WO2004102717A1 - 液体燃料形燃料電池とその燃料 - Google Patents
液体燃料形燃料電池とその燃料 Download PDFInfo
- Publication number
- WO2004102717A1 WO2004102717A1 PCT/JP2004/004464 JP2004004464W WO2004102717A1 WO 2004102717 A1 WO2004102717 A1 WO 2004102717A1 JP 2004004464 W JP2004004464 W JP 2004004464W WO 2004102717 A1 WO2004102717 A1 WO 2004102717A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- fuel
- liquid
- electrode
- preservative
- liquid fuel
- Prior art date
Links
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M8/00—Fuel cells; Manufacture thereof
- H01M8/04—Auxiliary arrangements, e.g. for control of pressure or for circulation of fluids
- H01M8/04082—Arrangements for control of reactant parameters, e.g. pressure or concentration
- H01M8/04186—Arrangements for control of reactant parameters, e.g. pressure or concentration of liquid-charged or electrolyte-charged reactants
-
- 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
- H01M8/06—Combination of fuel cells with means for production of reactants or for treatment of residues
- H01M8/0662—Treatment of gaseous reactants or gaseous residues, e.g. cleaning
-
- 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
- H01M8/10—Fuel cells with solid electrolytes
- H01M8/1009—Fuel cells with solid electrolytes with one of the reactants being liquid, solid or liquid-charged
-
- 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 liquid fuel type fuel cell in which a fuel such as methanol, ethanol, isopropanol, ptanol, dimethinoleether is mixed with water and supplied directly to a fuel electrode, and a fuel used therefor.
- a fuel such as methanol, ethanol, isopropanol, ptanol, dimethinoleether is mixed with water and supplied directly to a fuel electrode, and a fuel used therefor.
- the present invention relates to prevention of accidental ingestion of fuel by a user and decay of fuel.
- Patent Document 1 JP 2001-313046 A
- Patent Document 1 proposes supplying fuel from a cartridge to a fuel tank.
- the fuel methanol is harmful if swallowed and is harmful to the skin.
- Methanol is colorless and transparent, and its odor is weak in an aqueous solution with a concentration of about 3 wt%, and there is a risk that a user of a fuel cell such as a general consumer may inadvertently treat methanol / water fuel in the same way as simple water.
- Fuels such as isopropanol / water / peptanol / water or dimethyl ether / water are still harmful to humans if swallowed.
- the inventor has found phenomena such as a portable direct methanol fuel cell that has been started to use once left undisturbed at room temperature for about one month, giving off-smelling odor, fuel that should be colorless and transparent, and discoloration of discharged fuel. .
- discolored fuel was observed, microorganisms such as molds and spoilage bacteria were detected, and the off-flavor was close to the formic acid odor, and was acidic and odorous.
- the inventor has experimentally confirmed that the output of the direct methanol fuel cell decreases due to the spoilage of the fuel and the like. This was corruption in direct methanol fuel cell in question, but by changing the fuel isopropanol / water and the like, since the complete oxidation of the fuel to the C 0 2 and water is more flame properly, nutrients for the microorganisms Corruption becomes a more serious problem.
- the propagation of microorganisms in the direct methanol fuel cell is a new problem that has not been studied so far. Summary of the Invention
- An object of the present invention is to prevent a user from accidentally ingesting fuel of a liquid fuel type fuel cell, or to prevent the fuel from being spoiled.
- An additional object of the present invention is to prevent the fuel cell from being adversely affected by coloring or smelling the fuel.
- An additional object of the present invention is to make it possible to easily remove additives and impurities in fuel / exhaust fuel, and to facilitate addition of additives to fuel / removal of impurities from exhaust fuel. It is in.
- An additional object of the present invention is to prevent performance deterioration of a fuel electrode and an air electrode due to a preservative. Structure and effect of the invention
- the liquid fuel fuel cell according to the present invention has an air electrode and a fuel electrode on both surfaces of the proton conductor membrane.
- an aqueous liquid fuel is supplied to the MEA fuel electrode, and air is supplied to the air electrode to generate electricity, so that the fuel is colored or smelled so that the user does not drink it accidentally.
- the fuel is characterized by adding a preservative to the fuel to prevent the fuel from spoiling.
- the liquid fuel type fuel cell according to the present invention is characterized in that a preservative is added to the battery to prevent the fuel from spoiling.
- the fuel for a liquid fuel type fuel cell is an aqueous liquid fuel for a liquid fuel type fuel cell using a proton conductor membrane, wherein the fuel is colored, smelled or added with a preservative. It is characterized by having.
- the fuel of the liquid fuel type fuel cell is colored or smelled, or the spreading agent is added, so that it is possible to prevent the user from accidentally swallowing or attaching to the skin due to coloring or smelling.
- the P-type antiseptic can prevent the occurrence of mold and spoilage bacteria.
- the fuel is colored black by dispersing the carbon fine powder in the fuel.
- Carbon is a material used in fuel cells as activated carbon for electrodes or as a carbon sheet outside the electrodes. Carbon itself is stable, and there is no risk of deteriorating cell performance due to poisoning of the electrodes.
- the fuel is colored by adding a dye to the fuel.
- the dye is preferably a dye capable of coloring the fuel with a small amount, and particularly preferably, a filter for removing the dye is provided upstream of the MEA to prevent contamination of the MEA by the dye.
- the material of the filter is preferably, for example, activated carbon. Since the filter has a service life, it is used, for example, as a filter cartridge which is removable from the fuel system.
- a carboxylic acid having 1 to 4 carbon atoms preferably, a carboxylic acid having 1 to 4 carbon atoms, or an ester of a carboxylic acid having 1 to 4 carbon atoms and an alcohol having 1 to 4 carbon atoms, or an alkyl group having 1 to 4 carbon atoms, Add ether to fuel to odor.
- odorants include battery reaction products or battery reaction products, such as formic acid and methyl formate in the case of methanol-water fuel, and butanoic acid and esters of butyric acid and butyl alcohol in the case of water fuel.
- carboxylic acid and fuel alcohol Liquid fuel fuel cells also operate on ether fuels such as dimethyl ether, and R-O-R'-type ethers (R and R 'are both alkyl groups with 4 to 4 carbon atoms) can be used as fuel. Or a compound similar to a compound used as a fuel.
- the most preferred odorants are formic acid and methyl formate, which are easily decomposed by the electrode reaction and do not poison the electrodes.
- the liquid fuel type fuel cell according to the present invention is also provided with an air electrode and a fuel electrode on both sides of a proton conductor membrane to form an MEA, supplying an aqueous liquid fuel to the MEA fuel electrode, and supplying air to the air electrode.
- a filter for removing additives or impurities in fuel or exhaust fuel is provided.
- the filter is a detachable filter cartridge.
- Preservatives may be added to the fuel, for example, or may be applied to the fuel tank, the walls of the exhaust fuel tank, at appropriate locations in these tanks, and the spacer around the MEA (composite conductive membrane and electrode). It is added to the wall and carbon sheet near MEA.
- adding a preservative to the fuel can preserve all positions from the fuel tank to the exhaust fuel tank, and a preservative is added every time fuel is added, which is convenient.
- the amount of preservative added is the concentration in the fuel, for example, lOwtppn! ⁇ Lwt ° /. And preferably lOOwtppm ⁇ : lwt%.
- Preservatives that do not poison the electrode catalyst of the fuel electrode or air electrode are preferable and are not particularly excluded, but glycerin, etc. undergoes incomplete decomposition at the electrode and the product poisons the electrode catalyst Possible and not preferred.
- oxygen-containing organic aromatic preservatives especially oxygen-containing organic aromatic preservatives in which the aromatic ring is not a heterocycle but a carbon ring, most preferably a benzene ring, are not easily decomposed by an electrode catalyst, Adsorption to the electrode catalyst and re-dissolution in the fuel are reversible, and there is little risk of poisoning the electrode catalyst, which is preferable.
- Such preservatives include, for example, paraoxybenzoic acid (H0- ⁇ -C00H) and its derivatives, paradihydroxybenzene (H0- ⁇ -0H) and its derivatives, and phenol and its derivatives.
- ⁇ represents a benzene ring, and the position of the active group is indicated by para, meta, ortho, etc.
- paraoxybenzoic acid or paradihydroxybenzene is indicated, but the positions of the two active groups are ortho, meta, etc. good.
- the kind of aromatic is not limited to benzene, but may be biphenyl-based naphthalene, azulene, anthracene or phenanthrene. Of these, Benzoic acid, dihydroxybenzene, phenol, and their derivatives are used in cosmetics and foods, and are safe to touch the skin when discarding fuel.
- silver compounds such as AgCl, copper compounds such as CU20, and compounds of Sn and Zn have an antiseptic effect. If a water-soluble inorganic compound is dissolved in a fuel, it may be reduced at the fuel electrode, for example, to form an alloy with the electrode catalyst. In contrast, when a water-insoluble inorganic preservative such as AgCl or CU20 is supported on a carrier such as activated carbon and added to the fuel, even if it adheres to the fuel electrode or air electrode, the activated carbon as the electrode material increases. No danger of poisoning.
- a silica gel preferably, the metal content is less than 100 ppm
- Preservatives those containing alkali metals or alkaline earth metals such as 300 wt PP m or more is not preferred, it may alter the conductivity of protons conductor film.
- an oxygen-containing organic aromatic preservative or an insoluble inorganic preservative supported on a carrier is used, there is little risk of poisoning the electrode catalyst or changing the conductivity of the proton conductor membrane, and discarding the exhaust fuel It is safe even if it comes in contact with the skin. Since the fuel used for the fuel cell is, for example, 90 wt% water, the inorganic preservative only needs to be insoluble in water.
- the type of fuel is preferably methanol-Z water, but ethanol water, isopropanol-Z water, butanol / water, dimethyl ether / water, etc., may be used, and the concentration may be determined appropriately according to a known technique.
- the materials and structures of the cell components such as the proton conductor membrane, the air electrode, and the fuel electrode are known, and may be determined appropriately.
- FIG. 1 is a block diagram of a direct methanol fuel cell according to an embodiment in which a coloring agent or an odorant is added.
- FIG. 2 is a sectional view of a main part of the filter cartridge used in the above embodiment.
- FIG. 3 is a perspective view of a direct methanol fuel cell according to another embodiment.
- FIG. 4 is an enlarged sectional view of a main part of the unit cell of FIG.
- FIG. 5 is a perspective view of a direct methanol fuel cell of an embodiment to which a preservative is added.
- FIG. 6 is a cross-sectional view of a main part corresponding to a unit cell of the direct methanol fuel cell of the above embodiment.
- FIG. 7 is a block diagram of a direct methanol fuel cell according to the above modification.
- FIG. 8 is a diagram showing initial characteristics of the direct methanol fuel cell of the above embodiment.
- FIG. 9 is a view showing characteristics of the direct methanol fuel cell of the above embodiment after being left at room temperature for one month.
- Example 1
- 1 to 4 show an embodiment using coloring and odor and its modification.
- 1 and 2 show an embodiment (embodiment 1) of a stationary direct methanol fuel cell 2.
- 4 is a cell stack
- 6 is a fuel tank
- 8 is a high-concentration methanol tank
- 10 is a drain tank.
- a fuel electrode and an air electrode are provided on both sides of a proton conductor membrane using a solid polymer, and MEA in which these are covered with, for example, a permeable carbon sheet is sandwiched between separators.
- the separator is, for example, a carbon plate or a stainless steel plate, and is provided with a fuel supply groove and an air supply groove to supply fuel and air.
- the fuel tank 6 contains an aqueous methanol solution of about 1 to 10 wt%, in this embodiment 3 wt%, and the high-concentration methanol tank 8 contains 10 to 60 wt%. /.
- the drain tank 10 stores the discharged fuel that has passed through the cell stack 4.
- 12-: 14 is a liquid sending pump, which controls these pumps while monitoring the methanol concentration in the fuel.
- the liquid sending pump 12 supplies a predetermined concentration of methanol aqueous solution from the fuel tank 6,
- the liquid sending pump 13 supplies methanol from the high-concentration methanol tank 8, and the liquid sending pump 14 is used for recirculating the waste fuel in the waste liquid tank 10.
- 16 is an air pump that supplies air to the air electrode side of the cell stack 4, and a filter cartridge 20 is attached to and detached from the fuel supply line 18 between the liquid feed pumps 12, 13 and the cell stack 4. Attach freely.
- FIG. 2 shows the structure of the filter cartridge 20.
- Reference numeral 22 denotes a pipe
- reference numeral 23 denotes a pair of front and rear lids
- reference numeral 24 denotes a ring for preventing fuel leakage, and the inside of the pipe 22.
- Reference numerals 28 and 28 denote glass filters, which can be changed to an appropriate filtering material to prevent activated carbon from spilling into the fuel supply line 18.
- Reference numeral 30 denotes a pipe for connecting the fuel supply line 18 to the filter cartridge 20. It is a removable joint.
- Activated carbon 26 removes dyes and the like used for coloring the fuel.
- the activated carbon may be in the form of granules or sheets, and a hollow fiber membrane or a silica gel filter may be used instead of the activated carbon.
- silica gel those having an alkali metal content of, for example, 100 ppm by weight or less are preferred.
- the filter cartridge 20 is preferably mounted, for example, at the fuel supply port to the cell stack 4 or between the pipes of the fuel supply line 18 as shown in FIG. It may be provided in the concentration methanol tank 8. For purposes other than the removal of the dye, it may be provided in the drainage tank 10.
- the dye in the fuel can be removed in the fuel tank 6 or the high-concentration methanol tank 8, or the impurities in the wastewater in the wastewater tank 10 can be removed to reuse the waste fuel.
- the filter cartridge 20 since the filter cartridge 20 has a finite life, when it is attached to the fuel supply line 18 etc., it is detachable via the joint 30 etc., and when it is installed in the tanks 6 to 10, it comes from the tank lid etc. It is preferable to be able to freely put in and out.
- a problem with the direct methanol fuel cell 2 is that a mixed solution of methanol and water in methanol is harmful. Therefore, in the embodiment, the methanol / water fuel is colored, for example.
- An appropriate dye or the like may be used for coloring, but a dye is preferably used.
- the dye may be an acidic dye, a basic dye, or another dye, but an acidic dye such as an azo dye is preferable to a basic dye or the like because of its high water solubility.
- the dyes for example, 0. 1 ⁇ : l00wt PP m, and preferably added in 0.. 5 to 20 wt PP m about fuel can color the fuel.
- the dye dissociates in the fuel into alkali metal ions, ammonium ions, and anions. Then, the alkali metal ions may ion-exchange with the protons in the proton conductor membrane to change the characteristics. In addition, the anion of the dye may adhere to the fuel electrode catalyst or the like and change the catalytic activity. Basic dyes do not contain alkali metal ions, but they may adhere to the fuel electrode catalyst and change their properties. Therefore, the dye is adsorbed and removed by the activated carbon 26 in the filter cartridge 20. Since the adsorption capacity of activated carbon is saturated when a large amount of dye is adsorbed, the filter cartridge 20 can be exchanged.
- An appropriate pigment or pigment may be added to color the fuel.
- carbon fine powder is preferably added as a pigment.
- Carbon materials such as activated carbon and carbon black are the main components of MEA electrode catalysts, and carbon is used in large amounts in carbon sheets used as gas diffusion layers. Therefore, even if the carbon fine powder adheres to the electrode or carbon sheet, the effect on the battery characteristics is small.
- the carbon fine powder include carbon black such as acetylene black, Ketjen black, and oil furnace black, and graphite fine powder and fullerene.Among these, it is easy to obtain a fine powder. Carbon black is preferable because it is hard and sedimented.
- the average particle size of the carbon fine powder preferably examples Eba 0.01 to 100 1 11 in the secondary particle size, Yori preferably from 0.3 to 30 111, most preferably 1 to: a 10 mu m.
- the hydrophilicity of the carbon fine powder can be appropriately adjusted depending on the type of fine powder, production conditions, and the like. If necessary, the hydrophilicity may be increased by treating with a small amount of a surfactant. It is preferable that the carbon fine powder is such that the carbon fine powder is uniformly dispersed in the fuel, or partially dispersed and partially floated on the fuel surface.
- the addition amount of the carbon fine powder is, for example, 0.03 to 10 wt%, preferably 0.03 to 3 wt%, and more preferably 0.1 to: Iwt with respect to the fuel. /. And
- an appropriate odor component may be added, but components originally contained in the fuel or generated by the electrode reaction from the fuel are preferable because they do not deteriorate the battery characteristics.
- a carboxylic acid having a number of carbon atoms of Sl to 4, particularly formic acid which is easily decomposed at the electrode is preferable.
- the ester of a carboxylic acid having 1 to 4 carbon atoms and an alcohol having 1 to 4 carbon atoms is an ester of a carboxylic acid generated by partial oxidation of the fuel and an alcohol of the fuel, thereby deteriorating the electrode characteristics. There is no fear of letting you do it.
- Such esters generally have a strong odor.
- Ethers (4) to (4) are substances that can themselves be used as fuel for liquid fuel type fuel cells. Therefore, if such ether is added to methanol Z water fuel, the user can be warned not to drink the fuel by the ether odor.
- the concentration of the odorant is preferably 1 to 20 wt%, more preferably 3 to: I0 wt%.
- the filter cartridge 20 When coloring with activated carbon or adding an odorant, the filter cartridge 20 is originally unnecessary. However, even in such a case, the filter These cartridges may be removed by providing a cartridge 20. Colorants and odorants are also provided to warn users when handling fuel to prevent accidental drinking or contact with skin. Therefore, the colorant and the odorant are components that need not be present once the fuel is filled in the fuel tank 6 or the high-concentration methanol tank 8. Example 2
- Figures 3 and 4 show a small direct methanol fuel cell 32 used for portable electronic equipment.
- Reference numeral 34 denotes a cell stack, in which a plurality of MEAs 35 are connected in series, 36 to 38 are separators, 40 is a fuel tank, 42 is a drainage tank, and 56 is an air supply hole.
- the valve 44 is for supplying colored or odorized fuel to the fuel tank 40 from a cartridge (not shown) or the like.
- the valve 45 discharges discharged fuel from the drain tank 42.
- Fig. 4 shows the configuration of a single cell.
- 46 is a proton conductor membrane, a solid polymer proton conductive membrane is used, 47 is a fuel electrode, 48 is an air electrode, 49, 5 0 is a breathable carbon sheet.
- the fuel electrode 47 uses activated carbon or the like carrying Pt-Ru, and the air electrode 48 uses activated carbon or the like carrying Pt.
- the carbon sheets 49 and 50 are air-permeable and conductive sheets.
- the fuel tank 40 contains methanol / water fuel 52, and supplies fuel to the fuel electrode 47 side by a capillary 54 such as a thread. Air is supplied to the air electrode 48 through an air supply hole 56, and the generated water is discharged through a capillary 55.
- the danger of using methanol as fuel is greater than that of the stationary fuel cell 2 because the user is a general consumer.
- the main purpose of coloring and smelling fuel is to warn when handling fuel cartridges or when fuel leaks. Therefore, in the case of the embodiments shown in FIGS. 3 and 4, the fuel is colored with fine carbon powder or dye, or is odorized with formic acid or methyl formate.
- the materials, particle diameters, concentrations, and the like of these coloring agents and odorants may be the same as those in the embodiment shown in FIGS.
- the carbon fine powder is used as the colorant, the carbon fine powder accumulates in the fuel tank 40 in the cartridge.
- a dye for example, an activated carbon sheet or an activated carbon granule formed in an appropriate shape is stored as a filter in the fuel tank 40, and the dye is removed in the fuel tank 40. Leave.
- the container of the fuel cartridge is made transparent, and the dye-added fuel is absorbed in the capillary or porous body and stored in the cartridge, so that the dye or capillary is dyed. Then, the fuel in the cartridge appears to be colored because the capillary and porous material are stained. However, since most of the dye is adsorbed on the capillary, etc., the fuel coming out of the cartridge into the fuel tank contains little dye, so the fuel cell does not need to remove the dye.
- an odorant most of the odorant is decomposed at the fuel electrode 47, and a part of the odorant crosses over the proton conductive membrane 46 and is discharged to the drainage tank 42. Test example
- Nafion 117 as a proton conductor film used
- Pt as fuel electrode - a Ru used after supported on active carbon
- c air electrode using PTFE and Nafion as a binder
- Pt supported on activated carbon was used, and the binder was also PTFE and Nafion.
- a proton conductor membrane was placed between the air electrode and the fuel electrode, carbon sheets were stacked above and below these, and the MEA was created by hot pressing.
- a graphite plate as a separator plate, forming an air supply passage and fuel supply passage with an air electrode side groove depth of 3 mm, a groove width of 3, a fuel electrode side groove depth of lmra, and a groove width of 3 mm did.
- the cell thus prepared was operated at a battery temperature of 80 ° C, and supplied at a flow rate of 4 ml / min using a 3% methanol aqueous solution to which a coloring agent or an odorant was added as a fuel.
- the air supply was 1 liter / min.
- the battery was operated continuously for 20 hours at an output current of 200 mA m 2 , and the maximum output density before and after the operation was measured.
- acetylene black having a secondary particle size of about 1 ⁇ m in which 0.01% by weight of 10% by weight was dispersed was used to evaluate the cell characteristics and the degree of coloring of the fuel.
- the results are shown in Table 1, where 0.03 wt. /.
- Fuel can be colored with the added calories, 10wt. /. Even with the addition of a certain amount, the change in battery characteristics was slight. Then 0.03 10wt carbon powder in fuel. /. When added to the extent, the color can warn the user, preferably 0.03 3 wt%, more preferably 0.1 lwt ° /. Added.
- Table 2 shows the results when formic acid, methyl formate, and a mixture of methyl formate and formic acid at a weight ratio of 11 were used as odorants. From this, it was found that these odorants did not affect the battery characteristics, and that they could be used as odorants.
- Table 3 shows the effect of battery characteristics when acid blue 9 was added to 100 wtppm of acid blue as a dye. In practical use, addition of about 5wtppm can sufficiently color, so the added calo of 100wtppm corresponds to an acceleration test at a 20-fold concentration. By changing the type of dye, it is possible to color well even at lower concentrations.
- the colorant and the odorant may be added in combination, or two types of colorants may be used in combination. It is desirable to add 1% or more of the odorant, and if 10% is added, the smell becomes sufficiently strong. Preferably, 3 to 1 ( ⁇ % is added. Effect of acetylene black
- Sample numbers with C are comparative examples, and sample numbers with E are examples.
- Fuel odor was evaluated by putting the fuel in a beaker and smelling it, and the number of subjects who felt discomfort among the 10 subjects.
- Fuel such as methanol-Z water to which a coloring agent and an odorant are added can be used in a liquid fuel type fuel cell by filling it into a cartridge or putting it in an appropriate container. In this case, it is only necessary to prevent misuse of the fuel before the fuel cell is used. The preference in this case, the type, concentration and average particle size of the colorant and odorant are the same as in the example. Further, a preservative may be added to fuel such as a cartridge. Finoletaka cartridge
- the filter cartridge 20 in FIG. 2 is not only used for removing dyes and the like in fuel, but also for removing various additives to fuel and various impurities in exhaust fuel. it can. Preferably, it is detachably attached to the fuel / exhaust fuel piping, the fuel-side inlet / exhaust-fuel-side outlet of the cell stack, or the fuel tank / high-concentration methanol tank or the exhaust fuel tank.
- Example 3
- test example 1 In the direct methanol fuel cell, the possibility of fuel spoilage and the effect of preservatives were confirmed by the following test examples. Test example
- Naf ion 117 was used for the electrolyte membrane (Naf ion is a registered trademark of DuPont).
- the fuel and air electrodes are made of commercially available Pt-Ru / C catalyst, Pt / C catalyst (Tanaka Kikinzoku) and Nafion solution (Aldrich), and PTFE solution (DuPont) to impart water repellency.
- the mixture was applied to carbon paper to produce a mixture. They were joined by hot pressing at 980 Nm 2 at 140 ° C. to obtain MEA (membrane electrode assembly).
- This MEA was sandwiched between graphite separator plates to form a unit cell having an effective electrode area of 36 cm 2 .
- the cell was heated to 90 ° C and operated for two weeks under the operating conditions of a fuel flow rate of 8 ml / min and an air flow rate of 5 l / min using four types of fuels A to D in Table 4, and then the current Z The initial values of the voltage characteristics were measured.
- the current-Z voltage characteristics were measured under the same conditions.
- Figure 8 shows the initial current-voltage characteristics. Samples B to D with preservatives and Sample A without preservatives had the same characteristics, and the effect of the preservatives was not observed in continuous operation for two weeks. This indicates that the electrode was not poisoned by the preservative. In addition, during continuous operation for two weeks, Sample A without preservatives showed the same performance as Samples B to D with preservatives, indicating that microorganisms are unlikely to grow under operating conditions at 90 ° C. Is shown.
- Figure 9 shows the characteristics of the above four types of cells after being left in the air for one month.
- sample A which had no preservatives, the battery characteristics were reduced by about 15%, and when power was generated, an odor was felt.
- sample B ⁇ with the preservative added calo! In), the battery characteristics did not decrease even after one month of storage, indicating that neither the poisoning of the electrode by the preservative nor the generation of microorganisms occurred.
- a fuel was prepared by adding activated carbon (silver chloride content: 2 wt%) on which silver chloride was deposited to 0.5 wt% of a 3 wt% methanol-Z water fuel.
- the preservative concentration in the fuel is lOOwtppm.
- FIGS. 5 and 6 show the direct methanol fuel cell 102 of the embodiment.
- the cell stack 104 is connected in series with the MEA 106 sandwiched between separators 107 to 109.
- Things. 110 is an air supply hole provided in the separators 107 and 109 to supply air to the air electrode.
- a fuel tank 1 12 and an exhaust fuel tank 1 14 are placed on the lower side of the cell stack 104, and methanol Z water fuel (concentration 1 to: about 0 wt%) is supplied from the pulp 115.
- the pulp is supplied and waste fuel is discarded from pulp.
- Fig. 6 shows the structure of a unit cell, where 120 is a proton conductor membrane such as Nafion 117, 121 is a fuel electrode such as Pt-Ru / C, and 122 is Pt / C etc.
- the air electrode The composition and structure of the fuel electrode 122 and the air electrode 122 are well known.
- Numerals 1 23 and 124 are carbon sheets, which are air permeable sheets between the fuel electrode 121 and the air electrode 122 and the separator 107.
- Reference numeral 125 denotes a capillary body which supplies methanol Z water fuel 128 from the fuel tank 112 to the carbon sheet 123 using, for example, a yarn.
- the capillary body 126 discharges generated water and the like from the carbon sheet 124 to the exhaust fuel tank 114.
- the operating temperature is around room temperature and the maximum is about 40 ° C, so that the rot may progress even during the operation of the fuel cell. Moreover, it is difficult to completely seal the air supply hole 110 when left unattended, and there is a risk that microorganisms may enter the pulp 115, 116 or the like. Therefore, parazoxybenzoic acid, paradihydroxybenzene, or pheno is added to methanol Z water fuel in fuel tank 112.
- a preservative such as a polyester, is added, for example, in an amount of about 0.01 to lwt%.
- Preservatives along with fuel and product water, are supplied to all parts, such as the MEA 106 and Emissions Tank 114, to prevent spoilage.
- the preservative does not react at the electrodes 1 2 1 and 1 2 2, but passes through the MEA 106 through the crossover and the gap around the MEA 106 and is discharged to the exhaust fuel tank 114 side And is discarded together with the generated water from valve 116.
- preservatives such as paraoxybenzoic acid, paradihydroxybenzene, or phenol are safe to touch when discarded.
- the location of the preservative is not limited to the fuel. For example, activated charcoal carrying water-insoluble inorganic preservatives, etc. in the form of powder or granulated or sheeted in the fuel tank 1 12 good.
- the organic aromatic preservative may be added to the fuel tank 112 and the exhaust fuel tank 114 by mixing with an appropriate extender to impart a delayed release property. Further, a preservative may be added to the surface of the carbon sheets 123, 124 on the side of the capillaries 125, 126, the capillaries 125, 126, and the like.
- FIG. 7 shows a direct methanol fuel cell 132 provided with a liquid sending pump 140 to 144.
- 13 4 is a cell stack, the operating temperature is about 60-80 ° C, 13 5 is a fuel tank, and 1 36 is 60 wt /.
- This is a methanol tank containing high-concentration methanol such as.
- 1 37 is an exhaust fuel tank that contains exhaust fuel and introduces C02 generated at the fuel electrode. Accordingly, when an organic aromatic preservative is used, a part of the preservative evaporates from the exhaust fuel tank 1337 and is lost.
- a radiator 138 liquefies the water vapor, cools it with air from the air pump 144, and circulates the drainage to the exhaust fuel tank 1337 via the liquid feed pump 14.3.
- 14 140 is a pump for supplying fuel from the fuel tank 13 5
- 14 1 is a pump for circulating the exhaust fuel from the exhaust fuel tank 13 7
- 14 2 is an addition of methanol from the methanol tank 13 36 Pump.
- An air pump 146 supplies air to the cell stack 136.
- the cell stack 134 is kept at a high temperature during operation, the possibility of corruption in this part is low.
- the exhaust fuel tank 13 7 and the radiator 13 8 may be rotten. Therefore, for example, the organic aromatic preservative or the like is added to the fuel in the fuel tank 135 to prevent decay. Since the added preservative is not lost except for evaporation from the exhaust fuel tank 1 37, etc.
- the concentration of the preservative in the fuel added to the fuel tank 135 is reduced to, for example, about 0.01 wt%, and the preservative lost due to evaporation from the exhaust fuel tank 137 is supplied.
- the direct methanol fuel cells shown in Figs. 5 and 6 when a preservative carrying activated carbon is added to the fuel, the activated carbon accumulates in the fuel tank 112.
- the direct methanol fuel cell 13 2 shown in FIG. 7 even if the preservative loaded with activated carbon is mixed with the fuel, it can be recycled with the waste fuel.
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Sustainable Development (AREA)
- Sustainable Energy (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Fuel Cell (AREA)
Abstract
Description
Claims
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/556,253 US20070042234A1 (en) | 2003-05-16 | 2004-03-29 | Liquid fuel type fuel cell and fuel therefor |
JP2005506150A JP4894261B2 (ja) | 2003-05-16 | 2004-03-29 | 液体燃料形燃料電池 |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2003139133 | 2003-05-16 | ||
JP2003-139135 | 2003-05-16 | ||
JP2003139135 | 2003-05-16 | ||
JP2003-139133 | 2003-05-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2004102717A1 true WO2004102717A1 (ja) | 2004-11-25 |
Family
ID=33455492
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2004/004464 WO2004102717A1 (ja) | 2003-05-16 | 2004-03-29 | 液体燃料形燃料電池とその燃料 |
Country Status (3)
Country | Link |
---|---|
US (1) | US20070042234A1 (ja) |
JP (1) | JP4894261B2 (ja) |
WO (1) | WO2004102717A1 (ja) |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2005040314A2 (en) * | 2003-10-17 | 2005-05-06 | The Gillette Company | Fuel composition in fuel cartridges for dmfcs |
JP2006261034A (ja) * | 2005-03-18 | 2006-09-28 | Toshiba Corp | 燃料電池用燃料 |
JP2006313701A (ja) * | 2005-05-09 | 2006-11-16 | Toshiba Corp | 燃料電池用液体燃料、燃料電池用燃料カートリッジ及び燃料電池 |
JP2006313702A (ja) * | 2005-05-09 | 2006-11-16 | Toshiba Corp | 燃料電池用燃料カートリッジ及び燃料電池 |
WO2006134975A1 (ja) | 2005-06-17 | 2006-12-21 | Kabushiki Kaisha Toshiba | 燃料電池用燃料、燃料電池用燃料カートリッジ及び燃料電池 |
JPWO2007145244A1 (ja) * | 2006-06-15 | 2009-11-05 | 株式会社東芝 | 燃料電池用燃料カートリッジ及び燃料電池 |
US7632321B2 (en) | 2001-11-01 | 2009-12-15 | Idatech, Llc | Fuel processing systems, fuel cell systems, and improved feedstocks therefor |
US7638214B2 (en) | 2005-05-25 | 2009-12-29 | The Gillette Company | Fuel cells |
US7923159B2 (en) * | 2005-10-19 | 2011-04-12 | Samsung Sdi Co., Ltd. | Water recovery system and direct liquid feed fuel cell having the same |
US8227129B2 (en) * | 2005-02-16 | 2012-07-24 | National Tsing Hua University | Passive micro fuel cell |
US8637207B2 (en) | 2005-05-09 | 2014-01-28 | Kabushiki Kaisha Toshiba | Liquid fuel, fuel cartridge and fuel cell |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2008091080A (ja) * | 2006-09-29 | 2008-04-17 | Casio Comput Co Ltd | 液体カートリッジ、発電装置及び電子機器 |
KR20090040124A (ko) * | 2007-10-19 | 2009-04-23 | 삼성에스디아이 주식회사 | 연료전지용 막-전극 어셈블리, 이의 제조방법, 및 이를포함하는 연료전지 시스템 |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001093551A (ja) * | 1999-09-21 | 2001-04-06 | Toshiba Corp | 燃料電池用液体燃料収容容器および燃料電池 |
JP2001093558A (ja) * | 1999-09-21 | 2001-04-06 | Toshiba Corp | 燃料電池用の燃料組成物 |
JP2001185188A (ja) * | 1999-12-24 | 2001-07-06 | Xcellsis Gmbh | 炭素および水素含有流体のためのタンク |
JP2003217634A (ja) * | 2002-01-11 | 2003-07-31 | Hewlett Packard Co <Hp> | 燃料電池のための染料ベース燃料表示器システム |
JP2003308871A (ja) * | 2002-04-15 | 2003-10-31 | Sharp Corp | 燃料電池の燃料供給用カートリッジおよびそのカートリッジを備えてなる燃料電池 |
JP2003331879A (ja) * | 2002-05-14 | 2003-11-21 | Seiko Epson Corp | 液体燃料カートリッジ及びこれを備えた燃料電池システム |
JP2004134355A (ja) * | 2002-08-16 | 2004-04-30 | Fuji Photo Film Co Ltd | 燃料電池、電子機器、携帯端末及びカメラ |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5599614A (en) * | 1995-03-15 | 1997-02-04 | W. L. Gore & Associates, Inc. | Integral composite membrane |
US5874476A (en) * | 1997-07-14 | 1999-02-23 | Rohm And Haas Company | Dihaloformaldoxime carbamates as antimicrobial agents |
JP4194843B2 (ja) * | 2001-02-05 | 2008-12-10 | 株式会社カネカ | プロトン伝導性高分子膜およびその製造方法 |
JP2004127620A (ja) * | 2002-09-30 | 2004-04-22 | Nissan Motor Co Ltd | 燃料電池冷却システム |
US7419060B2 (en) * | 2003-03-05 | 2008-09-02 | Hewlett-Packard Development Company, L.P. | Integrated fuel container and impurity removal cartridge |
CA2483824A1 (en) * | 2003-07-25 | 2005-01-25 | Albany International Techniweave, Inc. | Control of carbon coating microcrackings in fabrication of fuel cell gdl electrode layers(s) |
-
2004
- 2004-03-29 WO PCT/JP2004/004464 patent/WO2004102717A1/ja active Application Filing
- 2004-03-29 JP JP2005506150A patent/JP4894261B2/ja not_active Expired - Fee Related
- 2004-03-29 US US10/556,253 patent/US20070042234A1/en not_active Abandoned
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001093551A (ja) * | 1999-09-21 | 2001-04-06 | Toshiba Corp | 燃料電池用液体燃料収容容器および燃料電池 |
JP2001093558A (ja) * | 1999-09-21 | 2001-04-06 | Toshiba Corp | 燃料電池用の燃料組成物 |
JP2001185188A (ja) * | 1999-12-24 | 2001-07-06 | Xcellsis Gmbh | 炭素および水素含有流体のためのタンク |
JP2003217634A (ja) * | 2002-01-11 | 2003-07-31 | Hewlett Packard Co <Hp> | 燃料電池のための染料ベース燃料表示器システム |
JP2003308871A (ja) * | 2002-04-15 | 2003-10-31 | Sharp Corp | 燃料電池の燃料供給用カートリッジおよびそのカートリッジを備えてなる燃料電池 |
JP2003331879A (ja) * | 2002-05-14 | 2003-11-21 | Seiko Epson Corp | 液体燃料カートリッジ及びこれを備えた燃料電池システム |
JP2004134355A (ja) * | 2002-08-16 | 2004-04-30 | Fuji Photo Film Co Ltd | 燃料電池、電子機器、携帯端末及びカメラ |
Cited By (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7632321B2 (en) | 2001-11-01 | 2009-12-15 | Idatech, Llc | Fuel processing systems, fuel cell systems, and improved feedstocks therefor |
WO2005040314A3 (en) * | 2003-10-17 | 2005-07-21 | Gillette Co | Fuel composition in fuel cartridges for dmfcs |
WO2005040314A2 (en) * | 2003-10-17 | 2005-05-06 | The Gillette Company | Fuel composition in fuel cartridges for dmfcs |
US8227129B2 (en) * | 2005-02-16 | 2012-07-24 | National Tsing Hua University | Passive micro fuel cell |
JP2006261034A (ja) * | 2005-03-18 | 2006-09-28 | Toshiba Corp | 燃料電池用燃料 |
JP2006313701A (ja) * | 2005-05-09 | 2006-11-16 | Toshiba Corp | 燃料電池用液体燃料、燃料電池用燃料カートリッジ及び燃料電池 |
JP2006313702A (ja) * | 2005-05-09 | 2006-11-16 | Toshiba Corp | 燃料電池用燃料カートリッジ及び燃料電池 |
US8637207B2 (en) | 2005-05-09 | 2014-01-28 | Kabushiki Kaisha Toshiba | Liquid fuel, fuel cartridge and fuel cell |
US7767351B2 (en) | 2005-05-25 | 2010-08-03 | The Gillette Company | Fuel cell with cartridge and colorant |
US7638214B2 (en) | 2005-05-25 | 2009-12-29 | The Gillette Company | Fuel cells |
EP1901385A4 (en) * | 2005-06-17 | 2010-01-27 | Toshiba Kk | FUEL FOR FUEL CELL, FUEL CARTRIDGE FOR FUEL CELL AND FUEL CELL |
JPWO2006134975A1 (ja) * | 2005-06-17 | 2009-01-08 | 株式会社東芝 | 燃料電池用燃料、燃料電池用燃料カートリッジ及び燃料電池 |
US8197560B2 (en) | 2005-06-17 | 2012-06-12 | Kabushiki Kaisha Toshiba | Fuel for fuel cell, fuel cartridge for fuel cell and fuel cell |
EP1901385A1 (en) * | 2005-06-17 | 2008-03-19 | Kabushiki Kaisha Toshiba | Fuel for fuel cell, fuel cartridge for fuel cell and fuel cell |
WO2006134975A1 (ja) | 2005-06-17 | 2006-12-21 | Kabushiki Kaisha Toshiba | 燃料電池用燃料、燃料電池用燃料カートリッジ及び燃料電池 |
US7923159B2 (en) * | 2005-10-19 | 2011-04-12 | Samsung Sdi Co., Ltd. | Water recovery system and direct liquid feed fuel cell having the same |
JPWO2007145244A1 (ja) * | 2006-06-15 | 2009-11-05 | 株式会社東芝 | 燃料電池用燃料カートリッジ及び燃料電池 |
Also Published As
Publication number | Publication date |
---|---|
US20070042234A1 (en) | 2007-02-22 |
JPWO2004102717A1 (ja) | 2006-07-13 |
JP4894261B2 (ja) | 2012-03-14 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP4894261B2 (ja) | 液体燃料形燃料電池 | |
JP4202109B2 (ja) | 燃料電池システム | |
JP3883509B2 (ja) | 電気化学燃料電池用の液体燃料組成物 | |
Tran et al. | A fuel‐flexible alkaline direct liquid fuel cell | |
CN100448076C (zh) | 气体扩散电极和高分子电解质型燃料电池的制造方法以及气体扩散电极和高分子电解质型燃料电池 | |
US9083037B2 (en) | Fuel cell including cathode electrode using iron redox couple | |
JP4980197B2 (ja) | 燃料電池用電極、これを含む燃料電池用膜−電極接合体及びこれを含む燃料電池システム | |
KR20090021314A (ko) | Pem 연료 전지 막 전극 조립체 성분의 재생 방법 | |
WO2008033301A1 (en) | Fuel processing systems, fuel cell systems, and improved feedstocks therefor | |
JP2008159519A (ja) | 燃料電池 | |
WO2005088752A1 (ja) | 燃料電池システム | |
US20080280165A1 (en) | Fuel Cell Cathode and a Polymer Electrolyte Fuel Cell Having the Same | |
JP4333112B2 (ja) | 燃料電池システム | |
KR100668356B1 (ko) | 산소환원전극 및 이를 구비한 연료전지 | |
JP2005183014A (ja) | 直接型液体燃料電池発電装置及び直接型液体燃料電池用有害物質除去フィルター | |
CA2551607C (en) | Method for producing hydrogen and hydrogen producing apparatus used therefor | |
JP2013225433A (ja) | 燃料電池 | |
WO2007034756A1 (ja) | 燃料電池 | |
Cho et al. | Improved methanol tolerance using Pt/C in cathode of direct methanol fuel cell | |
CN100424922C (zh) | 液体燃料型燃料电池及其燃料 | |
JP2005327625A (ja) | 固体電解質型燃料電池 | |
Li et al. | Effective electrochemical sterilization based on electrocatalysis of oxygen reduction by multiwalled carbon nanotubes | |
WO2005095144A1 (ja) | 電気自動車 | |
JP5375623B2 (ja) | 固体高分子型燃料電池用触媒及びこれを用いた固体高分子型燃料電池用電極 | |
WO2007007915A1 (ja) | ハニカム型水素製造装置、それを用いた燃料電池発電装置、電気自動車、潜水船及び水素供給システム、並びに水素製造セル用反応管 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AK | Designated states |
Kind code of ref document: A1 Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BW BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE EG ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NA NI NO NZ OM PG PH PL PT RO RU SC SD SE SG SK SL SY TJ TM TN TR TT TZ UA UG US UZ VC VN YU ZA ZM ZW |
|
AL | Designated countries for regional patents |
Kind code of ref document: A1 Designated state(s): BW GH GM KE LS MW MZ SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IT LU MC NL PL PT RO SE SI SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
WWE | Wipo information: entry into national phase |
Ref document number: 20048121956 Country of ref document: CN |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2005506150 Country of ref document: JP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2007042234 Country of ref document: US Ref document number: 10556253 Country of ref document: US |
|
122 | Ep: pct application non-entry in european phase | ||
WWP | Wipo information: published in national office |
Ref document number: 10556253 Country of ref document: US |