[go: up one dir, main page]

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 PDF

Info

Publication number
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
Authority
US
United States
Prior art keywords
carbon dioxide
substance
harmful substances
harmful substance
group
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.)
Abandoned
Application number
US13/384,616
Inventor
Manfred Baldauf
Carsten Graeber
Marc Hanebuth
Gerhard Zimmermann
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Siemens AG
Original Assignee
Siemens AG
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Siemens AG filed Critical Siemens AG
Assigned to SIEMENS AKTIENGESELLSCHAFT reassignment SIEMENS AKTIENGESELLSCHAFT ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: GRAEBER, CARSTEN, ZIMMERMANN, GERHARD, HANEBUTH, MARC, BALDAUF, MANFRED
Publication of US20120144860A1 publication Critical patent/US20120144860A1/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation 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
    • B01D53/002Separation 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
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D17/00Separation of liquids, not provided for elsewhere, e.g. by thermal diffusion
    • B01D17/02Separation of non-miscible liquids
    • B01D17/0202Separation of non-miscible liquids by ab- or adsorption
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation 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
    • B01D53/02Separation 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
    • B01D53/04Separation 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
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B32/00Carbon; Compounds thereof
    • C01B32/50Carbon dioxide
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2256/00Main component in the product gas stream after treatment
    • B01D2256/22Carbon dioxide
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2257/00Components to be removed
    • B01D2257/30Sulfur compounds
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2257/00Components to be removed
    • B01D2257/60Heavy metals or heavy metal compounds
    • B01D2257/602Mercury or mercury compounds
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2259/00Type of treatment
    • B01D2259/40Further details for adsorption processes and devices
    • B01D2259/40083Regeneration of adsorbents in processes other than pressure or temperature swing adsorption
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2259/00Type of treatment
    • B01D2259/40Further details for adsorption processes and devices
    • B01D2259/416Further details for adsorption processes and devices involving cryogenic temperature treatment
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02CCAPTURE, STORAGE, SEQUESTRATION OR DISPOSAL OF GREENHOUSE GASES [GHG]
    • Y02C20/00Capture or disposal of greenhouse gases
    • Y02C20/40Capture 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 .

Landscapes

  • 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

    CROSS REFERENCE TO RELATED APPLICATIONS
  • 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.
  • FIELD OF INVENTION
  • 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.
  • BACKGROUND OF INVENTION
  • 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.
  • SUMMARY OF INVENTION
  • 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.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • 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.
  • DETAILED DESCRIPTION OF INVENTION
  • 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 in FIG. 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 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.
  • 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.
US13/384,616 2009-07-30 2010-07-16 Process for removing harmful substances from liquid carbon dioxide and apparatus for the performance thereof Abandoned US20120144860A1 (en)

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)

* Cited by examiner, † Cited by third party
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)

* Cited by examiner, † Cited by third party
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

Citations (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2039330A (en) * 1930-07-08 1936-05-05 Ralph H Mckee Purification of carbon dioxide
US3001373A (en) * 1958-04-11 1961-09-26 Texaco Inc Separation of carbon dioxide from gaseous mixtures
US3074245A (en) * 1957-07-18 1963-01-22 Linde Eismasch Ag Process for the selective removal of carbon dioxide and hydrogen sulfide from gaseous mixtures containing the same
US3421984A (en) * 1967-05-02 1969-01-14 Susquehanna Corp Purification of fluids by selective adsorption of an impure side stream from a distillation with adsorber regeneration
US4052176A (en) * 1975-09-29 1977-10-04 Texaco Inc. Production of purified synthesis gas H2 -rich gas, and by-product CO2 -rich gas
US4144038A (en) * 1976-12-20 1979-03-13 Boc Limited Gas separation
US4270937A (en) * 1976-12-01 1981-06-02 Cng Research Company Gas separation process
US4759848A (en) * 1985-01-23 1988-07-26 Mg Industries Sterilization of cryogenic liquids by ultrafiltration
US4784672A (en) * 1987-10-08 1988-11-15 Air Products And Chemicals, Inc. Regeneration of adsorbents
US5100635A (en) * 1990-07-31 1992-03-31 The Boc Group, Inc. Carbon dioxide production from combustion exhaust gases with nitrogen and argon by-product recovery
US5271760A (en) * 1993-03-01 1993-12-21 Uop Recovery of liquid mercury from process streams
US5450728A (en) * 1993-11-30 1995-09-19 Air Products And Chemicals, Inc. Recovery of volatile organic compounds from gas streams
US5837032A (en) * 1991-01-30 1998-11-17 The Cynara Company Gas separations utilizing glassy polymer membranes at sub-ambient temperatures
US5925326A (en) * 1995-08-23 1999-07-20 The Boc Group, Inc. Process for the production of high purity carbon dioxide
US6119480A (en) * 1998-01-23 2000-09-19 L'air Liquide, Societe Anonyme Pour L'etude Et L'exploitation Des Procedes Georges Claude Plant and method for liquid-phase filtration of a cryogenic fluid
US6511528B1 (en) * 1999-03-26 2003-01-28 Uop Llc Purification of carbon dioxide
US20080173585A1 (en) * 2007-01-23 2008-07-24 Vincent White Purification of carbon dioxide
US20090013868A1 (en) * 2007-07-11 2009-01-15 Arthur Darde Process and apparatus for the separation of a gaseous mixture
US20090013871A1 (en) * 2007-07-11 2009-01-15 Arthur Darde Process and apparatus for the separation of a gaseous mixture
WO2009010690A2 (en) * 2007-07-13 2009-01-22 L'air Liquide Societe Anonyme Pour L'etude Et L'exploitation Des Procedes Georges Claude Method for the purification of a gas containing co2
US20090101007A1 (en) * 2004-10-08 2009-04-23 Rasmus Find Method for recovery of carbon dioxide from a gas
US7556671B2 (en) * 2005-08-08 2009-07-07 The Boc Group, Inc. System and method for purifying a gas

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2125480C1 (en) * 1994-02-15 1999-01-27 Ростовская-на-Дону государственная академия строительства Method of cleaning flue gases from gaseous contaminating components
DE69520687T2 (en) * 1994-11-09 2001-08-23 R.R. Street & Co., Inc. METHOD AND SYSTEM FOR TREATING PRESSURE LIQUID SOLVENTS FOR CLEANING SUBSTRATES
US6361696B1 (en) * 2000-01-19 2002-03-26 Aeronex, Inc. Self-regenerative process for contaminant removal from liquid and supercritical CO2 fluid streams
WO2003033114A1 (en) * 2001-10-17 2003-04-24 Praxair Technology, Inc. Central carbon dioxide purifier
US7291271B2 (en) * 2003-12-09 2007-11-06 Separation Design Group, Llc Meso-frequency traveling wave electro-kinetic continuous adsorption system
RU2440179C2 (en) * 2005-03-17 2012-01-20 НОКС II ИНТЕНЭШНЛ, эЛТиДи. Method of reducing content of sulphur and/or mercury in flue gases (versions), sorbent composition, method of burning coal with reduced emission of harmful elements into environment (versions), coal ash obtained using said methods, and cement, pozzolan, concrete mixture and mortar thereof, concrete structure, method of producing cementing mixture, obtained based on or through said ash
ES2604080T3 (en) * 2007-01-17 2017-03-02 Union Engineering A/S High purity carbon dioxide recovery procedure
US20080271466A1 (en) * 2007-05-01 2008-11-06 Giacobbe Frederick W Method and System for Purifying Liquified Gases
US8980211B2 (en) * 2008-03-01 2015-03-17 Bryan Christopher Timmins Method for the capture and disposal of carbon dioxide in an energy conversion process

Patent Citations (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2039330A (en) * 1930-07-08 1936-05-05 Ralph H Mckee Purification of carbon dioxide
US3074245A (en) * 1957-07-18 1963-01-22 Linde Eismasch Ag Process for the selective removal of carbon dioxide and hydrogen sulfide from gaseous mixtures containing the same
US3001373A (en) * 1958-04-11 1961-09-26 Texaco Inc Separation of carbon dioxide from gaseous mixtures
US3421984A (en) * 1967-05-02 1969-01-14 Susquehanna Corp Purification of fluids by selective adsorption of an impure side stream from a distillation with adsorber regeneration
US4052176A (en) * 1975-09-29 1977-10-04 Texaco Inc. Production of purified synthesis gas H2 -rich gas, and by-product CO2 -rich gas
US4270937A (en) * 1976-12-01 1981-06-02 Cng Research Company Gas separation process
US4144038A (en) * 1976-12-20 1979-03-13 Boc Limited Gas separation
US4759848A (en) * 1985-01-23 1988-07-26 Mg Industries Sterilization of cryogenic liquids by ultrafiltration
US4784672A (en) * 1987-10-08 1988-11-15 Air Products And Chemicals, Inc. Regeneration of adsorbents
US5100635A (en) * 1990-07-31 1992-03-31 The Boc Group, Inc. Carbon dioxide production from combustion exhaust gases with nitrogen and argon by-product recovery
US5837032A (en) * 1991-01-30 1998-11-17 The Cynara Company Gas separations utilizing glassy polymer membranes at sub-ambient temperatures
US5271760A (en) * 1993-03-01 1993-12-21 Uop Recovery of liquid mercury from process streams
US5450728A (en) * 1993-11-30 1995-09-19 Air Products And Chemicals, Inc. Recovery of volatile organic compounds from gas streams
US5925326A (en) * 1995-08-23 1999-07-20 The Boc Group, Inc. Process for the production of high purity carbon dioxide
US6119480A (en) * 1998-01-23 2000-09-19 L'air Liquide, Societe Anonyme Pour L'etude Et L'exploitation Des Procedes Georges Claude Plant and method for liquid-phase filtration of a cryogenic fluid
US6511528B1 (en) * 1999-03-26 2003-01-28 Uop Llc Purification of carbon dioxide
US20090101007A1 (en) * 2004-10-08 2009-04-23 Rasmus Find Method for recovery of carbon dioxide from a gas
US7556671B2 (en) * 2005-08-08 2009-07-07 The Boc Group, Inc. System and method for purifying a gas
US20080173585A1 (en) * 2007-01-23 2008-07-24 Vincent White Purification of carbon dioxide
US20090013868A1 (en) * 2007-07-11 2009-01-15 Arthur Darde Process and apparatus for the separation of a gaseous mixture
US20090013871A1 (en) * 2007-07-11 2009-01-15 Arthur Darde Process and apparatus for the separation of a gaseous mixture
WO2009010690A2 (en) * 2007-07-13 2009-01-22 L'air Liquide Societe Anonyme Pour L'etude Et L'exploitation Des Procedes Georges Claude Method for the purification of a gas containing co2
US8465570B2 (en) * 2007-07-13 2013-06-18 L'air Liquide Societe Anonyme Pour L'etude Et L'exploitation Des Procedes Georges Claude Method for the purification of a gas containing CO2

Cited By (3)

* Cited by examiner, † Cited by third party
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

Similar Documents

Publication Publication Date Title
US10960343B2 (en) Methods and systems for performing chemical separations
US11186529B2 (en) Advanced oxidative coupling of methane
CN105749699B (en) Full-temperature-range pressure swing adsorption gas separation, purification and purification method
Ebner et al. State-of-the-art adsorption and membrane separation processes for carbon dioxide production from carbon dioxide emitting industries
AU2010298708B2 (en) Maintaining low carbon monoxide levels in product carbon dioxide
CA2925555C (en) Carbon dioxide recovery
WO2017006724A1 (en) Source gas purification apparatus and purification method
AU2011226389A1 (en) Method for the absorptive drying of purified biogas and for regenerating laden adsorbents
WO2007007571A1 (en) Method for removal of sulfur-containing compound from natural gas
JP2009504875A (en) Method and apparatus for purification of a methane-rich gas stream
WO2019005716A1 (en) Process for gas separation by solvent or absorbent
CN102626580A (en) Two-step pressure swing adsorption separation method of multicomponent gas containing hydrogen and hydrogen sulfide
CA2769495C (en) Process for removing harmful substances from carbon dioxide and apparatus for the performance thereof
AU2010328581B2 (en) Maintaining lowered CO in a CO2 product stream in a process for treating synthesis gas
EP3808431A1 (en) Process and plant for deacidifying a fluid stream comprising sulfur compounds, including organic sulfur compounds
WO2020174858A1 (en) Carbon dioxide production method, and device for producing carbon dioxide
JP2010209296A (en) Method for removing organic sulfur compound in raw material gas, and catalyst used in the method
EA014385B1 (en) Process for producing a gas stream depleted of mercaptans
Sahota et al. Bioresource Technology Reports
Pirngruber et al. Opportunities for MOFs in CO2 capture from flue gases, natural gas, and syngas by adsorption
Ghoshal et al. Capturing CO2 by Physical and Chemical Means
JP2010174191A (en) Method for reducing oxygen consumption in natural gas treatment
JP2010209297A (en) Two-step method for treating organic sulfur compound contained in natural gas

Legal Events

Date Code Title Description
AS Assignment

Owner name: SIEMENS AKTIENGESELLSCHAFT, GERMANY

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:BALDAUF, MANFRED;GRAEBER, CARSTEN;HANEBUTH, MARC;AND OTHERS;SIGNING DATES FROM 20111202 TO 20111207;REEL/FRAME:027548/0852

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION