JPS6315325B2 - - Google Patents
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- Publication number
- JPS6315325B2 JPS6315325B2 JP13282183A JP13282183A JPS6315325B2 JP S6315325 B2 JPS6315325 B2 JP S6315325B2 JP 13282183 A JP13282183 A JP 13282183A JP 13282183 A JP13282183 A JP 13282183A JP S6315325 B2 JPS6315325 B2 JP S6315325B2
- Authority
- JP
- Japan
- Prior art keywords
- hot metal
- refining
- tank
- melting
- blowing
- 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
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21C—PROCESSING OF PIG-IRON, e.g. REFINING, MANUFACTURE OF WROUGHT-IRON OR STEEL; TREATMENT IN MOLTEN STATE OF FERROUS ALLOYS
- C21C5/00—Manufacture of carbon-steel, e.g. plain mild steel, medium carbon steel or cast steel or stainless steel
- C21C5/28—Manufacture of steel in the converter
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P10/00—Technologies related to metal processing
- Y02P10/20—Recycling
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- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Refinement Of Pig-Iron, Manufacture Of Cast Iron, And Steel Manufacture Other Than In Revolving Furnaces (AREA)
Description
本発明は溶銑の加炭溶解精錬方法に関する。
現在の精鉄法の主流を占める高炉−転炉法は、
鉄精錬、溶解に必要な熱量を、溶銑のC、Si等の
酸化反応熱と溶銑自体の顕熱に依存しているた
め、一般にはスクラツプ消化能力は20〜30%であ
り、70%〜80%の溶銑を主体として使用せざるを
得ない。又鉄鉱石を転炉精錬中に添加して鉄を還
元回収する方法は、極めて合理的な鉄還元法であ
るが吸熱が多く、一般的転炉精錬では、鋼t当り
10Kg〜40Kg程度の鉄鉱石しか使用出来ない状況に
ある。
この様に溶銑を主原料とする転炉精錬法は、熱
的問題からスクラツプの多消費が不可能である事
と、最も合理的な鉄鉱石還元を、多量の鉄鉱石を
添加して実施する事が不可能である。
これらの難点を解決するため、転炉精錬中に炭
素物質(コークス、石炭)等を熱源として添加し
て、転炉の熱的裕度を向上させる各種の方法が提
案されているが、これらの方式は、下記の理由か
ら、転炉の熱的裕度をスクラツプ消費量にして、
たかだか3〜7%程度向上させるにすぎなかつ
た。
(1) コークス、石炭等の加炭物質が含有している
灰分が多く、転炉の様な単一容器では、スラグ
が激増し加炭量の限界がある。
(2) 一般の転炉脱炭精錬での脱炭反応は、主にC
+1/202→COであり、C+O2→CO2の反応に
比較すると、発熱量が約1/3と低く、多量の炭
素物質を転炉に添加せざるを得ない。その場合
当然(1)の問題点が発生する以外に、多量の高温
COガスが排ガスとして発生し、炉内の熱をも
ちさる結果となり、経済的な意味からこの方式
は成立しないものになつている。
本発明は、上吹酸素ガスによる脱炭精錬で最も
発熱量の多い反応を得て、炉内熱効率の最善化を
図る溶銑の加炭溶解精錬方法を提供するものであ
る。
更に本発明は、上吹酸素ガスによる精錬時に加
炭によつて溶銑に熱源を加え、投入屑鉄、鉄鉱石
の効率的な溶解精錬方法を提供するものである。
以下本発明を詳細に説明する。
上吹酸素を主体とする溶銑での加炭脱炭溶解精
錬における熱効率向上の要素技術を検討の結果、
以下の事実が明らかとなつた。溶銑の酸素精錬時
に溶銑中の炭素が、C+O2→CO2反応を起こす事
が熱効率改善の基本になるわけであるが、これを
得るための必要条件を調査した結果、底吹きを伴
う酸素精錬時の酸素吹錬条件と排ガス中CO/
CO2+COの関係は、第2図に示す様に、火点面
積/浴表面積比と、溶銑浴深さ/溶銑浴内径比と
極めて強い関係を持ち火点面積比が大きい程浴深
さが深い程C+O2→CO2の反応はよく起り、火点
面積/浴表面積が0.5近傍及び浴深さ/浴内径が
0.5近傍に臨界点があることが明らかである。な
お溶銑浴内径が円形でない場合は円形換算面積相
当内径とする。
上記火点面積/浴表面積は、次に説明する脱炭
精錬時の溶銑温度とも密な関係を有する。
ここに火点面積/浴表面積とは第1図に示すよ
うに、酸素ガス吹精時にランス孔から噴射され、
浴表面に幾何学に投影される面積Sが浴表面積
Lsに占める比率を指称する。
次に溶銑温度と排ガスCO/CO2+COの関係
が、第3図に示す如く、脱炭精錬時の溶銑温度が
1500℃以下では急激にCO/CO2+CO比が低下
し、1500℃に臨界点があることが明らかである。
図は火点面積/浴表面積=0.65、スラグ量10Kg/
tにおけるものであるが、実験によると火点面
積/浴表面積を0.3以上に保持しつつ溶銑温度を
1500℃以下に制御するときCO/CO2+CO比の減
少が確認された。
更に炉内スラグ量と排ガス中CO/CO2+COの
関係は、第4図に示す様に溶銑の上吹酸素による
脱炭中の炉内の溶銑t当りのスラグ量と、排ガス
中CO/CO2+COの関係は、スラグ量が15Kg/t
以上になると急激に上昇することが明らかであ
る。図における火点面積/浴表面積は0.6である。
以上の要素条件の検討の結果、加炭溶解精錬法
において、最も効率的に上吹酸素ガスによる脱炭
反応で、積極的にC+O2→CO2の最も発熱量の多
い反応を起こさせ、炉内熱効率の最善化を計る手
段は酸素ガス脱炭精錬時の火点面積/浴面積>
0.5及び浴深さ/浴内径≧0.5に保持することであ
る。なお溶銑温度を1500℃以下に保持するとき
は、この値はそれぞれ0.3まで拡大できる。
更に本発明によると、火点面積/浴表面積の条
件とともに、酸素ガス脱炭精錬時の溶銑温度を、
1500℃以下に保持することが望ましく、酸素ガス
脱炭精錬中のスラグ量を、15Kg/t以下に制御す
る要素技術を更につけ加える時は最も効率的であ
ることを確認した。
次に本発明の加炭溶解精錬方法の適用例につい
て説明する。
第5図は本発明の装置を示す。図において加炭
槽10は排滓孔12、底吹撹拌ガス孔14、加炭
剤インジエクシヨン11、屑鉄、鉄鉱石投入装置
23を有し、脱炭溶解精錬槽21との境界に分離
壁13を設ける。分離壁13は、溶銑上部域にお
いて、加炭槽10と脱炭溶解精錬槽21とを分離
し、槽の底部において溶湯の流路を形成する。
脱炭溶解精錬槽21は酸素ガスランス22、出
鋼孔24、底吹撹拌ガス孔25を有し分離壁の導
通域に近く電磁撹拌装置26を設ける。
本発明によると、2槽からなる溶解精錬炉に少
量の溶銑を装入(又はあらかじめ炉内に残してお
く)した後、加炭槽では底吹撹拌ガスを吹込みな
がら、加炭剤を上部より適時装入又はインジエク
シヨン法により溶銑に添加する。ある程度以上ス
ラグが生成すると、排滓孔より自然排滓するか又
は強制的にスラグクリーナー等で排滓する。
一方脱炭溶解精錬槽では、溶銑浴深さ(m)/
溶銑浴内径(m)が0.5以上に維持され、火点面
積/浴表面積≧0.50になる様上吹酸素を吹き、且
つ底吹きガスを吹き込み撹拌を強化しながら脱炭
精錬を続ける。又少なくとも加炭槽で加炭が実施
されている間は、溶銑温度が1500℃以上にならな
い様に、スクラツプ又は鉄鉱石等の酸化物質を上
部より添加する。又必要によつては、石灰、螢石
等の精錬剤を添加する。実験によると溶銑温度を
1500℃以下に制御するときはL/D及びS/Ls
は0.3以上で差し支えない。必要量の加炭溶解の
後、溶銑をはらい出す事も出来るし、又引続き脱
炭精錬をつづけ、必要な溶鋼温度、炭素量になつ
た所で出鋼してもよい。
尚、脱炭溶解精錬槽と加炭槽の分離壁は、少な
くとも精錬槽と加炭槽の溶銑が、溶銑下部層にお
いて相互に混合出来ればよいものであつて、主た
る目的は、前述した如く加炭槽のスラグが精錬槽
に流入するのを防止するものである。
以上を実施する事によつて、極めて熱効率良く
多量のスクラツプ消化が可能となり、又多量の鉄
鉱石等の酸化物の還元が可能となつた。
第6図は本発明の他の適用例の説明図である。
加炭槽10及び脱炭溶解精錬槽21は、第5図
と同様であるので説明を省略するが、本例では分
離壁13−1及び13−2を設けて3槽とし、脱
硫槽31に脱硫剤インジエクシヨン槽32を配設
し、底吹撹拌ガス吹込孔14−2を有する。本例
は脱硫槽を追加するものであるが、脱硫方法は、
脱硫剤を上方に装入して、底部よりガス撹拌して
実施する事も出来るし、又インジエクシヨンラン
スで吹き込む事も可能である。
各反応槽のスラグが脱炭槽に混入するのを防止
する方法として、前述した様に一つの容器内で各
槽の溶銑を、上部で分離する方法の他に、各反応
槽を別個の独立した容器として、各容器間を電磁
力移送法、真空吸上げ移送法等で結合し、相互の
溶銑を移送混合する事も可能である。
第7図イは本発明の更に他の適用例を平面図で
示す。
脱炭溶解精錬槽21、加炭槽10、脱硫槽3
1、が併設され、分離壁13−1,13−2で導
通口を設けて、分離された箱型3槽分離型溶解精
錬炉である。27は真空スラグクリーナ、19は
溶銑移送孔(第7図ロ)を示す。
即ち本例によれば、第1槽21では上部より酸
素ガスをランス22で吹精し、底部から撹拌ガス
を吹込み、鉄鉱石投入装置21を用いて溶解精錬
を行う。粗溶鋼を第2槽10に導入し、石炭粉を
上吹ランス11で噴入し、発生スラグを排滓孔1
2で排出する。第3槽31で、脱硫剤インジエク
シヨン32を用いて脱硫後第1層21に戻し、連
続操業を行うことができる。
第8図は本発明の更に他の適用例を示す模式図
である。
図において加炭槽10、脱炭溶解精錬槽21及
び脱硫槽31は、それぞれ通路36で導通され、
電磁移送器35により溶湯の移送を行う。加炭槽
10にスラグオフ12を、又脱硫(脱燐)槽31
にスラグオフ33を設け、脱炭溶精錬槽21から
溶鋼を取鍋27に出鋼する。
以上本発明を主として分離型連続炉に適用した
例について説明したが、勿論本発明の目的に反し
ない限り、バツチ型式の単独炉で操業することも
本発明の範囲を逸脱するものではない。
本発明は上述の通り溶銑の加炭溶解精錬を行う
に当り、炉底に撹拌ガス底吹孔を設け、分離壁に
より溶銑上層域を分離して、少くとも2槽以上に
構成して、加炭槽と脱炭溶解精錬槽を形成し、必
要により3槽として脱硫槽を併設したので、酸素
ガス上吹精錬において、多量の鉄鉱石、屑鉄の副
原料を、石炭添加の併用によつて加炭溶解精錬を
可能にして、その工業的効果は大である。
実施例 1
180tの酸素上吹、Arガス底吹の複合精錬炉に
おいて浴径L3.2m、浴深D3.2m(L/D=1.0、以
下L/Dとする)で酸素上吹ランスからの鋼浴表
面上での火点面積(鋼浴表面に対する酸素ガスの
衝突全面積≒N×(R+l・tanQ)2×π
N=ランスノズル数
R=ランス孔半径
l=ランス高さ
Q=ノズルスロート角度
が5.6m2(火点面積率0.7)になるようにランス高
さを調整し、第1表に示す様に、炉内でのC+
O2→CO2の反応を積極的におこなわせ、多量のス
クラツプを溶解し、鋼を精錬することが出来た。
The present invention relates to a method for carburizing, melting, and refining hot metal. The blast furnace-converter method, which currently dominates the iron refining process,
The amount of heat required for iron smelting and melting depends on the oxidation reaction heat of C, Si, etc. in the hot metal and the sensible heat of the hot metal itself, so the scrap digestion capacity is generally 20-30%, and 70%-80%. % of hot metal must be used as the main ingredient. In addition, the method of reducing and recovering iron by adding iron ore during converter refining is an extremely rational iron reduction method, but it absorbs a lot of heat, and in general converter refining, the
Currently, only iron ore weighing between 10Kg and 40Kg can be used. In this way, the converter refining method, which uses hot metal as the main raw material, cannot consume a large amount of scrap due to thermal problems, and the most rational iron ore reduction is carried out by adding a large amount of iron ore. things are impossible. In order to solve these difficulties, various methods have been proposed to improve the thermal margin of the converter by adding carbon materials (coke, coal), etc. as a heat source during converter refining. The method uses the thermal margin of the converter as the scrap consumption for the following reasons.
The improvement was only about 3 to 7% at most. (1) Carburizing substances such as coke and coal contain a large amount of ash, and in a single container like a converter, slag increases dramatically, and there is a limit to the amount of carburizing. (2) The decarburization reaction in general converter decarburization refining is mainly caused by C
+1/20 2 →CO, the calorific value is about 1/3 lower than the reaction of C+O 2 →CO 2 , and a large amount of carbon material must be added to the converter. In that case, in addition to the problem (1) naturally occurring, a large amount of high temperature
CO gas is generated as exhaust gas and takes away the heat inside the furnace, making this method unviable from an economical point of view. The present invention provides a method for carburizing, melting and refining hot metal, which achieves the reaction with the highest calorific value in decarburization refining using top-blown oxygen gas, and optimizes the thermal efficiency in the furnace. Furthermore, the present invention provides an efficient method for melting and refining input scrap iron and iron ore by adding a heat source to hot metal through carburization during refining using top-blown oxygen gas. The present invention will be explained in detail below. As a result of examining elemental technologies for improving thermal efficiency in carburization, decarburization, melting and refining using hot metal mainly using top-blown oxygen, we found that:
The following facts have become clear. The basis for improving thermal efficiency is that the carbon in the hot metal undergoes a C+O 2 → CO 2 reaction during oxygen refining of the hot metal.As a result of investigating the necessary conditions to achieve this, we found that oxygen refining with bottom blowing Oxygen blowing conditions and CO in exhaust gas at
As shown in Figure 2, the relationship between CO 2 + CO is extremely strong with the hot spot area/bath surface area ratio and hot metal bath depth/hot metal bath inner diameter ratio; the larger the hot metal bath area ratio, the deeper the bath depth. The reaction C + O 2 → CO 2 occurs frequently, and when the fire spot area/bath surface area is around 0.5 and the bath depth/bath inner diameter is around 0.5,
It is clear that there is a critical point near 0.5. If the inner diameter of the hot metal bath is not circular, use the inner diameter equivalent to the circular area. The above hot spot area/bath surface area has a close relationship with the hot metal temperature during decarburization refining, which will be explained next. Here, the flash point area/bath surface area means, as shown in Figure 1, when oxygen gas is ejaculated, it is injected from the lance hole,
The area S geometrically projected onto the bath surface is the bath surface area.
Indicates the proportion of Ls. Next, the relationship between hot metal temperature and exhaust gas CO/CO 2 +CO is as shown in Figure 3.
It is clear that the CO/CO 2 +CO ratio decreases rapidly below 1500°C, and that there is a critical point at 1500°C.
The figure shows flashing point area/bath surface area = 0.65, slag amount 10Kg/
According to experiments, the hot metal temperature can be maintained at 0.3 or higher while keeping the hot spot area/bath surface area at 0.3 or higher.
A decrease in the CO/CO 2 +CO ratio was confirmed when controlling the temperature below 1500°C. Furthermore, the relationship between the amount of slag in the furnace and CO/CO 2 +CO in the exhaust gas is as shown in Figure 4. 2 The relationship between +CO and slag amount is 15Kg/t.
It is clear that above this level, the value will rise rapidly. The spark spot area/bath surface area in the figure is 0.6. As a result of examining the above elemental conditions, in the carburization melting and refining method, the most efficient decarburization reaction using top-blown oxygen gas actively causes the reaction with the highest calorific value of C + O 2 → CO 2 , and the furnace The means of optimizing internal heat efficiency is the firing point area/bath area during oxygen gas decarburization refining>
0.5 and bath depth/bath inner diameter ≧0.5. Note that when the hot metal temperature is maintained below 1500℃, this value can be expanded to 0.3 respectively. Furthermore, according to the present invention, in addition to the hot spot area/bath surface area conditions, the hot metal temperature during oxygen gas decarburization refining is
It was confirmed that it is desirable to maintain the temperature at 1500°C or lower, and that it is most efficient when an elemental technology is added to control the amount of slag during oxygen gas decarburization refining to 15 kg/t or lower. Next, an application example of the carburization melting and refining method of the present invention will be explained. FIG. 5 shows the apparatus of the invention. In the figure, the carburization tank 10 has a slag hole 12, a bottom-blown stirring gas hole 14, a carburization agent injector 11, a scrap iron and iron ore input device 23, and a separation wall 13 at the boundary with the decarburization melting and refining tank 21. establish. The separation wall 13 separates the carburization tank 10 and the decarburization melting and refining tank 21 in the upper region of the hot metal, and forms a flow path for the molten metal in the bottom of the tank. The decarburization melting and refining tank 21 has an oxygen gas lance 22, a tapping hole 24, a bottom blowing stirring gas hole 25, and an electromagnetic stirring device 26 is provided near the conduction area of the separation wall. According to the present invention, after charging a small amount of hot metal into a melting and refining furnace consisting of two tanks (or leaving it in the furnace in advance), in the carburization tank, while blowing bottom-blown stirring gas, a carburizing agent is added to the top of the furnace. It is added to hot metal by charging at a more appropriate time or by injection method. When more than a certain amount of slag is generated, the slag is naturally drained from the slag drainage hole, or it is forcibly removed using a slag cleaner or the like. On the other hand, in the decarburization melting and refining tank, the hot metal bath depth (m)/
Continue decarburization refining while blowing top-blown oxygen and bottom-blowing gas to strengthen stirring so that the hot metal bath inner diameter (m) is maintained at 0.5 or more and the hot spot area/bath surface area≧0.50. Also, at least while carburization is being carried out in the carburization tank, oxidizing substances such as scrap or iron ore are added from above to prevent the hot metal temperature from exceeding 1500°C. If necessary, a refining agent such as lime or fluorite is added. According to experiments, the temperature of hot metal
When controlling below 1500℃, L/D and S/Ls
can be 0.3 or higher. After the necessary amount of carburization and melting, the hot metal can be poured out, or the decarburization and refining can be continued and the steel can be tapped when the required molten steel temperature and carbon content are reached. The separation wall between the decarburization melting and refining tank and the carburization tank is sufficient as long as the molten pig iron in the smelting tank and the carburization tank can mix with each other in the lower layer of the molten pig iron, and its main purpose is to separate the decarburization melting tank and the carburization tank. This prevents slag from the coal tank from flowing into the smelting tank. By doing the above, it became possible to digest a large amount of scrap with extremely high thermal efficiency, and it also became possible to reduce a large amount of oxides such as iron ore. FIG. 6 is an explanatory diagram of another example of application of the present invention. The carburization tank 10 and the decarburization melting and refining tank 21 are the same as those shown in FIG. A desulfurizing agent injection tank 32 is provided, and a bottom blowing stirring gas blowing hole 14-2 is provided. This example adds a desulfurization tank, but the desulfurization method is
It is possible to charge the desulfurizing agent upward and stir the gas from the bottom, or it is also possible to blow it in with an injection lance. As a method to prevent the slag from each reaction tank from entering the decarburization tank, in addition to separating the hot metal from each tank at the top in one container as described above, It is also possible to connect the containers by an electromagnetic force transfer method, a vacuum suction transfer method, etc., and transfer and mix the molten metal from each other. FIG. 7A shows a plan view of still another application example of the present invention. Decarburization melting and refining tank 21, carburization tank 10, desulfurization tank 3
This is a box-shaped three-tank separation type melting and refining furnace in which 1. 27 is a vacuum slag cleaner, and 19 is a hot metal transfer hole (FIG. 7B). That is, according to this example, in the first tank 21, oxygen gas is blown from the top using a lance 22, stirring gas is blown from the bottom, and iron ore charging device 21 is used to perform melting and refining. Crude molten steel is introduced into the second tank 10, coal powder is injected with the top blowing lance 11, and the generated slag is passed through the slag hole 1.
Discharge in 2. In the third tank 31, the desulfurization agent is returned to the first layer 21 after desulfurization using the injector 32, and continuous operation can be performed. FIG. 8 is a schematic diagram showing still another example of application of the present invention. In the figure, the carburization tank 10, the decarburization melting and refining tank 21, and the desulfurization tank 31 are connected to each other through a passage 36,
The molten metal is transferred by an electromagnetic transfer device 35. The slag off 12 is placed in the carburization tank 10, and the desulfurization (dephosphorization) tank 31
A slag-off 33 is provided in the molten steel, and molten steel is tapped from the decarburization melting and refining tank 21 into a ladle 27. Although the present invention has been described above with reference to an example in which the present invention is mainly applied to a separate continuous furnace, it does not depart from the scope of the present invention to operate with a single batch type furnace, unless it is contrary to the purpose of the present invention. As mentioned above, in carrying out carburization melting and refining of hot metal, the present invention provides a stirring gas bottom blowing hole in the bottom of the furnace, separates the upper layer region of the hot metal with a separation wall, and configures at least two tanks. By forming a coal tank and a decarburizing melting and refining tank, and adding a desulfurization tank as a third tank if necessary, a large amount of auxiliary raw materials such as iron ore and scrap iron can be processed in combination with coal addition during oxygen gas top-blowing refining. It makes charcoal melting and refining possible and has great industrial effects. Example 1 In a 180t oxygen top-blowing, Ar gas bottom-blowing combined refining furnace, the bath diameter was L3.2m, bath depth D3.2m (L/D=1.0, hereinafter referred to as L/D), and the oxygen was blown from the top-blowing lance. Spark spot area on the steel bath surface (total area of collision of oxygen gas against the steel bath surface ≒ N × (R + l・tanQ) 2 × π N = number of lance nozzles R = lance hole radius l = lance height Q = nozzle throat Adjust the lance height so that the angle is 5.6m 2 (flame area ratio 0.7), and as shown in Table 1, C +
By actively promoting the O 2 → CO 2 reaction, we were able to melt a large amount of scrap and refine steel.
【表】
実施例 2
200t酸素上吹、Arガス底吹の複合精錬炉にお
いて浴径3.2m、浴深3.2m(L/D=1.0)で、酸
素上吹ランスからの鋼浴表面上での火点面積が、
5.6m2になるようにランス高さを調整し、且つ鋼
浴中C%が1%以上での鋼浴内温度が1450℃以下
になるよう、酸素精錬中に炉内に鉄鉱石を添加し
精錬した結果、第2表に示す様に、C+O2→CO2
の反応を積極的に実施し、多量の鉄鉱石を使用
し、鉄歩留の高い精錬を実施する事が出来た。[Table] Example 2 In a composite refining furnace with 200t oxygen top blowing and Ar gas bottom blowing, the bath diameter was 3.2 m and the bath depth was 3.2 m (L/D = 1.0). The flash point area is
The lance height was adjusted to 5.6m2 , and iron ore was added to the furnace during oxygen refining so that the temperature in the steel bath was 1450℃ or less when the C% in the steel bath was 1% or more. As a result of refining, as shown in Table 2, C + O 2 → CO 2
By proactively carrying out this reaction, we were able to use a large amount of iron ore and carry out smelting with a high iron yield.
【表】
実施例 3
第5図に示す溶銑上部2槽分離型の梨型溶解精
錬炉において溶銑を50t装入後、浴径2.6m、浴深
1.3m(L/D=0.5)の加炭槽側で500Kg/分の速
度でコークス粉を上部より溶銑面上にN2ガスで
吹付けながら、脱炭精錬槽では、多孔ランスを使
用し、火点面積/浴表面積=65%で、通酸速度
500Nm3/分で吹錬し、炉底部から多孔、小径ノ
ズル(耐火物)で、600Nm3/時のArガスを両槽
に吹き込み、脱炭槽のスラグを10Kg/t−鋼以下
に維持した。
尚、加炭中溶銑温度が1400℃以上にならないよ
うに、脱炭溶解精錬槽に精錬中の溶銑温度に従つ
て、適時スクラツプを投入し、その後脱炭精錬
し、第3、第4表に示すように、極めて効率的に
多量スクラツプを溶解して、粗溶鋼を製造する事
が出来た。[Table] Example 3 After charging 50 tons of hot metal in the pear-shaped melting and refining furnace with two separated hot metal tanks shown in Figure 5, the bath diameter was 2.6 m and the bath depth was
While blowing coke powder with N2 gas from the top onto the hot metal surface at a speed of 500 kg/min in the 1.3 m (L/D = 0.5) carburization tank side, a porous lance was used in the decarburization refining tank. Fire point area/bath surface area = 65%, acid passing rate
Blowing was carried out at a rate of 500Nm 3 /min, and 600Nm 3 /hour of Ar gas was blown into both tanks from the bottom of the furnace through a porous, small diameter nozzle (refractory) to maintain the slag in the decarburization tank below 10Kg/t-steel. . In addition, in order to prevent the hot metal temperature during carburization from exceeding 1400℃, scrap is added to the decarburization melting and refining tank at appropriate times according to the hot metal temperature during refining, and then decarburization is performed. As shown, it was possible to melt a large amount of scrap extremely efficiently and produce crude molten steel.
【表】【table】
【表】
実施例 4
第7図に示す箱型3槽分離型溶解精錬炉におい
て、第1槽では浴径2.0m、浴深2.0m(L/D=
1.0)として上部より酸素ガスを3本ランスで、
火点面積/浴表面積=70%で、1400Nm3/分で吹
製し、底部3ケ所よりArガスを300Nm3/時各々
ノズルにて底吹し、上部より鉄鉱石を投入した。
尚第1槽の先端部では、鉄鉱石から発生するスラ
グを真空スラグクリーナで適時排出した。
続く第2槽では、石炭粉を上吹ランスにより浴
銑中にインジエクシヨンし、先端部より石炭より
発生するスラグを連続排滓した。
最後の第3槽では、生石灰と螢石を上吹ランス
で溶銑中にインジエクシヨンし、先端部よりスラ
グクリーナで適時排滓を実施した。この第3槽の
溶銑を再度第1槽に戻し、連続的にこの処理をく
り返す事によつて、第5表に示す様な溶銑を効率
的に鉄鉱石から製造する事が出来た。[Table] Example 4 In the box-type three-tank separated melting and refining furnace shown in Fig. 7, the first tank has a bath diameter of 2.0 m and a bath depth of 2.0 m (L/D =
1.0), oxygen gas is supplied from the top with three lances,
Blowing was carried out at 1400 Nm 3 /min at a firing point area/bath surface area = 70%, Ar gas was blown at 300 Nm 3 /hour from three nozzles at the bottom, and iron ore was introduced from the top.
In addition, at the tip of the first tank, slag generated from iron ore was timely discharged using a vacuum slag cleaner. In the subsequent second tank, the coal powder was injected into the bath iron using a top blowing lance, and the slag generated from the coal was continuously removed from the tip. In the third and final tank, quicklime and fluorite were injected into the hot metal using a top blowing lance, and the slag was removed from the tip using a slag cleaner. By returning the hot metal in the third tank to the first tank and repeating this process continuously, hot metal as shown in Table 5 could be efficiently produced from iron ore.
【表】
実施例 5
浴径2.0m、浴深2.0m(L/D=1.0)とした脱
炭溶解精錬槽、加炭槽、脱硫脱燐槽を第8図の如
く、ほぼ同一水準レベルに設置し、各々の槽を耐
火物導管にて連絡し、その導管の外側に、脱炭槽
→加炭槽、加炭槽→脱硫脱燐槽、脱硫脱燐槽→脱
炭槽に溶銑が移送循環される様に、電磁誘導コイ
ルを設置した。
まず、初期に各槽の連結導管が溶銑面になるよ
う30tの溶銑を槽内に装入した後、初期レベルL1
の各槽で第6表のような反応を実施させた。[Table] Example 5 A decarburization melting and refining tank, a carburization tank, and a desulfurization and dephosphorization tank with a bath diameter of 2.0 m and a bath depth of 2.0 m (L/D = 1.0) were made to almost the same level as shown in Figure 8. The hot metal is transferred to the decarburization tank → carburization tank, carburization tank → desulfurization and dephosphorization tank, and desulfurization and dephosphorization tank → decarburization tank. An electromagnetic induction coil was installed to ensure circulation. First, 30 tons of hot metal is initially charged into the tank so that the connecting pipes of each tank are on the hot metal surface, and then the initial level L 1
The reactions shown in Table 6 were carried out in each tank.
【表】
尚各槽間を毎分20tの速度で溶銑を移動しなが
ら実施し、1時間後に130t(最終レベルL2)の溶
鋼(C=0.10%、P=0.25%、S=0.010%)を製
造する事が出来たので、脱炭槽より取鍋に100t排
出し、ひきつづき連続的に屑鉄溶解をつづける事
が出来た。
実施例 6
第9図に図示する浴径2.3m、浴深1.6m(L/D
=0.7)の精錬炉101に50tの予備処理溶銑を受
け、上部より酸素ガス102を鋼浴火点面積率で
0.70になるように吹きつけ、且つ上部103より
スクラツプ25t、コークス2tを連続的に投入し、
精錬中の鋼浴温度を1400℃以上にならないよう調
整した。
この時同時に炉底部よりAiガス104を0.12N
m3/t−分羽口より吹き込み、鋼浴の撹拌を強化
した。
その後精錬炉に発生したスラグを排出するため
精錬を中断し、図示の様に真空排滓機105で炉
内のスラツグを完全排除し、その後前述したと同
様な方法で、上部103−2からスクラツプ25t、
コークス6tの添加を実施しながら加炭溶解精錬を
実施し、100tの溶銑を製造する事が出来た。第7
表に操業条件を示した。[Table] The process was carried out while moving the hot metal between each tank at a speed of 20 tons per minute, and after one hour, 130 tons (final level L 2 ) of molten steel (C = 0.10%, P = 0.25%, S = 0.010%) Since we were able to produce 100 tons of scrap iron from the decarburization tank into a ladle, we were able to continue melting scrap iron continuously. Example 6 The bath diameter is 2.3 m and the bath depth is 1.6 m (L/D
= 0.7), 50 tons of pre-treated hot metal is received in the refining furnace 101, and oxygen gas 102 is injected from the top at the steel bath hot spot area ratio.
0.70, and 25 tons of scrap and 2 tons of coke were continuously introduced from the upper part 103.
Adjusted the temperature of the steel bath during refining so that it does not exceed 1400℃. At the same time, 0.12N of Ai gas 104 was added from the bottom of the furnace.
The stirring of the steel bath was intensified by blowing through the tuyere at a rate of m 3 /t-min. After that, the refining is interrupted to discharge the slag generated in the refining furnace, and as shown in the figure, the slag in the furnace is completely removed by the vacuum slag machine 105, and then the scrap is removed from the upper part 103-2 in the same manner as described above. 25t,
Carburizing, melting and refining was carried out while adding 6 tons of coke, and we were able to produce 100 tons of hot metal. 7th
The operating conditions are shown in the table.
【表】【table】
第1図は火点面積/浴表面積の模式図、第2
図、第3図、第4図はL/D比別の排ガス中の
CO/CO2+COの図表、第5図は本発明の実施例
の部分断面図、第6図は本発明の他の実施例の部
分断面図、第7図イは本発明の更に他の実施例の
部分断面平面図、ロは部分断面正面図、第8図は
本発明の更に他の実施例の説明図、第9図は本発
明の更に他の実施例の説明図である。
10;加炭槽、12;排滓孔、13;分離壁、
14,25;撹拌ガス底吹孔、24;出鋼孔。
Figure 1 is a schematic diagram of the flash point area/bath surface area, Figure 2
Figures 3 and 4 show the differences in exhaust gas by L/D ratio.
A diagram of CO/CO 2 +CO, FIG. 5 is a partial sectional view of an embodiment of the present invention, FIG. 6 is a partial sectional view of another embodiment of the present invention, and FIG. FIG. 8 is an explanatory diagram of still another embodiment of the present invention, and FIG. 9 is an explanatory diagram of still another embodiment of the present invention. 10; carburization tank, 12; slag drainage hole, 13; separation wall,
14, 25; Stirring gas bottom blowing hole, 24; Steel tapping hole.
Claims (1)
材を添加する酸素上吹精錬法において酸素ガス吹
精時にL/D≧0.5、S/LS≧0.5に保持すること
を特徴とする溶銑の加炭溶解精錬方法。 ただしL;溶銑浴深さ(m)D;溶銑浴内径
(m) S;火点面積 LS;溶銑浴表面積 2 ガス状物質の底吹きを伴い、かつ溶銑に炭素
材を添加する酸素上吹精錬法において、酸素ガス
吹精時にL/D≧0.3、S/LS≧0.3に保持すると
ともに、酸素ガスによる脱炭精錬時の溶湯を1500
℃以下に制御することを特徴とする溶銑の加炭溶
解精錬法。 ただしL;溶銑浴深さ(m)D;溶銑浴内径
(m) S;火点面積 LS;溶銑浴表面積 3 酸素ガスによる脱炭精錬中のスラグ量を溶鋼
t当り15Kg以下に制御することを特徴とする特許
請求の範囲第2項記載の溶銑の加炭溶解精錬方
法。[Claims] 1. Maintaining L/D≧0.5 and S/LS≧0.5 during oxygen gas blowing in an oxygen top-blowing refining method that involves bottom blowing of gaseous substances and adding carbon material to hot metal. A method for carburizing, melting, and refining hot metal. However, L: Hot metal bath depth (m) D: Hot metal bath inner diameter (m) S: Hot spot area LS: Hot metal bath surface area 2 Oxygen top-blowing refining that involves bottom blowing of gaseous substances and adding carbon material to hot metal. In the method, L/D≧0.3 and S/LS≧0.3 are maintained during oxygen gas blowing, and the molten metal is kept at 1500 ml during decarburization refining using oxygen gas.
A hot metal carburization melting and refining method characterized by controlling the temperature to below ℃. However, L: Hot metal bath depth (m) D: Hot metal bath inner diameter (m) S: Hot spot area LS: Hot metal bath surface area 3 The amount of slag during decarburization refining with oxygen gas should be controlled to 15 kg or less per ton of molten steel. A method for carburizing, melting and refining hot metal according to claim 2.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58132821A JPS6026606A (en) | 1983-07-22 | 1983-07-22 | Method for subjecting molten iron to recarburization melt-refining |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58132821A JPS6026606A (en) | 1983-07-22 | 1983-07-22 | Method for subjecting molten iron to recarburization melt-refining |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6026606A JPS6026606A (en) | 1985-02-09 |
| JPS6315325B2 true JPS6315325B2 (en) | 1988-04-04 |
Family
ID=15090346
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP58132821A Granted JPS6026606A (en) | 1983-07-22 | 1983-07-22 | Method for subjecting molten iron to recarburization melt-refining |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6026606A (en) |
-
1983
- 1983-07-22 JP JP58132821A patent/JPS6026606A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6026606A (en) | 1985-02-09 |
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