JPH04128333A - Te-and p-added brass excellent in corrosion - Google Patents
Te-and p-added brass excellent in corrosionInfo
- Publication number
- JPH04128333A JPH04128333A JP24953290A JP24953290A JPH04128333A JP H04128333 A JPH04128333 A JP H04128333A JP 24953290 A JP24953290 A JP 24953290A JP 24953290 A JP24953290 A JP 24953290A JP H04128333 A JPH04128333 A JP H04128333A
- Authority
- JP
- Japan
- Prior art keywords
- weight
- brass
- corrosion
- grain size
- corrosion resistance
- 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.)
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Links
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は、復水器、加水加熱器、蒸留器、冷却器、遣水
装置等の熱交換器用の材料として、特に、自動車等に用
いられるラジェーターのチューブ材として好適な、耐腐
食性に優れた黄銅に関するものである。[Detailed Description of the Invention] [Industrial Application Field] The present invention is used as a material for heat exchangers such as condensers, water heaters, distillers, coolers, water supply devices, etc., particularly for automobiles, etc. This invention relates to brass with excellent corrosion resistance, which is suitable as a tube material for radiators.
[従来の技術]
従来、ラジェーターのチューブ材としては、黄銅、ある
いはこれに微量のPが添加された銅合金が一般的に利用
されて来ており、特に、機械的性質や成型性の面で優れ
た特性を発揮すると共に、他の銅合金に比較して安価に
て入手出来る事から、黄銅が広く用いられて来た。[Prior Art] Conventionally, brass or a copper alloy to which a small amount of P is added has been generally used as a tube material for a radiator, and it has particularly good mechanical properties and formability. Brass has been widely used because it exhibits excellent properties and can be obtained at a lower price than other copper alloys.
しかし乍、近年に於ける様に、上記の機器を利用する領
域の拡大と、これを利用する環境の悪化が進展して行く
のに伴って、機器に使用されている材料は塩分濃度の高
い海浜の大気や排気ガス濃度の高い都市近郊の大気中で
使用される機会が多くなり、熱交換器の主要部で、材料
の腐食による機能の劣化が頻繁に認められる様になって
来た為、従来に増した耐腐食強度を有する材料の出現が
待たれる様になって来た。However, in recent years, as the areas in which the above devices are used have expanded and the environment in which they are used has become more and more deteriorating, the materials used in the devices have become increasingly salty. As heat exchangers are increasingly being used in the atmosphere on beaches and in the atmosphere near cities where exhaust gas concentration is high, deterioration of function due to material corrosion has become frequently observed in the main parts of heat exchangers. The emergence of materials with higher corrosion resistance than conventional materials has been awaited.
[発明が解決しようとする課題]
通常の黄銅は、価格的には手頃であるものの、腐食雰囲
気で応力のかけられた場合に発生して来る応力腐食割れ
現象には極めて敏感であり、特に、軽量を要求される熱
交換器用の材料としては、薄物化が要求される為、ます
ます腐食環境に耐えやすい素材の供給が望まれる様にな
って来て居る。[Problems to be Solved by the Invention] Although ordinary brass is reasonably priced, it is extremely sensitive to stress corrosion cracking phenomenon that occurs when stress is applied in a corrosive atmosphere. As materials for heat exchangers are required to be lightweight, they are required to be thin, so it is becoming more and more desirable to supply materials that can easily withstand corrosive environments.
本発明は、熱交換器用の素材に要求される性能を満足さ
せるものとして、熱伝導性や電気伝導性を低下させるこ
となく、素材価格もさほど高騰させずに、耐腐食性に優
れるという銅合金を提供する事を目的とするものである
。The present invention is a copper alloy that satisfies the performance required for materials for heat exchangers, and that has excellent corrosion resistance without reducing thermal conductivity or electrical conductivity, without significantly increasing the material price. The purpose is to provide the following.
[課題を解決するための手段]
本発明者等は、黄銅の脱亜鉛腐食性の改良を検討してい
る段階で、Cu−Zn合金にTeとPを含有させる事に
よって黄銅の脱亜鉛腐食性の著しい改良が認められる事
を見出だすと共に、更に、この合金の結晶粒度を調整す
る事によって、黄銅の耐腐食性を大幅に改善する事が可
能である事を見出だし、本発明に至ったものである。[Means for Solving the Problems] The inventors of the present invention were considering improving the dezincification corrosion resistance of brass by incorporating Te and P into a Cu-Zn alloy. The inventors have discovered that the corrosion resistance of brass can be significantly improved by adjusting the crystal grain size of this alloy, and have thus arrived at the present invention. It is something that
即ち、本発明は、重量%でZnを25〜38%と、Te
を0.005〜0.5%と、Pを0.005〜0.05
%含み、残部がCuおよび不可避不純物からなる黄銅で
あると共に、その平均結晶粒径が2〜10μmに調整さ
れた素材を利用する事によって、上記の課題を解決出来
る事を開示せんとしたものである。That is, in the present invention, Zn is 25 to 38% by weight and Te
0.005-0.5% and P 0.005-0.05
It is intended to disclose that the above-mentioned problems can be solved by using a material that is made of brass containing 1.5% of copper, with the remainder being Cu and unavoidable impurities, and whose average crystal grain size is adjusted to 2 to 10 μm. be.
[作用]
本発明に於いて、ZnはCuに固溶して材料強度を向上
させる機能を持たせる為のものであり、ここに、Znの
含有量を25〜38重量%と限定した理由は、Znの含
有量が25重量%未満では材料強度が十分でなくなると
共に、銅分が高くなる事から、価格の上昇を招く為であ
り、また、Znの含有量が38重量%を超えた場合には
β相の析出量が多量になり、材料の加工性が劣化して来
るためである。[Function] In the present invention, Zn is dissolved in Cu to give it the function of improving material strength, and the reason why the Zn content is limited to 25 to 38% by weight is as follows. If the Zn content is less than 25% by weight, the material strength will not be sufficient and the copper content will increase, leading to an increase in price.If the Zn content exceeds 38% by weight, This is because the amount of β phase precipitated becomes large and the workability of the material deteriorates.
次いで、Teは合金素地に固溶して黄銅の腐食形態を部
分的な脱亜鉛腐食から、全面的な腐食形態に移行させる
と共に、その腐食減量を軽減させる作用を為すものであ
るが、ここに、Teの含有量を0.005〜0.5重量
%と限定した理由は、Teの含有量が0.005重量%
未満では材料の脱亜鉛腐食を抑制する効果の向上が認め
られず、更に、Teの含有量が0.5重量%を超えて含
有される様になると、材料の全面腐食量が増加して来る
為、逆に腐食深さを軽減するという特性の向上効果が悪
化して来ると共に、Teが結晶粒界に析出してきて、材
料の加工性を損なう様になる為である。Next, Te acts as a solid solution in the alloy base to shift the corrosion form of brass from partial dezincification corrosion to full-scale corrosion, and to reduce the corrosion loss. , the reason why the content of Te is limited to 0.005 to 0.5% by weight is that the content of Te is 0.005% by weight.
If the Te content is less than 0.5% by weight, no improvement in the effect of suppressing dezincification corrosion of the material will be observed, and furthermore, if the Te content exceeds 0.5% by weight, the amount of general corrosion of the material will increase. This is because, on the contrary, the effect of improving the property of reducing the corrosion depth deteriorates, and Te precipitates at the grain boundaries, impairing the workability of the material.
また、Pは、材料の腐食形態を栓状から層状に変化させ
る効果があり、結果として、材料の腐食深さを減少させ
る事になる。Furthermore, P has the effect of changing the corrosion form of the material from plug-like to layer-like, resulting in a decrease in the corrosion depth of the material.
この場合、Pの含有量を0.005〜0.05重量%に
限定したのは、Pの含有量が0.005重量%未満では
材料の腐食形態を栓状から層状に変化させる効果が十分
で無く、逆に、Pの含有量が0.05重量%を超えた場
合には、結晶粒界にPが偏析してきて、結晶粒界部分が
優先的に腐食される様になり、かえって材料に悪影響を
及ぼす様になって来る為である。In this case, the reason why the P content is limited to 0.005 to 0.05% by weight is that a P content of less than 0.005% by weight is sufficient to change the corrosion form of the material from plug-like to layer-like. On the other hand, if the P content exceeds 0.05% by weight, P will segregate at the grain boundaries, and the grain boundaries will be preferentially corroded, causing the material to deteriorate. This is because it starts to have a negative impact on the
最後に、材料の結晶粒度を調整する事は、材料の深さ方
向に向かって展開していく腐食進行力を抑制する為に必
要なものであるが、この場合、材料の平均結晶粒径を2
〜10μmに調整するのは。Finally, adjusting the grain size of the material is necessary to suppress the corrosion progression force that develops in the depth direction of the material, but in this case, it is necessary to adjust the average grain size of the material. 2
It is adjusted to ~10 μm.
平均結晶粒径が2μm未満では加工組織が残存し易くな
り、かえって、材料の耐腐食性が悪化して来る為であり
、平均結晶粒径が10μmを超える場合には、材料の全
面腐食現象として認られる最大腐食深さを減少させる効
果が失われる様になって来る為である。If the average grain size is less than 2 μm, the processed structure tends to remain, and the corrosion resistance of the material deteriorates. If the average grain size exceeds 10 μm, it may cause general corrosion of the material. This is because the effect of reducing the maximum observed corrosion depth begins to be lost.
尚、材料の平均結晶粒径は、通常、最終焼鈍工程を終了
した状態で測定されるものであるが、ラジェーターのチ
ューブ材は、仕上げ工程に於ける圧延率が低い為、最終
の冷間圧延の前後に於いて平均結晶粒径に変化が認めら
れない事もあって、本明細書に於いて記述された平均結
晶粒径の値は、全て、最終冷間加工を終了した材料につ
いて測定されている。The average grain size of a material is normally measured after the final annealing process, but since the rolling rate of the radiator tube material is low in the finishing process, it is measured after the final cold rolling. Because no change is observed in the average grain size before and after the process, all values of the average grain size described in this specification are measured for the material that has undergone the final cold working. ing.
[実施例]
実施例1
電気銅3473gと、電気亜鉛1520gと、Cu−5
0%Te母合金1gと、Cu−15%P母合金5.9g
を原料とし、分析値としてZn30.4重量%と、Te
a、01重量%と、po。[Example] Example 1 3473 g of electrolytic copper, 1520 g of electrolytic zinc, and Cu-5
1g of 0% Te master alloy and 5.9g of Cu-15%P master alloy
was used as the raw material, and the analysis values were 30.4% by weight of Zn and Te.
a, 01% by weight, and po.
015重量%と、残部Cuとからなる銅合金を大気溶解
炉で溶製し、厚さ30mm、幅100mm長さ150m
mのインゴットを得た。A copper alloy consisting of 0.15% by weight and the balance Cu was melted in an atmospheric melting furnace to a thickness of 30 mm, width of 100 mm, and length of 150 m.
m ingots were obtained.
得られたインゴットは表面を片側2mmづつ面削りした
後、温度850°Cにて熱間圧延して厚さ10mmの中
間材とし、さらに、この中間材の表面を片側1mmづつ
面削した後、3 m mの厚さまで冷間圧延を施し、あ
らためて温度600°Cにて1時間の中間焼鈍を窒素雰
囲気中で行った。The surface of the obtained ingot was milled by 2 mm on each side, and then hot rolled at a temperature of 850°C to form an intermediate material with a thickness of 10 mm.Furthermore, the surface of this intermediate material was milled by 1 mm on each side, and then Cold rolling was performed to a thickness of 3 mm, and intermediate annealing was performed again at a temperature of 600°C for 1 hour in a nitrogen atmosphere.
中間焼鈍を施した材料について、引き続いて冷間圧延を
施して厚さ0.4mmの条材とした後、温度450°C
にて1時間にわたる最終焼鈍を窒素雰囲気中で行い、条
材の平均結晶粒径を5μmに調整した後、さらに、冷間
加工を施して厚さ03mmの条材とし、この条材から幅
25mm、長さ100mmの試験片を切り出し、結晶粒
度並びに耐腐食性の試験に供した。The material subjected to intermediate annealing was subsequently cold rolled into a strip with a thickness of 0.4 mm, and then rolled at a temperature of 450°C.
After final annealing for 1 hour in a nitrogen atmosphere to adjust the average grain size of the strip to 5 μm, cold working was performed to obtain a strip with a thickness of 0.3 mm, and from this strip, a width of 25 mm was obtained. A test piece with a length of 100 mm was cut out and subjected to grain size and corrosion resistance tests.
材料の結晶粒度を測定する場合には、JISH0501
に規定された伸銅品結晶粒度試験方法の比較法に従って
測定すると共に、材料の耐腐食性を調べる試験方法とし
ては、JIS Z2371に規定された塩水噴霧試験
方法を採用した。When measuring the grain size of materials, JISH0501
The measurement was carried out in accordance with the comparison method of the crystal grain size test method for rolled copper products specified in 1997, and the salt spray test method specified in JIS Z2371 was adopted as the test method for examining the corrosion resistance of the material.
この場合、試験片に対する塩水噴霧の処理時間は連続1
50時間とし、塩水噴霧処理の終了した試験片は幅方向
に6等分して切断された後、試験片の各切断面について
光学顕微鏡による腐食深さの測定を実施し、試験に供し
た幅25mmの試料の全長に亘っての計測を5箇所、都
合125mmについて行い、この間にあって、最も深く
腐食されている部分の深さをもって、その試料の最大腐
食深さとした。In this case, the treatment time of salt water spray on the test piece is 1 continuous time.
After the salt spray treatment was completed for 50 hours, the test piece was cut into 6 equal parts in the width direction, and the corrosion depth was measured using an optical microscope on each cut surface of the test piece. Measurements were taken over the entire length of the 25 mm sample at 5 locations, totaling 125 mm, and the depth of the most deeply corroded part between these points was defined as the maximum corrosion depth of the sample.
以上の様にして計測された試料の最大腐食深さは36μ
mであった。The maximum corrosion depth of the sample measured in the above manner was 36μ.
It was m.
実施例2
電気#i 3219 gと、電気亜鉛1770gと、5
0%Te−Cut合金2.5gと15%p−cU母合金
8.24gを原料とし、分析値としてZn35.4重量
%と、Tea、025重量%と、Po、021重量%と
、残部Cuとからなる銅合金を得、平均結晶粒径を4μ
mとした以外は、実施例1と同様な方法にて処理された
結果、計測された試料の最大腐食深さは38μmであっ
た。Example 2 Electric #i 3219 g, electrolytic zinc 1770 g, 5
Using 2.5 g of 0% Te-Cut alloy and 8.24 g of 15% p-cU master alloy as raw materials, the analysis values were 35.4% by weight of Zn, 025% by weight of Tea, 021% by weight of Po, and the balance Cu. A copper alloy with an average crystal grain size of 4μ was obtained.
As a result of processing in the same manner as in Example 1 except that m was used, the measured maximum corrosion depth of the sample was 38 μm.
実施例3
電気銅3221gと、電気亜鉛1735gと、50%T
e−Cu母合金38gと、15%P−CU母合金5.9
gとを原料とし、分析値としてZn34.7重量%と、
Tea、38重量%と5PO,021重量%、残部Cu
とからなる銅合金を得、その平均結晶粒径を5μmとし
た以外は、実施例1と同様な方法にて処理された結果、
計測された試料の最大腐食深さは36μmであった。Example 3 3221 g of electrolytic copper, 1735 g of electrolytic zinc, and 50% T
38g of e-Cu master alloy and 5.9g of 15% P-CU master alloy
g is used as a raw material, and the analysis value is 34.7% by weight of Zn,
Tea, 38% by weight and 5PO, 021% by weight, balance Cu
As a result of processing in the same manner as in Example 1, except that the average crystal grain size was 5 μm, a copper alloy consisting of
The measured maximum corrosion depth of the sample was 36 μm.
比較例1
平均結晶粒径が5μmに調整されたZn含有量30.3
重量%の黄銅を試料とした以外は、実施例1と同様な方
法にて処理された結果、計測された試料の最大腐食深さ
は82μmであった。Comparative Example 1 Zn content 30.3 with average crystal grain size adjusted to 5 μm
As a result of processing in the same manner as in Example 1 except that the sample was made of brass having a weight of %, the measured maximum corrosion depth of the sample was 82 μm.
比較例2 分析値としてZn35.5重量%と、Tea。Comparative example 2 The analysis values were 35.5% by weight of Zn and Tea.
003重量%と、Po、030重量%と、残部CUとか
らなる銅合金を得、その平均結晶粒径を7μmとした以
外は、実施例1と同様な方法にて処理された結果、計測
された試料の最大腐食深さは51μmであった。A copper alloy consisting of 003% by weight, Po, 030% by weight, and the balance CU was obtained, and as a result of processing in the same manner as in Example 1, except that the average crystal grain size was 7 μm, the results were measured. The maximum corrosion depth of the sample was 51 μm.
比較例3
分析値としてZn35.4重量%と、20102重量%
と、残部Cuとからなる銅合金を得、その平均結晶粒径
を6μmとした以外は、実施例1と同様な方法にて処理
された結果、計測された試料の最大腐食深さは56μm
であった。Comparative Example 3 Analysis values: Zn 35.4% by weight and 20102% by weight
A copper alloy consisting of , and the remainder Cu was obtained, and treated in the same manner as in Example 1, except that the average grain size was 6 μm. As a result, the maximum corrosion depth of the measured sample was 56 μm.
Met.
比較例4 分析値としてZn34.7重量%と、T e 0 。Comparative example 4 The analysis values were Zn 34.7% by weight and T e 0.
032重量%と、Po、054重量%と、残部CUとか
らなる銅合金を得、その平均結晶粒径を5μmとした以
外は、実施例1と同様な方法にて処理された結果、計測
された試料の最大腐食深さは54μmであった。A copper alloy consisting of 032% by weight, Po, 054% by weight, and the balance CU was obtained, and as a result of processing in the same manner as in Example 1, except that the average crystal grain size was 5 μm, the results were measured. The maximum corrosion depth of the sample was 54 μm.
比較Fs5 分析値としてZn35.1重量%と、Tea。Comparison Fs5 The analysis values were 35.1% by weight of Zn and Tea.
03重量%と、Po、022重量%と、残部Cuとから
なる銅合金を得、その平均結晶粒径を20μmとした以
外は、実施例1と同様な方法にて処理された結果、計測
された試料の最大腐食深さは45μmであった。A copper alloy consisting of 0.3% by weight, Po, 0.22% by weight, and the balance Cu was obtained, and as a result of processing in the same manner as in Example 1, except that the average crystal grain size was 20 μm, the results were measured. The maximum corrosion depth of the sample was 45 μm.
以上の如く、本発明の実施による場合には、腐食環境に
あっても、高度な耐食性が示される素材を容易に入手す
る事が可能になった。As described above, by carrying out the present invention, it has become possible to easily obtain a material that exhibits a high degree of corrosion resistance even in a corrosive environment.
以上の計測結果を第1表として示す。The above measurement results are shown in Table 1.
又、平均結晶粒径を変化させた同一組成の合金について
、材料の最大腐食深さを測定した結果を纏めて第2表に
示す。Further, Table 2 summarizes the results of measuring the maximum corrosion depth of materials for alloys of the same composition with different average grain sizes.
(この頁以下余白)
[発明の効果]
本発明の実施により、復水器、加水加熱器、蒸留器、冷
却器、遣水装置等の熱交換器用の材料として、特に、自
動車等に用いられるラジェーターのチューブ材として好
適な、耐腐食性に優れた黄銅を容易に入手する事を可能
にした為、斯業界に寄与するところ大なるものがある。(Margins below this page) [Effects of the invention] By carrying out the present invention, radiators used in automobiles, etc. can be used as materials for heat exchangers such as condensers, water heaters, distillers, coolers, water supply devices, etc. It has made it possible to easily obtain brass, which has excellent corrosion resistance and is suitable as a tube material, making a great contribution to this industry.
Claims (1)
〜0.5%と、Pを0.005〜0.05%含み、残部
がCuおよび不可避不純物からなる事を特徴とするTe
とPが添加された耐腐食性に優れる黄銅。 2)平均結晶粒径が2〜10μmである事を特徴とする
請求項1記載のTeとPが添加された耐腐食性に優れる
黄銅。[Claims] 1) 25 to 38% Zn and 0.005% Te by weight;
~0.5% and 0.005 to 0.05% of P, with the remainder consisting of Cu and inevitable impurities.
Brass with excellent corrosion resistance and P added. 2) The brass with excellent corrosion resistance to which Te and P are added according to claim 1, characterized in that the average crystal grain size is 2 to 10 μm.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP24953290A JPH04128333A (en) | 1990-09-18 | 1990-09-18 | Te-and p-added brass excellent in corrosion |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP24953290A JPH04128333A (en) | 1990-09-18 | 1990-09-18 | Te-and p-added brass excellent in corrosion |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH04128333A true JPH04128333A (en) | 1992-04-28 |
Family
ID=17194386
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP24953290A Pending JPH04128333A (en) | 1990-09-18 | 1990-09-18 | Te-and p-added brass excellent in corrosion |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH04128333A (en) |
-
1990
- 1990-09-18 JP JP24953290A patent/JPH04128333A/en active Pending
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