Lubricant compositions with improved viscosity index

Abstract

Disclosed are lubricant compositions containing adducts of an amine with a phosphate ester of the formula: ##EQU1## wherein R is hydrogen or alkyl having up to 25 carbon atoms in the chain, R' is hydrogen or alkyl having up to 7 carbon atoms except only one of R and R' can be hydrogen or octyl.

Description

This invention relates to the preparation of novel and useful lubricating compositions. More particularly, the invention concerns lubricating oil compositions comprising a base mineral oil and a specified adduct of an amine with a phosphate ester whereby the viscosity index of the oil is substantially improved.

In the prior art, U.S. Pat. No. 2,983,678/9 disclosed the use of rare earth salts of ethyl oleyl acid as viscosity index (VI) improvers. Undesirably, formulations containing these additives proved deficient in storage stability, reporducibility of viscosities and compatibility with conventional lubricating oil additives. Additionally, these salts, being partly inorganic, are not suitable for use in ashless or low metal formulations.

In accordance with the invention, there are provided improved lubricating compositions comprising a major proportion of an oil of lubricating viscosity and from 0.01 to 10 percent by weight thereof of at least one adduct of an amine with a phosphate ester of the formula: ##STR1## wherein R is hydrogen, alkyl having up to 25 carbon atoms and R' is hydrogen or alkyl having up to 7 carbons, except that only one of R or R' can be hydrogen or octyl.

The phosphate ester should be present preferably in 0.1 to 1.0 weight percent of base oil and may be used in proportions of 0.01 to 10.0 weight percent. The amine should be present in an amount stoichiometrically equivalent to phosphate ester and preferably in a proportion such that three moles of amine are present per mole of phosphate. The operable range includes 1.0 to 10.0 moles of amine per mole of phosphate ester.

Both naphthenic and paraffinic distillates can be treated by the method of the invention; for best results, these should be 20 weight or lighter, since relatively larger amounts of adduct are needed in heavy oils. Naphthenic and paraffinic residual stocks, undistilled crudes, extracts from solvent refining also respond to the method of the invention. Oils which have already been subjected to deasphalting, dewaxing, solvent refining, clay contacting, acid treating, hydrogenation, or any combination of the foregoing processes are amenable to the method of the invention.

The adduct may be prepared in concentrated form in any convenient base oil or the amine and phosphate ester may be added to the bulk of the oil to be treated separately. The former method is preferred. If the former method is used, the amine-ester concentrate is best heated to 225.degree.F. before being added to the base oil. This assures complete solution of the amine and phosphate in the concentrate.

The amine is of the general formula: ##STR2## wherein the substituents can be either hydrogen, alkyl or aryl groups having up to 30 carbons atoms. As shown by the data of Table V, below, the nature of the amine is not critical. Thus typical amines include methyl benzyl amine, isobutylamine N-cyclohexylpiperidine and furfuryl amine. Only adducts of ethyl oleyl acid orthophosphate have found to give reproducible blend viscosities.

The unobvious and unexpected results obtained with the invention are disclosed hereinbelow.

In Table I below there are shown the effects of amine-phosphate ester adducts on the viscosity and viscosity index of some representive base oils: a 300 second naphthene distillate a 5 weight solvent neutral oil, a 20 weight solvent neutral oil and a dewaxed (but unrefined) 20 weight wax Distillate.

In all cases, a liquid concentrate of amine and phosphate ester was prepared and added volumetrically to the base oil in question.

Ethyl oleyl acid orthophosphate (3.1 grams) and methyl benzyl amine (3 ml) were combined in 100 ml of 55 Pale Oil* and heated with stirring to 225.degree.F. Ten or twenty milliliter portions of the cooled concentrate were added to the base oil, and the resultant blend stirred at room temperature for a few minutes.

*55 Pale Oil is here and hereafter used to designate a 55 SUS viscosity at 100.degree.F. naphthene pale oil.

The slight decrease in 100.degree.F. viscosity, which will be noted for the resultant blends, is entirely attributable to the light carrier oil used to prepared the concentrate.

In Table II, below there are summarized the effect of ethyl oleyl acid orthophosphate alone, methyl benzyl amine alone, and the amine-phosphate combination on the viscosities and viscosity indices of 300 SUS at 100.degree.F viscosity naphthene distillate. All were added in light carrier oil; this light oil comprises 5 percent of the resultant blend.

The explanatory data of Table III, shows that other amines of various structural types may be effectively used with ethyl oleyl acid orthophosphate as a viscosity index improver.

A major objection to the use of rare earth salts of dialkyl acid orthophosphates was the widely varying viscosities and viscosity indices obtained from presumably identical blends of salts and base oil. To demonstrate the superiority of the amine-phosphate adduct in this respect, four blends of unrefined, dewaxed 20 weight was distillate were treated with sufficient ethyl oleyl acid orthophosphate methyl benzyl amine adduct to bring about a viscosity index increase of about 50 percent. Two samples were taken from each blend and the viscosities of each of the eight samples determined; these are listed in Table IV. Satisfactory agreement is observed between samples from the same blends and among various blends.

TABLE I__________________________________________________________________________EFFECT OF ETHYL OLEYL ACID ORTHOPHOSPHATE-ORGANIC AMINE COMPLEXES ONVARIOUS OILS__________________________________________________________________________ Ethyl Oleyl Quantity Acid Ortho- Methyl Benzyl Carrier Quantity of Kinematic Viscosity, csBase Oil (ml) phosphate (g) Amine (ml) Oil Carrier (ml) 100.degree. 210.degree. VI__________________________________________________________________________300 Pale Stock -- -- -- -- -- 66.44 6.46 20300 Pale Stock 200 0.31 0.3 55 Pale 10 60.73 7.34 88*Solvent Neutral-5 -- -- -- -- -- 20.42 3.92 91Solvent Neutral-5 200 0.31 0.3 55 Pale 10 19.70 5.19 231*Solvent Neutral -20 -- -- -- -- -- 73.06 8.27 88Solvent Neutral -20 200 0.62 0.6 55 Pale 20 57.92 10.13 176**Dewaxed WD-20 -- -- -- -- -- 177.04 12.24 49Dewaxed WD-20 200 -- 0.3 55 Pale 10 148.16 11.06 51Dewaxed WD-20 200 0.31 0.6 55 Pale 10 148.75 11.58 62*Dewaxed WD-20 200 0.62 55 Pale 20 129.34 11.32 77*__________________________________________________________________________ *Average 8 runs **Average 6 runs TABLE II__________________________________________________________________________EFFECTS OF ETHYL OLEYL ACID ORTHOPHOSPHATE AND METHYL BENZYL AMINE ON 300PALE STOCK__________________________________________________________________________ Phosphate Amine Quantity Kinematic Visc.Base Oil Quantity (ml) (g) (ml) Carrier (ml) 100.degree.F. 210.degree.F. VI__________________________________________________________________________300 Pale Stock -- -- -- -- -- 66.44 6.46 20300 Pale Stock 200 -- -- 55 Pale Oil 10 58.80 6.07 26300 Pale Stock 200 0.31 -- 55 Pale Oil 10 62.76 6.26 21*300 Pale Stock 200 -- 0.3 55 Pale Oil 10 59.75 6.13 24**300 Pale Stock 200 0.31 0.3 55 Pale Oil 10 60.73 6.46 88***__________________________________________________________________________ *Average 7 Runs **Average 6 Runs ***Average 8 Runs TABLE III__________________________________________________________________________EFFECTIVENESS OF ETHYL OLEYL ACID ORTHO PHOSPHATE WITH VARIOUS AMINESWITHRESPECT TO VI IMPROVEMENT OF 300 PALE STOCK__________________________________________________________________________ Quantity Quantity kinematic Viscosity, csBase Oil (ml) EOP* (g) Amine (ml) 100.degree. 210.degree. VI__________________________________________________________________________300 Pale Stock -- -- -- -- 66.44 6.46 20300 Pale Stock 1000 3.1 .alpha.-methylbenzyl amine 3 68.99 9.97 138300 Pale Stock 1000 3.1 N-cyclohexyl piperidine 3 112.52 16.42 168300 Pale Stock 1000 3.1 Isobutyl amine 3 81.69 12.05 152300 Pale Stock 1000 3.1 Furfuryl amine 3 84.33 13.92 181__________________________________________________________________________ *Ethyl oleyl acid orthophosphate TABLE IV______________________________________REPRODUCIBILITY OF VISCOSITY INDEX IMPROVEMENT______________________________________A. Concentrate containing 3.1 grams of ethyl oleyl acid orthophosphate and 3 ml methyl benzyl amine in 100 ml of 55 Pale Oil is prepared at 275.degree.F. Ten milliliter portions of concentrate are added to each of four 200 ml portions of unrefined, dewaxed 20 weight wax distillate. Each sample submitted for duplicate determination of 100.degree.F. and 210.degree.F. kinematic viscosity:______________________________________ Viscosity at 100.degree. 210.degree. VIBase Oil 177.04 12.24 49Blend 1 148.98 11.49 61 148.73 11.60 62Blend 2 148.46 11.56 62 150.04 11.67 63Blend 3 148.92 11.70 64 148.22 11.55 61Blend 4 148.78 11.60 62 148.90 11.49 60B. Concentrate prepared in A is added in 20 milliliter portions to/200 ml portions of the same base oil. Two samples of each blend tested:______________________________________Blend 1 128.98 11.25 76 128.66 11.36 78Blend 2 129.47 11.37 78 129.49 11.38 78Blend 3 129.53 11.29 76 130.26 11.35 76Blend 4 129.05 11.30 76 129.32 11.25 75______________________________________ TABLE V__________________________________________________________________________VI IMPROVEMENT OF 300 PLATE STOCK:EFFECT OF AMINE STRUCTURE IN ETHYLOLEYL ACID ORTHOPHOSPHATE ADDUCTS__________________________________________________________________________ EOAP, Vol. Kin. Vis, csAmine Wt % Wt % Carrier % 100.degree.F. 210.degree.F. VI__________________________________________________________________________None -- -- -- -- 66.44 6.46 20Oleylamine ("Armeen-O") 0.15 0.17 -- -- 68.05 7.98 90.alpha.-Methylbenzylamine 0.31 0.30 -- -- 68.99 9.97 138N-cyclohexylpiperidine 0.31 0.30 -- -- 112.52 16.42 168Isobutylamine 0.31 0.30 -- -- 81.69 12.05 152Furfurylamine 0.31 0.30 -- -- 84.33 13.92 181None -- -- 55 Pale Oil 13 48.21 5.48 23 Filt.__________________________________________________________________________

To show shear stability and storage stability solvent neutral oil 5 blend containing the EOAP -.alpha.- methylbenzylamine adduct was studied. It underwent no decrease in 100.degree.F viscosity under the conditions of the 20-pass Fuel Injector Shear Stability Test. Some increase in 210.degree.F. viscosity did result; viscosity index across the test underwent a nominal increase, although both sheared and unsheared blends were too high to calculate in the normal manner. These data are summarized in Table VI.

The SNO-5, EOAP, MBA blend listed in Table V was tested at the end of 6 and 171 days standing at room temperature. Some decrease in 210.degree.F. viscosity occurred after the longer period. Viscosity index remained above 250 in all cases. Data are included in Table VI.

TABLE VI__________________________________________________________________________SHEAR AND STORAGE STABILITY OF SNO-5 CONTAININGETHYL OLEYL ACID ORTHIOPHOSPHATE-.alpha.=METHYLBENZYLAMINE__________________________________________________________________________ADDUCT Percentage Kinematic Viscosity Decrease in 100.degree.F, cs 210.degree.F., cs VI 100.degree.F. Viscosity__________________________________________________________________________1. SNO-5 20.42 3.92 912. SNO-5 plus 5.0 vol% 55 Pale Oil 19.54 3.80 883. SNO-5 plus EOAP (0.155 wt%), 20.01 7.32 250methylbenzylamine (0.16 wt%), 5.0 vol% 55 Pale Oil4. Above, after 20-pass FISST (sample 1) 20.36 8.07 3005. Above, after 20-pass FISST (sample 2) 20.35 8.80 300 06. No. 3, After six days at room temperature 20.23 6.82 300 07. No. 3, After 171 days at room temperature 20.11 6.77 300__________________________________________________________________________

Table VII, below, shows the VI enhancing effect of other adducts according to the invention. As pointed out previously, however, only adducts of ethyl oleyl acid orthophosphate give reproducible blend viscosities. The other adducts, in common therewith, have utility as pour point modifiers, oil thickening agents and as oil spill coagulates.

TABLE VII__________________________________________________________________________VI-ENHANCING EFFECT: VARIOUS AMINE PHOSPHATE ADDUCTS__________________________________________________________________________ Kinematic Viscosity, csAcid Phosphate Wt. % Amine Vol. % 100.degree.F 210.degree.F VI__________________________________________________________________________In 300 Pale Stock300 Pale Stock 66.44 6.46 20300 Pale Stock containing 4.8 vol. % 55 Pale Oil(used in asterisked cases below) 58.80 6.07 26*amyl 0.15 hexyl 0.15 59.46 6.09 23amyl 0.31 oleyl 0.30 68.47 6.62 24butyl 0.15 isobutyl 0.15 68.20 6.60 24*butyl 0.15 hexyl 0.15 59.66 6.14 25butyl 0.31 oleyl 0.30 68.06 6.63 26*isooctyl 0.15 isobutyl 0.15 60.55 6.19 25*isooctyl 0.15 .alpha.-methylbenzyl 0.15 60.49 6.16 23isooctyl 0.31 oleyl 0.30 68.02 6.64 27oleyl 0.31 isobutyl 0.30 68.22 6.64 26*oleyl 0.15 hexyl 0.15 59.98 6.10 21phenyl 0.15 isobutyl 0.15 67.82 6.49 18phenyl 0.31 oleyl 0.30 68.68 6.59 24stearyl 0.31 isobutyl 0.30 68.74 6.54 18stearyl 0.31 N-cyclohexylpiperidine 0.30 75.82 6.50 <0 ck 75.54 10.83 43 ck 74.03 6.71 11stearyl 0.30 ethylhexyl 0.30 67.91 6.58 23stearyl 0.31 N,N-dimethylbenzyl 0.30 68.99 7.40 67 ck 68.27 7.32 66 ck 68.04 6.54 20 ck 67.54 6.51 22 ck 68.01 6.57 22stearyl 0.30 dipropyl 0.30 79.11 6.77 <0stearyl 0.30 furfuryl 0.30 68.18 6.72 32stearyl 0.15 hexyl 0.15 60.02 6.14 20*stearyl 0.30 N-methylaniline 0.30 67.52 6.56 23stearyl 0.30 methylcyclohexyl 0.30 67.64 10.71 159stearyl ck 67.60 5.22 <0 ck 68.27 7.36 67 ck 73.33 6.00 <0Stearyl 0.30 oleyl 0.30 68.70 6.56 19Stearyl 0.30 2-picoline 0.30 69.96 10.84 156 ck 69.69 6.88 38 ck 71.16 6.62 14Stearyl 0.30 3-picoline 0.30 70.36 6.49 8Stearyl 0.30 4-picoline 0.30 70.54 6.58 14In "SNO-10" (81.0% SNO-5, 14.3% SNO-20, 4.8% 55 Pale Oil__________________________________________________________________________Filtered)SNO-10 28.51 4.87 102*amyl 0.16methylbenzyl 0.15 27.99 4.76 100*butyl 0.16methylbenzyl 0.15 28.10 4.82 101*oleyl 0.16methylbenzyl 0.15 28.20 4.81 100*phenyl 0.16methylbenzyl 0.15 28.43 4.79 94*stearyl 0.16methylbenzyl 0.15 28.29 4.79 97In Dewaxed WD-20 containing 4.8% 55 Pale Oil Filtered__________________________________________________________________________DW-WD-20 143.48 10.92 53isooctyl 0.16 isobutyl 0.15 150.90 11.18 51isooctyl 0.16methylbenzyl 0.15 148.78 11.10 51__________________________________________________________________________ *Adduct formed in 55 Pale Oil Filtered concentrate containing 3 weight percent phosphate and heated to 225.degree.F. N. B. Where check viscosity analyses are not indicated, satisfactory chec values were obtained.

The adducts of the invention are compatible with conventional lubricating oil additives including anti-oxidants corrosion inhibitors, foam suppressants and the like. Being entirely organic the adducts are suitable in ashless or low metal formulations. They are effective to improve viscosity index at extremely low dosages. Thus, a base stock showed a VI improvement of 55 to 79 with only 590 parts per million of the adducts.

The oil component of this composition can be any mineral oil compatible with carrying out lubricating functions in the various locations where metal to metal contact occurs in the art. The viscosity ranges of the oil of the above composition may vary widely.

The specific viscosity would naturally depend upon the service for which the composition is designed.

The level of these various components in the oil will depend upon the resultant properties desired.

Claims

1. A lubricating composition comprising a major amount of a mineral lubricating oil and a minor viscosity index improving amount of an adduct of an amine selected from the group consisting of cyclohexyl piperidine, furfuryl amine and amines of the formula: ##EQU2## wherein the substituents are either hydrogen, alkyl or aryl groups having up to 30 carbon atoms with ethyl oleyl acid orthophosphate, the adduct being formed at a temperature of above about 200.degree.F and wherein the amine is present in about a stoichiometric quantity.

2. The composition of, claim 1 wherein said adduct is ethyl oleyl acid orthophosphate-.alpha.-methylbenzyl amine.

3. The composition of, claim 1 wherein said adduct is ethyl oleyl acid orthophosphate-N-cyclohexyl piperidine.

4. The composition of, claim 1 wherein said adduct is ethyl oleyl acid orthophosphate-furfuryl amine.

5. The composition of, claim 1 wherein said adduct is ethyl oleyl acid orthophosphate-isobutyl amine.