JPS60141337A - Production of fin for heat exchanger - Google Patents

Production of fin for heat exchanger

Info

Publication number
JPS60141337A
JPS60141337A JP58245095A JP24509583A JPS60141337A JP S60141337 A JPS60141337 A JP S60141337A JP 58245095 A JP58245095 A JP 58245095A JP 24509583 A JP24509583 A JP 24509583A JP S60141337 A JPS60141337 A JP S60141337A
Authority
JP
Japan
Prior art keywords
fin
heat exchanger
aluminum
film
flare
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
JP58245095A
Other languages
Japanese (ja)
Other versions
JPH024379B2 (en
Inventor
Tetsuji Iwama
岩間 哲治
Tsuyoshi Katsumata
堅 勝又
Koji Mitamura
三田村 康二
Isao Takeuchi
竹内 庸
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.)
MA Aluminum Corp
Original Assignee
Mitsubishi Aluminum 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 Mitsubishi Aluminum Co Ltd filed Critical Mitsubishi Aluminum Co Ltd
Priority to JP58245095A priority Critical patent/JPS60141337A/en
Publication of JPS60141337A publication Critical patent/JPS60141337A/en
Publication of JPH024379B2 publication Critical patent/JPH024379B2/ja
Granted 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
    • C10M101/00Lubricating compositions characterised by the base-material being a mineral or fatty oil
    • C10M101/02Petroleum fractions
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C24/00Coating starting from inorganic powder
    • C23C24/08Coating starting from inorganic powder by application of heat or pressure and heat
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C28/00Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Metal Extraction Processes (AREA)
  • Shaping Metal By Deep-Drawing, Or The Like (AREA)

Abstract

PURPOSE:To eliminate deterioration in corrosion resistance and heat exchangeability of heat exchanging fins by coating a lubricating material consisting of a base material composed of paraffinic and naphthenic hydrocarbons on an aluminum sheet having an org. or inorg. film, activating the same by heating and pressing the aluminum sheet. CONSTITUTION:A mixture composed essentially of paraffinic hydrocarbon and naphthenic hydrocarbon having 15-20 average number of carbon atoms and 200-350 average mol.wt. is coated on the surface of an expanded aluminum or aliminum alloy sheet having an org. or inorg. film at 1-8mg/dm<2> coating amt., <=150ppm moisture concn. and 5-10cst viscosity. The aluminum sheet is heated to 50-200 deg.C surface temp. to activate the lubricating material then the aluminum sheet is pressed. Flare drop-out and flare crack are thus prevented and the deterioration in the corrosion resistance and heat exchangeability of the heat exchanging fins is prevented.

Description

【発明の詳細な説明】 本発明は家庭用冷熱機器や自動車等の熱交換器フィンさ
れる熱交換器用フィン材の製造方法(以下単にフイ/の
−造方法と記載する。)に係るものであり、アルミニウ
ム又はアルミニウム合金板(以下単にアルミニウム板と
記載する。)の表面に無機質又は有機質の皮膜又はそれ
らの複合された皮膜を設けた後で該板体をドローレスプ
レス加工する際に、成形性が良く、耐食性のある、熱交
換効率の優れた熱交換器用フィンを大量に供給テキルフ
ィンの製造法に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for manufacturing a fin material for a heat exchanger (hereinafter simply referred to as a fin manufacturing method) for use in heat exchanger fins for household cooling and heating equipment, automobiles, etc. Yes, after providing an inorganic or organic film or a composite film of these on the surface of an aluminum or aluminum alloy plate (hereinafter simply referred to as an aluminum plate), the formability is improved when the plate is subjected to drawless press processing. The present invention relates to a method for manufacturing fins for heat exchangers, which provides a large quantity of fins for heat exchangers that have good corrosion resistance, excellent heat exchange efficiency, and excellent heat exchange efficiency.

従来アルミニウム板は上記した如く表面処理を施した後
、例えばドローレスプレス加工をして熱交換器用フィン
1[造する場合に於いて、プレス加工時に、フレアー飛
びあるいはフレアー割れと称する事故が起り、しばしば
熱交換部材としての耐食性、熱交換率などの性能を低下
させ、はなはだしい場合には、使用に耐えなくなる場合
があった。
Conventionally, aluminum plates have been subjected to surface treatment as described above, and then subjected to drawless press processing to produce heat exchanger fins 1. However, during press processing, an accident called flare flying or flare cracking often occurs. Performance as a heat exchange member such as corrosion resistance and heat exchange rate deteriorates, and in extreme cases, it may become unusable.

本発明者等は上記欠陥につき種々検討する段階で、アル
ミニウム板表面に付着する炭化水素化合物さらに研究の
結果、本発明に到達したものでありその要旨とするとこ
ろは、アルミニウム板表面に、例、t Id、ベーマイ
ト皮膜、クロメート皮膜、陽極酸化皮膜、その他の手段
によって化成した無機皮膜、あるいは有機高分子、又は
無機−有機高分子等を塗布することによる保護皮膜が形
成されている表面上に予めプレス加工に先だって脂肪族
炭化水素中パラフィン系4!F#童−、− 炭化水素(CnHzn+2 ) 、ナフテン系炭化水素
形プレス直前に於いて熱風、スチーム加熱等によりて該
・・板□、を「加1熱することにより、塗布されている
パラフィン系又はナフテン系炭化水素が活性化される。
The inventors of the present invention were at the stage of various studies regarding the above-mentioned defects, and as a result of further research into hydrocarbon compounds adhering to the surface of an aluminum plate, they arrived at the present invention. t Id, a boehmite film, a chromate film, an anodized film, an inorganic film chemically formed by other means, an organic polymer, or an inorganic-organic polymer, etc. on the surface that has been previously formed with a protective film. Paraffinic in aliphatic hydrocarbons prior to pressing 4! F# -, - hydrocarbon (CnHzn+2), naphthenic hydrocarbon type.By heating the plate □ with hot air, steam heating, etc. immediately before pressing, the applied paraffin type Or naphthenic hydrocarbons are activated.

この状態で、プレス作業を行うとアルミニ・ラム・・板
、等の表面が活性化されているので境界潤滑が良好とな
り、フレアー飛び、フレアー割れ等の事故のない良好な
フィンを得ることが出来る。
When press work is performed in this state, the surface of the aluminum, ram, plate, etc. is activated, so boundary lubrication is good, and good fins can be obtained without accidents such as flare flying and flare cracking. .

尚この活性化の方法は加熱による方法に限るものではな
い。また、本発明に使用される潤滑剤の組成は、脂肪族
炭化水素が主体であるが、原料等の違いにより、組成及
び平均分子量が多少異なる場合もあるが、主成分は上記
したようにパラフィン系炭化水素、ナフテン系炭化水素
を中心とする組成である。すなわち、これら主成分の割
合は、例えば50:50でも、30ニア0でもまたはこ
の逆でもよく特に限定の必要はないが平均分子量は20
0〜350であり、平均炭素数(n)が15〜25の範
囲のものがよい。また粘度は使用条件により興なるが通
常の使用状態では40℃に於ける粘度は5〜10 es
tの範囲のものが使われる。また本欄滑剤中には耐摩性
添加剤が5チ以下含有されてもよく、含有水分は保存性
及び処理板への耐食性の影響の点から156 ppm以
下に押えた方がよい。
Note that this activation method is not limited to the method using heating. In addition, the composition of the lubricant used in the present invention is mainly composed of aliphatic hydrocarbons, but the composition and average molecular weight may differ slightly depending on the raw materials, etc., but the main component is paraffin as described above. The composition is mainly composed of naphthenic hydrocarbons and naphthenic hydrocarbons. That is, the ratio of these main components may be, for example, 50:50, 30:0, or vice versa, and is not particularly limited, but the average molecular weight is 20:0.
0 to 350, and preferably has an average carbon number (n) of 15 to 25. Also, the viscosity varies depending on the usage conditions, but under normal usage conditions, the viscosity at 40°C is 5 to 10 es.
A range of t is used. In addition, the lubricant in this column may contain up to 5 parts of wear-resistant additives, and the water content should be kept to 156 ppm or less in view of storage stability and corrosion resistance of treated plates.

以下本発明の限定理由につき記述する。The reasons for the limitations of the present invention will be described below.

本発明処理法に用いられる潤滑剤の主成分をパラフィン
系及びナフテン系の炭化水素で平均分子量を200〜3
50とし、平均炭素数が15〜25としたのは、それ以
下では成形プレス直前に於いて加熱した際に潤滑剤が流
れ落ちてしまい、またそれ以上では加熱後の流動性に欠
けるためである。
The main components of the lubricant used in the treatment method of the present invention are paraffinic and naphthenic hydrocarbons with an average molecular weight of 200 to 3.
The reason why the average carbon number is 15 to 25 is that if the lubricant is less than that, the lubricant will run off when heated immediately before the molding press, and if it is more than that, the fluidity after heating will be lacking.

潤滑剤の塗布量を1〜8 ”/ / dtl としたの
は1グ/dゴ以下では塗布の効果がなく、8ツ/dゴを
越えると巻き取り時に巻きズレが発生したりして好まし
く力い。
It is preferable to apply the lubricant in an amount of 1 to 8 inches per dtl because if it is less than 1 g/dtl, the coating will not be effective, and if it exceeds 8 g/dtl, the winding may become misaligned during winding. Powerful.

成形プレス直前における熱風加熱の温度はアルミ板体の
表面温度50℃以下では加熱の効果が少なく200℃を
越えて加熱しても潤滑剤の変質が起きたり流動性が大き
くカリ過ぎて好ましく力い。
The temperature of hot air heating immediately before the forming press is not desirable because if the surface temperature of the aluminum plate is below 50°C, the heating effect will be small, and if it is heated above 200°C, the lubricant will change in quality or the fluidity will be too strong. .

芹適範囲は処理板表面温度で50℃〜200℃である。The suitable range is 50°C to 200°C in terms of the surface temperature of the treated plate.

以下本発明の具体的実施例について述べる。Specific examples of the present invention will be described below.

実施例工。Example work.

JIS1200−H26アルミニウム板(厚さ0.11
1 ’5朋、rl] 1000 tnwt、長さ600
0m)’(mトリエタノールアミン水溶液(トリエタノ
ール濃度3000ppm、 PH10)中に約95℃で
3分間浸漬処理し、皮膜厚* 10 my/’drrt
 とし、その後シャワー水洗して約150℃で15秒間
乾燥した。
JIS1200-H26 aluminum plate (thickness 0.11
1 '5, RL] 1000 tnwt, length 600
0m)'(mImmersion treatment in triethanolamine aqueous solution (triethanol concentration 3000ppm, PH10) at approximately 95°C for 3 minutes to reduce film thickness* 10 my/'drrt
After that, it was washed with shower water and dried at about 150° C. for 15 seconds.

水利酸化皮膜の形成されたアルミニウム・級を乾燥した
後プレス油〔シェル石油化学■提供品:パラフィンを主
体とする平均分子量270〜300、平均炭素数(n)
19〜22、動粘度6〜9 cst (40℃)〕を約
5 mg / di塗布後巻き取った。その後ドローレ
スプレス機の成形プレス直前において70℃の雰囲気で
加熱した後、所定の形状に打抜くと共に成形してフィン
を得た。この製品はフレア一部の飛びや割れない良好な
ものであった。
After drying the aluminum grade on which the water conservation oxidation film has been formed, press oil [Shell Petrochemical] Provided by: Paraffin-based average molecular weight 270-300, average carbon number (n)
19-22, kinematic viscosity 6-9 cst (40°C)] at about 5 mg/di and then wound up. Thereafter, it was heated in an atmosphere of 70° C. immediately before the forming press of a drawless press, and then punched and molded into a predetermined shape to obtain fins. This product was in good condition with no part of the flare flying off or cracking.

実施例2゜ 実施例1.と同種のアルミニウム板の表面をアロジンI
’tkx t 200にて処理してクロメート皮膜3m
q/dm+形成して、150°05秒間乾燥した。
Example 2゜Example 1. The surface of an aluminum plate of the same type as Alodine I
Chromate film 3m after treatment with 'tkxt 200
q/dm+ was formed and dried for 150°05 seconds.

該アルミニウム板1ρ表面にプレス油(シェル石油■提
供品)を1 m9 / dm”塗布して巻き取った。
1 m9/dm of press oil (supplied by Shell Oil) was applied to the surface of the aluminum plate 1ρ, and the plate was rolled up.

該アルミニウム板を成形プレス直前に於いて70℃の雰
囲気で数秒間加熱し、ドローレスプレス加工後所定のフ
ィンを得た。このフィンはフレア一部の飛びや割れのな
い良好なものであった。
The aluminum plate was heated in an atmosphere of 70° C. for several seconds immediately before forming and pressing, and a predetermined fin was obtained after drawless pressing. This fin was in good condition with no part of the flare flying or cracking.

実施例:3 JI81.2QQH,267ルミニウム板体表面厚さ0
.115叩、巾1000mm、長さ:6000m)?:
エッチングによる脱脂後肢表面K、例えば、ASM41
55改(関西ペイント社:水分散型シリカーアクリル複
合体−メラミン樹脂型塗料)をリバースロール方式で塗
布し、塗布後200〜220℃のメタル温度で20秒間
乾燥して巻き取った。この材料の表面に形成された塗膜
量は15〜/ diであった。
Example: 3 JI81.2QQH, 267 aluminum plate surface thickness 0
.. 115 strokes, width 1000mm, length: 6000m)? :
Degreased hindlimb surface K by etching, e.g. ASM41
55 Kai (Kansai Paint Co., Ltd.: water-dispersed silica-acrylic composite-melamine resin type paint) was applied using a reverse roll method, and after application, it was dried at a metal temperature of 200 to 220°C for 20 seconds and rolled up. The amount of coating formed on the surface of this material was 15~/di.

ざらに該アルミニウム板体にプレス油〔(シェル石油化
学■提供品)平均分子量:200、平均炭素数(n) 
: 15、動粘度:5cst(40℃)含有水分量:1
00111m以下〕を約3 m9/ dm7塗布して巻
取った。該板体を成形プレス直前において150℃の雰
囲気に5秒間保持後ドローレスプレス機により所定形状
のフィンを得た。このフィンは良好な形状を保ちフレア
一部の破損等も発生しなかっ九実施例:4 、T 18120+0+H26アルミニウム板(Hサ0
. l 4 i5mtx、 I 1000 rr、*、
長さ:6000m)の表面を次亜ハロゲン酸塩水溶液(
次亜ハロゲン酸イオン濃度:1000回、PH10,5
)中C(,95℃で3分間浸漬して約12〜/dn−の
酸化皮膜を得た。
Pressing oil [(provided by Shell Petrochemical ■) average molecular weight: 200, average carbon number (n) was applied to the aluminum plate.
: 15, Kinematic viscosity: 5cst (40℃) Moisture content: 1
00111 m or less] was applied in an amount of about 3 m9/dm7 and wound up. The plate was held in an atmosphere at 150° C. for 5 seconds immediately before a forming press, and then a fin of a predetermined shape was obtained using a drawless press. This fin maintained a good shape and did not cause any damage to part of the flare.9 Example: 4, T18120+0+H26 aluminum plate (H
.. l 4 i5mtx, I 1000 rr, *,
The surface of the length: 6000 m) was coated with an aqueous hypohalite solution (
Hypohalite ion concentration: 1000 times, PH10.5
) in C (, 95°C for 3 minutes to obtain an oxide film of about 12~/dn-).

該アルミニウム板体表面を93℃の水ガラス水溶液(1
号水ガラス、濃度5 o 9 /iJ、PH12,4)
で30秒間処理後乾燥した。ついで該アルミニウム板体
表面にプレス油(シェル石油化学■)提供品)5 mq
 / dy+“を塗布した。その後で成形プレス1α前
に於いて該アルミ土つム板・を120”O,に−加熱後
、ドローレスプレス機により所定の形状フィンを得た。
The surface of the aluminum plate was soaked in a 93°C water glass aqueous solution (1
No.3 water glass, concentration 5 o 9 /iJ, PH12,4)
After treatment for 30 seconds, it was dried. Next, press oil (supplied by Shell Petrochemical ■) 5 mq was applied to the surface of the aluminum plate.
After that, the aluminum clay shingle plate was heated to 120" O in front of a forming press 1α, and a fin of a predetermined shape was obtained using a drawless press.

このフィンは、フレア一部の破損のない良好な形状を有
するものであった。
This fin had a good shape with no damage to the flare part.

比較例−1 実施例−1と同様に表面処理して酸化皮膜金膜けた後潤
滑剤塗布及びJJn熱なしに該アルミニウム板をドロー
レスプレスによりフィンに加工したがフレア一部に破損
が出て良好な製品とはならなかった。
Comparative Example-1 The aluminum plate was processed into a fin by a drawless press without applying lubricant or JJN heat after surface treatment to remove the oxide film and gold film in the same manner as in Example-1, but the flare was partially damaged but was not good. It was not a good product.

比較例−2 実施例1と同様に表面処理して酸化皮膜を設けた後潤滑
剤を塗布した。ついで加熱なしに通常の加工法圧てフィ
ンを加工したがフレア一部に割れが発生して良好な製品
とならなかった。
Comparative Example 2 After surface treatment was performed to form an oxide film in the same manner as in Example 1, a lubricant was applied. Next, a pressure fin was processed using the normal processing method without heating, but cracks occurred in a portion of the flare and the product was not good.

上記するような方法により熱交換器用のフィンを形成す
ると加工時にフレア一部に飛びゃ割れの発生がないので
加工歩留りをJげるばがりでなく、成型が確実なので精
度の高い−、フィンを作ることが出来るので熱交換体を
組み立てると熱交換効率等もバラツキのない品質の高い
熱交換器を得ることが出来るようになった。
When fins for heat exchangers are formed using the method described above, there will be no cracking in the flare part during processing, so the processing yield will not only increase, but the molding will be reliable, resulting in high precision fins. By assembling the heat exchanger, it is now possible to obtain a high quality heat exchanger with consistent heat exchange efficiency.

Claims (1)

【特許請求の範囲】 1)アルミニウムまたはアルミニウム合金展伸材の表面
に有機皮膜もしくは無機皮膜を形成し、該展伸材をプレ
ス加工するととKより熱交換用フィンを製造する工程に
於いて、該展伸材を製造工程の巻き取り前に於いて、パ
ラフィン系及びナフテン系の炭化水素を基材とする潤滑
材を塗布する工程と、この潤滑剤が塗布2)潤滑剤の組
成が平均炭素数軸)が15〜25であり平均分子量が2
00〜350よりなるパラフィン系炭化水素(CnHz
n+2)及び、ナフテン系炭化水素(CnHgn )よ
シなる混合物を主成分とすることを特徴とする特許請求
の範囲第1項記軟の熱交要器用フィンの製造法。 3)塗布量が1〜8m!/ / d%’で、水分濃度が
1501f以下、粘度が5〜10c’5tVc調整され
た潤滑材全使用すること全特徴とする特許請求の範囲第
1項及び第2項記載の熱交換器フィンの製造法。 4)成形プレス直前に於いてフィン材料の界面温度が5
0″〜7200℃に加熱して活性化することを特徴とす
る特許請求の範囲第1項〜第3項記載の熱交換器用フィ
ンの製造法。
[Claims] 1) In the process of forming an organic film or an inorganic film on the surface of a wrought aluminum or aluminum alloy material and press-working the wrought material, a heat exchange fin is produced from K. Before winding up the wrought material in the manufacturing process, there is a step of applying a lubricant based on paraffinic and naphthenic hydrocarbons; number axis) is 15 to 25 and the average molecular weight is 2
Paraffinic hydrocarbons consisting of 00 to 350 (CnHz
2. The method for producing a soft heat exchanger fin as set forth in claim 1, characterized in that the main component is a mixture of Cn+2) and naphthenic hydrocarbon (CnHgn). 3) Coating amount is 1-8m! The heat exchanger fin according to claims 1 and 2, characterized in that a lubricant having a water concentration of 1501 f or less and a viscosity of 5 to 10 c'5tVc is used. manufacturing method. 4) Immediately before the forming press, the interface temperature of the fin material is 5.
A method for manufacturing a heat exchanger fin according to claims 1 to 3, wherein the fin is activated by heating to 0'' to 7200°C.
JP58245095A 1983-12-28 1983-12-28 Production of fin for heat exchanger Granted JPS60141337A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58245095A JPS60141337A (en) 1983-12-28 1983-12-28 Production of fin for heat exchanger

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58245095A JPS60141337A (en) 1983-12-28 1983-12-28 Production of fin for heat exchanger

Publications (2)

Publication Number Publication Date
JPS60141337A true JPS60141337A (en) 1985-07-26
JPH024379B2 JPH024379B2 (en) 1990-01-29

Family

ID=17128528

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58245095A Granted JPS60141337A (en) 1983-12-28 1983-12-28 Production of fin for heat exchanger

Country Status (1)

Country Link
JP (1) JPS60141337A (en)

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS545847A (en) * 1977-06-16 1979-01-17 Nippon Packaging Kk Lubricant for cold processing of metal
JPS5418462A (en) * 1977-07-11 1979-02-10 Nippon Paint Co Ltd Surface treating agent for plastic work of metal
JPS558440A (en) * 1978-07-04 1980-01-22 Nippon Steel Corp Production of surface treated steel plate
JPS55149727A (en) * 1979-05-11 1980-11-21 Furukawa Alum Co Ltd Press forming method for sheet of aluminum or aluminum-alloy

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS545847A (en) * 1977-06-16 1979-01-17 Nippon Packaging Kk Lubricant for cold processing of metal
JPS5418462A (en) * 1977-07-11 1979-02-10 Nippon Paint Co Ltd Surface treating agent for plastic work of metal
JPS558440A (en) * 1978-07-04 1980-01-22 Nippon Steel Corp Production of surface treated steel plate
JPS55149727A (en) * 1979-05-11 1980-11-21 Furukawa Alum Co Ltd Press forming method for sheet of aluminum or aluminum-alloy

Also Published As

Publication number Publication date
JPH024379B2 (en) 1990-01-29

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