US20120144860A1 - Process for removing harmful substances from liquid carbon dioxide and apparatus for the performance thereof - Google Patents
Process for removing harmful substances from liquid carbon dioxide and apparatus for the performance thereof Download PDFInfo
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- US20120144860A1 US20120144860A1 US13/384,616 US201013384616A US2012144860A1 US 20120144860 A1 US20120144860 A1 US 20120144860A1 US 201013384616 A US201013384616 A US 201013384616A US 2012144860 A1 US2012144860 A1 US 2012144860A1
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- carbon dioxide
- substance
- harmful substances
- harmful substance
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- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 title claims abstract description 94
- 239000000126 substance Substances 0.000 title claims abstract description 55
- 229910002092 carbon dioxide Inorganic materials 0.000 title claims abstract description 50
- 239000001569 carbon dioxide Substances 0.000 title claims abstract description 48
- 238000000034 method Methods 0.000 title claims abstract description 30
- 239000007788 liquid Substances 0.000 title claims abstract description 22
- 239000007789 gas Substances 0.000 claims abstract description 18
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 9
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract description 8
- 230000000274 adsorptive effect Effects 0.000 claims abstract description 6
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 claims abstract description 6
- 229910052753 mercury Inorganic materials 0.000 claims abstract description 6
- 238000009833 condensation Methods 0.000 claims abstract description 5
- 230000005494 condensation Effects 0.000 claims abstract description 5
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims abstract description 4
- 229910002091 carbon monoxide Inorganic materials 0.000 claims abstract description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 4
- 239000001257 hydrogen Substances 0.000 claims abstract description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 4
- 229910052756 noble gas Inorganic materials 0.000 claims abstract description 4
- 150000002731 mercury compounds Chemical class 0.000 claims abstract description 3
- 238000000926 separation method Methods 0.000 claims description 13
- 239000003463 adsorbent Substances 0.000 claims description 7
- 239000000203 mixture Substances 0.000 claims description 7
- 229910052717 sulfur Inorganic materials 0.000 claims description 7
- 239000011593 sulfur Substances 0.000 claims description 7
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 6
- 230000008929 regeneration Effects 0.000 claims description 5
- 238000011069 regeneration method Methods 0.000 claims description 5
- 150000001875 compounds Chemical class 0.000 claims description 4
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 3
- 229920000642 polymer Polymers 0.000 claims description 3
- 239000010457 zeolite Substances 0.000 claims description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 2
- 239000000741 silica gel Substances 0.000 claims description 2
- 229910002027 silica gel Inorganic materials 0.000 claims description 2
- 229910021536 Zeolite Inorganic materials 0.000 claims 2
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 2
- 150000003464 sulfur compounds Chemical class 0.000 claims 1
- 150000002431 hydrogen Chemical class 0.000 abstract description 2
- 150000002835 noble gases Chemical class 0.000 abstract description 2
- 239000005864 Sulphur Substances 0.000 abstract 1
- 239000007791 liquid phase Substances 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 239000006096 absorbing agent Substances 0.000 description 4
- JJWKPURADFRFRB-UHFFFAOYSA-N carbonyl sulfide Chemical compound O=C=S JJWKPURADFRFRB-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000001179 sorption measurement Methods 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 238000005201 scrubbing Methods 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 230000018109 developmental process Effects 0.000 description 2
- 238000005265 energy consumption Methods 0.000 description 2
- 239000002803 fossil fuel Substances 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 239000005431 greenhouse gas Substances 0.000 description 1
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 1
- CRVGTESFCCXCTH-UHFFFAOYSA-N methyl diethanolamine Chemical compound OCCN(C)CCO CRVGTESFCCXCTH-UHFFFAOYSA-N 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000004088 simulation Methods 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 239000002912 waste gas Substances 0.000 description 1
Images
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
- B01D53/002—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 condensation
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D17/00—Separation of liquids, not provided for elsewhere, e.g. by thermal diffusion
- B01D17/02—Separation of non-miscible liquids
- B01D17/0202—Separation of non-miscible liquids by ab- or adsorption
-
- 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
- B01D53/02—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 adsorption, e.g. preparative gas chromatography
- B01D53/04—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 adsorption, e.g. preparative gas chromatography with stationary adsorbents
-
- 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
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2256/00—Main component in the product gas stream after treatment
- B01D2256/22—Carbon dioxide
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2257/00—Components to be removed
- B01D2257/30—Sulfur compounds
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2257/00—Components to be removed
- B01D2257/60—Heavy metals or heavy metal compounds
- B01D2257/602—Mercury or mercury compounds
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2259/00—Type of treatment
- B01D2259/40—Further details for adsorption processes and devices
- B01D2259/40083—Regeneration of adsorbents in processes other than pressure or temperature swing adsorption
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2259/00—Type of treatment
- B01D2259/40—Further details for adsorption processes and devices
- B01D2259/416—Further details for adsorption processes and devices involving cryogenic temperature treatment
-
- 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
Definitions
- the invention relates to a process and to an apparatus for separating harmful substances from a carbon dioxide stream.
- Compounds of sulfur or mercury are examples of harmful substances.
- the latest power station concepts include general conditions which in each case provide the most advanced techniques for separating harmful substances according to the current prior art.
- liquid absorber media are for example aqueous alkanolamine solutions, specifically aqueous methyl diethanolamine, or for example cold methanol, employed in the Rectisol process. Such processes using liquid absorber media are known and established in various technologies.
- the regeneration of absorber media is accomplished by means of distillation, with which a substantial degree of energy consumption is associated.
- the object of the invention is to describe an energy-saving option for removing harmful substances in power stations which are substantially fired by fossil fuels. It is furthermore intended to disclose an easy-to-use apparatus for performing the process.
- the invention is based on the fact that in the case of a gas mixture which in large part consists of carbon dioxide CO 2 and includes proportions of valuable gases and harmful substances, particularly in the case of condensation of the carbon dioxide, the harmful substances preferably accumulate in the liquid carbon dioxide.
- This knowledge is exploited to the effect that the separation of the harmful substances from the liquid phase of the carbon dioxide takes place at low temperatures through the use of adsorber materials/adsorbents, preferably solid adsorber materials.
- the energy balance associated with separating harmful substances at low temperatures turns out to be positive, in other words the overall energy requirement is less.
- the separation of the harmful substances from the liquid phase can take place at low temperatures very advantageously by means of adsorber materials because the materials employed here have large surface areas which are available for the absorption of the harmful substances.
- the process pressure must in principle lie above the triple point of carbon dioxide in accordance with the temperature/pressure diagram. It is thus at least 5 bar.
- a temperature range which can likewise be used for the process temperature begins at ⁇ 5° C. and extends toward lower temperatures.
- the use of the process for separating harmful substances from a gas mixture which substantially consists of carbon dioxide can be implemented particularly advantageously in so-called zero-carbon dioxide power stations.
- the separation of the carbon dioxide can be carried out cryogenically.
- the carbon dioxide is brought to a low temperature, liquefied and separated out.
- the liquid phase is very well suited for the adsorptive separation of harmful substances because the latter by preference accumulate in the liquid carbon dioxide.
- low temperatures promote adsorption, which means for example that a gas scrubbing stage as provided in the prior art is no longer necessary.
- the use of fixed-bed adsorbers for the adsorption of harmful substances is advantageous because solids having a large surface area are employed here. These are in particular alumina (aluminum oxide), activated carbon, silica gel, zeolites or polymers having a large surface area.
- FIG. 1 schematically illustrates a fixed-bed adsorber through which liquid carbon dioxide containing harmful substances is fed, the harmful substances being adsorbed in the fixed-bed adsorber.
- FIG. 2 illustrates adsorbers connected in parallel which can be switched over individually or in groups between the adsorption and regeneration operating states by means of corresponding valves.
- the adsorption of harmful substances is carried out in fixed-bed adsorbers, such as are illustrated in FIGS. 1 and 2 .
- fixed-bed adsorbers such as are illustrated in FIGS. 1 and 2 .
- An arrangement of three fixed-bed adsorbers is illustrated in FIG. 2 . Analogous configurations for two or more than three adsorbers are possible.
- a process according to the invention can be excellently combined with a power station concept which already provides cryogenic carbon dioxide separation.
- the temperature range for operating the process can lie between ⁇ 5° C. and ⁇ 70° C.
- the lower temperature limit lies in the region of the solidification of carbon dioxide from the liquid phase, which means that solids can block the process.
- the energy balance of the entire process reveals that temperatures of ⁇ 30° C. and lower are advantageous for the separation of harmful substances.
- the valuable gases such as hydrogen, carbon monoxide, nitrogen or noble gases which may be present in the gaseous or liquid stream in the process are not adsorbed in the course of the described process approach.
- Harmful substances such as mercury, sulfur or their compounds, which are to be found substantially in the liquid carbon dioxide stream, accumulate on the surface in the fixed-bed adsorbers, in other words are adsorbed by the adsorbents, and are thus retained in the fixed-bed adsorbers.
- a further harmful substance which can be separated out in this manner is carbonyl sulfide COS.
- FIG. 1 shows a fixed-bed adsorber 1 into which a liquid carbon dioxide stream 2 containing harmful substances is introduced.
- a liquid carbon dioxide stream 3 free of harmful substances emerges at the outlet of the fixed-bed adsorber 1 .
- FIG. 2 shows three fixed-bed adsorbers 1 connected in parallel.
- the liquid carbon dioxide stream 2 is supplied at the top, harmful substances are captured in the fixed-bed adsorbers 1 , and the liquid carbon dioxide stream 3 free of harmful substances can be removed at the bottom.
- Individual fixed-bed adsorbers 1 can be switched over in each case for regeneration purposes 4 .
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Analytical Chemistry (AREA)
- Thermal Sciences (AREA)
- Physics & Mathematics (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
- Separation Of Gases By Adsorption (AREA)
- Carbon And Carbon Compounds (AREA)
- Treating Waste Gases (AREA)
- Gas Separation By Absorption (AREA)
Abstract
A process for removing harmful substances from a gas steam which includes carbon dioxide and substances of value, such as at least one of the gases hydrogen H2 carbon monoxide CO, nitrogen N2 or noble gases, and harmful substances such as a substance from the group of mercury, sulphur, mercury compounds or sulphur compounds, wherein a carbon dioxide condensation is performed in order to obtain liquid carbon dioxide, adsorptive removal of the harmful substances from the condensed carbon dioxide is performed to remove the harmful substances from the carbon dioxide. A process temperature of less than −30° C. but great than −70° C. is maintained.
Description
- This application is the US National Stage of International Application No. PCT/EP2010/060335, filed Jul. 16, 2010 and claims the benefit thereof. The International Application claims the benefits of German application No. 10 2009 035 389.5 DE filed Jul. 30, 2009. All of the applications are incorporated by reference herein in their entirety.
- The invention relates to a process and to an apparatus for separating harmful substances from a carbon dioxide stream. Compounds of sulfur or mercury are examples of harmful substances.
- On account of the so-called greenhouse effect and the global temperature rise associated therewith, the emission of greenhouse gases into the atmosphere is subject to increasing criticism. A considerable proportion of the greenhouse effect is attributed to carbon dioxide CO2 which is produced during the combustion of fossil fuels.
- There is currently a consensus across society that separating out carbon dioxide from power station waste gases may counteract an increase in the greenhouse effect. For this reason, corresponding further developments are directed at making possible plants having low levels of carbon dioxide emissions or even none at all. Accordingly, the latest concepts for power stations having low levels of carbon dioxide emissions or which are free of carbon dioxide emissions are at the development stage. All of these concepts pursue the common objective of separating the carbon dioxide as completely as possible and at a high level of purity with minimal energy consumption.
- Here the focus is on the separation of the carbon dioxide in the first instance. In addition, however, further undesirable substances are present which occur depending on the type of fuel and which need to be removed. Sulfur, mercury or their compounds are the most commonly encountered substances in terms of quantity in this context.
- The latest power station concepts include general conditions which in each case provide the most advanced techniques for separating harmful substances according to the current prior art.
- According to the prior art, harmful substances which accumulate in power stations, such as sulfur or mercury compounds, are removed directly from the gas phase. Thus, hydrogen sulfide, for example, is separated by means of gas scrubbing. This entails routing the gas stream through an absorber in which a liquid medium absorbs the harmful substances. Liquid absorber media are for example aqueous alkanolamine solutions, specifically aqueous methyl diethanolamine, or for example cold methanol, employed in the Rectisol process. Such processes using liquid absorber media are known and established in various technologies.
- Disadvantages in the prior art consist primarily in the fact that gas scrubbing processes involve an increased energy requirement because they may be associated with process steps such as compression and/or cooling.
- The regeneration of absorber media is accomplished by means of distillation, with which a substantial degree of energy consumption is associated.
- Furthermore, processes of said type are relatively complicated in terms of infrastructure and setup, which has disadvantageous implications in relation to process implementation and investment costs.
- The object of the invention is to describe an energy-saving option for removing harmful substances in power stations which are substantially fired by fossil fuels. It is furthermore intended to disclose an easy-to-use apparatus for performing the process.
- The invention is based on the fact that in the case of a gas mixture which in large part consists of carbon dioxide CO2 and includes proportions of valuable gases and harmful substances, particularly in the case of condensation of the carbon dioxide, the harmful substances preferably accumulate in the liquid carbon dioxide. This knowledge is exploited to the effect that the separation of the harmful substances from the liquid phase of the carbon dioxide takes place at low temperatures through the use of adsorber materials/adsorbents, preferably solid adsorber materials. In this case it is particularly advantageous that the energy balance associated with separating harmful substances at low temperatures turns out to be positive, in other words the overall energy requirement is less.
- The separation of the harmful substances from the liquid phase can take place at low temperatures very advantageously by means of adsorber materials because the materials employed here have large surface areas which are available for the absorption of the harmful substances.
- If the process for separating harmful substances from a gas stream consisting substantially of carbon dioxide is combined with a process in which carbon dioxide is already present in liquid form, synergistic effects in the overall energy balance can thereby be achieved.
- It is particularly advantageous to set and maintain the process temperature at less than −30° C. It is not beneficial to use temperatures below −70° C. because carbon dioxide exists in the solid phase at such low temperatures.
- The process pressure must in principle lie above the triple point of carbon dioxide in accordance with the temperature/pressure diagram. It is thus at least 5 bar. A temperature range which can likewise be used for the process temperature begins at −5° C. and extends toward lower temperatures.
- The use of the process for separating harmful substances from a gas mixture which substantially consists of carbon dioxide can be implemented particularly advantageously in so-called zero-carbon dioxide power stations. In said power stations the separation of the carbon dioxide can be carried out cryogenically. With this approach the carbon dioxide is brought to a low temperature, liquefied and separated out. The liquid phase is very well suited for the adsorptive separation of harmful substances because the latter by preference accumulate in the liquid carbon dioxide. Furthermore, low temperatures promote adsorption, which means for example that a gas scrubbing stage as provided in the prior art is no longer necessary. The use of fixed-bed adsorbers for the adsorption of harmful substances is advantageous because solids having a large surface area are employed here. These are in particular alumina (aluminum oxide), activated carbon, silica gel, zeolites or polymers having a large surface area.
- Since the surface area of the adsorbents becomes populated with harmful substances in the course of the process, a periodic regeneration of individual fixed-bed adsorbers is advantageously provided.
- Exemplary embodiments will be described in the following with reference to schematic accompanying figures, in which specifically:
-
FIG. 1 schematically illustrates a fixed-bed adsorber through which liquid carbon dioxide containing harmful substances is fed, the harmful substances being adsorbed in the fixed-bed adsorber. -
FIG. 2 illustrates adsorbers connected in parallel which can be switched over individually or in groups between the adsorption and regeneration operating states by means of corresponding valves. - The adsorption of harmful substances is carried out in fixed-bed adsorbers, such as are illustrated in
FIGS. 1 and 2 . After a certain period of use it is necessary to regenerate the adsorbents. This is effected by means of a reduction in pressure, an increase in temperature, or by feeding through a gas or vapor, or by a combination thereof. For this reason there exist a plurality of adsorbers which are in operation or can be regenerated on an alternating basis. An arrangement of three fixed-bed adsorbers is illustrated inFIG. 2 . Analogous configurations for two or more than three adsorbers are possible. - During the carbon dioxide condensation a substantial accumulation of harmful substances contained in a gas mixture occurs automatically in the liquid carbon dioxide. It has been possible to demonstrate this with the aid of simulation calculations taking as example hydrogen sulfide H2S and also carbonyl sulfide COS. The harmful substances can subsequently be separated out from the liquid phase at low temperatures by means of adsorber materials.
- The energy-saving separation of the harmful substances at lower temperatures in the overall concept is advantageous. A process according to the invention can be excellently combined with a power station concept which already provides cryogenic carbon dioxide separation.
- The temperature range for operating the process can lie between −5° C. and −70° C. The lower temperature limit lies in the region of the solidification of carbon dioxide from the liquid phase, which means that solids can block the process. As a general rule it is necessary to ensure that the fixed-bed adsorbers are kept open for the liquid reaction stream. However, the energy balance of the entire process reveals that temperatures of −30° C. and lower are advantageous for the separation of harmful substances.
- The valuable gases such as hydrogen, carbon monoxide, nitrogen or noble gases which may be present in the gaseous or liquid stream in the process are not adsorbed in the course of the described process approach. Harmful substances such as mercury, sulfur or their compounds, which are to be found substantially in the liquid carbon dioxide stream, accumulate on the surface in the fixed-bed adsorbers, in other words are adsorbed by the adsorbents, and are thus retained in the fixed-bed adsorbers. A further harmful substance which can be separated out in this manner is carbonyl sulfide COS.
-
FIG. 1 shows a fixed-bed adsorber 1 into which a liquidcarbon dioxide stream 2 containing harmful substances is introduced. A liquid carbon dioxide stream 3 free of harmful substances emerges at the outlet of the fixed-bed adsorber 1. -
FIG. 2 shows three fixed-bed adsorbers 1 connected in parallel. The liquidcarbon dioxide stream 2 is supplied at the top, harmful substances are captured in the fixed-bed adsorbers 1, and the liquid carbon dioxide stream 3 free of harmful substances can be removed at the bottom. Individual fixed-bed adsorbers 1 can be switched over in each case forregeneration purposes 4. - While a direct catalytic conversion may be associated with a favorable state of equilibrium on account of the low temperatures, it does however exhibit very unfavorable kinetics. Very large quantities of catalysts would be required, which would probably become very rapidly deactivated due to the presence of sulfur.
Claims (11)
1-8. (canceled)
9. A process for separating a harmful substance from a gas mixture which essentially consists of carbon dioxide as well as a recyclable substance, comprising:
carrying out a carbon dioxide condensation in order to produce and to separate liquid carbon dioxide;
carrying out an adsorptive separation of the harmful substance from the liquid carbon dioxide in order to remove the harmful substance from the liquid carbon dioxide; and
setting a process temperature in a range from −30° C. to −70° C.
10. The process as claimed in claim 9 , wherein the recyclable substance contained in the gas mixture is selected from the group consisting of hydrogen, carbon monoxide, nitrogen, and a noble gas.
11. The process as claimed in claim 9 , wherein the harmful substance contained in the gas mixture is selected from the group consisting of sulfur, mercury, sulfur compounds and mercury compounds.
12. The process as claimed in claim 9 , wherein that at least one substance from a group of substances comprising activated carbon, zeolite, silica gel, alumina or at least one polymer having a large surface area is selected as an adsorbent for the adsorptive separation of the harmful substance.
13. The process as claimed in claim 9 , wherein the separation of at least one harmful substance from cryogenic carbon dioxide takes place in low- or zero-carbon dioxide power stations.
14. An apparatus for separating a harmful substance from a gas mixture which essentially consists of carbon dioxide as well as a recyclable substance, comprising:
a carbon dioxide condensation unit for producing liquid carbon dioxide; and
a fixed-bed adsorber for the adsorptive separation of the harmful substance from liquid carbon dioxide for the purpose of removing the harmful substances therefrom, and
wherein the operating temperature of the apparatus lies in a range from −70° C. to −30° C.
15. The apparatus as claimed in claim 14 , wherein for the purpose of the adsorptive separation, the fixed-bed adsorber includes at least one adsorbent selected from the group consisting of activated carbon, zeolite, alumina and a polymer having a large surface area.
16. The apparatus as claimed in claim 14 ,
wherein a plurality of fixed-bed adsorbers are present, and
wherein the plurality of fixed-bed adsorbers may be connected in parallel in groups, such that adsorbers or groups of adsorbers may be switched over to allow regeneration of the adsorbents.
17. The apparatus as claimed in claim 14 , wherein the recyclable substance is selected from the group consisting of hydrogen, carbon monoxide, nitrogen, and a noble gas.
18. The apparatus as claimed in claim 14 , wherein the harmful substance is selected from the group consisting of mercury, sulfur, and compounds thereof.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102009035389.5 | 2009-07-30 | ||
| DE102009035389A DE102009035389A1 (en) | 2009-07-30 | 2009-07-30 | Process for pollutant removal from carbon dioxide and apparatus for carrying it out |
| PCT/EP2010/060335 WO2011012470A1 (en) | 2009-07-30 | 2010-07-16 | Process for removing harmful substances from liquid carbon dioxide and apparatus for performance thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US20120144860A1 true US20120144860A1 (en) | 2012-06-14 |
Family
ID=42628433
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US13/384,616 Abandoned US20120144860A1 (en) | 2009-07-30 | 2010-07-16 | Process for removing harmful substances from liquid carbon dioxide and apparatus for the performance thereof |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US20120144860A1 (en) |
| EP (1) | EP2459293A1 (en) |
| KR (1) | KR20120055576A (en) |
| CN (1) | CN102470287B (en) |
| AU (1) | AU2010277760B2 (en) |
| BR (1) | BR112012001719A2 (en) |
| CA (1) | CA2769495C (en) |
| DE (1) | DE102009035389A1 (en) |
| RU (1) | RU2551510C2 (en) |
| WO (1) | WO2011012470A1 (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9458022B2 (en) | 2014-03-28 | 2016-10-04 | L'Air Liquide Société Anonyme Pour L'Étude Et L'Exploitation Des Procedes Georges Claude | Process and apparatus for separating NO2 from a CO2 and NO2—containing fluid |
| US11135542B2 (en) | 2016-10-28 | 2021-10-05 | Uop Llc | Processes and apparatuses for removing contaminants from hydrogen streams |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102010006102A1 (en) | 2010-01-28 | 2011-08-18 | Siemens Aktiengesellschaft, 80333 | Process for the separation of purified value gas from a gas mixture, and apparatus for carrying out this process |
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- 2010-07-16 BR BR112012001719A patent/BR112012001719A2/en not_active Application Discontinuation
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Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9458022B2 (en) | 2014-03-28 | 2016-10-04 | L'Air Liquide Société Anonyme Pour L'Étude Et L'Exploitation Des Procedes Georges Claude | Process and apparatus for separating NO2 from a CO2 and NO2—containing fluid |
| US9816755B2 (en) | 2014-03-28 | 2017-11-14 | L'Air Liquide Société Anonyme Pour L'Étude Et L'Exploitation Des Procedes Georges Claude | Process and apparatus for separating NO2 from a CO2 and NO2-containing fluid |
| US11135542B2 (en) | 2016-10-28 | 2021-10-05 | Uop Llc | Processes and apparatuses for removing contaminants from hydrogen streams |
Also Published As
| Publication number | Publication date |
|---|---|
| CA2769495A1 (en) | 2011-02-03 |
| WO2011012470A1 (en) | 2011-02-03 |
| CN102470287B (en) | 2015-09-30 |
| DE102009035389A1 (en) | 2011-02-03 |
| BR112012001719A2 (en) | 2016-04-12 |
| CA2769495C (en) | 2018-05-22 |
| CN102470287A (en) | 2012-05-23 |
| RU2551510C2 (en) | 2015-05-27 |
| AU2010277760A1 (en) | 2012-02-02 |
| AU2010277760B2 (en) | 2015-02-19 |
| KR20120055576A (en) | 2012-05-31 |
| RU2012107387A (en) | 2013-09-10 |
| EP2459293A1 (en) | 2012-06-06 |
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