Background of the invention Multi-grade engine oils, derived from a combination of low viscosity basestocks and high molecular weight thickeners, viscosity index improvers, and other components have been used for a long time. Synthetic engine oils based onpolyalphaolefins (PAOs) have been shown to demonstrate performance benefits together with cost effectiveness in automotive and other engine applications. In these synthetic oils, as with conventional oils of mineral origin, the viscosity-temperature relationship of the oil is one of the critical criteria which must be considered when selecting the lubricant for a particular application. The viscosity requirements for qualifications as mufti-grade engine oils are described by the SAE Engine Oil Viscosity Classification-SAE J300. The low temperature (W) viscosity requirements are determined by ASTM D 5293, Method of Test for Apparent Viscosity of Motor Oils at Low Temperature Using the Cold Cranking Simulator (CCS), and the results are reported in centipoise (cP). The higher temperature (100° C.) viscosity is measured according to ASTM D445, Method of Test forKinematic Viscosity of Transparent and Opaque Liquids, and the results are reported incentistokes (cSt). Table 1 below outlines the high and low temperature requirements for the recognized SAE grades for engine oils.

Table 1 Engine Oil Viscosity Grade Specifications (SAE J300) Cranking Kinematic SAE Viscosity (cP) at Viscosity (cSt.) Viscosity Temperature (°C.) at 100° C.

Grade Max. Min. Max.

0 W 3250 at-30° 3.8 5 W 3500at-25° 3.8 10 W 3500 at-20° 4.1 15 W 3500 at-15° 5.6 20 W 4500 at-10° 5.6 25 W 6000 at-5° 9.3 20 5.6 <9.3 30 9.3 <12.5 40 12.5 <16.3 50 16.3 <21.9 60 21.9 <26.1 The SAE J300 viscosity grade definitions end at SAE 60 but the scale may be extrapolated in a simple linear manner using the following corretation, which is used in this specification in reference to viscosity grades beyond J300: Table la Extended High-Temperature Viscosity Grades Viscosity Kinematic Kinematic Grade Viscosity (cSt) Viscosity (cSt) Minimum Maximum (Extrapolation beyond SAE J300) 70 26.1 <30 80 30 <35 90 35 <40 100 40 <45 110 45 <50 120 50 <55 130 55 <60 140 60 <65 150 65 <70 In a similar manner, SAE J306c describes the viscometric qualifications for axle and manual transmission lubricants. High temperature (100°C.) viscosity measurements are

performed according to ASTM D445. The low temperature viscosity values are determined according to ASTM D2983, Method of Test for Apparent Viscosity at Low Temperature Using the Brookfield Viscometer and these results are reported in centipoise (cP). Table 2 summarizes the high and low temperature requirements for qualification of axle and manual transmission lubricants.

Table 2 Axle/Transmission Oil Viscosity Specifications SAE Maximum Temperature Kinematic Viscosity at Viscosity for Viscosity 100° C., cSt.

Grade of 150,000 cP., °C. Min Max 70 W-55- 75 W-40 4.1 80 W-26 7.0 85 W-12 11.0 90-13.5 <24.0 140-24.0 <41.0 250 In addition to the viscosity temperature relationship, other properties are, of course, required for an engine oil including resistance to oxidation under the high temperatures encountered in the engine, resistance to hydrolysis in the presence of the water produced as a combustion product (which may enter the lubricating circulation system as a result of ring blow-by) and since the finished oil is a combination of basestock together with additives, these properties should be achieved in the final, finished lubricant so that it possesses the desired balance of properties over its useful life In recent years, considerable attention has been given to the tribological behavior of lubricants under conditions of high shear rate and high pressure. At high shear rates, as in a lubrication contact zone, considerable shear thinning may occur, which results in a decrease in the thickness of the lubricant film separating the relatively moving surfaces with the possibility that inadequate film thickness may be maintained under these conditions. As a counter to this tendency, it would be desirable to provide lubricant compositions which can function effectively under high temperature conditions and which possess good rheological properties to provide adequate film thickness and wear

protection by resisting shear thinning under conditions of high temperature and high shear rate as well as high contact pressure.

As noted above, various combinations of additives with lubricants have been used in the past for the improvement of lubricant properties and in particular, the use of polymeric materials for altering the viscosity or viscosity index of base stocks of mineral and synthetic origin has been well known for a number of years. Polymeric thickeners which are commonly used in the production of multi-grade lubricants typically include hydrogenated styrene-isoprene block copolymers, rubbers based on ethylene and propylene (OCP), polymers produced by polymerization of esters of the acrytate or methacrylate series, polyisobutylene and the like. These polymeric thickeners are added to bring the viscosity of the base fluid up to the level required for the desired grade (high temperature specification) and possibly to increase the viscosity index of the fluid, allowing for the production of multi-grade oils.

The use of high molecular weight thickeners and VI improvers in the production of multi- grade lubricants has, however, some serious drawbacks. First, these improvements are more sensitive to oxidation than the basestocks in which they are used, which may result in a progressive loss of viscosity index and thickening power with use and frequently in the formation of unwanted deposits. In addition, these materials tend to be sensitive to high shear rates and stresses as well as to a high degree of temporary shear the result of which is that temporary or permanent viscosity losses, or reduction of film thickness in bearings may occur. Temporary viscosity losses occurring from shear forces are the result of the non-Newtonian viscometrics associated with the solutions of high molecular weight polymers. As the polymer chains align with the shear field under high shear rates, a decrease in viscosity occurs, reducing film thickness and the wear protection associated with the elastohydrodynamic film. By contrast, Newtonian fluids maintain their viscosity regardless of shear rate. From the point of view of lubricant performance at high temperatures and under the influence of a shear rate condition, it would be desirable to maintain Newtonian rheological properties for the lubricant.

U. S. Patent No. (Watts/Uniroyal) discloses lubricating compositions based on combination of low and high molecular weight PAOs which are stated to provide high viscosity index coupled with improved resistance to oxidative degradation and resistance to viscosity losses caused by permanent or temporary shear conditions. According to the invention description in this patent, the lubricating composition comprises a high viscosity PAO or other synthetic hydrocarbon together with a low viscosity mineral derived oil or PAO or other synthetic hydrocarbon such as alkyl benzene. Optionally, a low viscosity ester and an additive package may be included in the lubricants. While the combination of PAO components of varying molecular weight has been effective in a variety of different applications, further improvements in reducing shear thinning characteristics would be desirable, particularly with increasing demands on engine oil performance. Under modern engine manufacturing trends, engines are operating at higher temperatures and as bearing loadings increase as a result of increased specific power output (kW/I), shear thinning conditions are greatly aggravated.

A new type of PAO lubricant was introduced by U. S. Patents Nos. 4,827,064 and 4,827,073 (Wu). These PAO materials, which are produced by the use of a reduced valence state chromium catalyst, are olefin oligomers or polymers which are characterized by very high viscosity indices which give them very desirable properties to be useful as lubricant basestocks and, with higher viscosity grades, as VI improvers.

They are referred to as High Viscosity Index PAOs or HVI-PAOs. The relatively low molecular weight HVI-PAO materials were found to be useful as lubricant basestocks whereas the higher viscosity PAOs, typically with viscosities of 100 cSt or more, e. g. in the range of 100 to 1,000 cSt, were found to be very effective as viscosity index improvers for conventional PAOs and other synthetic and mineral oil derived basestocks.

We have now found that it is possible to use the HVI-PAOoligomers in combination with oils or mineral origin as well as PAO and other synthetic basestocks in combination with high molecular weight polymers such as viscosity modifiers and VI improvers to produce lubricants which are characterized by viscosity thickening properties. Under high shear rate conditions, as in a highly loaded lubrication contact zone, the good viscoelastic properties of the HVI-PAO component produces unexpectedly high film thickness. The

improved film thickness provides an unexpected degree of wear protection, resisting shear thinning under conditions where high molecular weight polymers lose some or all of their thickening power. Under low-shear or no-shear conditions, as in low pressure oil circulating systems, the high molecular weight polymer which is used in addition to the low molecular weight viscoelastic polymer, provides enhanced bulk oil viscosity due to its thickening properties under conditions where the low molecular weight polymers have little or no thickening power. Multi-grade and widely cross-graded oils can therefore be produced with a combination of good performance properties which are maintained under varying conditions. but are especially notable under conditions of high temperature -high shear rate where they provide unexpectedly good wear protection.

Summary of the Invention The high performance liquid lubricants of the present invention comprise a first polymer and a second polymer of differing molecular weights dissolved in a liquid lubricant basestock of low viscosity. The first polymer, which is of lower molecular weight than the second polymer, possesses high viscoelastic properties as indicated by its unexpectedly high first normal stress difference. This polymer component in the lubricant provides unexpectedly high film thickness and unexpectedly good wear protection under conditions where high molecular weight polymers lose some or all of their thickening power, for example, at high shear rates in lubrication contact zones. The second polymer, which has a higher molecular weight than the first polymer, is characterized by viscosity thickening properties when blended with the liquid basestock used in the lubricant, which may be either mineral-oil derived or synthetic, preferably a PAO.

In preferred compositions of this type, the basestock is typically a wholly synthetic base oil which may be a single PAO or blend of PAOs which provides the designed viscosity in the final blend, together with the other components including the highly viscoelastic polymer which is preferably one of the HVI-PAO olefin polymers referred to above. The highly viscoelastic component will have a viscosity which is greater than that of the PAO basestock but less than that of the higher molecular weight polymer which is typically one of the polymeric thickeners such as the hydrogenated styrene-isoprene block copolymers, ethylene/propylene rubbers, polyisobutylenes or similar materials referred to

above. This polymeric component will typically have a molecular weight in the range from 10,000 to more usually of at least 100,000.

The use of the highly viscoelastic low molecular weight polymer enables the production of very widely cross-graded engine oils, especially oils with a low temperature grading of OW or better. Oils with cross gradings of OW20, OW30, OW40 or even more widely cross graded, for example OW70 or higher may be achieved. Engine oils, cross graded such as OW70 and 25W70, may achieve excellent wear performance even under conditions of high levels of fuel dilution, indicating that the use of the low molecular weight highly viscoelastic component in combination with the high molecular weight polymer component is capable of countering the deleterious oil film thinning effects of fuel dilution on low viscosity base oils. Another particular achievement of this invention is in formulating very low viscosity highly fuel efficient oils with a OW low temperature rating, which have a cross-grading of OW-20 or wider, such as OW-30, which are capable of passing the ASTM Sequence VE wear test, in which high levels of fuel, water, and blow- by contaminants accumulate in the oil during the 12-day, low-temperature test. Although it has previously been possible to pass the high-temperature Sequence III E wear test with a very low-viscosity OW-20 or OW-30 oil, passing the very demanding Sequence V E test had so far been highly elusive.

Drawings The single Figure of the drawings is a graphical representation of the improvement in film thickness achieved by the present synthetic lubricating oils.

Detailed Description General Considerations The present high performance lubricants are highly cross graded engine oils which may be based on mineral derived base oils or synthetic basestocks but the advantages may also be secured in lubricants formulated as axle and transmission oils and industrial oils.

The invention wiil be described with primary reference to engine oils, which represent the prime utility of the invention but it is also applicable to these other classes, as noted. In terms of cross graded engine oils, the lubricants may be separated into two groups. The first group is the group which has a low temperature grade of OW, implying a cold cranking viscosity (ASTM D 5293) of not more than 3250 cP maximum at-30°C. These OW oils necessarily have a very low viscosity at low temperatures in order to meet the extreme low temperature fluidity requirement. Since the low viscosity basestocks required to meet this portion of the specification have a low viscosity at the 100°C temperature used for establishing the high temperature viscosity grade, as well as at actual engine operating temperatures, the OW cross-graded oil is very difficult of achievement. However, by combining the present components, it has been found possible to produce oils conforming to the OW requirement which have excellent wear performance under the actual conditions of use, indicative of good film thickness under shear thinning conditions encountered at high temperatures. Thus, the excellent low temperature oils of the present invention are OW grade oils such as OW20, OW30, OW40 and even more highly cross-graded oils, including OW70, OW80, OW90 and OW100 multi- grade oils. As noted above, the ability to attain Sequence V E wear test performance with a OW-30 rated oil is an excellent indicator of the improved wear performance of the present oils.

The advantages of the present invention may also be secured in other oils with a significant low temperature performance requirement, for example, 5W oils with a high temperature grade of at least 50. For example, cross-graded oils are 5W60,5W70 and higher may be readily achieved in the same way as with the OW oils.

Although indicated by a low temperature performance rating, e. g. OW or W, the present oils are highly satisfactory under high temperature operating conditions and in commercial use, the viscosities characteristic of these low temperature ratings translate into improved fuel economy in actual operation. Thus, in addition to providing ready starting and improved lubrication from start-up, the present oils result in better fuel mileage and overall economy.

One factor which is believed to be significant is that the present oils exhibit improved air release characteristics (ASTM D3427), both in terms of the maximum amount of air entained and in terms of air released within a given time (time in minutes to attain 0.2% and 0.1% air retained in the bulk oil, in the ASTM method). The air retention is beiieved to be associated with the improved viscoelasticity and film thickness achieved with the present lubricants since the elimination of air rapidly from the body of the liquid enables the lubricant fluid properties to dominate. The maximum amount of air entrained at 1.0 minutes (ASTM D3427) of the present oils is less than 3% air, preferably less than 2.5% air, and in the most favorable cases, less than 2.0 %.

Base Oils Because the present oils need to meet the low temperature viscosity requirement, the basestocks used in them will be relatively low viscosity basestocks, generally below 10 cSt at 100°C (all viscosity measurements in the specification are at 100°C unless specified otherwise). Generally, the viscosity of the blended basestocks may be in the range of 2 to 12 cSt. This may be achieved by blending higher viscosity basestocks with basestocks of viscosities below 2 cSt, e. g. about 1.5 cSt, although stocks which are less viscous than this tend to be too volatile, making it difficult to comply with volatility specifications, e. g. NOACK. For example, blends of 2cSt and 4 cSt and or 2 cSt and 6 cSt (nominal) components may be used. Basestocks of 4 to 6 cSt will be found particularly useful for the present types. The viscosity index (VI) of the useful hydrocarbon base stocks are normally 80 or greater, preferably 95 or greater, and most preferably 110 or greater. Further, a minimum 10% of base stock with VI of 110 or greater is highly desirable in order to balance the use of low-VI base stock components.

In some applications, 50% to 90% can be effectively used, and may be preferred.

The low viscosity basestock may be a mineral-derived oil basestock, typically a light neural, or a synthetic basestock. Synthetic hydrocarbon basestocks are preferred, especially the PAOs with viscosities in the range of 1.5 to 12 cSt, generally with VI's of 120 or greater, either in the form of single component or blended PAOs. For example, PAO at 4 cSt has a viscosity index of 120. As alternatives, other synthetic basestocks

may be used, for example, alkylbenzenes, and other alkylated aromatics such as alkylated diphenyl oxides. alkylated diphenyl sulfides and alkylated diphenyl methanes, although these are presently not preferred. In all cases, a viscosity range of about 1.5 to 12 cSt will normally be found satisfactory. Other synthetic basestocks may alto be utilized, for example those described in the seminal work"Synthetic Lubricants", Gunderson and Hart. Reinhold Publ. corp., New York 1962. In alkylated aromatic stocks, the alkyl substituents are typically alkyl groups of about 8 to 25 carbon atoms, usually from 10 to 18 carbon atoms and up to three suchsubstituents may be present, as described for the alkyl benzenes in ACS Petroleum Chemistry Preprint 1053-1058, "Poly n-Alkylbenzene Compounds : A Class of Thermally Stable and Wide Liquid Range Fluids", Eapen et al. Phila. 1984. Tri-alkyl benzenes may be produced by the cyclodimerization of 1-alkynes of 8 to 12 carbon atoms as described in U. S. 5,055,626.

Other alkylbenzenes are described in EP 168 534 and 4,658,072. Alkylbenzenes have been used as lubricant basestocks, especially for low temperature applications (Arctic vehicle service and refrigeration oils) and in papermaking oils ; they are commercially available from producers of linear alkylbenzenes (LABs) such as Vista Chem. Co, Huntsman Chemical Co., as well as Chevron Chemical Co., and Nippon Oil Co. The linear alkylbenzenes typically have good low pour points and low temperature viscosities and VI values greater than 100 together with good solvency for additives. Other alkylated aromatics which may be used when desirable are described, for example, in "Synthetic Lubricants and High Performance Functional Fluids", Dressler, H., chap 5, (R.

L. Shubkin (Ed.) ), Marcel Dekker, N. Y. 1993.

The hydrocracked and hydroisomerized oils represent classes of oils of mineral or synthetic origin which may be used to advantage in the present lubricants. Oils of these types, classified as API Group III basestocks (at least 90 percent saturates, no more than 0.03 percent sulfur, VI at least 120) are currently being produced by the hydrocracking and hydroisomerizing of various hydrocarbon streams of mineral or synthetic origin, including distillates such as vacuum gas oil as well as waxes. The hydrocracked and hydroisomerized waxes are especially favorable since they have high values of viscosity index resulting from their origin as highly paraffinic waxy materials; added to this they are also characterized by low pour points resulting from the

isomerization reactions which take place during the hydroprocessing and which convert the waxy n-paraffins in them to less waxy iso-paraffins of high viscosity index. The resulting hydroprocessed oils therefore possess a desirable combination of properties as lubricant basestocks. A particularly desirable class of hydroisomerized Group III bases stocks are the hydroisomerized Fischer-Tropsch waxes. These waxes, the high boiling point residues of Fischer-Tropsch synthesis, are highly paraffinic hydrocarbons with a very low sulfur content consistent with their synthetic origin. Thehydroprocessing used for the production of such basestocks may use an amorphous hydrocracking/hydroisomerization catalyst, such as one of the specialized lube hydrocracking (LHDC) catalysts or a crystalline hydrocracking/hydroisomerization catalyst, preferably a zeolitic catalyst. Processes for making hydrocracked/hydroisomerized distillates and hydrocracked/hydroisomerized waxes are described, for example, in U. S. Patents Nos. 4,975,177; 4,921,594 and as well as in GB 1 429 494; 1 350 257; 1 440 230 and 1 390 359. Particularly favorable processes are described in EP 464 546 and 464 547. Processes using Fischer-Tropsch wax feeds are described in US and 4,943,672.

Poly Alpha Olefins Poly Alpha Olefins (PAOs) are the preferred low viscosity basestock components of the present compositions. The average molecular weights of the PAOs, which are known materials and generally available on a major commercial scale from suppliers such as Mobil Chemical Company, typically vary from about 250 to about 10,000, although PAO's may be made in viscosities up to about 1,000 cSt (100°C). The PAOs are and typically comprise relatively low molecular weight hydrogenated polymers or oligomers of alphaolefins which include but are not limited to C2 to about C32alphaolefins with the Ce to about C, 6 alphaolefins, such as 1-octene, 1-decene, 1-dodecene and the like being preferred. The preferred polyalphaolefins are poly-1-decene and poly-1-dodecene <BR> <BR> <BR> although the dimers of higher olefins in the range of C14 to C, 8 may be used to provide low viscosity basestocks of acceptably low volatility. The PAOs in the required viscosity range of 1.5 to 12 cSt, are generally predominantly trimers and tetramers of the starting

olefins, with minor amounts of the higher oligomers, depending on the exact viscosity grade and the starting oligomer.

The PAO fluids may be conveniently made by the polymerization of analphaolefin in the presence of a polymerization catalyst such as the Friedel-Crafts catalysts including, for example, aluminum trichloride, boron trifluoride or complexes of boron trifluoride with water, alcools such as ethanol, propanol or butanol, carboxylic acids or esters such as ethyl acetate or ethyl propionate. For example the methods disclosed by U. S. 4,149,178 or U. S. may be conveniently used herein. Other descriptions of PAO synthesis are found in the following U. S. Patents: 3,742,082 (Brennan); 3,769,363 (Brennan); (Heilman) ; (Allphin); 4,367,352 (Watts); 4,413,156 (Watts) ; 4,434,408 (Larkin); 4,910,355 (Shubkin); (Watts); (Theriot).

The dimers of the C, 4 to C, 8 olefins are described in U. S. 4,218,330.

Esters and Other Base Oil Components In addition to the two polymeric components and the low viscosity basestock component, the low viscosity basestock may also comprise other liquid components of comparable viscosity, in the range of 1.5 to 12 cSt, either mineral or synthetic in origin in order to achieve the desired combination of properties in the finished lubricant. For example, when the PAOs, which are highly paraffinic in character, are used as the principal basestock components, it may be desirable to utilize another component which possesses addition chemical functionality (e. g. aromatic, ester, ether, alcool, etc.) in order to confer the desired additive solvency and seal swell characteristics. Certain additives used in oils contain aromatic groups, and for adequate solvency, some aromatic character in the basestock may be required, even though aromatics, generally, do not lead to optimum lubricant performance in themselves. Additive solvency and seal swell characteristics may be secured by the use of esters such as the esters of dibasic acids with monoalkanols and the polyol esters of monocarboxylic acids. Esters of the former type include, for example, the esters of dicarboxylic acids such as phthalic acid, succinic acid, alkyl succinic acid, alkenyl succinic acid, maleic acid, azelaic acid, suberic acid, sebacic acid, fumaric acid, adipic acid, linoleic acid dimer, malonic acid, alkyl

malonic acid, alkenyl malonic acid, etc., with a variety of alcohols such as butyl alcool, hexyl alcool, dodecyl alcohol, 2-ethylhexyl alcohol, etc. Specific examples of these types of esters include dibutyl adipate, di (2-ethylhexyl) sebacate, di-n-hexyl fumarate, dioctyl sebacate, diisooctyl azelate, diisodecyl azelate, dioctyl phthalate, didecyl phthalate, dieicosyl sebacate, etc.

Particularly useful synthetic esters are those which are obtained by reacting one or more polyhydric alcohols, preferably the. hindered polyols such as the neopentyl polyols e. g. neopentyl glycol, trimethylol ethane, 2-methyl-2-propyl-1,3-propanediol, trimethylol propane, pentaerythritol and dipentaerythritol with alkanoic acids containing at least 4 carbon atoms such as the, normally the Csto C30 acids such as saturated straight chain fatty acids including caprylic acid, capric acid, lauric acid, myristic acid, palmitic acid, stearic acid, arachic acid, and behenic acid, or the corresponding branched chain fatty acids or unsaturated fatty acids such as oleic acid.

The most suitable synthetic ester compoents are the esters of trimethylol propane, trimethylol butane, trimethylol ethane, pentaerythritol and/or dipentaerythritol with one or more monocarboxylic acids containing from about 5 to about 10 carbon atoms are widely available commercially, for example, the Mobil P-41 and P-51 esters (Mobil Chemical Company).

While the esters provide satisfactory additive solvency and seal swell characteristics, they are subject to hydrolysis in the presence of small amounts of moisture which accumulate in crank case oils as a product of combustion. Superior performance may be obtained by the use of certain alkylated aromatic compounds in combination with the PAOs for example, alkylbenzenes, alkylmethylenes, alkyldiphenyloxides and diphenylsulfides, of which the alkylated naphthalenes are preferred. Combinations of alkylated naphthalenes and PAOs are described in U. S. 5602086, to which reference is made for a description of alkylated naphthalenes (AN), methods for making them and of AN/PAO combinations.

The basestock component of the present oils will typically be from 50 to 95 weight percent of the total composition (all proportions and percentages set out in this specification are by weight unless the contrary is stated) and more usually in the range of 50 to 85 weight percent. With the low viscosity synthetic oils, the amount of the basestock component is typically from 65 to 90 percent and will tend to be at the higher end of this range for the oils with a low temperature viscosity requirement, e. g. OW, especially when a high viscosity HVI-PAO is used as the amount of the high viscosity material required in the formulation is less. When PAOs are used as the low viscosity component of the basestock in combination with an ester, the relative amounts of PAO and ester will typically be in the range of about 20: 1 to 1: 1, normally 10: 1 to 2: 1. If a low viscosity alkyl aromatic is used in combination with the low viscosity hydrocarbon basestock component. the PAO: alkylaromatic ratio will typically be from 20: 1 to 2: 1, normally 15: 1 to 10: 1 Viscoelastic Polymer The third characteristic component of the present oils which is normally present in a relatively small amount is the low molecular weight polymer with good viscoelastic characteristics. This polymer is marked by a viscoelastic characteristic. Elasticity is a characteristic of polymer-containing fluids, but the level is a function of molecular weight, type and concentration. The potential for bearing journal lubrication benefits from oil elasticity contributed by polymeric VI improvers is well established. See, for example, J.

Inst. Petrol. Tech. 40,191 (1954), ASLE Trans. 4,97 (1961), ASLE Trans. 8,179 (1965), Davies et al"The Rheology of Lubricants", John Wiley, NY 1973, page 65 and Trans.

Soc. Rheol. 20,65 (1976). It has been theorized that the explanation for these benefits is that in the case of full hydrodynamic lubrication, oil elasticity can generate an addition force on the journal in a direction tending to increase the minimum film thickness. This elastic force is at a right angle to the force due to viscosity and is associated with the first normal stress difference, N, induced when viscoelastic fluids are sheared-the higher the value of N,, the higher the elasticity. For the oils of the present invention, it is preferred that the value of N, for the fully formulated oil should be at least <BR> <BR> <BR> 11 and preferably at least 15 kPa, reported at a shear at shear stress (T) = 10 kPa (as

measured by a slit die rheometer, for example a Lodge Stressmeter (Bannatek Co., see SAE Paper No. 872043). In favorable cases, the value of N, may be at least 18kPa or even higher, for example, at least 25 kPa. By contrast, conventionally formulated oils typically have values below about 10 kPa under the same conditions.

The preferred class of materials meeting this requirement is the HVI-PAOoligomers, the type described in U. S. Patent Nos. and 4,827,073, referred to above. Various modifications and variations of these HVI-PAO materials are also described in the following U. S. Patents to which reference is made: 4990709; 5254274; 5132478; 4912272; 5264642; 5243114; 5208403; 5057235; 5104579; 4943383; 4906799. These oligomers can be briefly summarized as being produced by the oligomerization of 1- olefins in the presence of a metal oligomerization catalyst which is a supported metal in a reduced valence state. The preferred catalyst comprises a reduced valence state chromium on a silica support, prepared by the reduction of chromium using carbon monoxide as the reducing agent. The oligomerization is carried out at a temperature selected according to the viscosity desired for the resulting oligomer, as described in U. S. 4,827,064 and 4,827,073. Higher viscosity materials may be produced as described in U. S. and U. S. 5,146,021 where oligomerization temperatures below about 90°C are used to produce the higher molecular weight oligomers. In all cases, the oligomers, after hydrogenation when necessary to reduce residual unsaturation, have a branching index (as defined in U. S. 4,827,064 and 4,827,073) of less than 0.19.

Although characterized as a relatively lower molecular weight and lower viscosity component of the oil (relative to the high molecular weight polymer), this liquid viscoelastic polymer material will generally have a viscosity which is intermediate that of the low viscosity basestock components (e. g. low viscosity PAO, ester and/or alkyl aromatic) and that of the high molecular weight polymer. It will normally have a viscosity in the range of about 12 to 3,000 cSt, e. g. 20 to 1,000 or more usually, 40 to 1, OOOcSt; in many cases, a viscosity from about 100 to 1,000 cSt can be usefully employed. This component will typically comprise about 0.1 to about 25 weight percent, normally 0.1 to 20, e. g. 0.1 to 15, weight percent, of the total finished lubricant. In most cases, at least 1

percent will be present although with the higher molecular weight polymers, less It has been found that the relatively higher molecular weight HVI-PAOoligomers have the most favorable (and unexpected) effect on the air entrainment and air release characteristics (ASTM D-3427) of the oils. For this reason, HVI-PAOs with a viscosity of at least 1,000 cSt, for example, from 1,000 to 3,000 cSt will be preferred for optimal air entrainment and air release properties.

Polymeric Thickener In addition to the low viscosity basestock components and the relatively low molecular weight polymeric viscoelastic component, the lubricants also include a relatively high molecular weight component which has a marked viscosity thickening property when blended with the lower molecular weight components of the basestock. As noted above, these polymeric components typically have a molecular weight from about 10,000 to 1,000,000 normally in the range of 100,000 to They are normally hydrogenated styrene-isoprene block copolymers, rubbers based on ethylene and propylene, high molecular weight acrylate or methacrylate esters, and polyisobutylenes and other materials of high molecular weight which are soluble in the basestocks and which, when added to the basestocks, confer the required viscosity to achieve the desired high temperature viscosity grade e. g. These materials are readily available commercially from a number of suppliers according to type.

The preferred polymeric materials of this class for use in the present formulations are the block copolymers produced by the anionic polymerization of unsaturated monomers including styrene, butadiene, and isoprene. Copolymers of this type are described in U. S. Patents Nos. 5,187,236; 5,268,427; 5,276,100; 5,352,743; 5,359,009; 5,376,722 and Block copotymers may be linear or star type copolymers and for the present purposes, the linear block polymers are preferred. The preferred polymers are the isoprene-butadiene and isoprene-styrene anionic diblock and triblock copolymers. Particularly preferred high molecular weight polymeric components are the ones sold under the designation Shellvis 40, Shelivis 50 and Shellvis 90 by Shell

Chemical Company, which are linear anionic copoiymers; of theseShellvis 50 which is an anionic diblock copolymer is preferred. A less preferred class of anionic block copolymers are the star copolymers such as ShellvisT" 200, SheIIvisT" 260 and Shellvis 300. These high molecular weight solid materials, may conveniently be blended into lubricants in the form of a solution of the solid polymer in other basestock components. The amount of the high molecular weight thickener is typically from 0.1 to 5 percent of the total lubricant, more usually from 0.5 to 3 percent of the total oil, depending upon the viscosity of the basestock components and the desired viscometrics, particularly the high temperature grade required. With relatively low viscosity basestock components, and a relatively high viscosity high-temperature grade requirement, more of the high molecular weight component will be required than if higher viscosity basestock components are used and there is a lower value for the high- temperature grade requirement. Thus, a widely cross-graded oils such as the OW70, OW90 and OW100 will normally require more of the high molecular weight polymer thickener than the less widely cross-graded oils whereas the OW oils with a relatively low high-temperature requirement such as the OW20 oils will need relatively little of this thickening material.

An excellent discussion of types of high molecular weight polymers which may be used as thickeners or VI improvers is given by Klamann in Lubricants and Related Products, Veriag Chemie, Deerfield Beach, FL; ISBN 0-89573-177-0, which also gives a good discussion of other lubricant additives, as mentioned below. Reference is also made "Lubricant Additives"by M. W. Ranney, published by Noyes Data Corporation of Parkridge, N. J. (1973).

Additive Package In addition to the low viscosity basestock components, the viscoelastic polymer and the high molecular weight polymeric thickener, the present oils will also include an additive package to impart or enhance the desired performance properties of the finished oil.

These additives and the overall package will generally be conventional in type for a lubricant of mineral or synthetic origin, depending upon the type of basestock used. The

types of additive which may normally be required include, for example, the following: (1) oxidation inhibitors, (2) dispersants, (3) detergents, (4) corrosion inhibitors, (5) metal deactivators, (6) anti-wear agents, (7) extreme pressure additives, (8) pour point depressants, (9) viscosity index improvers (Vil), (10) seal compatibility agents, (11) friction modifiers and (12) defoamants.

Oxidative stability s provided by the use of antioxidants and for this purpose a wide <BR> <BR> <BR> <BR> range of commercial available materials is available, as noted byKlamann op cit.. The most common types of are the phenolic antioxidants and the amine type antioxidants, of which the latter are preferred. They may be used individually by type or in combination with one another.

The phenolic antioxidants may be ashless (metal-free) phenolic compounds or neutral or basic metal salts of certain phenolic compounds. Typical phenolic antioxidant compouunds are the hindered phenolics which are the ones which contain a sterically hindered hydroxyl group, and these include those derivatives of dihydroxy aryl compounds in which the hydroxyl groups are in the o-or p-position to each other.

Typical phenolic antioxidants include the hindered phenols substituted with C6+ alkyl groups and the alkylene coupled derivatives of these hindered phenols. Examples of phenolic materials of this type 2-t-butyl4-heptyl phenol; 2-t-butyl-4-octyl phenol; 2-t- butyl-4-dodecyl phenol; 2,6-di-t-butyl-4-heptyl phenol; 2,6-di-t-butyl-4-dodecyl phenol; 2- methyl-6-di-t-butyl-4-heptyl phenol; and 2-methyl-6-di-t-butyl-4-dodecyl phenol.

Examples of ortho coupled phenols include: 2,2'-bis (6-t-butyl-4-heptyl phenol); 2,2'-bis (6- t-butyl4-octyl phenol); and 2,2'-bis (6-t-butyl-4-dodecyl phenol).

Non-phenolic oxidation inhibitors which may be used include the aromatic amine antioxidants and these may be used either as such or in combination with thephenolics.

Typical examples of non-phenolic antioxidants include: alkylated and non-alkylated aromatic amines such as the aromatic monoamines of the formula R3R4R5N where Ri ils an aliphatic, aromatic or substituted aromatic group, R 4 is an aromatic or a substituted aromatic group, and R5 is H, alkyl, aryl or R6S (O) xR where R6 is analkylene, alkenylene, or aralkylene group, R'is a higher alkyl group, or an alkenyl, aryl, oralkaryl group, and x

is 0,1 or 2. The aliphatic group R3 may contain from I to about 20 carbon atoms, and preferably contains from 6 to 12 carbon atoms. The aliphatic group is a saturated aliphatic group. Preferably, both R3 and R4 are aromatic or substituted aromatic groups, and the aromatic group may be a fused ring aromatic group such asnaphthyl. Aromatic groups R3 and R4 may be joined together with other groups such as S.

Typical aromatic amines antioxidants have alkyl substituent groups of at least 6 carbon atoms. Examples of aliphatic groups include hexyl, heptyl, octyl, nonyl, and decyl.

Generally, the aliphatic groups will not contain more than 14 carbon atoms. The general types of amine antioxidants useful in the presentcompostions include diphenylamines, phenyl naphthylamines, phenothiazines, imidodibenzyls and diphenyl phenylene diamines. Mixtures of two or more aromatic amines are also useful. Polymeric amine antioxidants can also be used. Particular examples of aromatic amine antioxidants useful in the present invention include: p, p'-dioctyldiphenylamine; octylphenyl-beta- naphthylamine; t-octylphenyl-alpha-naphthylamine; phenyl-alphanaphthylamine; phenyl- beta-naphthylamine; p-octylphenyl-alpha-naphthylamine; 4-octylphenyl-l-octyl-beta- naphthylamine.

Normally, the total amount of antioxidant will not exceed 10 wt. percent of the total composition and normally is below about 5 wt. percent, typically from 1 to 2 wt. percent.

Dispersants are also a known group of functional additives for lubricating oils, being used to maintain oxidation products in suspension in the oil, preventing accumulations of debris which could score bearings, block oilways and cause other types of damage as welll as preventing depoist formation and inhibiting corrosive wear by the neutralization of acidic combustion products. Dispersants may be ash-containing or ashless in character, of which the ashless variety are preferred. Chemically, manydispersants may be characterized as phenates, sulfonates, sulfurized phenates, salicylates, naphthenates, stearates, carbamates, thiocarbamates, phosphorus derivatives. A particularly useful class of dispersants are the alkenylsuccinic derivatives, typically produced by the reaction of a long chain substituted alkenyl succinic compound, usually a substituted succinic anhydride, with a polyhydroxy or polyamino compound. The long

chain group constituting the oleophilic portion of the molecule which confers solubility in the oil, is normally a polyisobutylene group. Many examples of this type of dispersant are well known commercially and in the literature. Exemplary U. S. patents describing such disperants are 3,172,892 ; 3,2145,707; 3, 219,666; 3,316,177; 3,341,542; 3,444,170; 3,454,607; 904; 3,632,511; 3,787,374 and 4,234,435. Other types of dispersant are described in U. S. Patents Nos. 3,036,003; 3,200,107; 3,254,025; 3,275,554; 3,438,757; 3,454,555; 3,565,804; ; 3,725,480; 3,726,882; 4, 454,059; 3,329,658; 3,449,250; 3,519,565; 3,666,730; 3,687,849; 4,100,082; 5,705,458. A further description ofdispersants may be found, for example, in EP 471 071, to which reference is made for this purpose.

The detergents are also an important additive component, serving to maintain overall cleanliness. Chemically, many detergents are similar to the dispersants as noted by Klamann and Ranney op cit. Ranney discloses a number of overbased metal salts of various sulfonic acids which are useful as detergents/dispersants in lubricants. The book entitled"Lubricant Additives", C. V. Smailheer and R. K. Smith, published by the Lezius-Hiles Co. of Cleveland, Ohio (1967), similarly discloses a number of overbased sulfonates which are useful as dispersants/detergents.

Corrosion inhibitors or metal suppressors are not normally required in the present compositions but may be optionally be added, depending on the type of metals to be encountered in operation. A wide variety of these are commercially available; they are referred to also in Klamann, op. cit.

The antiwear agents typified by the zinc dialkyl dithiophosphates such as the zinc di (iso- hexyl) dithiophosphate are preferably added to the present compositions since, although the combination of low and high molecular weight polymers in the low viscosity basestocks acts to increase film thickness in elastohydrodynamic conditions, the addition effect of the additive is desirable under severe operational conditions.

Pour point depressants and viscosity index improvers (Vil) will not normally be required in the present oils because the low viscosity basestocks usually posses a sufficiently low

pour point that no further modification of this property is required. However, conventional pour point improvers may be added as desired. The high molecular weight polymer component acting as a viscosity modifier and also as a VI improver will normally, in combination with the highly viscoelastic HVI-PAO component, confer a sufficiently high value of VI on the oil that no further augmentation is required but again, conventional additives of this type may optionally be used. Both these types of additive are described in Klamann, op cit.

Seal compatibility agents will normally be required as the highly paraffinic nature of the preferred basestocks makes it necessary to use this additive to meet seal compatibility specifications. Additives of this type are commercially available, for example, as various aromatic esters, and may be used in conventional amounts, typically from 0.1 to 5 percent of the total lubricant, usually from 0.5 to 2 percent, depending on the actual composition.

The friction modifiers (friction reducing agents) are a desirable class of additives and again, are commercially available as various fatty acid and/or ester derivatives. They also are described in Klamann, op cit. Glycerol esters such as the glycerol mono-oleates are a preferred class of friction modifiers for the present lubricants; they are suitably used in an amount from 0.1 to 1 percent of the total lubricant.

Defoamants, typically silicone compounds, are commercially available and may be used in conventional minor amounts along with other additives such as demulsifiers; usually the amount of these additives combined is less than 1 percent and often less than 0.1 percent.

Example 1 A number of oils were formulated to varying viscosity grades (SAE, and extended) to illustrate the cross-graded lubricants with excellent low temperature performance according to the present invention. Compositions are weight percentages.

Table 4a OW MULTIGRADE ENGINE OILS Example No. 1-1 1-2 1-3 1-4 Viscosity Grade OW-20 OW-30 OW-50 OW60 Polymeric Thickener 1 0.36 0.84 Polymeric Thickener 2 2.40 2.20 Polymeric Thickener 3 HVI-PAO, 150 cSt 2.0 2.0 10.00 10.00 PAO, 5.6 cSt 10.0 PAO, 4 cSt 63.37 73.58 25.37 50.57 PAO, 1.7 cSt 25.00 Ester--25.00 25.00 Alkyl Aromatic 8.46 7.05 Performance Additives 15.81 16.53 12.23 12.23 Package KV @ 100C (cS) 20.67 23.10 CCS @-30 C (cP) 2600 3000 1500 2700 HTHS @ 150 C (cP) 2.90 3.00 4.73 5.42 Notes: Polymeric Thickener 1 Shellvis 50 Polymeric Thickener 2 Shellvis 260 Polymeric Thickener 3 SheilvisTM 300 Table 4b OW MULTIGRADE ENGINE OILS Example No. 1-5 1-6 1-7 1-8 1-9 Viscosity Grade OW70 OW-70 OW-80 OW-90 OW-100 Polymeric Thickener 1 2.74 Polymeric Thickener 2 3.30 3.36 Polymeric Thickener 3 2. 08 3.12 HVI-PAO, 150 cSt 2.00 10.00 10.00 10.00 10.00 PAO, 8 cSt 1.00 PAO, 5.6 cSt 1.00 PAO, 4 cSt 53.89 50.69 24.47 24.41 24.65 PAO, 25.00cSt 25.00 25.00 EsterEster25.00 25.00 25.00 25.00 25.00 Performance Additives 14.37 12.23 12.23 12.23 12.23 Package KV @ 100C (cS) 26. 93 27. 57 34.04 36.60 44.57 -30CCCS@ (cP) 2000200019502900 HTHS @ 150 C (cP) 5.51 5.40 6.37 6.36 6.32

Notes: Polymeric Thickener 1 ShelivisT"50 Polymeric Thickener 2 Sheilvis 260 Polymeric Thickener 3 Sheiivis 300 Example 2 A synthetic PAO-based 5W-60 oil was prepared as shown in Table 5 below.

Table 5 5W-60 Engine Oil Polymeric Thickener 1 2.40 HVI-PAO, 150 cSt 8.00 PAO, 4 cSt 49.74 Ester 22.80 Performance Additives 17.06 KV @ 100C (cSt) 24.0 CCS @-25 C (cP) 2980 HTHS @ 150 C (cP) 5.60

Example 3 This example demonstrates the potential for achieving a pass on the ASTM Sequence V-E test, using a combination of the three synthetic components in the lubricant. The oil was formulated as a OW-30 oil but the concept would also be applicable for OW-20 cross grade with appropriate formulation changes. The test results are shown in Table 6 below.

Table 6 Wear Protection Performance of in Sequence VE Engine Test Example No. 3-1 3-2 Viscosity Grade: OW-30 OW-30 Formulation (Wt. %) 0.900.78ShellvisTM50 HVI-PAO 150 cSt-2.00 Synthetic Base Oils 84.27 82.39 (PAO/Aromatic; 9/1) Performance Additive 14.83 14.83 Package Physical Pro erties KV @100C (cSt) D445-5 9.8 9.8 KV @40C (cSt) D445-3 51.0 51.4 Viscosity Index D-2270 181 179 CCS @-30 C (cP) D5293-6 1980 2110 HTHS @ 150 C (cP) D4683 2.88 2.89 Sequence VE Test Limits Avg. Engine Sludge 9.0 Min 7. 1 9.5 Rocker Cover Sludge 7.0 Min 5. 5 9. 1 Piston Skirt Varnish 6.5 Min 7. 5 7.2 Avg. Engine Varnish 5.0 Min 6. 0 5. 8 Cam Lobe Wear, pm Maximum 380 Max 415 28 Average 127 Max 189 18 Oil Screen Clogging, % 20 Max 0 0 Assessment: Fail Pass

These results show that the use of the three components of the present oils combine to provide the required characteristics for the Sequence V-E wear test pass.

Example 4 This example illustrates the effect of the HVI-PAO oligomer viscosity on the air entrainment and air release characteristics of the lubricant. Oils were formulated to a 5W-30 grade and tested for air release characteristics by ASTM D-3427. The results are shown in Table 7 below.

Table 7 Formulation Effects on D3427 Air Release Example No 4-1 4-2 4-3 4-4 4-5 Viscosity Grade 10W-30 5W-30 5W-30 5W-30 5W-30 PAO 1 OOcSt 20.25 HVI-PAO 150 cSt 20.00 HVI-PAO 300 cSt 15.55 HVI-PAO1000 cSt 9.82 HVI-PAO 3000 cSt 6.82 PAO 4cSt 47.32 47.57 52.02 57.75 60.75 PAO 6cSt 1.00 1. 00 1.00 1.00 1.00 Ester 17.00 17.00 17.00 17.00 17.00 Additive Package 14.43 14.43 14.43 14.43 14.43 Table 7 (cont'd) KV @100C (cSt) 11.78 11.50 11.7 11.58 11.7 CCS @-25 C (cP) 4630 3090 3150 2440 2100 HTHS @ 150 C (cP) 3.92 3.91 4.01 3.93 3.84 ASTM D3427 Max. % Air @ 1 min. 2.51 1.92 1.50 1.60 0.25 Time (min) to 0.1% Air 14.63 11.38 10.10 10.10 1.78 Time (min) to 0.2% Air 12.59 10.27 8.50 8.11 1.25

Example 5 This example illustrates the effect of the linear high molecular weight polymer on the air entrainment and air release characteristics as compared to the star type polymer. The results of testing oils formulated to 5W-50 with a combination of high molecular weight thickener, PAO base oil and HVI-PAO component, are shown in Table 8 below.

Table 8 5W-50 Cross Grade Oils; D3427 Air Release Example No. 5-1 5-2 5-3 5-4 ShellvisT" 50 1.75 1.75 SheliViSTm 260 1. 48 1.48 HVI-PAO 150 cSt 20. 00 20.00 HVI-PAO 3000 cSt 6. 00 6.50 PA06 0.80 0.80 0.80 0.80 Pua0452.23 66.23 52.50 66.00 Ester 13.68 13.68 13.68 13.68 Performance Additive 11.54 11.54 11.54 11.54 Package KV @100C (cS) 19.75 20.49 20.39 20.79 CCS @-25 C (cP) 3500 2200 3350 2200 HTHS @ 150 C (cP) 5.58 5.37 5.82 5.57 ASTM D3427 Max. % Air @ 1 min. 2.56 2.67 3.39 3.79 Time (min) to 0.1% Air 18.65 12.95 20.94 14.32 Time (min) to 0.2% Air 15.62 10.84 16.98 13.06

The results in Table 8 above show that the air entrainment and air release characteristics are better with the linear polymer thickener (e. g. compare 5-1 versus 5-3), and that the higher viscosity HVI-PAO component promotes faster air release with a given polymer thickener (e. g. compare 5-1 versus 5-2).

Example 6 This example demonstrates the improvement in film thickness which may be achieved by the use of the present combination of components. Two oils were formulated to SAE grade OW-20 as shown in Table 9 below, one oil containing a HVI-PAO (150 cSt) component and one without. The film thicknesses of the oils under EHL conditions were then measured in a point contact (ball-on-disk) test rig using an optical detector (Reference:"The Measurement and Study of Very Thin Lubricant Films in Concentrated Contacts,"by G. J. Johnston, R. Wayte, and H. A. Spikes, Tribology Transactions, Vol. 34 (1991), 2,187-194.). The results are shown graphically in Figure 1.

Table 9 SAE OW-20 Engine Oils xample No. 6-1 6-2 ormulation (Wt. %) helivis 501 0. 37 0.36 VI-PAO 150 cSt-2. 00 ynthetic Base Oils 83.82 81.83 (PAO/Aromatic; 9/1) dditive Package 15.81 15.81 hysical Characteristics V @100C (cSt) 445-5 8.3 8.6 V@40C (cSt) 445-3 43.4 45.9 iscosity Index 169 169 CS @-30 C (cP) 5293-6 2310 2590 THS @ 150 C (cP) 4683 2.71 2.64 The figure shows the effectiveness of including the HVI-PAO component in the present oils. The Figure 1 plots the film thickness (nm) against speed in the test rig for the OW- 20 oil containing the HVI-PAO component and the other OW-20 oil. The plot shows that at lower speeds in the regime of elastohydrodynamic lubrication, the high elasticity polymer boosts the effective film thickness, thus reducing wear effectively in this regime.

At higher speeds, however, in the hydrodynamic lubrication regime, the conventional film properties are sufficient to ensure adequate film thickness.

Example 7 A comparison of viscoelasticity is provided by the following comparative formulations to varying viscosity grades.

Table 10 ViscoElasticity Performance of Oils Example No. 7-1 7-2 7-3 7-4 7-5 Viscosity Grade-5W-40 OW-30 5W-30 OW-20 OW-30 Formulation (Wt.% SheIIvisT""50 1. 9 Acryloid 956 8.5 4.5 HVI-PAO 1000 cSt 8.00 HVI-PAO 3000 cSt 6. 00 Synthetic Base Oils 84.45 77.85 81.85 78.35 80.35 (PAO/Ester; 3/1) Additive Package 13.65 13.65 13.65 13.65 13.65 Ph sical Characteristics KV @100C (cSt) D445-5 14.4 11.9 10.9 9.2 10.0 KV @40C (cSt) D445-3 71.8 55.4 60.4 45.6 48.2 Viscosity Index 210 173 188 199 CCS @-25 C (cP) D5293-5 3000 CCS @-30 C (cP) D5293-6 1880 2410 2600 2520 CCS @-35 C (cP) 3210 HTHS @ 150 C (cP) D4683 3.3 3.2 3.3 3.2 3.3 Viscoelasticity First Normal Stress Difference, N, 4 8 11 18 28 (kPa), @ Shear Stress = 10 kPa

In Table 10 above, comparison of Formulations 7-2 and 7-5, both OW-30 grade, shows that the HVI-PAO component is associated with a high value of viscoelasticity which, in turn, can be correlated with improved film thickness in the fully formulated lubricant.

Formulation 7-4 is also demonstrative of the high values of viscoelasticity associated with the HVI-PAO component.

Example 8 This Example illustrates the potential for obtaining improved air entrainment and air release characteristics in a widely cross-graded oil containing the HVI-PAO component. Two oils were formulated to viscosity grade OW-70 using a linear and a star polymer type thickener.

Table 11 Wide Cross Grade Oils, OW-70; D3427 Air Release Example No. 8-1 8-2 Viscosity Grade OW-70 OW-70 Sheilvis M 50 2. 74 Shelivis 260 2. 27 HVI-PAO 150 cSt 2.00 2.00 PAO8 1. 00 1.00 PAO6 1.00 1. 00 PAO4 53. 89 54.36 Ester 25. 00 25.00 Performance Additives 14.37 14.37 Package KV @100C (cS) 26.93 26.85 CCS @-30 C (cP) 3110 3080 HTHS @ 150 C (cP) 5.51 6.05 ASTM D3427,75 C Max. % Air @ 1 min. 1.42 1.96 Time (min) to 0.1 % Air 7.55 9.79 Time (min) to 0.2% Air 6.76 8.60

Example 9 This Example illustrates the potential for obtaining improved air entrainment and air release characteristics in a widely 10W-60 cross-graded oil containing the HVI-PAO component. These oils were formulated using a linear and a star polymer type thickener, alone or in combination.

Table 12 Wide Cross Grade Oils, 10W-60; D3427 Air Release Example No. 9-19-49-59-2 Viscosity Grade 10W-60 10W-60 10W-60 10W-60 10W-60 2.191.101.10ShellvisTM50 SheiIvisT""260 1. 52 0.76 ShelivisT 300 1. 30 0.65 HVI-PAO 150 cSt 20. 00 20. 00 20. 00 20. 00 20.00 PA06 1. 00 1. 00 1. 00 1. 00 1. 00 46.0546.2745.7145.81PAO445.23 Ester 17. 16 17. 00 17. 00 17. 00 17.01 Performance Additive 14.43 14. 43 14. 43 14. 43 14.43 Package KV @ 100C (cS) 25.36 24. 90 24. 98 25. 08 25. 05 CCS @-20 C (cP) 2370 2490 2620 2730 2770 HTHS @ 150 C (cP) 6.51 6. 32 6. 23 6. 64 6.71 ASTM D3427 Max. % Air @ 1 min. 1. 21 2.26 3.34 2.71 2.78 Time (min) to 0.1 % Air 15.78 22. 13 28. 06 18. 65 23.61 Time (min) to 0.2% Air 13.88 18. 58 23. 71 15. 62 19.70