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US20070191237A1 - Hydraulic fluid - Google Patents

Hydraulic fluid Download PDF

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Publication number
US20070191237A1
US20070191237A1 US11/691,198 US69119807A US2007191237A1 US 20070191237 A1 US20070191237 A1 US 20070191237A1 US 69119807 A US69119807 A US 69119807A US 2007191237 A1 US2007191237 A1 US 2007191237A1
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Prior art keywords
magnesium
salicylate
hydraulic fluid
weight loss
amount
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US11/691,198
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Andrew Holmes
Cameron Watson
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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
    • C10M163/00Lubricating compositions characterised by the additive being a mixture of a compound of unknown or incompletely defined constitution and a non-macromolecular compound, each of these compounds being essential
    • 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
    • C10M2207/26Overbased 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
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/04Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • 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
    • C10N2010/00Metal present as such or in compounds
    • C10N2010/04Groups 2 or 12
    • 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
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/08Hydraulic fluids, e.g. brake-fluids

Definitions

  • the present invention relates to a hydraulic fluid.
  • WO 93/03121 relates to hydraulic fluids having improved wet filterability and having increased resistance to loss of zinc when the oil is exposed to water.
  • These compositions comprise (A) a combination of a metal salt selected from the group consisting of sulfonates, phenates, carboxylates and mixtures thereof, (B) an aliphatic carboxylic acid or anhydride, or carboxylic acid group containing derivative thereof, wherein the aliphatic group contains at least 20 carbon atoms, and optionally (C) a metal salt of (C)(I) at least one organic phosphorus acid or mixture of (C)(I) at least one organic phosphorus acid and (C)(II) at least one carboxylic acid group, and optionally (D) triazole.
  • a metal salt selected from the group consisting of sulfonates, phenates, carboxylates and mixtures thereof
  • B an aliphatic carboxylic acid or anhydride, or carboxylic acid group containing derivative thereof, where
  • the carboxylic acids of (A) are aromatic carboxylic acids.
  • Zinc, calcium and magnesium salts of these aromatic carboxylic acids, and especially salicylic acids, are preferred.
  • magnesium salicylate and zinc dithiophosphate are both mentioned per se, there is no teaching to use the combination of these compounds.
  • WO 89/04358 relates to compositions comprising (A) a neutral or basic metal salt of an acidic organic compound, (B) a metal deactivator, preferably an optionally substituted benzotriazole, and (C) a sulfur and/or phosphorus-containing compound selected from the group consisting of (C-1) phosphorus-containing amide, (C-2) phosphorus-containing ester, (C-3) sulfur-coupled dithiocarbamate, (C-4) sulfur-containing compound according to formula (I).
  • Particularly preferred metals for the salts (A) are sodium, magnesium, calcium or mixtures of two or more thereof.
  • zinc dialkyl dithiophosphate is mentioned. Although magnesium salicylate and zinc dithiophosphate are both mentioned per se, there is no teaching to use the combination of these compounds.
  • EP-A-604 218 describes functional fluids comprising a major amount of an oil of lubricating viscosity, at least one metal salt of thiophosphoric acid, a zinc salt of salicylic acid, and a rust inhibitor, which fluid contains less than about 1% wt of dispersant and less than about 1% wt of basic sulfonate salt.
  • the thiophosphoric acid is most commonly a dihydrocarbyl dithiophosphoric acid; the metal is most preferably zinc.
  • the teaching of the document is restricted to the use of zinc salicylate.
  • Hydraulic fluids need to meet special requirements as they both lubricate and transmit pressure.
  • hydraulic fluids contain additives.
  • hydraulic fluids contain antiwear/extreme pressure additives.
  • the conditions for a hydraulic fluid are especially difficult in vane pumps where the vane tips slide against the casing at high speed under heavy load and at high temperature.
  • the increasingly high operating temperatures of modern hydraulic equipment requires the fluid to be thermally stable to avoid the formation of deposits and sludge and to resist the corrosion of both ferrous and non-ferrous metals.
  • the requirement of good thermal stability in hydraulic fluids containing an anti-wear additive means that these additives are often used in combination with detergents.
  • the calcium salts of alkylbenzene sulphonates, alkyl-naphthalene sulphonates, petroleum sulphonates, alkylphenates, alkyl sulphurized phenates or alkylsalicylates which are usually applied, give increased wear.
  • the increased wear is especially marked in vane pumps, more specifically under low load conditions. Low load conditions occur in practice when the pump is idle.
  • hydraulic fluid containing a combination of magnesium salicylate and zinc dithiophosphate gives improved performance at low load compared with a combination containing calcium salicylate. Additionally, it was found that this combination also provides greater thermal stability. Less sludge and deposits are formed when subjecting the hydraulic fluid of the present invention to the Cincinnati Milacron Thermal Stability Test.
  • the present invention provides a hydraulic fluid comprising a lubricant base oil in combination with (a) from 0.001 to 5% wt of magnesium salicylate, (b) from 0.01 to 8% wt of zinc dithiophosphate, which amounts are based on total weight of hydraulic fluid.
  • the magnesium salicylate for use in the present invention can be either neutral or overbased.
  • the expression “overbased” is equivalent to “basic”, “superbased”, “hyperbased” and “high-metal containing salts”. These magnesium salicylates contain an excess metal content compared to the amount of metal which would be present according to the stoichiometry of the metal and the salicylic acid reacted with the metal.
  • Processes for making such neutral and basic metal salts are well known in the art.
  • Neutral salts can be made by heating a mineral oil solution of an acidic organic compound with a stoichiometric equivalent amount of a metal neutralizing agent such as the metal oxide, hydroxide, carbonate, bicarbonate, or sulfide at a temperature above 50° C. and filtering the resulting mass.
  • Basic salts are made similarly with the exception that a stoichiometric excess of the metal is used.
  • overbased magnesium salicylate is used.
  • These compositions can be characterized by their total base number (TBN).
  • TBN total base number
  • the total base number is preferably at least 100 mg KOH/g, more preferably at least 200 mg KOH/g, most preferably at least 300 mg KOH/g.
  • the total base number is preferably at most 600 mg KOH/g.
  • Another method of characterising overbased magnesium salicylates is by the magnesium content relative to the stoichiometrically equivalent amount of magnesium based on the amount of total acid present.
  • Overbased magnesium salicyclates for use in the present invention preferably have a magnesium content of more than 500% of the stoichiometrically equivalent amount of magnesium based on the amount of total acid present, more preferably at least 550%.
  • the salicylate can be either substituted or unsubstituted. Suitable substituents include aliphatic groups containing from 1 to 40 carbon atoms and optionally containing one or more oxygen and/or nitrogen atoms, and hydroxy groups. Preferred substituents are alkyl groups containing from 6 to 30 carbon atoms, preferably from 12 to 20 carbon atoms. Preferably, the substituents are linear.
  • the salicylate can contain from 1 to 4 substituents, preferably from 1 to 3, most preferably 1 or 2 substituents. Most preferably, the salicylate is substituted by 1 linear alkyl group containing from 14 to 18 carbon atoms.
  • mono-alkyl salycylic acids are prepared by alkylation of phenol and subsequent carboxylation. Therefore, a small amount (generally at most 20% mol) of dialkyl salicylate and unsubstituted salicylate can be present in the mono-alkyl salicylate.
  • Magnesium salicylate which can be used in the present invention, is commercially available.
  • a suitable commercial product is SAP 007 (ex Infineum).
  • SAP 007 Ex Infineum
  • the magnesium salicylate will usually be supplied in combination with mineral oil.
  • the amounts referred to in this document, relate to the compound per se without mineral oil.
  • Zinc dithiophosphate is well known in the art.
  • Preferred dithiophosphate for use in the present invention are represented by the following formula in which R8 and R9 can be either hydrogen or an aliphatic group.
  • the aliphatic group is preferably a hydrocarbyl group.
  • the hydrocarbyl group optionally contains an acid, a hydroxy and/or an ester group.
  • the hydrocarbyl group is preferably an alkyl containing up to 12 carbon atoms optionally further containing an acid, a hydroxy and/or an ester group.
  • the hydrocarbyl substituted dithiophosphate can contain 1 or 2 aliphatic groups, or it can be a mixture of dithiophosphates having 1 aliphatic group and dithiophosphates having 2 aliphatic groups.
  • the zinc dithiophosphate is a zinc dialkyl dithiophosphate.
  • Substituted dithiophosphates can contain primary, secondary and/or tertiary aliphatic substituents, i.e. substituents which are attached to the oxygen atom via a carbon atom attached to one, two or three further carbon atoms, respectively.
  • primary aliphatic substituents i.e. substituents which are attached to the oxygen atom via a carbon atom attached to one, two or three further carbon atoms, respectively.
  • Suitable zinc dithiophosphates which are commercially available include Elco 108 (ex Elco Corporation), Lz 1375 (ex Lubrizol), OLOA 4269Q (ex Oronite) and HITEC 680 (ex Ethyl).
  • the amount of magnesium salicylate which is present is preferably at most 1% wt, based on total composition, more preferably at most 0.5% wt, most preferably at most 0.3% wt.
  • the amount of magnesium salicylate which is present is preferably at least 0.001% wt, more preferably at least 0.005 % wt more preferably at least 0.01% wt, most preferably at least 0.015% wt.
  • the amount of zinc dithiophosphate which is present is preferably at most 5% wt, based on total composition, more preferably at most 3% wt, most preferably at most 1% wt.
  • the amount of zinc dithiophosphate which is present is preferably at least 0.05% wt, more preferably at least 0.7% wt, most preferably at least 0.1% wt.
  • the hydraulic fluid can further comprise (c) from 0.001 to 5% wt of a rust inhibitor based on total composition, preferably a carboxylic acid or ester or amide or imide containing compound, more preferably a dicarboxylic acid or its mono- or di-ester or its mono-amide or di-amide or imide, more preferably a dicarboxylic acid or its ester, amide or imide containing a total number of between 4 and 70 carbon atoms. More preferably, the number of carbon atoms of the compound is between 20 and 40.
  • a preferred compound is an aliphatic succinimide or succinic diamide. Such compounds have been described in EP-A-776964.
  • (c) is from 0.001 to 5% wt of a compound according to the following formula I in which R 1 and R 2 are each hydrogen or alkyl or hydroxyalkyl of 1 to 30 carbon atoms; R 3 , R 4 and R 5 are each hydrogen or alkyl or hydroxyalkyl of 1 to 4 carbon atoms; X is CH or N and R 6 and R 7 are each hydrogen, alkyl or alkenyl of 1 to 30 carbon atoms, or an acyl group derived from a saturated or unsaturated carboxylic acid of up to 30 carbon atoms.
  • R 1 and R 2 are each an alkyl of from 3 to 6 carbon atoms
  • R 3 , R 4 and R 5 are each hydrogen
  • X is N
  • R 6 and R 7 are each an alkyl of 15 to 20 carbon atoms or an acyl group derived from a saturated or unsaturated dicarboxylic acid containing 4 to 10 carbon atoms, at least one of R 6 and R 7 being an acyl group.
  • aspartic acid N-(3-carboxy-1-oxo-2-propenyl)-octadecyl-bis(2-methylpropyl)ester.
  • Such aspartic acid esters are commercially available. Processes for preparing such compounds having been described in EP-A-434 464.
  • the hydraulic fluid comprises magnesium salicylate, zinc dithiophosphate and optionally a rust inhibitor in such quantities that the weight ratio of magnesium salicylate to zinc dithiophosphate is from 1:5 to 1:100 and the weight ratio of magnesium salicylate to rust inhibitor is from 1:0 to 1:50.
  • the lubricant base oils present in the hydraulic fluid of the present invention can be any base fluid which is suitable for use in hydraulic fluids.
  • the base oil can be a natural or a synthetic lubricant base oil, or a mixture thereof.
  • the natural oil can be an animal oil or vegetable oil, such as lard oil or castor oil, or a mineral oil such as liquid petroleum oils and solvent treated or acid treated mineral lubricating oil of the paraffinic, naphthenic, or mixed paraffinic/naphthenic type which may be further refined by hydrocracking and hydrofinishing processes and/or dewaxing.
  • Synthetic lubricating oils include hydrocarbon oils and halo-substituted hydrocarbon oils such as polymerised and interpolymerised olefins.
  • a suitable base oil contains poly-alpha-olefins, such as polydecene.
  • the base oil is a hydrocarbon base oil.
  • the base fluid is a mineral oil which contains less than 10% by weight of aromatic compounds, preferably less than 5% by weight, most preferably less than 3.0% by weight, measured according to DIN 51378. It is further preferred that the base oil contains less than 1.0% wt of sulphur, calculated as elemental sulphur, preferably less than 0.1% wt, more preferably less than 0.05% wt, measured according to ASTM D 4045.
  • Such mineral oils can be prepared by severe hydroprocessing.
  • the lubricating oil has a kinematic viscosity in the range of from 5 to 220 cSt at 40° C., more preferably of from 10 to 200 cSt, most preferably of from 20 to 100 cSt.
  • the hydraulic fluid according to the present invention can contain further additives usually present in hydraulic fluids, such as pour point depressants, anti-foam agents and demulsifier.
  • Pour point depressants generally are high molecular weight polymers such as alkylaromatic polymers and polymethacrylates.
  • anti-foam agents silicone polymers and/or polymethacrylates are generally used.
  • Demulsifiers which are generally applied are polyalkylene glycol ethers.
  • detergents such as sulphonates and phenates, metal deactivators, antioxidants such as phenolic compounds, diphenyl amines and phenyl naphthyl amines, ashless anti-wear agents and/or ashless dispersants, such as succinimides, can be present.
  • the hydraulic fluids of the present invention contain magnesium salicylate.
  • the fluids contain a combination of magnesium and calcium salicylate.
  • the components of the present invention can be added per se to a lubricating oil, or they can be mixed into an additive package before being added to the lubricating oil.
  • the additive package for preparing the hydraulic fluid preferably contains magnesium salicylate, zinc dithiophosphate and optionally a dicarboxylic acid or its mono- or di-ester or its mono-amide or di-amide or imide containing in total between 4 and 70 carbon atoms, wherein the weight ratio of magnesium salicylate to zinc dithiophosphate is from 1:5 to 1:100 and the weight ratio of magnesium salicylate to dicarboxylic acid or its mono- or di-ester or its mono-amide or di-amide or imide is from 1:0 to 1:50.
  • Magnesium salicylate highly overbased magnesium alkylsalicylate having a total base number of 337 mg KOH/g (SAP 007 ex INFINEUM) and a magnesium content of about 750% of the stoichiometrically equivalent amount of magnesium based on the amount of total acid, containing 40% wt of mineral oil
  • Calcium salicylate overbased calcium alkylsalicylate having a total base number of 168 mg KOH/g (SAP 001 ex INFINEUM), containing 40% wt of mineral oil.
  • the amounts of metal salicylate mentioned in Table 1, are the amounts of metal salicylate per se, without mineral oil.
  • Zinc dithiophosphate zinc di(ethyl-hexyl)dithiophosphate (Elco 108 ex Elco corporation)
  • compositions obtained are described in Table 1.
  • the amounts are of the compounds per se, excluding the mineral oil.
  • Compositions 1 and 2 were used in Vickers V104C vane pump tests. A new pump cartridge was used for each test. The test duration was 250 hours, performed at a fluid temperature of about 66° C., at a fluid outlet pressure of 35 bar (3.5 MPa) and at a pump speed of 1450 revolutions per minute. The results are described in Table 1.
  • Composition 1 magnesium salicylate 0.06% wt — calcium salicylate — 0.06% wt zinc dithiophosphate 0.37% wt 0.37% wt compound of formula I 0.10% wt 0.10% wt lubricant base oil balance balance Low load test ring weight loss (mg) 13 96 vane weight loss (mg) 2 1 total weight loss (mg) 15 97

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

Abstract

A method for reducing total wear-induced weight loss during wear-inducing operation of equipment, the method comprises a) providing a hydraulic fluid comprising a combination of an amount of zinc dithiophosphate and a quantity of magnesium salicylate, wherein said quantity of magnesium salicylate is from 0.001 to at most 1% wt and said amount of zinc dithiophosphate is from 0.01 to 1% wt. and b) operating the equipment using the hydraulic fluid under wear-inducing conditions that reduce the weight of the equipment. The hydraulic fluid is effective to produce a first total weight loss that is less than a second total weight loss that would be observed using a second hydraulic fluid comprising a quantity of calcium salicylate in place of said quantity of magnesium salicylate.

Description

    RELATED CASES
  • The present application is a divisional of U.S. application Ser. No. 09/648,325, filed Aug. 25, 2000, which is incorporated herein by reference.
  • FIELD OF THE INVENTION
  • The present invention relates to a hydraulic fluid.
  • BACKGROUND OF THE INVENTION
  • WO 93/03121 relates to hydraulic fluids having improved wet filterability and having increased resistance to loss of zinc when the oil is exposed to water. These compositions comprise (A) a combination of a metal salt selected from the group consisting of sulfonates, phenates, carboxylates and mixtures thereof, (B) an aliphatic carboxylic acid or anhydride, or carboxylic acid group containing derivative thereof, wherein the aliphatic group contains at least 20 carbon atoms, and optionally (C) a metal salt of (C)(I) at least one organic phosphorus acid or mixture of (C)(I) at least one organic phosphorus acid and (C)(II) at least one carboxylic acid group, and optionally (D) triazole. In one embodiment, the carboxylic acids of (A) are aromatic carboxylic acids. Zinc, calcium and magnesium salts of these aromatic carboxylic acids, and especially salicylic acids, are preferred. Although magnesium salicylate and zinc dithiophosphate are both mentioned per se, there is no teaching to use the combination of these compounds.
  • WO 89/04358 relates to compositions comprising (A) a neutral or basic metal salt of an acidic organic compound, (B) a metal deactivator, preferably an optionally substituted benzotriazole, and (C) a sulfur and/or phosphorus-containing compound selected from the group consisting of (C-1) phosphorus-containing amide, (C-2) phosphorus-containing ester, (C-3) sulfur-coupled dithiocarbamate, (C-4) sulfur-containing compound according to formula (I). Particularly preferred metals for the salts (A) are sodium, magnesium, calcium or mixtures of two or more thereof. In the extensive list of additional compounds which can be present, zinc dialkyl dithiophosphate is mentioned. Although magnesium salicylate and zinc dithiophosphate are both mentioned per se, there is no teaching to use the combination of these compounds.
  • EP-A-604 218 describes functional fluids comprising a major amount of an oil of lubricating viscosity, at least one metal salt of thiophosphoric acid, a zinc salt of salicylic acid, and a rust inhibitor, which fluid contains less than about 1% wt of dispersant and less than about 1% wt of basic sulfonate salt. The thiophosphoric acid is most commonly a dihydrocarbyl dithiophosphoric acid; the metal is most preferably zinc. The teaching of the document is restricted to the use of zinc salicylate.
  • In U.S. Pat. No. 4,627,928, a process has been described for preparing basic magnesium salicylates which can be characterised as having a magnesium content of at least 150% up to 500%, of the stoichiometrically equivalent amount of magnesium based on the amount of total acid present. The magnesium salts obtained are described to be suitable for use as additives in general, more specifically as additives for a variety of lubricating oils and fuels, e.g. gasoline and diesel fuels. It is mentioned that these specific magnesium salicylates can be used in combination with a wide range of other compounds. There is no disclosure or teaching to apply a combination of zinc dithiophosphate and magnesium salicylate in a hydraulic fluid.
  • Hydraulic fluids need to meet special requirements as they both lubricate and transmit pressure. In order to meet these requirements, hydraulic fluids contain additives. Generally, hydraulic fluids contain antiwear/extreme pressure additives. The conditions for a hydraulic fluid are especially difficult in vane pumps where the vane tips slide against the casing at high speed under heavy load and at high temperature. Further, the increasingly high operating temperatures of modern hydraulic equipment requires the fluid to be thermally stable to avoid the formation of deposits and sludge and to resist the corrosion of both ferrous and non-ferrous metals. The requirement of good thermal stability in hydraulic fluids containing an anti-wear additive, means that these additives are often used in combination with detergents. However, the calcium salts of alkylbenzene sulphonates, alkyl-naphthalene sulphonates, petroleum sulphonates, alkylphenates, alkyl sulphurized phenates or alkylsalicylates which are usually applied, give increased wear. The increased wear is especially marked in vane pumps, more specifically under low load conditions. Low load conditions occur in practice when the pump is idle.
  • SUMMARY OF THE INVENTION
  • It has now surprisingly been found that hydraulic fluid containing a combination of magnesium salicylate and zinc dithiophosphate, gives improved performance at low load compared with a combination containing calcium salicylate. Additionally, it was found that this combination also provides greater thermal stability. Less sludge and deposits are formed when subjecting the hydraulic fluid of the present invention to the Cincinnati Milacron Thermal Stability Test.
  • The present invention provides a hydraulic fluid comprising a lubricant base oil in combination with (a) from 0.001 to 5% wt of magnesium salicylate, (b) from 0.01 to 8% wt of zinc dithiophosphate, which amounts are based on total weight of hydraulic fluid.
  • DETAILED DESCRIPTION OF THE INVENTION
  • The magnesium salicylate for use in the present invention can be either neutral or overbased. The expression “overbased” is equivalent to “basic”, “superbased”, “hyperbased” and “high-metal containing salts”. These magnesium salicylates contain an excess metal content compared to the amount of metal which would be present according to the stoichiometry of the metal and the salicylic acid reacted with the metal. Processes for making such neutral and basic metal salts are well known in the art. Neutral salts can be made by heating a mineral oil solution of an acidic organic compound with a stoichiometric equivalent amount of a metal neutralizing agent such as the metal oxide, hydroxide, carbonate, bicarbonate, or sulfide at a temperature above 50° C. and filtering the resulting mass. Basic salts are made similarly with the exception that a stoichiometric excess of the metal is used.
  • Preferably, overbased magnesium salicylate is used. These compositions can be characterized by their total base number (TBN). The total base number is preferably at least 100 mg KOH/g, more preferably at least 200 mg KOH/g, most preferably at least 300 mg KOH/g. The total base number is preferably at most 600 mg KOH/g. Another method of characterising overbased magnesium salicylates is by the magnesium content relative to the stoichiometrically equivalent amount of magnesium based on the amount of total acid present. Overbased magnesium salicyclates for use in the present invention preferably have a magnesium content of more than 500% of the stoichiometrically equivalent amount of magnesium based on the amount of total acid present, more preferably at least 550%.
  • The salicylate can be either substituted or unsubstituted. Suitable substituents include aliphatic groups containing from 1 to 40 carbon atoms and optionally containing one or more oxygen and/or nitrogen atoms, and hydroxy groups. Preferred substituents are alkyl groups containing from 6 to 30 carbon atoms, preferably from 12 to 20 carbon atoms. Preferably, the substituents are linear. The salicylate can contain from 1 to 4 substituents, preferably from 1 to 3, most preferably 1 or 2 substituents. Most preferably, the salicylate is substituted by 1 linear alkyl group containing from 14 to 18 carbon atoms.
  • Generally, mono-alkyl salycylic acids are prepared by alkylation of phenol and subsequent carboxylation. Therefore, a small amount (generally at most 20% mol) of dialkyl salicylate and unsubstituted salicylate can be present in the mono-alkyl salicylate.
  • Magnesium salicylate which can be used in the present invention, is commercially available. A suitable commercial product is SAP 007 (ex Infineum). The magnesium salicylate will usually be supplied in combination with mineral oil. The amounts referred to in this document, relate to the compound per se without mineral oil.
  • A process by which suitable magnesium salicylate can be prepared, has been described in U.S. Pat. No. 4,627,928.
  • Zinc dithiophosphate is well known in the art. Preferred dithiophosphate for use in the present invention are represented by the following formula
    Figure US20070191237A1-20070816-C00001

    in which R8 and R9 can be either hydrogen or an aliphatic group. The aliphatic group is preferably a hydrocarbyl group. The hydrocarbyl group optionally contains an acid, a hydroxy and/or an ester group. The hydrocarbyl group is preferably an alkyl containing up to 12 carbon atoms optionally further containing an acid, a hydroxy and/or an ester group. The hydrocarbyl substituted dithiophosphate can contain 1 or 2 aliphatic groups, or it can be a mixture of dithiophosphates having 1 aliphatic group and dithiophosphates having 2 aliphatic groups. Preferably, the zinc dithiophosphate is a zinc dialkyl dithiophosphate.
  • Substituted dithiophosphates can contain primary, secondary and/or tertiary aliphatic substituents, i.e. substituents which are attached to the oxygen atom via a carbon atom attached to one, two or three further carbon atoms, respectively. In the present invention, it is preferred that at least 60% wt of the aliphatic, preferably alkyl, substituents of the zinc dithiophosphate, are primary aliphatic substituents. More preferably at least 80% wt of the aliphatic substituents are primary aliphatic substituents.
  • Suitable zinc dithiophosphates which are commercially available include Elco 108 (ex Elco Corporation), Lz 1375 (ex Lubrizol), OLOA 4269Q (ex Oronite) and HITEC 680 (ex Ethyl).
  • The amount of magnesium salicylate which is present is preferably at most 1% wt, based on total composition, more preferably at most 0.5% wt, most preferably at most 0.3% wt. The amount of magnesium salicylate which is present is preferably at least 0.001% wt, more preferably at least 0.005 % wt more preferably at least 0.01% wt, most preferably at least 0.015% wt. The amount of zinc dithiophosphate which is present is preferably at most 5% wt, based on total composition, more preferably at most 3% wt, most preferably at most 1% wt. The amount of zinc dithiophosphate which is present is preferably at least 0.05% wt, more preferably at least 0.7% wt, most preferably at least 0.1% wt.
  • The hydraulic fluid can further comprise (c) from 0.001 to 5% wt of a rust inhibitor based on total composition, preferably a carboxylic acid or ester or amide or imide containing compound, more preferably a dicarboxylic acid or its mono- or di-ester or its mono-amide or di-amide or imide, more preferably a dicarboxylic acid or its ester, amide or imide containing a total number of between 4 and 70 carbon atoms. More preferably, the number of carbon atoms of the compound is between 20 and 40. A preferred compound is an aliphatic succinimide or succinic diamide. Such compounds have been described in EP-A-776964.
  • Most preferably, (c) is from 0.001 to 5% wt of a compound according to the following formula I
    Figure US20070191237A1-20070816-C00002

    in which R1 and R2 are each hydrogen or alkyl or hydroxyalkyl of 1 to 30 carbon atoms; R3, R4 and R5 are each hydrogen or alkyl or hydroxyalkyl of 1 to 4 carbon atoms; X is CH or N and R6 and R7 are each hydrogen, alkyl or alkenyl of 1 to 30 carbon atoms, or an acyl group derived from a saturated or unsaturated carboxylic acid of up to 30 carbon atoms. Preferably, R1 and R2 are each an alkyl of from 3 to 6 carbon atoms, R3, R4 and R5 are each hydrogen, X is N and R6 and R7 are each an alkyl of 15 to 20 carbon atoms or an acyl group derived from a saturated or unsaturated dicarboxylic acid containing 4 to 10 carbon atoms, at least one of R6 and R7 being an acyl group. Especially preferred is aspartic acid, N-(3-carboxy-1-oxo-2-propenyl)-octadecyl-bis(2-methylpropyl)ester. Such aspartic acid esters are commercially available. Processes for preparing such compounds having been described in EP-A-434 464.
  • The weight ratio in which the compounds of the present invention are present, can differ within wide ranges. Preferably, the hydraulic fluid comprises magnesium salicylate, zinc dithiophosphate and optionally a rust inhibitor in such quantities that the weight ratio of magnesium salicylate to zinc dithiophosphate is from 1:5 to 1:100 and the weight ratio of magnesium salicylate to rust inhibitor is from 1:0 to 1:50.
  • The lubricant base oils present in the hydraulic fluid of the present invention, can be any base fluid which is suitable for use in hydraulic fluids. The base oil can be a natural or a synthetic lubricant base oil, or a mixture thereof. The natural oil can be an animal oil or vegetable oil, such as lard oil or castor oil, or a mineral oil such as liquid petroleum oils and solvent treated or acid treated mineral lubricating oil of the paraffinic, naphthenic, or mixed paraffinic/naphthenic type which may be further refined by hydrocracking and hydrofinishing processes and/or dewaxing. Synthetic lubricating oils include hydrocarbon oils and halo-substituted hydrocarbon oils such as polymerised and interpolymerised olefins. A suitable base oil contains poly-alpha-olefins, such as polydecene. Preferably, the base oil is a hydrocarbon base oil. More preferably, the base fluid is a mineral oil which contains less than 10% by weight of aromatic compounds, preferably less than 5% by weight, most preferably less than 3.0% by weight, measured according to DIN 51378. It is further preferred that the base oil contains less than 1.0% wt of sulphur, calculated as elemental sulphur, preferably less than 0.1% wt, more preferably less than 0.05% wt, measured according to ASTM D 4045. Such mineral oils can be prepared by severe hydroprocessing. Preferably, the lubricating oil has a kinematic viscosity in the range of from 5 to 220 cSt at 40° C., more preferably of from 10 to 200 cSt, most preferably of from 20 to 100 cSt.
  • The hydraulic fluid according to the present invention can contain further additives usually present in hydraulic fluids, such as pour point depressants, anti-foam agents and demulsifier. Pour point depressants generally are high molecular weight polymers such as alkylaromatic polymers and polymethacrylates. As anti-foam agents, silicone polymers and/or polymethacrylates are generally used. Demulsifiers which are generally applied are polyalkylene glycol ethers. Furthermore, further detergents such as sulphonates and phenates, metal deactivators, antioxidants such as phenolic compounds, diphenyl amines and phenyl naphthyl amines, ashless anti-wear agents and/or ashless dispersants, such as succinimides, can be present.
  • The hydraulic fluids of the present invention contain magnesium salicylate. For specific applications, it can be advantageous that the fluids contain a combination of magnesium and calcium salicylate.
  • The components of the present invention can be added per se to a lubricating oil, or they can be mixed into an additive package before being added to the lubricating oil. The additive package for preparing the hydraulic fluid preferably contains magnesium salicylate, zinc dithiophosphate and optionally a dicarboxylic acid or its mono- or di-ester or its mono-amide or di-amide or imide containing in total between 4 and 70 carbon atoms, wherein the weight ratio of magnesium salicylate to zinc dithiophosphate is from 1:5 to 1:100 and the weight ratio of magnesium salicylate to dicarboxylic acid or its mono- or di-ester or its mono-amide or di-amide or imide is from 1:0 to 1:50.
  • EXAMPLES
  • Formulations were prepared containing the following additives:
  • Magnesium salicylate: highly overbased magnesium alkylsalicylate having a total base number of 337 mg KOH/g (SAP 007 ex INFINEUM) and a magnesium content of about 750% of the stoichiometrically equivalent amount of magnesium based on the amount of total acid, containing 40% wt of mineral oil
  • Calcium salicylate: overbased calcium alkylsalicylate having a total base number of 168 mg KOH/g (SAP 001 ex INFINEUM), containing 40% wt of mineral oil.
  • The amounts of metal salicylate mentioned in Table 1, are the amounts of metal salicylate per se, without mineral oil.
  • Zinc dithiophosphate: zinc di(ethyl-hexyl)dithiophosphate (Elco 108 ex Elco corporation)
  • Compound according to formula I: aspartic acid, N-(3-carboxy-1-oxo-2-propenyl)-N-octadecyl , bis(2-methylpropyl)ester.
  • These compounds were added to a lubricant base oil containing less than 1.0% by weight of aromatic compounds, less than 0.05% wt of sulphur, calculated as elemental sulphur and having a kinematic viscosity in the range of 32 cSt (at 40° C.) (ISO viscosity grade 32).
  • The compositions obtained are described in Table 1. The amounts are of the compounds per se, excluding the mineral oil.
  • Compositions 1 and 2 were used in Vickers V104C vane pump tests. A new pump cartridge was used for each test. The test duration was 250 hours, performed at a fluid temperature of about 66° C., at a fluid outlet pressure of 35 bar (3.5 MPa) and at a pump speed of 1450 revolutions per minute. The results are described in Table 1.
    TABLE 1
    Composition 1 Composition 2
    magnesium salicylate 0.06% wt
    calcium salicylate 0.06% wt
    zinc dithiophosphate 0.37% wt 0.37% wt
    compound of formula I 0.10% wt 0.10% wt
    lubricant base oil balance balance
    Low load test
    ring weight loss (mg) 13 96
    vane weight loss (mg)  2  1
    total weight loss (mg) 15 97
  • From Table 1 it is clear that better protection against wear is provided by a composition containing magnesium salicylate (1), than by a composition containing calcium salicylate (2). The ring weight loss and total weight loss incurred when using composition 1 is significantly less than that incurred when composition 2 is employed. The vane weight loss is similar for both compositions

Claims (10)

1. A method for reducing total wear-induced weight loss during wear-inducing operation of hydraulic equipment, the method comprising:
a) providing a hydraulic fluid comprising a combination of an amount of zinc dithiophosphate and a quantity of magnesium salicylate, wherein said quantity of magnesium salicylate is from 0.001 to at most 1% wt and said amount of zinc dithiophosphate is from 0.01 to 1% wt.; and
b) hydraulically operating the equipment using the hydraulic fluid under wear-inducing conditions that reduce the weight of the equipment, the combination being effective to produce a first total weight loss that is less than a second total weight loss that would be observed using a second hydraulic fluid comprising a quantity of calcium salicylate in place of said quantity of magnesium salicylate.
2. The method of claim 1 wherein the first total weight loss and the second total weight loss are measured by Vickers V104C vane pump test under conditions comprising a test duration of 250 hours, a fluid temperature of about 66° C., a fluid outlet pressure of 35 bar (3.5 MPa), and a pump speed of 1450 revolutions per minute.
3. The method of claim 2 wherein the second total weight loss is six or more times greater than the first total weight loss.
4. The method of claim 1 wherein the hydraulic fluid includes a salicylate consisting essentially of magnesium salicylate.
6. The method of claim 4 wherein the magnesium salicylate has a magnesium content of more than 500% of the stoichiometrically equivalent amount of magnesium based on the amount of total acid present.
7. The method of claim 22 wherein the magnesium salicylate has a magnesium content of more than 550% of the stoichiometrically equivalent amount of magnesium based on the amount of total acid present.
8. The method of claim 1 wherein the magnesium salicylate has a magnesium content of about 750% of the stoichiometrically equivalent amount of magnesium based on the amount of total acid present.
9. The method of claim 1 wherein step a) includes including in the hydraulic fluid from 0.001 to 5% wt of a compound according to the following Formula I:
Figure US20070191237A1-20070816-C00003
in which R1 and R2 are each an alkyl of 3 to 6 carbon atoms; R3, R4 and R5 are each hydrogen; X is N and R6 and R7 are each an alkyl of 15 to 20 carbon atoms, or an acyl group derived from a saturated or unsaturated carboxylic acid containing 4 to 10 carbon atoms, at least one of R6 and R7 being an acyl group.
10. The method of claim 9 wherein step a) comprises providing a weight ratio of magnesium salicylate to zinc dithiophosphate which ranges from 1:5 to 1:100; and providing a weight ratio of magnesium salicylate to the compound of Formula I ranging from 1:0 to 1:50.
11. The method of claim 10 wherein step a) further comprises including in said hydraulic fluid at least one additive selected from the group consisting of pour point depressants, anti-foam agents, and demulsifiers.
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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112708496A (en) * 2019-12-26 2021-04-27 科之杰新材料集团有限公司 Concrete release agent for quick-drying prefabricated part and preparation method thereof

Citations (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3625893A (en) * 1967-11-06 1971-12-07 Shell Oil Co Lubricating compositions having improved oxidation stability and antirust properties
US4462918A (en) * 1982-02-17 1984-07-31 Shell Oil Company Lubricating oil composition
US4627928A (en) * 1976-08-26 1986-12-09 The Lubrizol Corporation Basic non-carbonated magnesium compositions and fuel, lubricant and additive concentrate compositions containing same
US4954273A (en) * 1987-02-27 1990-09-04 The Lubrizol Corporation Oil formulations containing overbased multi-functional additive
US5275749A (en) * 1992-11-06 1994-01-04 King Industries, Inc. N-acyl-N-hydrocarbonoxyalkyl aspartic acid esters as corrosion inhibitors
US5558802A (en) * 1995-09-14 1996-09-24 Exxon Chemical Patents Inc Multigrade crankcase lubricants with low temperature pumpability and low volatility
US5849675A (en) * 1997-04-10 1998-12-15 Chevron Chemical Company Hydraulic system using an improved antiwear hydraulic fluid
US6060437A (en) * 1997-08-01 2000-05-09 Exxon Chemical Patents, Inc. Lubricating oil compositions
US6114288A (en) * 1998-05-01 2000-09-05 Shell Research Limited Lubricating oil composition for internal combustion engines
US6306801B1 (en) * 1998-10-22 2001-10-23 Nippon Mitsubishi Oil Corporation Lubricating oil composition comprising acylated bissuccinimide, zinc dithiophosphate and metallic detergent
US6310011B1 (en) * 1994-10-17 2001-10-30 The Lubrizol Corporation Overbased metal salts useful as additives for fuels and lubricants
US6348438B1 (en) * 1999-06-03 2002-02-19 Chevron Oronite S.A. Production of high BN alkaline earth metal single-aromatic ring hydrocarbyl salicylate-carboxylate
US6569818B2 (en) * 2000-06-02 2003-05-27 Chevron Oronite Company, Llc Lubricating oil composition
US6642187B1 (en) * 1994-08-03 2003-11-04 The Lubrizol Corporation Lubricating compositions, concentrates, and greases containing the combination of an organic polysulfide and an overbased composition or a phosphorus or boron compound
US6656887B2 (en) * 2001-01-24 2003-12-02 Nippon Mitsubishi Oil Corporation Lubricating oil compositions
US7053027B2 (en) * 2000-05-09 2006-05-30 Infineum International Limited Lubricating oil compositions
US7148186B2 (en) * 1999-04-08 2006-12-12 Tonengeneral Sekiyu K.K. Lubricant oil composition for diesel engines (LAW964)

Patent Citations (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3625893A (en) * 1967-11-06 1971-12-07 Shell Oil Co Lubricating compositions having improved oxidation stability and antirust properties
US4627928A (en) * 1976-08-26 1986-12-09 The Lubrizol Corporation Basic non-carbonated magnesium compositions and fuel, lubricant and additive concentrate compositions containing same
US4462918A (en) * 1982-02-17 1984-07-31 Shell Oil Company Lubricating oil composition
US4954273A (en) * 1987-02-27 1990-09-04 The Lubrizol Corporation Oil formulations containing overbased multi-functional additive
US5275749A (en) * 1992-11-06 1994-01-04 King Industries, Inc. N-acyl-N-hydrocarbonoxyalkyl aspartic acid esters as corrosion inhibitors
US6642187B1 (en) * 1994-08-03 2003-11-04 The Lubrizol Corporation Lubricating compositions, concentrates, and greases containing the combination of an organic polysulfide and an overbased composition or a phosphorus or boron compound
US6310011B1 (en) * 1994-10-17 2001-10-30 The Lubrizol Corporation Overbased metal salts useful as additives for fuels and lubricants
US5558802A (en) * 1995-09-14 1996-09-24 Exxon Chemical Patents Inc Multigrade crankcase lubricants with low temperature pumpability and low volatility
US5849675A (en) * 1997-04-10 1998-12-15 Chevron Chemical Company Hydraulic system using an improved antiwear hydraulic fluid
US6060437A (en) * 1997-08-01 2000-05-09 Exxon Chemical Patents, Inc. Lubricating oil compositions
US6114288A (en) * 1998-05-01 2000-09-05 Shell Research Limited Lubricating oil composition for internal combustion engines
US6306801B1 (en) * 1998-10-22 2001-10-23 Nippon Mitsubishi Oil Corporation Lubricating oil composition comprising acylated bissuccinimide, zinc dithiophosphate and metallic detergent
US7148186B2 (en) * 1999-04-08 2006-12-12 Tonengeneral Sekiyu K.K. Lubricant oil composition for diesel engines (LAW964)
US6348438B1 (en) * 1999-06-03 2002-02-19 Chevron Oronite S.A. Production of high BN alkaline earth metal single-aromatic ring hydrocarbyl salicylate-carboxylate
US7053027B2 (en) * 2000-05-09 2006-05-30 Infineum International Limited Lubricating oil compositions
US6569818B2 (en) * 2000-06-02 2003-05-27 Chevron Oronite Company, Llc Lubricating oil composition
US6656887B2 (en) * 2001-01-24 2003-12-02 Nippon Mitsubishi Oil Corporation Lubricating oil compositions

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112708496A (en) * 2019-12-26 2021-04-27 科之杰新材料集团有限公司 Concrete release agent for quick-drying prefabricated part and preparation method thereof

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