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JPH0524981B2 - - Google Patents
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JPH0524981B2 - - Google Patents

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Publication number
JPH0524981B2
JPH0524981B2 JP61070382A JP7038286A JPH0524981B2 JP H0524981 B2 JPH0524981 B2 JP H0524981B2 JP 61070382 A JP61070382 A JP 61070382A JP 7038286 A JP7038286 A JP 7038286A JP H0524981 B2 JPH0524981 B2 JP H0524981B2
Authority
JP
Japan
Prior art keywords
present
phase
bonding
superplasticity
solid phase
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 - Fee Related
Application number
JP61070382A
Other languages
Japanese (ja)
Other versions
JPS62227598A (en
Inventor
Yasuhiro Maehara
Toshiro Tomita
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nippon Steel Corp
Original Assignee
Sumitomo Metal Industries Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Sumitomo Metal Industries Ltd filed Critical Sumitomo Metal Industries Ltd
Priority to JP7038286A priority Critical patent/JPS62227598A/en
Publication of JPS62227598A publication Critical patent/JPS62227598A/en
Publication of JPH0524981B2 publication Critical patent/JPH0524981B2/ja
Granted legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B23MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
    • B23KSOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
    • B23K35/00Rods, electrodes, materials, or media, for use in soldering, welding, or cutting
    • B23K35/22Rods, electrodes, materials, or media, for use in soldering, welding, or cutting characterised by the composition or nature of the material
    • B23K35/24Selection of soldering or welding materials proper
    • B23K35/30Selection of soldering or welding materials proper with the principal constituent melting at less than 1550°C
    • B23K35/3053Fe as the principal constituent
    • B23K35/308Fe as the principal constituent with Cr as next major constituent
    • B23K35/3086Fe as the principal constituent with Cr as next major constituent containing Ni or Mn

Landscapes

  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Pressure Welding/Diffusion-Bonding (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

(産業上の利用分野) 本発明は、Fe基合金を用いた接合用薄帯に関
する。 (従来の技術) 超塑性材料を使つた固相接合についてはすでに
良く知られている〔例えば、(「超塑性と金属加工
技術」:超塑性研究会編(1980)、日刊工業新聞
社、p.151)参照〕。 しかしながら、一般に、超塑性材料は通常の加
工においては難加工性を示すものが多いので、そ
の薄帯をサンドイツチにはさんだ固相接合のアイ
デアはあつても(特開昭52−45567号)その実用
化は困難であつた。固相接合の場合、厚さ数mm以
下の薄帯に成形しなければならず、工業的なコス
トで従来公知の超塑性材料をそのように加工する
ことはできなかつた。 (発明が解決しようとする問題点) 本発明の目的は、上述のような従来技術の諸欠
点を解消した、超塑性を示す固相接合用Fe基合
金薄帯を提供することである。 (問題点を解決するための手段) かくして、本発明者は固相接合用の材料につい
て種々検討を重ねたところ、2相ステンレス鋼で
超塑性を示すものが、特にすぐれていることを知
り、さらに研究を重ね、その合金組成を特定化す
るとともに、加工性に難点がある場合には、好ま
しくは、溶湯からの直接の成形によつて薄帯とす
ることで、超塑性化とともに成形が行われること
を知り、本発明を完成した。 ここに、本発明の要旨とするところは、重量
%、Si≧0.5%、およびMn≧1.7%の1種または
2種を含有し、かつ Si eq=Si+2/3(Cr+Mo)およびMn eq=
Mn+2Ni+60C+50Nで規定されるSi eqおよび
Mn eqが次式の関係を満足し、 5/6Si eq−15/2≦Mn eq≦11/5Si eq−77/5 残部実質的にFeからなる合金組成を有する、
固租接合用Fe基合金薄帯である。 さらにまた、本発明は、好ましくは、急冷凝固
によつて超塑性に優れた薄帯を溶湯から直接に製
造し、その超塑性を利用した優れた肉流れによる
密着性に基づく極めて短い拡散距離を利用した拡
散接合方法を実現可能とするもので、その接合、
対象材料は特に制限されないが鉄合金がより好ま
しい。 また、上述のような急冷凝固によれば厚さ2mm
以下の薄帯が加工性を問題とすることなく容易に
製造できる。 (作用) 次に、本発明において、合金組成を上述のよう
に限定した理由を述べる。 まず、上述のように限定されたSi eqおよび
Mn eqは700〜1200℃という熱間加工条件下で
α/(α+γ)の比が0.2〜0.8となる範囲を規定
するものであつて、そのような条件を満足する限
り、個々の具体的組成に係わらずα/(α+γ)
=0.2〜0.8が満足され、超塑性が実現される。好
ましくは、1.1Si eq−10.8≦Mn eq≦1.7Si eq−
14であつて、Si eq=10〜20である。この好まし
いSi eqおよびMn eqの範囲は後述する第1図に
斜線で示した範囲であるが、これは超塑性変形中
のα相とγ相の相比が約1:1となつたものがよ
り好ましいということであり、これは製品の性質
の確保の上からも好ましい。 第1図は、Mn eqとSi eqとの間の上述の関係
をまとめて示すグラフである。 Si eqおよびMn eqをまず上述のように定義し
たのは、すでに述べたところからも明らかなよう
に、それぞれフエライト生成元素のSi換算当量、
およびオーステナイト生成元素のMn換算当量を
得るためである。本発明の場合、SiおよびMnに
より2相組織を調整するためそれぞれについて上
述のように定義するのである。 また、それらを上述の範囲に限定したのは、そ
の範囲でα相とγ相との2相組織となり、熱間加
工時のγ相の割合が0.2〜0.8となつて優れた超塑
性が得られるからである。 また、0.5%以上のSiもしくは1.7%以上のMn
のいずれかを含有することを条件としたのは本発
明の目的が必ずしも耐食性を必要とせず安価な超
塑性用Fe基合金を提供しようとするものであり、
SiもしくはMnを積極的に利用しようとするから
であり、従来脱酸材として使用されていた量以上
のものを本発明においては添加するのである。 本発明においてSiおよびMnの上限は特に限定
されるものではないが、第3元素をFeとして考
えた場合、所望の2相組織を得るには、Si<10
%、Mn<15%とすることにより組織調整がより
容易となる。 したがつて、本発明の一つの好適態様によれ
ば、その合金組成は、Si:0.5〜10重量%、およ
び/またはMn:1.7〜15%、残部Feである。 また、本発明の上述のような2相組織を得ると
いう趣旨からは、Ni、CrあるいはMoの添加量は
制限されないが、経済的理由からは、それぞれ
Ni:0〜5%、Cr:0〜20%、Mo:0〜2.5%
に制限される。もし、耐食性を確保したいなら
ば、必要に応じてCrやMoを増量すればよい。 したがつて、本発明の別の態様によれば、その
合金組成は、Si:0.5〜10重量%、および/また
はMn:1.7〜15重量%、ならびにNi:5重量%
以下、Cr:20重量%以下およびMo:2.5重量%以
下の少なくとも1種、残部Feと不可避不純物か
ら成るのもである。 本発明にかかる2相合金には、Fe、Si、Cr、
Mo、NやCのほかに、必要に応じて、Cu≦1.0
%、Ti≦0.5%、Zr≦0.5%、Nb≦0.5%、V≦0.5
%、W≦1.0%のうち少なくとも1種以上を含有
したものや、さらにその他、少量のRe、Ca、Ce
や不可避不純物を含むものも本発明に包含され
る。 しかしながら、Ti、Zr、Nb、Vは窒化物を容
易に生成して超塑性に有効な固溶N量を低減させ
るので、できれば添加しないほうがよい。 Cは炭化物を生成して製品の性質を害すること
もあるので、低いほうが好ましい。 Nは有力なγ生成元素であり、MnやNiに比べ
て拡散しやすく、したがつて、熱活性化過程によ
る組織変化を助けて超塑性変形を発現しやすく
し、しかも最も安価であることから、できるだけ
多量に、好ましくは、0.01〜0.25%程度含有させ
るのが有利となる。 以上のように、本発明にあつてはα+γ型2相
組織を呈する限りにおいてそのすぐれた超塑性現
象を利用できるのであつて、上述の各種添加元素
およびその添加量を変えても、前述の第1図に示
す条件を満足する限り、実質上α+γ型2相組織
は何ら変更を受けないことが確認されている。 本発明にかかる薄帯の製造方法は特に問わない
が、一般に2相系合金が難加工材であることを考
えると急冷凝固によるのが好ましく、通常の片ロ
ール、双ロールもしくは、その他の方法が適用で
きる。冷却速度は特に限定されないが、組織が微
細になつたほうが、後の超塑性変形能を向上させ
るため100℃/sec以上が好ましい。より好ましく
は103℃/sec以上である。 また、上記薄帯の厚さは、薄いほうが冷却速度
を上げられ、かつ接合上効率的であるので、好ま
しくは、その上限は2mmとする。下限は、特にな
いが急冷薄帯製造上の理由により20μmとなる。 このようにして得られた薄帯はそのまま固相接
合に利用することも可能であるが、板表面性状の
改善およびさらに後工程で組織を微細にするた
め、熱間加工もしくは冷却加工等を施しても良
い。これらの処理は固相接合時に再結晶によつて
組織を著しく微細化し、超塑性を向上させるが、
それには各々、50%、20%以上が好ましい。熱間
圧延の温度は、上記目的を達成するために、低い
ほうが好ましく1200℃以下、より好ましくは1000
℃以下で行うのが良い。 本発明により得られた固相接合用薄帯を使つて
固相接合する場合、その具体的条件は特に限定さ
れないが、好ましくは、まず接合面を清浄面とし
から750〜1200℃に加熱し、0.5Kgf/mm2以上の加
圧力をかけながら接合を行えばよい。 温度を750〜1200℃に限定する理由は、この範
囲で2相ステンレス鋼の超塑性が得やすいからで
あり、かつ固相接合素材の組織が粗くなつたりせ
ず、本来の性質を損なわないからである。より好
ましくは900〜1100℃とするのがよい。 加熱は、どのような方法であつても良いが、ス
ケール防止のため、2相系ステンレス鋼中に多量
に含有される窒素を多く含有するN2ガス雰囲気
中で加熱することが好ましい。 接合のための圧縮力は0.5Kgf/mm2上が必要で
あり、あまり大きすぎると座屈、変形が大きくな
るため、10Kgf/mm2以下にとどめるのが望まし
い。 加熱、加圧により接合された2相系ステンレス
鋼は、そのまま冷却されるが、冷却中にシグマ相
が生成すると著しく靭性を害するため、5℃/
min以上の冷却速度で冷却し、できれば1000〜
1200℃近傍に加熱後急冷すれば溶体化処理を施し
たのと実質的に同じとなるため好ましい。 接合に供する素材としては特に限定されない
が、拡散接合性が良く異種元素間の拡散係数の著
しい差によつて生じるカーケンダルボイドや機械
的性質を劣化させる金属間化合物からなる中間相
等を生じにくい鉄基合金が好ましく、低合金鋼、
オーステナイト系、フエライト系ステンレス鋼が
適用でき、Ni基合金にも適用が可能である。 次に、実施例によつて本発明をさらに詳述する
が、それらは単に本発明の例として示すもので、
それによつて本発明が不当に制限されるものでは
ない。 実施例 本例では安価な2相系鉄基合金としてFe−Mn
−Si3元系合金を使用した。 第1表に示す化学組成の溶湯を20〜2000rpmで
回転する直径300mmの超硬合金製双ロール、また
は400mmのCu製単ロール表面上に0.5×15mm口径の
ノズルより噴射し、50〜300μm厚、幅15mmの急
冷薄帯を作製した。鋳造まま、もしくはそれらの
いくつかについては熱間圧延と冷間圧延を組み合
せた処理をした後、直径15mmの端面をエメリー紙
で#600仕上げとした種々の接合素材で上記薄帯
をはさみN2ガス雰囲気中で局所的に高周波加熱、
所定の温度に昇温、所定の加圧力で所定の時間加
圧し放冷した。 これらより、平行部の直径10mm、長さ40mmの引
張試験片を切り出し、常温にて引張試験を行つ
た。それぞれの条件と試験結果を第2表に示す
が、本発明によつて容易に固相接合が行われるこ
とが分かる。
(Industrial Application Field) The present invention relates to a joining ribbon using an Fe-based alloy. (Conventional technology) Solid phase joining using superplastic materials is already well known [for example, ("Superplasticity and metal processing technology": edited by Superplasticity Research Group (1980), Nikkan Kogyo Shimbun, p. .151)]. However, in general, many superplastic materials are difficult to process in normal processing, and although there is an idea for solid-phase bonding in which a thin strip of superplastic material is sandwiched between a sandwich sandwich (Japanese Patent Application Laid-Open No. 52-45567), Practical implementation was difficult. In the case of solid phase bonding, the material must be formed into a thin strip with a thickness of several mm or less, and conventionally known superplastic materials could not be processed in this manner at industrial cost. (Problems to be Solved by the Invention) An object of the present invention is to provide an Fe-based alloy ribbon for solid phase bonding that exhibits superplasticity and eliminates the various drawbacks of the prior art as described above. (Means for Solving the Problems) Thus, the inventors of the present invention repeatedly studied various materials for solid phase bonding, and found that duplex stainless steels exhibiting superplasticity were particularly excellent. Further research will be carried out to specify the alloy composition, and if there is a problem with workability, it is preferable to form a thin strip by directly forming the molten metal, so that it can be formed at the same time as superplasticity. The present invention was completed based on the knowledge that Here, the gist of the present invention is to contain one or two of Si≧0.5% and Mn≧1.7% by weight, and Si eq=Si+2/3 (Cr+Mo) and Mn eq=
Si eq and specified by Mn+2Ni+60C+50N
Mn eq satisfies the following relationship, 5/6Si eq-15/2≦Mn eq≦11/5Si eq-77/5, and has an alloy composition in which the remainder substantially consists of Fe,
This is a Fe-based alloy ribbon for bonding. Furthermore, the present invention preferably produces a thin strip with excellent superplasticity directly from a molten metal by rapid solidification, and achieves an extremely short diffusion distance based on adhesion due to excellent flow utilizing the superplasticity. It is possible to realize the diffusion bonding method using the
The target material is not particularly limited, but iron alloys are more preferred. Also, according to the rapid solidification described above, the thickness is 2 mm.
The following ribbons can be easily manufactured without any problems with workability. (Function) Next, the reason why the alloy composition is limited as described above in the present invention will be described. First, the limited Si eq and
Mn eq defines the range in which the ratio of α/(α+γ) is 0.2 to 0.8 under hot working conditions of 700 to 1200°C, and as long as such conditions are satisfied, the specific composition of each individual Regardless of α/(α+γ)
=0.2 to 0.8 is satisfied, and superplasticity is achieved. Preferably, 1.1Si eq−10.8≦Mn eq≦1.7Si eq−
14, and Si eq = 10-20. The preferred range of Si eq and Mn eq is the range shown by diagonal lines in Figure 1, which will be described later. This is more preferable, and this is also preferable from the viewpoint of ensuring the properties of the product. FIG. 1 is a graph summarizing the above-mentioned relationship between Mn eq and Si eq. As is clear from what has already been said, Si eq and Mn eq were first defined as the Si equivalent of the ferrite-forming element, and
and to obtain the Mn equivalent of the austenite-forming elements. In the case of the present invention, in order to adjust the two-phase structure using Si and Mn, each is defined as described above. In addition, the reason why they are limited to the above range is that in this range, a two-phase structure of α phase and γ phase occurs, and the ratio of γ phase during hot working is 0.2 to 0.8, resulting in excellent superplasticity. This is because it will be done. Also, 0.5% or more Si or 1.7% or more Mn
The purpose of the present invention is to provide a superplastic Fe-based alloy that does not necessarily require corrosion resistance and is inexpensive.
This is because Si or Mn is actively used, and in the present invention, an amount greater than that conventionally used as a deoxidizing agent is added. In the present invention, the upper limits of Si and Mn are not particularly limited, but when considering Fe as the third element, in order to obtain the desired two-phase structure, Si<10
%, and Mn<15%, tissue adjustment becomes easier. Therefore, according to one preferred embodiment of the present invention, the alloy composition is Si: 0.5-10% by weight and/or Mn: 1.7-15%, balance Fe. In addition, from the purpose of obtaining the above-mentioned two-phase structure of the present invention, the amount of Ni, Cr, or Mo added is not limited, but for economic reasons, each
Ni: 0-5%, Cr: 0-20%, Mo: 0-2.5%
limited to. If you want to ensure corrosion resistance, you can increase the amount of Cr or Mo as necessary. Therefore, according to another aspect of the invention, the alloy composition is Si: 0.5-10% by weight, and/or Mn: 1.7-15% by weight, and Ni: 5% by weight.
Hereinafter, it is composed of at least one of Cr: 20% by weight or less and Mo: 2.5% by weight or less, the balance being Fe and unavoidable impurities. The two-phase alloy according to the present invention includes Fe, Si, Cr,
In addition to Mo, N and C, if necessary, Cu≦1.0
%, Ti≦0.5%, Zr≦0.5%, Nb≦0.5%, V≦0.5
%, W≦1.0%, as well as small amounts of Re, Ca, and Ce.
Also included in the present invention are those containing unavoidable impurities. However, since Ti, Zr, Nb, and V easily form nitrides and reduce the amount of solid solution N that is effective for superplasticity, it is better not to add them if possible. Since C may generate carbides and impair the properties of the product, a lower C content is preferable. N is a powerful γ-forming element, and it diffuses more easily than Mn and Ni. Therefore, it helps the structural changes caused by the thermal activation process, making it easier to develop superplastic deformation, and it is also the cheapest. It is advantageous to contain as much as possible, preferably about 0.01 to 0.25%. As described above, in the present invention, as long as the α+γ type two-phase structure is exhibited, the excellent superplasticity phenomenon can be utilized. It has been confirmed that as long as the conditions shown in FIG. 1 are satisfied, the α+γ two-phase structure is not substantially changed at all. The method of manufacturing the ribbon according to the present invention is not particularly limited, but considering that two-phase alloys are generally difficult-to-process materials, rapid solidification is preferable, and ordinary single roll, double roll, or other methods are preferable. Applicable. Although the cooling rate is not particularly limited, it is preferably 100° C./sec or more because the finer the structure, the better the subsequent superplastic deformability. More preferably it is 10 3 °C/sec or more. Further, the upper limit of the thickness of the ribbon is preferably 2 mm, since the thinner the thinner the thinner the cooling rate, the more efficient the bonding will be. Although there is no particular lower limit, it is set to 20 μm for reasons related to manufacturing the quenched ribbon. Although the thin strip obtained in this way can be used as is for solid-phase bonding, it is necessary to perform hot processing or cooling processing to improve the sheet surface properties and further refine the structure in the subsequent process. It's okay. These treatments significantly refine the structure through recrystallization during solid phase welding and improve superplasticity.
For this purpose, 50% and 20% or more are preferable, respectively. In order to achieve the above objective, the hot rolling temperature is preferably lower than 1200°C, more preferably 1000°C or lower.
It is best to do this at temperatures below ℃. When performing solid phase bonding using the ribbon for solid phase bonding obtained according to the present invention, the specific conditions are not particularly limited, but preferably, the bonding surface is first made a clean surface and then heated to 750 to 1200 ° C. Bonding may be performed while applying a pressure of 0.5 Kgf/mm 2 or more. The reason why the temperature is limited to 750 to 1200℃ is that it is easy to obtain the superplasticity of duplex stainless steel in this range, and the structure of the solid phase joining material will not become coarse and its original properties will not be impaired. It is. More preferably, the temperature is 900 to 1100°C. Heating may be performed by any method, but in order to prevent scaling, heating is preferably performed in an N 2 gas atmosphere containing a large amount of nitrogen, which is contained in a large amount in two-phase stainless steel. The compressive force for joining needs to be 0.5 Kgf/mm 2 or more, and if it is too large, buckling and deformation will increase, so it is desirable to keep it at 10 Kgf/mm 2 or less. Duplex stainless steel that has been joined by heating and pressure is cooled as it is, but if a sigma phase is formed during cooling, it will significantly impair toughness, so
Cool at a cooling rate of min or more, preferably 1000 ~
It is preferable to rapidly cool the material after heating it to around 1200.degree. C., since this is substantially the same as solution treatment. The material used for bonding is not particularly limited, but iron has good diffusion bonding properties and is unlikely to produce Kirkendall voids caused by significant differences in diffusion coefficients between different elements or intermediate phases consisting of intermetallic compounds that degrade mechanical properties. Base alloys are preferred, low alloy steels,
Austenitic and ferritic stainless steels can be used, and Ni-based alloys can also be used. Next, the present invention will be explained in more detail with reference to Examples, which are shown merely as examples of the present invention.
The present invention is not unduly limited thereby. Example In this example, Fe-Mn is used as an inexpensive two-phase iron-based alloy.
-Si ternary alloy was used. The molten metal having the chemical composition shown in Table 1 is sprayed onto the surface of a 300 mm diameter double roll made of cemented carbide or a 400 mm single Cu roll rotating at 20 to 2000 rpm from a nozzle with a diameter of 0.5 x 15 mm, and the thickness is 50 to 300 μm. A quenched ribbon with a width of 15 mm was prepared. Either as cast or after a combination of hot rolling and cold rolling for some of them, the above thin strips were sandwiched between various bonding materials with 15 mm diameter end faces finished with #600 emery paper and N2 Local high-frequency heating in a gas atmosphere,
The temperature was raised to a predetermined temperature, the pressure was applied at a predetermined pressure for a predetermined time, and the mixture was allowed to cool. From these, tensile test pieces with a parallel part diameter of 10 mm and a length of 40 mm were cut out and subjected to a tensile test at room temperature. The respective conditions and test results are shown in Table 2, and it can be seen that solid phase bonding is easily performed according to the present invention.

【表】【table】

【表】 3
*2:Mn eq=Mn+2Ni+60C+50N
*3:( )内NはTiNとして固定された残りの有効
(固溶)Nを示す。
[Table] 3
*2: Mn eq=Mn+2Ni+60C+50N
*3: N in parentheses is the remaining valid value fixed as TiN
(Solid solution) Indicates N.

【表】【table】

【表】 **:○:母材破断、△:接合部破断 強度は母
材並、×:接合部破断 強度母材破断
[Table] **: ○: Fracture of base metal, △: Fracture of joint, strength is same as base material, ×: Fracture of joint, strength of base material fracture

【図面の簡単な説明】[Brief explanation of the drawing]

添付図面は、本発明におけるMn eqとSi eqと
の関係を示すグラフである。
The accompanying drawing is a graph showing the relationship between Mn eq and Si eq in the present invention.

Claims (1)

【特許請求の範囲】 1 重量%で Si≧0.5%、およびMn≧1.7%の1種または2
種を含有し、かつ Si eq=Si+2/3(Cr+Mo)およびMn eq=
Mn+2Ni+60C+50Nで規定されるSi eqおよび
Mn eqが次式の関係を満足し、 5/6Si eq−15/2≦Mn eq≦11/5Si eq−77/5 残部実質的にFeからなる合金組成を有する、
固相接合用Fe基合金薄帯。 2 溶湯から直接に薄帯にまで成形された、特許
請求の範囲第1項記載の固相接合用Fe基合金薄
帯。 3 厚さが2mm以下である、特許請求の範囲第1
項または第2項記載の固相接合用Fe基合金薄帯。
[Claims] 1. One or two of Si≧0.5% and Mn≧1.7% in weight%
contains seeds and Si eq=Si+2/3(Cr+Mo) and Mn eq=
Si eq and specified by Mn + 2Ni + 60C + 50N
Mn eq satisfies the following relationship, 5/6Si eq-15/2≦Mn eq≦11/5Si eq-77/5, and has an alloy composition in which the remainder substantially consists of Fe,
Fe-based alloy ribbon for solid phase bonding. 2. The Fe-based alloy ribbon for solid phase bonding according to claim 1, which is formed directly from a molten metal into a ribbon. 3. The first claim in which the thickness is 2 mm or less
2. Fe-based alloy ribbon for solid phase bonding according to item 1 or 2.
JP7038286A 1986-03-28 1986-03-28 Thin fe alloy strip for solid phase joining Granted JPS62227598A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP7038286A JPS62227598A (en) 1986-03-28 1986-03-28 Thin fe alloy strip for solid phase joining

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7038286A JPS62227598A (en) 1986-03-28 1986-03-28 Thin fe alloy strip for solid phase joining

Publications (2)

Publication Number Publication Date
JPS62227598A JPS62227598A (en) 1987-10-06
JPH0524981B2 true JPH0524981B2 (en) 1993-04-09

Family

ID=13429836

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7038286A Granted JPS62227598A (en) 1986-03-28 1986-03-28 Thin fe alloy strip for solid phase joining

Country Status (1)

Country Link
JP (1) JPS62227598A (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2717344C (en) * 2008-03-19 2019-06-04 Hoeganaes Ab (Publ) Iron-chromium based brazing filler metal
JP6246478B2 (en) * 2013-03-28 2017-12-13 日新製鋼株式会社 Stainless steel heat exchanger component and method of manufacturing the same

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4444587A (en) * 1983-02-03 1984-04-24 Huntington Alloys, Inc. Brazing alloy

Also Published As

Publication number Publication date
JPS62227598A (en) 1987-10-06

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