Classifications

• • 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
  • C10M111/00—Lubrication compositions characterised by the base-material being a mixture of two or more compounds covered by more than one of the main groups C10M101/00 - C10M109/00, each of these compounds being essential
  • C10M111/04—Lubrication compositions characterised by the base-material being a mixture of two or more compounds covered by more than one of the main groups C10M101/00 - C10M109/00, each of these compounds being essential at least one of them being a macromolecular organic compound
• • 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
  • C10M177/00—Special methods of preparation of lubricating compositions; Chemical modification by after-treatment of components or of the whole of a lubricating composition, not covered by other classes
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
  • C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
  • C10G2300/10—Feedstock materials
  • C10G2300/1022—Fischer-Tropsch products
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
  • C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
  • C10G2300/20—Characteristics of the feedstock or the products
  • C10G2300/201—Impurities
  • C10G2300/202—Heteroatoms content, i.e. S, N, O, P
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
  • C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
  • C10G2300/20—Characteristics of the feedstock or the products
  • C10G2300/30—Physical properties of feedstocks or products
  • C10G2300/301—Boiling range
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
  • C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
  • C10G2300/20—Characteristics of the feedstock or the products
  • C10G2300/30—Physical properties of feedstocks or products
  • C10G2300/302—Viscosity
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
  • C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
  • C10G2300/20—Characteristics of the feedstock or the products
  • C10G2300/30—Physical properties of feedstocks or products
  • C10G2300/304—Pour point, cloud point, cold flow properties
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
  • C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
  • C10G2300/20—Characteristics of the feedstock or the products
  • C10G2300/30—Physical properties of feedstocks or products
  • C10G2300/308—Gravity, density, e.g. API
• • 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
• • 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
  • C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
  • C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
  • C10M2203/1006—Petroleum or coal fractions, e.g. tars, solvents, bitumen used as base material
• • 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
• • 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
• • 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
  • C10N2020/00—Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
  • C10N2020/01—Physico-chemical properties
  • C10N2020/011—Cloud point
• • 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
  • C10N2020/00—Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
  • C10N2020/01—Physico-chemical properties
  • C10N2020/02—Viscosity; Viscosity index
• • 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
  • C10N2020/00—Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
  • C10N2020/01—Physico-chemical properties
  • C10N2020/071—Branched chain compounds
• • 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
• • 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
  • C10N2030/70—Soluble oils
• • 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
  • C10N2070/00—Specific manufacturing methods for lubricant compositions

Definitions

• the invention relates to a lubricating base oil blend
• a lubricating base oil blend comprising (a) a mineral oil derived base oil having a saturates content of more than 90 wt%, a sulphur content of less than 0.03 wt% and a viscosity index (VI) of between 80-150 and a (b) a Fischer-Tropsch derived paraffinic base oil component having a kinematic viscosity at 100 0 C of from 7 to 30 Cst (7 to 30 mm 2 /s) . It further relates to a process for the preparation of such blends .
• a mineral oil derived base oil having a saturates content of more than 90 wt%, a sulphur content of less than 0.03 wt% and a viscosity index (VI) of between 80-150 and a
• a Fischer-Tropsch derived paraffinic base oil component having a kinematic viscosity at 100
• the maximum achievable viscosity for either Group II and Group III base oils is defined by the origin and composition of the crude distillate or slack-wax feed employed. This is due to the fact that no molecular weight build-up during the preparation, and hence the maximum molecular weights and thus the related viscosity cannot be higher than of the high molecular weight compounds already present in the feed. Furthermore, during hydrotreatment or hydroprocessing steps the molecular weight of the obtained products is constantly reduced due to cracking reactions, as well as the structure of the compounds.
• a blend comprising a distillate base oil having a saturates content of more than 90 wt% and a residual Fischer-Tropsch derived paraffinic base oil component is disclosed in US-A-7053254.
• the desired kinematic viscosity range at 100 0 C could not be achieved with blends that were clear and bright at ambient temperature for a prolonged period of time.
• PAO highly viscous polyalphaolefin
• a further object of the present invention resides in providing for a process for the manufacture of such blends .
• a lubricating base oil blend comprising (a) a mineral oil derived base oil having a saturates content of more than 90 wt%, a sulphur content of less than 0.03 wt% and a viscosity index of between 80-150, and (b) a paraffinic base oil component having a viscosity at 100 0 C of from 7 to 30 cSt, wherein component (b) is an isomerised
• FIG. 1 illustrates the cloud points of a number of blends of a a mineral derived Gp II base oil (a) with a paraffinic Fischer-Tropsch derived residual base oil components (b) from 1 to 10 %wt . Also the cloud points are shown. On the x-axis are shown the %wt GTL extra heavy base oil (XHBO) in blend with 12 cSt Gp II base oil. On the y-axis the temperature is shown ( 0 C) . All blends were clear and bright by definition since all cloud points were negative.
• XHBO %wt GTL extra heavy base oil
• lubricating base oils which are used for example to formulate engine lubricants and industrial oils, are normally prepared from suitable mineral oil feedstock by a variety of refining processes which are generally directed to obtaining a lubricating base oil with a predetermined set of properties, for example viscosity, oxidation stability and maintenance of fluidity over a wide range of temperatures (as indicated by viscosity index) .
• the preparation of lubricating base oils is conventionally carried out as follows: A mineral crude oil is separated by distillation at atmospheric pressure into a number of distillate fractions and a residue, known as long residue. The long residue is then separated by distillation at reduced pressure into a number of vacuum distillates and a vacuum residue known as short residue.
• lubricating base oils are prepared by refining processes. By these processes aromatics and wax are removed or chemically converted to acceptable distillate base oil molecular components from the vacuum distillate fractions. From the short residue asphalt can be removed by known deasphalting processes. From the deasphalted oil thus obtained aromatics and wax can subsequently be removed to yield a residual lubricating base oil, known as bright stock. The wax obtained during refining of the various lubricating base oil fractions is designated as "slack wax". Lubricating base oils are usually obtained from suitable vacuum distillate fractions and/or from deasphalted oil by suitable refining processes, including catalytic and solvent upgrading and dewaxing processes and catalytic hydrotreatment .
• Mineral crude oil derived lubricating base oils are also referred to as a API Group I, II or III base oils as defined in API Publication 1509: Engine Oil Licensing and Certification System, "Appendix E-API Base Oil Inter- changeability Guidelines for Passenger Car Motor Oil and Diesel Engine Oils". In an article in the Oil & Gas
• API Group-II base oils are described. All of the possible routes will involve at one point the solvent extraction or hydrogenation of the aromatic and other unsaturated compounds to obtain a base oil having the desired saturates content. Such a hydrogenation will typically be performed by contacting the feed with hydrogen in the presence of a hydrogenation catalyst, typically a Group VIII metal supported catalyst, as for instance described in US-A-5935416. While it is possible to obtain API Group II base oils in this way, API Group III base oils, i.e. having a viscosity index of at least 120 are more difficult to obtain directly by such processes.
• a hydrogenation catalyst typically a Group VIII metal supported catalyst
• API Group III lubricating base oils can be obtained directly from high wax containing feedstocks derived from waxy crude oils, by a process comprising contacting a hydrocarbonaceous feedstock derived from a waxy crude oil with a hydroisomerisation catalyst under hydroisomerising conditions and subsequently recovering a lubricating base oil having a high viscosity index. Such a process is for instance described in EP-A-0400742.
• the maximum obtainable kinematic viscosity of such base oils is determined by their maximum carbon number as expressed by the average number molecular weight and the molecular weight distribution of the feeds.
• the mineral derived base oil component (a) is preferably present in an amount of from 40 wt% to 98 wt%, based on the total weight of the oil blend, more preferably of from 50 to 97 wt%, more preferably of from 60 to 96 wt%, more preferably of from 70 to 95 wt%, more preferably of from 80 to 94 wt%, and more preferably of from 90 to 93 wt% .
• the remainder is the paraffinic base oil component (b) .
• the base oil blend component (a) preferably has a kinematic viscosity at 100 0 C of greater than 12.0 cSt, more preferably greater than 15.0 cSt still more preferably above 20.0 cSt, and a viscosity index of greater than 95, more preferably greater than 100.
• the viscosity index of component (a) is preferably between 100 and 110, but may be relaxed due to the high VI contribution of the component (b) .
• the base oil blend according to the invention preferably has a cloud point of below 0 0 C.
• component (a) is an API Group II and/or an API Group III base oils as defined in API Publication 1509.
• the Fischer-Tropsch derived paraffinic heavy base oil component (b) is a heavy hydrocarbon composition comprising at least 95 wt% paraffin molecules.
• the heavy base oil component (b) of the invention is prepared from a Fischer-Tropsch wax and comprises more than 98 wt% of saturated, paraffinic hydrocarbons.
• at least 85 wt%, more preferably at least 90 wt%, yet more preferably at least 95 wt%, and most preferably at least 98 wt% of these paraffinic hydrocarbon molecules are isoparaffinic .
• at least 85 wt% of the saturated, paraffinic hydrocarbons are non-cyclic hydrocarbons.
• Naphthenic compounds are preferably present in an amount of no more than 15 wt%, more preferably less than 10 wt%.
• the Fischer-Tropsch derived paraffinic base oil component (b) contains hydrocarbon molecules having consecutive numbers of carbon atoms, such that it comprises essentially a continuous series of consecutive iso-paraffins, i.e. iso-paraffins having n, n+1, n+2, n+3 and n+4 carbon atoms. These consecutive numbers of carbon atoms is a consequence of the Fischer-Tropsch hydrocarbon synthesis reaction from which the wax feed, which has been subjected to isomerisation to form component (b) .
• Component (b) further is a liquid at 100 0 C and under ambient conditions, i.e. at 25°C and one atmosphere (101 kPa) absolute pressure.
• the heavy hydrocarbon composition is typically a liquid at the temperature and pressure conditions of use and typically, but not always, at ambient conditions of 24°C and one atmosphere (101 kPa) pressure.
• the kinematic viscosity at 100 0 C (VKlOO) of component (b), as measured according to ASTM D-445, is at least 7 cSt (7 mm ⁇ /s) .
• the kinematic viscosity of the heavy hydrocarbon compositions of the invention at 100 0 C (VKlOO) is at least 10 cSt, more preferably at least 13 cSt, yet more preferably at least 15 cSt, again more preferably at least 17 cSt, yet again amore preferably at least 20 cSt, and most preferably at least 25 cSt .
• the initial and end boiling points values referred to herein are nominal and refer to the T5 and T95 cut-points (boiling temperatures) obtained by gas chromatograph simulated distillation (GCD), using methods set out above .
• Component (b) preferably has an initial boiling point of at least 400 0 C. More preferably, the initial boiling point is at least 450 0 C, yet more preferably at least 480 0 C, more preferably more than 500 0 C, yet more preferably more than 540 0 C.
• the 10 wt% recovery point refers to that temperature at which 10 wt% of the hydrocarbons present within that cut will vaporize at atmospheric pressure, and could thus be recovered.
• the 90 wt% recovery point refers to the temperature at which 90 wt% of the hydrocarbons present will vaporize at atmospheric pressure.
• Component (b) preferably according to the invention contains molecules having consecutive numbers of carbon atoms and preferably at least 95 wt% C30+ hydrocarbon molecules. More preferably, component (b) preferably contains at least 75 wt% of C35+ hydrocarbon molecules.
• Cloud point refers to the temperature at which a sample begins to develop a haze, as determined according to ASTM D-5773. Component (b) typically has a cloud point between - 60 0 C and + 49°C.
• component (b) preferably has a pour point of below -28°C. Furthermore, in the base oil blend according to the invention, component (b) preferably has no measurable pour point depressing effect on the base oil blend, such that the pour points of the base oil blend is intermediate between those of the components (a) and (b) and not lower than either component (a) and (b) .
• component (b) has a cloud point between 30 0 C and - 55°C, more preferably between 10 0 C and - 50 0 C. It was found that depending on the feed and the dewaxing conditions, some of the Fischer-Tropsch derived paraffinic heavy base oil component (b) would have a cloud point above ambient temperature, while other properties were not negatively affected.
• Pour point refers to the temperature at which a base oil sample will begin to flow under carefully controlled conditions .
• the pour points referred to herein were determined according to ASTM D 97-93.
• Molecular weights were determined according to ASTM D-2503.
• Viscosity index (VI) was determined by using ASTM D-2270.
• the component (b) according to the subject invention preferably has a viscosity index of between 120-170, more preferably from 135 to 165, yet more preferably from 150 to 160.
• Component (b) preferably 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.
• component (b) comprises sulphur, nitrogen and metals in the form of hydrocarbon compounds containing in amounts of less than 50 ppmw, more preferably less than 20 ppmw, yet more preferably less than 10 ppmw. Most preferably it will comprise sulphur and nitrogen at levels generally below the detection limits, which are currently 5 ppm for sulphur and 1 ppm for nitrogen when using for instance by X-ray or Antek Nitrogen tests for determination.
• sulphur may be introduced through the use of sulphided hydrocracking/hydrodewaxing and/or sulphided catalytic dewaxing catalysts.
• the Fischer-Tropsch derived paraffinic base oil component (b) in the present invention is preferably separated as residual fraction from the hydrocarbons produced during a Fischer-Tropsch synthesis reaction and subsequent hydrocracking and dewaxing steps . More preferably this fraction is a distillation residue comprising the highest molecular weight compounds still present in the product of the hydroisomerisation step.
• the 10 wt% recovery boiling point of said fraction is preferably above 370 0 C, more preferably above 400 0 C and most preferably above 500 0 C for certain embodiments of the present invention.
• the Fischer-Tropsch derived paraffinic base oil component (b) can further be specified by its content of different carbon species. More particular, the Fischer-Tropsch derived paraffinic base oil component (b) can be specified by the percentage of its epsilon methylene carbon atoms, i.e. the percentage of recurring methylene carbons which are four or more carbons removed from an end group and a branch (further referred to as CH2>4) as compared to the percentage of isopropyl carbon atoms.
• isomerised Fischer-Tropsch bottoms products as disclosed in US-A-7053254 differ from the Fischer-Tropsch derived paraffinic base oil components according to the present invention, which are usually obtained at a higher dewaxing severity in that the latter compounds have a ratio of percentages epsilon methylene carbon atoms to carbon atoms in isopropyl branches of at or above 8.2, as measured on the Fischer Tropsch base oil as a whole. It has been in particular found that a Fischer-Tropsch product as disclosed in US-A-7053254 with a mild degree of isomerisation was not suitable for addition in amounts larger than 1.5 to 2 wt% due to its inability to achieve clear and bright blend.
• the branching properties as well as the carbon composition of the Fischer-Tropsch derived base oil blending components can conveniently be determined by analyzing a sample of oil using C- ⁇ -NMR, vapour pressure osmometry (VPO) and Field Ionization Mass Spectrometric
• FIMS Field ionization mass spectrometry
• VPO vapour pressure osmometry
• NMR nuclear magnetic resonance
• VPO the average number of branches and aliphatic rings can be calculated. Further, on the basis of GASPE, the distribution of side chain lengths and the positions of the methyl groups along the straight chain were obtained. Quantitative carbon multiplicity analysis is normally carried out entirely at room temperature. However this is only applicable to materials which are liquid under these conditions . This method is applicable to any synthetic (e.g. Fischer-Tropsch) derived or mineral derived base oil material which is hazy or a waxy solid at room temperature, and therefore cannot be run by the normal method. The methodology for the NMR measurements was as follows: As solvent for determination of quantitative carbon multiplicity analysis, deuterated chloroform (CDCI3) was employed, limiting the maximum measurement temperature to 50 0 C for practical reasons.
• CDCI3 deuterated chloroform
• a base oil sample is heated in an oven at 50 0 C until it forms a clear and liquid homogeneous product.
• a portion of the sample is then transferred into an NMR tube.
• the NMR tube and any apparatus used in the transfer of the sample is kept at this temperature.
• the above-identified solvent is then added and the tube shaken to dissolve the sample, optionally involving reheating of the sample.
• the NMR instrument is maintained at 50 0 C during acquisition of the data.
• the sample is placed in the NMR instrument for a minimum of 5 minutes is required for the temperature to equilibrate. After this the instrument must be re-shimmed and re-tuned as both these adjustments will change considerably at the elevated temperature, and the NMR data could now be acquired.
• a CH3 subspectrum was obtained using the GASPE pulse sequence, obtained by addition of a CSE spectrum (standard spin echo) to a 1/J GASPE (gated acquisition spin echo) .
• the resultant spectrum contains primary (CH3) and tertiary carbon (CH) peaks only.
• Distinct intense signals in the region of 22 to 24 ppm can be unambiguously identified as isopropyl end groups of the following general structure (see Formula 2) .
• one of the methyl carbon atoms is classified as termination of the main chain, the other as being a branch. Therefore when calculating methyl branch content the intensity of these signals is halved. d. Further, several weak signals in the region of 15 to 19 ppm are considered to belong to isopropyl group with an additional branch in the 3 position. e. Observed in the spectrum are some weak signals in the region 8 to 8.5 ppm, most likely pertaining to 3,3- dimethyl substituted structures (Formula 3) :
• the observed signal is for the terminal CH3, but there are two corresponding methyl branches.
• the overall theoretical terminal CH3 content was calculated based on the "Z" content and the average carbon number, as determined by FIMS.
• the C3+ branch content is then determined by subtracting from the theoretical terminal CH3 content the known terminal CH3 contents i.e. half of the isopropyl value, the 3-methyl substituted value and the value for 3,3-dimethyl substituted structures, thereby resulting in a value for the signals in the 14 ppm region which belong to CH3's terminating the chain, the difference being the value for the C3+ branches:
• ⁇ (integrals C3+ branches) Int 14-15 ppm - ( (theoretical terminal CH 3 ) - (Int 11.2 to 11.8 ppm) - (Int 22 to 25 ppm) /2 - Int 7 to 9 ppm) ) .
• the present invention further relates to a process for the preparation of a lubricant base oil blend, comprising blending
• component (b) a paraffinic base oil component having a viscosity at 100 0 C of from 7 to 30 cSt (7 to 30 mm 2 /s), wherein component (b) is an isomerised Fischer-Tropsch derived bottoms product having a ratio of percentage of recurring methylene carbons which are four or more carbons removed from an end group and a branch to the percentage of isopropyl carbon atoms , as determined by 13 C-NMR, of below 8,2.
• the present invention also relates to a process for the preparation of a lubricating base oil having a saturates content of more than 90 wt%, a sulphur content of less than 0.03 wt%, a viscosity index of between 80-150, comprising (a) contacting a mineral oil derived feed as described above with hydrogen in the presence of a hydrogenation catalyst, and (b) blending of the obtained product with a Fischer-Tropsch derived component (b) according to any one of claims 1 to 7. More preferably, the above process comprises the steps
• step (ii) separating the effluent of step (i) into a gaseous fraction and a liquid fraction, wherein the liquid fraction has a sulphur content of between 50 and 1000 ppmw and a nitrogen content of less than 50 ppmw;
• step (iii) contacting the liquid fraction of step (ii) with a catalyst comprising a noble metal component supported on an amorphous refractory oxide carrier in the presence of hydrogen in a second hydrotreating step;
• step (v) blending the base oil obtained in step (iv) with the paraffinic base oil component (b) .
• the hydrotreating catalyst in step (i) comprises at least one Group VIB metal component and a metal selected from the group consisting of iron, nickel and cobalt and a refractory oxide support .
• the catalyst of step (i) is a nickel/molybdenum on alumina catalyst having a nickel content 1-5 wt% as oxide and a molybdenum content of between 10-30 wt% as oxide.
• the catalyst of step (iii) comprises platinum and palladium and an amorphous silica/alumina support, wherein the total amount of platinum and palladium is between 0.2 and 5 wt%.
• the lubricating base oil product is obtained by solvent extraction of a petroleum fraction boiling in the lubricating oil range, followed by solvent dewaxing and/or catalytic dewaxing.
• the lubricating base oil product is an API Group I base oil and the product obtained in step (d) is an API Group II or Group III base oil.
• the paraffinic base oil component (b) is a heavy bottom heavy bottom distillate fraction obtained from a Fischer-Tropsch derived wax or waxy raffinate feed by:
• step (b) separating the product of step (a) into one or more distillate fraction (s) and a residual heavy fraction comprising at least 10% wt . of compounds boiling above 540 0 C;
• step (d) isolating from effluent of step (c) as a residual heavy fraction the Fischer-Tropsch derived paraffinic base oil component.
• the paraffinic base oil component (b) is a heavy bottom heavy bottom distillate fraction obtained from a Fischer-Tropsch derived wax or waxy raffinate feed by: a) hydrocracking/hydroisomerisating a Fischer- Tropsch derived feed, wherein weight ratio of compounds having at least 60 or more carbon atoms and compounds having at least 30 carbon atoms in the Fischer-Tropsch derived feed is at least 0.2 and wherein at least 30 wt% of compounds in the Fischer-Tropsch derived feed have at least 30 carbon atoms;
• step (b) separating the product of step (a) into one or more distillate fraction (s) of lower boiling fractions and a broad range base oil precursor fraction and a heavy fraction such that the T90 wt% boiling point of the base oil precursor fraction is between 350 and 550 0 C;
• step (c) performing a pour point reducing step to the broad range base oil precursor fraction obtained in step (b) ;
• step (d) isolating the heavy bottom distillate fraction by distilling the product of step (c) .
• the Fischer-Tropsch derived product fractions may undergo various other operations, such as hydrocracking, hydrotreating, and hydrofinishing.
• the feed of step (a) is a Fischer-Tropsch derived product.
• the initial boiling point of the Fischer-Tropsch product may range up to 400 0 C, but is preferably below 200 0 C.
• any compounds having 4 or less carbon atoms and any compounds having a boiling point in that range are separated from a Fischer-Tropsch synthesis product before the Fischer-Tropsch synthesis product is used in said hydroisomerisation step.
• An example of a suitable Fischer-Tropsch process is described in
• 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 limits, which are currently 5 ppm for sulphur and 1 ppm for nitrogen.
• the Fischer-Tropsch product can be obtained by well- known processes, for example the so-called Sasol process, the Shell Middle Distillate Process or by the ExxonMobil "AGC-21" process.
• the process will generally comprise a Fischer-Tropsch synthesis and a hydroisomerisation step as described in these publications.
• the Fischer-Tropsch synthesis can be performed on synthesis gas prepared from any sort of hydrocarbonaceous material such as coal, natural gas, biological matter such as wood or hay.
• the Fischer-Tropsch product directly obtained from a Fischer-Tropsch process contains a waxy fraction that is normally a solid at room temperature.
• the Fischer-Tropsch wax used as the feed for the present process is obtained via the well-known Fischer- Tropsch hydrocarbon synthesis process.
• Fischer-Tropsch hydrocarbon synthesis involves the preparation of hydrocarbons from a mixture of carbon monoxide and hydrogen at elevated temperature and pressure in the presence of a suitable catalyst.
• the Fischer-Tropsch catalyst normally is selective for preparing paraffinic molecules, mostly straight-chain paraffins, and the product from a Fischer-Tropsch synthesis reaction therefore usually is a mixture of a large variety of paraffinic molecules.
• hydrocarbons that are gaseous or liquid at room temperature are recovered separately, for instance as fuel gas (C5-), solvent feedstocks and detergent feedstocks (up to C17) .
• the heavier paraffins (C18+) are recovered as one or more wax fractions, commonly referred to as Fischer-Tropsch wax(es) or synthetic wax(es) .
• Fischer-Tropsch wax(es) or synthetic wax(es) are recovered as the feed, which meet the aforementioned requirements with respect to their boiling range and congealing point.
• Fischer-Tropsch wax feeds are those having a congealing point in the range of from 55 to 150 0 C, more preferably from 60 to 120 0 C and/or such boiling range that the T90-T10 is in the range of from 50 to 130 0 C.
• Fischer-Tropsch waxes melting below 100 0 C suitably have a kinematic viscosity at 100 0 C
• VkIOO VkIOO of at least 3 cSt (3 mm 2 /s), preferably between 3 and 12 cSt, more preferably between 4 and 10 cSt.
• Those Fischer-Tropsch waxes melting above 100 0 C suitably have a kinematic viscosity at a temperature T, which is 10 to 20 0 C higher than their melting point, in the range of from 8 to 15 cSt, preferably from 9 to 14 cSt .
• the feed to the hydroisomerisation step is preferably a Fischer-Tropsch product which 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. Furthermore the weight ratio of compounds having more than 30 to at least 60 or more carbon atoms to compounds having at least 30 carbon atoms to less than 60 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
• the Fischer- Tropsch wax feed for step (a) has a weight ratio of compounds having at least 60 or more carbon atoms and compounds having at least 30 carbon atoms in the Fischer- Tropsch derived feed is at least 0.2, more prefably at least 0.4.
• the hydrocracking/hydroisomerisation reaction of the hydroisomerisation 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 the hydroisomerisation typically comprise an acidic functionality and a hydrogenation - dehydrogenation functionality.
• Preferred acidic functionality's 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 supported on a silica-alumina carrier.
• the catalyst does not contain a halogen compound, such as for example fluorine, because the use of such catalysts require special operating conditions and involve environmental problems. Examples of suitable hydrocracking/hydroisomerisation processes and suitable catalysts are described in WO-A-0014179, EP-A-532118, EP-A-666894 and the earlier referred to EP-A-776959.
• Preferred hydrogenation - dehydrogenation functionality's are Group VIII metals, for example cobalt, nickel, palladium and platinum and more preferably platinum.
• 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.
• nickel a higher content will be present, optionally nickel is used in combination with copper.
• 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.
• the temperatures typically will be in the range of from 175 to 380 0 C, preferably higher than 250 0 C and more preferably from 300 to 370 0 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 the hydroisomerisation as defined as the weight percentage of the feed boiling above 370 0 C which reacts per pass to a fraction boiling below 370 0 C, is at least 20 wt%, preferably at least 25 wt%, but preferably not more than 80 wt%, more preferably not more than 70 wt% .
• the feed as used above in the definition is the total hydrocarbon feed fed to the hydroisomerisation, thus also any optional recycle to step (a) .
• the resulting product of the hydroisomerisation process preferably contains at least 50 % by weight of iso-paraffins, more preferably at least 60 % by weight , yet more preferably at least 70 % by weight of iso- paraffins, the remainder being composed of n-paraffins and naphthenic compounds .
• step (b) the product of step (a) is separated into one or more distillate fraction (s) and a residual heavy fraction comprising at least 10% wt . of compounds boiling above 540 0 C.
• step (c) This is conveniently done by performing one or more distillate separations on the effluent of the hydroisomerisation step to obtain at least one middle distillate fuel fraction and a residual fraction which is to be used in step (c) .
• the effluent of step (a) is first subjected to an atmospheric distillation.
• the residue as obtained in such a distillation is may in certain preferred embodiments be subjected to a further distillation performed at near vacuum conditions to arrive at a fraction having a higher 10 wt% recovery boiling point.
• the 10 wt% recovery boiling point of the residue may preferably vary between 350 and 550 0 C.
• This atmospheric bottom product or residue preferably boils for at least 95 wt% above 370 0 C.
• This fraction may be directly used in step (c) or may be subjected to an additional vacuum distillation suitably performed at a pressure of between 0.001 and 0.1 bara.
• the feed for step (c) is preferably obtained as the bottom product of such a vacuum distillation.
• the heavy residual fraction obtained in step (b) is subjected to a catalytic pour point reducing step.
• Step (c) may be performed using any hydroconversion process, which is capable of reducing the wax content to below 50 wt % of the original wax content.
• the wax content in the intermediate product is preferably below 35 wt% and more preferably between 5 and 35 wt%, and even more preferably between 10 and 35 wt%.
• the product as obtained in step (c) preferably has a congealing point of below 80 0 C.
• Preferably more than 50 wt% and more preferably more than 70 wt% of the intermediate product boils above the 10 wt% recovery point of the wax feed used in step (a) .
• the wax content as used in the description is measured according to the following procedure.
• 1 weight part of the to be measured oil fraction is diluted with 4 parts of a (50/50 vol/vol) mixture of methyl ethyl ketone and toluene, which is subsequently cooled to -20 0 C in a refrigerator.
• the mixture is subsequently filtered at -20 0 C.
• the wax is thoroughly washed with cold solvent, removed from the filter, dried and weighed. If reference is made to oil content a wt% value is meant which is 100% minus the wax content in wt%.
• a possible process is the hydroisomerisation process as described above for step (a) . It has been found that the wax may be reduced to the desired level using such catalyst. By varying the severity of the process conditions as described above a skilled person will easily determine the required operating conditions to arrive at the desired wax conversion. However a temperature of between 300 and 330 0 C and a weight hourly space velocity of between 0.1 and 5, more preferably between 0.1 and 3 kg of oil per litre of catalyst per hour (kg/l/hr) are especially preferred for optimising the oil yield.
• a more preferred class of catalyst which may be applied in step (c), is the class of dewaxing catalysts.
• the process conditions applied when using such catalysts should be such that a wax content remains in the oil.
• typical catalytic dewaxing processes aim at reducing the wax content to almost zero.
• Using a dewaxing catalyst comprising a molecular sieve will result in that more of the heavy molecules are retained in the dewaxed oil. Thus a more viscuous base oil can then be obtained.
• the dewaxing catalyst which may be applied in step (c) suitably comprises a molecular sieve and optionally in combination with a metal having a hydrogenation function, such as the Group VIII metals.
• a metal having a hydrogenation function such as the Group VIII metals.
• Molecular sieves, and more suitably molecular sieves having a pore diameter of between 0.35 and 0.8 nm have shown a good catalytic ability to reduce the wax content of the wax feed.
• Suitable zeolites are mordenite, beta, ZSM-5, ZSM-12, ZSM-22, ZSM-23, SSZ-32, ZSM-35 and ZSM-48 or combinations of said zeolites, of which ZSM-12 and ZSM-48 area most preferred.
• SAPO silica-aluminaphosphate
• SAPO-Il 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 Pt/ZSM-35, Ni/ZSM-5, Pt/ZSM-23, Pd/ZSM-23, Pt/ZSM-48 and Pt/SAPO-11 or stacked configurations of Pt/zeolite beta and Pt/ZSM-23, Pt/zeolite beta and Pt/ZSM-48 or Pt/zeolite beta and Pt/ZSM-22.
• suitable molecular sieves and dewaxing conditions are for example described in WO-A-9718278, US-A-4343692, US-A-5053373, US-A-5252527, US-A-20040065581, US-A-4574043 and EP-A-1029029.
• Another preferred class of molecular sieves are those having a relatively low isomerisation selectivity and a high wax conversion selectivity, like ZSM-5 and ferrierite (ZSM-35) .
• 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. Examples of these 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 refractory oxide of which examples are: alumina, silica-alumina, 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 f luorosilicate salt as described in for example US-A-5157191 or WO-A-0029511.
• dewaxing catalysts as described above are silica bound and dealuminated Pt/ZSM-5, silica bound and dealuminated Pt/ZSM-35 as for example described in WO-A-0029511 and EP-B-832171.
• the conditions in step (c) when using a dewaxing catalyst typically involve operating temperatures in the range of from 200 to 500 0 C, suitably from 250 to 400 0 C. Preferably the temperature is between 300 and 330 0 C.
• the 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 0.1 to 5 kg/l/hr, more suitably from 0.1 to
• WHSV weight hourly space velocities
• step (c) It was found that when a dewaxing severity of about 30% per pass had been surpassed in step (c), the yield and pour point dropped exponentially until a further plateau was reached at a pour point in the range of from -50 to -60 0 C. It was further found that isomerised Fischer-Tropsch derived bottoms products obtained that had a pour point of below -28°C were found to show a much reduced pour point reducing effect, or were no longer pour point depressing.
• step (d) the product of step (c) is usually sent to a vacuum column where the various distillate base oil cuts are collected.
• These distillate base oil fractions may be used to prepare lubricating base oil blends, or they may be cracked into lower boiling products, such as diesel or naphtha.
• the residual material collected from the vacuum column comprises a mixture of high boiling hydrocarbons, and is used to prepare component (b) of the present invention.
• step (c) may also be subjected to additional treatments, such as solvent dewaxing.
• the product obtained in the process according to the present invention can be further treated, for example in a clay treating process or contacting with active carbon, as for example described in US-A-4795546 and EP-A-712922, in order to improve the stability. It was also found that the saturates level, the pour point and the VI of a Group II and III base oils could be relaxed when used in blends according to the invention, since the addition of the component (b) due to its high saturation level, very low pour point and high VI permitted to achieve targeted values of Vk 100 0 C, pour point and VI.
• the subject invention also relates to a process for the preparation of a lubricating base oil having a saturates content of more than 90 wt%, a sulphur content of less than 0.03 wt%, a viscosity index of between 80-150, comprising (a) contacting a mineral oil derived feed as described above with hydrogen in the presence of a hydrogenation catalyst, and (b) blending of the obtained product with a Fischer-Tropsch derived component (b) as obtained as set out above .
• API Group II based formulations with low additive treatment rates, and hence low additive thickening such as e.g. SAE 40 or 50 monograde gas engine oils could be achieved through blending According to the invention. This is otherwise difficult since the SAE kinematic viscosity requirement is at least 12.5 mm ⁇ /s
• MTW Type zeolite crystallites were prepared as described in "Verified synthesis of zeolitic materials” as published in Micropores and mesopores materials, volume 22 (1998), pages 644-645 using tetra ethyl ammonium bromide as the template.
• the Scanning Electron Microscope (SEM) visually observed particle size showed ZSM-12 particles of between 1 and 10 ⁇ m.
• the average crystallite size as determined by XRD line broadening technique was 0.05 ⁇ m.
• the crystallites thus obtained were extruded with a silica binder (10% by weight of zeolite, 90% by weight of silica binder) .
• the extrudates were dried at 120 0 C.
• a Fischer-Tropsch derived wax that had been subjected to a hydrocracking/hydriosmerisation treatment, and further comprised at least 80% wt . of isoparaffins having the properties as in Table 1 was distilled into a light base oil precursor fraction boiling substantially between 390 and 520 0 C and a residual heavy fraction boiling above 520 0 C.
• the residual base oil precursor fraction was contacted with the above-described dewaxing catalyst.
• the dewaxed oil was separated by distillation into a light base oil component, and a heavy base oil component having the properties listed in Table 2.
• a mineral oil derived API Group I bright stock having a viscosity index of 95, and a kinematic viscosity at 100 0 C of 32 cSt was blended with a number of Fischer- Tropsch derived base oil components according to the invention (A, B, and C), as well as a number not according to the invention (Comparative A and B), which had been obtained from a less severe dewaxing step.
• the limit at which the mixture still had a negative cloud point and hence was clear and bright was determined by making several blends of different concentration.
• the limits to which the Fischer-Tropsch derived component could be added to arrive at a clear and bright blend after several days at ambient temperature are given as clear and bright limits.
• the limit for Fischer-Tropsch derived bottom products not according to the present invention, i.e. having a ratio of wt . % of carbons in CH2>4 (from all C) to wt . % of carbons in isopropyl groups of above 8,2 was clearly below those of the Fischer- Tropsch derived components according to the invention.
• Blends were prepared with increasing amounts of the base oil and the Gp II base oil to determine the ratio at which the cloud point would become positive.
• the blends were prepared by heating a mixture of the two components to about 50 0 C under agitation until the blend become clear and bright, and by allowing the blend to cool down to ambient temperature (25°C) .
• the blends were then kept at ambient temperature for 24 hours, 3 and 7 days, upon which the appearance was checked (see Table 5) :

Landscapes

• Chemical & Material Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• General Chemical & Material Sciences (AREA)
• Oil, Petroleum & Natural Gas (AREA)
• Organic Chemistry (AREA)
• Lubricants (AREA)
• Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)

Priority Applications (1)

Applications Claiming Priority (3)

Publications (1)

Family

ID=39135175

Family Applications (1)

Country Status (8)

Families Citing this family (13)

Family Cites Families (22)

• 2008
  • 2008-08-12 JP JP2010520565A patent/JP2010535925A/ja active Pending
  • 2008-08-12 EP EP08787150A patent/EP2176388A2/en not_active Withdrawn
  • 2008-08-12 US US12/673,044 patent/US20110290702A1/en not_active Abandoned
  • 2008-08-12 SG SG2012059283A patent/SG183713A1/en unknown
  • 2008-08-12 WO PCT/EP2008/060599 patent/WO2009021958A2/en active Application Filing
  • 2008-08-12 RU RU2010109387/04A patent/RU2494140C2/ru not_active IP Right Cessation
  • 2008-08-12 CN CN200880103089.7A patent/CN101796170B/zh not_active Expired - Fee Related
  • 2008-08-12 BR BRPI0814956-9A2A patent/BRPI0814956A2/pt not_active Application Discontinuation

Non-Patent Citations (1)

Also Published As

Similar Documents

Legal Events