Deprecated: The each() function is deprecated. This message will be suppressed on further calls in /home/zhenxiangba/zhenxiangba.com/public_html/phproxy-improved-master/index.php on line 456
JPH0571638B2 - - Google Patents
[go: Go Back, main page]

JPH0571638B2 - - Google Patents

Info

Publication number
JPH0571638B2
JPH0571638B2 JP63265026A JP26502688A JPH0571638B2 JP H0571638 B2 JPH0571638 B2 JP H0571638B2 JP 63265026 A JP63265026 A JP 63265026A JP 26502688 A JP26502688 A JP 26502688A JP H0571638 B2 JPH0571638 B2 JP H0571638B2
Authority
JP
Japan
Prior art keywords
weight
carbon atoms
parts
acid
unsaturated aliphatic
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
JP63265026A
Other languages
Japanese (ja)
Other versions
JPH02113082A (en
Inventor
Hideo Shibata
Masahiro Ama
Kojiro Fujita
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.)
DAIDO KAGAKU KOGYO
Original Assignee
DAIDO KAGAKU KOGYO
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 DAIDO KAGAKU KOGYO filed Critical DAIDO KAGAKU KOGYO
Priority to JP63265026A priority Critical patent/JPH02113082A/en
Publication of JPH02113082A publication Critical patent/JPH02113082A/en
Priority to JP5088149A priority patent/JPH0739588B2/en
Publication of JPH0571638B2 publication Critical patent/JPH0571638B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Lubricants (AREA)

Description

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

〔産業上の利用分野〕 本発明は水溶性切削、研削用組成物に関し、さ
らに詳しくはステンレス等のベルト研削に使用す
る水溶性切削、研削用組成物に関する。 〔従来技術〕 一般にステレンス鋼板や鋼帯を製造するに際し
ては、その製造工程中、熱間圧延後のコイル粗研
磨工程、および調質圧延に引き続くコイル仕上研
磨工程が行われ、これ等工程に於いては、従来鉱
物油を主体とするベルト研削油が使用されて来
た。この従来のベルト研削油は研削中に火花が多
発し、火災の危険があり、またミストが発生し作
業環境を著しく悪くする難点があり、特に前者の
コイル粗研摩工程ではコイル板表面が粗くまたは
研削取代が大きいためにこの難点が極めて重大な
問題となつていた。 これに対し、水溶性研削油は火災およびミスト
の問題はないが、研削性が低く、研削ベルトの早
期交換が必要となり、製造コストの増大を来た
し、このため従来は、水溶性研削油は殆んど用い
られず、専らら鉱物油を主体とする研削油いわゆ
るニート油が使用されてきた。 〔発明が解決しようとする課題〕 本発明が解決しようとする課題は、上記従来の
ニート油の欠点を解決することである。 〔課題を解決するための手段〕 本発明者は上記課題を解決するために鋭意検討
した結果、遂に下記に示す特定の成分の特定量含
有する組成物が上記課題を解決出来ること、即ち
水溶性でありながら研削性能が優れ、研削ベルト
の早期交換を必要としない優れた水溶性切削、研
削用組成物となり得ることを見出した。尚水溶性
であるため火災の危険がなく、しかもミストの発
生のないことは勿論である。 即ち本発明は(A)(イ) 炭素数12〜18の脂肪族アル
コール (ロ) 炭素数12〜18の脂肪族アミド、及び (ハ) グリセリンのエチレンオキサイドプロピレ
ンオキサイド付加物であつて、その分子量が
1000〜10000の範囲にあるもの から選ばれた少なくとも1種3〜50重量部 (B)(ニ) 炭素数11〜22の不飽和カルボン酸、又は (ホ) 上記(ニ)のカルボン酸に、炭素数11〜22の飽
和又は不飽和脂肪族カルボン酸と炭素数1〜
22の飽和又は不飽和脂肪族アルコールとのエ
ステル(但し、カルボン酸又はアルコールの
少なくとも一方が不飽和脂肪族基を有する)
の少なくとも1種を酸価が20mgKOH/g以
上となる様に混合した混合物、 にその3〜25重量%の硫黄を付加した有機硫黄
化合物の少なくとも1種1〜30重量部、及び (C) アルカノールアミン1〜30重量部 を主成分として成ることを特徴とする水溶性切
削、切削用組成物に係るものである。 〔発明の作用並びに構成〕 本発明の組成物は基本的には、上記(A)、(B)及び
(C)成分を含有して成るものであり、これ等(A)〜(C)
の各成分を上記特定量含有せしめることにより、
はじめて優れた切削、研削特性を発揮し、惹いて
は研削エルトの早期交換が不要となる。また水溶
性であるために火災の危険がなく、ミストも発生
しない。この際上記(A)〜(C)の各成分のうちどれ1
つが欠けても上記優れた効果は発揮されず、更に
は上記3成分を上記特定割合で併用しなければ上
記優れた効果が損なわれる傾向が生じる。 先ず本発明の(A)成分から説明する。 本発明に於いて使用する脂肪族アルコールは炭
素数12〜18のものを使用し飽和ばかりでなく不飽
和脂肪族アルコールをも包含する。また1価アル
コールばかりでなく、多価アルコールも使用する
ことが出来、更にはOH基等適宜な置換等が置換
したものも使用出来、たとえばオキソアルコール
等も使用することが出来る。好ましい具体例は、
例えばラウリルアルコール、オレイルアルコー
ル、ステアリルアルコール、オキソアルコール、
トリメチロールプロパン等である。 脂肪族アミドは炭素数12〜18のものであつて、
その脂肪族基としては飽和ばかりでなく不飽和の
ものでも良い。またアミドとしては1級アミドば
かりでなく、2〜3級アミドも包含され、更には
OH基等が置換していても良い。好ましい具体例
として例えばラウリルアミド、オレイルアミド、
ステリルアミド、オキソアルコールアミド等を使
用することができる。 この炭素数12〜18の脂肪族アルオール又は(及
び)脂肪族アミドは主に研削性を賦与するための
成分であり、いずれに於いても炭素数が12に達し
ないと研削性が不足し、また炭素数が18より大き
くなると流動性が低下する傾向がある。 次にグリセリンのエチレンオキシドプロピレン
オキシド(以下EOPOと略記する)付加物につい
て説明するが、この付加物もやはり主に研削性を
賦与するために使用される成分であり、その分子
量は1000〜10000の範囲のものを使用する。分子
量が1000に達しないと研削性が不足し、10000よ
り多くなると溶解性が低下する。またエチレンオ
キシドとプロピレンオキシドの割合はエチレンオ
キシドが30〜90重量%好ましくは40〜60重量%で
あつてエチレンオキシドが30重量%未満では溶解
性が不足し、90重量%以上では研削性が不足す
る。 本発明に於いてはこの(A)成分としては上記(イ)〜
(ハ)の各成分の1種また2種以上が併用され、その
使用量は3〜50重量部好ましくは5〜40重量部で
ある。3重量部に達しないと研削性が不足し、50
重量部より多くなると溶解性が低下する。 次いで(B)成分について説明する。 この(B)成分は主に極圧性を付与することにより
研削性能を向上せしめる目的で使用され、その使
用量は1〜30重量部である。この際1重量部未満
では研削性が不足し、30重量部より多いと溶解性
が低下する。 この(B)成分を大別すると1つは炭素数11〜22の
不飽和カルボン酸に3〜25%の硫黄を付与せしめ
た反応生成物であり、他の1つは上記のカルボン
酸に、炭素数11〜22の飽和又は不飽和脂肪族カル
ボン酸と炭素数1〜22の飽和又は不飽和脂肪族ア
ルコールとのエステル(但しカルボン酸又はアル
コールの少なくとも一方が不飽和脂肪族基を有す
る)の少なくとも1種を酸価が20mgKOH/g以
上となる様に混合した混合物に、その3〜25重量
%の硫黄を付与した反応生成物である。尚3〜25
重量%とは硫黄付与物中の硫黄の量が3〜25重量
%であることを示す。ここで使用する炭素数11〜
22の不飽和脂肪族カルボン酸としては一塩基酸ば
かりでなく多塩基酸も使用され、また置換基たと
えばOH基その他の基が置換していても良い。好
ましい具体例としてたとえばウンデシレン酸、オ
レイン酸、エルシン酸酸、リノール酸、リノレン
酸、エレオステアリン酸、リシノレイン酸、エラ
イジン酸、リンデル酸、アラキドン酸等が例示で
きる。 また上記エステルを構成する一成分である炭素
数11〜22の不飽和脂肪酸カルボン酸としては、不
飽和脂肪族カルボン酸は上記と同様のものが使用
され、また飽和脂肪族カルボン酸としては一塩基
酸ばかりでなく、多塩基酸も使用出来、またまた
必要に応じOH基等適宜な置換基が置換していて
も良い。代表的な具体例としては、ラウリン酸、
トリデシル酸、ミリスチン酸、ペンタデシル酸、
パルミチン酸、ステアリン酸、ノナデシル酸、ベ
ヘン酸、エイコサノイツク酸等が例示できる。 上記エステルの他の一成分たる飽和または不飽
和アルコールとしてはその炭素数が1〜22の1価
または多価アルコールが使用される。好ましい具
体例としてはたとえばメチルアクローク、エチル
アルコール、ブチルアルコール、ヘキシルアルコ
ール、オクチルアノール、ラウリルアルコール、
オレイルアルコール、ステアリルアルコール、オ
キソアルコール等が例示できる。 上記エステルとては特い上記カルボン酸または
アルコールの少なくともいずれか一方が不飽和脂
肪族基であることが必須である。この際いずれも
が飽和脂肪族基の場合には硫黄が反応しないた
め、目的の添加剤にならないので好ましくない。 このエステルは上記炭素数11〜22の不飽和脂肪
族族カルボン酸に、得られる混合物の酸価が20mg
KOH/g以上となるように混合される。この際
の酸価が上記値に達しないと水溶性が低下する。 本発明に於ける(B)成分は上記不飽和脂肪族カル
ボン酸、または上記混合物に3〜25重量%の硫黄
を付加せしめた反応物であり、この反応は以下の
様にして行われる。即ちこの硫黄付加反応は無溶
媒、反応温度90〜120℃、反応時間30分〜2時間
の条件下、該カルボン酸または混合物に対し、硫
黄付加量が3〜25好ましくは5〜20重量%になる
様に反応させる。ここで硫黄付加量が3重量%に
達しないと研削性が不足し、25重量%よい多くな
ると臭気が大となるので好ましくない。 上記反応を、オレイン酸(CH3(CH26−CH2
=CH−CH2−(CH26−COOH)を代表例として
とりあげて説明すれば以下の通りである。 CH3(CH26をR、CH2(CH26−COOHをR′と
略記すると、オレイン酸はR−CH2−CH=CH
−R′となる。このオレイン酸は硫黄と次の様に
反応すると考えられる。
[Industrial Application Field] The present invention relates to a water-soluble cutting and grinding composition, and more particularly to a water-soluble cutting and grinding composition used for belt grinding of stainless steel and the like. [Prior Art] Generally, when manufacturing stainless steel sheets and steel strips, a coil rough polishing process after hot rolling and a coil finish polishing process following skin pass rolling are performed during the manufacturing process. Conventionally, belt grinding oil mainly composed of mineral oil has been used. This conventional belt grinding oil generates many sparks during grinding, which poses a risk of fire, and also generates mist, which significantly worsens the working environment.Especially in the former coil rough polishing process, the coil plate surface is rough or Since the grinding allowance is large, this difficulty has become an extremely serious problem. On the other hand, water-soluble grinding oils do not cause the problems of fire and mist, but they have poor grinding properties and require early replacement of the grinding belt, which increases manufacturing costs.For this reason, conventionally, water-soluble grinding oils Grinding oil mainly composed of mineral oil, so-called neat oil, has been used exclusively. [Problem to be Solved by the Invention] The problem to be solved by the present invention is to solve the above-mentioned drawbacks of conventional neat oil. [Means for Solving the Problems] As a result of intensive studies to solve the above problems, the present inventors have finally found that a composition containing a specific amount of the specific components shown below can solve the above problems, that is, water-soluble However, it has been found that it can be an excellent water-soluble cutting and grinding composition that has excellent grinding performance and does not require early replacement of the grinding belt. Since it is water-soluble, there is no danger of fire, and it goes without saying that it does not generate mist. That is, the present invention is an ethylene oxide propylene oxide adduct of (A) (a) an aliphatic alcohol having 12 to 18 carbon atoms, (b) an aliphatic amide having 12 to 18 carbon atoms, and (c) glycerin, the molecular weight of which is but
3 to 50 parts by weight of at least one selected from the following: Saturated or unsaturated aliphatic carboxylic acids having 11 to 22 carbon atoms and 1 to 22 carbon atoms
Esters of 22 with saturated or unsaturated aliphatic alcohols (provided that at least one of the carboxylic acid or alcohol has an unsaturated aliphatic group)
1 to 30 parts by weight of at least one organic sulfur compound to which 3 to 25% by weight of sulfur has been added, and (C) an alkanol. This invention relates to a water-soluble cutting composition characterized by containing 1 to 30 parts by weight of an amine as a main component. [Function and structure of the invention] The composition of the present invention basically comprises the above (A), (B) and
(C) It is composed of components (A) to (C).
By containing each component in the above specified amount,
For the first time, it exhibits excellent cutting and grinding characteristics, which in turn eliminates the need for early replacement of the grinding elt. Furthermore, since it is water-soluble, there is no danger of fire and no mist is generated. In this case, which one of the above ingredients (A) to (C)
Even if the above-mentioned excellent effects are lacking, the above-mentioned excellent effects will not be exhibited, and furthermore, unless the above-mentioned three components are used together in the above-mentioned specific proportions, the above-mentioned excellent effects will tend to be impaired. First, component (A) of the present invention will be explained. The aliphatic alcohol used in the present invention has 12 to 18 carbon atoms, and includes not only saturated aliphatic alcohols but also unsaturated aliphatic alcohols. In addition, not only monohydric alcohols but also polyhydric alcohols can be used, and even those substituted with appropriate substitutions such as OH groups can be used, for example, oxo alcohols can also be used. Preferred specific examples are:
For example, lauryl alcohol, oleyl alcohol, stearyl alcohol, oxo alcohol,
Trimethylolpropane, etc. Aliphatic amides have 12 to 18 carbon atoms,
The aliphatic group may be not only saturated but also unsaturated. In addition, amides include not only primary amides but also secondary to tertiary amides, and
It may be substituted with an OH group or the like. Preferred specific examples include laurylamide, oleylamide,
Sterylamide, oxoalcoholamide, etc. can be used. This aliphatic alol or (and) aliphatic amide having 12 to 18 carbon atoms is a component mainly for imparting grindability, and in either case, if the carbon number does not reach 12, the grindability is insufficient. Furthermore, when the number of carbon atoms exceeds 18, fluidity tends to decrease. Next, we will explain the ethylene oxide propylene oxide (hereinafter abbreviated as EOPO) adduct of glycerin. This adduct is also a component mainly used to impart grindability, and its molecular weight ranges from 1000 to 10000. Use the one. If the molecular weight does not reach 1,000, grindability is insufficient, and if it exceeds 10,000, solubility decreases. The ratio of ethylene oxide to propylene oxide is 30 to 90% by weight, preferably 40 to 60% by weight; if ethylene oxide is less than 30% by weight, the solubility will be insufficient, and if it is more than 90% by weight, the grindability will be insufficient. In the present invention, this (A) component includes the above (a) to
One or more of the components (c) are used in combination, and the amount used is 3 to 50 parts by weight, preferably 5 to 40 parts by weight. If the amount does not reach 3 parts by weight, the grindability will be insufficient, and 50
When the amount exceeds parts by weight, solubility decreases. Next, component (B) will be explained. This component (B) is used mainly for the purpose of improving grinding performance by imparting extreme pressure properties, and the amount used is 1 to 30 parts by weight. In this case, if it is less than 1 part by weight, the grindability will be insufficient, and if it is more than 30 parts by weight, the solubility will be reduced. Broadly speaking, component (B) is a reaction product obtained by adding 3 to 25% sulfur to an unsaturated carboxylic acid having 11 to 22 carbon atoms, and the other is a reaction product obtained by adding 3 to 25% sulfur to the above carboxylic acid. Esters of saturated or unsaturated aliphatic carboxylic acids having 11 to 22 carbon atoms and saturated or unsaturated aliphatic alcohols having 1 to 22 carbon atoms (provided that at least one of the carboxylic acid or the alcohol has an unsaturated aliphatic group) It is a reaction product obtained by adding 3 to 25% by weight of sulfur to a mixture of at least one substance having an acid value of 20 mgKOH/g or more. Nao 3-25
% by weight indicates that the amount of sulfur in the sulfur additive is 3 to 25% by weight. The number of carbons used here is 11~
Not only monobasic acids but also polybasic acids are used as the unsaturated aliphatic carboxylic acids of 22, and they may be substituted with substituents such as OH groups and other groups. Preferred specific examples include undecylenic acid, oleic acid, erucic acid, linoleic acid, linolenic acid, eleostearic acid, ricinoleic acid, elaidic acid, Linderic acid, arachidonic acid, and the like. In addition, as the unsaturated fatty acid carboxylic acid having 11 to 22 carbon atoms, which is one of the components constituting the above ester, the same unsaturated aliphatic carboxylic acids as mentioned above are used, and as the saturated aliphatic carboxylic acid, monobasic Not only acids but also polybasic acids can be used, and if necessary, suitable substituents such as OH groups may be substituted. Typical specific examples include lauric acid,
tridecylic acid, myristic acid, pentadecylic acid,
Examples include palmitic acid, stearic acid, nonadecylic acid, behenic acid, and eicosanoic acid. As the saturated or unsaturated alcohol which is another component of the above ester, a monohydric or polyhydric alcohol having 1 to 22 carbon atoms is used. Preferred specific examples include methyl alcohol, ethyl alcohol, butyl alcohol, hexyl alcohol, octyl anol, lauryl alcohol,
Examples include oleyl alcohol, stearyl alcohol, and oxo alcohol. In the above-mentioned ester, it is essential that at least one of the above-mentioned carboxylic acid or alcohol is an unsaturated aliphatic group. In this case, if both groups are saturated aliphatic groups, the sulfur will not react with the group, and the target additive will not be used, which is not preferable. This ester is added to the above unsaturated aliphatic carboxylic acid having 11 to 22 carbon atoms, and the acid value of the resulting mixture is 20 mg.
They are mixed so that the concentration is KOH/g or more. If the acid value at this time does not reach the above value, the water solubility will decrease. Component (B) in the present invention is a reaction product obtained by adding 3 to 25% by weight of sulfur to the above-mentioned unsaturated aliphatic carboxylic acid or the above-mentioned mixture, and this reaction is carried out as follows. That is, this sulfur addition reaction is carried out without a solvent, at a reaction temperature of 90 to 120°C, and a reaction time of 30 minutes to 2 hours, and the amount of sulfur added is 3 to 25% by weight, preferably 5 to 20% by weight, based on the carboxylic acid or mixture. React as you see fit. If the amount of sulfur added does not reach 3% by weight, the grindability will be insufficient, and if it exceeds 25% by weight, the odor will increase, which is not preferable. The above reaction is performed using oleic acid (CH 3 (CH 2 ) 6 −CH 2
=CH- CH2- ( CH2 ) 6 -COOH) as a representative example. When CH 3 (CH 2 ) 6 is abbreviated as R and CH 2 (CH 2 ) 6 -COOH is abbreviated as R', oleic acid is R-CH 2 -CH=CH
−R′. It is thought that this oleic acid reacts with sulfur in the following manner.

【表】 ↓
R−CH−CH=CH−R′

S

R−CH−CH=CH−R′
本発明に於いて使用する(C)成分たるアルカノール
アミンは主に(B)成分と反応してアミン塩とし水に
可溶なものとする目的で使用され、その塩用量は
1〜30重量部である。この際1重量部未満では、
(B)成分の溶解性が低下する傾向が生じ、30重量部
より多くなると添加効果が少なくなる傾向が生ず
る。アルカノールアミンは具体的には、たとえば
モノエタノールアミン、ジエタノールアミン、ト
リエタノールアイン、N,Nジメチルエタノール
アミン、N,Nジエチルエタノールアミン、N,
Nジイソプロピルエタノールアミン、N−(β−
アミノエチル)エタノールアミン、N−メチルメ
タノールアミン、N・N−ビス(β−アミノエチ
ル)エタノールアミン等が例示できる。 本発明水溶性切削、研削組成物は上記(A)(B)及び
(C)成分が必須であるが、この他に必要に応じて塩
素系または硫黄系極性添加剤例えば塩素化脂肪
酸、塩素化油脂、塩素化パラフイン、硫黄化脂肪
酸等が、またその他油脂も配合することが出来
る。またその他この種組成物に従来から使用され
て来た各種の添加剤を配合することが出来る。 本発明組成物はこれを使用するに際しては適宜
水で希釈して使用するが、使用状態に於いてその
組成物濃度が20〜50重量%程度になるように水に
溶解させることが好ましい。 (実施例) 次に本発明を詳しく説明するため、実施例をあ
げて記述する。 実施例 1〜3 第1表に示す所定の成分を所定量(重量部)混
合して組成物を調製した。 比較例 鉱油92.1重量部、ウールグリース5.6重量部及
びジンクジチオフオスフエート2.3重量部を混合
して組成物を得た。 実施例および比較例の各組成物を下記条件にて
ベルト研削試験を行つた。その結果を第1図に示
す。但し第1図中イ〜ハは順番に実施例1〜3の
組成物を表し、また点線で示したニは比較例の組
成物を表す。 ベルト研削試験条件 試験機:南式平面研磨機 材料送り速度:12m/分 ベルト速度:1200m/分 ベルト寸法:100×2100mm ベルト種:クロスベルト#60(永塚工業製AA−
ERS) 研削圧:20Kg/50mm(W) 研削距離:500mm 被研削材:SUS304 10(t)×50(W)×500()mm コンタクトロール:250mm(φ)、70duro
[Table] ↓
R−CH−CH=CH−R′

S 2

R−CH−CH=CH−R′
The alkanolamine, component (C), used in the present invention is mainly used for the purpose of reacting with component (B) to form an amine salt, which is soluble in water, and the amount of the salt is 1 to 30 parts by weight. It is. In this case, if it is less than 1 part by weight,
The solubility of component (B) tends to decrease, and when the amount exceeds 30 parts by weight, the effect of addition tends to decrease. Specifically, alkanolamines include, for example, monoethanolamine, diethanolamine, triethanolamine, N,N dimethylethanolamine, N,N diethylethanolamine, N,
N-diisopropylethanolamine, N-(β-
Examples include aminoethyl)ethanolamine, N-methylmethanolamine, and N.N-bis(β-aminoethyl)ethanolamine. The water-soluble cutting and grinding composition of the present invention includes the above (A), (B) and
Ingredient (C) is essential, but if necessary, chlorine-based or sulfur-based polar additives such as chlorinated fatty acids, chlorinated fats and oils, chlorinated paraffins, sulfurized fatty acids, etc., and other fats and oils may also be added. I can do it. In addition, various other additives conventionally used in this type of composition can be blended. When using the composition of the present invention, it is diluted with water as appropriate, but it is preferable to dissolve it in water so that the concentration of the composition in use is about 20 to 50% by weight. (Examples) Next, in order to explain the present invention in detail, examples will be given and described. Examples 1 to 3 Compositions were prepared by mixing predetermined amounts (parts by weight) of predetermined components shown in Table 1. Comparative Example A composition was obtained by mixing 92.1 parts by weight of mineral oil, 5.6 parts by weight of wool grease, and 2.3 parts by weight of zinc dithiophosphate. A belt grinding test was conducted on each of the compositions of Examples and Comparative Examples under the following conditions. The results are shown in FIG. However, in FIG. 1, I to C represent the compositions of Examples 1 to 3 in order, and D indicated by a dotted line represents the composition of the comparative example. Belt grinding test conditions Test machine: Southern type surface polisher Material feed speed: 12 m/min Belt speed: 1200 m/min Belt dimensions: 100 x 2100 mm Belt type: Cross belt #60 (Nagatsuka Kogyo AA-
ERS) Grinding pressure: 20Kg/50mm(W) Grinding distance: 500mm Material to be ground: SUS304 10(t)×50(W)×500()mm Contact roll: 250mm(φ), 70duro

【表】 但し第1表中の次の記載は以下のことを表
す。 TEA:トリエタノールアミン TIPA:トリイソプロピルアミン
[Table] However, the following description in Table 1 represents the following. TEA: Triethanolamine TIPA: Triisopropylamine

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は各組成物のベルト研削試験の結果を
表す。
FIG. 1 represents the results of belt grinding tests for each composition.

Claims (1)

【特許請求の範囲】 1 (A)(イ) 炭素数12〜18の脂肪族アルコール、 (ロ) 炭素数12〜18の脂肪酸アミド、及び (ハ) グリセリンのエチレンオキサイドプロピレ
ンオキサイド付加物であつて、その分子量が
1000〜10000の範囲にあるもの から選ばれた少なくとも1種3〜50重量部、 (B)(ニ) 炭素数11〜22の不飽和カルボン酸、又は (ホ) 上記(ニ)のカルボン酸に、炭素数11〜22の飽
和又は不飽和脂肪族カルボン酸と炭素数1〜
22の飽和又は不飽和脂肪族アルコールとのエ
ステル(但し、カルボン酸又はアルコールの
少なくとも一方が不飽和脂肪族基を有する)
の少なくとも1種を酸価が20mgKOH/g以
上となる様に混合した混合物に、無溶媒、90
〜120℃で30分〜2時間の条件下硫黄付加量
が3〜25重量%となるように硫黄を付加した
有機硫黄化合物の少なくとも1種1〜30重量
部、及び (C) アルカノールアミン1〜30重量部を主成分と
して成ることを特徴とする水溶性切削、切削用
組成物。 2 請求項1に記載の組成物を、その使用状態に
於いてその濃度が20〜50重量%になるように水に
溶解させたことを特徴とする切削、切削用組成
物。
[Scope of Claims] 1 (A) (a) an aliphatic alcohol having 12 to 18 carbon atoms; (b) a fatty acid amide having 12 to 18 carbon atoms; and (c) an ethylene oxide propylene oxide adduct of glycerin. , its molecular weight is
3 to 50 parts by weight of at least one selected from the range of 1,000 to 10,000; , a saturated or unsaturated aliphatic carboxylic acid having 11 to 22 carbon atoms and a saturated or unsaturated aliphatic carboxylic acid having 1 to 22 carbon atoms
Esters of 22 with saturated or unsaturated aliphatic alcohols (provided that at least one of the carboxylic acid or alcohol has an unsaturated aliphatic group)
A mixture of at least one of the following with an acid value of 20 mgKOH/g or more, without solvent, 90
1 to 30 parts by weight of at least one organic sulfur compound to which sulfur has been added such that the amount of sulfur added is 3 to 25% by weight under conditions of 30 minutes to 2 hours at ~120°C, and (C) 1 to 30 parts by weight of an alkanolamine. A composition for water-soluble cutting and cutting, characterized by comprising 30 parts by weight as a main component. 2. A composition for cutting or cutting, characterized in that the composition according to claim 1 is dissolved in water so that the concentration thereof in use is 20 to 50% by weight.
JP63265026A 1988-10-20 1988-10-20 Water-soluble cutting and grinding composition Granted JPH02113082A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
JP63265026A JPH02113082A (en) 1988-10-20 1988-10-20 Water-soluble cutting and grinding composition
JP5088149A JPH0739588B2 (en) 1988-10-20 1993-03-22 Water-soluble cutting and grinding composition

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP63265026A JPH02113082A (en) 1988-10-20 1988-10-20 Water-soluble cutting and grinding composition
JP5088149A JPH0739588B2 (en) 1988-10-20 1993-03-22 Water-soluble cutting and grinding composition

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP5088149A Division JPH0739588B2 (en) 1988-10-20 1993-03-22 Water-soluble cutting and grinding composition

Publications (2)

Publication Number Publication Date
JPH02113082A JPH02113082A (en) 1990-04-25
JPH0571638B2 true JPH0571638B2 (en) 1993-10-07

Family

ID=26429584

Family Applications (2)

Application Number Title Priority Date Filing Date
JP63265026A Granted JPH02113082A (en) 1988-10-20 1988-10-20 Water-soluble cutting and grinding composition
JP5088149A Expired - Lifetime JPH0739588B2 (en) 1988-10-20 1993-03-22 Water-soluble cutting and grinding composition

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP5088149A Expired - Lifetime JPH0739588B2 (en) 1988-10-20 1993-03-22 Water-soluble cutting and grinding composition

Country Status (1)

Country Link
JP (2) JPH02113082A (en)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PY970104A (en) * 1996-08-30 2001-12-03 Monsanto Co NEW WATER-SOLUBLE FLUIDS FOR METALWORKING
US6206764B1 (en) * 1997-04-17 2001-03-27 The United States Of America As Represented By The Secretary Of Commerce Methods for machining hard materials using alcohols
JP2000290676A (en) * 1999-04-05 2000-10-17 Idemitsu Kosan Co Ltd Metalworking oil composition
AU765787B2 (en) * 1999-07-21 2003-10-02 Dainippon Ink And Chemicals Inc. Extreme-pressure additive, process for producing the same, cutting fluid, and grinding fluid
JP4761096B2 (en) * 2001-03-30 2011-08-31 Dic株式会社 Method for producing sulfurized hydroxy fatty acid dimer and salt thereof
JP2002294267A (en) * 2001-03-30 2002-10-09 Dainippon Ink & Chem Inc Cutting fluid and grinding fluid
DE102007041372A1 (en) * 2007-08-30 2009-03-05 Technische Universität Braunschweig Carolo-Wilhelmina coolant
JP6979009B2 (en) * 2016-02-16 2021-12-08 出光興産株式会社 Water-soluble metalworking oil composition, metalworking liquid and metalworking method

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5412042B2 (en) * 1973-08-10 1979-05-19
JPS543105A (en) * 1977-06-07 1979-01-11 Dow Chemical Co Oillinnwater type of lubricating and cooling liquid emulsion
JPS5698294A (en) * 1980-01-09 1981-08-07 Honda Motor Co Ltd Water-soluble cutting oil
JPS6024158B2 (en) * 1981-12-23 1985-06-11 キヤタピラ−三菱株式会社 Water-soluble lubricant for tapping process

Also Published As

Publication number Publication date
JPH02113082A (en) 1990-04-25
JPH0673392A (en) 1994-03-15
JPH0739588B2 (en) 1995-05-01

Similar Documents

Publication Publication Date Title
EP0252533B1 (en) A method in the mechanical working of aluminium and aluminium alloys in the presence of a cooling lubricant, and a concentrate of the cooling lubricant
DE69636652T2 (en) THE USE OF BIODEGRADABLE LUBRICANT OIL
JP2004531614A (en) Low and high molecular weight emulsifiers, in particular based on polyisobutylene, and mixtures of said emulsifiers
US2959547A (en) Aqueous coolant for metal working machines
JPH0571638B2 (en)
JP2887403B2 (en) Lubricating fluid
DE3225000C2 (en)
EP0586421B1 (en) Method of producing an amide product mixture, an amide product mixture and the use thereof
KR20230023628A (en) Additives or compositions that impart lubricity
EP2828419B1 (en) Aqueous, surface-active, corrosion protection formulation, and as well as an oil-containing, water-miscible emulsion concentrate
EP0143444A2 (en) Lubricating oil composition for metal rolling
EP0584711A1 (en) Alkenyl succinic acid derivatives as metal working agents
JPH08325588A (en) Cold rolling lubricant for steel plate
JPH08259978A (en) Lubricating composition
JPS633919B2 (en)
JPS6056434B2 (en) Rust preventive manufacturing method
EP0501368B1 (en) Use of alkenylsuccinic acid half-amides
US4956106A (en) Low foaming rust inhibiting composition
JPH0657832B2 (en) Metal rolling oil composition
JP5571971B2 (en) Metalworking oil composition
JPS62112695A (en) Cold rolling oil composition
JPH11323375A (en) Metalworking oil composition
JPH04118101A (en) Cold rolling method
JP2617719B2 (en) Oil-soluble surfactant for metal oils
EP0340498B1 (en) Water-dispersible compositions having a detergent or protective action on steel sheets and a process for their preparation