JP2012197327A - Oil composition for trace oil feeding formula processing - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a metal processing oil composition that can achieve high level machining performance and is appropriate for a trace oil feeding type processing.SOLUTION: The trace oil feeding type processing oil composition includes: at least one base oil chosen from a mineral oil and a synthetic oil; and a compound having a perfluoroalkyl group. It becomes possible to improve the dischargeability of the oil, and to improve processing efficiency and tool life in metal workings of cutting, grinding, component rolling or the like according to the oil composition for the trace oil feeding type processing.

Description

  The present invention relates to an oil composition for processing with an extremely small amount of oil supply.

  Metal processing includes cutting, grinding, rolling, forging, pressing, drawing, rolling, etc. These processes are usually performed using a lubricant (hereinafter also simply referred to as an oil). Is called.

  For example, in cutting and grinding, productivity in machining, such as extending the life of tools such as drills, end mills, tools, and grindstones used in machining, improving the surface roughness of workpieces, and thereby improving machining efficiency For the purpose of improving the quality, oil for cutting and grinding is usually used.

  The cutting and grinding fluids are water-soluble cutting and grinding fluids that use diluted surfactant and lubricant components in water, and water-insoluble cutting and grinding fluids that use mineral oil as the main ingredient. There are roughly two types of processing oils. In the conventional cutting / grinding process, a relatively large amount of the cutting / grinding oil is supplied to the processing site regardless of which oil is used.

  The most basic and important functions of the oil for cutting and grinding are lubrication and cooling. In general, water-insoluble cutting and grinding fluids are excellent in lubrication performance, and water-soluble cutting and grinding fluids are excellent in cooling performance. The water-insoluble oil usually requires a large amount of water-insoluble cutting / grinding oil of several liters per minute to tens of liters in some cases.

  Cutting and grinding fluids effective for improving the processing efficiency are not preferable from another aspect, and a typical problem is the influence on the environment. Regardless of water-insolubility and water-solubility, oils gradually deteriorate during use and eventually become unusable. For example, in the case of a water-soluble oil agent, the stability of the liquid is reduced due to the generation of microorganisms, resulting in separation of components, or the sanitary environment is significantly reduced and its use is impossible. In the case of a water-insoluble oil agent, an acidic component generated by the progress of oxidation corrodes the metal material, or a significant change in viscosity occurs, making it impossible to use. Further, the oil agent may adhere to chips and be consumed, resulting in waste.

  In such a case, the deteriorated oil is discarded and a new oil is used. At this time, the oil discharged as waste requires various treatments so as not to affect the environment. For example, cutting and grinding fluids that have been developed with a priority on improving work efficiency often use chlorinated compounds that may generate toxic dioxins during incineration. Processing is required. For this reason, cutting and grinding fluids that do not contain chlorinated compounds have also been developed, but even with such cutting and grinding fluids that do not contain such harmful components, there is a problem of the environmental impact associated with the massive discharge of waste. is there. Further, in the case of water-soluble oils, there is a possibility of polluting the environmental water area, so it is necessary to perform advanced treatment at high cost.

  Recently, in order to deal with the above-mentioned problems, a study is being made to replace the cutting / grinding fluid by blowing cold air on the cutting / grinding portion and cooling it. On the other hand, it is impossible to obtain one of the properties required for lubrication.

  Under such a background, cutting while supplying an extremely small amount of oil agent of about 1 / 100,000 to 1 / 1000,000 in comparison with the amount of oil agent used in normal cutting / grinding work together with a compressed fluid (for example, compressed air).・ A very small amount of oil supply method for grinding and grinding has been developed. In this system, the cooling effect by compressed air can be obtained, and the amount of waste can be reduced because a very small amount of oil is used, so that the environmental impact caused by the large amount of waste can also be improved ( For example, see Patent Document 1).

  Even in such ultra-trace oil supply method cutting / grinding method, conventionally, synthetic oils such as mineral oil and ester are used as base oils, and oil-based agents and extreme pressure agents are added as necessary to improve processing efficiency. Agents have been used. In particular, oily agents such as alcohols, carboxylic acids, sulfides of unsaturated carboxylic acids, polyoxyalkylene compounds, esters, hydrocarbyl ethers of polyhydric alcohols, amines, etc. are used. It is used by adding 15% by mass (for example, see Patent Document 2).

  On the other hand, when processing aluminum, the water supply agent containing water may be used because the cooling performance is insufficient in the ultra-trace oil supply method.

International Publication No. 02/081605 Pamphlet JP 2006-249369 A

  The very small amount of oil supply system is characterized by a small amount of oil supplied to the workpiece, but especially when using a system with a hole for supplying oil called a center-through, a hole with a very small inner diameter. The oil passes through. Therefore, the supply of the oil agent is often unstable, which may cause defective products when continuously processing.

  This tendency of oil discharge failure is more likely to occur in water systems that have higher surface tension than non-water systems, and this is one of the factors that hinder the spread of ultra-trace oil supply processing in aluminum, which often uses water-based oils. ing.

  The present invention has been made in view of such circumstances, and an object of the present invention is to provide a metal working oil composition that is capable of achieving a high level of processing performance and that is suitable for processing with an extremely small amount of oil supply system. And

  As a result of intensive studies to achieve the above object, the present inventors have found that the above problems can be solved by using a specific oil, and have completed the present invention.

  That is, this invention provides the trace amount oil supply type | formula oil composition for processing containing at least 1 sort (s) of base oil chosen from mineral oil and synthetic oil, and the compound which has a perfluoroalkyl group.

  The perfluoroalkyl group is preferably at least one selected from a perfluoroalkyl sulfonate group, a perfluoroalkylcarbonyl group, and a perfluorosulfonamide group.

［式（１）中、Ｒ^１は炭素数１〜１２のアルキル基又は炭素数２〜１２のアルケニル基を示し、Ａは炭素数１〜１８のパーフルオロアルキル基を示し、Ｂは水素原子、炭素数１〜１２のアルキル基、炭素数２〜１２のアルケニル基、炭素数１〜１２のアルカノール基、炭素数６〜１２のアリール基、又は一般式（２）：

（式（２）中、Ｒ^２は水素原子、炭素数１〜１８のアルキル基、炭素数２〜１８のアルケニル基又は炭素数６〜１８のアリール基を示し、Ｒ^３は炭素数１〜１２のアルキレン基又は炭素数２〜１２のアルケニレン基を示す。）
で示される基を示す。］ It is preferable that the trace amount oil agent supply type processing oil agent composition of the present invention contains a compound having a structure represented by the following general formula (1) as a compound having a perfluoroalkyl group.

[In the formula (1), R ¹ represents an alkyl group having 1 to 12 carbon atoms or an alkenyl group having 2 to 12 carbon atoms, A represents a perfluoroalkyl group having 1 to 18 carbon atoms, B represents a hydrogen atom, A C1-C12 alkyl group, a C2-C12 alkenyl group, a C1-C12 alkanol group, a C6-C12 aryl group, or General formula (2):

(In the formula (2), ^{R 2} represents a hydrogen atom, an alkyl group having 1 to 18 carbon atoms, an alkenyl group or an aryl group having 6 to 18 carbon atoms having 2 to 18 carbon atoms, ^{R 3} is 1 to 12 carbon atoms An alkylene group or an alkenylene group having 2 to 12 carbon atoms.)
The group shown by is shown. ]

  According to the oil composition for processing with a very small amount of oil supply of the present invention, in metal processing such as cutting, grinding, and rolling, it is possible to improve the discharge of oil and improve the processing efficiency and tool life. It becomes possible.

  Hereinafter, preferred embodiments of the present invention will be described in detail.

  An oil composition for processing with an extremely small amount of oil according to this embodiment (hereinafter also referred to as “an oil composition according to this embodiment” in some cases) includes at least one base oil selected from mineral oil and synthetic oil. And a compound having a perfluoroalkyl group.

  As long as the base oil does not impair the processing efficiency, the tool life, and the handleability, any base oil that is used in ordinary lubricating oils can be mixed and used. Such base oil may be either mineral oil or synthetic oil, or a mixture thereof.

  As mineral oil, for example, a lubricating oil fraction obtained by subjecting crude oil to atmospheric distillation and vacuum distillation is subjected to solvent removal, solvent extraction, hydrocracking, solvent dewaxing, catalytic dewaxing, catalytic dewaxing, hydrogenation. Examples thereof include paraffinic mineral oil or naphthenic mineral oil that is refined by appropriately combining one or more purification treatments such as purification, sulfuric acid washing, and clay treatment.

  Specific examples of the synthetic oil include propylene oligomer, polybutene, polyisobutylene, 1-octene oligomer, 1-decene oligomer, ethylene and propylene co-oligomer, ethylene and 1-octene co-oligomer, ethylene and 1- Poly α-olefins such as co-oligomers with decene or their hydrides; isoparaffins; alkylbenzenes such as monoalkylbenzenes, dialkylbenzenes and polyalkylbenzenes; alkylnaphthalenes such as monoalkylnaphthalenes, dialkylnaphthalenes and polyalkylnaphthalenes; dioctyl adipates, di Dibasic acid esters such as 2-ethylhexyl adipate, diisodecyl adipate, ditridecyl adipate, di-2-ethylhexyl sebacate, ditridecyl glutarate; Tribasic acid esters such as tutonic acid; polyol esters such as trimethylolpropane caprylate, trimethylolpropane pelargonate, trimethylolpropane oleate, pentaerythritol 2-ethylhexanoate, pentaerythritol pelargonate; polyethylene glycol, polypropylene glycol Polyglycols such as polyoxyethyleneoxypropylene glycol, polyethylene glycol monoether, polypropylene glycol monoether, polyoxyethyleneoxypropylene glycol monoether, polyethylene glycol diether, polypropylene glycol diether, polyoxyethyleneoxypropylene glycol diether; Monoalkyl diphenyl ether, dialkyl diphenyl ether , Monoalkyl triphenyl ether, dialkyl triphenyl ether, tetraphenyl ether, monoalkyl tetraphenyl ether, dialkyl tetraphenyl ether, phenyl ether such as pentaphenyl ether; silicone oil; fluoro ether such as perfluoro ether, etc. These can be used alone or in combination of two or more.

  Among the above base oils, a polyol ester is more preferable from the viewpoint of further improving the handleability.

  In the compound having a perfluoroalkyl group used in the present embodiment, the perfluoroalkyl group may be linear or branched, but is preferably linear, saturated or unsaturated, and has 1 to 18 carbon atoms, preferably 1 It is 12 or less, more preferably 1 or more and 6 or less, and most preferably 1 or more and 4 or less. When the number of carbon atoms is 19 or more, it is inferior in decomposability and may be an environmental burden when released to the outside.

  Examples of the compound having a perfluoroalkyl group include perfluoroalkylsulfonamide, perfluoroalkyl alkylene oxide adduct, perfluoroalkylamine, perfluoroalkylsulfonic acid, perfluoroalkylcarboxylic acid, and salts and derivatives thereof. It is done.

［式（１）中、Ｒ^１は炭素数１〜１２のアルキル基又は炭素数２〜１２のアルケニル基を示し、Ａは炭素数１〜１８のパーフルオロアルキル基を示し、Ｂは水素原子、炭素数１〜１８のアルキル基、炭素数２〜１８のアルケニル基、炭素数１〜１８のアルカノール基、炭素数６〜１８のアリール基、又は一般式（２）：

（式（２）中、Ｒ^２は水素原子、炭素数１〜１８のアルキル基、炭素数２〜１８のアルケニル基又は炭素数６〜１８のアリール基を示し、Ｒ^３は炭素数１〜１２のアルキレン基又は炭素数２〜１２のアルケニレン基を示す。）
で示される基を示す。］ As the perfluoroalkylsulfonamide, a compound having a structure represented by the following general formula (1) is preferable.

[In the formula (1), R ¹ represents an alkyl group having 1 to 12 carbon atoms or an alkenyl group having 2 to 12 carbon atoms, A represents a perfluoroalkyl group having 1 to 18 carbon atoms, B represents a hydrogen atom, C1-C18 alkyl group, C2-C18 alkenyl group, C1-C18 alkanol group, C6-C18 aryl group, or General formula (2):

(In the formula (2), ^{R 2} represents a hydrogen atom, an alkyl group having 1 to 18 carbon atoms, an alkenyl group or an aryl group having 6 to 18 carbon atoms having 2 to 18 carbon atoms, ^{R 3} is 1 to 12 carbon atoms An alkylene group or an alkenylene group having 2 to 12 carbon atoms.)
The group shown by is shown. ]

A may be linear or branched, but is preferably linear. A may be saturated or unsaturated, but is preferably saturated. The carbon number of A is 1 or more and 18 or less, preferably 1 or more and 12 or less, more preferably 1 or more and 6 or less, and most preferably 1 or more and 4 or less. When the number of carbon atoms is 19 or more, it is inferior in decomposability and may be an environmental burden when released to the outside. The carbon number of B is preferably 2-12, more preferably 3-8, and most preferably 4-6. B may be linear or branched, and may be saturated or unsaturated. R ¹ is preferably an alkyl group having 1 to 8 carbon atoms, more preferably 1 to 6, most preferably 1 to 4, and may be linear or branched, and may be saturated or unsaturated. R ² is preferably an alkyl group or alkenyl group having 6 to 18 carbon atoms, more preferably an alkyl group or alkenyl group having 8 to 18 carbon atoms, and most preferably an alkyl group or alkenyl group having 12 to 18 carbon atoms. preferable. The alkyl group or alkenyl group may be linear or branched, but is preferably branched. When used as a working fluid composition, an alkyl group having 1 to 6 carbon atoms and an alkenyl group having 2 to 6 carbon atoms are preferable, an alkyl group having 1 to 4 carbon atoms and an alkenyl group having 2 to 4 carbon atoms are more preferable, Most preferred is an alkenyl group of 3. The alkyl group and alkenyl group may be linear or branched, and may be saturated or unsaturated. R ³ is preferably an alkylene group having 1 to 8 carbon atoms or an alkenylene group having 2 to 8 carbon atoms, and preferably an alkylene group having 1 to 4 carbon atoms.

  The perfluoroalkylsulfonamide may be a primary amide, a secondary amide, or a tertiary amide, but a tertiary amide is preferred.

As the alkylene oxide adduct of perfluoroalkyl, a compound represented by the following general formula (3) is suitable. Examples of the alkylene oxide include ethylene oxide, propylene oxide, and butylene oxide, and ethylene oxide and propylene oxide are preferable. The added mole number of alkylene oxide is 1 or more and 20 or less, preferably 1 or more and 12 or less, more preferably 1 or more and 8 or less, and most preferably 1 or more and 6 or less. It may be an adduct of a single alkylene oxide or an adduct in which a plurality of alkylene oxides are mixed. In this case, the alkylene oxide polymerization portion may be a block polymer or a random polymer, but a random polymer is preferred.
_{^{R 4 -O- (R 5 O)}} a -A (3)
Wherein (3), A represents a perfluoroalkyl of 1 to 18 carbon atoms, ^{R 4} represents a hydrogen atom, an alkyl group or an acyl group having 1 to 12 carbon atoms having 1 to 12 carbon atoms, ^{R 5} is A C2-C4 alkylene group is shown, a shows the integer of 1-20. ]

As the perfluoroalkylamine, a compound represented by the following general formula (4) is suitable. The number of perfluoroalkyl groups bonded to nitrogen may be 1 to 3, but is preferably one. Moreover, although 3-b R < ⁶ > couple | bonded with nitrogen may or may not contain a hydrogen atom, it is preferable that one is a hydrogen atom. Furthermore, R ⁶ other than a hydrogen atom that the compound may have is preferably an alkyl group or an alkanol group. The alkyl group and alkanol group represented by R ⁶ may be linear or branched, and may be saturated or unsaturated.
_{^{(R 6) (3-b}} ) -N-A b (4)
Wherein (4), A represents a perfluoroalkyl group having 1 to 18 carbon atoms, ^{R 6} is a hydrogen atom, an alkyl group having 1 to 18 carbon atoms, 6 to an alkanol group or a carbon number of 1 to 18 carbon atoms 12 represents an aryl group having 7 to 12 carbon atoms, a cycloalkyl group having 6 to 12 carbon atoms, or an alkylcycloalkyl group having 7 to 12 carbon atoms, and b represents an integer of 1 to 3. ]

  Perfluoroalkyl sulfonic acid is a sulfonic acid having a C 1-18 perfluoroalkyl group. Examples of the salt include alkali metal salts, alkaline earth metal salts, and amine salts. Sodium, potassium are used as the alkali metal, and magnesium, calcium, and barium are used as the alkaline earth. Of these, sodium and potassium are preferable. Examples of amines include monoamines, polyamines, and alkanolamines.

  Monoamines include alkylamines having 1 to 3 alkyl groups having 1 to 22 carbon atoms, alkenylamines having alkenyl groups having 2 to 23 carbon atoms, two methyl groups and one alkenyl group having 2 to 23 carbon atoms. A monoamine having an aromatic group, an aromatic substituted alkylamine, a cycloalkylamine having a cycloalkyl group having 5 to 16 carbon atoms, a monoamine having two methyl groups and a cycloalkyl group, a cycloalkyl group substituted by a methyl group and / or an ethyl group And alkylcycloalkylamine having the following formula. The monoamine here includes monoamines such as beef tallow amine derived from fats and oils.

  Examples of the polyamine include alkylene polyamines having 1 to 5 alkylene groups having 2 to 4 carbon atoms, N-alkylethylenediamine having an alkyl group having 1 to 23 carbon atoms, and N-alkenylethylenediamine having an alkenyl group having 2 to 23 carbon atoms. , N-alkyl or N-alkenylalkylene polyamines. The polyamine here includes polyamines derived from fats and oils (such as beef tallow polyamine).

  Examples of the alkanolamine include mono-, di- and trialkanolamines of alcohols having 1 to 16 carbon atoms.

  The sulfonic acid which comprises a sulfonate can use the well-known thing manufactured by the conventional method. Specifically, from sulfonated alkyl aromatic compounds in the lubricating oil fraction of mineral oil, petroleum sulfonic acids such as mahogany acid produced as a by-product during white oil production, or from alkylbenzene production plants used as raw materials for detergents, etc. Synthetic sulfones such as those obtained by alkylating the by-produced polyolefin to benzene, sulfonated alkylbenzenes having linear or branched alkyl groups, and sulfonated alkylnaphthalenes such as dinonylnaphthalene Acid etc. are mentioned.

  Perfluoroalkyl carboxylic acids are compounds in which a carboxyl group is bonded to a C 1-18 perfluoroalkyl group. Specific examples of the salt include the same salts as those of perfluorosulfonic acid.

  The content of the compound having a perfluoroalkyl group is preferably 0.001% by mass or more, more preferably 0.01% by mass or more, further preferably 0.05% by mass or more, based on the total amount of the oil composition. Most preferably, it is 0.1 mass% or more. The content is preferably 5% by mass or less, more preferably 3% by mass or less, still more preferably 2% by mass or less, and most preferably 1% by mass or less, based on the total amount of the oil composition. If the content exceeds 5% by mass, the coefficient of friction increases, which may adversely affect workability. Moreover, when the content is less than 0.001% by mass, it is difficult to obtain the effect.

［式（５）中、Ｒ^７は炭素数１〜３０の炭化水素基を表し、ｃは１〜６の整数を表し、ｄは０〜５の整数を表す。］

［式（６）中、Ｒ^８は炭素数１〜３０の炭化水素基を表し、ｅは１〜６の整数を表し、ｆは０〜５の整数を表す。］ The oil agent composition according to the present embodiment preferably contains (B) an oily agent from the viewpoint of improvement in processing efficiency and improvement in tool life. Examples of the oily agent include (B-1) alcohol (excluding (B-6) below), (B-2) carboxylic acid and its metal salt, (B-3) sulfide of unsaturated carboxylic acid, ( B-4) a compound represented by the following general formula (5), (B-5) a compound represented by the following general formula (6), (B-6) a polyoxyalkylene compound, (B-7) ester ( * However, base esters are excluded), (B-8) hydrocarbyl ethers of polyhydric alcohols, (B-9) amines, and the like.

Wherein (5), ^{R 7} represents a hydrocarbon group having 1 to 30 carbon atoms, c is an integer of 1 to 6, d is an integer of 0-5. ]

Wherein (6), ^{R 8} represents a hydrocarbon group having 1 to 30 carbon atoms, e represents an integer of 1 to 6, f represents an integer of 0 to 5. ]

  (B-1) As the monohydric alcohol, the alcohol is a linear alcohol having 3 to 18 carbon atoms, a branched alcohol having 3 to 18 carbon atoms, a cycloalkyl alcohol having 5 to 10 carbon atoms or an alkylcyclohexane. Examples include alkyl alcohols. Specifically, linear or branched propanol (including n-propanol, 1-methylethanol, etc.), linear or branched butanol (n-butanol, 1-methylpropanol, 2-methyl) Propanol etc.), linear or branched pentanol (including n-pentanol, 1-methylbutanol, 2-methylbutanol, 3-methylbutanol, etc.), linear or branched hexanol (Including n-hexanol, 1-methylpentanol, 2-methylpentanol, 3-methylpentanol, etc.), linear or branched heptanol (n-heptanol, 1-methylhexanol, 2-methylhexanol) , 3-methylhexanol, 4-methylhexanol, 5-methylhexanol, 2,4-dimethylpentanol, etc.), Chain or branched octanol (including n-octanol, 2-ethylhexanol, 1-methylheptanol, 2-methylheptanol, etc.), linear or branched nonanol (n-nonanol, 1- Methyl octanol, 3,5,5-trimethylhexanol, 1- (2′-methylpropyl) -3-methylbutanol, etc.), linear or branched decanol (n-decanol, iso-decanol, etc.) Linear) or branched undecanol (including n-undecanol, etc.), linear or branched dodecanol (including n-dodecanol, iso-dodecanol, etc.), linear or branched Tridecanol, linear or branched tetradecanol (including n-tetradecanol, iso-tetradecanol, etc.), linear or branched Pentadecanol, linear or branched hexadecanol (including n-hexadecanol, iso-hexadecanol, etc.), linear or branched heptadecanol, linear or branched And octadecanol (including n-octadecanol, iso-octadecanol, etc.), cyclopentanol, cyclohexanol, methylcyclohexanol, dimethylcyclohexanol, cycloheptanol and the like.

  Moreover, as a polyhydric alcohol, the polyhydric alcohol which has 2-8 hydroxyl groups is used preferably.

  Specific examples of the dihydric alcohol (diol) include ethylene glycol, 1,2-propanediol (propylene glycol), 1,3-propanediol, 1,4-butanediol, 1,2-butanediol, 2-methyl-1,2-propanediol, 2-methyl-1,3-propanediol, 1,3-butanediol, 1,4-butanediol, 1,2-pentanediol, 1,3-pentanediol, 1 , 4-pentanediol, 1,5-pentanediol, neopentyl glycol, 1,6-hexanediol, 2-ethyl-2-methyl-1,3-propanediol, 1,7-heptanediol, 2-methyl- 2-propyl-1,3-propanediol, 2,2-diethyl-1,3-propanediol, 1,8-octanedi Lumpur, 1,9-nonanediol, 1,10-decanediol, 1,11-decanediol, 1,12-dodecane diol. Specific examples of trihydric or higher alcohols include trimethylolethane, trimethylolpropane, trimethylolbutane, di- (trimethylolpropane), tri- (trimethylolpropane), pentaerythritol, di- ( Pentaerythritol), tri- (pentaerythritol), glycerol, polyglycerol (2 to 20 mer of glycerol), 1,3,5-pentanetriol, sorbitol, sorbitan, sorbitol glycerol condensate, adonitol, arabitol, xylitol, mannitol Polyhydric alcohol such as xylose, arabinose, ribose, rhamnose, glucose, fructose, galactose, mannose, sorbose, cellobiose, maltose, isomaltose, trehalose, shuku Over scan, raffinose, gentianose, sugars such as melezitose, and their partially etherified products and methyl glucosides (glycosides) and the like. Among these, neopentyl glycol, trimethylol ethane, trimethylol propane, trimethylol butane, di- (trimethylol propane), tri- (trimethylol propane), pentaerythritol, di- (pentaerythritol), tri- (penta Hindered alcohols such as erythritol are preferred.

  Among alcohols, a saturated monohydric alcohol having a branched chain is preferably used from the viewpoint of processability. Further, when a polyhydric alcohol is used, a so-called partial ester in which a part of the hydroxyl group is esterified may be used. Further, two or more kinds of alcohols can be mixed and used.

  The content of the alcohol is 16% by mass or more, preferably 18% by mass or more, and more preferably 20% by mass or more based on the total amount of the oil composition from the viewpoint of improving the processing efficiency and improving the tool life. From the viewpoint of handleability, it is preferably 100% by mass or less, more preferably 95% by mass or less, still more preferably 90% by mass or less, and most preferably 80% by mass or less, based on the total amount of the oil composition.

(B-2) The carboxylic acid may be a monobasic acid or a polybasic acid. From the viewpoint of improvement in processing efficiency and tool life, monovalent carboxylic acids having 1 to 40 carbon atoms are preferable, more preferably carboxylic acids having 5 to 25 carbon atoms, and most preferably 5 to 20 carbon atoms. Carboxylic acid. These carboxylic acids may be linear or branched and may be saturated or unsaturated, but are preferably saturated carboxylic acids from the standpoint of stickiness prevention. Specifically, the same thing as the monobasic acid and polybasic acid which were illustrated in description of above-mentioned ester can be mentioned.
Examples of the metal salt of the carboxylic acid include sodium, potassium, magnesium, calcium, and barium salts of the above carboxylic acid.

  (B-3) Examples of the unsaturated carboxylic acid sulfide include unsaturated sulfides of the carboxylic acid (B). Specific examples include sulfides of oleic acid.

(B-4) In the compound represented by the general formula (5), examples of the hydrocarbon group having 1 to 30 carbon atoms represented by R ⁷ include, for example, a linear or branched alkyl group having 1 to 30 carbon atoms. Group, a C5-C7 cycloalkyl group, a C6-C30 alkyl cycloalkyl group, a C2-C30 linear or branched alkenyl group, a C6-C10 aryl group, a C7-C30 And an arylalkyl group having 7 to 30 carbon atoms. In these, it is preferable that it is a C1-C30 linear or branched alkyl group, More preferably, it is a C1-C20 linear or branched alkyl group, More preferably, it is a C1-C10. A linear or branched alkyl group, most preferably a linear or branched alkyl group having 1 to 4 carbon atoms. Examples of the linear or branched alkyl group having 1 to 4 carbon atoms include a methyl group, an ethyl group, a linear or branched propyl group, and a linear or branched butyl group.

  The substitution position of the hydroxyl group is arbitrary, but when it has two or more hydroxyl groups, it is preferably substituted with an adjacent carbon atom. c is preferably an integer of 1 to 3, and more preferably 2. d is preferably an integer of 0 to 3, more preferably 1 or 2. Examples of the compound represented by the general formula (5) include p-tert-butylcatechol.

(B-5) In the compound represented by the general formula (6), examples of the hydrocarbon group having 1 to 30 carbon atoms represented by R ⁸ are represented by R ⁷ in the general formula (5). The same thing as the example of a C1-C30 hydrocarbon group made can be mentioned, and the example of a preferable thing is also the same. The substitution position of the hydroxyl group is arbitrary, but when it has two or more hydroxyl groups, it is preferably substituted with an adjacent carbon atom. e is preferably an integer of 1 to 3, more preferably 2. f is preferably an integer of 0 to 3, more preferably 1 or 2. Examples of the compound represented by the general formula (6) include 2,2-dihydroxynaphthalene and 2,3-dihydroxynaphthalene.

(B-6) As a polyoxyalkylene compound, the compound represented by the following general formula (7) or (8) can be mentioned, for example.
_{^{R 9 O- (R 10 O)}} g -R 11 (7)
[In Formula (7), R ⁹ and R ¹¹ each independently represent a hydrogen atom or a hydrocarbon group having 1 to 30 carbon atoms, R ¹⁰ represents an alkylene group having 2 to 4 carbon atoms, and g is a number average. It represents an integer having a molecular weight of 100 to 3500. ]
X-[(R ¹² O) _h -R ¹³ ] _i (8)
Wherein (8), X represents a polyvalent residue which is obtained by removing some or all of the hydrogen atoms of the hydroxyl groups of an alcohol having 3-8 hydroxyl groups, R ¹² is an alkylene group having 2 to 4 carbon atoms R ¹³ represents a hydrogen atom or a hydrocarbon group having 1 to 30 carbon atoms, h represents an integer having a number average molecular weight of 100 to 3500, and i represents the number of hydrogen atoms removed from the hydroxyl group of X Represents the same number. ]

In the general formula (7), at least one of R ⁹ and R ¹¹ is preferably a hydrogen atom. Examples of the hydrocarbon group having 1 to 30 carbon atoms represented by R ⁹ and ^{R 11,} for example, the same as the examples of the hydrocarbon group having 1 to 30 carbon atoms represented by ^{R 7} in the general formula (5) Examples of preferred ones are also the same. Specific examples of the alkylene group having 2 to 4 carbon atoms represented by R ¹⁰ include an ethylene group, a propylene group (methylethylene group), and a butylene group (ethylethylene group). e is preferably an integer such that the number average molecular weight is 300 to 2,000, and more preferably an integer such that the number average molecular weight is 500 to 1,500.

  Moreover, the polyhydric alcohol illustrated by description of (B-1) alcohol is mentioned as a specific example of the polyhydric alcohol which has 3-8 hydroxyl groups which comprise X in the said General formula (8).

Examples of the alkylene group having 2 to 4 carbon atoms represented by R ^12, there can be mentioned the same as the examples of the alkylene group having 2 to 4 carbon atoms represented by R ¹⁰ in the general formula (7) . As examples of the hydrocarbon group having 1 to 30 carbon atoms represented by R ¹³ may include the same ones as examples of the hydrocarbon group having 1 to 30 carbon atoms represented by R ⁷ in the general formula (5) Examples of preferred ones are the same. At least one of i R ¹³ is preferably a hydrogen atom, more preferably all hydrogen atoms. h is preferably an integer having a number average molecular weight of 300 to 2,000, more preferably an integer having a number average molecular weight of 500 to 1,500.

  (B-7) The constituent alcohol of the ester may be a monohydric alcohol or a polyhydric alcohol. In addition, the carboxylic acid constituting the (B-7) ester may be a monobasic acid or a polybasic acid.

  As an example of the monohydric alcohol and polyhydric alcohol which comprise ester, the same thing as the monohydric alcohol and polyhydric alcohol illustrated in description of (B-1) alcohol can be mentioned. The same applies to the more preferable ones. Moreover, as an example of the monobasic acid and polybasic acid which comprise ester, the same thing as the monobasic acid and polybasic acid which were illustrated in description of (B-2) carboxylic acid and its metal salt can be mentioned. The same applies to the more preferable ones.

  In addition, when polyhydric alcohol is used as an alcohol component, it is a complete ester in which all hydroxyl groups in the polyhydric alcohol are esterified. Further, when a polybasic acid is used as the carboxylic acid component, it may be a complete ester in which all the carboxyl groups in the polybasic acid are esterified, or a part of the carboxyl group is not esterified and remains as a carboxyl group. It may be a partial ester.

  The total number of carbon atoms of the ester as the oily agent is not particularly limited, but an ester having a total carbon number of 7 or more is preferable, and an ester of 9 or more is more preferable, from the viewpoint of improvement in processing efficiency and tool life. The above esters are most preferred. Further, from the viewpoint of not increasing the occurrence of stain and corrosion, and compatibility with organic materials, an ester having a total carbon number of 60 or less is preferable, an ester of 45 or less is more preferable, an ester of 26 or less is more preferable, and 24 The following esters are more preferred, and esters of 22 or less are most preferred.

(B-8) The polyhydric alcohol constituting the hydrocarbyl ether of the polyhydric alcohol is usually 2-8 valent, preferably 2-6 valent. Specific examples of the polyhydric alcohol having 3 to 8 hydroxyl groups are the same as those of the alcohol according to the present invention. These polyhydric alcohols may be used alone or in combination of two or more.
Preferred polyhydric alcohols include ethylene glycol, propylene glycol, neopentyl glycol, glycerin, trimethylol ethane, trimethylol propane, pentaerythritol, sorbitan, and mixtures thereof. Among these, glycerin is the most preferable from the viewpoint of improvement in processing efficiency and tool life.

  As the hydrocarbyl ether of the polyhydric alcohol, one obtained by converting a part or all of the hydroxyl groups of the polyhydric alcohol into a hydrocarbyl ether can be used. From the viewpoint of improving the processing efficiency and improving the tool life, a product obtained by converting a part of the hydroxyl group of the polyhydric alcohol into a hydrocarbyl ether (partially etherified product) is preferable. Here, the hydrocarbyl group is an alkyl group having 1 to 24 carbon atoms, an alkenyl group having 2 to 24 carbon atoms, a cycloalkyl group having 5 to 7 carbon atoms, an alkylcycloalkyl group having 6 to 11 carbon atoms, carbon A hydrocarbon group having 1 to 24 carbon atoms such as an aryl group having 6 to 10 carbon atoms, an alkylaryl group having 7 to 18 carbon atoms, and an arylalkyl group having 7 to 18 carbon atoms is represented.

  Among these hydrocarbyl groups, straight chain or branched alkyl groups having 2 to 18 carbon atoms or straight chain or branched alkenyl groups having 2 to 18 carbon atoms from the viewpoint of improving machining efficiency and tool life. Group is preferable, and a linear or branched alkyl group having 3 to 12 carbon atoms or an oleyl group (residue obtained by removing a hydroxyl group from oleyl alcohol) is more preferable.

  (B-9) Monoamine is preferably used as the amine. The carbon number of the monoamine is preferably 6 to 24, more preferably 12 to 24. The carbon number here means the total number of carbon atoms contained in the monoamine. When the monoamine has two or more hydrocarbon groups, it represents the total number of carbon atoms.

  As the monoamine used in the present embodiment, any of a primary monoamine, a secondary monoamine, and a tertiary monoamine can be used. From the viewpoint of improving machining efficiency and tool life, the primary amine is used. Monoamine is preferred.

  As the hydrocarbon group bonded to the nitrogen atom of the monoamine, any of an alkyl group, alkenyl group, cycloalkyl group, alkylcycloalkyl group, aryl group, alkylaryl group, arylalkyl group, etc. can be used. From the viewpoint of improving efficiency and tool life, an alkyl group or an alkenyl group is preferable. The alkyl group and alkenyl group may be linear or branched, but are preferably linear from the viewpoint of improvement in processing efficiency and tool life.

  Preferred monoamines used in this embodiment include, for example, hexylamine (including all isomers), heptylamine (including all isomers), octylamine (including all isomers), nonylamine ( Including all isomers), decylamine (including all isomers), undecylamine (including all isomers), dodecylamine (including all isomers), tridecylamine (including all isomers) Including), tetradecylamine (including all isomers), pentadecylamine (including all isomers), hexadecylamine (including all isomers), heptadecylamine (including all isomers) , Octadecylamine (including all isomers), nonadecylamine (including all isomers), icosylamine (including all isomers), Amine (including all isomers), docosylamine (including all isomers), tricosylamine (including all isomers), tetracosylamine (including all isomers), octadecenylamine (all (Including isomers) (including oleylamine and the like) and mixtures of two or more thereof. Among these, from the viewpoint of improvement in machining efficiency and tool life, primary monoamines having 12 to 24 carbon atoms are preferable, primary monoamines having 14 to 20 carbon atoms are more preferable, and those having 16 to 18 carbon atoms are preferable. Primary monoamines are more preferred.

  In this embodiment, only 1 type chosen from the said oil-based agent (B-1)-(B-9) may be used, and 2 or more types of mixtures may be used. Among these, (B-1) alcohol, (B-2) carboxylic acid and its metal salt, (B-3) sulfide of unsaturated carboxylic acid, and (B-7) ester because of better lubricity. It is preferable that it is 1 type, or 2 or more types of mixtures chosen from these.

  The content of the oily agent is not particularly limited, but is preferably 0.1% by mass or more, more preferably 0.5% by mass, based on the total amount of the oily agent composition, from the viewpoint of improving the processing efficiency and improving the tool life. As mentioned above, More preferably, it is 2 mass% or more. From the viewpoint of stability, the content of the oil agent is preferably 30% by mass or less, more preferably 20% by mass or less, and further preferably 15% by mass or less, based on the total amount of the oil agent.

  Moreover, it is preferable that the oil agent composition which concerns on this embodiment further contains an extreme pressure agent in order to improve workability. Preferred extreme pressure agents include sulfur compounds and phosphorus compounds described below.

The sulfur compound is not particularly limited as long as it does not impair the properties as a processing oil, but dihydrocarbyl polysulfide, sulfide ester (including sulfurized fats and oils), sulfide mineral oil, sulfurized fatty acid, zinc dithiophosphate, zinc dithiocarbamate , Molybdenum dithiophosphate and molybdenum dithiocarbamate are preferably used.
* Added deficit part.

The dihydrocarbyl polysulfide is a sulfur compound generally called polysulfide or sulfurized olefin, and specifically means a compound represented by the following general formula (5).
R ¹⁴ -S _j -R ¹⁵ (9)
[In the formula (9), R ¹⁴ and R ¹⁵ may be the same or different, and are each a linear or branched alkyl group having 3 to 20 carbon atoms, an aryl group having 6 to 20 carbon atoms, or a carbon number. It represents a 7-20 alkylaryl group or a C7-20 arylalkyl group, and j represents an integer of 2-6, preferably 2-5. ]

In the general formula (9), R ¹⁴ and R ¹⁵ are each independently a branched alkyl group having 3 to 18 carbon atoms derived from ethylene or propylene from the viewpoint of improving the processing efficiency and improving the tool life. It is more preferable that it is a branched alkyl group having 6 to 15 carbon atoms derived from ethylene or propylene.

  Specific examples of the sulfurized ester include so-called sulfurized fats and oils obtained by sulfurizing animal and vegetable fats and oils such as beef tallow, pork tallow, fish fat, rapeseed oil, and soybean oil, and unsaturated fatty acids (oleic acid, linoleic acid, or the above). (Including fatty acids extracted from animal and vegetable fats and oils) and various alcohols obtained by sulfurizing unsaturated fatty acid esters obtained by any method and mixtures of animal and vegetable oils and unsaturated fatty acid esters by any method And sulfided with

  Sulfided mineral oil refers to one obtained by dissolving elemental sulfur in mineral oil. Here, the mineral oil used in the sulfide mineral oil is not particularly limited. Specifically, the lubricating oil fraction obtained by subjecting crude oil to atmospheric distillation and vacuum distillation is subjected to solvent removal, solvent extraction, hydrocracking. , Paraffinic mineral oils, naphthenic mineral oils, etc., which are refined by appropriately combining purification treatments such as solvent dewaxing, catalytic dewaxing, hydrorefining, sulfuric acid washing, and clay treatment. In addition, as the elemental sulfur, any form such as a lump, powder, molten liquid, etc. may be used, but when powdered or molten liquid elemental sulfur is used, it is efficiently dissolved in the base oil. Is preferable. In addition, molten liquid elemental sulfur has the advantage that the melting operation can be performed in a very short time because the liquids are mixed together, but it must be handled above the melting point of elemental sulfur, heating equipment, etc. It is not always easy to handle because it requires special equipment and is handled in a high temperature atmosphere. On the other hand, powdery simple sulfur is particularly preferable because it is inexpensive and easy to handle, and the time required for dissolution is sufficiently short. Moreover, although there is no restriction | limiting in particular in sulfur content in a sulfide mineral oil, Preferably it is 0.05-1.0 mass% normally on the basis of the sulfide mineral oil whole quantity, More preferably, it is 0.1-0.5 mass%. is there.

Examples of the sulfurized fatty acid include oleic acid, linoleic acid, fatty acids extracted from animal and vegetable fats and oils, and those obtained by sulfurizing a mixture thereof.

［式（１０）〜（１３）中、Ｒ^１６、Ｒ^１７、Ｒ^１８、Ｒ^１９、Ｒ^２０、Ｒ^２１、Ｒ^２２、Ｒ^２３、Ｒ^２４、Ｒ^２５、Ｒ^２６、Ｒ^２７、Ｒ^２８、Ｒ^２９、Ｒ^３０及びＲ^３１は同一でも異なっていてもよく、それぞれ炭素数１以上の炭化水素基を表し、Ｘ^１、Ｘ^２、Ｘ^３及びＸ^４はそれぞれ酸素原子又は硫黄原子を表し、Ｘ^１とＸ^２、Ｘ^３とＸ^４はそれぞれ同一でも異なっていても良い。］ The zinc dithiophosphate compound, the zinc dithiocarbamate compound, the molybdenum dithiophosphate and the molybdenum dithiocarbamate mean compounds represented by the following general formulas (10) to (13), respectively.

[In the formulas (10) to (13), R ¹⁶ , R ¹⁷ , R ¹⁸ , R ¹⁹ , R ²⁰ , R ²¹ , R ²² , R ²³ , R ²⁴ , R ²⁵ , R ²⁶ , R ²⁷ , R ²⁸ , R ²⁹ , R ³⁰ and R ³¹ may be the same or different and each represents a hydrocarbon group having 1 or more carbon atoms; X ¹ , X ² , X ³ and X ⁴ each represents an oxygen atom or a sulfur atom; X ¹ and X ² , X ³ and X ⁴ may be the same or different. ]

  In the present embodiment, among the above sulfur compounds, when at least one selected from the group consisting of dihydrocarbyl polysulfide and sulfurized ester is used, improvement in machining efficiency and tool life can be achieved at a higher level. Therefore, it is preferable.

  Although the content of the sulfur compound is arbitrary, it is preferably 1% by mass or more, more preferably 2% by mass or more, and further preferably 3% by mass on the basis of the total amount of the oil agent from the viewpoint of improvement in machining efficiency and tool life. % Or more. Further, from the viewpoint of preventing abnormal wear, the content of the sulfur compound is preferably 50% by mass or less, more preferably 40% by mass or less, still more preferably 30% by mass or less, particularly preferably, based on the total amount of the oil composition. It is 20 mass% or less.

  In addition, as the phosphorus compound used as the extreme pressure agent in the present embodiment, specifically, phosphate ester, acidic phosphate ester, amine salt of acidic phosphate ester, chlorinated phosphate ester, phosphite ester and phosphate Examples include thiothionate. Examples of these phosphorus compounds include esters of phosphoric acid, phosphorous acid or thiophosphoric acid and alkanols, polyether type alcohols, or derivatives thereof. In the present embodiment, a compound having both a phosphorus atom and a sulfur atom in one molecule is included in the phosphorus compound for convenience.

  In the present embodiment, among the phosphorus compounds, phosphoric acid esters, acidic phosphoric acid esters, and amine salts of acidic phosphoric acid esters are preferable from the viewpoint of improving machining efficiency and improving tool life.

  Although the content of the phosphorus compound is arbitrary, it is preferably 1% by mass or more, more preferably 2% by mass or more, and further preferably 3% by mass on the basis of the total amount of the oil agent from the viewpoint of improvement of machining efficiency and improvement of tool life. % Or more. From the viewpoint of preventing abnormal wear, the content of the phosphorus compound is preferably 10% by mass or less, more preferably 5% by mass or less, still more preferably 3% by mass or less, particularly preferably, based on the total amount of the oil composition. 1% by mass or less.

  In addition, the oil composition according to the present embodiment, apart from the above oil agent, does not contain a perfluoroalkyl group for the purpose of improving processability, and is an alkylene oxide of hydroxy acid having a hydrophilic lipophilic index of 8 to 14. It is preferable to contain an adduct.

Here, the hydrophilic / lipophilic index is a mass ratio of the lipophilic group part to the hydrophilic group part of the surfactant molecule, and is calculated by the following formula.
Hydrophilic / lipophilic index = (molecular weight of hydrophilic group portion / molecular weight of entire surfactant) × 100 ÷ 5

The lipophilic group moiety referred to in the present invention is a hydrocarbon group such as an alkyl group or a cycloalkyl group. Further, the hydrophilic group part means a residue obtained by removing the lipophilic group part from the surfactant molecule. For example, in the case of the surfactant shown below, the part surrounded by the dotted line in the formula is the hydrophilic group part. .

  When the hydrophilic / lipophilic index of the alkylene oxide adduct of hydroxy acid is less than 8 or exceeds 14, the processability becomes insufficient.

  As the hydroxy acid constituting the alkylene oxide adduct of hydroxy acid, an aliphatic monohydroxy acid is preferable, and specifically, juniperic acid, ricinoleic acid, densipolylic acid, α-oxylinolenic acid, lesqueleela (Lesquerella) acid or monohydroxy acid contained in castor oil, rapeseed oil, tall oil and the like.

Specific examples of the alkylene group in the alkylene oxide include an ethylene group (—CH ₂ CH ₂ —), a propylene group (—CH (CH ₃ ) CH ₂ —), and a trimethylene group (—CH ₂ CH ₂ CH _2- ), butylene group (—CH (CH ₂ CH ₃ ) CH ₂ —), tetramethylene group (—CH ₂ CH ₂ CH ₂ CH ₂ —) and the like. Among these alkylene groups, ethylene group and propylene group are more preferable.

式中、Ｒ^３２は、炭素数７〜２３、好ましくは９〜２１、より好ましくは１１〜１９を有する炭化水素基を表し、直鎖でも分岐鎖でもよく、飽和でも不飽和でも良い。また、脂肪族ヒドロキシ酸でも芳香族ヒドロキシ酸でもよいが、不飽和で分岐鎖を有さない脂肪族モノヒドロキシ酸が好ましい。Ｒ^３３は炭素数２〜４のアルキレン基を表し、ｎはＲ^３３Ｏで表されるオキシアルキレン基の繰り返し数を表し、好ましくは１〜２０、より好ましくは２〜１５、さらに好ましくは２〜１２の整数である。また、（Ｒ^３３Ｏ）_ｎが共重合鎖である場合、ランダム共重合鎖でもブロック共重合鎖でもよいが、ランダム重合鎖であることが好ましい。 As the alkylene oxide adduct of hydroxy acid, a compound represented by the following general formula (14) is preferable.

In the formula, R ³² represents a hydrocarbon group having 7 to 23 carbon atoms, preferably 9 to 21 carbon atoms, more preferably 11 to 19 carbon atoms, which may be linear or branched and may be saturated or unsaturated. Moreover, although aliphatic hydroxy acid or aromatic hydroxy acid may be sufficient, the unsaturated monohydroxy acid which is unsaturated and does not have a branched chain is preferable. R ³³ represents an alkylene group having 2 to 4 carbon atoms, and n represents the number of repeating oxyalkylene groups represented by R ³³ O, preferably 1 to 20, more preferably 2 to 15, and still more preferably 2 to 2. It is an integer of 12. When (R ³³ O) _n is a copolymer chain, it may be a random copolymer chain or a block copolymer chain, but is preferably a random polymer chain.

  The content of the alkylene oxide adduct of hydroxy acid in the oil agent composition according to the present embodiment is not particularly limited, but is preferably 0.5 to 70% by mass, more preferably 1 to 60% by mass, based on the total amount of the oil agent composition. %, More preferably 3 to 40% by mass. If the content is less than 0.5% by mass, the blending effect is small, and if it exceeds 70% by mass, not only an effect commensurate with the blending amount can be obtained but also the workability may be lowered.

  The oil composition according to the present embodiment preferably further contains an antioxidant. Antioxidants that can be used include phenolic antioxidants, amine-based antioxidants, and those used as other food additives. Moreover, the zinc dithiophosphate compound represented by General formula (10) can also be used as antioxidant.

  As the phenol-based antioxidant, any phenol-based compound used as an antioxidant for lubricating oils can be used, and is not particularly limited. For example, an alkylphenol compound is preferable.

  As the amine-based antioxidant, any amine-based compound used as an antioxidant for lubricating oils can be used, and is not particularly limited. For example, phenyl-α-naphthylamine, Np-alkyl Preferred examples include phenyl-α-naphthylamine and p, p′-dialkyldiphenylamine, and specifically include 4-butyl-4′-octyldiphenylamine, phenyl-α-naphthylamine, octylphenyl-α-naphthylamine, dodecylphenyl. -Α-naphthylamine and mixtures thereof.

  Further, an antioxidant used as a food additive can also be used, and partially overlaps with the above-described phenolic antioxidant. For example, 2,6-di-tert-butyl-p-cresol (DBPC) ), 4,4′-methylenebis (2,6-di-tert-butylphenol), 4,4′-bis (2,6-di-tert-butylphenol), 4,4′-thiobis (6-tert-butyl) -O-cresol), ascorbic acid (vitamin C), fatty acid ester of ascorbic acid, tocopherol (vitamin E), 3,5-di-tert-butyl-4-hydroxyanisole, 2-tert-butyl-4-hydroxyanisole 3-tert-butyl-4-hydroxyanisole, 1,2-dihydro-6-ethoxy-2,2,4-trimethylquino Down (ethoxyquin), 2- (1,1-dimethyl) -1,4-benzenediol (TBHQ), can be mentioned 2,4,5-hydroxybutyronitrile phenone (THBP).

  Among these antioxidants, those used as phenolic antioxidants, amine antioxidants, and food additives are preferred. Furthermore, when importance is attached to biodegradability, what is used as the said food additive is more preferable, and among them, ascorbic acid (vitamin C), fatty acid ester of ascorbic acid, tocopherol (vitamin E), 2,6- Di-tert-butyl-p-cresol (DBPC), 3,5-di-tert-butyl-4-hydroxyanisole, 2-tert-butyl-4-hydroxyanisole, 3-tert-butyl-4-hydroxyanisole, 1,2-dihydro-6-ethoxy-2,2,4-trimethylquinoline (ethoxyquin), 2- (1,1-dimethyl) -1,4-benzenediol (TBHQ), or 2,4,5-tri Hydroxybutyrophenone (THBP) is preferred, ascorbic acid (vitamin C), fatty acid ester of ascorbic acid Ether, tocopherol (vitamin E), 2,6-di -tert- butyl -p- cresol (DBPC), or 3,5-di -tert- butyl-4-hydroxyanisole are more preferred.

  The content of the antioxidant is not particularly limited, but in order to maintain good oxidation stability, the content is preferably 0.01% by mass or more, more preferably 0.05% by mass or more based on the total amount of the oil agent. Most preferably, it is 0.1% by mass or more. On the other hand, since the improvement in the effect cannot be expected even if more are added, the content is preferably 10% by mass or less, more preferably 5% by mass or less, and most preferably 3% by mass or less.

  Moreover, the oil agent composition according to the present embodiment may contain conventionally known additives other than those described above. Examples of such additives include extreme pressure additives other than the phosphorus compounds and sulfur compounds described above (including chlorine extreme pressure agents); wetting agents such as diethylene glycol monoalkyl ether; acrylic polymers, paraffin wax, microwax, slack Film forming agents such as wax and polyolefin wax; water displacement agents such as fatty acid amine salts; solid lubricants such as graphite, graphite fluoride, molybdenum disulfide, boron nitride, polyethylene powder; amines, alkanolamines, amides, carboxylic acids, Corrosion inhibitors such as carboxylates, sulfonates, phosphoric acid, phosphates, partial esters of polyhydric alcohols; metal deactivators such as benzotriazoles and thiadiazoles; quenching of methylsilicones, fluorosilicones, polyacrylates, etc. Foaming agent; alkenyl succinimide, benzy Amine, ashless dispersants such as polyalkenyl amines polyaminoamide; and the like. The content when these known additives are used in combination is not particularly limited, but is added in such an amount that the total content of these known additives is 0.1 to 10% by mass based on the total amount of the oil composition. It is common to do.

The kinematic viscosity of the oil composition according to the present embodiment is not particularly limited, but the kinematic viscosity at 40 ° C. is preferably 200 mm ² / s or less from the viewpoint of easy supply to the processing site, and is 100 mm ² / s. It is more preferably s or less, even more preferably 75 mm ² / s or less, and particularly preferably 50 mm ² / s or less. Further, from the viewpoint of improving the processing efficiency and the tool life, the kinematic viscosity at 40 ° C. is preferably 5 mm ² / s or more, more preferably 7 mm ² / s or more, and 10 mm ² / s or more. More preferably.

  In processing with a very small amount of oil supply, several to tens of mL (preferably 1 to 90 mL / h) of oil per hour is directed to the processing part (cutting / grinding part) of the workpiece together with the compressed fluid. Supply in mist form. As the compressed fluid, in addition to compressed air, compressed fluid such as nitrogen, argon, helium and carbon dioxide can be used alone, or these fluids can be mixed and used.

  Moreover, when using the oil agent composition which concerns on this embodiment, it is preferable to supply 0.01-100 mass times water of this oil agent composition to the process site | part of a workpiece. The amount of water used is more preferably 0.01 to 100 times, more preferably 2 to 100 times, more preferably 3 to 50 times, particularly preferably 4 to 40 times, most preferably the oil agent composition. Is 5-30 mass times.

  The water supply method is not particularly limited. For example, (i) a method of supplying a mixture of an oil composition and water by misting with a compressed fluid, and (ii) supplying the oil composition and water separately by misting. And (iii) a method of supplying after mixing the oil agent composition and water separately.

  The oil composition according to the present embodiment having the above-described configuration can be suitably used for cutting, grinding, rolling, forging, and the like. Among these uses, the oil composition according to the present embodiment is very useful as an oil used for cutting, grinding, or rolling.

  Moreover, since the supply method to the process part of the oil agent composition which concerns on this embodiment can exhibit a more remarkable effect, a trace amount oil agent supply type is preferable, and it is especially preferable as a trace amount oil agent supply type oil for cutting and grinding.

  EXAMPLES Hereinafter, although this invention is demonstrated more concretely based on an Example and a comparative example, this invention is not limited to a following example at all.

（油性剤）
Ｂ１：分岐鎖状トリデカノール
Ｂ２：オレイン酸カリウム塩
Ｂ３：グリセリンモノオレート
Ｂ４：オレイルアルコール
Ｂ５：オレイン酸硫化物
（ヒロドキシ酸アルキレンオキサイド付加物）
Ｃ１：ひまし油脂肪酸とポリエチレングリコール（６モル）のモノエステル（親水新油指数９．４３
Ｃ２：リシノール酸とポリエチレングリコール（１２モル）のモノエステル（親水新油指数１２．８１）
（その他の添加剤）
Ｄ１：トリクレジルホスフェート
Ｄ２：硫化エステル
Ｄ３：２，６−ジ−ｔｅｒｔ−ブチル−ｐ−クレゾール
Ｄ４：ｐ−ｔｅｒ−ブチルカテコール [Examples 1 to 29, Comparative Examples 1 to 5]
In Examples 1 to 29 and Comparative Examples 1 to 5, oil agent compositions having the compositions shown in Tables 1 to 5 were prepared using the base oils and additives shown below, respectively. In addition, when the components of the oil composition were not completely dissolved, they were homogenized using a homogenizer and subjected to an evaluation test.
(Base oil)
Base oil a: mineral oil (kinematic viscosity at 40 ° C .: 42 mm ² / s)
Base oil b: trioleate of trimethylolpropane (kinematic viscosity at 40 ° C .: 49.3 mm ² / s)
Base oil c: poly α-olefin (kinematic viscosity at 40 ° C .: 47 mm ² / s)
(Compound having a perfluoroalkyl group)
A1: Perfluorobutylethylene oxide adduct (average addition number 5)
A2: perfluoroalkyl amine _{(C 3} F 7 _-NH 2)
A3: perfluorobutyl sulfonate sodium salt _{(C 4 F 9 -SO 3 Na} )
A4: perfluorobutyl potassium carboxylate salt _{(C 4} F 9 -COOK)
A5: perfluorobutyl sulphonamide _{(C 4 F 9 -SO 2 NH} 2)
A6: Perfluoroalkylsulfonamide represented by the following formula

(Oil-based agent)
B1: Branched tridecanol B2: Potassium oleate B3: Glycerol monooleate B4: Oleyl alcohol B5: Oleic acid sulfide (hydroxide acid alkylene oxide adduct)
C1: Castor oil fatty acid and polyethylene glycol (6 mol) monoester (hydrophilic new oil index 9.43
C2: monoester of ricinoleic acid and polyethylene glycol (12 mol) (hydrophilic new oil index 12.81)
(Other additives)
D1: tricresyl phosphate D2: sulfurized ester D3: 2,6-di-tert-butyl-p-cresol D4: p-ter-butylcatechol

[Machinability evaluation]
About the oil agent composition of Examples 1-29 and Comparative Examples 1-5, processing performance was evaluated by using diisodecyl adipate as a comparative standard oil. Specifically, first, one hole was tapped with diisodecyl adipate. Subsequently, about the material which prepared the pilot hole previously, tapping evaluation was performed by 200 hole continuous using each oil agent composition of Examples 1-27 or Comparative Examples 1-5. And about each oil agent composition, the tapping energy efficiency for every tapping 1 hole was calculated | required.
Tapping condition work material: JIS AC8A (aluminum material)
Tool diameter: 8mm
Tap pitch: 1.25mm
Tap rake angle: 1.5 degrees Tap bite angle: 10 degrees Tap pilot hole diameter: 7.4 mm
Rotation speed: 300rpm
Standard oil: DIDA (diisodecyl adipate)
Conveyance air pressure: 0.51 MPa
Continuous Workability Evaluation Method Tapping energy in the above test was measured, and tapping energy efficiency (%) was calculated using the following formula.
Tapping energy efficiency (%) = (tapping energy when diisodecyl adipate is used) / (tapping energy when using an oil composition)
The tapping energy efficiency for each hole obtained for each oil composition was examined, and if the tapping energy efficiency was less than 90%, it was determined that oil discharge failure occurred and was rejected. Then, the number of failures in the 200 holes was regarded as the number of continuous processing defects, and the discharge stability was evaluated based on this.
Furthermore, the highest tapping energy efficiency in processing 200 holes was set as the highest tapping energy efficiency. It is considered that the higher this value, the better the workability.
Water combination method A: Oil composition and water mixed in advance B: Oil composition and water are misted separately and separately supplied to the processing site C: Oil composition and water are separately misted It supplies to a process part after mixing. The obtained result is shown to Tables 1-5.

Claims (3)

At least one base oil selected from mineral oil and synthetic oil;
An oil composition for processing with an extremely small amount of oil containing a compound having a perfluoroalkyl group.   2. The oil composition for processing with an extremely small amount of oil supply according to claim 1, wherein the perfluoroalkyl group is at least one selected from a perfluoroalkylsulfonate group, a perfluoroalkylcarbonyl group, and a perfluorosulfonamide group. The trace amount oil agent supply type processing oil agent composition according to claim 1 or 2, comprising a compound having a structure represented by the following general formula (1) as the compound having a perfluoroalkyl group.

[In the formula (1), R ¹ represents an alkyl group having 1 to 12 carbon atoms or an alkenyl group having 2 to 12 carbon atoms, A represents a perfluoroalkyl group having 1 to 18 carbon atoms, B represents a hydrogen atom, A C1-C12 alkyl group, a C2-C12 alkenyl group, a C1-C12 alkanol group, a C6-C12 aryl group, or General formula (2):

(In the formula (2), ^{R 2} represents a hydrogen atom, an alkyl group having 1 to 18 carbon atoms, an alkenyl group or an aryl group having 6 to 18 carbon atoms having 2 to 18 carbon atoms, ^{R 3} is 1 to 12 carbon atoms An alkylene group or an alkenylene group having 2 to 12 carbon atoms.)
The group shown by is shown. ]