WO2021198478A1 - Water-glycol hydraulic fluid composition and supplementary additive therefor - Google Patents

Water-glycol hydraulic fluid composition and supplementary additive therefor Download PDF

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Publication number
WO2021198478A1
WO2021198478A1 PCT/EP2021/058734 EP2021058734W WO2021198478A1 WO 2021198478 A1 WO2021198478 A1 WO 2021198478A1 EP 2021058734 W EP2021058734 W EP 2021058734W WO 2021198478 A1 WO2021198478 A1 WO 2021198478A1
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Prior art keywords
water
mass
glycol
hydraulic fluid
fluid composition
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PCT/EP2021/058734
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French (fr)
Inventor
Hiroshi Kaneko
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Shell Internationale Research Maatschappij B.V.
Shell Oil Company
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Application filed by Shell Internationale Research Maatschappij B.V., Shell Oil Company filed Critical Shell Internationale Research Maatschappij B.V.
Priority to CN202180026604.1A priority Critical patent/CN115397959A/en
Priority to EP21716197.5A priority patent/EP4127118B1/en
Priority to US17/910,871 priority patent/US20230144254A1/en
Priority to BR112022019775A priority patent/BR112022019775A2/en
Publication of WO2021198478A1 publication Critical patent/WO2021198478A1/en

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    • 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
    • C10M173/00Lubricating compositions containing more than 10% water
    • C10M173/02Lubricating compositions containing more than 10% water not containing mineral or fatty oils
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    • 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
    • C10M173/00Lubricating compositions containing more than 10% water
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    • 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
    • C10M105/00Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
    • C10M105/08Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen
    • C10M105/10Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M105/14Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms polyhydroxy
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    • 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
    • C10M105/00Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
    • C10M105/08Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen
    • C10M105/22Carboxylic acids or their salts
    • C10M105/24Carboxylic acids or their salts having only one carboxyl group bound to an acyclic carbon atom, cycloaliphatic carbon atom or hydrogen
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    • 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
    • C10M125/00Lubricating compositions characterised by the additive being an inorganic material
    • C10M125/10Metal oxides, hydroxides, carbonates or bicarbonates
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    • 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
    • C10M133/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
    • C10M133/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms
    • C10M133/04Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M133/06Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M133/08Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups
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    • 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
    • C10M141/00Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential
    • C10M141/06Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential at least one of them being an organic nitrogen-containing compound
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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/02Water
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    • 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
    • C10M2201/06Metal compounds
    • C10M2201/062Oxides; Hydroxides; Carbonates or bicarbonates
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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02Hydroxy compounds
    • C10M2207/021Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/022Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms containing at least two hydroxy groups
    • C10M2207/0225Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms containing at least two hydroxy groups used as base material
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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/125Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty 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
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/125Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
    • C10M2207/126Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids monocarboxylic
    • 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
    • C10M2215/042Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Alkoxylated derivatives thereof
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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/26Amines
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    • 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
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    • 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 water-glycol hydraulic fluid composition and a supplementary additive therefor.
  • the hydraulic fluid is used as a medium for transmitting power in hydraulic equipment.
  • Petroleum-based hydraulic fluids are widely used, and commonly used general hydraulic fluids use a mineral oil-based base oil such as a highly refined paraffin- based base oil.
  • a water-glycol hydraulic fluid is used as the hydraulic fluid in this equipment instead of a hydraulic fluid using a mineral oil as a base oil.
  • rust prevention is required so that hydraulic operations can be performed smoothly and the service life of hydraulic equipment can be extended.
  • a volatile, alkaline rust inhibitor must be added so that wall surfaces and ceiling surfaces not in contact with the hydraulic fluid do not rust.
  • water-glycol hydraulic fluids have excellent performance, their performance deteriorates during use due to a drop in pH and oxidation.
  • water-based hydraulic fluid compositions obtained by, for example, adding a polyoxyalkylene glycol diether compound having a specific structure, a polyoxyalkylene glycol monoether compound, a polyoxypropylene glycol monoether compound, and a fatty acid salt to water are used to improve performance in terms of pH drop suppression and oxidation stability, for example in JP 3233490 B2.
  • Water-glycol hydraulic fluids contain water and glycol as main components, but a phenomenon occurs in hydraulic equipment using these hydraulic fluids in which the water of these hydraulic fluids is vaporized during use.
  • a liquid phase or vapor phase rust inhibitor is generally used as an additive in a water-glycol hydraulic fluid, but this additive is vaporized along with the water during use and so the properties of the water-glycol hydraulic fluid may exceed their appropriate range.
  • the present invention provides a water-glycol hydraulic fluid containing 20-60% by mass water and 20-60% by mass glycol, with the remainder being, for example, a fatty acid-based lubricant, alkaline hydroxide compound, thickener, anticorrosive, and antifoaming agent to bring the total to 100% by mass.
  • a fatty acid-based lubricant for example, a fatty acid-based lubricant, alkaline hydroxide compound, thickener, anticorrosive, and antifoaming agent to bring the total to 100% by mass.
  • a specific alkanolamine compound could significantly improve the vapor phase rust prevention properties of a water- glycol hydraulic fluid, and that this alkanolamine compound could be used as an effective supplementary additive.
  • an alkanolamine compound represented by the general formula below is blended into a water-glycol hydraulic fluid.
  • Ri and R 2 are hydrocarbon groups having from 1 to 8 carbon atoms
  • R 3 is a hydrocarbon group having 2 or more carbon atoms.
  • This alkanolamine compound is also used as a supplementary additive in a water-glycol hydraulic fluid.
  • Fig. 1 is a diagram used to explain the device used to perform the vapor phase rust prevention test in the present invention.
  • a water-glycol hydraulic fluid with excellent rust prevention properties can be obtained by adding a specific alkanolamine compound.
  • this alkanolamine compound is used as a supplementary additive, the vapor phase rust prevention properties of a water-glycol-based working liquid, which decline with the vaporization of water, can be restored to the initial level of performance.
  • the alkanolamine compound of the present invention is represented by the following general formula (1).
  • Ri and R 2 represent hydrocarbon groups having from 1 to 8 carbon atoms, preferably 1-4 carbon atoms, and more preferably 3 or 4 carbon atoms. Ri and R 2 may have the same number of carbon atoms or a different number of carbon atoms. However, the same number of carbon atoms is usually preferred.
  • R 3 is a hydrocarbon group having 2 or more carbon atoms. However, because the water solubility of a compound tends to decrease as the number of carbon atoms increases, 2-4 carbon atoms are preferred.
  • alkanolamine compounds examples include N,N- dimethylaminoethanol, N,N-diethylaminoethanol, N,N- dipropylaminoethanol, N,N-dibutylaminoethanol,
  • N,N-dipentylaminoethanol N,N-dihexylaminoethanol, N,N- diheptylaminoethanol, N,N-dioctylaminoethanol, N,N- dimethylaminopropanol, N,N-diethylaminopropanol,
  • N,N-dipropylaminopropanol N,N-dibutylaminopropanol, N,N- dipentylaminopropanol, N,N-dihexylaminopropanol, N,N- diheptylaminopropanol, N,N-dioctylaminopropanol,
  • N-butyl (N-hexyl) aminopropanol, and N-butyl (N-heptyl) aminopropanol are added so that the alkali reserve of the water-glycol hydraulic fluid as specified in JIS K2234-1994 is from 10 to 25, preferably from 15 to 23, and more preferably from 18 to 21.
  • the 20°C density of these alkanolamine compounds is preferably from 0.86 to 0.89. When the density exceeds 0.89, volatility is reduced and the vapor phase rust prevention properties decline relative to the alkali reserve.
  • These alkanolamine compounds are used in water-glycol hydraulic fluid, and there are no particular restrictions on the composition of the water-glycol hydraulic fluid. However, the following composition is preferred.
  • water is 20-60% by mass, preferably 30-50% by mass
  • a fatty acid-based lubricant is 0.6-1.2% by mass
  • an alkali hydroxide compound is 0.01-0.12% by mass
  • a glycol is 20-60% by mass.
  • glycols examples include ethylene glycol, propylene glycol, butylene glycol, hexylene glycol, diethylene glycol, dipropylene glycol, dibutylene glycol, dihexylene glycol, trimethylene glycol, triethylene glycol, and tripropylene glycol. These glycols can be used alone or in mixtures of two or more. Use of propylene glycol or dipropylene glycol is preferred.
  • the amount of glycol used is 20-60% by mass, and more preferably 30-50% by mass, relative to the total mass of the water-glycol hydraulic fluid composition.
  • fatty acid-based lubricants include saturated fatty acids such as capric acid, undecylic acid, lauric acid, tridecylic acid, myristic acid, pentadecylic acid, palmitic acid, margaric acid and stearic acid, and unsaturated fatty acids such as oleic acid, linoleic acid, and linolenic acid. Sodium salts of these fatty acids can also be used.
  • Examples include sodium caprate, sodium undecylenate, sodium laurate, sodium tridecylenate, sodium myristate, sodium pentadecylate, sodium palmitate, sodium margarate, sodium stearate, sodium oleate, sodium linoleate, and sodium linolenate.
  • Dimerized fatty acids are liquid fatty acids containing a dibasic acid of a C36 dicarboxylic acid produced by dimerization of a C18 unsaturated fatty acid containing a vegetable fat or oil as a main component, but also a monobasic acid and a tribasic acid. These fatty acids, sodium salts of fatty acids, and dimerized fatty acids may be used alone or in mixtures of two or more as the fatty acid-based lubricant.
  • alkali hydroxide compounds include potassium hydroxide and sodium hydroxide. These may be used alone or together when appropriate.
  • the amount of alkaline hydroxide compound is 0.01-0.12% by mass, and more preferably 0.04-0.06% by mass, relative to the total mass of the composition.
  • a specific phosphoric acid ester compound can be used as an antiwear agent.
  • This phosphoric acid ester has the following structure.
  • R 4 and R 5 may be the same or different and represent a hydrogen atom or a hydrocarbon group having from 1 to 30 carbon atoms
  • R 6 represents a hydrocarbon group having from 1 to 20 carbon atoms
  • R 7 represents a hydrogen atom or a hydrocarbon group having from 1 to 30 carbon atoms
  • Xi, X 2
  • X3 and X4 may be the same or different and represent an oxygen atom or a sulfur atom.
  • water-glycol hydraulic fluid examples include thickeners, lubricants, metal deactivators, wear inhibitors, extreme pressure agents, dispersants, metal detergents, friction modifiers, corrosion inhibitors, anti-emulsifiers, and defoamers. These additives may be used alone or in combination with each other.
  • an additive package for water-glycol hydraulic fluids may be used.
  • An alkanolamine compound described above can be used as a supplementary additive while a water-glycol hydraulic fluid is being used.
  • a water-glycol hydraulic fluid When a new water-glycol hydraulic fluid is used, the water is vaporized, additives are vaporized along with the water, and the vapor phase rust prevention properties decline.
  • One way of determining the vapor phase rust prevention properties of a water-glycol hydraulic fluid is to measure the alkali reserve as specified in JIS K2234-1994.
  • an alkanolamine compound described above is added to a water-glycol hydraulic fluid as a supplementary additive until the initial alkali reserve has been restored.
  • a water-glycol hydraulic fluid can be used stably over a long period of time.
  • Ri and R 2 most preferably are 3 or 4 carbon atoms. This makes handling of the supplementary additive easy, and the hydraulic fluid in hydraulic equipment can be safely replenished by an on-site worker.
  • Water-glycol hydraulic fluids containing an alkanolamine compound of the present invention will now be described in detail with reference to the following non-limiting examples and comparative examples.
  • alkali reserve is determined by measuring the basic components in a water-glycol hydraulic fluid using the alkali reserve measuring method specified in JIS K2234-1994.
  • the alkali reserve indicates the amount of 0.IN hydrochloric acid in ml required to adjust the pH to 5.5 and neutralize the basic components in 10 ml of a sample oil.
  • a water-glycol hydraulic fluid was obtained by thoroughly mixing together 1.90% by mass N,N-dibutylaminoethanol as the alkanolamine compound, 37.73% by mass propylene glycol as the glycol, 16.10% by mass water-soluble polymer as the thickener, identical amounts of dimerized fatty acid and lauric acid as the fatty acid lubricants for a total of 0.80% by mass, 0.06% by mass sodium hydroxide as the alkali hydroxide compound, 1.57% by mass other additives such as a corrosion inhibitor and defoamer, and 41.84% by mass water.
  • the alkali reserve obtained in accordance with JIS K2234-1994 was 20.
  • the 40°C kinematic viscosity was 46 mm 2 /s and the pH was 11.
  • N,N-dibutylaminoethanol used here had a molecular weight of 173, a 20°C density of 0.860, a flash point of 90°C, and a boiling point of 226°C.
  • a water-glycol hydraulic fluid was obtained by thoroughly mixing together 1.00% by mass of N,N-dimethylaminoethanol as the alkanolamine compound, 38.63% by mass glycol, 16.10% by mass thickener, 0.80% by mass fatty acid lubricant, 0.06% by mass alkaline hydroxide compound, 1.57% by mass other additives, and 41.84% by mass water.
  • the alkali reserve obtained in accordance with JIS K2234-1994 was 20, and the 40°C kinematic viscosity was 46 mm 2 /s.
  • the N,N-dimethylaminoethanol used here had a molecular weight of 89, a 20°C density of 0.888, a flash point of 40°C, and a boiling point of 134°C.
  • a water-glycol hydraulic fluid was obtained by thoroughly mixing together 1.40% by mass of N-ethyldiethanolamine as the alkanolamine compound, 38.63% by mass glycol, 16.10% by mass thickener, 0.80% by mass fatty acid lubricant, 0.06% by mass alkaline hydroxide compound, 1.57% by mass other additives, and 41.84% by mass water.
  • the alkali reserve obtained in accordance with JIS K2234-1994 was 20, and the 40°C kinematic viscosity was 46 mm 2 /s.
  • the N-ethyldiethanolamine used here had a molecular weight of 133, a 20°C density of 1.07, a flash point of 124°C, and a boiling point of 251°C. Comparative Example 2
  • a water-glycol hydraulic fluid was obtained by thoroughly mixing together 1.00% by mass of N-methylethanolamine as the alkanolamine compound, 38.63% by mass glycol, 16.10% by mass thickener, 0.80% by mass fatty acid lubricant, 0.06% by mass alkaline hydroxide compound, 1.57% by mass other additives, and 41.84% by mass water.
  • the alkali reserve obtained in accordance with JIS K2234-1994 was 20, and the 40°C kinematic viscosity was 46 mm 2 /s.
  • the N-ethyldiethanolamine used here had a molecular weight of 75, a 20°C density of 0.940, a flash point of 73°C, and a boiling point of 156°C.
  • a water-glycol hydraulic fluid was obtained by thoroughly mixing together 1.00% by mass of 2-ethylaminoethanol as the alkanolamine compound, 38.23% by mass glycol, 16.10% by mass thickener, 0.80% by mass fatty acid lubricant, 0.06% by mass alkaline hydroxide compound, 1.57% by mass other additives, and 41.84% by mass water.
  • the alkali reserve obtained in accordance with JIS K2234-1994 was 20, and the 40°C kinematic viscosity was 46 mm 2 /s.
  • the 2-ethyldiaminoethanol used here had a molecular weight of 117, a 20°C density of 0.918, a flash point of 77°C, and a boiling point of 199°C.
  • a water-glycol hydraulic fluid was obtained by thoroughly mixing together 1.23% by mass of mono-n-butylethanolamine as the alkanolamine compound, 38.40% by mass glycol, 16.10% by mass thickener, 0.80% by mass fatty acid lubricant, 0.06% by mass alkaline hydroxide compound, 1.57% by mass other additives, and 41.84% by mass water.
  • the alkali reserve obtained in accordance with JIS K2234-1994 was 20, and the 40°C kinematic viscosity was 46 mm 2 /s.
  • the N-mono-n-butylethanolamine amine used here had a molecular weight of 117, a 20°C density of 0.893, a flash point of 77°C, and a boiling point of 199°C.
  • a water-glycol hydraulic fluid was obtained by thoroughly mixing together 39.63% by mass glycol, 16.10% by mass thickener, 0.80% by mass fatty acid lubricant, 0.06% by mass alkaline hydroxide compound, 1.57% by mass other additives, and 41.84% by mass water. Because an alkanolamine compound was not included the alkali reserve obtained in accordance with JIS K2234-1994 was 9, and the 40°C kinematic viscosity was 46 mm 2 /s.
  • 100 g of the water-glycol hydraulic fluid in an example or a comparative example was added to a hard glass test tube with a height of 600 mm and an outer diameter of 50 mm used in the turbine oil oxidation stability test in JIS K2514-2, and two 80 c 30 c 2 mm test pieces of rolled steel for general structures (SS-400) were suspended above and below the test tube.
  • the opening at the top of the test tube was covered with a cooler, the bottom of the test tube was placed in a constant temperature bath at 50°C, and the presence or absence of rust on the test pieces was visually confirmed after allowing the tube to stand for 200 hours.
  • Example 1 The test results are shown in Table 1.
  • Example 2 an alkanolamine compound was included so that the alkali reserve was 20.0. No rust was observed in the vapor phase rust prevention test performed on either example, and both obtained passing results. Table 1
  • Comparative Example 5 shown in Table 2, an alkanolamine compound was not included so the alkali reserve was a low 9.0, rust was observed in the vapor phase rust prevention test, and a failing result was obtained.
  • Comparative Example 2 to Comparative Example 4 an alkanolamine compound was included so that the alkali reserve was 20.0, but the alkanolamine compounds were not a dialkylaminoalkanol according to the present invention, so rust was observed in the vapor phase rust prevention test, and failing results were obtained.

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Abstract

The present invention provides a water-glycol hydraulic fluid composition comprising an alkanolamine compound according to the general formula (1), wherein the water-glycol hydraulic fluid composition comprises 20-60% by mass water, 20-60% by mass glycol, 0.6-1.2% by mass fatty acid lubricant, and 0.01-0.06% by mass alkaline hydroxide compound selected from potassium hydroxide and/or sodium hydroxide, and has an alkali reserve of 10-25, wherein R1 and R2 are hydrocarbon groups having from 1 to 8 carbon atoms, and R3 is a hydrocarbon group having 2 or more carbon atoms.

Description

WATER-GLYCOL HYDRAULIC FLUID COMPOSITION AND SUPPLEMENTARY
ADDITIVE THEREFOR
Technical Field of the Invention
The present invention relates to a water-glycol hydraulic fluid composition and a supplementary additive therefor. Background of the Invention
The hydraulic fluid is used as a medium for transmitting power in hydraulic equipment. Petroleum-based hydraulic fluids are widely used, and commonly used general hydraulic fluids use a mineral oil-based base oil such as a highly refined paraffin- based base oil.
However, because hydraulic equipment, aluminum die casting machines, and extrusion machines used in, for example, steelworks operate at high temperatures and under high pressure, there is a high risk of fire. In order to avoid the risk of fire, a water-glycol hydraulic fluid is used as the hydraulic fluid in this equipment instead of a hydraulic fluid using a mineral oil as a base oil.
When a water-based hydraulic fluid is used, rust prevention is required so that hydraulic operations can be performed smoothly and the service life of hydraulic equipment can be extended. In particular, a volatile, alkaline rust inhibitor must be added so that wall surfaces and ceiling surfaces not in contact with the hydraulic fluid do not rust. Also, while water-glycol hydraulic fluids have excellent performance, their performance deteriorates during use due to a drop in pH and oxidation. Therefore, water-based hydraulic fluid compositions obtained by, for example, adding a polyoxyalkylene glycol diether compound having a specific structure, a polyoxyalkylene glycol monoether compound, a polyoxypropylene glycol monoether compound, and a fatty acid salt to water are used to improve performance in terms of pH drop suppression and oxidation stability, for example in JP 3233490 B2.
Water-glycol hydraulic fluids contain water and glycol as main components, but a phenomenon occurs in hydraulic equipment using these hydraulic fluids in which the water of these hydraulic fluids is vaporized during use. A liquid phase or vapor phase rust inhibitor is generally used as an additive in a water-glycol hydraulic fluid, but this additive is vaporized along with the water during use and so the properties of the water-glycol hydraulic fluid may exceed their appropriate range.
In this case, it is common practice to add a supplementary additive to maintain the performance of water-glycol hydraulic fluids and keep the properties of hydraulic fluids within the appropriate range.
Therefore, it is an object of the present invention to improve the performance of water-glycol hydraulic fluids used in hydraulic equipment and to obtain a supplementary additive that can effectively maintain vapor phase rust prevention performance.
Summary of the Invention
The present invention provides a water-glycol hydraulic fluid containing 20-60% by mass water and 20-60% by mass glycol, with the remainder being, for example, a fatty acid-based lubricant, alkaline hydroxide compound, thickener, anticorrosive, and antifoaming agent to bring the total to 100% by mass. As a result of extensive research conducted to solve this problem, the present inventor and others discovered that use of a specific alkanolamine compound could significantly improve the vapor phase rust prevention properties of a water- glycol hydraulic fluid, and that this alkanolamine compound could be used as an effective supplementary additive. In the present invention, an alkanolamine compound represented by the general formula below is blended into a water-glycol hydraulic fluid.
Figure imgf000004_0002
In the general formula, Ri and R2 are hydrocarbon groups having from 1 to 8 carbon atoms, and R3 is a hydrocarbon group having 2 or more carbon atoms. This alkanolamine compound is also used as a supplementary additive in a water-glycol hydraulic fluid.
Brief Description of the Drawings
Fig. 1 is a diagram used to explain the device used to perform the vapor phase rust prevention test in the present invention.
Detailed Description of the Invention
In the present invention, a water-glycol hydraulic fluid with excellent rust prevention properties can be obtained by adding a specific alkanolamine compound. In addition, when the water in a water-glycol hydraulic fluid being used in hydraulic equipment is vaporized and this alkanolamine compound is used as a supplementary additive, the vapor phase rust prevention properties of a water-glycol-based working liquid, which decline with the vaporization of water, can be restored to the initial level of performance.
The alkanolamine compound of the present invention is represented by the following general formula (1).
Figure imgf000004_0001
Here, Ri and R2 represent hydrocarbon groups having from 1 to 8 carbon atoms, preferably 1-4 carbon atoms, and more preferably 3 or 4 carbon atoms. Ri and R2 may have the same number of carbon atoms or a different number of carbon atoms. However, the same number of carbon atoms is usually preferred. R3 is a hydrocarbon group having 2 or more carbon atoms. However, because the water solubility of a compound tends to decrease as the number of carbon atoms increases, 2-4 carbon atoms are preferred.
Examples of these alkanolamine compounds include N,N- dimethylaminoethanol, N,N-diethylaminoethanol, N,N- dipropylaminoethanol, N,N-dibutylaminoethanol,
N,N-dipentylaminoethanol, N,N-dihexylaminoethanol, N,N- diheptylaminoethanol, N,N-dioctylaminoethanol, N,N- dimethylaminopropanol, N,N-diethylaminopropanol,
N,N-dipropylaminopropanol, N,N-dibutylaminopropanol, N,N- dipentylaminopropanol, N,N-dihexylaminopropanol, N,N- diheptylaminopropanol, N,N-dioctylaminopropanol,
N,N-dimethylaminobutanol, N,N-diethylaminobutanol, N,N- dipropylaminobutanol, N,N-dibutylaminobutanol, N,N- dipentylaminobutanol, N,N-dihexylaminobutanol,
N,N-diheptylaminobutanol, N,N-dioctylaminobutanol, N-butyl (N- pentyl) aminoethanol, N-butyl (N-hexyl) amino ethanol, N-butyl (N-heptyl) aminoethanol, N-butyl (N-pentyl) aminopropanol,
N-butyl (N-hexyl) aminopropanol, and N-butyl (N-heptyl) aminopropanol. These alkanolamine compounds are added so that the alkali reserve of the water-glycol hydraulic fluid as specified in JIS K2234-1994 is from 10 to 25, preferably from 15 to 23, and more preferably from 18 to 21. The 20°C density of these alkanolamine compounds is preferably from 0.86 to 0.89. When the density exceeds 0.89, volatility is reduced and the vapor phase rust prevention properties decline relative to the alkali reserve. These alkanolamine compounds are used in water-glycol hydraulic fluid, and there are no particular restrictions on the composition of the water-glycol hydraulic fluid. However, the following composition is preferred. Relative to a total of 100% by mass, water is 20-60% by mass, preferably 30-50% by mass, a fatty acid-based lubricant is 0.6-1.2% by mass, an alkali hydroxide compound is 0.01-0.12% by mass, and a glycol is 20-60% by mass.
Examples of glycols include ethylene glycol, propylene glycol, butylene glycol, hexylene glycol, diethylene glycol, dipropylene glycol, dibutylene glycol, dihexylene glycol, trimethylene glycol, triethylene glycol, and tripropylene glycol. These glycols can be used alone or in mixtures of two or more. Use of propylene glycol or dipropylene glycol is preferred. The amount of glycol used is 20-60% by mass, and more preferably 30-50% by mass, relative to the total mass of the water-glycol hydraulic fluid composition.
Examples of fatty acid-based lubricants include saturated fatty acids such as capric acid, undecylic acid, lauric acid, tridecylic acid, myristic acid, pentadecylic acid, palmitic acid, margaric acid and stearic acid, and unsaturated fatty acids such as oleic acid, linoleic acid, and linolenic acid. Sodium salts of these fatty acids can also be used. Examples include sodium caprate, sodium undecylenate, sodium laurate, sodium tridecylenate, sodium myristate, sodium pentadecylate, sodium palmitate, sodium margarate, sodium stearate, sodium oleate, sodium linoleate, and sodium linolenate.
There are also aromatic fatty acids and dimerized fatty acids. Dimerized fatty acids are liquid fatty acids containing a dibasic acid of a C36 dicarboxylic acid produced by dimerization of a C18 unsaturated fatty acid containing a vegetable fat or oil as a main component, but also a monobasic acid and a tribasic acid. These fatty acids, sodium salts of fatty acids, and dimerized fatty acids may be used alone or in mixtures of two or more as the fatty acid-based lubricant.
Examples of alkali hydroxide compounds include potassium hydroxide and sodium hydroxide. These may be used alone or together when appropriate. The amount of alkaline hydroxide compound is 0.01-0.12% by mass, and more preferably 0.04-0.06% by mass, relative to the total mass of the composition.
A specific phosphoric acid ester compound can be used as an antiwear agent. This phosphoric acid ester has the following structure.
Figure imgf000007_0001
In this formula, R4 and R5 may be the same or different and represent a hydrogen atom or a hydrocarbon group having from 1 to 30 carbon atoms, R6 represents a hydrocarbon group having from 1 to 20 carbon atoms, R7 represents a hydrogen atom or a hydrocarbon group having from 1 to 30 carbon atoms, and Xi, X2,
X3 and X4 may be the same or different and represent an oxygen atom or a sulfur atom.
If necessary, commonly used additives may be included in the water-glycol hydraulic fluid. Examples include thickeners, lubricants, metal deactivators, wear inhibitors, extreme pressure agents, dispersants, metal detergents, friction modifiers, corrosion inhibitors, anti-emulsifiers, and defoamers. These additives may be used alone or in combination with each other. Here, an additive package for water-glycol hydraulic fluids may be used.
An alkanolamine compound described above can be used as a supplementary additive while a water-glycol hydraulic fluid is being used. When a new water-glycol hydraulic fluid is used, the water is vaporized, additives are vaporized along with the water, and the vapor phase rust prevention properties decline. One way of determining the vapor phase rust prevention properties of a water-glycol hydraulic fluid is to measure the alkali reserve as specified in JIS K2234-1994. Here, an alkanolamine compound described above is added to a water-glycol hydraulic fluid as a supplementary additive until the initial alkali reserve has been restored. When vapor phase rust prevention properties are maintained, a water-glycol hydraulic fluid can be used stably over a long period of time.
Among the alkanolamine compounds listed above, dimethylethanolamine and diethylethanolamine have been designated as toxic substances, so strict controls are required when handling them. Therefore, when used as a supplementary additive, Ri and R2 most preferably are 3 or 4 carbon atoms. This makes handling of the supplementary additive easy, and the hydraulic fluid in hydraulic equipment can be safely replenished by an on-site worker.
Examples
Water-glycol hydraulic fluids containing an alkanolamine compound of the present invention will now be described in detail with reference to the following non-limiting examples and comparative examples.
The "alkali reserve" mentioned above is determined by measuring the basic components in a water-glycol hydraulic fluid using the alkali reserve measuring method specified in JIS K2234-1994. The alkali reserve indicates the amount of 0.IN hydrochloric acid in ml required to adjust the pH to 5.5 and neutralize the basic components in 10 ml of a sample oil.
Example 1
A water-glycol hydraulic fluid was obtained by thoroughly mixing together 1.90% by mass N,N-dibutylaminoethanol as the alkanolamine compound, 37.73% by mass propylene glycol as the glycol, 16.10% by mass water-soluble polymer as the thickener, identical amounts of dimerized fatty acid and lauric acid as the fatty acid lubricants for a total of 0.80% by mass, 0.06% by mass sodium hydroxide as the alkali hydroxide compound, 1.57% by mass other additives such as a corrosion inhibitor and defoamer, and 41.84% by mass water. The alkali reserve obtained in accordance with JIS K2234-1994 was 20. The 40°C kinematic viscosity was 46 mm2/s and the pH was 11. The
N,N-dibutylaminoethanol used here had a molecular weight of 173, a 20°C density of 0.860, a flash point of 90°C, and a boiling point of 226°C.
Example 2
A water-glycol hydraulic fluid was obtained by thoroughly mixing together 1.00% by mass of N,N-dimethylaminoethanol as the alkanolamine compound, 38.63% by mass glycol, 16.10% by mass thickener, 0.80% by mass fatty acid lubricant, 0.06% by mass alkaline hydroxide compound, 1.57% by mass other additives, and 41.84% by mass water. The alkali reserve obtained in accordance with JIS K2234-1994 was 20, and the 40°C kinematic viscosity was 46 mm2/s. The N,N-dimethylaminoethanol used here had a molecular weight of 89, a 20°C density of 0.888, a flash point of 40°C, and a boiling point of 134°C.
Comparative Example 1
A water-glycol hydraulic fluid was obtained by thoroughly mixing together 1.40% by mass of N-ethyldiethanolamine as the alkanolamine compound, 38.63% by mass glycol, 16.10% by mass thickener, 0.80% by mass fatty acid lubricant, 0.06% by mass alkaline hydroxide compound, 1.57% by mass other additives, and 41.84% by mass water. The alkali reserve obtained in accordance with JIS K2234-1994 was 20, and the 40°C kinematic viscosity was 46 mm2/s. The N-ethyldiethanolamine used here had a molecular weight of 133, a 20°C density of 1.07, a flash point of 124°C, and a boiling point of 251°C. Comparative Example 2
A water-glycol hydraulic fluid was obtained by thoroughly mixing together 1.00% by mass of N-methylethanolamine as the alkanolamine compound, 38.63% by mass glycol, 16.10% by mass thickener, 0.80% by mass fatty acid lubricant, 0.06% by mass alkaline hydroxide compound, 1.57% by mass other additives, and 41.84% by mass water. The alkali reserve obtained in accordance with JIS K2234-1994 was 20, and the 40°C kinematic viscosity was 46 mm2/s. The N-ethyldiethanolamine used here had a molecular weight of 75, a 20°C density of 0.940, a flash point of 73°C, and a boiling point of 156°C.
Comparative Example 3
A water-glycol hydraulic fluid was obtained by thoroughly mixing together 1.00% by mass of 2-ethylaminoethanol as the alkanolamine compound, 38.23% by mass glycol, 16.10% by mass thickener, 0.80% by mass fatty acid lubricant, 0.06% by mass alkaline hydroxide compound, 1.57% by mass other additives, and 41.84% by mass water. The alkali reserve obtained in accordance with JIS K2234-1994 was 20, and the 40°C kinematic viscosity was 46 mm2/s. The 2-ethyldiaminoethanol used here had a molecular weight of 117, a 20°C density of 0.918, a flash point of 77°C, and a boiling point of 199°C.
Comparative Example 4
A water-glycol hydraulic fluid was obtained by thoroughly mixing together 1.23% by mass of mono-n-butylethanolamine as the alkanolamine compound, 38.40% by mass glycol, 16.10% by mass thickener, 0.80% by mass fatty acid lubricant, 0.06% by mass alkaline hydroxide compound, 1.57% by mass other additives, and 41.84% by mass water. The alkali reserve obtained in accordance with JIS K2234-1994 was 20, and the 40°C kinematic viscosity was 46 mm2/s. The N-mono-n-butylethanolamine amine used here had a molecular weight of 117, a 20°C density of 0.893, a flash point of 77°C, and a boiling point of 199°C.
Comparative Example 5
A water-glycol hydraulic fluid was obtained by thoroughly mixing together 39.63% by mass glycol, 16.10% by mass thickener, 0.80% by mass fatty acid lubricant, 0.06% by mass alkaline hydroxide compound, 1.57% by mass other additives, and 41.84% by mass water. Because an alkanolamine compound was not included the alkali reserve obtained in accordance with JIS K2234-1994 was 9, and the 40°C kinematic viscosity was 46 mm2/s.
Tests
The vapor phase rust prevention properties of the examples and comparative examples were evaluated as follows.
Vapor Phase Rust Prevention Test
As shown in Fig. 1, 100 g of the water-glycol hydraulic fluid in an example or a comparative example was added to a hard glass test tube with a height of 600 mm and an outer diameter of 50 mm used in the turbine oil oxidation stability test in JIS K2514-2, and two 80 c 30 c 2 mm test pieces of rolled steel for general structures (SS-400) were suspended above and below the test tube. The opening at the top of the test tube was covered with a cooler, the bottom of the test tube was placed in a constant temperature bath at 50°C, and the presence or absence of rust on the test pieces was visually confirmed after allowing the tube to stand for 200 hours.
Evaluation Standards:
Rust was observed on neither test piece Passed
Rust was observed on one or both test pieces Failed
The test results are shown in Table 1. In Example 1 and Example 2 shown in Table 1, an alkanolamine compound was included so that the alkali reserve was 20.0. No rust was observed in the vapor phase rust prevention test performed on either example, and both obtained passing results. Table 1
Figure imgf000012_0001
In Comparative Example 5 shown in Table 2, an alkanolamine compound was not included so the alkali reserve was a low 9.0, rust was observed in the vapor phase rust prevention test, and a failing result was obtained. In Comparative Example 2 to Comparative Example 4, an alkanolamine compound was included so that the alkali reserve was 20.0, but the alkanolamine compounds were not a dialkylaminoalkanol according to the present invention, so rust was observed in the vapor phase rust prevention test, and failing results were obtained.
Table 2
Figure imgf000013_0001

Claims

C LA IM S
1. A water-glycol hydraulic fluid composition comprising an alkanolamine compound according to the general formula (1), wherein the water-glycol hydraulic fluid composition comprises 20-60% by mass water, 20-60% by mass glycol, 0.6-1.2% by mass fatty acid lubricant, and 0.01-0.06% by mass alkaline hydroxide compound selected from potassium hydroxide and/or sodium hydroxide, and has an alkali reserve of 10-25,
Figure imgf000014_0001
wherein Ri and R2 are hydrocarbon groups having from 1 to 8 carbon atoms, and R3 is a hydrocarbon group having 2 or more carbon atoms.
2. A water-glycol hydraulic fluid composition according to claim wherein the alkanolamin according to general formula (1) is N,N- dibutylaminoethanol.
3. A method for adjusting the alkali reserve of a water-glycol hydraulic fluid composition, said method comprising the addition of a supplementary additive comprising a alkanolamine of general formula (1) to the water-glycol hydraulic fluid to adjust the alkali reserve of the water-glycol hydraulic fluid composition to 10-25 during use
Figure imgf000014_0002
wherein Ri and R2 are hydrocarbon groups having from 1 to 8 carbon atoms, and R3 is a hydrocarbon group having 2 or more carbon atoms.
4. A method according to Claim 3, wherein the alkanolamine is N,N-dibutylaminoethanol.
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Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3280029A (en) * 1964-06-18 1966-10-18 Mobil Oil Corp Lubricant compositions
JP3233490B2 (en) 1993-03-29 2001-11-26 株式会社コスモ総合研究所 Hydrated hydraulic fluid composition
WO2009012058A2 (en) * 2007-07-18 2009-01-22 Dow Global Technologies Inc. Water-glycol hydraulic fluid compositions

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4151099A (en) * 1977-01-03 1979-04-24 Basf Wyandotte Corporation Water-based hydraulic fluid and metalworking lubricant
US4390439A (en) * 1981-03-30 1983-06-28 Basf Wyandotte Corporation Water-based hydraulic fluids having improved lubricity and corrosion inhibiting properties employing neodecanoic acid
MX169073B (en) * 1986-12-30 1993-06-21 Union Carbide Corp ENERGY TRANSMITTER FLUID
JP3659765B2 (en) * 1997-05-20 2005-06-15 株式会社キレスト技研 Metal anticorrosive composition
KR101435563B1 (en) * 2006-05-05 2014-08-29 엥거스 케미칼 캄파니 Metalworking fluids comprising neutralized fatty acids
JP2009040813A (en) * 2007-08-06 2009-02-26 Cosmo Oil Co Ltd Method of controlling content of vapor phase rust inhibitor in water-containing lubricant
EP2331666A2 (en) * 2008-08-28 2011-06-15 BASF Corporation Hydraulic fluid and method of preventing vapor corrosion
WO2015031052A2 (en) * 2013-08-31 2015-03-05 Houghton Technical Corp. Hydraulic fluid compositions
JP6296943B2 (en) * 2014-08-28 2018-03-20 コスモ石油ルブリカンツ株式会社 Hydrous hydraulic fluid

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3280029A (en) * 1964-06-18 1966-10-18 Mobil Oil Corp Lubricant compositions
JP3233490B2 (en) 1993-03-29 2001-11-26 株式会社コスモ総合研究所 Hydrated hydraulic fluid composition
WO2009012058A2 (en) * 2007-07-18 2009-01-22 Dow Global Technologies Inc. Water-glycol hydraulic fluid compositions

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