EP1836744A1 - Reformer für eine brennstoffzelle - Google Patents
Reformer für eine brennstoffzelleInfo
- Publication number
- EP1836744A1 EP1836744A1 EP05825900A EP05825900A EP1836744A1 EP 1836744 A1 EP1836744 A1 EP 1836744A1 EP 05825900 A EP05825900 A EP 05825900A EP 05825900 A EP05825900 A EP 05825900A EP 1836744 A1 EP1836744 A1 EP 1836744A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- chamber
- fuel cell
- reformer
- heat pipe
- heat
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B3/00—Hydrogen; Gaseous mixtures containing hydrogen; Separation of hydrogen from mixtures containing it; Purification of hydrogen
- C01B3/02—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen
- C01B3/32—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air
- C01B3/34—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air by reaction of hydrocarbons with gasifying agents
- C01B3/38—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air by reaction of hydrocarbons with gasifying agents using catalysts
- C01B3/386—Catalytic partial combustion
-
- 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
- H01M8/06—Combination of fuel cells with means for production of reactants or for treatment of residues
-
- 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
- H01M8/04—Auxiliary arrangements, e.g. for control of pressure or for circulation of fluids
-
- 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
- H01M8/04—Auxiliary arrangements, e.g. for control of pressure or for circulation of fluids
- H01M8/04007—Auxiliary arrangements, e.g. for control of pressure or for circulation of fluids related to heat exchange
- H01M8/04014—Heat exchange using gaseous fluids; Heat exchange by combustion of reactants
-
- 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
- H01M8/04—Auxiliary arrangements, e.g. for control of pressure or for circulation of fluids
- H01M8/04007—Auxiliary arrangements, e.g. for control of pressure or for circulation of fluids related to heat exchange
- H01M8/04059—Evaporative processes for the cooling of a fuel cell
-
- 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
- H01M8/06—Combination of fuel cells with means for production of reactants or for treatment of residues
- H01M8/0606—Combination of fuel cells with means for production of reactants or for treatment of residues with means for production of gaseous reactants
- H01M8/0612—Combination of fuel cells with means for production of reactants or for treatment of residues with means for production of gaseous reactants from carbon-containing material
- H01M8/0625—Combination of fuel cells with means for production of reactants or for treatment of residues with means for production of gaseous reactants from carbon-containing material in a modular combined reactor/fuel cell structure
- H01M8/0631—Reactor construction specially adapted for combination reactor/fuel cell
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B2203/00—Integrated processes for the production of hydrogen or synthesis gas
- C01B2203/02—Processes for making hydrogen or synthesis gas
- C01B2203/025—Processes for making hydrogen or synthesis gas containing a partial oxidation step
- C01B2203/0261—Processes for making hydrogen or synthesis gas containing a partial oxidation step containing a catalytic partial oxidation step [CPO]
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B2203/00—Integrated processes for the production of hydrogen or synthesis gas
- C01B2203/06—Integration with other chemical processes
- C01B2203/066—Integration with other chemical processes with fuel cells
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B2203/00—Integrated processes for the production of hydrogen or synthesis gas
- C01B2203/08—Methods of heating or cooling
- C01B2203/0872—Methods of cooling
- C01B2203/0883—Methods of cooling by indirect heat exchange
-
- 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
- H01M8/04—Auxiliary arrangements, e.g. for control of pressure or for circulation of fluids
- H01M8/04007—Auxiliary arrangements, e.g. for control of pressure or for circulation of fluids related to heat exchange
- H01M8/04029—Heat exchange using liquids
-
- 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
Definitions
- the invention relates to a reformer for a fuel cell having a chamber having a chamber inlet to the inlet of a Reaktandengasgemisches and a chamber outlet to the outlet of a reformed gas, wherein in the chamber a catalytically active medium is arranged.
- Generic reformers have numerous applications. In particular, they serve to supply a hydrogen-rich gas mixture to a fuel cell, from which electrical energy can then be generated on the basis of electrochemical processes.
- fuel cells are used for example in the automotive sector as additional energy sources, so-called APUs ("auxiliary power unit").
- the design of the reformers depends on numerous factors. In addition to the consideration of the properties of the reaction system, for example, economic aspects are of importance, in particular the integration of the reformer in its environment. The latter also concerns how the material and energy flows entering and leaving the reactor are treated. Depending on the application and the environment of the reformer thus different reforming methods are used, whereby different reformer designs are necessary.
- CPOX Catalytic Partial Oxidation
- Fuel-air mixture the reaction in the flow direction can be divided into two different zones. Upon entry into the catalytic Medium first strong exothermic oxidation reactions take place. Subsequently, the intermediates occurring are reformed in a subsequent region of the catalytically active medium.
- the reformation process is an endothermic reaction in which the temperatures drop sharply, resulting in losses of revenue.
- the net heat production in the reforming process of the catalytic partial oxidation in the inlet region of the reformer is so great that damage to the materials involved can occur there.
- the catalytically active medium can be deactivated or the support materials can be destroyed. Since the liberated heat of reaction from the oxidation zone can not be brought into the reforming zone, the control of the reforming process is problematic, so that in general a polytropic reaction can not be avoided, but which has a lower degree of conversion.
- the invention provides that the reformer has a heat pipe with an outer cylindrical tube wall and an inner cylindrical boundary wall, wherein the chamber between the outer tube wall and the inner boundary wall is arranged.
- the basic idea of the invention is to achieve both a radially and axially isothermal temperature distribution in the catalytically active medium with the aid of a heat pipe, which is characterized by rapid heat transport.
- the chamber inlet is arranged near a first axial end of a heat pipe and the chamber outlet near a second axial end of the heat pipe, so that a temperature compensation can take place over the largest possible axial region of the heat pipe. It is particularly preferred if the chamber between the chamber inlet and the chamber outlet is formed spirally. Due to the small cross-sectional area through which the temperature gradients in the radial direction are thus minimized.
- FIG. 1 shows a cross section through a reformer in a first embodiment of the invention
- Fig. 2 shows the axial temperature profile in the reformer in polytroper (dashed curve) and isothermal process control (solid curve), and
- Fig. 3 shows the fuel cell system with the reformer in a schematic representation.
- Fig. 1 shows a reformer 10 for a fuel cell system shown below, wherein the reformer 10 has a heat pipe 12 with an outer circular cylindrical tube wall 14 and an inner also circular cylindrical boundary wall 16. At a first axial end 18 of the heat pipe 12 there is a chamber inlet 20 through which a reactant gas mixture, consisting for example of air and vaporized fuel, may enter the reformer. At a second axial end 22 of the heat pipe 12, a chamber outlet 24 is arranged, via which reformed gas can leave the reformer 10. Outer tube wall 14 and inner boundary wall 16 bound a chamber 26 which extends between the chamber inlet 20 and the chamber outlet 24. The chamber 26 is formed in the embodiment shown here between the chamber inlet 20 and the chamber outlet 24 spirally.
- a channel 28 is milled in that in the inner cylindrical boundary wall 16, a channel 28 is milled.
- the dimension A of the channel in the radial direction of the heat pipe 12 is small compared to the radium R of the heat pipe 12.
- the temperature gradient in the radial direction in the chamber 26 is very small.
- a bed 30 is arranged from a catalytically active medium, wherein the catalytically active medium is present in the form of pellets in the embodiment shown here.
- the inner boundary wall 16 encloses an inner chamber 32 which has a filling of a liquid metal.
- Liquid metal fillings are particularly well suited for the temperature range up to 1100 ° C.
- lithium or sodium is used.
- the inner boundary wall 16 can be made of stainless steel.
- a heat exchanger 34 is arranged in the region of the second axial end 22 of the heat pipe 12.
- heat energy from the heat pipe 12 to other system components of the fuel cell can be transmitted.
- the heat energy can be transferred to a liquid or gaseous medium flowing in a pipeline 36 and from there to the other system components. Further details will be described below.
- FIG. 3 shows the integration of the reformer 10 into a fuel cell system 38.
- a fuel supply line 39 is connected to a media delivery device 40 which is connected to an evaporator 42.
- Fuel supply line 39 and an air supply line 46 are connected to a mixture forming device 44, which in turn is connected to the chamber inlet 20.
- Adjoining the chamber outlet 24 of the reformer 10 is a fuel cell stack 48 followed by a fuel cell stack 48.
- burner 50 is connected downstream.
- the fuel cell stack 48 is still provided with a Kathodenluftzu- line 52.
- Fuel is supplied to the evaporator 42 via the fuel supply line 39 by means of the media delivery device 40, where it is converted into a gaseous phase.
- the vaporized fuel then flows into the mixture forming device 44, into which air is supplied via the air supply line 46 and mixed with the evaporated fuel.
- the fuel-air mixture is then introduced via the chamber inlet 20 into the reformer 10 (FIG. 1).
- the fuel-air mixture now enters the bed 30 with the catalytically active medium. By means of the bed 30 with the catalytically active medium takes place, a conversion of the fuel-air mixture to intermediates, wherein the initially released heat of reaction from the oxidation reactions by means of the heat pipe 12 is transferred to the filling of the inner chamber 32.
- the heat of reaction released in the region of the first axial end 18 of the heat pipe 12 is then transferred via the filling of the inner chamber 32 to the region of the second axial end 22 of the heat pipe 12.
- a local overheating at the first axial end 18 of the heat pipe 12 is avoided, as is usual in polytroper reaction (see Fig. 2, dashed curve) and a practically constant temperature over the entire axial extent of the heat pipe 12 is reached (see FIG 2, solid curve).
- the intermediates formed in the region of the first axial end 18 of the heat pipe 12 are now transported in the channel 28 in the region of the second axial end 22 of the heat pipe 12, where a reforming of the intermediates takes place.
- FIG. 2 shows how local overheating at the first axial end 18 of the heat pipe 12 in the region of the chamber inlet 20, as occurs in the prior art polytropic reaction guide (see FIG. 2, dashed curve), is avoided, and FIG by the use of the heat pipe 12 a practically constant temperature profile over the entire axial extent of the heat pipe 12 between the chamber inlet 20 and chamber outlet 24 is achieved (see Fig. 2, solid curve).
- the maximum temperature T ma ⁇ which should not be exceeded in order not to reduce the lifetime of the catalytically active medium and the carrier materials is not exceeded in any area of the heat pipe 12. Local overheating is excluded.
- the reformed gas leaving the chamber outlet 24 is now supplied to the fuel cell stack 48 (see FIG. 3), in which the electrical energy is released in a known manner.
- the gases flowing out of the fuel cell stack 48 are now supplied to the afterburner 50, in which they are still used thermally.
- the fuel cell system 38 Since the fuel cell system 38 overall has a surplus of heat energy dependent on the mass flow of the reactant gas mixture at the chamber inlet 20, it can be used by the heat exchanger 34 for further system components of the fuel cell system 38.
- system components may be the mixture formation device 44 or the cathode air of the cathode air supply line 52 of the fuel cell stack 48.
- the pipe 36 of the heat exchanger 34 is then to be connected in a corresponding manner with the air supply line 46 or the cathode air supply line 52.
- the heat energy from the heat exchanger 34 may also be supplied directly to a heating system in a combined system for providing electrical energy and heat.
- the control of the conversion processes is considerably simplified and the modulability with regard to the media flows is increased.
- the yield of reformed gas increases significantly.
- the reaction can be further optimized. If two reformers 10 are interconnected in a suitable manner via pipelines and valves, an alternating use and regeneration operation of the two reformers can be realized: while one of the two reformers is being regenerated, the second reformer can provide reformed gases for operation of the fuel cell system 38 , After regeneration of the first reformer and after exhaustion of the second reformer is switched and the first reformer can generate reformed gases for the fuel cell system 38 again. For higher gas flow rates, several reformers 10 can be operated in parallel. This also allows the use of various fuels, which may be in both liquid and gaseous form.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Sustainable Energy (AREA)
- Sustainable Development (AREA)
- Manufacturing & Machinery (AREA)
- Electrochemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Combustion & Propulsion (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Inorganic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Fuel Cell (AREA)
- Hydrogen, Water And Hydrids (AREA)
- Devices And Processes Conducted In The Presence Of Fluids And Solid Particles (AREA)
Abstract
Description
Claims
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102004063151A DE102004063151A1 (de) | 2004-12-22 | 2004-12-22 | Reformer für eine Brennstoffzelle |
PCT/DE2005/002242 WO2006066545A1 (de) | 2004-12-22 | 2005-12-12 | Reformer für eine brennstoffzelle |
Publications (1)
Publication Number | Publication Date |
---|---|
EP1836744A1 true EP1836744A1 (de) | 2007-09-26 |
Family
ID=36032126
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP05825900A Withdrawn EP1836744A1 (de) | 2004-12-22 | 2005-12-12 | Reformer für eine brennstoffzelle |
Country Status (9)
Country | Link |
---|---|
US (1) | US20090253005A1 (de) |
EP (1) | EP1836744A1 (de) |
JP (1) | JP2008524817A (de) |
KR (1) | KR20070086973A (de) |
CN (1) | CN101088188A (de) |
CA (1) | CA2589785A1 (de) |
DE (1) | DE102004063151A1 (de) |
EA (1) | EA010329B1 (de) |
WO (1) | WO2006066545A1 (de) |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102006039527A1 (de) * | 2006-08-23 | 2008-02-28 | Enerday Gmbh | Brennstoffzellensystem und Verfahren zum Betreiben eines Brennstoffzellensystems |
DE102006051740B4 (de) * | 2006-11-02 | 2012-03-08 | Enerday Gmbh | Verfahren zum Regenerieren eines Reformers und Klimaanlage |
DE102006051741B4 (de) * | 2006-11-02 | 2010-05-06 | Enerday Gmbh | Verfahren zum Regenerieren eines Reformers |
DE102006051748A1 (de) * | 2006-11-02 | 2008-05-08 | Enerday Gmbh | Verfahren zum Regenerieren eines Reformers |
EP2223371A1 (de) * | 2007-12-17 | 2010-09-01 | Shell Internationale Research Maatschappij B.V. | Auf brennstoffzelle basierendes verfahren zur stromerzeugung |
JP5820873B2 (ja) * | 2010-04-09 | 2015-11-24 | フラウンホーファー・ゲゼルシャフト・ツール・フェルデルング・デア・アンゲヴァンテン・フォルシュング・エー・ファウ | 高温燃料電池を有するシステム |
EP2681792B1 (de) * | 2011-02-28 | 2020-11-18 | Nicolas Kernene | Energieeinheit mit sicherer und stabiler wasserstoffspeicherung |
CN104203397A (zh) * | 2011-12-06 | 2014-12-10 | Hy9公司 | 催化剂容纳反应器***以及相关方法 |
EP2797150B1 (de) * | 2011-12-23 | 2017-11-15 | Posco Energy Co. Ltd. | Verdampfungs-wärmetauscher für eine brennstoffzelle |
KR101509021B1 (ko) | 2013-04-01 | 2015-04-07 | 주식회사 싸이텍 | 합성가스 대량생산을 위한 개질장치 |
JP6169939B2 (ja) * | 2013-10-08 | 2017-07-26 | 京セラ株式会社 | 燃料電池装置 |
US9145299B2 (en) | 2013-12-13 | 2015-09-29 | King Fahd University Of Petroleum And Minerals | Steam methane reforming reactor of shell and tube type with cylindrical slots |
US11667728B1 (en) | 2022-03-02 | 2023-06-06 | David T. Camp | Reactor and processes for endothermic reactions at high temperatures |
Family Cites Families (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS52129705A (en) * | 1976-04-24 | 1977-10-31 | Nissan Motor Co Ltd | Methanol-reforming apparatus |
US4315893A (en) * | 1980-12-17 | 1982-02-16 | Foster Wheeler Energy Corporation | Reformer employing finned heat pipes |
JPS63162503A (ja) * | 1986-12-25 | 1988-07-06 | Toyo Eng Corp | ガスの製造装置 |
FR2633635B1 (fr) * | 1988-06-29 | 1993-05-07 | Inst Francais Du Petrole | Procede de reformage catalytique avec circulation d'un fluide caloporteur dans une pluralite d'espaces internes creux |
JPH02124701A (ja) * | 1988-11-01 | 1990-05-14 | Toshiba Corp | 多管式改質装置 |
JP2601707B2 (ja) * | 1988-12-13 | 1997-04-16 | 東洋エンジニアリング株式会社 | 触媒反応装置 |
ATE105854T1 (de) * | 1989-06-30 | 1994-06-15 | Inst Francais Du Petrole | Katalytisches reformierungsverfahren mit zirkulation von wärmeübertragungsmittel in ein vielfaches von inneren aushöhlungen. |
JPH03232703A (ja) * | 1989-12-26 | 1991-10-16 | Tokyo Electric Power Co Inc:The | 炭化水素の改質装置 |
CN2077087U (zh) * | 1990-08-03 | 1991-05-15 | 中国石油化工总公司湖北化肥厂 | 大型氨厂转化炉燃烧空气节能装置 |
JP3066244B2 (ja) * | 1994-04-28 | 2000-07-17 | 三洋電機株式会社 | ガス改質装置及びガス改質方法 |
US5763114A (en) * | 1994-09-01 | 1998-06-09 | Gas Research Institute | Integrated reformer/CPN SOFC stack module design |
AU3277097A (en) * | 1996-06-28 | 1998-01-21 | Matsushita Electric Works Ltd. | Modification apparatus |
DE19716470C1 (de) * | 1997-04-19 | 1998-10-01 | Mtu Friedrichshafen Gmbh | Integriertes Brennstoffaufbereitungsmodul für eine Brennstoffzellenanlage |
CA2335483C (en) * | 1999-04-20 | 2005-03-29 | Tokyo Gas Co., Ltd. | Single-pipe cylindrical reformer and operation method therefor |
CA2357960C (en) * | 2000-10-10 | 2007-01-30 | Tokyo Gas Co., Ltd. | Single-pipe cylinder type reformer |
EP1453599A4 (de) * | 2001-08-11 | 2006-05-17 | Texaco Development Corp | Kraftstoffprozessor mit heat-pipe-kühlung |
DE50305340D1 (de) * | 2002-03-25 | 2006-11-23 | Viessmann Werke Kg | Vorrichtung zur erzeugung von wasserstoff |
-
2004
- 2004-12-22 DE DE102004063151A patent/DE102004063151A1/de not_active Withdrawn
-
2005
- 2005-12-12 JP JP2007547163A patent/JP2008524817A/ja not_active Withdrawn
- 2005-12-12 EA EA200701352A patent/EA010329B1/ru not_active IP Right Cessation
- 2005-12-12 EP EP05825900A patent/EP1836744A1/de not_active Withdrawn
- 2005-12-12 US US11/721,748 patent/US20090253005A1/en not_active Abandoned
- 2005-12-12 CA CA002589785A patent/CA2589785A1/en not_active Abandoned
- 2005-12-12 KR KR1020077015549A patent/KR20070086973A/ko not_active Application Discontinuation
- 2005-12-12 CN CNA2005800442839A patent/CN101088188A/zh active Pending
- 2005-12-12 WO PCT/DE2005/002242 patent/WO2006066545A1/de active Application Filing
Non-Patent Citations (1)
Title |
---|
See references of WO2006066545A1 * |
Also Published As
Publication number | Publication date |
---|---|
JP2008524817A (ja) | 2008-07-10 |
US20090253005A1 (en) | 2009-10-08 |
WO2006066545A1 (de) | 2006-06-29 |
DE102004063151A1 (de) | 2006-07-06 |
CN101088188A (zh) | 2007-12-12 |
WO2006066545A8 (de) | 2007-08-09 |
EA010329B1 (ru) | 2008-08-29 |
KR20070086973A (ko) | 2007-08-27 |
EA200701352A1 (ru) | 2007-10-26 |
CA2589785A1 (en) | 2006-06-29 |
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Legal Events
Date | Code | Title | Description |
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