Classifications

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  • 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
  • C10M163/00—Lubricating 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
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  • C10M167/00—Lubricating compositions characterised by the additive being a mixture of a macromolecular compound, a non-macromolecular compound and a compound of unknown or incompletely defined constitution, each of these compounds being essential
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  • 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
  • C10M2205/022—Ethene
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  • 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
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  • C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
  • C10M2207/10—Carboxylix acids; Neutral salts thereof
  • C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
  • C10M2207/129—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more carbon atoms
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  • 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
  • C10M2207/26—Overbased carboxylic acid salts
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  • 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
  • C10M2207/26—Overbased carboxylic acid salts
  • C10M2207/262—Overbased carboxylic acid salts derived from hydroxy substituted aromatic acids, e.g. salicylates
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  • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
  • C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
  • C10M2209/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
  • C10M2209/08—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate type
  • C10M2209/084—Acrylate; Methacrylate
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  • 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
  • C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
  • C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
  • C10M2215/064—Di- and triaryl amines
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  • C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
  • C10M2215/086—Imides
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  • C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
  • C10M2215/28—Amides; Imides
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  • 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
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  • 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
  • C10M2219/08—Thiols; Sulfides; Polysulfides; Mercaptals
  • C10M2219/082—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
  • C10M2219/087—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Derivatives thereof, e.g. sulfurised phenols
  • C10M2219/089—Overbased salts
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  • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
  • C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
  • C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
  • C10M2223/04—Phosphate esters
  • C10M2223/045—Metal containing thio derivatives
• • C—CHEMISTRY; METALLURGY
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  • 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
  • C10M2227/061—Esters derived from boron
• • C—CHEMISTRY; METALLURGY
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  • 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
  • C10M2227/09—Complexes with metals
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  • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
  • C10M2229/00—Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
  • C10M2229/02—Unspecified siloxanes; Silicones
• • 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
  • C10N2030/04—Detergent property or dispersant property
• • 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
  • C10N2030/40—Low content or no content compositions
  • C10N2030/42—Phosphor free or low phosphor content compositions
• • 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
  • C10N2030/40—Low content or no content compositions
  • C10N2030/43—Sulfur free or low sulfur content compositions
• • 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
  • C10N2030/40—Low content or no content compositions
  • C10N2030/45—Ash-less or low ash content
• • 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
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  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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  • C10N2040/00—Specified use or application for which the lubricating composition is intended
  • C10N2040/25—Internal-combustion engines
  • C10N2040/252—Diesel engines
• • C—CHEMISTRY; METALLURGY
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  • C10N2040/00—Specified use or application for which the lubricating composition is intended
  • C10N2040/25—Internal-combustion engines
  • C10N2040/252—Diesel engines
  • C10N2040/253—Small diesel engines
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  • 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 present invention relates to lubricating oil compositions. More specifically, the present invention relates to lubricating oil compositions that have reduced levels of sulfated ash, phosphorus and sulfur (low “SAPS”), yet provide improved lubricant performance in internal combustion engines.
• SAPS sulfated ash, phosphorus and sulfur
• Catalytic converters typically contain one or more oxidation catalysts, NO x storage catalysts, and/or NH 3 reduction catalysts.
• the catalysts contained therein generally comprise a combination of catalytic metals such as platinum, and metal oxides.
• Catalytic converters are installed in the exhaust systems, for example, the exhaust pipes of automobiles, to convert the toxic gases to nontoxic gases.
• the use of catalytic converters is thought to be essential in bucking global warming trends and combating other environmental detriments.
• the catalysts however, can be poisoned and rendered less effective, if not useless, as a result of exposure to certain elements or compounds, especially phosphorus compounds.
• phosphorus compounds may be introduced into the exhaust gas is the degradation of phosphorus-containing lubricating oil additives.
• Examples of phosphorus lubricating oil additives include zinc dialkyldithiophosphates and the like.
• Zinc dialkyldithiophosphates are among the most effective and conventionally used antioxidants and antiwear agents, from both a performance and cost-effectiveness standpoint, in lubricating oil compositions. While they are effective antioxidants and antiwear agents, the phosphorus, sulfur and ash they introduce into the engine react with the catalysts and may shorten the service life, of the catalytic converters.
• Reduction catalysts are susceptible to damage by sulfur and sulfur compounds in the exhaust gas, which are introduced by the degradations of both the base oil used to blend the lubricants and sulfur-containing lubricant oil additives.
• sulfur-containing lubricant oil additives include, but are not limited to, magnesium sulfonate and other sulfated or sulfonated detergents.
• Particulate traps are usually installed in the exhaust system, especially in diesel engines, to prevent the carbon black particles or very fine condensate particles or agglomerates thereof (i.e., “diesel soot”) from being released into the environment. Aside from polluting air, water, and other elements of the environment, diesel soot is a recognized carcinogen. These traps, however, can be blocked by metallic ash which is the degradation product of metal-containing, lubricating oil additives including common ash-producing detergent additives.
• lubricating oil additives that exert a minimum negative impact on such devices.
• OEMs often set various limits for maximum sulfur, phosphorus, and/or sulfated ash levels for “new service fill” and “first fill” lubricants. For instance, when used in light-duty passenger-car internal combustion engines, the sulfur levels are typically required to be at or below 0,30 wt. %, the phosphorus levels at or below 0.08 wt. %, and the sulfated ash contents at or below 0.8 wt. %.
• the maximum sulfur, phosphorus and/or sulfated ash levels may differ, however, when the lubricating compositions are used in heavy-duty internal combustion engines.
• the maximum sulfated ash level may be as high as 1.0 wt. % in those heavy-duty engines.
• Such lubricating oil compositions are also referred to as “low SAPS” (low sulfated ash, phosphorus, sulfur) lubricating oil compositions for gasoline engines, and “LEDL” (low emission diesel lubricant) oil compositions for diesel engines.
• low SAPS low sulfated ash, phosphorus, sulfur
• LEDL low emission diesel lubricant
• a lubricant meeting the ACEA gasoline and diesel engine low SAPS specification must pass, inter alia, the “CEC L-78-T-99” test, which measures the cleanliness and extent of piston ring sticking after running a Volkswagen turbocharged direct injection automotive diesel engine for art extended time period, cycling alternatively between idle and full power. Similar specifications and testing standards of varied stringencies can also be found in other countries and regions, such as Japan, Canada, and the United States.
• a companion application, U.S. patent application Ser. No. 11/218,647 (published as U.S. 2006/005820) disclosed a low SAPS lubricating oil composition with similar advantages. That composition comprised (a) a major amount of an oil of lubricating viscosity; (b) at least one nitrogen-containing dispersant to provide a nitrogen content of at least 0.075 wt. %, the dispersant having a polyalkenyl backbone of molecular weight of about 900 to about 3000 Daltons; and (c) an oil-soluble or oil-dispersible source of boron to provide a wt.
• Low SAPS lubricating oil compositions have also been known to impart certain other desirable properties.
• an internal combustion engine oil of this kind was reported to retain high total base number (TBN) in U.S. patent application Ser. No. 11/176,424 (published as U.S. 2006/0014653).
• the composition had a sulfated ash content of not greater than 0.9 wt. %, and a phosphorus content from 0.04 to 0.1 wt. %.
• the composition contained base oil; one or more detergents selected from phenste detergents, salicylate detergents, and sulphonate detergents, wherein said one or more detergents each, independently, had a TEN value of from 30 to 350 mg KOH/g; and at least 3.5 wt. % of one or more antioxidants selected from the group of aminic antioxidants and phenolic antioxidants.
• U.S. patent application Ser. No. 11/288,600 (published as U.S. 2006/0116300) disclosed a low SAPS lubricating oil composition that provided improved lubricant performance, and especially antiwear properties, in compression-ignited diesel engines according to a Mack T10 screener test.
• That low SAPS lubricating oil composition comprised (1) a major amount of an oil of lubricating viscosity; (2) a minor amount of a calcium salicylate detergent; (3) a minor amount of an overbased magnesium detergent; and (4) a minor amount of a basic, low molecular weight nitrogen-containing dispersant derived from a polymer having a number average molecular weight of no greater than 1100 Daltons.
• reaction products of polyisobutylenes and mono unsaturated acylating agents when accompanied by at least one ashless dispersant, at least one metal-containing detergent, at least one antiwear additive, and at least one antioxidant, significantly enhance piston cleanliness control in internal combustion engines.
• the present invention therefore provides a low sulfated ash, low phosphorus and low sulfer lubricant composition, including an additive package or a concentrate, comprising such a reaction product of a polyisobutylene and a monounsaturated acylating agent.
• the present invention also provides methods of using and making such a lubricating oil composition.
• a reaction product of a polyisobutylene and a monounsaturated acylating agent is typically prepared from its non-carboxylated poly isobutylene precursor.
• Polyisobutylenes are also known as polyisobutenes to persons skilled in the art. They have also been given the name “butyl rubber,” as they are much used in that capacity. In the lubricant and/or fuel additive field, PIBs have found wide use as dispersants, viscosity improvers, thickeners, and the like.
• PIBs have been summarized, far example, in section 3.3 (page 846) of Speight, C HEMISTRY & T ECHNOLOGY of P ETROLEUM C HEMICAL I NDUSTRIES, v. 76. 3d ed. (N.Y. Marcel Dekker. Inc., 1999); and in section 4.1 of Immel, U LMANN'S E NCYCLOPEDIA of I NDUSTRIAL C HEMISTRY (Wiley-VCH Verlag GmbH & Go, KGaA, 2002).
• Useful PIBs generally contain residual unsaturation in amounts of about one ethylene double bond per polymer chain, positioned anywhere along the chain.
• the PIBs are prepared from a pure isobutylene steam or a Raffinate I stream, resulting in a reactive isobutylene polymer with terminal vinylidene olefins.
• HR-PIBs highly reactive polyisobutylenes
• a useful HR-PIBs would have a terminal vinylidene content of at least about 50%, for example, at least about 55%, or at least about 65%, or at least about 70%, or at least about 80%, or more preferably, at least about 85%,
• Such HR-PIBs can Be prepared according to various art-recognized techniques, such as, for example, those described in U.S. Pat. Nos. 4,152,499 and 4,605,808. Relevant disclosures of these patents, to the extent they do not conflict with the disclosures and claims herein, are incorporated by reference.
• Certain HR-PIBs are commercially available, for example, under the trade name of GLISSOPALTM (from BASF®).
• Reaction products of PIBs and monounsaturated acylating agents have been used as precursors in manufacturing ashless dispersants.
• succinic anhydride derivatives namely, the polyisobutylene succcinic anhydrides (PIBSAs)
• PIBSAs polyisobutylene succcinic anhydrides
• Examples of such use can be found in U.S. Pat. Nos. 5,827,806 and 6,245,725, each disclosing, inter alia, the making of a preferred set of nitrogen-containing ashless dispersants from certain PIBSAs, polyethylene amines (e.g., tetraethylene pentamine, polyoxypropylene diamine), and aminoalcohols (e.g., triemethylolaminomethane).
• polyethylene amines e.g., tetraethylene pentamine, polyoxypropylene diamine
• aminoalcohols e.g., triemethylolaminomethane
• PIBSAs have also been applied directly, i.e., without derivatization, as dispersants.
• U.S. Pat. No. 6,632,781 disclosed using a dispersant mixture comprising a polyalkylene succinic dispersant selected from the group consisting of; (1) a polyalkylene succinic anhydride, preferably a PIBSA; (2) a non-nitrogen containing derivative of the polyalkylene succinic anhydride; and (3) mixtures of polyalkylene succinic anhydrides; (4) mixtures of non-nitrogen containing derivatives of the polyalkylene succinic anhydride; and (5) mixtures of one or more polyalkylene succinic anhydrides and one or more non-nitrogen containing derivatives of polyalkylene succinic anhydrides. That dispersant was said to impart enhanced water tolerance and lubricant-oil compatibility for alkali metal borates.
• the present invention provides a low sulfated ash, low phosphorus and low sulfur lubricant composition, including an additive package or a concentrate, comprising at least one reaction product of a PIB and a monounsaturated acylating agent.
• the lubricant additive compositions of the invention provide superior piston cleanliness, but are also compatible for low SAPS applications.
• the present invention further provides methods of applying and making these compositions.
• the present invention provides lubricating oil compositions that provide high piston cleanliness, especially when the machines housing those compositions operate at elevated temperatures, but which introduce low levels of phosphorous, low levels of sulfur, and low levels of sulfated ash to the internal combustion engines.
• the levels of phosphorous in the lubricating oil compositions of the present invention are typically at or below about 0.09 wt. %, and preferably at or be low about 0.08 wt. %, and more preferably at or below about 0.07 wt. %. and particularly preferably at or below about 0.05 wt. %.
• the levels of sulfur produced by the lubricating oil compositions of the present invention are typically at m below about 0.30 wt.
• the levels of sulfated ash produced by the lubricating oil compositions of the present invention are typically at or below about 1.60 wt. %, but preferably at or below about 1.00 wt. %, more preferably at or below about 0.80 wt. %, even more preferably at or below about 0.50 wt. %, and particularly preferably at or below about 0.45 wt. %.
• the level of sulfated ash will be from above about 0,50 to about 1.60 wt. %, preferably from above about 0.5 to about 0.8 wt. %.
• the present lubricating compositions are more desirable from an environmental standpoint than the conventional internal combustion engine lubricating oils that contain higher phosphorous, sulfur and sulfated ash.
• the compositions of the present invention facilitate longer service lives for the catalytic converters and the particulate traps, while providing the desired piston cleanliness.
• the present lubricating oil composition comprises;
• a piston-cleanliness-enhancing amount of at least one reaction product of a polyisobutylene and a monounsaturated acylating agent wherein the polyisobutylene has a number average molecular weight of about 200 to about 5000 Daltons, preferably from about 500 to about 4500 Daltons: wherein, based on the total weight of the lubricating composition, the phosphorus content is no more than about 0.09 wt. %; the sulfur content is no more than about 0.3 wt. %; and the sulfated ash content is no more than about 1.6 wt. %.
• the reaction product of a polyisobutylene and a monounsaturated acylating agent may be one represented by either Formula A or Formula B:
• R 1 is a polyisobutylene chain of number average molecular weight of about 200 to about 5000 Daltons, preferably from about 500 to about 4500 Daltons; and R 2 is a carboxyl-containing group.
• the lubricating oil composition of this aspect may optionally further comprise one or more additives selected from; (1) antiwear agents; (2) friction modifiers; (3) antioxidants; (4) corrosion inhibitors; (5) anti-foam additives; (6) seat fixes or seal pacifiers; (7) pour point depressants; (8) viscosity index modifiers; and (9) multifunctional additives.
• additives selected from; (1) antiwear agents; (2) friction modifiers; (3) antioxidants; (4) corrosion inhibitors; (5) anti-foam additives; (6) seat fixes or seal pacifiers; (7) pour point depressants; (8) viscosity index modifiers; and (9) multifunctional additives.
• the invention provides an additive package composition or a concentrate comprising at least one reaction product of a PIB and a monounsaturated acylating agent in an organic diluent liquid, for example, base oil.
• the additive package composition or concentrate of this aspect preferably further comprises various other additives desired in lubricating oil, such as, for example, ashless dispersants, metal-containing detergents, antiwear additives, antioxidants, friction modifiers, corrosion inhibitors, anti-foam additives, pour point depressants, viscosity index improvers, and seal fixes or seal pacifiers.
• the invention provides a method of operating an internal combustion engine provided with one or more exhaust gas after-treatment devices, which method comprises lubricating said engine with a lubricating composition of the first aspect, or with an additive package composition or a concentrate of the second aspect.
• the invention provides a method of preparing a lubricating oil composition of the first aspect or an additive package or a concentrate of the second aspect.
• the present invention provides lubricating oil compositions as described above.
• the compositions have a total sulfur content of at or below about 0.30 wt. % in typical embodiments, at or below about 0.20 wt. % in some other embodiments, and at or below about 0.10 wt. % in further embodiments.
• the major source of sulfur in the composition of the invention is often the base stocks and the additives.
• An exemplary lubricating oil composition of the present invention contains about 0.2 wt. % of sulfur, based on the total weight of the composition.
• the lubricating oil compositions have a total phosphorus content of at or below about 0.09 wt. % in typical embodiments, at or below about 0,08 wt. % in some other embodiments, at or below about 0.07 wt. % in yet other embodiments, and at or below about 0.05 wt. % in further embodiments.
• An exemplary lubricating oil composition of the present invention contains about 0.07 wt. % of phosphorus, based on the total weight of the composition.
• the lubricating oil compositions have a total sulfated ash content of, as determined by the ASTM D-874, at or below about 1.60 wt. % in typical embodiments, at or below about 1.00 wt. % in some other embodiments, at or below about 0.80 wt. % in yet other embodiments, at or below about 0.50 wt. % in some other embodiments, and at or below about 0.45 wt. % in further embodiments.
• An exemplary lubricating oil composition of the present invention has a sulfated ash content of about 0.6 wt. %, based on the weight of the lubricant compositions.
• Another exemplary lubricating oil composition of the present invention has a sulfated ash content of about 0.8 wt. %, based on the weight of the lubricant composition.
• the low-SAPS lubricating oil composition of the present invention is comprised of one or more base oils, which are present in a major amount (i.e., an amount greater than about 50 wt. %).
• the base oil is present in an amount greater than about 60 wt. %, or greater than about 70 wt. %, or greater than about 80 wt. % of the lubricating oil composition.
• the base oil sulfur content is typically less than about 1.00 wt. %, preferably less than about 0.60 wt. %, more preferably less than about 0.40 wt. %, and particularly preferably less than about 0.30 wt. %,
• the low-SAPS lubricating oil composition may have a viscosity at 100° C. of up to about 16.3 mm 2 /s, and in one embodiment of about 5 to about 16.3 mm 2 /s (cSt), and in one embodiment of about 6 to about 13 mm 2 /s (cSt).
• the low-SAPS lubricating oil composition may have a high-temperature/high-shear viscosity at 150° C.
• the base oil used in the lubricant compositions of the invention may be a natural oil, a synthetic oil, or a mixture thereof provided that the sulfur content of such an oil does not exceed the above-indicated sulfur concentration limit required to sustain the low SAPS lubricating oil compositions.
• the natural oils that are suitable include animal oils and vegetable oils (e.g., castor oil, lard oil).
• the natural oils may also include 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. Oils derived from coal or shale are also useful.
• Synthetic lubricating oils include hydrocarbon oils such as polymerized and interpolymerized olefins (e.g., polybutylenes, polypropylenes, propylene isobutylene copolymers, etc.); poly(1-hexenes), poly-(1-octenes), poly(1-decenes), etc. and mixtures thereof; alkylbenzenes (e.g., dodecylbenzenes, tetradecylbenzenes, dinonylbenzenes, di-(2-ethylhexyl)benzenes, etc.); polyphenyls (e.g., biphenyls.
• hydrocarbon oils such as polymerized and interpolymerized olefins (e.g., polybutylenes, polypropylenes, propylene isobutylene copolymers, etc.); poly(1-hexenes), poly-(1-octenes), poly
• Synthetic lubricating oils also include oils prepared by a known Fischer-Tropsch gas-to-liquid synthetic procedure.
• Another class of known synthetic lubricating oils includes alkylene oxide polymers and interpolymers and derivatives thereof where the terminal hydroxyl groups have been modified by a process such as esterification or etherification.
• these synthetic oils include polyoxyalkylene polymers prepared by polymerization of ethylene oxide or propylene oxide, and the alkyl and aryl ethers of polyoxyalkylene polymers (e.g., methyl-polyiso-propylene glycol ether having a molecular weight of 1000 Daltons or diphenyl ether of poly-ethylene glycol having a molecular weight of 1000 to 1500 Daltons); and mono- and polycarboxylic esters thereof (e.g., acetic acid esters, mixed C 3 -C 8 fatty acid esters, and C 13 Oxo acid diester of tetraethylene glycol).
• esters of dicarboxylic acids e.g., phthalic acid, succinic acid, alkyl succinic acids and alkenyl succinic acids, maleic acid, azelaic acid, suberic acid, sebasic acid, fumaric acid, adipic acid, linoleic acid dimer, malonic acid, alkylmalonic acids, alkenyl malonic acids
• alcohols e.g., butyl alcohol, hexyl alcohol, dodecyl alcohol, 2-ethylhexyl alcohol, ethylene glycol, diethylene glycol monoether, propylene glycol.
• esters includes dibutyl adipate, di(2-ethylhexyl) sebacate, di-n-hexyl fumarate, dioctyl sebacate, diisooctyl azelate, diisodecyl azelate, dioctyl phthalate, didecyl phthalate, dieicosyl sebacate, the 2-ethylhexyl diester of linoleic acid dimer, and the complex ester formed by reacting one mole of sebacic acid with two moles of tetraethylene glycol and two moles of 2-ethylhexanoic acid and the like.
• Esters useful as synthetic oils also include those made from C 5 to C 12 monocarboxylic acids and polyols and polyol esters such as neopentyl glycol, trimethylolpropane, pentaerythritol, dipentaerythritol and tripentaerythritol.
• the synthetic oil can also be a poly-alpha-olefin (PAO).
• PAOs are derived from monomers having from 4 to 30, or from 4 to 20, or from 6 to 16 carbon atoms.
• Examples of useful PAOs include those derived from octene, decene, mixtures thereof, and the like. These PAOs may have a viscosity from about 2 to about 15, or from about 3 to about 12, or from about 4 to about 8 mm 2 /s (cSt) at 100° C. Mixtures of mineral oil with one or more of the foregoing PAOs may be used.
• Unrefined, refined and rerefined oils either natural or synthetic (as well as mixtures, of two or more) of the types of oils disclosed above can be used in the lubricating compositions of the present invention.
• Unrefined (or raw) oils are those obtained directly from a natural or synthetic source without further purification treatment.
• Refined oils are similar-to the unrefined oils except they have been further treated in one or more purification steps. Many such purification techniques are known to those skilled in the art such as solvent extraction, secondary distillation, acid or base extraction, filtration, percolation, and the like.
• Rerefined oils are oils that have been used in service but are subsequently treated so that they may be re-applied, in service. Because the used oils almost always contain spent additives and breakdown products, in addition to the standard oil refining steps, steps that would remove the spent additives and breakdown products must be taken.
• Such rerefined oils are also known as reclaimed or reprocessed oils.
• reaction products of polyisobutylenes and monounsaturated acylating agents may be represented by either Formula A or Formula B, as listed below:
• R 1 is a polyisobutylene (PIB) chain; and R 2 is a carboxyl-containing group.
• PIB polyisobutylene
• the R 1 of Formula A and/or Formula B is a PIB chain.
• Suitable PIBs that many constitute the chain may be any PIBs that have a number average weight of about 200 to about 5000 Daltons, preferably from about 500 to about 4500 Daltons, particularly preferably from about 1000 to about 3500 Daltons.
• An exemplary lubricating oil composition of the present invention incorporates a PIB that has a number average molecular weight of about 2300 Daltons.
• the R 2 of Formula A and/or Formula B is a carboxyl-containing group derived from a monocarboxylic acid, dicarboxylic acid, dicaxboxylic acid anhydride, anhydride-producing material, or derivatives thereof.
• Such materials may include, for example, acids, anhydrides, or acid esters.
• such materials may include one or more selected from: (1) monounsaturated C 4 to C 20 dicarboxylic acids, wherein (a) the carboxyl groups are vicinyl (i.e., located on adjacent carbon atoms), and (b) at least one, preferably both, of said adjacent carbon atoms are part of said mono-unsaturation; (2) derivatives of (1) such as anhydrides and/or C 1 to C 10 alcohol-derived monoesters or diesters of (1); (3) monounsaturated C 3 to C 20 monocarboxylic acids wherein each of the carbon-carbon double bonds is conjugated with the carboxyl group, i.e., is of the structure: —C ⁇ C—CO—; and (4) derivatives of (3) such as C 1 to C 10 alcohol-derived monoesters or diesters of (3).
• monounsaturated C 4 to C 20 dicarboxylic acids wherein (a) the carboxyl groups are vicinyl (i.e., located on adjacent carbon atoms), and (b
• the R 2 of Formula A and/or Formula B can also be derived from a mixture comprising any proportions of 2 or more of materials (1) to (4).
• materials are also termed “monounsaturated acylating agents” herein.
• the monounsaturation of each of the monocarboxylic acids, dicarboxylic acids, anhydrides, or derivatives thereof becomes saturated.
• maleic anhydride becomes backbone substituted succinic anhydride
• acrylic acid becomes back-bone substituted propionic acid.
• Exemplary monounsaturated carboxylic reactants include fumaric acid, itaconic acid, maleic acid, maleic anhydride, chloromaleic acid, chloromaleic anhydride, acrylic acid, methacrylic acid, crotonic acid, cinnamic acid, and lower and intermediate alkyl (e.g., C 1 to C 10 alkyl) acid esters of the foregoing.
• suitable alkyl acid esters include methyl maleate, ethyl fumarate, methyl fumarate, and the like.
• a particularly preferred monocarboxylic acid-, dicarboxylic acid-, or anhydride-producing material is maleic anhydride.
• a preferred reaction product of a PIB and a monounsaturated acylating agent is a polyisobutylene succinic anhydride (PIBSA).
• the reaction product of a PIB and a monounsaturated acylating agent of the present invention can be prepared by known procedures.
• an HR-FIB precursor of Formula A and/or Formula B can be prepared by a cationic polymerization process, at a temperature that is predetermined according to the desired molecular weight for the PIB oligomer.
• a PIB that has an average molecular weight of about 2300 Daltons can be prepared at a temperature of about 5° F.
• a catalyst such as BF 3 is often used to advance the polymerization. Following the reaction, the catalyst is typically removed, for example, by extracting the catalyst dissolved in a hot distilled water phase.
• the feed into the reactor may include materials such as hexanes and isopropanol.
• the unreacted residuals of reactive materials, including the unreacted isobutylene monomers, are often removed or purified from the PIB oligomers according to known methods, such as, for example, by flashing in a flash drum and/or using an extraction column.
• Some HR-PIBs are also commercially available, for example, under the trade name of GLISSOPALTM (by BASF®).
• Reaction products of such HE-PIBs and monounsaturated acylating agents can be prepared according to known methods.
• the succinic anhydride derivative of PIB i.e., PIBSA
• PIBSA succinic anhydride derivative of PIB
• a PIBSA can be prepared using a catalyzed “thermal” or “ene” process, wherein the polyisobutylene is reacted with maleic anhydride at an elevated temperature in the presence of sulfonic acid or one or more other strong-acid.
• This process is capable of producing PIBSAs with a range of apparent succinic ratios. Such ratios may be adjusted to attain the desired apparent succinic ratios by modifying reaction parameters such as, for example, the length of time it takes to inject the sulfonic acid or one or more strong acids into the reactor, the maleic anhydride:PIB charge mole ratio, and the reaction hold time.
• the apparent succinic ratio is preferably in the range of between about 1 and about 2, preferably between about 1.2 to about 1.6, more preferably between about 1.3 and about 1.4.
• Various PIBSA products can also be obtained from commercial vendors such as Chevron Oronite Company LLC.
• the reaction products of PIBs and monounsaturated acylating agents may be present in the lubricating oil compositions of the present invention in an amount that is sufficient to provide substantially enhanced piston-cleanliness and/or maintain such cleanliness in internal combustion engines.
• substantially enhanced it is meant that the pistons are measurably cleaner when assessed against standards of various countries and regions, such as the ACEA standards in Europe and the JASO standards in Japan.
• the amount of one or more reaction products of PIBs and monounsaturated acylating agents is about 0.01 to about 5.00 wt. %, more preferably, about 0.50 to about 4.00 wt. %, particularly preferably, about 1.00 wt.
• An exemplary lubricating oil composition of the present invention comprised about 2.00 wt. % of a PIBSA, wherein the PIB chain has a number average molecular weight of about 2300 Daltons.
• Metal-containing or ash-forming detergents function both as detergents to reduce or remove deposits and as acid neutralizers or rust inhibitors, thereby reducing wear and corrosion and extending engine life.
• Detergents generally comprise a polar head with long hydrophobic tail, with the polar head comprising a metal salt of an acid organic compound.
• the composition of the present invention may contain one or more detergents, which are normally salts, and especially overbased salts. Overbased salts, or overbased materials, are single phase, homogeneous Newtonian systems characterized by a metal content in excess of that which would be present according to the stoichiometry of the metal and the particular acidic organic compound reacted with the metal.
• the overbased materials are prepared by reacting an acidic material (typically an inorganic acid or lower carboxylic acid, preferably carbon dioxide) with a mixture comprising an acidic organic compound, in a reaction medium comprising at least one inert, organic solvent (such as mineral oil, naphtha, toluene, xylene) in the presence of a stoichiometric excess of a metal base and a promoter,
• an acidic material typically an inorganic acid or lower carboxylic acid, preferably carbon dioxide
• a mixture comprising an acidic organic compound
• a reaction medium comprising at least one inert, organic solvent (such as mineral oil, naphtha, toluene, xylene) in the presence of a stoichiometric excess of a metal base and a promoter
• the acidic organic compounds useful in making the overbased compositions of the present invention include carboxylic acids, sulfonic acids, phosphorus-containing acids, phenols or mixtures thereof.
• the acidic organic compounds are carboxylic acids or sulfonic acids with sulfonic or thiosulfonic groups (such as hydrocarbyl-substituted benzenesulfonic acids), and hydrocarbyl-substituted salicylic acids.
• Carboxylate detergents e.g., salicylates
• an aromatic carboxylic acid can be prepared by reacting an aromatic carboxylic acid with an appropriate metal compound such as an oxide or hydroxide. Neutral or overbased products may then be obtained by methods well known in the art.
• the aromatic moiety of the aromatic carboxylic acid can contain heteroatoms, such as nitrogen and oxygen. Preferably, the moiety contains only carbon atoms. More preferably, the moiety contains six or more carbon atoms, such as a benzene moiety.
• the aromatic carboxylic acid may contain one or more aromatic moieties, such as one or more benzene rings, fused or otherwise connected via alkylene bridges.
• aromatic carboxylic acids examples include salicylic acids and sulfurized derivatives thereof, such as hydrocarbyl substituted salicylic acid and derivatives thereof.
• Processes for sulfurizing, for example a hydrocarbyl-subtituted salicylic acid are known to those skilled in the art.
• Salicylic acids are typically prepared by carboxylation, for example, by the Kolbe-Schmitt process, of phenoxides. In that case, salicylic acids are generally obtained in a diluent in admixture with uncarboxylated phenol.
• Sulfonates can be prepared by using sulfonic acid in to sulfoniate alkyl-substituted aromatic hydrocarbons such as those obtained from the fractionation of petroleum or those obtained from alkylation of aromatic hydrocarbons.
• Alkaryl sulfonates usually contain from about 9 to about 80 or more carbon atoms, preferably from about 16 to about 60 carbon atoms per alkyl substituted aromatic moiety.
• Metal salts of phenols and sulfurized phenols are prepared by reaction with an appropriate metal compound such as an oxide or hydroxide. Neutral or overbased products may be obtained by methods well known in the art.
• sulfurized phenols may be prepared by reacting a phenol with sulfur or a sulfur-containing compound such as hydrogen sulfide, sulfur monohalide or sulfur dihalide, to form products that are mixtures of compounds in which 2 or more phenols are bridged by sulfur-containing bridges.
• the metal compounds useful in making the overbased salts are generally any Group 1 or Group 2 metal compounds in the Periodic Table of the Elements.
• the Group 1 metals of the metal compound include Group 1a alkali metals (e.g., sodium, potassium, lithium) as well as Group 1b metals such as copper.
• the Group 1 metals are preferably sodium, potassium, lithium and copper, more preferably sodium or potassium, and particularly preferably sodium.
• the Group 2 metals of the metal base include the Group 2a alkaline earth metals (e.g., magnesium, calcium, strontium, barium) as well as the Group 2b metals such as zinc or cadmium.
• the Group 2 metals are magnesium, calcium, barium, or zinc, more preferably magnesium or calcium, particularly preferably calcium.
• overbased detergents examples include, but are not limited to calcium sulfonates, calcium phenates, calcium salicylates, calcium stearates and mixtures thereof.
• Overbased detergents suitable for use with the lubricating oils of the present invention may be low overbased (i.e., Total Base Number (TBN) below about 100).
• TBN of such a low-overbased detergent may be from about 5 to about 50, or from about 10 to about 30, or from about 15 to about 20.
• the overbased detergents suitable for use with the lubricating oils of the present invention may alternatively be high overbased (i.e., TBN above about 100).
• the TBN of such a high-overbased detergent may be from about 150 to about 450, or from about 200 to about 350, or from about 250 to about 280.
• a low-overbased calcium sulfonate detergent with a TEN of about 17, and a high-overbased calcium sulfurized phenate with a TBN of about 260 are two exemplary overbased detergents in the lubricating oil compositions of the present invention.
• the lubricating oil compositions of the present invention may comprise more than one overbased detergents, which may be all low-TBN detergents, all high-TBN detergents, or a mix of the those two types.
• the amount of the overbased detergent(s), if present, may be about 0.05 to about 16 mM, or about 3 to about 15 mM, or about 4 to about 14 mM. In an exemplary embodiment of the present invention, about 4 mM of a low-TBN detergent plus about 10 mM of a high-TBN detergent are present in the lubricating oil composition.
• Suitable detergents for the lubricating oil compositions of the present invention also include “hybrid” detergents such as, for example, phenate/salicylates, sulfonate/phenates, sulfonate/salicylates, sulfonates/phenates/salicylates, and the like.
• Hybrid detergents have been described, for example, in U.S. Pat. Nos. 6,153,565, 6,281,179, 6,429,178, and 6.429,179. Relevant disclosures of these patent applications and patents, to the extent they do not conflict with the disclosures and claims herein, are incorporated by reference.
• Dispersants are generally used to maintain in suspension insoluble materials resulting, from oxidation during use, thus preventing sludge flocculation arid precipitation or deposition on metal parts.
• Nitrogen-containing ashless (metal-free) dispersants are basic, and contribute to the TBN of a lubricating oil composition to which they are added, without introducing additional sulfated ash.
• An ashless dispersant generally comprises an oil soluble polymeric hydrocarbon backbone having functional groups that are capable of associating with particles to be dispersed. Many types of ashless dispersants are known in the art.
• Typical dispersants include, but are not limited to, amines, alcohols, amides, or ester polar moieties attached to the polymer backbones via bridging groups.
• the ashless dispersant of the present invention may be, for example, selected from oil soluble sails, esters, ammo-esters, amides, imides, and oxazolines of long chain hydrocarbon substituted mono and dicarboxylic acids or their anhydrides; thiocarboxylate derivatives of long chain hydrocarbons, long chain aliphatic hydrocarbons having a polyamine attached directly thereto; and Mannich condensation products formed by condensing a long chain substituted phenol with, formaldehyde and polyalkylene polyamine.
• Carboxylic dispersants are reaction products of carboxylic acylating agents (acids, anhydrides, esters, etc;) comprising at least 34 and preferably at least 54 carbon atoms with nitrogen containing compounds (such as amines), organic hydroxy compounds (such as aliphatic compounds including monohydric and polyhydric alcohols, or aromatic compounds including phenols and naphthols), and/or basic inorganic materials. These reaction products include imides, amides, and esters.
• Succinimide dispersants are a type of carboxylic dispersants. They are produced by reacting hydrocarbyl-substituted succinic acylating agent with organic hydroxy compounds, or with amines comprising at least one hydrogen atom attached to a nitrogen atom, or with a mixture of the hydroxy compounds and amines.
• succinic acylating agent refers to a hydrocarbon-substituted succinic acid or a succinic acid-producing compound, the latter encompasses the acid itself.
• Such materials typically include hydrocarbyl-substituted succinic acids, anhydrides, esters (including half esters) and halides.
• Succinic-based dispersants have a wide variety of chemical structures, which may be represented by the formula:
• each R 1 is independently a hydrocarbyl group, such as a polyolefin-derived group.
• the hydrocarbyl group is an alkyl group, such as a polyisobutyl group.
• the R 1 groups can contain about 40 to about 500 carbon atoms, and these atoms may be present in aliphatic forms.
• R 2 is an alkylene group, commonly an ethylene (C 2 H 4 ) group.
• Succinimide dispersants have been more folly described in, for example, U.S. Pat. Nos. 4,234,435, 3,172,892 and 6,165,235. Relevant disclosures of these patents, to the extend they do not conflict with the disclosures herein, are incorporated by reference.
• the polyalkenes from which the substituent groups are derived are typically homopolymers and interpolymers of polymerizable olefin monomers of 2 to 16 carbon atoms, and usually 2 to 6 carbon atoms.
• the amines which are reacted with the succinic acylating agents to form the carboxylic dispersant composition can be monoamines or polyamines.
• Succinimide dispersants are referred to as such since they normally contains nitrogen largely in the form of imide functionality, although the amide functionality may be m the form of amine salts, amides, imidazolines as well as mixtures thereof.
• a succinimide dispersant one or more succinic acid-producing compounds and one or more amines are heated and typically water is removed, optionally in the presence of a normally liquid and substantially inert organic liquid solvent/diluent.
• the reaction temperature is generally in the range of about 80° C. up to the decomposition temperature of the mixture or the product, which typically falls between about 100° C. and about 30° C.
• Suitable ashless dispersants may also include amine dispersants, which are reaction products of relatively high molecular weight aliphatic halides and amines, preferably polyalkylene polyamines. Examples thereof have been described, for example, in U.S. Pat. Nos. 3,275,554, 3,438,757, 3,454,555, 3,565,804, and the like. Relevant disclosures of these patents, to the extend they do not conflict with the disclosures herein, are also incorporated by reference.
• Suitable ashless dispersants may further include “Mannich dispersants,” which are reaction products of alkyl phenols in which the alkyl group contains at least 30 carbon atoms with aldehydes (especially formaldehyde) and amines (especially polyalkylene polyamines). These dispersants have been described, for example, in U.S. Pat. Nos. 3,036,003, 3,586,629, 3,591,598, 3,980,569, and the like. Relevant disclosures of these patents, to the extent they do not conflict with the disclosures and claims herein, are likewise incorporated by reference.
• Suitable ashless dispersants may even include post-treated dispersants, which are obtained by reacting carboxylic, amine or Mannich dispersants with reagents such as dimercaptothiazoles, urea, thiourea, carbon disulfide, aldehydes, ketones, carboxylic acids, hydrocarbon-substituted succinic anhydrides, nitrile epoxides, boron compounds and the like.
• Post-treated dispersants have been described, for example, in U.S. Pat. Nos. 3,329,658, 3,449,250, 3,666,730, aid the like. Relevant disclosures of these patents, to the extent they do not conflict with the disclosures and claims herein, are further incorporated by reference.
• Suitable ashless dispersants may be polymeric, which are interpolymers of oil-solubilizing monomers such as decyl methacrylate, vinyl decyl ether and high molecular weight olefins with monomers containing polar substitutes.
• Polymeric dispersants have been described, for example, in U.S. Pat. Nos. 3,329,658, 3,449,250, 3,666,730, and the like. Relevant disclosures of these patents, to the extent they do not conflict with the disclosures and claims herein, are similarly incorporated by reference,
• a bissuccinimide treated with ethylene carbonate was used as the ashless dispersant.
• the dispersant(s) of the present Invention are preferably non-polymeric (e.g., are mono- or bissuccinimides).
• the ashless dispersant is suitably present in an amount of about 0.5 to about 10.0 wt. %, preferably about 3.0 to about 7.0 wt. %.
• An exemplary lubricating oil composition of the present invention comprises an ethylene-carbonate treated bissuccinimide dispersant derived from a PIBSA wherein the PIB chain has a number average molecular weight of about 2300 Daltons (PIBSA 2300) In an amount of about 6.5 wt. %.
• Another lubricating oil composition of the present invention comprises a similar dispersant in an amount of about 6.0 wt.
• the lubricating oil composition comprises from about 0.01 to about 0.35 wt. %, preferably from about 0.05 to about 0.25 wt. %, particularly preferably from about 0.08 to about 0.1.2 wt. % of total nitrogen from dispersant.
• the lubricating oil compositions of the present invention may optionally comprise various other additives, including, but not limited to, antiwear agents, friction modifiers, antioxidants, corrosion inhibitors, viscosity index improvers, and other additives commonly used to lubricate internal combustion engines.
• Dihydrocarbyl dithiophosphate metal salts are frequently used as antiwear and antioxidant agents.
• the metal may be an alkali or alkaline earth metal, or aluminum, lead, tin, molybdenum, manganese, nickel or copper.
• the zinc salts are the most commonly used in lubricating oil in amounts of about 0.1 to about 10 wt. %, preferably about 0.2 to about 2 wt. %, based upon the total weight of the lubricating oil composition. They may be prepared in accordance with known techniques by first forming a dihydrocarbyl dithiophosphoric acid (DDPA), usually by reaction of one or more alcohol or a phenol with P 2 S 5 and then neutralizing the formed DDPA with a zinc compound.
• DDPA dihydrocarbyl dithiophosphoric acid
• a dithiophosphoric acid may be made by reacting mixtures of primary and secondary alcohols.
• multiple dithiophosphoric acids can he prepared where the hydrocarbyl groups on one are entirely secondary in character and the hydrocarbyl groups on the others are entirely primary in character.
• any basic or neutral zinc compound could be used but the oxides, hydroxides and carbonates are most often employed.
• Commercial additives frequently contain an excess of zinc due to the use of an excess of the basic zinc compound in the neutralization reaction.
• the preferred oil-soluble zinc dialkyldithiophosphates may be produced from dialkykyldithiophosphoric acids of the formula:
• the hydroxyl alkyl compounds from which the dialkyldithiophosphoric acids are derived can be represented generically by the formula ROH or R′OH, wherein R or R′ is alkyl or substituted alkyl, preferably branched or non-branched alkyl containing 3 to 30 carbon atoms. More preferably, R or R′ is a branched or non-branched alkyl containing 3 to 8 carbon atoms.
• hydroxyl alkyl compounds may also be used. These hydroxyl alkyl compounds need not be monohydroxy alkyl compounds.
• the dialkyldithiophosphoric acids may thus be prepared from mono-, di-, tri-, tetra-, and other polyhydroxy alkyl compounds, or mixtures of two or more of the foregoing.
• the zinc dialkyldithiophosphate derived from only primary alkyl alcohols is derived from a single primary alcohol.
• that single primary alcohol is 2-ethylhexanol.
• the zinc dialkyldithiophosphate derived from only secondary alkyl alcohols Preferably, that mixture of secondary alcohols is a mixture of 2-butanol and 4-methyl-2-pentanol.
• the phosphorus pentasulfide reactant used In the dialkyldithiophosphoric acid formation step may contain minor amounts of any one Or more of P 2 S 3 , P 4 S 3 , P 4 S 7 , or P 4 S 9 , Compositions as such may also contain minor amounts of free sulfur.
• lubricating oil compositions of the present invention are capable of providing excellent antiwear performance in the presence of amounts of zinc dialkyldithiophosphate providing greater amounts of phosphorus
• the improved performance of the inventive lubricating oil compositions are particular apparent in low SAPS formulations which, by definition, have phosphorus levels of no greater than about 0.08 wt. %. Therefore, lubricating oil compositions of the present invention contains less than about 0.08 wt. % of phosphorus, more preferably from about 0.03 to about 0.075 wt. % of phosphorus.
• An. exemplary lubricating oil composition of the present invention comprises about 11.5 mM zinc dialkyldithiophosphate.
• the viscosity index of the base stock is increased, or improved, by incorporating therein, certain polymeric materials that function as viscosity modifiers (VM) or viscosity index improvers (VII).
• VM viscosity modifiers
• VII viscosity index improvers
• polymeric materials useful as viscosity modifiers are those having number average molecular weights (Mn) of from about 5,000 to about 250,000, preferably from about 15,000 to about 200,000, more preferably from about 20,000 to 150,000 Daltons.
• viscosity modifiers can optionally be grafted with grafting materials such as, for example, maleic anhydride, and the grafted material can be reacted with, for example, amines, amides, nitrogen-containing heterocyclic compounds or alcohol, to form multifunctional viscosity modifiers (dispersant-viscosity modifiers).
• grafting materials such as, for example, maleic anhydride
• the grafted material can be reacted with, for example, amines, amides, nitrogen-containing heterocyclic compounds or alcohol, to form multifunctional viscosity modifiers (dispersant-viscosity modifiers).
• Exemplary lubricating oil compositions of the present invention employ various polyalkyl methacrylate copolymers, which may or may not be grafted by maleic anhydride.
• the copolymers may be employed at an amount from about 0.1 to about 10 wt. % of the lubricating oil composition.
• Lubricating oil compositions of the present invention further comprise a sulfur-containing molybdenum compound.
• Certain sulfur-containing organo-molybdenum compounds are known to function as friction modifiers in lubricating oil compositions, while also providing antioxidant and antiwear credits to a lubricating oil composition.
• oil soluble organo-molybdenum compounds include dithiocarbamates, dithiophosphates, dithiophosphinates, xanthates, thioxanthates, sulfides, and the like, and mixtures thereof.
• Oil-soluble or dispersible trinuclear molybdenum compounds can be prepared by reacting in the appropriate liquid(s)/solvent(s) a molybdenum source such as (NH 4 ) 2 Mo 3 S 13 n(H 2 O), where n varies between 0and 2 and includes non-stoichiometric values, with a suitable ligand source such as a tetralkylthiuram disulfide.
• a molybdenum source such as (NH 4 ) 2 Mo 3 S 13 n(H 2 O), where n varies between 0and 2 and includes non-stoichiometric values
• a molybdenum source such as of (NH 4) 2 Mo 3 S 13 .n(H 2 O)s a ligand source such as tetralkylthiuram disulfide, dialkyldithiocarbamate, or dialkyldithiophosphate, and a sulfur-abstracting agent such as cyanide ions, sulfite ions, or substituted phosphines.
• a trinuclear molybdenum-sulfur halide salt such as [M′] 2 [MO 3 S 7 A 6 ], where M′ is a counter ion, and A is a halogen such as Cl, Br, or I, may be reacted with a ligand source such as a dialkyldithiocarbamate or dialkyldithiophosphate in the appropriate liquid(s)/solvent(s) to form an oil-soluble or dispersible trinuclear molybdenum compound.
• the appropriate liquid/solvent may be, for example, aqueous or organic.
• oil-soluble or “dispersible” used herein do not necessarily indicate that the compounds or additives are soluble, dissolvable, miscible, or capable of being suspended in the oil in all proportions. These do mean, however, that they are, for instance, soluble or stably dispersible in oil to an extent sufficient to exert their intended effect in the environment in which the oil is employed. Moreover, the additional incorporation of other additives may also permit incorporation of higher levels of a particular additive, if desired.
• An exemplary lubricating oil composition of the present invention employs a molybdenum succinimide complex as friction modifier.
• the molybdenum complex may constitute from about 0.15 to about 0.55 wt. %, preferably from about 0.28 to about 0.45 wt. %.
• Oxidation inhibitors or antioxidants reduce the tendency of mineral oils to deteriorate in service.
• Such oxidation inhibitors include hindered phenols, alkaline earth metal salts of alkylphenolthioesters having preferably C 5 to C 12 alkyl side chains, calcium nonylphenol sulfide, oil soluble phenates and sulfurized phenates, phosphosulfurized or sulfurized hydrocarbons or esters, phosphorous esters, metal thiocarbamates, oil soluble copper compounds as described in, for example, U.S. Pat. No. 4,867,890.
• Aromatic amines having at least two aromatic groups attached directly to the nitrogen constitute another class of compounds that is frequently used for antioxidancy.
• Typical oil soluble aromatic amines having at least two aromatic groups attached directly to one amine nitrogen contain from 6 to 16 carbon atoms.
• the amines may contain more than two aromatic groups.
• the aromatic rings are often substituted by one or more substituents selected from, for example, alkyl, cycloalkyl, alkoxy, aryloxy, acyl, acylamino, hydroxy, and nitro groups.
• Lubricating oil compositions in accordance with the present invention preferably contain from about 0.05 to about 5,00 wt. %, more preferably from about 0.10 to about 3.00 wt. %. and particularly preferably from about 0.20 to about 0.80 wt. % of phenolic antioxidant, aminic antioxidant, or a combination thereof, based on the total weight of the lubricating oil composition.
• An exemplary lubricating oil composition of the present invention comprises about 0.40 wt. % of an antioxidant that is di-C 8 -diphenylamine.
• Another exemplary lubricating oil composition of the present invention comprises about 0.30 wt. % of a dinonyl diphenylamine as an antioxidant.
• Additional additives may be incorporated into the compositions of the invention to satisfy the particular performance requirements associated with low SAPS applications in internal combustion engines.
• additional additives include, for example, rust inhibitors, anti-foaming agents, and seal fixes or seal pacifiers.
• Rust inhibitor or anti corrosion agents may be a nonionic polyoxyethylene surface active agent.
• Nonionic polyoxyethylene surface active agents include, but are not limited to, polyoxyethylene lauryl ether, polyoxyethylene higher alcohol ether, polyoxyethylene nonylphenyl ether, polyoxyethylene octylphenyl ether, polyoxyethylene octyl stearyl ether, polyoxyethylene oleyl ether, polyoxyethylene sorbitol monostearate, polyoxyethylene sorbitol mono-oleate, and polyethylene glycol monooleate.
• Rust inhibitors or anticorrosion agents may also be other compounds, which include, for example, stearic acid and other fatty acids, dicarboxylic acids, metal soaps, fatty acid amine salts, metal salts of heavy sulfonic acid, partial carboxylic acid ester of polyhydric alcohols, and phosphoric esters.
• An exemplary lubricating oil composition of the present invention comprises a calcium stearate salt.
• Foam inhibitors typically include alkyl methacrylate polymers and dimethyl silicone polymers.
• Exemplary compositions of the present invention contain silicon-based foam inhibitors in amounts ranging from about 5 to about 40 ppm, preferably from about 8 to about 35 ppm, more preferably from about 10 to about 25 ppm, based on the total weight of the composition.
• Seal fixes are also termed seal swelling agents or seal pacifiers. They are often employed in lubricant or additive compositions to insure proper elastomer sealing, and prevent premature seal failures and leakages.
• Seal swell agents may be, for example, oil-soluble, saturated, aliphatic, or aromatic hydrocarbon esters such as di-2-ethylhexylphthalate, mineral oils with aliphatic alcohols such as tridecyl alcohol, triphosphate ester in combination with a hydrocarbonyl-substituted phenol, and di-2-ethylhexylsebacate.
• additives can provide a multiplicity of effects; thus for example, a single additive may act as a dispersant as well as an oxidation inhibitor. These multifunctional additives are well known.
• each additive is typically blended into the base oil in an amount that enables the additive to provide its desired function, it may be desirable, although not essential, to prepare one or more additive concentrates comprising additives (concentrates sometimes being referred to as additive packages) whereby several additives can be added simultaneously to the oil to form me lubricating oil composition.
• the final composition may employ from about 5 to about 30 wt. %, preferably about 5 to about 25 wt. %, typically about 10 to about 20 wt. % of the concentrate, the remainder being the oil of lubricating viscosity.
• the components can be blended in any order and can be blended as combinations of components.
• Oil A was prepared and tested for piston cleanliness and tendency to piston ring sticking according to the Volkswagen Turbocharged DI test, a European passenger car diesel engine test (CEL-L-78-T-99), which is part of the ACEA B specification promulgated by the European Automobile Manufacturers Association in 2004. This test was used to simulate repeated cycles of high-speed operation followed by idling.
• a Volkswagen 1.9 liter, inline, four-cylinder turbocharged direct injection automotive diesel engine (VW TDi) was mounted on an engine dynamometer stand.
• a 54-hour, 2-phased procedure that cycles between 30 minutes of 40° C. oil sump at idle and 150 minutes of 145° C. oil sump at full power (4150 rpm) was carried out without interim oil top-ups.
• Oil A shows a distinct and surprising improvement over Comparative Oil B in the VW TDi piston cleanliness and ring sticking test.
• a lubricating oil composition was prepared comprising about 1.50 wt. % of a polyisobutylene succinic anhydride derived from a polyisobutylene having a number average molecular weight of about 2300 Daltons, an ethylene carbonate-treated bissuccinimide dispersant, a low-overbased calcium sulfonate detergent, an overbased sulfurized and carbonated calcium phenate, a zinc dihydrocarbyl dithiophosphate, a moly succinimide, a di-C 8 -diphenylamine antioxidant, a silicon-based foam inhibitor, an ethylene polymer, a rust inhibitor, and mineral oil base stocks.
• a polyisobutylene succinic anhydride derived from a polyisobutylene having a number average molecular weight of about 2300 Daltons
• an ethylene carbonate-treated bissuccinimide dispersant a low-overbased calcium sulfonate detergent, an overbased sulfurized and carbon
• Oil A had a sulfated ash content of about 0.78 wt. %, nitrogen content of about 0.092 wt. %, sulfur content of about 0.183 wt. %, and phosphorus content of about 0.071 wt. %.
• Comparative Example Oil B the formulation of Oil A was duplicated except that Oil B does not contain PIBS A 2300. Oil B had a sulfated ash content of about 0.78 wt. %, nitrogen content of about 0.092 wt. %, sulfur content of 0.183 wt. %, and phosphorus content of 0.071 wt. %.
• VWTD12 SAE 5W30 Components Oil A Oil B PIBSA 2300 1.50 wt. % None Bissuccinimide dispersant 6.50 wt. % 6.50 wt. % Low-TBN calcium sulfonate 4 mM 4 mM Calcium Stearate 35 mM 35 mM High-TBN sulfurized & 10 mM 10 mM carbonated calcium phenate 11.5 mM 11.5 mM Zinc dialkyldithiophosphate 0.37 wt. % 0.37 wt. % Moly succinimide 0.40 wt. % 0.40 wt.
• ACEA B4 limits ACEA B5 limits P-MER Avg 63 ( ⁇ RL206-3) 66 ( ⁇ RL206) # Rngs w/ASF ⁇ 2.5 ⁇ 1.2 ⁇ 1.2 Grvs, 1st RStk, MX, ASF ⁇ 2.5 ⁇ 2.5 Grvs, 2nd Rstk, MX, ASF ⁇ 0.0 ⁇ 0.0
• Oil C was prepared and tested for piston cleanliness and tendency to piston ring sticking according to the Volkswagen Turbocharged DI test described above.
• the Piston cleanliness and ring sticking of VW TDi engine tests were also carried out with Comparative Example Oil D.
• the results are given in Table 3.
• the results were scored against the more stringent Japanese piston cleanliness standards (JASO C2 test standards), wherein the P-MER AVG has a minimum value of 65.
• Oil C shows a distinct and surprising improvement over Comparative Oil D In the VW TDi piston cleanliness and ring sticking test.
• a lubricating oil composition was prepared comprising about 2.00 wt. % of a succinic anhydride derivative of polyisobutylene having a number average molecular weight of about 2300, an ethylene carbonate-treated bissuccinimide dispersant that is a mixture of one derived from PIBSA 2300 and another derived from PIBSA 1300(i.e., the polyisobutylene precursor had a number average molecular weight of about 1300 Daltons), a low-overbased calcium sulfonate detergent, an overbased sulfurized and carbonated calcium phenate, a mixture of primary and secondary zinc dihydrocarbyl dithiophospbate, a moly succinimide, a triborate wear inhibitor, a viscosity improver, a di-C 8 -diphenylamine antioxidant, a silicon-based foam inhibitor, and mineral oil base stocks.
• Oil C had a sulfated ash content of about 0.59 wt. %, nitrogen content of about 0.113 wt. %, sulfur content of about 0.213 wt. %, and phosphorus content of 0.074 wt. %.
• Oil D The formulation of Oil C was duplicated except that Oil F did not contain PIBSA 2300.
• Oil D has a sulfated ash content of about 0.59 wt. %, nitrogen content of about 0.113 wt. %, sulfur content of 0.213 wt. %, and phosphorus content of 0,074 wt. %.
• VWTDI2 SAF 0W30 Components Oil C Oil D PIBSA 2300 2.00 wt. % None Bissuccinimide dispersant derived from 6.00 wt. % 6.00 wt. % PIBSA 2300 1.80 wt. % 1.80 wt. % Bissuccinimide dispersant derived from 7.5 mM 7.5 mM PIBSA 1300 17.5 mM 17.5 mM Low-TBN calcium sulfonate 12.0 mM 12.0 mM High-TBN sulfurized and carbonated 0.30 wt. % 0.30 wt. % calcium phenate 0.30 wt. % 0.30 wt.
• Zinc dialkyldithiophosphate mix 10 ppm 10 ppm Moly succinimide 0.20 wt. % 0.20 wt. % Dinonyl diphenylamine 5.80 wt. % 7.0 wt. % Silicon-based foam inhibitor 0.71 wt. % 0.71 wt.

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• 2006
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