EP1857533A1 - Fluides de transmission de puissance - Google Patents

Fluides de transmission de puissance Download PDF

Info

Publication number
EP1857533A1
EP1857533A1 EP07107808A EP07107808A EP1857533A1 EP 1857533 A1 EP1857533 A1 EP 1857533A1 EP 07107808 A EP07107808 A EP 07107808A EP 07107808 A EP07107808 A EP 07107808A EP 1857533 A1 EP1857533 A1 EP 1857533A1
Authority
EP
European Patent Office
Prior art keywords
additive package
fluid composition
antiwear
antiwear additive
extreme pressure
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.)
Withdrawn
Application number
EP07107808A
Other languages
German (de)
English (en)
Inventor
Jeffrey L. Milner
David H. Colley
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.)
Afton Chemical Corp
Original Assignee
Afton Chemical Corp
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 Afton Chemical Corp filed Critical Afton Chemical Corp
Publication of EP1857533A1 publication Critical patent/EP1857533A1/fr
Withdrawn legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M141/00Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential
    • C10M141/10Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential at least one of them being an organic phosphorus-containing compound
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02Hydroxy compounds
    • C10M2207/023Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/028Overbased salts thereof
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/22Acids obtained from polymerised unsaturated acids
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/02Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/08Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate type
    • C10M2209/084Acrylate; Methacrylate
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/08Amides
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/086Imides
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/22Heterocyclic nitrogen compounds
    • C10M2215/223Five-membered rings containing nitrogen and carbon only
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/28Amides; Imides
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/10Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
    • C10M2219/104Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring containing sulfur and carbon with nitrogen or oxygen in the ring
    • C10M2219/106Thiadiazoles
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2221/00Organic macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2221/04Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2221/041Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds involving sulfurisation of macromolecular compounds, e.g. polyolefins
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/02Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
    • C10M2223/04Phosphate esters
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/02Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
    • C10M2223/049Phosphite
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2020/00Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
    • C10N2020/01Physico-chemical properties
    • C10N2020/071Branched chain compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/06Oiliness; Film-strength; Anti-wear; Resistance to extreme pressure
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/08Resistance to extreme temperature

Definitions

  • the present disclosure relates to an additive concentrate and lubricant composition that provides balanced performance for lubricating wet multi-disk brakes and/or differentials suitable for off-road vehicles while providing bearing and gear pitting protections with relatively low gear wear.
  • the combination of additives in the concentrate provides relatively low static friction for limited slip performance and relatively high dynamic friction for enhanced braking performance.
  • Gear fluids incorporate various additives in an effort to improve and control friction and wear properties of the fluid.
  • conventional gear fluids and additives therefore are not suited for all applications.
  • all-wheel drives (AWD) and off-road vehicles having wet multi-disk brakes and/or differentials require lubricants that must meet other criteria such as ZF TE-ML 05 specifications.
  • a viscous coupling is commonly installed on the propeller shaft in order to transmit torque while still allowing some difference in rotational speeds between front and rear axle.
  • the disadvantage of a viscous coupling is that it is not controllable during operation and therefore does not work well in combination with electronic driving aid systems such as electronic stability programs and traction control systems. Accordingly, improved traction control systems have been developed that include an active-on-demand AWD system for vehicles with short system activation and deactivation times.
  • One such AWD system features a multiple disc wet clutch with clutch plates covered with a sintered friction material.
  • the clutch pack distributes drive torque to the rear axle of the vehicle.
  • torque transfer control is enhanced which makes it possible to electronically control the drive torque distribution between the front and rear axle in order to optimize vehicle dynamics.
  • a cam on the rear axle causes a pumping action on a hydraulic piston pump.
  • the hydraulic pressure generated is applied to the clutch pack in order to reduce the speed difference between the shafts, thus engaging the all-wheel drive.
  • the torque transmitted by the coupling is controlled by a throttle valve.
  • Fluids suitable for use in AWD vehicle wet disk brakes and/or differentials include one or more base oils and one or more additives. Such fluids must provide adequate friction performance and at the same time have good shear and oxidation stability, anti-wear performance and corrosion resistance. The concentration of each additive in the fluids, and the balance between them, is important when formulating such fluids.
  • a fluid composition for all-wheel drive wet multi-disk brakes and/or differentials having improved characteristics, additive concentrates for all-wheel drive vehicles and methods for improving fluid characteristics for all-wheel drive vehicles.
  • the fluid composition is a base oil containing an extreme pressure/antiwear additive package, and a limited slip/antiwear additive package.
  • the composition is substantially devoid of zinc containing additives and is substantially devoid of dithiophosphate components and includes from about 1000 to about 2000 ppm phosphorous from phosphorous-containing components based on a total weight of the fluid composition.
  • the disclosure provides an additive concentrate for an all-wheel drive vehicle fluid.
  • the additive concentrate includes an extreme pressure/antiwear additive package and a limited slip/antiwear additive package.
  • the fluid containing the additive concentrate is substantially devoid of zinc containing components and is substantially devoid of dithiophosphate containing components.
  • Yet another exemplary embodiment of the disclosure provides a lubricant composition having an extreme pressure/antiwear package and a limited slip/antiwear additive package.
  • the limited slip/antiwear additive package contains a dialkyl hydrogen phosphite, and provides improved high temperature performance for the lubricant composition.
  • the additive combination described herein may provide balanced performance for lubricating wet multi-disk brakes and/or differentials for all-wheel drive or off-road vehicles while providing bearing and gear pitting protection with low gear wear.
  • a unique mixture of phosphite, rust inhibitor, and static and dynamic friction modifiers in effective amounts may provide balanced performance needs for off-road axles with multi-disk brakes and/or differentials.
  • "Balanced performance,” as used herein, means that the additive may provide both low static friction for limited slip performance and high dynamic friction for brake performance.
  • the limited slip/antiwear additive package described herein may enable a lubricant composition to maintain its API GL-5 performance characteristics.
  • the limited slip/antiwear additive package may also enable a lubricant composition to possess high temperature, load bearing characteristics according to L-37 specifications.
  • hydrocarbyl substituent or “hydrocarbyl group” is used in its ordinary sense, which is well-known to those skilled in the art. Specifically, it refers to a group having a carbon atom directly attached to the remainder of a molecule and having a predominantly hydrocarbon character. Examples of hydrocarbyl groups include:
  • percent by weight means the percentage the recited component represents to the weight of the entire composition.
  • the fluid compositions described herein will contain from about 80 to about 98 percent by weight of a base oil.
  • fluid compositions as provided herein may be based on natural or synthetic oils, or blends thereof, provided the base oil has a suitable viscosity for use in the applications described.
  • the base oils will normally have a viscosity in the range of SAE 50 to SAE 250, and more usually will range from SAE 70W to SAE 140.
  • Suitable base oils may also include cross-grades such as 75W-140, 80W-90, 85W-140, 85W-90, and the like.
  • Base oils suitable for use herein may be made using a variety of different processes including but not limited to distillation, solvent refining, hydrogen processing, oligomerization, esterification, and re-refining.
  • API 1509 "Engine Oil Licensing and Certification System” Fourteenth Edition, December 1996 states that all base oils are divided into five general categories:
  • test methods used in defining the above groups are ASTM D2007 for saturates; ASTM D2270 for viscosity index; and one of ASTM D2622, 4294, 4927 and 3120 for sulfur.
  • Group IV base oils i.e. polyalphaolefins (PAO) include hydrogenated oligomers of an alpha-olefin, the most important methods of oligomerization being free radical processes, Ziegler catalysis, and cationic, Friedel-Crafts catalysis.
  • PAO polyalphaolefins
  • the polyalphaolefins typically have viscosities in the range of 2 to 100 cSt at 100° C., preferably 4 to 8 cSt at 100° C. They may, for example, be oligomers of branched or straight chain alphaolefins having from 2 to 16 carbon atoms, specific examples being polypropenes, polyisobutenes, poly-1-butenes, poly-1-hexenes, poly-1-octenes and poly-1-decene. Included are homopolymers, interpolymers and mixtures.
  • a base oil referred to above as a "Group I base oil” may include a major amount of Group I base oil and a minor amount of base oil(s) from one or more other groups, provided that the resulting admixture has characteristics falling within those specified above for Group I base oils.
  • Preferred base oils include Group I base oils and mixtures of Group II base oils with Group I base oils.
  • Fluid compositions and additive concentrates described herein include a limited slip additive package containing one or more dispersants, a detergent, a friction modifier, a rust inhibitor, and a limited slip agent.
  • the limited slip/antiwear additive package of the present disclosure may contain at least one dispersant.
  • the dispersant may comprise an ashless dispersant having basic nitrogen and/or at least one hydroxyl group in the molecule, such as a succinimide dispersant, succinic ester dispersant, succinic ester-amide dispersant, Mannich base dispersant, hydrocarbyl polyamine dispersant, or polymeric polyamine dispersant.
  • the dispersants suitable for use also include non-phosphorus-containing dispersants, the phosphorus-containing dispersants described above as well as mixtures of phosphorus and non-phosphorus-containing, dispersants.
  • Polyamine succinimides in which the succinic group contains a hydrocarbyl substituent containing at least 30 carbon atoms are described for example in U.S. Pat. Nos. 3,972,892 ; 3,202,678 ; 3,216,936 ; 3,219,666 ; 3,254,025 ; 3,272,746 ; and 4,234,435 .
  • the alkenyl succinimides may be formed by conventional methods such as by heating an alkenyl succinic anhydride, acid, acid-ester, acid halide, or lower alkyl ester with a polyamine containing at least one primary amino group.
  • the alkenyl succinic anhydride may be made readily by heating a mixture of olefin and maleic anhydride to, for example, about 180-220° C.
  • the olefin may be a polymer or copolymer of a lower monoolefin such as ethylene, propylene, 1-butene, isobutene and the like and mixtures thereof.
  • the source of alkenyl group is from polyisobutene having a gel permeation chromatography (GPC) number average molecular weight of up to about 10,000 or higher, or alternatively in the range of about 500 to about 2,500, or further alternatively in the range of about 800 to about 1,200.
  • GPC gel permeation chromatography
  • succinimide is meant to encompass the completed reaction product from a reaction between one or more polyamine reactants and a hydrocarbon-substituted succinic acid or anhydride (or like succinic acylating agent), and is intended to encompass compounds wherein the product may have amide, amidine, and/or salt linkages in addition to the imide linkage of the type that results from the reaction of a primary amino group and an anhydride moiety.
  • Alkenyl succinic acid esters and diesters of polyhydric alcohols containing about 2 to about 20 carbon atoms and about 2 to about 6 hydroxyl groups can be used in forming ashless dispersants. Representative examples are described in U.S. Pat. Nos. 3,339,776 ; 3,381,022 ; and 3,522,179 .
  • the alkenyl succinic portion of these esters corresponds to the alkenyl succinic portion of the succinimides described above.
  • Suitable alkenyl succinic ester-amides for forming the phosphorylated ashless dispersant are described for example in U.S. Pat. Nos. 3,184,474 ; 3,576,743 ; 3,632,511 ; 3,804,763 ; 3,836,471 ; 3,852,981 ; 3,936,480 ; 3,948,800 ; 3,950,341 ; 3,957,854 ; 3,957,855 ; 3,991,098 ; 4,071,548 ; and 4,173,540 .
  • Hydrocarbyl polyamine dispersants that may be phosphorylated are generally produced by reacting an aliphatic or alicyclic halide (or mixture thereof) containing an average of at least about 40 carbon atoms with one or more amines, preferably polyalkylene polyamines. Examples of such hydrocarbyl polyamine dispersants are described in U.S. Pat. Nos. 3,275,554 ; 3,394,576 ; 3,438,757 ; 3,454,555 ; 3,565,804 ; 3,671,511 ; and 8,821,302 .
  • the hydrocarbyl-substituted polyamines are high molecular weight hydrocarbyl-N-substituted polyamines containing basic nitrogen in the molecule.
  • the hydrocarbyl group typically has a number average molecular weight in the range of about 750 to about 10,000 as determined by GPC, more usually in the range of about 1,000 to about 5,000, and is derived from a suitable polyolefin.
  • Some hydrocarbyl-substituted amines or polyamines are prepared from polyisobutenyl chlorides and polyamines having from about 2 to about 12 amine nitrogen atoms and from about 2 to about 40 carbon atoms.
  • Mannich polyamine dispersants which may be used to form phosphorylated ashless dispersant are a reaction product of an alkyl phenol, typically having a long chain alkyl substituent on the ring, with one or more aliphatic aldehydes containing from about 1 to about 7 carbon atoms (especially formaldehyde and derivatives thereof, and polyamines (especially polyalkylene polyamines). Examples of Mannich condensation products, and methods for their production are described in numerous U.S. Patents.
  • hydrocarbon sources for preparation of the Mannich polyamine dispersants are those derived from substantially saturated petroleum fractions and olefin polymers, preferably polymers of mono-olefins having from about 2 to about 6 carbon atoms.
  • the hydrocarbon source generally contains at least about 40 and preferably at least about 50 carbon atoms to provide substantial oil solubility to the dispersant.
  • the olefin polymers having a GPC number average molecular weight between about 600 and about 5,000 are preferred for reasons of easy reactivity and low cost. However, polymers of higher molecular weight can also be used.
  • Especially suitable hydrocarbon sources are isobutylene polymers.
  • Mannich base dispersants that may be used are Mannich base ashless dispersants formed by condensing about one molar proportion of long chain hydrocarbon-substituted phenol with from about 1 to about 2.5 moles of formaldehyde and from about 0.5 to about 2 moles of polyalkylene polyamine.
  • Polymeric polyamine dispersants suitable for preparing phosphorylated ashless dispersants are polymers containing basic amine groups and oil solubilizing groups (for example, pendant alkyl groups having at least about 8 carbon atoms). Such materials are illustrated by interpolymers formed from various monomers such as decyl methacrylate, vinyl decyl ether or relatively high molecular weight olefins, with aminoalkyl acrylates and aminoalkyl acrylamides. Examples of polymeric polyamine dispersants are set forth in U.S. Pat. Nos. 3,329,658 ; 3,449,250 ; 3,493,520 ; 3,519,565 ; 3,666,730 ; 3,687,849 ; and 3,702,300 .
  • the formulation of a limited slip/antiwear additive composition may include from about 1 wt. % to about 20 wt. % of one or more dispersants based on the total weight of the additive composition.
  • the formulation of a finished fluid composition for wet multi-disk brakes and/or differentials may include about 0.05 wt. % to about 5 wt. % of the one or more dispersants.
  • a mixture of a 900 to 2000 MW by GPC hydrocarbyl succinimide with a 1500 to 3000 MW by GPC borated phosphorylated hydrocarbyl succinimide in a ratio of about 2.0 to 2.5: 1 may be particularly useful in the additive described herein.
  • Metal-containing or ash-forming detergents function both as detergents to reduce or remove deposits and as acid neutralizers or rust inhibitors, thereby reducing wear and corrosion.
  • Detergents generally comprise a polar head with a long hydrophobic tail where the polar head comprises a metal salt of an acidic organic compound.
  • the salts may contain a substantially stoichiometric amount of the metal, in which case they are usually described as normal or neutral salts, and would typically have a total base number or TBN (as measured by ASTM D2896) of from 0 to less than 200.
  • TBN total base number
  • Large amounts of a metal base may be included by reacting an excess of a metal compound such as an oxide or hydroxide with an acidic gas such as carbon dioxide.
  • the resulting overbased detergent comprises micelles of neutralized detergent surrounding a core of inorganic metal base (e.g., hydrated carbonates).
  • Such overbased detergents may have a TBN of 150 or greater, and typically ranging from 250 to
  • Detergents that may be used include oil-soluble neutral and overbased sulfonates, phenates, sulfurized phenates, and salicylates of a metal, particularly the alkali or alkaline earth metals, e.g., sodium, potassium, lithium, calcium, and magnesium.
  • the most commonly used metals are calcium and magnesium, which may both be present. Mixtures of calcium and/or magnesium with sodium are also useful.
  • Particularly convenient metal detergents are neutral and overbased calcium or magnesium sulfonates having a TBN of from 20 to 450 TBN, neutral and overbased calcium or magnesium phenates and sulfurized phenates having a TBN of from 50 to 450, and neutral or overbased calcium or magnesium salicylates having a TBN of from 130 to 350. Mixtures of such salts may also be used.
  • the amount of detergent in the limited slip/antiwear additive package may range from about 1 wt. % to about 5 wt.%.
  • a finished lubricant composition according to the disclosed embodiments may include from about 0.05 to about 1.5 percent by weight detergent based on the total weight of the finished lubricant composition.
  • embodiments of the present disclosure may comprise a succinimide prepared from an alkenyl succinic acid or anhydride and ammonia.
  • the friction modifier may comprise the reaction product of a succinic anhydride and ammonia.
  • the alkenyl group of the alkenyl succinic acid may be a short chain alkenyl group, for example, the alkenyl group may comprise about 12 to about 36 carbon atoms.
  • the friction modifier may comprise a C 12 to C 36 aliphatic hydrocarbyl succinimide.
  • the friction modifier may comprise a C 16 to C 28 aliphatic hydrocarbyl succinimide.
  • the friction modifier may comprise a C 18 to about C 24 aliphatic hydrocarbyl succinimide.
  • the succinimide may be prepared from a succinic anhydride and ammonia as described in European Patent 0 020 037 , herein incorporated by reference. In some embodiments, no metallic or non-metallic friction modifier other than the succinimide disclosed herein is included.
  • the fully formulated lubricant may comprise a friction-modifying amount of the succinimide friction modifier. Further, for example, the lubricant may comprise about 0.05 wt% to about 1.5 wt% of the succinimide friction modifier.
  • tertiary alkyl primary amine useful as a rust inhibitor.
  • tertiary aliphatic primary amines are monoamines represented by the formula wherein R is a hydrocarbyl group containing from one to about 30 carbon atoms.
  • Such amines may be illustrated by tertiary-butyl amine, tertiary-hexyl primary amine, 1-methyl-1-amino-cyclohexane, tertiary-octyl primary amine, tertiary-decyl primary amine, tertiary-dodecyl primary amine, tertiary-tetradecyl primary amine, tertiary-hexadecyl primary amine, tertiary-octadecyl primary amine, tertiary-tetracosanyl primary amine, tertiary-octacosanyl primary amine.
  • amines are also useful for the purposes of the disclosed embodiments.
  • Illustrative of amine mixtures of this type are mixtures of C 11 -C 14 tertiary alkyl primary amines and mixtures of C 18 -C 22 tertiary alkyl primary amines.
  • the tertiary alkyl primary amines and methods for their preparation are well known to those of ordinary skill in the art and, therefore, further discussion is unnecessary.
  • the tertiary alkyl primary amine useful for the purposes described herein and methods for their preparation are described in U.S. Pat. No. 2,945,749 which is hereby incorporated by reference for its teaching in this regard.
  • the limited slip/antiwear additive package includes a limited slip agent such as a dihydrocarbyl hydrogen phosphite.
  • Suitable dihydrocarbyl hydrogen phosphites may be selected from the group consisting of dibutyl hydrogen phosphite, dipentyl hydrogen phosphite, di-2-ethylhexyl hydrogen phosphite, dipalmityl hydrogen phosphite, dilauryl hydrogen phosphite, distearyl hydrogen phosphite, dioleyl hydrogen phosphite, and other C 3 -C 30 alkyl or alkenyl acid phosphites, dicresyl hydrogen phosphite, and other C 6 -C 30 aryl acid phosphites, and mixtures thereof.
  • the dihydrocarbyl hydrogen phosphites have hydrocarbyl groups that may independently vary from
  • the dihydrocarbyl hydrogen phosphite may be added to a fully formulated fluid composition or may be included in an additive concentrate package.
  • the formulation of an additive concentrate package may include about 40 wt. % to about 75 wt. % of dihydrocarbyl hydrogen phosphite.
  • the fully formulated fluid composition may include from about 1.0 wt. % to about 10 wt. % of dihydrocarbyl hydrogen phosphite sufficient to provide from about 1000 to about 200 parts per million by weight of phosphorus in the fully formulated fluid composition.
  • the limited slip/antiwear additive package provided herein may contain a suitable diluent oil.
  • the diluent oil typically is present in the additive concentrates in a major amount.
  • a useful diluent is an oleaginous diluent of suitable viscosity. Such a diluent may be derived from natural or synthetic sources, or blends thereof.
  • Use of mineral oils as the diluent for the additive concentrate are particularly suitable. Among the mineral (hydrocarbonaceous) oils are paraffin base, naphthenic base, asphaltic base, and mixed base oils.
  • Synthetic oils include polyolefin oils (especially hydrogenated ⁇ -olefin oligomers), alkylated aromatics, polyalkylene oxides, aromatic ethers, and carboxylate esters (especially diesters), among others.
  • the diluents may be light hydrocarbon base oils, both natural and (per a) synthetic.
  • the diluent oil has a viscosity in the range of about 1 to about 40 cSt at 100° C., and typically about 2 to about 15 cSt at 100° C.
  • the diluent oil is a 150 Neutral mineral oil having a viscosity of about 6 cSt at 100° C.
  • the amount of diluent oil in the limited slip/antiwear additive package may range from about 30 to about 60 % by weight based on a total weight of the additive package.
  • the limited slip/antiwear additive component described above may be included in an extreme pressure/antiwear additive package concentrate or may be added to a lubricant containing an extreme pressure/antiwear additive package to provide the limited slip performance characteristics.
  • An extreme pressure/antiwear additive package that may be used with the limited slip/antiwear additive component may include extreme pressure agents, antiwear components, corrosion and/or rust inhibitors, antifoam agents, and a diluent oil.
  • sulfur-containing extreme pressure agents include, but are not limited to, dihydrocarbyl polysulfides, sulfurized olefins, sulfurized fatty acid esters of both natural (e.g. sperm oil) and synthetic origins, sulfurized terpenes, sulfurized oligomers of C 2 -C 8 monoolefins, and sulfurized Diels-Alder adducts such as those disclosed in reissue U.S. Pat. No. 21,331 , the disclosure of which is incorporated herein by reference.
  • sulfurized polyisobutene sulfurized isobutylene, sulfurized triisobutene, dicyclohexyl polysulfide, diphenyl and dibenzyl polysulfide, di-tert-butyl polysulfide, and dinonyl polysulfide, among others.
  • the sulfur-containing extreme pressure agent is at least one dimercaptothiadiazole or an oil-soluble derivative thereof.
  • Such materials provide extreme pressure and/or antiwear properties to exemplary fluid compositions described herein.
  • Dimercaptothiadiazoles which may be used in the fluid compositions include, but are not limited to, 2,5-dimercapto-1,3,4-thiadlazoles (DMTD) of the following formula: wherein R1 and R2 are selected from hydrogen and straight and branched chain alkyl groups having from 1 to 30 carbon atoms, and a and b are independently selected from integers ranging from 1 to 3.
  • DMTD may be prepared by reacting of one mole of hydrazine, or a hydrazine salt, with two moles of carbon disulfide in an alkaline medium, followed by acidification.
  • Fluid compositions described herein may include DMTD or derivatives of DMTD as set forth in the foregoing formula.
  • DMTD or derivatives of DMTD as set forth in the foregoing formula.
  • U.S. Pat. Nos. 2,719,125 ; 2,719,126 ; and 3,087,937 describe the preparation of various 2,5-bis(hydrocarbon dithio)-1,3,4-thiadiazoles.
  • the total amount of sulfur in the fluid composition that is provided by the sulfur-containing additives may range from about 0.5 to about 5.0 weight percent based on the total weight of the lubricant composition containing the additive package.
  • Suitable antiwear agents may include phosphorus-containing antiwear agents such as organic esters of phosphoric acid, phosphorous acid, or amine salts thereof.
  • the phosphorus-containing antiwear agent may include one or more of a monohydrocarbyl phosphate, a dihydrocarbyl phosphate, a trihydrocarbyl phosphate, any sulfur analogs thereof, and any amine salts thereof.
  • the phosphorus-containing antiwear agent may include at least one of 2-ethyl hexyl acid phosphate, dibutyl hydrogen phosphate, amyl acid phosphate, an amine salt of sulfurized dibutyl hydrogen phosphate, or dialkyl thiophosphoric acid.
  • the phosphorus-containing antiwear agent may be present in an amount sufficient to provide about 50 to about 500 parts per million by weight of phosphorus in the fully formulated lubricant composition.
  • the phosphorus-containing antiwear agent may be present in an amount sufficient to provide about 150 to about 350 parts per million by weight of phosphorus in the fluid composition.
  • Rust or corrosion inhibitors are another preferred type of inhibitor additive for use in fluid compositions described herein.
  • Such materials include monocarboxylic acids and polycarboxylic acids.
  • suitable monocarboxylic acids are octanoic acid, decanoic acid and dodecanoic acid.
  • Suitable polycarboxylic acids include dimer and trimer acids such as are produced from such acids as tall oil fatty acids, oleic acid, linoleic acid, or the like. Products of this type are currently available from various commercial sources.
  • rust inhibitor for use in the compositions described herein is comprised of the alkenyl succinic acid and alkenyl succinic anhydride corrosion inhibitors such as, for example, tetrapropenylsuccinic acid, tetrapropenylsuccinic anhydride, tetradecenylsuccinic acid, tetradecenylsuccinic anhydride, hexadecenylsuccinic acid, hexadecenylsuccinic anhydride, and the like.
  • the half esters of alkenyl succinic acids having 8 to 24 carbon atoms in the alkenyl group with alcohols such as the polyglycols.
  • Suitable rust or corrosion inhibitors include ether amines; acid phosphates; amines; polyethoxylated compounds such as ethoxylated amines, ethoxylated phenols, and ethoxylated alcohols; imidazolines; aminosuccinic acids or derivatives thereof, and the like. Materials of these types are available as articles of commerce. Mixtures of such rust or corrosion inhibitors may be used. The amount of corrosion inhibitor in the additive package may range from about 0.01 to about 0.5 weight percent based on the total weight of the formulation.
  • rust inhibitor that may be used is a tertiary alkyl primary amine.
  • tertiary aliphatic primary amines are monoamines represented by the formula wherein R is a hydrocarbyl group containing from one to about 30 carbon atoms.
  • Such amines may be illustrated by tertiary-butyl amine, tertiary-hexyl primary amine, 1-methyl-1-amino-cyclohexane, tertiary-octyl primary amine, tertiary-decyl primary amine, tertiary-dodecyl primary amine, tertiary-tetradecyl primary amine, tertiary-hexadecyl primary amine, tertiary-octadecyl primary amine, tertiary-tetracosanyl primary amine, tertiary-octacosanyl primary amine.
  • amines are also useful for the purposes of the disclosed embodiments. Illustrative of amine mixtures of this type are mixtures of C 11 -C 14 tertiary alkyl primary amines and mixtures of C 18 -C 22 tertiary alkyl primary amines.
  • the tertiary alkyl primary amines and methods for their preparation are well known to those of ordinary skill in the art and, therefore, further discussion is unnecessary.
  • the tertiary alkyl primary amine useful for the purposes described herein and methods for their preparation are described in U.S. Pat. No. 2,945,749 which is hereby incorporated by reference for its teaching in this regard.
  • the amount of tertiary alky primary amine in the additive package may range from about 0.5 to about 5.0 weight percent based on a total weight of the additive package.
  • a foam inhibitor forms another component suitable for use in the compositions described herein.
  • Foam inhibitors may be selected from silicones, polyacrylates, surfactants, and the like.
  • the amount of antifoam agent in the additive package described herein may range from about 0.01 to about 0.1 weight percent based on the total weight of the lubricant composition.
  • the additive package provided herein may contain a suitable process oil.
  • the process oil typically is present in the additive concentrates in a major amount.
  • a useful process oil is an oleaginous diluent of suitable viscosity.
  • Such an oil may be derived from natural or synthetic sources, or blends thereof.
  • Use of mineral oils as the process oil for the additive concentrate are particularly suitable.
  • the mineral (hydrocarbonaceous) oils are paraffin base, naphthenic base, asphaltic base, and mixed base oils.
  • Synthetic oils include polyolefin oils (especially hydrogenated ⁇ -olefin oligomers), alkylated aromatics, polyalkylene oxides, aromatic ethers, and carboxylate esters (especially diesters), among others.
  • the process oils may be light hydrocarbon base oils, both natural and (per a) synthetic.
  • the process oil has a viscosity in the range of about 1 to about 40 cSt at 100° C., and typically about 2 to about 15 cSt at 100° C.
  • the process oil is a 150 Neutral mineral oil having a viscosity of about 6 cSt at 100° C.
  • the amount of process oil in the additive package may range from about 1 to about 10 percent by weight based on a total weight of the additive package.
  • Additives used in formulating the fluid compositions described herein may be blended into the base oil individually or in various sub-combinations. However, it is preferable to blend all of the components concurrently using an additive concentrate (i.e., additives plus a diluent, such as a hydrocarbon solvent described above).
  • an additive concentrate i.e., additives plus a diluent, such as a hydrocarbon solvent described above.
  • the use of an additive concentrate takes advantage of the mutual compatibility afforded by the combination of ingredients when in the form of an additive concentrate. Also, the use of a concentrate reduces blending time and lessens the possibility of blending errors.
  • the fluid compositions containing the additives described above may be further characterized as having a substantial absence of zinc-containing components. Further the fluid compositions may be further characterized as having a substantial absence of dithiophosphate-containing components.
  • Exemplary additive concentrates that may be combined for balanced limited slip performance and enhanced multi-disk braking for off-road vehicles according to the disclosure may be provided by the following compositions: Table 1 Limited Slip/Antiwear Package (LS Additive) Wt. % 1300 MW succinimide dispersant 1 to 5 Borated, phosphorylated dispersant 0.5 to 1.5 Tertiary alkyl primary amine 5 to 15 Succinimide friction modifier 1 to 5 Calcium phenate detergent 1 to 5 Dihydrocarbyl hydrogen phosphite 20 to 50 Diluent oil 20 to 50 Table 2 Extreme Pressure/Antiwear Package (EP Additive) Wt.
  • Table 1 Limited Slip/Antiwear Package LS Additive
  • succinimide dispersant 1 to 5 Borated, phosphorylated dispersant 0.5 to 1.5 Tertiary alkyl primary amine 5 to 15
  • Succinimide friction modifier 1 to 5
  • Calcium phenate detergent 1 to 5 Dihydrocarbyl hydrogen phosphite 20 to 50 Dil
  • the additive package of Table 1 provided improvement in the rust inhibitor performance (as indicated by the L-33-1 test) compared to a GL-5 oil containing only the additive package of Table 2.
  • the additive also provided a passing L-37 high temperature grade to an otherwise failing GL-5 oil.
  • the additive package of Table 1 also contributed no significant detrimental effects under the GL-5 testing criteria.
  • the additive package of Table 1 may provide a balanced performance for lubricating wet multi-disk brakes and/or differentials while providing bearing and gear pitting protections with relatively low gear wear.
  • the additive package of Table 1 may also be used as a top treat to differentials in passenger vehicles to provide improved limited slip performance.
  • lubricants containing the additive packages of Table 1 and Table 2 were compared to conventional gear oils and to oils containing conventional additive packages.
  • Sample 1 is a gear oil containing a tractor hydraulic fluid additive package.
  • Sample 2 is a conventional GL-5 gear oil.
  • Samples 3 and 4 are the same gear oils of Sample 2 with the additive package of Table 2.
  • Sample 3 contains a conventional limited slip package and
  • Sample 4 contains the limited slip package of Table 1.
  • Samples 5-8 contain are gear oils containing conventional extreme pressure and limited slip additive packages.
  • Samples 5 and 6 were the same oils with and without the conventional limited slip additive package 1.
  • Samples 7 and 8 were the same oils with and without the conventional limited slip additive package 2.
  • Sample 4 containing the additives of Table 1 and Table 2 not only provided suitable TE ML 05C performance, but also passed the GL-5 test and the high temperature L-37 test.
  • Sample 2 containing only the additive package of Table 2 passed the GL-5 test but failed most of the other tests.
  • Sample 3 containing the additive package of Table 2 and a conventional limited slip (LS) additive failed the GL-5 test but passed some of the other tests.
  • the other samples (5-8) containing conventional EP and LS additives were likewise inferior to Sample 4 since they either failed the GL-5 test or the axle brake test and SAE #2 dynamic friction test.
  • each numerical parameter should at least be construed in light of the number of reported significant digits and by applying ordinary rounding techniques. Notwithstanding that the numerical ranges and parameters setting forth the broad scope of the invention are approximations, the numerical values set forth in the specific examples are reported as precisely as possible. Any numerical value, however, inherently contains certain errors necessarily resulting from the standard deviation found in their respective testing measurements. It is intended that the specification and examples be considered as exemplary only, with a true scope and spirit of the invention being indicated by the following claims.
EP07107808A 2006-05-19 2007-05-09 Fluides de transmission de puissance Withdrawn EP1857533A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US80220206P 2006-05-19 2006-05-19
US11/740,012 US20070270317A1 (en) 2006-05-19 2007-04-25 Power Transmission Fluids

Publications (1)

Publication Number Publication Date
EP1857533A1 true EP1857533A1 (fr) 2007-11-21

Family

ID=38426537

Family Applications (1)

Application Number Title Priority Date Filing Date
EP07107808A Withdrawn EP1857533A1 (fr) 2006-05-19 2007-05-09 Fluides de transmission de puissance

Country Status (3)

Country Link
US (1) US20070270317A1 (fr)
EP (1) EP1857533A1 (fr)
CN (1) CN101100625B (fr)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2453586C1 (ru) * 2011-03-29 2012-06-20 Государственное образовательное учреждение Высшего профессионального образования Волгоградский государственный технический университет (ВолГТУ) Трасмиссионное масло
WO2012087781A1 (fr) * 2010-12-21 2012-06-28 The Lubrizol Corporation Copolymères fonctionnalisés et compositions lubrifiantes à base de ceux-ci

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011031659A1 (fr) * 2009-09-14 2011-03-17 The Lubrizol Corporation Composition lubrifiante de tracteur agricole à bonne tolérance à l’eau
US20120238481A1 (en) * 2009-12-03 2012-09-20 Idemitsu Kosan Co., Ltd. Lubricating oil composition
CN103917632B (zh) * 2011-11-11 2015-06-24 范德比尔特化学品有限责任公司 润滑剂组合物

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4031023A (en) * 1976-02-19 1977-06-21 The Lubrizol Corporation Lubricating compositions and methods utilizing hydroxy thioethers
US4344854A (en) * 1975-03-21 1982-08-17 The Lubrizol Corporation Sulfurized compositions
US4752416A (en) * 1986-12-11 1988-06-21 The Lubrizol Corporation Phosphite ester compositions, and lubricants and functional fluids containing same
EP0399764A1 (fr) * 1989-05-22 1990-11-28 Ethyl Petroleum Additives Limited Compositions lubrifiantes
EP0646639A1 (fr) * 1993-08-20 1995-04-05 The Lubrizol Corporation Compositions lubrifiantes
EP0695799A2 (fr) * 1994-08-03 1996-02-07 The Lubrizol Corporation Une combination d'un composé de soufre et des composés spécifiques de phosphore et leurs utilisation dans des compositions lubrifiantes, des concentrés et des graisses
WO2000071646A1 (fr) * 1999-05-24 2000-11-30 The Lubrizol Corporation Huiles minerales pour engrenages et liquides a transmissions
US6534451B1 (en) * 2002-04-05 2003-03-18 Infineum International Ltd. Power transmission fluids with improved extreme pressure lubrication characteristics and oxidation resistance
EP1624043A2 (fr) * 2004-07-28 2006-02-08 Afton Chemical Corporation Fluides de transport de force motrice ayant des caractéristiques de pression extrême et d'anti-usure améliorées

Family Cites Families (51)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2719125A (en) * 1952-12-30 1955-09-27 Standard Oil Co Oleaginous compositions non-corrosive to silver
US2719126A (en) * 1952-12-30 1955-09-27 Standard Oil Co Corrosion inhibitors and compositions containing same
US2945749A (en) * 1956-04-18 1960-07-19 Socony Mobil Oil Co Inc Stabilized fuel oil containing tertiary alkyl primary amines
DE1248643B (de) * 1959-03-30 1967-08-31 The Lubrizol Corporation, Cleveland, Ohio (V. St. A.) Verfahren zur Herstellung von öllöslichen aeylierten Aminen
NL124842C (fr) * 1959-08-24
US3053341A (en) * 1960-01-08 1962-09-11 Gen Motors Corp Lubricant additive
US3087937A (en) * 1961-03-22 1963-04-30 Tesi Giorgio Bis (perfluoromethyl) phosphinic nitride
US3087936A (en) * 1961-08-18 1963-04-30 Lubrizol Corp Reaction product of an aliphatic olefinpolymer-succinic acid producing compound with an amine and reacting the resulting product with a boron compound
US3449250A (en) * 1962-05-14 1969-06-10 Monsanto Co Dispersency oil additives
US3329658A (en) * 1962-05-14 1967-07-04 Monsanto Co Dispersency oil additives
US3184474A (en) * 1962-09-05 1965-05-18 Exxon Research Engineering Co Reaction product of alkenyl succinic acid or anhydride with polyamine and polyhydricmaterial
NL134315C (fr) * 1962-10-04
DE1271877B (de) * 1963-04-23 1968-07-04 Lubrizol Corp Schmieroel
US3381022A (en) * 1963-04-23 1968-04-30 Lubrizol Corp Polymerized olefin substituted succinic acid esters
NL137371C (fr) * 1963-08-02
US3216936A (en) * 1964-03-02 1965-11-09 Lubrizol Corp Process of preparing lubricant additives
GB1101347A (en) * 1964-06-15 1968-01-31 United Eng Foundry Co Improvements in a rolling mill
NL145565B (nl) * 1965-01-28 1975-04-15 Shell Int Research Werkwijze ter bereiding van een smeermiddelcompositie.
US3574576A (en) * 1965-08-23 1971-04-13 Chevron Res Distillate fuel compositions having a hydrocarbon substituted alkylene polyamine
US3821302A (en) * 1965-10-22 1974-06-28 Exxon Research Engineering Co Olefinic ketone imines and oil compositions containing them
US3272746A (en) * 1965-11-22 1966-09-13 Lubrizol Corp Lubricating composition containing an acylated nitrogen compound
GB1195749A (en) * 1966-12-19 1970-06-24 Lubrizol Corp Sulfur-Containing Cycloaliphatic Reaction Products and their use in Lubricant Compositions
US3519565A (en) * 1967-09-19 1970-07-07 Lubrizol Corp Oil-soluble interpolymers of n-vinylthiopyrrolidones
US3493520A (en) * 1968-06-04 1970-02-03 Sinclair Research Inc Ashless lubricating oil detergents
GB1244435A (en) * 1968-06-18 1971-09-02 Lubrizol Corp Oil-soluble graft polymers derived from degraded ethylene-propylene interpolymers
US3702300A (en) * 1968-12-20 1972-11-07 Lubrizol Corp Lubricant containing nitrogen-containing ester
US3576743A (en) * 1969-04-11 1971-04-27 Lubrizol Corp Lubricant and fuel additives and process for making the additives
US3632511A (en) * 1969-11-10 1972-01-04 Lubrizol Corp Acylated nitrogen-containing compositions processes for their preparationand lubricants and fuels containing the same
US3671511A (en) * 1970-04-23 1972-06-20 Lewis R Honnen Process for preparing polyolefin-substituted amines
US3957855A (en) * 1971-06-11 1976-05-18 The Lubrizol Corporation Ester-containing compositions
US3957854A (en) * 1971-06-11 1976-05-18 The Lubrizol Corporation Ester-containing compositions
US3804763A (en) * 1971-07-01 1974-04-16 Lubrizol Corp Dispersant compositions
US3936480A (en) * 1971-07-08 1976-02-03 Rhone-Progil Additives for improving the dispersing properties of lubricating oil
BE786032A (fr) * 1971-07-08 1973-01-08 Rhone Progil Nouveaux additifs pour huiles lubrifiantes
US3991098A (en) * 1971-11-30 1976-11-09 Toa Nenryo Kogyo Kabushiki Kaisha Lubricating oil additive, process for the synthesis thereof and lubricating oil additive composition
US4071548A (en) * 1971-11-30 1978-01-31 Toa Nenryo Kogyo Kabushiki Kaisha Lubricating oil additive, process for the synthesis thereof and lubricating oil additive composition
US3950341A (en) * 1973-04-12 1976-04-13 Toa Nenryo Kogyo Kabushiki Kaisha Reaction product of a polyalkenyl succinic acid or its anhydride, a hindered alcohol and an amine
US3836471A (en) * 1973-05-14 1974-09-17 Lubrizol Corp Lubricants and fuels containing ester-containing compositions
US4173540A (en) * 1977-10-03 1979-11-06 Exxon Research & Engineering Co. Lubricating oil composition containing a dispersing-varnish inhibiting combination of polyol ester compound and a borated acyl nitrogen compound
US4234435A (en) * 1979-02-23 1980-11-18 The Lubrizol Corporation Novel carboxylic acid acylating agents, derivatives thereof, concentrate and lubricant compositions containing the same, and processes for their preparation
US5652201A (en) * 1991-05-29 1997-07-29 Ethyl Petroleum Additives Inc. Lubricating oil compositions and concentrates and the use thereof
US5763374A (en) * 1994-08-10 1998-06-09 Sanyo Chemical Industries, Ltd. Lubricating oil compositions of reduced high-temperature high-shear viscosity
JP4334623B2 (ja) * 1996-06-12 2009-09-30 出光興産株式会社 自動変速機用潤滑油組成物
US5919109A (en) * 1996-10-16 1999-07-06 Linde Aktiengesellschaft Drive axle with planetary gear
US6613722B1 (en) * 1997-03-07 2003-09-02 Exxon Chemical Patents Inc. Lubricating composition
US6482777B2 (en) * 1998-10-19 2002-11-19 The Lubrizol Corporation Lubricating compositions with improved thermal stability and limited slip performance
DE10215692A1 (de) * 2002-04-10 2003-10-23 Zahnradfabrik Friedrichshafen Antriebsvorrichtung für Tandem-Achsen
US7759294B2 (en) * 2003-10-24 2010-07-20 Afton Chemical Corporation Lubricant compositions
US7452851B2 (en) * 2003-10-24 2008-11-18 Afton Chemical Corporation Lubricant compositions
US7786059B2 (en) * 2004-12-21 2010-08-31 Chevron Oronite Company Llc Anti-wear additive composition and lubricating oil composition containing the same
US20060240998A1 (en) * 2005-04-22 2006-10-26 William Sullivan Corrosion protection for lubricants

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4344854A (en) * 1975-03-21 1982-08-17 The Lubrizol Corporation Sulfurized compositions
US4031023A (en) * 1976-02-19 1977-06-21 The Lubrizol Corporation Lubricating compositions and methods utilizing hydroxy thioethers
US4752416A (en) * 1986-12-11 1988-06-21 The Lubrizol Corporation Phosphite ester compositions, and lubricants and functional fluids containing same
EP0399764A1 (fr) * 1989-05-22 1990-11-28 Ethyl Petroleum Additives Limited Compositions lubrifiantes
EP0646639A1 (fr) * 1993-08-20 1995-04-05 The Lubrizol Corporation Compositions lubrifiantes
EP0695799A2 (fr) * 1994-08-03 1996-02-07 The Lubrizol Corporation Une combination d'un composé de soufre et des composés spécifiques de phosphore et leurs utilisation dans des compositions lubrifiantes, des concentrés et des graisses
WO2000071646A1 (fr) * 1999-05-24 2000-11-30 The Lubrizol Corporation Huiles minerales pour engrenages et liquides a transmissions
US6534451B1 (en) * 2002-04-05 2003-03-18 Infineum International Ltd. Power transmission fluids with improved extreme pressure lubrication characteristics and oxidation resistance
EP1624043A2 (fr) * 2004-07-28 2006-02-08 Afton Chemical Corporation Fluides de transport de force motrice ayant des caractéristiques de pression extrême et d'anti-usure améliorées

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2012087781A1 (fr) * 2010-12-21 2012-06-28 The Lubrizol Corporation Copolymères fonctionnalisés et compositions lubrifiantes à base de ceux-ci
AU2011349666B2 (en) * 2010-12-21 2017-03-09 The Lubrizol Corporation Functionalized copolymers and lubricating compositions thereof
US10035968B2 (en) 2010-12-21 2018-07-31 The Lubrizol Corporation Functionalized copolymers and lubricating compositions thereof
RU2453586C1 (ru) * 2011-03-29 2012-06-20 Государственное образовательное учреждение Высшего профессионального образования Волгоградский государственный технический университет (ВолГТУ) Трасмиссионное масло

Also Published As

Publication number Publication date
CN101100625A (zh) 2008-01-09
CN101100625B (zh) 2012-02-01
US20070270317A1 (en) 2007-11-22

Similar Documents

Publication Publication Date Title
US6451745B1 (en) High boron formulations for fluids continuously variable transmissions
EP1233051B1 (fr) L'utilisé de formulations d'huile de transmission propre à faible teneur en phosphore
US7833955B2 (en) Viscosity modifiers in controlled release lubricant additive gels
EP1499701B2 (fr) Procédé de lubrification d'une transmission a double embrayage
EP1233054A1 (fr) Fluides pour transmissions automatiques avec des caractéristiques anti-vibration ameliorées
CA2967334C (fr) Esters phosphores mixtes pour des applications de lubrifiant
EP0753564A1 (fr) Compositions lubrifiantes pour réduire le bruit dans une transmission continuellement variable du type lien poussant
US20100130390A1 (en) Multifunctional Driveline Fluid
CN102317418A (zh) 无级变速机油组合物
CN101679900A (zh) 包含基于羟基多羧酸衍生物和钼化合物的无灰抗磨剂的润滑组合物
US5547596A (en) Lubricant composition for limited slip differential of car
US20070270317A1 (en) Power Transmission Fluids
US20020151443A1 (en) Automatic transmission fluids with improved anti-wear properties
EP3735455B1 (fr) Huile d'engrenage d'automobile contenant du bore
KR20230129378A (ko) 변속기 유체에서의 마찰 성능 수명 재생 및/또는 연장
US20110111992A1 (en) Lubricating fluids
US20110143982A1 (en) Additive System for Lubricating Fluids
US20070167334A1 (en) Lubricating fluids
US8778855B2 (en) Lubricating oil composition for continuously variable transmissions
WO2021262988A1 (fr) Esters de phosphonate cycliques pour applications de lubrification
KR20240009880A (ko) 몰리브덴을 함유하는 트랜스미션 윤활제
KR20220124257A (ko) 마찰 변형제 화합물 및 관련 조성물 및 방법
KR20230042294A (ko) 자동차 변속기용 윤활제 조성물

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20070509

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LI LT LU LV MC MT NL PL PT RO SE SI SK TR

AX Request for extension of the european patent

Extension state: AL BA HR MK YU

17Q First examination report despatched

Effective date: 20080222

AKX Designation fees paid
RBV Designated contracting states (corrected)

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LI LT LU LV MC MT NL PL PT RO SE SI SK TR

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

18D Application deemed to be withdrawn

Effective date: 20150414