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JPS5833289B2 - Method for producing industrial pure iron using a bottom blowing converter - Google Patents
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JPS5833289B2 - Method for producing industrial pure iron using a bottom blowing converter - Google Patents

Method for producing industrial pure iron using a bottom blowing converter

Info

Publication number
JPS5833289B2
JPS5833289B2 JP53101866A JP10186678A JPS5833289B2 JP S5833289 B2 JPS5833289 B2 JP S5833289B2 JP 53101866 A JP53101866 A JP 53101866A JP 10186678 A JP10186678 A JP 10186678A JP S5833289 B2 JPS5833289 B2 JP S5833289B2
Authority
JP
Japan
Prior art keywords
blowing
gas
injected
converter
hot metal
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
JP53101866A
Other languages
Japanese (ja)
Other versions
JPS5528372A (en
Inventor
勇 五藤
恭二 中西
健一郎 鈴木
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.)
JFE Steel Corp
Original Assignee
Kawasaki Steel Corp
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 Kawasaki Steel Corp filed Critical Kawasaki Steel Corp
Priority to JP53101866A priority Critical patent/JPS5833289B2/en
Publication of JPS5528372A publication Critical patent/JPS5528372A/en
Publication of JPS5833289B2 publication Critical patent/JPS5833289B2/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21CPROCESSING OF PIG-IRON, e.g. REFINING, MANUFACTURE OF WROUGHT-IRON OR STEEL; TREATMENT IN MOLTEN STATE OF FERROUS ALLOYS
    • C21C5/00Manufacture of carbon-steel, e.g. plain mild steel, medium carbon steel or cast steel or stainless steel
    • C21C5/28Manufacture of steel in the converter
    • C21C5/30Regulating or controlling the blowing
    • C21C5/34Blowing through the bath

Landscapes

  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)

Description

【発明の詳細な説明】 この発明は、底吹き転炉による工業用純鉄の溶製方法に
関し、極低硫鋼の溶製に併せて他の不純物をも低下させ
ることにより、工業用純鉄を製造する方法である。
Detailed Description of the Invention The present invention relates to a method for producing industrial pure iron using a bottom blowing converter, and by reducing other impurities while producing ultra-low sulfur steel, it is possible to produce industrial pure iron. This is a method of manufacturing.

従来の酸素底吹き転炉は、炉底に酸素ガスなどの酸化性
ガスの流路と、羽目冷却用保護ガスの流路とからなる多
数の同心2重管羽口を具えている。
A conventional oxygen bottom-blown converter is equipped with a large number of concentric double-tube tuyeres at the bottom of the furnace, each consisting of a flow path for an oxidizing gas such as oxygen gas and a flow path for a protective gas for cooling the blades.

そして、それらの羽口のうちの精錬ガスの流路(内管)
から、酸化性ガスとともに燐や硫黄などの不純物除去の
ために、粉末状の造滓剤(石灰石)を噴出させることに
より、溶鉄の酸化脱炭精錬を行っている。
And the refining gas flow path (inner pipe) of those tuyeres
In order to remove impurities such as phosphorus and sulfur along with oxidizing gas, powdered slag-forming agent (limestone) is jetted out to perform oxidation and decarburization of molten iron.

通常、LD転炉などの上吹き転炉の場合における脱硫反
応は、静的状態に近い溶融スラグと溶鉄との界面で、ス
ラグ中に溶解したCaOを脱硫剤として反応が進行する
Normally, in the case of a top-blown converter such as an LD converter, the desulfurization reaction proceeds at the interface between molten slag and molten iron in a nearly static state, using CaO dissolved in the slag as a desulfurization agent.

これに対し底吹き転炉では、炉底の羽目から粉末状の石
灰が未溶解固体状態で鋼浴中に供給されるため、CaO
の活性が前記LD転炉などの溶解したものの場合に比べ
るとかなり高い状態に置かれている。
On the other hand, in a bottom-blown converter, powdered lime is supplied into the steel bath in an undissolved solid state from the bottom lining of the furnace, so CaO
The activity is considerably higher than in the case of melted materials such as the LD converter.

しかも、その粉末状の石灰は、羽目直上で形成される多
数のガス気泡に付着したり、あるいは浴中に侵入分散す
るため、脱硫反応の界面積を著しく拡大するという利点
があり、脱硫は上吹き転炉に比べると底吹き転炉の方が
有利である。
Moreover, the powdered lime adheres to the numerous gas bubbles that form directly above the siding, or enters and disperses into the bath, which has the advantage of significantly expanding the interfacial area for the desulfurization reaction. A bottom-blown converter is more advantageous than a blown converter.

また、溶銑のS濃度が低い場合、浴中でのSの拡散が遅
くなるので、脱硫反応においてそれが律速段階となり、
脱硫速度が低下することが知られている。
In addition, when the S concentration in the hot metal is low, the diffusion of S in the bath becomes slow, which becomes the rate-limiting step in the desulfurization reaction.
It is known that the desulfurization rate decreases.

したがって、これを避けるためには、浴中を十分に撹拌
することが必要とされるが、底吹き転炉の場合にあって
は、炉底部に多数の羽目を有するため、浴中の溶鋼撹拌
強さが、上吹きランスに比べると極めて大きく、脱硫容
器として見た場合に有利である。
Therefore, in order to avoid this, it is necessary to stir the bath sufficiently, but in the case of a bottom-blowing converter, since there are many holes at the bottom of the furnace, the molten steel in the bath cannot be stirred. The strength is significantly greater than that of a top-blown lance, which is advantageous when viewed as a desulfurization vessel.

そこで、この発明は上述の知見にもとづき、低硫鋼を酸
素底吹き転炉によって溶製するという点に着目してなし
た方法である。
Therefore, the present invention is a method based on the above-mentioned knowledge, focusing on producing low sulfur steel using an oxygen bottom-blown converter.

しかしながら、従来の酸素底吹き転炉による精錬では、
焼石灰粉末を純酸素ガスとともに供給するのが普通であ
るから、たとえ脱硫上有利な炭素や珪素を多く含んだ(
溶銑段階にある)ものであるとしても、一旦生成したC
aSが再び酸化性ガスにより酸化されCaOを生成して
実質的には極低硫化は不可能であった。
However, in conventional refining using an oxygen bottom-blown converter,
Since burnt lime powder is usually supplied together with pure oxygen gas, even if it contains a lot of carbon or silicon, which is advantageous for desulfurization (
Even if it is in the hot metal stage), once it is generated,
aS was oxidized again by the oxidizing gas to produce CaO, making it virtually impossible to achieve extremely low sulfidation.

このことは次のように考えられる。This can be considered as follows.

すなわち、一般に、転炉内における脱硫反応は、次式;
%式% のように示される。
That is, in general, the desulfurization reaction in the converter is expressed by the following formula;
It is shown as % expression %.

このことから、溶鋼中の酸素濃度01あるいはそれらの
反応が起る場所の02分圧が高い場合には、スラグ中に
(CaS )として除去されたSが再びCaOに戻って
しまう欠点がある。
From this, when the oxygen concentration 01 in molten steel or the 02 partial pressure at the location where these reactions occur is high, there is a drawback that S, which was removed as (CaS) in the slag, returns to CaO.

そこで、発明者らは精錬中のある時期を特定し、そこで
強い脱硫吹錬を施すことにより、酸素分圧の低い脱硫に
好都合な条件をつくり、脱硫を促進するとともに、引続
き炉内を強還元雰囲気に維持して低硫鋼を溶製するよう
にしたのである。
Therefore, the inventors identified a certain period during refining and performed strong desulfurization blowing at that time, creating conditions favorable for desulfurization with low oxygen partial pressure, promoting desulfurization, and continuing to strongly reduce the inside of the furnace. This enabled the production of low-sulfur steel while maintaining the atmosphere.

要するに、この発明は、底吹き転炉を用い、かつ溶銑中
Sの活量が大きい二所謂はぼ溶銑状態である精錬初期に
、脱硫吹錬を実施して一旦低硫銑とする。
In short, this invention uses a bottom-blowing converter and performs desulfurization blowing at the early stage of refining when the hot metal is in the so-called molten metal state where the activity of S is high and is once made into low-sulfur pig iron.

その後引続いて炭素、珪素、燐、およびマンガンなどの
不純物を酸化除去し、しかもこの間一旦除去したSが再
び溶鋼中へ戻ることのないように吹錬を続けるようにし
た工業用純鉄の溶製方法である。
After that, impurities such as carbon, silicon, phosphorus, and manganese are removed by oxidation, and blowing is continued to prevent the S that has been removed from returning to the molten steel. This is the manufacturing method.

以下にその構成の詳細を実施例とともに説明する。The details of the configuration will be explained below along with examples.

この発明に係る溶製方法は次のような各過程から構成さ
れている。
The melting method according to the present invention is comprised of the following steps.

(イ)高炉から出銑した溶銑中のSを、あらかじめ炉外
脱硫装置によりo、oio%以下とし、温度を1200
℃を切らないよう保持する過程;(ロ)その炉外脱硫を
した溶銑から脱硫滓を分離する過程; (ハ)(0)で処理した溶銑を、炉底に精錬ガス通路と
冷却ガス通路とからなる複数の同心2重管羽口を具える
底吹き転炉内に装入し、酸素などの酸化性ガスを吹込み
、炭素濃度が3.5%以上、温度が1400℃以上の製
鋼ビートを形成させる過程; に)前記過程で示される製鋼ヒートが達成されたとき、
羽口の内管からは窒素またはアルゴンなどの不活性ガス
とともに、CaO粉末を吹込み、かつ外管からは炭化水
素系の還元ガスを吹込み、S含有量を0.002%以下
にする過程;(ホ)かかるに)の過程を経たのち、前記
羽口の内管から酸素などの精錬ガスを吹込み、脱炭、脱
燐、脱マンガン、および脱珪素反応を行なわせなから、
同時に羽口内管からCaO粉末を吹込み、溶鋼への復硫
を防止する過程; (へ)最後に出鋼する過程; つぎに、各過程について詳述する。
(b) The S content in the hot metal tapped from the blast furnace is reduced to 0.0% or less using an outside-furnace desulfurization device, and the temperature is set to 1200.
(b) Separating the desulfurization slag from the hot metal that has been desulfurized outside the furnace; (c) The hot metal treated in (0) is separated into a refining gas passage and a cooling gas passage at the bottom of the furnace. Steel beets are charged into a bottom blowing converter equipped with multiple concentric double tube tuyeres, and oxidizing gas such as oxygen is blown into them to produce steelmaking beets with a carbon concentration of 3.5% or more and a temperature of 1400°C or more. a) when the steelmaking heat shown in the above process is achieved,
A process in which CaO powder is injected together with an inert gas such as nitrogen or argon from the inner tube of the tuyere, and a hydrocarbon-based reducing gas is injected from the outer tube to reduce the S content to 0.002% or less. (e) After the process of (e)), a refining gas such as oxygen is blown into the inner pipe of the tuyere to cause decarburization, dephosphorization, demanganization, and desiliconization reactions.
At the same time, a process of injecting CaO powder from the inner tube of the tuyere to prevent resulfurization into the molten steel; (f) a process of finally tapping the steel; Next, each process will be described in detail.

まず、前記過程(イ)は、底吹き転炉内で0.002%
以下のS濃度を得るために必要な予備脱硫工程であり、
また溶銑の温度は1200℃より低下すると、後続の底
吹き転炉内での脱硫に支障をきたすため、この過程を終
了した時点で、溶銑温度は1200℃以上が必要である
First, in the process (a), 0.002%
This is a preliminary desulfurization step necessary to obtain the following S concentration,
Furthermore, if the temperature of the hot metal falls below 1200°C, it will interfere with the subsequent desulfurization in the bottom blowing converter, so the hot metal temperature needs to be at least 1200°C at the end of this process.

前記過程(0)は、脱硫滓が転炉内へ持ち込まれると、
精錬後期において、復硫の危険状があるために必要とな
る工程である。
In the step (0), when the desulfurization slag is brought into the converter,
This step is necessary because there is a danger of resulfurization in the latter stages of refining.

前記過程←→は、底吹き転炉内で溶銑の脱硫反応を有利
に展開するために、浴の温度を1400℃以上に昇熱す
る工程である。
The process ←→ is a step in which the temperature of the bath is raised to 1400° C. or higher in order to advantageously develop the desulfurization reaction of hot metal in the bottom blowing converter.

しかしこの際、溶銑中の炭素濃度が3.5%を切って下
がると還元性雰囲気下での脱硫の促進条件が弱まり、か
えって好ましくないので溶銑中の炭素濃度は3.5%以
上でなければならない。
However, at this time, if the carbon concentration in the hot metal drops below 3.5%, the conditions for promoting desulfurization in a reducing atmosphere will weaken, which is even unfavorable, so the carbon concentration in the hot metal must be 3.5% or higher. No.

前記過程に)は、脱硫反応に最も好ましい条件を整えて
、底吹き転炉内溶銑の脱硫を実施する工程であり、従来
の底吹き転炉吹錬法と異なり、不活性ガスで焼石灰粉末
を吹込みつつ、しかも羽目の外管からは炭化水素系の保
護ガスを吹込み、転炉内を強還元雰囲気となすものであ
り、こうして溶銑中のSをo、ooi%以下にすること
ができ、少なくとも0.002%以下に確実に脱硫する
ことが可能である。
The above process) is a process of desulfurizing the hot metal in the bottom blowing converter by arranging the most favorable conditions for the desulfurization reaction, and unlike the conventional bottom blowing converter blowing method, burnt lime powder is In addition, a hydrocarbon-based protective gas is blown into the converter from the outer tube of the siding to create a strongly reducing atmosphere inside the converter.In this way, it is possible to reduce the S content in the hot metal to less than o, ooi%. It is possible to reliably desulfurize to at least 0.002% or less.

前記過程ホ)は、当該溶銑中に含まれるS以外の不純物
、炭素、珪素、マンガン、および燐を除去し、工業用純
鉄を製造するための第2吹錬工程である。
The process e) is a second blowing step for removing impurities other than S, carbon, silicon, manganese, and phosphorus contained in the hot metal to produce industrial pure iron.

この際重要なことは、一旦スラグ中へ分離したSが、再
び炉内の強酸化性雰囲気によって、溶鉄中へ復硫する現
象を極力防止しなければならない。
What is important here is to prevent as much as possible the phenomenon in which S, once separated into the slag, resulfurizes into the molten iron due to the strongly oxidizing atmosphere in the furnace.

そのためにはここでの過程(ホ)にあっても、引き続き
焼石灰粉末を吹込むことが有利である。
For this purpose, it is advantageous to continue blowing in the burnt lime powder even during this step (e).

前記過程(へ)は、こうして溶製した工業用純鉄を取鍋
に出鋼する工程である。
The above step is a step of tapping the industrial pure iron produced in this way into a ladle.

なお、前記(ハ)の精錬の立上がり時の後、に)でいう
脱硫吹錬を実施する前に、珪素を添加することによって
、脱硫に有利な条件にしたのち、に)の脱硫吹錬を実施
する方が熱力学的にいうところのSの活量が増大して脱
硫反応を促進する上で有利であり、とくに底吹き転炉に
装入する前のSi濃度が低い場合に炉内でMnO,Fe
Oなとの低級酸化物が生成し、スラグとなって脱硫反応
を阻害するがSiを添加することにより、これらが再還
元され、脱硫反応に有利となるので、より効果が顕著に
なる。
In addition, after the start-up of the refining in (c) above, and before carrying out the desulfurization blowing referred to in (2), silicon is added to create favorable conditions for desulfurization, and then the desulfurization blowing in (2) is performed. It is thermodynamically more advantageous to increase the activity of S and promote the desulfurization reaction, especially when the Si concentration in the furnace is low before charging into the bottom blowing converter. MnO, Fe
Lower oxides such as O are generated and become slag, which inhibits the desulfurization reaction, but by adding Si, these are re-reduced and become advantageous to the desulfurization reaction, making the effect more pronounced.

また、復硫を抑えながら吹錬する精錬の中期から末期に
至る(ホ)の過程の後と、(へ)の過程(出鋼)に至る
中間に、Arガスなどの不活性ガスを羽口から炉内に吹
込むことにより該鋼浴を洗滌してから出鋼すると、H濃
度を0.0002%以下に、またO濃度を0.03%以
下とするのに効果がある。
In addition, inert gas such as Ar gas is injected into the tuyeres after the middle to final stage of refining (e), which involves blowing while suppressing resulfurization, and in the middle of the process (f) (e.g., tapping). Cleaning the steel bath by blowing it into the furnace before tapping is effective in reducing the H concentration to 0.0002% or less and the O concentration to 0.03% or less.

以下に、この発明の実施例について説明する。Examples of the present invention will be described below.

この実施例において使用した転炉は、5トンの酸素底吹
き転炉であり、羽口数は6本、内管を使った送酸速度2
3Nm/rmn、羽目冷却用に用いる外管から吹込むプ
ロパンガスの流量は0.69Nm’/minである。
The converter used in this example is a 5-ton oxygen bottom-blown converter with 6 tuyeres and an oxygen feed rate of 2 using inner tubes.
The flow rate of propane gas blown from the outer pipe used for cooling the siding was 0.69 Nm'/min.

実施例 1 まず60tの高炉溶銑を取鍋に保持し、その鍋内にカル
シウム・カーバイトを2.0 kg/ を添加しインペ
ラーを使って脱硫した。
Example 1 First, 60 tons of blast furnace hot metal was held in a ladle, and 2.0 kg/kg of calcium carbide was added to the ladle and desulfurized using an impeller.

その炉外脱硫後の溶銑を、6.90tの底吹き転炉用溶
銑鍋に分注した。
The hot metal after the outside-furnace desulfurization was dispensed into a 6.90 t hot metal ladle for a bottom blowing converter.

この時その溶銑鍋内の溶銑温度は1330’Cであり、
成分は4.48%C,0,88%Si、0.41%Mへ
0.110%P、0.007%Sであった。
At this time, the temperature of the hot metal in the hot metal pot was 1330'C,
The components were 4.48%C, 0.88%Si, 0.41%M, 0.110%P, and 0.007%S.

つぎに、かかる溶銑鍋の浴面にある滓を人力により掻き
出したのち、その脱硫溶銑を底吹き転炉に装入し、4分
30秒酸素吹精した。
Next, the slag on the bath surface of the hot metal pot was scraped out manually, and the desulfurized hot metal was charged into a bottom blowing converter and oxygen blown for 4 minutes and 30 seconds.

この吹精での送酸速度は23Nm1min1羽口冷却用
に外管に通すプロパン・ガス流量は0.69 N?71
3/ minであった。
The oxygen delivery rate in this blower is 23Nm/min, and the flow rate of propane gas passed through the outer pipe for cooling the tuyere is 0.69N? 71
It was 3/min.

この間、羽口内管からは焼石灰粉末を13kp/lヒー
ト吹込んだ。
During this time, burnt lime powder was heated at 13 kp/l through the tuyere inner tube.

ここで一旦倒炉して測温と分析を行ったところ、149
0’C,3,88%C,0,003%Si。
When we once collapsed the reactor and conducted temperature measurements and analysis, we found that the temperature was 149.
0'C, 3,88%C, 0,003%Si.

0.36%Mn 10.071%P、0.008%Sと
いう結果が得られた。
The results were 0.36%Mn, 10.071%P, and 0.008%S.

つづいて、羽口内管よりArガスを23 Nm’/m1
n1また羽口外管よりはプロパンガスを0.69 Nm
l minなる流量で流しつつ、2分55秒の脱硫吹錬
を実施し、同時に前記羽口内管からは25kg/lヒー
トの焼石灰粉末を吹込んだ。
Next, Ar gas was applied at 23 Nm'/m1 from the tuyere inner tube.
n1 Also, propane gas is 0.69 Nm from the tuyere outer tube.
Desulfurization blowing was carried out for 2 minutes and 55 seconds while flowing at a flow rate of 1 min, and at the same time, burnt lime powder of 25 kg/l heat was blown from the tuyere inner tube.

ここで倒炉し、鋼浴の温度と浴組成とを分析したところ
、1350°G、3.81%C,0,002%5i10
.36%Mn10.075%P10.001%Sであっ
た。
When the furnace was collapsed and the temperature and bath composition of the steel bath were analyzed, the results were 1350°G, 3.81%C, 0,002%5i10
.. It was 36%Mn10.075%P10.001%S.

その後、ひきつづき前記したところの吹錬条件、すなわ
ち羽口内管からの酸素ガス流量23Nm/m1n1およ
び羽口外管からのプロパンガス流量0.69 Nrl/
minにて通常の脱炭吹錬を16分OO秒行った。
Thereafter, the blowing conditions as described above were continued, that is, the oxygen gas flow rate from the tuyere inner pipe was 23 Nm/m1n1, and the propane gas flow rate from the tuyere outer pipe was 0.69 Nrl/
Normal decarburization blowing was performed at min for 16 minutes OO seconds.

この間40k19/lヒートの焼石灰粉末を羽口内管よ
り吹込んだ。
During this time, burnt lime powder with a heat of 40k19/l was blown into the tuyere tube.

倒炉して測温と分析を行ったところ、1710℃、0.
008%C,0,002%5i10、O35Mn、0.
005%P10.0020%S、0.072%0であっ
た。
When the furnace was collapsed and the temperature was measured and analyzed, it was found to be 1710℃ and 0.5℃.
008%C, 0,002%5i10, O35Mn, 0.
005%P10.0020%S, 0.072%0.

最後に、受鋼取鍋に3kgのMを入れて直ちに出鋼し、
その受鋼取鍋から6tの上広鋳型に1600℃の温度で
上注した。
Finally, put 3 kg of M into the receiving ladle and tap the steel immediately.
The steel was poured from the ladle into a 6-ton wide mold at a temperature of 1600°C.

鋼塊のチェック分析によれば、o、oos%C,0,0
03%Si、0.032%M n 。
According to the check analysis of the steel ingot, o,oos%C,0,0
03%Si, 0.032%Mn.

0.007%P、0.0020%S、0.0014%N
10.0040%H,0,03%0,0.001%A7
なる工業用純鉄が得られた。
0.007%P, 0.0020%S, 0.0014%N
10.0040%H, 0.03%0, 0.001%A7
Industrial pure iron was obtained.

実施例 ■ まず60tの高炉溶銑を取鍋に保持し、その鍋内にカル
シウム・カーバイトを1.8kg/を添加しインペラー
を使って脱硫した。
Example 1 First, 60 tons of blast furnace hot metal was held in a ladle, and 1.8 kg of calcium carbide was added to the ladle and desulfurized using an impeller.

その炉外脱硫後の溶銑を6.8を底吹き転炉用溶銑鍋に
分注した。
After the outside-furnace desulfurization, 6.8 liters of the hot metal was dispensed into a hot metal ladle for a bottom blowing converter.

この時該溶銑鍋内の溶銑温度は1260’Cであり、成
分は4.45%C,0,64%5i10.52%庵、0
.12%P、0.009%Sであった。
At this time, the hot metal temperature in the hot metal pot was 1260'C, and the components were 4.45%C, 0.64%5i, 10.52%an, 0
.. It was 12% P and 0.009% S.

つぎに、かかる溶銑鍋の浴面にある滓を入力により掻き
出したのち、その溶銑を底吹き転炉内に装入し、4分5
秒間酸素吹錬を実施した。
Next, the slag on the bath surface of the hot metal pot is scraped out by input, and then the hot metal is charged into the bottom blowing converter, and the slag is poured into the bottom blowing converter for 4 minutes and 5 minutes.
Oxygen blowing was performed for seconds.

この時期での羽口内管から吹込んだ焼石灰は13.7k
g/lヒートであり、また鋼浴温度は1458℃、浴の
成分は3.6%C,0,003%Si、0.35%Mn
、 0.112%P10.009%Sであった。
The amount of burnt lime injected from the tuyere tube at this time was 13.7k.
g/l heat, the steel bath temperature was 1458°C, and the bath composition was 3.6%C, 0,003%Si, 0.35%Mn.
, 0.112%P10.009%S.

この時期を経過したのち、次の工程に入る前に金属Si
を6kg/lヒート炉内に添加した。
After this period, the metal Si
was added to the heat furnace at 6 kg/l.

つづいて、2重管羽口上の内管よりArガスを23 N
mlmin 、また羽口外管よりはプロパンガスを0.
69 Nm37 minなる流量で流しツツ、4分5秒
の吹錬を実施し、この間羽口内管から25kIi/lヒ
ートの焼石灰粉末を吹込んだ。
Next, 23N of Ar gas was applied from the inner tube above the double tube tuyere.
mlmin, and 0.0% propane gas from the tuyere outer tube.
Blowing was carried out for 4 minutes and 5 seconds at a flow rate of 69 Nm37 min, during which time burnt lime powder at a heat of 25 kIi/l was blown from the tuyere inner tube.

ここで直ちに倒炉して鋼浴の温度と組成を分析をしたと
ころ、1345℃、3.56%C10,55%Si、
0.35%Mn。
When the furnace was immediately collapsed and the temperature and composition of the steel bath was analyzed, the temperature was 1345℃, 3.56%C10, 55%Si,
0.35%Mn.

0.112%P、0.001%Sであった。It was 0.112% P and 0.001% S.

その後、ひきつづき前記したところの吹錬条件、すなわ
ち羽口内管からの酸素ガス流量23Nm’/m1n1お
よび羽口外管からのプロパンガス流量0.69Nm’/
minにて、通常の脱炭吹錬を、12分19秒行った。
Thereafter, the blowing conditions described above were continued, that is, the oxygen gas flow rate from the tuyere inner pipe was 23 Nm'/m1n1, and the propane gas flow rate from the tuyere outer pipe was 0.69 Nm'/m1n1.
Normal decarburization blowing was performed at min. for 12 minutes and 19 seconds.

この間40kg/lヒートの焼石灰粉末を、羽口内管よ
り吹込んだ。
During this time, 40 kg/l heat of burnt lime powder was blown into the tuyere tube.

再び、倒炉して測温と分析を行ったところ、1750℃
、0.009%C10,002%Si、0.04%Mn
、 0.007%八へ、001%S、0.06%Oであ
った。
When the furnace was collapsed again and the temperature was measured and analyzed, it was found to be 1750℃.
, 0.009%C10,002%Si, 0.04%Mn
, 0.007% H8, 001% S, and 0.06% O.

最後に受鋼取鍋に3kgのAlを入れて直ちに出鋼し、
その受鋼取鍋から6tの上広鋳型に、1620℃の温度
で上注した。
Finally, put 3 kg of Al into the receiving ladle and tap the steel immediately.
The steel was poured from the ladle into a 6-ton wide mold at a temperature of 1620°C.

鋼塊のチェック分析によれば、o、oos%C,0,0
03%Si。
According to the check analysis of the steel ingot, o,oos%C,0,0
03%Si.

0.043%Mn、 0.009P、 0.0010
%810.0017%N、0.00038%H,0,0
2%o10.002%Alなる工業用純鉄が得られた。
0.043%Mn, 0.009P, 0.0010
%810.0017%N, 0.00038%H, 0,0
Industrial pure iron of 2% o 10.002% Al was obtained.

実施例 ■ この実施例に当って使用した転炉は、先の実施例Iのも
のと同じ5を酸素底吹き転炉である。
Example 2 The converter used in this example was the same 5 oxygen bottom-blown converter as in Example I above.

前述のようにして脱硫処理をした後、底吹き転炉用溶銑
鍋に、重量が6.72t、温度が1306℃、成分が4
.36%C10,79%5i10.39%Mn10.1
26%P、0.008%Sの溶銑を受銑した。
After desulfurization treatment as described above, hot metal of 6.72 tons in weight, 1306°C in temperature, and 4 in composition was placed in the bottom blowing converter ladle.
.. 36%C10, 79%5i10.39%Mn10.1
Hot metal containing 26% P and 0.008% S was received.

溶銑鍋浴面のスラグを掻き取って除去した後、その脱硫
溶銑を底吹き転炉に装入し、4分05秒酸素吹錬した。
After scraping and removing the slag on the surface of the hot metal pot bath, the desulfurized hot metal was charged into a bottom blowing converter and oxygen blown for 4 minutes and 05 seconds.

この吹錬での送酸速度は23Nm’/min、羽ロ冷却
用に外管に通すプロパンガス流量は、0.69 Nrr
l/ minであった。
The oxygen supply rate in this blowing was 23 Nm'/min, and the flow rate of propane gas passed through the outer pipe for cooling the blade was 0.69 Nrr.
l/min.

この間羽口内管からは焼石灰粉末を、13kg/lヒー
ト吹き込んだ。
During this time, 13 kg/l of burnt lime powder was heated and blown into the tuyere tube.

ここで一旦倒炉して測温と分析を行ったところ、148
0℃、3.73%C10,003%Si。
When we once collapsed the reactor and conducted temperature measurements and analysis, we found that 148.
0°C, 3.73%C10,003%Si.

0.22%Mn、 0.093%P10.008%Sと
いう結果が得られた。
The results were 0.22%Mn, 0.093%P10.008%S.

つづいて、羽口内管よりArガスを23 N m”/
min 1また羽口外管よりはプロパンガスを0.69
Nrrt/ minなる流量で流しつつ、3分12秒
の脱硫吹錬を実施し、同時に前記羽口内管から25kg
/lヒートの焼石灰粉末を吹込んだ。
Next, Ar gas was applied at 23 N m”/
min 1 Also, from the tuyere outer pipe, propane gas is 0.69
While flowing at a flow rate of Nrrt/min, desulfurization blowing was carried out for 3 minutes and 12 seconds, and at the same time 25 kg was removed from the tuyere inner pipe.
/l heat of burnt lime powder was injected.

ここで倒炉して鋼浴の温度と浴組成とを分析したところ
、1342℃、3.77%C,0,003%Si。
When the furnace was collapsed and the temperature and bath composition of the steel bath were analyzed, it was found to be 1342°C, 3.77%C, 0,003%Si.

0.22%Mn、0.102%P、0.001%Sであ
った。
The content was 0.22% Mn, 0.102% P, and 0.001% S.

その後前記したところの吹錬条件、すなわち、羽口内管
からの酸素ガス流量23 Nm’/min、および羽口
外管からのプロパンガス流量0.69Nm”/minに
て、脱炭吹錬を15分18秒行った。
Thereafter, decarburization blowing was performed for 15 minutes under the blowing conditions described above, that is, an oxygen gas flow rate of 23 Nm'/min from the tuyere inner tube and a propane gas flow rate of 0.69 Nm''/min from the tuyere outer tube. It took 18 seconds.

この間27 ky/ tヒートの焼石灰粉末を羽口内管
より吹込んだ。
During this time, burnt lime powder at a heat rate of 27 ky/t was blown into the tuyere tube.

再び倒炉して浴温と浴の組成を分析したところ、170
6℃、0.010C,0,002%Si、0.043%
Mn、0.006%P10.0018%810.074
%Oであった。
When we collapsed the furnace again and analyzed the bath temperature and bath composition, we found that 170
6℃, 0.010C, 0.002%Si, 0.043%
Mn, 0.006%P10.0018%810.074
%O.

その後、羽口内管に20 N77L’/ mi nのA
rガスを流し、羽口外管にも0.8 Nm’/minの
Arガスを流し、3分間吹精した後直ちに3kgの金属
Mを入れた受鋼取鍋中に出鋼し、またその取鍋からは6
tの上広鋳型に1580℃の温度で上注した。
After that, 20 N77L'/min of A was applied to the tuyere inner tube.
After flowing r gas and flowing Ar gas at a rate of 0.8 Nm'/min into the tuyere outer tube, the steel was blown for 3 minutes and then immediately tapped into a receiving ladle containing 3 kg of metal M. 6 from the pot
The mixture was poured into a top mold at a temperature of 1580°C.

当該鋼塊のチェック分析によれば、0.006%C10
,002%5ls0.03%Mn10.OO6%P10
.0017%s1o、ooio%N10.0021%H
10,017%0.0.001%Alなる工業用純鉄が
得られた。
According to the check analysis of the steel ingot, 0.006% C10
,002%5ls0.03%Mn10. OO6%P10
.. 0017%s1o, ooio%N10.0021%H
Industrial pure iron containing 10,017% and 0.0.001% Al was obtained.

なお、上述した実施例では5tの小型炉を使用したため
熱損失が大きく、工業用純鉄の製造に支障のない片材(
珪素鋼スクラップなど)の炉内装入は不必要であった。
In addition, in the above-mentioned example, a small furnace of 5 tons was used, so the heat loss was large, and the single piece material (
It was unnecessary to introduce silicon steel scrap, etc.) into the furnace.

しかし、100tを越える大型炉などにおいては、熱収
支上から片材装入が必要となることがありその場合、片
材を装入してもよい。
However, in large furnaces exceeding 100 tons, it may be necessary to charge pieces of material from the viewpoint of heat balance, and in that case, pieces of material may be charged.

以上説明したように、この発明によれば比較的簡便に工
業用純鉄の製造が可能である。
As explained above, according to the present invention, industrial pure iron can be produced relatively easily.

Claims (1)

【特許請求の範囲】 1 予め炉外で脱硫をしかつその予備脱硫によって生成
した脱硫滓を除去してなるS:0.010%以下の脱硫
溶銑から、炉底に精錬用ガス通路と保護ガス用通路とか
らなる2重管羽目を有する底吹き転炉により工業用純鉄
を溶製するに当り、(イ)上記脱硫溶銑を、該底吹き転
炉内に装入し、羽目から酸素などの酸化性ガスを噴射し
て吹錬し、Cが3.5%以上、温度が1400’C以上
の製鋼ヒートを形成させ、 (ロ)その後、前記羽目の精錬ガス通路から不活性ガス
とともに粉末焼石灰を噴射し、かつ保護ガス用通路から
は還元性ガスを噴射して吹錬し、Sを0.002%以下
にもち来たし、 (ハ)その後もさらに前記精錬用ガス通路から焼石灰粉
末を混入させた酸素ガスを噴射しつづけて酸化脱炭吹錬
を行い、 に)しかる後に出鋼を行なう、 ことからなる底吹き転炉による工業用純鉄の溶製方法。 2 予め炉外で脱硫をしかつその予備脱硫によって生成
した脱硫滓を除去してなるS:0.010%以下の脱硫
溶銑から、炉底に精錬用ガス通路と保護ガス用通路とか
らなる2重管羽目を有する底吹き転炉により工業用純鉄
を溶製するに当り、(イ)上記脱硫溶銑を、該底吹き転
炉内に装入し、羽目から酸素などの酸化性ガスを噴射し
て吹錬し、Cが3.5%以上、温度が1400℃以上の
製鋼ヒートを形成させ、 (ロ)つぎに、その浴中に金属Siを投入し、(ハ)そ
の後、前記羽口の精錬ガス通路から不活性ガスとともに
粉末焼石灰を噴射し、かつ保護ガス通路からは還元性ガ
スを噴射して吹錬し、Sを0.002%以下にもち来た
し、 に)その後もさらに前記精錬用ガス通路から焼石灰粉末
を混入させた酸素ガスを噴射しつづけて酸化脱炭吹錬を
行い、 (ホ)しかる後に出鋼を行なう、 ことからなる底吹き転炉による工業用純鉄の溶製方法。 3 予め炉外で脱硫をしかつその予備脱硫によって生成
した脱硫滓を除去してなるS:0.010%以下の脱硫
溶銑から、炉底に精錬用ガス通路と保護ガス用通路とか
らなる2重管羽目を有する底吹き転炉により工業用純鉄
を溶製するに当り、げ)上記脱硫溶銑を、該底吹き転炉
内に装入し、羽目から酸素などの酸化性ガスを噴射して
吹錬し、Cが3.5%以上温度が1400℃以上の製鋼
ヒートを形成させ、 (ロ)つぎに、その浴中に金属Siを投入し、(ハ)そ
の後、前記羽目の精錬ガス通路から不活性ガスとともに
粉末焼石灰を噴射し、かつ保護ガス通路からは還元ガス
を噴射して吹錬し、SをQ、002%以下にもち来たし
、 に)その後もさらに前記精錬用ガス通路から焼石灰粉末
を混入させた酸素ガスを噴射しつづけて酸化脱炭吹錬を
行い、 (ホ)しかる後に、前記羽口から不活性ガスを噴射して
酸素ガス等の脱ガスを行い、 (へ)そして出鋼する、 ことからなる底吹き転炉による工業用純鉄の溶製方法。
[Claims] 1. From desulfurized hot metal with S: 0.010% or less, which is obtained by desulfurizing in advance outside the furnace and removing the desulfurization slag generated by the preliminary desulfurization, a refining gas passage and a protective gas are added to the bottom of the furnace. When melting industrial pure iron using a bottom-blown converter having a double-pipe siding consisting of a pipe passage, (a) the above-mentioned desulfurized hot metal is charged into the bottom-blowing converter, and oxygen, etc. oxidizing gas is injected to form a steelmaking heat with a C content of 3.5% or more and a temperature of 1400'C or more; Burnt lime was injected and reducing gas was injected from the protective gas passage for blowing to bring S to 0.002% or less, and (c) After that, burned lime powder was further injected from the refining gas passage. A method for producing pure iron for industrial use using a bottom-blowing converter, which consists of continuously injecting oxygen gas mixed with iron to perform oxidative decarburization blowing, and (2) subsequently tapping the steel. 2. From desulfurized hot metal with S: 0.010% or less, which is obtained by desulfurizing in advance outside the furnace and removing the desulfurization slag generated by the preliminary desulfurization, 2 consists of a refining gas passage and a protective gas passage at the bottom of the furnace. When melting industrial pure iron using a bottom-blown converter having heavy pipe linings, (a) the above-mentioned desulfurized hot metal is charged into the bottom-blowing converter, and oxidizing gas such as oxygen is injected through the linings. and blowing to form a steelmaking heat with a carbon content of 3.5% or more and a temperature of 1400°C or higher, (b) next, metal Si is introduced into the bath, (c) then the tuyere Powdered calcined lime was injected together with an inert gas from the refining gas passage, and reducing gas was injected from the protective gas passage for blowing to bring the S content to 0.002% or less. Production of industrial pure iron using a bottom blowing converter, which consists of continuously injecting oxygen gas mixed with burnt lime powder from the refining gas passage to carry out oxidation and decarburization blowing, and (e) then tapping the steel. Melting method. 3 Desulfurization is done in advance outside the furnace and the desulfurization slag generated by the preliminary desulfurization is removed.S: 0.010% or less desulfurized hot metal is made of desulfurized hot metal with a refining gas passage and a protective gas passage at the bottom of the furnace.2 When melting industrial pure iron using a bottom-blown converter having heavy pipe linings, the above-mentioned desulfurized hot metal is charged into the bottom-blowing converter, and oxidizing gas such as oxygen is injected through the linings. (b) Next, metal Si is introduced into the bath, (c) After that, the refining gas of the above-mentioned size is heated. Powdered burnt lime was injected together with inert gas from the passage, and reducing gas was injected from the protective gas passage for blowing to bring S to Q,002% or less. Oxidative and decarburizing blowing is carried out by continuously injecting oxygen gas mixed with burnt lime powder from the tuyere, (e) After that, inert gas is injected from the tuyere to degas oxygen gas, etc. A method for producing industrial pure iron using a bottom blowing converter, which comprises:
JP53101866A 1978-08-23 1978-08-23 Method for producing industrial pure iron using a bottom blowing converter Expired JPS5833289B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP53101866A JPS5833289B2 (en) 1978-08-23 1978-08-23 Method for producing industrial pure iron using a bottom blowing converter

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP53101866A JPS5833289B2 (en) 1978-08-23 1978-08-23 Method for producing industrial pure iron using a bottom blowing converter

Publications (2)

Publication Number Publication Date
JPS5528372A JPS5528372A (en) 1980-02-28
JPS5833289B2 true JPS5833289B2 (en) 1983-07-19

Family

ID=14311908

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (1)

Country Link
JP (1) JPS5833289B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH067860Y2 (en) * 1987-01-28 1994-03-02 大見工業株式会社 Cutting tool

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5219525B2 (en) * 1972-09-05 1977-05-28
SE7501446L (en) * 1974-02-11 1975-08-12 Uss Eng & Consult
US3985550A (en) * 1975-01-23 1976-10-12 United States Steel Corporation Method of producing low sulfur steel
JPS5837366B2 (en) * 1976-04-16 1983-08-16 日本鋼管株式会社 Pretreatment method for molten metal

Also Published As

Publication number Publication date
JPS5528372A (en) 1980-02-28

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