Patent Application
20080075940
The invention relates to a conductive nonwoven fabric.
Conductive nonwoven fabrics are used as gas diffusion layers in membrane electrode assemblies (MEAs) for PEM (proton exchange membrane) fuel cells and should be electron conductive and gas-permeable. These nonwoven fabrics should also have channel structures for transporting away water that is formed during a reaction when operating fuel cells, and should possess an inherent rigidity at a limited thickness. Furthermore, these nonwoven fabrics should have a good surface smoothness at least on one side.
Two-dimensional textile materials, such as conductive woven fabrics or wet-laid nonwoven fabrics, may be used as starting materials for gas diffusion layers. Nonwoven fabrics having a thickness of 0.3 to 0.5 mm are referred to in Japanese Patent Application No. 06/123050, these fabrics including carbonizable polymer fiber materials, such as polyacrylic nitrile (PAN) or oxidized polyacrylic nitrites, with a mass per unit area of 100 to 200 g/m2. To achieve the required electrical conductivity, these textile fabrics are carbonized at temperatures between 1000 and 2100° C., whereby a carbon content of approximately 90 to 96% is achieved. A reduction in mass per unit area by 30 to 60 weight-percent is connected with the carbonization, i.e. graphitization process. Usually, these fabrics, which are now conductive, are rigid and demonstrate a relatively open structure. The woven fabrics or nonwoven fabrics may be impregnated or coated with dispersions of conductive particles, such as graphite or carbon black, to achieve the required rigidity and to improve the conductivity in the X, Y, and Z direction, and subsequently to press them to achieve a high degree of surface smoothness.
Furthermore, Japanese Patent Application No. 10/777624 and Japanese Patent Application No. 10/777625 refer to the production of gas diffusion layers directly from carbon fibers in a wet-laying process, so that subsequent carbonization of the precursor fibers is unnecessary. In this connection, polyvinyl alcohol (PVA) solutions or polyethylene terephthalate (PET) substrates may be used as a binder for the carbon fibers. Subsequently, the hydrophobic properties of the gas diffusion layer may still be adjusted by finishing them with a hydrophobization agent, such as polytetrafluoroethylene (PTFE) dispersions and subsequent sintering.
It is believed that methods for the production of gas diffusion layers for PEM fuel cells are disadvantageous in that they may not be rolled up for transport and processing and must be filled with conductive fillers, to achieve the required conductivity values.
It is an object of the present invention to provide a conductive nonwoven fabric that overcomes the disadvantages described above.
To achieve this object, a conductive nonwoven fabric is carbonized and/or graphitized and possesses a bending rigidity <8 taber, a density of 0.1 g/m3 to 0.5 g/m3, a thickness of 80 μm, to 500 μm, and an electrical conductivity of 10 to 300 S/cm in the nonwoven fabric strip and 30 to 220 S/cm2 perpendicular to the nonwoven fabric strip.
An exemplary conductive nonwoven fabric according to the invention is obtained from preoxidized fibers as a precursor stage for carbon fibers that are mixed, for example, with up to 30 wt. % of a precursor fiber that serves as a binder fiber, as well as up to 30 wt. % of a water-soluble fiber with a fiber titer of 0.5 to 6.7 dtex, to form a fiber fleece with a mass per unit area of 60 to 300 g/m2, by bonding of the fiber fleece with high-pressure fluid jets at pressures of 100 to 300 bar, compression of the bonded fiber fleece by 50 to 90% of its starting thickness by calendaring, and carbonization and/or graphitization under an inert gas atmosphere, at 800° C. to 2500° C. The conductive nonwoven fabric obtained in this manner demonstrates a channel structure in the direction of the layer thickness of the nonwoven fabric. The preoxidized fibers and, if applicable, the binder fibers and water-soluble fibers, are mixed homogeneously and deposited to form a fiber sheet. The fiber sheet, with a mass per unit area of 30 to 300 g/m2, is passed to a bonding unit, in which the fibers are swirled and intertangled by high-energy water jets, at pressures of 100 to 300 bar. After this treatment, a part of the fibers demonstrates an orientation in the direction of the Z direction (thickness) of the nonwoven fabric.
For example, the conductive nonwoven fabric may be one in which 80 to 90 wt.-% of a mixture of binder fibers and preoxidized fibers in a weight ratio of 0:1 to 1:3 and 10 to 20 wt.-% of a water-soluble fiber with a fiber titer of 0.8 to 3.3 dtex are used. This composition of the fibers and their fineness result in conductive nonwoven fabrics with a porosity of 70 to 95. For example, the conductive nonwoven fabric may be one in which two different water-soluble fibers are used, one of which is water-soluble at temperatures of 10 to 40° C. and the other of which is water-soluble at temperatures of 80 to 120° C. By using fibers with different water solubilities, the fibers in the temperature range of 10 to 40° C. are already dissolved out of the fiber fleece during the water-jet bonding process, and defined channels are formed in the nonwoven fabric layer, allowing improved gas permeability and improved removal transport of the water of reaction in the gas diffusion layer produced from them. The fibers that are not soluble in water until a temperature range of 80 to 120° C. remain in the bonded nonwoven fabric and become binder fibers in the wet state, because of their stickiness. For this purpose, the nonwoven fabric is passed through and compressed by a calendar while it is still wet.
For example, the conductive nonwoven fabric may be one in which the ratio of the water-soluble fibers relative to one another is 3:1 to 1:3. The rigidity of the gas diffusion layer and its porosity may be adjusted with this ratio.
A conductive nonwoven fabric including several fiber layers with different pore sizes may be used, in which the fibers of the individual layers possess different titers. The progressive build-up of the conductive nonwoven fabric from several fiber layers promotes the transport reaction to the proton exchange membrane and the removal transport of the water of reaction that is formed.
Conductive nonwoven fabrics, in which partially crosslinked phenolic resin fibers, polyester and/or polypropylene fibers are used as the precursor fibers, homopolymers, copolymers, and/or terpolymers of PAN (polyacrylic nitrile) fibers, cellulose fibers and/or phenolic resin fibers are used as the preoxidized fibers, and PVA (polyvinyl alcohol) fibers are used as the water-soluble fibers may be used. The gas diffusion layer obtained from a nonwoven fabric made of these fibers may be carbonized well and easily adjusted with regard to its pore distribution and its rigidity.
A conductive nonwoven fabric that is hydrophobized by application of a hydrophobization agent, such as PTFE (polytetrafluoroethylene) may also be used. The transport processes at the phase border surfaces may be further improved by hydrophobization.
According to the invention, the conductive nonwoven fabric is produced in such a manner that
For example, production may be performed in that in step
In step e) at least two nonwoven fabric layers are calendared together.
The invention will be explained in greater detail below, using examples.
A preoxidized PAN fiber (oxidized PAN fiber—OPF) with a fiber titer of 0.8 dtex and a fiber length of 60 mm is laid on a carding system to form a fiber fleece with a mass per unit area of 100 g/m2. The fiber fleece is passed to a bonding unit, in which the fibers are tanglelaced and intertangled with one another by high-energy water jets on both sides, at pressures of approximately 100 bar in the first step and approximately 170 bar in the second step, in each instance. The nonwoven fabric is predried to a residual moisture of 15 to 20%. While still wet, the nonwoven fabric is passed to a felt band calendar and compressed at a temperature of approximately 220° C. and at 20 bar. As a result of the calendaring process, the thickness of the water-jet-bonded nonwoven fabric is reduced from 0.8 mm to a thickness of 0.4 to 0.5 mm. Subsequently, the nonwoven fabric is passed to a carbonization unit, in which carbonization occurs under a nitrogen atmosphere at approximately 1000 to 1400° C. The resulting conductive nonwoven fabric has a crosswise conductivity, i.e., in the layer plane, of 12 S/cm in the machine direction, 18 S/cm crosswise to the machine direction, at a bending rigidity of <1 taber and an air permeability of 6.0 l/m2sPa, and its through conductivity, i.e. perpendicular to the layer plane, is 90 S/cm2, where this value was determined at a surface pressure of 4.07 bar. Its density is 0.16 g/cm3, the porosity is 91%, and the average pore diameter is 25 μm.
A two-layer fiber fleece made up of a first fleece layer with a mass per unit area of 50 g/m2, made up of 80 wt.-% OPF with a fiber titer of 1.2 dtex and a fiber length of 60 mm, as well as 20 wt.-% of a TTP fiber (textile tow precursor) with a fiber titer of 1.7 dtex and a fiber length of 40 mm, and a second fleece layer with a mass per unit area of 50 g/m2, made up of 80 wt.-% OPF with a fiber titer of 0.8 dtex and a fiber length of 60 mm, as well as 20 wt.-% of a TTP fiber with a fiber titer of 0.8 dtex and a fiber length of 40 mm, which were cross-laid on a carding system, is passed to a bonding unit, in which the fibers are tanglelaced and intertangled with one another by high-energy water jets on both sides, at pressures of approximately 120 bar in the first step and approximately 190 bar in the second step, in each instance. The nonwoven fabric is predried to a residual moisture of approximately 10%. While still in the wet state, the nonwoven fabric is passed to a roller calendar with a steel roller and a roller coated with cotton, where the temperature of the steel roller was approximately 210° C. and that of the roller coated with cotton was approximately 150° C., and compressed at a line pressure of 80 kp/cm2. As a result of the calendaring process, the thickness of the water-jet-bonded nonwoven fabric is reduced from 0.8 mm to a thickness of 0.16 mm. Subsequently, the nonwoven fabric is passed to a carbonization unit, in which carbonization occurs under a nitrogen atmosphere at approximately 1000 to 1400° C. The resulting conductive nonwoven fabric demonstrates a crosswise conductivity, i.e. in the layer plane, of 54 S/cm in the machine direction, 54 S/cm crosswise to the machine direction, at a bending rigidity of 1 taber and an air permeability of 2 l/m2sPa, and its through conductivity, i.e. perpendicular to the layer plane, is 120 S/cm2, where this value was determined at a surface pressure of 4.07 bar. Its density is 0.32 g/cm3, the porosity is 82%, and the average pore diameter is 15 μm.
A preoxidized PAN fiber (oxidized PAN fiber—OPF) with a fiber titer of 0.8 dtex and fiber lengths of 60 mm is laid on a carding system to form a fiber fleece with a mass per unit area of 100 g/m2. The fiber fleece is passed to a bonding unit in which the fibers are tanglelaced and intertangled with one another by high-energy water jets on both sides, at pressures of approximately 100 bar in the first step and approximately 170 bar in the second step, in each instance. The nonwoven fabric is predried to a residual moisture of 15 to 20%. While still wet, the nonwoven fabric is passed to a calendar made up of a steel roller and a plastic roller and compressed at a temperature of approximately 350° C. and at 250 kp/cm2. As a result of the calendaring process, the thickness of the water-jet-bonded nonwoven fabric is reduced from 0.9 mm to a thickness of 0.14 mm. Subsequently, the nonwoven fabric is passed to a carbonization unit in which carbonization occurs under a nitrogen atmosphere at approximately 1000 to 1400° C. The resulting conductive nonwoven fabric demonstrates a crosswise conductivity, i.e. in the layer plane, of 93.7 S/cm in the machine direction, 73 S/cm crosswise to the machine direction, at a bending rigidity of <1 taber and an air permeability of 1.0 l/m2sPa, and its through conductivity, i.e. perpendicular to the layer plane, is 195 S/cm2, where this value was determined at a surface pressure of 4.07 bar. Its density is 0.43 g/cm2, the porosity is 78%, and the average pore diameter is 7 μm.
| Number | Date | Country | Kind |
|---|---|---|---|
| 10050512.0 | Oct 2000 | DE | national |
This application is a continuation of U.S. application Ser. No. 10/149,398 filed Sep. 30, 2002 and published Jun. 12, 2003 as United States Patent Application Publication No. US2003/0109189, which is a National Stage Completion of PCT/EP01/11194 filed Sep. 27, 2001, which claims priority to DE 100 50 512.0 filed Oct. 11, 2000, the teachings of which are incorporated herein by reference.
| Number | Date | Country | |
|---|---|---|---|
| Parent | 10149398 | Sep 2002 | US |
| Child | 11834547 | Aug 2007 | US |
