NO319385B1 - Fremgangsmate for fjerning av karbondioksid til stede i gasser, samt absorbent - Google Patents
Fremgangsmate for fjerning av karbondioksid til stede i gasser, samt absorbent Download PDFInfo
- Publication number
- NO319385B1 NO319385B1 NO19971133A NO971133A NO319385B1 NO 319385 B1 NO319385 B1 NO 319385B1 NO 19971133 A NO19971133 A NO 19971133A NO 971133 A NO971133 A NO 971133A NO 319385 B1 NO319385 B1 NO 319385B1
- Authority
- NO
- Norway
- Prior art keywords
- present
- amine compound
- absorbent
- gases
- aqueous solution
- Prior art date
Links
- 239000007789 gas Substances 0.000 title claims description 78
- 230000002745 absorbent Effects 0.000 title claims description 55
- 239000002250 absorbent Substances 0.000 title claims description 55
- 238000000034 method Methods 0.000 title claims description 36
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 title description 87
- 229910002092 carbon dioxide Inorganic materials 0.000 title description 69
- 239000001569 carbon dioxide Substances 0.000 title description 3
- -1 amine compound Chemical group 0.000 claims description 40
- 239000007864 aqueous solution Substances 0.000 claims description 33
- 238000002485 combustion reaction Methods 0.000 claims description 29
- 125000004432 carbon atom Chemical group C* 0.000 claims description 11
- PPQDYOBQQWPTIS-UHFFFAOYSA-N 2-(diethylamino)acetamide Chemical compound CCN(CC)CC(N)=O PPQDYOBQQWPTIS-UHFFFAOYSA-N 0.000 claims description 9
- 125000000217 alkyl group Chemical group 0.000 claims description 8
- DWGMAIPVJRBOIB-UHFFFAOYSA-N 2-(dimethylamino)-n,n-dimethylacetamide Chemical compound CN(C)CC(=O)N(C)C DWGMAIPVJRBOIB-UHFFFAOYSA-N 0.000 claims description 6
- KFWVHGPZNYEBQI-UHFFFAOYSA-N 2-(tert-butylamino)acetamide Chemical compound CC(C)(C)NCC(N)=O KFWVHGPZNYEBQI-UHFFFAOYSA-N 0.000 claims description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 5
- 150000001875 compounds Chemical class 0.000 claims 3
- 239000000243 solution Substances 0.000 description 47
- 238000010521 absorption reaction Methods 0.000 description 14
- 150000001412 amines Chemical class 0.000 description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 12
- 230000008929 regeneration Effects 0.000 description 12
- 238000011069 regeneration method Methods 0.000 description 12
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 8
- 238000010992 reflux Methods 0.000 description 8
- 238000003795 desorption Methods 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 6
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 6
- MIJDSYMOBYNHOT-UHFFFAOYSA-N 2-(ethylamino)ethanol Chemical compound CCNCCO MIJDSYMOBYNHOT-UHFFFAOYSA-N 0.000 description 5
- 239000002253 acid Substances 0.000 description 5
- 238000005262 decarbonization Methods 0.000 description 5
- 238000003786 synthesis reaction Methods 0.000 description 5
- BFSVOASYOCHEOV-UHFFFAOYSA-N 2-diethylaminoethanol Chemical compound CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 description 4
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 4
- OPKOKAMJFNKNAS-UHFFFAOYSA-N N-methylethanolamine Chemical compound CNCCO OPKOKAMJFNKNAS-UHFFFAOYSA-N 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- 239000000498 cooling water Substances 0.000 description 4
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 4
- CRVGTESFCCXCTH-UHFFFAOYSA-N methyl diethanolamine Chemical compound OCCN(C)CCO CRVGTESFCCXCTH-UHFFFAOYSA-N 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 229940058020 2-amino-2-methyl-1-propanol Drugs 0.000 description 3
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 3
- CBTVGIZVANVGBH-UHFFFAOYSA-N aminomethyl propanol Chemical compound CC(C)(N)CO CBTVGIZVANVGBH-UHFFFAOYSA-N 0.000 description 3
- 239000003345 natural gas Substances 0.000 description 3
- PTHDBHDZSMGHKF-UHFFFAOYSA-N 2-piperidin-2-ylethanol Chemical compound OCCC1CCCCN1 PTHDBHDZSMGHKF-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 2
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 2
- 150000001721 carbon Chemical group 0.000 description 2
- 238000003889 chemical engineering Methods 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 230000001172 regenerating effect Effects 0.000 description 2
- KODLUXHSIZOKTG-UHFFFAOYSA-N 1-aminobutan-2-ol Chemical compound CCC(O)CN KODLUXHSIZOKTG-UHFFFAOYSA-N 0.000 description 1
- CEXOTARNUNKHAK-UHFFFAOYSA-N 1-n,3-dimethylbutane-1,3-diamine Chemical compound CNCCC(C)(C)N CEXOTARNUNKHAK-UHFFFAOYSA-N 0.000 description 1
- NSMWYRLQHIXVAP-UHFFFAOYSA-N 2,5-dimethylpiperazine Chemical compound CC1CNC(C)CN1 NSMWYRLQHIXVAP-UHFFFAOYSA-N 0.000 description 1
- GIAFURWZWWWBQT-UHFFFAOYSA-N 2-(2-aminoethoxy)ethanol Chemical compound NCCOCCO GIAFURWZWWWBQT-UHFFFAOYSA-N 0.000 description 1
- LJDSTRZHPWMDPG-UHFFFAOYSA-N 2-(butylamino)ethanol Chemical compound CCCCNCCO LJDSTRZHPWMDPG-UHFFFAOYSA-N 0.000 description 1
- DUTNJWYCYGWDHQ-UHFFFAOYSA-N 2-(diethylamino)-2-methylpropanamide Chemical compound CCN(CC)C(C)(C)C(N)=O DUTNJWYCYGWDHQ-UHFFFAOYSA-N 0.000 description 1
- UGYQLLBBRLDEHY-UHFFFAOYSA-N 2-(diethylamino)propanamide Chemical compound CCN(CC)C(C)C(N)=O UGYQLLBBRLDEHY-UHFFFAOYSA-N 0.000 description 1
- FTKUJZVWJCGMRA-UHFFFAOYSA-N 2-(ethylamino)-2-methylpropanamide Chemical compound CCNC(C)(C)C(N)=O FTKUJZVWJCGMRA-UHFFFAOYSA-N 0.000 description 1
- SNFFHBJWQFQMBC-UHFFFAOYSA-N 2-(ethylamino)acetamide Chemical compound CCNCC(N)=O SNFFHBJWQFQMBC-UHFFFAOYSA-N 0.000 description 1
- RILLZYSZSDGYGV-UHFFFAOYSA-N 2-(propan-2-ylamino)ethanol Chemical compound CC(C)NCCO RILLZYSZSDGYGV-UHFFFAOYSA-N 0.000 description 1
- ZIOBGZDFMKCKGZ-UHFFFAOYSA-N 2-amino-2-methylpropanamide Chemical compound CC(C)(N)C(N)=O ZIOBGZDFMKCKGZ-UHFFFAOYSA-N 0.000 description 1
- HEZDWTXSXRFPEP-UHFFFAOYSA-N 2-amino-n,2-dimethylpropanamide Chemical compound CNC(=O)C(C)(C)N HEZDWTXSXRFPEP-UHFFFAOYSA-N 0.000 description 1
- HQMLIDZJXVVKCW-UHFFFAOYSA-N 2-aminopropanamide Chemical compound CC(N)C(N)=O HQMLIDZJXVVKCW-UHFFFAOYSA-N 0.000 description 1
- 229940013085 2-diethylaminoethanol Drugs 0.000 description 1
- JOMNTHCQHJPVAZ-UHFFFAOYSA-N 2-methylpiperazine Chemical compound CC1CNCCN1 JOMNTHCQHJPVAZ-UHFFFAOYSA-N 0.000 description 1
- WFCSWCVEJLETKA-UHFFFAOYSA-N 2-piperazin-1-ylethanol Chemical compound OCCN1CCNCC1 WFCSWCVEJLETKA-UHFFFAOYSA-N 0.000 description 1
- PPUXNQHLNOVQRG-UHFFFAOYSA-N 3-(ethylamino)propanamide Chemical compound CCNCCC(N)=O PPUXNQHLNOVQRG-UHFFFAOYSA-N 0.000 description 1
- XQVOIOIPSWCLBC-UHFFFAOYSA-N 3-N,3-N-diethyl-3-methylbutane-1,3-diamine Chemical compound CCN(CC)C(C)(C)CCN XQVOIOIPSWCLBC-UHFFFAOYSA-N 0.000 description 1
- RTHPUFIOGJLOQA-UHFFFAOYSA-N 3-N-ethyl-3-methylbutane-1,3-diamine Chemical compound CCNC(C)(C)CCN RTHPUFIOGJLOQA-UHFFFAOYSA-N 0.000 description 1
- WSDOLNVCEVYCJQ-UHFFFAOYSA-N 3-methylbutane-1,3-diamine Chemical compound CC(C)(N)CCN WSDOLNVCEVYCJQ-UHFFFAOYSA-N 0.000 description 1
- IMBPNEGZDBFLBN-UHFFFAOYSA-N 3-n-ethylbutane-1,3-diamine Chemical compound CCNC(C)CCN IMBPNEGZDBFLBN-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 239000003125 aqueous solvent Substances 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- LVTYICIALWPMFW-UHFFFAOYSA-N diisopropanolamine Chemical compound CC(O)CNCC(C)O LVTYICIALWPMFW-UHFFFAOYSA-N 0.000 description 1
- 229940043276 diisopropanolamine Drugs 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000008246 gaseous mixture Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 150000004885 piperazines Chemical class 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 1
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 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
- 125000001302 tertiary amino group Chemical group 0.000 description 1
- 238000005406 washing 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
- B01D53/1493—Selection of liquid materials for use as absorbents
-
- 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
- B01D53/1475—Removing carbon dioxide
-
- 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
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/20—Air quality improvement or preservation, e.g. vehicle emission control or emission reduction by using catalytic converters
-
- 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
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)
- Treating Waste Gases (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
- Carbon And Carbon Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP06263596A JP3761960B2 (ja) | 1996-03-19 | 1996-03-19 | ガス中の二酸化炭素の除去方法 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO971133D0 NO971133D0 (no) | 1997-03-12 |
| NO971133L NO971133L (no) | 1997-09-22 |
| NO319385B1 true NO319385B1 (no) | 2005-08-08 |
Family
ID=13205991
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO19971133A NO319385B1 (no) | 1996-03-19 | 1997-03-12 | Fremgangsmate for fjerning av karbondioksid til stede i gasser, samt absorbent |
Country Status (7)
| Country | Link |
|---|---|
| US (2) | US5904908A (de) |
| EP (1) | EP0796646B1 (de) |
| JP (1) | JP3761960B2 (de) |
| CA (1) | CA2200130C (de) |
| DE (1) | DE69726039T2 (de) |
| DK (1) | DK0796646T3 (de) |
| NO (1) | NO319385B1 (de) |
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3761960B2 (ja) * | 1996-03-19 | 2006-03-29 | 仁美 鈴木 | ガス中の二酸化炭素の除去方法 |
| RU2191621C2 (ru) * | 1998-04-06 | 2002-10-27 | Ниппон Ниюказаи Ко., Лтд. | Способ регенерации жидкости, абсорбирующей кислый газ, содержащей метилдиэтаноламин и производное пиперазина низших алкилов |
| FR2777802B1 (fr) * | 1998-04-22 | 2000-06-23 | Elf Exploration Prod | Procede regeneratif de desacidification d'un gaz renfermant du co2 ainsi que des hydrocarbures liquides, a l'aide d'un liquide absorbant a base de methyldiethanolamine activee |
| DE19828977A1 (de) * | 1998-06-29 | 1999-12-30 | Basf Ag | Verfahren zur Entfernung saurer Gasbestandteile aus Gasen |
| US6270739B1 (en) * | 2000-06-16 | 2001-08-07 | Eastman Chemical Company | Process for the removal of carbon dioxide from 3,4-epoxy-1-butene process recycle streams |
| US6582498B1 (en) | 2001-05-04 | 2003-06-24 | Battelle Memorial Institute | Method of separating carbon dioxide from a gas mixture using a fluid dynamic instability |
| CA2353307A1 (fr) | 2001-07-13 | 2003-01-13 | Carmen Parent | Appareil et procede pour le traitement des effluents gazeux |
| CA2405635A1 (en) | 2002-09-27 | 2004-03-27 | C02 Solution Inc. | A process and a plant for the production of useful carbonated species and for the recycling of carbon dioxide emissions from power plants |
| TWI313186B (en) * | 2003-02-10 | 2009-08-11 | Shell Int Research | Removing natural gas liquids from a gaseous natural gas stream |
| US7832412B2 (en) * | 2004-10-25 | 2010-11-16 | Phillip Morris Usa Inc. | Surface modified adsorbents and use thereof |
| AU2006217575B2 (en) | 2005-02-24 | 2010-12-23 | Co2 Solutions Inc. | An improved CO2 absorption solution |
| JP5230080B2 (ja) * | 2006-06-06 | 2013-07-10 | 三菱重工業株式会社 | 吸収液、ｃｏ２の除去装置及び方法 |
| CA2598388C (en) * | 2006-08-23 | 2012-11-27 | University Of Regina | Method for capturing carbon dioxide from gas streams |
| JP5215595B2 (ja) * | 2007-06-18 | 2013-06-19 | 三菱重工業株式会社 | 吸収液、吸収液を用いたｃｏ２又はｈ２ｓ除去装置及び方法 |
| DE102007062413B3 (de) * | 2007-12-20 | 2009-09-10 | Conera Process Solutions Gmbh | Verfahren und Vorrichtung zur Wiederaufbereitung von CO2-haltigen Abgasen |
| CA2711435C (en) * | 2008-02-22 | 2012-10-09 | Mitsubishi Heavy Industries, Ltd. | Co2 recovery apparatus and co2 recovery method |
| JP5351728B2 (ja) * | 2009-12-03 | 2013-11-27 | 三菱重工業株式会社 | Ｃｏ２回収装置およびｃｏ２回収方法 |
| JP5371734B2 (ja) * | 2009-12-25 | 2013-12-18 | 三菱重工業株式会社 | Ｃｏ２回収装置およびｃｏ２回収方法 |
| US8795618B2 (en) * | 2010-03-26 | 2014-08-05 | Babcock & Wilcox Power Generation Group, Inc. | Chemical compounds for the removal of carbon dioxide from gases |
| DE102010019330B4 (de) | 2010-05-05 | 2013-11-07 | Ecoloop Gmbh | Verfahren zur Umwandlung von Carbonaten in Oxide |
| CN101829475B (zh) * | 2010-05-06 | 2012-12-12 | 合肥工业大学 | 一种多元胺类酰胺烟气脱硫剂及其制备方法 |
| JP5527095B2 (ja) * | 2010-08-09 | 2014-06-18 | 株式会社Ｉｈｉ | 二酸化炭素の回収方法及び回収装置 |
| AU2011296309B2 (en) | 2010-09-02 | 2014-11-20 | The Regents Of The University Of California | Method and system for capturing carbon dioxide and/or sulfur dioxide from gas stream |
| US8765083B2 (en) * | 2010-11-19 | 2014-07-01 | Nalco Company | Acid gas absorbent composition |
| NO20110974A1 (no) * | 2011-07-05 | 2013-01-07 | Aker Clean Carbon As | Utslippskontroll |
| JP5450540B2 (ja) | 2011-09-12 | 2014-03-26 | 株式会社日立製作所 | Ｃｏ２回収装置を備えたボイラーの熱回収システム |
| US8545782B1 (en) * | 2012-10-16 | 2013-10-01 | Mitsubishi Heavy Industries, Ltd. | CO2 recovery apparatus and CO2 recovery method |
| JP6841676B2 (ja) | 2017-01-31 | 2021-03-10 | 三菱重工エンジニアリング株式会社 | 複合アミン吸収液、ｃｏ２又はｈ２ｓ又はその双方の除去装置及び方法 |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1467942A (fr) * | 1965-12-23 | 1967-02-03 | Procédé de préparation de dérivés nu-disubstitués de l'aminoacétamide et nouveaux dérivés de ce type | |
| DE1546239A1 (de) * | 1966-12-31 | 1969-11-27 | Basf Ag | Verfahren zum Bleichen |
| DE2534018A1 (de) * | 1975-07-30 | 1977-02-17 | Basf Ag | Verfahren zur abtrennung von co tief 2 und/oder h tief 2 s aus gasen, die diese bestandteile enthalten |
| US4094957A (en) * | 1976-12-14 | 1978-06-13 | Exxon Research & Engineering Co. | Process for removing acid gases with hindered amines and amino acids |
| DE3111199A1 (de) * | 1981-03-21 | 1982-09-30 | Basf Ag, 6700 Ludwigshafen | Kationische phthalocyaninfarbstoffe und deren verwendung |
| US4364915A (en) * | 1981-05-21 | 1982-12-21 | Procon International Inc. | Process for recovery of carbon dioxide from flue gas |
| FR2539415B1 (fr) * | 1983-01-14 | 1985-09-13 | Adir | Derives de la d-2 imidazoline, leur preparation et leur application en therapeutique |
| IN164027B (de) * | 1984-03-29 | 1988-12-31 | Basf Ag | |
| US4766229A (en) * | 1985-01-18 | 1988-08-23 | Agency Of Industrial Science And Technology | Materials for gas separation |
| US4742068A (en) * | 1986-06-09 | 1988-05-03 | Mcneilab, Inc. | Dihydropyridine compounds having 1,4,4-trisubstitution useful as antihypertensive agents |
| 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 |
| US5102777A (en) * | 1990-02-01 | 1992-04-07 | Ardrox Inc. | Resist stripping |
| JP3357453B2 (ja) * | 1993-09-10 | 2002-12-16 | 花王株式会社 | 液体柔軟仕上剤組成物並びに新規第４級アンモニウム塩並びに該塩の製造法 |
| DE19548008A1 (de) * | 1995-12-21 | 1996-05-30 | Linde Ag | Verfahren zur selektiven Entfernung anorganischer und/oder organischer Schwefelverbindungen |
| JP3761960B2 (ja) * | 1996-03-19 | 2006-03-29 | 仁美 鈴木 | ガス中の二酸化炭素の除去方法 |
-
1996
- 1996-03-19 JP JP06263596A patent/JP3761960B2/ja not_active Expired - Fee Related
-
1997
- 1997-03-12 NO NO19971133A patent/NO319385B1/no not_active IP Right Cessation
- 1997-03-13 US US08/816,646 patent/US5904908A/en not_active Expired - Fee Related
- 1997-03-17 EP EP97301767A patent/EP0796646B1/de not_active Expired - Lifetime
- 1997-03-17 CA CA002200130A patent/CA2200130C/en not_active Expired - Fee Related
- 1997-03-17 DK DK97301767T patent/DK0796646T3/da active
- 1997-03-17 DE DE69726039T patent/DE69726039T2/de not_active Expired - Lifetime
-
1998
- 1998-06-29 US US09/106,267 patent/US6051161A/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| DE69726039D1 (de) | 2003-12-18 |
| EP0796646B1 (de) | 2003-11-12 |
| NO971133L (no) | 1997-09-22 |
| DK0796646T3 (da) | 2004-02-16 |
| CA2200130A1 (en) | 1997-09-19 |
| JPH09253446A (ja) | 1997-09-30 |
| US5904908A (en) | 1999-05-18 |
| EP0796646A1 (de) | 1997-09-24 |
| JP3761960B2 (ja) | 2006-03-29 |
| DE69726039T2 (de) | 2004-08-26 |
| US6051161A (en) | 2000-04-18 |
| NO971133D0 (no) | 1997-03-12 |
| CA2200130C (en) | 2000-12-05 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| NO319385B1 (no) | Fremgangsmate for fjerning av karbondioksid til stede i gasser, samt absorbent | |
| EP0705637B1 (de) | Verfahren zum Eliminieren von Kohlendioxyd aus Gasen | |
| CA2657993C (en) | Absorbent liquid, and apparatus and method for removing co2 or h2s from gas with use of absorbent liquid | |
| RU2402373C2 (ru) | Способ рекуперации двуокиси углерода | |
| EP0875280B1 (de) | Verfahren zur Abscheidung von Kohlendioxid aus Verbrennungsabgasen | |
| KR0125591B1 (ko) | 연소배기가스중의 이산화탄소를 제거하는 방법 | |
| US5603908A (en) | Process for removing carbon dioxide from combustion gases | |
| DK2300127T3 (en) | ABSORPENT AND PROCEDURE FOR THE REMOVAL OF ACID GASES FROM LIQUID FLOWS, PARTICULARLY FROM Flue gases | |
| NO334582B1 (no) | Fremgangsmåte for å fjerne karbondioksid fra gassblandinger og en absrbentvæske | |
| JP2009006275A (ja) | 排ガス中の二酸化炭素を効率的に回収する方法 | |
| CA2924825A1 (en) | Gas sweetening solvents containing quaternary ammonium salts | |
| NO159243B (no) | Fremgangsmaate for fjerning av hydrogensulfid fra gassblandinger. | |
| KR102037878B1 (ko) | 이산화탄소 흡수제와 이를 이용한 이산화탄소의 분리방법 | |
| CA2083684A1 (en) | Process and apparatus for removing acid gas from a gaseous composition | |
| CA2617610C (en) | Polyalkyleneacrylamide salt for acid gas scrubbing process | |
| JP5039276B2 (ja) | 吸収液、吸収液を用いたガス中のｃｏ２又はｈ２ｓ除去装置及び方法 | |
| JP2007000702A (ja) | 吸収液、ｃｏ２又はｈ２ｓ又はその双方の除去装置及び除去方法 | |
| JP5627534B2 (ja) | 吸収液、吸収液を用いたガス中のｃｏ２又はｈ２ｓ除去装置及び方法 | |
| US20150314230A1 (en) | Absorbent solution based on amines belonging to the n-alkylhydroxypiperidine family and method for removing acid compounds from a gaseous effluent with such a solution | |
| NO172179B (no) | Diaminoeter til bruk for fjerning av h2s fra vanligvis gassformige blandinger, samt deres fremstilling |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM1K | Lapsed by not paying the annual fees |