WO2006049005A1 - 電極用導電材の前駆フェルト材および電極用導電材の製造法 - Google Patents
電極用導電材の前駆フェルト材および電極用導電材の製造法 Download PDFInfo
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- WO2006049005A1 WO2006049005A1 PCT/JP2005/018948 JP2005018948W WO2006049005A1 WO 2006049005 A1 WO2006049005 A1 WO 2006049005A1 JP 2005018948 W JP2005018948 W JP 2005018948W WO 2006049005 A1 WO2006049005 A1 WO 2006049005A1
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- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/36—Accumulators not provided for in groups H01M10/05-H01M10/34
- H01M10/39—Accumulators not provided for in groups H01M10/05-H01M10/34 working at high temperature
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/64—Carriers or collectors
- H01M4/70—Carriers or collectors characterised by shape or form
- H01M4/80—Porous plates, e.g. sintered carriers
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- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/42—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
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- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/44—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties the fleeces or layers being consolidated by mechanical means, e.g. by rolling
- D04H1/46—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties the fleeces or layers being consolidated by mechanical means, e.g. by rolling by needling or like operations to cause entanglement of fibres
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- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/44—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties the fleeces or layers being consolidated by mechanical means, e.g. by rolling
- D04H1/46—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties the fleeces or layers being consolidated by mechanical means, e.g. by rolling by needling or like operations to cause entanglement of fibres
- D04H1/498—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties the fleeces or layers being consolidated by mechanical means, e.g. by rolling by needling or like operations to cause entanglement of fibres entanglement of layered webs
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- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/70—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres characterised by the method of forming fleeces or layers, e.g. reorientation of fibres
- D04H1/74—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres characterised by the method of forming fleeces or layers, e.g. reorientation of fibres the fibres being orientated, e.g. in parallel (anisotropic fleeces)
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/64—Carriers or collectors
- H01M4/66—Selection of materials
- H01M4/663—Selection of materials containing carbon or carbonaceous materials as conductive part, e.g. graphite, carbon fibres
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/64—Carriers or collectors
- H01M4/70—Carriers or collectors characterised by shape or form
- H01M4/80—Porous plates, e.g. sintered carriers
- H01M4/801—Sintered carriers
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/64—Carriers or collectors
- H01M4/70—Carriers or collectors characterised by shape or form
- H01M4/80—Porous plates, e.g. sintered carriers
- H01M4/806—Nonwoven fibrous fabric containing only fibres
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/86—Inert electrodes with catalytic activity, e.g. for fuel cells
- H01M4/96—Carbon-based electrodes
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- 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
- Y02E60/10—Energy storage using batteries
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- 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
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- 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
- Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
- Y10T428/24942—Structurally defined web or sheet [e.g., overall dimension, etc.] including components having same physical characteristic in differing degree
- Y10T428/24992—Density or compression of components
Definitions
- the present invention relates to a precursor felt material for an electrode conductive material that can hold a large amount of electrode material such as molten sulfur due to a large number of voids, and a method for producing a conductive material for an electrode composed of low-density carbon fiber felt About.
- a fuel cell is a system that extracts hydrogen by electrochemically reacting hydrogen extracted from natural gas and other oxygen with oxygen in the air. Waste heat of about 100 ° C generated during power generation is used to supply hot water and heat.
- the phosphoric acid aqueous solution type is suitable for small-scale private power generation.
- Na-S batteries are common, and in the case of Na-S batteries, a carbon material for supplying electrons to sulfur is used as the anode.
- This carbon material is suitable as an auxiliary material for an electrode because it generally exhibits high electronic conductivity, is scientifically inert, and does not react with substances.
- PAN-based flame-resistant fiber felt to improve conductive properties and reduce the contact resistance between each member, and further uses ⁇ -alumina powder on the surface of carbon fiber felt. It is sprayed.
- PAN-based carbon fiber felts are If used alone, there is a limit to improving battery performance as a conductive material for electrodes, and a sufficient improvement in performance is possible even if alumina powder is sprayed.
- JP-A-11-158737, JP-A-2000-306587, and JP-A-2001-115369 pay attention to a flame-resistant fiber felt before it is made into carbon fiber felt by high-temperature firing. This is done for the flame-resistant fiber felt as a precursor.
- a flameproof fiber alone or a mixture of flameproof fiber and carbon fiber is carbonized at a maximum temperature of 1100 ° C or higher to convert it into carbon fiber with a high carbonization yield.
- a carbon fiber felt obtained by densely punching from one or both sides of a flame-resistant fiber wrap to have a fiber alignment degree in the thickness direction of 20% or more is obtained by using ordinary carbon fiber felt. It has the necessary conductivity and high heat resistance as an anode conductive material with less problems of clogging than fiber felt.
- Japanese Patent Laid-Open No. 001-115369 a flameproof fiber web was weakened, a preliminary felt was formed by needle punching, and the web was further laminated on one or both sides of the preliminary felt to obtain a force-one dollar punching.
- the carbon fiber felt material has a high bulk density and high mechanical strength, and has a great increase in the amount of fibers arranged in the thickness direction, resulting in excellent electrical conductivity.
- Patent Document 1 Japanese Patent Laid-Open No. 8-130032
- Patent Document 2 Japanese Patent Laid-Open No. 11-158737
- Patent Document 3 Japanese Patent Laid-Open No. 2000-306587
- Patent Document 4 Japanese Patent Laid-Open No. 2001-115369
- the flame-resistant fiber felt as a precursor is much more flexible than a carbon fiber felt, and thus can be subjected to almost a desired one-dollar punching process. It is possible to obtain a carbon fiber felt that is somewhat bulky by orienting the felt fiber in the thickness direction.
- the fact is that the flame-resistant fibers are drastically drooped by the dense-single-punch process, so there is a limit to reducing the density of the carbon fiber felt, and that the felt density will increase to some extent. It cannot be avoided.
- these conductive materials for electrodes still remain inside the anode when used in Na-S batteries. There is considerable resistance to inhibit the active material reaction, and it cannot be said that the molten sulfur content in the electrode material is sufficient.
- the present invention has been proposed in order to improve the above-mentioned problems associated with conventional electrode conductive materials, and reduces the amount of relatively expensive flame-resistant fibers used and increases the firing efficiency.
- a precursor felt material for a conductive material is provided.
- Another object of the present invention is to provide a method for producing a conductive material for an electrode having a lower felt density and more voids than a normal carbon fiber felt.
- the method for producing an electrode conductive material according to the present invention a relatively large amount of flame-resistant fibers and a relatively small amount of organic fibers are mixed to form a wrap, and the fibers are oriented in the thickness direction by needle punching. To make the laminated wrap felt. Thereafter, the obtained felt material is baked at 1100 to 2000 ° C. to carbonize the flameproof fiber, and the organic fiber is burned to almost evaporate the solids. To lower the felt density to produce a low-density electrode conductive material.
- the felt density of the conductive material for an electrode is desirably 0.065-0.107 gZcm 3 , more preferably 0.077-0.lOOgZcm 3 .
- the precursor felt material according to the present invention is used for firing a low density electrode conductive material having a felt density of 0.065-0.107 gZcm 3 and an electric resistance of 1 to 500 ⁇ .
- the precursor felt material of the present invention is formed by blending 70 to 98% by weight of flame-resistant fiber and 2 to 30% by weight of organic fiber to form a wrap, and then finely punching one or both sides of the laminated wrap.
- the fibers are oriented in the thickness direction, the density is 0.120-0.155 gZcm 3 , and the degree of fiber alignment in the thickness direction is 30% or more.
- 90 to 95% by weight of flame-resistant fiber and 5 to 10% by weight of organic fiber are blended.
- the flameproof fiber is a PAN-based fiber
- the organic fiber is a polyolefin, polyamide or polyester fiber
- the polyolefin fiber is more preferably a polypropylene fiber.
- the polypropylene fiber which is an organic fiber
- the fiber length of organic fibers ranges from 5 mm to the length of flame-resistant fibers. More preferably, it is between 10 mm and the length of the flameproofing fiber to 10 mm minus V.
- An electrode conductive material 1 (Fig. 2) according to the present invention is substantially composed of a carbon fiber felt, and the precursor felt material 2 shown in Fig. 1 is formed at 1100 to 2000 ° C. Manufactured by firing.
- the electrode conductive material 1 can be used for, for example, a secondary battery such as a Na—S battery 3 (FIG. 3) or a fuel cell.
- This fuel cell includes a phosphoric acid aqueous solution type with a power generation efficiency of 40%, an internal reforming molten carbonate type with a power generation efficiency of 50%, and a fixed electrolyte type with a large-scale power source.
- a Na-S battery 3 as an example of a secondary battery is mainly used in an electric power storage system, and is arranged in a cylindrical anode container 5 and in the center of the anode container as illustrated in FIG.
- the solid electrolyte tube has a bottomed cylindrical shape and is selectively permeable to Na ions.
- a molten metal sodium container 7 having an opening at the bottom is disposed inside the solid electrolyte tube 6, a molten metal sodium container 7 having an opening at the bottom is disposed.
- the electrode conductive material 1 that is the anode conductive material 9 is impregnated with molten sulfur and curved in a cylindrical shape, and is disposed between the outer peripheral surface of the solid electrolyte tube 6 and the inner peripheral surface of the anode container 5.
- molten metal sodium discharges electrons to become Na ions during discharge, and Na ions permeate the solid electrolyte tube 6 and move to the anode side, and the conductive material 1 for electrodes.
- V and Na ions react with sulfur and electrons that have passed through an external circuit to produce sodium polysulfate, generating a voltage of about 2V.
- polysulfuric acid sodium is divided into Na ions, sulfur, and electrons, and Na ions pass through the solid electrolyte tube 6 and move to the cathode side, receive electrons, and return to sodium.
- a large number of Na-S batteries 3 are installed in a prismatic battery module, for example, so that the output is 4 kW.
- the battery module is composed of 25 units in 5 series and 5 in parallel. To do.
- a relatively large amount of flame-resistant fiber 8 and a relatively small amount of organic fiber 10 are mixed to form a wrap, and the fiber is formed by dense needle punching.
- the laminated wrap is felted by orienting in the thickness direction.
- the flame resistant fiber is 70-98% by weight and the organic fiber is 2-30% by weight, preferably the flame resistant fiber is 90-95% by weight and the organic fiber is 5-10% by weight.
- Organic fiber is not 2% by weight If it is full, it is difficult to uniformly disperse both fibers, and if it exceeds 30% by weight, the firing efficiency decreases.
- the precursor felt material 2 is! /
- the flame-resistant fiber 8 is a normal PAN-based fiber! / ⁇ .
- the flameproof fiber 8 is a precursor for producing carbon fiber, and is also called black soot fiber or carbon oxide fiber.
- Flame-resistant fibers are basically flame-resistant, that is, heat-stabilized by ladder polymerization by the formation of naphthyridine rings.
- the fiber properties of flame-resistant fiber 8 are as follows: density 1.3 to 1.5 gZcm 3 , tensile strength 1. OgZ decitex or higher, elongation 10% or higher, fineness 1.5 to 4.0 dtex, crimp rate 8% or higher It is. With the flame resistant fiber 8 having such physical properties, it is possible to produce an electrode conductive material having a low internal resistance after blending with a relatively small amount of the organic fiber 10 and punching and firing.
- the relatively small amount of the organic fiber 10 may be polyolefin, polyamide, or polyester fiber that is not particularly limited in its type.
- the organic fiber 10 is preferably a polypropylene fiber because it is easily baked and has less residue after baking, and the polyolefin fiber is desired to be felt.
- the fineness of the organic fiber 10 is preferably 3 to 22 dtex, preferably 6 to 15 dtex! If the fineness of the fiber is less than 3 decitex, it becomes difficult to secure a gap in the electrode conductive material as soon as the felt is lost, and if it exceeds 22 decitex, the size of the void in the electrode conductive material tends to vary.
- the fiber length of the organic fiber 10 is between 5 mm and the length of the flame-resistant fiber 8, and more so that the 10 mm force is also between the length of the flame-resistant fiber minus 10 mm. preferable. If the fiber length of the organic fiber 10 is less than 5 mm, it will fall off without entanglement with the flame-resistant fiber 8 and if the fiber length exceeds the length of the flame-resistant fiber 8, the fiber will become too entangled and the felt will break. Therefore, the felt density is not sufficiently reduced.
- the flameproof fiber 8 and the organic fiber 10 are mixed to form a wrap by carding or the like.
- This lapping force can also produce the desired precursor felt material ( Figure 1).
- Precursor felt material 2 is manufactured by finely punching one-sided or double-sided force of the obtained wrap, and as shown in Fig. 2, this -one-dollar punching causes fiber 10 to move in the thickness direction. Orient.
- the electrode conductive material 1 The one-dollar punch surface is positioned on the solid electrolyte tube side.
- the number of needle punches is varied for each felt surface, and a finer one-dollar punch surface is positioned on the solid electrolyte tube side.
- Precursor felt material 2 dense - one US dollar defines the fiber alignment of the thickness direction by punching 3 0% or more, preferably the density is 0. 120-0 155gZcm 3.. When the fiber arrangement is less than 30%, a clogging problem occurs in a Na—S battery or the like, and it is difficult to immediately reduce the internal resistance of the battery. Generally, the thickness of the precursor felt material 2 is about 120 to 145% of the predetermined electrode thickness, and the thickness of about 17 mm is reduced by about 2 mm by firing.
- the electrode conductive material 1 is obtained by firing the precursor felt material 2 at 1100 to 2000 ° C., that is, carbonizing. When the precursor felt material 2 is baked at 1100 to 2000 ° C., the organic fibers 10 in the felt material are burned and the solid content thereof is almost evaporated, and the organic fiber 10 is voided to reduce the felt density. Electrode conductive material 1, the air gap of the organic fiber sections, the Fuenoreto density force ⁇ ). Dropped to 065-0. 107 g / cm 3, becomes preferably ⁇ or 0. 077 ⁇ 0. 100g / cm 3 .
- the electrode conductive material 1 When used for the Na-S battery 3 (Fig. 3), the electrode conductive material 1 is appropriately cut and curved into a cylindrical shape, and the outer peripheral surface of the solid electrolyte tube 6 and the inner peripheral surface of the anode container 5 Place between.
- the electrode conductive material 1 has necessary conductivity by firing after dense-one-dollar punching, even if the precursor felt material 2 is an electrically insulating material.
- the electrode conductive material 1 exhibits the high heat resistance necessary for firing even if the flameproof fiber 8 of the precursor felt material 2 has only about 300 ° C. heat resistance.
- the conductive material for electrodes obtained by the method of the present invention has a lower felt density and more voids than ordinary carbon fiber felts, so that it can be used for secondary batteries such as Na-S batteries or fuel cells. If used, electrode materials such as molten sulfur can be impregnated in a larger amount, and the power generation efficiency is dramatically improved.
- This electrode conductive material has a large number of voids between fibers and a high degree of fiber alignment, so that when used in a secondary battery, the problem of clogging is less likely to occur compared to ordinary carbon fiber felt. When to use internal resistance such as Na-S battery Reduce.
- the cost of the electrode conductive material can be reduced because the amount of the relatively expensive flame-resistant fiber is small. wear.
- the presence of organic fibers combusted at the time of firing increases the firing efficiency of the conductive material for electrodes, and this also reduces the cost considerably.
- FIG. 1 is an enlarged cross-sectional view schematically showing a precursor felt material according to the present invention.
- FIG. 2 is an enlarged cross-sectional view schematically showing a conductive material for an electrode produced by the method of the present invention.
- FIG. 3 is a schematic cross-sectional view showing a Na—S battery for a power storage system, which is an example of using an electrode conductive material.
- ⁇ ? ⁇ -Based flame-resistant fiber 8 produced by firing acrylic fiber at 200-300 in an active atmosphere such as air to produce conductive material 1 for electrodes (eg, trade name: Neurometas, Toho Tenax)
- This PAN-based flameproof fiber 8 is a short fiber having a fineness of 2.2 dtex and a fiber length of 51 mm.
- the PAN-based flameproof fiber 8 is mixed with 10% by weight of polypropylene short fibers having a fineness of 11 dtex and a fiber length of 32 mm, and a wrap is formed by carding in a known card machine. A predetermined number of the obtained wraps are laminated, and a precursor felt material 2 having a density of 0.148 gZcm 3 and a fiber arrangement degree of 38% is produced from one side by needle punching. [0027] The precursor felt material 2 is further baked at about 1600 ° C to carbonize the flame-resistant fiber 8 and burn the polypropylene short fiber to almost evaporate the solid content. The portion of the polypropylene short fiber in the glass was voided to obtain a felt-like electrode conductive material 1.
- the density of the conductive material 1 for electrodes was further reduced to 0.095 gZcm 3 .
- This conductive material for electrodes 1 has a lower felt density and more voids than ordinary carbon fiber felt, and can be impregnated with a larger amount of molten sulfur when used in Na-S batteries. The power generation efficiency of the battery increases.
- the PAN-based flameproof fiber 8 used in Example 1 was mixed with 10% by weight of polypropylene short fiber having a fineness of 7.7 decitex and a fiber length of 32 mm, and was carded by a known card machine. Form a wrap. A predetermined number of the obtained wraps are laminated, and a precursor felt material 2 having a density of 0.148 gZcm 3 and a fiber arrangement degree of 38% is produced from one side by needle punching.
- the precursor felt material 2 is further baked at about 1600 ° C to carbonize the flame-resistant fiber 8 and burn the polypropylene short fiber to almost evaporate the solid content.
- the portion of the polypropylene short fiber in the glass was voided to obtain a felt-like electrode conductive material 1.
- the density of the conductive material 1 for an electrode was further reduced to 0.099 gZcm 3 .
- This conductive material for electrodes 1 has a lower felt density and more voids than ordinary carbon fiber felt, and can be impregnated with a larger amount of molten sulfur when used in Na-S batteries. The power generation efficiency of the battery increases.
- the PAN-based flameproof fiber 8 used in Example 1 is mixed with 5% by weight of polypropylene short fibers having a fineness of 4.4 dtex and a fiber length of 30 mm.
- a precursor felt material 2 having a density of 0.154 gZcm 3 and a fiber arrangement degree of 33% is produced by the same treatment as in Example 1.
- the precursor felt material 2 carbonizes the flame-resistant fiber 8 by firing, burns the polypropylene short fiber to substantially evaporate the solid content, voids the portion of the polypropylene short fiber in the felt material 2, and the felt.
- the electrode-shaped conductive material 1 was obtained. Electrode conductive material 1 is The density of this was 0. lOlgZcm 3 . This conductive material for electrodes 1 has a lower felt density and more voids than ordinary carbon fiber felt, and when used in Na-S batteries, it can be impregnated with a larger amount of molten sulfur. Increases efficiency.
- the PAN-based flameproof fiber 8 used in Example 1 is mixed with 10% by weight of polyester fiber having a fineness of 6.6 dtex and a fiber length of 38 mm instead of polypropylene short fiber.
- a precursor felt material 2 having a density of 0.142 gZcm 3 and a fiber arrangement degree of 31% is produced by the same treatment as in Example 1.
- the precursor felt material 2 carbonizes the flameproof fiber 8 by firing, burns the polyester fiber to substantially evaporate the solid content, voids the polyester fiber portion of the felt material 2, and forms a felt-like electrode.
- Conductive material 1 was obtained.
- the electrode conductive material 1 had a density of 0.095 gZcm 3 .
- This conductive material for electrodes 1 has a lower felt density and more voids than ordinary carbon fiber felt, and when used in Na-S batteries, it can impregnate a larger amount of molten sulfur. Is up.
- the same PAN-based flameproof fiber as in Example 1 is used, and a wrap of 100% PAN-based flameproof fiber is formed.
- processing is performed in substantially the same manner as in Example 1, but the number of punches per dollar is increased, and a precursor felt material having a density of 0.173 g / cm 3 and a fiber arrangement degree of 42% is manufactured.
- the precursor felt material is carbonized by firing to obtain a felt-shaped electrode conductive material.
- the obtained electrode conductive material had a density of 0.115 gZcm 3 .
- This conductive material for electrodes has a slightly lower felt density than ordinary carbon fiber felts but has fewer voids.
- the amount of molten sulfur impregnated is almost the same as in the past. The power generation efficiency has hardly improved.
- Example 2 In order to produce the precursor felt material, the same PAN-based flameproof fiber as in Example 1 is used, and a wrap of 100% PAN-based flameproof fiber is formed. Next, it is processed in substantially the same manner as in Example 1, except that the number of punches per dollar is reduced, the density is 0.155 gZcm 3 and the fiber arrangement is 23%. Produce a pre-fault material.
- the precursor felt material is carbonized by firing to obtain a felt-shaped electrode conductive material.
- the obtained conductive material for electrodes had a density of 0.1 lOgZcm 3 .
- This conductive material for electrodes has a slightly lower felt density than ordinary carbon fiber felts but has fewer voids.
- the amount of molten sulfur impregnated is almost the same as in the past. The power generation efficiency has hardly improved.
- the precursor felt material is carbonized by firing to obtain a felt-shaped electrode conductive material.
- the obtained conductive material for electrodes had a density of 0.1OOgZcm 3 .
- This conductive material for electrodes has a long polypropylene fiber, so that the entanglement of the fiber is too much and the felt is sunk, and the felt density reduction is somewhat insufficient. Even if this conductive material for electrodes is lower than normal carbon fiber felt and has a felt density, the amount of impregnation of molten sulfur is the same as before when used in Na-S batteries, and the power generation efficiency of Na-S batteries is Do not up.
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- Electrochemistry (AREA)
- Textile Engineering (AREA)
- Mechanical Engineering (AREA)
- Materials Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Secondary Cells (AREA)
- Battery Electrode And Active Subsutance (AREA)
- Nonwoven Fabrics (AREA)
- Cell Electrode Carriers And Collectors (AREA)
- Carbon And Carbon Compounds (AREA)
Abstract
Description
Claims
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11/666,897 US7501109B2 (en) | 2004-11-04 | 2005-10-14 | Method for manufacturing an electric conductor for electrodes |
EP05793235.2A EP1855346B1 (en) | 2004-11-04 | 2005-10-14 | Precursor felt for electroconductive material for electrode and method for producing electroconductive material for electrode |
JP2006542943A JP4531768B2 (ja) | 2004-11-04 | 2005-10-14 | 電極用導電材の前駆フェルト材および電極用導電材の製造法 |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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JP2004320092 | 2004-11-04 | ||
JP2004-320092 | 2004-11-04 |
Publications (1)
Publication Number | Publication Date |
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WO2006049005A1 true WO2006049005A1 (ja) | 2006-05-11 |
Family
ID=36319019
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2005/018948 WO2006049005A1 (ja) | 2004-11-04 | 2005-10-14 | 電極用導電材の前駆フェルト材および電極用導電材の製造法 |
Country Status (6)
Country | Link |
---|---|
US (1) | US7501109B2 (ja) |
EP (1) | EP1855346B1 (ja) |
JP (1) | JP4531768B2 (ja) |
KR (1) | KR101209098B1 (ja) |
CN (1) | CN100486028C (ja) |
WO (1) | WO2006049005A1 (ja) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20090011673A1 (en) * | 2007-07-03 | 2009-01-08 | Feng Chia University | Porous carbonized fabric with high efficiency and its preparation method and uses |
WO2009128215A1 (ja) * | 2008-04-14 | 2009-10-22 | 東洋炭素株式会社 | 炭素繊維炭素複合成形体及び炭素繊維強化炭素複合体材料並びにその製造方法 |
JP2014167173A (ja) * | 2013-02-28 | 2014-09-11 | Toray Ind Inc | 炭素繊維不織布の製造方法および不織布 |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TWI347992B (en) * | 2007-09-03 | 2011-09-01 | Univ Feng Chia | Carbonized paper with high strength and its preparation method and uses |
CN101463521B (zh) * | 2007-12-19 | 2011-09-28 | 逢甲大学 | 高性能多孔性碳化织物及其制备方法与用途 |
FR2943257B1 (fr) * | 2009-03-19 | 2011-04-15 | Ferlam Technologies | Bourrelet coupe-feu |
CN102811941B (zh) * | 2009-11-06 | 2016-08-03 | 奥本大学 | 用于优化和控制高放热和高吸热反应/过程的微纤维介质 |
CN103474125B (zh) * | 2013-09-11 | 2016-10-12 | 安顿雷纳(上海)纤维材料科技有限公司 | 一种利用废弃纤维制作的电极材料及其制造方法 |
CN106549161B (zh) * | 2016-12-09 | 2019-06-28 | 大连融科储能技术发展有限公司 | 液流电池电极结构及液流电池电堆 |
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JPH01253163A (ja) * | 1988-03-31 | 1989-10-09 | Nitto Boseki Co Ltd | 燃料電池用電極基板及びその製造方法 |
JPH03219566A (ja) * | 1990-01-25 | 1991-09-26 | Toho Rayon Co Ltd | 電池用電極材とその製法 |
JPH07254432A (ja) * | 1994-01-25 | 1995-10-03 | Toray Ind Inc | ナトリウム−硫黄電池用陽極集電体およびその製造方法 |
JP2000306587A (ja) * | 1999-04-21 | 2000-11-02 | Fujikoo:Kk | フェルト状導電材 |
WO2001004980A1 (en) * | 1999-07-07 | 2001-01-18 | Sgl Carbon Ag | Electrode substrate for electrochemical cells based on low-cost manufacturing processes |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
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JP3376711B2 (ja) * | 1994-09-20 | 2003-02-10 | 三菱化学株式会社 | 嵩密度の小さいアルミナ繊維ブランケットの製造法 |
JP4037943B2 (ja) * | 1997-11-25 | 2008-01-23 | 三菱レイヨン株式会社 | 炭素繊維フェルトの製造方法 |
-
2005
- 2005-10-14 KR KR1020077010030A patent/KR101209098B1/ko active IP Right Grant
- 2005-10-14 JP JP2006542943A patent/JP4531768B2/ja not_active Expired - Fee Related
- 2005-10-14 EP EP05793235.2A patent/EP1855346B1/en not_active Not-in-force
- 2005-10-14 US US11/666,897 patent/US7501109B2/en active Active
- 2005-10-14 WO PCT/JP2005/018948 patent/WO2006049005A1/ja active Application Filing
- 2005-10-14 CN CNB2005800368578A patent/CN100486028C/zh not_active Expired - Fee Related
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01253163A (ja) * | 1988-03-31 | 1989-10-09 | Nitto Boseki Co Ltd | 燃料電池用電極基板及びその製造方法 |
JPH03219566A (ja) * | 1990-01-25 | 1991-09-26 | Toho Rayon Co Ltd | 電池用電極材とその製法 |
JPH07254432A (ja) * | 1994-01-25 | 1995-10-03 | Toray Ind Inc | ナトリウム−硫黄電池用陽極集電体およびその製造方法 |
JP2000306587A (ja) * | 1999-04-21 | 2000-11-02 | Fujikoo:Kk | フェルト状導電材 |
WO2001004980A1 (en) * | 1999-07-07 | 2001-01-18 | Sgl Carbon Ag | Electrode substrate for electrochemical cells based on low-cost manufacturing processes |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20090011673A1 (en) * | 2007-07-03 | 2009-01-08 | Feng Chia University | Porous carbonized fabric with high efficiency and its preparation method and uses |
WO2009128215A1 (ja) * | 2008-04-14 | 2009-10-22 | 東洋炭素株式会社 | 炭素繊維炭素複合成形体及び炭素繊維強化炭素複合体材料並びにその製造方法 |
JP2009256117A (ja) * | 2008-04-14 | 2009-11-05 | Toyo Tanso Kk | 炭素繊維炭素複合成形体及び炭素繊維強化炭素複合体材料並びにその製造方法 |
CN102007090A (zh) * | 2008-04-14 | 2011-04-06 | 东洋炭素株式会社 | 碳纤维碳复合成型体、碳纤维强化碳复合体材料及其制造方法 |
JP2014167173A (ja) * | 2013-02-28 | 2014-09-11 | Toray Ind Inc | 炭素繊維不織布の製造方法および不織布 |
Also Published As
Publication number | Publication date |
---|---|
JP4531768B2 (ja) | 2010-08-25 |
EP1855346B1 (en) | 2017-12-06 |
CN100486028C (zh) | 2009-05-06 |
EP1855346A4 (en) | 2008-07-02 |
US20080131678A1 (en) | 2008-06-05 |
US7501109B2 (en) | 2009-03-10 |
EP1855346A1 (en) | 2007-11-14 |
KR20070083923A (ko) | 2007-08-24 |
KR101209098B1 (ko) | 2012-12-06 |
CN101048911A (zh) | 2007-10-03 |
JPWO2006049005A1 (ja) | 2008-05-29 |
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