JPH04128332A - Te-added brass excellent in corrosion resistance - Google Patents
Te-added brass excellent in corrosion resistanceInfo
- Publication number
- JPH04128332A JPH04128332A JP24953190A JP24953190A JPH04128332A JP H04128332 A JPH04128332 A JP H04128332A JP 24953190 A JP24953190 A JP 24953190A JP 24953190 A JP24953190 A JP 24953190A JP H04128332 A JPH04128332 A JP H04128332A
- Authority
- JP
- Japan
- Prior art keywords
- weight
- grain size
- corrosion resistance
- corrosion
- brass
- 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
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
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
て入手出来る事がら、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1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 deteriorated, the materials used in the devices have a high salt concentration. 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, while considering improving the dezincification corrosivity of brass, found that by incorporating Te into a Cu-Zn alloy, the dezincification corrosivity of brass was significantly improved. In addition to discovering that improvements can be observed, they also discovered that by adjusting the crystal grain size of this alloy, it is possible to significantly improve the corrosion resistance of brass, leading to the present invention. It is.
即ち、本発明は、重量%でZnを25〜38%と、Te
を0.005〜0.5%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
Brass contains 0.005 to 0.5% of CU and the remainder is CU and unavoidable impurities, and its average crystal grain size is 2.
It is intended to disclose that the above-mentioned problems can be solved by using a material whose thickness is adjusted to ~10 μm.
[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、績な、2n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. In this case, 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ν)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. Therefore, if the corrosion depth is reduced, the effect of improving the properties of
This is because the workability of the material will be impaired.
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 crystal 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33524と、電気亜鉛1475gと、Cu−5
0%Te母合金1.1gとを原料とし、分析値としてZ
n29.5重量%と、Te0.01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30 m
m 、輻100mm、長さ150mmのインゴットを
得た。[Example] Example 1 Electrolytic copper 33524, electrolytic zinc 1475g, Cu-5
Using 1.1 g of 0% Te master alloy as raw material, the analysis value is Z
n29.5% by weight, Te0.01% by weight, balance Cu
A copper alloy consisting of
An ingot with a radius of 100 mm and a length of 150 mm was obtained.
得られたインゴットは表面を片側2mmづつ面側りした
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
面側した後+ 3mm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 chamfered 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 chamfered by 1 mm on each side. After cold rolling to a thickness of +3 mm, 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6μmに調整した後、さらに、冷間
加工を施して厚さ0゜3mm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 6 μm, it was further cold-worked into a strip with a thickness of 0.3 mm. A test piece with a width of 25 mm and 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
方法を採用しな。When measuring the grain size of materials, JISH0501
In addition to measuring according to the comparison method of the crystal grain size test method for rolled copper products specified in 2013, the salt spray test method specified in JIS Z2371 is used as the test method to check 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39μ
mであった。The maximum corrosion depth of the sample measured as above was 39μ.
It was m.
実施例2
電気銅3227gと、電気亜鉛1765gと、50%T
e−Cu母合金8gとを原料とし、分析値としてZn3
5−3重量%と、Tea、08重量%と、残部Cuとか
らなる銅合金を得、平均結晶粒径を8μm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32μmであった。Example 2 3227 g of electrolytic copper, 1765 g of electrolytic zinc, and 50% T
Using 8g of e-Cu master alloy as raw material, the analysis value is Zn3
A copper alloy consisting of 5-3% by weight, Tea, 08% by weight, and the balance Cu was obtained and treated in the same manner as in Example 1 except that the average crystal grain size was 8 μm. As a result, the results were measured. The maximum corrosion depth of the sample was 32 μm.
実施例3
電気銅3227gと、電気亜鉛1740gと、50%T
e −Cu母合金33gとを原料とし、分析値として
Zn34.8重量%と、Tea、33重量%と、残部C
uとからなる銅合金を得、その平均結晶粒径を4μm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35μmであった。Example 3 3227 g of electrolytic copper, 1740 g of electrolytic zinc, and 50% T
Using 33g of e-Cu master alloy as a raw material, the analysis values were 34.8% by weight of Zn, 33% by weight of Tea, and the balance C.
A copper alloy consisting of u was obtained, and the sample was treated in the same manner as in Example 1, except that the average crystal grain size was 4 μm. As a result, the maximum corrosion depth of the measured sample was 35 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、Te01003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75
μmであった。Comparative Example 2 A copper alloy consisting of 35.5% by weight of Zn, 3% by weight of Te, and the balance Cu was obtained as an analysis value, and treated in the same manner as in Example 1 except that the average crystal grain size was 7 μm. As a result, the maximum corrosion depth of the sample measured was 75
It was μm.
比較例3 分析値としてZn35.4重量%と、Tea。Comparative example 3 The analysis values were 35.4% by weight of Zn and Tea.
10重量%と、Po、02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。A copper alloy consisting of 10% by weight, Po, 02% by weight, and the balance Cu was obtained, and the result was measured in the same manner as in Example 1, except that the average crystal grain size was 6 μm. The maximum corrosion depth of the sample was 56 μm.
比較例4 分析値としてZn35.3重量%と、Tea。Comparative example 4 The analysis values were 35.3% by weight of Zn and Tea.
08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42μmであった。A copper alloy consisting of 0.8% by weight and the balance Cu was obtained, and the treatment was carried out in the same manner as in Example 1, except that the average grain size was 20 μm. As a result, the maximum corrosion depth of the measured sample was was 42 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%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;
Te-added brass with excellent corrosion resistance characterized by containing ~0.5% of Te with the remainder consisting of Cu and unavoidable impurities. 2) The Te-added brass with excellent corrosion resistance 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 |
|---|---|---|---|
| JP24953190A JPH04128332A (en) | 1990-09-18 | 1990-09-18 | Te-added brass excellent in corrosion resistance |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP24953190A JPH04128332A (en) | 1990-09-18 | 1990-09-18 | Te-added brass excellent in corrosion resistance |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH04128332A true JPH04128332A (en) | 1992-04-28 |
Family
ID=17194369
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP24953190A Pending JPH04128332A (en) | 1990-09-18 | 1990-09-18 | Te-added brass excellent in corrosion resistance |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH04128332A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2406406A4 (en) * | 2009-03-09 | 2015-09-02 | Nat Bronze & Metals Inc | BRASS ALLOY WITHOUT LEAD |
-
1990
- 1990-09-18 JP JP24953190A patent/JPH04128332A/en active Pending
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2406406A4 (en) * | 2009-03-09 | 2015-09-02 | Nat Bronze & Metals Inc | BRASS ALLOY WITHOUT LEAD |
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