WO2010142533A1 - System for converting fuel material - Google Patents

System for converting fuel material Download PDF

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Publication number
WO2010142533A1
WO2010142533A1 PCT/EP2010/057300 EP2010057300W WO2010142533A1 WO 2010142533 A1 WO2010142533 A1 WO 2010142533A1 EP 2010057300 W EP2010057300 W EP 2010057300W WO 2010142533 A1 WO2010142533 A1 WO 2010142533A1
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WO
WIPO (PCT)
Prior art keywords
ash
separator
fuel
reactor
carbon
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.)
Ceased
Application number
PCT/EP2010/057300
Other languages
French (fr)
Inventor
Michel Vandycke
Laurent Maghdissian
Corinne Beal
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
GE Vernova GmbH
Original Assignee
Alstom Technology AG
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Alstom Technology AG filed Critical Alstom Technology AG
Priority to JP2012514413A priority Critical patent/JP5496327B2/en
Priority to US13/375,977 priority patent/US8807054B2/en
Priority to CN201080026196.1A priority patent/CN102460017B/en
Priority to CA2763964A priority patent/CA2763964C/en
Priority to AU2010257649A priority patent/AU2010257649B2/en
Publication of WO2010142533A1 publication Critical patent/WO2010142533A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
    • F23C—METHODS OR APPARATUS FOR COMBUSTION USING FLUID FUEL OR SOLID FUEL SUSPENDED IN  A CARRIER GAS OR AIR 
    • F23C10/00—Fluidised bed combustion apparatus
    • F23C10/002—Fluidised bed combustion apparatus for pulverulent solid fuel
    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
    • F23C—METHODS OR APPARATUS FOR COMBUSTION USING FLUID FUEL OR SOLID FUEL SUSPENDED IN  A CARRIER GAS OR AIR 
    • F23C10/00—Fluidised bed combustion apparatus
    • F23C10/005—Fluidised bed combustion apparatus comprising two or more beds
    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
    • F23J—REMOVAL OR TREATMENT OF COMBUSTION PRODUCTS OR COMBUSTION RESIDUES; FLUES 
    • F23J1/00—Removing ash, clinker, or slag from combustion chambers
    • F23J1/02—Apparatus for removing ash, clinker, or slag from ash-pits, e.g. by employing trucks or conveyors, by employing suction devices
    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
    • F23C—METHODS OR APPARATUS FOR COMBUSTION USING FLUID FUEL OR SOLID FUEL SUSPENDED IN  A CARRIER GAS OR AIR 
    • F23C2900/00—Special features of, or arrangements for combustion apparatus using fluid fuels or solid fuels suspended in air; Combustion processes therefor
    • F23C2900/99008—Unmixed combustion, i.e. without direct mixing of oxygen gas and fuel, but using the oxygen from a metal oxide, e.g. FeO
    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
    • F23J—REMOVAL OR TREATMENT OF COMBUSTION PRODUCTS OR COMBUSTION RESIDUES; FLUES 
    • F23J2700/00—Ash removal, handling and treatment means; Ash and slag handling in pulverulent fuel furnaces; Ash removal means for incinerators
    • F23J2700/002—Ash and slag handling in pulverulent fuel furnaces
    • 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
    • Y02E20/00—Combustion technologies with mitigation potential
    • Y02E20/34—Indirect CO2mitigation, i.e. by acting on non CO2directly related matters of the process, e.g. pre-heating or heat recovery

Definitions

  • the present invention is related to a system for converting fuel material, such as a boiler, and is more particularly directed to an oxidation-reduction reactor system used in fuel conversion.
  • the current ratio between fly ash and bottom ash is 60/40 and tends to go down to 40/60.
  • a dedicated bottom ash extraction system has to be designed to remove approximately half of the ash introduced via the fuel material into the system.
  • a major challenge is to separate the fuel particles and the ash from the oxygen carrier before sending the oxygen carrier to the air reactor for oxidation and regeneration.
  • the conventional chemical looping systems for converting fuel material comprise a carbon separator, as mentioned for instance in document FR 2 850 156.
  • the carbon separator which is also called “carbon stripper”
  • the conventional chemical looping systems also comprise an ash separator placed at the bottom of the fuel and/or air reactor in order to drain ash from the system. This extraction is typically located at the very bottom of the reactor.
  • the hole can be located in the middle of the grate of the reactor by removing some nozzle which leads to a vertical extraction.
  • the hole can be located on a side wall of the reactor with a lateral extraction with a flow that is controlled by a cone valve.
  • the solids mixture at the bottom of fuel and air reactors typically comprises about 10% ash. If lkg/s ash is to be extracted, this would mean that 10 kg/s of the mixture containing lkg/s ash will be extracted. Thus, the solid quantity that would be needed to treat is ten times higher than the really needed solid quantity.
  • an object of the present invention is to provide a system for converting fuel material in such a manner as to solve the above- described problems.
  • a carbon separator that receives fuel particles, ash and oxide particles produced in the first reactor and suitable for separating the oxide particles and ash from the fuel particles, the carbon separator comprising an outlet path for the oxide particles and ash exhaust.
  • said outlet path of the carbon separator is connected to an ash separator for separating the ash from the oxide particles.
  • This specific arrangement provides that starting from a mixture of fuel particles, ash and oxide particles, it is possible to separate theses three compounds from each other in a simple way.
  • the device made of the carbon separator and the ash separator is compact and economic to install.
  • both of the carbon separator and the ash separator are fluidized and that the system comprises means for controlling the fluidization velocity of each separator.
  • the ash density being higher than the fuel particles density
  • the fluidization velocity of the ash separator is preferably higher than the fluidization velocity of the carbon separator.
  • the carbon separator and the ash separator can be adjacent separators via a common side wall .
  • the carbon separator and the ash separator can be connected by a pipe.
  • the ash separator can be placed below the carbon separator.
  • the fuel reactor is advantageously connected to a low efficiency cyclone separator comprising a lower outlet connected to the carbon separator and an upper outlet connected to a high efficiency cyclone separator.
  • the fuel material is typically coal.
  • - Figure 2 is a schematic view of a part of the system according to a first embodiment
  • - Figure 3 a schematic view of a part of the system according to a second embodiment.
  • the solid fuel material is preferably coal.
  • the metal oxide can be based on iron, nickel, alumina or a mixture thereof.
  • the fuel reactor 2 is fluidized by steam and/or recycled flue gas and/or carbon dioxide.
  • a first separation device, preferably a low efficiency separation cyclone 7, is fed with combustion gases, ash, fuel particles and oxide particles coming from the fuel reactor 2.
  • the combustion gases comprise mainly CO 2 and steam.
  • the upper stream of the solids of the low efficiency separation cyclone 7 is circulated into a high separation device, preferably a high efficiency separation cyclone 8.
  • a high separation device preferably a high efficiency separation cyclone 8.
  • the carbon separator 4 separates out the fine and light particles, such as the carbon-containing residue, which are sent to the fuel reactor 2, from the denser and larger oxide particles and ash which are sent to the air reactor 3.
  • the carbon separator 4 is connected to an ash separator 10 that includes a specific vent 10a to allow the ash to escape.
  • the average particle diameter of the fuel material entering the fuel reactor 2 is preferably less than the average particle diameter of the oxide material. More preferably, the average particle diameter of the fuel material is controlled to be at least twice smaller than the average particle diameter of the oxide material.
  • the average particle diameter of the fuel material can be equal to about 50 ⁇ m. It can be comprised between 50 and 60 ⁇ m. In this case, the density of the oxide particles is higher than the density of the fuel particles, the density of the ash being comprised between the density of the fuel particles and the density of the oxide particles.
  • FIG. 4 A detailed view of the association of the carbon separator 4 and the ash separator 10 is shown in figures 2 and 3.
  • Figures 2 and 3 schematically illustrate two embodiments of an assembly of a carbon separator and an ash separator used in the system for converting fuel material according to the invention.
  • the carbon separator 4 comprises an inlet 4a through which the fuel particles FP, the oxide particles OP and the ash A enter the carbon separator 4.
  • the oxide particles OP are oxide particles that have been at least partially reduced in the fuel reactor.
  • the carbon separator 4 is fluidized by fluidization means F.
  • the fluidization means F can be steam and/or recycled flue gas and/or CO 2 inlets placed at the bottom of the carbon separator 4.
  • the fine and light fuel particles FP having a density of about 1.2 are directed toward the fuel reactor via outlets 4b of the carbon separator 4 while the denser and larger oxide particles OP and ash A are routed towards the ash separator 10.
  • the ash separator 10 is fluidized by fluidization means F.
  • the fluidization means F can be steam and/or recycled flue gas and/or CO 2 inlets placed at the bottom of the carbon separator 4.
  • the light ash A flows out the vent 10a towards a gas treatment system while the denser oxide particles OP passes through an outlet 10b of the ash separator 10 towards the air reactor.
  • the fluidizing velocity of the carbon separator 4 and of the ash separator 10 can be controlled in order to control the ash concentration in the system.
  • the fluidizing velocity can be based on the respective density of ash A and oxide particles OP (about 2.5 and 4.5 respectively).
  • the ash separator 10 can be fluidized at a velocity comprised between 0.3 and 0.8 m/s and the carbon separator 4 can be fluidized at a velocity comprised between 0.1 and 0.6 m/s.
  • the carbon separator 4 and the ash separator 10 are adjacent via a common side wall 13.
  • the carbon separator 4 and the ash separator 10 are connected by an opening 4c of the side wall 13.
  • the carbon separator 4 and the ash separator 10 are connected by a pipe 4c. Moreover, the ash separator 10 can be placed below the carbon separator 4 in order to facilitate the passage of the oxide particles OP and the ash A from the carbon separator 4 to the ash separator 10.

Landscapes

  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • General Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Combustion & Propulsion (AREA)
  • Fluidized-Bed Combustion And Resonant Combustion (AREA)
  • Devices And Processes Conducted In The Presence Of Fluids And Solid Particles (AREA)
  • Combined Means For Separation Of Solids (AREA)
  • Gasification And Melting Of Waste (AREA)

Abstract

The invention is related to a system (1) for converting fuel material comprising : a first reactor (2) in which a fuel material reacts with an oxide material for producing reaction products including fuel particles, ash and oxide particles, a second reactor (3) for oxidizing the oxide particles produced in the first reactor (2), a carbon separator (4) that receives fuel particles, ash and oxide particles produced in the first reactor (2) and suitable for separating the oxide particles and ash from the fuel particles, the carbon separator (4) comprising an outlet path (4c) for the oxide particles and ash exhaust, characterized in that said outlet path (4c) of the carbon separator (4) is connected to an ash separator (10) for separating the ash from the oxide particles.

Description

SYSTEM FOR CONVERTING FUEL MATERIAL
The present invention is related to a system for converting fuel material, such as a boiler, and is more particularly directed to an oxidation-reduction reactor system used in fuel conversion.
Chemical looping technology is a promising technology intended to achieve gasification or combustion of solid fuels replacing direct oxygen feed by using an oxygen carrier. Chemical looping is a process by which combustion or gasification of a carbon-based fuel occurs in two steps. In a first step, the oxygen carrier delivers oxygen in a fuel reactor where the oxygen carrier is reduced by the solid fuel and is then transferred to an air reactor. Fuel particles, ash and reduced oxygen carrier are produced in the fuel reactor. In a second step, the reduced oxygen carrier is oxidized by air in the air reactor. In the chemical looping process, the gas resulting from the combustion or gasification of the fuel in the fuel reactor is then free or nearly free from nitrogen. The oxygen carrier can typically comprise a metal oxide or other oxygen rich compounds. Most of chemical looping technologies use the fluidized beds technology for the fuel reactor to benefit from the high residence time as well as from the good mixing associated with fluidized beds. Fluidized beds can be bubbling fluidized beds or circulating fluidized beds.
Typical crushed coal that is introduced into conventional systems for converting fuel material has a mean diameter of 2 mm and the top size of the coal can reach 20 mm. The biggest particles that do not end as fly ash have hence to be removed as bottom ash.
The current ratio between fly ash and bottom ash is 60/40 and tends to go down to 40/60. A dedicated bottom ash extraction system has to be designed to remove approximately half of the ash introduced via the fuel material into the system.
Thus, a major challenge is to separate the fuel particles and the ash from the oxygen carrier before sending the oxygen carrier to the air reactor for oxidation and regeneration.
The conventional chemical looping systems for converting fuel material comprise a carbon separator, as mentioned for instance in document FR 2 850 156. The carbon separator, which is also called "carbon stripper", is placed between the air reactor and the fuel reactor. The conventional chemical looping systems also comprise an ash separator placed at the bottom of the fuel and/or air reactor in order to drain ash from the system. This extraction is typically located at the very bottom of the reactor. Several designs exist with different locations for the extraction hole. The hole can be located in the middle of the grate of the reactor by removing some nozzle which leads to a vertical extraction. The hole can be located on a side wall of the reactor with a lateral extraction with a flow that is controlled by a cone valve.
These systems suffer the shortcoming that the ash separator involves a heavy and complex separator system at the bottom or nearly the bottom of the fuel and/or air reactor.
Moreover, the solids mixture at the bottom of fuel and air reactors typically comprises about 10% ash. If lkg/s ash is to be extracted, this would mean that 10 kg/s of the mixture containing lkg/s ash will be extracted. Thus, the solid quantity that would be needed to treat is ten times higher than the really needed solid quantity.
Thus, an object of the present invention is to provide a system for converting fuel material in such a manner as to solve the above- described problems.
The object mentioned above is accomplished by a system for converting fuel material comprising : - a first reactor in which a fuel material reacts with an oxide material for producing reaction products including fuel particles, ash and oxide particles,
- a second reactor for oxidizing the oxide particles produced in the first reactor,
- a carbon separator that receives fuel particles, ash and oxide particles produced in the first reactor and suitable for separating the oxide particles and ash from the fuel particles, the carbon separator comprising an outlet path for the oxide particles and ash exhaust. According to the present invention, said outlet path of the carbon separator is connected to an ash separator for separating the ash from the oxide particles.
This specific arrangement provides that starting from a mixture of fuel particles, ash and oxide particles, it is possible to separate theses three compounds from each other in a simple way. The device made of the carbon separator and the ash separator is compact and economic to install.
Thus, oxide particles can be sent to the air reactor to be regenerated. The unburned carbon can be sent back to the fuel reactor for further oxidation and the ash is removed which avoids an ash enrichment in the system that could cause an agglomeration.
Last, this specific arrangement avoids a complex and expensive use of an ash separator at the bottom of the fuel and/or air reactor.
It is to be appreciated that both of the carbon separator and the ash separator are fluidized and that the system comprises means for controlling the fluidization velocity of each separator.
The ash density being higher than the fuel particles density, the fluidization velocity of the ash separator is preferably higher than the fluidization velocity of the carbon separator. The carbon separator and the ash separator can be adjacent separators via a common side wall .
The carbon separator and the ash separator can be connected by a pipe. In this case, the ash separator can be placed below the carbon separator.
The fuel reactor is advantageously connected to a low efficiency cyclone separator comprising a lower outlet connected to the carbon separator and an upper outlet connected to a high efficiency cyclone separator. The fuel material is typically coal.
The oxide material is typically metal oxide.
Other features and advantages of the invention will become apparent from the following description of embodiments of the invention given by way of non-limiting examples only, and with reference to the accompanying drawings, in which :
- Figure 1 is a schematic diagram of a system for converting fuel material according to the invention,
- Figure 2 is a schematic view of a part of the system according to a first embodiment, and - Figure 3 a schematic view of a part of the system according to a second embodiment.
As illustrated in figure 1, a system 1 for converting fuel material according to the invention, which is intended to produce electricity and/or steam, comprises a fuel reactor 2, an air reactor 3 and a carbon separator 4.
A solid fuel material coming from a fuel silo 5 and a metal oxide coming from an oxide silo 6 enter the fuel reactor 2. The solid fuel material is preferably coal. The metal oxide can be based on iron, nickel, alumina or a mixture thereof. The fuel reactor 2 is fluidized by steam and/or recycled flue gas and/or carbon dioxide. A first separation device, preferably a low efficiency separation cyclone 7, is fed with combustion gases, ash, fuel particles and oxide particles coming from the fuel reactor 2. The combustion gases comprise mainly CO2 and steam.
The efficiency of a separation device is the ratio of the quantity of particles collected by the device to the quantity of solids at the inlet of the device.
The upper stream of the solids of the low efficiency separation cyclone 7 is circulated into a high separation device, preferably a high efficiency separation cyclone 8. Thus, the solids comprising mainly fine carbon particles are separated from the fly ash and are re-introduced in the fuel reactor 2 via a seal pot 14.
The solids leaving the low efficiency cyclone 7 enter a seal pot 9 from which a first portion is routed into the fuel reactor 2 and from which a second portion is routed into the carbon separator 4. The seal pot 9 can be fluidized by steam and/or recycled flue gas.
The carbon separator 4 separates out the fine and light particles, such as the carbon-containing residue, which are sent to the fuel reactor 2, from the denser and larger oxide particles and ash which are sent to the air reactor 3. According to the invention, the carbon separator 4 is connected to an ash separator 10 that includes a specific vent 10a to allow the ash to escape. The average particle diameter of the fuel material entering the fuel reactor 2 is preferably less than the average particle diameter of the oxide material. More preferably, the average particle diameter of the fuel material is controlled to be at least twice smaller than the average particle diameter of the oxide material. The average particle diameter of the fuel material can be equal to about 50 μm. It can be comprised between 50 and 60 μm. In this case, the density of the oxide particles is higher than the density of the fuel particles, the density of the ash being comprised between the density of the fuel particles and the density of the oxide particles. The oxide particles coming from the carbon and ash separator
4,10 are oxidized by air in the air reactor 3. The oxides and the depleted air leaving the air reactor 3 enter a separation device 11, typically a cyclone separator, in which the oxide particles are separated from the gases comprising N2 and O2. The solid oxide particles extracted from the bottom of the cyclone 11 enter a seal pot 12 from which a first portion is transferred to the bottom of the air reactor 3 and from which a second portion is routed to the bottom of the fuel reactor 2. The seal pot 12 can be fluidized with air. A detailed view of the association of the carbon separator 4 and the ash separator 10 is shown in figures 2 and 3. Figures 2 and 3 schematically illustrate two embodiments of an assembly of a carbon separator and an ash separator used in the system for converting fuel material according to the invention. The carbon separator 4 comprises an inlet 4a through which the fuel particles FP, the oxide particles OP and the ash A enter the carbon separator 4. The oxide particles OP are oxide particles that have been at least partially reduced in the fuel reactor. The carbon separator 4 is fluidized by fluidization means F. The fluidization means F can be steam and/or recycled flue gas and/or CO2 inlets placed at the bottom of the carbon separator 4.
The fine and light fuel particles FP having a density of about 1.2 are directed toward the fuel reactor via outlets 4b of the carbon separator 4 while the denser and larger oxide particles OP and ash A are routed towards the ash separator 10. The ash separator 10 is fluidized by fluidization means F. The fluidization means F can be steam and/or recycled flue gas and/or CO2 inlets placed at the bottom of the carbon separator 4. The light ash A flows out the vent 10a towards a gas treatment system while the denser oxide particles OP passe through an outlet 10b of the ash separator 10 towards the air reactor.
The fluidizing velocity of the carbon separator 4 and of the ash separator 10 can be controlled in order to control the ash concentration in the system. The fluidizing velocity can be based on the respective density of ash A and oxide particles OP (about 2.5 and 4.5 respectively). Thus, the ash separator 10 can be fluidized at a velocity comprised between 0.3 and 0.8 m/s and the carbon separator 4 can be fluidized at a velocity comprised between 0.1 and 0.6 m/s.
According to a first embodiment, as shown in figure 2, the carbon separator 4 and the ash separator 10 are adjacent via a common side wall 13. The carbon separator 4 and the ash separator 10 are connected by an opening 4c of the side wall 13.
According to a second embodiment, as shown in figure 3, the carbon separator 4 and the ash separator 10 are connected by a pipe 4c. Moreover, the ash separator 10 can be placed below the carbon separator 4 in order to facilitate the passage of the oxide particles OP and the ash A from the carbon separator 4 to the ash separator 10.

Claims

1. A system (1) for converting fuel material comprising :
- a first reactor (2) in which a fuel material reacts with an oxide material for producing reaction products including fuel particles, ash and oxide particles,
- a second reactor (3) for oxidizing the oxide particles produced in the first reactor (2),
- a carbon separator (4) that receives fuel particles, ash and oxide particles produced in the first reactor (2) and suitable for separating the oxide particles and ash from the fuel particles, the carbon separator (4) comprising an outlet path (4c) for the oxide particles and ash exhaust,
characterized in that said outlet path (4c) of the carbon separator (4) is connected to an ash separator (10) for separating the ash from the oxide particles.
2. A system (1) according to claim 1, characterized in that both of the carbon separator (4) and the ash separator (10) are fluidized and in that the system (1) comprises means for controlling the fluidization velocity of each separator (4,10).
3. A system (1) according to claim 2, characterized in that the fluidization velocity of the ash separator (10) is higher than the fluidization velocity of the carbon separator (4).
4. A system (1) according to any one of claims 1 to 3, characterized in that the carbon separator (4) and the ash separator (10) are adjacent separators (4,10) via a common side wall (13).
5. A system (1) according to any one of claims 1 to 3, characterized in that the carbon separator (4) and the ash separator (10) are connected by a pipe (4c).
6. A system (1) according to claim 5, characterized in that the ash separator (10) is placed below the carbon separator (4).
7. A system (1) according to any one of claims 1 to 6, characterized in that the fuel reactor (2) is connected to a low efficiency cyclone separator (7) comprising a lower outlet connected to the carbon separator (4) and an upper outlet connected to a high efficiency cyclone separator (8).
8. A system (1) according to any one of claims 1 to 7, characterized in that the fuel material is coal.
9. A system (1) according to any one of claims 1 to 8, characterized in that the oxide material is metal oxide.
PCT/EP2010/057300 2009-06-12 2010-05-27 System for converting fuel material Ceased WO2010142533A1 (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
JP2012514413A JP5496327B2 (en) 2009-06-12 2010-05-27 Fuel material conversion system
US13/375,977 US8807054B2 (en) 2009-06-12 2010-05-27 System for converting fuel materials
CN201080026196.1A CN102460017B (en) 2009-06-12 2010-05-27 System for converting fuel material
CA2763964A CA2763964C (en) 2009-06-12 2010-05-27 System for converting fuel material
AU2010257649A AU2010257649B2 (en) 2009-06-12 2010-05-27 System for converting fuel material

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP09162600.2 2009-06-12
EP09162600.2A EP2273192B1 (en) 2009-06-12 2009-06-12 System for converting fuel material

Publications (1)

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WO2010142533A1 true WO2010142533A1 (en) 2010-12-16

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US (1) US8807054B2 (en)
EP (1) EP2273192B1 (en)
JP (1) JP5496327B2 (en)
CN (1) CN102460017B (en)
AU (1) AU2010257649B2 (en)
CA (1) CA2763964C (en)
ES (1) ES2421210T3 (en)
PL (1) PL2273192T3 (en)
WO (1) WO2010142533A1 (en)

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