JPS62149794A - Lubricating oil - Google Patents
Lubricating oilInfo
- Publication number
- JPS62149794A JPS62149794A JP29647185A JP29647185A JPS62149794A JP S62149794 A JPS62149794 A JP S62149794A JP 29647185 A JP29647185 A JP 29647185A JP 29647185 A JP29647185 A JP 29647185A JP S62149794 A JPS62149794 A JP S62149794A
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- Prior art keywords
- oil
- oils
- double bond
- lubricating oil
- hydroxyl group
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Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は圧延、引抜き、伸線、切削、研削、プレス等の
金属加工の際の金属加工油等に用いられる潤滑油に関す
る。DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to a lubricating oil used as a metal working oil during metal working such as rolling, drawing, wire drawing, cutting, grinding, and pressing.
圧延油、引抜き油、伸線油、切削油、研削油、プレス油
等の金属加工油として従来より動植物油脂、鉱物油等あ
るいはこれらの混合物に必要により油性向上剤、極圧添
加剤、防錆剤、酸化防止剤、乳化剤等を添加したものを
そのまま又は1〜30%程度のエマルジョンとして用い
ており、この種金属加工油として例えば活性白土で加熱
処理した変成油脂を含有する銅層冷間圧延油(特公昭5
1−6686号)、不飽和脂肪酸の二重結合部分にオキ
シラン酸素を結合させたエポキシ化脂肪酸を水和して得
られるポリヒドロキシ脂肪酸の塩を含有する水溶性切削
油組成物(特開昭60−88096号)等が知られてい
る。Conventionally used as metal processing oils such as rolling oil, drawing oil, wire drawing oil, cutting oil, grinding oil, and press oil, oiliness improvers, extreme pressure additives, and rust preventive agents are added to animal and vegetable oils, mineral oils, etc., or mixtures thereof as necessary. It is used as it is or as an emulsion of about 1 to 30% to which additives, antioxidants, emulsifiers, etc. are added, and as this type of metal working oil, for example, copper layer cold rolling containing modified oils and fats heat-treated with activated clay. Oil (Tokuko Showa 5)
No. 1-6686), a water-soluble cutting oil composition containing a salt of a polyhydroxy fatty acid obtained by hydrating an epoxidized fatty acid in which oxirane oxygen is bonded to the double bond portion of an unsaturated fatty acid (Japanese Patent Application Laid-open No. 1-6686) -88096) etc. are known.
しかしながら特公昭51−6686号公報に記載された
変成油脂を主成分とする冷間圧延油は潤滑性には優れ、
また変成油脂は油脂に比べて親水性も改善されるものの
未だ充分なものとはいえず、エマルジョンとして用いる
場合、乳化が困難であったり、乳化安定性が低く分離を
生じ易い等の問題があった。一方特開昭60−8809
6号に記載された切削油組成物の基油として用いられて
いるポリヒドロキシ脂肪酸の塩は水溶性に優れてはいる
が、潤滑性が必ずしも充分とはいえないという問題があ
った。更に近年、加工機械の大型化、精密化、金属材料
の硬度の上昇、金属加工の高速高圧力化、製品加工面の
高精度化、経済性向上のための金属加工油使用量低減化
等、益々苛酷な加工条件が要求されているが、従来の金
属加工油はこのような苛酷な条件に対応できず、より高
性能の金属加工油の開発が望まれていた。However, the cold rolling oil mainly composed of modified oil and fat described in Japanese Patent Publication No. 51-6686 has excellent lubricity.
Furthermore, although the hydrophilicity of modified oils and fats has been improved compared to oils and fats, it is still not sufficient, and when used as an emulsion, there are problems such as difficulty in emulsification, low emulsion stability, and easy separation. Ta. On the other hand, JP-A-60-8809
Although the polyhydroxy fatty acid salt used as the base oil in the cutting oil composition described in No. 6 has excellent water solubility, there is a problem in that the lubricity is not necessarily sufficient. Furthermore, in recent years, processing machines have become larger and more precise, the hardness of metal materials has increased, metal processing has become faster and more pressurized, the precision of product processing surfaces has increased, and the amount of metal processing oil used has been reduced to improve economic efficiency. Increasingly harsh working conditions are being required, but conventional metal working oils cannot cope with such harsh conditions, and there has been a desire to develop metal working oils with higher performance.
本発明は上記の点に鑑みなされたもので、親水性、潤滑
性に優れ、そのままあるいは他の添加剤と混合して金属
加工油として用いることにより優れた加工性を発揮する
潤滑油を提供することを目的とする。The present invention has been made in view of the above points, and provides a lubricating oil that has excellent hydrophilicity and lubricity, and exhibits excellent workability when used as a metal working oil as it is or mixed with other additives. The purpose is to
本発明における第1の潤滑油は不飽和二重結合を有する
重合動植物油脂の二重結合部分に導入された水酸基を有
する化合物である。The first lubricating oil in the present invention is a compound having a hydroxyl group introduced into the double bond portion of a polymerized animal or vegetable oil or fat having an unsaturated double bond.
上記重合動植物油脂は不飽和二重結合を有する油脂を重
合せしめてなる不飽和二重結合を有する重合油である。The polymerized animal and vegetable oils and fats mentioned above are polymerized oils having unsaturated double bonds, which are obtained by polymerizing fats and oils having unsaturated double bonds.
不飽和二重結合を有する油脂としては動物油脂、植物油
脂等が挙げられ、動物油脂としては例えば牛脂、豚脂等
やイワシ油、サバ油、サンマ油、タラ油、マグロ油、イ
カ油等の魚油が用いられる。また植物油脂としてはパー
ム油、ナタネ油、大豆油、ヒマシ油等が用いられる。こ
れら油脂はニッケル系触媒を用い、圧力1.0〜4.0
kg / crA、温度160〜200℃程度で水素添
加して用いることもできるが、ヨウ素価が60以上のも
のを用いることが好ましい。またヒマシ油を脱水して不
飽和二重結合を増加せしめた脱水ヒマシ油等を用いるこ
ともできる。上記油脂は動植物から搾油して得た粗油を
用いてもよ(、粗油を燐酸、硫酸等で処理して脱ロウ等
を行い、トリグリセライド含有量を高めた予備精製油、
更にアルカリ水溶液、活性白土、活性炭等で処理し、脱
酸、脱色した精製油を用いてもよい。動植物油脂を重合
する方法としては酸化重合法、熱重合法等が挙げられ、
酸化重合法では空気または酸素を吹込みながら150〜
200℃に加熱して1〜30時間反応することにより重
合を行うことができ、熱重合法では250〜300℃に
加熱して1〜30時間程度反応することにより重合を行
うことができる。Examples of fats and oils having unsaturated double bonds include animal fats and fats, vegetable oils, etc. Examples of animal fats include beef tallow, pork fat, etc., sardine oil, mackerel oil, saury oil, cod oil, tuna oil, squid oil, etc. Fish oil is used. Further, as the vegetable oil, palm oil, rapeseed oil, soybean oil, castor oil, etc. are used. These oils and fats use a nickel-based catalyst, and the pressure is 1.0 to 4.0.
kg/crA and hydrogenated at a temperature of about 160 to 200° C., but it is preferable to use one with an iodine value of 60 or more. It is also possible to use dehydrated castor oil, which is obtained by dehydrating castor oil to increase the number of unsaturated double bonds. The above-mentioned fats and oils may be crude oils obtained by extracting oil from animals and plants (pre-refined oils with increased triglyceride content by treating crude oils with phosphoric acid, sulfuric acid, etc. to remove wax, etc.)
Furthermore, purified oil that has been treated with an aqueous alkaline solution, activated clay, activated carbon, etc. to be deoxidized and decolorized may also be used. Methods for polymerizing animal and vegetable oils include oxidative polymerization, thermal polymerization, etc.
In the oxidative polymerization method, 150 ~
Polymerization can be carried out by heating to 200°C and reacting for 1 to 30 hours, and in the thermal polymerization method, polymerization can be carried out by heating to 250 to 300°C and reacting for about 1 to 30 hours.
このようにして得られる不飽和二重結合を存する重合動
植物油脂はヨウ素価が40以上のものが好ましく、また
40℃における粘度が100〜2000センチストーク
スであることが好ましい。The thus obtained polymerized animal and vegetable oils and fats containing unsaturated double bonds preferably have an iodine value of 40 or more and a viscosity at 40° C. of 100 to 2000 centistokes.
上記重合動植物油脂の二重結合部分に水酸基を導入する
方法としては、重合動植物油脂を過酢酸、過酸化水素等
の過酸化物と反応せしめて二重結合部分をエポキシ化し
た後、該エポキシ基を水酸基とする方法が挙げられる。The method for introducing a hydroxyl group into the double bond portion of the polymerized animal or vegetable oil is to react the polymerized animal or vegetable oil with a peroxide such as peracetic acid or hydrogen peroxide to epoxidize the double bond portion, and then the epoxy group is An example of this method is to use hydroxyl as a hydroxyl group.
上記過酸化物は不飽和二重結合を有する重合動植物油脂
に対して純分で0.5〜10wt%程度を添加し、触媒
として蟻酸、燐酸、硫酸等を用いて60〜80℃で2時
間程度反応することにより重合動植物油脂の二重結合部
分にエポキシ基を導入することができる。反応終了後、
100〜120℃程度で脱水して本発明の第1の潤滑油
が得られる。エポキシ基は不安定な基であり、通常エポ
キシ化して得られた反応生成物は反応により生成する水
や水洗による精製等の工程でエポキシ基が略完全に水酸
基となるが、本発明の目的を妨げない程度であれば必ず
しもエポキシ基の全てが水酸基となっていなくてもよく
多少のエポキシ基が残存していてもよい。The above peroxide is added in a pure amount of about 0.5 to 10 wt% to polymerized animal and vegetable fats and oils having unsaturated double bonds, and heated at 60 to 80°C for 2 hours using formic acid, phosphoric acid, sulfuric acid, etc. as a catalyst. An epoxy group can be introduced into the double bond portion of the polymerized animal or vegetable oil or fat by a certain degree of reaction. After the reaction is complete,
The first lubricating oil of the present invention is obtained by dehydration at about 100 to 120°C. The epoxy group is an unstable group, and the epoxy group in the reaction product obtained by epoxidation is almost completely converted into a hydroxyl group during purification steps such as water generated by the reaction and washing with water. Not all of the epoxy groups may be hydroxyl groups, and some epoxy groups may remain as long as they do not interfere.
本発明の第2の潤滑油は不飽和二重結合を有する重合動
植物油脂の二重結合部分に水酸基を導入してなるヒドロ
キシル化重合動植物油脂(上記第1の潤滑油)の水酸基
にアルキレンオキシドを反応せしめて導入されたポリオ
キシアルキレンエーテル基を有する化合物である。アル
キレンオキシドとしてはエチレンオキシド、プロピレン
オキシド、ブチレンオキシド等が挙げられ、これらは1
種のみを付加してもよく、また2種以上をランダム付加
してもブロック付加してもよい。アルキレンオキシドは
重合動植物油脂に対して1〜10wt%付加することが
好ましい。アルキレンオキシドが付加される水酸基は通
常、不飽和二重結合を有する重合動植物油脂の二重結合
部分に導入された水酸基であるが、重合動植物油脂の原
料油脂がヒマシ油等の如く、水酸基を有する油脂である
場合、該水酸基部分にもアルキレンオキシドが付加して
ポリオキシアルキレンエーテル基が導入されてもよい。The second lubricating oil of the present invention is obtained by introducing a hydroxyl group into the double bond part of a polymerized animal or vegetable oil having an unsaturated double bond, and by introducing an alkylene oxide into the hydroxyl group of the hydroxylated polymerized animal or vegetable oil (the above-mentioned first lubricating oil). It is a compound having a polyoxyalkylene ether group introduced by reaction. Examples of alkylene oxides include ethylene oxide, propylene oxide, butylene oxide, etc.
Only seeds may be added, or two or more types may be added randomly or in blocks. The alkylene oxide is preferably added in an amount of 1 to 10 wt% based on the polymerized animal or vegetable oil. The hydroxyl group to which alkylene oxide is added is usually a hydroxyl group introduced into the double bond portion of polymerized animal and vegetable oils having unsaturated double bonds, but raw material oils and fats for polymerized animal and vegetable oils, such as castor oil, have hydroxyl groups. When it is an oil or fat, an alkylene oxide may be added to the hydroxyl group to introduce a polyoxyalkylene ether group.
前記第1の潤滑油も水酸基を有することによって親水性
に優れているが、アルキレンオキシドを付加してポリオ
キシアルキレンエーテル基とすることにより更に親水性
を高めることができる。The first lubricating oil also has excellent hydrophilicity due to having a hydroxyl group, but the hydrophilicity can be further improved by adding alkylene oxide to form a polyoxyalkylene ether group.
上記第1の潤滑油、第2の潤滑油ともに40℃における
粘度が80〜3000センチストークスであることが好
ましいが、製造工程における取扱上は100〜2000
センチストークスのものが好ましく、潤滑性能上からは
400〜3000センチストークスの粘度のものが好ま
しく、製造工程上の取扱及び潤滑性の両方を考慮すると
100〜2000センチストークスの粘度のものが好ま
しい。Both the first lubricating oil and the second lubricating oil preferably have a viscosity of 80 to 3,000 centistokes at 40°C, but the viscosity is preferably 80 to 2,000 centistokes during the manufacturing process.
A viscosity of 400 to 3,000 centistokes is preferable from the viewpoint of lubricating performance, and a viscosity of 100 to 2,000 centistokes is preferable from the viewpoint of both handling during the manufacturing process and lubricity.
本発明の潤滑油はそのままあるいは必要により動植物油
脂、脂肪酸エステル、鉱物油、極圧添加剤、酸化防止剤
、界面活性剤、防錆剤、消泡剤等と混合して圧延油、引
抜き油、伸線油、切削油、プレス油等の金属加工油に使
用される。本発明の潤滑油は親水性に優れ、乳化剤なし
若しくはきわめて少ない世の乳化剤の使用によっても容
易にエマルジョンとすることができ、エマルジョン調整
が容易に行えるとともに、エマルジョンの安定性にも優
れている。The lubricating oil of the present invention can be used as it is or, if necessary, mixed with animal and vegetable oils, fatty acid esters, mineral oil, extreme pressure additives, antioxidants, surfactants, rust preventives, antifoaming agents, etc. to produce rolling oil, drawing oil, etc. Used in metal processing oils such as wire drawing oil, cutting oil, and press oil. The lubricating oil of the present invention has excellent hydrophilicity, can be easily made into an emulsion without an emulsifier, or by using a very small amount of a conventional emulsifier, and emulsions can be easily prepared and have excellent emulsion stability.
以下、実施例を挙げて本発明を更に詳細に説明する。尚
、実施例、比較例においれ使用した原料油脂は、特に明
記したちの以外は全て粗油を用いた。Hereinafter, the present invention will be explained in more detail with reference to Examples. In addition, the raw material fats and oils used in Examples and Comparative Examples were all crude oils except where specified.
実施例1〜7
攪拌機、冷却器、温度計を取付けた31の四ツロフラス
コに第1表に示す油脂1800gを仕込み、空気を吹込
みながら180℃で2時間加熱攪拌し、同表に示す重合
油を得た。次いで80℃に冷却し、第1表に示す量の3
5%過酸化水素水及び触媒として蟻酸を全仕込量の1%
添加し80℃で2時間加熱攪拌し、反応終了後2回水洗
した後、120 ℃で脱水して得た化合物を潤滑油とし
た。Examples 1 to 7 1,800 g of the oils and fats shown in Table 1 were placed in a No. 31 four-way flask equipped with a stirrer, a cooler, and a thermometer, and heated and stirred at 180°C for 2 hours while blowing air to produce the polymerized oils shown in the table. I got it. It was then cooled to 80°C and 3
1% of the total amount of 5% hydrogen peroxide solution and formic acid as a catalyst
The mixture was heated and stirred at 80°C for 2 hours, and after the reaction was completed, the mixture was washed twice with water and dehydrated at 120°C. The resulting compound was used as a lubricating oil.
尚、実施例5〜7については更に水酸化カリウムを触媒
として用い、第1表に示すアルキレンオキシドを付加せ
しめて潤滑油とした。これらの潤滑油の性状を第2表に
示す。In Examples 5 to 7, potassium hydroxide was further used as a catalyst, and the alkylene oxides shown in Table 1 were added to prepare lubricating oils. The properties of these lubricating oils are shown in Table 2.
実施例8〜14
実施例1〜7と同様のフラスコに、第1表に示す油脂1
800gを仕込み、窒素ガス雰囲気下で300℃で3時
間加熱撹拌し、第1表に示す重合油を得た。次いで実施
例1〜7と同様にして第1表に示す量の35%過酸化水
素水を反応させ、反応終了後、水洗、脱水を行って得た
化合物を潤滑油とした。尚、実施例12〜14について
は更に水酸化カリウムを触媒として用い、第1表に示す
アルキレンオキシドを付加せしめて潤滑油とした。Examples 8 to 14 Into the same flask as in Examples 1 to 7, oil 1 shown in Table 1 was added.
800 g was charged and heated and stirred at 300° C. for 3 hours under a nitrogen gas atmosphere to obtain the polymerized oil shown in Table 1. Next, in the same manner as in Examples 1 to 7, a 35% hydrogen peroxide solution was reacted in the amount shown in Table 1. After the reaction was completed, the resulting compound was washed with water and dehydrated, and the resulting compound was used as a lubricating oil. In Examples 12 to 14, potassium hydroxide was further used as a catalyst, and the alkylene oxides shown in Table 1 were added to obtain lubricating oils.
これら潤滑油の性状を第2表に示す。The properties of these lubricating oils are shown in Table 2.
比較例1
第1表に示す魚油を実施例と同様の方法により重合して
得た重合魚油を潤滑油とした。この潤滑油(重合魚油)
の性状を第2表に示す。Comparative Example 1 A polymerized fish oil obtained by polymerizing the fish oils shown in Table 1 in the same manner as in Examples was used as a lubricating oil. This lubricating oil (polymerized fish oil)
The properties are shown in Table 2.
比較例2
第1表に示す魚油1800g、35%過酸化水素水90
g、蟻酸18gを実施例と同様のフラスコに仕込み、8
0〜90℃で2時間加熱攪拌して得たヒドロキシル化魚
油を潤滑油とした。得られた潤滑油(ヒドロキシル化魚
油)の性状を第2表に示す。Comparative Example 2 1800 g of fish oil shown in Table 1, 90 g of 35% hydrogen peroxide solution
g, 18 g of formic acid was placed in the same flask as in Example,
Hydroxylated fish oil obtained by heating and stirring at 0 to 90°C for 2 hours was used as a lubricating oil. The properties of the obtained lubricating oil (hydroxylated fish oil) are shown in Table 2.
実施例15〜19、比較例3〜4
第3表に示す配合の加工油を15%エマルジョンとして
ホモミキサー(8000rpm)で攪拌し、80℃に保
持しつつギヤポンプで循環させながらノズル(1/4
KSAOO480)より圧延鋼板(SPC−C−3B、
IX50X150mm)上に付着油量が約1.5g/m
となるようにスプレーした後、以下の条件で圧延を行っ
た。圧延前の鋼板には予め間隔50n+の2本の線を引
いておき、圧延後、2本の綿の間隔が167mm(圧下
率70%)となる時の圧延荷重をロードセルにて測定し
、圧延性能を比較した。結果を第3表に示す。Examples 15-19, Comparative Examples 3-4 A 15% emulsion of machining oil shown in Table 3 was stirred in a homomixer (8000 rpm), maintained at 80°C and circulated by a gear pump, and poured into a nozzle (1/4
KSAOO480) rolled steel plate (SPC-C-3B,
The amount of oil attached to the surface (IX50X150mm) is approximately 1.5g/m
After spraying, rolling was performed under the following conditions. Two lines with an interval of 50n+ are drawn on the steel plate before rolling, and after rolling, the rolling load when the interval between the two cotton sheets becomes 167 mm (rolling reduction rate 70%) is measured using a load cell. Performance was compared. The results are shown in Table 3.
圧延試験条件
圧延機二四段ロール式圧延機
ワークロール:径150關×幅140 mハックアップ
ロール:径250關×幅140 +uロール材質ニクロ
ム鋼
ロール周速: 30 m /min。Rolling test conditions Rolling machine Two-four-high roll type rolling mill Work roll: Diameter 150 mm x Width 140 m Hack-up roll: Diameter 250 mm x Width 140 mm + U Roll Material Nichrome steel Roll Peripheral speed: 30 m /min.
圧延材料:5PC−CSB
1 wisX 5 0mmx l 5
Qmm実施例20〜24、比較例5〜6
第4表に示す配合の加工油を切削油として用い、以下の
条件で切削した際の切削抵抗値を測定した。Rolling material: 5PC-CSB 1 wisX 5 0mmx l 5
Qmm Examples 20 to 24, Comparative Examples 5 to 6 Using the machining oil with the formulation shown in Table 4 as the cutting oil, the cutting resistance value was measured when cutting was performed under the following conditions.
また切削した表面の切削方向の粗さを触針式粗さ測定機
で測定した。結果を第4表に併せて示す。Furthermore, the roughness of the cut surface in the cutting direction was measured using a stylus type roughness measuring machine. The results are also shown in Table 4.
切削試験条件
切削機:3ton立型内面引抜きブローチ盤切削工具:
1刃当たりの切込み最大深さ0.05鰭、幅7關、刃間
隔8龍、祠質5K
855のキープローチェ具
被削材: S−45G
切削速度:2m/min。Cutting test conditions Cutting machine: 3 ton vertical internal drawing broach machine Cutting tool:
Maximum depth of cut per tooth: 0.05 fins, width: 7 teeth, blade spacing: 8 dragons, abrasion quality: 5K 855 key proche tool Work material: S-45G Cutting speed: 2 m/min.
実施例25〜28、比較例7
第5表に示す配合の加工油をアルミニウム板の両面にI
g/rrrの付着量となるように塗布し、アルミニウム
板の深絞り加工試験を以下の条件で行い、種々の絞り比
による絞り加工の際の絞り荷重を測定した。結果を第5
表に示す。Examples 25 to 28, Comparative Example 7 Processing oil with the composition shown in Table 5 was applied to both sides of an aluminum plate.
A deep drawing test was conducted on an aluminum plate under the following conditions, and the drawing load during drawing at various drawing ratios was measured. 5th result
Shown in the table.
深絞り加工試験条件
試験機:高速深絞り加工試験機(東京試験機(株製)、
ポンチ径32mm、ダイス径35龍、加工速度1m/s
ec。Deep drawing test conditions Test machine: High speed deep drawing test machine (manufactured by Tokyo Test Instruments Co., Ltd.)
Punch diameter 32mm, die diameter 35mm, processing speed 1m/s
ec.
加工材:厚さl mmのアルミニウム円盤(JISAl
loo、0>、各試料油毎に径6
’1.4 mlから径66.4 mmまで0.8 wず
つ径が増加する6枚の円盤の加工を行い、絞り比1.9
5から絞り比2.075までの試験を行った。Processing material: Aluminum disk with a thickness of 1 mm (JISAl
loo, 0>, for each sample oil, we processed six disks whose diameter increased by 0.8 w from diameter 6'1.4 ml to diameter 66.4 mm, and the drawing ratio was 1.9.
5 to 2.075.
第2表
第3表
※1 キャノンフェンスケ粘度計により測定した40℃
における粘度
※2 原料の重量に対するアルキレンオキシドの添加重
量の比率
※3 製造直後と、室温で30日間放置後の臭気を以下
の基準により判定した。Table 2 Table 3 *1 40℃ measured by Cannon Fenske viscometer
Viscosity at *2 Ratio of the weight of alkylene oxide added to the weight of the raw material *3 The odor immediately after production and after being left at room temperature for 30 days was judged according to the following criteria.
動植物臭、魚臭がない・・・・・O
動植物具、魚臭ややある・・・・△
動植物臭、魚臭等が激しい・・・×
※4 試料30重量部を60−スピンドル油70重量部
と混合し、この混合物を0℃で7日間放置した後、分離
の状態を観察し以下の基準で判定した。No animal or plant odor, no fish odor...O Animal and plant utensils, fishy odor...△ Severe animal or plant odor, fish odor, etc....X *4 30 parts by weight of the sample is mixed with 60 parts by weight and 70 parts by weight of spindle oil After the mixture was left at 0° C. for 7 days, the state of separation was observed and judged according to the following criteria.
分離なし・・・・・・・・・・・○
やや分離または下部に
やや沈澱あり・・・・△
二層に分離・・・・・・・・・・×
※5 シェル式高速四球型摩擦試験機により、試験鋼球
172インチ、測定温度50℃、室軸回転数60Orp
mの条件で測定した。No separation・・・・・・・・・○ Slight separation or slight precipitation at the bottom・・・△ Separation into two layers・・・・・・・・・× ※5 Shell type high speed four-ball friction Using a testing machine, the test steel ball was 172 inches, the measurement temperature was 50℃, and the chamber shaft rotation speed was 60Orp.
It was measured under the conditions of m.
※6 ポリオキシアルキレンノニルフェニルエーテル系
非イオン界面活性剤
※7 乳化剤及び防錆剤
〔発明の効果〕
以上説明したように本発明の第1の潤滑油は不飽和二重
結合を有する重合動植物油脂の二重結合部分に水酸基が
導入された構造を有することによって、潤滑性、親水性
、安定性に優れるとともに、魚油等の粗油を原料として
用いた場合でも臭気が殆どないため安価な粗油を用いて
製造がすることができ、優れた潤滑油が安価に提供され
得る。また本発明の第2の潤滑油は上記第1の水酸基部
分にアルキレンオキシドを付加せしめてポリオキシアル
キレンエーテル基を導入した構造を有するため、第1の
潤滑油の優れた性能を有するとともに、更に親水性に優
れたものである。*6 Polyoxyalkylene nonyl phenyl ether type nonionic surfactant *7 Emulsifier and rust preventive agent [Effects of the invention] As explained above, the first lubricating oil of the present invention is a polymerized animal or vegetable oil having an unsaturated double bond. Because of its structure in which a hydroxyl group is introduced into the double bond of the oil, it has excellent lubricity, hydrophilicity, and stability, and even when crude oil such as fish oil is used as a raw material, there is almost no odor, making it an inexpensive crude oil. The lubricating oil can be produced at low cost. Furthermore, since the second lubricating oil of the present invention has a structure in which alkylene oxide is added to the first hydroxyl group to introduce a polyoxyalkylene ether group, it has the excellent performance of the first lubricating oil, and furthermore, It has excellent hydrophilicity.
本発明の潤滑油はそのまま又は動植物油脂、鉱物油脂や
他の添加剤とともに混合して圧延油、引抜き油、伸線油
、切削油、研削油、プレス油等の金属加工油として用い
られ、本発明の潤滑油を用いた金属加工油は優れた加工
性を示す等の種々の効果を有するThe lubricating oil of the present invention can be used as a metalworking oil such as rolling oil, drawing oil, wire drawing oil, cutting oil, grinding oil, press oil, etc. as it is or mixed with animal and vegetable oils, mineral oils and fats, and other additives. Metalworking oil using the lubricating oil of the invention has various effects such as excellent workability.
Claims (4)
合部分に導入された水酸基を有することを特徴とする潤
滑油。(1) A lubricating oil characterized by having a hydroxyl group introduced into the double bond portion of a polymerized animal or vegetable oil or fat having an unsaturated double bond.
ークスである特許請求の範囲第1項記載の潤滑油。(2) The lubricating oil according to claim 1, which has a viscosity of 80 to 3000 centistokes at 40°C.
合部分に水酸基を導入してなるヒドロキシル化重合動植
物油脂の水酸基にアルキレンオキシドを反応せしめて導
入されたポリオキシアルキレンエーテル基を有すること
を特徴とする潤滑油。(3) Having a polyoxyalkylene ether group introduced by reacting an alkylene oxide with the hydroxyl group of the hydroxylated polymerized animal and vegetable oil, which is obtained by introducing a hydroxyl group into the double bond portion of the polymerized animal and vegetable oil having unsaturated double bonds. A lubricating oil featuring:
ークスである特許請求の範囲第3項記載の潤滑油。(4) The lubricating oil according to claim 3, which has a viscosity of 80 to 3000 centistokes at 40°C.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60296471A JPH066712B2 (en) | 1985-12-24 | 1985-12-24 | Lubricant |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60296471A JPH066712B2 (en) | 1985-12-24 | 1985-12-24 | Lubricant |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS62149794A true JPS62149794A (en) | 1987-07-03 |
JPH066712B2 JPH066712B2 (en) | 1994-01-26 |
Family
ID=17833981
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP60296471A Expired - Lifetime JPH066712B2 (en) | 1985-12-24 | 1985-12-24 | Lubricant |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH066712B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0320833A2 (en) * | 1987-12-14 | 1989-06-21 | Klüber Chemie Kg | Aqueous release agent for producing moulded polyurethane articles |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102009019698B4 (en) * | 2009-05-05 | 2012-02-23 | Rhein-Chemie Rheinau Gmbh | Use of lubricating performance additives as lubricants for metalworking or as lubricants for machines |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS56109296A (en) * | 1980-02-02 | 1981-08-29 | Miyoshi Oil & Fat Co Ltd | Metal rolling oil |
-
1985
- 1985-12-24 JP JP60296471A patent/JPH066712B2/en not_active Expired - Lifetime
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS56109296A (en) * | 1980-02-02 | 1981-08-29 | Miyoshi Oil & Fat Co Ltd | Metal rolling oil |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0320833A2 (en) * | 1987-12-14 | 1989-06-21 | Klüber Chemie Kg | Aqueous release agent for producing moulded polyurethane articles |
Also Published As
Publication number | Publication date |
---|---|
JPH066712B2 (en) | 1994-01-26 |
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