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JPH0329277B2 - - Google Patents

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Publication number
JPH0329277B2
JPH0329277B2 JP60073579A JP7357985A JPH0329277B2 JP H0329277 B2 JPH0329277 B2 JP H0329277B2 JP 60073579 A JP60073579 A JP 60073579A JP 7357985 A JP7357985 A JP 7357985A JP H0329277 B2 JPH0329277 B2 JP H0329277B2
Authority
JP
Japan
Prior art keywords
lubricating oil
oil composition
weight
dicarboxylic acid
conducted
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.)
Expired - Lifetime
Application number
JP60073579A
Other languages
Japanese (ja)
Other versions
JPS61233091A (en
Inventor
Tadashi Katabuchi
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 JP7357985A priority Critical patent/JPS61233091A/en
Publication of JPS61233091A publication Critical patent/JPS61233091A/en
Publication of JPH0329277B2 publication Critical patent/JPH0329277B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】[Detailed description of the invention]

〔産業上の利用分野〕 本発明は潤滑油組成物に関し、詳しくは潤滑性
が向上し、しかも摩擦面や加工面の外観を低下さ
せることがなく、特に圧延,絞り,打抜き,切削
等の金属加工に有効に用いることのできる潤滑油
組成物に関する。 〔従来技術及び発明が解決しようとする問題点〕 潤滑油には各種の油性剤,極圧剤が配合されて
使用されており、耐焼付性や耐摩耗性など潤滑性
の向上に貢献している。 しかしながら、これら従来公知の化合物で潤滑
性向上効果の大きいもの、例えば高脂肪族酸,イ
オウ化合物,リン酸エステル等は摩擦面や加工面
に摩耗粉を主体に錆などの付着したよごれを発生
させ、その外観を悪化させてしまうという問題が
ある。特にこれら化合物を金属加工油として用い
る場合には加工物が商品として販売されるもので
あるため、外観の悪化は商品の価値を著しく低下
させることとなりその解決が望まれている。 〔問題点を解決するための手段〕 本発明者は上記従来の問題点を解消するため鋭
意研究を重ねた。その結果、鉱油および/または
合成物に特定の構造式を有するジカルボン酸また
はその水添物と、特定のアルキルアミンとの反応
により生成する塩を配合した組成物が、摩耗面や
加工面の外観(表面状態)を低下させることがな
く、しかも潤滑性も向上させることを見出し、こ
の知見に基いて本発明を完成するに到つた。 すなわち、本発明は(A)鉱油および/または合成
油及び(B)一般式 〔式中、Xは0または1を示す。〕 または で表わされる脂肪族ジカルボン酸またはその水添
物と総炭素数20〜60の第2級または第3級のアル
キルアミンとの反応による生成する塩からなる潤
滑油組成物を提供するものである。 本発明においては(A)成分として鉱油および/ま
たは合成油を用いる。ここで鉱油および/または
合成油は本発明の潤滑油組成物のベースとなるも
ので、特に制限はないが、40℃の粘度が5〜
100cstのものがよい。具体的には鉱油としてナフ
テン系鉱油,中間系鉱油,パラフイン系鉱油の潤
滑油留分あるいはこれら鉱油類の分解によつて得
られる高芳香族成分などを例示することができ、
合成油として長鎖アルキルベンゼン,分枝アルキ
ルベンゼン、あるいはポリブテンなどのポリオレ
フイン油,アルキルナフタリン,エステル油ある
いはポリグリコール油などを例示することができ
る。これらの中でもパラフイン系鉱油が好まし
い。上述の油は単独であるいは二種類以上を混合
して用いることができる。 また、本発明においては(B)成分として、前記一
般式〔〕または〔〕で表わされる脂肪族ジカ
ルボン酸またはその水添物と、総炭素数20〜60の
第2級または第3級のアルキルアミンとの反応に
より生成する塩を用いる。 ここで上記一般式〔〕または〔〕で表わさ
れる脂肪族ジカルボン酸は、具体的には例えば式 などで表わされるものを挙げることができる。 上記一般式〔〕または〔〕で表わされる脂
肪族ジカルボン酸と反応させるアルキルアミンと
しては、総炭素数が20〜60のものが用いられる。
また、アルキルアミンとしては第2級であると第
3級であるとを問わないが、特に第3級アミンが
好ましい。 このようなアルキルアミンの具体例としては例
えば、ジメチルステアリルアミン,ジメチルオレ
イルアミン,ジラウリルモノメチルアミン,トリ
オクチルアミン,ジステアリルアミン,ジオレイ
ルアミンなどが挙げられる。 上記脂肪族ジカルボン酸とアルキルアミンとの
反応は両者を前者:後者=1:0.2〜10(モル比)、
好ましくは1:0.5〜5(モル比)の割合で使用
し、室温乃至100℃の温度、好ましくは40〜80℃
の温度で5〜150分、好ましくは20〜100分の条件
で行なう。 ただし、このように両者は比較的容易に反応す
るので、組成物を製造する際に、両者を別々に投
入して混合することによつて両者を反応させても
よい。 このような反応生成物は単独で用いてもよく、
2種以上を組合せて用いてもよい。 本発明においてはこのようにして得られる脂肪
族ジカルボン酸とアルキルアミンとの反応生成物
を(B)成分として用いる。この反応生成物は0.01重
量%以上、好ましくは0.5〜30重量%配合される。
ここで、この反応生成物の配合量が0.01重量%未
満であると、本発明の目的を達成することができ
ない。 本発明は基本的には上記(A),(B)両成分からなる
ものであるが、必要に応じて油性剤,極圧剤,酸
化防止剤,増粘剤,金属イオン封鎖剤,流動点降
下剤,防錆剤,消泡剤などを適宜添加して物性の
改良を図ることができる。 本発明の潤滑油組成物は通常、不水用型のもの
であるが、必要に応じて乳化剤を配合してエマル
ジヨン型のものとすることもでき、その用途に応
じて利用することが可能である。 〔発明の効果〕 叙上の如き本発明によれば、摩擦面や加工面に
摩耗粉を主体に錆その他が付着して発生するよご
れにより摩擦面や加工面の表面状態(表面仕上
げ)を低下させる虞れがない。 しかも、本発明の潤滑油組成物は耐焼付性,耐
摩耗性,摩擦係数などの潤滑性能も優れたもので
ある。 このように本発明の潤滑油組成物は潤滑性能に
優れており、しかも摩擦面や加工面の表面仕上げ
を著しく改善したものであり、潤滑油全般、特に
金属加工油として極めて有効に用いることができ
る。 〔実施例〕 次に本発明を実施例により説明する。 製造例 1 式 で表わされる6−エチル−ヘキサデカン−1,16
−ジカルボン酸とジラウリルメチルアミンとを
1:0.5(モル比)の割合で混合し、60℃で50分間
撹拌しながら反応を行ない反応生成物を得た。 製造例 2 製造例1においてジラウリルメチルアミンの代
わりにトリ−n−オクチルアミンを用い、原料の
モル比を前者:後者=1:1としたこと以外は製
造例1と同様にして反応生成物を得た。 製造例 3 式 HOOC(CH218COOH で表わされる1,18−オクタデカメチレンジカル
ボン酸とトリ−2−オクチルアミンとを1:2
(モル比)の割合で混合し、60℃で50分間撹拌し
ながら反応を行ない反応生成物を得た。 製造例 4 製造例1においてジラウリルメチルアミンの代
わりにジオレイルアミンを用い、原料のモル比を
前者:後者=1:5としたこと以外は製造例1と
同様にして反応生成物を得た。 製造例 5 式 で表わされる6−ビニル△9ヘキサデセン−1,
16−ジカルボン酸とジメチルオレイルアミンとを
1:3(モル比)の割合で混合し、60℃で50分間
撹拌しながら反応を行ない反応生成物を得た。 実施例 1 パラフイン系鉱油(15cst(40℃))98重量%,
オレイン酸1重量%および製造例2で得た反応生
成物1重量%を配合して潤滑油組成物を得た。こ
の潤滑油組成物について圧延試験、貯蔵安定性試
験を以下の方法により行なつた。結果を第1表に
示す。 〔圧延試験〕 可逆式精密二段圧延機(吉田第二記念製,ロー
ル寸法200φ×200L,ロール材質SUJ−2,硬度
Hs97,ロール粗さ0.4μRmax)を用いて下記の圧
延条件にて2パス圧延を行ない、ヒートクラツチ
の有無および圧延ロールへの付着物の多少を示す
ロールコーテイングの強弱を評価した。 圧延条件 圧延材:SUS430(1.0mm×50mm×100m) 圧延速度:100m/min 圧下率:30%(1パス)−30%(2パス) 〔貯蔵安定性試験〕 500mlのガラスビンに、潤滑油組成物を採取し、
1日放置して沈澱物発生の有無を観察した。結果
を第1表に示す。 実施例 2 実施例1において、製造例2で得た反応生成物
の代わりに製造例4で得た反応生成物1重量%を
用いたこと以外は実施例1と同様にして潤滑油組
成物を得、圧延試験,貯蔵安定性試験を行なつ
た。結果を第1表に示す。 実施例 3 パラフイン系鉱油(15cst(40℃))90重量%お
よび製造例1で得た反応生成物10重量%を配合し
て潤滑油組成物を得、この潤滑油組成物について
実施例1と同様にして圧延試験,貯蔵安定性試験
を行なつた。結果を第1表に示す。 比較例 1 パラフイン系鉱油(15cst(40℃))95重量%お
よび製造例3で得た反応生成物5重量%を配合し
て潤滑油組成物を得、この潤滑油組成物について
実施例1と同様にして圧延試験,貯蔵安定性試験
を行なつた。結果を第1表に示す。 実施例 4 パラフイン系鉱油(15cst(40℃))98重量%お
よび製造例4で得た反応生成物2重量%を配合し
て潤滑油組成物を得、この潤滑油組成物について
実施例1と同様にして圧延試験,貯蔵安定性試験
を行なつた。結果を第1表に示す。 比較例 2 実施例1で用いたと同じパラフイン系鉱油
(15cst(40℃))について実施例1と同様にして圧
延試験,貯蔵安定性試験を行なつた。結果を第1
表に示す。 比較例 3 パラフイン系鉱油(15cst(40℃))99重量%お
よびオレイン酸1重量%を配合して潤滑油組成物
を得、この潤滑油組成物について実施例1と同様
にして圧延試験,貯蔵安定性試験を行なつた。結
果を第1表に示す。 比較例 4 実施例1で用いたと同じパラフイン系鉱油
(15cst(40℃))99重量%と 式 で表わされる6−エチル−ヘキサデカン−1,16
−ジカルボン酸1.0重量%を配合して潤滑油組成
物を得た。この潤滑油組成物について実施例1と
同様にして圧延試験,貯蔵安定性試験を行なつ
た。結果を第1表に示す。 比較例 5 実施例1で用いたと同じパラフイン系鉱油
(15cst(40℃))99重量%とジラウリルアミン1重
量%を配合して潤滑油組成物を得、この潤滑油組
成物について実施例1と同様にして圧延試験,貯
蔵安定性試験を行なつた。結果を第1表に示す。
[Industrial Application Field] The present invention relates to a lubricating oil composition, and more particularly, the present invention relates to a lubricating oil composition that has improved lubricity and does not deteriorate the appearance of friction surfaces or machined surfaces, and is particularly suitable for use with metals such as rolling, drawing, punching, cutting, etc. The present invention relates to a lubricating oil composition that can be effectively used for processing. [Prior art and problems to be solved by the invention] Lubricating oils contain various oil-based agents and extreme pressure agents, which contribute to improving lubricity such as seizure resistance and wear resistance. There is. However, these conventionally known compounds that have a large effect on improving lubricity, such as high aliphatic acids, sulfur compounds, and phosphoric acid esters, generate dirt on friction surfaces and machined surfaces, mainly consisting of wear particles and rust. , there is a problem in that it deteriorates its appearance. Particularly when these compounds are used as metalworking oils, the processed product is sold as a product, so deterioration in appearance significantly reduces the value of the product, and a solution to this problem is desired. [Means for Solving the Problems] The present inventor has conducted extensive research in order to solve the above-mentioned conventional problems. As a result, a composition containing mineral oil and/or a synthetic compound containing a dicarboxylic acid having a specific structural formula or its hydrogenated product and a salt produced by the reaction with a specific alkyl amine has been found to improve the appearance of worn and machined surfaces. It was discovered that the lubricity was improved without deteriorating the surface condition (surface condition), and based on this knowledge, the present invention was completed. That is, the present invention provides (A) mineral oil and/or synthetic oil and (B) general formula [In the formula, X represents 0 or 1. 〕 or The present invention provides a lubricating oil composition comprising a salt produced by reacting an aliphatic dicarboxylic acid represented by the formula or its hydrogenated product with a secondary or tertiary alkylamine having a total of 20 to 60 carbon atoms. In the present invention, mineral oil and/or synthetic oil is used as component (A). Here, the mineral oil and/or synthetic oil is the base of the lubricating oil composition of the present invention, and is not particularly limited, but has a viscosity of 5 to 5 at 40°C.
100 cst is good. Specifically, mineral oils include naphthenic mineral oils, intermediate mineral oils, lubricating oil fractions of paraffinic mineral oils, and highly aromatic components obtained by decomposition of these mineral oils.
Examples of synthetic oils include long-chain alkylbenzenes, branched alkylbenzenes, polyolefin oils such as polybutene, alkylnaphthalenes, ester oils, and polyglycol oils. Among these, paraffin mineral oil is preferred. The above-mentioned oils can be used alone or in combination of two or more. In addition, in the present invention, as component (B), an aliphatic dicarboxylic acid represented by the above general formula [] or [] or a hydrogenated product thereof, and a secondary or tertiary alkyl having a total number of carbon atoms of 20 to 60. A salt produced by reaction with an amine is used. Here, the aliphatic dicarboxylic acid represented by the above general formula [] or [] is specifically, for example, Examples of such expressions include: As the alkylamine to be reacted with the aliphatic dicarboxylic acid represented by the above general formula [] or [], those having a total carbon number of 20 to 60 are used.
Further, the alkylamine may be either secondary or tertiary, but tertiary amine is particularly preferred. Specific examples of such alkylamines include dimethylstearylamine, dimethyloleylamine, dilaurylmonomethylamine, trioctylamine, distearylamine, dioleylamine, and the like. In the reaction between the aliphatic dicarboxylic acid and the alkylamine, the former: the latter = 1:0.2-10 (molar ratio).
It is preferably used in a ratio of 1:0.5 to 5 (molar ratio), and at a temperature of room temperature to 100°C, preferably 40 to 80°C.
It is carried out at a temperature of 5 to 150 minutes, preferably 20 to 100 minutes. However, since the two react relatively easily in this way, when producing the composition, the two may be added separately and mixed to cause the two to react. Such reaction products may be used alone,
You may use two or more types in combination. In the present invention, the thus obtained reaction product of an aliphatic dicarboxylic acid and an alkylamine is used as component (B). This reaction product is blended in an amount of 0.01% by weight or more, preferably 0.5 to 30% by weight.
Here, if the blending amount of this reaction product is less than 0.01% by weight, the object of the present invention cannot be achieved. The present invention basically consists of both components (A) and (B) above, but if necessary, oily agents, extreme pressure agents, antioxidants, thickeners, sequestering agents, and pour point Physical properties can be improved by appropriately adding depressants, rust preventives, antifoaming agents, etc. The lubricating oil composition of the present invention is usually a water-free type, but if necessary, it can be made into an emulsion type by adding an emulsifier, and can be used depending on the purpose. be. [Effects of the Invention] According to the present invention as described above, the surface condition (surface finish) of the friction surface or machined surface is deteriorated due to dirt generated by adhesion of wear particles mainly rust or other substances to the friction surface or machined surface. There is no risk of it happening. Moreover, the lubricating oil composition of the present invention has excellent lubricating properties such as seizure resistance, wear resistance, and friction coefficient. As described above, the lubricating oil composition of the present invention has excellent lubrication performance and has significantly improved surface finish on friction surfaces and machined surfaces, and can be used extremely effectively as a lubricating oil in general, and as a metalworking oil in particular. can. [Example] Next, the present invention will be explained with reference to an example. Manufacturing example 1 formula 6-ethyl-hexadecane-1,16 represented by
-Dicarboxylic acid and dilaurylmethylamine were mixed at a ratio of 1:0.5 (molar ratio), and the reaction was carried out with stirring at 60°C for 50 minutes to obtain a reaction product. Production Example 2 The reaction product was produced in the same manner as in Production Example 1, except that tri-n-octylamine was used instead of dilaurylmethylamine in Production Example 1, and the molar ratio of the raw materials was set to 1:1. I got it. Production Example 3 1,18-octadecamethylenedicarboxylic acid represented by the formula HOOC(CH 2 ) 18 COOH and tri-2-octylamine were mixed in a ratio of 1:2.
(molar ratio) and reacted at 60°C for 50 minutes with stirring to obtain a reaction product. Production Example 4 A reaction product was obtained in the same manner as in Production Example 1 except that dioleylamine was used instead of dilaurylmethylamine and the molar ratio of the raw materials was 1:5. Manufacturing example 5 formula 6-vinyl△ 9hexadecene -1,
16-dicarboxylic acid and dimethyloleylamine were mixed at a ratio of 1:3 (molar ratio), and the reaction was carried out at 60°C for 50 minutes with stirring to obtain a reaction product. Example 1 Paraffin mineral oil (15cst (40℃)) 98% by weight,
A lubricating oil composition was obtained by blending 1% by weight of oleic acid and 1% by weight of the reaction product obtained in Production Example 2. A rolling test and a storage stability test were conducted on this lubricating oil composition by the following methods. The results are shown in Table 1. [Rolling test] Reversible precision two-high rolling machine (manufactured by Yoshida Daini Kinen, roll size 200φ x 200L, roll material SUJ-2, hardness
Two passes of rolling were performed under the following rolling conditions using Hs97, roll roughness 0.4 μRmax), and the strength of the roll coating, which indicates the presence or absence of heat clutches and the amount of deposits on the rolling rolls, was evaluated. Rolling conditions Rolled material: SUS430 (1.0 mm x 50 mm x 100 m) Rolling speed: 100 m/min Reduction rate: 30% (1 pass) - 30% (2 passes) [Storage stability test] Lubricating oil composition in a 500 ml glass bottle collect things,
The sample was left for one day and observed for the presence or absence of a precipitate. The results are shown in Table 1. Example 2 A lubricating oil composition was prepared in the same manner as in Example 1, except that 1% by weight of the reaction product obtained in Production Example 4 was used instead of the reaction product obtained in Production Example 2. A rolling test and a storage stability test were conducted. The results are shown in Table 1. Example 3 A lubricating oil composition was obtained by blending 90% by weight of paraffinic mineral oil (15cst (40°C)) and 10% by weight of the reaction product obtained in Production Example 1, and this lubricating oil composition was prepared in accordance with Example 1. Rolling tests and storage stability tests were conducted in the same manner. The results are shown in Table 1. Comparative Example 1 A lubricating oil composition was obtained by blending 95% by weight of paraffinic mineral oil (15 cst (40°C)) and 5% by weight of the reaction product obtained in Production Example 3. Rolling tests and storage stability tests were conducted in the same manner. The results are shown in Table 1. Example 4 A lubricating oil composition was obtained by blending 98% by weight of paraffinic mineral oil (15cst (40°C)) and 2% by weight of the reaction product obtained in Production Example 4, and this lubricating oil composition was prepared in accordance with Example 1. Rolling tests and storage stability tests were conducted in the same manner. The results are shown in Table 1. Comparative Example 2 A rolling test and a storage stability test were conducted in the same manner as in Example 1 using the same paraffinic mineral oil (15cst (40°C)) used in Example 1. Results first
Shown in the table. Comparative Example 3 A lubricating oil composition was obtained by blending 99% by weight of paraffin mineral oil (15 cst (40°C)) and 1% by weight of oleic acid, and this lubricating oil composition was subjected to a rolling test and stored in the same manner as in Example 1. A stability test was conducted. The results are shown in Table 1. Comparative Example 4 99% by weight of the same paraffinic mineral oil (15cst (40°C)) used in Example 1 and the formula 6-ethyl-hexadecane-1,16 represented by
- A lubricating oil composition was obtained by blending 1.0% by weight of dicarboxylic acid. A rolling test and a storage stability test were conducted on this lubricating oil composition in the same manner as in Example 1. The results are shown in Table 1. Comparative Example 5 A lubricating oil composition was obtained by blending 99% by weight of the same paraffinic mineral oil (15cst (40°C)) used in Example 1 and 1% by weight of dilaurylamine, and this lubricating oil composition was prepared in Example 1. Rolling tests and storage stability tests were conducted in the same manner as above. The results are shown in Table 1.

〔研削試験〕[Grinding test]

平面研削盤(花村技研(株)製,SG300)を用いて
下記の研削条件にて研削を行ない、砥石回転モー
ターの消費電力と砥石のよごれを評価した。 研削条件 工作物:S45C(HRc55) 研削砥石:WA46J6V1号(150×13) 研削速度:1500m/min 切り込み量:10μm 研削回数:100回 テーブル送り:10m/min 給油量:10/min 実施例 6 実施例5において、製造例2で得た反応生成物
の代わりに製造例5で得た反応生成物1重量%を
用いたこと以外は実施例5と同様にして潤滑油組
成物を得、研削試験,貯蔵安定性試験を行なつ
た。結果を第2表に示す。 比較例 6 実施例5で用いたと同じパラフイン系鉱油
(20cst(40℃))95重量%および塩素化パラフイン
(Cl含量≒40重量%)5重量%を配合して潤滑油
組成物を得、この潤滑油組成物について研削試
験,貯蔵安定性試験を行なつた。結果を第2表に
示す。 比較例 7 実施例5で用いたと同じパラフイン系鉱油
(20cst(40℃))94重量%,塩素化パラフイン(Cl
含量≒40重量%)5重量%および 式 で表わされる6−エチル−ヘキサデカン−1,16
−ジカルボン酸1重量%を配合して潤滑油組成物
を得た。この潤滑油組成物について実施例6と同
様にして研削試験,貯蔵安定性試験を行なつた。
結果を第2表に示す。
Grinding was performed using a surface grinder (SG300, manufactured by Hanamura Giken Co., Ltd.) under the following grinding conditions, and the power consumption of the grindstone rotation motor and the dirt on the grindstone were evaluated. Grinding conditions Workpiece: S45C (HRc55) Grinding wheel: WA46J6V1 (150×13) Grinding speed: 1500m/min Depth of cut: 10μm Number of grinding: 100 times Table feed: 10m/min Lubrication amount: 10/min Example 6 Implementation In Example 5, a lubricating oil composition was obtained in the same manner as in Example 5, except that 1% by weight of the reaction product obtained in Production Example 5 was used instead of the reaction product obtained in Production Example 2, and a grinding test was conducted. , a storage stability test was conducted. The results are shown in Table 2. Comparative Example 6 A lubricating oil composition was obtained by blending 95% by weight of the same paraffinic mineral oil (20cst (40°C)) used in Example 5 and 5% by weight of chlorinated paraffin (Cl content ≒ 40% by weight). Grinding tests and storage stability tests were conducted on the lubricating oil composition. The results are shown in Table 2. Comparative Example 7 The same paraffinic mineral oil (20cst (40°C)) used in Example 5, 94% by weight, chlorinated paraffin (Cl
Content ≒ 40% by weight) 5% by weight and Formula 6-ethyl-hexadecane-1,16 represented by
- A lubricating oil composition was obtained by blending 1% by weight of dicarboxylic acid. Grinding tests and storage stability tests were conducted on this lubricating oil composition in the same manner as in Example 6.
The results are shown in Table 2.

〔深絞り試験〕[Deep drawing test]

下記の条件で深絞りを行ない、絞り性能を評価
した。なお、ダイスのよごれは絞り比1.975で50
個絞つた後のダイスを目視観察することにより評
価した。〇はよごれなし,△はややよごれ,×は
よごれ大を示す。 深絞り条件 被加工材:JIS A1200−0,厚さ1.0mm ポンチ径:32mm クリアランス:1.5mm しわ押え力:200Kgf 加工速度:2.0m/min 比較例 8 実施例7で用いたと同じナフテン系鉱油
(56cst(40℃))99重量%および製造例3で得た反
応生成物1重量%を配合して潤滑油組成物を得、
この潤滑油組成物について実施例7と同様にして
深絞り試験,貯蔵安定性試験を行なつた。結果を
第3表に示す。 実施例 8 実施例7で用いたと同じナフテン系鉱油
(56cst(40℃))99重量%および製造例5で得た反
応生成物1重量%を配合して潤滑油組成物を得、
この潤滑油組成物について実施例7と同様にして
深絞り試験,貯蔵安定性試験を行なつた。結果を
第3表に示す。 比較例 9 実施例7で用いたと同じナフテン系鉱油
(56cst(40℃))99重量%およびオレイン酸1重量
%を配合して潤滑油組成物を得、この潤滑油組成
物について実施例7と同様にして深絞り試験,貯
蔵安定性試験を行なつた。結果を第3表に示す。 比較例 10 実施例8で用いたと同じナフテン系鉱油
(56cst(40℃))99重量%および 式 で表わされる6−エチル−ヘキサデカン−1,16
−ジカルボン酸1.0重量%配合して潤滑油組成物
を得た。この潤滑油組成物について実施例7と同
様にして深絞り試験,貯蔵安定性試験を行なつ
た。結果を第3表に示す。
Deep drawing was performed under the following conditions and the drawing performance was evaluated. In addition, the dirt on the die is 50 at an aperture ratio of 1.975.
Evaluation was made by visually observing the dice after being squeezed. ○ indicates no stain, △ indicates slight stain, and × indicates large stain. Deep drawing conditions Work material: JIS A1200-0, thickness 1.0mm Punch diameter: 32mm Clearance: 1.5mm Wrinkle holding force: 200Kgf Processing speed: 2.0m/min Comparative example 8 Same naphthenic mineral oil as used in Example 7 ( 56cst (40°C)) and 1% by weight of the reaction product obtained in Production Example 3 to obtain a lubricating oil composition,
A deep drawing test and a storage stability test were conducted on this lubricating oil composition in the same manner as in Example 7. The results are shown in Table 3. Example 8 A lubricating oil composition was obtained by blending 99% by weight of the same naphthenic mineral oil (56cst (40°C)) used in Example 7 and 1% by weight of the reaction product obtained in Production Example 5,
A deep drawing test and a storage stability test were conducted on this lubricating oil composition in the same manner as in Example 7. The results are shown in Table 3. Comparative Example 9 A lubricating oil composition was obtained by blending 99% by weight of the same naphthenic mineral oil (56cst (40°C)) used in Example 7 and 1% by weight of oleic acid. Deep drawing tests and storage stability tests were conducted in the same manner. The results are shown in Table 3. Comparative Example 10 Same naphthenic mineral oil (56cst (40℃)) as used in Example 8, 99% by weight and formula 6-ethyl-hexadecane-1,16 represented by
- A lubricating oil composition was obtained by blending 1.0% by weight of dicarboxylic acid. A deep drawing test and a storage stability test were conducted on this lubricating oil composition in the same manner as in Example 7. The results are shown in Table 3.

【表】【table】

Claims (1)

【特許請求の範囲】 1 (A) 鉱油および/または合成油及び (B) 一般式 〔式中、Xは0または1を示す。〕 または で表わされる脂肪族ジカルボン酸またはその水添
物と総炭素数20〜60の第2級または第3級のアル
キルアミンとの反応により生成する塩からなる潤
滑油組成物。 2 (B) 脂肪族ジカルボン酸とアルキルアミンと
の反応により生成する塩を0.01重量%以上の割
合で配合してなる特許請求の範囲第1項記載の
潤滑油組成物。 3 (B) 脂肪族ジカルボン酸とアルキルアミンと
の反応により生成する塩が、前者:後者=1:
0.2〜10(モル比)の割合で反応させたものであ
る特許請求の範囲第1項または第2項記載の潤
滑油組成物。
[Claims] 1 (A) Mineral oil and/or synthetic oil and (B) General formula [In the formula, X represents 0 or 1. 〕 or A lubricating oil composition comprising a salt produced by the reaction of an aliphatic dicarboxylic acid represented by the formula or its hydrogenated product with a secondary or tertiary alkylamine having a total of 20 to 60 carbon atoms. 2. The lubricating oil composition according to claim 1, which contains (B) a salt produced by the reaction of an aliphatic dicarboxylic acid and an alkylamine in a proportion of 0.01% by weight or more. 3 (B) The salt produced by the reaction of an aliphatic dicarboxylic acid and an alkylamine is the former: the latter = 1:
The lubricating oil composition according to claim 1 or 2, which is reacted at a ratio of 0.2 to 10 (molar ratio).
JP7357985A 1985-04-09 1985-04-09 Lubricating oil composition Granted JPS61233091A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP7357985A JPS61233091A (en) 1985-04-09 1985-04-09 Lubricating oil composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7357985A JPS61233091A (en) 1985-04-09 1985-04-09 Lubricating oil composition

Publications (2)

Publication Number Publication Date
JPS61233091A JPS61233091A (en) 1986-10-17
JPH0329277B2 true JPH0329277B2 (en) 1991-04-23

Family

ID=13522346

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7357985A Granted JPS61233091A (en) 1985-04-09 1985-04-09 Lubricating oil composition

Country Status (1)

Country Link
JP (1) JPS61233091A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5030502B2 (en) * 2006-08-01 2012-09-19 Jx日鉱日石エネルギー株式会社 Engine oil composition
JP7407591B2 (en) * 2019-12-26 2024-01-04 ユシロ化学工業株式会社 Oil compositions and processing fluids used for processing inorganic materials

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4986233A (en) * 1972-08-08 1974-08-19
JPS60118799A (en) * 1983-11-29 1985-06-26 Nippon Oil Co Ltd Lubricant for working metal

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4986233A (en) * 1972-08-08 1974-08-19
JPS60118799A (en) * 1983-11-29 1985-06-26 Nippon Oil Co Ltd Lubricant for working metal

Also Published As

Publication number Publication date
JPS61233091A (en) 1986-10-17

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