CN116590075A - Cutting fluid with high lubricity - Google Patents

Cutting fluid with high lubricity Download PDF

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Publication number
CN116590075A
CN116590075A CN202310435935.1A CN202310435935A CN116590075A CN 116590075 A CN116590075 A CN 116590075A CN 202310435935 A CN202310435935 A CN 202310435935A CN 116590075 A CN116590075 A CN 116590075A
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cutting fluid
oil
mixed solution
molybdenum sulfide
cage
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CN116590075B (en
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王克彬
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Ningbo Baorun Technology Co ltd
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Ningbo Baorun Technology Co ltd
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    • 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
    • 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
    • C10M169/045Mixtures of base-materials and additives the additives being a mixture of compounds of unknown or incompletely defined constitution and non-macromolecular compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/06Metal compounds
    • C10M2201/065Sulfides; Selenides; Tellurides
    • C10M2201/066Molybdenum sulfide
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/10Petroleum or coal fractions, e.g. tars, solvents, bitumen
    • C10M2203/1006Petroleum or coal fractions, e.g. tars, solvents, bitumen used as base material
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02Hydroxy compounds
    • C10M2207/023Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/026Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings with tertiary alkyl groups
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix 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
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/281Esters of (cyclo)aliphatic monocarboxylic acids
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/283Esters of polyhydroxy compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/40Fatty vegetable or animal oils
    • 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
    • C10M2207/40Fatty vegetable or animal oils
    • C10M2207/402Castor oils
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/22Heterocyclic nitrogen compounds
    • C10M2215/223Five-membered rings containing nitrogen and carbon only
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/06Oiliness; Film-strength; Anti-wear; Resistance to extreme pressure
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/10Inhibition of oxidation, e.g. anti-oxidants
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/20Metal working
    • C10N2040/22Metal working with essential removal of material, e.g. cutting, grinding or drilling
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P70/00Climate change mitigation technologies in the production process for final industrial or consumer products
    • Y02P70/10Greenhouse gas [GHG] capture, material saving, heat recovery or other energy efficient measures, e.g. motor control, characterised by manufacturing processes, e.g. for rolling metal or metal working

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

Abstract

In order to improve the lubricating property of the cutting fluid, the invention provides the cutting fluid with high lubricity, which comprises the following components in percentage by weight: 78-85% of base oil, 1-5% of molybdenum sulfide micron cage, 5-10% of animal and vegetable oil, 0.5-0.8% of antioxidant, 0.1-0.3% of antistatic agent and 5-9% of oily additive, wherein the total content of the components is 100%.

Description

Cutting fluid with high lubricity
Technical Field
The invention relates to the technical field of metal cutting processing.
Background
The cutting temperature in the metal cutting process is higher, the friction between the cutter and the metal workpiece is also larger, the cutter is easy to wear, and the workpiece is easy to thermally deform. The cutting fluid has the functions of cooling, lubricating, cleaning, rust prevention and the like, so that in the actual cutting process, the cutting fluid needs to be injected into a cutting machining area to reduce the temperature of the cutting machining area, reduce the friction between a cutter and a workpiece and the quality inspection of chips, clean chips generated by cutting, and inhibit the corrosion of the workpiece, the cutter, a machine tool, a clamp and the like caused by air, moisture, acid media and the like. In recent decades, along with the continuous improvement of cutting technology and continuous emergence of advanced cutting machine tools and continuous development of cutters and workpiece materials, the progress of cutting fluid technology is promoted. The consumption of the cutting fluid accounts for about 8% of the total consumption of the industrial lubricating oil. The traditional cutting fluid is divided into two major types of water-soluble cutting fluid and oil-soluble cutting fluid, the components of the cutting fluid mainly comprise base oil and additives, the formula is already mature after years of development, but with the development of a cutting process and the improvement of cutting equipment, particularly, the requirements on workpiece precision are continuously improved, and the water-soluble cutting fluid and the oil-soluble cutting fluid cannot completely meet the requirements of modern production, so that higher requirements are provided for the performances of the cutting fluid in the aspects of lubricating performance, heat exchange performance, permeability and the like.
Disclosure of Invention
In order to improve the lubricating property of the cutting fluid, the invention provides the cutting fluid with high lubricity, which comprises the following components in percentage by weight: 78-85% of base oil, 1-5% of molybdenum sulfide micron cage, 5-10% of animal and vegetable oil, 0.5-0.8% of antioxidant, 0.1-0.3% of antistatic agent and 5-9% of oily additive, wherein the total content of the components is 100%.
The molybdenum sulfide micro-cage is formed by assembling molybdenum sulfide particles, has a hollow spherical structure, has a porous surface, and contains stearic acid inside.
The molybdenum sulfide micro-cage diameter is about 1-3 microns.
The base oil is a low aromatic narrow fraction light mineral oil cut by distillation.
The animal and vegetable oil is one or more of pure rapeseed oil, epoxidized soybean oil, olive oil and de-esterified lard.
The antioxidant is di-tert-butyl-p-cresol (T501) and benzotriazole derivative (T551).
The oily additive synthesizes esters oil esters such as oleic acid esters, synthetic triol esters.
The preparation method of the high-lubrication cutting fluid comprises the following steps:
(1) The low aromatic hydrocarbon light mineral oil is distilled under reduced pressure, the head is pulled out, the light components are cut, and the flash point of the base oil is improved;
(2) Heating animal and vegetable oil to 65deg.C, slowly adding antioxidant to improve oxidation resistance of animal and vegetable oil, stirring to dissolve into uniform transparent, and maintaining at 60deg.C for 45-60 min;
(3) Adding molybdenum sulfide micro-cage into base oil, performing ultrasonic dispersion, adding the animal and vegetable oil, the antistatic agent and the oily additive obtained in the step (2), uniformly stirring at 65-70 ℃ to be transparent, and then continuously preserving heat and stirring for 45 minutes;
(4) Cooling the oil temperature to 45 ℃, and filtering the finished product.
The preparation method of the molybdenum sulfide micro-cage comprises the following steps: adding Cetyl Trimethyl Ammonium Bromide (CTAB) and stearic acid into a mixed solution of ethanol and water, and heating to fully dissolve the mixture to obtain a mixed solution A; dissolving ammonium dimolybdate in deionized water, adding thiourea, stirring until the ammonium dimolybdate is completely dissolved to obtain a mixed solution B, adding the mixed solution A into the mixed solution B, stirring and mixing uniformly to obtain a mixed solution C, pouring the mixed solution C into a hydrothermal kettle of a polytetrafluoroethylene inner container, performing hydrothermal reaction for 10-15h at 200-220 ℃, naturally cooling to room temperature, performing centrifugal separation, ultrasonically cleaning with deionized water and absolute ethyl alcohol for 3 times, and drying 8 h at 50-60 ℃ to obtain molybdenum sulfide micro cage particles.
Wherein, the mol ratio of ammonium dimolybdate to thiourea is 1:5-7, the mass concentration of CTAB in the mixed solution C is 0.1-0.5%, the mass concentration of stearic acid is 0.5-0.8%, the mass concentration of thiourea is 5-8%, and the volume ratio of ethanol to water is 1-2:1.
Advantageous effects
The molybdenum sulfide micro-cage is added into the cutting fluid and is assembled by molybdenum sulfide particles, the surface of the molybdenum sulfide micro-cage is of a hollow spherical structure, the surface of the molybdenum sulfide micro-cage is porous, stearic acid is contained in the molybdenum sulfide micro-cage, the spherical molybdenum sulfide micro-cage can play a role of a micro-steel ball at a friction interface in the cutting process, after the cutting process is stressed, the micro-cage is broken to generate nano-scale molybdenum sulfide particles, pits on the surface of a substrate are easy to fill, a compact lubrication protection film is formed, the spherical micro-cage and the spherical nano-particles can play a role of lubrication in a rolling friction mode, and when the molybdenum sulfide nano-particles are stressed further, friction between a cutter and a workpiece can be reduced in a sliding friction mode through the layered structure of the molybdenum sulfide. In addition, after the molybdenum sulfide micro-cage is crushed, stearic acid in the molybdenum sulfide micro-cage can be released, the stearic acid can be subjected to saponification reaction with the metal surface, an adsorption film is formed on the metal surface, the film forming capability of the cutting fluid is improved, and the lubricating performance of the cutting fluid is further improved.
Description of the embodiments
Examples
The high-lubricity cutting fluid comprises the following components in percentage by weight: 78% of base oil, 3% of molybdenum sulfide micro-cage, 10% of animal and vegetable oil, 0.7% of antioxidant, 0.3% of antistatic agent and 8% of oily additive.
The molybdenum sulfide micro-cage is formed by assembling molybdenum sulfide particles, has a hollow spherical structure, has a porous surface, and contains stearic acid inside.
The molybdenum sulfide micro-cage diameter is about 1 micron.
The base oil is a low aromatic narrow fraction light mineral oil cut by distillation.
The animal and vegetable oil is epoxidized soybean oil.
The antioxidant is di-tert-butyl-p-cresol (T501).
The oily additive is oleate.
The preparation method of the high-lubrication cutting fluid comprises the following steps:
(1) The low aromatic hydrocarbon light mineral oil is distilled under reduced pressure, the head is pulled out, the light components are cut, and the flash point of the base oil is improved;
(2) Heating animal and vegetable oil to 65deg.C, slowly adding antioxidant to improve oxidation resistance of animal and vegetable oil, stirring to dissolve into uniform transparent, and maintaining at 60deg.C for 45-60 min;
(3) Adding molybdenum sulfide micro-cage into base oil, performing ultrasonic dispersion, adding the animal and vegetable oil, the antistatic agent and the oily additive obtained in the step (2), uniformly stirring at 65-70 ℃ to be transparent, and then continuously preserving heat and stirring for 45 minutes;
(4) Cooling the oil temperature to 45 ℃, and filtering the finished product.
The preparation method of the molybdenum sulfide micro-cage comprises the following steps: adding Cetyl Trimethyl Ammonium Bromide (CTAB) and stearic acid into a mixed solution of ethanol and water, and heating to fully dissolve the mixture to obtain a mixed solution A; dissolving ammonium dimolybdate in deionized water, adding thiourea, stirring until the ammonium dimolybdate is completely dissolved to obtain a mixed solution B, adding the mixed solution A into the mixed solution B, stirring and mixing uniformly, pouring the mixed solution A into a hydrothermal kettle of a polytetrafluoroethylene inner container, carrying out hydrothermal reaction for 10 hours at 220 ℃, naturally cooling to room temperature, carrying out centrifugal separation, carrying out ultrasonic cleaning on the mixed solution with deionized water and absolute ethyl alcohol for 3 times, and drying 8 h at 50-60 ℃ to obtain molybdenum sulfide micro cage particles.
Wherein, the mol ratio of ammonium dimolybdate to thiourea is 1:5, the mass concentration of CTAB in the mixed solution C is 0.5%, the mass concentration of stearic acid is 0.8%, the mass concentration of thiourea is 8%, and the volume ratio of ethanol to water is 2:1.
Maximum seizure-free load 976P of the resulting highly lubricated cutting fluid B N (GB/T3142), the diameter of the mill marks is 0.311mm, and the lubricating performance is good.
Examples
The high-lubricity cutting fluid comprises the following components in percentage by weight: 85% of base oil, 1% of molybdenum sulfide micro-cage, 5% of animal and vegetable oil, 0.7% of antioxidant, 0.3% of antistatic agent and 8% of oily additive.
The molybdenum sulfide micro-cage is formed by assembling molybdenum sulfide particles, has a hollow spherical structure, has a porous surface, and contains stearic acid inside.
The base oil is a low aromatic narrow fraction light mineral oil cut by distillation.
The animal and vegetable oil is a mixture of epoxidized soybean oil and olive oil.
The antioxidant is a benzotriazole derivative (T551).
The oily additive is oleate.
The preparation method of the high-lubrication cutting fluid comprises the following steps:
(1) The low aromatic hydrocarbon light mineral oil is distilled under reduced pressure, the head is pulled out, the light components are cut, and the flash point of the base oil is improved;
(2) Heating animal and vegetable oil to 65deg.C, slowly adding antioxidant to improve oxidation resistance of animal and vegetable oil, stirring to dissolve into uniform transparent, and maintaining at 60deg.C for 45-60 min;
(3) Adding molybdenum sulfide micro-cage into base oil, performing ultrasonic dispersion, adding the animal and vegetable oil, the antistatic agent and the oily additive obtained in the step (2), uniformly stirring at 65-70 ℃ to be transparent, and then continuously preserving heat and stirring for 45 minutes;
(4) Cooling the oil temperature to 45 ℃, and filtering the finished product.
The preparation method of the molybdenum sulfide micro-cage comprises the following steps: adding Cetyl Trimethyl Ammonium Bromide (CTAB) and stearic acid into a mixed solution of ethanol and water, and heating to fully dissolve the mixture to obtain a mixed solution A; dissolving ammonium dimolybdate in deionized water, adding thiourea, stirring until the ammonium dimolybdate is completely dissolved to obtain a mixed solution B, adding the mixed solution A into the mixed solution B, stirring and mixing uniformly, pouring the mixed solution A into a hydrothermal kettle of a polytetrafluoroethylene inner container, carrying out hydrothermal reaction for 10 hours at 220 ℃, naturally cooling to room temperature, carrying out centrifugal separation, carrying out ultrasonic cleaning on the mixed solution with deionized water and absolute ethyl alcohol for 3 times, and drying 8 h at 50-60 ℃ to obtain molybdenum sulfide micro cage particles.
Wherein, the mol ratio of ammonium dimolybdate to thiourea is 1:7, the mass concentration of CTAB in the mixed solution C is 0.1%, the mass concentration of stearic acid is 0.5%, the mass concentration of thiourea is 5%, and the volume ratio of ethanol to water is 1:1.
Maximum seizure-free load 972P of the resulting highly lubricated cutting fluid B N (GB/T3142), the diameter of the mill marks is 0.315mm, and the lubricating performance is good.
Comparative example 1
The difference from example 1 is that no molybdenum sulfide micro-cage was added, and the maximum seizure free load 680 and P of the cutting fluid was obtained B N (GB/T3142), the diameter of the mill spot is 0.532mm.
Comparative example 2
The difference from example 1 is that the molybdenum sulfide micro-cage of the present invention was replaced with a molybdenum sulfide hollow sphere having a diameter of 1.5 μm (in which stearic acid was not contained), and the maximum bite-free load of the resulting cutting fluid was 810P B N (GB/T3142), plaque diameter 0.481mm.
Comparative example 3
The difference from example 1 is that molybdenum sulfide hollow spheres having a diameter of 1.5 μm (in which stearic acid is not contained) are used instead of the molybdenum sulfide micro-cage of the present invention, but in step (3) of preparing a cutting fluid, stearic acid is added to a base oil together with molybdenum sulfide hollow spheres, and dispersed by ultrasonic. Maximum bite-free load 832, 832P of the resulting cutting fluid B N (GB/T3142) with a mill spot diameter of 0.485mm, it has been found that the addition of molybdenum sulphide and stearic acid, respectively, does not significantly improve the lubricating properties of the cutting fluid.

Claims (9)

1. A high-lubricity cutting fluid is characterized in that: comprises the following components in percentage by weight: 78-85% of base oil, 1-5% of molybdenum sulfide micron cage, 5-10% of animal and vegetable oil, 0.5-0.8% of antioxidant, 0.1-0.3% of antistatic agent, 5-9% of oily additive and 100% of each component;
the molybdenum sulfide micro-cage is formed by assembling molybdenum sulfide particles, has a hollow spherical structure, has a porous surface, and contains stearic acid inside.
2. The cutting fluid of claim 1, wherein: the diameter of the molybdenum sulfide micron cage is 1-3 microns.
3. The cutting fluid of claim 1, wherein: the base oil is a low aromatic narrow fraction light mineral oil cut by distillation.
4. The cutting fluid of claim 1, wherein: the animal and vegetable oil is one or more of pure rapeseed oil, epoxidized soybean oil, olive oil and de-esterified lard.
5. The cutting fluid of claim 1, wherein: the antioxidant is di-tert-butyl-p-cresol (T501) or a benzotriazole derivative (T551).
6. The cutting fluid of claim 1, wherein: the oily additive is oleic acid ester or synthetic triol ester.
7. The method for preparing the cutting fluid according to claim 1, wherein: the method comprises the following steps:
(1) The low aromatic hydrocarbon light mineral oil is distilled under reduced pressure, the head is pulled out, the light components are cut, and the flash point of the base oil is improved;
(2) Heating animal and vegetable oil to 65deg.C, adding antioxidant to improve oxidation resistance of animal and vegetable oil, stirring to dissolve into uniform transparent, and maintaining at 60deg.C for 45-60 min;
(3) Adding molybdenum sulfide micro-cage into base oil, performing ultrasonic dispersion, adding the animal and vegetable oil, the antistatic agent and the oily additive obtained in the step (2), uniformly stirring at 65-70 ℃ to be transparent, and then continuously preserving heat and stirring for 45 minutes;
(4) Cooling the oil temperature to 45 ℃, and filtering the finished product.
8. The method of manufacturing according to claim 7, wherein:
the preparation method of the molybdenum sulfide micro-cage comprises the following steps: adding Cetyl Trimethyl Ammonium Bromide (CTAB) and stearic acid into a mixed solution of ethanol and water, and heating to fully dissolve the mixture to obtain a mixed solution A; dissolving ammonium dimolybdate in deionized water, adding thiourea, stirring until the ammonium dimolybdate is completely dissolved to obtain a mixed solution B, adding the mixed solution A into the mixed solution B, stirring and mixing uniformly to obtain a mixed solution C, pouring the mixed solution C into a hydrothermal kettle of a polytetrafluoroethylene inner container, performing hydrothermal reaction for 10-15h at 200-220 ℃, naturally cooling to room temperature, performing centrifugal separation, ultrasonically cleaning with deionized water and absolute ethyl alcohol for 3 times, and drying 8 h at 50-60 ℃ to obtain molybdenum sulfide micro cage particles.
9. The method of preparing as claimed in claim 8, wherein: the molar ratio of ammonium dimolybdate to thiourea is 1:5-7, the mass concentration of CTAB in the mixed solution C is 0.1-0.5%, the mass concentration of stearic acid is 0.5-0.8%, the mass concentration of thiourea is 5-8%, and the volume ratio of ethanol to water is 1-2:1.
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Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103602387A (en) * 2013-10-22 2014-02-26 青岛海伴塑胶工贸有限公司 Novel cooling cutting fluid
CN104357181A (en) * 2014-09-30 2015-02-18 宁波保润石化有限公司 Special magnetic cutting oil and preparation method thereof
US20170009171A1 (en) * 2015-07-07 2017-01-12 Nanotech Industrial Solutions, Inc. Industrial lubricant including metal chalcogenide particles and phosphorus-based additive
CN106803589A (en) * 2017-02-26 2017-06-06 桂林理工大学 A kind of single dispersing class flower ball-shaped MoS2Raw powder's production technology

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103602387A (en) * 2013-10-22 2014-02-26 青岛海伴塑胶工贸有限公司 Novel cooling cutting fluid
CN104357181A (en) * 2014-09-30 2015-02-18 宁波保润石化有限公司 Special magnetic cutting oil and preparation method thereof
US20170009171A1 (en) * 2015-07-07 2017-01-12 Nanotech Industrial Solutions, Inc. Industrial lubricant including metal chalcogenide particles and phosphorus-based additive
CN106803589A (en) * 2017-02-26 2017-06-06 桂林理工大学 A kind of single dispersing class flower ball-shaped MoS2Raw powder's production technology

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
霍英杰;侯锁霞;张好强;吴超;张舵;: "纳米二硫化钼的水热法可控制备及极压性能研究", 润滑与密封, no. 09, 15 September 2017 (2017-09-15), pages 107 - 110 *

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