US20040127370A1 - Hydraulic fluids with erosion resistance - Google Patents

Hydraulic fluids with erosion resistance Download PDF

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US20040127370A1
US20040127370A1 US10/703,987 US70398703A US2004127370A1 US 20040127370 A1 US20040127370 A1 US 20040127370A1 US 70398703 A US70398703 A US 70398703A US 2004127370 A1 US2004127370 A1 US 2004127370A1
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alkali metal
weight
perfluorophosphate
carbon atoms
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Marc Poirier
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ExxonMobil Technology and Engineering Co
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Assigned to EXXONMOBIL RESEARCH AND ENGINEERING COMPANY reassignment EXXONMOBIL RESEARCH AND ENGINEERING COMPANY ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: POIRIOR, MARC ANDRE
Publication of US20040127370A1 publication Critical patent/US20040127370A1/en
Priority to US11/655,540 priority patent/US20070129264A1/en
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    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M169/00Lubricating 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
    • C10M169/04Mixtures of base-materials and additives
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/085Phosphorus oxides, acids or salts
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/08Aldehydes; Ketones
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/02Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/08Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate type
    • C10M2209/084Acrylate; Methacrylate
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/02Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
    • C10M2223/04Phosphate esters
    • C10M2223/0405Phosphate esters used as base material
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2010/00Metal present as such or in compounds
    • C10N2010/02Groups 1 or 11
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/06Oiliness; Film-strength; Anti-wear; Resistance to extreme pressure
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/08Hydraulic fluids, e.g. brake-fluids

Definitions

  • the present invention is concerned with enhancing the anti-erosion properties of phosphate ester based fluids used in transmitting power in hydraulic systems.
  • Hydraulic fluids are used in a wide variety of industrial applications, including control systems for jet turbines, steam turbines, aircraft and aerospace equipment.
  • control systems for jet turbines, steam turbines, aircraft and aerospace equipment For example, in aircraft equipment they are used as the power transmitting medium in operating various moving parts of the aircraft, such as wing flaps, ailerons, rudders and landing gear.
  • Organic phosphate ester fluids have been recognized as a preferred base stock for use in hydraulic fluids. Indeed, in present commercial aircraft hydraulic fluids, phosphate esters are among the most commonly used base stocks.
  • composition comprising:
  • compositions of the present invention comprise a major amount of a phosphate ester base stock.
  • the phosphate esters typically employed in such base stocks include trialkyl phosphates, dialkylaryl phosphates, and triaryl phosphates having alkyl groups of from 3 to 8 and preferably 4 to 5 carbon atoms.
  • Such phosphate ester base stocks are the preferred base stocks of the instant invention.
  • Particularly preferred phosphate esters are trialkyl phosphate esters and among these tri-n-butyl phosphate and tri-isobutyl phosphate are preferred.
  • the amount of each type of phosphate ester comprising the base stock can vary depending upon the type of phosphate esters involved.
  • the phosphate ester base stock used in the present invention comprises, based on the total weight of the base stock, (a) from about 10 wt % to about 100 wt %, and preferably from about 20 wt % to about 90 wt % of a trialkyl phosphate; (b) from 0 wt % to about 75 wt % and preferably from 0 wt % to about 50 wt % of a dialkylaryl phosphate; (c) from 0 wt % to about 30 wt %, and preferably from 0 wt % to 10 wt % of an alkyl diaryl phosphate; and (d) from 0 wt % to about 20 wt % and preferably from 0 wt % to about 15 wt % of a triaryl phosphate
  • composition of the present invention includes a minor but effective amount of both an alkali metal perfluoro phosphate and a mono epoxy cyclohexane carboxylate.
  • the composition will include from about 0.01 wt % to about 0.5 wt % based on the weight of the composition, of an alkali metal perfluoro phosphate or mixtures of alkali metal perfluorophosphate.
  • Alkali metals include lithium, sodium, potassium, rubidium and cesium.
  • the alkali metal perfluorophosphate is potassium perfluoro phosphate.
  • composition of the present invention also will include a mono epoxyclyclohexane carboxylate. Specifically the composition will include from about 1 wt % to about 10 wt % of a mono epoxide represented by the formula
  • R is selected from the group consisting of alkyl groups having from 1 to 10 carbon atoms, and —(CH 2 ) n —OR 1 where R 1 is an alkyl group of 1 to 10 carbon atoms and n is an integer of from 1 to 3.
  • R is a branched alkyl group of 4 to 8 carbon atoms and more preferably R is a 2-ethyl-1-hexyl group.
  • the hydraulic fluid compositions of this invention further comprise an antioxidant or mixture of antioxidants in an amount effective to inhibit oxidation of the fluid or its components.
  • Suitable antioxidants include polyphenols, trialkyl phenols and di(alkyl phenyl) amines.
  • Representative examples include: bis (3,5-di-tert-butyl-4-hydroxy phenyl) methane (e.g., Hitec® 4702 from Ethyl Corp.); 1,3,5-trimethyl-2,4,6-tris (3,5-di-tert-butyl-4-hydroxy phenyl) benzene (e.g., Ethanox® 330 from Albemarle Corp.); tetrakis (methylene (3,5-di-tert-butyl-4-hydroxy hydrocinnamate) methane (e.g., Irganox® 1010 from Ciba Geigy); di(n-octylphenyl) amine (e.g., Vanlube 81 from Vanderbilt); and the like.
  • bis (3,5-di-tert-butyl-4-hydroxy phenyl) methane e.g., Hitec® 4702 from Ethyl Corp.
  • the antioxidants or mixture of antioxidants typically will be used in amounts ranging from about 0.5 wt % to about 3 wt % based on the total weight of the composition.
  • compositions of this invention further comprise an effective amount of a rust inhibitor or a mixture of rust inhibitors.
  • rust inhibitors include calcium dinonylnaphthalene, a Group I or Group II metal over based sulfurized phenate and the like.
  • the rust inhibitor or mixture thereof is employed at from about 0.001 wt % to about 1 wt % based on the weight of the composition.
  • compositions further comprise a viscosity index improver (VII).
  • VII viscosity index improver
  • Especially preferred VII's are alkyl poly acrylates and alkyl polymethacrylate ester polymers in which at least 85% by weight have a molecular weight in the range of about 50,000 to about 100,000, and where the alkyl groups are preferably n-hexyl and isodecyl.
  • composition of the invention can optionally contain further additives such as copper corrosion inhibitors, anti foaming agents, dyes and the like.
  • a fluid composition was prepared by blending 66.8 wt % of tri-n-butyl phosphate, 12.1 wt % alkylated triphenyl phosphate; 6.2 wt % of a VI improver; 5.7 wt % of a mono epoxycyclohexane carboxylate; 0.05 wt % KPF 6 ; and the balance antioxidants, rust inhibitors dye and defoamer.
  • the fluid was then tested in an electro-deposition test developed by Boeing Aircraft Company that simulates the tendency of deposit formation in aircraft components. The results are given in Table 1.
  • Example 1 For comparative purposes a composition was prepared as in Example 1 but which contained as anti-erosion agent 0.05 wt % of a mixture of potassium perfluoro-octyl sulfonates (i.e., FC-98® from 3M) in lieu of KPF 6 . This fluid was also subjected to the electro-deposits test and the results are given in Table 1. TABLE 1 Properties Example 1 Comp.
  • Example 1 and Comparative Example 1 were subjected to an erosion rig test according to AS 1241. The tests were run at 225° F. and 275° F. and the pressure maintained at 3000 psi. The leakage rate was measured throughout the run. The results are shown in Table 2. TABLE 2 Initial Final Leakage, Leakage Valve Test Flow, Flow, Delta Run Fluid Positions Temp. cc/min cc/min cc/min Hours Com- 6&8 275° F. 400 355 65 524 parative 1 Example 1 5&7 225° F. 288 200 88 739
  • a fluid composition was prepared containing: 78.7 wt % tributyl phosphate; 11.8 wt % isopropylated triphenyl phosphate; 6.2 wt % of a poly alkylacrylate VII; 2.3 wt % of a cyclo aliphatic diepoxide; 0.01 wt % of NH 4 PF 6 and the balance antioxidants, rust inhibitors, dye and defoamers.
  • the composition was then subjected to the anti erosion rig test of Example 2 with the results set forth in Table 3. Included in Table 3 are the results of Example 2 using the fluid of Example 1. TABLE 3 Initial Final Test Leakage Leakage Delta Run Fluid Temp. Flow, cc/min Flow, cc/min cc/min Hours Comparative 3 225° F. 222 429 207 244 Example 1 225° F. 288 200 88 739

Abstract

The erosion resistance of phosphate ester based hydraulic fluids has been found to be enhanced by incorporating in the fluid a minor amount of an alkali metal perfluorophosphate and a mono epoxycyclohexane carboxylate.

Description

  • This application claims the benefit of U.S. Serial No. 60/426,946 filed Nov. 15, 2002.[0001]
  • FIELD OF INVENTION
  • The present invention is concerned with enhancing the anti-erosion properties of phosphate ester based fluids used in transmitting power in hydraulic systems. [0002]
  • BACKGROUND OF INVENTION
  • Hydraulic fluids are used in a wide variety of industrial applications, including control systems for jet turbines, steam turbines, aircraft and aerospace equipment. For example, in aircraft equipment they are used as the power transmitting medium in operating various moving parts of the aircraft, such as wing flaps, ailerons, rudders and landing gear. [0003]
  • The proper functioning of such important control mechanisms dictate that the hydraulic fluids meet stringent performance requirements including thermal stability, fire resistance, hydrolytic stability and elastomer compatibility, to mention a few. [0004]
  • Organic phosphate ester fluids have been recognized as a preferred base stock for use in hydraulic fluids. Indeed, in present commercial aircraft hydraulic fluids, phosphate esters are among the most commonly used base stocks. [0005]
  • In order to meet the many performance criteria established for hydraulic fluids, and especially aircraft hydraulic fluids, it is common practice to incorporate various additives in base stocks. For example, experience has shown that orifices in the servo control valves of aircraft hydraulic systems are subject to erosion which is attributed to streaming current induced by fluid flow. Valve orifice erosion, if extensive, can greatly impair the functioning of the valve as a precise control mechanism. Therefore, various additives have been used in hydraulic fluids as erosion inhibitors. [0006]
  • Nonetheless there remains a need for increased choice of useful erosion inhibitors, especially for improved erosion inhibitors for phosphate ester based hydraulic fluids. [0007]
  • SUMMARY OF INVENTION
  • It has now been discovered that by incorporating a minor amount of both an alkali metal perfluorophosphate and a mono epoxycyclohexane carboxylate into a major amount of a phosphate ester based hydraulic fluid the anti erosion properties of the composition are surprisingly enhanced. Thus, in one embodiment there is provided a composition comprising: [0008]
  • a major amount of a phosphate ester base stock; and [0009]
  • a minor amount of an alkali metal perfluoro phosphate and a mono epoxycyclohexane carboxylate.[0010]
  • DETAILED DESCRIPTION OF INVENTION
  • The compositions of the present invention comprise a major amount of a phosphate ester base stock. The phosphate esters typically employed in such base stocks include trialkyl phosphates, dialkylaryl phosphates, and triaryl phosphates having alkyl groups of from 3 to 8 and preferably 4 to 5 carbon atoms. Such phosphate ester base stocks are the preferred base stocks of the instant invention. Particularly preferred phosphate esters are trialkyl phosphate esters and among these tri-n-butyl phosphate and tri-isobutyl phosphate are preferred. [0011]
  • The amount of each type of phosphate ester comprising the base stock can vary depending upon the type of phosphate esters involved. The phosphate ester base stock used in the present invention comprises, based on the total weight of the base stock, (a) from about 10 wt % to about 100 wt %, and preferably from about 20 wt % to about 90 wt % of a trialkyl phosphate; (b) from 0 wt % to about 75 wt % and preferably from 0 wt % to about 50 wt % of a dialkylaryl phosphate; (c) from 0 wt % to about 30 wt %, and preferably from 0 wt % to 10 wt % of an alkyl diaryl phosphate; and (d) from 0 wt % to about 20 wt % and preferably from 0 wt % to about 15 wt % of a triaryl phosphate. [0012]
  • The composition of the present invention includes a minor but effective amount of both an alkali metal perfluoro phosphate and a mono epoxy cyclohexane carboxylate. [0013]
  • Specifically the composition will include from about 0.01 wt % to about 0.5 wt % based on the weight of the composition, of an alkali metal perfluoro phosphate or mixtures of alkali metal perfluorophosphate. Alkali metals, of course, include lithium, sodium, potassium, rubidium and cesium. Preferably the alkali metal perfluorophosphate is potassium perfluoro phosphate. [0014]
  • The composition of the present invention also will include a mono epoxyclyclohexane carboxylate. Specifically the composition will include from about 1 wt % to about 10 wt % of a mono epoxide represented by the formula [0015]
    Figure US20040127370A1-20040701-C00001
  • where R is selected from the group consisting of alkyl groups having from 1 to 10 carbon atoms, and —(CH[0016] 2)n—OR1 where R1 is an alkyl group of 1 to 10 carbon atoms and n is an integer of from 1 to 3. Preferably R is a branched alkyl group of 4 to 8 carbon atoms and more preferably R is a 2-ethyl-1-hexyl group.
  • In a preferred embodiment the hydraulic fluid compositions of this invention further comprise an antioxidant or mixture of antioxidants in an amount effective to inhibit oxidation of the fluid or its components. Suitable antioxidants include polyphenols, trialkyl phenols and di(alkyl phenyl) amines. Representative examples include: bis (3,5-di-tert-butyl-4-hydroxy phenyl) methane (e.g., Hitec® 4702 from Ethyl Corp.); 1,3,5-trimethyl-2,4,6-tris (3,5-di-tert-butyl-4-hydroxy phenyl) benzene (e.g., Ethanox® 330 from Albemarle Corp.); tetrakis (methylene (3,5-di-tert-butyl-4-hydroxy hydrocinnamate) methane (e.g., Irganox® 1010 from Ciba Geigy); di(n-octylphenyl) amine (e.g., Vanlube 81 from Vanderbilt); and the like. [0017]
  • The antioxidants or mixture of antioxidants typically will be used in amounts ranging from about 0.5 wt % to about 3 wt % based on the total weight of the composition. [0018]
  • In another preferred embodiment the compositions of this invention further comprise an effective amount of a rust inhibitor or a mixture of rust inhibitors. Representative examples of rust inhibitors include calcium dinonylnaphthalene, a Group I or Group II metal over based sulfurized phenate and the like. Typically the rust inhibitor or mixture thereof is employed at from about 0.001 wt % to about 1 wt % based on the weight of the composition. [0019]
  • In yet another embodiment the compositions further comprise a viscosity index improver (VII). Especially preferred VII's are alkyl poly acrylates and alkyl polymethacrylate ester polymers in which at least 85% by weight have a molecular weight in the range of about 50,000 to about 100,000, and where the alkyl groups are preferably n-hexyl and isodecyl. [0020]
  • The composition of the invention can optionally contain further additives such as copper corrosion inhibitors, anti foaming agents, dyes and the like. [0021]
  • EXAMPLES Example 1 and Comparative Example 1
  • A fluid composition was prepared by blending 66.8 wt % of tri-n-butyl phosphate, 12.1 wt % alkylated triphenyl phosphate; 6.2 wt % of a VI improver; 5.7 wt % of a mono epoxycyclohexane carboxylate; 0.05 wt % KPF[0022] 6; and the balance antioxidants, rust inhibitors dye and defoamer. The fluid was then tested in an electro-deposition test developed by Boeing Aircraft Company that simulates the tendency of deposit formation in aircraft components. The results are given in Table 1.
  • For comparative purposes a composition was prepared as in Example 1 but which contained as anti-erosion agent 0.05 wt % of a mixture of potassium perfluoro-octyl sulfonates (i.e., FC-98® from 3M) in lieu of KPF[0023] 6. This fluid was also subjected to the electro-deposits test and the results are given in Table 1.
    TABLE 1
    Properties Example 1 Comp. Example 1
    Electrode appearance Clean Clean
    Electrode 2A 2C 2A 2C
    Metal wt loss, mg  0.70 18.80   1.50 5.20
    Deposit wt, 1st rinse, mg 10.90 2.80 13.10 3.0 
    Deposits wt, 1st soak, mg 10.70 3.00 10.80 2.5 
    Deposit wt, 2nd soak, mg  9.90 2.40 10.40 2.50
    Fluid appearance after test Purple Purple Brownish Brownish
  • Example 2, Comparative Example 2
  • The anti-erosion performance of Example 1 and Comparative Example 1 were subjected to an erosion rig test according to AS 1241. The tests were run at 225° F. and 275° F. and the pressure maintained at 3000 psi. The leakage rate was measured throughout the run. The results are shown in Table 2. [0024]
    TABLE 2
    Initial Final
    Leakage, Leakage
    Valve Test Flow, Flow, Delta Run
    Fluid Positions Temp. cc/min cc/min cc/min Hours
    Com- 6&8 275° F. 400 355 65 524
    parative 1
    Example 1 5&7 225° F. 288 200 88 739
  • Comparative Example 3
  • A fluid composition was prepared containing: 78.7 wt % tributyl phosphate; 11.8 wt % isopropylated triphenyl phosphate; 6.2 wt % of a poly alkylacrylate VII; 2.3 wt % of a cyclo aliphatic diepoxide; 0.01 wt % of NH[0025] 4 PF6 and the balance antioxidants, rust inhibitors, dye and defoamers. The composition was then subjected to the anti erosion rig test of Example 2 with the results set forth in Table 3. Included in Table 3 are the results of Example 2 using the fluid of Example 1.
    TABLE 3
    Initial Final
    Test Leakage Leakage Delta Run
    Fluid Temp. Flow, cc/min Flow, cc/min cc/min Hours
    Comparative 3 225° F. 222 429 207 244
    Example 1 225° F. 288 200  88 739
  • The data shows that the combination of KPF[0026] 6 and a mono epoxy cyclohexane carboxylate provide surprisingly lower erosion as determined by the leakage flow.

Claims (7)

What is claimed is:
1. A fluid composition comprising:
a major amount of a phosphate ester base stock and a minor amount of an alkali metal perfluorophosphate or mixture of alkali metal perfluorophosphates and a mono epoxycyclohexane carboxylate.
2. The composition of claim 1 wherein the alkali metal perfluorophosphate or mixtures of alkali metal perfluorophosphates are present in an amount of from about 0.01 wt % to about 0.5 wt % based on the weight of the composition.
3. The composition of claim 2 wherein the mono epoxycyclohexane carboxylate is represented by the formula
Figure US20040127370A1-20040701-C00002
where R is an alkyl group of 1 to 10 carbon atoms or —(CH2)n—OR, where n is an integer of 1 to 3 and R1 is an alkyl group of 1 to 10 and wherein said mono epoxycyclohexane carboxylate is present from about 1 wt % to about 10 wt % based on the weight of the composition.
4. A hydraulic fluid composition comprising:
(a) a major amount of a phosphate ester base stock comprising, based on the weight of base stock;
(i) from 10 to 100 wt % of trialkyl phosphate;
(ii) from 0 to 75 wt % of dialkyl aryl phosphates;
(iii) from 0 to 30 wt % of alkyldiaryl phosphates; and
(iv) from 0 to 20 wt % of alkylated triaryl phosphates, and wherein the alkyl groups of (i) to (iv) have from 3 to 8 carbon atoms; and
(b) both
(i) from about 0.01 wt % to about 0.5 wt %, based on the weight of the composition of an alkali metal perfluorophosphate or mixtures of alkali-metal perfluorophosphate; and
(ii) from about 1 wt % to about 10 wt %, based on the weight of the composition, of a compound having the formula
Figure US20040127370A1-20040701-C00003
where R is an alkyl group of 1 to 10 carbon atoms or —(CH2)nOR, where n is an integer of 1 to 3 and R is an alkyl group of 1 to 10 carbon atoms.
5. The composition of claim 4 wherein the alkali metal of the perfluorophosphate is potassium and R is a branched alkyl group of 4 to 8 carbon atoms.
6. The composition of claim 5 including a poly(alkylacrylate) or poly(alkylmethacrylate) viscosity index improver (VII).
7. The composition of claim 6 wherein the VII is present at from about 3 wt % to about 10 wt % based on the weight of the composition.
US10/703,987 2002-11-15 2003-11-07 Hydraulic fluids with erosion resistance Abandoned US20040127370A1 (en)

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CN102977972A (en) * 2011-09-02 2013-03-20 中国石油化工股份有限公司 Method for improving steam turbine oil operation performances

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US2636861A (en) * 1950-06-09 1953-04-28 Shell Dev Hydraulic fluid
US2732398A (en) * 1953-01-29 1956-01-24 cafiicfzsojk
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US3707501A (en) * 1970-06-29 1972-12-26 Stauffer Chemical Co Hydraulic fluids containing certain quaternary phosphonium salts of phosphorus acids
US3723320A (en) * 1971-12-20 1973-03-27 Monsanto Co Functional fluid compositions containing epoxide stabilizers
US4252662A (en) * 1974-02-11 1981-02-24 Stauffer Chemical Company Functional fluids containing ammonium salts of phosphorus acids
US4324674A (en) * 1980-08-28 1982-04-13 Chevron Research Company Amine salt stabilized phosphate ester-based functional fluid
US5550277A (en) * 1995-01-19 1996-08-27 Paciorek; Kazimiera J. L. Perfluoroalkyl and perfluoroalkylether substituted aromatic phosphates, phosphonates and related compositions
US5817606A (en) * 1996-08-08 1998-10-06 Rohm And Haas Company Viscosity index improving additives for phosphate ester-containing hydraulic fluids
US6184187B1 (en) * 1998-04-07 2001-02-06 E. I. Dupont De Nemours And Company Phosphorus compounds and their use as corrosion inhibitors for perfluoropolyethers

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Publication number Priority date Publication date Assignee Title
US2636861A (en) * 1950-06-09 1953-04-28 Shell Dev Hydraulic fluid
US2732398A (en) * 1953-01-29 1956-01-24 cafiicfzsojk
US3679587A (en) * 1970-03-10 1972-07-25 Monsanto Co Functional fluid compositions containing perfluoro surfactants
US3707501A (en) * 1970-06-29 1972-12-26 Stauffer Chemical Co Hydraulic fluids containing certain quaternary phosphonium salts of phosphorus acids
US3723320A (en) * 1971-12-20 1973-03-27 Monsanto Co Functional fluid compositions containing epoxide stabilizers
US4252662A (en) * 1974-02-11 1981-02-24 Stauffer Chemical Company Functional fluids containing ammonium salts of phosphorus acids
US4324674A (en) * 1980-08-28 1982-04-13 Chevron Research Company Amine salt stabilized phosphate ester-based functional fluid
US5550277A (en) * 1995-01-19 1996-08-27 Paciorek; Kazimiera J. L. Perfluoroalkyl and perfluoroalkylether substituted aromatic phosphates, phosphonates and related compositions
US5817606A (en) * 1996-08-08 1998-10-06 Rohm And Haas Company Viscosity index improving additives for phosphate ester-containing hydraulic fluids
US6184187B1 (en) * 1998-04-07 2001-02-06 E. I. Dupont De Nemours And Company Phosphorus compounds and their use as corrosion inhibitors for perfluoropolyethers

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102977972A (en) * 2011-09-02 2013-03-20 中国石油化工股份有限公司 Method for improving steam turbine oil operation performances
CN102977972B (en) * 2011-09-02 2015-08-19 中国石油化工股份有限公司 Improve the method for turbine oil operating performance

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