JPS638489A - Lubricant for metal cold working - Google Patents

Lubricant for metal cold working

Info

Publication number
JPS638489A
JPS638489A JP61151178A JP15117886A JPS638489A JP S638489 A JPS638489 A JP S638489A JP 61151178 A JP61151178 A JP 61151178A JP 15117886 A JP15117886 A JP 15117886A JP S638489 A JPS638489 A JP S638489A
Authority
JP
Japan
Prior art keywords
weight
film
cold working
lubricant
acid
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
JP61151178A
Other languages
Japanese (ja)
Other versions
JPH0437878B2 (en
Inventor
Yoshio Nagaei
永栄 義男
Takashi Kawakami
隆 川上
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.)
Nihon Parkerizing Co Ltd
Original Assignee
Nihon Parkerizing 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 Nihon Parkerizing Co Ltd filed Critical Nihon Parkerizing Co Ltd
Priority to JP61151178A priority Critical patent/JPS638489A/en
Priority to DE8787109098T priority patent/DE3778764D1/en
Priority to DE19873720841 priority patent/DE3720841A1/en
Priority to AT87109098T priority patent/ATE75770T1/en
Priority to EP87109098A priority patent/EP0251192B1/en
Publication of JPS638489A publication Critical patent/JPS638489A/en
Publication of JPH0437878B2 publication Critical patent/JPH0437878B2/ja
Granted legal-status Critical Current

Links

Classifications

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    • 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
    • C10M173/00Lubricating compositions containing more than 10% water
    • C10M173/02Lubricating compositions containing more than 10% water not containing mineral or fatty oils
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    • C10M143/00Lubricating compositions characterised by the additive being a macromolecular hydrocarbon or such hydrocarbon modified by oxidation
    • C10M143/02Polyethene
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    • C10M143/00Lubricating compositions characterised by the additive being a macromolecular hydrocarbon or such hydrocarbon modified by oxidation
    • C10M143/10Lubricating compositions characterised by the additive being a macromolecular hydrocarbon or such hydrocarbon modified by oxidation containing aromatic monomer, e.g. styrene
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    • C10M145/00Lubricating compositions characterised by the additive being a macromolecular compound containing oxygen
    • C10M145/02Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M145/10Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate
    • C10M145/12Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate monocarboxylic
    • C10M145/14Acrylate; Methacrylate
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    • C10M145/00Lubricating compositions characterised by the additive being a macromolecular compound containing oxygen
    • C10M145/02Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M145/10Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate
    • C10M145/16Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate polycarboxylic
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    • C10M149/00Lubricating compositions characterised by the additive being a macromolecular compound containing nitrogen
    • C10M149/02Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M149/06Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to an amido or imido group
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    • C10M149/02Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M149/08Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a nitrile group
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    • C10M159/00Lubricating compositions characterised by the additive being of unknown or incompletely defined constitution
    • C10M159/02Natural products
    • C10M159/06Waxes, e.g. ozocerite, ceresine, petrolatum, slack-wax
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    • C10M2201/02Water
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    • C10M2201/041Carbon; Graphite; Carbon black
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    • C10M2201/04Elements
    • C10M2201/041Carbon; Graphite; Carbon black
    • C10M2201/042Carbon; Graphite; Carbon black halogenated, i.e. graphite fluoride
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    • C10M2201/061Carbides; Hydrides; Nitrides
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    • C10M2201/062Oxides; Hydroxides; Carbonates or bicarbonates
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    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/06Metal compounds
    • C10M2201/065Sulfides; Selenides; Tellurides
    • C10M2201/066Molybdenum sulfide
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    • C10M2201/10Compounds containing silicon
    • C10M2201/105Silica
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    • C10M2201/16Carbon dioxide
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    • C10M2201/18Ammonia
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    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/02Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
    • C10M2205/022Ethene
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    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
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    • C10M2209/103Polyethers, i.e. containing di- or higher polyoxyalkylene groups
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    • C10M2219/04Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
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    • C10N2050/00Form in which the lubricant is applied to the material being lubricated
    • C10N2050/015Dispersions of solid lubricants
    • C10N2050/02Dispersions of solid lubricants dissolved or suspended in a carrier which subsequently evaporates to leave a lubricant coating

Abstract

PURPOSE:An aqueous lubricant for cold working showing improved lubricating properties in use for metal press processing, rolling, wire drawing, drawing of steel tubing, etc., containing a specific thermosetting acrylic resin, wax, a surface active agent and water in a specific ratio. CONSTITUTION:An aqueous lubricant for cold working containing (A)10-35wt% thermosetting acrylic resin having -10-25 deg.C glass transition point, (B) 3-15pts. wt. wax, (C) 0.5-5.0pts.wt. surface active agent and (D) the rest of water in a weight ratio of the component A/B of 2-12. EFFECT:A coating film remaining on the metallic surface after cold working is readily removable with an alkali cleaner.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は、金属のプレス加工、圧延、伸線、鋼管の引扱
き等の冷間加工に於ける金属の冷開加工用1121滑剤
に関するものである。
Detailed Description of the Invention (Field of Industrial Application) The present invention relates to a 1121 lubricant for cold opening of metals in cold workings such as metal pressing, rolling, wire drawing, and handling of steel pipes. It is.

〔従来技術〕[Prior art]

従来、金属を冷間加工する場合、金属及び金型工具の摩
擦や摩耗の低減を図るため、金属にT!I滑剤を施して
おり、そのi11滑剤として、比較的低加工度のものに
対しては、極圧剤や油性向上剤を添加した潤滑油が施さ
れ、高加工度の場合、有機溶剤で希釈して用いる樹脂系
n滑剤が塗布され、更にその上に潤滑油が塗布されてい
る。
Conventionally, when cold working metal, T! As the lubricant, lubricating oil with an extreme pressure agent or oiliness improver added is applied to those with a relatively low working degree, and diluted with an organic solvent in the case of a high working degree. A resin-based lubricant used as a lubricant is applied, and lubricating oil is further applied thereon.

〔発明が解決しようとする問題点〕[Problem that the invention seeks to solve]

近年潤滑剤の用途が多様化しており、冷間加工の条件が
きびしい場合には、これらの潤滑剤では満足できない場
合があることが問題として生じてきた。又有機溶剤で希
釈して用いる樹脂系潤滑剤は環境衛生上よくなく、又、
火災などの危険性もある。又冷間加工後にその残留皮膜
をアルカリクリーナーで容易に除去することができない
ので加工現場に適さないなどの問題も生じてきた。
In recent years, the uses of lubricants have diversified, and the problem has arisen that these lubricants may not be sufficient when cold working conditions are severe. Furthermore, resin-based lubricants that are diluted with organic solvents are not good for environmental hygiene, and
There are also risks such as fire. Further, the residual film cannot be easily removed with an alkaline cleaner after cold working, which has caused problems such as unsuitability for working sites.

そこで強度の冷間加工に対して優れた潤滑性能を示すと
共に冷間加工後に金属表面に残留する皮膜をアルカリク
リーナーで容易に除去できるような金属のrIi消剤が
必要となってきた。
Therefore, there has been a need for an rIi eraser for metals that exhibits excellent lubrication performance for intense cold working and that allows the film remaining on the metal surface to be easily removed with an alkaline cleaner after cold working.

〔問題点を解決するための手段〕[Means for solving problems]

前記要望に応じた潤滑剤を開発すべく鋭意研究した結果
、ガラス転移点が一10〜25℃に調整された熱硬化型
アクリル系樹脂10〜15℃旦部とワックス3〜15東
学部と界面活性剤05〜5重聞部と残りは水を含有し、
且つ前記熱硬化型アクリル系樹脂/ワックス重量比が2
〜12に調整された水性液で処理し、常温乾燥後、加熱
、焼付けすると、従来のTII滑剤を用いるよりも優れ
た潤滑皮膜を得ることが出来た。
As a result of intensive research to develop a lubricant that meets the above-mentioned needs, we found that a thermosetting acrylic resin with a glass transition point adjusted to 110 to 25 degrees Celsius (10 to 15 degrees Celsius), a wax 3 to 15 degrees Celsius, and an interface between The activator 05 to 5 parts and the rest contain water,
and the thermosetting acrylic resin/wax weight ratio is 2
When treated with an aqueous liquid adjusted to 12 to 12, dried at room temperature, heated and baked, it was possible to obtain a lubricating film superior to that obtained using conventional TII lubricants.

本発明におけるガラス転移点−10〜15℃の熱硬化型
アクリル系樹脂は、一般式 %式% 〔式中のRa 、Rb 、Rc 、Rdの順位はランダ
ムであり、Raはビニルトルエン基、スチレン基、メチ
ルメタアクリル基又はアクリルニトリル基の中から選ば
れた1種又は2種以上を20〜70重M%からなり、R
bはアクリル酸と炭素数1〜12を有する1級脂肪族ア
ルコールとの反応により得られたアクリル酸エステル及
び/又はメタクリル酸と炭素数3〜12を有する1級脂
肪族アルコールとの反応により得られたメタクリル醒エ
ステルを20〜70i1fi%からなり、RCはアクリ
ル酸、メタクリル酸、マレイン酸、イタコン酸、2〜ヒ
ドロキシエチルメタクリレートのリン酸エステル化合物
、2−ヒトOキシプロピルメタクリレートのリン酸エス
テル化合物、又はそれらのアルカリ中和物の中から選ば
れた1種又は2種以上を1〜15重固%からなり、l”
(dはメタクリル酸2−ヒドロ4:シルエチル、メタク
リル酸ヒドロキシプロピル、アクリル酸2−ヒドロキシ
ルエチル、アクリル酸ヒドロキシプロピル、N−メヂロ
ールアクリルアミド又はそのエステル化合物、ジアセト
ンアクリルアミド又はグリシジルメタクリレートの中か
ら選ばれた1種又は2種以上を1〜20重伍%からなっ
ている。〕を有する熱硬化型アクリル系樹脂を用いるこ
とが出来る。nは重合度1000〜so、 oooであ
るが、ガラス転移点−10〜25℃になるように重合さ
せる。例えば、各七ツマ−の混合物を50〜60℃で5
〜7時間乳化重合させることにより所望のガラス転移点
を得ることが出来る。他の重合方法としては、例えば、
溶液重合、!ll濁重合などがある。
The thermosetting acrylic resin with a glass transition point of -10 to 15°C in the present invention has the general formula % [In the formula, the order of Ra, Rb, Rc, and Rd is random, and Ra is a vinyltoluene group, R
b is an acrylic ester obtained by the reaction of acrylic acid with a primary aliphatic alcohol having 1 to 12 carbon atoms, and/or an acrylic ester obtained by the reaction of methacrylic acid with a primary aliphatic alcohol having 3 to 12 carbon atoms; RC is a phosphoric acid ester compound of acrylic acid, methacrylic acid, maleic acid, itaconic acid, 2-hydroxyethyl methacrylate, and a phosphoric acid ester compound of 2-human O-oxypropyl methacrylate. , or one or more selected from alkali neutralized products thereof, in an amount of 1 to 15% by weight, l''
(d is selected from methacrylic acid 2-hydro 4: sylethyl, hydroxypropyl methacrylate, 2-hydroxylethyl acrylate, hydroxypropyl acrylate, N-medyrollacrylamide or its ester compound, diacetone acrylamide or glycidyl methacrylate) It is possible to use a thermosetting acrylic resin having 1 to 20 wt. Polymerize at -10 to 25°C. For example, a mixture of each seven polymer is polymerized at 50 to 60°C for 50 to 60°C.
A desired glass transition point can be obtained by carrying out emulsion polymerization for ~7 hours. Other polymerization methods include, for example,
Solution polymerization! Examples include turbid polymerization.

重合方法により水以外の溶媒を使用する場合があり、例
えば、エタノール、イソプロピルアルコール等を使用す
る場合がある。
Depending on the polymerization method, a solvent other than water may be used; for example, ethanol, isopropyl alcohol, etc. may be used.

本発明に用いられるワックスは、石油パラフィンワック
ス、動植物油脂、高級脂肪酸、高級アルコール、高級脂
肪酸と高級アルコールエステル、高級脂肪酸アマイド、
高級脂肪酸のアミン塩などが挙げられ、TII滑剤皮膜
を固化させておくために融点が45℃以上のものを用い
るのが好ましい。融点を上げるには、水素添加により2
重結合をなくす方法がある。
The waxes used in the present invention include petroleum paraffin wax, animal and vegetable oils, higher fatty acids, higher alcohols, higher fatty acids and higher alcohol esters, higher fatty acid amides,
Examples include amine salts of higher fatty acids, and it is preferable to use those with a melting point of 45° C. or higher in order to solidify the TII lubricant film. To raise the melting point, hydrogenation increases the
There is a way to eliminate double bonds.

界面活性剤は、ワックスを水に乳化分散させるために用
いられるが、その界面活性剤としては、アニオン系界面
活性剤、ノニオン系界面活性剤が挙げられる。アニオン
系界面活性剤は、アルキルナフタレンスルフオン酸ナト
リウム、アルキルベンゼンスルフオン酸ナトリウム、ロ
ート油などが挙げられ、ノニオン系界面活性剤としては
、ポリオキシエチレンアルキルエーテル(アルキル基は
高級アルコール)系、ポリオキシエチレンノニルフェノ
ールエーテル系、脂肪酸とポリエチレングリコールエス
テル、脂肪酸とソルビタンエステル、及びエチレンオキ
サイド付加物、などが挙げられる。界面活性剤によりあ
る程度の乳化分散が出来るがさらに乳化性の向上を図る
ため、ホモジナイザーなどの機械撹拌と併用してもよい
Surfactants are used to emulsify and disperse wax in water, and examples of the surfactants include anionic surfactants and nonionic surfactants. Examples of anionic surfactants include sodium alkylnaphthalene sulfonate, sodium alkylbenzenesulfonate, and funnel oil. Examples of nonionic surfactants include polyoxyethylene alkyl ether (the alkyl group is a higher alcohol) type, polyester, etc. Examples include oxyethylene nonylphenol ethers, fatty acids and polyethylene glycol esters, fatty acids and sorbitan esters, and ethylene oxide adducts. Although a certain degree of emulsification and dispersion can be achieved using a surfactant, mechanical stirring such as a homogenizer may be used in combination to further improve the emulsifying property.

本発明の潤滑剤に、固体11滑剤を配合してもよい。固
体潤滑剤は、例えば、グラファイト、2硫化モリブデン
、タルク、テフロン、窒化ホウ素、炭酸カルシウム、メ
ラミン・イソシアヌル酸付加物などが挙げられる。
A solid 11 lubricant may be incorporated into the lubricant of the present invention. Examples of the solid lubricant include graphite, molybdenum disulfide, talc, Teflon, boron nitride, calcium carbonate, and melamine-isocyanuric acid adduct.

[作 用] 熱硬化型アクリル系樹脂を用いた理由は、金属の冷間加
工により、金属や工具が発熱する。この発熱は、強加工
度や連続的な加工により更に蓄熱してくる。ここで潤滑
剤の成分に熱可塑型アクリル系樹脂を使用した場合常温
では固体皮膜であるが、加工により金属や工具が上界す
ると、ガラス転移点以上となった場合、流動性が出てく
る。
[Function] The reason for using a thermosetting acrylic resin is that the metal and tools generate heat during cold working of the metal. This heat generation further accumulates due to heavy working and continuous working. When a thermoplastic acrylic resin is used as a lubricant component, it forms a solid film at room temperature, but when the metal or tool is processed and the temperature exceeds the glass transition point, it becomes fluid. .

この状態では、金属と工具との直接接触の防止する能力
が低くなり、加工条件が厳しくなった場合しごき取られ
て焼付きが発生する。
In this state, the ability to prevent direct contact between the metal and the tool is reduced, and if the processing conditions become severe, the tool will be squeezed out and seizure will occur.

従って、高温時にお(プる固体皮膜とすることが、重要
であり、このため熱硬化型アクリル系樹脂を利用するこ
とにより解決した。
Therefore, it is important to form a solid film that evaporates at high temperatures, and this problem was solved by using a thermosetting acrylic resin.

しかし通常の熱硬化型樹脂の欠点としては樹脂が硬化し
た場合樹脂皮膜が硬くなるが塑性変形により、金属の延
びに対して、樹脂皮膜が追ずいしずらくなるため皮膜切
れが起って金属と工具の直接接触して、焼付きが発生し
やすくなる。又、冷間加工後にrR滑皮膜を除去するこ
とが必要であるが、熱硬化した皮膜は、アルカリによる
除去は・難しい・この改善として、樹脂の電橋は可撓性
のよい構造の自己架橋タイプがよく、又、その架橋割合
いも少なくする。しかし樹脂自体の特性値としては、軟
い方がよく伸びるため、金属の伸びに皮膜が追ずいしや
すくなる。従って、ガラス転移点が一10〜25℃と低
い方が軟くて伸びがよい。−10℃未満では、皮膜が軟
らかくなりすぎて冷間加工時に焼付きが発生しやすくな
る。25℃以上では、皮膜が硬くなりすぎ金属加工時の
金属の伸びに対する皮膜の追ずい性が低下したり又冬期
の寒い時期には、造膜性が悪くなる傾向があり均一な皮
膜の生成が難しい。好ましいのは0〜5℃である。
However, the disadvantage of normal thermosetting resins is that when the resin hardens, the resin film becomes hard, but due to plastic deformation, it becomes difficult for the resin film to follow the elongation of the metal. If the tool comes into direct contact with the tool, seizure is likely to occur. In addition, it is necessary to remove the rR slipping film after cold working, but it is difficult to remove the heat-cured film with alkali.To improve this, the resin electrical bridge has a self-crosslinking structure with good flexibility. The type is good, and the crosslinking rate is also reduced. However, in terms of the characteristic values of the resin itself, the softer it is, the better it stretches, so the film can more easily follow the expansion of the metal. Therefore, the lower the glass transition point is from 110 to 25°C, the softer and better the elongation. If the temperature is less than -10°C, the film becomes too soft and seizure is likely to occur during cold working. At temperatures above 25°C, the film becomes too hard and its ability to follow the elongation of the metal during metal processing decreases, and in the cold winter months, film forming properties tend to deteriorate, making it difficult to form a uniform film. difficult. Preferably it is 0-5°C.

前記熱硬化型アクリル系樹脂の一般式中のRaは、皮膜
の硬度及び引張り強度を持たぼるもので20〜70! 
1%含有させるのが好ましい。Rbは、皮膜に軟かさと
延伸性を持たUるものを20〜70重a%含有させるの
が好ましい。RCは、金属との密着性、乳化分散性を向
上させるもので、1〜15重信%含有させるのが好まし
い。Rdは、金属との密着性を向上させ、又加熱すると
RCのカルボキシル基と架橋し硬化して、耐熱性を向上
さゼるのに必要であり1〜20m m%金含有せるのが
好ましい。
Ra in the general formula of the thermosetting acrylic resin increases the hardness and tensile strength of the film, and is 20 to 70!
It is preferable to contain 1%. It is preferable that Rb contains 20 to 70% by weight of Rb, which gives the film softness and stretchability. RC improves adhesion with metals and emulsification dispersibility, and is preferably contained in an amount of 1 to 15%. Rd is necessary to improve adhesion to metals and to crosslink with the carboxyl group of RC and harden when heated to improve heat resistance, and preferably contains 1 to 20 mm% of gold.

Ra 20%未満では、樹脂皮膜の硬度がやわらかくて塑性加
工時に皮膜がしごき取られて焼付きが発生してよくない
。70%を越えるとガラス転位点(TG)が高くなりす
ぎて室温における皮膜の造膜性が悪くなり塑性加工時に
焼付きが発生してよくない。
If Ra is less than 20%, the hardness of the resin film is soft and the film is rubbed off during plastic working, causing seizure, which is not good. If it exceeds 70%, the glass transition point (TG) becomes too high, which deteriorates the film forming properties of the film at room temperature and causes seizure during plastic working, which is not good.

Rb 20%未満では、TG//高くなりずぎて、室温におけ
る皮膜の造膜性が恕くなり塑性加工時に焼付きが発生し
てよくない、、70%を越えると皮膜の硬度が軟らかく
て塑性加工時に皮膜がしこぎ取られて焼付きが発生する
If Rb is less than 20%, TG// becomes too high and the film forming properties of the film at room temperature are poor, causing seizure during plastic working, which is not good. If it exceeds 70%, the hardness of the film becomes soft. During plastic working, the film is scraped off and seizure occurs.

すなわち、RaとRbは相反する特性を持っており、R
aとRbをうまく組合せることにより焼付ぎの発生が防
止できる。
In other words, Ra and Rb have contradictory characteristics, and R
Occurrence of seizure can be prevented by properly combining a and Rb.

Rc 1%未満では、 ■ 金属に対する密着性が低下する。Rc Less than 1%, ■ Adhesion to metal decreases.

■ 皮膜をアルカリ脱脂液で除去する場合に除去できな
い。
■ The film cannot be removed using alkaline degreasing solution.

■ Rdのヒドロキシアル4ニルメタクリレート、N−
メチロールアクリルアミド又はグリシジルメタクリレー
トとの架橋反応が促進されず耐熱性が低下する。
■ Rd hydroxyal4nyl methacrylate, N-
The crosslinking reaction with methylol acrylamide or glycidyl methacrylate is not promoted, resulting in a decrease in heat resistance.

15%を越えると、 ■ 処理液の粘度が高くなりすぎて作業性や塗布性がう
まく行かない。
If it exceeds 15%, (1) the viscosity of the treatment liquid becomes too high, resulting in poor workability and coating properties.

■ 生成した皮膜(よ、吸θ性が高くなり、造膜後長期
間放置した場合吸湿により皮膜の密着性が低下する。
■ The resulting film has high θ absorption properties, and if left for a long period of time after film formation, the adhesion of the film will decrease due to moisture absorption.

Rd 1%未1号では、 ■ 架橋が不充分で耐熱性がよくない。Rd In 1% non-No. 1, ■ Heat resistance is poor due to insufficient crosslinking.

20%を越えると、 ■ 架橋が進みすぎた皮膜となるため、可撓性がなくな
り、塑性加工時に皮膜が金属の延びに追ずいしなくなり
焼付きが発生してよくない。ヒドロキシアルキルメタク
リレートは、5〜15%が好ましく、N−メチロールア
クリルアミド又はグリシジルメタクリレートは1〜5%
が好ましい。
If it exceeds 20%, (1) the film becomes too cross-linked and loses its flexibility, and the film cannot follow the elongation of the metal during plastic working, causing seizure, which is not good. Hydroxyalkyl methacrylate is preferably 5 to 15%, and N-methylolacrylamide or glycidyl methacrylate is 1 to 5%.
is preferred.

熱硬化型アクリル系樹脂とワックスとの混合比は虫型な
因子であり、前記熱硬化型アクリル系樹脂にワックスを
適量混合させることにJ:って金属表面上の樹脂皮膜の
除去性及び潤滑性を向上させる。熱硬化型アクリル系樹
脂/ワックスI門比が2未満になると、金属に形成され
る皮膜の密着性が低下して金属を塑性変形加工している
時に膜切れを起して焼付く。又12を超えると滑り性が
低下して金属間の1!E擦が大きくなり焼付く。好まし
くは、4〜6の範囲である。潤滑剤処理液中の界面活性
剤の適正添加濃度は、余り多聞に添加すると潤滑性を低
下させるので1.71化分散させるのに必要な添加濃度
及び1司滑性を考1!ヨすると0.5〜5重番部が良い
。界面活性剤としては、ノニオン系、アニオン系、カチ
オン系、両性イオン系が挙げられる。好ましいのはノニ
オン系、アニオン系である。
The mixing ratio of the thermosetting acrylic resin and wax is a major factor, and mixing an appropriate amount of wax with the thermosetting acrylic resin improves the removability and lubrication of the resin film on the metal surface. Improve your sexuality. When the thermosetting acrylic resin/wax I ratio is less than 2, the adhesion of the film formed on the metal decreases, causing the film to break and seize during plastic deformation of the metal. Moreover, when it exceeds 12, the slipperiness decreases and the 1! E The friction becomes large and seizes up. Preferably, it is in the range of 4-6. The appropriate addition concentration of the surfactant in the lubricant treatment liquid is 1.71, as adding too much will reduce the lubricity, so consider the addition concentration necessary for dispersion and the 1.71 lubricity. If so, 0.5 to 5 parts are good. Examples of the surfactant include nonionic, anionic, cationic, and amphoteric surfactants. Preferred are nonionic and anionic types.

本発明の潤滑剤処理液を金属に適用するには、予め脱脂
した金属を浸漬法、スプレー法、ハケ塗り法、流しかけ
法、〔l−ルコーター法等の方法により常温にて処理し
、乾燥するが、乾燥にあたり予め自然乾燥してから80
〜120℃にて加熱焼付けする方が密着性が向上するの
で好ましい。形成させる皮膜は、塑性変形方法に応じて
皮膜伍を変化させ、板のような軽度の加工度の場合0.
5〜59/Trt1バイブのような強1)[1工度の場
合5〜30g/尻になるように処理液濃度を変化さけて
処理形成さける。
To apply the lubricant treatment liquid of the present invention to metal, pre-degreased metal is treated at room temperature by a method such as dipping, spraying, brushing, pouring, or l-coater, and then dried. However, when drying, please dry it naturally beforehand.
It is preferable to heat and bake at a temperature of 120° C. to 120° C. since this improves adhesion. The thickness of the film to be formed changes depending on the plastic deformation method.
5-59/Trt1 vibrator-like strength 1) [In the case of 1 process, avoid changing the concentration of the processing solution so that it becomes 5-30 g/bottom to avoid processing formation.

実施例 1 SO3304のステンレスf14管を酸洗し、水洗し、
第1表及び第2表の熱硬化型アクリル系樹脂とワックス
を含有する処理液で浸油処理(20℃、1分)し、1時
間液切りと自然乾燥した後、100℃の熱風で30分間
乾燥して固体皮膜を10〜15U/尻形成させた。伸管
礪で引抜き加工を行い、引抜き後の外観観察及び潤滑膜
の除去法について調査した。
Example 1 SO3304 stainless steel F14 pipe was pickled, washed with water,
Oil immersion treatment (20°C, 1 minute) with a treatment solution containing thermosetting acrylic resin and wax shown in Tables 1 and 2, followed by draining for 1 hour and air drying, followed by 30°C with hot air at 100°C. Dry for minutes to form a solid film of 10-15 U/bottle. Drawing was performed using a stretched tube, and the appearance after drawing was observed and the method for removing the lubricant film was investigated.

その結果を第3表に示す。The results are shown in Table 3.

伸管条件 ・ステンレス鋼管 25φX 2.5t X 200O
N  (rtm )・ 加  工  度     32
′%・引抜き速度   17.8m / min又Sυ
S 30450X 100 X  0.8mtn材料を
、同様の処理液及び条件で試験板を作成しバウデン試験
ぼにより、摩擦係数及び焼付きまでの摺動回数を測定し
た。表4に承り。
Tube stretching conditions: Stainless steel pipe 25φX 2.5t X 200O
N (rtm)・Processing degree 32
'%・Drawing speed 17.8m/min or Sυ
A test plate was prepared using the S 30450 x 100 x 0.8 mtn material using the same treatment solution and conditions, and the friction coefficient and number of sliding movements until seizure were measured using the Bowden test. Table 4 is accepted.

(バウデン試験、条件〕 1F 子;5UJ−25φ 1、η  単:5にり 摺動速度: IOM/SeC 店動幅;30mm 試験5 ; SO330450X 100 X O,8
〃+m試験渇瓜:25℃ 比較例 1 実施例と同様のステンレス鋼管を酸洗、水洗し、蓚M塩
皮膜化成処理(FB−A(日本バーカライジング株式会
礼製品) 35g/N 、 AC16,1g/fJ 。
(Bauden test, conditions) 1F: 5UJ-25φ 1, η Single: 5 sliding speed: IOM/SeC Shop movement width: 30mm Test 5; SO330450X 100X O, 8
〃+m test dehydration: 25°C Comparative Example 1 The same stainless steel pipe as in the example was pickled, washed with water, and treated with a salt film chemical conversion treatment (FB-A (Nippon Vercalizing Co., Ltd. product) 35g/N, AC16, 1g/fJ.

90℃、 10分処理]して水洗し、次いで潤滑処理し
〔ボンダリューベ235(日本バー力ライジング株式会
社製品) 70g/、fl 、 80℃、3分処理〕し
て乾燥後、実施例1と同様の抽伸条件により用法き加■
と、バウデン試験を行った。その結果を第3表、第4表
に示す。
90°C for 10 minutes], washed with water, then lubricated [Bondalube 235 (product of Nippon Bar Rising Co., Ltd.) 70g/fl, 80°C for 3 minutes], dried, and then prepared as in Example 1. Additional usage using similar drawing conditions
I conducted the Bauden test. The results are shown in Tables 3 and 4.

比較例 2 実施例1と同様のステンレス鋼管を酸洗、水洗し、乾燥
後溶剤希釈型樹脂(ハングスターフシ111 QD (
ハングスターフア社装品))トルエンで 72倍希釈し
浸油処理(室温1分)し、1日間自然乾燥した後潤滑油
LJ−1(ハングスターフシ・社製品)〕を塗布後、実
施例と同様の抽伸条件にJ、り川辺き加工と、バウデン
試験を11つだ。
Comparative Example 2 The same stainless steel pipe as in Example 1 was pickled, washed with water, dried, and then treated with a solvent-diluted resin (Hangstarfushi 111 QD).
After applying lubricating oil LJ-1 (Hangstarfushi product)], diluted 72 times with toluene, immersed in oil (room temperature for 1 minute), and air-dried for 1 day. 11 J, riverside processing, and Bowden test under the same drawing conditions.

樹脂付着量10び/mとしlど。その結果を第3表、第
4表に承り。
The resin adhesion amount is 10 bi/m. The results are shown in Tables 3 and 4.

比較例 3 実施例1の潤滑剤ff1l!l!液組成No、 1で樹
脂Na 1の架橋成分Rdを除いた以外は実施例1で行
った方法と同様の条件で処理し、引仇き加工とバウデン
試験を行った。樹脂皮膜厚さ10〜15g/尻とした。
Comparative Example 3 Lubricant of Example 1 ff1l! l! Processing was performed under the same conditions as in Example 1 except that the crosslinking component Rd of resin Na 1 was removed using liquid composition No. 1, and subsequent processing and Bowden test were performed. The resin film thickness was 10 to 15 g/bottom.

比較例 4 実施例1のill滑剤処理液組成No3で樹脂Nα2の
架橋成分Rdを除いた以外は、実施例1で行っlζ方法
と同様の条件で処理し引扱き加工とバウデン試験を行っ
た。樹脂圧110Jつざ1o〜+5LJ/尻とした。
Comparative Example 4 A treatment was carried out under the same conditions as in the lζ method in Example 1, except that the crosslinking component Rd of the resin Nα2 was removed from the ill lubricant treatment liquid composition No. 3 in Example 1, and handling processing and Bauden test were performed. The resin pressure was 110J to +5LJ/bottom.

その結果を第3表、第4表示す。The results are shown in Tables 3 and 4.

第 3 表  試 験 結 果  加工度33%ステン
レスバイブの抽伸性能 バウデン試験  表−4 ※1は、値の小さいほど滑り性がよい。
Table 3 Test results Bowden test on drawing performance of stainless steel vibrator with working degree of 33% Table 4 *1: The smaller the value, the better the slipperiness.

※2は、摺動回数の多い程耐焼付き性能がよい。*2: The higher the number of sliding movements, the better the anti-seizure performance.

抽伸後の潤滑膜の除去試験 抽伸後のステンレスm管を苛性ソーダ3%、トリポリリ
ン酸ソーダ1.5%及び界面活性剤を含有する90℃の
アルカリ脱脂剤水溶液に1時間浸漬処理した後潤滑膜の
除去性を目視判定した。
Removal test of lubricating film after drawing After drawing, the stainless steel m-tube was immersed for 1 hour in an alkaline degreasing aqueous solution at 90°C containing 3% caustic soda, 1.5% sodium tripolyphosphate, and a surfactant. The removability was visually judged.

第3表から明らかなように、本願発明の潤滑処理方法に
よりステンレスバイブ表面に形成された潤滑皮膜は引扱
き加工試験において比較例と比較して優れた潤滑効果を
示した。又、引抜き加工後の鋼板表面に残留する潤滑膜
の除去性は実施例においては何れも完全に除去できたの
で優れており、それに対して比較例においては除去性が
極めて悪いのではるかに劣る結果を示した。又、第4表
から明らかなように、ステンレス鋼板表面に形成された
′!II滑皮膜は、バウデン試験において比較例と比較
して優れたS擦係数(低い程滑り性がよい)と耐摩耗焼
付き性を示した。
As is clear from Table 3, the lubricating film formed on the surface of the stainless steel vibrator by the lubrication treatment method of the present invention showed superior lubricating effect in the handling test compared to the comparative example. In addition, the removability of the lubricant film remaining on the surface of the steel plate after drawing was excellent in both examples as it was completely removed, whereas in the comparative example the removability was extremely poor and the result was far inferior. showed that. Also, as is clear from Table 4, '!' formed on the surface of the stainless steel plate. The II synovial film showed superior S friction coefficient (the lower the slipperiness, the better the slipperiness) and abrasion seizure resistance compared to the comparative example in the Bauden test.

(発明の効果〕 本発明の冷間加工用IIjl?11剤処理液にて金属を
処理し、乾燥してその表面に0.5〜309/mの固体
皮膜を形成させると、冷間加工の初期段階で固体皮膜は
充分な潤滑性を示し、しごきに対してもはく離せず従っ
て加工金層表面に皮膜が残留するので金属と金型工具と
の接触が防止できる。変形加工段階では、金属の変形熱
及び摩擦熱により金属表面が100〜150℃上界して
樹脂皮膜の伸びが良くなり、金属の変形に対しよく追随
し膜切れを起さないために、焼付現象が起きない。冷間
加工後においてはその残菌皮膜をアルカリクリーナーで
容易に除去することができるので、加工現場における作
業性に適するものとなる等の優れた効果を奏する。
(Effects of the Invention) When a metal is treated with the cold working IIjl?11 treatment liquid of the present invention and dried to form a solid film of 0.5 to 309/m on the surface, cold working In the initial stage, the solid film exhibits sufficient lubricity and cannot be peeled off even during ironing, so the film remains on the surface of the processed gold layer, preventing contact between the metal and the mold tool.In the deformation process, the metal Due to the heat of deformation and heat of friction, the temperature of the metal surface rises to 100-150°C, which improves the elongation of the resin film, which follows the deformation of the metal well and does not cause film breakage, so no seizure occurs. After the preliminary processing, the residual bacteria film can be easily removed with an alkaline cleaner, resulting in excellent effects such as being suitable for workability at the processing site.

特許出願人 日本パー力ライジング株式会社代  理 
 人   秋   元   11    雄   ・1
1じ、二まで
Patent applicant: Japan Pariki Rising Co., Ltd. Agent
Person Akimoto 11 Male ・1
1st and 2nd

Claims (2)

【特許請求の範囲】[Claims] (1)ガラス転移点が−10〜25℃に調整された熱硬
化型アクリル系樹脂10〜35重量部とワックス3〜1
5重量部と界面活性剤0.5〜5.0重量部と残りは水
を含有し、且つ前記熱硬化型アクリル系樹脂/ワックス
重量比が2〜12に調整された水性液であることを特徴
とする金属の冷間加工用潤滑剤。
(1) 10 to 35 parts by weight of thermosetting acrylic resin whose glass transition point is adjusted to -10 to 25°C and 3 to 1 part of wax
5 parts by weight of surfactant, 0.5 to 5.0 parts by weight of surfactant, and the remainder contains water, and the thermosetting acrylic resin/wax weight ratio is adjusted to 2 to 12. A lubricant for cold working of metals.
(2)前記熱硬化型アクリル系樹脂が一般式−(Ra−
Rb−Rc−Rd)−_n 〔式中のRa、Rb、Rc、Rdの順位はランダムであ
り、nは重合度で1000〜50,000あり、Raは
ビニルトルエン基、スチレン基、メチルメタアクリル基
又はアクリルニトリル基の中から選ばれた1種又は2種
以上を20〜70重量%からなり、Rbはアクリル酸と
炭素数1〜12を有する1級脂肪族アルコールとの反応
により得られたアクリル酸エステル及び/又はメタクリ
ル酸と炭素数3〜12を有する1級脂肪族アルコールと
の反応により得られたメタクリル酸エステルを20〜7
0重量%からなり、Rcはアクリル酸、メタクリル酸、
マレイン酸、イタコン酸、2−ヒドロキシエチルメタク
リレートのリン酸エステル化合物、2−ヒドロキシプロ
ピルメタクリレートのリン酸エステル化合物、又はそれ
らのアルカリ中和物の中から選ばれた1種又は2種以上
を1〜15重量%からなり、Rdはメタクリル酸2−ヒ
ドロキシルエチル、メタクリル酸ヒドロキシプロピル、
アクリル酸2−ヒドロキシルエチル、アクリル酸ヒドロ
キシプロピル、N−メチロールアクリルアミド又はその
エステル化合物、ジアセトンアクリルアミド又はグリシ
ジルメタクリレートの中から選ばれた1種又は2種以上
を1〜20重量%からなっている。〕を有していること
を特徴とする特許請求の範囲第1項記載の金属の冷間加
工用潤滑剤。
(2) The thermosetting acrylic resin has the general formula -(Ra-
Rb-Rc-Rd)-_n [In the formula, the order of Ra, Rb, Rc, and Rd is random, n is the degree of polymerization and is 1000 to 50,000, and Ra is a vinyltoluene group, a styrene group, or a methyl methacrylic group. 20 to 70% by weight of one or more selected from acrylonitrile and acrylonitrile groups, Rb is obtained by reaction of acrylic acid with a primary aliphatic alcohol having 1 to 12 carbon atoms. A methacrylic ester obtained by reacting an acrylic ester and/or methacrylic acid with a primary aliphatic alcohol having 3 to 12 carbon atoms is
0% by weight, Rc is acrylic acid, methacrylic acid,
One or more selected from maleic acid, itaconic acid, phosphoric acid ester compounds of 2-hydroxyethyl methacrylate, phosphoric acid ester compounds of 2-hydroxypropyl methacrylate, or alkali neutralized products thereof. 15% by weight, Rd is 2-hydroxylethyl methacrylate, hydroxypropyl methacrylate,
It consists of 1 to 20% by weight of one or more selected from 2-hydroxylethyl acrylate, hydroxypropyl acrylate, N-methylolacrylamide or its ester compound, diacetone acrylamide, or glycidyl methacrylate. ] The lubricant for cold working of metals according to claim 1, characterized in that it has the following.
JP61151178A 1986-06-27 1986-06-27 Lubricant for metal cold working Granted JPS638489A (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
JP61151178A JPS638489A (en) 1986-06-27 1986-06-27 Lubricant for metal cold working
DE8787109098T DE3778764D1 (en) 1986-06-27 1987-06-24 LUBRICANTS FOR METAL FORMING.
DE19873720841 DE3720841A1 (en) 1986-06-27 1987-06-24 LUBRICANTS FOR METAL FORMING
AT87109098T ATE75770T1 (en) 1986-06-27 1987-06-24 METAL FORMING LUBRICANT.
EP87109098A EP0251192B1 (en) 1986-06-27 1987-06-24 Lubricant for metal formation

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61151178A JPS638489A (en) 1986-06-27 1986-06-27 Lubricant for metal cold working

Publications (2)

Publication Number Publication Date
JPS638489A true JPS638489A (en) 1988-01-14
JPH0437878B2 JPH0437878B2 (en) 1992-06-22

Family

ID=15513003

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61151178A Granted JPS638489A (en) 1986-06-27 1986-06-27 Lubricant for metal cold working

Country Status (4)

Country Link
EP (1) EP0251192B1 (en)
JP (1) JPS638489A (en)
AT (1) ATE75770T1 (en)
DE (2) DE3778764D1 (en)

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US5368757A (en) * 1991-03-22 1994-11-29 Henkel Corporation Lubrication for cold forming of metals
US5547595A (en) * 1995-02-07 1996-08-20 Henkel Corporation Aqueous lubricant and process for cold forming metal, particularly pointing thick-walled metal tubes
CN101993770A (en) * 2010-11-18 2011-03-30 江南大学 Lubricating agent for high-speed wire drawing and preparation method thereof
JP2015183150A (en) * 2014-03-26 2015-10-22 貴和化学薬品株式会社 Lubricant for plastic processing
CN112588846A (en) * 2020-11-23 2021-04-02 江阴法尔胜泓昇不锈钢制品有限公司 Production process of alloy steel wire for cold heading

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3916128A1 (en) * 1989-05-18 1990-11-22 Roehm Gmbh AQUEOUS FUNCTIONAL LIQUIDS CONTAINING THICKENING AGENTS ON A POLY (METH) ACRYLATE BASE
DE4445993A1 (en) * 1994-12-22 1996-06-27 Metallgesellschaft Ag Lubricant for metal forming
US6899770B1 (en) 1999-03-04 2005-05-31 Henkel Corporation Composition and process for treating metal surfaces
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JP4668826B2 (en) * 2006-03-31 2011-04-13 住友金属工業株式会社 Cold drawing method for metal and method for producing drawn material
JP4597896B2 (en) * 2006-03-31 2010-12-15 住友金属工業株式会社 Cold drawing method and method for producing drawn tube
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CN101993770A (en) * 2010-11-18 2011-03-30 江南大学 Lubricating agent for high-speed wire drawing and preparation method thereof
JP2015183150A (en) * 2014-03-26 2015-10-22 貴和化学薬品株式会社 Lubricant for plastic processing
CN112588846A (en) * 2020-11-23 2021-04-02 江阴法尔胜泓昇不锈钢制品有限公司 Production process of alloy steel wire for cold heading

Also Published As

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DE3720841A1 (en) 1988-01-14
ATE75770T1 (en) 1992-05-15
JPH0437878B2 (en) 1992-06-22
EP0251192A2 (en) 1988-01-07
EP0251192A3 (en) 1988-05-04
EP0251192B1 (en) 1992-05-06
DE3778764D1 (en) 1992-06-11

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