WO2002064710A2 - Base oil composition - Google Patents
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- WO2002064710A2 WO2002064710A2 PCT/EP2002/001634 EP0201634W WO02064710A2 WO 2002064710 A2 WO2002064710 A2 WO 2002064710A2 EP 0201634 W EP0201634 W EP 0201634W WO 02064710 A2 WO02064710 A2 WO 02064710A2
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- WIPO (PCT)
- Prior art keywords
- base oil
- paraffins
- fraction
- cyclo
- formulation
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- 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
- C10M171/00—Lubricating compositions characterised by purely physical criteria, e.g. containing as base-material, thickener or additive, ingredients which are characterised exclusively by their numerically specified physical properties, i.e. containing ingredients which are physically well-defined but for which the chemical nature is either unspecified or only very vaguely indicated
- C10M171/02—Specified values of viscosity or viscosity index
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2/00—Production of liquid hydrocarbon mixtures of undefined composition from oxides of carbon
- C10G2/30—Production of liquid hydrocarbon mixtures of undefined composition from oxides of carbon from carbon monoxide with hydrogen
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2/00—Production of liquid hydrocarbon mixtures of undefined composition from oxides of carbon
- C10G2/30—Production of liquid hydrocarbon mixtures of undefined composition from oxides of carbon from carbon monoxide with hydrogen
- C10G2/32—Production of liquid hydrocarbon mixtures of undefined composition from oxides of carbon from carbon monoxide with hydrogen with the use of catalysts
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G45/00—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds
- C10G45/58—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds to change the structural skeleton of some of the hydrocarbon content without cracking the other hydrocarbons present, e.g. lowering pour point; Selective hydrocracking of normal paraffins
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- 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
- C10M101/00—Lubricating compositions characterised by the base-material being a mineral or fatty oil
- C10M101/02—Petroleum fractions
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- 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
- C10M107/00—Lubricating compositions characterised by the base-material being a macromolecular compound
- C10M107/02—Hydrocarbon polymers; Hydrocarbon polymers modified by oxidation
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- 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
- C10M169/00—Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
- C10M169/04—Mixtures of base-materials and additives
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2400/00—Products obtained by processes covered by groups C10G9/00 - C10G69/14
- C10G2400/04—Diesel oil
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2400/00—Products obtained by processes covered by groups C10G9/00 - C10G69/14
- C10G2400/06—Gasoil
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2400/00—Products obtained by processes covered by groups C10G9/00 - C10G69/14
- C10G2400/08—Jet fuel
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2400/00—Products obtained by processes covered by groups C10G9/00 - C10G69/14
- C10G2400/10—Lubricating oil
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- 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
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/17—Fisher Tropsch reaction products
- C10M2205/173—Fisher Tropsch reaction products used as base material
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/02—Pour-point; Viscosity index
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/04—Detergent property or dispersant property
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/12—Inhibition of corrosion, e.g. anti-rust agents or anti-corrosives
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
- C10N2040/252—Diesel engines
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- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S208/00—Mineral oils: processes and products
- Y10S208/95—Processing of "fischer-tropsch" crude
Definitions
- the invention is directed to a lubricating base oil composition
- a lubricating base oil composition comprising at least 95 wt% saturates, of which saturates fraction between 10 and 40 wt% are cyclo- paraffins and the remainder being n- and iso-paraffins, said composition having a viscosity index of above 120 and a pour point of below -15 °C.
- WO-A-0014179 Known from WO-A-0014179, WO-A-0014183, WO-A-0014187 and WO-A-0014188 are lubricant base stock comprising at least 95 wt% of non-cyclic isoparaffins .
- WO-A-0118156 describes a base oil derived from a Fischer-Tropsch product having a naphthenics content of less than 10%.
- the base oils as disclosed in applicant's patent applications EP-A-776959 or EP-A-668342 have been found to comprise less than 10 wt% of cyclo-paraffins.
- Example 2 and 3 of EP-A-776959 and base oils were obtained, from a waxy Fischer-Tropsch synthesis product, wherein the base oils consisted of respectively about 96 wt% and 93 wt% of iso- and normal paraffins.
- Applicants further prepared a base oil having a pour point of -21 °C by catalytic dewaxing a Shell MDS Waxy Raffinate (as obtainable from Shell MDS Malaysia Sdn Bhd) using a catalyst comprising synthetic ferrierite and platinum according to the teaching of EP-A-668342 and found that the content of iso- and normal paraffins was about 94 wt%.
- a lubricating base oil composition having an improved solvency when compared to the disclosed base oils. This is found to be advantageous in for example industrial formulations such as turbine oils and hydraulic oils comprising for the greater part the base oil according to the invention. Furthermore the base oil compositions will cause seals in for example motor engines to swell more than the prior art base oils. This is advantageous because due to said swelling less lubricant loss will be observed in certain applications. Applicants have found that such a base oil is an excellent API Group III base oil having improved solvency properties.
- the lubricating base oil composition comprises preferably at least 98 wt% saturates, more preferably at least 99.5 wt% saturates and most preferably at least 99.9 wt%.
- This saturates fraction in the base oil comprises between 10 and 40 wt% of cyclo-paraffins.
- the content of cyclo-paraffins is less than 30 wt% and more preferably less than 20 wt%.
- the content of cyclo-paraffins is at least 12 wt% and more preferably at least 15 wt%.
- the unique and novel base oils are further characterized in that the weight ratio of 1-ring cyclo-paraffins relative to cyclo- paraffins having two or more rings is greater than 3 preferably greater than 5. It was found that this ratio is suitably smaller than 15.
- the cyclo-paraffin content as described above is measured by the following method. Any other method resulting in the same results may also be used.
- the base oil sample is first separated into a polar (aromatic) phase and a non-polar (saturates) phase by making use of a high performance liquid chromatography (HPLC) method IP368/01, wherein as mobile phase pentane is used instead of hexane as the method states.
- HPLC high performance liquid chromatography
- the saturates and aromatic fractions are then analyzed using a Finnigan MAT90 mass spectrometer equipped with a Field desorption/Field lonisation (FD/FI) interface, wherein FI (a "soft” ionisation technique) is used for the semi- quantitative determination of hydrocarbon types in terms of carbon number and hydrogen deficiency.
- FI Field desorption/Field lonisation
- the type classification of compounds in mass spectrometry is determined by the characteristic ions formed and is normally classified by " z number".
- the base oil composition preferably has a content of aromatic hydrocarbon compounds of less than 1 wt%, more preferably less than 0.5 wt% and most preferably less than 0.1 wt%, a sulphur content of less than 20 ppm and a nitrogen content of less than 20 ppm.
- the pour point of the base oil is preferably less than -30 °C and more preferably lower than -40 °C.
- the viscosity index is higher than 120. It has been found that the novel base oils typically have a viscosity index of below 140.
- the kinematic viscosity at 100 °C of the base oil is preferably between 3.5 and 6 cSt and the Noack volatility is between 6 and 14 wt%. Applicants found that the base oil according to the invention is suitably prepared according to the following process wherein the following steps are performed:
- step (b) hydrocracking/hydroisomerisating the Fischer-Tropsch product, (c) separating the product of step (b) into one or more gas oil fractions, a base oil precursor fraction and a higher boiling fraction,
- step (d) performing a pour point reducing step to the base oil precursor fraction obtained in step (c) , and (e) recovering the lubricating base oil from the effluent of step (d) .
- Step (a) is preferably performed by making use of a specific catalyst in order to obtain the relatively heavy Fischer-Tropsch product.
- the Fischer-Tropsch catalyst is suitably a cobalt-containing catalyst as obtainable by (aa) mixing (1) titania or a titania precursor, (2) a liquid, and (3) a cobalt compound, which is at least partially insoluble in the amount of liquid used, to form a mixture; (bb) shaping and drying of the mixture thus obtained; and (cc) calcination of the composition thus obtained.
- the cobalt compound is insoluble in the amount of liquid used, more preferably at least 70 weight percent, and even more preferably at least 80 weight percent, and most preferably at least 90 weight percent.
- the cobalt compound is metallic cobalt powder, cobalt hydroxide or an cobalt oxide, more preferably Co (OH) 2 or C03O4.
- the cobalt compound is used in an amount of up to 60 weight percent of the amount of refractory oxide, more preferably between 10 and 40 wt percent.
- the catalyst comprises at least one promoter metal, preferably manganese, vanadium, rhenium, ruthenium, zirconium, titanium or chromium, most preferably manganese.
- the promoter metal (s) is preferably used in such an amount that the atomic ratio of cobalt and promoter metal is at least 4, more preferably at least 5.
- at least one promoter metal compound is present in step (aa) .
- the cobalt compound is obtained by precipitation, optionally followed by calcination.
- the cobalt compound and at least one of the compounds of promoter metal are obtained by co-precipitation, more preferably by co-precipitation at constant pH.
- the cobalt compound is precipitated in the presence of at least a part of the titania or the titania precursor, preferably in the presence of all titania or titania precursor.
- the mixing in step (aa) is performed by kneading or mulling.
- the thus obtained mixture is subsequently shaped by pelletising, extrusion, granulating or crushing, preferably by extrusion.
- the mixture obtained has a solids content in the range of from 30 to 90% by weight, preferably of from 50 to 80% by weight.
- the mixture formed in step (aa) is a slurry and the slurry thus-obtained is shaped and dried by spray-drying.
- the slurry obtained has a solids content in the range of from 1 to 30% by weight, more preferably of from 5 to 20% by weight.
- the calcination is carried out at a temperature between 400 and 750 °C, more preferably between 500 and 650 °C. Further details are described in WO-A-9934917.
- the process is typically carried out at a temperature in the range from 125 to 350 °C, preferably 175 to 275 °C.
- the pressure is typically in the range from 5 to 150 bar abs., preferably from 5 to 80 bar abs., in particular from 5 to 50 bar abs.
- Hydrogen (H2) and carbon monoxide (synthesis gas) is typically fed to the process at a molar ratio in the range from 0.5 to 2.5.
- the gas hourly space velocity (GHSV) of the synthesis gas in the process of the present invention may vary within wide ranges and is typically in the range from 400 to 10000 Nl/l/h, for example from 400 to 4000 Nl/l/h.
- GHSV is well known in the art, and relates to the volume of synthesis gas in Nl, i.e. litres at STP conditions (0 °C and 1 bar abs), which is contacted in one hour with one litre of catalyst particles, i.e. excluding interparticular void spaces . In the case of a fixed catalyst bed, the GHSV may also be expressed as per litre of catalyst bed, i.e. including interparticular void space. Step (a) can be performed in a slurry reactor or preferably in a fixed bed. Further details are described in WO-A-9934917.
- the Fischer-Tropsch product obtained in step (a) is used in step (b) .
- This product has at least 30 wt%, preferably at least 50 wt% and more preferably at least 55 wt%, of compounds having at least 30 carbon atoms.
- the weight ratio of compounds having at least 60 or more carbon atoms and compounds having at least 30 carbon atoms of the Fischer- Tropsch product is at least 0.2, preferably at least 0.4 and more preferably at least 0.55.
- the Fischer-Tropsch product comprises a C20 + fraction having an ASF-alpha value (Anderson-Schulz-Flory chain growth factor) of at least 0.925, preferably at least 0.935, more preferably at least 0.945, even more preferably at least 0.955.
- the initial boiling point of the Fischer- Tropsch product may range up to 400 °C, but is preferably below 200 °C.
- the Fischer-Tropsch product as described in detail above suitably has a content of non-branched compounds of above 80 wt%.
- other fractions may be additionally processed in step (b) .
- a possible other fraction may suitably be the higher boiling fraction obtained in step (c) or part of said fraction.
- the Fischer-Tropsch product will contain no or very little sulphur and nitrogen containing compounds. This is typical for a product derived from a Fischer-Tropsch reaction, which uses synthesis gas containing almost no impurities. Sulphur and nitrogen levels will generally be below the detection limit, which is currently 1 ppm for nitrogen and 5 ppm for sulphur.
- the Fischer-Tropsch product can optionally be subjected to a mild hydrotreatment step before performing step (b) in order to remove any oxygenates and saturate any olefinic compounds present in the reaction product of the Fischer-Tropsch reaction.
- a mild hydrotreatment is described in EP-B-668342.
- the hydrocracking/hydroisomerisation reaction of step (b) is preferably performed in the presence of hydrogen and a catalyst, which catalyst can be chosen from those known to one skilled in the art as being suitable for this reaction.
- Catalysts for use in step (b) typically comprise an acidic functionality and a hydrogenation/dehydrogenation functionality.
- Preferred acidic functionalities are refractory metal oxide carriers.
- Suitable carrier materials include silica, alumina, silica-alumina, zirconia, titania and mixtures thereof.
- Preferred carrier materials for inclusion in the catalyst for use in the process of this invention are silica, alumina and silica-alumina.
- a particularly preferred catalyst comprises platinum or platinum/ palladium supported on a silica-alumina carrier.
- a halogen moiety in particular fluorine, or a phosphorous moiety to the carrier, may enhance the acidity of the catalyst carrier.
- suitable hydrocracking/hydroisomerisation processes and suitable catalysts are described in WO-A-0014179, EP-A-532118, EP-B-666894 and the earlier referred to EP-A-776959.
- the hydrocracking catalyst may also contain a molecular sieve as for example described in US-A-5362378.
- Preferred hydrogenation/dehydrogenation functionalities are Group VIII noble metals, for example palladium and more preferably platinum or platinum/ palladium alloys.
- the catalyst may comprise the hydrogenation/dehydrogenation active component in an amount of from 0.005 to 5 parts by weight, preferably from 0.02 to 2 parts by weight, per 100 parts by weight of carrier material.
- a particularly preferred catalyst for use in the hydroconversion stage comprises platinum in an amount in the range of from 0.05 to 2 parts by weight, more preferably from 0.1 to 1 parts by weight, per 100 parts by weight of carrier material.
- the catalyst may also comprise a binder to enhance the strength of the catalyst.
- the binder can be non-acidic. Examples are clays and other binders known to one skilled in the art.
- step (b) the feed is contacted with hydrogen in the presence of the catalyst at elevated temperature and pressure.
- the temperatures typically will be in the range of from 175 to 380 °C, preferably higher than 250 °C and more preferably from 300 to 370 °C.
- the pressure will typically be in the range of from 10 to 250 bar and preferably between 20 and 80 bar.
- Hydrogen may be supplied at a gas hourly space velocity of from 100 to 10000 Nl/l/hr, preferably from 500 to 5000 Nl/l/hr.
- the hydrocarbon feed may be provided at a weight hourly space velocity of from 0.1 to 5 kg/l/hr, preferably higher than 0.5 kg/l/hr and more preferably lower than 2 kg/l/hr.
- the ratio of hydrogen to hydrocarbon feed may range from 100 to 5000 Nl/kg and is preferably from 250 to 2500 Nl/kg.
- the conversion in step (b) as defined as the weight percentage of the feed boiling above 370 °C which reacts per pass to a fraction boiling below 370 °C, is at least 20 wt%, preferably at least 25 wt%, but preferably not more than 80 wt%, more preferably not more than 65 wt%.
- the feed as used above in the definition is the total hydrocarbon feed fed to step (b) , thus also any optional recycles, such as the higher boiling fraction as obtained in step (c) .
- step (c) the product of step (b) is separated into one or more gas oil fractions, a base oil precursor fraction having preferably a T10wt% boiling point of between 200 and 450 °C and a T90wt% boiling point of between 300 and 650 preferably 550 °C and a higher boiling fraction.
- a haze free base oil grade can be obtained having also excellent other quality properties.
- the separation is preferably performed by means of a first distillation at about atmospheric conditions, preferably at a pressure of between 1.2-2 bara, wherein the gas oil product and lower boiling fractions, such as naphtha and kerosine fractions, are separated from the higher boiling fraction of the product of step (b) .
- the higher boiling fraction of which suitably at least 95 wt% boils above 350 preferably above 370 °C, is subsequently further separated in a vacuum distillation step wherein a vacuum gas oil fraction, the base oil precursor fraction and the higher boiling fraction are obtained.
- the vacuum distillation is suitably performed at a pressure of between 0.001 and 0.05 bara.
- step (d) the base oil precursor fraction obtained in step (c) is subjected to a pour point reducing treatment.
- a pour point reducing treatment is understood every process wherein the pour point of the base oil is reduced by more than 10 °C, preferably more than 20 °C, more preferably more than 25 °C.
- step (d) is performed by means of a catalytic dewaxing process.
- a catalytic dewaxing process it has been found that base oils having a pour point of below -20 °C and even below -40 °C can be prepared when starting from a base oil precursor fraction as obtained in step (c) .
- the catalytic dewaxing process can be performed by any process wherein in the presence of a catalyst and hydrogen the pour point of the base oil precursor fraction is reduced as specified above.
- Suitable dewaxing catalysts are heterogeneous catalysts comprising a molecular sieve and optionally in combination with a metal having a hydrogenation function, such as the
- Group VIII metals Molecular sieves, and more suitably intermediate pore size zeolites, have shown a good catalytic ability to reduce the pour point of the base oil precursor fraction under catalytic dewaxing conditions.
- the intermediate pore size zeolites have a pore diameter of between 0.35 and 0.8 nm.
- Suitable intermediate pore size zeolites are mordenite, ZSM-5, ZSM-12, ZSM-22, ZSM-23, SSZ-32, ZSM-35 and ZSM-48.
- Another preferred group of molecular sieves are the silica-aluminaphosphate (SAPO) materials of which SAPO-11 is most preferred as for example described in US-A-4859311.
- SAPO silica-aluminaphosphate
- ZSM-5 may optionally be used in its HZSM-5 form in the absence of any Group VIII metal.
- the other molecular sieves are preferably used in combination with an added Group VIII metal.
- Suitable Group VIII metals are nickel, cobalt, platinum and palladium. Examples of possible combinations are Ni/ZSM-5, Pt/ZSM-23, Pd/ZSM-23, Pt/ZSM-48 and Pt/SAPO-11. Further details and examples of suitable molecular sieves and dewaxing conditions are for example described in WO-A-9718278, US-A-5053373, US-A-5252527 and US-A-4574043.
- the dewaxing catalyst suitably also comprises a binder.
- the binder can be a synthetic or naturally occurring (inorganic) substance, for example clay, silica and/or metal oxides. Natural occurring clays are for example of the montmorillonite and kaolin families.
- the binder is preferably a porous binder material, for example a refractory oxide of which examples are: alumina, silica-alumina, silica-magnesia, silica- zirconia, silica-thoria, silica-beryllia, silica-titania as well as ternary compositions for example silica- alumina-thoria, silica-alumina-zirconia, silica-alumina- magnesia and silica-magnesia-zirconia . More preferably a low acidity refractory oxide binder material, which is essentially free of alumina, is used.
- binder materials are silica, zirconia, titanium dioxide, germanium dioxide, boria and mixtures of two or more of these of which examples are listed above.
- the most preferred binder is silica.
- a preferred class of dewaxing catalysts comprise intermediate zeolite crystallites as described above and a low acidity refractory oxide binder material which is essentially free of alumina as described above, wherein the surface of the aluminosilicate zeolite crystallites has been modified by subjecting the aluminosilicate zeolite crystallites to a surface dealumination treatment.
- a preferred dealumination treatment is by contacting an extrudate of the binder and the zeolite with an aqueous solution of a fluorosilicate salt as described in for example US-A-5157191.
- suitable dewaxing catalysts as described above are silica bound and dealuminated Pt/ZSM-5, silica bound and dealuminated Pt/ZSM-23, silica bound and dealuminated Pt/ZSM-12, silica bound and dealuminated Pt/ZSM-22, as for example described in WO-A-0029511 and EP-B-832171.
- Catalytic dewaxing conditions typically involve operating temperatures in the range of from 200 to 500 °C, suitably from 250 to 400 °C, hydrogen pressures in the range of from 10 to 200 bar, preferably from 40 to 70 bar, weight hourly space velocities (WHSV) in the range of from 0.1 to 10 kg of oil per litre of catalyst per hour (kg/l/hr), suitably from 0.2 to 5 kg/l/hr, more suitably from 0.5 to 3 kg/l/hr and hydrogen to oil ratios in the range of from 100 to 2,000 litres of hydrogen per litre of oil.
- WHSV weight hourly space velocities
- the base oils according to the invention can be suitably used as part of a motor engine lubricant composition comprising also at least one lubricant additive. Because of its improved solvency as compared to poly-alpha olefins or to the base oils having the lower cyclo-paraffin content as disclosed in the above cited publications it has been found possible to advantageously formulate said lubricants without having to add substantial volumes of (di-) esters which are typically used to increase the solvency of said base oils. Preferably the content of such additional base oil is less than 10 wt% in said formulation.
- the lubricant composition comprises the base oil and one or more additives wherein the lubricant composition has a kinematic viscosity at 100 °C of more than 5.6 cSt, a cold cranking simulated dynamic viscosity at -35 °C according to ASTM D 5293 of less than 62 centiPoise (cP) and a mini rotary viscosity test value of less than 60000 cP according to ASTM D 4684.
- SAE OW-x compositions Such lubricant compositions are also referred to as SAE OW-x compositions.
- SAE stands for Society of Automotive Engineers in the USA.
- the "0" number in such a designation is associated with a maximum viscosity requirement at -35 °C for that composition as measured typically by a cold cranking simulator (VdCCS) under high shear.
- the second number "x” is associated with a kinematic viscosity requirement at 100 °C.
- the base oil as obtainable by the above processes has a pour point of less than -39 °C and a kinematic viscosity at 100 °C which is suitably between 4 and 8 cSt .
- the actual kinematic viscosity at 100 °C will depend on the specific OW-x grade one wishes to prepare.
- a base oil having a kinematic viscosity at 100 °C of between 3.8 and 5.5 cSt is suitably used.
- a base oil having a kinematic viscosity at 100 °C of between 5.5 and 8 cSt is suitably used.
- Such a lubricant formulation is preferably used as an OW-x passenger car motor oil or OW-x heavy duty diesel engine oil, wherein x is 20, 30 or 40.
- the OW-x lubricant composition comprises one or more additives.
- additive types which may form part of the composition are dispersants, detergents, viscosity modifying polymers, extreme pressure/antiwear additives, antioxidants, pour point depressants, emulsifiers, demulsifiers, corrosion inhibitors, rust inhibitors, antistaining additives, friction modifiers. Specific examples of such additives are described in for example Kirk-Othmer Encyclopedia of Chemical Technology, third edition, volume 14, pages 477-526.
- the anti-wear additive is a zinc dialkyl dithiophosphate.
- the dispersant is an ashless dispersant, for example polybutylene succinimide polyamines or Mannic base type dispersants.
- the detergent is an over-based metallic detergent, for example the phosphonate, sulfonate, phenolate or salicylate types as described in the above referred to
- the antioxidant is a hindered phenolic or aminic compound, for example alkylated or styrenated diphenylamines or ionol derived hindered phenols.
- the viscosity modifier is a viscosity modifying polymer, for example polyisobutylenes, olefin copolymers, polymethacrylates and polyalkylstyrenes and hydrogenated polyisoprene star polymer (Shellvis).
- suitable antifoaming agents are polydimethyl- siloxanes and polyethylene glycol ethers and esters.
- Another class of lubricant applications are industrial oil formulations, preferably turbine oils and hydraulic oils.
- Preferred formulations comprise more than 90 wt% of the base oil according to the present invention and between 0.5 and 3 wt% and preferably less than 2.5 wt% of an additive.
- the additives may be additives suited for the above applications, which are well known to one skilled in the art.
- Example 1 The invention shall be illustrated by means of the following non-limiting examples.
- Example 1 The invention shall be illustrated by means of the following non-limiting examples.
- Example 1 illustrates the process to prepare a base oil having a higher cyclo-paraffin content.
- a Fischer-Tropsch product was made having boiling curve as in Table 1 by repeating Example VII of WO-A-9934917 using the catalyst as prepared in
- the feed contained about 60 wt% C30+ product.
- the ratio Cgn+/ 30 + was about 0.55.
- the Fischer-Tropsch product as thus obtained was continuously fed to a hydrocracking step (step (a) ) .
- step (a) the Fischer-Tropsch product and a recycle stream consisting of the 370 °C + fraction of the effluent of step (a) was contacted with a hydrocracking catalyst of Example 1 of EP-A-532118 at a reactor temperature of 330 °C .
- the Fischer-Tropsch product WHSV was contacted at 0.8 kg/l.h and the recycle stream was contacted at 0.2 kg/l.h at a total pressure of 35 bar and a hydrogen partial pressure of 33 bar.
- the recycle gas rate was 2000 Nl/kg of total feed.
- the conversion of compounds boiling above 370 °C in the total feed which were converted to products boiling below 370 °C was 55 wt%.
- the product of the hydrocracking step was distilled into one or more fuels fractions boiling in the naphtha, kerosene and gas oil range and a bottom product boiling above 370 °C .
- the 370 °C + fraction thus obtained was in turn distilled in a vacuum distillation column, wherein the feed rate to the column was 750 g/h, the pressure at the top was kept at 0.4 mm Hg (0.5 mbar) and the temperature at the top was kept at 240 °C, which is equal to an atmospheric cut off temperature of 515 °C.
- the top product had thus a boiling range of between 370 and 515 °C. Further properties were a pour point of +18 °C and a kinematic viscosity at 100 °C of 3.8 cSt. This top product was further used as the base oil precursor fraction in step (c) .
- the base oil precursor fraction was contacted with a dealuminated silica bound ZSM-5 catalyst comprising 0.7% by weight Pt and 30 wt% ZSM-5 as described in Example 9 of WO-A-0029511.
- the dewaxed oil was distilled, wherein a lighter and a heavier fraction was removed to obtain the final base oil having the improved solvency properties and the properties as listed in Table 2.
- Example 1 was repeated except that the dewaxed oil was distilled differently to yield the base oil having the improved solvency properties and other properties as listed in Table 3.
- Table 3
- Example 3 shows that a base oil as obtained by the present invention can be successfully used to formulate OW-30 motor gasoline lubricants using the same additives as used to formulate such a grade based on poly-alpha olefins .
- Base oils as prepared from the same feed as in Examples 1 and 2 under varying conditions were prepared. Properties are listed in Table 6.
- the cyclo-paraffins and normal and iso-paraffins of the base oil of Example 5 were further analysed.
- Figure 1 the content of the normal and iso-paraffins, 1-ring cyclo- paraffins, 2-ring cyclo-paraffins, etc, in the saturates phase as a function of their respective carbon numbers are shown of this base oil.
Abstract
Description
Claims
Priority Applications (12)
Application Number | Priority Date | Filing Date | Title |
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JP2002565028A JP2004521976A (en) | 2001-02-13 | 2002-02-13 | Base oil composition |
DE60206891T DE60206891T2 (en) | 2001-02-13 | 2002-02-13 | BASE OIL COMPOSITION |
AT02740082T ATE307865T1 (en) | 2001-02-13 | 2002-02-13 | BASE OIL COMPOSITION |
US10/467,731 US7531081B2 (en) | 2001-02-13 | 2002-02-13 | Base oil composition |
NZ526900A NZ526900A (en) | 2001-02-13 | 2002-02-13 | Lubricating base oil composition having improved solvency properties |
EA200300878A EA006657B1 (en) | 2001-02-13 | 2002-02-13 | Base oil composition and use thereof |
BR0207092-8A BR0207092A (en) | 2001-02-13 | 2002-02-13 | Lubricating base oil composition, process for preparing a lubricating base oil, lubricating formulation and industrial formulation, and use of a formulation |
EP02740082A EP1368446B1 (en) | 2001-02-13 | 2002-02-13 | Base oil composition |
MXPA03007160A MXPA03007160A (en) | 2001-02-13 | 2002-02-13 | Base oil composition. |
CA002437858A CA2437858A1 (en) | 2001-02-13 | 2002-02-13 | Base oil composition |
AU2002308283A AU2002308283B2 (en) | 2001-02-13 | 2002-02-13 | Base oil composition |
NO20033559A NO20033559L (en) | 2001-02-13 | 2003-08-12 | Basissmöreolje |
Applications Claiming Priority (6)
Application Number | Priority Date | Filing Date | Title |
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EP01301272.9 | 2001-02-13 | ||
EP01301272 | 2001-02-13 | ||
EP01400562.3 | 2001-03-05 | ||
EP01400562 | 2001-03-05 | ||
EP01402181.0 | 2001-08-16 | ||
EP01402181 | 2001-08-16 |
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WO2002064710A2 true WO2002064710A2 (en) | 2002-08-22 |
WO2002064710A3 WO2002064710A3 (en) | 2003-10-16 |
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PCT/EP2002/001352 WO2002064711A1 (en) | 2001-02-13 | 2002-02-08 | Lubricant composition |
PCT/EP2002/001634 WO2002064710A2 (en) | 2001-02-13 | 2002-02-13 | Base oil composition |
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PCT/EP2002/001352 WO2002064711A1 (en) | 2001-02-13 | 2002-02-08 | Lubricant composition |
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US (2) | US7670996B2 (en) |
EP (2) | EP1370633B1 (en) |
JP (2) | JP2004521977A (en) |
AR (1) | AR032803A1 (en) |
AT (2) | ATE302258T1 (en) |
AU (2) | AU2002249198B2 (en) |
BR (2) | BR0207091A (en) |
CA (2) | CA2437862A1 (en) |
DE (2) | DE60205596T2 (en) |
DK (2) | DK1370633T3 (en) |
EA (1) | EA006657B1 (en) |
ES (2) | ES2248538T3 (en) |
MX (2) | MXPA03007088A (en) |
MY (1) | MY128885A (en) |
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