AU2001234852A1 - Functional fluid - Google Patents

Functional fluid

Info

Publication number
AU2001234852A1
AU2001234852A1 AU2001234852A AU2001234852A AU2001234852A1 AU 2001234852 A1 AU2001234852 A1 AU 2001234852A1 AU 2001234852 A AU2001234852 A AU 2001234852A AU 2001234852 A AU2001234852 A AU 2001234852A AU 2001234852 A1 AU2001234852 A1 AU 2001234852A1
Authority
AU
Australia
Prior art keywords
vol
sec
maximum
base stock
pour point
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
AU2001234852A
Other versions
AU2001234852B2 (en
Inventor
Albert Gordon Alexander
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
ExxonMobil Technology and Engineering Co
Original Assignee
ExxonMobil Research and Engineering Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by ExxonMobil Research and Engineering Co filed Critical ExxonMobil Research and Engineering Co
Priority claimed from PCT/US2001/003790 external-priority patent/WO2001059038A1/en
Publication of AU2001234852A1 publication Critical patent/AU2001234852A1/en
Application granted granted Critical
Publication of AU2001234852B2 publication Critical patent/AU2001234852B2/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Description

FUNCTIONAL FLUID
BACKGROUND OF THE INVENTION
Functional fluids comprise a broad range of lubricants that are used in automotive and industrial hydraulic systems, automotive transmissions, power steering systems, shock absorber fluids, and the like. These fluids transmit and control power in mechanical systems, and thus must have carefully controlled viscometric characteristics. In addition, these fluids may sometimes be formulated to provide multigrade performance so as to ensure year round operation in variable climates.
Power Steering Fluids (PSF) are one of the most common functional fluids, and an integral part of all power steering systems. Power steering is used in about 80% to 90% of all vehicles in North America and Japan and their use is becoming more commonplace in other parts of the world. These systems are considered "safety sensitive" and the major OEMs have stringent specifications to control all aspects of the components that go into their manufacture, including the functional fluid.
A power steering system comprises a pump, gears, output drives and hydraulic system. The PSF acts as a hydraulic fluid to transfer power in the system and thus assist the driver to control the vehicle. Loss of control could lead to an accident and thus the fluid must have the right viscometrics at ambient start-up temperatures, while ma taining sufficient viscosity at higher operating temperatures. PSF must also be very oxidation stable since it is subjected to high temperatures and is expected to remain in service for up to 100,000 miles in some cases. In addition, and perhaps amongst the most important requirements for a power steering fluid is compatibility with seals and hoses, which can be measured in various ASTM tests, for example, D 471.
In the past power steering fluids generally used blends of naphthenic and solvent neutral base stocks, and their use is still common in many applications. However, over the past few years, with the increasing performance demands being made on power steering fluids, the use of "next generation" hydrocracked base stocks could offer oxidation advantages. However, such molecular compositional changes would not be expected to be compatible with the seals and hoses in power steering systems.
DESCRIPTION OF THE L VENTION
The present invention is directed to a functional fluid base oil which comprises:
(i) at least one naphthenic base stock having a kinematic viscosity of about 1.5 to about 3.5 mm2/sec at 100°C, preferably about 1.5 to about 2.5 mm.2/sec at 100°C, a viscosity index of about 90 or less, preferably about 80 or less, a pour point of about -42°C maximum, an aniline point of about 90°C or less and a saturates content of about 90 mass % or less; and
(ii) at least one conventional solvent neutral base stock having a kinematic viscosity of about 2.5 to about 6.5 mm2/sec at 100°C, preferably about 3.0 to about 5.5 mm2/sec at 100°C, a viscosity index of about 90 to about 105, preferably about 90 to about 100, a pour point of about -12°C maximum, preferably about -15°C maximum, an -uiiline point of about 95 to about 105°C, a saturates content of about 75 to about 90 mass %, preferably about 80 to about 90 mass %; and (iii) at least one hydrocracked base stock having a kinematic viscosity of about 3.5 to about 6.5 mm2/sec at 100°C, preferably about 3.8 to about 5 mm2/sec at 100°C, more preferably about 4.2 to about 4.8 mm2/sec at 100°C, a viscosity index of about 100 to about 120, preferably about 105 to about 120, more preferably about 110 to about 120, a pour point of about -12°C maximum, preferably about -15°C, more preferably about -18°C, an aniline point of about 100°C to about 120°C, preferably about 105°C to about 115°C, a saturates content of about 92 to about 99 mass %, preferably about 93 to about 99 mass %, more preferably about 94 to about 96 mass %;
wherein the naphthenic base stock (i) is present in an amount of about 15 vol% to about 45 vol%, preferably about 15 vol% to about 35 vol%;
wherein the solvent neutral base stock (ii) is present in an amount of about 15 vol% to about 45 vol%, preferably about 25 vol% to about 45 vol%;
wherein the hydrocracked base stock (iii) is present in an amount of about 15 vol% to about 45 vol%, preferably about 25 vol% to about 45 vol%;
(iv) optionally from about 0 vol% to about 30 vol%, preferably about 0 vol% to about 20 vol% of a second hydrocracked base stock comprising one or more hydrocracked bases stocks having a kinematic viscosity of about 1.5 to about 3.5 mm2/sec at 100°C, a viscosity index of about 90 or higher, a pour point of about -24°C maximum, an aniline point of about 95 to about 110°C, a saturates content of about 90 to about 99 mass %; said mixture of base stocks having a base stock blend kinematic viscosity of about 3 to about 5 mm2/sec at 100°C, preferably about 3.5 mm2/sec to about 4.5 mm2/sec at 100°C, a viscosity index of about 90 to about 115, preferably about 95 to about 110, a pour point of about -24°C maximum, preferably about -30°C maximum; and
(v) optionally at least one performance additive.
When the functional fluid is additized the resulting additized functional fluid has a kinematic viscosity of about 6.5 to about 9.5 mm2/sec at 100°C, preferably about 7.5 to about 8.5 mm2/sec at 100°C, a viscosity index of about 150 to about 200, a pour point of about -42°C maximum, and a Brookfield viscosity of about 25,000 cP or less at -40°C, preferably about 20,000 cP or less at -40°C, and meets seal compatibility requirements.
In the formulation the naphthenic base stock(s) and solvent neutral base stock(s) are those oils well known in the industry and produced by conventional techniques similarly well known in the petroleum industry.
The hydrocracked base stocks may be prepared by use of any of the hydrocracking process procedures currently used in the art, as well as any processes yet to be developed. It is believed the performance and function of the hydrocracked base stocks in the present invention are independent of the particular procedural techniques employed in the production of the base stocks. Typically hydrocracked base stocks are made starting with distillate from the atmosphere/vacuum pipestills and/or coker distillate, optionally subjecting such distillate to an aromatics removal step using an aromatics selective solvent such as phenol, furfural, NMP, etc. The distillate is then subjected to hydroconversion in at least one hydroconversion zone, more typically two zones whereas the distillate is exposed to a catalyst in the presence of hydrogen at high temperature and pressure to effect the saturation of aromatics, open rings and reduce sulfur and nitrogen content.
If the previously recited, optional aromatics removal step was not produced, the stream from the hydroconversion stage(s) can now be subject to an aromatics removal step such as solvent extraction employ a selective solvent such as phenol, furfural, NMP, etc. This stream can then be subjected to wax removal employing solvent dewaxing or catalytic dewaxing or isomerization. The stream, either before or after such dewaxing can also be subjected to hydro- finishing to further reduce the sulfur and nitrogen content.
Examples of suitable hychocracking processes can be found in "All Hydroprocessing Route for High Viscosity Index Lubes" Zakarian et al Energy Progress, Vol. 7, No. 1, pp. 59-64; "Hydrotreated Lube Oil Base Stocks" Cashmore et al, SAE Paper 821235; "Lube Facility Makes High Quality Lube Oil from Low Quality Feed" Farrell et al, Oil and Gas Journal, May 19, 1986, Technology, pp. 47-51, U.S. Patent 5,976,353.
Additives useful in preparing fully formulated functional fluid(s), especially power steering fluids include:
VI improvers generally of the polymethacrylate type, but also styrene esters, olefin copolymers, which may be non dispersant or dispersant, or mixtures thereof,
antiwear additives can be alkyl, aryl or alkyl/aryl phosphate esters, thiophosphates, sulphurized olefins, zinc dialkyldithiophosphates, or mixtures thereof, antioxidants such as phenolic, a ine, or combinations thereof,
antirust additives, copper corrosion or other metal deactivators,
friction modifiers such as glycerides, fatty acids, fatty amines, etc.,
pour point depressants,
antifoams such as silicone polymers, acrylate polymers.
Typically, a power steering additive package will be employed in an amount in the range of about 5 vol% to about 20 vol% as received, preferably about 6 vol% to about 16 vol% as received, wherein the maximum amount of diluent oil in the total additive package is between 0 to about 40 vol%.

Claims (2)

CLAIMS:
1. A functional fluid base oil comprising:
(i) at least one naphthenic base stock having a kinematic viscosity of about 1.5 to about 3.5 mm2/sec at 100°C, a viscosity index of about 90 or less, a pour point of about -42°C maximum, an aniline point of about 90°C or less, a saturates content of about 90 mass % or less;
(ii) at least one conventional solvent neutral base stock, having a kinematic viscosity of about 2.5 to about 6.5 mm2/sec at 100°C, a viscosity index of about 90 to about 105, a pour point of about -12°C maxi um, an aniline point of about 95°C to about 105°C, a saturates content of about 75 to about 90 mass %;
(iii) at least one hydrocracked base having a kinematic viscosity of about 3.5 to about 6.5 mm2/sec at 100°C, a viscosity index of about 100 to about 120, a pour point of about -12°C maximum, an aniline point of about 100°C to about 120°C, a saturates content of about 92 to about 99 mass %; wherein
the naphthenic base stock is present in the amount of about 15 vol% to about 45 vol%
the solvent neutral base stock is present in the amount of about 15 vol% to about 45 vol%
the hydrocracked base stock is present in the amount of about 15 vol% to about 45 vol%; (iv) optionally from about 0 vol% to about 30 vol% of a second hydrocracked base stock comprising one or more hydrocracked bases stocks having a kinematic viscosity of about 1.5 to about 3.5 mm2/sec at 100°C, a viscosity index of about 90 or higher, a pour point of about -24°C maximum, an ariiline point of about 95 to about 110°C, a saturates content of about 90 to about 99 mass %
said mixture of base stocks having a kinematic viscosity of about 3 to about 5 mm2/sec at 100°C, a viscosity index of about 90 to about 115, a pour point of about -24°C maximum.
2. The functional fluid base oil of claim 1 further containing (v) an additive package, the additized functional fluid having, a kinematic viscosity of about 6.5 to about 9.5 mm2/sec at 100°C, a viscosity index of about 150 to about 200, a pour point of about < -42°C maximum, and a Brookfield of about < 25,000 cP or less at -40°C.
AU2001234852A 2000-02-08 2001-02-06 Functional fluid Ceased AU2001234852B2 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US18113800P 2000-02-08 2000-02-08
US60/181,138 2000-02-08
PCT/US2001/003790 WO2001059038A1 (en) 2000-02-08 2001-02-06 Functional fluid

Publications (2)

Publication Number Publication Date
AU2001234852A1 true AU2001234852A1 (en) 2001-11-01
AU2001234852B2 AU2001234852B2 (en) 2004-11-11

Family

ID=22663051

Family Applications (2)

Application Number Title Priority Date Filing Date
AU3485201A Pending AU3485201A (en) 2000-02-08 2001-02-06 Functional fluid
AU2001234852A Ceased AU2001234852B2 (en) 2000-02-08 2001-02-06 Functional fluid

Family Applications Before (1)

Application Number Title Priority Date Filing Date
AU3485201A Pending AU3485201A (en) 2000-02-08 2001-02-06 Functional fluid

Country Status (9)

Country Link
US (1) US6426322B2 (en)
EP (1) EP1259579B1 (en)
JP (1) JP2003522277A (en)
AT (1) ATE284437T1 (en)
AU (2) AU3485201A (en)
CA (1) CA2397836C (en)
DE (1) DE60107660T2 (en)
NO (1) NO324313B1 (en)
WO (1) WO2001059038A1 (en)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20020016746A1 (en) * 2000-04-12 2002-02-07 Mchenry Michael E. Customized motor oil selection
US6544937B2 (en) * 2001-05-22 2003-04-08 Exxonmobile Research And Engineering Company Demulsification of industrial lubricants containing naphthenic basestocks
US20060191819A1 (en) * 2003-03-31 2006-08-31 Haines Thomas W Protective lubricant formulation
US7674364B2 (en) * 2005-03-11 2010-03-09 Chevron U.S.A. Inc. Hydraulic fluid compositions and preparation thereof
WO2006101206A1 (en) * 2005-03-25 2006-09-28 Mitsui Chemicals, Inc. Viscosity control agent for lubricant for power transfer system and lubricant composition for power transfer system
JP5101877B2 (en) * 2006-12-28 2012-12-19 Jx日鉱日石エネルギー株式会社 Hydraulic fluid composition for shock absorber
US9127229B2 (en) * 2009-07-24 2015-09-08 Cherron Oronite Technology B.V. Trunk piston engine lubricating oil compositions

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3915871A (en) * 1972-10-16 1975-10-28 Sun Oil Co Pennsylvania Composition comprising naphthenic distillate, hydro-cracked lube and an antioxidant
JPS5624493A (en) * 1979-08-06 1981-03-09 Nippon Oil Co Ltd Central system fluid composition for automobile
US4717489A (en) * 1984-05-09 1988-01-05 Standard Oil Company Heavy duty diesel engine oil blend
JPH0730346B2 (en) * 1986-09-08 1995-04-05 出光興産株式会社 Lubricating oil composition
US5064546A (en) * 1987-04-11 1991-11-12 Idemitsu Kosan Co., Ltd. Lubricating oil composition
US5167847A (en) * 1990-05-21 1992-12-01 Exxon Research And Engineering Company Process for producing transformer oil from a hydrocracked stock
US5344582A (en) * 1991-07-31 1994-09-06 Tonen Corporation Traction fluid derived from cyclopentadiene oligomers
US5321172A (en) * 1993-02-26 1994-06-14 Exxon Research And Engineering Company Lubricating composition for two-cycle internal combustion engines
US5520832A (en) * 1994-10-28 1996-05-28 Exxon Research And Engineering Company Tractor hydraulic fluid with wide temperature range (Law180)
JP3510368B2 (en) * 1995-01-31 2004-03-29 東燃ゼネラル石油株式会社 Lubricating oil composition for internal combustion engines
EP0856042B9 (en) * 1995-10-18 2011-12-21 Infineum USA L.P. Automatic transmission with an automatic transmission fluid of improved friction durability
JP2000501126A (en) * 1995-11-03 2000-02-02 エクソン・ケミカル・パテンツ・インク Automatic transmission fluid with improved transmission behavior
US6110879A (en) * 1998-10-15 2000-08-29 Chevron U.S.A. Inc. Automatic transmission fluid composition
US6187725B1 (en) * 1998-10-15 2001-02-13 Chevron U.S.A. Inc. Process for making an automatic transmission fluid composition

Similar Documents

Publication Publication Date Title
EP1920035B1 (en) Gear oil composition
JPS63280796A (en) Lubricating oil composition having improved temperature characteristic
CN103834459B (en) Lubricant oil composite
CN103339241A (en) Lubricating oil composition
JPS63280797A (en) Lubricating oil base oil and composition for mechanical device having orifice mechanism
WO2017163977A1 (en) Lubricant oil composition and lubrication method
KR100714141B1 (en) A use of c12-20 polyalkyl methacrylate polymer as lubricating oil additive
CN110225962A (en) Lubricating oil composition for transmission, method for lubricating transmission, and transmission
CN103502408B (en) Lubricant oil composite
EP1462510A1 (en) Gear lubricating composition
KR20140047606A (en) Lubricating oil composition
CA2397836C (en) Functional fluid
AU2001234852A1 (en) Functional fluid
US6255546B1 (en) Functional fluid with low Brookfield Viscosity
AU2001230872A1 (en) Functional fluid with low brookfield viscosity
JPH09208976A (en) Gear oil and its production
US20050043192A1 (en) Shear stable functional fluid with low brookfield viscosity
WO1998004658A1 (en) Base stocks for transmission/gear lubricants
JP2008502787A (en) Hydrocarbon composition for continuously variable transmissions to reduce metal scuffing and seizure on metal interfaces
CA2477999C (en) Shear stable functional fluid with low brookfield viscosity
CN113748189A (en) Lubricating oil composition for transmissions, method for producing same, method for lubricating transmission using lubricating oil composition for transmissions, and transmission
JP2555284C (en)