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JPH051316B2 - - Google Patents
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JPH051316B2 - - Google Patents

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Publication number
JPH051316B2
JPH051316B2 JP59184375A JP18437584A JPH051316B2 JP H051316 B2 JPH051316 B2 JP H051316B2 JP 59184375 A JP59184375 A JP 59184375A JP 18437584 A JP18437584 A JP 18437584A JP H051316 B2 JPH051316 B2 JP H051316B2
Authority
JP
Japan
Prior art keywords
cutting
water
grinding
performance
oil
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 - Fee Related
Application number
JP59184375A
Other languages
Japanese (ja)
Other versions
JPS6162598A (en
Inventor
Chuichi Watabe
Yoshinobu Hayakawa
Takashi Tokue
Makoto Yoshino
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.)
Toho Chemical Industry Co Ltd
Original Assignee
Toho Chemical Industry 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 Toho Chemical Industry Co Ltd filed Critical Toho Chemical Industry Co Ltd
Priority to JP18437584A priority Critical patent/JPS6162598A/en
Publication of JPS6162598A publication Critical patent/JPS6162598A/en
Publication of JPH051316B2 publication Critical patent/JPH051316B2/ja
Granted legal-status Critical Current

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  • Lubricants (AREA)

Description

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

本発明は鉄鋼、機械、自動車等の製造分野に於
て使用される金属材料の切削及び研削油剤に関す
るものであり、さらにくわしくは、微生物に起因
する腐敗及び品質劣化の防止されたエマルシヨン
型及びソリユーシヨン型の切削及び研削油剤の製
造に関するものである。 鉄鋼、機械、自動車等の製造、加工業及びその
関連工業分野に於て、各種金属材料の切削及び研
削作業に使用される油剤は、従来、不水溶性油剤
が多用されてきたが、近年、職場作業環境の改
善、火災防止、省資源及び経費節約等の生産合理
化をすすめるため、水に可溶性のエマルシヨン型
及びソリユーシヨン型の切削・研削油剤の導入が
行なわれ、最近に至りようやく、その使用量が増
大する傾向にある。 水溶性切削・研削油剤は一般的に、不水溶性油
剤に比較して潤滑剤、極圧添加剤、防錆剤、およ
び防食剤等の各成分等が微粒子状となつて水中に
分散又は可溶化して、切削・研削性能を発揮する
ので、安定な乳化又は可溶化状態が要求され、か
つ良好な切削・研削性能、工具寿命の保持、防錆
性能、金属変色防止能、消泡能、低い皮膚刺激性
及び廃液処理性能等、特別な諸性質を具備するこ
とが求められてきた。従来から、このような水溶
性油剤として、パラフイン系又はナフテン系鉱物
油よりなるベースオイルを主体とし、これに硫
黄、塩素及び燐を含有する極圧添加剤の他、防食
剤として銅合金の切削・研削にはベンゾトリアゾ
ール及びその誘導体、油性向上剤として、脂肪酸
エステル類、植物系及び動物系油脂類、防腐剤と
してはチアゾール系又はトリアジン系殺菌剤、及
び乳化剤として脂肪酸塩、石油スルホネート、脂
肪酸アルカノールアミド、ポリオキシエチレン系
ノニオン性界面活性剤等が選択されて配合されて
きた。 しかしながら、この水溶性油剤は、実際の使用
に当つては、1〜10%程度のエマルシヨン又はソ
リユーシヨンとして1ケ年以上の長期にわたつて
使用されるので、その間、前工程に使用された油
剤の混入、工作機械からの作動油、潤滑油、なら
びに防錆油等の流入及び空中や環境から生ずる微
生物汚染のために、細菌、酵母及び糸状菌の微生
物に起因する腐敗と油剤性能の劣化、発錆及び悪
臭発生の他、エマルシヨンの分離、粘着物質の発
生、PHの低下等が生じ、解決すべき問題として残
されてきた。このような切削・研削油剤のエマル
シヨン又はソリユーシヨンの微生物汚染防止のた
めに、従来、例えばトリスヒドロキシエチル−ト
リアジン、トリスヒドロキシメチルニトロメタ
ン、1,2−ベンズイソチアゾリン−3−オン、
2−メチル−4−イソチアゾリン−3−オン等の
殺菌剤や防腐剤、アルカノールアミン及び荷性カ
リ又は荷性ソーダ等のPH向上剤が使用されてきた
が、これら添加剤の効果は短時間にすぎず、多量
に使用する場合には、薬品臭の発生、毒性の増
大、切削・研削性能の低下、廃液処理性の低下な
ど新たなトラブルの原因となる場合が多かつた。 本発明者等は、水溶性切削・研削油剤の金属加
工現場に於る微生物汚染の問題を解決すべく、研
究を続けた結果、微生物汚染の主要な原因が、水
溶性切削・研削油剤中にベースオイルとして多量
に含まれるパラフイン系及びナフテン系鉱物油の
汚染微生物の資化に基づく著しい増殖にあること
を見い出すと共に、微生物に資化され難いベース
オイルとして分岐型構造を有する合成油、即ち、
ポリプロピレン、ポリブテン及びこれら重合体と
ベンゼンから合成される分岐型アルキルベンゼン
を用いることによつて、従来、殺菌剤や防腐剤及
びPH向上剤の使用では解決することが困難であつ
た、長期に渡る微生物汚染を防止する方法を見い
出して本発明を完成するに至つたものである。即
ち、本発明は水溶性切削・研削油剤のベースオイ
ルとして、ポリプロピレン、ポリブテン及びこれ
ら重合体から誘導される分岐型アルキルベンゼン
が汚染微生物による資化をうけず、かつ、金属材
料の切削・研削性能を有しているという知見に基
づくものである。 本発明にかかるポリプロピレンはプロピレンモ
ノマーの重合により、又ポリブテンはイソブチレ
ンとノルマルブテンの共重合により容易に合成さ
れる。又分岐型アルキルベンゼンはポリプロピレ
ン及びポリブテンとベンゼンからフリーデル・ク
ラフツ反応により合成されることはすでに衆知の
事実である。これら重合体はその重合度を変える
ことにより任意の粘度のものを得ることが出来る
が、本発明にかかる切削・研削油剤のベースオイ
ルとしては一般に5〜150cst(40℃)のものが適
用されるが、実用上、好ましくは特に20〜100cst
(40℃)の重合体が適合する。 しかし、この粘度範囲に本発明の趣旨を限定す
べきではない。 次に、本発明にかかる切削・研削油剤の一般的
配合比率は次の通りであるが、これに限定される
ものではない。 ポリプロピレン、ポリブテン又 は分岐型アルキルベンゼン(粘 度20〜100cst、於40℃) 40〜75% 脂肪酸及び脂肪酸アミド 5〜15% 石油スルホネート 5〜10% ポリオキシエチレンのエーテル 又はエステル型非イオン界面活性剤 5〜10% {アルカノールアミン及び無機アルカリ}
5〜10% 防腐剤 0〜3% 防食剤、消泡剤等の添加剤 0〜5% 水 0〜5% この他、極圧添加剤や各種インヒビターを配合
することも出来る。 次に、本発明にかかる代表的実施例及び従来、
使用されてきた鉱物油を含有する比較例を示して
説明する。
The present invention relates to cutting and grinding fluids for metal materials used in the manufacturing fields of steel, machinery, automobiles, etc., and more specifically to emulsion molds and solutions that prevent spoilage and quality deterioration caused by microorganisms. This invention relates to mold cutting and production of grinding fluid. Traditionally, water-insoluble oils have been widely used for cutting and grinding various metal materials in the manufacturing, processing, and related industries of steel, machinery, automobiles, etc., but in recent years, Water-soluble emulsion-type and solution-type cutting and grinding fluids have been introduced in order to promote production rationalization such as improving the workplace environment, preventing fires, and saving resources and costs. is on the rise. Compared to water-insoluble oils, water-soluble cutting/grinding fluids generally contain ingredients such as lubricants, extreme pressure additives, rust preventives, and anticorrosive agents in the form of fine particles that can be dispersed or dissolved in water. Since it dissolves and exhibits cutting and grinding performance, a stable emulsified or solubilized state is required, as well as good cutting and grinding performance, tool life retention, rust prevention performance, ability to prevent metal discoloration, defoaming ability, There has been a demand for special properties such as low skin irritation and waste liquid treatment performance. Conventionally, such water-soluble oils have mainly been based on paraffinic or naphthenic mineral oils, and in addition to extreme pressure additives containing sulfur, chlorine, and phosphorus, they have also been used as anticorrosive agents for cutting copper alloys. Benzotriazole and its derivatives are used for grinding, fatty acid esters, vegetable and animal fats and oils are used as oil improvers, thiazole or triazine fungicides are used as preservatives, and fatty acid salts, petroleum sulfonates, fatty acid alkanolamides are used as emulsifiers. , polyoxyethylene-based nonionic surfactants, etc. have been selected and blended. However, in actual use, this water-soluble oil agent is used as a 1-10% emulsion or solution for a long period of one year or more, so during that time, the oil agent used in the previous process is lost. Contamination, inflow of hydraulic oil, lubricating oil, anti-corrosion oil, etc. from machine tools, and microbial contamination from the air and environment can cause spoilage and deterioration of oil performance due to microorganisms such as bacteria, yeast, and filamentous fungi. In addition to the generation of rust and bad odors, separation of emulsions, generation of sticky substances, and decrease in pH have occurred, and these problems remain to be solved. In order to prevent microbial contamination of such emulsions or solutions of cutting and grinding fluids, conventionally, for example, trishydroxyethyl-triazine, trishydroxymethylnitromethane, 1,2-benzisothiazolin-3-one,
Bactericides and preservatives such as 2-methyl-4-isothiazolin-3-one, alkanolamines, and PH improvers such as potassium or soda have been used, but the effects of these additives are short-lived. However, when used in large quantities, it often causes new problems such as the generation of chemical odor, increased toxicity, decreased cutting and grinding performance, and decreased waste liquid treatment performance. In order to solve the problem of microbial contamination of water-soluble cutting and grinding fluids at metal processing sites, the present inventors continued their research and found that the main cause of microbial contamination was found in water-soluble cutting and grinding fluids. It has been found that paraffinic and naphthenic mineral oils, which are contained in large amounts as base oils, have significantly proliferated due to the assimilation of contaminant microorganisms, and synthetic oils with a branched structure as base oils that are difficult to be assimilated by microorganisms, i.e.
By using polypropylene, polybutene, and branched alkylbenzenes synthesized from these polymers and benzene, we can eliminate the long-term effects of microorganisms, which were previously difficult to solve with the use of disinfectants, preservatives, and PH improvers. The present invention was completed by discovering a method for preventing contamination. That is, the present invention uses polypropylene, polybutene, and branched alkylbenzenes derived from these polymers as base oils for water-soluble cutting/grinding fluids that are not assimilated by contaminating microorganisms and have the ability to cut and grind metal materials. This is based on the knowledge that Polypropylene according to the present invention can be easily synthesized by polymerizing propylene monomers, and polybutene can be easily synthesized by copolymerizing isobutylene and normal butene. It is already a well-known fact that branched alkylbenzene can be synthesized from polypropylene, polybutene, and benzene by a Friedel-Crafts reaction. These polymers can have any viscosity by changing their degree of polymerization, but base oils of 5 to 150 cst (40°C) are generally used as the base oil for cutting and grinding fluids according to the present invention. , practically preferably especially 20~100cst
(40℃) polymers are suitable. However, the spirit of the present invention should not be limited to this viscosity range. Next, the general compounding ratio of the cutting/grinding fluid according to the present invention is as follows, but is not limited thereto. Polypropylene, polybutene or branched alkylbenzene (viscosity 20-100 cst, at 40°C) 40-75% Fatty acid and fatty acid amide 5-15% Petroleum sulfonate 5-10% Polyoxyethylene ether or ester type nonionic surfactant 5- 10% {alkanolamine and inorganic alkali}
5 to 10% Preservative 0 to 3% Additives such as anticorrosion agents and antifoaming agents 0 to 5% Water 0 to 5% In addition, extreme pressure additives and various inhibitors can also be blended. Next, typical embodiments according to the present invention and conventional methods,
A comparative example containing mineral oil that has been used will be shown and explained.

【表】【table】

【表】【table】

【表】 1 試験方法 (1) 防腐性試験法 空気導入管を装着した1の坂口フラスコに上
記実施例及び比較例の3%エマルシヨン(水道水
使用)500ml、鋳鉄(FC−20)粉10gr、アルミ合
金粉10gr、及び加工現場より採取した、腐敗した
切削油剤エマルシヨン(生菌数8×108個/ml,
PH7.1)20mlを入れて混合した後、37℃で振盪培
養器(行路8cm)を用いて毎分0.5の空気を吹
込みつつ、12時間振盪培養し、次いで空気の吹込
みを停止し12時間静置させた。毎日この操作を繰
り返し、3日毎に上記腐敗液5mlを添加した。こ
の試験培養液は1週間毎にPH(ガラス電極PHメー
ター)及び生菌数(平板寒天培地法)を測定し
た。 (2) 切削性能試験 3トン立型内面引抜きブローチ盤、工具
(SKH55のキーブローチ工具幅7mm、ピツチ幅8
mm)及び被削剤(S45C、硬度HRC1619、円筒外
径50mm、内径25.3mm、高さ20mm)を用いた。切削
条件は速度2m/min、切削刃42枚、1枚当り最
大切込0.05mm、仕上げ4枚で行つた。 加工部分へは実施例及び比較例の3%エマルシ
ヨン(水道水使用)を流し切削した。切削性能は
切削抵抗(ロードセル方式)と仕上面粗さ(触針
式表面粗さ測定器)を測定して示した。 2 試験結果
[Table] 1 Test method (1) Preservative test method 500 ml of the 3% emulsion (using tap water) of the above examples and comparative examples, 10 gr of cast iron (FC-20) powder, 10g of aluminum alloy powder and rotten cutting oil emulsion collected from the processing site (number of viable bacteria: 8 x 10 8 cells/ml,
After adding 20 ml of PH7.1) and mixing, culture with shaking at 37°C for 12 hours while blowing air at a rate of 0.5 per minute using a shaking incubator (path 8 cm), then stop blowing air. Let stand for a while. This operation was repeated every day, and 5 ml of the above-mentioned putrefaction liquid was added every three days. The pH (glass electrode PH meter) and viable cell count (plate agar medium method) of this test culture solution were measured every week. (2) Cutting performance test 3-ton vertical internal drawing broaching machine, tools (SKH55 key broach tool width 7 mm, pitch width 8
mm) and cutting material (S45C, hardness HRC1619, cylinder outer diameter 50 mm, inner diameter 25.3 mm, height 20 mm) were used. The cutting conditions were a speed of 2 m/min, 42 cutting blades, a maximum cutting depth of 0.05 mm per blade, and 4 finishing blades. The 3% emulsions (tap water used) of Examples and Comparative Examples were poured into the processed parts and cut. Cutting performance was shown by measuring cutting resistance (load cell method) and finished surface roughness (stylus surface roughness measuring device). 2 Test results

【表】【table】

【表】【table】

【表】 上記結果が示すように、本発明にかかる水溶性
切削・研削油剤は、従来の鉱物油を含有する油剤
よりも切削性能及び防腐性能に於て優れた効果を
有することが明らかである。
[Table] As shown by the above results, it is clear that the water-soluble cutting/grinding fluid according to the present invention has superior effects on cutting performance and antiseptic performance compared to conventional fluids containing mineral oil. .

Claims (1)

【特許請求の範囲】[Claims] 1 ポリプロピレン、ポリブテン又は、これらの
重合体とベンゼンから合成される分岐型アルキル
ベンゼンをベースオイルとして含有することを特
徴とする、防腐性の良好なる水溶性切削・研削油
剤。
1. A water-soluble cutting/grinding fluid with good antiseptic properties, characterized by containing polypropylene, polybutene, or a branched alkylbenzene synthesized from a polymer thereof and benzene as a base oil.
JP18437584A 1984-09-05 1984-09-05 Water-soluble cutting and grinding oil having improved rotting resistance Granted JPS6162598A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP18437584A JPS6162598A (en) 1984-09-05 1984-09-05 Water-soluble cutting and grinding oil having improved rotting resistance

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP18437584A JPS6162598A (en) 1984-09-05 1984-09-05 Water-soluble cutting and grinding oil having improved rotting resistance

Publications (2)

Publication Number Publication Date
JPS6162598A JPS6162598A (en) 1986-03-31
JPH051316B2 true JPH051316B2 (en) 1993-01-07

Family

ID=16152107

Family Applications (1)

Application Number Title Priority Date Filing Date
JP18437584A Granted JPS6162598A (en) 1984-09-05 1984-09-05 Water-soluble cutting and grinding oil having improved rotting resistance

Country Status (1)

Country Link
JP (1) JPS6162598A (en)

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1413137A (en) * 1921-05-16 1922-04-18 Sheinman Morris Lock
JPS52114602A (en) * 1976-03-23 1977-09-26 Idemitsu Kosan Co Ltd Lubricant composition

Also Published As

Publication number Publication date
JPS6162598A (en) 1986-03-31

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