US20020160249A1 - Flexible graphite article and fuel cell electrode with enhanced electrical and thermal conductivity - Google Patents
Flexible graphite article and fuel cell electrode with enhanced electrical and thermal conductivity Download PDFInfo
- Publication number
- US20020160249A1 US20020160249A1 US10/105,753 US10575302A US2002160249A1 US 20020160249 A1 US20020160249 A1 US 20020160249A1 US 10575302 A US10575302 A US 10575302A US 2002160249 A1 US2002160249 A1 US 2002160249A1
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- Prior art keywords
- sheet
- channels
- article
- graphite
- assembly
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- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 title claims abstract description 123
- 229910002804 graphite Inorganic materials 0.000 title claims abstract description 112
- 239000010439 graphite Substances 0.000 title claims abstract description 112
- 239000000446 fuel Substances 0.000 title description 17
- 239000002245 particle Substances 0.000 claims abstract description 38
- 239000012530 fluid Substances 0.000 claims abstract description 25
- 239000003014 ion exchange membrane Substances 0.000 claims abstract description 8
- 239000012528 membrane Substances 0.000 claims abstract description 5
- 230000003116 impacting effect Effects 0.000 claims description 7
- 239000000463 material Substances 0.000 description 14
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 13
- 239000007789 gas Substances 0.000 description 10
- 229910052799 carbon Inorganic materials 0.000 description 8
- 239000000835 fiber Substances 0.000 description 8
- 239000007800 oxidant agent Substances 0.000 description 8
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 6
- 238000009792 diffusion process Methods 0.000 description 6
- 230000001590 oxidative effect Effects 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- 239000003054 catalyst Substances 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 229910021382 natural graphite Inorganic materials 0.000 description 5
- 229910017604 nitric acid Inorganic materials 0.000 description 5
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 5
- 238000003825 pressing Methods 0.000 description 5
- -1 webs Chemical compound 0.000 description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
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- 239000002184 metal Substances 0.000 description 4
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 3
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 3
- 229910052794 bromium Inorganic materials 0.000 description 3
- KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 description 3
- 239000011888 foil Substances 0.000 description 3
- AWJWCTOOIBYHON-UHFFFAOYSA-N furo[3,4-b]pyrazine-5,7-dione Chemical compound C1=CN=C2C(=O)OC(=O)C2=N1 AWJWCTOOIBYHON-UHFFFAOYSA-N 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- XTEGARKTQYYJKE-UHFFFAOYSA-M Chlorate Chemical compound [O-]Cl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-M 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 2
- 238000005411 Van der Waals force Methods 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
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- 230000015572 biosynthetic process Effects 0.000 description 2
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- 239000001257 hydrogen Substances 0.000 description 2
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- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 2
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- KMUONIBRACKNSN-UHFFFAOYSA-N potassium dichromate Chemical compound [K+].[K+].[O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O KMUONIBRACKNSN-UHFFFAOYSA-N 0.000 description 2
- 239000012286 potassium permanganate Substances 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- QLOKJRIVRGCVIM-UHFFFAOYSA-N 1-[(4-methylsulfanylphenyl)methyl]piperazine Chemical compound C1=CC(SC)=CC=C1CN1CCNCC1 QLOKJRIVRGCVIM-UHFFFAOYSA-N 0.000 description 1
- 229910052582 BN Inorganic materials 0.000 description 1
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 238000003491 array Methods 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- 235000012241 calcium silicate Nutrition 0.000 description 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
- 230000001427 coherent effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
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- 230000008878 coupling Effects 0.000 description 1
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- 238000005859 coupling reaction Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- IQDXNHZDRQHKEF-UHFFFAOYSA-N dialuminum;dicalcium;dioxido(oxo)silane Chemical compound [Al+3].[Al+3].[Ca+2].[Ca+2].[O-][Si]([O-])=O.[O-][Si]([O-])=O.[O-][Si]([O-])=O.[O-][Si]([O-])=O.[O-][Si]([O-])=O IQDXNHZDRQHKEF-UHFFFAOYSA-N 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 235000015250 liver sausages Nutrition 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910001507 metal halide Inorganic materials 0.000 description 1
- 150000005309 metal halides Chemical class 0.000 description 1
- 239000002557 mineral fiber Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- KHIWWQKSHDUIBK-UHFFFAOYSA-N periodic acid Chemical class OI(=O)(=O)=O KHIWWQKSHDUIBK-UHFFFAOYSA-N 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- VKJKEPKFPUWCAS-UHFFFAOYSA-M potassium chlorate Chemical compound [K+].[O-]Cl(=O)=O VKJKEPKFPUWCAS-UHFFFAOYSA-M 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
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- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/50—Constituents or additives of the starting mixture chosen for their shape or used because of their shape or their physical appearance
- C04B2235/52—Constituents or additives characterised by their shapes
- C04B2235/5208—Fibers
- C04B2235/5264—Fibers characterised by the diameter of the fibers
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/60—Aspects relating to the preparation, properties or mechanical treatment of green bodies or pre-forms
- C04B2235/608—Green bodies or pre-forms with well-defined density
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M2300/00—Electrolytes
- H01M2300/0017—Non-aqueous electrolytes
- H01M2300/0065—Solid electrolytes
- H01M2300/0082—Organic polymers
-
- 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
- H01M8/02—Details
- H01M8/0202—Collectors; Separators, e.g. bipolar separators; Interconnectors
- H01M8/0258—Collectors; Separators, e.g. bipolar separators; Interconnectors characterised by the configuration of channels, e.g. by the flow field of the reactant or coolant
- H01M8/026—Collectors; Separators, e.g. bipolar separators; Interconnectors characterised by the configuration of channels, e.g. by the flow field of the reactant or coolant characterised by grooves, e.g. their pitch or depth
-
- 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
-
- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2918—Rod, strand, filament or fiber including free carbon or carbide or therewith [not as steel]
-
- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2927—Rod, strand, filament or fiber including structurally defined particulate matter
-
- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/30—Self-sustaining carbon mass or layer with impregnant or other layer
Definitions
- the present invention relates to an article useful in an electrode assembly for an electrochemical fuel cell.
- the inventive assembly includes an article formed of flexible graphite sheet that is fluid permeable and has enhanced isotropy with respect to thermal and electrical conductivity.
- Graphites are made up of layer planes of hexagonal arrays or networks of carbon atoms. These layer planes of hexagonally arranged carbon atoms are substantially flat and are oriented or ordered so as to be substantially parallel and equidistant to one another.
- the substantially flat, parallel equidistant sheets or layers of carbon atoms usually referred to as basal planes, are linked or bonded together and groups thereof are arranged in crystallites.
- Highly ordered graphites consist of crystallites of considerable size: the crystallites being highly aligned or oriented with respect to each other and having well ordered carbon layers. In other words, highly ordered graphites have a high degree of preferred crystallite orientation.
- graphites possess anisotropic structures and thus exhibit or possess many properties that are highly directional, especially thermal and electrical conductivity and fluid diffusion.
- graphites may be characterized as laminated structures of carbon, that is, structures consisting of superposed layers or laminae of carbon atoms joined together by weak van der Waals forces.
- two axes or directions are usually noted, to wit, the “c” axis or direction and the “a” axes or directions.
- the “c” axis or direction may be considered as the direction perpendicular to the carbon layers.
- the “a” axes or directions may be considered as the directions parallel to the carbon layers or the directions perpendicular to the “c” direction.
- the natural graphites suitable for manufacturing flexible graphite possess a very high degree of orientation.
- the bonding forces holding the parallel layers of carbon atoms together are only weak van der Waals forces.
- Graphites can be treated so that the spacing between the superposed carbon layers or laminae can be appreciably opened up so as to provide a marked expansion in the direction perpendicular to the layers, that is, in the “c” direction and thus form an expanded or intumesced graphite structure in which the laminar character of the carbon layers is substantially retained.
- Natural graphite flake which has been greatly expanded and more particularly expanded so as to have a final thickness or “c” direction dimension which is at least about 80 or more times the original “c” direction dimension can be formed without the use of a binder into cohesive or integrated flexible graphite sheets of expanded graphite, e.g. webs, papers, strips, tapes, or the like.
- the formation of graphite particles which have been expanded to have a final thickness or “c” dimension which is at least about 80 times the original “c” direction dimension into integrated flexible sheets by compression, without the use of any binding material is believed to be possible due to the excellent mechanical interlocking, or cohesion which is achieved between the voluminously expanded graphite particles.
- the sheet material has also been found to possess a high degree of anisotropy with respect to thermal and electrical conductivity and fluid diffusion, comparable to the natural graphite starting material due to orientation of the expanded graphite particles substantially parallel to the opposed faces of the sheet resulting from very high compression, e.g. roll pressing.
- Sheet material thus produced has excellent flexibility, good strength and a very high degree of orientation.
- the process of producing flexible, binderless anisotropic graphite sheet material comprises compressing or compacting under a predetermined load and in the absence of a binder, expanded graphite particles which have a “c” direction dimension which is at least about 80 times that of the original particles so as to form a substantially flat, flexible, integrated graphite sheet.
- the expanded graphite particles which generally are worm-like or vermiform in appearance, once compressed, will maintain the compression set and alignment with the opposed major surfaces of the sheet.
- the density and thickness of the sheet material can be varied by controlling the degree of compression.
- the density of the sheet material can be within the range of from about 5 pounds per cubic foot to about 125 pounds per cubic foot.
- the flexible graphite sheet material exhibits an appreciable degree of anisotropy due to the alignment of graphite particles parallel to the major opposed, parallel surfaces of the sheet, with the degree of anisotropy increasing upon roll pressing of the sheet material to increased density.
- the thickness, i.e. the direction perpendicular to the opposed, parallel sheet surfaces comprises the “c” direction and the directions ranging along the length and width, i.e. along or parallel to the opposed, major surfaces comprises the “a” directions and the thermal, electrical and fluid diffusion properties of the sheet are very different, by orders of magnitude, for the “c” and “a” directions.
- the resistivity of anisotropic flexible graphite sheet is high in the direction transverse to the major surfaces (“c” direction) of the flexible graphite sheet, and very substantially less in the direction parallel to and between the major faces of the flexible graphite sheet (“a” direction).
- c major surfaces
- a major faces of the flexible graphite sheet
- the thermal conductivity of a flexible graphite sheet in a direction parallel to the upper and lower surfaces of the flexible graphite sheet is relatively high, while it is relatively very low in the “c” direction transverse to the upper and lower surfaces.
- a membrane electrode assembly for an electro-chemical fuel cell comprising a pair of electrodes and an ion exchange membrane positioned between the electrodes, at least one of the electrodes being formed of a sheet of a compressed mass of expanded graphite particles having a plurality of transverse fluid channels passing through the sheet between first and second opposed surfaces of the sheet, one of the opposed surfaces abutting the ion exchange membrane.
- the transverse fluid channels are formed by mechanically impacting an opposed surface of the sheet to displace graphite within the sheet at predetermined locations.
- the transverse fluid channels are adjacently positioned and separated by walls of compressed expanded graphite at least some of which permit interconnection between adjacent channels (such as by having grooves therein) to enable fluid flow therebetween.
- FIG. 1 is a plan view of a transversely permeable sheet of flexible graphite having interconnected transverse channels in accordance with the present invention
- FIG. 1(A) shows a flat-ended protrusion element used in making the channels in the perforated sheet of FIG. 1;
- FIG. 2 is a side elevation view in section of the sheet of FIG. 1;
- FIGS. 2 (A), (B), (C) show various suitable flat-ended configurations for transverse interconnected channels in accordance with the present invention
- FIGS. 3 , 3 (A), 3 (B) show a mechanism for making the article of FIG. 1;
- FIGS. 3 (C), 3 (D) show enlarged perspective views of portions of transversely permeable flexible graphite sheet in accordance with the present invention
- FIG. 3(E) is a photograph of a portion of transversely permeable flexible graphite sheet corresponding to FIG. 3(C);
- FIG. 4 shows an enlarged sketch of an elevation view of the oriented expanded graphite particles of flexible graphite sheet material
- FIG. 5 is a sketch of an enlarged elevation view of an article formed of flexible graphite sheet in accordance with the present invention.
- FIG. 5, 6, 7 and 7 (A) show a fluid permeable electrode assembly which includes a transversely permeable article in accordance with the present invention.
- FIG. 8 is a photograph at 100 ⁇ (original magnification) corresponding to a portion of the side elevation view sketch of FIG. 5.
- Graphite is a crystalline form of carbon comprising atoms covalently bonded in flat layered planes with weaker bonds between the planes.
- an intercalant of, for instance, a solution of sulfuric and nitric acid
- the treated particles of graphite are hereafter referred to as “particles of intercalated graphite”.
- the particles of intercalated graphite Upon exposure to high temperature, the particles of intercalated graphite expand in dimension as much as about 80 or more times its original volume in an accordion-like fashion in the “c” direction, i.e., in the direction perpendicular to the crystalline planes of the graphite.
- the exfoliated graphite particles are vermiform in appearance, and are therefore commonly referred to as worms.
- the worms may be compressed together into flexible sheets that, unlike the original graphite flakes, can be formed and cut into various shapes and provided with small transverse openings by deforming mechanical impact.
- a common method for manufacturing graphite sheet, e.g., foil from flexible graphite is described by Shane et al. in U.S. Pat. No. 3,404,061, the disclosure of which is incorporated herein by reference.
- natural graphite flakes are intercalated by dispersing the flakes in a solution containing an oxidizing agent of, for example, a mixture of nitric and sulfuric acid.
- the intercalation solution contains oxidizing and other intercalating agents known in the art.
- Examples include those containing oxidizing agents and oxidizing mixtures, such as solutions containing nitric acid, potassium chlorate, chromic acid, potassium permanganate, potassium chromate, potassium dichromate, perchloric acid, and the like, or mixtures, such as for example, concentrated nitric acid and chlorate, chromic acid and phosphoric acid, sulfuric acid and nitric acid, or mixtures of a strong organic acid, such as trifluoroacetic acid, and a strong oxidizing agent soluble in the organic acid.
- oxidizing agents and oxidizing mixtures such as solutions containing nitric acid, potassium chlorate, chromic acid, potassium permanganate, potassium chromate, potassium dichromate, perchloric acid, and the like, or mixtures, such as for example, concentrated nitric acid and chlorate, chromic acid and phosphoric acid, sulfuric acid and nitric acid, or mixtures of a strong organic acid, such as trifluoroacetic acid, and
- the intercalating agent is a solution of a mixture of sulfuric acid, or sulfuric acid and phosphoric acid, and an oxidizing agent, i.e., nitric acid, perchloric acid, chromic acid, potassium permanganate, hydrogen peroxide, iodic or periodic acids, or the like.
- the intercalation solutions may contain metal halides such as ferric chloride, and ferric chloride mixed with sulfuric acid, or a halide, such as bromine as a solution of bromine and sulfuric acid or bromine in an organic solvent.
- any excess solution is drained from the flakes and the flakes are water-washed.
- the quantity of intercalation solution retained on the flakes after draining may range from 20 to 150 parts of solution by weight per 100 parts by weight of graphite flakes (pph) and more typically about 50 to 120 pph.
- the quantity of the intercalation solution may be limited to between 10 to 50 parts of solution per hundred parts of graphite by weight (pph) which permits the washing step to be eliminated as taught and described in U.S. Pat. No. 4,895,713, the disclosure of which is also herein incorporated by reference.
- the thus treated particles of graphite are sometimes referred to as “particles of intercalated graphite”.
- the particles of intercalated graphite Upon exposure to high temperature, e.g. up to about 700° C. to 1000° C. and higher, the particles of intercalated graphite expand as much as about 80 to 1000 or more times its original volume in an accordion-like fashion in the c-direction, i.e., in the direction perpendicular to the crystalline planes of the constituent graphite particles.
- the expanded (or exfoliated) graphite particles are vermiform in appearance, and are therefore commonly referred to as worms.
- the worms may be compressed together into flexible sheets that, unlike the original graphite flakes, can be formed and cut into various shapes and provided with small transverse openings by deforming mechanical impact as hereinafter described.
- Flexible graphite sheet and foil are coherent, with good handling strength, and are suitably compressed, such as by roll-pressing, to a thickness of 0.003 to 0.15 inch and a density of 0.1 to 1.5 grams per cubic centimeter.
- ceramic additives can be blended with the intercalated graphite flakes as described in U.S. Pat. No. 5,902,762 (which is incorporated herein by reference) to provide enhanced resin impregnation in the final flexible graphite product.
- the additives include ceramic fiber particles having a length of 0.15 to 1.5 millimeters. The width of the particles is suitably from 0.04 to 0.004 mm.
- the ceramic fiber particles are non-reactive and non-adhering to graphite and are stable at temperatures up to 2000° F., preferably 2500° F..
- Suitable ceramic fiber particles are formed of macerated quartz glass fibers, carbon and graphite fibers, zirconia, boron nitride, silicon carbide and magnesia fibers, naturally occurring mineral fibers such as calcium metasilicate fibers, calcium aluminum silicate fibers, aluminum oxide fibers and the like.
- a compressed mass of expanded graphite particles, in the form of a flexible graphite sheet is shown at 10 .
- the flexible graphite sheet 10 is provided with channels 20 , which are preferably smooth-sided as indicated at 67 in FIGS. 5 and 8, and which pass between the parallel, opposed surfaces 30 , 40 of flexible graphite sheet 10 , and are separated by walls 3 of compressed expandable graphite.
- the walls 3 are advantageously provided with grooves 5 , having a depth of ⁇ fraction (1/10) ⁇ to 1 ⁇ 3 the depth of the channels in accordance with the present invention.
- the channels 20 preferably have openings 50 on one of the opposed surfaces 30 which are larger than the openings 60 in the other opposed surface 40 .
- the channels 20 can have different configurations as shown at 20 ′- 20 ′′′′ in FIGS. 2 (A), 2 (B), 2 (C) which are formed using flat-ended protrusion elements of different shapes as shown at 75 , 175 , 275 , 375 in FIGS. 1 (A) and 2 (A), 2 (B), 2 (C), 2 (D), suitably formed of metal, e.g. steel, and integral with and extending from the pressing roller 70 of the impacting device shown in FIG. 3.
- metal e.g. steel
- the groove-forming protrusion elements 675 , 775 , 875 , 975 also result in deformation and displacement of graphite within the flexible graphite sheet.
- Preferred channel-forming protrusion elements 77 have decreasing cross-section in the direction away from the pressing roller 70 to provide larger channel openings on the side of the sheet which is initially impacted.
- the development of smooth, unobstructed surfaces 63 surrounding channel openings 60 enables the free flow of fluid into and through smooth-sided (at 67 ) channels 20 .
- openings at one of the opposed surfaces are larger than the channel openings in the other opposed surface, e.g. from 1 to 200 times greater in area, and result from the use of protrusion elements having converging sides such as shown at 76 , 276 , 376 .
- the transverse channels 20 are formed in the flexible graphite sheet 10 at a plurality of pre-determined locations by mechanical impact at the predetermined locations in sheet 10 using a mechanism such as shown in FIG. 3 comprising a pair of steel rollers 70 , 72 with one of the rollers having truncated, i.e.
- channel-forming protrusions 75 which impact surface 30 of flexible graphite sheet 10 to displace graphite and penetrate sheet 10 to form open channels 20 .
- the channel-forming protrusions 75 are bridged by groove-forming protrusions 675 which form interconnecting grooves 5 between channels 20 in a row of aligned channels concurrently with formation of channels 20 which is illustrated in the sketch of FIG. 3(C) and the photograph of FIG. 3(E).
- groove-forming protrusion elements 675 ′ can be included as shown in FIGS. 3 (A), 3 (B) to form interconnecting grooves 5 ′ in a parallel row of transverse channels 20 as shown in FIG. 3(D).
- both rollers 70 , 72 can be provided with “out-of-register” protrusions, and a flat metal plate indicated at 79 , can be used in place of smooth-surfaced roller 72 .
- FIG. 4 is an enlarged sketch of a sheet of flexible graphite 110 that shows a typical prior art orientation of compressed expanded graphite particles 80 substantially parallel to the opposed surfaces 130 , 140 .
- This orientation of the expanded graphite particles 80 results in anisotropic properties in flexible graphite sheets; i.e. the electrical conductivity and thermal conductivity of the sheet is substantially lower in the direction transverse to opposed surfaces 130 , 140 (“c ” direction) than in the direction (“a” direction) parallel to opposed surfaces 130 , 140 .
- the perforated gas permeable flexible graphite sheet 10 of FIG. 1 can be used as an electrode in an electrochemical fuel cell 500 shown schematically in FIGS. 6, 7 and 7 (A).
- FIG. 6, FIG. 7 and FIG. 7(A) show, schematically, the basic elements of an electrochemical Fuel Cell, more complete details of which are disclosed in U.S. Pat. Nos. 4,988,583 and 5,300,370 and PCT WO 95/16287 (Jun. 15, 1995) and each of which is incorporated herein by reference.
- the Fuel Cell indicated generally at 500 comprises electrolyte in the form of a plastic e.g. a solid polymer ion exchange membrane 550 catalyst coated at surfaces 601 , 603 , e.g. coated with platinum 600 as shown in FIG. 7(A); perforated flexible graphite sheet electrodes 10 in accordance with the present invention; and flow field plates 1000 , 1100 which respectively abut electrodes 10 .
- Pressurized fuel is circulated through grooves 1400 of fuel flow field pate 1100 and pressurized oxidant is circulated through grooves 1200 .
- the fuel flow field plate 1100 becomes an anode
- the oxidant flow field plate 1000 becomes a cathode with the result that an electric potential, i.e. voltage is developed between the fuel flow field plate 1000 and the oxidant flow field plate 1100 .
- the above described electrochemical fuel cell is combined with others in a fuel cell stack to provide the desired level of electric power as described in the above-noted U.S. Pat. No. 5,300,370.
- fluid from adjacent channels can flow through grooves 5 so that gas-catalyst contact adjacent the blocked channel is maintained.
- the initial velocity of the gas at the smaller openings 60 is higher than the gas flow at the larger openings 50 with the result that the gas is slowed down when it contacts the catalyst 600 and the residence time of gas-catalyst contact is increased and the area of gas exposure at the membrane 550 is maximized.
- FIG. 8 is a photograph (original magnification 100 ⁇ ) of a body of flexible graphite corresponding to a portion of the sketch of FIG. 5.
- FIGS. 1 and 5 and the material shown in the photograph (100 ⁇ ) of FIG. 8 can be shown to have increased thermal and electrical conductivity in the direction transverse to opposed parallel, planar surfaces 30 , 40 as compared to the thermal and electrical conductivity in the direction transverse to surfaces 130 , 140 of the material of FIG. 4 in which particles of expanded natural graphite unaligned with the opposed planar surfaces are not optically detectable.
- transverse gas permeability of channeled flexible graphite sheet samples was measured, using a Gurley Model 4118 for Gas Permeability Measurement.
- the preferred channel density is from 1000 to 3000 channels per square inch and the preferred channel size is a channel in which the ratio of the area of larger channel opening to the smaller is from 50:1 to 150:1.
- the flexible graphite sheet can, at times, be advantageously treated with resin and the absorbed resin, after curing, enhances the moisture resistance and handling strength, i.e. stiffness of the flexible graphite sheet.
- Suitable resin content is preferably 20 to 30% by weight, suitably up 60% by weight.
- the article of the present invention can be used as electrical and thermal coupling elements for integrated circuits in computer applications, as conformal electrical contact pads and as electrically energized grids in de-icing equipment.
Abstract
A graphite article useful in producing a membrane electrode assembly comprising a pair of electrodes and an ion exchange membrane positioned between the electrodes is presented. At least one of the electrodes is formed of a sheet of a compressed mass of expanded graphite particles having a plurality of transverse fluid channels passing through the sheet between first and second opposed surfaces of the sheet, one of opposed surfaces abutting the ion exchange membrane when used in a membrane electrode assembly. At least some of the fluid channels are interconnected to enable flow of fluid therebetween.
Description
- The present invention relates to an article useful in an electrode assembly for an electrochemical fuel cell. The inventive assembly includes an article formed of flexible graphite sheet that is fluid permeable and has enhanced isotropy with respect to thermal and electrical conductivity.
- Graphites are made up of layer planes of hexagonal arrays or networks of carbon atoms. These layer planes of hexagonally arranged carbon atoms are substantially flat and are oriented or ordered so as to be substantially parallel and equidistant to one another. The substantially flat, parallel equidistant sheets or layers of carbon atoms, usually referred to as basal planes, are linked or bonded together and groups thereof are arranged in crystallites. Highly ordered graphites consist of crystallites of considerable size: the crystallites being highly aligned or oriented with respect to each other and having well ordered carbon layers. In other words, highly ordered graphites have a high degree of preferred crystallite orientation. It should be noted that graphites possess anisotropic structures and thus exhibit or possess many properties that are highly directional, especially thermal and electrical conductivity and fluid diffusion. Briefly, graphites may be characterized as laminated structures of carbon, that is, structures consisting of superposed layers or laminae of carbon atoms joined together by weak van der Waals forces. In considering the graphite structure, two axes or directions are usually noted, to wit, the “c” axis or direction and the “a” axes or directions. For simplicity, the “c” axis or direction may be considered as the direction perpendicular to the carbon layers. The “a” axes or directions may be considered as the directions parallel to the carbon layers or the directions perpendicular to the “c” direction. The natural graphites suitable for manufacturing flexible graphite possess a very high degree of orientation.
- As noted above, the bonding forces holding the parallel layers of carbon atoms together are only weak van der Waals forces. Graphites can be treated so that the spacing between the superposed carbon layers or laminae can be appreciably opened up so as to provide a marked expansion in the direction perpendicular to the layers, that is, in the “c” direction and thus form an expanded or intumesced graphite structure in which the laminar character of the carbon layers is substantially retained.
- Natural graphite flake which has been greatly expanded and more particularly expanded so as to have a final thickness or “c” direction dimension which is at least about 80 or more times the original “c” direction dimension can be formed without the use of a binder into cohesive or integrated flexible graphite sheets of expanded graphite, e.g. webs, papers, strips, tapes, or the like. The formation of graphite particles which have been expanded to have a final thickness or “c” dimension which is at least about 80 times the original “c” direction dimension into integrated flexible sheets by compression, without the use of any binding material is believed to be possible due to the excellent mechanical interlocking, or cohesion which is achieved between the voluminously expanded graphite particles.
- In addition to flexibility, the sheet material, as noted above, has also been found to possess a high degree of anisotropy with respect to thermal and electrical conductivity and fluid diffusion, comparable to the natural graphite starting material due to orientation of the expanded graphite particles substantially parallel to the opposed faces of the sheet resulting from very high compression, e.g. roll pressing. Sheet material thus produced has excellent flexibility, good strength and a very high degree of orientation.
- Briefly, the process of producing flexible, binderless anisotropic graphite sheet material, such as web, paper, strip, tape, foil, mat, or the like, comprises compressing or compacting under a predetermined load and in the absence of a binder, expanded graphite particles which have a “c” direction dimension which is at least about 80 times that of the original particles so as to form a substantially flat, flexible, integrated graphite sheet. The expanded graphite particles, which generally are worm-like or vermiform in appearance, once compressed, will maintain the compression set and alignment with the opposed major surfaces of the sheet. The density and thickness of the sheet material can be varied by controlling the degree of compression. The density of the sheet material can be within the range of from about 5 pounds per cubic foot to about 125 pounds per cubic foot. The flexible graphite sheet material exhibits an appreciable degree of anisotropy due to the alignment of graphite particles parallel to the major opposed, parallel surfaces of the sheet, with the degree of anisotropy increasing upon roll pressing of the sheet material to increased density. In roll pressed anisotropic sheet material, the thickness, i.e. the direction perpendicular to the opposed, parallel sheet surfaces comprises the “c” direction and the directions ranging along the length and width, i.e. along or parallel to the opposed, major surfaces comprises the “a” directions and the thermal, electrical and fluid diffusion properties of the sheet are very different, by orders of magnitude, for the “c” and “a” directions.
- This very considerable difference in properties, known as anisotropy, which is directionally dependent, can be disadvantageous in some applications. For example, in gasket applications where flexible graphite sheet is used as the gasket material and in use is held tightly between metal surfaces, the diffusion of fluid, e.g. gases or liquids, occurs more readily parallel to and between the major surfaces of the flexible graphite sheet. It would, in most instances, provide for greater gasket performance, if the resistance to fluid flow parallel to the major surfaces of the graphite sheet (“a” direction) were increased, even at the expense of reduced resistance to fluid diffusion flow transverse to the major faces of the graphite sheet (“c” direction). With respect to electrical properties, the resistivity of anisotropic flexible graphite sheet is high in the direction transverse to the major surfaces (“c” direction) of the flexible graphite sheet, and very substantially less in the direction parallel to and between the major faces of the flexible graphite sheet (“a” direction). In applications such as fluid flow field plates for fuel cells and seals for fuel cells, it would be of advantage if the electrical resistance transverse to the major surfaces of the flexible graphite sheet (“c” direction) were decreased, even at the expense of an increase in electrical resistivity in the direction parallel to the major faces of the flexible graphite sheet (“a” direction).
- With respect to thermal properties, the thermal conductivity of a flexible graphite sheet in a direction parallel to the upper and lower surfaces of the flexible graphite sheet is relatively high, while it is relatively very low in the “c” direction transverse to the upper and lower surfaces.
- The foregoing situations are accommodated by the present invention.
- In accordance with the present invention, a membrane electrode assembly for an electro-chemical fuel cell is provided, comprising a pair of electrodes and an ion exchange membrane positioned between the electrodes, at least one of the electrodes being formed of a sheet of a compressed mass of expanded graphite particles having a plurality of transverse fluid channels passing through the sheet between first and second opposed surfaces of the sheet, one of the opposed surfaces abutting the ion exchange membrane. Advantageously, the transverse fluid channels are formed by mechanically impacting an opposed surface of the sheet to displace graphite within the sheet at predetermined locations. The transverse fluid channels are adjacently positioned and separated by walls of compressed expanded graphite at least some of which permit interconnection between adjacent channels (such as by having grooves therein) to enable fluid flow therebetween.
- FIG. 1 is a plan view of a transversely permeable sheet of flexible graphite having interconnected transverse channels in accordance with the present invention;
- FIG. 1(A) shows a flat-ended protrusion element used in making the channels in the perforated sheet of FIG. 1;
- FIG. 2 is a side elevation view in section of the sheet of FIG. 1;
- FIGS.2(A), (B), (C) show various suitable flat-ended configurations for transverse interconnected channels in accordance with the present invention;
- FIGS.3, 3(A), 3(B) show a mechanism for making the article of FIG. 1;
- FIGS.3(C), 3(D) show enlarged perspective views of portions of transversely permeable flexible graphite sheet in accordance with the present invention;
- FIG. 3(E) is a photograph of a portion of transversely permeable flexible graphite sheet corresponding to FIG. 3(C);
- FIG. 4 shows an enlarged sketch of an elevation view of the oriented expanded graphite particles of flexible graphite sheet material;
- FIG. 5 is a sketch of an enlarged elevation view of an article formed of flexible graphite sheet in accordance with the present invention;
- FIG. 5, 6,7 and 7(A) show a fluid permeable electrode assembly which includes a transversely permeable article in accordance with the present invention; and
- FIG. 8 is a photograph at 100× (original magnification) corresponding to a portion of the side elevation view sketch of FIG. 5.
- Graphite is a crystalline form of carbon comprising atoms covalently bonded in flat layered planes with weaker bonds between the planes. By treating particles of graphite, such as natural graphite flake, with an intercalant of, for instance, a solution of sulfuric and nitric acid, the crystal structure of the graphite reacts to form a compound of graphite and the intercalant. The treated particles of graphite are hereafter referred to as “particles of intercalated graphite”. Upon exposure to high temperature, the particles of intercalated graphite expand in dimension as much as about 80 or more times its original volume in an accordion-like fashion in the “c” direction, i.e., in the direction perpendicular to the crystalline planes of the graphite. The exfoliated graphite particles are vermiform in appearance, and are therefore commonly referred to as worms. The worms may be compressed together into flexible sheets that, unlike the original graphite flakes, can be formed and cut into various shapes and provided with small transverse openings by deforming mechanical impact.
- A common method for manufacturing graphite sheet, e.g., foil from flexible graphite is described by Shane et al. in U.S. Pat. No. 3,404,061, the disclosure of which is incorporated herein by reference. In the typical practice of the Shane et al. method, natural graphite flakes are intercalated by dispersing the flakes in a solution containing an oxidizing agent of, for example, a mixture of nitric and sulfuric acid. The intercalation solution contains oxidizing and other intercalating agents known in the art. Examples include those containing oxidizing agents and oxidizing mixtures, such as solutions containing nitric acid, potassium chlorate, chromic acid, potassium permanganate, potassium chromate, potassium dichromate, perchloric acid, and the like, or mixtures, such as for example, concentrated nitric acid and chlorate, chromic acid and phosphoric acid, sulfuric acid and nitric acid, or mixtures of a strong organic acid, such as trifluoroacetic acid, and a strong oxidizing agent soluble in the organic acid.
- In a preferred embodiment, the intercalating agent is a solution of a mixture of sulfuric acid, or sulfuric acid and phosphoric acid, and an oxidizing agent, i.e., nitric acid, perchloric acid, chromic acid, potassium permanganate, hydrogen peroxide, iodic or periodic acids, or the like. Although less preferred, the intercalation solutions may contain metal halides such as ferric chloride, and ferric chloride mixed with sulfuric acid, or a halide, such as bromine as a solution of bromine and sulfuric acid or bromine in an organic solvent.
- After the flakes are intercalated, any excess solution is drained from the flakes and the flakes are water-washed. The quantity of intercalation solution retained on the flakes after draining may range from 20 to 150 parts of solution by weight per 100 parts by weight of graphite flakes (pph) and more typically about 50 to 120 pph. Alternatively, the quantity of the intercalation solution may be limited to between 10 to 50 parts of solution per hundred parts of graphite by weight (pph) which permits the washing step to be eliminated as taught and described in U.S. Pat. No. 4,895,713, the disclosure of which is also herein incorporated by reference. The thus treated particles of graphite are sometimes referred to as “particles of intercalated graphite”. Upon exposure to high temperature, e.g. up to about 700° C. to 1000° C. and higher, the particles of intercalated graphite expand as much as about 80 to 1000 or more times its original volume in an accordion-like fashion in the c-direction, i.e., in the direction perpendicular to the crystalline planes of the constituent graphite particles. The expanded (or exfoliated) graphite particles are vermiform in appearance, and are therefore commonly referred to as worms. The worms may be compressed together into flexible sheets that, unlike the original graphite flakes, can be formed and cut into various shapes and provided with small transverse openings by deforming mechanical impact as hereinafter described.
- Flexible graphite sheet and foil are coherent, with good handling strength, and are suitably compressed, such as by roll-pressing, to a thickness of 0.003 to 0.15 inch and a density of 0.1 to 1.5 grams per cubic centimeter. From about 1.5-30% by weight of ceramic additives, can be blended with the intercalated graphite flakes as described in U.S. Pat. No. 5,902,762 (which is incorporated herein by reference) to provide enhanced resin impregnation in the final flexible graphite product. The additives include ceramic fiber particles having a length of 0.15 to 1.5 millimeters. The width of the particles is suitably from 0.04 to 0.004 mm. The ceramic fiber particles are non-reactive and non-adhering to graphite and are stable at temperatures up to 2000° F., preferably 2500° F.. Suitable ceramic fiber particles are formed of macerated quartz glass fibers, carbon and graphite fibers, zirconia, boron nitride, silicon carbide and magnesia fibers, naturally occurring mineral fibers such as calcium metasilicate fibers, calcium aluminum silicate fibers, aluminum oxide fibers and the like.
- With reference to FIG. 1 and FIG. 2, a compressed mass of expanded graphite particles, in the form of a flexible graphite sheet is shown at10. The
flexible graphite sheet 10 is provided withchannels 20, which are preferably smooth-sided as indicated at 67 in FIGS. 5 and 8, and which pass between the parallel,opposed surfaces flexible graphite sheet 10, and are separated bywalls 3 of compressed expandable graphite. Thewalls 3 are advantageously provided withgrooves 5, having a depth of {fraction (1/10)} to ⅓ the depth of the channels in accordance with the present invention. Thechannels 20 preferably haveopenings 50 on one of the opposed surfaces 30 which are larger than theopenings 60 in the otheropposed surface 40. Thechannels 20 can have different configurations as shown at 20′-20″″ in FIGS. 2(A), 2(B), 2(C) which are formed using flat-ended protrusion elements of different shapes as shown at 75, 175, 275, 375 in FIGS. 1(A) and 2(A), 2(B), 2(C), 2(D), suitably formed of metal, e.g. steel, and integral with and extending from thepressing roller 70 of the impacting device shown in FIG. 3. The smooth flat-ends of the channel-formingprotrusion elements protrusion elements smooth bearing surface 73, ofroller 70, and the smooth bearing surface 78 of roller 72 (or alternatively flat metal plate 79), ensure deformation and displacement of graphite within the flexible graphite sheet, preferably such that there are no rough or ragged edges or debris resulting from the channel-forming impact. The groove-formingprotrusion elements protrusion elements 77 have decreasing cross-section in the direction away from thepressing roller 70 to provide larger channel openings on the side of the sheet which is initially impacted. The development of smooth,unobstructed surfaces 63 surroundingchannel openings 60, enables the free flow of fluid into and through smooth-sided (at 67)channels 20. - In a preferred embodiment, openings at one of the opposed surfaces are larger than the channel openings in the other opposed surface, e.g. from 1 to 200 times greater in area, and result from the use of protrusion elements having converging sides such as shown at76, 276, 376. The
transverse channels 20 are formed in theflexible graphite sheet 10 at a plurality of pre-determined locations by mechanical impact at the predetermined locations insheet 10 using a mechanism such as shown in FIG. 3 comprising a pair ofsteel rollers protrusions 75 which impact surface 30 offlexible graphite sheet 10 to displace graphite and penetratesheet 10 to formopen channels 20. In the present invention, the channel-formingprotrusions 75 are bridged by groove-formingprotrusions 675 which form interconnectinggrooves 5 betweenchannels 20 in a row of aligned channels concurrently with formation ofchannels 20 which is illustrated in the sketch of FIG. 3(C) and the photograph of FIG. 3(E). Additionally, groove-formingprotrusion elements 675′ can be included as shown in FIGS. 3(A), 3(B) to form interconnectinggrooves 5′ in a parallel row oftransverse channels 20 as shown in FIG. 3(D). In practice, bothrollers roller 72. FIG. 4 is an enlarged sketch of a sheet offlexible graphite 110 that shows a typical prior art orientation of compressed expandedgraphite particles 80 substantially parallel to theopposed surfaces graphite particles 80 results in anisotropic properties in flexible graphite sheets; i.e. the electrical conductivity and thermal conductivity of the sheet is substantially lower in the direction transverse toopposed surfaces 130, 140 (“c ” direction) than in the direction (“a” direction) parallel toopposed surfaces flexible graphite sheet 10 to formchannels 20, as illustrated in FIG. 3, graphite is displaced withinflexible graphite sheet 10 by flat-ended (at 77) channel-formingprotrusions 75 to push aside graphite as it travels to and bears againstsmooth surface 73 ofroller 70 to disrupt and deform the parallel orientation of expandedgraphite particles 80 as shown at 800 in FIG. 5. Groove formingprotrusions 675 concurrently deform the parallel orientation of expanded graphite particles. This region of 800,adjacent channels 20 andgrooves 5, shows disruption of the parallel orientation into an oblique, non-parallel orientation is optically observable at magnifications of 100× and higher. In effect the displaced graphite is being “die-molded” by thesides 76 ofadjacent protrusions 75 and thesmooth surface 73 ofroller 70 as illustrated in FIG. 5. This reduces the anisotropy inflexible graphite sheet 10 and thus increases the electrical and thermal conductivity ofsheet 10 in the direction transverse to the opposed surfaces 30, 40. A similar effect is achieved with frusto-conical and parallel-sided peg-shaped flat-endedprotrusions 275 and 175. The perforated gas permeableflexible graphite sheet 10 of FIG. 1 can be used as an electrode in anelectrochemical fuel cell 500 shown schematically in FIGS. 6, 7 and 7(A). - FIG. 6, FIG. 7 and FIG. 7(A) show, schematically, the basic elements of an electrochemical Fuel Cell, more complete details of which are disclosed in U.S. Pat. Nos. 4,988,583 and 5,300,370 and PCT WO 95/16287 (Jun. 15, 1995) and each of which is incorporated herein by reference.
- With reference to FIG. 6, FIG. 7 and FIG. 7(A), the Fuel Cell indicated generally at500, comprises electrolyte in the form of a plastic e.g. a solid polymer
ion exchange membrane 550 catalyst coated atsurfaces platinum 600 as shown in FIG. 7(A); perforated flexiblegraphite sheet electrodes 10 in accordance with the present invention; and flowfield plates electrodes 10. Pressurized fuel is circulated throughgrooves 1400 of fuelflow field pate 1100 and pressurized oxidant is circulated throughgrooves 1200. In operation, the fuelflow field plate 1100 becomes an anode, and the oxidantflow field plate 1000 becomes a cathode with the result that an electric potential, i.e. voltage is developed between the fuelflow field plate 1000 and the oxidantflow field plate 1100. The above described electrochemical fuel cell is combined with others in a fuel cell stack to provide the desired level of electric power as described in the above-noted U.S. Pat. No. 5,300,370. - The operation of
Fuel Cell 500 requires that theelectrodes 10 be porous to the fuel and oxidant fluids, e.g. hydrogen and oxygen, to permit these components to readily pass from thegrooves electrodes 10 to contact thecatalyst 600, as shown in FIG. 7(A), and enable protons derived from hydrogen to migrate throughion exchange membrane 550. In theelectrode 10 of the present invention,channels 20 are positioned to adjacentlycover grooves smaller openings 60 ofchannels 20 and exits thelarger openings 50 ofchannels 20. In the event of a blockage in achannel 20, such as indicated at 7 in FIGS. 6 and 7, fluid from adjacent channels can flow throughgrooves 5 so that gas-catalyst contact adjacent the blocked channel is maintained. The initial velocity of the gas at thesmaller openings 60 is higher than the gas flow at thelarger openings 50 with the result that the gas is slowed down when it contacts thecatalyst 600 and the residence time of gas-catalyst contact is increased and the area of gas exposure at themembrane 550 is maximized. This feature, together with the increased electrical conductivity of the flexible graphite electrode of the present invention enables more efficient fuel cell operation. - FIG. 8 is a photograph (original magnification 100×) of a body of flexible graphite corresponding to a portion of the sketch of FIG. 5.
- The articles of FIGS. 1 and 5 and the material shown in the photograph (100×) of FIG. 8 can be shown to have increased thermal and electrical conductivity in the direction transverse to opposed parallel,
planar surfaces surfaces - A sample of a sheet of flexible graphite 0.01 inch thick having a density of 0.3 grams/cc, representative of FIG. 4, was mechanically impacted by a device similar to that of FIG. 3 to provide channels of different size in the flexible graphite sheet. The transverse (“c” direction) electrical resistance of the sheet material samples was measured and the results are shown in the table below.
- Also, the transverse gas permeability of channeled flexible graphite sheet samples, in accordance with the present invention, was measured, using a Gurley Model 4118 for Gas Permeability Measurement.
- Samples of channeled flexible graphite sheet in accordance with the present invention were placed at the bottom opening (⅜ in. diam.) of a vertical cylinder (3 inch diameter cross-section). The cylinder was filled with 300 cc of air and a weighted piston (5 oz.) was set in place at the top of the cylinder. The rate of gas flow through the channeled samples was measured as a function of the time of descent of the piston and the results are shown in the table below.
Flexible Graphite Sheet (0.01 inch thick; density = 0.3 gms/cc) 1600 channels per 250 channels per square inch—0.020 square inch—0.020 inch wide at top; inch wide at top; No 0.005 inch wide at 0.007 inch wide at Channels bottom bottom Transverse 80 8 0.3 Electrical Resistance (micro ohms) Diffusion Rate- — 8 seconds 30 seconds Seconds - In the present invention, for a flexible graphite sheet having a thickness of 0.003 inch to 0.015 inch adjacent the channels and a density of 0.5 to 1.5 grams per cubic centimeter, the preferred channel density is from 1000 to 3000 channels per square inch and the preferred channel size is a channel in which the ratio of the area of larger channel opening to the smaller is from 50:1 to 150:1.
- In the practice of the present invention, the flexible graphite sheet can, at times, be advantageously treated with resin and the absorbed resin, after curing, enhances the moisture resistance and handling strength, i.e. stiffness of the flexible graphite sheet. Suitable resin content is preferably 20 to 30% by weight, suitably up 60% by weight.
- The article of the present invention can be used as electrical and thermal coupling elements for integrated circuits in computer applications, as conformal electrical contact pads and as electrically energized grids in de-icing equipment.
- The above description is intended to enable the person skilled in the art to practice the invention. It is not intended to detail all of the possible variations and modifications which will become apparent to the skilled worker upon reading the description. It is intended, however, that all such modifications and variations be included within the scope of the invention which is defined by the following claims. The claims are intended to cover the indicated elements and steps in any arrangement or sequence which is effective to meet the objectives intended for the invention, unless the context specifically indicates the contrary.
Claims (20)
1. A membrane electrode assembly comprising a pair of electrodes and an ion exchange membrane positioned between the electrodes, at least one of the electrodes being formed of a sheet of a compressed mass of expanded graphite particles having a plurality of transverse fluid channels passing through the sheet between first and second opposed surfaces thereof and separated by walls of compressed expanded graphite particles, at least some of the walls permitting interconnection of adjacent channels, one of the opposed surfaces abutting the ion exchange membrane.
2. The assembly of claim 1 wherein the transverse fluid channels are formed by mechanically impacting an opposed surface of the sheet to displace graphite within the sheet at a plurality of predetermined locations.
3. The assembly of claim 1 wherein interconnection of at least some of the adjacent channels is permitted by grooves formed in at least some of the walls.
4. The assembly of claim 3 wherein the interconnecting grooves are formed by mechanically impacting an opposed surface of the sheet at walls separating adjacent channels to enable fluid flow between adjacent channels.
5. The assembly of claim 1 wherein the compressed mass of expanded graphite particles is characterized by expanded graphite particles adjacent said channels extending obliquely with respect to opposed surfaces of the sheet.
6. The assembly of claim 1 wherein the channel openings at the second surface of the sheet are surrounded by a smooth graphite surface.
7. The assembly of claim 1 wherein the channel openings at the first surface are larger than the channel openings at the second surface.
8. The assembly of claim 7 wherein the channel openings at the first surface are from 50 to 150 times larger in area than the channel openings at the second surface.
9. The assembly of claim 1 wherein 1000 to 3000 channels per square inch are present in the sheet.
10. The assembly of claim 1 wherein the graphite sheet has a thickness of 0.003 inch to 0.015 inch adjacent said channels and a density of 0.5 to 1.5 grams per cubic centimeter.
11. A graphite article comprising a sheet of a compressed mass of expanded graphite particles having a plurality of transverse fluid channels passing through the sheet between first and second opposed surfaces thereof and separated by walls of compressed expanded graphite particles, at least some of the walls permitting interconnection of adjacent channels.
12. The article of claim 11 wherein the transverse fluid channels are formed by mechanically impacting an opposed surface of the sheet to displace graphite within the sheet at a plurality of predetermined locations.
13. The article of claim 11 wherein interconnection of at least some of the adjacent channels is permitted by grooves formed in at least some of the walls.
14. The article of claim 13 wherein the interconnecting grooves are formed by mechanically impacting an opposed surface of the sheet at walls separating adjacent channels to enable fluid flow between adjacent channels.
15. The article of claim 11 wherein the compressed mass of expanded graphite particles is characterized by expanded graphite particles adjacent said channels extending obliquely with respect to opposed surfaces of the sheet.
16. The article of claim 11 wherein the channel openings at the second surface of the sheet are surrounded by a smooth graphite surface.
17. The article of claim 11 wherein the channel openings at the first surface are larger than the channel openings at the second surface.
18. The article of claim 17 wherein the channel openings at the first surface are from 50 to 150 times larger in area than the channel openings at the second surface.
19. The article of claim 11 wherein 1000 to 3000 channels per square inch are present in the sheet.
20. The article of claim 11 wherein the graphite sheet has a thickness of 0.003 inch to 0.015 inch adjacent said channels and a density of 0.5 to 1.5 grams per cubic centimeter.
Priority Applications (2)
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US10/105,753 US20020160249A1 (en) | 2000-04-10 | 2002-03-25 | Flexible graphite article and fuel cell electrode with enhanced electrical and thermal conductivity |
US10/273,756 US20030108731A1 (en) | 2000-01-24 | 2002-10-18 | Molding of fluid permeable flexible graphite components for fuel cells |
Applications Claiming Priority (2)
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US09/545,956 US6413671B1 (en) | 2000-04-10 | 2000-04-10 | Flexible graphite article and fuel cell electrode with enhanced electrical and thermal conductivity |
US10/105,753 US20020160249A1 (en) | 2000-04-10 | 2002-03-25 | Flexible graphite article and fuel cell electrode with enhanced electrical and thermal conductivity |
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US09/549,865 Continuation US6528199B1 (en) | 2000-01-24 | 2000-04-14 | Graphite article useful as an electrode for an electrochemical fuel cell |
US09/675,027 Continuation US6479182B1 (en) | 2000-01-24 | 2000-09-28 | Fuel cell electrode assembly with selective catalyst loading |
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US10/273,756 Continuation-In-Part US20030108731A1 (en) | 2000-01-24 | 2002-10-18 | Molding of fluid permeable flexible graphite components for fuel cells |
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Cited By (1)
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US20080014493A1 (en) * | 2006-07-05 | 2008-01-17 | Samsung Sdi Co., Ltd. | Fuel cell having water recirculation plate |
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