JP2006274177A - Refrigerator oil composition - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a refrigerator oil capable of sufficiently reducing both coefficients of static friction and dynamic friction at a sliding part of a refrigerant-compressor or the like. <P>SOLUTION: The refrigerator oil composition contains a prescribed lubricant base oil and at least one kind of a nitrogen-containing oily agent selected from an amine, a carboxylic acid salt and amide of the amine. Both of starting electric power and power consumption are reduced by the refrigerator oil composition to achieve high-level energy saving because the both coefficients of the static friction and the dynamic friction at the sliding part of the refrigerant-compressor or the like can be reduced. <P>COPYRIGHT: (C)2007,JPO&INPIT

Description

  The present invention relates to a refrigerator oil composition.

  Refrigerating machine oils suitable for alternative refrigerants are being studied as refrigerant alternatives to ozone-depleting fluorocarbons based on the Montreal Protocol are being promoted.

  For example, Patent Documents 1 to 3 listed below disclose a hydrofluorocarbon (HFC) refrigerant refrigerating machine oil that uses a polyol ester or ether-based synthetic oil that is compatible with the HFC refrigerant.

In addition, as a refrigerating machine oil having improved characteristics such as frictional properties and wear resistance, the following Patent Document 4 discloses a refrigerating machine oil containing a predetermined amount of a thiadiazole compound and dibenzyl disulfide in a predetermined lubricating base oil. Has been.
Japanese National Patent Publication No. 3-505602 Japanese Patent Laid-Open No. 3-128992 JP-A-3-200955 JP 2004-67836 A

  By the way, in recent years, in the field of refrigerating and air-conditioning equipment such as air conditioners and refrigerators, interest in energy saving has been increased, and studies are being made to reduce power consumption during startup and during operation.

  Among these, as means for reducing power consumption during operation, for example, there is a method of reducing energy loss by adding a friction modifier to refrigeration oil to lower the dynamic friction coefficient in the sliding portion. From such a viewpoint, although the thiadiazole compound and the dibenzyl disulfide are used in the said patent document 4, the friction reduction effect obtained when these additives are used is not necessarily enough.

  Moreover, as means for reducing the starting power, for example, there is a method of improving the compression efficiency by operating the refrigerant compressor at low speed rotation by inverter control and reducing the energy loss. If the rotational speed of the compressor fluctuates greatly due to the change in value, the frictional force also increases accordingly. Therefore, in order to reduce the starting power, it is desirable to use a refrigerating machine oil that can reduce the coefficient of static friction, but from this point of view, studies for improving the friction characteristics of the refrigerating machine oil have not been sufficiently performed.

  The present invention has been made in view of such circumstances, and can sufficiently reduce both the static friction coefficient and the dynamic friction coefficient in the sliding portion of the refrigerant compressor or the like, thereby achieving a high level of energy saving. An object of the present invention is to provide a refrigerating machine oil that can be used.

  In order to solve the above-mentioned problems, the present invention contains a predetermined lubricating base oil and at least one nitrogen-containing oily agent selected from amines, amine carboxylates and amides. A machine oil composition is provided.

  According to the refrigerating machine oil composition of the present invention, by including a predetermined lubricating base oil and the specific nitrogen-containing oily agent, both the static friction coefficient and the dynamic friction coefficient in the sliding portion of the refrigerant compressor or the like are obtained. Since it can be sufficiently reduced, both the starting power and the power consumption during operation can be reduced, and a high level of energy saving can be achieved.

  According to the present invention, there is provided a refrigerating machine oil composition capable of sufficiently reducing both the static friction coefficient and the dynamic friction coefficient in a sliding portion such as a refrigerant compressor and achieving a high level of energy saving. The

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

  The base oil used in the present invention may be either mineral oil or synthetic oil, or may be a mixed base oil of mineral oil and synthetic oil.

  As mineral oils, for example, solvent degreasing, solvent extraction, hydrocracking of lubricating oil fractions obtained by atmospheric distillation and vacuum distillation of paraffinic, intermediate or naphthenic crude oils , Paraffinic mineral oil or naphthenic mineral oil obtained by applying a combination of one or more kinds of purification means such as solvent dewaxing, catalytic dewaxing, hydrorefining, sulfuric acid washing, and clay treatment as appropriate.

  Among these mineral oils, it is preferable to use highly refined mineral oil (hereinafter referred to as “highly refined mineral oil”) from the viewpoint of superior thermal stability. Specific examples of highly refined mineral oils include distillate oil obtained by atmospheric distillation of paraffinic crude oil, intermediate crude oil or naphthenic crude oil, or by distilling residual oil of atmospheric distillation under reduced pressure according to a conventional method. Refined oil obtained by refining; deep dewaxed oil obtained by further deep dewaxing after refining; hydrotreated oil obtained by hydrotreating, and the like.

  The purification method in the purification step is not particularly limited, and a conventionally known method can be used. For example, (a) hydrogenation treatment, (b) dewaxing treatment (solvent dewaxing or hydrodehydration). A method of performing any one of wax), (c) solvent extraction treatment, (d) alkali washing or sulfuric acid washing treatment, and (e) clay processing alone or in combination of two or more in an appropriate order. Can be mentioned. It is also effective to repeat any one of the processes (a) to (e) in a plurality of stages. More specifically, (i) a method of hydrotreating distillate oil, or a method of performing alkali washing or sulfuric acid washing treatment after hydrogenation treatment; (ii) dehydrating oil after hydrogenation treatment. A method of wax treatment; (iii) a method of subjecting the distillate to a hydrogenation treatment after solvent extraction; (iv) subjecting the distillate to a two-stage or three-stage hydrotreatment, or subsequent alkali washing or sulfuric acid (V) A method of dewaxing again to obtain a deep dewaxed oil after the above-described treatments (i) to (iv), and the like.

  Among highly refined mineral oils obtained by the above refining method, naphthenic mineral oils and mineral oils obtained by deep dewaxing are preferred from the viewpoints of low temperature fluidity and no wax precipitation at low temperatures. This deep dewaxing process is usually performed by a solvent dewaxing process under severe conditions, a catalytic dewaxing process using a zeolite catalyst, or the like.

  Further, the non-aromatic unsaturation (unsaturation) of such highly refined mineral oil is preferably 10% by mass or less, more preferably 5% by mass or less, still more preferably 1% by mass or less, and particularly preferably 0.1% by mass. % Or less. When the non-aromatic unsaturated content exceeds 10% by mass, sludge is likely to be generated, and as a result, the expansion mechanism such as a capillary constituting the refrigerant circulation system tends to be blocked.

  On the other hand, synthetic oils used in the present invention include hydrocarbon oils such as olefin polymers, naphthalene compounds, alkylbenzenes; esters, polyalkylene glycols, polyvinyl ethers, ketones, polyphenyl ethers, silicones, polysiloxanes, perfluoroethers. And other oxygen-containing synthetic oils.

  Examples of the olefin polymer include those obtained by polymerizing an olefin having 2 to 12 carbon atoms, and those obtained by hydrogenating a compound obtained by the polymerization, such as polybutene, polyisobutene, and α having 5 to 12 carbon atoms. -Oligomeric oligomers (poly-alpha olefins), ethylene-propylene copolymers, and hydrogenated products thereof are preferably used.

  The production method of the olefin polymer is not particularly limited, and can be produced by various known methods. For example, poly α-olefin is produced by using α-olefin produced from ethylene as a raw material and treating it with a known polymerization method such as Ziegler catalyst method, radical polymerization method, aluminum chloride method, boron fluoride method and the like. .

  The naphthalene compound is not particularly limited as long as it has a naphthalene skeleton, but has 1 to 4 alkyl groups having 1 to 10 carbon atoms and has a total carbon content of alkyl groups from the viewpoint of excellent compatibility with the refrigerant. Those having 1 to 10 carbon atoms are preferred, those having 1 to 3 alkyl groups having 1 to 8 carbon atoms and those having 3 to 8 carbon atoms in total are more preferred.

  Specific examples of the alkyl group having 1 to 10 carbon atoms that the naphthalene compound has include a methyl group, an ethyl group, an n-propyl group, an isopropyl group, a linear or branched butyl group, a linear or branched group. A branched pentyl group, a linear or branched hexyl group, a linear or branched heptyl group, a linear or branched octyl group, a linear or branched nonyl group, Examples thereof include a linear or branched decyl group.

  In addition, when using a naphthalene compound, the compound of a single structure may be used independently, and 2 or more types of the compounds from which a structure differs may be used in combination.

  Moreover, the manufacturing method in particular of the said naphthalene compound is not restrict | limited, It can manufacture with a various well-known method. Examples of this include, for example, hydrocarbon halides having 1 to 10 carbon atoms, olefins having 2 to 10 carbon atoms, or styrenes having 8 to 10 carbon atoms, sulfuric acid, phosphoric acid, silicotungstic acid, hydrofluoric acid, etc. And a method of adding to naphthalene in the presence of an acid catalyst such as Friedel-Crafts catalyst which is a solid acidic substance such as mineral acid, acidic clay and activated clay, or a metal halide such as aluminum chloride and zinc chloride.

  Although it does not specifically limit as alkylbenzene concerning this invention, From the point which is excellent in compatibility with a refrigerant | coolant, it has 1-4 C1-C40 alkyl groups, and the total carbon number of an alkyl group is 1-40. Some are preferable, and those having 1 to 4 alkyl groups having 1 to 30 carbon atoms and having 3 to 30 carbon atoms in total are more preferable.

  Specific examples of the alkyl group having 1 to 40 carbon atoms that the alkylbenzene has include a methyl group, an ethyl group, an n-propyl group, an isopropyl group, a linear or branched butyl group, a linear or branched group. Pentyl group, linear or branched hexyl group, linear or branched heptyl group, linear or branched octyl group, linear or branched nonyl group, straight Linear or branched decyl group, linear or branched undecyl group, linear or branched dodecyl group, linear or branched tridecyl group, linear or branched Tetradecyl group, linear or branched pentadecyl group, linear or branched hexadecyl group, linear or branched heptadecyl group, linear or branched octadecyl group, linear -Like or branched nonadecyl group, linear or branched icosyl group, linear or branched Straight chain or branched docosyl group, linear or branched tricosyl group, linear or branched tetracosyl group, linear or branched pentacosyl group, straight chain Linear or branched hexacosyl group, linear or branched heptacosyl group, linear or branched octacosyl group, linear or branched nonacosyl group, linear or branched Triacontyl group, linear or branched hentriacontyl group, linear or branched dotriacontyl group, linear or branched tritriacontyl group, linear or branched tetra Triacontyl group, linear or branched pentatriacontyl group, linear or branched hexatriacontyl group, linear or branched heptatriacontyl group, linear Or branched octatriacontyl group, linear or branched Nona triacontyl group, such as straight or branched tetracontyl group (including all isomers).

  The alkyl group may be either linear or branched, but is preferably a linear alkyl group from the viewpoint of compatibility with the organic material used in the refrigerant circulation system. On the other hand, branched alkyl groups are preferable from the viewpoint of refrigerant compatibility, thermal stability, lubricity, etc., and branched alkyls derived from oligomers of olefins such as propylene, butene and isobutylene are particularly preferable from the viewpoint of availability. Groups are more preferred.

  In addition, when using alkylbenzene, the compound of a single structure may be used independently, and 2 or more types of the compounds from which a structure differs may be used in combination.

  Although the manufacturing method of the said alkylbenzene is arbitrary and is not limited at all, For example, it can manufacture by the synthesis method shown below.

  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, a linear or branched olefin having 6 to 40 carbon atoms obtained by polymerization of lower monoolefin (preferably propylene) such as ethylene, propylene, butene, isobutylene; wax, heavy oil, C6-C40 linear or branched olefins obtained by pyrolysis of petroleum fractions, polyethylene, polypropylene, etc .; n-paraffins are separated from petroleum fractions such as kerosene, light oil, etc. It is possible to use a linear olefin having 9 to 40 carbon atoms, a mixture of these, and the like obtained by converting into a carbon atom.

  In addition, when the aromatic compound and the alkylating agent are reacted, Friedel-Crafts type catalysts such as aluminum chloride and zinc chloride, sulfuric acid, phosphoric acid, silicotungstic acid, hydrofluoric acid, activated clay, etc. Conventionally known alkylation catalysts such as acidic catalysts can be used.

  Examples of the esters include aromatic esters, dibasic acid esters, polyol esters, complex esters, carbonate esters, and mixtures thereof.

  Examples of such aromatic esters include 1 to 6 valent, preferably 1 to 4 valent, more preferably 1 to 3 valent aromatic carboxylic acids, and aliphatic alcohols having 1 to 18 carbon atoms, preferably 1 to 12 carbon atoms. Examples include esters. Specific examples of the monovalent to hexavalent aromatic carboxylic acid include benzoic acid, phthalic acid, isophthalic acid, terephthalic acid, trimellitic acid, pyromellitic acid, and mixtures thereof. Further, the aliphatic alcohol having 1 to 18 carbon atoms may be linear or branched, and specifically, methanol, ethanol, linear or branched propanol, Linear or branched butanol, linear or branched pentanol, linear or branched hexanol, linear or branched heptanol, linear or branched octanol , Linear or branched nonanol, linear or branched decanol, linear or branched undecanol, linear or branched dodecanol, linear or branched tridecanol Linear or branched tetradecanol, linear or branched pentadecanol, linear or branched hexadecanol, linear or branched heptadecanol, straight Chain or branched octadecanol and these Mixtures thereof, and the like.

  Specific examples of the aromatic ester obtained by using the aromatic compound and the aliphatic alcohol include dibutyl phthalate, di (2-ethylhexyl) phthalate, dinonyl phthalate, didecyl phthalate, and didodecyl phthalate. , Ditridecyl phthalate, tributyl trimellitic acid, tri (2-ethylhexyl) trimellitic acid, trinonyl trimellitic acid, tridecyl trimellitic acid, tridodecyl trimellitic acid, and tritridecyl trimellitic acid. Of course, when a divalent or higher valent aromatic carboxylic acid is used, it may be a simple ester composed of one kind of aliphatic alcohol, or a complex ester composed of two or more kinds of aliphatic alcohol. May be.

  Examples of the dibasic acid ester include 5 to 10 carbon atoms such as glutaric acid, adipic acid, pimelic acid, suberic acid, azelaic acid, sebacic acid, 1,2-cyclohexanedicarboxylic acid, and 4-cyclohexene-1,2-dicarboxylic acid. A linear or cyclic aliphatic dibasic acid such as methanol, ethanol, propanol, butanol, pentanol, hexanol, heptanol, octanol, nonanol, decanol, undecanol, dodecanol, tridecanol, tetradecanol, pentadecanol, etc. A chain or branched ester with a monohydric alcohol having 1 to 15 carbon atoms and a mixture thereof are preferably used, and more specifically, ditridecyl glutarate, di2-ethylhexyl adipate, diisodecyl adipate, ditridecyl adipate, The 2 Ethylhexyl sebacate, diester of 1,2-cyclohexanedicarboxylic acid and monohydric alcohol having 4 to 9 carbon atoms, diester of 4-cyclohexene-1,2-dicarboxylic acid and monohydric alcohol having 4 to 9 carbon atoms, and these And the like.

  As the polyol ester, an ester of a polyol having 3 to 20 diols or hydroxyl groups and a fatty acid having 6 to 20 carbon atoms is preferably used. Specific examples of the diol include ethylene glycol, 1,3-propanediol, propylene glycol, 1,4-butanediol, 1,2-butanediol, 2-methyl-1,3-propanediol, , 5-pentanediol, neopentyl glycol, 1,6-hexanediol, 2-ethyl-2-methyl-1,3-propanediol, 1,7-heptanediol, 2-methyl-2-propyl-1,3 -Propanediol, 2,2-diethyl-1,3-propanediol, 1,8-octanediol, 1,9-nonanediol, 1,10-decanediol, 1,11-undecanediol, 1,12-dodecane Diol etc. are mentioned. Specific examples of the polyol include trimethylolethane, trimethylolpropane, trimethylolbutane, di- (trimethylolpropane), tri- (trimethylolpropane), pentaerythritol, di- (pentaerythritol), tri- ( Pentaerythritol), glycerin, polyglycerin (2-20 mer of glycerin), 1,3,5-pentanetriol, sorbitol, sorbitan, sorbitol glycerin condensate, polyvalent alcohols such as adonitol, arabitol, xylitol, mannitol, xylose Arabinose, ribose, rhamnose, glucose, fructose, galactose, mannose, sorbose, cellobiose, maltose, isomaltose, trehalose, sucrose, raffinose, gel Chianosu, sugars and their partial etherification such as melezitose, and methyl glucoside (glycoside) and the like. Among these, as the polyol, neopentyl glycol, trimethylol ethane, trimethylol propane, trimethylol butane, di- (trimethylol propane), tri- (trimethylol propane), pentaerythritol, di- (pentaerythritol), tri Hindered alcohols such as-(pentaerythritol) are preferred.

  In the fatty acid used in the polyol ester, the carbon number is not particularly limited, but those having 1 to 24 carbon atoms are usually used. Among the fatty acids having 1 to 24 carbon atoms, those having 3 or more carbon atoms are preferable from the viewpoint of lubricity, those having 4 or more carbon atoms are more preferable, those having 5 or more carbon atoms are further preferable, and those having 10 or more carbon atoms. Is particularly preferred. Moreover, from a compatibility point with a refrigerant | coolant, a C18 or less thing is preferable, a C12 or less thing is more preferable, and a C9 or less thing is further more preferable.

  The fatty acid may be either a linear fatty acid or a branched fatty acid, but a linear fatty acid is preferable from the viewpoint of lubricity, and a branched fatty acid is preferable from the viewpoint of hydrolysis stability. . Furthermore, the fatty acid may be either a saturated fatty acid or an unsaturated fatty acid.

  Specific examples of fatty acids include pentanoic acid, hexanoic acid, heptanoic acid, octanoic acid, nonanoic acid, decanoic acid, undecanoic acid, dodecanoic acid, tridecanoic acid, tetradecanoic acid, pentadecanoic acid, hexadecanoic acid, heptadecanoic acid, octadecanoic acid , Nonadecanoic acid, icosanoic acid, oleic acid, and the like. These fatty acids may be either linear fatty acids or branched fatty acids, and furthermore, fatty acids (neo) whose α carbon atom is a quaternary carbon atom. Acid). Among these, valeric acid (n-pentanoic acid), caproic acid (n-hexanoic acid), enanthic acid (n-heptanoic acid), caprylic acid (n-octanoic acid), pelargonic acid (n-nonanoic acid), caprin Acid (n-decanoic acid), oleic acid (cis-9-octadecenoic acid), isopentanoic acid (3-methylbutanoic acid), 2-methylhexanoic acid, 2-ethylpentanoic acid, 2-ethylhexanoic acid and 3,5,5 5-Trimethylhexanoic acid is preferably used.

  In addition, as long as it has two or more ester groups, the polyol ester according to the present invention may be a partial ester in which some of the hydroxyl groups of the polyol remain without being esterified. May be an esterified complete ester, or a mixture of a partial ester and a complete ester, but is preferably a complete ester.

  The complex ester is an ester of a fatty acid and a dibasic acid, and a monohydric alcohol and a polyol. As the fatty acid, dibasic acid, monohydric alcohol and polyol, in the description of the dibasic acid ester and the polyol ester, The exemplified fatty acids, dibasic acids, monohydric alcohols and polyols can be used.

Carbonic acid ester is represented by the following formula (1):
-O-CO-O- (1)
It is a compound which has the carbonate ester bond represented by these. The number of carbonate ester bonds represented by the above formula (1) may be one per molecule or two or more.

  As alcohol which comprises carbonate ester, the monohydric alcohol illustrated by the description of the said dibasic acid ester and polyol ester, a polyol, etc., and what added polyglycol to polyglycol and a polyol can be used. Moreover, you may use the compound obtained from a carbonic acid and a fatty acid and / or a dibasic acid.

  As a matter of course, when an ester is used, a compound having a single structure may be used alone, or two or more compounds having different structures may be used in combination.

  Among the above esters, dibasic acid ester, polyol ester, and carbonate ester are preferable because of excellent compatibility with the refrigerant.

  Furthermore, among dibasic acid esters, alicyclic dicarboxylic acid esters such as 1,2-cyclohexanedicarboxylic acid and 4-cyclohexene-1,2-dicarboxylic acid are compatible with refrigerants, and are stable in heat and hydrolysis. From the point of view, it is more preferable.

  Specific examples of the dibasic acid ester preferably used in the present invention include at least one monohydric alcohol selected from the group consisting of butanol, pentanol, hexanol, heptanol, octanol and nonanol, and 1,2-cyclohexanedicarboxylic acid. , Dibasic acid esters obtained from at least one dibasic acid selected from the group consisting of 4-cyclohexene-1,2-dicarboxylic acid, and mixtures thereof.

  In the dibasic acid ester according to the present invention, the low-temperature characteristics of the refrigerating machine oil composition and the compatibility with the refrigerant tend to be improved, so that there are two or more monohydric alcohols constituting the dibasic acid ester. It is preferable. The dibasic acid ester composed of two or more monohydric alcohols is a mixture of two or more esters of a dibasic acid and one alcohol, and a dibasic acid and two or more mixed alcohols. These esters are included.

  Among polyol esters, since they are more excellent in hydrolytic stability, neopentyl glycol, trimethylol ethane, trimethylol propane, trimethylol butane, di- (trimethylol propane), tri- (trimethylol propane), penta More preferred are esters of hindered alcohols such as erythritol, di- (pentaerythritol), tri- (pentaerythritol), more preferred are esters of neopentyl glycol, trimethylol ethane, trimethylol propane, trimethylol butane and pentaerythritol, The ester of pentaerythritol is most preferred because it is particularly excellent in compatibility with the refrigerant and hydrolytic stability.

  Specific examples of the polyol ester preferably used in the present invention include valeric acid, caproic acid, enanthic acid, caprylic acid, pelargonic acid, capric acid, oleic acid, isopentanoic acid, 2-methylhexanoic acid, 2-ethylpentanoic acid, From the group consisting of at least one fatty acid selected from the group consisting of 2-ethylhexanoic acid and 3,5,5-trimethylhexanoic acid, and neopentyl glycol, trimethylolethane, trimethylolpropane, trimethylolbutane and pentaerythritol. Examples include diesters, triesters, tetraesters and mixtures thereof obtained from at least one selected alcohol.

  In the polyol ester concerning this invention, since the low temperature characteristic of a refrigerating machine oil composition and the compatibility with a refrigerant | coolant tend to improve, it is preferable that the fatty acid which comprises a polyol ester is 2 or more types. The polyol ester composed of two or more fatty acids includes a mixture of two or more esters of polyol and one fatty acid, and an ester of a polyol and two or more mixed fatty acids. .

Among the carbonic acid esters, the following general formula (2):
^{_{(X 1 O) b -B- [}} O- (A 1 O) c -CO-O- (A 2 O) d -Y 1] a (2)
Wherein (2), ^{X 1} is a hydrogen atom, an alkyl group, a cycloalkyl group or the following general formula (3):
Y ^2- (OA ³ ) _e − (3)
(In formula (3), Y ² represents a hydrogen atom, an alkyl group or a cycloalkyl group, A ³ represents an alkylene group having 2 to 4 carbon atoms, and e represents an integer of 1 to 50)
A ¹ and A ² may be the same or different and each represents an alkylene group having 2 to 4 carbon atoms; Y ¹ represents a hydrogen atom, an alkyl group or a cycloalkyl group; Represents a residue of a compound having 3 to 20 hydroxyl groups, a represents 1 to 20, b represents an integer of 0 to 19 and a + b of 3 to 20, c represents an integer of 0 to 50, d Represents an integer of 1 to 50]
What has the structure represented by these is preferable.

In the above formula (2), X ¹ represents a hydrogen atom, an alkyl group, a cycloalkyl group or a group represented by the above formula (3). Although carbon number of an alkyl group here is not restrict | limited in particular, Usually, 1-24, Preferably it is 1-18, More preferably, it is 1-12. The alkyl group may be linear or branched.

  Specific examples of the alkyl group having 1 to 24 carbon atoms include methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, isobutyl group, sec-butyl group, tert-butyl group, linear chain Or a branched pentyl group, a linear or branched hexyl group, a linear or branched heptyl group, a linear or branched octyl group, a linear or branched nonyl group, a linear or branched decyl group, a linear or branched Branched undecyl group, linear or branched dodecyl group, linear or branched tridecyl group, linear or branched tetradecyl group, linear or branched pentadecyl group, linear or branched hexadecyl group, linear or branched heptadecyl Group, linear or branched octadecyl group, linear or branched nonadecyl group, linear or branched icosyl group, linear or branched heicosyl group, linear or branched docosyl group, linear or branched tricosyl group, Linear or branched tet Cosyl group, and the like.

  Specific examples of the cycloalkyl group include a cyclopentyl group, a cyclohexyl group, and a cycloheptyl group.

The alkylene group having 2 to 4 carbon atoms represented by A ³ in the formula (2) include an ethylene group, a propylene group, trimethylene group, butylene group, tetramethylene group, 1-methyltrimethylene group , 2-methyltrimethylene group, 1,1-dimethylethylene group, 1,2-dimethylethylene group and the like.

Y ² in the above formula (2) represents a hydrogen atom, an alkyl group or a cycloalkylalkyl group. Although carbon number of an alkyl group here is not restrict | limited in particular, Usually, 1-24, Preferably it is 1-18, More preferably, it is 1-12. The alkyl group may be linear or branched. Examples of the alkyl group having 1 to 24 carbon atoms include the alkyl groups exemplified in the description of X ¹ above.

  Specific examples of the cycloalkyl group include a cyclopentyl group, a cyclohexyl group, and a cycloheptyl group.

Among the groups represented by Y ² , a hydrogen atom or an alkyl group having 1 to 12 carbon atoms is preferable, and a hydrogen atom, a methyl group, an ethyl group, an n-propyl group, an iso-propyl group, an n-butyl group, an iso group. -Butyl group, sec-butyl group, tert-butyl group, n-pentyl group, iso-pentyl group, neo-pentyl group, n-hexyl group, iso-hexyl group, n-heptyl group, iso-heptyl group, n -Of the octyl group, iso-octyl group, n-nonyl group, iso-nonyl group, n-decyl group, iso-decyl group, n-undecyl group, iso-undecyl group, n-dodecyl group or iso-dodecyl group It is more preferable that it is either. E represents an integer of 1 to 50.

In addition, the group represented by X ¹ is preferably a hydrogen atom, an alkyl group having 1 to 12 carbon atoms, or a group represented by the general formula (3), and includes a hydrogen atom, a methyl group, an ethyl group, n-propyl group, iso-propyl group, n-butyl group, iso-butyl group, sec-butyl group, tert-butyl group, n-pentyl group, iso-pentyl group, neo-pentyl group, n-hexyl group, iso-hexyl group, n-heptyl group, iso-heptyl group, n-octyl group, iso-octyl group, n-nonyl group, iso-nonyl group, n-decyl group, iso-decyl group, n-undecyl group, It is more preferably any one of an iso-undecyl group, an n-dodecyl group, an iso-dodecyl group, or a group represented by the general formula (3).

  Specific examples of the compound having B as a residue and having 3 to 20 hydroxyl groups include the aforementioned polyols.

A ¹ and A ² may be the same or different and each represents an alkylene group having 2 to 4 carbon atoms. Specific examples of the alkylene group include ethylene, propylene, trimethylene, butylene, tetramethylene, 1-methyltrimethylene, 2-methyltrimethylene, 1,1-dimethylethylene, 1 , 2-dimethylethylene group and the like.

Y ¹ represents a hydrogen atom, an alkyl group or a cycloalkyl group. Although carbon number of an alkyl group here is not restrict | limited in particular, Usually, 1-24, Preferably it is 1-18, More preferably, it is 1-12. The alkyl group may be linear or branched. Specific examples of the alkyl group having 1 to 24 carbon atoms include the alkyl groups exemplified in the description of X ¹ .

  Specific examples of the cycloalkyl group include a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, and the like.

Among these, the group represented by Y ¹ is preferably a hydrogen atom or an alkyl group having 1 to 12 carbon atoms, and includes a hydrogen atom, a methyl group, an ethyl group, an n-propyl group, an iso-propyl group, n -Butyl group, iso-butyl group, sec-butyl group, tert-butyl group, n-pentyl group, iso-pentyl group, neo-pentyl group, n-hexyl group, iso-hexyl group, n-heptyl group, iso -Heptyl group, n-octyl group, iso-octyl group, n-nonyl group, iso-nonyl group, n-decyl group, iso-decyl group, n-undecyl group, iso-undecyl group, n-dodecyl group or iso -More preferably, it is one of dodecyl groups.

  In the above formulas (2) and (3), c, d and e represent the degree of polymerization of the polyoxyalkylene chain, but the polyoxyalkylene chains in the molecule may be the same or different. In addition, when the carbonic acid ester represented by the above formula (2) has a plurality of different polyoxyalkylene chains, there is no particular limitation on the polymerization mode of the oxyalkylene group, and block copolymerization is performed even if random copolymerization is performed. Also good.

  The method for producing the carbonate ester used in the present invention is arbitrary. For example, a polyalkylene glycol polyol ether is produced by adding an alkylene oxide to a polyol compound, and this and chloroformate are mixed with sodium hydroxide, hydroxide. It can be obtained by reacting at 0 to 30 ° C. in the presence of an alkali metal hydroxide such as potassium, an alkali metal alkoxide such as sodium methoxide or sodium ethoxide, or an alkali such as metal sodium. Or polyalkylene glycol polyol ether, carbonic acid diester, carbon dioxide such as phosgene, alkali metal hydroxide such as sodium hydroxide and potassium hydroxide, alkali metal alkoxide such as sodium methoxide and sodium ethoxide or metal sodium It can be obtained by reacting at 80 to 150 ° C. in the presence of an alkali such as. Thereafter, the free hydroxyl group is etherified as necessary.

  By-products and unreacted materials may be removed by purifying the product obtained from the above raw materials, but a small amount of by-products and unreacted materials impairs the excellent performance of the lubricating oil of the present invention. Unless it exists, there is no problem even if it exists.

In the present invention, when a carbonate ester is used, a compound having a single structure may be used alone, or two or more compounds having different structures may be used in combination. The molecular weight of the carbonate ester according to the present invention is not particularly limited, but the number average molecular weight is preferably 200 to 4000, more preferably 300 to 3000, from the viewpoint of further improving the hermeticity of the compressor. More preferred. Furthermore, the kinematic viscosity of such carbonic acid ester in the present invention, preferably at 100 ° C. is 2~150mm ² / s, more preferably 4~100mm ² / s.

Examples of the polyoxyalkylene glycol used in the lubricating oil of the present invention include the following general formula (4):
R ¹ - ^[(OR 2) _f -OR ^3] _g (4)
[In Formula (4), R ¹ represents a hydrogen atom, an alkyl group having 1 to 10 carbon atoms, an acyl group having 2 to 10 carbon atoms, or a residue of a compound having 2 to 8 hydroxyl groups, and R ² represents the number of carbon atoms. Represents an alkylene group having 2 to 4, R ³ represents a hydrogen atom, an alkyl group having 1 to 10 carbon atoms, or an acyl group having 2 to 10 carbon atoms, f represents an integer of 1 to 80, and g represents 1 to 8 Represents an integer]
The compound represented by these is mentioned.

In the general formula (4), the alkyl group represented by R ¹ and R ³ may be linear, branched or cyclic. Specific examples of the alkyl group include a methyl group, an ethyl group, an n-propyl group, an isopropyl group, a linear or branched butyl group, a linear or branched pentyl group, a linear or branched group. Hexyl group, linear or branched heptyl group, linear or branched octyl group, linear or branched nonyl group, linear or branched decyl group, cyclopentyl Group, cyclohexyl group and the like. If the alkyl group has more than 10 carbon atoms, the compatibility with the refrigerant is lowered, and phase separation tends to occur. The carbon number of a preferable alkyl group is 1-6.

Moreover, the alkyl group part of the acyl group represented by R ¹ and R ³ may be linear, branched, or cyclic. Specific examples of the alkyl group portion of the acyl group include those having 1 to 9 carbon atoms among the alkyl groups exemplified as the specific examples of the alkyl group. When the number of carbon atoms in the acyl group exceeds 10, compatibility with the refrigerant may be reduced, and phase separation may occur. A preferable acyl group has 2 to 6 carbon atoms.

When the groups represented by R ¹ and R ³ are both alkyl groups or are both acyl groups, the groups represented by R ¹ and R ³ may be the same or different. Further, when g is 2 or more, the groups represented by a plurality of R ¹ and R ³ in the same molecule may be the same or different.

When the group represented by R ¹ is a residue of a compound having 2 to 8 hydroxyl groups, this compound may be a chain or a cyclic one. Specific examples of the compound having two hydroxyl groups include ethylene glycol, 1,3-propanediol, propylene glycol, 1,4-butanediol, 1,2-butanediol, and 2-methyl-1,3-propanediol. 1,5-pentanediol, neopentyl glycol, 1,6-hexanediol, 2-ethyl-2-methyl-1,3-propanediol, 1,7-heptanediol, 2-methyl-2-propyl-1 , 3-propanediol, 2,2-diethyl-1,3-propanediol, 1,8-octanediol, 1,9-nonanediol, 1,10-decanediol, 1,11-undecanediol, 1,12 -Dodecanediol etc. are mentioned.

  Specific examples of the compound having 3 to 8 hydroxyl groups include trimethylolethane, trimethylolpropane, trimethylolbutane, di- (trimethylolpropane), tri- (trimethylolpropane), pentaerythritol, -(Pentaerythritol), tri- (pentaerythritol), glycerol, polyglycerol (glycerin 2-6 mer), 1,3,5-pentanetriol, sorbitol, sorbitan, sorbitol glycerol condensate, adonitol, arabitol, xylitol , Polyhydric alcohols such as mannitol, xylose, arabinose, ribose, rhamnose, glucose, fructose, galactose, mannose, sorbose, cellobiose, maltose, isomaltose, trehalose, skull Scan, raffinose, gentianose, saccharides such as rhamnose, and their partially etherified products, and include methyl glucoside (glycoside) and the like.

Among the polyoxyalkylene glycols represented by the general formula (4), at least one of R ¹ and R ³ is preferably an alkyl group (more preferably an alkyl group having 1 to 4 carbon atoms), particularly A methyl group is preferred from the viewpoint of refrigerant compatibility. Furthermore, from the viewpoint of thermal and chemical stability, it is preferable that both R ¹ and R ³ are alkyl groups (more preferably, alkyl groups having 1 to 4 carbon atoms), and particularly that both are methyl groups. Is preferred. From the viewpoint of ease of production and cost, it is preferable that either R ¹ or R ³ is an alkyl group (more preferably an alkyl group having 1 to 4 carbon atoms), and the other is a hydrogen atom. It is preferable that one is a methyl group and the other is a hydrogen atom.

R ² in the general formula (4) represents an alkylene group having 2 to 4 carbon atoms, and specific examples of such an alkylene group include an ethylene group, a propylene group, and a butylene group. Examples of the oxyalkylene group of the repeating unit represented by OR ² include an oxyethylene group, an oxypropylene group, and an oxybutylene group. The oxyalkylene groups in the same molecule may be the same, or two or more oxyalkylene groups may be included.

  Among the polyoxyalkylene glycols represented by the general formula (4), from the viewpoint of refrigerant compatibility and viscosity-temperature characteristics, a copolymer containing an oxyethylene group (EO) and an oxypropylene group (PO) is used. Preferably, in such a case, the ratio of the oxyethylene group to the total of the oxyethylene group and the oxypropylene group (EO / (PO + EO)) is 0.1 to 0.8 from the standpoint of baking load and viscosity-temperature characteristics. It is preferable that it exists in the range, and it is more preferable that it exists in the range of 0.3-0.6.

  In terms of hygroscopicity and thermal oxidation stability, the value of EO / (PO + EO) is preferably in the range of 0 to 0.5, more preferably in the range of 0 to 0.2, and 0 (that is, Most preferred is a propylene oxide homopolymer).

F in the said General formula (4) is an integer of 1-80, g is an integer of 1-8. For example, when R ⁷ is an alkyl group or an acyl group, g is 1. When R ⁷ is a residue of a compound having 2 to 8 hydroxyl groups, g is the number of hydroxyl groups that the compound has.

  In addition, the product of f and g (f × g) is not particularly limited, but in order to satisfy the required performance as the above-described lubricating oil for a refrigerator in a balanced manner, the average value of f × g is 6 to 80. It is preferable to do so.

Among the polyoxyalkylene glycols having the above configuration, the following general formula (5):
_{CH 3 O- (C 3 H 6} O) h -CH 3 (5)
(In the formula, h represents a number of 6 to 80)
And polyoxypropylene glycol dimethyl ether represented by the following general formula (6):
_{CH 3 O- (C 2 H 4} O) i - (C 3 H 6 O) j -CH 3 (6)
(In the formula, i and j are each 1 or more, and i and j represent a number of 6 to 80)
The polyoxyethylene polyoxypropylene glycol dimethyl ether represented by the formula is suitable from the viewpoint of economy and the above-mentioned effects, and the following general formula (7):
_{C 4 H 9 O- (C 3} H 6 O) k -H (7)
(In the formula, k represents a number of 6 to 80)
In addition, polyoxypropylene glycol monobutyl ether represented by the following general formula (8):
_{CH 3 O- (C 3 H 6} O) l -H (8)
(Wherein l represents a number from 6 to 80)
Polyoxypropylene glycol monomethyl ether represented by the following general formula (9):
_{CH 3 O- (C 2 H 4} O) m - (C 3 H 6 O) n -H (9)
(In the formula, m and n are each 1 or more, and the total of m and n represents 6 to 80)
Polyoxyethylene polyoxypropylene glycol monomethyl ether represented by the following general formula (10):
_{C 4 H 9 O- (C 2} H 4 O) m - (C 3 H 6 O) n -H (10)
(In the formula, m and n are each 1 or more, and the total of m and n represents 6 to 80)
Polyoxyethylene polyoxypropylene glycol monobutyl ether, the following general formula (11):
_{CH 3 COO- (C 3 H 6} O) l -COCH 3 (11)
(Wherein l represents a number from 6 to 80)
Is preferable in terms of economy and the like.

［式（１２）中、Ｒ^４〜Ｒ^７は同一でも異なっていてもよく、それぞれ水素原子、炭素数１〜１０の１価の炭化水素基又は下記一般式（１３）：

（式（１３）中、Ｒ^８及びＲ^９は同一でも異なっていてもよく、それぞれ水素原子、炭素数１〜１０の１価の炭化水素基又は炭素数２〜２０のアルコキシアルキル基を表し、Ｒ^１０は炭素数２〜５のアルキレン基、アルキル基を置換基として有する総炭素数２〜５の置換アルキレン基又はアルコキシアルキル基を置換基として有する総炭素数４〜１０の置換アルキレン基を表し、ｒは０〜２０の整数を表し、Ｒ^１３は炭素数１〜１０の１価の炭化水素基を表す）
で表される基を表し、Ｒ^８〜Ｒ^１１の少なくとも１つが一般式（１３）で表される基である］
で表される構成単位を少なくとも１個有するポリオキシアルキレングリコール誘導体を使用することができる。 In the present invention, the polyoxyalkylene glycol is represented by the general formula (12):

[In the formula (12), R ^{4 to} R ⁷ may be the same or different, and each represents a hydrogen atom, a monovalent hydrocarbon group having 1 to 10 carbon atoms, or the following general formula (13):

(In formula (13), R ⁸ and R ⁹ may be the same or different and each represents a hydrogen atom, a monovalent hydrocarbon group having 1 to 10 carbon atoms or an alkoxyalkyl group having 2 to 20 carbon atoms, R ¹⁰ represents an alkylene group having 2 to 5 carbon atoms, a substituted alkylene group having 2 to 5 carbon atoms having an alkyl group as a substituent, or a substituted alkylene group having 4 to 10 carbon atoms having an alkoxyalkyl group as a substituent. , R represents an integer of 0 to 20, and R ¹³ represents a monovalent hydrocarbon group having 1 to 10 carbon atoms)
Wherein at least one of R ^{8 to} R ¹¹ is a group represented by the general formula (13)]
A polyoxyalkylene glycol derivative having at least one structural unit represented by can be used.

In the above formula (12), R ^{4 to} R ⁷ each represent a hydrogen atom, a monovalent hydrocarbon group having 1 to 10 carbon atoms, or a group represented by the above general formula (13). Specific examples of the monovalent hydrocarbon group include a linear or branched alkyl group having 1 to 10 carbon atoms, a linear or branched alkenyl group having 2 to 10 carbon atoms, and carbon. Examples thereof include cycloalkyl groups or alkylcycloalkyl groups having 5 to 10 carbon atoms, aryl groups or alkylaryl groups having 6 to 10 carbon atoms, and arylalkyl groups having 7 to 10 carbon atoms. Among these monovalent hydrocarbon groups, a monovalent hydrocarbon group having 6 or less carbon atoms, particularly an alkyl group having 3 or less carbon atoms, specifically, a methyl group, an ethyl group, an n-propyl group, or an isopropyl group. preferable.

In the general formula (13), R ⁸ and R ⁹ each represent a hydrogen atom, a monovalent hydrocarbon group having 1 to 10 carbon atoms, or an alkoxyalkyl group having 2 to 20 carbon atoms. An alkyl group having a number of 3 or less or an alkoxyalkyl group having a carbon number of 6 or less is preferred. Specific examples of the alkyl group having 3 or less carbon atoms include a methyl group, an ethyl group, an n-propyl group, and an isopropyl group. Specific examples of the alkoxyalkyl group having 2 to 6 carbon atoms include methoxymethyl group, ethoxymethyl group, n-propoxymethyl group, isopropoxymethyl group, n-butoxymethyl group, isobutoxymethyl group, sec -Butoxymethyl group, tert-butoxymethyl group, pentoxymethyl group (including all isomers), methoxyethyl group (including all isomers), ethoxyethyl group (including all isomers), propoxyethyl Groups (including all isomers), butoxyethyl groups (including all isomers), methoxypropyl groups (including all isomers), ethoxypropyl groups (including all isomers), propoxypropyl groups ( All isomers included), methoxybutyl group (including all isomers), ethoxybutyl group (all isomers) Including), etc. methoxybutyl group (including all isomers).

In the general formula (13), R ¹⁰ is an alkylene group having 2 to 5 carbon atoms, a substituted alkylene group having 2 to 5 carbon atoms having an alkyl group as a substituent, or a total carbon number 4 having an alkoxyalkyl group as a substituent. Represents a substituted alkylene group having 10 to 10 carbon atoms, preferably an alkylene group having 2 to 4 carbon atoms and a substituted ethylene group having 6 or less carbon atoms in total. Specific examples of the alkylene group having 2 to 4 carbon atoms include an ethylene group, a propylene group, and a butylene group. Specific examples of the substituted ethylene group having 6 or less total carbon atoms include 1- (methoxymethyl) ethylene group, 2- (methoxymethyl) ethylene group, 1- (methoxyethyl) ethylene group, and 2- (methoxyethyl). ) Ethylene group, 1- (ethoxymethyl) ethylene group, 2- (ethoxymethyl) ethylene group, 1-methoxymethyl-2-methylethylene group, 1,1-bis (methoxymethyl) ethylene group, 2,2-bis (Methoxymethyl) ethylene group, 1,2-bis (methoxymethyl) ethylene group, 1-methyl-2-methoxymethylethylene group, 1-methoxymethyl-2-methylethylene group, 1-ethyl-2-methoxymethylethylene Group, 1-methoxymethyl-2-ethylethylene group, 1-methyl-2-ethoxymethylethylene group, 1-ethoxymethyl-2-methyl Ethylene, 1-methyl-2-methoxyethyl ethylene group, 1-methoxyethyl-2-methylethylene group, and the like.

In the general formula (13), R ¹¹ represents a monovalent hydrocarbon group having 1 to 10 carbon atoms. Specifically, the hydrocarbon group may be a straight chain having 1 to 10 carbon atoms or A branched alkyl group, a linear or branched alkenyl group having 2 to 10 carbon atoms, a cycloalkyl group or alkylcycloalkyl group having 5 to 10 carbon atoms, an aryl group or alkylaryl having 6 to 10 carbon atoms Group, an arylalkyl group having 7 to 10 carbon atoms, and the like. Among these, a monovalent hydrocarbon group having 6 or less carbon atoms is preferable, and an alkyl group having 3 or less carbon atoms, specifically, a methyl group, an ethyl group, an n-propyl group, or an isopropyl group is preferable.

In the general formula (12), at least one of R ^{4 to} R ⁷ is a group represented by the general formula (13). In particular, any one of R ^{4 and} R ⁶ is a group represented by the above general formula (13), and the other one of R ⁴ or R ⁶ and R ⁵ and R ⁷ are each a hydrogen atom or carbon. A monovalent hydrocarbon group having 1 to 10 is preferable.

［式（１４）中、Ｒ^１２〜Ｒ^１５は同一でも異なっていてもよく、それぞれ水素原子又は炭素数１〜３のアルキル基を示す］
で表される構成単位からなる共重合体の三種類に大別することができる。上記単独重合体の好適例は、一般式（１２）で表される構成単位Ａを１〜２００個有するとともに、末端基がそれぞれ水酸基、炭素数１〜１０のアシルオキシ基、炭素数１〜１０のアルコキシ基あるいはアリーロキシ基からなるものを挙げることができる。一方、共重合体の好適例は、一般式（１２）で表される二種類の構成単位Ａ、Ｂをそれぞれ１〜２００個有するか、あるいは一般式（１２）で表される構成単位Ａを１〜２００個と一般式（１２）で表される構成単位Ｃを１〜２００個有するとともに、末端基がそれぞれ水酸基、炭素数１〜１０のアシルオキシ基、炭素数１〜１０のアルコキシ基あるいはアリーロキシ基からなるものを挙げることができる。これらの共重合体は、構成単位Ａと構成単位Ｂ(あるいは構成単位Ｃ)との交互共重合、ランダム共重合、ブロック共重合体あるいは構成単位Ａの主鎖に構成単位Ｂがグラフト結合したグラフト共重合体のいずれの重合形式であってもよい。 The polyoxyalkylene glycol having a structural unit represented by the general formula (12), preferably used in the present invention, is a homopolymer consisting only of the structural unit represented by the general formula (12); And a copolymer composed of two or more structural units having different structures, and a structural unit represented by the general formula (12) and other structural units, for example, the following general formula (14):

[In the formula (14), R ^{12 to} R ¹⁵ may be the same or different and each represents a hydrogen atom or an alkyl group having 1 to 3 carbon atoms.]
Can be roughly divided into three types of copolymers consisting of structural units represented by: The preferred examples of the homopolymer have 1 to 200 structural units A represented by the general formula (12), and the terminal groups each have a hydroxyl group, an acyloxy group having 1 to 10 carbon atoms, and an alkyl group having 1 to 10 carbon atoms. The thing which consists of an alkoxy group or an aryloxy group can be mentioned. On the other hand, suitable examples of the copolymer have 1 to 200 of the two types of structural units A and B represented by the general formula (12), or the structural unit A represented by the general formula (12). 1 to 200 and 1 to 200 structural units C represented by the general formula (12), and each terminal group is a hydroxyl group, an acyloxy group having 1 to 10 carbon atoms, an alkoxy group having 1 to 10 carbon atoms, or aryloxy The thing which consists of groups can be mentioned. These copolymers include alternating copolymerization of the structural unit A and the structural unit B (or the structural unit C), a random copolymer, a block copolymer, or a graft in which the structural unit B is graft-bonded to the main chain of the structural unit A. Any polymerization form of the copolymer may be used.

［式（１５）中、Ｒ^１６〜Ｒ^１８は同一でも異なっていてもよく、それぞれ水素原子又は炭素数１〜８の炭化水素基を表し、Ｒ^１９は炭素数１〜１０の２価の炭化水素基又は炭素数２〜２０の２価のエーテル結合酸素含有炭化水素基を表し、Ｒ^２０は炭素数１〜２０の炭化水素基を表し、ｓはその平均値が０〜１０の数を表し、Ｒ^１６〜Ｒ^２０は構成単位毎に同一であってもそれぞれ異なっていてもよく、また一般式（１５）で表される構成単位が複数のＲ^１９Ｏを有するとき、複数のＲ^１９Ｏは同一でも異なっていてもよい］
で表される構成単位を有するポリビニルエーテル系化合物が挙げられる。 Examples of the polyvinyl ether used in the present invention include the following general formula (15):

[In the formula (15), R ^{16 to} R ¹⁸ may be the same or different and each represents a hydrogen atom or a hydrocarbon group having 1 to 8 carbon atoms, and R ¹⁹ is a divalent carbon atom having 1 to 10 carbon atoms. Represents a hydrogen group or a divalent ether-bonded oxygen-containing hydrocarbon group having 2 to ²⁰ carbon atoms, R ²⁰ represents a hydrocarbon group having 1 to ²⁰ carbon atoms, and s represents a number having an average value of 0 to 10. , R ^{16 to} R ²⁰ may be the same or different for each structural unit, and when the structural unit represented by the general formula (15) has a plurality of R ¹⁹ O, a plurality of R ¹⁹ Os. May be the same or different.]
The polyvinyl ether type compound which has a structural unit represented by these is mentioned.

［式（１６）中、Ｒ^２１〜Ｒ^２４は同一でも異なっていてもよく、それぞれ水素原子又は炭素数１〜２０の炭化水素基を表し、Ｒ^２１〜Ｒ^２４は構成単位毎に同一でも異なっていてもよい］
で表される構成単位とを有するブロック共重合体又はランダム共重合体からなるポリビニルエーテル系化合物も使用することができる。 Moreover, the structural unit represented by the above general formula (15) and the following general formula (16):

[In Formula (16), R ^{21 to} R ²⁴ may be the same or different and each represents a hydrogen atom or a hydrocarbon group having 1 to 20 carbon atoms, and R ^{21 to} R ²⁴ are the same or different for each constituent unit. It may be]
A polyvinyl ether compound comprising a block copolymer or a random copolymer having a structural unit represented by

R ^{16 to} R ¹⁸ in the general formula (15) each represent a hydrogen atom or a hydrocarbon group having 1 to 8 carbon atoms (preferably 1 to 4 hydrocarbon group), and they may be the same or different from each other. Good. Specific examples of the hydrocarbon group include methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, isobutyl group, sec-butyl group, tert-butyl group, various pentyl groups, and various hexyl groups. Group, various heptyl groups, various octyl groups and other alkyl groups; cyclopentyl group, cyclohexyl group, various methylcyclohexyl groups, various ethylcyclohexyl groups, various dimethylcyclohexyl groups and other cycloalkyl groups, phenyl groups, various methylphenyl groups, various ethyl groups An aryl group such as a phenyl group and various dimethylphenyl groups; an arylalkyl group such as a benzyl group, various phenylethyl groups, and various methylbenzyl groups, and the like can be mentioned, and R ^{22 to} R ²⁴ are preferably an elementary atom.

On the other hand, R ¹⁹ in the general formula (15) is a divalent hydrocarbon group having 1 to 10 carbon atoms (preferably 2 to 10) or a divalent ether bond oxygen-containing hydrocarbon group having 2 to 20 carbon atoms. Represents. Specific examples of the divalent hydrocarbon group having 1 to 10 carbon atoms include methylene group, ethylene group, phenylethylene group, 1,2-propylene group, 2-phenyl-1,2-propylene group, 1, Divalent aliphatic chain hydrocarbon groups such as 3-propylene group, various butylene groups, various pentylene groups, various hexylene groups, various heptylene groups, various octylene groups, various nonylene groups, and various decylene groups; cyclohexane, methylcyclohexane, Cycloaliphatic hydrocarbon groups having two bonding sites on cycloaliphatic hydrocarbons such as ethylcyclohexane, dimethylcyclohexane, propylcyclohexane; various phenylene groups, various methylphenylene groups, various ethylphenylene groups, various dimethylphenylene groups, various Divalent aromatic hydrocarbon groups such as naphthylene groups; toluene, xylene, ethylbenzene, etc. An alkyl aromatic hydrocarbon group having a monovalent bonding site on each of the alkyl group part and the aromatic part of the alkyl aromatic hydrocarbon; an alkyl having a binding site on the alkyl group part of a polyalkyl aromatic hydrocarbon such as xylene or diethylbenzene An aromatic hydrocarbon group, and the like. Among these, an aliphatic chain hydrocarbon group having 2 to 4 carbon atoms is particularly preferable.

Specific examples of the divalent ether bond oxygen-containing hydrocarbon group having 2 to 20 carbon atoms include methoxymethylene group, methoxyethylene group, methoxymethylethylene group, 1,1-bismethoxymethylethylene group, 1,2 Preferred examples include -bismethoxymethylethylene group, ethoxymethylethylene group, (2-methoxyethoxy) methylethylene group, (1-methyl-2-methoxy) methylethylene group, and the like. Incidentally, s in the general formula (15) represents a repeating number of ^{R 19} O, the average value thereof is 0 to 10, preferably a number in the range of 0-5. When the R ^{19 O} is more, the same configuration units, a plurality of R ^{19 O} may be the same or different.

Furthermore, R ²⁰ in the general formula (15) represents a hydrocarbon group having 1 to ²⁰ carbon atoms, preferably 1 to 10 carbon atoms. Specific examples of the hydrocarbon group include a methyl group, an ethyl group, and n. -Propyl group, isopropyl group, n-butyl group, isobutyl group, sec-butyl group, tert-butyl group, various pentyl groups, various hexyl groups, various heptyl groups, various octyl groups, various nonyl groups, various decyl groups, etc. Alkyl group: Cyclopentyl group, cyclohexyl group, various methylcyclohexyl groups, various ethylcyclohexyl groups, various propylcyclohexyl groups, various dimethylcyclohexyl groups and other cycloalkyl groups; phenyl group, various methylphenyl groups, various ethylphenyl groups, various dimethylphenyls Groups, various propylphenyl groups, various trimethylphenyl groups, various types Examples include aryl groups such as butylphenyl group and various naphthyl groups; arylalkyl groups such as benzyl group, various phenylethyl groups, various methylbenzyl groups, various phenylpropyl groups, and various phenylbutyl groups. R ^{22 to} R ²⁶ may be the same or different for each structural unit.

  When the polyvinyl ether according to the present invention is a homopolymer consisting only of the structural unit represented by the general formula (15), the carbon / oxygen molar ratio is preferably in the range of 4.2 to 7.0. . If the molar ratio is less than 4.2, the hygroscopicity becomes excessively high, and if it exceeds 7.0, the compatibility with the refrigerant tends to be reduced.

In the general formula (16), R ^{21 to} R ²⁴ may be the same or different and each represents a hydrogen atom or a hydrocarbon group having 1 to 20 carbon atoms. Examples of the hydrocarbon group having 1 to 20 carbon atoms, and hydrocarbon groups exemplified in the description of R ²⁰ in the general formula (15). R ^{21 to} R ²⁴ may be the same or different for each structural unit.

  When the polyvinyl ether according to the present invention is a block copolymer or a random copolymer having a structural unit represented by the general formula (15) and a structural unit represented by the general formula (16), the carbon / oxygen The molar ratio is preferably in the range of 4.2 to 7.0. If the molar ratio is less than 4.2, the hygroscopicity becomes excessively high, and if it exceeds 7.0, the compatibility with the refrigerant tends to be reduced.

  Furthermore, in this invention, the homopolymer which consists only of the structural unit represented by the said General formula (15), the structural unit represented by the said General formula (15), and the structure represented by the said General formula (16) Mixtures of block copolymers or random copolymers composed of units can also be used. These homopolymers and copolymers can be produced by polymerization of corresponding vinyl ether monomers and copolymerization of corresponding hydrocarbon monomers having olefinic double bonds and corresponding vinyl ether monomers.

［式（１７）中、Ｒ^２５〜Ｒ^２７は同一でも異なっていてもよく、それぞれ水素原子又は炭素数１〜８の炭化水素基を表し、Ｒ^２８は炭素数１〜１０の２価の炭化水素基又は炭素数２〜２０の２価のエーテル結合酸素含有炭化水素基を表し、Ｒ^２９は炭素数１〜２０の炭化水素基を表し、ｔはその平均値が０〜１０の数を表し、上記一般式（１７）で表される末端構造が複数のＲ^２８Ｏを有するとき、複数のＲ^２８Ｏはそれぞれ同一でも異なっていてもよい］

［式（１８）中、Ｒ^３０〜Ｒ^３１は同一でも異なっていてもよく、それぞれ水素原子又は炭素数１〜２０の炭化水素基を表す］
で表されるものであり、且つ他方が下記一般式（１９）又は（２０）：

［式（１９）中、Ｒ^３４〜Ｒ^３６は同一でも異なっていてもよく、それぞれ水素原子又は炭素数１〜８の炭化水素基を表し、Ｒ^３７は炭素数１〜１０の２価の炭化水素基又は炭素数２〜２０の２価のエーテル結合酸素含有炭化水素基を表し、Ｒ^３８は炭素数１〜２０の炭化水素基を表し、ｔはその平均値が０〜１０の数を表し、上記一般式（１９）で表される末端構造が複数のＲ^３７Ｏを有するとき、複数のＲ^３７Ｏはそれぞれ同一でも異なっていてもよい］

［式（２０）中、Ｒ^３９〜Ｒ^４２は同一でも異なっていてもよく、それぞれ水素原子又は炭素数１〜２０の炭化水素基を表す］
で表される構造を有するもの；及び
その末端の一方が、上記一般式（１７）又は（１８）で表され、且つ他方が下記一般式（２１）：

［式（２１）中、Ｒ^４３〜Ｒ^４５は同一でも異なっていてもよく、それぞれ水素原子又は炭素数１〜８の炭化水素基を表す］
で表される構造を有するものが好ましい。このようなポリビニルエーテルの中でも、次に挙げるものが特に好適である。 As the polyvinyl ether used in the present invention, one of the terminal structures has the following general formula (17) or (18):

[In Formula (17), R ^{25 to} R ²⁷ may be the same or different and each represents a hydrogen atom or a hydrocarbon group having 1 to 8 carbon atoms; R ²⁸ is a divalent carbon atom having 1 to 10 carbon atoms; Represents a hydrogen group or a divalent ether-bonded oxygen-containing hydrocarbon group having 2 to 20 carbon atoms, R ²⁹ represents a hydrocarbon group having 1 to 20 carbon atoms, and t represents a number having an average value of 0 to 10. When the terminal structure represented by the general formula (17) has a plurality of R ²⁸ Os, the plurality of R ²⁸ Os may be the same or different.

[In the formula (18), R ^{30 to} R ³¹ may be the same or different and each represents a hydrogen atom or a hydrocarbon group having 1 to 20 carbon atoms]
And the other is represented by the following general formula (19) or (20):

[In the formula (19), R ^{34 to} R ³⁶ may be the same or different, and each represents a hydrogen atom or a hydrocarbon group having 1 to 8 carbon atoms, and R ³⁷ is a divalent carbon atom having 1 to 10 carbon atoms. Represents a hydrogen group or a divalent ether-bonded oxygen-containing hydrocarbon group having 2 to 20 carbon atoms, R ³⁸ represents a hydrocarbon group having 1 to 20 carbon atoms, and t represents a number having an average value of 0 to 10. When the terminal structure represented by the general formula (19) has a plurality of R ³⁷ O, the plurality of R ³⁷ O may be the same or different from each other]

[In Formula (20), R ^{39 to} R ⁴² may be the same or different and each represents a hydrogen atom or a hydrocarbon group having 1 to 20 carbon atoms]
One of its ends is represented by the above general formula (17) or (18), and the other is represented by the following general formula (21):

[In formula (21), R ^{43 to} R ⁴⁵ may be the same or different and each represents a hydrogen atom or a hydrocarbon group having 1 to 8 carbon atoms]
What has the structure represented by these is preferable. Among such polyvinyl ethers, the following are particularly suitable.

(1) One of the terminals has a structure represented by General Formula (17) or (18) and the other is represented by General Formula (19) or (20), and R ¹⁶ in General Formula (15) -R ¹⁸ are all hydrogen atoms, s is a number from 0 to 4, R ¹⁹ is a divalent hydrocarbon group having 2 to 4 carbon atoms, and R ²⁰ is a carbon atom having 1 to ²⁰ carbon atoms. Being a hydrogen group;
(2) It has only the structural unit represented by the general formula (15), and one end of the structural unit is represented by the general formula (17) and the other has a structure represented by the general formula (18). R ^{16 to} R ¹⁸ in the general formula (15) are all hydrogen atoms, s is a number from 0 to 4, and R ¹⁹ is a divalent hydrocarbon group having 2 to 4 carbon atoms. And R ²⁰ is a hydrocarbon group having 1 to ²⁰ carbon atoms;
(3) One of the terminals has a structure represented by the general formula (17) or (18) and the other is represented by the general formula (19), and R ^{16 to} R ¹⁸ in the general formula (15) are All are hydrogen atoms, s is a number from 0 to 4, R ¹⁹ is a divalent hydrocarbon group having 2 to 4 carbon atoms, and R ²⁰ is a hydrocarbon group having 1 to ²⁰ carbon atoms. thing;
(4) It has only the structural unit represented by the general formula (15), and one end thereof is represented by the general formula (17) and the other has a structure represented by the general formula (20). R ^{16 to} R ¹⁸ in the general formula (15) are all hydrogen atoms, s is a number from 0 to 4, and R ¹⁹ is a divalent hydrocarbon group having 2 to 4 carbon atoms. R ²⁰ is a hydrocarbon group having 1 to ²⁰ carbon atoms.

［式（２２）中、Ｒ^４６〜Ｒ^４８は同一でも異なっていてもよく、それぞれ水素原子又は炭素数１〜８の炭化水素基を表し、Ｒ^４９及びＲ^５１は同一でも異なっていてもよく、それぞれ炭素数２〜１０の２価の炭化水素基を表し、Ｒ^５０及びＲ^５２は同一でも異なっていてもよく、それぞれ炭素数１〜１０の炭化水素基を表し、ｕ及びｖは同一でも異なっていてもよく、それぞれその平均値が０〜１０の数を表し、上記一般式（２２）で表される末端構造が複数のＲ^４９Ｏ又はＲ^５１Ｏを有するとき、複数のＲ^４９Ｏ又はＲ^５１Ｏは同一であっても異なっていてもよい］
で表される構造を有するポリビニルエーテル系化合物も使用することができる。 Moreover, in this invention, it has a structural unit represented by the said General formula (15), One of the terminal is represented by General formula (17), and the other is following General formula (22):

[In the formula (22), R ^{46 to} R ⁴⁸ may be the same or different, each represents a hydrogen atom or a hydrocarbon group having 1 to 8 carbon atoms, and R ⁴⁹ and R ⁵¹ may be the same or different. Each represents a divalent hydrocarbon group having 2 to 10 carbon atoms, R ⁵⁰ and R ⁵² may be the same or different, each represents a hydrocarbon group having 1 to 10 carbon atoms, and u and v may be the same. When the terminal structure represented by the general formula (22) has a plurality of R ⁴⁹ O or R ⁵¹ O, the average value thereof may be different, and each of the average values represents a number of R ⁴⁹ O. Or R ⁵¹ O may be the same or different.]
A polyvinyl ether compound having a structure represented by the formula can also be used.

［式（２３）中、Ｒ^５３は炭素数１〜８の炭化水素基を示す］

［式（２４）中、Ｒ^５４は炭素数１〜８の炭化水素基を示す］
で表される構成単位からなり、かつ重量平均分子量が３００〜５,０００であって、末端の一方が下記一般式（２５）又は（２６）：

［式（２５）中、Ｒ^５５は炭素数１〜３のアルキル基を表し、Ｒ^５６は炭素数１〜８の炭化水素基を示す］

［式（２６）中、Ｒ^５７は炭素数１〜８の炭化水素基を示す］
で表される構造を有するアルキルビニルエーテルの単独重合物又は共重合物からなるポリビニルエーテル系化合物も使用することができる。 Furthermore, in the present invention, the following general formula (23) or (24):

[In formula (23), R ⁵³ represents a hydrocarbon group having 1 to 8 carbon atoms]

[In the formula (24), R ⁵⁴ represents a hydrocarbon group having 1 to 8 carbon atoms]
And the weight average molecular weight is 300 to 5,000, and one of the terminals is represented by the following general formula (25) or (26):

[In the formula (25), R ⁵⁵ represents an alkyl group having 1 to 3 carbon atoms, and R ⁵⁶ represents a hydrocarbon group having 1 to 8 carbon atoms]

[In formula (26), R ⁵⁷ represents a hydrocarbon group having 1 to 8 carbon atoms]
A polyvinyl ether compound comprising a homopolymer or copolymer of an alkyl vinyl ether having a structure represented by

  In the present invention, only one kind selected from the group consisting of the mineral oil and the synthetic oil described above may be used alone, or two or more kinds may be used in combination. When the refrigerating machine oil composition of the present invention is used in an open type compressor such as a car air conditioner using an HFC refrigerant, among the above-described mineral oil and synthetic oil, polyoxyalkylene glycol, ester, and polyvinyl ether are preferable. . Moreover, when using the refrigerator oil composition of this invention for closed compressors, such as a refrigerator and an air conditioning apparatus, alkylbenzene, ester, and polyvinyl ether are preferable.

  Further, the refrigerating machine oil composition of the present invention comprises at least one nitrogen-containing oily agent selected from (A1) amine, (A2) amine carboxylate and (A3) amide (hereinafter these are collectively referred to as “( A) a nitrogen-containing oil-based agent ”).

  Among the (A) nitrogen-containing oily agents, examples of the (A1) 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), Propylamine (including all isomers), monobutylamine (including all isomers), dibutylamine (including all isomers), tributylamine (including all isomers), monopentylamine (all including all isomers) Including 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) ), Monooctylamine (including all isomers), dioctylamine (including all isomers), monononylamine (including all isomers), monodecylamine (including all isomers), monoundecyl (Including all isomers), monododecylamine (including all isomers), monotridecylamine (including all isomers), monotetradecylamine (including all isomers), monopentadecyl Amine (including all isomers), monohexadecylamine (including all isomers), monoheptadecylamine (including all isomers), monooctadecylamine (including all isomers), mononona Decylamine (including all isomers), monoicosylamine (including all isomers), monohenicosylamine (including all isomers), monodocosyl Min (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 (all isomers) ), Dimethyl (dodecyl) amine (including all isomers), dimethyl (tridecyl) amine (including all isomers), dimethyl (tetradecyl) ) Amine (including all isomers), dimethyl (pentadecyl) amine (including all isomers), dimethyl (hexadecyl) amine (including all isomers), dimethyl (heptadecyl) amine (all isomers) ), Dimethyl (octadecyl) amine (including all isomers), dimethyl (nonadecyl) amine (including all isomers), dimethyl (icosyl) amine (including all isomers), dimethyl (henicosyl) Alkylamines such as amines (including all isomers), dimethyl (tricosyl) amine (including all isomers); monovinylamine, divinylamine, trivinylamine, monopropenylamine (including all isomers), Dipropenylamine (including all isomers), tripropenylamine (including all isomers), monobutene Ruamine (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 (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 (all ), Monoheptadecenylamine (including all isomers), monooctadecenylamine (including all isomers), monononadecenylamine (including all isomers), monoico Cenylamine (including all isomers), Monohenicocenylamine (including all isomers), Monodocosenylamine (including all isomers), Monotricocenylamine (including all isomers) Alkenylamines 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 (all Isomers), dimethyl (nonenyl) amine (including 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 (pentadecenyl) amine (all isomers) ), Dimethyl (hexadecenyl) amine (including all isomers), dimethyl (heptadecenyl) amino (Including all isomers), dimethyl (octadecenyl) amine (including all isomers), dimethyl (nonadecenyl) amine (including all isomers), dimethyl (icosenyl) amine (including all isomers) , Monoamines having an alkyl group and an alkenyl group such as dimethyl (henicosenyl) amine (including all isomers), dimethyl (tricosenyl) amine (including all isomers); monobenzylamine, (1-phenyltyl) amine, Aromatic substituted alkylamines such as (2-phenylethyl) amine (also known as monophenethylamine), dibenzylamine, bis (1-phenethyl) amine, bis (2-phenylethylene) amine (also known as diphenethylamine); monocyclopentyl Amine, dicyclopentylamine, tricyclopentyla Cycloalkylamines having 5 to 16 carbon atoms such as dimethyl, cyclocyclohexylamine, dicyclohexylamine, monocycloheptylamine, dicycloheptylamine; dimethyl (cyclopentyl) amine, dimethyl (cyclohexyl) amine, dimethyl (cycloheptyl) amine, etc. Monoamines having alkyl and cycloalkyl groups; (methylcyclopentyl) amine (including all substituted isomers), bis (methylcyclopentyl) amine (including all substituted isomers), (dimethylcyclopentyl) amine (all substituted isomers) Isomers), bis (dimethylcyclopentyl) amine (including all substituted isomers), (ethylcyclopentyl) amine (including all substituted isomers), bis (ethylcyclopentyl) amine (including all substituted isomers) Including), (me Tilethylcyclopentyl) amine (including all substituted isomers), bis (methylethylcyclopentyl) amine (including all substituted isomers), (diethylcyclopentyl) amine (including all substituted isomers), (methylcyclohexyl) ) Amine (including all substituted isomers), bis (methylcyclohexyl) amine (including 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 (all substituted isomers) Isomers), (diethylcyclohexyl) amine (all substituted isomers) Including), (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 (including all substituted isomers), (diethylcycloheptyl) amine (including all substituted isomers), etc. An alkylcycloalkylamine of the formula; The monoamine also includes monoamines derived from fats and oils such as beef tallow amine.

  Among the monoamines, alkylamines and alkenylamines are preferable from the viewpoint of friction characteristics, and monoamines represented by the following general formula (A-1) are more preferable.

In the general formula (A-1), R ⁵⁸ represents an alkyl group having 8 to 30 carbon atoms or an alkenyl group having 8 to 30 carbon atoms. R ⁵⁸ is preferably an alkyl group having 10 to 24 carbon atoms or an alkenyl group having 10 to 24 carbon atoms, and more preferably an alkyl group having 12 to 18 carbon atoms or an alkenyl group having 12 to 18 carbon atoms. .

In the general formula (A-1), R ⁵⁹ and R ⁶⁰ may be the same or different and each represents a hydrogen atom, an alkyl group having 1 to 18 carbon atoms, or an alkenyl group having 1 to 18 carbon atoms. R ⁵⁹ and R ⁶⁰ are preferably a hydrogen atom or an alkyl group having 1 to 6 carbon atoms, more preferably a hydrogen atom or 1 to 4 carbon atoms, and still more preferably a hydrogen atom or a methyl group. , R ⁵⁹ and R ⁶⁰ are particularly preferably methyl groups.

  Specific examples of the polyamine include, for example, ethylenediamine, diethylenetriamine, triethylenetetramine, tetraethylenepentamine, pentaethylenehexamine, propylenediamine, dipropylenetriamine, tripropylenetetramine, tetrapropylenepentamine, pentapropylenehexamine, butylene. Alkylene polyamines such as diamine, dibutylenetriamine, tributylenetetramine, tetrabutylenepentamine, pentabylenehexamine; N-methylethylenediamine, N-ethylethylenediamine, N-propylethylenediamine (including all isomers), N-butylethylenediamine (Including all isomers), N-pentylethylenediamine (including all isomers), N-hexylethylenediamine (including all isomers) All isomers), N-heptylethylenediamine (including all isomers), N-octylethylenediamine (including all isomers), N-nonylethylenediamine (including all isomers), N-decyl Ethylenediamine (including all isomers), N-undecyl (including all isomers), N-dodecylethylenediamine (including all isomers), N-tridecylethylenediamine (including all isomers), N -Tetradecylethylenediamine (including all isomers), N-pentadecylethylenediamine (including all isomers), N-hexadecylethylenediamine (including all isomers), N-heptadecylethylenediamine (all isomers) N-octadecylethylenediamine (including all isomers), N-nonadecyl ester Range amine (including all isomers), N-icosylethylenediamine (including all isomers), N-henicosylethylenediamine (including all isomers), N-docosylethylenediamine (all isomers) N-tricosylethylenediamine (including all isomers) and the like; N-vinylethylenediamine, N-propenylethylenediamine (including all isomers), N-butenylethylenediamine (all Isomers), N-pentenylethylenediamine (including all isomers), N-hexenylethylenediamine (including all isomers), N-heptenylethylenediamine (including all isomers), N-octenyl Ethylenediamine (including all isomers), N-nonenylethylenediamine (all ), N-decenylethylenediamine (including all isomers), N-undecenyl (including all isomers), N-dodecenylethylenediamine (including all isomers), N-tridecenylethylenediamine (including all isomers), N-tetradecenylethylenediamine (including all isomers), N-pentadecenylethylenediamine (including all isomers), N-hexa Decenylethylenediamine (including all isomers), N-heptadecenylethylenediamine (including all isomers), N-octadecenylethylenediamine (including all isomers), N-nonadece Nylethylenediamine (including all isomers), N-icosenylethylenediamine (including all isomers), N-henicocenylethylenediamine (all isomers) N-alkenylethylenediamine such as 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-alkenylpentaethylenehexamine, N-alkylpropylenediamine, N-alkenyl propylene diamine, N-alkyl dipropylene triamine, N-alkenyl dipropylene triamine, N-alkyl tripropylene tetramine, N-alkenyl tripropylene tetrato N-alkyltetrapropylenepentamine, N-alkenyltetrapropylenepentamine, N-alkylpentapropylenehexamine, N-alkenylpentapropylenehexamine, N-alkylbutylenediamine, N-alkenylbutylenediamine, N-alkyldibutylenetriamine N-alkenyldibutylenetriamine, N-alkyltributylenetetramine, N-alkenyltributylenetetramine, N-alkyltetrabutylenepentamine, N-alkenyltetrabutylenepentamine, N-alkylpentabutylenehexamine, N-alkenylpentabutylene N-alkyl or N-alkenyl alkylene polyamines such as hexamine; The polyamine also includes polyamines derived from fats and oils such as beef tallow polyamines. Specific examples of the alkanolamine include monomethanolamine, dimethanolamine, trimethanolamine, monoethanolamine, diethanolamine, triethanolamine, mono (n-propanol) amine, and di (n-propanol) amine. , Tri (n-propanol) amine, monoisopropanolamine, diisopropanolamine, triisopropanolamine, monobutanolamine (including all isomers), dibutanolamine (including all isomers), tributanolamine (all ), Monopentanolamine (including all isomers), dipentanolamine (including all isomers), tripentanolamine (including all isomers), monohexanolamine (including all isomers) Including all isomers) Dihexanolamine (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 included), diethyl monoethanolamine, diethyl monopropanolamine (including all isomers), diethyl monobutanol Amine (including all isomers), Diethyl monopentanolamine (including all isomers), Dipropyl monoethanolamine (including all isomers), Dipropyl monopropanolamine (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), monoethyldipe Tertanolamine (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 And monobutyldipentanolamine (including all isomers) and the like.

  As an alkanolamine used by this invention, the alkanolamine represented by the following general formula (A-2) is preferable.

In the general formula (A-2), R ⁶¹ represents an alkyl group having 8 to 30 carbon atoms or an alkenyl group having 8 to 30 carbon atoms. R ⁶¹ is preferably an alkyl group having 10 to 24 carbon atoms or an alkenyl group having 10 to 24 carbon atoms, and more preferably an alkyl group having 12 to 18 carbon atoms or an alkenyl group having 12 to 18 carbon atoms. .

Further, in the above general formula ^{(A-2), R 62} represents an alkanol group. The alkanol group represented by R ^62, preferred alkanol group having 1 to 18 carbon atoms, more preferably an alkanol group having 1 to 6 carbon atoms, particularly preferably an alkanol group having 1 or 2 carbon atoms.

Further, in the above general formula ^{(A-2), R 63} represents a hydrogen atom, an alkanol group or an alkyl group having 1 to 18 carbon atoms. R ⁶³ is preferably an alkanol group or an alkyl group, and more preferably an alkanol group. When R ⁶³ is an alkanol group, the alkanol group is preferably an alkanol group having 1 to 18 carbon atoms, more preferably an alkanol group having 1 to 6 carbon atoms, and particularly preferably an alkanol group having 1 or 2 carbon atoms. When R ⁶³ is an alkyl group, the alkyl group is more preferably an alkyl group having 1 to 6 carbon atoms, further preferably an alkyl group having 1 to 4 carbon atoms, and an alkyl group having 1 or 2 carbon atoms. Particularly preferred.

  Among the above amines, monoamines and alkanolamines are preferable, and alkanolamines are more preferable from the viewpoint of friction characteristics.

  In addition, examples of the carboxylate of (A2) amine include the above-mentioned monoamine, polyamine, and alkanolamine carboxylates. (A2) The amine constituting the amine carboxylic acid is preferably a monoamine or an alkanolamine, more preferably a monoamine. Further, among the monoamines, alkylamines are particularly preferable.

  The carboxylic acid constituting the (A2) amine carboxylate may be either a monobasic acid or a polybasic acid.

  (A2) Among the carboxylic acids constituting the carboxylate of amine, the monobasic acid is usually a fatty acid having 2 to 24 carbon atoms, preferably a fatty acid having 6 to 20 carbon atoms, more preferably 8 to 18 carbon atoms. Fatty acids are used. The fatty acid may be linear or branched, but is preferably a linear fatty acid from the viewpoint of friction characteristics. The fatty acid may be either a saturated fatty acid or an unsaturated fatty acid, but a saturated fatty acid is preferable from the viewpoint of stability.

  Specific examples of the fatty acid having 2 to 25 carbon atoms include acetic acid, propionic acid, linear or branched butanoic acid, linear or branched pentanoic acid, linear or branched hexanoic acid, Linear or branched heptanoic acid, linear or branched octanoic acid, linear or branched nonanoic acid, linear or branched decanoic acid, linear or branched undecanoic acid, Linear or branched dodecanoic acid, linear or branched tridecanoic acid, linear or branched tetradecanoic acid, linear or branched pentadecanoic acid, linear or branched hexadecanoic acid, Linear or branched heptadecanoic acid, linear or branched octadecanoic acid, linear or branched hydroxyoctadecanoic acid, linear or branched nonadecanoic acid, linear or branched icosanoic acid Straight or branched helicosa Acid, linear or branched docosanoic acid, linear or branched tricosanoic acid, saturated fatty acid such as linear or branched tetracosanoic acid, acrylic acid, linear or branched butenoic acid, direct Linear or branched pentenoic acid, linear or branched hexenoic acid, linear or branched heptenoic acid, linear or branched octenoic acid, linear or branched nonenoic acid, direct Linear or branched decenoic acid, linear or branched undecenoic acid, linear or branched dodecenoic acid, linear or branched tridecenoic acid, linear or branched tetradecenoic acid, direct Linear or branched pentadecenoic acid, linear or branched hexadecenoic acid, linear or branched heptadecenoic acid, linear or branched octadecenoic acid, linear or branched hydroxyoctadecenoic acid Linear or branched nonadece Acid, linear or branched icosenoic acid, linear or branched henicosenoic acid, linear or branched docosenoic acid, linear or branched tricosenoic acid, linear or branched tetracosene Examples thereof include unsaturated fatty acids such as acids, and mixtures thereof.

  In addition, examples of the polybasic acid constituting the (A2) amine carboxylate include dibasic acid and trimellitic acid, and dibasic acid is preferable from the viewpoint of frictional characteristics. The dibasic acid may be a chain dibasic acid or a cyclic dibasic acid. Further, in the case of a chain dibasic acid, it may be either linear or branched, and may be either saturated or unsaturated. The chain dibasic acid is preferably a chain dibasic acid having 2 to 16 carbon atoms. Specifically, for example, ethanedioic acid, propanedioic acid, linear or branched butanedioic acid, linear Or branched pentanedioic acid, linear or branched hexanedioic acid, linear or branched heptanedioic acid, linear or branched octanedioic acid, linear or branched nonane diacid Acid, linear or branched decanedioic acid, linear or branched undecanedioic acid, linear or branched dodecanedioic acid, linear or branched tridecanedioic acid, linear or Branched tetradecanedioic acid, linear or branched heptadecanedioic acid, linear or branched hexadecanedioic acid, linear or branched hexenedioic acid, linear or branched heptenedioic acid Linear or branched octene diacid, linear or branched nonene diacid, linear or branched Branched decenedioic acid, linear or branched undecenedioic acid, linear or branched dodecenedioic acid, linear or branched tridecenedioic acid, linear or branched tetradecenedioic acid And linear or branched heptacene diacid, linear or branched hexadecene diacid, and mixtures thereof. Examples of the cyclic dibasic acid include 1,2-cyclohexanedicarboxylic acid, 4-cyclohexene-1,2-dicarboxylic acid, and aromatic dicarboxylic acid. Among these, a chain dibasic acid is preferable from the viewpoint of friction characteristics and stability.

  Among the carboxylic acids described above, monobasic acids are preferable from the viewpoint of friction characteristics.

  (A2) The carbon number of the amine carboxylate is not particularly limited, but from the viewpoint of frictional properties, the total carbon number of the amine and the carboxylic acid is preferably 8 to 60, and preferably 10 to 50. More preferably, it is 12-40.

Moreover, as (A3) amide, the amide represented by the following general formula (A-3) is preferable.
^{R 64 -CONH-R 65 (A} -3)

In the formula ^{(A-3), R 64} represents an alkenyl group of alkyl or C1-30 C1-30. R ⁶⁴ is preferably an alkyl group having 3 to 23 carbon atoms or an alkenyl group having 3 to 23 carbon atoms, more preferably an alkyl group having 5 to 18 carbon atoms or an alkenyl group having 5 to 18 carbon atoms. .

In the general formula (A-3), R ⁶⁵ represents a hydrogen atom, an alkanol group, an alkyl group having 1 to 30 carbon atoms, or an alkenyl group having 1 to 30 carbon atoms. R ⁶⁵ is preferably a hydrogen atom or an alkyl group, and most preferably a hydrogen atom. When R ⁶⁵ is an alkyl group, the alkyl group is preferably an alkyl group having 1 to 18 carbon atoms, more preferably an alkyl group having 1 to 12 carbon atoms, still more preferably an alkyl group having 1 to 8 carbon atoms, An alkyl group having 1 to 4 carbon atoms is more preferable, and an alkyl group having 1 or 2 carbon atoms is particularly preferable.

Moreover, in the amide represented by the general formula (A-3), the total carbon number of R ⁶⁴ and R ⁶⁵ is preferably 3 to 36, more preferably 5 to 28, from the viewpoint of friction characteristics. 7 to 24 is more preferable, and 11 to 18 is particularly preferable.

  In the present invention, among the above-mentioned nitrogen-containing oil-based agents, (A1) amine and (A3) amide are preferable, and (A1) amine is more preferable because a higher level of frictional properties can be obtained. Furthermore, among (A1) amines, monoamines and alkanolamines are preferable, and alkanolamines are more preferable.

  The content of the (A) nitrogen-containing oily agent in the refrigerator oil composition of the present invention is not particularly limited, but the content is 0.01% by mass or more based on the total amount of the composition from the viewpoint of friction characteristics. It is preferably 0.05% by mass or more, and more preferably 0.1% by mass or more. In addition, the content of the (A) nitrogen-containing oily agent is preferably 10% by mass or less, based on the total amount of the composition, from the point that the effect of reducing the friction coefficient commensurate with the content can be effectively obtained, and 7% by mass. % Or less is more preferable, and 5 mass% or less is still more preferable.

  The refrigerating machine oil composition of the present invention may be composed only of the above-mentioned lubricating base oil and nitrogen-containing oil-based agent, but for the purpose of further improving its various performances, various additives shown below are further included. Can be contained.

In the refrigerating machine oil composition of the present invention, it is preferable to blend (B) an epoxy compound in order to further improve its thermal / hydrolytic stability and frictional properties. (B) As a preferable example of an epoxy compound, the compound shown to the following (B1)-(B8) is mentioned.
(B1) Phenyl glycidyl ether type epoxy compound (B2) Alkyl glycidyl ether type epoxy compound (B3) Glycidyl ester type epoxy compound (B4) Allyloxirane compound (B5) Alkyloxirane compound (B6) Alicyclic epoxy compound (B7) Epoxy Fatty acid monoester (B8) epoxidized vegetable oil.

  Specific examples of the (B1) phenyl glycidyl ether type epoxy compound include phenyl glycidyl ether and alkylphenyl glycidyl ether. As used herein, the alkylphenyl glycidyl ether includes those having 1 to 3 alkyl groups having 1 to 13 carbon atoms, and those having one alkyl group having 4 to 10 carbon atoms, such as n-butylphenyl glycidyl. Ether, i-butylphenyl glycidyl ether, sec-butylphenyl glycidyl ether, tert-butylphenyl glycidyl ether, pentylphenyl glycidyl ether, hexylphenyl glycidyl ether, heptylphenyl glycidyl ether, octylphenyl glycidyl ether, nonylphenyl glycidyl ether, decylphenyl A glycidyl ether etc. can be illustrated as a preferable thing.

  (B2) As the alkyl glycidyl ether type epoxy compound, specifically, decyl glycidyl ether, undecyl glycidyl ether, dodecyl glycidyl ether, tridecyl glycidyl ether, tetradecyl glycidyl ether, 2-ethylhexyl glycidyl ether, neopentyl glycol di Examples thereof include glycidyl ether, trimethylolpropane triglycidyl ether, pentaerythritol tetraglycidyl ether, 1,6-hexanediol diglycidyl ether, sorbitol polyglycidyl ether, polyalkylene glycol monoglycidyl ether, polyalkylene glycol diglycidyl ether and the like.

  Specific examples of the (B3) glycidyl ester type epoxy compound include compounds represented by the following general formula (B-1).

［式中、Ｒ^６６は炭素数１〜１８の炭化水素基を表す］

[Wherein R ⁶⁶ represents a hydrocarbon group having 1 to 18 carbon atoms]

In the above formula (B-1), R ⁶⁶ represents a hydrocarbon group having 1 to 18 carbon atoms. Examples of such a hydrocarbon group include an alkyl group having 1 to 18 carbon atoms and an alkenyl group having 2 to 18 carbon atoms. Group, cycloalkyl group having 5 to 7 carbon atoms, alkyl cycloalkyl group having 6 to 18 carbon atoms, aryl group having 6 to 10 carbon atoms, alkylaryl group having 7 to 18 carbon atoms, arylalkyl having 7 to 18 carbon atoms Groups and the like. Among these, an alkylphenyl group having an alkyl group having 5 to 15 carbon atoms, an alkenyl group having 2 to 15 carbon atoms, a phenyl group, and an alkyl group having 1 to 4 carbon atoms is preferable.

  (B3) Among the glycidyl ester type epoxy compounds, preferred examples include glycidyl-2,2-dimethyloctanoate, glycidyl benzoate, glycidyl-tert-butyl benzoate, glycidyl acrylate, glycidyl methacrylate and the like. It can be illustrated.

  Specific examples of the (B4) allyloxirane compound include 1,2-epoxystyrene, alkyl-1,2-epoxystyrene, and the like.

  Specific examples of the (B5) alkyloxirane compound include 1,2-epoxybutane, 1,2-epoxypentane, 1,2-epoxyhexane, 1,2-epoxyheptane, 1,2-epoxyoctane, 1 , 2-epoxynonane, 1,2-epoxydecane, 1,2-epoxyundecane, 1,2-epoxydodecane, 1,2-epoxytridecane, 1,2-epoxytetradecane, 1,2-epoxypentadecane, 1, 2,2-epoxyhexadecane, 1,2-epoxyheptadecane, 1,1,2-epoxyoctadecane, 2-epoxynonadecane, 1,2-epoxyicosane and the like.

  (B6) As an alicyclic epoxy compound, the compound in which the carbon atom which comprises an epoxy group directly comprises the alicyclic ring like the compound represented by the following general formula (B-2) is mentioned. .

（Ｂ６）脂環式エポキシ化合物としては、具体的には、１，２−エポキシシクロヘキサン、１，２−エポキシシクロペンタン、３，４−エポキシシクロヘキシルメチル−３，４−エポキシシクロヘキサンカルボキシレート、ビス（３，４−エポキシシクロヘキシルメチル）アジペート、エキソ−２，３−エポキシノルボルナン、ビス（３，４−エポキシ−６−メチルシクロヘキシルメチル）アジペート、２−（７−オキサビシクロ［４．１．０］ヘプト−３−イル）−スピロ（１，３−ジオキサン−５，３‘−［７］オキサビシクロ［４．１．０］ヘプタン、４−（１‘−メチルエポキシエチル）−１，２−エポキシ−２−メチルシクロヘキサン、４−エポキシエチル−１，２−エポキシシクロヘキサン等が例示できる。

Specific examples of the (B6) alicyclic epoxy compound include 1,2-epoxycyclohexane, 1,2-epoxycyclopentane, 3,4-epoxycyclohexylmethyl-3,4-epoxycyclohexanecarboxylate, bis ( 3,4-epoxycyclohexylmethyl) adipate, exo-2,3-epoxynorbornane, bis (3,4-epoxy-6-methylcyclohexylmethyl) adipate, 2- (7-oxabicyclo [4.1.0] hept -3-yl) -spiro (1,3-dioxane-5,3 ′-[7] oxabicyclo [4.1.0] heptane, 4- (1′-methylepoxyethyl) -1,2-epoxy Examples thereof include 2-methylcyclohexane and 4-epoxyethyl-1,2-epoxycyclohexane.

  Specific examples of the (B7) epoxidized fatty acid monoester include esters of epoxidized fatty acids having 12 to 20 carbon atoms with alcohols or phenols having 1 to 8 carbon atoms and alkylphenols. In particular, butyl, hexyl, benzyl, cyclohexyl, methoxyethyl, octyl, phenyl and butylphenyl esters of epoxy stearate are preferably used.

  Specific examples of (B8) epoxidized vegetable oil include epoxy compounds of vegetable oils such as soybean oil, linseed oil, and cottonseed oil.

  As the (B) epoxy compound, one of the above components (B1) to (B8) may be used alone, or two or more may be used in combination. In the present invention, heat / hydrolysis stability and friction characteristics can be further improved, so that (B1) phenyl glycidyl ether type epoxy compound, (B3) glycidyl ester type epoxy compound, (B6) alicyclic epoxy compound (B7) Epoxidized fatty acid monoesters are preferred, (B3) glycidyl ester type epoxy compounds and (B6) alicyclic epoxy compounds are more preferred.

  (B) When the epoxy compound is blended in the refrigerating machine oil composition of the present invention, the blending amount is not particularly limited, but normally, the refrigerating machine oil composition is based on the total amount (based on the total amount of base oil and all blended additives). It is desirable to add an epoxy compound in such an amount that the content is 0.1 to 5.0% by mass, more preferably 0.2 to 2.0% by mass.

  Moreover, it is preferable that the refrigerating machine oil composition of this invention further contains (C) phosphorothionate from the point which can improve abrasion resistance further. As the phosphorothionate, a compound represented by the following general formula (C-1) is preferably used.

In the general formula (C-1), R ⁶⁷ , R ⁶⁸ and R ⁶⁹ may be the same or different and each represents a hydrocarbon group having 1 to 24 carbon atoms. Specific examples of the hydrocarbon group having 1 to 24 carbon atoms represented by R ^{67 to} R ⁶⁹ include an alkyl group, a cycloalkyl group, an alkenyl group, an alkylcycloalkyl group, an aryl group, an alkylaryl group, and an arylalkyl group. Etc.

  Examples of the alkyl group include methyl group, ethyl group, propyl group, butyl group, pentyl group, hexyl group, heptyl group, octyl group, nonyl group, decyl group, undecyl group, dodecyl group, tridecyl group, tetradecyl group, pentadecyl group. And alkyl groups such as hexadecyl group, heptadecyl group and octadecyl group (these alkyl groups may be linear or branched).

  As a cycloalkyl group, C5-C7 cycloalkyl groups, such as a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, can be mentioned, for example. Examples of the alkylcycloalkyl group include a methylcyclopentyl group, a dimethylcyclopentyl group, a methylethylcyclopentyl group, a diethylcyclopentyl group, a methylcyclohexyl group, a dimethylcyclohexyl group, a methylethylcyclohexyl group, a diethylcyclohexyl group, a methylcycloheptyl group, Examples thereof include an alkylcycloalkyl group having 6 to 11 carbon atoms such as a dimethylcycloheptyl group, a methylethylcycloheptyl group, and a diethylcycloheptyl group (the substitution position of the alkyl group with the cycloalkyl group is also arbitrary).

  Examples of the alkenyl group include butenyl, pentenyl, hexenyl, heptenyl, octenyl, nonenyl, decenyl, undecenyl, dodecenyl, tridecenyl, tetradecenyl, pentadecenyl, hexadecenyl, heptadecenyl, octadecenyl Alkenyl groups such as groups (these alkenyl groups may be linear or branched, and the position of the double bond is also optional).

  As an aryl group, aryl groups, such as a phenyl group and a naphthyl group, can be mentioned, for example. Examples of the alkylaryl group include tolyl group, xylyl group, ethylphenyl group, propylphenyl group, butylphenyl group, pentylphenyl group, hexylphenyl group, heptylphenyl group, octylphenyl group, nonylphenyl group, and decylphenyl. Group, an alkylaryl group having 7 to 18 carbon atoms such as undecylphenyl group and dodecylphenyl group (the alkyl group may be linear or branched, and the substitution position on the aryl group is arbitrary). .

  Examples of the arylalkyl group include arylalkyl groups having 7 to 12 carbon atoms such as benzyl group, phenylethyl group, phenylpropyl group, phenylbutyl group, phenylpentyl group, and phenylhexyl group (these alkyl groups may be linear or branched). May be branched).

A hydrocarbon group having a carbon number of 1 to 24 represented by the ^R 1 to R ³ is an alkyl group, an aryl group, preferably an alkyl aryl group, an alkyl group having 4 to 18 carbon atoms, having 7 to 24 carbon atoms An alkylaryl group and a phenyl group are more preferable.

  Specific examples of the phosphorothioate represented by the general formula (C-1) include tributyl phosphorothioate, tripentyl phosphorothioate, trihexyl phosphorothioate, triheptyl phosphorothioate, Trioctyl phosphorothioate, trinonyl phosphorothionate, tridecyl phosphorothionate, triundecyl phosphorothionate, tridodecyl phosphorothionate, tritridecyl phosphorothionate, tritetradecyl phosphorothionate , Tripentadecyl phosphorothionate, trihexadecyl phosphorothionate, triheptadecyl phosphorothionate, trioctadecyl phosphorothionate, trioleyl phosphorothionate, triphenyl phosphorothionate, Cresyl phosphorothioate, trixylenyl phosphorothioate, cresyl diphenyl phosphorothioate, xylenyl diphenyl phosphorothioate, tris (n-propylphenyl) phosphorothionate, tris (isopropylphenyl) phos Forothionate, tris (n-butylphenyl) phosphorothionate, tris (isobutylphenyl) phosphorothionate, tris (s-butylphenyl) phosphorothionate, tris (t-butylphenyl) phosphorothionate, etc. . Mixtures of these can also be used.

  The content of (C) phosphorothioate in the refrigerating machine oil composition of the present invention is preferably 0.01 to 5% by mass or less based on the total amount of the composition. By setting the content of phosphorothioate within the above range, the wear resistance and stability (particularly thermal / oxidative stability) of the refrigerating machine oil composition can be further improved. More specifically, the amount of phosphorothioate added is preferably 0.01% by mass or more, and more preferably 0.1% by mass or more from the viewpoint that a high level of wear resistance can be obtained. Further, even if the content is further increased, the effect of reducing wear corresponding to the content cannot be obtained, and on the contrary, it may cause the decrease in stability or the occurrence of corrosive wear. Preferably it is 5 mass% or less, More preferably, it is 3 mass% or less, More preferably, it is 1 mass% or less.

  The refrigerating machine oil composition of the present invention may further contain a phosphorus-based additive other than the phosphorothionate (hereinafter referred to as (D) a phosphorus-based additive). (D) The phosphorus-based additive includes at least one phosphorus compound selected from the group consisting of phosphate esters, acidic phosphate esters, amine salts of acidic phosphate esters, chlorinated phosphate esters, and phosphite esters. preferable. These phosphorus compounds are esters of phosphoric acid or phosphorous acid with alkanols and polyether type alcohols or derivatives thereof.

Phosphate esters include tributyl phosphate, tripentyl phosphate, trihexyl phosphate, triheptyl phosphate, trioctyl phosphate, trinonyl phosphate, tridecyl phosphate, triundecyl phosphate, tridodecyl phosphate, tritridecyl phosphate, tritetradecyl phosphate , Tripentadecyl phosphate, trihexadecyl phosphate, triheptadecyl phosphate, trioctadecyl phosphate, trioleyl phosphate, triphenyl phosphate, tricresyl phosphate, trixylenyl phosphate, cresyl diphenyl phosphate, xylenyl diphenyl phosphate, etc .;
Examples of acidic phosphate esters include monobutyl acid phosphate, monopentyl acid phosphate, monohexyl acid phosphate, monoheptyl acid phosphate, monooctyl acid phosphate, monononyl acid phosphate, monodecyl acid phosphate, monoundecyl acid phosphate, monododecyl Acid phosphate, monotridecyl acid phosphate, monotetradecyl acid phosphate, monopentadecyl acid phosphate, monohexadecyl acid phosphate, monoheptadecyl acid phosphate, monooctadecyl acid phosphate, monooleyl acid phosphate, dibutyl acid phosphate, dipentyl acid , Dihexyl reed Dophosphate, diheptyl acid phosphate, dioctyl acid phosphate, dinonyl acid phosphate, didecyl acid phosphate, diundecyl acid phosphate, didodecyl acid phosphate, ditridecyl acid phosphate, ditetradecyl acid phosphate, dipentadecyl acid, dipentadecyl acid Hexadecyl acid phosphate, diheptadecyl acid phosphate, dioctadecyl acid phosphate, dioleyl acid phosphate, etc .;
Examples of the amine salt of acidic phosphate ester include methylamine, ethylamine, propylamine, butylamine, pentylamine, hexylamine, heptylamine, octylamine, dimethylamine, diethylamine, dipropylamine, dibutylamine, Salts with amines such as dipentylamine, dihexylamine, diheptylamine, dioctylamine, trimethylamine, triethylamine, tripropylamine, tributylamine, tripentylamine, trihexylamine, triheptylamine, trioctylamine, etc .;
Examples of the chlorinated phosphate ester include tris-dichloropropyl phosphate, tris-chloroethyl phosphate, tris-chlorophenyl phosphate, polyoxyalkylene bis [di (chloroalkyl)] phosphate, and the like;
As phosphites, dibutyl phosphite, dipentyl phosphite, dihexyl phosphite, diheptyl phosphite, dioctyl phosphite, dinonyl phosphite, didecyl phosphite, diundecyl phosphite, didodecyl phosphite, dioleyl Phosphite, diphenyl phosphite, dicresyl phosphite, tributyl phosphite, tripentyl phosphite, trihexyl phosphite, triheptyl phosphite, trioctyl phosphite, trinonyl phosphite, tridecyl phosphite, triundecyl phosphite Phyto, tridodecyl phosphite, trioleyl phosphite, triphenyl phosphite, tricresyl phosphite and the like. Mixtures of these can also be used.

  The content of the phosphorus additive (D) in the refrigerating machine oil composition of the present invention is preferably 0.01 to 5% by mass or less based on the total amount of the composition. By setting the content of the ester-based additive within the above range, the wear resistance and stability (particularly thermal / oxidative stability) can be further improved. More specifically, the addition amount of the phosphorus-based additive is preferably 0.01% by mass or more, more preferably 0.1% by mass or more from the viewpoint that a high level of wear resistance can be obtained. Further, even if the content is further increased, the effect of reducing wear corresponding to the content cannot be obtained, and on the contrary, it may cause the decrease in stability or the occurrence of corrosion wear. Although it is 5 mass% or less, Preferably it is 4 mass% or less, More preferably, it is 3 mass% or less.

  Moreover, it is preferable that the refrigerating machine oil composition of this invention further contains (E) benzotriazole and / or its derivative (s). Inclusion of benzotriazole and / or a derivative thereof can further enhance the effect of improving wear resistance and friction characteristics.

  Benzotriazole is a compound represented by the following formula (E-1).

  Examples of the benzotriazole derivative include alkylbenzotriazole represented by the following general formula (E-2) and (alkyl) aminoalkylbenzotriazole represented by the following general formula (E-3). .

In the above formula (E-2), R ⁷⁰ represents a linear or branched alkyl group having 1 to 4 carbon atoms, preferably a methyl group or an ethyl group, and x is 1 to 3, preferably 1 Or the number of 2 is shown. Examples of R ⁶¹ include a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, an isobutyl group, a sec-butyl group, and a tert-butyl group. As the alkylbenzotriazole represented by the general formula (14), a compound in which R ⁷⁰ is a methyl group or an ethyl group and x is 1 or 2 is particularly preferable from the viewpoint of excellent antioxidant properties. Examples thereof include benzotriazole (tolyltriazole), dimethylbenzotriazole, ethylbenzotriazole, ethylmethylbenzotriazole, diethylbenzotriazole, and mixtures thereof.

In the formula (E-2), R ⁷¹ is a linear or branched alkyl group having 1 to 4 carbon atoms, preferably methyl or ethyl group, R ⁷² represents a methylene group or an ethylene group, R ⁷³ and R ⁷⁴ may be the same or different, and are a hydrogen atom or a linear or branched alkyl group having 1 to 18 carbon atoms, preferably a linear or branched group having 1 to 12 carbon atoms. Represents an alkyl group, and y represents a number of 0 to 3, preferably 0 or 1. Examples of R ⁷¹ include a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, an isobutyl group, a sec-butyl group, and a tert-butyl group. As R ⁷³ and R ⁷⁴ , for example, a hydrogen atom, methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, isobutyl group, sec-butyl group, tert-butyl group, straight chain or A branched pentyl group, a linear or branched hexyl group, a linear or branched heptyl group, a linear or branched octyl group, a linear or branched nonyl group, a linear or branched decyl group, Linear or branched undecyl group, linear or branched dodecyl group, linear or branched tridecyl group, linear or branched tetradecyl group, linear or branched pentadecyl group, linear or branched Alkyl groups such as a hexadecyl group, a linear or branched heptadecyl group, and a linear or branched octadecyl group.

As the (alkyl) aminobenzotriazole represented by the above formula (E-3), R ⁷¹ is a methyl group, y is 0 or 1, and R ⁷² is methylene because it is particularly excellent in antioxidant properties. A dialkylaminoalkylbenzotriazole, dialkylaminoalkyltolyltriazole or a mixture thereof, which is a group or an ethylene group, and R ⁷³ and R ⁷⁴ are linear or branched alkyl groups having 1 to 12 carbon atoms, are preferably used. It is done. Examples of these dialkylaminoalkylbenzotriazoles include dimethylaminomethylbenzotriazole, diethylaminomethylbenzotriazole, di (linear or branched) propylaminomethylbenzotriazole, and di (linear or branched) butylaminomethylbenzotriazole. , Di (straight or branched) pentylaminomethylbenzotriazole, di (straight or branched) hexylaminomethylbenzotriazole, di (straight or branched) heptylaminomethylbenzotriazole, di (straight or branched) ) Octylaminomethylbenzotriazole, di (straight or branched) nonylaminomethylbenzotriazole, di (straight or branched) decylaminomethylbenzotriazole, di (straight or branched) undecylaminomethylbenzotriazole, (Linear or branched) dodecylaminomethylbenzotriazole; dimethylaminoethylbenzotriazole, diethylaminoethylbenzotriazole, di (linear or branched) propylaminoethylbenzotriazole, di (linear or branched) butylaminoethylbenzo Triazole, di (straight or branched) pentylaminoethylbenzotriazole, di (straight or branched) hexylaminoethylbenzotriazole, di (straight or branched) heptylaminoethylbenzotriazole, di (straight or branched) Branch) Octylaminoethylbenzotriazole, Di (straight or branched) nonylaminoethylbenzotriazole, Di (straight or branched) decylaminoethylbenzotriazole, Di (straight or branched) undecylaminoethylbenzotriazole , Di (linear or straight Branched) dodecylaminoethyl benzotriazole; dimethylaminomethyltolyltriazole, diethylaminomethyltolyltriazole, di (linear or branched) propylaminomethyltolyltriazole, di (straight or branched) butylaminomethyltolyltriazole, di ( Linear or branched) pentylaminomethyltolyltriazole, di (linear or branched) hexylaminomethyltolyltriazole, di (straight or branched) heptylaminomethyltolyltriazole, di (linear or branched) octylamino Methyltolyltriazole, di (linear or branched) nonylaminomethyltolyltriazole, di (straight or branched) decylaminomethyltolyltriazole, di (straight or branched) undecylaminomethyltolyltriazole, di (direct Chain or branch) Silaminomethyltolyltriazole; dimethylaminoethyltolyltriazole, diethylaminoethyltolyltriazole, di (linear or branched) propylaminoethyltolyltriazole, di (linear or branched) butylaminoethyltolyltriazole, di (linear or Branched) pentylaminoethyltolyltriazole, di (straight or branched) hexylaminoethyltolyltriazole, di (straight or branched) heptylaminoethyltolyltriazole, di (straight or branched) octylaminoethyltolyltriazole , Di (linear or branched) nonylaminoethyl tolyl triazole, di (linear or branched) decylaminoethyl tolyl triazole, di (linear or branched) undecylaminoethyl tolyl triazole, di (linear or branched) Branch) Dodecylamino Tilt Lil triazole; or mixtures thereof.

  The content of (E) benzotriazole and / or its derivative in the refrigerating machine oil composition of the present invention is arbitrary, but is preferably 0.001% by mass or more, more preferably 0.005% by mass, based on the total amount of the composition. That's it. When the amount is less than 0.001% by mass, the effect of improving wear resistance and frictional properties due to the inclusion of benzotriazole and / or its derivatives may be insufficient. Further, the content of benzotriazole and / or its derivative is preferably 1.0% by mass or less, more preferably 0.5% by mass or less, based on the total amount of the composition. If it exceeds 1.0% by mass, the effect of improving the wear resistance and frictional properties corresponding to the content cannot be obtained, which may be economically disadvantageous.

  The refrigerating machine oil composition of the present invention may further contain an oily agent other than the nitrogen-containing oily agent (hereinafter referred to as “(F) other oily agent”). (F) Other oil agents include (F1) ester oil agents, (F2) monohydric alcohol oil agents, (F3) carboxylic acid oil agents, (F4) ether oil agents, and the like.

  (F1) The ester oily agent may be a natural product (usually contained in natural fats and oils derived from animals and plants) or a synthetic product. In this invention, it is preferable that it is a synthetic ester from points, such as stability of the refrigerator oil composition obtained, and the uniformity of an ester component.

  (F1) A synthetic ester as an ester oily agent is obtained by reacting an alcohol and a carboxylic acid. The alcohol may be a monohydric alcohol or a polyhydric alcohol. The carboxylic acid may be a monobasic acid or a polybasic acid.

  (F1) As the monohydric alcohol constituting the ester oily agent, those having 1 to 24 carbon atoms, preferably 1 to 12 carbon atoms, more preferably 1 to 8 carbon atoms are usually used. However, it may be branched, and may be saturated or unsaturated. Moreover, as a polyhydric alcohol which comprises (F1) ester oiliness agent, a 2-10 valence normally, Preferably a 2-6 valence thing is used.

  Among the acids constituting the (F1) ester oily agent, as the monobasic acid, a fatty acid having 2 to 24 carbon atoms is usually used, and the fatty acid may be linear or branched and saturated. Or unsaturated. Examples of the basic acid include dibasic acid and trimellitic acid, and dibasic acid is preferred from the viewpoint of preventing precipitation under a refrigerant atmosphere and at a low temperature. The dibasic acid may be a chain dibasic acid or a cyclic dibasic acid. Further, in the case of a chain dibasic acid, it may be either linear or branched, and may be either saturated or unsaturated. As the chain dibasic acid, a chain dibasic acid having 2 to 16 carbon atoms is preferable.

  (F1) The acid constituting the ester oily agent may be a monobasic acid or a polybasic acid as described above, but from the point that the effect of improving wear resistance and friction properties is more excellent, Basic acids are preferred.

The combination of the alcohol and the acid in the ester oily agent is arbitrary and not particularly limited, and examples thereof include esters by combinations of the following (F1-1) to (F1-7).
(F1-1) ester of monohydric alcohol and monobasic acid (F1-2) ester of polyhydric alcohol and monobasic acid (F1-3) ester of monohydric alcohol and polybasic acid (F1-4) Ester of polyhydric alcohol and polybasic acid (F1-5) Monohydric alcohol, Mixture of polyhydric alcohol and polybasic acid (F1-6) Polyhydric alcohol and monobasic acid, polybasic acid Mixed ester (F1-7) with monohydric alcohol, polyhydric alcohol, monobasic acid, and polybasic acid.

  Examples of the (F2) monohydric alcohol oil-based agent include the monohydric alcohols described in the description of the (F1) ester oil-based agent. The total number of carbon atoms of the monohydric alcohol oil-based agent is preferably 6 or more, more preferably 8 or more, and most preferably 10 or more, from the viewpoint of improving frictional characteristics and wear characteristics. Moreover, since there exists a possibility that it may become easy to precipitate in a refrigerant | coolant atmosphere when a total carbon number is too large, 20 or less are preferable, 18 or less are more preferable, and 16 or less are the most preferable.

  Further, the (F3) carboxylic acid oily agent may be a monobasic acid or a polybasic acid. Examples of such carboxylic acids include monobasic acids and polybasic acids described in the description of the (F1) ester oily agent. Among these, monobasic acids are preferable from the viewpoint of improving frictional characteristics and wear characteristics. In addition, the total number of carbon atoms of the carboxylic acid oil-based agent is preferably 6 or more, more preferably 8 or more, and most preferably 10 or more, from the viewpoint of improving frictional characteristics and wear characteristics. Moreover, since there exists a possibility that it may precipitate easily in a refrigerant | coolant atmosphere when the total carbon number of a carboxylic acid oiliness agent is too large, 20 or less are preferable, 18 or less are more preferable, and 16 or less are the most preferable.

  Examples of the (F4) ether oil agent include etherified products of 3-6 valent aliphatic polyhydric alcohols, bimolecular condensates or trimolecular condensates of 3-6 valent aliphatic polyhydric alcohols, and the like. Among them, diphenyl octyl triether of glycerin, di (methyloxyisopropylene) dodecyl triether of trimethylolpropane, tetrahexyl ether of pentaerythritol, hexapropyl ether of sorbitol, dimethyldioctyl tetraether of diglycerin, triglycerin Tetra (methyloxyisopropylene) decyl pentaether, hexapentyl ether of dipentaerythritol, and pentamethyloctyl hexaether of tripentaerythritol are preferably used.

  In the refrigerating machine oil composition of the present invention, one of (F1) ester oil agent, (F2) monohydric alcohol oil agent, (F3) carboxylic acid oil agent and (F4) ether oil agent is used alone. It may also be used in combination of two or more. Among these oily agents, (F1) ester oily agents are preferable because they can achieve friction properties, wear properties, precipitation prevention properties, and stability at a high level in a well-balanced manner. (F1) Ester oil agent not only achieves high wear resistance and friction properties, but also has better anti-precipitation properties than (F2) monohydric alcohol oil agent and (F4) ether oil agent. In addition, (F3) is more stable than carboxylic acid oil.

  The content of the (F) other oily agent in the refrigerating machine oil composition of the present invention is arbitrary, but preferably 0.01% based on the total amount of the composition from the viewpoint of excellent effect of improving wear resistance and friction characteristics. It is at least mass%, more preferably at least 0.05 mass%, still more preferably at least 0.1 mass%. In addition, the content is preferably 10% by mass or less, based on the total amount of the composition, from the viewpoint of excellent precipitation prevention under a refrigerant atmosphere and low temperature, and heat / oxidation stability of the refrigerating machine oil composition. Preferably it is 7.5 mass% or less, More preferably, it is 5 mass% or less.

  Furthermore, in order to further improve the performance of the refrigerating machine oil composition in the present invention, a conventionally known refrigerating machine oil additive such as di-tert-butyl-p-cresol, bisphenol A or other phenolic type is used as necessary. Antioxidants, amine-based antioxidants such as phenyl-α-naphthylamine, N, N-di (2-naphthyl) -p-phenylenediamine, antiwear agents such as zinc dithiophosphate, chlorinated paraffin, sulfur compounds, etc. These extreme pressure agents, silicone-based antifoaming agents, viscosity index improvers, pour point depressants, cleaning dispersants, and other additives can be used alone or in combination. The total blending amount of these additives is not particularly limited, but is preferably 10% by mass or less, more preferably 5% by mass or less on the basis of the total amount of the refrigerating machine oil composition (based on the total amount of the base oil and all the blending additives). .

The volume resistivity of the refrigerator oil composition of the present invention is not particularly limited, but is preferably 1.0 × 10 ⁹ Ω · cm or more. In particular, high electrical insulation tends to be required when used in a closed refrigerator. Here, the volume resistivity means a value [Ω · cm] at 25 ° C. measured in accordance with JIS C 2101 “Electrical Insulating Oil Test Method”.

  Furthermore, although the water content of the refrigerating machine oil composition of the present invention is not particularly limited, it is preferably 200 ppm or less, more preferably 100 ppm or less, and most preferably 50 ppm or less, based on the total amount of the refrigerating machine oil composition. In particular, when used for a closed type refrigerator, the water content is required to be low from the viewpoint of the influence on the heat and hydrolysis stability of oil and electrical insulation.

  Furthermore, the acid value of the refrigerating machine oil composition of the present invention is not particularly limited, but is preferably 0.1 mgKOH / g or less, more preferably 0 in order to prevent corrosion to the metal used in the refrigerating machine or piping. 0.05 mgKOH / g or less. The acid value here means a value [mg KOH / g] measured in accordance with JIS K 2501 “Petroleum products and lubricating oil-neutralization number test method”.

  Furthermore, the ash content of the refrigerating machine oil composition of the present invention is not particularly limited, but is preferably 100 ppm or less, more preferably, in order to increase the heat / hydrolysis stability of the refrigerating machine oil composition of the present invention and suppress the generation of sludge and the like. Can be 50 ppm or less. In the present invention, ash means a value [ppm] measured in accordance with JIS K 2272 “Testing method for ash and sulfated ash of crude oil and petroleum products”.

  Refrigerants used in the refrigerator using the refrigerator oil composition of the present invention include HFC refrigerants, fluorine-containing ether refrigerants such as perfluoroethers, non-fluorine-containing ether refrigerants such as dimethyl ether, carbon dioxide, ammonia, hydrocarbons, etc. These natural refrigerants may be used alone or as a mixture of two or more.

  Examples of the HFC refrigerant include hydrofluorocarbons having 1 to 3 carbon atoms, preferably 1 to 2 carbon atoms. Specifically, for example, difluoromethane (HFC-32), trifluoromethane (HFC-23), pentafluoroethane (HFC-125), 1,1,2,2-tetrafluoroethane (HFC-134), 1, HFC such as 1,1,2-tetrafluoroethane (HFC-134a), 1,1,1-trifluoroethane (HFC-143a), 1,1-difluoroethane (HFC-152a), or two or more of these And the like. These refrigerants are appropriately selected depending on the application and required performance. For example, HFC-32 alone; HFC-23 alone; HFC-134a alone; HFC-125 alone; HFC-134a / HFC-32 = 60 to 80 mass % / 40-20 mass% mixture; HFC-32 / HFC-125 = 40-70 mass% / 60-30 mass% mixture; HFC-125 / HFC-143a = 40-60 mass% / 60-40 mass % Mixture; HFC-134a / HFC-32 / HFC-125 = 60 wt% / 30 wt% / 10 wt% mixture; HFC-134a / HFC-32 / HFC-125 = 40-70 wt% / 15- 35 mass% / 5 to 40 mass% mixture; HFC-125 / HFC-134a / HFC-143a = 35-55 mass% / 1-15 mass% / 40-60 mass Mixtures of preferred examples include. More specifically, a mixture of HFC-134a / HFC-32 = 70/30 mass%; a mixture of HFC-32 / HFC-125 = 60/40 mass%; HFC-32 / HFC-125 = 50/50 mass % Mixture (R410A); HFC-32 / HFC-125 = 45/55 wt% mixture (R410B); HFC-125 / HFC-143a = 50/50 wt% mixture (R507C); HFC-32 / HFC -125 / HFC-134a = 30/10/60 wt% mixture; HFC-32 / HFC-125 / HFC-134a = 23/25/52 wt% mixture (R407C); HFC-32 / HFC-125 / HFC-134a = 25/15/60 mass% mixture (R407E); HFC-125 / HFC-134a / HFC-143a = Mixtures of 4/4/52 wt% (R404A), and the like.

  Examples of natural refrigerants include carbon dioxide, ammonia, and hydrocarbons. Here, the hydrocarbon refrigerant is preferably a gas at 25 ° C. and 1 atm. Specifically, it is an alkane, cycloalkane, alkene or a mixture thereof having 1 to 5 carbon atoms, preferably 1 to 4 carbon atoms. Specific examples include methane, ethylene, ethane, propylene, propane, cyclopropane, butane, isobutane, cyclobutane, methylcyclopropane, or a mixture of two or more thereof. Among these, propane, butane, isobutane or a mixture thereof is preferable.

  The refrigerating machine oil composition of the present invention is usually present in the form of a refrigerating machine fluid composition mixed with the refrigerant as described above in the refrigerating machine. The blending ratio of the refrigerating machine oil and the refrigerant in this fluid composition is not particularly limited, but the refrigerating machine oil is preferably 1 to 500 parts by weight, more preferably 2 to 400 parts by weight with respect to 100 parts by weight of the refrigerant.

  The refrigerating machine oil composition of the present invention can sufficiently reduce both the static friction coefficient and the dynamic friction coefficient in the sliding portion of the refrigerant compressor or the like, and sufficiently reduces both the starting power and the power consumption during operation. Therefore, it is very useful in achieving a high level of energy saving. The refrigerating and air-conditioning equipment in which the refrigerating machine oil composition of the present invention is used is not particularly limited, and is suitably used for a refrigerating equipment or a heat pump having a reciprocating or rotating open type, semi-hermetic or hermetic compressor. be able to. More specifically, such refrigeration equipment includes automotive air conditioners, dehumidifiers, refrigerators, refrigerated warehouses, vending machines, showcases, cooling equipment for chemical plants, residential air conditioners, packaged air conditioners, heat pumps for hot water supply, etc. Can be mentioned. Furthermore, the refrigerating machine oil composition of the present invention can be used in any type of compressor such as a reciprocating type, a rotary type, and a centrifugal type.

  As a configuration of a refrigerant circulation system in which the refrigerating machine oil composition of the present invention can be suitably used, typically, a refrigerant compressor, a condenser, an expansion mechanism, and an evaporator are connected in this order via respective flow paths. Examples thereof include a dryer provided in the flow path as necessary.

  As a refrigerant compressor, a motor composed of a rotor and a stator in a sealed container for storing refrigerating machine oil, a rotating shaft fitted to the rotor, and a compressor connected to the motor via the rotating shaft A high-pressure container type compressor in which high-pressure refrigerant gas discharged from the compressor unit stays in a sealed container, a motor composed of a rotor and a stator in a sealed container storing refrigerating machine oil, and rotation A low pressure in which a rotating shaft fitted to the child and a compressor unit connected to the motor via the rotating shaft are housed, and high-pressure refrigerant gas discharged from the compressor unit is directly discharged out of the sealed container Examples thereof include a container type compressor.

  As an insulating film which is an electric insulation system material of a motor part, a crystalline plastic film having a glass transition point of 50 ° C. or more, specifically, for example, polyethylene terephthalate, polybutylene terephthalate, polyphenylene sulfide, polyether ether ketone, polyethylene naphthalate, Polyamideimide, at least one insulating film selected from the group of polyimides, or a composite film in which a resin layer having a high glass transition temperature is coated on a film having a low glass transition temperature is less likely to cause deterioration of tensile strength characteristics and electrical insulation characteristics. Are preferably used. In addition, as a magnet wire used in the motor unit, an enamel coating having a glass transition temperature of 120 ° C. or higher, for example, a single layer such as polyester, polyesterimide, polyamide and polyamideimide, or a layer having a low glass transition temperature as a lower layer, Those having an enamel coating in which a high layer is composite-coated on the upper layer are preferably used. Examples of the composite enameled wire include polyester imide as a lower layer and polyamide imide as an upper layer (AI / EI), polyester as a lower layer and polyamide imide as an upper layer (AI / PE), and the like. .

  As the desiccant to be filled in the dryer, silicic acid and alkali metal aluminate composite salt having a pore diameter of 3.3 angstroms or less and a carbon dioxide absorption capacity at 25 ° C. carbon dioxide partial pressure of 250 mmHg is 1.0% or less. The synthetic zeolite is preferably used. Specifically, trade names XH-9, XH-10, XH-11, XH-600 manufactured by Union Showa Co., Ltd., and the like can be given.

  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 54, Comparative Examples 1 to 11]
In Examples 1 to 54 and Comparative Examples 1 to 11, refrigerator oil compositions having the compositions shown in Tables 1 to 9 were prepared using the base oils and additives shown below, respectively.
(Base oil)
Base oil 1: tetraester of pentaerythritol, equimolar mixture of 2-ethylhexanoic acid and 3,5,5-trimethylhexanoic acid (kinematic viscosity at 40 ° C .: 68.5 mm ² /
s, pour point: −25 ° C.)
Base oil 2: diester of 1,2-cyclohexanedicarboxylic acid and 2-ethylhexanol (kinematic viscosity at 40 ° C .: 15 mm ² / s, pour point: −40 ° C.)
Base oil 3: Random copolymer of vinyl ethyl ether and vinyl isobutyl ether (molar ratio of vinyl ethyl ether to vinyl isobutyl ether: 7/1, number average molecular weight: 900, kinematic viscosity at 40 ° C .: 68.5 mm ² / S, kinematic viscosity at 100 ° C .: 8 mm ² / s, pour point: −40 ° C.)
Base oil 4: Naphthenic mineral oil (kinematic viscosity at 40 ° C .: 56.6 mm ² / s, pour point: −3
0 ℃)
Base oil 5: Polypropylene glycol monomethyl ether (number average molecular weight: 1000, kinematic viscosity at 40 ° C .: 46 mm ² / s, kinematic viscosity at 100 ° C .: 10 mm ² / s, pour point: −40 ° C.)
Base oil 6: linear alkylbenzene (kinematic viscosity at 40 ° C. 27 mm ² / s, pour point −45 ° C. or lower)
Base oil 7: highly refined paraffinic mineral oil (kinematic viscosity at 40 ° C. 12 mm ² / s, pour point −20 ° C.)
Base oil 8: highly refined paraffinic mineral oil (kinematic viscosity at 40 ° C. 96 mm ² / s, pour point −17.5 ° C.)
(Nitrogen-containing oil-based agent)
A1: Octyl (dimethyl) amine A2: Stearyl (dimethyl) amine A3: Tetracosylamine A4: Octyl diethanolamine A5: Stearyl diethanolamine A6: Tetracosyl diethanolamine A7: Octanoic acid amide (amide of octanoic acid and ammonia)
A8: Oleic acid amide (amide of oleic acid and ammonia)
A9: Tetracosanoic acid amide (amide of tetracosanoic acid and ammonia)
(Nitrogen-containing additive for comparison)
B1: benzotriazole B2: N-octylbenzotriazole B3: thiadiazole (other additives)
C1: Glycidyl-2,2′-dimethyloctanoate C2: Triphenyl phosphorothioate C3: Tricresyl phosphate C4: Butyl stearate

  Next, the following evaluation was performed about each refrigeration oil composition of Examples 1-54 and Comparative Examples 1-11.

[Frictional property evaluation test]
A sliding part of a Falex testing machine (ASTM D2714) was installed in a pressure resistant container, a refrigerant was introduced into the container, and a FALEX test was performed under the following conditions. The friction coefficient for 2 minutes from the start of the test was measured at 10 points per second (every 0.1 second), and divided by the number of measurement points to evaluate as a static friction coefficient. Further, the test was continued for 30 minutes thereafter, and the average value of the friction coefficient for 28 minutes, excluding the initial value of the friction coefficient for 2 minutes, was evaluated as the dynamic friction coefficient. The obtained results are shown in Tables 1-9.
Test material: Steel ring, steel block test start temperature: 80 ° C
Test time: 60 minutes Sliding speed: 0.5 m / s
Load: 500N.

Claims (1)

A predetermined lubricating base oil,
A refrigerating machine oil composition comprising at least one nitrogen-containing oily agent selected from amines, amine carboxylates and amides.