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WO2015116385A1 - Procédé de conversion de biomasse en utilisant un système de catalyseur multifonctionnel - Google Patents

Procédé de conversion de biomasse en utilisant un système de catalyseur multifonctionnel Download PDF

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Publication number
WO2015116385A1
WO2015116385A1 PCT/US2015/011421 US2015011421W WO2015116385A1 WO 2015116385 A1 WO2015116385 A1 WO 2015116385A1 US 2015011421 W US2015011421 W US 2015011421W WO 2015116385 A1 WO2015116385 A1 WO 2015116385A1
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Prior art keywords
component
catalyst
fed
reactor
stage
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English (en)
Inventor
Maria Magdalena Ramirez Corredores
Ling Zhou
Rocio BANDA
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Inaeris Technologies LLC
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Kior Inc
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    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G1/00—Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal
    • C10G1/08—Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal with moving catalysts
    • C10G1/086—Characterised by the catalyst used
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J21/00—Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
    • B01J21/02—Boron or aluminium; Oxides or hydroxides thereof
    • B01J21/04—Alumina
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J21/00—Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
    • B01J21/10—Magnesium; Oxides or hydroxides thereof
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/16—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
    • B01J23/24—Chromium, molybdenum or tungsten
    • B01J23/28—Molybdenum
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
    • B01J27/20—Carbon compounds
    • B01J27/22—Carbides
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J29/00—Catalysts comprising molecular sieves
    • B01J29/04—Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites
    • B01J29/06—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
    • B01J29/08—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the faujasite type, e.g. type X or Y
    • B01J29/084—Y-type faujasite
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J29/00—Catalysts comprising molecular sieves
    • B01J29/04—Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites
    • B01J29/06—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
    • B01J29/40—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the pentasil type, e.g. types ZSM-5, ZSM-8 or ZSM-11, as exemplified by patent documents US3702886, GB1334243 and US3709979, respectively
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J29/00—Catalysts comprising molecular sieves
    • B01J29/04—Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites
    • B01J29/06—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
    • B01J29/80—Mixtures of different zeolites
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G1/00—Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal
    • C10G1/08—Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal with moving catalysts
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
    • C10G2300/10—Feedstock materials
    • C10G2300/1011—Biomass
    • 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
    • Y02P30/00—Technologies relating to oil refining and petrochemical industry
    • Y02P30/20—Technologies relating to oil refining and petrochemical industry using bio-feedstock

Definitions

  • the disclosure relates to a method of converting biomass to hydrocarbons using a multi-functional catalyst.
  • Renewable energy sources are a substitute for fossil fuels and provide a means of reducing dependence on petroleum oil.
  • Renewable fuels include biofuels which may be produced by subjecting a biomass, such as a lignocellulosic biomass, to catalytic thermolysis processes, such as pyrolysis. This results in the conversion of the biomass into hydrocarbon containing feedstreams which are then used to produce biofuels.
  • a biomass such as a lignocellulosic biomass
  • catalytic thermolysis processes such as pyrolysis.
  • the lignocellulosic biomass is deoxygenated and depolymerized. Dehydration and dehydroxylation of the biomass are typically the principal reactions occurring during pyrolysis.
  • carbonyl linkages within the biomass may be broken down into carbon monoxide by decarbonylation.
  • Decarbonylation which typically increases in catalytic pyrolysis, decreases the liquid yield by removing carbon bearing molecules with gaseous streams.
  • a water-gas shift (WGS) reaction might also occur during deoxygenation of the biomass wherein carbon dioxide and hydrogen are produced from the reaction of carbon monoxide and water, depending on catalyst and reaction conditions.
  • a mono-functional catalyst e.g., an acid catalyst
  • different mono-functional catalysts have been used for various purposes, such as to modulate cracking and enhance decarboxylation to maximize carbon dioxide (e.g., bases).
  • the use of a mono-functional catalyst to tackle the complexity of pyrolysis decreases the efficiency of conversion of the biomass to hydrocarbons and shortens the life cycle of any catalyst used within the biomass conversion unit. While bi-functional catalysts have been explored, a method which enhances the processability of biomass feedstocks with multifunctional catalysts has not been reported.
  • the disclosure relates to a process of converting solid biomass to hydrocarbons by feeding into a biomass conversion unit at least a portion of a regenerated multi-functional catalyst.
  • the regenerated multi-functional catalyst contains an acidic component, a basic component and a metallic component.
  • the biomass is treated within the biomass conversion unit in at least two stages wherein at least a fresh portion of one component of the regenerated multi-functional catalyst is fed into each of the stages.
  • the disclosure relates to a process of converting solid biomass to hydrocarbons in a two stage process.
  • the process is conducted in the presence of at least a portion of a first regenerated catalyst and at least a portion of a second regenerated catalyst wherein the first regenerated catalyst or the second regenerated catalyst is a monofunctional catalyst and the other is a bifunctional catalyst.
  • the combination of the monofunctional catalyst and the bifunctional catalyst contains an acidic component, a basic component and a metallic component.
  • the bifunctional catalyst contains two of the components and the monofunctional catalyst contains the remaining component.
  • a first stage reactor has a first solids separator and a first regeneration unit and a second stage reactor has a second solids separator and a second regeneration unit.
  • the solid biomass is subjected to catalytic pyrolysis in the first stage reactor unit.
  • Spent catalyst and vapors are separated from the pyrolyzed biomass in the first solids separator.
  • the separated vapor is then fed into the second stage reactor.
  • the spent catalyst is fed into the first regeneration unit to render the first regenerated catalyst.
  • the vapor phase is subjected to a second catalytic pyrolysis step in the second stage reactor.
  • Spent catalyst separated from the pyrolyzed vapor phase in the second stage reactor is fed into the second regeneration unit to render the second regenerated catalyst.
  • At least a portion of the first regenerated catalyst is fed into the first stage reactor and at least a portion of the second regenerated catalyst is fed into the second stage reactor.
  • At least a fresh portion of one component of the regenerated multifunctional catalyst is fed into each of the stages.
  • a process of converting solid biomass to hydrocarbons in at least two stages is disclosed.
  • the biomass is subjected to pyrolysis in a first stage reactor in the absence of a catalyst.
  • Vapors and solids are separated from the pyrolyzed biomass.
  • the separated vapor is fed into a second reactor.
  • the separated vapor is converted into hydrocarbons in the presence of a regenerated multi-functional catalyst in the second reactor.
  • At least a fresh portion of the multi-functional catalyst is fed into the second stage.
  • the multi-functional catalyst contains an acid component, a basic component and a metallic material.
  • a process of converting solid biomass to hydrocarbons wherein the biomass is first pyrolyzed in a biomass conversion unit in the absence of a catalyst. Solids and vapors are separated from the pyrolyzed product. At least a portion of a regenerated multifunctional catalyst is fed into a second reactor. The regenerated catalyst contains an acidic component, a basic component and a metallic component. The separated vapor is then pyrolyzed in the presence of at least a portion of the regenerated catalyst.
  • a process of converting solid biomass to hydrocarbons wherein a regenerated multi-functional catalyst comprising an acidic component, a basic component and a metallic component is fed into a biomass conversion unit. The biomass is then pyrolyzed in the biomass conversion unit.
  • the present disclosure includes features and advantages which are believed to enable it to advance the conversion of biomass into hydrocarbons. Characteristics and advantages of the present disclosure described above and additional features and benefits will be readily apparent to those skilled in the art upon consideration of the following detailed description of various embodiments and referring to the accompanying drawings.
  • FIG. 1 illustrates the process of converting solid biomass to hydrocarbons by feeding a regenerated multi-functional catalyst into a biomass conversion unit.
  • FIG. 2 illustrates a process of converting solid biomass to hydrocarbons in two stages wherein in the first stage a biomass feedstream is pyrolyzed in a first reactor in the absence of a catalyst and in the second stage a vapor phase (separated from the biomass in the first reactor) is subjected to pyrolysis in a second reactor in the presence of a regenerated multi-functional catalyst.
  • FIGs. 3 A, 3B and 3C illustrate a process of converting solid biomass to hydrocarbons by feeding a regenerated multi-functional catalyst into a biomass conversion unit in two stages.
  • a single component of a multi-functional catalyst is fed into the first stage of the biomass conversion unit and two components of the multifunctional catalyst are fed into the second stage.
  • FIGs. 4A, 4B and 4C illustrate a process of converting solid biomass to hydrocarbons by feeding a regenerated multi-functional catalyst into a biomass conversion unit in two stages. Two components of the multi-functional catalyst are fed into the first stage of the biomass conversion unit and one component of the multifunctional catalyst is fed into the second stage.
  • FIGs. 5A, 5B and 5C illustrate a process of converting solid biomass to hydrocarbons by feeding a regenerated multi-functional catalyst into a biomass conversion unit in two stages.
  • a single component of a multi-functional catalyst is fed into a first reactor and two components of the multi-functional catalyst are fed into a second reactor.
  • Both reactors have a solids separator and a catalyst regenerator.
  • FIGs. 6A, 6B and 6C illustrate a process of converting solid biomass to hydrocarbons by feeding a regenerated multi-functional catalyst into a biomass conversion unit in two stages. Two components of a multi-functional catalyst are fed into a first reactor and one component of the multi-functional catalyst is fed into a second reactor. Both reactors have a solids separator and a catalyst regenerator.
  • FIG. 7 is a representative reactor system which may be used to practice the process disclosed herein as illustrated in Example 1.
  • FIGs. 8A, 8B, 8C and 8D illustrate product distributions which may result from the disclosed process.
  • Preferred embodiments of the present disclosure thus offer advantages over the prior art and are well adapted to carry out one or more of the objects of this disclosure.
  • the present disclosure does not require each of the components and acts described above and is in no way limited to the above-described embodiments or methods of operation. Any one or more of the above components, features and processes may be employed in any suitable configuration without inclusion of other such components, features and processes.
  • the present disclosure includes additional features, capabilities, functions, methods, uses and applications that have not been specifically addressed herein but are, or will become, apparent from the description herein, the appended drawings and claims.
  • the method disclosed herein uses a multi-functional catalyst.
  • Such catalysts provide greater versatility than those mono-functional catalysts typically used to convert biomass into renewable fuels.
  • Multi-functional catalysts are further capable of maximizing liquid yield of produced hydrocarbons in a more cost effective manner.
  • the multi-functional catalyst used may have an acidic component, a basic component and a metallic component.
  • the biomass Prior to treatment of the biomass with the multi-functional catalyst, the biomass may be subjected to "thermal pyrolysis" wherein the feedstock is heated in the substantial absence of a catalyst in an atmosphere that is substantially free of oxygen.
  • the atmosphere may be an inert gas, such as nitrogen.
  • the atmosphere can comprise a reactive gas, such as hydrogen, carbon monoxide, steam, or a combination thereof.
  • Treatment of the biomass with the multi-functional catalyst may occur in one or more stages.
  • the multi-functional catalyst may be regenerated in one or more stages.
  • the first stage and the second stage may correspond to the lower and the upper zone or section of the reactor. In such instances, the two zones of the reactor may have different geometries. For example, the lower zone of the reactor may have a frustrum geometry and the second zone a cylindrical geometry.
  • the two stages or zones of the reactor may have different diameters.
  • the particulate solid biomass material is thermally pyrolyzed, to form primary reaction products and in the second stage primary reaction products may be catalytically converted to secondary reaction products.
  • the first stage and second stage of the single reactor are typically in fluid communication.
  • different components of the catalyst may be introduced into different reactors.
  • different regenerated components of the catalyst are fed back into different reactors.
  • two or more of the components of the catalyst may be introduced into a first reactor (as one stage) and one or more other components of the catalyst may be introduced into a second reactor (as another stage).
  • the components introduced into the first reactor may then be regenerated and fed back into the first reactor.
  • the components introduced into the second reactor may be regenerated and fed back into the second reactor.
  • each stage has a reactor for one or more of the components of the catalyst.
  • each of the multiple stages may have a single reactor for a single component such that each component of the multi-functional catalyst is introduced in a separate reactor. Thus, when regenerated, the single component may be fed back into its respective reactor.
  • the process is conducted in at least two reactors.
  • the process employs two reactors wherein at least one of the components is introduced into one reactor (a first stage) and the remaining components are introduced into a second reactor (a second stage).
  • solid particulate biomass material is converted thermally pyrolyzed in the first stage reactor to form primary reaction products and in the second stage reactor at least part of the primary reaction products are catalytically converted to secondary reaction products.
  • the first stage and second stage reactors are in fluid communication.
  • the second stage reactor is positioned above the first stage reactor.
  • the presence of the acidic component in the multi-functional catalyst preferred for use in the method disclosed herein accelerates deoxygenation of low molecular oxygenates which are produced in high amounts during the conversion of biomass.
  • oxygenates are alcohols, aldehydes, ketones, carboxylic acids, diols, ethers, esters, and the like.
  • Those having an isolated carbonyl group include aldehydes and ketones like acetaldehyde, methyl vinyl ketone and ethyl vinyl ketone.
  • the acidic component of the multi-functional catalyst is zeolite ZSM-5.
  • the presence of zeolite ZSM-5 promotes oligocyclization and/or aromatization of the bio-oil and/or pyrolysis oil compounds.
  • zeolite enables production of higher molecular weight hydrocarbons versus the low molecular weight (generally less than C5) in bio-oil and/or pyrolysis oil produced during pyrolysis of a biomass in a biomass conversion unit.
  • amount of zeolite ZSM-5 in the multi-functional catalyst disclosed herein may be from about 5 to about 40 wt. %. (As used herein, the wt.
  • % of a component of the multi-functional catalyst refers to the amount of the component based on all of the components in all of the stages.)
  • the amount of zeolite ZSM-5 based on the weight percent of all of the components of the multi-functional catalyst within the stages, is from about 5 to about 40 wt. %.
  • the multi-functional catalyst disclosed herein may also include zeolite USY.
  • Zeolite USY promotes cracking of the biomass monomers, dimers and/or small oligomers.
  • the amount of zeolite USY in the multi-functional catalyst is from about 5 to about 40 wt. %.
  • the weight ratio of Si:Al in zeolite USY is from about 5 to about 200, more typically from about 20 to about 100.
  • L-zeolite may also be included with zeolite ZSM-5 and zeolite USY in the preferred multi-functional catalyst.
  • the amount of L-zeolite in the multi-functional catalyst is less than about 20 wt. %.
  • L-zeolite may be used to promote aromatization of hydrocarbons produced during pyrolysis.
  • the ZSM-5 zeolite, zeolite USY and, optional, L-zeolite in the preferred multi-functional catalyst are included in their acid form and thus provide an acidic functionality to the multi-functional catalyst.
  • the presence of the metallic component in the multi-functional catalyst promotes the WGS reaction producing hydrogen in-situ and consequently minimizing hydrogen transfer reaction from the organic solid to the vapors.
  • Reactants for the WGS reaction may be produced during catalytic pyrolysis, deoxygenation and cracking of the biomass. For instance, deoxygenation via decarbonylation and dehydroxylation produces carbon monoxide and water, respectively.
  • the metallic component enhances dry reforming (DR) reaction between hydrocarbon moieties and carbon dioxide to increase further the hydrogen content of the gas phase and suppress even more the hydrogen transfer from the organic solid to the vapors.
  • Suitable metallic components of the multi-functional catalyst include copper, nickel, chromium, tungsten, molybdenum, a metal carbide, a metal nitride, a metal sulfide or a mixture thereof.
  • Suitable metal carbides include chromium carbide, molybdenum carbide and tungsten carbide as well as mixtures thereof. In a preferred embodiment, the metal carbide is molybdenum carbide.
  • the metallic component of the multi-functional catalyst is copper, nickel or a carbide of molybdenum and mixtures thereof.
  • the metallic component is a blend of copper and molybdenum carbide or a blend of nickel and molybdenum carbide.
  • the basic component of the multi-functional catalyst typically enables decarboxylation of the biomass and thus assists in the removal of oxygen from the biomass.
  • the material providing the basic functionality to the multi-functional catalyst is preferably an alkaline-exchanged zeolite, an alkaline earth-exchanged zeolite, basic zeolite, an alkaline earth metal oxide, cerium oxide, zirconium oxide, titanium dioxide, mixed oxides of alkaline earth metal oxides and combinations thereof and mixed oxides selected from the group of magnesia-alumina, magnesia-silica, titania-alumina, titania- silica, ceria-alumina, ceria-silica, zirconia-alumina, zirconia-silica and mixtures thereof and wherein the exchanged zeolite has from about 40 to about 75% of exchanged cationic sites.
  • the exchanged zeolite has 50% exchanged cationic sites.
  • the basic material is an alkaline earth metal oxide, cerium oxide, zirconium oxide, titanium dioxide, mixed oxide of an alkaline earth metal oxide and combinations thereof or a mixed oxide selected from the group of magnesia-alumina, magnesia-silica, titania-alumina, titania-silica, ceria-alumina, ceria-silica, zirconia- alumina, zirconia-silica and mixtures thereof
  • the basic material may further serve to form a support or a matrix for the other components of the multi-functional catalyst.
  • the basic material may be the support for the metallic component.
  • the multi-functional catalyst defined herein may also include a binder for agglomerating the different functional entities of the catalyst and facilitating molding and/or shaping of the components of the catalyst.
  • the binder may present in one or more of the stages.
  • Suitable binders include clay -based binders (such as kaolin-based binder), alumina based binders (such as aluminum chlorohydrol and aluminum nitrohydrol), silica based binders (such as silicic acid, polysilicic acid, silica gel and colloidal silica) as well as combinations of any of such binders.
  • the binder is kaolin-based.
  • the amount of binder in the multi-functional catalyst is typically less than 50 wt. %, more typically less than 30 wt. %.
  • the multi-functional catalyst for use in the methods disclosed herein may also include a promoter.
  • Suitable promoters include phosphates, silica, alumina and metallic promoters and mixtures thereof.
  • phosphate is typically used to promote the catalytic effect of the acid component and to enhance the binding capabilities of the binding materials and is present in the stage where the acid component is present.
  • Silica and/or alumina are typically used to promote the catalytic effect of the basic material and is present in the stage where the basic material is present.
  • a metallic promoter is typically used to impart either a bi-metallic functionality or to stabilize the metallic component and thus enhance the performance of the metal component of the multi-functional catalyst.
  • the metallic promoter is typically present in the stage where the metallic component is present.
  • the multi-functional catalyst for use in the methods defined herein may contain from about 5 to about 40 wt. % zeolite ZSM-5; from about 5 to about 30 wt. % zeolite USY; from about 3 to about 15 wt. % of metallic material; and from about 5 to about 40 wt. % of basic material; the balance being the binder.
  • biomasses contain carboxylic groups and ester-type bonds that can be decarboxylated, providing a suitable catalyst functionality is included. Said functionality is provided by the basic material component of the multi-functional catalyst.
  • the enhanced formation of carbon dioxide from the decarboxylation reaction of biomass moieties further drives the dry reforming reactions promoted by the metallic component of the multifunctional catalyst.
  • the biomass may be pre -treated with at least one component of the catalyst system.
  • a pretreatment step can comprise impregnating a cellulosic biomass with a solution of a component of the catalyst system.
  • pretreatment is carried out with one or more solid components of the multi-functional catalyst by mechanically treating the biomass in the presence of the catalyst component in particulate form.
  • the mechanical treatment can comprise milling, grinding, kneading, or a combination thereof.
  • the biomass initially introduced into the reactor(s) may be in a solid or finely divided form or may be a liquid.
  • the water soluble content of the biomass is no greater than about 7 volume percent.
  • the biomass particles can be fibrous biomass materials comprising cellulose.
  • suitable cellulose-containing materials include algae, paper waste, and/or cotton linters.
  • the biomass particles can comprise a lignocellulosic material.
  • suitable lignocellulosic materials include forestry waste such as wood chips, saw dust, pulping waste, and tree branches; agricultural waste such as corn stover, wheat straw, and bagasse; and/or energy crops such as eucalyptus, switch grass, miscanthus, coppice and fast-growing woods, such as willow and poplar.
  • the biomass may be subjected to any of a variety of conversion conditions.
  • conversion conditions include those of fast pyrolysis, slow pyrolysis, liquefaction, catalytic gasification, thermocatalytic conversion, etc.
  • the reactors are a fluidized bed reactor, a cyclone reactor, an ablative reactor, an auger reactor, a riser reactor, a trickle bed configuration, another bed regimen or a combination thereof.
  • the reactors are typically fluid bed reactors wherein at least part of the thermo catalyst might be used as a heat carrier.
  • the components of the catalyst should have a shape and size to be readily fluidized. Preferred are components in the form of microspheres having a particle size in the range of 20 ⁇ to 3000 ⁇ .
  • a broad range of fluidization conditions might be used when more than one stage is desired.
  • a two stage fluidized bed system might comprise two fluidized bed reactors coupled together with provisions for gas and/or materials transfer in between.
  • Feasible combinations include circulating-circulating or bubbling-circulating or bubb ling-bubbling type systems.
  • solid biomass particles may be agitated, for example, to reduce the size of particles. Agitation may be facilitated by a gas including one or more of steam, flue gas, carbon dioxide, carbon monoxide, hydrogen, and hydrocarbons such as methane.
  • the agitator further be a mill (e.g., ball or hammer mill) or kneader or mixer.
  • the reactor(s) is operated at temperatures in excess of 250°C.
  • reaction temperatures may be as high as 1,000°C.
  • the reactor is maintained at a temperature in the range of from 250°C to about 650°C, more typically preferably from 400°C to 600°C.
  • FIG. 1 illustrates a single stage process wherein multi-functional catalyst 1 10 is shown as being introduced into biomass conversion unit 1 14.
  • the biomass is thermocatalytically treated to render liquid products that spontaneously separate into an aqueous phase and an organic phase.
  • Bio-oil (which is used to produce biofuel) consists of the organic phase.
  • water may be removed during the separation.
  • the bio-oil, having the byproduct water, heavy materials and solids removed may then be introduced into a fractionator.
  • the multi-functional catalyst disclosed herein may be added as fresh catalyst to the biomass conversion unit.
  • the multi-functional catalyst may be an equilibrium catalyst ("E-cat"), also referred to as regenerated catalyst.
  • E-cat equilibrium catalyst
  • Such catalysts are produced by burning coke deposits and/or char from a spent catalyst in oxygen or an oxygen containing gas, such as air, in a catalyst regeneration unit or regenerator. All or a portion of the spent catalyst formed in the biomass conversion unit may be subjected to treatment in the regenerator.
  • Biomass conversion unit 114 may, for example, be a fluidized bed or a trickle bed configuration or another bed regimen.
  • the biomass may be converted in a single stage to hydrocarbons (including bio-oil) in the biomass conversion unit.
  • Undesirable heavy materials and solids may be separated from the pyrolyzed biomass in solids separator 124 and the solids, including spent catalyst 130, are then allowed to proceed to catalyst regeneration unit 118.
  • Suitable solid separators in the figures provided herein may be a cyclone, coalescer, gravity phase separator, liquid hydrocyclone, electrostatic desalter, etc.
  • the liquid portion 131 separated in solids separator 124 may then be further processed to render hydrocarbon distillates for use in renewable fuel production.
  • catalyst regeneration unit 118 spent catalyst 130 is regenerated. Regenerated catalyst is then introduced into biomass conversion unit 114. Solid biomass 1 12 may also be introduced with multi-functional regenerated catalyst 122 into biomass conversion unit 114 through line 120. During the process, fresh multi-functional catalyst may optionally be added into biomass conversion unit 114 in order to attain the desired activity of the catalyst within the reactor. Similarly, lower activity regenerated catalyst may optionally be removed from the catalyst regeneration unit 118 in order to attain the desired activity of the catalyst within the reactor and keep solid hold-up in the unit.
  • FIG. 2 illustrates another embodiment wherein biomass is treated in two stages.
  • biomass may be fed through line 21 1 into a first stage (pyrolysis) reactor 216.
  • undesirable heavy materials and solids may be separated from the pyrolyzed biomass in first solids separator 224.
  • first solids separator 224 typically, from about 90 to 95 weight percent of the solids are removed from the biomass in separator 224.
  • water may be removed during the separation.
  • Remaining treated biomass, enriched with heavy materials and solids including the heat carrier separated from the pyrolyzed biomass in solids separator 224 is then fed via line 226 back into first stage (pyrolysis) reactor 216.
  • the treated biomass enriched with heavy materials and produced biochar, may occasionally be removed from the separated solid stream prior to feeding the separated heat carrier via line 226 back into first stage (pyrolysis) reactor 216.
  • Untreated biomass may further be fed through line 212 into first stage reactor 216 and admixed with the solids stream from line 226.
  • the pyrolysis products are upgraded in the presence of a multi-functional catalyst.
  • the separated vapors from the pyrolyzed biomass, substantially free of solids separated in first solids separator 224 is introduced into a second stage reactor 228 through line 240.
  • the vapor may include, in addition to liquid reaction products, the lift gas and gaseous reaction products such as carbon dioxide, carbon monoxide, and relatively minor amounts of hydrogen, methane, ethylene and other light hydrocarbons.
  • Multi-functional catalyst may be fed into second stage reactor 228 via line 210.
  • the treated biomass from second stage reactor 228 may then be introduced into the second solids separator 234.
  • Solids, including spent or contaminated catalyst 230, separated in the second solids separator 234 may then be fed into the catalyst regeneration unit 218.
  • catalyst regeneration unit 2108 regenerated catalyst or E- cat is produced by burning coke deposits from spent catalyst in oxygen or an oxygen containing gas, such as air.
  • the bio-oil, having the byproduct water, heavy materials and solids removed in second solids separator 234 may be further processed.
  • the bio-oil may be introduced into a fractionator for further processing to render boiling point equivalent fractions of renewable gasoline, renewable jet fuel, renewable diesel and/or renewable fuel oil.
  • Multi-functional catalyst 222 regenerated in regeneration unit 218, may then be fed into second stage reactor 228 through line 240.
  • fresh multi-functional catalyst may optionally be added into second stage reactor 228 in order to attain desired activity of the catalyst within the reactor.
  • lower activity regenerated catalyst may optionally be removed from catalyst regeneration unit 218 in order to attain the desired activity of the catalyst within the reactor and keep solid holdup in the unit.
  • FIG. 3A a two stage process is illustrated wherein catalyst portion 313 comprising basic component 307 of the multi-functional catalyst is introduced in a first stage into first reactor 315. Biomass may be introduced directly into the first stage reactor 315 through line 317.
  • a catalyst portion 31 1 comprising acid component 308 and metallic component 309 of the multi-functional catalyst are introduced.
  • the pyrolyzed biomass from the second stage reactor 329 is treated in solids separator 324 such that solids including spent or contaminated catalyst 330 are separated from the pyrolyzed biomass.
  • Liquids and vapors (including bio-oil) separated from the treated biomass in solids separator 324 may be further processed in order, for instance, to render boiling point equivalent fractions of renewable gasoline, renewable jet fuel, renewable diesel and/or renewable fuel oil.
  • Solids separated in solids separator 324 including spent or contaminated catalyst 330 may then be fed into catalyst regeneration unit 318 wherein at least a portion of coke deposits are burned from the spent catalyst in oxygen or an oxygen containing gas, such as air.
  • At least a portion 340 of regenerated catalyst 322 containing acid component 308, basic component 307 and metallic component 309 exiting the catalyst regeneration unit 318 may proceed via line 320 into first stage reactor 315 and/or at least another portion 342 of regenerated catalyst 322 proceeds via line 343 into second stage reactor 329.
  • regenerated catalyst 322 from catalyst regeneration unit 318 may be divided such that stream 340 contain the regenerated basic component and stream 342 comprises regenerated acidic component and regenerated metallic component.
  • a stream of fresh basic component 307 may be fed into first stage reactor 315 and a stream of fresh acidic component 308 and/or metallic component 309 may be fed into second stage reactor 329 as make-up component(s) in order to attain the desired activity of the catalyst components within each staged-reactor, as needed.
  • lower activity regenerated catalyst may optionally be removed from catalyst regeneration unit 318 in order to attain the desired activity of the catalyst within the reactor and keep solid hold- up in the unit.
  • Untreated biomass may further be admixed with regenerated basic component and be fed into first stage reactor 315 through line 317.
  • untreated biomass may be fed into line 320 where it is combined with the regenerated basic component.
  • catalyst portion 313 comprises acidic material 308 and is introduced into first stage reactor 315 and catalyst portion 311 comprises basic component 307 and metallic component 309 and is introduced into second stage reactor 329.
  • At least a portion 340 of regenerated catalyst 322 containing acid component 308, basic component 307 and metallic component 309 exiting the catalyst regeneration unit 318 may proceed via line 320 into first stage reactor 315 and/or at least another portion 342 of regenerated catalyst 322 proceeds via line 343 into second stage reactor 329.
  • regenerated catalyst 322 from catalyst regeneration unit 318 may be divided such that stream 340 comprises the regenerated acidic component and stream 342 comprises regenerated basic component and regenerated metallic component.
  • a stream of fresh acidic component 308 may be fed into first stage reactor 315 and a stream of fresh basic component 307 and/or metallic component 309 may be fed into second stage reactor 329 as make-up component(s) in order to attain the desired activity of the catalyst components within the reactor, as needed.
  • lower activity regenerated catalyst may optionally be removed from catalyst regeneration unit 318 in order to attain the desired activity of the catalyst within the reactor and keep solid hold-up in the unit.
  • catalyst portion 313 comprises metallic component 309 and is introduced into first stage reactor 315 and catalyst portion 311 comprises acidic component 308 and basic component 307 and is introduced into second stage reactor 329.
  • At least a portion 340 of regenerated catalyst 322 containing acid component 308, basic component 307 and metallic component 309 exiting the catalyst regeneration unit 318 may proceed via line 320 into first stage reactor 315 and/or at least another portion 342 of regenerated catalyst 322 proceeds via line 343 into second stage reactor 329.
  • regenerated catalyst 322 from catalyst regeneration unit 318 may be divided such that stream 340 contain regenerated the metallic component and stream 342 comprises regenerated acidic component and regenerated basic component.
  • a stream of fresh metallic component 309 may be fed into first stage reactor 315 and a stream of fresh acidic component 308 and/or fresh basic component 307 may be fed into second stage reactor 329 as make-up component(s) in order to attain the desired activity of the catalyst components within the reactor, as needed.
  • lower activity regenerated catalyst may optionally be removed from catalyst regeneration unit 318 in order to attain the desired activity of the catalyst within the reactor and keep solid hold-up in the unit.
  • FIG. 4A a two stage process system is illustrated wherein catalyst portion 413 comprising acidic component 408 and metallic component 409 of the multifunctional catalyst are introduced into first stage reactor 415.
  • Biomass 412 may be introduced directly into first stage reactor 415 through line 417.
  • catalyst portion 411 comprising basic component 407 of the multi-functional catalyst is introduced.
  • the pyrolyzed biomass from second stage reactor 429 is treated in solids separator 424 such that solids including spent or contaminated catalyst 430 are separated from the pyrolyzed biomass. Liquids and vapor (including bio-oil) separated from the treated biomass in solids separator 424 may be further processed.
  • Spent or contaminated catalyst 430 may then be fed into catalyst regeneration unit 418 wherein at least a portion of coke deposits are burned from the spent catalyst in oxygen or an oxygen containing gas, such as air.
  • the resulting regenerated catalyst 422 contains the acidic component, basic component and the metal component of the multi-functional catalyst as described herein.
  • At least a portion 440 of regenerated catalyst 422 containing acid component 408, basic component 407 and metallic component 409 exiting the catalyst regeneration unit 418 may proceed via line 420 into first stage reactor 415 and/or at least another portion 442 of regenerated catalyst 422 proceeds via line 443 into second stage reactor 429.
  • regenerated catalyst 422 from catalyst regeneration unit 418 may be divided such that stream 440 contains the regenerated acidic component and the regenerated metallic component and stream 442 comprises the regenerated basic component.
  • a stream of fresh acidic component 408 and/or fresh metallic component 409 may be fed into first stage reactor 415 and a stream of fresh basic component 407 may be fed into second stage reactor 429 as make-up component(s) in order to attain the desired activity of the catalyst components within the staged-reactor, as needed.
  • Untreated biomass may further be admixed with regenerated acidic component and regenerated metallic component and be fed into first stage reactor 415 through line 417.
  • lower activity regenerated catalyst may optionally be removed from catalyst regeneration unit 418 in order to attain the desired activity of the catalyst within the reactor and keep solid hold-up in the unit.
  • untreated biomass may be fed into line 420 where it is combined with the regenerated acidic and metallic components.
  • catalyst portion 413 comprises basic component 407 and metallic component 409 and is introduced into first stage reactor 415 and catalyst portion 41 1 comprises acidic component 408 and is introduced into second stage reactor 429.
  • At least a portion 440 of regenerated catalyst 422 containing acid component 408, basic component 407 and metallic component 409 exiting the catalyst regeneration unit 418 may proceed via line 420 into first stage reactor 415 and/or at least another portion 442 of regenerated catalyst 422 proceeds via line 443 into second stage reactor 429.
  • regenerated catalyst 422 from catalyst regeneration unit 418 may be divided such that stream 440 contain regenerated the basic component and regenerated metallic component, and stream 442 comprises regenerated acidic component.
  • a stream of fresh basic component and/or metallic component may be fed into first stage reactor 415 and a stream of acid component 409 may be fed into second stage reactor 429 as make-up component(s) in order to attain the desired activity of the catalyst components within the reactor(s).
  • lower activity regenerated catalyst may optionally be removed from catalyst regeneration unit 318 in order to attain the desired activity of the catalyst within the reactor and keep solid hold-up in the unit.
  • catalyst portion 413 comprises basic component 407 and acidic component 408 and is introduced into first stage reactor 415 and catalyst portion 411 comprises metallic component 409.
  • At least a portion 440 of regenerated catalyst 422 containing acid component 408, basic component 407 and metallic component 409 exiting the catalyst regeneration unit 418 may proceed via line 420 into first stage reactor 415 and/or at least another portion 442 of regenerated catalyst 422 proceeds via line 443 into second stage reactor 429.
  • regenerated catalyst 422 from catalyst regeneration unit 418 may be divided such that stream 440 comprises the regenerated acidic component and regenerated basic component and stream 442 comprises regenerated metallic component.
  • a stream of fresh acidic component and/or basic component may be fed into first stage reactor 415 and a stream of metallic component 409 may be fed into second stage reactor 429 as make-up component(s) in order to attain the desired activity of the catalyst components within the reactor(s).
  • lower activity regenerated catalyst may optionally be removed from catalyst regeneration unit 418 in order to attain the desired activity of the catalyst within the reactor and keep solid hold-up in the unit.
  • FIG. 5A illustrates a two stage pyrolysis system wherein catalyst component 513 comprising basic component 507 is fed into first stage reactor 515.
  • Biomass may be introduced directly into first stage reactor 515 through line 517.
  • the treated biomass may be fed into first solids separator 525 such that solids including spent or contaminated (basic) component 531 may be separated from the pyrolyzed biomass.
  • Liquids and vapor are separated from the pyrolyzed biomass and are then fed into second stage reactor 529.
  • Spent or contaminated component 531 from first solids separator 525 may then be fed into first catalyst regeneration unit 516 wherein at least a portion of coke deposits are burned from the spent component in oxygen or an oxygen containing gas, such as air.
  • the resulting regenerated (basic) component 521 may then be fed through line 540 into first stage reactor 515.
  • Untreated biomass may further be admixed with the regenerated basic component and fed into first stage reactor 515 through line 540.
  • a stream of fresh component 507 may also be fed into first stage reactor 515 and/or admixed with the regenerated basic component 521 in order to attain the desired activity of the basic catalyst component within the reactor.
  • lower activity regenerated basic component may optionally be removed from catalyst regeneration unit 516 in order to attain the desired activity of the component within the reactor and keep solid hold-up in the unit.
  • the pyrolyzed liquids and vapors (including bio-oil) substantially free of solids separated in the first solids separator 525 are introduced as vapor into second stage reactor 529 through line 542.
  • Catalyst portion 51 1 comprising acidic component 508 and metallic component 509 is fed into second stage reactor 529 through line 510.
  • the pyrolyzed biomass from second stage reactor 529 may then be fed into second solids separator 526 where solid spent or contaminated component 532 (acid component and metallic component) are separated from the liquids and vapor.
  • the liquids and vapor (including bio-oil) separated from the biomass in second solids separator 526 may be further processed to render hydrocarbon distillate for use in renewable fuels production.
  • Spent solids 532 may then be fed into second regeneration unit 519 wherein at least a portion of coke deposits are burned.
  • the regenerated catalyst component 523 from second regeneration unit 519 enriched in regenerated acidic component and regenerated metallic component may then be fed via line 542 into second stage reactor 529.
  • a stream of fresh acidic component and/or metallic component may be fed into second stage reactor 529 as needed as make-up component(s).
  • the fresh component(s) may be added directly into the reactor and/or fed into line 542 and/or admixed with the regenerated component(s).
  • lower activity regenerated acidic and/or metallic components may optionally be removed from catalyst regeneration unit 519 in order to attain the desired activity of these components within the reactor and keep solid hold-up in the unit.
  • catalyst portion 513 is comprised of acidic component 508 and catalyst portion 511 is composed of basic component 507 and metallic component 509.
  • acidic component 508 is introduced into first stage reactor 515 and basic component 507 and metallic component 509 are fed into second stage reactor 529.
  • spent component 531 comprises the spent acidic component
  • spent component 532 comprises the spent basic and metallic components.
  • regenerated component 521 comprises regenerated acidic component 508 and regenerated portion 523 comprises regenerated basic component 507 and regenerated metallic opponent 509.
  • a stream of fresh acidic component 508 may also be fed into first stage reactor 515 and/or admixed with regenerated acidic component 521 in order to attain the desired activity of the acidic catalyst component within the reactor.
  • a stream of fresh basic component 507 and/or metallic component 509 may be fed into second stage reactor 529 and/or admixed with regenerated components 523 in order to attain the desired activity of the fresh basic component and metallic component within the reactor to keep solid hold-up in the unit.
  • Lower activity regenerated acidic component may optionally be removed from first regeneration unit 516 and/or lower activity basic component 507 and/or metallic component 509 may be removed from second regeneration unit 519 in order to attain the desired activity of the catalyst component(s) in the stage 1 reactor 515 and second stage reactor 529 and keep solid(s) hold-up in the unit.
  • catalyst portion 513 is comprised of metallic component 509 and catalyst portion 511 is composed of acidic component 508 and basic component 507.
  • metallic component 509 is introduced into first stage reactor 515 and acidic component 508 and basic component 507 are fed into second stage reactor 529.
  • spent component 531 comprises the spent metallic component
  • spent component 532 comprises spent acidic and spent basic components.
  • regenerated component 521 comprises regenerated metallic component 509 and regenerated portion 523 comprises regenerated acidic component 508 and regenerated basic component 507.
  • a stream of fresh metallic component 509 may be fed into first stage reactor 515 and/or admixed with regenerated component 521 in order to attain the desired activity of the fresh metallic component within the reactor to keep solid hold-up in the unit.
  • a stream of acidic component 508 and/or basic component 507 may be fed into second stage reactor 529 and/or admixed with regenerated components 523 in order to attain the desired activity of the acidic component 508 and/or basic component 507 within the reactor to keep solid hold-up in the unit.
  • Lower activity regenerated metallic component may optionally be removed from first regeneration unit 516 and/or lower activity acidic component 508 and/or basic component 507 may be removed from second regeneration unit 519 in order to attain the desired activity of the catalyst component(s) in the stage 1 reactor 515 and second stage reactor 529 and keep solid(s) hold-up in the unit.
  • catalyst portion 613 is comprised of acidic component 608 and metallic component 609 of the multi-functional catalyst and are introduced into first stage reactor 615.
  • the basic component 607 of the multifunctional catalyst is introduced as component 611 into the second reactor 629.
  • spent component 631 comprises the spent acidic component and metallic component
  • spent component 632 comprises the spent basic component.
  • regenerated component 621 comprises regenerated acidic component 608 and regenerated metallic component 609 and regenerated portion 623 comprises regenerated acidic component 607.
  • a stream of fresh acidic component 608 and/or metallic component 609 may be fed into first stage reactor 615 and/or admixed with regenerated components 621 in order to attain the desired activity of the acidic component and/or metallic component within the reactor to keep solid hold-up in the unit.
  • a stream of basic component 607 may be fed into second stage reactor 629 and/or admixed with regenerated components 623 in order to attain the desired activity of the basic component within the reactor.
  • Lower activity regenerated acidic component and/or metallic component may optionally be removed from first regeneration unit 616 and/or lower activity basic component may be removed from second regeneration unit 619 in order to attain the desired activity of the catalyst component(s) in the stage 1 reactor 615 and second stage reactor 629 and keep solid(s) hold-up in the unit.
  • FIG. 6B a two stage process is illustrated as set forth in FIG. 6A above except catalyst portion 613 is comprised of basic component 607 and metallic component 609 and catalyst portion 611 is composed of acidic component 608.
  • the acidic component 608 of the multi-functional catalyst is introduced into second reactor 629.
  • spent component 631 comprises the spent basic component and metallic component
  • spent component 632 comprises the spent acidic component.
  • regenerated component 621 comprises regenerated basic component 607 and metallic component 609 and regenerated portion 623 comprises regenerated basic component 608.
  • a stream of fresh basic component 607 and/or metallic component 609 may be fed into first stage reactor 615 and/or admixed with regenerated components 621 in order to attain the desired activity of the basic component and/or metallic component within the reactor to keep solid hold-up in the unit.
  • a stream of acidic component 608 may be fed into second stage reactor 629 and/or admixed with regenerated component 623 in order to attain the desired activity of the acidic component within the reactor.
  • Lower activity regenerated basic component and/or metallic component may optionally be removed from first regeneration unit 616 and/or lower activity acidic component may be removed from second regeneration unit 619 in order to attain the desired activity of the catalyst component(s) in the stage 1 reactor 615 and second stage reactor 629 and keep solid(s) hold-up in the unit.
  • FIG. 6C a two stage process is illustrated as set forth in FIG. 6A above except catalyst portion 613 is comprised of basic component 607 and acidic component 608.
  • the metallic component 609 of the multi-functional catalyst is introduced in catalyst portion 61 1 into second reactor 629. It is understood then that spent component 631 comprises the spent basic component and spent acidic component and spent component 632 comprises the spent metallic component.
  • regenerated component 621 comprises regenerated basic component 607 and regenerated acidic component 608 and regenerated portion 623 comprises regenerated metallic component 609.
  • a stream of fresh acidic component 608 and/or basic component 607 may be fed into first stage reactor 615 and/or admixed with regenerated components 621 in order to attain the desired activity of the acidic component and/or basic component within the reactor to keep solid hold-up in the unit.
  • a stream of metallic component 609 may be fed into second stage reactor 629 and/or admixed with regenerated component 623 in order to attain the desired activity of the metallic component within the reactor.
  • Lower activity regenerated acidic component and/or basic component may optionally be removed from first regeneration unit 616 and/or lower activity metallic component may be removed from second regeneration unit 619 in order to attain the desired activity of the catalyst component(s) in the stage 1 reactor 615 and second stage reactor 629 and keep solid(s) hold-up in the unit.
  • a reactor system as that shown in FIG. 7 was used to assess the capabilities of the different process configurations that employ the multi-functional catalyst of the present disclosure.
  • Each stage was run at fixed bed mode.
  • Stage 1 was set at 550°C and
  • Stage 2 was set at 450°C.
  • the catalyst composition employed at each stage was adjusted to represent the ranges of the multi-functional catalyst of the present disclosure.
  • Comparative experiments were run using the same proportions of catalyst components for each experiment, which were 20% ZSM-5 + 10% USY as the acid (A) component, 30%) MgO-Al 2 0 3 as the basic (B) component and 10% Mo 2 C as the metal (M) component.
  • Three consecutive experiments were executed for each configuration and the products were online analyzed by GC/MS.
  • Catalyst 1 was composed by the B component and the M component; and Catalyst 2 was composed of the A component.
  • Catalyst 1 was composed by the B component and the M component; and Catalyst 2 was composed of the A component.
  • Catalyst 1 was composed by the B component and the M component; and Catalyst 2 was composed of the A component.
  • Catalyst 1 was composed by the B component and the M component; and Catalyst 2 was composed of the A component.
  • feed a sample of Southern Yellow Pine milled to a particle size below 1000 ⁇ was used.

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Abstract

Selon l'invention, une biomasse solide peut être convertie en hydrocarbures pouvant servir dans des applications de carburants renouvelables par introduction de la biomasse dans une unité de conversion de biomasse et par pyrolyse de la biomasse en présence d'un catalyseur multifonctionnel régénéré. Le catalyseur multifonctionnel régénéré contient un composant acide, un composant basique et un composant métallique. La biomasse est traitée dans l'unité de conversion de biomasse sur au moins deux étages, au moins un composant du catalyseur multifonctionnel régénéré étant introduit à chacun des étages.
PCT/US2015/011421 2014-01-30 2015-01-14 Procédé de conversion de biomasse en utilisant un système de catalyseur multifonctionnel Ceased WO2015116385A1 (fr)

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EP3400273A2 (fr) * 2015-10-05 2018-11-14 University Of Pretoria Catalyseur et procédé de réduction de composés oxygénés
US10392565B2 (en) 2017-12-14 2019-08-27 Savannah River Nuclear Solutions, Llc Conversion of biomass by efficient base-catalyzed decarboxylation reaction
KR102657435B1 (ko) * 2017-12-22 2024-04-17 루미리즈 홀딩 비.브이. 포름알데히드 산화를 촉진하기 위한 망가니즈 촉매 및 그의 제조 및 용도
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