EP3322781A1 - Lubrifiants à base d'un détergent contenant du calcium et leur utilisation pour améliorer un pré-allumage à basse vitesse - Google Patents

Lubrifiants à base d'un détergent contenant du calcium et leur utilisation pour améliorer un pré-allumage à basse vitesse

Info

Publication number
EP3322781A1
EP3322781A1 EP16741792.2A EP16741792A EP3322781A1 EP 3322781 A1 EP3322781 A1 EP 3322781A1 EP 16741792 A EP16741792 A EP 16741792A EP 3322781 A1 EP3322781 A1 EP 3322781A1
Authority
EP
European Patent Office
Prior art keywords
lubricating oil
oil composition
calcium
detergent
low
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
EP16741792.2A
Other languages
German (de)
English (en)
Other versions
EP3322781B1 (fr
Inventor
Kristin FLETCHER
William Y. Lam
Kongsheng Yang
Jeremy Styer
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
Priority claimed from US15/047,934 external-priority patent/US20170015933A1/en
Priority claimed from US15/147,317 external-priority patent/US10336959B2/en
Application filed by Afton Chemical Corp filed Critical Afton Chemical Corp
Publication of EP3322781A1 publication Critical patent/EP3322781A1/fr
Application granted granted Critical
Publication of EP3322781B1 publication Critical patent/EP3322781B1/fr
Active legal-status Critical Current
Anticipated expiration legal-status Critical

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M135/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing sulfur, selenium or tellurium
    • C10M135/08—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing sulfur, selenium or tellurium containing a sulfur-to-oxygen bond
    • C10M135/10—Sulfonic acids or derivatives thereof
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M129/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
    • C10M129/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
    • C10M129/26—Carboxylic acids; Salts thereof
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M159/00—Lubricating compositions characterised by the additive being of unknown or incompletely defined constitution
    • C10M159/12—Reaction products
    • C10M159/20—Reaction mixtures having an excess of neutralising base, e.g. so-called overbasic or highly basic products
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M159/00—Lubricating compositions characterised by the additive being of unknown or incompletely defined constitution
    • C10M159/12—Reaction products
    • C10M159/20—Reaction mixtures having an excess of neutralising base, e.g. so-called overbasic or highly basic products
    • C10M159/24—Reaction mixtures having an excess of neutralising base, e.g. so-called overbasic or highly basic products containing sulfonic radicals
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M169/00—Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
    • C10M169/04—Mixtures of base-materials and additives
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
    • C10M2203/102—Aliphatic fractions
    • C10M2203/1025—Aliphatic fractions used as base material
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
    • C10M2205/028—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers containing aliphatic monomers having more than four carbon atoms
    • C10M2205/0285—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers containing aliphatic monomers having more than four carbon atoms used as base material
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02—Hydroxy compounds
    • C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/027—Neutral salts thereof
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02—Hydroxy compounds
    • C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/028—Overbased salts thereof
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/28—Amides; Imides
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/04—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/04—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
    • C10M2219/042—Sulfate esters
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/04—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
    • C10M2219/044—Sulfonic acids, Derivatives thereof, e.g. neutral salts
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/04—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
    • C10M2219/046—Overbasedsulfonic acid salts
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2227/00—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions
    • C10M2227/06—Organic compounds derived from inorganic acids or metal salts
    • C10M2227/066—Organic compounds derived from inorganic acids or metal salts derived from Mo or W
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2010/00—Metal present as such or in compounds
    • C10N2010/04—Groups 2 or 12
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2010/00—Metal present as such or in compounds
    • C10N2010/12—Groups 6 or 16
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/08—Resistance to extreme temperature
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/10—Inhibition of oxidation, e.g. anti-oxidants
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00—Specified use or application for which the lubricating composition is intended
    • C10N2040/25—Internal-combustion engines
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00—Specified use or application for which the lubricating composition is intended
    • C10N2040/25—Internal-combustion engines
    • C10N2040/255—Gasoline engines

Definitions

  • the disclosure relates to lubricant compositions containing one or more oil soluble additives and the use of such lubricating oil compositions to improve low speed pre- ignition.
  • Turbocharged or supercharged engines may exhibit an abnormal combustion phenomenon known as stochastic pre-ignition or low-speed pre-ignition (or“LSPI”).
  • LSPI is a pre-ignition event that may include very high pressure spikes, early combustion during an inappropriate crank angle, and knock. All of these, individually and in combination, have the potential to cause degradation and/or severe damage to the engine.
  • LSPI events occur only sporadically and in an uncontrolled fashion, it is difficult to identify the causes for this phenomenon and to develop solutions to suppress it.
  • Pre-ignition is a form of combustion that results of ignition of the air-fuel mixture in the combustion chamber prior to the desired ignition of the air-fuel mixture by the igniter.
  • Pre-ignition has typically been a problem during high speed engine operation since heat from operation of the engine may heat a part of the combustion chamber to a sufficient temperature to ignite the air-fuel mixture upon contact. This type of pre-ignition is sometimes referred to as hot-spot pre-ignition.
  • the present disclosure relates to a lubricating oil composition and method of operating a boosted internal combustion engine.
  • the lubricating oil composition includes greater than 50 wt.% of a base oil of lubricating viscosity, at least 0.3 wt.% of an overbased detergent having a total base number (TBN) greater than 225 mg KOH/g, and at least 0.2 wt.% of a low-based/neutral detergent having a TBN less than or equal to 175 mg KOH/g, wherein a total amount of calcium from the overbased and low-based/neutral detergent ranges from greater than 1100 ppm by weight to less than 2400 ppm by weight based on a total weight of the lubricating oil composition.
  • TBN total base number
  • the lubricating oil composition may be effective to reduce low-speed pre-ignition events in the boosted internal combustion engine lubricated with the lubricating oil composition.
  • the disclosure provides a method for reducing low- speed pre-ignition events in a boosted internal combustion engine.
  • the method includes a step of lubricating the boosted internal combustion engine with a lubricating oil composition including greater than 50 wt.% of a base oil of lubricating viscosity, at least 0.3 wt.% of an overbased detergent having a TBN greater than 225 mg KOH/g, and at least 0.2 wt.% of a low-based/neutral detergent having a TBN up to 175 mg KOH/g.
  • a total amount of calcium from the overbased and low-based/neutral detergent ranges from greater than 1100 ppm by weight to less than 2400 ppm by weight based on a total weight of the lubricating oil composition.
  • the boosted internal combustion engine is operated and lubricated with the lubricating oil composition whereby the low-speed pre-ignition events in the engine lubricated with the lubricating oil composition may be reduced.
  • the overbased detergent may include an overbased calcium-containing detergent.
  • the overbased calcium-containing detergent may be selected from an overbased calcium sulfonate detergent and an overbased calcium phenate detergent.
  • the overbased detergent may be a calcium-containing detergent or a mixture of two or more overbased calcium containing detergents.
  • the one or more overbased calcium-containing detergent(s) may provide from about 900 to about 2000 ppm by weight calcium to the lubricating oil composition based on a total weight of the lubricating oil composition.
  • the low-based/neutral detergent may be a calcium containing detergent and the low-based/neutral calcium-containing detergent may be a detergent selected from a calcium sulfonate detergent and a calcium phenate detergent.
  • at least 4 wt.% of the total detergent in the lubricating oil composition may be from a low-based/neutral detergent.
  • the lubricating oil composition may have a total mmol metal (M) to total base number (TBN) ratio ranging from greater than 4.5 to about 10.0 or from greater than 8 to about 10.
  • the reduction of low-speed pre-ignition (LSPI) events may be expressed as a ratio of LSPI events of a test oil relative to LSPI events of a reference oil (hereinafter“the LSPI Ratio”), wherein the reference oil R-1 includes an overbased calcium-containing detergent as the sole detergent in the lubricating oil composition in an amount that provides about 2400 ppm calcium to the lubricating oil composition.
  • the LSPI events may be expressed as LSPI counts during 25,000 engine cycles, wherein the engine is operated at 2000 revolutions per minute (RPM) with a brake mean effective pressure (BMEP) of 18,000 kPA.
  • the base oil may be selected from Group I, Group II, Group III, Group IV, or Group V base oils, and a combination of two or more of the foregoing.
  • the greater than 50 wt.% of base oil is selected from the group consisting of Group II, Group III, Group IV, or Group V base oils, and a combination of two or more of the foregoing, wherein the greater than 50 wt.% of base oil is other than diluent oils that arise from provision of additive components or viscosity index improvers in the composition.
  • the lubricating oil composition may include one or more components selected from friction modifiers, antiwear agents, dispersants, antioxidants, and viscosity index improvers.
  • the engine in operation may generate a brake mean effective pressure level of greater than 1,500 kPa (BMEP) at an engine speed of less than 3000 rotations per minute (rpm) or a BMEP of 1,800 kPa at an engine speed of 2000 rpm.
  • BMEP 1,500 kPa
  • the lubricating oil composition may be effective to pass a TEOST 33 bench oxidation test.
  • the low-based/neutral detergent may include a low-based/neutral calcium-containing detergent and a ratio of ppm calcium by weight provided to the lubricating oil composition by the low-based/neutral calcium- containing detergent to ppm of calcium by weight provided to the lubricating oil composition by the overbased calcium-containing detergent may be from 0.05 to 1.0.
  • the total calcium provided to the lubricating oil composition by the overbased detergent may be from 1100 ppm to 1800 ppm, by weight, based on the total weight of the lubricating oil composition.
  • the total calcium provided to the lubricating oil composition by the low-based/neutral calcium-containing detergent may be from 50 ppm to 1000 ppm, by weight, based on the total weight of the lubricating oil composition
  • the lubricating oil composition may comprise not more than 10 wt.% of a Group IV base oil, a Group V base oil, or a combination thereof. In each of the foregoing embodiments, the lubricating oil compositions comprises less than 5 wt.% of a Group V base oil.
  • the overbased calcium-containing detergent may be an overbased calcium sulfonate detergent.
  • the overbased calcium-containing detergent may optionally exclude overbased calcium salicylate detergents.
  • the lubricating oil composition may optionally exclude any magnesium-containing detergents or the lubricating oil composition may be free of magnesium.
  • the lubricating oil composition may not contain any Group IV base oils.
  • the lubricating oil composition may not contain any Group V base oils.
  • additive package As used herein, the terms “additive package,” “additive concentrate,” “additive composition,”“engine oil additive package,”“engine oil additive concentrate,” “crankcase additive package,” “crankcase additive concentrate,” “motor oil additive package,”“motor oil concentrate,” are considered synonymous, fully interchangeable terminology referring the portion of the lubricating oil composition excluding the greater than 50 wt.% of base oil stock mixture.
  • the additive package may or may not include the viscosity index improver or pour point depressant.
  • the term“overbased” relates to metal salts, such as metal salts of sulfonates, carboxylates, salicylates, and/or phenates, wherein the amount of metal present exceeds the stoichiometric amount.
  • metal salts may have a conversion level in excess of 100% (i.e., they may comprise more than 100% of the theoretical amount of metal needed to convert the acid to its“normal,”“neutral” salt).
  • the expression“metal ratio,” often abbreviated as MR is used to designate the ratio of total chemical equivalents of metal in the overbased salt to chemical equivalents of the metal in a neutral salt according to known chemical reactivity and stoichiometry.
  • the metal ratio is one and in an overbased salt, MR, is greater than one.
  • MR overbased salts
  • the overbased detergent has a TBN of greater than 225 mg KOH/g.
  • the overbased detergent may be a combination of two or more overbased detergents each having a TBN of greater than 225 mg KOH/g.
  • the low-based/neutral detergent has a TBN of up to 175 mg KOH/g.
  • the low-based/neutral detergent may be a combination of two or more low- based and/or neutral detergents each having a TBN up to 175 mg KOH/g.
  • “overbased” may be abbreviated“OB” and in some instances,“low-based/neutral” may be abbreviated“LB/N.”
  • total metal refers to the total metal, metalloid or transition metal in the lubricating oil composition including the metal contributed by the detergent component(s) of the lubricating oil composition.
  • 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 the molecule and having predominantly hydrocarbon character.
  • hydrocarbyl groups include:
  • hydrocarbon substituents that is, aliphatic (e.g., alkyl or alkenyl), alicyclic (e.g., cycloalkyl, cycloalkenyl) substituents, and aromatic-, aliphatic-, and alicyclic- substituted aromatic substituents, as well as cyclic substituents wherein the ring is completed through another portion of the molecule (e.g., two substituents together form an alicyclic moiety);
  • aliphatic e.g., alkyl or alkenyl
  • alicyclic e.g., cycloalkyl, cycloalkenyl
  • aromatic-, aliphatic-, and alicyclic- substituted aromatic substituents as well as cyclic substituents wherein the ring is completed through another portion of the molecule (e.g., two substituents together form an alicyclic moiety);
  • substituted hydrocarbon substituents that is, substituents containing non- hydrocarbon groups which, in the context of this disclosure, do not alter the predominantly hydrocarbon substituent (e.g., halo (especially chloro and fluoro), hydroxy, alkoxy, mercapto, alkylmercapto, nitro, nitroso, amino, alkylamino, and sulfoxy); and (c) hetero substituents, that is, substituents which, while having a predominantly hydrocarbon character, in the context of this disclosure, contain other than carbon in a ring or chain otherwise composed of carbon atoms.
  • halo especially chloro and fluoro
  • Heteroatoms may include sulfur, oxygen, and nitrogen, and encompass substituents such as pyridyl, furyl, thienyl, and imidazolyl.
  • substituents such as pyridyl, furyl, thienyl, and imidazolyl.
  • no more than two, for example, no more than one, non- hydrocarbon substituent will be present for every ten carbon atoms in the hydrocarbyl group; typically, there will be no non-hydrocarbon substituents in the hydrocarbyl group.
  • percent by weight means the percentage the recited component represents to the weight of the entire composition.
  • TBN Total Base Number in mg KOH/g composition as measured by the method of ASTM D2896.
  • alkyl refers to straight, branched, cyclic, and/or substituted saturated chain moieties of from about 1 to about 100 carbon atoms.
  • alkenyl refers to straight, branched, cyclic, and/or substituted unsaturated chain moieties of from about 3 to about 10 carbon atoms.
  • aryl refers to single and multi-ring aromatic compounds that may include alkyl, alkenyl, alkylaryl, amino, hydroxyl, alkoxy, halo substituents, and/or heteroatoms including, but not limited to, nitrogen, oxygen, and sulfur.
  • Lubricants, combinations of components, or individual components of the present description may be suitable for use in various types of internal combustion engines. Suitable engine types may include, but are not limited to heavy duty diesel, passenger car, light duty diesel, medium speed diesel, marine engines, or motorcycle engines.
  • An internal combustion engine may be a diesel fueled engine, a gasoline fueled engine, a natural gas fueled engine, a bio-fueled engine, a mixed diesel/biofuel fueled engine, a mixed gasoline/biofuel fueled engine, an alcohol fueled engine, a mixed gasoline/alcohol fueled engine, a compressed natural gas (CNG) fueled engine, or mixtures thereof.
  • a diesel engine may be a compression ignited engine.
  • a diesel engine may be a compression ignited engine with a spark-ignition assist.
  • a gasoline engine may be a spark-ignited engine.
  • An internal combustion engine may also be used in combination with an electrical or battery source of power.
  • An engine so configured is commonly known as a hybrid engine.
  • the internal combustion engine may be a 2-stroke, 4-stroke, or rotary engine.
  • Suitable internal combustion engines include marine diesel engines (such as inland marine), aviation piston engines, low-load diesel engines, and motorcycle, automobile, locomotive, and truck engines.
  • the internal combustion engine may contain components of one or more of an aluminum-alloy, lead, tin, copper, cast iron, magnesium, ceramics, stainless steel, composites, and/or mixtures thereof.
  • the components may be coated, for example, with a diamond-like carbon coating, a lubricated coating, a phosphorus-containing coating, molybdenum-containing coating, a graphite coating, a nano-particle-containing coating, and/or mixtures thereof.
  • the aluminum-alloy may include aluminum silicates, aluminum oxides, or other ceramic materials. In one embodiment the aluminum-alloy is an aluminum- silicate surface.
  • aluminum alloy is intended to be synonymous with“aluminum composite” and to describe a component or surface comprising aluminum and another component intermixed or reacted on a microscopic or nearly microscopic level, regardless of the detailed structure thereof. This would include any conventional alloys with metals other than aluminum as well as composite or alloy-like structures with non-metallic elements or compounds such with ceramic-like materials.
  • the lubricating oil composition for an internal combustion engine may be suitable for any engine irrespective of the sulfur, phosphorus, or sulfated ash (ASTM D-874) content.
  • the sulfur content of the engine oil lubricant may be about 1 wt% or less, or about 0.8 wt% or less, or about 0.5 wt% or less, or about 0.3 wt% or less, or about 0.2 wt% or less. In one embodiment the sulfur content may be in the range of about 0.001 wt% to about 0.5 wt%, or about 0.01 wt% to about 0.3 wt%.
  • the phosphorus content may be about 0.2 wt% or less, or about 0.1 wt% or less, or about 0.085 wt% or less, or about 0.08 wt% or less, or even about 0.06 wt% or less, about 0.055 wt% or less, or about 0.05 wt% or less. In one embodiment the phosphorus content may be about 50 ppm to about 1000 ppm, or about 325 ppm to about 850 ppm.
  • the total sulfated ash content may be about 2 wt% or less, or about 1.5 wt% or less, or about 1.1 wt% or less, or about 1 wt% or less, or about 0.8 wt% or less, or about 0.5 wt% or less.
  • the sulfated ash content may be about 0.05 wt% to about 0.9 wt%, or about 0.1 wt% or about 0.2 wt% to about 0.45 wt%.
  • the sulfur content may be about 0.4 wt% or less, the phosphorus content may be about 0.08 wt% or less, and the sulfated ash is about 1 wt% or less.
  • the sulfur content may be about 0.3 wt% or less, the phosphorus content is about 0.05 wt% or less, and the sulfated ash may be about 0.8 wt% or less.
  • the lubricating oil composition is an engine oil, wherein the lubricating oil composition may have (i) a sulfur content of about 0.5 wt% or less, (ii) a phosphorus content of about 0.1 wt% or less, and (iii) a sulfated ash content of about 1.5 wt% or less.
  • the lubricating oil composition is suitable for use with engines powered by low sulfur fuels, such as fuels containing about 1 to about 5% sulfur. Highway vehicle fuels contain about 15 ppm sulfur (or about 0.0015% sulfur).
  • the lubricating oil composition is suitable for use with boosted internal combustion engines including turbocharged or supercharged internal combustion engines.
  • lubricants of the present description may be suitable to meet one or more industry specification requirements such as ILSAC GF-3, GF-4, GF-5, GF-6, PC-11, CI-4, CJ-4, ACEA A1/B1, A2/B2, A3/B3, A3/B4, A5/B5, C1, C2, C3, C4, C5, E4/E6/E7/E9, Euro 5/6,Jaso DL-1, Low SAPS, Mid SAPS, or original equipment manufacturer specifications such as DexosTM 1, DexosTM 2, MB-Approval 229.51/229.31, VW 502.00, 503.00/503.01, 504.00, 505.00, 506.00/506.01, 507.00, 508.00, 509.00, BMW Longlife-04, Porsche C30, Peugeot Citro ⁇ n Automobiles B712290, B712296, B712297, B712300, B71 2302, B71 2312, B71 2007, B71 2008, Ford WSS-M2C153
  • a “functional fluid” is a term which encompasses a variety of fluids including but not limited to tractor hydraulic fluids, power transmission fluids including automatic transmission fluids, continuously variable transmission fluids and manual transmission fluids, hydraulic fluids, including tractor hydraulic fluids, some gear oils, power steering fluids, fluids used in wind turbines, compressors, some industrial fluids, and fluids related to power train components. It should be noted that within each of these fluids such as, for example, automatic transmission fluids, there are a variety of different types of fluids due to the various transmissions having different designs which have led to the need for fluids of markedly different functional characteristics. This is contrasted by the term“lubricating fluid” which is not used to generate or transfer power.
  • tractor hydraulic fluids are all- purpose products used for all lubricant applications in a tractor except for lubricating the engine.
  • These lubricating applications may include lubrication of gearboxes, power take-off and clutch(es), rear axles, reduction gears, wet brakes, and hydraulic accessories.
  • a functional fluid is an automatic transmission fluid
  • the automatic transmission fluids must have enough friction for the clutch plates to transfer power.
  • the friction coefficient of fluids has a tendency to decline due to the temperature effects as the fluid heats up during operation. It is important that the tractor hydraulic fluid or automatic transmission fluid maintain its high friction coefficient at elevated temperatures, otherwise brake systems or automatic transmissions may fail. This is not a function of an engine oil.
  • Tractor fluids may combine the performance of engine oils with transmissions, differentials, final-drive planetary gears, wet-brakes, and hydraulic performance. While many of the additives used to formulate a UTTO or a STUO fluid are similar in functionality, they may have deleterious effect if not incorporated properly. For example, some anti-wear and extreme pressure additives used in engine oils can be extremely corrosive to the copper components in hydraulic pumps. Detergents and dispersants used for gasoline or diesel engine performance may be detrimental to wet brake performance. Friction modifiers specific to quiet wet brake noise, may lack the thermal stability required for engine oil performance. Each of these fluids, whether functional, tractor, or lubricating, are designed to meet specific and stringent manufacturer requirements.
  • the present disclosure provides novel lubricating oil blends formulated for use as automotive crankcase lubricants.
  • Embodiments of the present disclosure may provide lubricating oils suitable for crankcase applications and having improvements in the following characteristics: air entrainment, alcohol fuel compatibility, antioxidancy, antiwear performance, biofuel compatibility, foam reducing properties, friction reduction, fuel economy, pre-ignition prevention, rust inhibition, sludge and/or soot dispersability, piston cleanliness, deposit formation, and water tolerance.
  • Engine oils of the present disclosure may be formulated by the addition of one or more additives, as described in detail below, to an appropriate base oil formulation.
  • the additives may be combined with a base oil in the form of an additive package (or concentrate) or, alternatively, may be combined individually with a base oil (or a mixture of both).
  • the fully formulated engine oil may exhibit improved performance properties, based on the additives added and their respective proportions.
  • boosted internal combustion engines of the present disclosure include turbocharged and supercharged internal combustion engines.
  • the boosted internal combustion engines include spark-ignited, direct injection and/or port-fuel injection engines.
  • the spark-ignited internal combustion engines may be gasoline engines.
  • the composition of the invention includes a lubricating oil composition containing a base oil of lubricating viscosity and a particular additive composition.
  • the methods of the present disclosure employ the lubricating oil composition containing the additive composition.
  • the lubricating oil composition may be surprisingly effective for use in reducing low-speed pre-ignition events in a boosted internal combustion engine lubricated with the lubricating oil composition.
  • the disclosure provides a method for reducing low- speed pre-ignition events in a boosted internal combustion engine.
  • the method includes a step of lubricating the boosted internal combustion engine with a lubricating oil composition including greater than 50 wt.% of a base oil of lubricating viscosity, at least 0.3 wt.% of an overbased detergent having a TBN greater than 225 mg KOH/g, and at least 0.2 wt.% of a low-based/neutral detergent having a TBN up to 175 mg KOH/g.
  • a total amount of calcium from the overbased and low-based/neutral detergent ranges from greater than 1100 ppm by weight to less than 2400 ppm by weight based on a total weight of the lubricating oil composition.
  • the boosted internal combustion engine is operated and lubricated with the lubricating oil composition whereby the low-speed pre-ignition events in the engine lubricated with the lubricating oil composition may be reduced.
  • the combustion chamber or cylinder walls of a spark- ignited direct injection engine or port fuel injected internal combustion engine provided with a turbocharger or a supercharger is operated and lubricated with the lubricating oil composition whereby the low-speed pre-ignition events in the engine lubricated with the lubricating oil composition may be reduced.
  • the methods of the present invention may include a step of measuring low speed pre-ignition events of the internal combustion engine lubricated with the lubricating oil.
  • the internal combustion engine the reduction of LSPI events is a 50% or greater reduction, or, more preferably, a 75% or greater reduction and the LSPI events are LSPI counts during 25,000 engine cycles, wherein the engine is operated at 2000 revolutions per minute with brake mean effective pressure of 18,000 kPa.
  • embodiments of the disclosure may provide significant and unexpected improvement in reducing LSPI events while maintaining a relatively high calcium detergent concentration in the lubricating oil composition. Embodiments of the disclosure may also provide unexpected improvement in TEOST 33 test while also reducing LSPI events.
  • the lubricating oil composition may also pass a TEOST 33 test.
  • the lubricating oil composition comprises one or more overbased detergents and one or more low-based/neutral detergents.
  • Suitable detergent substrates include phenates, sulfur containing phenates, sulfonates, calixarates, salixarates, salicylates, carboxylic acids, phosphorus acids, mono- and/or di-thiophosphoric acids, alkyl phenols, sulfur coupled alkyl phenol compounds, or methylene bridged phenols.
  • Suitable detergents and their methods of preparation are described in greater detail in numerous patent publications, including US 7,732,390 and references cited therein.
  • the detergent substrate may be salted with an alkali or alkaline earth metal such as, but not limited to, calcium, magnesium, potassium, sodium, lithium, barium, or mixtures thereof.
  • the detergent is free of barium.
  • a suitable detergent may include alkali or alkaline earth metal salts of petroleum sulfonic acids and long chain mono- or di-alkylarylsulfonic acids with the aryl group being benzyl, tolyl, and xylyl.
  • suitable additional detergents include, but are not limited to, calcium phenates, calcium sulfur containing phenates, calcium sulfonates, calcium calixarates, calcium salixarates, calcium salicylates, calcium carboxylic acids, calcium phosphorus acids, calcium mono- and/or di-thiophosphoric acids, calcium alkyl phenols, calcium sulfur coupled alkyl phenol compounds, calcium methylene bridged phenols, magnesium phenates, magnesium sulfur containing phenates, magnesium sulfonates, magnesium calixarates, magnesium salixarates, magnesium salicylates, magnesium carboxylic acids, magnesium phosphorus acids, magnesium mono- and/or di-thiophosphoric acids, magnesium alkyl phenols, magnesium sulfur coupled alkyl phenol compounds, magnesium methylene bridged phenols, sodium phenates, sodium sulfur containing phenates, sodium sulfonates, sodium calixarates, sodium salixarates, sodium salicylates, sodium carboxylic acids, sodium phosphorus
  • Overbased detergents are well known in the art and may be alkali or alkaline earth metal overbased detergent. Such detergents may be prepared by reacting a metal oxide or metal hydroxide with a substrate and carbon dioxide gas.
  • the substrate is typically an acid, for example, an acid such as an aliphatic substituted sulfonic acid, an aliphatic substituted carboxylic acid, or an aliphatic substituted phenol.
  • the terminology“overbased” relates to metal salts, such as metal salts of sulfonates, carboxylates, and phenates, wherein the amount of metal present exceeds the stoichiometric amount.
  • metal salts may have a conversion level in excess of 100% (i.e., they may comprise more than 100% of the theoretical amount of metal needed to convert the acid to its“normal,”“neutral” salt).
  • the expression“metal ratio,” often abbreviated as MR, is used to designate the ratio of total chemical equivalents of metal in the overbased salt to chemical equivalents of the metal in a neutral salt according to known chemical reactivity and stoichiometry.
  • the metal ratio is one and in an overbased salt, MR, is greater than one.
  • overbased salts are commonly referred to as overbased, hyperbased, or superbased salts and may be salts of organic sulfur acids, carboxylic acids, or phenols.
  • An overbased detergent has a TBN of greater 225 mg KOH/gram, or as further examples, a TBN of about 250 mg KOH/gram or greater, or a TBN of about 300 mg KOH/gram or greater, or a TBN of about 350 mg KOH/gram or greater, or a TBN of about 375 mg KOH/gram or greater, or a TBN of about 400 mg KOH/gram or greater.
  • overbased detergents include, but are not limited to, overbased calcium phenates, overbased calcium sulfur containing phenates, overbased calcium sulfonates, overbased calcium calixarates, overbased calcium salixarates, overbased calcium salicylates, overbased calcium carboxylic acids, overbased calcium phosphorus acids, overbased calcium mono- and/or di-thiophosphoric acids, overbased calcium alkyl phenols, overbased calcium sulfur coupled alkyl phenol compounds, overbased calcium methylene bridged phenols, overbased magnesium phenates, overbased magnesium sulfur containing phenates, overbased magnesium sulfonates, overbased magnesium calixarates, overbased magnesium salixarates, overbased magnesium salicylates, overbased magnesium carboxylic acids, overbased magnesium phosphorus acids, overbased magnesium mono- and/or di-thiophosphoric acids, overbased magnesium alkyl phenols, overbased magnesium sulfur coupled alkyl phenol compounds, or overbased magnesium methylene bridged
  • the overbased detergent may have a metal to substrate ratio of from 1.1:1, or from 2:1, or from 4:1, or from 5:1, or from 7:1, or from 10:1.
  • a detergent is effective at reducing or preventing rust in an engine.
  • the detergent may be present at up to 10 wt%, or about about up to 8 wt%, or up to about 4 wt%, or greater than about 4 wt% to about 8 wt% based on a total weight of the lubricating oil composition.
  • the detergent may be present in an amount to provide from about 1100 to about 3500 ppm metal to the finished fluid. In other embodiments, the detergent may provide from about 1100 to about 3000 ppm of metal, or about 1150 to about 2500 ppm of metal, or about 1200 to about 2400 ppm of metal to the finished fluid.
  • the lubricating oil compositions of the present disclosure include at least one overbased detergent having a TBN of greater than 225 mg KOH/gram and at least one neutral/low-based detergent having a TBN of up to 175 mg KOH/gram.
  • the present disclosure also includes methods of using such lubricating oil compositions in a method or lubricating an engine by lubricating the engine with the lubricating oil composition and operating the engine.
  • the lubricating oil composition of the disclosure has a total amount of calcium from the overbased and low-based/neutral detergent that ranges from greater than 1100 ppm by weight to less than 2400 ppm by weight based on a total weight of the lubricating oil composition.
  • the overbased detergent may be an overbased calcium-containing detergent.
  • the overbased calcium-containing detergent may be selected from an overbased calcium sulfonate detergent, an overbased calcium phenate detergent, and an overbased calcium salicylate detergent.
  • the overbased calcium-containing detergent comprises an overbased calcium sulfonate detergent.
  • the overbased detergent is one or more calcium-containing detergents, preferably the overbased detergent is a calcium sulfonate detergent.
  • the one or more overbased calcium-containing detergents provide from about 900 to about 2400 ppm calcium to the finished fluid.
  • the one or more overbased calcium-containing detergents may be present in an amount to provide from about 900 to about 2000 ppm calcium, or from about 900 to about 1800 ppm calcium, or from about 1100 to 1600 ppm calcium, or from about 1200 to 1500 ppm calcium to the finished fluid.
  • the low-based/neutral detergent has a TBN of up to 175 mg KOH/g, or up to 150 mg KOH/g.
  • the low-based/neutral detergent may include a calcium-containing detergent.
  • the low-based neutral calcium-containing detergent may be selected from a calcium sulfonate detergent, a calcium phenate detergent and a calcium salicylate detergent.
  • the low-based/neutral detergent is a calcium-containing detergent or a mixture of calcium-containing detergents.
  • the low-based/neutral detergent is a calcium sulfonate detergent or a calcium phenate detergent.
  • the low-based/neutral detergent comprises at least 2.5 wt.% of the total detergent in the lubricating oil composition. In some embodiments, at least 4 wt.%, or at least 6 wt.%, or at least 8 wt.%, or at least 10 wt.% or at least 12 wt.% or at least 20 wt.% of the total detergent in the lubricating oil composition is a low-based/neutral detergent which may optionally be a low-based/neutral calcium-containing detergent.
  • the one or more low-based/neutral calcium- containing detergents provide from about 50 to about 1000 ppm calcium by weight to the lubricating oil composition based on a total weight of the lubricating oil composition. In some embodiments, the one or more low-based/neutral calcium-containing detergents provide from 75 to less than 800 ppm, or from 100 to 600 ppm, or from 125 to 500 ppm by weight calcium to the lubricating oil composition based on a total weight of the lubricating oil composition.
  • the lubricating oil composition has a ratio of total millimoles metal (M) to TBN of the lubricating oil composition ranging from greater than 4.5 to about 10.0. In some embodiments the ratio of total millimoles metal (M) to TBN of the lubricating oil composition ranges from greater than 8 to less than 10.0 or from 8 to 9.5 or from 8.1 to 9.0.
  • the ratio of the ppm of calcium, by weight, provided to the lubricating oil composition by the low-based/neutral detergent to the ppm of calcium, by weight, provided to the lubricating oil composition by the overbased calcium detergent is from about 0.01 to about 1, or from about 0.03 to about 0.7, or from about 0.05 to about 0.5, or from about 0.08 to about 0.4.
  • the overbased calcium-containing detergent may be an overbased calcium sulfonate detergent.
  • the overbased calcium-containing detergent may optionally exclude overbased calcium salicylate detergents.
  • the lubricating oil may optionally exclude any magnesium-containing detergents or be free of magnesium.
  • the amount of sodium in the lubricating composition may be limited to not more than 150 ppm of sodium, based on a total weight of the lubricating oil composition.
  • the base oil used in the lubricating oil compositions herein may be selected from any of the base oils in Groups I-V as specified in the American Petroleum Institute (API) Base Oil Interchangeability Guidelines.
  • the five base oil groups are as follows:
  • Groups I, II, and III are mineral oil process stocks.
  • Group IV base oils contain true synthetic molecular species, which are produced by polymerization of olefinically unsaturated hydrocarbons.
  • Many Group V base oils are also true synthetic products and may include diesters, polyol esters, polyalkylene glycols, alkylated aromatics, polyphosphate esters, polyvinyl ethers, and/or polyphenyl ethers, and the like, but may also be naturally occurring oils, such as vegetable oils.
  • Group III base oils are derived from mineral oil, the rigorous processing that these fluids undergo causes their physical properties to be very similar to some true synthetics, such as PAOs. Therefore, oils derived from Group III base oils may be referred to as synthetic fluids in the industry.
  • the base oil used in the disclosed lubricating oil composition may be a mineral oil, animal oil, vegetable oil, synthetic oil, or mixtures thereof. Suitable oils may be derived from hydrocracking, hydrogenation, hydrofinishing, unrefined, refined, and re- refined oils, and mixtures thereof.
  • Unrefined oils are those derived from a natural, mineral, or synthetic source without or with little further purification treatment. Refined oils are similar to the unrefined oils except that they have been treated in one or more purification steps, which may result in the improvement of one or more properties. Examples of suitable purification techniques are solvent extraction, secondary distillation, acid or base extraction, filtration, percolation, and the like. Oils refined to the quality of an edible may or may not be useful. Edible oils may also be called white oils. In some embodiments, lubricating oil compositions are free of edible or white oils.
  • Re-refined oils are also known as reclaimed or reprocessed oils. These oils are obtained similarly to refined oils using the same or similar processes. Often these oils are additionally processed by techniques directed to removal of spent additives and oil breakdown products.
  • Mineral oils may include oils obtained by drilling or from plants and animals or any mixtures thereof.
  • oils may include, but are not limited to, castor oil, lard oil, olive oil, peanut oil, corn oil, soybean oil, and linseed oil, as well as mineral lubricating oils, such as liquid petroleum oils and solvent-treated or acid-treated mineral lubricating oils of the paraffinic, naphthenic or mixed paraffinic-naphthenic types.
  • Such oils may be partially or fully hydrogenated, if desired. Oils derived from coal or shale may also be useful.
  • Useful synthetic lubricating oils may include hydrocarbon oils such as polymerized, oligomerized, or interpolymerized olefins (e.g., polybutylenes, polypropylenes, propylene/isobutylene copolymers); poly(1-hexenes), poly(1-octenes), trimers or oligomers of 1-decene, e.g., poly(1-decenes), such materials being often referred to as ⁇ -olefins, and mixtures thereof; alkyl-benzenes (e.g.
  • dodecylbenzenes dodecylbenzenes, tetradecylbenzenes, dinonylbenzenes, di-(2-ethylhexyl)-benzenes); polyphenyls (e.g., biphenyls, terphenyls, alkylated polyphenyls); diphenyl alkanes, alkylated diphenyl alkanes, alkylated diphenyl ethers and alkylated diphenyl sulfides and the derivatives, analogs and homologs thereof or mixtures thereof.
  • Polyalphaolefins are typically hydrogenated materials.
  • Other synthetic lubricating oils include polyol esters, diesters, liquid esters of phosphorus-containing acids (e.g., tricresyl phosphate, trioctyl phosphate, and the diethyl ester of decane phosphonic acid), or polymeric tetrahydrofurans.
  • Synthetic oils may be produced by Fischer-Tropsch reactions and typically may be hydroisomerized Fischer- Tropsch hydrocarbons or waxes. In one embodiment oils may be prepared by a Fischer- Tropsch gas-to-liquid synthetic procedure as well as other gas-to-liquid oils.
  • the greater than 50 wt.% of base oil included in a lubricating composition may be selected from the group consisting of Group I, Group II, a Group III, a Group IV, a Group V, and a combination of two or more of the foregoing, and wherein the greater than 50 wt.% of base oil is other than base oils that arise from provision of additive components or viscosity index improvers in the composition.
  • the greater than 50 wt.% of base oil included in a lubricating composition may be selected from the group consisting of Group II, a Group III, a Group IV, a Group V, and a combination of two or more of the foregoing, and wherein the greater than 50 wt.% of base oil is other than diluent oils that arise from provision of additive components or viscosity index improvers in the composition.
  • the amount of the oil of lubricating viscosity present may be the balance remaining after subtracting from 100 wt% the sum of the amount of the performance additives inclusive of viscosity index improver(s) and/or pour point depressant(s) and/or other top treat additives.
  • the oil of lubricating viscosity that may be present in a finished fluid may be a major amount, such as greater than about 50 wt%, greater than about 60 wt%, greater than about 70 wt%, greater than about 80 wt%, greater than about 85 wt%, or greater than about 90 wt%.
  • the lubricating oil composition may comprise not more than 10 wt.% of a Group IV base oil, a Group V base oil, or a combination thereof. In each of the foregoing embodiments, the lubricating oil compositions comprises less than 5 wt.% of a Group V base oil. The lubricating oil composition does not contain any Group IV base oils. The lubricating oil composition does not contain any Group V base oils.
  • the lubricating oil composition may also include one or more optional components selected from the various additives set forth below.
  • Antioxidants include one or more optional components selected from the various additives set forth below.
  • the lubricating oil compositions herein also may optionally contain one or more antioxidants.
  • Antioxidant compounds are known and include for example, phenates, phenate sulfides, sulfurized olefins, phosphosulfurized terpenes, sulfurized esters, aromatic amines, alkylated diphenylamines (e.g., nonyl diphenylamine, di-nonyl diphenylamine, octyl diphenylamine, di-octyl diphenylamine), phenyl-alpha-naphthylamines, alkylated phenyl- alpha-naphthylamines, hindered non-aromatic amines, phenols, hindered phenols, oil-soluble molybdenum compounds, macromolecular antioxidants, or mixtures thereof. Antioxidant compounds may be used alone or in combination.
  • the hindered phenol antioxidant may contain a secondary butyl and/or a tertiary butyl group as a sterically hindering group.
  • the phenol group may be further substituted with a hydrocarbyl group and/or a bridging group linking to a second aromatic group.
  • Suitable hindered phenol antioxidants include 2,6-di-tert-butylphenol, 4- methyl-2,6-di-tert-butylphenol, 4-ethyl-2,6-di-tert-butylphenol, 4-propyl-2,6-di-tert- butylphenol or 4-butyl-2,6-di-tert-butylphenol, or 4-dodecyl-2,6-di-tert-butylphenol.
  • the hindered phenol antioxidant may be an ester and may include, e.g., IRGANOXTM L-135 available from BASF or an addition product derived from 2,6-di-tert- butylphenol and an alkyl acrylate, wherein the alkyl group may contain about 1 to about 18, or about 2 to about 12, or about 2 to about 8, or about 2 to about 6, or about 4 carbon atoms.
  • Another commercially available hindered phenol antioxidant may be an ester and may include ETHANOXTM 4716 available from Albemarle Corporation.
  • Useful antioxidants may include diarylamines and high molecular weight phenols.
  • the lubricating oil composition may contain a mixture of a diarylamine and a high molecular weight phenol, such that each antioxidant may be present in an amount sufficient to provide up to about 5%, by weight, based upon the final weight of the lubricating oil composition.
  • the antioxidant may be a mixture of about 0.3 to about 1.5% diarylamine and about 0.4 to about 2.5% high molecular weight phenol, by weight, based upon the final weight of the lubricating oil composition.
  • Suitable olefins that may be sulfurized to form a sulfurized olefin include propylene, butylene, isobutylene, polyisobutylene, pentene, hexene, heptene, octene, nonene, decene, undecene, dodecene, tridecene, tetradecene, pentadecene, hexadecene, heptadecene, octadecene, nonadecene, eicosene or mixtures thereof.
  • hexadecene, heptadecene, octadecene, nonadecene, eicosene or mixtures thereof and their dimers, trimers and tetramers are especially useful olefins.
  • the olefin may be a Diels-Alder adduct of a diene such as 1,3-butadiene and an unsaturated ester, such as, butylacrylate.
  • Another class of sulfurized olefin includes sulfurized fatty acids and their esters.
  • the fatty acids are often obtained from vegetable oil or animal oil and typically contain about 4 to about 22 carbon atoms.
  • suitable fatty acids and their esters include triglycerides, oleic acid, linoleic acid, palmitoleic acid or mixtures thereof.
  • the fatty acids are obtained from lard oil, tall oil, peanut oil, soybean oil, cottonseed oil, sunflower seed oil or mixtures thereof.
  • Fatty acids and/or ester may be mixed with olefins, such as ⁇ -olefins.
  • the one or more antioxidant(s) may be present in ranges about 0 wt% to about 20 wt%, or about 0.1 wt% to about 10 wt%, or about 1 wt% to about 5 wt%, of the lubricating oil composition.
  • Antiwear Agents may be present in ranges about 0 wt% to about 20 wt%, or about 0.1 wt% to about 10 wt%, or about 1 wt% to about 5 wt%, of the lubricating oil composition.
  • the lubricating oil compositions herein also may optionally contain one or more antiwear agents.
  • suitable antiwear agents include, but are not limited to, a metal thiophosphate; a metal dialkyldithiophosphate; a phosphoric acid ester or salt thereof; a phosphate ester(s); a phosphite; a phosphorus-containing carboxylic ester, ether, or amide; a sulfurized olefin; thiocarbamate-containing compounds including, thiocarbamate esters, alkylene-coupled thiocarbamates, and bis(S-alkyldithiocarbamyl)disulfides; and mixtures thereof.
  • a suitable antiwear agent may be a molybdenum dithiocarbamate.
  • the phosphorus containing antiwear agents are more fully described in European Patent 612839.
  • the metal in the dialkyl dithio phosphate salts may be an alkali metal, alkaline earth metal, aluminum, lead, tin, molybdenum, manganese, nickel, copper, titanium, or zinc.
  • a useful antiwear agent may be zinc dialkylthiophosphate.
  • suitable antiwear agents include titanium compounds, tartrates, tartrimides, oil soluble amine salts of phosphorus compounds, sulfurized olefins, phosphites (such as dibutyl phosphite), phosphonates, thiocarbamate-containing compounds, such as thiocarbamate esters, thiocarbamate amides, thiocarbamic ethers, alkylene-coupled thiocarbamates, and bis(S-alkyldithiocarbamyl) disulfides.
  • the tartrate or tartrimide may contain alkyl-ester groups, where the sum of carbon atoms on the alkyl groups may be at least 8.
  • the antiwear agent may in one embodiment include a citrate.
  • the antiwear agent may be present in ranges including about 0 wt% to about 15 wt%, or about 0.01 wt% to about 10 wt%, or about 0.05 wt% to about 5 wt%, or about 0.1 wt% to about 3 wt% of the lubricating oil composition.
  • An antiwear compound may be a zinc dihydrocarbyl dithiophosphate (ZDDP) having a P:Zn ratio of from about 1:0.8 to about 1:1.7.
  • ZDDP zinc dihydrocarbyl dithiophosphate
  • the lubricating oil compositions herein may optionally contain one or more boron-containing compounds.
  • boron-containing compounds include borate esters, borated fatty amines, borated epoxides, borated detergents, and borated dispersants, such as borated succinimide dispersants, as disclosed in U.S. Patent No.5,883,057.
  • the boron-containing compound if present, can be used in an amount sufficient to provide up to about 8 wt%, about 0.01 wt% to about 7 wt%, about 0.05 wt% to about 5 wt%, or about 0.1 wt% to about 3 wt% of the lubricating oil composition.
  • Dispersants if present, can be used in an amount sufficient to provide up to about 8 wt%, about 0.01 wt% to about 7 wt%, about 0.05 wt% to about 5 wt%, or about 0.1 wt% to about 3 wt% of the lubricating oil composition.
  • the lubricating oil composition may optionally further comprise one or more dispersants or mixtures thereof.
  • Dispersants are often known as ashless-type dispersants because, prior to mixing in a lubricating oil composition, they do not contain ash-forming metals and they do not normally contribute any ash when added to a lubricant.
  • Ashless type dispersants are characterized by a polar group attached to a relatively high molecular weight hydrocarbon chain.
  • Typical ashless dispersants include N-substituted long chain alkenyl succinimides.
  • N-substituted long chain alkenyl succinimides include polyisobutylene succinimide with number average molecular weight of the polyisobutylene substituent in the range about 350 to about 50,000, or to about 5,000, or to about 3,000.
  • Succinimide dispersants and their preparation are disclosed, for instance in U.S. Pat. No. 7,897,696 or U.S. Pat. No. 4,234,435.
  • the polyolefin may be prepared from polymerizable monomers containing about 2 to about 16, or about 2 to about 8, or about 2 to about 6 carbon atoms.
  • Succinimide dispersants are typically the imide formed from a polyamine, typically a poly(ethyleneamine).
  • the present disclosure further comprises at least one polyisobutylene succinimide dispersant derived from polyisobutylene with number average molecular weight in the range about 350 to about 50,000, or to about 5000, or to about 3000.
  • the polyisobutylene succinimide may be used alone or in combination with other dispersants.
  • polyisobutylene when included, may have greater than 50 mol%, greater than 60 mol%, greater than 70 mol%, greater than 80 mol%, or greater than 90 mol% content of terminal double bonds.
  • PIB is also referred to as highly reactive PIB (“HR-PIB”).
  • HR-PIB having a number average molecular weight ranging from about 800 to about 5000 is suitable for use in embodiments of the present disclosure.
  • Conventional PIB typically has less than 50 mol%, less than 40 mol%, less than 30 mol%, less than 20 mol%, or less than 10 mol% content of terminal double bonds.
  • An HR-PIB having a number average molecular weight ranging from about 900 to about 3000 may be suitable.
  • Such HR-PIB is commercially available, or can be synthesized by the polymerization of isobutene in the presence of a non-chlorinated catalyst such as boron trifluoride, as described in US Patent No. 4,152,499 to Boerzel, et al. and U.S. Patent No. 5,739,355 to Gateau, et al.
  • HR-PIB may lead to higher conversion rates in the reaction, as well as lower amounts of sediment formation, due to increased reactivity.
  • a suitable method is described in U.S. Patent No.7,897,696.
  • the present disclosure further comprises at least one dispersant derived from polyisobutylene succinic anhydride (“PIBSA”).
  • PIBSA polyisobutylene succinic anhydride
  • the PIBSA may have an average of between about 1.0 and about 2.0 succinic acid moieties per polymer.
  • the % actives of the alkenyl or alkyl succinic anhydride can be determined using a chromatographic technique. This method is described in column 5 and 6 in U.S. Pat. No.5,334,321.
  • the dispersant may be derived from a polyalphaolefin (PAO) succinic anhydride.
  • PAO polyalphaolefin
  • the dispersant may be derived from olefin maleic anhydride copolymer.
  • the dispersant may be described as a poly-PIBSA.
  • the dispersant may be derived from an anhydride which is grafted to an ethylene-propylene copolymer.
  • Mannich bases are materials that are formed by the condensation of a higher molecular weight, alkyl substituted phenol, a polyalkylene polyamine, and an aldehyde such as formaldehyde. Mannich bases are described in more detail in U.S. Patent No.3,634,515.
  • a suitable class of dispersants may be high molecular weight esters or half ester amides.
  • a suitable dispersant may also be post-treated by conventional methods by a reaction with any of a variety of agents. Among these are boron, urea, thiourea, dimercaptothiadiazoles, carbon disulfide, aldehydes, ketones, carboxylic acids, hydrocarbon- substituted succinic anhydrides, maleic anhydride, nitriles, epoxides, carbonates, cyclic carbonates, hindered phenolic esters, and phosphorus compounds. US 7,645,726; US 7,214,649; and US 8,048,831 are incorporated herein by reference in their entireties.
  • both the compounds may be post-treated, or further post-treatment, with a variety of post-treatments designed to improve or impart different properties.
  • post-treatments include those summarized in columns 27-29 of U.S. Pat. No.5,241,003, hereby incorporated by reference.
  • Such treatments include, treatment with:
  • Inorganic phosphorous acids or anhydrates e.g., U.S. Pat. Nos. 3,403,102 and 4,648,980;
  • Organic phosphorous compounds e.g., U.S. Pat. No.3,502,677;
  • Carboxylic acid polycarboxylic acids, anhydrides and/or acid halides (e.g., U.S. Pat. Nos.3,708,522 and 4,948,386);
  • Epoxides, polyepoxides or thioexpoxides e.g., U.S. Pat. Nos. 3,859,318 and 5,026,495.
  • Aldehyde or ketone e.g., U.S. Pat. No.3,458,530
  • Carbon disulfide (e.g., U.S. Pat. No.3,256,185);
  • Glycidol e.g., U.S. Pat. No.4,617,137
  • Urea, thourea or guanidine e.g., U.S. Pat. Nos. 3,312,619; 3,865,813; and British Patent GB 1,065,595
  • Organic sulfonic acid e.g., U.S. Pat. No.3,189,544 and British Patent GB 2,140,811
  • Alkenyl cyanide e.g., U.S. Pat. Nos.3,278,550 and 3,366,569)
  • U.S. Pat. Nos.3,278,550 and 3,366,569 e.g., U.S. Pat. Nos.3,278,550 and 3,366,569
  • Diketene e.g., U.S. Pat. No.3,546,243
  • a diisocyanate (e.g., U.S. Pat. No.3,573,205);
  • Alkane sultone e.g., U.S. Pat. No.3,749,695
  • 1,3-Dicarbonyl Compound e.g., U.S. Pat. No.4,579,675;
  • Cyclic lactone e.g., U.S. Pat. Nos. 4,617,138; 4,645,515; 4,668,246; 4,963,275; and 4,971,711;
  • Cyclic carbonate or thiocarbonate linear monocarbonate or polycarbonate, or chloroformate e.g., U.S. Pat. Nos.4,612,132; 4,647,390; 4,648,886; 4,670,170
  • Nitrogen-containing carboxylic acid e.g., U.S. Pat. 4,971,598 and British Patent GB 2,140,811;
  • Hydroxy-protected chlorodicarbonyloxy compound e.g., U.S. Pat. No.4,614,522
  • Lactam, thiolactam, thiolactone or ditholactone e.g., U.S. Pat. Nos. 4,614,603 and 4,666,460
  • Cyclic carbonate or thiocarbonate, linear monocarbonate or polycarbonate, or chloroformate e.g., U.S. Pat. Nos.4,612,132; 4,647,390; 4,646,886; and 4,670,170
  • Nitrogen-containing carboxylic acid e.g., U.S. Pat. No.4,971,598 and British Patent GB 2,440,811;
  • Hydroxy-protected chlorodicarbonyloxy compound e.g., U.S. Pat. No.4,614,522
  • Lactam, thiolactam, thiolactone or dithiolactone e.g., U.S. Pat. Nos. 4,614,603, and 4,666,460
  • Cyclic carbamate, cyclic thiocarbamate or cyclic dithiocarbamate e.g., U.S. Pat. Nos. 4,663,062 and 4,666,459;
  • Hydroxyaliphatic carboxylic acid e.g., U.S. Pat. Nos. 4,482,464; 4,521,318; 4,713,189;
  • Oxidizing agent e.g., U.S. Pat. No.4,379,064.
  • the TBN of a suitable dispersant may be from about 10 to about 65 on an oil- free basis, which is comparable to about 5 to about 30 TBN if measured on a dispersant sample containing about 50% diluent oil.
  • the dispersant if present, can be used in an amount sufficient to provide up to about 20 wt%, based upon the final weight of the lubricating oil composition.
  • Another amount of the dispersant that can be used may be about 0.1 wt% to about 15 wt%, or about 0.1 wt% to about 10 wt%, or about 3 wt% to about 10 wt%, or about 1 wt% to about 6 wt%, or about 7 wt% to about 12 wt%, based upon the final weight of the lubricating oil composition.
  • the lubricating oil composition utilizes a mixed dispersant system. A single type or a mixture of two or more types of dispersants in any desired ratio may be used. Friction Modifiers
  • the lubricating oil compositions herein also may optionally contain one or more friction modifiers.
  • Suitable friction modifiers may comprise metal containing and metal-free friction modifiers and may include, but are not limited to, imidazolines, amides, amines, succinimides, alkoxylated amines, alkoxylated ether amines, amine oxides, amidoamines, nitriles, betaines, quaternary amines, imines, amine salts, amino guanadine, alkanolamides, phosphonates, metal-containing compounds, glycerol esters, sulfurized fatty compounds and olefins, sunflower oil other naturally occurring plant or animal oils, dicarboxylic acid esters, esters or partial esters of a polyol and one or more aliphatic or aromatic carboxylic acids, and the like.
  • Suitable friction modifiers may contain hydrocarbyl groups that are selected from straight chain, branched chain, or aromatic hydrocarbyl groups or mixtures thereof, and may be saturated or unsaturated.
  • the hydrocarbyl groups may be composed of carbon and hydrogen or hetero atoms such as sulfur or oxygen.
  • the hydrocarbyl groups may range from about 12 to about 25 carbon atoms.
  • the friction modifier may be a long chain fatty acid ester.
  • the long chain fatty acid ester may be a mono-ester, or a di-ester, or a (tri)glyceride.
  • the friction modifier may be a long chain fatty amide, a long chain fatty ester, a long chain fatty epoxide derivatives, or a long chain imidazoline.
  • suitable friction modifiers may include organic, ashless (metal-free), nitrogen-free organic friction modifiers.
  • Such friction modifiers may include esters formed by reacting carboxylic acids and anhydrides with alkanols and generally include a polar terminal group (e.g. carboxyl or hydroxyl) covalently bonded to an oleophilic hydrocarbon chain.
  • An example of an organic ashless nitrogen-free friction modifier is known generally as glycerol monooleate (GMO) which may contain mono-, di-, and tri-esters of oleic acid.
  • GMO glycerol monooleate
  • Other suitable friction modifiers are described in U.S. Pat. No.6,723,685, herein incorporated by reference in its entirety.
  • Aminic friction modifiers may include amines or polyamines. Such compounds can have hydrocarbyl groups that are linear, either saturated or unsaturated, or a mixture thereof and may contain from about 12 to about 25 carbon atoms. Further examples of suitable friction modifiers include alkoxylated amines and alkoxylated ether amines. Such compounds may have hydrocarbyl groups that are linear, either saturated, unsaturated, or a mixture thereof. They may contain from about 12 to about 25 carbon atoms. Examples include ethoxylated amines and ethoxylated ether amines.
  • the amines and amides may be used as such or in the form of an adduct or reaction product with a boron compound such as a boric oxide, boron halide, metaborate, boric acid or a mono-, di- or tri-alkyl borate.
  • a boron compound such as a boric oxide, boron halide, metaborate, boric acid or a mono-, di- or tri-alkyl borate.
  • boron compound such as a boric oxide, boron halide, metaborate, boric acid or a mono-, di- or tri-alkyl borate.
  • a friction modifier may optionally be present in ranges such as about 0 wt% to about 10 wt%, or about 0.01 wt% to about 8 wt%, or about 0.1 wt% to about 4 wt%.
  • the lubricating oil compositions herein also may optionally contain one or more molybdenum-containing compounds.
  • An oil-soluble molybdenum compound may have the functional performance of an antiwear agent, an antioxidant, a friction modifier, or mixtures thereof.
  • An oil-soluble molybdenum compound may include molybdenum dithiocarbamates, molybdenum dialkyldithiophosphates, molybdenum dithiophosphinates, amine salts of molybdenum compounds, molybdenum xanthates, molybdenum thioxanthates, molybdenum sulfides, molybdenum carboxylates, molybdenum alkoxides, a trinuclear organo-molybdenum compound, and/or mixtures thereof.
  • the molybdenum sulfides include molybdenum disulfide.
  • the molybdenum disulfide may be in the form of a stable dispersion.
  • oil-soluble molybdenum compound may be selected from the group consisting of molybdenum dithiocarbamates, molybdenum dialkyldithiophosphates, amine salts of molybdenum compounds, and mixtures thereof. In one embodiment the oil-soluble molybdenum compound may be a molybdenum dithiocarbamate.
  • Suitable examples of molybdenum compounds which may be used include commercial materials sold under the trade names such as Molyvan 822TM, MolyvanTM A, Molyvan 2000TM and Molyvan 855TM from R. T. Vanderbilt Co., Ltd., and Sakura-LubeTM S- 165, S-200, S-300, S-310G, S-525, S-600, S-700, and S-710 available from Adeka Corporation, and mixtures thereof.
  • Suitable molybdenum components are described in US 5,650,381; US RE 37,363 E1; US RE 38,929 E1; and US RE 40,595 E1, incorporated herein by reference in their entireties.
  • the molybdenum compound may be an acidic molybdenum compound. Included are molybdic acid, ammonium molybdate, sodium molybdate, potassium molybdate, and other alkaline metal molybdates and other molybdenum salts, e.g., hydrogen sodium molybdate, MoOCl 4 , MoO 2 Br 2 , Mo 2 O 3 Cl 6 , molybdenum trioxide or similar acidic molybdenum compounds.
  • the compositions can be provided with molybdenum by molybdenum/sulfur complexes of basic nitrogen compounds as described, for example, in U.S. Pat. Nos.
  • organo-molybdenum compounds are trinuclear molybdenum compounds, such as those of the formula Mo 3 S k L n Q z and mixtures thereof, wherein S represents sulfur, L represents independently selected ligands having organo groups with a sufficient number of carbon atoms to render the compound soluble or dispersible in the oil, n is from 1 to 4, k varies from 4 through 7, Q is selected from the group of neutral electron donating compounds such as water, amines, alcohols, phosphines, and ethers, and z ranges from 0 to 5 and includes non-stoichiometric values.
  • S sulfur
  • L represents independently selected ligands having organo groups with a sufficient number of carbon atoms to render the compound soluble or dispersible in the oil
  • n is from 1 to 4
  • k varies from 4 through 7
  • Q is selected from the group of neutral electron donating compounds such as water, amines, alcohols, phosphines, and ethers
  • At least 21 total carbon atoms may be present among all the ligands' organo groups, such as at least 25, at least 30, or at least 35 carbon atoms. Additional suitable molybdenum compounds are described in U.S. Pat. No.6,723,685, herein incorporated by reference in its entirety.
  • the oil-soluble molybdenum compound may be present in an amount sufficient to provide about 0.5 ppm to about 2000 ppm, about 1 ppm to about 700 ppm, about 1 ppm to about 550 ppm, about 5 ppm to about 300 ppm, or about 20 ppm to about 250 ppm of molybdenum. Titanium-containing compounds
  • Another class of additives includes oil-soluble titanium compounds.
  • the oil- soluble titanium compounds may function as antiwear agents, friction modifiers, antioxidants, deposit control additives, or more than one of these functions.
  • the oil soluble titanium compound may be a titanium (IV) alkoxide.
  • the titanium alkoxide may be formed from a monohydric alcohol, a polyol, or mixtures thereof.
  • the monohydric alkoxides may have 2 to 16, or 3 to 10 carbon atoms.
  • the titanium alkoxide may be titanium (IV) isopropoxide.
  • the titanium alkoxide may be titanium (IV) 2-ethylhexoxide.
  • the titanium compound may be the alkoxide of a 1,2-diol or polyol.
  • the 1,2-diol comprises a fatty acid mono-ester of glycerol, such as oleic acid.
  • the oil soluble titanium compound may be a titanium carboxylate.
  • the titanium (IV) carboxylate may be titanium neodecanoate.
  • the oil soluble titanium compound may be present in the lubricating oil composition in an amount to provide from zero to about 1500 ppm titanium by weight or about 10 ppm to 500 ppm titanium by weight or about 25 ppm to about 150 ppm. Transition metal-containing compounds
  • the oil-soluble compound may be a transition metal containing compound or a metalloid.
  • the transition metals may include, but are not limited to, titanium, vanadium, copper, zinc, zirconium, molybdenum, tantalum, tungsten, and the like.
  • Suitable metalloids include, but are not limited to, boron, silicon, antimony, tellurium, and the like.
  • the oil-soluble compound that may be used in a weight ratio of Ca/M ranging from about 0.8:1 to about 70:1 is a titanium containing compound, wherein M is the total metal in the lubricant composition as described above.
  • the titanium- containing compounds may function as antiwear agents, friction modifiers, antioxidants, deposit control additives, or more than one of these functions.
  • titanium containing compounds that may be used in, or which may be used for preparation of the oils- soluble materials of, the disclosed technology are various Ti (IV) compounds such as titanium (IV) oxide; titanium (IV) sulfide; titanium (IV) nitrate; titanium (IV) alkoxides such as titanium methoxide, titanium ethoxide, titanium propoxide, titanium isopropoxide, titanium butoxide, titanium 2-ethylhexoxide; and other titanium compounds or complexes including but not limited to titanium phenates; titanium carboxylates such as titanium (IV) 2- ethyl-1-3-hexanedioate or titanium citrate or titanium oleate; and titanium (IV) (triethanolaminato)isopropoxide.
  • Ti (IV) compounds such as titanium (IV) oxide; titanium (IV) sulfide; titanium (IV) nitrate; titanium (IV) alkoxides such as titanium methoxide, titanium ethoxide, titanium propoxide,
  • titanium phosphates such as titanium dithiophosphates (e.g., dialkyldithiophosphates) and titanium sulfonates (e.g., alkylbenzenesulfonates), or, generally, the reaction product of titanium compounds with various acid materials to form salts, such as oil-soluble salts.
  • Titanium compounds can thus be derived from, among others, organic acids, alcohols, and glycols.
  • Ti compounds may also exist in dimeric or oligomeric form, containing Ti--O--Ti structures.
  • Such titanium materials are commercially available or can be readily prepared by appropriate synthesis techniques which will be apparent to the person skilled in the art. They may exist at room temperature as a solid or a liquid, depending on the particular compound. They may also be provided in a solution form in an appropriate inert solvent.
  • the titanium can be supplied as a Ti-modified dispersant, such as a succinimide dispersant.
  • a Ti-modified dispersant such as a succinimide dispersant.
  • Such materials may be prepared by forming a titanium mixed anhydride between a titanium alkoxide and a hydrocarbyl-substituted succinic anhydride, such as an alkenyl- (or alkyl) succinic anhydride.
  • the resulting titanate-succinate intermediate may be used directly or it may be reacted with any of a number of materials, such as (a) a polyamine-based succinimide/amide dispersant having free, condensable --NH functionality; (b) the components of a polyamine-based succinimide/amide dispersant, i.e., an alkenyl- (or alkyl-) succinic anhydride and a polyamine, (c) a hydroxy-containing polyester dispersant prepared by the reaction of a substituted succinic anhydride with a polyol, aminoalcohol, polyamine, or mixtures thereof.
  • a polyamine-based succinimide/amide dispersant having free, condensable --NH functionality
  • the components of a polyamine-based succinimide/amide dispersant i.e., an alkenyl- (or alkyl-) succinic anhydride and a polyamine
  • a hydroxy-containing polyester dispersant prepared by the
  • the titanate-succinate intermediate may be reacted with other agents such as alcohols, aminoalcohols, ether alcohols, polyether alcohols or polyols, or fatty acids, and the product thereof either used directly to impart Ti to a lubricant, or else further reacted with the succinic dispersants as described above.
  • succinic dispersants as described above.
  • 1 part (by mole) of tetraisopropyl titanate may be reacted with about 2 parts (by mole) of a polyisobutene-substituted succinic anhydride at 140-150° C for 5 to 6 hours to provide a titanium modified dispersant or intermediate.
  • the resulting material (30 g) may be further reacted with a succinimide dispersant from polyisobutene- substituted succinic anhydride and a polyethylenepolyamine mixture (127 grams + diluent oil) at 150° C for 1.5 hours, to produce a titanium-modified succinimide dispersant.
  • a succinimide dispersant from polyisobutene- substituted succinic anhydride and a polyethylenepolyamine mixture (127 grams + diluent oil) at 150° C for 1.5 hours, to produce a titanium-modified succinimide dispersant.
  • Another titanium containing compound may be a reaction product of titanium alkoxide and C6 to C25 carboxylic acid.
  • the reaction product may be represented by the following formula:
  • n is an integer selected from 2, 3 and 4, and R is a hydrocarbyl group containing from about 5 to about 24 carbon atoms, or by the formula:
  • each of R1 , R2 , R3, and R4 are the same or different and are selected from a hydrocarbyl group containing from about 5 to about 25 carbon atoms.
  • Suitable carboxylic acids may include, but are not limited to caproic acid, caprylic acid, lauric acid, myristic acid, palmitic acid, stearic acid, arachidic acid, oleic acid, erucic acid, linoleic acid, linolenic acid, cyclohexanecarboxylic acid, phenylacetic acid, benzoic aicd, neodecanoic acid, and the like.
  • the oil soluble titanium compound may be present in the lubricating oil composition in an amount to provide from 0 to 3000 ppm titanium by weight or 25 to about 1500 ppm titanium by weight or about 35 ppm to 500 ppm titanium by weight or about 50 ppm to about 300 ppm.
  • Viscosity Index Improvers may be present in the lubricating oil composition in an amount to provide from 0 to 3000 ppm titanium by weight or 25 to about 1500 ppm titanium by weight or about 35 ppm to 500 ppm titanium by weight or about 50 ppm to about 300 ppm.
  • the lubricating oil compositions herein also may optionally contain one or more viscosity index improvers.
  • Suitable viscosity index improvers may include polyolefins, olefin copolymers, ethylene/propylene copolymers, polyisobutenes, hydrogenated styrene- isoprene polymers, styrene/maleic ester copolymers, hydrogenated styrene/butadiene copolymers, hydrogenated isoprene polymers, alpha-olefin maleic anhydride copolymers, polymethacrylates, polyacrylates, polyalkyl styrenes, hydrogenated alkenyl aryl conjugated diene copolymers, or mixtures thereof.
  • Viscosity index improvers may include star polymers and suitable examples are described in US Patent No.8,999,905 B2.
  • the lubricating oil compositions herein also may optionally contain one or more dispersant viscosity index improvers in addition to a viscosity index improver or in lieu of a viscosity index improver.
  • Suitable viscosity index improvers may include functionalized polyolefins, for example, ethylene-propylene copolymers that have been functionalized with the reaction product of an acylating agent (such as maleic anhydride) and an amine; polymethacrylates functionalized with an amine, or esterified maleic anhydride-styrene copolymers reacted with an amine.
  • the total amount of viscosity index improver and/or dispersant viscosity index improver may be about 0 wt% to about 20 wt%, about 0.1 wt% to about 15 wt%, about 0.1 wt% to about 12 wt%, or about 0.5 wt% to about 10 wt%, of the lubricating oil composition.
  • Other Optional Additives may be about 0 wt% to about 20 wt%, about 0.1 wt% to about 15 wt%, about 0.1 wt% to about 12 wt%, or about 0.5 wt% to about 10 wt%, of the lubricating oil composition.
  • additives may be selected to perform one or more functions required of a lubricating fluid. Further, one or more of the mentioned additives may be multi-functional and provide functions in addition to or other than the function prescribed herein.
  • a lubricating oil composition according to the present disclosure may optionally comprise other performance additives.
  • the other performance additives may be in addition to specified additives of the present disclosure and/or may comprise one or more of metal deactivators, viscosity index improvers, ashless TBN boosters, friction modifiers, antiwear agents, corrosion inhibitors, rust inhibitors, dispersants, dispersant viscosity index improvers, extreme pressure agents, antioxidants, foam inhibitors, demulsifiers, emulsifiers, pour point depressants, seal swelling agents and mixtures thereof.
  • fully- formulated lubricating oil will contain one or more of these performance additives.
  • Suitable metal deactivators may include derivatives of benzotriazoles (typically tolyltriazole), dimercaptothiadiazole derivatives, 1,2,4-triazoles, benzimidazoles, 2- alkyldithiobenzimidazoles, or 2-alkyldithiobenzothiazoles; foam inhibitors including copolymers of ethyl acrylate and 2-ethylhexylacrylate and optionally vinyl acetate; demulsifiers including trialkyl phosphates, polyethylene glycols, polyethylene oxides, polypropylene oxides and (ethylene oxide-propylene oxide) polymers; pour point depressants including esters of maleic anhydride-styrene, polymethacrylates, polyacrylates or polyacrylamides.
  • benzotriazoles typically tolyltriazole
  • dimercaptothiadiazole derivatives 1,2,4-triazoles
  • benzimidazoles 2- alkyldithiobenzimidazoles, or
  • Suitable foam inhibitors include silicon-based compounds, such as siloxane.
  • Suitable pour point depressants may include a polymethylmethacrylates or mixtures thereof. Pour point depressants may be present in an amount sufficient to provide from about 0 wt% to about 1 wt%, about 0.01 wt% to about 0.5 wt%, or about 0.02 wt% to about 0.04 wt% based upon the final weight of the lubricating oil composition.
  • Suitable rust inhibitors may be a single compound or a mixture of compounds having the property of inhibiting corrosion of ferrous metal surfaces.
  • Non-limiting examples of rust inhibitors useful herein include oil-soluble high molecular weight organic acids, such as 2-ethylhexanoic acid, lauric acid, myristic acid, palmitic acid, oleic acid, linoleic acid, linolenic acid, behenic acid, and cerotic acid, as well as oil-soluble polycarboxylic acids including dimer and trimer acids, such as those produced from tall oil fatty acids, oleic acid, and linoleic acid.
  • oil-soluble high molecular weight organic acids such as 2-ethylhexanoic acid, lauric acid, myristic acid, palmitic acid, oleic acid, linoleic acid, linolenic acid, behenic acid, and cerotic acid
  • oil-soluble polycarboxylic acids including dimer and trim
  • Suitable corrosion inhibitors include long-chain alpha, omega- dicarboxylic acids in the molecular weight range of about 600 to about 3000 and alkenylsuccinic acids in which the alkenyl group contains about 10 or more carbon atoms such as, tetrapropenylsuccinic acid, tetradecenylsuccinic acid, and hexadecenylsuccinic acid.
  • alkenylsuccinic acids include the half esters of alkenyl succinic acids having about 8 to about 24 carbon atoms in the alkenyl group with alcohols such as the polyglycols. The corresponding half amides of such alkenyl succinic acids are also useful.
  • a useful rust inhibitor is a high molecular weight organic acid.
  • an engine oil is devoid of a rust inhibitor.
  • the rust inhibitor if present, can be used in an amount sufficient to provide about 0 wt% to about 5 wt%, about 0.01 wt% to about 3 wt%, about 0.1 wt% to about 2 wt%, based upon the final weight of the lubricating oil composition.
  • crankcase lubricant may include additive components in the ranges listed in the following table. Table 2
  • the percentages of each component above represent the weight percent of each component, based upon the weight of the final lubricating oil composition.
  • the remainder of the lubricating oil composition consists of one or more base oils.
  • Additives used in formulating the compositions described herein may be blended into the base oil individually or in various sub-combinations. However, it may be suitable to blend all of the components concurrently using an additive concentrate (i.e., additives plus a diluent, such as a hydrocarbon solvent). Additives used in formulating the compositions described herein may be blended into the base oil individually or in various sub-combinations. However, it may be suitable to blend all of the components concurrently using an additive concentrate (i.e., additives plus a diluent, such as a hydrocarbon solvent).
  • an additive concentrate i.e., additives plus a diluent, such as a hydrocarbon solvent
  • the present disclosure provides novel lubricating oil blends specifically formulated for use as automotive engine lubricants.
  • Embodiments of the present disclosure may provide lubricating oils suitable for engine applications that provide improvements in one or more of the following characteristics: low-speed pre-ignition events, antioxidancy, antiwear performance, rust inhibition, fuel economy, water tolerance, air entrainment, seal protection, deposit reduction, i.e. passing the TEOST 33 test, and foam reducing properties.
  • Fully formulated lubricants conventionally contain an additive package, referred to herein as a dispersant/inhibitor package or DI package, that will supply the characteristics that are required in the formulations.
  • DI package a dispersant/inhibitor package
  • Suitable DI packages are described for example in U.S. Patent Nos. 5,204,012 and 6,034,040 for example.
  • additives included in the additive package may be dispersants, seal swell agents, antioxidants, foam inhibitors, lubricity agents, rust inhibitors, corrosion inhibitors, demulsifiers, viscosity index improvers, and the like.
  • these components are well known to those skilled in the art and are generally used in conventional amounts with the additives and compositions described herein.
  • Each of the lubricating oil compositions contained a major amount of a base oil, a base conventional dispersant inhibitor (DI) package plus a viscosity index improver(s), wherein the base DI package (less the viscosity index improver) provided about 8 to 12 percent by weight of the lubricating oil composition.
  • the base DI package contained conventional amounts of dispersant(s), antiwear additive(s), antifoam agent(s), and antioxidant(s) as set forth in Table 3 below.
  • the base DI package contained a succinimide dispersant, a borated succinimide dispersant, a molybdenum-containing compound in an amount to deliver about 80 ppm molybdenum to the lubricating oil composition, an organic friction modifier, one or more antioxidants, and one or more antiwear agents (unless specified otherwise).
  • the base DI package was also blended with about 5 to about 10 wt% of one or more viscosity index improvers.
  • Group I base oil was used as a diluent.
  • the major amount of base oil (about 78 to about 87 wt%) was a Group III base oil.
  • the components that were varied are specified in the Tables and discussion of the Examples below. All the values listed are stated as weight percent of the component in the lubricating oil composition (i.e., active ingredient plus diluent oil, if any), unless specified otherwise.
  • LSPI Low Speed Pre-Ignition
  • GDI diesel fuel direct injection
  • One complete LSPI fired engine test consisted of 4 test cycles. Within a single test cycle, two operational stages or segments are repeated in order to generate LSPI events. In stage A, when LSPI is most likely to occur, the engine is operated at about 2000 rpm and about 18,000 kPa brake mean effective pressure (BMEP).
  • BMEP brake mean effective pressure
  • stage B when LSPI is not likely to occur, the engine is operated at about 1500 rpm and about 17,000 kPa BMEP. For each stage, data is collected over 25,000 engine cycles. The structure of a test cycle is as follows: stage A– stage A– stage B– stage B– stage A– stage A. Each stage is separated by an idle period. Because LSPI is statistically significant during stage A, the LSPI event data that was considered in the present examples only included LSPI generated during stage A operation. Thus, for one complete LSPI fired engine test, data was typically generated over a total of 16 stages and was used to evaluate performance of comparative and inventive oils.
  • LSPI events were determined by monitoring peak cylinder pressure ( ⁇ ) and when 2% of the combustible material in the combustion chamber burns (MFB02).
  • the threshold for peak cylinder pressure is calculated for each cylinder and for each stage and is typically 65,000 to 85,000 kPa.
  • the threshold for MFB02 is calculated for each cylinder and for each stage and typically ranges from about 3.0 to about 7.5 Crank Angle Degree (CAD) After Top Dead Center (ATDC).
  • CAD Crank Angle Degree
  • ATDC Top Dead Center
  • An LSPI was recorded when both the PP and MFB02 thresholds were exceeded in a single engine cycle. LSPI events can be reported in many ways.
  • LSPI Ratio was reported as a ratio of the LSPI events of a test oil relative to the LSPI events of Reference Oil“R-1”.
  • R-1 was a lubricating oil composition formulated with the base DI package and an overbased calcium detergent in an amount to provide about 2400 ppm Ca to the lubricating oil composition. More detailed formulation information for reference oil R-1 is given below. Considerable improvement in LSPI is recognized when there is greater than 50% reduction in LSPI events relative to R-1 (an LSPI Ratio of less than 0.5).
  • a further improvement in LSPI is recognized when there is greater than 70% reduction in LSPI events (an LSPI Ratio of less than 0.3), an even further improvement in LSPI is recognized when there is greater than 75% reduction in LSPI events (an LSPI Ratio of less than 0.25), and an even further improvement in LSPI is recognized when there is greater than 80% reduction in LSPI events relative to R-1 (an LSPI Ratio of less than 0.20), and an even further improvement in LSPI is recognized when there is greater than 90% reduction in LSPI events relative to R-1(an LSPI Ratio of less than 0.10).
  • the LSPI Ratio for the R-1 reference oil is thus deemed to be 1.00.
  • the TEOST-33 test is a bench test that may be used to evaluate oxidative degradation and/or thermal coking of engine oil. According to the test, about 100 mL of test oil is used in a 12 cycle/2 hour test. The test results in bulk oxidation of the oil (about 100 grams) on a hollow heated rod (TEOST depositor rod) that will accumulate the deposits over the test period. The test oil flows over the rod at about 0.5 grams per minute while the test piece is cycled 12 times over a temperature ranging from 200-480 °C. The total deposit is the performance parameter measured. The total deposit is the sum of the deposit on the rod and the deposit in the oil which is removed by filtration. The more deposit measured indicates poorer performance of the additive composition. Specifically, a test oil having a weight gain of 30 mg or less passes the TEOST 33 test.
  • TBN measurements given in the tables below were based on ASTM D2896. TBN measurements were used to report mmol total metal:TBN of the fully formulated example fluid in Table 4 below.
  • Reference oils R-1 and R-2, are included as reference oils to demonstrate the current state of the art.
  • Reference oil R-1 was formulated from about 80.7 wt.% of a Group III base oil, 12.1 wt.% of HiTEC® 11150 PCMO Additive Package available from Afton Chemical Corporation and 7.2 wt.% of a 35 SSI ethylene/propylene copolymer viscosity index improver.
  • HiTEC® 11150 passenger car motor oil additive package is an API SN, ILSAC-GF-5, and ACEA A5/B5 qualified DI package.
  • R-1 also showed the following and properties and partial elemental analysis:
  • R-2 contains only calcium-containing detergents at a higher calcium loading than the tested inventive oils.
  • R-1 and R-2 meet all performance requirements for ILSAC GF-5 and, as such, would demonstrate passing performance in the TEOST-33 bench oxidation test.
  • Comparative examples C-1, C-2, C-3, and C-4 are not commercially available fluids but are designed to demonstrate technical problems experienced by one skilled in the art when the detergent system is modified to meet LSPI performance needs.
  • Example I-5 utilizes a low based sodium sulfonate instead of the low based calcium sulfonate used in inventive examples I-1, I-2, I-3, and I-4 and shows that a significant reduction in LSPI Ratio can be obtained using a sodium-containing low-based/neutral detergent instead of a calcium- containing low-based/neutral detergent.
  • LSPI low base or neutral (“LB/N”) calcium detergent (I-1 to I-4)
  • LB/N low base or neutral
  • Inventive Example I-1 passes the TEOST-33 test while delivering a more significant improvement in LSPI events with an almost 81% reduction in the LSPI Ratio relative to R-1.
  • Inventive Examples I-2 and I-3 provide an even greater reduction in the LSPI Ratio without loss of performance in the TEOST-33 test.
  • Example I-4 demonstrates the use of a LB/N calcium phenate in place of the LB/N calcium sulfonate.
  • I-4 also shows a significant improvement in the LSPI Ratio as well as passing TEOST 33 test.
  • the examples presented in Table 4 clearly demonstrate that the amount of calcium from an OB calcium detergent may be maintained at a higher level by adding additional calcium from a LB/N calcium detergent while still passing the TEOST 33 test and ensuring a significant reduction in LSPI Ratio. Further, unexpectedly, the results obtained in the TEOST 33 test may be improved even in the absence of high amounts of OB calcium detergent. In fact, off-setting the OB calcium detergent with LB/N calcium detergent, unexpectedly and surprisingly improved TEOST 33 test while also reducing the LSPI Ratio.
  • the present data shows that off-setting OB Ca sulfonate with LB/N Ca sulfonate in an amount of greater than 8 % LB/N Ca Sulfonate in the total detergent provides an improvement in LSPI while maintaining performance in TEOST 33 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 disclosure 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 disclosure being indicated by the following claims.
  • each component, compound, substituent or parameter disclosed herein is to be interpreted as being disclosed for use alone or in combination with one or more of each and every other component, compound, substituent or parameter disclosed herein.
  • each amount/value or range of amounts/values for each component, compound, substituent or parameter disclosed herein is to be interpreted as also being disclosed in combination with each amount/value or range of amounts/values disclosed for any other component(s), compounds(s), substituent(s) or parameter(s) disclosed herein and that any combination of amounts/values or ranges of amounts/values for two or more component(s), compounds(s), substituent(s) or parameters disclosed herein are thus also disclosed in combination with each other for the purposes of this description.
  • each lower limit of each range disclosed herein is to be interpreted as disclosed in combination with each upper limit of each range and each specific value within each range disclosed herein for the same component, compounds, substituent or parameter.
  • this disclosure to be interpreted as a disclosure of all ranges derived by combining each lower limit of each range with each upper limit of each range or with each specific value within each range, or by combining each upper limit of each range with each specific value within each range.

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Lubricants (AREA)

Abstract

L'invention concerne une composition d'huile lubrifiante et un procédé de fonctionnement d'un moteur à combustion interne suralimenté. La composition d'huile lubrifiante comprend plus de 50 % en poids d'une huile de base, un détergent surbasique ayant un TBN supérieur à 225 mg KOH/g et un détergent neutre/à faible indice de basicité dont l'indice TBN peut atteindre 175 mg KOH/g. Une quantité totale de calcium présent dans le détergent neutre surbasique et à faible indice de basicité est située dans une plage comprise entre une valeur supérieure à 1100 ppm et inférieure à 2400 ppm en poids sur la base du poids total de la composition d'huile lubrifiante. La composition d'huile lubrifiante et le procédé peuvent être efficaces pour réduire des événements de pré-allumage à basse vitesse dans un moteur à combustion interne suralimenté qui est lubrifié au moyen de la composition d'huile lubrifiante par rapport à des compositions d'huile lubrifiante disponibles dans le commerce.
EP16741792.2A 2015-07-16 2016-07-14 Lubrifiants à base d'un détergent contenant du calcium et leur utilisation pour améliorer un pré-allumage à basse vitesse Active EP3322781B1 (fr)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US201562193297P 2015-07-16 2015-07-16
US15/047,934 US20170015933A1 (en) 2015-07-16 2016-02-19 Additives and lubricating oil compositions for improving low speed pre-ignition
US15/147,317 US10336959B2 (en) 2015-07-16 2016-05-05 Lubricants with calcium-containing detergent and their use for improving low speed pre-ignition
PCT/US2016/042220 WO2017011633A1 (fr) 2015-07-16 2016-07-14 Lubrifiants à base d'un détergent contenant du calcium et leur utilisation pour améliorer un pré-allumage à basse vitesse

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CA (1) CA2991769C (fr)
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CA3041927C (fr) * 2017-01-20 2024-03-05 Chevron Oronite Company Llc Compositions d'huile lubrifiante et procede pour empecher ou reduire le preallumage a faible vitesse dans des moteurs a allumage par etincelles a injection directe
WO2019079246A1 (fr) * 2017-10-18 2019-04-25 Shell Oil Company Procédé de réduction du pré-allumage à faible vitesse
CA3101044A1 (fr) * 2018-05-25 2019-11-28 Chevron Oronite Company Llc Procede de prevention ou de reduction de preallumage a faible vitesse dans des moteurs a bougie a injection directe avec un lubrifiant contenant du silane
CN113930274B (zh) * 2020-06-29 2023-06-13 中国石油化工股份有限公司 一种低黏度节能兼顾低速早燃控制性能的发动机油组合物
CN116144418A (zh) * 2023-02-27 2023-05-23 辽宁百特润滑科技有限责任公司 一种汽机油组合物及其制备方法

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CN107922873A (zh) 2018-04-17
RU2018104014A3 (fr) 2019-12-23
KR20180048596A (ko) 2018-05-10
JP2018520240A (ja) 2018-07-26
BR112018000353B1 (pt) 2022-01-18
EP3322781B1 (fr) 2019-12-18
JP6708831B2 (ja) 2020-06-10
RU2720202C2 (ru) 2020-04-27
KR102103653B1 (ko) 2020-04-22
RU2018104014A (ru) 2019-08-02
CA2991769A1 (fr) 2017-01-19
MX2018000152A (es) 2018-03-23
CA2991769C (fr) 2020-07-07
BR112018000353A2 (pt) 2018-09-11
MX371195B (es) 2020-01-22
CN107922873B (zh) 2021-08-27

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