WO2019049629A1 - 発電システム - Google Patents
発電システム Download PDFInfo
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- WO2019049629A1 WO2019049629A1 PCT/JP2018/030448 JP2018030448W WO2019049629A1 WO 2019049629 A1 WO2019049629 A1 WO 2019049629A1 JP 2018030448 W JP2018030448 W JP 2018030448W WO 2019049629 A1 WO2019049629 A1 WO 2019049629A1
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- gas
- carbon dioxide
- concentration
- methane
- mixed gas
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F02—COMBUSTION ENGINES; HOT-GAS OR COMBUSTION-PRODUCT ENGINE PLANTS
- F02D—CONTROLLING COMBUSTION ENGINES
- F02D19/00—Controlling engines characterised by their use of non-liquid fuels, pluralities of fuels, or non-fuel substances added to the combustible mixtures
- F02D19/06—Controlling engines characterised by their use of non-liquid fuels, pluralities of fuels, or non-fuel substances added to the combustible mixtures peculiar to engines working with pluralities of fuels, e.g. alternatively with light and heavy fuel oil, other than engines indifferent to the fuel consumed
- F02D19/0639—Controlling engines characterised by their use of non-liquid fuels, pluralities of fuels, or non-fuel substances added to the combustible mixtures peculiar to engines working with pluralities of fuels, e.g. alternatively with light and heavy fuel oil, other than engines indifferent to the fuel consumed characterised by the type of fuels
- F02D19/0642—Controlling engines characterised by their use of non-liquid fuels, pluralities of fuels, or non-fuel substances added to the combustible mixtures peculiar to engines working with pluralities of fuels, e.g. alternatively with light and heavy fuel oil, other than engines indifferent to the fuel consumed characterised by the type of fuels at least one fuel being gaseous, the other fuels being gaseous or liquid at standard conditions
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
- C10L3/00—Gaseous fuels; Natural gas; Synthetic natural gas obtained by processes not covered by subclass C10G, C10K; Liquefied petroleum gas
- C10L3/06—Natural gas; Synthetic natural gas obtained by processes not covered by C10G, C10K3/02 or C10K3/04
- C10L3/10—Working-up natural gas or synthetic natural gas
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
- B01D53/22—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by diffusion
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- B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
- B01D53/22—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by diffusion
- B01D53/229—Integrated processes (Diffusion and at least one other process, e.g. adsorption, absorption)
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
- C10L3/00—Gaseous fuels; Natural gas; Synthetic natural gas obtained by processes not covered by subclass C10G, C10K; Liquefied petroleum gas
- C10L3/06—Natural gas; Synthetic natural gas obtained by processes not covered by C10G, C10K3/02 or C10K3/04
- C10L3/10—Working-up natural gas or synthetic natural gas
- C10L3/101—Removal of contaminants
- C10L3/102—Removal of contaminants of acid contaminants
- C10L3/104—Carbon dioxide
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- F02D19/00—Controlling engines characterised by their use of non-liquid fuels, pluralities of fuels, or non-fuel substances added to the combustible mixtures
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- F02D19/02—Controlling engines characterised by their use of non-liquid fuels, pluralities of fuels, or non-fuel substances added to the combustible mixtures peculiar to engines working with gaseous fuels
- F02D19/021—Control of components of the fuel supply system
- F02D19/022—Control of components of the fuel supply system to adjust the fuel pressure, temperature or composition
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- F02D19/00—Controlling engines characterised by their use of non-liquid fuels, pluralities of fuels, or non-fuel substances added to the combustible mixtures
- F02D19/06—Controlling engines characterised by their use of non-liquid fuels, pluralities of fuels, or non-fuel substances added to the combustible mixtures peculiar to engines working with pluralities of fuels, e.g. alternatively with light and heavy fuel oil, other than engines indifferent to the fuel consumed
- F02D19/0626—Measuring or estimating parameters related to the fuel supply system
- F02D19/0634—Determining a density, viscosity, composition or concentration
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- F02M—SUPPLYING COMBUSTION ENGINES IN GENERAL WITH COMBUSTIBLE MIXTURES OR CONSTITUENTS THEREOF
- F02M21/00—Apparatus for supplying engines with non-liquid fuels, e.g. gaseous fuels stored in liquid form
- F02M21/02—Apparatus for supplying engines with non-liquid fuels, e.g. gaseous fuels stored in liquid form for gaseous fuels
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- F02M—SUPPLYING COMBUSTION ENGINES IN GENERAL WITH COMBUSTIBLE MIXTURES OR CONSTITUENTS THEREOF
- F02M21/00—Apparatus for supplying engines with non-liquid fuels, e.g. gaseous fuels stored in liquid form
- F02M21/02—Apparatus for supplying engines with non-liquid fuels, e.g. gaseous fuels stored in liquid form for gaseous fuels
- F02M21/0203—Apparatus for supplying engines with non-liquid fuels, e.g. gaseous fuels stored in liquid form for gaseous fuels characterised by the type of gaseous fuel
- F02M21/0215—Mixtures of gaseous fuels; Natural gas; Biogas; Mine gas; Landfill gas
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- F02M21/00—Apparatus for supplying engines with non-liquid fuels, e.g. gaseous fuels stored in liquid form
- F02M21/02—Apparatus for supplying engines with non-liquid fuels, e.g. gaseous fuels stored in liquid form for gaseous fuels
- F02M21/0218—Details on the gaseous fuel supply system, e.g. tanks, valves, pipes, pumps, rails, injectors or mixers
- F02M21/0227—Means to treat or clean gaseous fuels or fuel systems, e.g. removal of tar, cracking, reforming or enriching
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
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- F02M—SUPPLYING COMBUSTION ENGINES IN GENERAL WITH COMBUSTIBLE MIXTURES OR CONSTITUENTS THEREOF
- F02M25/00—Engine-pertinent apparatus for adding non-fuel substances or small quantities of secondary fuel to combustion-air, main fuel or fuel-air mixture
- F02M25/022—Adding fuel and water emulsion, water or steam
- F02M25/032—Producing and adding steam
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2256/00—Main component in the product gas stream after treatment
- B01D2256/24—Hydrocarbons
- B01D2256/245—Methane
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
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- B01D2257/00—Components to be removed
- B01D2257/30—Sulfur compounds
- B01D2257/304—Hydrogen sulfide
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
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- B01D2257/00—Components to be removed
- B01D2257/50—Carbon oxides
- B01D2257/504—Carbon dioxide
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- B—PERFORMING OPERATIONS; TRANSPORTING
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- B01D2257/00—Components to be removed
- B01D2257/55—Compounds of silicon, phosphorus, germanium or arsenic
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2258/00—Sources of waste gases
- B01D2258/05—Biogas
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
- C10L2270/00—Specifically adapted fuels
- C10L2270/04—Specifically adapted fuels for turbines, planes, power generation
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
- C10L2290/00—Fuel preparation or upgrading, processes or apparatus therefore, comprising specific process steps or apparatus units
- C10L2290/02—Combustion or pyrolysis
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
- C10L2290/00—Fuel preparation or upgrading, processes or apparatus therefore, comprising specific process steps or apparatus units
- C10L2290/24—Mixing, stirring of fuel components
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
- C10L2290/00—Fuel preparation or upgrading, processes or apparatus therefore, comprising specific process steps or apparatus units
- C10L2290/26—Composting, fermenting or anaerobic digestion fuel components or materials from which fuels are prepared
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
- C10L2290/00—Fuel preparation or upgrading, processes or apparatus therefore, comprising specific process steps or apparatus units
- C10L2290/54—Specific separation steps for separating fractions, components or impurities during preparation or upgrading of a fuel
- C10L2290/548—Membrane- or permeation-treatment for separating fractions, components or impurities during preparation or upgrading of a fuel
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
- C10L2290/00—Fuel preparation or upgrading, processes or apparatus therefore, comprising specific process steps or apparatus units
- C10L2290/58—Control or regulation of the fuel preparation of upgrading process
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
- C10L2290/00—Fuel preparation or upgrading, processes or apparatus therefore, comprising specific process steps or apparatus units
- C10L2290/60—Measuring or analysing fractions, components or impurities or process conditions during preparation or upgrading of a fuel
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
- C10L3/00—Gaseous fuels; Natural gas; Synthetic natural gas obtained by processes not covered by subclass C10G, C10K; Liquefied petroleum gas
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- C10L3/102—Removal of contaminants of acid contaminants
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- F02B—INTERNAL-COMBUSTION PISTON ENGINES; COMBUSTION ENGINES IN GENERAL
- F02B43/00—Engines characterised by operating on gaseous fuels; Plants including such engines
- F02B43/10—Engines or plants characterised by use of other specific gases, e.g. acetylene, oxyhydrogen
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
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- F02D—CONTROLLING COMBUSTION ENGINES
- F02D29/00—Controlling engines, such controlling being peculiar to the devices driven thereby, the devices being other than parts or accessories essential to engine operation, e.g. controlling of engines by signals external thereto
- F02D29/06—Controlling engines, such controlling being peculiar to the devices driven thereby, the devices being other than parts or accessories essential to engine operation, e.g. controlling of engines by signals external thereto peculiar to engines driving electric generators
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- F02—COMBUSTION ENGINES; HOT-GAS OR COMBUSTION-PRODUCT ENGINE PLANTS
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- F02D41/00—Electrical control of supply of combustible mixture or its constituents
- F02D41/0025—Controlling engines characterised by use of non-liquid fuels, pluralities of fuels, or non-fuel substances added to the combustible mixtures
- F02D41/0027—Controlling engines characterised by use of non-liquid fuels, pluralities of fuels, or non-fuel substances added to the combustible mixtures the fuel being gaseous
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M8/00—Fuel cells; Manufacture thereof
- H01M8/06—Combination of fuel cells with means for production of reactants or for treatment of residues
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02C—CAPTURE, STORAGE, SEQUESTRATION OR DISPOSAL OF GREENHOUSE GASES [GHG]
- Y02C20/00—Capture or disposal of greenhouse gases
- Y02C20/40—Capture or disposal of greenhouse gases of CO2
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
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- Y02E60/30—Hydrogen technology
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
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- Y02T—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO TRANSPORTATION
- Y02T10/00—Road transport of goods or passengers
- Y02T10/10—Internal combustion engine [ICE] based vehicles
- Y02T10/12—Improving ICE efficiencies
Definitions
- the present invention relates to a gas engine which generates kinetic energy by consuming a fuel gas containing carbon dioxide mainly containing methane and generating kinetic energy, and a power generation system comprising a generator driven by the kinetic energy generated by the gas engine and generating electric power.
- the present invention relates to a power generation system using, as a fuel gas, a mixed gas mainly composed of methane and carbon dioxide derived from biogas generated by methane fermentation of organic matter such as biomass and organic waste.
- biogas obtained by methane fermentation of organic wastes such as biomass and sewage sludge has attracted attention as a new energy source.
- the biogas is used in applications such as power generation or boilers as a substitute for fossil fuels.
- Biogas is mainly composed of methane and carbon dioxide, and the concentration of methane is about 50% to 75% and the concentration of carbon dioxide is about 25% to 50% depending on the production conditions (fermentation conditions) of methane gas and the species of raw materials. Can vary. In addition, it contains a slight amount of a sulfur compound such as siloxane and hydrogen sulfide, and needs to be removed at the time of use.
- a sulfur compound such as siloxane and hydrogen sulfide
- a gas engine fueled by a mixed gas mainly composed of methane such as biogas it is assumed that a biogas engine assuming that biogas is used directly as fuel and natural gas as fuel are used. Natural gas engine. In order to use biogas as a fuel for a natural gas engine, it is necessary to reduce the carbon dioxide concentration in the biogas in advance in order to raise the purity of methane to about 90% or more. Further, in the case of a biogas engine, the carbon dioxide concentration in the mixed gas is set, for example, to about 35% to 40% as a specification value.
- biogas power generation that controls the total number of gas engines to be driven and driving of an excess gas combustion apparatus according to the following Patent Document 1 An apparatus is disclosed.
- Patent Document 2 after carbon dioxide and hydrogen sulfide in biogas are absorbed and separated using an alkali absorbing solution to purify the biogas, the methane concentration is stably increased to 90% or more.
- a power generation system which is used as a fuel for an engine-type power generation device using a waste engine or a gas turbine, or a fuel cell-type power generation device using a fuel cell.
- carbon dioxide concentration and methane concentration of the mixed gas obtained are necessarily stable even if carbon dioxide is removed or separated at a constant carbon dioxide removal rate for biogas in which carbon dioxide concentration and methane concentration greatly fluctuate.
- the fluctuation of the methane concentration causes a reduction in the service life of the engine.
- the present invention has been made in view of the above-mentioned problems, and an object thereof is to provide a fuel gas containing carbon dioxide mainly containing methane to an engine to generate electric power, thereby generating carbon dioxide concentration of the fuel gas. It is an object of the present invention to provide a power generation system capable of prolonging the life of the engine by reducing the load on the engine by suppressing the fluctuation of the methane concentration.
- a power generation system comprises a gas engine generating kinetic energy by consuming a fuel gas containing carbon dioxide mainly composed of methane and a generator driven by the kinetic energy generated by the gas engine to generate electric power.
- the concentration of at least one target component gas of methane and carbon dioxide in the mixed gas relative to the mixed gas mainly composed of methane and carbon dioxide supplied from the outside
- a fuel gas supply device for controlling the concentration of the target component gas in the fuel gas of the gas engine within the setting range and supplying the gas gas as the fuel gas, carbon dioxide concentration and methane concentration of the mixed gas
- a gas concentration sensor that measures the concentration of at least one of
- the fuel gas supply device includes a carbon dioxide removal device that removes carbon dioxide in the mixed gas, and an operating condition control device that controls operating conditions that affect the increase and decrease of the carbon dioxide removal rate of the carbon dioxide removal device.
- the gas concentration sensor is disposed at least one of a front stage and a rear stage of the carbon dioxide removal apparatus,
- the operation condition control device controls the concentration of methane and carbon dioxide in the mixed gas by controlling the operation condition of the carbon dioxide removal device based on the measurement result of the gas concentration sensor. It is characterized by 1.
- the carbon dioxide of the carbon dioxide removal device Since it is possible to control to increase or decrease the removal rate according to the concentration change, a mixed gas whose methane concentration or carbon dioxide concentration is controlled within the set range according to the gas engine used is supplied to the gas engine as fuel gas. Therefore, even if the above-mentioned concentration fluctuation of the mixed gas supplied from the outside is large, the load on the gas engine can be greatly reduced, and the life of the gas engine can be prolonged.
- the mixed gas is stably supplied at a certain carbon dioxide concentration and methane concentration, and the carbon dioxide removal device removes carbon dioxide at a certain carbon dioxide removal rate with respect to the mixed gas to obtain carbon dioxide.
- the concentration of the mixed gas is reduced by decreasing the concentration, increasing the methane concentration, controlling at least one of the carbon dioxide concentration and the methane concentration within the setting range of the gas engine, and operating the gas engine stably.
- the operating condition control device controls the operating conditions of the carbon dioxide removal apparatus to increase the carbon dioxide removal rate, thereby increasing the carbon dioxide concentration of the mixed gas.
- the stable gas engine operation described above can be maintained.
- the operating condition control device controls the operating conditions of the carbon dioxide removal device to lower the carbon dioxide removal rate, similarly, The stable gas engine operation described above can be maintained.
- concentration measurement or concentration control is also possible. Therefore, it is not always necessary to perform concentration measurement and concentration control separately by using both carbon dioxide and methane as target component gases, but performing concentration measurement and concentration control separately by using both as target component gases. May be
- the concentration sensor for at least one of the carbon dioxide concentration and the methane concentration, either before or after the concentration of the target component gas is controlled within the set range in the fuel gas supply device. It may be one or both mixed gas.
- the carbon dioxide removal device selectively separates carbon dioxide contained in the mixed gas with respect to methane, and A first processing chamber and a second processing chamber separated by the carbon dioxide separation membrane;
- the first receiving port for receiving the mixed gas into the first processing chamber and the mixed gas in the first processing chamber in which the concentration of the target component gas is controlled are discharged as the fuel gas into the first processing chamber.
- a first outlet is provided,
- the second processing chamber is provided with a second discharge port for discharging the gas that has permeated from the first processing chamber to the second processing chamber via the carbon dioxide separation membrane,
- the pressure in the second processing chamber, the ambient temperature of the carbon dioxide separation membrane, and at least one of the control target operating condition candidates including the membrane area of the carbon dioxide separation membrane are based on the measurement result of the gas concentration sensor Control is a second feature.
- the second processing chamber has a second receiving port for receiving a sweep gas into the second processing chamber
- the carbon dioxide separation membrane is The gas having passed through the first processing chamber to the second processing chamber and the sweep gas are discharged from the second discharge port via the first processing chamber, and the control target operation condition candidate is set in the second processing chamber.
- a third feature is that the flow rate of the supplied sweep gas is included.
- the operating condition control device controls the operating conditions of the carbon dioxide removal device to increase or decrease the carbon dioxide removal rate by the plurality of operations of the carbon dioxide separation membrane as described above.
- one or two or more can be used in combination according to the degree of fluctuation of carbon dioxide concentration and methane concentration, and more accurate control of carbon dioxide concentration and methane concentration becomes possible. .
- a carbon dioxide carrier is added to which the carbon dioxide separation membrane selectively reacts with carbon dioxide without reacting with methane.
- the "carbon dioxide carrier” is a substance having an effect that the membrane permeation rate of carbon dioxide is promoted by the facilitated transport mechanism by containing the substance constituting the carrier in the membrane.
- the carbon dioxide carrier in the facilitated transport film selectively reacts with carbon dioxide in the mixed gas to selectively separate carbon dioxide from methane. It enables efficient separation of methane and carbon dioxide. That is, it is possible to efficiently lower the carbon dioxide concentration of the mixed gas and increase the methane concentration.
- the energy generated when the carbon dioxide reacts with the carrier is used for the energy for the carrier to release the carbon dioxide, so it is not necessary to supply the energy from the outside, and energy saving is essentially achieved. Because of this, energy saving of concentration control for methane and carbon dioxide in the mixed gas can be achieved.
- the carbon dioxide separation membrane enables efficient carbon dioxide separation with a small membrane area, particularly in the case of a facilitated transport membrane, the device can be miniaturized compared to other carbon dioxide removal devices. As a result, the entire power generation system can be miniaturized.
- water vapor is contained in at least one of the mixed gas supplied into the first processing chamber and the sweep gas supplied into the second processing chamber. Is preferred. However, if the sweep gas contains water vapor, it is limited to the case where the sweep gas has the third feature. As a result, the water necessary for the carbon dioxide facilitated transport mechanism is secured in the membrane, so that the original performance as the facilitated transport membrane is exhibited.
- a fifth feature is to provide a steam supply unit for supplying steam to one of the target gases.
- the target gas includes the sweep gas
- the present invention is limited to the case where the target gas has the third feature.
- the water necessary for the carbon dioxide facilitated transport mechanism is secured in the membrane, so the original performance as the facilitated transport membrane is exhibited.
- the operating condition control device controls the amount of water vapor addition from the water vapor supply unit to the target gas as one of the control object operating condition candidates. Thereby, control of the relative humidity of the target gas can be easily performed.
- the water vapor supply unit supplies water vapor generated by heating water by heat exchange with the high temperature exhaust gas discharged from the gas engine to the target gas.
- the water vapor supply unit supplies the water vapor contained in the exhaust gas discharged from the gas engine to the target gas.
- the mixed gas includes a gas derived from biogas generated by methane fermentation of an organic substance, and is included in the mixed gas.
- the sixth feature of the present invention is to provide a desulfurization apparatus using a super high-order desulfurization catalyst that removes sulfur components.
- the influence of the sulfur component contained in the mixed gas on the carbon dioxide carrier can be eliminated in advance, the original performance as the facilitated transport film is maintained.
- the concentration of the target component gas is lower than the set range, or A first gas supply device for supplying a first concentration adjusting gas mainly composed of methane to the mixed gas, wherein the concentration of the target component gas is higher than the setting range when the target component gas is methane; If the target component gas is carbon dioxide and the concentration of the target component gas of the mixed gas is higher than the setting range, or the first gas supply device determines that the target component gas is carbon dioxide based on the measurement result of the gas concentration sensor When the component gas is methane and the concentration of the target component gas of the mixed gas is lower than the set range, the first concentration adjusting gas is supplied to the mixed gas, and methane and carbon dioxide in the mixed gas are supplied.
- the seventh feature is to control the concentration.
- the operation condition control device Control of the operating conditions of the carbon dioxide removal apparatus alone can not sufficiently cope with the concentration fluctuation, and when it is difficult to control the carbon dioxide concentration or the methane concentration within the set range, further, the operating condition control device or carbon dioxide Even if the removal device does not function for any reason, supplying the first concentration adjusting gas to the mixed gas makes it possible to directly suppress the decrease in the methane concentration and the increase in the carbon dioxide concentration. It is possible to control the carbon dioxide concentration or the methane concentration within the set range.
- the first gas supply device further includes a second carbon dioxide removal device that selectively separates carbon dioxide contained in the mixed gas with respect to methane; It is preferable to further comprise: a first container for storing the first concentration adjusting gas prepared in advance by separating carbon dioxide from the mixed gas by using the carbon dioxide removing device of No. 2.
- the first concentration adjustment gas can be prepared in advance using a mixed gas supplied from the outside to the fuel gas supply device, so high purity methane gas such as natural gas is separately prepared for the first concentration adjustment gas. There is no need.
- the concentration of the target component gas is higher than the set range, or A second gas for supplying carbon dioxide or a second concentration adjusting gas mainly composed of methane and carbon dioxide to the mixed gas, wherein the concentration of the target component gas is lower than the setting range when the target component gas is methane; Equipped with a feeding device,
- the second gas supply device may be based on the measurement result of the gas concentration sensor, or the target
- An eighth feature is to supply the second concentration adjusting gas to the mixed gas when the component gas is methane and the concentration of the target component gas of the mixed gas is higher than the set range.
- the operation condition control device Control of the operating conditions of the carbon dioxide removal apparatus alone can not sufficiently cope with the concentration fluctuation, and when it is difficult to control the carbon dioxide concentration or the methane concentration within the set range, further, the operating condition control device or carbon dioxide Even if the removal device does not function for any reason, it is possible to directly suppress the increase in the methane concentration and the decrease in the carbon dioxide concentration by supplying the second concentration adjusting gas to the mixed gas, It is possible to control the carbon dioxide concentration or the methane concentration within the set range.
- the second gas supply device includes a second container for storing the second concentration adjusting gas, and the second concentration adjusting gas is generated by the carbon dioxide removing device. It is preferred to include carbon dioxide removed from the gas mixture. Thereby, the carbon dioxide removal device can recycle carbon dioxide removed from the mixed gas, and it is not necessary to separately prepare carbon dioxide for the second concentration adjusting gas. In addition, in the case where carbon dioxide removed from the mixed gas by the carbon dioxide removal apparatus partially contains methane contained in the mixed gas, effective use of the methane can also be achieved.
- a power generation system comprises a gas engine generating kinetic energy by consuming a fuel gas containing carbon dioxide mainly composed of methane and a generator driven by the kinetic energy generated by the gas engine to generate electric power.
- the concentration of at least one target component gas of methane and carbon dioxide in the mixed gas relative to the mixed gas mainly composed of methane and carbon dioxide supplied from the outside
- a fuel gas supply device for controlling the concentration of the target component gas in the fuel gas of the gas engine within the setting range and supplying the gas gas as the fuel gas, carbon dioxide concentration and methane concentration of the mixed gas
- a gas concentration sensor that measures the concentration of at least one of When the target component gas is carbon dioxide, the fuel gas supply device has a concentration of the target component gas lower than the setting range, or when the target component gas is methane, the target component gas has a concentration of the target component gas
- a first gas supply device for supplying a first concentration adjusting gas mainly composed of methane to the mixed gas having a high concentration, and when the target component
- a second gas supply device If the target component gas is carbon dioxide and the concentration of the target component gas of the mixed gas is higher than the setting range, or the first gas supply device determines that the target component gas is carbon dioxide based on the measurement result of the gas concentration sensor When the component gas is methane and the concentration of the target component gas of the mixed gas is lower than the set range, the first concentration adjusting gas is supplied to the mixed gas, and methane and carbon dioxide in the mixed gas are supplied.
- the second gas supply device may be based on the measurement result of the gas concentration sensor, or the target When the component gas is methane and the concentration of the target component gas of the mixed gas is higher than the set range, the second concentration adjusting gas is supplied to the mixed gas to mix methane and carbon dioxide in the mixed gas.
- the ninth feature is to control the concentration.
- the concentration fluctuation Since any one of the first concentration adjusting gas and the second concentration adjusting gas can be supplied to the mixed gas to control the concentrations of methane and carbon dioxide in the mixed gas, the concentration of methane or carbon dioxide is Since the mixed gas controlled within the setting range according to the gas engine to be used is supplied to the gas engine as the fuel gas, even if the above concentration fluctuation of the mixed gas supplied from the outside is large, the load applied to the gas engine It can be greatly reduced and the service life of the gas engine can be extended.
- the mixed gas when the mixed gas is stably supplied at a certain carbon dioxide concentration and methane concentration and the carbon dioxide concentration of the mixed gas increases and the methane concentration decreases in a situation where the gas engine is operating stably.
- the first gas supply device can supply the first concentration adjusting gas to the mixed gas to suppress an increase in carbon dioxide concentration in the mixed gas and a decrease in methane concentration
- the above-described stable gas engine Can maintain the operation of
- the second gas supply device supplies a second concentration adjusting gas to the mixed gas to reduce the carbon dioxide concentration of the mixed gas, Since the increase in the methane concentration can be suppressed, the stable gas engine operation described above can be maintained as well.
- the fuel gas supply device selectively removes carbon dioxide contained in the mixed gas with respect to methane, and the carbon dioxide removal device It is preferable to provide a first container and a second container for separately storing the first concentration adjusting gas and the second concentration adjusting gas, which are prepared in advance by separating carbon dioxide from the mixed gas by using the first concentration adjusting gas and the second concentration adjusting gas.
- the carbon dioxide concentration of the mixed gas is reduced and the methane concentration is increased, so that the first concentration adjusting gas can be prepared, and the carbon dioxide removal device
- the second concentration adjusting gas can be prepared by recovering the carbon dioxide separated in step (d), and the first concentration adjusting gas and the second concentration adjusting gas prepared in advance are separately stored in the first container and the second container. It can be stored in a container and can be used for the utilization of the first gas supply device and the second gas supply device.
- the mixed gas contains a gas derived from biogas generated by methane fermentation of an organic substance. This makes it possible to realize a long-lived power generation system using biogas.
- the power generation system in a power generation system which generates a fuel gas containing carbon dioxide mainly containing methane to the engine to generate electricity, the fluctuation of the carbon dioxide concentration and the methane concentration of the fuel gas is suppressed and stabilized. Operation of the gas engine can be maintained, and a long-lived power generation system can be realized.
- FIG. 8 is a block diagram schematically showing another configuration example of the water vapor supply unit. Graph showing the CH 4 purity of the CO 2 recovery rate and the fuel gas CO 2 removal device, the simulation results of the relationship between the feed gas flow rate Ff.
- the graph which shows the result of having simulated the relationship between the CO 2 recovery rate of a CO 2 removal apparatus, CH 4 purity of fuel gas, and supply side pressure Pf.
- Graph showing the CH 4 purity of the CO 2 recovery rate and the fuel gas CO 2 removal device the simulation results of the relationship between the permeate side pressure Ps.
- Graph showing the CH 4 purity of the CO 2 recovery rate and the fuel gas CO 2 removal device the simulation results of the relationship between the sweep gas flow rate Fs.
- Graph showing the CH 4 purity of the CO 2 recovery rate and the fuel gas CO 2 removal device the simulation results of the relationship between the ambient temperature Ta.
- Graph showing the CH 4 purity of the CO 2 recovery rate and the fuel gas CO 2 removal device the simulation results of the relationship between the membrane area Sm.
- FIG. 10 is a list showing conditions used to obtain each simulation result shown in FIG. 5 to FIG.
- FIG. 5 is a block diagram schematically showing a configuration example of a fuel gas supply device and an operating condition control device according to a second embodiment.
- the block diagram which shows typically the structural example of the 1st gas supply apparatus which concerns on 2nd Embodiment.
- the block diagram which shows typically the structural example of the 2nd gas supply apparatus which concerns on 2nd Embodiment.
- the block diagram which shows typically the schematic structural example of the electric power generation system which concerns on 3rd Embodiment.
- FIG. 8 is a block diagram schematically showing a configuration example of a fuel gas supply device according to a third embodiment.
- the present system a power generation system (hereinafter, appropriately referred to as “the present system”) according to some embodiments of the present invention will be described with reference to the drawings.
- FIG. 1 is a block diagram schematically showing a schematic configuration example of the present system 10.
- the system 10 includes a gas engine 11, a generator 12, a fuel gas supply device 13, and a gas concentration sensor 14.
- a gas engine 11 and one generator 12 are provided.
- a plurality of gases are assumed.
- the engine 11 or a plurality of sets of the gas engine 11 and the generator 12 may be provided.
- the arrow in FIG. 1 simplifies and shows the flow path and direction through which gas flows.
- the description of the three-way valve, the mixing valve, etc. required in the gas flow path is omitted.
- the same reference numeral is given to the same component, and the description thereof may be omitted.
- the gas engine 11 mixes fuel gas FG containing carbon dioxide such as biogas or natural gas with carbon dioxide as a main component with air, burns it in the combustion chamber, and moves heat energy generated by the combustion reaction of the fuel gas FG. It is a biogas engine or natural gas engine that converts it into energy and outputs it. Operation control of the gas engine 11 (for example, control of supply amount and supply timing of fuel gas FG, ignition timing, throttle opening (air supply amount), valve timing (opening and closing timing of intake valve and exhaust valve), etc.)
- the engine control unit to perform is attached as a part of gas engine 11, and illustration is abbreviate
- the generator 12 is configured using an alternator such as a synchronous generator or an induction generator having a rotor and a stator, and converts kinetic energy supplied from the gas engine 11 into electric energy to convert AC power. Output.
- alternator such as a synchronous generator or an induction generator having a rotor and a stator
- the structure and type of alternator are not limited to any particular structure and type.
- the AC power output from the generator 12 is output to the inverter device 15 as necessary, and after the primary AC power output from the generator 12 is once converted to DC power in the inverter device 15, desired
- the secondary AC power is converted to a secondary AC power of the form (single-phase or three-phase), supplied to a predetermined power load, and is also grid-connected as required.
- the inverter device 15 is not necessarily a component of the system 10, but may be part of the system 10.
- the fuel gas supply device 13 controls the concentration of at least one target component gas of methane and carbon dioxide in the mixed gas MG with respect to the mixed gas MG having methane and carbon dioxide supplied from the outside as main components.
- the base is controlled to be within the setting range for the concentration (the dry base) of the target component gas in the fuel gas FG of the gas engine 11, and is supplied to the gas engine 11 as the fuel gas FG.
- mixed gas derived from biogas obtained by methane fermentation of organic waste such as biomass and sewage sludge is used as mixed gas MG.
- the mixed gas MG derived from biogas is an impurity such as hydrogen sulfide or siloxane, an impurity removing device (not shown) such as an existing desulfurization device or a siloxane removal device of activated carbon adsorption type. It is removed in advance before being supplied to the fuel gas supply device 13.
- an impurity removing device such as an existing desulfurization device or a siloxane removal device of activated carbon adsorption type. It is removed in advance before being supplied to the fuel gas supply device 13.
- the carbon dioxide concentration and the methane concentration of the mixed gas MG, the fuel gas FG, and the like are the concentrations on a dry basis.
- a wet desulfurization method using an absorbing solution or an adsorption desulfurization method using a sulfur adsorbent such as zinc oxide or iron oxide can be used.
- sulfur adsorbent such as zinc oxide or iron oxide
- sulfur adsorbent such as zinc oxide or iron oxide
- sulfur can be completely removed to the ppb level or less.
- the promoted transport film may be affected by hydrogen sulfide depending on the type of carrier used and the concentration thereof, so a superhigh-order desulfurization catalyst is used Is preferred.
- the mixed gas MG is directly supplied to the fuel gas supply device 13 from the biogas production facility through the pipeline and the above-mentioned impurity removing device or the like, or the biogas from the biogas production facility to the storage tank After temporarily storing, various supply modes such as a configuration to be supplied to the fuel gas supply device 13 through the pipeline and the above-mentioned impurity removal device can be used.
- the fuel gas supply device 13 controls the operating conditions that affect the increase and decrease of the carbon dioxide removal rate of the CO 2 removal device 16 that removes carbon dioxide in the mixed gas MG and the CO 2 removal device 16. 17 is provided.
- CO 2 removal device 16 various gas separation methods such as membrane separation, chemical absorption, pressure swing adsorption (PSA), temperature swing adsorption (TSA), etc. can be used.
- PSA pressure swing adsorption
- TSA temperature swing adsorption
- a CO 2 separation membrane 20 by a membrane separation method is provided.
- the CO 2 removing device 16 has a first processing chamber 21 and a second processing chamber 21 separated by a CO 2 separation membrane 20 and a CO 2 separation membrane 20.
- the processing chamber 22 is provided.
- the mixed gas controlled within the above setting range (the setting range Wch4 of methane concentration or the setting range Wco2 of carbon dioxide concentration) is discharged to the outside of the first processing chamber 21 as the fuel gas FG in a manner described later.
- a first outlet 21b is provided.
- FIG. 2A is a cross-sectional view of two types schematically showing the schematic structure of the CO 2 removing device 16 when the CO 2 separation membrane 20 is flat.
- the cross section of each cross-sectional view of FIG. 2A is orthogonal to the CO 2 separation film 20 and orthogonal to each other.
- FIG. 2B is a cross-sectional view of two types schematically showing the schematic structure of the CO 2 removing device 16 when the CO 2 separation membrane 20 has a cylindrical shape.
- the cross section of each cross-sectional view of FIG. 2A is a cross section passing through the axial center of the cylindrical CO 2 separation film 20 and a cross section orthogonal to the axial center. Therefore, the dimensional ratio of each part of FIG. 2 (A) and (B) does not necessarily correspond with the dimensional ratio of each part of the actual CO 2 removal apparatus 16. Arrows in FIGS. 2A and 2B schematically indicate the flowing direction of the gas in each part.
- the gas engine 11 is a biogas engine, for example, 65% ⁇ 5% or 70% ⁇ 5% is assumed as the setting range Wch4 of methane concentration, and when the gas engine 11 is a natural gas engine, for example, 80% ⁇ 5% or 85% ⁇ 5% etc. are assumed. Further, if the gas engine 11 is a biogas engine, for example, 35% ⁇ 5% or 30% ⁇ 5% is assumed as the setting range Wco2 of the carbon dioxide concentration, and if the gas engine 11 is a natural gas engine For example, 20% ⁇ 5% or 15% ⁇ 5% are assumed. However, when setting both the methane concentration setting range Wch4 and the carbon dioxide concentration setting range Wco2, if the methane concentration is within the setting range Wch4, the carbon dioxide concentration is also set within the setting range Wco2 There is a need to.
- a CO 2 -promoting transport membrane in which a known CO 2 carrier selectively reacting with carbon dioxide without reacting with methane is added to the gel membrane.
- CO 2 -facilitated transport membrane carbon dioxide is permeated as a reaction product with a CO 2 carrier in addition to physical permeation by a dissolution / diffusion mechanism, so that the permeation rate is promoted.
- gases such as methane, nitrogen and hydrogen which do not react with the CO 2 carrier permeate only by the dissolution / diffusion mechanism, the separation coefficient of carbon dioxide to these gases is extremely large.
- CO 2 carrier for example, cesium carbonate or bicarbonate, or carbonate or bicarbonate of an alkali metal such as rubidium carbonate or rubidium bicarbonate can be mentioned.
- hydroxides of alkali metals such as cesium hydroxide or rubidium hydroxide can also be said to be equivalent because they react with carbon dioxide to form carbonates and carbonates.
- amino acids such as 2,3-diaminopropionate (DAPA) and glycine are known to exhibit high CO 2 selective permeation performance.
- the CO 2 -facilitated transport film can be configured by supporting a gel layer, which is configured to include the above-mentioned CO 2 carrier in a gel film, on a hydrophilic or hydrophobic porous film.
- a gel layer which is configured to include the above-mentioned CO 2 carrier in a gel film, on a hydrophilic or hydrophobic porous film.
- the film material constituting the gel film include polyvinyl alcohol (PVA) film, polyacrylic acid (PAA) film, polyvinyl alcohol-polyacrylic acid (PVA / PAA) salt copolymer film, and the like.
- CO 2 -facilitated transport membrane of the structure are known to exhibit a high CO 2 selective permeability (e.g., Japanese Patent 4621295, JP 2008-036463, patent publications such as JP 2013-049048, published See patent publication).
- the CO 2 -facilitated transport membrane has a very low permeation rate of carbon dioxide when there is no moisture in the membrane, and the moisture in the membrane is essential for obtaining a high permeation rate.
- the gel membrane is preferably a hydrogel membrane.
- the gel membrane By configuring the gel membrane with a high water-retention hydrogel membrane, it is possible to retain water in the membrane as much as possible even in an environment in which water in the gel membrane decreases (for example, high temperature of 100 ° C. or higher). It is possible to realize high CO 2 permeance.
- the polyvinyl alcohol-polyacrylic acid (PVA / PAA) salt copolymer membrane and the polyacrylic acid membrane are hydrogel membranes.
- the hydrogel is a three-dimensional network structure formed by crosslinking a hydrophilic polymer by chemical crosslinking or physical crosslinking, and has a property of swelling by absorbing water.
- the CO 2 removing device 16 includes a steam supply unit 18 that supplies steam (water vapor) to both the mixed gas MG and the sweep gas SG.
- the steam supply unit 18 generates steam internally or receives supply of steam from the outside, and as shown in FIG. 3, a first supply pipe 23a connected to the first receiving port 21a, and a second receiving pipe 23a.
- the steam is separately supplied to the second supply pipe 24a connected to the inlet 22a.
- each relative humidity of mixed gas MG and sweep gas SG can be separately set to arbitrary predetermined values.
- the steam supply unit 18 When the steam supply unit 18 generates steam inside, the water may be heated by heat exchange with the high temperature exhaust gas discharged from the gas engine 11 to generate the steam. Thereby, the waste heat of the said exhaust gas can be used effectively.
- steam is added to the mixed gas MG from the steam supply unit 18, steam (water vapor) is also included in the fuel gas FG immediately after being discharged from the first discharge port 21b.
- the water vapor removing portion is connected to the first exhaust pipe 23b connected to the first discharge port 21b. 19 is installed.
- the water vapor removal unit 19 can use a known configuration that uses a water-vapor permeable membrane such as one using a condenser or a perfluoro-based membrane (or a perfluorosulfonic acid-based membrane).
- a water-vapor permeable membrane such as one using a condenser or a perfluoro-based membrane (or a perfluorosulfonic acid-based membrane).
- steam is recovered not in the cooled liquid state but in a gaseous state (with latent heat), so at least a portion of the removed steam is directly supplied to the water vapor supply portion It can be returned to 18 and reused as steam mixed with the mixed gas MG and the sweep gas SG (see FIG. 3). It is also possible to use the above-mentioned facilitated transport membrane as the water vapor permeable membrane.
- the facilitated transport membrane may be composed of a material different from that of the CO 2 separation membrane 20 or may be composed of the same material.
- An example of a water vapor permselective membrane using a facilitated transport membrane is disclosed in WO 2012/014900.
- a steam separation unit 18 a may be provided on the flow path of the exhaust gas XG discharged from the gas engine 11 to separate the water vapor contained in the exhaust gas XG.
- the separated steam is supplied to the steam supply unit 18 and can be added to the mixed gas MG and the sweep gas SG.
- the water vapor separation unit 18a can use a known configuration using a water vapor permeable membrane.
- a facilitated transport film can also be used for the water vapor separation unit 18a.
- various shapes such as a flat plate shape or a cylindrical shape (for example, a cylindrical shape) can be considered as the CO 2 -facilitated transport film.
- the CO 2 -promoting transport film is configured by forming a gel film containing a CO 2 carrier on the outer peripheral side surface or the inner peripheral side surface of the cylindrical porous support, the cylindrical CO 2 -promoting transport One of the first processing chamber 21 and the second processing chamber 22 is formed inside the membrane, and the other of the first processing chamber 21 and the second processing chamber 22 is formed outside the first processing chamber 21 or the second processing chamber 22.
- a plurality of CO 2 promoting transport films are provided in one housing, and a plurality of at least one of the first processing chamber 21 and the second processing chamber 22 are formed to make the plurality of first processing chambers 21 communicate with each other, or The plurality of second processing chambers 22 may be communicated with each other, or both of them may be performed to increase the membrane area.
- the operating condition control device 17 is an operating condition that affects the increase or decrease in the carbon dioxide removal rate of the CO 2 removal device 16, that is, the carbon dioxide removal rate of the CO 2 separation membrane (CO 2 -fa
- the flow rate of the mixed gas MG supplied into the first processing chamber 21 supply gas flow rate Ff
- the pressure in the first processing chamber 21 supply side pressure Pf
- the second processing chamber 22 the pressure of the inner (permeate side pressure Ps)
- membrane area of ambient temperature Ta CO 2 separation membrane 20 of the second flow rate of sweep gas SG to be supplied into the processing chamber 22
- weep gas flow rate Fs CO 2 separation membrane 20
- At least one of the control target operation condition candidates including Sm is controlled based on the measurement result of the gas concentration sensor 14 described later.
- the operating condition control device 17 increases or decreases the carbon dioxide removal rate of the CO 2 removing device 16 by controlling at least one of the operating conditions included in the control target operating condition candidate, and as a result, the fuel gas Control is performed to maintain the methane concentration or carbon dioxide concentration of FG within the setting range Wch4 or the setting range Wco2.
- the gas concentration sensor 14 is, as shown in FIGS. 1 and 3, the first supply pipe 23a connected to the first inlet 21a, that is, the methane concentration of the mixed gas MG installed at the front stage of the CO 2 removing device 16 It is a gas sensor that measures the concentration of at least one of (dry basis) and carbon dioxide concentration (dry basis).
- the mixed gas MG is derived from biogas, so on a dry basis, the methane concentration fluctuates in the range of about 50% to 75% above the explosive upper limit concentration (15 vol%), and the carbon dioxide concentration May vary in the range of about 25% to 50%, so the gas concentration sensor 14 measures high concentration that covers the above variation range, regardless of whether the target component gas is methane or carbon dioxide.
- the mixed gas MG is derived from biogas, so on a dry basis, the methane concentration fluctuates in the range of about 50% to 75% above the explosive upper limit concentration (15 vol%), and the carbon dioxide concentration May vary in the range of about 25% to 50%, so the gas concentration sensor 14 measures high concentration that covers the
- the gas concentration sensor 14 may be disposed downstream of the CO 2 removal device 16.
- the methane concentration of the mixed gas (fuel gas FG) after passing through the CO 2 removing device 16 is controlled within the setting range Wch4, and the carbon dioxide concentration is controlled within the setting range Wco2.
- the concentration sensor 14 uses a well-known gas sensor capable of high concentration measurement which covers the above-mentioned set range, regardless of whether the target component gas is methane or carbon dioxide. Even if the target component gas is either methane or carbon dioxide, in the mixed gas MG derived from biogas, the concentration fluctuation of methane and carbon dioxide mainly occurs, and when one increases, the other decreases accordingly.
- the gas concentration sensor 14 may measure only one of the methane concentration and the carbon dioxide concentration and derive the other from the one measurement result. In the following description, including the case of deriving the other from the measurement result of one of the methane concentration and the carbon dioxide concentration, it is collectively referred to as “measurement etc.”.
- the operating condition control device 17 sets the flow rate of the mixed gas MG to the first supply pipe 23a connected to the first receiving port 21a.
- the back pressure valve 26 is interposed in the first exhaust pipe 23 b connected to the first discharge port 21 b, and the back pressure valve 26 is installed.
- the pressure gauge 27 is provided on the upstream side of the mass flow controller, which controls the flow rate of the sweep gas SG to the second supply pipe 24a connected to the second receiving port 22a when using the sweep gas flow rate Fs as the above operation condition
- the back pressure valve 29 is interposed in the second exhaust pipe 24b connected to the second discharge port 22b, and the upstream side of the back pressure valve 29 is used.
- the pressure gauge 30 is provided to further mass flow controller 25 and 28, a control unit 17a for controlling the back pressure valve 26 and 29 or the like, and controllable constituting the respective operating conditions.
- the mass flow controllers 25 and 28 also function as mass flow meters, control states of the supply gas flow rate Ff and the sweep gas flow rate Fs by the mass flow controllers 25 and 28 can be confirmed by themselves.
- the pressure gauge 27 is for confirming the control state of the supply side pressure Pf by the back pressure valve 26, and the pressure gauge 30 is for confirming the control state of the permeation side pressure Ps by the back pressure valve 29. . Therefore, the mass flow controller 25, the back pressure valve 26, and the pressure gauge 27 are used depending on which operation condition of the supply gas flow rate Ff, supply side pressure Pf, sweep gas flow rate Fs, and permeation side pressure Ps is used as a control target.
- the control unit 17a is a control device capable of processing digital signals or analog signals and the like configured to include a microcomputer, programmable logic, and the like.
- the operating condition controller 17 When the ambient temperature Ta of the CO 2 separation membrane 20 is used as the above-mentioned operating condition, the operating condition controller 17 further installs the operating condition controller 17 in, for example, a constant temperature bath, and CO as the above-mentioned operating condition. 2
- the CO 2 separation membrane 20 is divided into a plurality of membrane units, and the first processing chamber 21 and the second processing chamber 22 are provided in each of the membrane units to mix them.
- the number of film units supplying the gas MG can be increased or decreased, and the operating conditions of the ambient temperature Ta and the film area Sm can be controlled from the control unit 17a.
- FIGS. 5 to 10 simulation results showing that each of the above operating conditions can actually control the increase and decrease of the carbon dioxide removal rate are shown in FIGS. 5 to 10 according to the operating conditions.
- 5 shows the case where the operating condition is the supplied gas flow rate Ff
- FIG. 6 shows the case where the operating condition is the supply side pressure Pf
- FIG. 7 shows the case where the operating condition is the permeation side pressure Ps
- FIG. 9 shows the simulation results when the operation condition is the ambient temperature Ta
- FIG. 10 shows the simulation results when the operation condition is the film area Sm.
- the vertical axes in FIG. 5 to FIG. 10 indicate the CO 2 recovery rate [%] of the CO 2 removal device 16 and the CH 4 purity [%] of the fuel gas FG, and the horizontal axes indicate the respective operating conditions.
- the CO 2 recovery rate [%] is calculated as a value (percentage) obtained by dividing the flow rate of carbon dioxide in the mixed gas EG discharged from the second outlet 22 b by the flow rate of carbon dioxide in the mixed gas MG, It represents the carbon removal rate.
- the CH 4 purity [%] is calculated as a value (percentage) obtained by dividing the flow rate of methane in the fuel gas FG discharged from the first outlet 21 b by the flow rate (dry base) of the fuel gas FG.
- FIG. 11 The conditions used for each simulation are summarized in FIG. In FIG. 11, the value of the item which is the operating condition is displayed as "variable".
- the composition ratio (volume ratio) of the mixed gas MG is shown on a dry basis, but steam (steam) is maintained so that the relative humidity is maintained at 70% under the temperature condition and pressure condition shown in FIG. ) Is added.
- the composition ratio (volume ratio: wet base) of the sweep gas SG is set such that the relative humidity is maintained at 70% under the same temperature and pressure conditions. Therefore, in FIG. 7, the composition ratio of the sweep gas SG is omitted according to the transmission side pressure Ps when the relative humidity is fixed at 70%, and therefore the display is omitted.
- the relative humidity of the mixed gas MG and sweep gas SG is fixed to 70%, by eliminating the influence of the variation of the relative humidity, CO 2 of each operating condition is CO 2 remover 16 This is to make it possible to evaluate only the recovery rate [%] and the influence of the fuel gas FG on CH 4 purity [%].
- the controller 17a supplies the mass flow controller 25.
- the controller 17a supplies the mass flow controller 25.
- the controller 17a supplies the back pressure valve 26 By performing control to increase the side pressure Pf to increase the CO 2 recovery rate, it is possible to maintain the methane concentration of the fuel gas FG in the setting range Wch4 or the carbon dioxide concentration in the setting range Wco2.
- the controller 17a supplies the back pressure valve 26 By performing control to lower the side pressure Pf to lower the CO 2 recovery rate, it is possible to maintain the methane concentration of the fuel gas FG within the setting range Wch4 or the carbon dioxide concentration within the setting range Wco2.
- control unit 17a permeates the back pressure valve 29.
- the control unit 17a permeates the back pressure valve 29.
- control unit 17a sweeps the mass flow controller 28. By performing control to lower the gas flow rate Fs and lowering the CO 2 recovery rate, it is possible to maintain the methane concentration of the fuel gas FG in the above setting range Wch4 or the carbon dioxide concentration in the above setting range Wco2.
- control unit 17a controls the ambient temperature with respect to the thermostatic bath It is possible to maintain the methane concentration of the fuel gas FG in the set range Wch4 or the carbon dioxide concentration in the set range Wco2 by performing control to reduce Ta and reducing the CO 2 recovery rate.
- the control unit 17a sends the CO 2 removing device 16 Control to increase the number of membrane units (membrane area Sm) to be used to increase the CO 2 recovery rate, the methane concentration of the fuel gas FG is in the above setting range Wch 4 or the carbon dioxide concentration is in the above setting range Can be maintained at Wco2.
- the control unit 17a sends a signal to the CO 2 removal device 16 Control to reduce the number of membrane units (membrane area Sm) to be used to reduce the CO 2 recovery rate, the methane concentration of the fuel gas FG is in the above setting range Wch 4 or the carbon dioxide concentration is in the above setting range Can be maintained at Wco2.
- any operating condition of supply gas flow rate Ff, supply side pressure Pf, permeation side pressure Ps, sweep gas flow rate Fs, ambient temperature Ta, and film area Sm is used because positive or negative correlation exists between each operating condition and CO 2 recovery rate [%] and CH 4 purity [%], it is possible to control increase or decrease in carbon dioxide removal rate I understand.
- the relative humidity of the mixed gas MG and the sweep gas SG is fixed at a constant value in each of the above simulations.
- the relative humidity of the mixed gas MG and the sweep gas SG does not necessarily have to be fixed at a constant value, and each relative humidity is set at a constant value in the first processing chamber 21 and the second processing chamber 22. It is difficult to maintain. For example, when the pressure (supply side pressure Pf or permeation side pressure Ps) in the first processing chamber 21 or the second processing chamber 22 is increased, the water vapor partial pressure in the first processing chamber 21 or the second processing chamber 22 is increased.
- the relative humidity in the first processing chamber 21 or the second processing chamber 22 rises and the ambient temperature Ta of the CO 2 separation film 20 rises, the saturated vapor pressure in the first processing chamber 21 or the second processing chamber 22 As it increases, the relative humidity in the first process chamber 21 or the second process chamber 22 decreases. As the relative humidity in the first processing chamber 21 and the second processing chamber 22 is higher, the facilitated transport function of the CO 2 facilitated transport film is exhibited, the CO 2 permeance is increased, and the CO 2 recovery rate is increased.
- the relative humidity in the first processing chamber 21 and in the second processing chamber 22 corresponds to the pressure in the first processing chamber 21 or the second processing chamber 22 (supply side pressure Pf or permeation side pressure Ps) and the CO 2 separation membrane 20.
- supply side pressure Pf or permeation side pressure Ps supply side pressure
- CO 2 separation membrane 20 CO 2 separation membrane 20.
- the ambient temperature Ta it changes according to the amount of steam (steam) added to the mixed gas MG and the sweep gas SG.
- the amount of added water vapor to the mixed gas MG and the sweep gas SG is also the operating condition used by the operating condition control device 17, the supply gas flow rate Ff, supply side pressure Pf, permeation side
- the pressure Ps, the sweep gas flow rate Fs, the ambient temperature Ta, and the film area Sm can be added to the above-mentioned operating condition candidate for control target, and the operating condition control device 17 And at least one of the above operating conditions may be used.
- the CO 2 recovery rate [%] and the CH 4 purity [%] have a negative correlation with the permeation side pressure Ps, but on the other hand, they are supplied into the second processing chamber 22
- the composition ratio (partial pressure ratio) of water vapor in the sweep gas SG to be measured is constant
- the relative humidity in the second processing chamber 22 increases (or decreases) as the permeation pressure Ps increases (or decreases).
- the CO 2 recovery rate [%] and the CH 4 purity [%] have a positive correlation that increases (or decreases). That is, the effect of the increase and decrease of the permeation pressure Ps is suppressed by the change of the relative humidity in the second processing chamber 22.
- the water vapor supply unit 18 is adjusted according to the change of the permeation side pressure Ps so that the relative humidity of the sweep gas SG is maintained constant as in the simulation. It is preferable to perform control to change the water vapor partial pressure of the sweep gas SG by adjusting the amount of water vapor supplied from the above.
- the CO 2 recovery rate [%] and the CH 4 purity [%] have a positive correlation with the supply side pressure Pf, while the first processing chamber 21
- the composition ratio (partial pressure ratio) of steam in the mixed gas MG supplied to the inside is constant, the relative humidity in the first processing chamber 21 increases (or decreases) when the supply pressure Pf increases (or decreases).
- the CO 2 recovery rate [%] and the CH 4 purity [%] have a positive correlation that increases (or decreases). That is, the effect of the increase or decrease of the supply side pressure Pf is enhanced by the change of the relative humidity in the first processing chamber 21. Therefore, when the supply side pressure Pf is used as the operation condition, it is not necessary to control the water vapor partial pressure of the mixed gas MG so that the relative humidity of the mixed gas MG is maintained constant.
- the CO 2 recovery rate [%] and the CH 4 purity [%] have a positive correlation with the ambient temperature Ta, while on the other hand, in the first processing chamber 21.
- the composition ratio (partial pressure ratio) of water vapor in the supplied mixed gas MG and the composition ratio (partial pressure ratio) of water vapor in the sweep gas SG supplied into the second processing chamber 22 is constant,
- the temperature Ta rises (or falls) the saturated water vapor pressure rises (or falls), so the relative humidity in at least one of the first processing chamber 21 and the second processing chamber 22 falls (or increases), CO 2 recovery [%] and CH 4 purity [%] have a negative correlation with decreasing (or increasing).
- the effect due to the increase or decrease of the ambient temperature Ta is suppressed by the change in the relative humidity of at least one of the inside of the first processing chamber 21 and the inside of the second processing chamber 22. Therefore, when the ambient temperature Ta is used as the above operating condition, as in the simulation, the water vapor is adjusted according to the change of the ambient temperature Ta so that the relative humidity of the mixed gas MG and the sweep gas SG is maintained constant. It is preferable to perform control to adjust the amount of water vapor supplied from the supply unit 18 and change the water vapor partial pressures of the mixed gas MG and the sweep gas SG.
- the relationship between at least one of the concentration and the carbon dioxide concentration, and the concentration of the target component gas (methane or carbon dioxide) in the fuel gas FG whose concentration is controlled by the CO 2 removal device 16 is obtained by experiments in advance. Get it.
- the operating condition control device 17 controls the fuel based on at least one of the methane concentration and the carbon dioxide concentration measured by the gas concentration sensor 14 during operation of the system 10.
- the above operating conditions necessary to maintain the concentration of the target component gas (methane or carbon dioxide) in the gas FG within the above setting range (methane concentration setting range Wch4 or carbon dioxide concentration setting range Wco2)
- the value of is controlled to a value derived from the relationship previously obtained by experiments or the like.
- the operating condition control device 17 measures the gas concentration sensor 14 that measures the concentration of the target component gas (methane or carbon dioxide) in the fuel gas FG.
- the concentration of the target component gas in the fuel gas FG is in the above-mentioned setting range (methane concentration based on the measurement result of the gas concentration sensor 14 by adding or moving downstream of the back pressure valve 26 of the first exhaust pipe 23b. It is good also as composition of performing control of a feedback type which carries out increase and decrease of the value of the above-mentioned operating conditions so that it may be maintained in setting range Wch4 of this, or setting range Wco2 of a carbon dioxide concentration.
- the operating condition control device 17 normally uses the number of the operating conditions to be used. It is also preferable to increase or decrease the carbon dioxide removal rate of the CO 2 removal device 16 more quickly by increasing the number.
- the fuel gas FG supplied from the first processing chamber 21 toward the gas engine 11 is The flow rate or pressure changes in accordance with the change of the supply gas flow rate Ff or the supply side pressure Pf. Therefore, as shown in FIG. 3, in the case where the supply gas flow rate Ff is used as the above-mentioned operation condition, mass flow for adjusting the flow rate to the predetermined value to the first supply pipe 23a in order to suppress the flow rate fluctuation of the fuel gas FG.
- a pressure adjusting device 32 such as a pressure adjusting valve for adjusting the pressure to a predetermined value is interposed.
- the schematic configuration of the present system 10a according to the second embodiment is basically the same as the present system 10 according to the first embodiment.
- the system 10a and the system 10 includes a fuel gas supply apparatus 13a of the system 10a is, as shown in FIG. 12, includes a first gas supply unit 40 and a second gas supply unit 50, the CO 2 remover 16 In the first exhaust pipe 23b connected to the first exhaust port 21b, however, the first gas supply device 40 performs the first concentration adjustment downstream of the first exhaust pipe 23b when the back pressure valve 26 is interposed.
- the difference is that a configuration is provided in which the gas BG1 is supplied and the second gas supply device 50 supplies the second concentration adjustment gas BG2.
- the parts common to the fuel gas supply apparatus 13 other than the added first gas supply apparatus 40 and the second gas supply apparatus 50 are the same as in the first embodiment, and therefore, the fuel gas supply apparatus 13a is the same as the first embodiment. I will omit it.
- the gas engine 11, the generator 12, and the gas concentration sensor 14 are the same as those in the first embodiment, duplicate descriptions will be omitted.
- the first gas supply device 40 makes the carbon dioxide concentration lower than the setting range Wco2 of the carbon dioxide concentration according to whether the target component gas is methane or carbon dioxide
- the first concentration adjusting gas BG1 generated in advance so that the methane concentration is higher than the setting range Wch4 of the methane concentration or both of them may be stored in the first container 45, and the control unit
- the first concentration adjusting gas BG1 in the first container 45 is configured to be supplied to the first exhaust pipe 23b in accordance with an instruction from 17a.
- the control unit 17a causes the first gas supply device 40 to generate the carbon dioxide concentration.
- the control unit 17 a calculates.
- the first gas supply device 40 includes a CO 2 separation device 41 that generates the first concentration adjustment gas BG1 in advance.
- CO 2 separation device 41 the same configuration as CO 2 removal unit 16, a CO 2 separation membrane 42 of the CO 2 -facilitated transport membrane, the first processing chamber 43 and the second processing chamber separated by the CO 2 separation membrane 42 It comprises 44.
- the mixed gas MG derived from the same biogas as the mixed gas MG supplied to the first processing chamber 21 of the CO 2 removing device 16 is any of the various supply modes described in the first embodiment. It is supplied using The mixed gas MG supplied to the first processing chamber 43 has a carbon dioxide concentration by selectively permeating carbon dioxide to the second processing chamber 44 side via the CO 2 separation membrane 42 of the CO 2 facilitated transport film.
- the mixed gas MG1 that has dropped significantly is discharged from the first processing chamber 43, and is stored in the first container 45 as a first concentration adjustment gas BG1.
- the sweep gas SG1 is supplied to the second processing chamber 44 in the same manner as the CO 2 removal device 16, and a mixed gas of a part of the mixed gas MG permeated from the first processing chamber 43 to the second processing chamber 44 and the sweep gas SG1.
- SG1 ' is discharged from the second processing chamber 44.
- the CO 2 / CH 4 selection ratio of the facilitated transport film used for the CO 2 separation membrane 42 is, for example, 100 or more, adjusting the operating conditions of the CO 2 separation device 42 results in an extremely high carbon dioxide removal rate. realizable. Therefore, by setting the carbon dioxide removal rate high according to the setting range Wch4 and the setting range Wco2, the mixed gas MG1 discharged from the first processing chamber 43 has a predetermined value (for example, a carbon dioxide concentration) in the setting range Wco2. It is possible to lower the concentration by 5 to 10 vol% or more or to increase the methane concentration by a predetermined value (for example, 5 to 10 vol%) or more than the set range Wch4.
- a predetermined value for example, 5 to 10 vol%
- the carbon dioxide concentration and the methane concentration of the mixed gas MG 1 change with the concentration fluctuation of carbon dioxide and methane in the mixed gas MG supplied to the first processing chamber 43, but the first stored in the first container 45
- the condition that the carbon dioxide concentration and the methane concentration of the concentration adjustment gas BG1 are lower than the set range Wco2 by the predetermined value or more and higher than the set range Wch4 by the predetermined value or more is satisfied.
- the first container 45 is provided with a gas concentration sensor 46 similar to the gas concentration sensor 14, and the measured values of carbon dioxide concentration and methane concentration of the first concentration adjusting gas BG1 Is notified to the control unit 17a. Then, the control unit 17a calculates the necessary flow rate taking into consideration the measurement result of the gas concentration sensor 46.
- the second gas supply device 50 makes the carbon dioxide concentration higher than the setting range Wco2 of the carbon dioxide concentration depending on whether the target component gas is methane or carbon dioxide
- the second concentration adjusting gas BG2 generated in advance so that the methane concentration is lower than the setting range Wch4 of the methane concentration or both of them may be stored in the second container 56, and the control unit
- the second concentration adjusting gas BG2 in the second container 56 is configured to be supplied to the first exhaust pipe 23b in accordance with an instruction from 17a.
- the controller 17 a causes the second gas supply device 50 to generate the carbon dioxide concentration.
- the control unit 17 a calculates.
- the second gas supply device 50 includes a CO 2 separation device 51 and a water vapor removal unit 55 that generate the second concentration adjustment gas BG 2 in advance.
- the water vapor removal unit 55 can use the same configuration as that of the water vapor removal unit 19 described in the first embodiment, and therefore redundant description will be omitted.
- the CO 2 separation device 51 has the same configuration as the CO 2 removal device 16 and includes a CO 2 separation film 52 of a CO 2 -facilitated transport film, and a first treatment chamber 53 and a second treatment chamber separated by the CO 2 separation film 52. It comprises 54.
- the first processing chamber 53 is supplied with the mixed gas EG having an increased carbon dioxide concentration, which is discharged from the second processing chamber 22 of the CO 2 removing device 16.
- the mixed gas EG supplied to the first processing chamber 53 is the sweep gas SG supplied to the second processing chamber 22 of the CO 2 removal device 16 and the mixed gas MG transmitted from the first processing chamber 21 to the second processing chamber 22.
- the component gas of the sweep gas SG for example, an inert gas such as argon
- the gas is selectively permeated to the second processing chamber 54 side and separated, and is discharged from the second processing chamber 54 as the mixed gas SG2 ′ together with the sweep gas SG2 supplied to the second processing chamber 53. Since the mixed gas SG2 ′ discharged from the second processing chamber 54 contains carbon dioxide and water vapor, it is stored in the second container 56 as the second concentration adjustment gas BG2 after the water vapor removal unit 55 removes the water vapor. .
- the inert gas or the like is mixed in the second concentration adjusting gas BG2
- the pressure in the second processing chamber 54 it is necessary to control the pressure in the second processing chamber 54 to be equal to or less than the saturated water vapor pressure at the temperature in the second processing chamber 54.
- the steam of the sweep gas SG2 can be supplied from the water vapor supply unit 18. Further, the water vapor removed by the water vapor removal unit 55 can be supplied to the water vapor supply unit 18 for reuse.
- the methane concentration of the mixed gas EG is extremely low, and further, the mixed gas with a low methane concentration The amount of methane in EG passing through the CO 2 separation membrane 52 is extremely small. Therefore, by setting the carbon dioxide removal rate of the CO 2 removal device 51 high according to the setting range Wch4 and the setting range Wco2, the methane concentration of the mixed gas SG2 ′ is set to a predetermined value (for example, 5 to 10 vol.) From the setting range Wch4.
- the carbon dioxide concentration of the mixed gas SG2 ′ can be set higher than the set range Wco2 by a predetermined value (eg, 5 to 10 vol%) or more.
- a predetermined value eg, 5 to 10 vol% or more.
- the condition that the carbon dioxide concentration and the methane concentration of the second concentration adjusting gas BG2 stored in the second container 56 are higher than the set range Wco2 by the predetermined value or more and lower than the set range Wch4 by the predetermined value or more is satisfied.
- the second container 56 is provided with a gas concentration sensor 57 similar to the gas concentration sensor 14, and the carbon dioxide concentration and the methane concentration of the second concentration adjusting gas BG2 are The measured value is configured to be notified to the control unit 17a. Then, the control unit 17a calculates the necessary flow rate taking into consideration the measurement result of the gas concentration sensor 46.
- the first gas supply device 40 supplies the first concentration adjustment gas BG1 downstream of the back pressure valve 26 and upstream of the water vapor removal unit 19 to supply the second gas.
- the device 50 supplies the second concentration adjusting gas BG2
- the supply of the first concentration adjusting gas BG1 and the second concentration adjusting gas BG2 is performed downstream of the water vapor removal unit 19 as shown in FIG. It is also preferred to do.
- the first gas supply device 40 has a water vapor removal unit 47 interposed between the first processing chamber 43 and the first container 45, and the mixed gas discharged from the first processing chamber 43. It is also preferable that the water vapor removal unit 47 remove water vapor contained in the MG1.
- the first gas supply device 40 includes the CO 2 separation device 41 and generates the first concentration adjusting gas BG1 in advance
- the first concentration adjusting gas BG1 is not provided.
- high purity methane gas such as natural gas supplied from the outside may be used.
- the second gas supply device 50 includes the CO 2 separation device 51, and uses the mixed gas EG in which the carbon dioxide concentration increased and discharged from the second processing chamber 22 of the CO 2 removal device 16 is used.
- the configuration for generating the second concentration adjusting gas BG2 in advance has been described, but instead of or in addition to the mixed gas EG, the exhaust gas containing carbon dioxide exhausted from the gas engine is transmitted to the first processing chamber 53 of the CO 2 separation device 51 May be supplied to the
- the present system 10 b is configured to include a gas engine 11, a generator 12, a fuel gas supply device 60, and a gas concentration sensor 14.
- the present system 10b includes a fuel gas supply device 60 in place of the fuel gas supply devices 13 and 13a of the present systems 10 and 10a in comparison with the present systems 10 and 10a of the first and second embodiments. It is different.
- the gas engine 11, the generator 12, and the gas concentration sensor 14 of the present system 10b are the same as those of the first embodiment, and thus redundant description will be omitted.
- the fuel gas supply device 60 includes a control unit 61, a first gas supply device 62, a second gas supply device 63, and a gas mixing unit 64.
- the control unit 61 is configured to include a microcomputer, a programmable logic, and the like, similarly to the control unit 17a of the first and second embodiments.
- the first gas supply device 62 supplies the first concentration adjusting gas BG1 generated in advance to the gas mixing unit 64 in accordance with an instruction from the control unit 61.
- the second gas supply device 63 supplies the second concentration adjusting gas BG2 generated in advance to the gas mixing unit 64 in accordance with an instruction from the control unit 61.
- the gas mixing unit 64 is configured of, for example, a four-way valve having three inlets and one outlet, and the mixed gas MG, the first concentration adjusting gas BG1, and the second concentration adjusting gas BG2 are respectively provided from the three inlets.
- a mixed gas which is separately supplied and in which one of the first concentration adjusting gas BG1 and the second concentration adjusting gas BG2 is added to the mixed gas MG in the gas mixing section 64 is used as the fuel gas FG in the gas engine 11 Supplied.
- the first concentration adjusting gas BG1 like the first concentration adjusting gas BG1 described in the second embodiment, has a carbon dioxide concentration corresponding to the above carbon dioxide concentration depending on whether the target component gas is methane or carbon dioxide It is prepared so as to be lower than the setting range Wco2 of the above, or so that the methane concentration becomes higher than the setting range Wch4 of the above-mentioned methane concentration, or both of them.
- the second concentration adjusting gas BG2 has a carbon dioxide concentration corresponding to the above carbon dioxide concentration depending on whether the target component gas is methane or carbon dioxide. It is prepared to be higher than the setting range Wco2 of the above, or so that the methane concentration is lower than the setting range Wch4 of the above-mentioned methane concentration, or both.
- the control unit 61 controls the first concentration adjusting gas BG1 and the first concentration adjusting gas BG1 with respect to one of the first gas supply device 62 and the second gas supply device 63 according to the carbon dioxide concentration or the methane concentration measured by the gas concentration sensor 14 or the like. It is instructed to supply one of the two concentration adjusting gas BG2 to the gas mixing unit 64 at a predetermined flow rate. Specifically, when the carbon dioxide concentration or the methane concentration measured by the gas concentration sensor 14 is higher than the set range Wco2 or lower than the set range Wch 4, the control unit 61 sends the first gas supply device 62.
- the first concentration adjusting gas BG1 is instructed to be supplied to the gas mixing unit 64 at a flow rate required for the carbon dioxide concentration or the methane concentration to fall within the set range Wco2 or within the set range Wch4.
- the necessary flow rate is a flow rate necessary for the carbon dioxide concentration or the methane concentration of the mixed gas obtained by adding the first concentration adjusting gas BG1 to the mixed gas MG to be within the set range Wco2 or within the set range Wch4.
- the control unit 61 calculates in consideration of the measurement result of the gas concentration sensor 14 and the supply flow rate of the mixed gas MG and the like.
- the control unit 61 sets the second gas supply device 63 to carbon dioxide It is instructed to supply the second concentration adjusting gas BG2 to the gas mixing unit 64 at a flow rate required for the carbon concentration or the methane concentration to fall within the set range Wco2 or within the set range Wch4.
- the necessary flow rate is a flow rate necessary for the carbon dioxide concentration or the methane concentration of the mixed gas obtained by adding the second concentration adjustment gas BG2 to the mixed gas MG to be within the set range Wco2 or within the set range Wch4.
- the control unit 61 calculates in consideration of the measurement result of the gas concentration sensor 14 and the supply flow rate of the mixed gas MG and the like. For this reason, in the present embodiment, a flow meter 65 such as a mass flow meter that measures the supply flow rate of the mixed gas MG is provided.
- the fuel gas supply device 60 uses the mixed gas MG derived from the same biogas as the mixed gas MG supplied to the gas mixing unit 64 to use the first concentration adjusted gas BG1 and the second concentration adjusted gas BG2 in advance.
- the structure which is produced and stored in the 1st container 70 and the 2nd container 73 is demonstrated with reference to FIG.
- the fuel gas supply device 60 includes a CO 2 separation device 66, a first container 70, a second container 73, and a water vapor removal unit 72 as the first gas supply device 62 and the second gas supply device 63.
- the first gas supply device 62 is composed of the CO 2 separation device 66 and the first container 70
- the second gas supply device 63 is composed of the CO 2 separation device 66, the second container 73 and the water vapor removal unit 72
- the second separation device 66 is commonly used by the first gas supply device 62 and the second gas supply device 63.
- the CO 2 separation device 66 has the same configuration as the CO 2 removal device 16 described in the first embodiment, and the first treatment separated from the CO 2 separation film 67 of the CO 2 facilitated transport film by the CO 2 separation film 67
- a chamber 68 and a second processing chamber 69 are provided.
- the first processing chamber 68 is supplied with the mixed gas MG derived from the same biogas as the mixed gas MG supplied to the gas mixing unit 64 using any of the various supply modes described in the first embodiment.
- Ru. Steam (water vapor) is supplied as sweep gas SG3 to the second processing chamber 69, and part of the mixed gas MG transmitted from the first processing chamber 68 to the second processing chamber 69 and mixed gas SG3 'of the sweep gas SG3 , And is discharged from the second processing chamber 69.
- the pressure in the second processing chamber 69 is controlled so that the temperature in the second processing chamber 69 becomes less than or equal to the saturated water vapor pressure, since steam (water vapor) is used as the sweep gas SG3.
- the steam of the sweep gas SG3 can be supplied from the water vapor supply unit by providing the water vapor supply unit in the same manner as the water vapor supply unit 18 of the first embodiment.
- the water vapor removed by the water vapor removal unit 72 can be supplied to the water vapor supply unit and reused.
- the mixed gas MG supplied to the first treatment chamber 68 has a carbon dioxide concentration by selectively permeating carbon dioxide to the second treatment chamber 69 side via the CO 2 separation film 67 of the CO 2 facilitated transport film.
- the greatly lowered mixed gas MG ′ is discharged from the first processing chamber 68 and stored in the first container 70 as a first concentration adjusting gas BG1.
- the sweep gas SG3 (steam) supplied to the second processing chamber 69 and a part (mainly carbon dioxide and water vapor, and a trace amount of methane) of the mixed gas MG permeated from the first processing chamber 68 side 2 is mixed in the processing chamber 69 and discharged from the second processing chamber 54 as a mixed gas SG3 ′ having a very high carbon dioxide concentration, and after the water vapor is removed by the water vapor removal unit 72, the second concentration adjusting gas BG2 is used as a second It is stored in the container 73.
- CO 2 / CH 4 selectivity of facilitated transport membrane used in the CO 2 separation device 66 for example, because it is more than 100, by adjusting the operating conditions of the CO 2 separation device 66, a very high carbon dioxide removal rate realizable. Therefore, by setting the carbon dioxide removal rate high according to the setting range Wch4 and the setting range Wco2, the carbon dioxide concentration of the mixed gas MG 'is set to a predetermined value (for example, 5 to 10 vol%) or more from the setting range Wco2.
- the methane concentration can be made lower than the set range Wch4 by a predetermined value (for example, 5 to 10 vol%) or more, and the methane concentration of the mixed gas SG3 ′ can be set to a predetermined value (for example, The carbon dioxide concentration can be lowered by 5 to 10 vol% or more or higher by a predetermined value (for example, 5 to 10 vol%) than the set range Wco2.
- the carbon dioxide concentration and the methane concentration of the mixed gas MG 'and the mixed gas SG3' change with the concentration fluctuation of carbon dioxide and methane in the mixed gas MG supplied to the first processing chamber 68. Therefore, the condition that the carbon dioxide concentration and the methane concentration of the first concentration adjustment gas BG1 stored in the first container 70 are lower than the set range Wco2 by the predetermined value or more and higher than the set range Wch4 by the predetermined value or more is satisfied.
- the first container 70 is provided with a gas concentration sensor 71 similar to the gas concentration sensor 14, and the carbon dioxide concentration and the methane concentration of the first concentration adjusting gas BG1 are The measurement value of the is transmitted to the control unit 61.
- the control unit 61 calculates the necessary flow rate of the first concentration adjusting gas BG1 taking into consideration the measurement result of the gas concentration sensor 71 as well. Similarly, the condition that the carbon dioxide concentration and the methane concentration of the second concentration adjusting gas BG2 stored in the second container 73 are higher than the set range Wco2 by the predetermined value or more and lower than the set range Wch4 by the predetermined value or more is satisfied. Although the actual concentration is unknown, the second container 73 is provided with a gas concentration sensor 74 similar to the gas concentration sensor 14, and the carbon dioxide concentration and the methane concentration of the second concentration adjusting gas BG2 are The measurement value of the is transmitted to the control unit 61. Then, the control unit 61 calculates the above-mentioned necessary flow rate of the second concentration adjusting gas BG2 in consideration of the measurement result of the gas concentration sensor 74.
- the CO 2 removing devices 16, 41, 51, 66 include the CO 2 separation membranes 20, 42, 52, 67 of the CO 2 facilitated transport membrane. film but at least any one of the CO 2 removing device 16,41,51,66 is not limited to this configuration, for example, having a CO 2 separation membrane other than CO 2 -facilitated transport membrane It may be a separation type configuration, a configuration employing a chemical absorption method, a PSA device, a TSA device, or the like.
- the amount of absorption liquid, the amount of circulation of the absorption liquid, and the like can be used as operating conditions that affect the increase and decrease of the carbon dioxide removal rate.
- the amount of adsorbent, pressure, and the like can be used as operating conditions that affect the increase and decrease of the carbon dioxide removal rate.
- the amount of adsorbent, temperature, and the like can be used as operating conditions that affect the increase and decrease of the carbon dioxide removal rate.
- the steam (water vapor) is supplied from the water vapor supply unit 18 to the mixed gas MG, but the mixed gas MG supplied to the fuel gas supply devices 13 and 13a is described. If steam is already contained therein, it is not necessary to supply steam to the mixed gas MG according to the configuration.
- the CO 2 removing devices 16, 41, 51, 66 include the CO 2 separation membranes 20, 42, 52, 67 of the CO 2 facilitated transport membrane, and the second treatment chamber
- the sweep gases SG, SG1, SG2 and SG3 are supplied into 22, 44, 45, and 69 to generate a partial pressure difference of CO 2 between the supply side and the permeation side of the CO 2 separation membranes 20, 42, 52, and 67.
- the second processing chamber 22, 44, of the sweep gas SG, SG1, SG2, SG3 in at least one of the CO 2 removal devices 16, 41, 51, 66 is assumed.
- the pressure in the first processing chambers 21, 43, 53, 68 of the CO 2 separation membranes 20, 42, 52, 67 is not supplied into the chambers 54, 69, or the second processing chambers 22, 44, 54 and reducing the pressure in 69, CO 2 separation membrane 2 ,
- a configuration may be adopted by the operation method that causes the CO 2 partial pressure difference between the permeate side and feed side of 42,52,67 (pressurized or vacuum type).
- a pressure reducing type in which the inside of the second processing chamber 22, 44, 44, 69 is depressurized, it is preferable to install a vacuum pump on the downstream side of the second processing chamber 22, 44, 54, 69.
- the configuration by the sweep gas method may be combined with the configuration by the pressure type or the pressure reduction type.
- the configuration by the sweep gas method is not used as the CO 2 removal device 16 and the configuration by the pressurization type or the pressure reduction type is adopted, the flow rate of the sweep gas SG (the sweep gas flow rate is Fs) not included.
- the use of the mixed gas derived from the biogas obtained by methane fermentation of the organic substance as the mixed gas MG is assumed, but the present invention is not necessarily limited to the mixed gas derived from the biogas It is not a thing.
- the mixed gas MG is not derived from biogas when it is a mixed gas mainly composed of methane and carbon dioxide and the concentration of methane and / or carbon dioxide can vary depending on the production conditions of the mixed gas, etc. Also, by using the present system 10, 10a, 10b, it is possible to suppress the concentration fluctuation.
- the first gas supply device 40 and the second gas supply device 50 since the first gas supply device 40 and the second gas supply device 50 respectively generate the first concentration adjustment gas BG1 and the second concentration adjustment gas BG2, CO 2 separation is performed.
- the case where the device 41 and the CO 2 separation device 51 are separately provided has been described.
- the CO 2 separation device 41 and the CO 2 separation device 51 do not necessarily need to be separately provided.
- the first gas supply device 40 and the second gas supply device 50 may be configured to include one CO 2 separation device.
- the power generation system of the present invention can be used for a power generation system equipped with a gas engine that consumes a fuel gas containing carbon dioxide mainly containing methane and generates kinetic energy.
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Abstract
Description
前記燃料ガス供給装置が、前記混合ガス中の二酸化炭素を除去する二酸化炭素除去装置と、前記二酸化炭素除去装置の二酸化炭素除去率の増減に影響する運転条件を制御する運転条件制御装置を備え、
前記ガス濃度センサが、前記二酸化炭素除去装置の前段及び後段の少なくとも何れか一方に配置され、
前記運転条件制御装置が、前記ガス濃度センサの計測結果に基づいて、前記二酸化炭素除去装置の前記運転条件を制御することにより、前記混合ガス中のメタンと二酸化炭素の濃度を制御することを第1の特徴とする。
前記第1処理室に、前記混合ガスを前記第1処理室内に受け入れる第1受入口と、前記対象成分ガスの濃度が制御された前記第1処理室内の前記混合ガスを前記燃料ガスとして排出する第1排出口が設けられ、
前記第2処理室に、前記二酸化炭素分離膜を介して前記第1処理室から前記第2処理室へ透過したガスを排出する第2排出口が設けられ、
前記運転条件制御装置が、前記二酸化炭素分離膜の二酸化炭素除去率の増減に影響する運転条件として、前記第1処理室内に供給される前記混合ガスの流量、前記第1処理室内の圧力、前記第2処理室内の圧力、前記二酸化炭素分離膜の周囲温度、及び、前記二酸化炭素分離膜の膜面積を含む制御対象運転条件候補の内の少なくとも1つを、前記ガス濃度センサの計測結果に基づいて制御することを第2の特徴とする。
前記第1ガス供給装置が、前記ガス濃度センサの計測結果に基づいて、前記対象成分ガスが二酸化炭素で、前記混合ガスの前記対象成分ガスの濃度が前記設定範囲より高い場合、または、前記対象成分ガスがメタンで、前記混合ガスの前記対象成分ガスの濃度が前記設定範囲より低い場合に、前記混合ガスに前記第1濃度調整ガスを供給して、前記混合ガス中のメタンと二酸化炭素の濃度を制御することを第7の特徴とする。
前記第2ガス供給装置が、前記ガス濃度センサの計測結果に基づいて、前記対象成分ガスが二酸化炭素で、前記混合ガスの前記対象成分ガスの濃度が前記設定範囲より低い場合、または、前記対象成分ガスがメタンで、前記混合ガスの前記対象成分ガスの濃度が前記設定範囲より高い場合に、前記混合ガスに前記第2濃度調整ガスを供給することを第8の特徴とする。
前記燃料ガス供給装置が、前記対象成分ガスが二酸化炭素の場合は前記設定範囲より前記対象成分ガスの濃度の低い、または、前記対象成分ガスがメタンの場合は前記設定範囲より前記対象成分ガスの濃度の高い、メタンを主成分とする第1濃度調整ガスを前記混合ガスに供給する第1ガス供給装置と、前記対象成分ガスが二酸化炭素の場合は前記設定範囲より前記対象成分ガスの濃度の高い、または、前記対象成分ガスがメタンの場合は前記設定範囲より前記対象成分ガスの濃度の低い、二酸化炭素またはメタンと二酸化炭素を主成分とする第2濃度調整ガスを前記混合ガスに供給する第2ガス供給装置と、を備え、
前記第1ガス供給装置が、前記ガス濃度センサの計測結果に基づいて、前記対象成分ガスが二酸化炭素で、前記混合ガスの前記対象成分ガスの濃度が前記設定範囲より高い場合、または、前記対象成分ガスがメタンで、前記混合ガスの前記対象成分ガスの濃度が前記設定範囲より低い場合に、前記混合ガスに前記第1濃度調整ガスを供給して、前記混合ガス中のメタンと二酸化炭素の濃度を制御し、
前記第2ガス供給装置が、前記ガス濃度センサの計測結果に基づいて、前記対象成分ガスが二酸化炭素で、前記混合ガスの前記対象成分ガスの濃度が前記設定範囲より低い場合、または、前記対象成分ガスがメタンで、前記混合ガスの前記対象成分ガスの濃度が前記設定範囲より高い場合に、前記混合ガスに前記第2濃度調整ガスを供給して、前記混合ガス中のメタンと二酸化炭素の濃度を制御することを第9の特徴とする。
最初に、第1実施形態に係る本システムの概略構成について図面を参照して説明する。図1は、本システム10の概略の構成例を模式的に示すブロック図である。
次に、本システムの第2実施形態について、図面を参照して説明する。
次に、本システムの第3実施形態について、図面を参照して説明する。
次に、上記第1~第3実施形態の変形例(別実施形態)について説明する。
11 : ガスエンジン
12 : 発電機
13,13a,60 : 燃料ガス供給装置
14,46,57,71,74: ガス濃度センサ
15 : インバータ装置
16,41,51,66 : CO2除去装置
17 : 運転条件制御装置
17a,61 : 制御部
18 : 水蒸気供給部
18a : 水蒸気分離部
19,47,55,72 : 水蒸気除去部
20,42,52,67 : CO2分離膜(CO2促進輸送膜)
21,43,53,68 : 第1処理室
21a : 第1受入口
21b : 第11排出口
22,44,54,69 : 第2処理室
22a : 第2受入口
22b : 第2排出口
23a : 第1供給管
23b : 第1排気管
24a : 第2供給管
24b : 第2排気管
25,28 : マスフローコントローラ
26,29 : 背圧弁
27,30 : 圧力計
31 : 流量調整装置
32 : 圧力調整装置
40,62 : 第1ガス供給装置
45,70 : 第1容器
50,63 : 第2ガス供給装置
56,73 : 第2容器
64 : ガス混合部
65 : 流量計
EG,EG’ : 混合ガス
FG : 燃料ガス
MG,MG’,MG1 : 混合ガス
SG,SG1,SG2,SG3: スイープガス
SG1’,SG2’,SG3’: 混合ガス
Claims (20)
- メタンを主成分として二酸化炭素を含む燃料ガスを消費して運動エネルギを発生するガスエンジンと、前記ガスエンジンが発生する前記運動エネルギにより駆動され発電する発電機を備えた発電システムであって、
外部から供給されるメタンと二酸化炭素を主成分とする混合ガスに対して、前記混合ガス中のメタンと二酸化炭素の少なくとも何れか一方の対象成分ガスの濃度を、前記ガスエンジンの前記燃料ガス中の前記対象成分ガスの濃度に対する設定範囲内に制御して、前記燃料ガスとして、前記ガスエンジンに供給する燃料ガス供給装置と、
前記混合ガスの二酸化炭素濃度とメタン濃度の少なくとも何れか一方の濃度を計測するガス濃度センサと、を更に備え、
前記燃料ガス供給装置が、前記混合ガス中の二酸化炭素を除去する二酸化炭素除去装置と、前記二酸化炭素除去装置の二酸化炭素除去率の増減に影響する運転条件を制御する運転条件制御装置を備え、
前記ガス濃度センサが、前記二酸化炭素除去装置の前段及び後段の少なくとも何れか一方に配置され、
前記運転条件制御装置が、前記ガス濃度センサの計測結果に基づいて、前記二酸化炭素除去装置の前記運転条件を制御することにより、前記混合ガス中のメタンと二酸化炭素の濃度を制御することを特徴とする発電システム。 - 前記二酸化炭素除去装置が、前記混合ガス中に含まれる二酸化炭素をメタンに対して選択的に分離する二酸化炭素分離膜と、前記二酸化炭素分離膜によって隔てられた第1処理室と第2処理室を備えて構成され、
前記第1処理室に、前記混合ガスを前記第1処理室内に受け入れる第1受入口と、前記対象成分ガスの濃度が制御された前記第1処理室内の前記混合ガスを前記燃料ガスとして排出する第1排出口が設けられ、
前記第2処理室に、前記二酸化炭素分離膜を介して前記第1処理室から前記第2処理室へ透過したガスを排出する第2排出口が設けられ、
前記運転条件制御装置が、前記二酸化炭素分離膜の二酸化炭素除去率の増減に影響する運転条件として、前記第1処理室内に供給される前記混合ガスの流量、前記第1処理室内の圧力、前記第2処理室内の圧力、前記二酸化炭素分離膜の周囲温度、及び、前記二酸化炭素分離膜の膜面積を含む制御対象運転条件候補の内の少なくとも1つを、前記ガス濃度センサの計測結果に基づいて制御することを特徴とする請求項1に記載の発電システム。 - 前記第2処理室が、スイープガスを前記第2処理室内に受け入れる第2受入口を有し、前記二酸化炭素分離膜を介して前記第1処理室から前記第2処理室へ透過したガスと前記スイープガスが前記第2排出口から排出されるように構成され、
前記制御対象運転条件候補に、前記第2処理室内に供給される前記スイープガスの流量が含まれていることを特徴とする請求項2に記載の発電システム。 - 前記二酸化炭素分離膜が、メタンと反応せずに二酸化炭素と選択的に反応する二酸化炭素キャリアが添加された促進輸送膜であり、
前記制御対象運転条件候補に、前記第1処理室内の相対湿度及び前記第2処理室内の相対湿度の少なくとも何れか一方の増減に影響する1以上の運転条件が含まれていることを特徴とする請求項2に記載の発電システム。 - 前記二酸化炭素分離膜が、メタンと反応せずに二酸化炭素と選択的に反応する二酸化炭素キャリアが添加された促進輸送膜であり、
前記制御対象運転条件候補に、前記第1処理室内の相対湿度及び前記第2処理室内の相対湿度の少なくとも何れか一方の増減に影響する1以上の運転条件が含まれていることを特徴とする請求項3に記載の発電システム。 - 前記第1処理室内に供給される前記混合ガスに水蒸気が含まれていることを特徴とする請求項4に記載の発電システム。
- 前記第1処理室内に供給される前記混合ガスに水蒸気を供給する水蒸気供給部を備えることを特徴とする請求項4に記載の発電システム。
- 前記第1処理室内に供給される前記混合ガス、及び、前記第2処理室内に供給される前記スイープガスの少なくとも何れか一方に水蒸気が含まれていることを特徴とする請求項5に記載の発電システム。
- 前記第1処理室内に供給される前記混合ガス、及び、前記第2処理室内に供給される前記スイープガスの少なくとも何れか一方に水蒸気を供給する水蒸気供給部を備えることを特徴とする請求項5に記載の発電システム。
- 前記運転条件制御装置が、
前記水蒸気供給部が前記混合ガスに水蒸気の供給する場合は、前記混合ガスに対する前記水蒸気供給部からの水蒸気添加量を、前記制御対象運転条件候補の1つとして制御し、
前記水蒸気供給部が前記スイープガスに水蒸気の供給する場合は、前記スイープガスに対する前記水蒸気供給部からの水蒸気添加量を、前記制御対象運転条件候補の1つとして制御することを特徴とする請求項7または9に記載の発電システム。 - 前記水蒸気供給部は、前記ガスエンジンから排出される高温の排出ガスとの熱交換により水を加熱して生成された水蒸気を、前記対象ガスに供給することを特徴とする請求項7、9及び10の何れか1項に記載の発電システム。
- 前記水蒸気供給部は、前記ガスエンジンから排出される排出ガスに含まれる水蒸気を、前記対象ガスに供給することを特徴とする請求項7、9、10及び11の何れか1項に記載の発電システム。
- 前記混合ガスが、有機物のメタン発酵により生成されたバイオガスに由来するガスを含み、前記混合ガス中に含まれる硫黄成分を除去する超高次脱硫触媒を用いた脱硫装置を、前記燃料ガス供給装置より上流側に備えることを特徴とする請求項4~12の何れか1項に記載の発電システム。
- 前記燃料ガス供給装置が、前記対象成分ガスが二酸化炭素の場合は前記設定範囲より前記対象成分ガスの濃度の低い、または、前記対象成分ガスがメタンの場合は前記設定範囲より前記対象成分ガスの濃度の高い、メタンを主成分とする第1濃度調整ガスを前記混合ガスに供給する第1ガス供給装置を備え、
前記第1ガス供給装置が、前記ガス濃度センサの計測結果に基づいて、前記対象成分ガスが二酸化炭素で、前記混合ガスの前記対象成分ガスの濃度が前記設定範囲より高い場合、または、前記対象成分ガスがメタンで、前記混合ガスの前記対象成分ガスの濃度が前記設定範囲より低い場合に、前記混合ガスに前記第1濃度調整ガスを供給して、前記混合ガス中のメタンと二酸化炭素の濃度を制御することを特徴とする請求項1~13の何れか1項に記載の発電システム。 - 前記第1ガス供給装置が、前記混合ガス中に含まれる二酸化炭素をメタンに対して選択的に分離する第2の二酸化炭素除去装置と、前記第2の二酸化炭素除去装置を用いて前記混合ガスから二酸化炭素を分離して予め準備した前記第1濃度調整ガスを貯蔵する第1容器と、を備えていることを特徴とする請求項14に記載の発電システム。
- 前記燃料ガス供給装置が、前記対象成分ガスが二酸化炭素の場合は前記設定範囲より前記対象成分ガスの濃度の高い、または、前記対象成分ガスがメタンの場合は前記設定範囲より前記対象成分ガスの濃度の低い、二酸化炭素またはメタンと二酸化炭素を主成分とする第2濃度調整ガスを前記混合ガスに供給する第2ガス供給装置を備え、
前記第2ガス供給装置が、前記ガス濃度センサの計測結果に基づいて、前記対象成分ガスが二酸化炭素で、前記混合ガスの前記対象成分ガスの濃度が前記設定範囲より低い場合、または、前記対象成分ガスがメタンで、前記混合ガスの前記対象成分ガスの濃度が前記設定範囲より高い場合に、前記混合ガスに前記第2濃度調整ガスを供給することを特徴とする請求項1~15の何れか1項に記載の発電システム。 - 前記第2ガス供給装置が、前記第2濃度調整ガスを貯蔵する第2容器を備え、
前記第2濃度調整ガスが、前記二酸化炭素除去装置によって前記混合ガスから除去された二酸化炭素を含むことを特徴とする請求項16に記載の発電システム。 - メタンを主成分として二酸化炭素を含む燃料ガスを消費して運動エネルギを発生するガスエンジンと、前記ガスエンジンが発生する前記運動エネルギにより駆動され発電する発電機を備えた発電システムであって、
外部から供給されるメタンと二酸化炭素を主成分とする混合ガスに対して、前記混合ガス中のメタンと二酸化炭素の少なくとも何れか一方の対象成分ガスの濃度を、前記ガスエンジンの前記燃料ガス中の前記対象成分ガスの濃度に対する設定範囲内に制御して、前記燃料ガスとして、前記ガスエンジンに供給する燃料ガス供給装置と、
前記混合ガスの二酸化炭素濃度とメタン濃度の少なくとも何れか一方の濃度を計測するガス濃度センサと、を更に備え、
前記燃料ガス供給装置が、前記対象成分ガスが二酸化炭素の場合は前記設定範囲より前記対象成分ガスの濃度の低い、または、前記対象成分ガスがメタンの場合は前記設定範囲より前記対象成分ガスの濃度の高い、メタンを主成分とする第1濃度調整ガスを前記混合ガスに供給する第1ガス供給装置と、前記対象成分ガスが二酸化炭素の場合は前記設定範囲より前記対象成分ガスの濃度の高い、または、前記対象成分ガスがメタンの場合は前記設定範囲より前記対象成分ガスの濃度の低い、二酸化炭素またはメタンと二酸化炭素を主成分とする第2濃度調整ガスを前記混合ガスに供給する第2ガス供給装置と、を備え、
前記第1ガス供給装置が、前記ガス濃度センサの計測結果に基づいて、前記対象成分ガスが二酸化炭素で、前記混合ガスの前記対象成分ガスの濃度が前記設定範囲より高い場合、または、前記対象成分ガスがメタンで、前記混合ガスの前記対象成分ガスの濃度が前記設定範囲より低い場合に、前記混合ガスに前記第1濃度調整ガスを供給して、前記混合ガス中のメタンと二酸化炭素の濃度を制御し、
前記第2ガス供給装置が、前記ガス濃度センサの計測結果に基づいて、前記対象成分ガスが二酸化炭素で、前記混合ガスの前記対象成分ガスの濃度が前記設定範囲より低い場合、または、前記対象成分ガスがメタンで、前記混合ガスの前記対象成分ガスの濃度が前記設定範囲より高い場合に、前記混合ガスに前記第2濃度調整ガスを供給して、前記混合ガス中のメタンと二酸化炭素の濃度を制御することを特徴とする発電システム。 - 前記燃料ガス供給装置が、前記混合ガス中に含まれる二酸化炭素をメタンに対して選択的に分離する二酸化炭素除去装置と、前記二酸化炭素除去装置を用いて前記混合ガスから二酸化炭素を分離して予め準備した前記第1濃度調整ガスと前記第2濃度調整ガスを各別に貯蔵する第1容器と第2容器を備えていることを特徴とする請求項18に記載の発電システム。
- 前記混合ガスが、有機物のメタン発酵により生成されたバイオガスに由来するガスを含むことを特徴とする請求項1~12、14~19の何れか1項に記載の発電システム。
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| EP3680470A1 (en) | 2020-07-15 |
| CN111094725A (zh) | 2020-05-01 |
| EP3680470A4 (en) | 2021-06-02 |
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| US11214746B2 (en) | 2022-01-04 |
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