JPH024379B2 - - Google Patents
Info
- Publication number
- JPH024379B2 JPH024379B2 JP58245095A JP24509583A JPH024379B2 JP H024379 B2 JPH024379 B2 JP H024379B2 JP 58245095 A JP58245095 A JP 58245095A JP 24509583 A JP24509583 A JP 24509583A JP H024379 B2 JPH024379 B2 JP H024379B2
- Authority
- JP
- Japan
- Prior art keywords
- heat exchanger
- lubricant
- aluminum plate
- manufacturing
- exchanger fin
- 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
- 229910052782 aluminium Inorganic materials 0.000 claims description 22
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 22
- 239000000314 lubricant Substances 0.000 claims description 13
- 150000002430 hydrocarbons Chemical class 0.000 claims description 10
- 229930195733 hydrocarbon Natural products 0.000 claims description 9
- 238000004519 manufacturing process Methods 0.000 claims description 9
- 238000010438 heat treatment Methods 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 6
- 238000004381 surface treatment Methods 0.000 claims description 5
- 239000000463 material Substances 0.000 claims description 4
- 239000000203 mixture Substances 0.000 claims description 4
- 238000004804 winding Methods 0.000 claims description 4
- 238000003825 pressing Methods 0.000 claims description 2
- 239000004215 Carbon black (E152) Substances 0.000 claims 2
- 229910000838 Al alloy Inorganic materials 0.000 claims 1
- 239000000956 alloy Substances 0.000 claims 1
- 238000005336 cracking Methods 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 230000007797 corrosion Effects 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 2
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical compound [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 229920000620 organic polymer Polymers 0.000 description 2
- 235000019353 potassium silicate Nutrition 0.000 description 2
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 229910001593 boehmite Inorganic materials 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- FAHBNUUHRFUEAI-UHFFFAOYSA-M hydroxidooxidoaluminium Chemical compound O[Al]=O FAHBNUUHRFUEAI-UHFFFAOYSA-M 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M101/00—Lubricating compositions characterised by the base-material being a mineral or fatty oil
- C10M101/02—Petroleum fractions
-
- C—CHEMISTRY; METALLURGY
- C23—COATING 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
- C23C—COATING 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
- C23C24/00—Coating starting from inorganic powder
- C23C24/08—Coating starting from inorganic powder by application of heat or pressure and heat
-
- C—CHEMISTRY; METALLURGY
- C23—COATING 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
- C23C—COATING 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
- C23C28/00—Coating 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)
Description
【発明の詳細な説明】
［産業上の利用分野］
本発明は家庭用冷熱機器や自動車等の熱交換機
器に使用される熱交換器用フインの製造方法に係
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アルミニウム板をドロ
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イン
の製造法に関するものである。[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to a method for manufacturing heat exchanger fins used in heat exchange equipment for household cooling and heating equipment, automobiles, etc. (Hereinafter simply referred to as an aluminum plate) When applying an inorganic or organic film or a composite film of these on the surface of the aluminum plate, the aluminum plate has good formability and corrosion resistance. The present invention relates to a method for manufacturing heat exchanger fins with excellent heat exchange efficiency.
［従来技術とその問題点］
従来アルミニウム板は上記したごとく表面処理
を施した後、例えばドローレスプレス加工をして
熱交換器用フインを製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
と称する事故が起こり、しばしば熱交換器用部材
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
場合があつた。[Prior art and its problems] Conventionally, when an aluminum plate is subjected to surface treatment as described above and then subjected to drawless press processing to produce heat exchanger fins, flare flying or flare cracking occurs during press processing. Accidents such as this often occur, and the performance as a heat exchanger member such as corrosion resistance and heat exchange rate deteriorates, and in extreme cases, it may become unusable.
［発明の開示］
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
の質、量及び付着状態が、熱交換器用フイン等の
製造歩留りに大きな影響を持ちうることを見出だ
した。さらに研究の結果、本発明に到達してもの
でありその要旨とするところは、例えば、ベーマ
イト皮膜、クロメート皮膜、陽極酸化皮膜、その
他の手段によつ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アルミニウム
板表面上に、表面処理製造工程の巻き取り前に於
いて脂肪族炭化水素中パラフイン系炭化水素
（CnH2n＋２）、ナフテン系炭化水素（CnH2n）
を１〜８mg／ｄm2付着させて置き、プレス成形直
前に於いて熱風、スチーム加熱等によつて該アル
ミニウム板の表面温度を50〜200℃に加熱するこ
とにより、塗布されているパラフイン系及びナフ
テン系炭化水素を活性化する。この状態で、プレ
ス作業を行うとアルミニウム板等の表面が活性化
されているのでフレアー飛び、フレアー割れ等事
故のない良好なフインを得ることができる。[Disclosure of the Invention] At the stage of various studies regarding the above-mentioned defects, the present inventors discovered that the quality, quantity, and state of adhesion of hydrocarbon compounds adhering to the surface of an aluminum plate can have a great influence on the manufacturing yield of heat exchanger fins, etc. I discovered something. As a result of further research, we have arrived at the present invention, and its gist is, for example, a boehmite film, a chromate film, an anodized film, an inorganic film chemically converted by other means, an organic polymer, or On the surface of an aluminum plate on which a protective film is formed by applying an inorganic-organic polymer, etc., paraffinic hydrocarbons (CnH 2 n+2) in aliphatic hydrocarbons are applied before winding in the surface treatment manufacturing process. Naphthenic hydrocarbons ( CnH2n )
The applied paraffin- based and Activates naphthenic hydrocarbons. When press work is performed in this state, the surface of the aluminum plate etc. is activated, so a good fin can be obtained without any accidents such as flare flying or flare cracking.
本発明に使用される潤滑剤の組成は、パラフイ
ン系炭化水素及びナフテン系炭化水素を主成分と
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、30：70でもまたはこの逆
でもよいものである。また、平均分子量は200〜
350であり、平均炭素数（ｎ）が15〜25の範囲の
ものがよい。尚、粘度は使用条件により異なる
が、40℃に於ける通常の使用状態の粘度は、５〜
10cstの範囲のものが使われる。また、本潤滑剤
中には耐摩性添加物が５％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150ppm以下に押さえた方がよい。以
下本発明の限定理由につき記述する。 The composition of the lubricant used in the present invention is a composition containing paraffinic hydrocarbons and naphthenic hydrocarbons as main components. That is, the ratio of these main components may be, for example, 50:50, 30:70, or vice versa. Also, the average molecular weight is 200~
350, and preferably has an average carbon number (n) in the range of 15 to 25. Although the viscosity varies depending on the usage conditions, the viscosity under normal usage conditions at 40℃ is 5 to 5.
Those in the 10cst range are used. Further, the lubricant may contain 5% or less of a wear-resistant additive, and the water content is preferably kept to 150 ppm or less from the viewpoint of storage stability and corrosion resistance of the treated plate. 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主成分を、パ
ラフイン系及びナフテン系の炭化水素で平均分子
量を200〜350とし、平均炭素数が15〜25としたの
は、それ以下ではプレス成形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 350 and an average carbon number of 15 to 25. This is because when the lubricant is heated, the lubricant flows down, and if the lubricant is heated further than that, it lacks fluidity after heating.
潤滑剤の塗布量を１〜８mg／ｄm2としたのは１
mg／ｄm2以下では塗布の効果がなく、８mg／ｄm2
を超えると巻き取り時に巻きズレが発生したりし
て好ましくない。 The amount of lubricant applied was 1 to 8 mg/ dm2 .
There is no effect of application below mg/dm 2 , and 8 mg/dm 2
Exceeding this is not preferable because winding misalignment may occur during winding.
プレス成形直前に於ける熱風加熱の温度はアル
ミニウム板の表面温度50℃以下では加熱の効果が
少なく、200℃を超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なり過ぎて好ましくな
い。最適範囲は、処理板表面温度で50℃〜200℃
である。 The temperature of hot air heating immediately before press forming is not recommended because if the surface temperature of the aluminum plate is below 50℃, the heating effect will be small, and if it is heated above 200℃, the lubricant will change in quality or the fluidity will become too large. do not have. The optimum range is 50℃ to 200℃ for the surface temperature of the treated plate.
It is.
以下、本発明の具体的実施例について述べる。 Hereinafter, specific examples of the present invention will be described.
［実施例］
実施例 １
JIS1200−H26 アルミニウム板（厚さ：0.115
mm、巾：1000mm、長さ：6000mm）をトリエタノー
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、皮膜厚を10mg／ｄm2とし、その後シヤワー水
洗して約150℃で15秒間乾燥した。[Example] Example 1 JIS1200-H26 aluminum plate (thickness: 0.115
mm, width: 1000mm, length: 6000mm) with a triethanolamine aqueous solution (triethanol concentration:
3000 ppm, pH 10) for 3 minutes at about 95°C to give a film thickness of 10 mg/dm 2 , followed by washing with shower water and drying at about 150°C for 15 seconds.
水和酸化皮膜の形成されたアルミニウム板を乾
燥した後プレス油〔シエル石油化学(株)提供品パラ
フイ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：６〜9cst（40℃）〕
を約５mg／ｄm2塗布後巻き取つた。その後ドロー
レスプレス機のプレス成形直前において70℃の雰
囲気で加熱した後、所定の形状に打ち抜くと共に
成形してフインを得た。この製品はフレアー部の
飛びや割れない良好なものであつた。 After drying the aluminum plate on which the hydrated oxide film has been formed, press oil (provided by Ciel Petrochemical Co., Ltd.) Mainly contains paraffin Average molecular weight: 270-300, Average number of carbons (n): 19-22, Kinematic viscosity :6~9cst (40℃)]
After applying about 5 mg/dm 2 of the material, it was rolled up. Thereafter, it was heated in an atmosphere of 70°C immediately before press forming using a drawless press machine, and then punched and molded into a predetermined shape to obtain fins. This product was in good condition with no flared parts or cracks.
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No.1200にて処理してクロメート皮膜３mg／ｄ
m2を形成して、150℃で５秒間乾燥した。該アル
ミニウム板の表面にプレス油〔シエル石油(株)提供
品〕を１mg／ｄm2塗布して巻き取つた。Example 2 The surface of the same type of aluminum plate as in Example 1 was treated with Alodine No. 1200 to form a chromate film of 3 mg/d.
m 2 was formed and dried at 150° C. for 5 seconds. The surface of the aluminum plate was coated with 1 mg/dm 2 of press oil (supplied by Shell Oil Co., Ltd.) and wound up.
該アルミニウム板をプレス成形直前に於いて70
℃の雰囲気で数秒間加熱し、ドローレスプレス加
工後所定のフインを得た。このフインは、フレア
ー部の飛びや割れのない良好なものであつた。 Immediately before press forming the aluminum plate, 70
It was heated for several seconds in an atmosphere of .degree. C., and after drawless pressing, a predetermined fin was obtained. This fin was in good condition with no flying or cracking in the flare portion.
実施例 ３
JIS1200−H26アルミニウム板（表面厚さ：
0.115mm、巾：1000mm、長さ：6000ｍ）をエツチ
ングによる脱脂後該表面に、例えば、ASM4155
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つた。この材料の表面に形
成された塗膜量は15mg／ｄm2であつた。さらに、
該アルミニウム板にプレス油〔シエル石油(株)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：100ppm以下〕
を約３mg／ｄm2塗布して巻き取つた。該アルミニ
ウム板をプレス成形直前に於いて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
形状のフインを得た。このフインは良好な形状を
保をフレアー部の破損等も発生しなかつた。Example 3 JIS1200-H26 aluminum plate (surface thickness:
0.115mm, Width: 1000mm, Length: 6000m).
Kai (Kansai Paint Co., Ltd.: water-dispersed silica-acrylic composite-melamine resin type paint) is applied using a reverse roll method, and after application, the metal temperature is 200 to 220℃.
It was dried for 20 seconds and rolled up. The amount of coating formed on the surface of this material was 15 mg/dm 2 . moreover,
Press oil [provided by Ciel Sekiyu Co., Ltd., average molecular weight: 200, average carbon number (n): 15, kinematic viscosity: 5 cst (40°C), water content: 100 ppm or less] is applied to the aluminum plate.
Approximately 3 mg/dm 2 of the material was applied and wound. The aluminum plate was held in an atmosphere at 150° C. for 5 seconds immediately before press forming, and then a fin of a predetermined shape was obtained using a drawless press. This fin maintained a good shape and no damage to the flared portion occurred.
実施例 ４
JIS1200−H26アルミニウム板（厚さ：0.115
mm、巾：1000mm、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：
1000ppm、PH10.5）中に、95℃で３分間浸漬して
約12mg／ｄm2の酸化皮膜を得た。該アルミニウム
板表面を93℃の水ガラス水溶液（１号水ガラス、
濃度：50ｇ／ｌ、PH12.4）で30秒間処理後乾燥し
た。ついで、該アルミニウム板表面にプレス油
〔シエル石油(株)提供品〕５mg／ｄm2を塗布した。
さらに、プレス成形直前に於いて該アルミニウム
板を120℃に加熱後、ドローレスプレス機により
所定形状のフインを得た。このフインは、フレア
ー部の破損のない良好な形状を有するものであつ
た。Example 4 JIS1200-H26 aluminum plate (thickness: 0.115
mm, width: 1000mm, length: 6000m) with a hypohalite aqueous solution (hypohalite ion concentration:
1000 ppm, pH 10.5) for 3 minutes at 95°C to obtain an oxide film of approximately 12 mg/dm 2 . The surface of the aluminum plate was soaked in a 93°C water glass solution (No. 1 water glass,
Concentration: 50 g/l, pH 12.4) for 30 seconds and then dried. Then, 5 mg/dm 2 of press oil (supplied by Shell Oil Co., Ltd.) was applied to the surface of the aluminum plate.
Furthermore, immediately before press forming, the aluminum plate was heated to 120°C, and then a fin of a predetermined shape was obtained using a drawless press. This fin had a good shape with no damage to the flared portion.
比較例 １
実施例１と同様に表面処理して酸化皮膜を設け
た後、潤滑剤塗布及び加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インに加工した
が、このフインはフレアー部に破損が出て良好な
製品とならなかつた。Comparative Example 1 After surface treatment to form an oxide film in the same manner as in Example 1, the aluminum plate was processed into fins using a drawless press without applying lubricant or heating, but the fins were damaged at the flared part. 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
常の加工法にてフインを加工したが、このフイン
は、フレアー部に割れが発生して良好な製品とな
らなかつた。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, the fins were processed using a normal processing method without heating, but cracks occurred in the flared portions of the fins and the product was not a good product.
［発明の効果］
上記するような方法により熱交換器フインを形
成すると、加工時にフレアー部に飛びや割れの発
生がないので加工歩留りを上げるばかりでなく、
成型が確実なので精度の高い、フインを作ること
が出来、熱交換体を組み立てると熱交換率等もバ
ラツキのない品質の高い熱交換器を得ることが出
来るようになつた。[Effects of the Invention] When heat exchanger fins are formed by the method described above, there is no occurrence of flying or cracking in the flare portion during processing, which not only increases the processing yield, but also increases the processing yield.
Since the molding is reliable, it is possible to make highly accurate fins, and when the heat exchanger is assembled, it is now possible to obtain a high quality heat exchanger with consistent heat exchange efficiency.
Claims (1)
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ことにより熱交換器用フイ
ンを製造する工程において、該展伸材の表面処理
製造工程の巻き取り前において、パラフイン系お
よびナフテン系の炭化水素を基材とする潤滑剤を
塗布する工程と、この潤滑剤が塗布された展伸材
を、プレス成形直前において成形材の表面温度が
50〜200℃に加熱してからプレス成形する工程と
からなることを特徴とする熱交換器用フインの製
造法。 ２ 潤滑剤の組成が平均炭素数（ｎ）が15〜25で
あり、平均分子量が200〜350よりなるパラフイン
系炭化水素（CoH2o+2）および、ナフテン系炭化
水素（CoH2o）よりなる混合物を主成分とする特
許請求の範囲第１項記載の熱交換器用フインの製
造法。 ３ 塗布量が１〜８mg／ｄm2で、水分含有量が
150ppm以下であり、プレス加工時の粘度が５〜
10cstに調整された潤滑剤を使用することを特徴
とする特許請求の範囲第１項または、第２項記載
の熱交換器用フインの製造法。[Scope of Claims] 1. In the step of manufacturing a heat exchanger fin by forming an organic film or an inorganic film on the surface of a wrought aluminum or aluminum alloy material and pressing the wrought material, Before winding in the surface treatment manufacturing process, a lubricant based on paraffinic and naphthenic hydrocarbons is applied. surface temperature
A method for manufacturing heat exchanger fins, comprising the steps of heating to 50 to 200°C and then press forming. 2 The composition of the lubricant is paraffinic hydrocarbon (C o H 2o+2 ) and naphthenic hydrocarbon (C o H 2o ) A method for producing a heat exchanger fin according to claim 1, the main component of which is a mixture consisting of: 3 Application amount is 1 to 8mg/ dm2 and moisture content is
150ppm or less, and the viscosity during press processing is 5~5
A method for manufacturing a heat exchanger fin according to claim 1 or 2, characterized in that a lubricant adjusted to 10cst is used.
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 JPS60141337A (en) | 1985-07-26 |
| JPH024379B2 true 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)
| 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 |
-
1983
- 1983-12-28 JP JP58245095A patent/JPS60141337A/en active Granted
Patent Citations (4)
| 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 |
|---|---|
| JPS60141337A (en) | 1985-07-26 |
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