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JPH0156146B2 - - Google Patents
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JPH0156146B2 - - Google Patents

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Publication number
JPH0156146B2
JPH0156146B2 JP20488982A JP20488982A JPH0156146B2 JP H0156146 B2 JPH0156146 B2 JP H0156146B2 JP 20488982 A JP20488982 A JP 20488982A JP 20488982 A JP20488982 A JP 20488982A JP H0156146 B2 JPH0156146 B2 JP H0156146B2
Authority
JP
Japan
Prior art keywords
thin plate
solution
alloy thin
less
surface area
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
Application number
JP20488982A
Other languages
Japanese (ja)
Other versions
JPS5996274A (en
Inventor
Ken Toma
Isao Takeuchi
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 JP20488982A priority Critical patent/JPS5996274A/en
Publication of JPS5996274A publication Critical patent/JPS5996274A/en
Publication of JPH0156146B2 publication Critical patent/JPH0156146B2/ja
Granted legal-status Critical Current

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  • ing And Chemical Polishing (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

この発明は、Al合金薄板の表面積を拡大する
方法、特に熱交換器用Al合金製フイン材にすぐ
れた防食性と水切り性を付与するために、その表
面積を拡大する方法に関する。 一般に、Al合金は熱伝導性、塑性(圧延)加
工性、成形加工性および耐食性にすぐれているの
で、これらの特性が要求される熱交換器のフイン
材の製造に広く利用されており、熱媒体を通す管
材と、主として熱交換の役割を果すフイン材とを
含む熱交換器では特に管材の耐食性が重視される
ところから、フイン材を管材よりも電気化学的に
卑な材料で構成し、そのフイン材のいわゆる犠牲
陽極効果によつて管材を防食することが広く行わ
れている。このような犠牲陽極効果の大小は、防
食する側のフイン材と防食される側の管材との、
水と接触する表面の面積比によつて左右され、こ
の比が大きいほど、すなわちフイン材の表面積が
大きいほどその効果が顕著に発揮できるので、フ
イン材の表面積を拡大する方法が従来望まれてい
た。 また、Al合金製フイン材の表面は水切り性に
劣るために、熱交換器使用時にフイン材表面に付
着した結露水は水滴となり、さらに成長して隣り
のフイン部材にまで達し、フイン部材相互間の空
間を広い範囲に亘つて水滴が完全に埋めつくして
しまうことから、大気中の熱交換媒体の役割を果
している空気の流通が悪化すると共にその水が熱
の伝達を妨害し、熱交換性能は著しく低下するも
のとなる。このようにAl合金製フイン材の水切
り性が劣るのは、冷間圧延後のAl合金薄板の表
面がきわめて平滑な光沢面となつていることに起
因し、このような表面上に擬縮した水はその大き
な表面張力によつて大きな水滴を形成するように
なるのであり、したがつて、付着した結露水が大
きな水滴となる前に容易に流失してしまう表面、
すなわち、すぐれた水切れ性の表面を有するフイ
ン材が望まれていた。 そこで、以上のような防食性と水切れ性にすぐ
れているという特性は、凹凸に富んで表面積が拡
大した表面をフイン材に形成させることによつて
得られるが、酸またはアルカリ溶液中に単に浸漬
するだけの化学エツチングでは、多少の凹凸が得
られても微視的に細かい凹凸表面は得られず、一
方電解法(電解エツチング)では、特別に電解設
備を必要とし、複雑微妙な電解条件を設定しなけ
ればならない上に、処理時間が著しく長くなり、
実用上コスト、操業両面に難点があつた。 本発明者等は、上述のような観点から、電解法
によることなく、化学エツチングによつてAl合
金薄板表面に微細な凹凸を形成させるべく種々研
究を行なつた結果、少なくともSn:0.05〜0.3重
量%を含有したAl合金薄板に、500〜630℃の範
囲内の温度で溶体化処理を施した後、PH:3.5以
下の酸性水溶液中で1〜60分浸漬の化学エツチン
グを施してAl合金薄板全表面に微細な凹凸を形
成させ、その後中和水洗処理を施してエツチング
液を除去すると、Al合金薄板表面には微細な凹
凸が生じてその表面積は著しく拡大し、この結果
のAl合金薄板をフイン材として使用した場合、
すぐれた防食性と水切り性を発揮するようになる
という知見を得たのである。 したがつて、この発明は、上記知見にもとづい
てなされたものであつて、少なくともSn:0.05〜
0.3重量%を含有するAl合金薄板を、500〜630℃
の範囲内の温度で溶体化処理した後、PH:3.5以
下の酸性水溶液中に1〜60分間浸漬の条件で化学
エツチングを施し、その後中和水洗処理を施すこ
とを特徴とする、Al合金薄板の表面積拡大方法
を提供するものである。 この発明においてエツチング液として使用され
る上記の酸性水溶液は、種々の金属の塩化物水溶
液、例えば塩化アルミニウム水溶液が好ましい
が、従来この分野において使用されているその他
の酸性水溶液、例えば硫酸アルミニウム水溶液を
使用することもできる。 つぎに、この発明において、Al合金薄板のSn
含有量、溶体化処理温度およびエツチング条件を
上記のとおりに限定した理由を述べる。 (a) Al合金薄板のSn含有量 通常のAl合金薄板は、その表面に自然に形
成された比較的強固な酸化皮膜によつて覆われ
ているために、中性水溶液中では極めて緩慢に
溶解するにすぎず、また酸性水溶液中では溶解
速度は増大するものの、全面が均一に溶解する
状態で溶解が進行するので、化学エツチング後
の表面は比較的滑らかになる。これに対して、
Al合金薄板にSnを合金成分として固溶含有さ
せると表面の酸化皮膜は弱まつて、中性水溶液
中でも緩慢に溶解するようになるが、酸性水溶
液中ではさらに溶解速度が増大して速かに溶解
すると共に、溶解は滑らかに行なわれず、薄板
表面に微細な凹凸を形成しつつ進行するので、
表面積は著しく拡大されるようになる。しかし
薄板中のSn含有量が0.05重量%未満であると、
適切な溶体化処理を行なつても上記効果が得ら
れず、一方0.3重量%を越えて含有させても前
記作用により一層の向上効果はみられないとこ
ろから、Snの含有量を0.05〜0.3重量%と定め
た。 (b) 溶体化処理温度 (a)で述べた効果は、Al合金薄板にSnを含有
させるだけでなく、さらにSn含有Al合金薄板
に溶体化処理を施して初めて得られる。一般
に、Al合金中へのSnの固溶度は高々0.1重量%
で極めて小さく、室温では殆ど固溶化されな
い。Al合金中へのSnの固溶度は500℃以上で大
きくなり、600℃附近で最大となるから、500℃
未満では溶体化効果が十分発揮されず、一方
630℃を越えた溶体化処理では効果の向上がみ
られないばかりか軟化が著しく、薄板によつて
は一部溶解する危険性もあることから、溶体化
処理温度を500〜630℃と定めた。 (c) 化学エツチング条件 (a)で述べたように、Snを固溶したAl合金薄
板は酸性水溶液中でのみ速かに溶解して微細な
凹凸を形成するが、溶液のPHが3.5を越えると
溶解の進行が緩慢になると共に、明瞭な凹凸が
形成されないので、エツチング液のPHを3.5以
下と定めた。またエツチング時間が1分間未満
では十分な凹凸が形成されるほど溶解が進ま
ず、また60分間を越えて浸漬すると、表面積増
大効果によつて溶解速度が急激に増大して溶解
による損失が増大するところから、浸漬時間を
1〜60分間と定めた。 つぎに、この発明の方法を実施例によつて具体
的に説明する。 実施例 通常の溶解法により、それぞれ第1表に示され
る最終成分組成をもつた溶湯を調製し、鋳造して
鋳塊とした後、温度:580℃に15時間保持の条件
で均質化処理を施し、ついで面削後、通常の条件
にて熱間圧延、並びに中間焼鈍を間にはさんでの
冷間圧延を行なつて、それぞれ板厚:0.15mmおよ
び0.5mmの薄板とし、これらの薄板に同じく第1
表に示される条件にて溶体化処理(強制空冷)を
施し、これらの溶体化処理後の薄板のうち、板
厚:0.5mmのものには冷間圧延を施して0.15mmの
板厚とし、引続いてこの結果の薄板に対して、化
学エツチング液として、液温:40℃、PH:2.5の
1規定AlCl3水溶液、液温:40℃、PH:3.0の1規
定Al2(SO43水溶液、または液温:40℃、PH:6.0
の1規定NaCl水溶液を使用し、それぞれ第1表
に示される時間浸漬の条件で化学エツチングを施
し、最終的に中和水洗処理を施すことによつて本
発明方法1〜19および比較方法1〜7をそれぞれ
実施した。 なお、比較方法1〜7は、Al合金薄板のSn含
有量、溶体化処理、および化学エツチングのうち
のいずれかの条件(第1表に※印を付す)がこの
発明の範囲から外れた条件で実施したものであ
る。また、上記のAl合金鋳塊は、いずれも第1
表には表示を省略したが、不可避不純物として、
Fe:0.25%以下、Si:0.13%以下、Cu:0.09%以
下、Mn:0.1%以下、Ti:0.1%以下、Cr:0.1%
以下、Mg:0.1%以下、Zr:0.05%以下、および
Zn:0.05%以下を含有するものであつた。 ついで、本発明方法1〜19および比較方法1〜
7によつて処理されたAl合金薄板について、カ
ロメル電極を基準電極とした自然電位
(Ecorr):約−1350mVから100mV貴に定電位
保持したときに得られるアノード電流(正電流)
を測定し、この値を、化学エツチング直前に測定
しておいたアノード電流と比較し、化学エツチン
グ直前のアノード電流値を100とし、これに対す
る増加率により表面積の増加割合を評価した。こ
れらの結果を第1表に合せて示した。 第1表に示される結果から、本発明方法1〜19
によつて処理されたAl合金薄板においては、い
The present invention relates to a method of increasing the surface area of an Al alloy thin plate, and more particularly to a method of increasing the surface area of an Al alloy fin material for a heat exchanger in order to impart excellent corrosion resistance and drainage properties. In general, Al alloys have excellent thermal conductivity, plastic (rolling) workability, moldability, and corrosion resistance, so they are widely used in the production of heat exchanger fin materials that require these properties. In a heat exchanger that includes a tube material through which a medium passes and a fin material that primarily plays the role of heat exchange, corrosion resistance of the tube material is particularly important, so the fin material is made of a material that is less electrochemically base than the tube material. It is widely practiced to prevent corrosion of pipe materials by the so-called sacrificial anode effect of the fin material. The magnitude of this sacrificial anode effect depends on the relationship between the fin material on the corrosion-protecting side and the pipe material on the corrosion-protected side.
It depends on the area ratio of the surface in contact with water, and the larger the ratio, that is, the larger the surface area of the fin material, the more pronounced the effect can be.Therefore, a method of expanding the surface area of the fin material has been desired. Ta. In addition, since the surface of the Al alloy fin material has poor drainage properties, condensed water that adheres to the surface of the fin material when a heat exchanger is used turns into water droplets, grows further, and reaches adjacent fin members, causing gaps between the fin members. As water droplets completely fill a wide area, the circulation of air, which acts as a heat exchange medium in the atmosphere, deteriorates, and the water obstructs heat transfer, reducing heat exchange performance. will decrease significantly. The reason why the Al alloy fin material has poor drainage properties is that the surface of the Al alloy thin plate after cold rolling is an extremely smooth and glossy surface. Water tends to form large droplets due to its large surface tension, and therefore, the surface where the condensed water that adheres to it is easily washed away before it becomes large droplets.
That is, a fin material having a surface with excellent drainage properties has been desired. Therefore, the above-mentioned characteristics of excellent corrosion resistance and water drainage can be obtained by forming a surface of the fin material that is rich in irregularities and has an expanded surface area, but it is possible to obtain the characteristics of excellent corrosion resistance and water drainage by simply immersing it in an acid or alkaline solution. Chemical etching, which only involves etching, does not produce a microscopically fine uneven surface even if some unevenness is obtained.On the other hand, electrolytic methods (electrolytic etching) require special electrolytic equipment and require complex and delicate electrolytic conditions. In addition to having to configure the settings, the processing time is significantly longer.
There were practical difficulties in terms of both cost and operation. From the above-mentioned point of view, the present inventors have conducted various studies to form fine irregularities on the surface of an Al alloy thin plate by chemical etching without using electrolytic methods, and have found that Sn: at least 0.05 to 0.3. After applying solution treatment to an Al alloy thin plate containing % by weight at a temperature within the range of 500 to 630°C, chemical etching was performed by immersion in an acidic aqueous solution with a pH of 3.5 or less for 1 to 60 minutes to form an Al alloy. When fine irregularities are formed on the entire surface of the thin sheet, and then the etching solution is removed by neutralizing water washing, fine irregularities are formed on the surface of the Al alloy thin sheet, and its surface area is significantly expanded. When used as a fin material,
They discovered that it exhibits excellent corrosion resistance and drainage properties. Therefore, this invention has been made based on the above knowledge, and is based on the above-mentioned findings.
Al alloy thin plate containing 0.3% by weight, heated to 500~630℃
An Al alloy thin plate characterized by being subjected to solution treatment at a temperature within the range of , followed by chemical etching under the conditions of immersion in an acidic aqueous solution with a pH of 3.5 or less for 1 to 60 minutes, and then subjected to a neutralizing water washing treatment. The present invention provides a method for enlarging the surface area of. The above acidic aqueous solution used as the etching solution in this invention is preferably an aqueous solution of various metal chlorides, such as an aqueous aluminum chloride solution, but other acidic aqueous solutions conventionally used in this field, such as an aqueous aluminum sulfate solution, may also be used. You can also. Next, in this invention, the Sn of the Al alloy thin plate is
The reason why the content, solution treatment temperature, and etching conditions were limited as described above will be described. (a) Sn content of Al alloy thin plate Ordinary Al alloy thin plate dissolves extremely slowly in a neutral aqueous solution because it is covered with a relatively strong oxide film that is naturally formed on its surface. Although the dissolution rate increases in an acidic aqueous solution, the dissolution proceeds with uniform dissolution over the entire surface, resulting in a relatively smooth surface after chemical etching. On the contrary,
When Sn is incorporated as a solid solution into an Al alloy thin plate, the oxide film on the surface becomes weaker and it dissolves slowly even in a neutral aqueous solution, but the dissolution rate increases even more rapidly in an acidic aqueous solution. As it melts, the melting process does not occur smoothly, but instead forms fine irregularities on the surface of the thin plate.
The surface area becomes significantly enlarged. However, if the Sn content in the thin plate is less than 0.05% by weight,
Even if an appropriate solution treatment is performed, the above effects cannot be obtained, and on the other hand, even if the Sn content exceeds 0.3% by weight, no further improvement effect can be seen due to the above action, so the Sn content is increased from 0.05 to 0.3% by weight. It was determined as weight%. (b) Solution treatment temperature The effect described in (a) can only be obtained not only by incorporating Sn into the Al alloy thin plate but also by subjecting the Sn-containing Al alloy thin plate to solution treatment. Generally, the solid solubility of Sn in Al alloys is at most 0.1% by weight.
It is extremely small and hardly becomes a solid solution at room temperature. The solid solubility of Sn in Al alloy increases above 500℃ and reaches its maximum around 600℃.
If it is less than
Solution treatment at temperatures exceeding 630°C not only does not improve the effect, but also causes significant softening, and there is a risk that some thin plates may melt, so the solution treatment temperature was set at 500 to 630°C. . (c) Chemical etching conditions As mentioned in (a), an Al alloy thin plate containing Sn as a solid solution dissolves quickly and forms fine irregularities only in an acidic aqueous solution, but the pH of the solution exceeds 3.5. The pH of the etching solution was determined to be 3.5 or less because the progress of dissolution becomes slow and clear unevenness is not formed. Furthermore, if the etching time is less than 1 minute, the dissolution will not proceed to the extent that sufficient unevenness is formed, and if the etching time is immersed for more than 60 minutes, the dissolution rate will rapidly increase due to the effect of increasing the surface area, and the loss due to dissolution will increase. Therefore, the immersion time was determined to be 1 to 60 minutes. Next, the method of the present invention will be specifically explained using examples. Example Molten metals having the final component compositions shown in Table 1 were prepared using the usual melting method, cast into ingots, and then homogenized at a temperature of 580°C for 15 hours. After applying and facing, hot rolling under normal conditions and cold rolling with intermediate annealing were performed to obtain thin sheets with thicknesses of 0.15 mm and 0.5 mm, respectively. Similarly, the first
Solution treatment (forced air cooling) was performed under the conditions shown in the table, and among the thin plates after solution treatment, those with a thickness of 0.5 mm were cold rolled to a thickness of 0.15 mm. Subsequently, the resulting thin plate was treated with a 1N AlCl 3 aqueous solution at a temperature of 40°C and a pH of 2.5, and a 1N Al 2 (SO 4 ) solution at a temperature of 40°C and a pH of 3.0 as chemical etching solutions. 3Aqueous solution or liquid temperature: 40℃, PH: 6.0
Methods 1 to 19 of the present invention and comparative methods 1 to 1 were obtained by chemically etching using a 1N NaCl aqueous solution of 7 were carried out respectively. Comparative methods 1 to 7 are conditions in which any one of the Sn content of the Al alloy thin plate, solution treatment, and chemical etching (marked with * in Table 1) is outside the scope of this invention. This was carried out in In addition, all of the above Al alloy ingots are
Although not shown in the table, as an unavoidable impurity,
Fe: 0.25% or less, Si: 0.13% or less, Cu: 0.09% or less, Mn: 0.1% or less, Ti: 0.1% or less, Cr: 0.1%
Below, Mg: 0.1% or less, Zr: 0.05% or less, and
Zn: It contained 0.05% or less. Next, methods 1 to 19 of the present invention and comparative methods 1 to 19
Natural potential (Ecorr) using a calomel electrode as a reference electrode: Anode current (positive current) obtained when the Al alloy thin plate treated by 7 is held at a constant potential from approximately -1350 mV to 100 mV.
was measured, and this value was compared with the anode current measured immediately before chemical etching.The anode current value immediately before chemical etching was set as 100, and the increase rate of the surface area was evaluated based on the increase rate with respect to this value. These results are also shown in Table 1. From the results shown in Table 1, methods 1 to 19 of the present invention
In the Al alloy thin plate treated by

【表】【table】

【表】 れも表面積が著しく増加しているのに対して、比
較方法1〜7によつて処理されたAl合金薄板に
おいては、表面積の著しい増加は期待できないこ
とが明らかである。 上述のように、この発明の方法によれば、Al
合金薄板の表面積を著しく拡大することができ、
したがつてこれを例えば熱交換器のフイン材とし
て使用した場合にはすぐれた防食性(犠牲陽極効
果)および水切り性を発揮し、熱交換器のきわめ
て長期に亘る使用が可能となるなど工業上有用な
効果がもたらされるのである。
[Table] It is clear that while the surface areas of the Al alloy thin sheets treated by Comparative Methods 1 to 7 are significantly increased, no significant increase in surface area can be expected. As mentioned above, according to the method of this invention, Al
The surface area of the alloy thin plate can be significantly expanded,
Therefore, when used as a fin material in a heat exchanger, for example, it exhibits excellent corrosion resistance (sacrificial anode effect) and water removal properties, making it possible to use the heat exchanger for an extremely long period of time. It brings about useful effects.

Claims (1)

【特許請求の範囲】[Claims] 1 少なくともSn:0.05〜0.3重量%を含有する
Al合金薄板を、500〜630℃の範囲内の温度で溶
体化処理した後、PH:3.5以下の酸性水溶液中に
1〜60分間浸漬の条件で化学エツチングを施し、
その後中和水洗処理を施すことを特徴とする、
Al合金薄板の表面積拡大方法。
1 Contains at least Sn: 0.05 to 0.3% by weight
After solution-treating the Al alloy thin plate at a temperature within the range of 500 to 630°C, chemical etching is performed by immersing it in an acidic aqueous solution with a pH of 3.5 or less for 1 to 60 minutes,
It is characterized in that it is then subjected to a neutralizing water washing treatment.
Method for expanding surface area of Al alloy thin plate.
JP20488982A 1982-11-22 1982-11-22 Method for increasing surface area of thin al alloy plate Granted JPS5996274A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP20488982A JPS5996274A (en) 1982-11-22 1982-11-22 Method for increasing surface area of thin al alloy plate

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP20488982A JPS5996274A (en) 1982-11-22 1982-11-22 Method for increasing surface area of thin al alloy plate

Publications (2)

Publication Number Publication Date
JPS5996274A JPS5996274A (en) 1984-06-02
JPH0156146B2 true JPH0156146B2 (en) 1989-11-29

Family

ID=16498070

Family Applications (1)

Application Number Title Priority Date Filing Date
JP20488982A Granted JPS5996274A (en) 1982-11-22 1982-11-22 Method for increasing surface area of thin al alloy plate

Country Status (1)

Country Link
JP (1) JPS5996274A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2723558B2 (en) * 1988-10-31 1998-03-09 松下冷機株式会社 Heat exchanger
JP4629930B2 (en) * 2000-08-24 2011-02-09 株式会社Adeka Etching solution for aluminum foil and method for etching aluminum foil

Also Published As

Publication number Publication date
JPS5996274A (en) 1984-06-02

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