JPS63195240A - Al brazing sheet - Google Patents
Al brazing sheetInfo
- Publication number
- JPS63195240A JPS63195240A JP2873387A JP2873387A JPS63195240A JP S63195240 A JPS63195240 A JP S63195240A JP 2873387 A JP2873387 A JP 2873387A JP 2873387 A JP2873387 A JP 2873387A JP S63195240 A JPS63195240 A JP S63195240A
- Authority
- JP
- Japan
- Prior art keywords
- core material
- brazing
- alloy
- brazing sheet
- grain size
- 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.)
- Pending
Links
- 238000005219 brazing Methods 0.000 title claims abstract description 31
- 239000011162 core material Substances 0.000 claims abstract description 33
- 229910045601 alloy Inorganic materials 0.000 claims abstract description 13
- 239000000956 alloy Substances 0.000 claims abstract description 13
- 229910018125 Al-Si Inorganic materials 0.000 claims abstract 3
- 229910018520 Al—Si Inorganic materials 0.000 claims abstract 3
- 229910018566 Al—Si—Mg Inorganic materials 0.000 claims abstract 3
- 239000000463 material Substances 0.000 claims description 13
- 239000013078 crystal Substances 0.000 claims description 6
- 238000005260 corrosion Methods 0.000 abstract description 17
- 230000007797 corrosion Effects 0.000 abstract description 16
- 229910052751 metal Inorganic materials 0.000 abstract description 7
- 239000002184 metal Substances 0.000 abstract description 7
- 238000005253 cladding Methods 0.000 abstract description 2
- 229910000838 Al alloy Inorganic materials 0.000 abstract 2
- 229910052802 copper Inorganic materials 0.000 abstract 2
- 230000001276 controlling effect Effects 0.000 abstract 1
- 230000001105 regulatory effect Effects 0.000 abstract 1
- 238000007747 plating Methods 0.000 description 13
- 230000000694 effects Effects 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 6
- 239000003507 refrigerant Substances 0.000 description 6
- 230000007423 decrease Effects 0.000 description 5
- 238000009792 diffusion process Methods 0.000 description 5
- 238000000034 method Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 238000007654 immersion Methods 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 239000000945 filler Substances 0.000 description 2
- 230000004907 flux Effects 0.000 description 2
- 238000000265 homogenisation Methods 0.000 description 2
- 230000001771 impaired effect Effects 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 101000993059 Homo sapiens Hereditary hemochromatosis protein Proteins 0.000 description 1
- 229910000861 Mg alloy Inorganic materials 0.000 description 1
- 238000010306 acid treatment Methods 0.000 description 1
- KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 description 1
- 238000012733 comparative method Methods 0.000 description 1
- 239000007771 core particle Substances 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- AWJWCTOOIBYHON-UHFFFAOYSA-N furo[3,4-b]pyrazine-5,7-dione Chemical compound C1=CN=C2C(=O)OC(=O)C2=N1 AWJWCTOOIBYHON-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B23—MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
- B23K—SOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
- B23K35/00—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting
- B23K35/22—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting characterised by the composition or nature of the material
- B23K35/24—Selection of soldering or welding materials proper
- B23K35/28—Selection of soldering or welding materials proper with the principal constituent melting at less than 950 degrees C
- B23K35/286—Al as the principal constituent
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明はAi製熟熱交換器ろう付けに使用するAJl製
プリプレージングシートするもので、特に熱交換器の耐
食性を改善するものである。[Detailed Description of the Invention] [Industrial Field of Application] The present invention is a pre-plating sheet made of AJI used for brazing an Ai heat exchanger, and particularly improves the corrosion resistance of the heat exchanger. .
一般に自動車のラジェーター、ヒーター及びクーラーの
コンデンサーやエバポレーター等の熱交換器は、Al製
プレージングシートからなる冷媒循環通路間にコルゲー
ト加工したAl製フィンを組合せ、ろう付けにより作ら
れている。Heat exchangers such as automobile radiators, condensers and evaporators for heaters and coolers are generally made by combining corrugated Al fins between refrigerant circulation passages made of Al plating sheets and brazing them together.
例えばドロンカップエバポレーターは第1図(イ)、(
ロ)に示すようにコルゲート加工したAi製ラフイン1
)とプレス成形したAl製プレージングシート(両面に
ろう材をクラッド)からなるプレスプレート(2)を図
に示すように積層し、ろう付けによりプレスプレート(
2)のろう材を溶融してフィン(1)とプレスプレート
(2)を接合すると共にプレスプレート(2)(2°)
間〈コア内部)に冷媒循環通路を形成している。For example, the Doron cup evaporator is shown in Figure 1 (a), (
Ai rough-in 1 corrugated as shown in b)
) and a press plate (2) consisting of a press-formed aluminum plating sheet (brazing metal clad on both sides) are laminated as shown in the figure, and the press plate (
2) Melt the brazing metal to join the fin (1) and press plate (2), and press plate (2) (2°)
A refrigerant circulation passage is formed between (inside the core).
ろう付は法としては塩化物系フラックスを使用する浸漬
ろう付は法と7ラツクスを使用しない真空ろう付は法が
主流をなし、浸漬ろう付は法ではプレージングシートに
JIS3003や6951合金等からなる芯材の両面又
は片面にAl−8i系のJI34343合金からなるろ
う材をクラッドしたものを用いている。また真空ろう付
は法ではプレージングシートにJIS 3003や69
51合金からなる芯材の両面又は片面にAl−3 i
−Mg系のJIS 4004合金ろう材をクラッドした
ものを用い、フィンに純AlやJIS 3003合金を
用いている。The main methods for brazing are immersion brazing, which uses chloride-based flux, and vacuum brazing, which does not use 7lux, and immersion brazing, which uses JIS 3003 or 6951 alloys for the plating sheet. The core material is clad with a brazing material made of Al-8i JI34343 alloy on both sides or one side. In addition, vacuum brazing is required by JIS 3003 and 69 for plating sheets.
Al-3 i on both sides or one side of the core material made of 51 alloy.
- A cladding of Mg-based JIS 4004 alloy brazing material is used, and pure Al or JIS 3003 alloy is used for the fins.
浸漬ろう付は法ではZnC1zを含むフラックスを用い
ることにより、熱交換器全体の表面にZn拡散層を形成
し、これが主要構成部(冷媒循環通路)の孔食発生を防
止している。また真空ろう付は法では材料的に特に犠牲
作用について同等考慮されていない。The immersion brazing method uses a flux containing ZnC1z to form a Zn diffusion layer on the entire surface of the heat exchanger, which prevents pitting corrosion in the main components (refrigerant circulation passages). In addition, vacuum brazing does not take into account sacrificial effects in terms of materials in the law.
エバポレーターでは表面に水分が凝縮するため、使用時
には表面が湿った環境にある。そのため真空ろう付は法
で作られたエバポレーターではろう付は後にクロム酸処
理等の防食対策がなされ、またフィンを形成する’M!
Alも冷媒循環通路を形成するJIS 3003や69
51に対し電位的に卑となって防食効果を示すも、フィ
ンから離れた部分では防食効果が期待できない。In an evaporator, moisture condenses on the surface, so the surface is in a moist environment when in use. Therefore, in the case of evaporators made by vacuum brazing, anti-corrosion measures such as chromic acid treatment are taken after brazing, and fins are formed.
Al also forms the refrigerant circulation passage JIS 3003 and 69
Although it becomes less noble in potential than 51 and exhibits an anticorrosive effect, no anticorrosive effect can be expected in the portions away from the fins.
一方冷媒循環通路を形成するプレージングシートの厚さ
は0.5〜0.6#程度であるが、軽量化のため一層の
薄肉化の要求があり、これに伴い強度向上および成形性
の維持が要求されている。成形性の尺度としては材料の
伸びを30%程度必要とするも、高強度材では伸びが著
しく低下し、プレス成形時に材料割れを起す。On the other hand, the thickness of the plating sheet that forms the refrigerant circulation passage is approximately 0.5 to 0.6 #, but there is a demand for thinner sheets to reduce weight, and with this, there is a need to improve strength and maintain formability. is required. As a measure of formability, elongation of the material is required to be about 30%, but in high-strength materials, elongation decreases significantly, causing material cracking during press forming.
本発明はこれに鑑み種々検討の結果、Ai製熟熱交換器
耐食性を向上するため、冷媒循環通路を形成する部材の
耐食性を向上するAi製プレージングシートを開発した
もので、CuO,3〜0.9wt%(以下wt%を単に
%と略記)、MrlO,5〜1.5%、3i0.2%以
下、FeO,2〜1.0%を含み、残部Alからなる合
金を芯材とし、その両面又は片面にAl−8i系又はA
l−5r−Mg系合金ろう材をクラッドし、芯材の結晶
粒度を50〜150μmとしたことを特徴とするもので
ある。In view of this, as a result of various studies, the present invention has developed an Al plating sheet that improves the corrosion resistance of members forming refrigerant circulation passages, in order to improve the corrosion resistance of aluminum heat exchangers. The core material is an alloy containing 0.9wt% (hereinafter wt% is simply abbreviated as %), MrlO, 5 to 1.5%, 3i0.2% or less, FeO, 2 to 1.0%, and the balance is Al. , Al-8i or A on both or one side
It is characterized by being clad with l-5r-Mg alloy brazing material and having a core material with a crystal grain size of 50 to 150 μm.
(作 用)
即ち本発明Ai製プレージングシートは上記構成からな
り、芯材を上記合金組成としたのは次の理由によるもの
である。(Function) That is, the Ai plating sheet of the present invention has the above structure, and the reason why the core material has the above alloy composition is as follows.
CLJは強度向上と電位貴化のために添加するもので、
その含有量を0.3〜0.9%と限定したのは、含有量
が0.3%未満では効果が少なく、0.9%を越えると
伸びが低下し、成形性を損なうためである。MnはCu
と同様強度向上と電位員化のために添加するもので、そ
の含有口を0.5〜1.5%と限定したのは、含有量が
0.5%未満では効果がなく、1.5%を越えると巨大
なA 1−M n化合物が生成し、成形性を損なうため
である。Siは結晶粒度を微細化すると共に強度向上の
ために添加するもので、その含有量を0,2%以下と限
定したのは、0.2%を越えて含有せしめる。と3i化
合物のカソードとしての働きにより耐孔食性を低下する
ためである。またFeは3ii様結晶粒度を微細化する
とともに強度向上のために添加するもので、その含有量
を0.2〜1.0%と限定したのは、0.2%未満では
効果がなく、1,0%を越えて含有せしめると、Fe化
合物のカソードとしての働きにより耐孔食性を低下する
ためである。CLJ is added to improve strength and noble potential.
The reason why the content was limited to 0.3 to 0.9% is that if the content is less than 0.3%, there will be little effect, and if it exceeds 0.9%, elongation will decrease and formability will be impaired. . Mn is Cu
Similarly, it is added to improve strength and increase electric potential, and the content is limited to 0.5 to 1.5% because it is ineffective if the content is less than 0.5%. %, a huge A 1-M n compound will be generated and the moldability will be impaired. Si is added to refine the crystal grain size and improve strength, and the content is limited to 0.2% or less when it is contained in excess of 0.2%. This is because pitting corrosion resistance is reduced due to the function of the 3i compound as a cathode. In addition, Fe is added to refine the 3ii-like grain size and improve strength, and the reason why its content is limited to 0.2 to 1.0% is because it is ineffective if it is less than 0.2%. This is because if the content exceeds 1.0%, the pitting corrosion resistance will decrease due to the Fe compound acting as a cathode.
次に芯材の結晶粒度を50〜150μmとしたのは、C
UやMnの添加のため伸びが低下して成形性が悪くなる
のを防止するためで、結晶粒度が50μm未満ではろう
付は加熱時のろう材の拡散が大きくなり、熱交換器コア
の座屈ヤ芯材厚さの低下を招き、150μ瓦を越えると
伸びの低下が著しいためである。通常プレージングシー
トはO材で使用される場合が多いが、H材についても芯
材粒度の範囲は同様とする。また芯材の結晶粒度のコン
トロールは芯材の均質化処理温度をコントロールするこ
とで行なわれ、高温はど細かく、Fe量が多いほど細か
くなる。Next, the crystal grain size of the core material was set to 50 to 150 μm because C
This is to prevent the elongation from decreasing due to the addition of U and Mn, which deteriorates the formability. If the crystal grain size is less than 50 μm, the brazing material will diffuse greatly during heating, and the seat of the heat exchanger core will deteriorate. This is because the thickness of the core material decreases, and if the thickness exceeds 150μ, the elongation decreases significantly. Normally, plating sheets are often used with O material, but the core particle size range is the same for H material as well. The crystal grain size of the core material is controlled by controlling the homogenization temperature of the core material; the higher the temperature, the finer the grain size, and the higher the amount of Fe, the finer the grain size.
第1表に示す芯材からなるプレージングシートを製造し
た。即ち第1表に示す組成の合金を60X 180 X
180 trm(D金型にl造し、600’CX3時
間均質化処理した後、両面面側して厚さ50!n!nと
した。一方ろう材はJ、IS 4004合金(Ai−1
0%3 i−1,5%My)を同様に鋳造後、面側して
500℃に加熱し、熱間圧延により厚さ10.5mの板
とした。これを上記芯材の両面に合せて500℃に加熱
し、熱間圧延圧着して厚さ5mの板とした。これを冷間
圧延して厚さ0.6mの板とし、360’CX2時間の
最終焼鈍を施してO材のプレージングシートを製造した
。プレージングシートの芯材の粒度は30〜140μm
であった。A plating sheet consisting of the core material shown in Table 1 was manufactured. That is, the alloy having the composition shown in Table 1 is 60X 180X
180 trm (D mold), after 600'C
0%3i-1.5%My) was cast in the same manner, heated face-side to 500°C, and hot-rolled into a plate with a thickness of 10.5 m. This was heated to 500° C. on both sides of the core material, and hot rolled and pressed to form a plate with a thickness of 5 m. This was cold rolled into a plate with a thickness of 0.6 m, and final annealed at 360'CX for 2 hours to produce a plating sheet of O material. The particle size of the core material of the praising sheet is 30 to 140 μm.
Met.
尚Nα7の芯材についてはNα1の組成の芯材を520
℃で均質化処理することにより芯材の粒度を170μ而
とした。For the core material of Nα7, the core material of the composition of Nα1 is 520
The particle size of the core material was made 170μ by homogenization treatment at ℃.
上記プレージングシートについて引張強さ及び伸びを測
定すると共に、成形性、耐食性及びろう材のろう付は後
の芯材への拡散状況を調べた。これ等の結果を第1表に
併記した。The tensile strength and elongation of the plating sheet were measured, and the moldability, corrosion resistance, and diffusion of the brazing material into the core material after brazing were also investigated. These results are also listed in Table 1.
成形性はJIS 2247A法に準じたエリクセン試験
により90s角に切断した試料について、直径20mm
の球頭ポンチで張出成形を行ない、亀裂が入るときの成
形高さを測定した。耐食性は5X10−5 torrの
真空中600℃で3分間真空ろう付けを行なった債、裏
面及び端面をシールして50X100 履の部分をキャ
ス試験に供し、200時間侵の最大孔食深さを比較した
。孔食深ざは深いものを10点選び出し、光学顕微鏡を
用いて焦点深度法により深さを求め、最も深いものにつ
いて断面を研摩して孔食深さを確認した。またろう材の
芯材への拡散状況はろう付は後の残留芯材厚さを測定し
た。Formability was measured using the Erichsen test according to the JIS 2247A method using samples cut into 90s squares with a diameter of 20mm.
Stretch molding was performed using a ball-head punch, and the molding height at which cracks appeared was measured. Corrosion resistance was determined by vacuum brazing the bond at 600°C for 3 minutes in a vacuum of 5 x 10-5 torr, sealing the back and edges, and subjecting the 50 x 100 shoe section to a CAST test to compare the maximum pitting depth after 200 hours of corrosion. did. Ten points with deep pitting corrosion depth were selected, the depth was determined by the depth of focus method using an optical microscope, and the depth of pitting corrosion was confirmed by polishing the cross section of the deepest one. In addition, the diffusion status of the brazing filler metal into the core material was determined by measuring the thickness of the remaining core material after brazing.
第1表から明らかなように本発明シートN(11〜6は
何れも引張強さ14KI/mrA以上、伸び26%以上
と中程度の強度と、エリクセン値9.4以上の成形性を
有し、孔食深ざは0.20s以下でろう材の芯材への拡
散も少ないことが判る。尚芯材の自然電位も安定して−
700mV (vs S、 C。As is clear from Table 1, the present invention sheets N (all 11 to 6 have a tensile strength of 14 KI/mrA or more, an elongation of 26% or more, which is a medium strength, and an Erichsen value of 9.4 or more, and formability). It can be seen that the depth of pitting corrosion is less than 0.20 s, and the diffusion of the brazing metal into the core material is also small.In addition, the natural potential of the core material is also stable.
700mV (vs S, C.
E)と犠牲作用にも十分効果が認められる。E) and the sacrificial effect are also sufficiently effective.
これに対し、本発明で規定する合金組成より外れる比較
シートNα7〜13は引張強さ、伸び。On the other hand, the comparative sheets Nα7 to Nα13, which deviate from the alloy composition specified by the present invention, have poor tensile strength and elongation.
エリクセン値、孔食深ざ、残留芯厚の何れか1つ以上が
劣ることが判る。即ち芯材粒度が150μmを越える比
較シートNα7及びCu含有量が多い比較法NQ9では
エリクセン値が低く、成形性が劣り、Cu含有量の少な
い比較シートNα8゜Mn含有量の少ない比較シートN
α10.Si含有量が多い比較シートNα12では何れ
も耐孔食性が劣り、Fe含有量の多い比較シートNα1
3ではろう材の芯材への拡散が大きいことが判る。尚M
n含有量の多い比較シートNα11は製造時にわれが発
生し、サンプルを取ることができなかつた。It can be seen that at least one of the Erichsen value, pitting depth, and residual core thickness is inferior. That is, the comparative sheet Nα7 with a core material particle size exceeding 150 μm and the comparative method NQ9 with a high Cu content have low Erichsen values and poor formability, and the comparative sheet Nα8 with a low Cu content and the comparative sheet N with a low Mn content
α10. Comparative sheet Nα12 with a high Si content has poor pitting corrosion resistance, while comparative sheet Nα1 with a high Fe content
It can be seen that in No. 3, the diffusion of the brazing filler metal into the core material is large. Nao M
Comparison sheet Nα11, which has a high n content, had cracks during production and could not be sampled.
このように本発明によればプレージングシートの耐孔食
性が著しく向上し、強度も従来シートより30%程度向
上するところから板厚を0.6履からo、 45711
11程度まで薄くすることが可能となり、Ai製熟熱交
換器耐食性を向上し、かつ軽量化を可能にする等工業上
顕著な効果を奏するものである。As described above, according to the present invention, the pitting corrosion resistance of the plating sheet is significantly improved, and the strength is also improved by about 30% compared to conventional sheets, so the plate thickness can be increased from 0.6 to 45711.
It is possible to reduce the thickness to about 11 mm, which has significant industrial effects, such as improving the corrosion resistance of the aluminum heat exchanger and making it possible to reduce the weight.
第1図(イ)、(ロ)はドロンカップエバポレーターの
一例を示すもので、(イ)は一部切欠いて示す斜視図、
(ロ)は側面図でおる。
1、フィン
2、プレスプレート
(イ)
(ロ)
一=i=
===:=
±
]Figures 1 (a) and (b) show an example of a Doron cup evaporator, and (a) is a partially cutaway perspective view;
(b) is a side view. 1, fin 2, press plate (a) (b) 1=i= ===:= ±]
Claims (1)
%,Si0.2wt%以下,Fe0.2〜1.0wt%
を含み、残部Alからなる合金を芯材とし、その両面又
は片面にAl−Si系又はAl−Si−Mg系合金ろう
材をクラッドし、芯材の結晶粒度を50〜150μmと
したことを特徴とするAl製ブレージングシート。Cu0.3-0.9wt%, Mn0.5-1.5wt
%, Si0.2wt% or less, Fe0.2-1.0wt%
The core material is an alloy containing the following: with the remainder being Al, and both or one side of the core material is clad with an Al-Si or Al-Si-Mg alloy brazing material, and the crystal grain size of the core material is 50 to 150 μm. Al brazing sheet.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2873387A JPS63195240A (en) | 1987-02-10 | 1987-02-10 | Al brazing sheet |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2873387A JPS63195240A (en) | 1987-02-10 | 1987-02-10 | Al brazing sheet |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS63195240A true JPS63195240A (en) | 1988-08-12 |
Family
ID=12256632
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2873387A Pending JPS63195240A (en) | 1987-02-10 | 1987-02-10 | Al brazing sheet |
Country Status (1)
Country | Link |
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JP (1) | JPS63195240A (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0339438A (en) * | 1989-07-05 | 1991-02-20 | Nikkei Giken:Kk | Pitting corrosion-resistant aluminum alloy and its manufacture |
WO1994022633A1 (en) * | 1993-04-06 | 1994-10-13 | Alcan International Limited | Aluminium alloy brazing sheet |
US5476725A (en) * | 1991-03-18 | 1995-12-19 | Aluminum Company Of America | Clad metallurgical products and methods of manufacture |
JP2001105175A (en) * | 1999-08-12 | 2001-04-17 | Pechiney Rhenalu | Drawing member for manufacturing heat exchanger and its manufacturing method |
WO2003076677A1 (en) * | 2002-03-08 | 2003-09-18 | Furukawa-Sky Aluminum Corp. | Method for producing aluminum alloy composite material for heat exchanger and aluminum alloy composite material |
JP2013199660A (en) * | 2012-03-23 | 2013-10-03 | Showa Denko Kk | Aluminum clad material for heat exchanger and method for producing the same |
JP2013204105A (en) * | 2012-03-29 | 2013-10-07 | Mitsubishi Alum Co Ltd | Plate material made of aluminum alloy |
JP2015054342A (en) * | 2013-09-12 | 2015-03-23 | 昭和電工株式会社 | Method for production of heat radiation device |
-
1987
- 1987-02-10 JP JP2873387A patent/JPS63195240A/en active Pending
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0339438A (en) * | 1989-07-05 | 1991-02-20 | Nikkei Giken:Kk | Pitting corrosion-resistant aluminum alloy and its manufacture |
US5476725A (en) * | 1991-03-18 | 1995-12-19 | Aluminum Company Of America | Clad metallurgical products and methods of manufacture |
US5669436A (en) * | 1991-03-18 | 1997-09-23 | Aluminum Company Of America | Method of continuously casting composite strip |
WO1994022633A1 (en) * | 1993-04-06 | 1994-10-13 | Alcan International Limited | Aluminium alloy brazing sheet |
AU692442B2 (en) * | 1993-04-06 | 1998-06-11 | Novelis Inc. | Aluminium alloy brazing sheet |
JP2011202279A (en) * | 1999-08-12 | 2011-10-13 | Constellium France | Drawn member for manufacturing heat exchanger, and method for manufacturing the same |
JP2001105175A (en) * | 1999-08-12 | 2001-04-17 | Pechiney Rhenalu | Drawing member for manufacturing heat exchanger and its manufacturing method |
WO2003076677A1 (en) * | 2002-03-08 | 2003-09-18 | Furukawa-Sky Aluminum Corp. | Method for producing aluminum alloy composite material for heat exchanger and aluminum alloy composite material |
CN1321217C (en) * | 2002-03-08 | 2007-06-13 | 古河Sky株式会社 | Method for producing aluminum alloy composite material for heat exchanger and aluminum alloy composite material |
CN100425726C (en) * | 2002-03-08 | 2008-10-15 | 古河Sky株式会社 | Method for producing aluminum alloy composite material for heat exchanger and aluminum alloy composite material |
JP2013199660A (en) * | 2012-03-23 | 2013-10-03 | Showa Denko Kk | Aluminum clad material for heat exchanger and method for producing the same |
JP2013204105A (en) * | 2012-03-29 | 2013-10-07 | Mitsubishi Alum Co Ltd | Plate material made of aluminum alloy |
JP2015054342A (en) * | 2013-09-12 | 2015-03-23 | 昭和電工株式会社 | Method for production of heat radiation device |
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