CN103189479B - 可再生生物馏分油的生产 - Google Patents

可再生生物馏分油的生产 Download PDF

Info

Publication number
CN103189479B
CN103189479B CN201180052116.4A CN201180052116A CN103189479B CN 103189479 B CN103189479 B CN 103189479B CN 201180052116 A CN201180052116 A CN 201180052116A CN 103189479 B CN103189479 B CN 103189479B
Authority
CN
China
Prior art keywords
distillate
biological
renewable
oil
composition
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
CN201180052116.4A
Other languages
English (en)
Other versions
CN103189479A (zh
Inventor
M·M·拉米尔兹科雷朵斯
J·索里尔斯
张长安
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Inaeris Technologies LLC
Original Assignee
Kior Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Kior Inc filed Critical Kior Inc
Publication of CN103189479A publication Critical patent/CN103189479A/zh
Application granted granted Critical
Publication of CN103189479B publication Critical patent/CN103189479B/zh
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • 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
    • 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
    • C10G1/00Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal
    • C10G1/02Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal by distillation
    • 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
    • C10G1/00Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal
    • C10G1/08Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal with moving catalysts
    • 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
    • C10G3/00Production of liquid hydrocarbon mixtures from oxygen-containing organic materials, e.g. fatty oils, fatty acids
    • C10G3/42Catalytic treatment
    • 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
    • C10L1/04Liquid carbonaceous fuels essentially based on blends of hydrocarbons
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11BPRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
    • C11B13/00Recovery of fats, fatty oils or fatty acids from waste materials
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11CFATTY ACIDS FROM FATS, OILS OR WAXES; CANDLES; FATS, OILS OR FATTY ACIDS BY CHEMICAL MODIFICATION OF FATS, OILS, OR FATTY ACIDS OBTAINED THEREFROM
    • C11C3/00Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom
    • 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
    • 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
    • C10G2300/1037Hydrocarbon fractions
    • 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
    • C10G2300/30Physical properties of feedstocks or products
    • C10G2300/301Boiling range
    • 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
    • C10G2300/80Additives
    • 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
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E50/00Technologies for the production of fuel of non-fossil origin
    • Y02E50/30Fuel from waste, e.g. synthetic alcohol or 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
    • Y02P30/00Technologies relating to oil refining and petrochemical industry
    • Y02P30/20Technologies relating to oil refining and petrochemical industry using bio-feedstock
    • 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
    • Y02WCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
    • Y02W30/00Technologies for solid waste management
    • Y02W30/50Reuse, recycling or recovery technologies
    • Y02W30/74Recovery of fats, fatty oils, fatty acids or other fatty substances, e.g. lanolin or waxes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
  • Liquid Carbonaceous Fuels (AREA)

Abstract

提供了一种方法和***,用于从生物油中分离轻质馏分、生物馏分油馏分(组合物)和重质馏分,和用于生产包含至少部分生物馏分油组合物和稳定添加剂的可再生馏分油。该方法包括基于各自的沸点将生物油分离为轻质、生物馏分油和重质馏分。将至少一部分生物馏分油组合物和稳定剂与石油衍生柴油范围的物流不进行任何预先加氢处理共混,由此提供可再生馏分油组合物。

Description

可再生生物馏分油的生产
技术领域
本发明总体上涉及从生物油中分离生物馏分油组合物的方法和***。更具体地,本发明涉及包含至少部分生物馏分油组合物的可再生馏分油的生产。
背景技术
由于化石燃料不断升高的成本和环境忧虑,可再生能源变得日益重要。可再生燃料源的开发提供了减少对化石燃料依赖的途径。因此,许多不同领域的可再生燃料研究正在探索和发展。
由于成本低和可获得性广泛,生物质作为可再生燃料研究中理想的原料正受到越来越多的重视。所以,开发出许多使用生物质作为原料生产有用的生物燃料和/或专用化学品的不同的转化方法。现有的生物质转化方法包括例如燃烧、气化、慢速热解、快速热解、液化和酶转化。可从上述生物质转化方法获得的有用产品之一是通常称为“生物油”的液体产品。生物油可被处理成运输燃料、烃化学品和/或专用化学品。
尽管生物质转化方法近来取得了进展,但是许多现有的生物质转化方法生产的是氧含量高的低质生物油,这样的生物油难以(如果不是不可能的话)分离为多种馏分。由于生物油中的氧含量高,这些生物油需要大规模的二次提质以用作运输燃料和/或用作燃料添加剂。另外,这些得自生物油的运输燃料和/或燃料添加剂质量随生物油中原始氧含量而不同。
因此,需要改进的方法和***,用来将生物油分离为多种馏分如生物馏分油,和将该馏分用作可再生燃料的共混组分。
发明内容
在一个实施方案中,本发明涉及一种生产生物馏分油组合物的方法,该方法包括:(a)在包含催化剂的转化反应器中转化生物质,由此生成包含蒸气转化产物的转化反应器流出物;(b)将至少一部分蒸气转化产物冷凝,由此提供总氧含量小于约15wt%的生物油;和(c)从生物油中分离生物馏分油组合物,其中至少约75wt%的生物馏分油组合物的沸点为约180-380℃,和其中生物馏分油组合物包含至少约50或40wt%的无氧烃。
在另一个实施方案中,本发明涉及一种生产可再生馏分油的方法,该方法包括:(a)将生物油分离为至少生物馏分油组合物,其中至少约75wt%的生物馏分油组合物的沸点为约180-380℃,其中生物油未预先经过脱氧加氢处理步骤;和(b)将至少一部分生物馏分油组合物与石油衍生馏分油范围的物流和具有表面活性剂性能的稳定添加剂合并,由此生成具有单一澄清相的可再生馏分油,其中可再生馏分油包含含量为约5-99wt%的石油衍生馏分油范围的物流、含量为至少约0.5wt%的生物馏分油组合物和含量为约0.5-25wt%的稳定添加剂。
在另一个实施方案中,本发明涉及一种总氧含量小于约15wt%的生物馏分油组合物,其中至少约75wt%的生物馏分油组合物的沸点为约180-380℃,和生物馏分油组合物包含至少约50或40wt%的无氧烃。
在另一个实施方案中,本发明涉及一种可再生馏分油组合物,该组合物包含含量为约5-99wt%的石油衍生馏分油范围的物流、含量为至少约0.5wt%的生物馏分油组合物和含量为约0.5-25wt%的具有表面活性剂性能的稳定添加剂。
附图说明
图1是本发明一个实施方案的生物质转化***的示意图。
具体实施方式
图1描述了生物质转化***10,它包括用于将生物油分离为多种馏分或燃料添加剂以及将生物馏分油组合物与石油衍生馏分油范围的物流共混作为共混原料或燃料添加剂以形成可再生馏分油的装置。
应当理解的是,图1中所示的生物质转化***只是可以实现本发明的***的一个例子。本发明可在多种其它***中进行应用,这些***均可以高效和有效地将生物油分离为可再生燃料和/或燃料添加剂。现对图1中所示的示例性生物质转化***进行详细描述。
图1的生物质转化***10包括生物质源12,用于供应生物质原料以供转化为生物油。生物质源12可以是例如漏斗、料仓、有轨车、路面拖车或任何其它可以保持或储存生物质的装置。由生物质源12供应的生物质可以是固体颗粒的形式。生物质颗粒可以是包含纤维素的纤维生物质材料。适合的含纤维素材料的例子包括藻类、造纸废料和/或棉籽绒。在一个实施方案中,生物质颗粒可包括木质纤维素材料。适合的木质纤维素材料的例子包括:林业废料,如木屑、锯屑、纸浆废料和树枝;农业废料,如玉米秸、麦秆和甘蔗渣;和/或能源作物,如桉树、柳枝稷和矮林。
如图1所示,可将来自生物质源12的固体生物质颗粒供应至生物质进料***14。生物质进料***14可以是任何能将固体生物质颗粒进料至生物质转化反应器16的***。在生物质进料***14中,生物质材料会经过若干预处理以利于后续的转化反应。该预处理可以包括干燥、焙烧、烘焙、脱矿物质、蒸汽喷发、机械搅拌和/或它们的任意组合。
在一个实施方案中,在将生物质引入生物质转化反应器16之前,可能需要在生物质进料***14中将生物质与催化剂合并。替代地,可将催化剂直接引入生物质转化反应器16。催化剂可以是新鲜的和/或再生的催化剂。催化剂可以例如包括固体酸如沸石。适合的沸石的例子包括ZSM-5、丝光沸石、β沸石、镁碱沸石和Y沸石。此外,催化剂可以包括超酸。适合的超酸的例子包括氧化锆、氧化钛、氧化铝、氧化硅-氧化铝和/或粘土的磺化、磷酸盐化或氟化形式。在另一个实施方案中,催化剂可以包括固体碱。适合的固体碱的例子包括金属氧化物、金属氢氧化物和/或金属碳酸盐。特别适合的是碱金属、碱土金属、过渡金属和/或稀土金属的氧化物、氢氧化物和碳酸盐。其它适合的固体碱是层状双氢氧化物、混合的金属氧化物、水滑石、粘土和/或它们的组合。在另一个实施方案中,催化剂还可以包括氧化铝如α-氧化铝。
应当注意的是,固体生物质材料通常包含矿物质。可以认识到的是,这些矿物质中的一些如碳酸钾在生物质材料的转化中可以具有催化活性。
生物质进料***14将生物质原料引入生物质转化反应器16。在生物质转化反应器16中,生物质经过转化反应,生成生物油。生物质转化反应器16可促进不同的化学转化反应,如快速热解、慢速热解、液化、气化或酶转化。生物质转化反应器16可以是例如流化床反应器、旋风反应器、烧蚀反应器或提升管反应器。
在一个实施方案中,生物质转化反应器16可以是提升管反应器和转化反应可以是快速热解。更具体地,快速热解可包括催化裂化。这里使用的“热解”是指通过在基本不含氧的气氛中加热原料引发的生物质的热化学转化。在一个实施方案中,在惰性气体如氮气、二氧化碳和/或蒸汽存在下进行热解。替代地,可在还原气体如氢气、一氧化碳、回收自生物质转化过程的不凝气和/或它们的任意组合存在下进行热解。
快速热解的特征在于生物质原料停留时间短和加热快。快速热解反应的停留时间可以是例如小于10秒、小于5秒或小于2秒。快速热解可在200-1000℃、250-800℃或300-600℃的温度下进行。
再参照图1,离开生物质转化反应器16的转化流出物18通常包含气体、蒸气和固体。如这里使用的,转化反应过程中产生的蒸气可互换地称为“生物油”,这是该蒸气冷凝为其液体状态时的常用名称。在本发明的一个实施方案中,在生物质转化反应器16中进行的转化反应生成生物油。该生物油的氧含量可以小于生物油的15、12、10或8wt%。氧含量也可以大于生物油的约0.5、1、3或5wt%。
当在生物质转化反应器16中进行快速热解时,转化流出物18通常包含炭、灰分和/或废催化剂的固体颗粒。可将转化流出物18引入固体分离器20。固体分离器20可以是任何能将固体与气体和蒸气分离的常规装置,例如旋风分离器或气体过滤器。固体分离器20从转化流出物18中脱除大部分固体(例如废催化剂、炭和/或热载体固体)。可将在固体分离器20中回收的固体颗粒22引入再生器24,典型地通过燃烧进行再生。再生后,可将至少一部分热的经再生固体经管线26直接引入生物质转化反应器16。替代地或另外地,可将热的经再生固体经管线28送至生物质进料***14,用于在引入生物质转化反应器16之前与生物质进料合并。
然后,可将离开固体分离器20的基本上不含固体的流体物流30(也称为生物油)引入流体分离器32。在一个实施方案中,优选进入流体分离器32的生物油30未预先经过脱氧过程,例如加氢处理。流体分离器32可以是任何能将生物油30分离为至少轻质馏分34、生物馏分油馏分(组合物)36和重质馏分38的***。用作流体分离器32的适合的***包括例如通过分馏、加热蒸馏、萃取、膜分离、部分冷凝和/或非加热蒸馏进行分离的***。在一些情况下,优选使用加热蒸馏进行分离,其中该加热蒸馏将生物油30的温度提高至100℃以上。如图1所示,可从流体分离器32中脱除不凝气40,和任选地经管线42将它循环至生物质转化反应器16,用作提升气体。
离开流体分离器32的轻质馏分34可具有与石油衍生汽油相当的沸程。离开流体分离器32的生物馏分油组合物36可具有与石油衍生馏分油相当的沸程。
生物馏分油组合物36的沸程可以是:至少75、85、95或100wt%的生物馏分油组合物36在约180-380℃、约190-370℃或约205-355℃的温度下沸腾。重质馏分38的沸程可以是:至少75、85、95或100wt%的重质馏分38在高于380℃、370℃或355℃的温度下沸腾。轻质馏分34的沸程可以是:至少75、85、95或100wt%的轻质馏分34在低于约205℃、190℃或180℃的温度下沸腾。
在一个实施方案中,将进入流体分离器32的生物油30的至少5、15、25或35wt%分离为生物馏分油组合物36。在另一个实施方案中,将进入流体分离器32的生物油30的至少10、20或30wt%分离为轻质馏分34,和将进行分离的生物油30的小于60wt%分离为重质馏分38。
生物馏分油馏分/组合物
生物馏分油组合物36的氧含量可以小于15、12、10、8wt%和/或大于约0.5、1或4wt%。生物馏分油组合物可以包含至少约40或50wt%的无氧烃,和可以含有小于约1或0.5wt%的羰基,和可以含有小于约0.5或0.2wt%的羧酸。
生物馏分油组合物可以含有小于约0.5或小于约0.2wt%的醛,和可以进一步包含约10-40wt%或约20-40wt%的含氧和碳的化合物。含氧和碳的化合物可选自酚、呋喃、酮、醛和它们的组合。
生物馏分油组合物的铜腐蚀测试值优选小于No.3。
可再生馏分油
如图1所示,生物质生产***10可位于石油衍生馏分油源44附近或通过输送***与其连通。石油衍生馏分油源44可以是例如石油炼厂、石油燃料储存设施和/或石油燃料输送***。
可使用馏分油共混***46将来自石油衍生馏分油源44的石油衍生馏分油范围的物流48与至少一部分生物馏分油组合物36和稳定添加剂50合并以生成具有单一澄清相的可再生馏分油组合物52,其中石油衍生馏分油范围的物流48每分子可含有12-25个碳原子。
可再生馏分油组合物可包含:含量为至少5、15或25wt%和/或至多99、98或96wt%的石油衍生馏分油范围的物流48;含量为至少0.5、2、5、25或60wt%的生物馏分油组合物36;和含量为约0.5-25wt%的具有表面活性剂性能的稳定添加剂。
稳定添加剂可包括选自如下的材料:1)亲水亲油平衡值(HLB)为至多8、7或6和/或至少2或3的非离子嵌段共聚物;2)HLB为至多8、7或6和/或至少2或3的非离子均聚物;3)平均HLB为至多8、7或6和/或至少2或3的非离子嵌段共聚物和非离子均聚物的混合物;4)HLB为至多8、7或6和/或至少2或3的非离子表面活性剂;5)脂肪酸甲基酯(FAME);或6)它们的组合。稳定添加剂的例子包括但不限于:Hypermer系列聚合物、Brij系列表面活性剂、异硬脂酸丙二醇酯、Span系列表面活性剂、硬脂酸乙二醇酯、倍半油酸脱水山梨醇酯、硬脂酸甘油酯、卵磷脂系列表面活性剂、油酸脱水山梨醇酯、单硬脂酸脱水山梨醇酯NF、硬脂酸脱水山梨醇酯、异硬脂酸脱水山梨醇、硬脂基聚氧乙烯(2)醚、油基聚氧乙烯(2)醚、月桂酸甘油酯、十六烷基聚氧乙烯(2)醚、PEG系列聚合物表面活性剂、二多羟基硬脂酸酯、硬脂酸甘油酯SE、甲基葡萄糖倍半硬脂酸酯、Atsurf系列表面活性剂和它们的组合。
在其它选择中,石油衍生馏分油范围的物流可以选自常规馏分油、低硫馏分油、经加氢处理的轻质循环油、经加氢处理的直馏瓦斯油、超低硫馏分油、经精炼处理的中间馏分油或它们的组合。
在使用的稳定添加剂包括非离子表面活性剂、非离子嵌段共聚物、非离子均聚物或非离子嵌段共聚物和非离子均聚物的混合物的情况下,为便于处理,优选同时或顺序将稳定添加剂和生物馏分油组合物加入石油衍生馏分油范围的物流,由此形成可再生馏分油。
在稳定添加剂包括FAME的情况下,已经发现通过将生物馏分油组合物与稳定添加剂合并、然后再将这两种组分与石油衍生馏分油范围的物流合并、由此形成可再生馏分油,可以获得明显的操作上的便利。
实施例
实施例1
在反应器出口温度为约650℃下操作的提升管反应器中,在催化剂存在下通过热解转化南方黄松木颗粒而生成低氧生物油。得到的生物油的氧含量为约12wt%,和经过蒸馏得到大于25wt%的沸程低于约345℃的生物馏分油组合物。生物馏分油组合物的组成示于下表1中。
表1
从数据可以看出,生物馏分油组合物质量高、氧含量低、未检出羧酸、和环状化合物/芳族化合物含量大。
实施例2
将一定量的HypermerB241聚合物与商购的超低硫柴油(ULSD)共混以形成第一混合物,然后将它与一定量实施例1的生物馏分油组合物合并以形成可再生馏分油共混物,该共混物中含有97wt%的ULSD、1wt%的HypermerB241和2wt%的生物馏分油。使用超声均化器混合后,可再生馏分油共混物为单一澄清相。
实施例3
将不同量的FAME与不同量实施例1的生物馏分油组合物共混以形成混合物,然后将它与不同量的ULSD合并以形成可再生馏分油共混物,用超声均化器混合所述共混物。全部共混物所得到的单一澄清相示于下表2中。
表2
实施例4
将不同量实施例1的生物馏分油组合物与ULSD共混,使用1wt%的HypermerB246聚合物材料形成含2%生物馏分油(BD)的共混物,HLB值为6;和使用2.5wt%的FAME(获自Houston,TX的HoustonBiodiesel公司)形成含40%生物馏分油(BD)的另一共混物。测试ULSD和各种共混物的多种性质/组分。该测试的结果显示在下表3中。表3还包括两种馏分油石油产物柴油#2S500(D2S500)和燃料油#2(FO#2)的那些性质的规定值。观察到得到的共混物变得澄清和稳定,共混物符合常规馏分油的规格。
表3
从上面表3可以看出,通过将生物馏分油、添加剂和ULSD共混而制成的可再生馏分油的性质符合馏分油燃料的规格。含2wt%生物柴油的可再生馏分油满足柴油#2-S500的规格,而含40%生物柴油的可再生馏分油满足燃料油#2规格(对于40%BD共混物来说,密度和兰氏残碳除外)。
上述本发明的优选形式仅用于举例说明,不应当用于限制性地解释本发明的范围。本领域技术人员可以容易地对上述示例性实施方案做出调整,而不背离本发明的精神。
发明人意图依靠等同原则来确定和评估本发明的合理公平的范围,该范围涉及虽处于如下权利要求书所述发明的字面范围之外但实质上并不与之背离的任何方法和***。

Claims (23)

1.一种生产可再生馏分油的方法,该方法包括:
(a)将生物油分离为至少生物馏分油馏分,其中至少75wt%的所述生物馏分油馏分的沸点为180-380℃,其中所述生物油未预先经过脱氧加氢处理步骤;和
(b)将至少一部分所述生物馏分油馏分与石油衍生馏分油范围的物流和具有表面活性剂性能的稳定添加剂合并,由此生成具有单一澄清相的可再生馏分油,其中所述可再生馏分油包含含量为5-99wt%的所述石油衍生馏分油范围的物流、含量为至少0.5wt%的所述生物馏分油馏分和含量为0.5-25wt%的所述稳定添加剂。
2.权利要求1的方法,其中所述稳定添加剂包括选自如下的材料:1)亲水亲油平衡值(HLB)为至多8的非离子嵌段共聚物;2)HLB为至多8的非离子均聚物;3)平均HLB为至多8的非离子嵌段共聚物和非离子均聚物的混合物;4)HLB为至多8的非离子表面活性剂;5)脂肪酸甲基酯(FAME);或6)它们的组合。
3.权利要求2的方法,其中所述非离子嵌段共聚物、所述非离子均聚物、所述非离子嵌段共聚物和非离子均聚物的混合物以及所述非离子表面活性剂的HLB值均为至少2。
4.权利要求1的方法,其中所述稳定添加剂是FAME。
5.权利要求4的方法,其中所述可再生馏分油包含含量为至少0.5wt%的所述生物馏分油馏分。
6.权利要求4的方法,其中所述可再生馏分油包含含量为至少5wt%的所述生物馏分油馏分。
7.权利要求1的方法,其中所述石油衍生馏分油范围的物流选自常规馏分油、低硫馏分油、经加氢处理的轻质循环油、经加氢处理的直馏瓦斯油、超低硫馏分油、经精炼处理的中间馏分油或它们的组合。
8.权利要求1的方法,其中所述石油衍生馏分油范围的物流包含每分子含有12-25个碳原子的烃。
9.权利要求2的方法,其中所述稳定添加剂包括所述非离子嵌段共聚物、所述非离子均聚物、所述非离子表面活性剂或它们的混合物;和其中同时或顺序将所述稳定添加剂和所述生物馏分油馏分加入所述石油衍生馏分油范围的物流,由此形成可再生馏分油。
10.权利要求2的方法,其中所述稳定添加剂包括FAME;和其中将所述生物馏分油馏分与所述稳定添加剂合并,然后再与所述石油衍生馏分油范围的物流合并,由此形成可再生馏分油。
11.权利要求1的方法,其中将经过步骤(a)分离的所述生物油的至少5wt%分离为所述生物馏分油馏分。
12.权利要求1的方法,其中步骤(a)的分离通过分馏完成。
13.权利要求1的方法,其中所述生物油得自催化剂存在下生物质的热化学转化。
14.权利要求1的方法,其中所述生物油的总氧含量小于15wt%。
15.一种可再生馏分油组合物,该组合物包含含量为5-99wt%的石油衍生馏分油范围的物流、含量为至少0.5wt%的生物馏分油馏分和含量为0.5-25wt%的具有表面活性剂性能的稳定添加剂,其中从生物油中分离所述生物馏分油馏分,其中至少75wt%的所述生物馏分油馏分的沸点为180-380℃,和其中在分离所述生物馏分油馏分之前所述生物油未预先经过脱氧加氢处理步骤。
16.权利要求15的可再生馏分油组合物,其中所述稳定添加剂包括选自如下的材料:1)HLB为至多8的非离子嵌段共聚物;2)HLB为至多8的非离子均聚物;3)平均HLB为至多8的非离子嵌段共聚物和非离子均聚物的混合物;4)HLB为至多8的非离子表面活性剂;5)FAME;或6)它们的组合。
17.权利要求16的可再生馏分油组合物,其中所述非离子嵌段共聚物、所述非离子均聚物、所述非离子嵌段共聚物和非离子均聚物的混合物以及所述非离子表面活性剂的HLB值均为至少2。
18.权利要求16的可再生馏分油组合物,其中所述稳定添加剂是FAME。
19.权利要求18的可再生馏分油组合物,其中所述可再生馏分油组合物包含含量为至少25wt%的所述生物馏分油馏分。
20.权利要求18的可再生馏分油组合物,其中所述可再生馏分油组合物包含含量为至少0.5wt%的所述生物馏分油馏分。
21.权利要求15的可再生馏分油组合物,其中所述石油衍生馏分油范围的物流选自常规馏分油、低硫馏分油、经加氢处理的轻质循环油、经加氢处理的直馏瓦斯油、超低硫馏分油、经精炼处理的中间馏分油或它们的组合。
22.权利要求15的可再生馏分油组合物,其中所述石油衍生馏分油范围的物流包含每分子含有12-25个碳原子的烃。
23.权利要求15的可再生馏分油组合物,其中所述生物油得自催化剂存在下生物质的热化学转化。
CN201180052116.4A 2010-10-29 2011-10-07 可再生生物馏分油的生产 Expired - Fee Related CN103189479B (zh)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US12/915,872 US8377152B2 (en) 2010-10-29 2010-10-29 Production of renewable bio-distillate
US12/915,872 2010-10-29
PCT/US2011/055411 WO2012057988A1 (en) 2010-10-29 2011-10-07 Production of renewable bio-distillate

Publications (2)

Publication Number Publication Date
CN103189479A CN103189479A (zh) 2013-07-03
CN103189479B true CN103189479B (zh) 2015-11-25

Family

ID=45492389

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201180052116.4A Expired - Fee Related CN103189479B (zh) 2010-10-29 2011-10-07 可再生生物馏分油的生产

Country Status (7)

Country Link
US (3) US8377152B2 (zh)
EP (1) EP2633006B1 (zh)
CN (1) CN103189479B (zh)
BR (1) BR112013009843A2 (zh)
CA (1) CA2811646C (zh)
DK (1) DK2633006T3 (zh)
WO (1) WO2012057988A1 (zh)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9447350B2 (en) 2010-10-29 2016-09-20 Inaeris Technologies, Llc Production of renewable bio-distillate
US8377152B2 (en) 2010-10-29 2013-02-19 Kior, Inc. Production of renewable bio-distillate
US9382489B2 (en) 2010-10-29 2016-07-05 Inaeris Technologies, Llc Renewable heating fuel oil
US9315739B2 (en) 2011-08-18 2016-04-19 Kior, Llc Process for upgrading biomass derived products
US10427069B2 (en) 2011-08-18 2019-10-01 Inaeris Technologies, Llc Process for upgrading biomass derived products using liquid-liquid extraction
US9206365B2 (en) * 2012-01-10 2015-12-08 Kior, Llc Fungible bio-oil
US9534181B2 (en) 2012-06-19 2017-01-03 Inaeris Technologies, Llc Method of using renewable fuel composition
US9624446B2 (en) 2012-06-19 2017-04-18 Inaeris Technologies, Llc Low temperature property value reducing compositions
US9303213B2 (en) 2012-07-19 2016-04-05 Kior, Llc Process for producing renewable biofuel from a pyrolyzed biomass containing bio-oil stream
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
DE112014002480T5 (de) * 2013-05-20 2016-03-03 Cabot Corporation Elastomerkomposite, -mischungen und Verfahren zu ihrer Herstellung
EP3033407B1 (en) * 2013-08-12 2019-10-16 Inaeris Technologies, LLC Process for upgrading bio-oil
US20150148478A1 (en) * 2013-11-25 2015-05-28 Kior, Inc. Renewable Non-Carcinogenic Bio Oil-Derived Residue Compositions, and Methods of Making and Using
US20160168481A1 (en) * 2014-12-15 2016-06-16 Uop Llc Methods and apparatuses for co-processing pyrolysis oil
US20160177184A1 (en) * 2014-12-18 2016-06-23 The United States Of America, As Represented By The Secretary Of Agriculture Bio-Oils and Methods of Producing Bio-Oils from Guayule Bagasse and/or Leaves
US9523050B2 (en) 2014-12-18 2016-12-20 Uop Llc Methods for co-processing renewable feedstock and petroleum distillate feedstock
WO2022155166A1 (en) * 2021-01-12 2022-07-21 Rj Lee Group, Inc Additives and methods for improving flow properties of crude oil
WO2023159014A1 (en) * 2022-02-17 2023-08-24 Teal Sales Incorporated Systems and methods for the thermochemical production and refining of hydrocarbon compounds

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1526005A (zh) * 2000-11-08 2004-09-01 Aae�����������޹�˾ 燃料组合物
EP2071005A1 (en) * 2007-12-03 2009-06-17 BIOeCON International Holding N.V. Process for the selective de-oxygenation of biomass
CN101679874A (zh) * 2007-03-08 2010-03-24 维仁特能源***公司 由氧化烃合成液体燃料和化学品

Family Cites Families (42)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4209647A (en) 1978-06-22 1980-06-24 American Can Company Fractionation of oil obtained by pyrolysis of lignocellulosic materials to recover a phenolic fraction for use in making phenol-formaldehyde resins
GB2155034B (en) 1983-07-15 1987-11-04 Broken Hill Pty Co Ltd Production of fuels, particularly jet and diesel fuels, and constituents thereof
CA2009021C (en) * 1990-01-31 2001-09-11 Barry A. Freel Method and apparatus for a circulating bed transport fast pyrolysis reactor system
GB9426066D0 (en) 1994-12-22 1995-02-22 Radlein Desmond S G Method of upgrading biomass pyrolysis liquids for use as fuels and as a source of chemicals by reaction with alcohols
US8232437B2 (en) * 1996-11-18 2012-07-31 Bp Oil International Limited Fuel composition
US5820640A (en) 1997-07-09 1998-10-13 Natural Resources Canada Pyrolysis liquid-in-diesel oil microemulsions
US6172272B1 (en) * 1998-08-21 2001-01-09 The University Of Utah Process for conversion of lignin to reformulated, partially oxygenated gasoline
EP1184443A1 (en) 2000-09-04 2002-03-06 Biofuel B.V. Process for the production of liquid fuels from biomass
US7279018B2 (en) * 2002-09-06 2007-10-09 Fortum Oyj Fuel composition for a diesel engine
US20040111955A1 (en) * 2002-12-13 2004-06-17 Mullay John J. Emulsified water blended fuels produced by using a low energy process and novel surfuctant
JP2007508922A (ja) 2003-10-02 2007-04-12 ミシシッピ・ステイト・ユニバーシティ 廃水処理プラント汚泥からのバイオディーゼル燃料及び他の有用な化学物質の生成
WO2006037368A1 (en) 2004-10-04 2006-04-13 Petroleo Brasileiro S.A.-Petrobras Process for reducing the organic acid content of hydrocarbon feedstocks
US7491858B2 (en) * 2005-01-14 2009-02-17 Fortum Oyj Method for the manufacture of hydrocarbons
EP1719811A1 (en) 2005-05-04 2006-11-08 Albemarle Netherlands B.V. Process for producing liquid hydrocarbons from biomass
NL1030129C2 (nl) 2005-10-06 2007-04-10 Euro Trol Bv Samenstel en werkwijze voor het inbrengen van een dosis van een mengsubstantie in een houder.
BRPI0601403B1 (pt) * 2006-04-17 2015-11-03 Petroleo Brasileiro Sa processo de obtenção de n-parafinas a partir de óleo vegetal
EP1852493A1 (en) 2006-05-05 2007-11-07 BIOeCON International Holding N.V. Hydrothermal treatment of carbon-based energy carrier material
US7901568B2 (en) 2006-05-05 2011-03-08 Kior Inc. Process for converting carbon-based energy carrier material
US7819930B2 (en) 2006-05-15 2010-10-26 University Of Georgia Research Foundation, Inc. Miscible, multi-component, diesel fuels and methods of bio-oil transformation
US20080006520A1 (en) 2006-07-06 2008-01-10 Badger Phillip C Method and system for accomplishing flash or fast pyrolysis with carbonaceous materials
US7977517B2 (en) * 2007-03-08 2011-07-12 Virent Energy Systems, Inc. Synthesis of liquid fuels and chemicals from oxygenated hydrocarbons
US7425657B1 (en) 2007-06-06 2008-09-16 Battelle Memorial Institute Palladium catalyzed hydrogenation of bio-oils and organic compounds
US8158842B2 (en) 2007-06-15 2012-04-17 Uop Llc Production of chemicals from pyrolysis oil
CA2692380A1 (en) 2007-06-29 2009-01-29 Ted R. Aulich Aviation-grade kerosene from independently produced blendstocks
US8202332B2 (en) * 2007-08-01 2012-06-19 Virginia Tech Intellectual Properties Fractional catalytic pyrolysis of biomass
US8545581B2 (en) 2007-08-01 2013-10-01 Virginia Tech Intellectual Properties, Inc. Production of stable biomass pyrolysis oils using fractional catalytic pyrolysis
US8551327B2 (en) 2007-12-27 2013-10-08 Exxonmobil Research And Engineering Company Staged co-processing of biofeeds for manufacture of diesel range hydrocarbons
ES2871871T3 (es) 2008-03-04 2021-11-02 Univ Massachusetts Método para la pirólisis catalítica de biomasa sólida para la producción de hidrocarburos
US8193399B2 (en) 2008-03-17 2012-06-05 Uop Llc Production of diesel fuel and aviation fuel from renewable feedstocks
EP2107100A1 (en) 2008-03-25 2009-10-07 KiOR Inc. Multi-stage biocatalytic cracking process
US8324438B2 (en) 2008-04-06 2012-12-04 Uop Llc Production of blended gasoline and blended aviation fuel from renewable feedstocks
JP2011517470A (ja) 2008-04-06 2011-06-09 ユーオーピー エルエルシー バイオマス由来熱分解油からの燃料および燃料ブレンド成分
US20090253947A1 (en) * 2008-04-06 2009-10-08 Brandvold Timothy A Production of Blended Fuel from Renewable Feedstocks
US8329968B2 (en) 2008-04-06 2012-12-11 Uop Llc Production of blended gasoline aviation and diesel fuels from renewable feedstocks
US8329967B2 (en) 2008-04-06 2012-12-11 Uop Llc Production of blended fuel from renewable feedstocks
US7888540B2 (en) 2008-04-11 2011-02-15 General Electric Company Integrated system and method for producing fuel composition from biomass
US8304592B2 (en) 2008-06-24 2012-11-06 Uop Llc Production of paraffinic fuel from renewable feedstocks
US8288599B2 (en) 2008-06-30 2012-10-16 Kior, Inc. Co-processing solid biomass in a conventional petroleum refining process unit
US8697924B2 (en) * 2008-09-05 2014-04-15 Shell Oil Company Liquid fuel compositions
WO2010033512A1 (en) 2008-09-16 2010-03-25 Regents Of The University Of Minnesota Improved process for preparing bio-oils from biomass
EP2199364A3 (en) 2008-12-10 2010-10-06 KiOR, Inc. Counter-current process for biomass conversion
US8377152B2 (en) 2010-10-29 2013-02-19 Kior, Inc. Production of renewable bio-distillate

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1526005A (zh) * 2000-11-08 2004-09-01 Aae�����������޹�˾ 燃料组合物
CN101679874A (zh) * 2007-03-08 2010-03-24 维仁特能源***公司 由氧化烃合成液体燃料和化学品
EP2071005A1 (en) * 2007-12-03 2009-06-17 BIOeCON International Holding N.V. Process for the selective de-oxygenation of biomass

Also Published As

Publication number Publication date
CA2811646C (en) 2021-01-19
WO2012057988A1 (en) 2012-05-03
US8377152B2 (en) 2013-02-19
CA2811646A1 (en) 2012-05-03
US8454712B2 (en) 2013-06-04
CN103189479A (zh) 2013-07-03
EP2633006A1 (en) 2013-09-04
DK2633006T3 (da) 2019-08-19
US20120266526A1 (en) 2012-10-25
EP2633006B1 (en) 2019-05-22
US8506658B2 (en) 2013-08-13
US20120260564A1 (en) 2012-10-18
BR112013009843A2 (pt) 2016-07-26
US20120017492A1 (en) 2012-01-26
EP2633006A4 (en) 2014-08-13

Similar Documents

Publication Publication Date Title
CN103189479B (zh) 可再生生物馏分油的生产
CN103189480B (zh) 可再生生物汽油的生产
CN103124781B (zh) 可再生生物燃料的制备
US8647398B2 (en) Production of renewable biofuels
US9206365B2 (en) Fungible bio-oil
MX2013009118A (es) Bioaceite estable.
US9617489B2 (en) Liquid bio-fuels
EP3856874A1 (en) Co-processing hydrothermal liquefaction oil and co-feed to produce biofuels
DK3094708T3 (en) Liquid biofuels
Corredores et al. Ramirez Corredores et al.
EP3033407A1 (en) Production of renewable bio-distillate

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
C41 Transfer of patent application or patent right or utility model
TR01 Transfer of patent right

Effective date of registration: 20151116

Address after: Texas USA

Patentee after: KIOR LLC

Address before: Texas in the United States

Patentee before: KIOR, Inc.

CF01 Termination of patent right due to non-payment of annual fee
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20151125