JP2016536115A5 - - Google Patents
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- JP2016536115A5 JP2016536115A5 JP2016524102A JP2016524102A JP2016536115A5 JP 2016536115 A5 JP2016536115 A5 JP 2016536115A5 JP 2016524102 A JP2016524102 A JP 2016524102A JP 2016524102 A JP2016524102 A JP 2016524102A JP 2016536115 A5 JP2016536115 A5 JP 2016536115A5
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- Prior art keywords
- amine
- diol
- gas
- mixtures
- group
- Prior art date
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- 239000000203 mixture Substances 0.000 claims description 69
- 150000001412 amines Chemical class 0.000 claims description 55
- 238000000034 method Methods 0.000 claims description 50
- 239000000243 solution Substances 0.000 claims description 43
- 239000002904 solvent Substances 0.000 claims description 33
- 239000002253 acid Substances 0.000 claims description 31
- 239000007864 aqueous solution Substances 0.000 claims description 16
- QCMHUGYTOGXZIW-UHFFFAOYSA-N 3-(dimethylamino)propane-1,2-diol Chemical compound CN(C)CC(O)CO QCMHUGYTOGXZIW-UHFFFAOYSA-N 0.000 claims description 14
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 13
- GLUUGHFHXGJENI-UHFFFAOYSA-N diethylenediamine Natural products C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 claims description 9
- 239000012190 activator Substances 0.000 claims description 8
- -1 hydroxymethyl-2-diethylaminopropane-1,3-diol Chemical compound 0.000 claims description 8
- LTACQVCHVAUOKN-UHFFFAOYSA-N 3-(diethylamino)propane-1,2-diol Chemical compound CCN(CC)CC(O)CO LTACQVCHVAUOKN-UHFFFAOYSA-N 0.000 claims description 7
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 claims description 7
- 125000001741 organic sulfur group Chemical group 0.000 claims description 7
- 239000002202 Polyethylene glycol Substances 0.000 claims description 5
- 229920001223 polyethylene glycol Polymers 0.000 claims description 5
- 150000003512 tertiary amines Chemical class 0.000 claims description 5
- PVOAHINGSUIXLS-UHFFFAOYSA-N 1-Methylpiperazine Chemical compound CN1CCNCC1 PVOAHINGSUIXLS-UHFFFAOYSA-N 0.000 claims description 4
- FGLZHYIVVZTBQJ-UHFFFAOYSA-N 2-(dimethylamino)-2-(hydroxymethyl)propane-1,3-diol Chemical compound CN(C)C(CO)(CO)CO FGLZHYIVVZTBQJ-UHFFFAOYSA-N 0.000 claims description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 4
- 229920001451 polypropylene glycol Polymers 0.000 claims description 4
- PCSHKVBVESYSBZ-UHFFFAOYSA-N 1-(2-hydroxypropylamino)propan-1-ol Chemical compound CCC(O)NCC(C)O PCSHKVBVESYSBZ-UHFFFAOYSA-N 0.000 claims description 3
- WFCSWCVEJLETKA-UHFFFAOYSA-N 2-piperazin-1-ylethanol Chemical compound OCCN1CCNCC1 WFCSWCVEJLETKA-UHFFFAOYSA-N 0.000 claims description 3
- CBTVGIZVANVGBH-UHFFFAOYSA-N aminomethyl propanol Chemical compound CC(C)(N)CO CBTVGIZVANVGBH-UHFFFAOYSA-N 0.000 claims description 3
- 238000009835 boiling Methods 0.000 claims description 3
- LXVCMYFHBTWKDO-UHFFFAOYSA-N 2-(diethylamino)-2-(hydroxymethyl)propane-1,3-diol Chemical compound CCN(CC)C(CO)(CO)CO LXVCMYFHBTWKDO-UHFFFAOYSA-N 0.000 claims description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 2
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 claims description 2
- 239000004327 boric acid Substances 0.000 claims description 2
- 150000005215 alkyl ethers Chemical class 0.000 claims 5
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 claims 3
- 150000001346 alkyl aryl ethers Chemical class 0.000 claims 3
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 claims 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 claims 2
- JOMNTHCQHJPVAZ-UHFFFAOYSA-N 2-methylpiperazine Chemical compound CC1CNCCN1 JOMNTHCQHJPVAZ-UHFFFAOYSA-N 0.000 claims 2
- OPKOKAMJFNKNAS-UHFFFAOYSA-N N-methylethanolamine Chemical compound CNCCO OPKOKAMJFNKNAS-UHFFFAOYSA-N 0.000 claims 2
- YZSDZIUZNIOTQR-UHFFFAOYSA-N 1-(methylamino)propane-1,3-diol Chemical compound CNC(O)CCO YZSDZIUZNIOTQR-UHFFFAOYSA-N 0.000 claims 1
- 125000004193 piperazinyl group Chemical group 0.000 claims 1
- 239000007789 gas Substances 0.000 description 79
- CRVGTESFCCXCTH-UHFFFAOYSA-N methyl diethanolamine Chemical compound OCCN(C)CCO CRVGTESFCCXCTH-UHFFFAOYSA-N 0.000 description 18
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 17
- 239000012530 fluid Substances 0.000 description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
- 238000004458 analytical method Methods 0.000 description 14
- 238000009472 formulation Methods 0.000 description 14
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 12
- 150000002898 organic sulfur compounds Chemical class 0.000 description 12
- 238000010521 absorption reaction Methods 0.000 description 11
- 239000003921 oil Substances 0.000 description 11
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 10
- 230000002378 acidificating effect Effects 0.000 description 10
- JJWKPURADFRFRB-UHFFFAOYSA-N carbonyl sulfide Chemical compound O=C=S JJWKPURADFRFRB-UHFFFAOYSA-N 0.000 description 10
- LELOWRISYMNNSU-UHFFFAOYSA-N hydrogen cyanide Chemical compound N#C LELOWRISYMNNSU-UHFFFAOYSA-N 0.000 description 10
- 239000007788 liquid Substances 0.000 description 10
- GODZNYBQGNSJJN-UHFFFAOYSA-N 1-aminoethane-1,2-diol Chemical compound NC(O)CO GODZNYBQGNSJJN-UHFFFAOYSA-N 0.000 description 8
- 239000006096 absorbing agent Substances 0.000 description 8
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 8
- 239000008246 gaseous mixture Substances 0.000 description 7
- 229910052739 hydrogen Inorganic materials 0.000 description 5
- 230000008929 regeneration Effects 0.000 description 5
- 238000011069 regeneration method Methods 0.000 description 5
- 229910052717 sulfur Inorganic materials 0.000 description 5
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 4
- 239000002250 absorbent Substances 0.000 description 4
- 230000002745 absorbent Effects 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- LVTYICIALWPMFW-UHFFFAOYSA-N diisopropanolamine Chemical compound CC(O)CNCC(C)O LVTYICIALWPMFW-UHFFFAOYSA-N 0.000 description 4
- 229940043276 diisopropanolamine Drugs 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 239000012535 impurity Substances 0.000 description 4
- 239000003112 inhibitor Substances 0.000 description 4
- 239000003345 natural gas Substances 0.000 description 4
- JLGLQAWTXXGVEM-UHFFFAOYSA-N triethylene glycol monomethyl ether Chemical compound COCCOCCOCCO JLGLQAWTXXGVEM-UHFFFAOYSA-N 0.000 description 4
- QGJOPFRUJISHPQ-UHFFFAOYSA-N Carbon disulfide Chemical compound S=C=S QGJOPFRUJISHPQ-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
- 239000002518 antifoaming agent Substances 0.000 description 3
- 238000003795 desorption Methods 0.000 description 3
- UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 description 3
- 239000011593 sulfur Substances 0.000 description 3
- GIAFURWZWWWBQT-UHFFFAOYSA-N 2-(2-aminoethoxy)ethanol Chemical compound NCCOCCO GIAFURWZWWWBQT-UHFFFAOYSA-N 0.000 description 2
- SBASXUCJHJRPEV-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethanol Chemical compound COCCOCCO SBASXUCJHJRPEV-UHFFFAOYSA-N 0.000 description 2
- KIHOFAGVAMNMHH-UHFFFAOYSA-N 2-(hydroxymethyl)-2-(methylamino)propane-1,3-diol Chemical compound CNC(CO)(CO)CO KIHOFAGVAMNMHH-UHFFFAOYSA-N 0.000 description 2
- LRDIEHDJWYRVPT-UHFFFAOYSA-N 4-amino-5-hydroxynaphthalene-1-sulfonic acid Chemical compound C1=CC(O)=C2C(N)=CC=C(S(O)(=O)=O)C2=C1 LRDIEHDJWYRVPT-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000001569 carbon dioxide Substances 0.000 description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003245 coal Substances 0.000 description 2
- 239000000356 contaminant Substances 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- 238000004817 gas chromatography Methods 0.000 description 2
- 150000002334 glycols Chemical class 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- 239000003915 liquefied petroleum gas Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 239000003079 shale oil Substances 0.000 description 2
- 241000894007 species Species 0.000 description 2
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- XXMBEHIWODXDTR-UHFFFAOYSA-N 1,2-diaminoethanol Chemical compound NCC(N)O XXMBEHIWODXDTR-UHFFFAOYSA-N 0.000 description 1
- IUQJDHJVPLLKFL-UHFFFAOYSA-N 2-(2,4-dichlorophenoxy)acetate;dimethylazanium Chemical compound CNC.OC(=O)COC1=CC=C(Cl)C=C1Cl IUQJDHJVPLLKFL-UHFFFAOYSA-N 0.000 description 1
- COBPKKZHLDDMTB-UHFFFAOYSA-N 2-[2-(2-butoxyethoxy)ethoxy]ethanol Chemical compound CCCCOCCOCCOCCO COBPKKZHLDDMTB-UHFFFAOYSA-N 0.000 description 1
- WFSMVVDJSNMRAR-UHFFFAOYSA-N 2-[2-(2-ethoxyethoxy)ethoxy]ethanol Chemical compound CCOCCOCCOCCO WFSMVVDJSNMRAR-UHFFFAOYSA-N 0.000 description 1
- 240000007124 Brassica oleracea Species 0.000 description 1
- 101710178035 Chorismate synthase 2 Proteins 0.000 description 1
- 101710152694 Cysteine synthase 2 Proteins 0.000 description 1
- DBAKFASWICGISY-DASCVMRKSA-N Dexchlorpheniramine maleate Chemical compound OC(=O)\C=C/C(O)=O.C1([C@H](CCN(C)C)C=2N=CC=CC=2)=CC=C(Cl)C=C1 DBAKFASWICGISY-DASCVMRKSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000000567 combustion gas Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- 229940043279 diisopropylamine Drugs 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- UESSEMPSSAXQJC-UHFFFAOYSA-N ethanol;methanamine Chemical compound NC.CCO UESSEMPSSAXQJC-UHFFFAOYSA-N 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000000295 fuel oil Substances 0.000 description 1
- 238000002309 gasification Methods 0.000 description 1
- 231100001261 hazardous Toxicity 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000010742 number 1 fuel oil Substances 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 150000004885 piperazines Chemical class 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 238000011403 purification operation Methods 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003464 sulfur compounds Chemical class 0.000 description 1
- 239000012808 vapor phase Substances 0.000 description 1
Images
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361897687P | 2013-10-30 | 2013-10-30 | |
| US61/897,687 | 2013-10-30 | ||
| PCT/US2014/062163 WO2015065842A1 (en) | 2013-10-30 | 2014-10-24 | Hybrid solvent formulations for total organic sulfur removal and total acidic gas removal |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2016536115A JP2016536115A (ja) | 2016-11-24 |
| JP2016536115A5 true JP2016536115A5 (enExample) | 2017-11-24 |
Family
ID=51869048
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016524102A Pending JP2016536115A (ja) | 2013-10-30 | 2014-10-24 | 全有機硫黄除去及び全酸性ガス除去のための混成溶媒配合物 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US10293299B2 (enExample) |
| EP (1) | EP3062912A1 (enExample) |
| JP (1) | JP2016536115A (enExample) |
| CN (1) | CN105658306A (enExample) |
| CA (1) | CA2927937A1 (enExample) |
| EA (1) | EA201690897A1 (enExample) |
| MX (1) | MX2016004837A (enExample) |
| WO (1) | WO2015065842A1 (enExample) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MX2016004836A (es) | 2013-10-30 | 2016-07-26 | Dow Global Technologies Llc | Formulaciones solventes hibridas para la remocion selectiva de sulfuro de hidrogeno (h2s). |
| EA201690897A1 (ru) | 2013-10-30 | 2016-12-30 | ДАУ ГЛОБАЛ ТЕКНОЛОДЖИЗ ЭлЭлСи | Композиции гибридных растворителей для полного удаления органической серы и полного удаления кислого газа |
| EP3204142A1 (en) * | 2014-10-10 | 2017-08-16 | Dow Global Technologies LLC | Aqueous solution of 2-dimethylamino-2-hydroxymethyl-1, 3-propanediol useful for acid gas removal from gaseous mixtures |
| CN106479586A (zh) * | 2016-12-05 | 2017-03-08 | 江苏汉光实业股份有限公司 | 环保型h2s脱除剂及其制备方法 |
| CN107464669A (zh) * | 2017-09-26 | 2017-12-12 | 绵阳鑫阳知识产权运营有限公司 | 可延长变压器油使用寿命的油枕气管 |
| CA3090928A1 (en) | 2018-02-14 | 2019-08-22 | Taminco Bvba | Improved contaminant removal process |
| WO2020106396A1 (en) * | 2018-11-19 | 2020-05-28 | Exxonmobil Upstream Research Company | Co-current gas absortion method and system with an enhanced absorbent |
| US11090604B2 (en) | 2018-11-19 | 2021-08-17 | Exxonmobil Upstream Research Company | Enhanced acid gas removal within a gas processing system |
| CN113710644A (zh) * | 2019-04-16 | 2021-11-26 | 安格斯化学公司 | 低毒性有机叔胺和季胺及其用途 |
| CN116262190B (zh) * | 2021-12-13 | 2024-10-01 | 中国石油天然气股份有限公司 | 一种高适应性有机硫脱除溶剂及有机硫脱除方法 |
| CN114699882B (zh) * | 2022-03-11 | 2024-06-14 | 华东理工大学 | 高效吸收脱除有机硫化合物的醚胺类化合物及其设计方法和应用 |
| WO2024180358A1 (en) * | 2023-02-27 | 2024-09-06 | Totalenergies Onetech | Method for selective separation of hydrogen sulfide from a gas mixture |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4044100A (en) * | 1969-12-08 | 1977-08-23 | Allied Chemical Corporation | Separation of acidic gas constituents from gaseous mixtures containing the same |
| US4085192A (en) | 1973-05-11 | 1978-04-18 | Shell Oil Company | Selective removal of hydrogen sulfide from gaseous mixtures |
| DE2551717C3 (de) | 1975-11-18 | 1980-11-13 | Basf Ag, 6700 Ludwigshafen | und ggf. COS aus Gasen |
| SU927282A1 (ru) * | 1979-04-25 | 1982-05-15 | Всесоюзный Научно-Исследовательский И Проектный Институт По Подготовке @К Транспортировке И Переработке Природного Газа | Абсорбент дл очистки газов от кислых компонентов |
| IT1132170B (it) | 1980-07-04 | 1986-06-25 | Snam Progetti | Processo di separazione selettiva di idrogeno solforato da miscele gassose contenenti anche anidride carbonica |
| US4405585A (en) | 1982-01-18 | 1983-09-20 | Exxon Research And Engineering Co. | Process for the selective removal of hydrogen sulfide from gaseous mixtures with severely sterically hindered secondary aminoether alcohols |
| JPS6048116A (ja) * | 1983-06-30 | 1985-03-15 | ユニオン、カ−バイド、コ−ポレ−シヨン | ガス混合物から酸性ガスを増大除去するための吸収剤組成物及びそれを使用する方法 |
| EP0134948A3 (en) | 1983-06-30 | 1987-10-14 | Union Carbide Corporation | Absorbent formulation for enhanced removal of acid gases from gas mixtures and processes using same |
| US4484934A (en) * | 1984-01-27 | 1984-11-27 | Combustion Engineering, Inc. | Physical solvent for gas sweetening |
| DE3408851A1 (de) | 1984-03-10 | 1985-09-12 | Basf Ag, 6700 Ludwigshafen | Verfahren zum entfernen von co(pfeil abwaerts)2(pfeil abwaerts) und/oder h(pfeil abwaerts)2(pfeil abwaerts)s aus gasen |
| US4705673A (en) * | 1984-10-10 | 1987-11-10 | Union Carbide Corporation | Mixed solvent system for treating acidic gas |
| WO1986005474A1 (en) | 1985-03-14 | 1986-09-25 | The Ralph M. Parsons Company | Selective absorption of hydrogene sulfide from gases which also contain carbon dioxide |
| US4892674A (en) | 1987-10-13 | 1990-01-09 | Exxon Research And Engineering Company | Addition of severely-hindered amine salts and/or aminoacids to non-hindered amine solutions for the absorption of H2 S |
| EP0728033B1 (en) | 1993-11-09 | 1999-04-21 | Union Carbide Chemicals & Plastics Technology Corporation | Absorption of mercaptans |
| JP3392609B2 (ja) | 1995-12-01 | 2003-03-31 | 三菱重工業株式会社 | ガス中の炭酸ガスを除去する方法 |
| JP3198077B2 (ja) | 1997-06-27 | 2001-08-13 | 住友ゴム工業株式会社 | 空気入りタイヤ |
| DE19828977A1 (de) * | 1998-06-29 | 1999-12-30 | Basf Ag | Verfahren zur Entfernung saurer Gasbestandteile aus Gasen |
| US6337059B1 (en) | 1999-05-03 | 2002-01-08 | Union Carbide Chemicals & Plastics Technology Corporation | Absorbent compositions for the removal of acid gases from gas streams |
| US7144555B1 (en) * | 2001-06-20 | 2006-12-05 | Well To Wire Emissions Control Inc. | Method and apparatus for hydrogen sulphide removal |
| EP1718597B1 (en) | 2004-02-17 | 2016-09-07 | ExxonMobil Research and Engineering Company | Improved synthesis of severely sterically hindered amino-ether alcohols and diaminopolyalkenyl ethers using a high activity powder catalyst |
| JP5612583B2 (ja) * | 2008-10-06 | 2014-10-22 | ダウ グローバル テクノロジーズ エルエルシー | エチレンオキサイド及びアンモニアからのエタノールアミン及びエチレンアミンの製造方法並びに関連方法 |
| US8221712B2 (en) | 2009-05-12 | 2012-07-17 | Basf Se | Absorption medium for the selective removal of hydrogen sulfide from fluid streams |
| EP2283911A1 (en) * | 2009-08-11 | 2011-02-16 | Shell Internationale Research Maatschappij B.V. | Process for removing CO2 and/or H2S from a gas comprising CO2 and/or H2S |
| CA2769617A1 (en) | 2009-08-11 | 2011-02-17 | Shell Internationale Research Maatschappij B.V. | Absorbent composition and process for removing co2 and/or h2s from a gas comprising co2 and/or h2s |
| KR101181584B1 (ko) * | 2010-09-28 | 2012-09-10 | 순천향대학교 산학협력단 | 침적 슬러지의 물리화학적 세정방법 |
| FR2982170B1 (fr) | 2011-11-09 | 2013-11-22 | IFP Energies Nouvelles | Procede d'elimination de composes acides d'un effluent gazeux avec une solution absorbante a base de dihydroxyalkylamines possedant un encombrement sterique severe de l'atome d'azote |
| RU2642071C2 (ru) * | 2012-06-29 | 2018-01-24 | ДАУ ГЛОБАЛ ТЕКНОЛОДЖИЗ ЭлЭлСи | Водная алканоламиновая абсорбирующая композиция, содержащая пиперазин для улучшенного удаления сероводорода из газовых смесей, и способ ее использования |
| JP6290878B2 (ja) * | 2012-06-29 | 2018-03-07 | ダウ グローバル テクノロジーズ エルエルシー | ガス混合物からｈ２ｓを除去する、水性アルカノールアミン溶液及び工程 |
| EA201690897A1 (ru) | 2013-10-30 | 2016-12-30 | ДАУ ГЛОБАЛ ТЕКНОЛОДЖИЗ ЭлЭлСи | Композиции гибридных растворителей для полного удаления органической серы и полного удаления кислого газа |
| MX2016004836A (es) | 2013-10-30 | 2016-07-26 | Dow Global Technologies Llc | Formulaciones solventes hibridas para la remocion selectiva de sulfuro de hidrogeno (h2s). |
-
2014
- 2014-10-24 EA EA201690897A patent/EA201690897A1/ru unknown
- 2014-10-24 US US15/032,868 patent/US10293299B2/en active Active
- 2014-10-24 MX MX2016004837A patent/MX2016004837A/es unknown
- 2014-10-24 JP JP2016524102A patent/JP2016536115A/ja active Pending
- 2014-10-24 WO PCT/US2014/062163 patent/WO2015065842A1/en not_active Ceased
- 2014-10-24 CA CA2927937A patent/CA2927937A1/en not_active Abandoned
- 2014-10-24 CN CN201480057375.XA patent/CN105658306A/zh active Pending
- 2014-10-24 EP EP14795917.5A patent/EP3062912A1/en not_active Withdrawn
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