WO2019240481A1 - 복합 중공사막, 이의 제조 방법, 이를 포함하는 중공사막 카트리지 및 연료 전지 막가습기 - Google Patents
복합 중공사막, 이의 제조 방법, 이를 포함하는 중공사막 카트리지 및 연료 전지 막가습기 Download PDFInfo
- Publication number
- WO2019240481A1 WO2019240481A1 PCT/KR2019/007039 KR2019007039W WO2019240481A1 WO 2019240481 A1 WO2019240481 A1 WO 2019240481A1 KR 2019007039 W KR2019007039 W KR 2019007039W WO 2019240481 A1 WO2019240481 A1 WO 2019240481A1
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- WO
- WIPO (PCT)
- Prior art keywords
- hollow fiber
- fiber membrane
- composite hollow
- composite
- membrane
- Prior art date
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- 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
- H01M8/1004—Fuel cells with solid electrolytes characterised by membrane-electrode assemblies [MEA]
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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
- H01M8/00—Fuel cells; Manufacture thereof
- H01M8/10—Fuel cells with solid electrolytes
- H01M8/1007—Fuel cells with solid electrolytes with both reactants being gaseous or vaporised
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
- B01D53/22—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by diffusion
- B01D2053/221—Devices
- B01D2053/223—Devices with hollow tubes
- B01D2053/224—Devices with hollow tubes with hollow fibres
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2313/00—Details relating to membrane modules or apparatus
- B01D2313/40—Adsorbents within the flow path
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2325/00—Details relating to properties of membranes
- B01D2325/02—Details relating to pores or porosity of the membranes
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2325/00—Details relating to properties of membranes
- B01D2325/02—Details relating to pores or porosity of the membranes
- B01D2325/0283—Pore size
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2325/00—Details relating to properties of membranes
- B01D2325/12—Adsorbents being present on the surface of the membranes or in the pores
-
- 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
- H01M2008/1095—Fuel cells with polymeric electrolytes
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/30—Hydrogen technology
- Y02E60/50—Fuel cells
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
- Y02P70/50—Manufacturing or production processes characterised by the final manufactured product
Definitions
- the present invention relates to a composite hollow fiber membrane, a method of manufacturing the same, a hollow fiber membrane cartridge and a fuel cell membrane humidifier including the same, more specifically, nitrogen oxides (NO x ), sulfur oxides (SO) in the humidification process without a separate gas filter device x ), a composite hollow fiber membrane capable of removing a gas such as ammonia (NH 3 ) to prevent the performance of the fuel cell, a method for producing the same, a hollow fiber membrane cartridge and a fuel cell membrane humidifier including the same.
- NO x nitrogen oxides
- SO sulfur oxides
- NH 3 ammonia
- a fuel cell is a power generation type battery which produces electricity by combining hydrogen and oxygen. Unlike general chemical cells such as batteries and accumulators, fuel cells can continue to produce electricity as long as hydrogen and oxygen are supplied, and have twice the efficiency of internal combustion engines due to no heat loss.
- the fuel cell is not only environmentally friendly but also has an advantage of reducing anxiety about resource depletion due to increased energy consumption.
- Such fuel cells are classified into polymer electrolyte fuel cells (PEMFCs), phosphoric acid fuel cells (PAFCs), molten carbonate fuel cells (MCFCs), and solid oxide fuel cells, depending on the type of electrolyte used. SOFC), alkaline fuel cell (AFC), and the like.
- PEMFCs polymer electrolyte fuel cells
- PAFCs phosphoric acid fuel cells
- MCFCs molten carbonate fuel cells
- SOFC sulfur oxide fuel cells
- AFC alkaline fuel cell
- Each of these fuel cells operates on essentially the same principle, but differs in the type of fuel used, operating temperature, catalyst, electrolyte, and the like.
- the polymer electrolyte fuel cell is known to be most promising not only in small stationary power generation equipment but also in transportation systems because it can operate at a lower temperature than other fuel cells and can be miniaturized due to its high power density.
- a polymer electrolyte membrane also called a proton exchange membrane
- MEA membrane-electrode assembly
- a method of humidifying a polymer electrolyte membrane includes 1) a bubbler humidification method in which water is supplied to a pressure vessel and a target gas is passed through a diffuser to supply moisture, and 2) a water content required for a fuel cell reaction is calculated. Direct injection to supply water directly to the gas stream pipe through the solenoid valve, and 3) membrane humidification to supply water to the gas fluid bed using a polymer membrane. Etc.
- a membrane humidification method of humidifying the polymer electrolyte membrane by providing water vapor to the gas supplied to the polymer electrolyte membrane using a membrane that selectively permeates only the water vapor contained in the exhaust gas is advantageous in that the humidifier can be reduced in weight and size.
- the selective permeable membrane used in the membrane humidification method is preferably a hollow fiber membrane having a large permeation area per unit volume when forming a module. That is, when the humidifier is manufactured using the hollow fiber membrane, the high density of the hollow fiber membrane with a large contact surface area is possible, so that the humidification of the fuel cell can be sufficiently performed even with a small capacity, the use of low-cost materials is possible, and the fuel cell is discharged at a high temperature. There is an advantage that can be reused through the humidifier to recover the moisture and heat contained in the offgas (offgas).
- the hot air supplied from the compressor and the blower in the fuel cell system flows into the stack through the humidifier, and nitrogen oxides (NO x ), sulfur oxides (SO x ), ammonia (NH 3 ), etc., contained in the air. If contaminants enter the stack of the fuel cell, the stack performance may be degraded. Therefore, a separate gas filter device is used which can remove these contaminants either before or after the air compressor / blower.
- NO x nitrogen oxides
- SO x sulfur oxides
- NH 3 ammonia
- An object of the present invention is to remove the contaminants such as nitrogen oxides (NO x ), sulfur oxides (SO x ), ammonia (NH 3 ) in the humidification process without a separate gas filter device to prevent performance degradation of the fuel cell It is to provide a composite hollow fiber membrane.
- Another object of the present invention is to provide a method for producing the composite hollow fiber membrane.
- Still another object of the present invention is to provide a hollow fiber membrane cartridge including the composite hollow fiber membrane.
- Still another object of the present invention is to provide a fuel cell membrane humidifier including the composite hollow fiber membrane.
- a contaminant which is coated on the hollow fiber membrane and the inner surface of the hollow fiber membrane to remove contaminants from air flowing along the lumen of the hollow fiber membrane It provides a composite hollow fiber membrane comprising a pollutant entrapping layer.
- the contaminants include nitrogen oxides, sulfur oxides, ammonia, or mixtures of two or more thereof.
- the contaminant collecting layer may include biochar, charcoal, active carbon, or a mixture of two or more thereof.
- the contaminant trapping layer may comprise poly (perfluorosulfonic acid) (PFSA), sulfonated polyethersulfone (S-PES), sulfonated polyarylethersulfone (S-PES) -PAES), sulfonated polystyrene (S-PS), sulfonated polyetherketone (S-PEK), and sulfonated polyetheretherketone (S-PEEK) It may include one or more acidic polymers selected from the group.
- PFSA poly (perfluorosulfonic acid)
- S-PES poly(perfluorosulfonic acid)
- S-PES sulfonated polyethersulfone
- S-PES sulfonated polyarylethersulfone
- S-PS sulfonated polystyrene
- S-PEK sulfonated polyetherketone
- S-PEEK sulfonated polyetherether
- the contaminant collecting layer may be present in the composite hollow fiber membrane in an amount of 1% by weight to 50% by weight based on the total weight of the composite hollow fiber membrane.
- the average pore size of the hollow fiber membrane is 0.1 nm to 100,000 nm, the average pore size of the composite hollow fiber membrane is 0.05 nm to 90,000 nm, the ratio of the average pore size of the composite hollow fiber membrane to the average pore size of the hollow fiber membrane May be greater than or equal to 50%.
- the porosity of the hollow fiber membrane may be 50% to 90%, the porosity of the composite hollow fiber membrane may be 45% to 85%, the ratio of the porosity of the composite hollow fiber membrane to the porosity of the hollow fiber membrane is 94.4% or more Can be.
- a coating mixture comprising a pollutant entrapping material (pollutant entrapping material) It provides a method for producing a composite hollow fiber membrane, comprising the step of coating on the inner surface of the hollow fiber membrane.
- the contaminants include nitrogen oxides, sulfur oxides, ammonia, or mixtures of two or more thereof.
- the coating mixture may be a solution in which the pollutant collecting material is dissolved in a solvent or a dispersion in which the pollutant collecting material is dispersed in a dispersion medium.
- the coating mixture may include 1 wt% to 30 wt% of the contaminant trapping material based on the total weight of the coating mixture.
- the coating step may include circulating the coating mixture through the hollow of the hollow fiber membrane.
- the method of manufacturing a composite hollow fiber membrane may include preparing a hollow fiber membrane bundle with a plurality of the hollow fiber membranes, and allowing a first fluid to flow along the hollows of the hollow fiber membranes and a second fluid to flow outside the hollow fiber membranes.
- the hollow fiber membrane bundle may further comprise the step of manufacturing a hollow fiber membrane module disposed therein, the coating step may be performed after the hollow fiber membrane module manufacturing.
- the viscosity of the coating mixture may be 50 to 10,000 cps, the coating mixture may be circulated at a flow rate of 0.1 to 30 LPM.
- the coating step may further include circulating dry air through the outside of the hollow fiber membranes after the circulation step of the coating mixture.
- the circulation step of the dry air may be performed by circulating dry air of 10 to 150 °C at a flow rate of 1 to 1,000 LPM.
- a plurality of composite hollow fiber membranes and a body portion in which the composite hollow fiber membranes are accommodated, each of the composite hollow fiber membranes, on the inner surface of the hollow fiber membrane, and the hollow fiber membrane Provided is a hollow fiber membrane cartridge, comprising a contaminant trapping layer coated to remove contaminants from air flowing along the hollow of the hollow fiber membrane.
- the contaminants include nitrogen oxides, sulfur oxides, ammonia, or mixtures of two or more thereof.
- the first fluid inlet through which the first fluid flows in, the first fluid outlet through which the first fluid flows out, the second fluid inlet through which the second fluid flows in, and the second fluid flows out A housing portion including a second fluid outlet being formed; And, a plurality of composite hollow fiber membranes for respectively performing moisture exchange between the first and second fluids, wherein the first fluid flows along the hollows of the composite hollow fiber membranes and the second fluid is external to the composite hollow fiber membranes.
- the composite hollow fiber membranes are installed inside the housing portion so as to flow, wherein one of the first and second fluids is low humidity air supplied from the outside and humidified through the water exchange,
- Each of the deserts includes a hollow fiber membrane; And a contaminant trapping layer coated on one of the outer surface and the inner surface of the hollow fiber membrane to remove the contaminants from the low humidity air by being in direct contact with the low humidity air.
- a fuel cell membrane humidifier comprising an oxide, sulfur oxide, ammonia or a mixture of two or more thereof.
- the pollutant collecting layer may include biotea, charcoal, activated carbon, or a mixture of two or more thereof.
- the first fluid flowing along the hollows of the composite hollow fiber membranes may be the low humidity air, and the pollutant collecting layer may be coated on an inner surface of the hollow fiber membranes.
- the composite hollow fiber membrane of the present invention can prevent deterioration of a fuel cell by removing gases such as nitrogen oxides (NO x ), sulfur oxides (SO x ), and ammonia (NH 3 ) during a humidification process without a separate gas filter device.
- gases such as nitrogen oxides (NO x ), sulfur oxides (SO x ), and ammonia (NH 3 ) during a humidification process without a separate gas filter device.
- FIG. 1 is a perspective view schematically showing a fuel cell membrane humidifier according to an embodiment of the present invention.
- FIGS 2 to 4 are perspective views schematically showing various modifications of the fuel cell membrane humidifier according to one embodiment of the present invention.
- FIG. 5 is a perspective view schematically showing a hollow fiber membrane cartridge according to an embodiment of the present invention.
- the composite hollow fiber membrane according to an embodiment of the present invention includes a hollow fiber membrane and a contaminant trapping layer coated on an inner surface of the hollow fiber membrane to remove contaminants from air flowing along the hollow of the hollow fiber membrane. do.
- the contaminants to be removed by the contaminant collection layer may include nitrogen oxides (NO x ), sulfur oxides (SO x ), ammonia (NH 3 ), or a mixture of two or more thereof.
- the term 'hollow fiber membrane' refers to a normal hollow fiber membrane which is one component of the composite hollow fiber membrane, unless explicitly stated as a 'composite hollow fiber membrane'. It may be a 'single-layered hollow fiber membrane' or 'braid-reinforced hollow fiber membrane'.
- the material of the hollow fiber membrane (the material of the polymer film coated on the outer surface of the tubular braid in the case of a braid-reinforced hollow fiber membrane) can be used as long as it can selectively transmit moisture.
- the hollow fiber membrane may be polysulfone, polyethersulfone, polyarylene sulfone, polyarylene ether sulfone, polyimide, polyetherimide, polyamideimide, polyvinyl alcohol, polyacrylonitrile, polyvinylidene di Fluoride (PVDF), tetrafluoroethylene-perfluoro-dioxa-methyl-octysulfonic acid copolymer, copolymers thereof, or mixtures thereof.
- PVDF polyvinylidene di Fluoride
- the inner surface of the hollow fiber membrane coated with the pollutant collecting layer means a surface facing the hollow of the hollow fiber membrane.
- the pollutant trapping layer the pollutant such as nitrogen oxides (NO x ), sulfur oxides (SO x ), and ammonia (NH 3 ) may be collected in a humidification process without a separate gas filter device.
- the performance degradation of the fuel cell can be prevented. That is, in a fuel cell system, hot air supplied from a compressor and a blower flows into a stack through a humidifier. Nitric oxide (NO), nitrogen dioxide (NO 2 ), and dinitrogen monoxide contained in the air are included in the stack.
- Nitrogen oxides (Dinitrogen monoxide, N 2 O), dinitrogen trioxide (N 2 O 3 ), dinitrogen tetraoxide (Dinitrogen tetroxide, N 2 O 4 ), dinitrogen pentoxide (Dinitrogen pentoxide, N 2 O 5 ) NO x) and sulfur dioxide (SO 2), sulfur trioxide (SO 3), sulfurous acid (H 2 SO 3), sulfuric acid (H 2 SO 4) sulfur oxides, such as (SO x), and ammonia (NH 3) contamination, such as Material entering the stack of fuel cells can degrade the stack's performance.
- the air is humidified by collecting the pollutants by the pollutant collecting layer included in the composite hollow fiber membrane (ie, removing the substances from the air before air is introduced into the stack). The performance degradation of a battery can be prevented.
- the pollutant collecting layer may include biochar, charcoal, active carbon, or a mixture of two or more thereof as a pollutant collecting material.
- the particle size of the pollutant trapping material may be 0.1 ⁇ m to 50 ⁇ m, specifically 0.1 ⁇ m to 5 ⁇ m.
- the pollutant trapping material may be lost due to flow or the pollutant collecting efficiency of the pollutant collecting layer may be reduced.
- the contaminant trapping layer may comprise poly (perfluorosulfonic acid) (PFSA), sulfonated polyethersulfone (S-PES), sulfonated polyarylethersulfone (S-PES) -PAES), sulfonated polystyrene (S-PS), sulfonated polyetherketone (S-PEK), and sulfonated polyetheretherketone (S-PEEK) It may include one or more acidic polymers selected from the group.
- PFSA poly (perfluorosulfonic acid)
- S-PES poly(perfluorosulfonic acid)
- S-PES sulfonated polyethersulfone
- S-PES sulfonated polyarylethersulfone
- S-PS sulfonated polystyrene
- S-PEK sulfonated polyetherketone
- S-PEEK sulfonated polyetherether
- the thickness of the contaminant collecting layer may be 0.1 ⁇ m to 30 ⁇ m, and specifically 1 ⁇ m to 10 ⁇ m.
- the thickness of the pollutant collecting layer is less than 0.1 ⁇ m, the pollutant collecting efficiency may be reduced, and when the thickness of the pollutant collecting layer is greater than 30 ⁇ m, the humidification performance may be reduced.
- the contaminant trapping layer may be present in the composite hollow fiber membrane in an amount of 1 wt% to 50 wt%, specifically 5 wt% to 20 wt%, based on the total weight of the composite hollow fiber membrane.
- the pollutant collecting efficiency may decrease, and when the content of the pollutant collecting layer exceeds 50% by weight, the mechanical properties of the composite hollow fiber membrane may decrease.
- the composite hollow fiber membrane may be prepared by circulating a coating mixture including the pollutant trapping material through the hollow of the hollow fiber membrane.
- the pollutant trapping layer may be formed by flowing dry air to the outside of the hollow fiber membrane to cause moisture exchange. That is, by forming the pollutant collecting layer while the water exchange occurs, it is possible to prevent the pores of the hollow fiber membrane is blocked by the pollutant collecting layer or the porosity is changed. Therefore, according to one embodiment of the present invention, the pollutant may be efficiently collected by the pollutant collecting layer of the composite hollow fiber membrane without deteriorating the humidification efficiency.
- the average pore size of the hollow fiber membrane may be 0.1 nm to 100,000 nm, specifically 0.4 nm to 30,000 nm, the porosity of the hollow fiber membrane may be 50% to 90%, specifically 65% to 85%. . If the average pore size of the hollow fiber membrane is less than 0.1 nm, the humidification performance may be lowered, and if it exceeds 100,000 nm, the physical strength of the composite hollow fiber membrane may be lowered. In addition, when the porosity of the hollow fiber membrane is less than 50%, the humidification performance may be lowered, and when it exceeds 90%, the physical strength of the composite hollow fiber membrane may be lowered.
- the average pore size of the composite hollow fiber membrane may be 0.05 nm to 90,000 nm, specifically 0.4 nm to 30,000 nm, the porosity of the composite hollow fiber membrane may be 45% to 85%, specifically 63% to 83%. have.
- the average pore size of the composite hollow fiber membrane is less than 0.05 nm, the humidification performance may be lowered, and when the average hollow pore size exceeds 90,000 nm, the physical strength of the composite hollow fiber membrane may be reduced.
- the porosity of the composite hollow fiber membrane is less than 45%, the humidification performance may be lowered, and when it exceeds 85%, the physical strength of the composite hollow fiber membrane may be lowered.
- the rate of change of the average pore size according to the coating of the contaminant collecting layer may be 50% or less, specifically 10% to 50% (that is, the average pore size of the composite hollow fiber membrane with respect to the average pore size of the hollow fiber membrane). May be at least 50%, specifically 50% to 90%).
- the rate of change of porosity according to the coating of the contaminant collecting layer may be 5.6% or less, specifically 1% to 3% (ie, the ratio of porosity of the composite hollow fiber membrane to the porosity of the hollow fiber membrane is 94.4% or more, specifically, 94.4% to 97%).
- the average pore size change rate and the porosity change rate may be calculated by Equation 1 and Equation 2, respectively.
- % Of average pore size change [(average pore size of hollow fiber membrane-average pore size of composite hollow fiber membrane) / average pore size of hollow fiber membrane] X 100
- the humidification performance may decrease, and the hollow fiber membrane If the ratio of the porosity of the composite hollow fiber membrane to the average porosity of is less than 94.4% (that is, if the porosity change rate exceeds 5.6%), the humidification performance may decrease.
- a method of manufacturing a hollow fiber membrane includes preparing a hollow fiber membrane, and coating a coating mixture including a contaminant trapping material on an inner surface of the hollow fiber membrane.
- composition for hollow fiber membrane formation containing the polymer for hollow fiber membrane formation and a solvent is manufactured.
- the polymer for forming the hollow fiber membrane is the same as that described in the section related to the material of the hollow fiber membrane, repeated description thereof will be omitted.
- the solvent is N, N-dimethyl acetamide (DMAc), N, N-dimethyl formamide (DMF), N-methyl-2-pyrrolidone (NMP) ), Dimethyl sulfoxide (DMSO), methyl ethyl ketone (MEK), gamma butyrolactone ( ⁇ -butyrolactone), sulfolane, or 1,3-dimethyl-2-imidazoli Dinon and the like can be exemplified, but the present invention is not limited thereto.
- DMAc N, N-dimethyl formamide
- NMP N-methyl-2-pyrrolidone
- DMSO Dimethyl sulfoxide
- MEK methyl ethyl ketone
- ⁇ -butyrolactone gamma butyrolactone
- sulfolane 1,3-dimethyl-2-imidazoli Dinon and the like
- the hollow fiber membrane-forming polymer may be included in 10% by weight to 50% by weight relative to the total weight of the hollow fiber membrane-forming composition, specifically, may be included in 13% by weight to 38% by weight.
- the content of the hollow fiber membrane-forming polymer is less than 10% by weight, the manufacturing stability may be lowered, and when it exceeds 50% by weight, the humidification performance may be lowered.
- the hollow fiber membrane-forming composition may further include an additive.
- the additive may be any one selected from the group consisting of sorbitol, polyethylene glycol, ethylene glycol, polypropylene glycol, propylene glycol, diethylene glycol, glycerin, lithium chloride, lithium bromide, water, and mixtures thereof.
- the hollow fiber membrane-forming composition was spun and the immersed in an external coagulation liquid to prepare the hollow fiber membrane.
- the internal coagulating solution may be spun together.
- the spinning nozzle may be a single tubular nozzle or a multi-tubular spinning nozzle.
- the composition for forming the hollow fiber membrane may be injected into the outer tube, and the internal coagulating solution may be injected into the inner tube to spin the same.
- the spinning nozzle is preferably maintained at 50 °C to 150 °C, if the temperature is less than 50 °C the viscosity of the spinning stock solution is greatly increased, the spinning may not be smooth, if it exceeds 150 °C single yarn is difficult to continuous spinning Can be.
- the internal coagulating solution serves to form the hollow of the hollow fiber membrane, water, polyvinylpyrrolidone, N, N-dimethyl acetamide (dimethyl acetamide, DMAc), N, N-dimethyl formamide (dimethyl formamide, DMF), N-methyl-2-pyrrolidone (NMP), dimethyl sulfoxide (DMSO), methyl ethyl ketone (MEK), gamma butyrolactone ( ⁇ -butyrolactone) , Any one solvent selected from the group consisting of sulfolane, 1,3-dimethyl-2-imidazolidinone and mixtures thereof, sorbitol, polyethylene glycol, ethylene glycol, polypropylene glycol, It may be a mixed solution in which an additive selected from the group consisting of propylene glycol, diethylene glycol, glycerin, lithium chloride, lithium bromide, water, and mixtures thereof is mixed.
- the internal coagulating solution may be a mixture weight ratio of the solvent and the additive is 70:30 to 40:60.
- the weight ratio of the additive is less than 30, the macropores in the form of fingers can be formed in the entire hollow fiber membrane, when the weight ratio of the additive exceeds 60, the hollow fiber membrane having a structure of the interior blocked due to the slow phase transition speed have.
- the hollow fiber membrane-forming composition and the internal coagulant may be discharged through the spinning nozzle, respectively, and then the hollow fiber membrane may be formed by immersion in an external coagulation solution to solidify.
- the external coagulant is not particularly limited in the present invention, for example, water, dibutyl phthalate, dimethyl phthalate, diethyl phthalate, dioctyl phthalate, Any one selected from the group consisting of dioctyl sebacate, glycerol triacetate, polyethylene glycol, ethylene glycol, propylene glycol, diethylene glycol, isopropyl alcohol, methanol, ethanol and mixtures thereof Can be.
- the temperature of the coagulation bath including the external coagulation solution may be maintained at 10 ° C to 110 ° C, specifically 60 ° C to 100 ° C to solidify the spun hollow fiber membrane. If the temperature of the coagulation bath is less than 10 °C the temperature of the composition for forming the hollow fiber film may be drastically reduced, it may be difficult to implement the desired structure, if the temperature exceeds 110 °C solidification of the composition for forming the hollow fiber membrane is slow to proceed May occur.
- the manufactured hollow fiber membrane may further include the step of feeding continuously by stretching in a stretching machine including a stretching solution.
- the stretching solution may be any one selected from the group consisting of ethylene glycol, glycerol, polyethylene glycol having a molecular weight of 400 g / mol or less, water, and mixtures thereof.
- the stretching may be performed at a stretching ratio of 1.1 times to 2.0 times at a stretching temperature of 15 ° C to 150 ° C.
- a stretching temperature 15 ° C to 150 ° C.
- the stretching temperature is less than 15 °C partial stretching occurs the hollow fiber membrane may not be uniformly stretched, if it exceeds 150 °C may cause membrane shrinkage and cutting.
- the draw ratio is less than 1.1 times the length of the hollow fiber membrane, the effects of the process control and the strength increase due to the draw is insufficient, and when the draw ratio exceeds 2.0 times, the film thickness may be reduced to weaken the mechanical properties.
- a coating mixture comprising the contaminant trapping material is coated on the inner surface of the hollow fiber membrane.
- a coating mixture comprising the contaminant trapping material is prepared.
- the coating mixture may be a solution in which the pollutant collecting material is dissolved in a solvent or a dispersion in which the pollutant collecting material is dispersed in a dispersion medium.
- the solvent or dispersion medium may be any one selected from the group consisting of isopropyl alcohol, isobutanol, hexanol, N-methylpyrrolidone, dimethylacetamide, dimethyl sulfoxide, dimethylformamide and mixtures thereof.
- the coating mixture may further comprise an additive.
- the additive controls the pore structure and the porosity of the pollutant collecting layer, thereby preventing the pores of the hollow fiber membrane from being blocked by the pollutant collecting layer or changing the porosity, thereby reducing the pollutants without deteriorating the humidification efficiency. Allow for efficient collection.
- the additive may be any one selected from the group consisting of methoxyethanol, butoxyethanol, tetrahydrofuran, and pentanol.
- the additive may control the pore size of the contaminant collecting layer by controlling the rate of water exchange of the solvent / dispersion medium.
- the coating mixture may comprise 70% to 99% by weight of the solvent, 1% to 30% by weight of the contaminant trapping material, and, optionally, the remainder of the additive based on the total weight thereof.
- the coating may not be performed.
- the coating thickness becomes thick, so that the humidification performance is lowered and the required inter-membrane pressure (TMP) is required. This can be increased.
- the coating step may include circulating the coating mixture through the hollow of the hollow fiber membrane.
- the pollutant trapping layer may be coated while flowing dry air to the outside of the hollow fiber membrane in which the coating mixture does not flow, thereby causing moisture exchange, whereby pores of the hollow fiber membrane are blocked by the pollutant trapping layer.
- the coating step may be performed after the hollow fiber membrane module is manufactured.
- the hollow fiber membrane bundle is prepared with a plurality of the hollow fiber membranes, and the hollow fiber membrane bundle is disposed therein so that a first fluid flows along the hollows of the hollow fiber membranes and a second fluid flows outside the hollow fiber membranes.
- Prepared hollow fiber membrane module, and then the coating mixture can be circulated through the hollows of the hollow fiber membranes.
- the dry air may be circulated to the outside of the hollow fiber membranes.
- the viscosity of the coating mixture may be 50 cps to 10,000 cps.
- the coating mixture may be circulated at a flow rate of 0.1 LPM to 30 LPM, specifically 1 LPM to 10 LPM. If the viscosity of the coating mixture is less than 50 cps, or if the circulation rate is less than 0.1 LPM, the thickness of the contaminant trapping layer may be too thick, the viscosity of the coating mixture is greater than 10,000 cps, or the circulation rate is greater than 30 LPM. In this case, the coating may not be performed.
- the step of circulating the dry air may be carried out by circulating the dry air of 10 °C to 100 °C, specifically 30 °C to 70 °C at a flow rate of 1 LPM to 1,000 LPM, specifically 50 LPM to 300 LPM. If the temperature of the dry air is less than 10 ° C it may be difficult to control the temperature, if it exceeds 100 ° C may cause the contaminant trap layer due to rapid drying. If the flow rate of the dry air is less than 0.1 LPM, the drying rate is low, the coating may be made non-uniform, and if it exceeds 1,000 LPM, the coating may not be made due to the loss of the coating mixture.
- the hollow fiber membrane cartridge according to another embodiment of the present invention includes a plurality of the composite hollow fiber membranes and a body portion in which the composite hollow fiber membranes are accommodated.
- Each of the composite hollow fiber membranes includes a hollow fiber membrane and a contaminant trapping layer coated on an inner surface of the hollow fiber membrane to remove contaminants from air flowing along the hollow of the hollow fiber membrane.
- the fuel cell membrane humidifier according to another embodiment of the present invention includes the hollow fiber membrane cartridge.
- FIG. 1 is a perspective view schematically showing the fuel cell membrane humidifier
- FIGS. 2 to 4 are perspective views schematically showing various modifications of the fuel cell membrane humidifier
- FIG. 5 is a schematic view of the hollow fiber membrane cartridge. A perspective view is shown.
- the hollow fiber membrane cartridge and the fuel cell membrane humidifier will be described with reference to FIGS. 1 to 5.
- the fuel cell membrane humidifier may include a housing part 100 and a hollow fiber membrane cartridge 200.
- the housing part 100 forms an outer shape of the membrane humidifier.
- the housing part 100 may include the housing body 110 and the housing caps 120, and may be a unitary body in which they are coupled.
- the housing body 110 and the housing cap 120 may be made of a hard plastic or metal such as polycarbonate.
- the housing body 110 and the housing cap 120 may have a cross section in the form of a single closed curve.
- the cross section may be circular, or as shown in FIGS. 2 and 4, the cross section may be polygonal.
- the polygon may be a quadrangle, a square, a trapezoid, a parallelogram, a pentagon, a hexagon, or the like, and the polygon may have a rounded corner.
- the circle may be elliptical.
- the housing body 110 is formed with a second fluid inlet 131 through which a second fluid is supplied and a second fluid outlet 132 through which the second fluid is discharged.
- the housing cap 120 is coupled to each end of the housing body 110.
- One housing cap 120 has a first fluid inlet 121
- the other housing cap 120 has a first fluid outlet 122.
- the first fluid introduced into the first fluid inlet 121 of one housing cap 120 passes through the hollow of the composite hollow fiber membrane F of the present invention, and then the first fluid of the other housing cap 120 is Discharged through the outlet 122.
- the first fluid may be a low humidity fluid and the second fluid may be a high humidity fluid.
- the second fluid may be a low humidity fluid and the first fluid may be a high humidity fluid.
- Each of the composite hollow fiber membranes F is coated on one of the hollow fiber membrane and the outer surface and the inner surface of the hollow fiber membrane to flow the low humidity air to directly contact the low humidity air to remove contaminants from the low humidity air. Contain a contaminant trapping layer.
- the fuel cell membrane humidifier may include one hollow fiber membrane cartridge 200, and as illustrated in FIGS. 3 and 4, a plurality of hollow fiber membrane cartridges. 200 may be included.
- each of the hollow fiber membrane cartridges 200 may include a bundle of composite hollow fiber membranes F and a body part 211 surrounding the bundle.
- the fuel cell membrane humidifier may include the composite hollow fiber membrane F bundle directly inside the housing part 100 without the body part 211, wherein the hollow The desert (F) bundle may be partitioned into a plurality of sub-bundles by partition walls installed in the housing part 100.
- the body part 211 forms an outer shape of the hollow fiber membrane cartridge 200, and a structure for being installed inside the housing part 100 may be formed on an outer circumferential surface of the body part 211.
- the body part 211 may include a first mesh part 213 and the hollow fiber membrane cartridge 200 to allow the second fluid introduced into the second fluid inlet 131 to be introduced into the body part 211.
- the body portion 211 may also have a cross-section in the form of a single closed curve (eg, circular or polygonal). May be rounded. In addition, the circle may be elliptical. Meanwhile, potting portions (not shown) may be formed at both ends of the hollow fiber membrane cartridge 200 to fill the voids between the composite hollow fiber membranes F while binding the bundle of the composite hollow fiber membranes F. That is, one end of the composite hollow fiber membranes F may be potted in the potting part.
- the hollow fiber membrane cartridge 200 is formed by separating the flow path through the hollows of the composite hollow fiber membranes F and the flow path through the outside of the composite hollow fiber membranes F from each other.
- the material of the potting part may be a known material such as polyurethane, but is not limited thereto.
- the first fluid is a low humidity fluid
- the second fluid is a high humidity fluid
- the pollutant trapping layer of each of the composite hollow fiber membranes F is described as being coated on the inner surface of the hollow fiber membrane.
- the present invention is not limited thereto, and the second fluid is a low humidity fluid, the first fluid is a high humidity fluid, and the pollutant trapping layer of each of the composite hollow fiber membranes F is formed on an outer surface of the hollow fiber membrane. It may also be coated on.
- the first fluid introduced into the housing part 100 through the first fluid inlet 121 of the housing cap 120 on one side passes through the hollows of the composite hollow fiber membranes F of the hollow fiber membrane cartridge 200. It is discharged to the outside of the membrane humidifier through the first fluid outlet 122 of the housing cap 120 of the other side.
- the second fluid is supplied to the housing body 110 through the second fluid inlet 131 of the housing body 110, and then flows to the outside of the composite hollow fiber membranes (F), the housing body It is discharged to the outside through the second fluid outlet 132 of (110). At this time, the second fluid flows outside the composite hollow fiber membranes F and performs moisture exchange with the low humidity first fluid passing through the hollows of the composite hollow fiber membranes F.
- first fluid inlet 121 may be closer to the second fluid inlet 131 than the first fluid outlet 122, but the present invention is not limited thereto.
- 122 may be closer to the second fluid inlet 131 than to the first fluid inlet 121.
- water and DMAC were respectively prepared by mixing 50 wt%.
- the dope and the coagulating solution were injected into a double tubular nozzle to prepare a hollow fiber membrane.
- a cap for potting part is formed on both ends of the body portion, and the hollow fiber membrane
- the composition for potting was injected into the space between the spaces and the space between the hollow fiber membrane bundle and the body portion, and then cured and sealed.
- the end of the cured hollow fiber membrane potting composition was cut so that the end of the hollow fiber membrane bundle was exposed to the potting part cut to form a potting part to prepare a hollow fiber membrane cartridge.
- a membrane cap was manufactured by covering both ends of the housing with a housing cap.
- a coating mixture (viscosity: 380 cps) in which 5% by weight of poly (perfluorosulfonic acid) was dispersed in IPA was passed into the film humidifier so as to pass through the hollows of the hollow fiber membranes of the membrane humidifier. After circulating for 20 minutes at a flow rate of, it was dried for 8 hours at 40 °C to form a contaminant trapping layer on the inner surface of the hollow fiber membranes. At this time, the dry air of 40 °C, 7% humidity to the outside of the hollow fiber membrane was circulated together at a flow rate of 300 LPM.
- Each of the composite hollow fiber membranes thus prepared contained 10 wt% of the pollutant trapping layer with respect to the total weight of the composite hollow fiber membrane, and the thickness of the pollutant trapping layer was 8 ⁇ m.
- the average pore size of the hollow fiber membranes was 2,300 nm, the average pore size of the composite hollow fiber membranes was 2,100 nm, and the ratio of the average pore size of the composite hollow fiber membranes to the average pore size of the hollow fiber membranes was 91.3%.
- the porosity of the hollow fiber membrane was 80%, the porosity of the composite hollow fiber membrane was 77%, and the ratio of the porosity of the composite hollow fiber membrane to the porosity of the hollow fiber membrane was 96.2%.
- Example 1 Except for using charcoal (charcoal) as the pollutant collecting material in Example 1 was prepared in the same manner as in Example 1.
- Example 1 Except for using a sulfonated polyethersulfone (S-PES) sulfonated polyethersulfone as the pollutant trapping material in Example 1 was prepared in the same manner as in Example 1.
- S-PES sulfonated polyethersulfone
- Example 1 Except for forming a contaminant trapping layer on the inner surface of the hollow fiber membrane in Example 1 was prepared in the same manner as in Example 1.
- the average pore size of the hollow fiber membrane was 2,300 nm, the porosity of the hollow fiber membrane was 80%.
- the gas collection performance flowed air containing 1 ppm of NH 3 to the membrane humidifier, and measured the NH 3 concentration of air discharged through the membrane humidifier.
- the membrane humidifiers prepared in the examples have better gas collection performance than the membrane humidifiers prepared in the comparative example.
- the gas-gas humidification was performed by fixing at 70 degreeC and 90% of humidity, and fixing inside the hollow fiber membrane at the temperature of 40 degreeC and 10% of humidity.
- Humidification performance was measured by converting the temperature and humidity at the point where the air flowing inside the composite hollow fiber membrane / hollow fiber membrane is humidified (Dew Point) was measured, the results are shown in Table 2 below.
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Abstract
Description
배출 공기의 NH3 농도(ppm) | 가스 포집 효율(%) | |
실시예 1 | 0.1 ppm | 90 % |
실시예 2 | 0.28 ppm | 72 % |
실시예 3 | 0.11 ppm | 89 % |
비교예 1 | 0.96 ppm | 4 % |
비교예 1 | 실시예1 | 실시예2 | 실시예3 | |
가습성능(℃) | 58 | 58.5 | 58 | 58.9 |
Claims (17)
- 중공사막; 및상기 중공사막의 내표면(inner surface) 상에 코팅되어 있어 상기 중공사막의 중공(lumen)을 따라 흐르는 공기로부터 오염물질을 제거할 수 있는 오염물질 포집층(pollutant entrapping layer) - 상기 오염물질은 질소 산화물, 황산화물, 암모니아 또는 이들 중 2 이상의 혼합물을 포함함 -을 포함하는,복합 중공사막.
- 제 1 항에 있어서,상기 오염물질 포집층은 바이오차(biochar), 차콜(charcoal), 활성탄(active carbon), 또는 이들 중 2 이상의 혼합물을 포함하는,복합 중공사막.
- 제 1 항에 있어서,상기 오염물질 포집층은상기 복합 중공사막 전체 중량에 대하여 1 중량% 내지 50 중량%의 양으로 상기 복합 중공사막 내에 존재하는,복합 중공사막.
- 제 1 항에 있어서,상기 중공사막의 평균 기공 크기는 0.1 nm 내지 100,000 nm이고,상기 복합 중공사막의 평균 기공 크기는 0.05 nm 내지 90,000 nm이고,상기 중공사막의 평균 기공 크기에 대한 상기 복합 중공사막의 평균 기공 크기의 비율은 50 % 이상인,복합 중공사막.
- 제 1 항에 있어서,상기 중공사막의 다공도는 50 % 내지 90 %이고,상기 복합 중공사막의 다공도는 45 % 내지 85 %이고,상기 중공사막의 다공도에 대한 상기 복합 중공사막의 다공도의 비율은 94.4% 이상인,복합 중공사막.
- 중공사막을 준비하는 단계; 및상기 중공사막의 중공을 따라 흐르는 공기로부터 오염물질을 제거하기 위하여, 오염물질 포집 물질(pollutant entrapping material)을 포함하는 코팅 혼합물을 상기 중공사막의 내표면 상에 코팅하는 단계 - 상기 오염물질은 질소 산화물, 황산화물, 암모니아 또는 이들 중 2 이상의 혼합물을 포함함 -를 포함하는,복합 중공사막의 제조 방법.
- 제 6 항에 있어서,상기 코팅 혼합물은 상기 오염물질 포집 물질이 용매에 용해되어 있는 용액 또는 상기 오염물질 포집 물질이 분산매에 분산되어 있는 분산액인,복합 중공사막의 제조 방법.
- 제 6 항에 있어서,상기 코팅 혼합물은 상기 코팅 혼합물 전체 중량에 대하여 상기 오염물질 포집 물질을 1 중량% 내지 30 중량%로 포함하는,복합 중공사막의 제조 방법.
- 제 6 항에 있어서,상기 코팅 단계는 상기 코팅 혼합물을 상기 중공사막의 중공을 통해 순환시키는 단계를 포함하는,복합 중공사막의 제조 방법.
- 제 9 항에 있어서,복수개의 상기 중공사막들로 중공사막 다발을 준비하는 단계;제 1 유체가 상기 중공사막들의 중공들을 따라 흐르고 제 2 유체가 상기 중공사막들의 외부로 흐를 수 있도록 상기 중공사막 다발이 내부에 배치된 중공사막 모듈을 제조하는 단계를 더 포함하며,상기 코팅 단계는 상기 중공사막 모듈 제조 후에 수행되는,복합 중공사막의 제조 방법.
- 제 9 항에 있어서,상기 코팅 혼합물의 점도는 50 내지 10,000 cps이고,상기 코팅 혼합물은 0.1 내지 30 LPM의 유량으로 순환되는,복합 중공사막의 제조 방법.
- 제 9 항에 있어서,상기 코팅 단계는, 상기 코팅 혼합물의 순환 단계 후에, 건조 공기를 상기 중공사막들의 외부를 통해 순환시키는 단계를 더 포함하는,복합 중공사막의 제조 방법.
- 제 12 항에 있어서,상기 건조 공기의 순환 단계는 10 내지 150 ℃의 건조 공기를 1 내지 1,000 LPM의 유량으로 순환시킴으로써 수행되는,복합 중공사막의 제조 방법.
- 복수개의 복합 중공사막들; 및상기 복합 중공사막들이 수용되는 바디부를 포함하며,상기 복합 중공사막들 각각은,중공사막; 및상기 중공사막의 내표면 상에 코팅되어 있어 상기 중공사막의 중공을 따라 흐르는 공기로부터 오염물질을 제거할 수 있는 오염물질 포집층 - 상기 오염물질은 질소 산화물, 황산화물, 암모니아 또는 이들 중 2 이상의 혼합물을 포함함 -을 포함하는,중공사막 카트리지.
- 제 1 유체가 유입되는 제 1 유체 유입구, 제 1 유체가 유출되는 제 1 유체 유출구, 제 2 유체가 유입되는 제 2 유체 유입구, 그리고 제 2 유체가 유출되는 제 2 유체 유출구를 포함하는 하우징부; 및상기 제1 및 제2 유체들 사이의 수분 교환을 각각 수행하는 복수개의 복합 중공사막들 - 상기 제1 유체는 상기 복합 중공사막들의 중공들을 따라 흐르고 상기 제2 유체는 상기 복합 중공사막들의 외부를 흐를 수 있도록 상기 복합 중공사막들이 상기 하우징부 내부에 설치됨 -을 포함하며,상기 제1 및 제2 유체들 중 하나는, 외부로부터 공급되어 상기 수분 교환을 통해 가습되는 저습 공기이고,상기 복합 중공사막들 각각은,중공사막; 및상기 중공사막의 외표면과 내표면 중 상기 저습 공기가 흐르는 어느 하나 상에 코팅되어 상기 저습 공기와 직접 접촉함으로써 상기 저습 공기로부터 오염물질을 제거할 수 있는 오염물질 포집층 - 상기 오염물질은 질소 산화물, 황산화물, 암모니아 또는 이들 중 2 이상의 혼합물을 포함함 -을 포함하는,연료 전지 막가습기.
- 제 15 항에 있어서,상기 오염물질 포집층은 바이오차, 차콜, 활성탄, 또는 이들 중 2 이상의 혼합물을 포함하는,연료 전지 막가습기.
- 제 15 항에 있어서,상기 복합 중공사막들의 중공들을 따라 흐르는 상기 제1 유체가 상기 저습 공기이고,상기 오염물질 포집층은 상기 중공사막의 내표면 상에 코팅된,연료 전지 막가습기.
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US15/734,266 US11876259B2 (en) | 2018-06-12 | 2019-06-12 | Composite hollow fiber membrane, manufacturing method therefor, hollow fiber membrane cartridge including same, and fuel cell membrane humidifier |
JP2020564318A JP7224372B2 (ja) | 2018-06-12 | 2019-06-12 | 複合中空糸膜、その製造方法、これを含む中空糸膜カートリッジ及び燃料電池膜加湿器 |
EP19819113.2A EP3812035A4 (en) | 2018-06-12 | 2019-06-12 | HOLLOW FIBER COMPOSITE MEMBRANE, MANUFACTURING PROCESS THEREOF, HOLLOW FIBER MEMBRANE CARTRIDGE THEREOF AND FUEL CELL MEMBRANE HUMIDIFIER |
CN201980039517.2A CN112292198B (zh) | 2018-06-12 | 2019-06-12 | 复合中空纤维膜、其制造方法、包括其的中空纤维膜盒及燃料电池膜加湿器 |
JP2023016252A JP2023058569A (ja) | 2018-06-12 | 2023-02-06 | 複合中空糸膜、その製造方法、これを含む中空糸膜カートリッジ及び燃料電池膜加湿器 |
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KR10-2018-0067556 | 2018-06-12 | ||
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EP (1) | EP3812035A4 (ko) |
JP (2) | JP7224372B2 (ko) |
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EP3905400A4 (en) * | 2018-12-28 | 2022-10-19 | Kolon Industries, Inc. | MEMBRANE HUMIDIFIER FOR FUEL CELL |
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KR20220096814A (ko) | 2020-12-31 | 2022-07-07 | 코오롱인더스트리 주식회사 | 연료전지 막가습기 |
KR20220127988A (ko) | 2021-03-12 | 2022-09-20 | 코오롱인더스트리 주식회사 | 연료전지 막가습기 |
KR20220127987A (ko) | 2021-03-12 | 2022-09-20 | 코오롱인더스트리 주식회사 | 연료전지 막가습기 |
KR20220168468A (ko) | 2021-06-16 | 2022-12-23 | 코오롱인더스트리 주식회사 | 연료전지 막가습기 |
KR20220168470A (ko) | 2021-06-16 | 2022-12-23 | 코오롱인더스트리 주식회사 | 연료전지 막가습기 |
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CN112292198B (zh) | 2023-04-04 |
JP7224372B2 (ja) | 2023-02-17 |
EP3812035A1 (en) | 2021-04-28 |
US11876259B2 (en) | 2024-01-16 |
JP2023058569A (ja) | 2023-04-25 |
KR20190140855A (ko) | 2019-12-20 |
EP3812035A4 (en) | 2022-03-09 |
JP2021523827A (ja) | 2021-09-09 |
KR102490366B1 (ko) | 2023-01-20 |
CN112292198A (zh) | 2021-01-29 |
US20210154624A1 (en) | 2021-05-27 |
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