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    • 专利摘要:

    公开号:FI20176135A1
    申请号:FI20176135
    申请日:2017-12-19
    公开日:2019-06-20
    发明作者:Jaana Kanervo；Sami Toppinen；Pekka Nurmi
    申请人:Neste Oyj；
    IPC主号:
    专利说明:

    Method for producing ketones for fuel and oil applications
    Technical Field
    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.
    Background
    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 15 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 20 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:
    Fatty acid + Fatty acid => Ketone + CO2 + H2O (ketonisation reaction)
    Ketone + 2 H2 => n-Parafin + H2O (hydrodeoxygenation reaction) n-Parafin => i-Parafin (isomerisation reaction)
    Thus, ketonisation may be the first step in e.g. base oil production technology, and it is conducted 30 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 35 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 40 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.
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    Furthermore, the water produced during the ketonisation reaction inhibits the ketonisation process.
    Finally, the ketonisation reaction requires the use of a catalyst bed. Gas evolution/generation 5 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.
    Therefore, there is a need for enhancing the ketonisation step in the base oil production with the aim of reducing the disadvantageous effects of the endothermic reaction and the water 10 production.
    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 15 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.
    The object of the present invention is to provide an improved method for producing ketones 20 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 25 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.
    These objects are fulfilled with the method of the present invention.
    Summary of the Invention
    Accordingly, 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 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 • the feedstock is introduced into a ketonisation reactor together with a carrier gas stream comprising CO2;
    • 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; and
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    20176135 prh 19-12-2017 • the separated gas comprising CO2 is recycled and used in the carrier gas stream in a ketonisation reactor.
    With the present invention it is possible to obtain at least one of the following advantages:
    o To maintain the operation temperature within an acceptable range despite of the endothermic nature of the ketonisation reaction;
    o To have high yield for target ketone, especially by controlling the adiabatic decrease in the temperature by dividing the reactor into more than one or several units and providing intermediate heating for the units;
    o To increase the yield further by stripping liquid water into gas phase using carrier gas;
    o To avoid the need for additional separations, as the CO2 formed during the ketonisation reaction may also be used as the carrier gas;
    o To have uniform and predictable liquid and gas flow distribution in the reactors, especially in trickle reactors, by the use of the carrier gas; and o To produce pure CO2, the amount of which corresponds to the amount of gas forming in the ketonisation reaction; and o To produce hydrocarbons, such as diesel-range hydrocarbons, as side products which may be returned to the ketonisation or directed to hydro treatment.
    Essentially, the process does not produce any waste, merely commercially applicable products such as ketones, diesel components and pure CO2, 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.
    It has been found, in connection with the present invention, that the ketonisation reaction is highly sensitive to the reaction temperature, and that the activation energy is about 160 kJ/mol. On the other hand, the energetics of ketonisation is endothermic, and the reaction enthalpy, ΔΗ, is 30 kJ/mol. The combination of these reaction characteristics easily result in an inefficient 15 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. Theoretically, it would be advantageous to run the reaction at as high temperature as possible; however the practical limitations are unavailability of economic heating media and possible decay of organic compounds at elevated temperatures.
    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:
    o Usage of carrier gas is required to strip the formed water during the ketonisation reaction;
    o Concentrated solution of reactants need to be in good contact with catalyst; and/or
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    20176135 prh 19-12-2017 o Reasonably high reactant feed temperature and a good control of adiabatic temperature drop is required; and/or o Suppression of side reactions is to be achieved by avoiding excessive contact time and catalyst overloading.
    Potential process configurations are numerous, whereas the preferred alternatives were found to be the ones presented with the present invention. From the energy consumption point of view, excessive temperature or pressure changes are to be avoided in order to minimize the operating expense of heat exchanger, pumping and compressor. Feasible WHSV should be low, but 10 maximized within the yield target and other boundary conditions. The feed temperature vs.
    WHSV (Weight Hourly Space Velocity i.e. mass flow/catalyst mass) combination was found to be the key for tuning the yield to an acceptable level.
    In the second aspect of the present invention, it 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 (F), means for heating, preferably an oil heater, inlet means for the feedstock (1) and outlet means for the effluent (2, 3) exiting a ketonisation reactor; wherein • the one or more ketonisation reactors each further comprises inlet means for carrier gas streams (4, 5), outlet means for separated gas streams comprising CO2 (6, 7); and wherein • the system further comprises one or more gas-liquid separators (C, D) for separating CO2 in the separated gas streams (5, 7) from H2O vapour, unreacted fatty acids and/or fatty acid derivatives, and/or volatile organic compounds, and means (E) for recirculating and optionally compressing the separated CO2; and optionally • recycling means for liquid comprising unreacted fatty acids and/or fatty acid derivatives (8) and outlet means for separated CO2 (9).
    In the third aspect of the invention, it 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.
    In 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.
    It has also been observed that if the fatty acid is in the liquid phase, the selectivity for the target 15 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.
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    Therefore, in one embodiment of the invention in all its aspects the feedstock is at least partly in liquid phase.
    Definitions
    Fatty acids
    The term 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.
    Feedstock
    In the context of the present invention 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 more than 50 wt.-%, such as more than 70 wt.-%, more than 90 wt.-%.
    Renewable diesel fuel
    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
    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.
    When base oil components contain carbon 14C 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
    Ketonisation reactor is a continuously operated pressure vessel where ketonisation reaction is carried out over a fixed bed of ketonisation catalyst.
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    Brief Description of the Drawing
    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.
    Detailed Description of the Invention
    In describing the embodiments of the invention specific terminology will be resorted to for the sake of clarity. However, the invention is not intended to be limited to the specific terms so selected, and it is understood that each specific term includes all technical equivalents which operate in a similar manner to accomplish a similar purpose.
    When describing the embodiments of the present invention, the combinations and permutations of all possible embodiments have not been explicitly described. Nevertheless, the mere fact that certain measures are recited in mutually different dependent claims or described in different embodiments does not indicate that a combination of these measures cannot be used to 20 advantage. The present invention envisages all possible combinations and permutations of the described embodiments.
    The terms comprising, comprise and comprises herein are intended by the inventors to be optionally substitutable with the terms consisting of, consist of and consists of, respectively, 25 in every instance.
    By the expression ketones suitable for manufacture of base oil or diesel fuel components are meant 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 30 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 first aspect of the invention
    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 40 acid amides and fatty alcohols.
    The feedstock of biological origin may e.g. be selected from
    i) 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 ii) fatty acids or free fatty acids obtained from plant fats, plant oils, plant waxes; animal fats,
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    20176135 prh 19-12-2017 animal oils, animal waxes; fish fats, fish oils, fish waxes, and mixtures thereof by hydrolysis, transesterification, or pyrolysis, and iii) 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 iv) 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 vi) esters obtained by esterification of free fatty acids of plant, animal, and fish origin with alcohols, and vii) 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 viii) recycled food grade fats and oils, and fats, oils and waxes obtained by genetic engineering, ix) dicarboxylic acids or polyols including diols, hydroxyketones, hydroxy aldehydes, hydroxycarboxylic acids, and corresponding di- or multifunctional sulphur compounds, corresponding di- or multifunctional nitrogen compounds,
    x) compounds derived from algae, xi) mixtures of said feeds of biological origin.
    In a first embodiment of this aspect of the invention the feedstock is at least partly in liquid phase. Preferably, 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.
    In a second embodiment 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.
    In any of the above embodiments 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 C4 to C24, preferably having an average carbon chain length of from C6to C24.
    In any of the above embodiments in the ketonisation reaction 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. Preferably, 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.
    In designing and controlling the ketonisation performance at the catalyst beds inside the ketonisation reactors, the most important parameters to control are the WHSV, viz. catalyst loading, and the feedstock temperature.
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    Thus, in any of the above embodiments 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.
    In any of the above embodiments the liquid feed flow rate, WHSV, may be selected from 0.1 to 10 h1, preferably from 0.2 to 5 h1, more preferably from 0.3 to 3 IT1, most preferably from 0.5 to 1 h1.
    In any of the above embodiments 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. When the pressure is from 500 to 5000 kPa, major part of the acid is in liquid form. For enhancing the base oil formation, the pressure is preferably from 1500-2000 bar, whereas for the diesel fuel component a pressure from 1000 to 5000 kPa is applicable.
    In a particular embodiment of any of the above embodiments 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 feedstock is introduced into the first ketonisation reactor together with a first carrier gas stream comprising CO2; and • the gas comprising CO2 is separated from the effluent exiting the first ketonisation reactor whereby the effluent is introduced into the second ketonisation reactor together with a second carrier gas stream comprising CO2; and • if the system comprises more than two ketonisation reactors, 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;
    • gas comprising CO2 is separated from the effluent exiting the final ketonisation reactor whereby the effluent comprising ketones is used for recovery; and • the separated gas streams comprising CO2 are recycled and used as the carrier gas stream in one or more of the ketonisation reactor(s).
    In this embodiment, wherein the ketonisation reactors are arranged in series, 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.
    In this embodiment, wherein the ketonisation reactors are arranged in series, 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.
    This measurement helps to control the adiabatic temperature decrease in ketonisation and makes operation more cost efficient. 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.
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    In any of the above embodiments 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.
    In any of the above embodiments 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.
    In any of the above embodiments 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.
    In any of the above embodiments substantially pure CO2 may be recovered and subjected to compression, optionally under heating, before recycling it to a ketonisation reactor.
    In any of the above embodiments the heat generated by the cooling may be used for compression under heating of the substantially pure CO2.
    In any of the above embodiments 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 and isomerisation
    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 CoMo, 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/oil 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
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    20176135 prh 19-12-2017 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.
    Hydrofinishing
    In the hydrofinishing step, if applied, 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/oil ratio may for example be 100-500 nl/l.
    The second aspect of the invention
    In a first embodiment of this aspect of the invention it 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.
    In a second embodiment the system according to the present invention may comprise two, three or four ketonisation reactors, preferably in series.
    In any of these embodiments 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 • recycling means for liquid comprising unreacted fatty acids and/or fatty avid derivatives (11) and outlet means for separated CO2 (12).
    In any of these embodiments one or more ketonisation reactor(s) is a trickle bed reactor.
    In any of these embodiments the system may further comprise means for purification of gas comprising CO2, such as means for separation CO2 and/ H2O vapour from volatile organic compounds.
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    The third aspect of the invention
    In a first embodiment of this aspect the use of a gas comprising CO2 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. By enhancing is meant that a more uniform gas flow pattern is allowed throughout the reaction zone. As the reactor has both CO2 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.
    In a second embodiment of this aspect, and before recycling, the separated gas comprising CO2 has been purified and recovered in a separation process comprising steps of separating CO2 from H2O vapour and/or volatile organic compounds and optionally separated as substantially pure CO2 from the waste water. Part of CO2 may be retrieved as a product before recycling. This CO2 is quite pure.
    In any of the above embodiments separated gas comprising CO2 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.
    In any of the above embodiments substantially pure CO2 has been recovered and subjected to compression, optionally under heating, before recycled to a ketonisation reactor.
    The fourth aspect of the invention
    In its 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 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 end products 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.
    Table 1API base stock categoriesGroupSulphur, wt.-% Saturates, %Viscosity Index (VI)1>0.03and/or<9080-119II<0.03And>9080-119
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    III<0.03And>90> 120IVSynthetic poly-alpha-olefins (PAOs)VAny other type of base oil than group l-IV
    20176135 prh 19-12-2017
    Exemplary embodiments of the invention are now described with reference to the drawings. Figures 1 and 2 depict the equipment and streams indicated in the lists preceding the embodiments.
    Figure 1
    Equipment:
    A Reactor
    B Reactor
    C Reactor
    D Gas-liquid separator
    E Gas-liquid separator
    F Compressor
    Streams:
    Fatty acid feedstock to Reactor A
    Liquid from Reactor A
    Liquid from Reactor B
    4 Liquid from Reactor C
    CO2 to Reactor A
    CO2 to Reactor B
    CO2 to Reactor C
    Gas from Reactor A
    9 Gas from Reactor B
    Gas from Reactor C
    Liquid from Gas-liquid separator D
    Product CO2
    Ketonisation catalyst bed
    A fatty acid feedstock (1), which may partly be in liquid form, and comprising fatty acids and/or fatty acid derivatives having an average chain length of Cn (n = 4 or more) is processed in a ketonisation system wherein the ketonisation reaction is conducted in a catalyst bed system comprising three reactors (A, B, C) in series. The ketonisation catalyst beds (G) include a suitable 30 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, and 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
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    20176135 prh 19-12-2017 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 C2n-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 10 CO2. CO2 is separated from the effluent (2), is recovered and lead as a gas stream (8) to a first gasliquid 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 15 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).
    Finally, the effluent (4) leaving reactor C comprising ketones produced by the ketonisation reaction and CO2 is obtained. CO2 is separated from effluent 4 as described for effluent 2, is 20 recovered and lead as a gas stream (10) to the gas-liquid separator D. Separation of the gas stream 10 from the effluent 4 leaves the target ketones for recover and further treatment.
    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 25 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). Thereafter 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 CO2.
    Figure 2
    Equipment:
    A Reactor
    B Reactor
    C Gas-liquid separator
    D Gas-liquid separator
    E Compressor
    F Catalyst bed
    Streams:
    Fatty acid feedstock to Reactor A
    Liquid from Reactor A
    Liquid from Reactor B
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    20176135 prh 19-12-2017
    CO2 to Reactor A
    CO2 to Reactor B
    Gas from Reactor A
    Gas from Reactor B
    8 Liquid from Gas-liquid separator C
    Product CO2
    A fatty acid feedstock (1), which may partly be in liquid form, and comprising fatty acids and/or fatty acid derivatives having an average chain length of Cn (n=4 or more) is processed in a 10 ketonisation system wherein the ketonisation reaction is conducted in a catalyst bed system comprising two reactors (A, B) in series. The ketonisation catalyst beds (G) include a suitable ketonisation catalyst. The first reactor (A) is loaded with a certain amount of catalyst, and 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 C2n_i.
    The fatty acid 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 (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 (6) to a first gas-liquid separator (C).
    The remaining part of effluent 2, free of CO2, is lead to reactor B, and at the same time a flow (5) 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 (7) to gas-liquid separator C. Separation of the gas stream (7) from effluent 3 leaves the target ketones for recover and further treatment.
    Each gas stream (6, 7) recovered from the reactor effluents (2, 3) are subjected to cooling and lead to the gas-liquid separator C. The separation in gas-liquid separator C leaves a gas flow comprising CO2and H2O which is lead to a second separator (D). CO2 is recovered in separator D and purified to a substantially pure CO2 stream (9). Thereafter the CO2 stream 9 is compressed in 40 the compressor (E) before it is used as carrier gas stream to be used in one of the reactors (A, B).
    Heat released by cooling of the gas streams (6, 7) is partly utilised for re-heating of compressed CO2.
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    Examples
    Example 1 (Figure 1)
    Pure Cig 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/TiO2 catalyst; loaded as 13,000 kg in the first reactor, 14,000 kg in 5 the second reactor, and 22,000 kg in the third reactor.
    The target product of the ketonisation of Ci6 acids is C3i-ketones.
    The feed temperature was 350 °C in all reactors (A, B, C). The inlet pressure in the three reactors 10 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 20 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). In 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 25 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 30 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 35 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. For the further cooling between the two separators (D, E), a water cooler operating at 40 °C was used.
    Example 2:
    Yield and mass flow
    The ketonisation reaction provided C3i in a high yield and with high selectivity. Results are shown 40 in Table 2.
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    Table 2: Yield and mass flowLiquid product Molar conversion of feedstock fatty acids99%Molar selectivity to C31 ketone93%Weight based yield of C31 ketone from palmitic acid (theor. 87.9%)82% (93% out of theoretical yield)Weight based yield of base oil precursors (C31 ketone, other ketones, heavies)85%Weight based yield of diesel precursors from palmitic acid2%Mass fraction of heavies in base oil precursors3.8%Total mass flow of base oil precursors kg/h17,040 CO2 product, split from the recycling Mass flow kg/h (12)1,710Purity of CO2 99.99% Organic side stream from the second separator (E) Mass flow kg/h190Weight fraction of diesel precursors92% Waste water from the second separator (E) Mass flow kg/h690Purity of water100%
    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 5 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 10 CO2 flow rate is 15,000 kg/h.
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    Energy consumption:
    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.
    20176135 prh 19-12-2017
    Table 3 Heat exchangers Fatty acid feed heater (to heat the feedstock from 100 °C to 350 °C)4257 kWHeater for liquid product from Reactor A130 kWHeater for liquid product from Reactor B522 kWExchanger for reactor gas phase effluent (5, 6, 7)-686 kWExchanger for heating of recycled CO2 (12)686 kWAir cooler for additional cooling of reactor gas stream (5, 6, 7)-692 kWElectric heater for additional heating of recycledCO2 stream838 kWWater cooler for gas effluent of gas-liquid separator (D, E)-1222 kW Pumps Liquid product pump (discharge pressure 4500 kPa for HDO)25.3 kWPump for returning un-reacted feedstock to Reactor C(11)1.3 kW Compressor For re-pressurizing CO2 (F)154 kW
    Example 3:
    Table 4 shows the ranges of other key ketonisation parameters
    Table 4 Process variableMin.Max.CO2 flow (kg/h)as low as still effective15,000Temperature (°C)330360Pressure (kPa)10002500WHSV (1/h)0.2as high as possible
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    Example 4:
    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 5 leading to a high, viz. >83 wt.-% out of theoretical 87.9 wt.-%, base oil precursor yield is indicated.
    Table 5 ^feedstockLoading of reactor ALoading of reactor BLoading of reactor CEffective WHSV (1/h)340 °C20,000 kg22,000 kg33,000 kg0.27345 °C16,000 kg17,000 kg25,000 kg0.34350 °C13,000 kg14,000 kg22,000 kg0.41355 °C11,000 kg12,000 kg18,000 kg0.49360 °C8,000 kg9,000 kg15,000 kg0.63
    If the system works at 340 °C or below, it may be advantageous to use four reactors instead of three.
    Example 5 (Figure 2)
    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.
    权利要求:
    Claims (30)
    [1] Claims
    1. 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 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 • the feedstock is introduced into a ketonisation reactor together with a carrier gas stream comprising CO2;
    • 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; and • the separated gas comprising CO2 is recycled and used as the carrier gas stream of a ketonisation reactor.
    [2] 2. Method according to claim 1, wherein the feedstock is at least partly in liquid phase, such as 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.
    [3] 3. Method according to any one of the claims 1 to 2, wherein the feedstock of biological origin comprises saturated free fatty acids and/or saturated fatty acid esters, such as esters, amides, aldehydes, alcohols, anhydrides, metal salts, or mixture thereof, preferably fatty acid glycerols.
    [4] 4. Method according to any one of the claims 1 to 3, wherein the feedstock of biological origin comprises saturated free fatty acids and/or saturated fatty acid esters having an average carbon chain length of from C4 to C24, preferably having an average carbon chain length of from C6 to C24.
    [5] 5. Method according to any one of the claims 1 to 4, wherein the catalyst bed comprises a ketonisation catalyst which is a metal oxide catalyst, preferably 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.
    [6] 6. Method according to any of the claims 1 to 5, wherein the temperature in the feedstock is at least 330 °C, preferably at least 340 °C, more preferably at least 350 °C, even more preferably at least 355 °C, and most preferred 360-365°C.
    [7] 7. Method according to any one of the claims 1 to 6, wherein the pressure in a ketonisation reactor is as 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.
    [8] 8. Method according to any one of the claims 1 to 7, wherein the liquid feed flow rate, WHSV, is from 0.1 to 10 IT1, preferably from 0.2 to 5 h1, more preferably from 0.3 to 3 h1, most preferably from 0.5 to 1 h1.
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    20176135 prh 19-12-2017
    [9] 9. A method according to any one of the claims 1 to 8, wherein 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 feedstock is introduced into the first ketonisation reactor together with a first carrier gas stream comprising CO2; and • the gas comprising CO2 is separated from the effluent exiting the first ketonisation reactor whereby the effluent is introduced into the second ketonisation reactor together with a second carrier gas stream comprising CO2; and • if the system comprises more than two ketonisation reactors, 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;
    • gas comprising CO2 is separated from the effluent exiting the final ketonisation reactor whereby the effluent comprising ketones is used for recovery; and • the separated gas streams comprising CO2 are recycled and used as the carrier gas stream in one or more of the ketonisation reactor(s).
    [10] 10. Method according to claim 9, wherein the pressure in each ketonisation reactor in series following the first ketonisation reactor is lower than the pressure in the preceding ketonisation reactor.
    [11] 11. Method according to any of the claims 9 and 10, wherein the catalyst loading in the catalyst bed in each ketonisation reactor in series following the first ketonisation reactor is higher than the catalyst loading in the first ketonisation reactor, preferably at least 10 % higher in the second reactor, and/or preferably at least 50 % higher in the third reactor.
    [12] 12. Method according to any of the claims 1 to 11, wherein the system comprises at least two ketonisation reactors.
    [13] 13. Method according to claim 12, wherein the effluent exiting a ketonisation reactor and separated from gas comprising CO2 is heated before introduction into a subsequent ketonisation reactor.
    [14] 14. Method according to any of the claims 1 to 13, wherein the separated gas streams comprising CO2 are purified before recycling, and recovered in a separation process comprising steps of separating CO2 and H2O vapour from unreacted fatty acids 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 wherein the unreacted fatty acids and/or fatty acid derivatives are optionally recycled to a ketonisation reactor.
    [15] 15. Method according to claim 14, wherein the separated gas comprising CO2 is subject to purification, such as by cooling, and optionally further purification, and/or wherein the recovered purified gas is dried before recycling to a ketonisation reactor.
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    20176135 prh 19-12-2017
    [16] 16. Method according to any of the claims 14 to 15, wherein substantially pure CO2 is recovered and subjected to compression, optionally under heating, before recycled to a ketonisation reactor.
    [17] 17. Method according to any of the claims 15 to 16, wherein the heat generated by the cooling is used for compression under heating of the substantially pure CO2.
    [18] 18. Method according to any of the claims 1 to 17, which method further comprises a hydrodeoxygenation step, an optional isomerisation step and optional hydrofinishing steps.
    [19] 19. 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 catalyst bed (F), means for heating, preferably an oil heater, inlet means for the feedstock (1) and outlet means for the effluent (2, 3) exiting a ketonisation reactor, wherein • the one or more ketonisation reactors each further comprises inlet means for carrier gas streams (4, 5), outlet means for separated gas streams comprising CO2 (6, 7); and wherein • the system further comprises one or more gas-liquid separators (C, D) for separating CO2 in the separated gas streams (6, 7) from H2O vapour, unreacted fatty acids and/or fatty acid derivatives, and/or volatile organic compounds, and means (E) for recirculating and optionally compressing the separated CO2; and optionally • recycling means for liquid comprising unreacted fatty acids and/or fatty acid derivatives (8) and outlet means for separated CO2 (9).
    [20] 20. System according to claim 19, further comprising 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.
    [21] 21. System according to any one of the claims 19 to 20 comprising two, three or four ketonisation reactors, preferably in series.
    [22] 22. System according to any one of the claims 19 to 21 wherein • the system comprises three ketonisation reactors (A, B, C), preferably in series, each comprising a ketonisation catalyst bed (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
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    20176135 prh 19-12-2017 fatty acid derivatives, and/or volatile organic compounds, and means (F) for recirculating and optionally compressing the separated CO2; and optionally • recycling means for liquid comprising unreacted fatty acids and/or fatty avid derivatives (11) and outlet means for separated CO2 (12).
    [23] 23. System according to any one of the claims 19 to 22, wherein the one or more ketonisation reactors is a trickle bed reactor.
    [24] 24. System according to any one of the claims 19 to 23, further comprising means for purification of gas comprising CO2, such as means for separating CO2 and/ H2O vapour from volatile organic compounds.
    [25] 25. Use of a gas comprising CO2 as a carrier gas stream in a ketonisation reaction, wherein the gas comprising CO2has 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.
    [26] 26. Use according to claim 25 for 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.
    [27] 27. Use according to any one of claims 25 and 26, wherein the separated gas comprising CO2 before recycling has been purified and recovered in a separation process comprising steps of separating CO2 from H2O vapour and/or volatile organic compounds and optionally separated as substantially pure CO2 from the waste water.
    [28] 28. Use according to claim 27, wherein the separated gas comprising CO2 has been subject to cooling before purification, and/or wherein the recovered purified gas has been dried before recycling to a ketonisation reactor.
    [29] 29. Use according to any one of the claims 25 to 29, wherein substantially pure CO2 has been recovered and subjected to compression, optionally under heating, before recycled to a ketonisation reactor.
    [30] 30. Use of ketones obtainable by a method of any of the claims 1 to 18 for the manufacture of base oil or base oil components.
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    同族专利:
    公开号 | 公开日
    PT3502211T|2020-09-17|
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    FI128062B|2019-08-30|
    EP3502211A1|2019-06-26|
    JP2021506754A|2021-02-22|
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    KR20200100045A|2020-08-25|
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    SG11202003092RA|2020-07-29|
    ES2818975T3|2021-04-14|
    US10968398B2|2021-04-06|
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