The present invention relates to a reformer module for a fuel cell system and in particular to a reformer for a solid oxide fuel cell system.
Methane steam reforming is a highly endothermic reaction and results in localised cooling in the reformer unit.
At the temperatures used for steam reforming in a solid oxide fuel cell the kinetics of the steam reforming reaction are extremely rapid. A problem with indirect internal steam reforming in a solid oxide fuel cell is the mismatch between the activity of the steam reforming catalyst and the heat available from the solid oxide fuel cells. As a result a large temperature gradient may be produced along the length of the reformer unit.
This problem may be reduced by using only a small fraction of the available catalyst activity. This may be achieved practically by providing a non-uniform distribution of the catalyst or by providing a diffusion barrier on the surface of the catalyst. Traditionally a catalyst layer is provided on the outer surface of a pellet and a barrier layer is provided on the catalyst layer or a catalyst slurry layer is provided on the interior surface of a hollow support and a barrier layer is provided on the catalyst layer. In both these cases the application of a catalyst or a barrier layer is extremely difficult due to the uneven nature of the surface of the pellet and hollow support and in the case of the hollow support it is extremely difficult to coat the interior surface of the hollow support. Furthermore, the non-uniform distribution of the catalyst layer is also extremely difficult in both these cases.
Accordingly the present invention seeks to provide a novel reformer module, which reduces, preferably overcomes, the above-mentioned problems.
Accordingly the present invention provides a reformer module comprising a hollow support member having at least one passage extending longitudinally therethrough, means to supply a fuel to the at least one passage, the hollow support member having an external surface, a reforming catalyst layer arranged on at least a portion of the external surface of the hollow support member and a gas tight sealing layer arranged on the catalyst layer and the external surface of the hollow support member other than the at least a portion of the external surface of the hollow support member.
Preferably a barrier layer is arranged on the at least a portion of the external surface of the hollow support member and the catalyst layer is arranged on the barrier layer.
Preferably the barrier layer is arranged on substantially the whole of the external surface of the hollow support member.
Preferably a catalyst layer is arranged on the barrier layer at each of a plurality of regions of the external surface of the hollow support member, the sealing layer is arranged on the catalyst layer at each of the regions of the external surface of the hollow support member having a catalyst layer and on the barrier layer and the hollow support member at regions of the external surface of the hollow support member other than the plurality of regions.
The catalyst layers at the plurality of regions may be spaced apart longitudinally of the hollow support member. The catalyst layers at the regions may have different areas. The catalyst layers at the plurality of regions may increase in area longitudinally from a first end to a second end of the hollow support member.
Alternatively the catalyst layer may be arranged on substantially the whole of the barrier layer, the barrier layer has a different thickness at different regions. The barrier layer may decrease in thickness from a first end to a second end of the hollow support member.
Alternatively the barrier layer may have apertures therethrough and the total cross-sectional area of the apertures in the barrier layer is different at different regions. The total cross-sectional area of the apertures in the barrier layer at the different regions may increase from a first end to a second end of the hollow support member. The dimensions of the apertures may increase and/or the number of apertures may increase.
Alternatively the catalyst layer has a different activity at different regions. The catalyst layers at the different regions may increase in activity from a first end to a second end of the hollow support member.
Preferably the first end is an inlet for a hydrocarbon fuel to be reformed and the second end is an outlet for reformed fuel.
Preferably the hollow support member comprises a plurality of longitudinally extending passages.
Preferably the hollow support member is porous.
Alternatively the hollow support member is non-porous and has a plurality of apertures extending therethrough.
The total cross-sectional area of the apertures in the hollow non-porous support member may be different at different regions.
The total cross-sectional area of the apertures in the hollow non-porous support member at the different regions may increase from a first end to a second end of the hollow support member. The dimensions of the apertures may increase and/or the number of apertures may increase.
The present invention will be more fully described by way of example with reference to the accompanying drawings in which:
A reformer module 10, as shown in
It is to be noted that the hollow porous support member 12 has two substantially flat parallel external surfaces 20A and 20B, as shown in
The porous barrier layer 22 is a diffusion barrier layer to control the rate of diffusion of the hydrocarbon fuel from the passages 14 to the catalyst layer 24. The hollow porous support member 12 comprises for example magnesium aluminate spinel, yttria stabilised zirconia, silicon carbide or other suitable ceramic. The porous barrier layer 22 comprises for example yttria-stabilised zirconia. The catalyst layer 24 comprises for example rhodium, nickel or other suitable reforming catalyst and preferably comprises about 1 wt % of the catalyst material dispersed in a suitable material, for example yttria-stabilised zirconia. The sealing layer 26 is gas tight and comprises for example a glass or dense non-porous yttria-stabilised zirconia.
The porous barrier layer 22 and the catalyst layer 24 may be deposited by screen-printing, ink-jet printing, brush painting, dipping or slurry coating.
In operation a hydrocarbon fuel, for example methane, is supplied to the first end 16 of the reformer module 10. The hydrocarbon fuel flows through the passages 14 from the first end 16 to the second end 18 of the reformer module 10. The hydrocarbon fuel diffuses through the hollow porous support member 12 and through the porous barrier layer 22 to the catalyst layer 24. The hydrocarbon fuel is reformed in the catalyst layer 24 and the products of the reforming reaction, hydrogen, carbon monoxide, carbon dioxide etc diffuse through the porous barrier layer 22 and the hollow porous support member 12 to the passages 14. The products of the reforming reaction flow through the passage 14 and out of the second end 18 of the reformer module 10 and are supplied to a solid oxide fuel cell system (not shown).
A further embodiment of a reformer module 10B according to the present invention is shown in
Another embodiment of a reformer module 10C according to the present invention is shown in
The porous barrier layer 22 may decrease in thickness in a stepped manner rather than by a continuous decrease in thickness. The porous barrier layer 22 may be produced by initially dipping substantially the full length of the hollow porous support member 12 into a tank containing the barrier layer material, yttria stabilised zirconia, so that the whole of the external surface of the hollow porous support member 12 is covered by the porous barrier layer 22. Then the hollow porous support member 12 is dipped sequentially into the tank containing the barrier layer material, yttria stabilised zirconia, by progressively shorter distances so that less and less of the length of the hollow porous support member 12 is covered by the porous barrier layer 22 to produce the stepped change in thickness of the porous barrier layer 22.
A further alternative is to dip the hollow porous support member 12 sequentially into tanks containing barrier layer materials with different compositions.
A further embodiment of a reformer module 10D according to the present invention is shown in
Alternatively the catalyst layer 24 may have a lesser activity at the first end 16 than the second end 18 of the reformer module 10.
A further embodiment of a reformer module 10E according to the present invention is shown in
It may be possible to dispense with the barrier layer in some circumstances for example in
The advantages of the present invention are that by providing the catalyst layer on the exterior surface of the hollow support member, the distribution of the catalyst may be more precisely controlled and thus a non-uniform distribution of catalyst may be achieved. Furthermore, a barrier layer may also be provided more easily between the hollow support member and the catalyst layer, the distribution of the barrier layer may be more precisely controlled and thus a non-uniform distribution of the barrier layer may be achieved. The exterior surfaces of the hollow support member may be maintained uniform and flat, facilitating an even and continuous deposited layer. Also the layers may be more easily inspected for flaws, cracks and thickness etc. There is only the sealing layer to provide between the external surroundings, which provide the heat for the reforming reaction, and the catalyst layer where the reforming reaction occurs and this provides a low thermal barrier to the transfer of heat to the catalyst layer.
As a further possibility the reformer module may itself form a part of the solid oxide fuel stack as described in published International patent application WO03010847A published 6 Feb. 2003. In that case a portion of one or both of the external surfaces of the reformer module has a barrier layer, a catalyst layer and a sealing layer and the remainder of one or both of the external surfaces may also have one or more solid oxide fuel cells.
Although the present invention has been described with reference to use with solid oxide fuel cells, it may be equally possible to use the present invention with other fuel cells and generally for steam reforming or catalytic combustion.
Number | Date | Country | Kind |
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0317575.9 | Jul 2003 | GB | national |
This is a divisional of U.S. patent application Ser. No. 11/312,378, filed 21 Dec. 2005 and currently U.S. Pat. No. 7,749,465, which is a continuation of International Application Number PCT/GB2004/002811, filed 30 Jun. 2004 and designating the United States, which claims priority of GB 0317575.9, filed 26 Jul. 2003.
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0435642 | Jul 1991 | EP |
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Number | Date | Country | |
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20100135872 A1 | Jun 2010 | US |
Number | Date | Country | |
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Parent | 11312378 | Dec 2005 | US |
Child | 12689469 | US |
Number | Date | Country | |
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Parent | PCT/GB2004/002811 | Jun 2004 | US |
Child | 11312378 | US |