JPH04514B2 - - Google Patents
Info
- Publication number
- JPH04514B2 JPH04514B2 JP61011100A JP1110086A JPH04514B2 JP H04514 B2 JPH04514 B2 JP H04514B2 JP 61011100 A JP61011100 A JP 61011100A JP 1110086 A JP1110086 A JP 1110086A JP H04514 B2 JPH04514 B2 JP H04514B2
- Authority
- JP
- Japan
- Prior art keywords
- resin
- lubricating
- solid powder
- water
- weight
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
Landscapes
- Lubricants (AREA)
- Forging (AREA)
Description
[産業上の利用分野]
この発明は、自動車や建設機械、農機具等の各
種の部品、各種工具の部品、電気機器の各種の部
品等を温間鍛造で製造する際にその前処理として
行われる潤滑処理方法に関する。
[従来の技術]
金属材料の鍛造を行う際の鍛造方式には大きく
分けて冷間、温間及び熱間の3方式が知られてお
り、それぞれの長所及び短所については多くの文
献等で報告されているが、精度を要求される加工
では温間域での鍛造が品質的にもエネルギー的に
も最も優れているとされている。
そして、この温間鍛造を行う際には、その前処
理として金属材料の表面の潤滑処理が行われる
が、従来においては固体潤滑剤の水分散液又は油
分散液中に金属材料を浸漬するか、この金属材料
に上記固体潤滑剤の水分散液又は油分散液を噴霧
等で塗布することが行なわれている。
[発明が解決しようとする問題点]
しかしながら、上記従来の潤滑処理方法では、
金属材料の表面に形成される潤滑被膜の強度が不
足したり、温間鍛造時に固体潤滑剤の新生面への
導入等が不足し、加工度が小さい成形の際には満
足できる結果を得ることができても、加工度が大
きくなると、型のかじりや焼付きが生じ、また、
金型の寿命が短くなつて到底満足し得る潤滑処理
方法であるとはいえなかつた。
本発明は、かかる観点に鑑みて創案されたもの
で、300〜800℃の温間域で優れた潤滑性能を発揮
し、加工時に発生する新生面への追従性に優れて
いて型のかじりや焼付きを引起こすことがほとん
どない潤滑被膜を形成することができる金属材料
の温間鍛造用潤滑処理方法を提供するものであ
る。
[問題点を解決するための手段]
すなわち、本発明は、金属材料の温間鍛造に先
駆けて、電着塗装によつて金属材料の表面に、水
溶液中でイオン解離可能な極性基を有する水溶性
又は水分散性の電着樹脂と潤滑性固体粉末とを含
有する潤滑被膜を形成せしめる金属材料の温間鍛
造用潤滑処理方法である。
本発明方法によつて潤滑処理される金属材料と
しては、それが温間鍛造の対象になり、かつ、電
着塗装の手段によつて塗装され得るものであれば
特に制限はなく、例えば、機械構造用鋼、ステン
レス鋼、チタン、各種合金等を挙げることができ
る。
本発明方法においては、上記金属材料の温間鍛
造に先駆けてその表面に、水溶液中でイオン解離
可能な極性基を有する水溶性又は水分散性の電着
樹脂と潤滑性固体粉末とを含有する潤滑被膜を形
成する。
本発明方法で使用する水溶液中でイオン解離可
能な極性基を有する水溶性又は水分散性の電着樹
脂は、例えばカルボキシル基、アミノ基、アミド
基、スルフオン基等の極性基を有し、適当な酸又
は塩基で中和することにより水溶性あるいは水分
散性となつて電気泳動性を示す樹脂であればよ
い。このような電着樹脂としては、例えば、乾性
油、アクリル系樹脂、アルキツド系樹脂、アクリ
ルアルキツド系樹脂、エポキシ系樹脂、アクリル
エポキシ系樹脂、メラミン系樹脂、アクリルメラ
ミン系樹脂、フエノール系樹脂、アクリルフエノ
ール系樹脂、アクリル尿素系樹脂、アクリル変性
ポリエステル系樹脂、ベンゾグアナミン系樹脂、
アミド系樹脂、エステル系樹脂、ウレタン系樹脂
をアニオン化変性したもの又はカチオン化変性し
たものを挙げることができ、陰イオン型であつて
も、また、陽イオン型であつても使用できる。こ
れらの電着樹脂はその1種のみを単独で使用でき
るほか、同種のイオン型であれば2種以上の混合
物として使用することもできる。また、この電着
樹脂を水溶性あるいは水分散性にするための酸と
しては塩酸等の鉱酸又は酢酸等の有機酸を使用す
ることができ、また、塩基としてはアルカリ、ア
ンモニアのほか、エチルアミン、ジメチルアミノ
プロピルアミン、モノエタールアミン、ジメチル
モルホリン等の有機アミンを挙げることができ
る。
また、本発明方法で使用する潤滑剤において、
潤滑性固体粉末としては、その使用温度及び潤滑
面での塑性圧の下で層状に滑るものや使用温度で
溶融して潤滑性能を発揮するものであれば如何な
るものであつてもよく、代表的には結晶構造とし
て最密六方晶系に属するものや層状構造を有する
もの等を挙げることができる。この潤滑性固体粉
末の具体例としては、例えば、黒鉛、弗化黒鉛、
窒化硼素、マイカ、タルク、二硫化タングステ
ン、ガラス、ロウ石、二硫化モリブデン、酸化チ
タン、テフロン、無機燐酸塩、硫化亜鉛等を挙げ
ることができ、これらはその1種のみを単独で使
用できるほか、2種以上の混合物としても使用で
きる。これらの潤滑性固体粉末として好ましいも
のは、黒鉛又はこの黒鉛と他の潤滑性固体粉末の
1種又は2種以上の混合物である。
上記潤滑性固体粉末については、好ましくはそ
の表面を樹脂で被覆した樹脂被覆潤滑性固体粉末
として使用することであり、より好ましくはこの
潤滑性固体粉末の表面を被覆する被覆樹脂として
水溶液中でイオン解離可能な極性基を有する水溶
性又は水分散樹脂、好ましくはアクリル酸、メタ
クリル酸、アレイン酸、イタコン酸、アクリルア
ミド等の少なくとも1つとビニル系モノマーとの
共重合体からなる樹脂を使用することである。
上記潤滑性固体粉末の表面を樹脂で被覆する方
法としては、従来一般に知られている界面重合
法、in situ重合法、液中硬化被覆法、水溶液か
らの相分離法、有機溶液からの相分離法、液中乾
燥法、融解分散冷却法、内包物交換法、粉床法、
気中懸濁被覆法、スプレードライング法、真空蒸
着法、静電合体法等があるが、好ましくは潤滑性
固体粉末の表面に電荷を付与し得る金属塩や有機
物を吸着させた後、この金属塩や有機物と反対の
電荷を有する熱可塑性樹脂ラテツクスの1種又は
2種以上を含有する樹脂溶液又は分散液に接触さ
せる方法であり、より好ましくは潤滑性固体粉末
の表面にビニル系単量体をグラフト重合させる方
法である。
上記潤滑性固体粉末の表面にビニル系単量体を
グラフト重合させる方法としては、ラジカル重合
開始剤の存在下で種々の重合法、例えば、塊状重
合法、溶液重合法等で行うことができるが、亜硫
酸イオンを生成せしめる化合物の存在下に水性媒
質中で潤滑性固体粉末とビニル系単量体とを懸濁
重合させる方法が特に好ましく、また、懸濁重合
の媒質としては水が一般的であるが、これに限定
されず水とメタノールとの混合物等他の水性媒質
を用いることができる。また、懸濁重合における
重合開始剤としては、水性媒質中において亜硫酸
水素イオンを生成せしめる化合物、例えば、二酸
化イオウガスの吹込み、亜硫酸水溶液、あるい
は、亜硫酸水素ソーダ、亜硫酸水素アンモン等の
亜硫酸塩、さらには、過硫酸カリウム、過硫酸ナ
トリウム過硫酸アンモニウム等の過硫酸塩等を単
独又は混合して用いることができる。
この潤滑性固体粉末の表面にビニル系単量体を
グラフト重合させる方法の好ましい態様として
は、潤滑性固体粉末を予め界面活性剤で処理して
この潤滑性固体粉末の表面に選択的な重合の場と
なる界面活性剤の分子層を形成せしめ、次いで液
体分散媒中の潤滑性固体粉末の表面にビニル系単
量体を重合させることにより、潤滑性固体粉末表
面の全部又は大部分をビニル系ポリマーで被覆す
るのがよい。
上記液体分散媒中で潤滑性固体粉末と接触し、
その表面に選択的な重合場となる分子層を形成す
る界面活性剤としては、通常界面活性剤として使
用されているほとんどのものを使用することがで
きる。
また、上記潤滑性固体粉末の表面で重合してこ
の潤滑性固体粉末の表面を被覆するビニル系単量
体としては、アクリル酸、メタクリル酸、α―ク
ロルアクリル酸、イタコン酸、無水マレイン酸、
マレイン酸、フマル酸等の不飽和カルボン酸等の
イオン解離性ビニル系単量体や、塩化ビニル、フ
ツ化ビニルのようなハロゲン化ビニルや、スチレ
ン、α―メチルスチレンのようなスチレン化合
物、酢酸ビニル、プロピオン酸ビニルのような脂
肪族ビニルエステルや、アクリル酸メチル、メタ
クリル酸メチル、グリシジルメタクリレート、メ
タクリル酸ラウリルのような不飽和カルボン酸エ
ステル等の非イオン解離性ビニル系単量体を挙げ
ることができ、好ましくは水溶液中でイオン解離
可能な極性基を有する水溶性又は水分散性樹脂、
例えばアクリル酸、メタクリル酸、マレイン酸、
イタコン酸、アクリルアミド等の少なくとも1つ
とビニル系モノマーとの共重合体からなる樹脂を
生成するビニル系単量体を挙げることができる。
この潤滑性固体粉末の表面にグラフト重合により
樹脂を被覆させる際の樹脂量は、被覆樹脂が水溶
液中でイオン解離可能な極性基を有する水溶性又
は水分散性樹脂である場合には0.1〜75重量%、
好ましくは0.5〜50重量%であり、被覆樹脂が上
記水溶性又は水分散性樹脂でない場合には通常
0.1〜30重量%、好ましくは0.5〜20重量%であ
る。
本発明において、上記電着樹脂と潤滑性固体粉
末との配合割合は、使用する電着樹脂及び潤滑性
固体粉末の種類あるいはこの潤滑性固体粉末が樹
脂被覆されているか否か及びこの被覆樹脂の種類
等によつて異なるが、潤滑性固体粉末100重量部
に対して電着樹脂が10〜300重量部、好ましくは
20〜200重量部である。この電着樹脂の使用量が
10重量部より少ないと金属材料の表面に形成され
る潤滑被膜の強度が不足して円滑な温間鍛造を行
い得なくなり、また、300重量部より多くなると
金属材料の表面に形成される潤滑被膜の潤滑特性
が樹脂によつて支配され、潤滑性固体粉末を使用
する特徴が減少する。なお、潤滑性固体粉末の被
覆樹脂として水溶液中でイオン解離可能な極性基
を有する水溶性又は水分解性樹脂を使用した場合
であつてその樹脂量が10〜75重量%の範囲にある
場合には、この被覆樹脂が電着樹脂としての作用
もするので、特に上記電着樹脂を別個に使用しな
くてもよい。
本発明において、金属材料の表面に上記電着樹
脂と潤滑性固体粉末とを含有する潤滑被膜を形成
する電着塗装方法については、従来一般に行なわ
れている方法でよく、上記電着樹脂と潤滑性固体
粉末とを適当な酸又は塩基及び必要に応じて6価
のクロム酸塩を使用して水に溶解又は分散させて
電着液を調製し、電着樹脂が水溶液中で陰イオン
に解離する場合には金属材料側を陽極にし、ま
た、陽イオンに解離する場合には金属材料側を陰
極にして行う。なお、被加工材となる金属材料の
電着塗装処理を行う前にこの金属材料のスケール
除去や脱脂等が必要であり、このために通常よく
行なわれている各種の洗浄方法、例えば酸洗、ト
リクロロエチレン蒸気脱脂洗浄、超音波洗浄、ブ
ラスト洗浄等を採用することができる。
この電着塗装の際の条件は、電着液中の固形分
濃度が通常3〜50重量%、好ましくは5〜30重量
%であり、電着液のPHについては、アニオン型の
場合は好ましくは7.5〜8.5であつて、カチオン型
の場合は好ましくは5.5〜6.9であり、電着液温度
は10〜90℃、好ましくは30〜80℃であり、電圧は
50〜300V、好ましくは70〜250Vであり、通電時
間は5〜240秒、好ましくは10〜180秒である。こ
れら電着液の固形分濃度、電着液温度、電圧、通
電時間等を適宜変えることにより、金属材料の表
面に形成される潤滑被膜の膜厚を調製することが
できる。この金属材料の表面に形成する潤滑被膜
の膜厚は、通常5〜300μm、好ましくは10〜
150μmの範囲がよい。
[作用]
本発明方法によれば、金属材料の表面に電着樹
脂と潤滑性固体粉末とを含有する潤滑被膜を電着
塗装によつて形成しているので、この金属材料の
表面に電着樹脂が直接強固に化学結合し、しか
も、併用している潤滑性固体粉末がこの電着樹脂
中に取り込まれ、金属材料の表面で極めて強固な
潤滑被膜を形成しているものと考えられる。
[実施例]
以下、実施例及び比較例に基づいて、本発明方
法を具体的に説明する。
実施例 1
平均粒径約2μmの黒鉛粉末100重量部を水1000
重量部中に懸濁させ、これにブチルアクリレート
とアクリル酸とを重量比3:1の割合で混合した
アクリル系単量体50重量部と6wt%亜硫酸水溶液
80重量部とを加え、60℃で5時間撹拌しながら反
応させ、濾過、水洗した後乾燥し、黒鉛の表面に
ブチルアクリレート・アクリル酸コポリマーが被
覆した樹脂量31重量%の樹脂被覆黒鉛粉末145重
量部を得た。
次に、得られた樹脂被覆黒鉛粉末100重量部を
水1000重量部に懸濁し、アンモニア水でPH7.5に
調整して電着液とした。この電着液を使用し、直
径30mm×高さ45mmの被加工材である金属材料(材
質S45C)を陽極とし、ステンレス鋼板
(SUS304)を陰極として電着塗装を行い、金属
材料の表面に膜厚60μmの潤滑被膜を形成した。
この潤滑被膜の黒鉛含有率は68重量%であつた。
このようにして被加工材の金属材料を潤滑処理
した後、この被加工材を高周波で550℃及び700℃
に加熱し、200tonプレスでそれぞれ145ton及び
70tonかけた時の被加工材の最大直径を第1表に
示す。被加工材における潤滑被膜の膜切れや金型
焼付きがなく、プレスによる温間鍛造を極めて円
滑に行うことができた。
実施例 2
平均粒径約2μmの黒鉛粉末100重量部を水1000
重量部中に懸濁させ、これにメチルメタクリレー
ト単量体5重量部と6wt%亜硫酸水溶液20重量部
とを加え、60℃で3時間撹拌しながら反応させ、
濾過、水洗した後乾燥し、黒鉛の表面にメチルメ
タクリレート樹脂が被覆した樹脂量4.7重量%の
樹脂被覆黒鉛粉末105重量部を得た。
次に、得られた樹脂被覆黒鉛粉末50重量部とア
クリル系アニオン型電着樹脂(東亜合成(株)製商品
名:アロンS4020)100重量部とを水1000重量部
に懸濁し、アンモニア水でPH7.5に調整して電着
液とした。この電着液を使用し実施例1と同様に
して電着塗装を行い、金属材料の表面に膜厚40μ
mの潤滑被膜を形成した。この潤滑被膜の黒鉛含
有率は63重量%であつた。
このようにして潤滑処理した被加工材につい
て、上記実施例1と同様の条件でプレス加工を行
つた。被加工材の加工後の最大直径を第1表に示
す。被加工材における潤滑被膜の膜切れや金型焼
付きがなく、プレスによる温間鍛造を極めて円滑
に行うことができた。
実施例 3
平均粒径約2μmの黒鉛粉末50重量部と実施例
2で使用したアクリル系アニオン型電着樹脂100
重量部とを水1000重量部に懸濁し、アンモニア水
でPH7.5に調整して電着液とした。この電着液を
使用し実施例1と同様にして電着塗装を行い、金
属材料の表面に膜厚30μmの潤滑被膜を形成し
た。この潤滑被膜の黒鉛含有率は60重量%であつ
た。
このようにして潤滑処理した被加工材につい
て、上記実施例1と同様の条件でプレス加工を行
つた。被加工材の加工後の最大直径を第1表に示
す。被加工材における潤滑被膜の膜切れや金型焼
付きがなく、プレスによる温間鍛造を極めて円滑
に行うことができた。
実施例 4
平均粒径約6μmの窒化硼素粉末50重量部とア
ルキツド樹脂(大日本インキ(株)製商品名:ウオー
ターゾールS―136)100重量部とを使用し、実施
例3と同様にして電着液とした。この電着液を使
用し実施例1と同様にして電着塗装を行い、金属
材料の表面に膜厚15μmの潤滑被膜を形成した。
この潤滑被膜の窒化硼素含有率は50重量%であつ
た。
このようにして潤滑処理した被加工材につい
て、上記実施例1と同様の条件でプレス加工を行
つた。被加工材の加工後の最大直径を第1表に示
す。被加工材における潤滑被膜の膜切れや金型焼
付きがなく、プレスによる温間鍛造を極めて円滑
に行うことができた。
比較例 1
実施例1で調製した電着液中に実施例1で使用
した被加工材を浸漬したところ付着が不十分であ
つたので、実施例1の電着液をエアスプレーで実
施例1の被加工材に塗布してその表面に膜厚60μ
mの潤滑被膜を形成し、実施例1と同様の条件で
プレス成形を行つた。被加工材の加工後の最大直
径を第1表に示す。この時、被加工材における潤
滑被膜の膜切れが一部発生し、金型への焼付きが
認められた。
比較例 2
実施例2で調製した電着液中に実施例1で使用
した被加工材を浸漬してその表面に膜厚40μmの
潤滑被膜を形成し、実施例1と同様の条件でプレ
ス成形を行つた。被加工材の加工後の最大直径を
第1表に示す。この時、被加工材における潤滑被
膜の膜切れが発生し、金型への焼付きが認められ
た。
比較例 3
実施例3で調製した電着液中に実施例1で使用
した被加工材を浸漬してその表面に膜厚30μmの
潤滑被膜を形成し、実施例1と同様の条件でプレ
ス成形を行つた。被加工材の加工後の最大直径を
第1表に示す。この時、被加工材における潤滑被
膜の膜切れが発生し、金型への焼付きが認められ
た。
比較例 4
実施例4で調製した電着液中に実施例1で使用
した被加工材を浸漬してその表面に膜厚15μmの
潤滑被膜を形成し、実施例1と同様の条件でプレ
ス成形を行つた。被加工材の加工後の最大直径を
第1表に示す。この時、被加工材における潤滑被
膜の膜切れが発生し、金型への焼付きが認められ
た。
[Industrial Application Field] This invention is applied as a pre-treatment when manufacturing various parts of automobiles, construction machines, agricultural machinery, etc., parts of various tools, various parts of electrical equipment, etc. by warm forging. This invention relates to a lubrication treatment method. [Prior art] There are three known forging methods for forging metal materials: cold, warm, and hot, and the advantages and disadvantages of each have been reported in many documents. However, for machining that requires precision, warm forging is said to be the most superior in terms of quality and energy. When carrying out this warm forging, the surface of the metal material is lubricated as a pretreatment, but in the past, the metal material was immersed in an aqueous or oil dispersion of a solid lubricant. This metal material is coated with an aqueous dispersion or an oil dispersion of the solid lubricant by spraying or the like. [Problems to be solved by the invention] However, in the above conventional lubrication treatment method,
If the strength of the lubricating film formed on the surface of the metal material is insufficient, or if the solid lubricant is not sufficiently introduced to the new surface during warm forging, it may be difficult to obtain satisfactory results when forming with a small degree of processing. Even if it is possible, if the degree of processing increases, galling and seizure of the mold will occur, and
Since the life of the mold was shortened, it could not be said that this was a completely satisfactory lubrication method. The present invention was devised in view of these points of view, and exhibits excellent lubrication performance in the warm range of 300 to 800°C, and has excellent followability to new surfaces generated during processing, preventing mold galling and burning. The present invention provides a lubrication treatment method for warm forging of metal materials that can form a lubricant film that hardly causes sticking. [Means for Solving the Problems] That is, the present invention provides, prior to warm forging of a metal material, applying a water-soluble material having a polar group that can be ionically dissociated in an aqueous solution to the surface of the metal material by electrodeposition. This is a lubrication treatment method for warm forging of metal materials, which forms a lubricating film containing a water-dispersible electrodeposited resin and a lubricating solid powder. The metal material to be lubricated by the method of the present invention is not particularly limited as long as it can be subjected to warm forging and can be coated by electrocoating. Structural steel, stainless steel, titanium, various alloys, etc. can be mentioned. In the method of the present invention, prior to warm forging of the metal material, a water-soluble or water-dispersible electrodeposited resin having a polar group that can be ionically dissociated in an aqueous solution and a lubricating solid powder are contained on the surface of the metal material. Forms a lubricating film. The water-soluble or water-dispersible electrodeposited resin having a polar group that is ionically dissociable in an aqueous solution used in the method of the present invention has a polar group such as a carboxyl group, an amino group, an amide group, a sulfonate group, etc. Any resin may be used as long as it becomes water-soluble or water-dispersible when neutralized with an acid or base and exhibits electrophoretic properties. Examples of such electrodeposition resin include drying oil, acrylic resin, alkyd resin, acrylic alkyd resin, epoxy resin, acrylic epoxy resin, melamine resin, acrylic melamine resin, phenol resin, Acrylic phenol resin, acrylic urea resin, acrylic modified polyester resin, benzoguanamine resin,
Examples include anionically modified or cationically modified amide resins, ester resins, and urethane resins, and both anionic and cationic types can be used. These electrodeposited resins can be used alone or in a mixture of two or more of the same ionic type. In addition, mineral acids such as hydrochloric acid or organic acids such as acetic acid can be used as acids to make this electrodeposited resin water-soluble or water-dispersible, and bases include alkalis, ammonia, and ethylamine. , dimethylaminopropylamine, monoethalamine, dimethylmorpholine, and other organic amines. Furthermore, in the lubricant used in the method of the present invention,
The lubricating solid powder may be of any kind as long as it slides in a layered manner under the operating temperature and plastic pressure on the lubricated surface, or that melts at the operating temperature and exhibits lubricating performance. Examples of the crystal structure include those belonging to a close-packed hexagonal system and those having a layered structure. Specific examples of this lubricating solid powder include graphite, fluorinated graphite,
Examples include boron nitride, mica, talc, tungsten disulfide, glass, waxite, molybdenum disulfide, titanium oxide, Teflon, inorganic phosphates, zinc sulfide, etc., and only one of these can be used alone. , it can also be used as a mixture of two or more types. Preferred as these lubricating solid powders are graphite or a mixture of one or more of graphite and other lubricating solid powders. The above-mentioned lubricating solid powder is preferably used as a resin-coated lubricating solid powder whose surface is coated with a resin, and more preferably, it is used as a resin-coated lubricating solid powder that coats the surface of this lubricating solid powder with ions in an aqueous solution. By using a water-soluble or water-dispersible resin having a dissociable polar group, preferably a resin consisting of a copolymer of at least one of acrylic acid, methacrylic acid, areic acid, itaconic acid, acrylamide, etc. and a vinyl monomer. be. Methods for coating the surface of the above-mentioned lubricating solid powder with resin include the conventionally known interfacial polymerization method, in situ polymerization method, in-liquid curing coating method, phase separation method from an aqueous solution, and phase separation method from an organic solution. method, submerged drying method, melting dispersion cooling method, inclusion exchange method, powder bed method,
There are air suspension coating methods, spray drying methods, vacuum evaporation methods, electrostatic coalescence methods, etc., but preferably after adsorbing a metal salt or organic substance that can impart an electric charge to the surface of a lubricating solid powder, this metal This is a method in which the lubricating solid powder is brought into contact with a resin solution or dispersion containing one or more types of thermoplastic resin latex having a charge opposite to that of a salt or an organic substance, and more preferably a vinyl monomer is added to the surface of the lubricating solid powder. This is a method of graft polymerizing. Graft polymerization of the vinyl monomer onto the surface of the above-mentioned lubricating solid powder can be carried out by various polymerization methods such as bulk polymerization method and solution polymerization method in the presence of a radical polymerization initiator. Particularly preferred is a method in which a lubricating solid powder and a vinyl monomer are subjected to suspension polymerization in an aqueous medium in the presence of a compound that generates sulfite ions, and water is generally used as the medium for suspension polymerization. Other aqueous media can be used, such as, but not limited to, a mixture of water and methanol. In addition, as a polymerization initiator in suspension polymerization, a compound that generates hydrogen sulfite ions in an aqueous medium, such as the injection of sulfur dioxide gas, an aqueous solution of sulfite, or a sulfite such as sodium hydrogen sulfite or ammonium hydrogen sulfite; Persulfates such as potassium persulfate, sodium persulfate and ammonium persulfate can be used alone or in combination. A preferred embodiment of the method for graft polymerizing the vinyl monomer onto the surface of this lubricating solid powder is to treat the lubricating solid powder with a surfactant in advance to selectively polymerize the surface of the lubricating solid powder. By forming a molecular layer of a surfactant that acts as a field, and then polymerizing a vinyl monomer on the surface of the lubricating solid powder in the liquid dispersion medium, all or most of the surface of the lubricating solid powder is made of vinyl. It is better to coat it with a polymer. contacting the lubricating solid powder in the liquid dispersion medium;
As the surfactant that forms a molecular layer on the surface that serves as a selective polymerization site, most of the surfactants commonly used can be used. In addition, examples of vinyl monomers that polymerize on the surface of the lubricating solid powder to coat the surface of the lubricating solid powder include acrylic acid, methacrylic acid, α-chloroacrylic acid, itaconic acid, maleic anhydride,
Ionically dissociable vinyl monomers such as unsaturated carboxylic acids such as maleic acid and fumaric acid, vinyl halides such as vinyl chloride and vinyl fluoride, styrene compounds such as styrene and α-methylstyrene, and acetic acid. Nonionically dissociable vinyl monomers such as vinyl, aliphatic vinyl esters such as vinyl propionate, and unsaturated carboxylic acid esters such as methyl acrylate, methyl methacrylate, glycidyl methacrylate, and lauryl methacrylate. water-soluble or water-dispersible resin, preferably having a polar group that can be ionically dissociated in an aqueous solution;
For example, acrylic acid, methacrylic acid, maleic acid,
Examples include vinyl monomers that produce resins consisting of copolymers of at least one of itaconic acid, acrylamide, etc., and vinyl monomers.
When coating the surface of this lubricating solid powder with resin by graft polymerization, the amount of resin is 0.1 to 75% when the coating resin is a water-soluble or water-dispersible resin having a polar group that can be ionically dissociated in an aqueous solution. weight%,
Preferably it is 0.5 to 50% by weight, and when the coating resin is not the water-soluble or water-dispersible resin mentioned above, it is usually
0.1-30% by weight, preferably 0.5-20% by weight. In the present invention, the blending ratio of the electrocoated resin and the lubricating solid powder is determined by the types of the electrocoated resin and lubricating solid powder used, whether or not the lubricating solid powder is coated with a resin, and whether or not the lubricating solid powder is coated with a resin. Although it varies depending on the type etc., 10 to 300 parts by weight of the electrodeposited resin is preferably added to 100 parts by weight of the lubricating solid powder.
20 to 200 parts by weight. The amount of this electrodeposition resin used is
If it is less than 10 parts by weight, the strength of the lubricating film formed on the surface of the metal material will be insufficient and smooth warm forging will not be possible, and if it is more than 300 parts by weight, the lubricating film formed on the surface of the metal material will be insufficient. The lubricating properties of the resin are dominated by the resin, reducing the characteristics of using lubricating solid powders. In addition, when a water-soluble or water-decomposable resin having a polar group that can be ionically dissociated in an aqueous solution is used as the coating resin for the lubricating solid powder, and the amount of the resin is in the range of 10 to 75% by weight, Since this coating resin also acts as an electrodeposition resin, there is no need to use the electrodeposition resin separately. In the present invention, the electrodeposition coating method for forming a lubricating film containing the electrodeposition resin and the lubricating solid powder on the surface of the metal material may be any conventionally commonly used method. An electrodeposition solution is prepared by dissolving or dispersing the solid powder in water using a suitable acid or base and, if necessary, hexavalent chromate, and the electrodeposition resin dissociates into anions in the aqueous solution. When dissociating into cations, the metal material side is used as an anode, and when dissociating into cations, the metal material side is used as a cathode. It should be noted that before the metal material to be processed is subjected to electrodeposition coating, it is necessary to remove scale and degrease the metal material, and for this purpose various commonly used cleaning methods such as pickling, pickling, etc. Trichlorethylene vapor degreasing cleaning, ultrasonic cleaning, blast cleaning, etc. can be employed. The conditions for this electrodeposition coating are that the solid content concentration in the electrodeposition liquid is usually 3 to 50% by weight, preferably 5 to 30% by weight, and the pH of the electrodeposition liquid is preferably anionic. is 7.5 to 8.5, preferably 5.5 to 6.9 in the case of cationic type, the electrodeposition liquid temperature is 10 to 90°C, preferably 30 to 80°C, and the voltage is
The voltage is 50 to 300V, preferably 70 to 250V, and the current application time is 5 to 240 seconds, preferably 10 to 180 seconds. The thickness of the lubricating film formed on the surface of the metal material can be adjusted by appropriately changing the solid content concentration, electrodeposition liquid temperature, voltage, current application time, etc. of the electrodeposition liquid. The thickness of the lubricating film formed on the surface of this metal material is usually 5 to 300 μm, preferably 10 to 300 μm.
A range of 150 μm is preferable. [Function] According to the method of the present invention, since a lubricating film containing an electrodeposited resin and a lubricating solid powder is formed on the surface of a metal material by electrodeposition coating, the surface of the metal material cannot be electrodeposited. It is thought that the resin is directly and strongly chemically bonded, and that the lubricating solid powder used in combination is incorporated into this electrodeposited resin, forming an extremely strong lubricating film on the surface of the metal material. [Example] Hereinafter, the method of the present invention will be specifically explained based on Examples and Comparative Examples. Example 1 100 parts by weight of graphite powder with an average particle size of about 2 μm was added to 100 parts by weight of water.
50 parts by weight of an acrylic monomer and 6 wt% sulfite aqueous solution, which is suspended in 1 part by weight and mixed with butyl acrylate and acrylic acid at a weight ratio of 3:1.
80 parts by weight was added, reacted with stirring at 60°C for 5 hours, filtered, washed with water, and dried to obtain resin-coated graphite powder 145 with a resin content of 31% by weight, in which the surface of the graphite was coated with butyl acrylate/acrylic acid copolymer. Parts by weight were obtained. Next, 100 parts by weight of the obtained resin-coated graphite powder was suspended in 1000 parts by weight of water, and the pH was adjusted to 7.5 with aqueous ammonia to prepare an electrodeposition liquid. Using this electrodeposition solution, electrodeposition is performed using a metal material (material S45C) as an anode and a stainless steel plate (SUS304) as a workpiece with a diameter of 30 mm x height of 45 mm as a cathode, and a film is applied to the surface of the metal material. A lubricating film with a thickness of 60 μm was formed.
The graphite content of this lubricating coating was 68% by weight. After lubricating the metal material of the workpiece in this way, the workpiece is heated to 550°C and 700°C by high frequency.
heated to 145ton and 200ton press respectively.
Table 1 shows the maximum diameter of the workpiece when 70 tons is applied. There was no breakage of the lubricating film on the workpiece or seizure of the mold, and warm forging using a press could be performed extremely smoothly. Example 2 100 parts by weight of graphite powder with an average particle size of about 2 μm was mixed with 100 parts by weight of water.
5 parts by weight of methyl methacrylate monomer and 20 parts by weight of 6 wt% sulfite aqueous solution were added thereto, and the mixture was reacted with stirring at 60°C for 3 hours.
After filtering, washing with water, and drying, 105 parts by weight of resin-coated graphite powder with a resin amount of 4.7% by weight, in which the surface of the graphite was coated with methyl methacrylate resin, was obtained. Next, 50 parts by weight of the obtained resin-coated graphite powder and 100 parts by weight of acrylic anionic electrodeposited resin (trade name: Aron S4020, manufactured by Toagosei Co., Ltd.) were suspended in 1000 parts by weight of water, and aqueous ammonia was added. The pH was adjusted to 7.5 and used as an electrodeposition solution. Using this electrodeposition liquid, electrodeposition coating was performed in the same manner as in Example 1, and a film thickness of 40 μm was applied to the surface of the metal material.
A lubricating film of m was formed. The graphite content of this lubricating coating was 63% by weight. The workpiece thus lubricated was subjected to press working under the same conditions as in Example 1 above. Table 1 shows the maximum diameter of the workpiece after processing. There was no breakage of the lubricating film on the workpiece or mold seizure, and warm forging using a press could be performed extremely smoothly. Example 3 50 parts by weight of graphite powder with an average particle size of about 2 μm and 100 parts by weight of the acrylic anionic electrodeposited resin used in Example 2
parts by weight were suspended in 1000 parts by weight of water, and the pH was adjusted to 7.5 with aqueous ammonia to prepare an electrodeposition solution. Electrodeposition coating was performed using this electrodeposition liquid in the same manner as in Example 1 to form a lubricating film with a thickness of 30 μm on the surface of the metal material. The graphite content of this lubricating coating was 60% by weight. The workpiece thus lubricated was subjected to press working under the same conditions as in Example 1 above. Table 1 shows the maximum diameter of the workpiece after processing. There was no breakage of the lubricating film on the workpiece or mold seizure, and warm forging using a press could be performed extremely smoothly. Example 4 The same procedure as in Example 3 was carried out using 50 parts by weight of boron nitride powder with an average particle size of about 6 μm and 100 parts by weight of alkyd resin (trade name: Watersol S-136, manufactured by Dainippon Ink Co., Ltd.). It was used as an electrodeposition liquid. Electrodeposition coating was performed using this electrodeposition liquid in the same manner as in Example 1 to form a lubricating film with a thickness of 15 μm on the surface of the metal material.
The boron nitride content of this lubricating coating was 50% by weight. The workpiece thus lubricated was subjected to press working under the same conditions as in Example 1 above. Table 1 shows the maximum diameter of the workpiece after processing. There was no breakage of the lubricating film on the workpiece or mold seizure, and warm forging using a press could be performed extremely smoothly. Comparative Example 1 When the workpiece used in Example 1 was immersed in the electrodeposition liquid prepared in Example 1, the adhesion was insufficient, so the electrodeposition liquid of Example 1 was air-sprayed into Example 1. It is applied to the workpiece and a film thickness of 60μ is applied to the surface of the workpiece.
A lubricating film of m was formed, and press molding was performed under the same conditions as in Example 1. Table 1 shows the maximum diameter of the workpiece after processing. At this time, some breakage of the lubricating film on the workpiece occurred, and seizure to the mold was observed. Comparative Example 2 The workpiece used in Example 1 was immersed in the electrodeposition liquid prepared in Example 2 to form a lubricating film with a thickness of 40 μm on the surface, and press molded under the same conditions as Example 1. I went there. Table 1 shows the maximum diameter of the workpiece after processing. At this time, breakage of the lubricating film on the workpiece occurred, and seizure to the mold was observed. Comparative Example 3 The workpiece used in Example 1 was immersed in the electrodeposition liquid prepared in Example 3 to form a lubricating film with a thickness of 30 μm on the surface, and press molded under the same conditions as Example 1. I went there. Table 1 shows the maximum diameter of the workpiece after processing. At this time, breakage of the lubricating film on the workpiece occurred, and seizure to the mold was observed. Comparative Example 4 The workpiece used in Example 1 was immersed in the electrodeposition liquid prepared in Example 4 to form a lubricating film with a thickness of 15 μm on the surface, and press molded under the same conditions as Example 1. I went there. Table 1 shows the maximum diameter of the workpiece after processing. At this time, breakage of the lubricating film on the workpiece occurred, and seizure to the mold was observed.
【表】
上記第1表の結果から明らかなように、各実施
例における被加工材の変形量は各比較例の場合に
比べてはるかに大きくなつており、また、潤滑被
膜の膜切れや金型への焼付きも発生しない。
[発明の効果]
本発明の金属材料の温間鍛造用潤滑処理方法に
よれば、300〜800℃の温間域で優れた潤滑性能を
発揮し、成形性が増すと共に加工時に発生する新
生面への追従性に優れていて型のかじりや焼付き
を引起こすことがほとんどない潤滑被膜を形成す
ることができ、金属材料の温間鍛造を容易に行う
ことができるほか、金型の寿命を改善することが
できる。[Table] As is clear from the results in Table 1 above, the amount of deformation of the workpiece in each example was much larger than in each comparative example, and there were also problems such as breakage of the lubricant film and metallurgy. No sticking to the mold occurs. [Effect of the invention] According to the lubrication treatment method for warm forging of metal materials of the present invention, excellent lubrication performance is exhibited in the warm range of 300 to 800°C, and formability is increased and new surfaces generated during processing are prevented. It can form a lubricating film that has excellent followability and hardly causes galling or seizure of the mold, making it easier to perform warm forging of metal materials and improving the life of the mold. can do.
Claims (1)
よつて金属材料の表面に、水溶液中でイオン解離
可能な極性基を有する水溶性又は水分散性の電着
樹脂と潤滑性固体粉末とを含有する潤滑被膜を形
成せしめることを特徴とする金属材料の温間鍛造
用潤滑処理方法。 2 潤滑性固体粉末としてその表面が樹脂被覆さ
れた樹脂被覆潤滑性固体粉末を使用する特許請求
の範囲第1項記載の金属材料の温間鍛造用潤滑処
理方法。 3 潤滑性固体粉末の表面を被覆する被覆樹脂が
水溶液中でイオン解離可能な極性基を有する水溶
性又は水分散性樹脂である特許請求の範囲第2項
記載の金属材料の温間鍛造用潤滑処理方法。[Claims] 1. Prior to warm forging of a metal material, a water-soluble or water-dispersible electrodeposition resin having a polar group that can be ionically dissociated in an aqueous solution is applied to the surface of the metal material by electrodeposition coating. 1. A lubrication treatment method for warm forging of metal materials, the method comprising forming a lubricating film containing a lubricating solid powder and a lubricating solid powder. 2. The lubrication treatment method for warm forging of metal materials according to claim 1, wherein a resin-coated lubricant solid powder whose surface is coated with a resin is used as the lubricant solid powder. 3. Lubrication for warm forging of metal materials according to claim 2, wherein the coating resin that coats the surface of the lubricating solid powder is a water-soluble or water-dispersible resin having a polar group that can be ionically dissociated in an aqueous solution. Processing method.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1110086A JPS62169899A (en) | 1986-01-23 | 1986-01-23 | Method of lubrication treatment for hot forging of metallic material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1110086A JPS62169899A (en) | 1986-01-23 | 1986-01-23 | Method of lubrication treatment for hot forging of metallic material |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS62169899A JPS62169899A (en) | 1987-07-27 |
| JPH04514B2 true JPH04514B2 (en) | 1992-01-07 |
Family
ID=11768587
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1110086A Granted JPS62169899A (en) | 1986-01-23 | 1986-01-23 | Method of lubrication treatment for hot forging of metallic material |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS62169899A (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5468401A (en) * | 1989-06-16 | 1995-11-21 | Chem-Trend, Incorporated | Carrier-free metalworking lubricant and method of making and using same |
| JP2776619B2 (en) * | 1990-06-26 | 1998-07-16 | 株式会社大同機械製作所 | Forging coating lubrication processing method and forging apparatus having coating lubrication processing means |
| CA2052604A1 (en) * | 1991-03-04 | 1992-09-05 | Andrew F. Lum | Carrier-free metalworking lubricant and method of making and using same |
| JP2009040802A (en) * | 2007-08-06 | 2009-02-26 | Matsufumi Takatani | Method for imparting lubricity to surface of substrate and substrate having lubricating surface |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5071561A (en) * | 1973-10-30 | 1975-06-13 | ||
| US4318792A (en) * | 1980-07-07 | 1982-03-09 | Trw Inc. | Process for depositing forging lubricant on titanium workpiece |
| JPS5765795A (en) * | 1980-10-08 | 1982-04-21 | Nippon Steel Corp | Lubricated metallic plate having excellent ddep drawability |
| JPS5765796A (en) * | 1980-10-08 | 1982-04-21 | Nippon Steel Corp | Cold rolling method of steel sheet |
-
1986
- 1986-01-23 JP JP1110086A patent/JPS62169899A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS62169899A (en) | 1987-07-27 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US9539611B2 (en) | Method for coating surfaces and use of the articles coated using said method | |
| US4373050A (en) | Process and composition for coating metals | |
| JP3404286B2 (en) | Metal surface treatment method, and metal member having a surface obtained by the surface treatment method | |
| TWI457433B (en) | Process for coating metallic surfaces with a phosphate layer and then with a polymer lubricant layer | |
| US3795601A (en) | Electrodiffused protective coating system | |
| US4156040A (en) | Coagulation coating process | |
| JPH03219086A (en) | Composition for metal surface treatment excellent in lubricity | |
| CN111471986A (en) | Method for coating a metal surface of a substrate and object coated according to said method | |
| US4086153A (en) | Method of producing a composite coated steel sheet | |
| HK1000650B (en) | Process for plating a face of an aluminium or aluminium alloy workpiece | |
| HK1000650A1 (en) | Process for plating a face of an aluminium or aluminium alloy workpiece | |
| US4136070A (en) | Cathodic electrodeposition of paints | |
| US4104424A (en) | Process for coating metals | |
| US4225407A (en) | Cathodic electrodeposition of polymers onto a conductive surface | |
| US3864230A (en) | Pretreating and Electrocoating Metal Products | |
| JPH0847666A (en) | Metal surface denaturation processing method | |
| JPS62169899A (en) | Method of lubrication treatment for hot forging of metallic material | |
| CN101104946B (en) | Electrolytic phosphating treatment method and warm or hot forging method | |
| IL27166A (en) | Dry lubricant,articles coated therewith and method of making it | |
| JPH0756080B2 (en) | Method for producing organic polymer composite metallurgical metal material with excellent paint adhesion | |
| US4225406A (en) | Cationic deposition of polymers onto a conductive surface | |
| JPH0220336A (en) | Organic coating | |
| US3994792A (en) | Electrodeposition of sulfoxonium stabilized colloids | |
| JPS5928639B2 (en) | Fukugohi Fukukinzokubanno Seizouhouhou | |
| RU2023763C1 (en) | Method of polymeric coating preparing |