![]() PEM fuel cell
专利摘要:
The invention relates to a device for conditioning at least one process gas (1, 2), which is supplied via at least one process gas feed (6, 7) to at least one electrochemical converter, in particular a fuel cell (3). The process gas supply (6, 7) has a moistening unit (8, 9) with which a moistening agent (4, 5) can be introduced into the process gas (1, 2). As moistening agent (4, 5) water in the supercritical state in the process gas (1,2) can be introduced. 公开号:AT519349A4 申请号:T51197/2016 申请日:2016-12-30 公开日:2018-06-15 发明作者:Kancsár János;Ing Christoph Kügele Dipl;Dr Jakubek Stefan 申请人:Avl List Gmbh; IPC主号:
专利说明:
Summary The invention relates to a device for conditioning at least one process gas (1, 2) which is fed to at least one electrochemical converter, in particular a fuel cell (3), via at least one process gas supply (6, 7). The process gas supply (6, 7) has a humidification unit (8, 9) with which a humidifier (4, 5) can be introduced into the process gas (1, 2). Water in the supercritical state can be introduced into the process gas (1, 2) as the humidifying agent (4, 5). Fig. 1 -ιοί / 13 AV-3887 AT PEM-B fuel cell The invention relates to a method for conditioning at least one process gas, which is fed to at least one electrochemical converter, in particular a fuel cell, the process gas being moistened with a humidifier. Furthermore, the invention relates to a device for conditioning at least one process gas, which is supplied via at least one process gas supply to at least one electrochemical converter, in particular a fuel cell, the at least one process gas supply having a humidification unit with which a humidifier can be introduced into the process gas. The invention further relates to an energy conversion unit for generating electrical energy from a first hydrogen-containing process gas and a second oxygen-containing process gas in at least one fuel cell, the first process gas being supplied to the at least one fuel cell via a first process gas supply and the second process gas via a second process gas supply. To ensure the functionality, performance and durability of fuel cells, especially low-temperature PEM fuel cells (LT PEMFC), the process gases (hydrogen and air) must be conditioned. In addition to the temperature, pressure and mass flow, the humidity is also set depending on the operating point. The Moisture plays a decisive role here, since only a water-containing membrane is used for Hydrogen cations is permeable. To be particularly efficient, high levels of moisture are required. However, water drops in the gas can block the fine gas channels in the fuel cell, which leads to an undersupply of reactants and thus to a reversible and irreversible loss of performance (the latter also called degradation). Furthermore, the membrane swells when water is absorbed; when it is released, this process is reversed, which is associated with mechanical stress. Due to the strongly changed relative humidity of the process gases, cyclical swelling and swelling of the membrane can damage it and cause irreversible performance losses and thus degradation. Depending on the application - in operation (in a fuel cell system) or on a test stand - there are different methods for moistening the reactants. In a fuel cell system, gas-gas membrane humidifiers with sulfonated tetrafluoroethylene polymer are mostly used. The exhaust gas from the fuel cell is led past the process gas separately through a Teflon membrane. The temperature and humidity of the two gases are adjusted via the membrane. This procedure shows a slow An2 / 13 1 AV-3887 AT Talk time and poor controllability and is therefore not suitable for use in a test bench, for example. Another method, which is mainly used on stationary research test benches, makes use of a so-called “bubbier”. The gas is blown from below through a container with water to humidify the gas. This method is particularly suitable for creating very constant humidity conditions, but dynamic changes are hardly possible. Other processes with better responsiveness and better controllability, which are mostly used for test benches, are direct evaporation, water injection and the direct introduction of water vapor. In the former, water is sprayed onto a heated plate using a mass flow controller. The water evaporates and is then added to the process gas. The good meterability of the water is advantageous here, since it is added in liquid form. However, the heating plate is sluggish and has to be heated to a greater or lesser extent, depending on the amount of water. If the amount of water is increased too quickly, the plate can cool down too much and the water begins to collect in the chamber. There is also a dead time between water injection and steam supply to the process gas, since the liquid water first has to be evaporated. During water injection, water is atomized as finely as possible via a one- or two-component nozzle and fed directly to the process gas. The good meterability is again advantageous, but the evaporation enthalpy must be taken from the process gas itself. That the gas must be overheated to carry enough heat at high relative humidity. In addition, the particle evaporation depends on the ratio of the saturation partial pressure on the particle surface and the water vapor partial pressure in the gas. With Equilibrium, evaporation stops. The formation of water drops can not be avoided or can only be avoided with great difficulty. In another approach, water vapor is generated in a boiler and this is then added to the process gas via valves. The high dynamics and short response time are advantageous, but the water vapor can only be dosed with difficulty. Variants of the previously described methods are also known. However, especially in dynamic operating conditions, all of these methods have disadvantages, with the formation of water drops or poor control quality (overshoot or undershoot) of the moisture which can lead to unfavorable or damaging operating conditions for the fuel cell. It is the object of the present invention to overcome these and other disadvantages of the prior art. / 13 2 ' AV-3887 AT According to the invention, the object is achieved by a method of the type mentioned at the outset, in which water in the supercritical state is used as the moistening agent. With this method, the relative humidity of the process gases can be set with high control quality and a fast response time. The method can be used for all electrochemical converters that require the humidification of process gases, whereby the formation of droplets should be avoided. The invention is particularly advantageous for fuel cells, such as of the PEMFC, DMFC, PAFC, AFC, DMFC, SOFC or similar type. The method according to the invention is particularly suitable for fuel cells of the low temperature polymer electrolyte membrane fuel cell (LT PEMFC) type. In a preferred embodiment, the supercritical water introduced as a humidifier into the process gas can have a specific enthalpy of over 2800 kJ / kg. With an isenthalpic expansion, no liquid water is formed, since the corresponding isenthalpics run completely outside the wet steam area. Advantageously, the humidifier can be introduced into a process gas supply via at least one humidification unit with an essentially isenthalpic throttle, which can optionally be designed as an injector. This enables a fast and precisely controllable injection, the amount of the humidifier introduced via the throttle being able to be determined and controlled very precisely using a mass flow controller. In connection with the present description, a “restriction” is generally used to denote a cross-sectional constriction in a flow channel. The throttle can be designed, for example, as an orifice, nozzle or injector. A aperture is a hole with a non-rounded entrance and a generally conical exit. A nozzle has a changing cross-section over the course of the flow, and an injector is a throttle, orifice or nozzle which is designed to be closable and whose cross-section can be adjusted if necessary. The device mentioned at the outset for conditioning at least one process gas achieves the object according to the invention in that water can be introduced into the process gas in the supercritical state as the humidifying agent. The water can, for example, be allowed to flow in continuously via a throttle, and the amount of water flowing in can be regulated via the pressure. The humidification unit can advantageously have an injector which opens into the process gas supply. This enables the injection quantity to be metered precisely. The metering can be implemented in a similar manner to that of internal combustion engines with a common rail system. The injection quantity can be metered, for example, by opening and closing times intermittent with an opening frequency. At / 13 3 ' AV-3887 AT nevertheless to ensure a constant supply of humidifier, several injectors, which each open into the same process gas supply, can also be provided. The control can take place at different times so that the same amount of humidifier flows in continuously. The energy conversion unit according to the invention has a device described above. A plurality of fuel cells can advantageously be arranged in at least one cell block in the energy conversion unit, wherein the first process gas supply and / or the second process gas supply can be assigned to a plurality of fuel cells of the cell block. The present invention is explained in more detail below with reference to FIGS. 1 to 3, which show exemplary, schematic and non-limiting advantageous embodiments of the invention. It shows 1 shows a schematic representation of a fuel cell with a device according to the invention; FIG. 2 shows a schematic representation of a cell block 11 provided with the device according to the invention, consisting of several stacked fuel cells, and FIG. 3 shows a T-s diagram for water. With reference to FIG. 1, the properties and structure of a fuel cell 3 are described on the one hand in general and on the other hand specifically in connection with the present invention. The fuel cell 3 shown schematically in FIG. 1 is a PEM fuel cell (English: “Polymer Electrolyte Membrane Fuel Cell - PEMFC”), which is also referred to as “Solid Polymer Fuel Cell - SPFC” or “Polymer Electrolyte Fuel Cell - PEFC” , Depending on the electrolyte used, the fuel cell 3 operates in the temperature range from room temperature to about 80 ° C, with short-term temperature peaks of up to 95 ° C being possible (low-temperature PEMFC or LT-PEMFC) or 130 to 200 ° C (high-temperature PEMFC) or HT-PEMFC). Between HT-PEMFC and LT-PEMFC there is also MT-PEMFC (medium temperature PEMFC). This works in temperature ranges from around 100 ° C - 130 ° C. However, the transitions between these types of fuel cells are fluid, so that a clear demarcation is not always possible. The fuel cell 3 essentially consists of a central proton-conducting membrane 12, on the first side surface (this is the hydrogen side - shown on the left in FIG. 1) an anode 13 is arranged, and on the opposite second side surface a cathode 14 is arranged. -45/13 AV-3887 AT On the anode 13 side, a first process gas 1 is supplied to the anode 13 via a first distribution unit 17 and a first gas diffusion layer 15 via a first process gas supply 6. The first process gas 1 (educt) is, for example, hydrogen or a hydrogen-containing gas. Hydrocarbon compounds (ethanol, methanol, methane / natural gas, etc.) can also be added. This requires an internal (in the fuel cell) or external (as a separate unit) reforming of the hydrocarbon. On the side of the cathode 14, a second process gas 2 is supplied to the cathode 14 via a second process gas supply 7 via a second distribution unit 18 and a second gas diffusion layer 16. The second process gas 2 is or contains oxygen. The second process gas 2 can e.g. Air can be used. In order to humidify the first process gas 1, a first humidification unit 8 is provided on the first process gas supply 6, via which a first humidifier 4 can be metered into the stream of the first process gas 1. Likewise, a second humidification unit 9 is provided for humidifying the second process gas 2 on the second process gas feed 7, via which a humidifier 5 can be introduced in a metered manner into the stream of the first process gas 1. According to the invention, supercritical water is used as the first humidifier 4 and / or second humidifier 5, which can be provided to the humidification units 8, 9 by at least one water treatment unit 24. The water treatment unit 24 brings water to a supercritical state and makes it available to the humidification units 8, 9. High-purity water is preferably used in order to avoid that contaminants damage the fuel cell or the water treatment unit. The amount of supercritical water emitted by the humidification units 8, 9 can be determined by means of measuring devices 26, 26 '. As an alternative to this central water treatment, the water can also be brought to a supercritical state decentrally for each humidification unit. The humidifier flows through a throttle 27, 27 'into the respective process gas supply 7, 8, the shape of the throttle 27, 27' being able to be optimized as required, for example in the form of an orifice, nozzle or as an injector. The inflow process via the throttle 27, 27 'can be described as essentially isenthalpic. The unit consisting of proton-conducting membrane 12, first gas diffusion layer 15, second gas diffusion layer 16, first distribution unit 17 and second distribution unit 18 is referred to in the context of the present disclosure as a fuel cell 3. As is clear to the skilled person, a plurality of fuel cells can be summarized 3 to a cell block 11, wherein a cell block 11 from a plurality of fuel cells 3 gemein6 / 13 5 ' AV-3887 AT can have the same first process gas supply 6 and a common second process gas supply 7. Such a cell block 11 consisting of several fuel cells 3 is shown schematically in FIG. 2. The respective distribution units 17, 18 between two adjacent 5 fuel cells 3 are designed in a manner known per se as bipolar plates 19 which have flow grooves on both sides, in which the respective process gas 1, 2 is directed to the gas diffusion layers 15, 16 arranged next to it. Coolant channels may still run in the bipolar plates 19, but these are not shown in FIG. 2 for the sake of clarity. The first process gas 1 is introduced into the flow grooves 20 running from top to bottom in FIG. 2, the second process gas 2 is introduced into the flow grooves 21 running horizontally in FIG Side. The unit consisting of cell block 11 with the process gas feeds 6, 7 and humidification units 8, 9 provided thereon forms an energy conversion unit 10. The first and second humidifying means 4, 5 are injected by the two humidifying units 8, 9 according to the invention into supercritical water into the flow of the respective process gas. The throttles of the moistening units 8, 9 are designed as injectors 22, 23, as a result of which the amount of moistening agent 5 introduced can be quickly regulated and scaled. When humidifying process gases 1,2, the following conditions must be taken into account in general: • Liquids are easier to dose than gases. • During the phase transition from the liquid to the gaseous state, called evaporation, energy is taken from the environment (endothermic reaction). • The enthalpy of vaporization is a function of temperature and decreases with increasing temperature. • At the critical point, the enthalpy of vaporization = 0. • Evaporation can take place through boiling or evaporation. · Evaporation of a liquid takes place when the temperature-dependent saturation vapor pressure of the substance in the surrounding gas is higher than the current partial pressure of this substance in the gas. • Boiling takes place when the temperature-dependent saturation vapor pressure of the liquid is higher than the pressure of the surrounding gas phase. -67/13 AV-3887 AT • In the wet steam area, liquid and gaseous water coexist. In the process in question, supercritical water (English: Super Critical Water - SCW) is added to the process gases of the fuel cell directly via an injector 22, 23. This changes directly (i.e. without an enthalpy change being necessary) into the gaseous state without liquid water, e.g. in the form of water droplets. Two circumstances are used here: First, the density of supercritical water can be easily determined, so that the meterability of supercritical water is comparable to the meterability of liquid water. The density of supercritical water is roughly between that of liquid and gaseous water.Therefore, methods such as the mass flow-determining Coriolis principle can be used for measurement, which achieve better measurement results with higher media density and therefore benefit from the higher density pull. Secondly, the enthalpy increase for the evaporation of the water is already inside Supercritical water energy stored. In the isenthalpic expansion of the supercritical water into the process gas, this goes directly into the gas phase, the area of wet steam is avoided. This isenthalpic relaxation is shown in Figure 3, which shows a T-s plot of water. Starting from a supercritical state of the water (SCW), the Ent20 tension runs along an isenthalpic 25. At an enthalpy of about 2800 kJ / kg, this isenthalpic 25 runs completely outside the wet steam area, so that during the relaxation of the water, i.e. forms no liquid water at the transition from the supercritical to the gaseous state of matter. The supercritical state is generally the area of the water above the critical one Point (which is located in the T-s diagram at the top vertex of the wet steam area). According to the general definition, water is in the supercritical state if it has a temperature of over 647 K and a pressure of over 22.1 MPa. The injection quantity can be controlled in a conventional manner. For example, the injection quantity can be controlled on a map basis, with linear controllers and / or via non-linear model-based control approaches. / 13 7 ' AV-3887 AT Reference numerals: first process gas 1 second process gas 2 fuel cell 3 first humidifier 4 second humidifier 5 first process gas supply 6 second process gas supply 7 first humidification unit 8 second humidification unit 9 energy conversion unit 10 cell block 11 proton-conducting membrane 12 anode 13 Cathode 14 first gas diffusion layer 15 second gas diffusion layer 16 first distribution unit 17 second distribution unit 18 Bipolar plate 19 Flow groove 20, 21 injector 22, 23 Water treatment unit 24 Isenthalpe 25 Measuring device 26, 26 ' Throttle 27, 27 '/ 13 8 ' AV-3887 AT
权利要求:
Claims (2) [1] 1.3 11/13 AVL List GmbH 1. Method for conditioning at least one process gas (1, 2) which is fed to at least one electrochemical converter, in particular a fuel cell (3), the process gas (1, 2) being humidified with a humidifier (4, 5), 5 characterized in that water in the supercritical state is used as the humidifying agent (4, 5). 2. The method according to claim 1, characterized in that the supercritical water introduced as a humidifying agent (4, 5) into the process gas (1, 2) has a specific enthalpy of over 2800 kJ / kg. 10 3. The method according to claim 1 or 2, characterized in that the moistening agent (4,5) via at least one moistening unit (8, 9) with an essentially isenthalpic throttle (27, 27 '), optionally as an injector (22, 23 ) is formed, is introduced into a process gas supply (6,7). 4. Device for conditioning at least one process gas (1, 2) which 15 via at least one process gas supply (6, 7) at least one electrochemical one Transducer, in particular a fuel cell (3), is led, the at least one process gas supply (6, 7) having a humidification unit (8, 9) with which a humidifier (4, 5) can be introduced into the process gas (1,2) is characterized in that water as a humidifier (4, 5) in the supercritical state in the process gas 20 (1,2) can be introduced. 5. The device according to claim 4, characterized in that the humidification unit (8,9) has an injector opening into the process gas supply (6, 7). 6. Energy conversion unit (10) for generating electrical energy from a hydrogen-containing first process gas (1) and an oxygen-containing second process gas 25 (2) in at least one fuel cell (3), wherein the first process gas (1) via a first Process gas supply (6) and the second process gas (2) via a second process gas supply (7) of the at least one fuel cell (3), characterized in that the energy conversion unit (10) has a device according to one of claims 4 or 5. 30 7. Energy conversion unit (10) according to claim 6, characterized in that a plurality of fuel cells (3) in at least one cell block (11) is arranged, wherein in each case the first process gas supply (6) and / or the second process gas supply (7) one A large number of fuel cells (3) of the cell block (11) are assigned. -910 / 13 AVL List GmbH [2] 2.3
类似技术:
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同族专利:
公开号 | 公开日 AT519349B1|2018-06-15| CN110114921A|2019-08-09| WO2018121957A1|2018-07-05| CA3048938A1|2018-07-05| JP2020516010A|2020-05-28| DE112017006675A5|2019-12-12| KR20190099063A|2019-08-23|
引用文献:
公开号 | 申请日 | 公开日 | 申请人 | 专利标题 EP2639869A1|2010-11-12|2013-09-18|Panasonic Corporation|Method for operating solid polymer fuel cell system, and solid polymer fuel cell system| US20130022883A1|2011-07-18|2013-01-24|Hyundai Motor Company|Apparatus and method for activating fuel cell stack| WO2016001938A1|2014-07-03|2016-01-07|Council Of Scientific And Industrial Research|Internal humidification in low temperature pem fuel cell by means of a wick| US4581105A|1984-06-20|1986-04-08|The Dow Chemical Company|Electrochemical cell operating near the critical point of water| JP2002216820A|2001-01-15|2002-08-02|Eco Design Kk|Fuel cell by supercritical hydroxilation reaction| DE10162202B4|2001-12-18|2007-12-27|Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V.|Hydrocarbon reformer| US8038743B1|2002-11-27|2011-10-18|Drs Sustainment Systems, Inc.|Systems and methods for supercritical water reformation of fuels and generation of hydrogen using supercritical water| KR101575416B1|2013-11-29|2015-12-21|현대자동차주식회사|Cooling Apparatus of a Fuel Cell and Method for thereof|DE102020104553A1|2020-02-20|2020-07-09|FEV Software and Testing Solutions GmbH|Conditioning device for air supply to fuel cells|
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申请号 | 申请日 | 专利标题 ATA51197/2016A|AT519349B1|2016-12-30|2016-12-30|PEM fuel cell|ATA51197/2016A| AT519349B1|2016-12-30|2016-12-30|PEM fuel cell| JP2019535775A| JP2020516010A|2016-12-30|2017-12-01|PEM fuel cell| KR1020197022379A| KR20190099063A|2016-12-30|2017-12-01|PEM Fuel Cell| CA3048938A| CA3048938A1|2016-12-30|2017-12-01|Pem fuel cell| PCT/EP2017/081122| WO2018121957A1|2016-12-30|2017-12-01|Pem fuel cell| DE112017006675.1T| DE112017006675A5|2016-12-30|2017-12-01|PEM fuel cell| CN201780081279.2A| CN110114921A|2016-12-30|2017-12-01|Proton Exchange Membrane Fuel Cells| 相关专利
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