JPS5940202B2 - Manufacturing method of ultra-low S1 free-cutting steel - Google Patents
Manufacturing method of ultra-low S1 free-cutting steelInfo
- Publication number
- JPS5940202B2 JPS5940202B2 JP54166410A JP16641079A JPS5940202B2 JP S5940202 B2 JPS5940202 B2 JP S5940202B2 JP 54166410 A JP54166410 A JP 54166410A JP 16641079 A JP16641079 A JP 16641079A JP S5940202 B2 JPS5940202 B2 JP S5940202B2
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- JP
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- Prior art keywords
- content
- refractory
- less
- free
- 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
Links
- 238000004519 manufacturing process Methods 0.000 title claims description 8
- 229910000915 Free machining steel Inorganic materials 0.000 title description 25
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 53
- 229910000831 Steel Inorganic materials 0.000 claims description 27
- 229910052681 coesite Inorganic materials 0.000 claims description 27
- 229910052906 cristobalite Inorganic materials 0.000 claims description 27
- 239000010959 steel Substances 0.000 claims description 27
- 229910052682 stishovite Inorganic materials 0.000 claims description 27
- 229910052905 tridymite Inorganic materials 0.000 claims description 27
- 239000000377 silicon dioxide Substances 0.000 claims description 26
- 235000012239 silicon dioxide Nutrition 0.000 claims description 25
- 239000011819 refractory material Substances 0.000 claims description 18
- 238000012545 processing Methods 0.000 claims description 7
- 229910020489 SiO3 Inorganic materials 0.000 claims description 2
- 238000003754 machining Methods 0.000 claims description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims 1
- 229910052802 copper Inorganic materials 0.000 claims 1
- 239000010949 copper Substances 0.000 claims 1
- 239000000203 mixture Substances 0.000 description 16
- 239000013078 crystal Substances 0.000 description 10
- 230000000694 effects Effects 0.000 description 10
- 229910052717 sulfur Inorganic materials 0.000 description 10
- 150000001875 compounds Chemical class 0.000 description 9
- 230000005496 eutectics Effects 0.000 description 9
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 8
- 239000011593 sulfur Substances 0.000 description 8
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 7
- 239000011449 brick Substances 0.000 description 7
- 238000012360 testing method Methods 0.000 description 6
- 239000000463 material Substances 0.000 description 5
- 238000009628 steelmaking Methods 0.000 description 5
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 4
- 238000005520 cutting process Methods 0.000 description 4
- 239000000395 magnesium oxide Substances 0.000 description 4
- 238000010587 phase diagram Methods 0.000 description 4
- 230000002378 acidificating effect Effects 0.000 description 3
- BYFGZMCJNACEKR-UHFFFAOYSA-N Al2O Inorganic materials [Al]O[Al] BYFGZMCJNACEKR-UHFFFAOYSA-N 0.000 description 2
- 229910001021 Ferroalloy Inorganic materials 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 229910000514 dolomite Inorganic materials 0.000 description 2
- 239000010459 dolomite Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229910000676 Si alloy Inorganic materials 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 239000011822 basic refractory Substances 0.000 description 1
- 229910002056 binary alloy Inorganic materials 0.000 description 1
- 238000010273 cold forging Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- KZHJGOXRZJKJNY-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Si]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O KZHJGOXRZJKJNY-UHFFFAOYSA-N 0.000 description 1
- -1 eMn Inorganic materials 0.000 description 1
- 230000005183 environmental health Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 230000012447 hatching Effects 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 229910052960 marcasite Inorganic materials 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052863 mullite Inorganic materials 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000011821 neutral refractory Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- NIFIFKQPDTWWGU-UHFFFAOYSA-N pyrite Chemical compound [Fe+2].[S-][S-] NIFIFKQPDTWWGU-UHFFFAOYSA-N 0.000 description 1
- 229910052683 pyrite Inorganic materials 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000010079 rubber tapping Methods 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
- 150000003463 sulfur Chemical class 0.000 description 1
- 230000003746 surface roughness Effects 0.000 description 1
- 230000001360 synchronised effect Effects 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Landscapes
- Compositions Of Oxide Ceramics (AREA)
- Treatment Of Steel In Its Molten State (AREA)
Description
【発明の詳細な説明】
本発明は低Si快削鋼、特に鋼中のSiが0、005以
下の被削性及び冷間加工性に優れた極低Si快削鋼の製
造方法に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing low-Si free-cutting steel, particularly ultra-low-Si free-cutting steel with Si content of 0.005 or less and excellent machinability and cold workability. be.
快削鋼の種類としては従来より硫黄或は鉛を添加した硫
黄快削鋼或は鉛削鋼が最も一般的に知られており、又C
a1Ti、Zr等の特殊元素を添加したCa快削鋼、T
i−Ca快削鋼、Zr快削鋼等も近年になって製造、使
用されるようになった。The most commonly known types of free-cutting steel are sulfur- or lead-added sulfur-free-cutting steel and lead-cutting steel.
a1 Ca free-cutting steel added with special elements such as Ti and Zr, T
i-Ca free-cutting steel, Zr free-cutting steel, etc. have also come to be manufactured and used in recent years.
ところで、加工面で汎用性の高い鉛快削鋼が数年前から
環境衛生上の問題からその使用に制約を受始め、これに
伴って硫黄快削鋼が改めて認識されるに至った。By the way, several years ago, the use of lead free-cutting steel, which is highly versatile in terms of machining, began to be restricted due to environmental health issues, and as a result, sulfur free-cutting steel has come to be recognized once again.
この硫黄快削鋼(P等の他元素を複合させたものを含む
月ま、適量のMnSを鋼中に介在させ、このMnSの内
部切欠効果によって被削性を高めるもので、その成分は
第1表のJIS規格に示す通りである。In this sulfur free-cutting steel (containing composites of other elements such as P), an appropriate amount of MnS is interposed in the steel, and the machinability is improved by the internal notch effect of this MnS. It is as shown in the JIS standard in Table 1.
以下、本発明を上記硫黄快削鋼を中心に詳述するが、本
発明はこれに限らず他の種類の快削鋼にも同様に適用で
きることはいうまでもない。Hereinafter, the present invention will be described in detail focusing on the above-mentioned sulfur free-cutting steel, but it goes without saying that the present invention is not limited to this and can be similarly applied to other types of free-cutting steel.
さて、快削鋼における被削性の評価は一般に工具寿命、
工具摩耗量、切削抵抗、切削処理性等によって行なわれ
るが、特に硫費央削鋼の場合、上記被剛性を向上させる
為には、鋼中のMnSの形状をより大きく、且つより丸
くすることが肝要となる。Now, the machinability of free-cutting steel is generally evaluated based on tool life,
This is done depending on the amount of tool wear, cutting resistance, cutting processability, etc., but especially in the case of sulfur-cutting steel, in order to improve the above-mentioned rigidity, it is necessary to make the shape of MnS in the steel larger and rounder. is essential.
そして、さらにこのMnSの形状を制御する手段として
は鋼中のSi含有量を可及的に低く抑制することが有効
であるとされている。Further, as a means of controlling the shape of this MnS, it is said that it is effective to suppress the Si content in the steel as low as possible.
一方、冷圧性(冷間圧造性)等の冷間加工性についても
鋼中のSiが低いほど良好となる。On the other hand, the lower the Si content in the steel, the better the cold workability such as cold pressability (cold forging property).
従って、快削鋼を製造するに当っては、被削性と冷間加
工性の両面から鋼中のSi含有量を低レベルに抑ff1
lJ、保持することが極めて重要な技術的課題として位
置付けられる。Therefore, when manufacturing free-cutting steel, it is necessary to keep the Si content in the steel to a low level from both machinability and cold workability.
lJ, and maintaining it is positioned as an extremely important technical issue.
硫黄快削鋼の製造は、一般に転炉等の製鋼炉で精錬、溶
製された溶鋼をシャモット、ロウ石等の酸性レンガで内
張すされた取鍋に装入(出鋼)し、F eMn −F
e S 2、FeP等の合金鉄を添加して脱酸、及び成
分調整を施した後、この溶鋼を鋳型に注入して鋼塊とな
し、これを圧延、二次加工するものであるが、従来鋼中
Siを低レベルに維持する為に上記製鋼並びに溶鋼処理
段階において、王として■低Si合金鉄の使用、■製鋼
炉での81の低減等の方案が採られている。Generally, sulfur free-cutting steel is produced by charging (tapping) molten steel that has been refined and melted in a steelmaking furnace such as a converter into a ladle lined with acidic bricks such as chamotte or waxite. eMn-F
After deoxidizing and adjusting the composition by adding ferroalloys such as eS2 and FeP, this molten steel is poured into a mold to form a steel ingot, which is then rolled and subjected to secondary processing. Conventionally, in order to maintain Si in steel at a low level, measures such as (1) use of low-Si alloy iron and (2) reduction of 81 in the steelmaking furnace have been adopted at the above-mentioned steelmaking and molten steel processing stages.
ところがこれらの対案によっても鋼中のSi(組下Si
値)を安定して(1010%以下にすることが困難であ
り、現実に0.006〜0.026%というバラツキを
見せており、ましてや0.005%以下の極低レベルを
達成、維持することは実操業では不可能であった。However, even with these countermeasures, Si in steel (Si under assembly)
It is difficult to stably reduce the value (value) to 1010% or less, and in reality there is a variation of 0.006 to 0.026%, much less to achieve and maintain an extremely low level of 0.005% or less. This was not possible in actual operation.
そこで本発明者等は上記■、■の方案の限界に鑑み、特
に溶鋼の処理環境に着目して、種々実験、研究を積み重
ねたところ、溶鋼処理(保持、運搬を含む少過程で耐火
容器として用いられる取鍋の内張耐火物からのSiの混
入が鍋中Siの低下を阻害している原因であることを究
明した。Therefore, in view of the limitations of the above-mentioned methods ① and ②, the inventors of the present invention have conducted various experiments and research, paying particular attention to the molten steel processing environment. It was determined that the contamination of Si from the refractory lining of the ladle used was the cause of inhibiting the reduction of Si in the ladle.
その結果、到達したのが本発明であり、その要旨は製鋼
炉で精錬、溶製された溶鋼を、内張り耐火壁の全部又は
一部が、A1203−8iO2系耐火物(SiO2含有
量30%以下)、CaO−Al2O:、−8i02系耐
火物(SiO2含有量30%以下)、MgO−Al2O
35i02系耐火物(SiO2含有量30%以下)、C
aO5102系耐火物(SiO2含有量50%以下)、
CaO−(VgOS i02系耐火物(SiO2含有量
50%以下)、MgO−8i02系耐火物(SiO2含
有量含有量6王
選択される1種以上の耐火物で構成された耐火容器に、
装入して処理を行なう硫黄快削鋼の製造方法に存する。As a result, we have arrived at the present invention, and its gist is that molten steel refined and melted in a steelmaking furnace is made of A1203-8iO2-based refractory (with a SiO2 content of 30% or less), in whole or in part, of the lining refractory wall. ), CaO-Al2O:, -8i02-based refractory (SiO2 content 30% or less), MgO-Al2O
35i02 series refractory (SiO2 content 30% or less), C
aO5102 refractory (SiO2 content 50% or less),
CaO-(VgOS) i02-based refractory (SiO2 content 50% or less), MgO-8i02-based refractory (SiO2 content 6K) In a refractory container composed of one or more selected refractories,
It consists in a method for manufacturing sulfur free-cutting steel, which involves charging and processing.
耐火物は一般に酸性、中性及び塩基性のいずれかに分類
されるが、酸性のものはシャモットやロウ石系に代表さ
れるようにSiO2の含有量が高いものが多く、又高ア
ルミナ系耐火物等の中性耐火物や、ドロマイト系耐火物
、マグネシア系耐火物等の塩基性耐火物にもSiO2が
配合されている。Refractories are generally classified as acidic, neutral, or basic, and acidic ones often have a high content of SiO2, such as chamotte and waxite-based refractories, and high-alumina refractories SiO2 is also blended in neutral refractories such as aluminum and basic refractories such as dolomite refractories and magnesia refractories.
そしてこれらの耐火物は、単一の酸化物のみから成るも
のではなく、通常2元系或は3元系の混合物として存在
している。These refractories do not consist of only a single oxide, but usually exist as a binary or ternary mixture.
これらの混合物における各酸化物の結晶構成等について
は、周知の如く2元系或は3元系状態図を用いて説明さ
れているが、多元系の下においては、それらの混合比率
に応じて各種の共晶化合物が存在している。As is well known, the crystal structure of each oxide in these mixtures is explained using a binary or ternary phase diagram, but in a multi-component system, it depends on their mixing ratio. Various eutectic compounds exist.
従ってこの様な耐火物は、例えばアルミナ−シリカ系の
場合、At203やSiO□等の単一酸化物(以下単味
結晶という)同志が適当な比率で混然一体化しているの
ではなく、単味結晶と共晶化合物の結晶(上記の例では
3At203・2Si02:ムライト)が混合された状
態として存在する。Therefore, in the case of alumina-silica-based refractories, for example, single oxides (hereinafter referred to as single crystals) such as At203 and SiO The taste crystals and the crystals of the eutectic compound (3At203.2Si02: mullite in the above example) exist in a mixed state.
即ちSiO2について考えると、混合系の下では、Si
O2の単味結晶として存在するだけでなく、3AL20
3・2SiO7や3CaO−8iO2等の共晶化合物と
して存在する。That is, considering SiO2, under a mixed system, Si
In addition to existing as a single crystal of O2, 3AL20
It exists as eutectic compounds such as 3.2SiO7 and 3CaO-8iO2.
しかるに従来、使用されているシャモット、ロウ行系耐
火物のようにSiO2含有量が75〜80%と高く、実
質的に単味結晶として存在する5i02は、極めて酸化
活性(本明細書では活量と称す)が高いので、特に硫黄
快削鋼の如きMnレベルが高い(0,70%少溶鋼に接
すると、自ら還元されてSiとなり易く、5102+2
Mn−+81+2Mn0
で示される反応を起こしてMnを酸化し、Siが鋼中に
放出され一結局MnSの生成を抑制してしまう。However, 5i02, which has a high SiO2 content of 75 to 80% and exists essentially as a single crystal, such as chamotte and waxy refractories that have been used in the past, has extremely oxidizing activity (in this specification, activity Since the Mn level is high, especially in sulfur free-cutting steel (when it comes into contact with 0.70% slightly molten steel, it is easily reduced to Si by itself, and 5102+2
A reaction shown by Mn-+81+2Mn0 occurs to oxidize Mn, and Si is released into the steel, eventually suppressing the production of MnS.
これに対して共晶化合物中におけるSiO2の活量は小
さく、遊離のSiとして溶鋼中に放出されることは極め
て少ない。On the other hand, the activity of SiO2 in the eutectic compound is small, and it is extremely rare for it to be released into molten steel as free Si.
結局耐火物中のSiO2活量を小さくすることが低Si
化達成の上で極めて重要であることが判り、耐火物中の
SiO2活量を低下させることに主眼を置いて本研究を
行なった。In the end, reducing the SiO2 activity in refractories is
This study was conducted with the main focus on reducing the SiO2 activity in refractories, as this was found to be extremely important in achieving this goal.
しかるに耐火物中にわずかでもSiO2単味結晶が存在
すると、その絶対量を溶鋼中のSi量と比較した場合、
化学平衡論的には耐火物側の方が多くなるのは必然的で
あり、結局溶鋼中のSi量を高める方向に作用する。However, if even a small amount of SiO2 single crystal exists in the refractory, when its absolute amount is compared with the amount of Si in molten steel,
In terms of chemical equilibrium, it is inevitable that the amount of Si increases on the refractory side, which ultimately acts to increase the amount of Si in the molten steel.
そこで本発明においては、SiO2単味結晶が実質上存
在しない領域における組成の耐火物を用いることにした
。Therefore, in the present invention, it was decided to use a refractory having a composition in a region where SiO2 single crystals are substantially absent.
又状態図自体から明白である様に、共晶化合物の融点は
一般に低く、溶鋼の取扱い(操業)温度において耐火物
が溶融する様な組成であってはならない。Also, as is clear from the phase diagram itself, the melting point of the eutectic compound is generally low, and the composition should not be such that the refractory will melt at the handling (operating) temperature of molten steel.
この様なところから本発明においては、処理温度域で実
質的に5i02の単味結晶が存在しない組成の耐火物と
して本発明に係る前記耐火物を特定し、これらからなる
群から選択される少なくとも1種の耐火物によって耐火
容器を形成することとした。For this reason, in the present invention, the refractory according to the present invention is specified as a refractory having a composition in which substantially no single crystal of 5i02 is present in the treatment temperature range, and at least one selected from the group consisting of these refractories is specified. We decided to form a fireproof container using one type of refractory material.
そしてこの処理温度域とは実際の操業を考慮すると具体
的には1460’C−1760℃の温度範囲を指すもの
である。In consideration of actual operation, this processing temperature range specifically refers to a temperature range of 1460'C to 1760C.
次に上記多元系耐火物について本発明の条件を満足する
範囲を説明する。Next, the range that satisfies the conditions of the present invention regarding the multi-component refractories will be explained.
第1〜3図は2元系、第4〜6図は3元系の各状態図を
示すが、図中の白丸は共晶化合物を意味し夫々その組成
を付記した。Figures 1 to 3 show phase diagrams for a binary system, and Figures 4 to 6 show phase diagrams for a ternary system. The white circles in the figures mean eutectic compounds, and their compositions are appended to each.
尚第4〜6図では煩雑を避ける為に等温線の記載を省略
した。Note that in FIGS. 4 to 6, isothermal lines are omitted to avoid complication.
まず第1図では3A403・2SiO2が形成される領
域のS i 02含有率は約30%であり、A403−
8i02系(即ちアルミナ系ルこおいては、30%を超
えてSiO□を含有する組成にすると5t02の単味結
晶が存在L SiO2活量が大きくなり本発明にとって
は不都合であることが判る。First, in FIG. 1, the Si02 content in the region where 3A403.2SiO2 is formed is about 30%, and A403-
It can be seen that in the case of 8i02 type (that is, alumina type), if the composition contains more than 30% of SiO□, 5t02 single crystals will be present and the LSiO2 activity will increase, which is disadvantageous for the present invention.
従って本系統においてはSiO2含有率を30%以下に
する必要がある。Therefore, in this system, the SiO2 content must be 30% or less.
同様の趣旨において、第2図のCaO−8i02系では
SiO2含有率を50%以下とする必要があり、更に第
3図のMgO−8i02糸(マグネシア系)ではSiO
2含有率を60%以下としなければならない。To the same effect, in the CaO-8i02 series shown in Fig. 2, the SiO2 content must be 50% or less, and furthermore, in the MgO-8i02 thread (magnesia series) shown in Fig. 3, the SiO2 content must be 50% or less.
2 content must be 60% or less.
第4図のCaO−A4035in2系では各共晶化合物
Ca(l S 102−CaOA403 ・28102
−3A/!、203・2S102を結ぶラインより下側
の領域における組成を満足するものでなければならず、
SiO3の限界含有率はCaOやAt203の含有比率
によっても変化するが、少なくとも50%以下とすべき
であり、特に確実には30%以下とすることが望ましい
。In the CaO-A4035in2 system shown in Fig. 4, each eutectic compound Ca(l S 102-CaOA403 ・28102
-3A/! , it must satisfy the composition in the area below the line connecting 203 and 2S102,
Although the limit content of SiO3 varies depending on the content ratio of CaO and At203, it should be at least 50% or less, and particularly preferably 30% or less.
第5図のCaO−MgO5in2系(ドロマイト系)で
は、各共晶化合物CaO−8iO2−Ca0・2SiO
2Mg()SiO2を結ぶラインより下側の領域におけ
る組成を満足するものでなければならず、5i02の限
界含有率はCaOやMgOの含有比率によっても変化す
るが、少なくとも50%以下とすべきである。In the CaO-MgO5in2 system (dolomite system) shown in Figure 5, each eutectic compound CaO-8iO2-Ca0.2SiO
It must satisfy the composition in the region below the line connecting 2Mg()SiO2, and the limiting content of 5i02 varies depending on the content ratio of CaO and MgO, but it should be at least 50% or less. be.
第6図のMgOA4035i02系ではほぼ各共晶化合
物MgOMgO−8iO2−2・2A403・5 S
i 02−3A403・2SiO3を結ぶラインより下
側の領域における組成を満足するものでなければならず
、SiO2の含有率はMgOやAt203によっても変
化するが、少なくとも60%以下とする必要があり、特
に確実には30%以下とすることが望ましい。In the MgOA4035i02 system shown in Figure 6, almost each eutectic compound MgOMgO-8iO2-2.2A403.5S
It must satisfy the composition in the region below the line connecting i 02-3A403/2SiO3, and the content of SiO2 changes depending on MgO and At203, but it must be at least 60% or less. In particular, it is desirable to set it to 30% or less to be sure.
上記の様な組成条件を満足する耐火物を用いる耐火容器
の種類については、特段の制限を受けないが、現状の製
鋼処理システムを考慮すると、取鍋やタンデイツンユ類
に適用した場合、特に顕著な効果を発揮する。There are no particular restrictions on the type of fireproof container that uses a refractory that satisfies the above compositional conditions, but considering the current steelmaking processing system, there are particularly noticeable be effective.
しかし例えば取鍋への適用を考慮するに当って、取鍋内
耐火壁の全面に上記組成の耐火物を張設することは、経
踪的な高負担を招く。However, when considering application to a ladle, for example, installing a refractory having the above composition on the entire surface of the refractory wall inside the ladle would result in an unnecessarily high burden.
そこで実用上満足できる様な耐火物張設構造を見究める
べく、SiO2活量の高いロウ石レンガ(SiO2ニア
8%、A403:20%)とSiO2活量り低いアルミ
ナレンガ(Si02:16’AA4,03:82%少と
を適当な比率で組合わせて6種類の取鍋耐火壁を構成し
、転炉で吹錬、溶製した溶鋼をこれらの取鍋に装入しF
eMn、、FeS2及びFeP等の合金鉄で脱酸、成分
調整を施し実際に硫黄快削鋼の製造試験を行なった。Therefore, in order to investigate a refractory-lined structure that would be practically satisfactory, we used waxite bricks with high SiO2 activity (SiO2 Ni 8%, A403: 20%) and alumina bricks with low SiO2 activity (Si02:16'AA4, 03:6 types of ladle refractory walls are constructed by combining 82% and 82% less in appropriate ratios, and molten steel blown and melted in a converter is charged into these ladles.
Deoxidation and component adjustment were performed using ferroalloys such as eMn, FeS2, and FeP, and actual tests were conducted to produce sulfur free-cutting steel.
第2表はこうして得られた快削鋼の化学成分(組下成分
)の分析値を示すものである。Table 2 shows the analytical values of the chemical composition (assembled composition) of the free-cutting steel thus obtained.
(但し、Sj基以外平均値(X))
第7図は、この製造試験に用いられた取鍋耐火壁の具体
的な構造(第2表1〜■に相”U)を示ム図中のハツチ
ング入りレンガは、本発明の耐火物組成を満足するアル
ミナレンガを用いた部分、点点入りレンガは本発明の組
成を満足しないロウ石レンガを用いた部分を示す。(However, the average value (X) other than the Sj group) Figure 7 shows the specific structure of the ladle fireproof wall used in this manufacturing test (phase "U" in Table 2 1 to ■). Bricks with hatchings in the figure indicate parts using alumina bricks that satisfy the refractory composition of the present invention, and bricks with dots indicate parts using waxite bricks that do not satisfy the compositions of the present invention.
第2表の結果から明らかなように、本発明の条件を満足
する耐火物を少なくとも65%(具体的には取鍋側底部
少以上の面積に適用した場合(■〜■)鋼中のSi含有
量は平均値で0.006%以下、最大値でも0.009
%以下、最少値では0.003%以下となり、従来のも
の(I)と比較して極めて低いレベルが維持され、且つ
バラツキも非常に小さくなっており、さらにこれを80
%以上とすれば0.005%以下の極低Siレベルの快
削鋼が安定して得られることが判明する。As is clear from the results in Table 2, when the refractory that satisfies the conditions of the present invention is applied to at least 65% (specifically, a small area or more of the bottom area of the ladle side (■ to ■)), Si in the steel The average content is 0.006% or less, and the maximum content is 0.009%.
% or less, and the minimum value is 0.003% or less, which maintains an extremely low level compared to the conventional type (I), and the variation is also very small.
% or more, it turns out that free-cutting steel with an extremely low Si level of 0.005% or less can be stably obtained.
なお、鋼中のSiレベルの観点からすれば本発明の条件
を満たす耐火物を100%としたもの(■υ が良いが
、使用後に取鍋底部に付層、固化したスラグやメタルの
剥離作業更には耐火物のコスト等を考慮すると、特に取
鍋底部に上記耐火物を適用しそれ以外は従来の耐火物で
構成したもの(V)がむしろ好ましいと言える。In addition, from the viewpoint of the Si level in the steel, 100% refractory material that satisfies the conditions of the present invention (■υ is better, but after use, it is necessary to remove the slag and metal that have formed and solidified at the bottom of the ladle. Furthermore, considering the cost of the refractory, it is more preferable to use the refractory (V) in which the above refractory is applied to the bottom of the ladle, and the rest is made of conventional refractories.
さて、かかる製造試験によって得られた硫黄快削鋼をサ
ンプルとし、本発明によるもの(成分は、C: 0.0
8%、Mn : 1.15%、P : 0.072%、
S:0.308%、S言0−003%、取鍋構造;第2
表M)と従来法によるもの(成分は、C: 0.09%
、Mn:1.13%、P : 0.075%、S:0.
310%、Si:0.008%、取鍋構造;第2表I)
につき、被削性及び冷圧性の比較試験を行なった結果を
第8図及び第9図に示す。Now, the sulfur free-cutting steel obtained through the manufacturing test was taken as a sample, and the steel according to the present invention (component: C: 0.0
8%, Mn: 1.15%, P: 0.072%,
S: 0.308%, S word 0-003%, ladle structure; 2nd
Table M) and conventional method (component: C: 0.09%
, Mn: 1.13%, P: 0.075%, S: 0.
310%, Si: 0.008%, ladle structure; Table 2 I)
The results of a comparative test of machinability and cold pressability are shown in FIGS. 8 and 9.
第8図より工具摩耗量、仕上面荒さ共に切削個数が10
00個以上となると従来材は次第に増加していくが本発
明材はほとんど変りがなく、本発明材の被削性が優れて
いることを物語っている。From Figure 8, the number of pieces cut is 10 for both tool wear amount and finished surface roughness.
00 or more, the conventional material gradually increases, but the inventive material shows almost no change, which proves that the inventive material has excellent machinability.
又第9図から、無抱束、抱束を問わず本発明材が従来材
と比較し高圧縮率でも割れ発生が少なく、冷圧性が高い
ことが知れる。Furthermore, from FIG. 9, it can be seen that the material of the present invention, regardless of whether it is unbound or bundled, has less cracking even at a high compression rate and has high cold compressibility compared to the conventional material.
以上、説明した通り、本発明によれば鋼中のSi含有量
が0.01%以下、特に0.005%以下の極低Si快
削鋼を比較的容易な手段によって安定して製造すること
ができ、従って被削性並びに冷間加工性に優れた快削鋼
が得られるという顕著な効果が提供される。As explained above, according to the present invention, it is possible to stably produce ultra-low Si free-cutting steel with a Si content of 0.01% or less, particularly 0.005% or less, by relatively easy means. This provides the remarkable effect that a free-cutting steel with excellent machinability and cold workability can be obtained.
【図面の簡単な説明】
第1〜6図は状態図、第7図は取鍋における耐火壁の構
造例を示す模式図、第8図は快削鋼の被削性試験結果を
示すグラフ、第9図は同調の冷圧性試験結果を示すグラ
フである。[Brief explanation of the drawings] Figures 1 to 6 are state diagrams, Figure 7 is a schematic diagram showing a structural example of a fireproof wall in a ladle, Figure 8 is a graph showing machinability test results of free-cutting steel, FIG. 9 is a graph showing the results of a synchronous cold pressure test.
Claims (1)
iO2の系耐火物(S t 02含有量30%以下)、
CaOAl 203 S t 02系耐火物(S t
02含有量30易以下)、Mg0−A i203−
S i 02系耐火物(SiO2含有量含有量3王 人物(SiO3含有量50%以下つ、C a 0−Mg
O−8 i 02系耐火物(SiO2含有量含有量5
丁からなる群から選択される1棟以上の耐火物で構成さ
れた耐火容器に、製銅炉でm溶製された溶鋼を装入して
処理を行なうことを特徴とする極低Si快削鋼の製造方
法。[Claims] 1. All or part of the force of the lining refractory ζ A1203-8
iO2-based refractory (S t 02 content 30% or less),
CaOAl 203 S t 02 series refractory (S t
02 content 30% or less), Mg0-A i203-
S i 02 series refractories (SiO2 content content 3 king figures (SiO3 content 50% or less), Ca 0-Mg
O-8 i 02 series refractory (SiO2 content content 5
Ultra-low Si free machining characterized by processing by charging molten steel melted in a copper furnace into a refractory container made of one or more refractories selected from the group consisting of Method of manufacturing steel.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP54166410A JPS5940202B2 (en) | 1979-12-20 | 1979-12-20 | Manufacturing method of ultra-low S1 free-cutting steel |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP54166410A JPS5940202B2 (en) | 1979-12-20 | 1979-12-20 | Manufacturing method of ultra-low S1 free-cutting steel |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5687650A JPS5687650A (en) | 1981-07-16 |
| JPS5940202B2 true JPS5940202B2 (en) | 1984-09-28 |
Family
ID=15830896
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP54166410A Expired JPS5940202B2 (en) | 1979-12-20 | 1979-12-20 | Manufacturing method of ultra-low S1 free-cutting steel |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5940202B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0648502A (en) * | 1992-07-24 | 1994-02-22 | Nippon Heater Kiki Kk | Automatic classification and storage machine for empty can |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2542761B1 (en) * | 1983-03-15 | 1987-10-16 | Vallourec | PROCESS FOR MANUFACTURING HIGH-MACHINABILITY STEELS |
-
1979
- 1979-12-20 JP JP54166410A patent/JPS5940202B2/en not_active Expired
Non-Patent Citations (1)
| Title |
|---|
| JOURNAL OF METALS-29,30=1967 * |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0648502A (en) * | 1992-07-24 | 1994-02-22 | Nippon Heater Kiki Kk | Automatic classification and storage machine for empty can |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5687650A (en) | 1981-07-16 |
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