JP2005314558A - Metalworking oil composition - Google Patents

Metalworking oil composition Download PDF

Info

Publication number
JP2005314558A
JP2005314558A JP2004134470A JP2004134470A JP2005314558A JP 2005314558 A JP2005314558 A JP 2005314558A JP 2004134470 A JP2004134470 A JP 2004134470A JP 2004134470 A JP2004134470 A JP 2004134470A JP 2005314558 A JP2005314558 A JP 2005314558A
Authority
JP
Japan
Prior art keywords
oil
oil composition
metalworking
mass
based metal
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
JP2004134470A
Other languages
Japanese (ja)
Other versions
JP4769426B2 (en
Inventor
Akihiro Shishikura
昭弘 宍倉
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Idemitsu Kosan Co Ltd
Original Assignee
Idemitsu Kosan Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Idemitsu Kosan Co Ltd filed Critical Idemitsu Kosan Co Ltd
Priority to JP2004134470A priority Critical patent/JP4769426B2/en
Priority to CN2005800127410A priority patent/CN1946834B/en
Priority to PCT/JP2005/008139 priority patent/WO2005105962A1/en
Priority to TW094114108A priority patent/TW200609345A/en
Publication of JP2005314558A publication Critical patent/JP2005314558A/en
Application granted granted Critical
Publication of JP4769426B2 publication Critical patent/JP4769426B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M141/00Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential
    • C10M141/10Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential at least one of them being an organic phosphorus-containing compound
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M141/00Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential
    • C10M141/08Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential at least one of them being an organic sulfur-, selenium- or tellurium-containing compound
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/02Water
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/121Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/125Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/129Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more carbon atoms
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/34Esters having a hydrocarbon substituent of thirty or more carbon atoms, e.g. substituted succinic acid derivatives
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/02Sulfur-containing compounds obtained by sulfurisation with sulfur or sulfur-containing compounds
    • C10M2219/024Sulfur-containing compounds obtained by sulfurisation with sulfur or sulfur-containing compounds of esters, e.g. fats
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/08Thiols; Sulfides; Polysulfides; Mercaptals
    • C10M2219/082Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/20Metal working
    • C10N2040/243Cold working
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/20Metal working
    • C10N2040/244Metal working of specific metals
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/20Metal working
    • C10N2040/244Metal working of specific metals
    • C10N2040/245Soft metals, e.g. aluminum
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/20Metal working
    • C10N2040/244Metal working of specific metals
    • C10N2040/246Iron or steel

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Lubricants (AREA)

Abstract

<P>PROBLEM TO BE SOLVED: To provide a metalworking oil composition having excellent workability to a hardly workable material such as iron-based metal material, chromium-based metal material, nickel-based metal material or thick aluminum plate, composed of a non-chlorine working oil and, nevertheless, having a workability superior to a chlorine-based working oil. <P>SOLUTION: The metalworking oil composition contains (B) a bentonite clay mineral treated with an organic material and (C) an active sulfur compound in (A) a base oil. <P>COPYRIGHT: (C)2006,JPO&NCIPI

Description

本発明は、金属加工油組成物、詳しくは難加工材の加工にも適用できる非塩素系金属加工油組成物に関する。   The present invention relates to a metalworking oil composition, and more particularly to a non-chlorine metalworking oil composition that can be applied to processing difficult-to-process materials.

これまで、鉄系金属材、クロム系金属材、ニッケル系金属材、又はアルミ厚板材などの難加工材の加工は、塩素化パラフィンや五塩化ステアリン酸等を含有した塩素系油剤で加工されていた。
ところが、近年、環境問題から塩素含有潤滑油の処理が煩雑且つ高コスト化し、非塩素系金属加工油への転換を余儀なくされている。
そこで、その実現に向け研究開発が進められており、例えば、塩素系基材の代替としてポリサルファイド、硫化油脂、カルシウムスルホネート、Zn−DTP等の硫黄系基材、及びリン酸エステル等のリン系基材を中心に構成された金属加工油(特許文献1〜4参照)、脂肪酸やそのアルカリ土類金属塩、あるいはそのエステル類で構成された油剤(特許文献5,6参照)、シュウ酸等の化成処理材を応用したもの(特許文献7参照)などが提案されている。しかしながら、これらはいずれも、ステンレス鋼等の難加工材とされる加工に対しては、潤滑不良による加工性の低下が著しく、具体的には金型の工具摩耗と表面のかじりキズが発生して、その性能は塩素系油剤の性能に及ばないのが現状である。
そのため、さらなる研究が進められている。
Until now, difficult-to-process materials such as iron-based metal materials, chromium-based metal materials, nickel-based metal materials, and aluminum thick plate materials have been processed with chlorinated oils containing chlorinated paraffin and pentachlorostearic acid. It was.
However, in recent years, the treatment of chlorine-containing lubricating oil has become complicated and expensive due to environmental problems, and it has been forced to switch to non-chlorine metalworking oil.
Therefore, research and development has been promoted to realize this, for example, as a substitute for chlorine-based substrates, polysulfides, sulfurized fats and oils, calcium sulfonates, sulfur-based substrates such as Zn-DTP, and phosphorus-based groups such as phosphate esters. Metal processing oil (see Patent Documents 1 to 4) mainly composed of wood, oils composed of fatty acids and their alkaline earth metal salts or esters (see Patent Documents 5 and 6), oxalic acid, etc. The thing (refer patent document 7) etc. which applied the chemical conversion treatment material are proposed. However, in all of these, for work that is difficult to process such as stainless steel, the workability is significantly reduced due to poor lubrication, and specifically, tool wear on the mold and surface galling are generated. The current performance is not as good as that of chlorinated oils.
Therefore, further research is underway.

特再平8−33253号公報Japanese Patent Publication No.8-33253 特開平9−111278号公報Japanese Patent Laid-Open No. 9-111278 特開2001−49279号公報JP 2001-49279 A 特開2002−155293号公報JP 2002-155293 A 特開2002−38181号公報JP 2002-38181 A 特開2003−49185号公報JP 2003-49185 A 特開2002−88387号公報JP 2002-88387 A

本発明は、上述のような状況下でなされたものであり、鉄系金属材、クロム系金属材、ニッケル系金属材、又はアルミ厚板材などの難加工材に対しても優れた加工性を有し、非塩素系加工油であっても、塩素系加工油より優れた加工性を有する金属加工油組成物を提供することを目的とする。   The present invention has been made under the circumstances as described above, and has excellent workability even for difficult-to-work materials such as iron-based metal materials, chromium-based metal materials, nickel-based metal materials, and aluminum thick plate materials. An object of the present invention is to provide a metalworking oil composition having a processability superior to that of a chlorine-based processing oil, even if it is a non-chlorine-based processing oil.

本発明者らは、前記目的を達成するために鋭意研究を重ねた結果、特定の硫黄
化合物、及び特定の粘土鉱物を配合した金属加工油組成物によって、前記課題を
解決し得ることを見出した。本発明は、かかる知見に基づいて完成したものであ
る。
As a result of intensive studies to achieve the above object, the present inventors have found that the above problems can be solved by a metalworking oil composition containing a specific sulfur compound and a specific clay mineral. . The present invention has been completed based on such findings.

すなわち、本発明は、
(1)(A)基油に、(B)有機物で処理したベントナイト系粘土鉱物有機物で処理したベントナイト系粘土鉱物、及び(C)活性硫黄化合物を含有してなる金属加工油組成物、
(2)(B)の有機物で処理したベントナイト系粘土鉱物が、第四級アンモニウム塩で処理したベントナイト、又はモンモリロナイトである前記(1)に記載の金属加工油組成物、
(3)(C)の活性硫黄化合物がジアルキルポリサルファイド及び/又は硫化油脂である前記(1)又は(2)に記載の金属加工油組成物、
(4)さらに、(D)(i)油脂、(ii)炭素数6〜24の脂肪酸,炭素数12〜40の二塩基酸、及びそれらのエステル化合物、並びに(iii)リン含有化合物から選ばれた少なくとも一種の化合物を含有してなる前記(1)〜(3)のいずれかに記載の金属加工油組成物、
(5)金属加工の被加工材が、鉄系金属材、クロム系金属材、ニッケル系金属材、又はアルミ厚板材である前記(1)〜(4)のいずれかに記載の金属加工油組成物、
(5)金属加工が、絞り加工、切削加工、引抜き加工、鍛造加工、打抜き加工、押抜き加工、ファインブランキング加工、スウェージング加工のいずれかの加工である前記(1)〜(5)のいずれかに記載の金属加工油組成物、
を提供するものである。
That is, the present invention
(1) A metalworking oil composition comprising (A) a base oil, (B) a bentonite clay mineral treated with an organic substance, a bentonite clay mineral treated with an organic substance, and (C) an active sulfur compound,
(2) The metalworking oil composition according to (1), wherein the bentonite clay mineral treated with the organic substance of (B) is bentonite treated with a quaternary ammonium salt or montmorillonite,
(3) The metalworking oil composition according to (1) or (2), wherein the active sulfur compound of (C) is a dialkyl polysulfide and / or a sulfurized fat or oil,
(4) Further, selected from (D) (i) fats and oils, (ii) fatty acids having 6 to 24 carbon atoms, dibasic acids having 12 to 40 carbon atoms, and ester compounds thereof, and (iii) phosphorus-containing compounds. The metalworking oil composition according to any one of (1) to (3), further comprising at least one compound.
(5) The metal processing oil composition according to any one of (1) to (4), wherein the workpiece for metal processing is an iron metal material, a chromium metal material, a nickel metal material, or an aluminum thick plate material. Stuff,
(5) The above (1) to (5), wherein the metal processing is any one of drawing, cutting, drawing, forging, punching, punching, fine blanking, and swaging. The metalworking oil composition according to any one of the above,
Is to provide.

本発明の金属加工油組成物によれば、鉄系金属材、クロム系金属材、ニッケル系金属材、又はアルミ厚板材などの難加工材の加工に対しても優れた加工性を有し、非塩素系加工油であっても、塩素系加工油より優れた加工性を有する金属加工油組成物である。   According to the metalworking oil composition of the present invention, it has excellent workability for processing difficult-to-work materials such as iron-based metal materials, chromium-based metal materials, nickel-based metal materials, or aluminum thick plate materials, Even if it is a non-chlorine type processing oil, it is a metal processing oil composition which has the workability superior to the chlorine type processing oil.

本発明は、(A)基油に、(B)有機物で処理したベントナイト系粘土鉱物、及び(C)活性硫黄化合物を含有してなる金属加工油組成物である。   The present invention is a metalworking oil composition comprising (A) a base oil, (B) a bentonite clay mineral treated with an organic substance, and (C) an active sulfur compound.

本発明の金属加工油組成物を構成する(A)成分の基油としては、特に制限はないが、代表例としては、鉱油,合成油,及び高分子化合物が挙げられる。上記鉱油としては、様々なものを使用することができるが、40℃における動粘度が1〜1000mm2/s、特に、2〜500mm2/sのものが好適に用いられる。動粘度が1mm2/s未満では、引火点が低く、安全上好ましくなく、また、1000mm2/sを超えると、油剤がワーク(被加工物)に付着して持ち去られる量が多くなり、経済的でなくなる場合があり好ましくない。このような鉱油としては、種々のものを挙げることができる。例えば、パラフィン基系原油,中間基系原油あるいはナフテン基系原油を常圧蒸留するか、あるいは常圧蒸留の残渣油を減圧蒸留して得られる留出油、またはこれを常法にしたがって精製することによって得られる精製油、例えば、溶剤精製油,水添精製油,脱ロウ処理油,白土処理油等を挙げることができる。 Although there is no restriction | limiting in particular as a base oil of (A) component which comprises the metalworking oil composition of this invention, Mineral oil, synthetic oil, and a high molecular compound are mentioned as a representative example. Although various things can be used as said mineral oil, The kinematic viscosity in 40 degreeC is 1-1000 mm < 2 > / s, Especially the thing of 2-500 mm < 2 > / s is used suitably. If the kinematic viscosity is less than 1 mm 2 / s, the flash point is low, which is not preferable for safety, and if it exceeds 1000 mm 2 / s, the amount of oil that adheres to the workpiece (workpiece) increases and the economy increases. It is not preferable because it may not be correct. Examples of such mineral oil include various oils. For example, distillate obtained by subjecting paraffin-based crude oil, intermediate-based crude oil, or naphthenic-based crude oil to atmospheric distillation, or distilling oil obtained by subjecting atmospheric distillation residue oil to vacuum distillation, or purifying it according to a conventional method. For example, solvent refined oil, hydrogenated refined oil, dewaxed oil, and clay-treated oil can be used.

また、合成油としては、例えば、炭素数8〜14のポリ−α−オレフィン,オレフィンコポリマー(例えば、エチレン−プロピレンコポリマーなど)、あるいはポリブテン,ポリプロピレン等の分岐オレフィンやこれらの水素化物、さらにはポリオールエステル(トリメチロールプロパンの脂肪酸エステル,ペンタエリスリトールの脂肪酸エステルなど)や二塩基酸エステル等のエステル系化合物、アルキルベンゼン等を用いることができる。   Synthetic oils include, for example, poly-α-olefins having 8 to 14 carbon atoms, olefin copolymers (for example, ethylene-propylene copolymers), branched olefins such as polybutene and polypropylene, hydrides thereof, and polyols. Esters such as esters (fatty acid esters of trimethylolpropane, fatty acid esters of pentaerythritol, etc.), dibasic acid esters, alkylbenzenes, and the like can be used.

また、高分子化合物としては、炭化水素系高分子化合物、又は含酸素系高分子化合物が好ましく、100℃における動粘度が10〜8000mm2/sの範囲にあるものが好ましい。このような高分子化合物としては、例えば、ポリオレフィン、ポリブテン、ポリイソブチレン、ポリアルキレングルコール、ポリメタアクリレート,オレフィンコポリマー(例えば、エチレン−プロピレンコポリマー,スチレン−ブタジエンコポリマー,スチレン−イソプレンコポリマーなど)等が挙げられる。これらの高分子化合物の中でも、ポリオレフィン、ポリブテン、ポリイソブチレンなどの炭化水素系高分子化合物がより好ましい。これらの鉱油,合成油,高分子化合物は、単独で用いてもよく、また複数を混合して用いても良い。また、高分子化合物は、鉱油や合成油と混合して組成物の動粘度を調整するために使用してもよい。 The polymer compound is preferably a hydrocarbon polymer compound or an oxygen-containing polymer compound, and preferably has a kinematic viscosity at 100 ° C. in the range of 10 to 8000 mm 2 / s. Examples of such a polymer compound include polyolefin, polybutene, polyisobutylene, polyalkylene glycol, polymethacrylate, olefin copolymer (for example, ethylene-propylene copolymer, styrene-butadiene copolymer, styrene-isoprene copolymer) and the like. Can be mentioned. Among these polymer compounds, hydrocarbon polymer compounds such as polyolefin, polybutene, and polyisobutylene are more preferable. These mineral oils, synthetic oils, and polymer compounds may be used alone or in combination. Moreover, you may use a high molecular compound in order to mix with mineral oil and synthetic oil, and to adjust the kinematic viscosity of a composition.

本発明の金属加工油組成物においては、(B)成分として有機物で処理したベントナイト系粘土鉱物を用いる。この有機物で処理したベントナイト系粘土鉱物とは、ベントナイト系粘土鉱物の結晶層間に存在する無機陽イオンを有機陽イオンと交換して生成される有機イオン複合体であり、いわゆる、有機ベントナイトを意味する。
ここでいうベントナイト系粘土鉱物とは、ベントナイト、及びベントナイトの主成分であるモンモリロナイトを含んでいる。このようなベントナイト系粘土鉱物は、平均粒径が10μm以下のものが好ましく、8μm以下のものがより好ましい。
In the metalworking oil composition of the present invention, bentonite clay mineral treated with an organic substance is used as the component (B). The bentonite clay mineral treated with this organic substance is an organic ion complex produced by exchanging inorganic cations existing between the crystal layers of bentonite clay minerals with organic cations, meaning so-called organic bentonite. .
The bentonite clay mineral here includes bentonite and montmorillonite which is a main component of bentonite. Such bentonite clay minerals preferably have an average particle size of 10 μm or less, and more preferably 8 μm or less.

上記ベントナイト系粘土鉱物を有機物で処理する、有機陽イオンとしては、アンモニウムイオンが好ましく、特に四級アンモニウムイオンが好ましい。このようなアンモニウムイオンの具体例としては、例えば、テトラエチルアンモニウム、テトラブチルアンモニウム、テトラオクチルアンモニウム等の同一アルキル基を有する第四級アンモニウム、トリメチルオクチルアンモニウム、トリメチルデシルアンモニウム、トリメチルドデシルアンモニウム、トリメチルテトラデシルアンモニウム、トリメチルヘキサデシルアンモニウム、トリメチルオクタデシルアンモニウム、トリメチルエイコサニルアンモニウム、トリメチルオクタデセニルアンモニウム、トリメチルオクタデカジエニルアンモニウム等のトリメチルアルキルアンモニウム、トリエチルドデシルアンモニウム、トリエチルテトラデシルアンモニウム、トリエチルヘキサデシルアンモニウム、トリエチルオクタデシルアンモニウム等のトリエチルアルキルアンモニウム、トリブチルドデシルアンモニウム、トリブチルテトラデシルアンモニウム、トリブチルヘキサデシルアンモニウム、トリブチルオクタデシルアンモニウム等のトリブチルアルキルアンモニウム、ジメチルジオクチルアンモニウム、ジメチルジデシルアンモニウム、ジメチルジテトラデシルアンモニウム、ジメチルジヘキサデシルアンモニウム、ジメチルジオクタデシルアンモニウム、ジメチルジオクタデセニルアンモニウム、ジメチルジオクタデカジエニルアンモニウム等のジメチルジアルキルアンモニウム、ジエチルジドデシルアンモニウム、ジエチルジテトラデシルアンモニウム、ジエチルジヘキサデシルアンモニウム、ジエチルジオクタデシルアンモニウム等のジエチルジアルキルアンモニウム、ジブチルジドデシルアンモニウム、ジブチルジテトラデシルアンモニウム、ジブチルジヘキサデシルアンモニウム、ジブチルジオクタデシルアンモニウム等のジブチルジアルキルアンモニウム、メチルベンジルヘキサデシルアンモニウム等のメチルベンジルジアルキルアンモニウム、ジベンジルジヘキサデシルアンモニウム等のジベンジルジアルキルアンモニウム、トリオクチルメチルアンモニウム、トリドデシルメチルアンモニウム、トリテトラデシルメチルアンモニウム、トリパルミトイルメチルアンモニウム、トリオレイルメチルアンモニウム、トリステアリルメチルアンモニウム等のトリアルキルメチルアンモニウム、トリオクチルエチルアンモニウム、トリドデシルエチルアンモニウム等のトリアルキルエチルアンモニウム、トリオクチルブチルアンモニウム、トリドデシルブチルアンモニウム等のトリアルキルブチルアンモニウム、トリメチルベンジルアンモニウム等の芳香環を有する第四級アンモニウム及びトリメチルフェニルアンモニウム等の芳香族アミン由来の第四級アンモニウムイオン等のイオン類が挙げられる。   The organic cation for treating the bentonite clay mineral with an organic substance is preferably an ammonium ion, particularly preferably a quaternary ammonium ion. Specific examples of such ammonium ions include, for example, quaternary ammonium having the same alkyl group such as tetraethylammonium, tetrabutylammonium, tetraoctylammonium, trimethyloctylammonium, trimethyldecylammonium, trimethyldodecylammonium, trimethyltetradecyl. Ammonium, trimethyl hexadecyl ammonium, trimethyl octadecyl ammonium, trimethyl eicosanyl ammonium, trimethyl octadecenyl ammonium, trimethyl alkyl ammonium such as trimethyl octadecadienyl ammonium, triethyl dodecyl ammonium, triethyl tetradecyl ammonium, triethyl hexadecyl ammonium, Triethyloctadecylammonium Such as triethylalkyl ammonium, tributyl dodecyl ammonium, tributyl tetradecyl ammonium, tributyl hexadecyl ammonium, tributyl octadecyl ammonium, dimethyl dioctyl ammonium, dimethyl didecyl ammonium, dimethyl ditetradecyl ammonium, dimethyl dihexadecyl ammonium, Dimethyldialkylammonium such as dimethyldioctadecylammonium, dimethyldioctadecenylammonium, dimethyldioctadecadienylammonium, diethyldidodecylammonium, diethylditetradecylammonium, diethyldihexadecylammonium, diethyldioctadecylammonium, etc. Dialkylammonium Dibutyl didodecyl ammonium, dibutyl ditetradecyl ammonium, dibutyl dihexadecyl ammonium, dibutyl dialkyl ammonium such as dibutyl dioctadecyl ammonium, methyl benzyl dialkyl ammonium such as methyl benzyl hexadecyl ammonium, dibenzyl such as dibenzyl dihexadecyl ammonium Dialkylammonium, trioctylmethylammonium, tridodecylmethylammonium, tritetradecylmethylammonium, tripalmitoylmethylammonium, trioleylmethylammonium, tristearylmethylammonium, etc. Trialkylmethylammonium, trioctylethylammonium, tridodecylethylammonium, etc. Of trialkylethylammonium Ions such as quaternary ammonium ions such as trialkylbutylammonium such as lyoctylbutylammonium and tridodecylbutylammonium and quaternary ammonium having an aromatic ring such as trimethylbenzylammonium and trimethylphenylammonium Can be mentioned.

(C)成分活性硫黄化合物の存在下で、上記のようなベントナイト系粘土鉱物を配合することにより、加工性を高めることができる。また有機物で処理したことによって、基油に対し安定して分散し、その配合効果を安定して発揮することができる。
これらの有機物で処理したベントナイト系粘土鉱物は、一種を単独で配合してもよいが、二種以上を組み合わせて配合しても良い。
かかる有機物で処理したベントナイト系粘土鉱物の配合量については、組成物を基準にして、0.5〜10質量%の範囲が好ましく、その範囲内で加工の程度(厳しさ)に応じて適宜選定すればよい。例えば、絞り、プレスや打抜き、冷間鍛像加工等に使用する40℃における動粘度がおよそ、20〜500mm2/sの低粘度油の場合は0.5〜3質量%程度、また、引抜き、押し抜き加工等に使用される40℃における動粘度がおよそ500mm2/s以上の高粘度油では3〜10質量%程度配合するのが好ましい。
(C) Component In the presence of an active sulfur compound, workability can be improved by blending the bentonite clay mineral as described above. Moreover, by processing with organic substance, it can disperse | distribute stably with respect to base oil, and can show the compounding effect stably.
The bentonite clay mineral treated with these organic substances may be blended alone or in combination of two or more.
About the compounding quantity of the bentonite-type clay mineral processed with this organic substance, the range of 0.5-10 mass% is preferable on the basis of a composition, and it selects suitably according to the grade (severity) of processing within the range. do it. For example, in the case of a low-viscosity oil having a kinematic viscosity at 40 ° C. of about 20 to 500 mm 2 / s used for drawing, pressing and punching, cold forging, etc., about 0.5 to 3% by mass, In a high viscosity oil having a kinematic viscosity at 40 ° C. of about 500 mm 2 / s or more used for punching or the like, about 3 to 10% by mass is preferably blended.

次に、本発明の金属加工油組成物を構成する(C)成分としての活性硫黄化合物とは、活性硫黄を含有するためにJIS K 2513に規定する銅板腐食試験において「3」以上の判定結果を示す化合物をいう。活性硫黄化合物でなく、不活性な硫黄化合物であると、加工性を向上させることができず、(C)成分としては不適当である。
本発明で使用される活性硫黄化合物としては、例えば、オレフィンポリサルファイド,ジアルキルポリサルファイド,硫化油脂,または硫化鉱油もしくは単体硫黄(硫黄粉末)などが挙げられる。
Next, the active sulfur compound as the component (C) constituting the metalworking oil composition of the present invention is a judgment result of “3” or more in the copper plate corrosion test specified in JIS K 2513 because it contains active sulfur. The compound which shows this. If it is not an active sulfur compound but an inert sulfur compound, the processability cannot be improved, and it is inappropriate as the component (C).
Examples of the active sulfur compound used in the present invention include olefin polysulfide, dialkyl polysulfide, sulfurized fat and oil, sulfide mineral oil, or elemental sulfur (sulfur powder).

上記オレフィンポリサルファイドは、様々な方法によって製造することができるが、例えば、炭素数3〜20のオレフィン又はその2〜4量体と硫化剤とを反応させることによって得られるものである。ここで、炭素数3〜20のオレフィンとしては、例えば、プロピレン,イソブテン,ジイソブテンなどが好ましく用いられる。一方、硫化剤としては、例えば、硫黄,塩化硫黄,ハロゲン化硫黄などが挙げられる。上記反応によって得られるオレフィンポリサルファイドのイオウ含有量としては、通常、10〜50質量%のものが、溶解性,安定性,経済性の点で望ましい。   The olefin polysulfide can be produced by various methods. For example, the olefin polysulfide is obtained by reacting an olefin having 3 to 20 carbon atoms or a dimer or tetramer thereof with a sulfurizing agent. Here, as a C3-C20 olefin, propylene, isobutene, diisobutene etc. are used preferably, for example. On the other hand, examples of the sulfurizing agent include sulfur, sulfur chloride, sulfur halide and the like. The sulfur content of the olefin polysulfide obtained by the above reaction is usually preferably 10 to 50% by mass in terms of solubility, stability and economy.

また、ジアルキルポリサルファイドは、例えば一般式(I)   In addition, dialkyl polysulfide is, for example, represented by the general formula (I)

Figure 2005314558
Figure 2005314558

〔式中、R1 及びR2 は、それぞれ炭素数1〜20のアルキル基、炭素数6〜20のアリール基、炭素数7〜20のアルキルアリール基又は炭素数7〜20のアリールアルキル基を示し、それらは互いに同一でも異なっていてもよい。xは2〜8の実数(詳しくは有理数)を示す。〕で表される化合物である。上記一般式(I) におけるR1 及びR2 の具体例としては、メチル基,エチル基,n−プロピル基,イソプロピル基,n−ブチル基,イソブチル基,sec−ブチル基,t−ブチル基,各種ペンチル基,各種ヘキシル基,各種ヘプチル基,各種オクチル基,各種ノニル基,各種デシル基,各種ドデシル基,シクロヘキシル基,シクロオクチル基,フェニル基,ナフチル基,トリル基,キシリル基,ベンジル基,フェネチル基などが挙げられる。
このジアルキルポリサルファイドとしては、xが3〜6、R1,R2が炭素数16〜20アルキル基、6〜20のアリール基である化合物が好ましい。具体的には、例えば、ジベンジルジサルファイドやジ−t−ノニルポリサルファイドなどが挙げられ、特に、硫黄を10〜50質量%含有するものが好適である。
Wherein, R 1 and R 2 are each an alkyl group having 1 to 20 carbon atoms, an aryl group having 6 to 20 carbon atoms, an alkylaryl group or an arylalkyl group having 7 to 20 carbon atoms of 7 to 20 carbon atoms They may be the same or different from each other. x represents a real number (more specifically, a rational number) of 2 to 8. It is a compound represented by this. Specific examples of R 1 and R 2 in the general formula (I) include methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, isobutyl group, sec-butyl group, t-butyl group, Various pentyl groups, various hexyl groups, various heptyl groups, various octyl groups, various nonyl groups, various decyl groups, various dodecyl groups, cyclohexyl groups, cyclooctyl groups, phenyl groups, naphthyl groups, tolyl groups, xylyl groups, benzyl groups, Examples thereof include a phenethyl group.
The dialkyl polysulfide is preferably a compound in which x is 3 to 6, R 1 and R 2 are an alkyl group having 16 to 20 carbon atoms and an aryl group having 6 to 20 carbon atoms. Specific examples include dibenzyl disulfide and di-t-nonyl polysulfide, and those containing 10 to 50% by mass of sulfur are particularly suitable.

前記の硫化油脂は、動植物油の硫化物を指し、例えば、硫化ラード,硫化なたね油,硫化ひまし油,硫化大豆油などがある。また、この硫化油脂は、硫化オレイン酸などの二硫化脂肪酸、硫化オレイン酸メチルなどの硫化エステルも包含する。該硫化油脂としては、硫黄分を5〜30質量%含有するものが好適である。
また、前記の硫化鉱油もしくは単体硫黄としては、市販の硫化鉱油を使用してもよく、あるいは、通常の鉱油に単体硫黄(硫黄粉末)を加え、例えば、120〜150℃程度の温度で、30分〜6時間程度加熱、攪拌して調製したものを用いてもよい。この硫化鉱油は、硫黄を0.1〜2質量%含有するものが好適である。
The sulfurized fats and oils refer to sulfides of animal and vegetable oils, and examples thereof include sulfurized lard, sulfurized rapeseed oil, sulfurized castor oil, and sulfurized soybean oil. The sulfurized fats and oils also include disulfide fatty acids such as sulfurized oleic acid and sulfurized esters such as methyl sulfurized oleate. As this sulfurized oil and fat, what contains 5-30 mass% of sulfur content is suitable.
Moreover, as said sulfide mineral oil or simple substance sulfur, you may use a commercially available sulfide mineral oil, or add simple sulfur (sulfur powder) to normal mineral oil, for example, at the temperature of about 120-150 degreeC, 30 You may use what was prepared by heating and stirring for about minutes to 6 hours. The sulfide mineral oil preferably contains 0.1 to 2% by mass of sulfur.

本発明においては、上記各種の活性硫黄化合物のうち、ジアルキルポリサルファイドが好ましく、中でも、効果、及び入手性の観点から、ジオクチルポリサルファイド、ジドデシルポリサルファイドなどが好ましい。
また、これら活性硫黄化合物は、一種を単独で配合してもよいが、二種以上を組み合わせて配合しても良い。
上記(C)成分の活性硫黄を含有する化合物の配合量は、特に制限はないが、硫黄分が、組成物を基準にして1〜30質量%となるように配合することが好ましい。この範囲であれば、目的の加工性が得られ、金型や工具の摩耗の進行などの不都合を抑制できる。また、活性硫黄化合物とは、硫黄含有量が異なるため、選択された硫黄化合物に応じて変動するが、通常、組成物を基準にして5〜70質量%が好ましく、15〜60質量%がより好ましい。
In the present invention, among the above various active sulfur compounds, dialkyl polysulfide is preferable, and among them, dioctyl polysulfide, didodecyl polysulfide, and the like are preferable from the viewpoints of effects and availability.
These active sulfur compounds may be blended alone or in combination of two or more.
Although the compounding quantity of the compound containing the active sulfur of the said (C) component does not have a restriction | limiting in particular, It is preferable to mix | blend so that a sulfur content may be 1-30 mass% on the basis of a composition. If it is this range, the target workability will be acquired and inconveniences, such as progress of abrasion of a metal mold | die and a tool, can be suppressed. In addition, since the sulfur content is different from the active sulfur compound, it varies depending on the selected sulfur compound, but is usually preferably 5 to 70% by mass, more preferably 15 to 60% by mass based on the composition. preferable.

本発明の金属加工油組成物は、さらに(D)成分として(i)油脂、(ii)炭素数6〜24の脂肪酸,炭素数12〜40の二塩基酸、及びそれらのエステル化合物、並びに(iii)リン含有化合物から選ばれた少なくとも一種を配合することが好ましい。これによって、さらに加工性を高めることができる。
ここでいう(i)油脂としては、例えば、大豆油、あまに油、なたね油等の植物油、牛脂、ラード等の動物油などを挙げることができる。また、(ii)炭素数6〜24の脂肪酸としては、特に制限はないが、代表例としてオレイン酸、ステアりん酸などがあげられる。また炭素数12〜40の二塩基酸としては、公知の種々のものが使用でき、代表例としては、アジピン酸、セバシン酸、1,8−ジカルボキシオクタン、1,20−ジカルボキシエイコサン、などが挙げられる。
また、それらのエステル化合物としては、それらの脂肪酸や二塩基酸と炭素数1〜24のアルコール類とのエステルが好ましく、例えば,アジピン酸ジブチル, アジピン酸ジ−2−エチルヘキシル、セバシン酸ジ−2−エチルヘキシルなどが挙げられる。
The metalworking oil composition of the present invention further comprises (i) an oil, (ii) a fatty acid having 6 to 24 carbon atoms, a dibasic acid having 12 to 40 carbon atoms, and an ester compound thereof, as (D) component; iii) It is preferable to blend at least one selected from phosphorus-containing compounds. Thereby, workability can be further improved.
Examples of the (i) fats and oils herein include vegetable oils such as soybean oil, sesame oil and rapeseed oil, and animal oils such as beef tallow and lard. Further, (ii) the fatty acid having 6 to 24 carbon atoms is not particularly limited, but representative examples include oleic acid and stearic acid. As the dibasic acid having 12 to 40 carbon atoms, various known ones can be used. Typical examples include adipic acid, sebacic acid, 1,8-dicarboxyoctane, 1,20-dicarboxyeicosane, Etc.
The ester compounds are preferably esters of these fatty acids or dibasic acids and alcohols having 1 to 24 carbon atoms, such as dibutyl adipate, di-2-ethylhexyl adipate, di-2 sebacate. -Ethylhexyl and the like.

次に(iii)リン含有化合物としては、アルキルフォスフェート、ハイドロジェンフォスファイト及びそれらのアミン塩、ジンクジチオフォスフェートが或いはモリブデンジチオフォスフェートをいい、それぞれ公知化合物を使用できる。これらのリン含有化合物の中で、特に好ましい化合物としては、ジラウリルハイドロジェンフォスファイト、トリノニルフォスファイト、オレイルアシッドフォスフェート、トリオレイルフォスフェート、2−エチルヘキシルアシッドフォスフェートの牛脂アミン塩、ジンクジチオフォスフェート、及びモリブデンジチオフォスフェートなどが挙げられる。
これらのリン含有化合物は、一種を単独で配合してもよいが、二種以上を組み合わせて配合しても良い。
このようなリン含有化合物の配合量は、0.1〜10質量%が好ましく、0.5〜8質量%がより好ましい。リン含有化合物の配合量は、0.1〜10質量%であれば、加工性の向上の目的が達せられ、また、金型や工具が摩耗する恐れもない。
Next, as (iii) phosphorus-containing compounds, alkyl phosphates, hydrogen phosphites and their amine salts, zinc dithiophosphates or molybdenum dithiophosphates are used, and known compounds can be used respectively. Among these phosphorus-containing compounds, particularly preferred compounds are dilauryl hydrogen phosphite, trinonyl phosphite, oleyl acid phosphate, trioleyl phosphate, 2-ethylhexyl acid phosphate beef tallow amine salt, zinc dike Examples thereof include thiophosphate and molybdenum dithiophosphate.
These phosphorus-containing compounds may be blended singly or in combination of two or more.
0.1-10 mass% is preferable and the compounding quantity of such a phosphorus containing compound has more preferable 0.5-8 mass%. If the compounding quantity of a phosphorus containing compound is 0.1-10 mass%, the objective of the workability improvement will be achieved and there is also no possibility that a metal mold | die and a tool will be worn out.

本発明の金属加工油組成物においては、さらに本発明の目的に反しない範囲で公知の添加剤を配合できる。そのような添加剤としては、例えば、フェノール系、アミン系などの酸化防止剤、ベンゾトリアゾール系、チアゾール系などの腐食防止剤、金属スルホネート系、こはく酸エステル系などの錆止め剤、シリコン系、フッ素化シリコン系などの消泡剤、ポリメタアクリレート系、オレフィンコーポリマー系などの粘度指数向上剤などが挙げられる。これらの添加剤の配合量は、目的に応じて適宜選定すればよいが、通常これらの添加剤の合計が組成物を基準にして20質量%以下になるように配合する。
本発明の金属加工油組成物の動粘度については、特に制限はないが、およそ20〜20000mm2/sの範囲にあるものが好ましい。金属加工油組成物の動粘度がおよそ20〜20000mm2/sの範囲であれば、加工性が良好で、引火性などの面からも安全性が確保でき、油剤が被加工物に付着して持ち去られる量の面ついても、経済的に問題がない。
上記の本発明の金属加工油組成物は、あらゆる金属加工について使用できるが、鉄系金属材、クロム系金属材、ニッケル系金属材、又はアルミ厚板材などの難加工材の加工に対しても使用できる。また、本発明の金属加工油組成物を用いる金属加工方法の種類については、特に制限はなく、例えば、絞り加工、切削加工、引抜き加工、鍛造加工、打抜き加工、押抜き加工、ファインブランキング加工、スウェージング加工などに利用できる。
In the metalworking oil composition of the present invention, a known additive can be further blended within a range not contrary to the object of the present invention. Examples of such additives include antioxidants such as phenols and amines, corrosion inhibitors such as benzotriazoles and thiazoles, rust inhibitors such as metal sulfonates and succinates, silicons, fluorine Examples thereof include antifoaming agents such as silicon fluoride, and viscosity index improvers such as polymethacrylate and olefin copolymer. The blending amount of these additives may be appropriately selected according to the purpose, but is usually blended so that the total of these additives is 20% by mass or less based on the composition.
Although there is no restriction | limiting in particular about the kinematic viscosity of the metalworking oil composition of this invention, What is in the range of about 20-20000 mm < 2 > / s is preferable. If the kinematic viscosity of the metalworking oil composition is in the range of about 20 to 20000 mm 2 / s, the workability is good and safety can be secured from the standpoint of flammability, and the oil agent adheres to the workpiece. There is no economic problem in terms of the amount taken away.
The metal processing oil composition of the present invention can be used for all types of metal processing, but also for processing difficult-to-process materials such as iron-based metal materials, chromium-based metal materials, nickel-based metal materials, and aluminum thick plate materials. Can be used. Moreover, there is no restriction | limiting in particular about the kind of metal processing method using the metalworking oil composition of this invention, For example, drawing, cutting, drawing, forging, punching, punching, fine blanking Can be used for swaging, etc.

次に、本発明を実施例により、さらに詳細に説明するが、本発明は、この例によってなんら限定されるものではない。
(評価方法)
各実施例及び比較例で得られた試料油について、以下の方法で評価した。
(1)円筒絞り実験
以下の条件で円筒絞り実験を行った。
実験機:JTトーシ製深絞り試験機
板材質:SUS304 (Φ70mm、厚さ0.8mm)
ポンチ:SKD11(φ32.0mm、肩R=5mm)
ダイス:SKD11(φ34.8mm、肩R=5mm)
シワ押え力:0.4t
絞り深さ:20mm
絞り深さ:10mm/s
評価項目:
板を20枚加工したときの、ポンチ荷重を測定し、工具と板の表面状態を観 察し、摩耗やキズの発生の有無を調べた。
(2)断続切削実験
以下の条件で断続切削条実験を行った。この実験は、ファインブランキング加工性も評価できる。
ワーク :SKD11,φ81,8スリット
工具 :超硬
切削速度v:50m/min(200rpm)
切込みt :1mm,送りf=1μm/rev
切削長L :5mm×5回繰り返し
合計パス回数:5mm×5回×8スリット÷0.001mm=20万パス(フ ァインブランキング20万ショット相当)
評価項目 :送り分力(加工安定性)、及び工具摩耗を観察した。
EXAMPLES Next, although an Example demonstrates this invention further in detail, this invention is not limited at all by this example.
(Evaluation methods)
The sample oil obtained in each example and comparative example was evaluated by the following method.
(1) Cylindrical drawing experiment A cylindrical drawing experiment was performed under the following conditions.
Experimental machine: JT Toshi deep drawing tester Plate material: SUS304 (Φ70mm, thickness 0.8mm)
Punch: SKD11 (φ32.0mm, shoulder R = 5mm)
Dice: SKD11 (φ34.8mm, shoulder R = 5mm)
Wrinkle presser force: 0.4t
Drawing depth: 20mm
Drawing depth: 10mm / s
Evaluation item:
When 20 sheets were machined, the punch load was measured, the surface condition of the tool and the board was observed, and the presence or absence of wear and scratches was examined.
(2) Intermittent cutting experiment An intermittent cutting strip experiment was performed under the following conditions. This experiment can also evaluate fine blanking workability.
Workpiece: SKD11, φ81, 8 slit Tool: Carbide Cutting speed v: 50 m / min (200 rpm)
Cutting depth t: 1 mm, feed f = 1 μm / rev
Cutting length L: Repeated 5 mm x 5 times Total number of passes: 5 mm x 5 times x 8 slits ÷ 0.001 mm = 200,000 passes (Fine blanking equivalent to 200,000 shots)
Evaluation items: Feed force (machining stability) and tool wear were observed.

(3)平板引抜き実験
以下の条件で平板引抜き実験を行った。
試験機:インストロン試験機
減面率:7.2%
摺動速度:200mm/s
試験温度:22℃
引抜き距離:150mm
試験片(板):SUS304(10 mm x 300mm x 4 mm)
ポンチ:WC (1R)
評価項目:平均引抜き抵抗を比較
(4)冷間鍛造実験
以下の条件で冷間鍛造実験を行った。
試験機:SAKAMURA NP−450H
段数:4段打
加工速度:150個/分
テストピース:6角フランジナット製造用S−45C(φ19mm×9.5×10mm)
パンチ及びダイス材質:SKH、SKD
(3) Flat plate extraction experiment A flat plate extraction experiment was performed under the following conditions.
Testing machine: Instron testing machine Area reduction rate: 7.2%
Sliding speed: 200mm / s
Test temperature: 22 ° C
Pull-out distance: 150mm
Test piece (plate): SUS304 (10 mm x 300 mm x 4 mm)
Punch: WC (1R)
Evaluation item: Comparison of average drawing resistance (4) Cold forging experiment A cold forging experiment was performed under the following conditions.
Testing machine: SAKAMURA NP-450H
Number of steps: 4 steps Processing speed: 150 pieces / minute Test piece: S-45C for hexagonal flange nut production (φ19mm × 9.5 × 10mm)
Punch and die material: SKH, SKD

(試料油及び比較油)
比較油−1
市販の塩素系絞り油(40℃の動粘度が29mm2/s、塩素含有量18.6質量%)
比較油−2
市販の非塩素系絞り油(40℃の動粘度が78mm2/s、硫黄含有量2.6質量%)
比較油−3
40℃の動粘度が9.5mm2/s のナフテン系鉱油40質量%、活性硫黄系ポリサルファイド(大日本インキ製ダイルーブS940)40質量%、リン系化合物(Vanderbilt製VANLUBE 672)18質量%、有機物処理をしていないベントナイト(ホージュン製ベンゲルHVP)2質量%を混合し、見かけ40℃の動粘度が46mm2/s の油剤を調整した。
比較油−4
市販の塩素系引抜油(40℃の動粘度が17600mm2/s 、塩素含有量28.3質量%)
(Sample oil and comparative oil)
Comparative oil-1
Commercially available chlorinated squeezed oil (kinematic viscosity at 40 ° C. is 29 mm 2 / s, chlorine content is 18.6% by mass)
Comparative oil-2
Commercially available non-chlorinated squeezed oil (kinematic viscosity at 40 ° C is 78 mm 2 / s, sulfur content 2.6 mass%)
Comparative oil-3
40% by mass of naphthenic mineral oil having a kinematic viscosity at 40 ° C. of 9.5 mm 2 / s, 40% by mass of active sulfur-based polysulfide (Dairubu S940 made by Dainippon Ink), 18% by mass of phosphorus compound (VANLUBE 672 manufactured by Vanderbilt), organic matter Untreated bentonite (Hojung Bengel HVP) 2% by mass was mixed to prepare an oil agent having an apparent kinematic viscosity of 40 ° C. and 46 mm 2 / s.
Comparative oil-4
Commercially available chlorine-based drawn oil (kinematic viscosity at 40 ° C is 17600 mm 2 / s, chlorine content is 28.3 mass%)

試料油−1
40℃の動粘度が9.5mm2/s のナフテン系鉱油40質量%、活性硫黄系ポリサルファイド(大日本インキ製ダイルーブS940)40質量%、リン系化合物(Vanderbilt製VANLUBE 672)18質量%、第四級アンモニウムで処理したベントナイト(ホージュン製S−BEN NZ)2質量%を混合し、硫黄含有量13.2質量%、40℃の動粘度が46mm2/sの油剤を調整した。混合は、先ずナフテン系鉱油と表面修飾ベントナイトを100℃、350rpmで1時間攪拌混合し、次いで残りの基材を活性硫黄系ポリサルファイド、リン系化合物の順に100℃の温度を維持しながら順次混合した。
試料油−2
40℃の動粘度が30mm2/sのナフテン系鉱油30質量%、40℃の動粘度が100mm2/sのナフテン系鉱油20質量%、活性硫黄系ポリサルファイド(大日本インキ製ダイルーブS940)43質量%、ジンクジチオフォスフェート(OLONITE製OLOA 260)5質量%、第四級アンモニウムで処理したベントナイト(ホージュン製S−BEN NZ)2質量%を混合し、40℃の動粘度が78mm2/sの油剤を調整した。
Sample oil-1
40% by mass of naphthenic mineral oil having a kinematic viscosity at 40 ° C. of 9.5 mm 2 / s, 40% by mass of active sulfur-based polysulfide (Dairubu S940 manufactured by Dainippon Ink), 18% by mass of phosphorus compound (VANLUBE 672 manufactured by Vanderbilt), No. 1 Bentonite (S-BEN NZ made by Hojun) 2% by mass treated with quaternary ammonium was mixed to prepare an oil agent having a sulfur content of 13.2% by mass and a kinematic viscosity at 40 ° C. of 46 mm 2 / s. First, naphthenic mineral oil and surface-modified bentonite were stirred and mixed at 100 ° C. and 350 rpm for 1 hour, and then the remaining base materials were sequentially mixed while maintaining the temperature of 100 ° C. in the order of active sulfur polysulfide and phosphorus compound. .
Sample oil-2
Naphthenic mineral oil 30 wt% of kinematic viscosity of 40 ° C. is 30mm 2 / s, 40 ℃ naphthenic mineral oil 20 wt% of kinematic viscosity of 100 mm 2 / s, the active sulfur-polysulfide (Dainippon Ink Dairubu S940) 43 Weight %, Zinc dithiophosphate (OLONITE OLOA 260) 5% by mass, bentonite treated with quaternary ammonium (Hojun S-BEN NZ) 2% by mass, 40 ° C. kinematic viscosity 78 mm 2 / s The oil was adjusted.

試料油−3
100℃の動粘度が4300mm2/sのポリブテン43質量%(出光石油化学製20000H)、活性硫黄系ポリサルファイド(大日本インキ製ダイルーブS940)40質量%、炭素数22の二塩基酸(岡村製油製 IPU−22)6質量%、第第四級アンモニウムで処理したベントナイト(ホージュン製S−BEN NZ)8質量%、増粘剤(三洋化成工業製アクルーブ915)3質量%を混合し、40℃の動粘度が13000mm2/sの引抜き専用油剤を調整した。
Sample oil-3
Polybutene with a kinematic viscosity at 100 ° C. of 4300 mm 2 / s 43 mass% (Idemitsu Petrochemical 20000H), active sulfur polysulfide (Dailuo Ink Die-Lube S940) 40 mass%, C22 dibasic acid (Okamura Oil) IPU-22) 6% by mass, bentonite treated with quaternary ammonium (Hojun S-BEN NZ) 8% by mass, thickener (Sanyo Chemical Industries Inc. 915) 3% by mass were mixed, and 40 ° C. A drawing-only oil agent having a kinematic viscosity of 13000 mm 2 / s was prepared.

試料油−4
試料油−1の硫黄系化合物を硫化ラード(大日本インキ製SULFURIZED LARD)40質量%に変更し、硫黄含有量5.6質量%、40℃の動粘度が52mm2/sの油剤を調整した。
試料油−5
試料油−1の硫黄系化合物を硫化油脂(日本ルブリゾール製ANGLAMOL 81)30質量%に変更し、硫黄含有量9.8wt%、40℃の動粘度が64mm2/sの油剤を調整した。
Sample oil-4
The sulfur-based compound of Sample Oil-1 was changed to 40% by mass of sulfurized lard (Dainippon Ink SULFURIZED LARD) to prepare an oil agent having a sulfur content of 5.6% by mass and a kinematic viscosity at 40 ° C. of 52 mm 2 / s. .
Sample oil-5
The sulfur-based compound of Sample Oil-1 was changed to 30% by mass of sulfurized oil (ANGLAMOL 81 manufactured by Nippon Lubrizol), and an oil agent having a sulfur content of 9.8 wt% and a kinematic viscosity at 40 ° C. of 64 mm 2 / s was prepared.

試料油−6
試料油−1のリン系化合物をオレイン酸メチル(日本油脂製ユニスターM−182A)18質量%に変更し、硫黄含有量12.8wt%、40℃の動粘度が37mm2/sの油剤を調整した。
試料油−7
試料油−1のリン系化合物を菜種油(サミット製油製ハイエルシン菜種白絞油)18質量%に変更し、硫黄含有量13.1質量%、40℃の動粘度が42mm2/sの油剤を調整した。
試料油−8
試料油−1のリン系化合物をセバシン酸ジ2エチルヘキシル(三建化工製DOS)18質量%に変更し、硫黄含有量12.6wt%、40℃の動粘度が45mm2/sの油剤を調整した。
試料油−9
40℃の動粘度が9.5mm2/sのナフテン系鉱油41.5質量%、活性硫黄系ポリサルファイド(大日本インキ製ダイルーブS940)40質量%、セバシン酸ジ2エチルヘキシル(三建化工製DOS)18質量%、第四級アンモニウムで処理したベントナイト(ホージュン製S−BEN NZ)0.5質量%を混合し、硫黄含有量12.8wt%、40℃の動粘度が54mm2/sの油剤を調整した。
Sample oil-6
The phosphorus compound of sample oil-1 was changed to 18% by mass of methyl oleate (Nistar M-182A manufactured by NOF Corporation), and an oil agent with a sulfur content of 12.8 wt% and a kinematic viscosity at 40 ° C. of 37 mm 2 / s was prepared. did.
Sample oil-7
The phosphorus-based compounds of the sample oil -1 Change rapeseed oil (Summit OIL CHEMICALS Haierushin rapeseed white refined oil) 18 wt%, a sulfur content of 13.1 wt%, a kinematic viscosity of 40 ° C. to adjust the oil of 42mm 2 / s did.
Sample oil-8
The phosphorus compound of sample oil-1 was changed to 18% by mass of di-2-ethylhexyl sebacate (DOSE, manufactured by Sanken Chemical Co., Ltd.), and an oil agent having a sulfur content of 12.6 wt% and a kinematic viscosity at 40 ° C. of 45 mm 2 / s was prepared. did.
Sample oil-9
41.5% by mass of naphthenic mineral oil having a kinematic viscosity at 40 ° C. of 9.5 mm 2 / s, 40% by mass of active sulfur-based polysulfide (Dairubu S940 made by Dainippon Ink), di-2-ethylhexyl sebacate (DOSE, Sanken Chemical) 18% by mass and 0.5% by mass of bentonite (Hojun S-BEN NZ) treated with quaternary ammonium were mixed, and an oil agent having a sulfur content of 12.8 wt% and a kinematic viscosity at 40 ° C. of 54 mm 2 / s. It was adjusted.

実施例1
試料油−1、4〜8及び比較油1〜3について、(1)の円筒絞り実験を行った。その結果を第1表に示す。
Example 1
A cylindrical squeeze experiment of (1) was performed for sample oils 1, 4 to 8 and comparative oils 1 to 3. The results are shown in Table 1.

Figure 2005314558
Figure 2005314558

第1表によれば、試料油−1,及び4〜8はいずれも比較油−1の塩素系加工油に劣らず、20枚の板を加工をしても、ポンチ荷重は低く安定しており、試験片および工具に摩耗、キズの発生が無く、優れた加工性を示した。
これに対し、比較油―2は、工具に摩耗、キズの発生が無かったが、開始直後から試験片に縦キズが発生し、最終的に無数の大小の縦キズが観察された。比較油―3は、分散状態が不安定で静置により容易に沈殿を生じた。深絞り加工の一枚目で、表面状態にむらが生じた
実施例2
試料油−2と比較油−1について、(2)の断続切削実験を行った。
(実験結果):
工具摩耗については、比較油−1が、110000パスを超えたところから、送り分力が150Nに達し、工具刃先が摩耗状態にあることが確認できたのに対し、試料油−2は、200000パスまで送り分力が120Nと低かった。
また、実験後の工具刃先の摩耗面積については、試料油−2の場合は、比較油−1の場合の2/3であった。
このことより、試料油−2は、比較油−1(塩素系油剤)より安定した切削が可能であり、工具摩耗も少ないことが分かった。また、この結果は、試料油−2が切削油、及び打抜き油として優れていることを示している。
According to Table 1, the sample oils 1 and 4 to 8 are all inferior to the chlorine-based processing oil of the comparative oil-1, and the punch load is low and stable even if 20 plates are processed. The test piece and tool were free from wear and scratches and exhibited excellent workability.
In contrast, Comparative Oil-2 showed no wear or scratches on the tool, but vertical scratches occurred on the specimen immediately after the start, and innumerable large and small vertical scratches were finally observed. Comparative Oil-3 was unstable in dispersion and easily precipitated upon standing. The first surface of the deep drawing was uneven in surface condition.
Example 2
For sample oil-2 and comparative oil-1, the intermittent cutting experiment of (2) was performed.
(Experimental result):
Regarding tool wear, the comparison oil-1 exceeded 110,000 passes, the feed force reached 150 N, and it was confirmed that the tool edge was in a worn state, whereas sample oil-2 was 200000. The feed force to the pass was as low as 120N.
Further, the wear area of the tool edge after the experiment was 2/3 in the case of the sample oil-2 and that in the case of the comparative oil-1.
From this, it was found that Sample Oil-2 can be cut more stably than Comparative Oil-1 (chlorine-based oil) and has less tool wear. Moreover, this result has shown that the sample oil-2 is excellent as cutting oil and punching oil.

実施例3
試料油−3と比較油−4について、(3)の平板引抜き実験を行った。その結果を第2表に示す。
Example 3
For sample oil-3 and comparative oil-4, the flat plate drawing experiment of (3) was performed. The results are shown in Table 2.

Figure 2005314558
Figure 2005314558

試料油−3は、いずれの材質の場合もかじりやキズの発生もなく、第2表によれば、殆どの材料で比較油−4(塩素系油剤)より低い引抜き力で加工が可能である。
実施例4
試料油−9と比較油−2について、(4)の冷間鍛造実験を行った。その結果、比較油−2の硫黄系金属加工油が3万個で工具摩耗が著しく観察され、金型交換を余儀なくされたのに対し、本願発明に係る試料油−9では10万5千個の加工が可能であった。
Sample oil-3 does not cause any galling or scratches in any material, and according to Table 2, it can be processed with a pulling force lower than that of comparative oil-4 (chlorine oil) according to Table 2. .
Example 4
For sample oil-9 and comparative oil-2, the cold forging experiment of (4) was conducted. As a result, tool wear was remarkably observed with 30,000 sulfur-based metalworking oils of comparative oil-2, and the mold was forced to be replaced, whereas sample oil-9 according to the present invention had 105,000. Was possible.

本発明の金属加工油組成物は、鉄系金属材、クロム系金属材、ニッケル系金属材、又はアルミ厚板材などの難加工材の加工に対しても優れた加工性を有し、非塩素系加工油であっても、塩素系加工油より優れた加工性を有する金属加工油組成物である。

The metalworking oil composition of the present invention has excellent workability even for difficult-to-work materials such as iron-based metal materials, chromium-based metal materials, nickel-based metal materials, and aluminum thick plate materials, and is non-chlorine. Even a metal processing oil is a metal processing oil composition having processability superior to that of a chlorine processing oil.

Claims (6)

(A)基油に、(B)有機物で処理したベントナイト系粘土鉱物、及び(C)活性硫黄化合物を含有してなる金属加工油組成物。 A metalworking oil composition comprising (A) a base oil containing (B) a bentonite clay mineral treated with an organic substance and (C) an active sulfur compound. (B)の有機物で処理したベントナイト系粘土鉱物が、第四級アンモニウム塩で処理したベントナイト、又はモンモリロナイトである請求項1に記載の金属加工油組成物。 The metalworking oil composition according to claim 1, wherein the bentonite clay mineral treated with the organic substance (B) is bentonite treated with a quaternary ammonium salt or montmorillonite. (C)の活性硫黄化合物がジアルキルポリサルファイド及び/又は硫化油脂である請求項1又は2に記載の金属加工油組成物。 The metalworking oil composition according to claim 1 or 2, wherein the active sulfur compound (C) is a dialkyl polysulfide and / or a sulfurized fat. さらに、(D)(i)油脂、(ii)炭素数6〜24の脂肪酸,炭素数12〜40の二塩基酸、及びそれらのエステル化合物、並びに(iii)リン含有化合物から選ばれた少なくとも一種の化合物を含有してなる請求項1〜3のいずれかに記載の金属加工油組成物。 Furthermore, at least one selected from (D) (i) fats and oils, (ii) fatty acids having 6 to 24 carbon atoms, dibasic acids having 12 to 40 carbon atoms, and ester compounds thereof, and (iii) phosphorus-containing compounds The metalworking oil composition according to any one of claims 1 to 3, wherein the metal processing oil composition is contained. 金属加工の被加工材が、鉄系金属材、クロム系金属材、ニッケル系金属材、又はアルミ厚板材である請求項1〜4のいずれかに記載の金属加工油組成物。 The metalworking oil composition according to any one of claims 1 to 4, wherein the metalworking material is an iron-based metal material, a chromium-based metal material, a nickel-based metal material, or an aluminum thick plate material. 金属加工が、絞り加工、切削加工、引抜き加工、鍛造加工、打抜き加工、押抜き加工、ファインブランキング加工、スウェージング加工のいずれかの加工である請求項1〜5のいずれかに記載の金属加工油組成物。

The metal according to any one of claims 1 to 5, wherein the metal processing is any one of drawing, cutting, drawing, forging, punching, punching, fine blanking, and swaging. Processing oil composition.

JP2004134470A 2004-04-28 2004-04-28 Metalworking oil composition Expired - Fee Related JP4769426B2 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
JP2004134470A JP4769426B2 (en) 2004-04-28 2004-04-28 Metalworking oil composition
CN2005800127410A CN1946834B (en) 2004-04-28 2005-04-28 metalworking oil composition
PCT/JP2005/008139 WO2005105962A1 (en) 2004-04-28 2005-04-28 Metalworking fluid composition
TW094114108A TW200609345A (en) 2004-04-28 2005-04-28 Oil composition for metalworking

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2004134470A JP4769426B2 (en) 2004-04-28 2004-04-28 Metalworking oil composition

Publications (2)

Publication Number Publication Date
JP2005314558A true JP2005314558A (en) 2005-11-10
JP4769426B2 JP4769426B2 (en) 2011-09-07

Family

ID=35241665

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2004134470A Expired - Fee Related JP4769426B2 (en) 2004-04-28 2004-04-28 Metalworking oil composition

Country Status (4)

Country Link
JP (1) JP4769426B2 (en)
CN (1) CN1946834B (en)
TW (1) TW200609345A (en)
WO (1) WO2005105962A1 (en)

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007154035A (en) * 2005-12-05 2007-06-21 Sumitomo Light Metal Ind Ltd Lubricating oil for tapping machining, and tapping machining method
JP2007297481A (en) * 2006-04-28 2007-11-15 Sumitomo Light Metal Ind Ltd Lubricating oil for machining copper pipe, and manufacturing method of copper pipe using the same
JP2007302791A (en) * 2006-05-11 2007-11-22 Sumitomo Light Metal Ind Ltd Lubricant for processing copper pipe and method for producing copper pipe therewith
JP2008169279A (en) * 2007-01-10 2008-07-24 Sumitomo Light Metal Ind Ltd Lubricating oil for copper pipe machining use and method for producing copper pipe using the same
JP2008179664A (en) * 2007-01-23 2008-08-07 Sumitomo Light Metal Ind Ltd Lubricating oil for processing copper pipe and manufacturing method of copper pipe using the same
JP2009209325A (en) * 2008-03-06 2009-09-17 Idemitsu Kosan Co Ltd Lubricating oil composition for fine blanking
WO2012086564A1 (en) * 2010-12-20 2012-06-28 日本パーカライジング株式会社 Lubricant for plastic processing of metal material
JP2012255085A (en) * 2011-06-09 2012-12-27 Daido Chem Ind Co Ltd Lubricating mold-release agent for hot stamping
JP2016145293A (en) * 2015-02-06 2016-08-12 出光興産株式会社 Water soluble metal processing oil composition and application method thereof
WO2016174923A1 (en) * 2015-04-27 2016-11-03 日本パーカライジング株式会社 Solid lubricant, lubricating coating agent for metal material, surface-treated metal material, and method for forming lubricating coating for metal material
JP2019157141A (en) * 2019-07-01 2019-09-19 日本パーカライジング株式会社 Solid lubricant, lubrication film agent for metal material, surface-treated metal material, and formation method of lubrication film on metal material

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105176647B (en) * 2015-10-14 2018-01-09 苏州市晶协高新电子材料有限公司 A kind of wire cutting oil and preparation method thereof
CN105567392B (en) * 2015-12-23 2018-03-02 南京科润新材料技术有限公司 A kind of drawing lubrication oil
KR102062341B1 (en) * 2017-06-01 2020-01-03 영창케미칼 주식회사 Cutting oil composition and cutting method using the same
CN108865386A (en) * 2018-05-28 2018-11-23 界首市金龙机械设备有限公司 A kind of preparation method of the high-quality cutting fluid of grain machinery work pieces process

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11106778A (en) * 1997-10-08 1999-04-20 Yushiro Chem Ind Co Ltd Flame retardant lubricating oil composition and cutting liquid and cutting method using the same
JP2002294272A (en) * 2001-03-29 2002-10-09 Kyodo Yushi Co Ltd Water dispersible lubricating agent for warm or hot forging and method for forging to process
JP2004115684A (en) * 2002-09-27 2004-04-15 Pentel Corp Water-based ink for ball-point pen
JP2004256630A (en) * 2003-02-25 2004-09-16 Jfe Steel Kk Lubricant composition for rolling and hot-rolling method

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5693596A (en) * 1994-10-25 1997-12-02 Shin-Etsu Handotai Co., Ltd. Cutting fluid, method for production thereof, and method for cutting ingot

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11106778A (en) * 1997-10-08 1999-04-20 Yushiro Chem Ind Co Ltd Flame retardant lubricating oil composition and cutting liquid and cutting method using the same
JP2002294272A (en) * 2001-03-29 2002-10-09 Kyodo Yushi Co Ltd Water dispersible lubricating agent for warm or hot forging and method for forging to process
JP2004115684A (en) * 2002-09-27 2004-04-15 Pentel Corp Water-based ink for ball-point pen
JP2004256630A (en) * 2003-02-25 2004-09-16 Jfe Steel Kk Lubricant composition for rolling and hot-rolling method

Cited By (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007154035A (en) * 2005-12-05 2007-06-21 Sumitomo Light Metal Ind Ltd Lubricating oil for tapping machining, and tapping machining method
JP2007297481A (en) * 2006-04-28 2007-11-15 Sumitomo Light Metal Ind Ltd Lubricating oil for machining copper pipe, and manufacturing method of copper pipe using the same
JP2007302791A (en) * 2006-05-11 2007-11-22 Sumitomo Light Metal Ind Ltd Lubricant for processing copper pipe and method for producing copper pipe therewith
JP2008169279A (en) * 2007-01-10 2008-07-24 Sumitomo Light Metal Ind Ltd Lubricating oil for copper pipe machining use and method for producing copper pipe using the same
JP2008179664A (en) * 2007-01-23 2008-08-07 Sumitomo Light Metal Ind Ltd Lubricating oil for processing copper pipe and manufacturing method of copper pipe using the same
JP2009209325A (en) * 2008-03-06 2009-09-17 Idemitsu Kosan Co Ltd Lubricating oil composition for fine blanking
KR101497252B1 (en) * 2010-12-20 2015-02-27 니혼 파커라이징 가부시키가이샤 Lubricant for plastic processing of metal material
WO2012086564A1 (en) * 2010-12-20 2012-06-28 日本パーカライジング株式会社 Lubricant for plastic processing of metal material
JP5718944B2 (en) * 2010-12-20 2015-05-13 日本パーカライジング株式会社 Lubricant for plastic working of metal materials
JP2012255085A (en) * 2011-06-09 2012-12-27 Daido Chem Ind Co Ltd Lubricating mold-release agent for hot stamping
JP2016145293A (en) * 2015-02-06 2016-08-12 出光興産株式会社 Water soluble metal processing oil composition and application method thereof
WO2016174923A1 (en) * 2015-04-27 2016-11-03 日本パーカライジング株式会社 Solid lubricant, lubricating coating agent for metal material, surface-treated metal material, and method for forming lubricating coating for metal material
JP2016204577A (en) * 2015-04-27 2016-12-08 日本パーカライジング株式会社 Solid lubricant, lubrication film agent for metal material, surface-treated metal material, and formation method of lubrication film on metal material
CN107969134A (en) * 2015-04-27 2018-04-27 日本帕卡濑精株式会社 Kollag, the metal material lubrication envelope forming method for lubricating fruit glaze agent, surface-treated metal material and metal material
CN107969134B (en) * 2015-04-27 2021-07-23 日本帕卡濑精株式会社 Solid lubricant, lubricant coating agent for metal material, surface-treated metal material, and method for forming lubricant coating film of metal material
JP2019157141A (en) * 2019-07-01 2019-09-19 日本パーカライジング株式会社 Solid lubricant, lubrication film agent for metal material, surface-treated metal material, and formation method of lubrication film on metal material

Also Published As

Publication number Publication date
WO2005105962A1 (en) 2005-11-10
JP4769426B2 (en) 2011-09-07
TW200609345A (en) 2006-03-16
CN1946834B (en) 2011-09-14
CN1946834A (en) 2007-04-11

Similar Documents

Publication Publication Date Title
WO2005105962A1 (en) Metalworking fluid composition
TWI415932B (en) Lubricants for metalworking
CN109072116B (en) Metalworking oil composition
JP5134184B2 (en) Low copper corrosive gear oil
CN101280240B (en) Gear oil composition
JP2000144164A (en) Lubricating grease composition
JP5544068B2 (en) Lubricating oil composition for fine blanking
JP2016156028A (en) Fluid compositions with improved wear performance
JP7342085B2 (en) Water-insoluble metalworking oil composition
WO2016158534A1 (en) Cutting and grinding oil composition
CN113302267B (en) Sulfur-based extreme pressure agent and metalworking oil
JP2008274190A (en) Gear oil composition
JP4485390B2 (en) Lubricating oil for processing metal materials
JP3981159B2 (en) Metalworking oil composition
JP3326337B2 (en) Lubricating oil composition for sliding surfaces
JP3501238B2 (en) Metalworking oil composition
CN1161370A (en) metalworking oil composition
JP2008055426A (en) Method of press work for metallic material
JP2007332307A (en) Lubricant for metallic material processing and method for processing metallic material using the same
JP4012292B2 (en) Metalworking oil composition
JP2003213284A (en) Lubricant composition for metal working use
CA2343641A1 (en) A gear oil for improved load-carrying performance at high temperature
JP2014101524A (en) Lubricant composition for fine blanking processing and fine blanking processing method
JP2002155293A (en) Metalworking oil composition
WO2022123857A1 (en) Grease composition, and method for lubricating sliding part using said grease composition

Legal Events

Date Code Title Description
A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20061108

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20100914

A521 Written amendment

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20101111

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20101221

A521 Written amendment

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20110208

A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 20110607

A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20110620

R150 Certificate of patent or registration of utility model

Free format text: JAPANESE INTERMEDIATE CODE: R150

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

Free format text: PAYMENT UNTIL: 20140624

Year of fee payment: 3

LAPS Cancellation because of no payment of annual fees