US20180023888A1 - Method for recovering helium - Google Patents
Method for recovering helium Download PDFInfo
- Publication number
- US20180023888A1 US20180023888A1 US15/549,854 US201615549854A US2018023888A1 US 20180023888 A1 US20180023888 A1 US 20180023888A1 US 201615549854 A US201615549854 A US 201615549854A US 2018023888 A1 US2018023888 A1 US 2018023888A1
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- United States
- Prior art keywords
- nitrogen
- fraction
- helium
- enriched fraction
- enriched
- 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
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- 239000001307 helium Substances 0.000 title claims abstract description 48
- 229910052734 helium Inorganic materials 0.000 title claims abstract description 48
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 title claims abstract description 47
- 238000000034 method Methods 0.000 title claims abstract description 35
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract description 132
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 66
- 238000000926 separation method Methods 0.000 claims abstract description 29
- UDWPONKAYSRBTJ-UHFFFAOYSA-N [He].[N] Chemical compound [He].[N] UDWPONKAYSRBTJ-UHFFFAOYSA-N 0.000 claims abstract description 17
- 239000007789 gas Substances 0.000 claims abstract description 16
- 230000000274 adsorptive effect Effects 0.000 claims abstract description 9
- 238000004140 cleaning Methods 0.000 claims description 6
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 14
- 239000007788 liquid Substances 0.000 description 9
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 230000003647 oxidation Effects 0.000 description 4
- 238000007254 oxidation reaction Methods 0.000 description 4
- 230000003197 catalytic effect Effects 0.000 description 3
- 238000005202 decontamination Methods 0.000 description 3
- 230000003588 decontaminative effect Effects 0.000 description 3
- 230000008929 regeneration Effects 0.000 description 3
- 238000011069 regeneration method Methods 0.000 description 3
- 229910052786 argon Inorganic materials 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 239000007792 gaseous phase Substances 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- 239000003345 natural gas Substances 0.000 description 2
- 229910052756 noble gas Inorganic materials 0.000 description 2
- 150000002835 noble gases Chemical class 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 150000002371 helium Chemical class 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000013526 supercooled liquid Substances 0.000 description 1
- 230000000153 supplemental effect Effects 0.000 description 1
- 230000007306 turnover Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
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- F25J3/0228—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by rectification, i.e. by continuous interchange of heat and material between a vapour stream and a liquid stream characterised by the separated product stream
- F25J3/028—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by rectification, i.e. by continuous interchange of heat and material between a vapour stream and a liquid stream characterised by the separated product stream separation of noble gases
- F25J3/029—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by rectification, i.e. by continuous interchange of heat and material between a vapour stream and a liquid stream characterised by the separated product stream separation of noble gases of helium
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- F25J3/0257—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by rectification, i.e. by continuous interchange of heat and material between a vapour stream and a liquid stream characterised by the separated product stream separation of nitrogen
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Definitions
- the invention relates to a method for recovering a helium product fraction from a nitrogen- and helium-containing feed fraction, wherein
- helium product fraction be comprised of highly purified helium, the concentration and contamination of which do not exceed a value of 100 vppm, preferably of 10 vppm.
- nitrogen- and helium-containing feed fraction be understood as a fraction, which contains 1 to 20 mol-% helium and 80 to 99 mol-% nitrogen. Further, this feed fraction can contain 0.1 to 2 mol-% methane and traces of hydrogen, argon and/or other noble gases.
- helium is obtained almost exclusively from a mixture of volatile natural gas components, which typically contains methane and nitrogen as well as traces of hydrogen, argon and other noble gases besides helium.
- concentration of this decontamination in helium cannot exceed a value of 100 vppm, preferably of 10 vppm.
- the helium purification prior to the actual helium liquefaction generally consists of a combination of cryogenic—based on partial condensation—and adsorptive methods with regeneration through pressure and/or temperature changes. Based on the comparatively high product value, a helium yield as high as possible, preferably >99%, is desirable. In consequence, the helium-enriched fraction is often transferred from the liquid into the gaseous phase by pressure release and/or stripping from the liquid to the gaseous phase during the cryogenic step to remain available for further processing.
- a nitrogen- and helium-containing feed fraction which originates, for example, from a separation process of natural gas, is first supplied to catalytic methane oxidation A and subsequently via line 2 to a drying unit B.
- the water separated in the drying unit B is removed via line 30 .
- the feed fraction conventionally pretreated in such way which typically has a pressure of between 10 and 40 bar, preferably between 15 and 25 bar, is supplied to the heat exchanger E 1 via line 3 and partially condensed therein against method flows yet to be explained.
- the partially condensed feed fraction is supplied to a separator D 1 and separated therein into a first helium-enriched fraction 5 as well as a first nitrogen-enriched fraction 8 .
- the helium-enriched fraction 5 is supplied to an adsorptive cleaning process D after preheating in the heat exchanger E 1 .
- Such process is designed as (V)PSA and/or TSA process.
- the helium-enriched fraction recovered therein and removed via line 6 represents the helium product fraction, the concentration of decontamination of which does not exceed a value of 100 vppm, preferably of 100 vppm.
- this helium product fraction is supplied to a liquefaction process not illustrated in FIG. 1 .
- the helium-containing residue gas removed from the adsorptive cleaning process D is supplied to a return compressor C via line 7 , is compressed therein to the pressure of the feed fraction 1 to be supplied to the catalytic methane oxidation A and admixed thereto via line 32 .
- the above mentioned first nitrogen-enriched fraction 8 is expanded in valve a and supplied to the separation column T in its upper section as return flow.
- the separation column T is preferably operated at a pressure between 7 and 20 bar, in particular between 10 and 15 bar.
- a separation into a second helium-enriched gas fraction 9 and a second nitrogen-enriched liquid fraction 11 is implemented therein.
- the second helium-enriched fraction 9 is preheated in heat exchanger E 1 against the feed fraction 3 to be partially condensed, and supplied to the mentioned return compressor C via control valve b, as well. Additional air is supplied thereto via line 31 .
- the oxygen contained in the air serves as oxidation means for the catalytic methane oxidation A.
- a sub-flow of the second nitrogen-enriched liquid fraction 11 is evaporated in heat exchanger E 1 and supplied to the separation column T as stripping gas 12 .
- Such stripping gas supply causes the separation process taking place in separation column T and determines the helium content of the second helium-enriched fraction 9 .
- At least a sub-flow of the second nitrogen-enriched fraction 11 is evaporated in heat exchanger E 1 against the feed fraction to be partially condensed 3 under a pressure of less than 5 bar, preferably of less than 3 bar.
- This method serves to set a temperature as low as possible in separator D 1 .
- a sub-flow of the second nitrogen-enriched fraction 11 is supplied to a circulation container D 2 via control valve c.
- the liquid fraction removed therefrom via line 14 is supplied to heat exchanger E 1 under the above mentioned low pressure, at least partially evaporated therein, and resupplied to the circulation container D 2 .
- a nitrogen-enriched gas fraction 15 is removed from the top of circulation container D 2 , preheated in heat exchanger E 1 against the feed fraction to be partially condensed 3 , and subsequently resupplied as regeneration gas to the above mentioned drying unit B, which is an adsorptive drying process, as a rule.
- This loaded regeneration gas is removed from the process via line 16 .
- the sub-flow 13 of the second nitrogen-enriched fraction 11 which is not supplied to the circulation container D 2 , can be supercooled in heat exchanger E 1 and can be generated as supercooled liquid via control valve d and line 17 .
- an otherwise required generation or provision of liquefied nitrogen (LIN), as the case may be, can be refrained from.
- a sub-flow of liquid fraction 14 removed from the circulation container D 2 can be removed in the above described manner via control valve d and line 17 .
- the coldness required for the partial condensation of the feed fraction 3 can principally be provided by preheating cold, gaseous decomposition products as well as the above described evaporation of liquid fraction 14 , which was removed from the circulation container D 2 .
- the larger the stripping gas quantity 12 evaporated in heat exchanger E 1 the lower can be the quantity of liquid fraction 14 removed from the circulation container D 2 . It must, however, be ensured that heat exchange and temperature of flow 12 are suitable for cooling and partially condensing feed fraction 3 . If the content of flow 12 in the heat turnover in heat exchanger E 1 becomes too large, the temperature in separator D 1 increases undesirably.
- the quantity of the stripping gas 12 supplied to separation column T is selected according to the invention to such amount that a third nitrogen-enriched fraction 20 can be removed from separation column T in the section of its bottom, wherein such fraction contains at least 30%, preferably at least 50% of the nitrogen contained in the first nitrogen-enriched fraction 8 .
- These nitrogen contents are achieved in that a larger stripping gas quantity 12 is boiled up in the bottom of separation column T than would be required for the actual stripping process in separation column T.
- a further nitrogen-enriched fraction can be recovered in separation column T under increased pressure.
- This further or third nitrogen-enriched fraction can be condensed to a pressure after preheating in heat exchanger E 1 , which is above the pressure of column T by 4 to 20 bar, preferably by 5 to 15 bar.
- the nitrogen-enriched fraction 21 is cooled in heat exchanger E 1 and subsequently work-performing expanded in expansion device X.
- the expanded nitrogen-enriched fraction 22 is subsequently preheated against the feed fraction to be partially condensed 3 in heat exchanger E 1 and admixed to the above described nitrogen-enriched fraction 15 .
- Such work-performing expansion X which increases thermo-dynamic efficiency of the process, is optional, facilitates or increases the quantity of the cooled liquid (LIN) removed via line 17 , however.
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- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Mechanical Engineering (AREA)
- Thermal Sciences (AREA)
- General Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Separation By Low-Temperature Treatments (AREA)
- Separation Of Gases By Adsorption (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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DE102015001664.4A DE102015001664A1 (de) | 2015-02-10 | 2015-02-10 | Verfahren zur Heliumgewinnung |
DE102015001664.4 | 2015-02-10 | ||
PCT/EP2016/000131 WO2016128111A1 (de) | 2015-02-10 | 2016-01-26 | Verfahren zur heliumgewinnung |
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US (1) | US20180023888A1 (ru) |
AU (1) | AU2016218602B2 (ru) |
CA (1) | CA2976341C (ru) |
DE (1) | DE102015001664A1 (ru) |
RU (1) | RU2689252C2 (ru) |
WO (1) | WO2016128111A1 (ru) |
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FR3096900B1 (fr) * | 2019-06-06 | 2021-10-01 | Air Liquide | Procédé et unité de purification d’hélium |
Citations (4)
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US5351491A (en) * | 1992-03-31 | 1994-10-04 | Linde Aktiengesellschaft | Process for obtaining high-purity hydrogen and high-purity carbon monoxide |
US5771714A (en) * | 1997-08-01 | 1998-06-30 | Praxair Technology, Inc. | Cryogenic rectification system for producing higher purity helium |
DE10007440A1 (de) * | 2000-02-18 | 2001-08-23 | Linde Ag | Verfahren zum Abtrennen einer Helium-reichen Fraktion aus einem wenigstens Methan, Stickstoff und Helium enthaltenden Strom |
US20080272340A1 (en) * | 2005-02-01 | 2008-11-06 | Daphne Koh | Method for Producing Syngas with Low Carbon Dioxide Emission |
Family Cites Families (11)
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US3205669A (en) * | 1960-08-15 | 1965-09-14 | Phillips Petroleum Co | Recovery of natural gas liquids, helium concentrate, and pure nitrogen |
SU1645796A1 (ru) * | 1989-01-26 | 1991-04-30 | Всесоюзный научно-исследовательский институт природных газов | Способ одновременного получени гели , этана и более т желых углеводородов |
US5167125A (en) | 1991-04-08 | 1992-12-01 | Air Products And Chemicals, Inc. | Recovery of dissolved light gases from a liquid stream |
US5257505A (en) * | 1991-04-09 | 1993-11-02 | Butts Rayburn C | High efficiency nitrogen rejection unit |
DE10106484A1 (de) * | 2001-02-13 | 2002-08-14 | Linde Ag | Verfahren zum gleichzeitigen Gewinnen einer Helium- und einer Stickstoff-Reinfraktion |
DE102005010054A1 (de) * | 2005-03-04 | 2006-09-07 | Linde Ag | Verfahren zum gleichzeitigen Gewinnen einer Helium- und einer Stickstoff-Reinfraktion |
DE102008007925A1 (de) * | 2008-02-07 | 2009-08-13 | Linde Aktiengesellschaft | Verfahren zur Helium-Gewinnung |
DE102011010634A1 (de) * | 2011-02-08 | 2012-08-09 | Linde Aktiengesellschaft | Verfahren zum Abtrennen von Spurenkomponenten aus einer wenigstens Stickstoff und Helium enthaltenden Fraktion |
DE102012008446A1 (de) * | 2012-04-26 | 2013-10-31 | Linde Aktiengesellschaft | Abtrennen von Helium aus einer Methan-reichen Fraktion |
DE102013007208A1 (de) * | 2013-04-25 | 2014-10-30 | Linde Aktiengesellschaft | Verfahren zum Gewinnen einer Methan-reichen Flüssigfraktion |
DE102013012656A1 (de) * | 2013-07-30 | 2015-02-05 | Linde Aktiengesellschaft | Verfahren zum Abtrennen unerwünschter Komponenten aus einem Helium-Strom |
-
2015
- 2015-02-10 DE DE102015001664.4A patent/DE102015001664A1/de not_active Withdrawn
- 2015-06-22 RU RU2015124169A patent/RU2689252C2/ru active
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2016
- 2016-01-26 AU AU2016218602A patent/AU2016218602B2/en active Active
- 2016-01-26 US US15/549,854 patent/US20180023888A1/en not_active Abandoned
- 2016-01-26 CA CA2976341A patent/CA2976341C/en active Active
- 2016-01-26 WO PCT/EP2016/000131 patent/WO2016128111A1/de active Application Filing
Patent Citations (4)
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US5351491A (en) * | 1992-03-31 | 1994-10-04 | Linde Aktiengesellschaft | Process for obtaining high-purity hydrogen and high-purity carbon monoxide |
US5771714A (en) * | 1997-08-01 | 1998-06-30 | Praxair Technology, Inc. | Cryogenic rectification system for producing higher purity helium |
DE10007440A1 (de) * | 2000-02-18 | 2001-08-23 | Linde Ag | Verfahren zum Abtrennen einer Helium-reichen Fraktion aus einem wenigstens Methan, Stickstoff und Helium enthaltenden Strom |
US20080272340A1 (en) * | 2005-02-01 | 2008-11-06 | Daphne Koh | Method for Producing Syngas with Low Carbon Dioxide Emission |
Also Published As
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RU2015124169A3 (ru) | 2018-10-29 |
RU2015124169A (ru) | 2017-01-10 |
DE102015001664A1 (de) | 2016-08-11 |
WO2016128111A1 (de) | 2016-08-18 |
AU2016218602A1 (en) | 2017-08-31 |
AU2016218602B2 (en) | 2021-04-08 |
RU2689252C2 (ru) | 2019-05-24 |
CA2976341C (en) | 2023-07-11 |
CA2976341A1 (en) | 2016-08-18 |
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