US3198738A

US3198738A - Lubricating compositions and additives therefor

Info

Publication number: US3198738A
Application number: US98008A
Authority: US
Inventors: Adriaan H Wagenaar; Krukziener Maurits
Original assignee: Shell Oil Co
Current assignee: Shell USA Inc
Priority date: 1960-07-27
Filing date: 1961-03-24
Publication date: 1965-08-03
Anticipated expiration: 1982-08-03
Also published as: GB934385A; BE606502A; NL106079C; DE1274777B; NL254244A

Description

United States Patent 9 3,11%8138 LUERZQATENQ CGMPGSH'ZEQNd AND ADDETEVES THEE EFfiR Adriaan Wagenaar Maurits Kruhziener, Amsterdam, Netherlands, assignors to Shell Gil ijompany, New Yorlr, N.Y., a corporation of Delaware No Drawing. Filed Mar. 24, 1961, Ser. No. 98,003 Claims priori application Netherlands, July 27, 1960, 254,244 Qlaims. (til. 252-515) This invention relates to improved lubricating oil composition and to oil-soluble additives therefor having improved detergent and wear-inhibiting properties.

Combustion engines, such as gasoline engines and diesel engines, are more or less subject to wear of cylinders, pistons and piston rings. In automobile engines, in particular, it is a known phenomenon that considerably increased wear occurs when the cylinder temperature remains relatively low, as is the case when driving short distances. According to the general view this is due to moisture condensing on the cool cylinder walls in the presence of acids, such as sulfuric acid from sulfurous fuel, hydrochloric acids from lead scavengers, and organic acids from incompletely burnt gasoline. The corrosion caused by these acids, also termed cold corrosion, is responsible for much of the piston and cylinder wear in automobiles.

In order to inhibit wear in combustion engines, it has already been proposed to incorporate in the lubricating oil certain additives capable of rendering the said acids harmless by neutralizing them. Examples are oil-soluble neutral or basic organic metal compounds, such as calcium, barium or zinc salts of petroleum sulfonic acids, of alkylated hydroxy benzoic acids, of dialliyl dithiophosphoric acid and others. In many cases it has been possible to obtain good results by incorporatin such organic metal salts in the lubricating oil. The use of metal salts, however, is attended by drawbacks. One disadvantage, for example, is the fact that the metal salts formed by neutralization of the acids resulting from the combustion are generally insoluble in oil. This may lead to disturbances, particularly as a result of the formation of deposits in the combustion space which may subsequently cause precombustion. I

It has now been discovered that excellent multi-functioual lubricants are provided by incorporating in small amounts an oil-soluble polymeric compound having essentaflly a long linear hydrocarbon backbone chain and attached thereto in a uniform or random fashion two essential groups, (I) one being oximino groups C=N-OH) and (Ii) the other being an oleophilic hydrocarbyl radical of at least 8 and up to 30 or more carbon atoms. The two radicals may be attached directly or indirectly to the hydrocarbon backbone chain. Thus the oximino groups.

may be bound to the backbone chain either directly or through a hydrocarbon group such as a methylene group or benzene group and the oleophilic group may be a hydrocarbon chain (R) of 83() carbon atoms attached directly to the backbone chain, e.g., C1248 straight or branched chain alkyl radical or indirectly through a polar group such as -GR groups, wherein R is as defined. Polymeric compounds of this type should have at least 150 carbon atoms in the backbone chain and a plurality of units (1) and (ii) as described such that the molecular weight of the polymer ranges from about 5,000 to about 1,000,000, preferably from about 50,000 to 500,000.

The invention also relates to a process for the producticn of polymers of the present invention by copolymerizing a polymerizable compound containing at least one carbonyl group C=O) or a polar-containing polymerizable compound capable of being converted to carbonyl groups with a polymerizable compound containing a hydrocarbyl group of at least 8 carbon atoms and treating (oximizinr or oximating) said copolymer with a hydroxyl amine, preferably in a neutral or basic medium of a pH of 710, preferably 7-8, so as to convert the carbonyl groups to orimino groups. Thus, the intermediate portion of the copolymers of this invention may be obtained by copolymerization of a monomer containing a carbonyl group with a monomer containing an oleophilic group having at least 8 carbon atoms, or a copolymer obtained indirectly from these monomers, for example by reducing ester groups to aldehyde groups of a polymer or copolymer containing ester groups, or for example by oxidation of secondary alcohol groups present in a polymer or copolymer to ketone groups. Also copolymers containing acetal groups and the oleophilic hydrocarbyl groups may be converted into carbonyl groups by treat ment with mineral acid.

Examples of monomers of which the copolymers containing aldehyde groups may be composed are unsaturated aliphatic aldehydes. Preference is given to copolmers compound of acrolein or methacrolein and one or more monomers, or copolymers composed of a beta-formalitcrylic acid ester, maleic di-aldehyde or fumaric (ii-aldehyde, and one or more monomers containing the oleophilic groups.

'or straight carbon chain, in particular alpha-olefins having at least 10 carbon atoms, or esters of unsaturated organic monoand dicarboxylic acids and saturated alcohols, or esters of saturated organic carboxylic acids and unsaturated alcohols, which esters contain a saturated branched or straight carbon chain having at least 8 carbon atoms, or unsaturated aliphatic ethers having a saturated branched or unbranched carbon chain containing at least 8 carbon atoms. If desired, mixtures or these monomers may be used, for example a mixture of stearyl methacrylate and lauryl methacrylate. Of the esters of unsaturated monoand dicarboxylic acids and saturated alcohols esters of methacrylic acid are preferred, in particular methacrylic acid esters of which the ester group contains 1248 carbon atoms. The esters of maleic acid and furnaric acid of which at least one of the ester groups contains at least 8 carbon atoms are also suitable for use.

Of the unsaturated aliphatic ethers preference is given to vinyl-allryl ethers in which the alkyl group contains l218 carbon atoms.

The copolymerization of one or more (I) monomers with one'or more (ll) monomers may be carried out in any known manner. Copolymerization may, for example, be carried out by dissolving the monomers in a solvent, such as benzene, or in a mixture of solvents, such as a mixture of benzene and ethanol. A telomerization agent, such as nitrobenzene, may also be added to the solution of the monomers. The copolymerization may be initiated, for example by a thermal treatment or by the addition, possibly at elevated temperature, of an initiator such as dibenzoyl peroxide, azo-bis-isobutyronitrile or other radical-yielding sources. When an initiator is used the optimum copolymerization temperature depends on the rate at which the initiator decomposes. If the reactivity of the monomers is so divergent that the monomer ratio in the copolymer differs considerably from the ratio in which the monomers are brought together before copolymerization, one of the monomers may be added in portions, thereby ensuring the formation of the copolymer having a homogeneous composition.

The following examples illustrate the preparation of polymers of the present invention.

EXAMPLE I 253.5 parts by weight of stearyl methacrylate, 507 parts by weight of benzene and 2 parts by weight of benzoyl peroxide were introduced in a 2-liter three-necked flask provided with a drop funnel, reflux cooler and gas inlet tube. Nitrogen was then passed into the flask for one hour with stirring, after which 84 parts by weight of acrolein were added. The mixture was brought to a temperature of 80 C. by means of a heating bath. After the mixture had been stirred at this temperature for one hour one part by weight of benzoyl peroxide was added, followed by 0.375 part by weight of benzoyl peroxide, after which the mixture was stirred for 18 hours at 80 C. The total reaction time during which the mixture was continuously stirred and nitrogen was passed into the fiask was 24 hours. After cooling the reaction mixture was poured out into 1600 partsby weight of methanol and the acrolein/stearyl methacrylate copolymer which separated was taken up in 500 parts by weight of benzene. This solution was poured out into 1600 parts by weight of methanol and the copolymer was separated washed with methanol. The copolymer was then taken up in benzene and the copolymer isolated by freeze drying from the resultant solution. The yield was 205.8 parts by weight of copolymer, i.e. 61% by weight based on the total quantity of starting monomers. The ratio of the component acrolein and stearyl methacrylate monomers in the copolymer Was 1.27:1. The molecular weight, determined by the light scattering technique, was 98,000.

The copolymer was converted by reaction with hydroxyl amine into a copolymer having oximino groups.

139 parts by weight of the hydrochloric acid salt of hydroxyl amine were dissolved in 400 parts by weight of methanol. A solution of 115 parts by weight of potassium hydroxide in 200 parts by weight methanol was added to this solution. The potassium chloride which separated was removed by filtration and the filtrate having a pH of 7.5 was added to a solution of 203.7 parts by weight of the copolymer in 800 parts by weight of benzene. The mixture was stirred for 18 hours at room temperature and then boiled under reflux for 4 hours with continuous stirring. After the reaction mixture had been concentrated by solvent evaporation to a volume of approximately 700 parts by volume it was poured out into 1600 parts by weight of methanol. The copolymer which separated was washed with methanol, dissolved in 500 parts by weight of benzene and poured out into 1600 parts by weight of methanol. The copolymer which separated was washed with methanol, then dissolved in 500 parts by weight of benzene, after which the resultant solution was filtered. The product was isolated from the filtrate by freeze drying. A quantity of 188.9 parts by weight of the copolymer containing oximino groups was obtained. Analysis showed that the ratio of the component acrolein, acrolein oxime and stearyl methacrylate monomers in this copolymer was 0.4:0.88:1.

EXAMPLE II Acrolein and stearyl methacrylate were copolymerized in the presence of methanol and the copolymerization was carried out as follows:

' A quantity of 1.5 parts by weight of benzoyl peroxide was added at a temperature of 80 C. and with stirring to a mixture of 84 parts by weight of acrolein, 338 parts by weight of stearyl methacrylate, 96 parts by weight of methanol and 633 parts by weight of benzene which was present in a nitrogen atmosphere. After 6, 22 and 28 hours further quantities of 1.0 part by weight, 1.0 part by weight and 0.72 part by weight of benzoyl peroxide respectively were added. The total reaction time was 48 hours, the temperature continuously maintained at C. and nitrogen introduced through a gas inlet tube. After being cooled the reaction mixture was poured out into 2000 parts by weight of methanol and the copolymer separated was washed with methanol.

The resultant copolymer contained acetal groups which were split off by hydrolysis under the influence of hydrochloric acid in the following manner.

The copolymer was dissolved in 600 parts by weight of benzene and the solution mixed with 25 parts by volume of hydrochloric acid or" 38% concentration, and 20 parts by weight of methanol. The mixture was boiled under reflux for 15 minutes and, after being cooled, subsequently poured out into 1600 parts by weight of methanol. The copolymer which separated was washed with methanol, dissolved in 500 parts by weight of benzene and the solution poured out into 1600 parts by weight of methanol. After the resultant copolymer had been washed with methanol it was re-dissolved in benzene and the copolymer was obtained from this solution by freeze drying. The yield was 256 parts by weight, i.e. 60.7 based on the total weight quantity of the monomers.

Analysis showed that the ratio of the components acrolein/dimethyl acetal:acrolein:stearyl methacrylate =4.42:0.22: 1. The molecular weight, determined by the light scattering technique, was 151,000.

The copolymer was converted by reaction with hydroxyl amine into a copolymer containing oximino groups.

146 parts by weight of the hydrochloric acid salt of hydroxy amine was dissolved in 450 parts by weight of methanol. A solution of 48.3 parts by weight of sodium in 200 parts by weight of methanol was added to this solution. After the mixture had been stirred for 2 hours, the resultant sodium chloride was filtered off and subsequently washed with methanol. The filtrate was concentrated by solvent evaporation by means of vacuum distillation at room temperature till the volume was approximately 700 parts by volume.

The solution of hydroxyl amine in methanol of which the pH was 7.2 was added to a solution of 253.5 parts by weight of the copolymer in 800 parts by Weight of benzene. The mixture was boiled under reflux for 5.5 hours. After being cooled it was poured out into 2000 parts by weight of methanol, the product separated was taken up in 500 parts by weight of benzene and the resultant solution poured out into 1600 parts by weight of methanol. The product was then dissolved in 500 parts by weight of benzene and isolated from this solution by freeze drying. The yield was 236 parts by weight, the nitrogen content was 0.77% by weight.

The ratio of acrolein/dimethyl acetalzacrolein oximezstearyl methacrylate in this copolymer was EXAMPLE III Acrolein and stearyl methacrylate were copolymerized under conditions identical to those of Example I, but in this case the benzoyl peroxide was added in two portions, i.e. 0.7 part direct and 0.3 part after 16.5 hours.

The copolymer was isolated in the manner described in Example I. The yield was 56.3%. The monomer ratio of acroleinzstearyl methacrylate in the copolymer Was 0.96:1, the molecular weight, determined by the light scattering technique, was 140,000.

The copolymer was reacted with hydroxyl amine in the manner described in Example II, but the pH of the hydroxyl amine solution was 7.5.

The ratio of acroleinzacrolein oximezstearyl methacrylate in the resultant product=.38:0.57:l, and the nitrogen content was 2.0% by weight.

EXAMPLE 1V Acrolein and stearyl methacryl-ate were copolymerized in benzene as solvent under the conditions of temperature, atmosphere and time as stated in Example I although not all the acrolein was aded direct to the solution of stearyl methacrylate in benzene but was distilled from a distillation flask and passed into the reaction vessel in a period of 5 hours. Half of the quantity of benzoyl peroxide 1% by weight based on the total quantity of the monomers to be copolymerized) was immediately added, after which the other half was gradually added to the reaction mixture over a period of 5 hours.

The starting quantities were 114 parts by weight of acrolein, 338 parts by weight of stearyl methacrylate, 675 parts by weight of benzene and 4.5 parts by weight of benzoyl peroxide.

The reaction product was isolated in the manner described in Example I. The yield was 290 parts by weight, i.e. 64.2%.

Calculated from the data obtained by analysis, the ratio of the acrolein and stearyl methacrylate monomers in the copolymer was 0.80:1 and in the copolymer 24% or" the number of aldehyde groups was present in the hydrate form. The molecular weight, determined by the'light scattering technique, was 162,000.

The conversion into a copolymer having oximino groups by the reaction with hydroxyl amine was carried out in the manner described in Example II. A product containing 2.53% by weight of nitrogen was obtained. The ratio of acroleimacrolein oximezstearyl methacr late in the copolymer was 0.07:0.73zl.

EXAMPLE V By the method similar to the one described in Example TV but in which the acrolein was distilled from a distillation flask and passed into the reaction vessel in a period of 1.25 hours and the benzoyl peroxide was gradually added in a period of 3 hours, a copolymer was obtained in a yield of 66.5% of which the monomer composition of acrolein:acrolein hydrate:stearyl methacrylate was 1.11:0.2221. The molecular weight, determined by the light scattering technique, was 90,000.

This copolymer was converted with hydroxyl amine obtained from the hydrochloric acid of hydroxyl amine and pyridine.

90 parts by weight of pyridine were added to a solution of 69.5 parts by weight of the hydrochloric acid salt of hydroxyl amine in 160 parts by'weight of methanol of 70% concentration. A solution of 210 parts by weight of the copolymer and 500 parts of benzene was added to this mixture of which the pH was 6.7 and the resultant mixture was stirred at room temperature for 2 hours and then stirred and boiled under reflux for 3 hours. The copolyrner was isolated from the cooled reaction mixture in the manner described in Example I. The yield was 206 parts by weight, the nitrogen content was 1.71% by weight. The monomer ratio of acroleinzacrolein oximezstearyl methacrylate in the copolymer was 0.61:0.5 0:1.

EXAMPLE VI 98 parts by weight of acrolein diethylacetal and 5.0.7 parts by weight of stearyl methacrylate were dissolved in 120 parts by weight of benzene. A quantity of 0.5 part by weight of azo-bis-isobutyronitrile was added to this solution. The temperature of the solution was brought to 65 C. and the solution was kept at this temperature for 50 hours with stirring. After 21 and after 29 hours respective quantities of 0.25 parts by weight of azo-bisisobutyro nitriel were added. A nitrogen atmosphere was maintained during the reaction in the reaction vessel. The resultant copolymer was isolated as described in the previous examples. The yield was 51 parts by weight, i.e. 3.3%

51 parts by weight of copolymer of acrolein-diethyl acetal and stearyl methacrylate were dissolved in 500 parts by weight of benzene. After the addition of 75 parts by volume of concentrated hydrochloric acid and 60 parts by weight of ethanol the mixture was boiled under reflux for 1 hour. When it was cooled the reaction mixture separated into two layers. The bottom layer was removed and the top layer washed with water and with a dilute sodium bicarbonate solution, after which the washed solution was transierred to a reaction vessel.

After the addition of a solution of 70 parts by weight of hydrochloric acid salt of hydroxyl amine and 60 parts by weight of potassium hydroxide in 1500 parts by weight of ethanol of 50% concentration the mixture was stirred at room temperature for 20 hours. After the aqueous layer had been separated the filtrate was concentrated by solvent evaporation and the resultant reaction product isolated by pouring out the mixture in methanol and washing it with methanol as described in the previous examples. The result was 47 parts by weight, the nitrogen content was 0.47% by weight. The monomer ratio of acrolein, acrolein oxirne and stearyl methacrylate in t copolyrner was 0. 007:0.13:1.

EXAMPLE VII 416 parts by weight of stearyl methacrylate and 106 parts by weight of methyl isopropenyl ketone were dissolved in 2088 parts by'weight of benzene. After the addition of 5.8 parts by weight of benzoyl peroxide the temperature was raised to C. and the mixture was kept at this temperature for 48 hours with stirring, refluxing of the evaporating solvent being ensured. After 6 hours 93 parts by weight of stearyl methacrylate were added as well as 5.8 parts by weight of benzoyl peroxide. After 32 hours 5.8 parts by weight of benzoyl peroxide were again added.

The product was isolated by pouring out the mixture into methanol, taking up the copolymer which separated into benzene, by again pouring out the solution into methanol as described in the previous examples. The yield was 448 parts by weight of stearyl methacrylate/ methyl isopropenyl ketone copolymer. The ratio of the methyl isopropenyl ketone and stearyl methacrylate monomers in the copolymer was 0.137z1.

224 parts by weight of the resultant copolyrner were dissolved in 725 partsby weight of benzene. A solution of 24.75 parts by weight of hydroxylamine in 250 parts by weight of methanol obtained from the hydrochloric acid salt of hydroxyl amine and sodium methylate as described in Example 11, was added to this solution. The mixture was boiled under reflux and stirred for 5.5 hours. The reaction product was isolated by pouring out the reaction mixture in methanol as described in the previous examples.

The nitrogen of the resultant product was 0.56 part by weight. The ratio of the methyl isopropenyl ketone oxime and stearyl methacrylate monomers in the copolymer was 0.87:1. The yield was 225 parts by weight.

When desired, additional improvements with respect to oxidation stability and scufiing inhibition can be imparted to the oil compositions containing the copolymers of this invention by incorporating small amounts (0.01- 2%, preferably 0.11%) of phenolic antioxidants such as alkylphenol, e.g., 2,6-ditert.butyl-4-methyl phenol or p,p'-rnethylene bisphenols such as 4,4'-methylene (2,6- ditert.butyl phenol) or arylarnines such as phenyl-alphanaphthylamine and mixtures thereof. Anti-scufling agents include organic phosphites, phosphates, phosphonates and their thio-derivatives, such as C alltyl phosphites, or phosphonates, e.g., diand tributyl, octyl, lauryl, stea1yl, cyclohexyl, benzyl, cresyl, phenyl, phosphites or phosphates, as well as their thio-den'vatives, P S -terpene reaction products, e.g., P S -pine oil reaction product and alkali metal salts thereof such as potassium salt of a P S -terpene reaction product, phosphonates such as dibutyl methanephosphonate, dibutyl trichloromethanephosphonate, dibutyl monochlorornethanephosphonate, dibutyl chlorobenzenephosphonate, and the like. The full esters of pentavalent phosphorus acids such as triphenyl, tricresyl, trilauryl and tristearyl ortho phosphates or potassium salt of P S -terpene reaction product are preferred.

The oximino-containing polymeric additives of this invention improve various petroleum or synthetic products by the incorporation of a minor amount (0.001% to 10%, preferably 0.1% to 5% by Weight) of the additive. Thus, they may be used to improve gasoline, jet fuels, transformer oils, turbine oils, mineral lubricating oils, synthetic lubricating oils, e.g., polyolefins, esters of dibasic acid, silicone polymers, etc., industrial oils such as hydraulic fluids, metal working fluids and quenching fluids. The oximino-containing polymers are particularly useful in refined mineral lubricating oils, which may range from SAE 5W viscosity grade to SAE 140 grade and which may be derived from parafiinic, naphthenic or asphaltic base crudes. Representative oils are refined high viscosity index mineral oils having a viscosity of 100 F. of 100 to 250 SUS. A typical mineral lubricating oil (X) of this type is an extracted Venezuelan paraffinic lubricating oil having a viscosity of 114 cs. at 100 F. and a California mineral lubricating oil (Y) may have the following properties:

Gr., API, 60/60 F 32 Flash, F. 370 Viscosity index (Dean and Davis) 93 Viscosity, SUS at 100 F. 103

The copolymers according to the invention may be added as such to lubricating oils. In an advantageous embodiment the product is only partly freed from the solvent, for example by steam distillation, after Which a small quantity of a lubricating oil is added and the remainder of the solvents is finally distilled off by means of steam, preferably under reduced pressure. The resultant concentrate can then be diluted with a lubricating oil.

The following non-ash compositions are representative of this invention:

Composition A Example I copolymer 2% wt. Mineral lubricating oil (X) Balance.

Composition B Example II copolymer 2% wt. Mineral lubricating oil (X) Balance.

Composition C Example III copolymer 2% wt. Mineral lubricating oil (X) Balance.

Composition D Example 1V copolymer 2% wt. Mineral lubricating oil (X) Balance.

Composition E Example V copolymer 2% wt. Mineral lubricating oil (X) Balance.

Composition F Example I copolynier 2% wt. 4,4-methylene bis(2,6-ditert. butyl phenol) 0.75% wt. Mineral lubricating oil (X) Balance.

Composition G Example I copolyiner wt. 4,4-methylene bis(2,6-ditert. butyl phenol) 0.5% wt. T ricresyl phosphate 0.8 wt. Mineral lubricating oil (X Balance.

To illustrate the superior and unexpected results obtained with compositions of the present invention the following compositions shown in Table I were engine tested in a (1) Caterpillar diesel engine, (2) Gardner diesel engine, (3) Petter gasoline engine and in (4) a C.F.R. gasoline engine and the results were as follows:

TABLE I High Low Re- Temp. Temp. duction Composition Piston Piston Condi- Condiin Piston Fouling Fouling tion tion Ring Rating Rating Piston Sludge Wear (10: Fouling Rating Comperfect) perfect) Rating (1 pared to (10= clean) Neat clean) Oil Mineral lubrieating oil (X) Mineral lubricating oil (X) +15% 4,4- methylene bis(2.6-ditcrt. butyl phenol) a Engine test conditions.

Caterpillar Diesel Engine Water-cooled, single-cylinder, four-stroke engine. The test lasted 48 hours. The fuel was a gas oil having a sulfur content of 0.9% by Weight. The cooling Water temperature was about 80 C. The engine power was 18 H.P., bore 146 mm., stroke 203.2 mm., swept volume 3.4 liters.

Gardner Diesel Engine Water-coled, single-cylinder, four-stroke engine. The test lasted 17 hours. The fuel was a gas oil having a sulfur content of 0.9% by weight. The cooling water temperature was about 80 C. The engine power was 11 H.P., bore 108 mm., stroke 152.4 mm., swept volume 1.4 liters.

C.F.R. Gasoline Engine Water-cooled, single-cylinder, four-stroke engine, bore 83.85 mm., stroke 114.3 mm., swept volume 628 cu. cm. The test lasted hours. The fuel was a gasoline having a sulfur content of 0.05% by weight and contained 1.2 ml. TEL per U.S. gallon. The cylinder cooling watertemperature was approximately 40 C.

Petter Gasoline Engine, No. 1

Water-cooled, single-cylinder, four-stroke engine, bore 85 mm., stroke 82.5 mm., swept volume 468 cu. cm. The test lasted 28 hours. The fuel was a motor gasoline having 1.2 ml. TEL per U.S. gallon and a sulfur content of 0.05% by weight. The cylinder cooling water temperature was approximately C. The temperature of the cooling water of the cooled valve cover was approximately 20 C.

Fetter Gasoline Engine No. 2

Cooled single-cylinder, four-stroke engine, bore mm., stroke 82.5 mm., swept volume 368 cu. cm. The

test lasted 48 hours. The fuel was a motor gasoline having 1.2 ml. TEL per US. gallon and a sulfur content of 0.05% by Weight. The cooling liquid temperature was approximately 160 C.

Lubricating compositions of this invention are particularly applicable for high temperature, high speed use as in aviation engines, automotive engines, truck engines as well as industrial equipment.

We claim our invention:

1. An improved mineral lubricating oil composition comprising a major amount of mineral lubricating oil and from 0.1% to by weight of an oil-soluble polyoximino-containing copolymer obtained by polymerizing at reflux temperature and in the presence of a free radical initiator a polymerizable unsaturated carbonyl containing compound selected from the group consisting of a low molecular Weight olefinic ketone and a low molecular weight olefinic aldehyde and C1248 alkyl methacrylate in the mol ratio of from about 0.1:1 to about 220.1, respectively, and reacting said copolymer with hydroxylamine at a pH of 7-10, to etiect conversion of the carbonyl groups to oximino groups, said copolymer having a molecular Weight of from 50,000 to 1,000,000.

2. An improved mineral lubricating oil composition comprising a major amount of mineral lubricating oil and from 0.1% to 10% by weight of an oil-soluble polyoximino-containing copolymer obtained by polymerizing at reflux temperature and in the presence of benzoyl peroxide catalyst acrolein and C alkyl methacrylate in the mol ratio of from about 0.111 to about 2:01, respectively and reacting said copolymer with hydroxyl amine at a pH of 7-8 to effect conversion of the carbonyl groups to oximino groups, said copolymer having a molecular Weight of from 50,000 to 500,000.

3. An improved mineral lubricating oil composition comprising a major amount of mineral lubricating oil and from 0.1% to 10% by weight of an oil-soluble polyoximino-containing copolymer obtained by polymerizing at reflux temperature and in the presence of benzoyl peroxide catalyst acrolein and stearyl methacrylate in the mol ratio of from about 0.1:1 to about 2:0.1, re-

i0 spectively and reacting said copolymer with hydroxyl amine at a pH of 7-8 to effect conversion of the carbonyl groups to oximino groups, said copolymer having a molecular Weight of from 50,000 to 500,000.

4. An improved mineral lubricating oil composition comprising a major amount of mineral lubricating oil and from 0.1% to 10% by weight of an oil-soluble polyoXimino-containing copolymer obtained by polymerizing at reflux temperature and in the presence of azo-bis-isobutyronitrile catalyst acrolein, diethylacetal and stearyl methacrylate in the mol ratio of from about 0.1:1 to about 2:0.1, respectively and reacting said copolymer with hydroxyl amine at a pH of 7-8 to effect conversion of the carbonyl group to oximino groups, said copolymer having a molecular weight of from 50,000 to 500,000.

5. An improved mineral lubricating oil composition comprising a major amount of mineral lubricating oil and from 0.1% to 10% by weight of an oil-soluble polyoXimino-containing copolymer obtained by polymerizing at reflux temperature and in the presence of benzoyl peroxide catalyst methyl isopropenyl ketone, and stearyl methyacrylate in the mol ratio of from about 0.1:1 to about 220.1, respectively and reacting said copolymer with hyd-roxyl amine at a pH of 7-8 to effect conversion of the carbonyl groups to oximino groups, said copolymer having a molecular Weight of from 50,000 to 500,000.

References Cited by the Examiner UNITED STATES PATENTS 2,122,707 7/ 38 Balthis 26063 X 2,800,450 7/57 Bondi et al 252--51.5 2,800,452 7/57 Bondi et al. 25251.5 2,870,129 1/59 Merriam 260-861 2,912,418 11/59 Johnson et a1. 26086.1 2,949,445 8/60 Blake 260-861 2,962,477 11/60 Blanchette 26063 2,984,654 5/61 Agius et al. 252-515 X 2,985,610 5/ 61 Blanchette et al. 26063 X DANIEL E. WYMAN, Primary Ex miner. JULIUS GREENWALD, Examiner.

Claims

1. AN IMPROVED MINERAL LUBRICATING OIL COMPOSITION COMPRISING A MAJOR AMOUNT OF MINERAL LUBRICATING OIL AND FROM 0.1% TO 10% BY WEIGHT OF AN OIL-SOLUBLE POLYOXIMINO-CONTAINING COPOLYMER OBTAINED BY POLYMERIZING AT REFLUX TEMPERATURE AND IN THE PRESENCE OF A FREE RADICAL INITIATOR A POLYMERIZABLE UNSATURATED CARBONYL CONTAINING COMPOUND SELECTED FROM THE GROUP CONSISTING OF A LOW MOLECULAR WEIGHT OLEFINIC KETONE AND A LOW MOLECULAR WEIGHT OLEFINIC ALDEHYDE AND C12-18 ALKYL METHACRYLATE IN THE MOL RATIO OF FROM ABOUT 0:1:1 TO ABOUT 2:0:1, RESPECTIVELY, AND REACTING SAID COPOLYMER WITH HYDROXYLAMINE AT A PH OF 7-10 TO EFFECT CONVERSION OF THE CARBONYL GROUPS TO OXIMO GROUPS, SAID COPOLYMER HAVING A MOLECULAR WEIGHT OF FROM 50,000 TO 1,000,000.