EP0323092A2 - Verfahren zur Hydroisomerisierung von Fischer-Tropsch-Wachs zur Herstellung von Schmieröl - Google Patents

Verfahren zur Hydroisomerisierung von Fischer-Tropsch-Wachs zur Herstellung von Schmieröl Download PDF

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Publication number
EP0323092A2
EP0323092A2 EP88311982A EP88311982A EP0323092A2 EP 0323092 A2 EP0323092 A2 EP 0323092A2 EP 88311982 A EP88311982 A EP 88311982A EP 88311982 A EP88311982 A EP 88311982A EP 0323092 A2 EP0323092 A2 EP 0323092A2
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Prior art keywords
catalyst
wax
fischer
fluoride
lubricating oil
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EP88311982A
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English (en)
French (fr)
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EP0323092A3 (en
EP0323092B1 (de
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Heather Alexis Boucher
Glen Porter Hamner
William Augusta Wachter
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ExxonMobil Technology and Engineering Co
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Exxon Research and Engineering Co
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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
    • C10G45/60—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 characterised by the catalyst used
    • C10G45/62—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 characterised by the catalyst used containing platinum group metals or compounds thereof
    • 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
    • C10G65/00—Treatment of hydrocarbon oils by two or more hydrotreatment processes only
    • C10G65/02—Treatment of hydrocarbon oils by two or more hydrotreatment processes only plural serial stages only
    • C10G65/04—Treatment of hydrocarbon oils by two or more hydrotreatment processes only plural serial stages only including only refining steps
    • C10G65/043—Treatment of hydrocarbon oils by two or more hydrotreatment processes only plural serial stages only including only refining steps at least one step being a change in the structural skeleton

Definitions

  • This invention relates to a process for producing lubricating oil from a Fischer-Tropsch wax. More particularly, it relates to a process utilizing a Group VIII metal-on-alumina catalyst for hydroisomeri­zing a hydrotreated Fischer-Tropsch wax to produce a lubricating oil having a high viscosity index and a low pour point.
  • Paraffin waxes have been isomerized over various catalysts, e.g., Group VIB and VIII catalysts of the Periodic Table of the Elements (E. H. Sargent & Co., Copyright 1964 Dyna-Slide Co.)
  • catalysts can be characterized as halogenated supported metal catalysts, e.g., a hydrogen chloride or hydrogen fluoride treated platinum-on-alumina catalyst as disclosed, e.g., in U.S. 2,668,866 to G. M. Good et al.
  • a partially vaporized wax such as one from a Fischer-Tropsch synthesis process, is mixed with hydrogen and contacted at 300°C to 500°C over a bed of supported platinum catalyst.
  • Palladium or nickel may be substituted for platinum.
  • the support may be a number of conventional carrier materials, such as alumina or bauxite.
  • the carrier material may be treated with acid, such as HCl or HF, prior to incorpo­rating the platinum.
  • acid such as HCl or HF
  • pellets of activated alumina may be soaked in a solu­tion of chloroplatinic acid, dried and reduced in hydrogen at 475°C.
  • U.S. Patent No. 2,817,693 discloses the catalyst and process of U.S. Patent No. 2,668,866 with the recommendation that the catalyst be pretreated with hydrogen at a pressure substantially above that to be used in the process.
  • U.S. Patent No. 3,268,439 relates to the conversion of waxy hydrocarbons to give products which are characterized by a higher isoparaffin content than the feedstock.
  • Waxy hydrocarbons are converted at elevated temperature and in the presence of hydrogen by contacting the hydrocarbons with a catalyst comprising a platinum group metal, a halogenatable inorganic oxide support and at least one weight percent of fluorine, the catalyst having been prepared by contacting the support with a fluorine compound of the general for­mula: where X is carbon or sulphur and Y is fluorine or hydrogen.
  • U.S. Patent No. 3,308,052 describes a hydro­isomerization process for producing lube oil and jet fuel from waxy petroleum fractions. According to this patent, product quality is dependent upon the type of charge stock, the amount of liquid hydrocarbon in the waxy charge stock and the degree of conversion to products boiling below 650°F. The greater the amount of charge stock converted to material boiling below 650°F per pass the higher the quality of jet fuel.
  • the catalyst employed in the hydroisomerization zone is a platinum group metal catalyst comprising one or more platinum, palladium and nickel on a support, such as alumina, bentonite, barite, faujasite, etc., containing chlorine and/or fluorine.
  • a heavy oil feed boiling at least partly above 900°F is hydrocracked and the oil effluent thereof is separated into fractions, including a distillate fuel and a higher boiling hydrocracked lube oil boiling range fraction.
  • the hydrocracked lubricating oil boiling range fraction is dewaxed to obtain a hydrocracked wax fraction which is hydroisomerized in the presence of a reforming catalyst and the oil effluent thereof is separated into frac­tions, including a distillate fuel and an isomerized lube oil boiling range fraction.
  • U.S. Patent No. 3,487,005 discloses a process for the production of low pour point lubricating oils by hydrocracking a high pour point waxy oil feed boiling at least partly above 700°F in at least two stages.
  • the first stage comprises a hydrocracking-­denitrofication stage, followed by a hydrocracking-­isomerization stage employing a naphtha reforming catalyst containing a Group VI metal oxide or Group VIII metal on a porous refractory oxide, such as alumina.
  • the hydrocracking isomerization catalyst may be promoted with as much as two weight percent fluo­rine.
  • U.S. Patent No. 3,709,817 describes a process which comprises contacting a paraffin hydrocarbon containing at least six carbon atoms with hydrogen, a fluorided Group VIB or VIII metal alumina catalyst and water. These catalysts are classified by the patentee as a well-known class of hydrocracking catalysts.
  • a process for producing a lubricating oil having a high viscosity index and a low pour point from a Fischer-Tropsch wax which process comprises:
  • the hydrotreating catalyst will be unsulfided
  • the catalyst employed in the hydroisomerization zone will be a fluorided plati­num-on-aluminum catalyst
  • the isomerate is contact­ed with hydrogen in the presence of a hydrogenation catalyst to reduce unsaturation of the isomerate and thereby improve its daylight and oxidation stability.
  • a Fischer-­Tropsch wax is hydrotreated under relatively high severity conditions to remove impurities and partially convert the 1050°F+ wax, followed by hydroisomerization of the hydrotreated wax, hydrofining of the isomerate to improve daylight stability, fractionation to recover a lubricating oil fraction, and dewaxing to produce a high viscosity, low pour point lubricating oil.
  • Fischer-Tropsch wax may be made as a by-pro­duct from the conversion of natural gas or gasification of coal under known conditions to a synthesis gas (CO+H2) which may then be converted by the Fischer-­Tropsch process to form gaseous and liquid hydrocarbons and a normally solid paraffin wax known as Fischer-­Tropsch wax.
  • This wax does not contain the sulfur, nitrogen or metal impurities normally found in crude oil, but is known to contain water, trace metals and a number of oxygenate compounds such as alcohols, ketones, aldehydes, etc. These oxygenate compounds have an adverse effect on the performance of the hydroisomerization/hydrocracking catalyst of the invention and it is, therefore, advantageous to produce lube oil products by the process scheme outlined in the Figure.
  • Fischer-Tropsch wax is introduced into Hydrotreater R-1 along with hydrogen and contacted therein with a hydrotreating catalyst.
  • Fischer-Tropsch wax is generally composed of about 99+% normal paraffins, with trace amounts of metals and oxygenates as impurities. It is all high melting wax, and requires considerable structural modification (normal paraffin wax is first converted to iso-paraffin wax before oil is produced).
  • Hydrotreat­ing serves a dual purpose, namely, removal of the impurities and conversion of some of the Fischer-­Tropsch wax, particularly the fraction boiling above 1050°F.
  • Hydrotreating at mild conditions removes impurities in the Fischer-Tropsch wax, but more severe hydrotreating conditions are preferred in the process of the present invention in order to convert some of the higher boiling Fischer-Tropsch wax.
  • This is in contrast, for example, to a petroleum slack wax which normally contains some relatively low melting wax which needs only a slight reduction in pour point to become oil.
  • relatively mild hydrotreating conditions are employed to remove nitrogen and sulfur, while avoiding conversion of the naphthenes and isoparaffins present in the slack wax.
  • Hydrotreater R-1 in order to remove impurities and soften the Fischer-Tropsch wax prior to hydroisomeriza­tion.
  • These conditions include a temperature in the range of about 650°F to 775°F, preferably 700°F to 750°F, a hydrogen pressure between about 500 and 2500 psig (pounds per square inch gauge), preferably between 1000 and 1500 psig, a space velocity of between about 0.1 and 2.0 V/V/Hr (volume of feed/volume of catalyst per hour), preferably 0.2 and 0.5 V/V/Hr, and a hydro­gen gas rate between about 500 and 5000 SCF/B (standard cubic feet of hydrogen per barrel of feed), preferably between 1000 and 2000 SCF/B.
  • the hydrotreating cata­lyst includes the well known hydrotreating catalysts such as Co/Mo or Ni/Mo on alumina.
  • Other hydrotreating catalysts include combination of Co and/or Ni and Mo and/or W on a silica/alumina base.
  • Such hydrotreating catalysts are presulfided, but it is preferred to employ a non-sulfided hydrotreating catalyst in R-1.
  • the hydrotreated Fischer-Tropsch wax from R-1 is introduced into Hydroisomerization Reactor R-2 along with fresh hydrogen or dewatered recycle hydrogen and contacted therein under hydroisomerization conditions with a fluorided Group VIII metal-on alumina catalyst.
  • Hydroisomerization is carried out at tempera­tures ranging between about 500°F and 750°F, preferably from about 600°F to 725°F, at a feed space velocity of from about 0.2 to 2.0 V/V/Hr., preferably from about 0.5 to 1.0 V/V/Hr. Pressure is maintained at from about 500 to 2500 psig, preferably from about 1000 to 1500 psig, and hydrogen is fed into the reactor at a rate of about 500 to 10,000 SCF/B, preferably from about 2000 to 6000 SCF/B.
  • the conditions in hydro­isomerization reactor R-2 are preferably selected to convert about 10 to 35 weight percent (wt.%), preferively 15 to 30 wt% to distillate and lighter (650°F-), of the hydrotreated Fischer-Tropsch wax delivered to R-2. It has been found that such conversion in the 15 to 30 percent range maximizes the production of the desired lubricating oil product.
  • the catalyst employed in hydroisomerization reactor R-2 is a particulate fluorided Group VIII metal-on-alumina catalyst composition where Group VIII refers to the Periodic Table of Elements (E. H. Sargent & Co., Copyright 1964 Dyna-Slide Co.). Platinum is the preferred Group VIII metal.
  • Alumina is the catalyst base and for purposes of this invention alumina includes alumina-containing materials such as silica alumina and the like.
  • the fluorided Group VIII metal-on-alumina catalyst comprises about 0.1 to about 2 percent, preferably from about 0.3 to about 0.6 percent Group VIII metal and from about 2 percent to about 10 percent fluoride, preferably from about 5 percent to about 8 percent fluoride, based on the total weight of the catalyst composition (dry basis), such fluoride concen­tration being herein referred to as the bulk fluoride concentration.
  • the particulate catalyst of the invention will have a fluoride concentration less than about 3.0 weight percent, preferably less than about 1.0 weight percent and most preferably less than 0.5 weight percent at its outer surface layer, provided the surface fluoride concentration is less than the bulk fluoride concentration.
  • the outer surface layer is measured to a depth less than one one hundredth of an inch.
  • the surface fluoride was measured by scanning electron microscope. The remaining fluoride is dis­tributed with the Group VIII metal at a depth below the outer shell into and within the particle interior.
  • the fluoride content of the catalyst can be determined in a number of ways.
  • Fluoride concentration of the sample is determined by ion chromatography analysis of the combustion product solution. Calibration curves are prepared by combusting several concentrations of ethanolic KF standards (in the same manner as the sample) to obtain a 0-10 ppm calibration range. Fluoride concentration of the catalyst is calculated on an ignition-loss-free-basis by comparison of the sample solution response to that of the calibration curve. Ignition loss is determined on a separate sample heated to 800 degrees F for at least 2 hours. Ion chromato­graphic analysis uses standard anion conditions.
  • Fluoride distillation with a titrimetric finish. Fluorides are converted into fluorosilicic acid (H2SiF6) by reaction with quartz in phosphoric acid medium, and distilled as such using super heated steam. This is the Willard-­Winter-Tananaev distillation. It should be noted that the use of super heated, dry (rather than wet) steam is crucial in obtaining accurate results. Using a wet steam generator yielded results 10-20% lower. The collected fluorosilicic acid is tritrated with stan­dardized sodium hydroxide solution. A correction has to be made for the phosphoric acid which is also transferred by the steam. Fluoride data are reported on an ignition-loss-free-basis after determination of ignition loss on sample heated to 400 degree C for 1 hour.
  • the platinum contained on the alumina compo­nent of the catalyst will preferably have an average crystallite size of up to 50 ⁇ , more preferably below about 30 ⁇ .
  • the preferred catalyst of the invention will be relatively free of nitrogen and, accordingly, the catalyst will have a nitrogen/aluminum (N/Al) ratio less than about 0.005, preferably less than about 0.002, and most preferably less than about 0.0015.
  • the catalyst used in the hydroisomerization reactor R-2 will have high intensity peaks characteris­tic of aluminum fluoride hydroxide hydrate as well as the peaks normally associated with gamma alumina.
  • X-ray diffraction data show that the fluoride present in the preferred catalyst will be substantially in the form of aluminum fluoride hydroxide hydrate.
  • This catalyst is described in detail in co-pending application OP-3402 filed in the names of Glen P. Hamner and Willard H. Sawyer.
  • the 5.66 ⁇ peak for the Reference Standard is taken as a value of 100.
  • fluorided platinum-on-alu­mina catalyst having a hydrate level of 60 would therefore have a 5.66 ⁇ peak height equal to 60% of the 5.66 ⁇ peak height of the Reference Standard, with a value of 80 corresponding to a catalyst having a 5.66 ⁇ peak height equal to 80% of the 5.66 ⁇ peak height of the Reference Standard etc.
  • the catalyst used in reactor R-2 will have a hydrate level of at least 60, preferably at least 80, and most preferably at least about 100.
  • the Reference Standard contains 0.6 wt% Pt and 7.2 wt% F on ⁇ alumina having a surface area of about 150 m2/g.
  • the Reference Standard is prepared by treatment of a standard reforming grade platinum on alpha alumina material containing 0.6 wt% Pt on 150 m2/g surface area ⁇ alumina with platinum, followed by single contact with an aqueous solution containing a high concentration of hydrogen fluoride (e.g., 10-15 wt% HF solution such as 11.6 wt% HF solution) with drying at 300°F in accordance with the following procedure.
  • a high concentration of hydrogen fluoride e.g., 10-15 wt% HF solution such as 11.6 wt% HF solution
  • the catalyst employed in R-2 may be prepared in the following manner.
  • the Group VIII metal preferively platinum
  • a preferred method for adding the platinum group metal to the alumina support involves the use of an aqueous solution of a water soluble compound, or salt of platinum to impregnate the alumina support.
  • platinum may be added to the support by co-mingling the uncal­cined alumina with an aqueous solution of chloropla­tinic acid, ammonium chloroplatinate, platinum chlo­ride, or the like, to distribute the platinum substan­tially uniformly throughout the particle.
  • the impregnated support can then be dried and subjected to a high temperature calcination, generally at a temperature in the range from about 700°F to about 1500°F, preferably from about 850°F to about 1300°F, generally by heating for a period of time ranging from about 1 hour to about 20 hours, preferably from about 1 hour to about 5 hours.
  • the platinum component added to the alumina support is calcined at high temperature to fix the platinum thereupon prior to adsorption of a fluoride, suitably hydrogen fluoride or hydrogen fluoride and ammonium fluoride mixtures, into the platinum-alumina composite.
  • a fluoride suitably hydrogen fluoride or hydrogen fluoride and ammonium fluoride mixtures
  • the solution of a water soluble compound, or salt of platinum can be used to impregnate a pre-calcined alumina support, and the platinum-alumina composite again calcined at high temperature after incorporation of the platinum.
  • the Group VIII metal component is substan­tially uniformly distributed throughout a precalcined alumina support by impregnation.
  • the Group VIII metal-­alumina composite is then calcined at high temperature, and the fluoride, preferably hydrogen fluoride, is distributed onto the precalcined Group VIII metal-­alumina composite in a manner that most of the fluoride will be substantially composited at a level below the outer surface of the particles.
  • the catalyst having the fluoride substan­tially in the form of aluminum fluoride hydroxide hydrate is preferably prepared in the following manner.
  • the platinum is distributed, generally substantially uniformly throughout a particulate alumina support and the platinum-alumina composite is calcined.
  • Distribu­tion of the fluoride on the catalyst, preferably hydrogen fluoride is achieved by a single contact of the precalcined platinum-alumina composite with a solu­tion which contains the fluoride in sufficiently high concentration.
  • an aqueous solution contain­ing the fluoride in high concentration is employed, a solution generally containing from about 10 percent to about 20 percent, preferably from about 10 percent to about 15 percent hydrogen fluoride. Solutions contain­ing hydrogen fluoride in these concentrations will be adsorbed to incorporate most of the hydrogen fluoride, at an inner layer below the outer surface of the platinum-alumina particles.
  • the platinum-alumina composite after adsorption thereupon of the fluoride component is heated during preparation to a temperature ranging up to but not exceeding about 650°F, preferably about 500°F, and more preferably 300°F.
  • the catalyst is dried at a temperature ranging up to but not exceeding about 850°F.
  • a characteristic of the inner platinum-fluoride containing layer is that it contains a high concentration of aluminum fluoride hydroxide hydrate. It can be shown by X-ray diffrac­tion data that a platinum-alumina catalyst formed in such manner displays high intensity peaks characteris­tic of both aluminum fluoride hydroxide hydrate and gamma alumina.
  • the isomerate from R-2 may be fractionated and then dewaxed or it may first be introduced with hydrogen into hydrofinishing reactor R-3 containing a hydrogenation catalyst to hydrogenate the unsaturates present in the isomerate product and thereby improve its daylight stability.
  • the reactor conditions are relatively mild and include, for example, a temperature in the range of about 340-450°F, preferably about 356°F to 425°F, at pressures of about 300 to 1500 psi H2, preferably 500 to 1000 psi H2, a gas rate of about 500 to 10,000 SCF/B, preferably 1000 to 5000 SCF/B and a space velocity of about 0.25 to 20 V/V/Hr., preferably about 1-4 V/V/Hr.
  • the catalyst employed in R-3 includes, for example, the hydroisomerization catalyst employed in R-3 or a noble Group VIII metal on a refractory metal oxide such as alumina, silica-alumina and the like.
  • the effluent from R-3 is fractionated in distillation tower F-1 to produce an overhead light end product boiling below 640°F, a lubricating oil fraction boiling in the range of 640°F - 1000°F, preferably in the range of 700°F - 900°F and a residual fraction.
  • the lubricating oil fraction is then introduced into the dewaxing zone D-1 where unconverted wax is removed to result in a lubricating oil having a viscosity index of at least 130, preferably a viscosity index greater than 140, and a pour point no greater than 0°F and prefer­ably a pour point below -6°F.
  • the residual fraction from F-1 will typically have an initial boiling point at atmospheric pressure above 1000°C and will be recycled with the wax from D-1 to the hydroisomeriza­tion reactor R-2.
  • Dewaxing in D-1 is accomplished by techni­ques which permit the recovery of unconverted wax, since, as indicated, this unconverted wax is recycled to the hydroisomerization unit.
  • Solvent dewaxing is utilized in D-1 and employs typical dewaxing solvents.
  • Solvent dewaxing utilizes typical dewaxing solvents such as C3-C6 ketones (e.g. methyl ethyl ketone, methyl isobutyl ketone and mixtures thereof), C6-C10 aromatic hydrocarbons (e.g. toluene) mixtures of ketones and aromatics (e.g.
  • MEK/toluene autorefrigerative sol­vents such as liquified, normally gaseous C3-C4 hydro­carbons such as propane, propylene, butane, butylene and mixtures thereof, etc. at filter temperature of -18°F to -22°F.
  • the isomerate may be dewaxed under miscible conditions with a high yield of dewaxed oil at a high filter rate with a mixture of MEK/MIBK (20/80) used at a temperature in the range -18°F to -22°F. Pour points lower than -6°F can be achieved using lower filter temperatures and other ratios of said solvent but a penalty may be paid due to operation under immis­cible conditions, the penalty being lower filter rates.
  • a synthetic hydrocarbon wax (Fischer-Tropsch source) feed was obtained as a 700°F+ fraction by the distillation of a total Fischer-Tropsch synthesis product.
  • the synthesis wax feed had the following properties: Melting Point, °F >220 Oil Content, wt% nil Sulfur, ppm nil Nitrogen, ppm nil Oxygen, wt% 0.34 Metals (Fe,Co) trace
  • the wax feed was hydroisomerized over a platinum on fluorided alumina catalyst having the following composition: Platinum concentration, wt% 0.58 Platinum Cystallite size ⁇ 26 Fluorine, wt% 7.9 Aluminum Fluoride Hydroxide Hydrate level intensity @5.66 ⁇ (X-ray diffraction) 250 Nitrogen/Al2O3 Atomic Ratio 0.005 Surface area, m2/g 138 Pore volume, cc/g 0.42
  • the catalys was reduced with hydrogen @ 650°F for two hours prior to introducing the 700°F+ wax feed with hydrogen.

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  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Catalysts (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
  • Lubricants (AREA)
EP88311982A 1987-12-18 1988-12-16 Verfahren zur Hydroisomerisierung von Fischer-Tropsch-Wachs zur Herstellung von Schmieröl Expired - Lifetime EP0323092B1 (de)

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US13479787A 1987-12-18 1987-12-18
US134797 1987-12-18

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EP0323092A2 true EP0323092A2 (de) 1989-07-05
EP0323092A3 EP0323092A3 (en) 1989-08-30
EP0323092B1 EP0323092B1 (de) 1992-04-22

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EP (1) EP0323092B1 (de)
JP (1) JPH01301789A (de)
AU (1) AU610671B2 (de)
CA (1) CA1310287C (de)
DE (1) DE3870429D1 (de)
MY (1) MY104076A (de)
NO (1) NO885605L (de)

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EP0743351A3 (de) * 1995-05-19 1997-01-22 Shell Int Research Verfahren zur Herstellung von Basisschmierölen
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US6420618B1 (en) 1998-09-04 2002-07-16 Exxonmobil Research And Engineering Company Premium synthetic lubricant base stock (Law734) having at least 95% noncyclic isoparaffins
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EP1212388A4 (de) * 1999-05-25 2003-05-28 Exxonmobil Res & Eng Co Verfahren zur hydrokonversion von raffinerieprodukten
EP1222239A4 (de) * 1999-05-25 2003-08-27 Exxonmobil Res & Eng Co Hydrokonversion zur herstellung einer schmierölbasis
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WO2004074406A1 (en) * 2003-02-18 2004-09-02 Chevron U.S.A. Inc. Process for producing premium fischer-tropsch diesel and lube base oils
WO2004106467A1 (en) * 2003-05-12 2004-12-09 Chevron U.S.A. Inc. Process for upgrading fischer-tropsch products using dewaxing and hydrofinishing
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CN115709089A (zh) * 2022-11-15 2023-02-24 国家能源集团宁夏煤业有限责任公司 费托合成油加氢精制催化剂及其制备方法和应用

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CA1310287C (en) 1992-11-17
AU610671B2 (en) 1991-05-23
DE3870429D1 (de) 1992-05-27
AU2694588A (en) 1989-06-22
NO885605L (no) 1989-06-19
NO885605D0 (no) 1988-12-16
JPH01301789A (ja) 1989-12-05
EP0323092A3 (en) 1989-08-30
MY104076A (en) 1993-11-30
EP0323092B1 (de) 1992-04-22

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