WO2012000727A1 - Verfahren zur trennung von gasen - Google Patents
Verfahren zur trennung von gasen Download PDFInfo
- Publication number
- WO2012000727A1 WO2012000727A1 PCT/EP2011/058636 EP2011058636W WO2012000727A1 WO 2012000727 A1 WO2012000727 A1 WO 2012000727A1 EP 2011058636 W EP2011058636 W EP 2011058636W WO 2012000727 A1 WO2012000727 A1 WO 2012000727A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- stream
- permeate
- retentate
- gas
- separation
- Prior art date
Links
- 238000000926 separation method Methods 0.000 title claims abstract description 189
- 239000007789 gas Substances 0.000 title claims description 164
- 238000000034 method Methods 0.000 title claims description 52
- 239000012528 membrane Substances 0.000 claims abstract description 114
- 239000000203 mixture Substances 0.000 claims abstract description 55
- 239000012465 retentate Substances 0.000 claims description 170
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 165
- 239000012466 permeate Substances 0.000 claims description 165
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 90
- 229910002092 carbon dioxide Inorganic materials 0.000 claims description 47
- 239000001569 carbon dioxide Substances 0.000 claims description 45
- 239000004642 Polyimide Substances 0.000 claims description 19
- 229920001721 polyimide Polymers 0.000 claims description 19
- 230000006835 compression Effects 0.000 claims description 16
- 238000007906 compression Methods 0.000 claims description 16
- 239000012510 hollow fiber Substances 0.000 claims description 15
- 239000000047 product Substances 0.000 claims description 10
- 239000000463 material Substances 0.000 claims description 6
- 239000001257 hydrogen Substances 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 4
- 229920006380 polyphenylene oxide Polymers 0.000 claims description 4
- 229910002091 carbon monoxide Inorganic materials 0.000 claims description 3
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 2
- 239000004952 Polyamide Substances 0.000 claims description 2
- -1 Polysiloxanes Polymers 0.000 claims description 2
- 229920002301 cellulose acetate Polymers 0.000 claims description 2
- 239000004941 mixed matrix membrane Substances 0.000 claims description 2
- 229920002492 poly(sulfone) Polymers 0.000 claims description 2
- 229920002647 polyamide Polymers 0.000 claims description 2
- 229920000642 polymer Polymers 0.000 claims description 2
- 229920001451 polypropylene glycol Polymers 0.000 claims description 2
- 229920001296 polysiloxane Polymers 0.000 claims description 2
- 238000010926 purge Methods 0.000 claims description 2
- 229920001887 crystalline plastic Polymers 0.000 claims 1
- 238000012958 reprocessing Methods 0.000 claims 1
- 238000002156 mixing Methods 0.000 description 19
- 239000003345 natural gas Substances 0.000 description 11
- 238000004064 recycling Methods 0.000 description 7
- 238000000746 purification Methods 0.000 description 6
- 230000008901 benefit Effects 0.000 description 5
- 239000004033 plastic Substances 0.000 description 4
- 229920003023 plastic Polymers 0.000 description 4
- 238000001556 precipitation Methods 0.000 description 4
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 238000004140 cleaning Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 230000000717 retained effect Effects 0.000 description 3
- 238000001179 sorption measurement Methods 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 229920001108 Polyimide P84 Polymers 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000011144 upstream manufacturing Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 229910001868 water Inorganic materials 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 241000532841 Platanus orientalis Species 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000012444 downstream purification process Methods 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000005431 greenhouse gas Substances 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000005201 scrubbing Methods 0.000 description 1
- 239000000565 sealant Substances 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
- B01D53/22—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 diffusion
- B01D53/225—Multiple stage diffusion
-
- 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
- B01D53/22—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 diffusion
- B01D53/225—Multiple stage diffusion
- B01D53/226—Multiple stage diffusion in serial connexion
-
- 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
- B01D53/22—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 diffusion
- B01D53/225—Multiple stage diffusion
- B01D53/227—Multiple stage diffusion in parallel connexion
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D61/00—Processes of separation using semi-permeable membranes, e.g. dialysis, osmosis or ultrafiltration; Apparatus, accessories or auxiliary operations specially adapted therefor
- B01D61/58—Multistep processes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D63/00—Apparatus in general for separation processes using semi-permeable membranes
- B01D63/02—Hollow fibre modules
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D63/00—Apparatus in general for separation processes using semi-permeable membranes
- B01D63/08—Flat membrane modules
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D71/00—Semi-permeable membranes for separation processes or apparatus characterised by the material; Manufacturing processes specially adapted therefor
- B01D71/06—Organic material
- B01D71/58—Other polymers having nitrogen in the main chain, with or without oxygen or carbon only
- B01D71/62—Polycondensates having nitrogen-containing heterocyclic rings in the main chain
- B01D71/64—Polyimides; Polyamide-imides; Polyester-imides; Polyamide acids or similar polyimide precursors
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L3/00—Gaseous fuels; Natural gas; Synthetic natural gas obtained by processes not covered by subclass C10G, C10K; Liquefied petroleum gas
- C10L3/06—Natural gas; Synthetic natural gas obtained by processes not covered by C10G, C10K3/02 or C10K3/04
- C10L3/10—Working-up natural gas or synthetic natural gas
- C10L3/101—Removal of contaminants
- C10L3/102—Removal of contaminants of acid contaminants
- C10L3/104—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
- B01D2256/24—Hydrocarbons
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2257/00—Components to be removed
- B01D2257/50—Carbon oxides
- B01D2257/504—Carbon dioxide
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02C—CAPTURE, STORAGE, SEQUESTRATION OR DISPOSAL OF GREENHOUSE GASES [GHG]
- Y02C20/00—Capture or disposal of greenhouse gases
- Y02C20/40—Capture or disposal of greenhouse gases of CO2
Definitions
- the invention relates to a special device
- Plastics generally become hollow fibers or
- the separation result achievable with a membrane in a simple passage depends not only on the selectivity of the membrane but also on the pressure ratio between the high-pressure side and the low-pressure side of the membrane. The larger the pressure ratio, the better the maximum achievable separation result.
- the amount of slippage or loss of methane is correspondingly high.
- Methane yield can be improved.
- Target product stream the natural gas depleted of acid gases.
- the permeate side, acid gas enriched stream is
- EP0 799 634 discloses an interconnection according to Fig. 8.
- a disadvantage is an additional potential entry of oil or water as a sealant and lubricant, additional high investment costs, increased energy consumption due to additional compression and increased
- Fig. 9 shows a technology that is frequently proposed and implemented, in particular for the treatment of biogas (Air Liquide and Harasek). One is revealed
- EP 0 603 798 discloses a multi-stage interconnection for the production of nitrogen.
- the disadvantage of this method is the insufficient purity of the permeating component as well as the use of at least two
- EP0695574 discloses an interconnection with partial use of a permeate stream as sweep stream for the production of a purest possible retentate.
- a disadvantage of this method is the inadequate quality of Bacpermeats.
- EP1634946 discloses a process for the treatment of biogas. This describes a thermal utilization of methane from the methane-depleted stream. Disadvantages are the high costs and the loss of the gas.
- EP0596268 discloses various interconnections for producing three different gas compositions
- Permeate gas or a high purity of the retentate gas can be achieved.
- Recompression unit or without further purification of the permeate or retentate stream (e.g., thermal
- the object of the present invention was to devices and
- an as universally applicable / -able method / device for any gas mixtures should be provided.
- a further specific object of the present invention was to provide a method or apparatus which makes it possible to purify methane-containing crude gas streams, with a reduced methane emission compared with the prior art methods, with the same throughput, and thus a reduced environmental impact through this strong greenhouse gas.
- the device according to claim 1 or one of the dependent claims can provide pure streams of permeate and retentate, without more than one compressor is required or the permeate or retentate must be further purified by other methods.
- the device according to the invention thus makes it possible to simultaneously achieve permeate and retentate streams in high purity.
- the investment costs for the system are low, it does not require any additional downstream purification process. It was thus possible to solve the tasks with a pure membrane separation process.
- permeate gas is / are enriched respectively on the membrane, on the membrane module, or in the membrane separation step in the permeate stream relative to the respective inlet stream
- Membrane membrane modules or membrane separation step resulting stream called that does not pass through the membrane.
- Retentatgas is / are in each case at the membrane, at the membrane module, or in the membrane separation step in
- Raw gas or crude gas mixture or crude gas stream (17) denotes a gas mixture of at least two gases or a stream of this gas mixture, the / by means of the invention
- Feed stream (5) denotes a gas stream which is the
- Feed current separation stage (1) is supplied.
- This stream can be too the implementation of the method correspond to the crude gas stream (17) or compressed by a compressor crude gas stream.
- the feed stream (5) is composed of the gases of the crude gas stream (17), the second permeate stream (9) and the third retentate stream (10).
- the feed stream (5) can be generated in which the streams (9) and (10) are mixed either with the uncompressed crude gas stream (17) or both with the compressed raw gas stream or one with the uncompressed and one with the compressed crude gas stream the streams (9) and / or (10) are mixed in the compressor with the raw gas stream (17).
- Feedstromtrennstu e (1) denotes a membrane separation stage for separating the feed stream (5) into a first permeate and a first retentate stream (6) or (7).
- Retentattrennstu e (2) denotes a membrane separation stage which may be the same or different to the feed current separation stage (1), for the separation of the first
- Permeattrennstu e (3) denotes a membrane separation stage which may be the same or different to the feed stream separation stage (1) or retentate separation stage (2), for separating the first permeate stream (6) into a third permeate and a third retentate stream (11) and ( 10).
- FIG. 11 to 13 includes a concatenation of three membrane separation stages.
- Each stage consists of one or more physical gas separation modules connected in parallel and / or in series within one stage.
- As a driving force for the gas separation in the modules a partial pressure difference between the retentate and the
- the partial pressure difference can either by means of a
- Feed stream separation stage (1) is arranged and / or by means of at least one, preferably one or two vacuum pump (s) (not shown in Figs. 11 to 13) preferably on the
- Permeattrenncut (3) in the third permeate stream (11) are generated. Possibly. For example, it may be advantageous to generate or enhance the partial pressure difference in one or more of the membrane separation stages by means of a permeate-side purge gas stream.
- a compressor (4) brings the crude gas mixture or the gas mixture from the raw gas stream (17) and the second permeate stream (9) and / or the third retentate stream (10) to the desired pressure in the region of 5 to 100 bar, but preferably to a pressure of 9 to 75 bar.
- the resulting feed stream (5) is introduced into the feed stream separation stage (1).
- the feed current separation stage (1) is a
- retentate gas permeating components
- the inventive method and the device according to the invention is characterized in that it / is designed such that the concentration of at least one permeate gas of the feed stream separation stage (1), after recycling the second permeate stream (9) and the third retentate stream (10) Feed stream (5) is increased, preferably by at least 2%, more preferably by at least 3% and most preferably by 3 to 40%, each in comparison to
- the increase may depend on the composition of the crude gas stream (17) and is particularly pronounced at low concentrations of a permeate gas (10 to 20%). Usually this is the
- Feed stream separation stage (1) when the concentration of at least one in the feed stream separation stage (1) more easily permeating component A or a permeate A in the feed stream (5) is increased. Similarly, a reduction was noted when the concentration of component A or a
- Permeate gas A in the feed stream (5) to be purified between 10 and 60%, preferably between 15 and 55% and particularly preferably between 20 and 50%.
- Permeate gas A in the feed stream (5) to be purified between 10 and 60%, preferably between 15 and 55% and particularly preferably between 20 and 50%.
- the inventive method and the device according to the invention therefore designed such that the content of permeate gas (s) of the feed stream separation stage (1) in the feed stream (5) at greater than or equal to 40 vol.%, Preferably more than 50 Vol.% And especially at more than 55 vol.% Based on the volume of the feed stream (5), after recycling the second
- Feed stream (5) increases the efficiency of the feed stream separation stage (1), which in turn results in less retentate gas B entering the first permeate stream (6). This in turn increases the efficiency of the
- Permeattrenncut (3) ensures that less unwanted retentate passes into the third permeate stream (10) here.
- this leads to the advantage that the undesirable emissions of climate-damaging methane could be significantly reduced.
- it can be said that in the feed stream separation stage (1), preferably 20 to 100%, more preferably 40 to 70% of component A or a permeate gas A is transferred from the feed stream (5) into the permeate.
- the retentate of the feedstream separation stage (1) is optionally depressurized by an optional existing one
- Retentate side of the retentate separation step (2), i. in the second retentate stream (8), is preferably a
- the content of the heavier permeating components or of a retentate gas B is further increased in the retentate separation stage (2) so that the content of component B or of a retentate gas B in the second retentate stream (8) is more than 90%, preferably more than 95% and particularly preferably more than 97%.
- the invention is characterized
- Feed stream separation stage (1) via the second retentate stream (8) are discharged.
- the step separation section of the retentate separation step (2) is at a concentration of component A or one Permeate gas A of 50% in the first retentate stream (7) between 10 and 60%, preferably between 20 and 50%.
- the permeate of the retentate separation stage (2) is recycled by means of the second permeate stream (9), fed to the feed stream (5) and recycled.
- This can - as previously in the definition of the term "feed stream” already explained - depending on whether a compressor (4) or even a multi-stage compressor (4) is used in different ways second permeate stream (9) preferably the suction side of
- Compressor (4) (see Fig. 11) supplied. Becomes a
- the second permeate stream (9) is introduced between two compression stages in the compressor (see Fig. 12 and 13).
- the highly enriched with the component A or a permeate A permeate Feedstromtrenncut (1) is supplied by means of the first permeate stream (6) of the permeate separation stage (3). If necessary, by means of a
- Permeate separation stage (3) i. the third retentate stream (10), prevent the pressure of the permeate the
- Feed stream separation stage (1) drops to ambient pressure (see Fig. 11). In this way, the driving force for the
- Permeate separation stage (3) are retained.
- the permeate separation stage (3) produces a permeate with a content of component B or a retentate gas B greater than 95%, preferably greater than 97% and particularly preferably greater than 99%, which via the third permeate stream (11) from the Device is discharged.
- the inventive form is
- Feed stream separation stage (1) via the third permeate stream (11) are discharged.
- the step separation cut of the permeate separation stage (3) is between 50 and 95%, preferably between 70 and 93%.
- the third retentate stream (10) is recycled, the
- Feed stream (5) supplied and reprocessed This can, as already explained above, take place in different ways and z. B. depending on whether a compressor (4) or even a multi-stage compressor (4) is used.
- the third retentate stream (10) is preferably fed to the suction side of the compressor (4) (see Fig. 11). If a multi-stage compressor is used, it is preferred that the third retentate stream (10) be introduced into the compressor between two stages of compression (see Figures 12 and 13).
- the Device is characterized in particular by the fact that it / is designed such that in the second permeate stream (9) and in the third retentate stream (10) recycled gas volume in total less than 60 vol.%, Preferably 10 to 50 vol.%, Whole more preferably 20 to 40% by volume of the volume of the Crude gas flow (17) is.
- the control of the amount of Retentatgasströme to be recycled may, for. B. by selecting the respective membrane modules in the membrane separation stages (1) to (3) or controlled by the pressures in the system or by the rivers.
- the method according to the invention or the device is characterized in that, despite very low reflux currents, the above-explained increase in the concentration of the permeate component in the feed stream (5)
- the first permeate stream (6) is preferably conducted so that the feed pressure of the permeate separation stage (3), preferably by means of a pressure reducing valve (14) on the retentate side of
- Permeattrenncut (3) between 1 and 30 bar, preferably between 2 and 20 bar and particularly preferably 3 and 10 bar betiller.
- the retentate separation stage (2) would normally be operated in the range of selectivity limited to relaxation at feed pressure, it may be expedient to use the second permeate stream (9) only to a higher pressure level of a multistage Pressure booster unit, ie a multi-stage compressor (4) to relax because thus the operating costs of
- a multi-stage compressor (4) is used and the gas streams (9) and (10) are used in each case between two compressors
- the device according to the invention can have one or more pressure-reducing valves (12), (13) or (14).
- Feed stream separation stage (1), to 1 and 30 bar, preferably between 2 and 20 bar and more preferably between 3 and 10 bar is limited. At the same time or alternatively, it is ensured, preferably by means of a pressure reducing valve (13), that the pressure drop across the
- Feed stream separation stage (1) and the retentate separation stage (2), to 1 and 100 bar, preferably between 5 and 80 bar and particularly preferably between 10 and 70 bar is limited.
- the inventive device or the inventive method can be realized in principle with all membranes that are capable of binary gas mixtures or
- membrane materials are preferably but not exclusively plastics used.
- plastics in the separating active layer are particularly preferably polyimides, polyamides, polysulfones, cellulose acetates and derivatives, polyphenylene oxides, polysiloxanes, polymers with intrinsic microporosity, mixed matrix membranes,
- Polypropylene oxides, carbon membranes or zeolites or mixtures thereof in question are polypropylene oxides, carbon membranes or zeolites or mixtures thereof in question.
- Particularly preferred membranes have as materials for the separation-active layer or as a material for the complete
- R is selected from the group consisting of
- x, y molar fraction with 0 ⁇ x ⁇ 0.5 and 1>y> 0.5.
- Such membranes are available from Evonik Fibers GmbH under the name polyimide P84 and polyimide P84 HT. A process for the preparation of these preferred membranes is disclosed in WO 2011/009919 Al. All disclosed in this disclosure membranes can in methods according to the invention are preferably used. To avoid pure repetition, the content of this patent application is hereby fully incorporated by reference. It has been found that with these membranes the best
- the membranes are preferably used in the form of hollow fiber membranes and / or flat membranes.
- the membranes are installed in modules, which are then used in the separation task.
- modules all known in the art
- Gas separation modules such as but not
- Spiral cradle gas separation modules cushion gas separation modules or tube bundle gas separation modules are used.
- Membrane of at least 30, preferably at least 35,
- Permeate separation stage (3) must be returned. Thus, especially when using a single-stage compressor (4) less gas must be compressed twice, which brings economic benefits in the operation of the system with it. For very selective membrane modules with a selectivity of 45, only about 35% of the crude gas needs to be in the feedstream separation stage (1) injected gas can be compressed twice, with a membrane module with a selectivity of only 10, it may be that the double compression is up to 300%.
- the figures 35% and 300% relate to experiments in which a
- the device has the advantages that it is a pure membrane process and manages without additional purification of the permeate and / or retentate streams (11) or (8) for many applications.
- Carbon dioxide from methane no pressure swing adsorption or amine scrubbing more for the fine cleaning of the retentate, so that it can be fed into the natural gas grid.
- Retentate (8) and a pure permeate stream (11) are produced in the biogas and natural gas purification. It can therefore be released into the atmosphere without major losses of methane and without much damage to the environment, without that Gas still needs to be further treated by catalytic afterburning or use in one
- inventive method / device according to the invention requires significantly less equipment and energy costs as the known methods of the prior art.
- Permeate component in the feed stream (5) a device or a method can be provided, which is clearly superior to the method of the prior art.
- the device according to the invention or the method according to the invention can be used in particular for the separation of gas mixtures with at least two gases, with very particular preference as the gas mixture a mixture of
- Ratio 50 to 50 could be made.
- Comparative Example 1 Separation of a mixture of methane and carbon dioxide with a mixing ratio of 50 to 50 with a moderately selective polyimide membrane
- Each stage consisted of a hollow fiber membrane module consisting of polyimide hollow fibers from ÜBE (type NM B01 A). 1.78 m 3 / h of a crude gas mixture of 50% methane and 50% carbon dioxide, which corresponds approximately to a gas mixture of biogas, is introduced into a mixing chamber (not shown in Fig. 11) and then together with recycled gas from the gas streams ( 9) and (10) compressed to 25 bar. The compressed and cooled to 20 ° C gas is applied to the feed current separation stage (1). The retentate of the feed stream separation stage (1) is then fed via the first retentate stream (7)
- Retentate separation stage (2) passed.
- a reducing valve (13) on the retentate side of the retentate separation stage (2) is set to 18.2 bara and thus determines the driving force through the membrane of the membrane separation stages (1) and (2).
- the retentate the retentate separation stage (2) has a content of 98.5% methane and 1.5% carbon dioxide. It leave 0.895 m 3 / h this
- Retentate separation stage (2) has a volume flow of 0, 743 m 3 / h with a methane content of 34.5% and a carbon dioxide content of 65.5% and is returned via the second permeate stream (9) in the mixing chamber and from the compressor (4) compressed again.
- the permeate of the feed stream separation stage (1) has a
- Permeate separation stage (3) limited to 4.2 bara. This gives a third permeate stream (11) of permeate separation stage (3) of 0.885 m 3 / h with a composition of 99.0% carbon dioxide and only 1.0% methane.
- the third retentate stream (10) from the permeate separation stage (3) is 0.801 m 3 / h with a
- Crude gas mixture of 50% methane and 50% carbon dioxide which corresponds approximately to a gas mixture of biogas, is introduced into a mixing chamber and then compressed together with recycled gas from the gas streams (9) and (10) to 25 bar.
- the compressed and cooled to 20 ° C gas is on the
- the retentate of this stage is by means of the first retentate stream (7) of the
- Retentate separation stage (2) supplied.
- a reducing valve (13) on the retentate side of the retentate separation stage (2) is set to 18.4 bara and thus determines the driving force through the membrane of the membrane separation stages (1) and (2).
- the retentate of the retentate separation stage (2) has a content of 98.5% methane and 1.5% carbon dioxide. It leave 0.503 m 3 / h of this
- Retentate separation stage (2) has a volume flow of 0.262 m 3 / h with a methane content of 24.6% and a carbon dioxide content of 75.4% and is returned via the second permeate stream (9) in the mixing chamber and from the compressor (4) compressed again.
- the permeate of the feed stream separation stage (1) has a volume flow of 0.547 m 3 / h with a carbon dioxide content of 92.4% and a methane content of 7.6% and is fed via the first permeate stream (6) as feed into the permeate separation stage (3) ,
- the pressure drop across the membrane of stage (1) does not occur to the ambient pressure but is due to a reducing valve (14) on the retentate side of the
- Permeattrenntake (3) limited to 5.0 bara. This gives a third permeate stream (11) from permeate separation stage (3) of 0.497 m 3 / h with a composition of 99.0% carbon dioxide and only 1.0% methane.
- the third retentate stream (10) from the permeate separation stage (3) is 0.050 m 3 / h.
- the sum of recirculated gas streams (9) and (10) is therefore 0.312 m 3 / h or 31.2% based on the supplied amount of gas to be separated. Pure product streams are obtained with a moderate
- Example 2 Separation of a mixture of methane and
- Fig. 11 shown interconnection was used to reduce the concentration of methane in the third permeate stream (11) to below 0.5% by volume.
- Each stage consisted of a hollow fiber membrane module consisting of highly selective polyimide with a separation area of about 5 m 2 per module. These polyimide hollow fibers were according to Example 19 of the Austrian
- Patent application A1164 / 2009 but with a precipitation bath temperature of 40 ° C instead of 10 ° C was worked.
- 1 m 3 / h of a crude gas mixture of 50% methane and 50% carbon dioxide, which corresponds approximately to a gas mixture of biogas is introduced into a mixing chamber and then compressed together with recycled gas from the gas streams (9) and (10) to 25 bar , The compressed and cooled to 20 ° C gas is applied to the feed current separation stage (1)
- the retentate of this stage is produced by means of the first retentate stream (7) of the retentate separation stage (2).
- a reducing valve (13) on the retentate side of the retentate separation stage (2) is set to 18.1 bara and thus determines the driving force through the membrane of the
- Retentate separation stage (2) has a content of 98.5% methane and 1.5% carbon dioxide. 0.555 m 3 / h of this mixture leave the retentate separation stage (2).
- Retentate separation stage (2) has a flow rate of 0.244 m 3 / h with a methane content of 26.1% and a carbon dioxide content of 73.9% and is returned via the second permeate stream (9) in the mixing chamber and from the compressor (4) compressed again.
- the permeate of the feed stream separation stage (1) has a
- Permeattrenncut (3) limited to 4.4 bara. This gives a third permeate stream (11) from permeate separation stage (3) of 0.495 m 3 / h with a composition of 99.5% carbon dioxide and only 0.5% methane.
- the third retentate stream (10) from the permeate separation stage (3) is 0.112 m 3 / h and has a
- composition of 35% methane and 65% carbon dioxide is returned to the mixing chamber and compressed again.
- the sum of recirculated streams (9) and (10) is therefore 0.356m 3 / h or 35.6% based on the amount of gas to be separated. Pure product streams are obtained with a moderate double compression rate.
- the membranes used show a high mixed gas selectivity of carbon dioxide over methane of 45.
- Example 3 Separation of a mixture of methane and
- Fig. 11 shown interconnection supplemented by a vacuum pump, which is not shown in Fig. 11, was used to the concentration of methane in the third
- Permeate stream (11) to less than 0.5 vol.% To reduce. Every level consisted of a hollow fiber membrane module consisting of
- Crude gas mixture of 50% methane and 50% carbon dioxide which corresponds approximately to a gas mixture of biogas, is introduced into a mixing chamber and then compressed together with recycled gas from the gas streams (9) and (10) to 25 bar.
- the compressed and cooled to 20 ° C gas is on the
- the retentate of this stage is by means of the first retentate stream (7) of the
- Retentate separation stage (2) supplied.
- a reducing valve (13) on the retentate side of the retentate separation stage (2) is set to 14.5 bara and thus determines the driving force through the membrane of the membrane separation stages (1) and (2).
- the retentate of the retentate separation stage (2) has a content of 98.5% methane and 1.5% carbon dioxide. It leave 0.505 m 3 / h of this
- Retentate separation stage (2) has a pressure of 0.2 bara
- the gas flow is from the
- the permeate of the feed stream separation stage (1) has a
- Permeattrenncut (3) limited to 4.4 bara. This gives a third permeate stream (11) from permeate separation stage (3) of 0.495 m 3 / h with a composition of 99.5% carbon dioxide and only 0.5% methane.
- the third retentate stream (10) from the permeate separation stage (3) is 0.047 m 3 / h and has a
- Example 4 Separation of a mixture of methane and
- FIG. 11 shows interconnection, supplemented by one
- Vacuum pump which is not shown in Fig. 11, was used to determine the concentration of methane in the second
- Crude gas mixture of 50% methane and 50% carbon dioxide which corresponds approximately to a gas mixture of biogas, is introduced into a mixing chamber and then compressed together with recycled gas from the gas streams (9) and (10) to 25 bar.
- the compressed and cooled to 20 ° C gas is on the
- the retentate of this stage is by means of the first retentate stream (7) of the
- Retentate separation stage (2) supplied.
- a reducing valve (13) on the retentate side of the retentate separation stage (2) is set to 18.1 bara and thus determines the driving force through the membrane of the membrane separation stages (1) and (2).
- the retentate of the retentate separation step (2) has a content of 99.7% methane and 0.3% carbon dioxide. It leave 0.499 m 3 / h this
- Retentate separation stage (2) has a pressure of 0.2 bara
- the gas flow is from the
- the permeate of the feed stream separation stage (1) has a
- Permeattrenncut (3) limited to 4.4 bara. This results in a third permeate stream (11) of permeate separation stage (3) of 0.501 m 3 / h with a composition of 99.5% carbon dioxide and only 0.5% methane.
- the third retentate stream (10) from the permeate separation stage (3) is 0.107 m 3 / h and has a
- Fig. 2 Single-stage membrane separation stage without recycling
- Fig. 3 Single-stage membrane separation stage with recirculation
- Fig. 4 Two-stage membrane separation stage with recompression
- Fig. 5 Retentate and permeate with recompression
- Fig. 7 Permeate step with recompression
- Membrane modules according to the invention Fig. 12 3-stage interconnection of membrane modules with a compressor and retentate recirculation
- Fig.13 3-stage interconnection of membrane modules with one
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Abstract
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Priority Applications (19)
Application Number | Priority Date | Filing Date | Title |
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EA201390039A EA023203B1 (ru) | 2010-07-01 | 2011-05-26 | Способ и установка для разделения газов |
AU2011273795A AU2011273795B2 (en) | 2010-07-01 | 2011-05-26 | Process for separation of gases |
US13/807,831 US8999038B2 (en) | 2010-07-01 | 2011-05-26 | Process for separation of gases |
RS20170479A RS55926B1 (sr) | 2010-07-01 | 2011-05-26 | Postupak za separaciju gasova |
CN2011800321401A CN103068466A (zh) | 2010-07-01 | 2011-05-26 | 分离气体的方法 |
LTEP11722404.8T LT2588217T (lt) | 2010-07-01 | 2011-05-26 | Dujų perskyrimo būdas |
EP11722404.8A EP2588217B1 (de) | 2010-07-01 | 2011-05-26 | Verfahren zur trennung von gasen |
BR112013000082-1A BR112013000082B1 (pt) | 2010-07-01 | 2011-05-26 | Processo de separação de um fluxo de gás bruto |
MX2012014777A MX2012014777A (es) | 2010-07-01 | 2011-05-26 | Proceso para la separacion de gases. |
ES11722404.8T ES2624775T3 (es) | 2010-07-01 | 2011-05-26 | Procedimiento para la separación de gases |
JP2013517129A JP5858992B2 (ja) | 2010-07-01 | 2011-05-26 | ガス分離法 |
KR1020137002616A KR101985551B1 (ko) | 2010-07-01 | 2011-05-26 | 가스의 분리 방법 |
NZ606488A NZ606488A (en) | 2010-07-01 | 2011-05-26 | Process for separation of gases |
CN201610579119.8A CN106039942B (zh) | 2010-07-01 | 2011-05-26 | 分离气体的方法 |
SI201131180A SI2588217T1 (sl) | 2010-07-01 | 2011-05-26 | Postopek ločevanja plinov |
SG2012092193A SG186357A1 (en) | 2010-07-01 | 2011-05-26 | Process for separation of gases |
CA2804233A CA2804233C (en) | 2010-07-01 | 2011-05-26 | Process for separation of gases |
IL223822A IL223822A (en) | 2010-07-01 | 2012-12-24 | Gas separation process |
HRP20170690TT HRP20170690T1 (hr) | 2010-07-01 | 2017-05-10 | Postupak za razdvajanje plinova |
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EP (1) | EP2588217B1 (de) |
JP (1) | JP5858992B2 (de) |
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CN (2) | CN106039942B (de) |
AU (1) | AU2011273795B2 (de) |
BR (1) | BR112013000082B1 (de) |
CA (1) | CA2804233C (de) |
CO (1) | CO6670542A2 (de) |
EA (1) | EA023203B1 (de) |
ES (1) | ES2624775T3 (de) |
HR (1) | HRP20170690T1 (de) |
HU (1) | HUE033254T2 (de) |
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MY (1) | MY165009A (de) |
NZ (1) | NZ606488A (de) |
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