EP2655566A1 - Process for producing synthesis gas - Google Patents
Process for producing synthesis gasInfo
- Publication number
- EP2655566A1 EP2655566A1 EP11799698.3A EP11799698A EP2655566A1 EP 2655566 A1 EP2655566 A1 EP 2655566A1 EP 11799698 A EP11799698 A EP 11799698A EP 2655566 A1 EP2655566 A1 EP 2655566A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- biomass
- carbonaceous feedstock
- process according
- feedstock
- carbonaceous
- 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- Withdrawn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
- 238000000034 method Methods 0.000 title claims abstract description 53
- 230000008569 process Effects 0.000 title claims abstract description 51
- 230000015572 biosynthetic process Effects 0.000 title claims abstract description 25
- 238000003786 synthesis reaction Methods 0.000 title claims abstract description 25
- 239000002028 Biomass Substances 0.000 claims abstract description 112
- 238000002309 gasification Methods 0.000 claims abstract description 37
- 239000007789 gas Substances 0.000 claims abstract description 34
- 238000006243 chemical reaction Methods 0.000 claims abstract description 19
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 17
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 17
- 238000002156 mixing Methods 0.000 claims abstract description 8
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims abstract description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 3
- 229910002091 carbon monoxide Inorganic materials 0.000 claims abstract description 3
- 239000001257 hydrogen Substances 0.000 claims abstract description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 3
- 230000001590 oxidative effect Effects 0.000 claims abstract description 3
- 239000003245 coal Substances 0.000 claims description 22
- 239000007787 solid Substances 0.000 claims description 22
- 239000000203 mixture Substances 0.000 claims description 17
- 239000000446 fuel Substances 0.000 claims description 13
- 239000007788 liquid Substances 0.000 claims description 10
- 238000000197 pyrolysis Methods 0.000 claims description 9
- 239000002002 slurry Substances 0.000 claims description 8
- 238000001722 flash pyrolysis Methods 0.000 claims description 6
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 3
- 229910001882 dioxygen Inorganic materials 0.000 claims description 3
- 239000000376 reactant Substances 0.000 claims description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 15
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 14
- 239000001301 oxygen Substances 0.000 description 14
- 229910052760 oxygen Inorganic materials 0.000 description 14
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 8
- 238000001816 cooling Methods 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 230000003647 oxidation Effects 0.000 description 7
- 238000007254 oxidation reaction Methods 0.000 description 7
- 239000002893 slag Substances 0.000 description 7
- 239000002023 wood Substances 0.000 description 6
- 239000002956 ash Substances 0.000 description 5
- 239000001569 carbon dioxide Substances 0.000 description 4
- 150000002430 hydrocarbons Chemical class 0.000 description 4
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 235000019198 oils Nutrition 0.000 description 4
- 238000010791 quenching Methods 0.000 description 4
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- 239000012159 carrier gas Substances 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 239000002699 waste material Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 239000003034 coal gas Substances 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 239000010881 fly ash Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 238000005453 pelletization Methods 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 230000000171 quenching effect Effects 0.000 description 2
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- 240000003133 Elaeis guineensis Species 0.000 description 1
- 235000001950 Elaeis guineensis Nutrition 0.000 description 1
- 235000019482 Palm oil Nutrition 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- RHZUVFJBSILHOK-UHFFFAOYSA-N anthracen-1-ylmethanolate Chemical compound C1=CC=C2C=C3C(C[O-])=CC=CC3=CC2=C1 RHZUVFJBSILHOK-UHFFFAOYSA-N 0.000 description 1
- 239000003830 anthracite Substances 0.000 description 1
- 239000010426 asphalt Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000012075 bio-oil Substances 0.000 description 1
- 239000003225 biodiesel Substances 0.000 description 1
- 239000002551 biofuel Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 238000004523 catalytic cracking Methods 0.000 description 1
- 238000004517 catalytic hydrocracking Methods 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000003250 coal slurry Substances 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000005094 computer simulation Methods 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 239000010791 domestic waste Substances 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000003077 lignite Substances 0.000 description 1
- 239000002029 lignocellulosic biomass Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- GBMDVOWEEQVZKZ-UHFFFAOYSA-N methanol;hydrate Chemical compound O.OC GBMDVOWEEQVZKZ-UHFFFAOYSA-N 0.000 description 1
- 239000003595 mist Substances 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- 239000003415 peat Substances 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 239000002006 petroleum coke Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000010248 power generation Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000004886 process control Methods 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000004227 thermal cracking Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
- C10J3/00—Production of combustible gases containing carbon monoxide from solid carbonaceous fuels
- C10J3/72—Other features
- C10J3/723—Controlling or regulating the gasification process
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
- C10J3/00—Production of combustible gases containing carbon monoxide from solid carbonaceous fuels
- C10J3/02—Fixed-bed gasification of lump fuel
- C10J3/20—Apparatus; Plants
- C10J3/30—Fuel charging devices
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
- C10J3/00—Production of combustible gases containing carbon monoxide from solid carbonaceous fuels
- C10J3/58—Production of combustible gases containing carbon monoxide from solid carbonaceous fuels combined with pre-distillation of the fuel
- C10J3/60—Processes
- C10J3/64—Processes with decomposition of the distillation products
- C10J3/66—Processes with decomposition of the distillation products by introducing them into the gasification zone
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
- C10J2300/00—Details of gasification processes
- C10J2300/09—Details of the feed, e.g. feeding of spent catalyst, inert gas or halogens
- C10J2300/0913—Carbonaceous raw material
- C10J2300/0916—Biomass
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
- C10J2300/00—Details of gasification processes
- C10J2300/09—Details of the feed, e.g. feeding of spent catalyst, inert gas or halogens
- C10J2300/0913—Carbonaceous raw material
- C10J2300/0926—Slurries comprising bio-oil or bio-coke, i.e. charcoal, obtained, e.g. by fast pyrolysis of biomass
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
- C10J2300/00—Details of gasification processes
- C10J2300/09—Details of the feed, e.g. feeding of spent catalyst, inert gas or halogens
- C10J2300/0913—Carbonaceous raw material
- C10J2300/093—Coal
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
- C10J2300/00—Details of gasification processes
- C10J2300/09—Details of the feed, e.g. feeding of spent catalyst, inert gas or halogens
- C10J2300/0913—Carbonaceous raw material
- C10J2300/094—Char
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
- C10J2300/00—Details of gasification processes
- C10J2300/18—Details of the gasification process, e.g. loops, autothermal operation
- C10J2300/1846—Partial oxidation, i.e. injection of air or oxygen only
-
- 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 present invention relates to a process for producing synthesis gas stream from a carbonaceous feedstock, which process includes biomass fuel as a means to control the carbon conversion at a given gasification temperature in a gasification process.
- WO 03/012013 describes a process for the incomplete combustion of domestic waste to produce syngas.
- the process as described may also include controlling the temperature in various parts of the reaction space by controlling the temperature of the oxygen-containing gas fed thereto, controlling the rate of feed of the waste and the resulting ratio of the waste feed to the oxygen- containing gas feed, and thermally insulating the reation space .
- JP2002194363 describes a method for the pressurized entrained bed gasification of coal, by which biomass can be used to efficiently lower high heat generated by gasification of the coal, thereby reducing the occurrence of problems with the accumulation and fusion of ash on the operation of a pressurized entrained bed gasification furnace.
- the method is characterized by introducing coal particles into the lower portion of the pressurized entrained bed gasification furnace to produce the high temperature coal gas, introducing a biomass fuel into the upper portion to bring into contact with the high
- a carbonaceous feedstock such as coal may be mixed with biomass prior to the mixture being introduced into the burner section of the - - gasifier.
- the mixing of biomass with the coal in such a manner helps to ensure synergy between the oxygen rich biomass and oxygen lean carbonaceous feedstocks. Due to the high oxygen content in the biomass feedstock, the requirement of a moderator gas to obtain full conversion of the carbonaceous feedstock at a given gasification temperature is reduced and can even be eliminated at sufficient high fractions of biomass in the coal/biomass mixture.
- moderator gas steam or carbon dioxide or a combination thereof is typically used.
- An object of the present invention is to provide a simplified, energy efficient and renewable means of controlling the carbonaceous feedstock conversion by mixing in a biomass fuel.
- Biomass in general has a high oxygen content and can provide part of the oxygen
- a certain minimum biomass fraction in the biomass/carbonaceous feedstock mixture is required to eliminate the steam. This fraction is
- a process for controlling the carbon conversion of a gasifier fuelled with a carbonaceous feedstock by mixing in biomass comprising the steps of
- feedstock/biomass with a molecular oxygen-comprising gas to obtain a synthesis gas comprising carbon monoxide and hydrogen;
- said gasifier feed comprises from a minimum of 10 wt% to 50 wt%, preferably 10 wt% to 30 wt% of biomass and wherein the level of biomass may adjusted within this range as needed to control the carbon conversion and reduce or eliminate the moderator gas demand.
- synthesis gas produced by this process may also contain water, hydrogen sulphide and carbon dioxide.
- the temperature in the gasifier can be
- biomass/carbonaceous fuel ratio thereby simplifying process control.
- step (a) pressurization may be accomplished by a lock hopper system or (solids) pumps.
- a lock hopper system is generally used to pressurize dry and solid feedstocks.
- a pump can be used to pressurize liquid or - - slurry (mixture of solids and liquid) feedstocks.
- a solids pump can also be applied to pressurize solid feedstocks .
- step (b) pulverized or liquid/slurry biomass can be mixed with the carbonaceous feed or fed separately to the gasifier.
- a separate feedline for the biomass to the gasification reactor is preferred as this will reduce the response time on a step change from the carbon conversion controller significantly.
- Mixing of the biomass with the carbonaceous feed can be done at several locations in the fuel preparation and pressurization section.
- step (c) any type of coal or oil burner
- the biomass When the biomass is supplied separately to the gasification reactor then the biomass may also be introduced through a nozzle in the burner area of the gasification reactor. The oxygen for the partial oxidation of the biomass will then need to be supplied via the carbonaceous fuel burner.
- step (c) the carbonaceous/biomass feedstock is subjected to partial oxidation with a molecular oxygen comprising gas.
- the partial oxidation is preferably performed at a temperature of between 1000 and 1800 °C and more preferably at a temperature between 1200 and 1800 °C.
- the pressure at which partial oxidation is performed is preferably between 0.3 and 12 MPa and preferably between 3 and 10 MPa.
- the temperature conditions are so chosen that a slag layer will form on the interior of the reactor vessel in which the partial oxidation takes place.
- step (d) the C02 content is preferably measured in cleaned and cold syngas, for example downstream of the wet scrubber.
- a fast measurement is preferred to minimize - - the time between a step change in C02 concentration and the control action.
- An infrared based analyser is an example of such a fast measurement device.
- step (d) the C02 content of the syngas is
- step (e) a
- controller will subsequently adjust the biomass/coal ratio by preferably changing the set-point of the biomass feed rate controller.
- the carbonaceous feedstock is preferably coal, as for example anthracite, brown coal, bitumous coal, and sub- bitumous coal.
- Examples of alternative carbonaceous feedstocks are petroleum coke, peat and heavy residues as extracted from tar sands or the asphalt fraction as separated from said residues in a de-asphalting process. Residues from refineries such as residual oil fractions boiling above 360 °C, directly derived from crude oil, or from oil conversion processes such as thermal cracking, catalytic cracking, hydrocracking etc may also be used as the carbonaceous feedstock.
- moisture content of typically lower than 20 wt% and which can be ground to particles with sizes between 10 and 1000 micron are suitable solid biomass feedstocks comprising the 10 wt% to 50 wt% biomass component of the
- Torrefaction of a biomass source are suitable as well and are preferred at higher biomass fractions in the mixture. Torrefaction is preferably combined with a compression or pelletization step in order to make the biomass feed more suited for a gasification process wherein the biomass feed is supplied in a so-called dry form or slurry form when torrefied particles are mixed with a carbonaceous liquid. Torrefaction of biomass source material is well - - known and for example described in M. Pach, R. Zanzi and E. Bjornbom, Torrefied Biomass a Substitute for Wood and Charcoal. 6th Asia-Pacific International Symposium on Combustion and Energy Utilization. May 2002, Kuala Lumpur and in Bergman, P.C.A., "Torrefaction in combination with pelletisation - the TOP process", ECN Report,
- Another suitable solid biomass fuel in the present process is obtained by drying and slow pyrolysis of a biomass source.
- slow pyrolysis processes a solid char feed component is typically obtained.
- Slow pyrolysis is well known and for example described In: "Pyrolysis and Other Thermal Processing” . US DOE 14-08-2007.
- a suitable liquid or solid biomass feedstock for use in the present process is obtained by drying and flash pyrolysis of a biomass source.
- flash pyrolysis In flash pyrolysis
- Flash pyrolysis is well known and for example described in EP-A-904335; in Dinesh Mohan, Charles U. Pittman, Jr., and Philip H. Steele. Pyrolysis of Wood/Biomass for Bio-oil: A Critical Review. Energy & Fuels 2006, 20, 848-889; and in E.
- the present invention is also directed to embodiments wherein a so-called biomass slurry is used as feedstock.
- the slurry can be obtained by mixing the pyrolysis oil and char.
- Suitable biomass sources are weeds or residues of the agricultural industry.
- suitable residue - - products are streams generated in the palm oil industry, corn industry, bio-diesel industry, forestry industry, wood processing industry and paper industry.
- Certain biomass is relatively expensive—for example, wood
- the present invention now provides for a process whereby the partial oxidation of a carbonaceous feedstock is performed in an efficient manner thereby obtaining synthesis gas with a reduced carbon footprint suited for catalytic conversion reactions.
- An especially interesting catalytic conversion reaction is a hydrocarbon synthesis process.
- synthesis gas is catalytically converted into hydrocarbon compounds ranging from methane to high molecular weight molecules comprising up to 200 carbon atoms, or, under particular circumstances, even more.
- An example of a hydrocarbon synthesis process is the Fischer-Tropsch process, described in e.g. WO 02/02489, WO 01/76736, WO 02/07882, EP 510771 and EP 450861.
- Step (c) may be performed by means of various
- gasification processes such as for example the so-called moving bed process, fluid bed gasifier process or the entrained-flow gasifier process as for example described in Gasification, by Christofer Higman and Maart van der
- an entrained-flow gasifier is used because the process can handle a large variety of - - feedstock and because a tar-free synthesis gas is
- the feedstock and oxygen are introduced into the reactor co-currently, preferably by means of a suitable burner.
- suitable burners and their preferred uses are described in US-A-4510874 and in US-A-4523529.
- the operating conditions are such that the process is operated in a slagging mode, which means that the operating temperature is above the ash melting point.
- the carbonaceous feedstock and the molecular oxygen comprising gas is converted to synthesis gas by providing said reactants to a burner as present in a gasification reactor at a pressure of between 3 and 10 MPa and preferably at a pressure between 4 and 8 MPa.
- the operating temperature is suitably between 1200 and 1800°C.
- the synthesis gas is preferably cooled to a temperature of below 1000°C, preferably below 500°C with either direct quenching with evaporating water, direct quenching with a methanol-water mixture, by indirect heat exchange against evaporating water or combination of such cooling steps. Slag and other molten solids are suitably discharged from the gasification reactor at the lower end of the said reactor.
- a solid carbonaceous feedstock/biomass feed mixture may be provided to the burner of the entrained flow gasifier reactor as a slurry in water.
- Coal slurry feeding processes are for example described in EP-A- 168128.
- feedstock/biomass feedstock is provided to the burner in a gas-solids mixture comprising the solid feed in the form of a powder and a suitable carrier gas.
- suitable carrier gasses are nitrogen, carbon dioxide, natural gas or synthesis gas, i.e. a mixture comprising of CO and 3 ⁇ 4 .
- the carrier gas is preferably carbon dioxide.
- the use of - - this carrier gas is for example described in WO-A- 2007042562.
- Figure 1 shows a preferred embodiment of the present invention .
- Figure 1 schematically shows a system for producing and cleaning synthesis gas.
- a gasification reactor 9 a carbonaceous feed, a biomass feed and an oxygen
- the biomass can be fed separately via line
- the carbonaceous stream 8 and biomass stream 25 are at least partially oxidised in the gasification reactor 9, thereby obtaining a raw synthesis gas 10 and a slag. To this end usually several burners (not shown) are present in the
- the biomass stream 25 can also be introduced in the gasification reactor 9 via nozzles in the burner area of gasification reactor, for example at burner level. Then the oxygen for the partial oxidation of the biomass will be added to the burner oxygen of the carbonaceous stream 8.
- the carbon conversion of the gasifier is controlled with controller 18.
- Input for the carbon conversion controller is the measured C02 content of the syngas 16 downstream of the wet scrubber 15 with the C02 analyser 17.
- the C02 content drops below a pre ⁇ determined value than the biomass/coal ratio needs to be increased by changing the biomass feed 3 and increasing the flow rate of line 5 or 25.
- the biomass/coal ratio can be reduced by changing - - the biomass feed 3 and decreasing the flow rate of line 4 or 25.
- the C02 analyser and benefits for controlling the steam and oxygen to carbon (O/C) ratio are described in WO2008125556A1 and W0200768684A2.
- An advantage for the use of biomass to control the carbon conversion is that a C02 neutral feedstock is used, which reduces the C02 footprint of the plant.
- this application reduces the high pressure steam and high quality boiler feed water requirements for the gasification island.
- the produced raw synthesis gas is fed via line 10 to a cooling section 11; herein the raw synthesis gas is usually cooled to about 200-400 °C.
- the cooling section 11 may be an indirect heat exchanger or a quench vessel.
- liquid water is preferably injected via line 23 into a synthesis gas stream.
- Liquid water is preferably injected in the form of a mist.
- the cooling section 11 can be integrated in the gasification reactor pressure vessel at the bottom of the reactor or installed as a separate vessel. When the syngas and slag both exit at the bottom of the
- the cooling section 11 is integrated in the pressure vessel and both the syngas and fly ash and slag will enter the cooling section.
- the syngas leaves the gasification reactor 9 at the top and slag at the bottom then only syngas with fly ash will enter the cooling section that is installed as separate section downstream of the reactor.
- the raw synthesis gas leaving the cooling section 10 is further processed. To this end, it is fed via line 12 into a dry or wet solids removal unit 13 to at least partially remove ash in the raw synthesis gas.
- a dry or wet solids removal unit 13 is known to those of ordinary skill in the art, it is not further discussed here.
- the ash is removed from the solids removal unit via line 24.
- the raw synthesis gas may be fed via line 14 to a wet gas scrubber 15 and subsequently via line 16 to battery limits.
- the residual syngas can be used for several applications like power generation, production of H2, fertilizer, Fischer Tropsch liquids and other chemicals.
- Biomass i n mixture 0% 10% 20% 30%
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Combustion & Propulsion (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Processing Of Solid Wastes (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
A process for controlling the carbon conversion of a gasifier fuelled with a carbonaceous feedstock by mixing in biomass, the process comprising the steps of (a) pressurizing the biomass and carbonaceous feedstock; (b) introducing the biomass and carbonaceous feedstock into the gasification reactor vessel; (c) partially oxidizing the carbonaceous feedstock/biomass with a molecular oxygen-comprising gas to obtain a synthesis gas comprising carbon monoxide and hydrogen; (d) measuring the C02 content of the syngas and comparing with a pre-determined value range; (e) adjusting the biomass/carbonaceous feedstock ratio by changing the biomass feed rate; wherein said biomass and carbonaceous feedstock comprises from 10 wt% to 50 wt% of biomass and wherein the level of biomass is adjusted within this range to control the carbon conversion.
Description
- -
PROCESS FOR PRODUCING SYNTHESIS GAS
The present invention relates to a process for producing synthesis gas stream from a carbonaceous feedstock, which process includes biomass fuel as a means to control the carbon conversion at a given gasification temperature in a gasification process.
WO 03/012013 describes a process for the incomplete combustion of domestic waste to produce syngas. The process as described may also include controlling the temperature in various parts of the reaction space by controlling the temperature of the oxygen-containing gas fed thereto, controlling the rate of feed of the waste and the resulting ratio of the waste feed to the oxygen- containing gas feed, and thermally insulating the reation space .
JP2002194363 describes a method for the pressurized entrained bed gasification of coal, by which biomass can be used to efficiently lower high heat generated by gasification of the coal, thereby reducing the occurrence of problems with the accumulation and fusion of ash on the operation of a pressurized entrained bed gasification furnace. The method is characterized by introducing coal particles into the lower portion of the pressurized entrained bed gasification furnace to produce the high temperature coal gas, introducing a biomass fuel into the upper portion to bring into contact with the high
temperature coal gas and gasifying the biomass fuel.
Thereby, the height of an exhaust heat recovery boiler of the gasification process can be controlled.
In the present invention a carbonaceous feedstock such as coal may be mixed with biomass prior to the mixture being introduced into the burner section of the
- - gasifier. The mixing of biomass with the coal in such a manner helps to ensure synergy between the oxygen rich biomass and oxygen lean carbonaceous feedstocks. Due to the high oxygen content in the biomass feedstock, the requirement of a moderator gas to obtain full conversion of the carbonaceous feedstock at a given gasification temperature is reduced and can even be eliminated at sufficient high fractions of biomass in the coal/biomass mixture. As moderator gas steam or carbon dioxide or a combination thereof is typically used.
An object of the present invention is to provide a simplified, energy efficient and renewable means of controlling the carbonaceous feedstock conversion by mixing in a biomass fuel. Biomass in general has a high oxygen content and can provide part of the oxygen
required for full conversion of the carbonaceous
feedstock, which in turn reduces the requirement of a moderator gas, such as steam. A certain minimum biomass fraction in the biomass/carbonaceous feedstock mixture is required to eliminate the steam. This fraction is
determined by the ultimate composition of the
lignocellulosic biomass and carbonaceous feedstock. A typical minimum fraction to get complete carbon
conversion is 10-30% of biomass by weight in the
carbonaceous feedstock/biomass mixture; however, any fraction between 10% to 50% may be used.
The above object is achieved with the following process .
A process for controlling the carbon conversion of a gasifier fuelled with a carbonaceous feedstock by mixing in biomass, the process comprising the steps of
(a) pressurizing the biomass and carbonaceous feedstock;
- -
(b) introducing the biomass and carbonaceous feedstock into the gasification reactor vessel;
(c) partially oxidizing the carbonaceous
feedstock/biomass with a molecular oxygen-comprising gas to obtain a synthesis gas comprising carbon monoxide and hydrogen;
(d) measuring the C02 content of the syngas and
comparing with a pre-determined value range;
(e) adjusting the biomass/carbonaceous feedstock ratio by changing the biomass feed rate;
wherein said gasifier feed comprises from a minimum of 10 wt% to 50 wt%, preferably 10 wt% to 30 wt% of biomass and wherein the level of biomass may adjusted within this range as needed to control the carbon conversion and reduce or eliminate the moderator gas demand. The
synthesis gas produced by this process may also contain water, hydrogen sulphide and carbon dioxide.
Applicant found that by mixing 10 wt% to 50 wt%, preferably 10 wt% to 30 wt% biomass with the carbonaceous feedstock, the temperature in the gasifier can be
controlled using the oxygen/carbonaceous fuel ratio and the carbon conversion can be controlled using the
biomass/carbonaceous fuel ratio, thereby simplifying process control. The incorporation of biomass as
described has the additional beneficial effects of saving on steam and boiler feed water consumption and also reduces the overall carbon footprint of the gasifier.
The invention will be described in more detail below .
In step (a) pressurization may be accomplished by a lock hopper system or (solids) pumps. A lock hopper system is generally used to pressurize dry and solid feedstocks. A pump can be used to pressurize liquid or
- - slurry (mixture of solids and liquid) feedstocks. A solids pump can also be applied to pressurize solid feedstocks .
In step (b) pulverized or liquid/slurry biomass can be mixed with the carbonaceous feed or fed separately to the gasifier. A separate feedline for the biomass to the gasification reactor is preferred as this will reduce the response time on a step change from the carbon conversion controller significantly. Mixing of the biomass with the carbonaceous feed can be done at several locations in the fuel preparation and pressurization section.
In step (c) any type of coal or oil burner
configurations can be used. When the biomass is supplied separately to the gasification reactor then the biomass may also be introduced through a nozzle in the burner area of the gasification reactor. The oxygen for the partial oxidation of the biomass will then need to be supplied via the carbonaceous fuel burner.
In step (c) the carbonaceous/biomass feedstock is subjected to partial oxidation with a molecular oxygen comprising gas. The partial oxidation is preferably performed at a temperature of between 1000 and 1800 °C and more preferably at a temperature between 1200 and 1800 °C. The pressure at which partial oxidation is performed is preferably between 0.3 and 12 MPa and preferably between 3 and 10 MPa. When an ash containing feedstock is used the temperature conditions are so chosen that a slag layer will form on the interior of the reactor vessel in which the partial oxidation takes place.
In step (d) the C02 content is preferably measured in cleaned and cold syngas, for example downstream of the wet scrubber. A fast measurement is preferred to minimize
- - the time between a step change in C02 concentration and the control action. An infrared based analyser is an example of such a fast measurement device.
In step (d) the C02 content of the syngas is
compared with a pre-defined value. In step (e) a
controller will subsequently adjust the biomass/coal ratio by preferably changing the set-point of the biomass feed rate controller.
The carbonaceous feedstock is preferably coal, as for example anthracite, brown coal, bitumous coal, and sub- bitumous coal. Examples of alternative carbonaceous feedstocks are petroleum coke, peat and heavy residues as extracted from tar sands or the asphalt fraction as separated from said residues in a de-asphalting process. Residues from refineries such as residual oil fractions boiling above 360 °C, directly derived from crude oil, or from oil conversion processes such as thermal cracking, catalytic cracking, hydrocracking etc may also be used as the carbonaceous feedstock.
Any biomass derived feedstocks containing low
moisture content of typically lower than 20 wt% and which can be ground to particles with sizes between 10 and 1000 micron are suitable solid biomass feedstocks comprising the 10 wt% to 50 wt% biomass component of the
carbonaceous feedstock. Feedstocks obtained by
torrefaction of a biomass source are suitable as well and are preferred at higher biomass fractions in the mixture. Torrefaction is preferably combined with a compression or pelletization step in order to make the biomass feed more suited for a gasification process wherein the biomass feed is supplied in a so-called dry form or slurry form when torrefied particles are mixed with a carbonaceous liquid. Torrefaction of biomass source material is well
- - known and for example described in M. Pach, R. Zanzi and E. Bjornbom, Torrefied Biomass a Substitute for Wood and Charcoal. 6th Asia-Pacific International Symposium on Combustion and Energy Utilization. May 2002, Kuala Lumpur and in Bergman, P.C.A., "Torrefaction in combination with pelletisation - the TOP process", ECN Report,
ECN-C-05-073, Petten, 2005.
Another suitable solid biomass fuel in the present process is obtained by drying and slow pyrolysis of a biomass source. In slow pyrolysis processes a solid char feed component is typically obtained. Slow pyrolysis is well known and for example described In: "Pyrolysis and Other Thermal Processing" . US DOE 14-08-2007.
A suitable liquid or solid biomass feedstock for use in the present process is obtained by drying and flash pyrolysis of a biomass source. In flash pyrolysis
processes a solid char and a liquid biomass feed
component are typically obtained. Both can be used as feedstock for the gasification process. Flash pyrolysis is well known and for example described in EP-A-904335; in Dinesh Mohan, Charles U. Pittman, Jr., and Philip H. Steele. Pyrolysis of Wood/Biomass for Bio-oil: A Critical Review. Energy & Fuels 2006, 20, 848-889; and in E.
Henrich: Clean syngas from biomass by pressurised
entrained flow gasification of slurries from fast
pyrolysis. In: Synbios, the syngas route to automotive biofuels, conference held from 18-20 May 2005, Stockholm, Sweden (2005) . The present invention is also directed to embodiments wherein a so-called biomass slurry is used as feedstock. The slurry can be obtained by mixing the pyrolysis oil and char.
Suitable biomass sources are weeds or residues of the agricultural industry. Examples of suitable residue
- - products are streams generated in the palm oil industry, corn industry, bio-diesel industry, forestry industry, wood processing industry and paper industry. Certain biomass is relatively expensive—for example, wood
pellets. So, in order to keep operational costs as low as possible, less costly biomass sources are preferred, such as oil palm trunks and saw dust. However, the low
quantities of biomass needed for the replacement of the moderator steam increases the chance for the application of biomass from waste streams, which are normally cheaply available in small quantities.
The present invention now provides for a process whereby the partial oxidation of a carbonaceous feedstock is performed in an efficient manner thereby obtaining synthesis gas with a reduced carbon footprint suited for catalytic conversion reactions. An especially interesting catalytic conversion reaction is a hydrocarbon synthesis process. In a hydrocarbon synthesis process, synthesis gas is catalytically converted into hydrocarbon compounds ranging from methane to high molecular weight molecules comprising up to 200 carbon atoms, or, under particular circumstances, even more. An example of a hydrocarbon synthesis process is the Fischer-Tropsch process, described in e.g. WO 02/02489, WO 01/76736, WO 02/07882, EP 510771 and EP 450861.
Step (c) may be performed by means of various
gasification processes, such as for example the so-called moving bed process, fluid bed gasifier process or the entrained-flow gasifier process as for example described in Gasification, by Christofer Higman and Maarten van der
Burgt, 2003, Elsevier Science, Burlington MA,
Pages 85-128. Preferably an entrained-flow gasifier is used because the process can handle a large variety of
- - feedstock and because a tar-free synthesis gas is
prepared. In such a process the feedstock and oxygen are introduced into the reactor co-currently, preferably by means of a suitable burner. Examples of suitable burners and their preferred uses are described in US-A-4510874 and in US-A-4523529. The operating conditions are such that the process is operated in a slagging mode, which means that the operating temperature is above the ash melting point. Suitably the carbonaceous feedstock and the molecular oxygen comprising gas is converted to synthesis gas by providing said reactants to a burner as present in a gasification reactor at a pressure of between 3 and 10 MPa and preferably at a pressure between 4 and 8 MPa. The operating temperature is suitably between 1200 and 1800°C. The synthesis gas is preferably cooled to a temperature of below 1000°C, preferably below 500°C with either direct quenching with evaporating water, direct quenching with a methanol-water mixture, by indirect heat exchange against evaporating water or combination of such cooling steps. Slag and other molten solids are suitably discharged from the gasification reactor at the lower end of the said reactor.
A solid carbonaceous feedstock/biomass feed mixture may be provided to the burner of the entrained flow gasifier reactor as a slurry in water. Coal slurry feeding processes are for example described in EP-A- 168128. Preferably the solid carbonaceous
feedstock/biomass feedstock is provided to the burner in a gas-solids mixture comprising the solid feed in the form of a powder and a suitable carrier gas. Suitable carrier gasses are nitrogen, carbon dioxide, natural gas or synthesis gas, i.e. a mixture comprising of CO and ¾ .
The carrier gas is preferably carbon dioxide. The use of
- - this carrier gas is for example described in WO-A- 2007042562.
Figure 1 shows a preferred embodiment of the present invention .
Figure 1 schematically shows a system for producing and cleaning synthesis gas. In a gasification reactor 9 a carbonaceous feed, a biomass feed and an oxygen
containing feed are introduced. The oxygen and
carbonaceous stream are fed via lines 19 and 8
respectively. The biomass can be fed separately via line
25 to the gasification reactor 9 but can also be mixed with the carbonaceous stream in the feeding and
pressurization section 7 via line 5. The carbonaceous stream 8 and biomass stream 25 are at least partially oxidised in the gasification reactor 9, thereby obtaining a raw synthesis gas 10 and a slag. To this end usually several burners (not shown) are present in the
gasification reactor 9. The biomass stream 25 can also be introduced in the gasification reactor 9 via nozzles in the burner area of gasification reactor, for example at burner level. Then the oxygen for the partial oxidation of the biomass will be added to the burner oxygen of the carbonaceous stream 8.
The carbon conversion of the gasifier is controlled with controller 18. Input for the carbon conversion controller is the measured C02 content of the syngas 16 downstream of the wet scrubber 15 with the C02 analyser 17. As soon as the C02 content drops below a pre¬ determined value than the biomass/coal ratio needs to be increased by changing the biomass feed 3 and increasing the flow rate of line 5 or 25. As soon as the C02
concentration exceeds a maximum pre-determined value, then the biomass/coal ratio can be reduced by changing
- - the biomass feed 3 and decreasing the flow rate of line 4 or 25. The C02 analyser and benefits for controlling the steam and oxygen to carbon (O/C) ratio are described in WO2008125556A1 and W0200768684A2.
An advantage for the use of biomass to control the carbon conversion is that a C02 neutral feedstock is used, which reduces the C02 footprint of the plant. In addition this application reduces the high pressure steam and high quality boiler feed water requirements for the gasification island.
The produced raw synthesis gas is fed via line 10 to a cooling section 11; herein the raw synthesis gas is usually cooled to about 200-400 °C. The cooling section 11 may be an indirect heat exchanger or a quench vessel. In case of a quench vessel liquid water is preferably injected via line 23 into a synthesis gas stream. Liquid water is preferably injected in the form of a mist.
The cooling section 11 can be integrated in the gasification reactor pressure vessel at the bottom of the reactor or installed as a separate vessel. When the syngas and slag both exit at the bottom of the
gasification reactor then the cooling section 11 is integrated in the pressure vessel and both the syngas and fly ash and slag will enter the cooling section. When the syngas leaves the gasification reactor 9 at the top and slag at the bottom then only syngas with fly ash will enter the cooling section that is installed as separate section downstream of the reactor.
As shown in the embodiment of Figure 1, the raw synthesis gas leaving the cooling section 10 is further processed. To this end, it is fed via line 12 into a dry or wet solids removal unit 13 to at least partially remove ash in the raw synthesis gas. As the solids
- - removal unit 13 is known to those of ordinary skill in the art, it is not further discussed here. The ash is removed from the solids removal unit via line 24. After the solids removal unit 13 the raw synthesis gas may be fed via line 14 to a wet gas scrubber 15 and subsequently via line 16 to battery limits. After further syngas treating, the residual syngas can be used for several applications like power generation, production of H2, fertilizer, Fischer Tropsch liquids and other chemicals.
The reduction of the moderator steam with the addition of biomass to coal was modelled using a computer simulation. For the gasification of a selected Drayton coal, approximately 76 kg steam per tonne coal will be required to obtain full carbon conversion at a
gasification temperature of 1500°C. The addition of coal with wood will gradually reduce the moderator requirement as shown in table 1. With the replacement of >25% of the coal with wood, moderator steam can be eliminated.
Table 1--Typical moderator consumption at different biomass fractions in biomass/coal mixture
Coal i n mixture 100% 90% 80% 70%
Biomass i n mixture 0% 10% 20% 30%
Gasification conditions
Tem perature °C 1500 1500 1500 1500
Pressure bara 41 41 41 41
GASIFIER INPUT
Carrier kg/s 2.7 2.7 2.7 2.7
Moderator steam kg/s 2*1 1.1 0.2 0.0
02 kg/s 22.2 21.3 20.4 19.7
Fuel kg/s 27.6 27.6 27.6 27.6
GASIFIER OUTPUT
Syngas kg/s 49.9 48.5 47.1 46.6
Slag kg/s 6.0 5.5 4.9 4.4
Claims
1. A process for controlling the carbon conversion of a gasifier fuelled with a carbonaceous feedstock by mixing in biomass, the process comprising the steps of
(a) pressurizing the biomass and carbonaceous feedstock;
(b) introducing the biomass and carbonaceous
feedstock into the gasification reactor vessel;
(c) partially oxidizing the carbonaceous
feedstock/biomass with a molecular oxygen-comprising gas to obtain a synthesis gas comprising carbon monoxide and hydrogen;
(d) measuring the C02 content of the syngas and comparing with a pre-determined value range;
(e) adjusting the biomass/carbonaceous feedstock ratio by changing the biomass feed rate;
wherein said biomass and carbonaceous feedstock comprises from 10 wt% to 50 wt% of biomass and wherein the level of biomass is adjusted within this range to control the carbon conversion.
2. Process according to claim 1, wherein the
carbonaceous feedstock and biomass are separately
introduced into the gasification reactor.
3. Process according to claim 1, wherein the
carbonaceous feedstock and biomass are introduced in the gasification reactor as a mixture.
4. Process according to any one of claims 1-3, wherein the feedstock to the gasifier comprises from 10 wt% to 30 wt% of biomass fuel.
5. Process according to any one of claims 1-4, wherein the biomass is a solid biomass as obtained by
torrefaction .
6. Process according to any of claims 1-5, wherein the biomass is a solid biomass as obtained by slow pyrolysis of a biomass source.
7. Process according to any one of claims 1-6, wherein the biomass is a solid biomass as obtained by flash pyrolysis of a biomass source.
8. Process according to claim 4, wherein the biomass is a liquid biomass as obtained by flash pyrolysis of a biomass source.
9. Process according to claim 4, wherein the biomass is a slurry biomass consisting of a mixture of pyrolysis oil and char as obtained by flash pyrolysis of a biomass source .
10. Process according to any one of claims 1-9 wherein the carbonaceous feedstock is coal.
11. Process according to any one of claims 1-9 wherein the carbonaceous feedstock is oil residue.
12. Process according to any one of claims 1-11, wherein in step (c) the carbonaceous feedstock/biomass fuel mixture and the molecular oxygen comprising gas are converted to synthesis gas by providing said reactants to a burner as present in a gasification reactor at a pressure of between 1 and 10 MPa.
13. Process according to any one of claims 1-12, wherein in step (d) the C02 content is measured using an infrared based analyser.
14. Process according to any one of claims 1-13,
wherein, in step (e) a controller will adjust the
biomass/coal ratio by changing the set-point of a biomass feed rate controller.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP11799698.3A EP2655566A1 (en) | 2010-12-21 | 2011-12-20 | Process for producing synthesis gas |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP10196098 | 2010-12-21 | ||
| EP11799698.3A EP2655566A1 (en) | 2010-12-21 | 2011-12-20 | Process for producing synthesis gas |
| PCT/EP2011/073417 WO2012084953A1 (en) | 2010-12-21 | 2011-12-20 | Process for producing synthesis gas |
Publications (1)
| Publication Number | Publication Date |
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| EP2655566A1 true EP2655566A1 (en) | 2013-10-30 |
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| EP11799698.3A Withdrawn EP2655566A1 (en) | 2010-12-21 | 2011-12-20 | Process for producing synthesis gas |
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| US (1) | US20130326954A1 (en) |
| EP (1) | EP2655566A1 (en) |
| CN (1) | CN103314083B (en) |
| AU (1) | AU2011347466B2 (en) |
| MY (1) | MY165497A (en) |
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| CN103838265B (en) * | 2014-03-07 | 2016-09-28 | 西北化工研究院 | A kind of in the control system producing synthesis gas time control hydrogen and carbon monoxide ratio |
| WO2016018836A1 (en) * | 2014-07-28 | 2016-02-04 | Sustainable Waste Power Systems, Inc. | Method of synthetic fuel gas production |
| CN108905962A (en) * | 2018-06-26 | 2018-11-30 | 江苏新亿源环保科技有限公司 | A kind of preparation method of biomass carbon adsorbent material |
| WO2025026747A1 (en) * | 2023-07-31 | 2025-02-06 | Basf Se | System and method for controlling the biogenic carbon content during manufacture of a chemical product |
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| GB8307519D0 (en) | 1983-03-18 | 1983-04-27 | Shell Int Research | Burner |
| US4581899A (en) | 1984-07-09 | 1986-04-15 | Texaco Inc. | Synthesis gas generation with prevention of deposit formation in exit lines |
| CA2038773C (en) | 1990-04-04 | 1999-06-08 | Kym B. Arcuri | Slurry fischer-tropsch process with co/ti02 catalyst |
| GB9108663D0 (en) | 1991-04-23 | 1991-06-12 | Shell Int Research | Process for the preparation of a catalyst or catalyst precursor |
| BR9709327A (en) | 1996-05-20 | 2000-05-02 | Rti Resource Transforms Intern | Liquefaction of biomaterials by means of energy efficient thermolysis |
| MY136454A (en) | 2000-04-07 | 2008-10-31 | Shell Int Research | A process for producing hydrocarbons, and a catalyst suitable for use in the process |
| ES2227249T3 (en) | 2000-07-03 | 2005-04-01 | Shell Internationale Research Maatschappij B.V. | CATALYST AND HYDROCARBON PREPARATION PROCEDURE. |
| DE60102246T2 (en) | 2000-07-24 | 2004-07-29 | Shell Internationale Research Maatschappij B.V. | SHELL METAL CATALYST AND A PRECURSOR THEREFOR, METHOD FOR THE PRODUCTION AND USE THEREOF OF THIS CATALYST |
| JP4072612B2 (en) | 2000-12-27 | 2008-04-09 | 独立行政法人産業技術総合研究所 | Pressurized spouted bed gasification method of coal using biomass |
| US20030046868A1 (en) * | 2001-03-12 | 2003-03-13 | Lewis Frederic Michael | Generation of an ultra-superheated steam composition and gasification therewith |
| IL144718A (en) | 2001-08-02 | 2006-12-10 | T G E Tech Ltd | Method and apparatus for the treatment of domestic waste |
| US8118894B2 (en) * | 2006-07-18 | 2012-02-21 | The Regents Of The University Of California | Commingled coal and biomass slurries |
| WO2006003615A1 (en) * | 2004-06-29 | 2006-01-12 | Sasol Technology (Proprietary) Limited | Particulate fuel |
| EP1896553A4 (en) * | 2005-06-03 | 2010-09-01 | Plascoenergy Ip Holdings Slb | SYSTEM FOR CONVERTING CARBON FEEDSTOCKS TO A GAS OF A SPECIFIC COMPOSITION |
| US20070225382A1 (en) | 2005-10-14 | 2007-09-27 | Van Den Berg Robert E | Method for producing synthesis gas or a hydrocarbon product |
| BRPI0619877B1 (en) | 2005-12-14 | 2016-07-05 | Shell Int Research | method of producing synthesis gas by partial oxidation of a carbonaceous stream, and suitable system for carrying out the same |
| CN100410352C (en) * | 2006-04-21 | 2008-08-13 | 江苏大学 | A gasification process and device for co-gasification of biomass and coal |
| AP2008004698A0 (en) * | 2006-06-05 | 2008-12-31 | Plascoenergy Ip Holdings S L | A gasifier comprising vertically successive processing regions |
| EP2134818B1 (en) | 2007-04-11 | 2017-03-29 | Shell Internationale Research Maatschappij B.V. | Process for operating a partial oxidation process of a solid carbonaceous feed |
| US8574329B2 (en) * | 2008-12-11 | 2013-11-05 | General Electric Company | Method of operating a gasifier |
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2011
- 2011-12-20 CN CN201180065454.1A patent/CN103314083B/en active Active
- 2011-12-20 EP EP11799698.3A patent/EP2655566A1/en not_active Withdrawn
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- 2011-12-20 WO PCT/EP2011/073417 patent/WO2012084953A1/en not_active Ceased
- 2011-12-20 US US13/995,970 patent/US20130326954A1/en not_active Abandoned
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Also Published As
| Publication number | Publication date |
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| WO2012084953A1 (en) | 2012-06-28 |
| CN103314083A (en) | 2013-09-18 |
| US20130326954A1 (en) | 2013-12-12 |
| MY165497A (en) | 2018-03-27 |
| AU2011347466B2 (en) | 2015-07-16 |
| ZA201304552B (en) | 2014-03-26 |
| CN103314083B (en) | 2015-07-22 |
| AU2011347466A1 (en) | 2013-07-11 |
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