Title of Invention | A METHOD FOR CONVERTING FUEL AND OXIDANT INTO REFORMATE IN A REFORMER |
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Abstract | The invention relates to a reformer for reacting fuel (12) and oxidant (16, 18, 20) to reformate (22). Said reformer comprises an oxidizing zone (24) and a reforming zone (26) A mixture of fuel (12) and oxidant (16, 18, 20) is delivered to the oxidizing zone (24) and is delivered at least in part to the reforming zone (26) following at least partial oxidation of the fuel (12). According to the invention, fuel (14) can be additionally delivered to the reforming zone (26) while heat (28) can be supplied to the reforming zone (26). The invention further relates to a method for reacting fuel (12) and oxidant (16, 18, 20) to reformate(22). |
Full Text | Reformer and method for converting fuel and oxidant into reformate The invention relates to a reformer for converting fuel and oxidant into reformate, comprising an oxidation zone and a reforming zone, wherein a mixture of fuel and oxidant may be supplied to the oxidation zone, and the mixture may be supplied at least partially to the reforming zone upon an at least partial oxidation of the fuel. The invention relates further to a method for converting fuel and oxidant into reformate in a reformer having an oxidation zone and a reforming zone, wherein a mixture of fuel and oxidant is supplied to the oxidation zone, the mixture being supplied at least partially to the reforming zone upon an at least partial oxidation of the fuel. Generic reformers and generic methods provide numerous fields of application. In particular, they serve for supplying a fuel cell with a hydrogen-rich gas mixture, from which electric energy may be generated on the basis of electrochemical processes. Such fuel cells are employed for example in the automotive field as auxiliary power sources, so called APUs ("auxiliary power unit11) . The reforming process for converting fuel and oxidant into reformate may proceed according to various concepts. For example, the catalytic reforming is known, in which part of the fuel is oxidized in an exothermic reaction. This cata- lytic reforming has the drawback of a high heat generation which may irreversibly harm the system components, in particular the catalytic converter. Another possibility for generating reformate from hydrocarbons is the "steam-reforming". In this process, hydrocarbons are converted within an endothermic reaction into hydrogen by the aid of water vapor. A combination of these both concepts, that is, the reforming on the basis of an exothermic reaction and the production of hydrogen by means of an endothermic reaction in which the energy for steam-reforming is extracted from the combustion of hydrocarbons, is called an autothermic reforming. Herein, the additional drawbacks arise that a possibility for supplying water has to be provided. High temperature gradients between the oxidation zone and the reforming zone constitute further problems in the temperature management of the entire system. An example for a reformer having an oxidation unit which is separated from a reforming unit is given in DE 199 43 248 Al. The invention is based on the object to provide a reformer and a method for converting fuel and oxidant into reformate, in which the mentioned problems are overcome at least partially and in which, in particular, problems due to high temperatures and large temperature gradients do not occur, respectively. This object is solved with the features of the independent claims. Advantageous embodiments of the invention are defined in the dependent claims. The invention is established beyond the generic reformer in that fuel may additionally be supplied to the reforming zone, and in that heat may be supplied to the reforming zone. The additionally supplied fuel thus forms together with the exhaust gas from the oxidation zone the starting gas mixture for the reforming process. Due to the mixing of the fuel with the exhaust gas, a small A-value is provided (for example A = 0.4), and an endothermic reforming reaction can take place by supplying heat. In this context it is especially beneficial that heat from the exothermic oxidation within the oxidation zone may be supplied to the reforming zone. The heat energy resulting from the oxidation zone is thus converted in the course of the reforming reaction such that the net heat generation of the entire process does not lead to problems in the temperature management of the reformer. Advantageously it is provided that the reforming zone comprises an oxidation supply through which oxidant may be additionally supplied. In this manner a further parameter for influencing the reforming is provided, in order to optimize it. The invention is in a very beneficial manner further developed in that the additional fuel may be supplied to an injection and mixture forming zone and in that the additional fuel can flow from the injection and mixture forming zone into the reforming zone. This injection and mixture forming zone is thus arranged upstream of the reforming zone such that the reforming zone is provided with a well mixed starting gas for the reforming reaction. In this context it is especially beneficial that the additional fuel is at least partially evaporated by the thermal energy of the gas mixture exiting the oxidation zone. Thus the reaction heat from the oxidation may be utilized in a beneficial manner also for the evaporation process of the fuel. Further, it may be beneficial that the gas mixture generated in the oxidation zone may be partially supplied to the reforming zone, bypassing the injection and mixture forming zone. Thereby, a further possibility for influencing the reforming process is provided such that a further improvement of the reformate exiting the reformer can be achieved with regards to its usage. The invention is established beyond the generic method in that additional fuel is supplied to the reforming zone, and in that heat is supplied to the reforming zone. In this manner the advantages and special characteristics of the reformer according to the present invention are achieved also in the course of a method. This also applies for the following especially preferred embodiments of the method according to the present invention. This method is beneficially further developed in that heat from the exothermic oxidation within the oxidation zone is supplied to the reforming zone. Further, it may be beneficial that the reforming zone comprises an oxidant supply through which additional oxidant is supplied. Within the scope of the method it is preferred that the additional fuel is supplied to an injection and mixture forming zone and that the additional fuel flows from the injection and mixture forming zone into the reforming zone. In relation to the method it is beneficially envisaged that the additional fuel is evaporated at least partially by the thermal energy of the gas mixture exiting the oxidation zone. Further, it can be provided that the gas mixture which is produced in the oxidation zone is partially supplied to the reforming zone, bypassing the injection and mixture forming zone. The invention is based on the conclusion that by separating the oxidation zone and the reforming zone and by mixing the exhaust gas from the oxidation zone with the additionally supplied fuel, a gas mixture may be produced which provides good preconditions with regards to the following reforming and/or which can be optimized by the further supply of exhaust gas and oxidant with regards to the reforming process . The invention is now explained by way of example referring to the accompanying drawings and the preferred embodiments. The drawings show in: Figure 1 a schematic diagram of a reformer according to the present invention; and in Figure 2 a flow chart for explaining a method according to the present invention. Figure 1 shows a schematic diagram of a reformer according to the present invention. Fuel 12 and oxidant 16 can be supplied to the reformer 10 through respective supplies. For the fuel 12, for example diesel may be considered, the oxidant 16 is usually air. The reaction heat generated instantaneous within the initial combustion may be partially discharged in an optionally provided cooling zone 36. The mixture then further proceeds into the oxidation zone 24 which can be realized as a pipe which is arranged within the reforming zone 26. In alternative embodiments, the oxidation zone is realized by multiple pipes or a specific pipe arrangement within the reforming zone 26. Within the oxidation zone, a conversion of fuel and oxidant within an exothermic reaction having X«l takes place. The gas mixture 32 produced thereby then enters an injection and mixture forming zone 30 in which it is mixed with injected fuel 14. The thermal energy of the gas mixture 32 can thereby support the evaporation of the fuel 14. Additionally, it can be provided that oxidant is supplied into the injection and mixture forming zone 30. The thus formed mixture then enters the reforming zone 26 where it is converted in an en- dothermic reaction, with for example A«0.4. The heat 28 needed for the endothermic reaction is discharged from the oxidation zone 24. For optimizing the reforming process, oxidant 18 may be additionally supplied into the reforming zone 26. Further, it is possible to directly supply part of the gas mixture 34 which is produced in the oxidation zone 24 to the reforming zone 26, bypassing the injection and mixture forming zone 30. The reformate 22 then flows out of the reforming zone 26 and is available for further utilization. Figure 2 shows a flow chart for explaining a method according to the present invention. In step SOI, fuel and oxidant is supplied to an oxidation zone. Thereafter, in step S02, an at least partial oxidation of the fuel occurs. According to step S03, the gas mixture exiting the oxidation zone is supplied to the injection and gas forming zone. Further, in step S04 additional fuel is supplied to the injection and gas forming zone. The mixture produced in the injection and mixture forming zone is then supplied in step S05 to the reforming zone, where it is reformed in step S06 within an endothermic reaction, utilizing the reaction heat of the exothermic oxidation. In step S07 the reformate is extracted. The features of the present invention disclosed in the preceding description, in the drawings and in the claims can be essential for the implementation of the invention, individually and in combination. Reference numerals: 12 fuel 14 fuel 16 oxidant 18 oxidant 2 0 oxidant 22 reformate 24 oxidation zone 26 reforming zone 2 8 heat 30 injection and mixture forming zone 34 gas mixture 36 cooling zone CLAIMS 1. A reformer for converting fuel (12) and oxidant (16, 18, 20) into reformate (22), comprising an oxidation zone (24) and a reforming zone (26), wherein a mixture of fuel (12) and oxidant (16, 18, 20) may be supplied to the oxidation zone (24), and the mixture may be supplied at least partially to the reforming zone upon an at least partial oxidation of the fuel (12) characterized in that fuel (14) may additionally be supplied to the reforming zone (26), and heat (28) may be supplied to the reforming zone (26). 2. The reformer according to claim 1, characterized in that heat (28) from the exothermic oxidation within the oxidation zone (24) may be supplied to the reforming zone (26) . 3. The reformer according to claim 1 or 2, characterized 4. in that the reforming zone (26) comprises an oxidation supply through which oxidant (16, 18, 20) may be supplied additionally. 5. The reformer according to one of the preceding claims, 6. characterized in that the additional fuel (14) may be supplied to an injection and mixture forming zone (30), and the additional fuel (14) can flow from the injection and mixture forming zone (30) into the reforming zone (26) . 5. The reformer according to one of the preceding claims, 6. characterized in that the additional fuel (14) is at least 7. partially evaporated by the thermal energy of the gas mixture (34) exiting the oxidation zone (24). 8. The reformer according to claim 4 or 5, characterized 9. in that, the gas mixture (34) generated in the oxidation 10. zone (24) may be partially supplied to the reforming zone 11. (26), bypassing the injection and mixture forming zone(30) . 12. A method for converting fuel (12) and oxidant (16, 18, 13. 20) into reformate (22) in a reformer having an oxidation 14. zone (24) and a reforming zone (26) , wherein a mixture of 15. fuel (12) and oxidant (16, 18, 20) is supplied to the oxidation zone (24), the mixture being supplied at least partially to the reforming zone (26) upon an at least partial 16. oxidation of the fuel (12) , characterized in that additional fuel (14) is supplied to the reforming zone (26), and heat (28) is supplied to the reforming zone (26). 8. The method according to claim 7, characterized in that heat (28) from the exothermic oxidation within the oxidation zone (24) is supplied to the reforming zone (26). 9. The method according to claim 7 or 8, characterized in 10. that the reforming zone (26) comprises an oxidant supply- 11. through which additional oxidant (16, 18, 20) is supplied. 12. The method according to one of claims■7 to 9, characterized in that the additional fuel (14) is supplied to an injection and mixture forming zone (30), and the additional fuel (14) flows from the injection and mixture forming zone (30) into the reforming zone (26) . 11. The method according to one of claims 7 to 10, characterized in that the additional fuel (14) is evaporated at least partially by the thermal energy of the gas mixture (34) exiting the oxidation zone (24). 12. The method according to claim 10 or 11, characterized in that the gas mixture (34) which is produced in the oxidation zone (24) is partially supplied to the reforming zone (26), bypassing the injection and mixture forming zone (30) . |
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2141-chenp-2006 abstract-duplicate.pdf
2141-chenp-2006 claims-duplicate.pdf
2141-CHENP-2006 CORRESPONDENCE OTHERS.pdf
2141-CHENP-2006 CORRESPONDENCE PO.pdf
2141-chenp-2006 description (complete)-duplicate.pdf
2141-chenp-2006 drawings-duplicate.pdf
2141-CHENP-2006 POWER OF ATTORNEY.pdf
2141-chenp-2006-correspondnece-others.pdf
2141-chenp-2006-description(complete).pdf
Patent Number | 231234 | |||||||||
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Indian Patent Application Number | 2141/CHENP/2006 | |||||||||
PG Journal Number | 13/2009 | |||||||||
Publication Date | 27-Mar-2009 | |||||||||
Grant Date | 04-Mar-2009 | |||||||||
Date of Filing | 16-Jun-2006 | |||||||||
Name of Patentee | ENERDAY GmbH | |||||||||
Applicant Address | Kraillinger Strasse 5, 82131 Stockdorf, | |||||||||
Inventors:
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PCT International Classification Number | C01B | |||||||||
PCT International Application Number | PCT/DE2004/002758 | |||||||||
PCT International Filing date | 2004-12-16 | |||||||||
PCT Conventions:
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