JPS5938319B2 - Method for manufacturing heat exchanger tubes - Google Patents
Method for manufacturing heat exchanger tubesInfo
- Publication number
- JPS5938319B2 JPS5938319B2 JP5374077A JP5374077A JPS5938319B2 JP S5938319 B2 JPS5938319 B2 JP S5938319B2 JP 5374077 A JP5374077 A JP 5374077A JP 5374077 A JP5374077 A JP 5374077A JP S5938319 B2 JPS5938319 B2 JP S5938319B2
- Authority
- JP
- Japan
- Prior art keywords
- tube
- metal
- heat exchanger
- heat
- boiling
- 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
Links
- 238000000034 method Methods 0.000 title claims description 12
- 238000004519 manufacturing process Methods 0.000 title claims description 9
- 229910052751 metal Inorganic materials 0.000 claims description 26
- 239000002184 metal Substances 0.000 claims description 26
- 239000008151 electrolyte solution Substances 0.000 claims description 12
- 238000012546 transfer Methods 0.000 claims description 12
- 229910000963 austenitic stainless steel Inorganic materials 0.000 claims description 5
- 239000002344 surface layer Substances 0.000 claims description 3
- 238000009835 boiling Methods 0.000 description 17
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 14
- 238000005260 corrosion Methods 0.000 description 7
- 230000007797 corrosion Effects 0.000 description 7
- 238000007747 plating Methods 0.000 description 7
- 229910001369 Brass Inorganic materials 0.000 description 6
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 6
- 239000010951 brass Substances 0.000 description 6
- 229910000831 Steel Inorganic materials 0.000 description 5
- 229910052804 chromium Inorganic materials 0.000 description 5
- 239000011651 chromium Substances 0.000 description 5
- 235000002639 sodium chloride Nutrition 0.000 description 5
- 239000010959 steel Substances 0.000 description 5
- 239000007788 liquid Substances 0.000 description 4
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 4
- 238000012545 processing Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000011148 porous material Substances 0.000 description 3
- 229910001220 stainless steel Inorganic materials 0.000 description 3
- 239000010935 stainless steel Substances 0.000 description 3
- 229910052725 zinc Inorganic materials 0.000 description 3
- 239000011701 zinc Substances 0.000 description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000005611 electricity Effects 0.000 description 2
- 238000005868 electrolysis reaction Methods 0.000 description 2
- 239000010410 layer Substances 0.000 description 2
- 150000001247 metal acetylides Chemical class 0.000 description 2
- 238000001000 micrograph Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229910052697 platinum Inorganic materials 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 239000006104 solid solution Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000010936 titanium Substances 0.000 description 2
- 229910052719 titanium Inorganic materials 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229910000936 Naval brass Inorganic materials 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 206010070834 Sensitisation Diseases 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910001566 austenite Inorganic materials 0.000 description 1
- 229910052728 basic metal Inorganic materials 0.000 description 1
- -1 basic metal salt Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 238000010828 elution Methods 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000008313 sensitization Effects 0.000 description 1
- 230000001235 sensitizing effect Effects 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 238000007751 thermal spraying Methods 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
Description
【発明の詳細な説明】
本発明は伝熱管の製造方法に関し、詳しくは加工が簡単
で安価な伝熱管の製造方法に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for manufacturing a heat exchanger tube, and more particularly to a method for manufacturing a heat exchanger tube that is easy to process and inexpensive.
伝熱管表面上でそれに接する液体を加熱沸騰させながら
伝熱を行なう所謂沸騰伝熱は、伝熱面への熱負荷を著し
く大きくでき相変化のない場合よりも伝勢が促進される
ので、このような現象を利用した伝熱管例えば沸騰伝熱
管又はヒートパイプ等の利用分野は極めて広汎にわたつ
ている。そして、更に、伝熱管の伝熱面上に、例えば沸
騰伝熱管においては管の外面に、又ヒートパイプにおい
ては管の内面に多孔質層を形成することによりいつそう
高い熱交換率が得られることも知られている。従来、こ
のような多孔層を形成する方法として例えば、焼結法、
塑性加工法、溶射法、メッキ法及び網巻法、更にはエッ
チングにより粗面を形成する方法等数多くの方法が提案
されているが、いずれも加工が煩雑で高価であるとか或
いは機能的に充分でないなどの欠点があつた。本発明の
目的は、前記の現状に鑑み、簡単な加工で大量生産に適
しかつ安価に製造しうる伝熱管の製造方法を提供するこ
とである。So-called boiling heat transfer, in which heat is transferred on the surface of a heat transfer tube by heating and boiling the liquid in contact with it, can significantly increase the heat load on the heat transfer surface and accelerate the transfer of heat compared to when there is no phase change. Heat exchanger tubes that utilize this phenomenon, such as boiling heat exchanger tubes or heat pipes, are used in an extremely wide range of fields. Furthermore, a higher heat exchange rate can be obtained by forming a porous layer on the heat transfer surface of the heat transfer tube, for example on the outer surface of the tube in a boiling heat transfer tube or on the inner surface of the tube in a heat pipe. It is also known that Conventionally, methods for forming such a porous layer include, for example, a sintering method,
Many methods have been proposed, including plastic processing, thermal spraying, plating, mesh wrapping, and etching to form a rough surface, but all of them are complicated and expensive, or are not functionally sufficient. There were some drawbacks, such as: In view of the above-mentioned current situation, an object of the present invention is to provide a method for manufacturing a heat exchanger tube that is suitable for mass production with simple processing and can be manufactured at low cost.
本発明について概説すれば、本発明の沸騰伝熱管の製造
方法は、金属管又は表面に金属をメッキした管を正極と
して電解質溶液中において該管を電解的に溶解し該管の
表面層を多孔質とすることを特徴とするものである。To summarize the present invention, the method for manufacturing a boiling heat exchanger tube of the present invention involves electrolytically dissolving the tube in an electrolyte solution using a metal tube or a tube whose surface is plated with metal as a positive electrode, and making the surface layer of the tube porous. It is characterized by its quality.
本発明の構成及び作用を添付図面により説明する。The structure and operation of the present invention will be explained with reference to the accompanying drawings.
第1図は本発明を実施するに当たり使用する実験装置の
概略図であり、第1図において目的物となる金属管1は
両端をプラグ2により密封し、電解質溶液3中に浸漬す
る。該溶液3中には負極4を設けかつ該金属管1が正極
となるように直流電源5と図示のように結線する。この
際、電流密度を均一にするために例えば沸騰伝熱管の場
合には負極4を中空円筒として正極の金属管1と同心に
配管することが望ましい。又、溶解速度即ち加工時間を
速めるために、電解質溶液3中に加熱器6を設けて適宜
加熱して温度調節を行なうとよい。本発明が適用できる
金属管としては、黄銅管あるいはオーステナイトステン
レス鋼管(例えば18−8ステンレス鋼)等のような各
種合金管が挙げられるが、金属管にメッキ(例えばクロ
ムメッキ)を施した管も適用可能である。電解質溶液と
しては、塩酸水溶液の使用が好適″ であるが、塩酸の
他に硫酸、硝酸、弗酸等の各種の酸又はこれらの酸とそ
の塩の混合物等を使用することができる。FIG. 1 is a schematic diagram of an experimental apparatus used to carry out the present invention. In FIG. 1, a metal tube 1, which is a target object, is sealed at both ends with plugs 2 and immersed in an electrolyte solution 3. A negative electrode 4 is provided in the solution 3 and connected to a DC power source 5 as shown so that the metal tube 1 becomes the positive electrode. At this time, in order to make the current density uniform, for example, in the case of a boiling heat exchanger tube, it is desirable that the negative electrode 4 be a hollow cylinder and arranged concentrically with the metal tube 1 of the positive electrode. Further, in order to speed up the dissolution rate, that is, the processing time, it is preferable to provide a heater 6 in the electrolyte solution 3 and appropriately heat it to adjust the temperature. Metal tubes to which the present invention can be applied include various alloy tubes such as brass tubes and austenitic stainless steel tubes (e.g., 18-8 stainless steel), but metal tubes with plating (e.g., chrome plating) may also be used. Applicable. As the electrolyte solution, it is preferable to use an aqueous solution of hydrochloric acid, but in addition to hydrochloric acid, various acids such as sulfuric acid, nitric acid, and hydrofluoric acid, or mixtures of these acids and their salts can also be used.
管材質が黄銅管の場合には、電解質溶液として塩酸と食
塩の混合水溶液が好適であり、電流を通・ すことによ
り黄銅中の亜鉛は電位差により選択的に溶出し、所謂”
脱亜鉛作用″が生起する。When the tube material is brass, a mixed aqueous solution of hydrochloric acid and common salt is suitable as the electrolyte solution, and by passing an electric current, the zinc in the brass is selectively eluted due to the potential difference, resulting in the so-called "
``Dezincification effect'' occurs.
即ち、電解質溶液3中に浸漬された黄銅管の表面では、
最初に塩基性の金属塩(塩化亜鉛)が生成し、これが仲
介となつて所謂7脱亜鉛作用7により金属の一部が電解
質溶液3中に少しづつ溶け出してくるが、金属管1が正
極となるように電流が通じられているためこの溶出速度
は著しく加速され、短時間で金属管表面は多孔質状とな
る。管材質が18Cr−8Ni等のオーステナイトステ
ンレス鋼管の場合には、前処理として鋼管表面の鋭敏化
熱処理を行なうのが好適である。That is, on the surface of the brass tube immersed in the electrolyte solution 3,
First, a basic metal salt (zinc chloride) is generated, and through this, a part of the metal gradually dissolves into the electrolyte solution 3 due to the so-called dezincification action 7. Since a current is passed through the metal tube, the elution rate is significantly accelerated, and the surface of the metal tube becomes porous in a short time. When the tube material is an austenitic stainless steel tube such as 18Cr-8Ni, it is preferable to perform a sensitizing heat treatment on the surface of the steel tube as a pretreatment.
すなわち、該管を予め400〜850℃に加熱後徐冷し
て粒界腐食感受性を与えておくとよい。周知のごとく、
このような前処理によりオーステナイト地中に過飽和に
固溶している炭素がクロムを主体とする炭化物(鉄及び
ニツケルの炭化物が含有される)として析出し、その結
果その隣接部のクロム量が粒内よりも少なくなるために
、電解腐食の条件によつてクロム欠乏部分が粒内よりも
優先的に腐食され易く、この電位域に保持された鋭敏化
鋼は粒界腐食されて多孔質となる。このようにして、オ
ーステナイトステンレス鋼の場合には、該管を正極とし
て粒界を優先的に腐食させることにより該管の表面を効
率的に多孔質とすることができる。この際、腐食処理後
に固溶体化処理をして組織を通常の状態に戻せば実用上
の支障はない。クロム等のメツキ管の場合には、メツキ
表面は元来微細な割れ目や小孔が生じており、平均に電
解的に溶解せず部分的に異なるので、電解的に溶解する
ことにより当然割れ目及び小孔の部分が早く溶解してこ
れが拡大されるわけである。That is, it is preferable to heat the pipe to 400 to 850° C. and then slowly cool it to impart intergranular corrosion susceptibility. As you know,
Through such pretreatment, the supersaturated solid solution of carbon in the austenite ground precipitates as carbides mainly composed of chromium (containing carbides of iron and nickel), and as a result, the amount of chromium in the adjacent areas decreases. Therefore, depending on the galvanic corrosion conditions, the chromium-deficient parts are more likely to be corroded preferentially than the inside of the grains, and sensitized steel held in this potential range undergoes intergranular corrosion and becomes porous. . In this way, in the case of austenitic stainless steel, the surface of the tube can be efficiently made porous by preferentially corroding the grain boundaries using the tube as a positive electrode. At this time, there is no practical problem if the structure is returned to its normal state by performing solid solution treatment after the corrosion treatment. In the case of plating pipes made of chromium, etc., the plating surface originally has minute cracks and small pores, and since it does not dissolve electrolytically on the average and differs locally, it is natural that cracks and pores will be formed by electrolytically dissolving it. The small pores dissolve quickly and become enlarged.
又、メツキ表面の応力の分布は一般に不均一であるため
、腐食が促進され割目が発生する。したがつて、多孔質
の空洞の大きさや有孔度、電圧は電流密度、浴温度及び
通電時間等によつて左右されるので、それらを適宜調整
することにより沸騰伝熱に最適な表面組織を得ることが
できる。以上の電解条件は通常、常温〜80℃の浴温度
、0.1〜100A/Dm2、程度の電流密度、数分〜
数時間の通電時間が適当であるが、これらの条件は伝熱
管材料や電解液の種類等により左右されるのは勿論であ
る。Furthermore, since the stress distribution on the plating surface is generally non-uniform, corrosion is accelerated and cracks occur. Therefore, the size, porosity, and voltage of porous cavities are affected by current density, bath temperature, current application time, etc., and by adjusting these appropriately, it is possible to obtain the optimal surface structure for boiling heat transfer. Obtainable. The above electrolysis conditions are usually a bath temperature of room temperature to 80°C, a current density of about 0.1 to 100 A/Dm2, and a few minutes to
A current application time of several hours is appropriate, but these conditions naturally depend on the material of the heat exchanger tube, the type of electrolyte, etc.
なお、本発明で使用する陰極としては、白金やチタン等
の電極が好適であるが、これらに限定されるものではな
い。The cathode used in the present invention is preferably an electrode made of platinum, titanium, or the like, but is not limited thereto.
又本発明は、円形断面の伝熱管に限らず矩形断面やフイ
ン付管などその他いかなる形状のものにも適用可能であ
る。本発明により電解的に溶解された金属表面は、能率
的な核沸騰(伝熱面上の特定点即ち核から連続的に発生
してカク乱作用を起す蒸気泡による沸騰状態をいう)に
適した微小な空洞から成る海面状組織となつており、本
発明によれば、このような金属管又は金属メツキ管を簡
単な加工で安価かつ大量に製造することができる。Further, the present invention is applicable not only to heat exchanger tubes having a circular cross section but also to any other shape such as a rectangular cross section or a finned tube. The metal surface electrolytically melted according to the present invention is suitable for efficient nucleate boiling (a boiling state caused by vapor bubbles that are continuously generated from a specific point, that is, a nucleus, on a heat transfer surface and cause a disturbance effect). According to the present invention, such metal tubes or metal-plated tubes can be manufactured in large quantities at low cost through simple processing.
したがつて本発明は工業上極めて有用なものである。次
に本発明を実施例により説明するが、本発明はこれによ
りなんら限定されるものではない。Therefore, the present invention is extremely useful industrially. Next, the present invention will be explained with reference to examples, but the present invention is not limited thereto in any way.
実施例 1銅約60%、亜鉛約40%の組成を有する黄
銅(ネーバル黄銅管)管を、約60℃に維持した塩酸と
食塩の混合水溶液(水1000CCに食塩約1009及
び36%濃度の塩酸約10CCを加えたもの)中で黄銅
片を正極とし白金を負極とし、電圧約1V1電流密度約
2A/Dm2で約15分間電解して亜鉛を溶解し脱亜鉛
処理を行なつた。Example 1 A brass (naval brass tube) pipe having a composition of about 60% copper and about 40% zinc was prepared with a mixed aqueous solution of hydrochloric acid and common salt maintained at about 60°C (1000 cc of water with about 1009 cc of salt and hydrochloric acid with a concentration of 36%). The brass piece was used as the positive electrode and the platinum was used as the negative electrode in a sample containing about 10 cc (approximately 10 cc) of electrolysis at a voltage of about 1V and a current density of about 2A/Dm2 for about 15 minutes to dissolve zinc and perform dezincification treatment.
その結果、第2図の顕微鏡写真(倍率400倍)に見ら
れるような部分的に溶解された表面を有する金属管が得
られた。写真中光つた部分はピットを合わせた所、ぼけ
ている部分は該部より高い所又は低い所を示す。この写
真から明らかなように、脱亜鉛された金属表面は能率的
な核沸騰に適した微小な空洞からなる海綿状組織となつ
ていることがわかる。実施例 2
鋼管の外面に、周知の方法により厚さ約0.27111
1のクロムメツキを施した管を正極とし、銅を負極とし
、電解質溶液として36%塩酸300CCを水700C
Cに溶解したものを使用し、液温約70℃、電圧約3、
電流密度約3A/Dm2で約15分間通電して、メツキ
皮膜の一部を電解的に溶解した。The result was a metal tube with a partially melted surface as seen in the micrograph of FIG. 2 (400x magnification). In the photo, the bright areas indicate the areas where the pits are combined, and the blurred areas indicate areas higher or lower than that area. As is clear from this photo, the dezinced metal surface has a spongy structure consisting of minute cavities suitable for efficient nucleate boiling. Example 2 The outer surface of a steel pipe was coated with a thickness of about 0.27111 mm by a well-known method.
The chrome-plated tube from step 1 is used as the positive electrode, copper is used as the negative electrode, and 300 cc of 36% hydrochloric acid and 700 cc of water are used as the electrolyte solution.
Use a solution dissolved in C, the liquid temperature is about 70℃, the voltage is about 3,
Electricity was applied for about 15 minutes at a current density of about 3 A/Dm2 to electrolytically dissolve a part of the plating film.
その結果第3図に示すような縦断面を有する金属管が得
られた。即ち、鋼管壁7に鍍金したクロム8は、図示の
ように微少な空洞からなる海綿状組織となり、核沸騰に
適した表面組織をしていることがわかる。実施例 3
18Cr−8Niオーステナイトステンレス鋼管を約7
00℃に加熱後徐冷して鋭敏化処理を行なつた後、該管
を正極としチタンを負極とし、電解質溶液として36%
塩酸300CCを水700CCに溶解したものを使用し
、液温約50℃、電圧約1V1電流密度約1A/Dm2
で約30分通電して粒界腐食処理を行なつた。As a result, a metal tube having a vertical cross section as shown in FIG. 3 was obtained. That is, it can be seen that the chromium 8 plated on the steel pipe wall 7 has a spongy structure consisting of minute cavities as shown in the figure, and has a surface structure suitable for nucleate boiling. Example 3 18Cr-8Ni austenitic stainless steel pipe with approximately 7
After heating to 00°C and slowly cooling to perform sensitization treatment, the tube was used as a positive electrode and titanium was used as a negative electrode, and a 36% electrolyte solution was used.
Using 300 cc of hydrochloric acid dissolved in 700 cc of water, the liquid temperature is about 50°C, the voltage is about 1 V, the current density is about 1 A/Dm2.
The grain boundary corrosion treatment was carried out by applying electricity for about 30 minutes.
その結果、第4図の顕微鏡写真(倍率400倍)に見ら
れるような部分的に溶解された表面を有する金属管が得
られた。なお、写真において、白色部は焦点が合つてい
る部分で、焦点深度の異なる凹凸部はぼけて示されてい
る。このように、金属表面は能率的な核沸騰に適した多
孔質組織となつている。実施例 4
実施例3と同様な処理方法(但し、電解条件は、温度:
常温、電圧:0.5〜0.1V1電流密度:0.5〜0
.05A/Dm2、通電時間:約18時間、電解質溶液
:実施例1と同じ)により粒界腐食を行なつた。As a result, a metal tube with a partially melted surface as seen in the micrograph of FIG. 4 (400x magnification) was obtained. In the photograph, white parts are in focus, and uneven parts with different depths of focus are shown out of focus. In this way, the metal surface has a porous structure suitable for efficient nucleate boiling. Example 4 The same treatment method as Example 3 (however, the electrolytic conditions were: temperature:
Room temperature, voltage: 0.5-0.1V1 current density: 0.5-0
.. Intergranular corrosion was carried out using 05A/Dm2, current application time: about 18 hours, electrolyte solution: same as in Example 1).
得られた多孔質ステンレス鋼管の表面の凹凸を、管軸に
沿つた直線上で測定した記録を第5図に示す。第5図に
みられるように、この管表面の凹凸深度は約10〜30
μmでピツチは約0.1〜0.15顧の多孔質組織であ
る。この伝熱管の内側から電熱加熱により約17000
Kca1/M2hrの熱流量を与えて、水中及びフレオ
ンR−11中(何れも外気温度22℃において液面は大
気開放の条件)で沸騰させた場合の気泡の発生状況をそ
れぞれ観察した、気泡は管表面の多数の核から多量かつ
均密に発生し、極めて能率的な核沸騰を行なつているこ
とが観察された。なお、この実験において、対照として
未処理のステンレス鋼管について同一条件における気泡
の発生状況を観察したところ、格段の差が認められた。
以上述べたように、本発明によれば、簡易かつ安価に沸
騰伝熱に適した表面が多孔質の金属管又は表面に金属を
メツキした管を製造でき、しかも伝熱面の空洞の大きさ
及び有孔度も用途に応じて適宜調整することができるの
で、本発明は特に沸騰伝熱管、ヒートパイプの大量生産
に適している。FIG. 5 shows a record of measurements of the surface irregularities of the obtained porous stainless steel tube on a straight line along the tube axis. As seen in Figure 5, the depth of the unevenness on the tube surface is approximately 10 to 30
It is a porous structure with a pitch of about 0.1 to 0.15 μm. Approximately 17,000
We observed the formation of bubbles when boiling in water and in Freon R-11 (both at an outside temperature of 22°C and the liquid level open to the atmosphere) with a heat flow of Kca1/M2hr. It was observed that nucleate boiling was generated uniformly in large quantities from many nuclei on the tube surface, and that nucleate boiling was extremely efficient. In addition, in this experiment, when the generation of bubbles was observed under the same conditions for an untreated stainless steel pipe as a control, a marked difference was observed.
As described above, according to the present invention, it is possible to easily and inexpensively manufacture a metal tube with a porous surface suitable for boiling heat transfer, or a tube whose surface is plated with metal, and the size of the cavity on the heat transfer surface is small. Since the porosity and the porosity can be adjusted as appropriate depending on the application, the present invention is particularly suitable for mass production of boiling heat exchanger tubes and heat pipes.
図面は本発明の実施態様の具体例を示すものであり、第
1図は本発明を実施するに当たり使用した実験装置の概
略図、第2図は実施例1により得られた金属面の顕微鏡
写真、第3図は実施例2により得られた金属管表層の縦
断面図、第4図は実施例3により得られた金属面の顕微
鏡写真、第5図は実施例4により得られた金属管の表面
を管軸に沿つた表線上で測定した記録図を示す。
符号は次のものを示す。
1・・・・・・金属管、2・・・・・・プラグ、3・・
・・・・電解質溶液、4・・・・・・陰極、5・・・・
・・直流電源、6・・・・・・加熱器、7・・・・・・
鋼管壁、8・・・・・・メツキクロム。The drawings show specific examples of embodiments of the present invention, and FIG. 1 is a schematic diagram of the experimental equipment used to carry out the present invention, and FIG. 2 is a microscopic photograph of the metal surface obtained in Example 1. , FIG. 3 is a vertical cross-sectional view of the surface layer of the metal tube obtained in Example 2, FIG. 4 is a microscopic photograph of the metal surface obtained in Example 3, and FIG. 5 is the metal tube obtained in Example 4. This shows a record of the surface of the tube measured on the surface line along the tube axis. The symbols indicate the following. 1...Metal pipe, 2...Plug, 3...
... Electrolyte solution, 4 ... Cathode, 5 ...
...DC power supply, 6... Heater, 7...
Steel pipe wall, 8...Metsukichrome.
Claims (1)
電解質溶液中において該管を電解的に溶解し該管の表面
層を多孔質とすることを特徴とする伝熱管の製造方法。 2 オーステナイトステンレス管を400〜850℃で
熱処理、徐冷後電解的に溶解する特許請求の範囲第1項
記載の方法。[Claims] 1. A heat transfer tube characterized in that the tube is electrolytically dissolved in an electrolyte solution using a metal tube or a tube whose surface is plated with metal as a positive electrode to make the surface layer of the tube porous. Production method. 2. The method according to claim 1, wherein the austenitic stainless steel tube is heat treated at 400 to 850°C, slowly cooled, and then electrolytically melted.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5374077A JPS5938319B2 (en) | 1977-05-12 | 1977-05-12 | Method for manufacturing heat exchanger tubes |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5374077A JPS5938319B2 (en) | 1977-05-12 | 1977-05-12 | Method for manufacturing heat exchanger tubes |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS53138969A JPS53138969A (en) | 1978-12-04 |
| JPS5938319B2 true JPS5938319B2 (en) | 1984-09-14 |
Family
ID=12951209
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP5374077A Expired JPS5938319B2 (en) | 1977-05-12 | 1977-05-12 | Method for manufacturing heat exchanger tubes |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5938319B2 (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62112996A (en) * | 1985-11-11 | 1987-05-23 | Mitsubishi Metal Corp | Heat-transmitting body |
| JP2595167B2 (en) * | 1992-06-12 | 1997-03-26 | 高橋金物株式会社 | Hinge |
| AU2791797A (en) * | 1996-05-23 | 1997-12-09 | Toyo Kohan Co. Ltd. | Plated steel plate for battery cases, method of manufacturing the same, battery case and battery |
-
1977
- 1977-05-12 JP JP5374077A patent/JPS5938319B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS53138969A (en) | 1978-12-04 |
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