A monolithic fuel cell cooler assembly with reactant flow fields integrated therein has a single consistent composition throughout which resists acid absorption sufficiently to render acid impermeable graphite or carbon separator plate and edge layers unnecessary, and permits integration of reactant gas flow fields with the cooler plate.
In low temperature stationary fuel cell power plants, acid electrolytes are quite common. One factor that has to be accommodated is the migration of acid from one fuel cell into the next. This has resulted in the use of acid-impermeable graphite or carbon separator plates disposed at opposite surfaces of cooler plates, or centrally within integral separator plate assemblies. In addition, cooler plates used in acid electrolyte fuel cells have had acid-impermeable edge protection layers on both edges of the cooler array, in order to avoid corrosion of the metallic coolant tube material.
In order to bond metal coolant tubes with components in typical contemporary cooler plates, the exterior surface of the coolant tubes have been roughened by flame spraying, sand blasting or otherwise. Roughening of the surface is expensive. In order to protect the coolant plate, and particularly the coolant tube, from corrosion by the acid electrolyte, contemporary cooler plates have required acid edge protection layers or films, which may have taken the form of a tape of fluorinated ethylene propylene polymer or polytetrafluoroethylene, with an adhesive layer which joins the tape to the edge of the plate; this is also expensive.
Exemplary prior systems are disclosed in U.S. Pat. Nos. 4,929,517, 5,558,955 and 6,050,331, and in patent publication US 2011-017749, all incorporated herein by reference.
Contemporary cooler plates which are disposed between flow field plates are typically not bonded or adhered to the adjacent flow field plates. While it is desirable in liquid electrolyte fuel cells to have the electrode substrates be porous and hydrophilic, so that they can act as electrolyte storage volumes, the electrolyte penetration thereof requires that there be liquid impermeable separator plates between the electrode substrates and the cooler plate to prevent coolant tube corrosion. Typically, the acid impervious graphite or carbon separator plates are bonded to the cooler plates.
The contemporary cooler plates and associated flow field plates for liquid electrolyte fuel cells are therefore composed of many parts requiring many procedural steps for their manufacture. This is not only expensive, but it also increases the bulk of each section of the fuel cell stack.
A composite cooler and reactant flow field plate for liquid electrolyte fuel cells in accordance with the modality herein includes a uniform composition of flake graphite and polymer binder. Because the cooler plate is formulated with a consistent monolithic composition comprising between about 80 wt. % and about 85 wt. % flake graphite, balance polymer binder, the cooler plate does not require, and therefore is devoid of any acid-resisting edge protection layers or separator plate layers. Reactant flow fields for adjacent fuel cells are integral with the cooler plate, being formed in portions of the cooler plate which consist of very dense flaked graphite and hydrophobic thermoplastic polymer; the cooler plate according to the present modality is therefore devoid of acid-resisting graphite or carbon separator plates or layers adjacent to the reactant flow fields.
A method of forming the composite plate includes depositing a first volume of the aforementioned flake graphite and polymer binder composition, which may or may not include a dense, compacted preform, in the bottom of a mold, placing a coolant tube array on said first volume, depositing a powder of the aforementioned composition around and above the coolant tube array, depositing a second volume of said composition, which may or may not include a dense compacted preform, above said powder, placing a mold plunger on top of said second volume, heating the mold content above the melting temperature of the polymer at a pressure of about 625 psi (431 kPa) for about 5 or more minutes, cooling the mold content to at least the solidification temperature of the polymer while still under said pressure, further cooling the mold content, disassembling the mold and removing the formed composite plate.
Other variations will become more apparent in the light of the following detailed description of exemplary embodiments, as illustrated in the accompanying drawings.
Referring to
Referring to
In
In
Instead of compacted preforms, the aforementioned mixture may be used in powdered form at the bottom of the mold and in all the volume above the coolant tube.
In
During the molding process, the preform density increases from about 1.8 gm/ml (about 1.03 oz/cu in) to about 2.1 gm/ml (about 1.2 oz/cu in). The melting of the polymer, and its bonding with the flake graphite under pressure, causes the highly hydrophobic nature of the composite plate, which provides superior resistance to acid penetration.
Instead of being machined upon completion of the composite cooler plate, the reactant gas flow field channels 31, 32 may be molded into the preforms 15, 23 as the composite plate is formed in
The modality herein is applicable to liquid electrolyte fuel cells, particularly acid electrolyte fuel cells. Phosphoric acid is currently in common use, but the modality herein is applicable to other acid electrolytes, such as fluoroborate acid, which systems would operate at pressures and temperatures similar to those of phosphoric acid systems.
Since changes and variations of the disclosed embodiments may be made without departing from the concept's intent, it is not intended to limit the disclosure other than as required by the appended claims.
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/US2011/001806 | 10/25/2011 | WO | 00 | 4/22/2014 |
Publishing Document | Publishing Date | Country | Kind |
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WO2013/062503 | 5/2/2013 | WO | A |
Number | Name | Date | Kind |
---|---|---|---|
4478918 | Ueno | Oct 1984 | A |
4929517 | Luoma et al. | May 1990 | A |
5558955 | Breault et al. | Sep 1996 | A |
6050331 | Breault | Apr 2000 | A |
20110177419 | Luoma | Jul 2011 | A1 |
Number | Date | Country |
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63128562 | Jun 1988 | JP |
2003077485 | Mar 2003 | JP |
2006156173 | Jun 2006 | JP |
2010123478 | Oct 2010 | WO |
2010123479 | Oct 2010 | WO |
Entry |
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Sandra Curtin—Different Types of Fuel Cells (Apr. 1, 2006) AltEnergyMag. |
JP 2003-077485—Fuel cell searator and its manufacturing method (AIPN translation). |
English machine translation of Seki (JP 63128562 A) provided herein (Year: 1998). |
International Search Report and Written Opinion for International Application No. PCT/US2011/001806 dated May 25, 2012. |
Number | Date | Country | |
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20140295300 A1 | Oct 2014 | US |