EP2307532B1 - Use as an antiwear hydraulic fluid composition - Google Patents

Use as an antiwear hydraulic fluid composition Download PDF

Info

Publication number
EP2307532B1
EP2307532B1 EP09803603.1A EP09803603A EP2307532B1 EP 2307532 B1 EP2307532 B1 EP 2307532B1 EP 09803603 A EP09803603 A EP 09803603A EP 2307532 B1 EP2307532 B1 EP 2307532B1
Authority
EP
European Patent Office
Prior art keywords
use according
composition
alkyl
detergent additive
hydraulic fluid
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.)
Active
Application number
EP09803603.1A
Other languages
German (de)
French (fr)
Other versions
EP2307532A4 (en
EP2307532A2 (en
Inventor
Rawls H. Frazier Jr.
Patrice Hamel
Nicolas Denieulle
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.)
Chevron Oronite SAS
Original Assignee
Chevron Oronite SAS
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 Chevron Oronite SAS filed Critical Chevron Oronite SAS
Priority to EP13180664.8A priority Critical patent/EP2669355A1/en
Publication of EP2307532A2 publication Critical patent/EP2307532A2/en
Publication of EP2307532A4 publication Critical patent/EP2307532A4/en
Application granted granted Critical
Publication of EP2307532B1 publication Critical patent/EP2307532B1/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

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
    • C10M159/00Lubricating compositions characterised by the additive being of unknown or incompletely defined constitution
    • C10M159/12Reaction products
    • C10M159/20Reaction mixtures having an excess of neutralising base, e.g. so-called overbasic or highly basic products
    • C10M159/22Reaction mixtures having an excess of neutralising base, e.g. so-called overbasic or highly basic products containing phenol radicals
    • 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
    • C10M2201/18Ammonia
    • 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
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/10Petroleum or coal fractions, e.g. tars, solvents, bitumen
    • C10M2203/1006Petroleum or coal fractions, e.g. tars, solvents, bitumen used as base material
    • 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
    • C10M2207/026Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings with tertiary alkyl groups
    • 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
    • C10M2207/028Overbased 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
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/26Overbased carboxylic acid salts
    • C10M2207/262Overbased carboxylic acid salts derived from hydroxy substituted aromatic acids, e.g. salicylates
    • 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
    • C10M2207/281Esters of (cyclo)aliphatic monocarboxylic 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
    • C10M2207/287Partial esters
    • C10M2207/289Partial esters containing free hydroxy groups
    • 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
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/10Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/101Condensation polymers of aldehydes or ketones and phenols, e.g. Also polyoxyalkylene ether derivatives 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
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/10Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/103Polyethers, i.e. containing di- or higher polyoxyalkylene groups
    • C10M2209/104Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing two carbon atoms 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
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • 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
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/04Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
    • C10M2219/044Sulfonic acids, Derivatives thereof, e.g. neutral 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
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/08Thiols; Sulfides; Polysulfides; Mercaptals
    • C10M2219/082Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
    • C10M2219/087Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Derivatives thereof, e.g. sulfurised phenols
    • C10M2219/089Overbased 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
    • 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
    • C10M2223/045Metal containing thio derivatives
    • 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
    • C10N2020/00Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
    • C10N2020/01Physico-chemical properties
    • C10N2020/02Viscosity; Viscosity index
    • 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
    • C10N2030/12Inhibition of corrosion, e.g. anti-rust agents or anti-corrosives
    • 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
    • C10N2030/24Emulsion properties
    • 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
    • C10N2030/40Low content or no content compositions
    • 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
    • C10N2030/52Base number [TBN]
    • 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
    • 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
    • C10N2070/00Specific manufacturing methods for lubricant compositions
    • C10N2070/02Concentrating of additives

Definitions

  • the present invention relates to detergents utilized in antiwear hydraulic fluid compositions.
  • the present invention relates to the use of a composition as an antiwear hydraulic fluid which can be useful for certain mobile equipment applications (e.g., hydraulic fluids for construction equipment).
  • Hydraulic fluids need to protect equipment from rust. To achieve this they are formulated with rust inhibitors. Typical rust inhibitors are metal sulfonates or succinic acid derivatives. Hydraulic fluids are also typically designed to separate readily from water (demulsify). Often, metallic rust inhibitors act to improve the demulsifying characteristics of the fluids.
  • Japanese Patent Publication No. JP5311187A describes a composition containing (A) a base fluid of a sulfur content of up to 100 ppm, (B) 0.2-1 wt. % of zinc dithiophosphate, (C) 0.2-1 wt. % of an alkaline earth metal salt of salicylic acid and (D) 0.001-0.5 wt. % of a water-separating agent.
  • WO0063325 describes a hydraulic fluid comprising lubricant base fluid, 0.001-5 wt.% of magnesium salicylate and 0.01-8 wt.% of zinc dithiophosphate.
  • the hydraulic fluid composition also comprises a rust inhibitor.
  • This publication also discloses the combination of a calcium salicylate, zinc dithiophosphate, and a rust inhibitor.
  • compositions incorporating a metal salt of an alkyl salicylate, zinc dithiophosphate, and a rust inhibitor typically include demulsifiers to facilitate the separation of water from the fluid.
  • demulsifiers to facilitate the separation of water from the fluid.
  • fluids with enhanced detergent and dispersant characteristics e.g., so called HLPD and HVLPD fluids as defined by the German DIN 51 502 standard
  • hydraulic fluids for certain mobile equipment applications e.g., hydraulic fluids for Caterpillar equipment, building machinery, excavators, hydraulic hoists, lifting platforms, presses, and the like
  • Engine fluids which are typically formulated with large amounts of dispersants, are a way to provide these emulsifying characteristics. Hydraulic fluids with certain sulfonate detergents can also have these characteristics.
  • US 2006/111252 discloses an emulsifier blend which includes at least one alkali metal sulfonate and at least one alkali metal alkyl salicylate.
  • the emulsifier blend can be combined with a lubricant oil to provide a water-miscible lubricating oil concentrate capable of forming a stable aqueous emulsion when added to an aqueous medium.
  • One aspect of this invention is the use of a composition comprising a major amount of a base fluid of lubricating viscosity and a minor amount of at least one oil soluble detergent additive; as an antiwear hydraulic fluid.
  • This detergent additive comprises a non-sulfurized calcium salt of an alkyl-substituted hydroxybenzoic acid.
  • the composition has a Carboxylate Index of greater than 0.084.
  • the antiwear hydraulic fluid composition is able to able to achieve an emulsion of 0 ml of fluid, 0 ml of water and 80 ml of emulsion (abbreviated 0-0-80) for 30 minutes or more, preferably 40 minutes or more in the ASTM D 1401 water separability test method.
  • the hydraulic fluid composition is able to achieve a "pass" result in the ASTM D 665 rust inhibition test method.
  • salts as described above exhibit excellent emulsifying and rust inhibition characteristics. This combined performance is unexpected when compared to other detergents.
  • One advantage of the present invention is the reduction or removal of conventional rust inhibitors, such as metallic naphthalene sulfonic acid salts, (e.g., NA-SUL® from King Industries).
  • Antiwear hydraulic fluids are used in hydraulic systems to prevent wear in mechanical equipment in hydraulic systems, for example, to prevent wear on moving metal on metal surfaces, such as steel on steel surfaces. Antiwear hydraulic fluids are useful, for example, in preventing wear in a variety of pumps, including but not limited to, vane pumps, piston pumps, and gear pumps, commonly used in hydraulic systems. Antiwear hydraulic fluids also provide protection for other parts of the hydraulic system such as motors, actuators, and pistons. Antiwear hydraulic fluids typically contain antiwear additves or extreme pressure agents, such as zinc dialkyl dithiophosphate.
  • the antiwear hydraulic fluid of the present invention exhibits several performance features in addition to antiwear protection, in particular emulsification and rust protection.
  • the antiwear hydraulic fluid of the present invention exhibits good oxidation stability, good filterability, good thermal stability, low internal friction, and good hydrolytic stability.
  • the base oil of lubricating viscosity employed in the present invention may be mineral oil or synthetic oils.
  • a base oil having a viscosity of at least 10 cSt (mm 2 /s) at 40 C. and a pour point below 20 C., preferably at or below 0 C. is desirable.
  • the base oils may be derived from synthetic or natural sources.
  • Mineral oils for use as the base oil in this invention include, for example, paraffinic, naphthenic and other fluids that are ordinarily used in lubricating oil compositions.
  • Synthetic oils include, for example, both hydrocarbon synthetic oils and synthetic esters and mixtures thereof having the desired viscosity.
  • Hydrocarbon synthetic oils may include, for example, liquid polymers having the proper viscosity prepared from the polymerization of ethylene or higher alpha olefins (polyalphaolefin or PAO), or from hydrocarbon synthesis procedures using carbon monoxide and hydrogen gases such as in a Fisher-Tropsch process.
  • polyalphaolefin or PAO polyalphaolefin
  • PAO polyalphaolefin
  • the hydrogenated liquid oligomers of C 6 to C 12 alpha olefins such as 1-decene trimer.
  • alkyl benzenes of proper viscosity such as didodecyl benzene, can be used.
  • Useful synthetic esters include the esters of monocarboxylic acids and polycarboxylic acids, as well as mono-hydroxy alkanols and polyols.
  • Typical examples are didodecyl adipate, pentaerythritol tetracaproate, di-2-ethylhexyl adipate, dilaurylsebacate, and the like.
  • Complex esters prepared from mixtures of mono and dicarboxylic acids and mono and dihydroxy alkanols can also be used.
  • Blends of mineral oils with synthetic oils are also useful. For example, blends of 10 wt % to 25 wt % hydrogenated 1-decene trimer with 75 wt % to 90 wt % 150 SUS (100F.) mineral oil make excellent lubricating oil bases.
  • the base oil of the present invention is present in a "major amount.”
  • a “major amount” of a base oil of lubricating viscosity refers to a concentration of the oil within the hydraulic fluid composition of at least about 40 wt %.
  • "a major amount” of a base oil of lubricating viscosity refers to a concentration of the oil within the hydraulic fluid composition of at least about 50 wt %, at least about 60 wt %, at least about 70 wt %, at least about 80 wt %, or at least about 90 wt %.
  • composition employed in the present invention comprises at least one suitable detergent additive that is oil soluble.
  • the detergent additive comprises a non-sulfurized calcium salt of an alkyl-substituted hydroxybenzoic acid.
  • the Total Base Number (“TBN”) of the detergent additive is typically less than 200 mg KOH/g, and preferably less than 160 mg KOH/g.
  • Total Base Number or “TBN” refers to the equivalent number of milligrams of KOH needed to neutralize 1 gram of a product. Therefore, a high TBN reflects strongly overbased products and, as a result, a higher base reserve for neutralizing acids.
  • the TBN of a product can be determined by ASTM Standard No. D 2896 or equivalent procedure.
  • An overbased detergent can be any detergent in which the TBN of the additive has been increased by a process such as the addition of a base source (such as lime) and an acidic overbasing compound (such as carbon dioxide).
  • At least 75% (such as at least 80%, at least 85%, at least 90%, at least 95%, or at least 99%) of the alkyl groups contained within the detergent (such as the alkyl groups of a carboxylate-containing detergent, or of an alkyl-substituted hydroxybenzoic acid) to be C 14 or greater, such as C 14 -C 40 , C 14 -C 35 , C 14 -C 30 , or C 14 -C 25 ,.
  • At least 75% (such as at least 80%, at least 85%, at least 90%, at least 95%, or at least 99%) of the alkyl groups contained within the detergent, with the remainder (such as 25% or less, about 20% or less, 15% or less, 10% or less, 5% or less, or even 1 % or less) of the alkyl groups contained within the detergent to be C 8 or greater (such as C 8 -C 14 , C 10 -C 14 , or even C 12 -C 14 ).
  • the detergent comprises a calcium salt of an alkyl-substituted hydroxybenzoic acid that is derived from an alkyl-substituted hydroxybenzoic acid in which the alkyl groups are the residue of normal alpha-olefins containing at least 90% C 20 or greater normal alpha-olefins.
  • the detergent comprises a calcium salt (e.g., an overbased salt) of an alkyl-substituted hydroxybenzoic acid.
  • the detergent is in a mixture with an overbased salt (such as an overbased alkaline earth metal salt) of an alkyl-substituted phenol.
  • the detergent is in a mixture with an overbased salt of an alkyl-substituted phenol, in combination or mixture with a non-overbased salt of one or more of: an alkyl-substituted hydroxybenzoic acid and an alkyl-substituted phenol.
  • the composition comprises one or more detergents comprising an overbased calcium salt of an alkyl-substituted hydroxybenzoic acid and no other overbased salts (other than the salt of the detergent).
  • the detergent additive in this regard, can comprise any suitable concentration of anion (e.g., organic anion) associated with the carboxylate salt (or salt of the alkyl-substituted hydroxybenzoic acid).
  • Suitable detergents which may be used in combination with the non-sulfurized calcium salt of an alkyl-substituted hydroxybenzoic acid include alkyl or alkenyl aromatic sulfonates, borated sulfonates, sulfurized or unsulfurized metal salts of multi hydroxy alkyl or alkenyl aromatic compounds, alkyl or alkenyl hydroxy aromatic sulfonates, sulfurized or unsulfurized alkyl or alkenyl naphthenates, metal salts of alkanoic acids, metal salts of an alkyl or alkenyl multiacid, and chemical and physical mixtures thereof.
  • suitable detergent additives include metal sulfonates, salicylates, phosphonates, thiophosphonates and combinations thereof.
  • the metal can be any metal suitable for making sulfonate, salicylate or phosphonate detergents.
  • suitable metals include alkali metals, alkaline metals and transition metals. In some embodiments, the metal is Ca, Mg, Ba, Sr, K, Na, Li or the like.
  • the detergent additive employed in the present invention is generally soluble in oil as characterized by the following test: A mixture of a 600N oil and the additive at a content of 10% by weight with respect to the total weight of the mixture is centrifuged at a temperature of 60 C and for 30 minutes, the centrifugation being carried out under the conditions stipulated by the standard ASTM D2273 (it should be noted that centrifugation is carried out without dilution, i.e. without adding solvent); immediately after centrifugation, the volume of the deposit which forms is determined; if the deposit is less than 0.05% v/v (volume of the deposit with respect to the volume of the mixture), the product is considered as soluble in oil.
  • the aforementioned oil soluble detergent additive in the antiwear hydraulic fluid composition of the present invention has a TBN typically less than 200 mg KOH/g, and preferably less than 160 mg KOH/g.
  • the concentration of the oil soluble detergent additive itself will generally range from an amount of between about 0.05 wt % to about 0.3 wt%, and preferably about 0.07 wt% to about 0.25 wt %, based on the total weight of the hydraulic fluid composition.
  • the detergent additive of the present invention is present in a "minor amount.”
  • a “minor amount” of detergent additive refers to a concentration of the detergent additive within the hydraulic fluid composition of less than about 60 wt %.
  • a “minor amount” of detergent additive refers to a concentration of the detergent additive within the hydraulic fluid composition of less than about 50 wt%, of less than about 30 wt %, of less than about 10 wt %, of less than about 1 wt %, or of less than about 0.5 wt %.
  • detergents help control varnish, ring zone deposits, and rust by keeping insoluble particles in colloidal suspension.
  • Metal-containing (or ash-forming detergents) function both as detergents to control deposits, and as acid neutralizers or rust inhibitors, thereby reducing wear and corrosion and extending equipment life.
  • Detergents generally comprise a polar head with a long hydrophobic tail; with the polar head comprising a metal salt of an acidic organic compound.
  • the salts may contain a substantially stoichiometric amount of the metal in which case they are usually described as normal or neutral salts.
  • the detergent additives in the antiwear hydraulic fluid composition of the present invention can be characterized by the amount of potassium hydroxide equivalent to the amount of alkyl-substituted hydroxybenzoate (also referred to herein as a salt of an alkyl substituted hydroxybenzoic acid), or a sulfurized derivative thereof, present in the detergent expressed as mg KOH/g detergent and referred to as the Carboxylate Index (CI).
  • CI Carboxylate Index
  • the alkyl-substituted hydroxybenzoate detergent additive is dissolved in an organic solvent and washed three times with equal volumes of a dilute, strong acid solution.
  • the aqueous layers are collected.
  • the combined aqueous layers are washed with an organic solvent.
  • the aqueous layer is removed and the organic layers are combined and subsequently washed with distilled water.
  • the aqueous layer is decanted.
  • the acidified extract is treated with pyridine and titrated with dilute, standardized base.
  • Cl of antiwear hydraulic fluid composition Cl of alkyl - substituted hydroxybenzoate detergent x wt . % alkyl - substituted hydroxybenzoate detergent in fluid
  • the CI of the antiwear hydraulic fluid composition is greater than 0.084, preferably greater than 0.10, and more preferably greater than 0.12.
  • the CI of the antiwear hydraulic fluid composition is greater than 0.034, and more preferably greater than 0.04.
  • the oil soluble detergent additive of the present invention can be employed as a concentrate which will typically contain a sufficient amount of an organic liquid diluent and the oil soluble detergent additive employed in the present invention.
  • the concentrates contain sufficient organic liquid diluent to make them easy to handle during shipping and storage.
  • the concentrate will contain from about 10 wt % to 90 wt %; preferably, from about 20 wt % to 70 wt %; and more preferably, from about 20 wt % to 35 wt %, of a compatible organic liquid diluent.
  • Suitable organic liquid diluents which can be used include, for example, paraffinic base oils such as solvent refined 100N, e.g., Cit-Con 100N, and hydrotreated 100N, e.g., Chevron 100N, and the like.
  • the organic liquid diluent preferably has a viscosity of from about 1 to 20 cSt at 100C. From about 10 wt % to 90 wt %; preferably, from about 30 wt % to 80 wt % of the concentrate is the oil soluble additive employed in the present invention.
  • additive components are examples of some of the components that can be favorably employed in the present invention. These examples of additives are provided to illustrate the present invention, but they are not intended to limit it:
  • a base-line formulation was prepared and used for assessing the performance of the detergent in Example 1 in the ASTM D 1401 water separability test.
  • the base-line formulation contained 0.31 wt. % of a zinc dialkyldithiophosphate, 0.15 wt. % of a hindered phenol antioxidant, 0.044 wt. % of a succinate ester dispersant, 0.044 wt. % of a fatty ester friction modifier, 0.013 wt. % of an arylpolyol demulsifier and 0.008 wt. % of a foam inhibitor in a base fluid containing Shell HVI basestocks. All finished fluids in these Examples are ISO VG 46 with 8 wt. % of a polyalkyl methacrylate viscosity index improver.
  • An antiwear hydraulic fluid composition was prepared consisting of the baseline formulation above with the addition of 0.225 wt. % of an overbased calcium alkyl-substituted hydroxybenzoate detergent wherein at least 90% of the alkyl groups are C 20 or greater and 0.06 wt. % of the succinate ester dispersant.
  • the overbased calcium alkyl-substituted hydroxybenzoate detergent was prepared according to the method described in Example 1 of US Patent Application 2007/0027043 and has a calcium content of 5.35 wt. %, a TBN of 150 and a CI of 56.
  • An antiwear hydraulic fluid composition was prepared in accordance with the formulation of Example 1 except that 0.01 wt. % of a linear alcohol ethoxylate emulsifier and 0.16 wt% zinc dialkyl dithiophosphate was added.
  • An antiwear hydraulic fluid composition was prepared consisting of the base-line formulation above with the addition of 0.041 wt. % of an overbased, sulfurized alkyl-substituted hydroxybenzoate-containing detergent, 0.024 wt. % of an overbased calcium phenate, 0.027 wt. % of a naphthalene sulfonic acid zinc salt rust inhibitor and 0.008 wt. % of a phenolic resin demulsifier.
  • the overbased, sulfurized carboxylate-containing detergent was prepared according to the method described in Example 16 of US Patent Number 5808145 and has a calcium content of 9.3 wt. %, a sulfur content of 2.4 wt. %, a TBN of 260 and a CI of 28.
  • An antiwear hydraulic fluid composition was prepared consisting of the baseline formulation above with the addition of 0.075 wt. % of the 56 CI overbased calcium alkyl-substituted hydroxybenzoate as described in Example 1.
  • An antiwear hydraulic fluid composition was prepared in accordance with the formulation of Comparative Example 2 except that 0.06 wt. % of the succinate ester dispersant was added.
  • An antiwear hydraulic fluid composition was prepared consisting of the baseline formulation above with the addition of 0.15 wt. % of the 56 CI overbased calcium alkylhydroxybenzoate as described in Example 1.
  • An antiwear hydraulic fluid composition was prepared in accordance with the formulation of Comparative Example 4 except that 0.06 wt. % of the succinate ester dispersant was added.
  • the water separability of antiwear hydraulic fluids is characterized in the ASTM D 1401 test method.
  • a 40 mL volume of the sample material was emulsified with a 40 mL volume of distilled water by stirring the combined liquids in a graduated cylinder at 54°C for 5 minutes.
  • the separation of the emulsion into organic and aqueous layers was characterized by monitoring the relative volumes of the respective fluid, water and emulsion layers after cessation of stirring. Results are set forth below in Table 1 as the respective mL fluid-mL water-mL emulsion observed at minutes after cessation of stirring.
  • a base-line formulation was prepared and used for assessing the performance of various detergents in the ASTM D 665 rust prevention test.
  • the base-line formulation contained 0.31 wt. % of a zinc dialkyldithiophosphate, 0.15 wt. % of a hindered phenol antioxidant, 0.044 wt. % of a succinate ester dispersant, 0.044 wt. % of a fatty ester friction modifier, 0.013 wt. % of an arylpolyol demulsifier, 0.008 wt. % of a phenolic resin demulsifier, 0.2 wt. % of a pour point depressant and 0.008 wt. % of a foam inhibitor in a base oil containing ExxonMobil AP/E CORE ® basestocks. All finished fluids in these Examples are ISO VG 68.
  • An antiwear hydraulic fluid composition was prepared consisting of the baseline formulation above with the addition of 0.075 wt. % of the 56 CI overbased calcium alkyl-substituted hydroxybenzoate detergent as described in Example 1.
  • An antiwear hydraulic fluid composition was prepared consisting of the baseline formulation above with the addition of 0.041 wt. % of the 28 CI overbased, sulfurized, alkyl-substituted hydroxybenzoate-containing detergent as described in Comparative Example 1, 0.024 wt. % of an overbased calcium phenate and 0.027 wt. % of a naphthalene sulfonic acid zinc salt rust inhibitor.
  • An antiwear hydraulic fluid composition was prepared consisting of the baseline formulation above with the addition of 0.067 wt. % of an overbased calcium alkyl-substituted hydroxybenzoate detergent wherein at least 90% of the alkyl groups are C 14 -C 18 .
  • the detergent has a TBN of 168 and a CI of 51.
  • An antiwear hydraulic fluid composition was prepared consisting of the baseline formulation above with the addition of 0.049 wt. % of an overbased calcium alkyl-substituted hydroxybenzoate detergent wherein at least 90% of the alkyl groups are C 20 -C 28 .
  • the detergent has a TBN of 230 and a CI of 46.
  • An antiwear hydraulic fluid composition was prepared consisting of the baseline formulation above with the addition of 0.035 wt. % of an overbased calcium alkyl-substituted hydroxybenzoate detergent wherein at least 90% of the alkyl groups are C 20 -C 28 .
  • the detergent has a TBN of 325 and a CI of 36.
  • An antiwear hydraulic fluid composition was prepared consisting of the baseline formulation above with the addition of 0.032 wt. % of an overbased calcium alkyl-substituted hydroxybenzoate detergent wherein at least 90% of the alkyl groups are C 20 or greater.
  • the overbased calcium alkyl-substituted hydroxybenzoate detergent is prepared according to the method described in Example 1 of US Patent Application 2007/0027043 and has a calcium content of 12.5 wt. %, a TBN of 350 and a CI of 37.
  • Rust inhibition of antiwear hydraulic fluids was determined using ASTM D 665.
  • ASTM D 665 is directed at a test for determining the ability of fluid to aid in preventing the rusting of ferrous parts should water become mixed with the fluid.
  • Procedure B of ASTM D 665 was employed. In this test, a mixture of 300 mL of the test fluid is stirred with 30 mL of synthetic sea water at a temperature of 60°C with a cylindrical steel specimen completely immersed therein for 24 hours. The rust test results are reported as either a "pass” or a "fail.” The results are presented in Table 2. Table 2 not according to the invention Ex. 3 Comp. Ex. 6 Comp. Ex. 7 Comp. Ex. 8 Comp. Ex.
  • Example 3 demonstrated unexpected rust inhibiting performance when compared to other carboxylate/salicylate detergents (Comparative Examples 2-5) and also demonstrated unexpected rust inhibiting performance when compared to a formulation containing a rust inhibitor (Comparative Example 6).
  • the formulation of Example 3 advantageously does not require the addition of a rust inhibitor in order to pass this test.

Description

    Field of the Invention
  • The present invention relates to detergents utilized in antiwear hydraulic fluid compositions. In particular, the present invention relates to the use of a composition as an antiwear hydraulic fluid which can be useful for certain mobile equipment applications (e.g., hydraulic fluids for construction equipment).
  • Background of the Invention
  • Hydraulic fluids need to protect equipment from rust. To achieve this they are formulated with rust inhibitors. Typical rust inhibitors are metal sulfonates or succinic acid derivatives. Hydraulic fluids are also typically designed to separate readily from water (demulsify). Often, metallic rust inhibitors act to improve the demulsifying characteristics of the fluids.
  • Japanese Patent Publication No. JP5311187A describes a composition containing (A) a base fluid of a sulfur content of up to 100 ppm, (B) 0.2-1 wt. % of zinc dithiophosphate, (C) 0.2-1 wt. % of an alkaline earth metal salt of salicylic acid and (D) 0.001-0.5 wt. % of a water-separating agent.
  • International Application No. WO0063325 describes a hydraulic fluid comprising lubricant base fluid, 0.001-5 wt.% of magnesium salicylate and 0.01-8 wt.% of zinc dithiophosphate. The hydraulic fluid composition also comprises a rust inhibitor. This publication also discloses the combination of a calcium salicylate, zinc dithiophosphate, and a rust inhibitor.
  • The above publications describe compositions incorporating a metal salt of an alkyl salicylate, zinc dithiophosphate, and a rust inhibitor. Typically such compositions also include demulsifiers to facilitate the separation of water from the fluid. However, there is a need in some cases to have hydraulic fluids which emulsify, rather than demulsify, water. These include fluids with enhanced detergent and dispersant characteristics (e.g., so called HLPD and HVLPD fluids as defined by the German DIN 51 502 standard) and hydraulic fluids for certain mobile equipment applications (e.g., hydraulic fluids for Caterpillar equipment, building machinery, excavators, hydraulic hoists, lifting platforms, presses, and the like), wherein water separated from the fluid may not be adequately removed from the equipment leading to poor lubrication. Engine fluids, which are typically formulated with large amounts of dispersants, are a way to provide these emulsifying characteristics. Hydraulic fluids with certain sulfonate detergents can also have these characteristics.
  • US 2006/111252 discloses an emulsifier blend which includes at least one alkali metal sulfonate and at least one alkali metal alkyl salicylate. The emulsifier blend can be combined with a lubricant oil to provide a water-miscible lubricating oil concentrate capable of forming a stable aqueous emulsion when added to an aqueous medium.
  • Summary of the Invention
  • One aspect of this invention is the use of a composition comprising a major amount of a base fluid of lubricating viscosity and a minor amount of at least one oil soluble detergent additive; as an antiwear hydraulic fluid. This detergent additive comprises a non-sulfurized calcium salt of an alkyl-substituted hydroxybenzoic acid. The composition has a Carboxylate Index of greater than 0.084.
  • Optionally, at least 90% of the alkyl groups of said alkyl-substituted hydroxybenzoic acid are C14 or greater. Furthermore, optionally, the antiwear hydraulic fluid composition is able to able to achieve an emulsion of 0 ml of fluid, 0 ml of water and 80 ml of emulsion (abbreviated 0-0-80) for 30 minutes or more, preferably 40 minutes or more in the ASTM D 1401 water separability test method. Furthermore, optionally, the hydraulic fluid composition is able to achieve a "pass" result in the ASTM D 665 rust inhibition test method.
  • Surprisingly, we have found that salts as described above exhibit excellent emulsifying and rust inhibition characteristics. This combined performance is unexpected when compared to other detergents. One advantage of the present invention is the reduction or removal of conventional rust inhibitors, such as metallic naphthalene sulfonic acid salts, (e.g., NA-SUL® from King Industries).
  • Detailed Description of the Invention
  • Antiwear hydraulic fluids are used in hydraulic systems to prevent wear in mechanical equipment in hydraulic systems, for example, to prevent wear on moving metal on metal surfaces, such as steel on steel surfaces. Antiwear hydraulic fluids are useful, for example, in preventing wear in a variety of pumps, including but not limited to, vane pumps, piston pumps, and gear pumps, commonly used in hydraulic systems. Antiwear hydraulic fluids also provide protection for other parts of the hydraulic system such as motors, actuators, and pistons. Antiwear hydraulic fluids typically contain antiwear additves or extreme pressure agents, such as zinc dialkyl dithiophosphate.
  • The antiwear hydraulic fluid of the present invention exhibits several performance features in addition to antiwear protection, in particular emulsification and rust protection. In addition, the antiwear hydraulic fluid of the present invention exhibits good oxidation stability, good filterability, good thermal stability, low internal friction, and good hydrolytic stability.
  • Base Oil of Lubricating Viscosity
  • The base oil of lubricating viscosity employed in the present invention may be mineral oil or synthetic oils. A base oil having a viscosity of at least 10 cSt (mm2/s) at 40 C. and a pour point below 20 C., preferably at or below 0 C. is desirable. The base oils may be derived from synthetic or natural sources. Mineral oils for use as the base oil in this invention include, for example, paraffinic, naphthenic and other fluids that are ordinarily used in lubricating oil compositions. Synthetic oils include, for example, both hydrocarbon synthetic oils and synthetic esters and mixtures thereof having the desired viscosity. Hydrocarbon synthetic oils may include, for example, liquid polymers having the proper viscosity prepared from the polymerization of ethylene or higher alpha olefins (polyalphaolefin or PAO), or from hydrocarbon synthesis procedures using carbon monoxide and hydrogen gases such as in a Fisher-Tropsch process. Especially useful are the hydrogenated liquid oligomers of C6 to C12 alpha olefins such as 1-decene trimer. Likewise, alkyl benzenes of proper viscosity, such as didodecyl benzene, can be used. Useful synthetic esters include the esters of monocarboxylic acids and polycarboxylic acids, as well as mono-hydroxy alkanols and polyols. Typical examples are didodecyl adipate, pentaerythritol tetracaproate, di-2-ethylhexyl adipate, dilaurylsebacate, and the like. Complex esters prepared from mixtures of mono and dicarboxylic acids and mono and dihydroxy alkanols can also be used. Blends of mineral oils with synthetic oils are also useful. For example, blends of 10 wt % to 25 wt % hydrogenated 1-decene trimer with 75 wt % to 90 wt % 150 SUS (100F.) mineral oil make excellent lubricating oil bases.
  • The base oil of the present invention is present in a "major amount." A "major amount" of a base oil of lubricating viscosity refers to a concentration of the oil within the hydraulic fluid composition of at least about 40 wt %. In some embodiments, "a major amount" of a base oil of lubricating viscosity refers to a concentration of the oil within the hydraulic fluid composition of at least about 50 wt %, at least about 60 wt %, at least about 70 wt %, at least about 80 wt %, or at least about 90 wt %.
  • Detergent additive
  • As discussed previously, composition employed in the present invention comprises at least one suitable detergent additive that is oil soluble.
  • The detergent additive comprises a non-sulfurized calcium salt of an alkyl-substituted hydroxybenzoic acid.
  • The Total Base Number ("TBN") of the detergent additive is typically less than 200 mg KOH/g, and preferably less than 160 mg KOH/g. The term "Total Base Number" or "TBN" refers to the equivalent number of milligrams of KOH needed to neutralize 1 gram of a product. Therefore, a high TBN reflects strongly overbased products and, as a result, a higher base reserve for neutralizing acids. The TBN of a product can be determined by ASTM Standard No. D 2896 or equivalent procedure. An overbased detergent can be any detergent in which the TBN of the additive has been increased by a process such as the addition of a base source (such as lime) and an acidic overbasing compound (such as carbon dioxide).
  • It is preferred that for at least 75% (such as at least 80%, at least 85%, at least 90%, at least 95%, or at least 99%) of the alkyl groups contained within the detergent (such as the alkyl groups of a carboxylate-containing detergent, or of an alkyl-substituted hydroxybenzoic acid) to be C14 or greater, such as C14-C40, C14-C35, C14-C30, or C14-C25,. In some embodiments, at least 75% (such as at least 80%, at least 85%, at least 90%, at least 95%, or at least 99%) of the alkyl groups contained within the detergent, with the remainder (such as 25% or less, about 20% or less, 15% or less, 10% or less, 5% or less, or even 1 % or less) of the alkyl groups contained within the detergent to be C8 or greater (such as C8-C14, C10-C14, or even C12-C14). In one preferred embodiment, the detergent comprises a calcium salt of an alkyl-substituted hydroxybenzoic acid that is derived from an alkyl-substituted hydroxybenzoic acid in which the alkyl groups are the residue of normal alpha-olefins containing at least 90% C20 or greater normal alpha-olefins.
  • The detergent comprises a calcium salt (e.g., an overbased salt) of an alkyl-substituted hydroxybenzoic acid. In an embodiment, the detergent is in a mixture with an overbased salt (such as an overbased alkaline earth metal salt) of an alkyl-substituted phenol. In another embodiment, the detergent is in a mixture with an overbased salt of an alkyl-substituted phenol, in combination or mixture with a non-overbased salt of one or more of: an alkyl-substituted hydroxybenzoic acid and an alkyl-substituted phenol. In another embodiment, the composition comprises one or more detergents comprising an overbased calcium salt of an alkyl-substituted hydroxybenzoic acid and no other overbased salts (other than the salt of the detergent). The detergent additive, in this regard, can comprise any suitable concentration of anion (e.g., organic anion) associated with the carboxylate salt (or salt of the alkyl-substituted hydroxybenzoic acid).
  • Some non-limiting examples of other suitable detergents which may be used in combination with the non-sulfurized calcium salt of an alkyl-substituted hydroxybenzoic acid include alkyl or alkenyl aromatic sulfonates, borated sulfonates, sulfurized or unsulfurized metal salts of multi hydroxy alkyl or alkenyl aromatic compounds, alkyl or alkenyl hydroxy aromatic sulfonates, sulfurized or unsulfurized alkyl or alkenyl naphthenates, metal salts of alkanoic acids, metal salts of an alkyl or alkenyl multiacid, and chemical and physical mixtures thereof. Other non-limiting examples of suitable detergent additives include metal sulfonates, salicylates, phosphonates, thiophosphonates and combinations thereof. The metal can be any metal suitable for making sulfonate, salicylate or phosphonate detergents. Non-limiting examples of suitable metals include alkali metals, alkaline metals and transition metals. In some embodiments, the metal is Ca, Mg, Ba, Sr, K, Na, Li or the like.
  • The detergent additive employed in the present invention is generally soluble in oil as characterized by the following test: A mixture of a 600N oil and the additive at a content of 10% by weight with respect to the total weight of the mixture is centrifuged at a temperature of 60 C and for 30 minutes, the centrifugation being carried out under the conditions stipulated by the standard ASTM D2273 (it should be noted that centrifugation is carried out without dilution, i.e. without adding solvent); immediately after centrifugation, the volume of the deposit which forms is determined; if the deposit is less than 0.05% v/v (volume of the deposit with respect to the volume of the mixture), the product is considered as soluble in oil.
  • The aforementioned oil soluble detergent additive in the antiwear hydraulic fluid composition of the present invention has a TBN typically less than 200 mg KOH/g, and preferably less than 160 mg KOH/g. In the antiwear hydraulic fluid composition of the present invention, the concentration of the oil soluble detergent additive itself will generally range from an amount of between about 0.05 wt % to about 0.3 wt%, and preferably about 0.07 wt% to about 0.25 wt %, based on the total weight of the hydraulic fluid composition. Alternatively speaking, the detergent additive of the present invention is present in a "minor amount." A "minor amount" of detergent additive refers to a concentration of the detergent additive within the hydraulic fluid composition of less than about 60 wt %. In some embodiments, a "minor amount" of detergent additive refers to a concentration of the detergent additive within the hydraulic fluid composition of less than about 50 wt%, of less than about 30 wt %, of less than about 10 wt %, of less than about 1 wt %, or of less than about 0.5 wt %.
  • Generally speaking, detergents help control varnish, ring zone deposits, and rust by keeping insoluble particles in colloidal suspension. Metal-containing (or ash-forming detergents) function both as detergents to control deposits, and as acid neutralizers or rust inhibitors, thereby reducing wear and corrosion and extending equipment life. Detergents generally comprise a polar head with a long hydrophobic tail; with the polar head comprising a metal salt of an acidic organic compound. The salts may contain a substantially stoichiometric amount of the metal in which case they are usually described as normal or neutral salts.
  • Alkyl-substituted hydroxybenzoate detergent additive component
  • The detergent additives in the antiwear hydraulic fluid composition of the present invention can be characterized by the amount of potassium hydroxide equivalent to the amount of alkyl-substituted hydroxybenzoate (also referred to herein as a salt of an alkyl substituted hydroxybenzoic acid), or a sulfurized derivative thereof, present in the detergent expressed as mg KOH/g detergent and referred to as the Carboxylate Index (CI). Thus, a detergent additive with 56 mg KOH equivalent hydroxyphenyl carboxylate per gram of detergent would have a CI of 56 and would be referred to as 56 CI alkyl-substituted hydroxybenzoate.
  • Determination of the Carboxylate Index of a Detergent Additive and of an Antiwear Hydraulic Fluid Composition
  • The alkyl-substituted hydroxybenzoate detergent additive is dissolved in an organic solvent and washed three times with equal volumes of a dilute, strong acid solution. The aqueous layers are collected. The combined aqueous layers are washed with an organic solvent. The aqueous layer is removed and the organic layers are combined and subsequently washed with distilled water. The aqueous layer is decanted. The acidified extract is treated with pyridine and titrated with dilute, standardized base.
  • The Carboxylate Index (CI) of the detergent additive can then be calculated from the following formula: CI = V 1 x C x M W KOH / W
    Figure imgb0001

    wherein
    V1 is the volume required to reach the first end point in the titration curve;
    C is the concentration of the dilute, standardized base;
    MWKOH is the molecular weight of KOH; and
    W is the weight of the alkyl-substituted hydroxybenzoate detergent additive.
  • Once the CI of the detergent additive has been calculated, the CI of the antiwear hydraulic fluid composition can be readily determined from the amount of the alkyl-substituted hydroxybenzoate detergent additive present in the composition. This is expressed by the following formula: Cl of antiwear hydraulic fluid composition = Cl of alkyl - substituted hydroxybenzoate detergent x wt . % alkyl - substituted hydroxybenzoate detergent in fluid
    Figure imgb0002

    In one embodiment of the invention, the CI of the antiwear hydraulic fluid composition is greater than 0.084, preferably greater than 0.10, and more preferably greater than 0.12. In another embodiment of the invention, the CI of the antiwear hydraulic fluid composition is greater than 0.034, and more preferably greater than 0.04.
  • Concentrate Formulation
  • The oil soluble detergent additive of the present invention can be employed as a concentrate which will typically contain a sufficient amount of an organic liquid diluent and the oil soluble detergent additive employed in the present invention. The concentrates contain sufficient organic liquid diluent to make them easy to handle during shipping and storage. Typically, the concentrate will contain from about 10 wt % to 90 wt %; preferably, from about 20 wt % to 70 wt %; and more preferably, from about 20 wt % to 35 wt %, of a compatible organic liquid diluent. Suitable organic liquid diluents which can be used include, for example, paraffinic base oils such as solvent refined 100N, e.g., Cit-Con 100N, and hydrotreated 100N, e.g., Chevron 100N, and the like. The organic liquid diluent preferably has a viscosity of from about 1 to 20 cSt at 100C. From about 10 wt % to 90 wt %; preferably, from about 30 wt % to 80 wt % of the concentrate is the oil soluble additive employed in the present invention.
  • Other Additive Components
  • The following additive components are examples of some of the components that can be favorably employed in the present invention. These examples of additives are provided to illustrate the present invention, but they are not intended to limit it:
    1. 1. Dispersants: Alkenyl succinimides, alkenyl succinate esters, alkenyl succinimides modified with other organic compounds, alkenyl succinimides modified by posttreatment with ethylene carbonate or boric acid, pentaerythritols, phenate-salicylates and their post-treated analogs, alkali metal or mixed alkali metal, alkaline earth metal borates, dispersions of hydrated alkali metal borates, dispersions of alkaline-earth metal borates, polyamide ashless dispersants and the like or mixtures of such dispersants.
    2. 2. Anti-oxidants: Anti-oxidants reduce the tendency of mineral oils to deteriorate in service which deterioration is evidenced by the products of oxidation such as sludge and varnish-like deposits on the metal surfaces and by an increase in viscosity. Examples of anti-oxidants useful in the present invention include, but are not limited to, phenol type (phenolic) oxidation inhibitors, such as 4,4'-methylene-bis(2,6-di-tert-butylphenol), 4,4'-bis(2,6-di-tert-butylphenol), 4,4'-bis(2-methyl-6-tert-butylphenol), 2,2'-methylene-bis(4-methyl-6-tert-butyl-phenol), 4,4'-butylidene-bis(3-methyl-6-tert-butylphenol), 4,4'-isopropylidene-bis(2,6-di-tert-butylphenol), 2,2'-methylene-bis(4-me- thyl-6-nonylphenol), 2,2'-isobutylidene-bis(4,6-dimethylphenol), 2,2'-methylene-bis(4-methyl-6-cyclohexylphenol), 2,6-di-tert-butyl-4-methylphenol, 2,6-di-tert-butyl-4-ethylphenol, 2,6-di-tert-butylphenol, 2,4-dimethyl-6-tert-butyl-phenol, 2,6-di-tert-l-dimethylamino-p-cresol, 2,6-di-tert-4-(N,N'-dimethylamino- methylphenol), 4,4'-thiobis(2-methyl-6-tert-butylphenol), 2,2'-thiobis(4-methyl-6-tert-butylphenol), bis(3-methyl-4-hydroxy-5-tert--butylbenzyl)-sulfide, and bis(3,5-di-tert-butyl-4-hydroxybenzyl). Other types of oxidation inhibitors include alkylated diphenylamines (e.g., Irganox L-57 from Ciba-Geigy), metal dithiocarbamate (e.g., zinc dithiocarbamate), and methylenebis(dibutyldithiocarbamate).
    3. 3. Antiwear agents: As their name implies, these agents reduce wear of moving metallic parts. Examples of such agents include, but are not limited to, phosphates, phosphites, carbamates, esters, sulfur containing compounds, and molybdenum complexes.
    4. 4. Emulsifiers: Linear alcohol ethoxylates, including TERGITOL® 15-S-3 available from the Dow Chemical Company.
    5. 5. Demulsifiers: addition product of alkylphenol and ethylene oxide, polyoxyethylene alkyl ether, and polyoxyethylene sorbitan ester.
    6. 6. Extreme pressure agents (EP agents): zinc dialkyldithiophosphate (primary alkyl, secondary alkyl, and aryl type), sulfurized oils, diphenyl sulfide, methyl trichlorostearate, chlorinated naphthalene, fluoroalkylpolysiloxane, and lead naphthenate. A preferred EP agent is zinc dialkyl dithiophosphate (ZnDTP) as one of the co-additive components for the antiwear hydraulic fluid composition of the present invention, and is shown by the general formula:
      Figure imgb0003
      wherein, R1 and R2 are each a primary or secondary alkyl group having a carbon number of 1 to 18, and may be the same or different. The primary or secondary alkyl groups of R1 and R2 having a carbon number of 1 to 18, shown by the general formula, include methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, 2-ethyl hexyl, octyl, nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, and octadecyl. However, the preferable zinc dialkyl dithiophosphate for the antiwear hydraulic fluid of the present invention has a mixed alkyl group of primary and secondary alkyl groups having a carbon number of 3 to 12. A more preferable zinc dialkyl dithiophosphate for the antiwear hydraulic fluid composition of the present invention has a primary alkyl group having a carbon number of 3 to 12. The zinc dialkyl dithiophosphates having a mixed alkyl group of primary and secondary alkyl groups may be used either individually or in combination for the antiwear hydraulic fluid composition of the present invention. The zinc dialkyl dithiophosphate is incorporated at 0.01 to 0.50 wt. % as phosphorus derived therefrom, based on the whole composition, preferably 0.02 to 0.04 wt. %.
    7. 7. Friction modifiers: fatty alcohol, fatty acid, fatty ester amine, borated ester, and other esters.
    8. 8. Multifunctional additives: sulfurized oxymolybdenum dithiocarbamate, sulfurized oxymolybdenum organo phosphorodithioate, oxymolybdenum monoglyceride, oxymolybdenum diethylate amide, amine-molybdenum complex compound, and sulfur-containing molybdenum complex compound.
    9. 9. Viscosity index improvers: polymethacrylate type polymers, ethylene-propylene copolymers, styrene-isoprene copolymers, hydrogenated styrene-isoprene copolymers, polyisobutylene, and dispersant type viscosity index improvers.
    10. 10. Pour point depressants: polymethacrylate type polymers.
    11. 11. Foam inhibitors: alkyl methacrylate polymers and dimethyl silicone polymers
    Examples Emulsification Performance
  • A base-line formulation was prepared and used for assessing the performance of the detergent in Example 1 in the ASTM D 1401 water separability test. The base-line formulation contained 0.31 wt. % of a zinc dialkyldithiophosphate, 0.15 wt. % of a hindered phenol antioxidant, 0.044 wt. % of a succinate ester dispersant, 0.044 wt. % of a fatty ester friction modifier, 0.013 wt. % of an arylpolyol demulsifier and 0.008 wt. % of a foam inhibitor in a base fluid containing Shell HVI basestocks. All finished fluids in these Examples are ISO VG 46 with 8 wt. % of a polyalkyl methacrylate viscosity index improver.
  • Example 1
  • An antiwear hydraulic fluid composition was prepared consisting of the baseline formulation above with the addition of 0.225 wt. % of an overbased calcium alkyl-substituted hydroxybenzoate detergent wherein at least 90% of the alkyl groups are C20 or greater and 0.06 wt. % of the succinate ester dispersant. The overbased calcium alkyl-substituted hydroxybenzoate detergent was prepared according to the method described in Example 1 of US Patent Application 2007/0027043 and has a calcium content of 5.35 wt. %, a TBN of 150 and a CI of 56.
  • Example 2
  • An antiwear hydraulic fluid composition was prepared in accordance with the formulation of Example 1 except that 0.01 wt. % of a linear alcohol ethoxylate emulsifier and 0.16 wt% zinc dialkyl dithiophosphate was added.
  • Comparative Example 1
  • An antiwear hydraulic fluid composition was prepared consisting of the base-line formulation above with the addition of 0.041 wt. % of an overbased, sulfurized alkyl-substituted hydroxybenzoate-containing detergent, 0.024 wt. % of an overbased calcium phenate, 0.027 wt. % of a naphthalene sulfonic acid zinc salt rust inhibitor and 0.008 wt. % of a phenolic resin demulsifier. The overbased, sulfurized carboxylate-containing detergent was prepared according to the method described in Example 16 of US Patent Number 5808145 and has a calcium content of 9.3 wt. %, a sulfur content of 2.4 wt. %, a TBN of 260 and a CI of 28.
  • Comparative Example 2
  • An antiwear hydraulic fluid composition was prepared consisting of the baseline formulation above with the addition of 0.075 wt. % of the 56 CI overbased calcium alkyl-substituted hydroxybenzoate as described in Example 1.
  • Comparative Example 3
  • An antiwear hydraulic fluid composition was prepared in accordance with the formulation of Comparative Example 2 except that 0.06 wt. % of the succinate ester dispersant was added.
  • Comparative Example 4
  • An antiwear hydraulic fluid composition was prepared consisting of the baseline formulation above with the addition of 0.15 wt. % of the 56 CI overbased calcium alkylhydroxybenzoate as described in Example 1.
  • Comparative Example 5
  • An antiwear hydraulic fluid composition was prepared in accordance with the formulation of Comparative Example 4 except that 0.06 wt. % of the succinate ester dispersant was added.
  • Results for emulsification performance test
  • The water separability of antiwear hydraulic fluids is characterized in the ASTM D 1401 test method. In this method, a 40 mL volume of the sample material was emulsified with a 40 mL volume of distilled water by stirring the combined liquids in a graduated cylinder at 54°C for 5 minutes. The separation of the emulsion into organic and aqueous layers was characterized by monitoring the relative volumes of the respective fluid, water and emulsion layers after cessation of stirring. Results are set forth below in Table 1 as the respective mL fluid-mL water-mL emulsion observed at minutes after cessation of stirring. Table 1
    Comp. Ex. 1 Comp. Ex. 2 Comp. Ex. 3 Comp. Ex. 4 Comp. Ex. 5 Ex. 1 Ex.2
    56 Cl Ca alkyl-substituted hydroxybenzoate detergent (wt.%) - 0.075 0.075 0.15 0.15 0.225 0.225
    28 Cl Ca alkyl-substituted hydroxybenzoate detergent (wt.%) 0.041 - - - - - -
    CI of antiwear hydraulic fluid composition1 0.01 0.042 0.042 0.084 0.084 0.126 0.126
    Dispersant 0.044 0.044 0.1 0.044 0.1 0.1 0.1
    Zinc dialkyl dithiophosphate 0.31 0.31 0.31 0.31 0.31 0.31 0.47
    Rust inhibitor 0.027 - - - - - -
    Demulsifier 0.008 - - - - - -
    Emulsifier - - - - - - 0.01
    ASTM D 665B (mL fluid-mL water-mL emulsion at minutes after stirring) 40-40-0 44-36-0 40-32-8 42-38-0 0-10-70 0-0-80 0-0-80
    9 min 30 min 40 min 25 min 40 min 40 min 40 min
    40-40-0 46-34-0 40-38-2 43-37-0 0-16-64 0-0-80 0-0-80
    9 min 35 min 40 min 27 min 40 min 40 min 40 min
    1CI of antiwear hydraulic fluid composition = (CI of alkyl-substituted hydroxybenzoate detergent) x (wt. % alkyl-substituted hydroxybenzoate detergent in fluid)
  • Rust Inhibition Performance
  • A base-line formulation was prepared and used for assessing the performance of various detergents in the ASTM D 665 rust prevention test. The base-line formulation contained 0.31 wt. % of a zinc dialkyldithiophosphate, 0.15 wt. % of a hindered phenol antioxidant, 0.044 wt. % of a succinate ester dispersant, 0.044 wt. % of a fatty ester friction modifier, 0.013 wt. % of an arylpolyol demulsifier, 0.008 wt. % of a phenolic resin demulsifier, 0.2 wt. % of a pour point depressant and 0.008 wt. % of a foam inhibitor in a base oil containing ExxonMobil AP/E CORE® basestocks. All finished fluids in these Examples are ISO VG 68.
  • Example 3
  • An antiwear hydraulic fluid composition was prepared consisting of the baseline formulation above with the addition of 0.075 wt. % of the 56 CI overbased calcium alkyl-substituted hydroxybenzoate detergent as described in Example 1.
  • Comparative Example 6
  • An antiwear hydraulic fluid composition was prepared consisting of the baseline formulation above with the addition of 0.041 wt. % of the 28 CI overbased, sulfurized, alkyl-substituted hydroxybenzoate-containing detergent as described in Comparative Example 1, 0.024 wt. % of an overbased calcium phenate and 0.027 wt. % of a naphthalene sulfonic acid zinc salt rust inhibitor.
  • Comparative Example 7
  • An antiwear hydraulic fluid composition was prepared consisting of the baseline formulation above with the addition of 0.067 wt. % of an overbased calcium alkyl-substituted hydroxybenzoate detergent wherein at least 90% of the alkyl groups are C14-C18. The detergent has a TBN of 168 and a CI of 51.
  • Comparative Example 8
  • An antiwear hydraulic fluid composition was prepared consisting of the baseline formulation above with the addition of 0.049 wt. % of an overbased calcium alkyl-substituted hydroxybenzoate detergent wherein at least 90% of the alkyl groups are C20-C28. The detergent has a TBN of 230 and a CI of 46.
  • Comparative Example 9
  • An antiwear hydraulic fluid composition was prepared consisting of the baseline formulation above with the addition of 0.035 wt. % of an overbased calcium alkyl-substituted hydroxybenzoate detergent wherein at least 90% of the alkyl groups are C20-C28. The detergent has a TBN of 325 and a CI of 36.
  • Comparative Example 10
  • An antiwear hydraulic fluid composition was prepared consisting of the baseline formulation above with the addition of 0.032 wt. % of an overbased calcium alkyl-substituted hydroxybenzoate detergent wherein at least 90% of the alkyl groups are C20 or greater. The overbased calcium alkyl-substituted hydroxybenzoate detergent is prepared according to the method described in Example 1 of US Patent Application 2007/0027043 and has a calcium content of 12.5 wt. %, a TBN of 350 and a CI of 37.
  • Results for rust inhibition performance test
  • Rust inhibition of antiwear hydraulic fluids was determined using ASTM D 665. ASTM D 665 is directed at a test for determining the ability of fluid to aid in preventing the rusting of ferrous parts should water become mixed with the fluid. For the determining the rust prevention properties in the instant invention, Procedure B of ASTM D 665 was employed. In this test, a mixture of 300 mL of the test fluid is stirred with 30 mL of synthetic sea water at a temperature of 60°C with a cylindrical steel specimen completely immersed therein for 24 hours. The rust test results are reported as either a "pass" or a "fail." The results are presented in Table 2. Table 2 not according to the invention
    Ex. 3 Comp. Ex. 6 Comp. Ex. 7 Comp. Ex. 8 Comp. Ex. 9 Comp. Ex. 10
    56 Cl alkyl-substituted hydroxybenzoate detergent (wt.%) 0.075 - - - - -
    28 Cl alkyl-substituted hydroxybenzoate (wt.%) - 0.041 - - - -
    51 Cl alkyl-substituted hydroxybenzoate (wt.%) - - 0.067 - - -
    46 Cl alkyl-substituted hydroxybenzoate (wt.%) - - - 0.049 - -
    36 Cl alkyl-substituted hydroxybenzoate (wt.%) - - - - 0.035 -
    37 Cl alkyl-substituted hydroxybenzoate (wt.%) - - - - - 0.032
    Cl of antiwear hydraulic fluid composition1 0.042 0.011 0.034 0.023 0.013 0.012
    Rust Inhibitor (wt. %) - 0.027 - - - -
    Rust Inhibition Result (ASTM D 665B) Pass Pass Fail Fail Fail Fail
    1CI of antiwear hydraulic fluid composition = [CI of alkyl-substituted hydroxybenzoate detergent] x [wt.% alkyl-substituted hydroxybenzoate detergent in fluid]
  • The alkyl-substituted hydroxybenzoate from Example 3 demonstrated unexpected rust inhibiting performance when compared to other carboxylate/salicylate detergents (Comparative Examples 2-5) and also demonstrated unexpected rust inhibiting performance when compared to a formulation containing a rust inhibitor (Comparative Example 6). The formulation of Example 3 advantageously does not require the addition of a rust inhibitor in order to pass this test.
  • As discussed previously, it is advantageous in certain hydraulic fluid applications, such as hydraulic fluids for certain mobile equipment applications and HLPD and HLVPD fluids, to emulsify water, rather than to demulsify water. Since the alkyl-substituted hydroxybenzoate from Example 1 also demonstrated good rust inhibition without the need for a metal sulfonate rust inhibitor and since metal sulfonate rust inhibitors are known to demulsify water, the alkyl-substituted hydroxybenzoate used in Example 1 provides additional performance advantages for such emulsifying hydraulic fluids.

Claims (13)

  1. The use of a composition comprising:
    (a) a major amount of a base oil of lubricating viscosity; and
    (b) a minor amount of at least one oil soluble detergent additive comprising a non-sulfurized calcium salt of an alkyl-substituted hydroxybenzoic acid;
    and further wherein said composition has a Carboxylate Index (as defined herein) of greater than 0.084;
    as an antiwear hydraulic fluid.
  2. The use according to claim 1, wherein said alkyl-substituted hydroxybenzoic acid comprises a linear or branched alkyl group or a mixture of linear and branched alkyl groups.
  3. The use according to claim 1 wherein at least 90% of the alkyl groups of said alkyl-substituted hydroxybenzoic acid are C14 or greater.
  4. The use according to claim 1 wherein said composition is able to achieve an emulsion of 0-0-80 at 40 minutes in the ASTM D 1401 water separability test method.
  5. The use according to claim 1, wherein said composition comprises no added rust inhibitors.
  6. The use according to claim 1, wherein said oil soluble detergent additive comprises a TBN of less than 200 mg KOH/g.
  7. The use according to claim 1, wherein said oil soluble detergent additive comprises a TBN of less than 160 mg KOH/g.
  8. The use according to claim 1, wherein said oil soluble detergent additive comprises greater than 0.1 weight percent of the total weight of said composition.
  9. The use according to claim 1, wherein said oil soluble detergent additive comprises greater than 0.2 weight percent of the total weight of said composition.
  10. The use according to claim 1, wherein the composition further comprises at least one of these co-additives: (a) an ashless dispersant; (b) an oxidation inhibitor; (d) a demulsifier; (e) an extreme pressure agent; (f) a friction modifier; (g) a multifunctional additive; (h) a viscosity index improver; (i) a pour point depressant; (j) a foam inhibitor; and (k) an emulsifier.
  11. The use according to claim 1 wherein said composition is able to achieve a pass result in the ASTM D 665 rust inhibition method.
  12. The use according to claim 1, wherein said oil soluble detergent additive comprises greater than 0.05 weight percent of the total weight of said composition.
  13. The use according to claim 1, wherein said oil soluble detergent additive comprises greater than 0.07 weight percent of the total weight of said composition.
EP09803603.1A 2008-07-31 2009-07-30 Use as an antiwear hydraulic fluid composition Active EP2307532B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP13180664.8A EP2669355A1 (en) 2008-07-31 2009-07-30 Antiwear hydraulic fluid composition with useful emulsifying and rust prevention properties

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US12/184,094 US20100029525A1 (en) 2008-07-31 2008-07-31 Antiwear hydraulic fluid composition with useful emulsifying and rust prevention properties
PCT/US2009/052286 WO2010014833A2 (en) 2008-07-31 2009-07-30 Antiwear hydraulic fluid composition with useful emulsifying and rust prevention properties

Publications (3)

Publication Number Publication Date
EP2307532A2 EP2307532A2 (en) 2011-04-13
EP2307532A4 EP2307532A4 (en) 2012-02-15
EP2307532B1 true EP2307532B1 (en) 2013-08-21

Family

ID=41608974

Family Applications (2)

Application Number Title Priority Date Filing Date
EP09803603.1A Active EP2307532B1 (en) 2008-07-31 2009-07-30 Use as an antiwear hydraulic fluid composition
EP13180664.8A Withdrawn EP2669355A1 (en) 2008-07-31 2009-07-30 Antiwear hydraulic fluid composition with useful emulsifying and rust prevention properties

Family Applications After (1)

Application Number Title Priority Date Filing Date
EP13180664.8A Withdrawn EP2669355A1 (en) 2008-07-31 2009-07-30 Antiwear hydraulic fluid composition with useful emulsifying and rust prevention properties

Country Status (7)

Country Link
US (1) US20100029525A1 (en)
EP (2) EP2307532B1 (en)
JP (2) JP5945414B2 (en)
CN (1) CN102105571B (en)
CA (1) CA2730058A1 (en)
SG (2) SG10201700780WA (en)
WO (1) WO2010014833A2 (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101261880B1 (en) 2012-11-29 2013-05-08 (주)이바이오텍 A high-funcitional engine oil additives of multipurpose internal combustion engine and method of manufacturing
WO2019003178A1 (en) * 2017-06-30 2019-01-03 Chevron Oronite Company Llc Lubricating oil compositions containing detergent compounds
EP3645679B1 (en) * 2017-06-30 2022-08-03 Chevron Oronite Company LLC Lubricating oil magnesium detergents and method of making and using same
CN109370736B (en) * 2018-11-29 2021-02-09 郑州正赢石化有限公司 Alkali-resistant ashless hydraulic oil
CN110484332B (en) * 2019-09-16 2021-08-31 辽宁百特润滑科技有限责任公司 Hydraulic oil composite additive, preparation method thereof and hydraulic oil
CN114075473B (en) * 2020-08-18 2022-12-13 中国石油化工股份有限公司 Emulsified hydraulic oil composition

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH05311187A (en) * 1992-05-01 1993-11-22 Idemitsu Kosan Co Ltd Heat-resistant hydraulic oil composition

Family Cites Families (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5691283A (en) * 1994-03-01 1997-11-25 Ethyl Petroleum Additives Limited Use of transmission and gear oil lubricants having enhanced friction properties
FR2717491B1 (en) 1994-03-17 1996-06-07 Chevron Chem Sa Detergent-dispersant additives for lubricating oils of the alkylsalicylates-alkylphenates, alkaline-earth, sulphurized and over-alkalized type.
JPH07258675A (en) * 1994-03-28 1995-10-09 Cosmo Sogo Kenkyusho:Kk Hydraulic pressure oil composition for buffer
FR2731427B1 (en) * 1995-03-08 1997-05-30 Chevron Chem Sa ISOMERIZED LINEAR ALKYLARYL-SULFONATES USEFUL AS ADDITIVES FOR LUBRICATING OILS AND CORRESPONDING ALKYLARYL HYDOCARBONS
EP0933417B1 (en) * 1998-01-30 2003-04-02 Chevron Chemical S.A. Unsulfurized, alkali metal-free, additive for lubricating oils
DE19813999C1 (en) 1998-03-28 1999-11-25 Seepex Seeberger Gmbh & Co Eccentric screw pump
JPH11302679A (en) * 1998-04-24 1999-11-02 Japan Energy Corp Lubricating oil composition
FR2783824B1 (en) * 1998-09-25 2001-01-05 Chevron Chem Sa LOW-BASED ALKYLARYL SULFONATES AND LUBRICATING OIL CONTAINING THEM
JP3927724B2 (en) * 1999-04-01 2007-06-13 東燃ゼネラル石油株式会社 Lubricating oil composition for internal combustion engines
CN1229477C (en) 1999-04-14 2005-11-30 国际壳牌研究有限公司 Hydraulic fluid
US6569818B2 (en) * 2000-06-02 2003-05-27 Chevron Oronite Company, Llc Lubricating oil composition
EP1233052A1 (en) * 2001-02-16 2002-08-21 Infineum International Limited Overbased detergent additives
US7163911B2 (en) * 2003-05-22 2007-01-16 Chevron Oronite Company Llc Carboxylated detergent-dispersant additive for lubricating oils
US8618029B2 (en) * 2003-12-22 2013-12-31 Chevron Oronite S.A. Overbased detergents for lubricating oil applications
US8188020B2 (en) * 2003-12-22 2012-05-29 Chevron Oronite S.A. Lubricating oil composition containing an alkali metal detergent
US7585822B2 (en) * 2004-11-23 2009-09-08 Crompton Corporation Emulsifier blends for lubricating oils
US7662271B2 (en) * 2005-12-21 2010-02-16 Chevron U.S.A. Inc. Lubricating oil with high oxidation stability
US8030258B2 (en) * 2005-07-29 2011-10-04 Chevron Oronite Company Llc Overbased alkaline earth metal alkylhydroxybenzoates having low crude sediment

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH05311187A (en) * 1992-05-01 1993-11-22 Idemitsu Kosan Co Ltd Heat-resistant hydraulic oil composition

Also Published As

Publication number Publication date
CN102105571A (en) 2011-06-22
JP5945414B2 (en) 2016-07-05
EP2307532A4 (en) 2012-02-15
US20100029525A1 (en) 2010-02-04
EP2669355A1 (en) 2013-12-04
EP2307532A2 (en) 2011-04-13
CA2730058A1 (en) 2010-02-04
SG193167A1 (en) 2013-09-30
WO2010014833A3 (en) 2010-05-06
WO2010014833A2 (en) 2010-02-04
JP2015091982A (en) 2015-05-14
JP2011529994A (en) 2011-12-15
CN102105571B (en) 2014-01-29
SG10201700780WA (en) 2017-03-30

Similar Documents

Publication Publication Date Title
EP2308953B1 (en) System oil formulation for marine two-stroke engines containing alkyl salicylates
CA2467640C (en) Unsulfurized, carboxylate-containing additive for lubrication oils
EP2295527B1 (en) An anti-wear additive composition and lubricating oil composition comprising the same
EP1059301B1 (en) Alkaline earth alkylaryl sulfonates, their application as an additive for lubricating oil, and methods of preparation
EP2307532B1 (en) Use as an antiwear hydraulic fluid composition
EP1548089A1 (en) Lubricating oil composition containing an alkali metal salicylate detergent
KR102260148B1 (en) Tractor hydraulic fluid compositions
US20120165235A1 (en) Glycerol-containing functional fluid
CA2852488A1 (en) Diesel engine oils
EP2776542B1 (en) Glycerol-containing functional fluid
JP2014533313A (en) Glycerol-containing functional liquid
CA2756951C (en) Lubricating oil compositions comprising polycyclic imides

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20110221

AK Designated contracting states

Kind code of ref document: A2

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO SE SI SK SM TR

AX Request for extension of the european patent

Extension state: AL BA RS

DAX Request for extension of the european patent (deleted)
A4 Supplementary search report drawn up and despatched

Effective date: 20120117

RIC1 Information provided on ipc code assigned before grant

Ipc: C10N 30/04 20060101ALI20120111BHEP

Ipc: C10N 30/12 20060101ALI20120111BHEP

Ipc: C10M 129/04 20060101AFI20120111BHEP

Ipc: C10M 159/22 20060101ALI20120111BHEP

Ipc: C10M 135/02 20060101ALI20120111BHEP

Ipc: C10M 125/10 20060101ALI20120111BHEP

17Q First examination report despatched

Effective date: 20120926

REG Reference to a national code

Ref country code: DE

Ref legal event code: R079

Ref document number: 602009018264

Country of ref document: DE

Free format text: PREVIOUS MAIN CLASS: C10M0129040000

Ipc: C10N0030040000

RIC1 Information provided on ipc code assigned before grant

Ipc: C10N 30/04 20060101AFI20130206BHEP

Ipc: C10N 30/12 20060101ALI20130206BHEP

Ipc: C10M 159/22 20060101ALI20130206BHEP

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

INTG Intention to grant announced

Effective date: 20130416

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO SE SI SK SM TR

REG Reference to a national code

Ref country code: GB

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

REG Reference to a national code

Ref country code: AT

Ref legal event code: REF

Ref document number: 628117

Country of ref document: AT

Kind code of ref document: T

Effective date: 20130915

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: DE

Ref legal event code: R096

Ref document number: 602009018264

Country of ref document: DE

Effective date: 20131017

REG Reference to a national code

Ref country code: NL

Ref legal event code: T3

REG Reference to a national code

Ref country code: AT

Ref legal event code: MK05

Ref document number: 628117

Country of ref document: AT

Kind code of ref document: T

Effective date: 20130821

REG Reference to a national code

Ref country code: LT

Ref legal event code: MG4D

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: AT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20130821

Ref country code: NO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20131121

Ref country code: SE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20130821

Ref country code: CY

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20130717

Ref country code: LT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20130821

Ref country code: IS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20131221

Ref country code: HR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20130821

Ref country code: PT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20131223

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20131122

Ref country code: SI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20130821

Ref country code: BE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20130821

Ref country code: PL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20130821

Ref country code: LV

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20130821

Ref country code: FI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20130821

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: CY

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20130821

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: EE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20130821

Ref country code: DK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20130821

Ref country code: RO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20130821

Ref country code: SK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20130821

Ref country code: CZ

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20130821

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: ES

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20130821

Ref country code: IT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20130821

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

26N No opposition filed

Effective date: 20140522

REG Reference to a national code

Ref country code: DE

Ref legal event code: R097

Ref document number: 602009018264

Country of ref document: DE

Effective date: 20140522

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LU

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140730

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

REG Reference to a national code

Ref country code: IE

Ref legal event code: MM4A

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: CH

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20140731

Ref country code: LI

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20140731

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20140730

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SM

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20130821

Ref country code: MC

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20130821

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 8

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: BG

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20130821

Ref country code: MT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20130821

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: HU

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT; INVALID AB INITIO

Effective date: 20090730

Ref country code: TR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20130821

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 9

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 10

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20130821

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: NL

Payment date: 20200715

Year of fee payment: 12

REG Reference to a national code

Ref country code: DE

Ref legal event code: R082

Ref document number: 602009018264

Country of ref document: DE

Representative=s name: HL KEMPNER PATENTANWAELTE, SOLICITORS (ENGLAND, DE

Ref country code: DE

Ref legal event code: R082

Ref document number: 602009018264

Country of ref document: DE

Representative=s name: HL KEMPNER PATENTANWALT, RECHTSANWALT, SOLICIT, DE

REG Reference to a national code

Ref country code: NL

Ref legal event code: MM

Effective date: 20210801

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20210801

P01 Opt-out of the competence of the unified patent court (upc) registered

Effective date: 20230530

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 20230620

Year of fee payment: 15

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20230608

Year of fee payment: 15

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20230607

Year of fee payment: 15