JPH08143890A - Lubricant composition for rolling - Google Patents

Lubricant composition for rolling

Info

Publication number
JPH08143890A
JPH08143890A JP6311169A JP31116994A JPH08143890A JP H08143890 A JPH08143890 A JP H08143890A JP 6311169 A JP6311169 A JP 6311169A JP 31116994 A JP31116994 A JP 31116994A JP H08143890 A JPH08143890 A JP H08143890A
Authority
JP
Japan
Prior art keywords
group
branched
rolling
mass
carbon atoms
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
JP6311169A
Other languages
Japanese (ja)
Other versions
JP3406407B2 (en
Inventor
Shigetoshi Ogura
茂稔 小倉
Katsumi Seki
克己 関
Hideo Yokota
秀雄 横田
Junichi Shibata
潤一 柴田
Yoshitaka Natsume
芳孝 夏目
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.)
Eneos Corp
Original Assignee
Nippon Oil Corp
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 Nippon Oil Corp filed Critical Nippon Oil Corp
Priority to JP31116994A priority Critical patent/JP3406407B2/en
Priority to EP95850199A priority patent/EP0712925A3/en
Priority to TW084112004A priority patent/TW294716B/zh
Priority to KR1019950042207A priority patent/KR100423478B1/en
Publication of JPH08143890A publication Critical patent/JPH08143890A/en
Application granted granted Critical
Publication of JP3406407B2 publication Critical patent/JP3406407B2/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
    • C10M173/00Lubricating compositions containing more than 10% water
    • C10M173/02Lubricating compositions containing more than 10% water not containing mineral or fatty oils
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    • C10M129/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
    • C10M129/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
    • C10M129/04Hydroxy compounds
    • C10M129/06Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M129/08Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms containing at least 2 hydroxy groups
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    • C10M129/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
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    • C10M129/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
    • C10M129/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
    • C10M129/26Carboxylic acids; Salts thereof
    • C10M129/28Carboxylic acids; Salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M129/38Carboxylic acids; Salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having 8 or more carbon atoms
    • C10M129/40Carboxylic acids; Salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having 8 or more carbon atoms monocarboxylic
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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
    • C10M133/08Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups
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    • C10M145/00Lubricating compositions characterised by the additive being a macromolecular compound containing oxygen
    • C10M145/18Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M145/24Polyethers
    • C10M145/26Polyoxyalkylenes
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    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
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    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/125Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
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    • C10M2209/103Polyethers, i.e. containing di- or higher polyoxyalkylene groups
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    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/20Metal working
    • C10N2040/24Metal working without essential removal of material, e.g. forming, gorging, drawing, pressing, stamping, rolling or extruding; Punching metal
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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Lubricants (AREA)
  • Paper (AREA)

Abstract

PURPOSE: To obtain a lubricant composition containing water, a specific oxygen- containing compound, a fatty acid salt, having firepreventing property, cooling property, rolling property and gloss property on metal surface after rolling, excellent in storage stability, not producing oil stain and capable of filtering and removing abrasive powder in rolling. CONSTITUTION: This composition contains (A) 5-89.95wt.% of water, (B) 10-94.95wt.% of an oxygen-containing compound of the formula R<1> O-(R<3> -O)p -R<2> [R<1> and R<2> are H or a 1-18C hydrocarbon group; R<3> is a 1-6C alkylene; (p) is 1-30] and (C) 0.05-10wt.% of at least one kind of a fatty acid salt selected from a group of a 6-22C fatty acid alkali metal salt, a salt of a 6-22C fatty acid and a 1-15C alkanolamine and a salt of a 6-22C fatty acid and a compound of the formula R<4> is a 1-24C hydrocarbon group; R<5> is ethylene group or propylene group; X is H, R<4> or a group of the formula (R<6> -O)rH [R<6> is R<5> ; (r) is 1-30]; (q) is (r)} and has 80-99.95wt.% of total content of the components A and B.

Description

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

【0001】[0001]

【産業上の利用分野】本発明は圧延用潤滑剤組成物に関
するものであって、さらに詳しくは、ステンレス鋼、
銅、アルミニウム及びそれらの合金などの如く、表面光
沢が良好であることが要求される金属材料を圧延加工す
る際の潤滑剤として特に好適な圧延用潤滑剤組成物に係
る。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a lubricant composition for rolling, more specifically, stainless steel,
The present invention relates to a lubricant composition for rolling, which is particularly suitable as a lubricant for rolling metal materials such as copper, aluminum and alloys thereof, which are required to have good surface gloss.

【0002】[0002]

【従来の技術】金属材料を圧延機で圧延して薄い金属板
に加工する技術としては、熱間圧延と冷間圧延が知られ
ている。冷間圧延を行うに際しては、押し並べて潤滑油
を使用するのが通例であり、熱間圧延でもアルミニウム
やアルミニウム合金を圧延する場合には潤滑油が一般に
使用される。そして、これらの場合の潤滑油としては、
低粘度の鉱油やエステルなどの合成油に、各種の添加剤
を配合した圧延油が、古くは使用されていた。しかし、
この種の圧延油は引火性が高いため、高速圧延時に火災
を起こす危険があった。こうした事情から近年では、非
可燃性で冷却性に優れるという水の性質を利用して、低
粘度鉱油、エステルなどの合成油またはパーム油、牛油
などの油脂類を乳化剤の存在下に水に乳化させた、所謂
エマルション型圧延油が多用されている。しかしなが
ら、これらのエマルション型圧延油は、乳化安定性に乏
しい、不均一系であるため、圧延加工後の金属板の表面
に光沢ぬらが生じ易い、圧延性が乏しい、圧延加工に際
して発生した摩耗粉やスカム(摩耗粉と油分とが凝集し
たもの)を濾過分離する際に、系内の圧延油のロスを伴
うなどの欠点がある。また、特開昭60−118790
号公報には、(イ)カルボン酸、スルフォン酸、ナフテ
ン酸などの酸の塩またはアミドと、(ロ)アルキレング
リコールと、(ハ)鉱油、合成油または油脂と、(ニ)
水とからなる組成物中に水を可溶化した、所謂、水可溶
化型の金属加工油が開示されている。この金属加工油は
難燃性ではあるものの、冷却性が充分でなく、可溶化さ
せる水の量によって粘度が大きく変化してしまう点で問
題があった。
2. Description of the Related Art Hot rolling and cold rolling are known as techniques for rolling a metal material into a thin metal plate by rolling it with a rolling mill. When performing cold rolling, it is customary to use a lubricating oil by pressing them side by side, and even in the case of hot rolling, lubricating oil is generally used when rolling aluminum or aluminum alloy. And as the lubricating oil in these cases,
Rolling oils prepared by mixing various additives with synthetic oils such as low-viscosity mineral oils and esters have been used for a long time. But,
Since this type of rolling oil is highly flammable, there was a risk of causing a fire during high speed rolling. Under these circumstances, in recent years, by utilizing the property of water that is non-flammable and has excellent cooling properties, low-viscosity mineral oil, synthetic oil such as ester, or oils and fats such as palm oil and beef oil are converted into water in the presence of an emulsifier. A so-called emulsion type rolling oil that has been emulsified is often used. However, since these emulsion type rolling oils are poor in emulsion stability and are a heterogeneous system, gloss wetness is likely to occur on the surface of the metal plate after rolling, rolling is poor, and abrasion powder generated during rolling is generated. There is a drawback such as the loss of rolling oil in the system when filtering and separating scum (scattering abrasion powder and oil). In addition, JP-A-60-118790
(A) carboxylic acid, sulfonic acid, naphthenic acid and other acid salts or amides, (b) alkylene glycol, (c) mineral oil, synthetic oil or fat, and (d)
A so-called water-solubilizing metal working oil in which water is solubilized in a composition consisting of water is disclosed. Although this metalworking oil is flame-retardant, it has a problem in that it does not have sufficient cooling properties and its viscosity greatly changes depending on the amount of solubilized water.

【0003】[0003]

【発明が解決しようとする課題】本発明者らは従来の圧
延油に指摘される様々な欠点を克服すべく研究を重ねた
結果、特定な含酸素化合物と特定な脂肪酸塩と水を必須
成分とし、これら3成分の含有量が所定の範囲にある組
成物が、圧延用潤滑油としての各種の性能に優れている
ことを見い出した。本発明の目的は、火災防火性、冷却
性、圧延性、圧延後の金属板表面の光沢性が良好であっ
て、貯蔵安定性にも優れ、オイルステインが発生せず、
しかも圧延加工に際して生じた摩耗粉の濾過除去が可能
な圧延用潤滑剤組成物を提供することにある。
DISCLOSURE OF THE INVENTION As a result of repeated studies to overcome various drawbacks pointed out in conventional rolling oils, the present inventors have found that a specific oxygen-containing compound, a specific fatty acid salt and water are essential components. It was found that a composition containing these three components in a predetermined range is excellent in various properties as a lubricating oil for rolling. The object of the present invention is fire fireproofing, cooling, rollability, good gloss of the metal plate surface after rolling, excellent storage stability, no oil stain occurs,
Moreover, it is an object of the present invention to provide a rolling lubricant composition capable of removing abrasion powder generated during rolling by filtration.

【0004】[0004]

【課題を解決するための手段】本発明に係る圧延用潤滑
剤組成物は、組成物全量基準で、 (A)水 5〜89.95質量%、 (B)下記の(1)式で表される含酸素化合物 10〜94.95質量%、 R1 O−(R3 −O)p −R2 (1) [ここで、R1 およびR2 はそれぞれ個別に水素または炭素数1〜18の炭 化水素基を示し、R3 は炭素数1〜6のアルキレン基を示し、pは1〜 30の数を示す。] (C)下記の(a)〜(c)から選ばれる少なくとも1種の脂肪酸塩 0.05〜10質量%、 (a)炭素数6〜22の脂肪酸のアルカリ金属塩 (b)炭素数6〜22の脂肪酸と、炭素数1〜15のアルカノールアミン との塩 (c)炭素数6〜22の脂肪酸と、下記の(2)式で表される含窒素化合 物との塩 [ここで、R4 は炭素数1〜24の炭化水素基を示し、
5 はエチレン基又はプロピレン基を示し、qは1〜3
0の数を示し、Xは水素、炭素数1〜24の炭化水素基
又は一般式−(R6 −O)r Hで示される基を示し、R
6 はエチレン基又はプロピレン基を示し、rは1〜30
の数を示す。]を含有し、上記(1)式で表した含酸素
化合物および水の合計含有量が、組成物全量基準で80
〜99.95質量%であることを特徴とする。
The lubricant composition for rolling according to the present invention is represented by (A) water 5 to 89.95% by mass, and (B) the following formula (1) on the basis of the total amount of the composition. Oxygen-containing compound 10 to 94.95% by mass, R 1 O— (R 3 —O) p —R 2 (1) [wherein R 1 and R 2 are independently hydrogen or C 1 to C 18 R 3 represents an alkylene group having 1 to 6 carbon atoms, and p represents a number of 1 to 30. ] (C) At least one fatty acid salt selected from the following (a) to (c): 0.05 to 10% by mass, (a) Alkali metal salt of a fatty acid having 6 to 22 carbon atoms (b) 6 carbon atoms To a fatty acid having 22 to 22 carbon atoms and an alkanolamine having 1 to 15 carbon atoms (c) a salt having 6 to 22 carbon atoms and a nitrogen-containing compound represented by the following formula (2) [Here, R 4 represents a hydrocarbon group having 1 to 24 carbon atoms,
R 5 represents an ethylene group or a propylene group, and q is 1 to 3
Represents a number of 0, X represents hydrogen, a hydrocarbon group having 1 to 24 carbon atoms or a group represented by the general formula-(R 6 -O) r H, and R
6 represents an ethylene group or a propylene group, r is 1 to 30
Indicates the number of. ], The total content of the oxygen-containing compound represented by the above formula (1) and water is 80 based on the total amount of the composition.
It is characterized by being -99.95 mass%.

【0005】本発明に係る潤滑剤組成物の(A)成分で
ある水は、硬水であっても軟水であってもよく、従っ
て、これには水道水、工業用水、イオン交換水、蒸留水
などを任意に使用することができる。組成物における水
の含有量の下限は、組成物全量基準で5質量%、好まし
くは15質量%、より好ましくは25質量%であり、上
限は同じく組成物全量基準で89.95質量%、好まし
くは79.9質量%、より好ましくは69.8質量%で
ある。水の含有量が5質量%未満の場合は、潤滑剤組成
物の冷却性が低下し、圧延加工に際して焼き付きを起こ
し易く、89.95質量%を越える場合は、潤滑性が悪
化する。
The water as the component (A) of the lubricant composition according to the present invention may be hard water or soft water, and therefore, it may be tap water, industrial water, ion-exchanged water, distilled water. Etc. can be used arbitrarily. The lower limit of the water content in the composition is 5% by mass, preferably 15% by mass, more preferably 25% by mass, based on the total amount of the composition, and the upper limit is 89.95% by mass, also based on the total amount of the composition, preferably Is 79.9% by mass, more preferably 69.8% by mass. When the content of water is less than 5% by mass, the cooling property of the lubricant composition is lowered and seizure is likely to occur during rolling, and when it exceeds 89.95% by mass, the lubricity is deteriorated.

【0006】本発明に係る潤滑剤組成物の(B)成分
は、上記の(1)式で規定される。当該一般式における
1 およびR2 はそれぞれ水素または炭素数1〜18の
炭化水素基を示すが、R1 とR2 とは同一であっても、
異なっていても差し支えない。そして、炭素数1〜18
の炭化水素基としては、メチル基、エチル基、n−プロ
ピル基、イソプロピル基、n−ブチル基、イソブチル
基、sec−ブチル基、tert−ブチル基、直鎖また
は分枝のペンチル基、直鎖または分枝のヘキシル基、直
鎖または分枝のヘプチル基、直鎖または分枝のオクチル
基、直鎖または分枝のノニル基、直鎖または分枝のデシ
ル基、直鎖または分枝のウンデシル基、直鎖または分枝
のドデシル基、直鎖または分枝のトリデシル基、直鎖ま
たは分枝のテトラデシル基、直鎖または分枝のペンタデ
シル基、直鎖または分枝のヘキサデシル基、直鎖または
分枝のヘプタデシル基、直鎖または分枝のオクタデシル
基などの各アルキル基;直鎖または分枝のペンテニル
基、直鎖または分枝のオクテニル基、直鎖または分枝の
ヘキセニル基、直鎖または分枝のヘプテニル基、直鎖ま
たは分枝のオクテニル基、直鎖または分枝のノネニル
基、直鎖または分枝のデセニル基、直鎖または分枝のウ
ンデセニル基、直鎖または分枝のドデセニル基、直鎖ま
たは分枝のトリデセニル基、直鎖または分枝のテトラデ
セニル基、直鎖または分枝のペンタデセニル基、直鎖ま
たは分枝のヘキサデセニル基、直鎖または分枝のヘプタ
デセニル基、直鎖または分枝のオクタデセニル基などの
炭素数5〜18のアルケニル基;シクロペンチル基、シ
クロヘキシル基、シクロヘプチル基などの炭素数5〜7
のシクロアルキル基;メチルシクロペンチル基、ジメチ
ルシクロペンチル基(全ての置換異性体を含む)、メチ
ルエチルシクロペンチル基(全ての置換異性体を含
む)、ジエチルシクロペンチル基(全ての置換異性体を
含む)、メチルシクロヘキシル基、ジメチルシクロヘキ
シル基(全ての置換異性体を含む)、メチルエチルシク
ロヘキシル基(全ての置換異性体を含む)、ジエチルシ
クロヘキシル基(全ての置換異性体を含む)、メチルシ
クロヘプチル基、ジメチルシクロヘプチル基(全ての置
換異性体を含む)、メチルエチルシクロヘプチル基(全
ての置換異性体を含む)、ジエチルシクロヘプチル基
(全ての置換異性体を含む)などの炭素数6〜11のア
ルキルシクロアルキル基;フェニル基、ナフチル基など
のアリール基:トリル基、キシリル基(全ての置換異性
体を含む)、エチルフェニル基、直鎖または分枝のプロ
ピルフェニル基、直鎖または分枝のブチルフェニル基、
直鎖または分枝のペンチルフェニル基、直鎖または分枝
のヘキシルフェニル基、直鎖または分枝のヘプチルフェ
ニル基、直鎖または分枝のオクチルフェニル基、直鎖ま
たは分枝のノニルフェニル基、直鎖または分枝のデシル
フェニル基、直鎖または分枝のウンデシルフェニル基、
直鎖または分枝のドデシルフェニル基などの炭素数7〜
18の各アルキルアリール基;ベンシル基、フェニルエ
チル基、フェニルプロピル基(プロピル基の異性体を含
む)、フェニルブチル基(ブチル基の異性体を含む)、
フェニルペンチル基(ペンチル基の異性体を含む)、フ
ェニルヘキシル基(ヘキシル基の異性体を含む)などの
炭素数7〜12の各アリールアルキル基;などが包含さ
れる。(B)成分と(A)成分との相溶性を考慮する
と、(1)式におけるR1 およびR2 が個別に、水素、
炭素数1〜18のアルキル基、フェニル基または炭素数
7〜15のアルキルアリール基の何れかであることが好
ましい。
The component (B) of the lubricant composition according to the present invention is defined by the above formula (1). R 1 and R 2 in the general formula each represent hydrogen or a hydrocarbon group having 1 to 18 carbon atoms, but even if R 1 and R 2 are the same,
It does not matter if they are different. And, carbon number 1-18
As the hydrocarbon group of, a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, an isobutyl group, a sec-butyl group, a tert-butyl group, a linear or branched pentyl group, a linear chain Or a branched hexyl group, a straight-chain or branched heptyl group, a straight-chain or branched octyl group, a straight-chain or branched nonyl group, a straight-chain or branched decyl group, a straight-chain or branched undecyl group Group, straight-chain or branched dodecyl group, straight-chain or branched tridecyl group, straight-chain or branched tetradecyl group, straight-chain or branched pentadecyl group, straight-chain or branched hexadecyl group, straight-chain or Each alkyl group such as a branched heptadecyl group, a straight chain or branched octadecyl group; a straight chain or branched pentenyl group, a straight chain or branched octenyl group, a straight chain or branched hexenyl group, a straight chain Is a branched heptenyl group, a straight-chain or branched octenyl group, a straight-chain or branched nonenyl group, a straight-chain or branched decenyl group, a straight-chain or branched undecenyl group, a straight-chain or branched dodecenyl group. Group, straight-chain or branched tridecenyl group, straight-chain or branched tetradecenyl group, straight-chain or branched pentadecenyl group, straight-chain or branched hexadecenyl group, straight-chain or branched heptadecenyl group, straight-chain or C5-C18 alkenyl groups such as branched octadecenyl groups; C5-C7 cyclopentyl groups, cyclohexyl groups, cycloheptyl groups, etc.
Cycloalkyl group; methylcyclopentyl group, dimethylcyclopentyl group (including all substituted isomers), methylethylcyclopentyl group (including all substituted isomers), diethylcyclopentyl group (including all substituted isomers), methyl Cyclohexyl group, dimethylcyclohexyl group (including all substitution isomers), methylethylcyclohexyl group (including all substitution isomers), diethylcyclohexyl group (including all substitution isomers), methylcycloheptyl group, dimethylcyclo C6-C11 alkylcyclo such as heptyl group (including all substitution isomers), methylethylcycloheptyl group (including all substitution isomers), diethylcycloheptyl group (including all substitution isomers) Alkyl group; aryl group such as phenyl group and naphthyl group: tolyl group (Including all isomers) xylyl, ethylphenyl group, a linear or branched propylphenyl group, a linear or branched butylphenyl group,
A straight-chain or branched pentylphenyl group, a straight-chain or branched hexylphenyl group, a straight-chain or branched heptylphenyl group, a straight-chain or branched octylphenyl group, a straight-chain or branched nonylphenyl group, A straight chain or branched decylphenyl group, a straight chain or branched undecylphenyl group,
7 to 7 carbon atoms such as linear or branched dodecylphenyl group
18 alkylaryl groups; benzyl group, phenylethyl group, phenylpropyl group (including propyl group isomers), phenylbutyl group (including butyl group isomers),
Each arylalkyl group having 7 to 12 carbon atoms such as phenylpentyl group (including isomers of pentyl group), phenylhexyl group (including isomers of hexyl group), and the like are included. Considering the compatibility between the component (B) and the component (A), R 1 and R 2 in the formula (1) are independently hydrogen,
It is preferably either an alkyl group having 1 to 18 carbon atoms, a phenyl group or an alkylaryl group having 7 to 15 carbon atoms.

【0007】(1)式のR3 で示すアルキレン基には、
メチレン基のほか、メチルメチレン基(エチリデン
基)、エチレン基(以上炭素数2); エチルメチレン
基(プロピリデン基)、ジメチルメチレン基(イソプロ
ピリデン基)、メチルエチレン基(プロピレン基)、ト
リメチレン基(以上炭素数3);n−プロピルメチレン
基(ブチリデン基)、イソプロピルメチレン基(イソブ
チリデン基)、エチルメチルメチレン基、エチルエチレ
ン基、1,1−ジメチルエチレン基、1,2−ジメチル
エチレン基、1−メチルトリメチレン基、2−メチルト
リメチレン基、テトラメチレン基(以上炭素数4);n
−ブチルメチレン基(ペンチリデン基)、sec−ブチ
ルメチレン基、イソブチルメチレン基(イソペンチリデ
ン基)、tert−ブチルメチレン基、n−プロピルメ
チルメチレン基、イソプロピルメチルメチレン基、ジエ
チルメチレン基、n−プロピルエチレン基、イソプロピ
ルエチレン基、1−エチル−1−メチルエチレン基、1
−エチル−2−メチルエチレン基、トリメチルエチレン
基、1−エチルトリメチレン基、2−エチルトリメチレ
ン基、1,1−ジメチルトリメチレン基、1,2−ジメ
チルトリメチレン基、1,3−ジメチルトリメチレン
基、2,2−ジメチルトリメチレン基、1−メチルテト
ラメチレン基、2−メチルテトラメチレン基、ペンタメ
チレン基(以上炭素数5);n−ペンチルメチレン基
(ヘキシリデン基)、(1−メチルブチル基)メチレン
基、イソペンチルメチレン基(イソペンチリデン基)、
(1,2−ジメチルプロピル)メチレン基、n−ブチル
メチルメチレン基、イソブチルメチルメチレン基、エチ
ル−n−プロピルメチレン基、エチルイソプロピルメチ
レン基、ブチルエチレン基、イソブチルエチレン基、1
−(n−プロピル)−1−メチルエチレン基、1−(n
−プロピル)−2−メチルエチレン基、1−イソプロピ
ル−1−メチルエチレン基、1−イソプロピル−2−メ
チルエチレン基、1,2−ジエチルエチレン基、1−エ
チル−2,2−ジメチルエチレン基、テトラメチルエチ
レン基、1−n−プロピルトリメチレン基、2−n−プ
ロピルトリメチレン基、1−イソプロピルトリメチレン
基、2−イソプロピルトリメチレン基、1−エチル−3
−メチルトリメチレン基、1−エチル−2−メチルトリ
メチレン基、1,1,2−トリメチルトリメチレン基、
1,1,3−トリメチルトリメチレン基、1−エチルテ
トラメチレン基、1,1−ジメチルテトラメチレン基、
1,3−ジメチルテトラメチレン基、1,4−ジメチル
テトラメチレン基、2,2−ジメチルテトラメチレン
基、1−メチルペンタメチレン基、2−メチルペンタメ
チレン基、ヘキサメチレン基(以上炭素数6)などが包
含される。(B)成分と(A)成分との相溶性を考慮す
ると、(1)式におけるR3 は炭素数2〜6のアルキレ
ン基であることが好ましい。(1)式におけるpは1〜
30の数を示し、好ましくは1〜10の範囲にある。な
お、(1)式における−(R3 −O)p −はオキシアル
キレン基を示すが、pが2以上の場合は、単一構造のポ
リオキシアルキレン基を示すだけでなく、構造が異なる
2種以上のオキシアルキレン基が、ランダム共重合、交
互共重合またはブロック共重合したポリオキシアルキレ
ン基を示す。
In the alkylene group represented by R 3 in the formula (1),
In addition to methylene group, methylmethylene group (ethylidene group), ethylene group (having 2 or more carbon atoms); ethylmethylene group (propylidene group), dimethylmethylene group (isopropylidene group), methylethylene group (propylene group), trimethylene group ( C3 or more; n-propylmethylene group (butylidene group), isopropylmethylene group (isobutylidene group), ethylmethylmethylene group, ethylethylene group, 1,1-dimethylethylene group, 1,2-dimethylethylene group, 1 -Methyltrimethylene group, 2-methyltrimethylene group, tetramethylene group (above carbon number 4); n
-Butylmethylene group (pentylidene group), sec-butylmethylene group, isobutylmethylene group (isopentylidene group), tert-butylmethylene group, n-propylmethylmethylene group, isopropylmethylmethylene group, diethylmethylene group, n-propyl Ethylene group, isopropylethylene group, 1-ethyl-1-methylethylene group, 1
-Ethyl-2-methylethylene group, trimethylethylene group, 1-ethyltrimethylene group, 2-ethyltrimethylene group, 1,1-dimethyltrimethylene group, 1,2-dimethyltrimethylene group, 1,3-dimethyl Trimethylene group, 2,2-dimethyltrimethylene group, 1-methyltetramethylene group, 2-methyltetramethylene group, pentamethylene group (having 5 or more carbon atoms); n-pentylmethylene group (hexylidene group), (1- Methylbutyl group) methylene group, isopentylmethylene group (isopentylidene group),
(1,2-Dimethylpropyl) methylene group, n-butylmethylmethylene group, isobutylmethylmethylene group, ethyl-n-propylmethylene group, ethylisopropylmethylene group, butylethylene group, isobutylethylene group, 1
-(N-Propyl) -1-methylethylene group, 1- (n
-Propyl) -2-methylethylene group, 1-isopropyl-1-methylethylene group, 1-isopropyl-2-methylethylene group, 1,2-diethylethylene group, 1-ethyl-2,2-dimethylethylene group, Tetramethylethylene group, 1-n-propyltrimethylene group, 2-n-propyltrimethylene group, 1-isopropyltrimethylene group, 2-isopropyltrimethylene group, 1-ethyl-3
-Methyltrimethylene group, 1-ethyl-2-methyltrimethylene group, 1,1,2-trimethyltrimethylene group,
1,1,3-trimethyltrimethylene group, 1-ethyltetramethylene group, 1,1-dimethyltetramethylene group,
1,3-dimethyltetramethylene group, 1,4-dimethyltetramethylene group, 2,2-dimethyltetramethylene group, 1-methylpentamethylene group, 2-methylpentamethylene group, hexamethylene group (above 6 carbon atoms) Are included. Considering the compatibility between the component (B) and the component (A), R 3 in the formula (1) is preferably an alkylene group having 2 to 6 carbon atoms. P in the formula (1) is 1 to
The number is 30 and is preferably in the range of 1-10. Incidentally, in (1) - (R 3 -O) p - is an oxy alkylene group, when p is 2 or more, not only shows a polyoxyalkylene group of a single structure, 2 different structures At least one kind of oxyalkylene group represents a polyoxyalkylene group which is randomly copolymerized, alternating copolymerized or block copolymerized.

【0008】本発明で使用可能な含酸素化合物の中にあ
って、(1)式におけるR1 が水素、炭素数1〜6の直
鎖または分枝アルキル基、フェニル基および炭素数7〜
15の直鎖または分枝アルキルアリール基のいずれかで
あり、R2 が水素であり、R3 は炭素数2〜6のアルキ
レン基であり、pが1〜10の範囲にある含酸素化合物
は、水との相溶性が優れている点で好ましい。そうした
好ましい含酸素化合物の具体例を例示すると、 :エチレングリコール、プロピレングリコール(全て
の異性体を含む)、ブチレングリコール(全ての異性体
を含む)、ペンチレングリコール(全ての異性体を含
む)、ヘキシリレングリコール(全ての異性体を含む)
などのグリコール :のグリコールの中から選ばれる1種のグリコール
の単独重合ポリグリコール(例えば、ジグリコール、ト
リグリコール、テトラグリコールなどのポリグリコー
ル) :のグリコールの中から選ばれる2種以上のグリコ
ールのランダム共重合体、交互共重合体またはブロック
共重合体などの共重合ポリグリコール(例えば、ポリオ
キシエチレンオキシプロピレングリコールなど) :〜の中から選ばれるグリコールまたはポリグリ
コールのモノアルキルエーテル化物(アルキル基は炭素
数1〜6の直鎖または分枝アルキル基) :〜の中から選ばれるグリコールまたはポリグリ
コールのモノフェニルエーテル化物 :〜の中から選ばれるグリコールまたはポリグリ
コールのモノアルキルフェニルエーテル化物(アルキル
基は炭素数1〜9の直鎖または分枝アルキル基) :〜の中から選ばれる2種以上の化合物の混合物
を挙げることができる。なお、上記の共重合ポリグリ
コールとしては、エチレングリコールとこれ以外のアル
キレングリコールの共重合体であって、当該共重合体を
構成するエチレングリコール対他のアルキレングリコー
ルのモル比が、1〜9対9〜1、好ましくは2〜8対8
〜2の範囲にある共重合ポリグリコールは、水への溶解
性が優れているので、本発明の(B)成分として好まし
い。また、本発明の(B)成分には上記(1)式に包含
される全ての含酸素化合物が使用可能であるが、そうし
た含酸素化合物でも水への溶解性は個々に相違する。一
般的に言えば、(1)式で規定される含酸素化合物の中
でも、後述する添加量で水に添加した場合に均一な溶液
状態になる含酸素化合物が、(B)成分として最も望ま
しく、均一な溶液状態になり難い含酸素化合物を(B)
成分として使用した場合は、圧延加工後の金属材料の表
面の光沢が損なわれる傾向がある。
Among the oxygen-containing compounds usable in the present invention, R 1 in the formula (1) is hydrogen, a linear or branched alkyl group having 1 to 6 carbon atoms, a phenyl group and 7 to 7 carbon atoms.
15 is a linear or branched alkylaryl group, R 2 is hydrogen, R 3 is an alkylene group having 2 to 6 carbon atoms, and the oxygen-containing compound having p in the range of 1 to 10 is It is preferable because it has excellent compatibility with water. Specific examples of such preferable oxygen-containing compounds include: ethylene glycol, propylene glycol (including all isomers), butylene glycol (including all isomers), pentylene glycol (including all isomers), Hexylylene glycol (including all isomers)
Homopolymerization of one kind of glycol selected from glycols such as: Polyglycol (eg, polyglycol such as diglycol, triglycol, tetraglycol): Two or more kinds of glycol selected from glycols Copolymerized polyglycol such as random copolymer, alternating copolymer or block copolymer (for example, polyoxyethyleneoxypropylene glycol): A glycol selected from among or a monoalkyl ether compound of polyglycol (alkyl group) Is a linear or branched alkyl group having 1 to 6 carbon atoms): A monophenyl ether compound of glycol or polyglycol selected from: Monoalkyl phenyl ether compound of glycol or polyglycol selected from (alkyl) The base is carbon 1-9 linear or branched alkyl group) and a mixture of two or more compounds selected from the ~. The above copolymerized polyglycol is a copolymer of ethylene glycol and an alkylene glycol other than ethylene glycol, and the molar ratio of ethylene glycol to the other alkylene glycol constituting the copolymer is 1 to 9: 9-1, preferably 2-8: 8
The copolymerized polyglycol in the range of ˜2 has excellent solubility in water and is therefore preferred as the component (B) of the present invention. Further, although all the oxygen-containing compounds included in the above formula (1) can be used as the component (B) of the present invention, even such oxygen-containing compounds have different solubility in water. Generally speaking, among the oxygen-containing compounds defined by the formula (1), an oxygen-containing compound which becomes a uniform solution state when added to water in an addition amount described later is most desirable as the component (B), An oxygen-containing compound that is difficult to form a uniform solution (B)
When used as a component, the gloss of the surface of the metal material after rolling tends to be impaired.

【0009】本発明の潤滑剤組成物における(B)成分
の含有量の下限は、組成物全量基準で10質量%、好ま
しくは20質量%、より好ましくは30質量%であり、
上限は同じく組成物全量基準で94.95質量%、好ま
しく84.9質量%、よりこのましくは74.8質量%
である。(B)成分の含有量が10質量%未満の場合は
潤滑性が悪化し、94.95質量%を越える場合は圧延
加工後の金属材料表面の光沢が悪化する。本発明の潤滑
剤組成物にあっては、(A)成分と(B)成分の合計含
有量が所定の範囲にあることも重要であって、この合計
含有量の下限は組成物全量基準で80質量%、好ましく
は90質量%、より好ましくは95質量%である。また
その上限は同じく組成物全量基準で99.95質量%、
このましくは99.9質量%、より好ましくは99.8
質量%である。上記の合計含有量が80質量%未満の場
合は圧延加工後の金属材料表面の光沢が悪化し、99.
95質量%を越えた場合は潤滑性が悪化する。
The lower limit of the content of the component (B) in the lubricant composition of the present invention is 10% by mass, preferably 20% by mass, more preferably 30% by mass, based on the total amount of the composition.
The upper limit is also 94.95% by mass, preferably 84.9% by mass, more preferably 74.8% by mass, based on the total amount of the composition.
Is. When the content of the component (B) is less than 10% by mass, the lubricity deteriorates, and when it exceeds 94.95% by mass, the gloss of the surface of the metal material after rolling deteriorates. In the lubricant composition of the present invention, it is also important that the total content of the components (A) and (B) is within a predetermined range, and the lower limit of this total content is based on the total amount of the composition. It is 80% by mass, preferably 90% by mass, more preferably 95% by mass. The upper limit is 99.95% by mass based on the total amount of the composition,
This is preferably 99.9% by mass, more preferably 99.8.
It is% by mass. If the total content is less than 80% by mass, the gloss of the surface of the metal material after rolling is deteriorated, and 99.
If it exceeds 95% by mass, the lubricity deteriorates.

【0010】本発明の(C)成分として使用される脂肪
酸塩は、下記の(a)〜(c)から選ばれる。 (a)炭素数6〜22の脂肪酸のアルカリ金属塩 (b)炭素数6〜22の脂肪酸と、炭素数1〜15のア
ルカノールアミンとの塩 (c)炭素数6〜22の脂肪酸と、下記の(2)式で表
される含窒素化合物との塩 [ここで、R4 は炭素数1〜24の炭化水素基を示し、
5 はエチレン基又はプロピレン基を示し、qは1〜3
0の数を示し、Xは水素、炭素数1〜24の炭化水素基
又は一般式−(R6 −O)r Hで示される基を示し、R
6 はエチレン基又はプロピレン基を示し、rは1〜30
の数を示す。]
The fatty acid salt used as the component (C) of the present invention is selected from the following (a) to (c). (A) Alkali metal salt of fatty acid having 6 to 22 carbon atoms (b) Salt of fatty acid having 6 to 22 carbon atoms and alkanolamine having 1 to 15 carbon atoms (c) Fatty acid having 6 to 22 carbon atoms, and With a nitrogen-containing compound represented by the formula (2) [Here, R 4 represents a hydrocarbon group having 1 to 24 carbon atoms,
R 5 represents an ethylene group or a propylene group, and q is 1 to 3
Represents a number of 0, X represents hydrogen, a hydrocarbon group having 1 to 24 carbon atoms or a group represented by the general formula-(R 6 -O) r H, and R
6 represents an ethylene group or a propylene group, r is 1 to 30
Indicates the number of. ]

【0011】上記の(a)〜(c)で示す各脂肪酸塩を
構成する脂肪酸は、その炭素数が6〜22である限り、
飽和脂肪酸でも不飽和脂肪酸でもよく、また直鎖脂肪酸
でも分枝脂肪酸でもよい。脂肪酸塩を構成する脂肪酸の
具体例としては、ヘキサン酸、ヘプタン酸、オクタン
酸、ノナン酸、デカン酸、ウンデカン酸、ドデカン酸、
トリデカン酸、テトラデカン酸、ペンタデカン酸、ヘキ
サデカン酸、ヘプタデカン酸、オクタデカン酸、ノナデ
カン酸、イコサン酸、ヘンイコサン酸、ドコサン酸など
の各々の直鎖状および分枝状飽和脂肪酸;ヘキセン酸、
ヘプテン酸、オクテン酸、ノネン酸、デセン酸、ウンデ
セン酸、ドデセン酸、トリデセン酸、テトラデセン酸、
ペンタデセン酸、ヘキサデセン酸、ヘプタデセン酸、オ
クタデセン酸、ノナデセン酸、イコセン酸、ヘンイコセ
ン酸、ドコセン酸などの各々の直鎖状および分枝状不飽
和脂肪酸を挙げることができる。なかでも、塩を形成し
た場合の水への溶解度を考慮すると、炭素数10〜18
の直鎖状飽和脂肪酸、分枝状飽和脂肪酸、直鎖状不飽和
脂肪酸及び分枝状不飽和脂肪酸が好ましく、特に、n−
ドデカン酸(ラウリン酸)、n−トリデカン酸、n−テ
トラデカン酸(ミリスチン酸)、n−ペンタデカン酸、
n−ヘキサデカン酸(パルミチン酸)、n−ヘプタデカ
ン酸、n−オクタデカン酸(ステアリン酸)、n−ドデ
セン酸、n−トリデセン酸、n−テトラデセン酸、n−
ペンタデセン酸、n−ヘキサデセン酸、n−ヘプタデセ
ン酸、n−オクタデセン酸(オレイン酸)などの直鎖状
飽和脂肪酸および直鎖状不飽和脂肪酸が好ましい。この
ことは本発明の脂肪酸塩を構成する塩基成分がアルカリ
金属である場合、アルカノールアミンである場合および
(2)式で示す含窒素化合物である場合に共通する。
The fatty acids constituting the fatty acid salts shown in the above (a) to (c) are as long as they have 6 to 22 carbon atoms.
It may be a saturated fatty acid or an unsaturated fatty acid, and may be a straight chain fatty acid or a branched fatty acid. Specific examples of fatty acids constituting the fatty acid salt include hexanoic acid, heptanoic acid, octanoic acid, nonanoic acid, decanoic acid, undecanoic acid, dodecanoic acid,
Linear and branched saturated fatty acids such as tridecanoic acid, tetradecanoic acid, pentadecanoic acid, hexadecanoic acid, heptadecanoic acid, octadecanoic acid, nonadecanoic acid, icosanoic acid, heniicosanoic acid, and docosanoic acid; hexenoic acid,
Heptenoic acid, octenoic acid, nonenic acid, decenoic acid, undecenoic acid, dodecenoic acid, tridecenoic acid, tetradecenoic acid,
Mention may be made of respective straight chain and branched unsaturated fatty acids such as pentadecenoic acid, hexadecenoic acid, heptadecenoic acid, octadecenoic acid, nonadecenoic acid, eicosenoic acid, henicosenoic acid and docosenoic acid. Among them, considering the solubility in water when forming a salt, the number of carbon atoms is 10 to 18
Preferred are linear saturated fatty acids, branched saturated fatty acids, linear unsaturated fatty acids and branched unsaturated fatty acids, particularly n-
Dodecanoic acid (lauric acid), n-tridecanoic acid, n-tetradecanoic acid (myristic acid), n-pentadecanoic acid,
n-hexadecanoic acid (palmitic acid), n-heptadecanoic acid, n-octadecanoic acid (stearic acid), n-dodecenoic acid, n-tridecenoic acid, n-tetradecenoic acid, n-
Linear saturated fatty acids and linear unsaturated fatty acids such as pentadecenoic acid, n-hexadecenoic acid, n-heptadecenoic acid, n-octadecenoic acid (oleic acid) are preferred. This is common when the base component constituting the fatty acid salt of the present invention is an alkali metal, an alkanolamine, and a nitrogen-containing compound represented by the formula (2).

【0012】脂肪酸塩(a)の塩基成分はアルカリ金属
であって、そのアルカリ金属には通常ナトリウムかカリ
ウムが選ばれる。脂肪酸塩(A)は1種または2種以上
の上記した脂肪酸と、1種または2種以上のアルカリ金
属との塩であって差し支えない。脂肪酸塩(b)成分の
塩基成分は、炭素数1ないし15のアルカノールアミン
であって、脂肪酸塩(b)も1種または2種以上の上記
した脂肪酸と、1種または2種以上のアルカノールアミ
ンとの塩であって差し支えない。脂肪酸塩(b)の塩基
成分であるアルカノールアミンには、モノメタノールア
ミン、ジメタノールアミン、トリメタノールアミン、モ
ノエタノールアミン、ジエタノールアミン、トリエタノ
ールアミン、モノ−n−プロパノールアミン、モノイソ
プロパノールアミン、ジ−n−プロパノールアミン、ジ
イソプロパノールアミン、トリ−n−プロパノールアミ
ン、トリイソプロパノールアミン、モノブタノールアミ
ン(全ての異性体を含む)、ジブタノールアミン(全て
の異性体を含む)、トルブタノールアミン(全ての異性
体を含む)、モノペンタノールアミン(全ての異性体を
含む)、ジペンタノールアミン(全ての異性体を含
む)、トリペンタノールアミン(全ての異性体を含
む)、モノヘキサノールアミン(全ての異性体を含
む)、ジヘキサノールアミン(全ての異性体を含む)、
モノヘプタノールアミン(全ての異性体を含む)、ジヘ
プタノールアミン(全ての異性体を含む)、モノオクタ
ノールアミン(全ての異性体を含む)などを包含され
る。これらのなかでも、脂肪酸塩(b)の水へ溶解度を
考慮すると、炭素数1〜9のアルカノールアミンが好ま
しい。従って、本発明の脂肪酸塩(b)としては、先に
示した炭素数10〜18の各脂肪酸の少なくとも1種
と、炭素数炭素数1〜9のアルカノールアミンとの塩が
好ましく、特に炭素数12〜18の飽和または不飽和の
直鎖脂肪酸と、炭素数1〜9のアルカノールアミンとの
塩が好ましい。
The base component of the fatty acid salt (a) is an alkali metal, and sodium or potassium is usually selected as the alkali metal. The fatty acid salt (A) may be a salt of one or more types of the above fatty acids and one or more types of alkali metals. The base component of the fatty acid salt (b) component is an alkanolamine having 1 to 15 carbon atoms, and the fatty acid salt (b) is also one or more types of the above fatty acids and one or more types of alkanolamines. It can be a salt with. Alkanolamines that are the base component of the fatty acid salt (b) include monomethanolamine, dimethanolamine, trimethanolamine, monoethanolamine, diethanolamine, triethanolamine, mono-n-propanolamine, monoisopropanolamine, di- n-propanolamine, diisopropanolamine, tri-n-propanolamine, triisopropanolamine, monobutanolamine (including all isomers), dibutanolamine (including all isomers), tolbutanolamine (all (Including isomers), monopentanolamine (including all isomers), dipentanolamine (including all isomers), tripentanolamine (including all isomers), monohexanolamine (all (Including isomers of Iodixanol amine (including all isomers),
It includes monoheptanolamine (including all isomers), diheptanolamine (including all isomers), monooctanolamine (including all isomers) and the like. Among these, alkanolamines having 1 to 9 carbon atoms are preferable in view of the solubility of the fatty acid salt (b) in water. Therefore, as the fatty acid salt (b) of the present invention, a salt of at least one of the above-mentioned fatty acids having 10 to 18 carbon atoms and an alkanolamine having 1 to 9 carbon atoms is preferable, and particularly a carbon number. A salt of a 12-18 saturated or unsaturated straight-chain fatty acid and an alkanolamine having 1-9 carbon atoms is preferable.

【0013】脂肪酸塩(c)の塩基成分は上記の(2)
式で表される含窒素化合物であり、この脂肪酸塩(c)
も1種または2種以上の上記した脂肪酸と、(2)式で
表される1種または2種以上の含窒素化合物との塩であ
って差し支えない。上記した(2)式において、R4
示す炭素数1〜24の炭化水素基には、メチル基、エチ
ル基、n−プロピル基、イソプロピル基、n−ブチル
基、イソブチル基、sec−ブチル基、tert−ブチ
ル基、直鎖または分枝のペンチル基、直鎖または分枝の
ヘキシル基、直鎖または分枝のヘプチル基、直鎖または
分枝のオクチル基、直鎖または分枝のノニル基、直鎖ま
たは分枝のデシル基、直鎖または分枝のウンデシル基、
直鎖または分枝のドデシル基、直鎖または分枝のトリデ
シル基、直鎖または分枝のテトラデシル基、直鎖または
分枝のペンタデシル基、直鎖または分枝のヘキサデシル
基、直鎖または分枝のヘプタデシル基、直鎖または分枝
のオクタデシル基、直鎖または分枝のノナデシル基、直
鎖または分枝のイコシル基、直鎖または分枝のヘンイコ
シル基、直鎖または分枝のドコシル基、直鎖または分枝
のトリコシル基、直鎖または分枝のテトラコシル基など
の各アルキル基;直鎖または分枝のペンテニル基、直鎖
または分枝のオクテニル基、直鎖または分枝のヘキセニ
ル基、直鎖または分枝のヘプテニル基、直鎖または分枝
のオクテニル基、直鎖または分枝のノネニル基、直鎖ま
たは分枝のデセニル基、直鎖または分枝のウンデセニル
基、直鎖または分枝のドデセニル基、直鎖または分枝の
トリデセニル基、直鎖または分枝のテトラデセニル基、
直鎖または分枝のペンタデセニル基、直鎖または分枝の
ヘキサデセニル基、直鎖または分枝のヘプタデセニル
基、直鎖または分枝のオクタデセニル基、直鎖または分
枝のノナデセニル基、直鎖または分枝のイコセニル基、
直鎖または分枝のヘンイコセニル基、直鎖または分枝の
ドコセニル基、直鎖または分枝のトリコセニル基、直鎖
または分枝のテトラコセニル基などの炭素数5〜24の
各アルケニル基;シクロペンチル基、シクロヘキシル
基、シクロヘプチル基などの炭素数5〜7のシクロアル
キル基;メチルシクロペンチル基、ジメチルシクロペン
チル基(全ての置換異性体を含む)、メチルエチルシク
ロペンチル基(全ての置換異性体を含む)、ジエチルシ
クロペンチル基(全ての置換異性体を含む)、メチルシ
クロヘキシル基、ジメチルシクロヘキシル基(全ての置
換異性体を含む)、メチルエチルシクロヘキシル基(全
ての置換異性体を含む)、ジエチルシクロヘキシル基
(全ての置換異性体を含む)、メチルシクロヘプチル
基、ジメチルシクロヘプチル基(全ての置換異性体を含
む)、メチルエチルシクロヘプチル基(全ての置換異性
体を含む)、ジエチルシクロヘプチル基(全ての置換異
性体を含む)などの炭素数6〜11のアルキルシクロア
ルキル基;フェニル基、ナフチル基などのアリール基:
トリル基、キシリル基(全ての置換異性体を含む)、エ
チルフェニル基、直鎖または分枝のプロピルフェニル
基、直鎖または分枝のブチルフェニル基、直鎖または分
枝のペンチルフェニル基、直鎖または分枝のヘキシルフ
ェニル基、直鎖または分枝のヘプチルフェニル基、直鎖
または分枝のオクチルフェニル基、直鎖または分枝のノ
ニルフェニル基、直鎖または分枝のデシルフェニル基、
直鎖または分枝のウンデシルフェニル基、直鎖または分
枝のドデシルフェニル基、直鎖または分枝のトリデシル
フェニル基、直鎖または分枝のテトラデシルフェニル
基、直鎖または分枝のペンタデシルフェニル基、直鎖ま
たは分枝のヘキサデシルフェニル基、直鎖または分枝の
ヘプタデシルフェニル基、直鎖または分枝のオクタデシ
ルフェニル基などの炭素数6〜24のアルキルアリール
基;ベンジル基、フェニルエチル基、フェニルプロピル
基(プルピル基の異性体を含む)、フェニルブチル基
(ブチル基の異性体を含む)、フェニルペンチル基(ペ
ンチル基の異性体を含む)、フェニルヘキシル基(ヘキ
シル基の異性体を含む)などの炭素数7〜12のアリー
ルアルキル基;などが含まれる。そして、R1 が炭素数
1〜18のアルキル基、炭素数5〜18のアルケニル
基、シクロヘキシル基または炭素数7〜11のアルキル
シクロヘキシル基である含窒素化合物は、当該含窒素化
合物と脂肪酸との塩が程よい融点を有し、潤滑剤組成物
調製時の作業性に優れることから、脂肪酸塩(c)の塩
基成分として好ましい。(2)式におけるR5 はエチレ
ン基またはプロピレン基(メチルエチレン基)のいずれ
かであるが、脂肪酸塩(c)の水に対する溶解度を考慮
すると、エチレン基であることが好ましい。(1)式に
おけるqは1〜30の数を示すが、この値は3〜20で
あるのが好ましい。(2)式におけるXは、水素、炭素
数1〜24の炭化水素基または一般式−(R6 −O)r
Hで表される基を示す。ここで、炭素数1〜24の炭化
水素基には、R4 について先に列挙した各炭化水素基が
包含され、これらのなかでも、炭素数1〜18のアルキ
ル基、炭素数5〜18のアルケニル基、シクロヘキシル
基または炭素数7〜11のアルキルシクロヘキシル基が
好ましい。また、一般式−(R6 −O)r HにおけるR
6 はエチレン基またはプロピレン基(メチルエチレン
基)のいずれかであるが、脂肪酸塩(c)の水に対する
溶解度を考慮すると、エチレン基であることが好まし
い。そして、rは1〜30、好ましくは3〜20の数で
ある。
The base component of the fatty acid salt (c) has the above-mentioned (2)
This fatty acid salt (c) is a nitrogen-containing compound represented by the formula:
Also, it may be a salt of one or more kinds of the above fatty acids and one or more kinds of nitrogen-containing compounds represented by the formula (2). In the above formula (2), the hydrocarbon group having 1 to 24 carbon atoms represented by R 4 includes a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, an isobutyl group and a sec-butyl group. , Tert-butyl group, straight-chain or branched pentyl group, straight-chain or branched hexyl group, straight-chain or branched heptyl group, straight-chain or branched octyl group, straight-chain or branched nonyl group A linear or branched decyl group, a linear or branched undecyl group,
Straight-chain or branched dodecyl group, straight-chain or branched tridecyl group, straight-chain or branched tetradecyl group, straight-chain or branched pentadecyl group, straight-chain or branched hexadecyl group, straight-chain or branched Heptadecyl group, straight-chain or branched octadecyl group, straight-chain or branched nonadecyl group, straight-chain or branched icosyl group, straight-chain or branched henicosyl group, straight-chain or branched docosyl group, direct Each alkyl group such as chain or branched tricosyl group, straight chain or branched tetracosyl group; straight chain or branched pentenyl group, straight chain or branched octenyl group, straight chain or branched hexenyl group, direct Chain or branched heptenyl group, straight chain or branched octenyl group, straight chain or branched nonenyl group, straight chain or branched decenyl group, straight chain or branched undecenyl group, straight chain or branched chain Dodecenyl group, straight or branched tridecenyl, straight or branched tetradecenyl,
Straight-chain or branched pentadecenyl group, straight-chain or branched hexadecenyl group, straight-chain or branched heptadecenyl group, straight-chain or branched octadecenyl group, straight-chain or branched nonadecenyl group, straight-chain or branched An icosenyl group of
Each alkenyl group having 5 to 24 carbon atoms such as a straight chain or branched henicosenyl group, a straight chain or branched docosenyl group, a straight chain or branched tricosenyl group, a straight chain or branched tetracosenyl group; a cyclopentyl group, Cycloalkyl group having 5 to 7 carbon atoms such as cyclohexyl group and cycloheptyl group; methylcyclopentyl group, dimethylcyclopentyl group (including all substituted isomers), methylethylcyclopentyl group (including all substituted isomers), diethyl Cyclopentyl group (including all substitution isomers), methylcyclohexyl group, dimethylcyclohexyl group (including all substitution isomers), methylethylcyclohexyl group (including all substitution isomers), diethylcyclohexyl group (all substitutions) (Including isomers), methylcycloheptyl group, dimethylcyclohep Alkylcycloalkyl having 6 to 11 carbon atoms, such as alkyl group (including all substituted isomers), methylethylcycloheptyl group (including all substituted isomers), diethylcycloheptyl group (including all substituted isomers) Alkyl group; aryl group such as phenyl group and naphthyl group:
Tolyl group, xylyl group (including all substituted isomers), ethylphenyl group, linear or branched propylphenyl group, linear or branched butylphenyl group, linear or branched pentylphenyl group, direct A chain or branched hexylphenyl group, a straight chain or branched heptylphenyl group, a straight chain or branched octylphenyl group, a straight chain or branched nonylphenyl group, a straight chain or branched decylphenyl group,
Straight-chain or branched undecylphenyl group, straight-chain or branched dodecylphenyl group, straight-chain or branched tridecylphenyl group, straight-chain or branched tetradecylphenyl group, straight-chain or branched penta An alkylaryl group having 6 to 24 carbon atoms such as a decylphenyl group, a linear or branched hexadecylphenyl group, a linear or branched heptadecylphenyl group, a linear or branched octadecylphenyl group; a benzyl group, Phenylethyl group, phenylpropyl group (including purpyl group isomers), phenylbutyl group (including butyl group isomers), phenylpentyl group (including pentyl group isomers), phenylhexyl group (including hexyl group) C7-12 arylalkyl groups such as isomers) and the like. The nitrogen-containing compound in which R 1 is an alkyl group having 1 to 18 carbon atoms, an alkenyl group having 5 to 18 carbon atoms, a cyclohexyl group, or an alkylcyclohexyl group having 7 to 11 carbons is a compound of the nitrogen-containing compound and a fatty acid. The salt is preferable as the basic component of the fatty acid salt (c) because the salt has an appropriate melting point and the workability in preparing the lubricant composition is excellent. R 5 in the formula (2) is either an ethylene group or a propylene group (methylethylene group), but in view of the solubility of the fatty acid salt (c) in water, it is preferably an ethylene group. Although q in the formula (1) represents a number of 1 to 30, this value is preferably 3 to 20. X in the formula (2) is hydrogen, a hydrocarbon group having 1 to 24 carbon atoms or a general formula-(R 6 -O) r.
A group represented by H is shown. Here, the hydrocarbon group having 1 to 24 carbon atoms includes each of the hydrocarbon groups listed above for R 4 , and among these, an alkyl group having 1 to 18 carbon atoms and a hydrocarbon group having 5 to 18 carbon atoms are included. An alkenyl group, a cyclohexyl group or an alkylcyclohexyl group having 7 to 11 carbon atoms is preferable. Moreover, the general formula - R in (R 6 -O) r H
Although 6 is either an ethylene group or a propylene group (methylethylene group), an ethylene group is preferable in view of the solubility of the fatty acid salt (c) in water. And r is a number of 1 to 30, preferably 3 to 20.

【0014】なお、(2)式で示される含窒素化合物
は、任意に方法で製造することができ、例えば、下記の
一般式(3)で表されるモノアミンまたは一般式(4)
で表されるジアミンと、エチレンオキサイドまたはプロ
ピレンオキサイドとを反応させることにより容易に得る
ことができる。 R4 −NH2 (3) ここで、R4 は(2)式で定義したところと同じ内容を
示し、R7 は(2)式のXについて説明した炭素数1〜
24の炭化水素基と同じ内容を示す。
The nitrogen-containing compound represented by the formula (2) can be produced by any method, for example, a monoamine represented by the following general formula (3) or a general formula (4).
It can be easily obtained by reacting the diamine represented by: with ethylene oxide or propylene oxide. R 4 -NH 2 (3) Here, R 4 has the same content as defined in the formula (2), and R 7 has 1 to 1 carbon atoms described for X in the formula (2).
The same content as the hydrocarbon group of 24 is shown.

【0015】脂肪酸塩(c)の塩基成分としては、R4
およびXが炭素数1〜18の直鎖または分枝アルキル
基、炭素数5〜18の直鎖または分枝アルケニル基、シ
クロヘキシル基または炭素数7〜11のアルキルシクロ
ヘキシル基であり、R5 がエチレン基であり、qが3〜
20の範囲にある含窒素化合物(以下、これを含窒素化
合物(イ)という)が好ましく、このなかでも、R4
よびXが炭素数1〜18の直鎖または分枝アルキル基、
シクロヘキシル基または炭素数7〜9の直鎖または分枝
アルキルシクロヘキシル基であり、R5 がエチレン基で
あり、qが3〜20の範囲にある含窒素化合物(以下、
これを含窒素化合物(ロ)という)が特に好ましい。従
って、本発明の脂肪酸塩(c)としては、このものが適
度な融点を有し、潤滑剤組成物調製時の作業性に優れる
ことから、先に示した炭素数10〜18の各脂肪酸の少
なくとも1種と、上記の含窒素化合物(イ)との塩が好
ましく、特に炭素数12〜18の飽和または不飽和の直
鎖脂肪酸と、上記含窒素化合物(ロ)との塩が好まし
い。
The base component of the fatty acid salt (c) is R 4
And X is a linear or branched alkyl group having 1 to 18 carbon atoms, a linear or branched alkenyl group having 5 to 18 carbon atoms, a cyclohexyl group or an alkylcyclohexyl group having 7 to 11 carbon atoms, and R 5 is ethylene. And q is 3 to
A nitrogen-containing compound in the range of 20 (hereinafter, referred to as nitrogen-containing compound (a)) is preferable, and among these, R 4 and X are linear or branched alkyl groups having 1 to 18 carbon atoms,
A nitrogen-containing compound which is a cyclohexyl group or a linear or branched alkylcyclohexyl group having 7 to 9 carbon atoms, R 5 is an ethylene group, and q is in the range of 3 to 20 (hereinafter,
This is particularly preferable as a nitrogen-containing compound (b). Therefore, as the fatty acid salt (c) of the present invention, this has an appropriate melting point and is excellent in workability at the time of preparing the lubricant composition. A salt of at least one of the above-mentioned nitrogen-containing compounds (a) is preferable, and a salt of a saturated or unsaturated straight chain fatty acid having 12 to 18 carbon atoms and the above-mentioned nitrogen-containing compound (b) is particularly preferable.

【0016】本発明の(C)成分としては、上記した脂
肪酸塩(a)〜(c)のいずれか1種または2種以上が
使用可能である。そして、各脂肪酸塩は脂肪酸と塩基成
分とを個別に水に添加し、系内で塩を形成させても差し
支えない。予め塩を形成させておくか、あるいは系内で
塩を形成させるかに拘りなく、圧延用潤滑剤組成物に配
合される脂肪酸塩の含有量の下限は組成物全量基準で
0.05質量%、好ましくは0.1重量%、より好まし
くは0.2質量%であり、上限は同じく組成物全量基準
で10質量%、好ましくは5重量%、より好ましくは3
質量%である。脂肪酸塩の含有量が、0.05質量%未
満の場合は、潤滑性が悪化し、10重量%を越える場合
は、脂肪酸塩を水に溶解させることが困難になり、圧延
後の金属板表面の光沢が損なわれる。本発明の(C)成
分は、(A),(B)両成分からなる溶液に、完全に溶
解するか、微細に分散するものが好ましい。
As the component (C) of the present invention, any one or more of the above fatty acid salts (a) to (c) can be used. Then, as for each fatty acid salt, a fatty acid and a basic component may be individually added to water to form a salt in the system. Regardless of whether the salt is formed in advance or the salt is formed in the system, the lower limit of the content of the fatty acid salt blended in the lubricant composition for rolling is 0.05% by mass based on the total amount of the composition. , Preferably 0.1% by weight, more preferably 0.2% by weight, and the upper limit is also 10% by weight, preferably 5% by weight, more preferably 3% by weight based on the total amount of the composition.
It is% by mass. When the content of the fatty acid salt is less than 0.05% by mass, the lubricity is deteriorated, and when it exceeds 10% by weight, it becomes difficult to dissolve the fatty acid salt in water, and the surface of the metal plate after rolling The luster of the The component (C) of the present invention is preferably one which is completely dissolved or finely dispersed in a solution comprising both components (A) and (B).

【0017】上記の(A)〜(C)成分を先に規定した
範囲の量で含有する本発明の組成物は、その構成だけで
圧延用潤滑剤として充分その性能を発揮するが、さらに
その性能を向上させる目的で、公知の種々の添加剤の1
種または2種以上を必要に応じて上記の組成物に含有さ
せることができる。そうした添加剤を例示すれば、硫酸
エステル、スルホン酸エステルなどのアニオン系界面活
性剤およびポリオキシエチレン化合物などのノニオン系
界面活性剤;スルホン酸塩、リン酸およびリン酸塩、ホ
ウ素化合物などの錆止め剤;フェノール系、アミン系、
イオウ系、リン系、塩素系の酸化防止剤;ベンゾトリア
ゾールなどの窒素化合物、イオウおよび窒素を含む化合
物などの腐食防止剤;フェノール系、ホルムアルデヒド
供与体化合物、サリチルアニリド系化合物などの防腐
剤;シリコーン油などがある。これらの添加剤を本発明
の組成物に配合する場合は、その総配合量は組成物全量
基準で通常10質量%以下、好ましくは5質量%以下、
より好ましくは2質量%以下である。
The composition of the present invention containing the above-mentioned components (A) to (C) in an amount within the range defined above exhibits sufficient performance as a rolling lubricant by its constitution alone. One of various known additives for the purpose of improving performance.
One kind or two or more kinds can be contained in the above composition as required. Examples of such additives include anionic surfactants such as sulfates and sulfonates and nonionic surfactants such as polyoxyethylene compounds; rust inhibitors such as sulfonates, phosphates and phosphates, and boron compounds. Agents; phenolic, amine-based,
Sulfur-based, phosphorus-based, and chlorine-based antioxidants; nitrogen compounds such as benzotriazole; corrosion inhibitors such as compounds containing sulfur and nitrogen; preservatives such as phenol-based, formaldehyde donor compounds, salicylanilide compounds; silicones There is oil. When these additives are compounded in the composition of the present invention, the total compounding amount is usually 10% by mass or less, preferably 5% by mass or less, based on the total amount of the composition.
It is more preferably 2% by mass or less.

【0018】本発明の圧延用潤滑油組成物に鉱油や炭化
水素系の合成油を配合することは、たとえこれらがエマ
ルション型圧延油や水可溶化型圧延油の基材として用い
られるものであっても、避けるべきである。ちなみに、
本発明の組成物への配合を避けるべき鉱油としては、例
えば、原油を常圧蒸留または減圧蒸留して得られる潤滑
油留分に、溶剤脱歴、溶剤抽出、水素化分解、溶剤脱ろ
う、接触脱ろう、水素化精製、硫酸洗浄、白土処理など
の一つまたは二つ以上の精製処理を施して精製したパラ
フィン系またはナフテン系鉱油が挙げられ、炭化水素系
合成油としては、ポリα−オレフィン油(ポリブテン、
1−オクテンオリゴマー、1−デセンオリゴマーおよび
これらの水素化油など)、アルキルベンゼン油、アルキ
ルナフタレン油などが挙げられる。また、上述したよう
な添加剤も水に溶解または水を連続相とした状態で分散
するものであることが好ましく、上述したような添加剤
の中からこのような性状を有する添加剤を適宜選択する
ことが好ましい。
Mixing a mineral oil or a hydrocarbon-based synthetic oil into the lubricating oil composition for rolling according to the present invention makes it possible to use these as a base material for emulsion-type rolling oil or water-solubilized rolling oil. But you should avoid it. By the way,
Examples of the mineral oil to be incorporated into the composition of the present invention include, for example, a lubricating oil fraction obtained by distilling crude oil under atmospheric pressure or vacuum distillation, solvent dehistory, solvent extraction, hydrocracking, solvent dewaxing, Examples include paraffinic or naphthenic mineral oils refined by one or more purification treatments such as catalytic dewaxing, hydrorefining, sulfuric acid washing, and clay treatment, and hydrocarbon synthetic oils include poly α- Olefin oil (polybutene,
1-octene oligomers, 1-decene oligomers and hydrogenated oils thereof, etc.), alkylbenzene oils, alkylnaphthalene oils and the like. Further, the above-mentioned additives are also preferably those which are dissolved in water or dispersed in a state where water is in a continuous phase, and an additive having such properties is appropriately selected from the above-mentioned additives. Preferably.

【0019】本発明の圧延用潤滑剤組成物において、水
が連続相を形成しない場合並びに鉱油や炭化水素系合成
油を配合した場合は、圧延後の金属板表面に光沢むらが
生じ易い、乳化液(エマルション)の安定性が乏しい、
オイルステインが発生し易い、圧延加工工程で発生した
摩耗粉および摩耗分と油分との凝集で生じたスカムを濾
過除去する際に、油分が減少するなどの不都合を伴う。
In the lubricant composition for rolling of the present invention, when water does not form a continuous phase and when a mineral oil or a hydrocarbon-based synthetic oil is blended, uneven luster is apt to occur on the surface of a metal plate after rolling. The stability of the liquid (emulsion) is poor,
Oil stains are likely to occur, and when the abrasion powder generated in the rolling process and the scum produced by the agglomeration of the abrasion and oil components are removed by filtration, there are disadvantages such that the oil component decreases.

【0020】本発明の潤滑油組成物は、これを圧延油と
して使用している状態において、上記した(A)〜
(C)の3成分を所定の含有量で含有していればよい。
従って、組成物の保管に際しては、所定の組成になるよ
う(A)〜(C)の3成分を配合し、これを使用時まで
保管しておくことができるほか、本発明で規定する含有
量より(A)成分である水の含有量が乏しい組成物を調
製して、これを使用時まで保管し、圧延油として使用す
る際にこの組成物を水で希釈し、本発明で規定する組成
に調整してもよい。
The lubricating oil composition of the present invention, when used as a rolling oil, has the above-mentioned components (A) to (A).
It suffices that the three components of (C) are contained in predetermined contents.
Therefore, when the composition is stored, the three components (A) to (C) can be mixed so as to have a predetermined composition, and the composition can be stored until the time of use. A composition having a lower content of water as the component (A) is prepared, stored until the time of use, and when used as a rolling oil, this composition is diluted with water to obtain the composition defined in the present invention. You may adjust to.

【0021】[0021]

【発明の効果】本発明の圧延用潤滑剤組成物は、その成
分の大部分が非可燃性で、しかも冷却性に富んだ水で占
められているため、高速圧延工程に使用しても安全性が
高く、また、特殊な脂肪酸塩を含有しているため、優れ
た圧延性を発揮する。また、本発明の圧延用潤滑剤組成
物は、貯蔵安定性が良好で、圧延後の金属板表面に光沢
むらやオイルステインを発生させることがなく、圧延加
工工程で発生した摩耗粉および摩耗分と油分との凝集で
生じたスカムを濾過除去する際に、油分が減少すること
もない。従って、本発明の圧延用潤滑剤組成物は、ステ
ンレス鋼を初めとして、銅、アルミニウム並びにこれら
の合金などを冷間圧延する際の潤滑油として、あるいは
アルミニウムおよびアルミニウム合金などを熱間圧延す
る際の潤滑油として、優れた適性を備え、特に、圧延後
の金属板表面に良好な光沢を付与できる点で、冷間圧延
用潤滑剤に用いて好適である。
INDUSTRIAL APPLICABILITY Since most of the components of the lubricant composition for rolling of the present invention are non-combustible and have a good cooling property, it is safe to use in a high speed rolling process. Since it has high rolling property and contains a special fatty acid salt, it exhibits excellent rolling property. Further, the rolling lubricant composition of the present invention has good storage stability, does not generate uneven gloss or oil stain on the surface of the metal plate after rolling, and wear powder and wear components generated in the rolling step. When the scum generated by the coagulation of the oil and the oil is removed by filtration, the oil does not decrease. Therefore, the rolling lubricant composition of the present invention is used as a lubricating oil for cold rolling of stainless steel, copper, aluminum and alloys thereof, or for hot rolling of aluminum and aluminum alloys. It is suitable for use as a lubricant for cold rolling, because it has excellent suitability as a lubricating oil, and in particular it can impart good gloss to the surface of a metal plate after rolling.

【0022】[0022]

【実施例】以下実施例および比較例を示して本発明をさ
らに具体的に説明するが、本発明はこれら実施例に限定
されるものではない。下記の組成で実施例および比較例
の各潤滑剤組成物を調製した。 実施例1 上水道水 25.8質量% ジエチレングリコール 74.0質量% (小計) 99.8質量% オレイン酸ナトリウム塩 0.2質量% 実施例2 上水道水 39.0質量% ジプロピレングリコール 60.0質量% (小計) 99.0質量% オレイン酸トリエタノールアミン塩 1.0質量% 実施例3 上水道水 29.5質量% ヘキシレングリコール(注1参照) 70.0質量% (小計) 99.5質量% オレイン酸とジシクロヘキシルアミンエチレン オキシド付加物(付加モル数20)との塩 0.5質量% (注1)(2−メチル−2,4−ペンタンジオールが主成分) 実施例4 上水道水 25.5質量% トリプロピレングリコール 74.0質量% (小計) 99.5質量% ラウリン酸とオレイルアミンエチレン オキシド付加物(注2参照) 0.5質量% 実施例5 上水道水 69.8質量% ポリオキシエチレンオキシプロピレングリ コールモノn−ブチルエーテル(注3参照)30.0質量% (小計) 99.8質量% オレイン酸ナトリウム塩 0.2質量% (注3) n−C49 O−(OE−OP)2 −H ここで、−(OE−OP)2 −はオキシエチレン基1モ
ルとオキシプロピレン基1モルのランダム共重合を示
す。 実施例6 上水道水 49.0質量% ポリオキシエチレンオキシプロピレングリ コールモノn−ブチルエーテル(注3参照)50.0質量% (小計) 99.0質量% ラウリン酸ジエタノールアミン塩 1.0質量% 実施例7 上水道水 69.0質量% ポリオキシエチレンオキシプロピレングリ コールモノn−ブチルエーテル(注4参照)30.0質量% (小計) 99.0質量% オレイン酸ジエタノールアミン塩 1.0質量% (注4) n−C49 O−(OE−OP)12−H ここで、−(OE−OP)12−はオキシエチレン基6モ
ルとオキシプロピレン基6モルのランダム共重合を示
す。 実施例8 上水道水 79.0質量% ポリオキシエチレンオキシプロピレングリ コールモノn−ブチルエーテル(注4参照)20.0質量% (小計) 99.0質量% オレイン酸トリエタノールアミン塩 1.0質量% 比較例1 上水道水 99.8質量% オレイン酸ナトリウム塩 0.2質量% 比較例2 上水道水 26.0質量% ジエチレングリコール 74.0質量% 比較例3 上水道水 25.8質量% ジエチレングリコール 44.0質量% オレイン酸ナトリウム塩 0.2質量% ブチルステアレート 30.0質量% 比較例4 パラフィン系精製鉱油 84.4質量% (動粘度7mm2/s@40℃) ブチルステアレート 15.0質量% アルケニルコハク酸エステル 0.6質量% 比較例5 パラフィン系精製鉱油 49.4質量% (動粘度7mm2/s@40℃) ジオクチルセバケート 50.0質量% アルケニルコハク酸エステル 0.6質量% 比較例6 上水道水 90.0質量% パラフィン系精製鉱油 7.3質量% (動粘度7mm2/s@40℃) ブチルステアレート 1.5質量% ポリオキシエチレングリコール モノノニルフェニルエーテル 0.6質量% 石油スルフォン酸ナトリウム塩 0.6質量% 比較例7 上水道水 20.0質量% ジエチレングリコール 1.5質量% パラフィン系精製鉱油 57.0質量% (動粘度7mm2/s@40℃) ポリオキシエチレングリコール モノノニルフェニルエーテル 10.0質量% 石油スルフォン酸ナトリウム塩 10.0質量% オレイン酸 1.5質量% 上記の各潤滑油組成物を用いて下記の圧延加工試験を行
い、その圧延性および圧延加工後の金属板表面の光沢を
評価した。結果を表1に示す。 [圧延加工試験] 圧延条件 圧延材:SUS430 2B材 厚さ0.5mm×幅
50mm ワークロール径:51mmφ ワークロール粗さ:
Ra 0.03μm 圧延速度:100m/min 圧下率:25% (但し、圧延性の評価に当っては、圧下率を順次上昇さ
せた。) 油供給方法:圧延ロールの手前で、ノズルを用いて被圧
延材および圧延ロールに上記の潤滑油組成物を個々に噴
霧した。 評価方法 光沢性:上記の圧延条件で3回圧延した後の圧延材の表
面光沢を、SMカラーコンピュータ(型式SM−2:ス
ガ試験機(株)製)により、裏面直角60°でのグロス
値を測定した。 圧延性:上記の圧延条件で3回圧延した後、4回目の圧
延において圧下率30%で圧延を開始し、その後逐次圧
下率を上げて圧延し、圧延可能な最大圧下率を求めた。 表1 潤滑剤組成物 光沢性% 圧延性% 備 考 実施例 1 480 60 2 500 60 3 500 60 4 480 60 5 520 58 6 520 58 7 520 60 8 480 58 比較例 1 480 42 含酸素化合物無含有 2 380 45 脂肪酸塩無含有 3 400 45 (注5参照) 4 450 42 鉱油系圧延油 5 450 44 鉱油/合成油系圧延油 6 380 40 エマルション型圧延油 7 380 40 水可溶化型圧延油 (注5)水+含酸素化合物の合計含有量が本発明の規定範囲を逸脱している。
EXAMPLES The present invention will be described in more detail with reference to the following examples and comparative examples, but the present invention is not limited to these examples. Lubricant compositions of Examples and Comparative Examples were prepared with the following compositions. Example 1 Tap water 25.8 mass% Diethylene glycol 74.0 mass% (subtotal) 99.8 mass% Oleic acid sodium salt 0.2 mass% Example 2 Tap water 39.0 mass% Dipropylene glycol 60.0 mass % (Subtotal) 99.0% by mass Oleic acid triethanolamine salt 1.0% by mass Example 3 Tap water 29.5% by mass Hexylene glycol (see Note 1) 70.0% by mass (Subtotal) 99.5% by mass % Salt of oleic acid and dicyclohexylamine ethylene oxide adduct (20 moles added) 0.5% by mass (Note 1) (2-methyl-2,4-pentanediol is the main component) Example 4 Tap water 25. 5% by mass Tripropylene glycol 74.0% by mass (subtotal) 99.5% by mass Lauric acid and oleylamine ethylene oxide adduct (Note 2) Reference) 0.5 mass% Example 5 Tap water 69.8% by mass Polyoxyethylene oxypropylene glycol mono-n-butyl ether (see Note 3) 30.0% by mass (subtotal) 99.8% by mass Sodium oleate 0.2% by mass (Note) 3) n-C 4 H 9 O- (OE-OP) 2 -H where, - (OE-OP) 2 - represents a random copolymer of 1 mole and oxypropylene group 1 mole oxyethylene groups. Example 6 Water for tap water 49.0% by mass Polyoxyethylene oxypropylene glycol mono-n-butyl ether (see Note 3) 50.0% by mass (subtotal) 99.0% by mass Diethanolamine salt of lauric acid 1.0% by mass Example 7 Tap water 69.0 mass% Polyoxyethylene oxypropylene glycol mono-n-butyl ether (see note 4) 30.0 mass% (subtotal) 99.0 mass% Oleic acid diethanolamine salt 1.0 mass% (note 4) n-C 4 H 9 O- ( OE-OP) 12 -H where, - (OE-OP) 12 - shows a random copolymer of 6 moles oxyethylene group 6 moles of oxypropylene groups. Example 8 Tap water 79.0 mass% Polyoxyethylene oxypropylene glycol mono-n-butyl ether (see Note 4) 20.0 mass% (subtotal) 99.0 mass% Oleic acid triethanolamine salt 1.0 mass% Comparative example 1 Tap water 99.8 mass% Oleic acid sodium salt 0.2 mass% Comparative example 2 Tap water 26.0 mass% Diethylene glycol 74.0 mass% Comparative example 3 Tap water 25.8 mass% Diethylene glycol 44.0 mass % Sodium oleate 0.2 wt% Butyl stearate 30.0 wt% Comparative Example 4 Paraffin refined mineral oil 84.4 wt% (Kinematic viscosity 7 mm 2 / s @ 40 ° C) Butyl stearate 15.0 wt% Alkenyl succinate 0.6 wt% Comparative example 5 paraffinic refined mineral oil 49.4% by weight (kinematic viscosity 7mm 2 / s @ 40 ℃) Dioctyl sebacate 50.0 wt% alkenyl succinic ester 0.6 wt% Comparative Example 6 tap water 90.0 wt% paraffinic refined mineral oil 7.3 wt% (kinematic viscosity 7mm 2 / s @ 40 ℃) Butyl stearate 1.5 mass% polyoxyethylene glycol monononylphenyl ether 0.6 mass% petroleum sulfonic acid sodium salt 0.6 mass% Comparative Example 7 tap water 20.0 mass% diethylene glycol 1.5 mass% paraffinic refined mineral oil 57. 0% by mass (kinematic viscosity 7 mm 2 / s @ 40 ° C) Polyoxyethylene glycol monononylphenyl ether 10.0% by mass Petroleum sulfonic acid sodium salt 10.0% by mass Oleic acid 1.5% by mass Each of the above lubricating oil compositions Using the product, the following rolling test was conducted to evaluate the rolling property and the gloss of the surface of the metal plate after the rolling. The results are shown in Table 1. [Rolling processing test] Rolling conditions Rolled material: SUS430 2B material Thickness 0.5 mm x width 50 mm Work roll diameter: 51 mm φ Work roll roughness:
Ra 0.03 μm Rolling speed: 100 m / min Reduction ratio: 25% (However, in the evaluation of rollability, the reduction ratio was sequentially increased.) Oil supply method: Before the rolling roll, using a nozzle The above-mentioned lubricating oil composition was individually sprayed onto the material to be rolled and the rolling roll. Evaluation method Gloss: The surface gloss of the rolled material after being rolled three times under the above-mentioned rolling conditions was measured by a SM color computer (model SM-2: manufactured by Suga Test Instruments Co., Ltd.) at a gloss value at a right angle of 60 ° on the back surface. Was measured. Rollability: After rolling three times under the above-mentioned rolling conditions, rolling was started at a rolling reduction of 30% in the fourth rolling, and then rolling was performed by successively increasing the rolling reduction to obtain the maximum rolling reduction possible. Table 1 Lubricant composition Gloss %% Rollability % Remarks Example 1 480 60 2 500 603 3 500 604 4 480 60 5 520 58 6 6 520 58 7 520 608 8 480 58 58 Comparative Example 1 480 42 No oxygen-containing compound 2 380 45 Fatty acid salt-free 3 400 45 (See Note 5) 4 450 42 Mineral oil rolling oil 5 450 44 Mineral oil / Synthetic oil rolling oil 6 380 40 Emulsion rolling oil 7 380 40 Water-solubilized rolling oil (Note) 5) The total content of water and oxygen-containing compounds is out of the specified range of the present invention.

【0023】表1に示す試験結果から明らかな通り、本
発明に係る実施例1〜8の潤滑剤組成物は、いずれも圧
延加工後の金属板の表面の光沢に良好で、圧延性にも優
れている。これに対し、比較例1〜7の潤滑剤組成物
は、実施例1〜8の潤滑剤組成物に比較して光沢性およ
び圧延性が劣っている。
As is clear from the test results shown in Table 1, all of the lubricant compositions of Examples 1 to 8 according to the present invention had a good gloss on the surface of the metal plate after the rolling process and had a good rolling property. Are better. On the other hand, the lubricant compositions of Comparative Examples 1 to 7 are inferior in glossiness and rollability to the lubricant compositions of Examples 1 to 8.

フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 C10M 107:34 125:14 129:32 129:40 145:26) C10N 30:06 40:24 Z (72)発明者 柴田 潤一 横浜市中区千鳥町8番地 日本石油株式会 社中央技術研究所内 (72)発明者 夏目 芳孝 横浜市中区千鳥町8番地 日本石油株式会 社中央技術研究所内Continuation of the front page (51) Int.Cl. 6 Identification number Office reference number FI technical display location C10M 107: 34 125: 14 129: 32 129: 40 145: 26) C10N 30:06 40:24 Z (72) Inventor Junichi Shibata 8 Chidoricho, Naka-ku, Yokohama-shi Central Research Institute of Petroleum Corporation (72) Inventor Yoshitaka Natsume 8 Chidori-cho, Naka-ku Yokohama-shi Central Research Institute of Petroleum

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 組成物全量基準で、 (A)水 5〜89.95質量%、 (B)下記の(1)式で表される含酸素化合物 10〜94.95質量%、 R1 O−(R3 −O)p −R2 (1) [ここで、R1 およびR2 はそれぞれ個別に水素または炭素数1〜18の炭 化水素基を示し、R3 は炭素数1〜6のアルキレン基を示し、pは1〜 30の数を示す。] (C)下記の(a)〜(c)から選ばれる少なくとも1種の脂肪酸塩 0.05〜10質量%、 (a)炭素数6〜22の脂肪酸のアルカリ金属塩 (b)炭素数6〜22の脂肪酸と、炭素数1〜15のアルカノールアミン との塩 (c)炭素数6〜22の脂肪酸と、下記の(2)式で表される含窒素化合 物との塩 [ここで、R4 は炭素数1〜24の炭化水素基を示し、
5 はエチレン基又はプロピレン基を示し、qは1〜3
0の数を示し、Xは水素、炭素数1〜24の炭化水素基
又は一般式−(R6 −O)r Hで示される基を示し、 R6 はエチレン基又はプロピレン基を示し、rは1〜3
0の数を示す。]を含有し、上記(1)式で表した含酸
素化合物および水の合計含有量が、組成物全量基準で8
0〜99.95質量%であることを特徴とする圧延用潤
滑剤組成物。
1. Based on the total amount of the composition, (A) water 5 to 89.95% by mass, (B) oxygen-containing compound represented by the following formula (1) 10 to 94.95% by mass, R 1 O - (R 3 -O) p -R 2 (1) [ wherein, R 1 and R 2 each independently represents hydrogen or coal hydrocarbon group having 1 to 18 carbon atoms, R 3 is 1 to 6 carbon atoms Is an alkylene group, and p is a number from 1 to 30. ] (C) At least one fatty acid salt selected from the following (a) to (c): 0.05 to 10% by mass, (a) Alkali metal salt of a fatty acid having 6 to 22 carbon atoms (b) 6 carbon atoms To a fatty acid having 22 to 22 carbon atoms and an alkanolamine having 1 to 15 carbon atoms (c) a salt having 6 to 22 carbon atoms and a nitrogen-containing compound represented by the following formula (2) [Here, R 4 represents a hydrocarbon group having 1 to 24 carbon atoms,
R 5 represents an ethylene group or a propylene group, and q is 1 to 3
0 represents the number of 0, X represents hydrogen, a hydrocarbon group having 1 to 24 carbon atoms or a group represented by the general formula — (R 6 —O) r H, R 6 represents an ethylene group or a propylene group, and r Is 1-3
Indicates the number of zeros. ], The total content of the oxygen-containing compound represented by the above formula (1) and water is 8 based on the total amount of the composition.
A lubricant composition for rolling, characterized in that it is 0 to 99.95% by mass.
JP31116994A 1994-11-21 1994-11-21 Rolling lubricant composition Expired - Fee Related JP3406407B2 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
JP31116994A JP3406407B2 (en) 1994-11-21 1994-11-21 Rolling lubricant composition
EP95850199A EP0712925A3 (en) 1994-11-21 1995-11-10 Lubricating oil composition
TW084112004A TW294716B (en) 1994-11-21 1995-11-14
KR1019950042207A KR100423478B1 (en) 1994-11-21 1995-11-20 Lubricant Composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
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JP3406407B2 JP3406407B2 (en) 2003-05-12

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US10519391B2 (en) 2017-08-17 2019-12-31 Dane Bush Gun lubricant

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3580847A (en) * 1967-06-16 1971-05-25 Wyandotte Chemicals Corp Hydraulic fluid
US4243537A (en) * 1978-08-08 1981-01-06 Aluminum Company Of America Synthetic metal working lubricant
US4452712A (en) * 1983-01-20 1984-06-05 Aluminum Company Of America Metalworking with an aqueous synthetic lubricant containing polyoxypropylene-polyoxyethylene-polyoxypropylene block copolymers
SE452627B (en) * 1986-05-13 1987-12-07 Berol Suisse Sa PROCEDURES FOR MECHANICAL PROCESSING OF METALS IN THE PRESENT OF A WATER BASED COOLANT MORSE AND CONCENTRATE OF THE COOLING MORSE AGENT
US4830768A (en) * 1988-02-22 1989-05-16 Aluminum Company Of America Metalworking lubricant composition containing propoxylated fatty alcohol
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TW294716B (en) 1997-01-01
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EP0712925A2 (en) 1996-05-22
JP3406407B2 (en) 2003-05-12

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