Classifications

• • 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
  • C10G45/44—Hydrogenation of the aromatic hydrocarbons
  • C10G45/46—Hydrogenation of the aromatic hydrocarbons characterised by the catalyst used
  • C10G45/48—Hydrogenation of the aromatic hydrocarbons characterised by the catalyst used containing nickel or cobalt metal, or compounds thereof
  • C10G45/50—Hydrogenation of the aromatic hydrocarbons characterised by the catalyst used containing nickel or cobalt metal, or compounds thereof in combination with chromium, molybdenum or tungsten metal, 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
  • C10G2400/00—Products obtained by processes covered by groups C10G9/00 - C10G69/14
  • C10G2400/10—Lubricating oil

Definitions

• This invention relates to the manufacture of high grade viscous oil products from crude petroleum fractions. It is particularly directed to the manufacture of very high quality lube base stock oils from crude stocks of high wax content, commonly classified as “wax base” in contrast to “naphthenic base” crudes.
• wax base crude stocks of high wax content
• naphthenic base crudes.
• the latter crudes are relatively lean in straight chain paraffins and yield viscous fractions which inherently possess low pour points.
• Lube base stock oils are conventionally prepared by refining distillate fractions or the residuum prepared by vacuum distilling a suitable crude oil from which the lighter portion has been removed by distillation in an atmospheric tower.
• the charge to the vacuum tower is commonly referred to as an atmospheric resid or reduced crude, and the residuum from the vacuum tower is distinguished from the starting material by referring to it as the vacuum resid.
• the vacuum distillate fractions are upgraded by a sequence of unit operations, the first of which is solvent extraction with a solvent selective for aromatic hydrocarbons. This step serves to remove aromatic hydrocarbons of low viscosity index and provides a raffinate of improved viscosity index and quality.
• Various processes have been used in this extraction stage employing solvents such as furfural, phenol, sulfur dioxide, and others.
• the vacuum resid because it contains most of the asphaltenes of the crude oil, is conventionally treated to remove these asphalt-like constituents prior to solvent extraction to increase the viscosity index.
• the raffinate from the solvent extraction step contains paraffins which adversely affect the pour point.
• the waxy raffinate regardless of whether prepared from a distillate fraction or from a vacuum resid, must be dewaxed.
• Various dewaxing procedures have been used and the art has gone in the direction of treatment with a solvent such as methyl ethyl ketone (MEK)/toluene mixtures and/or catalytic dewaxing to remove the wax and provide a dewaxed oil.
• MEK methyl ethyl ketone
• the dewaxed raffinate may then be finished by any of a number of sorption or catalytic processes to improve color and oxidation stability, e.g., clay percolation or hydrofinishing.
• the quality of the lube base stock oil prepared by the sequence of operations outlined above depends on the particular crude chosen as well as the severity of treatment for each of the treatment stages. Additionally, the yield of a high quality lube base stock oil also depends on these factors and, as a rule, the higher the quality sought, the less the yield. In general, naphthenic crudes are favored because less loss is encountered, particularly in the dewaxing step. In many cases, however, waxy crudes are more readily available, and it would be desirable to provide a process for preparing very high quality lube base stock oils in good yields from such waxy crude oils.
• U.S. Patent No. 4,437,975 describes a process for preparing a lube base stock oil from a vacuum resid by catalytically dewaxing the vacuum resid over a zeolite catalyst such as ZSM-5 and cascading the entire effluent, including hydrogen, into a hydrotreating reactor operated under relatively mild conditions, i.e., at a temperature from 260° to 357 ° C (500 ° to 675°F) and at a hydrogen partial pressure at the reactor inlet of 1034 to 10340 kPa.a (150 to 1500 psia).
• the olefins present in the dewaxed feedstock are substantially hydrogenated thereby eliminating a principal source of oxidative and thermal instability.
• These hydrotreating conditions are not severe enough, however, to effect any appreciable reduction in the content of aromatic compounds and nitrogen- and sulfur-containing compounds the presence of which limits the use of the resulting oils to relatively undemanding service applications.
• U.S. Patent No. 3,959,122 describes a process for producing a technical white oil having an ultraviolet absorptivity in the 280 to 289 millimicron region of less than 2.0 and having a viscosity in the range of 300 to 600 SUS (Saybolt Universal Seconds) at 38 ° C (100 ° F) in which a paraffinic distillate having a viscosity in the range of 400 to 600 SUS is hydrorefined at a temperature of 288 ° to 316 ° C (550 ° to 600 ° F), at a hydrogen partial pressure in the range of 5520 to 20685 kPa (600 to 3000 psi) and a total pressure in the range of 5520 to 41400 kPa g (800 to 6000 psig) in the presence of a sulfided nickel/molybdenum hydrogenation catalyst and at a liquid hourly space velocity (LHSV) of 0.1 to 1.0. Under these hydrorefining conditions, a significant
• British Published Patent Application No. 2059433A describes the preparation of lubricating oil basestocks by subjecting a petroleum vacuum distillate fraction or residue to a process including solvent extraction followed by mild catalystic hydrogenation at 310-450 ° C over a sulfided hydrogenation catalyst containing oxides of molybdenum and nickel or cobalt followed by dewaxing.
• This invention provides a process for preparing a very high quality lube base stock oil having excellent thermal and oxidation stability from a waxy crude oil.
• the process comprises:
• a sulfided cobalt/molybdenum catalyst provides several advantages over a sulfided nickel/molybdenum catalyst as used in the hydrorefining process of U.S. Patent No. 3,959,122 referred to above.
• the greater stability of a cobalt/molybdenum catalyst compared to that of a nickel/molybdenum catalyst permits the former to be regenerated at a higher temperature and correspondingly shorter period of time than the latter thereby reducing reactor down-time and increasing productivity.
• the greater stability of the cobalt/molybdenum catalyst makes it more suitable for steam/air regeneration which is less expensive than the nitrogen/air regeneration methods more commonly employed with nickel/molybdenum catalysts.
• cobalt/molybdenum is significantly easier to sulfide/presulfide, the form in which the catalyst must be used in the hydrotreating process herein.
• Known unit processes are applied to distillate or vacuum resid fractions of waxy crude in particular sequence and within limits to prepare lube base stock oils used, for example, in hydraulic fluids, motor oils, turbine oils, marine oils and gear lubricants.
• the first step after preparation of a distillate fraction of suitable boiling range is extraction with a solvent which is selective for aromatic hydrocarbons, e.g., furfural, phenol, n-methylpyrrolidone, or others, to remove undesirable components of the fraction.
• a vacuum resid fraction it is required to propane deasphalt the resid prior to solvent extraction. In some instances, such as with a cylinder stock, solvent extraction of the deasphalted vacuum resid can be omitted.
• the raffinate from solvent extraction or propane deasphalting of vacuum resid is then dewaxed in a conventional manner, e.g., by treatment with a solvent such as MEK/toluene, propane or catalytically in the presence of hydrogen over a catalyst of an aluminosilicate zeolite having a silica to alumina ratio greater than 12 and a constraint index of 1 to 12 or by a combination of solvent and catalytic dewaxing as in U.S. Patent No. 3,755,138.
• the dewaxed oil is then hydrotreated in a single stage hydrotreating unit in the presence of sulfided cobalt/molybdenum catalyst operated under the foregoing specified conditions to provide a white oil possessing substantially improved color, demulsibility and oxidation stability and ideally suited for severe service applications such as turbine oils.
• the hydrotreated product is thereafter distilled, i.e., topped by distillation, to separate low boiling products of dewaxing in order to meet physical property specifications such as flash point and others.
• Conducting the unit processes at the conditions more fully specified hereinafter imparts high quality characteristics to the lube base stock oils and at the same time produces high yields of finished oils.
• the wax base crudes (sometimes called “paraffin base") from which the charge stock is derived by distillation constitute a well recognized class of crude petroleums.
• Many scales have been devised for classification of crude, some of which are described in Chapter VII Evaluation of Oil Stocks of "Petroleum Refinery Engineering", W.L. Nelson, McGraw-Hill, 1941.
• a convenient scale identified by Nelson at page 69 involves determination of the cloud point of the Bureau of Mines "Key Fraction No. 2" which boils between 275 ° and 300 ° C (527 ° and 572 ° F) at 5330 kPa (40 mm) pressure. If the cloud point of this fraction is above -15 ° C (5 ° F), the crude is considered to be a wax base.
• Known and conventional solvent extraction by counter current extraction with at least an equal volume (100 vol. %) of a selective solvent such a furfural is contemplated. It is preferred to use from 1.5 to 4.0 volumes of solvent per volume of oil.
• the furfural raffinate product is thereafter subjected to any one of several known and conventional solvent and/or catalytic dewaxing procedures.
• Solvent dewaxing is a well known technique and needs no detailed description here.
• the raffinate from the solvent refining unit is combined with a selective solvent and chilled to the appropriate temperature to crystallize the wax which is then separated therefrom.
• suitable solvents are (a) the aliphatic ketones having from 3 to 6 carbon atoms such as acetone, methyl ethyl ketone (MEK) and methyl isobutyl ketone (MIBK) and (b) propane, butane, and propylene as well as mixtures of the foregoing ketones and mixtures of the aforesaid ketones with aromatic compounds such as benzene and toluene.
• halogenated low molecular weight hydrocarbons such as the C 2 -C 4 chlorinated hydrocarbons, e.g., dichloromethane and dichloroethane and mixtures thereof, can be used as solvents.
• suitable solvent mixtures are methyl ethyl ketone and methyl isobutyl ketone, methyl ethyl ketone and toluene, dichloromethane and dichloroethane and propylene and acetone.
• the raffinate is dewaxed by the selected solvent or solvent mixture which is adjusted to the composition of the charge stock to meet specifications for the particular lube base stock and the contemplated end-use, such being determined in accordance with well established practices.
• the waxy raffinate from the solvent extraction operation is mixed with hydrogen and contacted at 260 ° to 375 ° C (500 ° to 675°F) with a catalyst containing a zeolite ZSM-5 or other aluminosilicate zeolite having a silicate/alumina ratio above 12 and a constraint index of 1 to 12, with or without a hydrogenation component, and at an LHSV of 0.1 to 2.0 volumes of charge oil volume of catalyst per hour.
• the preferred space velocity is 0.5 to 1.0 LHSV.
• the higher melting point waxes so removed are those of higher market value than the waxes removed in conventionally taking the product to a still lower pour point below -12 ° C (10 ° F).
• cracked (and hydrogenated) fragments from cracking wax molecules in the catalytic dewaxer will have adverse effects on the flash point of the dewaxed raffinate product and are therefore removed by distillation of the product to flash point specifications.
• effluent from the solvent or catalytic dewaxing step is introduced into a conventional fixed bed single stage hydrotreating reactor containing a sulfided cobalt/molybdenum catalyst on a support, e.g., one of alumina.
• a sulfided cobalt/molybdenum catalyst on a support, e.g., one of alumina.
• Such catalysts are well known in the art and are commercially available.
• Shell's S 344 catalyst, a 1.6 mm (1/16 inch) pelletized extrudate of sulfided cobalt (2.4 wt. %) and molybdenum (9.8 wt. %) on alumina having a surface area of 190 m 2 /gm and a pore volume of 0.56 cc/gm has been found to provide entirely acceptable results.
• the hydrotreating reactor is operated at an average reactor bed temperature from 316 ° to 357 ° C, a hydrogen partial pressure from 13800 to 17240 kPa.a, at the reactor outlet, an LHSV from 0.3 to 0.6, and a hydrogen circulation rate from 53.4 to 445 vol/vol (300 to 2500 SCF per barrel).
• the effluent from the hydrotreating reactor is steam-stripped to remove the most volatile components and thereby meet flash point and other product specifications.
• the lube base stock oil product in each of the four cases was a technical grade white oil of very high quality which is well suited for use as a turbine oil.
• This example illustrates the process of the present invention employing the reactor and catalyst of Example 1 but employing as the charge stock, a catalytically dewaxed solvent-extracted distillate of 200 SUS at 38 ° C (100 ° F) derived from a Mexican crude (Isthmus).
• the conditions of hydrotreatment, the properties of the charge stock and the properties of the hydrotreated oil are set forth in Table 3 as follows:
• the hydrotreated oil was of technical white oil grade and is well suited for use as a turbine oil.

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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)
• Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
• Catalysts (AREA)

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• 1986
  • 1986-06-13 AU AU58719/86A patent/AU592347B2/en not_active Ceased
  • 1986-06-23 ES ES556430A patent/ES8800710A1/es not_active Expired
  • 1986-06-26 CA CA000512563A patent/CA1280989C/en not_active Expired - Lifetime
  • 1986-07-01 DE DE8686305095T patent/DE3674326D1/de not_active Expired - Fee Related
  • 1986-07-01 EP EP19860305095 patent/EP0219927B1/en not_active Expired
  • 1986-07-03 JP JP61155217A patent/JPS6215289A/ja active Pending
  • 1986-07-04 BR BR8603144A patent/BR8603144A/pt not_active IP Right Cessation

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