JP2007039761A - Rust-preventive oil composition - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a rust-preventive oil composition which can attain all of rust preventability, degreasing properties and storage stability at high level in a well-balance. <P>SOLUTION: The rust-preventive oil composition contains: a base oil composed of a mineral oil and/or a synthetic oil; an oxidized wax salt; and carboxylic acid. According to this rust-preventive oil composition, by jointly using the oxidized wax salt and carboxylic acid, its rust preventability owing to the oxidized wax salt can be exhibited to the maximum, and further, the degreasing properties of the rust-preventive oil composition and the solubility of the oxidized wax salt to the base oil can be sufficiently increased, thus all of the rust preventability, degreasing properties and storage stability can be attained at high level in a well balance. <P>COPYRIGHT: (C)2007,JPO&INPIT

Description

  The present invention relates to a rust preventive oil composition.

Conventionally, in the field of metal members such as steel plates, bearings, steel balls, and guide rails, rust prevention oil is used to prevent the occurrence of rust on the members. As such a rust preventive oil, for example, a rust preventive oil in which an oxidized wax salt as a rust preventive additive is added to a predetermined base oil is known. (For example, see Patent Document 1.)
JP 2002-302690 A

  However, recently, in the field of metallic members described above, higher rust prevention properties have been demanded, and even such conventional rust prevention oils may not be able to sufficiently meet such requirements. . In addition, in the conventional rust prevention oil, when the amount of the oxidized wax salt is increased in order to improve the rust prevention property, the degreasing property and the storage stability become insufficient.

  The present invention has been made in view of such circumstances, and provides a rust-preventing oil composition capable of achieving all of rust prevention, degreasing and storage stability at a high level in a well-balanced manner. With the goal.

  In order to solve the above problems, the rust preventive oil composition of the present invention is characterized by containing a base oil composed of mineral oil and / or synthetic oil, an oxidized wax salt, and a carboxylic acid.

  In the rust preventive oil composition of the present invention, the combined use of an oxidized wax salt and a carboxylic acid can maximize the rust preventive properties derived from the oxidized wax salt, and the rust preventive oil composition The degreasing property and the solubility of the oxidized wax salt in the base oil can be sufficiently enhanced. Therefore, according to the rust prevention oil composition of the present invention, it is possible to achieve all of rust prevention, degreasing and storage stability at a high level in a well-balanced manner.

  ADVANTAGE OF THE INVENTION According to this invention, it becomes possible to provide the rust prevention oil composition which can achieve all of rust prevention property, degreasing property, and storage stability with a high level with sufficient balance.

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

  The rust preventive oil composition of the present invention includes a base oil composed of mineral oil and / or synthetic oil.

  Specifically, as mineral oils, solvent degreasing, solvent extraction, hydrocracking, solvent dewaxing, catalytic dewaxing, hydrogen removal from lubricating oil fractions obtained by atmospheric and vacuum distillation of crude oil Examples thereof include paraffinic or naphthenic mineral oil obtained by appropriately combining one or more purification means of chemical purification, sulfuric acid washing, and clay treatment.

  Moreover, polyolefin, alkylbenzene, etc. are used suitably as synthetic oil.

  Examples of the polyolefin include those obtained by homopolymerization or copolymerization of olefin monomers having 2 to 16 carbon atoms, preferably 2 to 12 carbon atoms, and hydrides of these polymers. In the case where the polyolefin is a copolymer of olefin monomers having different structures, the monomer ratio and the monomer arrangement in the copolymer are not particularly limited, and among random copolymers, alternating copolymers and block copolymers. Any of these may be used. The olefin monomer may be any of α-olefin, internal olefin, linear olefin, and branched olefin. Specific examples of such olefin monomers include ethylene, propylene, 1-butene, 2-butene, isobutene, linear or branched pentene (including α-olefin and internal olefin), linear Or branched hexene (including α-olefin and internal olefin), linear or branched heptene (including α-olefin and internal olefin), linear or branched octene (α-olefin) ), Linear or branched nonene (α-olefin, including internal olefin), linear or branched decene (including α-olefin, internal olefin), linear Alternatively, branched undecene (including α-olefin and internal olefin), linear or branched dodecene (including α-olefin and internal olefin), linear Or branched tridecene (including α-olefin and internal olefin), linear or branched tetradecene (including α-olefin and internal olefin), linear or branched pentadecene (α-olefin) ), Linear or branched hexadecene (α-olefin, including internal olefin), and mixtures thereof. Among these, ethylene, propylene, 1-butene, 2- Butene, isobutene, an α-olefin having 5 to 12 carbon atoms and a mixture thereof are preferably used. Further, among the α-olefins having 5 to 12 carbon atoms, 1-octene, 1-decene, 1-dodecene, a mixture thereof, and the like are more preferable.

  The above-mentioned polyolefin can be produced conventionally. Specifically, for example, it can be produced by a non-catalytic thermal reaction, and an organic peroxide catalyst such as benzoyl peroxide; aluminum chloride, aluminum chloride-polyhydric alcohol, aluminum chloride-titanium tetrachloride, chloride Friedel-Crafts type catalysts such as aluminum-alkyltin halides and boron fluoride; Ziegler type catalysts such as organic aluminum chloride-titanium tetrachloride and organic aluminum-titanium tetrachloride; aluminoxane-zirconocene, ionic compound-zirconocene A metallocene catalyst such as a catalyst; a Lewis acid complex catalyst such as an aluminum chloride-base catalyst, a boron fluoride-base catalyst, etc. Polyolefins can be produced.

  Polyolefins obtained by such a method usually have double bonds, but in the present invention, so-called polyolefin hydrides obtained by hydrogenating double bond carbons in these polyolefins are used as base oils. It is preferable. When a hydride of polyolefin is used, the thermal / oxidative stability of the obtained rust preventive oil composition tends to be improved. The hydride of polyolefin can be obtained, for example, by hydrogenating polyolefin with hydrogen in the presence of a known hydrogenation catalyst and saturating double bonds existing in the polyolefin. In addition, when the olefin polymerization reaction is performed, by selecting the catalyst to be used, the olefin polymerization and the double bond existing in the polymer can be performed without passing through two steps such as olefin polymerization and polymer hydrogenation. It is also possible to complete the hydrogenation in one step.

  Among the polyolefins preferably used as a base oil in the present invention, an ethylene-propylene copolymer, polybutene (butane-butene fraction (by-product of 1-butene, 2-butene and A copolymer obtained by polymerization of a mixture of isobutene), 1-octene oligomer, 1-decene oligomer, 1-dodecene oligomer and their hydrides, and also a mixture thereof are heat / oxidative stability, viscosity- Preferred in terms of excellent temperature characteristics and low temperature fluidity, especially ethylene-propylene copolymer hydride, polybutene hydride, 1-octene oligomer hydride, 1-decene oligomer hydride, 1-dodecene oligomer hydride and These mixtures are more preferred. Synthetic oils such as ethylene-propylene copolymers, polybutenes, and poly-α-olefins that are commercially available as base oils for lubricants are usually those whose double bonds are already hydrogenated. In the invention, these commercially available products can also be used as the base oil.

  Moreover, as an alkylbenzene used suitably as a base oil concerning this invention, what has 1-4 C1-C40 alkyl groups in a molecule | numerator is preferable. Specific examples of the alkyl group having 1 to 40 carbon atoms include a methyl group, an ethyl group, a propyl group (including all isomers), a butyl group (including all isomers), and a pentyl group ( All isomers included, hexyl group (including all isomers), heptyl group (including all isomers), octyl group (including all isomers), nonyl group (including all isomers) ), Decyl group (including all isomers), undecyl group (including all isomers), dodecyl group (including all isomers), tridecyl group (including all isomers), tetradecyl group (all ), Pentadecyl group (including all isomers), hexadecyl group (including all isomers), heptadecyl group (including all isomers), octadecyl group (including all isomers) ), Nonadecyl group (including all isomers), icosyl group (including all isomers), heicosyl group (including all isomers), docosyl group (including all isomers), tricosyl group (all ), Tetracosyl group (including all isomers), pentacosyl group (including all isomers), hexacosyl group (including all isomers), heptacosyl group (including all isomers) , Octacosyl group (including all isomers), nonacosyl group (including all isomers), triacontyl group (including all isomers), hentriacontyl group (including all isomers), dotriacontyl group ( All isomers), tritriacontyl group (including all isomers), tetratriacontyl group (including all isomers), pentato Acontyl group (including all isomers), hexatriacontyl group (including all isomers), heptatriacontyl group (including all isomers), octatriacontyl group (including all isomers) ), Nonatoriacontyl group (including all isomers), tetracontyl group (including all isomers), and the like. Further, the alkyl group of the alkylbenzene according to the present invention may be linear or branched, but a branched alkyl group is preferable from the viewpoint of stability, viscosity characteristics, etc., and particularly easily available. In view of the above, branched alkyl groups derived from olefin oligomers such as propylene, butene and isobutylene are more preferred.

  The number of alkyl groups in the alkylbenzene used in the present invention is preferably 1 to 4, but from the viewpoints of stability and availability, alkylbenzene having one or two alkyl groups, that is, monoalkylbenzene, dialkylbenzene, Or a mixture thereof is most preferred. Moreover, as alkylbenzene, not only the alkylbenzene of a single structure but the mixture of the alkylbenzene which has a different structure may be sufficient.

  The alkylbenzene according to the present invention can be produced, for example, using an aromatic compound as a raw material and using an alkylating agent and an alkylation catalyst. Here, specific examples of the aromatic compound used as a raw material include benzene, toluene, xylene, ethylbenzene, methylethylbenzene, diethylbenzene, and mixtures thereof. Further, as the alkylating agent, specifically, a lower monoolefin such as ethylene, propylene, butene, and isobutylene, preferably a linear or branched olefin having 6 to 40 carbon atoms obtained by polymerization of propylene; C6-C40 linear or branched olefins obtained by thermal decomposition of wax, heavy oil, petroleum fractions, polyethylene, polypropylene, etc .; n-paraffins are separated from petroleum fractions such as kerosene and light oil And a straight-chain olefin having 9 to 40 carbon atoms obtained by olefinating it with a catalyst, and a mixture thereof. Furthermore, as alkylation catalysts in the alkylation, Friedel-Crafts type catalysts such as aluminum chloride and zinc chloride; acidic catalysts such as sulfuric acid, phosphoric acid, silicotungstic acid, hydrofluoric acid, activated clay, etc. A well-known catalyst is mentioned.

In the present invention, the kinematic viscosities of the various base oils at 40 ° C. are usually selected from the range of 1 to 1000 mm ² / s, preferably ² to 100 mm ² / s, more preferably 3 to 95 mm ² / s. A base oil may be used individually by 1 type, and 2 or more types of base oils may be mixed and used for it. In the rust preventive oil composition of the present invention, a heavy base oil having a kinematic viscosity at 40 ° C. of 100 mm ² / s or more, for example, 100 to 1000 mm ² / s, preferably 200 to 500 mm ² / s. The content of the heavy group is not particularly limited, but from the viewpoint of optimizing the thickening of the coating film of the rust preventive oil composition in the present invention, the suppression of the increase in the amount taken out, and the degreasing and spraying properties. The oil content is preferably 1 to 40% by mass, more preferably 5 to 15% by mass, based on the total amount of the composition. When the rust preventive oil composition of the present invention is composed of a base oil, an oxidized wax salt and a carboxylic acid, the content of the base oil in the rust preventive oil composition excludes the oxidized wax salt and carboxylic acid. It can be the rest. Further, as will be described later, the rust preventive oil composition of the present invention can contain additives other than oxidized wax and carboxylic acid, and the content of the base oil in this case includes oxidized wax salt, carboxylic acid and other components. The remainder except the additive may be used.

  Moreover, the rust preventive oil composition of the present invention contains an oxidized wax salt. As the oxidized wax salt, an oxidized wax obtained by oxidizing a wax and at least one selected from an alkali metal, an alkaline earth metal (excluding barium) and an amine are reacted to produce an oxidized wax. A salt obtained by neutralizing some or all of the acidic groups is preferred.

  Although it does not restrict | limit especially as an oxidation wax used as a raw material of an oxidation wax salt, For example, the paraffin wax obtained at the time of refinement | purification of a petroleum fraction, microcrystalline wax, petrolatum, polyolefin wax obtained by synthesis, etc. And the like produced by oxidizing the wax.

  When the oxidized wax salt is an alkali metal salt, examples of the alkali metal used as a raw material include sodium and potassium.

  When the oxidized wax salt is an alkaline earth metal salt, examples of the alkaline earth metal used as a raw material include magnesium, calcium, barium and the like.

  When the oxidized wax salt is a heavy metal salt, examples of the heavy metal used as a raw material include zinc and lead.

  In addition, from the viewpoint of safety with respect to the human body and biological system, it is preferable that the oxidized wax salt is not a barium salt or a heavy metal salt.

  When the oxidized wax salt is an amine salt, examples of the amine include monoamines, polyamines, and alkanolamines.

Specific examples of monoamines include monomethylamine, dimethylamine, trimethylamine, monoethylamine, diethylamine, triethylamine, monopropylamine (including all isomers), dipropylamine (including all isomers), and tripropyl. Amine (including all isomers), monobutylamine (including all isomers), dibutylamine (including all isomers), tributylamine (including all isomers), monopentylamine (all isomers) ), Dipentylamine (including all isomers), tripentylamine (including all isomers), monohexylamine (including all isomers), dihexylamine (including all isomers) , Monoheptylamine (including all isomers), diheptylamine (including all isomers), Nooctylamine (including all isomers), dioctylamine (including all isomers), monononylamine (including all isomers), monodecylamine (including all isomers), monoundecyl (all ), Monododecylamine (including all isomers), monotridecylamine (including all isomers), monotetradecylamine (including all isomers), monopentadecylamine (including all isomers) Including all isomers), monohexadecylamine (including all isomers), monoheptadecylamine (including all isomers), monooctadecylamine (including all isomers), monononadecylamine (Including all isomers), monoicosylamine (including all isomers), monohenicosylamine (including all isomers), monodocosylamine Including all isomers), monotricosylamine (including all isomers), dimethyl (ethyl) amine, dimethyl (propyl) amine (including all isomers), dimethyl (butyl) amine (all isomers) ), Dimethyl (pentyl) amine (including all isomers), dimethyl (hexyl) amine (including all isomers), dimethyl (heptyl) amine (including all isomers), dimethyl (octyl) Amine (including all isomers), dimethyl (nonyl) amine (including all isomers), dimethyl (decyl) amine (including all isomers), dimethyl (undecyl) amine (including all isomers) ), Dimethyl (dodecyl) amine (including all isomers), dimethyl (tridecyl) amine (including all isomers), dimethyl (tetradecyl) amine Min (including all isomers), dimethyl (pentadecyl) amine (including all isomers), dimethyl (hexadecyl) amine (including all isomers), dimethyl (heptadecyl) amine (including all isomers) ), Dimethyl (octadecyl) amine (including all isomers), dimethyl (nonadecyl) amine (including all isomers), dimethyl (icosyl) amine (including all isomers), dimethyl (henicosyl) amine ( Alkylamines such as all isomers), dimethyl (tricosyl) amine (including all isomers);
Monovinylamine, divinylamine, trivinylamine, monopropenylamine (including all isomers), dipropenylamine (including all isomers), tripropenylamine (including all isomers), monobutenylamine (Including all isomers), dibutenylamine (including all isomers), tributenylamine (including all isomers), monopentenylamine (including all isomers), dipentenylamine (all isomers) ), Tripentenylamine (including all isomers), monohexenylamine (including all isomers), dihexenylamine (including all isomers), monoheptenylamine (all isomers) ), Diheptenylamine (including all isomers), monooctenylamine (including all isomers), dioctenylamine (Including all isomers), monononenylamine (including all isomers), monodecenylamine (including all isomers), monoundecenyl (including all isomers), monododecenylamine (Including all isomers), monotridecenylamine (including all isomers), monotetradecenylamine (including all isomers), monopentadecenylamine (including all isomers), Monohexadecenylamine (including all isomers), monoheptadecenylamine (including all isomers), monooctadecenylamine (including all isomers), monononadecenylamine (all isomers) ), Monoicosenylamine (including all isomers), monohenicocenylamine (including all isomers), monodocosenylamine (including all isomers), Trichoderma cell (including all isomers) cycloalkenyl amines alkenyl amines, such as;
Dimethyl (vinyl) amine, dimethyl (propenyl) amine (including all isomers), dimethyl (butenyl) amine (including all isomers), dimethyl (pentenyl) amine (including all isomers), dimethyl ( Hexenyl) amine (including all isomers), dimethyl (heptenyl) amine (including all isomers), dimethyl (octenyl) amine (including all isomers), dimethyl (nonenyl) amine (all isomers) ), Dimethyl (decenyl) amine (including all isomers), dimethyl (undecenyl) amine (including all isomers), dimethyl (dodecenyl) amine (including all isomers), dimethyl (tridecenyl) Amine (including all isomers), dimethyl (tetradecenyl) amine (including all isomers), dimethyl (pen Decenyl) amine (including all isomers), dimethyl (hexadecenyl) amine (including all isomers), dimethyl (heptadecenyl) amine (including all isomers), dimethyl (octadecenyl) amine (all isomers) ), Dimethyl (nonadecenyl) amine (including all isomers), dimethyl (icosenyl) amine (including all isomers), dimethyl (henicosenyl) amine (including all isomers), dimethyl (tricosenyl) Monoamines having alkyl and alkenyl groups such as amines (including all isomers);
Monobenzylamine, (1-phenyltyl) amine, (2-phenylethyl) amine (also known as monophenethylamine), dibenzylamine, bis (1-phenethyl) amine, bis (2-phenylethylene) amine (also known as diphenethylamine) Aromatic substituted alkylamines such as
C5-C16 cycloalkylamines such as monocyclopentylamine, dicyclopentylamine, tricyclopentylamine, monocyclohexylamine, dicyclohexylamine, monocycloheptylamine, dicycloheptylamine;
Monoamines having an alkyl group and a cycloalkyl group, such as dimethyl (cyclopentyl) amine, dimethyl (cyclohexyl) amine, dimethyl (cycloheptyl) amine;
(Methylcyclopentyl) amine (including all substituted isomers), bis (methylcyclopentyl) amine (including all substituted isomers), (dimethylcyclopentyl) amine (including all substituted isomers), bis (dimethylcyclopentyl) ) Amine (including all substituted isomers), (ethylcyclopentyl) amine (including all substituted isomers), bis (ethylcyclopentyl) amine (including all substituted isomers), (methylethylcyclopentyl) amine ( All substituted isomers included), bis (methylethylcyclopentyl) amine (including all substituted isomers), (diethylcyclopentyl) amine (including all substituted isomers), (methylcyclohexyl) amine (all substituted isomers) Isomers), bis (methylcyclohexyl) amine (all substituted isomers) ), (Dimethylcyclohexyl) amine (including all substituted isomers), bis (dimethylcyclohexyl) amine (including all substituted isomers), (ethylcyclohexyl) amine (including all substituted isomers), bis (Ethylcyclohexyl) amine (including all substituted isomers), (Methylethylcyclohexyl) amine (including all substituted isomers), (Diethylcyclohexyl) amine (including all substituted isomers), (Methylcycloheptyl) ) Amine (including all substituted isomers), bis (methylcycloheptyl) amine (including all substituted isomers), (dimethylcycloheptyl) amine (including all substituted isomers), (ethylcycloheptylamine) (Including all substituted isomers), (methylethylcycloheptyl) amine (all substituted isomers) And alkyl cycloalkylamines such as (diethylcycloheptyl) amine (including all substituted isomers), etc. In addition, monoamines herein include monoamines derived from fats and oils (such as beef tallow amines) ) Is also included.

Specific examples of polyamines include ethylenediamine, diethylenetriamine, triethylenetetramine, tetraethylenepentamine, pentaethylenehexamine, propylenediamine, dipropylenetriamine, tripropylenetetramine, tetrapropylenepentamine, pentapropylenehexamine, butylenediamine. , Alkylene polyamines such as dibutylene triamine, butylene tetramine, tetrabutylene pentamine, pentabylene hexamine;
N-methylethylenediamine, N-ethylethylenediamine, N-propylethylenediamine (including all isomers), N-butylethylenediamine (including all isomers), N-pentylethylenediamine (including all isomers), N -Hexylethylenediamine (including all isomers), N-heptylethylenediamine (including all isomers), N-octylethylenediamine (including all isomers), N-nonylethylenediamine (including all isomers) N-decylethylenediamine (including all isomers), N-undecyl (including all isomers), N-dodecylethylenediamine (including all isomers), N-tridecylethylenediamine (including all isomers) Including), N-tetradecylethylenediamine (including all isomers), -Pentadecylethylenediamine (including all isomers), N-hexadecylethylenediamine (including all isomers), N-heptadecylethylenediamine (including all isomers), N-octadecylethylenediamine (all isomers) N-nonadecylethylenediamine (including all isomers), N-icosylethylenediamine (including all isomers), N-henicosylethylenediamine (including all isomers), N-doco N-alkylethylenediamines such as silethylenediamine (including all isomers), N-tricosylethylenediamine (including all isomers);
N-vinylethylenediamine, N-propenylethylenediamine (including all isomers), N-butenylethylenediamine (including all isomers), N-pentenylethylenediamine (including all isomers), N-hexenylethylenediamine ( Including all isomers), N-heptenylethylenediamine (including all isomers), N-octenylethylenediamine (including all isomers), N-nonenylethylenediamine (including all isomers), N-decenylethylenediamine (including all isomers), N-undecenyl (including all isomers), N-dodecenylethylenediamine (including all isomers), N-tridecenylethylenediamine (including all isomers) All isomers), N-tetradecenylethylenediamine (including all isomers), N- Ntadecenylethylenediamine (including all isomers), N-hexadecenylethylenediamine (including all isomers), N-heptadecenylethylenediamine (including all isomers), N-octade Cenylethylenediamine (including all isomers), N-nonadecenylethylenediamine (including all isomers), N-icosenylethylenediamine (including all isomers), N-henicocenylethylenediamine N-alkenylethylenediamine such as (including all isomers), N-docosenylethylenediamine (including all isomers), N-tricosenylethylenediamine (including all isomers);
N-alkyldiethylenetriamine, N-alkenyldiethylenetriamine, N-alkyltriethylenetetramine, N-alkenyltriethylenetetramine, N-alkyltetraethylenepentamine, N-alkenyltetraethylenepentamine, N-alkylpentaethylenehexamine, N-alkenyl Pentaethylenehexamine, N-alkylpropylenediamine, N-alkenylpropylenediamine, N-alkyldipropylenetriamine, N-alkenyldipropylenetriamine, N-alkyltripropylenetetramine, N-alkenyltripropylenetetramine, N-alkyltetrapropylenepenta Min, N-alkenyltetrapropylenepentamine, N-alkylpentapropylenehexamine, N-alkenylpentapropylene Hexamine, N-alkylbutylenediamine, N-alkenylbutylenediamine, N-alkyldibutylenetriamine, N-alkenyldibutylenetriamine, N-alkyltributylenetetramine, N-alkenyltributylenetetramine, N-alkyltetrabutylenepentamine, N-alkyl or N-alkenyl alkylene polyamines such as N-alkenyltetrabutylenepentamine, N-alkylpentabylenehexamine, N-alkenylpentabylenehexamine and the like. The polyamine referred to here also includes polyamines derived from fats and oils (such as beef tallow polyamine).

  Further, as the alkanolamine, specifically, monomethanolamine, dimethanolamine, trimethanolamine, monoethanolamine, diethanolamine, triethanolamine, mono (n-propanol) amine, di (n-propanol) amine, Tri (n-propanol) amine, monoisopropanolamine, diisopropanolamine, triisopropanolamine, monobutanolamine (including all isomers), dibutanolamine (including all isomers), tributanolamine (all Isomers), monopentanolamine (including all isomers), dipentanolamine (including all isomers), tripentanolamine (including all isomers), monohexanolamine (all Isomers), di Xanolamine (including all isomers), monoheptanolamine (including all isomers), diheptanolamine (including all isomers), monooctanolamine (including all isomers), Monononanolamine (including all isomers), monodecanolamine (including all isomers), monoundecanolamine (including all isomers), monododecanolamine (including all isomers) ), Monotridecanolamine (including all isomers), monotetradecanolamine (including all isomers), monopentadecanolamine (including all isomers), monohexadecanolamine (including all isomers) All isomers), diethyl monoethanolamine, diethyl monopropanolamine (including all isomers), diethyl monobutanol amine (Including all isomers), diethylmonopentanolamine (including all isomers), dipropylmonoethanolamine (including all isomers), dipropylmonopropanolamine (including all isomers) ), Dipropylmonobutanolamine (including all isomers), dipropylmonopentanolamine (including all isomers), dibutylmonoethanolamine (including all isomers), dibutylmonopropanolamine (all ), Dibutylmonobutanolamine (including all isomers), dibutylmonopentanolamine (including all isomers), monoethyldiethanolamine, monoethyldipropanolamine (including all isomers) ), Monoethyldibutanolamine (including all isomers), monoethyldipenta Nolamine (including all isomers), monopropyldiethanolamine (including all isomers), monopropyldipropanolamine (including all isomers), monopropyldibutanolamine (including all isomers), Monopropyldipentanolamine (including all isomers), monobutyldiethanolamine (including all isomers), monobutyldipropanolamine (including all isomers), monobutyldibutanolamine (all isomers) ), Monobutyldipentanolamine (including all isomers), monocyclohexyl monoethanolamine, monocyclohexyldiethanolamine, monocyclohexylmonopropanolamine (including all isomers), monocyclohexyldipropanolamine ( Includes all isomers ), And the like.

  Among the above-mentioned amines, monoamines are preferable in that they have good stain resistance. Among monoamines, monoamines having alkylamines, alkyl groups and alkenyl groups, monoamines having alkyl groups and cycloalkyl groups, cycloalkylamines and alkyls. Cycloalkylamine is more preferred. An amine having a total carbon number of 3 or more in the amine molecule is preferable in terms of good stain resistance, and an amine having a total carbon number of 5 or more is more preferable.

  In the present invention, as the oxidized wax salt, one of the above alkali metal salts, alkaline earth metal salts, heavy metal salts or amine salts can be used alone or in combination of two or more. From the viewpoint of properties, it is preferably at least one selected from alkali metal salts and alkaline earth metal salts, and more preferably alkaline earth metal salts. Furthermore, among alkaline earth metal salts, calcium salts are particularly preferable from the viewpoints of safety and higher combined effect with carboxylic acid.

  The content of the oxidized wax salt in the rust prevention oil composition of the present invention is not particularly limited, but from the viewpoint of rust prevention properties, it is preferably 0.5% by mass or more, more preferably 1% by mass based on the total amount of the composition. As mentioned above, More preferably, it is 2 mass% or more. The content of the oxidized wax salt is preferably 5% by mass or less, more preferably 4% by mass or less, and further preferably 3% by mass or less, based on the total amount of the composition, from the viewpoint of degreasing and storage stability. is there.

  In addition, as the carboxylic acid contained in the rust preventive oil composition of the present invention, any can be used, but preferably, fatty acid, dicarboxylic acid, hydroxy fatty acid, naphthenic acid, resin acid, oxidized wax, lanolin fatty acid and the like are used. Can be mentioned.

  Although the carbon number of the fatty acid used in the present invention is not particularly limited, it is preferably 6 to 24, more preferably 10 to 22. The fatty acid used in the present invention may be a saturated fatty acid or an unsaturated fatty acid, and may be a linear fatty acid or a branched fatty acid. Specific examples of such fatty acids include hexanoic acid (including all isomers), heptanoic acid (including all isomers), octanoic acid (including all isomers), nonanoic acid (all Isomers), decanoic acid (including all isomers), undecanoic acid (including all isomers), dodecanoic acid (including all isomers), tridecanoic acid (including all isomers), Tetradecanoic acid (including all isomers), pentadecanoic acid (including all isomers), hexadecanoic acid (including all isomers), heptadecanoic acid (including all isomers), octadecanoic acid (all isomers) ), Nonadecanoic acid (including all isomers), icosanoic acid (including all isomers), heicosanoic acid (including all isomers), docosanoic acid (including all isomers), tricosane Acid (all isomeric Saturated fatty acids such as tetracosanoic acid (including all isomers); hexenoic acid (including all isomers), heptenoic acid (including all isomers), octenoic acid (including all isomers) ), Nonenoic acid (including all isomers), decenoic acid (including all isomers), undecenoic acid (including all isomers), dodecenoic acid (including all isomers), tridecenoic acid (all ), Tetradecenoic acid (including all isomers), pentadecenoic acid (including all isomers), hexadecenoic acid (including all isomers), heptadecenoic acid (including all isomers) , Octadecenoic acid (including all isomers), nonadecenoic acid (including all isomers), icosenoic acid (including all isomers), henicosenoic acid (including all isomers), docosenoic acid (all Including isomers) And mixtures thereof; (including all isomers) tricosenoic acid, (including all isomers) tetracosenoic acid unsaturated fatty acids such as.

  As the dicarboxylic acid, preferably a dicarboxylic acid having 2 to 40 carbon atoms, more preferably a dicarboxylic acid having 5 to 36 carbon atoms is used. Among these, dimer acid, alkyl or alkenyl succinic acid obtained by dimerizing an unsaturated fatty acid having 6 to 18 carbon atoms is preferably used. Specific examples of the dimer acid include dimer acid of oleic acid. Among alkyl or alkenyl succinic acids, alkenyl succinic acid is preferable, and alkenyl succinic acid having an alkenyl group having 8 to 18 carbon atoms is more preferable.

  As the hydroxy fatty acid, a hydroxy fatty acid having 6 to 24 carbon atoms is preferably used. The hydroxy fatty acid may have one or more hydroxy groups, but those having 1 to 3 hydroxy groups are preferably used. Specific examples of such hydroxy fatty acids include ricinoleic acid and the like.

  Naphthenic acid is a carboxylic acid in petroleum having a —COOH group bonded to a naphthene ring.

  The resin acid refers to an organic acid present in a free state or as an ester in the natural resin.

  The oxidized wax is obtained by oxidizing a wax. The wax used as the raw material is not particularly limited, and specific examples include paraffin wax obtained during refining of petroleum fractions, microcrystalline wax, petratum, and polyolefin wax obtained by synthesis.

  Lanolin fatty acid is a carboxylic acid obtained by purifying (hydrolyzing, etc.) a waxy substance adhering to sheep wool.

  Among these carboxylic acids, dicarboxylic acid is preferable, dimer acid is more preferable, and dimer acid of oleic acid is more preferable from the viewpoint of rust prevention property, degreasing property, and storage stability.

  The content of carboxylic acid in the rust preventive oil composition of the present invention is not particularly limited, but is preferably 0.01% by mass or more, more preferably 0.03% by mass or more, and still more preferably 0, based on the total amount of the composition. 0.05% by mass or more. When the content of carboxylic acid is less than the lower limit, the effect of improving rust prevention due to the addition tends to be insufficient. The carboxylic acid content is preferably 0.5% by mass or less, more preferably 0.3% by mass or less, and still more preferably 0.2% by mass or less, based on the total amount of the composition. If the content of carboxylic acid exceeds the upper limit, the solubility in the base oil becomes insufficient, and the storage stability tends to decrease.

  Further, the content ratio of the oxidized wax salt and the carboxylic acid is not particularly limited, but the ratio (mass ratio) of the carboxylic acid / oxidized wax salt is preferably 1/100 to 30/100, and 3/100 to 7 / 100 is more preferable, and 4/100 to 6/100 is still more preferable. When the ratio of carboxylic acid / oxidized wax salt is less than 1/100 or more than 30/100, the effect of improving the rust prevention property, degreasing property and storage stability by the combination of both tends to be insufficient. .

  The rust preventive oil composition of the present invention may be composed of the above base oil, oxidized wax salt and carboxylic acid, but may further contain various additives as described below as required.

  The rust preventive oil composition of the present invention may further contain a rust preventive additive such as sulfonate, carboxylate, ester, sarcosine, amine, boron compound and the like.

  Preferred examples of the sulfonate include alkali metal sulfonate, alkaline earth metal sulfonate, and amine sulfonate. All sulfonates have sufficiently high safety for the human body and ecosystem, and can be obtained by reacting an alkali metal, alkaline earth metal or amine with sulfonic acid.

  Examples of the alkali metal and alkaline earth metal constituting the sulfonate include the alkali metal and alkaline earth metal exemplified in the description of the alkali metal salt and alkaline earth metal salt of the oxidized wax, respectively. Calcium is preferred.

  Examples of the amine constituting the sulfonate include the amines exemplified in the description of the amine salt of the oxidized wax. Among these, monoamines are preferable in terms of more excellent anti-rust properties. Among monoamines, alkylamines, monoamines having an alkyl group and alkenyl group, monoamines having an alkyl group and cycloalkyl group, cycloalkylamines and alkylcycloalkylamines are more preferable. preferable. An amine having a total carbon number of 3 or more in the amine molecule is preferred because it is more excellent in rust prevention, and an amine having a total carbon number of 5 or more is more preferred.

  On the other hand, as the sulfonic acid according to the present invention, a conventionally known sulfonic acid produced by a conventional method can be used. 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. Synthesis of sulfonated alkylbenzene having linear or branched alkyl groups or sulfonated alkylnaphthalene such as dinonylnaphthalene obtained as a by-product or alkylating polyolefin with benzene And sulfonic acid. Although there is no restriction | limiting in particular about the molecular weight of these sulfonic acids, Preferably it is 100-1500, More preferably, the thing of 200-700 is used.

Among the above sulfonic acids,
Dialkylnaphthalenesulfonic acid wherein the total number of carbon atoms of the two alkyl groups bonded to the naphthalene ring is 14-30;
Two alkyl groups bonded to the benzene ring are each a branched alkyl group having one linear alkyl group or one side chain methyl group, and a dialkylbenzene sulfone having a total carbon number of 14 to 30 of the two alkyl groups An acid; and a monoalkylbenzenesulfonic acid in which the alkyl bonded to the benzene ring has 15 or more carbon atoms,
It is preferable to use at least one selected from the group consisting of

  As described above, the dialkylnaphthalenesulfonic acid preferably used in the present invention has a total number of carbon atoms of two alkyl groups bonded to the naphthalene ring of 14 to 30. When the total number of carbon atoms of the two alkyl groups is less than 14, the demulsibility tends to be insufficient, and when it exceeds 30, the storage stability of the obtained rust preventive oil composition tends to be lowered. Note that each of the two alkyl groups may be linear or branched. Moreover, if the total carbon number of two alkyl groups is 14-30, there will be no restriction | limiting in particular about the carbon number of each alkyl group, However, It is preferable that the carbon number of each alkyl group is 6-18, respectively.

  Further, as described above, the dialkylbenzenesulfonic acid preferably used in the present invention is a branched alkyl group in which two alkyl groups bonded to the benzene ring each have one linear alkyl group or one side chain methyl group. And the total number of carbon atoms of the two alkyl groups is 14-30. In the case of monoalkylbenzenesulfonic acid, it can be suitably used as long as the alkyl group has 15 or more carbon atoms, as will be described later. However, when a monoalkylbenzenesulfonic acid having an alkyl group having less than 15 carbon atoms is used, rust prevention oil is used. The storage stability of the composition tends to decrease. Also, when an alkylbenzene sulfonic acid having 3 or more alkyl groups is used, the storage stability of the rust preventive oil composition tends to decrease. Further, the alkyl group bonded to the benzene ring of the dialkylbenzenesulfonic acid has a branched alkyl group having a branched structure other than the side chain methyl group (for example, a branched alkyl group having a side chain ethyl group, etc.) or two A branched alkyl group having the above branched structure (for example, a branched alkyl group derived from an oligomer of propylene) may adversely affect the human body or ecosystem, and has rust prevention properties. It tends to be insufficient. Furthermore, if the total number of carbon atoms of the two alkyl groups bonded to the benzene ring of the dialkylbenzene sulfonic acid is less than 14, the demulsibility tends to be reduced. The stability tends to decrease. In addition, as long as the total carbon number of two alkyl groups couple | bonded with a benzene ring is 14-30, there will be no limitation in particular about the carbon number of each alkyl group, but carbon number of each alkyl group shall be 6-18, respectively. Is preferred.

  Furthermore, the monoalkylbenzene sulfonic acid preferably used in the present invention has one or more alkyl groups bonded to the benzene ring having 15 or more carbon atoms as described above. When the carbon number of the alkyl group bonded to the benzene ring is less than 15, the storage stability of the obtained rust preventive oil composition tends to be lowered. Further, the alkyl group bonded to the benzene ring may be linear or branched as long as the carbon number is 15 or more.

Specific examples of the sulfonate obtained using the above raw materials include the following. That is,
Alkali metal bases (alkali metal oxides, hydroxides, etc.), alkaline earth metal bases (alkali earth metal oxides, hydroxides, etc.) or amines (ammonia, alkylamines, alkanolamines, etc.) Neutral (normal salt) sulfonates obtained by reacting with sulfonic acids;
A basic sulfonate obtained by heating the neutral (normal salt) sulfonate and an excess of an alkali metal base, an alkaline earth metal base or an amine in the presence of water;
Carbonate overbased (superbasic) sulfonate obtained by reacting the neutral (normal salt) sulfonate with an alkali metal base, alkaline earth metal base or amine in the presence of carbon dioxide;
Reaction of the neutral (normal salt) sulfonate with an alkali metal base, an alkaline earth metal base or amine, and a boric acid compound such as boric acid or boric anhydride, or the carbonate overbasing (superbase) A borate overbased (superbasic) sulfonate obtained by a reaction between a sulfonate and a boric acid compound such as boric acid or boric anhydride, and a mixture thereof.

  In addition, when producing the neutral (normal salt) sulfonate, the same alkali metal, alkaline earth metal or amine chloride as the target sulfonate as a reaction accelerator is added, After preparing a neutral (normal salt) sulfonate of a different alkali metal, alkaline earth metal or amine, the same alkali metal alkaline earth metal or amine chloride as the target sulfonate is added to carry out an exchange reaction. It is also possible to obtain the desired sulfonate. However, chloride ions are likely to remain in the sulfonate obtained by such a method. Therefore, in the present invention, the sulfonate obtained by such a method is not used, or the sulfonate obtained. It is preferable to perform sufficient washing treatment such as washing with water. Specifically, the chlorine concentration in the sulfonate is preferably 200 ppm by mass or less, more preferably 100 ppm by mass or less, preferably 50 ppm by mass or less, and 25 ppm by mass or less. It is particularly preferred.

Dialkylnaphthalene sulfonates in which the total number of carbon atoms of the two alkyl groups bonded to the naphthalene ring is 14 to 30;
Two alkyl groups bonded to the benzene ring are each a branched alkyl group having one linear alkyl group or one side chain methyl group, and a dialkylbenzene sulfone having a total carbon number of 14 to 30 of the two alkyl groups Acid salts; and monoalkylbenzenesulfonates in which the number of carbon atoms of the alkyl bonded to the benzene ring is 15 or more,
It is preferable to use at least one selected from the group consisting of

  In the present invention, among the above, it is more preferable to use one or more selected from neutral, basic and overbased alkali metal sulfonates and alkaline earth metal sulfonates; base number of 0 to 50 mgKOH / G, preferably 10 to 30 mg KOH / g of neutral or near neutral alkali metal sulfonate or alkaline earth metal sulfonate and / or base number of 50 to 500 mg KOH / g, preferably 200 to 400 mg KOH / g (excess) Particular preference is given to using basic alkali metal sulfonates or alkaline earth metal sulfonates. The content of the alkali metal sulfonate or alkaline earth metal sulfonate having a base number of 0 to 50 mgKOH / g is preferably 0.1 to 15% by mass, more preferably 2 to 12% by mass based on the total amount of the composition. is there. In addition, the mass ratio of the alkali metal sulfonate or alkaline earth metal sulfonate having a base number of 0 to 50 mgKOH / g to the alkali metal sulfonate or alkaline earth metal sulfonate having a base number of 50 to 500 mgKOH / g (the base number is 0). -50 mg KOH / g alkali metal sulfonate or alkaline earth metal sulfonate / base number 50-500 mg KOH / g alkali metal sulfonate or alkaline earth metal sulfonate) is preferably 0.1-30, more preferably 1-20. Especially preferably, it is 1.5-15. Here, examples of the alkali metal include sodium and potassium, and examples of the alkaline earth metal include barium, calcium and magnesium. Calcium and magnesium are preferable, and calcium is particularly preferable. In addition, the base number as used herein refers to a JIS K 2501 “Petroleum Products and Lubricating Oils—Neutralization Number Test Method” in a state containing 30 to 70% by mass of a diluent such as a lubricating base oil. Means the base number measured by the hydrochloric acid method in accordance with

  Examples of the carboxylate include alkali metal salts, alkaline earth metal salts, and amine salts of carboxylic acids. Examples of the alkali metal, alkaline earth metal and amine constituting the carboxylate include the alkali metal, alkaline earth metal and amine exemplified in the description of the oxidized wax salt. Barium salt may be insufficiently safe for the human body and ecosystem.

  Carboxylic acid salts can be used in combination with other rust inhibitors, but when an oxidized wax salt and a lanolin fatty acid salt are used in combination with a sulfonic acid sodium salt, sodium salts are used as the oxidized wax salt and the lanolin fatty acid salt, respectively. It is preferable.

  Examples of the esters include partial esters of polyhydric alcohols, esterified oxidized waxes, esterified lanolin fatty acids, alkyl or alkenyl succinic acid esters, and the like.

  The partial ester of a polyhydric alcohol is an ester in which at least one of the hydroxyl groups in the polyhydric alcohol is not esterified and remains as a hydroxyl group, and any polyhydric alcohol as a raw material thereof can be used. Can be used, but the number of hydroxyl groups in the molecule is preferably 2 to 10 (more preferably 3 to 6) and the number of carbon atoms is 2 to 20 (more preferably 3 to 10). Alcohol is preferably used. Among these polyhydric alcohols, it is preferable to use at least one polyhydric alcohol selected from the group consisting of glycerin, trimethylolethane, trimethylolpropane, pentaerythritol and sorbitan, and it is more preferable to use pentaerythritol.

  On the other hand, as the carboxylic acid constituting the partial ester, an arbitrary one is used, and the carbon number of the carboxylic acid is preferably 2 to 30, more preferably 6 to 24, and still more preferably 10 to 22. The carboxylic acid may be a saturated carboxylic acid or an unsaturated carboxylic acid, and may be a linear carboxylic acid or a branched carboxylic acid. Such fatty acids include acetic acid, propionic acid, butanoic acid (including all isomers), pentanoic acid (including all isomers), hexanoic acid (including all isomers), heptanoic acid (all Isomers), octanoic acid (including all isomers), nonanoic acid (including all isomers), decanoic acid (including all isomers), undecanoic acid (including all isomers), Dodecanoic acid (including all isomers), tridecanoic acid (including all isomers), tetradecanoic acid (including all isomers), pentadecanoic acid (including all isomers), hexadecanoic acid (all isomers) ), Heptadecanoic acid (including all isomers), octadecanoic acid (including all isomers), nonadecanoic acid (including all isomers), icosanoic acid (including all isomers), heicossan Acid (all ), Docosanoic acid (including all isomers), tricosanoic acid (including all isomers), tetracosanoic acid (including all isomers), pentacosanoic acid (including all isomers), Hexacosanoic acid (including all isomers), heptacosanoic acid (including all isomers), octacosanoic acid (including all isomers), nonacosanoic acid (including all isomers), triacontanoic acid (all Saturated fatty acids (including isomers) (these saturated fatty acids may be linear or branched); propenoic acid, butenoic acid (including all isomers), heptenoic acid, hexenoic acid, heptenoic acid (all Isomers), octenoic acid (including all isomers), nonenoic acid (including all isomers), decenoic acid (including all isomers), undecenoic acid (including all isomers), Dodecenoic acid (all ), Tridecenoic acid (including all isomers), tetradecenoic acid (including all isomers), pentadecenoic acid (including all isomers), hexadecenoic acid (including all isomers), Heptadecenoic acid (including all isomers), octadecenoic acid (including all isomers), nonadecenoic acid (including all isomers), icosenoic acid (including all isomers), heicosenoic acid (all isomers) ), Docosenoic acid (including all isomers), tricosenoic acid (including all isomers), tetracosenoic acid (including all isomers), pentacosenoic acid (including all isomers), hexacosene Acid (including all isomers), Heptacosenic acid (including all isomers), Octacosenic acid (including all isomers), Nonacenoic acid (including all isomers), Triacontenoic acid (all Unsaturated fatty acids), and mixtures thereof.

  Moreover, you may use hydroxycarboxylic acid as carboxylic acid which comprises partial ester. The “hydroxycarboxylic acid” in the present invention means a carboxylic acid having a hydroxyl group in addition to the hydroxyl group contained in the carboxylic acid group (—COOH).

  The hydroxycarboxylic acid may be a saturated carboxylic acid or an unsaturated carboxylic acid, but is preferably a saturated carboxylic acid from the viewpoint of stability. Further, the hydroxycarboxylic acid may be a linear carboxylic acid or a branched carboxylic acid, but the linear carboxylic acid or 1 to 2 branched chains having 1 or 2 carbon atoms (more preferably 1 carbon atoms) ( More preferably, it is a branched carboxylic acid having 1 to 2, particularly preferably 1).

  Moreover, the number of carbon atoms of the hydroxycarboxylic acid is preferably 2 to 40, more preferably 6 to 30, and more preferably 8 to 24 from the viewpoint of achieving both rust prevention properties and storage stability. Further preferred.

  The number of carboxylic acid groups that the hydroxycarboxylic acid has is not particularly limited, and may be either the hydroxycarboxylic acid monobasic acid or the polybasic acid, but is preferably a monobasic acid.

  In addition, the number of hydroxyl groups that the hydroxycarboxylic acid has is not particularly limited, but is preferably 1 to 4, more preferably 1 to 3, more preferably 1 to 2 from the viewpoint of stability. Is more preferable and one is particularly preferable.

  Further, the bonding position of the hydroxyl group in the hydroxycarboxylic acid is arbitrary, but the carboxylic acid in which the hydroxyl group is bonded to the bonding carbon atom of the carboxylic acid group (α-hydroxy acid), and the main chain as viewed from the bonding carbon atom of the carboxylic acid group. A carboxylic acid having a hydroxyl group bonded to the carbon atom at the other end (ω-hydroxy acid) is preferred.

  Preferable examples of the hydroxycarboxylic acid include α-hydroxy acid represented by the following general formula (1) and ω-hydroxy acid represented by the following general formula (2).

[Wherein, R ¹ represents a hydrogen atom, an alkyl group having 1 to 38 carbon atoms, or an alkenyl group having 2 to 38 carbon atoms. ]

[Wherein, R ² represents a hydrogen atom, an alkylene group having 1 to 38 carbon atoms, or an alkenylene group having 2 to 38 carbon atoms. ]
In the general formula (1), R ¹ represents a hydrogen atom, an alkyl group having 1 to 38 carbon atoms, or an alkenyl group having 1 to 38 carbon atoms. Specific examples of the alkyl group and alkenyl group represented by R ¹ include methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, and undecyl. , Dodecyl group, tridecyl group, tetradecyl group, pentadecyl group, hexadecyl group, heptadecyl group, octadecyl group, nonadecyl group, icosyl group, heicosyl group, docosyl group, tricosyl group, tetracosyl group, pentacosyl group, hexacosyl group, heptacosyl group, octacosyl Group, nonacosyl group, triacontyl group, hentriacontyl group, dotriacontyl group, tritriacontyl group, tetratriacontyl group, pentatriacontyl group, hexatriacontyl group, heptatriacontyl group, octatriacontyl group Alkyl etc. Group (including all isomers): ethenyl group (vinyl group), propenyl group (allyl group), butenyl group, pentenyl group, hexenyl group, heptenyl group, octenyl group, nonenyl group, decenyl group, undecenyl group, dodecenyl group , Tridecenyl group, tetradecenyl group, pentadecenyl group, hexadecenyl group, heptadecenyl group, octadecenyl group, nonadecenyl group, icocenyl group, henicosenyl group, dococenyl group, tricosenyl group, tetracocenyl group, pentacocenyl group, hexacocenyl group, heptacocenyl group, heptacocenyl group, heptacocenyl group, heptacocenyl group Group, triacontenyl group, hentriacontenyl group, dotriacontenyl group, tritriacontenyl group, tetratriacontenyl group, pentatriacontenyl group, hexatriacontenyl group, heptatri Konteniru group, (including all isomers) alkenyl groups such as octa thoria Conte sulfonyl group and the like.

In the general formula (2), R ² represents a hydrogen atom, an alkylene group having 1 to 38 carbon atoms, or an alkenylene group having 2 to 38 carbon atoms. Specific examples of the alkylene group and alkenylene group represented by R ² include a methylene group, an ethylene group, a propylene group, a butylene group, a pentylene group, a hexylene group, a heptylene group, an octylene group, a nonylene group, a decylene group, and an undecylene group. , Dodecylene group, tridecylene group, tetradecylene group, pentadecylene group, hexadecylene group, heptadecylene group, octadecylene group, nonadecylene group, icosylene group, heicosylene group, docosylene group, tricosylene group, tetracosylene group, pentacosylene group, hexacosylene group, heptacene group Group, octacosylene group, nonacosylene group, triacontylene group, hentriacontylene group, dotriacontylene group, tritriacontylene group, tetratriacontylene group, pentatriacontylene group, hexato Alkylene groups (including all isomers) such as rear contylene group, heptatria acetylene group, octatria contylene group; ethenylene group (vinylene group), propenyl group (arylene group), butenylene group, pentenylene group, hexenylene group, Heptenylene group, octenylene group, nonenylene group, decenylene group, undecenylene group, dodecenylene group, tridecenylene group, tetradecenylene group, pentadecenylene group, hexadecenylene group, heptadecenylene group, octadecenylene group, nonadecenylene group, icocenylene group, icocenylene group, Tetracosenylene group, Pentacosenylene group, Hexacosenylene group, Heptacosenylene group, Octacocenylene group, Nonacosenylene group, Triacontenylene group, Hentriaconte Alkenylene groups such as Len, Dotria Contenylene, Tritria Contenylene, Tetratria Contenylene, Pentatria Contenylene, Hexatria Contenylene, Heptatria Contenylene, Octatria Contenylene, etc. (all Isomers) and the like.

  As a raw material containing such a hydroxycarboxylic acid, a lanolin fatty acid obtained by purifying (hydrolyzing etc.) a waxy substance adhering to sheep wool can be preferably used.

  When hydroxycarboxylic acid is used as the constituent carboxylic acid of the partial ester, a carboxylic acid having no hydroxyl group may be used in combination. The “carboxylic acid having no hydroxyl group” in the present invention means a carboxylic acid having no hydroxyl group other than the hydroxyl group contained in the carboxylic acid group (—COOH).

  In addition, when the carboxylic acid which comprises partial ester contains both the hydroxycarboxylic acid and the carboxylic acid which does not have a hydroxyl group, it is preferable that the ratio of the hydroxycarboxylic acid to the whole quantity of constituent carboxylic acid is 5-80 mass%. . When the proportion of hydroxycarboxylic acid is less than 5% by mass, the rust prevention property tends to be insufficient. For the same reason, the hydroxycarboxylic acid ratio is more preferably 10% by mass or more, and further preferably 15% by mass or more. Moreover, when the ratio of the said hydroxycarboxylic acid exceeds 80 mass%, it exists in the tendency for storage stability and the solubility with respect to base oil to become inadequate. For the same reason, the proportion of the hydroxycarboxylic acid is more preferably 60% by mass or less, further preferably 40% by mass or less, still more preferably 30% by mass or less, and 20% by mass or less. It is particularly preferred that

  The carboxylic acid having no hydroxyl group may be a saturated carboxylic acid or an unsaturated carboxylic acid.

  Of the carboxylic acids having no hydroxyl group, the saturated carboxylic acid may be either a straight-chain carboxylic acid or a branched carboxylic acid, but the straight-chain carboxylic acid or 1 or 2 carbon atoms (more preferably 1 carbon atom). A branched carboxylic acid having 1 to 3 (more preferably 1 to 2 and still more preferably 1) branched chains is preferable.

  The number of carbon atoms of the saturated carboxylic acid having no hydroxyl group is preferably 2 to 40, more preferably 6 to 30, and more preferably 8 to 24 from the viewpoint of achieving both rust prevention and storage stability. More preferably it is.

  The number of carboxylic acid groups in the saturated carboxylic acid having no hydroxyl group is not particularly limited and may be either a monobasic acid or a polybasic acid, but is preferably a monobasic acid.

  Among saturated carboxylic acids having no hydroxyl group, linear saturated carboxylic acids having 10 to 16 carbon atoms such as lauric acid and stearic acid are particularly preferable from the viewpoint of oxidation stability and stain resistance.

  Of the carboxylic acids having no hydroxyl group, the unsaturated carboxylic acid may be either a straight-chain carboxylic acid or a branched carboxylic acid, or a straight-chain carboxylic acid, or 1 or 2 carbon atoms (more preferably 1 carbon atoms). ) Is preferably a branched carboxylic acid having 1 to 3 (more preferably 1 to 2 and even more preferably 1) branched chains.

  Moreover, among the carboxylic acids having no hydroxyl group, the number of carbon atoms of the unsaturated carboxylic acid is preferably 2 to 40, and preferably 6 to 30 in terms of both rust prevention and storage stability. Is more preferable, it is still more preferable that it is 8-24, and it is especially preferable that it is 12-22.

  The number of carboxylic acid groups in the unsaturated carboxylic acid having no hydroxyl group is not particularly limited and may be either a monobasic acid or a polybasic acid, but is preferably a monobasic acid.

  The number of unsaturated bonds of the unsaturated carboxylic acid having no hydroxyl group is not particularly limited, but is preferably 1 to 4, more preferably 1 to 3, from the viewpoint of stability. More preferably, it is ˜2 and particularly preferably 1.

  Among unsaturated carboxylic acids having no hydroxyl group, linear unsaturated carboxylic acids having 18 to 22 carbon atoms such as oleic acid are preferable from the viewpoint of rust prevention and solubility in base oil, and oxidation stability, From the viewpoint of solubility in base oil and stain resistance, branched unsaturated carboxylic acids having 18 to 22 carbon atoms such as isostearic acid are preferable, and oleic acid is particularly preferable.

  In the partial ester of polyhydric alcohol and carboxylic acid, the proportion of unsaturated carboxylic acid in the constituent carboxylic acid is preferably 5 to 95% by mass. By making the ratio of unsaturated carboxylic acid 5 mass% or more, rust prevention property and storage stability can further be improved. For the same reason, the proportion of the unsaturated carboxylic acid is more preferably 10% by mass or more, further preferably 20% by mass or more, further preferably 30% by mass or more, and 35% by mass. The above is particularly preferable. On the other hand, when the ratio of the unsaturated carboxylic acid exceeds 95% by mass, the air exposure property and the solubility in base oil tend to be insufficient. For the same reason, the proportion of the unsaturated carboxylic acid is more preferably 80% by mass or less, still more preferably 60% by mass or less, and particularly preferably 50% by mass or less.

  The “unsaturated carboxylic acid” includes both unsaturated carboxylic acids having a hydroxyl group and unsaturated carboxylic acids having no hydroxyl group, but unsaturated carboxylic acids having no hydroxyl group in the total amount of unsaturated carboxylic acids. The ratio of the acid is preferably 80% by mass or more, more preferably 90% by mass or more, and further preferably 95% by mass or more.

  When the partial ester is a partial ester in which the proportion of the unsaturated carboxylic acid in the constituent carboxylic acid is 5 to 95% by mass, the iodine value of the partial ester is preferably 5 to 75. More preferably, it is -60, and it is still more preferable that it is 20-45. When the iodine value of the partial ester is less than 5, rust prevention properties and storage stability tend to be lowered. Moreover, when the iodine value of a partial ester exceeds 75, it exists in the tendency for the air exposure property and the solubility with respect to a base oil to fall.

  The “iodine value” as used in the present invention means an iodine value measured by an indicator titration method of JIS K 0070 “acid value, saponification value, iodine value, hydroxyl value and unsaponified product value of chemical products”. .

Examples of the method for producing a partial ester preferably used in the present invention include the following production methods (i), (ii), and (iii).
(I) Partial ester of polyhydric alcohol and hydroxycarboxylic acid (or a mixture of hydroxycarboxylic acid and saturated carboxylic acid having no hydroxyl group) and unsaturated carboxylic acid (or hydroxyl group) having no polyhydric alcohol and hydroxyl group And a partial ester of a mixture of an unsaturated carboxylic acid having no carboxylic acid and a saturated carboxylic acid having no hydroxyl group) are mixed so that the carboxylic acid composition in the mixture of the two satisfies the above conditions.
(Ii) A carboxylic acid having a hydroxyl group and an unsaturated carboxylic acid having no hydroxyl group are mixed so that the carboxylic acid composition of the resulting partial ester satisfies the above conditions (or a saturated carboxylic acid having no hydroxyl group is mixed). Further mixing), a partial esterification reaction between the carboxylic acid mixture and the polyhydric alcohol is performed.
(Iii) A partial ester of a mixture of a hydroxycarboxylic acid and an unsaturated carboxylic acid having no hydroxyl group (or a mixture of these carboxylic acid and a saturated carboxylic acid having no hydroxyl group) has a carboxylic acid composition as described above. A partial ester of a polyhydric alcohol and a hydroxycarboxylic acid (or a mixture of a hydroxycarboxylic acid and a saturated carboxylic acid having no hydroxyl group) or an unsaturated carboxylic acid having no polyhydric alcohol and a hydroxyl group so as to satisfy the conditions A partial ester of (or a mixture of an unsaturated carboxylic acid having no hydroxyl group and a saturated carboxylic acid having no hydroxyl group) is mixed.

  For example, in the case of the production method (i), a lanolin fatty acid is used as a mixture of a hydroxycarboxylic acid and a saturated carboxylic acid having no hydroxyl group, and an unsaturated carboxylic acid having no hydroxyl group is an carboxylic acid having 2 to 40 carbon atoms. Unsaturated carboxylic acids can be preferably used. In this case, a partial ester (first partial ester) composed of a mixture of polyhydric alcohol, hydroxycarboxylic acid and saturated carboxylic acid having no hydroxyl group (preferably lanolin fatty acid), polyhydric alcohol and hydroxyl group The content ratio of the partial ester (second partial ester) composed of the unsaturated carboxylic acid (preferably oleic acid) that is not present is not particularly limited as long as the carboxylic acid composition ratio in the mixture satisfies the above conditions. However, the ratio of the first partial ester to the total amount of the first and second partial esters is preferably 20 to 95% by mass, more preferably 40 to 80% by mass, and 55 to 65%. It is particularly preferable that the content is mass%. When the ratio of the first partial ester is less than 20% by mass or exceeds 95% by mass, rust prevention properties such as air exposure tend to be insufficient. Moreover, when the ratio of 1st partial ester exceeds 95 mass%, the solubility with respect to the base oil of the whole partial ester will fall, and it exists in the tendency for storage stability to become inadequate.

  The esterified oxidized wax refers to a product obtained by reacting an oxidized wax with an alcohol to esterify part or all of the acidic groups of the oxidized wax. Here, as the oxidized wax used as the raw material of the esterified oxidized wax, the oxidized wax exemplified in the description of the oxidized wax salt; the alcohols are linear or branched having 1 to 20 carbon atoms. Examples thereof include saturated monohydric alcohols, linear or branched unsaturated monohydric alcohols having 1 to 20 carbon atoms, polyhydric alcohols exemplified in the description of the ester, alcohols obtained by hydrolysis of lanolin, and the like. .

  The esterified lanolin fatty acid refers to a product obtained by reacting a lanolin fatty acid obtained by purifying (hydrolyzing, etc.) a waxy substance adhering to sheep wool and an alcohol. Here, examples of the alcohol used as a raw material for the esterified lanolin fatty acid include alcohols exemplified in the description of the esterified oxidized wax, and among them, polyhydric alcohols are preferable, and trimethylolpropane, trimethylolethane, and sorbitan. , Pentaerythritol and glycerin are more preferable.

  Examples of the alkyl or alkenyl succinic acid ester include esters of the above-described alkyl or alkenyl succinic acid with a monohydric alcohol or a dihydric or higher polyhydric alcohol. Among these, esters of monohydric alcohols and dihydric alcohols are preferable.

  The monohydric alcohol here may be a linear or branched one, and may be a saturated alcohol or an unsaturated alcohol. Moreover, although carbon number in particular of monohydric alcohol is not restrict | limited, C8-C18 aliphatic alcohol is used preferably.

  As the dihydric alcohol, alkylene glycol and polyoxyalkylene glycol are preferably used. Specific examples of the alkylene glycol include ethylene glycol, propylene glycol, butylene glycol, pentylene glycol, hexylene glycol, heptylene glycol, octylene glycol, nonylene glycol, and decylene glycol. Examples of the polyoxyalkylene glycol include those obtained by homopolymerization or copolymerization of a certain group side such as ethylene oxide, propylene oxide, butylene oxide. In the polyoxyalkylene glycol, when alkylene oxides having different structures are copolymerized, the polymerization form of the oxyalkylene group is not particularly limited, and may be random copolymerization or block copolymerization. Moreover, the polymerization degree of polyoxyalkylene glycol is not particularly limited, but is preferably 2 to 10, more preferably 2 to 8, and still more preferably 2 to 6.

  The alkyl or alkenyl succinic acid ester may be a diester in which both of two —COOH groups of the alkyl or alkenyl succinic acid are esterified (complete ester), or only one of the —COOH groups is an ester. Monoester (partial ester) may be used, but monoester is preferable from the viewpoint of more excellent rust prevention.

Moreover, as sarcosine, the compound represented by either of the following general formula (3)-(5) is used preferably. By including the sarcosine represented by the general formulas (3) to (5) in the rust preventive oil composition of the present invention, rust preventive properties can be obtained without using heavy components such as wax, petrolatum, and heavy base oil. In addition, the anti-corrosion property can be maintained at a high level over a long period of time, so that the anti-corrosion property and the long-term maintainability are excellent, and the increase in the amount taken out is suppressed and the degreasing is performed. It is possible to obtain a rust-preventing oil composition advantageous in terms of water and sprayability.
R ³ —CO—NR ⁴ — (CH ₂ ) _n —COOX (3)
(In the formula, R ³ is an alkyl group having 6 to 30 carbon atoms or an alkenyl group having 6 to 30 carbon atoms, R ⁴ is an alkyl group having 1 to ⁴ carbon atoms, X is a hydrogen atom, and an alkyl group having 1 to 30 carbon atoms. Or an alkenyl group having 1 to 30 carbon atoms, and n represents an integer of 1 to 4.)
_{^{[R 3 -CO-NR 4 -}} (CH 2) n -COO] m Y (4)
Wherein R ³ is an alkyl group having 6 to 30 carbon atoms or an alkenyl group having 6 to 30 carbon atoms, R ⁴ is an alkyl group having 1 to ⁴ carbon atoms, Y is an alkali metal or alkaline earth metal, and n is 1 An integer of ˜4, m is 1 when Y is an alkali metal, and 2 when Y is an alkaline earth metal.
_{^{[R 3 -CO-NR 4 -}} (CH 2) n -COO] m -Z- (OH) m '(5)
(Wherein R ³ is an alkyl group having 6 to 30 carbon atoms or an alkenyl group having 6 to 30 carbon atoms, R ⁴ is an alkyl group having 1 to ⁴ carbon atoms, and Z is a hydroxyl group of a polyhydric alcohol having 2 or more valences) And m represents an integer of 1 or more, m ′ represents an integer of 0 or more, m + m ′ represents a valence of Z, and n represents an integer of 1 to 4.)
In general formulas (3) to (5), R ³ represents an alkyl group having 6 to 30 carbon atoms or an alkenyl group having 6 to 30 carbon atoms. From the viewpoint of solubility in base oil, the alkyl group or alkenyl group must have 6 or more carbon atoms, preferably 7 or more carbon atoms, and more preferably 8 or more carbon atoms. Further, from the viewpoint of storage stability and the like, it is necessary that the alkyl group or alkenyl group has 30 or less carbon atoms, preferably 24 or less carbon atoms, and more preferably 20 or less carbon atoms. Specific examples of such alkyl groups and alkenyl groups include hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, Alkyl groups such as heptadecyl group, octadecyl group, nonadecyl group, icosyl group (these alkyl groups may be linear or branched); hexenyl group, heptenyl group, octenyl group, nonenyl group, decenyl group, undecenyl group, dodecenyl group Group, tridecenyl group, tetradecenyl group, pentadecenyl group, hexadecenyl group, heptadecenyl group, octadecenyl group, nonadecenyl group, icocenyl group and the like alkenyl groups (these alkenyl groups may be linear or branched, and the position of the double bond) Are also optional)

In general formulas (3) to (5), R ⁴ represents an alkyl group having 1 to ⁴ carbon atoms. From the viewpoint of storage stability and the like, it is necessary that the alkyl group has 4 or less carbon atoms, preferably 3 or less carbon atoms, and more preferably 2 or less carbon atoms. In general formulas (3) to (5), n represents an integer of 1 to 4. From the viewpoint of storage stability and the like, it is necessary to be an integer of 4 or less, preferably 3 or less, and more preferably 2 or less.

  In General Formula (3), X represents a hydrogen atom, an alkyl group having 1 to 30 carbon atoms, or an alkenyl group having 1 to 30 carbon atoms. The alkyl group or alkenyl group represented by X needs to have 30 or less carbon atoms from the viewpoint of storage stability, preferably 20 or less carbon atoms, and preferably 10 or less carbon atoms. More preferred. Specific examples of such an alkyl group or alkenyl group include alkyl groups such as a methyl group, an ethyl group, a propyl group, a butyl group, a pentyl group, a hexyl group, a heptyl group, an octyl group, a nonyl group, and a decyl group. (These alkyl groups may be linear or branched); alkenyl groups such as ethenyl group, propenyl group, butenyl group, pentenyl group, hexenyl group, heptenyl group, octenyl group, nonenyl group, decenyl group (these alkenyl groups) May be linear or branched, and the position of the double bond is arbitrary). Moreover, it is preferable that it is an alkyl group from the point of being excellent in rust prevention property. X is preferably a hydrogen atom, an alkyl group having 1 to 20 carbon atoms, or an alkenyl group having 1 to 20 carbon atoms from the viewpoint of more excellent rust-preventing properties, and is preferably a hydrogen atom or 1 to 20 carbon atoms. It is more preferably an alkyl group, and even more preferably a hydrogen atom or an alkyl group having 1 to 10 carbon atoms.

  In the general formula (4), Y represents an alkali metal or an alkaline earth metal, and specific examples include sodium, potassium, magnesium, calcium, barium and the like. Among these, alkaline earth metals are preferable because they are more excellent in rust prevention. In addition, in the case of barium, there is a risk that the safety to the human body and the ecosystem will be insufficient. In the general formula (3), m represents 1 when Y is an alkali metal, and 2 when Y is an alkaline earth metal.

  In general formula (5), Z represents the residue except the hydroxyl group of the polyhydric alcohol more than bivalence. Specific examples of such polyhydric alcohols include ethylene glycol, propylene glycol, 1,4-butanediol, 1,2-butanediol, neopentyl glycol, 1,6-hexanediol, 1,2- Octanediol, 1,8-octanediol, isoprene glycol, 3-methyl-1,5-pentanediol, sorbite, catechol, resorcin, hydroquinone, bisphenol A, bisphenol F, hydrogenated bisphenol A, hydrogenated bisphenol F, dimer diol Divalent alcohols such as glycerin, 2- (hydroxymethyl) -1,3-propanediol, 1,2,3-butanetriol, 1,2,3-pentanetriol, 2-methyl-1,2,3 -Propanetriol, 2-methyl-2,3,4- Tantriol, 2-ethyl-1,2,3-butanetriol, 2,3,4-pentanetriol, 2,3,4-hexanetriol, 4-propyl-3,4,5-heptanetriol, 2,4 -Trihydric alcohols such as dimethyl-2,3,4-pentanetriol, 1,2,4-butanetriol, 1,2,4-pentanetriol, trimethylolethane, trimethylolpropane; pentaerythritol, erythritol, 1, 2,3,4-pentanetetrol, 2,3,4,5-hexanetetrol, 1,2,4,5-pentanetetrol, 1,3,4,5-hexanetetrol, diglycerin, sorbitan Tetrahydric alcohols such as adonitol, arabitol, xylitol, triglycerin, etc .; dipentaerythritol Le, sorbitol, mannitol, iditol, inositol, dulcitol, talose, hexavalent alcohols such as allose, polyglycerin or their dehydrated condensates and the like.

  In the general formula (5), m is an integer of 1 or more, m ′ is an integer of 0 or more, and m + m ′ is the same as the valence of Z. That is, all of the hydroxyl groups of the polyhydric alcohol of Z may be substituted, or only a part thereof may be substituted.

  Among the sarcosine represented by the general formulas (3) to (5), the sarcosine is at least one compound selected from the general formulas (3) and (4) from the viewpoint of more excellent anti-rust properties. preferable. Moreover, only 1 type of compound chosen from general formula (3)-(5) may be used independently, and the mixture of 2 or more types of compounds may be used.

  Examples of the amine include amines exemplified in the description of the oxidized wax salt.

  In addition, examples of the boron compound include calcium borate.

  Further, in addition to the above rust inhibitor, alcohols represented by higher aliphatic alcohols; phosphoric acid monoesters, phosphoric acid diesters, phosphorous esters, (amine) phosphorus represented by amine salts thereof Acid derivatives and the like can also be included as rust inhibitors.

  In producing the above rust inhibitor, a chlorine bleach may be used for the purpose of decolorization. In the present invention, a specific chlorine compound such as hydrogen peroxide is used as a bleach. Alternatively, it is preferable not to perform the decoloring process. In addition, chlorine compounds such as hydrochloric acid may be used for the hydrolysis of fats and oils. In this case, it is also preferable to use a non-chlorine acid or basic compound. Furthermore, it is preferable to subject the resulting compound to a sufficient washing treatment such as washing with water.

  Further, the chlorine concentration of the rust preventive additive is not particularly limited as long as the characteristics of the rust preventive oil composition are not impaired, but is preferably 200 ppm by mass or less, more preferably 100 ppm by mass or less. Yes, more preferably 50 ppm or less, particularly preferably 25 ppm by mass or less.

  In the rust preventive oil composition of the present invention, one of the rust preventive additives may be used alone, or two or more may be mixed and used. However, in the rust preventive oil composition of the present invention containing carboxylic acid as an essential component, it is preferable to use a sulfonate because higher rust preventive properties can be obtained. Furthermore, when using a sulfonate, you may further contain at least 1 sort (s) chosen from carboxylate, ester, sarcosine, an amine, and a boron compound. Furthermore, the rust inhibitor used in combination with the sulfonate is preferably at least one selected from esters and carboxylates, and more preferably used in combination with esters and carboxylates. In addition, as the ester herein, a partial ester of polyhydric alcohol and a partial ester of alkenyl succinic acid are preferable. As the carboxylic acid, fatty acid, dimer acid and alkenyl succinic acid are preferable. As the carboxylate, a fatty acid salt and Lanolin fatty acid salts are preferred.

  In the rust prevention composition of the present invention, the content of rust prevention additives other than oxidized wax and carboxylic acid is preferably 0.1 to 40% by mass, more preferably 0.5 to 30% by mass, and still more preferably 1. ˜20 mass%. When the content of the rust prevention additive is less than the lower limit, the effect of improving the rust prevention property due to the addition tends to be insufficient. Moreover, even if content of the said rust prevention additive exceeds 40 mass%, it exists in the tendency for the improvement effect of the rust prevention property corresponding to content not to be acquired.

  Moreover, in the rust prevention oil composition of this invention, you may contain another additive as needed. Here, specific examples of other additives used in the present invention include, for example, paraffin wax having a remarkable effect of improving the rust-preventing property in an acidic atmosphere; Fats and oils, sulfurized esters, phosphate esters such as long-chain alkyl zinc dithiophosphates, tricresyl phosphates, fats and oils such as pork fats, fatty acids, higher alcohols, calcium carbonate, potassium borate; phenols to improve antioxidant performance Or amine antioxidants; corrosion inhibitors (benzotriazole or derivatives thereof, thiadiazole, benzothiazole, etc.) for improving corrosion prevention performance; wetting agents such as diethylene glycol monoalkyl ether; acrylic polymers, paraffin wax, microwax , Slack wack , Polyolefin waxes, film-forming agents such as petrolatum; methyl silicone, fluorosilicone, antifoaming agents such as polyacrylates, water-soluble spoilage factors water and surfactant to remove, and mixtures thereof. In addition, although content of said other additive is arbitrary, it is preferable that the sum total of content of these additives is 10 mass% or less on the basis of rust prevention oil composition whole quantity.

  Further, in the rust preventive oil composition of the present invention, the barium, zinc, chlorine and lead contents are each converted to elements, preferably 1000 ppm by mass or less, more preferably 500 ppm, based on the total amount of the rust preventive oil composition. The mass ppm or less, more preferably 100 mass ppm or less, still more preferably 50 mass ppm or less, still more preferably 10 mass ppm or less, particularly preferably 5 mass ppm or less, and most preferably 1 mass ppm or less. If the content of any one of these elements exceeds 1000 ppm by mass, there is a possibility that safety to the environment such as the human body or the ecosystem is insufficient.

  In addition, content of the element in this invention means the value measured by the following method. That is, the content of barium, zinc and lead is ASTM D 5185-95 "Standard TestMethod for Determination of Additive Elements, Wear Metals, and Contaminants in Used Lubricating Oils and Determination of Selected Elements in Base Oils by Inductively Coupled Plasma Atomic Emission Spectrometry ( ICP-AES) "; chlorine content refers to the content [mass ppm] based on the total amount of the composition measured according to" IP PRPOSED METHOD AK / 81 Determination of chlorine-Microcoulometery oxidative method ", respectively. means. The detection limit of each element in the above measurement method is usually 1 mass ppm.

  Further, the base number of the rust-preventing oil composition of the present invention is not particularly limited, but from the viewpoint of rust prevention properties, the base number is preferably 1 mgKOH / g or more, more preferably 1.5 mgKOH / g or more, and still more preferably. Is 2 mgKOH / g or more, particularly preferably 3 mgKOH / g or more. From the viewpoint of storage stability, the base number is preferably 20 mgKOH / g or less, more preferably 15 mgKOH / g or less, still more preferably 10 mgKOH / g or less, and particularly preferably 8 mgKOH / g. The base number referred to here is 6. JIS K 2501 “Petroleum products and lubricants—neutralization number test method”. The base number [mgKOH / g] measured by the hydrochloric acid method according to the above.

Further, the kinematic viscosity at 40 ° C. of the rust preventive oil composition of the present invention is not particularly limited, but is preferably 1 mm ² / s or more, more preferably 2 mm ² / s or more, further preferably 2.5 mm ² / s or more, More preferably, it is 3 mm < ² > / s or more, Most preferably, it is 3.5 mm < ² > / s or more. When the kinematic viscosity at 40 ° C. of the rust-preventing oil composition is less than the lower limit value, the oil film of the coating film is likely to break, and the rust-preventing property tends to be insufficient. Moreover, the kinematic viscosity at 40 ° C. of the rust preventive oil composition of the present invention is preferably 50 mm ² / s or less, more preferably 40 mm ² / s or less, and further preferably 30 mm ² / s or less. When the kinematic viscosity at 40 ° C. of the rust preventive oil composition exceeds the upper limit, workability tends to be lowered.

Even when the viscosity of the rust preventive composition of the present invention is high, by applying the kinematic viscosity to a predetermined value or less (preferably 50 mm ² / s or less) by heating to the object to be treated, The composition can be easily and reliably applied to an object to be processed. However, when the kinematic viscosity at 40 ° C. of the rust-preventing oil composition exceeds 1000 mm ² / s, heating at a higher temperature is required to reduce the viscosity, which promotes deterioration of the rust-preventing oil. Performance will be impaired. Therefore, the kinematic viscosity at 40 ° C. of the rust preventive oil composition of the present invention is preferably 1000 mm ² / s or less.

  The rust preventive oil composition of the present invention having the above configuration can achieve all of rust preventive properties, degreasing properties and storage stability at a high level in a balanced manner, and is suitable as a rust preventive oil for various metal members. Can be used. There are no particular restrictions on the metal member that is the object to be treated. Specifically, it is a cold-rolled steel sheet, hot-rolled steel sheet, high-tensile latter half, galvanized steel sheet, etc. Examples thereof include metal plate materials such as an original plate, an aluminum alloy plate, and a magnesium alloy plate, and further bearing components such as a rolling bearing, a tapered rolling bearing, and a needle bearing, an architectural steel material, and a precision component.

  As rust prevention oil for such metal members, intermediate rust prevention oil used in the process of processing metal members, shipping rust prevention oil used for rust prevention at the time of shipment, before being subjected to press working There are cleaning rust preventive oils used in the cleaning process for removing foreign substances in the metal plate manufacturer or prior to shipping in the metal plate manufacturer, but the rust preventive oil composition of the present invention should be used for any of the above applications. Can do.

  Moreover, the method in particular of apply | coating the rust prevention oil composition of this invention to a to-be-processed object is not restrict | limited, For example, it applies to metal members by methods, such as spray, dripping, the transfer by a felt material, electrostatic oiling. be able to. Among these coating methods, the spray method is preferable because the oil film thickness can be made uniform by coating in a fine mist. The application apparatus in the case of applying the spray method is not particularly limited as long as it can atomize the rust preventive oil composition, and for example, any of an air spray type, an airless spray type, a hot melt type and the like can be applied. .

  Furthermore, in the coating process, it is preferable to provide a drain cutting process using a centrifuge or a drain cutting process by leaving for a long time after an excessive rust preventive oil composition is coated.

  Further, when the rust-preventing oil composition of the present invention is used as a cleaning rust-preventing oil composition, a large excess amount of the rust-preventing oil composition of the present invention is sprayed, showered, or dipped on the surface of a metal member. Good cleaning and subsequent rust prevention can be performed by refueling. Furthermore, if the surface cleaning with a roll brush or the like is performed after the above-described metal processing step as necessary, the efficiency of removing foreign matters can be enhanced. Furthermore, when performing cleaning using the rust preventive oil composition of the present invention, it is possible to adjust the amount of oil adhering to the surface of the metal member by performing surface treatment of the metal member with a ringer roll or the like. preferable.

  Regardless of the application method of the rust-preventing oil composition of the present invention, it is preferable to recover, circulate and reuse the rust-preventing oil composition applied in excess on the metal member. It should be noted that when the rust preventive oil composition is circulated, it is preferable to remove foreign matters mixed in the circulation system. Specifically, for example, a foreign substance can be removed by providing a filter in the course of the circulation path of the rust preventive oil composition of the present invention, preferably immediately before the rust preventive oil composition is jetted toward the metal member. it can. Moreover, a magnet can be provided in the bottom part of the tank which stores the rust prevention oil composition of this invention, and foreign matters, such as an abrasion part, can also be adsorb | sucked and removed by magnetic force. In addition, there is a concern that the performance of the rust preventive oil composition of the present invention that is reused in such a process is deteriorated due to contamination of the oil in the previous process. Therefore, when reusing the rust-preventing oil composition of the present invention, the properties are controlled by periodically measuring the kinematic viscosity and density, copper plate corrosion test, rust-preventing property test, etc. on the oil used. It is preferable to perform oil renewal, drain disposal, tank cleaning, oil purification operation, etc. as necessary. Furthermore, the discarded oil is used as it is or diluted with a solvent or a low-viscosity base oil, and used in a line where the required performance for the rust prevention oil composition is lower than the line used before disposal. As a result, the total amount of oil used can be reduced. Furthermore, when the rust preventive oil composition of the present invention is stored in a tank, it is preferably replenished according to the amount of decrease in the composition in the tank. In that case, it may not necessarily be the same composition as the rust-preventing oil composition filled in the initial stage, but a composition with an increased amount of additives for drawing out the performance to be enhanced may be replenished depending on the occasion. Alternatively, conversely, the cleaning ability of the rust-preventing oil composition may be maintained by replenishing a composition having a reduced viscosity by a method such as reducing the content of the high-viscosity base oil.

  In addition, when the rust preventive oil composition of the present invention is used in a cleaning process for removing foreign matters prior to shipment at a metal plate manufacturer, the metal plate is wound up in a coil shape immediately after the cleaning process or stacked as a sheet material. Can be shipped. That is, the rust preventive oil composition of the present invention can be used as a cleaning rust preventive oil and a shipping rust preventive oil. According to this method, there is a merit that the amount of foreign matter attached is small and cleaning can be performed easily and reliably even when a cleaning process using a cleaning rust preventive oil is performed immediately before the pressing process in pressing. As a matter of course, a rust-preventing treatment may be performed in two stages by providing a step of applying rust-preventing oil again after the step of washing with the cleaning rust-preventing oil at the steel plate manufacturing site.

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.
[Examples 1 to 5, Comparative Examples 1 and 2]
In Examples 1 to 5 and Comparative Examples 1 and 2, rust prevention oil compositions having the compositions shown in Table 1 were prepared using the base oils and additives shown below, respectively. Table 1 also shows the ratio (mass ratio) of carboxylic acid / oxidized wax salt. Table 2 shows the fatty acid composition of the lanolin fatty acid constituting the C6 partial ester.
(Base oil)
Base oil 1: mineral oil (kinematic viscosity at 30 ° C .: 2.0 mm ² / s, initial boiling point: 190 ° C., end point: 250 ° C., flash point: 80 ° C., aniline point: 72 ° C.)
Base oil 2: mineral oil (kinematic viscosity at 40 ° C .: 22 mm ² / s)
Base oil 3: mineral oil (kinematic viscosity at 40 ° C .: 480 mm ² / s)
(Oxidized wax salt)
A1: Calcium salt of oxidized wax (carboxylic acid)
B1: Dimer acid of oleic acid (other additives)
C1: di-tert-butyl-p-cresol C2: benzotriazole C3: alkylbenzene calcium sulfonate solution (sulfonate content: 52% by mass, base number: 300 mgKOH / g)
C4: 115 ° F. paraffin wax C5: sorbitan monooleate C6: partial ester of pentaerythritol and lanolin fatty acid (monoester / diester / triester = 5/10/85) and partial ester of pentaerythritol and oleic acid ( Mixture with monoester / diester / triester = 5/10/85) (partially ester of lanolin fatty acid / partial ester of oleic acid = 60/40 (mass ratio), iodine value: 31.4, component carvone of partial ester 18% by mass of the hydroxycarboxylic acid in the acid, and 46.9% by mass of the unsaturated carboxylic acid in the carboxylic acid constituting the partial ester)
C7: Alkylbenzene calcium sulfonate solution (sulfonate content: 40% by mass, base number: 25 mgKOH / g).

  Next, the following evaluation tests were performed on the rust preventive oil compositions of Examples 1 to 5 and Comparative Examples 1 and 2.

(Salt spray test)
A commercially available cold rolled steel plate corresponding to SPCE-SD was cut to 60 × 80 mm to obtain a test piece. Next, the rust-preventing oil composition was applied to the test piece using an air spray so that the coating amount was 3 g / m ^2, and left at room temperature for 24 hours. The test piece thus obtained was subjected to a salt spray test in accordance with JIS K 2246 “Salt spray test method”, and the degree of rust after 48 and 72 hours was evaluated as follows:
A: 0%
B: 1-10%
C: 11-25%
D: 26-50%
E: Evaluated based on 51% or more. The obtained results are shown in Table 1.

(Degreasing test)
A commercially available cold rolled steel plate corresponding to SPCE-SD was cut to 60 × 80 mm to obtain a test piece. Next, the rust preventive oil composition was applied to the test piece using an air spray so that the coating amount was 3 g / m ² . The test piece after application | coating was stored for 24 hours in the Hyakuba box installed outdoors. The test piece after storage was immersed for 2 minutes in an alkaline degreasing agent in which a nonionic surfactant was combined with a sodium phosphate or sodium silicate alkaline builder, and then washed in running water for 30 seconds. Thereafter, the test piece is held vertically for 20 seconds, and the degreasing property is determined by the wetted area ratio according to the following criteria:
A: 90% or more B: 90-60%
C: Evaluated based on 60% or less. The obtained results are shown in Table 1.

(Storage stability test)
30 g of sample oil was weighed in a glass bottle with a capacity of 50 ml. This sample was kept at 20 ° C. and 50% relative humidity for 12 hours, and then kept at 50 ° C. and 95% relative humidity for 12 hours as one cycle, and this cycle was continued until clouding or precipitation occurred. Repeated. From the number of days (cycles) required until cloudiness or precipitation occurs, the following criteria:
A: 10 days or more B: 7-9 days C: 4-6 days D: 2-3 days E: The storage stability of the rust preventive oil composition was evaluated on the basis of within 1 day. The obtained results are shown in Table 1.

Claims (1)

A rust-preventing oil composition comprising a base oil composed of mineral oil and / or synthetic oil, an oxidized wax salt, and a carboxylic acid.