CA2655037A1 - Process for liquefying hydrogen - Google Patents
Process for liquefying hydrogen Download PDFInfo
- Publication number
- CA2655037A1 CA2655037A1 CA002655037A CA2655037A CA2655037A1 CA 2655037 A1 CA2655037 A1 CA 2655037A1 CA 002655037 A CA002655037 A CA 002655037A CA 2655037 A CA2655037 A CA 2655037A CA 2655037 A1 CA2655037 A1 CA 2655037A1
- Authority
- CA
- Canada
- Prior art keywords
- hydrogen
- stream
- precooling
- hydrogen stream
- heat exchange
- 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
Links
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 title claims abstract description 69
- 239000001257 hydrogen Substances 0.000 title claims abstract description 68
- 229910052739 hydrogen Inorganic materials 0.000 title claims abstract description 68
- 238000000034 method Methods 0.000 title claims abstract description 22
- 238000001816 cooling Methods 0.000 claims abstract description 20
- 239000002826 coolant Substances 0.000 claims abstract description 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 20
- 229910052757 nitrogen Inorganic materials 0.000 claims description 10
- 150000002431 hydrogen Chemical class 0.000 claims description 2
- 238000005265 energy consumption Methods 0.000 abstract description 2
- 239000003949 liquefied natural gas Substances 0.000 description 13
- 238000003860 storage Methods 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 6
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 6
- 238000001704 evaporation Methods 0.000 description 5
- 238000000746 purification Methods 0.000 description 5
- 239000003054 catalyst Substances 0.000 description 4
- 230000008020 evaporation Effects 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000003345 natural gas Substances 0.000 description 3
- 239000007789 gas Substances 0.000 description 2
- 238000011109 contamination Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 238000012432 intermediate storage Methods 0.000 description 1
- 230000003137 locomotive effect Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000013404 process transfer Methods 0.000 description 1
- 238000011144 upstream manufacturing Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J1/00—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures
- F25J1/0002—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures characterised by the fluid to be liquefied
- F25J1/0005—Light or noble gases
- F25J1/001—Hydrogen
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J1/00—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures
- F25J1/02—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures requiring the use of refrigeration, e.g. of helium or hydrogen ; Details and kind of the refrigeration system used; Integration with other units or processes; Controlling aspects of the process
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J1/00—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures
- F25J1/003—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures characterised by the kind of cold generation within the liquefaction unit for compensating heat leaks and liquid production
- F25J1/0047—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures characterised by the kind of cold generation within the liquefaction unit for compensating heat leaks and liquid production using an "external" refrigerant stream in a closed vapor compression cycle
- F25J1/0052—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures characterised by the kind of cold generation within the liquefaction unit for compensating heat leaks and liquid production using an "external" refrigerant stream in a closed vapor compression cycle by vaporising a liquid refrigerant stream
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J1/00—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures
- F25J1/006—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures characterised by the refrigerant fluid used
- F25J1/0062—Light or noble gases, mixtures thereof
- F25J1/0067—Hydrogen
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J1/00—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures
- F25J1/006—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures characterised by the refrigerant fluid used
- F25J1/007—Primary atmospheric gases, mixtures thereof
- F25J1/0072—Nitrogen
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J1/00—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures
- F25J1/02—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures requiring the use of refrigeration, e.g. of helium or hydrogen ; Details and kind of the refrigeration system used; Integration with other units or processes; Controlling aspects of the process
- F25J1/0203—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures requiring the use of refrigeration, e.g. of helium or hydrogen ; Details and kind of the refrigeration system used; Integration with other units or processes; Controlling aspects of the process using a single-component refrigerant [SCR] fluid in a closed vapor compression cycle
- F25J1/0205—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures requiring the use of refrigeration, e.g. of helium or hydrogen ; Details and kind of the refrigeration system used; Integration with other units or processes; Controlling aspects of the process using a single-component refrigerant [SCR] fluid in a closed vapor compression cycle as a dual level SCR refrigeration cascade
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J1/00—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures
- F25J1/02—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures requiring the use of refrigeration, e.g. of helium or hydrogen ; Details and kind of the refrigeration system used; Integration with other units or processes; Controlling aspects of the process
- F25J1/0221—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures requiring the use of refrigeration, e.g. of helium or hydrogen ; Details and kind of the refrigeration system used; Integration with other units or processes; Controlling aspects of the process using the cold stored in an external cryogenic component in an open refrigeration loop
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J1/00—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures
- F25J1/02—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures requiring the use of refrigeration, e.g. of helium or hydrogen ; Details and kind of the refrigeration system used; Integration with other units or processes; Controlling aspects of the process
- F25J1/0243—Start-up or control of the process; Details of the apparatus used; Details of the refrigerant compression system used
- F25J1/0257—Construction and layout of liquefaction equipments, e.g. valves, machines
- F25J1/0262—Details of the cold heat exchange system
- F25J1/0264—Arrangement of heat exchanger cores in parallel with different functions, e.g. different cooling streams
- F25J1/0265—Arrangement of heat exchanger cores in parallel with different functions, e.g. different cooling streams comprising cores associated exclusively with the cooling of a refrigerant stream, e.g. for auto-refrigeration or economizer
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J1/00—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures
- F25J1/02—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures requiring the use of refrigeration, e.g. of helium or hydrogen ; Details and kind of the refrigeration system used; Integration with other units or processes; Controlling aspects of the process
- F25J1/0243—Start-up or control of the process; Details of the apparatus used; Details of the refrigerant compression system used
- F25J1/0257—Construction and layout of liquefaction equipments, e.g. valves, machines
- F25J1/0262—Details of the cold heat exchange system
- F25J1/0264—Arrangement of heat exchanger cores in parallel with different functions, e.g. different cooling streams
- F25J1/0265—Arrangement of heat exchanger cores in parallel with different functions, e.g. different cooling streams comprising cores associated exclusively with the cooling of a refrigerant stream, e.g. for auto-refrigeration or economizer
- F25J1/0268—Arrangement of heat exchanger cores in parallel with different functions, e.g. different cooling streams comprising cores associated exclusively with the cooling of a refrigerant stream, e.g. for auto-refrigeration or economizer using a dedicated refrigeration means
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J1/00—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures
- F25J1/02—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures requiring the use of refrigeration, e.g. of helium or hydrogen ; Details and kind of the refrigeration system used; Integration with other units or processes; Controlling aspects of the process
- F25J1/0243—Start-up or control of the process; Details of the apparatus used; Details of the refrigerant compression system used
- F25J1/0279—Compression of refrigerant or internal recycle fluid, e.g. kind of compressor, accumulator, suction drum etc.
- F25J1/0292—Refrigerant compression by cold or cryogenic suction of the refrigerant gas
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J2210/00—Processes characterised by the type or other details of the feed stream
- F25J2210/62—Liquefied natural gas [LNG]; Natural gas liquids [NGL]; Liquefied petroleum gas [LPG]
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J2240/00—Processes or apparatus involving steps for expanding of process streams
- F25J2240/60—Expansion by ejector or injector, e.g. "Gasstrahlpumpe", "venturi mixing", "jet pumps"
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J2245/00—Processes or apparatus involving steps for recycling of process streams
- F25J2245/90—Processes or apparatus involving steps for recycling of process streams the recycled stream being boil-off gas from storage
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J2270/00—Refrigeration techniques used
- F25J2270/90—External refrigeration, e.g. conventional closed-loop mechanical refrigeration unit using Freon or NH3, unspecified external refrigeration
- F25J2270/904—External refrigeration, e.g. conventional closed-loop mechanical refrigeration unit using Freon or NH3, unspecified external refrigeration by liquid or gaseous cryogen in an open loop
Abstract
The invention relates to a process for liquefying hydrogen. To reduce the specific energy consumption, the following process steps are used: a) the precooling of the hydrogen stream by indirect heat exchange against a pressurized LNG stream to a temperature of between 140 and 130 K, b) the precooling of the hydrogen stream by indirect heat exchange against a coolant to a temperature of between 85 and 75 K, c) where the precooling of the coolant takes place against a pressurized LNG stream, and d) the cooling and at least partial liquefaction of the precooled hydrogen stream takes place by indirect heat exchange against another hydrogen stream channeled through a closed cooling circuit, e) where the precooling of the condensed hydrogen stream, which is channeled through a closed cooling circuit, takes place against a pressurized LNG stream.
Description
PROCESS FOR LIQUEFYING HYDROGEN
DESCRIPTION
The invention relates to a method for liquefying hydrogen.
Hydrogen in particular is currently increasingly gaining in importance as energy carrier due to the growing energy demand and increased environmental consciousness. Trucks, buses, passenger cars and locomotives are thus already powered by means of engines which are operated by natural gas or hydrogen as well as by means of combinations of fuel cell and electric motor. In those cases, the most sensible form of storage of the hydrogen "on board" the aforementioned means of transportation is the liquid form. Even though, for this purpose, the hydrogen must be cooled to approximately 25 K and maintained at this temperature - which is only achievable by using appropriate insulation measures on the storage containers or storage tanks -, owing to the low density of GH2, storage in gaseous form in the aforementioned means of transportation is, as a rule, less favorable, since, in this case, storage has to take place in large-volume and heavy storage tanks under high pressures.
Hydrogen liquefaction processes normally comprise two process steps, namely the so-called precooling step as well as the subsequent liquefaction step. In the above processes, hydrogen must be cooled to below its upper Joule-Thomson inversion temperature - this is understood to be the temperature below which an expanding gas cools down - before it can be liauefied.
The hydrogen must therefore usually be precooled to a tem-cerature of at least -1500C before it can be supplied to the subsequent liquefaction process.
Gaseous hydrogen is usually composed of approximately 750 ortho-hydrogen and approximately 2501 para-hydrogen.
For this reason, during the liquefaction process -since the liquefied hydrogen is normally to be intermediately stored over a longer period of time -, the ortho-hydrogen must be converted into para-hydrogen. Typically, a proportion of at least 990 para-hydrogen is aimed for. If such a conversion is not performed, a quicker evaporation of the liquefied hydrogen will be the result. The conversion from ortho-hydrogen to para-hydrogen takes place by means of suitable conversion catalysts.
A large number of methods for liquefying hydrogen are known from the literature, in which the precooling of the gaseous hydrogen takes place against a coolant circuit or coolant mixture circuit. Nitrogen is often used as coolant in this case. Hydrogen liquefaction methods are known from the international patent application WO 2005/080892 as well as from the European patent application 1 580 506, where the precooling of the hydrogen stream to be liquefied takes place in indirect heat exchange with a pressurized LNG (Liquid Natural Gas) stream. The LNG evaporating during this process transfers its cold to the gaseous hydrogen stream to be precooled. The evaporation of LNG is an issue in particular in LNG terminals. This evaporation normally takes place by means of suitable natural gas burners which are immersed in water baths and are operated with a small partial stream of the LNG.
It is the object of the present invention to provide a method for liquefying hydrogen, which, WO 2007/144078 PCT/Ea2007/004902 compared to the methods which form part of the state of the art, has a lower specific energy consumption.
The method according to the invention for liquefying hydrogen comprises the following method steps:
a) precooling of the hydrogen stream by indirect heat exchange against a pressurized LNG stream to a temperature of between 140 and 130 K, b) precooling of the hydrogen stream by indirect heat exchange against a coolant to a temperature of between 85 and 75 K, C) with the precooling of the coolant taking place against a pressurized LNG stream, and d) cooling and at least partial liquefaction of the precooled hydrogen stream by indirect heat exchange against a further hydrogen stream which is circulated in a closed cooling circuit, e) with the precooling of the compressed hydrogen stream, which is circulated in a closed cooling circuit, taking place against a pressurized LNG
stream.
The method according to the invention for liquefying hydrogen will be explained in more detail below with reference to the exemplary embodiment illustrated in the figure.
The hydrogen stream to be liquefied is supplied via line 1 with a pressure of 2200 kPa and a temperature of 300 K to the heat exchanger El. In the latter, the hydrogen stream is cooled to a temperature of 135 K
against an LNG stream, which is conducted via line A
through the heat exchanger El and has a temperature of 125 K and a pressure of 7800 kPa.
w0 2007/144078 PCT/EP2007/004902 It should be emphasized that all of the heat exchangers shown in the figure represent in each case one or also more, if necessary different heat exchangers or heat exchanger types.
The precooled hydrogen stream is now supplied via line 2 to a further heat exchanger E2 and cooled therein to a temperature of 80 K against a nitrogen cooling circuit, which will be described in more detail below.
The hydrogen stream precooled to 80 K is subsequently supplied via line 3 to a purification device 4 working preferably adsorptively, in which final traces of contamination are removed from the hydrogen stream to be liquefied. The purification device 4 usually comprises at least two adsorbers arranged in parallel so that a continuous purification process can be realized by switching.
The hydrogen stream to be liquefied withdrawn from the purification device 4 via line 5 is supplied to the heat exchanger E4 and cooled therein against the still to be described closed hydrogen cooling circuit to a temperature of 26 K. A pressure reduction to approximately 200 kPa takes place in the expansion device 8 downstream of the heat exchanger E4, which results in a partial liquefaction of the cooled hydrogen stream. Subsequent to the completed liquefaction of the gas phase in the heat exchanger E7, a liquid hydrogen product stream is withdrawn via line 9 and supplied to its further use and/or intermediate storage.
Alternatively, the expansion device 8 can also be realized by a combination consisting of an expansion valve and an ejector following the expansion valve. In = s case, ~asaous hydrogen produced during the intermediat~ storage of the liquid hvdrogen product stream can be supplied to the ejector.
S The open hydrogen cooling circuit is composed of the line sections 17, 11, 13, 15 and 16, the heat exchangers E4, E5, E6 und E7, at least one expansion device 12, and a preferably multi-stage compressor 14.
Hydrogen is first supplied via line 17 to the heat exchanger E4 and cooled therein. It is subsequently supplied via line 11 to the expansion device 12 and expanded in it for the purpose of providing the peak cold necessary for the liquefaction of the hydrogen.
Next, the evaporation takes place in the heat exchanger E7 and a heating of the expanded hydrogen stream in the heat exchanger E4 in indirect heat exchange with the hydrogen stream to be cooled and liquefied in line 17.
The heated hydrogen stream is supplied via line 13 to the heat exchanger ES and heated against itself therein, prior to being compressed to the desired circuit pressure in the compressor unit 14.
The compressed hydrogen stream is supplied via line 15 to a heat exchanger E6 and cooled therein against a further partial LNG stream, which is supplied to the heat exchanger E6 via line C. This cooled hydrogen stream is subsequently supplied via line 16 to the heat exchanger E5, cooled against itself therein and thereafter supplied again via the line sections 17 to the already described heat exchanger E4.
For reasons of clarity, several expansion devices are not shown in the figure; they are being supplied in each case with cooled partial hydrogen streams from the line sections 17 and 11 and, subsequent to the WO 2007/144078 = PCT/EP2007/004902 completed cooling expansion, supplied again to the cooling circuit 13 shown, located upstream of the expansion device 12 (before and/or after E4).
5?'he aforementioned nitrogen cooling circuit used for precooling the natural gas stream to be liquefied by means of the heat exchanger E2, has in addition to the line regions 20, 21, 23 and 24 a further heat exchanger E3, an expansion device 25, as well as a preferably multi-stage compressor unit 22.
The nitrogen stream expanded in the expansion device 25 and having a cooling effect in the process is supplied via line 20 to the aforementioned heat exchanger E2 and heated therein against the hydrogen stream to be cooled, and evaporated. The evaporated nitrogen stream is then supplied via line 21 to the compressor unit 22 and compressed therein to the desired circuit pressure.
The compressed nitrogen stream is supplied via line 23 to the heat exchanger E3 and cooled therein against a further LNG stream, which is supplied to the heat exchanger E3 via line B. The cooled nitrogen stream is then supplied via line 24 to the aforementioned expansion device 25.
According to the invention, the LNG being available in the hydrogen liquefaction process environment is now used for precooling the hydrogen stream to be liquefied (heat exchanger El), for cooling the compressed nitrogen in the nitrogen cooling circuit (heat exchanger E3), as well as for cooling the compressed hydrogen stream (heat exchanger E6) circulating in the open hydrogen cooling circuit.
For reasons of clarity, the catalysts and/or catalyst mountings required for the desired or possibly required V70 2007/144078 PCT/E.P2007/004902 ortho-para conversion of the hydrogen are not shown ir_ the figure. Generally, a first ortho-para conversion will be provided downstream of the purification device 4. In this -jurification device 4, an increase of the para-hydrogen content from approximately 25 to approximately 43% can take place. The following ortho-para conversion takes place preferably by way of catalysts arranged in the passages of the heat exchanger E4. Preferably, the liquid hydrogen product stream withdrawn via line 9 should consist of at least 9901 para-hydrogen.
DESCRIPTION
The invention relates to a method for liquefying hydrogen.
Hydrogen in particular is currently increasingly gaining in importance as energy carrier due to the growing energy demand and increased environmental consciousness. Trucks, buses, passenger cars and locomotives are thus already powered by means of engines which are operated by natural gas or hydrogen as well as by means of combinations of fuel cell and electric motor. In those cases, the most sensible form of storage of the hydrogen "on board" the aforementioned means of transportation is the liquid form. Even though, for this purpose, the hydrogen must be cooled to approximately 25 K and maintained at this temperature - which is only achievable by using appropriate insulation measures on the storage containers or storage tanks -, owing to the low density of GH2, storage in gaseous form in the aforementioned means of transportation is, as a rule, less favorable, since, in this case, storage has to take place in large-volume and heavy storage tanks under high pressures.
Hydrogen liquefaction processes normally comprise two process steps, namely the so-called precooling step as well as the subsequent liquefaction step. In the above processes, hydrogen must be cooled to below its upper Joule-Thomson inversion temperature - this is understood to be the temperature below which an expanding gas cools down - before it can be liauefied.
The hydrogen must therefore usually be precooled to a tem-cerature of at least -1500C before it can be supplied to the subsequent liquefaction process.
Gaseous hydrogen is usually composed of approximately 750 ortho-hydrogen and approximately 2501 para-hydrogen.
For this reason, during the liquefaction process -since the liquefied hydrogen is normally to be intermediately stored over a longer period of time -, the ortho-hydrogen must be converted into para-hydrogen. Typically, a proportion of at least 990 para-hydrogen is aimed for. If such a conversion is not performed, a quicker evaporation of the liquefied hydrogen will be the result. The conversion from ortho-hydrogen to para-hydrogen takes place by means of suitable conversion catalysts.
A large number of methods for liquefying hydrogen are known from the literature, in which the precooling of the gaseous hydrogen takes place against a coolant circuit or coolant mixture circuit. Nitrogen is often used as coolant in this case. Hydrogen liquefaction methods are known from the international patent application WO 2005/080892 as well as from the European patent application 1 580 506, where the precooling of the hydrogen stream to be liquefied takes place in indirect heat exchange with a pressurized LNG (Liquid Natural Gas) stream. The LNG evaporating during this process transfers its cold to the gaseous hydrogen stream to be precooled. The evaporation of LNG is an issue in particular in LNG terminals. This evaporation normally takes place by means of suitable natural gas burners which are immersed in water baths and are operated with a small partial stream of the LNG.
It is the object of the present invention to provide a method for liquefying hydrogen, which, WO 2007/144078 PCT/Ea2007/004902 compared to the methods which form part of the state of the art, has a lower specific energy consumption.
The method according to the invention for liquefying hydrogen comprises the following method steps:
a) precooling of the hydrogen stream by indirect heat exchange against a pressurized LNG stream to a temperature of between 140 and 130 K, b) precooling of the hydrogen stream by indirect heat exchange against a coolant to a temperature of between 85 and 75 K, C) with the precooling of the coolant taking place against a pressurized LNG stream, and d) cooling and at least partial liquefaction of the precooled hydrogen stream by indirect heat exchange against a further hydrogen stream which is circulated in a closed cooling circuit, e) with the precooling of the compressed hydrogen stream, which is circulated in a closed cooling circuit, taking place against a pressurized LNG
stream.
The method according to the invention for liquefying hydrogen will be explained in more detail below with reference to the exemplary embodiment illustrated in the figure.
The hydrogen stream to be liquefied is supplied via line 1 with a pressure of 2200 kPa and a temperature of 300 K to the heat exchanger El. In the latter, the hydrogen stream is cooled to a temperature of 135 K
against an LNG stream, which is conducted via line A
through the heat exchanger El and has a temperature of 125 K and a pressure of 7800 kPa.
w0 2007/144078 PCT/EP2007/004902 It should be emphasized that all of the heat exchangers shown in the figure represent in each case one or also more, if necessary different heat exchangers or heat exchanger types.
The precooled hydrogen stream is now supplied via line 2 to a further heat exchanger E2 and cooled therein to a temperature of 80 K against a nitrogen cooling circuit, which will be described in more detail below.
The hydrogen stream precooled to 80 K is subsequently supplied via line 3 to a purification device 4 working preferably adsorptively, in which final traces of contamination are removed from the hydrogen stream to be liquefied. The purification device 4 usually comprises at least two adsorbers arranged in parallel so that a continuous purification process can be realized by switching.
The hydrogen stream to be liquefied withdrawn from the purification device 4 via line 5 is supplied to the heat exchanger E4 and cooled therein against the still to be described closed hydrogen cooling circuit to a temperature of 26 K. A pressure reduction to approximately 200 kPa takes place in the expansion device 8 downstream of the heat exchanger E4, which results in a partial liquefaction of the cooled hydrogen stream. Subsequent to the completed liquefaction of the gas phase in the heat exchanger E7, a liquid hydrogen product stream is withdrawn via line 9 and supplied to its further use and/or intermediate storage.
Alternatively, the expansion device 8 can also be realized by a combination consisting of an expansion valve and an ejector following the expansion valve. In = s case, ~asaous hydrogen produced during the intermediat~ storage of the liquid hvdrogen product stream can be supplied to the ejector.
S The open hydrogen cooling circuit is composed of the line sections 17, 11, 13, 15 and 16, the heat exchangers E4, E5, E6 und E7, at least one expansion device 12, and a preferably multi-stage compressor 14.
Hydrogen is first supplied via line 17 to the heat exchanger E4 and cooled therein. It is subsequently supplied via line 11 to the expansion device 12 and expanded in it for the purpose of providing the peak cold necessary for the liquefaction of the hydrogen.
Next, the evaporation takes place in the heat exchanger E7 and a heating of the expanded hydrogen stream in the heat exchanger E4 in indirect heat exchange with the hydrogen stream to be cooled and liquefied in line 17.
The heated hydrogen stream is supplied via line 13 to the heat exchanger ES and heated against itself therein, prior to being compressed to the desired circuit pressure in the compressor unit 14.
The compressed hydrogen stream is supplied via line 15 to a heat exchanger E6 and cooled therein against a further partial LNG stream, which is supplied to the heat exchanger E6 via line C. This cooled hydrogen stream is subsequently supplied via line 16 to the heat exchanger E5, cooled against itself therein and thereafter supplied again via the line sections 17 to the already described heat exchanger E4.
For reasons of clarity, several expansion devices are not shown in the figure; they are being supplied in each case with cooled partial hydrogen streams from the line sections 17 and 11 and, subsequent to the WO 2007/144078 = PCT/EP2007/004902 completed cooling expansion, supplied again to the cooling circuit 13 shown, located upstream of the expansion device 12 (before and/or after E4).
5?'he aforementioned nitrogen cooling circuit used for precooling the natural gas stream to be liquefied by means of the heat exchanger E2, has in addition to the line regions 20, 21, 23 and 24 a further heat exchanger E3, an expansion device 25, as well as a preferably multi-stage compressor unit 22.
The nitrogen stream expanded in the expansion device 25 and having a cooling effect in the process is supplied via line 20 to the aforementioned heat exchanger E2 and heated therein against the hydrogen stream to be cooled, and evaporated. The evaporated nitrogen stream is then supplied via line 21 to the compressor unit 22 and compressed therein to the desired circuit pressure.
The compressed nitrogen stream is supplied via line 23 to the heat exchanger E3 and cooled therein against a further LNG stream, which is supplied to the heat exchanger E3 via line B. The cooled nitrogen stream is then supplied via line 24 to the aforementioned expansion device 25.
According to the invention, the LNG being available in the hydrogen liquefaction process environment is now used for precooling the hydrogen stream to be liquefied (heat exchanger El), for cooling the compressed nitrogen in the nitrogen cooling circuit (heat exchanger E3), as well as for cooling the compressed hydrogen stream (heat exchanger E6) circulating in the open hydrogen cooling circuit.
For reasons of clarity, the catalysts and/or catalyst mountings required for the desired or possibly required V70 2007/144078 PCT/E.P2007/004902 ortho-para conversion of the hydrogen are not shown ir_ the figure. Generally, a first ortho-para conversion will be provided downstream of the purification device 4. In this -jurification device 4, an increase of the para-hydrogen content from approximately 25 to approximately 43% can take place. The following ortho-para conversion takes place preferably by way of catalysts arranged in the passages of the heat exchanger E4. Preferably, the liquid hydrogen product stream withdrawn via line 9 should consist of at least 9901 para-hydrogen.
Claims (2)
1. A method for liquefying hydrogen, comprising the following method steps:
a) precooling of the hydrogen stream by indirect heat exchange against a pressurized LNG stream to a temperature of between 140 and 130 K, b) precooling of the hydrogen stream by indirect heat exchange against a coolant to a temperature of between 85 and 75 K, c) with the precooling of the coolant taking place against a pressurized LNG stream, and d) cooling and at least partial liquefaction of the precooled hydrogen stream by indirect heat exchange against a further hydrogen stream which is circulated in a closed cooling circuit, e) with the precooling of the compressed hydrogen stream, which is circulated in a closed cooling circuit, taking place against a pressurized LNG stream.
a) precooling of the hydrogen stream by indirect heat exchange against a pressurized LNG stream to a temperature of between 140 and 130 K, b) precooling of the hydrogen stream by indirect heat exchange against a coolant to a temperature of between 85 and 75 K, c) with the precooling of the coolant taking place against a pressurized LNG stream, and d) cooling and at least partial liquefaction of the precooled hydrogen stream by indirect heat exchange against a further hydrogen stream which is circulated in a closed cooling circuit, e) with the precooling of the compressed hydrogen stream, which is circulated in a closed cooling circuit, taking place against a pressurized LNG stream.
2. The method as claimed in claim 1, characterized in that nitrogen is used as coolant for the precooling of the hydrogen stream.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102006027199.8 | 2006-06-12 | ||
DE102006027199A DE102006027199A1 (en) | 2006-06-12 | 2006-06-12 | Process for liquefying hydrogen |
PCT/EP2007/004902 WO2007144078A2 (en) | 2006-06-12 | 2007-06-01 | Process for liquefying hydrogen |
Publications (1)
Publication Number | Publication Date |
---|---|
CA2655037A1 true CA2655037A1 (en) | 2007-12-21 |
Family
ID=38663834
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002655037A Abandoned CA2655037A1 (en) | 2006-06-12 | 2007-06-01 | Process for liquefying hydrogen |
Country Status (9)
Country | Link |
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US (1) | US20100083695A1 (en) |
EP (1) | EP2027423A2 (en) |
JP (1) | JP2009540259A (en) |
KR (1) | KR20090016515A (en) |
CN (1) | CN101466990A (en) |
CA (1) | CA2655037A1 (en) |
DE (1) | DE102006027199A1 (en) |
RU (1) | RU2009100154A (en) |
WO (1) | WO2007144078A2 (en) |
Families Citing this family (20)
Publication number | Priority date | Publication date | Assignee | Title |
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CN102080919B (en) * | 2011-01-18 | 2013-08-07 | 四川亚联高科技股份有限公司 | Hydrogen liquefaction process |
JP5783945B2 (en) * | 2012-03-30 | 2015-09-24 | 大陽日酸株式会社 | Liquefaction device and starting method thereof |
GB2512360B (en) | 2013-03-27 | 2015-08-05 | Highview Entpr Ltd | Method and apparatus in a cryogenic liquefaction process |
KR101458098B1 (en) * | 2013-06-26 | 2014-11-05 | 한국과학기술연구원 | A pre-cooler for hydrogen liquefying apparatus |
EP3162871A1 (en) * | 2015-10-27 | 2017-05-03 | Linde Aktiengesellschaft | Hydrogen-neon mixture refrigeration cycle for large-scale hydrogen cooling and liquefaction |
EP3163235A1 (en) * | 2015-10-27 | 2017-05-03 | Linde Aktiengesellschaft | Novel cascade process for cooling and liquefying hydrogen in large-scale |
EP3163236A1 (en) * | 2015-10-27 | 2017-05-03 | Linde Aktiengesellschaft | Large-scale hydrogen liquefaction by means of a high pressure hydrogen refrigeration cycle combined to a novel single mixed-refrigerant precooling |
RU2713556C1 (en) * | 2016-03-10 | 2020-02-05 | ДжГК Корпорейшн | New production equipment and method of producing liquefied hydrogen and liquefied natural gas |
US10634425B2 (en) * | 2016-08-05 | 2020-04-28 | L'air Liquide, Societe Anonyme Pour L'etude Et L'exploitation Des Procedes Georges Claude | Integration of industrial gas site with liquid hydrogen production |
CN106352656B (en) * | 2016-08-23 | 2018-10-09 | 杭州福斯达深冷装备股份有限公司 | It is a kind of with the devices and methods therefor of liquid nitrogen washing ammonia synthesis gas coproduction LNG |
KR20200109054A (en) * | 2019-03-12 | 2020-09-22 | 주식회사 한국초저온 | Apparatus for hydrogen liquefaction using cold energy of liquid natural gas |
KR102267677B1 (en) | 2019-10-22 | 2021-06-22 | 고등기술연구원연구조합 | System for cold heat transfer and hydrogen liquefaction using cold heat circulation of liguified hydrogen |
US20210131725A1 (en) * | 2019-10-31 | 2021-05-06 | Hylium Industries, Inc. | Hydrogen liquefaction system |
KR102328753B1 (en) * | 2019-12-02 | 2021-11-18 | 한국기계연구원 | Hydrogen liquefying apparatus and hydrogen liquefying process |
KR102470782B1 (en) * | 2020-08-19 | 2022-11-28 | 고등기술연구원연구조합 | Hydrogen Liquefaction System and Method |
CN112557577A (en) * | 2020-10-22 | 2021-03-26 | 合肥综合性国家科学中心能源研究院(安徽省能源实验室) | System for testing dynamic performance of catalytic conversion of para-hydrogen |
KR102373686B1 (en) | 2020-12-23 | 2022-03-15 | 주식회사 헥사 | Pre-cooling module of hydrogen and hydrogen liquefier containing thereof |
FR3123422B1 (en) * | 2021-05-31 | 2024-01-19 | Engie | DEVICE AND METHOD FOR COOLING A FLOW OF A TARGET FLUID TO A TEMPERATURE LESS OR EQUAL TO 90 K |
FR3132566B1 (en) | 2022-02-04 | 2024-03-08 | Air Liquide | Method and apparatus for cooling carbon dioxide and hydrogen |
CN117168087A (en) * | 2022-05-25 | 2023-12-05 | 上海司氢科技有限公司 | Modular hydrogen liquefaction system |
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BE573733A (en) * | 1957-12-11 | 1900-01-01 | ||
US3398545A (en) * | 1965-03-19 | 1968-08-27 | Conch Int Methane Ltd | Hydrogen recovery from a refinery tail gas employing two stage scrubbing |
US3347055A (en) * | 1965-03-26 | 1967-10-17 | Air Reduction | Method for recuperating refrigeration |
US4090361A (en) * | 1976-03-15 | 1978-05-23 | Terry Lynn E | Power cycles based upon cyclical hydriding and dehydriding of a material |
GB2142423B (en) * | 1983-03-10 | 1986-08-06 | Smith Dr Eric Murray | Production of liquid hydrogen |
JPS61140777A (en) * | 1984-12-11 | 1986-06-27 | 株式会社神戸製鋼所 | Manufacture of liquid h2 and gas natural gas |
JPH0448184A (en) * | 1990-06-13 | 1992-02-18 | Tokyo Gas Co Ltd | Manufacture of liquid hydrogen |
FR2723183B1 (en) * | 1994-07-29 | 1997-01-10 | Grenier Maurice | HYDROGEN LIQUEFACTION PROCESS AND PLANT |
JP3647028B2 (en) * | 2001-02-19 | 2005-05-11 | 日本エア・リキード株式会社 | Liquid hydrogen production method and liquid hydrogen production equipment |
JP4429552B2 (en) * | 2001-07-16 | 2010-03-10 | 関西電力株式会社 | Liquid hydrogen production system |
JP2004210597A (en) * | 2003-01-06 | 2004-07-29 | Toshiba Corp | Waste-heat-using hydrogen/oxygen system and method for producing liquid hydrogen |
JP4217656B2 (en) * | 2004-01-27 | 2009-02-04 | 関西電力株式会社 | Hydrogen liquefier and liquid hydrogen production system |
WO2005080892A1 (en) * | 2004-02-23 | 2005-09-01 | Shell Internationale Research Maatschappij B.V. | Liquefying hydrogen |
GB0406615D0 (en) * | 2004-03-24 | 2004-04-28 | Air Prod & Chem | Process and apparatus for liquefying hydrogen |
-
2006
- 2006-06-12 DE DE102006027199A patent/DE102006027199A1/en not_active Withdrawn
-
2007
- 2007-06-01 KR KR1020097000481A patent/KR20090016515A/en not_active Application Discontinuation
- 2007-06-01 JP JP2009514659A patent/JP2009540259A/en active Pending
- 2007-06-01 CA CA002655037A patent/CA2655037A1/en not_active Abandoned
- 2007-06-01 US US12/304,357 patent/US20100083695A1/en not_active Abandoned
- 2007-06-01 EP EP07725781A patent/EP2027423A2/en not_active Withdrawn
- 2007-06-01 WO PCT/EP2007/004902 patent/WO2007144078A2/en active Application Filing
- 2007-06-01 RU RU2009100154/06A patent/RU2009100154A/en not_active Application Discontinuation
- 2007-06-01 CN CNA2007800220692A patent/CN101466990A/en active Pending
Also Published As
Publication number | Publication date |
---|---|
US20100083695A1 (en) | 2010-04-08 |
EP2027423A2 (en) | 2009-02-25 |
KR20090016515A (en) | 2009-02-13 |
RU2009100154A (en) | 2010-07-20 |
WO2007144078A2 (en) | 2007-12-21 |
WO2007144078A3 (en) | 2008-01-17 |
JP2009540259A (en) | 2009-11-19 |
DE102006027199A1 (en) | 2007-12-13 |
CN101466990A (en) | 2009-06-24 |
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