JPH0517794A - Lubricant composition - Google Patents

Lubricant composition

Info

Publication number
JPH0517794A
JPH0517794A JP3176555A JP17655591A JPH0517794A JP H0517794 A JPH0517794 A JP H0517794A JP 3176555 A JP3176555 A JP 3176555A JP 17655591 A JP17655591 A JP 17655591A JP H0517794 A JPH0517794 A JP H0517794A
Authority
JP
Japan
Prior art keywords
group
carbon atoms
hydrogen
aryl
cycloalkyl
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP3176555A
Other languages
Japanese (ja)
Other versions
JP2966975B2 (en
Inventor
Katsumi Hashimoto
勝美 橋本
Takamichi Seiki
啓通 清木
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Idemitsu Kosan Co Ltd
Original Assignee
Idemitsu Kosan Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Idemitsu Kosan Co Ltd filed Critical Idemitsu Kosan Co Ltd
Priority to JP3176555A priority Critical patent/JP2966975B2/en
Priority to EP92111780A priority patent/EP0523561A1/en
Priority to KR1019920012862A priority patent/KR930002490A/en
Publication of JPH0517794A publication Critical patent/JPH0517794A/en
Application granted granted Critical
Publication of JP2966975B2 publication Critical patent/JP2966975B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M169/00Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
    • C10M169/04Mixtures of base-materials and additives
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    • C10M107/00Lubricating compositions characterised by the base-material being a macromolecular compound
    • C10M107/48Lubricating compositions characterised by the base-material being a macromolecular compound containing phosphorus
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    • C10M105/00Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
    • C10M105/08Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen
    • C10M105/32Esters
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    • C10M105/00Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
    • C10M105/08Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen
    • C10M105/32Esters
    • C10M105/36Esters of polycarboxylic acids
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    • C10M105/00Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
    • C10M105/08Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen
    • C10M105/32Esters
    • C10M105/38Esters of polyhydroxy compounds
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    • C10M133/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
    • C10M133/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms
    • C10M133/04Amines, e.g. polyalkylene polyamines; Quaternary amines
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    • C10M133/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
    • C10M133/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms
    • C10M133/04Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M133/06Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
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    • C10M137/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus
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    • C10M137/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus
    • C10M137/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus having no phosphorus-to-carbon bond
    • C10M137/04Phosphate esters
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    • C10M171/00Lubricating compositions characterised by purely physical criteria, e.g. containing as base-material, thickener or additive, ingredients which are characterised exclusively by their numerically specified physical properties, i.e. containing ingredients which are physically well-defined but for which the chemical nature is either unspecified or only very vaguely indicated
    • C10M171/008Lubricant compositions compatible with refrigerants
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
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    • C10M2207/2805Esters used as base material
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    • C10M2207/282Esters of (cyclo)aliphatic oolycarboxylic acids
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    • C10M2207/28Esters
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    • C10M2207/2825Esters of (cyclo)aliphatic oolycarboxylic acids used as base material
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
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    • C10M2207/2855Esters of aromatic polycarboxylic acids used as base material
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    • C10M2211/02Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen and halogen only
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    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/40Generators or electric motors in oil or gas winning field
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/42Flashing oils or marking oils
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/44Super vacuum or supercritical use
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/50Medical uses

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Abstract

PURPOSE:To obtain a lubricant composition excellent in abrasion resistance and hydrolysis resistance by blending a base oil mainly composed of an ester- based compound with a specified phosphorus-based compound and an amine compound. CONSTITUTION:A lubricant composition obtained by blending (A) a base oil mainly composed of an ester-based compound such as trimethylolpropane tert-2- ethylhexanoate, pentaerythritol tetra-2-ethylhexanoate or dioctyl adipate with (B) a phosphorus-based compound of formula I, II or III [R<1> and R<2> are 3-30C (cyclo)alkyl or 6-30C aryl; R<3>-R<5>, R<9>, R<10>, R<12> and R<13> are H or 3-30C (cyclo) or 6-30C aryl; R<6>-R<8> and R'' are 2-4C alkylene;), (q) and (r) are 0-2; X is 1-20], e.g. dilaurylhydrogen phosphite and (C) an amine compound of formula IV (R<14>-R<16> are same as the above-mentioned R<3>) e.g. cyclohexyldodecylamine.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は潤滑油組成物に関し、詳
しくは、エステル系化合物を主成分とする基油に、特定
のリン系化合物及びアミン化合物を配合し、耐摩耗性及
び耐加水分解性の優れた潤滑油組成物に関するものであ
る。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a lubricating oil composition, and more specifically, to a base oil containing an ester compound as a main component, a specific phosphorus compound and an amine compound are blended to obtain abrasion resistance and hydrolysis resistance. The present invention relates to a lubricating oil composition having excellent properties.

【0002】[0002]

【従来の技術及び発明が解決しようとする課題】従来、
潤滑油としては、鉱油からなる鉱物性潤滑油,化学的に
合成した合成潤滑油,動植物系油脂からなる脂肪性潤滑
油及び鉱油と動植物油脂とを混合した混成潤滑油並びに
鉱油と合成油とを混合した混成潤滑油など各種のものが
使用されている。これらの中では、化学的に種々に変性
合成ができる合成潤滑油の使用が増加しており、特に、
エステル系の潤滑油は多岐のわたっている。しかるに、
エステル系の潤滑油は、エステル単体では耐摩耗性が悪
く、冷凍機用圧縮機に使用した場合にも摺動部材の摩耗
が著しい欠点を有する。それを防止するために摩耗防止
剤として、通常、トリクレジルホスフェート(TCP)
やトリフェニルホスファイト(TPP)等が使用されて
いるが、その摩耗防止効果は期待される程のものはな
い。そして、エステルは、水の存在下で加水分解を受け
やすく、脂肪酸や脂肪酸金属塩が生成して系内の腐食や
毛細管の目詰りを惹起する欠点がある。
2. Description of the Related Art Conventionally, the problems to be solved by the invention
As the lubricating oil, a mineral lubricating oil made of mineral oil, a chemically synthesized synthetic lubricating oil, a fatty lubricating oil made of animal and vegetable fats and oils, and a mixed lubricating oil made by mixing mineral oil and animal and vegetable fats and oils and synthetic oils are used. Various things such as mixed mixed lubricating oil are used. Among these, the use of synthetic lubricating oils that can be chemically modified in various ways is increasing, and in particular,
A wide variety of ester-based lubricating oils are available. However,
Ester-based lubricating oils have poor wear resistance when used alone as an ester, and have a drawback that the sliding members are significantly worn even when used in a compressor for a refrigerator. As an antiwear agent to prevent it, tricresyl phosphate (TCP) is usually used.
Although triphenyl phosphite (TPP) and the like are used, their anti-wear effect is not as high as expected. Further, the ester is susceptible to hydrolysis in the presence of water, and has a drawback that a fatty acid or a fatty acid metal salt is formed to cause corrosion in the system and clogging of capillaries.

【0003】[0003]

【課題を解決するための手段】そこで、本発明者らは、
上記状況を鑑み、エステル系化合物を主成分とする基油
について、より性能の優れた潤滑油を得るべく鋭意検討
を重ねた。その結果、特定のリン系化合物及びアミン化
合物を配合することによって、上記目的を達成できるこ
とを見出した。本発明はかかる知見に基いて完成したも
のである。
Therefore, the present inventors have
In view of the above situation, the base oil containing an ester compound as a main component has been earnestly studied in order to obtain a lubricating oil having more excellent performance. As a result, they have found that the above object can be achieved by blending a specific phosphorus compound and an amine compound. The present invention has been completed based on such findings.

【0004】すなわち、本発明は、(A)エステル系化
合物を主成分とする基油,(B)一般式(I),(II)
あるいは(III)
That is, the present invention provides (A) a base oil containing an ester compound as a main component, (B) general formulas (I) and (II).
Or (III)

【0005】[0005]

【化5】 [Chemical 5]

【0006】[0006]

【化6】 [Chemical 6]

【0007】[0007]

【化7】 [Chemical 7]

【0008】〔式中、R1 及びR2 はそれぞれ炭素数3
〜30のアルキル基,炭素数6〜30のアリール基又は
炭素数3〜30のシクロアルキル基を示し、R3 ,R4
及びR 5 はそれぞれ水素,炭素数3〜30のアルキル
基,炭素数6〜30のアリール基又は炭素数3〜30の
シクロアルキル基を示し、R6 ,R7 及びR8 はそれぞ
れ炭素数2〜4のアルキレン基を示し、p,q及びrは
それぞれ0〜20を示し、R9 ,R10,R12及びR13
それぞれ水素,炭素数3〜30のアルキル基,炭素数6
〜30のアリール基又は炭素数3〜30のシクロアルキ
ル基を示し、R11は炭素数2〜4のアルキレン基を示
し、xは1〜20を示す。〕で表されるリン系化合物の
少なくとも一種及び(C)一般式(IV)
[Wherein R1And R2Each has 3 carbons
To 30 alkyl groups, C6 to C30 aryl groups, or
Represents a cycloalkyl group having 3 to 30 carbon atoms, R3, RFour
And R FiveAre hydrogen and alkyl having 3 to 30 carbon atoms, respectively.
Group, an aryl group having 6 to 30 carbon atoms or an aryl group having 3 to 30 carbon atoms
R represents a cycloalkyl group6, R7And R8Is that
Represents an alkylene group having 2 to 4 carbon atoms, p, q and r are
R is 0 to 20 respectively9, RTen, R12And R13Is
Hydrogen, an alkyl group having 3 to 30 carbon atoms, and 6 carbon atoms, respectively
To 30 aryl groups or C3 to C30 cycloalkyls
R group11Represents an alkylene group having 2 to 4 carbon atoms
However, x shows 1-20. ] Of the phosphorus compound represented by
At least one and (C) general formula (IV)

【0009】[0009]

【化8】 [Chemical 8]

【0010】〔式中、R14,R15及びR16は水素,炭素
数3〜30のアルキル基,炭素数6〜30のアリール基
又は炭素数3〜30のシクロアルキル基を示す。但し、
14,R15及びR16の少なくとも一つは水素以外の基で
あり、また1分子中の合計炭素数が6以上である。〕で
表されるアミン化合物とからなることを特徴とする潤滑
油組成物を提供するものである。
[In the formula, R 14 , R 15 and R 16 represent hydrogen, an alkyl group having 3 to 30 carbon atoms, an aryl group having 6 to 30 carbon atoms or a cycloalkyl group having 3 to 30 carbon atoms. However,
At least one of R 14 , R 15 and R 16 is a group other than hydrogen, and the total number of carbon atoms in one molecule is 6 or more. ] The present invention provides a lubricating oil composition comprising an amine compound represented by

【0011】先ず、本発明において、基油(A)の主成
分であるエステル系化合物は、一価又は多価脂肪酸エス
テルである。そして、その動粘度については特に制限は
ないが、通常は1〜500cSt (40℃)、好ましくは
10〜100cSt (40℃)である。動粘度が1cSt
(40℃)未満では、潤滑性不足となり、異常摩耗や焼
付を起こし好ましくない。また、500cSt (40℃)
を超えると、低温時油戻りが悪くなって、給油不足とな
り焼付を起こし好ましくない。これらの特性を有する具
体例としては、トリメチロールプロパントリ2−エチル
ヘキサノエート,ペンタエリスリトールテトラ2−エチ
ルヘキサノエート,ジオクチルアジペート等を挙げるこ
とができる。
First, in the present invention, the ester compound as the main component of the base oil (A) is a monovalent or polyvalent fatty acid ester. The kinematic viscosity is not particularly limited, but is usually 1 to 500 cSt (40 ° C), preferably 10 to 100 cSt (40 ° C). Kinematic viscosity is 1 cSt
If the temperature is lower than (40 ° C.), the lubricity becomes insufficient and abnormal wear or seizure occurs, which is not preferable. Also, 500cSt (40 ℃)
If it exceeds, the oil return at a low temperature becomes worse, and the oil supply becomes insufficient, causing seizure, which is not preferable. Specific examples having these characteristics include trimethylolpropane tri-2-ethylhexanoate, pentaerythritol tetra-2-ethylhexanoate, dioctyl adipate and the like.

【0012】次に、エステル系化合物を主成分とする基
油(A)に配合されるリン系化合物(B)としては、前
述した一般式(I),(II)あるいは(III)で表される
ものがあげられる。これらのリン系化合物は、一種又は
二種以上を混合して配合される。この(B)成分である
リン系化合物の配合割合は特に制限はなく、状況に応じ
て適宜選定すればよいが、通常はエステル系化合物を主
成分とする基油(A)に対して、0.001〜10重量%
で、好ましくは、0.01〜2重量%である。配合量が0.
001重量%未満では、摩耗防止効果が充分でなく好ま
しくない。また、10重量%を超えると摩耗防止効果が
飽和点に達して配合量に見合った効果を得ることができ
ず好ましくない。
Next, the phosphorus compound (B) blended with the base oil (A) containing an ester compound as a main component is represented by the above-mentioned general formula (I), (II) or (III). I can give you things. These phosphorus compounds are mixed alone or in combination of two or more. The blending ratio of the phosphorus compound as the component (B) is not particularly limited and may be appropriately selected depending on the situation, but is usually 0 with respect to the base oil (A) containing the ester compound as a main component. 0.001 to 10% by weight
And preferably 0.01 to 2% by weight. Compounding amount is 0.
If it is less than 001% by weight, the effect of preventing wear is not sufficient, which is not preferable. On the other hand, if it exceeds 10% by weight, the wear preventing effect reaches the saturation point and the effect corresponding to the blending amount cannot be obtained, which is not preferable.

【0013】上記一般式(I),(II)および(III)に
おいて、各記号は前述した通りである。すなわち、R1
及びR2 はそれぞれ炭素数3〜30のアルキル基、好ま
しくは炭素数6〜20のアルキル基(例えばヘキシル
基,オクチル基,デシル基,ラウリル基,ステアリル
基,オレイル基等),炭素数6〜30のアリール基、好
ましくは炭素数6〜20のアリール基(例えばフェニル
基,トリル基,キシリル基,ノニルフェニル基,ドデシ
ルフェニル基等)又は炭素数3〜30のシクロアルキル
基、好ましくは炭素数5〜15のシクロアルキル基(例
えばシクロペンチル基,シクロヘキシル基,トリメチル
シクロヘキシル基等)を示し、R3 ,R4 ,R5
9 ,R10,R12及びR13はそれぞれ水素,炭素数3〜
30のアルキル基、好ましくは炭素数6〜20のアルキ
ル基(例えばヘキシル基,オクチル基,デシル基,ラウ
リル基,ステアリル基,オレイル基等),炭素数6〜3
0のアリール基、好ましくは炭素数6〜20のアリール
基(例えばフェニル基,トリル基,キシリル基,ノニル
フェニル基等)又は炭素数3〜30のシクロアルキル
基、好ましくは炭素数5〜15のシクロアルキル基(例
えばシクロペンチル基,シクロヘキシル基,トリメチル
シクロペンチル基等)を示す。また、R6 ,R7,R8
及びR11はそれぞれ炭素数2〜4のアルキレン基(例え
ばエチレン,プロピレン基,ブチレン基)を示す。なお
p,q及びrはそれぞれ0〜20(整数に限らず、実数
を含む)、好ましくは2〜10を示し、またxは1〜2
0(整数に限らず、実数を含む)、好ましくは1〜10
を示す。この一般式(I)で表されるリン系化合物の具
体例としては、ジラウリルハイドロゲンホスファイト,
ジオレイルハイドロゲンホスファイト,ジフェニルハイ
ドロゲンホスファイトなどがあり、また一般式(II)で
表されるリン系化合物の具体例としては、トリス・ポリ
オキシエチレンデシルエーテルホスフェート,ジポリオ
キシエチレンノニルフェニルエーテルホスフェートなど
があり、一般式(III)で表されるリン系化合物の具体例
としては、テトラフェニルジプロピレングリコールジホ
スファイト,テトラトリデシルジエチレングリコールジ
ホスファイト等を挙げることができる。
In the above general formulas (I), (II) and (III), each symbol is as described above. That is, R 1
And R 2 are each an alkyl group having 3 to 30 carbon atoms, preferably an alkyl group having 6 to 20 carbon atoms (eg, hexyl group, octyl group, decyl group, lauryl group, stearyl group, oleyl group), 6 carbon atoms 30 aryl group, preferably 6 to 20 carbon aryl group (eg phenyl group, tolyl group, xylyl group, nonylphenyl group, dodecylphenyl group, etc.) or 3 to 30 carbon atom cycloalkyl group, preferably carbon number 5 to 15 cycloalkyl groups (for example, cyclopentyl group, cyclohexyl group, trimethylcyclohexyl group, etc.), R 3 , R 4 , R 5 ,
R 9 , R 10 , R 12 and R 13 are each hydrogen and 3 to 3 carbon atoms.
30 alkyl groups, preferably alkyl groups having 6 to 20 carbon atoms (for example, hexyl group, octyl group, decyl group, lauryl group, stearyl group, oleyl group), 6 to 3 carbon atoms
0 aryl group, preferably an aryl group having 6 to 20 carbon atoms (eg, phenyl group, tolyl group, xylyl group, nonylphenyl group, etc.) or a cycloalkyl group having 3 to 30 carbon atoms, preferably 5 to 15 carbon atoms A cycloalkyl group (eg, cyclopentyl group, cyclohexyl group, trimethylcyclopentyl group, etc.) is shown. In addition, R 6 , R 7 , and R 8
And R 11 each represent an alkylene group having 2 to 4 carbon atoms (for example, ethylene, propylene group, butylene group). Note that p, q, and r are each 0 to 20 (not limited to an integer, including a real number), preferably 2 to 10, and x is 1 to 2.
0 (not limited to integers, including real numbers), preferably 1 to 10
Indicates. Specific examples of the phosphorus compound represented by the general formula (I) include dilauryl hydrogen phosphite,
There are dioleyl hydrogen phosphite, diphenyl hydrogen phosphite, and the like. Specific examples of the phosphorus-based compound represented by the general formula (II) include tris-polyoxyethylene decyl ether phosphate and dipolyoxyethylene nonyl phenyl ether phosphate. And the like. Specific examples of the phosphorus compound represented by the general formula (III) include tetraphenyldipropylene glycol diphosphite and tetratridecyl diethylene glycol diphosphite.

【0014】また、エステル系化合物を主成分とする基
油(A)に配合されるアミン化合物(C)は、上記一般
式(IV)で表されるものである。ここで、R14,R15
びR 16はそれぞれ水素,炭素数3〜30のアルキル基,
炭素数6〜30のアリール基又は炭素数3〜30のシク
ロアルキル基、好ましくは炭素数6〜24のアルキル
基,アリール基,シクロアルキル基である。ただし、R
14,R15及びR16の少なくとも一つは水素以外の基であ
り、また1分子中の合計炭素数が6以上であることが必
要である。ここで、アルキル基は、直鎖,分岐,飽和あ
るいは不飽和のいずれでもよい。しかし、基油への溶解
安定性から、分岐又は不飽和アルキル基が好ましい。こ
のアミン化合物(C)の配合量については、特に制限は
ないが、通常はエステル系化合物を主成分とする基油
(A)に対して、0.001〜10重量%で、好ましく
は、0.01〜2重量%である。配合量が、0.001重量
%未満では、加水分解防止効果が不充分であり好ましく
ない。また、10重量%を超えると加水分解防止効果が
飽和点に達して配合量に見合った効果を得ることができ
ない。その上、摩耗防止や熱安定性に悪影響を及ぼすの
で好ましくない。このようなアミン化合物(C)の具体
例をあげれば、トリ(2−エチルヘキシル) アミン, ジ
(2−エチルヘキシル) アミン,tert−ドデシルアミ
ン,tert−オクタデシルアミン,tert−ベヘニルアミ
ン,オレイルアミン,ジオレイルアミン,イソステアリ
ルアミン,ジメチルオレイルアミン,ドデシルアニリ
ン,ジベンジルアミン,シクロヘキシルアミン,2−メ
チルシクロヘキシルアミン,シクロヘキシルドデシルア
ミン等を挙げることができる。
A group containing an ester compound as a main component
The amine compound (C) blended in the oil (A) is the above-mentioned general compound.
It is represented by formula (IV). Where R14, R15Over
And R 16Are hydrogen, an alkyl group having 3 to 30 carbon atoms,
Aryl group having 6 to 30 carbon atoms or siku having 3 to 30 carbon atoms
Alkyl group, preferably alkyl having 6 to 24 carbon atoms
A group, an aryl group, and a cycloalkyl group. However, R
14, R15And R16At least one of the groups is a group other than hydrogen.
And the total number of carbon atoms in one molecule must be 6 or more.
It is important. Here, the alkyl group has a straight chain, a branched chain, or a saturated chain.
It may be either saturated or unsaturated. However, dissolution in base oil
A branched or unsaturated alkyl group is preferred for stability. This
There is no particular limitation on the amount of the amine compound (C) compounded.
No, but usually a base oil mainly composed of ester compounds
It is preferably 0.001 to 10% by weight with respect to (A).
Is 0.01 to 2% by weight. Compounding amount is 0.001 weight
If it is less than%, the hydrolysis preventing effect is insufficient, which is preferable.
Absent. Further, if it exceeds 10% by weight, the effect of preventing hydrolysis is obtained.
The saturation point is reached, and the effect is
Absent. Moreover, it has a negative effect on wear prevention and thermal stability.
Is not preferable. Specific examples of such an amine compound (C)
For example, tri (2-ethylhexyl) amine, di
(2-Ethylhexyl) amine, tert-dodecylami
Amine, tert-octadecylamine, tert-behenylamine
, Oleylamine, dioleylamine, isostearia
Luamine, dimethyl oleylamine, dodecyl anili
Amine, dibenzylamine, cyclohexylamine, 2-me
Cylcyclohexylamine, cyclohexyldodecylure
Min, etc. can be mentioned.

【0015】なお、本発明の潤滑油組成物は、各種冷媒
(フロン系冷媒,代替フロン系冷媒等)を用いる冷凍機
油や油圧装置の作動油としても使用できることは勿論で
ある。そして、必要に応じて酸化防止剤,油性剤,銅不
活性剤,消泡剤等を任意に配合することもできる。
Of course, the lubricating oil composition of the present invention can also be used as a refrigerating machine oil using various refrigerants (CFC refrigerant, alternative CFC refrigerant, etc.) and hydraulic oil for hydraulic devices. Then, if necessary, an antioxidant, an oiliness agent, a copper deactivator, a defoaming agent and the like can be optionally mixed.

【0016】[0016]

【実施例】更に、本発明を実施例及び比較例により更に
詳しく説明する。 実施例1〜6及び比較例1〜8 第1表に示す基油を用い、これを第2表に示す配合比で
各成分を配合して潤滑油組成物を得、この組成物を試料
油として、下記の試験に供した。摩耗試験は、次の条件
でファレックス試験機により、ピンの摩耗量で評価し
た。また、加水分解試験は、次の条件でASTM D−
2619−88の加水分解試験法に準拠し、試験後の油
層の全酸価を測定した。更に、下記の条件でシールドチ
ューブ試験を行った。 摩耗試験条件 フロン134aの吹込み 10リットル/時間 荷重 300LBS, 時間 60分 テストピース材質 ピン SAE3135(AST
M D 2670−81標準材) ブロック AISI 1137(ASTM D 267
0−81標準材) 空気雰囲気下 荷重 300LBS, 時間 60分 テストピース材質 ピン SAE3135(AST
M D 2670−81標準材) ブロック AISI 1137(ASTM D 267
0−81標準材) 加水分解試験条件 温度 93℃, 時間 240時間 触媒 銅片(13×51×1mm) 油 75g , 水 25g シールドチューブ試験条件 温度 175℃, 時間 720時間, 冷媒 フロ
ン134a
The present invention will be described in more detail with reference to Examples and Comparative Examples. Examples 1 to 6 and Comparative Examples 1 to 8 The base oils shown in Table 1 were used, and the components were blended at the blending ratios shown in Table 2 to obtain lubricating oil compositions, and the compositions were used as sample oils. As a result, the following test was performed. The wear test evaluated the wear amount of the pin by the Falex tester under the following conditions. Further, the hydrolysis test was conducted under the following conditions according to ASTM D-
According to the hydrolysis test method of 2619-88, the total acid value of the oil layer after the test was measured. Further, a shield tube test was conducted under the following conditions. Abrasion test conditions Blowing of Freon 134a 10 liters / hour load 300 LBS, time 60 minutes Test piece material pin SAE3135 (AST
MD 2670-81 standard material) Block AISI 1137 (ASTM D 267
0-81 standard material) Load under air atmosphere 300LBS, time 60 minutes Test piece material pin SAE3135 (AST
MD 2670-81 standard material) Block AISI 1137 (ASTM D 267
0-81 standard material) Hydrolysis test condition temperature 93 ℃, time 240 hours Catalyst copper piece (13 x 51 x 1 mm) Oil 75g, water 25g Shield tube test condition temperature 175 ℃, time 720 hours, refrigerant Freon 134a

【0017】[0017]

【表1】 [Table 1]

【0018】[0018]

【表2】 [Table 2]

【0019】さらに、実施した各試験項目の結果を第3
表に示す。
Furthermore, the result of each test item carried out is shown in the third
Shown in the table.

【0020】[0020]

【表3】 [Table 3]

【0021】第3表の試験結果から判るように、本発明
によるとシ−ルドチューブ試験は全く問題なく良好で、
しかも摩耗量が少なく、かつ加水分解後の全酸価の上昇
もなく優れていることが判る。一方、比較例では、シ−
ルドチューブ試験は全く問題なく良好ではあるが、いず
れも耐摩耗性、耐加水分解性のどちらかの特性に欠けて
いることが判る。
As can be seen from the test results in Table 3, according to the present invention, the shield tube test is satisfactory without any problems.
Moreover, it is understood that the amount of wear is small and the total acid value after hydrolysis is not increased, which is excellent. On the other hand, in the comparative example,
Although the cold tube test was satisfactory without any problems, it was found that both of them lacked the wear resistance and the hydrolysis resistance.

【発明の効果】【The invention's effect】

【0022】叙上の如く、本発明によれば、シ−ルドチ
ューブ試験は全く問題なく良好で、かつフロン雰囲気下
での耐摩耗性、耐加水分解性も極めて優れており、冷凍
機の潤滑油として使用したときに発揮される効果は、十
分に期待でき、その使用効果は極めて大なるものがあ
る。更に、本発明の潤滑油組成物は、空気雰囲気下でも
耐摩耗性に優れ、耐加水分解性も極めて優れており、油
圧作動油等その他の潤滑油としても、その作用効果は極
めて大きい。
As described above, according to the present invention, the shield tube test is satisfactory without any problem, and the abrasion resistance and the hydrolysis resistance under the fluorocarbon atmosphere are also very excellent, and the refrigerator lubrication is excellent. The effect exhibited when used as oil can be expected sufficiently, and the effect of use can be extremely large. Further, the lubricating oil composition of the present invention has excellent wear resistance even in an air atmosphere and extremely excellent hydrolysis resistance, and its action and effect are extremely large even when used as other lubricating oil such as hydraulic oil.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 C10M 137:02) C10N 30:06 40:30 ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 5 Identification code Office reference number FI technical display location C10M 137: 02) C10N 30:06 40:30

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 (A)エステル系化合物を主成分とする
基油,(B)一般式(I),(II)あるいは(III) 【化1】 【化2】 【化3】 〔式中、R1 及びR2 はそれぞれ炭素数3〜30のアル
キル基,炭素数6〜30のアリール基又は炭素数3〜3
0のシクロアルキル基を示し、R3 ,R4 及びR 5 はそ
れぞれ水素,炭素数3〜30のアルキル基,炭素数6〜
30のアリール基又は炭素数3〜30のシクロアルキル
基を示し、R6 ,R7 及びR8 はそれぞれ炭素数2〜4
のアルキレン基を示し、p,q及びrはそれぞれ0〜2
0を示し、R9 ,R10,R12及びR13はそれぞれ水素,
炭素数3〜30のアルキル基,炭素数6〜30のアリー
ル基又は炭素数3〜30のシクロアルキル基を示し、R
11は炭素数2〜4のアルキレン基を示し、xは1〜20
を示す。〕で表されるリン系化合物の少なくとも一種及
び(C)一般式(IV) 【化4】 〔式中、R14,R15及びR16は水素,炭素数3〜30の
アルキル基,炭素数6〜30のアリール基又は炭素数3
〜30のシクロアルキル基を示す。但し、R14,R15
びR16の少なくとも一つは水素以外の基であり、また1
分子中の合計炭素数が6以上である。〕で表されるアミ
ン化合物とからなることを特徴とする潤滑油組成物。
1. A main component of (A) an ester compound
Base oil, (B) General formula (I), (II) or (III) [Chemical 1] [Chemical 2] [Chemical 3] [In the formula, R1And R2Is an alkane having 3 to 30 carbon atoms
Kill group, aryl group having 6 to 30 carbon atoms or 3 to 3 carbon atoms
Represents a cycloalkyl group of 0, R3, RFourAnd R FiveHaso
Hydrogen, an alkyl group having 3 to 30 carbon atoms, and 6 to 6 carbon atoms, respectively
30 aryl groups or cycloalkyl having 3 to 30 carbon atoms
Group, R6, R7And R8Has 2 to 4 carbon atoms
Is an alkylene group, and p, q and r are each 0 to 2
0, R9, RTen, R12And R13Are hydrogen,
C3-C30 alkyl group, C6-C30 aryl
Group or a cycloalkyl group having 3 to 30 carbon atoms, R
11Represents an alkylene group having 2 to 4 carbon atoms, and x is 1 to 20.
Indicates. ] At least one phosphorus compound represented by
(C) General formula (IV) [Chemical 4] [In the formula, R14, R15And R16Is hydrogen, having 3 to 30 carbon atoms
Alkyl group, aryl group having 6 to 30 carbon atoms or 3 carbon atoms
~ 30 cycloalkyl groups are shown. However, R14, R15Over
And R16At least one of the groups is a group other than hydrogen, and 1
The total number of carbon atoms in the molecule is 6 or more. ] Ami
A lubricating oil composition.
【請求項2】 請求項1記載の潤滑油組成物からなるこ
とを特徴とする冷凍機油。
2. A refrigerating machine oil comprising the lubricating oil composition according to claim 1.
JP3176555A 1991-07-17 1991-07-17 Lubricating oil composition Expired - Fee Related JP2966975B2 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
JP3176555A JP2966975B2 (en) 1991-07-17 1991-07-17 Lubricating oil composition
EP92111780A EP0523561A1 (en) 1991-07-17 1992-07-10 Lubricating oil composition
KR1019920012862A KR930002490A (en) 1991-07-17 1992-07-18 Lubricant composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3176555A JP2966975B2 (en) 1991-07-17 1991-07-17 Lubricating oil composition

Publications (2)

Publication Number Publication Date
JPH0517794A true JPH0517794A (en) 1993-01-26
JP2966975B2 JP2966975B2 (en) 1999-10-25

Family

ID=16015632

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (3)

Country Link
EP (1) EP0523561A1 (en)
JP (1) JP2966975B2 (en)
KR (1) KR930002490A (en)

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JPH07179875A (en) * 1993-12-24 1995-07-18 Tonen Corp Lubricating oil composition for drive hydraulic system
JP2000239688A (en) * 1999-02-17 2000-09-05 Sanyo Chem Ind Ltd Abrasion resistance improver
WO2002008366A1 (en) 2000-07-26 2002-01-31 Idemitsu Kosan Co., Ltd. Lubricating oil for refrigerator and hydraulic fluid composition for refrigerator using the same
JP2009078339A (en) * 2007-09-27 2009-04-16 Tipton Mfg Corp Media for dry barrel polishing and dry barrel polishing method
WO2010064347A1 (en) * 2008-12-01 2010-06-10 新日本石油株式会社 Flame retardant hydraulic oil composition
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US5968880A (en) * 1997-10-23 1999-10-19 The Lubrizol Corporation Lubricating compositions, functional fluids and greases containing thiophosphorus esters or their salts with a oxyalkylene group, and methods of using the same
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Publication number Priority date Publication date Assignee Title
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JPH07179875A (en) * 1993-12-24 1995-07-18 Tonen Corp Lubricating oil composition for drive hydraulic system
JP2000239688A (en) * 1999-02-17 2000-09-05 Sanyo Chem Ind Ltd Abrasion resistance improver
WO2002008366A1 (en) 2000-07-26 2002-01-31 Idemitsu Kosan Co., Ltd. Lubricating oil for refrigerator and hydraulic fluid composition for refrigerator using the same
JP2009078339A (en) * 2007-09-27 2009-04-16 Tipton Mfg Corp Media for dry barrel polishing and dry barrel polishing method
WO2010064347A1 (en) * 2008-12-01 2010-06-10 新日本石油株式会社 Flame retardant hydraulic oil composition
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US11485926B2 (en) 2019-01-23 2022-11-01 Eneos Corporation Refrigerant oil and method for producing refrigerant oil

Also Published As

Publication number Publication date
KR930002490A (en) 1993-02-23
EP0523561A1 (en) 1993-01-20
JP2966975B2 (en) 1999-10-25

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