[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

US3707500A - Functional fluid composition - Google Patents

Functional fluid composition Download PDF

Info

Publication number
US3707500A
US3707500A US77675A US3707500DA US3707500A US 3707500 A US3707500 A US 3707500A US 77675 A US77675 A US 77675A US 3707500D A US3707500D A US 3707500DA US 3707500 A US3707500 A US 3707500A
Authority
US
United States
Prior art keywords
phosphate
weight
trialkyl
functional fluid
mixture
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.)
Expired - Lifetime
Application number
US77675A
Inventor
Joseph J Romano
John J Shatynski
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Akzo America Inc
Original Assignee
Stauffer Chemical Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Stauffer Chemical Co filed Critical Stauffer Chemical Co
Application granted granted Critical
Publication of US3707500A publication Critical patent/US3707500A/en
Assigned to AKZO AMERICA INC., A CORP. OF DE reassignment AKZO AMERICA INC., A CORP. OF DE ASSIGNMENT OF ASSIGNORS INTEREST. Assignors: STAUFFER CHEMICAL COMPANY
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • 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
    • C10M3/00Liquid compositions essentially based on lubricating components other than mineral lubricating oils or fatty oils and their use as lubricants; Use as lubricants of single liquid substances
    • 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
    • C10M2201/02Water
    • 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
    • C10M2207/02Hydroxy compounds
    • C10M2207/023Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/025Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings with condensed rings
    • 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
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/121Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
    • C10M2207/123Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms polycarboxylic
    • 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
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/129Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more carbon atoms
    • 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
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/22Acids obtained from polymerised unsaturated acids
    • 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
    • C10M2207/28Esters
    • C10M2207/282Esters of (cyclo)aliphatic oolycarboxylic acids
    • 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
    • C10M2207/28Esters
    • C10M2207/34Esters having a hydrocarbon substituent of thirty or more carbon atoms, e.g. substituted succinic acid derivatives
    • 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
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/22Heterocyclic nitrogen compounds
    • 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
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/22Heterocyclic nitrogen compounds
    • C10M2215/221Six-membered rings containing nitrogen and carbon only
    • 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
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/22Heterocyclic nitrogen compounds
    • C10M2215/225Heterocyclic nitrogen compounds the rings containing both nitrogen and oxygen
    • 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
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/22Heterocyclic nitrogen compounds
    • C10M2215/225Heterocyclic nitrogen compounds the rings containing both nitrogen and oxygen
    • C10M2215/226Morpholines
    • 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
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/30Heterocyclic compounds
    • 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
    • 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
    • C10M2223/041Triaryl phosphates
    • 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
    • C10M2223/042Metal salts thereof
    • 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
    • C10M2229/00Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
    • C10M2229/02Unspecified siloxanes; Silicones
    • 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
    • C10M2229/00Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
    • C10M2229/04Siloxanes with specific structure
    • C10M2229/05Siloxanes with specific structure containing atoms other than silicon, hydrogen, oxygen or carbon
    • 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

  • a functional fluid composition comprising a homogeneous mixture of materials consisting essentiallly of trialkyl phosphate, tricresyl phosphate, trixylenyl phosphate, a viscosity index improver, rust inhibitor, metal deactivator, a dye and an antifoam agent.
  • compositions suitable for special purposes require a combination of properties which ordinary compositions fail to meet in many respects.
  • the properties which are required for safe and satisfactory low temperature operation include low pour points so that the composition will operate at a temperature at least as low as 40 F., to -60 F.
  • Another important property which is desirable for such uses is a flat viscosity temperature curve, that is, a high viscosity index, so that the material is operable over a wide range of temperatures, such as are encountered in the operation of aircraft.
  • One of the key properties which must *be considered for both commercial aircraft and military use is minimum flammability.
  • Other inherent qualities include a relatively high boiling point, low corrosion characteristics and low oxidation susceptibility.
  • trialkyl phosphates have been to add thereto a small amount of triaryl phosphate such as diphenyl cresyl phosphate a certain proportion of a linear polymer of methacrylic acid esters and a small amount of an epoxide composition such as glycidyl hydrocarbyl ethers and hydrocarbon epoxides, see Pat. No. 2,636,861.
  • triaryl phosphate such as diphenyl cresyl phosphate a certain proportion of a linear polymer of methacrylic acid esters
  • an epoxide composition such as glycidyl hydrocarbyl ethers and hydrocarbon epoxides
  • trialkyl phosphates can be successfully employed as functional fluids when combined with certain other materials within certain limitations to provide the properties for the functional fluid.
  • the trialkyl phosphate can be combined with tricresyl phosphate, trixylenyl phosphate, a viscosity index 3,707,500 Patented Dec. 26, 1972 DETAILED DESCRIPTION OF THE INVENTION
  • the trialkyl phosphates useful with the present invention are present in amounts from about 50 to about by weight and preferably from about 65 to about 75% by weight.
  • the trialkyl phosphates which give optimum results are those wherein each of the alkyl groups contain from 3 to 12 carbon atoms, preferably from 4 to 9 carbon atoms.
  • the alkyl groups must be of a straight chained configuration.
  • a single trialkyl phosphate may contain the same alkyl group in all three positions or may possess a mixture of different alkyl groups. Mixtures of various trialkyl phosphate may be used.
  • Suitable species of trialkyl phosphates which are employed in the composition of the present invention include tripropyl phosphates, tributyl phosphates, trihexyl phosphates, trioctyl phosphates, dipropyl octylphosphate, dibutyl octyl phosphate, dipropyl hexyl phosphate, dihexyl octyl phosphate, dihexyl propyl phosphate, propyl butyl octyl phosphate.
  • the trialkyl phosphates of the present invention must be combined with at least one base stock material comprising tricresyl phosphate or trixylenyl phosphate but preferably consisting of a combined mixture of tricresyl phosphate and trixylenyl phosphate which function also as a thickener.
  • the amount of tricresyl phosphate is in the range between about 0 to about 25% while the trixylenyl phosphate is in the range between about 0 and about 25 by weight, preferably about 5 to about 15% tricresyl phosphate and about 5 to about 15% tricresyl phosphate.
  • a conventional polymeric material is then blended with the mixture of trialkyl phosphate and base stock material which polymeric material functions as a viscosity index improver.
  • the polymeric material useable with the present invention is a mixture of from about 10 to about 55% by weight polymethacrylates, polyacrylates each containing from 1 to 20 carbon atoms.
  • the polymeric materials may be within a solvent carrier such as di-2- ethyl hexyl sebacate, dioctyl adipate, di-2-ethyl hexyl adipate or other conventional carriers.
  • the polymeric material may be any combination of these materials. This material is thoroughly blended with the combination of ingredients to form a uniform material. The amount of material is in the range between about 5 and about 20% by weight.
  • a rust inhibitor within a solvent carrier such as an alkyl succinic acid and their derivatives is blended with the materials.
  • This latter material is essential to the present invention and is present in amounts between about 0.01 and about 0.5% by Weight.
  • a corrosion inhibitor such as benzotriazole, quinizarin or the like in an amount ranging between about 0.001 and about 0.5% by Weight is added to the mixture and thoroughly blended therewith.
  • a dye which may range between 5 and 20 parts per million is added thereto and blended therewith as is conventional in the art.
  • a conventional silicon antifoaming agent is added thereto which may range between 5 and 50 parts per million.
  • the functional fluids may be prepared in a manner illustrated in the following examples:
  • Example 1 A base stock material consisting of tricresyl phosphate in an amount of 10.45 weight percent was thoroughly blended with 8.55 weight percent of trixylenyl phosphate to attain a viscosity of 155 Saybolt Universal Seconds measured at 100 F. This blend of materials was blended with 68.96 weight percent of tributyl phosphate until the materials were throughly intermixed. Thereafter, 12 weight percent of a mixture of about 40% of a polyalkyl methacrylate and about 60% di-Z-ethyl hexyl sebacate solvent carrier were thoroughly blended therewith. Then, a conventional alkyl succinic acid rust inhibitor in an amount of 0.02 weight percent within a solvent carrier was blended therewith.
  • Example 2 The thermal stability of a conventional functional fluid was tested and compared to the fluid of the present invention.
  • a sample of a commercially available material was obtained and tested in accordance with the procedures outlined in Table V.
  • the active material was octyl diphenylphosphate.
  • the viscosity change measured in centistrokes at 100 F. was 0.25 while the neutralization number change measured in milligrams potassium hydroxide per gram was +7.57.
  • a comparison to the thermal stability as indicated in Table 5 of Example 1 illustrates the superiority of the fluid of the present invention.
  • a composition useful as a base stock in hydraulic fluids which consists essentially of at least 50 to about by weight of a tiralkyl phosphate selected from the group consisting of tripropyl phosphate, tributyl phosphate, trihexyl phosphate, trioctyl phosphate, dipropyl octyl phosphate, dibutyl octyl phosphate, dipropyl hexyl phosphate, dihexyl octyl phosphate, dihexyl propyl phosphate, propyl butyl octyl phosphate and mixtures thereof, and a mixture of from about 5 to about 25% by weight of tricresyl phosphate and from about 5 to about 25% by weight of trixylenyl phosphate, said mixture of tricresyl and trixylenyl phosphates having a viscosity of between about 145 to about 230 Saybolt Universal Seconds measured at
  • a hydraulic fluid consisting essentially of the base stock in accordance with claim 1 and additionally containing from about 5 to about by weight of a polymethacrylate viscosity index improver, from about 0.01 to about 0.5% by weight of an alkyl succinic acid and from about 0.001 to about 0.5 of a corrosion inhibitor selected from the group consisting of benzotriazole and quinizarin.
  • the hydraulic fluid of claim 3 additionally containing between about 5 to about 20 parts per million of a dye and between about 5 to about parts per million of an antifoaming agent.
  • the hydraulic fluid of claim 3 additionally containing up to about 5% by weight water.
  • a composition useful as a hydraulic fluid consisting essentially of from about to about by weight of tributyl phosphate, a mixture of from about 5 to about 6 15 tricresyl phosphate and from about 5 to about 15 trixylenyl phosphate, said mixture of tricresyl and trixylenyl phosphates having a viscosity between about 145 to about 230 Saybolt Universal Seconds measured to F., from about 5 to about 20% by weight of a polymethacrylate viscosity index improver containing an alkyl moiety having up to 20 carbon atoms, from about 0.001 to about 0.5 by weight of benzot'riazole, from between about 5 to about 20 parts per million of a dye, and between about 5 to about 50 parts per million of an antifoaming agent.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Lubricants (AREA)

Abstract

A FUNCTIONAL FLUID COMPOSITION COMPRISING A HOMOGENEOUS MIXTURE OF MATERIALS CONSISTING ESSENTIALLY OF TRIALKYL PHOSPHATE, TRICRESYL PHOSPHATE, TRIXYLENYL PHOSPHATE, A VISCOSITY INDEX IMPROVER, RUST INHIBITOR, METAL DEACTIVATOR, A DYE AND AN ANTIFOAM AGENT.

Description

United States Patent O 3,707,500 FUNCTIONAL FLUID COMPOSITION Joseph J. Romano, New City, N.Y., and John J. Shatynski, Hillside, N.J., assiguors to Stautfer Chemical Company, New York, N.Y.
No Drawing. Continuation of abandoned application Ser. No. 665,736, Sept. 6, 1967. This application Oct. 5, 1970, Ser. No. 77,675
Int. Cl. C09k 3/00 US. Cl. 252-78 6 Claims ABSTRACT OF THE DISCLOSURE A functional fluid composition comprising a homogeneous mixture of materials consisting essentiallly of trialkyl phosphate, tricresyl phosphate, trixylenyl phosphate, a viscosity index improver, rust inhibitor, metal deactivator, a dye and an antifoam agent.
This application is a continuation of application Ser. No. 665,736, filed Sept. 6, 1967, and now abandoned.
BACKGROUND OF THE INVENTION Compositions suitable for special purposes, such as low temperature lubrication and the operation of hydraulic mechanisms, require a combination of properties which ordinary compositions fail to meet in many respects. The properties which are required for safe and satisfactory low temperature operation include low pour points so that the composition will operate at a temperature at least as low as 40 F., to -60 F. Another important property which is desirable for such uses is a flat viscosity temperature curve, that is, a high viscosity index, so that the material is operable over a wide range of temperatures, such as are encountered in the operation of aircraft. One of the key properties which must *be considered for both commercial aircraft and military use is minimum flammability. Other inherent qualities include a relatively high boiling point, low corrosion characteristics and low oxidation susceptibility.
Numerous compositions have been suggested for the above purposes. Thus, the lower trialkyl phosphates have been suggested. However, these compositions exhibit high wear characteristics, are somewhat flammable, due in part to their volatility, and at low temperatures exhibit incompatibility with ordinary thickeners. In order to overcome these undesirable characteristics, it has been proposed to modify the trialkyl phosphates by adding thereto a small amount of ketone. However, the addition of the ketones do not impart to the fluid the properties as required for the functional fluids. An example of such a composition is described in US. Pat. 2,470,792.
Another attempt to employ the trialkyl phosphates has been to add thereto a small amount of triaryl phosphate such as diphenyl cresyl phosphate a certain proportion of a linear polymer of methacrylic acid esters and a small amount of an epoxide composition such as glycidyl hydrocarbyl ethers and hydrocarbon epoxides, see Pat. No. 2,636,861. However, these materials have not been notably successful in the performance as functional fluids in aircraft because these materials lack all the combined aforementioned properties.
BRIEF DESCRIPTION OF THE INVENTION It has been discovered that the trialkyl phosphates can be successfully employed as functional fluids when combined with certain other materials Within certain limitations to provide the properties for the functional fluid. Thus, the trialkyl phosphate can be combined with tricresyl phosphate, trixylenyl phosphate, a viscosity index 3,707,500 Patented Dec. 26, 1972 DETAILED DESCRIPTION OF THE INVENTION The trialkyl phosphates useful with the present invention are present in amounts from about 50 to about by weight and preferably from about 65 to about 75% by weight. The trialkyl phosphates which give optimum results are those wherein each of the alkyl groups contain from 3 to 12 carbon atoms, preferably from 4 to 9 carbon atoms. The alkyl groups must be of a straight chained configuration. A single trialkyl phosphate may contain the same alkyl group in all three positions or may possess a mixture of different alkyl groups. Mixtures of various trialkyl phosphate may be used. Suitable species of trialkyl phosphates which are employed in the composition of the present invention include tripropyl phosphates, tributyl phosphates, trihexyl phosphates, trioctyl phosphates, dipropyl octylphosphate, dibutyl octyl phosphate, dipropyl hexyl phosphate, dihexyl octyl phosphate, dihexyl propyl phosphate, propyl butyl octyl phosphate.
The trialkyl phosphates of the present invention must be combined with at least one base stock material comprising tricresyl phosphate or trixylenyl phosphate but preferably consisting of a combined mixture of tricresyl phosphate and trixylenyl phosphate which function also as a thickener. Thus, the amount of tricresyl phosphate is in the range between about 0 to about 25% while the trixylenyl phosphate is in the range between about 0 and about 25 by weight, preferably about 5 to about 15% tricresyl phosphate and about 5 to about 15% tricresyl phosphate. The combined mixture of tricresyl phosphate and trixylenyl phosphate are blended together to provide a viscosity of between about 145 to 230 Saybolt Universal Seconds measured at F. This blend of materials can then be combined with the trialkyl phosphate in any known manner.
A conventional polymeric material is then blended with the mixture of trialkyl phosphate and base stock material which polymeric material functions as a viscosity index improver. The polymeric material useable with the present invention is a mixture of from about 10 to about 55% by weight polymethacrylates, polyacrylates each containing from 1 to 20 carbon atoms. The polymeric materials may be within a solvent carrier such as di-2- ethyl hexyl sebacate, dioctyl adipate, di-2-ethyl hexyl adipate or other conventional carriers. The polymeric material may be any combination of these materials. This material is thoroughly blended with the combination of ingredients to form a uniform material. The amount of material is in the range between about 5 and about 20% by weight.
Thereafter, a rust inhibitor within a solvent carrier such as an alkyl succinic acid and their derivatives is blended with the materials. This latter material is essential to the present invention and is present in amounts between about 0.01 and about 0.5% by Weight. Thereafter, a corrosion inhibitor such as benzotriazole, quinizarin or the like in an amount ranging between about 0.001 and about 0.5% by Weight is added to the mixture and thoroughly blended therewith. Then, a dye which may range between 5 and 20 parts per million is added thereto and blended therewith as is conventional in the art. Also a conventional silicon antifoaming agent is added thereto which may range between 5 and 50 parts per million.
The above mixture of components has the requisite properties to be useable as a functional fluid.
The functional fluids may be prepared in a manner illustrated in the following examples:
Example 1 A base stock material consisting of tricresyl phosphate in an amount of 10.45 weight percent was thoroughly blended with 8.55 weight percent of trixylenyl phosphate to attain a viscosity of 155 Saybolt Universal Seconds measured at 100 F. This blend of materials was blended with 68.96 weight percent of tributyl phosphate until the materials were throughly intermixed. Thereafter, 12 weight percent of a mixture of about 40% of a polyalkyl methacrylate and about 60% di-Z-ethyl hexyl sebacate solvent carrier were thoroughly blended therewith. Then, a conventional alkyl succinic acid rust inhibitor in an amount of 0.02 weight percent within a solvent carrier was blended therewith. Then, 0.02 weight percent of benzotriazole was thoroughly blended therewith along with a conventional dye and antifoam agent in an amount of parts per million and 15 parts per million, respectively. After the above ingredients were thoroughly blended together to form a homogeneous mixture of materials, the functional fluid was thoroughly tested to give the following properties:
TABLE I.TYPICAL PROPERTIES Appearance Blue Specific gravity, 60 F. (ASTM D-l298) 1.011 Refractive index, 77 F. (ASTM D-1218) 1.4476 Viscosity:
Cs. at 210 F. 3.40 Cs. at 100 F. 10.22 Cs. at 65 F. 1550 (ASTM D-445). Viscosity index, calc. 216 (ASTM D-2270) tables 264 Pour point F. (ASTM D-9'7) Below 80 Neutralization No. mgs. KOH/gm. (ASTM D-974) 0.13 Water, wt. percent (ASTM D-1744) 0.10
TABLE II.FIRE PROPERTIES Flash point, F. (ASTM D-92) 340 Fire point, F. (ASTM D-92) 380 Autogenous ignition temperature, F. (ASTM D-286) 1025 Manifold ignition, F. 1300 TABLE III.CHEMICAL STABILITY Hydrolytic stability-48 hours at 200 F. (Fed. Test Method Std. No. 791a Method 3457) TABLE V.TIIERMAL STABILITY (Fed. Test Method Std. No. 791a Method 2508) (24 hours at 400 F.)
Viscosity change cs. at 100 F -0.65 NN change, mg. KOH/gm +5.34
TABLE VIE-SHEAR STABILITY Viscosity loss at 100 -F. (percent), shear time:
TABLE VIII.FOAMING TENDENCIES (ASTM D-892) Sequence I, 75 F.:
Tendency, ml 0 Stability, sec. Sequence II, 200 F.:
Tendency, ml 10 Stability, sec. 5 Sequence III, 75 F.:
Tendency, ml. 0
Stability, sec.
TABLE IX.--LUBRICITY (a) Four Ball (ASTM D-2266) 600 r.p.m., 1 hour at 167 F., steel on steel:
Mm. scar, 1 kg. load 0.15
Mm. scar, 40 kg. load 0.60 Steel on bronze:
Mm. scar, 1 kg. load 0.20
Mm. scar, 40 kg. load 0.70 (b) Falex extreme pressure (Seizure) Load, lbs. 1900 Torque, in.-lbs 50 TABLE X.--COMPATIBILITY WITH ELASTOMERS (Fed. Test Method Std. No. 791a Method 3604) Ethylene propylene rubber percent-swell 11.3 Butyl rubber, percent swell 8.0
Example 2 The thermal stability of a conventional functional fluid was tested and compared to the fluid of the present invention. Thus, a sample of a commercially available material was obtained and tested in accordance with the procedures outlined in Table V. The active material was octyl diphenylphosphate. The viscosity change measured in centistrokes at 100 F. was 0.25 while the neutralization number change measured in milligrams potassium hydroxide per gram was +7.57. A comparison to the thermal stability as indicated in Table 5 of Example 1 illustrates the superiority of the fluid of the present invention.
While specific details of the present invention have been set forth herein, it is understood that variations in amounts and the addition of other materials are within the scope of the invention. Specifically, up to 5% water may be added if desired.
What is claimed is:
1. A composition useful as a base stock in hydraulic fluids which consists essentially of at least 50 to about by weight of a tiralkyl phosphate selected from the group consisting of tripropyl phosphate, tributyl phosphate, trihexyl phosphate, trioctyl phosphate, dipropyl octyl phosphate, dibutyl octyl phosphate, dipropyl hexyl phosphate, dihexyl octyl phosphate, dihexyl propyl phosphate, propyl butyl octyl phosphate and mixtures thereof, and a mixture of from about 5 to about 25% by weight of tricresyl phosphate and from about 5 to about 25% by weight of trixylenyl phosphate, said mixture of tricresyl and trixylenyl phosphates having a viscosity of between about 145 to about 230 Saybolt Universal Seconds measured at 100 F.
2- The base stock of claim 1 in which said trialkyl phosphate is present in an amount from about 65 to about 75% by weight and said tricresyl and trixylenyl phosphates are each present in amounts from about to about by weight.
3. A hydraulic fluid consisting essentially of the base stock in accordance with claim 1 and additionally containing from about 5 to about by weight of a polymethacrylate viscosity index improver, from about 0.01 to about 0.5% by weight of an alkyl succinic acid and from about 0.001 to about 0.5 of a corrosion inhibitor selected from the group consisting of benzotriazole and quinizarin.
4. The hydraulic fluid of claim 3 additionally containing between about 5 to about 20 parts per million of a dye and between about 5 to about parts per million of an antifoaming agent.
5. The hydraulic fluid of claim 3 additionally containing up to about 5% by weight water.
6. A composition useful as a hydraulic fluid consisting essentially of from about to about by weight of tributyl phosphate, a mixture of from about 5 to about 6 15 tricresyl phosphate and from about 5 to about 15 trixylenyl phosphate, said mixture of tricresyl and trixylenyl phosphates having a viscosity between about 145 to about 230 Saybolt Universal Seconds measured to F., from about 5 to about 20% by weight of a polymethacrylate viscosity index improver containing an alkyl moiety having up to 20 carbon atoms, from about 0.001 to about 0.5 by weight of benzot'riazole, from between about 5 to about 20 parts per million of a dye, and between about 5 to about 50 parts per million of an antifoaming agent.
References Cited UNITED STATES PATENTS 2,470,792 5/ 1949 Schlesinger 252--78 2,549,270 4/1951 Watson 252-78 2,636,861 4/1953 Watson 252-78 2,862,886 12/ 1958 Davies et a1. 25278 3,231,587 1/1966 Reuse 260346.8 3,413,227 11/1968 Howard at al 25251.5
LEON D. ROSDOL, Primary Examiner H. A. PITLICK, Assistant Examiner US. Cl. X.R. 252-49.9
US77675A 1967-09-06 1970-10-05 Functional fluid composition Expired - Lifetime US3707500A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US66573667A 1967-09-06 1967-09-06
US7767570A 1970-10-05 1970-10-05

Publications (1)

Publication Number Publication Date
US3707500A true US3707500A (en) 1972-12-26

Family

ID=26759543

Family Applications (1)

Application Number Title Priority Date Filing Date
US77675A Expired - Lifetime US3707500A (en) 1967-09-06 1970-10-05 Functional fluid composition

Country Status (1)

Country Link
US (1) US3707500A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3931022A (en) * 1974-09-16 1976-01-06 Texaco Inc. Turbine lubricant and method
US4252600A (en) * 1979-10-22 1981-02-24 International Telephone And Telegraph Corporation Ultrasonic welding apparatus for making a bellows
US4298489A (en) * 1977-02-25 1981-11-03 Kao Soap Co., Ltd. Phosphate ester-based fire resistant hydraulic fluid containing an aliphatic polyester
US4645615A (en) * 1986-02-27 1987-02-24 Fmc Corporation Fire-resistant hydraulic fluid
US5817606A (en) * 1996-08-08 1998-10-06 Rohm And Haas Company Viscosity index improving additives for phosphate ester-containing hydraulic fluids
WO2018108869A1 (en) 2016-12-14 2018-06-21 Evonik Oil Additives Gmbh Use of polyesters as viscosity index improvers for aircraft hydraulic fluids

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3931022A (en) * 1974-09-16 1976-01-06 Texaco Inc. Turbine lubricant and method
US4298489A (en) * 1977-02-25 1981-11-03 Kao Soap Co., Ltd. Phosphate ester-based fire resistant hydraulic fluid containing an aliphatic polyester
US4252600A (en) * 1979-10-22 1981-02-24 International Telephone And Telegraph Corporation Ultrasonic welding apparatus for making a bellows
US4645615A (en) * 1986-02-27 1987-02-24 Fmc Corporation Fire-resistant hydraulic fluid
US5817606A (en) * 1996-08-08 1998-10-06 Rohm And Haas Company Viscosity index improving additives for phosphate ester-containing hydraulic fluids
WO2018108869A1 (en) 2016-12-14 2018-06-21 Evonik Oil Additives Gmbh Use of polyesters as viscosity index improvers for aircraft hydraulic fluids
US11339346B2 (en) 2016-12-14 2022-05-24 Evonik Operations Gmbh Use of polyesters as viscosity index improvers for aircraft hydraulic fluids

Similar Documents

Publication Publication Date Title
US2411159A (en) Lubricant
US2636861A (en) Hydraulic fluid
US3637507A (en) Aircraft hydraulic fluid and method of controlling acid buildup therein with acid acceptor
US3941708A (en) Hydraulic fluid antioxidant system
US2801968A (en) Jet turbine lubricant
US3956154A (en) Hydraulic fluid system
US3707500A (en) Functional fluid composition
US2956951A (en) Water base lubricant containing dimethyl sulfoxide
US2566623A (en) Hydraulic fluid composition
US2659699A (en) Hydraulic fluid of polyhydric alcohol and trialkyl phosphate
US2944973A (en) Di-ester fluids with improved water tolerance
US2839468A (en) Jet turbine lubricant composition
US3935116A (en) Functional fluid compositions
US2836565A (en) Lubricating compositions
US3468802A (en) Corrosion inhibited hydraulic fluids
US2934501A (en) Fire-resistant functional fluid and lubricant composition
US3432437A (en) Fire resistant hydraulic fluid and lubricant compositions
US2435950A (en) Hydraulic fluids
NO124315B (en)
US3136726A (en) Fire-resistant hydraulic fluid and lubricant
US3793207A (en) Fire-resistant hydraulic fluid
US3074889A (en) Uninflammable hydraulic fluids
US3849324A (en) Functional fluids
KR20110119322A (en) Flame retardant hydraulic oil composition
US4007123A (en) Fire resistant functional fluid compositions

Legal Events

Date Code Title Description
AS Assignment

Owner name: AKZO AMERICA INC., A CORP. OF DE, NEW YORK

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:STAUFFER CHEMICAL COMPANY;REEL/FRAME:005080/0328

Effective date: 19890213