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    • 专利摘要:
    The present invention relates to an apparatus for generating power having a plurality of tubular solid oxide fuel cells (2) contained in a reaction chamber (40). The fuel cell 2 is fixed to one end of the manifold and freely passes through the opening 63 of the baffle plate 47 so that the other end is in the combustion chamber 41. Reaction gas 41 surrounds the outside of the fuel cell from the plenum chamber 42 below the manifold block 50 through the inside of the tubular fuel cell 2 and a tubular inlet passage that may have a reforming catalyst. Is supplied. The gas inlet passage to the plenum chamber 42 and the annular inlet passage surrounding the reaction chamber are in heat transfer relationship with the reaction chamber, and the combustion chamber appropriately raises the gas to the reforming temperature and the reaction temperature.
    公开号:KR20010030874A
    申请号:KR1020007003566
    申请日:1998-10-01
    公开日:2001-04-16
    发明作者:새머스니겔마크
    申请人:조나단 알. 우드；아쿠멘트릭스 코포레이션；
    IPC主号:
    专利说明:

    Integrated Solid Oxide Fuel Cells and Modifiers {INTEGRATED SOLID OXIDE FUEL CELL AND REFORMER}
    SOFCs are electrochemical devices that can generate direct current electricity by electrochemically combining oxidants (such as air) with fuels (eg, hydrogen, natural gas, coal gas or other hydrocarbon-based fuels). The SOFC consists of an oxygen ion conducting electrolyte (currently stabilized zirconia-based) that separates the air electrode (cathode) and the fuel electrode (anode). The fuel is oxidized at the anode, and the electrons are released to an external circuit whereby the cathode in the external circuit is The cathode reaction reduces the oxidizing gas to oxygen ions, where the oxygen ions are transported to the anode through an oxygen ion conducting electrolyte, with electrons moving around their external circuitry (usually 1 volt in a single cell). As a load is applied through the cell, current flows to produce a power density, the value of which depends on the design of the cell and the material used. The cell is typically between 700 and 1000 degrees Celsius. N. Q. Min and T. Takahashi's excuses were "Science and Technology of Ceramic Fuel Cells" (Arms, 1995). Terdam Elsevier, describes the principle of reaction and the generation of electricity in SOFC.
    The biggest feature of SOFC is that it has high conversion efficiency (typically 50 to 90% when accompanied with heat utilization), produces less emissions, produces higher grade exhaust heat, From several kilowatts to several megawatts) of modularity.
    In general, single SOFC cells are stacked using interconnecting plates or bipolar plates (usually based on doped lanthanum chromite or hot metal systems) to create multi-cell units. A single cell typically produces 1 volt, but a predetermined voltage can be obtained by stacking single cells in parallel or series connections. Several structures of SOFCs are known, including planar, tubular, and monolithic designs. However, besides these three main designs, it should be noted that other designs in which the oxygen ion conductive electrolyte separates the fuel gas (at the anode) and the oxidizing gas (at the cathode) are used. For example, N.Q., a publication of the American Ceramic Society. See Min's paper on “Ceramic Fuel Cells” (76 [3] 1993), pages 563-588.
    In order for an SOFC system to be fully implemented and fully commercial, the SOFC system must be reliable for a long time and no thermal cracking due to heating or cooling cycles occurs. In addition, the system must compete with the prior art, such as gas turbines and diesel generators, and therefore must be relatively inexpensive and easy to assemble. The major drawbacks of current designs are mainly based on the sealability of a single cell. Although a flat design using a flat plate electrolyte with anodes and cathodes attached to each side appears to be the cheapest in terms of manufacturing cost, its main disadvantages are the problem of sealing the plate without causing excessive stress on the ceramic plate and the sealant and There is a chemical compatibility problem between the cells. The tubular design overcomes the sealing problem well by using closed or open end tubes. In conventional tubular designs, extruded and porous doped lanthanum manganite support tubes were made. The electrolyte (stabilized zirconia) is electrochemically deposited on a support tube. At this time, the anode is slurry spray-electrochemically deposited in the electrolyte, and the doped lanthanum chromite is plasma sprayed into the cell as an interconnect material. At this time, the batteries are classified into a multi-cell type unit and then manufactured as an SOFC system. Air is pumped into the tubes and the outside of the tube is exposed to the fuel gas. The tubes are sealed at one end so that spent air can flow back through the annulus. Spent fuel can also be recycled for heat recovery.
    This tubular structure has been very successful. However, this design does not allow rapid thermal cycling since the thermal stresses causing cracks in the cells can occur. Although improvements were attempted, the current limit in this design required 5 hours for the system to reach operating temperature of 1000 ° C. from ambient. Current-level generators using the aforementioned techniques are disclosed in US Pat. No. 5,244,752. This patent is a significant improvement over the SOFC systems cited in US Pat. Nos. 4,374,184, 4,395,468, 4,664,986, 4,729,931 and 4,751,152. The design described above is likewise expensive and does not help to produce small systems (10 kW or less). Manufacturers of those systems have reduced the cost of raw materials by reducing raw material costs. For example, 90% of the weight of the cell is on the doped lanthanum chromite air electrode, so the cost can be substantially reduced by supplying the raw material (high purity level) at a lower cost. These findings are listed in the Solid Oxide Fuel Cell Volume 5, pages 37-50 (1997) of the Electrochemical Society (New Jersey). It is described in Singal's paper "The Recent Progress of Tubular Solid Oxide Fuel Cell Technology." However, the cost of the system was also not taken into account for small productions.
    In order to solve the high manufacturing cost problem, the use of extruded thin walled stabilized zirconia tubes has been disclosed. See Australian Patent 675122. In that design the inner electrode was the fuel electrode, while the outer electrode was the air electrode (usually lanthanum manganate). In that design, the tubes were supported in a thermal insulated container, and exhaust gas could be discharged through the passage from the thermal insulated container. In that design, the cost of the tube was reduced by using a simple extrusion technique, for example, by extruding stabilized zirconia mixed with polyvinyl butyral and cyclohexane. The design is described as including an arrangement of the aforementioned tubes that is supported in a thermal insulated vessel through which combustion products can be discharged through the passage. Gas is fed directly to the top of the tubes. The combustion product is discharged through the same passage as the forced air inlet. Although this design is very simple, the design does not sufficiently take into account the movement in the cells in the reactor, and thus can easily increase the stress in the cell and cause cell breakage.
    In addition, the design described above did not have the capability to reform fuel in SOFC generators. Reforming is an operation in which a fuel (usually a hydrocarbon fuel in this case) is mixed with water and / or carbon dioxide to produce carbon monoxide and hydrogen. At this time, such reformed fuel is used directly in the SOFC system. In many cases, the fuel is reformed outside the SOFC generator, which requires expensive equipment such as heat exchangers, pumps and the like, and makes the entire system larger. The reforming reaction is quite undesirable when it occurs outside the generator, because a lot of energy (heat) is lost from the system, resulting in overall system efficiency and more complex device configuration. This problem is partially solved in US Pat. No. 4,729,931, which performs the step of reforming reformable gaseous fuel in an SOFC generator. In this system, partially consumed fuel is separated into two streams. A portion thereof is mixed with the partially consumed air stream to form an exhaust gas, at which time a portion leaks out, and then a portion of the residual exhaust gas is mixed with the secondary spent fuel stream. The combined flow is then mixed with the gaseous reformable fuel. The invention utilizes heat balance manipulation throughout the system to minimize heat loss. The invention uses a conventional design of a tubular SOFC system as disclosed in the aforementioned US patents, and therefore does not solve the initial problems such as system complexity, cost, thermal cycling performance at fast heating and cooling rates. In addition, the system is quite complex in configuration.
    Another design is disclosed in US Pat. No. 3,377,703. Here, some electrolyte tubes are installed upright on the ceramic base. The gas passes through the tubes and burns off the tops of the tubes. At this time, the hot gas flows to the heat exchanger around the system. Although the system is relatively simple, it requires a large number of high temperature seals and does not take into account the high thermal stresses that can be encountered in a quick start-up phase.
    TECHNICAL FIELD The present invention relates to a power generating apparatus, and more particularly, to an apparatus using solid oxide fuel cells (SOFC).
    DESCRIPTION OF THE EMBODIMENTS Preferred embodiments of the present invention will be described with reference to the accompanying drawings.
    1 is a partial side cross-sectional view schematically showing a power generating device according to an embodiment of the present invention.
    2 is a side cross-sectional view of a mounted fuel cell according to a preferred embodiment of the present invention.
    3 is a side cross-sectional view showing a plurality of mounted fuel cells and a supporting structure connected thereto according to an embodiment of the present invention.
    4 is a side cross-sectional view of a plurality of fuel cells mounted as a bundle in accordance with another embodiment of the present invention.
    5 is a partial side cross-sectional view schematically showing a power generating device according to a preferred embodiment of the present invention.
    It is therefore an object of the present invention to provide a power generating device using a solid oxide fuel cell which provides an alternative that overcomes the above mentioned disadvantages and allows the public to make useful choices.
    In one aspect, the invention includes an apparatus for generating power. The apparatus comprises a plurality of tubular solid oxide fuel cells disposed in a reaction chamber, each having an inward reaction surface and an outward reaction surface, and electrodes coupled with the respective surfaces, one end of which is mounted in a manifold block; A first gas inlet passage for supplying a first gas passing along the outside of the fuel cell to the reaction chamber and a second gas inlet passage for supplying a second gas to a mounting end of the fuel cell to pass along the inside of the fuel cell; And an exhaust gas outlet passage from the reaction chamber adjacent to an end of the fuel cell which can be uncombusted with each other and spaced apart from the manifold block for transporting the exhaust gas to the outlet, the interior of the fuel cell and A power collecting means for connecting said conductor on the outside; One of the first and second gases is a reforming fuel gas, the other is an oxidizing gas, and the gas passages are for respectively carrying one of the reformable gas or the oxidizing gas according to the arrangement of the reaction surface of the fuel cell; The reformable gas delivery passage has a reformable catalyst therein and is disposed in heat transfer relationship with the exhaust gas passage and the reaction chamber such that in steady state operation the temperature of the gas can be raised to the temperature of the catalyst that can be reformed; The oxidizing gas delivery passage is arranged in heat transfer relationship with the exhaust gas passage and the reaction chamber so that the gases inside can be raised to the temperature of the fuel cell in which the fuel cell operates in steady state operation.
    Each tubular fuel cell has an outer diameter of between 3 and 10 mm and a wall thickness of between 0.3 and 1.0 mm.
    Variable flow restricting means may be provided in the oxidizing gas inlet passage to control the combustion temperature by variably restricting the flow of the oxidizing gas into the fuel cell and the combustion zone.
    The second gas inlet passage is partially provided with a cylindrical or conical chamber, and the exhaust gas outlet passage is coaxial with the inlet passage and is generally cylindrical by a wall of aluminum or mullite material and having a thermal impedance lower than the thermal impedance of such material. Or partly with a conical chamber.
    The first gas inlet passage is typically at least partially provided with a cylindrical or conical chamber separated from the oxidizing gas inlet passage by a wall of aluminum or mullite material and having a thermal impedance less than that of the material.
    The manufactured baffle wall separates the reaction chamber into an exhaust gas outlet passage, the tubular fuel cell extends through the hole in the baffle wall to the exhaust gas outlet passage, and the hole in the baffle wall reacts with the flow of the partial reaction gas. It flows from the chamber into the exhaust gas outlet passage to combust with the partially reacting gas flying from the interior of the tubular fuel cell.
    Each tubular fuel cell is retained only at the end of the cell mounted within the manifold block.
    Each fuel cell may pass through a hole in the baffle wall, the partially reactive gas flowing away from the edge of the hole around the cell, and from the reaction chamber to the exhaust gas outlet passage, the It may also flow through the apertures through the spaces between the fuel cells.
    The first gas inlet passage has a plenum chamber below the manifold block, the fuel cell mounting end may extend through the manifold block, and the plenum chamber distributes the gas to the fuel cell mounting end. Let's do it.
    The first gas may be an oxidizing gas, and the power connecting means is connected to electrodes on the inside and outside of the fuel cell at ends disposed in the plenum chamber.
    The first gas inlet passage may have a thermally conductive gas conduit extending through the manifold block into the plenum chamber, the first length of the conduit for absorbing heat from the gas in the reaction chamber under normal operating conditions. Pass through the reaction chamber.
    The second length of the thermally conductive gas conduit may pass through at least a portion of the exhaust gas outlet passage.
    An annular chamber surrounds the reaction chamber, the annular chamber flowing from the annular chamber to the reaction chamber at the end of the annular chamber away from the gas inlet port means through which the gas flows through the annular chamber and the inlet port means. A gas outlet port means for gas, the gas outlet port means being located adjacent to the manifold block, the wall between the reaction chamber and the annular chamber being thermally conductive, for example aluminum or mullite or similar thermal impedance. It is formed of a material.
    One or more mixing ports may be provided in the wall between the annular chamber and the reaction chamber, the mixing port leading from the gas outlet port means to the chambers at the far end of the reaction chamber and the suction force generating means mixing from the reaction chamber to the annular chamber. The operation of the gas passing through the annular chamber to draw gas through the port creates a low pressure region of the annular chamber immediately adjacent to the mixing port.
    The fuel cell uses a zirconia-based electrolyte stabilized with yttrium oxide, mounted on glass ceramic (sold under the trade name Markor by Corning Glassworks), and the manifold block is made of ferritic stainless steel.
    Ignition means can be provided in the combustion zone to generate sufficient local heat to ignite the fuel gas in the presence of oxidizing gas.
    Control means causes the fuel gas to flow at a substantially higher rate than required for power generation at start-up to ignite the gas flow and to substantially increase the gas flow until a temperature of approximately 800 ° C. reaches the manifold block. It is also possible to control the flow of ignition means and fuel gas to maintain it at a speed.
    For commonly available SOFC components, the reaction temperature will be between 400 and 600 ° C. For standard reforming reactions with commonly used nickel catalysts, the reforming temperature will be between 600 and 800 ° C.
    In another aspect, the present invention consists of a space heater comprising a power generating device as described above, exhaust gas is used for space heating, and the generated power is distributed to other devices.
    In another aspect, the invention consists of a water heating cylinder incorporating a power generating device as described above, wherein the exhaust gas is used to heat the water supply of the water heating cylinder.
    In another aspect, the invention consists of a power generator as shown by the accompanying drawings and generally described herein by reference.
    For those skilled in the art to which this invention pertains, many modifications to the construction and broad embodiments and applications of the invention may be within the scope of the invention as defined in the appended claims. The description herein is illustrative and is not to be limited in any sense.
    Best Mode for Carrying Out the Invention
    Referring to FIG. 1, the plurality of tubular fuel cells 2 generate electricity as fuel passes through it and air passes along it. Batteries of this type are known in the art and presented by K Kendall and T. W. J. Longstaff at the 2nd European Solid Oxide Fuel Cell Forum (May 6-10, 1996) in Lucerne, Switzerland. Particularly suitable are the cells disclosed in the "SOFC joint power generation system" made of a 2 mm diameter extrusion tube. The cells are mounted on a base plate 5 which forms the top of the reforming chamber 7. The reforming chamber is provided with a reforming catalyst suitable for converting the carbon containing fuel into a mixture containing a large amount of hydrogen.
    Air enters the system through perforation rings 16, 17 mounted on the outside of the chamber, passes through the cell and burns with depleted fuel at the ends of the cell to exit the tube.
    The air withdraws heat from a heat exchange system comprising concentric pipes 4 and 6 to reach a predetermined operating temperature. Part of the heat is transferred to the reforming chamber 7.
    The inner tube 6 of the heat exchange system is an open end, and the outer tube 4 has a dead end blocked at one side. The four ends are arranged above the burners and the pipe is heated by passing fuel gas through the spaces between the pipes. When the outer tube is thermally insulated, most of the transferred heat passes through the inner tube.
    Start, stop and control of power generation units
    The system is started by opening the gas valve at ambient temperature and igniting the gas through the tubes. This starting operation can consist of a conventional ignition system mounted in an outer pipe. The gas flow can be 5 to 10 times the nominal gas flow required during electrical generation. Thus, a system with a rated power of 1 kW can be seen to introduce 10-20 kW of heat during startup. Such a system contains about 10 kg of stainless steel, so the heating operation to operating temperature should be less than one minute. When the temperature reaches about 800 ° C. as measured on the base plate, the start-up step is completed at this time.
    The system is then set to idle by adjusting the gas flow to a minimum that maintains the temperature of the system. This flow will be 10-30% of the nominal flow. As soon as the current passes (which can be detected by measuring the change in the magnetic field immediately), the gas flow is set sufficiently to allow the current to flow.
    The process temperature can be adjusted by introducing some air, mechanically controlling the resistance to air flow entering the system, and rotating the ring 17 relative to the ring 16, respectively.
    It is apparent that the above-described control operation can be performed by a conventional burner control system with some added functions.
    The above operation has a better advantage in terms of reliability and cost compared to a system capable of continuously changing the gas supply for the required current. The disadvantage is low system efficiency because most gases are burned at low power. Whether to use variable or fixed (or multiple fixed stage) gas flows depends on the purpose of use.
    In the stop phase, the gas must be supplied in an idle flow until the current is set to zero and reaches a temperature of about 300 ° C., below which the gas supply can be stopped.
    For example, too low a gas supply can lead to an erroneous situation where the voltage is too low resulting in oxidation of the anode. This situation must be detected by voltage measurement and braked so that the current is zero and the gas flow is idle.
    System dimensions
    The entire system has a diameter of about 40 cm (5 cm is also allowed for insulation) and a height of about 80 cm and accommodates about 800 cells each producing 1.5 W when operated under hydrogen. Thus, 1.2 kW of electrical energy is produced with an efficiency of 45% (LHV), whereby heat is generated at a temperature of 500 ° C. or higher and this heat can be recovered. The recovered heat can be used for other applications that require low calories such as space heating and water heating. In some cases, the heating performance of space or water is the main purpose, and power generation may be secondary.
    Tubular battery
    The battery 2 as shown in Figs. 1, 2 and 3 is composed of three layers. The layers typically have a diameter of 1 to 5 mm and a length of up to 500 mm. Larger systems may include cells up to 1000 mm in length. The outer layer, the cathode, is in contact with an oxygen containing gas such as air. Oxygen reacts with oxygen ions by picking up electrons in the layer. Oxygen ions move through the intermediate layer to become an electrolyte. This transfer occurs at temperatures between 600 and 1000 ° C. depending on the electrolyte material, which in turn determines the operating temperature. When oxygen ions arrive at the anode, which is an inner layer, the oxygen ions react with the fuel (eg, hydrogen) to form water. Hydrogen donates electrons that pass through the cathode through an electrical circuit.
    The anode is porous because the gas must be permeable and can be made of nickel mixed with the electrolyte. The electrolyte is an oxygen ion conductive material such as zirconia stabilized with yttrium oxide. The electrolyte must be dense enough to prevent gas components from passing through. The cathode forms an outer layer and can be made of a ceramic such as porous and doped LaMnO 3 .
    The electrolyte tube is made by preparing a paste of electrolyte material together with a binder and a plasticizer. The paste is extruded into a tube and then sintered.
    Anode and cathode materials comprising the slurry are prepared and disposed respectively inside and outside the electrolyte. The anode slurry is applied by suction and the cathode slurry is attached or sprayed. The electrodes are then sintered.
    Instead of using zirconia, other ion conductors can be used. Typical materials include, for example, doped Ce0 2 and doped perovskite.
    Still other electrodes are conductive ceramic oxide materials such as ceria (and other catalytic metals) and perovskite as anodes. As a cathode, LaCoO 2 is an example possible. The electrochemical activity of these materials is considered to be higher than the conventional electrode materials described above, especially at low temperatures.
    Another way to make cells is to extrude and sinter a tube of anode material first. A thin layer of electrolyte is applied to the tube and its contact area can be increased by applying suction to the anode tube as an anode. It is sintered, after which the cathode is applied and sintered.
    The advantage of this method is that thinner electrolytes are available, reduce internal resistance, thicker anodes can be used and increase the reforming capacity of the anode.
    Current pick up
    Electrons enter the cathode by passing through the connector 14 and an electrically conductive layer on the cathode. The connector 14 is arranged around the inlet end of a tubular cell made of, for example, nickel sheet.
    The electrically conductive layer (not shown) is, for example, silver wire or silver paste. Of course, any conductor with sufficient conductivity can be used.
    The connector 14 is made of sheet metal having a thickness of 0.2 to 0.3 mm, cut into a rectangle of about 8 8 mm and having a lip of about 3 8 mm. The connector is folded around the rod and has the same diameter as the tubular cell and is mounted on a ceramic tube. Small holes in the ribs provide connection to the anode wires of adjacent cells. The end of the lip is preferably leveled with the end of the cell to prevent short circuiting.
    The electrons produced at the anode are sent to a current collector made of, for example, nickel, which consists of a number of wires twisted together. By twisting the wires, electrical contact is ensured and there is also room for gas to pass through.
    Sealing
    Mounting each fuel cell in the manifold plate 5, which is generally a conductive material such as stainless steel, involves fitting the tubular fuel cell with the annular insulator. Sealing contact is preferred between the fuel cell and the insulator and between the insulator and the manifold plate 51. A manufacturing process has been developed to achieve the above object and this is described with reference to FIG.
    The ceramic ring 22 is temporarily glued to the ceramic insulator 13. Ceramic insulators are disposed around the cell and fitted around the connector 14. The ceramic insulator has a length of about 25 mm. The ring is about 4 mm long and fits around the ceramic tube. The ring is only half its length above the insulator, thus forming a small indentation 23 where the cement can be placed when the cell is placed. The cement is placed between the tubular cell and the insulator by applying suction to the other end of the insulator as a slurry. Thereafter, the indentation is filled with cement, so that a good seal is formed between the tubular battery 2 and the insulator 13.
    The battery assembly is bonded to the base plate in a manner similar to the above-described process of placing cement into the base plate and applying suction after placing the cell.
    To increase the contact area of the cement with the base plate, screws are tightened with standard size threads. Cements used are commercially available alumina, zirconia and magnesia cements.
    The material of the base plate may preferably be ferritic high grade stainless steel because the high grade stainless steel has a low coefficient of expansion and thus causes less inconsistency problems of expansion coefficients.
    Thus, the cells are connected in parallel in groups and the groups are connected in series and mounted on the base plate 5.
    In order to increase the number of cells per unit area and overall reliability, the cells can be bundled. This is shown in FIG. Multiple cells are disposed around the metal rod 29 to perform the function of current pickup. This assembly is bonded to the ceramic insulator and placed on the base plate similar to that seen in a single cell. The tubes are held against the rod by the wire 30.
    It is preferable that the ceramic insulator 13 and the manifold plate 5 are formed of a material having a coefficient of thermal expansion similar to that of the electrolyte material of the fuel cell so as to reduce the stress generated therebetween during heating or cooling. For fuel cells as described above, ceramic insulators made of glass ceramic materials such as machined glass ceramics sold under the trade name MACOR produced by Corning Glasswork, and alumina distribution layers using pack bonding techniques It has been found that a manifold plate formed of ferritic stainless steel coated with is suitable.
    burner
    At the top of the cell the small hollow ceramic tube 11 is hardened and the material may be alumina. The inner diameter is typically on the order of 0.5 mm so that the gas velocity is fast enough to keep the gas flame out of the tube.
    The system is made more resilient to external mechanical impact by placing a through plate having holes 24 coincident with the holes of the base plate at the end of the cell. This plate is held in place by the rod 26, which is screwed into the base plate. To prevent short circuiting, the holes are provided with an alumina tube 25 to harden on the burner plate. Small slots inside the alumina tube allow air to pass through. Thus, the tubular battery expands freely in the axial direction, but its movement in the radial direction is limited to prevent breakage caused by mechanical shock.
    Reforming chamber
    The base plate with cells and leads can be mounted to a pipe to form a chamber 7 and reformed therein, which allows the system to operate on reformed fuel mixtures such as natural gas or methane and steam. The reforming chamber is equipped with a reforming catalyst such as nickel wool. The reforming chamber to which the reformable fuel mixture is supplied is sufficiently heated by heat exchange from the exhaust gas to raise the temperature of the fuel mixture to a level sufficient to be reformed, such as 800 ° C. The reforming catalyst is ensured to be located in a sufficiently hot area of the chamber to prevent soot formation of the fuel. As a result, the catalyst 30 may be located on the through plate 31 mounted below several centimeters of the base plate 5. Alternatively, the catalyst may be disposed in the tube 2, in which case the reforming fuel mixture must reach the reforming temperature completely before entering the tube to ensure that soot formation or incomplete reforming on the tube surface does not occur. .
    Gas connection and electricity supply through it
    The positive and negative leads of the connected cell are electrically insulated and connected to the outside by a gas tight supply through the block. The component consists essentially of a longitudinal through bore steel rod 27 several centimeters long. Gas is supplied through the bore on the side of the rod and the wires 18, 19 pass through in a straight line. The wires bend obliquely after passing through the holes of the PTFE (or similar material) ring 20 at the bottom of the rod. A second PTFE (or similar material) plate 28 is located and a metal ring 21 is located. Metal and PTFE (or similar material) plates are screwed onto the steel rod to provide an airtight seal.
    Air flow control
    Oxygen (air) enters the system through the holes in the rings 16 and 17 and is located around the gas chamber. The inlet air extracts heat from the hot gas passing between the inner pipe 6 and the outer pipe 4 to transfer some of the heat to the fuel gas of the reforming chamber.
    To control the air supply, one of the rings 17 can rotate. By rotating the ring 17, some air is allowed into the system. Controlling the air supply is necessary to control the temperature of the flame, ie the process.
    system
    An electrochemical reactor providing electricity consists of a row of tubular fuel cells 2 mounted at one end on the base plate 5 and electrically connected.
    The base plate 5 functions as a manifold for fuel gas. Since only one end of the battery is retained, thermal stress is avoided. The base plate is mounted at one end of the pipe, and the interior thereof may include a reforming catalyst. The other end of the pipe is connected to the tube to carry the reformable fuel mixture to the system. Thus, the reforming chamber 7 is formed.
    Thus, fuel gas passes through the inside of the tube and air passes along the outside. Usually at temperatures of 600 to 1000 ° C., the gas is converted to provide electricity. Electricity is passed to one end of the cell through an electrically conductive wire or ink on the electrode. Typically, the cells will be electrically connected in series to the bottom (fuel side) of the base plate. The electrical connection between the cells is made on the fuel side of the base plate and the main electrical lead will have to pass through the wall containing the fuel. This consists of a feed through the block as described above.
    Fuel gas manifolded into the cell is typically converted from 50 to 90% as it passes through the cell. Thus, at the end of the tube, exhaustion of fuel will appear. Atmosphere 8 may access the system through convection through the holes in rings 16 and 17. By burning the depleted fuel, air is forced into the system and once it passes the cell, some of the oxygen is removed. Therefore, the burner is supplied with oxygen depleted air. The air also has the function of controlling the temperature of the system. Typically, the air flow should be 5 to 10 times greater than the flow of fuel to prevent excessive temperature differences along the length of the cell.
    A heat exchange system consisting of two coaxially arranged pipes transfers the heat generated by the burners and carries it back to the system inlet. The outer pipe 4 has one closed end and the inner pipe 6 has two open ends. The inner pipe extends from near the bottom of the reforming chamber to the end of the tube. As a result of the combustion process, air is forced between the reforming chamber and the inner pipe. Air passes through the cells and some of the oxygen is converted through an electrochemical process. This oxygen partially depleted is burned with the depleted fuel gas. Due to the blocked end of the outer tube, the final heat cannot rise and then descend along the outside of the inner pipe, which transfers heat to the inner pipe and consequently to heat into the inlet air.
    Alternative system of Figure 5
    A system believed to provide better performance than the system described above is shown in FIG. This embodiment comprises a reaction chamber 40 and a combustion chamber in a thermally conductive wall 48 surrounded by an annular space 46 which serves as an inlet passage for one of the reaction gases (of the embodiment shown as fuel gas). Including (41) provides potentially good heat exchange.
    More specifically, the device comprises a reaction chamber 40 bounded by its thermally conductive wall 48 around its side and may be, for example, alumina or mullite, and a manifold block 51 at the lower end of the reaction chamber. And a baffle plate 47 that defines an upper end of the reaction chamber. By having the embodiment of FIG. 1, the fuel cell 61 is mounted at one end 62 of the manifold block 51, respectively. The fuel cell 61 extends vertically through the opening 63 of the baffle plate 47 and the reaction chamber 40. The opening 63 has a larger diameter than the tubular fuel cell 61, which provides an annular spacing around orthogonal fuel cells. The ends 65 of the fuel cell 61 extend past the baffle 47 into the combustion chamber 41 which forms part of the outlet passageway for the exhaust gas. It can be seen in FIG. 5 that only a few fuel cells are shown to ensure the accuracy of the drawing. Hundreds of fuel cells can be provided in very large systems.
    The combustion chamber 41 is bounded by a baffle plate 47 with a lower boundary and delimited by a thermally conductive wall 48 and a conical extension 64, in which a substantial part of the periphery and upper region form a roof. All. The combustion chamber 41 has an outlet 43 therefrom. The gas inlet pipe 49 extends through the exhaust outlet 43 and extends downward through the combustion chamber 41, extends through the opening 50 of the baffle plate 47, the reaction chamber 40 and the manifold. It extends through the fold block 51. The exhaust outlet 43 is shown in cut form in FIG. 5, but for improved heat exchange between the exhaust gas and the inlet pipe 49, the exhaust outlet 43 and the inner pipe 49 are spaced larger than necessary. It is made of coaxial shape.
    The inlet pipe 49 extends into or through the manifold block 51 to have an outlet in the plenum chamber 42 below the manifold block 51. The plenum chamber 42 is surrounded by the lower plate 52 and its sides are surrounded by the outer wall 57.
    The lower edge 60 of the thermally conductive wall 48 is located on the manifold block 51 by an annular step 59 formed therein. The outer wall 57 is coaxial with and spaced apart from the thermally conductive wall 48 to form an annular chamber 46 surrounding the reaction chamber 40 and the combustion chamber 41. The outer wall 57 is sealed against the periphery of the lower plate 52 and the manifold block 51. The wall 57 may be provided with a stainless steel sheet, for example, and the outer wall of the device may preferably be provided with an insulating layer 58 around its outer side.
    The annular chamber 46 provides the main part of the inlet passage for the second reactant gas entering through the inlet 45 proximate the exhaust outlet 43. The annular chamber 46 has one or more outlet ports 54 at its lower end adjacent to the manifold block 51. To help raise the inlet gas to the required temperature, heat exchange is provided by recycling a small amount of gas from the reaction chamber out through the outlet port 55 and back to the annular passage 46. To aid in the intake of gas passing through the outlet port 55, the inclined flange 56 is provided adjacent to the port, such as a venturi tube, to create a low pressure region immediately adjacent to each port 55. May be
    In addition, the recycled and depleted fuel gas allows a partial oxidation reforming reaction to be used, so that water does not have to be present in the fuel gas vapor.
    In the embodiment of the invention shown in FIG. 5, the inlet passage can be used for oxidizing gas or fuel gas with a reforming catalyst appropriately located at the lower end of the annular chamber 46 or in the plenum chamber 42. I think. The operation of this embodiment is described with fuel gas entering at inlet 45 and traveling through annular chamber 46 and oxidizing gas entering at inlet 44 of inlet tube 49 and distributed through the plenum chamber. It is shown that the reforming catalyst 65 is located below the annular chamber 46.
    In operation of the apparatus, fuel gas is supplied at the inlet 45 as indicated by arrow 71. The supply of fuel gas is preferably controlled by the system controller to regulate the fuel gas pressure using conventional means. The oxidizing gas is supplied as indicated by arrow 70 at the inlet 44 of the inlet tube 49. In addition, the supply of oxidizing gas may be controlled by variably limiting a system controller, such as an inlet pipe. Under certain conditions, prepressurization of the oxidizing gas may be necessary, for example achieved by a small fan.
    The fuel gas travels in the passage indicated by arrow 72 over the thermally conductive roof 64 of the combustion chamber 41 and into the annular chamber 46 surrounding the thermally conductive wall 48. The fuel gas is heated by passing over the thermally conductive wall heated by the combustion of the combustion chamber 41 and the hot gas of the reaction chamber 40 and heated by the exothermic fuel conversion process.
    The inlet combustion gas is further heated by mixing the reaction chamber with a small amount of depleted fuel gas exiting through the outlet port 55 as indicated by arrow 82. Thus, the fuel gas is raised to a temperature of approximately 800 ° C. before reaching the reforming reformate that is reformed as the gas flows during steady state of the apparatus.
    The reformed fuel gas then flows through the port 54 into the reaction chamber in the manner indicated by arrow 73. The reformed fuel gas passes upwards through the reaction chamber, passes over the outside of the fuel cell, exits the reaction chamber through the outlet port 55 and back out into the annular chamber 56, or the opening 63 and the baffle plate Exit through the gap provided between 47 and through the passing fuel cell 61. The fuel gas exits into the combustion chamber 41 via an annular gap provided between the opening 50 and the inlet pipe 49 if such a gap is present. The presence of this gap depends on the material selected for the inlet pipe 49 and the baffle plate 47 and depends on whether or not they are fitted with tight tolerances by the coefficient of thermal expansion.
    The oxidizing gas enters through the inlet 44 of the inlet pipe 49 as indicated by arrow 70 and passes downwardly from its end to the outlet 66 through the inlet pipe as indicated by arrow 74, Go out into chamber 42 and disperse therein as indicated by arrow 76. The plenum chamber supplies almost uniform air to the end 62 of the fuel cell 61 that is open therein. The oxidizing gas passes into the open end 62 of the fuel cell 61 as indicated by arrow 77 so as to pass through it as indicated by arrow 78.
    In the embodiment shown in FIG. 5, the anode and cathode of the fuel cell are reversed by comparing with the embodiment shown in FIG. The cathode is formed on the inner surface of the electrolyte tube and the anode is formed on the outer surface of the electrolyte tube. The oxidizing gas passing upwards of the inside of the tube and the fuel gas around the outside of the tube react as described above to create a potential between the inner and outer electrically conductive layers of the fuel cell. The electrical connection to the electrically conductive layer is preferably formed at the lower end 62 of the cell 61 of the normal use plenum chamber 42 which contains no heated gases and contains only heated air, which is an appropriately open environment. .
    The depleted oxidizing gas passes out of the upper end 65 of the fuel cell 61 into the combustion chamber 41 and, for example, with the depleted fuel gas having the depleted fuel gas passing through the opening 83 as indicated by arrow 90. 81). Combustion provides extra heat in the conductive wall 64 and inlet tube 49 and thus provides extra heat to the combustion and oxidizing gases introduced into the system. The exhausted and combusted exhaust gas then passes out of the apparatus via exhaust outlet 43.
    While the configuration of FIG. 5 has a greater chance of heat transfer than the system of FIG. 1 having a combustion chamber, a heat providing area and a reaction chamber 40 contained within the fuel gas inlet chamber 46, the oxidizing gas inlet pipe has an exhaust outlet 43. It is evident that the excess heat is extracted from the exhaust gas at. The system also provides an electrical connection to the fuel cell to be the calm region of the device in the air plenum chamber under the manifold plate 51. From an assembly point of view, the device is relatively simple to consist of thermally conductive walls 48, 64, manifold plates 51, and outer shells 57, 58 that are positioned and fixed across the base plate 52. A relatively simple ceramic ring seal is sufficient to seal this connection. Thermally conductive walls 48 and 64 are easily located across the stepped portion 59 of the manifold plate 51 and hold the baffle plate 47 in place. The manifold plate 51 having the fuel cell 61 and the inlet tube 49 may be preassembled in effect as already described.
    Advantages over the prior art
    The above designs overcome several problems associated with a flat fuel cell design for the following reasons.
    The interconnection of the flat design constitutes 80% to 90% of the volume of the stack but does not directly contribute to power generation.
    When using metal, the interconnects have a higher coefficient of thermal expansion than the ceramic material of the cell. This causes rupture of the ceramic. As a result, heating to the process temperature should be done slowly. This takes at least six hours, which is difficult to implement.
    The problem of sealing appears to be difficult to overcome in planar design, and repeated starting and stopping worsens the sealing.
    Sealing and contact resistance requirements require a holding force of approximately 100 N / cm 2. At the required operating temperature, this stress causes creep problems.
    To apply retention, a large body and other components are required.
    The newly developed design overcomes most of these problems because the cells are free to expand because they are retained only at one end. In addition, the entire system is integrated into one device, the main features of which are as follows.
    Air supply does not require a gas blower or pump, but natural convection is used to remove the air.
    The required process temperature is reached and maintained by transferring heat from the burned excess fuel to the air inlet.
    The current state of the art in fuel cells requires that the fuel has a high amount of hydrogen and a relatively small amount of hydrocarbons. At the electrode surface, the kinetic conversion of the gas to hydrogen is not sufficiently active, thus requiring a prior reforming step. In this design, the reforming catalyst is located in the fuel chamber below the fuel cell together with the reforming fuel mixture previously heated by the exhaust gas.
    In this way, a large portion, commonly referred to as the "balance of plant", is integrated into the fuel cell stack. This can significantly reduce the cost of the system as a whole.
    权利要求:
    Claims (17)
    [1" claim-type="Currently amended] An apparatus for generating power,
    A plurality of tubular solid oxide fuel cells disposed in the reaction chamber, each having an inward reaction surface and an outward reaction surface, and electrodes coupled with the respective surfaces, one end of which is mounted in a manifold block;
    A first gas inlet passage for supplying a first gas passing along the exterior of the fuel cell to the reaction chamber;
    A second gas inlet passage for supplying a second gas to the mounting end of the fuel cell so as to pass along the interior of the fuel cell;
    Unreacted gases can be internally combusted and an exhaust gas outlet passage from the reaction chamber adjacent the ends of a fuel cell located away from the manifold block for delivering exhaust gas to the outlet,
    Power collection means for connecting a conductor on the interior and exterior of the fuel cell;
    Equipped;
    One of the first and second gases is a reforming fuel gas, the other is an oxidizing gas, and the gas passages carry one of the reformable gas or the oxidizing gas, respectively, according to the placement of the reaction surface of the fuel cell,
    The reformable gas delivery passage has a reforming catalyst therein and is disposed in heat transfer relationship with the exhaust gas passage and the reaction chamber such that during steady state operation the temperature rises to the temperature of the catalyst where the internal gases can be reformed,
    The oxidizing gas delivery passage is arranged in a heat transfer relationship with the exhaust gas passage and the reaction chamber such that during steady state operation internal gases rise to the fuel cell reaction temperature at which the fuel cell operates.
    Power generating device, characterized in that.
    [2" claim-type="Currently amended] The baffle wall of claim 1, wherein a baffle wall separates the reaction chamber from the exhaust gas outlet passage, the tubular fuel cell extends through the hole in the baffle wall to the exhaust gas outlet passage, and the hole in the baffle wall is And a flow of the partially reacting gas from the reaction chamber to the exhaust gas outlet passage to cause combustion with the partially reacting gas flowing from the interior of the tubular fuel cell.
    [3" claim-type="Currently amended] 2. The power generation device of claim 1, wherein each tubular fuel cell is retained only at an end mounted in the manifold block.
    [4" claim-type="Currently amended] 3. The partially reactive fuel cell of claim 2, wherein each tubular fuel cell is retained only at an end mounted in the manifold block and passes through the aperture in the baffle wall and flows partially from the reaction chamber to the exhaust gas outlet passage. And a gas flows through the hole through a space between the wall and each fuel cell.
    [5" claim-type="Currently amended] The fuel cell mounting end of claim 1, wherein the first gas inlet passage includes a plenum chamber below the manifold block, the fuel cell mounting end distributing the gases to the fuel cell mounting end. Extend through the manifold block and the plenum chamber.
    [6" claim-type="Currently amended] 6. The power generation device of claim 5, wherein the first gas is an oxidizing gas and the power connection means is connected to electrodes inside and outside the fuel cell at ends disposed in the plenum chamber.
    [7" claim-type="Currently amended] 6. The method of claim 5, wherein the first gas inlet passage has a thermally conductive gas conduit extending through the manifold block into the plenum chamber and wherein the first gas inlet passage is adapted to absorb heat from the gas in the reaction chamber under steady state operation. 1 wherein the length of the gas inlet passage passes through the reaction chamber.
    [8" claim-type="Currently amended] 8. The apparatus of claim 7, wherein said thermally conductive gas conduit has a second length through at least a portion of said exhaust gas outlet passageway.
    [9" claim-type="Currently amended] 9. The annular chamber of claim 1, wherein the second gas inlet passage comprises an annular chamber surrounding the reaction chamber, gas inlet port means leading to the annular chamber, and the annular chamber from the inlet port means. A gas outlet port means extending from said annular chamber to said reaction chamber and located adjacent said manifold block at a distal end of said wall, wherein a wall between said reaction chamber and said annular chamber is thermally conductive.
    [10" claim-type="Currently amended] 10. The apparatus of claim 9, further comprising at least one mixing port in a wall between the reaction chamber and the annular chamber, wherein the mixing port extends from the gas outlet port means to a distant end of the reaction chamber between the reaction chamber and the annular chamber. And the mixing port includes suction force generating means for generating a low pressure region in the annular chamber immediately adjacent to the mixing port by passing the gas to suck gas passing from the reaction chamber into the annular chamber. Power generating device.
    [11" claim-type="Currently amended] 11. A fuel cell according to any one of claims 1 to 10, wherein the mounting end of each fuel cell has a mounting end mounted inside a tubular ceramic insulator having a thermal expansion coefficient similar to that of the fuel cell, wherein the ceramic insulator is And a power generating device bonded in a hole passing through the manifold block made of a material having a coefficient of thermal expansion similar to that of an insulator.
    [12" claim-type="Currently amended] 12. The power generator according to claim 11, wherein the fuel cell uses a zirconia-based electrolyte stabilized with yttrium, the insulator is glass ceramic, and the manifold block is ferritic stainless steel.
    [13" claim-type="Currently amended] 13. The electric power according to any one of claims 1 to 12, comprising ignition means in the combustion zone capable of generating local heat sufficient to ignite the fuel gas in the presence of the oxidizing gas. Generating device.
    [14" claim-type="Currently amended] 14. The system of claim 13, further comprising a system control means for controlling the flow of said ignition means and at least said fuel gas, said system control means allowing said fuel gas to flow at a substantially higher rate than required for power generation at start-up. And ignite the gas flow and maintain the gas flow at the speed until a temperature of approximately 800 ° C. reaches the manifold block.
    [15" claim-type="Currently amended] A space heater comprising the power generator according to any one of claims 1 to 14,
    Space heater, wherein the generated power is distributed to other devices.
    [16" claim-type="Currently amended] A power generating device shown in FIG. 1 and substantially described herein with reference to FIG. 1.
    [17" claim-type="Currently amended] A power generating device shown in FIG. 5 and substantially described herein with reference to FIG. 5.
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    同族专利:
    公开号 | 公开日
    BR9812715A|2000-08-22|
    NZ503606A|2002-05-31|
    CA2316381A1|1999-04-08|
    JP2001518688A|2001-10-16|
    AU9369698A|1999-04-23|
    EP1032954A1|2000-09-06|
    EP1032954A4|2004-06-02|
    WO1999017390A1|1999-04-08|
    AU730602B2|2001-03-08|
    US6492050B1|2002-12-10|
    IL135330A|2004-05-12|
    IL135330D0|2001-05-20|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    法律状态:
    1997-10-01|Priority to NZ328885
    1997-10-01|Priority to NZ32888597
    1998-10-01|Application filed by 조나단 알. 우드, 아쿠멘트릭스 코포레이션
    1998-10-01|Priority to PCT/NZ1998/000151
    2001-04-16|Publication of KR20010030874A
    优先权:
    申请号 | 申请日 | 专利标题
    NZ328885|1997-10-01|
    NZ32888597|1997-10-01|
    PCT/NZ1998/000151|WO1999017390A1|1997-10-01|1998-10-01|Integrated solid oxide fuel cell and reformer|
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