JPH04308016A - Method for preventing pressure foaming - Google Patents
Method for preventing pressure foamingInfo
- Publication number
- JPH04308016A JPH04308016A JP9801091A JP9801091A JPH04308016A JP H04308016 A JPH04308016 A JP H04308016A JP 9801091 A JP9801091 A JP 9801091A JP 9801091 A JP9801091 A JP 9801091A JP H04308016 A JPH04308016 A JP H04308016A
- Authority
- JP
- Japan
- Prior art keywords
- slag
- refining
- vessel
- hot metal
- foaming
- 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
Links
- 238000005187 foaming Methods 0.000 title claims abstract description 30
- 238000000034 method Methods 0.000 title claims description 34
- 239000002893 slag Substances 0.000 claims abstract description 58
- 238000007670 refining Methods 0.000 claims abstract description 35
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 18
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 17
- 238000007664 blowing Methods 0.000 claims abstract description 10
- 238000002203 pretreatment Methods 0.000 claims abstract description 5
- 239000002184 metal Substances 0.000 claims description 32
- 229910052751 metal Inorganic materials 0.000 claims description 32
- 235000008733 Citrus aurantifolia Nutrition 0.000 claims description 9
- 235000011941 Tilia x europaea Nutrition 0.000 claims description 9
- 239000004571 lime Substances 0.000 claims description 9
- 239000002245 particle Substances 0.000 claims description 6
- 238000003723 Smelting Methods 0.000 claims 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract description 24
- 229910052742 iron Inorganic materials 0.000 abstract description 12
- 238000006477 desulfuration reaction Methods 0.000 abstract description 11
- 230000023556 desulfurization Effects 0.000 abstract description 11
- 229910000831 Steel Inorganic materials 0.000 abstract description 4
- 239000010959 steel Substances 0.000 abstract description 4
- 239000003245 coal Substances 0.000 abstract description 2
- 239000000843 powder Substances 0.000 description 10
- 238000011282 treatment Methods 0.000 description 10
- 230000005587 bubbling Effects 0.000 description 7
- 238000002347 injection Methods 0.000 description 6
- 239000007924 injection Substances 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 4
- 239000000571 coke Substances 0.000 description 4
- 239000007789 gas Substances 0.000 description 4
- 229910052698 phosphorus Inorganic materials 0.000 description 4
- 239000011574 phosphorus Substances 0.000 description 4
- 229910052717 sulfur Inorganic materials 0.000 description 4
- 239000011593 sulfur Substances 0.000 description 4
- 238000010586 diagram Methods 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 238000005266 casting Methods 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000009749 continuous casting Methods 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 229910001873 dinitrogen Inorganic materials 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 238000009628 steelmaking Methods 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 230000009172 bursting Effects 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 230000001914 calming effect Effects 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000012159 carrier gas Substances 0.000 description 1
- 238000004581 coalescence Methods 0.000 description 1
- 229910052681 coesite Inorganic materials 0.000 description 1
- 229910052906 cristobalite Inorganic materials 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 229910001882 dioxygen Inorganic materials 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 238000009991 scouring Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 229910052682 stishovite Inorganic materials 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910052905 tridymite Inorganic materials 0.000 description 1
Landscapes
- Refinement Of Pig-Iron, Manufacture Of Cast Iron, And Steel Manufacture Other Than In Revolving Furnaces (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は溶鉄を転炉にて脱炭して
鋼を精錬する工程において、溶鉄を転炉に挿入する前に
石灰、スケールその他の精錬剤を添加して溶銑の脱燐脱
硫を行なう溶銑予備処理法に関するものである。[Industrial Application Field] The present invention is used in the process of decarburizing molten iron in a converter to refine steel. This invention relates to a hot metal pretreatment method for phosphorus desulfurization.
【0002】0002
【従来の技術】溶鉄を転炉にて高圧酸素の吹き付けまた
は吹き込みにより脱炭して鋼を精錬する場合、転炉では
脱炭するだけでなく鋼の目標成分に応じて脱燐脱硫を行
なうために、通常石灰その他の精錬剤を添加することが
必要である。この場合転炉吹錬初期の脱珪素反応により
生成するSiO2を主成分とするスラグを高塩基度のス
ラグに変える為に大量の石灰を投入する必要が生じる。
近年、この石灰使用量を削減して経済的に脱燐脱硫処理
を行なうために、溶鉄を予め別の容器で脱燐脱硫処理す
るいわゆる溶銑予備処理法が広く一般に行なわれている
。この場合溶銑予備処理用の容器には溶銑の搬送容器で
あるトピードカーや溶銑鍋が使用され、これらの容器は
本来精錬用の容器ではないためにフリーボードが小さく
、脱燐脱硫処理中にスラグが泡立ち、スラグ流出を生じ
ることが多い。このようなスラグ流出に対する対策とし
て従来2つの方法がとられていた。その第1はスラグ流
出が始まるまで一時精錬剤の吹き込みを中断する方法で
ある。もう一つの方法はスラグが流出しても精錬処理後
にピット内の流出スラグを搬出する方法である。これら
の方法には以下の問題点がある。まず精錬剤の吹き込み
を中断する第一の方法の場合、処理の中断は処理時間の
延長をもたらし、転炉から連続鋳造にいたる一連の円滑
な物流が阻害され、ひいては生産性の悪化をもたらす。
また流出スラグ用のピットを配置する方法の場合、流出
スラグ中には通常10%程度の鉄分が含まれているので
、鉄歩留まりが悪化するという問題があるだけでなく、
ピットを配置するための設備費やピット内スラグを搬出
する等の新たな作業が必要となり経済的ではない。
これらの問題点によってきたる根本原因は、脱燐中には
溶銑とスラグの界面近傍において、添加したスケールや
酸素ガスと溶鉄中の炭素との反応によりCOガスが発生
し、このCO気泡によりスラグが泡立ち、スラグの体積
が4〜8倍程度に膨張することによる。しかしながらこ
れらの泡立ちを経済的に防止する方法がなかったために
止むなく上記対策を講じ、それによって上記問題点が生
じたものである。[Prior Art] When refining steel by decarburizing molten iron by blowing or blowing high-pressure oxygen in a converter, the converter not only decarburizes it, but also dephosphorizes and desulphurizes it according to the target composition of the steel. It is usually necessary to add lime or other scouring agents. In this case, it is necessary to add a large amount of lime to convert the slag mainly composed of SiO2 produced by the desiliconization reaction in the early stage of converter blowing into slag with high basicity. In recent years, in order to economically perform dephosphorization and desulfurization by reducing the amount of lime used, a so-called hot metal pretreatment method in which molten iron is previously subjected to dephosphorization and desulfurization in a separate container has been widely used. In this case, a torpedo car or hot metal pot, which is a container for transporting hot metal, is used as a container for hot metal pretreatment, and since these containers are not originally used for refining, the freeboard is small, and slag is generated during the dephosphorization and desulfurization treatment. Often causes foaming and slag outflow. Conventionally, two methods have been taken as countermeasures against such slag outflow. The first method is to temporarily suspend the injection of the refining agent until the slag begins to flow out. Another method is to transport the slag out of the pit after the refining process even if the slag flows out. These methods have the following problems. In the case of the first method, which involves interrupting the injection of refining agents, interrupting the process results in an extension of the process time, impeding the series of smooth physical distribution from the converter to continuous casting, and ultimately leading to a deterioration in productivity. In addition, in the case of the method of arranging pits for spilled slag, since the spilled slag usually contains about 10% iron, there is a problem that not only the iron yield deteriorates, but also
This is not economical because it requires equipment costs for arranging the pit and new work such as carrying out the slag in the pit. The root cause of these problems is that during dephosphorization, CO gas is generated near the interface between hot metal and slag due to the reaction between added scale and oxygen gas and carbon in the molten iron, and these CO bubbles cause slag to grow. This is caused by foaming and the volume of the slag expanding by about 4 to 8 times. However, since there was no way to economically prevent these bubbling, the above-mentioned measures had to be taken, which caused the above-mentioned problems.
【0003】0003
【発明が解決しようとする課題】本発明は以上の事情に
鑑みてなされたもので、従来の問題点の根本原因である
スラグの泡立ちを効果的に抑制してスラグ流出を防止し
、経済的に溶銑予備処理を行なう方法を提供することを
目的としたものである。[Problems to be Solved by the Invention] The present invention has been made in view of the above circumstances, and it is an object of the present invention to effectively suppress slag bubbling, which is the root cause of the conventional problems, to prevent slag outflow, and to achieve an economical The purpose of this invention is to provide a method for pre-treating hot metal.
【0004】0004
【課題を解決するための手段】本発明はスラグの泡立ち
が、脱燐処理中に発生したCOガス気泡によりスラグの
体積が膨張することによって生じ、その泡立ち高さは主
に気泡と気泡の間のスラグ液膜の安定性および雰囲気圧
力によって支配され、雰囲気圧力が高いほど泡立ち高さ
が小さいことや、スラグと濡れにくい物質である炭剤を
添加し気泡間のスラグ液膜を破壊して気泡の合体や気泡
の破裂を促進することにより泡立ち高さが低下すること
、および脱燐処理中の泡立ち高さは補助ランスに設置し
た振動計の振動強度によって泡立ち高さが推定できるこ
と等の本発明者らの新知見に基づきなされたものであり
、その要旨とするところは、精錬容器内を密閉式とし、
かつ精錬剤吹き込み用ランスとは異なる精錬容器内補助
ランスに振動計を設置して振動強度を連続的に測定し、
スラグ泡立ち高さが容器高さの範囲内に維持されるよう
に振動強度の増加に応じて容器内の圧力を制御し、精錬
終了後に粒径3mm以下のコークス粉を溶銑トン当り0
.1kg以上添加した後容器内圧力を常圧に復圧するこ
とを特徴とするスラグフォーミング防止法である。[Means for Solving the Problems] The present invention provides that the foaming of slag is caused by the expansion of the volume of the slag due to the CO gas bubbles generated during dephosphorization treatment, and the height of the foaming is mainly determined between the bubbles. It is controlled by the stability of the slag liquid film and the atmospheric pressure, and the higher the atmospheric pressure, the smaller the foaming height, and the addition of carbonaceous agent, which is a substance that is difficult to wet with the slag, destroys the slag liquid film between the bubbles and creates bubbles. According to the present invention, the foaming height is reduced by promoting coalescence and bursting of bubbles, and the foaming height during dephosphorization treatment can be estimated by the vibration intensity of a vibration meter installed in the auxiliary lance. This was done based on the new knowledge of the researchers, and its gist is that the inside of the refining vessel should be sealed,
In addition, a vibration meter was installed in the auxiliary lance inside the refining vessel, which is different from the lance for blowing the refining agent, and the vibration intensity was continuously measured.
The pressure inside the container is controlled according to the increase in vibration intensity so that the slag bubbling height is maintained within the range of the container height, and after the completion of refining, coke powder with a particle size of 3 mm or less is produced per ton of hot metal.
.. This method of preventing slag foaming is characterized by restoring the pressure inside the container to normal pressure after adding 1 kg or more.
【0005】以下に本発明を更に詳細に説明する。まず
この発明が適用される工程について説明する。本発明が
適用される工程は溶銑に石灰、スケールその他の精錬剤
を添加して溶銑の脱燐脱硫を行なう溶銑予備処理工程で
ある。溶銑予備処理を行なう精錬容器としては通常トピ
ードカーもしくは溶銑鍋が適用されるが、容器外へのス
ラグ流出や泡立ち高さが問題となる場合には転炉などそ
の他の容器であってもさしつかえない。また精錬剤とし
ては通常石灰およびスケールが用いられるが、炭酸ソー
ダ等その他の精錬剤であっても本発明が適用できること
はいうまでもない。また溶銑予備処理時のスラグ流出が
特に問題となるのは脱燐脱硫を目的とした精錬工程であ
るが、脱燐前の脱珪処理等、その他の目的の精錬処理で
あっても、スラグ流出や泡立ち高さが問題となる限り、
本発明の適用は有効である。すなわち本発明は精錬用ス
ラグの泡立ち高さの制御が必要な溶銑予備処理工程であ
ればいかなる工程であっても適用できるものである。The present invention will be explained in more detail below. First, a process to which this invention is applied will be explained. The process to which the present invention is applied is a hot metal pretreatment process in which lime, scale, and other refining agents are added to the hot metal to perform dephosphorization and desulfurization of the hot metal. A torpedo car or a hot metal ladle is usually used as the refining vessel for hot metal pretreatment, but if slag leakage outside the vessel or high foaming is a problem, other vessels such as a converter may also be used. Although lime and scale are usually used as refining agents, it goes without saying that the present invention is also applicable to other refining agents such as soda carbonate. In addition, slag outflow during hot metal pretreatment is a particular problem in the refining process for the purpose of dephosphorization and desulfurization, but even in refining processes for other purposes, such as desiliconization treatment before dephosphorization, slag outflow is a problem. As long as foaming height is a problem,
Application of the present invention is effective. That is, the present invention can be applied to any hot metal pretreatment process that requires control of the foaming height of refining slag.
【0006】本発明を適用する上で最も重要な作業は、
精錬容器内を密閉式とし、かつ精錬剤吹き込み用ランス
とは異なる精錬容器内補助ランスに振動計を設置して振
動強度を連続的に測定し、スラグ泡立ち高さが容器高さ
の範囲内に維持されるように振動強度の増加に応じて容
器内の圧力を制御し、精錬終了後に粒径3mm以下のコ
ークス粉を溶銑トン当り0.1kg以上添加した後容器
内圧力を常圧に復圧する点にある。まず泡立ち高さの推
定について述べる。泡立ち高さの推定法としては、電気
抵抗法やファイバースコープによる炉内観察法等がある
が、測定の信頼性が乏しく実用的ではない。本発明者ら
は種々実験を重ねた結果、精錬剤吹き込み用ランスとは
異なる補助ランスに振動計を設置して振動強度を測定す
る方法が最も信頼性があることが分かった。振動計を設
置するランスは石灰やスケール等の精錬剤を吹き込むラ
ンスとは別個に設けることが重要である。本発明者らは
精錬剤吹き込み用ランスに振動計を設置した場合には、
スラグ泡立ち高さと振動強度の間に相関関係は見られな
いが、該ランスとは別個に補助ランスを設け、この補助
ランスに振動計を設置した場合には図1に示すようにス
ラグ泡立ち高さと振動強度の間に明瞭な相関関係が認め
られることを見いだした。なおこの補助ランスは精錬用
粉体吹き込み用のランスではないことが重要であり、ガ
スのみの吹き込みであれば支障はなく、例えば気体酸素
吹き込み用のランスであっても良い。The most important task in applying the present invention is
The inside of the refining vessel is sealed, and a vibration meter is installed in the auxiliary lance inside the refining vessel, which is different from the lance for blowing refining agent, to continuously measure the vibration intensity, and the height of slag bubbling is within the range of the height of the vessel. The pressure inside the vessel is controlled according to the increase in vibration intensity so that the pressure is maintained, and after the completion of refining, the pressure inside the vessel is restored to normal pressure after adding 0.1 kg or more of coke powder with a particle size of 3 mm or less per ton of hot metal. At the point. First, we will discuss the estimation of foaming height. Methods for estimating the foaming height include the electrical resistance method and the furnace observation method using a fiberscope, but the measurement reliability is poor and is not practical. As a result of various experiments, the present inventors found that the most reliable method was to install a vibration meter on an auxiliary lance different from the refining agent injection lance and measure the vibration intensity. It is important that the lance where the vibration meter is installed is separate from the lance where the refining agents such as lime and scale are injected. When the present inventors installed a vibration meter on the refining agent injection lance,
There is no correlation between the slag foaming height and the vibration intensity, but if an auxiliary lance is provided separately from the lance and a vibration meter is installed on this auxiliary lance, the slag foaming height and vibration intensity will change as shown in Figure 1. A clear correlation was found between the vibration intensities. It is important that this auxiliary lance is not a lance for blowing refining powder; there is no problem if only gas is blown; for example, it may be a lance for blowing gaseous oxygen.
【0007】本発明において重要な第2の点は、図2に
示すように容器内雰囲気圧力を高めることによってスラ
グ泡立ち高さを低く抑えることができるとの本発明者ら
の知見に基づくものである。 したがって、スラグ泡立
ち高さを振動計によって推定し、その結果に応じて容器
内雰囲気を制御することによってスラグ泡立ち高さが容
器高さの範囲内になるようにすることができる。本発明
者らの知見によればこの時の必要圧力は最大でも4気圧
程度であり、工業的に実現可能な圧力レベルでスラグ泡
立ち高さを制御できるのである。The second important point in the present invention is based on the inventors' knowledge that the height of slag foaming can be suppressed by increasing the atmospheric pressure inside the container, as shown in FIG. be. Therefore, by estimating the slag foaming height using a vibration meter and controlling the atmosphere in the container according to the result, the slag foaming height can be made to be within the range of the container height. According to the findings of the present inventors, the required pressure at this time is about 4 atmospheres at most, and the height of slag bubbling can be controlled at an industrially feasible pressure level.
【0008】本発明において重要な第3の点は精錬作業
終了後ランスを引き上げる際に容器内圧力を常圧に復圧
する必要がありこの際にスラグが泡立ち炉口より流出す
ることを防止する手段に関するものである。本発明者ら
は精錬終了後にコークス粉を適量添加することにより、
常圧に復圧した時の炉口からのスラグ流出を防止できる
こと、そしてこの際の条件は図3に示すように、コーク
ス粉のサイズが粒径3mm以下であることおよびその添
加量は溶銑トン当り0.1kg以上必要であることを見
いだした。添加する泡立ち抑制剤はコークス粉が最も有
効であるが、目的に応じてコークス粉の代わりに石炭を
用いたり、コークス粉に炭酸カルシウム等その他の粉体
を混合したものを用いることもできる。その場合でも添
加する粉体中のC成分の量を溶銑トン当り0.5kg以
上添加することによりコークス粉のみを添加するのと同
様の効果を得ることができる。コークス粉のサイズは大
きすぎると添加量に対して粉体粒子の数が少なくなるの
で泡立ちスラグの鎮静効果が不十分となるため、その上
限を1mmとした。図3に示すようにコークス粉のサイ
ズが3mm以下の場合には溶銑トン当り0.1kgのコ
ークスを添加した後の復圧時点でのスラグ泡立ちによる
スラグ流出の発生率が0であるのに対し、コークス粉の
サイズが3mm超の場合にはコークス粉の添加量を多く
してもかなりの確率でスラグ流出が発生する。一方サイ
ズが細かすぎる場合には、粉体が飛散して粉体のロスを
生じる問題があるが、粉体が確実に泡立ちスラグ中に添
加される条件が確保できるならば、サイズの下限を規定
する必要は特にない。添加方法としては、ランスから窒
素ガス等の搬送ガスによって泡立ちスラグ中へ吹き込む
方法が最もこのましいが、スラグ中に確実に分散させる
ことが可能であればランス以外の方法でも差し支えない
。本発明者らの実験によれば、袋詰めした粉体を単に上
方から投入するだけでは泡立ち抑制効果は不十分であり
、スラグ中に粉体を確実に分散させることが必要である
。またコークス粉の吹き込み位置は炉口から300mm
ないし600mmの位置が最も良好であり、同じ効果を
得るためのコークス粉添加量が最も少なく効果的であっ
た。これは粉体がスラグ中に確実に分散されたためであ
る。以下に実施例に基づいて本発明の効果を記す。The third important point in the present invention is that when the lance is pulled up after the completion of the refining work, it is necessary to restore the pressure inside the container to normal pressure, and at this time there is a means to prevent the slag from bubbling and flowing out from the furnace mouth. It is related to. By adding an appropriate amount of coke powder after the completion of refining, the present inventors
It is possible to prevent slag from flowing out from the furnace mouth when the pressure is restored to normal pressure, and the conditions for this are as shown in Figure 3, the size of the coke powder must be 3 mm or less in particle diameter, and the amount added must be equal to or less than 1 ton of hot metal. It has been found that 0.1 kg or more is required per unit. Coke powder is the most effective foaming suppressant to be added, but depending on the purpose, coal may be used instead of coke powder, or coke powder mixed with other powders such as calcium carbonate may also be used. Even in that case, the same effect as when only coke powder is added can be obtained by adding the C component in the powder in an amount of 0.5 kg or more per ton of hot metal. If the size of the coke powder is too large, the number of powder particles will be small relative to the amount added, and the effect of calming the foaming slag will be insufficient, so the upper limit was set to 1 mm. As shown in Figure 3, when the size of coke powder is 3 mm or less, the incidence of slag outflow due to slag foaming at the time of pressure recovery after adding 0.1 kg of coke per ton of hot metal is 0. If the size of the coke powder exceeds 3 mm, there is a high probability that slag will flow out even if the amount of coke powder added is increased. On the other hand, if the size is too small, there is a problem of powder scattering and powder loss, but if conditions can be ensured for the powder to foam and be added to the slag, the lower limit of the size can be specified. There is no particular need to do so. The most preferable method for adding the material is to blow it into the bubbling slag using a carrier gas such as nitrogen gas from a lance, but other methods may be used as long as it is possible to reliably disperse the material into the slag. According to the experiments conducted by the present inventors, simply charging the bagged powder from above is insufficient to suppress foaming, and it is necessary to reliably disperse the powder in the slag. In addition, the coke powder injection position is 300mm from the furnace mouth.
The position between 600 mm and 600 mm was the best, and the amount of coke powder added to obtain the same effect was the smallest and was effective. This is because the powder was reliably dispersed in the slag. The effects of the present invention will be described below based on Examples.
【0009】[0009]
【実施例】高炉から出銑された溶銑250トンをトピー
ドカーに受け、その際スケールを添加して溶銑中の珪素
含有量を0.35%から0.13%に低下せしめた後ス
ラグを排出し、トピードカー内炉口部から溶銑中にラン
スを挿入して窒素ガスを搬送用ガスとしてホタル石を2
0%混合した石灰とスケールを混合状態でそれぞれ溶銑
トン当り21kgおよび15kg吹き込み脱燐脱硫処理
を行なった。この処理により溶銑中の燐含有量は0.1
3%から0.023%に、硫黄含有量は0.020%か
ら0.007%に低下した、一方予め、精錬剤吹き込み
用とは別個に設置した補助ランスに加速度振動計を設置
し、これにより処理中に振動強度を連続的に測定しその
値を自動記録計に記録した。また同時に振動強度の値を
コンピュ−タ−により処理し、その強度が元の強度の1
.0〜1.5倍の範囲内に維持されるように容器内圧力
を自動制御するように予めシステムを作成し、このシス
テムによって容器内圧力を制御した。システムは設計通
りに作動し、処理開始から約9分後以降、徐々に容器内
圧力が増加して約22分後にピークの1.8気圧に達し
、その後徐々に低下して処理終了時点では1.3気圧で
あった。その後粒径100メッシュ以下の微粉コークス
を一分当り80kgの割合で30秒間吹き込んだ後容器
内を常圧に復圧した。復圧時に炉口からのスラグ流出は
見られず順調に処理を終了した。なお、このコークス添
加量は溶銑トン当り0.18kgに相当する。[Example] 250 tons of hot metal tapped from a blast furnace was received in a torpedo car, and after adding scale to reduce the silicon content in the hot metal from 0.35% to 0.13%, the slag was discharged. , a lance is inserted into the hot metal from the furnace opening in the torpedo car, and 2 fluorites are transported using nitrogen gas as a transport gas.
Dephosphorization and desulfurization treatment was carried out by blowing 21 kg and 15 kg of 0% mixed lime and scale per ton of hot metal, respectively. This treatment reduces the phosphorus content in hot metal to 0.1
The sulfur content was reduced from 3% to 0.023%, and the sulfur content was reduced from 0.020% to 0.007%.On the other hand, an acceleration vibrometer was installed in advance on an auxiliary lance that was installed separately from the one for injecting the refining agent. The vibration intensity was continuously measured during the treatment, and the values were recorded on an automatic recorder. At the same time, the value of the vibration intensity is processed by a computer, and the resulting intensity is 1/1 of the original intensity.
.. A system was previously created to automatically control the pressure inside the container so that it was maintained within a range of 0 to 1.5 times, and the pressure inside the container was controlled by this system. The system operates as designed, and the pressure inside the container gradually increases from about 9 minutes after the start of the process, reaching a peak of 1.8 atm after about 22 minutes, and then gradually decreases to 1 atm at the end of the process. The pressure was .3 atm. Thereafter, finely divided coke having a particle size of 100 mesh or less was blown into the container at a rate of 80 kg per minute for 30 seconds, and then the pressure inside the container was restored to normal pressure. No slag leakage from the furnace mouth was observed during pressure recovery, and the process was completed smoothly. Note that this amount of coke added corresponds to 0.18 kg per ton of hot metal.
【0010】0010
【比較例】実施例1と同様にして脱珪および脱燐脱硫処
理を行なった。脱燐処理中にに炉口部からのスラグ流出
が合計4回生じたので、その都度スラグ流出が始まるま
で石灰およびスケールの吹き込みを中断した結果、この
処理により溶銑中の燐含有量は0.13%から0.02
2%に、硫黄含有量は0.019%から0.006%に
低下し目標通りの燐および硫黄含有量が得られたが、脱
燐脱硫に要した合計の処理時間は45分であった。その
結果転炉への溶銑の運搬が遅れ、転炉にて待ち時間が生
じ鋳造工程である連続鋳造において連々鋳が不可能とな
り、その結果連鋳鋳片の鉄歩留まりが2%低下した。[Comparative Example] Desiliconization, dephosphorization, and desulfurization treatments were carried out in the same manner as in Example 1. During the dephosphorization process, slag flowed out from the furnace mouth a total of four times, so the injection of lime and scale was interrupted each time until the slag flow started, and as a result of this process, the phosphorus content in the hot metal was reduced to 0. 13% to 0.02
The sulfur content decreased from 0.019% to 0.006%, achieving the target phosphorus and sulfur content, but the total processing time required for dephosphorization and desulfurization was 45 minutes. . As a result, the transportation of hot metal to the converter was delayed, resulting in waiting time in the converter, making continuous casting impossible in the casting process, and as a result, the iron yield of continuously cast slabs decreased by 2%.
【0011】[0011]
【発明の効果】上述の実施例および比較例から本発明の
方法によれば溶銑予備処理における脱燐脱硫処理を効果
的に行なうことができ、その結果鋳造工程まで含めた全
製鋼工程の物流が円滑になるだけでなく、全製鋼工程に
おける鉄歩留まりの増加をもたらす経済的な方法である
ことが明らかである。[Effects of the Invention] As can be seen from the above-mentioned Examples and Comparative Examples, according to the method of the present invention, dephosphorization and desulfurization treatment in hot metal pretreatment can be carried out effectively, and as a result, the logistics of the entire steelmaking process including the casting process can be improved. It is clear that it is an economical method that not only facilitates but also increases the iron yield in the entire steelmaking process.
【図1】振動強度とスラグ泡立ち高さの関係を示す図、
[Figure 1] Diagram showing the relationship between vibration intensity and slag foaming height,
【図2】スラグ泡立ち高さと容器内圧力の関係を示す図
、[Figure 2] Diagram showing the relationship between slag foaming height and container pressure,
【図3】処理終了に伴う復圧時点でのスラグ流出に及ぼ
すコークス添加量およびコークス粉サイズの影響を示す
図である。FIG. 3 is a diagram showing the influence of the amount of coke added and the size of coke powder on the slag outflow at the time of pressure restoration upon completion of treatment.
Claims (1)
を添加して溶銑の脱珪もしくは脱燐脱硫を行なう溶銑予
備処理法において、精錬容器内を密閉式とし、かつ精錬
剤吹き込み用ランスとは異なる精錬容器内補助ランスに
振動計を設置して振動強度を精錬処理中に連続的に測定
し、スラグ泡立ち高さが容器高さの範囲内に維持される
ように振動強度の増加に応じて容器内の圧力を制御し、
精錬終了後に粒径3mm以下のコークス粉を溶銑トン当
り0.1kg以上添加した後容器内圧力を常圧に復圧す
ることを特徴とするスラグフォーミング防止法。Claim 1: In a hot metal pretreatment method in which lime, scale, and other refining agents are added to hot metal to desiliconize or dephosphorize and desulfurize the hot metal, the inside of the refining vessel is closed, and a lance for blowing the refining agent is used. Vibration meters were installed in the auxiliary lances in different smelting vessels to continuously measure the vibration intensity during the smelting process, and the slag foaming height was maintained within the range of the vessel height according to the increase in vibration intensity. Controls the pressure inside the container,
A method for preventing slag foaming, which comprises adding coke powder with a particle size of 3 mm or less in an amount of 0.1 kg or more per ton of hot metal after completion of refining, and then restoring the pressure inside the vessel to normal pressure.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9801091A JPH0816242B2 (en) | 1991-04-04 | 1991-04-04 | Pressure forming prevention method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9801091A JPH0816242B2 (en) | 1991-04-04 | 1991-04-04 | Pressure forming prevention method |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH04308016A true JPH04308016A (en) | 1992-10-30 |
JPH0816242B2 JPH0816242B2 (en) | 1996-02-21 |
Family
ID=14207790
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP9801091A Expired - Lifetime JPH0816242B2 (en) | 1991-04-04 | 1991-04-04 | Pressure forming prevention method |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0816242B2 (en) |
-
1991
- 1991-04-04 JP JP9801091A patent/JPH0816242B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPH0816242B2 (en) | 1996-02-21 |
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