JPS6328717B2 - - Google Patents
Info
- Publication number
- JPS6328717B2 JPS6328717B2 JP56110756A JP11075681A JPS6328717B2 JP S6328717 B2 JPS6328717 B2 JP S6328717B2 JP 56110756 A JP56110756 A JP 56110756A JP 11075681 A JP11075681 A JP 11075681A JP S6328717 B2 JPS6328717 B2 JP S6328717B2
- Authority
- JP
- Japan
- Prior art keywords
- copper
- zinc
- brazing
- phosphorus
- brazing filler
- 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
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 14
- 229910052802 copper Inorganic materials 0.000 claims description 14
- 239000010949 copper Substances 0.000 claims description 14
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 11
- 239000011701 zinc Substances 0.000 claims description 11
- 229910052725 zinc Inorganic materials 0.000 claims description 11
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 9
- 229910052698 phosphorus Inorganic materials 0.000 claims description 9
- 239000011574 phosphorus Substances 0.000 claims description 9
- 239000010936 titanium Substances 0.000 claims description 8
- 229910052719 titanium Inorganic materials 0.000 claims description 8
- 229910000679 solder Inorganic materials 0.000 claims description 6
- 229910052726 zirconium Inorganic materials 0.000 claims description 6
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 4
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims description 4
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 claims description 3
- 239000000203 mixture Substances 0.000 claims description 2
- 238000005219 brazing Methods 0.000 description 16
- 239000000463 material Substances 0.000 description 8
- 239000000945 filler Substances 0.000 description 7
- 229910052751 metal Inorganic materials 0.000 description 7
- 239000002184 metal Substances 0.000 description 7
- 238000002844 melting Methods 0.000 description 5
- 230000008018 melting Effects 0.000 description 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 229910052717 sulfur Inorganic materials 0.000 description 4
- 239000011593 sulfur Substances 0.000 description 4
- RIRXDDRGHVUXNJ-UHFFFAOYSA-N [Cu].[P] Chemical compound [Cu].[P] RIRXDDRGHVUXNJ-UHFFFAOYSA-N 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- 229910000881 Cu alloy Inorganic materials 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000005486 sulfidation Methods 0.000 description 2
- 229910017888 Cu—P Inorganic materials 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000010953 base metal Substances 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000004907 flux Effects 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 238000005476 soldering Methods 0.000 description 1
- 238000009864 tensile test 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
- B23K35/30—Selection of soldering or welding materials proper with the principal constituent melting at less than 1550 degrees C
- B23K35/302—Cu as the principal constituent
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Electric Connection Of Electric Components To Printed Circuits (AREA)
- Ceramic Products (AREA)
Description
〔産業上の利用分野〕
本発明はイオウを含む硫化雰囲気で使用される
銅及び銅合金用りん銅ろうに関するものである。
〔従来技術〕
銅及び銅合金の硬ろう付用ろう材としてのりん
銅ろうは安価であるので広く使用されている。と
ころがこのりん銅ろうでろう付けしたものをイオ
ウを含む硫化系雰囲気中で使用すると母材との境
界部が著しく腐食されろう付け部が剥離してろう
材としての役目を果さなくなる。
そこで本発明者等は先に重量%でりん1〜9
%、亜鉛0.5〜45%、銅52〜83.5%からなる耐硫
化性の優れたりん銅ろう(特開昭57―44491号公
報参照)を発明した。
このろう材は亜鉛を0.5%以上入れると耐硫化
性が良くなるが50%以上ではγ相の析出により脆
くなる。さらにろう付け性から融点を850℃以下
にするためにりんを1〜9%入れており、それに
伴つてγ相の析出が亜鉛45%以上で起ることから
組成範囲を決めている。
〔発明が解決しようとする問題点〕
ところが、このりん銅ろうをある程度拘束され
た母材、例えばかご形誘導電動機の回転子におけ
るロータバーとエンドリングとの接合に使用する
ような場合にろう付後、ろう材中の冷却収縮によ
る微小亀裂を生じろう付部の接着強度が低下する
欠点があることが分つた。
本発明は、この欠点を改善するためになされた
ものである。
〔問題点を解決するための手段〕
本発明は、上記の問題点を解決するためりん1
〜9%、亜鉛0.5〜45%、銅52〜83.5%の組成の
りん銅ろうに、チタンとジルコニウムの何れか一
方または双方を0.05〜1.5%の範囲で混ぜて微小
亀裂を防止したものである。
上記各成分量の下限及び上限を定めた理由は次
の通りである。
即ち、リンが1%未満であれば融点が上り、9
%を越えると脆くなる。また亜鉛が45%を越える
とγ相の析出量が多くなつて脆くなり、0.5%未
満であれば融点が高くろう材としては使い勝手が
悪い。更にTi,Zr又はTi+Zrが1.5%を越える
と、多くの巣の発生が観察され、強度が低下し、
0.05%未満では結晶の微細化効果が生じないた
め、上記のように定めたものである。
なお、銅については他の成分量との関係から定
めたものである。
〔作用〕
銅にりんや亜鉛を添加したろう材はろう付け時
に液体から固体になる前に固体結晶中に少量の液
体を含む状態が存在する。この状態で外力が加わ
る(つまりろう付部が拘束されている)と液体の
部分から割れを生じる。チタンやジルコニウムを
添加すると液体の存在する個所が増え(結晶粒の
微細化)、応力の分散を計ることができるので、
微細亀裂が発生しなくなる。
〔実施例〕
以下、本発明の実施例について説明する。
第1表に示すように重量%で、りん1〜9%、
亜鉛0.5〜45%、銅52〜83.5%よりなるろう材に
更にチタンおよびジルコニウムを単独又は同時に
添加した20種類のろう材を溶製した。なお比較の
ため、第1表に示すような重量%でりん1〜9
%、亜鉛0.5〜45%残部銅の組成からなる4種類
のろう材を溶製した。
そして各ろう材を使用して、0.3mmの継手間隙
をとつた状態で固定した2本の10mmの銅丸棒をろ
う付けし、各試験片の引張り試験を行なつた。そ
の結果は第1表の通りである。
ろう付けの手順としては、母材をろう材の融点
直上50〜100℃にバーナーで予熱したあと、ろう
付けを行つた。ろう材中に亜鉛を1%以上含むも
のについてはフラツクス(ホウ砂+ホウ酸)を使
用した。
[Industrial Application Field] The present invention relates to a phosphorous copper solder for copper and copper alloys used in a sulfur-containing sulfur atmosphere. [Prior Art] Phosphorus copper solder is widely used as a brazing material for hard soldering of copper and copper alloys because it is inexpensive. However, when a product brazed with phosphor copper braze is used in a sulfur-based atmosphere containing sulfur, the interface with the base material is severely corroded, the brazed part peels off, and it no longer functions as a brazing material. Therefore, the present inventors first determined that phosphorus was 1 to 9% by weight.
%, zinc 0.5 to 45%, and copper 52 to 83.5%, and has excellent sulfidation resistance (see Japanese Patent Laid-Open No. 44491/1983). This brazing filler metal will have better sulfidation resistance if it contains 0.5% or more zinc, but if it contains more than 50% it becomes brittle due to the precipitation of the γ phase. Furthermore, phosphorus is added in an amount of 1 to 9% in order to lower the melting point to 850° C. or less for brazing properties, and the composition range is determined based on the fact that γ phase precipitation occurs at 45% or more zinc. [Problems to be Solved by the Invention] However, when this phosphor copper solder is used to join a base material that is constrained to some extent, for example, a rotor bar and an end ring in a rotor of a squirrel-cage induction motor, It has been found that this method has the disadvantage that micro-cracks occur due to cooling shrinkage in the brazing filler metal, resulting in a decrease in the adhesive strength of the brazed portion. The present invention has been made to improve this drawback. [Means for solving the problems] In order to solve the above problems, the present invention provides phosphorus 1
~9% zinc, 0.5~45% zinc, and 52~83.5% copper, mixed with titanium and/or zirconium in the range of 0.05~1.5% to prevent microcracks. . The reason for determining the lower and upper limits of the amounts of each of the above components is as follows. That is, if the phosphorus content is less than 1%, the melting point increases, and 9
If it exceeds %, it becomes brittle. Moreover, if the zinc content exceeds 45%, the amount of γ phase precipitated increases and becomes brittle, while if it is less than 0.5%, the melting point is high and it is not convenient to use as a brazing material. Furthermore, when Ti, Zr or Ti+Zr exceeds 1.5%, many nests are observed, the strength decreases,
If the content is less than 0.05%, the crystal refinement effect will not occur, so it is determined as above. Note that copper is determined based on the relationship with the amounts of other components. [Operation] A brazing material made of copper with phosphorus or zinc added contains a small amount of liquid in its solid crystals before it changes from liquid to solid during brazing. If an external force is applied in this state (that is, the brazed part is restrained), cracks will occur from the liquid part. Adding titanium or zirconium increases the number of locations where liquid exists (refining crystal grains), which allows for stress dispersion.
Microcracks will no longer occur. [Examples] Examples of the present invention will be described below. As shown in Table 1, phosphorus 1 to 9% by weight,
Twenty types of brazing filler metals were produced by adding titanium and zirconium either singly or simultaneously to a brazing filler metal consisting of 0.5 to 45% zinc and 52 to 83.5% copper. For comparison, phosphorus 1 to 9 in weight% as shown in Table 1
%, zinc, and 0.5 to 45% copper as the balance. Then, each brazing filler metal was used to braze two 10 mm round copper rods fixed together with a 0.3 mm joint gap, and a tensile test was conducted on each test piece. The results are shown in Table 1. The brazing procedure involved preheating the base metal with a burner to 50 to 100°C, just above the melting point of the brazing material, and then brazing. For brazing filler metals containing 1% or more of zinc, flux (borax + boric acid) was used.
【表】【table】
以上述べたように、本発明によるりん銅ろう
は、母材が拘束されていても、微小クラツクの発
生がなく、作業性良く、しかも低価格で提供し得
るという特長がある。
なおCu―P系ろう材にAgを添加すると、加工
性が良くなり、強度が向上すること、またSnを
添加すると融点が下ることは公知であるが、必要
に応じてこれら金属を本発明にかゝるりん銅ろう
に添加すれば、更に応用範囲も拡大することがで
きる。
As described above, the phosphorous copper solder according to the present invention has the advantage that even if the base material is restrained, it does not generate microcracks, has good workability, and can be provided at a low price. It is known that adding Ag to Cu-P brazing filler metal improves workability and strength, and that adding Sn lowers the melting point. If phosphorus is added to copper solder, the range of applications can be further expanded.
第1図は本発明実施例におけるTi,Zr,Ti+
Zrの添加量と引張り強さの関係を示すグラフで
ある。
Figure 1 shows Ti, Zr, Ti+ in the embodiment of the present invention.
It is a graph showing the relationship between the amount of Zr added and tensile strength.
Claims (1)
52〜83.5%およびチタンとジルコニウムの何れか
一方または双方を0.05〜1.5%の組成より成るり
ん銅ろう。1% by weight phosphorus 1-9%, zinc 0.5-45%, copper
A phosphorous copper solder having a composition of 52 to 83.5% and 0.05 to 1.5% of titanium and/or zirconium.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11075681A JPS5813492A (en) | 1981-07-17 | 1981-07-17 | Phosphor copper solder |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11075681A JPS5813492A (en) | 1981-07-17 | 1981-07-17 | Phosphor copper solder |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5813492A JPS5813492A (en) | 1983-01-25 |
JPS6328717B2 true JPS6328717B2 (en) | 1988-06-09 |
Family
ID=14543763
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP11075681A Granted JPS5813492A (en) | 1981-07-17 | 1981-07-17 | Phosphor copper solder |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5813492A (en) |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS50145347A (en) * | 1974-05-14 | 1975-11-21 | ||
JPS5476462A (en) * | 1977-11-30 | 1979-06-19 | Yaskawa Denki Seisakusho Kk | Silver solder |
-
1981
- 1981-07-17 JP JP11075681A patent/JPS5813492A/en active Granted
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS50145347A (en) * | 1974-05-14 | 1975-11-21 | ||
JPS5476462A (en) * | 1977-11-30 | 1979-06-19 | Yaskawa Denki Seisakusho Kk | Silver solder |
Also Published As
Publication number | Publication date |
---|---|
JPS5813492A (en) | 1983-01-25 |
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