US3759829A

US3759829A - Functional fluid compositions

Info

Publication number: US3759829A
Application number: US00156133A
Authority: US
Inventors: J Sullivan
Original assignee: Monsanto Co
Current assignee: Monsanto Co
Priority date: 1966-04-06
Filing date: 1971-06-23
Publication date: 1973-09-18
Anticipated expiration: 1990-09-18
Also published as: FR1517601A; US3752764A; BE696664A; ES338687A1; GB1192910A; GB1188813A; IL27743A; DE1644909A1; NL6704601A; US3788992A; US3591500A; US3939084A; BR6788302D0

Abstract

FUNCTIONAL FLUID COMPOSITIONS COMPRISING POLYPHENYL THIOETHERS, MIXED POLYPHENYL OXY-THIOETHERS AND MIXTURES THEREOF CONTAINING CERTAIN PYRIMIDINES AS ANTI-CORROSIVE AGENTS HAVE IMPROVED METAL COMPATIBILITY AND ARE PARTICULARLY USEFUL AS AIRCRAFT ENGINE LUBRICANTS AND HYDRAULIC FLUIDS.

Description

United States Patent US. Cl. 252-475 10 Claims ABSTRACT OF THE DISCLOSURE Functional fluid compositions comprising polyphenyl thioethers, mixed polyphenyl oxy-thioethers and mixtures thereof containing certain pyrimidines as anti-corrosive agents have improved metal compatibility and are par ticularly useful as aircraft engine lubricants and hydraulic fluids.

This application is a continuation-in-part of application Ser. No. 796,885, filed Feb. 5, 1969, now US. Pat. No. 3,591,500 dated July 6, 1971, which in turn is a continuation-in-part of application Ser. No. 540,488, filed Apr. 6, 1966, now abandoned.

This invention relates to functional fluid compositions having improved metal compatibility and more particularly to functional fluids containing certain organic nitrogen compounds.

Many different types of materials are utilized as functional fluids and functional fluids are used in many different types of applications. Such fluids have been used as electronic coolants, atomic reactor coolants, diffusion pump fluids, synthetic lubricants, damping fluids, bases for greases, force transmission fluids (hydraulic fluids) and as filter mediums for air-conditioning systems. Because of the wide variety of applications and the varied conditions under which functional fluids are utilized, the properties desired in a good functional fluid necessarily vary with the particular application in which it is to be utilized with each individual application requiring a functional fluid having a specific class of properties.

Of the foregoing, the use of functional fluids as lubricants, particularly aircraft engine lubricants, has posed a difficult area of application. Present design trends in aircraft engines are to the pure jet type or turbofan and away from the turboprop engine. Aside from the mechanical differences in design between the turbofan and turboprop engines, there is a significant difference in the properties of the lubricants required for these engines, primarily because of increased operating temperatures. Furthermore, even within the area of turbofan engine design alone, there is a trend to increase the temperatures at which a lubricant must operate. Present temperature levels for turbofan lubricants are of the order of 400-450 F. (bulk oil temperature). However, it is evident that within the near future, temperatures of the order of 5 00 F. or higher will be commonplace.

As the operating temperatures for lubricants have increased, it has become exceedingly difficult to find lubricants which properly function at these higher temperatures for any satisfactory length of time. Furthermore, it should always be realized that while the operating temperatures generally referred to are bulk oil temperatures, the actual temperatures at the points requiring lubrication exceed the bulk oil temperature and oftentimes are one hundred to several hundred degrees higher.

In addition to the high temperature stability or durability problem, that is, the problem of finding a lubricant which will be thermally and oxidatively stable at temperatures as high as 500 F., the solution of this problem is further complicated by the fact that in order for a lubricant to be satisfactory for use in many aircraft engines, it must also be usable at temperatures as low as -20 F. to 0 F. It is, therefore, evident that present trends require lubricants having not only an exceedingly wide liquid range but lubricants which are also thermally and oxidatively stable at high temperatures. Furthermore, present and future lubricants must, of course, possess at least adequate temperature-viscosity properties and satisfactory lubricity, that is, the lubricants must not become too thin at the very high temperatures to which they are subjected nor must they become too thick at the lower temperatures and must at the same time be able to provide at least minimum lubricity over such range of temperatures. In general, such lubricants must also not be too volatile and even if somewhat volatile must not, upon evaporation, leave any significant deposits to interfere with the proper operation of engine bearings.

Other properties which must be possessed by satisfactory jet engine lubricants are low pour point and relatively high flash point and autogenous ignition temperatures.

Another lubricating problem associated with presentday design and design trends in jet engines is that the increased thrust needed to obtain high speeds and altitudes results in further increases in not only operating temperatures but also higher bearing pressures.

A further problem in obtaining a lubricant which has good combination of properties at various temperatures is that those materials having a low pour point also have a high evaporation rate at the temperatures of the order of 400 F. 500 F.

In summary, as discussed above, a satisfactory jet engine lubricant must possess a wide variety of properties. Furthermore, all of these properties are not only difficult to obtain in the same fluid but some of them tend to be mutually exclusive.

The most important properties for jet engine lubricants mentioned above are high temperature stability (thermal stability), high temperature oxidative stability and little or no corrosion toward metals. While fluids are known which possess adequate thermal and oxidative stability either inherently or can be provided by incorporating additives, many such functional fluids are corrosive to metals at high temperatures in the order of 500 F. and in particular to copper and ;ilver. Although many additives, including organic nitrogan compounds, have been used in the past to reduce or eliminate the tendency of lubricants to corrode metals at lower temperatures, i.e., to 350 F, at the higher temperatures referred to above the properties of additives become unpredictable. Many previously known metal corrosion inhibitors are not active at elevated temperatures and in many instances where they retain their corrosion inhibiting properties, they cause other problems such as descreased thermal and oxidative stability.

Additives useful in many different chemical types of functional fluids have now been discovered which reduce or eliminate the corrosiveness of the fluids toward metals at high temperatures.

It is, therefore, an object of this invention to provide functional fluid compositions which are substantially noncorrosive to metals. Another object of this invention is to provide functional fluid compositions which are substantially non-corrosive to metals at high temperatures. Another object of this invention is to provide additives for functional fluids which when added in a small amount to a base stock will reduce or eliminate the copper corrosivity of the fluid.

The objects mentioned above and others, which will hereinafter be apparent, are accomplished by adding to functional fluids, hereinafter described, corrosion reducing amounts of an organic nitrogen compound selected from the group consisting of (A) A compound represented by the formula wherein X is selected from the group consisting of hydrogen, NH and -OH, Y is selected from the group consisting of hydrogen, NH OH and NHCEN and G, G and G are each selected from the group consisting of carbon and nitrogen provided that at least 1 of G and G" is carbon and at least 2 of G are carbon, Z is selected from the group consisting of hydrogen and a hydrocarbon group, n is an integer from 1 to 2, m is an integer from 1 to 2 and the sum of m-l-n is equal to the number of G groups that are carbon.

(B) A compound represented by the formula where G is selected from the group consisting of carbon and nitrogen provided that from 2 to 4 of G is nitrogen, X is selected from the group consisting of hydrogen, NH and OH, and p is an integer from to 2 and is no greater than the number of carbon atoms in the ring represented by G.

(C) A compound represented by the formula 0 R1 N% NCR where each R, R and R are selected from the group consisting of hydrogen and NH and (D) A compound selected from the group consisting of cyanoamino hydroxy pyrimidines, anilinopropionitriles, aninocarbazols, aminopyridines, aminonicotinic acids, cyanoglutaramides, aminonaphthylimides and alkyldiimidazolines.

The hydrocarbon group, Z above, can be an aliphatic or aromatic hydrocarbon.

Preferred additives of this invention are compounds of A above represented by the formula z Tit where X, Z, n and m have the same meaning as in A above.

Examples of compounds of Formula I above are 4- aminoindazole, 5 aminoindazole, 6-aminoindazole, 7- aminoindazole, 4 hydroxyindazole, 5 hydroxyindazole, 6 hydroxyindazole and 7 hydroxyindazole. Such compounds are preferred additives of this invention because they are more soluble in the base stocks disclosed herein, particularly polyphenyl thioethers, and can be employed in small amounts to prevent or reduce metal corrosion. Particular compounds of A to D are presented in Table I hereinafter set forth.

The amount of the additives of this invention which are used in functional fluids vary according to the nature of the particular fluid to which they are added, i.e., the amount is proportional to the corrosivity of the fluid. Thus, the corrosivity of some fluids can be significantly reduced or eliminated by the addition of as little as about 0.025% by weight of the base stock of an additive of this invention. In general, an amount of up to about 5% by Weight is adequate to achieve a substantially noncorrosive fluid. It is preferred to use from about 0.05% to about 0.5% by weight of an additive of this invention since within that range of concentrations the amount of additive used is low enough so that solubility considerations are not limiting yet adequate corrosion inhibition is obtained.

Because of the various considerations which go into the choice of the amount of additive use and also because of the differences existing between the many fluids in which the additives of this invention are active, the amount of additive to be used can be expressed as a corrosion reducing amount, i.e., an amount which is effective to provide decreased corrosivity of the fluids contemplated.

Since many of the additives of this invention have limited solubility in some of the fluids hereinafter described, the improved compositions of this invention can be prepared by dissolving the additive in a small portion of the fluid at elevated temperatures in the range of from about F. to about 200 F., then mixing the heated composition with the main portion of the fluid to form a composition of this invention.

The additives of this invention are particularly useful in polyphenyl thioethers, which as used herein, means a compound or physical mixture of compounds represented by the structures where m is a whole number from 0 to 6,

(III) I E-S E flnaFE I where A and A are each selected from oxygen and sulfur,

where x and y are whole numbers from 0 to 3 and the sum of x-i-y is from 1 to 6 and A and A are each selected from oxygen and sulfur but at least one of A and A is sulfur, and

where R is selected from the group consisting of alkyl and alkoxy groups having from 1 to 4 carbon atoms, hydroxyl and hydrogen, T is selected from the group consisting of alkyl, haloalkyl and alkoxyl groups having from 1 to 4 carbon atoms, and hydroxyl, A is selected from the group consisting of oxygen and sulfur provided at least one A is sulfur, y, m and n are integers from 1 to 3 and K is an integer from 0 to 1 providing at least one K is 1.

Examples of such polyphenyl thioethers are:

(XIII) Preferred compositions of this invention in which additives of this invention are advantageous are mixtures of m-bis(phenylmercapto)benzene and certain other materials which have properties that make them well suited [for the uses disclosed above and particularly those applications, such as jet engine lubricants, requirin high temperatures, thermal and oxidative stability and Wide liquid range. The other materials contemplated to be used with m-bis(phenylmercapto)benzene to provide such mixtures are as follows:

(a) The three-, four-, five-, and six-ring polyphenyl thioethers, for example O-bis (phenylmercapto) benzene bis-(-m-phenylmercaptophenyl) sulfide @UU O 6 m phenylmercaptophenyl p phenylmercaptophenyl sulfide,

VIII O-st j-st l st J the trisphenylmercaptobenzenes,

Q- Q Q such as 1,2,4-trisphenylmercaptobenzene,

3,3 -bis(phenylmercapto)biphenyl m-bis(p-phenylmercaptophenylmercapto)benzene,

m-bis (m-phenylmerc aptophenylmercapto benzene Q U U U O and bis[m-(m phenylmercaptophenylmercapto)phenyl] sulfide E TSAE TSI ]SI ]SI TS/E (b) The mixed polyphenyl oxy-thioethers having the formula wherein R is a phenyl group, R is a phenylene group and Y and Y are each selected from the group consisting of oxygen and sulfur, providing at least one of Y and Y is sulfur and m is a whole number from 1 to 4. Examples of such mixed polyphenyl oxythioethers are m-phenylmercaptodiphenyl ether (Tim 3,3'-bis(phenylmercapto)diphenyl ether,

uuuu

3,3'-bis (phenoxy)diphenyl sulfide,

3-phenoxy-3'-phenylmercaptodiphenyl sulfide,

un on 3-phenylmercapto-3'-phenoxydiphenyl ether,

(WWW

3,4'-bis(phenylmercapto) diphenyl ether,

new

m-bis(m-phenylmercaptophenoxy)benzene,

(XX) O-sf J-of ]s( ]s and 3-phenylmercapto 3 (m phenylmercaptophenylmercapto) diphenyl ether,

Q- Q- Q QQ (c) The four-, fiveand six-ring polyphenyl ethers which can be represented by the structure lulu (XXIII) such as 3,3'-bisphenoxy biphenyl and by the structure such as 1,3,4-triphenoxybenzene and mixtures and combinations of (a) through (c).

The Compounds (a) through (c) can be used alone or in combination to form compositions of this invention.

A typical mixture of polyphenyl thioethers is one which contains by weight from about 45% to about 55% mphenoxyphenyl m-phenylmercaptophenyl sulfide, from about 25% to about 35% bis(m-phenylmercaptophenyl) sulfide and from about 18% to about 25% bis(m-phenoxyphenyl)sulfide. Particularly useful mixtures of polyphenyl thioethers are those containing the above mixtures and mbis(phenylmercapto)benzene in about equal proportions. More particularly, examples of mixtures containing polyphenyl thioethers, mixed polyphenyl ethers, thioethers and halogenated polyphenyl ethers which are suitable as lubricants under high temperature conditions are as follows in weight percent:

Percent m-Bis(phenylmercapto)benzene 50 m-Phenoxyphenyl-m-phenylmercaptophenyl sulfide 25 Bis(m-phenoxyphenyl)sulfide l1 Bis(m-phenylmercaptophenyl)sulfide 14 Percent m-Bis(phenylmercapto)benzene 50 m-Phenoxy-m-phenylmercapto benzene 25 o-Bis(phenylmercapto)benzene 25 Percent m-(m-Chlorophenylmercapto) m phenylmercapto benzene 46 m-Bis(pheny1mercapto)benzene 31 m-Phenoxy-m-phenylmercapto benzene 15 m-Chlorodiphenyl sulfide 8 It is also contemplated that any of the individual polyphenyl ethers described above or mixtures thereof in admixture with additives of this invention can also be utilized to provide compositions of this invention. For example, mixtures of polyphenyl ethers in which the non-terminal phenylene rings are linked through oxygen atoms in the meta and/ or para positions, have been found to be particularly suitable. An example of such polyphenyl ether compositions are those containing, in percent by weight, from about 0 to 6% of o-bis(m-phenoxyphenoxy)benzene (1), about 40 to 85% of m-bis(m-phenoxyphenoxy)benzene (2), about 0 to 40% of m-[(m-phenoxyphenoxy) (pphenoxyphenoxy)] benzene (3), about 0 to 12% of p-bis (m-phenoxyphenoxy)benzene (4), about 0 to 10% of p- [(p phenoxyphenoxy) (m phenoxyphenoxy)]benzene (5), and about 0 to 6% of m-bis(p-phenoxyphenoxy)benzene (6). Typical compositions of such mixtures are listed below. The number of parentheses refers to the compound mentioned above having the same number thereafter.

TYPICAL COMPOSITIONS Mixtures percent by weight of components A B C D Component:

Ester fluids with particularly advantageously low temperature viscosity properties, which flow readily at temperatures as low as 30 F., are provided by the diesters of dibasic acids. Ester lubricants of the dibasic acid ester type are illustrated by diesters of long-chain dicarboxylic acids like azelaic acid with long-chain branched primary alcohols of the C to C range. The synthetic ester lubricants also include the esters of long-chain monobasic acids such as pelargonic acid with glycols such as polyethylene glycols. Complex esters are also formed by linking dibasic acid half esters through a glycol such as dipropylene glycol, a polyethylene glycol of 200 molecular weight, and so forth. Permutation and combination of these methods of forming polyester type lubricant fluids are valuable as well and also it is common practice to achieve desired properties in the ultimate base fluid by blending ditferent polyester products. Simple esters providing suitable fluids can be exemplified, for example, by bis (Z-methylbutyl sebacate, bis l-methylcyclohexylmethyl)sebacate, bis(2,2,4-trimethylpentyl)sebacate, dipropylene glycol dipelargonate, the diesters of acids such as sebacic, azelaic and adipic acid with complex C -C primary branched chain alcohols such as those produced by the x0 process, polyethylene glycol 200 bis(Z-ethylhexyl) sebacate, diisoamyl adipate, 1,6-hexamethylene glycol di- (Z-ethylhexanoate, bis(dimethylamyl)azelate and so forth.

Ester fluids with particularly good high temperature oxidation resistance are provided by neopentyl polyol esters. The alcohols from which these esters are derived have the carbon structure of neopentane, with a central carbon atom surrounded by 4 substituent carbon atoms. Included in the neopentyl polyols are neopentyl glycol, trimethylolethane, trimethylolpropane, pentaerythritol and dipentaerythritol. Generally, the base fluids comprising neopentyl polyol esters are the esters With monocarboxylic acids. Such esters are generally more oxidatively and thermally stable than the dibasic acid esters. The useful esters of the neopentyl polyols include, for example, the esters of trimethylol propane, neopentyl glycol, pentaerythritol and dipentaerythritol with normal, branched chain and mixed acids having the chain lengths varying from C to C Thus, an illustrative series of esters are trimethylolpropane tri-n-pelargonate, trimethylolpropane, tricaprate, trimethylolpropane tricaprylate, the trimethylolpropane triester of mixed octanoates, pentaerythrityl tetra butyrate, pentaerythrityl tetravalerate, pentaerythrityl tetracaproate, pentaerythrityl dibutyrate dicaproate, pentaerythrityl butyrate caproate divalerate, pentaerythrityl butyrate trivalerate, pentaerythrityl butyrate tricaproate, pentaerythrityl tributyrate caproate and mixed tetraesters of C fatty acids. Suitable dipentaerythrityl esters include dipentaerythrityl hexabutyrate, dipentaerythrityl hexapropionate, dipentaerythrityl hexavalerate, dipentaerythrityl hexacaproate, dipentaerythrityl hexaheptoate, dipentaerythrityl hexacaprylate, dipentaerythrityl tributyrate triacaproate, dipentaerythrityl trivalerate trinonylate and other dipentaerythrityl mixed hexaesters of C fatty acids. Also, additives of this invention are useful in mixtures of monoand dipentaerythritol esters of C fatty acids and mixtures of C fatty acids.

For further description of still other ester fluids adapted for use as lubricant base stocks and useful in the provision of the compositions of this invention, reference may be made, for example, to the discussion in Gunderson et al., Synthetic Lubricants (Reinhold, 1962).

Other compositions of this invention useful as functional fluids can be prepared by combining additives of this invention described above with monoand dialkylthiophenes represented by the structural formula 10 wherein A, B and D are each alkyl C radicals and any two of A, B and D radicals together with the carbon atom to which they are attached can form an alicyclic ring and m and n are integers from 0 to 1, providing the sum of "17+?! is at least one.

Typical thiophenes of structure XXVII are as follows:

Other functional fluids in which the additives of this invention can be used are blended synthetic fluids comprising a major proportion of dihalogenated diphenyl ethers or sulfides and a minor amount of blending agents selected from halogenated lower alkyl benzenes, halogenated benzene, monohalogenated diphenyl ethers and chlorinated biphenyl or combinations thereof. The dihalogenated diphenyl ethers suitable for use as base stocks in the fluid compositions of this invention are those represented by the structure (X XV III) F where A is a chalkogen having an atomic number of 8 to 16, E and F are bromine, chlorine and fluorine.

Typical examples of such ethers and sulfides are:

(1) Different halogen on each ring 2-bromo-2-chlorodiphenyl ether, 2-bromo-2-chlorodiphenyl sulfide, 2-bromo-3'-chlorodiphenyl ether, 2-bromo-3'-chlorodiphenyl sulfide, 2-bromo-4-chlorodiphenyl ether, 2-bromo-4-chlorodiphenyl sulfide, 3-bromo-2'-chlorodiphenyl ether, 3-bromo-2'-chlorodiphenyl sulfide, 3-brom0-3'-chlorodiphenyl ether, 3-fluoro-3'-fluorodiphenyl sulfide, 3-fluoro-4-chlorodiphenyl ether, 3-bromo-4-fluorodiphenyl sulfide, 4-fluoro-3-fluorodiphenyl ether, 4-brorno-3'-chlorodiphenyl sulfide, 4-bromo-4'-chlorodiphenyl ether, 4-bromo-4'-chlorodiphenyl sulfide, 4-bromo-2'-chlorodiphenyl ether, and 4-br0m0-2'-chlor0diphenyl sulfide.

(2) Same halogen on each ring 2,2'-dibromodiphenyl ether, 2,2'-dibromodiphenyl sulfide, 2,3'-dibromophenyl ether, 2,3-dibromodiphenyl sulfide, 2,4-difiuorodiphenyl ether, 2,4-difluorodiphenyl sulfide, 3,3'-dibromodiphenyl ether, 3,3-dibromodiphenyl sulfide, 3,4-dibromodiphenyl ether, 3,4'-dibromodiphenyl sulfide, 4,4-dibromodiphenyl ether, 4,4'-dibromodiphenyl sulfide, 2,2-dichlorodiphenyl ether,

11 2,2'-dichlorodiphenyl sulfide, 2,3'-dichlorodiphenyl ether, 2,3'-dichlorodiphenyl sulfide, 2,4'-dichlorodiphenyl ether, 2,4'-dichlorophenyl sulfide, 3,3'-dichlorodiphenyl ether, 3,3'-dichlorodiphenyl sulfide, 3,4'-dichlorodiphenyl ether, 3,4-dichlorodiphenyl sulfide, 4,4'-dichlorodiphenyl ether, 4,4'-dichlorodiphenyl sulfide.

As used herein the term major amount of a fluid means that the amount of a particular fluid in a specific formulation is at least equal to the amount of any particular blending agent in said formulation. On the other hand the term minor amount of a blending agent means that the amount of a particular blending agent in a specific formulation is no more than the amount of any specific fluid in said formulation.

The ethers are generally preferred over the sulfides because their lower melting points make them usable in a wider number of applications and of the ethers, those in which the halogen substituents are in the 3,4-relationship are preferred for use in the compositions of this invention, because their low melting points are the lowest of all the fluids of this invention.

The blending agents which can be used include the halogenated lower alkyl (C benzenes containing 1 to halogens, such as 4-bromomethylbenzene, 2-bromoethylbenzene, 4-bromopropylbenzene, 4-chlorobutylbenzene, 2,4-dichloromethylbenzene, 2,3-dibromoethylbenzene, 2,4-dibromoethylbenzene, 2,4-dichloroethylbenzene, 2-fluoro-4-chloroethylbenzene, 2,5-dibromoethylbenzene, 3,4-dibromoethylbenzene, 3,S-dibromopropylbenzene,

2,4'-fluorobutylbenzene and the like. It is preferred to use the bromine-containing compounds because of the increased fire-resistance obtained thereby. Further examples of halogenated alkyl benzenes are triand tetrachlorethylbenzene, triand tetrabromoethylbenzene, pentachloromethylbenzene, pentachloroethylbenzene, pentabromoethylbenzene, pentabromopropylbenzene, pentachlorobutylbenzene and the like.

In addition to the use of specific compounds, there can be used a mixture of halogenated alkyl benzenes such as the mixture of brominated ethyl benzenes disclosed in US. Pat. No. 2,257,903, which contain an average of two atoms of bromine per mol of ethyl benzene.

Other blending agents include the monohalogenated diphenyl ethers such as 2-chlorodiphenyl ether, 3-chlorodiphenyl ether, 4-chlorodiphenyl ether, 3-bromodiphenyl ether and the like and chlorinated biphenyl which is i1- lustrated by the chlorinated biphenyl commercially available as products containing about 21%, 32%, 42%, 48%, 54% and 60% of combined chlorine corresponding approximately to mono-, di-, tri-, tetra-, pentaand hexachlorobiphenyl, respectively. The expression chlorinated biphenyl containing a stated percentage of combined chlorine is used herein as not only including these directly chlorinated products, but also as blends of one or more chlorinated biphenyl whereby the total chlorine content is broadly within the range of to 60% preferably with the range of 20% to 42% by weight. It is also preferred, in order to obtain fluids having low crystallizing points, to use chlorinated biphenyl which has been isomerized, and preferably distilled thereafter according to the teachings of US. Pat. No. 3,068,297.

The halogenated benzenes which can be used as blending agents include chloro and bromobenzenes. The preferred chlorobenzenes are di-, triand tetrachlorobenzene and mixtures thereof. The preferred bromobenzenes are mono-, diand tribromobenzene and more particularly m-dibromobenzene. Typical examples of halogenated benzenes useful as blending agents are o-dichlorobenzene, m-dichlorobenzene, 1,2,3 trichlorobenzene, 1,2,4 trichlorobenzene, 1,3,5-trichlorobenzene, 1,2,3,4-tetrachlorobenzene, 1,2,3,S-tetrachlorobenzene, o-dibromobenzene and 1,2,4-tribromobenzene.

Other blending agents which can be used are perhalogenated alkyl compounds such as hexachlorobutadiene.

Another class of functional fluids employed in preparing compositions of this invention are aliphatic hydrocarbon oils. Such oils are those obtained by super refining petroleum thereby producing a mixture of saturated aliphatic hydrocarbons or they can be produced synthetically. Preferred hydrocarbon oils useful in preparing compositions of this invention are those represented by the formula wherein R R R and R are saturated hydrocarbon radicals having a combined total of from 4 to carbon atoms. The number of variations of the R groups in Formula XXIX is very large, and dependent thereupon is the viscosity range of any particular fluid. To list by name the many compounds contemplated by the above structure would unduly lengthen the present disclosure so therefore the following named compounds conforming to Formula XXIX are included herein only to point out the more commonly available and more desirable members of the class of compounds and in no way is such listing intended to exclude other compounds conforming to said formula. Such exemplary compounds are:

2, 2,4-trirnethylpentane, 4,4,6-trimethylnonane, 7,9-dibutyl-7-methylpentadecane, 9,11-dihexyl-9-methylnonadecane,

1 1,13 -dioctyl-1l-methyltricosane,

13 .15-didecyl-13-methylheptacosane,

15 1 7-didodecyl-1S-methyldotriacontane, 4-ethyl-2,4-dimethylp entane, 4-butyl-4,6-dimethylnonane, 7-methyl-7-butyl-9-ethylpentadecane, 9-rnethyl-9-pentyl-1l-propylnonadecane,

1 l-methyl-l l-hexyl-13-tridecyltricosane, 13-methyl-13-heptadecyl-15-nonylheptacosane, IS-methyl-15-buty1-17-hexyldotriacontane.

One of the major bench scale methods usedf or evaluating the corrosivity of a lubricant or hydraulic fluid is the procedure given in MIL-L-923 6A according to which the lubricant to be treated is heated at a specified temperature in the presence of certain metals and air and the corrosivity determined by measuring the change in weight of the metals.

Various compositions of this invention were tested according to the procedure of MILL-9236A except that the temperature was held at 500 F. instead of 600 F. The metal specimens used were, as specified in said procedure, steel, copper, silver, titanium, magnesium alloy and aluminum alloy. However, only the results upon copper and silver are reported since the compositions tested had essentially no effect on steel, titanium, magnesium alloy and aluminum alloy. The results observed using the above-described procedure are recorded in the tables below. The corrosivity to metals was determined by weighing the metal specimens before and after the test. The weight difference in milligrams per square centimeter of metal surface exposed to the fluid is reported.

To demonstrate the advantages of the anticorrosion activity of additives of this invention, various additives were added to a fluid designated as Fluid A. Fluid A was a mixture consisting, by weight, of about 50% of m-bis (phenylmercapt)benzene, about 25% of mphenoxyphenyl m-phenylmercaptophenyl sulfide, about 11% of bis(m-phenoxyphenyl)sulfide and about 14% of bis(mphenylmercaptophenyl)sulfide. Table 1 below presents the data obtained by employing 0.1%, by weight, of each ad- 14 tained with different amounts of S-aminoindazole employed in other fluids. The fluid designated Fluid B in Table III is a mixture consisting, by weight, of about 50% of m-phenoxyphenyl m-phenylmercaptophenyl sulfide, about 22% of his (phenoxyphenyl)sulfide and about 28% of his (m-phenylmercaptophenyl)sulfide. The concentration of the additive is given in weight percent of the fluid and the copper attack is reported as weight change in milligrams per unit of surface area in contact with the fluid.

ditive in Fluid A when the composition was subjeced to the above-described test. TABLE III TABLE I Additive concentra- Copper Metal weight change, tion wt. attack, mg. 0111. Base stock percent rug/cm. Additive Copper Silver Pentgerythrltol tetraoctanoate 18 g. 5(1) 0 None, control (average of 23 tests) -2. 39 67 Bis(phenylmercapto)benzene 0 3. 3 B-nminoindazole -.01 -,39 Dow, .025 0. 90 fi-aminoindazole 01 23 Do 05 +0. 10 7-aminoindazole 0O Do 20 0. 02 3-amino-1,2,4-trlazole .09 -.56 2O FluldB 0 2.80 3,5-diamino-1,2,4-triazole 03 13 Do 025 0. 96 5amino-l carbamyl-3-pyrazoleacetie acid.- 01 10 Do 05 22 2,4-dicyano-S-ethyH-methyl glutaramide, 57 59 Do 10 +0. 14 4-amlno-1,8-naphthallmide 35 .53 2,2-octamethylene dl-2-irnidazoline 04 -.31 i i i i i Y'Ecii 'iifiiidi" iii am no- -vr azo 0- py ne 22 mmmmmod,2,6'8 tetmamd0mme 25 In accordance with the above data, it is evident that B-aminoindole -1.o4 16 some of the fluids, particularly thioethers and mixtures of 5.hydroxyindole l. 27 27 ,gyadiaminoaarbaml" thioethers, when used as lubricants for gas turbine en 34-diiamlixiglolgrrlidinefi -.05 ,1 gines are outstanding with respect to high temperiturg 2-am no co cac .37 .39 7amino-s-triazolo(1,5-a)-pyrimidin-5-(4H)one--. .44 .35 Stfqbhty p cqmpwblhty l i me 4-niethyl-1H-pyrazole(3,4-b)-pyridine-3,6-dio1. -,22 with additives of this invention. Thus, this invention re- Pammopymmh(3,44Wyflm1d1n6 late to a novel method of lubricating gas turbine en- 4,5-diamiiiopyiiinidine -.39 -.53 d 2,4,5 tr1am1n0pyrhn1d1ne gines which comprises maintaining on the bearings an 341mlnol-phenyl-2-pyrazolin-5-one 1.41 .52 n i a l b i ti o nt 2-eyano amino-4,fi-dihydroxypyrlmldine .194 .29 other pomts Wear e e h fl t 4,6.d1hydmxypyfl(m1d,)m Elia --1,2% of a composition of 1118 invention. Otf elr ui s contain- Mmlnopyflmido PW or in an additive of t is invention use u as as tur ine 3,5,7-triainino-s-triazolo(4,3-a)-s-trlazlne.. -.69 .25 l b t t 1 1 1 t g f C 5-hydroxy-7-methyl-1,3,8-triazaindo1izine.- -1.64 .43 engine rlcajn S are p y P0 Y0 35 0 2-18 fi-hydroxyindozolel fatty acids, mixtures of neopentyl polyol esters of C 1 .05% concentration.

The data in Table I is to be compared with data presented in Table II below. The data in Table II was obtained from additional runs of the same test employing Fluid A containing 0.1% by weight of additives of very similar molecular structure to those listed in Table I.

TABLE II Metal weight change,

lug/cm.

Additive Copper Silver Control, from above 2. 39 67 fi-amlnouracil 2. 6 74 B-aminouraeil 3. 1 48 2,7-dimercapto-4-hydroxypyrimido-(4,543)- pyrimidine 5. 4 81 Benzimidazole 3. 7 --1. 2 2-phenyl-4,6-bis(3-a.m1nophenyl)-1,3,6-triazine 2. 8 07 2-inercaptopyrimidine 4. 4 1. 5 4,6-dlhydroxy-Z-mercaptopyrimidine. 6. 2 l. 1 4-amin0'6-hydroxy-2-mercaptopyrimidine 6. 2 93 Z-amino-4,6-dihydroxypyrimidine 3. 4 61 1-[3-(6-chloropyridazinyl)]-3-(3,4-dichlorophenyl) urea 6. 9 1. 7 3-methyl-5-phenyl pyrazole 8. 4 2. 0 2hydroxy-3,3-4,4,5,6,hexaehlorocarbanilide.. 8. 8 3. 1 (3, i-dichlorophenylureldo)p-menthane 3. 0 69 5-nitroindazole 8. 4 l. 4

A comparison of the results obtained in Tables I and II above indicates the selectivity required in solving the problem of metal corrosion by functional fluids at high temperatures by the incorporation of additives. Many additives which because of their structural similarity would be expected to reduce metal attack are found to increase it under the high temperature conditions for which the compositions ofthis invention are particularly useful.

In Table III below the results obtained using the abovedescribed test are presented wherein fluids are employed containing S-aminoindazole, one of the preferred additives of this invention. Also included are the results obfatty acids, dipentaerythritol ester of C fatty acids and mixtures of the pentaerythritol esters and dipentaerythritol esters. Especially useful as gas turbine engine lubricants are mixtures of polyphenyl ethers and polyphenyl thioethers containing corrosion reducing amounts of an additive of this invention.

As a result of the excellent physical properties of the compositions particularly described above, improved bydraulic pressure devices can be prepared in accordance with this invention which comprise in combination a fluid chamber and an actuating fluid in said chamber, said fluid comprising a mixture of one or more of the base stocks hereinbefore described. In such a hydraulic apparatus wherein a movable member is actuated by the above-described functional fluids, performance characteristics are obtainable which are superior to those heretoiore obtainable.

Because of the excellent fire-resistance of the compositions of this invention, their exceptionally low pour points, and good lubricity, the functional fluids of this invention can be utilized in those hydraulic systems wherein power must be transmitted and the frictional parts of the system lubricated by the hydraulic fluid utilized. Thus, the novel composition of this invention finds utility in the transmission of power in a hydraulic system having a pump therein supplying the power for the system. In such a system, the parts which are so lubricated include the frictional surfaces of the source of power, namely the pump, valves, operating pistons and cylinders, fluid motors and in some cases, for machine tools, the ways, table and slides. The hydraulic system may be of either the constant-volume or the variable-volume type of system.

The pumps may be of various types, including the piston-type pump, more particularly the variable-stroke piston pump, the variable-discharge or variable displacement piston pump, radical-piston pump, axial-piston pump, in which a pivoted cylinder block is adjusted at various angles with the piston assembly, for example,

the Vickers axial-piston pump, or in which the mechanism which drives the pistons is set at an angle adjustable with the cylinder block; gear-type pump, which may be spur, helical or herringbone gears, variations of internal gears, or a screw pump; or vane pumps. The valves may be stop valves, reversing valves, pilot valves, throttling valves, sequence valves or relief valves. Fluid motors are usually constantor variable-discharge piston pumps caused to rotate by the pressure of the hydraulic fluid of the system with the power supplied by the pump power source. Such a hydraulic motor may be used in connection with a variable-discharge pump to form a variable-speed transmission.

Although the compositions described above are generally quite suitable for most applications, it may also be desirable to add small amounts of various other functional addition agents such as viscosity index improvers, e.g., a polymerized methacrylate ester, an alkylated polystyrene, or the polyether condensation products of ethylene oxide or propylene oxide, or both, with a glycol such as ethylene glycol, propylene glycol, butanediol, etc., or with an aliphatic alcohol such as butanol, oetanol, decanol, tridecanol, etc., pour point depressants, oxidation inhibitors, detergents, corrosionand rust-inhibiting agents, anti-wear and lubricity agents, anti-foaming agents such as the silicone polymers, and the like.

While this invention has ben described with respect to various specific examples and embodiments, it is to be understood that the invention is not limited thereto and that it can be variously practiced within the scope of the following claims.

The embodiments of this invention in which a particular property or privilege is claimed are defined as follows:

1. Composition comprising (I) a major amount of a fluid of lubricating or hydraulic viscosity selected from the group consisting of:

( i) polyphenyl thioethers,

(ii) mixed polyphenyl oxy-thioethers, and

(iii) admixtures thereof, and

16 (II) a corrosion inhibiting amount of a pyrimidine of the formula Rl (IV) wherein R is hydrogen, cyanoamino, NH or OH and R R and R are hydrogen, amino or OH.

2. Composition of claim 1 wherein R and R are amino.

3. Composition of claim 1 wherein R and R are amino.

4. Composition of claim 1 wherein R, R and R are amino.

5. Composition of claim 1 wherein R is cyanoamino.

6. Composition of claim 1 wherein R and R are bydroxyl.

7. Composition of claim 1 wherein the pyrimidine of iv is 4,5-diaminopyrimidine.

8. Composition of claim 1 wherein the pyrimidine of iv is 2,4,S-triaminopyrimidine.

9. Composition of claim 1 wherein the pyrimidine of iv is 2-cyano amino-4,6-dihydroxy-pyrimidine.

10. Composition of claim 1 wherein the pyrimidine of iv is 4,6-dihydroxypyrimidine.

References Cited UNITED STATES PATENTS 2,160,293 5/1939 Shoemaker et a1. 2525l.5 R 2,197,834 4/1940 Reiff et a] 252-35 FOREIGN PATENTS 851,651 10/1960 Great Britain 25252 R DANIEL E. WYMAN, Primary Examiner W. H. CANNON, Assistant Examiner US. Cl. X.R.

zg g UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION Patent No, 3,759,829 Dated September 18, 1973 Inventor(s) James D. Sullivan It is certified that error appears in the above-identified patent and that said Letters Patent are hereby corrected as shown below:

Column.3, line 37, the formula should be corrected to read:

N N c R R I H .\N/C\N /N Column 3, line H8, "aninocarbazols" should read Column 7, line H2, "noxy)benzene" should read "noxyphenoxy)benzene".

Column 15, line 27, "ben" should read "been".

Signed and sealed this 9th day of April 197A.

(SEAL) Attest:

c MARSHALL 13mm Commissioner of Patents EDWARD M .lETCHER JR Attesting Officer +22% UNITEDISTATES PATENT OFFICE CERTIFICATE OF CORRECTION Patent No. 3 ,759 ,829 Dated September 18 1973 Inventot(s) James D-. Sullivan It is certified that error appears in the above-identified patent and that said Letters Patent are hereby corrected as shown below:

r Column .3, line 37, the formula should be corrected to read: I

/C R N N C R R l {I I Column 3, line +8, "aninocarbazols" should read "aminocarbazols".

Column 6 line 57 "m" should read "5" Column 7, line +2, "noxy)benzene" should read "noxyphenoxy)benzene".

Column 15, line 27, "ben" should read "been".

Signed and sealed this 9th day of April 197L (SEAL) Attest:

EDI-JARD MELETSHTJRJR. C MARSHALL DANN I Attesting Officer Commissionerof Patents