GB2632689A - Method for operating a solid oxide fuel cell system and a solid oxide fuel cell system - Google Patents
Method for operating a solid oxide fuel cell system and a solid oxide fuel cell system Download PDFInfo
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- GB2632689A GB2632689A GB2312583.4A GB202312583A GB2632689A GB 2632689 A GB2632689 A GB 2632689A GB 202312583 A GB202312583 A GB 202312583A GB 2632689 A GB2632689 A GB 2632689A
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- 239000000446 fuel Substances 0.000 title claims abstract description 164
- 238000000034 method Methods 0.000 title claims abstract description 31
- 239000007787 solid Substances 0.000 title claims abstract description 22
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 32
- 239000001301 oxygen Substances 0.000 claims abstract description 32
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 32
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims abstract description 29
- 239000003546 flue gas Substances 0.000 claims abstract description 29
- 229910001868 water Inorganic materials 0.000 claims description 31
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 27
- 238000002485 combustion reaction Methods 0.000 claims description 14
- 238000004891 communication Methods 0.000 claims description 5
- 239000012530 fluid Substances 0.000 claims description 5
- 238000009835 boiling Methods 0.000 claims description 2
- 239000007789 gas Substances 0.000 abstract description 6
- 239000000306 component Substances 0.000 description 8
- 238000000926 separation method Methods 0.000 description 8
- 239000000203 mixture Substances 0.000 description 7
- 230000003647 oxidation Effects 0.000 description 6
- 238000007254 oxidation reaction Methods 0.000 description 6
- 238000005868 electrolysis reaction Methods 0.000 description 4
- 230000009919 sequestration Effects 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000009833 condensation Methods 0.000 description 3
- 230000005494 condensation Effects 0.000 description 3
- 238000000605 extraction Methods 0.000 description 3
- 238000012546 transfer Methods 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 238000013461 design Methods 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000005201 scrubbing Methods 0.000 description 2
- 238000000629 steam reforming Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000011144 upstream manufacturing Methods 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- GQPLMRYTRLFLPF-UHFFFAOYSA-N Nitrous Oxide Chemical class [O-][N+]#N GQPLMRYTRLFLPF-UHFFFAOYSA-N 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 238000002407 reforming Methods 0.000 description 1
- 239000002918 waste heat Substances 0.000 description 1
Classifications
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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
- H01M8/04—Auxiliary arrangements, e.g. for control of pressure or for circulation of fluids
- H01M8/04082—Arrangements for control of reactant parameters, e.g. pressure or concentration
- H01M8/04089—Arrangements for control of reactant parameters, e.g. pressure or concentration of gaseous reactants
- H01M8/04119—Arrangements for control of reactant parameters, e.g. pressure or concentration of gaseous reactants with simultaneous supply or evacuation of electrolyte; Humidifying or dehumidifying
- H01M8/04156—Arrangements for control of reactant parameters, e.g. pressure or concentration of gaseous reactants with simultaneous supply or evacuation of electrolyte; Humidifying or dehumidifying with product water removal
- H01M8/04164—Arrangements for control of reactant parameters, e.g. pressure or concentration of gaseous reactants with simultaneous supply or evacuation of electrolyte; Humidifying or dehumidifying with product water removal by condensers, gas-liquid separators or filters
-
- 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
- H01M8/0662—Treatment of gaseous reactants or gaseous residues, e.g. cleaning
-
- 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
- H01M8/04—Auxiliary arrangements, e.g. for control of pressure or for circulation of fluids
- H01M8/04007—Auxiliary arrangements, e.g. for control of pressure or for circulation of fluids related to heat exchange
- H01M8/04014—Heat exchange using gaseous fluids; Heat exchange by combustion of reactants
-
- 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
- H01M8/04—Auxiliary arrangements, e.g. for control of pressure or for circulation of fluids
- H01M8/04007—Auxiliary arrangements, e.g. for control of pressure or for circulation of fluids related to heat exchange
- H01M8/04014—Heat exchange using gaseous fluids; Heat exchange by combustion of reactants
- H01M8/04022—Heating by combustion
-
- 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
- H01M8/04—Auxiliary arrangements, e.g. for control of pressure or for circulation of fluids
- H01M8/04082—Arrangements for control of reactant parameters, e.g. pressure or concentration
- H01M8/04089—Arrangements for control of reactant parameters, e.g. pressure or concentration of gaseous reactants
- H01M8/04097—Arrangements for control of reactant parameters, e.g. pressure or concentration of gaseous reactants with recycling of the reactants
-
- 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
- H01M8/0606—Combination of fuel cells with means for production of reactants or for treatment of residues with means for production of gaseous reactants
- H01M8/0612—Combination of fuel cells with means for production of reactants or for treatment of residues with means for production of gaseous reactants from carbon-containing material
- H01M8/0618—Reforming processes, e.g. autothermal, partial oxidation or steam reforming
-
- 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
- H01M8/0662—Treatment of gaseous reactants or gaseous residues, e.g. cleaning
- H01M8/0668—Removal of carbon monoxide or carbon dioxide
-
- 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
- H01M8/10—Fuel cells with solid electrolytes
- H01M8/12—Fuel cells with solid electrolytes operating at high temperature, e.g. with stabilised ZrO2 electrolyte
-
- 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
- H01M8/10—Fuel cells with solid electrolytes
- H01M8/12—Fuel cells with solid electrolytes operating at high temperature, e.g. with stabilised ZrO2 electrolyte
- H01M2008/1293—Fuel cells with solid oxide electrolytes
-
- 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
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/30—Hydrogen technology
- Y02E60/50—Fuel cells
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- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Sustainable Development (AREA)
- Manufacturing & Machinery (AREA)
- Sustainable Energy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Combustion & Propulsion (AREA)
- Fuel Cell (AREA)
Abstract
A method of operating a solid oxide fuel cell system may comprise providing a fuel feed stream (FF) to a fuel cell module 4, the fuel cell module expelling an exhaust fuel stream (EF). An air feed stream (AF) may also be provided to the module 4 which expels an air exhaust stream (EA). At least a portion of the exhaust fuel stream (EF) may be fed to an afterburner 26, along with oxygen from an oxygen source 28, and the exhaust fuel stream (EF) and the oxygen may be burned in a stoichiometric ratio. Flue gas (FG) from the afterburner 26 may be used in a superheater 30 to super heat the exhaust gas stream (EA). Heat from the exhaust air stream (EA) may be used to heat the fuel (FF) or air (AF) feed streams. The fuel cell system is also disclosed.
Description
Description
Method for operating a solid oxide fuel cell system and a solid oxide fuel cell system The invention relates to a method for operating a solid oxide fuel cell (SOFC) system, comprising the steps of providing a fuel feed stream to a fuel cell module and the fuel cell module expelling an exhaust fuel stream, and providing an air feed stream to the fuel cell module and the fuel cell module expelling an exhaust air stream.
The invention also relates to a solid oxide fuel cell system comprising a fuel cell module configured to receive a fuel feed stream from a fuel feed line and to expel an exhaust fuel stream through an exhaust fuel line, also configured to receive an air feed stream from an air feed line and to expel an exhaust air stream through an exhaust air line.
The separation of CO_ from the exhaust gas of fuel cell systems based on the oxidation of hydrocarbons using conventional methods (e.g., amine scrubbing) is complex and energy intensive. The reason for this lies in the oxidation of the fuel with a clear excess of air. Downstream of the fuel cell, the exhaust gas is mixed with the air and the unreacted fuel components are oxidized. This results in a flue gas in which CO: takes up a smaller volume fraction alongside the other components (N2, H2O, etc.). Due to the strong dilution of CO-, its separation is quite complex and requires a high system complexity, additional operating materials (e.g., amine) and/or higher energy consumption. The separation of 002 may also take place under efficiency losses of the system (e.g., drive of pumps, pressure losses, etc.) and the purity of the separated CO2 is limited in a single-stage process.
At present, the most common methods for CO; separation involve the removal of CO2 after an oxidation process (usually combustion) using air. This is often based on a fuel/air-mixture with excess air (post-combustion carbon capture). As a result, the 002 is present in the flue gas in relatively low concentrations, and it takes great efforts to remove it. The efforts, costs and loss of efficiency are significant.
Moreover, it is not possible to separate the CO2 completely in one step. In addition, there are possible environmental impacts due to the used operating materials (e.g., amine scrubbing of the flue gas).
Other methods involve stoichiometric oxidation with oxygen and downstream separation of the water content by condensation. These methods are applied at high temperatures and hence, the components are exposed to high temperature stress. In some cases, the high temperatures are lowered by using the reaction products as working media in a heat exchange process.
US20220246966A1 describes a solid oxide fuel cell (SOFC) system with carbon capture. The system includes an afterburner in fluid communication with the fuel cell module and disposed downstream of the outlet. The SOFC module outputs oxygen depleted air and depleted fuel streams. The depleted fuel stream is routed to an output manifold, wherein a first portion of the depleted fuel is sent to the fluidly coupled af-terburner and a second portion of the depleted fuel forms a recycle stream back to the fuel inlet manifold. The afterburner, which also receives depleted air, is configured to facilitate the combustion of the remaining oxidant from the depleted air and the first portion of the depleted fuel in order to produce an exhaust stream, which includes CO_, nitrous oxides (NOx), nitrogen (N;), and H2O.
The object of the invention is to provide an improved system for separation of CO_ from the exhaust gas of solid oxide 35 fuel cell systems.
The object of the invention is achieved by the independent claims. The dependent claims describe advantageous developments and modifications of the invention.
In accordance with the invention there is provided a method for operating a solid oxide fuel cell system, comprising the steps of: - providing a fuel feed stream to a fuel cell module and the fuel cell module expelling an exhaust fuel stream, -providing an air feed stream to the fuel cell module and the fuel cell module expelling an exhaust air stream, wherein - feeding at least a portion of the exhaust fuel stream to an afterburner, feeding in the afterburner oxygen from an oxygen source and burning the exhaust fuel stream and the oxygen in a stochiometric ratio, - using flue gas from the afterburner in a superheater to superheat the exhaust air stream.
In accordance with the invention there is also provided a fuel cell system comprising: - a fuel cell module configured to receive a fuel feed stream from a fuel feed line and to expel an exhaust fuel stream through an exhaust fuel line, also config-ured to receive an air feed stream from an air feed line and to expel an exhaust air stream through an exhaust air line, wherein - an afterburner in fluid communication with the fuel cell module, wherein the afterburner is configured to receive at least a portion of the exhaust fuel stream and is al-so connected to an oxygen source, wherein the afterburner is configured for stochiometric combustion of the exhaust fuel stream and the oxygen, and - a superheater arranged on the exhaust air line and in fluid communication with a flue gas line from the after-burner, wherein the superheater is configured to superheat the exhaust air stream using flue gas from the afterburner.
The essential idea of the present invention is the combination of a stoichiometric oxy-fuel post-combustion with a solid oxide fuel cell module. Stoichiometric combustion means that an optimum oxygen and fuel mix levels lead to maximum combustion efficiency. In the afterburner, at least part of the exhaust fuel stream is mixed with an external pure or almost pure oxygen (i.e., the oxygen stream used in the afterburner is different from the air feed stream or the exhaust air stream). The oxygen for the oxy-fuel combustion can originate from an air separation process or an electrolysis process. The oxygen extraction can take place separately and/or with a time delay to the fuel cell operation. This means, that as the oxygen feed is low, oxygen tanks could be used for longer operation periods. One great advantage of the suggested method for operating a solid oxide fuel cell system is that the low proportion of fuel and the high proportion of reaction components in the exhaust fuel stream result in moderate combustion temperatures as well as in reduced oxygen demand.
The oxygen demand is significantly reduced by the installation of the stoichiometric, electrochemically controlled oxidation process downstream of the SOFC module and the catalyt-is stoichiometric oxy-fuel combustion. Furthermore, compressed oxygen or oxygen extraction systems require considerably smaller system sizes. Using oxygen from an electrolysis process, results in the recovery of the electrolysis energy used for CO2 sequestration (instantly or with a time delay).
As the extraction of oxygen also requires energy, its quantity is also reduced.
The reuse of the heat from the oxyfuel combustion at various points in the SOFC system significantly reduces the loss of efficiency due to the CO1 sequestration process. The separated products CO2 and water, at the end of the process, are almost in pure form. This opens possibilities for direct recycling. Due to the fuel flexibility of an SOFC system, renewa-ble hydrocarbon sources can be used (e.g., biogas). In such a case, CO2 can be removed from the atmosphere (biogas) with little effort using the suggested method. The efforts involved and the loss of efficiency are considerably lower than with the present methods known from the prior art. Due to the two-stage oxidation process at moderate temperatures, the component load is lower than with single-stage high-temperature oxyfuel combustion without an upstream SOFT module.
Preferably, the flue gas is cooled below the boing point of water in a water condenser downstream of the superheater. For this purpose, a water condenser is arranged downstream of the superheater. The reaction products leaving the catalytic af-terburner are a mixture of superheated water vapour and CO2. To separate the CO-from the water vapour, the water must be condensed out.
In a preferred embodiment, the heat from the flue gas is uti-lized to preheat the fuel feed stream. The condensation heat is thereby transferred to the fuel and preheats in a first step. With regard to the system design this means that the fuel feed line is connected to the water condenser and the water condenser is configured to utilize the heat from the flue gas to preheat the fuel feed stream.
In a preferred embodiment, which aims at on optimal use of the heat sources within the fuel cell system, the heat from the exhaust air stream is utilized to preheat the fuel feed stream. For this purpose, a fuel preheater is arranged on the fuel feed line and the fuel preheater is connected to the exhaust air line and configured to utilize the heat from the exhaust air stream to preheat the fuel feed stream. The pre-heater raises the fuel temperature to a higher temperature level.
Preferably, the high temperature of the exhaust air stream is further used, whereby the heat from the exhaust air stream is utilized to preheat the air feed stream. For this purpose, an air preheater is arranged on the air feed line and the air preheater is connected to the exhaust air line and configured to utilize the heat from the exhaust air stream to preheat the air feed stream.
In a preferred embodiment, the exhaust fuel stream is split into a first part, which is directed to the afterburner, and a second part, which is mixed with the fuel feed stream.
Therefore, the system comprises manifolds downstream from the fuel cell module, configured to split the exhaust fuel stream into a first part directed to the afterburner and a second part remaining in the exhaust fuel line, which is fluidly coupled to the fuel feed line. This way the unreacted fuel fraction is recycled, steam for the reforming process is provided and also part of the heat is reutilized.
In another preferred embodiment, in a last step before entering the fuel module, the fuel feed stream passes through a reformer. In the reformer, which is integrated in the fuel feed line before the fuel cell module, the excess thermal energy is partly bound in chemical fuel energy by a steam reforming process. The so-called reformate leaves the pre-reformer at the temperature level for the SOFC module.
An embodiment of the invention is now described, by way of example only, with reference to the accompanying drawing, of which the only figure shows a SOFO system with CO sequestration.
The system design in the figure shows the components of an SOFC system 2 with subsequent carbon capture (CO2 sequestration). An air feed stream AF is delivered to the cathode side of a solid oxide fuel cell module 4 via the blower 6 arranged on an air feed line 8. As the air feed stream AF passes through the air preheater 10 and is heated to the inlet temperature. The heat transfer takes place via the heat transfer surface of the air preheater 10 from the hot side to the air feed stream AF. The heated air feed stream AF passes the cathode of the SOFC module 4 and releases its oxygen stoichiometrically to the anode side of the SOFC module 4 through an electrolyte.
On the fuel side, a fuel feed stream FF in fuel feed line 16 is first directed to a water condenser 12 shown by the arrow Fl. There the fuel feed stream FF absorbs the condensation heat and is thereby preheated for the first time. The pre-heated fuel feed stream FF leaves the condenser 12, as shown by F2, and enters a fuel preheater 14, which is arranged on the fuel feed line 16. In the fuel preheater 14 the fuel temperature is raised to a yet higher temperature level. After leaving the fuel preheater 14, in manifolds 18 the fuel feed stream FF is mixed with a recirculate of an exhaust fuel stream EF, which contains mixture of steam, CO; and unreacted fuels, and finally passes through the reformer 20. There, the excess thermal energy is partly bound in chemical fuel energy by a steam reforming process. A mixture of CO2, CO, H20, FL:, CH4, called reformate, leaves the reformer 20 at the temperature level required for SOFC module 4.
In the SOFC module 4, part of the reformate is converted electrochemically and stoichiometrically at operating temper-ature of approx. 500-1000°C. The proportion of water vapour and CO2 is increased and at the same time the proportion of the fuel components such as H2, CO and CH4 is reduced. The conversion takes place at a maximum of 60-80%. An exhaust fuel stream EF containing low-calorific anode exhaust gas, which is highly enriched with water vapour and CO2, leaves the anode side of the SOFC fuel cell module 4 via an exhaust fuel line 21. The exhaust fuel stream EF is then split into two parts in manifolds 22. Part of this exhaust fuel stream ET is recirculated through the exhaust fuel line 21 upstream and fed back to the reformer 20 using a recirculation blower 24. About 60% of the exhaust fuel stream EF is recycled this way.
The other part of the exhaust fuel stream EF is fed into a afterburner 26, where it is stoichiometrically oxidized with oxygen in a catalytically supported process. Due to the low proportion of fuel and the high proportion of reaction compo-nents such as CO2 and H2O, the process takes place at moderate temperatures and the oxygen demand is low. The oxygen for the combustion process is provided from an oxygen source 28. The oxygen can be provided from an air separation process or from an electrolysis process carried out outside the SOFC 10 system 2.
The flue gas FG leaving the catalytic afterburner 26 through a flue gas line 29 contains a mixture of superheated water vapour and CO_. The heat energy in the flue gas FG leaving the oxyfuel combustor is exchanged with several media in cascading sequence. To separate the CO-from the water vapour, the water must be condensed out and discharged as a liquid phase. First, in s superheater 30, the excess thermal energy stored in the flue gas FG is transferred to the exhaust air stream EA coming from the SOFC module 4 through an exhaust air line 31, thus superheating the exhaust air stream EA. The exhaust air stream EA, in turn, transfers the thermal energy as a hot gas stream in the fuel preheater 14 to the fuel feed stream FF and in the air preheater 10 to the air feed stream AF, wherein the fuel preheater 14 and the air preheater 10 are both arranged on the exhaust air line 31.
The water vapour / CO, mixture exiting the superheater 30 is cooled in the condenser 12 below the boiling point of the wa- ter while transferring heat to the fuel feed stream FF, as explained above. Depending on the thermal equilibrium situation, additional heat exchangers could be provided for further waste heat utilisation. Water and CO-are present in almost pure form. The water is discharged into a water reser-voir 32 and the CO2 is stored in a CO2 reservoir 34. In general, the solid oxide fuel cell system 2 is designed for an optimal reuse of the heat contained in the system.
Claims (14)
- Patent claims 1. A method for operating a solid oxide fuel cell system (2), 5 comprising the steps of: - providing a fuel feed stream (FF) to a fuel cell module (4) and the fuel cell module (4) expelling an exhaust fuel stream (EF), - providing an air feed stream (AF) to the fuel cell module (4) and the fuel cell module (4) expelling an ex-haust air stream (EA), wherein - feeding at least a portion of the exhaust fuel stream (EF) to an afterburner (26), feeding in the afterburner (26) oxygen from an oxygen source (28) and burning the exhaust fuel stream (EF) and the oxygen in a stochio-metric ratio, - using flue gas (FG) from the afterburner (26) in a superheater (30) to superheat the exhaust air stream (EA).
- 2. The method according to claim 1, wherein the flue gas (FG) is cooled below the boing point of water in a water condenser (12) downstream of the superheater (30).
- 3. The method according to claim 2, wherein the heat from the 25 flue gas (FG) is utilized to preheat the fuel feed stream (FF).
- 4. The method according to any of the preceding claims, wherein the heat from the exhaust air stream (EA) is utilized 30 to preheat the fuel feed stream (FF).
- 5. The method according to any of the preceding claims, wherein the heat from the exhaust air stream (EA) is utilized to preheat the air feed stream (AT).
- 6. The method according to any of the preceding claims, wherein the exhaust fuel stream (EF) is split into a first part, which is directed to the afterburner (26), and a second part, which is mixed with the fuel feed stream (FF).
- 7. The method according to any of the preceding claims, 5 wherein before entering the fuel module (4), the fuel feed stream (FF) passes through a reformer (20).
- 8. A solid oxide fuel cell system (2) comprising: -a fuel cell module (4) configured to receive a fuel feed stream (FF) from a fuel feed line (16) and to expel an exhaust fuel stream (AF) through an exhaust fuel line (21), also configured to receive an air feed stream (AF) from an air feed line (8) and to expel an exhaust air stream (EA) through an exhaust air line (31), wherein -an afterburner (26) in fluid communication with the fuel cell module (4), wherein the afterburner (26) is configured to receive at least a portion of the exhaust fuel stream (EF) and is also connected to an oxygen source (28), wherein the afterburner (26) is configured for stochiometric combustion of the exhaust fuel stream (EF) and the oxygen, and a superheater (30) arranged on the exhaust air line (31) and in fluid communication with a flue gas line (29) from the afterburner (26), wherein the superheater (30) is configured to superheat the exhaust air stream (EA) using flue gas (FG) from the afterburner (26).
- 9. The solid oxide fuel cell system (2) according to claim 8, wherein a water condenser (12) is arranged on the flue gas line (29) downstream of the superheater (30) and the water condenser (12) is configured to cool the flue gas (FS) below the boiling point of water.
- 10. The solid oxide fuel cell system (2) according to claim 9, wherein the fuel feed line (16) is connected to the water condenser (12) and the water condenser (12) is configured to utilize the heat from the flue gas (FG) to preheat the fuel feed stream (FF).
- 11. The solid oxide fuel cell system (2) according to any of the claims 8 or 10, wherein a fuel preheater (14) is arranged on the fuel feed line (16) and the fuel preheater (14) is connected to the exhaust air line (31) and configured to utilize the heat from the exhaust air stream (EA) to preheat the fuel feed stream (FF).
- 12. The solid oxide fuel cell system (2) according to any of the preceding claims, wherein an air preheater (10) is arranged on the air feed line (8) and the air preheater (10) is connected to the exhaust air line (31) and configured to utilize the heat from the exhaust air stream (EA) to preheat the air feed stream (AF).
- 13. The solid oxide fuel cell system (2) according to any of the preceding claims, comprising manifolds (22) downstream from the fuel cell module (4), configured to split the exhaust fuel stream (EF) into a first part directed to the af-terburner (26) and a second part remaining in the exhaust fuel line (21), which is fluidly coupled to the fuel feed line (16).
- 14. The solid oxide fuel cell system (2) according to any of 25 the preceding claims, comprising a reformer (20) integrated in the fuel feed line (16) before the fuel cell module (4).
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2312583.4A GB2632689A (en) | 2023-08-17 | 2023-08-17 | Method for operating a solid oxide fuel cell system and a solid oxide fuel cell system |
| AU2024324249A AU2024324249A1 (en) | 2023-08-17 | 2024-07-26 | Method for operating a solid oxide fuel cell system and a solid oxide fuel cell system |
| PCT/EP2024/071318 WO2025036682A1 (en) | 2023-08-17 | 2024-07-26 | Method for operating a solid oxide fuel cell system and a solid oxide fuel cell system |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2312583.4A GB2632689A (en) | 2023-08-17 | 2023-08-17 | Method for operating a solid oxide fuel cell system and a solid oxide fuel cell system |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| GB202312583D0 GB202312583D0 (en) | 2023-10-04 |
| GB2632689A true GB2632689A (en) | 2025-02-19 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB2312583.4A Pending GB2632689A (en) | 2023-08-17 | 2023-08-17 | Method for operating a solid oxide fuel cell system and a solid oxide fuel cell system |
Country Status (3)
| Country | Link |
|---|---|
| AU (1) | AU2024324249A1 (en) |
| GB (1) | GB2632689A (en) |
| WO (1) | WO2025036682A1 (en) |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4128700A (en) * | 1977-11-26 | 1978-12-05 | United Technologies Corp. | Fuel cell power plant and method for operating the same |
| US4678723A (en) * | 1986-11-03 | 1987-07-07 | International Fuel Cells Corporation | High pressure low heat rate phosphoric acid fuel cell stack |
| US6331366B1 (en) * | 1999-06-23 | 2001-12-18 | International Fuel Cells Llc | Operating system for a fuel cell power plant |
| US20060188761A1 (en) * | 2005-01-25 | 2006-08-24 | O'brien Christopher J | Fuel cell power plants |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2004064220A2 (en) * | 2003-01-14 | 2004-07-29 | Shell Internationale Research Maatschappij B.V. | Process for generating electricity and concentrated carbon dioxide |
| DE102006046257A1 (en) * | 2006-09-28 | 2008-04-10 | J. Eberspächer GmbH & Co. KG | The fuel cell system |
| KR20230113769A (en) | 2020-12-04 | 2023-08-01 | 버사 파워 시스템스 리미티드 | Solid Oxide Fuel Cell Systems with Carbon Capture and Increased Efficiency |
-
2023
- 2023-08-17 GB GB2312583.4A patent/GB2632689A/en active Pending
-
2024
- 2024-07-26 WO PCT/EP2024/071318 patent/WO2025036682A1/en active Pending
- 2024-07-26 AU AU2024324249A patent/AU2024324249A1/en active Pending
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4128700A (en) * | 1977-11-26 | 1978-12-05 | United Technologies Corp. | Fuel cell power plant and method for operating the same |
| US4678723A (en) * | 1986-11-03 | 1987-07-07 | International Fuel Cells Corporation | High pressure low heat rate phosphoric acid fuel cell stack |
| US6331366B1 (en) * | 1999-06-23 | 2001-12-18 | International Fuel Cells Llc | Operating system for a fuel cell power plant |
| US20060188761A1 (en) * | 2005-01-25 | 2006-08-24 | O'brien Christopher J | Fuel cell power plants |
Also Published As
| Publication number | Publication date |
|---|---|
| GB202312583D0 (en) | 2023-10-04 |
| WO2025036682A1 (en) | 2025-02-20 |
| AU2024324249A1 (en) | 2026-02-12 |
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