EP0871690A1 - Hydraulic fluids for use in aircraft - Google Patents
Hydraulic fluids for use in aircraftInfo
- Publication number
- EP0871690A1 EP0871690A1 EP95944797A EP95944797A EP0871690A1 EP 0871690 A1 EP0871690 A1 EP 0871690A1 EP 95944797 A EP95944797 A EP 95944797A EP 95944797 A EP95944797 A EP 95944797A EP 0871690 A1 EP0871690 A1 EP 0871690A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- hydraulic fluid
- phosphate
- group
- alkyl
- carbon atoms
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M169/00—Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
- C10M169/04—Mixtures of base-materials and additives
- C10M169/044—Mixtures of base-materials and additives the additives being a mixture of non-macromolecular and macromolecular compounds
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- C10M105/00—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
- C10M105/74—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing phosphorus
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- C10M107/00—Lubricating compositions characterised by the base-material being a macromolecular compound
- C10M107/20—Lubricating compositions characterised by the base-material being a macromolecular compound containing oxygen
- C10M107/30—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M107/32—Condensation polymers of aldehydes or ketones; Polyesters; Polyethers
- C10M107/34—Polyoxyalkylenes
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- C10M129/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
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- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/08—Hydraulic fluids, e.g. brake-fluids
Definitions
- This invention relates to novel hydraulic fluids containing a specific combination of components which combination imparts beneficial properties to the fluid, particularly when used as aircraft hydraulic fluids.
- Hydraulic fluids including those based on organic phosphate esters, are well known in the art and have been recognized for quite some time as advantageous for use in aircraft where they operate as a power transmission medium.
- the aircraft hydraulic fluid is conventionally formulated to include additives such as viscosity index improvers, anti-erosion agents, acid scavengers, anti- oxidants, rust inhibitors and the like so that the composition meets the needs of modem aircraft.
- One problem typically encountered with aircraft hydraulic fluids is that combinations of additives in a particular basestock do not always provide for the desired or expected combination of properties. For example, a combination of additives in one basestock may not perform nearly as well as in another basestock. Also, the inclusion of an additional additive into a hydraulic fluid formulation can deleteriously affect the performance of one or more of the additives already employed in that formulation.
- the art has typically assigned some sort of incompatibility of the basestock with one or more of the additives employed in conjunction therewith or incompatibility of one additive with one or more of the other additives used in the formulation in order to explain this phenomena.
- suitable aircraft hydraulic fluids is an empirical exercise and the formulator typically is required to balance the properties of the formulation against the particular additives and basestocks employed.
- Particular problems of concern to the formulator include the inclusion of suitable acid scavengers, anti-erosion agents and viscosity index improvers in the aircraft hydraulic formulation.
- aircraft hydraulic fluids commonly become contaminated with moisture. Water enters the hydraulic system with air bled from an engine compressor stage. During operation, the moisture level in the fluid can typically range from about 0.1 to about 0.5 weight percent. Water causes hydrolytic decomposition of phosphate esters to produce partial esters of phosphoric acid which can cause corrosion.
- an anti-erosion agent is incorporated into the aircraft hydraulic fluid to counteract erosive conditions typically occurring in the power transmission mechanisms of the aircraft.
- Erosion is a form of electrochemical corrosion, more precisely referred to as zeta corrosion. The process of erosion results in the wearing of the metering edges of the hydraulic valves leading to degraded performance of the hydraulic systems. Erosion can also lead to metal contaminants, in ionic form, which reduce the oxidative stability of the fluid thereby accelerating corrosion and catalytically accelerating the decomposition of the phosphate ester basestock.
- Viscosity index improvers are employed to limit the effect of temperature on the viscosity of the hydraulic fluid composition. Specifically, while viscosity control at both elevated and reduced temperatures is essential for the hydraulic fluid, it is critically important that viscosity control be maintained at reduced temperatures typically encountered during flights at high altitudes.
- This invention overcomes the problems of the prior art by providing for an aircraft hydraulic fluid comprising a novel combination of additives and organic phosphate basestocks which provides excellent results in scavenging acid generated by the partial esters of phosphoric acid, in controlling erosion at the metering edges of the hydraulic servo valves, in reducing electrodeposited solids and in maintaining suitable viscosity over a wide range of temperatures.
- the formulation discovered by this invention comprises: a basestock combination of from about 60 to 95 weight percent of a trialkyl phosphate and from about 5 to about 40 weight percent of a second component selected from the group consisting of a triaryl phosphate, a mixture of a triaryl phosphate and a linear polyoxyalkylene material, and a linear polyoxyalkylene material which basestock is free of dialkyl aryl phosphate and alkyl diaryl phosphate, an acid scavenger of the formula
- R is selected from the group consisting of an alkyl group of from 1 to 10 carbon atoms optionally containing from 1 to 4 ether oxygen atoms therein and cycloalkyl of from 3 to 10 carbon atoms
- each R' is independently selected from the group consisting of hydrogen, alkyl of from 1 to 10 carbon atoms and -C(O)OR" where R" is alkyl of from 1 to 10 carbon atoms optionally containing from 1 to 4 ether oxygen atoms therein or cycloalkyl of from 3 to 10 carbon atoms
- R"' is selected from the group consisting of hydrogen, alkyl of from 1 to 10 carbon atoms and -C(O)OR" where R" is alkyl of from 1 to 10 carbon atoms optionally containing from 1 to 4 ether oxygen atoms therein or cycloalkyl of from 3 to 10 carbon atoms
- an anti-erosion agent which is a salt of perfluoroalkyl or perfluorocycloal
- a phosphate basestock comprising a mixture of triaryl phosphate and trialkyl phosphate in aircraft hydraulic fluids
- U.S. Patent No. 5,035,824 the use of alkali (e.g., potassium) perfluoroalkyl or perfluorocycloalkyl sulfonate as an anti- erosion agent in aircraft hydraulic fluids is disclosed in U.S. Patent No. 3,679,587; and the use of certain epoxides of the formula described above in aircraft hydraulic fluids is disclosed in U.S. Patent No. 3,723,320.
- hydraulic fluids used in aircraft and sold under the trademark Skydrol ® by Monsanto Company are believed to comprise a basestock having trialkyl phosphate, dialkyl aryl phosphate and alkyl diaryl phosphate components with little or no triaryl phosphate as well as potassium perfluorocyclohexyl sulfonate and the monoepoxide 7-oxabicyclo[4.1.0]heptane-3-carboxylic acid, 2- ethylhexyl ester.
- This invention is directed to an aircraft hydraulic fluid comprising a novel combination of additives and organic phosphate basestocks which provides excellent results in scavenging acid generated by the partial esters of phosphoric acid, in controlling erosion in the formulation, and in reducing electrodeposited solids. These results are particularly surprising because rather than being incompatible, the additives and basestock employed in the formulation described herein are, in fact, synergistic. Specifically, in one of its composition aspects, this invention is directed to an aircraft hydraulic fluid comprising
- R 4 and R 6 are independently selected from the group consisting of hydrogen and hydrocarbyl groups of from 1 to about 30 carbon atoms, R 5 is selected from the group consisting of hydrogen and methyl, and n is an integer such that the number average molecular weight of the polymer is from about 300 to about 1000;
- R is selected from the group consisting of an alkyl group of from 1 to 10 carbon atoms optionally containing from 1 to 4 ether oxygen atoms therein and cycloalkyl of from 3 to 10 carbon atoms
- each R' is independently selected from the group consisting of hydrogen, alkyl of from 1 to 10 carbon atoms and -C(O)OR" where R" is alkyl of from 1 to 10 carbon atoms optionally containing from 1 to 4 ether oxygen atoms therein or cycloalkyl of from 3 to 10 carbon atoms
- R"' is selected from the group consisting of hydrogen, alkyl of from 1 to 10 carbons atoms and -C(O)OR" where R" is alkyl of from 1 to 10 carbon atoms optionally containing from 1 to 4 ether oxygen atoms therein or cycloalkyl of from 3 to 10 carbon atoms
- the acid scavenger is selected from the group consisting of 7-oxabicyclo[4.1.0]heptane-3-carboxylic acid, 2- ethylhexyl ester and 7-oxabicyclo[4.1.0]heptane-3,4-dicarboxylic acid, di(wo-butyl) ester.
- the aircraft hydraulic fluid described above further comprises
- this invention is directed to an aircraft hydraulic fluid comprising
- a viscosity index improver effective in reducing the effect of temperature on viscosity on the fluid by providing for a hydraulic fluid composition containing the VI improver which has a viscosity of from about 3 to about 4 cSt at 210°F, a viscosity of from about 9 to about 12.5 cSt at 100°F, and a viscosity of less than about 2000 cSt at -65 °F, with the proviso that the viscosity index improver is not a poly(alkyl acrylate) ester wherein the hydraulic fluid is free of dialkyl aryl phosphate and alkyl diaryl phosphate components.
- the aircraft hydraulic fluid described above further comprises from about 0.1 to about 4 weight percent, based on the total weight of the hydraulic fluid, of a trialkyl phosphate wherein each alkyl group of the trialkyl phosphate is independently a straight or branched chain alkyl group of from 1 to 3 carbon atoms.
- this invention is directed to an aircraft hydraulic fluid comprising (a) from about 60 to 90 weight percent, based on the total weight of the fluid, of tributyl phosphate, and from about 5 to 30 weight percent, based on the total weight of the fluid, of a second component selected from the group consisting of triaryl phosphate, a mixture of triaryl phosphate and a linear polyoxyalkylene material, and a linear polyoxyalkylene material which basestock is free of dialkyl aryl phosphate and alkyl diaryl phosphate wherein each of the aryl groups of the triarylphosphate is independently phenyl or alkyl substituted phenyl having from 7 to 20 carbon atoms and still further wherein the linear polyoxyalkylene material is of the formula
- R 4 and R 6 are independently selected from the group consisting of hydrogen and hydrocarbyl groups of from 1 to about 30 carbon atoms, R s is selected from the group consisting of hydrogen and methyl, and n is an integer such that the number average molecular weight of the polymer is from about 300 to about 1000;
- a viscosity index improver effective in reducing the effect of temperature on viscosity on the fluid by providing for a hydraulic fluid composition containing the VI improver which has a viscosity of from about 3 to about 4 cSt at 210°F, a viscosity of from about 9 to about 12.5 cSt at 100°F, and a viscosity of less than about 2000 cSt at -65 °F, with the proviso that the viscosity index improver is not a poly (alkyl acrylate) ester wherein the hydraulic fluid is free of dialkyl aryl phosphate and alkyl diaryl phosphate components.
- the basestock composition employs from about 8 to about 25 weight percent, based on the weight of the basestock, of a linear polyoxypropylene or polyoxyethylene material.
- the rust inhibitor comprises an overbased calcium or potassium phenate or a sulfurized calcium or potassium phenate.
- this invention is directed to a method for reducing electrodeposited solids during operation of an aircraft hydraulic system which method comprises:
- This invention is directed to aircraft hydraulic fluid compositions comprising a specific combination of an organic phosphate ester basestock, an acid scavenging agent, an anti-erosion agent and a viscosity index improver.
- the compositions described herein are conventionally prepared by blending the components of the composition together until homogeneous.
- the blending process may be conducted as a single step process where all of the components are combined and then blended or may be conducted as a multi-step process where two or more of the components are combined and blended and additional components are added to the blended mixture and the resulting mixture further blended.
- the hydraulic fluid composition of this invention comprises, in one embodiment, from about 60 to about 90 weight percent, based on the total weight of the composition, of an organic phosphate ester basestock.
- This basestock comprises from about 60 to 95 weight percent, based on the total weight of the basestock, of a trialkyl phosphate and from about 5 to about 40 weight percent, based on the total weight of the basestock, of a second component selected from the group consisting of triaryl phosphate, a mixture of triaryl phosphate and a linear polyoxyalkylene material, and a linear polyoxyalkylene material.
- the basestock is further characterized as being free of dialkyl aryl phosphate and alkyl diaryl phosphate.
- the hydraulic fluid composition of this invention comprises from about 60 to 90 weight percent, based on the total weight of the fluid composition, of tributyl phosphate, and from about 5 to 30 weight percent, based on the total weight of the fluid composition, of a second component selected from the group consisting of triaryl phosphate, a mixture of triaryl phosphate and a linear polyoxyalkylene material, and a linear polyoxyalkylene material which basestock is free of dialkyl aryl phosphate and alkyl diaryl phosphate.
- the phosphate esters can be represented by the formula:
- each of R 1 , R 2 and R 3 is independently an alkyl group of from 1 to 12 carbon atoms.
- each of R 1 , R 2 , and R 3 is independently phenyl or alkyl substituted phenyl having from 7 to 20 carbon atoms.
- the alkyl groups of the trialkyl phosphates include aliphatic and alicyclic groups where the aliphatic groups include straight and branched alkyl groups.
- trialkyl phosphate esters include, by way of example, tri-n-butyl phosphate, tri(wo-butyl) phosphate, tri(jec-butyl) phosphate, di(wo-butyl) pentyl phosphate, tri(n-pentyl) phosphate, tri-2- ethylhexyl phosphate, and the like.
- Preferred trialkyl phosphates include the tributyl phosphates recited above.
- trialkyl phosphates can be used.
- Preferred mixtures of trialkyl phosphates include mixtures of tri(wo-butyl) phosphate and tri(n- butyl) phosphate in a ratio of about 1: 1 to about 10:1, more preferably in a ratio of about 2: 1 to about 3: 1.
- the alkyl substituted phenyl groups of the triaryl phosphates include phenyl groups having from 1 to 3 alkyl substituents wherein the alkyl groups are straight or branched chain groups of from 1 to 14 carbon atoms and further wherein each alkyl substituted phenyl group has a maximum of up to 20 carbon atoms.
- Examples of triaryl phosphate esters include, by way of example, tri(i5 ⁇ -propylphenyl) phosphate, tri(butylated phenyl) phosphate, tricresyl phosphate, and the like. Mixtures of triaryl phosphate can be used.
- trialkyl phosphates and triaryl phosphates include a mixture of tributyl phosphate and tri(wo-propylphenyl) phosphate at about a 6: 1 to 8: 1 ratio, preferably at about a 6: 1 to 7: 1 ratio (e.g., 6.7: 1); and a mixture of tributyl phosphate and tri(butylated phenyl) phosphate at about a 6: 1 to 7: 1 ratio (e.g., 6.3: 1).
- the organic phosphate ester base stock further comprises from about 0.1 to about 4 weight percent, more preferably from about 1 to 2 weight percent, based on the total weight of the hydraulic fluid, of a trialkyl phosphate wherein each alkyl group of the trialkyl phosphate is independently a straight or branched chain alkyl group of from 1 to 3 carbon atoms.
- a trialkyl phosphate or a mixture of such trialkyl phosphates in the organic phosphate ester base stock composition described herein provides for reduced viscosity of the hydraulic fluid at low temperatures without causing undesirable swelling of ethylene propylene seals.
- Preferred trialkyl phosphates useful for this purpose include trimethyl phosphate, triethyl phosphate, tri(n-propyl) phosphate and tri(w ⁇ - propyl) phosphate.
- R 4 and R 6 are independently selected from the group consisting of hydrogen and hydrocarbyl groups of from 1 to about 30 carbon atoms
- R 5 is selected from the group consisting of hydrogen and methyl
- n is an integer such that the number average molecular weight of the polymer is from about 300 to about 1000.
- Such materials are either commercially available or can be prepared by methods known per se in the art. See, for example, U.S. Patent No. 4,933,485 which is incorporated herein by reference in its entirety.
- the inclusion of such linear polyoxypropylene or polyoxyethylene material in the organic phosphate ester basestock composition synergistically provides for enhanced hydrolytic stability. Additionally, the composition provides for significantly reduced titanium weight loss and hydrogen incorporation which leads to increased resistance to titanium embrittlement in high temperature exposure tests.
- the term "hydrocarbyl” denotes an organic radical composed of carbon and hydrogen which may be aliphatic, alicyclic, aromatic or combinations thereof (e.g., arylalkyl).
- the hydrocarbyl group will be relatively free of aliphatic unsaturation, i.e., ethylene and acetylenic unsaturation, particularly acetylenic unsaturation.
- the aircraft hydraulic fluid composition of this invention comprises an acid scavenger of the formula
- R is selected from the group consisting of an alkyl group of from 1 to 10 carbon atoms optionally containing from 1 to 4 ether oxygen atoms therein and cycloalkyl of from 3 to 10 carbon atoms
- each R' is independently selected from the group consisting of hydrogen, alkyl of from 1 to 10 carbon atoms and -C(O)OR" where R" is alkyl of from 1 to 10 carbon atoms optionally containing from 1 to 4 ether oxygen atoms therein or cycloalkyl of from 3 to 10 carbon atoms
- R" ' is selected from the group consisting of hydrogen, alkyl of from 1 to 10 carbons atoms and -C(O)OR" where R" is alkyl of from 1 to 10 carbon atoms optionally containing from 1 to 4 ether oxygen atoms therein or cycloalkyl of from 3 to 10 carbon atoms.
- Preferred acid scavengers of the above formula are the monoepoxide 7-oxabicyclo[4.1.0]heptane-3-carboxylic acid, 2-ethylhexyl ester which is disclosed in U.S. Patent No. 3,723,320, and the. onoepoxide 7-oxa- bicyclo[4.1.0]-heptane-3,4-dicarboxylic acid, dialkyl esters [e.g., the di(iso- butyl) ester]. Dialkyl esters of this monoepoxide are also disclosed in U.S. Patent No. 3,723,320.
- the trialkyl and tetraalkyl esters are prepared via conventional Diels-Alder reaction procedures via a suitable unsaturated trialkyl or tetraalkyl ester and a suitable 1,3-diene.
- the Diels-Alder reaction provides for 4 + 2 cycloaddition to provide for a cyclohexene derivative having the suitable trialkyl or tetraalkyl esters.
- the unsaturation in the cyclohexene is utilized to provide for epoxide formation via conventional methods.
- Suitable unsaturated trialkyl and tetraalkyl esters are known in the art.
- tetraethyl ethylene tetracarboxylate is available from Fluka (Ronkonoma, NY).
- the alkyl groups of this tetraethyl ester can readily be exchanged via conventional techniques to provide for other esters as defined above.
- this invention is directed to a method for reducing the swelling of ethylene propylene seals in an aircraft hydraulic system due to contact of said seals with an aircraft hydraulic fluid composition containing 7-oxabicyclo-[4.1.0]heptane-3- carboxylic acid, 2-ethylhexyl ester as the acid scavenger which method comprises:
- R is selected from the group consisting of an alkyl group of from 1 to 10 carbon atoms optionally containing from 1 to 4 ether oxygen atoms therein and cycloalkyl of from 3 to 10 carbon atoms
- each R"' is independently selected from the group consisting of hydrogen, alkyl of from 1 to 10 carbons atoms and -C(O)OR where R is as defined above, with the proviso that at least one of R"' is -C(O)OR, and
- 2-ethylhexyl ester acid scavenger is replaced by the diester acid scavenger described above.
- the acid scavenger whether as the mono-, di-, tri-, or tetraester, is employed in an amount effective in scavenging the acid generated as partial esters of phosphoric acid during operation of the power transmission mechanisms of an aircraft and is preferably employed at from about 4 to about 10 weight percent, based on the total weight of the hydraulic fluid composition and more preferably from about 5 to about 9 weight percent and still more preferably from about 6 to about 8 weight percent.
- the aircraft hydraulic fluid composition described herein comprises as the anti-erosion agent an alkali metal salt, and preferably the potassium salt, of perfluoroalkyl or perfluorocycloalkyl sulfonate which are disclosed in U.S. Patent No. 3,679,587.
- perfluoroalkyl and perfluorocyclo- alkyl sulfonates preferably encompass alkyl groups of from 1 to 10 carbon atoms and cycloalkyl groups of from 3 to 10 carbon atoms.
- the anti- erosion agent is employed in an amount effective to inhibit erosion in the power transmission mechanisms of an aircraft and, preferably, is employed in an amount of from about 0.01 to about 0.1 weight percent, based on the total weight of the hydraulic fluid composition and more preferably from about 0.025 to about 0.075 weight percent. Mixtures of such anti-erosion agents can be used.
- Viscosity Index Improver The hydraulic fluid composition described herein contains a polymeric viscosity index (VI) improver to limit the effect of temperature on viscosity.
- VI improvers are either non-dispersant or dispersant VI improvers which are well known in the art.
- Preferred VI improvers include poly(alkyl methacrylate) esters of the type disclosed in U.S. Patent No. 3,718,596 which are commercially available from Rohm & Haas, Spring House, PA. Such esters typically having a molecular weight range of from about 50,000 to about 1,500,000 and preferably from about 50,000 to 250,000.
- VI improvers include those having a molecular weight peak at about 70,000 to 100,000 (e.g., about 85,000 or 90,000 to 100,000).
- a preferred VI improver is a poly(alkyl methacrylate) ester sold under the tradename PA 7570 by Rohm & Haas. Mixtures of VI improvers can also be used.
- VI improver is employed in the hydraulic fluids described herein to reduce the effect of temperature on the viscosity of the fluid.
- VI improvers suitable for use herein are those which reduces the effect of temperature on viscosity of the fluid by providing for a hydraulic fluid composition containing the VI improver which has a viscosity of from about 3 to about 4 cSt at 210°F, a viscosity of from about 9 to about 12.5 cSt at 100°F, and a viscosity of less than about 2000 cSt at -65 °F. This last property is particularly significant since at high elevations extremely low temperatures are encountered and, accordingly, OEM specifications require a viscosity of less than 2000 cST at -65 °F.
- poly(alkyl acrylate) esters such as those described in U.S. Patent No. 3,718,596, typically fail to adequately reduce the effect of temperature on viscosity when used in the hydraulic fluids described herein.
- hydraulic fluid compositions formulated with a poly (alkyl acrylate) ester generally have an unacceptably high viscosity at low temperatures (e.g., a viscosity greater than 2000 cSt at -65 °F).
- still other viscosity index improvers also fail to provide adequate viscosity at low temperatures.
- a test to determine the usefulness of a candidate VI improver in the compositions described herein can be conducted simply by measuring the viscosity of the hydraulic fluid composition comprising this candidate VI improver in ASTM test D445 at several different temperatures (i.e. , -65°F, 100°F and 210°F).
- the VI improver is employed in an amount effective to reduce the effect of temperature on viscosity, preferably from about 1 to about 8 weight percent, more preferably from about 2 to about 8 weight percent, and still more preferably from about 3 to about 5 weight percent based on the total weight of the hydraulic fluid composition.
- the VI improver is formulated with a portion of the trialkyl phosphate basestock, typically as a 1: 1 mixture.
- the hydraulic fluid composition described herein contains a conventional anti-oxidant or mixture of anti- oxidants ("anti-oxidant").
- anti-oxidants include phenolic anti- oxidants, such as 2,6-di-tertiary-butyl-/?-cresol and tetrakis [methylene (3,5- di-t-butyl-4-hydroxyhydrocinnamate)] methane sold under the tradename Irganox ® 1010 (Ciba-Geigy); amine anti-oxidants, including diarylamines such as phenyl- ⁇ -naphthylamine or alkylphenyl- ⁇ -naphthylamine, or the reaction product of N-phenylbenzylamine with 2,4,4-trimethylpentene sold under the tradename Irganox ® L-57 (Ciba-Geigy), diphenylamine, di(octylphenyl)
- anti-oxidants include aminophenols such as N-butylaminophenol, N-methyl-N- amylaminophenol and N-wo-octyl- -aminophenol as well as mixtures of any such conventional anti-oxidants.
- a preferred mixture of such anti-oxidants being 2,6-di-tertiary- butyl-/>-cresol and di(octylphenyl)amine (e.g., a 1 : 1 mixture).
- Another preferred mixture of anti-oxidants is 2,6-di-tertiary-butyl-/?-cresol, di(octylphenyl)amine and 6-methyl-2,4-bis[(octylthio)-methyl]-phenol (e.g. , a 1:2:4 mixture) which mixture is particularly useful with basestocks comprising tri(wo-butyl) phosphate.
- Still another preferred mixture of anti- oxidants is 2,6-di-t-butyl-p-cresol, di(octylphenyl)amine and tetrakis
- the anti-oxidant is employed in an amount effective to inhibit oxidation of the hydraulic fluid, preferably, from about 0.5 to about 3 weight percent, more preferably from about 0.5 to 2 weight percent and still more preferably at about 1.25 to 1.75 weight percent based on the total weight of the hydraulic fluid composition.
- the hydraulic fluid compositions described herein contain a rust inhibitor.
- Suitable rust inhibitors include, by way of example only, calcium dinonylnaphthalene sulfonate, a Group I or Group II metal overbased and/or sulfurized phenate, and a compound of the formula set forth below:
- R 7 is selected from the group consisting of alkyl of from 1 to 40 carbon atoms, alkenyl of from 3 to 40 carbon atoms, -COOR 8 and -CH 2 CH 2 N[CH,CH(R 9 )OH] 2 where R 8 is alkyl of from 1 to 40 carbon atoms, and wherein each R 9 is independently selected from the group consisting of hydrogen and methyl, including N,N,N',N' tetrakis (2- hydroxypropyl) ethylene diamine and N,N-bis(2-hydroxyethyl)tallowamine sold under the tradename Ethomeen ® T/12, mixtures of such inhibitors, and the like.
- alkenyl refers to a straight or branched chain aliphatic radical having one or more olef ⁇ nic double bonds, such as an oleyl group.
- the Group I and Group II metal overbased and/or sulfurized phenates preferably are either sulfurized Group I or Group II metal phenates (without CO 2 added) having a Total Base Number (TBN) of from greater than 0 to about 200 or a Group I or Group II metal overbased sulfurized phenate having a TBN of from 75 to 400 prepared by the addition of carbon dioxide during the preparation of the phenate. More preferably, the metal phenate is a potassium or calcium phenate. Additionally, the phenate advantageously modifies the pH to provide enhanced hydrolytic stability.
- Each of these components are either commercially available or can be prepared by art recognized methods.
- Group II metal overbased sulfurized phenates are commercially available from Chevron Chemical Company, San Ramon, California under the tradename OLOA ® including, OLOA 219 ® , OLOA 216Q ® and the like and are described by Campbell, U.S. Patent No. 5,318,710, and by MacKinnon, U.S. Patent No. 4,206,067.
- OLOA ® including, OLOA 219 ® , OLOA 216Q ® and the like and are described by Campbell, U.S. Patent No. 5,318,710, and by MacKinnon, U.S. Patent No. 4,206,067.
- N,N,N',N' tetrakis (2-hydroxy-propyl) ethylene diamine is disclosed by MacKinnon, U.S. Patent No. 4,324,674. The disclosures of each of these patents is incorporated herein in their entirety.
- the rust inhibitor is employed in an amount effective to inhibit the formation of rust, preferably from about 0.001 to about 1 weight percent, more preferably about 0.01 to about 0.5 weight percent, and still more preferably at about 0.02 to about 0.1 weight percent based on the total weight of the hydraulic fluid composition.
- the rust inhibitor comprises a mixture of N,N,N',N' tetrakis (2-hydroxypropyl) ethylene diamine and a Group II metal overbased phenate (e.g. , a 5: 1 mixture).
- the rust inhibitor comprises a mixture of N,N-bis(2-hydroxyethyl)tallowamine (Ethomeen ® T/12) and a Group II metal overbased sulfurized phenate (e.g., a 5:1 mixture).
- the hydraulic fluid composition described herein can optionally contain further conventional additives such as copper corrosion inhibitors, anti-foaming agents, dyes, etc.
- Example 1 The purpose of this example is to demonstrate that the components employed in the compositions of this invention are compatible and synergistic with each other as evidenced by the performance characteristics of the hydraulic fluid. Specifically, Formulation 1 , a formulation of this invention, was prepared by blending the following components: FORMULATION 1
- VI improver 2 8.7% anti-oxidant 3 1.5% rust inhibitor 4 0.06%
- Example 2 The purpose of this example is to demonstrate that different viscosity index improvers do not reduce the effect of temperature on the viscosity of hydraulic fluids because at 210°F, these compositions provided acceptable viscosities only at unacceptable concentrations of VI improvers. Specifically, three different VI improvers were used at different concentrations to determine the suitability of the VI improvers in controlling the effect of temperature on viscosity in hydraulic fluids using a mixture of tri(wo-butyl) phosphate/Durad base stocks.
- Durad 150 (available from FMC Corporation, Princeton, New Jersey, USA) was used at 9.9% in the first two examples whereas Durad 220B (available from FMC Corporation Princeton, New Jersey, USA) was used at 7.5 % in the third example.
- the tri(w ⁇ -butyl) phosphate concentration ranged from 75.1 to 80.1 % . Base stocks only were used for this study.
- the first VI improver was referred to as "HPC 3251 " which is a more shear stable polyalkylacrylate available from Royal Lubricants Company Inc., East Hanover, New Jersey, USA; the second VI improver was PA 6538, a polyalkylmethacrylate available from Rohm & Haas, Spring House, Pennyslvania, USA; and the third VI improver was PRS available from Rohm & Haas (Spring House, Pennsylvania, USA).
- the viscosity of these formulations was tested at 100°C (212°F). At this temperature, each of these formulations required a concentration of VI improver of greater than 9 weight percent to achieve a viscosity of from 3- 4 cSt.
- VI improvers will have a deleterious effect on the viscosity of the formulation at -65 ° such that, at this temperature, the formulation would be too viscous. Accordingly, these VI improvers are unacceptable for use in the claimed invention.
- Example 3 The purpose of this example illustrates how a hydraulic fluid composition comprising a linear polyoxyalkylene material could be formulated for use in the formulations of this invention.
- Formulation 2 a formulation of this invention, could be prepared by blending the following components:
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Abstract
Description
Claims
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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US35353394A | 1994-12-09 | 1994-12-09 | |
US353533 | 1994-12-09 | ||
PCT/US1995/015984 WO1996017517A1 (en) | 1994-12-09 | 1995-12-08 | Hydraulic fluids for use in aircraft |
Publications (2)
Publication Number | Publication Date |
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EP0871690A4 EP0871690A4 (en) | 1998-10-21 |
EP0871690A1 true EP0871690A1 (en) | 1998-10-21 |
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Application Number | Title | Priority Date | Filing Date |
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EP95944797A Withdrawn EP0871690A1 (en) | 1994-12-09 | 1995-12-08 | Hydraulic fluids for use in aircraft |
Country Status (3)
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EP (1) | EP0871690A1 (en) |
AU (1) | AU5294696A (en) |
WO (1) | WO1996017517A1 (en) |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
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US5817606A (en) * | 1996-08-08 | 1998-10-06 | Rohm And Haas Company | Viscosity index improving additives for phosphate ester-containing hydraulic fluids |
WO2000024848A1 (en) * | 1998-10-23 | 2000-05-04 | Exxonmobil Research And Engineering Company | Phosphate ester base stocks and aircraft hydraulic fluids comprising the same |
JP4431281B2 (en) | 1998-10-23 | 2010-03-10 | エクソンモービル リサーチ アンド エンジニアリング カンパニー | Phosphate ester base oil and aircraft hydraulic fluid containing the base oil |
AU761121B2 (en) * | 1998-11-10 | 2003-05-29 | Exxonmobil Research And Engineering Company | Phosphate ester base stocks comprising mixed (N)-butyl/isobutyl phosphate esters and aircraft hydraulic fluids comprising the same |
US6391225B1 (en) | 2000-02-25 | 2002-05-21 | Exxonmobil Research And Engineering Company | Phosphate ester hydraulic fluids with improved properties (law935) |
US6703355B2 (en) | 2000-08-04 | 2004-03-09 | Exxonmobil Research And Engineering Company | Method for lubricating high pressure hydraulic system using phosphate ester hydraulic fluid |
US20030047709A1 (en) * | 2001-04-20 | 2003-03-13 | Marc-Andre Poirier | Monoepoxycyclohexyl carboxylates and aircraft hydraulic fluids containing same |
EP1397471A4 (en) * | 2001-04-20 | 2009-07-22 | Exxonmobil Res & Eng Co | Functional fluids with servo valve erosion resistance |
CA2504891C (en) * | 2002-11-04 | 2012-05-29 | Solutia Inc. | Functional fluid compositions containing erosion inhibitors |
US7582225B2 (en) * | 2005-06-14 | 2009-09-01 | Solutia, Inc. | High performance phosphate ester hydraulic fluid |
WO2018108869A1 (en) | 2016-12-14 | 2018-06-21 | Evonik Oil Additives Gmbh | Use of polyesters as viscosity index improvers for aircraft hydraulic fluids |
ES2941699T3 (en) | 2020-12-18 | 2023-05-24 | Evonik Operations Gmbh | Acrylate-Olefin Copolymers as High Viscosity Base Fluids |
CA3197881A1 (en) | 2022-05-24 | 2023-11-24 | Evonik Operations Gmbh | Acrylate-olefin copolymers as high viscosity base fluids |
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US3679587A (en) * | 1970-03-10 | 1972-07-25 | Monsanto Co | Functional fluid compositions containing perfluoro surfactants |
BE792993A (en) * | 1971-12-20 | 1973-06-19 | Monsanto Co | COMPOSITIONS OF FUNCTIONAL FLUIDS CONTAINING OXIDE STABILIZERS |
US3951837A (en) * | 1973-09-24 | 1976-04-20 | Mcdonnell Douglas Corporation | Functional fluid compositions |
US4206067A (en) * | 1978-10-02 | 1980-06-03 | Chevron Research Company | Thermally stabilized erosion-inhibited functional fluids containing perhalometal compounds and an organic base |
JP3420235B2 (en) * | 1992-06-11 | 2003-06-23 | ソリユテイア・インコーポレイテツド | Functional fluid |
-
1995
- 1995-12-08 EP EP95944797A patent/EP0871690A1/en not_active Withdrawn
- 1995-12-08 AU AU52946/96A patent/AU5294696A/en not_active Abandoned
- 1995-12-08 WO PCT/US1995/015984 patent/WO1996017517A1/en not_active Application Discontinuation
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No further relevant documents disclosed * |
See also references of WO9617517A1 * |
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AU5294696A (en) | 1996-06-26 |
WO1996017517A1 (en) | 1996-06-13 |
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