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JPH0312151B2 - - Google Patents
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JPH0312151B2 - - Google Patents

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Publication number
JPH0312151B2
JPH0312151B2 JP9296080A JP9296080A JPH0312151B2 JP H0312151 B2 JPH0312151 B2 JP H0312151B2 JP 9296080 A JP9296080 A JP 9296080A JP 9296080 A JP9296080 A JP 9296080A JP H0312151 B2 JPH0312151 B2 JP H0312151B2
Authority
JP
Japan
Prior art keywords
heat transfer
transfer surface
aluminum
treatment liquid
mol
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
JP9296080A
Other languages
Japanese (ja)
Other versions
JPS5719397A (en
Inventor
Toshimitsu Uchama
Eizo Isoyama
Masayuki Kaji
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.)
Altemira Co Ltd
Original Assignee
Showa Aluminum Corp
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 Showa Aluminum Corp filed Critical Showa Aluminum Corp
Priority to JP9296080A priority Critical patent/JPS5719397A/en
Publication of JPS5719397A publication Critical patent/JPS5719397A/en
Publication of JPH0312151B2 publication Critical patent/JPH0312151B2/ja
Granted legal-status Critical Current

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  • Chemical Treatment Of Metals (AREA)
  • Electrochemical Coating By Surface Reaction (AREA)

Description

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

この発明は、アルミニウム製熱交換器の凝縮伝
熱面(この明細書で単に「伝熱面」とは凝縮伝熱
面をいう)における親水性付与方法に関する。 この明細書において、「アルミニウム」という
用語は、純アルミニウム、少量の不純物を含む市
販のアルミニウムおよびアルミニウムがその大部
分を占めるアルミニウム合金を含むものとする。 一般にアルミニウム製熱交換器の凝縮伝熱面、
たとえば凝縮器として用いられる熱交換器の媒体
流通管の内面において、凝縮を伴う熱交換性能を
高めるには、凝縮により生じた液の層を通して未
凝縮蒸気のエネルギーを奪う必要があることか
ら、上記凝縮液の層をできるだけ薄くする必要が
ある。そのためこのような凝縮面は液との親水
性、すなわちヌレ性の良好なものであることが要
望せられる。また他の凝縮伝熱面、すなわちカ
ー・クーラー、ルーム・クーラー等の空気調和機
の蒸発器として用いられる熱交換器のフイン表面
においては、フインの表面温度が大気の露点以下
となるためフインの表面に水滴が付着し、このよ
うな水滴の付着により通風抵抗が増大し、かつ風
量が減少して熱交換効率が低下する。これは蒸発
器の性能向上と小型化のためにフインピツチを狭
くした場合にとくに顕著に現われる。熱交換効率
はフインのヌレ性、すなわち親水性が大きく影響
するものであり、フイン方面のヌレ性が良いと付
着した水が水滴となりにくく、このため通風抵抗
が小さくなり、風量も多くなつて熱交換効率も向
上する。このような観点から、従来より機械的な
いし化学的に凝縮伝熱面を粗面化したり、種々の
形状に加工したり、さらには焼結合金層を形成し
たりする工夫がなされているが、これらはいずれ
も熱交換性能、品質の安全性および製造コストの
点に難点があり、さらに腐食の点でも問題がある
上に、水との反応による水素ガスの発生のために
熱伝達性能が低下するものであつたため、未だ工
業的に実用化されるに到つていない。 この発明は、アルミニウム製熱交換器の凝縮伝
熱面に優れた親水性を簡単に付与することのでき
る方法を提供することを目的とする すなわち、この発明の方法は、アルカリ金属、
アルカリ土類金属またはそれらの塩を1または2
種以上と、シリカゾルとを含有する処理液でアル
ミニウム製熱交換器の凝縮伝熱面を化成処理する
ことを特徴とする、アルミニウム製熱交換器の凝
縮伝熱面における親水性付与方法である。 上記化成処理によつてアルミニウム材表面に形
成された化成皮膜が伝熱面を構成する。 アルカリ金属およびアルカリ土類金属は、周期
律表中のいずれの金属であつてもよい。特にリチ
ウム、ナトリウム、カリウム、マグネシウム、カ
ルシウム、ストロンチウムが好ましい。塩の形態
も特に限定されないが、通常は塩化物、ヨウ化物
などのハロゲン化物、硫酸塩、硝酸塩、炭酸塩、
シユウ酸塩などがよく用いられる。上記金属およ
びそれらの塩はアルミニウム表面に化成皮膜を形
成するための必須成分である。そしてこれは単独
で、または数種類を併用して用いられる。後者の
場合には特に均一でかつ厚い皮膜を形成すること
ができる。処理液における上記金属またはそれら
の塩の濃度は0.005〜2モル/の範囲にある。
その理由は、濃度が0.005モル/未満の場合に
は、皮膜の形成が十分に進まず、また2モル/
を越えても、皮膜形成能はことさら向上せず、か
えつて処理液中に金属水酸化物が沈澱して液の安
定性が悪くなるからである。蒸発伝熱面を形成す
る場合には、表面の粗面化が必要であることか
ら、塩の濃度は比較的高目の方がよく、特に0.1
〜1モル/が好ましい。また凝縮伝熱面を形成
する場合には、皮膜は蒸発伝熱面の場合より薄い
方がよく、そのため濃度は0.01〜0.2モル/が
好ましい。 シリカゾルは、形成された伝熱面の耐食性を向
上する作用をなす。シリカゾルの濃度はSiO2
して0.0001〜0.5%の範囲にある。その理由は濃
度が0.0001%未満では耐食性が乏しく、0.5%を
越えると皮膜の生成が阻害されるからである。特
に好ましい濃度は0.003〜0.3モル/である。 また、処理液には、アルミン酸ナトリウム、ア
ルミン酸カリウムなどのアルミン酸塩を添加する
こともある。アルミン酸塩は、皮膜形成を促進す
るとともに皮膜の凝集力を向上して均一な皮膜を
得るのに寄与する。アルミン酸塩の濃度は0.001
〜1.0モル/の範囲にある。その理由は、濃度
が0.001モル/未満ではアルミン酸塩による上
記効果が発揮されず、1.0モルを越えると沈澱物
が生じるからである。特に好ましい濃度は0.01〜
0.3モル/である。 さらに、処理液にはトリエタノールアミンのよ
うなアミン類を添加することもある。アミン類は
処理液の安定性を向上して金属水酸化物の沈澱を
防ぐ作用を果す。 処理液の温度は40℃以上が好ましい。温度が40
℃未満では皮膜形成が十分になされない。処理液
のPHは6〜13が好ましい。PHが6未満では皮膜の
形成よりもアルミニウムの溶解の方がより進行し
てしまい、皮膜が生成しにくくなる。 処理液の調製に用いられる建浴水は、脱イオン
水、蒸溜水のほか水道水、地下水のように種々の
イオンを含有する水であつてもよい。 処理時間は、処理液の濃度とも関連するが、通
常1〜60分である。これ以上長くても皮膜形成効
果は特に向上しない。蒸発伝熱面を形成するに
は、高濃度の処理液を用いて、比較的長時間処理
を行う。他方凝縮伝熱面を形成するには、低濃度
の処理液を用いて、比較的短時間処理を行う。 なお、この発明による伝熱面の形成方法は、エ
ツチング、ブラストなどの化学的ないし機械的処
理によるアルミニウム表面の粗面化や、ローレツ
ト加工、切削加工などの溝形成加工の後に行う
と、一層効果的である。 以上の次第で、この発明によれば、アルミニウ
ム材表面の粗面化により伝熱面積が大きくかつ耐
食性に優れた伝熱面を形成することができる。か
くして、ち密でかつ液体とのヌレ性の良好な酸化
物ないし水和酸化物層を形成することができる。
さらにこの発明によれば、従来処理の困難であつ
た管内面に対しても容易に処理を施すことがで
き、したがつて管の内外面を同時に処理すること
ができて極めて作業性が良い。しかも処理は1段
階でなされるためこの点でも作業性が良い。 実施例 1〜5 熱交換器の凝縮伝熱面のアルミニウム材として
JISA1100−H24製のもの(大きさ1mm×50mm×
100mm)を用い、これを以下の条件で処理液に浸
漬した。
The present invention relates to a method for imparting hydrophilicity to a condensing heat transfer surface (in this specification, the term "heat transfer surface" simply refers to a condensing heat transfer surface) of an aluminum heat exchanger. In this specification, the term "aluminum" is intended to include pure aluminum, commercially available aluminum with minor impurities, and aluminum alloys in which aluminum predominates. Generally the condensing heat transfer surface of aluminum heat exchangers,
For example, in order to improve the heat exchange performance with condensation on the inner surface of the medium flow pipe of a heat exchanger used as a condenser, it is necessary to remove energy from uncondensed vapor through a layer of liquid produced by condensation. It is necessary to make the layer of condensate as thin as possible. Therefore, such a condensing surface is required to have good hydrophilicity with the liquid, that is, good wettability. In addition, on other condensation heat transfer surfaces, that is, on the surface of the fins of heat exchangers used as evaporators in air conditioners such as car coolers and room coolers, the surface temperature of the fins is below the dew point of the atmosphere. Water droplets adhere to the surface, and the adhesion of such water droplets increases ventilation resistance and reduces the air volume, resulting in a decrease in heat exchange efficiency. This becomes especially noticeable when the fin pitch is narrowed to improve the performance and downsize the evaporator. Heat exchange efficiency is greatly influenced by the wettability of the fins, that is, their hydrophilicity.If the wettability of the fins is good, the adhering water will be less likely to form droplets, which will reduce ventilation resistance and increase the amount of air, which will increase the heat transfer efficiency. Exchange efficiency is also improved. From this point of view, efforts have been made to mechanically or chemically roughen the condensation heat transfer surface, process it into various shapes, and even form a sintered alloy layer. All of these have drawbacks in terms of heat exchange performance, quality safety, and manufacturing cost.Furthermore, they have problems in terms of corrosion, and heat transfer performance deteriorates due to the generation of hydrogen gas due to reaction with water. Because of this, it has not yet been put into practical use industrially. An object of the present invention is to provide a method that can easily impart excellent hydrophilicity to the condensing heat transfer surface of an aluminum heat exchanger.
1 or 2 alkaline earth metals or their salts
This is a method for imparting hydrophilicity to a condensing heat transfer surface of an aluminum heat exchanger, the method comprising chemically treating the condensing heat transfer surface of an aluminum heat exchanger with a treatment liquid containing a silica sol and a silica sol. A chemical conversion film formed on the surface of the aluminum material by the above chemical conversion treatment constitutes a heat transfer surface. The alkali metal and alkaline earth metal may be any metal in the periodic table. Particularly preferred are lithium, sodium, potassium, magnesium, calcium, and strontium. The form of the salt is not particularly limited, but it usually includes halides such as chlorides and iodides, sulfates, nitrates, carbonates,
Oxalates are often used. The above metals and their salts are essential components for forming a chemical conversion film on the aluminum surface. These can be used alone or in combination. In the latter case, a particularly uniform and thick film can be formed. The concentration of the above-mentioned metals or their salts in the treatment liquid is in the range of 0.005 to 2 mol/mole.
The reason for this is that if the concentration is less than 0.005 mol/mol, the film formation will not proceed sufficiently, and if the concentration is less than 2 mol/mol/
This is because, even if the amount exceeds 1, the film-forming ability is not particularly improved, and on the contrary, metal hydroxides are precipitated in the treatment solution, resulting in worsening of the stability of the solution. When forming an evaporative heat transfer surface, it is necessary to roughen the surface, so it is better to have a relatively high salt concentration, especially 0.1
~1 mol/ is preferred. Furthermore, when forming a condensing heat transfer surface, it is better for the film to be thinner than in the case of an evaporative heat transfer surface, and therefore the concentration is preferably 0.01 to 0.2 mol/. The silica sol functions to improve the corrosion resistance of the formed heat transfer surface. The concentration of silica sol is in the range of 0.0001-0.5% as SiO2 . The reason for this is that if the concentration is less than 0.0001%, corrosion resistance is poor, and if it exceeds 0.5%, film formation is inhibited. A particularly preferred concentration is 0.003 to 0.3 mol/. Further, an aluminate salt such as sodium aluminate or potassium aluminate may be added to the treatment liquid. Aluminate promotes film formation and improves the cohesive force of the film, contributing to obtaining a uniform film. The concentration of aluminate is 0.001
It is in the range of ~1.0 mol/. The reason for this is that if the concentration is less than 0.001 mol/mol, the above effect of the aluminate will not be exhibited, and if it exceeds 1.0 mol/mol, a precipitate will form. Particularly preferred concentration is 0.01~
It is 0.3 mol/. Furthermore, amines such as triethanolamine may be added to the treatment liquid. The amines serve to improve the stability of the treatment solution and prevent precipitation of metal hydroxides. The temperature of the treatment liquid is preferably 40°C or higher. temperature is 40
If the temperature is lower than ℃, sufficient film formation will not occur. The pH of the treatment liquid is preferably 6 to 13. If the pH is less than 6, the dissolution of aluminum will proceed faster than the formation of a film, making it difficult to form a film. The prepared bath water used for preparing the treatment liquid may be water containing various ions such as deionized water, distilled water, tap water, and ground water. The treatment time is related to the concentration of the treatment liquid, but is usually 1 to 60 minutes. Even if the length is longer than this, the film forming effect will not be particularly improved. To form the evaporative heat transfer surface, a highly concentrated treatment liquid is used and the treatment is performed for a relatively long time. On the other hand, in order to form a condensing heat transfer surface, a treatment is performed for a relatively short time using a treatment liquid of low concentration. Note that the method for forming a heat transfer surface according to the present invention is more effective when performed after roughening the aluminum surface by chemical or mechanical treatment such as etching or blasting, or after groove forming processing such as knurling or cutting. It is true. As described above, according to the present invention, a heat transfer surface having a large heat transfer area and excellent corrosion resistance can be formed by roughening the surface of the aluminum material. In this way, an oxide or hydrated oxide layer that is dense and has good wettability with liquid can be formed.
Further, according to the present invention, it is possible to easily treat the inner surface of the tube, which has conventionally been difficult to treat, and therefore the inner and outer surfaces of the tube can be treated simultaneously, resulting in extremely high workability. Moreover, since the processing is performed in one step, workability is also good in this respect. Examples 1 to 5 As an aluminum material for the condensing heat transfer surface of a heat exchanger
Made of JISA1100-H24 (size 1mm x 50mm x
100 mm) and was immersed in the treatment solution under the following conditions.

【表】【table】

【表】 こうして形成した伝熱面について、経過日数と
接触角の関係を求めた。結果を図面に示す。また
比較のために、上記アルミニウム材と同じ材料を
30℃にて2分間クロメート処理したもの(比較例
1)、同アルミニウム材を5%NaOH溶液で50℃
にて3分間処理し、30%HNO3で脱脂したもの
(比較例2)、同アルミニウム材を陽極酸化処理し
蒸気処理したもの(比較例3)についても上記関
係を求めた。これら結果を同図に示す。図からわ
かるように、実施例により形成した伝熱面は、比
較例により形成したものに比べて接触角が小さ
く、したがつて優れたヌレ性を有する。しかもこ
のヌレ性は長期にわたつて劣化することがない。
[Table] Regarding the heat transfer surface thus formed, the relationship between the number of days elapsed and the contact angle was determined. The results are shown in the drawing. For comparison, the same material as the aluminum material above was used.
Chromate treated at 30℃ for 2 minutes (Comparative Example 1), same aluminum material treated with 5% NaOH solution at 50℃
The above relationship was also determined for the aluminum material treated for 3 minutes and degreased with 30% HNO 3 (Comparative Example 2), and the same aluminum material anodized and steam treated (Comparative Example 3). These results are shown in the figure. As can be seen from the figure, the heat transfer surface formed according to the example has a smaller contact angle than that formed according to the comparative example, and therefore has excellent wetting properties. Moreover, this wettability does not deteriorate over a long period of time.

【図面の簡単な説明】[Brief explanation of drawings]

図面は経過日数と接触角の関係を示すグラフで
ある。
The drawing is a graph showing the relationship between elapsed days and contact angle.

Claims (1)

【特許請求の範囲】 1 アルカリ金属、アルカリ土類金属またはそれ
らの塩を1または2種以上と、シリカゾルとを含
有する処理液でアルミニウム製熱交換器の凝縮伝
熱面を化成処理することを特徴とする、アルミニ
ウム製熱交換器の凝縮伝熱面における親水性付与
方法。 2 処理液がさらにアルミン酸塩を含む特許請求
の範囲第1項記載の方法。 3 処理液がさらにアミン類を含む特許請求の範
囲第1項または第2項記載の方法。
[Scope of Claims] 1. A process for chemically treating the condensing heat transfer surface of an aluminum heat exchanger with a treatment liquid containing one or more alkali metals, alkaline earth metals, or their salts and silica sol. A method for imparting hydrophilicity to the condensing heat transfer surface of an aluminum heat exchanger. 2. The method according to claim 1, wherein the treatment liquid further contains an aluminate. 3. The method according to claim 1 or 2, wherein the treatment liquid further contains an amine.
JP9296080A 1980-07-07 1980-07-07 Formation of heating surface on aluminum material Granted JPS5719397A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9296080A JPS5719397A (en) 1980-07-07 1980-07-07 Formation of heating surface on aluminum material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9296080A JPS5719397A (en) 1980-07-07 1980-07-07 Formation of heating surface on aluminum material

Publications (2)

Publication Number Publication Date
JPS5719397A JPS5719397A (en) 1982-02-01
JPH0312151B2 true JPH0312151B2 (en) 1991-02-19

Family

ID=14069001

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9296080A Granted JPS5719397A (en) 1980-07-07 1980-07-07 Formation of heating surface on aluminum material

Country Status (1)

Country Link
JP (1) JPS5719397A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3077193B2 (en) * 1990-11-23 2000-08-14 株式会社デンソー Method of forming corrosion resistant chemical conversion coating on aluminum surface
JP5083578B2 (en) * 2010-09-15 2012-11-28 株式会社イネックス Aluminum substrate with enhanced cooling effect by far-infrared high radiation coating and method for producing the same

Also Published As

Publication number Publication date
JPS5719397A (en) 1982-02-01

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