JP2023517064A - Improved oxidation performance with sulfonate detergents - Google Patents

Abstract

A lubricating oil composition is provided. The composition contains several ingredients including a base oil, a primary antioxidant comprising an alkylated diphenylamine having an alkyl group derived from propylene tetramer, and a sulfonate detergent. [Selection drawing] Fig. 1

Description

CROSS REFERENCE TO RELATED APPLICATIONS This application entitled "IMPROVED OXIDATIVE PERFORMANCE WITH SULFONATE DETERGENTS" (Attorney Docket No.: T-11173) was filed March 11, 2020. US provisional application, the contents of which are incorporated herein by reference.

The present disclosure relates to lubricating oil additives that inhibit oxidation and extend the useful life of lubricating oils. More specifically, this disclosure relates to lubricating oil compositions comprising an alkylated diphenylamine antioxidant and a sulfonate detergent.

Oxidation is a concern for lubricating oils in use because it can cause oil thickening, sludge, varnish, acid number increase, and corrosion. These results are generally detrimental to proper operation of automobile engines and limit the useful life of the lubricant. With ever-evolving engine designs, operating conditions, and oil performance expectations, oxidation continues to be a significant technical challenge.

One way to retard engine oxidation is to introduce antioxidants into the lubricant. In addition, antioxidants can extend drain intervals, maintain viscosity, reduce deposits, reduce foam formation, protect against corrosion, and protect lubricants from high temperatures.

There are many antioxidants with varying degrees of effectiveness. Commercial lubricants are typically formulated with one or more antioxidants to protect the fluid under various conditions (eg, temperature, time, air mixture, pressure, etc.).

In particular, alkylated diphenylamines are used as antioxidants. Widely used alkylated diphenylamine antioxidants include nonylated (C9) diphenylamines that can be added to organic fluids such as engine oils, gear oils, hydraulic oils, compressor oils, turbine oils, and greases.

The present disclosure relates to lubricating oil additives that inhibit oxidation and extend the useful life of lubricating oils. More specifically, the disclosure relates to compositions comprising an alkylated diphenylamine and a sulfonate detergent.

In one aspect, lubricating oil compositions are provided comprising: a base oil, a primary antioxidant comprising an alkylated diphenylamine having an alkyl group derived from propylene tetramer, and a sulfonate detergent.

In a further aspect, a method is provided for improving the oxidative stability of a lubricating oil comprising the steps of: a base oil; a primary antioxidant comprising an alkylated diphenylamine having an alkyl group derived from propylene tetramer; supplying a lubricating oil composition comprising a detergent to an engine.

Figure 2 shows a comparison of the oxidation induction times of the blended oil samples described in the examples.

As used herein, the following words and expressions have the meanings ascribed below when and when used.

The term "antioxidant" or equivalent terms (eg, "oxidation stabilizer" or "oxidation inhibitor") refers to a composition and its ability to resist harmful attack in an oxidizing environment. Antioxidants are often used in organic fluids (eg, lubricating oils, gear oils, compressor oils, mineral oils, hydraulic oils) to improve the oxidative stability of organic fluids.

The term "alkyl" or related terms refers to a saturated hydrocarbon group, which may be linear, branched, cyclic, or a combination of cyclic, linear and/or branched.

The term "olefin" refers to a hydrocarbon having at least one carbon-carbon double bond that is not part of an aromatic ring or ring system. Olefins include aliphatic and aromatic, cyclic and acyclic, and/or linear and branched compounds having at least one carbon that is not part of an aromatic ring or ring system unless otherwise specified. It may contain compounds with double bonds in between. Olefins having only one, two, three, etc. carbon-carbon double bonds are identified by using the terms "mono", "di", "tri", etc. in the olefin name. obtain. Olefins can be further distinguished by the position of the carbon-carbon double bond(s). Depending on the context, the term "olefin" may refer to "olefin oligomer" or "olefin monomer" or both.

An "olefin oligomer" is an oligomer obtained by oligomerizing an "olefin monomer". For example, "propylene oligomer" is made from the oligomerization of propylene monomer. Examples of propylene oligomers include propylene tetramer and propylene pentamer. "Propylene tetramer" is an olefin oligomer product that nominally results from the oligomerization of four propylene monomers. These terms may also be used generically to refer to homo-oligomers, co-oligomers, salts of oligomers, derivatives of oligomers, and the like.

"Minor" or related term is expressed in terms of the stated additive and in terms of the total weight of the composition and means less than 50% by weight of the composition calculated as active ingredient of the additive.

"Major amount" or related term means an amount greater than 50% by weight based on the total weight of the composition.

BACKGROUND OF THE INVENTION 1. Field of the Invention This invention relates to antioxidant compositions that counteract oxidation and extend the useful life of lubricating oils. More specifically, the present invention describes antioxidant compositions comprising multiple lubricating oil additives. Lubricant additives include at least one antioxidant and at least one detergent that work together to improve oxidation performance. The improved performance is the result of a heretofore unknown synergistic effect resulting from the lubricating oil additive components of the present invention in lubricating oil compositions. Antioxidants and detergents compatible with the present invention are described herein.

Primary Antioxidant The antioxidant composition comprises a primary antioxidant and one or more secondary antioxidants. The primary antioxidants of the present invention are alkylated diphenylamines having one or more relatively long alkyl groups. Conventional alkylated diphenylamine antioxidants typically utilize relatively short alkyl groups. These include, for example, nonylated diphenylamines (“propylene trimers”) that nominally have nine carbons and can be formed from the oligomerization of propylene.

The alkylated diphenylamines of the present invention are alkylated with propylene tetramers (nominally having 12 carbons) or with mixtures containing propylene tetramers, the propylene tetramer being the predominant olefin oligomer alkylation. is an agent. Propylene tetramer can be obtained by oligomerization of four propylene monomers. Propylene tetramer has several potential advantages over propylene trimer, including but not limited to improved oil solubility, lower cost, and resistance to oxidation. stability.

The alkylated diphenylamines of the present invention comprise from about 0.4% to about 20%, such as from about 0.5% to about 15%, from 0.1% to about 10%, by weight of the lubricating oil composition, .5 wt % to about 8 wt %, or 1 wt % to about 5 wt %.

Propylene Oligomers The propylene oligomers (ie, propylene tetramers) of the present invention can be prepared by any compatible method known in the art. As an example, a process for preparing propylene oligomers uses a liquid phosphoric acid oligomerization catalyst. A description of this liquid phosphoric acid catalyzed propylene oligomerization process can be found in U.S. Pat. is incorporated herein by reference.

The crude product of the oligomerization process typically contains a mixture of branched olefins with a distribution of carbon numbers. In commercial settings, olefin oligomers are subjected to extreme conditions during the oligomerization process, resulting in cracking, recombination, isomerization, and the like. A purified or processed oligomerization product usually has a higher concentration of the desired product. Accordingly, the term "propylene tetramer" does not necessarily refer to a pure propylene tetramer product, but may also refer to a mixture of olefin or olefin oligomer products. Thus, alkylation products, including diphenylamine and propylene tetramer, can have a distribution of carbon numbers within the alkylated alkyl group.

Propylene tetramer may be obtained from the oligomerization of four propylene monomers. Propylene tetramer is cost effective for producing olefins. Characterized by highly branched chains of 10-15 carbons and a high degree of methyl branching as products of oligomerization, imparting excellent oil solubility and compatibility with other oil soluble lubricating oil additive components . In some embodiments, the average carbon number may range from about 10 to about 15.

The products of oligomerization can differ in the degree of branching. For example, a propylene tetramer can exhibit total branching (ie, the sum of olefinic and aliphatic branching) ranging from 1 to 15. In some embodiments, the average total branching can range from about 1 to about 15.

Propylene tetramers of the present invention generally contain at least 50% by weight of C ₁₀ -C ₁₅ carbon atoms. In one embodiment, the propylene tetramer comprises a carbon atom distribution comprising at least 60% by weight of C ₁₀ -C ₁₅ carbon atoms. In one embodiment, the propylene tetramer comprises a carbon atom distribution comprising at least 70% by weight of C ₁₀ -C ₁₅ carbon atoms. In one embodiment, the propylene oligomer comprises a carbon atom distribution comprising at least 80% by weight of C ₁₀ -C ₁₅ carbon atoms. In one embodiment, the propylene oligomer comprises a carbon atom distribution comprising at least 90% by weight of C ₁₀ -C ₁₅ carbon atoms.

As will be apparent to those skilled in the art, propylene oligomers as used herein may also include minor amounts of lower molecular weight propylene oligomer(s), such as propylene trimer, and higher molecular weight propylene oligomer(s). , for example, propylene pentamer. For example, the propylene tetramer of the present invention contains 0-1 _wt .% C ₉ H ₁₈ , 0-5 _wt .% C ₁₀ H ₂₀ , 0-10 wt. a mixture of olefinic hydrocarbons comprising C ₁₂ H ₂₄ , 10-20 wt % C ₁₃ H ₂₆ , 5-15 wt % C ₁₄ H ₂₈ , and/or 1-10 wt % C ₁₅ H ₃₀ good too.

Alkylation The alkylated diphenylamines of the invention may be obtained by any alkylation process compatible with the invention. For example, US Pat. No. 6,355,839, incorporated herein by reference, describes the preparation of alkylated diphenylamines in which diphenylamine is alkylated with polyisobutylene.

Any suitable catalyst may be used. For example, alkylation of diphenylamine can proceed in the presence of clay catalysts. The temperature of this reaction may range from 140°C to 200°C, more typically from 150°C to 190°C. In some embodiments, the reaction temperature ranges from 160°C to 180°C. The reaction may be performed at a single temperature or may be performed at different temperatures sequentially. Propylene oligomers are charged at a charge mole ratio (CMR) of 2:1 to 8:1 relative to the diphenylamine charge. In some embodiments, the CMR is 3:1 to 7:1 or 4:1 to 6:1. The reaction product may be filtered to remove catalyst and then distilled to remove unreacted olefin oligomers and diphenylamine. The use of clay as a catalyst is disclosed in US Pat. No. 3,452,056, incorporated herein by reference.

As one skilled in the art would expect, reaction conditions may vary significantly depending on the catalyst used. For example, reactions with homogeneous acid catalysis may only require temperatures in the range of 75°C to 100°C.

Depending on the reaction conditions, the alkylated diphenylamine product can have varying relative amounts of mono-, di-, and/or tri-alkylated diphenylamine products. It should be apparent that for a given dialkylated or trialkylated diphenylamine molecule, the two or more alkylated alkyl groups can be the same or different according to this disclosure.

Secondary Antioxidants The present invention employs one or more secondary antioxidants in combination with the primary antioxidant. Secondary antioxidants are from about 0.01% to about 20% by weight of the lubricating oil composition, such as from about 0.05% to about 15%, from 0.1% to about 10%, It may be present from 0.5% to about 8% by weight, or from 1% to about 5% by weight.

Many secondary antioxidants are compatible with the present invention. Examples of secondary antioxidants include molybdenum succinimides, dithiocarbamates, and hindered phenols. These oil-soluble ingredients are generally known.

For example, mono- and polysuccinimides that can be used to prepare the molybdenum complexes described herein are disclosed in numerous references and are well known in the art. Certain basic types of succinimides and related substances included in the technical term "succinimide" are described in U.S. Pat. Nos. 3,219,666, 3,172,892; and US Pat. No. 3,272,746. The term "succinimide" is understood in the art to include many of the amide, imide and amidine species that may be formed. However, the major product is succinimide, a term generally accepted to mean the reaction product of an alkenyl-substituted succinic acid or anhydride and a nitrogen-containing compound.

Preferred succinimides, due to their commercial availability, are succinimides prepared from hydrocarbyl succinic anhydrides in which the hydrocarbyl group contains from about 24 to about 350 carbon atoms, and ethylene amines, the ethylene amines being particularly Characterized by ethylenediamine, diethylenetriamine, triethylenetetramine, and tetraethylenepentamine. Particularly preferred are succinimides prepared from polyisobutenylsuccinic anhydrides of 70 to 128 carbon atoms and tetraethylenepentamine or triethylenetetramine or mixtures thereof.

The term "succinimide" also includes co-oligomers of hydrocarbyl succinic acids or anhydrides and polysecondary amines containing two or more secondary amino groups plus at least one tertiary amino nitrogen. Generally, the average molecular weight of this composition is from 1,500 to 50,000. A typical compound would be prepared by reacting polyisobutenylsuccinic anhydride with ethylene dipiperazine.

Succinimides having an average molecular weight of 1000 or 1300 or 2300 and mixtures thereof are most preferred. Such succinimides may be post-treated with boron or ethylene carbonate as is known in the art.

Suitable dithiocarbamates include, but are not limited to, dithiocarbamates where the metal is zinc, copper, or molybdenum, ashless thiocarbamates, or dithiocarbamates (i.e., essentially metal-free) such as methylenebis ( dialkyldithiocarbamates), ethylenebis(dialkyldithiocarbamates), and isobutyl disulfide-22′-bis(dialkyldithiocarbamates), the alkyl groups of the alkyldithiocarbamates preferably having 1 to 6 carbon atoms. . Examples of preferred ashless dithiocarbamates are methylenebis(dibutyldithiocarbamate), ethylenebis(dibutylthiocarbamate) and isobutyldisulfide-2,2'-bis(dibutyldithiocarbamate).

A secondary antioxidant used in the lubricating oils of the present invention may be a sterically hindered phenol. Hindered phenol antioxidants often contain secondary and/or tertiary butyl groups as sterically hindering groups. Phenolic groups are often further substituted with hydrocarbyl groups and/or bridging groups (which link to a second aromatic group). Suitable hindered phenols include, but are not limited to, 2,6-di-tert-butylphenol, 4-methyl-2,6-di-tert-butylphenol, 4-ethyl-2,6-di-tert -butylphenol, 4-propyl-2,6-di-tert-butylphenol or 4-butyl-2,6-di-tert-butylphenol, or 4-dodecyl-2,6-di-tert-butylphenol.

Detergents The antioxidant compositions of the present invention comprise one or more detergents. Detergents are from about 0.01% to about 10% by weight of the lubricating oil composition, such as from about 0.05% to about 8%, from 0.1% to about 5%, from 0.5% It may be present in weight percent to about 4 weight percent, or 1 weight percent to about 3 weight percent.

Detergents are usually salts (e.g., overbased salts) and are characterized by excess metal content, which may be present depending on the stoichiometry of the metal and the particular acidic organic compound reacted with the metal. It is a phase homogeneous Newtonian system.

The detergents of the present invention include sulfonate detergents. Metal detergents, such as sulfonate detergents, typically contain a polar head and a hydrocarbon tail or lipophilic group. Generally, the hydrocarbon tail can range from about 3 carbons to 50 carbons in length.

Sulfonate detergents can be natural or synthetic. Detergents can be neutral or overbased. Overbased detergents may vary in degree of overbasing (as measured by ASTM D2896). Suitable overbased sulfonates include low overbased, medium overbased, high overbased, and high overbased sulfonate detergents. In some embodiments, the detergent can be borated.

Examples of sulfonate detergents include alkylaryl sulfonates and the like. Specific examples include magnesium alkyltoluenesulfonates described in US20110136711. Other examples include calcium alkylarylsulfonates, calcium alkyltoluenesulfonates, and magnesium alkylbenzenesulfonates.

Detergent metals also include alkali or alkaline earth metals such as barium, sodium, potassium, lithium, calcium, and magnesium. The most commonly used metals are calcium and magnesium, both of which can be present in detergents used in lubricants and mixtures of calcium and/or magnesium with sodium.

In some embodiments, additional cleaning agents may be used. Additional detergents include phenates, salicylates, phenolates, phosphonates, thiophosphonates, ionic surfactants, and the like. In some embodiments, additional detergents include hybrid and/or complex detergents.

Lubricating Oil Compositions The antioxidant compositions of the present disclosure may be used in lubricating oils to impart oxidative stability to the lubricating oils. The primary antioxidant, secondary antioxidant, and one or more detergents can be present in any ratio as long as their concentrations fall within the guidelines provided herein.

In general, antioxidant compositions are oil-soluble, e.g., being able to dissolve or stably disperse in oil to a sufficient degree to exert their intended effect in the environment in which the oil is used. means Additionally, higher levels of a particular additive can be incorporated by further incorporating other additives, if desired. The term oil-soluble does not necessarily indicate that the compound or additive is soluble, dissolvable, miscible or suspendable in oil in all proportions. If other antioxidants are present in the lubricating oil composition, lesser amounts of the antioxidants of the present invention may be used.

The oil used as the base oil is selected or blended depending on the desired end use and additives in the finished oil to obtain the desired grade of engine oil, such as 0W, 0W-8, 0W-16, 0W. -20, 0W-30, 0W-40, 0W-50, 0W-60, 5W, 5W-20, 5W-30, 5W-40, 5W-50, 5W-60, 10W, 10W-20, 10W-30 , 10W-40, 10W-50, 15W, 15W-20, 15W-30, or 15W-40 Society of Automotive Engineers (SAE) viscosity grades are obtained. Straight grade base oils such as SAE 30, 40, 50, and 60 can also be used.

Oils of lubricating viscosity (sometimes referred to as "base stocks" or "base oils") are the primary liquid component of lubricants, and are blended with additives and possibly other oils to form e.g. A lubricant (or lubricant composition) is produced. Useful base oils for making concentrates and for making lubricating oil compositions therefrom are selected from natural (vegetable, animal or mineral) and synthetic lubricating oils and mixtures thereof. can be

The definitions of base stock and base oil in this disclosure are set forth in the American Petroleum Institute (API) Publication 1509 Annex E ("API Base Oil Interchangeability Guidelines for Passenger Car Motor Oils and Diesel Engine Oils 2 6"). same as is. Group I basestocks contain less than 90% saturated sulfur and/or greater than 0.03% sulfur and have a viscosity index greater than or equal to 80 and less than 120 using the test methods set forth in Table E-1. Group II basestocks contain greater than or equal to 90% saturated sulfur and less than or equal to 0.03% sulfur and have a viscosity index greater than or equal to 80 and less than 120 using the test method set forth in Table E-1. Group III basestocks contain 90% or more saturated sulfur, 0.03% or less sulfur, and have a viscosity index of 120 or more using the test method set forth in Table E-1. Group IV basestocks are polyalphaolefins (PAO). Group V base stocks include all other base stocks not included in Groups I, II, III, or IV.

Natural oils include animal oils, vegetable oils (eg, castor oil and lard oil), and mineral oils. Animal and vegetable oils with favorable thermo-oxidative stability may be used. Of the natural oils, mineral oils are preferred. Mineral oils vary widely with respect to their crude source, eg, whether they are paraffinic, naphthenic, or mixed paraffinic-naphthenic. Oils derived from coal or shale are also useful. Natural oils also describe the methods used in their production and refining, such as their distillation range, and whether they are straight run, cracked, or hydrorefined. , or an extracted solvent.

Synthetic oils include hydrocarbon oils. Hydrocarbon oils include oils such as polymerized and interpolymerized olefins (eg, polybutylene, polypropylene, propylene isobutylene copolymers, ethylene-olefin copolymers and ethylene-alpha olefin copolymers). Polyalphaolefin (PAO) oil base stocks are commonly used for synthetic hydrocarbon oils. By way of example, PAOs derived from C ₈ -C ₁₄ olefins, such as C ₈ , C ₁₀ , C ₁₂ , C ₁₄ olefins, or mixtures thereof may be utilized.

Other useful fluids for use as base oils include non-conventional or unconventional base stocks that have preferably been catalytically treated or synthesized to provide high performance properties. .

Non-conventional or non-conventional base stocks/base oils include mixtures of base stock(s) derived from one or more gas-to-liquid (GTL) materials, as well as those derived from natural waxes or waxy feedstocks. Isomerized/isodewaxed base stock(s), mineral oil and/or non-mineral oil waxy feedstocks such as slack wax, natural waxes and wax stocks such as gas oils, waxy fuel hydrocracker bottoms, waxes Raffinates, hydrocracates, pyrocrackates, or other mineral, mineral oil, and non-petroleum derived waxy materials, such as waxy materials received from coal liquefaction or shale oil, as well as mixtures of such basestocks One or more.

Base oils for use in the lubricating oil compositions of the present disclosure include API Group I, Group II, Group III, Group IV and Group V oils, and mixtures thereof, preferably API Group II, Group III, Any of the various oils corresponding to Group IV and Group V oils and mixtures thereof, more preferably Group III to Group V base oils (their outstanding volatility, stability, viscosity measurement and cleanliness due to the characteristics).

Typically, the base oil has a viscosity of 2.5 to 20 mm ² /s (eg 3 to 12 mm ² /s, 4 to 10 mm ² /s, or 4.5 to 8 mm ² /s) at 100°C. of kinetic viscosity (ASTM D445).

The lubricating oil compositions may also contain conventional lubricant additives to provide auxiliary functions, resulting in a finished lubricating oil composition in which these additives are dispersed or dissolved. For example, the lubricating oil composition may contain antioxidants, ashless dispersants, antiwear agents, detergents such as metal detergents, rust inhibitors, dehazing agents, demulsifiers, friction modifiers, metal deactivators. agents, pour point depressants, viscosity modifiers, defoamers, co-solvents, package compatibility agents, corrosion inhibitors, dyes, extreme pressure additives, etc., and mixtures thereof. Various additives are known and commercially available. These additives, or their analogous compounds, may be used in preparing the lubricating oil compositions of this invention by conventional blending procedures.

Each of the foregoing additives, when used, are used in functionally effective amounts to impart desired properties to the lubricant. Thus, for example, if the additive is an ashless dispersant, a functionally effective amount of the ashless dispersant is an amount sufficient to impart the desired dispersant characteristics to the lubricant. Generally, the concentration of each of these additives when used may range from about 0.001 to about 20 weight percent, such as from about 0.01 to about 10 weight percent, unless otherwise specified. .

The following illustrative examples are intended to be non-limiting.

EXAMPLES Fully formulated engine oils were tested for oxidation induction time as shown in FIG. Fully formulated engine oils contain one or more antioxidants and sulfonate detergents, as well as common lubricating oil additives such as dispersants and corrosion inhibitors.

A first engine oil sample ("DPA only") contains a sulfonate detergent and an alkylated diphenylamine. Alkylated diphenylamine is nonylated diphenylamine or diphenylamine (alkylated with propylene tetramer). Gas chromatographic analysis of diphenylamine alkylated with propylene tetramer is summarized in Table 1 below. This analysis indicates that approximately half of the sample is monoalkylated diphenylamine. The other half of the sample is dialkylated diphenylamine. Diphenylamines with C3-C8 alkyl groups are present in very small amounts.

Other engine oil samples contained one or more additional antioxidants (ie molybdenum succinimides, hindered phenols, dithiocarbamates). In blended engine oil samples containing multiple antioxidants, each antioxidant present is present at equivalent treat levels/weight percent.

Test engine oil samples featuring two antioxidants included alkylated diphenylamines and molybdenum succinimide ("DPA/Mosuccinimide"), hindered phenols ("DPA/hindered phenols") or dithiocarbamates ("DPA/Mosuccinimides"). DPA/dithiocarbamates"). Test engine oil samples featuring three antioxidants included alkylated diphenylamines, molybdenum succinimide and hindered phenol ("DPA/Mosuccinimide/hindered phenol"), molybdenum succinimide and dithiocarbamate ("DPA/ Mo succinimide/dithiocarbamates"), or hindered phenols and dithiocarbamates ("DPA/hindered phenols/dithiocarbamates"). A test engine oil sample featuring four antioxidants included alkylated diphenylamines, molybdenum succinimides, hindered phenols, and dithiocarbamates ("DPA/Mosuccinimide/hindered phenols/dithiocarbamates"). be

For each test sample, the sulfonate detergents (low and medium overbased sulfonates) are present at 78 mM, while the total concentration of antioxidant(s) is 1.5% by weight.

The data show consistently higher oxidation induction times for samples containing diphenylamine alkylated with propylene tetramer compared to samples containing nonylated diphenylamine.

Oxidation induction time was evaluated using pressure differential scanning calorimetry (PDSC) according to ASTM D6186 test protocol. Longer oxidation induction times indicated improved oxidation stability.

Claims (20)

A lubricating oil composition,
base oil,
a primary antioxidant comprising an alkylated diphenylamine having an alkyl group derived from propylene tetramer;
and said lubricating oil composition comprising a sulfonate detergent. 2. The lubricating oil composition of claim 1, further comprising a secondary antioxidant comprising a dithiocarbamate, hindered phenol, or molybdenum succinimide. 2. The lubricating oil composition of claim 1, wherein at least 50% of said alkyl groups of said alkylated diphenylamine have between 10 and 15 carbon atoms. 2. The lubricating oil composition of claim 1, wherein said sulfonate detergent is a petroleum-based detergent or a synthetic detergent. The lubricating oil composition according to claim 1, wherein said primary antioxidant is present at 0.01% to 20% by weight of said lubricating oil composition. 2. The lubricating oil composition of claim 1, wherein said sulfonate detergent is overbased. The lubricating oil composition according to Claim 1, wherein said secondary antioxidant is present at 0.01% to 20% by weight of said lubricating oil composition. The lubricating oil composition of claim 1, wherein the sulfonate detergent is present at 0.01% to 10% by weight of the lubricating oil composition. 2. The lubricating oil composition of claim 1, further comprising:
Antioxidants, ashless dispersants, antiwear agents, detergents, rust inhibitors, dehazing agents, demulsifiers, friction modifiers, metal deactivators, pour point depressants, viscosity modifiers , defoamers, co-solvents, package compatibility agents, corrosion inhibitors, pigments, or extreme pressure additives. 2. The lubricating oil composition of claim 1, wherein the sulfonate detergent comprises an internal olefin sulfonate, an alkyl ether sulfonate, an alcohol ether sulfonate, a linear alkylaryl sulfonate, or an alkane sulfonate. thing. A method for improving the oxidation stability of a lubricating oil, comprising:
a base oil;
a primary antioxidant comprising an alkylated diphenylamine having an alkyl group derived from propylene tetramer;
providing the engine with a lubricating oil composition comprising a sulfonate detergent. 12. The method of claim 11, wherein the lubricating oil composition further comprises:
The above method comprising a secondary antioxidant comprising a dithiocarbamate, hindered phenol, or molybdenum succinimide. 12. The method of claim 11, wherein at least 50% of said alkylated diphenylamines have 10-15 carbon atoms. 12. The method of claim 11, wherein the sulfonate detergent is a petroleum-based detergent or a synthetic detergent. 12. The method of claim 11, wherein said primary antioxidant is present at 0.01% to 20% by weight of said lubricating oil composition. 12. The method of claim 11, wherein the sulfonate detergent is overbased. 12. The method of claim 11, wherein said secondary antioxidant is present at 0.01% to 20% by weight of said lubricating oil composition. 12. The method of claim 11, wherein the sulfonate detergent is present at 0.01% to 10% by weight of the lubricating oil composition. 12. The method of claim 11, wherein the lubricating oil composition further comprises
Antioxidants, ashless dispersants, antiwear agents, detergents, rust inhibitors, defogging agents, demulsifiers, friction modifiers, metal deactivators, pour point depressants, viscosity modifiers, antifoam agents , co-solvents, package compatibility agents, corrosion inhibitors, pigments, or extreme pressure additives. 12. The method of claim 11, wherein the sulfonate detergent comprises an internal olefin sulfonate, an alkyl ether sulfonate, an alcohol ether sulfonate, a linear alkylaryl sulfonate, or an alkane sulfonate.

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