Classifications

• • C—CHEMISTRY; METALLURGY
  • C01—INORGANIC CHEMISTRY
  • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
  • C01B32/00—Carbon; Compounds thereof
  • C01B32/30—Active carbon
  • C01B32/312—Preparation
  • C01B32/336—Preparation characterised by gaseous activating agents
• • H—ELECTRICITY
  • H01—ELECTRIC ELEMENTS
  • H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
  • H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
  • H01G11/22—Electrodes
  • H01G11/30—Electrodes characterised by their material
  • H01G11/32—Carbon-based
  • H01G11/34—Carbon-based characterised by carbonisation or activation of carbon
• • H—ELECTRICITY
  • H01—ELECTRIC ELEMENTS
  • H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
  • H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
  • H01G11/22—Electrodes
  • H01G11/30—Electrodes characterised by their material
  • H01G11/32—Carbon-based
  • H01G11/38—Carbon pastes or blends; Binders or additives therein
• • H—ELECTRICITY
  • H01—ELECTRIC ELEMENTS
  • H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
  • H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
  • H01G11/22—Electrodes
  • H01G11/30—Electrodes characterised by their material
  • H01G11/32—Carbon-based
  • H01G11/44—Raw materials therefor, e.g. resins or coal
• • H—ELECTRICITY
  • H01—ELECTRIC ELEMENTS
  • H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
  • H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
  • H01G11/84—Processes for the manufacture of hybrid or EDL capacitors, or components thereof
  • H01G11/86—Processes for the manufacture of hybrid or EDL capacitors, or components thereof specially adapted for electrodes
• • H—ELECTRICITY
  • H01—ELECTRIC ELEMENTS
  • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
  • H01M14/00—Electrochemical current or voltage generators not provided for in groups H01M6/00 - H01M12/00; Manufacture thereof
• • 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
  • H01M4/13—Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulators; Processes of manufacture thereof
  • H01M4/133—Electrodes based on carbonaceous material, e.g. graphite-intercalation compounds or CFx
• • 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
  • H01M4/36—Selection of substances as active materials, active masses, active liquids
  • H01M4/58—Selection of substances as active materials, active masses, active liquids of inorganic compounds other than oxides or hydroxides, e.g. sulfides, selenides, tellurides, halogenides or LiCoFy; of polyanionic structures, e.g. phosphates, silicates or borates
  • H01M4/583—Carbonaceous material, e.g. graphite-intercalation compounds or CFx
• • 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
  • H01M4/62—Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
  • H01M4/621—Binders
  • H01M4/622—Binders being polymers
• • 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
• • 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
• • 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
  • Y02E60/13—Energy storage using capacitors
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
  • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
  • Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
  • Y02E60/30—Hydrogen technology
  • Y02E60/50—Fuel cells

Definitions

• the present invention relates to a process for the preparation of activated carbon based on wood, preferably soft wood, and in particular pine wood, having a particular porous structure for the manufacture of electrodes for energy storage cells to electrochemical double layer.
• the invention also relates to the electrodes thus obtained as well as to the energy storage cells with a double electrochemical layer comprising such electrodes, as well as to a method of manufacturing these electrodes.
• the electrochemical energy storage can be carried out by means of three different devices each having their own characteristics.
• the two non-polarizable electrodes are separated by an ion conductor. Charge transfers are carried out by slow redox reactions. The maximum available power is therefore low ( ⁇ 400W / kg). On the other hand, the stored energy is important (> 30 WH / kg).
• the two polarizable electrodes are separated by a thin dielectric.
• the operating principle is based on the formation of an electric double layer by accumulation of charges within the electrodes on either side of the dielectric. This phenomenon is very rapid and allows charge-discharge periods of the order of a millisecond.
• the impulse power supplied by such systems is therefore extremely high (> 10 W / kg).
• the quantity of stored energy is low ( ⁇ 10 ⁇ 2 Wh / kg).
• the two polarizable electrodes with a large specific surface are separated by an ionic conductor.
• the supercapacitor is presented as an intermediate device between the accumulator and the capacitor.
• capacitors can be described in terms of energy density (kilowatt hour / kg) and power density (watts / kg) characteristics.
• High energy density capacitors store a relatively high capacitance which is discharged slowly over a period of a few minutes.
• capacitors with high power density can deliver their energy quickly (in a few milliseconds).
• Various practical applications have different requirements in terms of energy and power. Through for example, memory backup devices require a reasonably high energy density, but do not require energy to be delivered quickly (low power, long unloading time).
• an application such as starting an automobile engine requires very high power and most of the energy must be delivered in a few milliseconds.
• Other applications require combinations of the energy and power densities which are intermediate between these two extremes.
• Electric energy storage devices comprising electrodes based on activated carbon derived from lignocellulosic materials. These devices which are generally known as an electrochemical double-layer carbon capacitor, or CDLCs, usually consist of a pair of electrodes (at least one which is a carbon paste electrode), a separator, and a conductive collector of current impermeable to ions.
• CDLCs electrochemical double-layer carbon capacitor
• Activated charcoals are characterized by a large specific total surface (generally in the range 500-2500 m 2 / g). They are differentiated by their origin or precursor (coal, wood, fruit shells, etc.) as well as by the type of activation they have undergone, physical or chemical.
• the pores in activated carbon are classified according to their size in micropores (diameter ⁇ 2 nm), mesopores (diameter 2-50 nm) or macropores (diameter> 50 nm).
• CDLCs with high energy density obtained from activated charcoals having a particular porous structure consisting essentially of micropores are also known from US 5,926,361.
• CDLCs with high power density from activated carbon with an equivalent content of mesopores are also known from US 5,905,629.
• These coals are obtained by an activation process followed by a heat treatment of the activated carbon precursor.
• these CDLCs are not suitable for intermediate applications requiring both a high energy density and rapid energy delivery. The coal manufacturing process is also expensive.
• EP 1049116 discloses coals having a pore volume of 0.3 to 2.0 cm 3 / g, 10 to 60% of which are micropores, 20 to 70% of mesopores and not more than 20%) of macropores and with a specific surface of 1000 to 2500 m 2 / g.
• the coals described are exclusively obtained from polymers.
• the present invention therefore aims to provide a method of manufacturing activated charcoal having a porosity profile suitable for the electrodes of energy storage cells with double electrochemical layer.
• An object of the invention is therefore to propose a method for manufacturing a porous carbon material. Another object of the invention is to provide an electrode based on such materials and energy storage cells having a better compromise between the power density and the energy density compared to cells of this type already existing. Another object of the invention is a method of manufacturing such improved energy storage cells.
• energy storage cells means any electrochemical energy storage device, supercapacitors, and in particular CDLCs.
• the cells according to the invention are obtained using activated charcoals based on wood, preferably soft wood, and in particular pine wood which have a particular porous distribution and in particular have mesopore and micropore contents of less than 75%. of the total pore volume.
• This particular porous distribution is partly due to the quality of the raw material, the wood, preferably the soft wood, and in particular the pine wood.
• the coals obtained from pine wood, which are particularly preferred, are further characterized by high purity.
• the activated carbon has a mesopore content of less than 75%, preferably between 40 and 60%> relative to the total volume of the pores.
• the volume of mesopores of the activated carbon used is preferably between 0.4 and 0.8 cm 3 / g.
• these coals have a pore volume greater than 0.8 cm 3 / g, preferably greater than 1 cm 3 / g, a median pore width of 15 to 50 nm and a specific surface greater than 800 m 2 / g.
• activated carbons also preferably have (as a function of the total pore volume) a macropore content of less than 0.3 cm 3 / g.
• the relative content of macropores is preferably less than the content of micropores and mesopores.
• So activated charcoal advantageously comprises less than 25%, preferably less than 10% and even more preferably less than 1% of macropores relative to the total pore volume.
• coals are subjected to an activation process so as to increase the surface area of the natural carbonaceous material.
• activation process is carried out either by a chemical process or by a thermal process. Examples of the activation process are given, for example, in US Patents 4,107,084; 4,155,878; 5,212,144; and
• Effective porosity of activated carbon produced by thermal activation is the result of gasification of carbon at high temperature (after initial carbonization of the raw material), while the porosity of products activated by chemical dehydration / condensation reaction occur at low temperature.
• the activated carbon precursor used according to the invention is wood, preferably softwood, and in particular pine wood.
• the wood used may be, for example, in the form of wood chips, wood flour, wood dust, sawdust, and combinations thereof.
• Activated carbon can be obtained by chemical activation or preferably by thermal or physical activation.
• Chemical activation is generally carried out industrially in a simple oven.
• the precursor of the raw material is impregnated with a chemical activating agent, and the mixture is heated to a temperature of 450 ° C-700 ° C.
• Chemical activators reduce the formation of tar and other by-products, thereby increasing the yield.
• Suitable chemical activators include alkali metal hydroxides, carbonates, sulfides, and sulfates; alkaline earth carbonates, chlorides, and phosphates; phosphoric acid; polyphosphoric acid; zinc chloride; sulfuric acid; fuming sulfuric acid; and combinations thereof.
• Preferred among these agents are phosphoric acid and zinc chloride. The most preferred among all is phosphoric acid.
• the precursor is impregnated with the activating agent and then activated at around 550 ° C.
• the activated carbon is preferably obtained by thermal activation.
• the precursor material is subjected to a thermal carbonization treatment at a temperature between 500 and 800 ° C. in order to obtain charcoal which is subsequently activated at a temperature above 700 ° C., preferably between 800 and 1100 ° C, and even more preferably at a temperature between 950 and 1050 ° C.
• the thermal activation of charcoal takes place in a thin layer.
• thin is meant a layer with a thickness of approximately 2 to 5 cm.
• the activation is preferably carried out in an oven in which the precursor material circulates by gravity from top to bottom.
• the activation is carried out in the presence of water vapor and / or carbon dioxide.
• Activated carbons capable of being obtained according to the process described above are particularly preferred for the manufacture of electrodes of energy storage cells with a double electrochemical layer.
• a typical CDLC is composed of: (1) a pair of electrodes of which at least one (and preferably both) is a carbon paste electrode, (2) a porous ion-conducting separator, and (3) a collector impermeable to ions to ensure electrical contact with the electrodes and an electrolyte.
• the cell preferably has an energy density greater than 3 Wh / kg, in particular greater than 4 Wh / kg and an energy power greater than 4 kW / kg, in particular greater than 5 kW / kg.
• the new energy storage cells with a better compromise of power / energy densities are derived from activated carbon based on wood. These activated carbons are characterized in that they have a rate of micropores relative to the total volume of the pores of less than 75%, preferably between 20 and 40% relative to the total volume of the pores. Preferably, the volume of micropores of the activated carbon used is between 0.2 and 0.6 cm 3 / g.
• the method of manufacturing electrodes for CDLCs with high power and energy density comprises the application of an activated carbon derived from wood having a volume of mesopores and micropores as defined above on a support.
• the activated carbon is preferably ground to a size expressed in d 50 of approximately 30 micrometers and preferably in a dso of approximately 10 micrometers.
• the application is carried out by previously preparing a slip comprising activated carbon in powder form, a binder and a solvent.
• the slip is applied to the support and then the solvent is evaporated to form a film.
• the activated carbons are mixed with a binder, such as a polymeric binder, in an aqueous or organic solvent.
• a binder such as a polymeric binder
• polyethers such as polyoxyethylene (POE), polyoxypropylene (POP) and / or polyalcohols such as polyvinyl alcohol (PVA), ethylene-vinyl acetate copolymers (EVA).
• POE polyoxyethylene
• POP polyoxypropylene
• PVA polyalcohols
• PVA polyvinyl alcohol
• EVA ethylene-vinyl acetate copolymers
• the solvent can be any aqueous or organic solvent suitable for dissolving the binder used.
• solvent is for example acetonitrile for polymeric binders with POE, POP, PVA and / or EVA mud.
• the activated carbon is mixed with the polymer in a weight ratio of 10/90 to 60/40, preferably from 30/70 to 50/50. Then, the paste obtained is applied to a support by coating.
• the coating is advantageous for the coating to be carried out on a peelable support, for example using a template, generally of planar shape.
• the solvent is evaporated, for example in a hood.
• a film is obtained, the thickness of which depends in particular on the concentration of the coal paste and the deposition parameters, but which is generally between a few micrometers and a millimeter.
• the thickness is between 100 and 500 micrometers, and more preferably, it is between 150 and 250 micrometers.
• Suitable electrolytes to be used to produce high power and energy density CDLCs having at least one activated carbon based electrode having the capacity to deliver improved energy and power densities consist of any highly conductive medium.
• ions such as an aqueous solution of an acid, a salt or a base.
• non-aqueous electrolytes in which water is not used as a solvent
• Et NBF 4 tetraethylammonium tetrafluoroborate
• the electrolyte can have three general functions: as a promoter of the conductivity of ions, as a source of ions, and if necessary, as a binder for carbon particles. Sufficient electrolyte should be used to fulfill these functions (although a separate binder may be used to provide the binding function).
• the carbon paste comprises activated carbon, a binder and a solvent.
• One of the electrodes can be made of another material known in the art.
• the ion impermeable current collector (3) can be any electrically conductive material which is non-ionic conductive. Satisfactory materials to be used to produce these collectors include: coal, copper, lead, aluminum, gold, silver, iron, nickel, tantalum, conductive polymers, non-conductive polymers filled with conductive material to make the polymer electrically conductive, and the like.
• the collector (3) should be electrically connected to an electrode (1).
• a separator (2) Between the electrodes is a separator (2), generally made of a highly porous material, the functions of which are to provide electronic isolation between the electrodes (1) while letting the ions of the electrolyte pass.
• the separator pores (2) must be small enough to prevent electrode-electrode contact between the opposite electrodes (contact would result in a short circuit and rapid loss of the charges accumulated in the electrode).
• any conventional battery separator can be used in a CDLC with high power and energy density.
• the separator (2) can be an ion-permeable membrane that allows ions to pass through, but prevents electrons from passing through.
• the activated carbons of the following examples 2S to 5 S sold by the applicant are obtained industrially according to the method of claim 1 by adjusting the partial pressure of water vapor and increasing the residence time in the oven making it possible to go from quality 2S to 3S to 4S and to 5S by developing porosity more and more.
• Charcoals derived from thermally activated pine wood of 2S quality, available from CECA, are used to produce coal paste electrodes as described below. This activated carbon is obtained by activation in a thin layer at a temperature of 1000 ° C. in the presence of water vapor.
• a film is obtained whose dry thickness is approximately 200 micrometers.
• Charcoal paste electrodes are prepared in the same manner as described in Example 1 using activated charcoal derived from 3S quality pine wood, available from CECA. This activated carbon is activated in a thin layer at a temperature of 1000 ° C in the presence of water vapor.
• Charcoal paste electrodes are prepared in the same manner as described in Example 1 using activated charcoal derived from 4S quality pine wood, available from CECA. This activated carbon is obtained by activation at a temperature of 1000 ° C in the presence of water vapor.
• Charcoal paste electrodes are prepared in the same manner as described in Example 1 using activated charcoal derived from 5S quality pine wood, available from CECA. This activated carbon is obtained by activation at a temperature of 1000 ° C in the presence of water vapor.
• Charcoal paste electrodes are prepared in the same manner as described in Example 1 using the activated carbon OSAKA M15 (available from OSAKA GAS Co. Ltd.) and obtained from pitch mesophase.
• Charcoal paste electrodes are prepared in the same manner as described in Example 1 using activated charcoal of quality OSAKA M20 (available from OSAKA GAS Co. Ltd.) and obtained from pitch mesophase.
• Charcoal paste electrodes are prepared in the same manner as described in Example 1 using activated carbon of quality OSAKA M30 (available from OSAKA GAS Co. Ltd.) and obtained from pitch mesophase.
• Charcoal paste electrodes are prepared in the same manner as described in Example 1 using activated carbon of PUREF-LOW quality, available from (Norit Nederland) and obtained from mineral charcoal.
• Charcoal paste electrodes are prepared in the same manner as described in Example 1 using activated carbon of quality Norit SX +, available from (Norit Nederland) and obtained from peat.
• EXAMPLE 10 (comparison example)
• Charcoal paste electrodes are prepared in the same manner as described in Example 1 using activated carbon of quality Norit SX Ultra, available from (Norit Nederland) and obtained from peat.
• the active surface of the samples is determined by adsorption / desorption of nitrogen at 77 K.
• the electrodes prepared according to Examples 1 to 10 are then used to mount a measuring cell in order to evaluate their performance in a CDLC in terms of power and energy density.
• the electrode is first impregnated with a liquid organic electrolyte, a solution of tetraethyl ammonium tetrafluoroborate at 0.6M in ⁇ - butyrolactone for 1 h 30 min at atmospheric pressure.
• the impregnated electrodes are used to mount a capacitor as follows.
• a pair of electrodes is each placed on a treated aluminum plate and then assembled face to face, separated by a PUMA 50 / 0.30 separator paper (available from Bolloré).
• the two electrodes are connected to a potentiostat, one being connected first to a calibrated spring.
• a double electrochemical layer spontaneously forms at each of the electrode / electrolyte interfaces by accumulation of ionic species on the side of the electrolyte and of electric charges on the side. of the electrode, the amount of charge thus accumulated is proportional to the applied voltage and the surface capacity of the electrodes.
• Each double layer is characterized by its capacity. The overall system is therefore defined by 2 capacities in series and the total capacity is expressed by:
• the stored energy is directly proportional to the total capacity of the global system.
• the total resistance or the series resistance of a capacitor is the second major parameter that characterizes the system.
• the power of the CDLC is directly evaluated from its value.
• the power and energy density of the electrodes mounted in capacitors is evaluated by chronopotentiometry.
• the current density used is 1.5 mA cm and the limits of the intensiostatic cycling are 0 and 2.5 V. From the curve obtained, the series resistance and the capacitance of the capacitor are deduced.
• the series resistance is calculated from the measurement of the ohmic drop at the start of the discharge.
• the capacitance of the capacitor is determined from the slope of the discharge curve.
• the stored energy is directly proportional to this capacity in accordance with
• the 2 cm 2 electrodes are assembled in measuring cells to assess the energy and power density.
• the measurement results are presented in Table 3 below.
• the electrodes according to the invention have a balanced power and energy density, and that therefore this type of electrodes is suitable for CDLCs for intermediate applications requiring both a good density of energy and rapid energy delivery.
• coals that deliver improved power and energy density are useful for producing the carbon paste used in CDLCs, these coals can also be useful in other types of electrical devices in which activated carbon is used as electrode material (such as batteries, "fuel cells” or “fuel cells”, etc.).

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• Electric Double-Layer Capacitors Or The Like (AREA)
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