US3247113A

US3247113A - Lubricating compositions and additives therefor

Info

Publication number: US3247113A
Application number: US205231A
Authority: US
Inventors: Hasserodt Ulrich; Kurt H G Pilgram; Friedrich W A G K Korte
Original assignee: Shell Oil Co
Current assignee: Shell USA Inc
Priority date: 1961-11-13
Filing date: 1962-06-26
Publication date: 1966-04-19
Anticipated expiration: 1983-04-19
Also published as: US3318915A

Description

United States Patent Ofiiice 3,247,113 Patented Apr. 19, 1966 4 Claims. (cl. zsz 49.s

-The present invention relates to improved lubricants and more particularly to liquid and solid lubricating compositions possessing superior adhesive, anti-oxidant and corrosion inhibiting properties.

It is generally known that lubricating compositions tend to oxidize in service and to form corrosion products, sludge and lacquer. Decomposition of the lubricants by oxidation results in acid products which attack the metal surface. This leads to excessively rapid wear of moving engine parts in particular. The resultant damage necessitates replacement of certain engine parts or even a premature c-omplete overhaul of the machines.

First grade stable lubricating oils which do not corrode per se, for example turbine oils highly refined for special uses, or synthetic lubricants developed for special cases have usually been found to oxidize very readily and to degrade and to have a progressively corrosive eifect even under normal operating conditions.

Now in accordance with the present invention excellent lubricating compositions are prepared by incorporating into the base lubricant'a small amount (0.001-10%,

preferably 0.015%) of an oil-soluble alpha-hydroxy phosphonic acid diesters and may be represented by the formula:

R2 H R1-CP I ll\ OH 0 OR; (I)

wherein R is an organic, substituted or unsubstituted, heterocyclic group containing oxygen, and R and R are hydrocarbyl radicals, at least one of which is a long, aliphatic, branched or unbranched hydrocarbon group, prepared by a novel process of the present invention. The formation of the diesters of the present invention as represented by Formula I is unexpected since it is known that esterification of hydroxy phosphonic acids with higher alcohols generally results in partial or monoesterification as evidenced by reference to Drake and Marvel in the Journal of Organic Chemistry 2 (1937) pages 387-399.

The diesters of the present invention as represented by. Formula I are prepared by the conversion of dialkyl hydrogen phosphites with the corresponding carbonyl compounds, such as aldehydes and ketones, by the catalytic action of basic materials. The basic catalyst is essential since it is possible to heat mixtures of aldehydes and dialkyl hydrogen phosphites without any perceptible reaction taking place. If, however, a small quantity of basic material is present, such as sodium ethyl-ate or triethylamine, the reaction starts instantaneously with evolution of heat with the formation of alpha-hydroxymethyl phosphonic acid diesters. For instance, the reaction between dimer acrolein and dialkyl phosphite in which 2-(2,3-dihydro-gamma-pyranyl) alpha-hydroxymethyl phosphonic acid dialkyl ester is formed proceeds as follows:

The formation of Z-furyl-alpha-hydroxymethyl phosphonic acid dialkyl ester from furfural and dialkyl hydrogen phosphite proceeds in the same way:

The symbols R and R in compounds represented by II and III are the same as in Formula I and specifically at least one unbranched hydrocarbon group. Compounds in which at least one of the R or R groups has at least 6 and preferably up to 16 carbon atoms effect a particularly good inprovement in the adhesion and thus prevent the oxidation of mineral oil-based lubricants or lubricating greases. Good results are also obtained when the compounds according to the invention contain an R or R group having more than 16 carbon atoms.

The following are illustrative examples of substituted alpha-hydrox'y phosphonic acid diesters which may be used according to the invention: 2-(2,3-dihydro-gamrnapyranyl) alpha-hydrOxymethyl phosphonic acid-di-n-alkyl esters, in which the alkyl groups are n-amyl-, n-octyl-, n-dodecyl, n-tetradecyl-, n-hexadecyl groups; 2-furylalpha-hydroxymethyl phosphonic acid-di-n-alkyl esters,

in which the alkyl groups are n-octyl-, n-dodecyl-, ntetradecyl-, n-hexadecyl groups; and also 2-(2,3-dihydrogamma-pyranyl) alpha-hydroxymethyl phosphonic acidethyl-m-hexyl esters and 2-furyl-alpha-hydroxyrnetl1yl phosphonic acid ethyl-n-hexyl esters.

The dialkyl hydrogen phosphites required for the preparation of alpha-hydroxymethyl phosphonic acid dialkyl esters are prepared by reacting phosphorus trichloride (1 mole) with the corresponding alcohol (3 moles) in the presence of a tertiary amine such as pyridine (Py) (2 moles), accordingto the following reaction scheme:

In this way it was possible for the first time to prepare extremely pure, long'chain dialkyl phosphites, e.g. in R=nC H nC H I1C15H33 consequently represent new compounds.

According to the above process it is only possible to prepare symmetric dialkyl hydrogen phosphites. Asymmetric diaikyl hydrogen phosphites, in particular those having at least one long-chain alkyl group, are produced 3 in a novel way by reacting an alcohol with phosphorous acid ester dichloride in the presence of a tertiary amine, such as pyridine, according to the following reaction scheme:

R OPClz P 211 011 moron; Py-I-IC1 R301 Thus, a 79% yield of the compound ethyl-n-hexyl hydrogenphosphite not yet described in the literature was obtained by reacting ethanol (2 moles) with the mixture of n.C H OPCl (1 mole) and pyridine (1 mole) in petroleum ether at C.

The likewise novel compound ethyl-n-octyl hydrogen phosphite was obtained in the same way.

The novel alpha-hydroxymethyl phosphonic acid diesters are partly difficultly distillable liquids and partly crystalline materials which are either odorless or have slight but agreeable odor. They are readily soluble in oil and have no irritating effect on the skin.

The following examples specifically illustrate the additives of the present invention.

Example I.-2-(2.3-dilzydro-gamma-pyranyI) alpha-hydroxymethyl phosphonic acid-di-n-amyl ester vA quantity of 103 g. (0.93 mole) of dimer acrolein (2-formyl-2,3-dihydro-alpha-pyran) was mixed with 206 g. (0.93 mole) of di-n-amylphosphite. A sodium ethylate solution was added dropwise with stirring. The first drops should be added with great care as the temperature will rise spontaneously. The reaction mixture was then suitably externally cooled with ice-water to prevent the temperature from exceeding 80 C., and the reaction was stopped by adding additional di-n-amylphosphite to ascertain whether the temperature rose again. When this is no longer the case, the reaction product is neutralized with acetic acid and distilled in vacuo.

B.P. =l22125 C.; n =1.4625; Yield=102 g. (33% of theory) C H O P Calculated P=9.3%; Found Example II.2-(2.3-dihyar0-gamma-pyrtmyl) alpha-hydroxymethyl phosphonic acid-di-n-hexyl ester A quantity of 55 g. (a slight excess) of dimer acrolein was mixed with 100 g. of di-n-hexylphosphite and reacted as in Example I. After neutralizing with acetic acid the mixture was taken up in ether, the ethereal solution washed once with a solution of sodium hydrogen sulfite and subsequently with ice-water and dried over sodium sulfate. After the ether had been distilled off the material was freed from remaining solvent for one hour at 120 C. and a pressure of 0.05 mm. Hg.

Yield 120 g. (83.5% of theory); 11 1.4704.

A sample was distilled in high vacuum:

Example III.-2-(2.3-dihydr0-gwmma-pyranyl) alphahydroxymethyl phosphonic acid-di-n-0ctyl ester A quantity of 60 g. (a slight excess) of dimer acrolein was mixed with 153 g. of di-n-octylphophite and reacted as in Example I. The resultant reaction mixture was worked up as in Example II.

Yield 171.5 g. (80% of theory); n =1.4689. C H O P Calculated P=7.4%; Found=7.61%.

Example 1V.2-(2.3-dihydro-gamma-pyranyl) alpha-hydroxymetlzyl phosphonic acid-di-n-dodecyl ester (a) A quantity of 558 g. (3 moles) of lauryl alcohol was dissolved in 1.5 liters of petroleum ether in a 4-liter three-necked flask provided with a reflux condenser and drying tube, stirrer and dropping funnel. A quantity of 158 g. (2 moles) of pyridine was added and the mixture cooled to 0 C. with stirring. A quantity of 137.5 g.

1st fraction: B.P. 140-145 C.; 190 g. (93% of theory) of dodecyl chloride.

2nd fraction: B.P. 193195 C.; 140 g. (33% of theory), n 1.4472, M.P.: C.

C H P Calculated P=7.42%; Found P=7.02%.

(b) A quantity of 24 g. (1.6 g. excess) of dimer acrolein was mixed with 83.6 g. (0.2 mole) of di-n-dodecyl phosphite prepared according to (a) and reacted as in Example I. The reaction mixture was worked up as in Example II.

Yield 87 g. (82% of theory); n =1.4700.

After some time the ester turned crystalline and could be recrystallized from ether. M.P.=39.540.5 C.

G l- 0 1 Calculated P=5.83%; Found P=5.27%.

. Example V.-2-(2.3-dihydro-gamma-pyranyl) alpha-hydroxymethyl plies-phonic acid-di-n-tetradecyl ester (21) A quantity of 160.5 g. (0.75 mole) of tetradecyl alcohol was dissolved in 600 ml. of petroleum ether in a 2-liter three-necked flask, a quantity of 39.5 g. (0.5 mole) of pyridine being subsequently added. The flask was provided with a reflux condenser and drying tube and a quantity of 34.4 g. (0.25 mole) of phosphorus trichlo ride was added dropwise with ice-cooling and stirring. After all the trichloride had been added the mixture was heated on a water bath to its boiling temperature for 4 hours with stirring, and after cooling the mixture the pyridinium chloride was removed by suction, after which the precipitate was thoroughly washed with petroleum ether. The petroleum ether was combined with the filtrate and the solvent subsequently removed on a Water bath, the di-n-tetradecyl phosphite residue being subjected to distillation in vacuo.

1st fraction: B.P. mm): 0; Yield: 42 g. (72.5%

of theory) of myristyl chloride.

2nd fraction: B.P. mm): ISO-230 C., 10 g., intermediate fraction.

3rd fraction: B.P. 230 C.; Yield: 95 g. (78% of theory).

M.P.: 39-40 C.; solidification point: 28 C.

C H O P Calculated P=6.55%; Found P=6.05%.

(b) A quantity of 3.5 g. of dimer acrolein was mixed with 14.4 g. of di-n-tetradecyl phosphite prepared according to (a) and reacted as in Example I. The reaction mixture was worked up as in Example II and the crude product recrystallized from methanol.

Yield: 7.5 g. (34% of theory); M.P. 5152 C. C34H67O5P Calculated P=5.28%; Found P=5.25%.

Example VI.2-(2;3-dihydro-gamma-pyranyl) alpha-hydroxymethyl phosphonic acid-di-n-lzexadecyl ester (a) A quantity of 181.5 g. (0.75 mole) of cetyl alcohol was dissolved in 600 ml. petroleum ether in a 2-liter three-necked flask, 39.5 g. (0.5 mole) of pyridine being subsequently added. A quantity of 34.4 g. (0.25 mole)! of phosphorus trichloride was slowly added dropwise at 0 C. with stirring and cooling, the mixture then being heated to its boiling temperature for 4 hours while refluxing it. After cooling the mixture the pyridinium chloride was removed by suction after which the precipitate was washed with petroleum ether, the petroleum ether was removed on a water bath with a reflux condenser and the flask residue containing di-n-hexadecyl phosphite distilled in vacuo.

1st fraction: B.P. 135 C.; Yield: 48 g. (74% of theory) of cetyl chloride.

2nd fraction: B.P. mm): 180-245 C., g., intermediate fraction.

3rd fraction: B.P. 245.250 C.; Yield: 100 g.

(75.5% of theory).

M.P.: 46-47 C.; Solidification point: 34.5 C.

C H O P Calculated P=5.85%; Found P=5.78%.

(b) A quantity of 3.19 g. of dimer acrolein was mixed with 15 g. of di-n-hexadecyl phosphite prepared according to (a) and reacted as in Example I. The reaction mixture was worked up as in Example II and the crude product recrystallized from methanol.

Yield: 6.5 g. (36 %of theory); M.P. 48 C. C H O P Calculated P=4.83%; Found P=5.18%.

Example VII.-2-furyl-alpha-hydroxymethyl phosphonic acid-di-n-octyl ester A quantity of 9.6 g. (0.1 mole) of furfural together with 30.6 g. (0.1 mole) of di-n-octyl phosphite were heated to 80 C. in an oil bath. 1 ml. of triethylamine was then added dropwise, whereupon the reaction solution heated to 85 C. The solution was left to stand at 80 C. for a further 4 hours. The reaction product was Washed with a solution of sodium hydrogen sulphite and subsequently with water, taken up in ether and dried over sodium sulfate. After removal of the ether, finally at 100 C. and under a pressure of 0.5 mm. Hg, a yellow oil remained behind.

Yield: 35.5 g. (89% of theory); n =1.4617. C H O P Calculated P=7.7%; Found P=7.9%.

Example VIIL-Z-furyl-alpha-hydroxymethyl phosphonic acid'di-n-dodecyl ester A quantity of 4.8 g. (0.05 mole) of furfural and 20.9 g. (0.05 mole) of di-n-dodecyl phosphite prepared as in Example IVa were reacted as in Example VII. After working up, a yellow oil remained behind.

Yield: 21 g. (82% of theory); n =l.4682. C H O P Calculated P=6.03%; Found P=6.25%.

Example IX.2-furyl-alpha-hydroxymethyl phosphonic acid-di-n-tetradecyl ester A quantity of 4.8 g. (0.05 mole) of furfnral together with 23.7 g. (0.05 mole) of di-n-tetradecyl phosphite prepared as in Example Va were heated at 80 C. in an oil bath. A quantity of 1.5 ml. of triethylamine was subsequently added dropwise, whereupon the reaction solution heated to 85 C. The solution was left to stand at 80 C. for a further 4 hours. A yellow oil was obtained which was freed from triethylamine and unconverted starting materials at 100 C. under a pressure of 0.01 mm. Hg. After cooling the product a bright yellow mass of waxy consistency which melted between C. and 25 C. remained behind.

Yield: 27 g. (95% of theory). C H O P Calculated P=5.43%; Found P=5.5%.

Example X.2-furyl-alpha-hydroxymethyl phosphonic acid-di-n-hexadecyl ester A quantity of 4.8 g. (0.05 mole) of furfural together with 26.5 g. (0.05 mole) of di-n-hexadecyl phosphite prepared as in Example Via were reacted as in Example VII. After working up the solution as in the previous example a yellow waxy reaction product remained behind, which could not be recrystallized from methanol or petroleum ether.

Yield: 30.5 g. (97.5% of" theory); M.P.=20 C. C37Hq1O5P Calculated P=4.95%; Found P=4.79%.

Example XI.-2-(2.3-dihydro-gamma-pyranyl) alphahydroxy'methyl phosphonic acid ethyl-n-hexyleszer (a) A quantity of 500 ml. of petroleum ether and 185 g. of n-hexoxydichlorophosphine (C H OPCI were put in a 2-liter three-necked flask provided with a reflux condenser and drying tube, stirrer and dropping funnel. A mixture of 84 g. of ethanol and 72 g. of pyridine was then carefully added dropwise with ice-cooling and stirring. After completion of the addition the product was stirred for 2 hours at room temperature, freed from pyridinium chloride by suction and, after the petroleum ether had been removed in vacuo, distilled through a 20 cm. vacuum-jacketed column.

1st fraction: (diethyl phosphite) B.P. 6268 C.

2nd fraction: (ethyl -n -hexyl hydrogen phosphite) B.P. 118120 C.; Yield: 140 g. (79% of theory); r1 1.4249.

C H O P Calculated P: 15.97%; Found P=15.9%.

(b) A quantity of 11.2 g. (0.1 mole) of dimer acrolein and 19.4 g. (0.1 mole) of ethyl-n-hexyl hydrogen phosphite prepared according to (a) were introduced into a ml. flask provided with reflux condenser, stirrer and dropping funnel. A quantity of 1 ml. of triethyl amine was slowly added dropwise at 20 C. with stirring, the inside temperature rising to 73 C. The reaction product turned reddish brown and was left to stand at 70 C. for a further 3 hours. After being cooled and taken up in ether the product was washed with 20 ml. of sodium hydrogen sulfite solution and then with ice water, and subsequently dried over sodium sulfate. The ether was removed by distillation and the remaining unconverted esters were finally removed at 100 C. and a pressure of 0.05 mm. Hg. A reddish-yellow, bright oil remained behind.

Yield: 30.2 g. (98.5% of theory); 12 1.4700. C I-1 0 1 Calculated P=10.13%; Found P:9.95%.

Example XII.2-fmyl-alpha-hydr0xymethyl phosphonic acid etlzyl-n-lzexyl ester A quantity of 9.6 g. (0.1 mole) of furfural and 19.4 g. (0.1 mole) of ethyl-n-hexyl hydrogen phosphite prepared as in Example Xia were reacted as in Example XIb. After working up the mixture a yellow oil with n 1.4735 remained behind.

Yield: 26 g. (89.7% of theory). C H O P Calculated P=10.69%; Found P=10.7%.

Example XIII.-2-(2.S-dihydro-gamma-pyranyl) alphahydroxymethyl phosphonic acid ethyl-n-0ctyl ester (a) A quantity of 222 g. of H-CgH1 QPC12 was slowly added dropwise with stirring and ice cooling to a solution of 88.5 g. of ethanol and 76 g. of pyridine in 600 ml. of

' petroleum ether contained in a 2-liter three-necked flask provided with reflux condenser and drying tube, stirrer and dropping funnel. After completion of the addition stirring was continued at room temperature for 2 hours, the product freed from pyridinium chloride by suction, the petroleum ether then removed on a water bath by distillation and the residue, containing ethyl-n-octylhydrogen phosphite, distilled in vacuo 1st fraction: B.P. mm): 30-60 C. (70 g.); my:

1.4192; P c0ntent=1l.35%.

2nd fraction: B.P. (M2 mm): 9296 C.; n =1.4290;

Yield: 65.0 g. (30.4% of theory).

C H O P Calculated P=13.96% Found P: 14.1%.

(b) A quantity of 5.6 g. of dimer acrolein and a quantity of 11.1 g. of ethyl-n-octylhydrogen phosphite prepared as in (a) were reacted as in Example XIb and worked up. A yellowish, bright oil was obtained.

Yield: 15.4 g. (92% of theory); n =1.4712. C 'H O P Calculated P:9.28%; Found P=9.65%.

A quantity of 4.8 g. of furfural and a quantity of 11.1 g. of ethyl-n-octyl phosphite prepared as in Example XHIQE were reacted as in Example XIb and worked up. A quantity of 15.1 g. (95% of theory) of a yellow oil were obtained.

n =l.4733. C H O P Calculated P=10.4%; Found P=10.2%.

The amount of novel alpha-hydroxymethyl phosphonic acid diesters to be used depends on the particular lubricant to which they are added and on the use of which the lubricant is intended. The lubricant may be used in amounts varying from 0.01 to or more, occasionally it is also possible to use less than 0.01%, for instance 0.001%.

The lubricating materials, which together with the alpha-hydroxymethyl phosphonic acid diesters yield very high-grade lubricants, are neutral fluids which may be hydrocarbons or mixtures of hydrocarbons, for instance any desired mineral lubricating oil. The fluid may be thickened to a grease with a thickening agent. Synthetic oils, such as polymerized olefins or combined polymers of alkylene glycols and alkylene oxides, are also suitable for use as neutral fluid. The lubricants may also be mixtures of synthetic lubricating materials and natural oils. In addition to the alpha-hydroxymethyl phosphonic acid diesters other additives, such as pour point depressants or viscosity improvers, may be admixed with the lubricant.

The following experiments show the superiority of the lubricants according to the invention to the conventional lubricants, in which trialkyl phosphites are admixed as additives. The rust-preventing characteristics of turbine oils were measured in the presence of water according to ASTM standard D665-54. According to this method cylindrical steel specimens are immersed in 300 ml. of the oil under test together with 30 ml. of distilled water, the test being run for 24 hours at a temperature of 60 C. An estimate is then made of the percentage of rusting of the metal surface. (cf. 1958 Book of ASTM Standards Part 7, page 303.) The results are given in the following table.

Compositions of this invention are useful for providing stability and other desired properties to petroleum products such as mineral lubricating oils which also contain small amounts (0.1% to 3%) of other agents such as the following: detergents such as metal organic sulfonates, e.g., neutral or basic Ca, Ba, or Zn petroleum sulfonates or non-ash forming detergents such as Acryloids of the 300 and 900 series, e.g., Acryloid 917, 966 or 315X which are copolymers of vinyl pyrrolidone and lauryl methacrylate of varying molecular weight such as of from 200,000 and 1,000,000 and described in Canadian Patent 592,974 or copolymers of vinyl pyridine and alkyl methacrylate as described in US. Patents 2,839,512, 2,889,282, 2,915,471 and 2,944,974; viscosity index improvers and pour point depressants such as the oil-soluble polymethacrylates available under the name Acryloids of the 100, 600 and 700 series and, specifically, Acryloid 150, 618, 710 and 768, described in US. Patent 2,710,842; condensation products of chlorinated paraffin wax and naphthalene; extreme pressure agents such as aliphatic amine salts of monochloromethanephosphonic acid or trichloromethanephosphonic acid, or the ester or amide of such acids; organic sulfides and mixtures thereof.

We claim as our invention:

1. A lubricating composition comprising a major amount of mineral lubricating oil and from about 0.001% to about 10% of an oil-soluble alpha-hydroxy phosphonic acid diester having the formula wherein R is an organic heterocyclic radical selected from the group consisting of and RUST-PREVENTING CHARACTERISTICS OF TURBINE BASE OILS CONTAINING AN AMOUNT OF ALPHA-IIYDROXY- METHYL PIIOSPI'IONIO ACID DIESTER OF THE FORMULA:

I /O R: f if\ O H O 0 Rs Additive with Additive with Quantity, Rust Rust with control additive (ROM P(0.1%), Rust,

percent percent R: percent 0 0/ and Rz=Ra= and Rz=Rs= 0. 1 D. 1 H-C'AHI 100 0.1 n-C4H9 0. 1 5O 11-C5Hu 10 O. 1 Traces 40 n-OaHu 5 0. 1 Traces 40 11-0 11 0 O. 1 20 n-C zH25 0 0. 05 a -s O. 1 40 11-C14H25 0 0. 1 30 11-C10H33.... 0 0. 02 (R2=C2H 0. 1 (R3==I1-CuH 5 (R2=CzH., (R m-6 H". 0.1 Traces (R3=nC H1 0 NorE.Turbiue base oil without additive shows 70% rusting of the cylindrical steel specimens.

radicals and R and R are alkyl radicals containing from 6 to 16 carbon atoms. 7

2. A lubricating oil composition comprising a major amount of mineral lubricating oil and from about 0.01% to about 5% of 2-(2,3-dihydro-gamma-pyranyl) alpha-hydroxymethyl phosphonic acid di-n-alkyl ester, said alkyl radicals containing from 6 to 16 carbon atoms.

3. A lubricating oil composition comprising a major amount of mineral lubricating oil and from about 0.01% to about 5% of 2-fury1-alpha-hydroxymethyl phosphonic acid di-n-alkyl ester, said alkyl radicals containing from 6 to 16 carbon atoms.

4. A lubricating oil composition comprising a major amount of mineral lubricating oil and from about 0.01%

10 to about 5% of 2-(2,3-dihydro-gamma-pyranyl) alphahydroxymethyl phosphonic acid diethyl-n-hexyl ester.

References Cited by the Examiner UNITED STATES PATENTS 2,460,043 1/1949 Teeters 260461 2,579,810 12/1951 Fields 260-461 2,758,971 8/1956 Mikeska 260-461 2,844,582 7/1958 Raley 260347.8 X 3,054,821 9/1962 Rolih et a1. 25249.8 X

DANIEL E. WYMAN, Primary Examiner.

LOUIS G. XIARHOS, Assistant Examiner.

Claims

1. A LUBRICATING COMPOSITION COMPRISING A MAJOR AMOUNT OF MINERAL LUBRICATING OIL AND FROM ABOUT 0.001% TO ABOUT 10% OF AN OIL-SOLUBLE ALPHA-HYDROXY PHOSPHONIC ACID DIESTER HAVING THE FORMULA