[go: up one dir, main page]

US20090053568A1 - Evaporative Cooling of Fuel Cells Employing Antifreeze Solution - Google Patents

Evaporative Cooling of Fuel Cells Employing Antifreeze Solution Download PDF

Info

Publication number
US20090053568A1
US20090053568A1 US12/086,468 US8646808A US2009053568A1 US 20090053568 A1 US20090053568 A1 US 20090053568A1 US 8646808 A US8646808 A US 8646808A US 2009053568 A1 US2009053568 A1 US 2009053568A1
Authority
US
United States
Prior art keywords
coolant
water
reservoir
channels
power plant
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US12/086,468
Inventor
Jeremy P. Meyers
Ryan J. Balliet
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
UTC Power Corp
Original Assignee
UTC Fuel Cells LLC
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by UTC Fuel Cells LLC filed Critical UTC Fuel Cells LLC
Assigned to UTC FUEL CELLS, LLC reassignment UTC FUEL CELLS, LLC ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: BALLIET, RAYAN J., MEYERS, JEREMY P.
Publication of US20090053568A1 publication Critical patent/US20090053568A1/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B60VEHICLES IN GENERAL
    • B60CVEHICLE TYRES; TYRE INFLATION; TYRE CHANGING; CONNECTING VALVES TO INFLATABLE ELASTIC BODIES IN GENERAL; DEVICES OR ARRANGEMENTS RELATED TO TYRES
    • B60C1/00Tyres characterised by the chemical composition or the physical arrangement or mixture of the composition
    • B60C1/0016Compositions of the tread
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L15/00Compositions of rubber derivatives
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L7/00Compositions of natural rubber
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08CTREATMENT OR CHEMICAL MODIFICATION OF RUBBERS
    • C08C19/00Chemical modification of rubber
    • C08C19/04Oxidation
    • C08C19/06Epoxidation
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/02Elements
    • C08K3/04Carbon
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/34Silicon-containing compounds
    • C08K3/36Silica
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/54Silicon-containing compounds
    • C08K5/548Silicon-containing compounds containing sulfur
    • 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
    • Y02TCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO TRANSPORTATION
    • Y02T10/00Road transport of goods or passengers
    • Y02T10/80Technologies aiming to reduce greenhouse gasses emissions common to all road transportation technologies
    • Y02T10/86Optimisation of rolling resistance, e.g. weight reduction 

Definitions

  • This invention relates to circulating an antifreeze solution from a reservoir through water channels of porous, hydrophilic water transport plates and back to the reservoir; the mixture enters the fine pores of the water transport plates which are warmed by the heat of the fuel cell process, thereby evaporating water which may include product water (but not antifreeze) from the plates into the process oxidant flow channels, cooling the fuel cells. Water is condensed out of the process air oxidant exhaust and returned to re-mix with the concentrated antifreeze.
  • fuel cells in a fuel cell power plant are evaporatively cooled by evaporation of at least some of the water in an antifreeze mixture with a freeze depressing substance in the porous, hydrophilic reactant gas flow field plates, which typically have reactant gas flow channels extending from a surface of reactant flow field plates opposite from coolant passageways.
  • the antifreeze coolant mixture circulates through the coolant passageways in or adjacent the reactant gas flow field plates. A more concentrated mixture returns to a coolant reservoir.
  • the evaporation of water from the antifreeze mixture and product water into the reactant streams (primarily the cathode) cools the fuel cell stack.
  • At least some water vapor is condensed out of at least the oxidant reactant gas stream exiting from the stack, the condensed water being returned to the mixture in the accumulator.
  • less than all of the water vapor in the air exhaust may be condensed.
  • the rate of condensing may be controlled using a condensate controller to ensure proper water balance, such as a variable flow cooling fan for the condenser, or by cooling the air in the condenser with a controlled circulation of antifreeze.
  • FIG. 1 is a block illustration of the invention.
  • FIG. 2 is a partial perspective view of an embodiment of the invention.
  • FIG. 3 is a fragmentary view of a variation of FIG. 1 .
  • FIG. 4 is a fragmentary view of an alternative to the embodiment of FIG. 2 .
  • FIG. 5 is a sectioned, side elevation view, with sectioning lines omitted for clarity, of portions of fuel cells useful with the invention.
  • a fuel cell power plant 19 has a stack 20 of fuel cells.
  • the concept of the present invention is illustrated by the density of stippling to provide a rough indication of the fraction of fluid in the fuel cell stack coolant that is antifreeze 23 , such as polyethylene glycol (PEG) or other non-volatile, miscible fluid that sufficiently suppresses the freezing point of a mixture with water.
  • PEG polyethylene glycol
  • FIG. 1 PEG and water are mixed in a reservoir 21 , assisted by a pump 22 , so as to achieve the desired freeze point of the mixture. Because the pump is in an antifreeze solution, the pump will not be rendered inoperable due to freezing conditions.
  • the desired mixture such as at the top 25 of the reservoir 21 , is fed through a conventional coolant inlet manifold 26 into coolant channels 28 of the fuel cells (described with respect to FIG. 4 , hereinafter) in the stack 20 , in which the coolant channels are formed within or in fluid communication with, porous, hydrophilic water transport plates 29 , which have fine pores that contain a water-antifreeze mixture.
  • the fuel cell coolant channels 28 are connected to a coolant exit manifold 32 which is interconnected by means of a conduit 33 to the reservoir 21 .
  • the coolant may be substantially antifreeze 23 (e.g., PEG); that is to say, a very concentrated solution of antifreeze 23 .
  • this is remixed in the reservoir 21 , such as by means of the pump 22 , if desired; if the pump 22 is not necessary in any given embodiment of the invention, it may be omitted.
  • other ways of assuring an adequate mixing of the returned antifreeze 23 with the rest of the fluid in the reservoir 21 may be used within the purview of the present invention.
  • the water transport plates 29 absorb heat generated in the catalytic reaction of oxygen and hydrogen.
  • the antifreeze 23 is non-volatile at the operating temperature of the fuel cell stack, on the order of 60° C.-70° C. (140° F.-158° F.)
  • water evaporates into the oxidant reactant gas stream flow channels 41 that receive oxidant, such as air from an air inlet manifold 42 , cooling the fuel cells by the heat of vaporization.
  • the condensate which is essentially pure water, flows to the reservoir 21 directly or through a conduit 48 .
  • the mixture is dilute. However, it is remixed with concentrated antifreeze 23 within the reservoir before reentering the fuel cells through the coolant inlet manifold 26 .
  • FIG. 2 illustrates a portion of the fuel cell power plant 19 including the fuel cell stack 20 , which employs evaporative cooling.
  • Air is provided to the air inlet manifold 42 and proceeds through the oxidant flow field channels 41 ( FIG. 1 ) to the air exit manifold 45 and thence into the condenser 46 .
  • the air outflow from the condenser 46 is above the water line 51 of the water reservoir 21 .
  • the cool dried air is expelled to exhaust 47 .
  • the coolant for the condenser 46 may comprise ambient air as illustrated by arrows 52 , the volume of which is controlled by a condenser controller 53 that varies the speed of a flow fan 54 in order to adjust the condensation rate as needed.
  • the condenser 46 may serve as a manifold, and the air exit manifold 45 may then be omitted.
  • Coolant from the reservoir 21 flows through a coolant conduit 60 to the coolant inlet manifold 26 .
  • the coolant passes into the coolant channels (as described with respect to FIG. 1 hereinbefore) to the top of the fuel cell stack 20 , and through the coolant exit manifold 32 .
  • Coolant flowing out of the coolant exit manifold 32 is recirculated over the conduit 33 to the reservoir 21 .
  • the water in the coolant mixture entering through coolant inlet manifold 26 replaces that which is evaporated into the process air channels 41 , as described with respect to FIG. 1 hereinbefore.
  • the pump 22 may be disposed at the inlet 37 to draw the coolant into the reservoir 21 from the line 33 as shown in FIG. 3 .
  • a pump 60 FIG. 4
  • a pump will be required in order to assure that the flow of antifreeze mixture is sufficient to provide enough water so that evaporation will occur throughout all portions of all of the fuel cells, and to prevent the antifreeze component from partially or completely filling the pores of the water transport plates.
  • the pressure drop across the coolant channels will be high, or, the coolant channels will have to be larger (deeper) to accommodate the coolant flow rates required to cool the stack. Deeper channels decrease the number of cells per unit of stack length compared to fuel cell stacks employing water transport plates and using evaporative cooling. The channel depth will nonetheless be shallower than in systems employing coolant water or similar systems employing an antifreeze mixture to cool the stack using the fluid sensible heat exchange. Thus, the invention will provide power density which is greater than traditional water or antifreeze cooling systems.
  • fuel cells 63 which may be used to implement the present invention include anode water transport plates (WTPs) 29 a having fuel reactant gas flow field channels 65 and cathode water transport plates 29 b having oxidant reactant gas (air) flow field channels 66 .
  • a membrane electrode assembly (MEA) 70 includes a proton exchange membrane with catalyst on both surfaces.
  • Gas diffusion layers (GDLs) 72 are provided adjacent each surface of the MEAs 70 .
  • the GDLs are typically constructed from carbon fiber sheet material, and are usually wettable.
  • the carbon fiber layer may or may not be wet-proofed whether a bi-layer is used or not used.
  • the invention preferably employs fuel cells 63 with GDLs 72 which are treated, such as with polytetrafluoroethylene (PTFE) to be wet-proofed, or include an additional wet-proof layer.
  • PTFE polytetrafluoroethylene
  • either the anode WTP 29 a or the cathode WTP 29 b may be solid.
  • a solid WTP will block coolant from reaching the MEA on the side it is located.
  • the cathode WTP 29 b is solid, water will reach the air (oxidant) flow field channels 66 by migration through the membranes of the MEAs 70 and GDLs 72 .
  • the surfaces of one of the WTPs 29 , adjacent to the GDL 72 including the reactant gas flow field channels 65 , 66 , may be wet-proofed by treating with a wet-proofing material, such as PTFE, to shield the membrane from the PEG or other antifreeze on that side.
  • a wet-proofing material such as PTFE
  • the coolant channels 28 may be formed by having grooves 75 on the opposite surface of the anode water transport plates 29 a from the fuel reactant gas flow field channels 65 which match up with grooves 76 on the opposite surface of cathode water transport plates 29 b from oxidant reactant gas flow field channels 66 .
  • the grooves may be in only one plate 29 a, 29 b, the matching surface of the other plate 29 b, 29 a being flat.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Tires In General (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Fuel Cell (AREA)

Abstract

A fuel cell power plant (19) has a stack of fuel cells (20) cooled by a mixture of water with a non-volatile, miscible fluid that sufficiently depresses the freezing point, such as polyethylene glycol (PEG). The water and fluid are mixed in a reservoir (21), a small pump (22, 60) flows the mixture through coolant channels (28) in or adjacent water transport plates (29); heat of the catalytic reaction warms the water transport plates causing water to evaporate therefrom thereby cooling the stack. The PEG is non-volatile at stack operating temperature and does not evaporate; concentrated PEG is returned (33) to the reservoir (21). Water in the process air flow channels (41), including evaporated process water, is recovered in a condensation-rate-controlled (53, 54)) condenser (46) in communication (48) with the reservoir (21) for remixture with the concentrated PEG solution. Hydrophobic gas diffusion layers (72) shield the proton exchange membrane (70) from the PEG.

Description

    TECHNICAL FIELD
  • This invention relates to circulating an antifreeze solution from a reservoir through water channels of porous, hydrophilic water transport plates and back to the reservoir; the mixture enters the fine pores of the water transport plates which are warmed by the heat of the fuel cell process, thereby evaporating water which may include product water (but not antifreeze) from the plates into the process oxidant flow channels, cooling the fuel cells. Water is condensed out of the process air oxidant exhaust and returned to re-mix with the concentrated antifreeze.
  • BACKGROUND ART
  • It is known that water produced at the cathodes of fuel cells has to be removed from the cathodes in order to prevent the water from blocking the flow of oxidant gas, such as air, from reaching the electrodes. It is also known that fuel cells, when operating, must be cooled to keep the fuel cells at a proper operating temperature. Some fuel cells are cooled only by conduction of heat into cooler plates which are interspersed between some or all of the fuel cells.
  • One known type of fuel cells employ reactant gas flow field plates which are porous and hydrophilic, having fine pores to allow water to pass from the cathode into the oxidant reactant gas flow channels, and to allow water to pass from the fuel reactant gas flow channels toward the membrane. These are typically called water transport plates. Cooling is typically accomplished by sensible heat transfer to water in the water flow channels formed in or adjacent to the water transport plates.
  • It has been known to cool fuel cells by evaporation, typically by providing atomized water to the reactant gas streams, which water evaporates, thereby cooling the stack.
  • In fuel cells which have employed separate cooler plates, the use of an antifreeze mixture as coolant in place of water is known. The use of separate cooler plates requires a fuel cell stack to occupy a larger volume than it would without cooler plates. Similarly, atomizing water into reactant gas streams for evaporative cooling requires additional equipment, which increases cost and volume and presents difficulty, especially at shut down, for fuel cell power plants operating in freezing environments.
  • In any of the cases referred to, even when antifreeze is used in cooler plates, the requirement to eliminate all water from the stack and auxiliary plumbing before freezing, or to otherwise accommodate the likelihood of freezing temperatures during fuel cell power plant shut down poses additional difficulties, requiring apparatus that adds cost and volume, which are most undesirable when a fuel cell is used as a power source for an electric vehicle.
  • DISCLOSURE OF INVENTION
  • Objects of the invention include: reducing the volume of a fuel cell power plant; eliminating or reducing freezable water in a fuel cell power plant system; improving fuel cell power plant for use where freezing temperatures may be encountered when the fuel cell is not operating; avoiding having freezable liquid in contact with moving parts in a fuel cell power plant; shortening fuel cell power plant startup time by reducing cell stack thermal mass; and improved fuel cell power plant.
  • According to the invention, fuel cells in a fuel cell power plant are evaporatively cooled by evaporation of at least some of the water in an antifreeze mixture with a freeze depressing substance in the porous, hydrophilic reactant gas flow field plates, which typically have reactant gas flow channels extending from a surface of reactant flow field plates opposite from coolant passageways. The antifreeze coolant mixture circulates through the coolant passageways in or adjacent the reactant gas flow field plates. A more concentrated mixture returns to a coolant reservoir. The evaporation of water from the antifreeze mixture and product water into the reactant streams (primarily the cathode) cools the fuel cell stack. At least some water vapor is condensed out of at least the oxidant reactant gas stream exiting from the stack, the condensed water being returned to the mixture in the accumulator. To avoid diluting the antifreeze mixture, less than all of the water vapor in the air exhaust may be condensed. The rate of condensing may be controlled using a condensate controller to ensure proper water balance, such as a variable flow cooling fan for the condenser, or by cooling the air in the condenser with a controlled circulation of antifreeze.
  • A pump is used to pump the antifreeze mixture in a conventional fashion similar to the manner of circulating coolant water in conventional fuel cells. Since only the antifreeze is present in the pump, freezing during shutdown is not a problem.
  • Other objects, features and advantages of the present invention will become more apparent in the light of the following detailed description of exemplary embodiments thereof, as illustrated in the accompanying drawing.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • FIG. 1 is a block illustration of the invention.
  • FIG. 2 is a partial perspective view of an embodiment of the invention.
  • FIG. 3 is a fragmentary view of a variation of FIG. 1.
  • FIG. 4 is a fragmentary view of an alternative to the embodiment of FIG. 2.
  • FIG. 5 is a sectioned, side elevation view, with sectioning lines omitted for clarity, of portions of fuel cells useful with the invention.
  • MODE(S) FOR CARRYING OUT THE INVENTION
  • Referring to FIG. 1, a fuel cell power plant 19 has a stack 20 of fuel cells. The concept of the present invention is illustrated by the density of stippling to provide a rough indication of the fraction of fluid in the fuel cell stack coolant that is antifreeze 23, such as polyethylene glycol (PEG) or other non-volatile, miscible fluid that sufficiently suppresses the freezing point of a mixture with water. In FIG. 1, PEG and water are mixed in a reservoir 21, assisted by a pump 22, so as to achieve the desired freeze point of the mixture. Because the pump is in an antifreeze solution, the pump will not be rendered inoperable due to freezing conditions.
  • The desired mixture, such as at the top 25 of the reservoir 21, is fed through a conventional coolant inlet manifold 26 into coolant channels 28 of the fuel cells (described with respect to FIG. 4, hereinafter) in the stack 20, in which the coolant channels are formed within or in fluid communication with, porous, hydrophilic water transport plates 29, which have fine pores that contain a water-antifreeze mixture.
  • The fuel cell coolant channels 28 are connected to a coolant exit manifold 32 which is interconnected by means of a conduit 33 to the reservoir 21. At the inlet 37 where the coolant returns to the reservoir, the coolant may be substantially antifreeze 23 (e.g., PEG); that is to say, a very concentrated solution of antifreeze 23. However, this is remixed in the reservoir 21, such as by means of the pump 22, if desired; if the pump 22 is not necessary in any given embodiment of the invention, it may be omitted. Furthermore, other ways of assuring an adequate mixing of the returned antifreeze 23 with the rest of the fluid in the reservoir 21 may be used within the purview of the present invention.
  • The water transport plates 29 absorb heat generated in the catalytic reaction of oxygen and hydrogen. Although the antifreeze 23 is non-volatile at the operating temperature of the fuel cell stack, on the order of 60° C.-70° C. (140° F.-158° F.), water evaporates into the oxidant reactant gas stream flow channels 41 that receive oxidant, such as air from an air inlet manifold 42, cooling the fuel cells by the heat of vaporization. The saturated (or nearly saturated) air exits the fuel cells through an air exit manifold 45 and enters a condenser 46 where at least some water vapor is condensed out of the process air, the dried air flows to exhaust 47, and the condensate, which is essentially pure water, flows to the reservoir 21 directly or through a conduit 48. In the area 49 where the condensate enters the reservoir 21, the mixture is dilute. However, it is remixed with concentrated antifreeze 23 within the reservoir before reentering the fuel cells through the coolant inlet manifold 26.
  • FIG. 2 illustrates a portion of the fuel cell power plant 19 including the fuel cell stack 20, which employs evaporative cooling. Air is provided to the air inlet manifold 42 and proceeds through the oxidant flow field channels 41 (FIG. 1) to the air exit manifold 45 and thence into the condenser 46. The air outflow from the condenser 46 is above the water line 51 of the water reservoir 21. The cool dried air is expelled to exhaust 47. The coolant for the condenser 46 may comprise ambient air as illustrated by arrows 52, the volume of which is controlled by a condenser controller 53 that varies the speed of a flow fan 54 in order to adjust the condensation rate as needed. The condenser 46 may serve as a manifold, and the air exit manifold 45 may then be omitted.
  • Fuel provided to a fuel inlet manifold 55 flows to the left, then through a fuel turn manifold 56, after which fuel flows to the right and out through a fuel exit manifold 57; the exhausted fuel may be recycled or consumed in a related process.
  • Coolant from the reservoir 21 flows through a coolant conduit 60 to the coolant inlet manifold 26. The coolant passes into the coolant channels (as described with respect to FIG. 1 hereinbefore) to the top of the fuel cell stack 20, and through the coolant exit manifold 32. Coolant flowing out of the coolant exit manifold 32 is recirculated over the conduit 33 to the reservoir 21. The water in the coolant mixture entering through coolant inlet manifold 26 replaces that which is evaporated into the process air channels 41, as described with respect to FIG. 1 hereinbefore.
  • To ensure that adequate water will be present in the fine pores for evaporation, the pump 22 (FIG. 1) may be disposed at the inlet 37 to draw the coolant into the reservoir 21 from the line 33 as shown in FIG. 3. Or, a pump 60 (FIG. 4) may be used in the line 33 or in any other suitable location to ensure adequate coolant circulation. Usually, a pump will be required in order to assure that the flow of antifreeze mixture is sufficient to provide enough water so that evaporation will occur throughout all portions of all of the fuel cells, and to prevent the antifreeze component from partially or completely filling the pores of the water transport plates.
  • Because the PEG, or other antifreeze, has a viscosity many times higher than that of pure liquid water, the pressure drop across the coolant channels will be high, or, the coolant channels will have to be larger (deeper) to accommodate the coolant flow rates required to cool the stack. Deeper channels decrease the number of cells per unit of stack length compared to fuel cell stacks employing water transport plates and using evaporative cooling. The channel depth will nonetheless be shallower than in systems employing coolant water or similar systems employing an antifreeze mixture to cool the stack using the fluid sensible heat exchange. Thus, the invention will provide power density which is greater than traditional water or antifreeze cooling systems.
  • Detailed descriptions of fuel cells having water transport plates may be found in patent publication US2004/0106034.
  • Referring to FIG. 5, fuel cells 63 which may be used to implement the present invention include anode water transport plates (WTPs) 29 a having fuel reactant gas flow field channels 65 and cathode water transport plates 29 b having oxidant reactant gas (air) flow field channels 66. A membrane electrode assembly (MEA) 70 includes a proton exchange membrane with catalyst on both surfaces. Gas diffusion layers (GDLs) 72 are provided adjacent each surface of the MEAs 70. In the prior art (such as in the aforementioned patent publication US 2004/0106034) the GDLs are typically constructed from carbon fiber sheet material, and are usually wettable. In some known GDLs, there is an additional wet-proof layer deposited on or joined to the GDL to form a bi-layer. The carbon fiber layer may or may not be wet-proofed whether a bi-layer is used or not used.
  • To prevent loss of fuel cell stack performance, the MEAs 70 must be shielded from the non-water component of the antifreeze mixture in the coolant channels 28. Therefore, the invention preferably employs fuel cells 63 with GDLs 72 which are treated, such as with polytetrafluoroethylene (PTFE) to be wet-proofed, or include an additional wet-proof layer.
  • If desired in any utilization of the invention, either the anode WTP 29 a or the cathode WTP 29 b may be solid. A solid WTP will block coolant from reaching the MEA on the side it is located. If the cathode WTP 29 b is solid, water will reach the air (oxidant) flow field channels 66 by migration through the membranes of the MEAs 70 and GDLs 72. Alternatively, the surfaces of one of the WTPs 29, adjacent to the GDL 72, including the reactant gas flow field channels 65, 66, may be wet-proofed by treating with a wet-proofing material, such as PTFE, to shield the membrane from the PEG or other antifreeze on that side.
  • The coolant channels 28 may be formed by having grooves 75 on the opposite surface of the anode water transport plates 29 a from the fuel reactant gas flow field channels 65 which match up with grooves 76 on the opposite surface of cathode water transport plates 29 b from oxidant reactant gas flow field channels 66. Or, the grooves may be in only one plate 29 a, 29 b, the matching surface of the other plate 29 b, 29 a being flat.

Claims (11)

1. A fuel cell power plant (19) comprising:
a stack (20) of fuel cells (63), each fuel cell including water transport plates (29) with coolant channels (28) formed therein or adjacent thereto and with fuel reactant gas flow field channels (65) and oxidant reactant gas flow field channels (66) having inlets and outlets, at least one of said plates being porous and hydrophilic;
a source (42) of oxidant reactant gas in fluid communication with inlets of said oxidant reactant gas flow field channels;
a source (55) of fuel reactant gas in fluid communication with inlets of said fuel reactant gas flow field channels;
a coolant reservoir (21), each of said fuel cell coolant channels being in fluid communication with said coolant reservoir;
a pump (22, 60) for circulating coolant from said reservoir, through said fuel cell coolant channels and back to said reservoir;
characterized by:
said coolant reservoir containing a coolant mixture 23 of water with a miscible, freeze depressing substance; and
a condenser (46), connected to the outlet of at least one of said oxidant reactant gas flow field channels of said fuel cells, condensate of said condenser in fluid communication (48) with said reservoir, said coolant mixture migrating from said coolant channels into said at least one hydrophilic, porous water transport plate of each fuel cell and at least some water within said coolant mixture along with some process water evaporating into at least said reactant gas flow field channels of said at least one porous and hydrophilic plates of each fuel cell to cool said fuel cells, at least some of the water vapor in at least one of said reactant gas flow field channels being condensed in said condenser and returned to said reservoir where it mixes with coolant in said reservoir.
2. A power plant (19) according to claim 1 wherein:
the reactant gas flow field is a fuel channel.
3. A power plant (19) according to claim 1 further characterized by:
each fuel cell (63) including membrane electrode assembly (MEA) (70) having a membrane with catalyst on both surfaces thereof, said MEA configured to provide a wet-proofed barrier between at least one surface of said MEA and said coolant channels.
4. A power plant (19) according to claim 3 wherein said wet-proofed barrier comprises:
at least one wet-proofed gas diffusion layer (72) adjacent said MEA (70) in each of said fuel cells.
5. A power plant (19) according to claim 3 wherein said wet-proofed barrier comprises:
at least one bilayer (70) adjacent said MEA in each of said fuel cells.
6. A power plant (19) according to claim 3 wherein said wet-proofed barrier comprises:
a solid water transport plate (29) on at least one side of said MEA (70).
7. A power plant (19) according to claim 1 further characterized by:
said pump (22) being disposed at an inlet of said reservoir (21) receiving (33) circulating coolant from said coolant channels (28).
8. A power plant (19) according to claim 1 further characterized by:
said pump (60) being disposed in a conduit (33) interconnecting said coolant channels (28) with an inlet (37) of said reservoir (21).
9. A power plant (19) according to claim 1 further comprising:
a condenser controller (53, 54) for controlling the rate of condensation of water vapor in said condenser (46).
10. A power plant (19) according to claim 9 wherein:
said condenser (46) is cooled by a stream of air (52) and said condenser controller is a controller (53) that varies the speed of an air fan (54).
11. A power plant (19) according to claim 9 wherein:
said condenser (46) is cooled by a controlled flow of freeze-proof coolant through flow passages in said condenser.
US12/086,468 2006-05-17 2005-12-01 Evaporative Cooling of Fuel Cells Employing Antifreeze Solution Abandoned US20090053568A1 (en)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
JP2006137862 2006-05-17
JP2006-137862 2006-05-17
JP2006-324195 2006-11-30
JP2006324195 2006-11-30
PCT/JP2007/059862 WO2007132811A1 (en) 2006-05-17 2007-05-14 Rubber composition for tread and tire having tread using the same

Publications (1)

Publication Number Publication Date
US20090053568A1 true US20090053568A1 (en) 2009-02-26

Family

ID=38693902

Family Applications (2)

Application Number Title Priority Date Filing Date
US12/086,468 Abandoned US20090053568A1 (en) 2006-05-17 2005-12-01 Evaporative Cooling of Fuel Cells Employing Antifreeze Solution
US12/224,332 Expired - Fee Related US7741382B2 (en) 2006-05-17 2007-05-14 Rubber composition for tread and tire having tread using same

Family Applications After (1)

Application Number Title Priority Date Filing Date
US12/224,332 Expired - Fee Related US7741382B2 (en) 2006-05-17 2007-05-14 Rubber composition for tread and tire having tread using same

Country Status (6)

Country Link
US (2) US20090053568A1 (en)
EP (1) EP2019126B1 (en)
JP (1) JP4704390B2 (en)
CN (1) CN101443403B (en)
DE (1) DE602007012079D1 (en)
WO (1) WO2007132811A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20180175421A1 (en) * 2016-12-16 2018-06-21 Hyundai Motor Company Fuel cell system

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4805584B2 (en) * 2005-01-21 2011-11-02 住友ゴム工業株式会社 Rubber composition for tread and tire comprising the same
JP5380007B2 (en) 2008-06-16 2014-01-08 富士フイルム株式会社 Anti-counterfeit media
JP5635251B2 (en) * 2009-10-01 2014-12-03 住友ゴム工業株式会社 Rubber composition for tread and pneumatic tire
CN102108144A (en) * 2010-12-24 2011-06-29 中国热带农业科学院农产品加工研究所 Preparation method of epoxidized natural rubber masterbatch with highly dispersed nano-silicon dioxide/carbon black
GB2517318A (en) * 2012-03-22 2015-02-18 Lembaga Getah Malaysia Malaysian Rubber Board An antistatic rubber compound and antistatic tire
MY153723A (en) * 2012-03-22 2015-03-13 Lembaga Getah Malaysia An antistatic rubber compound and antistatic tire
GB201319877D0 (en) * 2013-11-11 2013-12-25 Tun Abdul Razak Res Ct Improvements in the mixing and processing of rubber compositions containing polar fillers
JP6345971B2 (en) * 2014-04-09 2018-06-20 住友ゴム工業株式会社 Pneumatic tire
JP6493077B2 (en) * 2015-08-06 2019-04-03 トヨタ自動車株式会社 Conductor end joining method and end joining structure
JP2025099478A (en) * 2023-12-21 2025-07-03 住友ゴム工業株式会社 Rubber composition and tire

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6316135B1 (en) * 1999-07-22 2001-11-13 International Fuel Cells Llc Direct antifreeze cooled fuel cell
US20030129465A1 (en) * 2000-10-20 2003-07-10 Akinari Nakamura Fuel cell system and method of operating the system
US20040009383A1 (en) * 2002-07-12 2004-01-15 Michels H. Harvey High molecular weight direct antifreeze cooled fuel cell
US20040157094A1 (en) * 2003-02-06 2004-08-12 Reiser Carl A. Fuel cell stack melting of coolant water during frozen startup
US20050048354A1 (en) * 2003-08-27 2005-03-03 Breault Richard D. Fuel cell temperature control by evaporative cooling

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4202023A1 (en) * 1992-01-25 1993-07-29 Degussa HAFTPROMOTER FOR RUBBER AND PLASTIC MIXTURES
US5396940A (en) * 1993-09-17 1995-03-14 The Goodyear Tire & Rubber Company Sulfur cured rubber composition containing epoxidized natural rubber and silica filler
DE4415720C2 (en) * 1994-05-05 1997-09-25 Uniroyal Englebert Gmbh Tire carcass, its manufacture and use
US5929156A (en) * 1997-05-02 1999-07-27 J.M. Huber Corporation Silica product for use in elastomers
US5872176A (en) * 1997-07-11 1999-02-16 Bridgestone Corporation Addition of salts to improve the interaction of silica with rubber
KR100706886B1 (en) * 1998-12-22 2007-04-11 피렐리 타이어 소시에떼 퍼 아찌오니 Tire production method, the tire obtained by the method and the elastomer composition used in the tire
RU2245251C2 (en) * 1998-12-22 2005-01-27 Пирелли Пнеуматичи С.П.А. Method of production of tires and tires manufactured by this method from elastomer compositions
JP4307633B2 (en) 1999-06-04 2009-08-05 住友ゴム工業株式会社 Modified diene rubber composition
FR2804119B1 (en) * 2000-01-24 2002-12-13 Rhodia Chimie Sa PROCESS FOR THE PREPARATION OF MASTER BLENDS BASED ON POLYMER AND MINERAL PARTICLES AND MASTER BLENDS THUS OBTAINED
US7414087B2 (en) * 2003-08-20 2008-08-19 Sumitomo Rubber Industries, Ltd. Rubber composition and pneumatic tire using the same
JP2005089625A (en) * 2003-09-18 2005-04-07 Sumitomo Chemical Co Ltd Rubber composition for anti-vibration rubber and anti-vibration rubber
JP4088259B2 (en) 2004-02-19 2008-05-21 住友ゴム工業株式会社 Rubber composition
JP4583085B2 (en) * 2004-06-25 2010-11-17 住友ゴム工業株式会社 Rubber composition for tread and pneumatic tire using the same
JP4540420B2 (en) * 2004-07-28 2010-09-08 住友ゴム工業株式会社 Rubber composition for tire
JP4805584B2 (en) 2005-01-21 2011-11-02 住友ゴム工業株式会社 Rubber composition for tread and tire comprising the same
JP4860162B2 (en) * 2005-02-14 2012-01-25 住友ゴム工業株式会社 Rubber composition and tire comprising the same

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6316135B1 (en) * 1999-07-22 2001-11-13 International Fuel Cells Llc Direct antifreeze cooled fuel cell
US20030129465A1 (en) * 2000-10-20 2003-07-10 Akinari Nakamura Fuel cell system and method of operating the system
US20040009383A1 (en) * 2002-07-12 2004-01-15 Michels H. Harvey High molecular weight direct antifreeze cooled fuel cell
US6911275B2 (en) * 2002-07-12 2005-06-28 Utc Fuel Cells, Llc High molecular weight direct antifreeze cooled fuel cell
US20040157094A1 (en) * 2003-02-06 2004-08-12 Reiser Carl A. Fuel cell stack melting of coolant water during frozen startup
US20050048354A1 (en) * 2003-08-27 2005-03-03 Breault Richard D. Fuel cell temperature control by evaporative cooling

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20180175421A1 (en) * 2016-12-16 2018-06-21 Hyundai Motor Company Fuel cell system
US10944118B2 (en) * 2016-12-16 2021-03-09 Hyundai Motor Company Fuel cell system for preventing flooding of a fuel cell stack

Also Published As

Publication number Publication date
CN101443403B (en) 2010-11-10
EP2019126B1 (en) 2011-01-19
CN101443403A (en) 2009-05-27
US20090054550A1 (en) 2009-02-26
JP4704390B2 (en) 2011-06-15
EP2019126A1 (en) 2009-01-28
WO2007132811A1 (en) 2007-11-22
DE602007012079D1 (en) 2011-03-03
US7741382B2 (en) 2010-06-22
JP2008156593A (en) 2008-07-10
EP2019126A4 (en) 2009-10-28

Similar Documents

Publication Publication Date Title
US6723461B2 (en) Water management system for fuel cell
US6960404B2 (en) Evaporative cooled fuel cell
KR100986525B1 (en) Evaporative Cooling Fuel Cell System and its Cooling Method
US6322915B1 (en) Humidification system for a fuel cell power plant
US6779351B2 (en) Fuel cell systems with evaporative cooling and methods for humidifying and adjusting the temperature of the reactant streams
JPH06275284A (en) Solid polymer electrolyte film type fuel cell
US20140234740A1 (en) Direct oxidation fuel cell system with uniform vapor delivery of fuel
US20090053568A1 (en) Evaporative Cooling of Fuel Cells Employing Antifreeze Solution
KR101047414B1 (en) Humidifier for fuel cell stack using injector
JPH06325780A (en) Fuel cell system
WO2006071580A2 (en) Fuel cells evaporatively reactant gas cooling and operational freeze prevention
JP2010129482A (en) Fuel cell separator, fuel cell stack, and fuel cell system
US6350535B1 (en) Mist evaporation system for fuel cell hydration
US8507137B2 (en) Separator plate configuration for a fuel cell
US7179557B2 (en) Direct antifreeze cooled fuel cell power plant with passive water management
EP1935046B1 (en) Modified fuel cells with internal humidification and/or temperature control systems
WO2007064338A1 (en) Evaporative cooling of fuel cells employing antifreeze solution
JP2004529458A (en) Method for improving the moisture balance of a fuel cell
US8835063B2 (en) Evaporative humidifier for fuel cell system
US7063907B2 (en) Passive water management system for a fuel cell power plant
CN114144913A (en) Humidifier, fuel cell device with humidifier, and motor vehicle
US7201992B2 (en) Fuel cell with passive water balance
JP2005019221A (en) Fuel cell system
WO2003073529A2 (en) Fuel cell systems with evaporative cooling and methods for humidifying and adjusting the temperature of the reactant streams

Legal Events

Date Code Title Description
AS Assignment

Owner name: UTC FUEL CELLS, LLC, CONNECTICUT

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:MEYERS, JEREMY P.;BALLIET, RAYAN J.;REEL/FRAME:021126/0257;SIGNING DATES FROM 20051122 TO 20051129

Owner name: UTC FUEL CELLS, LLC, CONNECTICUT

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:MEYERS, JEREMY P.;BALLIET, RAYAN J.;SIGNING DATES FROM 20051122 TO 20051129;REEL/FRAME:021126/0257

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION