JPS635450B2 - - Google Patents

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Publication number
JPS635450B2
JPS635450B2 JP9656980A JP9656980A JPS635450B2 JP S635450 B2 JPS635450 B2 JP S635450B2 JP 9656980 A JP9656980 A JP 9656980A JP 9656980 A JP9656980 A JP 9656980A JP S635450 B2 JPS635450 B2 JP S635450B2
Authority
JP
Japan
Prior art keywords
oxygen
furnace
molten steel
hot metal
slag
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
JP9656980A
Other languages
Japanese (ja)
Other versions
JPS5723016A (en
Inventor
Toshio Kishida
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 JP9656980A priority Critical patent/JPS5723016A/en
Publication of JPS5723016A publication Critical patent/JPS5723016A/en
Publication of JPS635450B2 publication Critical patent/JPS635450B2/ja
Granted legal-status Critical Current

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Classifications

    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P10/00Technologies related to metal processing
    • Y02P10/20Recycling

Landscapes

  • Refinement Of Pig-Iron, Manufacture Of Cast Iron, And Steel Manufacture Other Than In Revolving Furnaces (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明はアーク炉製鋼法の改良に係り、特に著
しい生産性の向上と省エネルギー効果に加えて、
高い精錬歩留り、低減された廃棄物量、更には炉
壁損耗の抑制などを効果的に達成した製鋼法を提
供するものである。 製鋼の主体が平炉から転炉へ移つて行つた過程
で、アーク炉製鋼は依然としてその地位を保つて
きた。これを支える最大のものは、アーク炉製鋼
の生産能率の著しい向上である。 溶銑などを原料に操業する転炉製鋼とくらべた
とき、アーク炉製鋼はスクラツプなどの冷材から
操業を開始するという不利を負つているので、ア
ーク炉製鋼の生産能率の向上は、装入物の溶解に
要する時期とエネルギーをいかに節減するかにか
かつている。このためにとられた主要な対策は、
一つは単位時間あたりの投入電力量を増大する、
いわゆるUHP電気炉操業であり、いま一つは電
力以外にエネルギー源を求めた、助燃バーナーの
利用である。これらは一応の成果をおさめたとい
えるが、トランス容量やバーナー能力などの使用
設備からの限界は、当然にある。 そこで、この限界を打破するために試みられた
のが、酸素ガスの活用である。すなわち、装入物
の溶解中および溶解末期に設備の許容する範囲内
で最大量の酸素ガスを炉内に吹き込み、平滑鋼浴
面形成後は脱炭のために要する以上の量の酸素
を、送電(アーク加熱)を続けながら、溶鋼中に
吹き込む操業である。また、助燃バーナーを有す
る設備では、オイルの燃焼に必要な量を超える酸
素を、バーナーを通して送気する。こうした操業
を、本発明者は、アーク炉製鋼における酸素富化
操業とよんでいる。この酸素富化操業は、炭素、
ケイ素、鉄分などのアーク炉装入物中の諸成分が
投入酸素により酸化される際の反応熱により、固
型物の溶解促進と溶鋼の昇温促進が行なわれ、ま
た炉壁に付着した未溶解固形物が酸素により強制
的に溶断され炉内不均一溶解が解消するといつた
効果があるので、生産能率が大いに向上する。 そして、かくの如き酸素富化操業の利益は時間
の短縮だけでなく、アーク炉で溶解および精錬に
必要とする電力量の大幅な低減をも可能にする。
アークによる入熱は、炉の構造上、装入物または
鋼浴の上方から行なわれるので、アークの上方へ
の反射などでエネルギーが失なわれることは、あ
る程度までは避けられない。一方、酸素との反応
による熱は装入物の表面または鋼浴中で発生する
ので、そのエネルギーは大部分が利用される。従
つて、酸素ガスの使用量をエネルギーに換算して
電力のエネルギーと合計し、全投入エネルギーの
原単位を考えるとき、その値は酸素ガス投入量の
増大に伴つて向上する(酸素投入量10Nm3/装入
トンで10%以上、20Nm3/装入トンで20%に達す
る)。 このように、酸素富化操業は有利なアーク炉製
鋼法ではあるが、その利益を追及して行く過程で
新たな困難に遭遇した。その一つは、スクラツプ
等の装入原材料重量に対して得られる溶鋼重量の
割合、すなわち溶解歩留りの低下であり、いま一
つは、これと表裏の関係にあるが、溶解残渣であ
るスラグ量の増加である。また、上述のように酸
素富化操業が電力量の大幅な低減を可能にすると
いつても、酸素投入による反応熱の発生は炉内に
溶融物が形成された後において有効となるもので
あり、装入原材料の溶解は基本的にはアーク加熱
によるものであるため、酸素投入による電力エネ
ルギーの低減にも自ら限度があるのである。 ここにおいて、本発明は、かかる事情を背景に
して為されたものであつて、その目的とするとこ
ろは、酸素富化操業の有利さを活用しつつ、生産
性の著しい向上と省エネルギー、特に電力エネル
ギーの大巾な節約を図り得るアーク炉製鋼法を提
供することにある。また、本発明の他の目的は、
上記酸素富化操業における困難を取り除き、生産
能率の向上と省エネルギー化を達成しつつ、溶解
歩留りの向上、廃棄物となるスラグ量の増加の抑
制、更には炉壁の損耗の抑制などの効果を奏し得
る製鋼法を提供することにある。 そして、これらの目的を達成するため、本発明
は下記の工程をふむことを特徴としている。すな
わち、アーク炉製鋼において、 (a) 溶解期または酸化期、あるいはその両方にわ
たつて、炉内に酸素を吹き込んで、炭素含量が
0.20%以下、好ましくは0.15%以下の溶鋼を得
ること、及びそれに続いて、 (b) アーク加熱並びに酸素の吹込みを行ないつ
つ、少なくとも約2%の炭素を含有する溶銑を
連続的に炉内に装入すること。 かくの如き本発明に係る操作の第一の段階(a)は
既知の手法に従えばよく、例えば所定のアーク炉
内にスクラツプ(鉄くず)などの原材料を装入し
て通常の条件下にアーク加熱せしめればよい。ま
た酸素ガスは通常のランスパイプ(第1図におい
て、6)を用いて吹き込んでもよいし、更に助燃
バーナーを用いる場合にはオイルの燃焼に必要な
量を超える酸素を送り込んでもよい。なお、吹き
込まれる酸素ガスとしては、よく知られているよ
うに、純酸素ガス或は酸素富化空気が好適に用い
られるものである。 また、第二の段階(b)の状況を模式的に示せば、
第1図のとおりであつて、アーク炉1内では電極
(通常は3本の電極が用いられているが、ここで
は説明を簡略にするためにそのうちの一本のみが
図示されている)2と溶鋼3との間でアークを発
生させて加熱精錬を行なつており、溶鋼3表面は
スラグ4が覆つている。また、ランスパイプ6が
出滓口(操業口)に設けられた小孔5を通つて炉
内の溶融物中に挿入されており、該ランスパイプ
6を通じて酸素が吹き込まれている。なお、ラン
スパイプ6の先端6Aの位置は、通常は溶鋼3と
溶融スラグ4との境界付近が適当であるが、鋼中
に存在させるべき炭素の量や精錬の段階に応じ
て、適宜上下させられ、溶鋼3中に、あるいはス
ラグ4中に移されたりする。さらに、約2%以上
の炭素含量の高い溶銑を収容する耐火物製の容器
7が、アーク炉1側方に設けられており、該容器
7から炉壁の出滓口(操業口)を貫通して炉内に
開口する耐火物製の樋8を通じて、かかるアーク
炉1内に溶銑が所定の割合で連続的に装入せしめ
られる。そして、このようにアーク加熱及び酸素
の吹込みを続けながら、溶銑を連続的に装入する
と、後述するように、溶融スラグ4が盛り上がる
ようになるのである。 上記構成を採択した意義のよりよい理解のため
には、本発明の成立に至る経緯を説明することが
適切と思われるので、以下に述べる。 周知のとおり、溶鋼上に存在する溶融スラグ中
の酸化鉄含有率は、溶鋼中の酸素含有率(正確に
いえば活動度であるが)に支配され、溶解中の酸
素含有率が高いほどスラグ中の酸化鉄含有率も高
くなる。一方、溶鋼中の酸素含有率は、酸素富化
操業のように酸素の供給が十分な条件下では、主
として溶鋼中の炭素含有率によつて決定される。 溶鋼中の炭素含有率と酸素含有率との関係は古
くから研究され、いわゆる「バツチヤー・ハミル
トンの関係」としてよく知られるグラフが各種ハ
ンドブツクに掲載されている。それによれば、一
般に溶鋼中の炭素含有率が高くなるほど、酸素含
有率は低くなる。従つて、その溶鋼と共存するス
ラグ中の酸化鉄含有率もまた低くなるはずであ
る。逆に、溶鋼中の炭素含有率が低いことは酸素
含有率が高いことを意味し、スラグ中の酸化鉄含
有率が高くなる結果を招く。 本発明者が酸素富化操業の探究の過程で溶解歩
留りの改善を企てたとき、最初に試みた対策は、
上記の理解にもとづいて溶鋼組成を調節すること
であつた。すなわち、スクラツプなどの原材料と
ともにアーク炉に装入しておく炭素付加材(先入
れ加炭材)の量を増したり、種類をえらぶことに
より、酸素富化操業終了の時点における溶鋼中の
炭素含有率を適切な水準に維持し、それによつて
溶鋼中の酸素含有率を相対的に低位に保つことで
ある。 この先入れ加炭材による溶鋼中炭素含有率の調
節は、炉内に送り込む酸素の量が5〜6Nm3/装
入トン程度までは、おおむね効果的であつて、酸
素富化操業の利益をある程度享受しつつ、溶解歩
留りの低下やスラグ量の増大を若干はおさえるこ
とができた。 しかし、酸素富化操業の利益を十分に得るため
には、酸素投入量をより大きくしなければならな
い。ところが、10Nm3/装入トンまたはこれを上
回る大量の酸素を使用する場合には、もはや先入
れ加炭材により溶鋼中の炭素含有率を維持するの
は不可能なことが経験された。それは、通常の装
入手段で与えられる炭素は、ほとんど酸素により
燃焼してしまい、溶鋼中に溶解する分がなくなつ
てしまうからである。先入れ加炭材を極度に増し
てみても、精錬過程で一部排出するスラグに混つ
て炉外に出てしまつたり、炉壁に固着する末溶解
物中に保持され、その後の精錬過程で溶鋼中に落
下して精錬作業を妨げたりするおそれがある。 このような経験にかんがみ案出されたのが本発
明による高炭素含量である溶銑を装入する方式で
ある。 この本発明方式における新規な点は、溶鋼中の
炭素含有率を一旦は低い水準まで下げてから再び
炭素を与えることにある。すなわち、酸素富化操
業の実施に際して、前記バツチヤー・ハミルトン
の関係に立脚して溶鋼中の炭素含有率を維持しな
がら操業するという、当業技術において従来は常
識とされていた考えを捨て、溶鋼中の炭素含有率
の低下、ひいては鉄分の酸化を気にかけずに十分
な量の酸素ガスを炉内に投入し、のちにこの酸素
により燃焼して生成した酸化鉄を炭素により還元
して金属鉄として回収するという改善案を提示し
たことが本発明の意義である。 なお、アーク炉内で起る諸化学反応にも、当然
にヘスの法則が適用されるので、酸素富化操業に
伴つて得られた鉄の酸化による発熱が、酸化鉄の
還元過程で相殺されてしまうのではないか、とい
う懸念があろう。同一量の酸素が鉄と反応した場
合と炭素と反応した場合とでは、 Fe+O=FeO+109.6Kcal/mol・O2 C+O=CO+52.8Kcal/mol・O2 前者の方が発熱は大きいが、 FeO+C→Fe+CO−56.8Kcal/mol・O2 の吸熱により、結局は炭素の燃焼熱しか利用でき
ないように思われた。 ところが、後に示す実施例から明らかなよう
に、アーク加熱並びに酸素吹込み下における高炭
素含量の溶銑の装入により、酸素富化操業のもた
らす省エネルギー効果が減じることはない。この
最大の理由は、前記したスラグの発泡によるもの
と解される。すなわち、溶銑を介しての炭素の導
入により酸化鉄が還元され一酸化炭素が生成し、
これが吹き込まれる酸素とともにスラグを泡立て
る結果、その泡沫層の上部は吹き込み前からみる
と50cm〜1mも盛り上がつて送電中の電極の先端
を包み込み、アークが完全にスラグ中に埋没して
その発熱が高度に利用されるという現象である。 そして、このようなフオーミング現象に基づく
スラグ上部の泡沫層の形成により、このスラグ泡
沫がアークを包み込むと共の溶鋼の保温にも役立
ち、電力原単位の向上と所要時間の短縮が達成さ
れるのである。しかも、スラグの中でアークが飛
んでいるような状態となるため、アークによる直
接的な影響やアーク音、スラグ表面からの輻射熱
に基づく炉壁の溶損の抑制も効果的に達成され得
るのである。特に、本発明にあつては、その前段
の酸素富化操業により溶鋼およびスラグ中の酸素
含有率が高まつているところへ炭素を導入した形
となるので、一酸化炭素ガスの発生量が多く、上
記した効果はより一層顕著になる。本発明者の経
験によれば、酸素富化操業後に溶銑の装入(炭素
の導入)をしない場合の電力による昇温時の熱効
率は約30%であるのに対し、溶銑の装入を行なつ
た場合にはこれが約60%に向上する。この効率の
向上は、たとえば公称能力70トン炉において300
Kgの炭素を含む溶銑を5分間で導入した操業例に
おいて酸化鉄の還元による吸熱を補うのに十分な
ものである。 次に本発明の構成について説明を補足する。 酸素の吹き込みにより溶鋼中の炭素含有率を、
0.20%以下、好ましくは0.15%以下、通常の操業
においては0.10%以下にすることは、アーク炉に
よる精錬プロセス自体にとつて不可欠というより
は、酸素富化操業の結果として到達する条件であ
る。換言すれば、酸素富化操業の利益を確保する
に十分な量の酸素の吹き込みが行なわれたこと
が、上記の溶鋼中炭素含有率によつて確認される
わけである。操業のめやすを与えるという点で、
この条件は重要な意義をもつている。実操業の面
からいえば、上記の溶鋼中炭素含有率を与える酸
素吹込量は、通常10Nm3/装入トンまたはそれ以
上である。 こうした条件は、本発明者が酸素富化操業の探
究過程で経験的に見出したものであるが、70トン
アーク炉における脱炭試験の結果からも支持され
る。第2図は、酸素吹き込みによる脱炭を行なう
際の、溶鋼中の炭素含有率と脱炭速度との関係を
示すグラフである。このグラフから明らかなよう
に、溶鋼中の炭素含有率が0.20%以下、より明確
には0.15%以下になると、脱炭反応は酸素供給律
速から炭素拡散律速に変り、この限界値以下の炭
素含有率においては、炉内に供給された酸素は主
として鉄分を酸化してゆくことになる。しかしな
がら、本発明に従うときは酸化により鉄分が失わ
れても、後の炭素吹き込みによつて回復するか
ら、溶鋼の炭素含有率を、たとえば0.10%以下の
ような低い値にしても、何ら不利益ない。従つ
て、炭素含有率の低下を気にすることなく、酸素
富化操業の利益が十分に得られる程度まで、酸素
の吹き込みを行なうことができる。 また、本発明に従つて炉内に連続的に装入せし
められる溶銑としては、少なくとも約2.0%の炭
素を含有するものを用いる必要があり、炭素含有
が余りに低いものは酸化鉄の還元に効果的に寄与
せず、本発明の目的を充分に達成することが困難
である。特に、本発明にあつては、溶鉱炉(高
炉)若しくはキユポラで製造される3〜4%程
度、あるいはそれを越える高炭素含量の溶銑が有
利に使用されることとなる。溶鉱炉またはキユポ
ラでは石炭エネルギーにて溶銑が製造されるもの
であるため、そのような溶銑を用いることによ
り、アーク炉製鋼における全体としての消費電力
量が著しく低減され得るのである。けだし、該溶
銑中の炭素成分を酸化鉄の還元に利用する一方、
該溶銑の主成分たる鉄成分はそのままアーク炉製
品たる溶鋼成分と為し得るからであり、そこに本
発明の著しい特徴が存するのである。換言すれ
ば、本発明の狙いとするところは、除去されるべ
き溶銑中の炭素をアーク炉製鋼における酸化鉄の
還元に用いることによつて同時に溶銑も溶鋼に変
換されるという一石二鳥的作用を利用することに
より、アーク炉における電力エネルギーの削減は
もとより、溶鋼生産性の大巾な向上を達成せしめ
るところにあるのである。なお、このような溶銑
は、最終的に全装入物の10〜50%の割合となるよ
うに(従つて全装入物の50〜90%をスクラツプ等
の冷固型物が占めることとなる)、アーク炉内に
装入されることとなる。また、かかる溶銑の装入
は、該溶銑から供給される炭素量がアーク炉内に
存在する溶融物1トン当り0.2〜2.0Kg/分となる
ような割合において、行なわれることが望まし
い。この装入速度が余りにも遅い場合には効率が
悪くなるのであり、また余りにも速い場合には繰
返し溶解を進めたときなどに溶鋼品質の変動等の
問題が惹起され易い。 さらに、かくの如き溶銑の連続的な装入に際し
て、電極2によるアーク加熱は続行されており、
またランスパイプ6を通じての酸素ガスの吹き込
みも続けられている。従つて、この工程(b)で吹き
込まれる酸素ガスとしては、工程(a)と同様な純酸
素ガスや酸素富化空気が用いられることとなる。
このようなアーク加熱、酸素ガス吹き込み下にお
ける溶銑の連続的装入によつて、前記した如き酸
化鉄の効果的な還元、そしてそれによつて発生す
る一酸化炭素による有効な泡沫層の形成などが行
なわれ、以て本発明の優れた効果が達成され得る
のである。 なお、以上説明した具体例の他、本発明の趣旨
を逸脱しない限りにおいて、本発明には当業者の
知識に基づいて種々なる変更、修正等を加え得る
ものである。 以下に、公称能力70トンのUHPアーク炉を用
いた製鋼に例をとり、本発明を従来技術と比較し
つつ更に詳細に説明する。 比較例1 (従来方法) 市中購入スクラツプ32トン、社内発生返り屑21
トンを、コークス粉1トン、生石灰2トンととも
にアーク炉内に装入し送電(アーク加熱)を開始
した。33分後に送電を中断し、さらに34トンの市
中購入スクラツプを炉内に装入し、送電を再開し
た。最初の送電開始後64分の時点で、成分分析用
試料として溶鋼の一部をくみ取つた。この時点に
おける溶鋼中の炭素含有率は0.25%であつた。 その後、溶鋼中炭素含有率の低減(脱炭)を目
的に120Nm3の気体酸素をランスにより溶鋼中に
吹き込んだ、吹き込み完了後、再度分析試料を採
取した。この時点における溶鋼中の炭素含有率は
0.08%であつた。 酸素吹き込み完了後、送電(アーク加熱)によ
り鋼浴温度が1650℃に達した事を確認後、再度分
析試料を採取し、しかる後炉内にあるスラグを炉
外に排出した。この時点の溶鋼中炭素含有率は
0.06%であつた。同時に採取した炉内スラグの分
析値によれば、この時炉内にあつた溶滓中の酸化
鉄含有率は25%であつた。スラグ排出後、生石
灰、ホタル石と共に2.6トンの元素添加合金を炉
内に添加した。送電によりこれらの添加物が溶解
された後、鋼浴温度が1630℃になつた事を確認
し、炉内の溶鋼を炉外の取鍋に出鋼した。 出鋼後の溶鋼中炭素含有率は0.21%であつた。
出鋼後の溶鋼重量は86200Kgであり、従つて溶解
歩留は96.2%であつた。 脱炭、昇熱完了後に炉外に排出したスラグの重
量は5.1トンであつた。 全過程を通して使用された電力量を出鋼重量で
除した出鋼トン当りの電力原単位は510KWHで
あつた。 出鋼完了後のアーク炉内を耐火物にて補修し、
次の溶解のための材料を装入後、送電を開始した
のは、前溶解のための送電開始から121分後であ
つた。 比較例2 (酸素富化操業) 比較例1と同じ原料をアーク炉に装入して、送
電を開始した。送電開始10分後から、炉内にラン
スにより気体酸素を送気した。送電開始28分後に
送電と送気を中止し、34トンの市中購入スクラツ
プを炉中に装入し、送電を再開した。送電再開5
分後に炉内への気体酸素送気を再開した。そのま
ま操業を継続し、固型装入物のほとんどが鋼浴中
に入り平滑な湯面が形成された時、分析試料を採
取した。この時点での溶鋼中炭素含有率は0.10%
であつた。その後さらに鋼浴への送気を続け、併
せて送電しつつ鋼浴温度の上昇をはかつた。 鋼浴温度が1650℃に達したことを確認後、再度
分析試料を採取し、しかる後炉内にある溶融スラ
グを炉外に排出した。この時点での溶鋼中炭素含
有率は0.04%であつた。同時に採取した炉内スラ
グの分析値によれば、この時炉内にあつたスラグ
中の酸化鉄含有率は45%であつた。 スラグ排出後は比較例1と同様に操作して、取
鍋に出鋼した。 この操業により得られた鋼の溶解歩留は94.5%
であつた。炉外に排出されたスラグ量は7.2トン
であつた。 電力原単位は455KWH/溶鋼トン、気体酸素
使用量は1490Nm3であつた。送電開始から、次回
送電開始迄の1サイクル時間は87分であつた。 実施例 市中購入スクラツプ30トン、社内発生戻り屑20
トンを、コークス粉0.5トン、生石灰2トンと共
に、アーク炉内へ装入し、送電によりアーク加熱
を開始した。 送電開始の約10分後から、アーク炉内へランス
を通じて気体酸素を溶鋼中に吹き込み、そして炉
内のスクラツプが完全溶解し、溶鋼の温度が約
1500℃に達した後、成分分析用試料として炉内か
ら溶鋼及びスラグの一部を採取した。この時点で
の溶鋼中の炭素含有率は0.03%、スラグ中の酸化
鉄含有量は53%であつた。 引き続き、送電並びに気体酸素の吹込みを行な
いつつ、予めキユポラで溶解、製造された、含有
炭素量2.95%の1350℃の溶融銑鉄40トンを毎分2
トンの速度をもつてアーク炉内へ連続的に装入し
た。20分間を要して、かかる溶銑の全装入を完了
せしめ、そしてそれと同時に気体酸素の送気(吹
込み)を中止した。溶銑装入開始から終了までに
要した気体酸素は1100Nm3であつた。また、かか
る溶銑装入開始後しばらくして送電によるアーク
音が著しく小さくなり、炉中の溶融スラグは泡立
ち、約1m程盛り上がつていることが認められ
た。 ついで、かかる酸素気送中止から、送電下に溶
鋼を1680℃まで昇熱し、分析試料を採取した後、
炉内のスラグを炉外へ排出した。スラグ排出直前
の溶鋼中の炭素含量は0.1%、スラグ中の酸化鉄
含量は22%であつた。 スラグ排出後、生石灰、ホタル石と共に、2.5
トンの元素添加合金を炉内に添加し、送電により
これらの添加物が溶解せしめられた後、溶鋼温度
が1630℃になつたことを確認し、炉外の取鍋内に
溶鋼を出鋼した。 かかる出鋼された溶鋼量は89700Kgとなつた。
従つて、溶解歩留りは97%(=89700Kg/92500
Kg)となる。なお、炉外へ排出されたスラグは
2.4トンであつた。 送電開始より次回溶解の送電開始までの所要時
間は75分であつた。また、要した電力原単位は
265KWH/溶鋼トンであつた。 以上の結果をとりまとめると、次のとおりであ
る。この比較から、本発明によるアーク炉製鋼法
が、生産能率およびエネルギーコストの点で酸素
富化操業のレベルを更に著しく向上させた上で、
溶解歩留りが高く、スラグ排出量が少ないという
利益をもたらしていることが明らかである。
The present invention relates to an improvement of the arc furnace steel manufacturing method, and in addition to particularly remarkable productivity improvement and energy saving effects,
The present invention provides a steel manufacturing method that effectively achieves high refining yield, reduced amount of waste, and further suppresses furnace wall wear. While the mainstay of steelmaking shifted from open-hearth furnaces to converter furnaces, arc furnace steelmaking continued to maintain its position. The biggest support for this is the significant improvement in production efficiency of arc furnace steelmaking. Compared to converter steelmaking, which operates using raw materials such as hot metal, arc furnace steelmaking has the disadvantage of starting operations from cold material such as scrap. It depends on how the time and energy required for melting can be saved. The main measures taken for this purpose were:
One is to increase the amount of power input per unit time.
This is so-called UHP electric furnace operation, and another method is the use of an auxiliary burner, which seeks an energy source other than electricity. Although these efforts can be said to have achieved some success, there are naturally limitations due to the equipment used, such as transformer capacity and burner capacity. Therefore, attempts were made to utilize oxygen gas to overcome this limit. That is, during the melting of the charge and at the end of melting, the maximum amount of oxygen gas is blown into the furnace within the range that the equipment allows, and after the smooth steel bath surface has been formed, the amount of oxygen that is greater than that required for decarburization is blown into the furnace. This operation involves injecting into molten steel while continuing to transmit electricity (arc heating). In addition, in equipment having an auxiliary combustion burner, oxygen in excess of the amount required for combustion of oil is sent through the burner. The present inventor calls such an operation an oxygen-enriched operation in arc furnace steelmaking. This oxygen-enriched operation
The reaction heat generated when silicon, iron, and other components in the charge of the arc furnace are oxidized by the input oxygen accelerates the dissolution of solid matter and the temperature rise of molten steel, and also removes unfinished material that adheres to the furnace wall. Since the molten solids are forcibly melted by oxygen and uneven melting in the furnace is eliminated, production efficiency is greatly improved. The benefits of such oxygen-enriched operations are not only time savings, but also significant reductions in the amount of power required for melting and refining in arc furnaces.
Because the heat input by the arc is performed from above the charge or the steel bath due to the structure of the furnace, it is unavoidable to some extent that energy is lost due to upward reflection of the arc. On the other hand, since the heat due to the reaction with oxygen is generated on the surface of the charge or in the steel bath, most of the energy is utilized. Therefore, when converting the amount of oxygen gas used into energy and adding it up to the energy of electricity and considering the basic unit of total input energy, the value increases as the amount of oxygen gas input increases (oxygen input amount of 10Nm 3 /charging ton more than 10%, 20Nm 3 /charging ton reaching 20%). As described above, although oxygen-enriched operation is an advantageous arc furnace steelmaking method, new difficulties were encountered in the process of pursuing its benefits. One of these is a decrease in the melting yield, which is the ratio of the weight of molten steel obtained to the weight of charged raw materials such as scrap, and the other, which is related to this, is the decrease in the amount of slag, which is the melting residue. This is an increase in In addition, even though oxygen-enriched operation enables a significant reduction in power consumption as mentioned above, the generation of reaction heat due to oxygen injection becomes effective after the melt is formed in the furnace. Since the charging raw materials are basically melted by arc heating, there is a limit to the reduction in electric power energy by adding oxygen. The present invention has been made against this background, and its purpose is to significantly improve productivity and save energy, especially power consumption, while utilizing the advantages of oxygen-enriched operation. The object of the present invention is to provide an electric arc furnace steelmaking method that can save a large amount of energy. In addition, another object of the present invention is to
By eliminating the above-mentioned difficulties in oxygen-enriched operation, we have achieved improvements in production efficiency and energy savings, while also improving melting yield, suppressing the increase in the amount of slag that becomes waste, and further suppressing wear and tear on the furnace walls. The objective is to provide a steel manufacturing method that can be used with high performance. In order to achieve these objects, the present invention is characterized by including the following steps. That is, in arc furnace steelmaking, (a) oxygen is blown into the furnace during the melting phase, oxidation phase, or both to reduce the carbon content;
obtaining a molten steel of less than 0.20% carbon, preferably less than 0.15%; to be charged. The first step (a) of the operation according to the invention may be carried out in accordance with known methods, for example by charging a raw material such as scrap into a given arc furnace and heating it under normal conditions. All you have to do is arc heating. Further, oxygen gas may be blown in using a normal lance pipe (6 in FIG. 1), and when an auxiliary combustion burner is used, oxygen gas may be blown in in excess of the amount required for combustion of the oil. Note that, as is well known, pure oxygen gas or oxygen-enriched air is preferably used as the oxygen gas to be blown. Moreover, if the situation in the second stage (b) is shown schematically,
As shown in Fig. 1, in the arc furnace 1 there are electrodes (usually three electrodes are used, but only one of them is shown here to simplify the explanation) 2. An arc is generated between the steel and the molten steel 3 to perform heating and refining, and the surface of the molten steel 3 is covered with slag 4. Further, a lance pipe 6 is inserted into the melt in the furnace through a small hole 5 provided at a slag outlet (operation port), and oxygen is blown into the melt through the lance pipe 6. Note that the position of the tip 6A of the lance pipe 6 is normally near the boundary between the molten steel 3 and the molten slag 4, but it may be moved up or down as appropriate depending on the amount of carbon that should be present in the steel and the stage of refining. and transferred into the molten steel 3 or into the slag 4. Furthermore, a refractory container 7 containing hot metal with a high carbon content of about 2% or more is provided on the side of the arc furnace 1, and the container 7 penetrates through the slag outlet (operating port) in the furnace wall. Hot metal is continuously charged into the arc furnace 1 at a predetermined ratio through a refractory gutter 8 that opens into the furnace. If hot metal is continuously charged while continuing arc heating and oxygen injection in this manner, the molten slag 4 will rise as described later. In order to better understand the significance of adopting the above configuration, it seems appropriate to explain the circumstances that led to the establishment of the present invention, so this will be described below. As is well known, the iron oxide content in the molten slag that exists on the molten steel is controlled by the oxygen content (more precisely, the activity) in the molten steel, and the higher the oxygen content in the melt, the more the slag The iron oxide content in it also increases. On the other hand, the oxygen content in molten steel is mainly determined by the carbon content in molten steel under conditions where oxygen supply is sufficient, such as in oxygen-enriched operations. The relationship between carbon content and oxygen content in molten steel has been studied for a long time, and a graph known as the so-called ``Butcher-Hamilton relationship'' is published in various handbooks. According to this, generally the higher the carbon content in molten steel, the lower the oxygen content. Therefore, the iron oxide content in the slag coexisting with the molten steel should also be low. Conversely, a low carbon content in molten steel means a high oxygen content, which results in a high iron oxide content in the slag. When the present inventor attempted to improve the melting yield in the process of exploring oxygen-enriched operations, the first measures he attempted were:
The aim was to adjust the molten steel composition based on the above understanding. In other words, by increasing the amount or selecting the type of carbon additive (pre-carburizer) charged into the arc furnace along with raw materials such as scrap, the carbon content in molten steel can be reduced at the end of oxygen enrichment operation. the oxygen content in the liquid steel at a relatively low level. Adjustment of the carbon content in molten steel using this pre-charged recarburizer is generally effective until the amount of oxygen fed into the furnace is around 5 to 6 Nm 3 /charging ton, and the benefits of oxygen-enriched operation are reduced to some extent. While enjoying the benefits, we were able to somewhat suppress the decrease in melting yield and increase in the amount of slag. However, to obtain the full benefits of oxygen-enriched operation, the oxygen input must be higher. However, when using large amounts of oxygen of 10 Nm 3 /tonne or more, it has been found that it is no longer possible to maintain the carbon content in the molten steel by pre-carburizing. This is because most of the carbon provided by normal charging means is burned away by oxygen, and there is no longer any carbon that can be dissolved in the molten steel. Even if you try to increase the amount of pre-carburized material to an extremely large extent, it may get mixed with the slag that is partially discharged during the refining process and come out of the furnace, or it may be retained in the molten material that sticks to the furnace wall and be used in the subsequent refining process. There is a risk that the metal may fall into the molten steel and interfere with the refining work. In view of this experience, the present invention has been devised to charge hot metal with a high carbon content. The novelty of this method of the present invention is that the carbon content in the molten steel is once lowered to a low level and then carbon is added again. In other words, when carrying out oxygen-enriched operations, we abandon the idea that was conventionally accepted in the art of maintaining the carbon content in molten steel based on the above-mentioned Butcher-Hamilton relationship. A sufficient amount of oxygen gas is injected into the furnace without worrying about the reduction of the carbon content in the iron or the oxidation of the iron content, and the iron oxide produced by combustion is later reduced with carbon to produce metallic iron. The significance of the present invention is that it presents an improvement plan for recovering wastewater as waste. Furthermore, since Hess's law naturally applies to the various chemical reactions that occur in the arc furnace, the heat generated by the oxidation of iron obtained during oxygen-enriched operation is offset by the reduction process of iron oxide. There may be concerns that this may result in When the same amount of oxygen reacts with iron and when it reacts with carbon, Fe+O=FeO+109.6Kcal/mol・O 2 C+O=CO+52.8Kcal/mol・O 2The former generates more heat, but FeO+C→ Due to the endotherm of Fe+CO−56.8Kcal/mol・O 2 , it seemed that only the heat of combustion of carbon could be used in the end. However, as is clear from the examples shown later, the energy saving effect brought about by the oxygen-enriched operation is not diminished by charging hot metal with a high carbon content under arc heating and oxygen injection. The main reason for this is considered to be the foaming of the slag mentioned above. In other words, by introducing carbon through hot metal, iron oxide is reduced and carbon monoxide is produced.
As a result of this foaming the slag with the injected oxygen, the upper part of the foam layer rises by 50cm to 1m when viewed from before the blowing and wraps around the tip of the electrode that is transmitting power, causing the arc to completely bury itself in the slag and generate heat. It is a phenomenon that is highly utilized. Due to the formation of a foam layer on the top of the slag based on this forming phenomenon, this slag foam envelops the arc and also helps keep the molten steel warm, improving the power consumption and shortening the required time. be. Moreover, since the arc is flying in the slag, it is possible to effectively suppress melting of the furnace wall due to the direct effects of the arc, arc noise, and radiant heat from the slag surface. be. In particular, in the case of the present invention, carbon is introduced into the molten steel and slag where the oxygen content is high due to the oxygen enrichment operation in the first stage, so a large amount of carbon monoxide gas is generated. , the above effects become even more pronounced. According to the inventor's experience, the thermal efficiency when heating by electric power without charging hot metal (introducing carbon) after oxygen-enriched operation is approximately 30%; This increases to about 60% when the child gets older. This efficiency increase is, for example, 300 ton in a nominal capacity 70 ton reactor.
This is sufficient to compensate for the endotherm due to the reduction of iron oxide in an example operation in which hot metal containing Kg of carbon is introduced for 5 minutes. Next, a supplementary explanation will be given regarding the configuration of the present invention. The carbon content in molten steel is reduced by blowing oxygen.
Below 0.20%, preferably below 0.15%, and in normal operation below 0.10%, is a condition reached as a result of oxygen-enriched operation rather than being essential to the arc furnace refining process itself. In other words, it is confirmed by the carbon content in the molten steel that a sufficient amount of oxygen has been blown to ensure the benefits of the oxygen-enriched operation. In terms of providing guidance for operations,
This condition has important significance. In terms of actual operation, the amount of oxygen blown to give the above carbon content in molten steel is usually 10 Nm 3 /charging ton or more. These conditions were found empirically by the present inventor in the process of exploring oxygen-enriched operation, and are also supported by the results of decarburization tests in a 70-ton arc furnace. FIG. 2 is a graph showing the relationship between the carbon content in molten steel and the decarburization rate when performing decarburization by oxygen blowing. As is clear from this graph, when the carbon content in molten steel becomes 0.20% or less, more specifically 0.15% or less, the decarburization reaction changes from oxygen supply rate-limiting to carbon diffusion rate-limiting; At this rate, the oxygen supplied into the furnace will primarily oxidize iron. However, according to the present invention, even if the iron content is lost due to oxidation, it is recovered by subsequent carbon injection, so there is no disadvantage at all even if the carbon content of molten steel is reduced to a low value, such as 0.10% or less. do not have. Therefore, oxygen can be blown to the extent that the benefits of oxygen-enriched operation can be sufficiently obtained without worrying about a decrease in carbon content. In addition, the hot metal that is continuously charged into the furnace according to the present invention must contain at least about 2.0% carbon, and if the carbon content is too low, it will not be effective in reducing iron oxide. Therefore, it is difficult to fully achieve the purpose of the present invention. In particular, in the present invention, hot metal produced in a blast furnace or cupola and having a high carbon content of about 3 to 4% or more is advantageously used. Since hot metal is produced in a blast furnace or cupola using coal energy, the overall power consumption in arc furnace steelmaking can be significantly reduced by using such hot metal. While using the carbon component in the hot metal to reduce iron oxide,
This is because the iron component, which is the main component of the hot metal, can be used as it is as the molten steel component of the arc furnace product, and this is a significant feature of the present invention. In other words, the aim of the present invention is to utilize the effect of killing two birds with one stone in that by using the carbon in the hot metal to be removed for reducing iron oxide in arc furnace steelmaking, the hot metal is also converted into molten steel at the same time. By doing so, it is possible to achieve not only a reduction in electric energy in the arc furnace but also a significant improvement in molten steel productivity. In addition, such hot metal should be used so that it will eventually account for 10 to 50% of the total charge (therefore, cold solid materials such as scrap will account for 50 to 90% of the total charge). ), and will be charged into the arc furnace. Further, it is desirable that the charging of the hot metal be carried out at a rate such that the amount of carbon supplied from the hot metal is 0.2 to 2.0 kg/min per ton of molten metal present in the arc furnace. If this charging speed is too slow, the efficiency will be poor, and if it is too fast, problems such as fluctuations in the quality of molten steel are likely to occur when melting is repeated. Furthermore, during such continuous charging of hot metal, arc heating by the electrode 2 continues,
In addition, oxygen gas continues to be blown through the lance pipe 6. Therefore, as the oxygen gas blown in this step (b), the same pure oxygen gas or oxygen-enriched air as in step (a) is used.
Through such arc heating and continuous charging of hot metal under oxygen gas blowing, the above-mentioned effective reduction of iron oxide and the formation of an effective foam layer by the generated carbon monoxide are achieved. By doing so, the excellent effects of the present invention can be achieved. In addition to the specific examples described above, various changes and modifications may be made to the present invention based on the knowledge of those skilled in the art without departing from the spirit of the present invention. Hereinafter, the present invention will be explained in more detail by comparing it with the prior art using an example of steel manufacturing using a UHP arc furnace with a nominal capacity of 70 tons. Comparative Example 1 (Conventional method) 32 tons of commercially purchased scrap, 21 tons of internally generated scrap
1 ton of coke powder and 2 tons of quicklime were charged into an arc furnace, and power transmission (arc heating) was started. After 33 minutes, power transmission was interrupted, and an additional 34 tons of commercially purchased scrap was loaded into the furnace, and power transmission resumed. At 64 minutes after the start of the first power transmission, a portion of the molten steel was collected as a sample for component analysis. The carbon content in the molten steel at this point was 0.25%. Thereafter, 120 Nm 3 of gaseous oxygen was blown into the molten steel using a lance for the purpose of reducing the carbon content in the molten steel (decarburization). After the blowing was completed, a sample for analysis was taken again. The carbon content in the molten steel at this point is
It was 0.08%. After completing the oxygen injection and confirming that the steel bath temperature had reached 1650°C by power transmission (arc heating), samples were taken for analysis again, and then the slag inside the furnace was discharged outside the furnace. The carbon content in the molten steel at this point is
It was 0.06%. According to the analysis of the furnace slag collected at the same time, the iron oxide content in the slag in the furnace at this time was 25%. After discharging the slag, 2.6 tons of elemental alloys were added into the furnace along with quicklime and fluorspar. After these additives were melted by power transmission, it was confirmed that the steel bath temperature had reached 1630℃, and the molten steel in the furnace was tapped into a ladle outside the furnace. The carbon content in the molten steel after tapping was 0.21%.
The weight of molten steel after tapping was 86,200 kg, and therefore the melting yield was 96.2%. The weight of the slag discharged outside the furnace after decarburization and heating was completed was 5.1 tons. The electricity intensity per ton of steel tapped was 510 KWH, which was calculated by dividing the amount of electricity used throughout the entire process by the weight of tapped steel. After tapping is completed, the inside of the arc furnace is repaired with refractories.
After charging the materials for the next melting, power transmission was started 121 minutes after the start of power transmission for the pre-melting. Comparative Example 2 (Oxygen-enriched operation) The same raw materials as in Comparative Example 1 were charged into an arc furnace, and power transmission was started. Ten minutes after the start of power transmission, gaseous oxygen was supplied into the furnace using a lance. 28 minutes after power transmission started, power and air transmission was stopped, 34 tons of commercially purchased scrap was loaded into the furnace, and power transmission resumed. Power transmission resumed 5
After several minutes, gaseous oxygen supply into the furnace was resumed. The operation continued as it was, and samples for analysis were taken when most of the solid charge had entered the steel bath and a smooth surface had been formed. Carbon content in molten steel at this point is 0.10%
It was hot. Thereafter, air was continued to be supplied to the steel bath, and electricity was also transmitted to raise the temperature of the steel bath. After confirming that the steel bath temperature had reached 1650°C, another sample was taken for analysis, and then the molten slag inside the furnace was discharged outside the furnace. The carbon content in the molten steel at this point was 0.04%. According to the analysis of the furnace slag sampled at the same time, the iron oxide content in the furnace slag at this time was 45%. After discharging the slag, the same operation as in Comparative Example 1 was performed to tap the steel into a ladle. The steel melting yield obtained through this operation was 94.5%.
It was hot. The amount of slag discharged outside the furnace was 7.2 tons. The electricity consumption rate was 455KWH/ton of molten steel, and the amount of gaseous oxygen used was 1490Nm3 . One cycle time from the start of power transmission to the start of the next power transmission was 87 minutes. Example: 30 tons of commercially purchased scrap, 20 tons of internally generated scrap
A ton of coke was charged into an arc furnace along with 0.5 ton of coke powder and 2 tons of quicklime, and arc heating was started by power transmission. Approximately 10 minutes after the start of power transmission, gaseous oxygen is blown into the molten steel through a lance into the arc furnace, and the scrap in the furnace is completely melted and the temperature of the molten steel is approximately
After the temperature reached 1500°C, some of the molten steel and slag were collected from inside the furnace as samples for component analysis. At this point, the carbon content in the molten steel was 0.03%, and the iron oxide content in the slag was 53%. While continuing to transmit power and blow gaseous oxygen, 40 tons of molten pig iron at 1350°C with a carbon content of 2.95%, which had been melted and produced in Cupora, was pumped at 2/min.
It was continuously charged into the arc furnace at a speed of 100,000 tons. It took 20 minutes to complete the entire charging of the hot metal, and at the same time the blowing of gaseous oxygen was stopped. The gaseous oxygen required from the start to the end of hot metal charging was 1100Nm3 . Further, shortly after the start of charging the hot metal, the arc noise caused by power transmission became significantly smaller, and the molten slag in the furnace was found to be bubbling and rising to about 1 m. Then, after stopping the oxygen pneumatic supply, the molten steel was heated to 1680°C under power supply, and an analysis sample was collected.
The slag inside the furnace was discharged outside the furnace. The carbon content in the molten steel immediately before slag discharge was 0.1%, and the iron oxide content in the slag was 22%. After discharging the slag, along with quicklime and fluorite, 2.5
After adding tons of element-added alloy into the furnace and melting these additives by power transmission, we confirmed that the molten steel temperature had reached 1630℃ and tapped the molten steel into a ladle outside the furnace. . The amount of molten steel tapped was 89,700 kg.
Therefore, the melting yield is 97% (=89700Kg/92500Kg
Kg). Furthermore, the slag discharged outside the furnace is
It weighed 2.4 tons. The time required from the start of power transmission to the start of power transmission for the next melting was 75 minutes. In addition, the electricity intensity required was
It was 265KWH/ton of molten steel. The above results can be summarized as follows. From this comparison, it can be seen that the arc furnace steelmaking method according to the present invention further significantly improves the level of oxygen-enriched operation in terms of production efficiency and energy cost, and
It is clear that the benefits are high melt yield and low slag emissions.

【表】 1として相対的に比較した。
[Table] 1 for relative comparison.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は本発明の方法の第二段階を説明するた
めの、アーク炉の断面図を中心とする模式的な図
である。第2図は、本発明の方法の第一段階にお
いて、酸素の吹き込みを行なう際の、溶鋼中の炭
素含有率と脱炭速度との関係を示すグラフであ
る。 1:アーク炉、2:電極、3:溶鋼、4:溶融
スラグ、6:ランスパイプ、7:溶銑収容容器、
8:樋。
FIG. 1 is a schematic diagram mainly showing a cross-sectional view of an arc furnace for explaining the second stage of the method of the present invention. FIG. 2 is a graph showing the relationship between carbon content in molten steel and decarburization rate when oxygen is blown in the first step of the method of the present invention. 1: Arc furnace, 2: Electrode, 3: Molten steel, 4: Molten slag, 6: Lance pipe, 7: Hot metal storage container,
8: Gutter.

Claims (1)

【特許請求の範囲】 1 下記の工程を包含することを特徴とするアー
ク炉製鋼法。 (a) 溶解期および/または酸化期に炉内に酸素を
吹き込んで、炭素含量が0.20%以下の溶鋼を得
ること、およびそれに続いて、 (b) アーク加熱並びに酸素の吹込みを行ないつ
つ、少なくとも約2.0%の炭素を含有する溶銑
を連続的に炉内に装入すること。 2 前記工程(a)における酸素の吹込みを、炭素含
量が0.15%以下の溶鋼を得るように行なう特許請
求の範囲第1項記載の製鋼法。 3 前記溶銑の装入を該溶銑から供給される炭素
量が炉内に存在する溶融物1トン当り0.2〜2.0
Kg/分となる割合で、行なう特許請求の範囲第1
項記載の製鋼法。 4 前記溶銑が、全装入物の10〜50%の割合とな
るように、装入せしめられる特許請求の範囲第1
項記載の製鋼法。 5 前記溶銑が、溶鉱炉またはキユポラで予め製
造されたものである特許請求の範囲第1項乃至第
4項のいずれかに記載の製鋼法。 6 前記工程(a)並びに(b)における酸素の吹込み
が、純酸素ガスまたは酸素富化空気を用いて行な
われる特許請求の範囲第1項記載の製鋼法。 7 前記工程(a)における酸素の吹込み量が、純酸
素ガス換算で少なくとも10Nm3/装入トンである
特許請求の範囲第1項記載の製鋼法。
[Scope of Claims] 1. An arc furnace steelmaking method characterized by including the following steps. (a) blowing oxygen into the furnace during the melting phase and/or oxidation phase to obtain molten steel with a carbon content of 0.20% or less, and (b) while performing arc heating and blowing oxygen, Continuously charging hot metal containing at least about 2.0% carbon into the furnace. 2. The steel manufacturing method according to claim 1, wherein the oxygen injection in step (a) is carried out to obtain molten steel having a carbon content of 0.15% or less. 3 Charge the hot metal so that the amount of carbon supplied from the hot metal is 0.2 to 2.0 per ton of molten metal present in the furnace.
Kg/min.
Steel manufacturing method described in section. 4. Claim 1, wherein the hot metal is charged at a rate of 10 to 50% of the total charge.
Steel manufacturing method described in section. 5. The steel manufacturing method according to any one of claims 1 to 4, wherein the hot metal is produced in advance in a blast furnace or cupola. 6. The steel manufacturing method according to claim 1, wherein the oxygen injection in steps (a) and (b) is performed using pure oxygen gas or oxygen-enriched air. 7. The steel manufacturing method according to claim 1, wherein the amount of oxygen blown in step (a) is at least 10 Nm 3 /charging ton in terms of pure oxygen gas.
JP9656980A 1980-07-15 1980-07-15 Arc furnace steel making method Granted JPS5723016A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9656980A JPS5723016A (en) 1980-07-15 1980-07-15 Arc furnace steel making method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9656980A JPS5723016A (en) 1980-07-15 1980-07-15 Arc furnace steel making method

Publications (2)

Publication Number Publication Date
JPS5723016A JPS5723016A (en) 1982-02-06
JPS635450B2 true JPS635450B2 (en) 1988-02-03

Family

ID=14168631

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9656980A Granted JPS5723016A (en) 1980-07-15 1980-07-15 Arc furnace steel making method

Country Status (1)

Country Link
JP (1) JPS5723016A (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105087861A (en) * 2015-09-02 2015-11-25 共享铸钢有限公司 Method for smelting primary steel making liquid for high-alloy steel casting
JP7128602B1 (en) * 2022-03-11 2022-08-31 山田 榮子 Scrap metal melting method with less industrial waste

Also Published As

Publication number Publication date
JPS5723016A (en) 1982-02-06

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