Classifications

• • 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
  • C10G3/00—Production of liquid hydrocarbon mixtures from oxygen-containing organic materials, e.g. fatty oils, fatty acids
  • C10G3/50—Production of liquid hydrocarbon mixtures from oxygen-containing organic materials, e.g. fatty oils, fatty acids in the presence of hydrogen, hydrogen donors or hydrogen generating compounds
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
  • C07C45/45—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by condensation
  • C07C45/48—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by condensation involving decarboxylation
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D19/00—Degasification of liquids
  • B01D19/0068—General arrangements, e.g. flowsheets
• • 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
  • B01J21/06—Silicon, titanium, zirconium or hafnium; Oxides or hydroxides thereof
  • B01J21/063—Titanium; 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
  • B01J23/02—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the alkali- or alkaline earth metals or beryllium
  • B01J23/04—Alkali metals
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
  • C07C49/04—Saturated compounds containing keto groups bound to acyclic carbon atoms
• • 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
  • C10G3/00—Production of liquid hydrocarbon mixtures from oxygen-containing organic materials, e.g. fatty oils, fatty acids
  • C10G3/42—Catalytic treatment
• • 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
  • C10G3/00—Production of liquid hydrocarbon mixtures from oxygen-containing organic materials, e.g. fatty oils, fatty acids
  • C10G3/42—Catalytic treatment
  • C10G3/44—Catalytic treatment characterised by the catalyst used
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
  • C10L1/00—Liquid carbonaceous fuels
  • C10L1/02—Liquid carbonaceous fuels essentially based on components consisting of carbon, hydrogen, and oxygen only
  • C10L1/026—Liquid carbonaceous fuels essentially based on components consisting of carbon, hydrogen, and oxygen only for compression ignition
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
  • C10L1/00—Liquid carbonaceous fuels
  • C10L1/10—Liquid carbonaceous fuels containing additives
  • C10L1/14—Organic compounds
  • C10L1/18—Organic compounds containing oxygen
  • C10L1/185—Ethers; Acetals; Ketals; Aldehydes; Ketones
  • C10L1/1857—Aldehydes; Ketones
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
  • C10M105/00—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
  • C10M105/08—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen
  • C10M105/20—Aldehydes; Ketones
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D2257/00—Components to be removed
  • B01D2257/50—Carbon oxides
  • B01D2257/504—Carbon dioxide
• • 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
  • B01J2523/00—Constitutive chemical elements of heterogeneous catalysts
  • B01J2523/20—Constitutive chemical elements of heterogeneous catalysts of Group II (IIA or IIB) of the Periodic Table
  • B01J2523/22—Magnesium
• • 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
  • B01J2523/00—Constitutive chemical elements of heterogeneous catalysts
  • B01J2523/20—Constitutive chemical elements of heterogeneous catalysts of Group II (IIA or IIB) of the Periodic Table
  • B01J2523/23—Calcium
• • 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
  • B01J2523/00—Constitutive chemical elements of heterogeneous catalysts
  • B01J2523/40—Constitutive chemical elements of heterogeneous catalysts of Group IV (IVA or IVB) of the Periodic Table
  • B01J2523/47—Titanium
• • 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
  • B01J2523/00—Constitutive chemical elements of heterogeneous catalysts
  • B01J2523/40—Constitutive chemical elements of heterogeneous catalysts of Group IV (IVA or IVB) of the Periodic Table
  • B01J2523/48—Zirconium
• • 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
• • 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
  • C10G2300/40—Characteristics of the process deviating from typical ways of processing
  • C10G2300/4081—Recycling aspects
• • 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
  • C10G2400/00—Products obtained by processes covered by groups C10G9/00 - C10G69/14
  • C10G2400/04—Diesel oil
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
  • C10L2270/00—Specifically adapted fuels
  • C10L2270/02—Specifically adapted fuels for internal combustion engines
  • C10L2270/026—Specifically adapted fuels for internal combustion engines for diesel engines, e.g. automobiles, stationary, marine
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
  • C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
  • C10M2207/08—Aldehydes; Ketones
  • C10M2207/085—Aldehydes; Ketones used as base material
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
  • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
  • Y02E50/00—Technologies for the production of fuel of non-fossil origin
  • Y02E50/10—Biofuels, e.g. bio-diesel
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
  • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
  • 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 present invention relates to the field of fuel and base oil production. More specifically the invention relates to a method for producing ketones from a feedstock of biological origin comprising fatty acids and/or fatty acid derivatives in a system comprising one or more ketonisation reactors and use of the ketones for the manufacture of fuel and base oil components.
• Base oils find use for modern engine lubrication technologies.
• High-quality base oil should enable engines to deliver high-level performance and power without compromising fuel economy or environmental standards, and there is a need for renewable sources in the production of base oils and lubricants.
• Oils from biomass contain free fatty acids and/or triglycerides, however, the hydrocarbons' chain lengths in the fatty acids are too short for base oils with the qualities wished for.
• Ketonisation by combining two fatty acids to form a long-chain ketone is an appropriate reaction route for formation of suitable long-chain hydrocarbons applicable also as base oil or diesel fuel components.
• the long chain ketones can readily be hydrogenated to yield straight chain hydrocarbons. These hydrocarbons in turn can be further isomerized to produce various base oil or diesel fuel components.
• the route is based on the following reaction scheme:
• ketonisation may be the first step in e.g. base oil production technology, and it is conducted over a suitable catalyst for the ketonisation process.
• Base oil production technology including the use of a ketonisation reaction is disclosed e.g. in WO 2007/068795, which is incorporated herein for reference.
• the ketonisation step is a critical step in the overall process both for the material and energy efficiency of the process, since the ketone product is subject to further catalytic conversions, such as hydrodeoxygenation and isomerisation, prior to appliance in e.g. base oil.
• the ketonisation step is sensitive to the reactor temperature and it is an endothermic reaction (viz. consumes energy), and vaporisation of certain components, in particular H2O and CO2, further decreases the reactor temperature leading to an adverse effect on the ketonisation process.
• a full scale plant is typically operated at slightly lower temperatures compared to optimal temperature for practical reasons. However, operation at a lower temperature than the optimum requires as compensation a larger amount of catalyst which on its side increases the production of unwanted, heavy by-products, such as trimers.
• the ketonisation reaction requires the use of a catalyst bed. Gas evolution/generation from the ketonisation reaction may cause problems at the catalyst bed due to uneven liquid flows through the catalyst beds, whereby the reaction is further negatively influenced.
• US 2013/0310608 discloses a process for reducing the emission of volatile organic compounds that are produced during the ketonisation of acetic acid to acetone.
• the ketonisation produces a gaseous by-product stream containing carbon dioxide and volatile organic compounds.
• This gaseous by-product stream can be fed to a direct-fired furnace used to heat the ketonisation reaction feed streams where the volatile organic compounds are destroyed by combustion in the furnace.
• the carbon dioxide stream further acts as a diluent for the fuel to the furnace.
• US 2017/324449 discloses a process for producing ketones or hydrocarbons base oil from fatty acids, preferably derived from a biological origin.
• the ketonisation reaction is performed in vapour phase in a decarboxylation-coupling zone wherein the temperature is between 20 and 100 °C above the condensation point of the fatty acid at the partial pressure of the fatty acid in the decarboxylation-coupling zone
• US 6,307,106 discloses a catalytic process for preparing lower unsaturated ketones by reacting the corresponding alpha-beta-unsaturated alcohols with alkyl acetoacetate, and a suitable reactor system for the reaction.
• the object of the present invention is to provide an improved method for producing ketones suitable for manufacture of base oil or diesel components from a feedstock of biological origin.
• Another object is to provide a method for producing ketones suitable for manufacture of base oil or diesel components wherein the adverse effects on the ketonisation reaction of the endothermic temperature drop are handled so as to maintain the reactor temperature within acceptable ranges and to maintain low water concentration in the liquid phase in the reactor.
• Yet another object is to provide a method enabling a high yield of ketone with high fatty acids utilisation without compromising the quality of the base oil or diesel fuel component.
• the present invention relates in a first aspect to a method for producing ketones, suitable for manufacture of base oil or diesel fuel components, from a feedstock of biological origin comprising fatty acids and/or fatty acid derivatives, wherein the feedstock is at least partly in liquid phase, by subjecting the feedstock to a catalytic ketonisation reaction, wherein the ketonisation reaction is carried out in a system comprising one or more ketonisation reactor(s) each comprising at least one ketonisation catalyst bed, further comprising that
• gas comprising CO2 is separated from the effluent exiting a ketonisation reactor whereby the effluent comprising ketones is used either as a feedstock for a further ketonisation reactor or for recovery of ketones from the effluent;
• hydrocarbons such as diesel-range hydrocarbons
• side products which may be returned to the ketonisation or directed to hydro treatment.
• the process does not produce any waste, merely commercially applicable products such as ketones, diesel components and pure C02, and water. It has been observed that the usage of carrier gas accelerates the ketonisation reaction. This is mainly explained by the fact that the flow of carrier gas strips the formed water from the liquid phase to the gas phase side. Water dissolved in the liquid organic phase will inhibit the catalysis of the ketonisation, whereas water in the reactor gas phase - without a direct contact with the catalyst - is harmless.
• the ketonisation reaction is highly sensitive to the reaction temperature, and that the activation energy is about 160 kJ/mol.
• the energetics of ketonisation is endothermic, and the reaction enthalpy, DH, is 30 kJ/mol.
• the combination of these reaction characteristics easily result in an inefficient reactor, as the adiabatic behavior with the progress of reaction will cause the reactor temperature to drop from the entrance of the reactor towards the exit of the reactor.
• the method of the present invention is founded on the observations that in an industrial scale reactor, the mass and heat transfer characteristics need to be upgraded by reaction engineering to improve the activity and selectivity of the ketonisation reaction.
• the key drivers were found to be the following:
• the present invention relates to a system for producing ketones, suitable for manufacture of base oil components, from a feedstock of biological origin comprising fatty acids and/or fatty acid derivatives by subjecting the feedstock to a catalytic ketonisation reaction, wherein
• the system comprises one or more ketonisation reactors (A', B') each comprising a ketonisation at least one catalyst bed (G'), means for heating, preferably an oil heater, inlet means for the feedstock ( ) and outlet means for the effluent (2', 4') exiting a ketonisation reactor;
• the one or more ketonisation reactors each further comprises inlet means for carrier gas streams (5', 6'), outlet means for separated gas streams comprising CO2 (8', 10'); and wherein
• the system further comprises one or more gas-liquid separators (D', E') for separating CO2 in the separated gas streams (8', 10') from H2O vapour, unreacted fatty acids and/or fatty acid derivatives, and/or volatile organic compounds, and means (F') for recirculating and optionally compressing the separated CO2; and optionally
• the third aspect of the invention relates to the use of a gas comprising CO2 as a carrier gas stream in a ketonisation reaction, wherein the gas comprising CO2 has been produced in a catalytic ketonisation reaction producing ketones, suitable for manufacture of base oil components, from a feedstock of biological origin comprising fatty acids and/or fatty acid derivatives in one or more ketonisation reactors each comprising a ketonisation catalyst bed, and wherein the gas has been separated from the effluent exiting a ketonisation reactor and recycled.
• the fourth aspect of the invention it relates to the use of ketones obtainable by a method of the invention for the manufacture of base oil or base oil components.
• the selectivity for the target ketone is high, preferably in the range of 95 mole-%, or even higher. This may be explained by the ketonisation being a second order reaction, favored by the presence of concentrated reactant. Therefore, in one embodiment of the invention in all its aspects the feedstock is at least partly in liquid phase.
• fatty acid is well-known to the skilled person and as used herein characterises a carboxylic acid consisting of a hydrocarbon chain and a terminal carboxyl group, in particular any of those carboxylic acids occurring as esters in fats and oils.
• the feedstock of biological origin is to be understood as a feedstock which comprises free fatty acids or fatty acid derivatives, such as esters, amides, aldehydes, alcohols, anhydrides, metal salts, or mixture thereof, the fatty acids having 4 or more C atoms, and suitable for the manufacture of base oil components.
• Most fatty acids of plant or animal origin are straight-chain compounds, which most frequently contain an even number of carbon atoms, such as 6 to 24 C atoms, e.g. 8, 10, 12, 14, 16, 18, 20, or 22 C atoms, and usually no or only trace amounts of odd-numbered fatty acids.
• the fatty acid may be saturated or unsaturated.
• Fatty acid esters are e.g.
• fatty acid glycerols The ketonisation reaction requires free fatty acids, and degraded or low-value biological oils are typically mixtures of free fatty acids and fatty acid glycerols, such as triglycerides or partial glycerides.
• the major part of the free fatty acids and fatty acid esters may, for example, be considered to be more than 50 wt %, such as more than 70 wt%, more than 90 wt%.
• Renewable diesel fuel in the context of the present invention is to be understood as deriving from unreacted fatty acids or ketonisation product of reacted fatty acids of biological origin which have been hydro treated into paraffins.
• the paraffins are typically long chain hydrocarbons which in connection with the present invention mean that the average carbon chain length is at least 7 atoms.
• Renewable base oil in the context of the present invention is to be understood as deriving from ketonisation of fatty acids of biological origin to form ketones.
• the ketones are typically long chain ketones which in connection with the present invention means that the ketone average chain length is 7 or more C-atoms.
• base oil components contain carbon 14 C isotope, it is an indication of its use as renewable base oil as disclosed in WO 2007/068799 which is incorporated herein for reference.
• Ketonisation reactor is a continuously operated pressure vessel where ketonisation reaction is carried out over a fixed bed of ketonisation catalyst.
• Figure 1 shows a block diagram for a system for producing ketones according to the invention comprising three ketonisation reactors, two gas-liquid separators and a compressor.
• Figure 2 shows a block diagram for a system for producing ketones according to the invention comprising two ketonisation reactors, two gas-liquid separators and a compressor.
• ketones suitable for manufacture of base oil or diesel fuel components ketones produced from fatty acid containing feed wherein the fatty acid carbon chain length is 4 or more C atoms, preferably at least 6 C atoms, resulting in a ketone comprising at least 7 C atoms, preferably at least 11 C atoms, in length when ketonised.
• These hydrocarbons are suitable for the manufacture of diesel fuel components having the lower carbon number range, typically from C7 to C20; and base oil components having the higher carbon number range, such as from Cll upwards.
• the feedstock used according to the invention is of biological origin and comprises fatty acids and/or fatty acid derivatives, such as esters, amides, aldehydes, alcohols, anhydrides, metal salts, or mixture thereof.
• the fatty acid may be saturated or unsaturated, and the derivatives may for example be fatty acid esters, including glycerols selected from mono-, di-, and triglycerides, fatty acid amides and fatty alcohols.
• the feedstock of biological origin may e.g. be selected from
• any kind of fats any kind of waxes, plant fats, plant oils, plant waxes; animal fats, animal oils, animal waxes, fish fats, fish oils, fish waxes, and
• fatty acids or free fatty acids obtained from plant fats, plant oils, plant waxes; animal fats, animal oils, animal waxes; fish fats, fish oils, fish waxes, and mixtures thereof by hydrolysis, transesterification, or pyrolysis, and
• esters obtained from plant fats, plant oils, plant waxes; animal fats, animal oils, animal waxes; fish fats, fish oils, fish waxes, and mixtures thereof by transesterification, and
• metal salts of fatty acids obtained from plant fats, plant oils, plant waxes; animal fats, animal oils, animal waxes; fish fats, fish oils, fish waxes, and mixtures thereof by saponification, and v) anhydrides of fatty acids from plant fats, plant oils, plant waxes; animal fats, animal oils, animal waxes; fish fats, fish oils, fish waxes, and mixtures thereof, and
• esters obtained by esterification of free fatty acids of plant, animal, and fish origin with alcohols and
• fatty alcohols or aldehydes obtained as reduction products of fatty acids from plant fats, plant oils, plant waxes; animal fats, animal oils, animal waxes; fish fats, fish oils, fish waxes, and mixtures thereof, and
• the feedstock is at least partly in liquid phase.
• the feedstock is at least 60 wt-% in liquid phase, preferably at least 65 wt-%, more preferably at least 70 wt-%, at least 75 wt-%, at least 80 wt-%, or at least 90 wt-% in liquid phase, and most preferred 100 wt-% in liquid phase.
• the feedstock of biological origin may comprise saturated free fatty acids and/or saturated fatty acid derivatives, such as esters, amides, aldehydes, alcohols, anhydrides, metal salts, or mixture thereof, preferably fatty acid glycerols.
• the feedstock of biological origin may comprise saturated free fatty acids and/or saturated fatty acid esters having an average carbon chain length of from C 4 to C , preferably having an average carbon chain length of from C 6 to C .
• the ketonisation catalyst bed may comprise a ketonisation catalyst which is a metal oxide catalyst.
• Typical metals include Na, Mg, K, Ca, Sc, Cr, Mn, Fe, Co, Ni, Cu, Ti, Sr, Y, Zr, Mo, Rh, Cd, Sn, La, Pb, Bi and rare earth metals.
• the metals are selected from the list consisting of one or more of: Ti, Mn, Mg, Ca, and Zr containing metal oxide catalyst, most preferably the ketonisation catalyst is a Ti containing metal oxide catalyst.
• the metal oxides may be on a support. Typical supports are laterite, bauxite, titanium dioxide, silica and/or aluminium oxide.
• the most important parameters to control are the WHSV, viz. catalyst loading, and the feedstock temperature.
• the temperature in the feedstock may be selected as at least 330 °C, preferably at least 340 °C, more preferably at least 350 °C, most preferably at least 355 °C, and most preferred 360-365 °C, in particular if the carbon number of the feed is 6 or more.
• the liquid feed flow rate, WHSV may be selected from 0.1 to 10 h 1 , preferably from 0.2 to 5 h 1 , more preferably from 0.3 to 3 h 1 , most preferably from 0.5 to 1 h
• the pressure in a ketonisation reactor may be selected as at least 1000 kPa, preferably at least 1200 kPa, more preferably at least 1300 kPa, even more preferably at least 1500 kPa, most preferably at least 2000 kPa, or most preferred at least 2500 kPa.
• the pressure is from 500 to 5000 kPa, major part of the acid is in liquid form.
• the pressure is preferably from 1500-2000 bar, whereas for the diesel fuel component a pressure from 1000 to 5000 kPa is applicable.
• the ketonisation reaction is carried out in a system comprising two or more ketonisation reactors in series each comprising a ketonisation catalyst bed; further comprising that
• the gas comprising CO2 is separated from the effluent exiting each ketonisation reactor leaving a degassed effluent which is subsequently introduced into the next ketonisation reactor together with a further carrier gas stream comprising CO2;
• the separated gas streams comprising CO2 are recycled and used as the carrier gas stream in one or more of the ketonisation reactor(s).
• the pressure in each ketonisation reactor following the first ketonisation reactor may be adjusted to be lower than the pressure in the preceding ketonisation reactor. By selecting the pressures in a decreasing series, the pressure difference drives the liquid stream without pumping.
• the catalyst loading in the catalyst bed in each ketonisation reactor following the first ketonisation reactor is higher than the catalyst loading in the first ketonisation reactor, preferably at least 50 % higher.
• the catalyst loading is e.g. preferably at least 10 % higher in the second reactor, and/or preferably at least 50 % higher in the third reactor, if three reactors are included in the series.
• the ketonisation system may comprise at least two ketonisation reactors, and the effluent exiting a ketonisation reactor and separated from gas comprising CO2 may be heated before introduction into a subsequent ketonisation reactor.
• separated gas streams comprising CO2 may be purified before recycling and recovered in a separation process comprising steps of separating CO2 and H2O vapour from unreacted fatty acids, fatty acids derivatives and volatile organic compounds, and/or separating substantially pure CO2, such as at least 98 % pure, preferably 99 % pure CO2 , more preferably 99.5 %, most preferably 99.9 % pure CO2, from the waste water, and the unreacted fatty acids and fatty acids derivatives are optionally recycled to a ketonisation reactor.
• the purification of the CO2 before re-feeding it to the reactor makes the gas dry and enhances ketonisation reaction rate and also assists in avoiding enrichment of other light products in the recycle loop.
• separated gas comprising CO2 may be subjected to purification, such as by cooling, and optionally further purification, and/or the recovered purified gas may dried before recycling it to a ketonisation reactor.
• substantially pure CO2 may be recovered and subjected to compression, optionally under heating, before recycling it to a ketonisation reactor.
• the heat generated by the cooling may be used for compression under heating of the substantially pure CO2 .
• the method may further comprise a hydrodeoxygenation step, an optional isomerisation step, and optional hydrofinishing steps.
• the hydrodeoxygenation step is required if base oil components are to be produced.
• the hydrodeoxygenation step, and isomerisation step, if applied, may either be done simultaneously or in sequence.
• the product is a deoxygenated and optionally isomerised base oil stream comprising renewable base oil.
• the hydrodeoxygenation reaction is done in the presence of hydrogen gas and may be performed in the presence of a hydrodeoxygenation catalyst, such as C0M0, NiMo, NiW, CoNiMo on a support, for example an alumina support, zeolite support, or a mixed support.
• a hydrodeoxygenation catalyst such as C0M0, NiMo, NiW, CoNiMo on a support, for example an alumina support, zeolite support, or a mixed support.
• the hydrodeoxygenation step may for example be conducted at a temperature in the range from 250 to 400 °C, and at a pressure in the range from 20 to 80 barg, a WHSV in the range from 0.5 to 3 h-1, and a H2/0N ratio of 350- 900 nl/l, using a catalyst, such as NiMo, optionally on a alumina support.
• the product of the hydrodeoxygenation step may be subjected to an isomerization step in the presence of hydrogen and an isomerization catalyst.
• the isomerisation catalyst may be a noble metal bifunctional catalyst such as a for example Pt-SAPO or Pt-ZSM-catalyst or NiW.
• the isomerization step may for example be conducted at a temperature of 250-400 °C and at a pressure of 10-60 barg.
• the isomerisation step may for example be conducted at a temperature of 250- 400 °C, at a pressure of between 10 and 60 barg, a WHSV of 0.5 - 3 h-1, and a H2/oil ratio of 100- 800 nl/l.
• the hydrodeoxygenation and hydroisomerisation steps may be done in a single step on the same catalyst bed using a single catalyst for this combined step, e.g. NiW, or a Pt catalyst, such as Pt/SAPO in mixture with a Mo catalyst on a support, e.g. NiMo on alumina.
• a single catalyst for this combined step e.g. NiW
• a Pt catalyst, such as Pt/SAPO in mixture with a Mo catalyst on a support, e.g. NiMo on alumina.
• the product is stabilised by a further hydrogenation step.
• the hydrofinishing step may be applied to stabilise the product and involves e.g. hydrogenation of double bonds or aromatic compounds that are present after the ketonisation reaction and the following, optional, hydrodeoxygenation and isomerisation steps.
• the hydrofinishing step may be conducted at a temperature below 300 °C, and a pressure between 100 and 200 barg.
• the WHSV may for example be 0.5 - 3.0 h-1, and the H2/0M ratio may for example be 100-500 nl/l.
• this aspect of the invention may further comprise means for purifying the separated CO2 to a substantially pure CO2 gas, preferably at least 98 % pure, more preferably 99 % pure, even more preferably 99.5 % pure, most preferably 99.9 % pure CO2.
• system according to the present invention may comprise two, three or four ketonisation reactors, preferably in series.
• the system may comprise three ketonisation reactors (A, B, C), preferably in series, each comprising one or more ketonisation catalyst bed(s) (G), means for heating, inlet means for the feedstock (1) and outlet means for the effluent (2, 3, 4) exiting a ketonisation reactor; wherein
• the three ketonisation reactors each further comprises inlet means for a carrier gas stream (5, 6, 7), outlet means for separated gas streams comprising CO2 (8, 9, 10) ; and wherein
• the system further comprises one or more gas-liquid separators (D, E) for separating CO2 in the separated gas streams (8, 9, 10) from H2O vapour, unreacted fatty acids and/or fatty acid derivatives, and/or volatile organic compounds, and means (F) for recirculating and optionally compressing the separated CO2; and optionally
• one or more ketonisation reactor(s) is a trickle bed reactor.
• system may further comprise means for purification of gas comprising CO 2 , such as means for separation CO 2 and/ H 2 O vapour from volatile organic compounds.
• a gas comprising CO 2 as a carrier gas stream have the effect of enhancing the gas flow within a ketonisation reactor comprising a ketonisation catalyst bed wherein a feedstock of biological origin comprising fatty acids and/or fatty acid derivatives is subjected to a ketonisation reaction.
• enhancing is meant that a more uniform gas flow pattern is allowed throughout the reaction zone.
• the reactor has both CO 2 recycle gas and a liquid feedstock phase present in the reactor inlet, there will be a continuous gas flow through the reactor. This will prevent maldistribution of concentration gradients typically due in single phase reactor with gas evolution during reaction.
• the separated gas comprising CO 2 has been purified and recovered in a separation process comprising steps of separating CO 2 from H 2 O vapour and/or volatile organic compounds and optionally separated as substantially pure CO 2 from the waste water. Part of CO 2 may be retrieved as a product before recycling. This CO 2 is quite pure.
• separated gas comprising CO 2 has been subject to purification, e.g. by cooling, an optionally further purification, and/or the recovered purified gas has been dried before recycling to a ketonisation reactor.
• substantially pure CO 2 has been recovered and subjected to compression, optionally under heating, before recycled to a ketonisation reactor.
• ketones obtainable by a method of the invention for the manufacture of base oil components or for intermediate material for production of base oil components.
• Base oils may further be used to manufacture products including lubricants, motor oil and metal processing fluids.
• the base oil affects many parameters of their endproducts or application such as the viscosity, oxidation stability, volatility, cold flow properties such as pour point, and viscosity index.
• Base oils which can be manufactured from ketones obtained according to the present invention fulfil the requirement of Group III of The American Petroleum Institute (API) which divides base oils into five main groups.
• Groups I to III are petroleum base oil of varying qualities.
• Figure 1 shows a block diagram for a system for producing ketones according to the invention comprising three ketonisation reactors, two gas-liquid separators and a compressor.
• Figure 2 shows a block diagram for a system for producing ketones according to the invention comprising two ketonisation reactors, two gas-liquid separators and a compressor.
• the ketonisation catalyst beds (G) include a suitable ketonisation catalyst, such as a Ti containing metal oxide catalyst.
• the first reactor (A) is loaded with a certain amount of the catalyst
• the second reactor (B) is loaded with a higher amount of the catalyst than reactor A
• the third reactor (C) is loaded with a higher amount of catalyst than reactor B.
• the reaction temperature is the same, e.g. from 330-365 °C, in all reactors (A, B, C). Heating of feedstock 1 and intermediate liquid streams (2, 3) is effectuated with e.g. an oil heater.
• the inlet pressure in the three reactors (A, B, C) declines as the feed passes the three reactors, so that the pressure in reactor A is higher than the inlet pressure in reactor B, which pressure is again higher than the inlet pressure of reactor C; the inlet pressures are e.g. at least 1000 kPa in the reactors.
• the target products of the ketonisation are ketones having an average chain length of C2 n -i.
• the feedstock 1 is led to reactor A by the inlet means and with a suitable liquid feed flow rate. At the same time a flow (5) of CO2 is led as carrier gas to reactor A.
• the effluent (2) leaving reactor A comprises ketones produced by the ketonisation reaction and CO2 .
• CO2 is separated from the effluent (2), is recovered and lead as a gas stream (8) to a first gas- liquid separator (D).
• the remaining part of effluent 2, free of CO2 is lead to reactor B, and at the same time a flow (6) of CO2 is led as carrier gas to reactor B.
• the effluent (3) leaving reactor B also comprises ketones produced by the ketonisation reaction and CO2 .
• CO2 is separated from effluent 3 as described for liquid 2, is recovered and lead as a gas stream (9) to the first gas-liquid separator (D).
• Each gas stream (8, 9, 10) recovered from the reactors effluents (2, 3, 4) is subjected to cooling and lead to the gas-liquid separator D.
• the separation in the gas-liquid separator D leaves a gas flow comprising CO2 and H2O vapor which is lead to a second separator (E).
• CO2 is recovered in separator E and purified to a substantially pure CO2 stream (12).
• CO2 stream 12 is compressed in a compressor (F) before it is used as carrier gas stream to be used in one of the reactors (A, B, C).
• Liquid streams from separator E comprised water and a separate minor stream of organic compounds suitable for diesel.
• Heat released by cooling of the gas streams (8, 9, 10) is partly utilised for re-heating of compressed C0 2 .
• the ketonisation catalyst beds (G') include a suitable ketonisation catalyst.
• the first reactor (A') is loaded with a certain amount of catalyst
• the second reactor (B') is loaded with a higher amount of catalyst than reactor A'.
• the reaction temperature is the same, e.g. from 330-365 °C, in both reactors (A', B'). Heating of the feedstock 1 and the intermediate liquid stream (2') is effectuated with e.g. an oil heater.
• the inlet pressure in the reactors (A', B') declines as the feed passes the two reactors, so that the pressure in reactor A' is higher than the inlet pressure in reactor B'; the inlet pressures are e.g. at least 1000 kPa in the reactors.
• the target products of the ketonisation are ketones having an average chain length of C2 n -i.
• the fatty acid feedstock is led to reactor A' by the inlet means and with a suitable liquid feed flow rate. At the same time a flow (4) of CO2 is led as carrier gas to reactor A'.
• the effluent (2') leaving reactor A' comprises ketones produced by the ketonisation reaction and CO2 .
• CO2 is separated from effluent 2', is recovered and lead as a gas stream (8') to a first gas-liquid separator (D').
• the remaining part of effluent 2', free of CO2 , is lead to reactor B', and at the same time a flow (6') of CO2 is led as carrier gas to reactor B'.
• the effluent (4') leaving reactor B' also comprises ketones produced by the ketonisation reaction and CO2 .
• CO2 is separated from effluent 4' as described for liquid 2', is recovered and lead as a gas stream (10') to gas-liquid separator D'. Separation of the gas stream (10') from effluent 4' leaves the target ketones for recover and further treatment.
• Each gas stream (8', 10') recovered from the reactor effluents (2', 4') are subjected to cooling and lead to the gas-liquid separator D'.
• gas-liquid separator D' leaves a gas flow comprising CC ⁇ and H2O which is lead to a second separator (E').
• CO2 is recovered in separator E' and purified to a substantially pure CO2 stream (12'). Thereafter the CO2 stream 12' is compressed in the compressor (F') before it is used as carrier gas stream to be used in one of the reactors (A',
• Heat released by cooling of the gas streams (8, 10') is partly utilised for re-heating of compressed C0 2 .
• Ci 6 fraction of palmitic acid was used as feedstock in a design wherein the reaction was conducted in a trickle bed system comprising three reactors (A, B, C) in series.
• the ketonisation catalyst beds (G) included a K2O/T1O2 catalyst; loaded as 13,000 kg in the first reactor, 14,000 kg in the second reactor, and 22,000 kg in the third reactor.
• the target product of the ketonisation of Ci 6 acids is C3i-ketones.
• the feed temperature was 350 °C in all reactors (A, B, C).
• the inlet pressure in the three reactors was 1700 kPa in the first reactor (A), 1500 kPa in the second reactor (B), and 1300 kPa in the third reactor (C).
• the palmitic acid feedstock (1) was led to the first reactor (A) by the inlet means.
• the liquid feed flow rate was 20,000 kg/h.
• the CO2 flow (5, 6, 7) was 15,000 kg/h.
• the normal boiling point of palmitic acid is around 351°C, and 1000 kPa was considered as the minimum process pressure.
• CO2 was used as carrier gas and was led to each of the reactors (A, B, C) as the inlet carrier gas streams (5, 6, 7).
• the CO2 produced by the ketonisation reaction in each reactor was separated from the effluents from each reactor (2, 3, 4) and recovered and led as the gas streams (8, 9, 10) to the gas-liquid separators (D, E).
• the first separator (D) CO2 and H2O vapors were separated from liquid organics carried over, mainly unreacted feedstock, and the liquid separated in this separator (11) was recycled to the third reactor (C).
• the gas stream from separator D was led to a second separator (E) wherein CO2 was recovered and purified to a substantially pure CO2 stream and compressed in the compressor (F) before it was used as carrier gas stream to be used in each of the reactors (A, B, C).
• Liquid streams from separator E comprised water and a separate minor stream of organic compounds suitable for diesel.
• the major part of pure CO2 exiting separator E was lead to a compressor, whereas a part of CO2 (equal to the amount produced as side product of ketonisation) is cleaved to a substantially pure CO2 product.
• the feedstock (1) and intermediate liquid streams (2, 3) were heated to the operating temperature of 350 °C with an oil heater.
• the gas streams (8, 9, 10) were subjected to cooling to 272 °C prior to the separation in the first separator (D), and the released heat is partly utilised for re-heating of the compressed CO2. Additional heating and cooling was also required for these streams, implemented as an air cooler operating at 200 °C for additional cooling of the gas streams.
• a water cooler operating at 40 °C was used for the further cooling between the two separators (D, E).
• the results show that the ketonisation process can be implemented with a high yield of the target ketone.
• the present example includes three trickle-bed-reactors in series, the stripping of water and the re-heating of the liquid intermediate product stream after reactors A and B.
• the total base oil precursor yield is 85 weight% out of the theoretical 87.9%.
• the only side products are a minor amount of diesel precursors, water and CO2 .
• the base case assumes 20,000 kg/h feedstock when operating with the temperature of 350 °C and feedstock pressure of 1800 kPa.
• CO2 is used as a carrier gas in the process, recycled, and the amount generated by ketonisation can be recovered in 99.99% purity and considered as another product (1710 kg/h).
• the total amount of CO2 flow rate is 15,000 kg/h.
• Table 3 provides data for the heat exchangers, the pumps and the compressor.
• the cooling of the reactor gas effluent (-686 kW) provides a part of the heat required for the CO2 reheating (686 kW) in an integrated exchanger.
• the inventors also tested appropriate catalyst loadings for a fresh catalyst for the feed temperatures 340, 345 and 350 °C for reaching an acceptable base case performance.
• the conditions tested are indicated in table 5.
• the feed temperature/catalyst loading combinations leading to a high, viz. >83 wt.-% out of theoretical 87.9 wt.-%, base oil precursor yield is indicated.
• the number of required reactors depends on the production capacity and the target yields. For the base case operation, 3-reactor-process configuration is optimal. For smaller production capacities a 2-reactor-process configuration, displayed in Figure 2, is sufficient for providing a good ketone yield.
• the adiabatic temperature drop in the reactors is limited to ten degrees of centigrade, which determines the reactor sizing i.e. catalyst loadings. Qualitatively the operations are equivalent to those described in example 1.

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