JPS62158814A - Composite refining agent and refining method - Google Patents

Composite refining agent and refining method

Info

Publication number
JPS62158814A
JPS62158814A JP61000262A JP26286A JPS62158814A JP S62158814 A JPS62158814 A JP S62158814A JP 61000262 A JP61000262 A JP 61000262A JP 26286 A JP26286 A JP 26286A JP S62158814 A JPS62158814 A JP S62158814A
Authority
JP
Japan
Prior art keywords
weight
agent
refining
calcium
refining agent
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.)
Granted
Application number
JP61000262A
Other languages
Japanese (ja)
Other versions
JPH0364566B2 (en
Inventor
Yuji Hanada
花田 裕司
Motomichi Yoshino
能野 基道
Naohiko Kusano
草野 尚彦
Takeshi Nakamura
毅 中村
Kunio Nomura
野村 邦雄
Shingo Ito
信吾 伊藤
Yasunobu Watanabe
渡辺 泰亘
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.)
Topy Industries Ltd
Yahashi Kogyo KK
Original Assignee
Topy Industries Ltd
Yahashi Kogyo KK
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 Topy Industries Ltd, Yahashi Kogyo KK filed Critical Topy Industries Ltd
Priority to JP61000262A priority Critical patent/JPS62158814A/en
Publication of JPS62158814A publication Critical patent/JPS62158814A/en
Publication of JPH0364566B2 publication Critical patent/JPH0364566B2/ja
Granted legal-status Critical Current

Links

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

Abstract

PURPOSE:To manufacture a composite refining agent for secondary steel refining excellent in meltability and reactivity by blending uniformly specific percentage of respectively powdered or granular materials of quick lime, fluorite, calcium carbide, deoxidizers, and carbon and by compacting the resulting mixture. CONSTITUTION:The mixture containing, by weight, >=50% quick lime, 5-20% fluorite, and <=10% calcium carbide and also containing deoxidizers and carbon in the amounts specfied by inequalities [C]<6, (CaO)/(SiO2)> 2.3, and 0.4[Ca]+1.4[Si]+1.33[C]>9 is prepared. In the above inequalities, [C] means the sum of raw-material carbon quantities ]wt%]; (CaO) and (SiO2) mean, severally, the total amounts of Ca and Si expressed in terms of CaO and SiO2, respectively [wt%]; [Ca] means the sum of Ca content in CaC2 and calcium silicon [wt%]; and [Si] means the sum of Si content in silicon carbide, calcium silicon, and ferrosilicon [wt%]. The above components (about 10-20mm grain size) are crushed to <= about 5mm and mixed uniformly, and the resulting mixture is compacted into spherical shape of about 10-20mm so as to be formed into acomposite refining agent.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 近年鋼の溶製において、溶解や粗精練した溶鋼を、粗精
錬の酸化性スラグと分離し、別の炉外精錬設備に移して
脱酸剤や造滓剤等を加え、還元や脱硫を行う精錬方法が
広〈実施されている。この場合前工程でのスラグを炉外
精錬工程に持込ないことが必要であるが、適切な脱酸剤
や造滓剤を選択して使用することも又重要である。本発
明は上記の溶鋼の炉外精錬(以下二次精錬と定義する)
に際して溶鋼に添加する、脱酸剤と造滓剤の性質を兼ね
備えた複合精錬剤に関する。
[Detailed Description of the Invention] [Industrial Application Field] In recent years, in steel refining, molten steel that has been melted or roughly refined is separated from the oxidizing slag of the rough refining, and transferred to a separate outside furnace refining equipment to be deoxidized. Refining methods that involve adding additives and slag-forming agents to perform reduction and desulfurization are widely practiced. In this case, it is necessary not to bring the slag from the previous process into the external refining process, but it is also important to select and use an appropriate deoxidizer or slag forming agent. The present invention relates to the above-mentioned out-of-furnace refining (hereinafter defined as secondary refining) of the molten steel.
This invention relates to a composite refining agent that has the properties of both a deoxidizing agent and a slag-forming agent, and is added to molten steel during processing.

〔従来の技術〕[Conventional technology]

二次精錬で溶鋼に添加する材料は、生石灰、フラックス
及び脱酸剤であり、従来それ等の使用方法は単味あるい
は混合して使用されていた。即ち混合使用方法は次の様
に区分されていた。
The materials added to molten steel in secondary refining are quicklime, flux, and deoxidizer, and conventionally these have been used singly or in combination. In other words, the mixed usage methods were classified as follows.

イ、生石灰+フラックス系の造滓剤 口、スラグの流動性及び滓化性を改善した補助造滓剤的
なスラグ調整剤 ハ、スラグ調整剤に補助脱酸剤(CaCZ。
(a) A slag forming agent with a quicklime + flux system; a slag conditioner as an auxiliary slag forming agent that improves the fluidity and slag formation of slag; (c) an auxiliary deoxidizing agent (CaCZ) as a slag conditioner.

SiC,Fe−5i等)を加えた還元脱酸造滓剤だあっ
たが、その形態は粉粒混合物並びに造粒物であり、又還
元精錬に必要な総ての能力を備えた(以下ワンタッチ式
と定義する)ワンタッチ式精錬剤でないため以下の欠点
があった。即ち、精錬剤の種類が複雑になり、ホッパー
ならびに投入設備等が煩雑となりハンドリングの負荷が
大きく、又粉粒状混合物ではハンドリング中に振動など
で原料構成成分の分離が起り均質性を損い、またワンタ
ッチ式精錬剤と比較して操炉熟練度が必要であった。
SiC, Fe-5i, etc.) was added as a reducing deoxidizing slag agent, but its form was a powder mixture and granules, and it also had all the capabilities necessary for reduction refining (hereinafter referred to as one-touch slag). Since it is not a one-touch refining agent (defined as a formula), it has the following drawbacks. In other words, the types of refining agents become complicated, the hopper and charging equipment become complicated, and the handling load becomes large.In addition, in the case of powdery mixtures, the raw material components are separated due to vibrations during handling, which impairs homogeneity. Compared to the one-touch refining agent, it required more skill in furnace operation.

また生石灰やフラックスや脱酸剤を単味で使用する際は
、溶融を早め反応性をよくするために粉体での添加が望
ましいが、キャリアガス等による吹込の方法は大規模な
設備が必要であり、また粉体を溶鋼に直接添加するには
別個の集塵装置等が必要なために普遍的ではな(、従っ
て従来の添加物は塊状の副原料や合金鉄が主であり、特
別の工夫は払われていなかった。
Also, when using quicklime, flux, or deoxidizing agent alone, it is desirable to add it in powder form to speed up melting and improve reactivity, but blowing with carrier gas requires large-scale equipment. Moreover, adding powder directly to molten steel requires a separate dust collector, so it is not universally used. No effort was made to do so.

〔発明が解決しようとする問題点〕[Problem that the invention seeks to solve]

本発明は、二次精錬の溶鋼えの添加物であって、迅速に
溶融して反応性がよく、添加に際して粉塵の発生が少な
く、互生たる添加物を適切な割合で全て複合させたワン
タッチ式の二次精錬用の精錬剤の製造を目的としており
、またこの精錬剤を用いて効率よ(二次精錬を行うこと
を目的としている。
The present invention is an additive for secondary refining molten steel, which melts quickly and has good reactivity, generates little dust when added, and is a one-touch type that combines all alternating additives in an appropriate ratio. The purpose is to produce a refining agent for secondary refining, and to perform secondary refining efficiently using this refining agent.

〔問題点を解決するための手段〕[Means for solving problems]

本発明は、生石灰が50重量%以上、螢石が5−20重
量%、炭化カルシウムが10重量%以下でかつ下記の第
(1)〜(3)式で規定される量の脱酸剤及び炭素を含
有する混合物であって、各成分を粉粒物とし、均一に混
合したあと加圧成形しあるいはバインダーを用いて造粒
成形した複合精錬剤であり父上記の原料に熱崩壊剤とし
て蛭石、真珠岩、黒曜石、松脂石、膨張頁岩の1種若し
くは2種以上を5重量%以下の量加えた混合物であって
、各成分原料を粉粒物とし、均一に混合したあと加圧成
形加工によりあるいはバインダーを用いて造粒成形した
熱崩壊型の複合精錬剤であり、更には上記の複合精錬剤
又は熱崩壊型の複合精錬剤を炉外精錬用の受鋼槽内に予
め入れ置し、これにスラグを分離した溶鋼を受綱し、受
鋼時の溶鋼流の強力な攪拌力により短時間で脱酸、造滓
および脱流を行うことを特徴とする溶鋼の二次精錬法で
ある。
The present invention provides a deoxidizing agent containing 50% by weight or more of quicklime, 5-20% by weight of fluorite, 10% by weight or less of calcium carbide, and an amount specified by the following formulas (1) to (3). It is a composite refining agent that is a mixture containing carbon, in which each component is made into powder and granules, mixed uniformly and then pressure molded or granulated using a binder. A mixture containing one or more of stone, nacre, obsidian, pinestone, and expanded shale in an amount of 5% by weight or less, in which each component raw material is made into powder and granules, mixed uniformly, and then pressure-molded. It is a heat-collapse type composite refining agent that is granulated by processing or using a binder, and the above-mentioned composite refining agent or heat-collapse type composite refining agent is placed in advance in a steel receiving tank for out-of-furnace refining. A secondary refining method for molten steel, which is characterized in that molten steel from which slag has been separated is fed into the molten steel, and deoxidized, slag-formed, and deflowed in a short time by the strong stirring force of the molten steel flow during steel receiving. It is.

(C) < 6  −−−−−−−−−−−−−・・・
−・・・・−・−−−−−−−−(1)但しくC)は原
料の炭素量の合計(重量%)(CaO) /  (S 
i Oz ) > 2.3−−−−−−  (2)但し
くCa O)は原料中のCaの全量をCaOに、又(S
iO□)はStの全量を5i02に換算した重量% 0.4  (Ca) + 1.14 (St) + 1
.33 (C) > 9 −(3)但し〔Ca〕は炭化
カルシウム、カルシウムシリコン中のカルシウム分の合
計(重量%)、C3i)は炭化珪素、カルシウムシリコ
ン、フェロシリコン中の珪素分の合計(重量%)である
(C) < 6 −−−−−−−−−−−−−・・・・
−・・−・−−−−−−−−(1) However, C) is the total amount of carbon in the raw materials (wt%) (CaO) / (S
iOz) > 2.3-------- (2) However, CaO) is the total amount of Ca in the raw material, and (S
iO□) is the weight% of the total amount of St converted to 5i02 0.4 (Ca) + 1.14 (St) + 1
.. 33 (C) > 9 - (3) However, [Ca] is the total calcium content (weight%) in calcium carbide and calcium silicon, and C3i) is the total silicon content (weight %) in silicon carbide, calcium silicon, and ferrosilicon. %).

〔作 用〕[For production]

本発明の作用を以下に説明する。先づその成分について
説明する。生石灰を50重量%以上含有させることとし
たが、これは脱硫等の反応性がよいスラグを作るためで
ある。又本精錬剤は成形加工された精錬剤であるが、後
述するごと(生石灰が50重量%以下では加圧成形した
成形品の強度が低い。更に本発明では粉粒状の生石灰を
原料とするが、微粒であるために迅速に溶融して均質な
スラグとなり、スラグ中には従来の塊状の生石灰の使用
時にみられた未反応の生石灰粒子はない。
The operation of the present invention will be explained below. First, the ingredients will be explained. It was decided to contain quicklime in an amount of 50% by weight or more in order to create a slag with good reactivity for desulfurization and the like. In addition, although this refining agent is a refining agent that has been molded, as will be described later (if the quicklime content is less than 50% by weight, the strength of the pressure-molded molded product will be low.Furthermore, in the present invention, granular quicklime is used as the raw material). Because it is a fine particle, it melts quickly to form a homogeneous slag, and there are no unreacted quicklime particles in the slag that are found when conventional lump quicklime is used.

螢石を5〜20重量%含有させることとしたが、これは
精錬剤の滓化を促進し反応性を高めるためである。炭化
カルシウムを10重量%以下で含有させることとしたが
、これは炭化カルシウムが強い脱硫、脱燐力を有するた
めである。しかし螢石と同様に、過剰に含有させると耐
火物の損傷が大きくなる。次に脱酸剤の含有量としては
、第3式%式% (C)で規定される脱酸力を9以上とすることとしたが
、これは本精錬剤1 kg中には、9/100kg以上
の溶鋼中の酸素の除去に必要な当量の脱酸剤を含有さ、
せたもので、適当量(通常は溶鋼1トン当たり数kg)
の添加により溶鋼を十分に脱酸するためである。本精錬
剤に含まれる炭素の合計量は第1式に示した如く、(C
)<6以下としたが、これは本精錬剤を上記の適当量使
用した際に、溶鋼の炭素含有量の上昇を支障のない範囲
とするためである。更に本精錬剤では、第2式に示した
如<  (Cab)/ (S i 02 )>2.3と
したが、これは反応性の優れたスラグを成形させるため
である。
It was decided to contain 5 to 20% by weight of fluorite in order to promote slag formation of the refining agent and increase reactivity. It was decided to contain calcium carbide in an amount of 10% by weight or less because calcium carbide has strong desulfurization and dephosphorization power. However, like fluorite, if it is included in excess, it will cause greater damage to refractories. Next, as for the content of the deoxidizing agent, it was decided that the deoxidizing power specified by the third formula % formula % (C) should be 9 or more. Contains the equivalent amount of deoxidizing agent required to remove oxygen from 100 kg or more of molten steel,
suitable amount (usually several kg per ton of molten steel)
This is to sufficiently deoxidize the molten steel by adding . The total amount of carbon contained in this refining agent is (C
)<6 or less, in order to keep the carbon content of molten steel within a range that does not cause any problem when the above-mentioned appropriate amount of the present refining agent is used. Furthermore, in this refining agent, < (Cab)/(S i 02 )> was set to 2.3 as shown in the second equation, in order to form a slag with excellent reactivity.

次に本精錬剤を、各成分の粉粒物を均一に混合したあと
成形品とした理由を説明する。第1表は精錬剤が粒又は
塊の単なる混合物の場合と、本発明のごとく全ての成分
を粉粒物とし均一に混合したあと成形品とした場合につ
いて、両精錬剤の溶融性及び反応性を比較し示したもの
である。成分はどちらもCaO:65重量%、CaF2
 :20重量%、Ca Ct  : 5重量%、SiC
:5重量%、フェロシリコン:5重量%であり、成形品
は各成分を5鶴以下に粉砕し、均一に混合し、10〜2
0flの球状に加圧成形した成形品であり、混合物とは
各成分の粒度が10〜20mmである単なる混合物であ
る。溶融性や反応性の比較試験は、珪化モリブデン抵抗
光熱炉を用い、高炉銑1500ダラムを1630℃に溶
融加熱し、溶融した高炉銑の上に成形品又は混合物を3
0グラム添加した。
Next, the reason why this refining agent is made into a molded product after uniformly mixing the powders and granules of each component will be explained. Table 1 shows the melting properties and reactivity of both refining agents, when the refining agent is a simple mixture of grains or lumps, and when the refining agent is a mixture of particles or lumps, and when all the components are uniformly mixed as powder and granules as in the present invention. This is a comparison. Ingredients for both are CaO: 65% by weight, CaF2
: 20% by weight, Ca Ct: 5% by weight, SiC
: 5% by weight, ferrosilicon: 5% by weight, and the molded product is made by pulverizing each component to 5% by weight or less, mixing uniformly, and 10 to 2% by weight.
It is a molded article pressure-molded into a spherical shape of 0 fl, and the mixture is simply a mixture in which each component has a particle size of 10 to 20 mm. Comparative tests of meltability and reactivity were conducted using a molybdenum silicide resistance photothermal furnace, melting and heating 1500 duram of blast furnace pig to 1630℃, and placing 3 molded products or mixtures on top of the molten blast furnace pig.
0 grams added.

成形品、混合物の何れの場合も、添加後は炉内に7分間
静置し、その後溶銑とスラグを攪拌し脱硫性を調査した
After addition, both the molded product and the mixture were allowed to stand in the furnace for 7 minutes, and then the hot metal and slag were stirred to investigate desulfurization properties.

第  1  表 第1表から明らかな如く、従来の添加物は溶融に時間が
かかりまた脱硫率も低く、従って本発明が目的としてい
る、受鋼槽に予め入れ置き受鋼時の溶鋼の強力な攪拌力
により、短時間に脱酸、造滓および脱硫を行うための添
加剤としては不満足であるが、粉砕した各成分を混合し
成形した本精錬剤は溶融が早く、且反応性にも富み、従
って受鋼に際しての短時間の溶鋼の撹拌力によって、脱
酸、造滓および脱硫が可能な精錬剤である。次に精錬剤
の成形方法について説明する。本発明で粉粒物とはサイ
ズが5 mm以下好ましくはl u+以下をいう、粉粒
物のサイズがこれより大きいと加圧成形が困難となる。
Table 1 As is clear from Table 1, conventional additives take a long time to melt and have a low desulfurization rate. Although it is unsatisfactory as an additive for deoxidizing, slag-forming, and desulfurization in a short time due to stirring power, this refining agent, which is made by mixing and molding each crushed component, melts quickly and is highly reactive. Therefore, it is a refining agent that can deoxidize, create slag, and desulfurize by stirring the molten steel for a short time during steel receiving. Next, a method for molding the refining agent will be explained. In the present invention, the term "powder and granule" refers to a size of 5 mm or less, preferably LU+ or less; if the size of the powder or granule is larger than this, pressure molding becomes difficult.

又生石灰の割合が50%よりも低いと成形品の強度が低
く、輸送や取扱いに際し粉を発生し易い。第2表は加圧
成形の例であるが、CaF、:2重量部、CuCz:1
重足部、SiC:1重置部、及びフェロシリコンゴ1重
附部の粉粒物を混合し、これにCaOの粉粒物を第2表
の割合で混じ、21′+−ル式のブリゲット成形機で1
70 kg / crlのロール圧力で、30關×20
mmXIQ+amのアーモンド型のブリゲットを成形し
た。
If the proportion of quicklime is lower than 50%, the strength of the molded product will be low and powder will easily be generated during transportation and handling. Table 2 is an example of pressure molding, CaF: 2 parts by weight, CuCz: 1
The powder and granules of the heavy foot part, SiC: 1 overlap part, and ferrosilicon Go 1 overlap part were mixed, and the powder and granule of CaO was mixed with this in the proportions shown in Table 2, and the mixture was heated using the 21' + - rule method. 1 with Brigette molding machine
30mm x 20 with roll pressure of 70kg/crl
An almond-shaped brigette of mmXIQ+am was molded.

第2表 第2表にみられる如く、CaOの混合割合が60%の場
合は圧潰強度は充分に太きく15kg以上であり、この
場合は成形物を約2mの高さから鉄床上え落下させても
、殆んど粉は発生しない状態となる。成形方法としては
加圧成形以外に、バインダーを用い造粒成形することも
できるが、バインダーとしてはピッチ、アスファルト、
パラフィン、ワックス、粘土、澱粉、ラテックス等が挙
げられる。本発明の精錬剤は既に述べた如く、従来の添
加物よりも溶融性、反応性がよいが、精錬剤をより短時
間で溶融、反応させたい場合は、熱崩壊剤の粉粒物を5
重量%以下の量を混じて成形するのがよい。熱崩壊剤と
しては、蛭石、真珠岩、黒曜石、松脂石、膨張頁岩等が
適当である。熱崩壊剤は700°〜1500℃で体積膨
張が大きく、従って精錬剤は、受鋼流に捲き込まれた時
に粉状となるため迅速に溶融されて反応性もよくなる。
Table 2 As shown in Table 2, when the CaO mixing ratio is 60%, the crushing strength is sufficiently large and is 15 kg or more, and in this case, the molded product is dropped from an anvil from a height of about 2 m. However, almost no powder is generated. In addition to pressure molding, granulation molding using a binder can also be used as a molding method, but pitch, asphalt,
Examples include paraffin, wax, clay, starch, latex, etc. As mentioned above, the refining agent of the present invention has better meltability and reactivity than conventional additives, but if you want to melt and react the refining agent in a shorter time, add 50% of the heat disintegrating agent powder.
It is preferable to mix and mold in an amount of less than % by weight. Suitable thermal disintegrants include vermiculite, perlite, obsidian, pinestone, and expanded shale. The thermal disintegrant has a large volumetric expansion at 700° to 1500°C, and therefore, the refining agent becomes powder when it is drawn into the receiving steel stream, so it is rapidly melted and has good reactivity.

本発明の精錬剤は、前記以外の構成原料については特に
限定はしないが、酸化アルミニウムや川砂等も溶融性や
反応性をよくするために望ましい構成原料である。
The refining agent of the present invention does not particularly limit the constituent raw materials other than those mentioned above, but aluminum oxide, river sand, and the like are also desirable constituent raw materials in order to improve meltability and reactivity.

〔実施例〕〔Example〕

1、ボトムタッピング方式の電気炉における出鋼中の溶
鋼の攪拌エネルギーを利用し、予め本精錬剤を受綱用取
鍋精錬炉に入れ置し、溶解、滓化の促進を図ったが、そ
の実施例を下記に示した。
1. Using the energy of stirring molten steel during tapping in a bottom-tapping type electric furnace, this refining agent was placed in advance in a ladle refining furnace for receiving wire to promote melting and slag formation. Examples are shown below.

イ、使用電気炉:ボトムタップ式120トン電気炉口、
二次精錬工程=120トン取鍋精錬炉ハ、精錬剤入れ置
量:500kg/lチャージニ、滓化時間の短縮:従来
約15分を5分としたホ、使用電力量の減少:約20%
の減少へ、脱硫率の向上:約25%の向上 以上の如(、二次精錬工程での滓化時間を短縮し、使用
電力を減少できた。また脱硫等の二次精錬が容易となっ
た。これはボトムタップシステムによる電気炉酸化滓を
二次精錬工程へ持ち込まないことの複合メリットの例で
ある。
B. Electric furnace used: Bottom tap type 120 ton electric furnace mouth,
Secondary refining process = 120 tons ladle smelting furnace C, Refining agent amount: 500 kg/l charge, Shortened slaging time: 5 minutes instead of about 15 minutes E, Reduction in power consumption: Approximately 20%
The desulfurization rate improved by about 25% or more (the slag time in the secondary smelting process was shortened and the power consumption was reduced. Also, secondary smelting such as desulfurization became easier). This is an example of the combined benefits of a bottom tap system that prevents electric furnace oxide slag from being carried into the secondary refining process.

2、ボトムタップ方式の電気炉において、電気炉酸化滓
を二次精錬工程へ持ちこまない操業が可能となったが、
その二次精錬工程で本発明の精錬4剤を使用した実施例
を下記に示した。
2. With bottom-tap type electric furnaces, it is now possible to operate the electric furnace without bringing oxidized slag into the secondary refining process.
Examples in which the four refining agents of the present invention were used in the secondary refining step are shown below.

イ、使用電気炉:ボトムタップ弐120トン電気炉口、
二次精錬工程:120)ン取鍋精錬炉ハ、精錬剤入れ置
量:1000kg/lチャージニ、滓化時間の短縮:従
来の15分を11分としたホ、使用電力量の減少:約1
0%の減少へ、脱硫率の向上:約10%の向上 以上の如く、二次精錬工程での滓化時間を短縮し使用電
力を減少できた。又脱硫等の二次精錬が容易になった。
B. Electric furnace used: bottom tap 2 120 ton electric furnace mouth,
Secondary refining process: 120) Ladle smelting furnace C, Refining agent amount: 1000 kg/l charge, Reduction of slag time: 11 minutes instead of 15 minutes E, Reduction in power consumption: Approximately 1
0% reduction in desulfurization rate: As shown by the approximately 10% improvement, it was possible to shorten the slag formation time in the secondary refining process and reduce power consumption. Also, secondary refining such as desulfurization has become easier.

〔効 果〕〔effect〕

本精錬剤を炉外精錬に使用した場合を主に説明したが、
本精錬剤は溶融性、反応性がよいために、炉内還元時に
使用しても効果が大きい。即ち製鋼工程での酸化期終了
後の溶鋼に対する還元炉内及び炉外精錬に於て、本精錬
剤を使用することで、従来技術の説明で列挙した問題点
を一挙に解決した。
Although we mainly explained the case where this refining agent is used for out-of-furnace refining,
This refining agent has good melting properties and reactivity, so it is highly effective when used during in-furnace reduction. That is, by using the present refining agent in the refining of molten steel after the oxidation period in the steelmaking process, both inside and outside the reduction furnace, the problems listed in the description of the prior art were solved at once.

高級化指向に基づく分割精錬技術が進歩して、従来の溶
解、酸化精錬、還元精錬の三つの機能が分れ還元精錬が
炉外設備で行われるようになってきたが、この場合前工
程のスラグを次工程に持込ないことが必要で、又滓化の
早い複合添加物が必要となったが、本発明はこの要望を
満すものである。精錬方式自体は分割により、シンプル
になった反面、精錬剤に関してはハンドリング合理化の
ための単一化や、精錬能が高く電力ロスの少ないものが
望まれるが、本発明はワンタッチ式精錬剤でありその要
望を満すものである。
With the advancement of split refining technology based on the trend toward higher-grade products, the conventional three functions of melting, oxidation refining, and reduction refining have been separated, and reduction refining has come to be performed in equipment outside the furnace. It is necessary not to carry slag into the next process, and a composite additive that quickly turns into slag has become necessary, and the present invention satisfies this need. Although the refining method itself has become simpler through division, it is desired that the refining agent be unified to streamline handling, and that it has high refining performance and less power loss.However, the present invention is a one-touch refining agent. It satisfies that demand.

精錬剤としては、出鋼流中に投入し又は取鍋中に入れ置
し、その上から溶鋼を受鋼してその攪拌エネルギーを利
用することにより反応の促進をはかり、二次精錬の負荷
を軽減するものが望ましいが、本発明はこのような使用
方法に適した精錬剤である。
As a refining agent, it can be thrown into the tapping stream or placed in a ladle to receive molten steel from above and use the stirring energy to accelerate the reaction and reduce the load on secondary refining. The present invention is a refining agent suitable for such a method of use.

従来の添加物は、粉塵等作業環境上からも出鋼という限
られた時間内の投入が出来ないために、出鋼後に投入し
電気エネルギーにより滓化を行っていたが、本発明によ
り粉塵の発生はなく、又滓化のための通電が不必要とな
った。
Conventional additives could not be added during the limited time of tapping due to dust and other work environment issues, so they were added after tapping and turned into slag using electrical energy.However, the present invention eliminates dust. There was no occurrence, and there was no need to apply electricity for slag formation.

特許!!I願人  トピーエ業株式会社矢橋工業株式会
Patent! ! I Applicant Topie Industry Co., Ltd. Yabashi Kogyo Co., Ltd.

Claims (1)

【特許請求の範囲】 1、生石灰が50重量%以上、螢石が5−20重量%、
炭化カルシウムが10重量%以下でかつ下記の第(1)
〜(3)式で規定される量の脱酸剤及び炭素を含有する
混合物であって、各成分を粉粒物とし、均一に混合した
あと加圧成型しあるいはバインダーを用いて造粒成型し
た複合精錬剤。 〔C〕<6……………………………(1) 但し〔C〕は原料の炭素量の合計(重量%)(CaO)
/(SiO_2)>2.3………(2)但し(CaO)
は原料のCaの全量をCaOに、又(SiO_2)はS
iの全量をSiO_2に換算した重量% 0.4〔Ca〕+1.14〔Si〕+1.33〔C〕>
9……(3)但し〔Ca〕は炭化カルシウム、カルシウ
ムシリコン中のカルシウム分の合計(重量%)、〔Si
〕は炭化珪素、カルシウムシリコン、フェロシリコン中
の珪素分の合計(重量%)である。 2、生石灰が50重量%以上、螢石が5〜20重量%、
炭化カルシウムが10重量%以下で、かつ所定量の脱酸
剤及び炭素を含有する原料に、熱崩壊剤として、蛭石、
真珠岩、黒曜石、松脂石、膨張頁岩の一種若しくは2種
以上を5重量%以下の量加えた混合物であって、各成分
を粉粒物とし、均一に混合したあと加圧成形しあるいは
バインダーを用いて造粒成形した熱崩壊型複合精錬剤。 3、生石灰が50重量%以上、螢石が5〜20重量%、
炭化カルシウムが10重量%以下でかつ所定量の脱酸剤
及び炭素を含有する複合精錬剤あるいは熱崩壊型複合精
錬剤を、受鋼槽内に予め入れ置し、スラグを分離した溶
鋼を受鋼し、受鋼時の溶鋼流の強力な攪拌力により、短
時間で脱酸、造滓および脱流を行うことを特徴とする溶
鋼の精錬方法。
[Claims] 1. Quicklime is 50% by weight or more, fluorite is 5-20% by weight,
Calcium carbide is 10% by weight or less and the following item (1)
~A mixture containing an amount of a deoxidizing agent and carbon specified by formula (3), in which each component is made into powder and granules, mixed uniformly, and then pressure molded or granulated using a binder. Composite refining agent. [C]<6………………………………(1) However, [C] is the total amount of carbon in the raw materials (weight%) (CaO)
/(SiO_2)>2.3……(2) However (CaO)
(SiO_2) is S
Weight% of total amount of i converted to SiO_2 0.4 [Ca] + 1.14 [Si] + 1.33 [C]>
9...(3) However, [Ca] is the total calcium content (weight%) in calcium carbide and calcium silicon, [Si
] is the total silicon content (% by weight) in silicon carbide, calcium silicon, and ferrosilicon. 2. Quicklime is 50% by weight or more, fluorite is 5-20% by weight,
A raw material containing 10% by weight or less of calcium carbide and a predetermined amount of deoxidizing agent and carbon, as a heat disintegrating agent, vermiculite,
A mixture containing one or more of pearlite, obsidian, pinestone, and expanded shale in an amount of 5% by weight or less, each component being made into powder and granules, mixed uniformly, and then pressure molded or a binder is added. A heat-decomposable composite refining agent granulated using 3. Quicklime is 50% by weight or more, fluorite is 5-20% by weight,
A composite refining agent or heat-decomposable composite refining agent containing 10% by weight or less of calcium carbide and a predetermined amount of deoxidizing agent and carbon is placed in a steel receiving tank in advance, and the molten steel from which the slag has been separated is received. A molten steel refining method characterized by deoxidizing, slag forming, and deflowing in a short time using the strong stirring force of the molten steel flow during receiving.
JP61000262A 1986-01-07 1986-01-07 Composite refining agent and refining method Granted JPS62158814A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP61000262A JPS62158814A (en) 1986-01-07 1986-01-07 Composite refining agent and refining method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61000262A JPS62158814A (en) 1986-01-07 1986-01-07 Composite refining agent and refining method

Publications (2)

Publication Number Publication Date
JPS62158814A true JPS62158814A (en) 1987-07-14
JPH0364566B2 JPH0364566B2 (en) 1991-10-07

Family

ID=11468996

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61000262A Granted JPS62158814A (en) 1986-01-07 1986-01-07 Composite refining agent and refining method

Country Status (1)

Country Link
JP (1) JPS62158814A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003155516A (en) * 2001-11-15 2003-05-30 Kawasaki Steel Corp Method for desulfurizing molten steel with ladle- refining
CN113502372A (en) * 2021-05-26 2021-10-15 山东鲁丽钢铁有限公司 Rapid white slag making material for 120tLF refining furnace and process

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS51109208A (en) * 1975-03-24 1976-09-28 Komatsu Mfg Co Ltd

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS51109208A (en) * 1975-03-24 1976-09-28 Komatsu Mfg Co Ltd

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003155516A (en) * 2001-11-15 2003-05-30 Kawasaki Steel Corp Method for desulfurizing molten steel with ladle- refining
CN113502372A (en) * 2021-05-26 2021-10-15 山东鲁丽钢铁有限公司 Rapid white slag making material for 120tLF refining furnace and process

Also Published As

Publication number Publication date
JPH0364566B2 (en) 1991-10-07

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