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JPH0313291B2 - - Google Patents
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JPH0313291B2 - - Google Patents

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Publication number
JPH0313291B2
JPH0313291B2 JP57078120A JP7812082A JPH0313291B2 JP H0313291 B2 JPH0313291 B2 JP H0313291B2 JP 57078120 A JP57078120 A JP 57078120A JP 7812082 A JP7812082 A JP 7812082A JP H0313291 B2 JPH0313291 B2 JP H0313291B2
Authority
JP
Japan
Prior art keywords
furnace
ore
reduction furnace
hearth
smelting
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 - Lifetime
Application number
JP57078120A
Other languages
Japanese (ja)
Other versions
JPS58197208A (en
Inventor
Mitsuo Kadoto
Nobuo Tsuchitani
Hisao Hamada
Hisamitsu Koitabashi
Toshihiro Inatani
Shiko Takada
Eiji Katayama
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 JP57078120A priority Critical patent/JPS58197208A/en
Publication of JPS58197208A publication Critical patent/JPS58197208A/en
Publication of JPH0313291B2 publication Critical patent/JPH0313291B2/ja
Granted legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21BMANUFACTURE OF IRON OR STEEL
    • C21B13/00Making spongy iron or liquid steel, by direct processes
    • C21B13/0006Making spongy iron or liquid steel, by direct processes obtaining iron or steel in a molten state
    • C21B13/0013Making spongy iron or liquid steel, by direct processes obtaining iron or steel in a molten state introduction of iron oxide into a bath of molten iron containing a carbon reductant
    • C21B13/002Reduction of iron ores by passing through a heated column of carbon
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21BMANUFACTURE OF IRON OR STEEL
    • C21B2100/00Handling of exhaust gases produced during the manufacture of iron or steel
    • C21B2100/60Process control or energy utilisation in the manufacture of iron or steel
    • C21B2100/66Heat exchange

Landscapes

  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Manufacture And Refinement Of Metals (AREA)
  • Manufacture Of Iron (AREA)

Description

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

本発明は金属酸化物の溶融還元法に関するもの
である。 近年金属酸化物を含有する鉱石資源は塊状のも
のが減少し、粉粒状のものが増加する傾向にあ
る。ここような粉粒状鉱石は多くの場合塊成化さ
れてから、通常の塊状鉱石と同様に溶解炉で製練
されている。これら溶解炉として電気炉、転炉あ
るいはその他の溶解炉が使用されている。さらに
また前記塊成化された鉱石を予備還元した後に上
記各種の溶解炉で溶融還元して、電力消費ならび
にエネルギーコストの低減が計られる場合もあ
る。しかしながら電気炉以外の転炉・その他の溶
融炉を用いて難溶性、難還元性の鉱石、例えばク
ロム鉱の予備還元鉱を溶融還元することは操業が
非常に困難であるという欠点があり、一方塊成化
鉱を予備還元した後電気炉で溶融還元する方法は
製造方法としては最も安定した操業方法であり、
従来例えばクロム粉状鉱をペレツトとなし、ロー
タリーキルン中で予備還元した予備還元ペレツト
をサブマージアーク式電気炉中で溶融還元してフ
エロクロムの生産が行なわれている。 しかしながら、粉粒状鉱石を塊成化処理するに
はその処理コストが多大であり、また塊成化鉱を
予備還元したとしても電気炉中において溶融還元
するための電力エネルギーはなお多大であり、塊
成化処理コストならびに電力消費コスト上から経
済性が圧迫されるという欠点があつた。 本発明者らは、製造コストの抵減、なかでも電
力エネルギー使用を脱却することを目的として、
粉粒状鉱石を直接使用して各種溶融金属を製造す
る方法として予備還元炉と炭素系固体還元剤充填
層が形成された溶融還元炉とを使用する溶融還元
方法を発明し、特願昭56−63294号により先に特
許出願した。前記方法は予備還元炉と溶融還元炉
を用いて、前記溶融還元炉からの排ガスを前記予
備還元炉に吹込んで粉粒状鉱を予備還元した後、
予備還元鉱を溶融還元炉の下部に上下2段にそれ
ぞれ設けられた複数の羽口のうち少なくとも上段
の羽口から供給して、溶融還元炉に形成された充
填層の固体還元剤と羽口から吹込まれる熱風およ
びまたは酸素富化空気によつて溶融還元して炉床
に蓄溜された溶融金属をスラグと共に適時排出す
るという方法である。 ところで、前記方法を実施する試験炉での実験
によれば、上段羽口から予備還元鉱石とフラツク
スを吹込んだ場合予備還元鉱石はフラツクスと共
に羽口の先端近傍に形成される高温域において溶
融し、固体還元剤によつて形成されている充填層
を滴下する際に溶融還元が促進され、金属とスラ
グの分離が進行しながら溶融した金属とスラグが
炉床に蓄溜される。この際例えばクロム鉱を製錬
する場合には溶融金属の成分組成中Siは4〜9
%、Sは0.1〜0.5%、Pは0.1〜0.4%、Cは3〜
7%、残部は実質的に主成分たる金属元素Cr、
Feであり、溶融金属中のSiもしくはその他の元
素の含有量を所定量に調整するためには、溶融還
元炉から排出した後、別の炉で再精錬する必要が
ある。さらにまた種々の要因により操業が不安定
となつて熱供給不足あるいは炉床に至るまでの間
の製錬反応が不十分な条件の下では、排出溶融ス
ラグ中に、例えばクロム鉱を製錬する場合には、
Cr、Feが未還元酸化物状態で増加し、また溶融
金属、溶融スラグの流動性が低下して、これら溶
融物を排出させることが困難となることがある。
このように一旦製錬不足あるいは熱不足の状態で
溶融物が炉床に至つた場合には、例えば送風温度
を上昇させるなど採り得る対策には限界があり、
十分な効果を得ることはできなかつた。 本発明は、本発明者らが先に出願した前記発明
の有する欠点を除去、改良することのできる金属
酸化物の溶融還元法を提供することを目的とする
ものであり、特許請求の範囲記載の方法を提供す
ることによつて前記目的を達成することができ
る。すなわち本発明は炭素系固体還元剤により形
成される充填層を有する竪型溶融還元炉より排出
される高温排ガスを予備還元炉に導入し、一方粉
粒状鉱石を前記予備還元炉に装入して流動予備還
元して得られる予備還元鉱石を前記溶融還元炉の
羽口から吹込むことによる粉粒状金属酸化鉱石の
溶融還元方法において、複数の吹込み装置が炉床
部に設けられた溶融還元炉の炉床湯溜部に蓄溜さ
れている溶融金属浴または溶融スラグ浴の何れか
少なくとも1つの浴中に前記吹込み装置を経て固
体、気体、液体の何れか少なくとも1つの状態の
各種精錬剤あるいは昇温剤を直接吹込んで炉床に
おいて各種精錬反応およびまたは昇温反応を促進
させながら溶融金属ならびに溶融スラグの成分組
成の調整と温度制御を行なつた後に溶融還元炉か
らの排出させることを特徴とする金属酸化鉱石の
溶融還元方法に関するものである。 次に本発明を1つの実施態様例について図面を
参照して説明する。 溶融還元炉1は竪型の炉であつて、炉内には炭
素系固体還元剤からなる充填層が形成されてお
り、前記還元剤は通常炉頂に設けられた還元剤供
給口2より炉内に供給される。溶融還元炉1内で
発生する高温の還元性排ガスは排出口3より予備
還元炉4の下部に設けられた供給口5を経て予備
還元炉4内に供給され、同炉4内において粉粒状
鉱石を流動還元によつて予備還元する機能を果
す。なおこの際必要によりフラツクスも同炉4内
に供給される。予備還元炉4に設けられた予備還
元排出口6から排出される予備還元鉱とフラツク
スは輸送されて溶融還元炉1に上下2段にそれぞ
れ設けられた複数の羽口7から同炉1内に高温空
気およびまたは酸素富化空気と共に吹込まれる。
このように羽口7から吹込まれた鉱石とフラツク
スは炉内の羽口先端近傍の高温部で溶融し、さら
に滴下しながら溶融還元されて炉床に蓄溜する際
に溶融スラグと溶融金属の2相に分離する。羽口
レベルより下方の炉床には炉床に蓄溜される溶融
物にその先端が浸漬するよう複数本の炉床吹込み
管8が炉殻を斜目に貫通して設けられており、前
記吹込み管8を経て固体、気体、液体のうちから
選ばれる何れか少なくとも1つの状態の各種精錬
剤、昇温剤が溶融した金属浴9およびまたはスラ
グ浴10中に吹込まれる。その際吹込み管先端の
位置を適宜移動させることができる。このように
して成分調整された溶融金属およびスラグはタツ
プホール11から注出される。 次に気体、固体精錬剤による精錬反応の数例に
ついて、反応式(1)〜(4)を示す。 〔Si〕+O2=SiO2 ……(1) 〔S〕+CaC2=(CaS)+2C ……(2) (Cr2O3)+3C=2〔Cr〕+3CO ……(3) (FeO)+C=〔Fe〕+CO ……(4) ところで、液体精錬剤としては種々の金属元素
の合金系の溶融金属があり、これら液体を前記炉
床吹込み管8を経て注入することによつても炉床
に蓄溜されている溶融金属の成分を調整すること
ができる。なお昇温剤としてはアルミニウム系な
どのテルミツト剤を用いることができる。上記
種々の精錬剤、昇温剤を単独でもしくは組合せて
使用した実験結果によれば、炉床における精錬反
応および昇温反応により、溶融した金属およびま
たはスラグの成分組成ならびに流動性を容易に制
御することができることが判つた。 次に本発明を、試験炉を用いて行つた実施例に
ついて説明する。 実施例 (1) 原料:予備還元クロム鉱石、供給量 360
Kg/h 予備還元率 35% 粒度分布 50〜100mesh(80%) (2) フラツクス:供給量 180Kg/h けい石、石灰 (3) 炭素系固体還元剤の種類:コークス、供給量
600Kg/h 粒度分布 15〜30mm (4) 竪型炉への送風量:1250Nm3/h 送風温度 800〜900℃ 送風羽口 上下各4本 計8本 (上段4本に予備還元クロム鉱石とフラツク
スを供給) (5) 溶融金属生産量:245Kg/h (6) 溶融スラグ排出量:340Kg/h (7) 実験結果
The present invention relates to a method for melting and reducing metal oxides. In recent years, there has been a tendency for ore resources containing metal oxides to be less in the form of lumps and more in the form of powder. Such granular ores are often agglomerated and then smelted in a melting furnace in the same way as ordinary lump ores. As these melting furnaces, electric furnaces, converters, or other melting furnaces are used. Furthermore, the agglomerated ore may be pre-reduced and then melted and reduced in the various melting furnaces described above to reduce power consumption and energy costs. However, using a converter or other melting furnace other than an electric furnace to melt and reduce ores that are difficult to melt and hard to reduce, such as pre-reduced ores of chromite, has the drawback that the operation is extremely difficult. The method of pre-reducing agglomerate ore and then melting and reducing it in an electric furnace is the most stable production method.
Conventionally, ferrochrome has been produced by making chromium powder ore into pellets, pre-reducing the pellets in a rotary kiln, and then melting and reducing the pre-reduced pellets in a submerged arc electric furnace. However, processing costs to agglomerate powdery ore are large, and even if the agglomerated ore is pre-reduced, the electric energy required to melt and reduce it in an electric furnace is still large, and The disadvantage was that economic efficiency was put under pressure due to chemical treatment costs and power consumption costs. The inventors of the present invention aimed to reduce manufacturing costs, and in particular to eliminate the use of electrical energy.
As a method for producing various molten metals by directly using powdered ore, he invented a smelting reduction method that uses a preliminary reduction furnace and a smelting reduction furnace in which a carbon-based solid reducing agent packed bed was formed, and he filed a patent application in 1983- A patent application was previously filed under No. 63294. The method uses a preliminary reduction furnace and a smelting reduction furnace, and after blowing exhaust gas from the smelting reduction furnace into the preliminary reduction furnace to preliminary reduce the granular ore,
Pre-reduced ore is supplied from at least the upper tuyere of the plurality of tuyeres provided in two upper and lower stages in the lower part of the smelting reduction furnace, and the solid reducing agent and tuyere of the packed bed formed in the smelting reduction furnace are supplied. In this method, the molten metal accumulated in the hearth is melted and reduced by hot air and/or oxygen-enriched air blown from the furnace, and the molten metal accumulated in the hearth is discharged together with the slag in a timely manner. By the way, according to experiments in a test furnace implementing the above method, when pre-reduced ore and flux are injected from the upper tuyere, the pre-reduced ore melts together with the flux in the high temperature region formed near the tip of the tuyere. When the packed bed formed by the solid reducing agent is dropped, the melting reduction is promoted, and the molten metal and slag are accumulated in the hearth as separation of the metal and slag progresses. At this time, for example, when smelting chrome ore, Si in the composition of the molten metal is 4 to 9.
%, S is 0.1~0.5%, P is 0.1~0.4%, C is 3~
7%, the remainder being essentially the main component, the metallic element Cr;
It is Fe, and in order to adjust the content of Si or other elements in the molten metal to a predetermined amount, it is necessary to re-smelt it in another furnace after discharging it from the smelting reduction furnace. Furthermore, under conditions where the operation becomes unstable due to various factors and the heat supply is insufficient or the smelting reaction leading to the hearth is insufficient, it is necessary to smelt, for example, chromium ore into the discharged molten slag. in case of,
Cr and Fe increase in the unreduced oxide state, and the fluidity of the molten metal and molten slag decreases, making it difficult to discharge these molten materials.
Once the molten material reaches the hearth with insufficient smelting or heat, there are limits to the measures that can be taken, such as increasing the temperature of the blast.
It was not possible to obtain sufficient effect. The present invention aims to provide a method for melting and reducing metal oxides that can eliminate and improve the drawbacks of the invention previously filed by the present inventors, and the scope of the claims is as follows: The above object can be achieved by providing a method. That is, the present invention introduces high-temperature exhaust gas discharged from a vertical smelting reduction furnace having a packed bed formed of a carbon-based solid reducing agent into a pre-reduction furnace, and charges granular ore into the pre-reduction furnace. A smelting reduction method for granular metal oxide ore by blowing pre-reduced ore obtained by fluidized pre-reduction through the tuyere of the smelting reduction furnace, in which a plurality of blowing devices are provided in the hearth part. Various refining agents in at least one state of solid, gas, or liquid are passed through the blowing device into at least one of the molten metal bath and the molten slag bath stored in the hearth sump. Alternatively, a heating agent may be directly injected to promote various refining reactions and/or temperature raising reactions in the hearth, while adjusting the composition and temperature of the molten metal and molten slag, and then discharging the molten metal and molten slag from the smelting reduction furnace. The present invention relates to a characteristic method for melting and reducing metal oxide ores. Next, one embodiment of the present invention will be described with reference to the drawings. The melting reduction furnace 1 is a vertical furnace, and a packed bed made of a carbon-based solid reducing agent is formed in the furnace, and the reducing agent is normally supplied to the furnace through a reducing agent supply port 2 provided at the top of the furnace. supplied within. High-temperature reducing exhaust gas generated in the smelting reduction furnace 1 is supplied from the exhaust port 3 to the preliminary reduction furnace 4 via the supply port 5 provided at the lower part of the preliminary reduction furnace 4, and in the same furnace 4, powdered ore is produced. The function is to preliminarily reduce the amount by fluid reduction. At this time, flux is also supplied into the furnace 4 if necessary. The pre-reduced ore and flux discharged from the pre-reduction discharge port 6 provided in the pre-reduction furnace 4 are transported into the melting reduction furnace 1 through a plurality of tuyeres 7 provided in two upper and lower stages, respectively. Blown with hot air and/or oxygen-enriched air.
The ore and flux injected from the tuyere 7 melt in the high temperature area near the tip of the tuyere in the furnace, and are further melted and reduced as they drip, forming molten slag and molten metal as they accumulate in the hearth. Separates into two phases. In the hearth below the tuyere level, a plurality of hearth blowing pipes 8 are provided diagonally penetrating the hearth shell so that their tips are immersed in the molten material stored in the hearth. Various refining agents and temperature increasing agents in at least one state selected from solid, gas, and liquid are blown into the molten metal bath 9 and/or slag bath 10 through the blowing pipe 8. At this time, the position of the tip of the blowing tube can be moved as appropriate. The molten metal and slag whose composition has been adjusted in this way are poured out from the taphole 11. Next, reaction formulas (1) to (4) are shown for several examples of refining reactions using gaseous and solid refining agents. [Si] + O 2 = SiO 2 ... (1) [S] + CaC 2 = (CaS) + 2C ... (2) (Cr 2 O 3 ) + 3C = 2 [Cr] + 3CO ... (3) (FeO) + C =[Fe]+CO...(4) By the way, liquid refining agents include molten metals based on alloys of various metal elements, and these liquids can also be injected into the furnace by injecting them through the hearth injection pipe 8. The composition of the molten metal stored in the bed can be adjusted. Note that as the temperature increasing agent, a thermite agent such as an aluminum type can be used. According to experimental results using the various refining agents and temperature raising agents mentioned above, either singly or in combination, the composition and fluidity of molten metal and/or slag can be easily controlled by the refining reaction and temperature raising reaction in the hearth. It turns out that it can be done. Next, an example in which the present invention was carried out using a test furnace will be described. Example (1) Raw material: Pre-reduced chromium ore, supply amount 360
Kg/h Preliminary reduction rate 35% Particle size distribution 50-100mesh (80%) (2) Flux: Supply amount 180Kg/h Silica stone, lime (3) Type of carbon-based solid reducing agent: Coke, supply amount
600Kg/h Particle size distribution 15~30mm (4) Amount of air blown to the vertical furnace: 1250Nm 3 /h Air temperature 800~900℃ Air tuyeres 4 each on the upper and lower sides, 8 in total (pre-reduced chromium ore and flux are placed in the upper 4) (5) Molten metal production: 245Kg/h (6) Molten slag discharge: 340Kg/h (7) Experimental results

【表】 以上実施例より判るように、本発明によれば、
精錬剤あるいは昇温剤を炉床内に蓄溜された溶融
物中に吹込むことにより、炉床部において溶融金
属および溶融スラグの成分調整を行むうことがで
き、かつ溶融物を流動性も制御することができる
ので、溶融物の排出作業のトラブルが解消した。 本発明の効果をまとめると次のようになる。 炉床部に溜つている溶融金属あるいは溶融スラ
グ浴中へ直接精錬剤、昇温剤を吹込むことによつ
て、炉床で精錬反応、昇温反応を促進させること
ができるので、次の利点がある。 (1) 炉外での溶融金属の精錬時間が大幅に短縮さ
れる。 (2) スラグ中金属酸化物の還元率の向上によつて
生産率が増加する。 (3) 溶融物の流動性不良による出銑、出滓のトラ
ブルが解消できる。
[Table] As can be seen from the examples above, according to the present invention,
By injecting a refining agent or a temperature raising agent into the molten material stored in the hearth, it is possible to adjust the composition of the molten metal and molten slag in the hearth, and also improve the fluidity of the molten material. Since it can be controlled, the trouble of discharging the melted material has been solved. The effects of the present invention can be summarized as follows. By injecting the refining agent and temperature raising agent directly into the molten metal or molten slag bath accumulated in the hearth, the refining reaction and temperature raising reaction can be accelerated in the hearth, resulting in the following advantages: There is. (1) The time for refining molten metal outside the furnace is significantly reduced. (2) Production rate increases by improving the reduction rate of metal oxides in slag. (3) Problems with iron tapping and slag due to poor fluidity of the molten material can be resolved.

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

図は本発明の実施態様の1例の系統図である。 1……溶融還元炉、2……還元剤供給口、3…
…排ガス排出口、4……予備還元炉、5……ガス
供給口、6……予備還元鉱排出口、7……羽口、
8……炉床吹込み管、9……溶融金属浴、10…
…溶融スラグ浴、11……タツプホール。
The figure is a system diagram of one example of an embodiment of the present invention. 1... Melting reduction furnace, 2... Reducing agent supply port, 3...
...Exhaust gas discharge port, 4...Preliminary reduction furnace, 5...Gas supply port, 6...Preliminary reduction ore discharge port, 7...Tuyere,
8... Hearth blowing pipe, 9... Molten metal bath, 10...
...molten slag bath, 11...tap hole.

Claims (1)

【特許請求の範囲】[Claims] 1 炭素系固体還元剤により形成される充填層を
有する竪型溶融還元炉より排出される高温排ガス
を予備還元炉に導入し、一方粉粒状鉱石を前記予
備還元炉に装入して流動予備還元して得られる予
備還元鉱石を前記溶融還元炉の羽口から吹込むこ
とによる粉粒状金属酸化鉱石の溶融還元方法にお
いて、複数の吹込み装置が炉床部に設けられた溶
融還元炉の炉床湯溜部に蒸溜されている溶融金属
浴または溶融スラグ浴の何れか少なくとも1つの
浴中に前記吹込み装置を経て固体、気体、液体の
何れか少なくとも1つの状態の各種精錬剤あるい
は昇温剤を直接吹込んで炉床において各種精錬反
応およびまたは昇温反応を促進させながら溶融金
属ならびに溶融スラグの成分組成の調整と温度制
御を行なつた後に溶融還元炉から排出させること
を特徴とする金属酸化鉱石の溶融還元方法。
1. High-temperature exhaust gas discharged from a vertical smelting reduction furnace having a packed bed formed by a carbon-based solid reducing agent is introduced into a pre-reduction furnace, and on the other hand, granular ore is charged into the pre-reduction furnace for fluidized pre-reduction. A hearth of a smelting reduction furnace in which a plurality of blowing devices are provided in the hearth in a method for smelting and reducing powdery metal oxide ore by blowing pre-reduced ore obtained through the tuyeres of the smelting and reducing furnace. Various refining agents or temperature increasing agents in at least one of solid, gas, and liquid states are passed through the blowing device into at least one of the molten metal bath and molten slag bath distilled in the sump. A metal oxidation method characterized by directly injecting molten metal and molten slag to promote various refining reactions and/or temperature raising reactions in the hearth, adjusting the composition of the molten metal and molten slag, and controlling the temperature, and then discharging from the smelting reduction furnace. Method for melting down ore.
JP57078120A 1982-05-12 1982-05-12 Melt reduction method of metallic oxide ore Granted JPS58197208A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57078120A JPS58197208A (en) 1982-05-12 1982-05-12 Melt reduction method of metallic oxide ore

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57078120A JPS58197208A (en) 1982-05-12 1982-05-12 Melt reduction method of metallic oxide ore

Publications (2)

Publication Number Publication Date
JPS58197208A JPS58197208A (en) 1983-11-16
JPH0313291B2 true JPH0313291B2 (en) 1991-02-22

Family

ID=13653020

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57078120A Granted JPS58197208A (en) 1982-05-12 1982-05-12 Melt reduction method of metallic oxide ore

Country Status (1)

Country Link
JP (1) JPS58197208A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60218407A (en) * 1984-04-13 1985-11-01 Nippon Tekko Renmei Method for operating melt reducing system
DE3540037A1 (en) * 1984-07-10 1987-01-08 Kuettner Gmbh & Co Kg Dr Process and apparatus for feeding lime into shaft furnaces

Also Published As

Publication number Publication date
JPS58197208A (en) 1983-11-16

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