JPH04100674A - Production of brazing sheet for flux brazing - Google Patents
Production of brazing sheet for flux brazingInfo
- Publication number
- JPH04100674A JPH04100674A JP6464590A JP6464590A JPH04100674A JP H04100674 A JPH04100674 A JP H04100674A JP 6464590 A JP6464590 A JP 6464590A JP 6464590 A JP6464590 A JP 6464590A JP H04100674 A JPH04100674 A JP H04100674A
- Authority
- JP
- Japan
- Prior art keywords
- brazing
- flux
- brazing sheet
- sheet
- etching
- 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
Links
- 238000005219 brazing Methods 0.000 title claims abstract description 66
- 230000004907 flux Effects 0.000 title claims abstract description 36
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 12
- 239000000463 material Substances 0.000 claims abstract description 22
- 238000005530 etching Methods 0.000 claims abstract description 21
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 6
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims abstract description 6
- 229910021364 Al-Si alloy Inorganic materials 0.000 claims abstract 2
- 238000011282 treatment Methods 0.000 claims description 20
- 238000000137 annealing Methods 0.000 claims description 15
- 238000000034 method Methods 0.000 claims description 8
- 238000005096 rolling process Methods 0.000 claims description 4
- 239000012670 alkaline solution Substances 0.000 claims description 2
- 239000007788 liquid Substances 0.000 abstract description 4
- 230000003472 neutralizing effect Effects 0.000 abstract description 4
- 238000005260 corrosion Methods 0.000 abstract description 3
- 230000007797 corrosion Effects 0.000 abstract description 3
- 238000005253 cladding Methods 0.000 abstract description 2
- 230000003247 decreasing effect Effects 0.000 abstract 2
- 239000011162 core material Substances 0.000 description 16
- 238000004140 cleaning Methods 0.000 description 11
- 229910045601 alloy Inorganic materials 0.000 description 10
- 239000000956 alloy Substances 0.000 description 10
- 238000006386 neutralization reaction Methods 0.000 description 8
- 238000012733 comparative method Methods 0.000 description 6
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 5
- 229910017604 nitric acid Inorganic materials 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- 239000007789 gas Substances 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 229910000679 solder Inorganic materials 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000003513 alkali Substances 0.000 description 3
- 239000000945 filler Substances 0.000 description 3
- 239000011261 inert gas Substances 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 2
- 229910000676 Si alloy Inorganic materials 0.000 description 2
- 239000003990 capacitor Substances 0.000 description 2
- 238000005097 cold rolling Methods 0.000 description 2
- 150000002222 fluorine compounds Chemical class 0.000 description 2
- 230000009972 noncorrosive effect Effects 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- 239000010731 rolling oil Substances 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000005098 hot rolling Methods 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000003507 refrigerant Substances 0.000 description 1
- 239000011856 silicon-based particle Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
Landscapes
- ing And Chemical Polishing (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明はフラックスろう付用ブレージングシートの製造
方法に関し、特にろう付性を向上させたものである。DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a method for manufacturing a brazing sheet for flux brazing, and particularly to a method for improving brazing properties.
従来自動車用熱交換器を製造する際に実施するフラック
スろう付には、一般にJIS 3003合金。JIS 3003 alloy is generally used for flux brazing when manufacturing heat exchangers for automobiles.
JIS 3005合金又はJIS 6951合金の芯材
の表面にAO−Si系合金であるJIS 4343合金
やJIS 4045合金からなるろう材をクラッドした
ブレージングシートが使用されている。そして一般に上
記熱交換器のプレート材としては厚さが0.5〜21n
In、フィン材としては厚さが0.1〜0.2mmの材
料が使用されている。A brazing sheet is used in which the surface of a core material of JIS 3005 alloy or JIS 6951 alloy is clad with a brazing material made of JIS 4343 alloy or JIS 4045 alloy, which is an AO-Si alloy. Generally, the plate material of the heat exchanger has a thickness of 0.5 to 21 nm.
In, a material having a thickness of 0.1 to 0.2 mm is used as the fin material.
例えばラジェーターを例に取ると、第1図に示すように
ゴムパツキン(9)を介して樹脂タンクQ(Itを取り
付けるヘッダー(8)材には片面にろう材をクラッドし
た板厚1.6mmのブレージングシートが、そして冷媒
が流通するチューブ(7)材には片面にろう材をクラッ
ドした板厚0.4mmのブレージングシートを電縫加工
したものが用いられている。又フィン(6)材にはJI
S 5XXX系合金からなり板厚0.1++onのベア
材が使用されている。For example, taking a radiator as an example, as shown in Figure 1, the header (8) to which the resin tank Q (It is attached via the rubber gasket (9)) is made of a 1.6 mm thick brazing plate clad with brazing filler metal on one side. The material of the tube (7) through which the sheet and the refrigerant flow is made of a brazing sheet with a thickness of 0.4 mm clad with brazing metal on one side and subjected to electric resistance welding.The material of the fin (6) is J.I.
A bare material made of S5XXX alloy with a plate thickness of 0.1++ on is used.
ところでフラックスろう付性の中で、最近フッ化物系の
非腐食性フラックスを使用して大気圧の不活性ガス中で
ろう付加熱するろう仁王法が普及している。その理由は
、第1にフラックス濃度が3wt%程度であって、塩化
物系フラックスを使用する従来のろう仁王法の場合の5
0〜60wt%と比較して極端に低濃度であり、フラッ
クス使用量が少ないのでコスト低減の効果があるからで
ある。また第2の理由は、このフッ化物系フラックスを
用いたろう仁王法によれば、ろう付後にアルミ表面に残
留するフラックス残渣がアルミに対して非腐食性である
のでフラックス残渣の除去が不必要なためである。By the way, among the flux brazing properties, the brazing method, which uses a fluoride-based non-corrosive flux and performs brazing heating in an inert gas at atmospheric pressure, has recently become popular. The reason for this is first that the flux concentration is about 3wt%, which is 5% compared to the conventional wax method using chloride flux.
This is because the concentration is extremely low compared to 0 to 60 wt%, and the amount of flux used is small, which is effective in reducing costs. The second reason is that according to the brazing method using this fluoride flux, the flux residue remaining on the aluminum surface after brazing is non-corrosive to the aluminum, so there is no need to remove the flux residue. It's for a reason.
これに対して従来の塩化物系フラックスを使用した場合
は、ろう付後に湯洗、硝酸洗浄等の洗浄処理が必要であ
り、公害の面からも問題であった。On the other hand, when conventional chloride-based fluxes are used, cleaning treatments such as hot water washing and nitric acid washing are required after brazing, which is also a problem in terms of pollution.
〔発明が解決しようとする課題〕
しかしながらこのフッ化物系フラックスは水に不溶であ
るため、上記のように低濃度のフラックスをブレージン
グシートの表面に均一に塗布するのは困難であった。こ
れはブレージングシートの表面が、圧延油分の付着で撥
水性を呈することも均一塗布をより困難なものとする原
因になっていた。[Problems to be Solved by the Invention] However, since this fluoride flux is insoluble in water, it is difficult to uniformly apply a low concentration flux to the surface of the brazing sheet as described above. This is because the surface of the brazing sheet exhibits water repellency due to adhesion of rolling oil, which also makes uniform application more difficult.
これに対処するため、実際にはフラックス濃度を若干高
めにしたり、フラックス液中に界面活性剤を添加するこ
とにより、フラックスの付着量を多くしてろう付性を確
保していた。To deal with this, in practice, the flux concentration was increased slightly or a surfactant was added to the flux liquid to increase the amount of flux deposited and ensure brazability.
しかしこのようにフラックスの付着量を多くするとコス
ト面で不利となってしまい、さらにこのためにろう付後
にフラックス残渣が多くなるが、残渣量が多いと塗装性
や耐食性等が低下するばかりでなく、熱交換器のフィン
のルーバ一部やフィレット部等のようにフラックスが凝
集し易い部分では、残渣の塊が発生して通気抵抗が増加
して熱交換性能が低下する等の問題も生じてしまう。However, increasing the amount of flux deposited in this way is disadvantageous in terms of cost, and this also results in a large amount of flux residue after brazing, which not only reduces paintability and corrosion resistance, but also In areas where flux tends to aggregate, such as the louvers and fillets of heat exchanger fins, residue clumps occur, increasing ventilation resistance and reducing heat exchange performance. Put it away.
また不活性ガス中でのろう付に際しては、酸化性ガスで
あるH2Oは露点−40°C以下、02は11000p
p以下に規制する必要かあり、雰囲気の変動によるろう
付性の低下も問題であった。In addition, when brazing in an inert gas, the dew point of H2O, which is an oxidizing gas, is -40°C or less, and the dew point of 02 is 11000p.
It is necessary to regulate the temperature to below p, and there is also a problem of deterioration in brazing properties due to changes in the atmosphere.
本発明はこれに鑑み種々検討の結果、プレーングシート
表面をエツチング及び中和することにより、表面の汚れ
や酸化皮膜を除去してフラックスろう付性に優れるブレ
ージングシートを提供するもので、特に表面の清浄化に
より使用フラックス量の低減と、ろう付写囲気中の酸化
性ガスの規制緩和を実現したものである。In view of this, as a result of various studies, the present invention provides a brazing sheet that has excellent flux brazing properties by removing surface dirt and oxide film by etching and neutralizing the surface of the plain sheet. This reduces the amount of flux used and eases regulations on oxidizing gases in the brazing atmosphere.
即ち本発明は、AQ−Si合金をろう材としてクラッド
したアルミニウム製ブレージングシートの製造において
、その表面をアルカリ溶液にて0.01−1.5g/m
”エツチングし、その後中和処理することを特徴とする
ものであり、工・ソチング処理をブレージングシートの
最終焼鈍前に行うこと、又はエツチング処理をブレージ
ングシートの圧延・焼鈍工程の終了後に行うことは有効
である。That is, in the production of an aluminum brazing sheet clad with AQ-Si alloy as a brazing material, the surface of the sheet is coated with an alkaline solution at 0.01-1.5 g/m
``It is characterized by etching and then neutralization treatment, and the etching treatment is performed before the final annealing of the brazing sheet, or after the rolling and annealing process of the brazing sheet is completed. It is valid.
このようにアルカリエツチング量を0.01〜5g/a
+2としたのは、O,O1g/m2未満ではろう付性改
善の効果がなく、また5 g/m2を超えるとブレージ
ングシート表面からのSi粒子の脱落が顕著になって表
面の凹凸が増加し、ろう付性が低下するからである。そ
してアルカリエツチングは30〜70°Cの温度で濃度
が1〜5%のNaOH水溶液等で処理すればよい。In this way, the amount of alkaline etching is 0.01 to 5 g/a.
The reason why it was set as +2 is that if it is less than 1 g/m2 of O, there is no effect of improving brazing properties, and if it exceeds 5 g/m2, Si particles will drop off from the surface of the brazing sheet and the surface unevenness will increase. This is because the brazing properties deteriorate. Alkaline etching may be carried out at a temperature of 30 to 70 DEG C. with an aqueous NaOH solution having a concentration of 1 to 5%.
またアルカリエツチング後には、スマットの除去や中和
を目的として水洗、硝酸洗浄を行う必要がある。このス
マットの除去や中和処理は室温で5〜30%濃度の硝酸
水溶液で処理すればよいが、硝酸洗浄の前後には室温の
水道水にて水洗する必要がある。After alkaline etching, it is necessary to wash with water and nitric acid for the purpose of removing and neutralizing smut. This smut removal and neutralization treatment may be carried out at room temperature with a nitric acid aqueous solution having a concentration of 5 to 30%, but it is necessary to wash with tap water at room temperature before and after washing with nitric acid.
さらに上記洗浄処理は浸漬あるいはスプレーにて実施す
ればよいが、圧延コイルを連続処理するにはエッチング
力、中和力の強いスプレー洗浄を採用すればライン速度
を高速化することが可能となる。Further, the above-mentioned cleaning treatment may be carried out by dipping or spraying, but in order to continuously treat rolled coils, it is possible to increase the line speed by employing spray cleaning which has strong etching power and neutralizing power.
そして上記水処理後は80〜150°Cで乾燥してブレ
ージングシート表面に水分を残留させないことが重要で
ある。After the water treatment, it is important to dry the brazing sheet at 80 to 150°C so that no moisture remains on the surface of the brazing sheet.
また上記のエツチング処理を最終焼鈍前に行う理由は次
の通りである。The reason why the above etching treatment is performed before the final annealing is as follows.
即ち熱間圧延、冷間圧延を経たブレージングシートの表
面には、圧延油残渣やアルミニウム摩耗粉等が多量に付
着しており、このまま焼鈍すると油分の焼付や汚れの焼
付等が発生して表面性状は著しく劣化する。そこで最終
の焼鈍前に洗浄することにより、これらの表面異物を除
去できるので焼鈍による変化としては皮膜厚さの若干の
増加だけである。なお焼鈍雰囲気を0□及びH2020
量低く抑えた焼鈍ガス中で行えば、皮膜厚さの増加は最
低限とすることが可能である。そしてこの処理は焼なま
し材であるO材(調質材)の製造に適している。In other words, a large amount of rolling oil residue and aluminum abrasion powder adheres to the surface of a brazing sheet that has been hot-rolled or cold-rolled, and if annealed in this state, oil and dirt will seize and the surface quality will deteriorate. deteriorates significantly. Therefore, by cleaning before the final annealing, these surface foreign substances can be removed, so that the only change due to annealing is a slight increase in the film thickness. The annealing atmosphere is 0□ and H2020.
If the annealing is carried out in a low amount of annealing gas, the increase in film thickness can be minimized. This treatment is suitable for producing O material (tempered material), which is an annealed material.
また上記エツチング処理を圧延、焼鈍後に行えば、焼鈍
により焼付いた油分や汚れ等を容易に取り除くことがで
きる。しがし上記最終焼鈍前のエツチング処理と比較し
て、この場合のエツチング量は多くする必要がある。そ
してこの処理は焼鈍後冷間圧延を加えるH材(調質材)
の製造に適している。Furthermore, if the above-mentioned etching treatment is performed after rolling and annealing, it is possible to easily remove oil, dirt, etc. that have been baked in by the annealing. However, compared to the etching treatment before the final annealing described above, the amount of etching in this case needs to be larger. This treatment involves cold rolling after annealing (H material).
suitable for manufacturing.
次に本発明の実施例について説明する。 Next, examples of the present invention will be described.
〈実施例1〉
JIS 4045合金ろう材をJIS 3003合金芯
材の両面に10%の厚さでクラッドしたブレージングシ
ートの製造に際し、熱間合わせ圧延でクラツド材の厚さ
を5mmとし、続いて冷間圧延で0.5mmの厚さとし
た後、第1表に示す条件でアルカリ洗浄を行った。その
後360’CX 2 Hrの最終焼鈍を不活性ガス中で
行って、0.6mm厚さの0材を得た。なおアルカリ洗
浄後のスマット除去・中和処理は次の工程で実施した。<Example 1> When manufacturing a brazing sheet in which JIS 4045 alloy filler metal was clad on both sides of a JIS 3003 alloy core material to a thickness of 10%, the thickness of the clad material was made 5 mm by hot rolling, and then cold rolling was performed. After rolling to a thickness of 0.5 mm, alkali cleaning was performed under the conditions shown in Table 1. Thereafter, a final annealing of 360'CX 2 Hr was performed in an inert gas to obtain a 0.6 mm thick zero material. Note that smut removal and neutralization treatment after alkali cleaning were performed in the following steps.
即ち
(室温×30秒)(60°CX30秒)(90℃X10
秒)そして洗浄前後の重量を測定してエツチング量を算
出し、また以下のようにして耐圧強度と外側のろう切れ
発生状況を調べ、これらの結果を第1表に示した。That is, (room temperature x 30 seconds) (60°C x 30 seconds) (90°C x 10 seconds)
The weight before and after washing was measured to calculate the amount of etching, and the pressure resistance and occurrence of solder breakage on the outside were investigated as follows. The results are shown in Table 1.
即ち上記各条件でアルカリ洗浄、即ちエツチング処理し
たブレージングシートにより、第2図に示したような、
中央部を開口させて排気口(2)としたカップ成形品(
1)を製作した。そしてフラックスとしてK AQF
、やに、AQF、等からなるフッ化物系フラックスを2
%の濃度で作り、上記カップ成形品に1枚づつ別々に塗
布して150°Cで乾燥した後、第3図に示すようにこ
れらカップ成形品(1)を互い違いに積層して3個の中
空構造体(3)が排気口(2)で連通した中空容器の形
状に組付け、さらに上端のカップ成形品(1)の排気口
(2)に耐圧試験機接続口(5)を取り付けた。そして
この中空容器を露点−60°Cで02量が9ooppm
のN2ガス雰囲気中にて595°Cに加熱してろう付を
実施して一体化し、それぞれのエツチング処理条件毎に
5個の一体化中空容器(以下コアと記す)を作製した。That is, by using a brazing sheet that has been subjected to alkali cleaning, that is, etching treatment under each of the above conditions, as shown in FIG.
Cup molded product with an opening in the center and an exhaust port (2)
1) was produced. And as a flux K AQF
, resin, AQF, etc.
% concentration, applied to each of the cup molded products separately and dried at 150°C, and then stacked these cup molded products (1) alternately to form three cup molded products, as shown in Figure 3. The hollow structure (3) was assembled into a hollow container shape that communicated with the exhaust port (2), and the pressure tester connection port (5) was attached to the exhaust port (2) of the cup molded product (1) at the upper end. . Then, store this hollow container at a dew point of -60°C and the amount of 02 is 9ooppm.
They were heated to 595° C. in a N2 gas atmosphere to perform brazing and integrate, and five integrated hollow containers (hereinafter referred to as cores) were produced for each etching treatment condition.
そしてこれらコアについて、目視にて外側のろう切れを
調べて1個のコアに1ケ所以上のろう切れが発生すれぼ
ろう切れ有りとし、がっ5個中何個のコアにろう切れが
発生したかを記した。These cores were visually inspected for solder breaks on the outside, and if one or more cores had one or more breaks in the solder, it was determined that there was a break in the wax, and how many of the five cores had breaks in the wax. I wrote down the following.
また接続口(5)から高圧空気を導入して5個のコアの
耐圧強度を調べてその平均値を記した。In addition, high-pressure air was introduced through the connection port (5), and the pressure strength of the five cores was examined, and the average value was recorded.
なお上記中空容器の最下段のカップ成形品は孔なしカッ
プ成形品(4)である。Note that the cup molded product at the bottom of the hollow container is a cup molded product without holes (4).
第1表から明らかなように、本発明法によるコアの耐圧
強度は何れも38kgG/ci以上であり、かつろう切
れもなく優れたろう付性を示した。As is clear from Table 1, the compressive strength of the cores produced by the method of the present invention was all 38 kgG/ci or more, and they exhibited excellent brazing properties without any brazing breakage.
これに対してエツチング量の少ない比較法No、 6に
よるコア、硝酸中和の無い比較法N098によるコア及
びアルカリ洗浄の無い比較法No、 9によるコアは3
4〜35kgG/cd程度の耐圧強度しかなく、さらに
ろう切れも発生していた。またエツチング量の多い比較
法No、 7は耐圧強度は比較的高いがろう切れが発生
していた。On the other hand, cores made by Comparative Method No. 6 with a small amount of etching, cores made by Comparative Method No. 9 without nitric acid neutralization, and cores made by Comparative Method No. 9 without alkaline cleaning are 3.
The pressure resistance was only about 4 to 35 kgG/cd, and wax breakage also occurred. Comparative method No. 7, which had a large amount of etching, had relatively high pressure resistance, but cracking of the solder occurred.
〈実施例2〉
JIS 4343合金ろう材をJIS 3003合金芯
材の両面に10%の厚さでクラッドしたブレージングシ
ートからなるフィン材の製造に際し、クラツド材を熱間
合わせ圧延して厚さを5mmとし、その後冷間圧延を施
して0.20mmの板厚とした後360℃X2Hrの中
間焼鈍を施し、さらに冷間圧延を行って厚さ0.16m
+aのフィン材とし、しかる後第2表に示す各条件でア
ルカリ洗浄を行った。<Example 2> When manufacturing a fin material consisting of a brazing sheet in which JIS 4343 alloy brazing filler metal is clad on both sides of a JIS 3003 alloy core material to a thickness of 10%, the cladding material is hot-rolled to a thickness of 5 mm. After that, it was cold rolled to a thickness of 0.20 mm, then intermediate annealed at 360°C for 2 hours, and further cold rolled to a thickness of 0.16 mm.
+a fin material was used, and then alkaline cleaning was performed under each condition shown in Table 2.
なおその後中和処理を実施したものについての中和処理
条件は、実施例1と同一とした。Note that the neutralization treatment conditions for those that were subsequently subjected to neutralization treatment were the same as in Example 1.
そして実施例1と同様にエツチング量を算出してその結
果を第2表に併記した。Then, the etching amount was calculated in the same manner as in Example 1, and the results are also listed in Table 2.
また第4図に示すようにこれら各条件のフィンσDをコ
ルゲート加工したものと、JIS 1050材押出チユ
ーブ(2)を組み合わせたコンデンサーミニコアを作製
し、その後実施例1と同様のフッ化物系フラックスを濃
度1%で塗布し、実施例1と同一条件でろう付を実施し
た。In addition, as shown in Fig. 4, a capacitor mini core was prepared by combining the corrugated fin σD under these conditions with a JIS 1050 material extruded tube (2), and then the same fluoride flux as in Example 1 was used. was applied at a concentration of 1%, and brazing was performed under the same conditions as in Example 1.
そして第4図に示す各ミニコアのフィン口υと押出チュ
ーブ(2)との接合であるコルゲートフィン山αりの1
00個あたりのろう付良好な接合部の山数を調べ、その
山数の全山数に占める割合を接合率として計算し、その
結果を第2表に併記した。And 1 of the corrugated fin mountain α, which is the connection between the fin opening υ of each mini-core and the extruded tube (2) shown in Fig. 4.
The number of ridges of joints with good brazing per 00 pieces was investigated, and the ratio of the number of ridges to the total number of ridges was calculated as the bonding rate, and the results are also listed in Table 2.
第2表から判るように、本発明法によるフィン材を用い
たミニコアについては、フィンの接合率は何れも95%
以上であって、低濃度フラックスという苛酷なろう付条
件であっても良好な接合性を示した。これに対してアル
カリ洗浄の無い比較法No、17及び洗浄の不十分な比
較法N。As can be seen from Table 2, for the mini cores using the fin material according to the present invention, the fin bonding rate was 95%.
As described above, good bondability was exhibited even under severe brazing conditions using low concentration flux. On the other hand, Comparative Method No. 17 without alkaline cleaning and Comparative Method N with insufficient cleaning.
、14によるものはフラックス液がフィン表面に十分濡
れないために、接合率は85%と低く、また中和処理の
無いNo、 16は特に接合率が悪かった。, No. 14 had a low bonding rate of 85% because the flux liquid did not sufficiently wet the fin surface, and No. 16, which had no neutralization treatment, had a particularly poor bonding rate.
このように本発明により、ろう付材料に中和処理を併用
する中程度のアルカリエツチングを施すことにより、表
面皮膜の除去やフラックス液の濡れ性の向上が図れるの
でろう付性が向上する。そして本発明によればフラック
スの使用量を低減することが可能となり、またこれによ
ってフラックス残渣が減少するので塗装性、耐食性及び
熱交換性能などが向上する等顕著な効果を奏する。As described above, according to the present invention, by subjecting the brazing material to moderate alkaline etching combined with neutralization treatment, the surface film can be removed and the wettability of the flux liquid can be improved, thereby improving brazing properties. According to the present invention, it is possible to reduce the amount of flux used, and as a result, flux residue is reduced, resulting in significant effects such as improvement in paintability, corrosion resistance, heat exchange performance, etc.
第1図はラジェーターを一部切欠いた斜視図、第2図(
イ)(ロ)はろう付試験用のカップ成形品をしめすもの
で(イ)は平面図、(ロ)は(イのYY線断面図、第3
図はカップ成形品を組み合わせた耐圧試験用中空容器の
側断面図、第4図はろう付試験用のコンデンサーのミニ
コアを示す斜視図である。
■
カップ成形品
排気口
中空構造体
孔なしカップ成形品
耐圧試験機接続口
フィン
チューブ
ヘッダー
ゴムパツキン
樹脂タンク
押出チューブ
コルゲートフィン山
第1図
第2図Figure 1 is a partially cutaway perspective view of the radiator, Figure 2 (
A) (B) shows a cup molded product for brazing test. (A) is a plan view, (B) is a cross-sectional view along the YY line of
The figure is a side sectional view of a hollow container for pressure resistance tests in which cup molded products are combined, and FIG. 4 is a perspective view showing a mini-core of a capacitor for brazing tests. ■ Cup molded product exhaust port Hollow structure No hole Cup molded product Pressure tester Connection port Fin tube Header Rubber packing Resin tank Extruded tube Corrugated fin mountain Figure 1 Figure 2
Claims (3)
ミニウム製ブレージングシートの製造において、その表
面をアルカリ溶液にて0.01〜5g/m^2エッチン
グし、その後中和処理することを特徴とするフラックス
ろう付用ブレージングシートの製造方法。(1) In manufacturing an aluminum brazing sheet clad with Al-Si alloy as a brazing material, the surface is etched with an alkaline solution of 0.01 to 5 g/m^2, and then neutralized. A method for producing brazing sheets for flux brazing.
前に行う請求項(1)記載のフラックスろう付用ブレー
ジングシートの製造方法。(2) The method for producing a brazing sheet for flux brazing according to claim (1), wherein the etching treatment is performed before final annealing of the brazing sheet.
鈍工程の終了後に行う請求項(1)記載のフラックスろ
う付用ブレージングシートの製造方法。(3) The method for producing a brazing sheet for flux brazing according to claim (1), wherein the etching treatment is performed after the rolling and annealing process of the brazing sheet is completed.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2064645A JP2783893B2 (en) | 1990-03-15 | 1990-03-15 | Method of manufacturing brazing sheet for flux brazing |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2064645A JP2783893B2 (en) | 1990-03-15 | 1990-03-15 | Method of manufacturing brazing sheet for flux brazing |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH04100674A true JPH04100674A (en) | 1992-04-02 |
JP2783893B2 JP2783893B2 (en) | 1998-08-06 |
Family
ID=13264199
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2064645A Expired - Lifetime JP2783893B2 (en) | 1990-03-15 | 1990-03-15 | Method of manufacturing brazing sheet for flux brazing |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2783893B2 (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2660043A1 (en) * | 2012-05-04 | 2013-11-06 | Hydro Aluminium Rolled Products GmbH | Aluminium compound material for flux free soldering |
WO2015086802A1 (en) | 2013-12-13 | 2015-06-18 | Hydro Aluminium Rolled Products Gmbh | Flux-free joining of aluminum composite materials |
WO2017060236A1 (en) | 2015-10-05 | 2017-04-13 | Hydro Aluminium Rolled Products Gmbh | Aluminum composite material for use in thermal flux-free joining methods and method for producing same |
WO2017060234A1 (en) | 2015-10-05 | 2017-04-13 | Hydro Aluminium Rolled Products Gmbh | Aluminum composite material for use in thermal flux-free joining methods and method for producing same |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0289590A (en) * | 1988-09-26 | 1990-03-29 | Mitsubishi Alum Co Ltd | Brazing material and brazing method |
-
1990
- 1990-03-15 JP JP2064645A patent/JP2783893B2/en not_active Expired - Lifetime
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0289590A (en) * | 1988-09-26 | 1990-03-29 | Mitsubishi Alum Co Ltd | Brazing material and brazing method |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2660043A1 (en) * | 2012-05-04 | 2013-11-06 | Hydro Aluminium Rolled Products GmbH | Aluminium compound material for flux free soldering |
WO2013164466A1 (en) | 2012-05-04 | 2013-11-07 | Hydro Aluminium Rolled Products Gmbh | Aluminium composite material for flux-free soldering |
WO2015086802A1 (en) | 2013-12-13 | 2015-06-18 | Hydro Aluminium Rolled Products Gmbh | Flux-free joining of aluminum composite materials |
US10773325B2 (en) | 2013-12-13 | 2020-09-15 | Hydro Aluminium Rolled Products Gmbh | Flux-free joining of aluminium composite materials |
WO2017060236A1 (en) | 2015-10-05 | 2017-04-13 | Hydro Aluminium Rolled Products Gmbh | Aluminum composite material for use in thermal flux-free joining methods and method for producing same |
WO2017060234A1 (en) | 2015-10-05 | 2017-04-13 | Hydro Aluminium Rolled Products Gmbh | Aluminum composite material for use in thermal flux-free joining methods and method for producing same |
Also Published As
Publication number | Publication date |
---|---|
JP2783893B2 (en) | 1998-08-06 |
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