EP1303344A2 - Recuperation de co 2? tres pur dans des fumees - Google Patents
Recuperation de co 2? tres pur dans des fumeesInfo
- Publication number
- EP1303344A2 EP1303344A2 EP01967856A EP01967856A EP1303344A2 EP 1303344 A2 EP1303344 A2 EP 1303344A2 EP 01967856 A EP01967856 A EP 01967856A EP 01967856 A EP01967856 A EP 01967856A EP 1303344 A2 EP1303344 A2 EP 1303344A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- absorber
- desorber
- depleted
- solvent
- stream
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- 238000000034 method Methods 0.000 title claims abstract description 50
- 239000003546 flue gas Substances 0.000 title claims abstract description 47
- 238000011084 recovery Methods 0.000 title claims abstract description 14
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 title claims description 27
- 238000009434 installation Methods 0.000 title claims description 16
- 239000002904 solvent Substances 0.000 claims abstract description 78
- 239000006096 absorbing agent Substances 0.000 claims abstract description 42
- 239000007789 gas Substances 0.000 claims abstract description 42
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 claims abstract description 12
- 239000012190 activator Substances 0.000 claims abstract description 10
- CRVGTESFCCXCTH-UHFFFAOYSA-N methyl diethanolamine Chemical compound OCCN(C)CCO CRVGTESFCCXCTH-UHFFFAOYSA-N 0.000 claims abstract description 9
- 238000010521 absorption reaction Methods 0.000 claims abstract description 7
- 238000003795 desorption Methods 0.000 claims abstract description 7
- 239000007864 aqueous solution Substances 0.000 claims abstract description 3
- 238000001914 filtration Methods 0.000 claims description 15
- 229910052799 carbon Inorganic materials 0.000 claims description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 11
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 9
- 239000001301 oxygen Substances 0.000 claims description 9
- 229910052760 oxygen Inorganic materials 0.000 claims description 9
- 238000002485 combustion reaction Methods 0.000 claims description 8
- 150000002500 ions Chemical class 0.000 claims description 7
- 238000005342 ion exchange Methods 0.000 claims description 4
- 239000012530 fluid Substances 0.000 claims description 3
- HXKKHQJGJAFBHI-UHFFFAOYSA-N 1-aminopropan-2-ol Chemical compound CC(O)CN HXKKHQJGJAFBHI-UHFFFAOYSA-N 0.000 claims description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical group NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 claims description 2
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims description 2
- SLINHMUFWFWBMU-UHFFFAOYSA-N Triisopropanolamine Chemical compound CC(O)CN(CC(C)O)CC(C)O SLINHMUFWFWBMU-UHFFFAOYSA-N 0.000 claims description 2
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 claims description 2
- LVTYICIALWPMFW-UHFFFAOYSA-N diisopropanolamine Chemical compound CC(O)CNCC(C)O LVTYICIALWPMFW-UHFFFAOYSA-N 0.000 claims description 2
- 229940043276 diisopropanolamine Drugs 0.000 claims description 2
- 235000013305 food Nutrition 0.000 abstract description 21
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 103
- 239000000243 solution Substances 0.000 description 18
- 150000003839 salts Chemical class 0.000 description 9
- PVXVWWANJIWJOO-UHFFFAOYSA-N 1-(1,3-benzodioxol-5-yl)-N-ethylpropan-2-amine Chemical compound CCNC(C)CC1=CC=C2OCOC2=C1 PVXVWWANJIWJOO-UHFFFAOYSA-N 0.000 description 8
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 8
- QMMZSJPSPRTHGB-UHFFFAOYSA-N MDEA Natural products CC(C)CCCCC=CCC=CC(O)=O QMMZSJPSPRTHGB-UHFFFAOYSA-N 0.000 description 7
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 5
- 238000010586 diagram Methods 0.000 description 5
- 230000008929 regeneration Effects 0.000 description 5
- 238000011069 regeneration method Methods 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- 239000005864 Sulphur Substances 0.000 description 4
- 150000001450 anions Chemical class 0.000 description 4
- 239000007857 degradation product Substances 0.000 description 4
- 239000003345 natural gas Substances 0.000 description 4
- 229910017464 nitrogen compound Inorganic materials 0.000 description 4
- 150000002830 nitrogen compounds Chemical class 0.000 description 4
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
- 230000002745 absorbent Effects 0.000 description 3
- 239000002250 absorbent Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- 238000011144 upstream manufacturing Methods 0.000 description 3
- LJDSTRZHPWMDPG-UHFFFAOYSA-N 2-(butylamino)ethanol Chemical compound CCCCNCCO LJDSTRZHPWMDPG-UHFFFAOYSA-N 0.000 description 2
- OPKOKAMJFNKNAS-UHFFFAOYSA-N N-methylethanolamine Chemical compound CNCCO OPKOKAMJFNKNAS-UHFFFAOYSA-N 0.000 description 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 2
- 238000009825 accumulation Methods 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000000498 cooling water Substances 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 239000002803 fossil fuel Substances 0.000 description 2
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 239000010413 mother solution Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- KODLUXHSIZOKTG-UHFFFAOYSA-N 1-aminobutan-2-ol Chemical compound CCC(O)CN KODLUXHSIZOKTG-UHFFFAOYSA-N 0.000 description 1
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
- NSMWYRLQHIXVAP-UHFFFAOYSA-N 2,5-dimethylpiperazine Chemical compound CC1CNC(C)CN1 NSMWYRLQHIXVAP-UHFFFAOYSA-N 0.000 description 1
- MIJDSYMOBYNHOT-UHFFFAOYSA-N 2-(ethylamino)ethanol Chemical compound CCNCCO MIJDSYMOBYNHOT-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
- JOMNTHCQHJPVAZ-UHFFFAOYSA-N 2-methylpiperazine Chemical compound CC1CNCCN1 JOMNTHCQHJPVAZ-UHFFFAOYSA-N 0.000 description 1
- CJNRGSHEMCMUOE-UHFFFAOYSA-N 2-piperidin-1-ylethanamine Chemical compound NCCN1CCCCC1 CJNRGSHEMCMUOE-UHFFFAOYSA-N 0.000 description 1
- PTHDBHDZSMGHKF-UHFFFAOYSA-N 2-piperidin-2-ylethanol Chemical compound OCCC1CCCCN1 PTHDBHDZSMGHKF-UHFFFAOYSA-N 0.000 description 1
- SOYBEXQHNURCGE-UHFFFAOYSA-N 3-ethoxypropan-1-amine Chemical compound CCOCCCN SOYBEXQHNURCGE-UHFFFAOYSA-N 0.000 description 1
- FAXDZWQIWUSWJH-UHFFFAOYSA-N 3-methoxypropan-1-amine Chemical compound COCCCN FAXDZWQIWUSWJH-UHFFFAOYSA-N 0.000 description 1
- UVLSCMIEPPWCHZ-UHFFFAOYSA-N 3-piperazin-1-ylpropan-1-amine Chemical compound NCCCN1CCNCC1 UVLSCMIEPPWCHZ-UHFFFAOYSA-N 0.000 description 1
- JMUCXULQKPWSTJ-UHFFFAOYSA-N 3-piperidin-1-ylpropan-1-amine Chemical compound NCCCN1CCCCC1 JMUCXULQKPWSTJ-UHFFFAOYSA-N 0.000 description 1
- 229910000975 Carbon steel Inorganic materials 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- 125000005263 alkylenediamine group Chemical group 0.000 description 1
- LHIJANUOQQMGNT-UHFFFAOYSA-N aminoethylethanolamine Chemical compound NCCNCCO LHIJANUOQQMGNT-UHFFFAOYSA-N 0.000 description 1
- IMUDHTPIFIBORV-UHFFFAOYSA-N aminoethylpiperazine Chemical compound NCCN1CCNCC1 IMUDHTPIFIBORV-UHFFFAOYSA-N 0.000 description 1
- 239000003957 anion exchange resin Substances 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 235000013405 beer Nutrition 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000010962 carbon steel Substances 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000003729 cation exchange resin Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000002826 coolant Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- IUNMPGNGSSIWFP-UHFFFAOYSA-N dimethylaminopropylamine Chemical compound CN(C)CCCN IUNMPGNGSSIWFP-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- DDRPCXLAQZKBJP-UHFFFAOYSA-N furfurylamine Chemical compound NCC1=CC=CO1 DDRPCXLAQZKBJP-UHFFFAOYSA-N 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- GKQPCPXONLDCMU-CCEZHUSRSA-N lacidipine Chemical compound CCOC(=O)C1=C(C)NC(C)=C(C(=O)OCC)C1C1=CC=CC=C1\C=C\C(=O)OC(C)(C)C GKQPCPXONLDCMU-CCEZHUSRSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005374 membrane filtration Methods 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000003595 mist Substances 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000012797 qualification Methods 0.000 description 1
- 235000014214 soft drink Nutrition 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
- RAOIDOHSFRTOEL-UHFFFAOYSA-N tetrahydrothiophene Chemical compound C1CCSC1 RAOIDOHSFRTOEL-UHFFFAOYSA-N 0.000 description 1
- 229930192474 thiophene Natural products 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
- B01D53/1475—Removing carbon dioxide
-
- 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
- B01D53/34—Chemical or biological purification of waste gases
- B01D53/46—Removing components of defined structure
- B01D53/62—Carbon oxides
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B32/00—Carbon; Compounds thereof
- C01B32/50—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
- 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/151—Reduction of greenhouse gas [GHG] emissions, e.g. CO2
Definitions
- CO 2 has a multiplicity of industrial applications.
- CO 2 is used for, inter alia, carbonating soft drinks, beers and mineral water and the rapid freezing of foods.
- the requirements imposed by the food industry on the purity of the CO2 to be used are high.
- CO 2 product that meets these requirements is hereinafter referred to as food grade CO 2 .
- CO 2 of (very) high purity is required; such as various analytical and medical applications and use as a coolant. Because of the stringent requirements imposed on food grade and high purity CO 2 , there is a shortage, despite the large quantities that are produced.
- CO2 recovery takes place on a large scale in ammonia processes. By further purifying this CO2 it can be made suitable for use in the food industry. Since there are not always ammonia plants in the vicinity of the numerous areas where there is a demand for CO2, it is not possible to meet the entire demand in this way.
- CO2 Another method that is used to produce CO2 is the controlled combustion of fossil fuels. With these systems a CO2-rich gas must first be generated in order to be able to recover the CO2 from this.
- CO2 can be recovered from gas streams by means of membrane filtration techniques.
- membrane filtration techniques it is not possible with this technology to meet the specifications which apply for food grade and high purity.
- the other disadvantages are high investment costs and operational costs.
- Another option is recovery of CO2 by means of cryogenic separation. With this technique upstream separation of the impurities is necessary in order to obtain high purity.
- US 4 477 419 describes a process for the recovery of CO2 from gas that contains CO2, oxygen and/or sulphur compounds, an aqueous alkanolamine solution in combination with copper as an absorbent.
- the degradation products of the solvent can be removed by an active carbon bed, mechanical filter and an anion exchange resin.
- US 4 537 753 describes a process for the removal of CO2 and H2S from natural gas with an aqueous absorption fluid that contains methyldiethanolamine.
- the solvent is regenerated by flashing.
- the aim of the present invention is therefore to provide a method for the recovery of CO2 from flue gases, wherein the recovered CO2 can be used as food grade or high purity CO2.
- the invention provides a method for the recovery of very pure CO2 from flue gases, which method comprises the following steps: a) absorption of CO2 from the flue gases in a solvent in an absorber, a CO2-depleted gas stream and a CO2-rich solvent stream leaving the absorber; b) desorption of the absorbed CO2 in a desorber, a CO2-rich gas stream and a CO2- depleted solvent stream leaving the desorber; wherein the solvent used is an aqueous solution that contains an alkanolamine and an activator.
- the alkanolamine is chosen from monoethanolamine, diethanolamine, triethanolamine, methyldiethanolamine, monoisopropanolamine, diisopropanolamine and triisopropanolamine.
- Methyldiethanolamine (CH3N(CH2CH2OH)2), hereinafter designated MDEA, is used in particular.
- MDEA and activator combination is generally designated as aMDEA.
- the alkanolamine concentration in water is 5 to 80 wt.%, preferably 40 to 60 wt.%.
- the activator used can be any activator suitable for such solvents.
- activators are: polyalkylenepolyamines, in particular diethylenetriamine, triethylenetetramine, tetraethylenepentamine and dipropylenetriamine; alkylenediamines and cycloalkylenediamines, in particular hexamethylenediamine, aminoethylethanolamine, dimethylaminopropylamine and diamino-l,2-cyclohexane, heterocyclic aminoalkyl derivatives, in particular piperazine, piperidine, furan, tetrahydrofuran, thiophene and tetrahydrothiophene, aminoethylpiperazine, aminopropyl- piperazine, 2-methylpiperazine, 2,5-dimethylpiperazine, aminoethylpiperidine, aminopropylpiperidine, 2-piperidine-ethanol and furfurylamine; alkoxylalkylamines, in particular methoxypropylamine and ethoxypropylamine, and alkyl
- Piperazine is preferably used.
- the activator concentration is 1 to 20 wt.%, preferably 2 - 8 wt.%, in the undiluted mother solution.
- This mother solution which in general will also contain MDEA, is generally diluted 0 to 4 times, preferably 1.5 to 3 times, with water before it is fed to the absorber.
- CO2 of very high purity also referred to in this text as high purity or food grade CO 2
- CO 2 of a quality such that it can be used as such in the food industry.
- Food grade CO must contain at least 99.5 % (V/V) CO 2 .
- the method according to the invention has broad applicability for the recovery of food grade and high purity CO2 from flue gases.
- the homogeneous geographic spread of the locations of, for example, power stations now offers the possibility for producing food grade CO2 from the flue gases close to the outlet in any region where CO2 is sold.
- the construction of installations for the production of CO2 in the vicinity of, for example, the food industry is therefore not necessary.
- the requisite energy costs for absorbing and desorbing CO2 with the solvent used are low.
- the energy costs are consequently appreciably lower than the energy costs which are required when conventional solvents such as potassium carbonate are used.
- the operational costs are lowered by the prevention of accumulation of heat stable salts and other substances in the solvent circuit, by purification of the solvent using active carbon filtration and ion exchange, as will be described below.
- the degradation problems of the solvent are restricted by a good choice of solvent.
- flue gases are understood to be the off-gases from the combustion of carbon-containing substances. Examples of these are the flue gases from power stations or flue gases originating from combined heat and power plants, gas turbines or utility centres.
- Step a) of the method according to the invention takes place in an absorber, a CO2- depleted gas stream and a CO2-rich solvent stream leaving the absorber.
- contact between solvent and flue gas in the absorber takes place in counter-current.
- the absorber is in general a reactive absorber.
- the temperature in the absorber is 10 to 100 °C, preferably
- Step b) takes place in a desorber.
- the CO2 is liberated from the solvent under the influence of heat. Absorbed impurities such as SO2 and NO x are not desorbed.
- a CO2-rich gas stream and a CO2-depleted solvent stream leave the desorber.
- the CO2- depleted solvent stream is returned to the absorber.
- the CO2-rich gas stream that leaves the desorber is preferably cooled, after which some condensed fluid is separated off and returned to the desorber.
- the desorber is a packed column in which the CO2 is removed from the solvent counter-currently.
- the temperature in the desorber is generally 80 to 120 °C, in particular 95 to 110 °C. According to a preferred embodiment of the invention heat is exchanged between the
- the CO2-rich solvent stream that leaves the absorber and the CO2-depleted solvent stream that leaves the desorber and is returned to the absorber An appreciable saving in the quantity of steam and cooling water required can be achieved by this means.
- the filtration step comprises, successively, a first mechanical filter, an active carbon filter and a second mechanical filter.
- the first filter is preferably a cartridge filter that removes particles > approx. 5 ⁇ m. The efficiency is higher than 99 %.
- the second filter is likewise preferably a cartridge filter that removes particles > approx. 10 ⁇ m and has an efficiency higher than 99 %.
- At least a portion of the CO2-depleted solvent stream which has been subjected to the filtration step is subjected to ion exchange before it is returned to the absorber.
- a cationic ion exchange resin is used.
- heat stable salts can be removed with this method.
- These heat stable salts are alkanolamine salts, in particular of MDEA, which cannot be regenerated by means of heat (such as steam stripping). These salts lower the efficiency of the treatment with
- MDEA MDEA.
- the MDEA salts lower the availability of MDEA for absorption of CO2. These salts can also give rise to corrosion in equipment made of carbon steel.
- the residual amount of oxygen in the flue gas is combusted using a carbon-containing gas, such as natural gas, before the flue gas is fed to the absorber.
- a carbon-containing gas such as natural gas
- the present invention also provides an installation for carrying out the abovementioned process, which installation comprises: an absorber, which absorber is provided with a feed for flue gases, a feed for a solvent for CO2, a discharge for a CO2-depleted gas stream, a discharge for a CO2-rich solvent stream and a feed for make-up water; a desorber, provided with a feed for the CO2-rich solvent stream, a discharge for CO2-rich gas stream and a discharge for a CO 2 -depleted solvent stream.
- the installation is provided with a heat exchanger, positioned between absorber and desorber, which heat exchanger is equipped to exchange heat between the CO 2 -depleted solvent stream originating from the desorber and the CO2-rich solvent stream originating from the absorber.
- the installation is provided with a filtration unit to which at least a portion of the CO2-depleted solvent stream originating from the desorber is fed and optionally with an ion exchanger to which at least a portion of the CO2-depleted solvent stream originating from the desorber downstream of the filtration unit is fed.
- the installation can be provided with a combustion installation provided with a feed for oxygen-rich flue gas, a feed for a carbon-containing gas and a discharge for oxygen-depleted flue gas.
- Figure 1 is a process diagram of the method according to the present invention
- Figure 2 is a process diagram of the method according to Example 1;
- Figure 3 is a process diagram of the method according to Example 2.
- Figure 4 is a process diagram of the method according to Example 3.
- the incoming flue gas is, if necessary, cooled in the flue gas water cooler (G) and pumped through the flue gas compressor (I) to the absorber (A).
- a knock-out drum (H) can also be positioned downstream of the cooler (G) in order to separate off mist droplets (that have formed).
- the CO 2 present is absorbed by the circulating solvent in the absorber (A).
- NO x and SO2 are also virtually completely absorbed.
- the two latter acid gases will not be desorbed in the stripper, but will form anions with the solvent. These anions lead to the formation of heat stable salts.
- An outgoing CO 2 -depleted gas stream (3) issues from the absorber (A).
- This gas stream in general has a residual CO2 content of only 0.5 % (V/V). Because this stream contains more water (vapour) than the incoming gas stream, make-up water (2) is metered in.
- the CO2-rich solvent stream leaves the absorber via (4) and is fed via heat exchanger (J) to desorber (B). In the heat exchanger (J) the CO 2 -rich solvent stream (4) is heated by means of CO2-depleted solvent stream (5).
- the absorbed CO2 is stripped from the absorbent in the desorber or stripper (B).
- the requisite energy is supplied to the stripper (B) by means of reboiler (C).
- the gas that leaves the stripper (B) via the top contains some water vapour and solvent.
- These components are removed by cooling the gas stream in a condenser (D) and then separating off the condensed droplets in the distillate drum (E).
- the collected liquid is returned to desorber (B).
- the CO2 gas (7) now obtained is of such quality that it can be used as such as food grade and high purity CO2. By cooling to a lower temperature in the condenser (D) it is also possible to remove all of the water.
- the CO2-depleted bottom stream (8) from the desorber (B) is returned via heat exchanger (J) and cooler (F) to absorber (A).
- degradation products of the solvent and anions formed are removed from the CO2-depleted absorbent stream (5) that leaves the desorber, optionally after heat exchange has taken place in a heat exchanger (J) and the stream has been cooled in cooler (F).
- Filtration unit (K) consists, successively, of a first mechanical filter, an active carbon filter and a second mechanical filter.
- the first mechanical filter removes the components that could contaminate the active carbon filter.
- the active carbon filter binds all organic degradation products.
- the second mechanical filter prevents carbon that has been flushed out from passing into downstream equipment.
- the filtered solvent is returned to the system.
- An ion exchanger (L) is installed to prevent accumulation of heat stable salts.
- a portion of the stream from the filtration step (K) is fed through the ion exchanger.
- the anions, formed from NO x and SO2, present in the flue gas are removed here.
- the regenerated solvent is returned to the absorber, optionally after passing through heat exchanger (J) and cooler (F).
- a small effluent stream (9) is discharged from the ion exchanger (L).
- Example 1 Food grade/high purity CO2 from flue gas from a power station Flue gas from a power station is fed at a rate of 225,147 Nm /hour to an installation according to the invention as shown in Figure 2. The designations in this figure correspond to those in Figure 1.
- the composition of this flue gas is (in % (V/V)):
- the flue gas also contains the following components (in mg/Nm ): Component Concentration
- the temperature and the pressure of the flue gas are, respectively, 100 °C and 1.05 bara.
- the solvent used is methyldiethanolamine in combination with piperazine in water.
- the methyldiethanolamine concentration is 40 wt %.
- Overhead condenser condensate gas (in) 96 1.1 gas (out) 35 1.05 16490
- the pure CO2 gas obtained has the following composition:
- This purity of the CO2 is such that it can be used without any problem in the food industry.
- a gas that contains 99.993 % (V/V) CO2 can be obtained by removing the water from this CO2.
- CO2 gas having the same composition as in Example 1 is produced in the same way from flue gas, except that a process diagram according to Figure 3 is used. This means that, compared with Figure 2, a heat exchanger (J), a filter unit (K) and an ion exchanger (L) are additionally used.
- Overhead condenser condensate gas (in) 96 1.1 gas (out) 35 1.05 16490
- Example 2 corresponds to Example 2, except that pre-combustion of the residual oxygen in the flue gas is carried out with the aid of natural gas in combustion unit (X) (see Figure 4). h order to produce the same quantity of CO2 as in Examples 1 and 2 97961 Nm /h flue gas is required instead of 225147 Nm /h. In addition, 4703 Nm /h natural gas is required for combustion of the residual oxygen in the flue gas. The other streams are comparable to those in Example 2.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Analytical Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Biomedical Technology (AREA)
- Environmental & Geological Engineering (AREA)
- Treating Waste Gases (AREA)
- Gas Separation By Absorption (AREA)
Abstract
L'invention porte sur un procédé de récupération du CO2 très pur présent dans des fumées comportant les étapes suivantes: a) absorption du CO2 des fumées par un solvant contenu dans un absorbeur, tandis qu'un courant gazeux appauvri en CO2 et un flux de solvant enrichi en CO2 quittent l'absorbeur et b) désorption du CO2 absorbé dans un désorbeur tandis qu'un courant gazeux enrichi en CO2 et un flux de solvant appauvri en CO2 quittent le désorbeur. Le solvant utilisé est une solution aqueuse contenant une alcanolamine et un activateur. On utilise de préférence une combinaison de méthyldiéthanolamine et de pipérazine. On récupère ainsi un CO2 très pur dit de haute pureté ou de niveau alimentaire.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL1015827 | 2000-07-27 | ||
NL1015827A NL1015827C2 (nl) | 2000-07-27 | 2000-07-27 | Winning van zuiver CO2 uit rookgassen. |
PCT/NL2001/000580 WO2002009849A2 (fr) | 2000-07-27 | 2001-07-27 | Recuperation de co2 tres pur dans des fumees |
Publications (1)
Publication Number | Publication Date |
---|---|
EP1303344A2 true EP1303344A2 (fr) | 2003-04-23 |
Family
ID=19771818
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP01967856A Withdrawn EP1303344A2 (fr) | 2000-07-27 | 2001-07-27 | Recuperation de co 2? tres pur dans des fumees |
Country Status (4)
Country | Link |
---|---|
EP (1) | EP1303344A2 (fr) |
AU (1) | AU2001288142A1 (fr) |
NL (1) | NL1015827C2 (fr) |
WO (1) | WO2002009849A2 (fr) |
Families Citing this family (36)
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DE10139453A1 (de) * | 2001-08-10 | 2003-02-20 | Basf Ag | Verfahren und Absorptionsmittel zur Entfernung saurer Gase aus Fluiden |
NZ514666A (en) * | 2001-10-08 | 2003-01-31 | Canterprise Ltd | Apparatus for continuous carbon dioxide absorption comprising a reactor containing a carbon dioxide absorbent liquid recycled via a regenerator |
US7056482B2 (en) * | 2003-06-12 | 2006-06-06 | Cansolv Technologies Inc. | Method for recovery of CO2 from gas streams |
DE102004011428A1 (de) * | 2004-03-09 | 2005-09-29 | Basf Ag | Verfahren zum Entfernen von Kohlendioxid aus Rauchgasen |
DE102004011429A1 (de) * | 2004-03-09 | 2005-09-29 | Basf Ag | Verfahren zum Entfernen von Kohlendioxid aus Gasströmen mit niedrigen Kohlendioxid-Partialdrücken |
DE102005050385A1 (de) | 2005-10-20 | 2007-04-26 | Basf Ag | Absorptionsmittel und Verfahren zum Entfernen von Kohlendioxid aus Gasströmen |
PE20071048A1 (es) | 2005-12-12 | 2007-10-18 | Basf Ag | Proceso para la recuperacion de dioxido de carbono |
AU2007253430B2 (en) | 2006-05-18 | 2011-03-10 | Basf Se | Carbon dioxide absorbent requiring less regeneration energy |
HUE029307T2 (en) * | 2006-05-19 | 2017-02-28 | Basf Se | Pre-mix to produce an absorption agent for removing acid gases from liquid streams |
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 |
US7887620B2 (en) | 2006-06-13 | 2011-02-15 | Basf Se | Removal of carbon dioxide from flue gases |
US7601315B2 (en) * | 2006-12-28 | 2009-10-13 | Cansolv Technologies Inc. | Process for the recovery of carbon dioxide from a gas stream |
EP2217353B1 (fr) | 2007-11-15 | 2017-01-25 | Basf Se | Procédé pour éliminer du dioxyde de carbone de courants de fluides, en particulier de gaz de combustion |
US7862788B2 (en) | 2007-12-05 | 2011-01-04 | Alstom Technology Ltd | Promoter enhanced chilled ammonia based system and method for removal of CO2 from flue gas stream |
US8192530B2 (en) | 2007-12-13 | 2012-06-05 | Alstom Technology Ltd | System and method for regeneration of an absorbent solution |
JP5072627B2 (ja) | 2008-02-01 | 2012-11-14 | 三菱重工業株式会社 | Co2回収装置及びろ過膜装置の洗浄方法 |
US8318117B2 (en) | 2008-06-23 | 2012-11-27 | Basf Se | Absorption medium and method for removing sour gases from fluid streams, in particular from flue gases |
US8404027B2 (en) | 2008-11-04 | 2013-03-26 | Alstom Technology Ltd | Reabsorber for ammonia stripper offgas |
JP5173941B2 (ja) * | 2009-06-04 | 2013-04-03 | 三菱重工業株式会社 | Co2回収装置 |
EP2283911A1 (fr) * | 2009-08-11 | 2011-02-16 | Shell Internationale Research Maatschappij B.V. | Procédé pour l'élimination de CO2 et/ou de H2S d'un gaz comprenant du CO2 et/ou du H2S |
US20120216678A1 (en) * | 2009-08-11 | 2012-08-30 | Frank Haiko Geuzebroek | Absorbent composition and process for removing co2 and/or h2s from a gas comprising co2 and/or h2s |
EP2322265A1 (fr) | 2009-11-12 | 2011-05-18 | Alstom Technology Ltd | Système de traitement de gaz de fumée |
US8728209B2 (en) | 2010-09-13 | 2014-05-20 | Alstom Technology Ltd | Method and system for reducing energy requirements of a CO2 capture system |
US9133407B2 (en) | 2011-02-25 | 2015-09-15 | Alstom Technology Ltd | Systems and processes for removing volatile degradation products produced in gas purification |
JP5659084B2 (ja) * | 2011-05-30 | 2015-01-28 | 株式会社東芝 | 酸性ガス吸収剤、酸性ガス除去方法および酸性ガス除去装置 |
US8864878B2 (en) | 2011-09-23 | 2014-10-21 | Alstom Technology Ltd | Heat integration of a cement manufacturing plant with an absorption based carbon dioxide capture process |
US8911538B2 (en) | 2011-12-22 | 2014-12-16 | Alstom Technology Ltd | Method and system for treating an effluent stream generated by a carbon capture system |
US9162177B2 (en) | 2012-01-25 | 2015-10-20 | Alstom Technology Ltd | Ammonia capturing by CO2 product liquid in water wash liquid |
US9028654B2 (en) | 2012-02-29 | 2015-05-12 | Alstom Technology Ltd | Method of treatment of amine waste water and a system for accomplishing the same |
US8864879B2 (en) | 2012-03-30 | 2014-10-21 | Jalal Askander | System for recovery of ammonia from lean solution in a chilled ammonia process utilizing residual flue gas |
US9101912B2 (en) | 2012-11-05 | 2015-08-11 | Alstom Technology Ltd | Method for regeneration of solid amine CO2 capture beds |
US9447996B2 (en) | 2013-01-15 | 2016-09-20 | General Electric Technology Gmbh | Carbon dioxide removal system using absorption refrigeration |
US8986640B1 (en) | 2014-01-07 | 2015-03-24 | Alstom Technology Ltd | System and method for recovering ammonia from a chilled ammonia process |
CN104645807A (zh) * | 2014-12-31 | 2015-05-27 | 中国船舶重工集团公司第七一八研究所 | 一种二氧化碳捕集设备 |
WO2017211932A1 (fr) * | 2016-06-10 | 2017-12-14 | Basf Se | Cyclohexandiamines utilisables pour l'épuration des gaz |
CA3041192A1 (fr) | 2016-11-01 | 2018-05-11 | Cansolv Technologies Inc | Procede pour la production de flux de gaz purifie |
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2551717C3 (de) * | 1975-11-18 | 1980-11-13 | Basf Ag, 6700 Ludwigshafen | und ggf. COS aus Gasen |
WO1989011327A1 (fr) * | 1988-05-24 | 1989-11-30 | Societe Nationale Elf Aquitaine (Production) | Liquide absorbant des gaz acides |
US5618506A (en) * | 1994-10-06 | 1997-04-08 | The Kansai Electric Power Co., Inc. | Process for removing carbon dioxide from gases |
-
2000
- 2000-07-27 NL NL1015827A patent/NL1015827C2/nl not_active IP Right Cessation
-
2001
- 2001-07-27 AU AU2001288142A patent/AU2001288142A1/en not_active Abandoned
- 2001-07-27 EP EP01967856A patent/EP1303344A2/fr not_active Withdrawn
- 2001-07-27 WO PCT/NL2001/000580 patent/WO2002009849A2/fr not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
NL1015827C2 (nl) | 2002-02-01 |
WO2002009849A3 (en) | 2002-04-25 |
AU2001288142A1 (en) | 2002-02-13 |
WO2002009849A2 (fr) | 2002-02-07 |
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