WO2012034141A1 - Fluidised bed pyrolysis apparatus and method - Google Patents

Fluidised bed pyrolysis apparatus and method Download PDF

Info

Publication number
WO2012034141A1
WO2012034141A1 PCT/ZA2011/000067 ZA2011000067W WO2012034141A1 WO 2012034141 A1 WO2012034141 A1 WO 2012034141A1 ZA 2011000067 W ZA2011000067 W ZA 2011000067W WO 2012034141 A1 WO2012034141 A1 WO 2012034141A1
Authority
WO
WIPO (PCT)
Prior art keywords
pyrolysis
combustion
zone
fluidised
particles
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/ZA2011/000067
Other languages
French (fr)
Other versions
WO2012034141A4 (en
Inventor
Michael David Heydenrych
Stephen David Swart
Akwasi Acheampong Boateng
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.)
University of Pretoria
Original Assignee
University of Pretoria
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 University of Pretoria filed Critical University of Pretoria
Priority to US13/820,721 priority Critical patent/US9580657B2/en
Priority to BR112013005718A priority patent/BR112013005718B1/en
Priority to EP11782355.9A priority patent/EP2614128B1/en
Priority to CA2810724A priority patent/CA2810724C/en
Priority to CN201180049338.0A priority patent/CN103180412B/en
Publication of WO2012034141A1 publication Critical patent/WO2012034141A1/en
Publication of WO2012034141A4 publication Critical patent/WO2012034141A4/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10B—DESTRUCTIVE DISTILLATION OF CARBONACEOUS MATERIALS FOR PRODUCTION OF GAS, COKE, TAR, OR SIMILAR MATERIALS
    • C10B49/00—Destructive distillation of solid carbonaceous materials by direct heating with heat-carrying agents including the partial combustion of the solid material to be treated
    • C10B49/16—Destructive distillation of solid carbonaceous materials by direct heating with heat-carrying agents including the partial combustion of the solid material to be treated with moving solid heat-carriers in divided form
    • C10B49/20—Destructive distillation of solid carbonaceous materials by direct heating with heat-carrying agents including the partial combustion of the solid material to be treated with moving solid heat-carriers in divided form in dispersed form
    • C10B49/22—Destructive distillation of solid carbonaceous materials by direct heating with heat-carrying agents including the partial combustion of the solid material to be treated with moving solid heat-carriers in divided form in dispersed form according to the "fluidised bed" technique
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10B—DESTRUCTIVE DISTILLATION OF CARBONACEOUS MATERIALS FOR PRODUCTION OF GAS, COKE, TAR, OR SIMILAR MATERIALS
    • C10B53/00—Destructive distillation, specially adapted for particular solid raw materials or solid raw materials in special form
    • C10B53/02—Destructive distillation, specially adapted for particular solid raw materials or solid raw materials in special form of cellulose-containing material
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10K—PURIFYING OR MODIFYING THE CHEMICAL COMPOSITION OF COMBUSTIBLE GASES CONTAINING CARBON MONOXIDE
    • C10K1/00—Purifying combustible gases containing carbon monoxide
    • C10K1/08—Purifying combustible gases containing carbon monoxide by washing with liquids; Reviving the used wash liquors
    • C10K1/16—Purifying combustible gases containing carbon monoxide by washing with liquids; Reviving the used wash liquors with non-aqueous liquids
    • 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
    • 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
    • F23C10/01—Fluidised bed combustion apparatus in a fluidised bed of catalytic particles
    • 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
    • F23C10/18—Details; Accessories
    • F23C10/20—Inlets for fluidisation air, e.g. grids; Bottoms
    • 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
    • F23C10/18—Details; Accessories
    • F23C10/24—Devices for removal of material from the bed
    • 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
    • Y02E50/00—Technologies for the production of fuel of non-fossil origin
    • Y02E50/10—Biofuels, e.g. bio-diesel
    • 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
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00—Technologies relating to chemical industry
    • Y02P20/10—Process efficiency
    • Y02P20/129—Energy recovery, e.g. by cogeneration, H2recovery or pressure recovery turbines
    • 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
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00—Technologies relating to chemical industry
    • Y02P20/141—Feedstock
    • Y02P20/145—Feedstock the feedstock being materials of biological origin

Definitions

  • the invention relates to the pyroiysis of carbonaceous material, such as bio-mass, in a fluidised bed pyroiysis apparatus.
  • Fast pyroiysis of bio-mass involves rapidly heating solid bio-mass to a temperature of 400°C to 600°C in reducing conditions so that it forms an oil. This is typically done in a fluidized bed, where approximately 60% of the original biomass can be recovered as oil.
  • the pyroiysis is endothermic in nature, and the energy required is typically obtained by heating the fluidized bed indirectly, using electrical heating elements.
  • the source of heat for heating the fluidised bed is sand which is heated using electrical heating elements to provide the energy for the endothermic reaction. Electrical energy is continuously required in order to maintain the pyroiysis reaction.
  • char produced by the pyroiysis of the bio-mass is recycled as a fuel to the pyroiysis reaction where it is combusted to provide some of the energy required to maintain the pyroiysis temperature, however, this is done at the expense of the char being lost.
  • the inventors have thus identified a need for a more efficient pyroiysis apparatus for the pyroiysis of bio-mass while reducing the need for an external energy source and possibly allowing for some or all of the char thus produced to be retained for alternative use rather than as a fuel to the pyrolysis.
  • a carbonaceous feed pyrolysis apparatus including two or more hot particle fluidised beds, and one or more positive displacement apparatus for the transfer of hot particles between two or more of the beds.
  • One or more of the fluidised beds may contain a combustion zone.
  • One or more of the fluidised beds may contain a pyrolysis zone.
  • the positive displacement apparatus may be a screw feeder or the like.
  • the screw feeder may be driven by a variable speed drive motor or a constant speed drive motor.
  • the hot particles in the fluidised beds may be sand particles.
  • the hot particles in the fluidised beds may be primarily catalyst particles.
  • the catalyst particles may be zeolite particles.
  • the catalyst particles are typically cracking catalyst particles such as acidic zeolite particles.
  • the apparatus may include one or more "L" valves between the combustion and pyrolysis zones so that hot particles may flow from the combustion zone or zones to the pyrolysis zone or zones while impeding the flow of gas in the opposite direction.
  • the apparatus as described above including a recycle duct for gas produced in the pyrolysis zone to the combustion zone for combustion for the heating of the hot particles.
  • the combustion fluidised bed may include fluidised bed nozzles whereby the fluidising gas, as well as or any combustion gasses, are injected into the fluidised bed through one or more nozzles at a base portion of the fluidised bed.
  • the pyrolysis fluidised bed may have a similar nozzle arrangement for the fluidising gas.
  • the nozzle arrangement is selected rather than the standard plenum arrangement permitting removal of the hot particles from the base of the fluidised beds by the positive displacement apparatus with a smaller hold up volume as the hot particles can drop past the nozzles for extraction.
  • Air may enter downwards or upwards through the nozzles into the fluidised beds.
  • Horizontal jets may prevent sand from flowing into an air supply line.
  • the recycle gas duct or line may enter as close as possible to the nozzle, where it mixes with cold air, and combusts in the fluidised bed.
  • the apparatus may include a char separator after the pyrolysis fluidised bed whereby char can be captured.
  • the captured char may be recycled to the combustion fluidised bed or be used for other purposes unrelated to the operation of the pyrolysis apparatus.
  • the char separator may be a cyclone.
  • a bio-oil production process including pyrolysis of a carbonaceous bio-mass, which process includes 2 or more fluidised beds, a first combustion zone carried out in one or more combustion fluidised beds in which a particulate material is fluidised and heated, and a second pyrolysis zone carried out in one or more pyrolysis fluidised beds in which the hot particles heated in the combustion zone are used for pyrolysis of the bio-mass, said combustion zone being operated at or about atmospheric pressure at a temperature of from 400°C to 1100 °C, typically around 900°C, and the pyrolysis zone being operated at a pressure of from atmospheric to 100 Barg at a temperature of from 400°C to 900°C, typically 500°C to 600 °C.
  • Pyrolysis gas from the pyrolysis zone may be at least partially recycled to the combustion zone as a source of fuel for the combustion used to heat the particles.
  • the hot particles may be sand particles, or catalyst particles as described above.
  • the pyrolysis zone may be operated at or about atmospheric pressure.
  • the use of catalyst in the pyrolysis zone may allow more throughput of bio-mass because more C0 2 is produced and therefore the reaction will be less endothermic.
  • the catalyst is typically a cracking catalyst such as an acidic zeolite.
  • the area of the combustion fluidized bed may be 2-6 times larger than that of the pyrolysis bed, typically 3 - 4 time larger. This may be more energy-efficient because less of the enthalpy available from the hot particles is used to re-heat the recycled gases, and more enthalpy is used to drive the endothermic pyrolysis reaction.
  • the superficial gas velocity (SGV) may be high in the combustion fiuidised bed at a rate of from 1 m/s to 4 m/s, typically 2 m/s, in order to burn as much oxygen as possible in a bed of a given area.
  • the superficial gas velocity of the recycle pyrolysis gas may be as low as possible while still achieving good fluidisation and thus mixing.
  • the SGV in the pyrolysis fiuidised bed may be from 0.2 to 2 m/s, typically 0.5 m/s. It is believed that in this way less enthalpy is lost by means of heating the cold recycle gas.
  • the bio-mass also enters as a solid, and leaves as a gas, thereby increasing the superficial gas velocity as the pyrolysis reaction occurs.
  • the SGV of the recycled pyrolysis gas is controlled or selected in relation to the degree of entrainment of hot particles in the combustion zone and thus if high entrainment occurs at 2.5 m/s, for instance, a low SGV of recycle pyrolysis gas can be selected in order to allow larger throughput of biomass before SGV gets unacceptably high due to vapourization of biomass.
  • Air supply to the fluidized bed may be preheated by exchanging heat from the gases exiting the combustion zone. This may substantially reduce the fluidized bed area required in the combustion zone to heat a given mass flow rate of hot particles. It also may reduce the amount of carbon that is combusted to form C0 2 , making the process more environmentally friendly.
  • the temperature of the combustion fluidized bed may be controlled by varying the rate of transfer of hot particles from the pyrolysis zone to the combustion zone, for example, by varying the speed of a motor driving the positive displacement apparatus such as a screw feeder used for the purpose.
  • the air flow rate is typically fixed to provide a constant SGV through the combustion zone.
  • Fuel flow rate (recycle gas) may be adjusted in order to ensure that there is always sufficient excess oxygen in the gas exiting from the combustion chamber. This may be estimated by measuring C0 2 concentration in the exit gases and inferring excess oxygen.
  • the temperature in the pyrolysis zone is controlled by varying the rate of bio-mass entering the pyrolysis zone.
  • the recycle gas flow rate is typically fixed in order to ensure adequate fluidization in the pyrolysis fluidized bed.
  • the fluidised beds may include disengagement zones.
  • the pressure in the disengagement zones of both the pyrolysis and combustion fluidised beds may be close to atmospheric pressure because of the difficulty of adequate sealing at high temperatures.
  • the pressure in the disengagement zone may be controlled by controlling the speed of an induced draft (ID) fan or by controlling a damper setting in a low pressure line.
  • ID induced draft
  • the pressure in the pyrolysis zone may be controlled by varying the amount of purge gas released from the recycle gas stream.
  • the combustion zone also serves to regenerate the catalyst as it burns off any coke formed in the pores of the particles during pyrolysis.
  • Figure 1 a dual fluidised bed pyrolysis apparatus of the invention
  • Figure 2 is shown a nozzle arrangement for the fluidised beds of Figure 1 ;
  • a pyrolysis apparatus 12 and a pyrolysis process is provided for rapidly heating bio- mass to be pyrolysed to bio-oil by mixing it in a pyrolysis fluidised bed 14 with hot particles, in the form of hot sand 16, from a separate fluidised bed operating in combustion conditions.
  • the combustion fluidised bed 18 has a cross sectional area 3 to 4 times that of the cross sectional area of the pyrolysis fluidised bed 14.
  • the combustion fluidised bed 18 is kept hot, typically around 900°C, by burning combustible gas and char.
  • the hot sand 16 moves from the combustion region 15 to the pyrolysis region 17 by means of an "L" valve 20 which is known in fluidised bed technology.
  • the pyrolysis reaction cools the sand down to 500-600°C, and the cooled sand is returned by a screw conveyor 22 to the hot combustion fluidised bed 18 for reheating.
  • Some char is entrained with the sand although most of the char will be entrained with the gas and will be collected by the cyclone 24.
  • the char in the sand will burn in the fluidised bed, to provide at least part of the required energy. More energy can be provided from the purge of the pyrolysis gas loop 26. 2/3 of the energy required for combustion can come from the pyrolysis gases which are combustible gases. These gases are introduced directly into the fluidised bed nozzles 28 with the recycle pyrolysis gas being fed concentricly with the air supply pipe into the fluidised bed gas feed pipes to the fluidised bed nozzles . It is preferable to use the gas as the heat source thereby saving the char, because the char is a valuable resource for farmers; it improves the soil when it is worked in.
  • the air 30 may enter the fluidised beds 14, 18 through the nozzles either downwards, as indicated, or upwards.
  • the horizontal jets are designed to prevent sand from flowing into the air supply line.
  • the gas line 32 enters as close as possible to the nozzle 34 (28), where it mixes with cold air, and combusts in the fluidized bed
  • the sand 16 that is used for the bed of the fluidised beds 14, 18 of the first embodiment is replaced with catalyst that provides a more stable bio-oil than using sand alone.
  • the oxygen content in the oil can be reduced in this way (being removed as C0 2 . Without this treatment, the oils are reactive and oligomerize over time to become an unmanageable sludge.
  • the catalytically treated oil can be blended into refinery feedstocks to form transportation fuel.
  • the dual fluidised bed system of the invention provides the ideal circumstances for continuous regeneration of the pyrolysis catalyst as the catalyst particles which are returned by the screw feeder to the combustion fluidised bed are heated to around 900°C which regenerates the catalyst continuously.
  • the flowsheet of Figure 1 is modified in that the hot sand moves from the combustion region to the pyrolysis region by means of a "Z" valve which is novel in fluidised bed technology.
  • a "Z" valve which is novel in fluidised bed technology.
  • the non-mechanical "Z" valve 36 design makes use of an angle closer to 135°, as shown between Bed A 38 (equivalent to 18 in Figure 1) and Bed B 40 (equivalent to 14 in Figure 1) in Figure 3. This allows for the unassisted transport of solids through the valve as only gravity is required as the driving force for the flow of solids.

Landscapes

  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Combustion & Propulsion (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • General Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Organic Chemistry (AREA)
  • Materials Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Dispersion Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
  • Processing Of Solid Wastes (AREA)
  • Devices And Processes Conducted In The Presence Of Fluids And Solid Particles (AREA)

Abstract

The invention provides a carbonaceous feed pyrolysis apparatus including two or more hot particle fluidised beds, and one or more positive displacement apparatus for the transfer of hot particles between two or more of the beds, wherein one or more of the fluidised beds contains a combustion zone. The invention extends to a bio-oil production process, including pyrolysis of a carbonaceous bio-mass, which process includes 2 or more fluidised beds, a first combustion zone carried out in one or more combustion fluidised beds in which a particulate material is fluidised and heated, and a second pyrolysis zone carried out in one or more pyrolysis fluidised beds in which the hot particles heated in the combustion zone are used for pyrolysis of the bio-mass, said combustion zone being operated at or about atmospheric pressure at a temperature of from 400°C to 1100 °C, typically around 900°C, and the pyrolysis zone being operated at a pressure of from atmospheric to 100 Barg at a temperature of from 400°C to 900°C.

Description

FLUIDISED BED PYROLYSIS APPARATUS AND METHOD
Field of the invention
The invention relates to the pyroiysis of carbonaceous material, such as bio-mass, in a fluidised bed pyroiysis apparatus.
Background to the Invention
Fast pyroiysis of bio-mass involves rapidly heating solid bio-mass to a temperature of 400°C to 600°C in reducing conditions so that it forms an oil. This is typically done in a fluidized bed, where approximately 60% of the original biomass can be recovered as oil. The pyroiysis is endothermic in nature, and the energy required is typically obtained by heating the fluidized bed indirectly, using electrical heating elements.
The source of heat for heating the fluidised bed is sand which is heated using electrical heating elements to provide the energy for the endothermic reaction. Electrical energy is continuously required in order to maintain the pyroiysis reaction.
In order to reduce the electrical energy demand, char produced by the pyroiysis of the bio-mass is recycled as a fuel to the pyroiysis reaction where it is combusted to provide some of the energy required to maintain the pyroiysis temperature, however, this is done at the expense of the char being lost.
The inventors have thus identified a need for a more efficient pyroiysis apparatus for the pyroiysis of bio-mass while reducing the need for an external energy source and possibly allowing for some or all of the char thus produced to be retained for alternative use rather than as a fuel to the pyrolysis.
Summary of the Invention
According to a first aspect of the invention, there is provided a carbonaceous feed pyrolysis apparatus including two or more hot particle fluidised beds, and one or more positive displacement apparatus for the transfer of hot particles between two or more of the beds.
One or more of the fluidised beds may contain a combustion zone.
One or more of the fluidised beds may contain a pyrolysis zone.
The positive displacement apparatus may be a screw feeder or the like.
The screw feeder may be driven by a variable speed drive motor or a constant speed drive motor.
The hot particles in the fluidised beds may be sand particles.
The hot particles in the fluidised beds may be primarily catalyst particles.
The catalyst particles may be zeolite particles. The catalyst particles are typically cracking catalyst particles such as acidic zeolite particles.
The apparatus may include one or more "L" valves between the combustion and pyrolysis zones so that hot particles may flow from the combustion zone or zones to the pyrolysis zone or zones while impeding the flow of gas in the opposite direction.
The apparatus as described above, including a recycle duct for gas produced in the pyrolysis zone to the combustion zone for combustion for the heating of the hot particles.
The combustion fluidised bed may include fluidised bed nozzles whereby the fluidising gas, as well as or any combustion gasses, are injected into the fluidised bed through one or more nozzles at a base portion of the fluidised bed.
The pyrolysis fluidised bed may have a similar nozzle arrangement for the fluidising gas.
In both cases the nozzle arrangement is selected rather than the standard plenum arrangement permitting removal of the hot particles from the base of the fluidised beds by the positive displacement apparatus with a smaller hold up volume as the hot particles can drop past the nozzles for extraction.
Air may enter downwards or upwards through the nozzles into the fluidised beds. Horizontal jets may prevent sand from flowing into an air supply line. The recycle gas duct or line may enter as close as possible to the nozzle, where it mixes with cold air, and combusts in the fluidised bed.
The apparatus may include a char separator after the pyrolysis fluidised bed whereby char can be captured. Typically the captured char may be recycled to the combustion fluidised bed or be used for other purposes unrelated to the operation of the pyrolysis apparatus. The char separator may be a cyclone.
According to a second aspect of the invention, there is provided a bio-oil production process, said process including pyrolysis of a carbonaceous bio-mass, which process includes 2 or more fluidised beds, a first combustion zone carried out in one or more combustion fluidised beds in which a particulate material is fluidised and heated, and a second pyrolysis zone carried out in one or more pyrolysis fluidised beds in which the hot particles heated in the combustion zone are used for pyrolysis of the bio-mass, said combustion zone being operated at or about atmospheric pressure at a temperature of from 400°C to 1100 °C, typically around 900°C, and the pyrolysis zone being operated at a pressure of from atmospheric to 100 Barg at a temperature of from 400°C to 900°C, typically 500°C to 600 °C.
Pyrolysis gas from the pyrolysis zone may be at least partially recycled to the combustion zone as a source of fuel for the combustion used to heat the particles.
The hot particles may be sand particles, or catalyst particles as described above.
The pyrolysis zone may be operated at or about atmospheric pressure.
The use of catalyst in the pyrolysis zone may allow more throughput of bio-mass because more C02 is produced and therefore the reaction will be less endothermic. The catalyst is typically a cracking catalyst such as an acidic zeolite.
The area of the combustion fluidized bed may be 2-6 times larger than that of the pyrolysis bed, typically 3 - 4 time larger. This may be more energy-efficient because less of the enthalpy available from the hot particles is used to re-heat the recycled gases, and more enthalpy is used to drive the endothermic pyrolysis reaction.
The superficial gas velocity (SGV) may be high in the combustion fiuidised bed at a rate of from 1 m/s to 4 m/s, typically 2 m/s, in order to burn as much oxygen as possible in a bed of a given area.
The superficial gas velocity of the recycle pyrolysis gas may be as low as possible while still achieving good fluidisation and thus mixing.
The SGV in the pyrolysis fiuidised bed may be from 0.2 to 2 m/s, typically 0.5 m/s. It is believed that in this way less enthalpy is lost by means of heating the cold recycle gas. The bio-mass also enters as a solid, and leaves as a gas, thereby increasing the superficial gas velocity as the pyrolysis reaction occurs. The SGV of the recycled pyrolysis gas is controlled or selected in relation to the degree of entrainment of hot particles in the combustion zone and thus if high entrainment occurs at 2.5 m/s, for instance, a low SGV of recycle pyrolysis gas can be selected in order to allow larger throughput of biomass before SGV gets unacceptably high due to vapourization of biomass.
Air supply to the fluidized bed may be preheated by exchanging heat from the gases exiting the combustion zone. This may substantially reduce the fluidized bed area required in the combustion zone to heat a given mass flow rate of hot particles. It also may reduce the amount of carbon that is combusted to form C02, making the process more environmentally friendly.
The temperature of the combustion fluidized bed may be controlled by varying the rate of transfer of hot particles from the pyrolysis zone to the combustion zone, for example, by varying the speed of a motor driving the positive displacement apparatus such as a screw feeder used for the purpose.
The air flow rate is typically fixed to provide a constant SGV through the combustion zone. Fuel flow rate (recycle gas) may be adjusted in order to ensure that there is always sufficient excess oxygen in the gas exiting from the combustion chamber. This may be estimated by measuring C02 concentration in the exit gases and inferring excess oxygen.
The temperature in the pyrolysis zone is controlled by varying the rate of bio-mass entering the pyrolysis zone. The recycle gas flow rate is typically fixed in order to ensure adequate fluidization in the pyrolysis fluidized bed.
The fluidised beds may include disengagement zones. The pressure in the disengagement zones of both the pyrolysis and combustion fluidised beds may be close to atmospheric pressure because of the difficulty of adequate sealing at high temperatures. The pressure in the disengagement zone may be controlled by controlling the speed of an induced draft (ID) fan or by controlling a damper setting in a low pressure line.
The pressure in the pyrolysis zone may be controlled by varying the amount of purge gas released from the recycle gas stream. Where catalyst particles are used instead of hot sand, the combustion zone also serves to regenerate the catalyst as it burns off any coke formed in the pores of the particles during pyrolysis.
Description of an Embodiment of the Invention
The invention will now be described, by way of non-limiting example only, with reference to the accompanying flow sheet and diagrammatic drawings, Figures 1 and 2.
In Figure 1 is shown a dual fluidised bed pyrolysis apparatus of the invention;
In Figure 2 is shown a nozzle arrangement for the fluidised beds of Figure 1 ; and
In Figure 3 is shown another embodiment of the pyrolysis apparatus of Figure 1.
In the flow sheet 10 of Figure 1 , representing an embodiment of this invention, a pyrolysis apparatus 12 and a pyrolysis process is provided for rapidly heating bio- mass to be pyrolysed to bio-oil by mixing it in a pyrolysis fluidised bed 14 with hot particles, in the form of hot sand 16, from a separate fluidised bed operating in combustion conditions.
The combustion fluidised bed 18 has a cross sectional area 3 to 4 times that of the cross sectional area of the pyrolysis fluidised bed 14. In Figure 1 , the combustion fluidised bed 18 is kept hot, typically around 900°C, by burning combustible gas and char. The hot sand 16 moves from the combustion region 15 to the pyrolysis region 17 by means of an "L" valve 20 which is known in fluidised bed technology.
The pyrolysis reaction cools the sand down to 500-600°C, and the cooled sand is returned by a screw conveyor 22 to the hot combustion fluidised bed 18 for reheating.
Some char is entrained with the sand although most of the char will be entrained with the gas and will be collected by the cyclone 24. The char in the sand will burn in the fluidised bed, to provide at least part of the required energy. More energy can be provided from the purge of the pyrolysis gas loop 26. 2/3 of the energy required for combustion can come from the pyrolysis gases which are combustible gases. These gases are introduced directly into the fluidised bed nozzles 28 with the recycle pyrolysis gas being fed concentricly with the air supply pipe into the fluidised bed gas feed pipes to the fluidised bed nozzles . It is preferable to use the gas as the heat source thereby saving the char, because the char is a valuable resource for farmers; it improves the soil when it is worked in.
As shown in Figure 2, the air 30 may enter the fluidised beds 14, 18 through the nozzles either downwards, as indicated, or upwards. The horizontal jets are designed to prevent sand from flowing into the air supply line. The gas line 32 enters as close as possible to the nozzle 34 (28), where it mixes with cold air, and combusts in the fluidized bed
In another embodiment represented by the same flowsheet of Figure 1 , the sand 16 that is used for the bed of the fluidised beds 14, 18 of the first embodiment is replaced with catalyst that provides a more stable bio-oil than using sand alone. The oxygen content in the oil can be reduced in this way (being removed as C02. Without this treatment, the oils are reactive and oligomerize over time to become an unmanageable sludge. The catalytically treated oil can be blended into refinery feedstocks to form transportation fuel.
At pyrolytic temperatures, catalysts are prone to coking, which deactivates them. They will last just 5 minutes at these conditions. The catalyst can be renewed by burning off the carbon. The dual fluidised bed system of the invention provides the ideal circumstances for continuous regeneration of the pyrolysis catalyst as the catalyst particles which are returned by the screw feeder to the combustion fluidised bed are heated to around 900°C which regenerates the catalyst continuously.
In Figure 3, the flowsheet of Figure 1 is modified in that the hot sand moves from the combustion region to the pyrolysis region by means of a "Z" valve which is novel in fluidised bed technology. Unlike L-valves 20 of Figure 1 , in which the bottom pipe section is at 90° from the vertical, the non-mechanical "Z" valve 36 design makes use of an angle closer to 135°, as shown between Bed A 38 (equivalent to 18 in Figure 1) and Bed B 40 (equivalent to 14 in Figure 1) in Figure 3. This allows for the unassisted transport of solids through the valve as only gravity is required as the driving force for the flow of solids.
It is believed to be an advantage of the invention that more efficient pyrolisis is achieved as well as better quality bio-oil, while char which is produced can be used for other purposes.

Claims

Claims
1. A carbonaceous feed pyrolysis apparatus including two or more hot particle fluidised beds, and one or more positive displacement apparatus for the transfer of hot particles between two or more of the beds.
2. An apparatus as claimed in claim 1 , wherein one or more of the fluidised beds contains a combustion zone.
3. An apparatus as claimed in claim 1 or claim 2, wherein one or more of the fluidised beds contains a pyrolysis zone.
4. An apparatus as claimed in any of the preceding claims, wherein the positive displacement apparatus is a screw feeder driven by a variable speed drive motor or a constant speed drive motor.
5. An apparatus as claimed in any one of the preceding claims, wherein the hot particles in the fluidised beds are sand particles.
6. An apparatus as claimed in any one of claims 1 to 4, wherein the hot particles in the fluidised beds are primarily catalyst particles.
7. An apparatus as claimed in claim 6, wherein the catalyst particles are zeolite particles.
An apparatus as claimed in claim 6 or claim 7, wherein the catalyst particles cracking catalyst particles.
9. An apparatus as claimed in any one of the preceding claims, wherein the apparatus includes one or more valve means between the combustion and pyrolysis zones so that hot particles flow from the combustion zone or zones to the pyrolysis zone or zones while impeding the flow of gas in the opposite direction.
10. An apparatus as claimed in any one of the preceding claims, wherein the apparatus includes a recycle duct for gas produced in the pyrolysis zone to the combustion zone for combustion for the heating of the hot particles.
11. An apparatus as claimed in any one of claims 2 to 10, wherein the combustion fluidised includes fluidised bed nozzles whereby the fluidising gas, as well as or any combustion gasses, are injected into the fluidised bed through one or more nozzles at a base portion of the fluidised bed.
12. An apparatus as claimed in any one of claims 3 to 10, wherein the pyrolysis fluidised bed has a similar nozzle arrangement for the fluidising gas.
13. An apparatus as claimed in claim 11 or claim 12, wherein the nozzle arrangement permits removal of the hot particles from the base of the fluidised beds by the positive displacement apparatus with a smaller hold up volume as the hot particles drop past the nozzles for extraction.
14. An apparatus as claimed in any one of claims 11 to 13, wherein air enters downwards or upwards through the nozzles into the fluidised beds.
15. An apparatus as claimed in any one of claims 3 to 14, wherein the apparatus includes a char separator after the pyrolysis fluidised bed whereby char is captured.
16. A bio-oil production process, said process including pyrolysis of a carbonaceous bio-mass, which process includes 2 or more fluidised beds, a first combustion zone carried out in one or more combustion fluidised beds in which a particulate material is fluidised and heated, and a second pyrolysis zone carried out in one or more pyrolysis fluidised beds in which the hot particles heated in the combustion zone are used for pyrolysis of the bio-mass, said combustion zone being operated at or about atmospheric pressure at a temperature of from 400°C to 1100 °C, typically around 900°C, and the pyrolysis zone being operated at a pressure of from atmospheric to 100 Barg at a temperature of from 400°C to 900°C.
17. A process as claimed in claim 16, wherein the pyrolysis zone is operated at a temperature of 500°C to 600 °C.
18. A process as claimed in claim 16 or claim 17, wherein pyrolysis gas from the pyrolysis zone is at least partially recycled to the combustion zone as a source of fuel for the combustion used to heat the particles.
19. A process as claimed in any one of claims 16 to 18, wherein the hot particles are sand particles or catalyst particles.
20. A process as claimed in any one of claims 16 to 19, wherein the pyrolysis zone is operated at or about atmospheric pressure.
21. A process as claimed in claim 19, wherein the use of catalyst in the pyrolysis zone allows more throughput of bio-mass because more C02 is produced and therefore the reaction will be less endothermic.
22. A process as claimed in claim 19 or claim 21 , wherein the catalyst is a cracking catalyst.
23. A process as claimed in claim 22, wherein the catalyst is an acid zeolite catalyst.
24. A process as claimed in any one of claims 16 to 23, wherein the area of the combustion fluidized bed is 2-6 times larger than that of the pyrolysis bed.
25. A process as claimed in claim 24, wherein the area of the combustion fluidized bed is 3 - 4 times larger than that of the pyrolysis bed.
26. A process as claimed in any one of claims 16 to 25, wherein the superficial gas velocity (SGV) is high in the combustion fluidised bed at a rate of from 1 m/s to 4 m/s in order to burn as much oxygen as possible in a bed of a given area.
27. A process as claimed in any one of claims 16 to 25, wherein the superficial gas velocity (SGV) is high in the combustion fluidised bed at a rate of 2 m/s in order to burn as much oxygen as possible in a bed of a given area.
28. A process as claimed in any one of the preceding claims, wherein the SGV in the pyrolysis fluidised bed is from 0.2 to 2 m/s.
29. A process as claimed in any one of the preceding claims, wherein the SGV in the pyrolysis fluidised bed is 0.5 m/s.
30. A process as claimed in any one of claims 18 to 29, wherein the SGV of the recycled pyrolysis gas is controlled or selected in relation to the degree of entrainment of hot particles in the combustion zone.
31. A process as claimed in any one of claims 16 to 30, wherein the air supply to the fluidized bed is preheated by exchanging heat from the gases exiting the combustion zone.
32. A process as claimed in any one of claims 16 to 31 , wherein the temperature of the combustion fluidized bed is controlled by varying the rate of transfer of hot particles from the pyrolysis zone to the combustion zone.
33. A process as claimed in claim 32, wherein the varying of the rate of transfer of hot particles is achieved by varying the speed of a motor driving the positive displacement apparatus used for the purpose.
34. A process as claimed in any one of claims 16 to 33, wherein the temperature in the pyrolysis zone is controlled by varying the rate of bio-mass entering the pyrolysis zone.
35. A process as claimed in any one of claims 16 to 34, wherein the recycle gas flow rate is fixed in order to ensure adequate fluidization in the pyrolysis fluidized bed.
36. A process as claimed in any one of claims 16 to 35, wherein the fluidised beds include disengagement zones.
37. A process as claimed in claim 36, wherein the pressure in the disengagement zones of both the pyrolysis and combustion fluidised beds are close to atmospheric pressure because of the difficulty of adequate sealing at high temperatures.
38. A process as claimed in claim 37, wherein the pressure in the disengagement zone is controlled by controlling the speed of an induced draft (ID) fan or by controlling a damper setting in a low pressure line.
39. A process as claimed in any one of claims 16 to 38, wherein the pressure in the pyrolysis zone is controlled by varying the amount of purge gas released from the recycle gas stream.
40. A process as claimed in any one of claims 19 to 39, wherein where catalyst particles are used as the hot particles, the combustion zone also serves to regenerate the catalyst as it burns off any coke formed in the pores of the particles during pyrolysis.
41. An apparatus as claimed in claim 9, wherein the valve is a non-mechanical valve making use of an angle between 120° and 150°, typically 135° between between the combustion and pyrolysis zones so that hot particles flow from the combustion zone or zones to the pyrolysis zone or zones while impeding the flow of gas in the opposite direction.
PCT/ZA2011/000067 2010-09-10 2011-09-08 Fluidised bed pyrolysis apparatus and method Ceased WO2012034141A1 (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
US13/820,721 US9580657B2 (en) 2010-09-10 2011-09-08 Fluidised bed pyrolysis apparatus and method
BR112013005718A BR112013005718B1 (en) 2010-09-10 2011-09-08 carbonaceous pyrolysis apparatus, and bio-oil production process
EP11782355.9A EP2614128B1 (en) 2010-09-10 2011-09-08 Fluidised bed pyrolysis apparatus and method
CA2810724A CA2810724C (en) 2010-09-10 2011-09-08 Fluidised bed pyrolysis apparatus and method
CN201180049338.0A CN103180412B (en) 2010-09-10 2011-09-08 Fluidized bed cracking apparatus and method

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US38191710P 2010-09-10 2010-09-10
US61/381,917 2010-09-10

Publications (2)

Publication Number Publication Date
WO2012034141A1 true WO2012034141A1 (en) 2012-03-15
WO2012034141A4 WO2012034141A4 (en) 2012-05-03

Family

ID=44947268

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/ZA2011/000067 Ceased WO2012034141A1 (en) 2010-09-10 2011-09-08 Fluidised bed pyrolysis apparatus and method

Country Status (5)

Country Link
US (1) US9580657B2 (en)
EP (1) EP2614128B1 (en)
BR (1) BR112013005718B1 (en)
CA (1) CA2810724C (en)
WO (1) WO2012034141A1 (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2015003193A3 (en) * 2013-06-14 2015-12-23 University Of Pretoria Apparatus for endothermic reactions
US9434885B2 (en) 2013-02-26 2016-09-06 The United States Of America, As Represented By The Secretary Of Agriculture Methods for producing bio-oil
EP3656834A1 (en) * 2013-02-20 2020-05-27 Recycling Technologies Ltd Portable apparatus for treating waste comprising mixed plastic waste
WO2021074626A1 (en) * 2019-10-16 2021-04-22 Recycling Technologies Ltd Improvements in and relating to reactor fluid supply systems
WO2022056559A1 (en) 2020-09-14 2022-03-17 University Of Pretoria Fluidised bed pyrolysis apparatus and method

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR3029979B1 (en) * 2014-12-12 2019-04-05 IFP Energies Nouvelles METHOD AND INSTALLATION OF COMBUSTION BY OXYDO-CHEMICAL LOOP REDUCTION OF A GAS HYDROCARBONATED LOAD WITH IN SITU CATALYTIC REFORMING OF THE LOAD
JP6809197B2 (en) * 2016-12-16 2021-01-06 株式会社Ihi Fluidized bed system
FI127753B (en) 2017-06-09 2019-01-31 Bioshare Ab Recovery of chemicals from fuel streams
CN110437858A (en) * 2019-08-26 2019-11-12 华南理工大学 Method and device for microwave-assisted catalytic rapid pyrolysis of domestic waste with regenerable catalyst
US12319878B2 (en) 2020-08-06 2025-06-03 Chevron U.S.A. Inc. Upgrading of low value lipid feedstocks for refinery processing
AU2021107412A4 (en) * 2021-06-23 2021-12-23 SEATA Holdings Pty Ltd Process of treating carbonaceous material and apparatus therefor
EP4209710A1 (en) * 2022-01-10 2023-07-12 ICMEA Srl leader of temporary association of companies ICMEA Srl - Tecnomec Engineering Srl - CNR IRSA Fluidised bed unit
US12421460B2 (en) 2024-01-15 2025-09-23 Chevron U.S.A. Inc. Downflow lipid conversion with upflow catalyst regeneration
WO2025155623A1 (en) 2024-01-16 2025-07-24 Chevron U.S.A. Inc. Catalyst selection for improved lipid feedstock conversion
US12319881B1 (en) 2024-09-27 2025-06-03 Chevron U.S.A. Inc. Converting a renewable fuel intermediate composition to finished transportation fuel
US12582954B1 (en) 2024-12-13 2026-03-24 Chevron U.S.A. Inc. Processing feedstocks
US12590258B1 (en) 2025-02-28 2026-03-31 Chevron U.S.A. Inc. Converting a lipid feedstock to fuel

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4311670A (en) * 1976-09-22 1982-01-19 A. Ahlstrom Osakeyhtio Fluidized bed reactor system
US4823712A (en) * 1985-12-18 1989-04-25 Wormser Engineering, Inc. Multifuel bubbling bed fluidized bed combustor system
WO1994024228A1 (en) * 1993-04-20 1994-10-27 Valtion Teknillinen Tutkimuskeskus Process for the production of liquid fuel, gaseous fuel, coke and active coal
DE19517096A1 (en) * 1995-05-10 1996-11-14 Daniel Engelhardt Pyrolysis process for plastics operating at relatively low temps.

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1448196A (en) * 1972-10-20 1976-09-02 Sprocket Properties Ltd Fluidised bed incinerators
US4279207A (en) * 1979-04-20 1981-07-21 Wormser Engineering, Inc. Fluid bed combustion
BR112012005379B1 (en) * 2009-09-09 2019-03-06 University Of Massachusetts SYSTEMS AND PROCESSES FOR CATALYTIC BIOMASS PYROLYSIS AND HYDROCARBONIFIC MATERIALS FOR PRODUCTION OF OPTIONAL OLEPHINE RECYCLING AND CATALYLERS HAVING SELECTED PARTICLE SIZE FOR CATALYTIC PYROLYSIS.

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4311670A (en) * 1976-09-22 1982-01-19 A. Ahlstrom Osakeyhtio Fluidized bed reactor system
US4823712A (en) * 1985-12-18 1989-04-25 Wormser Engineering, Inc. Multifuel bubbling bed fluidized bed combustor system
WO1994024228A1 (en) * 1993-04-20 1994-10-27 Valtion Teknillinen Tutkimuskeskus Process for the production of liquid fuel, gaseous fuel, coke and active coal
DE19517096A1 (en) * 1995-05-10 1996-11-14 Daniel Engelhardt Pyrolysis process for plastics operating at relatively low temps.

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
AHO A ET AL: "Catalytic pyrolysis of woody biomass in a fluidized bed reactor: Influence of the zeolite structure", FUEL, IPC SCIENCE AND TECHNOLOGY PRESS, GUILDFORD, GB, vol. 87, no. 12, 1 September 2008 (2008-09-01), pages 2493 - 2501, XP022679779, ISSN: 0016-2361, [retrieved on 20080314], DOI: 10.1016/J.FUEL.2008.02.015 *

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3656834A1 (en) * 2013-02-20 2020-05-27 Recycling Technologies Ltd Portable apparatus for treating waste comprising mixed plastic waste
US10717934B2 (en) 2013-02-20 2020-07-21 Recycling Technologies Ltd. Apparatus for treating waste comprising mixed plastic waste
US10760003B2 (en) 2013-02-20 2020-09-01 Recycling Technologies Ltd Process and apparatus for treating waste comprising mixed plastic waste
US9434885B2 (en) 2013-02-26 2016-09-06 The United States Of America, As Represented By The Secretary Of Agriculture Methods for producing bio-oil
WO2015003193A3 (en) * 2013-06-14 2015-12-23 University Of Pretoria Apparatus for endothermic reactions
US10041003B2 (en) 2013-06-14 2018-08-07 University Of Pretoria Apparatus for endothermic reactions
US10731083B2 (en) 2013-06-14 2020-08-04 University Of Pretoria Apparatus for endothermic reactions
WO2021074626A1 (en) * 2019-10-16 2021-04-22 Recycling Technologies Ltd Improvements in and relating to reactor fluid supply systems
EP4045850B1 (en) * 2019-10-16 2025-04-23 Deeptech Recycling Limited Improvements in and relating to reactor fluid supply systems
US12344801B2 (en) 2019-10-16 2025-07-01 DeepTech Recycling Reactor fluid supply systems
WO2022056559A1 (en) 2020-09-14 2022-03-17 University Of Pretoria Fluidised bed pyrolysis apparatus and method

Also Published As

Publication number Publication date
WO2012034141A4 (en) 2012-05-03
CA2810724A1 (en) 2012-03-15
BR112013005718A2 (en) 2017-04-04
EP2614128B1 (en) 2019-08-21
CA2810724C (en) 2018-05-01
US9580657B2 (en) 2017-02-28
CN103180412A (en) 2013-06-26
BR112013005718B1 (en) 2019-12-24
US20140008205A1 (en) 2014-01-09
EP2614128A1 (en) 2013-07-17

Similar Documents

Publication Publication Date Title
CA2810724C (en) Fluidised bed pyrolysis apparatus and method
US10794588B2 (en) Apparatuses for controlling heat for rapid thermal processing of carbonaceous material and methods for the same
US20100162625A1 (en) Biomass fast pyrolysis system utilizing non-circulating riser reactor
CN101775296B (en) Process and device for dry distillation of lignite on basis of coke-carried heat
CN101691501B (en) Coal-grading conversion poly-generation device and method for producing coal gas, tar and carbocoal on circulating fluid bed
CN112513225A (en) Pyrolysis reaction system and method for pyrolyzing organic feed
CN106010672A (en) Char-handling processes in a pyrolysis system
CN101358136A (en) Method and device for direct fluidized bed coking of oil sand
US12270002B2 (en) Process of treating carbonaceous material and apparatus therefor
CN105316014A (en) Method and system for pyrolyzing biomass
CN105273731A (en) Biomass pyrolysis gas/charcoal co-production device and process
CN102952555A (en) Gaseous pyrolysis product collector and carbonaceous material pyrolysis or dry distillation device using same
CN101362955B (en) Pyrolysis method and device of low speed bed
US20230357641A1 (en) Fluidised bed pyrolysis apparatus and method
US4413573A (en) Process for combusting carbonaceous solids containing nitrogen
CN105331377A (en) Coal pyrolysis method and system
JPS58171483A (en) Solid carbonaceous particle thermal decomposition and retort thermal decomposition reactor
AU2021107412A4 (en) Process of treating carbonaceous material and apparatus therefor
JP2007217696A (en) Material production system and gas supply method
US2773018A (en) Continuous process for drying, preheating, and devolatilization of carbonaceous materials
JP3990897B2 (en) Gas supply apparatus and gas supply method
JP2003042421A (en) Gas supply device and gas supply method
CN109929578B (en) Coal dry distillation process and system with CO2 as heat carrier
CN103180412B (en) Fluidized bed cracking apparatus and method
CN106367123B (en) A kind of gasification production method of high calorific value synthesis gas and device for realizing the method

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 11782355

Country of ref document: EP

Kind code of ref document: A1

ENP Entry into the national phase

Ref document number: 2810724

Country of ref document: CA

NENP Non-entry into the national phase

Ref country code: DE

WWE Wipo information: entry into national phase

Ref document number: 2011782355

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 13820721

Country of ref document: US

REG Reference to national code

Ref country code: BR

Ref legal event code: B01A

Ref document number: 112013005718

Country of ref document: BR

ENP Entry into the national phase

Ref document number: 112013005718

Country of ref document: BR

Kind code of ref document: A2

Effective date: 20130308