RU2614955C2 - Низкотемпературная транспортировка и хранение аминоэфирных растворов для обработки газа - Google Patents
Низкотемпературная транспортировка и хранение аминоэфирных растворов для обработки газа Download PDFInfo
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- RU2614955C2 RU2614955C2 RU2014139220A RU2014139220A RU2614955C2 RU 2614955 C2 RU2614955 C2 RU 2614955C2 RU 2014139220 A RU2014139220 A RU 2014139220A RU 2014139220 A RU2014139220 A RU 2014139220A RU 2614955 C2 RU2614955 C2 RU 2614955C2
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- RU
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- Prior art keywords
- amino
- tert
- mixture
- water
- amino ester
- Prior art date
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- 238000003860 storage Methods 0.000 title claims description 8
- 239000000203 mixture Substances 0.000 claims abstract description 38
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 38
- 238000007710 freezing Methods 0.000 claims abstract description 27
- 230000008014 freezing Effects 0.000 claims abstract description 27
- 239000002253 acid Substances 0.000 claims abstract description 20
- 239000002250 absorbent Substances 0.000 claims abstract description 17
- 230000002745 absorbent Effects 0.000 claims abstract description 17
- 239000007788 liquid Substances 0.000 claims abstract description 13
- 238000002156 mixing Methods 0.000 claims abstract description 5
- -1 amino ester Chemical class 0.000 claims description 64
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 25
- 238000000034 method Methods 0.000 claims description 21
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 11
- SBOJXQVPLKSXOG-UHFFFAOYSA-N o-amino-hydroxylamine Chemical compound NON SBOJXQVPLKSXOG-UHFFFAOYSA-N 0.000 claims description 10
- 230000002378 acidificating effect Effects 0.000 claims description 6
- 125000003277 amino group Chemical group 0.000 claims description 5
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims description 5
- HLAOLWFKQBAKSM-UHFFFAOYSA-N n-[2-[1-[2-(tert-butylamino)ethoxy]ethoxy]ethyl]-2-methylpropan-2-amine Chemical compound CC(C)(C)NCCOC(C)OCCNC(C)(C)C HLAOLWFKQBAKSM-UHFFFAOYSA-N 0.000 claims description 5
- OGXACZGMMBJZJA-UHFFFAOYSA-N CC(C)(C)N.CCOCCOC(C)O Chemical compound CC(C)(C)N.CCOCCOC(C)O OGXACZGMMBJZJA-UHFFFAOYSA-N 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 3
- 229920001223 polyethylene glycol Polymers 0.000 claims description 2
- 239000002202 Polyethylene glycol Substances 0.000 claims 1
- 125000006318 tert-butyl amino group Chemical group [H]N(*)C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- 239000000126 substance Substances 0.000 abstract description 12
- 230000000694 effects Effects 0.000 abstract 1
- 239000007789 gas Substances 0.000 description 37
- 150000001412 amines Chemical class 0.000 description 25
- UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 description 12
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 12
- 125000000217 alkyl group Chemical group 0.000 description 10
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 10
- 238000004834 15N NMR spectroscopy Methods 0.000 description 8
- 150000002148 esters Chemical class 0.000 description 8
- 239000007864 aqueous solution Substances 0.000 description 7
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 7
- 238000010521 absorption reaction Methods 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 6
- CRVGTESFCCXCTH-UHFFFAOYSA-N methyl diethanolamine Chemical compound OCCN(C)CCO CRVGTESFCCXCTH-UHFFFAOYSA-N 0.000 description 6
- 239000002594 sorbent Substances 0.000 description 6
- YBRBMKDOPFTVDT-UHFFFAOYSA-N tert-butylamine Chemical compound CC(C)(C)N YBRBMKDOPFTVDT-UHFFFAOYSA-N 0.000 description 6
- 229910052757 nitrogen Inorganic materials 0.000 description 5
- 125000004433 nitrogen atom Chemical group N* 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 238000003786 synthesis reaction Methods 0.000 description 5
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 230000003197 catalytic effect Effects 0.000 description 4
- 229940043279 diisopropylamine Drugs 0.000 description 4
- 239000012530 fluid Substances 0.000 description 4
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 4
- 229910052717 sulfur Inorganic materials 0.000 description 4
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 3
- BFSVOASYOCHEOV-UHFFFAOYSA-N 2-diethylaminoethanol Chemical compound CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 150000001721 carbon Chemical group 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- JLGLQAWTXXGVEM-UHFFFAOYSA-N triethylene glycol monomethyl ether Chemical compound COCCOCCOCCO JLGLQAWTXXGVEM-UHFFFAOYSA-N 0.000 description 3
- AGZLRXFVPQINSB-UHFFFAOYSA-N 1-[(tert-butylamino)methoxy]-1-(2-ethoxyethoxy)ethanol Chemical compound C(C)(C)(C)NCOC(C)(O)OCCOCC AGZLRXFVPQINSB-UHFFFAOYSA-N 0.000 description 2
- AHXXIYFEJGGBMG-UHFFFAOYSA-N 1-[2-(tert-butylamino)ethoxy]ethanol Chemical compound CC(O)OCCNC(C)(C)C AHXXIYFEJGGBMG-UHFFFAOYSA-N 0.000 description 2
- IEFVEOWKRKQABF-UHFFFAOYSA-N 1-[2-[2-(tert-butylamino)ethoxy]ethoxy]ethanol Chemical compound C(C)(C)(C)NCCOCCOC(C)O IEFVEOWKRKQABF-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 240000007124 Brassica oleracea Species 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- 125000000033 alkoxyamino group Chemical group 0.000 description 2
- 150000001414 amino alcohols Chemical group 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000003245 coal Substances 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 239000003345 natural gas Substances 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 150000003141 primary amines Chemical class 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 238000007711 solidification Methods 0.000 description 2
- 230000008023 solidification Effects 0.000 description 2
- 150000003463 sulfur Chemical class 0.000 description 2
- YUFFSWGQGVEMMI-JLNKQSITSA-N (7Z,10Z,13Z,16Z,19Z)-docosapentaenoic acid Chemical compound CC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CCCCCC(O)=O YUFFSWGQGVEMMI-JLNKQSITSA-N 0.000 description 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 1
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 description 1
- AVHVLGPVDJFOFA-UHFFFAOYSA-N 1,1-bis(tert-butylamino)-2-[2-(2-hydroxyethoxy)ethoxy]ethanol Chemical compound CC(C)(C)NC(O)(NC(C)(C)C)COCCOCCO AVHVLGPVDJFOFA-UHFFFAOYSA-N 0.000 description 1
- AGYUOJIYYGGHKV-UHFFFAOYSA-N 1,2-bis(2-chloroethoxy)ethane Chemical compound ClCCOCCOCCCl AGYUOJIYYGGHKV-UHFFFAOYSA-N 0.000 description 1
- QVWRZQHTUYIGTR-UHFFFAOYSA-N 1-(2-chloroethoxy)-1-ethoxyethanol Chemical compound CCOC(C)(O)OCCCl QVWRZQHTUYIGTR-UHFFFAOYSA-N 0.000 description 1
- VIQMARVUUSSXFD-UHFFFAOYSA-N 1-[2-(2-methoxyethoxy)ethoxy]ethanol 2-methylpropan-2-amine Chemical compound C(C)(C)(C)N.COCCOCCOC(C)O VIQMARVUUSSXFD-UHFFFAOYSA-N 0.000 description 1
- CFVWWFIAONUICG-UHFFFAOYSA-N 1-[2-(butan-2-ylamino)ethoxy]ethanol Chemical compound C(C)(CC)NCCOC(C)O CFVWWFIAONUICG-UHFFFAOYSA-N 0.000 description 1
- SJOPWQBFFNVXQB-UHFFFAOYSA-N 1-[2-(butylamino)ethoxy]ethanol Chemical compound CCCCNCCOC(C)O SJOPWQBFFNVXQB-UHFFFAOYSA-N 0.000 description 1
- VJRXEJXVFJDYJH-UHFFFAOYSA-N 1-ethoxyethanol;2-methylpropan-2-amine Chemical compound CC(C)(C)N.CCOC(C)O VJRXEJXVFJDYJH-UHFFFAOYSA-N 0.000 description 1
- GIAFURWZWWWBQT-UHFFFAOYSA-N 2-(2-aminoethoxy)ethanol Chemical compound NCCOCCO GIAFURWZWWWBQT-UHFFFAOYSA-N 0.000 description 1
- YSVQAQXTVLLNBA-UHFFFAOYSA-N 2-[2-(2-hydroxyethoxy)ethoxy]ethanol;2-methylpropan-2-amine Chemical compound CC(C)(C)N.OCCOCCOCCO YSVQAQXTVLLNBA-UHFFFAOYSA-N 0.000 description 1
- 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 description 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- PGOFJDZYVIIGGD-UHFFFAOYSA-N 3-(tert-butylamino)propan-1-ol Chemical compound CC(C)(C)NCCCO PGOFJDZYVIIGGD-UHFFFAOYSA-N 0.000 description 1
- OILJIEKQCVHNMM-UHFFFAOYSA-N 4-tert-butylmorpholine Chemical compound CC(C)(C)N1CCOCC1 OILJIEKQCVHNMM-UHFFFAOYSA-N 0.000 description 1
- 229920005831 Autopour® Polymers 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 101000863856 Homo sapiens Shiftless antiviral inhibitor of ribosomal frameshifting protein Proteins 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical class [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 125000002015 acyclic group Chemical group 0.000 description 1
- 125000003158 alcohol group Chemical group 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000003795 desorption Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000013505 freshwater Substances 0.000 description 1
- 239000002737 fuel gas Substances 0.000 description 1
- 238000002309 gasification Methods 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 125000005350 hydroxycycloalkyl group Chemical group 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- UUORTJUPDJJXST-UHFFFAOYSA-N n-(2-hydroxyethyl)prop-2-enamide Chemical compound OCCNC(=O)C=C UUORTJUPDJJXST-UHFFFAOYSA-N 0.000 description 1
- UGGUOQMUQUMCJX-UHFFFAOYSA-N n-[2-[2-[2-(tert-butylamino)ethoxy]ethoxy]ethyl]-2-methylpropan-2-amine Chemical group CC(C)(C)NCCOCCOCCNC(C)(C)C UGGUOQMUQUMCJX-UHFFFAOYSA-N 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
-
- 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
-
- 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
- B01D53/1493—Selection of liquid materials for use as absorbents
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2252/00—Absorbents, i.e. solvents and liquid materials for gas absorption
- B01D2252/10—Inorganic absorbents
- B01D2252/103—Water
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2252/00—Absorbents, i.e. solvents and liquid materials for gas absorption
- B01D2252/20—Organic absorbents
- B01D2252/202—Alcohols or their derivatives
- B01D2252/2023—Glycols, diols or their derivatives
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2252/00—Absorbents, i.e. solvents and liquid materials for gas absorption
- B01D2252/20—Organic absorbents
- B01D2252/202—Alcohols or their derivatives
- B01D2252/2023—Glycols, diols or their derivatives
- B01D2252/2025—Ethers or esters of alkylene glycols, e.g. ethylene or propylene carbonate
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2252/00—Absorbents, i.e. solvents and liquid materials for gas absorption
- B01D2252/20—Organic absorbents
- B01D2252/204—Amines
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2252/00—Absorbents, i.e. solvents and liquid materials for gas absorption
- B01D2252/50—Combinations of absorbents
- B01D2252/504—Mixtures of two or more absorbents
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2252/00—Absorbents, i.e. solvents and liquid materials for gas absorption
- B01D2252/60—Additives
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02C—CAPTURE, STORAGE, SEQUESTRATION OR DISPOSAL OF GREENHOUSE GASES [GHG]
- Y02C20/00—Capture or disposal of greenhouse gases
- Y02C20/40—Capture or disposal of greenhouse gases of CO2
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T137/00—Fluid handling
- Y10T137/0318—Processes
- Y10T137/0391—Affecting flow by the addition of material or energy
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)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Gas Separation By Absorption (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Carbon And Carbon Compounds (AREA)
- Industrial Gases (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201261610608P | 2012-03-14 | 2012-03-14 | |
| US61/610,608 | 2012-03-14 | ||
| US13/793,298 | 2013-03-11 | ||
| US13/793,298 US9458367B2 (en) | 2012-03-14 | 2013-03-11 | Low temperature transport and storage of amine gas treatment solutions |
| PCT/US2013/030790 WO2013138440A1 (en) | 2012-03-14 | 2013-03-13 | Low temperature transport and storage of aminoether gas treatment solutions |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| RU2014139220A RU2014139220A (ru) | 2016-05-10 |
| RU2614955C2 true RU2614955C2 (ru) | 2017-03-31 |
Family
ID=49156534
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2014139220A RU2614955C2 (ru) | 2012-03-14 | 2013-03-13 | Низкотемпературная транспортировка и хранение аминоэфирных растворов для обработки газа |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US9458367B2 (https=) |
| EP (1) | EP2825287B1 (https=) |
| JP (1) | JP2015516869A (https=) |
| KR (1) | KR101902050B1 (https=) |
| CN (1) | CN104168981B (https=) |
| CA (1) | CA2866974C (https=) |
| IN (1) | IN2014DN07033A (https=) |
| PE (2) | PE20142145A1 (https=) |
| RU (1) | RU2614955C2 (https=) |
| WO (1) | WO2013138440A1 (https=) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2026057367A1 (en) | 2024-09-11 | 2026-03-19 | Basf Se | Transportation and storage of amines solutions for gas treatment |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2003055578A1 (en) * | 2001-12-28 | 2003-07-10 | Diversified Industries Inc. | Solution and method for scavenging sulphur compounds |
| US7115215B2 (en) * | 2001-02-01 | 2006-10-03 | Canwell Enviro-Industries, Ltd. | Method and composition for removing sulfides from hydrocarbon streams |
| EA008970B1 (ru) * | 2003-07-22 | 2007-10-26 | Дау Глобал Текнолоджиз Инк. | Регенерация текучих сред для обработки, содержащих кислый газ |
| WO2007135100A1 (de) * | 2006-05-19 | 2007-11-29 | Basf Se | Vormischung zur herstellung eines absorptionsmittels zum entfernen saurer gase aus fluidströmen |
Family Cites Families (41)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2385704A (en) | 1942-01-22 | 1945-09-25 | Dow Chemical Co | Method of recovering sulphur dioxide |
| NL64177C (https=) | 1943-02-08 | |||
| US3039251A (en) | 1959-10-02 | 1962-06-19 | El Paso Natural Gas Prod | Products and process for purifying gases |
| US3475329A (en) | 1966-03-21 | 1969-10-28 | Phillips Petroleum Co | Absorption of sulfur dioxide from mixtures with sulfolane |
| US3826811A (en) | 1971-07-12 | 1974-07-30 | Union Carbide Canada Ltd | Sulphur removal from natural gas |
| AU506199B2 (en) | 1975-06-26 | 1979-12-20 | Exxon Research And Engineering Company | Absorbtion of co2 from gaseous feeds |
| US4150962A (en) | 1975-12-15 | 1979-04-24 | Uop Inc. | Pretreatment of raw natural gas prior to liquefaction |
| NL190316C (nl) | 1978-03-22 | 1994-01-17 | Shell Int Research | Werkwijze voor het verwijderen van zure gassen uit een gasmengsel. |
| US4471138A (en) | 1982-01-18 | 1984-09-11 | Exxon Research And Engineering Co. | Severely sterically hindered secondary aminoether alcohols |
| US4405581A (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 amino compounds |
| US4405583A (en) | 1982-01-18 | 1983-09-20 | Exxon Research And Engineering Co. | Process for selective removal of H2 S from mixtures containing H22 using di-severely sterically hindered secondary aminoethers |
| 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 |
| US4801308A (en) | 1983-10-03 | 1989-01-31 | Keefer Bowie | Apparatus and process for pressure swing adsorption separation |
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- 2013-03-11 US US13/793,298 patent/US9458367B2/en not_active Expired - Fee Related
- 2013-03-13 KR KR1020147028157A patent/KR101902050B1/ko not_active Expired - Fee Related
- 2013-03-13 WO PCT/US2013/030790 patent/WO2013138440A1/en not_active Ceased
- 2013-03-13 EP EP13712079.6A patent/EP2825287B1/en not_active Not-in-force
- 2013-03-13 RU RU2014139220A patent/RU2614955C2/ru not_active IP Right Cessation
- 2013-03-13 JP JP2015500550A patent/JP2015516869A/ja active Pending
- 2013-03-13 IN IN7033DEN2014 patent/IN2014DN07033A/en unknown
- 2013-03-13 CA CA2866974A patent/CA2866974C/en not_active Expired - Fee Related
- 2013-03-13 PE PE2014001408A patent/PE20142145A1/es active IP Right Grant
- 2013-03-13 CN CN201380013850.9A patent/CN104168981B/zh not_active Expired - Fee Related
- 2013-03-13 PE PE2018003083A patent/PE20190162A1/es unknown
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Also Published As
| Publication number | Publication date |
|---|---|
| EP2825287A1 (en) | 2015-01-21 |
| RU2014139220A (ru) | 2016-05-10 |
| PE20190162A1 (es) | 2019-01-30 |
| US9458367B2 (en) | 2016-10-04 |
| PE20142145A1 (es) | 2015-01-04 |
| JP2015516869A (ja) | 2015-06-18 |
| EP2825287B1 (en) | 2018-01-31 |
| CN104168981B (zh) | 2016-12-28 |
| KR101902050B1 (ko) | 2018-09-27 |
| CA2866974A1 (en) | 2013-09-19 |
| IN2014DN07033A (https=) | 2015-04-10 |
| WO2013138440A1 (en) | 2013-09-19 |
| CN104168981A (zh) | 2014-11-26 |
| CA2866974C (en) | 2018-10-02 |
| KR20140133915A (ko) | 2014-11-20 |
| US20130240047A1 (en) | 2013-09-19 |
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