JPH04202298A - Water soluble cutting oil - Google Patents

Water soluble cutting oil

Info

Publication number
JPH04202298A
JPH04202298A JP33132590A JP33132590A JPH04202298A JP H04202298 A JPH04202298 A JP H04202298A JP 33132590 A JP33132590 A JP 33132590A JP 33132590 A JP33132590 A JP 33132590A JP H04202298 A JPH04202298 A JP H04202298A
Authority
JP
Japan
Prior art keywords
fatty acid
acid
fatty acids
water
condensed
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
JP33132590A
Other languages
Japanese (ja)
Other versions
JP3006878B2 (en
Inventor
Masaki Kawashima
正毅 川島
Shuji Tanaka
田中 秀志
Morio Ninomiya
二宮 守男
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.)
Miyoshi Yushi KK
Miyoshi Oil and Fat Co Ltd
Original Assignee
Miyoshi Yushi KK
Miyoshi Oil and Fat 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 Miyoshi Yushi KK, Miyoshi Oil and Fat Co Ltd filed Critical Miyoshi Yushi KK
Priority to JP33132590A priority Critical patent/JP3006878B2/en
Publication of JPH04202298A publication Critical patent/JPH04202298A/en
Application granted granted Critical
Publication of JP3006878B2 publication Critical patent/JP3006878B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Landscapes

  • Lubricants (AREA)

Abstract

PURPOSE:To provide the title oil improved in the prevention of foaming, rust proofness and storage stability by using an alkali metal salt and/or amine salt of a specific condensed fatty acid. CONSTITUTION:A condensed fatty acid with an acid value of 55-130 is prepared by subjecting a monohydroxy fatty acid (e.g. 12-hydroxy-9-octadecenoic acid) or a mixture thereof with 60wt.% or less of a dihydroxy fatty acid to a dehydration condensation at 100-200 deg.C for 30min to 8hr in an inert gas atmosphere. The condensed fatty acid is neutralized with an alkali metal hydroxide (e.g. NaOH) or an amine compound (e.g. ammonia) to obtain an alkali metal salt or amine salt of the condensed fatty acid. The title cutting oil is prepared by dissolving 0.1-50wt.% of the obtained salt in water.

Description

【発明の詳細な説明】 [産業上の利用分野] 本発明は水溶性切削油剤に関する。さらに詳しくは、低
起泡性で防錆性に優れ、切削、研削等の金属加工に用い
る水溶性切削油剤に関する。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a water-soluble cutting fluid. More specifically, the present invention relates to a water-soluble cutting fluid that has low foaming properties and excellent rust prevention properties and is used in metal processing such as cutting and grinding.

[従来の技術] 従来、切削、研削等の金属加工には、切削性能、研削性
能に優れ、冷却効率の良い水溶性切削油剤が広く用いら
れている。これらの水溶性切削油剤はナフテン酸、ロジ
ン酸、脂肪酸等のアルカリ金属塩又はアミン塩等を主成
分とするもので、−船釣に発泡し易く、特に脂肪酸のア
ルカリ金属塩は発泡し易く、生成する泡のために作業性
が低下し、また加工材に錆や腐食を発生させる欠点があ
った。
[Prior Art] Conventionally, water-soluble cutting fluids have been widely used for metal processing such as cutting and grinding, as they have excellent cutting performance and grinding performance, and have good cooling efficiency. These water-soluble cutting fluids are mainly composed of alkali metal salts or amine salts of naphthenic acids, rosin acids, fatty acids, etc. - They tend to foam during boat fishing, especially alkali metal salts of fatty acids. The workability is reduced due to the bubbles produced, and there is also the disadvantage that the processed materials may become rusty or corroded.

この様な欠点を改良し、低起泡性で、防錆性のある水溶
性切削油剤が報告されている。
Water-soluble cutting fluids have been reported that improve these drawbacks and have low foaming and rust prevention properties.

例えば、エポキシ化脂肪酸またはこれを水和して得られ
るポリヒドロキシル化脂肪酸の塩を用いる水溶性切削油
剤(特開昭60−88096号)、リシノール酸重縮合
物のアルカリ金属塩、またはアミン塩を用いる水溶性切
削油剤(特公平2−5799号)等が知られている。
For example, water-soluble cutting fluids using epoxidized fatty acids or salts of polyhydroxylated fatty acids obtained by hydrating them (Japanese Patent Application Laid-open No. 88096/1983), alkali metal salts of ricinoleic acid polycondensates, or amine salts. Water-soluble cutting fluids (Japanese Patent Publication No. 2-5799) and the like are known.

[発明が解決しようとする問題点コ しかしながら従来知られているこれらの水溶性切削油剤
は、切削、研削に用いて十分な効果を発揮していない。
[Problems to be Solved by the Invention] However, these conventionally known water-soluble cutting fluids do not exhibit sufficient effects when used in cutting and grinding.

例えば、エポキシ化脂肪酸を用いるものは、水溶液の状
態で長期に使用するとエポキシ基が徐々に水和されてヒ
ドロキシル基となって、経時安定性が低く、またポリヒ
ドロキシル化脂肪酸の塩を用いるものは、水溶性に優れ
るものの、切削時の潤滑性が十分てないという問題点が
あった。またリシノール酸重合物のアルカリ金属塩、ま
たはアミン塩を用いる方法では、分子中に二重結合を多
量に含み使用中に重合を起こすために、溶液が不安定で
、分離したり、金属の表面にスラッジが発生したり、も
しくは粘度が上昇する等の欠点があった。
For example, when using epoxidized fatty acids for a long period of time in an aqueous solution state, the epoxy groups gradually become hydrated and become hydroxyl groups, resulting in low stability over time, and those using polyhydroxylated fatty acid salts Although it has excellent water solubility, it has the problem of insufficient lubricity during cutting. In addition, methods using alkali metal salts or amine salts of ricinoleic acid polymers contain a large amount of double bonds in the molecule and polymerize during use, making the solution unstable and causing problems such as separation and metal surfaces. However, there were disadvantages such as generation of sludge or increase in viscosity.

本発明は上記課題に着目し行ったもので、水溶性切削油
剤として用いた時に、優れた切削性能、研削性能を発揮
すると共に、防錆性、保存安定性に優れ、かつ低起泡性
である水溶性切削油材を提供することを目的とする。
The present invention was developed in view of the above-mentioned problems, and when used as a water-soluble cutting fluid, it exhibits excellent cutting performance and grinding performance, has excellent rust prevention properties, storage stability, and has low foaming properties. The purpose of the present invention is to provide a certain water-soluble cutting fluid.

[問題点を解決するための手段] 本発明者等は、上記課題を解決するため鋭意研究を行っ
た結果、ヒドロキシ化合物の重縮合物であって、かつ側
鎖にヒドロキシル基を有する特定の化合物を水溶性切削
油剤として用いることにより、優れた切削性能、研削性
能を有すると共に、防錆性、保存安定性に優れ、かつ低
起泡性である水溶性切削油剤を見出し本発明を完成する
に至った。
[Means for Solving the Problems] As a result of intensive research to solve the above problems, the present inventors have developed a specific compound that is a polycondensate of hydroxy compounds and has a hydroxyl group in its side chain. In order to complete the present invention, we have found a water-soluble cutting fluid that has excellent cutting performance and grinding performance, has excellent rust prevention properties, excellent storage stability, and has low foaming properties by using it as a water-soluble cutting fluid. It's arrived.

即ち、本発明の要旨の一つは、ジヒドロキシ脂肪酸を脱
水縮合して得られる縮合脂肪酸のアルカリ金属塩及び又
はアミン塩を用いる水溶性切削油剤であり、さらにいま
一つの要旨はジヒドロキシ脂肪酸とモノヒドロキシ脂肪
酸とを各々あるいは混合して脱水縮合して得られる縮合
脂肪酸のアルカリ金属塩及び又はアミン塩を用いる水溶
性切削油剤である。
That is, one of the gist of the present invention is a water-soluble cutting fluid that uses an alkali metal salt and/or amine salt of a condensed fatty acid obtained by dehydration condensation of a dihydroxy fatty acid, and another gist is a water-soluble cutting fluid that uses a dihydroxy fatty acid and a monohydroxy fatty acid. This is a water-soluble cutting fluid that uses alkali metal salts and/or amine salts of condensed fatty acids obtained by dehydration condensation of these fatty acids individually or in combination.

本発明に用いるモノヒドロキシ脂肪酸としては、植物油
、ろう等を常法により加水分解し、精製して得られるモ
ノヒドロキシ脂肪酸が、またジヒドロキシ脂肪酸として
は不飽和脂肪酸から得られるジヒドロキシ脂肪酸等が挙
げられる。前者のモノヒドロキシ脂肪酸としては、ヒマ
シ油から得られる12−ヒドロキシ−9−オクタデセン
酸が挙げられ、後者のジヒドロキシ脂肪酸としては、不
飽和脂肪酸を原料とし、その不飽和結合にヒドロキシル
基を導入して得られるジヒドロキシ脂肪酸が挙げられる
Examples of monohydroxy fatty acids used in the present invention include monohydroxy fatty acids obtained by hydrolyzing and refining vegetable oils, waxes, etc. by conventional methods, and examples of dihydroxy fatty acids include dihydroxy fatty acids obtained from unsaturated fatty acids. The former monohydroxy fatty acid includes 12-hydroxy-9-octadecenoic acid obtained from castor oil, and the latter dihydroxy fatty acid is produced by using unsaturated fatty acids as raw materials and introducing hydroxyl groups into their unsaturated bonds. Dihydroxy fatty acids obtained are mentioned.

不飽和脂肪酸にヒドロキシル基を導入する方法としては
、不飽和脂肪酸に過酢酸、過酸化水素等の過酸化物を反
応し、その不飽和結合部分をエポキシ化し、ついて該エ
ポキシ基を加水分解してヒ)・0キシル基を導入する方
法が挙げられる。
A method for introducing a hydroxyl group into an unsaturated fatty acid is to react the unsaturated fatty acid with a peroxide such as peracetic acid or hydrogen peroxide, epoxidize the unsaturated bond, and then hydrolyze the epoxy group. h) A method of introducing a 0xyl group can be mentioned.

上記反応として、不飽和脂肪酸に純分てその0.2〜0
.5重量%の過酸化物を添加し、蟻酸、燐酸、硫酸等の
触媒の存在下、40〜80℃で1〜5時間反応する例が
挙げられ、この反応により不飽和脂肪酸の不飽和結合部
分がエポキシ化され、ついてエポキシ基が水和されてヒ
ドロキシ基となる。
As the above reaction, the pure content of unsaturated fatty acids is 0.2 to 0.
.. Examples include adding 5% by weight of peroxide and reacting at 40 to 80°C for 1 to 5 hours in the presence of a catalyst such as formic acid, phosphoric acid, or sulfuric acid. is epoxidized, and the epoxy group is then hydrated to become a hydroxy group.

反応終了後、反応混合物から触媒、過剰の過酸化物を水
洗して除去し、50〜120℃程度で脱水してジヒドロ
キシ脂肪酸が得られる。ここに用いる不飽和脂肪酸とし
ては、ラウロレイン酸、ミリストしイン酸、シーマリン
酸、オレイン酸、エライジン酸、リノール酸、リルイン
酸、リシノール酸、アラキドン酸、エイコサペンタエン
酸、エルカ酸等が挙げられ、これらの不飽和脂肪酸は、
単独もしくは2種以上を混合して用いることができる。
After the reaction is completed, the catalyst and excess peroxide are removed from the reaction mixture by washing with water, and the mixture is dehydrated at about 50 to 120°C to obtain dihydroxy fatty acids. Examples of the unsaturated fatty acids used here include lauroleic acid, myristioic acid, seamarinic acid, oleic acid, elaidic acid, linoleic acid, liluic acid, ricinoleic acid, arachidonic acid, eicosapentaenoic acid, erucic acid, etc. The unsaturated fatty acids are
They can be used alone or in combination of two or more.

また上記不飽和脂肪酸として、大豆油、オリーブ油、ト
ール油、ラード、チキン油、ヒマシ油、綿実油、糠油、
ナタネ油、魚油等の動植物油を常法に従い、分解後濃縮
して得られる脂肪酸を用いることができ、該油脂の脂肪
酸中に不飽和脂肪酸を少なくとも80重量%含有するこ
とが好ましい。
In addition, the unsaturated fatty acids mentioned above include soybean oil, olive oil, tall oil, lard, chicken oil, castor oil, cottonseed oil, bran oil,
Fatty acids obtained by decomposing and concentrating animal and vegetable oils such as rapeseed oil and fish oil according to a conventional method can be used, and it is preferable that the fatty acids of the oils and fats contain at least 80% by weight of unsaturated fatty acids.

本発明に用いる縮合脂肪酸は、前記ジヒドロキシ脂肪酸
もしくはモノヒドロキシ脂肪酸またはモノ及ジヒドロキ
シ脂肪酸の混合脂肪酸を用い、常法に従い脱水縮合を行
って得られる。脱水縮合はジヒドロキシ脂肪酸、モノヒ
ドロキシ脂肪酸、またはジヒドロキシ脂肪酸とモノヒド
ロキシ脂肪酸の混合脂肪酸を、窒素ガス等の不活性ガス
の気流下、100〜200℃で30分〜8時間反応する
ことにより行うことができる。
The condensed fatty acid used in the present invention is obtained by dehydration condensation using the dihydroxy fatty acid, monohydroxy fatty acid, or mixed fatty acid of mono- and dihydroxy fatty acid according to a conventional method. Dehydration condensation can be carried out by reacting dihydroxy fatty acids, monohydroxy fatty acids, or mixed fatty acids of dihydroxy fatty acids and monohydroxy fatty acids at 100 to 200°C for 30 minutes to 8 hours under a stream of inert gas such as nitrogen gas. can.

縮合反応において、得られる縮合脂肪酸の縮合度が高く
なるに従い酸価が低下するが、縮合度と酸価は逆比例関
係にあるため、酸価により縮合度を規定することができ
る。本発明ここ用いる縮合脂肪酸は55〜130の酸価
のものが好ましい。酸価が55未満の縮合脂肪酸は、水
溶性が低いとともに粘度が高く、扱いにくいものどなり
、また酸価が130を越える縮合脂肪酸は、その塩の水
溶性は良いものの、スカムが発生し易いものとなり好ま
しくない。
In the condensation reaction, as the degree of condensation of the resulting condensed fatty acid increases, the acid value decreases; however, since the degree of condensation and the acid value are in an inversely proportional relationship, the degree of condensation can be determined by the acid value. The condensed fatty acids used in the present invention preferably have an acid value of 55 to 130. Condensed fatty acids with an acid value of less than 55 have low water solubility and high viscosity, making them difficult to handle, and condensed fatty acids with an acid value of over 130 have good water solubility, but tend to form scum. This is undesirable.

また上記縮合脂肪酸はジヒドロキシ脂肪酸分子中のヒド
ロキシル基とカルボシキル基とが縮合したエステル基を
介した高分子化した化合物であり、その末端にカルボキ
シル基を有するとともに、側鎖にヒドロキシル基を有す
ることに特徴があり、そのため通常の高分子化合物より
も水溶性に優れる。さらに側鎖のヒドロキシル基の量は
ジヒドロキシ脂肪酸にモノヒドロキシ脂肪酸を併用する
ことにより加減することができ、これにより水溶性を調
整することができる。モノヒドロキシ脂肪酸を併用する
場合、ジヒドロキシ脂肪酸に対しモノヒドロキシ脂肪酸
の添加量は60重量%以下が好ましい。モノヒドロキシ
脂肪酸の添加量が60重量%を越えると安定性が低下す
る。すなわち、モノヒドロキシ脂肪酸は分子中に不飽和
結合を有し・、これが多量になると使用中に熱重合を起
こし、粘度の上昇、あるいは水溶性の低下、スカムの発
生が生し易くなる。
In addition, the condensed fatty acids mentioned above are polymerized compounds through ester groups in which hydroxyl groups and carboxyl groups in dihydroxy fatty acid molecules are condensed, and have a carboxyl group at the end and a hydroxyl group in the side chain. Because of these characteristics, it has better water solubility than ordinary polymer compounds. Furthermore, the amount of hydroxyl groups in the side chain can be adjusted by using monohydroxy fatty acid in combination with dihydroxy fatty acid, thereby adjusting the water solubility. When monohydroxy fatty acids are used together, the amount of monohydroxy fatty acids added is preferably 60% by weight or less based on the dihydroxy fatty acids. If the amount of monohydroxy fatty acid added exceeds 60% by weight, stability decreases. That is, monohydroxy fatty acids have unsaturated bonds in their molecules, and when they are present in large quantities, they undergo thermal polymerization during use, resulting in increased viscosity, decreased water solubility, and scum formation.

次に上記縮合脂肪酸を常法に従い、アルカリ金属の水酸
化物及び又はアミン化合物で中和することにより、本発
明に用いる縮合脂肪酸のアルカリ金属塩及び又はアミン
塩が得られる。ここに用いるアルカリ金属の水酸化物と
しては、水酸化ナトリウム、水酸化カリウム等が、また
アミン化合物としてはアンモニア、トリエチルアミン、
モノエタノールアミン、ジェタノールアミン、トリエタ
ノールアミン等が挙げられる。
Next, the alkali metal salt and/or amine salt of the condensed fatty acid used in the present invention is obtained by neutralizing the condensed fatty acid with an alkali metal hydroxide and/or amine compound according to a conventional method. The alkali metal hydroxides used here include sodium hydroxide, potassium hydroxide, etc., and the amine compounds include ammonia, triethylamine,
Examples include monoethanolamine, jetanolamine, triethanolamine, and the like.

上記縮合脂肪酸のアルカリ金属塩及び又はアミン塩は、
親水性に優れ、そのままもしくは極めて少ない量の乳化
剤を併用して、容易に水溶液あるいは乳化液とすること
ができ、水溶液の安定性も優れている。
The alkali metal salt and/or amine salt of the condensed fatty acid is
It has excellent hydrophilicity and can be easily made into an aqueous solution or emulsion either as it is or in combination with a very small amount of an emulsifier, and the stability of the aqueous solution is also excellent.

本発明の水溶性切削油剤は、上記縮合脂肪酸のアルカリ
金属塩及び又はアミン塩を、水溶液もしくは乳化液とし
、そのままあるいは必要によりこれに動植物油脂、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、消泡剤等を併用して切削、研削等の金属
加工に使用することができる。水溶液または他の組成物
と混合して用いる場合の縮合脂肪酸塩の濃度は0.1〜
50重量%が好ましい。
The water-soluble cutting fluid of the present invention contains the alkali metal salt and/or amine salt of the condensed fatty acid as an aqueous solution or emulsion, and can be used as it is or optionally added with animal and vegetable oils, fatty acid esters, mineral oil, extreme pressure additives, and antioxidants. It can be used in metal processing such as cutting and grinding in combination with a surfactant, a rust preventive agent, an antifoaming agent, etc. The concentration of the condensed fatty acid salt when used in an aqueous solution or mixed with other compositions is 0.1 to
50% by weight is preferred.

以下、実施例を挙げて本発明をさらに詳しく説明するが
、その要旨を越えない限り本発明はこれらに限定される
ものではない。
Hereinafter, the present invention will be explained in more detail with reference to Examples, but the present invention is not limited thereto unless the gist thereof is exceeded.

[実施例] ・ヒドロキシ化脂肪酸の調製 撹拌機、冷却器、温度計、滴下ロートを備えた四ツ目フ
ラスコに、表1に示す不飽和脂肪酸を100g及び全仕
込量の2%の蟻酸を仕込み、脂肪酸に対し35%濃度の
過酸化水素水を用い、過酸化水素1.2倍モル滴下し、
70℃で4時間加熱撹拌した。反応終了後、1回当たり
30mAの純水を用いて、反応混合物を2回水洗し、次
いで120°Cて脱水し・てヒドロキシ化脂肪酸(NO
,1〜3)を得た。得られたヒドロキシ化脂肪酸の酸価
(AV)、ヨウ素価(IV)、水酸基価(OH〜′)を
表1に示す。
[Example] - Preparation of hydroxylated fatty acids Into a four-eye flask equipped with a stirrer, a cooler, a thermometer, and a dropping funnel, 100 g of the unsaturated fatty acids shown in Table 1 and 2% of the total amount of formic acid were charged. , using a hydrogen peroxide solution with a concentration of 35% relative to the fatty acid, dropping 1.2 times the mole of hydrogen peroxide,
The mixture was heated and stirred at 70°C for 4 hours. After the reaction, the reaction mixture was washed twice with pure water at 30 mA each time, and then dehydrated at 120°C to obtain hydroxylated fatty acids (NO
, 1-3) were obtained. Table 1 shows the acid value (AV), iodine value (IV), and hydroxyl value (OH~') of the obtained hydroxylated fatty acid.

表1 ・縮合脂肪酸の調製 表1のヒドロキシ化脂肪酸、リシノール酸、12−ヒド
ロキシステアリン酸とを用い、窒素気流下、200℃で
所定時間加熱し、縮合反応を行って実施例、比較例に用
いる縮合脂肪酸を得た。
Table 1 ・Preparation of condensed fatty acids Using the hydroxylated fatty acids, ricinoleic acid, and 12-hydroxystearic acid in Table 1, heat at 200°C for a predetermined time under a nitrogen stream to perform a condensation reaction and use it in Examples and Comparative Examples. A condensed fatty acid was obtained.

得られた縮合脂肪酸の酸価、水酸基価を表2に示す。Table 2 shows the acid value and hydroxyl value of the obtained condensed fatty acids.

表2 実施例1〜7、比較例1〜4 表2に示す縮合脂肪#N0.1〜8をトリエタノールア
ミンで中和し、5%水溶液として水溶性切削油剤を調製
した。得られた水溶性切削油剤を用いて耐荷重能試験、
消泡性試験及び防錆試験を行った。各々得られた結果を
表3に、各試験方法表3 を以下に示す。
Table 2 Examples 1 to 7, Comparative Examples 1 to 4 Condensed fats #N0.1 to 8 shown in Table 2 were neutralized with triethanolamine to prepare a water-soluble cutting fluid as a 5% aqueous solution. Using the obtained water-soluble cutting fluid, a load-bearing capacity test was carried out.
A defoaming test and a rust prevention test were conducted. The results obtained are shown in Table 3, and Table 3 of each test method is shown below.

・耐荷重能試験 J I S−に−2519に準拠し、四球式摩擦試験機
により、回転数600rpmで耐荷重能を測定した。
- Load-bearing ability test The load-bearing ability was measured at a rotational speed of 600 rpm using a four-ball friction tester in accordance with JIS-2519.

・消泡性試験 水道水で60倍に希釈した水溶性切削油剤50mflを
100mρ容の共栓付メスシリンダーに入れ、密栓後、
液温30℃てメスシリンダーを上下に30回振盪し、そ
の後静置して、0秒、30秒、60秒間経過後の泡の容
積(m Il、 )を測定した。
・Anti-foaming test Pour 50 mfl of water-soluble cutting fluid diluted 60 times with tap water into a 100 mρ measuring cylinder with a stopper, and after sealing,
The measuring cylinder was shaken up and down 30 times at a liquid temperature of 30° C., then left to stand, and the foam volume (m Il, ) was measured after 0 seconds, 30 seconds, and 60 seconds.

・防錆試験 純水で希釈した1100pp濃度の水溶性切削油剤の水
溶液に、J l5−G−3141に準拠して調製したテ
ストピースを浸漬し、錆の発生量(%)を測定した。
- Rust prevention test A test piece prepared in accordance with J15-G-3141 was immersed in an aqueous solution of a water-soluble cutting fluid with a concentration of 1100 pp diluted with pure water, and the amount (%) of rust generated was measured.

実施例8〜9、比較例5 表2に示す縮合脂肪酸のトリエタノールアミン塩を表4
に示す組成に配合して水溶性切削油剤を調製し、これを
用いて以下に示す切削試験を行い切削性能(切削抵抗値
)を評価した。その結果を表4に示す。
Examples 8 to 9, Comparative Example 5 Table 4 shows triethanolamine salts of condensed fatty acids shown in Table 2.
A water-soluble cutting fluid was prepared by blending it into the composition shown below, and the cutting test shown below was conducted using this to evaluate the cutting performance (cutting resistance value). The results are shown in Table 4.

・切削試験条件 切削11:3ton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0.05m m 、幅7
mm、刃間隔8 m m 、材質5KH55のキープロ
ーチエ具 被削剤 : S−45C 切削速度:2m/min 表4 [発明の効果コ 以上説明したように、本発明は特定のヒドロキシ脂肪酸
を脱水縮合して得られる縮合脂肪酸のアルカリ金属塩及
び又はアミン塩を用いるもので、ヒドロキシ脂肪酸にジ
ヒドロキシ脂肪酸又はジヒドロキシ脂肪酸とモノヒドロ
キシ脂肪酸を用いることにより、末端にカルボキシル基
を、側鎖にヒドロキシル基を有する縮合脂肪酸となり、
その塩を用いた水溶性切削油剤は、従来の水溶性切削油
剤と比べて、切削性、研削性に優れると共に、防錆性が
良く被削物に錆を発生させることが無く、また低起泡性
で作業性に優れる等の効果を特徴する 特許出願人 ミヨシ油脂株式会社
・Cutting test conditions Cutting 11: 3 ton vertical internal drawing broach machine Cutting tool: Maximum depth of cut per tooth 0.05 mm, width 7
mm, blade spacing 8 mm, material 5KH55 key approach tool Work material: S-45C Cutting speed: 2 m/min Table 4 [Effects of the Invention] As explained above, the present invention has been developed by dehydrating and condensing specific hydroxy fatty acids. This method uses an alkali metal salt and/or amine salt of a condensed fatty acid obtained by using a dihydroxy fatty acid or a dihydroxy fatty acid and a monohydroxy fatty acid to produce a condensed fatty acid with a carboxyl group at the end and a hydroxyl group in the side chain. Then,
Compared to conventional water-soluble cutting fluids, water-soluble cutting fluids using this salt have excellent cutting and grinding properties, have good rust prevention properties, do not cause rust on the workpiece, and have low corrosion resistance. Miyoshi Oil & Fat Co., Ltd. Patent applicant for features such as foaming properties and excellent workability

Claims (1)

【特許請求の範囲】 1、ジヒドロキシ脂肪酸を脱水縮合して得られる縮合脂
肪酸のアルカリ金属塩及び又はアミン塩を用いることを
特徴とする水溶性切削油剤。 2、ジヒドロキシ脂肪酸とモノヒドロキシ脂肪酸とを各
々あるいは混合して脱水縮合して得られる縮合脂肪酸の
アルカリ金属塩及び又はアミン塩を用いることを特徴と
する水溶性切削油剤。
[Scope of Claims] 1. A water-soluble cutting fluid characterized by using an alkali metal salt and/or amine salt of a condensed fatty acid obtained by dehydration condensation of a dihydroxy fatty acid. 2. A water-soluble cutting fluid characterized by using an alkali metal salt and/or amine salt of a condensed fatty acid obtained by dehydration condensation of dihydroxy fatty acids and monohydroxy fatty acids individually or in combination.
JP33132590A 1990-11-29 1990-11-29 Water-soluble cutting fluid Expired - Fee Related JP3006878B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP33132590A JP3006878B2 (en) 1990-11-29 1990-11-29 Water-soluble cutting fluid

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP33132590A JP3006878B2 (en) 1990-11-29 1990-11-29 Water-soluble cutting fluid

Publications (2)

Publication Number Publication Date
JPH04202298A true JPH04202298A (en) 1992-07-23
JP3006878B2 JP3006878B2 (en) 2000-02-07

Family

ID=18242424

Family Applications (1)

Application Number Title Priority Date Filing Date
JP33132590A Expired - Fee Related JP3006878B2 (en) 1990-11-29 1990-11-29 Water-soluble cutting fluid

Country Status (1)

Country Link
JP (1) JP3006878B2 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0797590A (en) * 1993-09-28 1995-04-11 Nisshin Fine Chem Kk Water-soluble machining and grinding oil
WO2011052637A1 (en) * 2009-10-27 2011-05-05 国立大学法人 鹿児島大学 Nanoparticle surface modifying agent, metal nanoparticle, and method of manufacturing nanoparticle surface modifying agent
US9029306B2 (en) 2009-11-30 2015-05-12 Idemitsu Kosan., Ltd. Water-soluble metalworking oil agent and usage thereof

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0797590A (en) * 1993-09-28 1995-04-11 Nisshin Fine Chem Kk Water-soluble machining and grinding oil
WO2011052637A1 (en) * 2009-10-27 2011-05-05 国立大学法人 鹿児島大学 Nanoparticle surface modifying agent, metal nanoparticle, and method of manufacturing nanoparticle surface modifying agent
US9029306B2 (en) 2009-11-30 2015-05-12 Idemitsu Kosan., Ltd. Water-soluble metalworking oil agent and usage thereof

Also Published As

Publication number Publication date
JP3006878B2 (en) 2000-02-07

Similar Documents

Publication Publication Date Title
CN110452766B (en) Fully-synthetic environment-friendly cutting fluid for aluminum alloy processing and preparation method thereof
US4146488A (en) Metal lubricants
JP5658262B2 (en) Cutting fluid with improved performance
CN114805770A (en) Polyether ester lubricant and preparation method thereof
JPH025799B2 (en)
CN111154529A (en) Hard water resistant vegetable oil emulsifying complexing agent and preparation thereof
JPH04202298A (en) Water soluble cutting oil
CN105001952B (en) A kind of aerolite high-speed milling Water-soluble cutting oil and preparation method thereof
EP1444313A2 (en) Method for working or forming metals in the presence of aqueous lubricants based on methanesulphonic acid
KR20200096783A (en) Maleated Soybean Oil Derivatives as Additives in Metalworking Oils
JPH0525483A (en) Water-soluble metal working oil
CH633311A5 (en) SALTS OF HALOGENATED POLYCONDENSATES OF ALCOHOL-FATTY ACIDS USEFUL FOR THE PRODUCTION OF AQUEOUS FLUIDS FOR METAL MACHINING.
CN111205442A (en) Preparation method of clean type metal working fluid modified ricinoleate additive
WO2000052230A1 (en) Corrosion inhibitor and process
CN117844559A (en) Novel antirust emulsified oil and preparation method thereof
CN112680271B (en) Water-based lubricant for high-speed pop can
JPS62149794A (en) Lubricating oil
CN110819430B (en) Environment-friendly total-synthesis metal cutting fluid and preparation method thereof
JPS6121595B2 (en)
JP3964965B2 (en) Method for stabilizing oil-in-water emulsion antifoam composition
JP2000313975A (en) Discoloration preventive agent for aluminum alloy and aluminum
JPH02277536A (en) Water soluble surfactant composition
JPS62177097A (en) Lubrication oil
SU1122488A1 (en) Fluid for vibratory abrasive machining of steel parts
JPH02119925A (en) Water soluble surfactant composition

Legal Events

Date Code Title Description
R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20071126

Year of fee payment: 8

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20081126

Year of fee payment: 9

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20081126

Year of fee payment: 9

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20091126

Year of fee payment: 10

LAPS Cancellation because of no payment of annual fees