Classifications

• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
  • B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
  • B01J31/1616—Coordination complexes, e.g. organometallic complexes, immobilised on an inorganic support, e.g. ship-in-a-bottle type catalysts
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
  • B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
  • B01J31/12—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides
  • B01J31/14—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides of aluminium or boron
  • B01J31/143—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides of aluminium or boron of aluminium
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
  • B01J2531/80—Complexes comprising metals of Group VIII as the central metal
  • B01J2531/84—Metals of the iron group
  • B01J2531/842—Iron
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
  • B01J2531/80—Complexes comprising metals of Group VIII as the central metal
  • B01J2531/84—Metals of the iron group
  • B01J2531/845—Cobalt
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
  • B01J2531/80—Complexes comprising metals of Group VIII as the central metal
  • B01J2531/84—Metals of the iron group
  • B01J2531/847—Nickel
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
  • B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
  • B01J31/22—Organic complexes
  • B01J31/2204—Organic complexes the ligands containing oxygen or sulfur as complexing atoms
  • B01J31/2208—Oxygen, e.g. acetylacetonates
  • B01J31/2226—Anionic ligands, i.e. the overall ligand carries at least one formal negative charge
  • B01J31/223—At least two oxygen atoms present in one at least bidentate or bridging ligand
  • B01J31/2234—Beta-dicarbonyl ligands, e.g. acetylacetonates
• • 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
  • 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
  • C10G2400/14—White oil, eating oil

Definitions

• Raw distillates and semi-refined oils of suitable boiling range and viscosity are refined, or further refined, in a hydrogenation process, at suitable conditions, in the presence of a catalyst which comprises a support and a transition metal complexed with an organometallic compound, to yield colorless mineral oils, i.e., white oils.
• a catalyst which comprises a support and a transition metal complexed with an organometallic compound, to yield colorless mineral oils, i.e., white oils.
• These highly refined oils are used in pharmaceuticals and cosmetics and similar compositions requiring oil components that meet certain high quality standards.
• White oils are highly refined oils derived from petroleum which have been extensively treated to virtually eliminate oxygen, nitrogen, sulfur compounds and reactive hydrocarbons such as aromatic hydrocarbons. White oils fall into two classes, i.e., technical white oils which are used in cosmetics, textile lubrication, insecticide base oils, etc., and the even more highly refined pharmaceutical white oils which are used in drug compositions, foods and for the lubrication of food handling machinery. For all of these applications white oils must be chemically inert and without color, odor and taste.
• the conventional method of making white oils involves refining petroleum oils with sulfuric acid.
• the acid removes impurities and reactive compounds by chemical reaction and by solvation.
• Acid treating is costly because it results in low product yields and produces large amounts of sludge and spent acid which must be disposed of, along with spent clay used for treatment of the product to remove traces of sulfonates and the like.
• White oil specifications are rather difficult to meet, for such oils must have a color of +30 Saybolt, must pass the UV Absorption Test (ASTM D-2008) and the USP Hot Acid Test (ASTM D-565 Nonetheless, it is a primary objective of the present invention to obviate these and other prior art difficulties and, in particular, to provide a new and improved process, or process combination, for manufacture of white oils which will eliminate any necessity of acid treating.
• a further object is to provide a process for manufacturing highly stable white oils from raw distillates and semi-refined oils in good yield containing very insignificant concentrations, if any, of sulfur, nitrogen, oxygen and aromatics.
• a specific object is to provide a process combination including a sequence of steps for manufacturing semi-refined oils, and subsequent treatment of such oils in the presence of highly active complex catalysts, at suitable conditions, for essentially complete saturation of the aromatics to produce white oils in good yield.
• the present invention provides a process comprising treating petroleum oils of suitable boiling range and viscosity, including raw distillates and semi-refined oils, and refining the latter to white oil specifications by hydrogenation with highly active supported transition metal complex catalysts, at hydrogenation conditions.
• the catalyst complex is formed by depositing a transition metal salt from solution on a suitable support material and activating the salt with a liquid-soluble organo-metallic compound.
• Raw distillates and semi-refined oils of suitable boiling range and viscosity provide feedstocks suitable for use in the preparation of white oils by contact with the highly active complex catalysts, at hydrogenation conditions.
• the feedstocks can be obtained by conventional processing comprising (a) solvent extracting a lubricating oil or raw distillate to obtain a rafi'mate; (b) treating the raffinate with hydrogen over an active hydrodesulfurization catalyst at conditions suitable to reduce the sulfur content, and then (c) distilling the hydrotreated product under vacuum to remove overhead a low boiling fraction, while recovering a higher boiling, semirefined low sulfur oil fraction.
• a petroleum oil obtained by distillation, boiling in the range of 400 to l,025 F.
• raffinate boiling in the range of about 400 to l,025 F.
• the raffinate can be hydrogenated, if desired, or necessary, with a conventional hydrodesulfurization catalyst to produce a low sulfur oil containing, preferably, less than about 5 ppm sulfur.
• This oil, or feedstock can then be upgraded to specification white oil by a second hydrogenation in the presence of a highly active catalyst complex formed bya supported transition metal salt, activated with a liquid-soluble organo-metallic compound.
• Suitable feedstocks for conversion to white oils over the highly active complex catalysts are those boiling within'a range of from about 400 to l,025 F., a higher, preferably from about 650 F. to l,025 F. While higher boiling feedstocks can be used, this is not generally desirable inasmuch as process conditions must be increased in severity to an impractical extent. Viscosities range preferably from about 30 to about 2,500 SSU at F., and more preferably from about 35 to 500 SSU at 100 F., but viscosity can be readily controlled, e.g., by topping.
• aromatics content of the initially treated feed is not critical inasmuch as aromatics can be reduced to an acceptable level by extraction and prehydrogenation, but the aromatics content of the feedstock directly used for treatment and hydrogenation with the complex catalyst should preferably be no greater than about 5 percent, based on the weight of the feedstock, and is more preferably less.
• Conventional solvent extraction processes can be used to reduce the aromatic hydrocarbon content of the oil.
• a preferred extraction with phenol at a temperature in the range of 100 to 300 F. and a pressure in the range of about ambient to l00 psig provides a suitable means of aromatics removal.
• a pressure in the range of about ambient to l00 psig provides a suitable means of aromatics removal.
• the raffinate is hydrogenated at relatively severe conditions to remove theheterocyclic compounds, and in particular to reduce the sulfur content of the oil, preferably to less than about 5 ppm sulfur.
• Suitable hydrogenation conditions include temperatures in the range of about 400 to 800 F., and preferably in the range of about 600 to 700 F.; pressures in the range of about l,000 to 10,000 and preferably in the range of about 500 to 5,000 psig; space velocities in the range'of about 0.1 to 10 VIl-lrJV, preferably in the range of about 0.1 to 2 V/Hr./V; and hydrogen rates of from about 500 to 10,000 SCF/Bbl. and preferably hydrogen rates of about l,000 to 5,000 SCF/Bbl. of feed.
• Suitable hydrotreating catalysts comprise one or more hydrogenation metals supported on a suitable carrier material.
• the metals are in the form of metal oxides or metal sulfides. Salts of Group VI and Group VIII metals are the preferred hydrogenating components.
• oxides or sulfides of molybdenum, tungsten, cobalt, nickel and iron are used.
• Alumina, alumina containing 1 to 10 weight percent silica, bauxite, kieselguhr, etc., are preferred support materials.
• the most preferred catalysts are sulfided cobalt molybdate or sulfided nickel molybdate on alumina or silica alumina.
• the catalyst can be disposed for contacting in a fixed bed for liquid phase or mixed phase contacting.
• This first stage of hydrogenation performs several functions, including hydrodesulfurization, hydrodenitrogenation, saturation of olefins, some saturation of aromatic hydrocarbon rings, etc.
• the hydrofined, or semi-refined, oils can be topped, if desired, to adjust viscosity and specific gravity in accordance with market requirements.
• the feedstocks, or white oil base stocks can be hydrogenated in the presence of the high activity complex catalysts to produce white oils.
• Pressures, space velocities and hydrogen rates are essentially the same as in the first hydrogenation stage wherein salts of Groups VIB and VIII hydrogenation metals are employed,,though temperatures are generally lower.
• the temperature employed in hydrogenation of the feedstocks with the highly active complex catalysts ranges from about 350 to 600 F., and more preferably from about 475 to 525 F.
• the highly active complex catalysts are prepared by the steps of impregnating a support with a solution of a liquid soluble compound of a transition metal, preferably a Group VIII metal of the Periodic Chart of the Elements; and then activating the supported metal species with a solution of an organo-metallic compound, a metallic constituent of which is selected from Groups I, II and III of the Periodic Chart of the elements.
• a transition metal preferably a Group VIII metal of the Periodic Chart of the Elements
• an organo-metallic compound a metallic constituent of which is selected from Groups I, II and III of the Periodic Chart of the elements.
• the transition or Group VIII metal salt can be dissolved in an aqueous or nonaqueous medium to form the solution, depending on the specificnature and characterof the salt.
• a watersoluble fonn of salt is used, and in impregnation of the support, subsequent activation steps include: heat-treating the impregnated support sufficient to form a complex of a species of the metal at the surface of the support and to remove liquid and adsorbed oxygen; activating the supported metal complex by contacting same with a liquid soluble organo-metallic compound, a metallic constituent of which is selected from Groups I, ll and Ill of the Periodic Chart of the Elements, and treating the activated supported metal complex to eliminate volatile matter.
• a highly te naceous chemical bonding can be formed between the surface of certain types of supports and transition or Group VIII metals, particularly iron, cobalt and nickel, of the Periodic Chart of the Elements, when the latter are applied to the supports as solutions of the desired metal, and heat treated.
• the supported species, or product formed by the heat treatment is further chemically altered and activated by treatment with liquid soluble organometallic compounds, wherein the metal constituent of the compound is selected from Groups I, II and III of the Periodic Chart of the Elements.
• a support is first impregnated with a solvent-soluble or water-soluble species of a transition or Group VIII metal salt, preferably iron, cobalt, and nickel, by contact or immersion of the support in an organic or aqueous solution of a salt of the desired metal.
• a solvent-soluble or water-soluble species of a transition or Group VIII metal salt preferably iron, cobalt, and nickel
• the support is impregnated with from about 1 to about 20 percent metal, and preferably from about 2 to about l percent metal, based on the total weight of the deposited metal and support.
• Exemplary of water-soluble salts useful for application of the desired metals are halides, e.g., ferric chloride, ferrous chloride, cobaltous chloride, nickel chloride, nickel bromide, nickel fluoride, sulfates, e.g., ferric sulfate, ferrous ammonium sulfate, nickel sulfate, cobaltous sulfate, nitrates, e.g., cobaltous nitrate, nickel nitrate, ferric nitrate, water-soluble carboxylic acid salts, e.g., cobaltous acetate, nickel acetate, ferric or ferrous acetates, formates, propionates, and water-soluble phosphates and the like.
• halides e.g., ferric chloride, ferrous chloride, cobaltous chloride, nickel chloride, nickel bromide, nickel fluoride, sulfates, e.g., ferr
• Exemplary of salts useful for application by solution in organic solvents are the acetyl acetonates, carbonates, halides, chelates, and various heterocyclic compounds of iron, cobalt and nickel.
• the support in powder or granular form, is impregnated with an aqueous salt solution it is next treated by establishing time-temperature relationships suitable to produce a chemical change on the surface of the support and to remove water and adsorbed oxygen.
• the impregnated support can be heated in air, in inert atmosphere or in vacuum, e.g., 20 to 29 inches of mercury, at from about 300 to about l,200 F., or preferably from about 400 to about 800 F., for periods ranging from about 0.5 to about 4 hours, or preferably from about 1 to about 2 hours.
• the reaction between the salt and support can be accomplished by the elevated temperatures while moisture is stripped from the support with nitrogen, or other nonreactive gas.
• the impregnation and heat-treating steps can be conducted in multiple stages.
• the support can be impregnated and thence dried, or partially dried, at low temperature.
• the support can thence be reimpregnated and again dried, or partially dried.
• the heat treatment per so can also be conducted in multiple stages, if desired.
• the impregnated support, to facilitate handling can thus be subjected to a first rather mild heat treatment to dry the support and thence, in a second step, to a more severe treatment to produce the desired chemical change at the surface.
• supported catalysts such as supplied by commercial catalyst manufacturers, e.g., iron, cobaltor nickel, alone or in combination with other metals such as molybdenum, tungsten or the like, are also amenable to such treatments to transfonn them into highly active catalysts.
• Suitable supports are the oxides of Group II, III, IV, V and VIB of the Periodic Chart of the Elements, though the oxides of Groups II, IIIA and IVB are preferred.
• the Group lllA metal oxides, particularly boria and alumina, are especially preferred.
• Alumina supports in fact, are quite outstanding from a cost-effectiveness standpoint and are readily available. Silica-free alumina has been found especially suitable though silica alumina combinations of types used for cracking catalysts are also highly active.
• Group II metal oxides such as zinc oxide, magnesium oxide, calcium oxide, strontium oxide and barium oxide and also the Group IV metal oxides, e.g., titanium oxide and zirconium oxide, Group V metal oxides, e.g., vanadium oxide, and activated carbon and coke are effective.
• Certain natural clays, diatomaceous earths, e.g., kieselguhr, and other supports are also useful.
• the impregnated support is activated by treatment with an organo-metallic compound, suitably a hydrocarbon solution of an organo-metallic compound, ametallic constituent of which is selected from Group I, II and III, or more preferably from Group IA, IIB, and 111A of atomic number ranging from 3 to 30, of the Periodic Chart of the Elements.
• an organo-metallic compound suitably a hydrocarbon solution of an organo-metallic compound, ametallic constituent of which is selected from Group I, II and III, or more preferably from Group IA, IIB, and 111A of atomic number ranging from 3 to 30, of the Periodic Chart of the Elements.
• compounds include those having the formula: M(R,,)X wherein M is a Group I, II, or III, and preferably a Group IA, 118 or "M, metal having an atomic number of from 3 to 30, R is hydrogen or a monovalent organo or hydrocarbon radical, preferably ethyl,'propyl, isopropyl, butyl, isobutyl, cyclopentyl, cyclohexyl, phenyl, naphthyl, and benzyl; X is selected from the group consisting of halogen, R, where R is a hydrocarbon radical as previously described for R, and OR,; and n is an integer ranging from 1 to 2.
• the R (and R groups can be the same or different, substituted or unsubstituted, saturated or unsaturated, and can be alkyl, aryl, alkaryl, aralkyl, or cycloalkyl.
• Such groups include, for example, methyl, ethyl, n-propyl, isopropyl, isobutyl, sec-butyl, tert-butyl, n-amyl, isoamyl, heptyl, n-octyl, n-dodecyl, and the like; 2-butenyl, 2-methyl-2-butenyl and the like; cyclopentyl-methyl, cyclohexylethyl, cyclohexylpropyl and the like; 2-phenylethyl, Z-phenylpropyl, Z-naphthylethyl, methyl naphthylethyl and the like; cyclopentyl,
• Preferred activating agents are the AIR, or tri-alkyl substituted products of aluminum, particularly those containing alkyl groups having from one to about 12 carbon atoms, and more particularly those containing from one to about four carbon atoms, especially linear alkyl groups.
• Exemplary of such compounds, which contain up to about 36 carbon atoms in the molecule, are trimethyl aluminum, triethyl aluminum, tri-nbutyl aluminum, tri-n-hexyl aluminum, tridodecyl aluminum and the like. 7
• the activation can be carried out with pure or diluted metal alkyl compounds in liquid or in the vapor phase.
• Hydrocarbon diluents of the parafiinic, cycloparafiinic or aromatic types are entirely suitable and the metal alkyl compound may be present in concentrations of 5 percent to 50 percent in the diluent.
• a solution of about 20 percent aluminum triethyl in a paraffinic diluent is a preferred activation system.
• the activation reaction is quite exothermic and it may be desirable to remove the heat of activation.
• the temperature during the activation step is maintained in the range of from about 60 to about 500 F., preferably from about 100 to about 200 F.
• the molar ratio of complexing agent (in terms of, e.g., the aluminum to the transition or Group VIII metal) ranges from about 1:1 to about :1.
• Considerable gas liberation occurs during activation and these gases are normally vented from the system. The activation is allowed to proceed until reaction is no longer observed, generally 0.5 hour to 2 hours in contact with at least some excess of metal alkyl compound.
• the excess liquid can be drained from the catalyst, if desired.
• This can be done by any suitable method such as by washing, drying or the like, but preferably the activated catalyst is subjected to heattreatment at temperatures sufficient to thoroughly dry and condition the catalyst.
• a heat treatment is necessary for activation.
• the heat treatment is conducted in a nonreactive or hydrogen atmosphere at temperatures ranging from about 250 to about 800 F., and more preferably from about 200 to about 500 F., for periods ranging up to 24 hours, and preferably from about 0.5 to about 4 hours, or more preferably from about 1 to about 2 hours.
• Complete or partial vacuum may also be used to aid in removal of excess solvent and organo-metallic alkyl compounds.
• the exact nature of the complex formed in the activation step is not known, but it is believed that this step produces a metal-to-metal bond between the metal species of the salt and the metal species of which the support is formed.
• this step produces a metal-to-metal bond between the metal species of the salt and the metal species of which the support is formed.
• the nickel becomes bonded to active sites on the support, probably to aluminum.
• the transition or Group VIII metal species therefore, becomes highly dispersed in atomic form rather than in bulk crystallite form as in conventional catalysts, producing a highly active and stable hydrogenation catalyst.
• EXAMPLE 1 Approximately 39 g. of nickel acetylacetonate is dissolved in 350 cc. of hot toluene. 75 g. of 12-20 mesh activated alumina is added to the solution. The solvent is evaporated by heating. 86.5 cc. of triisobutyl aluminum in 260 cc. of n-heptane is added to the nickel impregnated support. The aluminum-to-nickel atomic ratio is 2.511. The nickel complex is heated in a hydrogen stream at 600 F. to remove the solvent and yield a catalyst containing about 10 weight percent nickel.
• EXAMPLE 2 The catalysts of Examples 1 and 2 are tested comparatively in the same reactor.
• the feedstocks, or white oil base stocks, are nonsolvent extracted naphthenic lubricating oil distillates previously hydrodesulfurized at 700 F. and 1500 psigin the presence of cobalt molybdate catalyst to reduce the sulfur content of the oil to less than 2 parts per million.
• the conditions for the hydrofinishing treatment are 500 F., 2000 psig, 0.25 V/Hr./V and 3,000 SCF/Bbl. hydrogen.
• Table I thus shows the results obtained with the two catalysts for a low viscosity feedstock (Feed A, having a viscosity at F. of 75 SSU).
• the rather insensitive test with silica gel chromatography shows that the products from hydrogenation with both catalysts contains essentially no aromatics.
• a Tia Juana heavy grade distillate (850-l,050 F; 60.6-71.9 percent yield on crude) is prepared, and phenol-extracted to produce a raftinate in 40-45 percent yield, based on the weight of the distillate.
• the rafiinate is hydrodesulfurized over a 5/ 25 cobalt molybdate catalyst at 1,500 psig, 700 F. and 0.25 V/V/Hr. and then topped to 800 F at 80. percent yield, to provide a semirefined oil.
• EXAMPLES 4-6 A Tia Juana light grade oil, 675-800 F. distillate, 45 l-52.4 percent, based on the weight of crude, is phenol-extracted and subjected to hydrodesulfurization as in the foregoing example, and then topped to 600 F., at 95 percent yield. This feedstock, or white oil base stock, is then hydrogenated with aluminum alkyl reduced metal catalysts at 2,000 psig, 500 F. and 0.36 LHSV prepared as follows: 7
• Viscosity at 100 F. SSU 478 450 439 462 453 Color, Saybolt +29 +24 +28 Aromatics, weight percent 28. l 1. 6 Nil 11. 4 5. 3 UV Absorption 270-278 mp, 1./g.
• the semirefined oil is then hydrogenated at 2,000 psig, 500 F 0.25 V/V/l-lr., and 2,000 SCF/Bbl. first over the commercial catalyst as defined in Example 2, and then over the alkyl activated catalyst defined in Example 1. The results are tabulated in Table lll.
• catalyst freed of excess liquid by placing on absorbent paper towels. The catalyst is dried for 3 hours in a vacuum oven at 475550 F. The recovered catalyst weighs l07.4 grams, and analyzes 5.3 percent iron (calculated as Fe).
• a heated quartz reaction tube is charged with 25.7 grams of the above catalyst and a preheat area above the catalyst bed is filled with stainless steel distillation packing.
• the catalyst is heated in a stream of dry nitrogen at a temperature of 500-55 0 F. for one hour and is then cooled in nitrogen to room temperature.
• the reactor is flooded from the bottom with a 20 percent solution of aluminum triethyl. Considerable gas is evolved and the maximum temperature reached is 200 F. After 1.33 hours, the solution is withdrawn. A rapid flow of nitrogen is introduced and the temperature is increased to 350 F. Stripping is continued for about 30 minutes.
• a commercial cobalt molybdena-on-alumina catalyst (Nalco 471A) containing about 3.5 percent C00 and 12 percent MoO and in the form of l/16-inch extruded rods calcined at l,200 F. for 12 hours and then charged (36.7 grams) to the quartz reaction tube is heated in a flow of dry nitrogen. After cooling in dry nitrogen, the catalyst bed is flooded with 20 percent aluminum triethyl. Maximum temperature reached is F. After 40 minutes, the solution is withdrawn and the catalyst brought to 600 F. in a stream of dry hydrogen. Substantially all volatile material is removed in 15 minutes at 500 F.
• the quartz tube is charged with 48.2 gms. of the above catalyst and the catalyst is heated in a stream of dry nitrogen at 600 F. for l hour. After cooling to room temperature, the catalyst is treated with 20 percent AlEt (heptane) solution for a period of 90 minutes during which the maximum temperature noted is 215 F.
• the catalyst After draining off the liquid, the catalyst is treated in a flow of dry hydrogen at 400 F. for 1 hour.
• a process for producing a white oil comprising contacting a low sulfur content white oil base stock boiling within a range of from about 400 to about l,025 F. and having a viscosity ranging from about 35 to about 2,500 SSU at 100 F. at hydrogenation conditions with hydrogen and a catalyst comprising a complex of a metal selected from the group consisting of iron, cobalt and nickel composited with a support selected from the group consisting of alumina, silica-alumina and boria, said catalyst having been prepared by reacting a composite of a salt of the said metal and said support with an aluminum compound having the general formula AlR in which R is an alkyl, aryl, alkaryl, aralkyl or cycloalkyl radical and heating in a non-reactive atmosphere to activate the said catalyst.
• a process for producing white oil from a petroleum lubricating oil fraction containing contaminants including aromatic hydrocarbons, sulfur compounds nitrogen compounds comprising the steps of:
• a process for producing a white oil consisting essentially of the steps of:
• step (c) comprises a sulfided cobalt molybdate on alumina.
• topped semi-refined white oil is one having a viscosity ranging from about 30 to about 500 SSU at 100 F.
• a process for processing white oil comprising forming a white oil base stock by at extracting an oil boiling in a range of from about 400 to about l,025 F., and having a viscosity of about 35 to about 2,500 SSU atl00 F. with a solvent to produce a raffinate of reduced aromatic content, said raft'mate boiling within the range of from about 400 to about 1,025" F.,
• hydrodesulfurizing the raffinate by contact with a hydrogenation catalyst comprising a support material and a hydrogenation component selected from the group consisting of Group Vl-B metals, Group VIII metals and mixtures thereof, at a temperature ranging from about 400 to 800 F., a pressure ranging from about 1,000 to 10,000 psig, space velocities ranging from about 0.1 to 10 Vll-lr./V, and at hydrogen rates of from about 500 to 10,000 SCF/Bbl contacting said desulfurized oil at hydrogenation conditions with hydrogen and a catalyst composite comprising support selected from the group consisting of alumina, silicaalumina and boria, and a metal selected from the group consisting of iron, cobalt and nickel, said catalyst composite having been prepared by reacting the said composite with an aluminum compound having the general formula AIR in which R is an alkyl, aryl, alkaryl, aralkyl or cycloalkyl radical and recovering a colorless white oil containing essentially no aromatic compounds.

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• 1969
  • 1969-10-28 US US871943A patent/US3658692A/en not_active Expired - Lifetime
• 1970
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• 1972
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