US20040110646A1 - Long life lubricating oil with enhanced oxidation and nitration resistance - Google Patents

Long life lubricating oil with enhanced oxidation and nitration resistance Download PDF

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US20040110646A1
US20040110646A1 US10/683,651 US68365103A US2004110646A1 US 20040110646 A1 US20040110646 A1 US 20040110646A1 US 68365103 A US68365103 A US 68365103A US 2004110646 A1 US2004110646 A1 US 2004110646A1
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Stanley Cartwright
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    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M163/00Lubricating compositions characterised by the additive being a mixture of a compound of unknown or incompletely defined constitution and a non-macromolecular compound, each of these compounds being essential
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02Hydroxy compounds
    • C10M2207/023Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/027Neutral salts thereof
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02Hydroxy compounds
    • C10M2207/023Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/028Overbased salts thereof
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/14Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/144Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings containing hydroxy groups
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/26Overbased carboxylic acid salts
    • C10M2207/262Overbased carboxylic acid salts derived from hydroxy substituted aromatic acids, e.g. salicylates
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/04Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
    • C10M2219/044Sulfonic acids, Derivatives thereof, e.g. neutral salts
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/04Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
    • C10M2219/046Overbasedsulfonic acid salts
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/06Thio-acids; Thiocyanates; Derivatives thereof
    • C10M2219/062Thio-acids; Thiocyanates; Derivatives thereof having carbon-to-sulfur double bonds
    • C10M2219/066Thiocarbamic type compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2227/00Organic 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
    • C10M2227/09Complexes with metals
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2010/00Metal present as such or in compounds
    • C10N2010/02Groups 1 or 11
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2010/00Metal present as such or in compounds
    • C10N2010/04Groups 2 or 12
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2010/00Metal present as such or in compounds
    • C10N2010/12Groups 6 or 16
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/02Pour-point; Viscosity index
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/10Inhibition of oxidation, e.g. anti-oxidants
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/52Base number [TBN]
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/12Gas-turbines

Definitions

  • the present invention relates to lubricating oils, especially gas engine oils, having extended life as evidenced by a reduction in viscosity increase, oxidation and nitration.
  • Gas fired engines are typically used in the oil and gas industry to drive compressors that compress natural gas at well heads and along pipelines. These engines are large, having up to 16 cylinders and often generate between 500 to 3000 HP. The nature of their use requires them to be able to run continuously near full load conditions, shutting down only for maintenance such as for oil changes. Under these operating conditions severe demands are placed on the engine lubricant. Indeed, because the lubricant is subjected to a high temperature environment, the life of the lubricant often is limited by oil oxidation processes. Additionally, natural gas fired engines generate nitrogen oxides (NO X ) that can limit lubricant life by oil nitration processes. Therefore, gas engine operators are constantly seeking gas engine oils that have improved resistance to oxidation and nitration.
  • NO X nitrogen oxides
  • the ash level of the lubricant often is determined by its formulation components, with metal-containing detergents and metallic-containing antiwear additives contributing to the ash level of the lubricant.
  • Gas engine manufacturers specify the appropriate lubricant ash level for correct operation of a given engine.
  • manufacturers of 2-cycle engines often specify use of an ashless oil.
  • Manufacturers of 4-cycle engine may specify low, medium or high ash depending upon the level required for engine cleanliness and durability.
  • additives are used in lubricants to perform numerous functions. For example, some are antioxidants, some are friction modifiers; and some are extreme pressure agents. Indeed some additives perform more than one function. Also as is known in the art additives will lose their effectiveness if they are improperly combined. Therefore, extreme care must be exercised in combining various additives to assure both compatibility and effectiveness. For example, some friction modifiers affect metal surfaces differently than antiwear agents do. When both are present, friction-reducing and antiwear additives may compete for the surface of the metal parts which are subject to lubrication. This competition can produce a lubricant that is less effective than is suggested by the individual properties of the additive components.
  • the components of a gas engine lubricant need to be selected to meet the specified ash level and to provide, among other functions, a high level of oxidation and nitration resistance. Whether selected components and their amounts can be balanced to meet desired specification is not a priori predictable.
  • the present invention relates to a lubricating oil, especially useful as a gas engine oil, comprising a major amount of a base oil of lubricating viscosity; effective amounts of a mixture of neutral and overbased metallic detergents; and, a minor amount of at least one trinuclear molybdenum compound.
  • the lubricant composition of the invention has extended life as evidenced by reductions in oxidation and nitration relative to commercial and reference oils and may also be compatible with other standard additives used in formulating commercial lubricating compositions.
  • the lubricant compositions of the present invention include a major amount of a base oil of lubricating viscosity.
  • Suitable base oils include natural and synthetic oils and mixtures thereof in API Categories I, II and III, and having a kinematic viscosity of about 9 to 13 cSt at 100° C.
  • the metallic detergent contained in the composition of the invention is a mixture of neutral and overbased metal sulfonates, phenates and alkylsalicylates.
  • the metals may be alkali and alkaline earth metals and preferably are alkaline earth metals, especially calcium and barium.
  • suitable neutral metallic detergents are calcium sulfonates and calcium alkylsalicylates having a TBN of from 10 to 100.
  • overbased metallic detergents are calcium phenates, sulphonates and alkylsalicylates having a TBN of 150 to 400.
  • the amount of the neutral and overbased metallic detergent is chosen having regard to the desired TBN of the final product and especially having regard to the desired sulfated ash of the final product.
  • the mixture of neutral and overbased metallic detergents is sufficient to provide the composition with a sulfated ash in the range of about 0.2 mass % to about 2.0 mass %.
  • compositions of the present invention also include a minor amount of at least one trinuclear molybdenum compound.
  • a preferred trinuclear molybdenum compound is represented by the formula Mo 3 S k L n Q z where L represents independently selected ligands, n varies from 1 to 4, k varies from 4 to 7 and Q is selected from the group consisting of neutral electron donating compounds including water, amines, alcohols, phosphines and ethers and z ranges from 0 to 5.
  • L represents independently selected ligands
  • n varies from 1 to 4
  • Q is selected from the group consisting of neutral electron donating compounds including water, amines, alcohols, phosphines and ethers and z ranges from 0 to 5.
  • Such compounds and their method of preparation are disclosed in great detail in U.S. Pat. No. 6,232,276 B1 which is incorporated herein by reference.
  • L preferably is dithiocarbamate, n is 4, k is 7, Q is an electron-donating compound, and z is 0.
  • the trinuclear molybdenum compound preferably constitutes from 0.1 vol % to about 2.0 vol % based on the total volume of the total lubricant composition.
  • the composition may contain an ashless dihydrocarbyl thiocarbamoyl in combination with the trinuclear molybdenum compound.
  • Suitable dihydrocarbylthiocarbamoyl compounds are represented by the formula
  • R 1 , R 2 , R 3 and R 4 are the same or different and each represents an alkyl group of — 3_ to — 30_ carbon atoms
  • X represents S, S—S, S ⁇ CH 2 ⁇ y S, S—CH 2 CH 2 (CH 3 )—S and y is an integer of 1 to 3.
  • the combined materials will constitute from about 0.1 vol % to about 2.0 vol % based on the volume of the total lubricant composition; however, the amount of dihydrocarbyl thiocarbamoyl will not exceed about 1.90 vol %.
  • the fully formulated oil may contain additional, typical additives known to those skilled in the industry, used on an as-received basis.
  • the fully formulated oil may contain dispersants of the type generally represented by succimides (e.g., polyisobutylene succinic acid/anhydride (PIBSA)-polyamine having a PIB moiety molecular weight of about 700 to 2500).
  • the dispersants may be borated or non-borated.
  • the dispersant can be present in the amount of about 0.5 to 8 vol %, more preferably in the amount of about 1 to 6 vol %, most preferably in the amount of about 2 to 4 vol %.
  • Antioxidants may be of the phenol (e.g., o,o'ditertiary alkyl phenol such as ditertbutyl phenol), or amine (e.g., dialkyl diphenyl amine such as dibutyl, octyl buty, or dioctyl diphenyl amine) type, or mixtures thereof. More preferably, the antioxidants will be hindered phenols, or aryl amines which may or may not be sulfurized. Antioxidants can be present in the amount of about 0.05 to 2.0 vol %, more preferably in the amount of about 0.1 to 1.75 vol %, most preferably in the amount of about 0.5 to 1.5 vol %.
  • phenol e.g., o,o'ditertiary alkyl phenol such as ditertbutyl phenol
  • amine e.g., dialkyl diphenyl amine such as dibutyl, octyl buty, or dioc
  • Metal deactivators may be of the aryl thiazines, triazoles, or alkyl substituted dimercapto thiadiazoles (DMTD's), or mixtures thereof. Metal deactivators can be present in the amount of about 0.01 to 0.2 vol %, more preferably in the amount of about 0.02 to 0.15 vol %, most preferably in the amount of about 0.05 to 0.1 vol %.
  • Antiwear additives such as metal dithiophosphates (e.g., zinc dialkyl dithiophosphate, ZDDP), metal dithiocarbamates, metal xanthates or tricreeylphosphates may be included.
  • Antiwear additives can be present in the amount of about 0.05 to 1.5 vol %, more preferably in the amount of about 0.1 to 1.0 vol %, most preferably in the amount of about 0.2 to 0.5 vol %.
  • Pour point depressants such as poly(meth)acrylates, or alkyl-aromatic polymers may be included. Pour point depressants can be present in the amount of about 0.05 to 0.6 vol %, more preferably in the amount of about 0. 1 to 0.4 vol %, most preferably in the amount of about 0.2 to 0.3 vol %.
  • Antifoamants such as silicone antifoaming agents can be present in the amount of about 0.001 to 0.2 vol %, more preferably in the amount of about 0.005 to 0.15 vol %, most preferably in the amount of about 0.01 to 0.1 vol %.
  • Viscosity index Improvers may be any polymer which imparts multifunctional viscosity properties to the finished oil, including materials such as olefin copolymers, polymethacrylates, styrene diene block copolymers, and star copolymers. the VII's may also be multifunctional from the perspective of offering secondary lubricant performance features such as additional dispersancy. VII's can be present in the amount of up to 15 vol %, more preferably in the amount of up to 13 vol %, most preferably in the amount of up to 10 vol %.
  • Lubricating oil additives are described generally in “Lubricants and Related Products” by Dieter Klamanm, Verlag Chemie, Deerfield, Fla., 1984, and also in “Lubricant Additives” by C. V. Smalheer and R. Kennedy Smith, 1967, pages 1-11, the disclosures of which are incorporated herein by reference.
  • a lab nitration screener test was used to assess the oil life performance of various oil compositions.
  • the test results identify a number of parameters including oil viscosity increase, oxidation, and nitration. All measurements are reported on a relative basis (unless otherwise indicated) so that results greater than unity represent greater levels of degradation. Numerically lower relative results represent a measure of longer oil life.
  • a Reference Oil is tested and results are reported as a ratio of the result for the test oil divided by the result for the Reference Oil. Thus, if a tested oil has an oxidation result of 1.0, then it has oxidation performance equal to that of the Reference Oil. If the tested oil has an oxidation result less than 1.0, then the tested oil demonstrates oxidation performance superior to that of the Reference Oil
  • Comparative Oil 1 was a heavy Group II basestock. Comparative Oil 1, Reference Oil 1 and Examples 1 and 2 contained the same viscosity index improver (VI). Comparative Oil 2 is a current commercial oil based solely on API Group II basestocks. Reference Oil 1 and Example Oils 1 and 2 each contained the same mixture of neutral and overbased metallic detergents, ashless dispersant, ZDDP, pour point depressant, metal passivator and antifoamant.
  • Reference Oil 1 employed a phenolic antioxidant whereas the oils of Examples 1 and 2 employed a trinuclear molybdenum compound, MO 3 S 7 (DTC) 4 , and a mixture of a trinuclear molybdenum compound, MO 3 S 7 (DTC) 4 , and an ashless dihydrocarbyl thiocarbamoyl, (S 2 CNR 2 ) 2 CH 2 , respectively.
  • Comparative Oil 1 used a commercially available gas engine oil additive package, Oloa 1255 sold by Chevron Chemical Company. Oloa 1255 is one of the most widely sold gas engine oil packages and therefore represents a “benchmark standard” against which other engine oil formulations may be measured.

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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

A long life lubricating oil, as evidenced by a reduction in oil thickening, oxidation and nitration, comprises a major amount of a base oil of lubricating viscosity and a minor amount of a mixture of neutral and overbased metallic detergents and at least one trinuclear molybdenum compound.

Description

    CROSS-REFERENCE TO RELATED APPLICATION(S)
  • Non-Provisional Application based on Provisional Application No. 60/419,745 filed Oct. 18, 2002. [0001]
  • This application claims the benefit of U.S. Provisional Application No. 60/419,745 filed Oct. 18, 2002.[0002]
  • FIELD OF INVENTION
  • The present invention relates to lubricating oils, especially gas engine oils, having extended life as evidenced by a reduction in viscosity increase, oxidation and nitration. [0003]
  • BACKGROUND OF INVENTION
  • Gas fired engines are typically used in the oil and gas industry to drive compressors that compress natural gas at well heads and along pipelines. These engines are large, having up to 16 cylinders and often generate between 500 to 3000 HP. The nature of their use requires them to be able to run continuously near full load conditions, shutting down only for maintenance such as for oil changes. Under these operating conditions severe demands are placed on the engine lubricant. Indeed, because the lubricant is subjected to a high temperature environment, the life of the lubricant often is limited by oil oxidation processes. Additionally, natural gas fired engines generate nitrogen oxides (NO[0004] X) that can limit lubricant life by oil nitration processes. Therefore, gas engine operators are constantly seeking gas engine oils that have improved resistance to oxidation and nitration.
  • In addition to controlling oxidation and nitration properties of a gas engine oil it also is necessary to control the ash content of the oil because the lubricant ash acts as a solid lubricant protecting the valve/seat interface of the engine. For this reason gas engine oils are classified according to their ash content. The classifications are: [0005]
    Ash Designation Ash Level, wt % (ASTM D874)
    Ashless Ash < 0.1%
    Low Ash 0.1% < Ash < 0.6%
    Medium Ash 0.6% < Ash < 1.5%
    High Ash Ash > 1.5%
  • The ash level of the lubricant often is determined by its formulation components, with metal-containing detergents and metallic-containing antiwear additives contributing to the ash level of the lubricant. Gas engine manufacturers specify the appropriate lubricant ash level for correct operation of a given engine. Thus, manufacturers of 2-cycle engines often specify use of an ashless oil. Manufacturers of 4-cycle engine may specify low, medium or high ash depending upon the level required for engine cleanliness and durability. [0006]
  • As is known in the art, additives are used in lubricants to perform numerous functions. For example, some are antioxidants, some are friction modifiers; and some are extreme pressure agents. Indeed some additives perform more than one function. Also as is known in the art additives will lose their effectiveness if they are improperly combined. Therefore, extreme care must be exercised in combining various additives to assure both compatibility and effectiveness. For example, some friction modifiers affect metal surfaces differently than antiwear agents do. When both are present, friction-reducing and antiwear additives may compete for the surface of the metal parts which are subject to lubrication. This competition can produce a lubricant that is less effective than is suggested by the individual properties of the additive components. [0007]
  • Accordingly, the components of a gas engine lubricant need to be selected to meet the specified ash level and to provide, among other functions, a high level of oxidation and nitration resistance. Whether selected components and their amounts can be balanced to meet desired specification is not a priori predictable. [0008]
  • SUMMARY OF INVENTION
  • Simply stated the present invention relates to a lubricating oil, especially useful as a gas engine oil, comprising a major amount of a base oil of lubricating viscosity; effective amounts of a mixture of neutral and overbased metallic detergents; and, a minor amount of at least one trinuclear molybdenum compound. [0009]
  • The lubricant composition of the invention has extended life as evidenced by reductions in oxidation and nitration relative to commercial and reference oils and may also be compatible with other standard additives used in formulating commercial lubricating compositions. [0010]
  • DETAILED DESCRIPTION OF INVENTION
  • The lubricant compositions of the present invention include a major amount of a base oil of lubricating viscosity. Suitable base oils include natural and synthetic oils and mixtures thereof in API Categories I, II and III, and having a kinematic viscosity of about 9 to 13 cSt at 100° C. [0011]
  • The metallic detergent contained in the composition of the invention is a mixture of neutral and overbased metal sulfonates, phenates and alkylsalicylates. The metals may be alkali and alkaline earth metals and preferably are alkaline earth metals, especially calcium and barium. Examples of suitable neutral metallic detergents are calcium sulfonates and calcium alkylsalicylates having a TBN of from 10 to 100. Examples of overbased metallic detergents are calcium phenates, sulphonates and alkylsalicylates having a TBN of 150 to 400. The amount of the neutral and overbased metallic detergent is chosen having regard to the desired TBN of the final product and especially having regard to the desired sulfated ash of the final product. Preferably the mixture of neutral and overbased metallic detergents is sufficient to provide the composition with a sulfated ash in the range of about 0.2 mass % to about 2.0 mass %. [0012]
  • The compositions of the present invention also include a minor amount of at least one trinuclear molybdenum compound. A preferred trinuclear molybdenum compound is represented by the formula Mo[0013] 3SkLnQz where L represents independently selected ligands, n varies from 1 to 4, k varies from 4 to 7 and Q is selected from the group consisting of neutral electron donating compounds including water, amines, alcohols, phosphines and ethers and z ranges from 0 to 5. Such compounds and their method of preparation are disclosed in great detail in U.S. Pat. No. 6,232,276 B1 which is incorporated herein by reference. In the present invention L preferably is dithiocarbamate, n is 4, k is 7, Q is an electron-donating compound, and z is 0. The trinuclear molybdenum compound preferably constitutes from 0.1 vol % to about 2.0 vol % based on the total volume of the total lubricant composition.
  • Optionally, the composition may contain an ashless dihydrocarbyl thiocarbamoyl in combination with the trinuclear molybdenum compound. [0014]
  • Suitable dihydrocarbylthiocarbamoyl compounds are represented by the formula [0015]
    Figure US20040110646A1-20040610-C00001
  • where R[0016] 1, R2, R3 and R4 are the same or different and each represents an alkyl group of 3_ to 30_ carbon atoms, X represents S, S—S, SCH2yS, S—CH2CH2(CH3)—S and y is an integer of 1 to 3.
  • Preferably the combined materials will constitute from about 0.1 vol % to about 2.0 vol % based on the volume of the total lubricant composition; however, the amount of dihydrocarbyl thiocarbamoyl will not exceed about 1.90 vol %. [0017]
  • The fully formulated oil may contain additional, typical additives known to those skilled in the industry, used on an as-received basis. [0018]
  • Thus, the fully formulated oil may contain dispersants of the type generally represented by succimides (e.g., polyisobutylene succinic acid/anhydride (PIBSA)-polyamine having a PIB moiety molecular weight of about 700 to 2500). The dispersants may be borated or non-borated. The dispersant can be present in the amount of about 0.5 to 8 vol %, more preferably in the amount of about 1 to 6 vol %, most preferably in the amount of about 2 to 4 vol %. [0019]
  • Antioxidants may be of the phenol (e.g., o,o'ditertiary alkyl phenol such as ditertbutyl phenol), or amine (e.g., dialkyl diphenyl amine such as dibutyl, octyl buty, or dioctyl diphenyl amine) type, or mixtures thereof. More preferably, the antioxidants will be hindered phenols, or aryl amines which may or may not be sulfurized. Antioxidants can be present in the amount of about 0.05 to 2.0 vol %, more preferably in the amount of about 0.1 to 1.75 vol %, most preferably in the amount of about 0.5 to 1.5 vol %. [0020]
  • Metal deactivators may be of the aryl thiazines, triazoles, or alkyl substituted dimercapto thiadiazoles (DMTD's), or mixtures thereof. Metal deactivators can be present in the amount of about 0.01 to 0.2 vol %, more preferably in the amount of about 0.02 to 0.15 vol %, most preferably in the amount of about 0.05 to 0.1 vol %. [0021]
  • Antiwear additives such as metal dithiophosphates (e.g., zinc dialkyl dithiophosphate, ZDDP), metal dithiocarbamates, metal xanthates or tricreeylphosphates may be included. Antiwear additives can be present in the amount of about 0.05 to 1.5 vol %, more preferably in the amount of about 0.1 to 1.0 vol %, most preferably in the amount of about 0.2 to 0.5 vol %. [0022]
  • Pour point depressants such as poly(meth)acrylates, or alkyl-aromatic polymers may be included. Pour point depressants can be present in the amount of about 0.05 to 0.6 vol %, more preferably in the amount of about 0. 1 to 0.4 vol %, most preferably in the amount of about 0.2 to 0.3 vol %. [0023]
  • Antifoamants such as silicone antifoaming agents can be present in the amount of about 0.001 to 0.2 vol %, more preferably in the amount of about 0.005 to 0.15 vol %, most preferably in the amount of about 0.01 to 0.1 vol %. [0024]
  • Viscosity index Improvers (VII's) may be any polymer which imparts multifunctional viscosity properties to the finished oil, including materials such as olefin copolymers, polymethacrylates, styrene diene block copolymers, and star copolymers. the VII's may also be multifunctional from the perspective of offering secondary lubricant performance features such as additional dispersancy. VII's can be present in the amount of up to 15 vol %, more preferably in the amount of up to 13 vol %, most preferably in the amount of up to 10 vol %. [0025]
  • Lubricating oil additives are described generally in “Lubricants and Related Products” by Dieter Klamanm, Verlag Chemie, Deerfield, Fla., 1984, and also in “Lubricant Additives” by C. V. Smalheer and R. Kennedy Smith, 1967, pages 1-11, the disclosures of which are incorporated herein by reference. [0026]
  • The present invention is further described in the following non-limiting examples and comparative examples. [0027]
  • EXPERIMENTAL A. Lab Nitration Screener Test Results
  • A lab nitration screener test was used to assess the oil life performance of various oil compositions. The test results identify a number of parameters including oil viscosity increase, oxidation, and nitration. All measurements are reported on a relative basis (unless otherwise indicated) so that results greater than unity represent greater levels of degradation. Numerically lower relative results represent a measure of longer oil life. In each test, a Reference Oil is tested and results are reported as a ratio of the result for the test oil divided by the result for the Reference Oil. Thus, if a tested oil has an oxidation result of 1.0, then it has oxidation performance equal to that of the Reference Oil. If the tested oil has an oxidation result less than 1.0, then the tested oil demonstrates oxidation performance superior to that of the Reference Oil [0028]
  • EXAMPLES AND COMPARATIVE EXAMPLES
  • In the Examples, the base oil in all cases was a heavy Group II basestock. Comparative Oil 1, Reference Oil 1 and Examples 1 and 2 contained the same viscosity index improver (VI). Comparative Oil 2 is a current commercial oil based solely on API Group II basestocks. Reference Oil 1 and Example Oils 1 and 2 each contained the same mixture of neutral and overbased metallic detergents, ashless dispersant, ZDDP, pour point depressant, metal passivator and antifoamant. Reference Oil 1, however, employed a phenolic antioxidant whereas the oils of Examples 1 and 2 employed a trinuclear molybdenum compound, MO[0029] 3S7(DTC)4, and a mixture of a trinuclear molybdenum compound, MO3S7(DTC)4, and an ashless dihydrocarbyl thiocarbamoyl, (S2CNR2)2CH2, respectively. Comparative Oil 1 used a commercially available gas engine oil additive package, Oloa 1255 sold by Chevron Chemical Company. Oloa 1255 is one of the most widely sold gas engine oil packages and therefore represents a “benchmark standard” against which other engine oil formulations may be measured.
  • The results show that the oils of the present invention, Examples 1 and 2, provided superior performance to both of the Comparative oils and the Reference Oil, in terms of reduced oxidation, nitration and viscosity increase. The invention examples provided superior oil life despite the absence of conventional aminic and phenolic antioxidants. The small negative normalized viscosity increase values for the invention examples simply reflect that there was no significant change in viscosity, unlike the Comparative and Reference oils. [0030]
    TABLE 1
    Comparative Reference Example Example Comparative
    Oil 1 Oil 1 1 2 Oi1 2
    Component (vol %)
    Group II basestock 87.90 90.00 90.00 90.00
    NGEO commercial 9.6
    additive package
    VI
    Phenolic antioxidant 1.00 1.00
    Moly trimer 1.00 1.00
    Ashless dihydrocarbyl 0.50
    thiocarbamoyl
    Balance of additives 1.00 9.00 9.00 9.00
    Commercial Oil 100.00
    Properties
    KV, cSt @ 100° C. 13.25 13.14 13.20 13.13 13.51
    Test Results
    Nitration Screener Test
    Oxidation (relative) 1.76 1.00 0.86 0.79 1.57
    Nitration (relative) 1.55 1.00 1.15 0.91 1.48
    Viscosity Increase 1.70 1.00 −0.16 −0.12 0.73
    (relative)

Claims (10)

What is claimed is:
1. A lubricating composition comprising:
a major amount of an oil of lubricating viscosity;
a mixture of neutral and overbased metallic detergents; and
a minor amount of at least one trinuclear molybdenum compound.
2. The composition of claim 1 wherein the trinuclear molybdenum compound is represented by the formula Mo3SkLnQz where L is an independently selected ligand, n is from 1 to 4, k is from 4 to 7, Q is a neutral electron donating moiety and z is from 0 to 5.
3. The composition of claim 2 wherein the neutral and overbased metallic detergents are selected from the group consisting of alkali and alkaline earth metal sulfonates, phenates, alkylsalicylates and mixtures thereof.
4. The composition of claim 3 wherein the amount of detergents is sufficient to provide the composition with a sulfated ash content in the range of about 0.2 wt % to about 2.0 wt %.
5. The composition of claim 4 wherein the trinuclear molybdenum compound constitutes from about 0.1 vol % to about 2.0 vol % based on the volume of the total lubricant composition.
6. The composition of claim 5 including a minor amount of a dihydrocarbyl thiocarbamoyl compound.
7. The composition of claim 6 wherein the dihydrocarbyl thiocarbamoyl compound has the formula
Figure US20040110646A1-20040610-C00002
where R1, R2, R3 and R4 are the same or different alkyl groups of from 3 to 30 carbon atoms; X is S, S—S, SCH2yS, S—CH2CH2(CH3)—S; and y is an integer of 1 to 3.
8. A lubricating oil composition comprising:
a major amount of an oil of lubricating viscosity;
a mixture of neutral and overbased metallic detergents selected from the group consisting essentially of alkaline earth metal sulfonates, phenates, alkylsalicylates and mixtures thereof in an amount sufficient to provide the composition with a sulfated ash content of from about 0.2 wt % to about 2.0 wt %;
a trinuclear molybdenum compound having the formula
Mo3SkLnQz
where L is an independently selected ligand, n is from 1 to 4, k is from 4 to 7, Q is a neutral electron donating moiety, and z is from 0 to 5;
from 0 to 2.0 vol % of a dihydrocarbyl thiocarbamoyl compound having the formula;
Figure US20040110646A1-20040610-C00003
where R1, R2, R3 and R4 are the same or different alkyl groups of from 3 to 30 carbon atoms; X is S, S—S, SCH2yS, S—CH2CH2(CH3)—S; and y is an integer of 1 to 3;
the amount of trinuclear molybdenum compound and dihydrocarbyl thiocarbomyl compound being in the range of about 0.1 vol % to about 2.0 vol %.
9. A method for enhancing the life of a lubricating oil as evidenced by a reduction in viscosity increase, oxidation and nitration, the method comprising:
adding to the lubricating oil additives comprising:
a mixture of neutral and overbased metallic detergents selected from the group consisting essentially of alkaline earth metal sulfonates, phenates, alkylsalicylates, and mixtures thereof in an amount sufficient to provide the composition with a sulfated ash content of from about 0.2 wt % to about 2.0 wt %;
at least 0.1 vol % of a trinuclear molybdenum compound having the formula
Mo3SkLnQz
Where L is an independently selected ligand, n is 1 to 4, k is 4 to 7, Q is a neutral electron donating moiety, and z is 0 to 5;
a dihydrocarbylthiocarbomyl compound;
the amount of trinuclear molybdenum compound and dihydrothiocarbomyl compound being in the range of 0.1 vol % about 2.0 vol %.
10. The method of claim 9 wherein the dihydrothiocarbomyl compound has the formula
Figure US20040110646A1-20040610-C00004
where R1, R2, R3 and R4 are the same or different alkyl groups of from 3 to 30 carbon atoms; X is S, , S—S, SCH2yS, S—CH2CH2(CH3)—S; and y is an integer of 1 to 3.
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Cited By (1)

* Cited by examiner, † Cited by third party
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US20070117724A1 (en) * 2005-11-18 2007-05-24 Cartwright Stanley J Enhanced deposit control for lubricating oils used under sustained high load conditions employing glycerine derivative with a grafted hindered phenolic and/or a hindered phenolic containing a thioether group

Citations (4)

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US4501678A (en) * 1982-06-09 1985-02-26 Idemitsu Kosan Company Limited Lubricants for improving fatigue life
US5719107A (en) * 1996-08-09 1998-02-17 Exxon Chemical Patents Inc Crankcase lubricant for heavy duty diesel oil
US6232276B1 (en) * 1996-12-13 2001-05-15 Infineum Usa L.P. Trinuclear molybdenum multifunctional additive for lubricating oils
US6423670B2 (en) * 2000-03-20 2002-07-23 Infineum International Ltd. Lubricating oil compositions

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4501678A (en) * 1982-06-09 1985-02-26 Idemitsu Kosan Company Limited Lubricants for improving fatigue life
US5719107A (en) * 1996-08-09 1998-02-17 Exxon Chemical Patents Inc Crankcase lubricant for heavy duty diesel oil
US6232276B1 (en) * 1996-12-13 2001-05-15 Infineum Usa L.P. Trinuclear molybdenum multifunctional additive for lubricating oils
US6423670B2 (en) * 2000-03-20 2002-07-23 Infineum International Ltd. Lubricating oil compositions

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20070117724A1 (en) * 2005-11-18 2007-05-24 Cartwright Stanley J Enhanced deposit control for lubricating oils used under sustained high load conditions employing glycerine derivative with a grafted hindered phenolic and/or a hindered phenolic containing a thioether group
US8680030B2 (en) * 2005-11-18 2014-03-25 Exxonmobil Research And Engineering Company Enhanced deposit control for lubricating oils used under sustained high load conditions employing glycerine derivative with a grafted hindered phenolic and/or a hindered phenolic containing a thioether group

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