US20010055707A1 - Apparatus for improving the cold starting capability of an electrochemical fuel cell - Google Patents

Apparatus for improving the cold starting capability of an electrochemical fuel cell Download PDF

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US20010055707A1
US20010055707A1 US09/819,875 US81987501A US2001055707A1 US 20010055707 A1 US20010055707 A1 US 20010055707A1 US 81987501 A US81987501 A US 81987501A US 2001055707 A1 US2001055707 A1 US 2001055707A1
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stack
fuel cell
purge
fluid
reactant
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US09/819,875
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Joy Roberts
Jean St-Pierre
Marian van der Geest
Abderrahmane Atbi
Nicholas Fletcher
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Ballard Power Systems Inc
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Ballard Power Systems Inc
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Priority to US09/819,875 priority Critical patent/US20010055707A1/en
Assigned to BALLARD POWER SYSTEMS, INC. reassignment BALLARD POWER SYSTEMS, INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: VAN DER GEEST, MARIAN E., FLETCHER, NICHOLAS J., ATBI, ABDERRAHMANE, ROBERTS, JOY A., ST.-PIERRE, JEAN
Publication of US20010055707A1 publication Critical patent/US20010055707A1/en
Priority to US10/833,228 priority patent/US7482085B2/en
Abandoned legal-status Critical Current

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    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00Fuel cells; Manufacture thereof
    • H01M8/04Auxiliary arrangements, e.g. for control of pressure or for circulation of fluids
    • H01M8/04007Auxiliary arrangements, e.g. for control of pressure or for circulation of fluids related to heat exchange
    • H01M8/04029Heat exchange using liquids
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00Fuel cells; Manufacture thereof
    • H01M8/02Details
    • H01M8/0202Collectors; Separators, e.g. bipolar separators; Interconnectors
    • H01M8/0267Collectors; Separators, e.g. bipolar separators; Interconnectors having heating or cooling means, e.g. heaters or coolant flow channels
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00Fuel cells; Manufacture thereof
    • H01M8/04Auxiliary arrangements, e.g. for control of pressure or for circulation of fluids
    • H01M8/04007Auxiliary arrangements, e.g. for control of pressure or for circulation of fluids related to heat exchange
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00Fuel cells; Manufacture thereof
    • H01M8/04Auxiliary arrangements, e.g. for control of pressure or for circulation of fluids
    • H01M8/04223Auxiliary arrangements, e.g. for control of pressure or for circulation of fluids during start-up or shut-down; Depolarisation or activation, e.g. purging; Means for short-circuiting defective fuel cells
    • H01M8/04225Auxiliary arrangements, e.g. for control of pressure or for circulation of fluids during start-up or shut-down; Depolarisation or activation, e.g. purging; Means for short-circuiting defective fuel cells during start-up
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00Fuel cells; Manufacture thereof
    • H01M8/04Auxiliary arrangements, e.g. for control of pressure or for circulation of fluids
    • H01M8/04223Auxiliary arrangements, e.g. for control of pressure or for circulation of fluids during start-up or shut-down; Depolarisation or activation, e.g. purging; Means for short-circuiting defective fuel cells
    • H01M8/04228Auxiliary arrangements, e.g. for control of pressure or for circulation of fluids during start-up or shut-down; Depolarisation or activation, e.g. purging; Means for short-circuiting defective fuel cells during shut-down
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00Fuel cells; Manufacture thereof
    • H01M8/04Auxiliary arrangements, e.g. for control of pressure or for circulation of fluids
    • H01M8/04223Auxiliary arrangements, e.g. for control of pressure or for circulation of fluids during start-up or shut-down; Depolarisation or activation, e.g. purging; Means for short-circuiting defective fuel cells
    • H01M8/04253Means for solving freezing problems
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00Fuel cells; Manufacture thereof
    • H01M8/04Auxiliary arrangements, e.g. for control of pressure or for circulation of fluids
    • H01M8/04223Auxiliary arrangements, e.g. for control of pressure or for circulation of fluids during start-up or shut-down; Depolarisation or activation, e.g. purging; Means for short-circuiting defective fuel cells
    • H01M8/04268Heating of fuel cells during the start-up of the fuel cells
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00Fuel cells; Manufacture thereof
    • H01M8/04Auxiliary arrangements, e.g. for control of pressure or for circulation of fluids
    • H01M8/04298Processes for controlling fuel cells or fuel cell systems
    • H01M8/043Processes for controlling fuel cells or fuel cell systems applied during specific periods
    • H01M8/04303Processes for controlling fuel cells or fuel cell systems applied during specific periods applied during shut-down
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00Fuel cells; Manufacture thereof
    • H01M8/24Grouping of fuel cells, e.g. stacking of fuel cells
    • H01M8/241Grouping of fuel cells, e.g. stacking of fuel cells with solid or matrix-supported electrolytes
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00Fuel cells; Manufacture thereof
    • H01M8/24Grouping of fuel cells, e.g. stacking of fuel cells
    • H01M8/2457Grouping of fuel cells, e.g. stacking of fuel cells with both reactants being gaseous or vaporised
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00Fuel cells; Manufacture thereof
    • H01M8/10Fuel cells with solid electrolytes
    • H01M2008/1095Fuel cells with polymeric electrolytes
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M2300/00Electrolytes
    • H01M2300/0017Non-aqueous electrolytes
    • H01M2300/0065Solid electrolytes
    • H01M2300/0082Organic polymers
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00Fuel cells; Manufacture thereof
    • H01M8/04Auxiliary arrangements, e.g. for control of pressure or for circulation of fluids
    • H01M8/04082Arrangements for control of reactant parameters, e.g. pressure or concentration
    • H01M8/04089Arrangements for control of reactant parameters, e.g. pressure or concentration of gaseous reactants
    • H01M8/04119Arrangements for control of reactant parameters, e.g. pressure or concentration of gaseous reactants with simultaneous supply or evacuation of electrolyte; Humidifying or dehumidifying
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00Fuel cells; Manufacture thereof
    • H01M8/04Auxiliary arrangements, e.g. for control of pressure or for circulation of fluids
    • H01M8/04082Arrangements for control of reactant parameters, e.g. pressure or concentration
    • H01M8/04089Arrangements for control of reactant parameters, e.g. pressure or concentration of gaseous reactants
    • H01M8/04119Arrangements for control of reactant parameters, e.g. pressure or concentration of gaseous reactants with simultaneous supply or evacuation of electrolyte; Humidifying or dehumidifying
    • H01M8/04156Arrangements 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
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/30Hydrogen technology
    • Y02E60/50Fuel cells

Definitions

  • the present invention relates to techniques to improve the cold start capability of an electrochemical fuel cell. More particularly, the present invention relates to apparatus for improving the cold start capability of fuel cell electric power generation systems that include a solid polymer fuel cell stack.
  • Electrochemical fuel cells convert fuel and oxidant to electricity and reaction product.
  • Solid polymer electrochemical fuel cells generally employ a membrane electrode assembly (“MEA”), which comprises an ion exchange membrane or solid polymer electrolyte disposed between two electrodes typically comprising a layer of porous, electrically conductive sheet material, such as carbon fiber paper or carbon cloth.
  • MEA membrane electrode assembly
  • the MEA contains a layer of catalyst, typically in the form of finely comminuted platinum, at each membrane/electrode interface to induce the desired electrochemical reaction.
  • the electrodes are electrically coupled to provide a circuit for conducting electrons between the electrodes through an external circuit.
  • the fuel stream moves through the porous anode substrate and is oxidized at the anode electrocatalyst layer.
  • the oxidant stream moves through the porous cathode substrate and is reduced at the cathode electrocatalyst layer to form a reaction product.
  • the catalyzed reaction at the anode produces hydrogen cations (protons) from the fuel supply.
  • the ion exchange membrane facilitates the migration of protons from the anode to the cathode.
  • the membrane isolates the hydrogen-containing fuel stream from the oxygen-containing oxidant stream.
  • oxygen reacts with the protons that have crossed the membrane to form water as the reaction product.
  • the MEA is disposed between two electrically conductive fluid flow field plates or separator plates.
  • Fluid flow field plates have at least one flow passage formed in at least one of the major planar surfaces thereof.
  • the flow passages direct the fuel and oxidant to the respective electrodes, namely, the anode on the fuel side and the cathode on the oxidant side.
  • the fluid flow field plates act as current collectors, provide support for the electrodes, provide access channels for the fuel and oxidant to the respective anode and cathode surfaces, and provide channels for the removal of reaction products, such as water, formed during operation of the cell.
  • Separator plates typically do not have flow passages formed in the surfaces thereof, but are used in combination with an adjacent layer of material which provides access passages for the fuel and oxidant to the respective anode and cathode electrocatalyst, and provides passages for the removal of reaction products.
  • the preferred operating temperature range for solid polymer fuel cells is typically 50° C. to 120° C., most typically about 75° C. to 85° C.
  • Two or more fuel cells can be electrically connected together in series to increase the overall power output of the assembly.
  • one side of a given fluid flow field or separator plate can serve as an anode plate for one cell and the other side of the fluid flow field or separator plate can serve as the cathode plate for the adjacent cell.
  • Such a multiple fuel cell arrangement is referred to as a fuel cell stack, and is usually held together in its assembled state by tie rods and end plates.
  • the stack typically includes inlet ports and manifolds for directing the fluid fuel stream (such as substantially pure hydrogen, methanol reformate or natural gas reformate, or a methanol-containing stream in a direct methanol fuel cell) and the fluid oxidant stream (such as substantially pure oxygen, oxygen-containing air or oxygen in a carrier gas such as nitrogen) to the individual fuel cell reactant flow passages.
  • the stack also commonly includes an inlet port and manifold for directing a coolant fluid stream, typically water, to interior passages within the stack to absorb heat generated by the fuel cell during operation.
  • the stack also generally includes exhaust manifolds and outlet ports for expelling the depleted reactant streams and the reaction products such as water, as well as an exhaust manifold and outlet port for the coolant stream exiting the stack.
  • various fuel, oxidant and coolant conduits carry these fluid streams to and from the fuel cell stack.
  • Solid polymer fuel cells generally employ perfluorosulfonic ion exchange membranes, such as those sold by DuPont under its NAFION trade designation and by Dow under the trade designation XUS 13204.10.
  • perfluorosulfonic ion exchange membranes such as those sold by DuPont under its NAFION trade designation and by Dow under the trade designation XUS 13204.10.
  • the fuel and oxidant reactant streams are typically humidified before they are introduced to solid polymer fuel cells so as to facilitate proton transport through the ion exchange membrane and to avoid drying (and damaging) the membrane separating the anode and cathode of each cell.
  • Each reactant stream exiting the fuel cell stack generally contains water.
  • the outlet fuel stream from the anodes generally contains the water added to humidify the incoming fuel stream plus any product water drawn across the membrane from the cathode.
  • the outlet oxidant stream from the cathodes generally contains the water added to humidify the incoming oxidant stream plus product water formed at the cathode.
  • the freezing temperature of water means the freezing temperature of free water, that is, 0° C. at 1 atmosphere. It may also be necessary or desirable when ceasing operation of the solid polymer fuel cell stack to improve the cold start capability and freeze tolerance of the stack by reducing the amount of water remaining within the fuel, oxidant and coolant passages of the stack. Upon freezing, water remaining within stack passages will expand and potentially damage structures within the stack such as, for example, the membrane/electrocatalyst interface, the reactant passageways, conduits and seals, as well as the porous electrode substrate material.
  • a measure of electrochemical fuel cell performance is the voltage output from the cell for a given current density. Higher performance is associated with a higher voltage output for a given current density or higher current density for a given voltage output.
  • an electric power generation system includes a fuel cell stack connectable to an external electrical circuit; when so connected, the stack may supply electric current to the external circuit.
  • the stack comprises at least one solid polymer fuel cell and fluid stream passages for directing fluid streams through at least one of the fuel cells.
  • the system also includes a purge system that has a purge conduit having an inlet end connectable to a purge fluid supply, and an outlet end connectable to at least one of the fluid stream passages.
  • the purge system also has a purge flow control device that controls the flow of a pressurized purge fluid through the purge conduit such that water can be purged from at least one of the fluid stream passages after a supply of electric current from the stack to the external circuit has been interrupted.
  • the purge system is operable to improve the cold start capability and freeze tolerance of its fuel cell stacks by reducing the amount of water remaining within the passages of the stack prior to stack freezing.
  • the fluid stream passages of the stack include passages for oxidant and fuel reactant streams. Any or all of the oxidant and fuel stream passages can connected to the purge conduit upstream of the stack, so that purge fluid can be directed to one or both of the oxidant and fuel passages and through the fuel cell(s). Additionally, a coolant passage may be connected to the purge conduit upstream of the stack to enable purge fluid to be transmitted therethrough.
  • the purge flow control device controls the purge operation during stack shut-down.
  • a suitable purge flow control device includes a control valve connected to the purge conduit, and a control unit that is communicative with at least the control valve and optionally with one or more additional devices and sensors.
  • the control unit is a microcontroller that is responsive to one or more input signals, and can control one or more devices. Upon receipt of an input signal to shut down the stack, the microcontroller opens a switch connecting the stack to the external circuit, thereby interrupting the supply of current from the stack to the circuit. Then, the control unit shuts off the reactant flow and opens the purge control valve for a selected period of time.
  • the purge system may further include a pressure regulator connected to the purge conduit and communicative with the control unit, to enable regulation of the pressure of purge fluid supplied to at least one of the reactant passages.
  • a suitable purge fluid is an inert gas, such as nitrogen. “Inert” in this sense means a fluid that is substantially non-reactive in the fuel cell.
  • an electric power generation system that has a humidifier bypass system.
  • Such an electric power generation system comprises a fuel cell stack connectable to an external electrical circuit; when connected, the stack may supply electric current to the external circuit.
  • the stack comprises at least one solid polymer fuel cell, reactant stream passages for directing reactant streams through at least one of the fuel cells, a humidifier in fluid communication with at least one of the reactant stream passages for humidifying a reactant stream supplied to the fuel cell stack, and a humidifier bypass system.
  • the humidifier bypass system comprises at least one bypass conduit for transmitting at least one reactant from a reactant supply to the stack in fluid isolation from the humidifier, and a bypass control device for selectively directing flow of the reactant streams to the fuel cell stack through the humidifier or the humidifier bypass conduit.
  • Each bypass conduit typically includes an inlet end that is connected to one of the reactant stream passages upstream of the humidifier or directly to one of the reactant supplies, and an outlet end that is connected to one of the reactant stream inlet passages downstream of said humidifier and upstream of the stack.
  • the control device is operable to direct reactant fluid through the humidifier and to the stack during normal operation, that is, while electrical power is being generated by the stack, and through the bypass conduit and to the stack during a shut down procedure (for example, after supply of electric current from the stack to the external circuit has been interrupted).
  • the control device may include at least one bypass inlet valve connected to one of the reactant passages upstream of the humidifier, and at least one bypass outlet valve connected to the same reactant passage downstream of the humidifier.
  • the bypass conduit connects the bypass inlet and outlet valves so that reactant fluid can be transmitted in fluid isolation from the humidifier directly to the stack.
  • the bypass control device preferably further includes a control unit communicative with the bypass inlet and outlet valves and with an input signal source.
  • the control unit may be a micro-controller or other similar device.
  • FIG. 1 is an exploded side view of a typical solid polymer electrochemical fuel cell with a membrane electrode assembly interposed between two fluid flow field plates.
  • FIG. 2 is a perspective cut-away view of an electrochemical fuel cell stack.
  • FIG. 3 is a schematic diagram of a fuel cell electric power generation system incorporating a nitrogen gas purge system.
  • FIG. 4 is a schematic diagram of a fuel cell electric power generation system incorporating a humidifier bypass purge system.
  • FIG. 5 is a composite plot of fuel cell stack voltage versus time in minutes (plot A) and fuel cell stack core temperature versus time in minutes (plot B) for a 10-cell stack, operation of which was commenced after the stack had equilibrated at a core temperature of ⁇ 11° C.
  • FIG. 6 is a composite plot of fuel cell stack voltage versus time in minutes (plot C) and fuel cell stack core temperature versus time in minutes (plot D) for a 4 cell stack, operation of which was commenced at a core temperature of ⁇ 19° C.
  • FIG. 7 is a plot of voltage as a function of current density for a fuel cell containing a membrane electrode assembly with a DowPontTM membrane exposed to three cold purge freeze/thaw cycles.
  • FIG. 8 is a plot of voltage as a function of current density for the fuel cell containing a membrane electrode assembly with a Nafion® 1135 membrane exposed to three cold purge freeze/thaw cycles.
  • FIG. 9 is a plot of voltage as a function of current density for a fuel cell containing a membrane electrode assembly with a Nafion® 1135 membrane exposed to one shorter duration cold purge freeze/thaw cycle.
  • FIG. 10 is a plot of voltage as a function of current density for a fuel cell containing a membrane electrode assembly with a DowPontTM membrane exposed to three hot purge freeze/thaw cycles.
  • FIG. 11 is a plot of voltage as a function of current density for the fuel cell containing a membrane electrode assembly with a Nafion® 1135 membrane exposed to three hot purge freeze/thaw cycles.
  • FIG. 12 is a plot of cell voltage, for the fuel cell containing a membrane electrode assembly with a Nafion® 112 membrane, after each of a series of 55 cold purge freeze/thaw cycles.
  • FIG. 13 is a plot of stack voltage against operating time for an 8-cell Ballard Mark 513 fuel cell stack which was subjected to a series of freeze-thaw-operation cycles, interspersed with four heat treatment cycles.
  • FIG. 14 is a plot of stack voltage against current density for the fuel cell stack used to generate the data of FIG. 12, before and after heat treatment
  • FIG. 1 illustrates a typical fuel cell 10 .
  • Fuel cell 10 includes a membrane electrode assembly 12 interposed between anode flow field plate 14 and cathode flow field plate 16 .
  • Membrane electrode assembly 12 consists of an ion exchange membrane 20 interposed between two electrodes, namely, anode 21 and cathode 22 .
  • anode 21 and cathode 22 comprise a substrate of porous electrically conductive sheet material 23 and 24 , respectively, for example, carbon fiber paper or carbon cloth.
  • Each substrate has a thin layer of electrocatalyst 25 and 26 , respectively, disposed on one surface thereof at the interface with membrane 20 to render each electrode electrochemically active.
  • anode flow field plate 14 has at least one fuel flow channel 14 a formed in its surface facing anode 21 .
  • cathode separator plate 16 has at least one oxidant flow channel 16 a formed in its surface facing cathode 22 .
  • channels 14 a and 16 a form the reactant flow field passages for the fuel and oxidant, respectively.
  • the flow field plates are electrically conductive.
  • a fuel cell stack 100 includes a plurality of fuel cell assemblies, a series of which is designated as 111 in FIG. 2. Each of the fuel cell assemblies includes a membrane electrode assembly 112 interposed between a pair of fluid flow field plates 114 , 116 . Fuel cell stack 100 also includes a first end plate 130 and a second end plate 140 .
  • Plate 130 includes fluid inlet ports 132 , 134 , 136 for introducing fluid fuel, oxidant and coolant streams, respectively, to the stack.
  • Plate 140 includes fluid outlet ports 142 , 144 , 146 for exhausting fluid fuel, oxidant and coolant streams, respectively, from the stack.
  • the fluid outlet ports are fluidly connected to the corresponding fluid inlet ports via passages within the stack.
  • the fuel cell assemblies have a series of openings formed therein, which cooperate with corresponding openings in adjacent assemblies to form fluid manifolds 152 , 154 , 156 , 162 , 164 , 166 within the stack 100 .
  • the fluid manifolds are each circumscribed by a sealant material or gasket.
  • a peripheral seal at the exterior perimeter of each fuel cell fluidly isolates the interior, electrochemically active portion of the fuel cell from the external environment.
  • a fuel stream entering the stack via fuel inlet port 132 is directed to the individual fuel flow field plates via manifold 152 . After passing through the fuel flow field plate channels, the fuel stream is collected in manifold 162 and exhausted from the stack via fuel outlet port 142 . Similarly, an oxidant stream entering the stack via oxidant inlet port 134 is directed to individual oxidant flow field plates via manifold 154 . After passing through the oxidant flow field plate channels, the oxidant stream is collected in manifold 164 and exhausted from the stack via oxidant outlet port 144 .
  • a fluid coolant (typically water) introduced via coolant inlet port 136 is directed to coolant plate assemblies (not shown) in the stack 100 via manifold 156 .
  • Coolant manifolds 156 , 166 may be fitted with a compliant mechanism (not shown), such as tube cushions or inserts made of closed cell foam, to accommodate the expansion of freezing water.
  • Tie rods 170 extend between end plates 130 and 140 to compress and secure stack 100 in its assembled state with fastening nuts 172 disposed at opposite ends of each tie rod, and disc springs 174 interposed between the fastening nuts 172 and end plates 130 , 140 .
  • FIG. 3 is a schematic diagram of a fuel cell electric power generation system 200 comprising a fuel cell stack 210 and a nitrogen gas purge system 250 .
  • the fuel cell stack 210 includes negative and positive bus plates 212 , 214 , respectively, to which an external circuit comprising a variable load 216 is electrically connectable to the stack 210 by closing switch 218 .
  • the system includes a fuel (hydrogen) circuit, an oxidant (air) circuit, and a coolant water circuit.
  • the reactant and coolant streams are circulated in the system 200 in various conduits illustrated schematically in FIG. 3.
  • a hydrogen supply 220 is connected to the stack 210 ; hydrogen pressure is controllable by pressure regulator 221 . Water in the hydrogen stream exiting the stack 210 is accumulated in a knock drum 222 , which can be drained by opening valve 223 . Unreacted hydrogen is recirculated to stack 210 by a pump 224 in recirculation loop 225 . An air supply 230 is connected to the stack 210 , the pressure of which is controllable by pressure regulator 231 . Water in the air stream exiting the stack 210 is accumulated in reservoir 232 , which can be drained by opening valve 233 , and the air stream is vented from the system via valve 234 .
  • coolant water loop 240 water is pumped from reservoir 232 and circulated through stack 210 by pump 241 .
  • the temperature of the water is adjusted in a heat exchanger 242 .
  • Purge system 250 is used to purge the hydrogen and oxidant passages in fuel cell stack 210 with a low humidity, non-reactive gas such as nitrogen.
  • Flow of purge gas from a purge gas supply 260 to the hydrogen and air inlet passages 261 , 262 is transmitted through purge supply conduits 268 , 269 and three way valves 266 , 267 connected to respective hydrogen and air inlet passages 261 , 262 upstream of the stack 210 .
  • the flow of nitrogen through each purge conduit 268 , 269 is controlled by respective flow regulating valves 263 , 264 .
  • a micro-controller (not shown) or similar electronic control unit may be provided to automate at least some of the purge system operation.
  • the microcontroller is programmed to control valves 221 , 231 , 263 , 264 , 265 266 , 267 , and switch 218 .
  • the micro-controller opens switch 218 to interrupt the flow of electricity from the stack 210 to the circuit, then closes air and hydrogen supply valves 221 , 231 and opens valves 263 , 264 , 266 , 267 to enable purge fluid to be transmitted through conduits 268 , 269 to air and hydrogen conduits 261 , 262 and through the stack 210 .
  • An additional purge conduit and three way valve may be connected to the coolant loop upstream of the stack 210 to enable purging of the coolant loop during the shut down procedure.
  • the micro-controller is adapted accordingly to shut down pump 241 and heat exchanger 242 prior to directing purge fluid to the coolant loop.
  • the reactant streams themselves can be employed as the purge streams.
  • the purge fluid if it is a gas, is dry or at least not humidified.
  • reactant stream humidifiers if any are bypassed to provide streams having water carrying capacity greater than humidified reactant streams.
  • a humidifier bypass purge system 300 replaces the nitrogen gas purge system 250 and comprises a series of valves and conduits that cooperate to direct the supply oxidant and fuel streams in fluid isolation from a humidifier.
  • upstream three-way bypass valves 302 , 304 are provided on respective fuel and oxidant inlet passages 261 , 262 between the oxidant and fuel supply sources 220 , 230 , and a humidifier 306 .
  • the humidifier 306 is preferably a contact-type gas humidifier; however other types of humidifiers known to a person skilled in the art can be used, for example, a membrane humidifier.
  • a fuel bypass conduit 308 is connected to upstream fuel bypass valve 302 and to a downstream three-way valve 267 connected to fuel inlet passage 261 downstream of humidifier 306 and upstream of stack 210 .
  • an oxidant bypass conduit 310 is connected to upstream oxidant bypass valve 304 and to a downstream three-way valve 266 connected to the oxidant inlet passage 262 downstream of the humidifier 306 and upstream of stack 210 .
  • the respective oxidant and fuel upstream and downstream bypass valves 302 , 304 , 267 , 266 are operated to direct reactant flow through humidifier 306 and to stack 210 during normal stack operation, and through bypass conduits 308 , 310 to stack 210 during a purging operation.
  • the bypass conduits 308 , 310 are in fluid isolation from the humidifier 306 , reactant supplied to the stack 210 via the bypass conduits 308 , 310 avoid humidification.
  • a control device (not shown ) similar to that used to control the purge system 250 may be programmed to control the humidification bypass operation.
  • FIG. 5 is a composite plot of fuel cell stack voltage versus time in minutes (plot A) and fuel cell stack core temperature versus time in minutes (plot B) for a 10-cell stack to which the flow of fuel and oxidant was restored after the stack had equilibrated at a core temperature of ⁇ 11° C.
  • the stack had been operating previously, and therefore the reactant flow passages contained moist gases.
  • the reactant and coolant water passages within the stack were purged by circulating dry, compressed air through them.
  • the stack core temperature was then lowered below the freezing temperature of water by exposing the stack to a surrounding environment with a temperature below the freezing temperature of water.
  • the stack was typically placed in an insulated chamber, with the fluid and electrical connections to the stack fitted through the chamber walls. Cold nitrogen gas from a liquid nitrogen source was circulated through the chamber.
  • the stack core temperature was measured using a thermocouple positioned in a thermally conductive plate located between two fuel cells in the center of the stack. Stack voltage, stack current and ambient temperature were also monitored.
  • FIG. 6 is a composite plot of fuel cell stack voltage versus time in minutes (plot C) and fuel cell stack core temperature versus time in minutes (plot D) for a 4-cell stack, operation of which was commenced at a core temperature of ⁇ 19° C.
  • the reactant passages within the stack were purged by circulating dry nitrogen. Coolant water remained in the coolant passages.
  • the purge fluid is an inert gas such as nitrogen. Circulation of hydrogen and air was commenced with a load (50 amp) connected. Approximately 2 minutes transpired before the output current reached 50 amps. The load was increased to 260 amps once the stack reached about 30° C., and the coolant pump was then activated. One cell in the stack was not operating properly; hence the lower than normal average cell voltages.
  • the fluid coolant stream is not circulated until the stack has reached a temperature at or near the desired stack operating temperature.
  • the circulating fluid coolant stream assuming it is not preheated, will absorb and carry away heat otherwise available to warm the stack. Refraining from circulating the fluid coolant stream therefore expedites the warming of the stack to its desired operating temperature.
  • freeze tolerance refers to the ability of a fuel cell or fuel cell stack to maintain substantially the same performance after one or more freeze/thaw cycles.
  • the reactant passages including the manifolds and individual fuel cell reactant flow passages within a fuel cell stack, are preferably purged with a fluid stream before the temperature of the stack is decreased to below the freezing temperature of water.
  • a fluid which is not reactive in the fuel cell environment such as nitrogen gas
  • a liquid may be used as the purge fluid.
  • it would be a liquid that does not freeze at the temperature to which the fuel cell is to be exposed, and which has no detrimental effect on the fuel cell components.
  • cold purging it has been found that improved cold start capability and freeze tolerance of fuel cells to multiple freeze/thaw cycles can also be achieved when one or more of the fuel, oxidant, coolant and humidification passages are purged after the stack core temperature has been reduced to at or below normal room temperature (hereinafter referred to as “cold purging”).
  • hot purging The beneficial effect of purging is not quite so pronounced when the stack passages are purged at a temperature within the normal stack operating temperature range (hereinafter referred to as “hot purging”).
  • both MEAs had 3.87 mg/cm 2 platinum black electrocatalyst applied by hand to carbon fiber paper.
  • the Nafion® 1135 membrane employed in MEA No. 513-15 had an equivalent weight of 1100 and a thickness of about 85 ⁇ m (dry).
  • the DowPontTM membrane employed in MEA No. 513-22 had an equivalent weight of 800 and a thickness of about 100 ⁇ m (wet).
  • the Mark 513 cell was assembled and run overnight at 600 ASF (6458 ASM) at an air/fuel pressure of 30/30 psig (207/207 kPa gauge) and a stoichiometry of 2/1.5 respectively.
  • the fuel was substantially pure hydrogen.
  • “Stoichiometry” is the ratio of the amount of reactant supplied to the fuel cell stack to the amount of reactant actually consumed in the fuel cell stack. In this instance, a fuel stoichiometry of 1.5 means that 150 parts of hydrogen are supplied to the fuel cell for each 100 parts actually consumed in the fuel cell.
  • the cell was cooled from its normal operating temperature (approximately 85° C.) to room temperature (approximately 23° C.) before purging. In each case, the fuel, oxidant, coolant and humidification passages were purged for approximately 7 minutes with nitrogen.
  • the cell containing the Nafion® 1135 membrane was taken through a fourth freeze/thaw cycle with a purge duration of only approximately 1 minute (results shown in FIG. 8).
  • the cell inlets and outlets were capped and the cell was placed in a freezer. Internal sealing pressure within the cell was maintained during freezing. The freezer temperature was approximately ⁇ 20° C.
  • the duration of the freeze ranged from 15-20 hours. After removal from the freezer, the coolant lines were connected and the cell was heated to 50° C. At that point, operation of the fuel cell was commenced at 50 ASF (538.2 ASM) with excess fuel and oxidant flow rates. When the cell temperature reached 60° C., the current density was increased to 600 ASF (6458 ASM) and the cell was operated for at least one hour or until cell voltage had stabilized. A polarization test from 0 to 1000 ASF (0 to 10764 ASM) was performed for each of the two MEAs tested, using two different oxidant streams: air and substantially pure oxygen.
  • FIG. 7 is a plot of voltage as a function of current density for the fuel cell containing MEA 513-22 (DowPontTM membrane).
  • Plots 1 - 4 show the performance on air prior to freezing (which is the plot with the solid line and solid data points ⁇ ), and after each of the three cold purge freeze/thaw cycles described above.
  • Plots 5 - 8 show the performance on oxygen prior to freezing (which is the plot with the solid line and solid data points ⁇ ), and after each of the three cold purge freeze/thaw cycles described above.
  • the four plots in FIG. 7 are difficult to distinguish from one another.
  • FIG. 8 is a plot of voltage as a function of current density for the fuel cell containing MEA 513-12 (Nafion® 1135 membrane).
  • Plots 1 - 4 show the performance on air prior to freezing (which is the plot with the solid line and solid data points ⁇ ), and after each of the three cold purge freeze/thaw cycles described above.
  • Plots 5 - 8 show the performance on oxygen prior to freezing (which is the plot with the solid line and solid data points ⁇ ), and after each of the three cold purge freeze/thaw cycles described above. Again, for each of the oxidant streams, the four plots in FIG. 8 are difficult to distinguish from one another.
  • FIG. 9 is a plot of voltage as a function of current density for the fuel cell containing MEA 513-12 (Nafion® 1135 membrane).
  • Plots 1 - 2 show the performance on air prior to freezing (which is the plot with the solid line and solid data points ⁇ ), and after the fourth cold purge freeze/thaw cycle described above, in which a shorter purge duration (approximately 1 minute) was used.
  • Plots 3 - 4 show the performance on oxygen prior to freezing (which is the plot with the solid line and solid data points ⁇ ) and after the fourth cold purge freeze/thaw cycle described above. Again, for each of the oxidant streams, the two plots in FIG. 8 are difficult to distinguish from one another, indicating that a shorter duration purge can give satisfactory results.
  • each cell was purged at stack operating temperature (approximately 85° C.) before cooling.
  • the fuel, oxidant, coolant and humidification passages were purged for approximately 1 minute with nitrogen.
  • the cell inlets and outlets were capped and the cell was placed in a freezer. Internal sealing pressure within the cell was maintained during freezing.
  • the freezer temperature was approximately ⁇ 20° C.
  • the duration of the freeze ranged from 15-20 hours.
  • the coolant lines were connected and the cell was heated to operating temperature and operation commenced using essentially the same procedure employed for the cold purge freeze/thaw cycles described above.
  • a polarization test from 0 to 1000 ASF (0 to 10764 ASM) was performed for each of the two MEAs tested, again using two different oxidant streams: air and substantially pure oxygen.
  • FIG. 10 is a plot of voltage as a function of current density for the fuel cell containing MEA 513-22 (DowPontTM membrane).
  • Plots 1 - 4 show the performance on air prior to freezing (which is the plot with the solid line and solid data points ⁇ ), and after each of the three hot purge freeze/thaw cycles described above.
  • Plots 5 - 8 show the performance on oxygen prior to freezing (which is the plot with the solid line and solid data points ⁇ ), and after each of the three hot purge freeze/thaw cycles described above.
  • a significant mass transport effect appears to occur at higher current densities on air after the third freeze cycle, based on the increased difference between the air and oxygen performance levels.
  • FIG. 11 is a plot of voltage as a function of current density for the fuel cell containing MEA 513-12 (Nafion® 1135 membrane.
  • Plots 1 - 4 show the performance on air prior to freezing (which is the plot with the solid line and solid data points ⁇ ), and after each of the three hot purge freeze/thaw cycles described above.
  • Plots 5 - 8 show the performance on oxygen prior to freezing (which is the plot with the solid line and solid data points ⁇ ), and after each of the three hot purge freeze/thaw cycles described above. Again, a significant mass transport effect appears to occur at higher current densities on air, based on the progressively increasing difference between the air and oxygen performance levels after each freeze/thaw cycle.
  • the MEA had a screen printed anode containing 0.34-0.38 mg/cm 2 platinum black electrocatalyst and a screen printed cathode containing 0.73-0.82 mg/cm 2 platinum black electrocatalyst on carbon fiber paper, both with a Nafion spray coating (0.2 mg/cm 2 ).
  • the cell was tested in a temperature-controlled environmental chamber at an air/fuel pressure of 27/27 psig (186/186 kPa gauge) and a stoichiometry of 1.8/1.2 respectively.
  • the fuel was a simulated methanol reformate stream (composition 63.5% hydrogen; 22.5% carbon dioxide; 13% nitrogen; 1% methanol and 40 parts per million (ppm) carbon monoxide), and a 4% air bleed was employed at the anode.
  • the fuel and oxidant streams were humidified.
  • the cell was cooled from its normal operating temperature (approximately 80° C.) to a chamber temperature at which no part of the stack was below 0° C., but where the cell temperature was approximately 30° C. before purging.
  • the oxidant passages were purged for approximately 10 seconds with dry (unhumidified) air.
  • the cell inlets and outlets were closed by actuated valves, and the temperature in the chamber was reduced to approximately ⁇ 25° C.
  • the duration of each freeze was approximately 1 hour. Internal sealing pressure within the cell was maintained during freezing. The cell was then thawed to 5° C.
  • FIG. 12 shows the results obtained after each of 55 such cycles with the cell voltage measured once it had stabilized at 1.0 A/cm 2 during the 30 minutes of operation at that current density (Plot A) and once it had stabilized at 0.5 A/cm 2 during the second period of operation at that current density (Plot B).
  • the performance degradation over the 55 cycles was negligible: approximately ⁇ 0.1 mV/cycle at 0.5 A/cm 2 and approximately ⁇ 0.2 mV/cycle at 1.0 A/cm 2 .
  • FIG. 13 shows a plot of stack voltage against operating time for an 8-cell Ballard Mark 513 fuel cell stack which was subjected to a series of freeze-thaw-operation cycles.
  • oxidant and coolant passages Prior to freezing the fuel, oxidant and coolant passages were purged with dry gas.
  • the cell inlets and outlets were capped and the cell was placed in a freezer. Internal sealing pressure within the cell was maintained during freezing.
  • the freezer temperature was approximately ⁇ 20° C. The duration of the freeze in each case was greater than 12 hours. After some cycles the stack was operated normally, and after other cycles the stack operating temperature was increased to above its normal operating temperature for a period, before normal operation was resumed.
  • the stack was operated on humidified air and hydrogen, both at 30 psig (207 kPa gauge), at stoichiometries of 2.0 and 1.5 respectively, at a current density of 700 ASF (7535 ASM) to generate the data shown in FIG. 12.
  • the coolant inlet temperature was 75° C. with a ⁇ T (change in temperature from inlet to outlet) of 10° C. at 1000 ASF (10764 ASM).
  • FIG. 14 shows a plot of stack voltage as a function of current density for the 8-cell Ballard Mark 513 fuel cell stack used to generate the data of FIG. 13.
  • Plots A, B and C show performance curves for operation on air, and plots D, E and F for operation on oxygen.
  • Plots A and D show the stack performance before any of the heat treatments referred to the description of FIG. 13 but after the final freeze cycle
  • plots B and E show the stack performance immediately after the fourth heat treatment
  • plots C and F show the stack performance about 2 days after the fourth heat treatment.
  • the results on air show a substantial and sustained improvement in post-freezing performance after the heat treatment.
  • the improvement is believed to be attributable to improved mass transport in the MEA, based on the fact that on oxygen the performance was not significantly affected by the heat treatment. This indicates that performance loss after freezing may be, at least in part, due to mass transport difficulties in the cells, which have a more significant effect on air than on a substantially pure oxidant stream. These detrimental effects could be due to retained water in the membrane electrode assembly. It is possible that the heat treatment method assists in removing residual water from the membrane electrode assembly, and thereby improves performance at start-up, particularly on air.

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Abstract

An electric power generation system has components that improve the cold start capability and freeze tolerance of a constituent fuel cell stack. The components cooperate to reduce the amount of water remaining within the passages of the stack. The system includes a purge system that is connectable to the oxidant supply, the fuel supply and/or the coolant passages upstream of the stack. When the stack is shut down, the stack is disconnected from an external circuit, and purge fluid is directed by the purge system through the stack before the stack falls below the freezing point of water. In systems where the fuel and/or oxidant streams are humidified prior to their introduction into the stack, a humidifier bypass system may be provided in place of the purge system. The humidifier bypass system directs reactant fluid to the stack in fluid isolation from the humidifier, so that the inlet reactant streams are unhumidified.

Description

    CROSS-REFERENCE TO RELATED APPLICATION(S)
  • This application is a continuation-in-part of U.S. patent application Ser. No. 09/406,318, entitled “Methods for Improving the Cold Starting Capability of an Electrochemical Fuel Cell”. The '318 application is, in turn, a continuation-in-part of U.S. patent application Ser. No. 09/138,625 filed Aug. 24, 1998, entitled “Method and Apparatus for Commencing Operation of a Fuel Cell Electric Power Generation System Below the Freezing Temperature of Water”. The '625 application is, in turn, a continuation of U.S. patent application Ser. No. 08/659,921 filed Jun. 7, 1996, now U.S. Pat. No. 5,798,186 issued Aug. 25, 1998, also entitled “Method and Apparatus for Commencing Operation of a Fuel Cell Electric Power Generation System Below the Freezing Temperature of Water”. The '318, '625 and '921 applications are each hereby incorporated by reference in their entirety.[0001]
  • FIELD OF THE INVENTION
  • The present invention relates to techniques to improve the cold start capability of an electrochemical fuel cell. More particularly, the present invention relates to apparatus for improving the cold start capability of fuel cell electric power generation systems that include a solid polymer fuel cell stack. [0002]
  • BACKGROUND OF THE INVENTION
  • Electrochemical fuel cells convert fuel and oxidant to electricity and reaction product. Solid polymer electrochemical fuel cells generally employ a membrane electrode assembly (“MEA”), which comprises an ion exchange membrane or solid polymer electrolyte disposed between two electrodes typically comprising a layer of porous, electrically conductive sheet material, such as carbon fiber paper or carbon cloth. The MEA contains a layer of catalyst, typically in the form of finely comminuted platinum, at each membrane/electrode interface to induce the desired electrochemical reaction. In operation the electrodes are electrically coupled to provide a circuit for conducting electrons between the electrodes through an external circuit. [0003]
  • At the anode, the fuel stream moves through the porous anode substrate and is oxidized at the anode electrocatalyst layer. At the cathode, the oxidant stream moves through the porous cathode substrate and is reduced at the cathode electrocatalyst layer to form a reaction product. [0004]
  • In fuel cells employing hydrogen as the fuel and oxygen-containing air (or substantially pure oxygen) as the oxidant, the catalyzed reaction at the anode produces hydrogen cations (protons) from the fuel supply. The ion exchange membrane facilitates the migration of protons from the anode to the cathode. In addition to conducting protons, the membrane isolates the hydrogen-containing fuel stream from the oxygen-containing oxidant stream. At the cathode electrocatalyst layer, oxygen reacts with the protons that have crossed the membrane to form water as the reaction product. The anode and cathode reactions in hydrogen/oxygen fuel cells are shown in the following equations: [0005]
  • Anode reaction: H2→2H++2e
  • Cathode reaction: ½O2+2H++2e→H2O
  • In typical fuel cells, the MEA is disposed between two electrically conductive fluid flow field plates or separator plates. Fluid flow field plates have at least one flow passage formed in at least one of the major planar surfaces thereof. The flow passages direct the fuel and oxidant to the respective electrodes, namely, the anode on the fuel side and the cathode on the oxidant side. The fluid flow field plates act as current collectors, provide support for the electrodes, provide access channels for the fuel and oxidant to the respective anode and cathode surfaces, and provide channels for the removal of reaction products, such as water, formed during operation of the cell. Separator plates typically do not have flow passages formed in the surfaces thereof, but are used in combination with an adjacent layer of material which provides access passages for the fuel and oxidant to the respective anode and cathode electrocatalyst, and provides passages for the removal of reaction products. The preferred operating temperature range for solid polymer fuel cells is typically 50° C. to 120° C., most typically about 75° C. to 85° C. [0006]
  • Two or more fuel cells can be electrically connected together in series to increase the overall power output of the assembly. In series arrangements, one side of a given fluid flow field or separator plate can serve as an anode plate for one cell and the other side of the fluid flow field or separator plate can serve as the cathode plate for the adjacent cell. Such a multiple fuel cell arrangement is referred to as a fuel cell stack, and is usually held together in its assembled state by tie rods and end plates. The stack typically includes inlet ports and manifolds for directing the fluid fuel stream (such as substantially pure hydrogen, methanol reformate or natural gas reformate, or a methanol-containing stream in a direct methanol fuel cell) and the fluid oxidant stream (such as substantially pure oxygen, oxygen-containing air or oxygen in a carrier gas such as nitrogen) to the individual fuel cell reactant flow passages. The stack also commonly includes an inlet port and manifold for directing a coolant fluid stream, typically water, to interior passages within the stack to absorb heat generated by the fuel cell during operation. The stack also generally includes exhaust manifolds and outlet ports for expelling the depleted reactant streams and the reaction products such as water, as well as an exhaust manifold and outlet port for the coolant stream exiting the stack. In a power generation system various fuel, oxidant and coolant conduits carry these fluid streams to and from the fuel cell stack. [0007]
  • When an electrical load (comprising one or more load elements) is placed in an electrical circuit connecting the electrodes, the fuel and oxidant are consumed in direct proportion to the electrical current drawn by the load, which will vary with the ohmic resistance of the load. [0008]
  • Solid polymer fuel cells generally employ perfluorosulfonic ion exchange membranes, such as those sold by DuPont under its NAFION trade designation and by Dow under the trade designation XUS 13204.10. When employing such membranes, the fuel and oxidant reactant streams are typically humidified before they are introduced to solid polymer fuel cells so as to facilitate proton transport through the ion exchange membrane and to avoid drying (and damaging) the membrane separating the anode and cathode of each cell. [0009]
  • Each reactant stream exiting the fuel cell stack generally contains water. The outlet fuel stream from the anodes generally contains the water added to humidify the incoming fuel stream plus any product water drawn across the membrane from the cathode. The outlet oxidant stream from the cathodes generally contains the water added to humidify the incoming oxidant stream plus product water formed at the cathode. [0010]
  • In some fuel cell applications, such as, for example, motive applications, it may be necessary or desirable to commence operation of a solid polymer electrolyte fuel cell stack when the stack core temperature is below the freezing temperature of water. As used herein, the freezing temperature of water means the freezing temperature of free water, that is, 0° C. at 1 atmosphere. It may also be necessary or desirable when ceasing operation of the solid polymer fuel cell stack to improve the cold start capability and freeze tolerance of the stack by reducing the amount of water remaining within the fuel, oxidant and coolant passages of the stack. Upon freezing, water remaining within stack passages will expand and potentially damage structures within the stack such as, for example, the membrane/electrocatalyst interface, the reactant passageways, conduits and seals, as well as the porous electrode substrate material. [0011]
  • If there is an expectation that a solid polymer fuel cell stack will be subjected to cold temperatures, especially temperatures below the freezing temperature of water, one or more special start-up and shutdown techniques and associated apparatus may be used. These techniques may improve the cold start capability and freeze tolerance of the stack, and improve the subsequent fuel cell performance. A measure of electrochemical fuel cell performance is the voltage output from the cell for a given current density. Higher performance is associated with a higher voltage output for a given current density or higher current density for a given voltage output. [0012]
  • SUMMARY OF THE INVENTION
  • According to one aspect of the invention, an electric power generation system is provided that includes a fuel cell stack connectable to an external electrical circuit; when so connected, the stack may supply electric current to the external circuit. The stack comprises at least one solid polymer fuel cell and fluid stream passages for directing fluid streams through at least one of the fuel cells. The system also includes a purge system that has a purge conduit having an inlet end connectable to a purge fluid supply, and an outlet end connectable to at least one of the fluid stream passages. The purge system also has a purge flow control device that controls the flow of a pressurized purge fluid through the purge conduit such that water can be purged from at least one of the fluid stream passages after a supply of electric current from the stack to the external circuit has been interrupted. The purge system is operable to improve the cold start capability and freeze tolerance of its fuel cell stacks by reducing the amount of water remaining within the passages of the stack prior to stack freezing. [0013]
  • The fluid stream passages of the stack include passages for oxidant and fuel reactant streams. Any or all of the oxidant and fuel stream passages can connected to the purge conduit upstream of the stack, so that purge fluid can be directed to one or both of the oxidant and fuel passages and through the fuel cell(s). Additionally, a coolant passage may be connected to the purge conduit upstream of the stack to enable purge fluid to be transmitted therethrough. [0014]
  • The purge flow control device controls the purge operation during stack shut-down. A suitable purge flow control device includes a control valve connected to the purge conduit, and a control unit that is communicative with at least the control valve and optionally with one or more additional devices and sensors. In one aspect, the control unit is a microcontroller that is responsive to one or more input signals, and can control one or more devices. Upon receipt of an input signal to shut down the stack, the microcontroller opens a switch connecting the stack to the external circuit, thereby interrupting the supply of current from the stack to the circuit. Then, the control unit shuts off the reactant flow and opens the purge control valve for a selected period of time. [0015]
  • The purge system may further include a pressure regulator connected to the purge conduit and communicative with the control unit, to enable regulation of the pressure of purge fluid supplied to at least one of the reactant passages. [0016]
  • A suitable purge fluid is an inert gas, such as nitrogen. “Inert” in this sense means a fluid that is substantially non-reactive in the fuel cell. [0017]
  • According to another aspect of the invention, an electric power generation system is provided that has a humidifier bypass system. Such an electric power generation system comprises a fuel cell stack connectable to an external electrical circuit; when connected, the stack may supply electric current to the external circuit. The stack comprises at least one solid polymer fuel cell, reactant stream passages for directing reactant streams through at least one of the fuel cells, a humidifier in fluid communication with at least one of the reactant stream passages for humidifying a reactant stream supplied to the fuel cell stack, and a humidifier bypass system. The humidifier bypass system comprises at least one bypass conduit for transmitting at least one reactant from a reactant supply to the stack in fluid isolation from the humidifier, and a bypass control device for selectively directing flow of the reactant streams to the fuel cell stack through the humidifier or the humidifier bypass conduit. [0018]
  • Each bypass conduit typically includes an inlet end that is connected to one of the reactant stream passages upstream of the humidifier or directly to one of the reactant supplies, and an outlet end that is connected to one of the reactant stream inlet passages downstream of said humidifier and upstream of the stack. [0019]
  • The control device is operable to direct reactant fluid through the humidifier and to the stack during normal operation, that is, while electrical power is being generated by the stack, and through the bypass conduit and to the stack during a shut down procedure (for example, after supply of electric current from the stack to the external circuit has been interrupted). The control device may include at least one bypass inlet valve connected to one of the reactant passages upstream of the humidifier, and at least one bypass outlet valve connected to the same reactant passage downstream of the humidifier. The bypass conduit connects the bypass inlet and outlet valves so that reactant fluid can be transmitted in fluid isolation from the humidifier directly to the stack. The bypass control device preferably further includes a control unit communicative with the bypass inlet and outlet valves and with an input signal source. The control unit may be a micro-controller or other similar device. [0020]
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • FIG. 1 is an exploded side view of a typical solid polymer electrochemical fuel cell with a membrane electrode assembly interposed between two fluid flow field plates. [0021]
  • FIG. 2 is a perspective cut-away view of an electrochemical fuel cell stack. [0022]
  • FIG. 3 is a schematic diagram of a fuel cell electric power generation system incorporating a nitrogen gas purge system. [0023]
  • FIG. 4 is a schematic diagram of a fuel cell electric power generation system incorporating a humidifier bypass purge system. [0024]
  • FIG. 5 is a composite plot of fuel cell stack voltage versus time in minutes (plot A) and fuel cell stack core temperature versus time in minutes (plot B) for a 10-cell stack, operation of which was commenced after the stack had equilibrated at a core temperature of −11° C. [0025]
  • FIG. 6 is a composite plot of fuel cell stack voltage versus time in minutes (plot C) and fuel cell stack core temperature versus time in minutes (plot D) for a 4 cell stack, operation of which was commenced at a core temperature of −19° C. [0026]
  • FIG. 7 is a plot of voltage as a function of current density for a fuel cell containing a membrane electrode assembly with a DowPont™ membrane exposed to three cold purge freeze/thaw cycles. [0027]
  • FIG. 8 is a plot of voltage as a function of current density for the fuel cell containing a membrane electrode assembly with a Nafion® 1135 membrane exposed to three cold purge freeze/thaw cycles. [0028]
  • FIG. 9 is a plot of voltage as a function of current density for a fuel cell containing a membrane electrode assembly with a Nafion® 1135 membrane exposed to one shorter duration cold purge freeze/thaw cycle. [0029]
  • FIG. 10 is a plot of voltage as a function of current density for a fuel cell containing a membrane electrode assembly with a DowPont™ membrane exposed to three hot purge freeze/thaw cycles. [0030]
  • FIG. 11 is a plot of voltage as a function of current density for the fuel cell containing a membrane electrode assembly with a Nafion® 1135 membrane exposed to three hot purge freeze/thaw cycles. [0031]
  • FIG. 12 is a plot of cell voltage, for the fuel cell containing a membrane electrode assembly with a [0032] Nafion® 112 membrane, after each of a series of 55 cold purge freeze/thaw cycles.
  • FIG. 13 is a plot of stack voltage against operating time for an 8-cell Ballard Mark 513 fuel cell stack which was subjected to a series of freeze-thaw-operation cycles, interspersed with four heat treatment cycles. [0033]
  • FIG. 14 is a plot of stack voltage against current density for the fuel cell stack used to generate the data of FIG. 12, before and after heat treatment[0034]
  • DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
  • FIG. 1 illustrates a [0035] typical fuel cell 10. Fuel cell 10 includes a membrane electrode assembly 12 interposed between anode flow field plate 14 and cathode flow field plate 16. Membrane electrode assembly 12 consists of an ion exchange membrane 20 interposed between two electrodes, namely, anode 21 and cathode 22. In conventional fuel cells, anode 21 and cathode 22 comprise a substrate of porous electrically conductive sheet material 23 and 24, respectively, for example, carbon fiber paper or carbon cloth. Each substrate has a thin layer of electrocatalyst 25 and 26, respectively, disposed on one surface thereof at the interface with membrane 20 to render each electrode electrochemically active.
  • As further shown in FIG. 1, anode [0036] flow field plate 14 has at least one fuel flow channel 14 a formed in its surface facing anode 21. Similarly, cathode separator plate 16 has at least one oxidant flow channel 16 a formed in its surface facing cathode 22. When assembled against the cooperating surfaces of electrodes 21 and 22, channels 14 a and 16 a form the reactant flow field passages for the fuel and oxidant, respectively. The flow field plates are electrically conductive.
  • Turning now to FIG. 2, a [0037] fuel cell stack 100 includes a plurality of fuel cell assemblies, a series of which is designated as 111 in FIG. 2. Each of the fuel cell assemblies includes a membrane electrode assembly 112 interposed between a pair of fluid flow field plates 114, 116. Fuel cell stack 100 also includes a first end plate 130 and a second end plate 140.
  • [0038] Plate 130 includes fluid inlet ports 132, 134, 136 for introducing fluid fuel, oxidant and coolant streams, respectively, to the stack. Plate 140 includes fluid outlet ports 142, 144, 146 for exhausting fluid fuel, oxidant and coolant streams, respectively, from the stack. The fluid outlet ports are fluidly connected to the corresponding fluid inlet ports via passages within the stack.
  • The fuel cell assemblies have a series of openings formed therein, which cooperate with corresponding openings in adjacent assemblies to form [0039] fluid manifolds 152, 154, 156, 162, 164, 166 within the stack 100. The fluid manifolds are each circumscribed by a sealant material or gasket. In addition, a peripheral seal at the exterior perimeter of each fuel cell fluidly isolates the interior, electrochemically active portion of the fuel cell from the external environment.
  • A fuel stream entering the stack via [0040] fuel inlet port 132 is directed to the individual fuel flow field plates via manifold 152. After passing through the fuel flow field plate channels, the fuel stream is collected in manifold 162 and exhausted from the stack via fuel outlet port 142. Similarly, an oxidant stream entering the stack via oxidant inlet port 134 is directed to individual oxidant flow field plates via manifold 154. After passing through the oxidant flow field plate channels, the oxidant stream is collected in manifold 164 and exhausted from the stack via oxidant outlet port 144. A fluid coolant (typically water) introduced via coolant inlet port 136 is directed to coolant plate assemblies (not shown) in the stack 100 via manifold 156. The coolant stream is collected in manifold 166 and exhausted from the stack via coolant outlet port 146. Coolant manifolds 156, 166 may be fitted with a compliant mechanism (not shown), such as tube cushions or inserts made of closed cell foam, to accommodate the expansion of freezing water. Tie rods 170 extend between end plates 130 and 140 to compress and secure stack 100 in its assembled state with fastening nuts 172 disposed at opposite ends of each tie rod, and disc springs 174 interposed between the fastening nuts 172 and end plates 130, 140.
  • FIG. 3 is a schematic diagram of a fuel cell electric [0041] power generation system 200 comprising a fuel cell stack 210 and a nitrogen gas purge system 250. The fuel cell stack 210 includes negative and positive bus plates 212, 214, respectively, to which an external circuit comprising a variable load 216 is electrically connectable to the stack 210 by closing switch 218. The system includes a fuel (hydrogen) circuit, an oxidant (air) circuit, and a coolant water circuit. The reactant and coolant streams are circulated in the system 200 in various conduits illustrated schematically in FIG. 3.
  • A [0042] hydrogen supply 220 is connected to the stack 210; hydrogen pressure is controllable by pressure regulator 221. Water in the hydrogen stream exiting the stack 210 is accumulated in a knock drum 222, which can be drained by opening valve 223. Unreacted hydrogen is recirculated to stack 210 by a pump 224 in recirculation loop 225. An air supply 230 is connected to the stack 210, the pressure of which is controllable by pressure regulator 231. Water in the air stream exiting the stack 210 is accumulated in reservoir 232, which can be drained by opening valve 233, and the air stream is vented from the system via valve 234.
  • In the [0043] coolant water loop 240, water is pumped from reservoir 232 and circulated through stack 210 by pump 241. The temperature of the water is adjusted in a heat exchanger 242.
  • [0044] Purge system 250 is used to purge the hydrogen and oxidant passages in fuel cell stack 210 with a low humidity, non-reactive gas such as nitrogen. Flow of purge gas from a purge gas supply 260 to the hydrogen and air inlet passages 261, 262 is transmitted through purge supply conduits 268, 269 and three way valves 266, 267 connected to respective hydrogen and air inlet passages 261, 262 upstream of the stack 210. The flow of nitrogen through each purge conduit 268, 269 is controlled by respective flow regulating valves 263, 264.
  • A micro-controller (not shown) or similar electronic control unit may be provided to automate at least some of the purge system operation. In a simple set-up, the microcontroller is programmed to control [0045] valves 221, 231, 263, 264, 265 266, 267, and switch 218. Upon receipt of instructions to shut down the system, the micro-controller opens switch 218 to interrupt the flow of electricity from the stack 210 to the circuit, then closes air and hydrogen supply valves 221, 231 and opens valves 263, 264, 266, 267 to enable purge fluid to be transmitted through conduits 268, 269 to air and hydrogen conduits 261, 262 and through the stack 210.
  • An additional purge conduit and three way valve (both not shown) may be connected to the coolant loop upstream of the [0046] stack 210 to enable purging of the coolant loop during the shut down procedure. The micro-controller is adapted accordingly to shut down pump 241 and heat exchanger 242 prior to directing purge fluid to the coolant loop.
  • Alternatively, the reactant streams themselves can be employed as the purge streams. Preferably the purge fluid, if it is a gas, is dry or at least not humidified. Thus, when employing the reactant streams as the purge streams, reactant stream humidifiers (if any) are bypassed to provide streams having water carrying capacity greater than humidified reactant streams. Referring to FIG. 4, a humidifier [0047] bypass purge system 300 replaces the nitrogen gas purge system 250 and comprises a series of valves and conduits that cooperate to direct the supply oxidant and fuel streams in fluid isolation from a humidifier. Particularly, upstream three- way bypass valves 302, 304 are provided on respective fuel and oxidant inlet passages 261, 262 between the oxidant and fuel supply sources 220, 230, and a humidifier 306. The humidifier 306 is preferably a contact-type gas humidifier; however other types of humidifiers known to a person skilled in the art can be used, for example, a membrane humidifier. A fuel bypass conduit 308 is connected to upstream fuel bypass valve 302 and to a downstream three-way valve 267 connected to fuel inlet passage 261 downstream of humidifier 306 and upstream of stack 210. Similarly, an oxidant bypass conduit 310 is connected to upstream oxidant bypass valve 304 and to a downstream three-way valve 266 connected to the oxidant inlet passage 262 downstream of the humidifier 306 and upstream of stack 210. The respective oxidant and fuel upstream and downstream bypass valves 302, 304, 267, 266 are operated to direct reactant flow through humidifier 306 and to stack 210 during normal stack operation, and through bypass conduits 308, 310 to stack 210 during a purging operation. As the bypass conduits 308, 310 are in fluid isolation from the humidifier 306, reactant supplied to the stack 210 via the bypass conduits 308, 310 avoid humidification. A control device (not shown ) similar to that used to control the purge system 250 may be programmed to control the humidification bypass operation.
  • FIG. 5 is a composite plot of fuel cell stack voltage versus time in minutes (plot A) and fuel cell stack core temperature versus time in minutes (plot B) for a 10-cell stack to which the flow of fuel and oxidant was restored after the stack had equilibrated at a core temperature of −11° C. [0048]
  • The stack had been operating previously, and therefore the reactant flow passages contained moist gases. Before decreasing the stack core temperature below the freezing temperature of water, the reactant and coolant water passages within the stack were purged by circulating dry, compressed air through them. The stack core temperature was then lowered below the freezing temperature of water by exposing the stack to a surrounding environment with a temperature below the freezing temperature of water. For the purposes of the examples described herein, the stack was typically placed in an insulated chamber, with the fluid and electrical connections to the stack fitted through the chamber walls. Cold nitrogen gas from a liquid nitrogen source was circulated through the chamber. The stack core temperature was measured using a thermocouple positioned in a thermally conductive plate located between two fuel cells in the center of the stack. Stack voltage, stack current and ambient temperature were also monitored. [0049]
  • When circulation of hydrogen and air through the stack was commenced at a stack core temperature of −11° C. (at time=0 minutes), the open circuit voltage was normal. A load (360 amp) was connected in the circuit after approximately three minutes, causing the stack core temperature to rise rapidly while the voltage decreased but recovered gradually. Once operation of the stack had commenced, the exothermic reaction of hydrogen and oxygen within the stack and the resistive heating due to internal ohmic losses caused the stack core temperature to rise. [0050]
  • FIG. 6 is a composite plot of fuel cell stack voltage versus time in minutes (plot C) and fuel cell stack core temperature versus time in minutes (plot D) for a 4-cell stack, operation of which was commenced at a core temperature of −19° C. [0051]
  • Again, as the stack had been operating previously, before decreasing the stack core temperature to −19° C., the reactant passages within the stack were purged by circulating dry nitrogen. Coolant water remained in the coolant passages. Preferably the purge fluid is an inert gas such as nitrogen. Circulation of hydrogen and air was commenced with a load (50 amp) connected. Approximately 2 minutes transpired before the output current reached 50 amps. The load was increased to 260 amps once the stack reached about 30° C., and the coolant pump was then activated. One cell in the stack was not operating properly; hence the lower than normal average cell voltages. [0052]
  • During commencement of stack operation, it has been found advantageous to refrain from circulating the fluid coolant stream within the stack until the stack has reached a temperature above the freezing temperature of water. More preferably, the fluid coolant stream is not circulated until the stack has reached a temperature at or near the desired stack operating temperature. In this regard, the circulating fluid coolant stream, assuming it is not preheated, will absorb and carry away heat otherwise available to warm the stack. Refraining from circulating the fluid coolant stream therefore expedites the warming of the stack to its desired operating temperature. [0053]
  • The cold start capability and freeze tolerance of fuel cells can be improved by reducing the amount of water remaining within the passages of the stack upon cessation of operation and reduction of stack core temperature to near or below the freezing temperature of water. As used herein, “freeze tolerance” refers to the ability of a fuel cell or fuel cell stack to maintain substantially the same performance after one or more freeze/thaw cycles. [0054]
  • The reactant passages, including the manifolds and individual fuel cell reactant flow passages within a fuel cell stack, are preferably purged with a fluid stream before the temperature of the stack is decreased to below the freezing temperature of water. Preferably a fluid which is not reactive in the fuel cell environment, such as nitrogen gas, is used. A liquid may be used as the purge fluid. Preferably it would be a liquid that does not freeze at the temperature to which the fuel cell is to be exposed, and which has no detrimental effect on the fuel cell components. [0055]
  • The greater water carrying capacity of unhumidified reactant purge streams will result in more effective absorption and removal of water from the reactant stream conduits and porous components of the stack. Although all the reactant and coolant passages may be desirably purged in some situations, it has also been found effective in many cases to purge the oxidant stream passages only. This can simplify the system and the shutdown sequence. [0056]
  • It has been found that improved cold start capability and freeze tolerance of fuel cells to multiple freeze/thaw cycles can also be achieved when one or more of the fuel, oxidant, coolant and humidification passages are purged after the stack core temperature has been reduced to at or below normal room temperature (hereinafter referred to as “cold purging”). The beneficial effect of purging is not quite so pronounced when the stack passages are purged at a temperature within the normal stack operating temperature range (hereinafter referred to as “hot purging”). [0057]
  • EXAMPLES—PURGE METHODS
  • Experimental Details [0058]
  • The effect of cold and hot purging on membrane electrode assemblies having two different membrane types, Nafion® 1135 and a DowPont™ membrane, in a Ballard Mark 513 single fuel cell with an internal humidifier was investigated. Separate water feed lines for the coolant and humidification streams were employed. The coolant outlet temperature was 85° C. with a ΔT (change in temperature from inlet to outlet) of 10° C. at 1000 amps per square foot (ASF) (10764 amps per square foot (ASM)), using air as the oxidant. Both MEAs had a screen printed anode containing 3.87 mg/cm[0059] 2 platinum black electrocatalyst on carbon fiber paper. For the cathode, both MEAs had 3.87 mg/cm2 platinum black electrocatalyst applied by hand to carbon fiber paper. The Nafion® 1135 membrane employed in MEA No. 513-15 had an equivalent weight of 1100 and a thickness of about 85 μm (dry). The DowPont™ membrane employed in MEA No. 513-22 had an equivalent weight of 800 and a thickness of about 100 μm (wet).
  • The Mark 513 cell was assembled and run overnight at 600 ASF (6458 ASM) at an air/fuel pressure of 30/30 psig (207/207 kPa gauge) and a stoichiometry of 2/1.5 respectively. The fuel was substantially pure hydrogen. “Stoichiometry” is the ratio of the amount of reactant supplied to the fuel cell stack to the amount of reactant actually consumed in the fuel cell stack. In this instance, a fuel stoichiometry of 1.5 means that 150 parts of hydrogen are supplied to the fuel cell for each 100 parts actually consumed in the fuel cell. [0060]
  • Cold Purge Freeze/Thaw Cycles [0061]
  • For the initial series of three freeze/thaw cycles (results shown in FIGS. 7 and 8), the cell was cooled from its normal operating temperature (approximately 85° C.) to room temperature (approximately 23° C.) before purging. In each case, the fuel, oxidant, coolant and humidification passages were purged for approximately 7 minutes with nitrogen. The cell containing the Nafion® 1135 membrane was taken through a fourth freeze/thaw cycle with a purge duration of only approximately 1 minute (results shown in FIG. 8). The cell inlets and outlets were capped and the cell was placed in a freezer. Internal sealing pressure within the cell was maintained during freezing. The freezer temperature was approximately −20° C. The duration of the freeze ranged from 15-20 hours. After removal from the freezer, the coolant lines were connected and the cell was heated to 50° C. At that point, operation of the fuel cell was commenced at 50 ASF (538.2 ASM) with excess fuel and oxidant flow rates. When the cell temperature reached 60° C., the current density was increased to 600 ASF (6458 ASM) and the cell was operated for at least one hour or until cell voltage had stabilized. A polarization test from 0 to 1000 ASF (0 to 10764 ASM) was performed for each of the two MEAs tested, using two different oxidant streams: air and substantially pure oxygen. [0062]
  • FIG. 7 is a plot of voltage as a function of current density for the fuel cell containing MEA 513-22 (DowPont™ membrane). Plots [0063] 1-4 show the performance on air prior to freezing (which is the plot with the solid line and solid data points ♦), and after each of the three cold purge freeze/thaw cycles described above. Plots 5-8 show the performance on oxygen prior to freezing (which is the plot with the solid line and solid data points ▴), and after each of the three cold purge freeze/thaw cycles described above. For each of the oxidant streams, the four plots in FIG. 7 are difficult to distinguish from one another.
  • FIG. 8 is a plot of voltage as a function of current density for the fuel cell containing MEA 513-12 (Nafion® 1135 membrane). Plots [0064] 1-4 show the performance on air prior to freezing (which is the plot with the solid line and solid data points ♦), and after each of the three cold purge freeze/thaw cycles described above. Plots 5-8 show the performance on oxygen prior to freezing (which is the plot with the solid line and solid data points ▴), and after each of the three cold purge freeze/thaw cycles described above. Again, for each of the oxidant streams, the four plots in FIG. 8 are difficult to distinguish from one another.
  • FIG. 9 is a plot of voltage as a function of current density for the fuel cell containing MEA 513-12 (Nafion® 1135 membrane). Plots [0065] 1-2 show the performance on air prior to freezing (which is the plot with the solid line and solid data points ♦), and after the fourth cold purge freeze/thaw cycle described above, in which a shorter purge duration (approximately 1 minute) was used. Plots 3-4 show the performance on oxygen prior to freezing (which is the plot with the solid line and solid data points ▴) and after the fourth cold purge freeze/thaw cycle described above. Again, for each of the oxidant streams, the two plots in FIG. 8 are difficult to distinguish from one another, indicating that a shorter duration purge can give satisfactory results.
  • Thus, based on the results shown in FIGS. 7, 8 and [0066] 9 for both MEAs, substantially no mass transport losses were exhibited over the series of three or four freeze/thaw cycles. The performance after each freeze/thaw cycle was maintained at approximately baseline (prior to freezing) polarization levels. Both MEAs thus exhibited favorable freeze/thaw tolerance when the cold purging technique was used.
  • Hot Purge Freeze/Thaw Cycles [0067]
  • For a subsequent series of three freeze/thaw cycles, each cell was purged at stack operating temperature (approximately 85° C.) before cooling. The fuel, oxidant, coolant and humidification passages were purged for approximately 1 minute with nitrogen. The cell inlets and outlets were capped and the cell was placed in a freezer. Internal sealing pressure within the cell was maintained during freezing. The freezer temperature was approximately −20° C. The duration of the freeze ranged from 15-20 hours. After removal from the freezer, the coolant lines were connected and the cell was heated to operating temperature and operation commenced using essentially the same procedure employed for the cold purge freeze/thaw cycles described above. A polarization test from 0 to 1000 ASF (0 to 10764 ASM) was performed for each of the two MEAs tested, again using two different oxidant streams: air and substantially pure oxygen. [0068]
  • FIG. 10 is a plot of voltage as a function of current density for the fuel cell containing MEA 513-22 (DowPont™ membrane). Plots [0069] 1-4 show the performance on air prior to freezing (which is the plot with the solid line and solid data points ♦), and after each of the three hot purge freeze/thaw cycles described above. Plots 5-8 show the performance on oxygen prior to freezing (which is the plot with the solid line and solid data points ▴), and after each of the three hot purge freeze/thaw cycles described above. A significant mass transport effect appears to occur at higher current densities on air after the third freeze cycle, based on the increased difference between the air and oxygen performance levels.
  • FIG. 11 is a plot of voltage as a function of current density for the fuel cell containing MEA 513-12 (Nafion® 1135 membrane. Plots [0070] 1-4 show the performance on air prior to freezing (which is the plot with the solid line and solid data points ♦), and after each of the three hot purge freeze/thaw cycles described above. Plots 5-8 show the performance on oxygen prior to freezing (which is the plot with the solid line and solid data points ▴), and after each of the three hot purge freeze/thaw cycles described above. Again, a significant mass transport effect appears to occur at higher current densities on air, based on the progressively increasing difference between the air and oxygen performance levels after each freeze/thaw cycle.
  • The particularly favorable results obtained with the cold purge technique were further supported by the following test in which a single fuel cell was cycled through 55 freeze/thaw cycles, with the purge technique used on the coolant and cathode side passages only. [0071]
  • Experimental Details [0072]
  • The effect of repeated cold purging on a membrane electrode assembly having a [0073] Nafion® 112 membrane, in a Ballard Mark 513 single fuel cell with an external humidifier was investigated. Separate water feed lines for the coolant and humidification streams were employed. The coolant inlet temperature was 70° C. with a ΔT (change in temperature from inlet to outlet) of 15° C. at 1 A/cm2 using air as the oxidant. The MEA had a screen printed anode containing 0.34-0.38 mg/cm2 platinum black electrocatalyst and a screen printed cathode containing 0.73-0.82 mg/cm2 platinum black electrocatalyst on carbon fiber paper, both with a Nafion spray coating (0.2 mg/cm2).
  • The cell was tested in a temperature-controlled environmental chamber at an air/fuel pressure of 27/27 psig (186/186 kPa gauge) and a stoichiometry of 1.8/1.2 respectively. The fuel was a simulated methanol reformate stream (composition 63.5% hydrogen; 22.5% carbon dioxide; 13% nitrogen; 1% methanol and 40 parts per million (ppm) carbon monoxide), and a 4% air bleed was employed at the anode. The fuel and oxidant streams were humidified. [0074]
  • For the series of 55 freeze/thaw cycles (results shown in FIG. 12), the cell was cooled from its normal operating temperature (approximately 80° C.) to a chamber temperature at which no part of the stack was below 0° C., but where the cell temperature was approximately 30° C. before purging. In each case, the oxidant passages were purged for approximately 10 seconds with dry (unhumidified) air. The cell inlets and outlets were closed by actuated valves, and the temperature in the chamber was reduced to approximately −25° C. The duration of each freeze was approximately 1 hour. Internal sealing pressure within the cell was maintained during freezing. The cell was then thawed to 5° C. and then heated, by circulating warm coolant, to 65° C. At that point, operation of the fuel cell was commenced at 0.5 A/cm[0075] 2 for 60 minutes, then at 1.0 A/cm2 for 30 minutes, then for a second time at 0.5 A/cm2 for 30 minutes.
  • FIG. 12 shows the results obtained after each of 55 such cycles with the cell voltage measured once it had stabilized at 1.0 A/cm[0076] 2 during the 30 minutes of operation at that current density (Plot A) and once it had stabilized at 0.5 A/cm2 during the second period of operation at that current density (Plot B). At both current densities the performance degradation over the 55 cycles was negligible: approximately −0.1 mV/cycle at 0.5 A/cm2 and approximately −0.2 mV/cycle at 1.0 A/cm2.
  • EXAMPLES—HEAT TREATMENT METHODS
  • FIG. 13 shows a plot of stack voltage against operating time for an 8-cell Ballard Mark 513 fuel cell stack which was subjected to a series of freeze-thaw-operation cycles. Prior to freezing the fuel, oxidant and coolant passages were purged with dry gas. During the freezing cycles, the cell inlets and outlets were capped and the cell was placed in a freezer. Internal sealing pressure within the cell was maintained during freezing. The freezer temperature was approximately −20° C. The duration of the freeze in each case was greater than 12 hours. After some cycles the stack was operated normally, and after other cycles the stack operating temperature was increased to above its normal operating temperature for a period, before normal operation was resumed. The stack was operated on humidified air and hydrogen, both at 30 psig (207 kPa gauge), at stoichiometries of 2.0 and 1.5 respectively, at a current density of 700 ASF (7535 ASM) to generate the data shown in FIG. 12. The coolant inlet temperature was 75° C. with a ΔT (change in temperature from inlet to outlet) of 10° C. at 1000 ASF (10764 ASM). [0077]
  • Referring to FIG. 13, between 425 and 882 hours the stack was operated, frozen several times, and then started up having been warmed to 50° C. Data points obtained directly after a freeze cycle are marked “F”. It can be seen that the cell performance deteriorated after each freeze cycle. After 882 hours the stack was started up after freeze cycles having been warmed to only 10° C. After 950 hours the stack was started up after freeze cycles having been warmed to only 0° C. The performance losses observed did not appear to be significantly affected by the start temperature. [0078]
  • A substantial improvement in performance after freezing was obtained in 4 cases where stack operation was commenced and then the stack operating temperature was increased to above the normal stack operating temperature of about 85° C., namely, to approximately 100° C. Data points obtained directly after such heat treatments are marked “H”. [0079]
  • FIG. 14 shows a plot of stack voltage as a function of current density for the 8-cell Ballard Mark 513 fuel cell stack used to generate the data of FIG. 13. Plots A, B and C show performance curves for operation on air, and plots D, E and F for operation on oxygen. Plots A and D show the stack performance before any of the heat treatments referred to the description of FIG. 13 but after the final freeze cycle, plots B and E show the stack performance immediately after the fourth heat treatment, and plots C and F show the stack performance about 2 days after the fourth heat treatment. The results on air show a substantial and sustained improvement in post-freezing performance after the heat treatment. The improvement is believed to be attributable to improved mass transport in the MEA, based on the fact that on oxygen the performance was not significantly affected by the heat treatment. This indicates that performance loss after freezing may be, at least in part, due to mass transport difficulties in the cells, which have a more significant effect on air than on a substantially pure oxidant stream. These detrimental effects could be due to retained water in the membrane electrode assembly. It is possible that the heat treatment method assists in removing residual water from the membrane electrode assembly, and thereby improves performance at start-up, particularly on air. [0080]
  • While particular elements, embodiments and applications of the present invention have been shown and described, it will be understood, of course, that the invention is not limited thereto since modifications may be made by those skilled in the art without departing from the scope of the present disclosure, particularly in light of the foregoing teachings [0081]

Claims (22)

What is claimed is:
1. An electric power generation system comprising
(a) a fuel cell stack connectable to an external electrical circuit for supplying electric current to said external circuit, said stack comprising at least one solid polymer fuel cell and fluid stream passages for directing fluid streams through said at least one fuel cell; and
(b) a purge system comprising a purge conduit having an inlet end connectable to a purge fluid supply and an outlet end connected to at least one of said fluid stream passages, and a purge flow control device for controlling the flow of a pressurized purge fluid through said purge conduit such that water is capable of being purged from at least one of said fluid stream passages after a supply of electric current from said stack to said external circuit has been interrupted.
2. The electric power generation system of
claim 1
wherein said fluid stream passages are reactant stream passages.
3. The electric power generation system of
claim 2
wherein said reactant stream passages comprise oxidant stream passages.
4. The electric power generation system of
claim 2
wherein said reactant stream passages comprise fuel stream passages.
5. The electric power generation system of
claim 1
wherein said fluid stream passages comprise a coolant passage.
6. The electric power generation system of
claim 1
wherein said purge flow control device comprises a control valve connected to said purge conduit.
7. The electric power generation system of
claim 6
wherein said purge flow control device further comprises a control unit communicative with said control valve and with an input signal source.
8. The electric power generation system of
claim 7
wherein said control unit is a microcontroller.
9. The electric power generation system of
claim 1
wherein said purge system further comprises a pressure regulator associated with said purge conduit for regulating the pressure of said purge fluid from said purge fluid supply to said at least one reactant passage.
10. The electric power generation system of
claim 1
wherein said purge fluid is inert.
11. The electric power generation system of
claim 11
wherein said purge fluid is nitrogen.
12. An electric power generation system comprising:
(a) a fuel cell stack connectable to an external electrical circuit for supplying electric current to said external circuit, said stack comprising at least one solid polymer fuel cell, and reactant stream passages for directing reactant streams through said at least one fuel cell; and
(b) a humidifier in fluid communication with at least one of said reactant stream passages, for humidifying a reactant stream supplied to said fuel cell stack; and
(c) a humidifier bypass system comprising at least one bypass conduit for directing said reactant stream to said stack in fluid isolation from said humidifier and a bypass control device for selectively directing flow of said reactant stream to said fuel cell stack through either of said humidifier and said humidifier bypass conduit.
13. The electric power generation system of
claim 12
wherein said at least one bypass conduit comprises an inlet end connected to one of said reactant stream passages upstream of said humidifier, and an outlet end connected to one of said reactant stream passages downstream of said humidifier.
14. The electric power generation system of
claim 12
wherein said at least one bypass conduit comprises an inlet end connectable to a reactant supply, and an outlet end connected to one of said reactant stream passages downstream of said humidifier.
15. The electric power generation system of
claim 12
wherein said control device is operable such that said reactant fluid is directed to said humidifier while electrical power is being generated by the stack and to said bypass conduit after a supply of electric current from said stack to said external circuit has been interrupted.
16. The electric power generation system of
claim 15
wherein said bypass control device comprises a bypass inlet valve connected to one of said reactant passages upstream of said humidifier, and a bypass outlet valve connected to one of said reactant passages downstream of said humidifier, and wherein said bypass conduit is connected to said bypass inlet and outlet valves.
17. The electric power generation system of
claim 16
wherein said bypass control device further comprises a control unit communicative with said bypass inlet and outlet valves and with an input signal source.
18. The electric power generation system of
claim 18
wherein said control unit is a microcontroller.
19. The electric power generation system of
claim 12
wherein one of said reactant passages is an oxidant flow passage.
20. The electric power generation system of
claim 12
wherein one of said reactant passages is a fuel flow passage.
21. An electric power generation system comprising
(a) a fuel cell stack connectable to an external electrical circuit for supplying electric current to said external circuit, said stack comprising at least one solid polymer fuel cell, and fluid stream passages for directing fluid streams through said at least one fuel cell; and
(b) a mechanism for directing the flow of a pressurized purge fluid from a purge fluid supply to at least one of said fluid stream passages such that water can be purged from said at least one purged fluid stream passage after a supply of electric current from said stack to said external circuit has been interrupted.
22. An electric power generation system comprising
(a) a fuel cell stack connectable to an external electrical circuit for supplying electric current to said external circuit, said stack comprising at least one solid polymer fuel cell, and reactant stream passages for directing reactant streams through said at least one fuel cell;
(b) apparatus for humidifying at least one of said reactant streams supplied to said fuel cell stack; and
(c) a humidifier bypass system comprising apparatus for directing at least one of said reactant streams to said stack in fluid isolation from said humidifying apparatus, and apparatus for selectively directing flow of said reactant streams to said fuel cell stack through said humidifying apparatus or in fluid isolation from said humidifying apparatus.
US09/819,875 1996-06-07 2001-03-28 Apparatus for improving the cold starting capability of an electrochemical fuel cell Abandoned US20010055707A1 (en)

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US09/819,506 Pending US20020009623A1 (en) 1999-09-27 2001-03-28 Methods and apparatus for improving the cold starting capability of a fuel cell
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