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WO2013001753A1 - Hydrogen generation device and fuel cell system - Google Patents

Hydrogen generation device and fuel cell system Download PDF

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Publication number
WO2013001753A1
WO2013001753A1 PCT/JP2012/004017 JP2012004017W WO2013001753A1 WO 2013001753 A1 WO2013001753 A1 WO 2013001753A1 JP 2012004017 W JP2012004017 W JP 2012004017W WO 2013001753 A1 WO2013001753 A1 WO 2013001753A1
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WIPO (PCT)
Prior art keywords
raw material
pressure
reformer
gas
flow path
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PCT/JP2012/004017
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French (fr)
Japanese (ja)
Inventor
佳央 田村
浩一 楠村
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Panasonic Corp
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Panasonic Corp
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Publication date
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    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B3/00Hydrogen; Gaseous mixtures containing hydrogen; Separation of hydrogen from mixtures containing it; Purification of hydrogen
    • C01B3/02Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen
    • C01B3/32Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air
    • C01B3/34Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air by reaction of hydrocarbons with gasifying agents
    • C01B3/38Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air by reaction of hydrocarbons with gasifying agents using catalysts
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00Fuel cells; Manufacture thereof
    • H01M8/04Auxiliary arrangements, e.g. for control of pressure or for circulation of fluids
    • H01M8/04298Processes for controlling fuel cells or fuel cell systems
    • H01M8/04694Processes for controlling fuel cells or fuel cell systems characterised by variables to be controlled
    • H01M8/04746Pressure; Flow
    • H01M8/04776Pressure; Flow at auxiliary devices, e.g. reformer, compressor, burner
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00Fuel cells; Manufacture thereof
    • H01M8/06Combination of fuel cells with means for production of reactants or for treatment of residues
    • H01M8/0606Combination of fuel cells with means for production of reactants or for treatment of residues with means for production of gaseous reactants
    • H01M8/0612Combination of fuel cells with means for production of reactants or for treatment of residues with means for production of gaseous reactants from carbon-containing material
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00Fuel cells; Manufacture thereof
    • H01M8/06Combination of fuel cells with means for production of reactants or for treatment of residues
    • H01M8/0662Treatment of gaseous reactants or gaseous residues, e.g. cleaning
    • H01M8/0675Removal of sulfur
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/10Catalysts for performing the hydrogen forming reactions
    • C01B2203/1041Composition of the catalyst
    • C01B2203/1047Group VIII metal catalysts
    • C01B2203/1052Nickel or cobalt catalysts
    • C01B2203/1058Nickel catalysts
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/10Catalysts for performing the hydrogen forming reactions
    • C01B2203/1041Composition of the catalyst
    • C01B2203/1047Group VIII metal catalysts
    • C01B2203/1064Platinum group metal catalysts
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/12Feeding the process for making hydrogen or synthesis gas
    • C01B2203/1205Composition of the feed
    • C01B2203/1211Organic compounds or organic mixtures used in the process for making hydrogen or synthesis gas
    • C01B2203/1235Hydrocarbons
    • C01B2203/1241Natural gas or methane
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/30Hydrogen technology
    • Y02E60/50Fuel cells

Definitions

  • the present invention relates to a hydrogen generator, a fuel cell system, and an operation method thereof. More specifically, the present invention relates to a hydrogen generator equipped with a hydrodesulfurizer that removes sulfur compounds in a raw material gas, and a fuel cell system.
  • the supply source of hydrogen gas as fuel for power generation is not maintained as a general infrastructure. Therefore, for example, a hydrogen generator that uses a source gas supplied from an existing infrastructure such as city gas or propane gas and generates a hydrogen-containing gas by a reforming reaction between the source gas and water is additionally provided.
  • the hydrogen generator is a reformer that reforms the raw material gas and water, a gas-shift-reaction converter that converts carbon monoxide and water vapor, and carbon monoxide, mainly air.
  • a configuration is provided in which a CO remover that is oxidized with an oxidizing gas is provided.
  • a catalyst suitable for each reaction is used.
  • a Ru catalyst or Ni catalyst is used for the reformer
  • a Cu—Zn catalyst is used for the shifter
  • a Ru catalyst is used for the CO remover. Yes.
  • Each reactor has a suitable temperature.
  • the reformer is often used at about 600 to 700 ° C.
  • the transformer is used at about 350 to 200 ° C.
  • the CO remover is used at about 200 to 100 ° C. in many cases.
  • electrode poisoning due to carbon monoxide tends to occur. For this reason, it is necessary to suppress the carbon monoxide concentration in the supplied hydrogen-containing gas to several tens of ppm by volume or less.
  • the CO remover reduces the carbon monoxide concentration by oxidizing carbon monoxide.
  • source gases such as city gas contain sulfur compounds. Since the sulfur compound is a poisoning substance for the reforming catalyst, it must be removed by some method.
  • Hydrogen generators have been proposed that employ a method of removing by room temperature adsorption (see, for example, Patent Document 1) or a method of removing by hydrodesulfurization using hydrogen (see, for example, Patent Document 2).
  • Room temperature adsorptive desulfurization is easy to handle because it does not require heating and hydrogen, but the desulfurization capacity is not large.
  • Hydrodesulfurization requires heating and hydrogen and is not easy to handle, but has a feature of large desulfurization capacity.
  • a hydrogen generation apparatus that uses room temperature adsorptive desulfurization at start-up and switches to hydrodesulfurization after hydrogen can be generated has also been proposed (see, for example, Patent Documents 2 and 3).
  • a hydrogen-containing gas is supplied to a raw material supplied to the hydrodesulfurizer via a recycle channel branched from a channel through which the hydrogen-containing gas that has passed through the reformer flows. It is comprised so that.
  • JP 2004-228016 A Japanese Patent Laid-Open No. 1-275697 Japanese Patent No. 4264791 JP-A-8-293315
  • the present invention solves the above-mentioned problem, and even when the supply pressure of the raw material gas is high, a hydrogen generator and fuel in which a decrease in the flow rate of hydrogen gas flowing through the recycle channel is suppressed as compared with a conventional hydrogen generator It is an object to provide a battery and a method for operating the battery.
  • the present inventors have intensively studied in a hydrogen generator that employs hydrodesulfurization. As a result, the following knowledge was obtained.
  • the pressure regulator and the booster are arranged in this order with respect to the flow direction of the raw material gas, and downstream of the recycling flow path. Connect the end to the raw material flow path from the pressure regulator to the booster. Then, even if the supply pressure of the raw material gas is high, the pressure is reduced by the pressure regulator, so that a reduction in the differential pressure between the upstream end and the downstream end of the recycle channel is suppressed.
  • the hydrogen generator of the present invention includes a reformer that generates a hydrogen-containing gas from a raw material gas, a raw material channel through which the raw material gas supplied to the reformer flows, and the raw material
  • a pressure regulator provided in the flow path for reducing the pressure of the raw material gas
  • a booster provided in the raw material flow path for raising the pressure of the raw material gas that has passed through the pressure regulator; and provided in the raw material flow path.
  • a hydrodesulfurizer that removes sulfur compounds in the raw material gas that has passed through the pressure regulator, and a hydrogen-containing gas generated in the reformer downstream of the pressure regulator and the hydrodesulfurizer, and And a recycle flow path for supplying the raw material flow path upstream of the booster.
  • the fuel cell system of the present invention includes the hydrogen generator and a fuel cell that generates power using a hydrogen-containing gas supplied from the hydrogen generator.
  • the hydrogen generation device and the fuel cell system of the present invention even if the supply pressure of the raw material gas is high, a decrease in the flow rate of the hydrogen gas flowing through the recycle channel is suppressed as compared with the conventional hydrogen generation device.
  • FIG. 1 is a block diagram illustrating an example of a schematic configuration of a hydrogen generator according to the first embodiment.
  • FIG. 2 is a block diagram illustrating an example of a schematic configuration of the hydrogen generator according to the second embodiment.
  • FIG. 3 is a block diagram illustrating an example of a schematic configuration of the hydrogen generator according to the third embodiment.
  • FIG. 4 is a block diagram illustrating an example of a schematic configuration of the hydrogen generator according to the fourth embodiment.
  • FIG. 5 is a flowchart illustrating an example of an operation method of the hydrogen generator according to the fourth embodiment.
  • FIG. 6 is a block diagram illustrating an example of a schematic configuration of a fuel cell system according to a modification of the fourth embodiment.
  • FIG. 7 is a block diagram illustrating an example of a schematic configuration of a fuel cell system according to the fifth embodiment.
  • FIG. 8 is a block diagram illustrating an example of a schematic configuration of a fuel cell system according to a modification of the fifth embodiment.
  • the hydrogen generator of the first embodiment includes a reformer that generates a hydrogen-containing gas from a raw material gas, a raw material channel through which the raw material gas supplied to the reformer flows, and a raw material channel.
  • a pressure regulator that lowers the pressure, a booster that is provided in the raw material flow path and that increases the pressure of the raw material gas that has passed through the pressure regulator, and a raw material gas that is provided in the raw material flow path and that has passed through the pressure regulator.
  • a hydrodesulfurizer that removes sulfur compounds and a recycle channel that supplies the hydrogen-containing gas generated in the reformer to the raw material channel downstream of the pressure regulator and upstream of the hydrodesulfurizer and booster And comprising.
  • FIG. 1 is a block diagram illustrating an example of a schematic configuration of a hydrogen generator according to the first embodiment.
  • the hydrogen generator 100 of the present embodiment includes a raw material flow path 1, a pressure regulator 2 (Pressure controller), a booster 3, a hydrodesulfurizer 4, and a reformer 5. And a recycling flow path 6.
  • the reformer 5 generates a hydrogen-containing gas from the raw material gas by a reforming reaction.
  • the reforming reaction may be any reforming reaction, and specifically, steam reforming reaction (steam reforming), autothermal reaction (autothermalreforming) and partial oxidation reaction (partial oxidation reforming) are exemplified. More specifically, for example, the reformer 5 includes a reforming catalyst such as a Ru catalyst or a Ni catalyst therein, and uses a raw material gas and steam supplied from a water evaporator (not shown) to reform the steam. A hydrogen-containing gas is produced by the quality reaction.
  • the source gas contains at least an organic compound having carbon and hydrogen as constituent elements, and specific examples thereof include hydrocarbons such as natural gas, city gas, LPG, and LNG.
  • City gas refers to gas supplied from a gas company to households through piping.
  • Examples of the raw material supply source include an infrastructure of these gases and a cylinder for storing these gases.
  • a CO reducer for reducing carbon monoxide in the hydrogen-containing gas produced by the reformer 1 may be provided downstream of the reformer 1.
  • the CO reducer includes a shift converter having a shift catalyst that reduces carbon monoxide by a shift reaction, and CO removal that reduces carbon monoxide by at least one of an oxidation reaction and a methanation reaction. At least one of a CO remover including a catalyst is provided.
  • the raw material flow path 1 is a flow path through which the raw material gas supplied to the reformer 5 flows.
  • the raw material flow path 1 is a flow path from the supply source of the raw material gas to the reformer 5.
  • the pressure regulator 2 (step-down device) is provided in the raw material flow path 1 and has a function of reducing the pressure of the raw material gas.
  • a governor that mechanically reduces the pressure of the raw material gas
  • a proportional valve that electrically adjusts the pressure of the raw material gas, and the like are used.
  • the pressure regulator 2 may have any configuration as long as the pressure of the upstream source gas can be lower than the pressure of the downstream source gas.
  • the pressure dropped by the pressure regulator 2 may be increased as the pressure of the source gas is relatively increased.
  • the pressure of the source gas is relatively small (for example, 1 kPa in gauge pressure)
  • the pressure of the source gas is not lowered by the pressure regulator.
  • the pressure regulator 2 is configured so that the pressure in the raw material flow path 1 connected to the downstream end of the recycle flow path is equal to the recycle flow path 6 at the upper limit of the fluctuation range of the supply pressure of the raw material gas.
  • the pressure may be reduced to the pressure supplied to the raw material flow path 1 through.
  • a set value of the amount of hydrogen necessary for hydrodesulfurization for example, 1% or more is set as the volume ratio of hydrogen supplied to the raw material gas.
  • the pressure regulator 2 may reduce the pressure of the raw material gas and lower the fluctuation range of the pressure of the raw material gas downstream thereof than the fluctuation range of the pressure of the raw material gas upstream thereof.
  • it may be a pressure regulator that reduces the pressure of the raw material gas and adjusts it to a predetermined pressure range.
  • the pressure regulator include a governor and a regulator.
  • the supply pressure of the infrastructure is generally in the range of 1.0 kPa to 2.5 kPa according to JIS standards. It has been. However, by using the pressure regulator, even when such a change occurs, the pressure of the raw material gas immediately below the pressure regulator is adjusted to a range of 0.8 kPa to 1.0 kPa, for example.
  • the supply pressure of the LPG cylinder is generally in the range of 2.0 kPa to 3.3 kPa according to JIS standards. It has been.
  • the pressure regulator may be configured such that the pressure of the raw material gas immediately below it is adjusted to the same value as when the raw material gas is city gas, for example, 0.8 kPa to 1.0 kPa. Thereby, the design is made common to different types of source gases.
  • you may comprise so that the pressure of the raw material gas just under the pressure regulator 2 may become a different range between city gas and LPG gas.
  • the booster 3 is provided in the raw material flow path 1 and increases the pressure of the raw material gas that has passed through the pressure regulator 2.
  • a booster pump or the like is exemplified.
  • the booster may be any device as long as the pressure of the source gas downstream can be higher than the pressure of the source gas upstream.
  • the hydrodesulfurizer 4 is provided in the raw material flow path 1 and removes sulfur compounds in the raw material gas that has passed through the pressure regulator 2.
  • the hydrodesulfurizer 4 includes a hydrodesulfurization agent.
  • this hydrodesulfurization agent includes, for example, a CoMo catalyst that converts a sulfur compound in a raw material gas into hydrogen sulfide, and a ZnO catalyst and a CuZn catalyst that are adsorbents that adsorb the converted hydrogen sulfide.
  • At least one of them may be used, and as a catalyst species having both a function of converting a sulfur compound into hydrogen sulfide and a function of adsorbing hydrogen sulfide, Cu—Zn—Ni-based and Cu—Zn— It is good also as a form provided with at least any one of Fe-type catalyst.
  • the sulfur compound may be artificially added to the raw material as an odorous component, or may be a natural sulfur compound derived from the raw material itself.
  • TBM tertiary-butylmercaptan
  • DMS dimethyl sulfide
  • THT tetrahydrothiophene
  • COS carbonyl sulfide
  • hydrogen sulfide hydrogen sulfide (hydrogen sulfide), etc.
  • the booster 3 is disposed upstream of the hydrodesulfurizer 4.
  • the booster 3 and the hydrodesulfurizer 4 is disposed upstream. is there.
  • the recycle channel 6 is a channel for supplying the hydrogen-containing gas generated in the reformer 5 to the raw material channel 1 downstream of the pressure regulator 2 and upstream of the hydrodesulfurizer 4 and the booster 3. is there.
  • the gas flowing through the recycle channel 6 is referred to as recycle gas.
  • the recycle channel 6 branches from the channel through which the hydrogen-containing gas that has passed through the reformer 5 flows, and is connected to the raw material channel 1 from the pressure regulator 2 to the booster 3. .
  • the upstream end of the recycle channel 6 may be connected to any location as long as the hydrogen-containing gas that has passed through the reformer 5 flows.
  • the upstream end may be connected to a flow path from the reformer 1 to the CO reducer, or connected to the CO reducer. Or may be connected to a flow path downstream of the CO reducer.
  • the CO reducer includes a transformer that reduces carbon monoxide by a shift reaction and a CO remover that reduces carbon monoxide by at least one of an oxidation reaction and a methanation reaction
  • the recycle flow path 6 You may comprise so that the upstream end of may be connected to the flow path between a transformer and a CO remover.
  • the hydrogen-using device is a device that uses the hydrogen-containing gas supplied from the hydrogen generation apparatus 100, and examples thereof include a fuel cell and a hydrogen storage container.
  • downstream end of the recycle channel 6 can be used as a raw material as long as hydrogen-containing gas can be supplied to the raw material channel 1 downstream from the pressure regulator 2 and upstream from the hydrodesulfurizer 4 and the booster 3. You may provide in any location of the flow path 1.
  • the downstream end of the recycle flow path 6 is connected to the raw material flow path 1 from the pressure regulator 2 to the booster 3.
  • the downstream end of the recycle channel 6 is connected to the raw material channel 1 from the pressure regulator 2 to the hydrodesulfurizer 4. Is done.
  • the downstream end of the recycle channel 6 is connected to the raw material channel 1 downstream from the pressure regulator 2 and upstream from the hydrodesulfurizer 4 and the booster 3. Therefore, even if the supply pressure of the raw material gas is high, the pressure is reduced downstream of the pressure regulator 2, so that a decrease in the differential pressure between the upstream end and the downstream end of the recycle channel is suppressed. Therefore, even if the supply pressure of the raw material gas is high, a decrease in the flow rate of the recycle gas is suppressed as compared with the conventional hydrogen generator.
  • the output of the booster 3 is increased to reduce the pressure at the upstream end of the recycling flow path in order to suppress a decrease in the differential pressure between the upstream end and the downstream end of the recycling flow path.
  • the reformer 5 generates more hydrogen-containing gas than necessary.
  • a decrease in the differential pressure may be suppressed without increasing the output of the booster 3 and generating more hydrogen gas than necessary.
  • the pressure regulator 2 is the above-described pressure regulator, fluctuations in the differential pressure between the upstream end and the downstream end of the recycling flow path are suppressed as compared with the case where no pressure regulator is provided. The possibility of being deficient or excessive is reduced.
  • the pressure regulator 2 is not provided, and the gas pressure directly below the booster 3 is constant, the differential pressure between the upstream end and the downstream end of the recycle channel is 1 It will fluctuate with a width of .5 kPa.
  • the flow rate of the recycled gas also varies.
  • the flow rate of the recycle gas is insufficient with respect to the flow rate required for hydrodesulfurization, desulfurization in the hydrodesulfurizer 4 becomes insufficient, and the reforming catalyst of the reformer 5 may be poisoned. There is sex.
  • the flow rate of the recycle gas becomes excessive with respect to the amount required for hydrodesulfurization, the water vapor contained in the recycle gas is excessive, and the hydrodesulfurization agent of the hydrodesulfurizer 4 is deteriorated. There is sex.
  • the pressure regulator when the gas pressure immediately below the booster 3 is constant, the fluctuation range of the differential pressure between the upstream end and the downstream end of the recycle flow path is reduced to, for example, 0.2 kPa. The possibility that the above problem will occur is reduced.
  • the hydrogen generator according to the second embodiment is provided with a raw material in the raw material channel upstream of the junction of the raw material channel and the recycle channel.
  • a room temperature desulfurizer for removing sulfur compounds therein at room temperature is provided, and the pressure regulator is disposed in the raw material flow path upstream of the room temperature desulfurizer.
  • FIG. 2 is a block diagram showing an example of a schematic configuration of the hydrogen generator according to the second embodiment.
  • the hydrogen generator 200 of this embodiment includes a room temperature desulfurizer 7.
  • the room temperature desulfurizer 7 includes an adsorbent that adsorbs sulfur compounds at room temperature.
  • adsorbent for example, activated carbon, silver zeolite (Ag-zeolite), or the like can be used.
  • the term “normal temperature” is used because it is relatively close to the normal temperature range compared to the operating temperature of the hydrodesulfurizer 4 (for example, around 300 ° C.), and the used desulfurizing agent is used as the desulfurizing agent from the normal temperature range. It is meant to include temperatures that function effectively.
  • the raw material flow path 1 branches into two downstream of the pressure regulator 2, the second on-off valve 22 and the room temperature desulfurizer 7 are provided on one side, and the first on-off valve 21 is provided on the other side. It is done.
  • the branched raw material flow path 1 merges downstream of the room temperature desulfurizer 7 and is connected to the booster 3 downstream of the merge portion.
  • the room temperature desulfurizer 7 is provided in the raw material flow path 1 downstream of the pressure regulator 2 and upstream of the junction of the raw material flow path 1 and the recycle flow path 6.
  • the upstream here refers to at least the normal temperature It means that the portion where the raw material flow path 1 where the desulfurizer 7 is provided branches is upstream of the junction of the raw material flow path 1 and the recycle flow path 6.
  • the first on-off valve 21 and the second on-off valve 22 function as a switch for switching to which side of the branched material flow path 1 the material that has passed through the pressure regulator 2 flows.
  • other switching devices such as a three-way valve may be used.
  • the second on-off valve 22 is disposed upstream of the room temperature desulfurizer 7, but the second on-off valve 22 may be disposed downstream of the room temperature desulfurizer 7.
  • the recycle channel 6 is provided with a third on-off valve 23.
  • the first on-off valve 21, the second on-off valve 22, and the third on-off valve 23, for example, electromagnetic valves can be used.
  • the configuration other than the above can be configured in the same manner as that of any one of the first embodiment and its modifications.
  • 1 and 2 are denoted by the same reference numerals and names, and detailed description thereof is omitted.
  • the sulfur compound in the raw material is removed by the room temperature desulfurizer 7. Specifically, the first on-off valve 21 is closed and the second on-off valve 22 is opened so that the raw material gas that has passed through the pressure regulator 2 passes through the room temperature desulfurizer 7. Further, the third on-off valve 23 is closed.
  • the raw material gas is supplied to the reformer 5 in order to compensate for a decrease in internal pressure or gas contraction of the reformer 5 due to a temperature decrease of the reformer 5.
  • the operation of replenishing is executed.
  • desulfurization is performed using the room temperature desulfurizer 7.
  • the internal pressure drop of the reformer 5 occurs in the hydrogen generator 100 configured so that the gas flow path downstream of the reformer 5 is closed by the valve when the operation is stopped, and the reformer 5 is sealed.
  • the gas shrinkage of the reformer 5 occurs in the hydrogen generator 100 configured so that the gas flow path downstream of the reformer 5 is not closed so that the reformer 5 is opened to the atmosphere even after the operation is stopped.
  • the above operations can be executed by a controller (not shown).
  • the configuration of the controller can be the same as in the fourth embodiment.
  • the hydrogen generator of the third embodiment is the same as that of the hydrogen generator according to at least one of the first embodiment, the second embodiment, and the modifications thereof.
  • FIG. 3 is a block diagram showing an example of a schematic configuration of the hydrogen generator according to the second embodiment.
  • the hydrogen generator 300 of this embodiment includes a pressure detector 8.
  • the pressure detector 8 detects the pressure in the raw material flow path 1. Specifically, for example, the pressure of the raw material gas in the raw material flow path 1 is detected by using a diaphragm type pressure sensor (diaphragm pressure censor), a bellows type pressure sensor (bellows pressure censor), or the like.
  • a diaphragm type pressure sensor diaphragm pressure censor
  • a bellows type pressure sensor bellows pressure sensor
  • the configuration other than the above can be configured in the same manner as any one of the first embodiment, the second embodiment, and their modifications. Therefore, components common to FIGS. 1 and 3 are given the same reference numerals and names, and detailed description thereof is omitted.
  • the pressure detector 8 detects the gas supply pressure of the source gas supply source located upstream of the source channel 1. If the supply pressure drops abnormally for some reason due to the supply of the raw material gas, if this is left unattended, there is a possibility that the hydrogen generator 300 will be broken or abnormal.
  • the specific processing method in the case where the pressure detector 8 detects an abnormal decrease in the raw material is not particularly limited.
  • the operation of the hydrogen generator 300 may be stopped, the operation of the booster 3 may be stopped, or the raw material gas is changed by closing a not-illustrated on-off valve provided in the raw material flow path 1. Suction by the booster 3 may be prevented.
  • the hydrogen generator according to the fourth embodiment includes an on-off valve provided in the raw material flow path and a hydrogen generator in the hydrogen generator according to at least one of the first to third embodiments and their modifications. After stopping the hydrogen generation operation, the open / close valve is opened and the reformer is operated in response to a decrease in internal pressure of the reformer due to a decrease in the temperature of the reformer or a gas contraction in the reformer. And a controller for supplying the raw material gas.
  • FIG. 4 is a block diagram illustrating an example of a schematic configuration of the hydrogen generator according to the fourth embodiment.
  • the hydrogen generator 400 of this embodiment includes the on-off valve 9, the pressure detector 13, and the controller 10.
  • the on-off valve 9 can be a solenoid valve, for example.
  • the on-off valve 9 is communicably connected to the controller 10 and is opened and closed based on the control of the controller 10.
  • the on-off valve 9 is disposed in the raw material flow path 1 downstream of the booster 3 and upstream of the hydrodesulfurizer 4, but is not limited to this configuration. Can be disposed at any location as long as it is a raw material flow path 1.
  • the pressure detector 13 detects the internal pressure of the reformer 5.
  • the controller 10 After stopping the hydrogen generation operation in the hydrogen generator 400, the controller 10 opens the on-off valve 9 and operates the booster 3 in response to a decrease in internal pressure due to a decrease in the temperature of the reformer 5.
  • the raw material is supplied to the vessel 5 (hereinafter referred to as “compensation operation”).
  • the controller 10 only needs to have a control function, and includes an arithmetic processing unit (not shown) and a storage unit (not shown) for storing a control program.
  • Examples of the arithmetic processing unit include an MPU and a CPU.
  • a memory is exemplified as the storage unit.
  • the controller may be composed of a single controller that performs centralized control, or may be composed of a plurality of controllers that perform distributed control in cooperation with each other.
  • the supplementary pressure operation refers to, for example, supplying gas to the interior of the reformer so as to compensate for at least part of the pressure drop caused by the lowering of the internal temperature of the reformer after the hydrogen generator is stopped. Say to do. An amount of gas exceeding the supply pressure of the raw material upstream of the pressure regulator 2 may be supplied. More specifically, for example, if the supply pressure of the raw material upstream of the pressure regulator 2 is P1, the booster 3 is operated during the pressure compensation operation, and the internal pressure of the reformer 5 is set to P2 or more which is larger than P1. Thus, the raw material gas is supplied into the reformer 5.
  • a pressure detector for detecting the pressure inside the reformer 5 may be used, but the pressure inside the reformer 5 is indirectly detected.
  • a detector may be used. Examples of the detector that indirectly detects the pressure inside the reformer 5 include a temperature detector that detects the temperature of the reformer, and a timer that measures the elapsed time since the reformer 5 was sealed. Etc.
  • a correlation between the temperature of the reformer 5 after sealing the reformer 5 and a decrease in internal pressure is obtained in advance through experiments or the like, and a temperature condition that requires a pressure compensation operation from this correlation Is stored in the storage unit. Then, when the detected temperature detected by the temperature detector satisfies the temperature condition stored in the storage unit, the pressure compensation operation may be executed under the control of the controller 10.
  • a timer when a timer is used, a correlation between an elapsed time after sealing the reformer 5 and a decrease in the internal pressure of the reformer 5 is obtained in advance by experiments or the like, and a time condition that requires a pressure compensation operation from this correlation Is stored in the storage unit. Then, if the elapsed time detected by the timer satisfies the time condition stored in the storage unit, the pressure compensation operation may be executed under the control of the controller 10.
  • the configuration other than the above can be configured similarly to any one of the first to third embodiments and their modifications. Therefore, components common to FIGS. 1 and 4 are given the same reference numerals and names, and detailed description thereof is omitted.
  • FIG. 5 is a flowchart illustrating an example of an operation method of the hydrogen generator according to the fourth embodiment. The operation shown in FIG. 5 is executed by the controller 10 controlling each part of the hydrogen generator 400.
  • the booster 3 When the hydrogen generation operation is stopped (start), the booster 3 is stopped. Moreover, the on-off valve 9 (not shown) provided in the flow path downstream of the on-off valve 9 and the reformer 5 is also closed, and the reformer 5 is sealed.
  • the pressure detector detects the internal pressure of the reformer 5 (step S101). When the detected pressure becomes equal to or lower than the first pressure threshold value P1 (Yes in step S102), the on-off valve 9 is opened and the booster 3 is operated (step S103), and the state is maintained for a predetermined time T1. (Step S104). As a result, the raw material gas is supplied into the reformer 5 so as to compensate for the lowering of the internal pressure of the reformer 5. Thereafter, the on-off valve 9 is closed, the operation of the booster 3 is stopped (step S104), and the pressure compensation operation ends (end).
  • the compensation operation may be performed in a plurality of times.
  • the predetermined time T1 is set so that an amount of raw material gas necessary to compensate for the decrease in internal pressure of the reformer 5 is supplied to the reformer 5.
  • the stoppage of the supplementary pressure operation may be determined by the detected pressure of the pressure detector 13 instead of the execution time of the supplementary pressure operation. Specifically, the supplementary pressure operation is continued and stopped until the detected pressure of the pressure detector 13 becomes equal to or higher than the second pressure threshold value P2.
  • the hydrogen generator of this modification is the same as that of the first to third embodiments and the hydrogen generator according to at least one of those modifications, in the on-off valve provided in the raw material flow path, Control of opening the on-off valve and operating the booster to supply the raw material gas to the reformer against the gas contraction in the reformer due to the temperature drop of the reformer after the hydrogen generation operation is stopped With a vessel.
  • This modification is configured such that the reformer 5 is opened to the atmosphere after the hydrogen generation operation of the hydrogen generator 400 is stopped. Specifically, no on-off valve is provided in the path downstream of the reformer 5.
  • the oxidation deterioration of the catalyst means at least one of oxidation deterioration of the reforming catalyst, oxidation deterioration of the shift catalyst, and oxidation deterioration of the CO removal catalyst.
  • a method of opening the on-off valve 9 and supplying the raw material gas to the reformer 5 to suppress the inflow of outside air from the flow path downstream of the reformer 5 can be considered. Since the apparatus is provided with the pressure regulator 2, the gas pressure downstream of the pressure regulator 2 is lower than upstream. Therefore, even if the on-off valve 9 is opened, the raw material gas is not replenished to the flow path downstream of the reformer 5, and the catalyst may be oxidized and deteriorated by the outside air. Therefore, the controller 10 opens the on-off valve 9 and operates the booster 3 to compensate for gas contraction in the reformer 5. Thereby, the raw material gas is supplied to the gas flow path downstream of the reformer 5, and the possibility that the catalyst is oxidized and deteriorated is reduced.
  • FIG. 6 is a block diagram showing an example of a schematic configuration of a fuel cell system according to a modification of the fourth embodiment.
  • the fuel cell system of this modification includes a temperature detector 14.
  • the temperature detector 14 detects the temperature of the reformer 5.
  • the detector for detecting the temperature of the reformer 5 may be a temperature detector for directly detecting the temperature of the reformer 5 or a detector for detecting it indirectly.
  • Examples of the detector that indirectly detects the temperature of the reformer 5 include a timer that measures an elapsed time after the hydrogen generation operation of the hydrogen generator 400 is stopped.
  • the controller 10 After stopping the hydrogen generation operation in the hydrogen generator, the controller 10 opens the on-off valve and operates the booster against the gas contraction in the reformer accompanying the temperature drop of the reformer, Supply raw material gas to the reformer (hereinafter referred to as replenishment operation).
  • the timing of the replenishment operation is determined based on the temperature detected by the temperature detector 14 that detects the temperature of the reformer 5.
  • the temperature detector 14 when the temperature detector 14 is used as a detector for detecting the temperature of the reformer 5, the temperature of the reformer 5 after the hydrogen generation operation of the hydrogen generator 400 is stopped and the flow path downstream of the reformer 5. A correlation with the inflow amount of outside air from is obtained in advance through experiments or the like, and a temperature condition that requires a replenishment operation is stored in the storage unit from this correlation. Then, when the detected temperature detected by the temperature detector satisfies the temperature condition stored in the storage unit, the pressure compensation operation may be executed under the control of the controller 10.
  • the elapsed time after the hydrogen generation operation of the hydrogen generator is stopped and the inflow amount of outside air from the flow path downstream of the reformer 5.
  • a time condition that requires a replenishment operation is stored in the storage unit from this correlation. Then, when the elapsed time detected by the timer satisfies the time condition stored in the storage unit, the replenishment operation may be executed under the control of the controller 10.
  • step S102 is a step of determining whether or not the temperature detected by the temperature detector 14 is equal to or higher than a predetermined threshold T1. Since this is the same, the description thereof is omitted.
  • a fuel cell system generates power using a hydrogen generator according to at least one of the first to fourth embodiments and their modifications, and a hydrogen-containing gas supplied from the hydrogen generator. And a fuel cell.
  • FIG. 7 is a block diagram showing an example of a schematic configuration of a fuel cell system according to the fifth embodiment.
  • the fuel cell system 500 of this embodiment includes a hydrogen generator 100 and the fuel cell 20.
  • the fuel cell 20 is a fuel cell that generates electricity using a hydrogen-containing gas supplied from a hydrogen generator.
  • the fuel cell may be any type of fuel cell, such as a polymer electrolyte fuel cell (PEFC), a solid oxide fuel cell (SOFC), a phosphoric acid fuel cell (PAFC), etc. Can be used.
  • PEFC polymer electrolyte fuel cell
  • SOFC solid oxide fuel cell
  • PAFC phosphoric acid fuel cell
  • the reformer and the fuel cell stack are separately configured in the fuel cell unit.
  • an indirect internal reforming type having a reforming section and a fuel cell section that perform reforming reactions individually, and an internal reforming type that also performs a reforming reaction inside the fuel cell body Any of these may be used. That is, a form in which a reformer is built in the fuel cell may be employed, and the fuel cell of the present invention includes such a form.
  • the hydrogen generator 100 may be configured in the same manner as any one of the first to fourth embodiments and their modifications. Constituent elements common to FIG. 1 and FIG. 7 are given the same reference numerals and names, and detailed descriptions thereof are omitted.
  • FIG. 8 is a block diagram illustrating an example of a schematic configuration of a fuel cell system according to a modification of the fifth embodiment.
  • a solid oxide fuel cell SOFC
  • the fuel cell system 500 ⁇ / b> A of the present modification includes a hydrogen generator 100, an evaporator 11, an air supplier 12, and a fuel cell main body 30.
  • the evaporator 11 evaporates the water supplied from the water supply source, and supplies the obtained water vapor to the reformer 5.
  • the air supplier 12 supplies air as an oxidant gas to the fuel cell main body 30.
  • the fuel cell main body 30 is a fuel cell stack, and generates electricity using hydrogen supplied from the reformer 5 and air supplied from the air supplier 12.
  • the reformer 5, the evaporator 11, and the fuel cell body 30 constitute a hot module 40.
  • the entire hot module 40 is heated as a whole.
  • the hydrogen generator 100 may be configured in the same manner as any one of the first to fourth embodiments and their modifications. Constituent elements common to FIG. 1 and FIG. 8 are denoted by the same reference numerals and names, and detailed description thereof is omitted.
  • the recycle flow path 6 is branched from the flow path connecting the reformer 5 and the fuel cell main body 30.
  • the recycle flow path 6 is not necessarily limited to such a configuration. Gas may be removed.
  • the gas inlet of the recycle flow path 6 is connected to the flow path through which off-fuel gas discharged from the fuel cell main body 30 flows, and the off-fuel gas is recycled gas from the pressure regulator 2 to the booster 3. May be supplied.
  • the hydrogen generator and fuel cell system of the present invention are capable of suppressing a decrease in the flow rate of the hydrogen gas flowing through the recycle flow path as compared with the conventional hydrogen generator even when the supply pressure of the raw material gas is high. It is useful as a battery system.

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Abstract

A hydrogen generation device (100) comprising: a reformer (5) for generating hydrogen-containing gas from crude gas; a crude material flow path (1) through which crude gas supplied to the reformer flows; a pressure regulator (2) for lowering the pressure of the crude gas, the pressure regulator being provided to the crude material flow path; a pressure booster (3) for boosting the pressure of the crude gas having passed through the pressure regulator, the pressure booster being provided to the crude material flow path; a hydrodesulfurizer (4) for removing sulfur compounds in the crude gas having passed through the pressure regulator, the hydrodesulfurizer being provided to the crude material flow path; and a recycle flow path (6) for supplying hydrogen-containing gas generated by the reformer to the crude material flow path downstream of the pressure regulator and upstream of the hydrodesulfurizer and the pressure booster.

Description

水素生成装置及び燃料電池システムHydrogen generator and fuel cell system

 本発明は、水素生成装置、燃料電池システム、及びその運転方法に関する。より詳しくは、原料ガス中の硫黄化合物を除去する水添脱硫器を備えた水素生成装置、及び燃料電池システムに関する。 The present invention relates to a hydrogen generator, a fuel cell system, and an operation method thereof. More specifically, the present invention relates to a hydrogen generator equipped with a hydrodesulfurizer that removes sulfur compounds in a raw material gas, and a fuel cell system.

 小型装置でも高効率な発電を可能とする燃料電池は、分散型エネルギー供給源の発電システムとして開発が進められている。発電時の燃料となる水素ガスは、その供給源が、一般的なインフラストラクチャとして整備されていない。そこで例えば都市ガス、プロパンガス等の既存のインフラストラクチャから供給される原料ガスを利用し、それらの原料ガスと水との改質反応により水素含有ガスを生成させる水素生成装置が併設される。 Development of fuel cells that enable high-efficiency power generation even with small devices is being developed as a power generation system for distributed energy sources. The supply source of hydrogen gas as fuel for power generation is not maintained as a general infrastructure. Therefore, for example, a hydrogen generator that uses a source gas supplied from an existing infrastructure such as city gas or propane gas and generates a hydrogen-containing gas by a reforming reaction between the source gas and water is additionally provided.

 水素生成装置は、原料ガスと水とを改質反応させる改質器、一酸化炭素と水蒸気を水性ガスシフト反応(water-gas-shift reaction)させる変成器、及び、一酸化炭素を主に空気等の酸化ガスで酸化させるCO除去器を設ける構成がとられることが多い。これらの反応器には、各反応に適した触媒、例えば、改質器にはRu触媒やNi触媒等、変成器にはCu-Zn触媒等、CO除去器にはRu触媒等が用いられている。 The hydrogen generator is a reformer that reforms the raw material gas and water, a gas-shift-reaction converter that converts carbon monoxide and water vapor, and carbon monoxide, mainly air. In many cases, a configuration is provided in which a CO remover that is oxidized with an oxidizing gas is provided. In these reactors, a catalyst suitable for each reaction is used. For example, a Ru catalyst or Ni catalyst is used for the reformer, a Cu—Zn catalyst is used for the shifter, and a Ru catalyst is used for the CO remover. Yes.

 それぞれの反応器には適した温度がある。具体的には、改質器は600~700℃程度、変成器は350~200℃程度、CO除去器は200℃~100℃程度で使用されることが多い。特に固体高分子型燃料電池では、一酸化炭素による電極被毒が起こりやすい。このため、供給される水素含有ガス中の一酸化炭素濃度は数十体積ppm以下に抑える必要がある。CO除去器では一酸化炭素を酸化させることによって一酸化炭素濃度を低減する。 Each reactor has a suitable temperature. Specifically, the reformer is often used at about 600 to 700 ° C., the transformer is used at about 350 to 200 ° C., and the CO remover is used at about 200 to 100 ° C. in many cases. In particular, in polymer electrolyte fuel cells, electrode poisoning due to carbon monoxide tends to occur. For this reason, it is necessary to suppress the carbon monoxide concentration in the supplied hydrogen-containing gas to several tens of ppm by volume or less. The CO remover reduces the carbon monoxide concentration by oxidizing carbon monoxide.

 一方、都市ガス等の原料ガスには硫黄化合物が含まれている。硫黄化合物は、特に改質触媒の被毒物質であるので、何らかの方法で除去する必要がある。常温吸着により除去する方法(例えば、特許文献1参照)や水素を用いて水添脱硫により除去する方法(例えば、特許文献2参照)を採用した水素生成装置が提案されている。常温吸着脱硫は加熱と水素を必要としないため取扱が簡便である反面、脱硫容量が大きくない。水添脱硫は加熱と水素を必要とし取扱が簡便ではないが、脱硫容量が大きいといった特徴がある。ここで、起動時に常温吸着脱硫を用い、水素が発生できるようになってから水添脱硫に切り換える水素生成装置も提案されている(例えば、特許文献2、3参照)。 On the other hand, source gases such as city gas contain sulfur compounds. Since the sulfur compound is a poisoning substance for the reforming catalyst, it must be removed by some method. Hydrogen generators have been proposed that employ a method of removing by room temperature adsorption (see, for example, Patent Document 1) or a method of removing by hydrodesulfurization using hydrogen (see, for example, Patent Document 2). Room temperature adsorptive desulfurization is easy to handle because it does not require heating and hydrogen, but the desulfurization capacity is not large. Hydrodesulfurization requires heating and hydrogen and is not easy to handle, but has a feature of large desulfurization capacity. Here, a hydrogen generation apparatus that uses room temperature adsorptive desulfurization at start-up and switches to hydrodesulfurization after hydrogen can be generated has also been proposed (see, for example, Patent Documents 2 and 3).

 また、常温吸着脱硫と水添脱硫とを併用する水素生成装置も提案されている(例えば、特許文献4参照)。 Also, a hydrogen generator that uses both room temperature adsorption desulfurization and hydrodesulfurization has been proposed (see, for example, Patent Document 4).

 水添脱硫器を用いる水素生成装置は、改質器を通過した水素含有ガスが流れる流路から分岐したリサイクル流路を介して、水添脱硫器に供給される原料に水素含有ガスが供給されるよう構成されている。 In a hydrogen generator using a hydrodesulfurizer, a hydrogen-containing gas is supplied to a raw material supplied to the hydrodesulfurizer via a recycle channel branched from a channel through which the hydrogen-containing gas that has passed through the reformer flows. It is comprised so that.

特開2004-228016号公報JP 2004-228016 A 特開平1-275697号公報Japanese Patent Laid-Open No. 1-275697 特許第4264791号公報Japanese Patent No. 4264791 特開平8-293315号公報JP-A-8-293315

 上記のように、水添脱硫を用いている水素生成装置では、原料ガスの供給圧が高くなると、リサイクル流路を流れる水素含有ガスの量が低下し、水添脱硫器に水添脱硫に必要な量の水素が供給されない可能性がある。 As described above, in a hydrogen generator using hydrodesulfurization, when the supply pressure of the raw material gas increases, the amount of hydrogen-containing gas flowing through the recycle flow path decreases, and the hydrodesulfurizer requires hydrodesulfurization. There is a possibility that an excessive amount of hydrogen is not supplied.

 本発明は、上記課題を解決するものであり、原料ガスの供給圧が高くても、従来の水素生成装置に比べ、リサイクル流路を流れる水素ガス流量の低下が抑制される水素生成装置、燃料電池、及びその運転方法を提供することを目的とする。 The present invention solves the above-mentioned problem, and even when the supply pressure of the raw material gas is high, a hydrogen generator and fuel in which a decrease in the flow rate of hydrogen gas flowing through the recycle channel is suppressed as compared with a conventional hydrogen generator It is an object to provide a battery and a method for operating the battery.

 本発明者らは、水添脱硫を採用している水素生成装置において、鋭意検討を行った。その結果、以下の知見を得た。 The present inventors have intensively studied in a hydrogen generator that employs hydrodesulfurization. As a result, the following knowledge was obtained.

 原料ガスの供給圧が高くなると、リサイクル流路の下流端の圧力が高くなるので、リサイクルガス流路の上流端と下流端との差圧が低下し、水素含有ガスの流量が低下する。 When the supply pressure of the raw material gas increases, the pressure at the downstream end of the recycle channel increases, so the differential pressure between the upstream end and the downstream end of the recycle gas channel decreases, and the flow rate of the hydrogen-containing gas decreases.

 そこで、原料ガスの供給源と改質器とを接続する原料流路において、圧力調整器と昇圧器とを、原料ガスの流れの向きに対してこの順に配設し、かつリサイクル流路の下流端を圧力調整器から昇圧器までの原料流路に接続する。すると、原料ガスの供給圧が高くても圧力調整器で圧力が低下するため、リサイクル流路の上流端と下流端との間の差圧の低下が抑制される。 Therefore, in the raw material flow path connecting the raw material gas supply source and the reformer, the pressure regulator and the booster are arranged in this order with respect to the flow direction of the raw material gas, and downstream of the recycling flow path. Connect the end to the raw material flow path from the pressure regulator to the booster. Then, even if the supply pressure of the raw material gas is high, the pressure is reduced by the pressure regulator, so that a reduction in the differential pressure between the upstream end and the downstream end of the recycle channel is suppressed.

 すなわち上記課題を解決するために、本発明の水素生成装置は、原料ガスから水素含有ガスを生成する改質器と、前記改質器に供給される原料ガスが流れる原料流路と、前記原料流路に設けられ、原料ガスの圧力を降下させる圧力調整器と、前記原料流路に設けられ、前記圧力調整器を通過した原料ガスの圧力を上昇させる昇圧器と、前記原料流路に設けられ、前記圧力調整器を通過した原料ガス中の硫黄化合物を除去する水添脱硫器と、前記改質器で生成された水素含有ガスを前記圧力調整器よりも下流かつ前記水添脱硫器及び前記昇圧器よりも上流の前記原料流路へと供給するリサイクル流路と、を備える。 That is, in order to solve the above problems, the hydrogen generator of the present invention includes a reformer that generates a hydrogen-containing gas from a raw material gas, a raw material channel through which the raw material gas supplied to the reformer flows, and the raw material A pressure regulator provided in the flow path for reducing the pressure of the raw material gas; a booster provided in the raw material flow path for raising the pressure of the raw material gas that has passed through the pressure regulator; and provided in the raw material flow path. A hydrodesulfurizer that removes sulfur compounds in the raw material gas that has passed through the pressure regulator, and a hydrogen-containing gas generated in the reformer downstream of the pressure regulator and the hydrodesulfurizer, and And a recycle flow path for supplying the raw material flow path upstream of the booster.

 また、本発明の燃料電池システムは、上記水素生成装置と、前記水素生成装置から供給される水素含有ガスを用いて発電する燃料電池とを備える。 The fuel cell system of the present invention includes the hydrogen generator and a fuel cell that generates power using a hydrogen-containing gas supplied from the hydrogen generator.

 本発明の水素生成装置、及び燃料電池システムによれば、原料ガスの供給圧が高くても、従来の水素生成装置に比べ、リサイクル流路を流れる水素ガス流量の低下が抑制される。 According to the hydrogen generation device and the fuel cell system of the present invention, even if the supply pressure of the raw material gas is high, a decrease in the flow rate of the hydrogen gas flowing through the recycle channel is suppressed as compared with the conventional hydrogen generation device.

図1は、第1実施形態にかかる水素生成装置の概略構成の一例を示すブロック図である。FIG. 1 is a block diagram illustrating an example of a schematic configuration of a hydrogen generator according to the first embodiment. 図2は、第2実施形態にかかる水素生成装置の概略構成の一例を示すブロック図である。FIG. 2 is a block diagram illustrating an example of a schematic configuration of the hydrogen generator according to the second embodiment. 図3は、第3実施形態にかかる水素生成装置の概略構成の一例を示すブロック図である。FIG. 3 is a block diagram illustrating an example of a schematic configuration of the hydrogen generator according to the third embodiment. 図4は、第4実施形態にかかる水素生成装置の概略構成の一例を示すブロック図である。FIG. 4 is a block diagram illustrating an example of a schematic configuration of the hydrogen generator according to the fourth embodiment. 図5は、第4実施形態にかかる水素生成装置の動作方法の一例を示すフローチャートである。FIG. 5 is a flowchart illustrating an example of an operation method of the hydrogen generator according to the fourth embodiment. 図6は、第4実施形態の変形例にかかる燃料電池システムの概略構成の一例を示すブロック図である。FIG. 6 is a block diagram illustrating an example of a schematic configuration of a fuel cell system according to a modification of the fourth embodiment. 図7は、第5実施形態にかかる燃料電池システムの概略構成の一例を示すブロック図である。FIG. 7 is a block diagram illustrating an example of a schematic configuration of a fuel cell system according to the fifth embodiment. 図8は、第5実施形態の変形例にかかる燃料電池システムの概略構成の一例を示すブロック図である。FIG. 8 is a block diagram illustrating an example of a schematic configuration of a fuel cell system according to a modification of the fifth embodiment.

 (第1実施形態)
 第1実施形態の水素生成装置は、原料ガスから水素含有ガスを生成する改質器と、改質器に供給される原料ガスが流れる原料流路と、原料流路に設けられ、原料ガスの圧力を降下させる圧力調整器と、原料流路に設けられ、圧力調整器を通過した原料ガスの圧力を上昇させる昇圧器と、原料流路に設けられ、圧力調整器を通過した原料ガス中の硫黄化合物を除去する水添脱硫器と、改質器で生成された水素含有ガスを圧力調整器よりも下流かつ水添脱硫器及び昇圧器よりも上流の原料流路へと供給するリサイクル流路と、を備える。
(First embodiment)
The hydrogen generator of the first embodiment includes a reformer that generates a hydrogen-containing gas from a raw material gas, a raw material channel through which the raw material gas supplied to the reformer flows, and a raw material channel. A pressure regulator that lowers the pressure, a booster that is provided in the raw material flow path and that increases the pressure of the raw material gas that has passed through the pressure regulator, and a raw material gas that is provided in the raw material flow path and that has passed through the pressure regulator. A hydrodesulfurizer that removes sulfur compounds and a recycle channel that supplies the hydrogen-containing gas generated in the reformer to the raw material channel downstream of the pressure regulator and upstream of the hydrodesulfurizer and booster And comprising.

 かかる構成では、原料ガスの供給圧が高くても、従来の水素生成装置に比べ、リサイクル流路を流れる水素ガス流量の低下が抑制される。 In such a configuration, even if the supply pressure of the raw material gas is high, a decrease in the flow rate of the hydrogen gas flowing through the recycle channel is suppressed as compared with the conventional hydrogen generator.

 [装置構成]
 図1は、第1実施形態にかかる水素生成装置の概略構成の一例を示すブロック図である。
[Device configuration]
FIG. 1 is a block diagram illustrating an example of a schematic configuration of a hydrogen generator according to the first embodiment.

 図1に示す例では、本実施形態の水素生成装置100は、原料流路1と、圧力調整器2(Pressure controller)と、昇圧器3と、水添脱硫器4と、改質器5と、リサイクル流路6とを備える。 In the example shown in FIG. 1, the hydrogen generator 100 of the present embodiment includes a raw material flow path 1, a pressure regulator 2 (Pressure controller), a booster 3, a hydrodesulfurizer 4, and a reformer 5. And a recycling flow path 6.

 改質器5は、改質反応により、原料ガスから水素含有ガスを生成する。改質反応は、いずれの改質反応でもよく、具体的には、水蒸気改質反応(steam reforming)、オートサーマル反応(autothermalreforming)及び部分酸化反応(partial oxidation reforming)が例示される。より具体的には例えば、改質器5は、その内部にRu触媒やNi触媒等の改質触媒を備え、原料ガスと、図示されない水蒸発器から供給される水蒸気とを用いて、水蒸気改質反応により、水素含有ガスを生成する。 The reformer 5 generates a hydrogen-containing gas from the raw material gas by a reforming reaction. The reforming reaction may be any reforming reaction, and specifically, steam reforming reaction (steam reforming), autothermal reaction (autothermalreforming) and partial oxidation reaction (partial oxidation reforming) are exemplified. More specifically, for example, the reformer 5 includes a reforming catalyst such as a Ru catalyst or a Ni catalyst therein, and uses a raw material gas and steam supplied from a water evaporator (not shown) to reform the steam. A hydrogen-containing gas is produced by the quality reaction.

 原料ガスは、少なくとも炭素及び水素を構成元素とする有機化合物を含み、具体的には、天然ガス、都市ガス、LPG、LNG等の炭化水素が例示される。都市ガスとは、ガス会社から配管を通じて各家庭等に供給されるガスをいう。原料供給源として、これらのガスのインフラストラクチャ、及び、これらのガスを貯蔵するボンベ等が例示される。 The source gas contains at least an organic compound having carbon and hydrogen as constituent elements, and specific examples thereof include hydrocarbons such as natural gas, city gas, LPG, and LNG. City gas refers to gas supplied from a gas company to households through piping. Examples of the raw material supply source include an infrastructure of these gases and a cylinder for storing these gases.

 なお、改質器1の下流に改質器1で生成された水素含有ガス中の一酸化炭素を低減するためのCO低減器を設けても構わない。CO低減器は、シフト反応(shift reaction)により一酸化炭素を低減させる変成触媒を備える変成器と、酸化反応及びメタン化反応(methanation reaction)の少なくともいずれか一方により一酸化炭素を低減させるCO除去触媒を備えるCO除去器との少なくともいずれか一方を備える。 A CO reducer for reducing carbon monoxide in the hydrogen-containing gas produced by the reformer 1 may be provided downstream of the reformer 1. The CO reducer includes a shift converter having a shift catalyst that reduces carbon monoxide by a shift reaction, and CO removal that reduces carbon monoxide by at least one of an oxidation reaction and a methanation reaction. At least one of a CO remover including a catalyst is provided.

 原料流路1は、改質器5に供給される原料ガスが流れる流路である。図1に示す例では、原料流路1は原料ガスの供給源から改質器5に至る流路である。 The raw material flow path 1 is a flow path through which the raw material gas supplied to the reformer 5 flows. In the example shown in FIG. 1, the raw material flow path 1 is a flow path from the supply source of the raw material gas to the reformer 5.

 圧力調整器2(降圧器)は、原料流路1に設けられ、原料ガスの圧力を降下させる機能を備える。圧力調整器2には、例えば、原料ガスの圧力を機械的に低減するガバナ(governor)、及び、電気的に原料ガスの圧力を調整する比例弁(proportional valve)等が用いられる。なお、圧力調整器2は、その上流の原料ガスの圧力を、その下流の原料ガスの圧力よりも低下させることが可能であれば、いずれの構成であっても構わない。 The pressure regulator 2 (step-down device) is provided in the raw material flow path 1 and has a function of reducing the pressure of the raw material gas. For the pressure regulator 2, for example, a governor that mechanically reduces the pressure of the raw material gas, a proportional valve that electrically adjusts the pressure of the raw material gas, and the like are used. Note that the pressure regulator 2 may have any configuration as long as the pressure of the upstream source gas can be lower than the pressure of the downstream source gas.

 また、原料ガスの圧力が相対的に大きくなるほど、圧力調整器2で降下される圧力が大きくなってもよい。この場合、原料ガスの圧力が相対的に小さいと(例えば、ゲージ圧[gauge pressure]で1kPa)、圧力調整器によって、原料ガスの圧力は降下されない。 Further, the pressure dropped by the pressure regulator 2 may be increased as the pressure of the source gas is relatively increased. In this case, when the pressure of the source gas is relatively small (for example, 1 kPa in gauge pressure), the pressure of the source gas is not lowered by the pressure regulator.

 また、圧力調整器2は、原料ガスの供給圧の変動幅の上限において、リサイクル流路の下流端と接続する原料流路1における圧力が、水添脱硫に必要な水素量がリサイクル流路6を通じて該原料流路1に供給される圧力に降圧するよう構成されていてもよい。ここで、水添脱硫に必要な水素量の設定値として、例えば、原料ガスに対して供給される水素の体積比で1%以上が設定される。 In addition, the pressure regulator 2 is configured so that the pressure in the raw material flow path 1 connected to the downstream end of the recycle flow path is equal to the recycle flow path 6 at the upper limit of the fluctuation range of the supply pressure of the raw material gas. The pressure may be reduced to the pressure supplied to the raw material flow path 1 through. Here, as a set value of the amount of hydrogen necessary for hydrodesulfurization, for example, 1% or more is set as the volume ratio of hydrogen supplied to the raw material gas.

 また、圧力調整器2は、原料ガスの圧力を低下させ、かつその下流の原料ガスの圧力の変動幅を、その上流の原料ガスの圧力の変動幅よりも低下させるものであってもよい。特に、原料ガスの圧力を低下させ、所定の圧力範囲に調整する調圧器(Pressure regulator)であっても構わない。調圧器としては、ガバナ、レギュレータ(regulator)等が例示される。 Further, the pressure regulator 2 may reduce the pressure of the raw material gas and lower the fluctuation range of the pressure of the raw material gas downstream thereof than the fluctuation range of the pressure of the raw material gas upstream thereof. In particular, it may be a pressure regulator that reduces the pressure of the raw material gas and adjusts it to a predetermined pressure range. Examples of the pressure regulator include a governor and a regulator.

 原料ガスを都市ガスとし、原料ガスの供給源を都市ガスのインフラストラクチャとする場合、インフラストラクチャの供給圧は、一般に、1.0kPa以上2.5kPa以下の範囲にあることが、JIS規格により定められている。しかしながら、調圧器を用いることで、かかる変動があった場合でも、調圧器の直下における原料ガスの圧力を、例えば、0.8kPa以上1.0kPa以下の範囲に調整される。 When the source gas is city gas and the source gas supply source is city gas infrastructure, the supply pressure of the infrastructure is generally in the range of 1.0 kPa to 2.5 kPa according to JIS standards. It has been. However, by using the pressure regulator, even when such a change occurs, the pressure of the raw material gas immediately below the pressure regulator is adjusted to a range of 0.8 kPa to 1.0 kPa, for example.

 原料ガスをLPGとし、原料ガスの供給源がLPGボンベ(LPG cylinder)であるとき、LPGボンベの供給圧は、一般に、2.0kPa以上3.3kPa以下の範囲にあることが、JIS規格により定められている。ここで、調圧器を、その直下における原料ガスの圧力が、原料ガスが都市ガスであるときと同じ、例えば0.8kPa以上1.0kPa以下、に調整されるよう構成されていてもよい。これにより、異なる種類の原料ガスについて、設計が共通化される。なお、圧力調整器2の直下における原料ガスの圧力を、都市ガスとLPGガスとの間で異なる範囲になるよう構成しても構わない。 When the source gas is LPG and the source of the source gas is an LPG cylinder (LPG cylinder), the supply pressure of the LPG cylinder is generally in the range of 2.0 kPa to 3.3 kPa according to JIS standards. It has been. Here, the pressure regulator may be configured such that the pressure of the raw material gas immediately below it is adjusted to the same value as when the raw material gas is city gas, for example, 0.8 kPa to 1.0 kPa. Thereby, the design is made common to different types of source gases. In addition, you may comprise so that the pressure of the raw material gas just under the pressure regulator 2 may become a different range between city gas and LPG gas.

 昇圧器3は、原料流路1に設けられ、圧力調整器2を通過した原料ガスの圧力を上昇させる。具体的には、ブースタポンプ等が例示される。昇圧器は、その下流における原料ガスの圧力を、その上流における原料ガスの圧力よりも高くすることができれば、いずれの機器であっても構わない。 The booster 3 is provided in the raw material flow path 1 and increases the pressure of the raw material gas that has passed through the pressure regulator 2. Specifically, a booster pump or the like is exemplified. The booster may be any device as long as the pressure of the source gas downstream can be higher than the pressure of the source gas upstream.

 水添脱硫器4は、原料流路1に設けられ、圧力調整器2を通過した原料ガス中の硫黄化合物を除去する。水添脱硫器4は、水添脱硫剤を備える。この水添脱硫剤は、具体的には例えば、原料ガス中の硫黄化合物を硫化水素に変換するCoMo系触媒と、変換された硫化水素を吸着する吸着剤であるZnO系触媒及びCuZn系触媒の少なくともいずれか一方とを備える形態としてもよいし、硫黄化合物を硫化水素へ変換する機能と硫化水素を吸着する機能の両方を備えた触媒種として、Cu-Zn-Ni系、及びCu-Zn-Fe系の少なくともいずれか一方の触媒を備える形態としてもよい。 The hydrodesulfurizer 4 is provided in the raw material flow path 1 and removes sulfur compounds in the raw material gas that has passed through the pressure regulator 2. The hydrodesulfurizer 4 includes a hydrodesulfurization agent. Specifically, this hydrodesulfurization agent includes, for example, a CoMo catalyst that converts a sulfur compound in a raw material gas into hydrogen sulfide, and a ZnO catalyst and a CuZn catalyst that are adsorbents that adsorb the converted hydrogen sulfide. At least one of them may be used, and as a catalyst species having both a function of converting a sulfur compound into hydrogen sulfide and a function of adsorbing hydrogen sulfide, Cu—Zn—Ni-based and Cu—Zn— It is good also as a form provided with at least any one of Fe-type catalyst.

 硫黄化合物は、付臭成分として人為的に原料へ添加されるものであってもよいし、原料自体に由来する天然の硫黄化合物であってもよい。具体的には、ターシャリブチルメルカプタン(TBM:tertiary-butylmercaptan)、ジメチルスルフィド(DMS:dimethyl sulfide)、テトラヒドロチオフェン(THT:Tetrahydrothiophene)、硫化カルボニル(COS:carbonyl sulfide)、硫化水素(hydrogen sulfide)等が例示される。 The sulfur compound may be artificially added to the raw material as an odorous component, or may be a natural sulfur compound derived from the raw material itself. Specifically, tertiary-butylmercaptan (TBM), dimethyl sulfide (DMS), tetrahydrothiophene (THT), carbonyl sulfide (COS), hydrogen sulfide (hydrogen sulfide), etc. Is exemplified.

 また、図1に示す例では、昇圧器3が水添脱硫器4よりも上流に配置されているが、昇圧器3及び水添脱硫器4のどちらをより上流に配置するかは、任意である。 In the example shown in FIG. 1, the booster 3 is disposed upstream of the hydrodesulfurizer 4. However, it is arbitrary which of the booster 3 and the hydrodesulfurizer 4 is disposed upstream. is there.

 リサイクル流路6は、改質器5で生成された水素含有ガスを圧力調整器2よりも下流かつ水添脱硫器4及び昇圧器3よりも上流の原料流路1へと供給する流路である。リサイクル流路6を流れるガスを以下ではリサイクルガスと呼ぶ。図1の例では、リサイクル流路6は改質器5を通過した水素含有ガスが流れる流路から分岐して、圧力調整器2から昇圧器3に至るまでの原料流路1に接続される。 The recycle channel 6 is a channel for supplying the hydrogen-containing gas generated in the reformer 5 to the raw material channel 1 downstream of the pressure regulator 2 and upstream of the hydrodesulfurizer 4 and the booster 3. is there. Hereinafter, the gas flowing through the recycle channel 6 is referred to as recycle gas. In the example of FIG. 1, the recycle channel 6 branches from the channel through which the hydrogen-containing gas that has passed through the reformer 5 flows, and is connected to the raw material channel 1 from the pressure regulator 2 to the booster 3. .

 ここで、リサイクル流路6の上流端は、改質器5を通過した水素含有ガスが流れる流路であれば、いずれの箇所と接続されても構わない。例えば、改質器1の下流に上記CO低減器を設けた場合、上記上流端は、改質器1からCO低減器に至るまでの流路に接続されてもよいし、CO低減器に接続されてもよいし、CO低減器の下流の流路に接続されてもよい。なお、CO低減器が、シフト反応により一酸化炭素を低減する変成器と、酸化反応及びメタン化反応の少なくともいずれか一方により一酸化炭素を低減するCO除去器とを備える場合、リサイクル流路6の上流端を変成器とCO除去器との間の流路に接続するよう構成しても構わない。また、リサイクル流路6の上流端を、水素含有ガスを利用する水素利用機器(図示せず)の下流の流路に接続しても構わない。ここで、水素利用機器は、水素生成装置100から供給される水素含有ガスを利用する機器であり、例えば、燃料電池、または水素貯蔵容器等が例示される。 Here, the upstream end of the recycle channel 6 may be connected to any location as long as the hydrogen-containing gas that has passed through the reformer 5 flows. For example, when the CO reducer is provided downstream of the reformer 1, the upstream end may be connected to a flow path from the reformer 1 to the CO reducer, or connected to the CO reducer. Or may be connected to a flow path downstream of the CO reducer. In the case where the CO reducer includes a transformer that reduces carbon monoxide by a shift reaction and a CO remover that reduces carbon monoxide by at least one of an oxidation reaction and a methanation reaction, the recycle flow path 6 You may comprise so that the upstream end of may be connected to the flow path between a transformer and a CO remover. Moreover, you may connect the upstream end of the recycle flow path 6 to the flow path downstream of the hydrogen utilization apparatus (not shown) using hydrogen-containing gas. Here, the hydrogen-using device is a device that uses the hydrogen-containing gas supplied from the hydrogen generation apparatus 100, and examples thereof include a fuel cell and a hydrogen storage container.

 また、リサイクル流路6の下流端は、圧力調整器2よりも下流、かつ水添脱硫器4及び昇圧器3よりも上流の原料流路1へと水素含有ガスを供給可能であれば、原料流路1のいずれの箇所に設けても構わない。例えば、図1に示す例では、リサイクル流路6の下流端は、圧力調整器2から昇圧器3に至るまでの原料流路1に接続されている。しかしながら、水添脱硫器4が昇圧器3よりも上流に配置される構成では、リサイクル流路6の下流端が、圧力調整器2から水添脱硫器4に至るまでの原料流路1に接続される。 Further, the downstream end of the recycle channel 6 can be used as a raw material as long as hydrogen-containing gas can be supplied to the raw material channel 1 downstream from the pressure regulator 2 and upstream from the hydrodesulfurizer 4 and the booster 3. You may provide in any location of the flow path 1. For example, in the example shown in FIG. 1, the downstream end of the recycle flow path 6 is connected to the raw material flow path 1 from the pressure regulator 2 to the booster 3. However, in the configuration in which the hydrodesulfurizer 4 is arranged upstream of the booster 3, the downstream end of the recycle channel 6 is connected to the raw material channel 1 from the pressure regulator 2 to the hydrodesulfurizer 4. Is done.

 上述の通り、リサイクル流路6の下流端は、圧力調整器2よりも下流かつ水添脱硫器4及び昇圧器3よりも上流の原料流路1に接続されている。従って、原料ガスの供給圧が高くても、圧力調整器2の下流では圧力が低下するため、リサイクル流路の上流端と下流端との間の差圧の低下が抑制される。従って、原料ガスの供給圧が高くても、従来の水素生成装置に比べ、リサイクルガスの流量の低下が抑制される。 As described above, the downstream end of the recycle channel 6 is connected to the raw material channel 1 downstream from the pressure regulator 2 and upstream from the hydrodesulfurizer 4 and the booster 3. Therefore, even if the supply pressure of the raw material gas is high, the pressure is reduced downstream of the pressure regulator 2, so that a decrease in the differential pressure between the upstream end and the downstream end of the recycle channel is suppressed. Therefore, even if the supply pressure of the raw material gas is high, a decrease in the flow rate of the recycle gas is suppressed as compared with the conventional hydrogen generator.

 なお、原料ガスの供給圧が高いときに、リサイクル流路の上流端と下流端との差圧の低下を抑制するため、昇圧器3の出力を増加させ、リサイクル流路の上流端の圧力を高める方法もあるが、改質器5で必要以上の水素含有ガスが生成される。しかしながら、上述のように、圧力調整器2を用いると、昇圧器3の出力を増加させて必要以上の水素含有ガスを生成しなくても、差圧の低下が抑制される場合がある。 When the supply pressure of the raw material gas is high, the output of the booster 3 is increased to reduce the pressure at the upstream end of the recycling flow path in order to suppress a decrease in the differential pressure between the upstream end and the downstream end of the recycling flow path. Although there is a method of increasing the hydrogen content, the reformer 5 generates more hydrogen-containing gas than necessary. However, as described above, when the pressure regulator 2 is used, a decrease in the differential pressure may be suppressed without increasing the output of the booster 3 and generating more hydrogen gas than necessary.

 また、リサイクル流路の上流端と接続する箇所よりも下流の水素含有ガスの流路の流路抵抗を高めることで、リサイクル流路の上流端の圧力を高める方法もあるが、所定量の原料ガスを供給するのに必要な昇圧器の出力が増加する。従って、昇圧器での消費電力が増加したり、高コストになる可能性がある。しかしながら、上述のように、圧力調整器2を用いると、リサイクル流路の上流端と接続する箇所よりも下流の水素含有ガスの流路の流路抵抗の増加量を低減しても、上記差圧の低下が抑制される場合がある。つまり、昇圧器の消費電力の増加、及び昇圧器の高コスト化が抑制される。 There is also a method for increasing the pressure at the upstream end of the recycle flow path by increasing the flow resistance of the hydrogen-containing gas flow path downstream from the location connected to the upstream end of the recycle flow path. The booster output required to supply gas is increased. Therefore, there is a possibility that the power consumption in the booster increases or the cost increases. However, as described above, when the pressure regulator 2 is used, even if the increase in the channel resistance of the hydrogen-containing gas channel downstream of the portion connected to the upstream end of the recycle channel is reduced, the above difference is achieved. The pressure drop may be suppressed. That is, an increase in power consumption of the booster and an increase in cost of the booster are suppressed.

 次に、圧力調整器2が上記調圧器であると、調圧器を設けない場合に比べ、リサイクル流路の上流端と下流端との差圧の変動が抑制されるので、リサイクルガスの流量が不足したり、過剰になったりする可能性が低減する。 Next, when the pressure regulator 2 is the above-described pressure regulator, fluctuations in the differential pressure between the upstream end and the downstream end of the recycling flow path are suppressed as compared with the case where no pressure regulator is provided. The possibility of being deficient or excessive is reduced.

 例えば、原料ガスが都市ガスであって、圧力調整器2が設けられず、昇圧器3の直下におけるガス圧力が一定である場合、リサイクル流路の上流端と下流端との差圧は、1.5kPaの幅で変動することになる。その結果、リサイクルガスの流量も変動する。場合によっては、リサイクルガスの流量が水添脱硫に必要な流量に対して不足し、水添脱硫器4における脱硫が不十分となって、改質器5の改質触媒が被毒される可能性がある。また、場合によっては、リサイクルガスの流量が水添脱硫に必要な量に対して過剰になり、リサクルガスに含まれる水蒸気も過多になり、水添脱硫器4の水添脱硫剤が劣化するという可能性がある。 For example, when the source gas is city gas, the pressure regulator 2 is not provided, and the gas pressure directly below the booster 3 is constant, the differential pressure between the upstream end and the downstream end of the recycle channel is 1 It will fluctuate with a width of .5 kPa. As a result, the flow rate of the recycled gas also varies. In some cases, the flow rate of the recycle gas is insufficient with respect to the flow rate required for hydrodesulfurization, desulfurization in the hydrodesulfurizer 4 becomes insufficient, and the reforming catalyst of the reformer 5 may be poisoned. There is sex. In some cases, the flow rate of the recycle gas becomes excessive with respect to the amount required for hydrodesulfurization, the water vapor contained in the recycle gas is excessive, and the hydrodesulfurization agent of the hydrodesulfurizer 4 is deteriorated. There is sex.

 ここで、調圧器を用いると、昇圧器3の直下におけるガス圧力が一定であるとき、リサイクル流路の上流端と下流端との差圧の変動幅は、例えば、0.2kPaに低減するので、上記問題が発生する可能性が低減する。 Here, when the pressure regulator is used, when the gas pressure immediately below the booster 3 is constant, the fluctuation range of the differential pressure between the upstream end and the downstream end of the recycle flow path is reduced to, for example, 0.2 kPa. The possibility that the above problem will occur is reduced.

 (第2実施形態)
 第2実施形態の水素生成装置は、第1実施形態及びその変形例の少なくとも1つにかかる水素生成装置において、原料流路とリサイクル流路との合流部よりも上流の原料流路に、原料中の硫黄化合物を常温で除去する常温脱硫器を備え、圧力調整器は、常温脱硫器の上流の原料流路に配設されている。
(Second Embodiment)
In the hydrogen generator according to the first embodiment and the modification thereof, the hydrogen generator according to the second embodiment is provided with a raw material in the raw material channel upstream of the junction of the raw material channel and the recycle channel. A room temperature desulfurizer for removing sulfur compounds therein at room temperature is provided, and the pressure regulator is disposed in the raw material flow path upstream of the room temperature desulfurizer.

 かかる構成では、圧力調整器を常温脱硫器よりも下流で、かつ昇圧器及び水添脱硫器よりも上流の原料流路に配設した場合に比べ、原料流路とリサイクル流路との合流部よりも位置的に遠くなる。これにより、リサイクル流路を介して流入する水素含有ガスに含まれる水蒸気により圧力調整器が劣化する可能性が低減する。 In such a configuration, compared with the case where the pressure regulator is disposed in the raw material flow path downstream of the room temperature desulfurization apparatus and upstream of the booster and the hydrodesulfurization apparatus, the joining portion of the raw material flow path and the recycle flow path. The position is farther than. Thereby, possibility that a pressure regulator will deteriorate with the water vapor | steam contained in the hydrogen containing gas which flows in via a recycle channel reduces.

 図2は、第2実施形態にかかる水素生成装置の概略構成の一例を示すブロック図である。図2に示す例では、本実施形態の水素生成装置200は、常温脱硫器7を備えている。 FIG. 2 is a block diagram showing an example of a schematic configuration of the hydrogen generator according to the second embodiment. In the example shown in FIG. 2, the hydrogen generator 200 of this embodiment includes a room temperature desulfurizer 7.

 常温脱硫器7は、常温において硫黄化合物を吸着する吸着剤を備えている。吸着剤としては、例えば、活性炭及び銀ゼオライト(Ag-zeolite)等を用いることができる。ここで、常温との用語は、水添脱硫器4の使用温度(例えば、300℃前後)に比べ相対的に常温域に近いことから使用しており、常温域から使用脱硫剤が脱硫剤として有効に機能する温度までを含む意味である。 The room temperature desulfurizer 7 includes an adsorbent that adsorbs sulfur compounds at room temperature. As the adsorbent, for example, activated carbon, silver zeolite (Ag-zeolite), or the like can be used. Here, the term “normal temperature” is used because it is relatively close to the normal temperature range compared to the operating temperature of the hydrodesulfurizer 4 (for example, around 300 ° C.), and the used desulfurizing agent is used as the desulfurizing agent from the normal temperature range. It is meant to include temperatures that function effectively.

 本実施形態においては、原料流路1が圧力調整器2の下流において2つに分岐し、一方に第2開閉弁22と常温脱硫器7とが設けられ、他方に第1開閉弁21が設けられる。分岐した原料流路1は、常温脱硫器7の下流において合流し、合流部の下流において昇圧器3に接続されている。常温脱硫器7は、圧力調整器2よりも下流かつ原料流路1とリサイクル流路6との合流部よりも上流の原料流路1に設けられるが、ここでいう上流とは、少なくとも、常温脱硫器7が設けられる原料流路1が分岐する部分が、原料流路1とリサイクル流路6との合流部よりも上流にあることをいう。 In this embodiment, the raw material flow path 1 branches into two downstream of the pressure regulator 2, the second on-off valve 22 and the room temperature desulfurizer 7 are provided on one side, and the first on-off valve 21 is provided on the other side. It is done. The branched raw material flow path 1 merges downstream of the room temperature desulfurizer 7 and is connected to the booster 3 downstream of the merge portion. The room temperature desulfurizer 7 is provided in the raw material flow path 1 downstream of the pressure regulator 2 and upstream of the junction of the raw material flow path 1 and the recycle flow path 6. The upstream here refers to at least the normal temperature It means that the portion where the raw material flow path 1 where the desulfurizer 7 is provided branches is upstream of the junction of the raw material flow path 1 and the recycle flow path 6.

 第1開閉弁21と第2開閉弁22とは、圧力調整器2を通過した原料が分岐した原料流路1のうちのどちら側に流入するかを切替える切替器として機能する。第1開閉弁21及び第2開閉弁22の代わりに、三方弁等、他の切替器が用いられてもよい。 The first on-off valve 21 and the second on-off valve 22 function as a switch for switching to which side of the branched material flow path 1 the material that has passed through the pressure regulator 2 flows. Instead of the first on-off valve 21 and the second on-off valve 22, other switching devices such as a three-way valve may be used.

 図2の例では第2開閉弁22が常温脱硫器7の上流に配置されているが、第2開閉弁22が常温脱硫器7の下流に配置されていてもよい。 2, the second on-off valve 22 is disposed upstream of the room temperature desulfurizer 7, but the second on-off valve 22 may be disposed downstream of the room temperature desulfurizer 7.

 リサイクル流路6には、第3開閉弁23が設けられている。 The recycle channel 6 is provided with a third on-off valve 23.

 第1開閉弁21と第2開閉弁22と第3開閉弁23とは、例えば、電磁弁を用いることができる。 As the first on-off valve 21, the second on-off valve 22, and the third on-off valve 23, for example, electromagnetic valves can be used.

 第2実施形態の水素生成装置200において、上記以外の構成は、第1実施形態及びその変形例のいずれか1つと同様に構成できる。よって、図1と図2とで共通する構成要素については、同一の符号及び名称を付して詳細な説明を省略する。 In the hydrogen generator 200 of the second embodiment, the configuration other than the above can be configured in the same manner as that of any one of the first embodiment and its modifications. 1 and 2 are denoted by the same reference numerals and names, and detailed description thereof is omitted.

 本実施形態では、起動時及び運転停止時の少なくともいずれか一方において、改質器5に原料を供給する場合、常温脱硫器7により原料中の硫黄化合物を除去する。具体的には、圧力調整器2を通過した原料ガスが常温脱硫器7を通過するように、第1開閉弁21が閉止され、第2開閉弁22が開放される。また、第3開閉弁23は閉止される。 In this embodiment, when the raw material is supplied to the reformer 5 at least one of when starting and when the operation is stopped, the sulfur compound in the raw material is removed by the room temperature desulfurizer 7. Specifically, the first on-off valve 21 is closed and the second on-off valve 22 is opened so that the raw material gas that has passed through the pressure regulator 2 passes through the room temperature desulfurizer 7. Further, the third on-off valve 23 is closed.

 例えば、起動時では、改質器5の昇温時には常温脱硫器7を用いて脱硫を行い、その後、改質器5において水素含有ガスの生成を開始してから、第2開閉弁22が閉止され、第1開閉弁21及び第3開閉弁23が開放される。つまり、水添脱硫器4を用いた脱硫が開始される。 For example, at the time of start-up, when the temperature of the reformer 5 is increased, desulfurization is performed using the room temperature desulfurizer 7, and then the generation of hydrogen-containing gas is started in the reformer 5, and then the second on-off valve 22 is closed. Then, the first on-off valve 21 and the third on-off valve 23 are opened. That is, desulfurization using the hydrodesulfurizer 4 is started.

 なお、運転停止時においては、水素生成装置100の水素生成運転停止後、改質器5の温度低下に伴う改質器5の内圧低下またはガス収縮を補うため、改質器5に原料ガスを補給する動作を実行するが、このときに常温脱硫器7を用いて脱硫する。なお、改質器5の内圧低下は、運転停止時に改質器5の下流のガス流路が弁より閉止され、改質器5が封止されるよう構成された水素生成装置100において起こる。また、改質器5のガス収縮は、運転停止後も改質器5が大気に開放されるよう改質器5の下流のガス流路が閉止されないよう構成された水素生成装置100において起こる。 When the operation is stopped, after the hydrogen generation operation of the hydrogen generator 100 is stopped, the raw material gas is supplied to the reformer 5 in order to compensate for a decrease in internal pressure or gas contraction of the reformer 5 due to a temperature decrease of the reformer 5. The operation of replenishing is executed. At this time, desulfurization is performed using the room temperature desulfurizer 7. The internal pressure drop of the reformer 5 occurs in the hydrogen generator 100 configured so that the gas flow path downstream of the reformer 5 is closed by the valve when the operation is stopped, and the reformer 5 is sealed. Further, the gas shrinkage of the reformer 5 occurs in the hydrogen generator 100 configured so that the gas flow path downstream of the reformer 5 is not closed so that the reformer 5 is opened to the atmosphere even after the operation is stopped.

 以上の動作は、図示されない制御器により実行されうる。制御器の構成は、第4実施形態と同様としうる。 The above operations can be executed by a controller (not shown). The configuration of the controller can be the same as in the fourth embodiment.

 (第3実施形態)
 第3実施形態の水素生成装置は、第1実施形態及び第2実施形態及びそれらの変形例の少なくとも1つにかかる水素生成装置において、圧力調整器よりも上流の原料流路に、原料流路の圧力を検知する圧力検知器を備える。
(Third embodiment)
The hydrogen generator of the third embodiment is the same as that of the hydrogen generator according to at least one of the first embodiment, the second embodiment, and the modifications thereof. A pressure detector for detecting the pressure of

 かかる構成では、圧力検知器が圧力調整器よりも下流の原料流路に設けられた場合に比べ、原料ガスの供給圧の異常低下がより早期に検知される。 In such a configuration, an abnormal drop in the supply pressure of the raw material gas is detected earlier than when the pressure detector is provided in the raw material flow path downstream of the pressure regulator.

 図3は、第2実施形態にかかる水素生成装置の概略構成の一例を示すブロック図である。図3に示す例では、本実施形態の水素生成装置300は、圧力検知器8を備えている。 FIG. 3 is a block diagram showing an example of a schematic configuration of the hydrogen generator according to the second embodiment. In the example shown in FIG. 3, the hydrogen generator 300 of this embodiment includes a pressure detector 8.

 圧力検知器8は、原料流路1の圧力を検知する。具体的には例えば、ダイアフラム型の圧力センサ(diaphragm pressure censor)、ベローズ型の圧力センサ(bellows pressure censor)等を利用することで、原料流路1の内部における原料ガスの圧力を検出する。 The pressure detector 8 detects the pressure in the raw material flow path 1. Specifically, for example, the pressure of the raw material gas in the raw material flow path 1 is detected by using a diaphragm type pressure sensor (diaphragm pressure censor), a bellows type pressure sensor (bellows pressure censor), or the like.

 第3実施形態の水素生成装置300において、上記以外の構成は、第1実施形態及び第2実施形態及びそれらの変形例のいずれか1つと同様に構成できる。よって、図1と図3とで共通する構成要素については、同一の符号及び名称を付して詳細な説明を省略する。 In the hydrogen generator 300 of the third embodiment, the configuration other than the above can be configured in the same manner as any one of the first embodiment, the second embodiment, and their modifications. Therefore, components common to FIGS. 1 and 3 are given the same reference numerals and names, and detailed description thereof is omitted.

 水素生成装置300において圧力検知器8は、原料流路1の上流にある、原料ガスの供給源のガス供給圧を検知する。原料ガスの供給が何らかの原因で供給圧が異常に低下した場合、これを放置すると、水素生成装置300の故障または異常を招く可能性がある。 In the hydrogen generator 300, the pressure detector 8 detects the gas supply pressure of the source gas supply source located upstream of the source channel 1. If the supply pressure drops abnormally for some reason due to the supply of the raw material gas, if this is left unattended, there is a possibility that the hydrogen generator 300 will be broken or abnormal.

 仮に、圧力調整器2の下流は上流よりも圧力の変動幅が小さくなりやすいので、圧力調整器2の上流に比べ、原料の供給圧の異常低下を検知しにくい。そこで、圧力検知器8を圧力調整器2よりも上流の原料流路1に配置することで、圧力調整器2の影響を受けずに、原料の供給圧の変化をより早期に検知することができる。 Temporarily, since the pressure fluctuation range tends to be smaller in the downstream of the pressure regulator 2 than in the upstream, it is difficult to detect an abnormal drop in the supply pressure of the raw material compared to the upstream of the pressure regulator 2. Therefore, by arranging the pressure detector 8 in the raw material flow path 1 upstream of the pressure regulator 2, it is possible to detect the change in the supply pressure of the raw material earlier without being affected by the pressure regulator 2. it can.

 圧力検知器8により、原料の異常低下を検知した場合の、具体的な処理方法は特に限定されない。例えば、水素生成装置300の運転が停止されてもよいし、昇圧器3の動作が停止されてもよいし、原料流路1に設けられた図示されない開閉弁を閉止することで、原料ガスが昇圧器3により吸引されることが防止されてもよい。 The specific processing method in the case where the pressure detector 8 detects an abnormal decrease in the raw material is not particularly limited. For example, the operation of the hydrogen generator 300 may be stopped, the operation of the booster 3 may be stopped, or the raw material gas is changed by closing a not-illustrated on-off valve provided in the raw material flow path 1. Suction by the booster 3 may be prevented.

 本実施形態におけるリサイクル流路を流れるガスの流量制御は、第1実施形態と同様であるので、詳細な説明を省略する。 Since the flow rate control of the gas flowing through the recycle channel in the present embodiment is the same as that in the first embodiment, detailed description thereof is omitted.

 (第4実施形態)
 第4実施形態の水素生成装置は、第1実施形態ないし第3実施形態及びそれらの変形例の少なくとも1つにかかる水素生成装置において、原料流路に設けられた開閉弁と、水素生成装置での水素生成運転の停止後、改質器の温度低下に伴う改質器の内圧低下または改質器内のガス収縮に対して、開閉弁を開放するとともに、昇圧器を動作させ、改質器に原料ガスを供給する制御器とを備える。
(Fourth embodiment)
The hydrogen generator according to the fourth embodiment includes an on-off valve provided in the raw material flow path and a hydrogen generator in the hydrogen generator according to at least one of the first to third embodiments and their modifications. After stopping the hydrogen generation operation, the open / close valve is opened and the reformer is operated in response to a decrease in internal pressure of the reformer due to a decrease in the temperature of the reformer or a gas contraction in the reformer. And a controller for supplying the raw material gas.

 圧力調整器の下流のガス圧は上流よりも低くなるため、原料流路に設けられた開閉弁を開放しても改質器の下流の流路まで原料ガスが供給されず、補圧されない可能性がある。かかる構成において、開閉弁を開放するとともに昇圧器を動作させることで、改質器の下流の流路まで原料ガスが供給され、補圧される可能性が向上する。 Since the gas pressure downstream of the pressure regulator is lower than upstream, even if the on-off valve provided in the raw material flow path is opened, the raw material gas is not supplied to the downstream flow path of the reformer and cannot be supplemented. There is sex. In such a configuration, by opening the on-off valve and operating the booster, the possibility that the source gas is supplied to the flow path downstream of the reformer and supplemented is improved.

 [装置構成]
 図4は、第4実施形態にかかる水素生成装置の概略構成の一例を示すブロック図である。図4に示す例では、本実施形態の水素生成装置400は、開閉弁9と、圧力検知器13、制御器10とを備えている。
[Device configuration]
FIG. 4 is a block diagram illustrating an example of a schematic configuration of the hydrogen generator according to the fourth embodiment. In the example shown in FIG. 4, the hydrogen generator 400 of this embodiment includes the on-off valve 9, the pressure detector 13, and the controller 10.

 開閉弁9は、例えば、電磁弁を用いることができる。開閉弁9は、制御器10に通信可能に接続され、制御器10の制御に基づいて開閉される。図4に示す例において、開閉弁9は昇圧器3の下流かつ水添脱硫器4の上流の原料流路1に配設されているが、かかる構成に限定されるものではなく、開閉弁9は原料流路1であれば任意の箇所に配置されうる。 The on-off valve 9 can be a solenoid valve, for example. The on-off valve 9 is communicably connected to the controller 10 and is opened and closed based on the control of the controller 10. In the example shown in FIG. 4, the on-off valve 9 is disposed in the raw material flow path 1 downstream of the booster 3 and upstream of the hydrodesulfurizer 4, but is not limited to this configuration. Can be disposed at any location as long as it is a raw material flow path 1.

 なお、水素生成装置400の水素生成運転停止後、改質器5内部で水の蒸発が継続し、水蒸気及び高温のガス等が原料流路1に逆流する場合がある。そこで、水素生成運転停止後、開閉弁9を閉止することで、水蒸気及び高温のガス等の逆流が防止される。 In addition, after the hydrogen generation operation of the hydrogen generator 400 is stopped, the evaporation of water continues in the reformer 5, and water vapor and high-temperature gas may flow back into the raw material flow path 1. Therefore, by closing the on-off valve 9 after the hydrogen generation operation is stopped, the backflow of water vapor and high-temperature gas is prevented.

 圧力検知器13は、改質器5の内圧を検知する。 The pressure detector 13 detects the internal pressure of the reformer 5.

 制御器10は、水素生成装置400での水素生成運転の停止後、改質器5の温度低下に伴う内圧低下に対して、開閉弁9を開放するとともに、昇圧器3を動作させ、改質器5に原料を供給する(以下、補圧動作)。 After stopping the hydrogen generation operation in the hydrogen generator 400, the controller 10 opens the on-off valve 9 and operates the booster 3 in response to a decrease in internal pressure due to a decrease in the temperature of the reformer 5. The raw material is supplied to the vessel 5 (hereinafter referred to as “compensation operation”).

 制御器10は、制御機能を有するものであればよく、演算処理部(図示せず)と、制御プログラムを記憶する記憶部(図示せず)とを備える。演算処理部としては、MPU、CPUが例示される。記憶部としては、メモリが例示される。制御器は、集中制御を行う単独の制御器で構成されていてもよく、互いに協働して分散制御を行う複数の制御器で構成されていてもよい。 The controller 10 only needs to have a control function, and includes an arithmetic processing unit (not shown) and a storage unit (not shown) for storing a control program. Examples of the arithmetic processing unit include an MPU and a CPU. A memory is exemplified as the storage unit. The controller may be composed of a single controller that performs centralized control, or may be composed of a plurality of controllers that perform distributed control in cooperation with each other.

 補圧動作とは、例えば、水素生成装置の停止処理開始後に、改質器の内部温度の低下に伴い生じる圧力低下の少なくとも一部を補うように、当該改質器の内部へとガスを供給することを言う。なお、圧力調整器2よりも上流の原料の供給圧を超える量のガスが供給されてもよい。より具体的には、例えば、圧力調整器2よりも上流の原料の供給圧をP1とすると、補圧動作時に昇圧器3を動作させ、改質器5の内圧がP1よりも大きいP2以上になるように改質器5内部に原料ガスを供給する。 The supplementary pressure operation refers to, for example, supplying gas to the interior of the reformer so as to compensate for at least part of the pressure drop caused by the lowering of the internal temperature of the reformer after the hydrogen generator is stopped. Say to do. An amount of gas exceeding the supply pressure of the raw material upstream of the pressure regulator 2 may be supplied. More specifically, for example, if the supply pressure of the raw material upstream of the pressure regulator 2 is P1, the booster 3 is operated during the pressure compensation operation, and the internal pressure of the reformer 5 is set to P2 or more which is larger than P1. Thus, the raw material gas is supplied into the reformer 5.

 なお、上記改質器5内部の圧力を検知する検知器として、改質器5内部の圧力を検知する圧力検知器を用いてもよいが、改質器5内部の圧力を間接的に検知する検知器を用いても構わない。改質器5内部の圧力を間接的に検知する検知器としては、例えば、改質器の温度を検知する温度検知器、改質器5を封止してからの経過時間を計測する計時器等が挙げられる。 As a detector for detecting the pressure inside the reformer 5, a pressure detector for detecting the pressure inside the reformer 5 may be used, but the pressure inside the reformer 5 is indirectly detected. A detector may be used. Examples of the detector that indirectly detects the pressure inside the reformer 5 include a temperature detector that detects the temperature of the reformer, and a timer that measures the elapsed time since the reformer 5 was sealed. Etc.

 例えば、温度検知器を用いる場合、改質器5を封止後の改質器5の温度と内圧低下との相関関係を予め実験等で求め、この相関関係から補圧動作が必要な温度条件を記憶部に記憶しておく。そして、温度検知器により検知された検知温度が、この記憶部に記憶された温度条件を満たすと、制御器10の制御により補圧動作を実行してもよい。 For example, in the case of using a temperature detector, a correlation between the temperature of the reformer 5 after sealing the reformer 5 and a decrease in internal pressure is obtained in advance through experiments or the like, and a temperature condition that requires a pressure compensation operation from this correlation Is stored in the storage unit. Then, when the detected temperature detected by the temperature detector satisfies the temperature condition stored in the storage unit, the pressure compensation operation may be executed under the control of the controller 10.

 例えば、計時器を用いる場合、改質器5を封止後の経過時間と改質器5の内圧低下との相関関係を予め実験等で求め、この相関関係から補圧動作が必要な時間条件を記憶部に記憶しておく。そして、計時器で検知された経過時間が、この記憶部に記憶された時間条件を満たすと、制御器10の制御により補圧動作を実行してもよい。 For example, when a timer is used, a correlation between an elapsed time after sealing the reformer 5 and a decrease in the internal pressure of the reformer 5 is obtained in advance by experiments or the like, and a time condition that requires a pressure compensation operation from this correlation Is stored in the storage unit. Then, if the elapsed time detected by the timer satisfies the time condition stored in the storage unit, the pressure compensation operation may be executed under the control of the controller 10.

 第4実施形態の水素生成装置400において、上記以外の構成は、第1実施形態ないし第3実施形態及びそれらの変形例のいずれか1つと同様に構成できる。よって、図1と図4とで共通する構成要素については、同一の符号及び名称を付して詳細な説明を省略する。 In the hydrogen generator 400 of the fourth embodiment, the configuration other than the above can be configured similarly to any one of the first to third embodiments and their modifications. Therefore, components common to FIGS. 1 and 4 are given the same reference numerals and names, and detailed description thereof is omitted.

 [動作]
 図5は、第4実施形態にかかる水素生成装置の動作方法の一例を示すフローチャートである。図5に示す動作は、制御器10が水素生成装置400の各部を制御することで実行される。
[Operation]
FIG. 5 is a flowchart illustrating an example of an operation method of the hydrogen generator according to the fourth embodiment. The operation shown in FIG. 5 is executed by the controller 10 controlling each part of the hydrogen generator 400.

 水素生成運転が停止すると(スタート)、昇圧器3は停止される。また、開閉弁9及び改質器5の下流の流路に設けられた開閉弁(図示せず)も閉止され、改質器5は封止される。圧力検知器が改質器5の内圧を検知する(ステップS101)。検知された圧力が第1の圧力閾値P1以下になると(ステップS102の判定結果がYes)、開閉弁9が開放されると共に昇圧器3が動作させられ(ステップS103)、その状態が所定時間T1だけ継続される(ステップS104)。これにより、改質器5の内圧低下を補うように、原料ガスが改質器5の内部へと供給される。その後、開閉弁9が閉止され、昇圧器3の動作は停止され(ステップS104)、補圧動作が終了する(エンド)。 When the hydrogen generation operation is stopped (start), the booster 3 is stopped. Moreover, the on-off valve 9 (not shown) provided in the flow path downstream of the on-off valve 9 and the reformer 5 is also closed, and the reformer 5 is sealed. The pressure detector detects the internal pressure of the reformer 5 (step S101). When the detected pressure becomes equal to or lower than the first pressure threshold value P1 (Yes in step S102), the on-off valve 9 is opened and the booster 3 is operated (step S103), and the state is maintained for a predetermined time T1. (Step S104). As a result, the raw material gas is supplied into the reformer 5 so as to compensate for the lowering of the internal pressure of the reformer 5. Thereafter, the on-off valve 9 is closed, the operation of the booster 3 is stopped (step S104), and the pressure compensation operation ends (end).

 なお、ステップS101~S105の動作を繰り返すことで、複数回に分けて補圧動作が行われてもよい。 In addition, by repeating the operations in steps S101 to S105, the compensation operation may be performed in a plurality of times.

 所定時間T1は、改質器5の内圧低下を補うために必要な量の原料ガスが改質器5へ供給されるように設定される。なお、補圧動作の停止を、補圧動作の実行時間に代えて、圧力検知器13の検知圧力で判定してもよい。具体的には、圧力検知器13の検知圧力が第2の圧力閾値P2以上になるまで、補圧動作を継続後、停止される。 The predetermined time T1 is set so that an amount of raw material gas necessary to compensate for the decrease in internal pressure of the reformer 5 is supplied to the reformer 5. The stoppage of the supplementary pressure operation may be determined by the detected pressure of the pressure detector 13 instead of the execution time of the supplementary pressure operation. Specifically, the supplementary pressure operation is continued and stopped until the detected pressure of the pressure detector 13 becomes equal to or higher than the second pressure threshold value P2.

 [変形例]
 本変形例の水素生成装置は、第1実施形態ないし第3実施形態及びそれらの変形例の少なくとも1つにかかる水素生成装置において、原料流路に設けられた開閉弁と、水素生成装置での水素生成運転の停止後、改質器の温度低下に伴う前記改質器内のガス収縮に対して、開閉弁を開放するとともに、昇圧器を動作させ、改質器に原料ガスを供給する制御器とを備える。
[Modification]
The hydrogen generator of this modification is the same as that of the first to third embodiments and the hydrogen generator according to at least one of those modifications, in the on-off valve provided in the raw material flow path, Control of opening the on-off valve and operating the booster to supply the raw material gas to the reformer against the gas contraction in the reformer due to the temperature drop of the reformer after the hydrogen generation operation is stopped With a vessel.

 本変形例は、水素生成装置400の水素生成運転停止後、改質器5が大気に開放されるよう構成されている。具体的には、改質器5の下流の経路に開閉弁が設けられていない。 This modification is configured such that the reformer 5 is opened to the atmosphere after the hydrogen generation operation of the hydrogen generator 400 is stopped. Specifically, no on-off valve is provided in the path downstream of the reformer 5.

 従って、改質器5の温度低下に伴い改質器5内のガスが収縮し、大気開放された改質器5の下流の流路を介して空気が流入し、触媒の酸化劣化等を招く恐れがある。なお、上記触媒の酸化劣化は、改質触媒の酸化劣化、変成触媒の酸化劣化及びCO除去触媒の酸化劣化の少なくともいずれか一つを意味する。 Therefore, as the temperature of the reformer 5 decreases, the gas in the reformer 5 contracts and air flows in through the flow path downstream of the reformer 5 that is open to the atmosphere, leading to oxidative degradation of the catalyst. There is a fear. The oxidation deterioration of the catalyst means at least one of oxidation deterioration of the reforming catalyst, oxidation deterioration of the shift catalyst, and oxidation deterioration of the CO removal catalyst.

 ここで、開閉弁9を開放して改質器5に原料ガスを供給して改質器5の下流の流路からの外気の流入を抑制する方法が考えられるが、本変形例の水素生成装置は、圧力調整器2が設けられているため、圧力調整器2の下流のガス圧は上流よりも低くなる。従って、開閉弁9を開放しても改質器5の下流の流路まで原料ガスが補給されず、外気により触媒が酸化劣化する可能性がある。そこで、制御器10は、改質器5内のガス収縮を補うよう開閉弁9を開放するとともに昇圧器3を動作させる。これにより、改質器5の下流のガス流路まで原料ガスが供給され、触媒が酸化劣化する可能性が低減される。 Here, a method of opening the on-off valve 9 and supplying the raw material gas to the reformer 5 to suppress the inflow of outside air from the flow path downstream of the reformer 5 can be considered. Since the apparatus is provided with the pressure regulator 2, the gas pressure downstream of the pressure regulator 2 is lower than upstream. Therefore, even if the on-off valve 9 is opened, the raw material gas is not replenished to the flow path downstream of the reformer 5, and the catalyst may be oxidized and deteriorated by the outside air. Therefore, the controller 10 opens the on-off valve 9 and operates the booster 3 to compensate for gas contraction in the reformer 5. Thereby, the raw material gas is supplied to the gas flow path downstream of the reformer 5, and the possibility that the catalyst is oxidized and deteriorated is reduced.

 図6は、第4実施形態の変形例にかかる燃料電池システムの概略構成の一例を示すブロック図である。 FIG. 6 is a block diagram showing an example of a schematic configuration of a fuel cell system according to a modification of the fourth embodiment.

 図6に示すように、本変形例の燃料電池システムは、温度検知器14を備える。 As shown in FIG. 6, the fuel cell system of this modification includes a temperature detector 14.

 温度検知器14は、改質器5の温度を検知する。 The temperature detector 14 detects the temperature of the reformer 5.

 上記改質器5の温度を検知する検知器としては、改質器5の温度を直接的に検知する温度検知器であってもよいし、間接的に検知する検知器であってもよい。改質器5の温度を間接的に検知する検知器としては、水素生成装置400の水素生成運転を停止してからの経過時間を計測する計時器等が例示される。 The detector for detecting the temperature of the reformer 5 may be a temperature detector for directly detecting the temperature of the reformer 5 or a detector for detecting it indirectly. Examples of the detector that indirectly detects the temperature of the reformer 5 include a timer that measures an elapsed time after the hydrogen generation operation of the hydrogen generator 400 is stopped.

 なお、本変形例の水素生成装置400において、図6と図4とで同一の符号を付した構成は、第4実施形態の水素生成装置と同様であるのでその詳細な説明を省略する。 In addition, in the hydrogen generator 400 of this modification, since the structure which attached | subjected the same code | symbol in FIG. 6 and FIG. 4 is the same as that of the hydrogen generator of 4th Embodiment, the detailed description is abbreviate | omitted.

 次に、本変形例の水素生成装置400の動作について説明する。 Next, the operation of the hydrogen generator 400 of this modification will be described.

 制御器10は、水素生成装置での水素生成運転の停止後、改質器の温度低下に伴う前記改質器内のガス収縮に対して、開閉弁を開放するとともに、昇圧器を動作させ、改質器に原料ガスを供給する(以下、補給動作)。 After stopping the hydrogen generation operation in the hydrogen generator, the controller 10 opens the on-off valve and operates the booster against the gas contraction in the reformer accompanying the temperature drop of the reformer, Supply raw material gas to the reformer (hereinafter referred to as replenishment operation).

 上記補給動作のタイミングは、改質器5の温度を検知する温度検知器14の検知温度に基づき判定される。 The timing of the replenishment operation is determined based on the temperature detected by the temperature detector 14 that detects the temperature of the reformer 5.

 例えば、改質器5の温度を検知する検知器として、温度検知器14を用いる場合、水素生成装置400の水素生成運転停止後の改質器5の温度と改質器5の下流の流路からの外気の流入量との相関関係を予め実験等で求め、この相関関係から補給動作が必要な温度条件を記憶部に記憶しておく。そして、温度検知器により検知された検知温度が、この記憶部に記憶された温度条件を満たすと、制御器10の制御により補圧動作を実行してもよい。 For example, when the temperature detector 14 is used as a detector for detecting the temperature of the reformer 5, the temperature of the reformer 5 after the hydrogen generation operation of the hydrogen generator 400 is stopped and the flow path downstream of the reformer 5. A correlation with the inflow amount of outside air from is obtained in advance through experiments or the like, and a temperature condition that requires a replenishment operation is stored in the storage unit from this correlation. Then, when the detected temperature detected by the temperature detector satisfies the temperature condition stored in the storage unit, the pressure compensation operation may be executed under the control of the controller 10.

 例えば、改質器5の温度を検知する検知器として、計時器を用いる場合、水素生成装置の水素生成運転停止後の経過時間と改質器5の下流の流路からの外気の流入量との相関関係を予め実験等で求め、この相関関係から補給動作が必要な時間条件を記憶部に記憶しておく。そして、計時器で検知された経過時間が、この記憶部に記憶された時間条件を満たすと、制御器10の制御により補給動作を実行してもよい。 For example, when a timer is used as a detector for detecting the temperature of the reformer 5, the elapsed time after the hydrogen generation operation of the hydrogen generator is stopped and the inflow amount of outside air from the flow path downstream of the reformer 5. Is obtained in advance by experiments or the like, and a time condition that requires a replenishment operation is stored in the storage unit from this correlation. Then, when the elapsed time detected by the timer satisfies the time condition stored in the storage unit, the replenishment operation may be executed under the control of the controller 10.

 なお、本変形例の水素生成装置400の動作フローは、ステップS102が温度検知器14の検知温度が所定の閾値T1以上であるか否かを判定するステップである以外は、図5に示すフローと同様であるのでその説明を省略する。 The operation flow of the hydrogen generator 400 of the present modification is the flow shown in FIG. 5 except that step S102 is a step of determining whether or not the temperature detected by the temperature detector 14 is equal to or higher than a predetermined threshold T1. Since this is the same, the description thereof is omitted.

 (第5実施形態)
 第5実施形態の燃料電池システムは、第1実施形態ないし第4実施形態及びそれらの変形例の少なくとも1つにかかる水素生成装置と、水素生成装置から供給される水素含有ガスを用いて発電する燃料電池とを備える。
(Fifth embodiment)
A fuel cell system according to a fifth embodiment generates power using a hydrogen generator according to at least one of the first to fourth embodiments and their modifications, and a hydrogen-containing gas supplied from the hydrogen generator. And a fuel cell.

 かかる構成では、原料ガスの供給圧が高くても、従来の水素生成装置に比べ、リサイクル流路を流れる水素ガス流量の低下が抑制される。 In such a configuration, even if the supply pressure of the raw material gas is high, a decrease in the flow rate of the hydrogen gas flowing through the recycle channel is suppressed as compared with the conventional hydrogen generator.

 図7は、第5実施形態にかかる燃料電池システムの概略構成の一例を示すブロック図である。図7に示す例では、本実施形態の燃料電池システム500は、水素生成装置100と、燃料電池20とを備えている。 FIG. 7 is a block diagram showing an example of a schematic configuration of a fuel cell system according to the fifth embodiment. In the example shown in FIG. 7, the fuel cell system 500 of this embodiment includes a hydrogen generator 100 and the fuel cell 20.

 燃料電池20は、水素生成装置から供給される水素含有ガスを用いて発電する燃料電池である。燃料電池は、いずれの種類の燃料電池であってもよく、例えば、高分子電解質形燃料電池(PEFC)、固体酸化物形燃料電池(SOFC)、及び、りん酸形燃料電池(PAFC)等を用いることができる。高分子電解質形燃料電池の場合、燃料電池ユニットにおいて、改質器と燃料電池スタックとが別個に構成される。固体酸化物形燃料電池の場合、改質反応を実行する改質部と燃料電池部とをそれぞれ個別に有する間接内部改質型、及び、燃料電池本体内部で改質反応も行う内部改質型のいずれであってもよい。つまり、燃料電池に改質器が内蔵された形態が採用される場合があり、本発明の燃料電池は、そのような形態も含むものである。 The fuel cell 20 is a fuel cell that generates electricity using a hydrogen-containing gas supplied from a hydrogen generator. The fuel cell may be any type of fuel cell, such as a polymer electrolyte fuel cell (PEFC), a solid oxide fuel cell (SOFC), a phosphoric acid fuel cell (PAFC), etc. Can be used. In the case of a polymer electrolyte fuel cell, the reformer and the fuel cell stack are separately configured in the fuel cell unit. In the case of a solid oxide fuel cell, an indirect internal reforming type having a reforming section and a fuel cell section that perform reforming reactions individually, and an internal reforming type that also performs a reforming reaction inside the fuel cell body Any of these may be used. That is, a form in which a reformer is built in the fuel cell may be employed, and the fuel cell of the present invention includes such a form.

 第5実施形態の燃料電池システム500において、水素生成装置100は、第1実施形態ないし第4実施形態及びそれらの変形例のいずれか1つと同様に構成してもよい。図1と図7とで共通する構成要素については、同一の符号及び名称を付して詳細な説明を省略する。 In the fuel cell system 500 of the fifth embodiment, the hydrogen generator 100 may be configured in the same manner as any one of the first to fourth embodiments and their modifications. Constituent elements common to FIG. 1 and FIG. 7 are given the same reference numerals and names, and detailed descriptions thereof are omitted.

 [変形例]
 図8は、第5実施形態の変形例にかかる燃料電池システムの概略構成の一例を示すブロック図である。本変形例は、燃料電池として固体酸化物形燃料電池(SOFC)を採用した構成である。
[Modification]
FIG. 8 is a block diagram illustrating an example of a schematic configuration of a fuel cell system according to a modification of the fifth embodiment. In this modification, a solid oxide fuel cell (SOFC) is adopted as the fuel cell.

 図8に示す例では、本変形例の燃料電池システム500Aは、水素生成装置100と、蒸発器11と、空気供給器12と、燃料電池本体30とを備えている。 In the example shown in FIG. 8, the fuel cell system 500 </ b> A of the present modification includes a hydrogen generator 100, an evaporator 11, an air supplier 12, and a fuel cell main body 30.

 蒸発器11は、水供給源から供給される水を蒸発させ、得られた水蒸気を改質器5へと供給する。 The evaporator 11 evaporates the water supplied from the water supply source, and supplies the obtained water vapor to the reformer 5.

 空気供給器12は、酸化剤ガスとしての空気を燃料電池本体30へと供給する。 The air supplier 12 supplies air as an oxidant gas to the fuel cell main body 30.

 燃料電池本体30は、燃料電池セルスタックであって、改質器5から供給される水素と空気供給器12から供給される空気とを用いて発電する。 The fuel cell main body 30 is a fuel cell stack, and generates electricity using hydrogen supplied from the reformer 5 and air supplied from the air supplier 12.

 改質器5と蒸発器11と燃料電池本体30とはホットモジュール40(hot module)を構成する。ホットモジュール40は一体としてその全体が加熱される。 The reformer 5, the evaporator 11, and the fuel cell body 30 constitute a hot module 40. The entire hot module 40 is heated as a whole.

 本変形例の燃料電池システム500Aにおいて、水素生成装置100は、第1実施形態ないし第4実施形態及びそれらの変形例のいずれか1つと同様に構成してもよい。図1と図8とで共通する構成要素については、同一の符号及び名称を付して詳細な説明を省略する。 In the fuel cell system 500A of the present modification, the hydrogen generator 100 may be configured in the same manner as any one of the first to fourth embodiments and their modifications. Constituent elements common to FIG. 1 and FIG. 8 are denoted by the same reference numerals and names, and detailed description thereof is omitted.

 なお、図8に示す例では、リサイクル流路6が改質器5と燃料電池本体30とを接続する流路から分岐しているが、必ずしもかかる構成に限定されず、いずれの部位から水素含有ガスが取り出されてもよい。例えば、リサイクル流路6のガス入口が燃料電池本体30から排出されるオフ燃料ガスが流れる流路と接続され、オフ燃料ガスがリサイクルガスとして圧力調整器2から昇圧器3に至る原料流路1に供給されてもよい。 In the example shown in FIG. 8, the recycle flow path 6 is branched from the flow path connecting the reformer 5 and the fuel cell main body 30. However, the recycle flow path 6 is not necessarily limited to such a configuration. Gas may be removed. For example, the gas inlet of the recycle flow path 6 is connected to the flow path through which off-fuel gas discharged from the fuel cell main body 30 flows, and the off-fuel gas is recycled gas from the pressure regulator 2 to the booster 3. May be supplied.

 上記説明から、当業者にとっては、本発明の多くの改良や他の実施形態が明らかである。従って、上記説明は、例示としてのみ解釈されるべきであり、本発明を実行する最良の態様を当業者に教示する目的で提供されたものである。本発明の精神を逸脱することなく、その構造及び/又は機能の詳細を実質的に変更できる。 From the above description, many modifications and other embodiments of the present invention are apparent to persons skilled in the art. Accordingly, the foregoing description should be construed as illustrative only and is provided for the purpose of teaching those skilled in the art the best mode of carrying out the invention. The details of the structure and / or function may be substantially changed without departing from the spirit of the invention.

 本発明の水素生成装置、及び燃料電池システムは、原料ガスの供給圧が高くても、従来の水素生成装置に比べ、リサイクル流路を流れる水素ガス流量の低下が抑制される水素生成装置及び燃料電池システムとして有用である。 The hydrogen generator and fuel cell system of the present invention are capable of suppressing a decrease in the flow rate of the hydrogen gas flowing through the recycle flow path as compared with the conventional hydrogen generator even when the supply pressure of the raw material gas is high. It is useful as a battery system.

 1 原料流路
 2 圧力調整器
 3 昇圧器
 4 水添脱硫器
 5 改質器
 6 リサイクル流路
 7 常温脱硫器
 8 圧力検知器
 9 開閉弁
 10 制御器
 11 蒸発器
 12 空気供給器
 13 圧力検知器
 14 温度検知器
 20 燃料電池
 21 第1開閉弁
 22 第2開閉弁
 23 第3開閉弁
 30 燃料電池本体
 40 ホットモジュール
 100 水素生成装置
 200 水素生成装置
 300 水素生成装置
 400 水素生成装置
 500 燃料電池システム
DESCRIPTION OF SYMBOLS 1 Raw material flow path 2 Pressure regulator 3 Booster 4 Hydrodesulfurizer 5 Reformer 6 Recycle flow path 7 Room temperature desulfurizer 8 Pressure detector 9 On-off valve 10 Controller 11 Evaporator 12 Air supply device 13 Pressure detector 14 Temperature detector 20 Fuel cell 21 First on-off valve 22 Second on-off valve 23 Third on-off valve 30 Fuel cell main body 40 Hot module 100 Hydrogen generator 200 Hydrogen generator 300 Hydrogen generator 400 Hydrogen generator 500 Fuel cell system

Claims (6)

 原料ガスから水素含有ガスを生成する改質器と、
 前記改質器に供給される原料ガスが流れる原料流路と、
 前記原料流路に設けられ、原料ガスの圧力を降下させる圧力調整器と、
 前記原料流路に設けられ、前記圧力調整器を通過した原料ガスの圧力を上昇させる昇圧器と、
 前記原料流路に設けられ、前記圧力調整器を通過した原料ガス中の硫黄化合物を除去する水添脱硫器と、
 前記改質器で生成された水素含有ガスを前記圧力調整器よりも下流かつ前記水添脱硫器及び前記昇圧器よりも上流の前記原料流路へと供給するリサイクル流路と、を備える、水素生成装置。
A reformer that generates a hydrogen-containing gas from the source gas;
A raw material flow path through which the raw material gas supplied to the reformer flows;
A pressure regulator provided in the raw material flow path for reducing the pressure of the raw material gas;
A booster that is provided in the raw material flow path and increases the pressure of the raw material gas that has passed through the pressure regulator;
A hydrodesulfurizer that is provided in the raw material flow path and removes sulfur compounds in the raw material gas that has passed through the pressure regulator;
A recycle flow path for supplying the hydrogen-containing gas generated in the reformer to the raw material flow path downstream of the pressure regulator and upstream of the hydrodesulfurizer and the booster. Generator.
 前記原料流路と前記リサイクル流路との合流部よりも上流の前記原料流路に、前記原料ガス中の硫黄化合物を常温で除去する常温脱硫器を備え、前記圧力調整器は、前記常温脱硫器の上流に配設される、請求項1記載の水素生成装置。 The raw material flow channel upstream of the joining portion of the raw material flow channel and the recycling flow channel is provided with a normal temperature desulfurizer that removes sulfur compounds in the raw material gas at normal temperature, and the pressure regulator is the normal temperature desulfurization The hydrogen generator of Claim 1 arrange | positioned upstream of a vessel.  前記圧力調整器よりも上流の前記原料流路に、前記原料流路の圧力を検知する圧力検知器を備える、請求項1または2記載の水素生成装置。 The hydrogen generator according to claim 1 or 2, further comprising a pressure detector that detects a pressure of the raw material flow channel in the raw material flow channel upstream of the pressure regulator.  前記原料流路に設けられた開閉弁と、前記水素生成装置での水素生成運転の停止後、前記改質器の温度低下に伴う前記改質器の内圧低下に対して、前記開閉弁を開放するとともに、前記昇圧器を動作させ、前記改質器に原料を供給する制御器とを備える、請求項1-3のいずれかに記載の水素生成装置。 The on-off valve provided in the raw material flow path and the on-off valve are opened in response to a decrease in the internal pressure of the reformer accompanying a decrease in temperature of the reformer after the hydrogen generation operation in the hydrogen generator is stopped. The hydrogen generator according to claim 1, further comprising a controller that operates the booster and supplies a raw material to the reformer.  前記原料流路に設けられた開閉弁と、前記水素生成装置での水素生成運転の停止後、前記改質器の温度低下に伴う前記改質器内のガス収縮に対して、前記開閉弁を開放するとともに、前記昇圧器を動作させ、前記改質器に原料を供給する制御器とを備える、請求項1-3のいずれかに記載の水素生成装置。 The on-off valve provided in the raw material flow path and the on-off valve against gas contraction in the reformer accompanying a temperature drop of the reformer after the hydrogen generation operation in the hydrogen generator is stopped. The hydrogen generator according to claim 1, further comprising: a controller that opens and operates the booster to supply a raw material to the reformer.  請求項1-5のいずれかに記載の水素生成装置と、前記水素生成装置から供給される水素含有ガスを用いて発電する燃料電池とを備える、燃料電池システム。 A fuel cell system comprising: the hydrogen generator according to any one of claims 1 to 5; and a fuel cell that generates electric power using a hydrogen-containing gas supplied from the hydrogen generator.
PCT/JP2012/004017 2011-06-30 2012-06-21 Hydrogen generation device and fuel cell system Ceased WO2013001753A1 (en)

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