WO2012058218A2 - Process for producing high quality pyrolysis oil from biomass - Google Patents

Process for producing high quality pyrolysis oil from biomass Download PDF

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Publication number
WO2012058218A2
WO2012058218A2 PCT/US2011/057697 US2011057697W WO2012058218A2 WO 2012058218 A2 WO2012058218 A2 WO 2012058218A2 US 2011057697 W US2011057697 W US 2011057697W WO 2012058218 A2 WO2012058218 A2 WO 2012058218A2
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Prior art keywords
reactor
pyrolysis
psia
torrefaction
ranging
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PCT/US2011/057697
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French (fr)
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WO2012058218A3 (en
Inventor
Daren Einar Daugaard
Kening Gong
Alexandru Platon
Samuel T. Jones
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Conocophillips Company
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Publication of WO2012058218A3 publication Critical patent/WO2012058218A3/en

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    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10CWORKING-UP PITCH, ASPHALT, BITUMEN, TAR; PYROLIGNEOUS ACID
    • C10C5/00Production of pyroligneous acid distillation of wood, dry distillation of organic waste
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/03Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by addition of hydroxy groups to unsaturated carbon-to-carbon bonds, e.g. with the aid of H2O2
    • C07C29/04Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by addition of hydroxy groups to unsaturated carbon-to-carbon bonds, e.g. with the aid of H2O2 by hydration of carbon-to-carbon double bonds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10BDESTRUCTIVE DISTILLATION OF CARBONACEOUS MATERIALS FOR PRODUCTION OF GAS, COKE, TAR, OR SIMILAR MATERIALS
    • C10B53/00Destructive distillation, specially adapted for particular solid raw materials or solid raw materials in special form
    • C10B53/02Destructive distillation, specially adapted for particular solid raw materials or solid raw materials in special form of cellulose-containing material
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10BDESTRUCTIVE DISTILLATION OF CARBONACEOUS MATERIALS FOR PRODUCTION OF GAS, COKE, TAR, OR SIMILAR MATERIALS
    • C10B57/00Other carbonising or coking processes; Features of destructive distillation processes in general
    • C10B57/02Multi-step carbonising or coking processes
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10BDESTRUCTIVE DISTILLATION OF CARBONACEOUS MATERIALS FOR PRODUCTION OF GAS, COKE, TAR, OR SIMILAR MATERIALS
    • C10B57/00Other carbonising or coking processes; Features of destructive distillation processes in general
    • C10B57/08Non-mechanical pretreatment of the charge, e.g. desulfurization
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/02Liquid carbonaceous fuels essentially based on components consisting of carbon, hydrogen, and oxygen only
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L9/00Treating solid fuels to improve their combustion
    • C10L9/08Treating solid fuels to improve their combustion by heat treatments, e.g. calcining
    • C10L9/083Torrefaction
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING 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
    • C10G2300/00Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
    • C10G2300/10Feedstock materials
    • C10G2300/1011Biomass
    • C10G2300/1014Biomass of vegetal origin
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING 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
    • C10G2300/00Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
    • C10G2300/10Feedstock materials
    • C10G2300/1011Biomass
    • C10G2300/1018Biomass of animal origin
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING 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
    • C10G2300/00Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
    • C10G2300/20Characteristics of the feedstock or the products
    • C10G2300/201Impurities
    • C10G2300/202Heteroatoms content, i.e. S, N, O, P
    • C10G2300/203Naphthenic acids, TAN
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E50/00Technologies for the production of fuel of non-fossil origin
    • Y02E50/10Biofuels, e.g. bio-diesel
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/141Feedstock
    • Y02P20/145Feedstock the feedstock being materials of biological origin
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P30/00Technologies relating to oil refining and petrochemical industry
    • Y02P30/20Technologies relating to oil refining and petrochemical industry using bio-feedstock

Definitions

  • the present invention relates generally to the conversion of biomass to fuel range hydrocarbons.
  • Biomass is any carbon containing material derived from living or formerly living organisms, such as wood, wood waste, crops, crop waste, waste, and animal waste.
  • Pyrolysis is the chemical decomposition of organic materials by heating in the absence of oxygen or other reagents. Pyrolysis can be used to convert biomass (such as lignocellulosic biomass) into pyrolysis oil or so-called bio-oil. The bio-oils obtained by pyrolysis of biomass or waste have received attention recently as an alternative source of fuel.
  • biomass produces four primary products, namely water, “bio-oil,” also known as “pyrolysis oil,” char, and various gases (H 2 , CO, C0 2 , CH 4 , and other light hydrocarbons) that do not condense, except under extreme conditions.
  • bio-oil also known as “pyrolysis oil”
  • char various gases (H 2 , CO, C0 2 , CH 4 , and other light hydrocarbons) that do not condense, except under extreme conditions.
  • gases H 2 , CO, C0 2 , CH 4 , and other light hydrocarbons
  • Fast pyrolysis is one method for the conversion of biomass to bio-oil.
  • Fast pyrolysis is the rapid thermal decomposition of organic compounds in the absence of atmospheric or added oxygen to produce liquids, char, and gas.
  • Fast pyrolysis affords operation at atmospheric pressure, moderate temperatures, and with low or no water usage.
  • Pyrolysis oil yields typically range from 50-75% mass of input biomass and are heavily feedstock dependent.
  • pyrolysis oil obtained from biomass fast pyrolysis process is chemical complex compounds comprising generally a mixture of water, light volatiles, and non-volatiles. They are in general of relatively low quality. As fuels they have a number of negative properties such as high acidity (lead to corrosion problem), substantial water content (usually in the range of 15% to 30%>), variable viscosity, low heating values (about half that of the diesel fuel), low cetane number, etc. These negative properties are related to the oxygenated compounds contained in bio-oils that result in a 45% oxygen content. In general, the pyrolysis oil has total acidity number (TAN) value of approximately 100. The desired TAN value for transportation fuel is less than 10.
  • TAN total acidity number
  • this invention discloses a process for producing high quality pyrolysis oil from biomass by utilizing a torrefaction pretreatment step for biomass pyrolysis process wherein the pretreatment step improves the quality of the pyrolysis oil by reducing acidity.
  • the disclosed process comprises at least the following steps: a) a step of subjecting a biomass feedstock to a thermal treatment in a reactor A under a torrefaction reaction condition to produce an torrefied biomass feedstock; and b) a step of pyrolyzing the torrefied biomass feedstock in a reactor B under a pyrolysis reaction condition to form a pyrolysis oil product.
  • the torrefaction reaction condition includes a temperature ranging from 180°C to 350°C, a pressure ranging from atmospheric pressure to 500 psia, (but optionally, ranging as low as 0.1 psia) and a residence time ranging from 1 minute to 24 hours.
  • the pyrolysis reaction condition includes a temperature ranging from 375°C to 700°C, a pressure ranging from vacuum conditions (0.1 psia) to 1000 psia., and a residence time ranging from 0.1 to 200 seconds.
  • the pyrolysis oil product according to the current invention has a TAN number between 80 and 200.
  • Embodiments of the invention relate to a process to utilize a torrefaction pretreatment step for biomass pyrolysis process.
  • This pretreatment improves the quality of the pyrolysis oil by reducing acidity.
  • the inventive process shows that as a pretreatment to pyrolysis, resulting pyrolysis oil obtained from torrefied biomass has approximately 25% lower acetic acid than that from untorrefied biomass pyrolysis oil.
  • biomass includes any renewable source (living or formerly living), but does not include oil, natural gas, and/or petroleum. Biomass thus includes but is not limited to wood, paper, crops, animal and plant fats, biological waste, algae, and the like.
  • a step of subjecting a biomass feedstock to a thermal treatment in a reactor under a torrefaction reaction condition to produce a torrefied biomass feedstock there is disclosed a step of subjecting a biomass feedstock to a thermal treatment in a reactor under a torrefaction reaction condition to produce a torrefied biomass feedstock.
  • Torrefaction consists of a slow heating of biomass feedstock in an inert atmosphere to produce a solid with lower hemicellulose content, higher energy density, nearly moisture free ( ⁇ 3 wt%), and low resistance to fracture (brittle).
  • Any standard torrefaction reactor can be used to torrefy the biomass feedstock.
  • Exemplary reactor configurations include without limitations augers reactor, ablative reactor, rotating cones reactor, fluidized-bed reactor, entrained-flow reactor, vacuum moving-bed reactor, transported-bed reactor, and fixed-bed reactor.
  • any standard torrefaction reaction condition can be used to torrefy the biomass feedstock in the torrefaction reactor.
  • a person skilled in the art can readily select a combination of temperature, pressure, and residence time that produces a torrefied product.
  • the torrefaction reaction conditions include a temperature ranging from 180°C to 350°C, a pressure ranging from atmospheric pressure to 500 psia, and a residence time ranging from 1 minute to 24 hours.
  • the torrefaction reaction conditions include a temperature ranging from 220°C to 280°C, a pressure ranging from 11 psia to 30 psia, and a residence time ranging from 5 to 20 minutes.
  • the torrefaction reaction conditions include a temperature ranging from 180°C to 350°C, a pressure ranging from 0.1 psia to 500 psia, and a residence time ranging from 1 minute to 24 hours.
  • torrefaction is carried out in the presence of a catalyst material selected from a group consisting solid acid catalyst such as ZSM5, solid base catalyst such as Hydrotalcite, silica catalyst such as Diatomite, silica-alumina catalyst such as Kaolin, Group B metal oxide catalyst such as Ammonium Molybdate, pyrolytic char and any combination thereof.
  • a catalyst material selected from a group consisting solid acid catalyst such as ZSM5, solid base catalyst such as Hydrotalcite, silica catalyst such as Diatomite, silica-alumina catalyst such as Kaolin, Group B metal oxide catalyst such as Ammonium Molybdate, pyrolytic char and any combination thereof.
  • the torrefaction reaction is carried out in the absence of diatomic oxygen in an inert gas atmosphere such as nitrogen, argon, steam, carbon oxides, etc.
  • the torrefaction reaction is carried out in a reducing gas atmosphere that comprises carbon monoxide.
  • torrefaction may be carried out with other reactants such as hydrogen
  • the torrefied biomass according to various embodiments of the invention may be added to a pyrolysis reactor for further processing.
  • the torrefied biomass is pyrolyzed in a pyrolysis reactor under pyrolysis reaction conditions to form a pyrolysis oil product.
  • Pyrolysis which is the thermal decomposition of a substance into its elemental components and/or smaller molecules, is used in various methods developed for producing hydrocarbons, including but not limited to hydrocarbon fuels, from biomass. Pyrolysis requires moderate temperatures, generally greater than about 325°C, such that the feed material is sufficiently decomposed to produce products which may be used as hydrocarbon building blocks.
  • Embodiments of the inventive process use any standard pyrolysis reactor providing sufficient heat to pyrolyze torrefied biomass feedstock, including without limitation, auger reactor, ablative reactor, a bubbling fluidized bed reactor, circulating fluidized beds/transport reactor, rotating cone pyrolyzer, vacuum pyrolyzer, and the like.
  • any standard pyrolysis reaction condition can be used to pyrolyze the torrefied biomass feedstock in a pyrolysis reactor.
  • a person skilled in the art can readily select a combination of temperature, pressure, and residence time that produces a pyrolyzed product.
  • the pyrolysis reaction condition includes a temperature ranging from 375°C to 700°C, a pressure ranging from vacuum conditions of 0.1 psia up to 1000 psia., and a residence time ranging from 0.1 to 200 seconds.
  • the pyrolysis reaction condition includes a temperature ranging from 425°C to 525°C, a pressure ranging from atmospheric pressure to 300 psia., and a residence time ranging from 0.5 to 2 seconds.
  • a variety of catalysts may be used for the pyrolysis reaction.
  • the pyrolysis reaction is carried out in the presence of a catalyst material selected from a group consisting of solid acid catalyst such as ZSM5, solid base catalyst such as Hydrotalcite, silica catalyst such as Diatomite, silica-alumina catalyst such as Kaolin, Group B metal oxide catalyst such as Ammonium Molybdate, pyrolytic char and any combination thereof.
  • a catalyst material selected from a group consisting of solid acid catalyst such as ZSM5, solid base catalyst such as Hydrotalcite, silica catalyst such as Diatomite, silica-alumina catalyst such as Kaolin, Group B metal oxide catalyst such as Ammonium Molybdate, pyrolytic char and any combination thereof.
  • the pyrolysis oil product obtained according to some embodiments of the present invention has a TAN number between 80 and 200.
  • the pyrolysis oil product obtained according to some other embodiments of the present invention has a TAN number between less than 20 and 50.
  • the pyrolysis oil obtained from biomass fast pyrolysis process is of relatively low quality.
  • pyrolysis oil has TAN value of approximately 100.
  • the desired TAN value for transportation fuel is less than 10.
  • the step of pretreatment of torrefaction can be easily integrated with the pyrolysis step.
  • the pretreatment step improves the quality of the feed quality of pyrolysis step and therefore results in higher quality of pyrolysis oil product including low TAN value.
  • such integrated process reduces the operating cost and capital investment of post treatment process.

Abstract

This invention relates to a process to utilize a torrefaction pretreatment step for biomass pyrolysis process. This pretreatment improves the quality of the pyrolysis oil by reducing acidity. The inventive process shows that as a pretreatment to pyrolysis, resulting pyrolysis oil obtained from torrefied biomass has approximately 25% lower acetic acid than that from untorrefied biomass pyrolysis oil.

Description

PROCESS FOR PRODUCING HIGH QUALITY
PYROLYSIS OIL FROM BIOMASS
CROSS-REFERENCE TO RELATED APPLICATIONS
[0001] None.
STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH OR
DEVELOPMENT
[0002] None.
FIELD OF THE INVENTION
[0003] The present invention relates generally to the conversion of biomass to fuel range hydrocarbons.
BACKGROUND OF THE INVENTION
[0004] Due to governmental legislation as mandated in the Renewable Fuels Standards (RFS), the use of renewable energy sources is becoming increasingly necessary to reduce emissions of carbon based fuels and provide alternatives to petroleum based energy and feedstock. One of the alternatives being explored is the use of biomass. Biomass is any carbon containing material derived from living or formerly living organisms, such as wood, wood waste, crops, crop waste, waste, and animal waste.
[0005] Pyrolysis is the chemical decomposition of organic materials by heating in the absence of oxygen or other reagents. Pyrolysis can be used to convert biomass (such as lignocellulosic biomass) into pyrolysis oil or so-called bio-oil. The bio-oils obtained by pyrolysis of biomass or waste have received attention recently as an alternative source of fuel.
[0006] Generally the pyrolysis of biomass produces four primary products, namely water, "bio-oil," also known as "pyrolysis oil," char, and various gases (H2, CO, C02, CH4, and other light hydrocarbons) that do not condense, except under extreme conditions. For exemplary purposes, the pyrolysis decomposition products of wood from white spruce and poplar trees are shown in Table 1.
Table 1
Figure imgf000003_0001
[0007] Fast pyrolysis is one method for the conversion of biomass to bio-oil. Fast pyrolysis is the rapid thermal decomposition of organic compounds in the absence of atmospheric or added oxygen to produce liquids, char, and gas. Fast pyrolysis affords operation at atmospheric pressure, moderate temperatures, and with low or no water usage. Pyrolysis oil yields typically range from 50-75% mass of input biomass and are heavily feedstock dependent.
[0008] The major advantage of these fuels is that these are C02 neutral and contain a very low fraction of bonded sulfur and nitrogen. Thus, they contribute very little to the emission of greenhouse gases or other regulated air pollutants.
[0009] There has been a considerable effort in the past to develop pyrolysis processes for the conversion of biomass and waste to liquids for the express purpose of producing renewable liquid fuels suitable for use in boilers, gas turbines and diesel engines.
[0010] However, pyrolysis oil obtained from biomass fast pyrolysis process is chemical complex compounds comprising generally a mixture of water, light volatiles, and non-volatiles. They are in general of relatively low quality. As fuels they have a number of negative properties such as high acidity (lead to corrosion problem), substantial water content (usually in the range of 15% to 30%>), variable viscosity, low heating values (about half that of the diesel fuel), low cetane number, etc. These negative properties are related to the oxygenated compounds contained in bio-oils that result in a 45% oxygen content. In general, the pyrolysis oil has total acidity number (TAN) value of approximately 100. The desired TAN value for transportation fuel is less than 10.
[0011] There has been a considerable effort in the past to address the high TAN problem by post treatment or upgrading the pyrolysis oils before they are used as a regular fuel. Most method essentially involves the removal of oxygen. Particular attention has been focused on hydrotreating using conventional petroleum catalysts, for example, cobalt-molybdenum or nickel-molybdenum on alumina to produce essentially oxygen- free naphthas. Since pyrolysis liquids typically contain between 30 to 50 wt % of oxygen, complete removal of oxygen requires a substantial consumption of hydrogen which represents a major and prohibitive cost.
[0012] Therefore, developing a new method or process for improving quality of pyrolysis oil would be a significant contribution to the art. BRIEF SUMMARY OF THE DISCLOSURE
[0013] Generally speaking, this invention discloses a process for producing high quality pyrolysis oil from biomass by utilizing a torrefaction pretreatment step for biomass pyrolysis process wherein the pretreatment step improves the quality of the pyrolysis oil by reducing acidity.
[0014] The disclosed process comprises at least the following steps: a) a step of subjecting a biomass feedstock to a thermal treatment in a reactor A under a torrefaction reaction condition to produce an torrefied biomass feedstock; and b) a step of pyrolyzing the torrefied biomass feedstock in a reactor B under a pyrolysis reaction condition to form a pyrolysis oil product.
[0015] The torrefaction reaction condition includes a temperature ranging from 180°C to 350°C, a pressure ranging from atmospheric pressure to 500 psia, (but optionally, ranging as low as 0.1 psia) and a residence time ranging from 1 minute to 24 hours. The pyrolysis reaction condition includes a temperature ranging from 375°C to 700°C, a pressure ranging from vacuum conditions (0.1 psia) to 1000 psia., and a residence time ranging from 0.1 to 200 seconds. The pyrolysis oil product according to the current invention has a TAN number between 80 and 200.
BRIEF DESCRIPTION OF THE DRAWINGS
[0016] None.
DETAILED DESCRIPTION
[0017] Embodiments of the invention relate to a process to utilize a torrefaction pretreatment step for biomass pyrolysis process. This pretreatment improves the quality of the pyrolysis oil by reducing acidity. The inventive process shows that as a pretreatment to pyrolysis, resulting pyrolysis oil obtained from torrefied biomass has approximately 25% lower acetic acid than that from untorrefied biomass pyrolysis oil. [0018] As used herein, the term "biomass" includes any renewable source (living or formerly living), but does not include oil, natural gas, and/or petroleum. Biomass thus includes but is not limited to wood, paper, crops, animal and plant fats, biological waste, algae, and the like.
[0019] According to one embodiment of the invention, there is disclosed a step of subjecting a biomass feedstock to a thermal treatment in a reactor under a torrefaction reaction condition to produce a torrefied biomass feedstock.
[0020] Torrefaction consists of a slow heating of biomass feedstock in an inert atmosphere to produce a solid with lower hemicellulose content, higher energy density, nearly moisture free (< 3 wt%), and low resistance to fracture (brittle).
[0021] Any standard torrefaction reactor can be used to torrefy the biomass feedstock. Exemplary reactor configurations include without limitations augers reactor, ablative reactor, rotating cones reactor, fluidized-bed reactor, entrained-flow reactor, vacuum moving-bed reactor, transported-bed reactor, and fixed-bed reactor.
[0022] Any standard torrefaction reaction condition can be used to torrefy the biomass feedstock in the torrefaction reactor. A person skilled in the art can readily select a combination of temperature, pressure, and residence time that produces a torrefied product. In one embodiment, the torrefaction reaction conditions include a temperature ranging from 180°C to 350°C, a pressure ranging from atmospheric pressure to 500 psia, and a residence time ranging from 1 minute to 24 hours. In another embodiment, the torrefaction reaction conditions include a temperature ranging from 220°C to 280°C, a pressure ranging from 11 psia to 30 psia, and a residence time ranging from 5 to 20 minutes. In yet another alternative embodiment, the torrefaction reaction conditions include a temperature ranging from 180°C to 350°C, a pressure ranging from 0.1 psia to 500 psia, and a residence time ranging from 1 minute to 24 hours.
[0023] A variety of catalysts may be used for torrefaction reaction. In some embodiments, torrefaction is carried out in the presence of a catalyst material selected from a group consisting solid acid catalyst such as ZSM5, solid base catalyst such as Hydrotalcite, silica catalyst such as Diatomite, silica-alumina catalyst such as Kaolin, Group B metal oxide catalyst such as Ammonium Molybdate, pyrolytic char and any combination thereof. [0024] In some embodiments, the torrefaction reaction is carried out in the absence of diatomic oxygen in an inert gas atmosphere such as nitrogen, argon, steam, carbon oxides, etc. In some embodiments, the torrefaction reaction is carried out in a reducing gas atmosphere that comprises carbon monoxide. Also, torrefaction may be carried out with other reactants such as hydrogen, ammonia, etc.
[0025] The torrefied biomass according to various embodiments of the invention may be added to a pyrolysis reactor for further processing. In some embodiments, the torrefied biomass is pyrolyzed in a pyrolysis reactor under pyrolysis reaction conditions to form a pyrolysis oil product.
[0026] Pyrolysis, which is the thermal decomposition of a substance into its elemental components and/or smaller molecules, is used in various methods developed for producing hydrocarbons, including but not limited to hydrocarbon fuels, from biomass. Pyrolysis requires moderate temperatures, generally greater than about 325°C, such that the feed material is sufficiently decomposed to produce products which may be used as hydrocarbon building blocks.
[0027] Embodiments of the inventive process use any standard pyrolysis reactor providing sufficient heat to pyrolyze torrefied biomass feedstock, including without limitation, auger reactor, ablative reactor, a bubbling fluidized bed reactor, circulating fluidized beds/transport reactor, rotating cone pyrolyzer, vacuum pyrolyzer, and the like.
[0028] Any standard pyrolysis reaction condition can be used to pyrolyze the torrefied biomass feedstock in a pyrolysis reactor. A person skilled in the art can readily select a combination of temperature, pressure, and residence time that produces a pyrolyzed product. In one embodiment, the pyrolysis reaction condition includes a temperature ranging from 375°C to 700°C, a pressure ranging from vacuum conditions of 0.1 psia up to 1000 psia., and a residence time ranging from 0.1 to 200 seconds. In another embodiment, the pyrolysis reaction condition includes a temperature ranging from 425°C to 525°C, a pressure ranging from atmospheric pressure to 300 psia., and a residence time ranging from 0.5 to 2 seconds.
[0029] A variety of catalysts may be used for the pyrolysis reaction. In one embodiment, the pyrolysis reaction is carried out in the presence of a catalyst material selected from a group consisting of solid acid catalyst such as ZSM5, solid base catalyst such as Hydrotalcite, silica catalyst such as Diatomite, silica-alumina catalyst such as Kaolin, Group B metal oxide catalyst such as Ammonium Molybdate, pyrolytic char and any combination thereof.
[0030] The pyrolysis oil product obtained according to some embodiments of the present invention has a TAN number between 80 and 200. The pyrolysis oil product obtained according to some other embodiments of the present invention has a TAN number between less than 20 and 50.
[0031] The following examples of certain embodiments of the invention are given. Each example is provided by way of explanation of the invention, one of many embodiments of the invention, and the following examples should not be read to limit, or define, the scope of the invention.
Example 1 :
[0032] The comparison study of the process of torrefaction prior to pyrolysis has been performed in a micropyrolysis unit. The reactions were carried out at torrefaction temperatures ranging from 179°C to 321°C and pyrolysis temperatures ranging from 379°C to 521°C with no catalyst loading. In addition, a wide variety of biomass was tested including red oak, switchgrass, miscanthus, and corn stover pellets. Comparative pyrolysis tests were run without the torrefaction pretreatment at the same pyrolysis temperatures.
Results:
[0033] The experimental results indicating the reduction of acetic acid in the pyrolysis product due to torrefaction are shown as follows:
Table I. Average Acetic Acid Yield.
Figure imgf000008_0001
1. Mass of acetic acid over mass of biomass
2. Acetic acid peak area over total peak area by GC/MS
3. Torrefaction - pyrolysis acetic acid level relative to pyrolysis acetic acid level [0034] The result above shows that the acetic acid concentration in pyrolysis oil products was reduced by 18 to 39% with this pretreatment than that from un-torrefied biomass. The resulting pyrolysis oil would have a similar reduction in TAN (total acid number) value as -80% of the TAN is due to acetic acid in pyrolysis oils.
Discussion:
[0035] As discussed above, the pyrolysis oil obtained from biomass fast pyrolysis process is of relatively low quality. In general, pyrolysis oil has TAN value of approximately 100. The desired TAN value for transportation fuel is less than 10.
[0036] The results above shows that using torrefied biomass as a pretreated feed for pyrolysis helps reduce TAN (total acid number) of the pyrolysis oil product. The pretreatment by torrefaction according to the current invention helps to significantly reduce the TAN value of the pyrolysis oil product by 25%. This is mainly attributed to the release of acetic acid in the torrefaction step.
[0037] The step of pretreatment of torrefaction can be easily integrated with the pyrolysis step. The pretreatment step improves the quality of the feed quality of pyrolysis step and therefore results in higher quality of pyrolysis oil product including low TAN value. In addition, such integrated process reduces the operating cost and capital investment of post treatment process.
[0038] It should be noted that, as used in this specification and the appended claims, the singular forms "a," "an," and "the" include plural references unless the content clearly dictates otherwise. Thus, for example, reference to a composition containing "a compound" includes a mixture of two or more compounds. It should also be noted that the term "or" is generally employed in its sense including "and/or" unless the content clearly dictates otherwise. It should also be noted that, as used in this specification and the appended claims, the phrase "configured" describes a system, apparatus, or other structure that is constructed or configured to perform a particular task or adopt a particular configuration. The phrase "configured" can be used interchangeably with other similar phrases such as arranged and configured, constructed and arranged, constructed, manufactured and arranged, and the like.
[0039] Although the systems and processes described herein have been described in detail, it should be understood that various changes, substitutions, and alterations can be made without departing from the spirit and scope of the invention as defined by the following claims. Those skilled in the art may be able to study the preferred
embodiments and identify other ways to practice the invention that are not exactly as described herein. It is the intent of the inventors that variations and equivalents of the invention are within the scope of the claims, while the description, abstract and drawings are not to be used to limit the scope of the invention. The invention is specifically intended to be as broad as the claims below and their equivalents. In closing, it should be noted that each and every claim below is hereby incorporated into this detailed description or specification as an additional embodiments of the present invention.

Claims

THAT WHICH IS CLAIMED:
1. A process for producing pyrolysis oil product from biomass comprising at least the following steps:
a) a step of subjecting a biomass feedstock to a thermal treatment in a reactor A under a torrefaction reaction condition to produce an torrefied biomass feedstock;
b) a step of pyrolyzing said torrefied biomass feedstock in a reactor B under a pyrolysis reaction condition to form a pyrolysis oil product,
wherein said torrefaction reaction conditions includes a temperature ranging from 180°C to 350°C, a pressure ranging from 11 psia to 500 psia, and a residence time ranging from 1 minute to 24 hours,
wherein said pyrolysis reaction conditions includes a temperature ranging from 375°C to 700°C, a pressure ranging from 0.1 psia to 1000 psia, and a residence time ranging from 0.1 to 200 second, and
wherein said pyrolysis oil product has a TAN number between 80 and 200.
2. The process of claim 1,
wherein said torrefaction reaction conditions includes a temperature ranging from 220°C to 280°C, a pressure ranging from 11 psia to 30 psia, and a residence time ranging from 5 to 20 minutes,
wherein said pyrolysis reaction conditions includes a temperature ranging from 425°C to 525°C, a pressure ranging from atmospheric pressure to 300 psia., and a residence time ranging from 0.5 to 2 seconds, and
wherein said pyrolysis oil product has a TAN number between 20 and 50.
3. The process of claim 1 or 2, wherein said torrefaction reaction is carried out in said reactor A selected from a group consisting of an augers reactor, an ablative reactor, a rotating cones reactor, a fluidized-bed reactor, an entrained-flow reactor, a vacuum moving-bed reactor, a transported-bed reactor, and a fixed-bed reactor.
4. The process of any preceding claim, wherein said pyrolysis reaction is carried out in said reactor B selected from a group consisting of an auger reactor, an ablative reactor, a bubbling fluidized bed reactor, a circulating fluidized bed/transport reactor, a rotating cone pyrolyzer, and a vacuum pyrolyzer.
5. The process of any preceding claim, wherein said torrefaction reaction is carried out in the presence of a catalytic material selected from a group consisting acid catalysts, solid base catalysts, silica catalysts, silica-alumina catalysts, Group B metal oxide catalysts, pyrolytic char and any combination thereof.
6. The process of any of claims 1-4, wherein said torrefaction reaction is carried out in the presence of a catalytic material selected from a group consisting ZSM5, Hydrotalcite, Diatomite, Kaolin, Ammonium Molybdate, pyrolytic char and any combination thereof.
7. The process of any preceding claim, wherein said pyrolysis reaction is carried out in the presence of a catalytic material selected from a group consisting acid catalyst, solid base catalyst, silica catalyst, silica-alumina catalyst, Group B metal oxide catalyst, pyrolytic char and any combination thereof.
8. The process of any of claims 1-6, wherein said pyrolysis reaction is carried out in the presence of a catalytic material selected from a group consisting ZSM5, Hydrotalcite, Diatomite, Kaolin, Ammonium Molybdate, pyrolytic char and any combination thereof.
9. The process of any preceding claim, wherein said torrefaction reaction is carried out in the absence of diatomic oxygen in an inert gas atmosphere comprising nitrogen, argon, steam or carbon oxide.
10. The process of any preceding claim, wherein said torrefaction reaction is carried out in a reducing gas atmosphere.
11. The process of any preceding claim, wherein said torrefaction reaction is carried out with a reactant comprising hydrogen or ammonia.
12. The process of any preceding claim, wherein said biomass feedstock is selected from the group consisting of, wood, paper, crops, animal and plant fats, biological waste, algae and mixture thereof.
13. The process of any proceeding claim, wherein said torrefaction reaction
conditions includes a temperature ranging from 180°C to 350°C, a pressure ranging from 0.1 psia to 500 psia, and a residence time ranging from 1 min to 24 hours.
14. A pyro lysis oil produced by a method according to any preceding claim.
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Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104263390A (en) * 2014-09-22 2015-01-07 中国水产科学研究院南海水产研究所 Poly-generation utilization method based on collaborative microwave pyrolysis of seaweeds and aquatic invasive plants
CN104479766A (en) * 2014-12-17 2015-04-01 河南理工大学 Novel method for preparing algae environment-friendly diesel by virtue of one-pot process
WO2015196841A1 (en) * 2014-06-24 2015-12-30 华南农业大学 Continuous pyrolysis and carbonization method of agricultural and forestry biomass
WO2016190759A1 (en) * 2015-05-25 2016-12-01 23 Rs Coras Sp Z O.O. A method for catalytic processing of waste fat into liquid fuels
WO2017099495A1 (en) * 2015-12-08 2017-06-15 연세대학교 원주산학협력단 Method for producing bio-oil using torrefaction and fast pyrolysis process
KR20180079148A (en) * 2016-12-30 2018-07-10 대한민국(산림청 국립산림과학원장) Torrefaction unification reactor for manufacturing bio-oil

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8669405B2 (en) * 2011-02-11 2014-03-11 Kior, Inc. Stable bio-oil
US9206365B2 (en) * 2012-01-10 2015-12-08 Kior, Llc Fungible bio-oil
US9670413B2 (en) 2012-06-28 2017-06-06 Ensyn Renewables, Inc. Methods and apparatuses for thermally converting biomass
US9175235B2 (en) 2012-11-15 2015-11-03 University Of Georgia Research Foundation, Inc. Torrefaction reduction of coke formation on catalysts used in esterification and cracking of biofuels from pyrolysed lignocellulosic feedstocks
CN106398726B (en) * 2016-10-31 2019-05-28 新奥生态环境治理有限公司 A kind of composting charing method
CN106635075B (en) * 2016-11-22 2019-10-01 新奥生态环境治理有限公司 A kind of production method of bio-fuel
CN106554789B (en) * 2016-11-22 2020-01-07 新奥生态环境治理有限公司 Comprehensive garbage treatment method
KR101856475B1 (en) 2016-12-30 2018-05-10 대한민국 Asymmetric reactor for manufacturing bio-oil
CN115181583A (en) * 2022-07-07 2022-10-14 浙江大学 Method and system for preparing liquid fuel by biomass catalytic pyrolysis coupled online quality improvement

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4497637A (en) * 1982-11-22 1985-02-05 Georgia Tech Research Institute Thermochemical conversion of biomass to syngas via an entrained pyrolysis/gasification process
FR2904405B1 (en) * 2006-07-31 2008-10-31 Inst Francais Du Petrole PROCESS FOR PREPARING A BIOMASS-CONTAINING LOAD FOR SUBSEQUENT GASIFICATION
FR2910488B1 (en) * 2006-12-20 2010-06-04 Inst Francais Du Petrole BIOMASS CONVERSION PROCESS FOR THE PRODUCTION OF SYNTHESIS GAS.
US20090077892A1 (en) * 2007-07-27 2009-03-26 Shulenberger Arthur M Biomass energy conversion apparatus and method
EP2105486A1 (en) * 2008-03-25 2009-09-30 KiOR Inc. Low total acid number bio-crude
US8552233B2 (en) * 2008-12-16 2013-10-08 Kior Inc. Pretreatment of biomass with carbonaceous material
WO2010102145A1 (en) * 2009-03-04 2010-09-10 Washington State University Systems and processes for producing bio-fuels from lignocellulosic materials
US8217212B2 (en) * 2009-04-01 2012-07-10 Paoluccio John A Sequencing retort liquid phase torrefication processing apparatus and method
US20120017494A1 (en) * 2010-07-26 2012-01-26 Uop Llc Processes for producing low acid biomass-derived pyrolysis oils
US8100990B2 (en) * 2011-05-15 2012-01-24 Avello Bioenery, Inc. Methods for integrated fast pyrolysis processing of biomass

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
None

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2015196841A1 (en) * 2014-06-24 2015-12-30 华南农业大学 Continuous pyrolysis and carbonization method of agricultural and forestry biomass
US10253263B2 (en) 2014-06-24 2019-04-09 South China Agricultural University Method of continuous pyrolysis and carbonization of agricultural and forestry biomass
CN104263390A (en) * 2014-09-22 2015-01-07 中国水产科学研究院南海水产研究所 Poly-generation utilization method based on collaborative microwave pyrolysis of seaweeds and aquatic invasive plants
CN104479766A (en) * 2014-12-17 2015-04-01 河南理工大学 Novel method for preparing algae environment-friendly diesel by virtue of one-pot process
WO2016190759A1 (en) * 2015-05-25 2016-12-01 23 Rs Coras Sp Z O.O. A method for catalytic processing of waste fat into liquid fuels
WO2017099495A1 (en) * 2015-12-08 2017-06-15 연세대학교 원주산학협력단 Method for producing bio-oil using torrefaction and fast pyrolysis process
KR101772165B1 (en) * 2015-12-08 2017-08-28 연세대학교 원주산학협력단 Method for manufacturing biocrude-oil by torrefaction and fast pyrolysis
KR20180079148A (en) * 2016-12-30 2018-07-10 대한민국(산림청 국립산림과학원장) Torrefaction unification reactor for manufacturing bio-oil
KR101887028B1 (en) * 2016-12-30 2018-08-10 대한민국 Torrefaction unification reactor for manufacturing bio-oil

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