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JPS5813620B2 - Stainless steel - Google Patents
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JPS5813620B2 - Stainless steel - Google Patents

Stainless steel

Info

Publication number
JPS5813620B2
JPS5813620B2 JP49091315A JP9131574A JPS5813620B2 JP S5813620 B2 JPS5813620 B2 JP S5813620B2 JP 49091315 A JP49091315 A JP 49091315A JP 9131574 A JP9131574 A JP 9131574A JP S5813620 B2 JPS5813620 B2 JP S5813620B2
Authority
JP
Japan
Prior art keywords
steel
inclusions
cutting
chromium
stainless steel
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
Application number
JP49091315A
Other languages
Japanese (ja)
Other versions
JPS5118914A (en
Inventor
阿部山尚三
伊藤哲朗
高橋徹夫
木村篤良
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.)
Daido Steel Co Ltd
Original Assignee
Daido Steel Co 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 Daido Steel Co Ltd filed Critical Daido Steel Co Ltd
Priority to JP49091315A priority Critical patent/JPS5813620B2/en
Publication of JPS5118914A publication Critical patent/JPS5118914A/en
Publication of JPS5813620B2 publication Critical patent/JPS5813620B2/en
Expired legal-status Critical Current

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Description

【発明の詳細な説明】 本発明は(1)クロム、クロムとニッケル、マンガンと
クロムとニッケルを主合金成分とするオーステナイト系
、フエライト系およびマルテンサイト系ステンレス鋼に
被削性改善合金成分としてカルシウム0.006〜0,
06%とさらにイオウ0,05〜0,35%、鉛0,0
3〜0,30%、セレン0,03〜0,25%、テルル
0,01〜0.20%、ビスマス0,03〜0,30%
のいずれか1種以上とを添加含有せしめ、残余が実質的
に鉄よりなるステンレス鋼において該鋼中にC系または
C+B系介在物とA2系介在物との複合介在物を均等に
分散させたことを特徴とする複合非金属介在物を含有す
る快削ステンレス鋼。
Detailed Description of the Invention The present invention provides (1) adding calcium as a machinability-improving alloying component to austenitic, ferritic, and martensitic stainless steels whose main alloy components are chromium, chromium and nickel, or manganese, chromium, and nickel; 0.006~0,
0.06% and further sulfur 0.05-0.35%, lead 0.0
3-0.30%, selenium 0.03-0.25%, tellurium 0.01-0.20%, bismuth 0.03-0.30%
In a stainless steel in which the remainder is substantially iron, composite inclusions of C-based or C+B-based inclusions and A2-based inclusions are uniformly dispersed in the steel. A free-cutting stainless steel containing composite nonmetallic inclusions.

および(2)クロム、クロムとニッケル、マンガンとク
ロムとニッケルを主合金成分とし、さらにモリブデン、
アルミニウム、鋼、チタン、ニオブ+タンタル、窒素の
1種以上を含有せしめたオーステナイト系、マルテンサ
イト系オーステナイト・フエライト系および析出硬化系
ステンレス鋼に被削性改善成分としてカルシウム0.0
06〜0,06%とさらにイオウ0,05〜0,35%
、鉛0,03〜0,30%、セレン0,03〜0,25
%、テルル0,01〜0,20%、ビスマス0,03〜
0,30%のいずれか1種以上とを添加含有せしめ残余
が実質的に鉄からなるステンレス鋼において、該鋼中に
C系またはC+B系介在物とA2系介在物との複合介在
物を均等に分散させたことを特徴とする複合介在物を含
有する快削ステンレス鋼に関するものである。
and (2) chromium, chromium and nickel, manganese, chromium and nickel as main alloy components, and molybdenum,
Calcium 0.0 is added to austenitic, martensitic, austenitic/ferritic, and precipitation hardening stainless steels containing one or more of aluminum, steel, titanium, niobium + tantalum, and nitrogen as a machinability-improving component.
0.06-0.06% and further sulfur 0.05-0.35%
, lead 0.03~0.30%, selenium 0.03~0.25
%, tellurium 0.01~0.20%, bismuth 0.03~
In stainless steel containing one or more of 0.0 and 30% and the remainder substantially consisting of iron, composite inclusions of C-based or C+B-based inclusions and A2-based inclusions are evenly distributed in the steel. The present invention relates to a free-cutting stainless steel containing composite inclusions, which are characterized by being dispersed in.

而して不発明鋼の製造法の一例においては対象とするス
テンレス鋼の鋳造過程において、あらかじめ該鋼溶湯中
の酸素量を調整したのち一部のカルシウム・シリサイド
を取鋼中に置注ぎし、残余のカルシウム・シリサイドを
鋳込溶湯中に添加し、さらに他の快削性成分の規定量を
含有せしめて得られたC系またはB+C系介在物とA2
系介在物を均等に分散させることにより得られる。
In one example of a method for manufacturing non-inventive steel, during the casting process of the target stainless steel, the amount of oxygen in the molten steel is adjusted in advance, and then some calcium silicide is poured into the steel. C-based or B+C-based inclusions obtained by adding the remaining calcium silicide to the casting molten metal and further containing specified amounts of other free-machining components and A2
It is obtained by uniformly dispersing system inclusions.

ステンレス鋼を切削加工する場合、鋼の延性が高く熱伝
導性が小さいため切削による発熱量が大で、しかも工具
と切くず間の摩擦熱が逃げ難いなどの理由でムシレ、カ
ジリ、焼付きなどが生じ易い。
When cutting stainless steel, the heat generated by cutting is large because the steel has high ductility and low thermal conductivity, and the frictional heat between the tool and the chip is difficult to escape, resulting in cracking, galling, seizure, etc. is likely to occur.

このため、イオウ、鉛、セレン、鋼などの被削性改善合
金元素を少量含有させた快削ステンレス鋼が普及してい
る。
For this reason, free-cutting stainless steel containing small amounts of machinability-improving alloying elements such as sulfur, lead, selenium, and steel has become popular.

しかるに、これらの被削性改善合金元素の含有により耐
食性および強度がかなり損なわれる。
However, the inclusion of these machinability-improving alloying elements considerably impairs corrosion resistance and strength.

このため、カルシウム含有快削ステンレス鋼が提案され
、上記の欠点がかなり解消するにいたった。
Therefore, calcium-containing free-cutting stainless steel was proposed, and the above-mentioned drawbacks were largely eliminated.

ところが、カルシウムをかなり多量に添加するため、添
加カルシウム合金の種類、添加量、溶解法によって、鋼
中の酸化物系介在物の形態は変化するがほとんどC系介
在物(JISGO555−1956、Ca−アルミネー
ト( AI 一Ca−0)が主体(一部硫化物を含むこ
とがある)の粒状酸化物が不規則に分散しているもの、
または前記B系介在物(アルミナを主体とする粒状酸化
物が不連続にならんでいるもの)が残留している。
However, since a fairly large amount of calcium is added, the form of the oxide inclusions in the steel changes depending on the type of calcium alloy added, the amount added, and the melting method, but most of the oxide inclusions are C-based inclusions (JISGO555-1956, Ca- Particulate oxides mainly composed of aluminate (AI-Ca-0) (may contain some sulfides) are irregularly dispersed;
Alternatively, the B-based inclusions (discontinuously arranged granular oxides mainly composed of alumina) remain.

これらの介在物は軟化溶融温度がA2系介在物(マンガ
ンーシリケートを主体とする延伸型介在物)にくらべて
高く、超硬合金工具切削のごとく、切削速度が大で切削
温度が高い場合工具摩耗の増大が抑制されるが、高速度
鋼工具切削のごとく、切削速度が低い場合、工具摩耗の
増大を抑制し難い。
These inclusions have a higher softening and melting temperature than A2-based inclusions (elongated inclusions mainly composed of manganese-silicate), and are difficult to use when cutting at high cutting speeds and high cutting temperatures, such as when cutting with cemented carbide tools. Although an increase in wear is suppressed, when the cutting speed is low, such as when cutting a high-speed steel tool, it is difficult to suppress an increase in tool wear.

またC系介在物は鋼を熱間加工するも塑性変形し難いた
め基地鉄とのなじみがよくなく、ミクロクラツク、キャ
ビテイが発生し易い。
In addition, C-based inclusions are difficult to plastically deform even when steel is hot-worked, so they do not blend well with the base iron, and microcracks and cavities are likely to occur.

そのようなキャビテイの存在によって強腐食性雰囲気に
おける耐食性が基本成分鋼のそれよりも劣る場合がある
Due to the presence of such cavities, the corrosion resistance in strongly corrosive atmospheres may be inferior to that of the basic component steel.

本発明はステンレス鋼中にC系またはC+Er系介在物
とA2系介在物とを複合共存させ、A2系介在物をもっ
てC系介在物存在による鋼の熱間加工時におけるミクロ
クラツクキャビテイの発生を完全に解消して耐食性劣化
を防止し、さらにA2系およびC系介在物により広範囲
の切削領域の被削性改善を目的として開発した快削ステ
ンレス鋼である。
The present invention allows C-type or C+Er-type inclusions and A2-type inclusions to coexist in a composite manner in stainless steel, and the A2-type inclusions prevent the occurrence of micro-crack cavities during hot working of steel due to the presence of C-type inclusions. This is a free-cutting stainless steel that was developed with the aim of completely eliminating corrosion resistance and preventing deterioration of corrosion resistance, and further improving machinability in a wide range of cutting areas with A2 and C inclusions.

このため基礎実験として第1表に示すようにSUS30
4系Caステンレス鋼において、従来鋼は炉中でアルミ
ニウム脱酸し溶鋼を取鍋に移注する間にCaSiを全量
添加して常法により凝固させていた。
For this reason, as a basic experiment, as shown in Table 1, SUS30
In conventional 4-series Ca stainless steel, aluminum was deoxidized in a furnace, and while the molten steel was being poured into a ladle, the entire amount of CaSi was added and solidified by a conventional method.

これに対し不発明鋼は、炉中でアルミニウムを添加せず
あらかじめ取鍋底に少量の低A I− C a S i
を2〜5Kg/t入れ置き後、溶鋼中の酸素量を100
〜600ppmに調整した溶鋼を該取鍋に移住して攪拌
混合(必要に応じ不活性ガス吹込みを行なう)させ、溶
鋼鎮静後鋳型鋳込み、溶鋼流に上記CaSiを5〜30
Kg/t添加し充分攪拌混合しつつ鋳型内で緩徐冷凝固
させた。
On the other hand, non-inventive steel does not add aluminum in the furnace and is made by adding a small amount of low AI-C a Si to the bottom of the ladle beforehand.
After placing 2 to 5 kg/t of molten steel, the amount of oxygen in the molten steel was reduced to 100 kg/t.
The molten steel adjusted to ~600 ppm is transferred to the ladle and stirred and mixed (inert gas is blown in if necessary). After the molten steel has calmed down, it is poured into a mold, and the above CaSi is added to the molten steel flow by 5 to 30 ppm.
Kg/t was added, and the mixture was slowly cooled and solidified in a mold while sufficiently stirring and mixing.

この結果、熱間製造した上記鋼材中、従来鋼の非金属介
在物(酸化物)はほとんどC系で占められているが、前
記の方法で製造した本発明鋼のそれは大部分複合したC
系の外周をA2系が包囲したC+A2系(第1図参照)
で占められている。
As a result, in the above-mentioned hot-produced steel materials, non-metallic inclusions (oxides) in the conventional steel are mostly composed of C-based compounds, whereas those in the steel of the present invention produced by the method described above are mostly composed of composite C.
C+A2 system where the outer periphery of the system is surrounded by A2 system (see Figure 1)
occupied by

この点について考察するに、 従来鋼では炉中添加によるアルミニウム脱酸によって、
溶鋼中の酸素はAI。
Considering this point, in conventional steel, by deoxidizing aluminum by adding it in the furnace,
Oxygen in molten steel is AI.

03として固定され、残余の酸素のほとんど全量が取鍋
添加したCadiによってCaO1S102と固定され
るため、Ca −アルミネートが生成して形状的にC系
介在物となるものと推定される。
It is estimated that almost all of the remaining oxygen is fixed as CaO1S102 by Cadi added in the ladle, so that Ca-aluminate is generated and becomes C-based inclusions in shape.

ところが、本発明鋼では炉中でアルミニウムを添加せず
最初少量のカルシウムシリサイドで取鍋脱酸するため、
この時点の少量のCaSiから介入するAlの全量は非
常に少量のため鋼中にCa−Mn−シリケートが生成し
てA2系介在物をつくる。
However, in the steel of the present invention, aluminum is not added in the furnace and the ladle is deoxidized first with a small amount of calcium silicide.
Since the total amount of Al intervening from the small amount of CaSi at this point is very small, Ca-Mn-silicate is generated in the steel to form A2-based inclusions.

しかし、もしこの場合少量のCaSiを添加せず全量の
CaSiを一度に添加するときはCaSiから介入する
Al全量はほぼ100%歩留りよく鋼中に添加される結
果となり、このためCa−Mnシリケートはほとんど生
成せず、主としてCa−アルミネートが大量に発生する
ことが従来からの実施試験で確認されている。
However, in this case, if the entire amount of CaSi is added at once without adding a small amount of CaSi, the entire amount of Al that intervenes from CaSi will be added to the steel with a nearly 100% yield, and therefore Ca-Mn silicate It has been confirmed in conventional tests that Ca-aluminate is hardly produced, and mainly Ca-aluminate is produced in large quantities.

つぎに、既に鋼中にCa−Mn−シリケートからなる介
在物が多量に生成しているため、鋳込溶鋼流に大部分の
カルシウムシリサイドとアルミニウムを加えるも、Ca
−アルミネートは大量に生成しない。
Next, since a large amount of inclusions made of Ca-Mn-silicate have already been formed in the steel, even if most of the calcium silicide and aluminum are added to the molten steel flow, Ca
- Aluminate is not produced in large quantities.

したがって本発明鋼にはC a −Mn −シリケート
とCa−アルミネートが混在することになり、これが鋳
型内で溶鋼が緩徐冷凝固するとき、高融点のCa−アル
ミネートがまず析出し、あとから多量に存在する低融点
のCa−Mn−シリケートが析出し、Caアルミネート
を核として吸着複合が促進され、C系介在物をA2系介
在物が被覆するものと推定する。
Therefore, in the steel of the present invention, Ca-Mn-silicate and Ca-aluminate coexist, and when the molten steel slowly cools and solidifies in the mold, Ca-aluminate with a high melting point precipitates first, and later. It is presumed that a large amount of low-melting-point Ca-Mn-silicate precipitates, promotes adsorption and compounding using Ca aluminate as a core, and covers C-based inclusions with A2-based inclusions.

なお、本発明鋼の合金組成は上記めとおり、被削性改善
元素としてカルシウムを0.006〜0,06%含有し
ているが、カルシウムが0.006%以下では超硬工具
寿命の延長効果が薄弱である。
As mentioned above, the alloy composition of the steel of the present invention contains 0.006 to 0.06% calcium as an element that improves machinability, but if calcium is 0.006% or less, it has no effect on extending the life of cemented carbide tools. is weak.

一方0,06%を超えるとかえって工具摩耗を促進する
ため好ましくない。
On the other hand, if it exceeds 0.06%, it is not preferable because it actually accelerates tool wear.

上記カルシウムと共存させる被削性改善成分としてイオ
ウ0,05〜0,35%、鉛0,03〜0,30%、セ
レン0,03〜0,25%、テルル0,01〜0,20
%、ビスマス0,03〜0,30%の1種または2種以
上を選択含有せしめるが、これらは従来より高速度鋼工
具の寿命延長に効果的な金属化合物または硫化物として
ステンレス鋼中に存在させるに好適である。
The machinability-improving components that coexist with the calcium are 0.05% to 0.35% sulfur, 0.03% to 0.30% lead, 0.03% to 0.25% selenium, and 0.01% to 0.20% tellurium.
%, bismuth from 0.03% to 0.30%, which exist in stainless steel as metal compounds or sulfides that are effective in extending the life of high-speed steel tools. It is suitable for

したがって、本発明鋼の合金組成のうち、被削性改善成
分としてカルシウムとイオウ、鉛、セレン、テルル、ビ
スマスとを複合含有せしめる。
Therefore, in the alloy composition of the steel of the present invention, a composite of calcium, sulfur, lead, selenium, tellurium, and bismuth is included as components for improving machinability.

本発明の基本的態様は、前記のとおり、クロム、クロム
とニッケル、クロムとニッケル、マンガンを主合金成分
とするオーステナイト系、フエライト系およびマルテン
サイト系のステンレス鋼を対象とする。
As mentioned above, the basic embodiment of the present invention is directed to austenitic, ferritic, and martensitic stainless steels whose main alloy components are chromium, chromium and nickel, chromium and nickel, and manganese.

J I Sに規格化された鋼種を挙げれば、オーステナ
イト系では、SUS201,202、301、302、
303、303Se1 304、304L1305、3
0 5Jl、308、3098,3108,316、
316L,316J1、316JIL,317、317
L,321、3 2 9J1、347、384、385
、XM7およびXM15J1であり、フエライト系では
、SUS405、429、430、430Fおよび43
4であり、マルテンサイト系では、SUS 40 3、
410、410S,410J1、416、420J1、
420J2、420F,431、440A1440B,
440Cおよび440Fである。
Examples of steel types standardized by JIS are SUS201, 202, 301, 302, and austenitic steels.
303, 303Se1 304, 304L1305, 3
0 5Jl, 308, 3098, 3108, 316,
316L, 316J1, 316JIL, 317, 317
L, 321, 3 2 9J1, 347, 384, 385
, XM7 and XM15J1, and ferrite type SUS405, 429, 430, 430F and 43
4, and martensitic type SUS 40 3,
410, 410S, 410J1, 416, 420J1,
420J2, 420F, 431, 440A1440B,
440C and 440F.

本発明の変更態様は、上記の、クロム、クロムとニッケ
ル、またはマンガンとクロムとニッケルを主合金成分と
し、さらにモリブデン4.0%以下、アルミニウム1.
5%以下、同5.0%以下、チタン1.2%以下、ニオ
ブ+タンタル1,2%以下および窒素0.25%以下の
いずれか1種または2種以上を含有させた、オーステナ
イト系、フエライト系、マルテンサイト系、オーステナ
イト・フエライト系または析出硬化系のステンレス鋼を
対象とする。
A modified embodiment of the present invention uses chromium, chromium and nickel, or manganese, chromium and nickel as main alloy components, and further includes molybdenum of 4.0% or less and aluminum 1.0%.
Austenitic, containing one or more of the following: 5% or less, 5.0% or less, titanium 1.2% or less, niobium + tantalum 1.2% or less, and nitrogen 0.25% or less; Targets ferritic, martensitic, austenitic/ferritic, or precipitation hardening stainless steels.

モリブデンは耐食性向上を目的として添加するものであ
り、アルミニウムは耐酸化性を意図して含有させるもの
であり、銅の存在は耐食性向上の効果を有し、チタンお
よびニオブ+タンタルは粒界腐食の改善を狙って加え、
また窒素は高温強度を高めるはたらきがある。
Molybdenum is added for the purpose of improving corrosion resistance, aluminum is added for oxidation resistance, copper has the effect of improving corrosion resistance, and titanium and niobium + tantalum prevent intergranular corrosion. Added with the aim of improving
Nitrogen also has the effect of increasing high-temperature strength.

これらの元素を添加するステンレス鋼にJIS規格鋼種
は、オーステナイト系、フエライト系およびマルテンサ
イト系はさきに挙げたとおりである。
The JIS standard steel types of stainless steel to which these elements are added are austenitic, ferrite, and martensitic, as mentioned above.

オーステナイト・フエライト系の鋼種としてはSUS3
29J1が代表的なものであり、析出硬化系のステンレ
ス鋼擾こは、SUS630、631および631Jなど
がある。
SUS3 is the type of austenitic/ferrite steel.
29J1 is a typical example, and precipitation hardened stainless steel paddles include SUS630, 631, and 631J.

上記の各種ステンレス鋼は、クロムを11〜28%、ニ
ッケルを30%以下、そしてマンガンを10%以下含有
する。
The various stainless steels mentioned above contain 11 to 28% chromium, 30% or less nickel, and 10% or less manganese.

以下、実施例をもって具体的に詳しく説明する。Hereinafter, the present invention will be specifically explained in detail using examples.

実施例 1 実験用溶解炉により第2表に示す化学成分の種種の系の
ステンレス鋼を製造し、ついで熱間鍛造により丸棒状(
直径60mm)試験片に成形し、さらに1100℃に加
熱保持する均質化焼鈍を施した。
Example 1 Stainless steels with the various chemical components shown in Table 2 were produced in an experimental melting furnace, and then hot forged into round bar shapes (
The specimen was formed into a test piece (diameter: 60 mm), and then subjected to homogenization annealing by heating and holding at 1100°C.

前記試験片から熱間ねじり試験片を採取し、通常の加熱
温度( 1000〜1200°C)およびひずみ速度(
1〜100SeC−1 )における熱間加工性を調査し
た結果、本発明鋼はいずれも比較鋼A2,A3とほぼ同
等であった。
A hot torsion test piece was taken from the test piece, and the normal heating temperature (1000-1200°C) and strain rate (
As a result of investigating the hot workability at temperatures of 1 to 100 SeC-1), all of the steels of the present invention were almost equivalent to comparative steels A2 and A3.

つぎに第2表に示す鋼材について、超硬合金工具および
高速度鋼工具による切削試験を行ない、各鋼材切削時の
所定の工具寿命に対応する切削速度をもって被削性の指
標とした。
Next, cutting tests were conducted using cemented carbide tools and high-speed steel tools for the steel materials shown in Table 2, and the cutting speed corresponding to a predetermined tool life when cutting each steel material was used as an index of machinability.

それを第3表に示す。It is shown in Table 3.

■)超硬合金工具による切削試験条件 工 具: P20 ( 0,7,7,7,1 0,0,
0.5R)送 り:0.18mm/rev. 切込み:0.6mm 切削油剤:なし(乾式切削) 切削速度:工具寿命が70分になるときの切削速度を特
性値とし、A1鋼のそ 孔を100としたときの比で示す。
■) Cutting test conditions using cemented carbide tools Tool: P20 (0,7,7,7,1 0,0,
0.5R) Feed: 0.18mm/rev. Depth of cut: 0.6 mm Cutting oil: None (dry cutting) Cutting speed: The cutting speed at which the tool life reaches 70 minutes is taken as a characteristic value, and is expressed as a ratio when the straight hole of A1 steel is set as 100.

■)高速度鋼工具による切削試験条件 工 具: SKH5 7 ( 0,1 5,7.7.
1 0,0,0.5 R)送 り: 0. 1 8m
m/ rev.切込み二0.6mm 切削油剤:なし(乾式切削) 切削速度:工具寿命が40分になるときの切削速度を特
性値とし、A1鋼のそ れを100としたときの比で示す。
■) Cutting test conditions using high-speed steel tools Tool: SKH5 7 (0, 1 5, 7.7.
1 0,0,0.5 R) Feed: 0. 18m
m/rev. Depth of cut 2: 0.6 mm Cutting oil: None (dry cutting) Cutting speed: The cutting speed at which the tool life reaches 40 minutes is taken as a characteristic value, and is expressed as a ratio when that of A1 steel is set as 100.

同表にみられるとおり、C系介在物にA2系介在物が付
着包被した複合介在物を均等に分散させた本発明鋼の被
削性は比較鋼A1,A2のそれに比べて約50〜110
%(超硬工具切削時)、約10〜30%(高速度鋼工具
切削時)の向上が得られた。
As shown in the same table, the machinability of the steel of the present invention, in which composite inclusions in which C-based inclusions are adhered and covered by A2-based inclusions, is evenly dispersed is approximately 50 to 50% higher than that of comparative steels A1 and A2. 110
% (when cutting carbide tools) and about 10 to 30% (when cutting high-speed steel tools).

超硬合金工具切削において被削材中の主としてカルシウ
ムよりなるC+A2系介在物が切削時に軟化あるいは溶
融してベラークとなり、これが工具の切刃面に付着して
工具摩耗を抑制するためと考えられる。
This is thought to be due to the fact that in cutting cemented carbide tools, C+A2-based inclusions mainly composed of calcium in the workpiece material soften or melt during cutting to form belag, which adheres to the cutting edge surface of the tool and suppresses tool wear.

またカルシウムとイオウ、セレン、テルル、鉛、ビスマ
スなどと共存させた被削材では工具一切くず接触域での
切欠き、潤滑作用でさらに被削性が助長されるためと考
えられる。
In addition, it is thought that in workpiece materials in which calcium and sulfur, selenium, tellurium, lead, bismuth, etc. coexist, machinability is further improved by notching and lubrication in the area where all tool chips come into contact.

つぎに、耐食性試験として、試験片を室温状態の1%硫
酸および1%塩酸に1時間浸漬したときの腐食減量(
g/m”/ h )を求め、A1鋼のそれを100とし
て比で第3表に併記した。
Next, as a corrosion resistance test, the corrosion loss (
g/m''/h) was determined and is also listed in Table 3 as a ratio, with that of A1 steel set as 100.

同表にみられるとおり、本発明鋼は比較鋼AOとほぼ同
等の耐食性を有することがわかつた。
As shown in the same table, it was found that the steel of the present invention had almost the same corrosion resistance as the comparative steel AO.

また本発明鋼中耐食性が劣るA11鋼でも、A1鋼に比
べて著しく優れている。
Furthermore, even A11 steel, which has poor corrosion resistance among the steels of the present invention, is significantly superior to A1 steel.

したがって本発明鋼が特定範囲内で上記被削性改善元素
を含有し、しかもC+A2系介在物が存在するも、耐食
性に悪影響を及ぼさないことが確認できた。
Therefore, it was confirmed that the steel of the present invention contains the above-mentioned machinability-improving elements within a specific range, and even in the presence of C+A2 inclusions, the corrosion resistance was not adversely affected.

実施例 2 実験用溶解炉により第4表に示す化学成分のフエライト
系ステンレス鋼を製造し、ついで熱間鍛造により丸棒状
(直径60mm)試験片に成形し、さらに820℃に加
熱保持する均質化焼鈍を施した。
Example 2 A ferritic stainless steel having the chemical composition shown in Table 4 was produced in an experimental melting furnace, then hot forged into a round bar-shaped test piece (diameter 60 mm), and homogenized by heating and holding at 820°C. Annealed.

前記試験片から熱間ねじり試験片を採取して実施例1と
同様に熱間加工性を調査した結果、本発明鋼はいづれも
比較鋼F1とほぼ同等であった。
Hot torsion test pieces were taken from the test pieces and hot workability was investigated in the same manner as in Example 1. As a result, all of the steels of the present invention were almost equivalent to comparative steel F1.

つぎに第4表に示す鋼材について、実施例1と同様な切
削試験を行ない、その被削性を第5表に示す。
Next, the steel materials shown in Table 4 were subjected to the same cutting test as in Example 1, and the machinability is shown in Table 5.

同表にみられるとおり、本発明鋼の被削性は比較鋼F1
のそれに比べて約50〜110%(超硬工具切削時)、
約20〜40%(高速度鋼工具切削時)の向上が得られ
た。
As seen in the same table, the machinability of the steel of the present invention is that of the comparative steel F1.
Approximately 50 to 110% compared to that of (when cutting carbide tools),
An improvement of about 20-40% (when cutting high-speed steel tools) was obtained.

このような作用効果が得られた理由は実施例1の場合と
同様であると考えられる。
The reason why such effects were obtained is considered to be the same as in Example 1.

つぎに耐食性についても実施例1の場合と同様に腐食減
量を求め、F1鋼のそれを100として比で第5表に併
記した。
Next, regarding the corrosion resistance, the corrosion weight loss was determined in the same manner as in Example 1, and is also listed in Table 5 as a ratio, setting that of F1 steel as 100.

同表にみられるとおり、本発明鋼は比較鋼FOとほぼ同
等の耐食性を有することがわかった。
As shown in the same table, it was found that the steel of the present invention had almost the same corrosion resistance as the comparative steel FO.

この点から、後述する範囲内でカルシウムとイオウ、鉛
、セレン、テルル、ビスマスのいづれか1種または2種
以上を複合含有し、しかもC+A2系介在物を分散させ
るも、基本成分鋼の耐食性を何等損なわないことがわか
った。
From this point of view, even if calcium and one or more of sulfur, lead, selenium, tellurium, and bismuth are contained in combination within the range described below, and C+A2 inclusions are dispersed, the corrosion resistance of the basic component steel will not be improved. It turned out that there was no damage.

実施例 3 実験用溶解炉により第6表に示す化学成分のマルテンサ
イト系ステンレス鋼を製造し、ついで熱間鍛造により丸
棒状(直径60mm)試験片に成形し、さらに850℃
に加熱保持する均質化焼鈍を施した。
Example 3 A martensitic stainless steel having the chemical composition shown in Table 6 was produced in an experimental melting furnace, then hot forged into a round bar (60 mm in diameter) test piece, and further heated at 850°C.
Homogenization annealing was performed by heating and holding.

前記試験片から熱間ねじり試験片を採取して実施例1と
同様に熱間加工性を調査した結果、本発明鋼は比較鋼M
l,M7とほぼ同等の熱間加工性を有することがわかつ
た。
A hot torsion test piece was taken from the test piece and the hot workability was investigated in the same manner as in Example 1. As a result, the present invention steel was compared to comparative steel M.
It was found that it had almost the same hot workability as M7.

つぎに第5表に示す鋼材について、実施例1と同様な切
削試験を行ない、その被削性を第7表に示す。
Next, the steel materials shown in Table 5 were subjected to the same cutting test as in Example 1, and the machinability is shown in Table 7.

同表にみられるとおり、416系本発明鋼M5の被削性
は比較鋼M1のそねこ比べて約30%(超硬工具切削時
)約20%(高速度鋼工具切削時)向上し、410系不
発明鋼M3,M4の被削性は比較鋼MOのそれに比べて
約80,100%(超硬工具切削時)、約120,1
50(高速度鋼工具切削時)向上していることがわかっ
た。
As shown in the same table, the machinability of the 416 series inventive steel M5 is improved by about 30% (when cutting carbide tools) and about 20% (when cutting high-speed steel tools) compared to the comparative steel M1. The machinability of the 410 series uninvented steels M3 and M4 is approximately 80,100% (when cutting carbide tools) and approximately 120,1% compared to that of the comparative steel MO.
50 (when cutting high-speed steel tools).

また440F系不発明鋼M12の被削性は比較鋼M7の
それに比べて約30%(超硬工具切削時)約15%(高
速度鋼工具切削時)向上し、440C系本発明鋼M9,
MIO,Mllの被削性は比較鋼M6のそれに比べて約
130%(超硬工具切削時)、約140〜165%(高
速度鋼工具切削時)向上していることがわかった。
In addition, the machinability of the 440F series inventive steel M12 is improved by about 30% (when cutting carbide tools) and about 15% (when cutting high speed steel tools) compared to that of the comparison steel M7, and the 440C series inventive steel M9,
It was found that the machinability of MIO and Mll was improved by about 130% (when cutting carbide tools) and about 140 to 165% (when cutting high-speed steel tools) compared to that of comparative steel M6.

つぎに耐食性についても実施例1の場合と同様に腐食減
量を求め、M1鋼およびMI鋼のそれを100として比
で第7表に併記した。
Next, regarding corrosion resistance, the corrosion weight loss was determined in the same manner as in Example 1, and the ratio is also shown in Table 7, with the values of M1 steel and MI steel set as 100.

同表にみられるとおり、416系本発明鋼M5の耐食性
は比較鋼M1のそれに比べてやや優れている。
As shown in the same table, the corrosion resistance of the 416 series inventive steel M5 is slightly superior to that of the comparative steel M1.

また410系本発明鋼M3,M4の耐食性は比較鋼MO
のそれと大差ないことがわかった。
In addition, the corrosion resistance of the 410 series inventive steel M3 and M4 is that of the comparative steel MO.
It turns out that there is not much difference from that of .

また440F,440C系本発明鋼および比較鋼につい
てもほぼ同様の傾向がみられた。
Moreover, almost the same tendency was observed for the 440F and 440C steels of the present invention and comparative steels.

以上のとおり、クロム、クロムとニッケル、マンガンと
クロムとニッケルを主合金成分とし、これに耐食性改善
合金成分を必要により適宜含有せしめた従来のフエライ
ト系、オーステナイト系、マルテンサイト系、オーステ
ナイト系および析出硬化系ステンレス鋼に、適量のカル
シウムと、更に適量のイオウ、鉛、セレン、テルル、ビ
スマスなどの被削性改善合金成分を複合添加し、鋼中に
C系またはC+B系介在物とA2系介在物との複合介在
物を均等に分散させた不発明鋼の被削性は従来のステン
レス鋼はもとより、C系介在物よりなるカルシウム含有
快削ステンレス鋼に比べて被削性が著しく向上し、熱間
加工性、耐食性はもちろん、材料強度も何ら遜色のない
ことを確認した。
As mentioned above, conventional ferrite, austenitic, martensitic, austenitic and Adding an appropriate amount of calcium to hardened stainless steel, as well as an appropriate amount of machinability-improving alloy components such as sulfur, lead, selenium, tellurium, and bismuth, creates C-based or C+B-based inclusions and A2-based inclusions in the steel. The machinability of non-inventive steel, which has composite inclusions evenly distributed with objects, is significantly improved compared to conventional stainless steel as well as calcium-containing free-cutting stainless steel made of C-based inclusions. It was confirmed that not only the hot workability and corrosion resistance but also the material strength were comparable.

【図面の簡単な説明】 第1図は本発明鋼A6中に存在するC+A2系介在物の
拡大写真(600倍)である。
BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 is an enlarged photograph (600 times) of C+A2 inclusions present in the steel A6 of the present invention.

Claims (1)

【特許請求の範囲】 1 クロム、クロムとニッケル、またはマンガンとクロ
ムとニッケルを主合金成分とするオーステナイト系、フ
エライト系、またはマルテンサイト系のステンレス鋼に
、被削性改善合金成分として、カルシウム0.006〜
0.06%と、イオウ0.05〜0.35%、鉛0.0
3〜0.30%、セレン0.03〜0.25%、テルル
0.01〜0.20%およびビスマス0.03〜0.3
0%のいずれか1種または2種以上とを添加し、残余が
実質的に鉄からなるステンレス鋼において、鋼中にC系
または(C+B)系の介在物と、A2系介在物との複合
介在物を均等に分散させたことを特徴とする複合非金属
介在物を含有する快削ステンレス鋼。 2 クロム、クロムとニッケル、またはマンガンとクロ
ムとニッケルを主合金成分とし、さらにモリブデン4.
0%以下、アルミニウム1.5%以下、銅5.0%以下
、チタン1.2%以下、ニオブ+タンタル1.2%以下
および窒素1.2%以下のいずれか1種または2種以上
を含有するオーステナイト系:フエライト系、マルテン
サイト系、オーステナイト・フエライト系または析出硬
化系のステンレス鋼に、被削性改善合金成分として、カ
ルシウム0.006〜0.06%と、イオウ0.05〜
0.35%、鉛0.03〜0.30%、セレン0.03
〜0.25%、テルル0.01〜0.20%およびビス
マス0.03〜0.30%のいずれか1種または2種以
上とを添加し、残余が実質的に鉄からなるステンレス鋼
において、鋼中にC系または(C十B)系の介在物とA
2系介在物との複合介在物を均等に分散させたことを特
徴とする複合非金属介在物を含有する快削ステンレス鋼
[Claims] 1. An austenitic, ferritic, or martensitic stainless steel whose main alloy components are chromium, chromium and nickel, or manganese, chromium, and nickel, with zero calcium added as a machinability-improving alloy component. .006~
0.06%, sulfur 0.05-0.35%, lead 0.0
3-0.30%, selenium 0.03-0.25%, tellurium 0.01-0.20% and bismuth 0.03-0.3
In stainless steel containing 0% of one or more of the above, the remainder being substantially iron, a composite of C-based or (C+B)-based inclusions and A2-based inclusions in the steel. A free-cutting stainless steel containing composite nonmetallic inclusions, characterized in that the inclusions are evenly distributed. 2. The main alloy components are chromium, chromium and nickel, or manganese, chromium and nickel, and molybdenum4.
0% or less, aluminum 1.5% or less, copper 5.0% or less, titanium 1.2% or less, niobium + tantalum 1.2% or less, and nitrogen 1.2% or less. Contains austenitic: ferrite, martensitic, austenite-ferrite, or precipitation hardening stainless steel, with 0.006 to 0.06% calcium and 0.05 to 0.05% sulfur as machinability-improving alloy components.
0.35%, lead 0.03-0.30%, selenium 0.03
-0.25%, tellurium 0.01-0.20% and bismuth 0.03-0.30%, and one or more of them are added, and the remainder is essentially iron. , C-based or (C+B)-based inclusions in steel and A
A free-cutting stainless steel containing composite nonmetallic inclusions, characterized in that composite inclusions with two-type inclusions are evenly dispersed.
JP49091315A 1974-08-09 1974-08-09 Stainless steel Expired JPS5813620B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP49091315A JPS5813620B2 (en) 1974-08-09 1974-08-09 Stainless steel

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP49091315A JPS5813620B2 (en) 1974-08-09 1974-08-09 Stainless steel

Publications (2)

Publication Number Publication Date
JPS5118914A JPS5118914A (en) 1976-02-14
JPS5813620B2 true JPS5813620B2 (en) 1983-03-15

Family

ID=14023021

Family Applications (1)

Application Number Title Priority Date Filing Date
JP49091315A Expired JPS5813620B2 (en) 1974-08-09 1974-08-09 Stainless steel

Country Status (1)

Country Link
JP (1) JPS5813620B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6119632A (en) * 1984-07-05 1986-01-28 Kyowa:Kk Elastic hydrophilic polymer and its production

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5333938B2 (en) * 1972-07-22 1978-09-18

Also Published As

Publication number Publication date
JPS5118914A (en) 1976-02-14

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