US20080171680A1 - Composition of water-soluble metalworking fluid using distillation residue generated in production of biodiesel - Google Patents

Composition of water-soluble metalworking fluid using distillation residue generated in production of biodiesel Download PDF

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US20080171680A1
US20080171680A1 US11/974,591 US97459107A US2008171680A1 US 20080171680 A1 US20080171680 A1 US 20080171680A1 US 97459107 A US97459107 A US 97459107A US 2008171680 A1 US2008171680 A1 US 2008171680A1
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oil
biodiesel
water
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distillation residue
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Kwang Soon Kim
Jae Min Cha
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Korea Houghton Corp
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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
    • C10M109/00Lubricating compositions characterised by the base-material being a compound of unknown or incompletely defined constitution
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    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M101/00Lubricating compositions characterised by the base-material being a mineral or fatty oil
    • C10M101/04Fatty oil fractions
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    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M127/00Lubricating compositions characterised by the additive being a non- macromolecular hydrocarbon
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    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M169/00Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
    • C10M169/04Mixtures of base-materials and additives
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    • 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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    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M177/00Special methods of preparation of lubricating compositions; Chemical modification by after-treatment of components or of the whole of a lubricating composition, not covered by other classes
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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
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/281Esters of (cyclo)aliphatic monocarboxylic acids
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/281Esters of (cyclo)aliphatic monocarboxylic acids
    • C10M2207/2815Esters of (cyclo)aliphatic monocarboxylic acids used as base material
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/40Fatty vegetable or animal oils
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    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/10Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/103Polyethers, i.e. containing di- or higher polyoxyalkylene groups
    • C10M2209/104Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing two carbon atoms only
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    • 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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    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/22Heterocyclic nitrogen compounds
    • C10M2215/223Five-membered rings containing nitrogen and carbon only
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    • C10M2229/00Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
    • C10M2229/02Unspecified siloxanes; Silicones
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    • C10N2020/00Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
    • C10N2020/01Physico-chemical properties
    • C10N2020/081Biodegradable compounds
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    • 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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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/64Environmental friendly compositions
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    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/20Metal working
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    • C10N2050/00Form in which the lubricant is applied to the material being lubricated
    • C10N2050/01Emulsions, colloids, or micelles
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    • C10N2070/00Specific manufacturing methods for lubricant compositions

Definitions

  • the present invention relates to a water-soluble metalworking fluid used in metal machining, and more particularly, to a composition of a water-soluble metalworking fluid produced by adding 5 to 70 wt % of additives to 20 to 95 wt % of distillation residues that is generated in production of biodiesel and used as lubricating base oil, and 0 to 40 wt % of ion exchange water.
  • Metalworking fluids are fluids which are used to assist metal machining operations. Traditional metal machining requires a machine tool, a cutting tool, a worked metal, and a machining fluid. Metalworking fluids were first used to increase the lifespan of an instrument for metal processing in the early 1900s.
  • the original metalworking fluids were mainly formed of base oil refined from crude oil, and contained a large amount of polyaromatic hydrocarbons (PAHs) that are now known to be carcinogens due to non-development of refinement techniques. Workers can be exposed to these metalworking fluids via many forms and paths while in use, and the fluids may be a cause of cancer, non-malignant respiratory disease, dermatosis, microbial disease, etc. for the workers. Problems caused by oil mists and metalworking fluids were so significant for industrial health that they were even one of the priorities chosen by the U.S. Occupational Safety and Health Administration (OSHA) in 1996.
  • PHAs polyaromatic hydrocarbons
  • the metalworking fluids reduce friction and abrasion between a cutting tool and a worked metal, improve machining surface characteristics, reduce adhesion or melting of the surface, remove generated heat, prevent deformation caused by heat, and wash cut pieces, fine powder and residues.
  • the metalworking fluids also prevent corrosion of machined surfaces, and cool the heated machined surfaces down so as to be more easily handled.
  • the water-soluble metalworking fluids include cooling, prevention of welding between the cutting tool and the machined surfaces, prevention of abrasion at high temperature, and prevention of distortion caused by remaining heat.
  • the water-soluble metalworking fluids are diluted with a water of about 60 to 85% just before using base oil that is more highly refined than cycloparaffin or paraffin-based oils used in a non-water-soluble environment. Since an available concentration of the water-soluble fluid ranges from 1 to 10%, characteristics of water that is used as a base material are important to performance of the fluid. Water is the best cooling agent due to high specific heat, good thermal conductivity and high latent heat. However, water rusts metal, and thus has less wettability and lubrication than oil.
  • the water-soluble metalworking fluids include a rust inhibitor or a surfactant, thereby increasing lubrication.
  • a recently developed additive can prevent corrosion for approximately several days to a week, which thus overcomes the poor rust inhibition and poor metal corrosion inhibition of the water-soluble metalworking fluids.
  • the water-soluble metalworking fluids are nonflammable like water and non-sticky, so it is preferred by workers due to a clean work environment, but it is corruptible.
  • the advantages of the water-soluble metalworking fluids are as follows. It can be used for fast cutting due to good cooling properties, and cleansing, thereby providing safe conditions for workers. Also, it is economical because of the use of water.
  • the water-soluble metalworking fluids are classified into two types, which are an emulsion type which is translucent to an emulsion like a milky liquid when diluted with water, and a semi-synthetic and synthetic type.
  • the milky white residue of the dilution indicates that an emulsion particle has a sufficient size to reflect transmitted light, and the clear dilution indicates that the particle is so small that the transmitted light mostly penetrates between the particles.
  • Components and ratios of the conventional water-soluble metalworking fluids are listed below.
  • the present invention is directed to developing a composition of a water-soluble metalworking fluid using a distillation residue generated in production of biodiesel as environmentally-friendly lubricating base oil.
  • Biodiesel refers to an alternative energy processed from elemental lipid in vegetables and animals to have similar properties to gasoline, which can be used as a diesel equivalent or for diesel engines by being mixed with the gasoline.
  • biodiesel refers to fatty acid methyl esters having a purity of 95% made from the transesterification between alcohols (generally, methanol) and vegetable oil (rice bran, waste cooking oil, soybean oil, rape oil, etc.). (Ministry of Commerce, Industry and Economy (MOCIE) Announcement No. 2000-57)
  • the vegetable oil described above that is, a compound including a hydrophobic group insoluble in water, is generally composed of triglycerides represented as the following chemical structural formula.
  • the vegetable oil is commonly characterized by the content of the fatty acid, and the length, content and saturation degree of the fatty acid become critical factors in determining physical and chemical characteristics of the oil.
  • Animal oil is less useful than the vegetable oil, and only that made from a pig, a cow and a sheep among land animals, and herring and menhaden among fishes are considered as being commercially important.
  • the animal oils are composed of saturated and unsaturated triglycerides like the vegetable oils, but include a wide distribution of fatty acids and some odd-numbered chain fatty acids, unlike the vegetable oils.
  • the methyl ester from vegetable oil is mainly made of methyl oleate and methyl linoleate as main components, and exhibits excellent performance in machinability or detergency due to low viscosity (40 ⁇ , 1.9 to 6.0 cSt.) and good lubrication when used instead of petroleum-based hydrocarbon lubricating base oil.
  • the methyl ester from vegetable oil is made by the following processes.
  • R, R′ and R′′ are saturated or unsaturated hydrocarbons with alkyl groups.
  • the methyl ester made from vegetable oil has various components and composition ratios depending on components of fatty acid in the vegetable oil and its ratio.
  • Each of the methyl esters of the fatty acids listed in the following table is a component of the methyl ester made from vegetable oil.
  • Vegetable oils capable of synthesizing the methyl esters from vegetable oil which may be used in the present invention are listed in the following table.
  • Biodiesel may be mixed with gasoline and then used, or 100% pure biodiesel may be used.
  • BD5 refers to a mixture of 95% gasoline and 5% biodiesel
  • BD20 refers to a mixture including 20% biodiesel.
  • Biodiesel attracts attention around the world as a future energy source in the aspects of recycling of waste resources, reduction of greenhouse gas (CO 2 ), and low emission of air pollutants.
  • CO 2 greenhouse gas
  • biodiesel is in exemplary use or is expanding its supply through model projects all over the world. Europe, which is very positive towards the use of alternative energy, first established a system for biodiesel.
  • biodiesel can be used within a range satisfying the standard of general gasoline, and according to European Fuel Standard (EN590) taken effect in January, 2004, gasoline including 5% biodiesel or less (BD5) is recognized as general gasoline (satisfying the requirements of the EN14214 standard).
  • EN590 European Fuel Standard
  • BD5 gasoline including 5% biodiesel or less
  • BD5 European Fuel Standard
  • U.S. after National Biodiesel Board was founded in 1992, the Congress and EPA approved BD20 as a fuel for diesel engine vehicles in 1998, and President Bush declared the expansion of new recycled energy including biodiesel in 2001.
  • the supply of biodiesel is increasing every year, and biodiesel is used in official vehicles of state governments and buses in addition to the U.S. Army, the U.S. Air Force, the Department of Energy and NASA.
  • biodiesel In Korea, based on the announcement regarding a model supply project for biodiesel by MOCCC in May, 2002, the government performed the project for two years, and now is investigating market reaction to and problems with biodiesel.
  • the major advantage of biodiesel is a reduction of smoke emitted from vehicles.
  • biodiesel also emits the greenhouse gas CO 2 , when viewed from an overall cycle of the process (from production to consumption) it yields very low amounts of CO 2 , and emits relatively low amounts of sulfur oxide (Sox) and particulate matters (PMs).
  • Biodiesel made from vegetable resources may be self-produced domestically, which is an advantage for energy security, and may reduce environmental pollution by recycling waste resources, such as waste cooking oil.
  • biodiesel has several problems in substituting for conventional gasoline and volatile oils. Although biodiesel has to be mixed in a high ratio to reduce toxic chemicals in exhaust gases from vehicles, it may break down engines due to corrosion, and become denatured in long-term storage.
  • methyl esters made from vegetable oil are required for methyl esters made from vegetable oil to be used as fuel oils for vehicles, and thus a separate vacuum distillation process is performed after the reaction of methyl esters.
  • the vacuum distillation is performed at 2 to 3 torrs and a maximum temperature of 240 ⁇ .
  • the distilled result is used as biodiesel fuel oil, and a distillation residue of about 10% is scrapped.
  • Such a distillation residue generated in the production of biodiesel is a reactant of the vegetable oil with a structure of ester, and may be used as environmentally friendly lubricating base oil.
  • An embodiment of the invention provides a composition of a water-soluble metalworking fluid which uses a distillation residue generated in production of biodiesel as lubricating oil, and is mixed with other additives.
  • the additives include a surfactant, a lubricating additive, a metal corrosion inhibitor, a rust inhibitor, a pH booster, a defoamer, a preservative, a pigment, etc., of which all are less harmful to the environment, and do not include any one of components which have use restrictions, such as nitrite, formaldehyde, boron and derivatives thereof, and an extreme pressure agent.
  • the present invention is directed to a composition of a water-soluble metalworking fluid produced by adding 5 to 70 wt % of additives to 20 to 95 wt % of distillation residues that is generated in production of biodiesel and used as lubricating base oil, and 0 to 40 wt % of ion exchange water.
  • the distillation residue of the biodiesel is generated from canola oil, soybean oil, palm oil or jatropha oil.
  • the additive used in the present invention is at least one selected from the group consisting of a surfactant, a lubricating additive, a metal corrosion inhibitor, a rust inhibitor, a pH booster, a defoamer and a preservative.
  • the surfactant used in the present invention is selected from ethoxide of lauryl alcohol or oleyl alcohol, ethoxide of castor oil, ethoxide of laurylamine or oleylamine, amine salt of oleic acid, amine salt of tall oil, amine salt of erucic acid, sulfonate, Hypermer A 70, Targat V 20, Veg Ester GY-112, Addconate H, Addconate M, succinic acid derivatives, amine salt of succinic acid and PEG-fatty acid ester.
  • the lubricating base oil used in the present invention is at least one selected from the group consisting of petroleum-based hydrocarbon, vegetable oil and synthetic ester.
  • the petroleum-based hydrocarbon is a distilled mineral oil and has a kinematic viscosity of about 5 to 1000 cSt at 40 ⁇
  • the vegetable oil and the synthetic ester are soybean oil, canola oil, sunflower oil, jatropha oil, palm oil, neopentyl glycol dioleate, trimethylolpropane trioleate, pentaerythritol tetraoleate, propylene glycol dioleate, ricinoleic acid condensate, or methyl ester of soybean oil, canola oil, jatropha oil or palm oil.
  • the pH booster used in the present invention includes monoethanolamine, diethanolamine, triethanolamine, monoisopropanolamine, diisopropanolamine, triisopropanolamine, aminomethyl propanol or diglycolamine.
  • the metal corrosion inhibitor used in the present invention includes benzotriazol, tolytriazol or derivatives thereof
  • the rust inhibitor used in the present invention includes sebacic acid, Corfree M1, Irgacor 190 plus or derivatives thereof
  • the defoamer used in the present invention includes polydimethyl siloxane, denatured polydimethyl siloxane, organic silicon derivatives or a silicon-based defoamer of silica.
  • the preservative used in the present invention includes thiazoline, pyridine, morpholine, phenol, a nitro- or IPBC-based preservative.
  • Water-soluble metalworking fluids were manufactured from a distillation residue generated in production of biodiesel, ion exchange water, a lubricating additive 1 (soybean oil, canola oil, palm oil, trimethylolpropane trioleate, pentaerythritol tetraoleate, or ricinoleic acid condensate), a surfactant, a metal corrosion inhibitor, a rust inhibitor, a pH booster, a defoamer and a preservative.
  • Contents of the water and the biodiesel distillation residue depend on application ranges of the product. As the product has a higher content of water, the diluted solution is clearer, while as the product has a higher content of the distillation residue, the diluted solution is milky white and has better lubrication performance.
  • Water-soluble metalworking fluids were produced from a distillation residue generated in production of biodiesel, a lubricating additive 2 (petroleum-based hydrocarbon, methyl ester of soybean oil or canola oil, soybean oil, canola oil, or palm oil), a surfactant, a metal corrosion inhibitor, a rust inhibitor, a pH booster, a defoamer and a preservative.
  • Water-soluble metalworking fluids were produced from a distillation residue generated in production of biodiesel, a lubricating additive 3 (petroleum-based hydrocarbon, methyl ester of soybean oil, canola oil or palm oil, trimethylolpropane trioleate, pentaerythritol tetraoleate or ricinoleic acid condensate), a surfactant, a metal corrosion inhibitor, a rust inhibitor, a pH booster, a defoamer and a preservative.
  • a lubricating additive 3 mineral oil-based hydrocarbon, methyl ester of soybean oil, canola oil or palm oil, trimethylolpropane trioleate, pentaerythritol tetraoleate or ricinoleic acid condensate
  • a surfactant a metal corrosion inhibitor
  • rust inhibitor a rust inhibitor
  • pH booster a defoamer and a preservative.
  • Water-soluble metalworking fluids were produced from a distillation residue generated in production of biodiesel, a lubricating additive 4 (methyl ester of soybean oil, canola oil, jatropha oil or palm oil, soybean oil, canola oil, palm oil, jatropha oil or sunflower oil), a surfactant, a metal corrosion inhibitor, a rust inhibitor, a pH booster, a defoamer and a preservative.
  • a lubricating additive 4 methyl ester of soybean oil, canola oil, jatropha oil or palm oil, soybean oil, canola oil, palm oil, jatropha oil or sunflower oil
  • a surfactant methyl ester of soybean oil, canola oil, jatropha oil or palm oil, soybean oil, canola oil, palm oil, jatropha oil or sunflower oil
  • a surfactant methyl ester of soybean oil, canola oil, jatropha oil or palm oil, soybean oil, canola oil, palm oil, jatropha oil or sunflower oil
  • a composition of a water-soluble metalworking fluid, using a biodiesel distillation residue that can be used as environmentally acceptable lubricating base oil, has good biodegradation, excellent lubrication and less toxicity bionomically.
  • the water-soluble metalworking fluid may be very useful in business and recycling resources.

Abstract

A composition of a water-soluble metalworking fluid used in metal machining is formed by adding 5 to 70 wt % additive to 5 to 95 wt % distillation residues that is generated in production of biodiesel and used as lubricating base oil, and 0 to 70 wt % ion exchange water.

Description

    CROSS-REFERENCE TO RELATED APPLICATION
  • This application claims the benefit of Korean Patent Application No. 10-2007-0003692, filed on Jan. 12, 2007, the disclosure of which is hereby incorporated herein by reference in its entirety.
  • BACKGROUND OF THE INVENTION
  • 1. Field of the Invention
  • The present invention relates to a water-soluble metalworking fluid used in metal machining, and more particularly, to a composition of a water-soluble metalworking fluid produced by adding 5 to 70 wt % of additives to 20 to 95 wt % of distillation residues that is generated in production of biodiesel and used as lubricating base oil, and 0 to 40 wt % of ion exchange water.
  • 2. Description of the Related Art
  • Metalworking fluids are fluids which are used to assist metal machining operations. Traditional metal machining requires a machine tool, a cutting tool, a worked metal, and a machining fluid. Metalworking fluids were first used to increase the lifespan of an instrument for metal processing in the early 1900s. The original metalworking fluids were mainly formed of base oil refined from crude oil, and contained a large amount of polyaromatic hydrocarbons (PAHs) that are now known to be carcinogens due to non-development of refinement techniques. Workers can be exposed to these metalworking fluids via many forms and paths while in use, and the fluids may be a cause of cancer, non-malignant respiratory disease, dermatosis, microbial disease, etc. for the workers. Problems caused by oil mists and metalworking fluids were so significant for industrial health that they were even one of the priorities chosen by the U.S. Occupational Safety and Health Administration (OSHA) in 1996.
  • These days, according to the characteristics of metal machining, various kinds of metalworking fluids are produced and various kinds of additives are used. The amount and composition of the additives depend on the kind of the metalworking fluids and the characteristics of the product.
  • The metalworking fluids reduce friction and abrasion between a cutting tool and a worked metal, improve machining surface characteristics, reduce adhesion or melting of the surface, remove generated heat, prevent deformation caused by heat, and wash cut pieces, fine powder and residues. In addition, the metalworking fluids also prevent corrosion of machined surfaces, and cool the heated machined surfaces down so as to be more easily handled.
  • Functions of the water-soluble metalworking fluids include cooling, prevention of welding between the cutting tool and the machined surfaces, prevention of abrasion at high temperature, and prevention of distortion caused by remaining heat. The water-soluble metalworking fluids are diluted with a water of about 60 to 85% just before using base oil that is more highly refined than cycloparaffin or paraffin-based oils used in a non-water-soluble environment. Since an available concentration of the water-soluble fluid ranges from 1 to 10%, characteristics of water that is used as a base material are important to performance of the fluid. Water is the best cooling agent due to high specific heat, good thermal conductivity and high latent heat. However, water rusts metal, and thus has less wettability and lubrication than oil. To overcome these disadvantages, the water-soluble metalworking fluids include a rust inhibitor or a surfactant, thereby increasing lubrication. A recently developed additive can prevent corrosion for approximately several days to a week, which thus overcomes the poor rust inhibition and poor metal corrosion inhibition of the water-soluble metalworking fluids.
  • The water-soluble metalworking fluids are nonflammable like water and non-sticky, so it is preferred by workers due to a clean work environment, but it is corruptible.
  • The advantages of the water-soluble metalworking fluids are as follows. It can be used for fast cutting due to good cooling properties, and cleansing, thereby providing safe conditions for workers. Also, it is economical because of the use of water.
  • The water-soluble metalworking fluids are classified into two types, which are an emulsion type which is translucent to an emulsion like a milky liquid when diluted with water, and a semi-synthetic and synthetic type. The milky white residue of the dilution indicates that an emulsion particle has a sufficient size to reflect transmitted light, and the clear dilution indicates that the particle is so small that the transmitted light mostly penetrates between the particles. Components and ratios of the conventional water-soluble metalworking fluids are listed below.
  • Emulsion Semi-Synthetic Synthetic
    Kind of Additive Type Type Type
    Emulsifier 20~30%  20~30% 
    Lubricating Additive/ 0~40% 0~10% 0~30%
    Extreme Pressure Additive
    pH booster 3~10% 3~10% 10~25% 
    (Amines, etc.)
    Metal Corrosion Inhibitor  1~5%  1~5%  1~8%
    Preservative  0~3%  2~4%  0~3%
    Defoamer  0~2%  0~2% 0~0.5% 
    Lubricating Base Oil ~100% 5~30%
    Ion Exchange Water ~100% ~100%
  • Recently, as interest in the importance of environmental protection and health and safety for workers has been increasing around the whole world, research on environmentally-acceptable lubricating base oil which will substitute for hydrocarbon-based lubricating base oil among the metalworking fluids is progressing in North American and Western European nations.
  • The present invention is directed to developing a composition of a water-soluble metalworking fluid using a distillation residue generated in production of biodiesel as environmentally-friendly lubricating base oil.
  • Biodiesel refers to an alternative energy processed from elemental lipid in vegetables and animals to have similar properties to gasoline, which can be used as a diesel equivalent or for diesel engines by being mixed with the gasoline. In general, biodiesel refers to fatty acid methyl esters having a purity of 95% made from the transesterification between alcohols (generally, methanol) and vegetable oil (rice bran, waste cooking oil, soybean oil, rape oil, etc.). (Ministry of Commerce, Industry and Economy (MOCIE) Announcement No. 2000-57)
  • The vegetable oil described above, that is, a compound including a hydrophobic group insoluble in water, is generally composed of triglycerides represented as the following chemical structural formula.
  • Figure US20080171680A1-20080717-C00001
  • The vegetable oil is commonly characterized by the content of the fatty acid, and the length, content and saturation degree of the fatty acid become critical factors in determining physical and chemical characteristics of the oil. Animal oil is less useful than the vegetable oil, and only that made from a pig, a cow and a sheep among land animals, and herring and menhaden among fishes are considered as being commercially important. The animal oils are composed of saturated and unsaturated triglycerides like the vegetable oils, but include a wide distribution of fatty acids and some odd-numbered chain fatty acids, unlike the vegetable oils.
  • When methyl ester made from vegetable oil, that is, biodiesel, is spilled on soil, the soil is less polluted than by hydrocarbon-base lubricating base oil, because of lower toxicity and higher biodegradation. Also, corresponding to United Nations Framework Convention on Climate Change (UNFCCC) (Life cycle CO2: ¼ of gasoline), one(1) ton of the methyl ester from vegetable oil cuts 2.2 tons of CO2, which contributes to an increase in global competitiveness. The methyl ester from vegetable oil is mainly made of methyl oleate and methyl linoleate as main components, and exhibits excellent performance in machinability or detergency due to low viscosity (40□, 1.9 to 6.0 cSt.) and good lubrication when used instead of petroleum-based hydrocarbon lubricating base oil.
  • CH3—(CH2)14—COO—CH3: Methyl Palmitate CH3—(CH2)6—CH2—CH═CH—CH2—(CH2)6—COO—CH3: Methyl Oleate CH3—(CH2)3—CH2—CH═CH—CH2—CH═CH—CH2—(CH2)6—COO—CH3: Methyl Linoleate
  • The methyl ester from vegetable oil is made by the following processes.
  • <Transesterification>
  • Figure US20080171680A1-20080717-C00002
  • <Esterification>

  • R—COOH+CH3OH→R—COO CH3
  • Catalyst
  • Here, R, R′ and R″ are saturated or unsaturated hydrocarbons with alkyl groups.
  • The methyl ester made from vegetable oil has various components and composition ratios depending on components of fatty acid in the vegetable oil and its ratio. Each of the methyl esters of the fatty acids listed in the following table is a component of the methyl ester made from vegetable oil.
  • <Chemical Structure of Fatty Acid Used in Water-Soluble Metalworking Fluid and Formation of Methyl Ester Made From Vegetable Oil>
  • Carbon Number/
    Name of Double Bond
    Fatty Acid Number Chemical Structure
    Caprylic C8 CH3(CH2)6COOH
    Capric C10 CH3(CH2)8COOH
    Lauric C12 CH3(CH2)10COOH
    Myristric C14 CH3(CH2)12COOH
    Palmitic C16:0 CH3(CH2)14COOH
    Palmitoleic C16:1 CH3(CH2)5CH═CH(CH2)7COOH
    Stearic C18:0 CH3(CH2)16COOH
    Oleic C18:1 CH3(CH2)7CH═CH(CH2)7COOH
    Linoleic C18:2 CH3(CH2)4CH═CHCH2CH═CH(CH2)7COOH
    Linolenic C18:3 CH3(CH2)2CH═CHCH2CH═CHCH2CH═CH(CH2)7COOH
    Arachidic C20:0 CH3(CH2)18COOH
    Eicosenoic C20:1 CH3(CH2)7CH═CH(CH2)9COOH
    Behenic C22:0 CH3(CH2)20COOH
    Erucic C22:1 CH3(CH2)7CH═CH(CH2)11COOH
  • Vegetable oils capable of synthesizing the methyl esters from vegetable oil which may be used in the present invention are listed in the following table.
  • <Fatty Acid Components of Vegetable Oil Used in Formation of Biodiesel>
  • Fatty acid,
    Fatty oil C20:0 C20:1
    and oil C8:0 C10:0 C14:0 C16:0 C16:1 C18:0 C18:1 C18:2 C18:3 C22:0 C22:1
    Coconut oil 5-9 4-10 44-51 13-18  7-10 1-4 5-8 1-3
    Palm 2-4 3-7  45-52 14-19 6-9 0-1 1-3 10-18 1-2 1-2 
    Kernal Oil
    Palm Oil 1-6 32-47 1-6 40-52  2-11
    Soybean 0.3  7-11 0-1 3-6 22-34 50-60 2-10 5-10
    Oil
    Jatropha Oil 35-50  0-10 30-40  5-15
    Canola Oil 2-5 0.2 1-2 10-15 10-20 5-10 0.9 50-60
  • Biodiesel may be mixed with gasoline and then used, or 100% pure biodiesel may be used. BD5 refers to a mixture of 95% gasoline and 5% biodiesel, and BD20 refers to a mixture including 20% biodiesel. Biodiesel attracts attention around the world as a future energy source in the aspects of recycling of waste resources, reduction of greenhouse gas (CO2), and low emission of air pollutants. Recently, biodiesel is in exemplary use or is expanding its supply through model projects all over the world. Europe, which is very positive towards the use of alternative energy, first established a system for biodiesel. Europe recognizes that biodiesel can be used within a range satisfying the standard of general gasoline, and according to European Fuel Standard (EN590) taken effect in January, 2004, gasoline including 5% biodiesel or less (BD5) is recognized as general gasoline (satisfying the requirements of the EN14214 standard). In the U.S., after National Biodiesel Board was founded in 1992, the Congress and EPA approved BD20 as a fuel for diesel engine vehicles in 1998, and President Bush declared the expansion of new recycled energy including biodiesel in 2001. According to the active announcement of the government, the supply of biodiesel is increasing every year, and biodiesel is used in official vehicles of state governments and buses in addition to the U.S. Army, the U.S. Air Force, the Department of Energy and NASA. In Korea, based on the announcement regarding a model supply project for biodiesel by MOCCC in May, 2002, the government performed the project for two years, and now is investigating market reaction to and problems with biodiesel. The major advantage of biodiesel is a reduction of smoke emitted from vehicles. Although biodiesel also emits the greenhouse gas CO2, when viewed from an overall cycle of the process (from production to consumption) it yields very low amounts of CO2, and emits relatively low amounts of sulfur oxide (Sox) and particulate matters (PMs). Biodiesel made from vegetable resources may be self-produced domestically, which is an advantage for energy security, and may reduce environmental pollution by recycling waste resources, such as waste cooking oil. Also, in the aspect of infrastructure, diesel engine or gas station networks may be used, and thus less additional cost is required. However, although such advantages can be expected, biodiesel has several problems in substituting for conventional gasoline and volatile oils. Although biodiesel has to be mixed in a high ratio to reduce toxic chemicals in exhaust gases from vehicles, it may break down engines due to corrosion, and become denatured in long-term storage.
  • For these reasons, high purity products are required for methyl esters made from vegetable oil to be used as fuel oils for vehicles, and thus a separate vacuum distillation process is performed after the reaction of methyl esters. The vacuum distillation is performed at 2 to 3 torrs and a maximum temperature of 240□. After the vacuum distillation process, the distilled result is used as biodiesel fuel oil, and a distillation residue of about 10% is scrapped. Such a distillation residue generated in the production of biodiesel is a reactant of the vegetable oil with a structure of ester, and may be used as environmentally friendly lubricating base oil.
  • SUMMARY OF THE INVENTION
  • An embodiment of the invention provides a composition of a water-soluble metalworking fluid which uses a distillation residue generated in production of biodiesel as lubricating oil, and is mixed with other additives. The additives include a surfactant, a lubricating additive, a metal corrosion inhibitor, a rust inhibitor, a pH booster, a defoamer, a preservative, a pigment, etc., of which all are less harmful to the environment, and do not include any one of components which have use restrictions, such as nitrite, formaldehyde, boron and derivatives thereof, and an extreme pressure agent.
  • In one aspect, the present invention is directed to a composition of a water-soluble metalworking fluid produced by adding 5 to 70 wt % of additives to 20 to 95 wt % of distillation residues that is generated in production of biodiesel and used as lubricating base oil, and 0 to 40 wt % of ion exchange water. The distillation residue of the biodiesel is generated from canola oil, soybean oil, palm oil or jatropha oil.
  • The additive used in the present invention is at least one selected from the group consisting of a surfactant, a lubricating additive, a metal corrosion inhibitor, a rust inhibitor, a pH booster, a defoamer and a preservative. The surfactant used in the present invention is selected from ethoxide of lauryl alcohol or oleyl alcohol, ethoxide of castor oil, ethoxide of laurylamine or oleylamine, amine salt of oleic acid, amine salt of tall oil, amine salt of erucic acid, sulfonate, Hypermer A 70, Targat V 20, Veg Ester GY-112, Addconate H, Addconate M, succinic acid derivatives, amine salt of succinic acid and PEG-fatty acid ester. The lubricating base oil used in the present invention is at least one selected from the group consisting of petroleum-based hydrocarbon, vegetable oil and synthetic ester. Here, the petroleum-based hydrocarbon is a distilled mineral oil and has a kinematic viscosity of about 5 to 1000 cSt at 40□, and the vegetable oil and the synthetic ester are soybean oil, canola oil, sunflower oil, jatropha oil, palm oil, neopentyl glycol dioleate, trimethylolpropane trioleate, pentaerythritol tetraoleate, propylene glycol dioleate, ricinoleic acid condensate, or methyl ester of soybean oil, canola oil, jatropha oil or palm oil. The pH booster used in the present invention includes monoethanolamine, diethanolamine, triethanolamine, monoisopropanolamine, diisopropanolamine, triisopropanolamine, aminomethyl propanol or diglycolamine. The metal corrosion inhibitor used in the present invention includes benzotriazol, tolytriazol or derivatives thereof The rust inhibitor used in the present invention includes sebacic acid, Corfree M1, Irgacor 190 plus or derivatives thereof The defoamer used in the present invention includes polydimethyl siloxane, denatured polydimethyl siloxane, organic silicon derivatives or a silicon-based defoamer of silica. The preservative used in the present invention includes thiazoline, pyridine, morpholine, phenol, a nitro- or IPBC-based preservative.
  • DETAILED DESCRIPTION OF THE INVENTION Exemplary Embodiment 1
  • Water-soluble metalworking fluids were manufactured from a distillation residue generated in production of biodiesel, ion exchange water, a lubricating additive 1 (soybean oil, canola oil, palm oil, trimethylolpropane trioleate, pentaerythritol tetraoleate, or ricinoleic acid condensate), a surfactant, a metal corrosion inhibitor, a rust inhibitor, a pH booster, a defoamer and a preservative.
  • Contents of the water and the biodiesel distillation residue depend on application ranges of the product. As the product has a higher content of water, the diluted solution is clearer, while as the product has a higher content of the distillation residue, the diluted solution is milky white and has better lubrication performance.
  • TABLE 1
    Composition of Water-soluble Metalworking Fluid
    Name S-1 S-2 S-3 S-4 S-5
    Biodiesel distillation residue 51.3 67.8 37.3 61.0 91.0
    Ion exchange water 17.5 5.0 28.0 9.0 0
    Lubricating additive 1 4.5 1.5 6.0 3.5 0.7
    Surfactant 15.0 15.6 17.0 16.3 6.3
    pH booster 8.0 6.5 8.0 5.5 1.5
    Metal corrosion inhibitor 0.5 0.2 0.5 0.5
    Rust inhibitor 2.0 2.2 2.0 3.0 0.5
    Preservative 1.0 1.0 1.0 1.0
    Defoamer 0.2 0.2 0.2 0.2
  • Exemplary Embodiment 2
  • Water-soluble metalworking fluids were produced from a distillation residue generated in production of biodiesel, a lubricating additive 2 (petroleum-based hydrocarbon, methyl ester of soybean oil or canola oil, soybean oil, canola oil, or palm oil), a surfactant, a metal corrosion inhibitor, a rust inhibitor, a pH booster, a defoamer and a preservative.
  • TABLE 2
    Composition of Water-soluble Metalworking Fluid
    Name S-6 S-7 S-8 S-9 S-10
    Biodiesel distillation residue 43.0 44.8 25.3 40.8 52.0
    Ion exchange water 13.6 10.0 28.5 16.5 0
    Lubricating additive 2 18.0 19.5 18.3 12.0 16.0
    Surfactant 15.8 15.6 15.7 15.5 20.3
    pH booster 6.5 6.5 8.0 11.5 9.0
    Metal corrosion inhibitor 0.3 0.2 0.5 0.5 0.1
    Rust inhibitor 2.2 2.2 2.0 2.0 2.0
    Preservative 0.5 1.0 1.5 1.0 0.5
    Defoamer 0.1 0.2 0.2 0.2 0.1
  • Exemplary Embodiment 3
  • Water-soluble metalworking fluids were produced from a distillation residue generated in production of biodiesel, a lubricating additive 3 (petroleum-based hydrocarbon, methyl ester of soybean oil, canola oil or palm oil, trimethylolpropane trioleate, pentaerythritol tetraoleate or ricinoleic acid condensate), a surfactant, a metal corrosion inhibitor, a rust inhibitor, a pH booster, a defoamer and a preservative.
  • TABLE 3
    Composition of Water-soluble Metalworking Fluid
    Name S-11 S-12 S-13 S-14 S-15
    Biodiesel distillation residue 23.0 56.8 25.3 39.8 50.0
    Ion exchange water 18.6 10.0 32.0 17.5 5.0
    Lubricating additive 3 30.8 7.0 14.1 15.0 16.0
    Surfactant 16.9 15.2 13.9 13.5 16.3
    pH booster 6.5 7.0 10.5 10.5 9.0
    Metal corrosion inhibitor 0.3 0.3 0.5 0.5 0.5
    Rust inhibitor 2.2 2.5 2.0 2.0 2.0
    Preservative 1.5 1.0 1.5 1.0 1.0
    Defoamer 0.2 0.2 0.2 0.2 0.2
  • Exemplary Embodiment 4
  • Water-soluble metalworking fluids were produced from a distillation residue generated in production of biodiesel, a lubricating additive 4 (methyl ester of soybean oil, canola oil, jatropha oil or palm oil, soybean oil, canola oil, palm oil, jatropha oil or sunflower oil), a surfactant, a metal corrosion inhibitor, a rust inhibitor, a pH booster, a defoamer and a preservative.
  • TABLE 4
    Composition of Water-soluble Metalworking Fluid
    Name S-16 S-17 S-18 S-19 S-20
    Biodiesel distillation residue 62.3 57.7 42.9 40.0 67.3
    Ion exchange water 10.0 10.0 18.0 24.0 0
    Lubricating additive 4 4.0 2.5 6.0 5.0 4.0
    Surfactant 15.0 16.4 15.7 13.0 20.0
    pH booster 6.0 10.0 14.0 14.6 6.0
    Metal corrosion inhibitor 0.1 0.2 0.2 0.2 0.1
    Rust inhibitor 2.0 2.0 2.0 2.0 2.0
    Preservative 0.5 1.0 1.0 1.0 0.5
    Defoamer 0.1 0.2 0.2 0.2 0.1
  • EXAMPLE 1
  • TABLE 5
    Characteristics of Water-soluble Metalworking Fluid
    Item S-1 S-2 S-3 S-4 S-5
    Color/ Crude Dark Brown Dark Brown Brown Dark Brown Dark Brown
    Clearness Liquid Translucent Translucent Translucent Translucent Translucent
    Diluted White White White White White
    Liquid opaque opaque opaque opaque opaque
    pH (10%) 9.8 9.5 9.7 9.5 9.1
    Rust Inhibition 24 hrs 24 hrs 24 hrs 24 hrs 24 hrs
    (brix 3%) No rust No rust No rust No rust No rust
    Nonferrous Al None None None None None
    Metal
    discoloration Cu None None None None None
    Test (3%)
  • EXAMPLE 2
  • TABLE 6
    Characteristics of Water-soluble Metalworking Fluid
    Item S-6 S-7 S-8 S-9 S-10
    Color/ Crude Dark Brown Dark Brown Brown Dark Brown Dark Brown
    Clearness Liquid Translucent Translucent Translucent Translucent Translucent
    Diluted White White White White White
    Liquid opaque opaque opaque opaque opaque
    pH (10%) 9.5 9.6 9.5 9.8 9.7
    Rust Inhibition 24 hrs 24 hrs 24 hrs 24 hrs 24 hrs
    (brix 3%) No rust No rust No rust No rust No rust
    Nonferrous Al None None None None None
    Metal
    discoloration Cu None None None None None
    Test (3%)
  • EXAMPLE 3
  • TABLE 7
    Characteristics of Water-soluble Metalworking Fluid
    Item S-11 S-12 S-13 S-14 S-15
    Color/ Crude Dark Brown Dark Brown Brown Dark Brown Dark Brown
    Clearness Liquid Translucent Translucent Translucent Translucent Translucent
    Diluted White White White White White
    Liquid opaque opaque opaque opaque opaque
    pH (10%) 9.4 9.5 9.8 9.8 9.7
    Rust Inhibition 24 hrs 24 hrs 24 hrs 24 hrs 24 hrs
    (brix 3%) No rust No rust No rust No rust No rust
    Nonferrous Al None None None None None
    Metal
    Metal Cu None None None None None
    discoloration
    Test (3%)
  • EXAMPLE 4
  • TABLE 8
    Characteristics of Water-soluble Metalworking Fluid
    Item S-16 S-17 S-18 S-19 S-20
    Color/ Crude Dark Brown Dark Brown Dark Brown Dark Brown Dark Brown
    Clearness Liquid Translucent Translucent Translucent Translucent Translucent
    Diluted White White White White White
    Liquid opaque opaque opaque opaque opaque
    PH (10%) 9.6 9.6 9.7 9.7 9.4
    Rust Inhibition 24 hrs 24 hrs 24 hrs 24 hrs 24 hrs
    (brix 3%) No rust No rust No rust No rust No rust
    Nonferrous Al None None None None None
    Metal
    discoloration Cu None None None None None
    Test (3%)
  • A composition of a water-soluble metalworking fluid, using a biodiesel distillation residue that can be used as environmentally acceptable lubricating base oil, has good biodegradation, excellent lubrication and less toxicity bionomically. The water-soluble metalworking fluid may be very useful in business and recycling resources.
  • Exemplary embodiments of the present invention have been disclosed herein and, although specific terms are employed, they are used and are to be interpreted in a generic and descriptive sense only and not for purposes of limitation. Accordingly, it will be understood by those of ordinary skill in the art that various changes in form and details may be made without departing from the spirit and scope of the present invention as set forth in the following claims.

Claims (5)

1. A composition of a water-soluble metalworking fluid comprises 5 to 70 wt % of additive added to 95 wt % of distillation residue that is generated in production of biodiesel and used as lubricating base oil, and 0 to 40 wt % of ion exchange water.
2. The composition according to claim 1, wherein the distillation residue of the biodiesel is produced from canola oil, soybean oil, palm oil or jatropha oil.
3. The composition according to claim 1, wherein the additive comprises one or more selected from the group consisting of petroleum-based hydrocarbon, vegetable oil and synthetic ester.
4. The composition according to claim 3, wherein the petroleum-based hydrocarbon is a refined mineral oil, and has a kinematic viscosity of 5 to 1000 cSt at 40□.
5. The composition according to claim 3, wherein the vegetable oil and the synthetic ester comprise:
a lubricating additive selected from the group consisting of soybean oil, canola oil, sunflower oil, jatropha oil, palm oil, neopentyl glycol dioleate, trimethylolpropane trioleate, pentaerythritol tetraoleate, propylene glycol dioleate, ricinoleic acid condensate, and methyl ester of soybean oil, canola oil, jatropha oil or palm oil;
a surfactant selected from the group consisting of ethoxide of lauryl alcohol or oleyl alcohol, ethoxide of castor oil, ethoxide of laurylamine or oleylamine, amine salt of oleic acid, amine salt of tall oil, amine salt of erucic acid, sulfonate, Hypermer A 70, Targat V 20, Veg Ester GY-112, Addconate H, Addconate M, succinic acid derivatives, amine salt of succinic acid and PEG-fatty acid ester;
a pH booster selected from the group consisting of monoethanolamine, diethanolamine, triethanolamine, monoisopropanolamine, diisopropanolamine, triisopropanolamine, aminomethyl propanol and diglycolamine;
a metal corrosion inhibitor selected from the group consisting of benzotriazol, tolytriazol and derivatives thereof;
a rust inhibitor selected from the group consisting of sebacic acid, Corfree M1, Irgacor 190 plus and derivatives thereof;
a defoamer selected from the group consisting of polydimethyl siloxane, denatured polydimethyl siloxane, organic silicon derivatives and a silicon-based defoamer of silica; and
a preservative selected from the group consisting of thiazoline, pyridine, morpholine, phenol, nitro- and IPBC-based preservatives.
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Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20120245067A1 (en) * 2009-05-08 2012-09-27 Quaker Chemical Corporation Small particle size oil in water lubricant fluid
WO2013086483A1 (en) * 2011-12-09 2013-06-13 Evans Robert D Metalworking fluid composition and method for its use in the machining of compacted graphite iron
WO2014011838A1 (en) * 2012-07-11 2014-01-16 Lacerenza D Matthew Lubricating oil
US20140326117A1 (en) * 2011-11-17 2014-11-06 Idemitsu Kosan Co., Ltd. Water-soluble metalworking oil agent, metalworking fluid, and metalworking method
WO2013134358A3 (en) * 2012-03-07 2015-06-18 Quaker Chemical Corporation Cutting oil with vegetal oil
CN106479623A (en) * 2016-08-30 2017-03-08 宝捷润滑油镇江有限公司 The preparation method of the lubricating oil based on plant base artificial oil
US11396708B2 (en) * 2018-10-11 2022-07-26 Master Chemical Corporation Water soluble metalworking concentrate

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SG155077A1 (en) * 2008-02-21 2009-09-30 Cheng Kit Yew Composition and method of manufacture of biodiesel metalworking fluid
WO2010118891A1 (en) * 2009-04-17 2010-10-21 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Lubrication liquid and method for producing the same
DE102009026396A1 (en) * 2009-08-18 2011-04-07 Green Finance Ag Flux additive for bituminous compounds
KR101340007B1 (en) 2010-11-17 2013-12-10 (주) 토탈방재 Manufacturing method of emulsifier using by-product biodiesel
KR101750909B1 (en) * 2016-02-01 2017-07-11 ㈜ 바이오 루브 Water-soluble cutting oil comprising culture medium of photosynthetic bacteria

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3923702A (en) * 1974-08-08 1975-12-02 Emery Industries Inc Conversion of distillation residues to useful metal working lubricants
US20060042158A1 (en) * 2004-08-26 2006-03-02 Lee John H Fuel products from plant or animal lipids
US20060172897A1 (en) * 2005-02-02 2006-08-03 Osamu Yamamoto Process for machining metal and high performance aqueous lubricant therefor
US20070254820A1 (en) * 2006-04-28 2007-11-01 Tze-Chi Jao Diblock monopolymers as lubricant additives and lubricant formulations containing same
US20070277429A1 (en) * 2003-01-27 2007-12-06 Jackam John P Production of biodiesel and glycerin from high free fatty acid feedstocks
US20080085846A1 (en) * 2006-05-24 2008-04-10 Tran Bo L Hydraulic fluids and fire-resistant fluids comprising glycerin containing by-products

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1093959A (en) * 1966-06-20 1967-12-06 Henry W Peabody Ind Ltd Cold rolling lubrication
CH654020A5 (en) * 1982-07-19 1986-01-31 Sp K Byuro Analit Priborostr Lubricant for cold-forming of metals
DE3622826A1 (en) * 1986-07-08 1988-01-21 Henkel Kgaa POWDERED LUBRICANT ADDITIVES FOR WATER-BASED DRILL RINSING
AU626014B2 (en) * 1988-10-21 1992-07-23 Malaysian Palm Oil Board Production of alkyl esters from oils and fats
JP2955894B2 (en) * 1991-07-05 1999-10-04 ミヨシ油脂株式会社 Metal working oil
US6051538A (en) * 1999-01-26 2000-04-18 The Procter & Gamble Company Pour point depression of heavy cut methyl esters via alkyl methacrylate copolymer
KR20010045991A (en) * 1999-11-09 2001-06-05 이태구 Fuel oil composition including waste edible oil
JP2002265986A (en) * 2001-03-15 2002-09-18 Akio Kobayashi Method for producing fatty acid alkyl ester and glycerin
MXPA04001356A (en) * 2001-08-14 2004-10-27 United Soybean Board Soy-based methyl ester high performance metal working fluids.

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3923702A (en) * 1974-08-08 1975-12-02 Emery Industries Inc Conversion of distillation residues to useful metal working lubricants
US20070277429A1 (en) * 2003-01-27 2007-12-06 Jackam John P Production of biodiesel and glycerin from high free fatty acid feedstocks
US20060042158A1 (en) * 2004-08-26 2006-03-02 Lee John H Fuel products from plant or animal lipids
US20060172897A1 (en) * 2005-02-02 2006-08-03 Osamu Yamamoto Process for machining metal and high performance aqueous lubricant therefor
US20070254820A1 (en) * 2006-04-28 2007-11-01 Tze-Chi Jao Diblock monopolymers as lubricant additives and lubricant formulations containing same
US20080085846A1 (en) * 2006-05-24 2008-04-10 Tran Bo L Hydraulic fluids and fire-resistant fluids comprising glycerin containing by-products

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20120245067A1 (en) * 2009-05-08 2012-09-27 Quaker Chemical Corporation Small particle size oil in water lubricant fluid
US9707605B2 (en) * 2009-05-08 2017-07-18 Quaker Chemical Corporation Small particle size oil in water lubricant fluid
US20140326117A1 (en) * 2011-11-17 2014-11-06 Idemitsu Kosan Co., Ltd. Water-soluble metalworking oil agent, metalworking fluid, and metalworking method
US9683189B2 (en) * 2011-11-17 2017-06-20 Idemitsu Kosan Co., Ltd. Water-soluble metalworking oil agent, metalworking fluid, and metalworking method
WO2013086483A1 (en) * 2011-12-09 2013-06-13 Evans Robert D Metalworking fluid composition and method for its use in the machining of compacted graphite iron
WO2013134358A3 (en) * 2012-03-07 2015-06-18 Quaker Chemical Corporation Cutting oil with vegetal oil
WO2014011838A1 (en) * 2012-07-11 2014-01-16 Lacerenza D Matthew Lubricating oil
CN106479623A (en) * 2016-08-30 2017-03-08 宝捷润滑油镇江有限公司 The preparation method of the lubricating oil based on plant base artificial oil
US11396708B2 (en) * 2018-10-11 2022-07-26 Master Chemical Corporation Water soluble metalworking concentrate

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DE602007005212D1 (en) 2010-04-22

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