US3634242A

US3634242A - Fluorinated organic compounds as oil and distillate fuel additives

Info

Publication number: US3634242A
Application number: US784922A
Authority: US
Inventors: David S Bosniack; Stephen J Metro
Original assignee: Exxon Research and Engineering Co
Current assignee: ExxonMobil Technology and Engineering Co
Priority date: 1968-12-18
Filing date: 1968-12-18
Publication date: 1972-01-11
Anticipated expiration: 1989-01-11
Also published as: GB1262538A; FR2026493A7

Abstract

AN OIL SOLUBLE NITROGEN-CONTAININ REACTION PRODUCT OF AN AROMATIC AMINE HAVING ABOUT 6 TO 40 CARBON ATOMS AND A FLUORINATED ORGANIC COMPOUND SELECTED FROM THE GROUP CONSISTING OF A FLURINATED MONOBASIC SATURATED CARBOXYLIC ACID HAVING 2 TO 21 CARBON ATOMS AND HAVING NO SECONDARY OR TERTIARY HYDROGENS OR A FLUORINATED MONOBASIC SATURATED CARBOXYLIC ACID CHLORIDE HAVING 2 TO 21 CARBON ATOMS AND HAVING NO SECONDARY OR TERTIARY HYDROGENS INHIBITS THE CORROSIVITY OF LUBRICATING OILS AND DISTILLATE OILS AND IN ADDITION DISPLAYS LOAD CARRING ABILITY AND CLEANLINESS CHARACTERISTICS IN SUCH OILS NOT SHOWN BY SIMILAR ADDITIVE COMPOUNDS.

Description

3,634,242 FLUORINATED ORGANIC COMPOUNDS AS OIL AND DISTILLATE FUEL ADDI'IIVES David S. Bosniack, Edison, and Stephen 3. Metro, Scotch Plains, N..I., assignors to Esso Research and Engineering Company No Drawing. Filed Dec. 18, 1968, Ser. No. 784,922 Int. Cl. Cltlm 1/30, 1/32; C101 N22 US. Cl. 25233.6 14 Claims ABSTRACT OF THE DISCLOSURE An oil soluble nitrogen-containing reaction product of an aromatic amine having about 6 to 40 carbon atoms and a fluorinated organic compound selected from the group consisting of a fluorinated monobasic saturated carboxylic acid having 2 to 21 carbon atoms and having no secondary or tertiary hydrogens or a fluorinated monobasic saturated carboxylic acid chloride having 2 to 21 carbon atoms and having no secondary or tertiary hydrogens inhibits the corrosivity of lubricating oils and distillate oils and in addition displays load carrying ability and cleanliness characteristics in such oils not shown by similar additive compounds.

BACKGROUND OF THE INVENTION Field of the invention Description of the prior art Problems associated with lubricating compositions, especially those compositions prepared for use in high performance jet aircraft such as the SST engine, include its corrosivity to metals, lack of cleanliness during engine operation, and inadequate load carrying ability. Lubricating oils under the stress of high temperatures and pressures decompose into products which may corrode vital engine parts or leave harmful deposits which interfere with efiicient engine operation. Also, in jet engines, the load the lubricant is forced to bear is high. The lubricating art is filled with myriads of corrosion inhibitors and load carrying improvers, among these being certain fluorinated compounds as found 'in US. Pat. 3,269,948, and Canadian Pat. No. 764,482. These fluorinated compounds, however, have been found to be unsatisfactory, as they produce sludge and other deposits on lubricating surfaces.

SUMMARY OF THE INVENTION A new lubricating composition has been developed which demonstrates the properties of being minimally corrosive to engine parts while also exhibiting cleanliness properties and load carrying abilities not demonstrated by similar art-known compounds. This lubricating composition comprises (a) a major amount of lubricating oil and (b) a minor amount of an oil soluble nitrogen-containing reaction product of an aromatic amine having about 6 to 40 carbon atoms and a fluorinated organic compound selected from the group consisting of a fluorinated monobasic saturated carboxylic acid having 2 to 21 carbon atoms and having no secondary or tertiary hydrogens and a fluorinated monobasic saturated carboxylic acid chloride having 2 to 21 carbon atoms and having no secondary or tertiary hydrogens.

The oil soluble nitrogen-containing reaction product will be an amide or amine salt depending on whether the 3,634,242 Patented Jan. 11, 1972 'ice acid or acid chloride of the fluorinated compound is employed as a reactant material. If the fluorinated acid is the reactant, the product will be an amine salt, whereas the acid chloride will produce an amide. The fluorinated additive of this invention is prepared in the usual manner of producing amine salts or amides. The reactants are mixed together with an inert organic solvent and refluxed for a time sufficient to produce the product. The product may then be purified by art-known filtering, washing and recrystallization procedures.

The aromatic amine reactant is generally characterized as having 6 to 40 carbon atoms, preferably 6 to 28 carbon atoms. The aromatic amine may also be characterized as being polynuclear, i.e. having two or three fused rings, but preferably is mononuclear, i.e. having no fused aromatic rings. This reactant may be a polyor mono-amine, preferably a mono-amine. The aromatic amine may be primary, secondary or tertiary, preferably primary. The aromatic ring of the amine may be substituted or unsubstituted. There may be attached to the aromatic ring functional groups other than an amino group, such as alkyl hydroxy, alkoxy, halo, or ester groups. Heterocyclic amines may also be employed as reactants. Specific examples of aromatic amines include aniline, toluidine, octylaniline, bis-(octylphenyl)-amine, a,a,oc-triflll0IO-Int0- luidine, N-ethyl bis-(octylphenyl)-amine, phenyl naphthylamine, p-amino phenol, and aminoanthraquinone. Specific examples of heterocyclic amines may include 2- amino pyridine.

The preferred aromatic amine has a general structural formula:

where R is H, C, to C normal or branched alkyl, or -COOR where R is a C to C preferably C to C normal or branched alkyl group. Specific examples of these aromatic amines include methyl anthranilate, propyl anthranilate, hexyl anthranilate, ethyl p-aminobenzoate, toluidine, octylaniline and aniline.

The fluorinated acid or acid chloride reactants will preferably have 1 to 12 carbon atoms and may have a branched or normal structure, preferably normal. It is essential that no secondary or tertiary hydrogens occupy any position in the fluorinated compound, as HF may be eliminated from the molecule under the high stress of engine operation. This elimination is not likely if the hydrogen occupies a primary position at the end of the acid or acid chloride.

The preferred fluorinated reactant has the general structural formula:

Where R is selected from the group consisting of hydrogen and fluorine, preferably fluorine, Z is selected from the group consisting of hydroxyl and chloride and n is a number which varies from 1 to 20, preferably 1 to 12. This fluorinated reactant is preferably of a normal structure.

Examples of operable acid and acid chlorides include, but are not limited to, the following: trifluoroacetic acid, heptafluorobutyric acid, pentadecafluorooctanoic acid, and their corresponding acid chlorides.

The liquid lubricating oil composition of this invention will comprise a major portion of the lubricating oil, that is greater than 50 wt. percent, and 0.01 to 5 wt. percent, usually 0.1 to 3 wt. percent, based on the total weight of the composition, of the additive compounds described above. The lubricating oil composition may also be prepared in concentrate form, in which case the nitrogencontaining reaction product additive would form 10 to 80 wt. percent of the total lubricating composition.

The liquid compositions useful in this invention are mineral lubricating oils, synthetic lubricating oils and dis tillate fuels boiling in the range from about 50 F. to 750 F. Some synthetic lubricating oils include diethylhexyl sebacate, carbonate esters, glycol esters such as C oxo acid diesters of tetraethylene glycol, other diesters, silicone polymers, complex esters as, for example, the complex ester formed by the reaction of 1 mole of sebacic acid with 2 moles of tetraethylene glycol and 2 moles of Z-ethyl hexanoic acid, etc. The fluorinated additive is preferably used in synthetic ester basestocks such as esters of trimethylolpropane and normal or branched C to C monocarboxylic acids, esters of pentaerythritol and such carboxylic acids, and esters of neopentyl glycol and such carboxylic acids. The lubricating oil will have a viscosity at 210 F. in the range of to 200 SUS, preferably to 100 SUS at 210 F. and a viscosity index in the range of O to 150.

The oil-soluble nitrogen-containing additive is incorporated into the lubricating composition by dissolving it in the desired quantity into warm lubricating oil. No special procedures are required.

In addition to reducing wear and deposits in lubricating compositions, the nitrogen-containing reaction product of the aromatic amine and fluorinated acid or acid chloride may also be employed in distillate fuels for the same purpose. The liquid fuel compositions will compose a major proportion of liquid fuel (above about wt. percent) and about 0.01 to 5 wt. percent, based on the total weight of the composition of the nitrogen-containing reaction product.

The distillate fuels which may be employed include aviation turbo-jet fuels, rocket fuel (MILK-255768), gasolines, Kerosenes, diesel fuels and heating oils. Aviation turbo-jet fuels in which the amine salts of the present invention may be used normally boil between about 50 F. and about 550 F. and are used in both military and civilian aircraft. Such fuels are more fully defined by US. Military Specifications MILF-5624F, MIL-F- 25656A, MIL-F-25554A, MIL-F-25558B, and amendments thereto, and in ASTM D165562T. Kerosenes and heating oils will normally have boiling ranges between about 300 and about 750 F. and are more fully described in ASTM Specification D39648T and supplements thereto, where they are referred to as No. 1 and No. 2 fuel oils. Diesel fuels in which the amine salts may be employed are described in detail in ASTM Specification D97535T and later versions of the same specification. Gasolines which may be benefited include both motor gasolines and aviation gasolines such as those defined by ASTM Specifications D91056 and D 439-56T.

Other additives which may be used in the liquid fuel and lubricant compositions of this invention include vis- :osity index improvers, pour point depressants, corrosion inhibitors, thickeners, sludge dispersants, rust inhibitors, anti-emulsifying agents, anti-oxidants, dyes, dye stabilizers and the like.

DESCRIPTION OF THE PREFERRED EMBODIMENT The following examples are submitted as illustrating the practice of this invention. Such examples are not to be :onsidered as limiting the scope of this invention, how- :ver.

EXAMPLE I A solution of 60.5 g. (0.4 mole) methyl anthranilate n 300 ml. of anhydrous ether was charged to a 1 liter l-neck flask fitted with an air stirrer, condenser, thermom- :ter and dropping funnel. A solution of 165.7 g. (0.4 nole) pentadecafluorooctanoic acid in 300 ml. of anhylrous ether was added dropwise with rapid stirring over 1 period of 30 minutes. The mixture was stirred at reflux 4 for about 2 hours and cooled to 0 C. The product, a white precipitate, was filtered, washed with additional cold ether and dried. The crude product was recrystallized from chloroform to yield 158 g. yield) of white needles having a melting point of 124.5l25 C. The empirical formula of the expected product was An elemental analysis of the carbon, nitrogen and fluorine content was carried with these results.

Theory (percent): C, 34.00; N, 2.48; F, 50.42. Found (percent): C, 34.66; N, 2.73; F, 51.7.

This reaction product of methyl anthranilate and pentadecafiuorooctanoic acid was thus determined to be O-carboxyrnethyl anilinium pentadecafluorooctanoate, an amine salt. To parts by weight of a synthetic ester lubricating oil having as components about 70 wt. percent of an ester formed from trimethylolpropane and a C average normal carboxylic acid and about 30 wt. percent of an ester formed from dipentaerythritol and a C average normal carboxylic acid was added 0.25 part by weight of the above reaction product. Also included in the ester oil was 5.5 parts by weight of a combination of antioxidants, corrosion inhibitors and dispersants. Such commercial additives were included to more fully approximate the properties of an actual working lubricant. This fully formulated lubricant was then tested for oxidation and corrosion stability, the results of such test incorporated into Table I below.

EXAMPLE II Methyl anthranilate and heptafiuorobutyric acid were reacted according to the procedures of Example I. The purified product was a white solid having a melting point of 122.5123.5 C. T he empirical formula of the expected product was C H -O NF An elemental analysis of the carbon and fluorine content was carried out with the following results.

Theory (percent): C, 39.46; F, 36.42. Found (per cent): C, 39.46; F, 36.9.

The reaction product was thus determined to be O-carboxymethyl anilinium heptafluorobutyrate, an amine salt.

The reaction product of this example was added to the lubricant of Example I and the lubricant tested for oxidation and corrosion stability. The results of this test are recorded in Table I.

TABLE I Oxid.-c0rr. stability test 425 F./72 hrs.

Ihe base oil is the oil of Example I taken without the amine salt additive.

The 425 F Oxidation-Corrosion-Stability Test was carried out by blowing air at the ratio of 5 liters per hour through 100 grams of the lubricating composition maintained at a temperature of 425 F. for 72 hours. At the end of the test, the percentage increase in viscosity and change in total acid number (T.A.N.) were determined. The corrosive characteristics of the lubricant were determined by immersing various weighed metal coupons in the oil and measuring weight change at the end of the test. The change in weight signifies either corrosion due to dissolving of the metal or weight gain due to deposits. The test is used to determine if lubricants offer suificient protection for critical metal components of engines and accessories when operated at high temperatures.

From the data in Table I it an be readily seen that the additive reaction products of Examples I and II dramatically reduce magnesium corrosion.

EXAMPLE III To a liter 4-neck flask fitted with a stirrer, condenser, thermometer and funnel was charged 432.6 g. (1.0 mole) pentadecafluorooctanoyl chloride, 1600 ml. of dry toluene and 158 g. pyridine. This mixture was heated to 90 C. and a hot (about 80 C.) solution of 165.2 g. (1.0 mole) ethyl p-aminobenzoate dissolved in 1400 ml. toluene added over a 30-minute period. This mixture was then refluxed for four hours and filtered hot through a steam-jacketed Buchner funnel. The filtrate was then cooled to 20 C., which resulted in the crystallization from solution of a pink solid. The crude product was filtered from solution and recrystallized from 2 liters of toluene to yield 440 g. (78.5% yield) of white needles having a melting point of 127.5-129" C.

As some pyridine hydrochloride was still present in this product, further purification was necessary. Two hundred fifty grams of the product was dissolved in acetone and filtered. The filtrate was added dropwise with stirring to 450 ml. of distilled water to precipitate the product. A solution of 75 parts acetone and 45 parts water was added to facilitate the stirring, which was continued for one hour. The resulting white solid was filtered, washed with an acetone-water solution and dried to constant weight. A white solid weighing 230 grams was obtained.

The empirical formula of the expected product was C1qH11O3NF15. An elemental analysis of the carbon fluorine and chloride was carried out with the following results:

Theory (percent): C, 36.38; F, 50.78; Cl, nil. Found (two trials), percent: C, 36.65, 36.90; F, 52.1, 49.5; Cl, 0.01, 0.03.

The reaction product was then determined to be ethyl (p-pentadecafiuorooctanamido) benzoate, an amide.

To determine the cleanliness of lubricating compositions containing the aromatic reaction product of the invention, such compositions were subjected to the Type II Bearing Rig Test. For purposes of comparison, lubrication compositions containing the aliphatic amine salt of US. 3,269,948 were also tested. The results of these tests are listed in Table II.

TABLE II Type II Bearing Big Test Demerit Avis. @100 Lubricant composition rating F., percent AT.A.N.

Oil A l 82. 5 266 6. 34 Oil A (100 parts by Wt.) plus 2 parts by wt. auxiliary additive 86. 2 212 4. 49 011 B 4 (100 parts by Wt.) plus 1 part by wt. auxiliary additive 2 plus 0.5 parts by Wt. PFAS-820 106. 9 191 4. 74 Oil B (100 parts by wt.) plus 0.25

part by Wt. PFAS-SAN 5 S2. 9 230 6. 26 011 B (100 parts by wt.) plus 0.25

part by wt. FAB B 78. 4 220 5. 86

1 Oil A is a conventional lubricant composition having a synthetic ester base plus various conventional antioxidants, dispersants, and corrosion inhibitors.

2 Auxiliary additive, a dimer acid derivative.

3 PEAS-820 is the amine, a reaction product ofpentadecafluorooctanoic acid and Primene .IM-T, the aliphatic amine RNH2 where R is a mixture of isomers having 18-22 carbon atoms with a tert-alkyl structure.

4 011 B is a conventional lubricant composition having a synthetic ester base plus various conventional antioxidants, dispersants and corrosion inhibitors.

5 PEAS-SAN is the amine salt of Example I.

FAB is the amide of Example III.

In a Type II Bearing Rig Test a 100 mm. diameter aircraft type steel roller bearing rotation at 10,000 r.p.m. is maintained at a temperature of 500 F. while being sprayed with a jet of the oil composition heated to a temperature of about 440 F. in a sump so as to have a jet temperature of 400 F. The oil falls oil the bearing into a reservoir or sump where it is picked up by a pump and recirculated. The total amount of oil in the circulating system is about 2 gallons. The viscosity of the oil is checked at 10 hour periods until a period of 100 hours has passed. Oils showing good oxidation stability will show very little change in viscosity and total acid number during the hearing test, while oils poor in oxidation stability will tend to break down and rapidly increase in viscosity and total acid number. Also at the end of the hour test, the bearing is examined for cleanliness.

Cleanliness is determined by the amount of deposits on bearing parts. The parts are visually inspected and each part given a rating from 0 to 20, with 0 being clean. Each bearing part is weighted in importance and a total rating called a demerit rating compiled for the entire bearing assembly. The lower the demerit rating, the cleaner the bearing assembly. This procedure can be found in Method No. 3410 of Federal Test Method Standard Number 791. The oil temperature in a Type II test is 440:5 F.

No substantial difference in change in viscosity or total acid number is observed between the aliphatic and aromatic additives. The advantage of the aromatic reaction product over the aliphatic reaction product can be seen by comparing the demerit rating results obtained. The demerit rating for oils containing the additive of Example I and Example III was 82.9 and 78.4 respectively, while the demerit rating for the oil containing the aliphatic salt was 106.9. This represents about a 15% improvement over oils containing aliphatic salts, which is a significant improvement. The effect of the auxiliary additive on demerit rating is essentially negligible, as can be seen from comparing its elfect in Oil A in Table II.

EXAMPLE IV According to the procedure of Example I, an amine salt of morpholine and pentadecafluorooctanoic acid was prepared. The salt had a melting point of 110.5111.5 C.

According to the procedures of Example I an amine salt of 2-amino pyridine and pentadecafluorooctanoic acid was prepared. The salt had a melting point of l35137 C.

According to the procedures of Example I an amine salt of p-amino phenol and pentadecafiuorooctanoic acid was prepared having a melting point of 201-205" C.

According to the procedures of Example I an amine salt of l-aminoanthraquinone and heptafluorobutyric acid was prepared having a melting point of 142145 C.

According to the procedures of Example I, an amine salt of benzotriazole and pentadecafluoroctanoic acid was prepared having a melting point of 6870 C.

According to the procedures of Example III, an amide was prepared from butyl p-amino benzoate and pentadecafluorooctanoic acid having a melting point of 113.5- 115.5 C.

The amine salt and amide products described in this example are thus added to mineral or synthetic base lubricating oils in amounts ranging from 0.01 to 5 wt. percent, based on the total lubricating composition, to form lubricants having improved corrosivity and cleanliness properties.

The eifect of the fluorinated organic compound described herein on the load carrying ability of the lubricating compositions of this invention was determined through Ryder Gear Load Tests. The results of these tests are recorded in Table III below:

1 The base oil is Oil A of Table II.

The Ryder Gear Loads test number is Federal Test Method Standard No. 791, Test No. 6508. From the data of Table III it can be seen that the fluorinated material I I I I I of the lubricating composition of this invention imparts I I I I I I I 5. A lubricating oil composition as claim 4 wherein I iI :I I i I: I I I excel'lentload carryingabilityto that composition. I 1 I R is afluorine atom. I I I I I I I I I I I I I I I I What is claimedis: I I II I I i '6.:A 1uhricating' oil :cornposition as inelaim. 5 wherein I I I 1,A iiquidoompositioncomprising:' RoftheIaromatinamine--COOR i (a) aimajor amount-of a liquid seIlectedlfrIor-n the group 5 A lubricating oil composition as inclai-m- 6 wherein z s I I I I :I I I I I I I I I consisting of lubricatingoils and distillate fuels boil i l f 3 th'el ubricatingoil is a -sy ntheticIoil-.. I I I I I I I I I I I I I I I-.-.'. inginthe range-of SO IFJtO' :750'F.; and- I i I 3 I I I I I I I I 8:. A lubricating Oil domposition as inclaim 7 wherein I I ?I II I I I I i I i I (b )-abiout IO1:to Iwt .ipercent, based on-the total weight the-fluorinated organic compoundreactant has a n'ormal 1 f I I of theIcomposition,ofI(1)anamide'ofafluorinated- -structure. t I I I II I I I I I I I I I monobasic saturated carboxylic' acid chloride having I I I I A lubricating oil composition as? in-claim- 8 wherein: I I I I I I I t' '2; toi2l carbon-atoms;andihaving;nosecondaryori 'nvariestfromltolii I I I I I I I I tertiary. hydrogen atoms and an aromatic amine haw I I I I I I I 10; A Ilubrisatingoil composition as in claim 9 wherein I I I I .in'g6 to 40carbonatoms'or(zyanaminesaltofia R isaC toC normala1ky1group; I I i I f I i lluminated monobasieisaturated carboxylic acid hav-: I I I I ILA lubricating oilcornposition as in claim 10 wherein I II 1 I ing Z to. 21 carbon atoms and having Ito-secondary R 'is Ie thyL I III I I I I I I I I I I I or tertiary hydrogen atoms and anaromatic amine I I I I I 1 1 A lubricating oil composition asrin claim 1:1 wherein: I r I 2 I 2 I I I I I I I I having 6 10.140 carbon atoms-III I I I I I I I I I I I I :the fiuorinated organic reactant is pentaclecafiuorooctanoicI I I ..2.-A-iiquidlcompositionasIinclaimlwhereintheiaroen I acidI I I- I I II II I matic amine has the general structural formular I I I I I I I I i I I I I I 13. A lubricating oil composition as in claim 12 wherer I I I I I I I II I I I I '20illZiSCh1QFid6."' I

I I I I I I I I I i i I I -@111}; Arr additive Iconcentrate comprisinga lubricating; I I: I I I I I I I I I I I I I I I I I I I I I I I I oiIand f1-om 1(1toBOwtupercentofthenitrogen-con tain-= i I I I I I 1 l 1 NH2 I I 1 1 I I ing reaction product of claim 13. I

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