000006722 reduction reaction Methods 0.000 description 3
- 238000007086 side reaction Methods 0.000 description 3
- ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 230000002776 aggregation Effects 0.000 description 2
- 235000011130 ammonium sulphate Nutrition 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- PYRZPBDTPRQYKG-UHFFFAOYSA-N cyclopentene-1-carboxylic acid Chemical compound OC(=O)C1=CCCC1 PYRZPBDTPRQYKG-UHFFFAOYSA-N 0.000 description 2
- 238000010908 decantation Methods 0.000 description 2
- 238000007872 degassing Methods 0.000 description 2
- 238000006477 desulfuration reaction Methods 0.000 description 2
- 230000023556 desulfurization Effects 0.000 description 2
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 2
- 230000008030 elimination Effects 0.000 description 2
- 238000003379 elimination reaction Methods 0.000 description 2
- 238000005187 foaming Methods 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- LCEDQNDDFOCWGG-UHFFFAOYSA-N morpholine-4-carbaldehyde Chemical compound O=CN1CCOCC1 LCEDQNDDFOCWGG-UHFFFAOYSA-N 0.000 description 2
- 239000007800 oxidant agent Substances 0.000 description 2
- 230000033116 oxidation-reduction process Effects 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- AVFZOVWCLRSYKC-UHFFFAOYSA-N 1-methylpyrrolidine Chemical compound CN1CCCC1 AVFZOVWCLRSYKC-UHFFFAOYSA-N 0.000 description 1
- WYMDDFRYORANCC-UHFFFAOYSA-N 2-[[3-[bis(carboxymethyl)amino]-2-hydroxypropyl]-(carboxymethyl)amino]acetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)CN(CC(O)=O)CC(O)=O WYMDDFRYORANCC-UHFFFAOYSA-N 0.000 description 1
- WXHLLJAMBQLULT-UHFFFAOYSA-N 2-[[6-[4-(2-hydroxyethyl)piperazin-1-yl]-2-methylpyrimidin-4-yl]amino]-n-(2-methyl-6-sulfanylphenyl)-1,3-thiazole-5-carboxamide;hydrate Chemical compound O.C=1C(N2CCN(CCO)CC2)=NC(C)=NC=1NC(S1)=NC=C1C(=O)NC1=C(C)C=CC=C1S WXHLLJAMBQLULT-UHFFFAOYSA-N 0.000 description 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- ZEYKLMDPUOVUCR-UHFFFAOYSA-N 2-chloro-5-(trifluoromethyl)benzenesulfonyl chloride Chemical compound FC(F)(F)C1=CC=C(Cl)C(S(Cl)(=O)=O)=C1 ZEYKLMDPUOVUCR-UHFFFAOYSA-N 0.000 description 1
- 125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 description 1
- MEUAVGJWGDPTLF-UHFFFAOYSA-N 4-(5-benzenesulfonylamino-1-methyl-1h-benzoimidazol-2-ylmethyl)-benzamidine Chemical compound N=1C2=CC(NS(=O)(=O)C=3C=CC=CC=3)=CC=C2N(C)C=1CC1=CC=C(C(N)=N)C=C1 MEUAVGJWGDPTLF-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- QPCDCPDFJACHGM-UHFFFAOYSA-N N,N-bis{2-[bis(carboxymethyl)amino]ethyl}glycine Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(=O)O)CCN(CC(O)=O)CC(O)=O QPCDCPDFJACHGM-UHFFFAOYSA-N 0.000 description 1
- AHVYPIQETPWLSZ-UHFFFAOYSA-N N-methyl-pyrrolidine Natural products CN1CC=CC1 AHVYPIQETPWLSZ-UHFFFAOYSA-N 0.000 description 1
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 239000001166 ammonium sulphate Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 230000000536 complexating effect Effects 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- IRXRGVFLQOSHOH-UHFFFAOYSA-L dipotassium;oxalate Chemical compound [K+].[K+].[O-]C(=O)C([O-])=O IRXRGVFLQOSHOH-UHFFFAOYSA-L 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229910001448 ferrous ion Inorganic materials 0.000 description 1
- 238000005188 flotation Methods 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000010297 mechanical methods and process Methods 0.000 description 1
- 230000005226 mechanical processes and functions Effects 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 150000002898 organic sulfur compounds Chemical class 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 230000036961 partial effect Effects 0.000 description 1
- 229960003330 pentetic acid Drugs 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- OTYBMLCTZGSZBG-UHFFFAOYSA-L potassium sulfate Chemical class [K+].[K+].[O-]S([O-])(=O)=O OTYBMLCTZGSZBG-UHFFFAOYSA-L 0.000 description 1
- 239000001120 potassium sulphate Substances 0.000 description 1
- 235000011151 potassium sulphates Nutrition 0.000 description 1
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 230000001172 regenerating effect Effects 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
- 150000003463 sulfur Chemical class 0.000 description 1
- 238000005987 sulfurization reaction Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- DHCDFWKWKRSZHF-UHFFFAOYSA-L thiosulfate(2-) Chemical compound [O-]S([S-])(=O)=O DHCDFWKWKRSZHF-UHFFFAOYSA-L 0.000 description 1
- 238000002604 ultrasonography Methods 0.000 description 1
- 238000011144 upstream manufacturing Methods 0.000 description 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
- B01D53/14—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
- B01D53/1468—Removing hydrogen sulfide
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Analytical Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Gas Separation By Absorption (AREA)
- Catalysts (AREA)
- Treating Waste Gases (AREA)
- Separation Using Semi-Permeable Membranes (AREA)
- Degasification And Air Bubble Elimination (AREA)
- Exhaust Gas Treatment By Means Of Catalyst (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9907359A FR2794664B1 (fr) | 1999-06-10 | 1999-06-10 | Procede et dispositif de traitement d'un gaz contenant de l'hydrogene sulfure, avec recyclage de la solution catalytique reduite |
Publications (3)
Publication Number | Publication Date |
---|---|
NO20002975D0 NO20002975D0 (no) | 2000-06-09 |
NO20002975L NO20002975L (no) | 2000-12-11 |
NO316938B1 true NO316938B1 (no) | 2004-06-28 |
Family
ID=9546635
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO20002975A NO316938B1 (no) | 1999-06-10 | 2000-06-09 | Fremgangsmate og anordning for behandling av en gass inneholdende hydrogensulfid, med resirkulering av den reduserte katalytiske opplosning |
Country Status (9)
Country | Link |
---|---|
US (1) | US6589498B1 (de) |
EP (1) | EP1059111B1 (de) |
JP (1) | JP4520585B2 (de) |
AR (1) | AR024322A1 (de) |
CA (1) | CA2311276C (de) |
DE (1) | DE60033086T2 (de) |
ES (1) | ES2280181T3 (de) |
FR (1) | FR2794664B1 (de) |
NO (1) | NO316938B1 (de) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100825328B1 (ko) * | 2001-11-27 | 2008-04-28 | 주식회사 포스코 | 탈황설비 반응로 내부 유출촉매 분리 및 회수장치 |
DE60303364T2 (de) * | 2002-04-08 | 2006-09-07 | Akzo Nobel N.V. | Verfahren zur entfernung eines stickoxides aus einem mit diesem beladenen gas |
US7226883B1 (en) * | 2006-06-05 | 2007-06-05 | Merichem Chemicals & Refinery Services Llc | Oxidizer and oxidation process for a desulphurization process |
TWI454304B (zh) * | 2012-10-08 | 2014-10-01 | Univ Nat Chiao Tung | 高濃度硫化氫去除系統及方法 |
MX2019004521A (es) * | 2016-10-14 | 2019-11-28 | Biosystems Consulting Inc Dba Advanced Oxidation Tech | Tratamiento del gas de sulfuro de hidrógeno en condiciones aeróbicas. |
CN108686489B (zh) * | 2017-04-12 | 2021-01-01 | 北京华石联合能源科技发展有限公司 | 一种悬浮床湿法脱硫工艺 |
CN108722161A (zh) * | 2018-08-16 | 2018-11-02 | 盘锦道博尔环保科技股份有限公司 | 一种脱除油田伴、次生气中硫化氢的系统及方法 |
CN111330438A (zh) * | 2020-03-25 | 2020-06-26 | 韩建英 | 一种工业烟气催化氧化脱硫方法 |
Family Cites Families (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5331587A (en) * | 1976-09-07 | 1978-03-24 | Mitsui Eng & Shipbuild Co Ltd | Simultaneous removing method for sulfur dioxide and hydrogen sulfide in exhaust gas |
JPS5689820A (en) * | 1979-12-21 | 1981-07-21 | Tokyo Gas Co Ltd | Removing method of hydrogen sulfide |
JPS582207A (ja) * | 1981-05-26 | 1983-01-07 | シエル・インタ−ナシヨネイル・リサ−チ・マ−チヤツピイ・ベ−・ウイ | 硫黄回収方法 |
DE3444252A1 (de) * | 1983-12-12 | 1985-06-20 | Chemengineering Co. Ltd., Zug | Verfahren und vorrichtung zur entfernung von schwefelwasserstoffen aus gasen |
US4532118A (en) * | 1984-03-29 | 1985-07-30 | Kimura Chemical Plants Co., Ltd. | Process for removal of hydrogen sulfide from gases |
JPS61216737A (ja) * | 1985-03-22 | 1986-09-26 | Kawasaki Kasei Chem Ltd | 硫化物の湿式酸化用レドックス触媒及び湿式酸化方法 |
IN168471B (de) * | 1985-08-23 | 1991-04-13 | Shell Int Research | |
US4859436A (en) * | 1985-08-23 | 1989-08-22 | Shell Oil Company | H2 S removal process and composition |
US4808385A (en) * | 1986-03-10 | 1989-02-28 | The Dow Chemical Company | Process for the removal of H2 S from fluid streams using a water soluble polymeric chelate of an oxidizing polyvalent metal |
AU594547B2 (en) * | 1986-12-30 | 1990-03-08 | Shell Internationale Research Maatschappij B.V. | Hydrogen sulfide removal from gas streams |
US4784775A (en) * | 1987-03-02 | 1988-11-15 | Ari Technologies, Inc. | Removal of hydrogen sulfide from sour water |
GB9017373D0 (en) * | 1990-08-08 | 1990-09-19 | Shell Int Research | Removing h2s from a sour gaseous stream |
BR9205847A (pt) * | 1991-03-28 | 1994-08-02 | Dow Chemical Co | Processo para a remoção de sulfeto de hidrogênio de um fluxo gasoso e aparelho para purificar uma solução aquosa de reação |
US5753189A (en) * | 1995-05-19 | 1998-05-19 | Gas Research Institute | Method and apparatus for controlling sulfur concentration in liquid redox sulfur removal processes |
-
1999
- 1999-06-10 FR FR9907359A patent/FR2794664B1/fr not_active Expired - Lifetime
-
2000
- 2000-05-24 EP EP00401450A patent/EP1059111B1/de not_active Expired - Lifetime
- 2000-05-24 DE DE60033086T patent/DE60033086T2/de not_active Expired - Lifetime
- 2000-05-24 ES ES00401450T patent/ES2280181T3/es not_active Expired - Lifetime
- 2000-06-07 AR ARP000102848A patent/AR024322A1/es active IP Right Grant
- 2000-06-08 CA CA2311276A patent/CA2311276C/fr not_active Expired - Lifetime
- 2000-06-09 NO NO20002975A patent/NO316938B1/no not_active IP Right Cessation
- 2000-06-09 US US09/589,744 patent/US6589498B1/en not_active Expired - Lifetime
- 2000-06-12 JP JP2000175209A patent/JP4520585B2/ja not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
NO20002975D0 (no) | 2000-06-09 |
DE60033086D1 (de) | 2007-03-15 |
DE60033086T2 (de) | 2007-05-10 |
CA2311276A1 (fr) | 2000-12-10 |
FR2794664B1 (fr) | 2001-07-13 |
US6589498B1 (en) | 2003-07-08 |
FR2794664A1 (fr) | 2000-12-15 |
CA2311276C (fr) | 2010-08-10 |
NO20002975L (no) | 2000-12-11 |
AR024322A1 (es) | 2002-09-25 |
EP1059111A1 (de) | 2000-12-13 |
JP2001025640A (ja) | 2001-01-30 |
ES2280181T3 (es) | 2007-09-16 |
JP4520585B2 (ja) | 2010-08-04 |
EP1059111B1 (de) | 2007-01-24 |
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