Low SAP engine lubricant additive and composition containing non-corrosive sulfur and organic borates

The present invention is directed to a lubricating oil composition comprising a lubricating oil basestock, a boron-containing additive of at least 0.1 weight percent of the composition and less than 8.0 weight percent, and ashless sulfur additive of at least 0.1 weight percent of the composition and less than 4.0 weight percent, a dispersant-detergent-inhibitor system of less than 15 percent weight percent of the composition, a zinc dithiophosphate additive of at least 0.2 weight percent of the composition and less than 2.0 weight percent of the composition. The elements in the formulated oil composition having at least 100 and less than 630 PPM phosphorus, at least 1,000 PPM and less than 3,000 PPM, at least 100 and less than 630 ppm Phosphorous, and at least 105 PPM and less than 710 PPM zinc. In a second embodiment, an additive composition for lubricating oils is disclosed. In a third embodiment, a method to obtain favorable lubricating properties is disclosed.

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Description
This application claims benefit of Provisional Application 60/791,775 filed Apr. 13, 2006. BACKGROUND OF THE INVENTION

1. Field of the Invention

This invention relates to lubricating oil compositions suitable for use in internal combustion engines. More particularly, this invention relates to a low ash, sulfur, and phosphorous lubricating oil composition.

2. Background

Many means have been employed to reduce overall wear and friction as well as to control oxidation/cleanliness in modern engines, particularly automobile engines. The primary methods include prolonging engine life by reducing engine wear and increasing the resistance to oxidation by reducing the engine's sludge/deposit build-up through oil degradation. Some of the solutions to reducing wear have been strictly mechanical including building engines with wear resistant alloy or ceramic parts, modifying the contact geometry and adding special coating materials. Solutions to improve cleanliness also involve modification of oil, including the use of metal containing detergents. Recently, considerable work has also been done with lubricating oils to enhance their anti-wear/anti-oxidation properties by modifying them with ashless antioxidants and anti-wear components.

Contemporary lubricants such as engine oils use mixtures of additive components to include numerous performances benefits. Examples of additives components include, anti-wear and extreme pressure components, fuel economy improving components, friction reducers, dispersants, detergents, corrosion inhibitors and viscosity index improving additive. These additives provide energy conservation, engine cleanliness and durability and high performance levels to the lubricating oil under a wide range of engine operability conditions including temperature, pressure and lubricant service life.

Throughout the world, legislation aimed at reducing automotive emissions is forcing down the level of sulfur in fuels. Recently, lubricants are coming under scrutiny as a source of air pollution and emission catalyst deactivation. Phosphorus is known to be poisonous to automotive three-way HC conversion catalysts.

Conventional engine oil technology relies heavily on zinc (dialkyl) dithiophosphate (“ZnDTP” or “ZDDP”). ZnDTP is a versatile, anti-wear/anti-oxidant component that provides extremely low cam and lifter wear and favorable oxidation protection under severe conditions. ZnDTPs are disadvantageous, especially at high treat rates because they carry the three disfavorable elements of Zn, S, P and no reduction in phosphorus and zinc levels can be realized until new additive technology permits replacing or eliminating zinc dithiophosphates. Sulfur is known to be poisonous to deNox catalysts and zinc phosphates cause plugging of the exhaust particulate filters. The sulfur, ash and phosphorous components in oil are commonly referred to as “SAP” or “SAPS” in the art.

The major problem with ZnDTP is the poisoning effects to after-treatment devices that may aggravate emission problems. In addition, ZnDTP has strong interactions with dispersants, detergents, other anti-wear components and MoDTC causing antagonistic effects on friction, sludge and deposit, if inappropriate concentrations are utilized. Replacing ZnDTP additives is not a simple endeavor because the wear protection demand for today's engine is extremely high and place extremely rigorous chemical limits on any reductions in ZnDTP treat levels.

Engine lubricating oils are often used in high temperature applications, where extreme temperatures can significantly reduce the useful life of the lubricant. Under high temperatures, the lubricant can become oxidized prematurely unless a strong antioxidant system can also be employed in the oil to prevent this degradation process. Good piston, ring, cam and lifter wear protection are also an important characteristic of today's engine oil. Additionally, many engine oils are often required to perform well in the presence of water, therefore, protecting against rust formation. Traditionally, ZnDTPs are used to provide adequate protection as described above. Engine designers are now requiring even greater anti-wear protection and more demanding test protocols are being put in place to insure that lubricants can meet these more stringent specifications. However, stringent regulations in emission control have forced lubricant formulators to move away from ZnDTPs for the reasons discussed above.

Accordingly, there is a need for an additive or additive system for engine oils that has the ability to improve both rust and wear protection, and at the same time significantly enhance oxidative stability, while meeting stringent emission requirements. This invention satisfies that need.

SUMMARY OF THE INVENTION

In a first embodiment, a lubricating oil composition is disclosed. This composition comprises a lubricating oil basestock, a boron-containing additive present in the amount in the range of at least 0.1 weight percent of the composition and less than 8.0 weight percent, a non-corrosive sulfur additive present in the amount in the range of at least 0.1 weight percent of the composition and less than 4.0 weight percent, a dispersant-detergent-inhibitor system of less than 15 percent weight percent of the composition, a zinc dithiophosphate additive present in the amount in the range of at least 0.2 weight percent of the composition and no more than 2.0 weight percent of the composition wherein weight percent is active ingredient weight of the composition. The formulated oil composition having at least 100 and less than 630 PPM phosphorus, at least 1,000 PPM and less than 3,000 PPM sulfur, and at least 105 PPM and less than 710 PPM zinc, at least 80 PPM and less than 450 PPM boron.

In a second embodiment, an additive composition for lubricating oils is disclosed. This composition comprises an organic boron containing additive present in the amount in the range of at least 0.4 weight percent and less than 32 weight percent of the additive, a detergent-dispersant system of less than 60 percent weight percent of the additive, a zinc dithiophosphate additive present in the amount in the range of at least 0.8 weight percent and less than 8.0 weight percent of the additive, a non-corrosive ashless sulfur additive present in the amount in the range of at 0.4 and less than 16.0 weight percent of the additive.

In a third embodiment, a method of obtain a favorable lubricating properties is disclosed. This method, comprises obtaining a composition comprising a lubricating oil basestock, an organic boron containing additive of at least 0.1 and less than 8 weight percent of the composition, a dispersant-detergent-inhibitor system of less than 15 percent weight percent of the composition, zinc dithiophosphate additive of at least 0.2 weight percent of the composition and no more than 2.0 weight percent of the composition, a non corrosive ashless sulfur additive of at 0.1 and less than 4.0 weight percent of the composition. The formulated oil composition having at least 100 and less than 630 PPM phosphorus, at least 1,000 PPM and less than 3,000 PPM sulfur, and at least 105 PPM and less than 710 PPM zinc, at least 80 PPM and less than 450 PPM boron.

DETAILED DESCRIPTION OF THE INVENTION

This invention relates to engine lubricants formulated with unique functional fluids and/or additives to achieve performance improvements. One embodiment is a low SAP engine lubricant composition comprising combinations of organic borates, non-corrosive sulfur compounds, optional high levels of ashless antioxidants, and low levels of ZnDTP to achieve high level of performance equal to or better than using high level of ZnDTP alone. In one embodiment, component synergy is built upon a variety of functionalities to achieve well balanced performance features. In a preferred embodiment, these performance features favorably exceed engine oils formulated with high levels of zinc dithiophosphates and metallic detergents.

In a second embodiment, the lubricating oils maintain low frictional properties of film under various operating conditions. This embodiment favorably maintains sufficiently high film thickness at high operating temperatures to provide a minimum lubricant film to protect against wear at a variety of temperatures.

In a third embodiment, the lubricating oil maintains cleanliness over the entire range of operating conditions while reducing wear to a minimum. In a fourth embodiment, the lubricating oil provides favorable oxidation and corrosion control, under the most severe operating conditions.

It has been discovered that non-corrosive, organic sulfur compounds when blended with high levels of organic borates, and low level of zinc dithiophosphates provide substantial property benefits. In a preferred embodiment, high levels of ashless antioxidants are added to the compounds to achieve even more favorable-property benefits. These benefits include but are not limited to reductions in wear, corrosion, and increases in oil induction temperature or time (OIT) during oxidative conditions that result in potentially significant improvements in engine oil service life and durability with excellent overall performance benefits. In an additional embodiment, these benefits can be achieved without deleterious effects such as instability, undesirable high viscosity, deposits and the like, when the additives are added to lubricating oils. This new engine oil technology is based on an advanced anti-wear, anti-friction and antioxidant system, in combination of some typical, contemporary dispersants, ashless antioxidants, detergents, defoamants and other additives including contemporary DI additive packages. These additives enhance anti-wear, anti-oxidation and anti-corrosion performance.

Persons skilled in the art with the benefit of the disclosure herein will recognize the ability to include additives that favorably enhances lubricant performance including anti-friction, anti-oxidation and anti-wear performance while successfully meeting the stringent wear, oxidation and cleanliness performance requirements in modern engines. Examples of suitable additives include but are not limited to contemporary zinc dithiophosphates in low levels, borated or non-borated dispersants, phenolic and aminic ashless anti-oxidants, high and low levels of metal detergents, molybdenum or organic friction modifiers, defoamants, seal swell additives, pour point depressants including contemporary DDI additive packages, and any combination thereof.

The preferred organic borates are borated hydroxyl esters, such as borated glycerol mono-oleate (GMO), borated glycerol di-oleate (GDO), borated glycerol tri-oleate (GTO), borated glycerol mono-cocoate (GMC), borated mono-talloate (GMT), borated glycerol mono-sorbitate (GMS), borated polyol esters with pendant hydroxyl groups, such as borated pentaerythritol di-C8 ester, and any combination thereof. Short chain tri-hydroxyl orthoborates may be used but are not desirable due to their relatively poor thermal/oxidative stability properties when compared to borated hydroxyl esters. Borated dispersants and borated detergents can be used as a source of boron. However, in order to achieve best overall performance, specific organic borates, such as borated hydroxyl esters are more preferable.

The preferred non-corrosive sulfur compounds are chosen from the group consisting of ashless derivatives of thiadiazoles, ashless derivatives of benzothiazoles, ashless alkyl or aryl sulfides and poly sulfides, for example, di-sulfides and tri-sulfide including thianthrene and its alkylates, diphenyl sulfide and disulfide, and their alkylates, dinonyl sulfide or disulfide, dipyridyl sulfide or disulfide, and their alkylates, ashless dithiocarbamates, and thioesters/sulfurized esters including thioglycolates, dialkyl thiodipropionates, dialkyl dithiopropionates. Examples of ashless thiadiazoles are Vanlube 871™, Cuvan 826™ and Cuvan 484™. Examples of ashless dithiocarbamates are Vanlube 7723™ and Vanlube 981. A prerequisite to the selection of sulfur additives is that they all need to meet copper corrosion requirements according to ASTM (D130) and low temperature storage compatibility tests.

The anti-corrosion performance can be judged by the copper corrosion test ASTDM D130 under normal conditions. For ASTDM test D130-6 normal conditions are at 250 degrees Fahrenheit at 3 hours. For ASTDM test D130-8, normal conditions are set at 210 degrees Fahrenheit for 6 hours with percent water, as well as a more severe condition at 250 degrees Fahrenheit for 24 hours. For purposes of this invention, non-corrosive sulfur shall be defined as any sulfur that provides a performance classification of 2B or better under the ASTM D-130 Copper Corrosion Test.

Dibenzyl disulfide was deficient in a severe copper corrosion test at degrees Fahrenheit for 24 hours and 2,2′-dipyridyl disulfide has poor low temperature compatibility in engine oils. Therefore, both additives are deemed less favorable, despite of their strong EP performance. Sulfur additives containing a small portion of polysulfides (tri-sulfide/tetra-sulfide and higher order of polysulfides) are still acceptable providing that they could meet the copper corrosion requirements.

The preferred ashless antioxidants are hindered phenols and arylamines. Typical examples are butylated/octylated/styrenated/nonylated/dodecylated diphenylamines, 4,4′-methylene bis-(2,6-di-tert-butylphenol), 2,6-di-tert-butyl-p-cresol, octylated phenyl-alpha-naphthylamine, alkyl ester of 3,5-di-tert-butyl-4-hydroxy-phenyl propionic acid, and many others. Sulfur-containing antioxidants, such as sulfur linked hindered phenols and thiol esters can also be used.

Suitable dispersants include borated and non-borated succinimides, succinic acid-esters and amides, alkylphenol-polyamine coupled Mannich adducts, other related components and any combination thereof. In some embodiments, it can often be advantageous to use mixtures of such above described dispersants and other related dispersants. Examples include additives that are borated, those that are primarily of higher molecular weight, those that consist of primarily mono-succinimide, bis-succinimide, or mixtures of above, those made with different amines, those that are end-capped, dispersants wherein the back-bone is derived from polymerization of branched olefins such as polyisobutylene or from polymers such as other polyolefins other than polyisobutylene, such as ethylene, propylene, butene, similar dispersants and any combination thereof. The averaged molecular weight of the hydrocarbon backbone of most dispersants, including polyisobutylene, is in the range from 1000 to 6000, preferably from 1500 to 3000 and most preferably around 2200.

Suitable detergents include but are not limited to calcium phenates, calcium sulfonates, calcium salicylates, magnesium phenates, magnesium sulfonates, magnesium salicylates, metal carbonates, related components including borated detergents, and any combination thereof. The detergents can be neutral, mildly overbased, or highly overbased. The amount of detergents usually contributes a total base number (TBN) in a range from 1 to 9 for the formulated lubricant composition. Metal detergents have been chosen from alkali or alkaline earth calcium or magnesium phenates, sulfonates, salicylates, carbonates and similar components.

Antioxidants have been chosen from hindered phenols, arylamines, dihydroquinolines, phosphates, thiol/thiolester/disulfide/trisulfide, low sulfur peroxide decomposers and other related components. These additives are rich in sulfur, phosphorus and/or ash content as they form strong chemical films to the metal surfaces and thus need to be used in limited amount in reduced sulfur, ash and phosphorous lubricating oils.

Inhibitors and antirust additives may be used as needed. Seal swell control components and defoamants may be used with the mixtures of this invention. Various friction modifiers may also be utilized. Examples include but are not limited to amines, alcohols, esters, diols, triols, polyols, fatty amides, various molybdenum phosphorodithioates (MoDTP), molybdenum dithiocarbamates (MoDTC), sulfur/phosphorus free organic molybdenum components, molybdenum trinuclear components, and any combination thereof.

In a preferred embodiment, this new synergistic combination has significantly improved these critical performance parameters while maintaining excellent compatibility to exhaust after-treatment devices. This embodiment comprises a novel anti-wear, friction reduction and antioxidant system consisting of organic borates, non-corrosive sulfur additives, high level of ashless antioxidants and low levels of zinc dithiophosphates. More specifically, this formulated engine oil embodiment comprises about 100 to 630 ppm phosphorus, and about 0.1 to 0.3 wt % sulfur and from about 80 to 450 ppm boron, and about 0.5 to 3.0 wt % ashless antioxidants such as total amounts of hindered phenols and arylamines.

These components can be used with a variety of base stocks, including group I, II, III, IV, and V, and gas-to-liquids (“GTL”) as well as a variety of mixtures thereof. However, due to other performance requirements including volatility, stability, viscometrics, and cleanliness feature, premium engine oils prefer to use group II and higher (“Group II+”) base oils to ensure that they can achieve desirable overall performance levels as well as maximizing the full potential of the unique synergies among additives. Additional significant synergies were identified among alkylated aromatics and Group II+high performance base stocks including Group II, III, IV, V, VI or GTL base stocks.

Groups I, II, III, IV and V are broad categories of base oil stocks developed and defined by the American Petroleum Institute (API Publication 1509; www.API.org) to create guidelines for lubricant base oils. Group I base stocks generally have a viscosity index of between about 80 to 120 and contain greater than about 0.03% sulfur and/or less than about 90% saturates. Group II base stocks generally have a viscosity index of between about 80 to 120, and contain less than or equal to about 0.03% sulfur and greater than or equal to about 90% saturates. Group III stock generally has a viscosity index greater than about 120 and contains less than or equal to about 0.03% sulfur and greater than about 90% saturates. Group IV includes polyalphaolefins (PAO). Group V base stocks include base stocks not included in Groups I-IV. Table 1 summarizes properties of each of these five groups.

TABLE 1 Base Stock Properties Saturates Sulfur Viscosity Index Group I <90% and/or >0.03% and ≧80 and < 120 Group II ≧90% and ≦0.03% and ≧80 and < 120 Group III ≧90% and ≦0.03% and ≧120 Group IV Polyalphaolefins (PAO) Group V All other base oil stocks not included in Groups I, II, III, or IV

Base stocks having a high paraffinic/naphthenic and saturation nature of greater than 90 weight percent can often be used advantageously in certain embodiments. Such base stocks include Group II and/or Group III hydroprocessed or hydrocracked base stocks, or their synthetic counterparts such as polyalphaolefin oils, GTL or similar base oils or mixtures of similar base oils.

In a preferred embodiment, at least about 20 percent of the total composition should consist of such Group II or Group III base stocks or GTL, with at least about 30 percent being preferable, and more than about 80 percent on being most preferable. Gas to liquid base stocks can also be preferentially used with the components of this invention as a portion or all of the base stocks used to formulate the finished lubricant. We have discovered, favorable improvement when the components of this invention are added to lubricating systems comprising primarily Group II, Group III and/or GTL base stocks compared to lesser quantities of alternate fluids.

GTL materials are materials that are derived via one or more synthesis, combination, transformation, rearrangement, and/or degradation/deconstructive processes from gaseous carbon-containing compounds, hydrogen-containing compounds, and/or elements as feedstocks such as hydrogen, carbon dioxide, carbon monoxide, water, methane, ethane, ethylene, acetylene, propane, propylene, propyne, butane, butylenes, and butynes. GTL base stocks and base oils are GTL materials of lubricating viscosity that are generally derived from hydrocarbons, for example waxy synthesized hydrocarbons, that are themselves derived from simpler gaseous carbon-containing compounds, hydrogen-containing compounds and/or elements as feedstocks. GTL base stock(s) include oils boiling in the lube oil boiling range separated/fractionated from GTL materials such as by, for example, distillation or thermal diffusion, and subsequently subjected to well-known catalytic or solvent dewaxing processes to produce lube oils of reduced/low pour point; wax isomerates, comprising, for example, hydroisomerized or isodewaxed synthesized hydrocarbons; hydroisomerized or isodewaxed Fischer-Tropsch (“F-T”) material (i.e., hydrocarbons, waxy hydrocarbons, waxes and possible analogous oxygenates); preferably hydroisomerized or isodewaxed F-T hydrocarbons or hydroisomerized or isodewaxed F-T waxes, hydroisomerized or isodewaxed synthesized waxes, or mixtures thereof.

GTL base stock(s) derived from GTL materials, especially, hydroisomerized/isodewaxed F-T material derived base stock(s), and other hydroisomerized/isodewaxed wax derived base stock(s) are characterized typically as having kinematic viscosities at 100° C. of from about 2 mm2/s to about 50 mm2/s, preferably from about 3 mm2/s to about 50 mm2/s, more preferably from about 3.5 mm2/s to about 30 mm2/s, as exemplified by a GTL base stock derived by the isodewaxing of F-T wax, which has a kinematic viscosity of about 4 mm2/s at 100° C. and a viscosity index of about 130 or greater. The term GTL base oil/base stock and/or wax isomerate base oil/base stock as used herein and in the claims is to be understood as embracing individual fractions of GTL base stock/base oil or wax isomerate base stock/base oil as recovered in the production process, mixtures of two or more GTL base stocks/base oil fractions and/or wax isomerate base stocks/base oil fractions, as well as mixtures of one or two or more low viscosity GTL base stock(s)/base oil fraction(s) and/or wax isomerate base stock(s)/base oil fraction(s) with one, two or more high viscosity GTL base stock(s)/base oil fraction(s) and/or wax isomerate base stock(s)/base oil fraction(s) to produce a dumbbell blend wherein the blend exhibits a viscosity within the aforesaid recited range. Reference herein to Kinematic viscosity refers to a measurement made by ASTM method D445.

GTL base stocks and base oils derived from GTL materials, especially hydroisomerized/isodewaxed F-T material derived base stock(s), and other hydroisomerized/isodewaxed wax-derived base stock(s), such as wax hydroisomerates/isodewaxates, which can be used as base stock components of this invention are further characterized typically as having pour points of about −5° C. or lower, preferably about −10° C. or lower, more preferably about −15° C. or lower, still more preferably about −20° C. or lower, and under some conditions may have advantageous pour points of about −25° C. or lower, with useful pour points of about −30° C. to about −40° C. or lower. If necessary, a separate dewaxing step may be practiced to achieve the desired pour point. References herein to pour point refer to measurement made by ASTM D97 and similar automated versions.

The GTL base stock(s) derived from GTL materials, especially hydroisomerized/isodewaxed F-T material derived base stock(s), and other hydroisomerized/isodewaxed wax-derived base stock(s) which are base stock components which can be used in this invention are also characterized typically as having viscosity indices of 80 or greater, preferably 100 or greater, and more preferably 120 or greater. Additionally, in certain particular instances, viscosity index of these base stocks may be preferably 130 or greater, more preferably 135 or greater, and even more preferably 140 or greater. For example, GTL base stock(s) that derive from GTL materials preferably F-T materials especially F-T wax generally have a viscosity index of 130 or greater. References herein to viscosity index refer to ASTM method D2270.

In addition, the GTL base stock(s) are typically highly paraffinic of greater than 90 percent saturates), and may contain mixtures of monocycloparaffins and multicycloparaffins in combination with non-cyclic isoparaffins. The ratio of the naphthenic (i.e., cycloparaffin) content in such combinations varies with the catalyst and temperature used. Further, GTL base stocks and base oils typically have very low sulfur and nitrogen content, generally containing less than about 10 ppm, and more typically less than about 5 ppm of each of these elements. The sulfur and nitrogen content of GTL base stock and base oil obtained by the hydroisomerization/isodewaxing of F-T material, especially F-T wax is essentially nil.

In a preferred embodiment, the GTL base stock(s) comprises paraffinic materials that consist predominantly of non-cyclic isoparaffins and only minor amounts of cycloparaffins. These GTL base stock(s) typically comprise paraffinic materials that consist of greater than 60 wt % non-cyclic isoparaffins, preferably greater than 80 wt % non-cyclic isoparaffins, more preferably greater than 85 wt % non-cyclic isoparaffins, and most preferably greater than 90 wt % non-cyclic isoparaffins.

Useful compositions of GTL base stock(s), hydroisomerized or isodewaxed F-T material derived base stock(s), and wax-derived hydroisomerized/isodewaxed base stock(s), such as wax isomerates/isodewaxates, are recited in U.S. Pat. Nos. 6,080,301; 6,090,989, and 6,165,949 for example.

The principle advantage of one embodiment of this invention is the unique synergistic combination of organic borates, non-corrosive sulfur additives in the presence of low level zinc dithiophosphates and high level of ashless antioxidants that provides favorable oxidation, corrosion stability, and more importantly, anti-wear performance. These favorable performance levels can be achieved while reducing the levels of sulfur, phosphorus and zinc in the engine oil formulations compared to the typical engine oil used today.

In one embodiment, the general formulation of the low SAP engine oil is summarized in Table 2. In this table and throughout the application weight percent is intended to be active ingredient weight percent of the entire composition unless otherwise stated.

TABLE 2 Elements in Formulated Oils Component Type Wt % (ppm) + Other Restrictions Organic-containing 0.1-8.0% 80 to 450 PPM boron boron additive Zinc dithiophosphate 0.2-2.0% 100 to 530 PPM phosophorous and additive 105 to 710 PPM zinc Dispersant-detergent-  <15.0% inhibitor system Non-corrosive ashless 0.1-4.0% 1,000 to 3,000 PPM sulfur sulfur additive Ashless antioxidants 0.5-3.0%

EXAMPLES

Table 3 illustrates low temperature stabilities for different ashless antiwear additives for low phosphorous lubricant oils with a phosphorous level of 0.05 weight percent of the composition. Table 3 illustrates various embodiments for two reference base oils formulations. Both base Reference oils A and B are formulated with the premium Group III base oils.

TABLE 3 Entry 7 1 2 3 4 5 6 Comparative oil Reference Comparative Comparative Comparative Comparative Reference 5 oil A oil 1 oil 2 oil 3 oil 4 oil B RN 4717 Ashless AW 0.2% Ald-4 0.3% Ald-4 0.2% Ald-2 0.3% Ald-2 .25% Dibenzyl additive S2-pyridine S2-pyridine S2-pyridine S2-pyridine Disulfide 0.05% P 0.05% P 0.05% P 0.05% P 0.05% P (0.05% P) (0.05% P) Solubility C & B Dropout Dropout C & B C & B C & B C & B Appearance at 5C At 5C Cu 3 1A 1A Corrosion hrs/250° F. (D130-6) Cu 3 2C 1B 1B 2B 2C 1B 1B Corrosion hrs/210° F./ (D130-8) H2O Cu 24 1A 2A 2A 3A 4A 1A 4A Corrosion hrs/250° F. (D130-9) PDSC Onset T 246.7 239.6 245 242.7 238.8 229.7 228.5 (Ramp (° C.) 10° C./min) 288° C., 16 hrs Tube Rating 3 6 6.9 4.5 5.5 3.8 3.3 (1 = Clean) 4 Ball Wear WSD 0.6 0.6 (D4172) (mm) 40 Kg/1800 K Factor 7 6.2 rpm/30 min./ 200° F. Aldrithiol-4 4,4′- Disulfide [2645-22-9] dipyridyl 4 Ball EP LNS (Kg) Aldrithiol-2 2,2′- Disulfide [2127-03-9] 80 80 (D2783) dipyridyl 30° C./10 Weld Ld 200 200 sec./1760 rpm (Kg) LWI 34.5 35.2 HFRR Ave. 0.147 0.107 Friction 0.7 Kg/60 % Ave. 12.3 10.7 Hz/0.5 mm/ film 60 min./75° Scar X/Y 0.3/0.77 0.30/0.73 C. (mm) Calc. Sc. 0.181 0.173 Area

Now referring to Table 3, comparative oils 1, 2, 3 and 4 are variations of reference oil A. The formulation for reference oil A is disclosed in Table 4.

TABLE 4 Low ash Descriptions engine oil Blend Code 4866XNP005-D Batch Number 1 Additive Sytem 1 Antioxidants 2 Additive System 2 Detergents/ 9.25 dispersants Additive System 3 Viscosity modifiers 14 Additive System 4 Other performance 0.3 additives Base oil System Group III Balance BASELINE D 130 8 Corrosion of Cu by 2C Petroleum D 130 9 250 F./24 Corrosion of Cu by 1A hrs Petroleum D445 5 KV at 100 Kinematic Viscosity 9.868 C., CST @100 C. D5293 6 AppVis App. Viscosity 4400 CCS -30, CP @ Low Temp D6443 MAGNESIUM, Add Metals in Lubes 0.0469 WT % D6443 SULFUR, Add Metals in Lubes 0.1825 WT % D6443 PHOSPHORUS, Add Metals in Lubes 0.0476 WT % D6443 CALCIUM, Add Metals in Lubes 0.0329 WT % D6443 CHLORINE, Add Metals in Lubes 0.0095 WT % D6443 COPPER, Add Metals in Lubes <0.0020000001 WT % D6443 ZINC, Add Metals in Lubes 0.0554 WT %

Again referring to table 3, comparative oil 5 is a variations of reference oil B. The formulation for reference oil B is disclosed in Table 5.

TABLE 5 Blend Code OSCARLOWSPA-C Batch Number ZnDTP tree base blend 1 Base oil System Group III Base Oi) Balance Additive System 1 Antioxidants 1.5 Additive System 2 Dispersants/Detergents 9.5 Additive System 3 Viscosity Modifiers 7 Additive System 4 All other performance additives 0..05 Group III Base Oil with a minimum VI of 120, a typical pour point of - 15C and a typical sul- REFERENCE fur <10 ppm D 445 5 KV at 100 C., CST Kinematic Viscosity at 100 C. 12.1 D 874 Sulfated Ash, WT % Sulfated Ash from Lubes, Addtv 0.32 D2896 TBN of Petroleum Products 4.12 D4683, CP HTHS Tapered Bearing Visc Test 3.53 D4684 6 Yield Stress, PA Yield Stress, App. Viscosity >350 D4684 6 Appar Viscos 1, CP Yield Stress, App. Viscosity >500000 D4684 6 Appar Viscos 2, CP Yield Stress, App. Viscosity >500000 D4684 6 Appar Viscos 3, CP Yield Stress, App. Viscosity >500000 D5293 6 AppVis CCS −30, CP App. Viscosity @ Low Temp 5080 D6443 MAGNESIUM, WT % Add Metals in Lubes 0.0494 D6443 SULFUR, WT % Add Metals in Lubes 0.072 D6443 PHOSPHORUS, WT % Add Metals in Lubes <0.0020000001 D6443 CALCIUM, WT % Add Metals in Lubes 0.0334 D6443 CHLORINE, WT % Add Metals in Lubes 0.0047 D6443 COPPER, WT % Add Metals in Lubes <0.0020000001 D6443 ZINC, WT % Add Metals in Lubes <0.0020000001 D5185 Boron, PPM 170 D5185 Molybdenum, PPM <0.5

Table 3 also illustrates copper corrosion test from the ASTM D-130 method. Table 6 illustrates the various classifications from the ASTDM Copper Corrosion test. As shown in table 6, Classifications 1A, 1B, 2A, and 2B are the non-corrosive preferred classifications with classifications 2C, 2D, 2,E, 3A, 3B, 4A, 4B, and 4C being the non preferred classifications.

TABLE 6 ASTM D-130 Copper Corrosion Tests Classifi- Corrosion cation Designation Description Comment Freshly — — Non-corrosive, polished preferred strip 1A Slightly tarnish Light orange, Non-corrosive, almost the same preferred as freshly pol. Strip 1B Slightly tarnish Dark orange Non-corrosive, preferred 2A Moderate tarnish Claret red Non-corrosive, preferred 2B Moderate tarnish Lavender Non-corrosive, preferred 2C Moderate tarnish Multicolored with Not preferred lavender blue or silver 2D Moderate tarnish Silvery Not preferred 2E Moderate tarnish Brassy or gold Not preferred 3A Dark tarnish Magenta overcast Not preferred on brassy strip 3B Dark tarnish Multicolored with Not preferred red and green, but no gray 4A Corrosion Transparent black, Not preferred dark gray or brown with green 4B Corrosion Green barely showing Not preferred 4C Corrosion Graphite or luster- Not preferred less black glassy or jet black

As shown in columns 2 and 3 of table 3, very poor low temperature stability, labeled as solubility appearance is observed when 0.2 to 0.3% of Aldrithiol-4 was respectively added to the low phosphorous reference A base oil formulation in column 1. This poor oil compatibility issue correlates well with the poor hot tube deposit test results. As shown in columns 4 and 5 adding 0.2 and 0.3% of Aldrithiol-2 improves the oil compatibility but the copper corrosion becomes unacceptable in columns 4 and 5.

A similar evaluation was conducted when 0.25% dibenzyl disulfide described in comparative oil 5 is added to reference oil B base formulation as described in table 3. In this example, the 4-Ball wear and EP performance improves slightly, and the average friction and calculated wear scar area in High Frequency Reciprocating Rig (HFRR) reduces significantly comparing reference oil B with comparative oil 5. However, the copper corrosion at 250° F. for the 24 hour test conditions remains poor as shown by a 4A rating for comparative oil 5.

Now referring to table 6, any ratings in classification categories 2C-2E, 3 and 4 are not preferred as they can cause darkening and discoloration of the copper coupons that strongly indicate corrosive or near corrosive behavior. To achieve the additive synergy embodiment described in this invention, a very stringent preferred range is established for defining non-corrosive sulfur additives. Accordingly, dibenzyl disulfide and Aldrithiol-2 are not preferred due to their corrosive sulfur species and thus not recommended for low SAP engine oils.

Reference oil B is a ZnDTP free blend developed so different amounts of ZnDTP as well as other non-corrosive organic sulfur additives can be added to show comparative performance results. The base formulation is formulated with Group III base oils with a minimum of 120 viscosity index, a typical pour point of −15° C., a typical Noack of 15 and a typical sulfur of 10 ppm with a miximum sulfur content less than 30 ppm. Similarly, the base engine oil formulated is also formulated with GTL oils with a minimum of 135 viscosity index, a typical pour point of −17° C. and a typical sulfur of less than 1 ppm.

Table 7, illustrates that very good oxidation/corrosion control can be achieved with combinations of non-corrosive sulfur additives, borated dispersants, high level of ashless antioxidants and low level of zinc dithiophosphates in a low Phosphorus engine oil. Columns one and two represent reference oils C and D and Columns 3, 4 and 5 represent respectively comparative oils 6, 7, and 8 which are variation of reference oil D. Reference oil C is a low SAP group III base oil with 0.1 weight percent phosphorous. Whereas, reference oil D and example comparative oils 6, 7, and 8 are Group III low SAP base oils with 0.05 weight percent phosphorous. Slight variations in the formulations are also documented in Table 7.

TABLE 7 Entry 3 4 5 1 2 Comparative Comparative Comparative Reference Reference oil 6 oil 7 oil 8 oil C oil D Ashless DTC Sulfur ester DTC/Sulfur ZnDTP 1% 0.50% 0.50% 0.50% 0.50% Ashless AW additive .25% VL981 .5% RC-2411 .25% VL981 Ashless AW additive .25% RC-2515 Borated Dispersant and 9.5% 9.5% 9.5% 9.5% 9.5% Ashless Antioxidant Low ash/S/P Gp III Estimate by (0.10% P) (0.05% P) (0.05% P) (0.05% P) (0.05% P) theory Solubility Clear and Clear and Clear and Clear and Clear and Appearance bright bright bright bright bright 4 Ball Wear (D4172) WSD (mm) 0.59 0.62 0.57 0.57 0.53 40 Kg/1800 rpm/.5 hr/200 F. K Factor 5.7 7.0 5.0 4.8 3.7 4 Ball EP (D2783) LNS (Kg) 80 80 80 100 100 30° C./10 sec./1760 rpm Weld Ld (Kg) 200 200 200 200 200 LWI 35.1 34.5 41.5 41.5 41.8 Cu Corrosion (D130-6) 3 hrs/250 F. 1A 1A 1A 1A 1A Cu Corrosion (D130-8) 3 hrs/210 F./H2O 1A 1B 1B 1B 1A Cu Corrosion (D130-9) 24 hrs/250 F. 1A 1A 1B 1B 1B PDSC (Ramp 10° C./min) Onset T (° C.) 232 229.7 233.6 237.6 237.7 Hot Tube Test 3.5 3.8 3 2.8 3.3 (288 C./16 hr) HFRR Ave. Friction 0.139 0.147 0.118 0.105 0.121 0.7 Kg/60 Hz/0.5 mm/ Calc. Sc. Area 0.174 0.181 0.173 0.173 0.154 60 min./75° C. TBN D2896 4.27 4.23 4.14 4.04 4.23 Sulfated Ash (wt %) D874 0.53 0.38 0.38 0.32 0.38 Boron (wt %) D5185 0.017 0.017 0.017 0.017 0.017 Phosphorus (wt %) D6443 0.1003 0.0507 0.0488 0.0482 0.0494 Zinc (wt %) D6443 0.1118 0.0577 0.0573 0.0564 0.0569 Calcium (wt %) D6443 0.0329 0.0332 0.0331 0.0328 0.0327 Magnesium (wt %) D6443 0.0595 0.0496 0.0507 0.0505 0.0479 Copper (wt %) D6443 <0.002 <0.002 <0.002 <0.002 <0.002 Chlorine (wt %) D6443 0.0047 0.0049 0.0052 0.0053 0.0049 Sulfur (wt %) D6443 0.2799 0.1783 0.2109 0.2198 0.2526 Pin-on-V Block Pass Pass Pass 500 Lb, 210 minutes Ave Scar (mm) 0.432 0.418 0.387

The non-corrosive sulfur additives in comparative example embodiment oil 6 is an ashless dithiocarbamates (“DTC”) called Vanlube™981. Vanlube™981 is an experimental additive available from R.T. Vanderbilt Chemical Company. Comparative oils 7 and 8 are specific sulfurized ester/olefins with low sulfur content with or without DTC as in comparative oils 7 and 8 and are respectively labeled RC-2411 and RC-2515. RC-2411 and RC-2515 are commercially available from Rhein Chemie Chemical Company] The good corrosion control is evidenced by 1A to 2B copper corrosion ratings under various conditions. The anti-oxidation performance of oils 6, 7, and 8 are slightly better than reference oil D. These properties are evidenced by Pressurized Differential Scanning Calorimetry (“PDSC”) by about 4 to 8 degrees higher onset temperature. In the ramping method of PDSC of 10 degrees Celsius per minute, the higher the onset temperature, the better the resistance to oxidation. Generally, oxidation rates generally double with about 10 degrees Celsius increase in temperature. Therefore, these results can be translated into about 40 percent to 80 percent better in terms of control of viscosity or acid number increases or any other comparable measurements for control of oxidation.

When non-corrosive sulfur additives were added as in comparative embodiment oils 6, 7 and 8, the 4-Ball wear and 4-Ball EP results are all consistently better than the Reference oil D. A slight reduction in wear scar diameter of between 8 to 14 percent can be observed for the ASTDM D4172 4-Ball wear conditions which translate into a 29 to 47 percent calculated reduction in wear volume shown as the K-factor. The last non-seizure load (“LNS”) and load-wear index (“LWI”) are 21 to 25 percent better for oils 6, 7, and 8 when compared to the performance of reference 4 in the 4-Ball EP tests.

The HFRR data showed that those non-corrosive sulfur additives can help maintain excellent frictional properties as well as wear reduction as evidenced by the lower average coefficients of friction of between 18 to 29 and approximately 4 to 15 percent smaller calculated scar area. Overall, example comparison oils 6, 7, and 8 formulated with 0.05% phosphorus plus non-corrosive sulfur additives provide favorable performance when compared to a typical engine oil, with full load of ZDDP as in the 1 weight percent reference oil C. This demonstrates the strong synergistic effect exists of the various embodiments of example oils 6, 7, and 8. All the additive components of examples 6, 7, and 8 are fully compatible with engine oils as evidenced by their clear and bright appearance in storage over a period of several months. Table 7 demonstrates satisfactory stability for oils containing non-corrosive sulfur additives. Lastly, the pin-on-. V block shown as Falex wear test results correlate well with 4-Ball wear/EP results indicating better wear control with comparative oils 6 and 7 versus Reference oil D.

In Table 8, another low SAP oil was also evaluated. Comparative oil 9 is a low SAP Group III base with a final composition of 0.025 weight percent phosphorous.

TABLE 8 Entry 4 1 2 3 Comparative oil 9 Base Reference E Reference F DTC/S ester ZnDTP Secondary ZDDP 0% 0.25% 0.50% 0.25% Ashless AW additive .25% VL981 .25% RC-2411 Borated Dispersant and 9.5% 9.5% 9.5% 9.5% Ashless Antioxidant Low ash/S/P Gp III (0% P) (0.025% P) (0.05% P) (0.025% P) Solubility C & B C & B C & B C & B Appearance 4 Ball EP (D2783) LNS (Kg) 50 63 80 80 30 C./10 sec./1760 rpm Weld Ld (Kg) 160 200 200 200 LWI 22.0 28.21 34.5 34.4 Cu Corrosion (D130-6) 3 hrs/250° F. 1B 1B 1A 1B Cu Corrosion (D130-8) 3 hrs/210° F./H2O 3A 1A 1B 1B HFRR Ave. Friction 0.144 0.127 0.147 0.126 0.7 Kg/60 Hz/0.5 mm/ Calc. Sc. Area 0.211 0.173 0.181 0.173 60 min./75° C. TBN D2896 4.12 5.45 4.23 4.52 Sulfated Ash (wt %) D874 0.32 0.33 0.38 0.33 Boron (wt %) D5185 0.017 0.017 0.017 0.017 Phosphorus (wt %) D6443 <0.002 0.0244 0.0507 0.0258 Zinc (wt %) D6443 <0.002 0.0287 0.0577 0.03 Calcium (wt %) D6443 0.4859 0.0331 0.0332 0.0323 Magnesium (wt %) D6443 0.0034 0.0501 0.0496 0.0508 Copper (wt %) D6443 <0.002 <0.002 <0.002 <0.002 Chlorine (wt %) D6443 0.0055 0.0048 0.0049 0.0049 Sulfur (wt %) D6443 0.072 0.124 0.1783 0.1849

Equivalent average friction coefficients and calculated wear scar area were observed in HFRR tests, but much improved last non-seizure (LNS) load and load-wear index (LWI) were found in 4-Ball EP test when comparative oil 9 is compared to Reference oil E. Actually, the 4-Ball EP performance of comparative oil D is almost equivalent to that of Reference F where twice the amount of ZDDP is used as shown by a final phosphorus weight percent of 0.05. Although Reference oil E has strong 4-Ball EP performance, the HFRR data are not as good as comparative oil 9 and Reference oil E. This data clearly indicates that too much ZDDP can be antagonistic to the frictional property. The base formulation, shown as base in column of 1 of table 8 was also used to blend oils in Tables 6 and 7 and is fully described in Table 5 for reference.

Table 9 illustrates the evaluation of non-corrosive sulfur additives in low SAP commercial vehicle lubricants (“CVL”). Table 9 is formulated with a low SAP base oil with no phosphorous.

TABLE 9 Entry 2 3 4 1 Comparative Comparative Comparative oil Reference oil 10 oil 11 12 Commercial Engine Oil Oil G Ashless DTC Borated GMO DTC + B-GMO ZnDTP Secondary 0.30% 0.30% 0.30% 0.30% ZDDP Ashless Antiwear 0.3% VL 981 0.3% VL 981 Ashless Friction Modifier 0.5% B-GMO 0.5% B-GMO Borated Dispersants and 9.71% 9.71% 9.71% 9.71% Antioxidants Low ash/S/P (0.03% P) (0.03% P) (0.03% P) (0.03% P) Solubility C&B C&B C&B C&B Appearance 4 Ball Wear WSD (mm) 0.61 0.52 0.48 0.47 40 Kg/1200 rpm/60 min./200° K Factor 4.86 2.36 1.71 1.44 F. 4 Ball Wear WSD (mm) 0.41 0.40 0.33 0.40 40 Kg/600 rpm/30 min./200° F. K Factor 2.67 2.46 0.57 2.46 4 Ball EP (D2783) LNS (Kg) 80 100 80 80 30 C./10 sec./1760 rpm Weld Ld (Kg) 200 200 200 200 LWI 33.6 41.2 34.0 34.2 Cu Corrosion (D130-6) 3 hrs/250° F. 1A 1A 1A 1B Cu Corrosion (D130-8) 3 hrs/210° F./H2O 1A 1A 1A 1A Cu Corrosion (D130-9) 24 hrs/250° F. 1B 1B 1B 1B TBN D2896 7.88 8.04 8 7.98 Sulfated Ash (wt %) D874 0.76 0.79 0.77 0.77 Phosphorus (wt %) D6443 0.0286 0.0287 0.0291 0.0285 Zinc (wt %) 0.0324 0.0326 0.0332 0.0325 Calcium (wt %) 0.1983 0.1986 0.1983 0.1967 Magnesium (wt %) 0.0038 0.0025 0.0024 0.0024 Copper (wt %) <0.002 <0.002 <0.002 <0.002 Chlorine (wt %) 0.008 0.008 0.0076 0.0077 Sulfur (wt %) 0.2237 0.2663 0.2233 0.2645

The composition of the base formulation of Table 9 is listed in Table 10. As shown in Table 10 and column 3 of Table 9, this base oil has no phosphorous. The base oil system consists of about 50% Group III and roughly about 20% Group I base oils. All oils containing ZDDP and other sulfur/boron additives in Table 9 and 11 are formulated from the base formulation. Similarly, another base formulation is formulated with GTL base oils. The base oil system consists of more than 50% GTL and less than 20% Group I base oils.

TABLE 10 Commercial Descriptions engine oil Blend Code LSAP01-A Batch Number ZnDTP free base blend 1 Base oil system Mixed Group I & III base oils Balanced Additive system 1 Antioxidants 0.5 Additive system 2 Detergent/dispersants 17.8 Additive system 3 Viscosity modifiers 9 Additive system 4 Other performance additives 1.2

Now referring to table 9, in example oil 10, a 0.3 weight percent of a non-corrosive sulfur additive, in this example an ashless dithiocarbamate, is included in the engine oil formulated with 0.03 weight percent phosphorus as shown by reference oil G. The 4-Ball wear performance resulted in 2 to 15 percent improvement in wear reduction or wear scar diameter (“WSD”) and 8 to 51 percent improvement in calculated wear volume or K-factor. Comparative oils 11 and 12 illustrate the synergists effect of combining borated GMO with borated dispersants.

Similarly, Table 11 illustrates the 4-Ball EP and Hot Tube performance of the combination of 0.3 percent ZDDP and 0.3 percent of a non-corrosive sulfur additive for comparative oil 13 versus the 0.6 percent ZDDP reference oil H. The total AW/EP additive treat rate is the same 0.6 percent and the EP performance is about the same, but the Hot Tube of Entry 4 is much better indicating a cleaner environment. The 4-Ball EP performance of comparative oil 13 is stronger than reference oil I with reduced ZDDP at 0.3% and the base oil in column 3 with 0% ZDDP.

TABLE 11 Entry 4 1 2 Comparative Reference Reference 3 oil 13 Commercial Engine Oil oil H oil I Base Ashless DTC ZnDTP 0.60% 0.30% 0% 0.30% Ashless Antiwear 0.3% VL 981 Ashless Friction Modifier Borated Dispersants 9.71% 9.71% 9.71% 9.71% Antioxidants Low ash/S/P (0.06% P) (0.03% P) 0% P (0.03% P) Solubility C&B C&B C&B C&B Appearance 4 Ball EP (D2783) LNS (Kg) 100 80 63 100 30 C./10 sec./1760 rpm Weld Ld (Kg) 200 200 160 200 LWI 41.5 33.6 26.5 41.2 Cu Corrosion (D130-6) 3 hrs/250 F. 1A 1A 1B 1A Cu Corrosion (D130-8) 3 hrs/210 F./H2O 1A 1A 1B 1A Cu Corrosion (D130-9) 24 hrs/250 F. 1A 1B 2A 1B Hot Tube Test 4.0 1.5 (305 C./16 hr)

In summary, a new low SAP engine oil system has been discovered based on very unique combinations of non-corrosive sulfur additives, low level of ZDDP, borated components, with preferably high level of ashless anti-oxidants. This formulation exhibits outstanding and unexpected performance to modern engines. One embodiment of this discovery provides an effective way to reduce the amount of ZDDP for contemporary engine oils while maintaining excellent wear, oxidation and corrosion protection. This unique component synergism concept is believed to be applicable to similar formulations containing low sulfur base oils of less than 300 ppm, borated additives with borated hydroxyesters such as borated GMO, and alternate organic borates such as borated dispersants, non-corrosive sulfur additives, and preferably with ashless antioxidants.

Claims

1. A composition, comprising:

a. a lubricating oil basestock;
b. an organic boron containing additive present in an amount of at least 0.01 and less than 8.0 weight percent of the composition;
c. a dispersant-detergent-inhibitor system of less than 15 weight percent of the composition;
d. a non-corrosive ashless sulfur additive present in an amount of at least 0.1 and less than 4.0 weight percent of the composition;
e. a zinc dithiophosphate additive present in an amount of at least 0.2 weight percent of the composition and less than 2.0 weight percent of the composition; and
f. the composition having at least 100 PPM and less than 630 PPM phosphorus, at least 105 PPM and less than 710 PPM zinc, at least 1,000 PPM and less than 3,000 PPM sulfur, at least 80 PPM and less than 450 PPM Boron.

2. The composition of claim 1 further comprising at least one performance additive wherein the additives are chosen form the group comprising zinc dithiophosphates, borated or non-borated dispersants, phenolic and aminic ashless anti-oxidants, metal detergents, molybdenum or organic friction modifiers, defoamants, seal swell additives, pour point depressants and others including contemporary dispersant-detergent-inhibitor (DDI) additive packages, and any combination thereof.

3. The composition of claim 1 wherein the base stock is chosen from the group consisting of group II base stocks, group III base stocks, group IV base stocks, and group V base stocks, gas-to-liquids base stocks, and any combination thereof.

4. The composition of claim 1 wherein the dispersant systems comprises additives chosen from the group consisting of borated and non-borated succinimides, succinic acid-esters and amides, alkylphenol-polyamine coupled Mannich adducts, and any combination thereof.

5. The composition of claim 1 further comprising an ashless antioxidant additive.

6. The composition of claim 1 further comprising a metallic detergent or detergent system.

7. The composition of claim 6 wherein the detergent system provides a total base number (TBN) less than 9, preferably less than 7 and most preferably less than 5, to the formulated lubricant composition.

8. The composition of claim 1 further comprising a viscosity modifier additive.

9. The composition of claim 1 wherein the organic borate is a borated hydroxyl esters chosen from the group consisting of borated glycerol mono-oleate, borated glycerol di-oleate, borated glycerol tri-oleate, borated glycerol mono-cocoate, borated mono-talloate, borated glycerol mono-sorbitate, borated polyol esters and any combination thereof

10. The composition of claim 1 wherein the non corrosive sulfur additive is chosen from the group consisting of ashless derivatives of thiadiazoles, ashless derivatives of benzothiazoles, ashless alkyl, aryl sulfides/di-sulfides/tri-sulfide including thianthrene, diphenyl disulfide, dinonyl disulfide, dipyridyl disulfide, and their alkylates, ashless dithiocarbamates, thioesters/sulfurized esters, thioglycolates, dialkyl thiodipropionates, dialkyl dithiopropionates, and any combination thereof.

11. The composition of claim 10 wherein the non-corrosive, organic sulfur additive is a sulfur/nitrogen containing, heterocyclic or non-heterocyclic antiwear-antioxidant additive.

12. The composition of claim 11 wherein the non-corrosive, organic sulfur additive is an ashless dithiocarbamate additive.

13. The composition of claim 11 wherein the non-corrosive, organic sulfur additive is thiadiazole-derived antiwear additive.

14. A lubricant additive system for a lubricant composition, comprising:

a. an organic boron containing additive of at least 0.4 weight percent and less than 32 weight percent of the additive;
b. a detergent-dispersant system of less than 60 percent weight percent of the additive;
c. a zinc dithiophosphate additive of at least 0.8 weight percent of the composition and less than 8.0 weight percent of the additive; and
d. a non-corrosive ashless sulfur additive of at least 0.4 and less than 16.0 weight percent of the additive.

15. The lubricant additive of claim 14 wherein the total lubricant additive treat is in the range of at least 0.1 weight percent to 25 weight percent of the lubricant composition.

16. The lubricant additive of claim 14 further comprising a molybdenum additive.

17. The lubricant additive of claim 16 wherein the molybdenum additive is an organic molybdenum additive.

18. The lubricant additive of claim 14 wherein the zinc dithiophosphate additive comprises a primary alkyl alcohol derived, or a secondary alkyl alcohol derived zinc dithiophosphate or a combination thereof.

19. A method comprising

a. obtaining a composition comprising a lubricating oil basestock, an organic boron containing additive present in the amount of at least 0.1 and less than 8 weight percent of the composition, a dispersant-detergent-inhibitor system of less than 15 percent weight percent of the composition, a zinc dithiophosphate additive present in the amount of at least 0.2 weight percent of the composition and less than 2.0, weight percent of the composition, a non corrosive ashless sulfur additive present in the amount of at least 0.1 and less than 4.0 weight percent of the composition wherein the composition has at least 100 PPM and less than 630 PPM phosphorus, at least 105 PPM and less than 710 PPM zinc, at least 1,000 PPM and less than 30,000 PPM sulfur, at least 80 PPM and less than 450 PPM Boron; and
b. lubricating an engine with the composition to achieve favorable anti-wear, oxidation and cleanliness.

20. A method for reducing sulfur in exhaust gasses in an internal combustion engine, comprising:

a. obtaining a composition comprising a lubricating oil basestock, an organic boron containing additive present in the amount of at least 0.1 and less than 8 weight percent of the composition, a dispersant-detergent-inhibitor system of less than 15 percent weight percent of the composition, zinc dithiophosphate additive present in the amount of at least 0.2 weight percent of the composition and less than 2.0, weight percent of the composition, a non corrosive ashless sulfur additive present in the amount of at least 0.1 and less than 4.0 weight percent of the composition wherein the composition has at least 100 PPM and less than 630 PPM phosphorus, at least 105 PPM and less than 710 PPM zinc, at least 1,000 PPM and less than 30,000 PPM sulfur, at least 80 PPM and less than 450 PPM Boron;
b. lubricating the internal combustion engine with the composition.
Patent History
Publication number: 20080171677
Type: Application
Filed: Mar 30, 2007
Publication Date: Jul 17, 2008
Inventors: William H. Buck (West Chester, PA), L. Oscar Farng (Lawrenceville, NJ), Douglas E. Deckman (Mullica Hill, NJ), Steven Kennedy (West Chester, PA), Andrew G. Horodysky (Cherry Hill, NJ)
Application Number: 11/731,880
Classifications
Current U.S. Class: With Nitrogen, Sulfur, Or Halogen Compound (508/151)
International Classification: C10M 169/04 (20060101);