JPS5918461B2 - Red-bellied goldenrod - Google Patents
Red-bellied goldenrodInfo
- Publication number
- JPS5918461B2 JPS5918461B2 JP50156902A JP15690275A JPS5918461B2 JP S5918461 B2 JPS5918461 B2 JP S5918461B2 JP 50156902 A JP50156902 A JP 50156902A JP 15690275 A JP15690275 A JP 15690275A JP S5918461 B2 JPS5918461 B2 JP S5918461B2
- Authority
- JP
- Japan
- Prior art keywords
- nitrogen
- alloy
- raw material
- goldenrod
- bellied
- 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
Landscapes
- Continuous Casting (AREA)
- Treatment Of Steel In Its Molten State (AREA)
Description
【発明の詳細な説明】
本発明は例えば非晶質合金等の急冷凝固金属材料の耐食
性、180°密着曲げ等の材料特注を改善することを目
的とした製造方法に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a manufacturing method aimed at improving the corrosion resistance of rapidly solidified metal materials such as amorphous alloys and customizing materials such as 180° close bending.
例えばFe−P−C−Cr等を主成分とする急冷凝固合
金(以下単に非晶質合金という。For example, a rapidly solidified alloy (hereinafter simply referred to as an amorphous alloy) whose main component is Fe-P-C-Cr.
)は、強度、耐食性とともに180°密着曲げ註にすぐ
れている。) has excellent strength, corrosion resistance, and 180° close bending notes.
ことが必要である。It is necessary.
特に窒素は耐食性を向上させるために効果がある。Nitrogen is particularly effective in improving corrosion resistance.
なお、急冷凝固金属材料の180°密着曲げ注は、種々
の因子によって低下するが、特に合金の結晶化が進行す
ると著しく低下する。Note that the 180° close bending of the rapidly solidified metal material decreases depending on various factors, but particularly as the crystallization of the alloy progresses, it decreases significantly.
ところで非晶質合金を製造するには、所望成分範囲に調
整した溶融金属を例えば106°C/秒の速度で急冷凝
固させるのであるが、窒素を添加する場合窒素合金の形
で、添加するのが普通である。By the way, in order to produce an amorphous alloy, molten metal adjusted to a desired composition range is rapidly solidified at a rate of, for example, 106°C/sec. When nitrogen is added, it is added in the form of a nitrogen alloy. is normal.
非晶質合金への窒素添加量はステンレス鋼における窒素
の添加量からの類推から0.3 % (重量)程度が必
要と考えられている。The amount of nitrogen added to the amorphous alloy is considered to be approximately 0.3% (by weight) by analogy with the amount of nitrogen added to stainless steel.
しかし本発明者等は種々研究の結果、非晶質合金中に必
要とされる窒素量はたかだか0.03%(重量)程度で
よいことを確認した。However, as a result of various studies, the present inventors have confirmed that the amount of nitrogen required in the amorphous alloy is at most about 0.03% (by weight).
すなわち、従来実施されている窒素合金の添加方法では
合金中に窒素以外の元素が含まれていることを確認した
。That is, it was confirmed that the conventional method of adding nitrogen alloys contains elements other than nitrogen in the alloy.
また、非晶質合金における重要な特性である180°密
着曲げ姓や延性が劣ること。In addition, it is inferior in 180° close bending and ductility, which are important properties in amorphous alloys.
また合金コストが高くなる等の商題点があることも確認
した。It was also confirmed that there were commercial problems such as high alloy costs.
本発明は、このような知見に基すいてなされたものであ
って、非晶質合金原料に窒素合金を使用せず該原料を窒
素雰囲気中で溶融して加窒し、該溶融金属を所望の形状
に急冷凝固させることを特徴とするものである。The present invention was made based on such knowledge, and instead of using a nitrogen alloy as an amorphous alloy raw material, the raw material is melted and nitrided in a nitrogen atmosphere, and the molten metal is converted into a desired material. It is characterized by being rapidly solidified into the shape of
本発明の合金の窒素含有量は、雰囲気制御の可能な溶解
炉を使用して、雰囲気中の窒素ガス圧力または窒素と不
活性ガスとを混合させて窒素分圧を変化させた状態で合
金を溶製することによって制御できる。The nitrogen content of the alloy of the present invention is determined by melting the alloy using a melting furnace that can control the atmosphere and changing the nitrogen gas pressure in the atmosphere or the nitrogen partial pressure by mixing nitrogen and an inert gas. It can be controlled by melting.
また前述のような方法で溶製した含窒素合金は、冷却後
も成分が変化することはほとんどないことから、そのま
ま再溶解して原料とすることも可能である。Further, since the nitrogen-containing alloy melted by the method described above hardly changes in composition even after cooling, it is possible to remelt it as it is and use it as a raw material.
実施例
500g溶解炉を用いて、第1表に示す成分の合金を溶
製した。EXAMPLE An alloy having the components shown in Table 1 was melted using a 500g melting furnace.
その際A1〜3はアルゴンガス雰囲気中で窒化クロムを
使用し、A4,5は窒素ガス雰囲気下で、A6は窒素と
アルゴンガスとの混合した雰囲気中で原料を溶解して、
遠心急冷法によりリボン状非晶質合金を製造した。At that time, for A1 to 3, chromium nitride was used in an argon gas atmosphere, for A4 and 5, the raw material was dissolved in a nitrogen gas atmosphere, and for A6, the raw material was dissolved in a mixed atmosphere of nitrogen and argon gas.
Ribbon-shaped amorphous alloys were manufactured by centrifugal quenching.
得られたリボン状非晶質合金は、厚さ20〜50μ、巾
約1 mm、長さ約300mmであった。The obtained ribbon-shaped amorphous alloy had a thickness of 20 to 50 μm, a width of about 1 mm, and a length of about 300 mm.
このようにして窒素合金を使用しないで製造した本発明
方法による製品と、窒素合金を用いて合金中に窒素を添
加した場合の製品の特性を第1表に対比して示す。Table 1 compares the characteristics of the product manufactured by the method of the present invention without using a nitrogen alloy and the product manufactured using a nitrogen alloy with nitrogen added to the alloy.
耐食性は、各方法によって製造した非晶質合金から50
龍長の試料を採取し、100℃の5係硫□酸液中に6時
間浸漬後の重量変化を測定した。The corrosion resistance was 50% from the amorphous alloy produced by each method.
A sample of the dragon length was taken and the weight change was measured after immersing it in a 100° C. pentahydric sulfuric acid solution for 6 hours.
表中の耐食性100は重量変化が全くなかったことを示
す。Corrosion resistance of 100 in the table indicates that there was no weight change at all.
また、得られた非晶質合金の薄片を180°に密着曲げ
を行なって折損の状騒を調査した。Further, the obtained amorphous alloy thin piece was closely bent at 180° and the state of breakage was investigated.
180゜密着曲げX印は折損を、○印は折損せず良好な
曲げ性を示すことを表わしている。180° close contact bending X marks indicate breakage, and O marks indicate good bendability without breakage.
* ;5%H2SO4,100℃X6hr浸漬試験で
の重量減量率この表から明らかなように窒素合金を使用
し、窒素を添加した非晶質合金成分は本発明方法により
作成したものに比べSiが多い。* ; Weight loss rate in 5% H2SO4, 100°C x 6hr immersion test As is clear from this table, the amorphous alloy component using nitrogen alloy and adding nitrogen has less Si compared to the one made by the method of the present invention. many.
また窒素合金を使用した場合の180°密着曲げは、窒
素が0.013係(重量)程度であっても不良であるが
、本発明により製造した非晶質合金は0.03%(重量
)の窒素を含んでいても180°曲げは良好であった。In addition, when using a nitrogen alloy, 180° close bending is poor even if the nitrogen content is about 0.013% (weight), but the amorphous alloy manufactured by the present invention has a nitrogen content of 0.03% (weight). Even though it contained nitrogen, 180° bending was good.
これらのことから窒素合金を使用すると、Siあるいは
窒素合金中の結晶性未溶解窒化物の存在が180°曲げ
を低下させたものと考えられる。From these facts, it is considered that when a nitrogen alloy is used, the presence of crystalline undissolved nitride in Si or the nitrogen alloy reduces 180° bending.
以上説明したように本発明によれば、目的とする添加元
素以外の元素が混入することを防止することができ、従
って合金構成を正確に保証することができ、材質安定に
寄与することができる。As explained above, according to the present invention, it is possible to prevent elements other than the intended addition elements from being mixed in, and therefore the alloy composition can be accurately guaranteed, contributing to material stability. .
さらには窒素合金を使用しないことから秤量、投入等の
工程の省略をすることができ、従って製造コストの低減
をはかることができる等、その効果は大きい。Furthermore, since no nitrogen alloy is used, steps such as weighing and charging can be omitted, and therefore manufacturing costs can be reduced, which has great effects.
Claims (1)
−P−C−Cr系原料を窒素雰囲気中で溶融し、所望成
分範囲に調整した溶融金属を、所望の形状に急冷凝固さ
せることを特徴とする急冷凝固金属材料の製造方法。1 Fe without using nitrogen alloy as alloy raw material
- A method for producing a rapidly solidified metal material, which comprises melting a P-C-Cr-based raw material in a nitrogen atmosphere and rapidly solidifying the molten metal, which has been adjusted to a desired composition range, into a desired shape.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP50156902A JPS5918461B2 (en) | 1975-12-29 | 1975-12-29 | Red-bellied goldenrod |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP50156902A JPS5918461B2 (en) | 1975-12-29 | 1975-12-29 | Red-bellied goldenrod |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5281010A JPS5281010A (en) | 1977-07-07 |
| JPS5918461B2 true JPS5918461B2 (en) | 1984-04-27 |
Family
ID=15637886
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP50156902A Expired JPS5918461B2 (en) | 1975-12-29 | 1975-12-29 | Red-bellied goldenrod |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5918461B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0686646B2 (en) * | 1990-03-05 | 1994-11-02 | 新日本製鐵株式会社 | Soft magnetic alloy ribbon |
-
1975
- 1975-12-29 JP JP50156902A patent/JPS5918461B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5281010A (en) | 1977-07-07 |
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