US20190020051A1 - Electrochemical stack compression system - Google Patents
Electrochemical stack compression system Download PDFInfo
- Publication number
- US20190020051A1 US20190020051A1 US16/133,804 US201816133804A US2019020051A1 US 20190020051 A1 US20190020051 A1 US 20190020051A1 US 201816133804 A US201816133804 A US 201816133804A US 2019020051 A1 US2019020051 A1 US 2019020051A1
- Authority
- US
- United States
- Prior art keywords
- compression
- stack
- compression system
- compression mechanism
- gib
- 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
Links
- 230000006835 compression Effects 0.000 title claims abstract description 123
- 238000007906 compression Methods 0.000 title claims abstract description 123
- 239000000835 fiber Substances 0.000 claims abstract description 31
- 230000007246 mechanism Effects 0.000 claims description 67
- 239000000463 material Substances 0.000 claims description 20
- 238000000034 method Methods 0.000 claims description 8
- 230000008859 change Effects 0.000 claims description 4
- 230000004044 response Effects 0.000 claims description 4
- 229920000049 Carbon (fiber) Polymers 0.000 claims 1
- 239000004917 carbon fiber Substances 0.000 claims 1
- 239000012528 membrane Substances 0.000 description 21
- 239000003792 electrolyte Substances 0.000 description 15
- -1 e.g. Substances 0.000 description 14
- 239000001257 hydrogen Substances 0.000 description 13
- 229910052739 hydrogen Inorganic materials 0.000 description 13
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 12
- 230000008901 benefit Effects 0.000 description 8
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 7
- 238000000576 coating method Methods 0.000 description 7
- 239000001301 oxygen Substances 0.000 description 7
- 229910052760 oxygen Inorganic materials 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 229910001868 water Inorganic materials 0.000 description 7
- 239000011248 coating agent Substances 0.000 description 6
- 239000000446 fuel Substances 0.000 description 6
- 239000007789 gas Substances 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- 229910052782 aluminium Inorganic materials 0.000 description 5
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 5
- 239000010935 stainless steel Substances 0.000 description 5
- 229910001220 stainless steel Inorganic materials 0.000 description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- 239000004677 Nylon Substances 0.000 description 4
- 239000004696 Poly ether ether ketone Substances 0.000 description 4
- 239000004698 Polyethylene Substances 0.000 description 4
- 229910000831 Steel Inorganic materials 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 230000005611 electricity Effects 0.000 description 4
- 238000005516 engineering process Methods 0.000 description 4
- 150000002739 metals Chemical class 0.000 description 4
- 229920001778 nylon Polymers 0.000 description 4
- 229920002530 polyetherether ketone Polymers 0.000 description 4
- 229920000573 polyethylene Polymers 0.000 description 4
- 239000010959 steel Substances 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000004642 Polyimide Substances 0.000 description 3
- 229920006362 Teflon® Polymers 0.000 description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 3
- 229910045601 alloy Inorganic materials 0.000 description 3
- 239000000956 alloy Substances 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 239000000919 ceramic Substances 0.000 description 3
- 230000003247 decreasing effect Effects 0.000 description 3
- 238000003780 insertion Methods 0.000 description 3
- 230000037431 insertion Effects 0.000 description 3
- 229910001092 metal group alloy Inorganic materials 0.000 description 3
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 229920001721 polyimide Polymers 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 3
- 239000004810 polytetrafluoroethylene Substances 0.000 description 3
- 230000009467 reduction Effects 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- 229910052719 titanium Inorganic materials 0.000 description 3
- 239000010936 titanium Substances 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000004020 conductor Substances 0.000 description 2
- 238000013461 design Methods 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- 238000005868 electrolysis reaction Methods 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- 239000007800 oxidant agent Substances 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 229910001018 Cast iron Inorganic materials 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 101100437784 Drosophila melanogaster bocks gene Proteins 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 229920000271 Kevlar® Polymers 0.000 description 1
- 229920000914 Metallic fiber Polymers 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- NRTOMJZYCJJWKI-UHFFFAOYSA-N Titanium nitride Chemical compound [Ti]#N NRTOMJZYCJJWKI-UHFFFAOYSA-N 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 239000004760 aramid Substances 0.000 description 1
- 229920003235 aromatic polyamide Polymers 0.000 description 1
- 229910010293 ceramic material Inorganic materials 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 239000012809 cooling fluid Substances 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 239000002001 electrolyte material Substances 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 239000002803 fossil fuel Substances 0.000 description 1
- 239000003502 gasoline Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 229910001026 inconel Inorganic materials 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 229910001463 metal phosphate Inorganic materials 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920005597 polymer membrane Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 230000036316 preload Effects 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 238000013519 translation Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- LEHFSLREWWMLPU-UHFFFAOYSA-B zirconium(4+);tetraphosphate Chemical class [Zr+4].[Zr+4].[Zr+4].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LEHFSLREWWMLPU-UHFFFAOYSA-B 0.000 description 1
Images
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M8/00—Fuel cells; Manufacture thereof
- H01M8/24—Grouping of fuel cells, e.g. stacking of fuel cells
- H01M8/2465—Details of groupings of fuel cells
- H01M8/247—Arrangements for tightening a stack, for accommodation of a stack in a tank or for assembling different tanks
- H01M8/2475—Enclosures, casings or containers of fuel cell stacks
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
- C25B1/00—Electrolytic production of inorganic compounds or non-metals
- C25B1/01—Products
- C25B1/02—Hydrogen or oxygen
- C25B1/04—Hydrogen or oxygen by electrolysis of water
-
- C25B1/12—
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
- C25B9/00—Cells or assemblies of cells; Constructional parts of cells; Assemblies of constructional parts, e.g. electrode-diaphragm assemblies; Process-related cell features
- C25B9/05—Pressure cells
-
- C25B9/206—
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
- C25B9/00—Cells or assemblies of cells; Constructional parts of cells; Assemblies of constructional parts, e.g. electrode-diaphragm assemblies; Process-related cell features
- C25B9/70—Assemblies comprising two or more cells
- C25B9/73—Assemblies comprising two or more cells of the filter-press type
- C25B9/77—Assemblies comprising two or more cells of the filter-press type having diaphragms
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M8/00—Fuel cells; Manufacture thereof
- H01M8/24—Grouping of fuel cells, e.g. stacking of fuel cells
- H01M8/2465—Details of groupings of fuel cells
- H01M8/247—Arrangements for tightening a stack, for accommodation of a stack in a tank or for assembling different tanks
- H01M8/248—Means for compression of the fuel cell stacks
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/30—Hydrogen technology
- Y02E60/36—Hydrogen production from non-carbon containing sources, e.g. by water electrolysis
-
- Y02E60/366—
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/30—Hydrogen technology
- Y02E60/50—Fuel cells
Definitions
- Embodiments of the present disclosure relate to electrochemical cells, and more particularly, to systems for applying a compressive force to high differential pressure electrochemical cell stacks.
- Electrochemical cells are used to generate an electric current from chemical reactions. Electrochemical cell technology, like fuel cells and hydrogen compressors, offers a promising alternative to traditional power sources, such as fossil fuels, for a range of technologies, including, for example, transportation vehicles, portable power supplies, and stationary power production.
- An electrochemical cell converts the chemical energy of a proton source (e.g., hydrogen, natural gas, methanol, gasoline, etc.) into electricity through a chemical reaction with oxygen or another oxidizing agent. The chemical reaction typically yields electricity, heat, and water.
- a proton source e.g., hydrogen, natural gas, methanol, gasoline, etc.
- a basic high differential pressure electrochemical cell comprises a negatively charged anode, a positively charged cathode, and an ion-conducting material called an electrolyte.
- Different electrochemical cell technologies utilize different electrolyte materials.
- a Proton Exchange Membrane (PEM) cell for example, utilizes a polymeric, ion-conducting membrane as the electrolyte.
- a fuel such as hydrogen gas
- hydrogen may be split into positively charged protons and negatively charged electrons.
- the protons may then pass through an electrolyte membrane, such as a PEM, to a cathode side of the cell.
- the PEM may be configured to allow only the positively charged protons to pass through to the cathode side of the cell.
- the negatively charged electrons may be forced to pass through an external electric load circuit to reach the cathode side of the cell, and in doing so, may generate a usable electrical current.
- Oxygen may be delivered to the cathode side of the cell, where it may react with the protons and the electrons to form water molecules and heat as waste.
- the cathode, electrolyte membrane, and anode of an individual electrochemical cell may collectively form a “membrane electrode assembly” (MEA), which may be supported on both sides by bipolar plates.
- Gases, such as hydrogen and oxygen, may be supplied to the electrodes of the MEA through channels or grooves formed in the bipolar plates.
- a single cell may generally produce a relatively small electrical potential, about 0.2-1 volt, depending on the current.
- individual electrochemical cells may be stacked together, typically in series, to form an electrochemical cell stack. The number of individual cells in a stack may depend on the application and the amount of output required from the stack for that application.
- the electrochemical cell stack may receive flows of hydrogen and oxygen, which may be distributed to the individual cells. Proper operation of the cell stack may require the maintenance of effective seals between the individual cells, components of the cells, and flow conduits. Accordingly, the electrochemical cells in a stack may need to be compressed against one another to maintain sufficient electrical contact between the internal components of each cell. The amount of compression between the cells may affect the contact resistance, electrical conduction, and membrane porosity, and thus may affect the overall performance of the electrochemical cells. Accordingly, in order to maintain contact between the cells and increase performance, uniform compression is typically distributed over the electrochemical cell stack.
- tie rods, bands, and/or springs may be used to apply compressive force to a cell stack.
- These compression mechanisms typically require the use of end plates located at both ends of the electrochemical cell stack.
- end plates may cap each end of a cell stack, and tie rods may extend from one end plate to the other, either external to the stack along the periphery, or within the stack by passing through openings in the cells of the stack.
- the tie rods may be tightened or loosened to move the end plates towards or away from each other to adjust the amount of compression exerted on the stack.
- bands may also be wrapped around the stack, stretching from end plate to end plate, to maintain compression.
- the present disclosure is directed toward the design of improved compression systems for use with electrochemical cells.
- the present disclosure is directed towards the design of adjustable compression structures for use with electrochemical cells.
- Such devices may be used in electrochemical cells operating under high differential pressures, including, but not limited to hydrogen compressors, fuel cells, electrolysis cells, hydrogen purifiers, and hydrogen expanders.
- Embodiments of the present disclosure are directed to a system for applying compressive force to electrochemical cell stacks.
- an electrochemical cell stack compression system may include an integral, hollow frame configured to contain a plurality of electrochemical cells arranged along an axis in a stack configuration, wherein the frame has a defined shape and forms a continuous border around a periphery of the electrochemical cell stack when inserted, and wherein the frame is formed of a plurality of fibers.
- the frame may be formed of a plurality of fibers composed of different materials; the frame may include multiple layers formed of fibers; the frame may include a friction-reducing layer located between at least one of the multiple layers formed of fibers; the frame may include at least two opposing wall surfaces; the frame may be further configured to contain at least one end block located at an end region of the frame; the frame may be further configured to contain at least one compression mechanism configured to apply a compressive force to the electrochemical cell stack; the compression mechanism may include at least one gib; the compression mechanism may be configured to expand when heated; the compression mechanism may include one or more internal drive screws extending between two separate portions, wherein rotating the internal drive screws in one direction moves the two portions further away from each other and rotating the internal drive screws in the opposite direction moves the two portions closer to each other; and the frame may be configured to accommodate multiple different sizes of electrochemical cell stacks.
- an electrochemical stack compression system may include a structure having a defined shape that is configured to receive and contain a plurality of electrochemical cells arranged in a series along an axis to form an electrochemical stack and at least one compression mechanism configured to apply a compressive force to the electrochemical stack located adjacent to and along the axis of the electrochemical stack, wherein the structure forms a continuous border surrounding the electrochemical stack and the at least one compression mechanism when contained.
- the compression mechanism may include at least one gib; the compression mechanism may include a block that is configured to expand in response to an increase in temperature; the compression mechanism may include internal drive screws configured to increase the size of the compression mechanism when the internal drive screws are rotated in a first direction and to decrease the size of the compression mechanism when the internal drive screws are rotated in a second direction opposite the first direction; the structure may be formed of wound fibers; the fibers may be non-conductive; the fibers may be carbon; and a height of the structure along the axis of the electrochemical stack may change in response to a load applied by the compression mechanism to the electrochemical stack when receiving the compression mechanism.
- a method of preloading various embodiments of the disclosure may include inserting the electrochemical stack into the structure, inserting the at least one compression mechanism into the structure, configuring the compression mechanism to apply a predetermined load within the compression system, and measuring a change in height of the structure along the axis of the electrochemical stack to determine the load being applied by the compression mechanism.
- Various embodiments of the method may further include: inserting at least one end block into the structure; the compression mechanism may include two gibs and configuring the compression mechanism may include wedging the two gibs against each other; configuring the compression mechanism may include increasing the temperature of the compression system to expand the compression mechanism; and configuring the compression mechanism includes rotating a plurality of internal drive screws to expand the compression mechanism.
- an electrochemical stack compression system may include an integral, hollow structure having a defined shape and formed of a plurality of wound fibers; a plurality of electrochemical cells arranged in a series along an axis to form an electrochemical stack, wherein the electrochemical stack is contained within the structure; at least one end block contained within the structure and located at an end region of the structure; and at least one compression mechanism contained within the structure, wherein the at least one compression mechanism is configured to apply a compressive force to the electrochemical stack, and wherein the electrochemical stack, the at least one end block, and the at least one compression mechanism are contained in series within the structure such that the structure forms a continuous border around and adjacent to a periphery of the electrochemical stack, the at least one end block, and the at least one compression mechanism.
- the fibers may be configured to stretch and contract in response to changes in the compressive force;
- the at least one compression mechanism may include a gib; and the at least one compression mechanism may be configured to expand.
- FIG. 1 illustrates an exploded view of an exemplary electrochemical cell, according to an embodiment of the present disclosure.
- FIG. 2A illustrates an exemplary electrochemical cell compression system, according to an embodiment of the present disclosure.
- FIG. 2B illustrates an exemplary electrochemical cell compression system, according to an embodiment of the present disclosure.
- FIG. 2C illustrates a cross-section of the exemplary electrochemical cell compression system of FIG. 2A .
- FIG. 3A illustrates an exemplary compression mechanism for an electrochemical cell compression system according to an exemplary embodiment of the present disclosure.
- FIG. 3B illustrates an alternative view of the exemplary compression mechanism of FIG. 3A .
- FIG. 4 illustrates an exemplary compression mechanism for an electrochemical cell compression system according to an exemplary embodiment of the present disclosure.
- FIG. 1 depicts an individual electrochemical cell 10 , according to an embodiment of the present disclosure.
- cell 10 includes a central, electrolyte membrane 8 .
- Electrolyte membrane 8 may be positioned between an anode 7 A and a cathode 7 B. Together, electrolyte membrane 8 , anode 7 A, and cathode 7 B may form MEA 3 .
- Hydrogen atoms supplied to anode 7 A may be electrochemically split into electrons and protons. The electrons may flow through an electric circuit (not shown) to cathode 7 B, generating electricity in the process, while the protons may pass through electrolyte membrane 8 to cathode 7 B.
- protons may react with electrons and oxygen supplied to cathode 7 B to produce water and heat.
- Electrolyte membrane 8 may electrically insulate anode 7 A from cathode 7 B.
- Electrolyte membrane 8 may be any suitable membrane, including, e.g., a PEM membrane.
- Electrolyte membrane 8 may be formed of a pure polymer membrane or a composite membrane, which may include, e.g., silica, heteropolyacids, layered metal phosphates, phosphates, and zirconium phosphates, embedded in a polymer matrix. Electrolyte membrane 8 may be permeable to protons but may not conduct electrons.
- Anode 7 A and cathode 7 B may include porous carbon electrodes containing a catalyst.
- the catalyst material e.g., platinum or any other suitable material, may speed up the reaction of oxygen and fuel.
- the size and shape of MEA 3 may be increased or decreased depending on the application of cell 10 and the given load requirements.
- the thickness, length, or width of MEA 3 may be adjusted according to the given application and requirements.
- the concentration of catalyst material in anode 7 A and cathode 7 B may be adjusted according to the given application.
- the concentration of catalyst material in anode 7 A and cathode 7 B and the thickness of electrolyte membrane 8 may each affect the total thickness of MEA 3 .
- electrochemical cell 10 may optionally include one or more electrically conductive flow structures 5 on each side of MEA 3 .
- Flow structures 5 may serve as diffusion media enabling the transport of gases and liquids within cell 10 .
- Flow structures 5 may also promote electrical conduction, aid in the removal of heat and water from electrochemical cell 10 , and provide mechanical support to electrolyte membrane 8 .
- Flow structures 5 may include, e.g., flow fields, gas diffusion layers (GDL), or any suitable combination thereof.
- Flow structures 5 may be formed of “frit”-type sintered metals, layered structures, e.g., screen packs and expanded metals, and three-dimensional porous substrates.
- An exemplary porous metallic substrate may consist of two distinct layers having different average pore sizes.
- Such flow structures 5 may be formed of any suitable material, including, e.g., metals or metal alloys, such as, e.g., stainless steel, titanium, aluminum, nickel, iron, and nickel-chrome alloys, or any combination thereof.
- flow structures 5 may include a suitable coating, such as a corrosion-resistant coating, like carbon, gold, or titanium-nitride.
- the reactant gases on each side of the electrolyte membrane are often present at different pressures, e.g., operating pressures may range from approximately 0 psid to 15,000 psid, creating a pressure differential across MEA 3 .
- operating pressures may range from approximately 0 psid to 15,000 psid, creating a pressure differential across MEA 3 .
- the pressure differential may create a force on MEA 3 that causes MEA 3 to move away from the high pressure side toward the low pressure side. This movement may cause a reduction in contact pressure and separation of the contacting surface of MEA 3 from flow structures 5 on the high-pressure side.
- Reduction in pressure and subsequent separation between the contacting surfaces of MEA 3 and high-pressure flow structures 5 may reduce the electrical conduction and increase the contact resistance between the two, reducing the efficiency of electrochemical cell 10 .
- cell 10 may also include two bipolar plates 2 A, 2 B.
- Bipolar plate 2 A may be positioned on the high-pressure side
- bipolar plate 2 B may be positioned on the low-pressure side of electrochemical cell 10 .
- Bipolar plates 2 A, 2 B may separate cell 10 from neighboring electrochemical cells (not shown) in a stack. In some embodiments, two adjacent cells in an electrochemical cell stack may share a common bipolar plate.
- Bipolar plates 2 A, 2 B may act as current collectors, may provide access channels for the fuel and the oxidant to reach the respective electrode surfaces, and may provide channels for the removal of water formed during operation of electrochemical cell 10 by means of exhaust gas. Bipolar plates 2 A, 2 B may also provide access channels for cooling fluid, such as, e.g., water, glycol, or a combination thereof. Bipolar plates 2 A, 2 B may be made from aluminum, steel, stainless steel, titanium, copper, nickel-chrome alloy, graphite, or any other suitable electrically conductive material or combination of materials.
- FIGS. 2A through 2C show exemplary electrochemical cell stack compression systems 20 , according to embodiments of the present disclosure.
- Each individual cell 10 may be stacked within compression system 20 to form an electrochemical cell stack 11 .
- Stack 11 may be comprised of any suitable number of cells 10 .
- Stack 11 may be located between end blocks 12 A and 12 B, which may be located at each end of stack 11 .
- End blocks 12 A, 12 B may be formed of any suitable metal, plastic, or ceramic material having adequate compressive strength, e.g., aluminum, steel, stainless steel, cast iron, titanium, polyvinyl chloride, polyethylene, polypropylene, nylon, polyether ether ketone, alumina, or any combination thereof.
- Stack 11 and end blocks 12 A, 12 B may be housed in a structure 15 .
- a wound fiber structure 15 may provide a resilient frame capable of housing a high-pressure electrochemical cell stack without significantly increasing the weight or size of the electrochemical cell system.
- Structure 15 may form a frame with a defined shape into which stack 11 and end blocks 12 A, 12 B are positioned.
- FIG. 2A depicts an elongated, rounded, structure 15 , but structure 15 may be any suitable shape, including, e.g., rectangular, oval, circular, or square.
- the walls of structure 15 may form a continuous border long the periphery of stack 11 and end blocks 12 A, 12 B, and structure 15 and may or may not enclose the front and/or back portions of stack 11 and end blocks 12 A, 12 B.
- End bocks 12 A, 12 B, stack 11 , and any other components housed in structure 15 may be configured to lie flush with the walls of structure 15 on an open face, or the components may be recessed within structure 15 or they may protrude from structure 15 , or any suitable combination thereof.
- Structure 15 may be dimensioned to house end blocks 12 A, 12 B and stack 11 , which may include any suitable number of electrochemical cells 10 .
- the size, e.g., the height H, length L (shown in FIG. 2C ), and/or width, of structure 15 may vary, for example, structure 15 may be configured to stretch during pre-loading, as discussed further below.
- Structure 15 may be dimensioned so as to snugly fit the desired contents, for example, electrochemical stack 11 and end blocks 12 A, 12 B, so as to not substantially increase the size of the overall electrochemical cell system.
- structure 15 may be formed of wound fibers that are capable of stretching and contracting.
- structure 15 may be formed of wound fibers, such as, e.g., carbon, glass, or aramid (e.g., KEVLAR®) fibers.
- the fibers may be non-conductive to reduce the likelihood of short-circuiting stack 11 .
- structure 15 may be formed of metallic fibers, such as, e.g., steel, stainless steel, or aluminum, or alloys, such as Inconel.
- Structure 15 may be formed of homogenous fibers or a mixture of different fibers. Additionally, structure 15 may be formed with or without an epoxy matrix or other suitable material to bind the fibers together. As is shown in FIG.
- the walls of structure 15 may have a thickness ct.
- the wound fiber material properties, such as, e.g., tensile strength, and wall thickness t may be selected to achieve a desired compressive force on stack 11 .
- the fibers making up structure 15 may be wound together to form one integral frame unit into which stack 11 and various other components fit.
- structure 15 may be formed of multiple layers 13 A, 13 B, and 13 C. Though FIG. 2B depicts 3 layers, multi-layered embodiments of structure 15 may include any suitable number of layers. Each layer may be formed of homogenous fibers or of a combination of different fibers. The layers may be attached to one another, via, e.g., bonding or fastening mechanisms, or may be unattached and held together through, e.g., friction. Additionally, some layers may be attached while other layers may be unattached. In the multi-layer embodiments, structure 15 may include one or more slip-planes 4 between the layers.
- Slip-plane 4 may be formed of a separate layer or of a coating on one of the layers, such as, e.g., a polytetrafluoroethylene (e.g., TEFLON®), polyetheretherketone, polyimide, nylon, polyethylene, or polymer layer or coating, or any other suitable friction-reducing material to decrease the friction between the layers. If incorporated, slip-plane 4 may be included between each layer or may be included between fewer than all of the layers. The inclusion of slip-plane 4 may reduce the amount of stress within structure 15 and compression system 20 , particularly in embodiments having thicker structure walls.
- a polytetrafluoroethylene e.g., TEFLON®
- polyetheretherketone polyimide
- nylon polyethylene
- polymer layer or coating any other suitable friction-reducing material to decrease the friction between the layers.
- slip-plane 4 may be included between each layer or may be included between fewer than all of the layers. The inclusion of slip-plane 4 may reduce the amount of stress
- end blocks 12 A, 12 B may be also be configured to fit into structure 15 so that one or both of end blocks 12 A, 12 B may move within structure 15 .
- end blocks 12 A, 12 B may be allowed to slip along the walls of structure 15 . This configuration may decrease the stress in structure 15 , which may in turn allow for structure 15 to incorporate thinner walls.
- end blocks 12 A, 12 B may include a suitable friction reducing material or coating, e.g., polytetrafluoroethylene (e.g., TEFLON®), polyetheretherketone, polyimide, nylon, polyethylene.
- end blocks 12 A, 12 B may be attached to the walls of structure 15 or may be otherwise configured so that end blocks 12 A, 12 B may not slip once inserted into structure 15 .
- compression system 20 may include one or more gibs to promote uniform compression of electrochemical stack 11 within structure 15 .
- the gibs may act as a wedge to drive two parallel planes in structure 15 apart as the gibs are wedged together in a direction perpendicular to the two parallel planes.
- gibs 14 A, 14 B may be inserted between electrochemical cell stack 11 and end block 12 A to drive stack 11 and end block 12 A apart while maintaining their parallel orientation.
- Gib 14 B may have a flat surface and an opposite, angled surface. Gib 14 B may be inserted into structure 15 so that the flat surface lies adjacent to stack 11 and the angled surface faces upwards.
- Gib 14 B may be oriented so that the upward-facing, angled surface slopes in a downward direction toward the front face of structure 15 being loaded. Gib 14 A may then be inserted next to gib 14 B, and the two gibs may be driven together. Gib 14 A may also have a flat surface and an opposite, angled surface sloped at an angle complimentary to the sloped surface of gib 14 B. The angled surface of gib 14 A may be inserted adjacent the angled surface of gib 14 B so that the angled surface also slopes in downward direction towards the front face of structure 15 . Thus, as gib 14 A is inserted into structure 15 and driven against 14 B, the complimentary slopes may slide against each other, pushing the flat surfaces of gibs 14 A, 14 B further apart from each other and towards end block 12 A and stack 11 . Gib 14 A may be inserted into structure 15 until a desired compressive force is exerted on stack 11 .
- Gib 14 B may also include a grip portion configured to aid in the insertion and removal of gibs 14 A, 14 B from structure 15 .
- gib 14 B may include one or more gripping mechanism configured to engage the walls of structure 15 to reduce movement of gib 14 B as gib 14 A is inserted.
- the gripping mechanisms of gib 14 B may engage an inner surface of structure 15 or may extend from gib 14 B and engage an edge and/or outer surface of structure 15 .
- FIG. 2A depicts hooks 9 protruding outwards from gib 14 B and engaging the edges of opposite walls of structure 15 . Hooks 9 may prevent gib 14 B from sliding further into structure 15 as gib 14 A is inserted.
- Gib 14 B may include any suitable gripping mechanism or combination of gripping mechanisms, such as, e.g., protrusions like pegs or hooks, or textured surfaces to reduce movement as gib 14 A is wedged against gib 14 B.
- the gripping mechanisms may be any suitable size, shape, and orientation.
- the thick end of gib 14 B may be constrained against a fixed surface as gib 14 A is driven, preventing translation against cell stack 11 .
- gibs 14 A, 14 B may be included in any suitable position, for example, gibs 14 A, 14 B may be positioned between stack 11 and end block 12 B, or sets of gibs may be located on either side of stack 11 .
- Gibs 14 A, 14 B may be formed of any suitable material, such as, e.g., steel, stainless steel, ceramic, or aluminum. Gibs 14 A, 14 B may also have any suitable coating, such as a lubricant, to reduce galling or to facilitate insertion into compression system 20 .
- a suitable friction reducing material may include, e.g., polytetrafluoroethylene (e.g., TEFLON®), polyetheretherketone, polyimide, nylon, polyethylene, or other lubricious polymer coatings, or any other suitable material.
- Gibs 14 A, 14 B may be any suitable shape and size for insertion into structure 15 .
- the size and shape of gibs 14 A, 14 B may at least in part reflect the size and shape of the interior region of structure 15 .
- Gibs 14 A, 14 B may be designed with any suitable angle.
- the angle that gibs 14 A, 14 B are designed with may be based, at least in part, on the required pre-load of stack 11 , which may be based on the application of stack 11 and the accompanying output requirements.
- the size and shape of gibs 14 A, 14 B may also be based, in part, on the size of stack 11 compared to the size of structure 15 .
- the same size structure 15 may be used to house stacks 11 of different sizes.
- larger gibs 14 A, 14 B may be used with smaller stacks 11 to apply an appropriate compressive force, and vice versa.
- Gibs 14 A, 14 B may be used to apply compression to stack 11 , maintain a uniform load, stabilize system 20 , and provide planarity.
- components of compression system 20 such as stack 11 and end blocks 12 A, 12 B may be inserted into structure 15 .
- structure 15 may be “pre-loaded” or pre-stretched to apply a predetermined compressive force to stack 11 in order to maintain contact between electrochemical cells 10 . This may be accomplished using compressive mechanisms, such as gibs 14 A, 14 B. Once the other components are inserted, gibs 14 A, 14 B may be inserted into structure 15 to fill any gaps.
- Gibs 14 A, 14 B may be wedged against each other until their parallel surfaces are forced apart far enough to achieve a desired compressive load on the surrounding components, e.g., stack 11 , within structure 15 .
- tension within the walls of wound fiber structure 15 may increase, and the fibers may stretch. This may increase the height H of structure 15 .
- the amount of expansion of structure 15 may depend, at least in part, on the wall thickness t and the types of fibers that make up structure 15 . Measuring the change in height H of structure 15 during pre-loading may indicate the compressive force being applied to stack 11 and may allow for more precise control of pre-loading conditions.
- system 20 may provide a lightweight, low-cost system for accurately and effectively applying a compressive load to stack 11 .
- structure 15 may begin to stretch more than its pre-loaded value.
- structure 15 may be forced to stretch more than the pre-loaded value due to differential thermal expansion and the force applied to the stack will increase.
- the materials of structure 15 and any compressive mechanisms may be selected based on their thermal properties to reduce the potential for loss of compressive force during operation.
- system 20 may include other compressive mechanisms instead of, or in addition to, gibs 14 A, 14 B.
- one or more thermal expansion blocks 21 may be used to apply compression to stack 11 .
- Block 21 may be cooled to a temperature below that of stack 11 .
- cooled block 21 may be inserted into compression system 20 .
- Block 21 may expand, and accordingly, may apply compression to stack 11 .
- Block 21 may be formed of any material or combination of materials having suitable thermal expansion characteristics, such as, e.g., suitable metals, metal alloys, or ceramics.
- block 21 may be formed of materials with a higher coefficient of thermal expansion than that of structure 15 .
- operating temperature generally between 30 and 100° C.
- block 21 may expand more than structure 15 . Such expansion may result in compressive loading of stack 11 .
- block 21 may be easier to insert into structure 15 . Inserting block 21 prior to thermal expansion may reduce the wear and stress on the surrounding components of compression system 20 .
- a gap 17 may exist in compression system 20 .
- gap 17 may disappear as block 21 expands and fills the surrounding space (shown in FIG. 3B ).
- the continued expansion of block 21 may begin to compress stack 11 and apply a compressive load.
- the thermal properties of block 21 may be chosen to impart a desired compressive load based on the size of stack 11 and the size of gap 17 in structure 15 . It will be understood that while gap 17 is shown between inserted block 21 and end block 12 A, block 21 may be oriented so that gap 17 occurs on either side of block 21 , or on both sides of block 21 . Further, gap 17 may occur in any region within structure 15 .
- block 21 is herein described as the expansion member, one or more of end blocks 12 A or 12 B may be designed to provide thermal compression instead of, or in addition to, block 21 .
- gibs 14 A, 14 B may also be made of suitable material to allow them to apply compression via use as a wedge as well as through thermal expansion. Additionally, multiple thermal expansion blocks 21 may be used, or a combination of thermal expansion block 21 and gibs 14 A, 14 B may be inserted into structure 15 .
- a screw compression unit 19 with internal drive screws may be used to apply a compressive load.
- Compression unit 19 may be configured to be removable from structure 15 or may be attached to structure 15 .
- threaded screws 18 may extend from a base 16 B of compression unit 19 .
- the opposite ends of screws 18 may extend into complimentary threaded inlets (not shown) in block 16 A of compression unit 19 .
- Rotating screws 18 in one direction may cause screws 18 to screw further into the threaded inlets in block 16 A, moving block 16 A closer to base 16 B and decreasing the gap between 16 A and 16 B. Decreasing the gap between 16 A and 16 B may reduce the compressive force applied to stack 11 .
- Rotating screws 18 in the opposite direction may cause screws 18 to unscrew from the threaded inlets in block 16 A, moving block 16 A away from base 16 B and increasing the gap between 16 A and 16 B. Increasing the gap between 16 A and 16 B may increase the compressive force applied to stack 11 .
- compression unit 19 may be inserted into structure 15 while there is little or no gap between block 16 A and base 16 B. Once inserted, screws 18 may be rotated so as to increase the gap between block 16 A and base 16 B in order to apply a desired compressive force to stack 11 .
- any suitable number of threaded components may be included in compression unit 19 . Additionally, the threaded components may be distributed on base 16 B in any suitable arrangement. Screws 18 may be any suitable shape or size and may be formed of any suitable material, for example, any metal, metal alloy, or ceramic. Any number of compression units 19 may be incorporated in system 20 , and compression unit 19 may be used in place of or in addition to either or both of gibs 14 A, 14 B and thermal expansion block 21 . Further, in some embodiments, compression unit 19 may also be incorporated into one of the components or compression mechanisms described previously. For example, one or more of end blocks 12 A, 12 B, gibs 14 A, 14 B, or block 21 may include internal drive screws.
- compression system 20 may accommodate electrochemical stacks of different sizes.
- structure 15 may be configured to receive electrochemical cell stacks of different sizes with different numbers of electrochemical cells suitable for different applications and output levels. If a smaller stack 11 with fewer electrochemical cells 10 is contained in structure 15 , then larger compression mechanisms or a larger number of or combination of compression mechanisms may be inserted around stack 11 during pre-loading to fill any additional space and apply a desired compressive force.
- the same basic structure 15 may be capable of housing different sized electrochemical cell stacks appropriate for different applications and different output levels. This may reduce manufacturing costs, because one standard structure 15 may be produced for housing a variety of electrochemical cell stack sizes suitable for a variety of applications. Thus, the same basic technology may produce structures for stacks of various cell counts and sizes. By incorporating different numbers of or different types of compression mechanisms described above, the same structure 15 may be capable of accommodating a range of operating conditions over an extended period of time.
- structure 15 may be configured so that one or more of the layers is removable or separable from the other layers.
- one or more of the layers may be nested within another layer and may be capable of being completely removed from the surrounding layer.
- layer 13 A may be nested within and removable from layer 13 B, for example, and slip-plane 4 may facilitate removal.
- one or more layers may be removed to adapt structure 15 to the currently applicable operating conditions.
- Application of embodiments described above may improve performance of electrochemical cells, including electrochemical cells operating under high-pressure conditions.
Landscapes
- Chemical & Material Sciences (AREA)
- Electrochemistry (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Metallurgy (AREA)
- Materials Engineering (AREA)
- General Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Sustainable Energy (AREA)
- Sustainable Development (AREA)
- Manufacturing & Machinery (AREA)
- Inorganic Chemistry (AREA)
- Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)
- Fuel Cell (AREA)
- Secondary Cells (AREA)
Abstract
Description
- This patent application is a divisional of U.S. application Ser. No. 14/198,317, filed Mar. 5, 2014, which claims the benefit of priority under 35 U.S.C. § 120 to U.S. Provisional Patent Application No. 61/775,068, filed Mar. 8, 2013, which are incorporated herein by reference in their entirety.
- Embodiments of the present disclosure relate to electrochemical cells, and more particularly, to systems for applying a compressive force to high differential pressure electrochemical cell stacks.
- Electrochemical cells are used to generate an electric current from chemical reactions. Electrochemical cell technology, like fuel cells and hydrogen compressors, offers a promising alternative to traditional power sources, such as fossil fuels, for a range of technologies, including, for example, transportation vehicles, portable power supplies, and stationary power production. An electrochemical cell converts the chemical energy of a proton source (e.g., hydrogen, natural gas, methanol, gasoline, etc.) into electricity through a chemical reaction with oxygen or another oxidizing agent. The chemical reaction typically yields electricity, heat, and water.
- A basic high differential pressure electrochemical cell comprises a negatively charged anode, a positively charged cathode, and an ion-conducting material called an electrolyte. Different electrochemical cell technologies utilize different electrolyte materials. A Proton Exchange Membrane (PEM) cell, for example, utilizes a polymeric, ion-conducting membrane as the electrolyte.
- To generate electricity, a fuel, such as hydrogen gas, for example, may be delivered to an anode side of an electrochemical cell. Here, hydrogen may be split into positively charged protons and negatively charged electrons. The protons may then pass through an electrolyte membrane, such as a PEM, to a cathode side of the cell. The PEM may be configured to allow only the positively charged protons to pass through to the cathode side of the cell. The negatively charged electrons may be forced to pass through an external electric load circuit to reach the cathode side of the cell, and in doing so, may generate a usable electrical current. Oxygen may be delivered to the cathode side of the cell, where it may react with the protons and the electrons to form water molecules and heat as waste.
- The cathode, electrolyte membrane, and anode of an individual electrochemical cell, may collectively form a “membrane electrode assembly” (MEA), which may be supported on both sides by bipolar plates. Gases, such as hydrogen and oxygen, may be supplied to the electrodes of the MEA through channels or grooves formed in the bipolar plates.
- A single cell may generally produce a relatively small electrical potential, about 0.2-1 volt, depending on the current. To increase the total voltage output, individual electrochemical cells may be stacked together, typically in series, to form an electrochemical cell stack. The number of individual cells in a stack may depend on the application and the amount of output required from the stack for that application.
- The electrochemical cell stack may receive flows of hydrogen and oxygen, which may be distributed to the individual cells. Proper operation of the cell stack may require the maintenance of effective seals between the individual cells, components of the cells, and flow conduits. Accordingly, the electrochemical cells in a stack may need to be compressed against one another to maintain sufficient electrical contact between the internal components of each cell. The amount of compression between the cells may affect the contact resistance, electrical conduction, and membrane porosity, and thus may affect the overall performance of the electrochemical cells. Accordingly, in order to maintain contact between the cells and increase performance, uniform compression is typically distributed over the electrochemical cell stack.
- Often tie rods, bands, and/or springs may be used to apply compressive force to a cell stack. These compression mechanisms typically require the use of end plates located at both ends of the electrochemical cell stack. For example, end plates may cap each end of a cell stack, and tie rods may extend from one end plate to the other, either external to the stack along the periphery, or within the stack by passing through openings in the cells of the stack. The tie rods may be tightened or loosened to move the end plates towards or away from each other to adjust the amount of compression exerted on the stack. In some instances, bands may also be wrapped around the stack, stretching from end plate to end plate, to maintain compression. To withstand the compressive forces of tie rods and/or bands, thicker end plates and rods may be required to prevent bowing or cracking. This may increase the size and weight of the cell stack, as well as the cost of the electrochemical cell system. The problems of stack compression may be further complicated in high-pressure electrochemical cell stacks, because high-pressure operation may cause increased separation of the cells. Thus, a cost-effective, compact, and lightweight system of compression is needed. Further, a system is needed that is capable of maintaining compression in an electrochemical cell stack over an extended period of time and under a range of operating conditions.
- The present disclosure is directed toward the design of improved compression systems for use with electrochemical cells. In particular, the present disclosure is directed towards the design of adjustable compression structures for use with electrochemical cells. Such devices may be used in electrochemical cells operating under high differential pressures, including, but not limited to hydrogen compressors, fuel cells, electrolysis cells, hydrogen purifiers, and hydrogen expanders.
- Embodiments of the present disclosure are directed to a system for applying compressive force to electrochemical cell stacks.
- In accordance with one embodiment, an electrochemical cell stack compression system may include an integral, hollow frame configured to contain a plurality of electrochemical cells arranged along an axis in a stack configuration, wherein the frame has a defined shape and forms a continuous border around a periphery of the electrochemical cell stack when inserted, and wherein the frame is formed of a plurality of fibers.
- Various embodiments of the disclosure may include one or more of the following aspects: the frame may be formed of a plurality of fibers composed of different materials; the frame may include multiple layers formed of fibers; the frame may include a friction-reducing layer located between at least one of the multiple layers formed of fibers; the frame may include at least two opposing wall surfaces; the frame may be further configured to contain at least one end block located at an end region of the frame; the frame may be further configured to contain at least one compression mechanism configured to apply a compressive force to the electrochemical cell stack; the compression mechanism may include at least one gib; the compression mechanism may be configured to expand when heated; the compression mechanism may include one or more internal drive screws extending between two separate portions, wherein rotating the internal drive screws in one direction moves the two portions further away from each other and rotating the internal drive screws in the opposite direction moves the two portions closer to each other; and the frame may be configured to accommodate multiple different sizes of electrochemical cell stacks.
- In accordance with another embodiment, an electrochemical stack compression system may include a structure having a defined shape that is configured to receive and contain a plurality of electrochemical cells arranged in a series along an axis to form an electrochemical stack and at least one compression mechanism configured to apply a compressive force to the electrochemical stack located adjacent to and along the axis of the electrochemical stack, wherein the structure forms a continuous border surrounding the electrochemical stack and the at least one compression mechanism when contained.
- Various embodiments of the disclosure may include one or more of the following aspects: the compression mechanism may include at least one gib; the compression mechanism may include a block that is configured to expand in response to an increase in temperature; the compression mechanism may include internal drive screws configured to increase the size of the compression mechanism when the internal drive screws are rotated in a first direction and to decrease the size of the compression mechanism when the internal drive screws are rotated in a second direction opposite the first direction; the structure may be formed of wound fibers; the fibers may be non-conductive; the fibers may be carbon; and a height of the structure along the axis of the electrochemical stack may change in response to a load applied by the compression mechanism to the electrochemical stack when receiving the compression mechanism.
- A method of preloading various embodiments of the disclosure may include inserting the electrochemical stack into the structure, inserting the at least one compression mechanism into the structure, configuring the compression mechanism to apply a predetermined load within the compression system, and measuring a change in height of the structure along the axis of the electrochemical stack to determine the load being applied by the compression mechanism.
- Various embodiments of the method may further include: inserting at least one end block into the structure; the compression mechanism may include two gibs and configuring the compression mechanism may include wedging the two gibs against each other; configuring the compression mechanism may include increasing the temperature of the compression system to expand the compression mechanism; and configuring the compression mechanism includes rotating a plurality of internal drive screws to expand the compression mechanism.
- In accordance with another embodiment of the present disclosure, an electrochemical stack compression system may include an integral, hollow structure having a defined shape and formed of a plurality of wound fibers; a plurality of electrochemical cells arranged in a series along an axis to form an electrochemical stack, wherein the electrochemical stack is contained within the structure; at least one end block contained within the structure and located at an end region of the structure; and at least one compression mechanism contained within the structure, wherein the at least one compression mechanism is configured to apply a compressive force to the electrochemical stack, and wherein the electrochemical stack, the at least one end block, and the at least one compression mechanism are contained in series within the structure such that the structure forms a continuous border around and adjacent to a periphery of the electrochemical stack, the at least one end block, and the at least one compression mechanism.
- Various embodiments of the disclosure may include one or more of the following aspects: the fibers may be configured to stretch and contract in response to changes in the compressive force; the at least one compression mechanism may include a gib; and the at least one compression mechanism may be configured to expand.
- Additional objects and advantages of the embodiments will be set forth in part in the description that follows, and in part will be obvious from the description, or may be learned by practice of the embodiments. The objects and advantages of the embodiments will be realized and attained by means of the elements and combinations particularly pointed out in the appended claims.
- It is to be understood that both the foregoing general description and the following detailed description are exemplary and explanatory only and are not restrictive of the invention, as claimed.
- The accompanying drawings, which are incorporated in and constitute a part of this specification, illustrate embodiments of the disclosure, and together with the description, serve to explain the principles of the disclosure.
-
FIG. 1 illustrates an exploded view of an exemplary electrochemical cell, according to an embodiment of the present disclosure. -
FIG. 2A illustrates an exemplary electrochemical cell compression system, according to an embodiment of the present disclosure. -
FIG. 2B illustrates an exemplary electrochemical cell compression system, according to an embodiment of the present disclosure. -
FIG. 2C illustrates a cross-section of the exemplary electrochemical cell compression system ofFIG. 2A . -
FIG. 3A illustrates an exemplary compression mechanism for an electrochemical cell compression system according to an exemplary embodiment of the present disclosure. -
FIG. 3B illustrates an alternative view of the exemplary compression mechanism ofFIG. 3A . -
FIG. 4 illustrates an exemplary compression mechanism for an electrochemical cell compression system according to an exemplary embodiment of the present disclosure. - Reference will now be made in detail to the exemplary embodiments of the present disclosure described below and illustrated in the accompanying drawings. Wherever possible, the same reference numbers will be used throughout the drawings to refer to same or like parts.
- While the present disclosure is described herein with reference to illustrative embodiments of a PEM electrochemical cell employing hydrogen, oxygen, and water, it is understood that the devices and methods of the present disclosure may be employed with various types of electrochemical cells, including, but not limited to hydrogen compressors, fuel cells, electrolysis cells, hydrogen purifiers, and hydrogen expanders. Those having ordinary skill in the art and access to the teachings provided herein will recognize additional modifications, applications, embodiments, and substitution of equivalents that all fall within the scope of the disclosure. Accordingly, the disclosure is not to be considered as limited by the foregoing or following descriptions.
- Other features and advantages and potential uses of the present disclosure will become apparent to someone skilled in the art from the following description of the disclosure, which refers to the accompanying drawings.
-
FIG. 1 depicts an individualelectrochemical cell 10, according to an embodiment of the present disclosure. In the exploded side view shown inFIG. 1 ,cell 10 includes a central,electrolyte membrane 8.Electrolyte membrane 8 may be positioned between ananode 7A and a cathode 7B. Together,electrolyte membrane 8,anode 7A, and cathode 7B may formMEA 3. Hydrogen atoms supplied toanode 7A may be electrochemically split into electrons and protons. The electrons may flow through an electric circuit (not shown) to cathode 7B, generating electricity in the process, while the protons may pass throughelectrolyte membrane 8 to cathode 7B. At cathode 7B, protons may react with electrons and oxygen supplied to cathode 7B to produce water and heat. -
Electrolyte membrane 8 may electrically insulateanode 7A from cathode 7B.Electrolyte membrane 8 may be any suitable membrane, including, e.g., a PEM membrane.Electrolyte membrane 8 may be formed of a pure polymer membrane or a composite membrane, which may include, e.g., silica, heteropolyacids, layered metal phosphates, phosphates, and zirconium phosphates, embedded in a polymer matrix.Electrolyte membrane 8 may be permeable to protons but may not conduct electrons.Anode 7A and cathode 7B may include porous carbon electrodes containing a catalyst. The catalyst material, e.g., platinum or any other suitable material, may speed up the reaction of oxygen and fuel. - The size and shape of
MEA 3 may be increased or decreased depending on the application ofcell 10 and the given load requirements. For example, the thickness, length, or width ofMEA 3 may be adjusted according to the given application and requirements. Additionally, the concentration of catalyst material inanode 7A and cathode 7B may be adjusted according to the given application. The concentration of catalyst material inanode 7A and cathode 7B and the thickness ofelectrolyte membrane 8 may each affect the total thickness ofMEA 3. - In some embodiments,
electrochemical cell 10 may optionally include one or more electrically conductive flow structures 5 on each side ofMEA 3. Flow structures 5 may serve as diffusion media enabling the transport of gases and liquids withincell 10. Flow structures 5 may also promote electrical conduction, aid in the removal of heat and water fromelectrochemical cell 10, and provide mechanical support toelectrolyte membrane 8. Flow structures 5 may include, e.g., flow fields, gas diffusion layers (GDL), or any suitable combination thereof. Flow structures 5 may be formed of “frit”-type sintered metals, layered structures, e.g., screen packs and expanded metals, and three-dimensional porous substrates. An exemplary porous metallic substrate may consist of two distinct layers having different average pore sizes. Such flow structures 5 may be formed of any suitable material, including, e.g., metals or metal alloys, such as, e.g., stainless steel, titanium, aluminum, nickel, iron, and nickel-chrome alloys, or any combination thereof. In addition, flow structures 5 may include a suitable coating, such as a corrosion-resistant coating, like carbon, gold, or titanium-nitride. - The reactant gases on each side of the electrolyte membrane are often present at different pressures, e.g., operating pressures may range from approximately 0 psid to 15,000 psid, creating a pressure differential across
MEA 3. For example, when an electrochemical cell is configured as a hydrogen compressor, the flow structure on the cathode side of the membrane is exposed to higher pressures than the flow structure on the anode side. The pressure differential may create a force onMEA 3 that causesMEA 3 to move away from the high pressure side toward the low pressure side. This movement may cause a reduction in contact pressure and separation of the contacting surface ofMEA 3 from flow structures 5 on the high-pressure side. Reduction in pressure and subsequent separation between the contacting surfaces ofMEA 3 and high-pressure flow structures 5 may reduce the electrical conduction and increase the contact resistance between the two, reducing the efficiency ofelectrochemical cell 10. - Flanking flow structures 5 and
MEA 3,cell 10 may also include twobipolar plates Bipolar plate 2A may be positioned on the high-pressure side, andbipolar plate 2B may be positioned on the low-pressure side ofelectrochemical cell 10.Bipolar plates cell 10 from neighboring electrochemical cells (not shown) in a stack. In some embodiments, two adjacent cells in an electrochemical cell stack may share a common bipolar plate. -
Bipolar plates electrochemical cell 10 by means of exhaust gas.Bipolar plates Bipolar plates -
FIGS. 2A through 2C show exemplary electrochemical cellstack compression systems 20, according to embodiments of the present disclosure. Eachindividual cell 10 may be stacked withincompression system 20 to form anelectrochemical cell stack 11.Stack 11 may be comprised of any suitable number ofcells 10.Stack 11 may be located betweenend blocks stack 11. End blocks 12A, 12B may be formed of any suitable metal, plastic, or ceramic material having adequate compressive strength, e.g., aluminum, steel, stainless steel, cast iron, titanium, polyvinyl chloride, polyethylene, polypropylene, nylon, polyether ether ketone, alumina, or any combination thereof. -
Stack 11 andend blocks structure 15. Awound fiber structure 15 may provide a resilient frame capable of housing a high-pressure electrochemical cell stack without significantly increasing the weight or size of the electrochemical cell system.Structure 15 may form a frame with a defined shape into which stack 11 andend blocks FIG. 2A depicts an elongated, rounded,structure 15, butstructure 15 may be any suitable shape, including, e.g., rectangular, oval, circular, or square. The walls ofstructure 15 may form a continuous border long the periphery ofstack 11 andend blocks structure 15 and may or may not enclose the front and/or back portions ofstack 11 andend blocks End bocks structure 15 may be configured to lie flush with the walls ofstructure 15 on an open face, or the components may be recessed withinstructure 15 or they may protrude fromstructure 15, or any suitable combination thereof. -
Structure 15 may be dimensioned to house end blocks 12A, 12B and stack 11, which may include any suitable number ofelectrochemical cells 10. In some embodiments, the size, e.g., the height H, length L (shown inFIG. 2C ), and/or width, ofstructure 15 may vary, for example,structure 15 may be configured to stretch during pre-loading, as discussed further below.Structure 15 may be dimensioned so as to snugly fit the desired contents, for example,electrochemical stack 11 andend blocks - In some embodiments,
structure 15 may be formed of wound fibers that are capable of stretching and contracting. For example,structure 15 may be formed of wound fibers, such as, e.g., carbon, glass, or aramid (e.g., KEVLAR®) fibers. The fibers may be non-conductive to reduce the likelihood of short-circuiting stack 11. In some embodiments,structure 15 may be formed of metallic fibers, such as, e.g., steel, stainless steel, or aluminum, or alloys, such as Inconel.Structure 15 may be formed of homogenous fibers or a mixture of different fibers. Additionally,structure 15 may be formed with or without an epoxy matrix or other suitable material to bind the fibers together. As is shown inFIG. 2C , the walls ofstructure 15 may have a thickness ct.' The wound fiber material properties, such as, e.g., tensile strength, and wall thickness t may be selected to achieve a desired compressive force onstack 11. The fibers making upstructure 15 may be wound together to form one integral frame unit into which stack 11 and various other components fit. - In some embodiments, such as the one shown in
FIG. 2B ,structure 15 may be formed ofmultiple layers FIG. 2B depicts 3 layers, multi-layered embodiments ofstructure 15 may include any suitable number of layers. Each layer may be formed of homogenous fibers or of a combination of different fibers. The layers may be attached to one another, via, e.g., bonding or fastening mechanisms, or may be unattached and held together through, e.g., friction. Additionally, some layers may be attached while other layers may be unattached. In the multi-layer embodiments,structure 15 may include one or more slip-planes 4 between the layers. Slip-plane 4 may be formed of a separate layer or of a coating on one of the layers, such as, e.g., a polytetrafluoroethylene (e.g., TEFLON®), polyetheretherketone, polyimide, nylon, polyethylene, or polymer layer or coating, or any other suitable friction-reducing material to decrease the friction between the layers. If incorporated, slip-plane 4 may be included between each layer or may be included between fewer than all of the layers. The inclusion of slip-plane 4 may reduce the amount of stress withinstructure 15 andcompression system 20, particularly in embodiments having thicker structure walls. - In some embodiments, end blocks 12A, 12B may be also be configured to fit into
structure 15 so that one or both of end blocks 12A, 12B may move withinstructure 15. For example, end blocks 12A, 12B may be allowed to slip along the walls ofstructure 15. This configuration may decrease the stress instructure 15, which may in turn allow forstructure 15 to incorporate thinner walls. In such embodiments, end blocks 12A, 12B may include a suitable friction reducing material or coating, e.g., polytetrafluoroethylene (e.g., TEFLON®), polyetheretherketone, polyimide, nylon, polyethylene. In other embodiments, end blocks 12A, 12B may be attached to the walls ofstructure 15 or may be otherwise configured so that end blocks 12A, 12B may not slip once inserted intostructure 15. - According to another aspect of the disclosure,
compression system 20 may include one or more gibs to promote uniform compression ofelectrochemical stack 11 withinstructure 15. The gibs may act as a wedge to drive two parallel planes instructure 15 apart as the gibs are wedged together in a direction perpendicular to the two parallel planes. For example, as shown inFIGS. 2A through 2C ,gibs electrochemical cell stack 11 and end block 12A to drivestack 11 and end block 12A apart while maintaining their parallel orientation.Gib 14B may have a flat surface and an opposite, angled surface.Gib 14B may be inserted intostructure 15 so that the flat surface lies adjacent to stack 11 and the angled surface faces upwards.Gib 14B may be oriented so that the upward-facing, angled surface slopes in a downward direction toward the front face ofstructure 15 being loaded.Gib 14A may then be inserted next togib 14B, and the two gibs may be driven together.Gib 14A may also have a flat surface and an opposite, angled surface sloped at an angle complimentary to the sloped surface ofgib 14B. The angled surface ofgib 14A may be inserted adjacent the angled surface ofgib 14B so that the angled surface also slopes in downward direction towards the front face ofstructure 15. Thus, asgib 14A is inserted intostructure 15 and driven against 14B, the complimentary slopes may slide against each other, pushing the flat surfaces ofgibs end block 12A andstack 11.Gib 14A may be inserted intostructure 15 until a desired compressive force is exerted onstack 11. -
Gib 14B may also include a grip portion configured to aid in the insertion and removal ofgibs structure 15. In some embodiments,gib 14B may include one or more gripping mechanism configured to engage the walls ofstructure 15 to reduce movement ofgib 14B asgib 14A is inserted. The gripping mechanisms ofgib 14B may engage an inner surface ofstructure 15 or may extend fromgib 14B and engage an edge and/or outer surface ofstructure 15. For example,FIG. 2A depicts hooks 9 protruding outwards fromgib 14B and engaging the edges of opposite walls ofstructure 15. Hooks 9 may preventgib 14B from sliding further intostructure 15 asgib 14A is inserted.Gib 14B may include any suitable gripping mechanism or combination of gripping mechanisms, such as, e.g., protrusions like pegs or hooks, or textured surfaces to reduce movement asgib 14A is wedged againstgib 14B. The gripping mechanisms may be any suitable size, shape, and orientation. In some embodiments, the thick end ofgib 14B may be constrained against a fixed surface asgib 14A is driven, preventing translation againstcell stack 11. - While two
gibs compression system 20. Additionally,gibs stack 11 andend block 12B, or sets of gibs may be located on either side ofstack 11. -
Gibs Gibs compression system 20. Such a suitable friction reducing material may include, e.g., polytetrafluoroethylene (e.g., TEFLON®), polyetheretherketone, polyimide, nylon, polyethylene, or other lubricious polymer coatings, or any other suitable material. -
Gibs structure 15. For example, in some embodiments, the size and shape ofgibs structure 15.Gibs stack 11, which may be based on the application ofstack 11 and the accompanying output requirements. The size and shape ofgibs stack 11 compared to the size ofstructure 15. For example, thesame size structure 15 may be used to housestacks 11 of different sizes. Thus,larger gibs smaller stacks 11 to apply an appropriate compressive force, and vice versa. -
Gibs system 20, and provide planarity. During assembly, components ofcompression system 20, such asstack 11 andend blocks structure 15. At this time,structure 15 may be “pre-loaded” or pre-stretched to apply a predetermined compressive force to stack 11 in order to maintain contact betweenelectrochemical cells 10. This may be accomplished using compressive mechanisms, such asgibs structure 15 to fill any gaps.Gibs structure 15. Asgibs wound fiber structure 15 may increase, and the fibers may stretch. This may increase the height H ofstructure 15. The amount of expansion ofstructure 15 may depend, at least in part, on the wall thickness t and the types of fibers that make upstructure 15. Measuring the change in height H ofstructure 15 during pre-loading may indicate the compressive force being applied to stack 11 and may allow for more precise control of pre-loading conditions. Thus, when woundfiber structure 15 is used in conjunction with the disclosed compression mechanisms,system 20 may provide a lightweight, low-cost system for accurately and effectively applying a compressive load to stack 11. - During operation, as gas pressure in the stack increases, the compressive loading on
stack 11 may decrease untilcells 10 separate. At this point,structure 15 may begin to stretch more than its pre-loaded value. Thus, ifstack 11 heats up more thanstructure 15 during operation,structure 15 may be forced to stretch more than the pre-loaded value due to differential thermal expansion and the force applied to the stack will increase. Thus, the materials ofstructure 15 and any compressive mechanisms may be selected based on their thermal properties to reduce the potential for loss of compressive force during operation. - In some embodiments,
system 20 may include other compressive mechanisms instead of, or in addition to,gibs FIGS. 3A and 3B , in some embodiments, one or more thermal expansion blocks 21 may be used to apply compression to stack 11.Block 21 may be cooled to a temperature below that ofstack 11. During pre-loading, cooledblock 21 may be inserted intocompression system 20. As the temperature ofblock 21 increases inside ofstructure 15, block 21 may expand, and accordingly, may apply compression to stack 11.Block 21 may be formed of any material or combination of materials having suitable thermal expansion characteristics, such as, e.g., suitable metals, metal alloys, or ceramics. In some embodiments, block 21 may be formed of materials with a higher coefficient of thermal expansion than that ofstructure 15. In such embodiments, asstack 11 and block 21 are brought up to operating temperature (generally between 30 and 100° C.), block 21 may expand more thanstructure 15. Such expansion may result in compressive loading ofstack 11. - One advantage of thermally activated compression mechanisms is that
block 21 may be easier to insert intostructure 15. Insertingblock 21 prior to thermal expansion may reduce the wear and stress on the surrounding components ofcompression system 20. For example, as is shown inFIG. 3A , whenblock 21 is initially inserted during pre-loading, agap 17 may exist incompression system 20. Asblock 21 warms,gap 17 may disappear asblock 21 expands and fills the surrounding space (shown inFIG. 3B ). Oncegap 17 disappears, the continued expansion ofblock 21 may begin to compressstack 11 and apply a compressive load. The thermal properties ofblock 21 may be chosen to impart a desired compressive load based on the size ofstack 11 and the size ofgap 17 instructure 15. It will be understood that whilegap 17 is shown between insertedblock 21 andend block 12A, block 21 may be oriented so thatgap 17 occurs on either side ofblock 21, or on both sides ofblock 21. Further,gap 17 may occur in any region withinstructure 15. - While
block 21 is herein described as the expansion member, one or more ofend blocks gibs thermal expansion block 21 andgibs structure 15. - Other embodiments of the present disclosure may include still other compression mechanisms. As shown in
FIG. 4 , ascrew compression unit 19 with internal drive screws may be used to apply a compressive load.Compression unit 19 may be configured to be removable fromstructure 15 or may be attached to structure 15. As is shown inFIG. 4 , threaded screws 18 may extend from a base 16B ofcompression unit 19. The opposite ends ofscrews 18 may extend into complimentary threaded inlets (not shown) inblock 16A ofcompression unit 19. Rotatingscrews 18 in one direction may causescrews 18 to screw further into the threaded inlets inblock 16A, movingblock 16A closer tobase 16B and decreasing the gap between 16A and 16B. Decreasing the gap between 16A and 16B may reduce the compressive force applied to stack 11. Rotatingscrews 18 in the opposite direction may causescrews 18 to unscrew from the threaded inlets inblock 16A, movingblock 16A away frombase 16B and increasing the gap between 16A and 16B. Increasing the gap between 16A and 16B may increase the compressive force applied to stack 11. During pre-loading,compression unit 19 may be inserted intostructure 15 while there is little or no gap betweenblock 16A andbase 16B. Once inserted, screws 18 may be rotated so as to increase the gap betweenblock 16A andbase 16B in order to apply a desired compressive force to stack 11. - While four
screws 18 are depicted inFIG. 4 , any suitable number of threaded components may be included incompression unit 19. Additionally, the threaded components may be distributed onbase 16B in any suitable arrangement.Screws 18 may be any suitable shape or size and may be formed of any suitable material, for example, any metal, metal alloy, or ceramic. Any number ofcompression units 19 may be incorporated insystem 20, andcompression unit 19 may be used in place of or in addition to either or both ofgibs thermal expansion block 21. Further, in some embodiments,compression unit 19 may also be incorporated into one of the components or compression mechanisms described previously. For example, one or more of end blocks 12A, 12B,gibs - One additional advantage of some of the embodiments of disclosed compression system 20 (aside from the reduction in overall stack size and weight) is that
compression system 20 may accommodate electrochemical stacks of different sizes. By incorporatinggibs thermal expansion block 21, and/orcompression unit 19,structure 15 may be configured to receive electrochemical cell stacks of different sizes with different numbers of electrochemical cells suitable for different applications and output levels. If asmaller stack 11 with fewerelectrochemical cells 10 is contained instructure 15, then larger compression mechanisms or a larger number of or combination of compression mechanisms may be inserted aroundstack 11 during pre-loading to fill any additional space and apply a desired compressive force. Alternatively, if a largerelectrochemical cell stack 11 withmore cells 10 is housed instructure 15, smaller compression mechanisms or fewer compression mechanisms may be inserted aroundstack 11. Accordingly, the samebasic structure 15 may be capable of housing different sized electrochemical cell stacks appropriate for different applications and different output levels. This may reduce manufacturing costs, because onestandard structure 15 may be produced for housing a variety of electrochemical cell stack sizes suitable for a variety of applications. Thus, the same basic technology may produce structures for stacks of various cell counts and sizes. By incorporating different numbers of or different types of compression mechanisms described above, thesame structure 15 may be capable of accommodating a range of operating conditions over an extended period of time. - Additionally, the wall thickness of
structure 15 and the types of fibers selected to formstructure 15 may allowstructure 15 to accommodate a range of electrochemical cell stack sizes. Further, in multi-layer embodiments ofstructure 15,structure 15 may be configured so that one or more of the layers is removable or separable from the other layers. For example, one or more of the layers may be nested within another layer and may be capable of being completely removed from the surrounding layer. In an embodiment like that shown inFIG. 2B ,layer 13A may be nested within and removable fromlayer 13B, for example, and slip-plane 4 may facilitate removal. Depending on the size ofelectrochemical cell stack 11 to be inserted intostructure 15, one or more layers may be removed to adaptstructure 15 to the currently applicable operating conditions. - Application of embodiments described above may improve performance of electrochemical cells, including electrochemical cells operating under high-pressure conditions.
- The many features and advantages of the present disclosure are apparent from the detailed specification, and thus, it is intended by the appended claims to cover all such features and advantages of the present disclosure that fall within the true spirit and scope of the present disclosure. Further, since numerous modifications and variations will readily occur to those skilled in the art, it is not desired to limit the present disclosure to the exact construction and operation illustrated and described, and accordingly, all suitable modifications and equivalents may be resorted to, falling within the scope of the present disclosure.
- Moreover, those skilled in the art will appreciate that the conception upon which this disclosure is based may readily be used as a basis for designing other structures, methods, and systems for carrying out the several purposes of the present disclosure. Accordingly, the claims are not to be considered as limited by the foregoing description.
Claims (16)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US16/133,804 US20190020051A1 (en) | 2013-03-08 | 2018-09-18 | Electrochemical stack compression system |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201361775068P | 2013-03-08 | 2013-03-08 | |
US14/198,317 US10109880B2 (en) | 2013-03-08 | 2014-03-05 | Electrochemical stack compression system |
US16/133,804 US20190020051A1 (en) | 2013-03-08 | 2018-09-18 | Electrochemical stack compression system |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US14/198,317 Division US10109880B2 (en) | 2013-03-08 | 2014-03-05 | Electrochemical stack compression system |
Publications (1)
Publication Number | Publication Date |
---|---|
US20190020051A1 true US20190020051A1 (en) | 2019-01-17 |
Family
ID=50240005
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US14/198,317 Active 2035-02-06 US10109880B2 (en) | 2013-03-08 | 2014-03-05 | Electrochemical stack compression system |
US16/133,804 Abandoned US20190020051A1 (en) | 2013-03-08 | 2018-09-18 | Electrochemical stack compression system |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US14/198,317 Active 2035-02-06 US10109880B2 (en) | 2013-03-08 | 2014-03-05 | Electrochemical stack compression system |
Country Status (10)
Country | Link |
---|---|
US (2) | US10109880B2 (en) |
EP (2) | EP2965378B1 (en) |
JP (2) | JP6609189B2 (en) |
KR (1) | KR20150128826A (en) |
CN (2) | CN105122528B (en) |
AU (2) | AU2014226462B2 (en) |
BR (1) | BR112015017429A2 (en) |
CA (1) | CA2898226A1 (en) |
ES (2) | ES2734527T3 (en) |
WO (1) | WO2014137601A2 (en) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP6646427B2 (en) * | 2015-12-15 | 2020-02-14 | 豊田鉄工株式会社 | Battery case |
GB2563848B (en) * | 2017-06-26 | 2022-01-12 | Ceres Ip Co Ltd | Fuel cell stack assembly |
DE102017215510A1 (en) * | 2017-09-05 | 2019-03-07 | Volkswagen Ag | A method of determining the compressive tensile force acting on a fuel cell stack |
CN212119505U (en) * | 2018-12-30 | 2020-12-11 | 熵零技术逻辑工程院集团股份有限公司 | Compression device |
KR102346856B1 (en) * | 2020-01-15 | 2022-01-04 | 한국에너지기술연구원 | Fastening structure for cell stack of flow type energy storage device |
WO2021201962A1 (en) | 2020-03-31 | 2021-10-07 | Plug Power Inc. | Method and system for electrochemically compressing gaseous hydrogen |
US11746427B2 (en) * | 2021-07-05 | 2023-09-05 | EvolOH, Inc. | Scalable electrolysis cell and stack and method of high-speed manufacturing the same |
Family Cites Families (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH06188023A (en) * | 1992-12-22 | 1994-07-08 | Fuji Electric Co Ltd | Flat plate-shaped solid electrolyte type fuel cell |
JP3505010B2 (en) * | 1995-07-07 | 2004-03-08 | 本田技研工業株式会社 | Fuel cell and its fastening method |
US5789091C1 (en) * | 1996-11-19 | 2001-02-27 | Ballard Power Systems | Electrochemical fuel cell stack with compression bands |
JP2002063929A (en) * | 2000-08-14 | 2002-02-28 | Sony Corp | Stack structure of fuel cell |
US6663996B2 (en) | 2000-12-22 | 2003-12-16 | Ballard Power Systems Inc. | Compression mechanism for an electrochemical fuel cell assembly |
US20030072545A1 (en) * | 2001-10-12 | 2003-04-17 | Fujikura Ltd. | Drop cable and method of fabricating same |
US6862801B2 (en) | 2001-11-30 | 2005-03-08 | Ballard Power Systems Inc. | Systems, apparatus and methods for isolating, compressing and/or retaining the structure of a fuel cell stack |
AT5881U1 (en) * | 2002-05-13 | 2003-01-27 | Zeug Design G M B H | SKATING |
JP2004327125A (en) * | 2003-04-22 | 2004-11-18 | Nissan Motor Co Ltd | External manifold type fuel cell |
JP4944444B2 (en) * | 2004-01-20 | 2012-05-30 | 株式会社日立製作所 | Fuel container for fuel cell |
US20060093890A1 (en) * | 2004-10-29 | 2006-05-04 | Steinbroner Matthew P | Fuel cell stack compression systems, and fuel cell stacks and fuel cell systems incorporating the same |
US7294427B2 (en) * | 2004-12-27 | 2007-11-13 | Fuelcell Energy, Inc. | Manifold gasket accommodating differential movement of fuel cell stack |
FI20055017A7 (en) * | 2005-01-13 | 2006-07-14 | Waertsilae Finland Oy | Arrangement for compressing fuel cells in a fuel cell stack |
DE102006030605A1 (en) * | 2006-07-03 | 2008-01-10 | Webasto Ag | Arrangement with a fuel cell stack and method for clamping a fuel cell stack |
DK1879251T3 (en) * | 2006-07-14 | 2012-09-17 | Topsoee Fuel Cell As | Compression Device, Fast Oxide Fuel Cell Stack, Procedure For Compressing the Fast Oxide Fuel Cell Stack and Its Use |
JP4910707B2 (en) * | 2007-01-05 | 2012-04-04 | トヨタ自動車株式会社 | Fuel cell |
ATE469447T1 (en) * | 2007-01-26 | 2010-06-15 | Topsoe Fuel Cell As | FUEL CELL STACK CLAMP STRUCTURE AND SOLID OXIDE FUEL CELL STACK |
US8007951B2 (en) * | 2007-06-08 | 2011-08-30 | GM Global Technology Operations LLC | Fuel cell compression retention system using compliant strapping |
KR100986456B1 (en) * | 2008-03-04 | 2010-10-08 | 포항공과대학교 산학협력단 | Fuel cell stack fastening device |
AU2010223517B2 (en) | 2009-03-13 | 2014-01-16 | Haldor Topsoe A/S | Compression casing for a fuel cell stack and a method for manufacturing a compression casing for a fuel cell stack |
JP5448116B2 (en) * | 2009-04-01 | 2014-03-19 | エルジー・ケム・リミテッド | Battery module with improved safety |
US9331321B2 (en) * | 2011-03-31 | 2016-05-03 | GM Global Technology Operations LLC | Fabric composite support or enclosure for an automotive battery pack |
EP2546915B1 (en) | 2011-07-11 | 2014-06-11 | Belenos Clean Power Holding AG | Housing assembly for a fuel cell stack |
JP5684665B2 (en) * | 2011-07-13 | 2015-03-18 | 本田技研工業株式会社 | Fuel cell stack |
-
2014
- 2014-02-19 EP EP14709057.5A patent/EP2965378B1/en active Active
- 2014-02-19 CA CA2898226A patent/CA2898226A1/en not_active Abandoned
- 2014-02-19 BR BR112015017429A patent/BR112015017429A2/en not_active Application Discontinuation
- 2014-02-19 AU AU2014226462A patent/AU2014226462B2/en active Active
- 2014-02-19 EP EP19177224.3A patent/EP3557673B1/en active Active
- 2014-02-19 JP JP2015561380A patent/JP6609189B2/en active Active
- 2014-02-19 KR KR1020157027579A patent/KR20150128826A/en not_active Ceased
- 2014-02-19 CN CN201480012808.XA patent/CN105122528B/en active Active
- 2014-02-19 ES ES14709057T patent/ES2734527T3/en active Active
- 2014-02-19 WO PCT/US2014/017195 patent/WO2014137601A2/en active Application Filing
- 2014-02-19 ES ES19177224T patent/ES2837698T3/en active Active
- 2014-02-19 CN CN201910760568.6A patent/CN110429314A/en active Pending
- 2014-03-05 US US14/198,317 patent/US10109880B2/en active Active
-
2018
- 2018-06-20 AU AU2018204418A patent/AU2018204418A1/en not_active Abandoned
- 2018-09-18 US US16/133,804 patent/US20190020051A1/en not_active Abandoned
-
2019
- 2019-10-25 JP JP2019194139A patent/JP2020031062A/en not_active Ceased
Also Published As
Publication number | Publication date |
---|---|
JP2016514351A (en) | 2016-05-19 |
AU2014226462A1 (en) | 2015-10-08 |
BR112015017429A2 (en) | 2017-07-11 |
US20140255817A1 (en) | 2014-09-11 |
ES2837698T3 (en) | 2021-07-01 |
EP2965378A2 (en) | 2016-01-13 |
CA2898226A1 (en) | 2014-09-12 |
CN105122528A (en) | 2015-12-02 |
WO2014137601A3 (en) | 2014-11-06 |
JP2020031062A (en) | 2020-02-27 |
US10109880B2 (en) | 2018-10-23 |
EP2965378B1 (en) | 2019-06-19 |
CN110429314A (en) | 2019-11-08 |
WO2014137601A2 (en) | 2014-09-12 |
JP6609189B2 (en) | 2019-11-20 |
AU2014226462B2 (en) | 2018-03-29 |
ES2734527T3 (en) | 2019-12-10 |
CN105122528B (en) | 2019-09-10 |
KR20150128826A (en) | 2015-11-18 |
AU2018204418A1 (en) | 2018-07-12 |
EP3557673A1 (en) | 2019-10-23 |
EP3557673B1 (en) | 2020-11-25 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US20190020051A1 (en) | Electrochemical stack compression system | |
US10305124B2 (en) | Resilient flow structures for electrochemical cell | |
US7851102B2 (en) | Fuel cell stack compression retention system using overlapping sheets | |
JP7361067B2 (en) | Fuel cell with modular base active area | |
US20130034790A1 (en) | Fuel cell stack having a structural heat exchanger | |
US10727501B2 (en) | Bipolar plate having a polymeric coating | |
EP3591754A1 (en) | Electrochemical hydrogen pump | |
JP4494975B2 (en) | Fuel cell stack | |
US12255361B2 (en) | Fuel cell unit | |
GB2505693A (en) | A proton exchange membrane fuel cell with open pore cellular foam | |
US20230124636A1 (en) | Fuel cell unit | |
Lee et al. | A novel design of a cylindrical portable direct methanol fuel cell | |
WO2013025781A1 (en) | Fuel cell stack having a structural heat exchanger |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AS | Assignment |
Owner name: NUVERA FUEL CELLS, INC., MASSACHUSETTS Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:BLANCHET, SCOTT;DOMIT, EDWARD;LAWRIE, DUNCAN;SIGNING DATES FROM 20130829 TO 20130926;REEL/FRAME:046900/0088 Owner name: NUVERA FUEL CELLS, LLC, MASSACHUSETTS Free format text: CERTIFICATE OF CONVERSION;ASSIGNOR:NUVERA FUEL CELLS, INC.;REEL/FRAME:047569/0821 Effective date: 20150515 |
|
STPP | Information on status: patent application and granting procedure in general |
Free format text: DOCKETED NEW CASE - READY FOR EXAMINATION |
|
STPP | Information on status: patent application and granting procedure in general |
Free format text: NON FINAL ACTION MAILED |
|
STPP | Information on status: patent application and granting procedure in general |
Free format text: NON FINAL ACTION MAILED |
|
STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |
|
AS | Assignment |
Owner name: BANK OF AMERICA, N.A., AS ADMINISTRATIVE AGENT, NORTH CAROLINA Free format text: SUPPLEMENTAL SECURITY AGREEMENT;ASSIGNORS:HYSTER-YALE GROUP, INC.;NUVERA FUEL CELLS, LLC;REEL/FRAME:056970/0230 Effective date: 20210528 |
|
AS | Assignment |
Owner name: BANK OF AMERICA, N.A. (A NATIONAL BANKING INSTITUTION), ILLINOIS Free format text: SECURITY INTEREST;ASSIGNORS:HYSTER-YALE GROUP, INC. (A DELAWARE CORPORATION);NUVERA FUEL CELLS, LLC (A DELAWARE LIMITED LIABILITY COMPANY);REEL/FRAME:057013/0037 Effective date: 20210624 |