JPS649373B2 - - Google Patents
Info
- Publication number
- JPS649373B2 JPS649373B2 JP16227383A JP16227383A JPS649373B2 JP S649373 B2 JPS649373 B2 JP S649373B2 JP 16227383 A JP16227383 A JP 16227383A JP 16227383 A JP16227383 A JP 16227383A JP S649373 B2 JPS649373 B2 JP S649373B2
- Authority
- JP
- Japan
- Prior art keywords
- coke
- furnace
- charging
- ore
- gas
- 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
Links
- 239000000571 coke Substances 0.000 claims description 80
- 238000000034 method Methods 0.000 claims description 30
- 238000000151 deposition Methods 0.000 claims description 4
- 239000010410 layer Substances 0.000 description 41
- 238000009826 distribution Methods 0.000 description 25
- 239000002994 raw material Substances 0.000 description 15
- 238000010586 diagram Methods 0.000 description 10
- 239000002184 metal Substances 0.000 description 8
- 229910052751 metal Inorganic materials 0.000 description 8
- 238000009423 ventilation Methods 0.000 description 8
- 238000005259 measurement Methods 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 6
- 230000004927 fusion Effects 0.000 description 6
- 238000002844 melting Methods 0.000 description 5
- 230000008018 melting Effects 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 230000002093 peripheral effect Effects 0.000 description 3
- 229920005672 polyolefin resin Polymers 0.000 description 3
- 238000006722 reduction reaction Methods 0.000 description 3
- 230000000630 rising effect Effects 0.000 description 3
- 238000004364 calculation method Methods 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 239000002801 charged material Substances 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 238000009827 uniform distribution Methods 0.000 description 2
- 229910000805 Pig iron Inorganic materials 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 230000001174 ascending effect Effects 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 230000001364 causal effect Effects 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000007667 floating Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000011017 operating method Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 238000009491 slugging Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21B—MANUFACTURE OF IRON OR STEEL
- C21B5/00—Making pig-iron in the blast furnace
- C21B5/008—Composition or distribution of the charge
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Manufacture Of Iron (AREA)
Description
【発明の詳細な説明】
本発明は高炉操業におけるコークスの装入方法
に関し、詳細には高炉内における装入原料(コー
クスと鉱石)の積層状態をコークス装入段階で調
整することによつて適正な中心流を確保し高炉操
業の安定に資する方法に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a coke charging method in blast furnace operation, and more specifically, the present invention relates to a method for charging coke in blast furnace operation, and in particular, by adjusting the layered state of charging raw materials (coke and ore) in the blast furnace at the coke charging stage. This article relates to a method for ensuring a stable central flow and contributing to stable blast furnace operation.
近年高炉の大型化に伴ない、高炉1基当りの銑
鉄生産量は飛躍的に増大しているが、大型化の利
点を最大限有効に生かす為には、高炉操業状況を
如何に安定的に維持していくかが重要なポイント
になる。殊に大型高炉では、炉況の悪化に伴なつ
て生産量は大幅に低下し、また次工程に及ぼす影
響も多大である。従つて高炉操業に当たつては
種々の操業条件を巧みにコントロールしなければ
ならないが、就中、炉内における装入原料の分布
を適正に管理することは特に重要である。即ち炉
内に装入された鉱石は、炉内を上昇する高温の還
元ガスによつて加熱されつつ還元されるが、この
加熱と還元を効率よく行なう為には、装入原料
(コークスを含めて)の分布を均一に保ち、すべ
ての鉱石に対して均等に還元ガスを供給する必要
がある。しかし実際の操業においては、原料装入
装置の特性や装入物の堆積特性等各種の因子が影
響し、均一な分布状態を維持することは困難であ
る。特に装入原料の調製工程で生じる物理的、化
学的な変動、或は炉況の悪化等に基因する分布状
態の乱れは、現在の操業法では避け難い。これら
によつて上昇ガスの円周バランスがくずれると、
還元ガスの局部的な偏流が生じ、棚吊り、スリツ
プ、フラツデイング等が多発する。特に棚吊りが
発生すると一時的に送風圧力が上昇し、この風圧
によつて装入原料が吹き上げられるフラツデイン
グ現象やスラツギング現象が現われ、炉況は極端
に悪化する。従つて前記の様な避け難い炉況変化
があつても操業を安定的に維持していく為には、
炉内ガス流を単に均等に分散させるのではなく、
ガス流の一部を一定の領域特に炉心部に集中させ
(以下中心流という)、炉内ガス圧の上昇に対する
安全弁的機能を果させるというのが最近の一般的
判断になつており、これらは経験的にも確認され
ているが、安全な中心流を継続的に得る技術につ
いてはいまのところ満足できるほどには完成され
ていない。即ち例えばベル方式等による通常の装
入方式であると鉱石もコークスも炉壁側から流入
落下されるが鉱石の安息角はコークスのそれに比
べて小さいから炉心側に流動しやすく鉱石層とコ
ークス層の厚み比(ore/coke以下単にO/Cと
いう)は炉心部において高くなる。特にペレツト
化された鉱石を使う高炉では、該ペレツト状鉱石
の安息角が一層小さい為、該鉱石の炉中心部への
流れは顕著であつて、炉中心部のO/Cが更に高
くなる傾向にあり、炉中心部のO/Cを低下させ
たいという要望が特に強く打出されている。上記
課題解決の為の最も一般的な方法として提案され
ているのは、通気性のよいコークスを炉心側に密
に落下装入する方法である。第1図は当該改良提
案に係る原料装入法及び装入原料の分布状態を示
す略図であるが、ベル4を利用して高炉1内にコ
ークス2と鉱石3を交互に装入するに当り、シリ
ンダ5によりアーマープレート6を変位させるこ
とによつて、装入原料の炉内への落下流入位置を
変更する。例えばコークス2を装入するときは、
アーマープレート6を第1図の破線状態にして、
コークス2の落下位置を炉心側とし、一方鉱石3
を装入するときはアーマープレート6を第1図の
実線状態にして鉱石3の落下位置を炉壁側に集中
させる。この方法により炉心部のO/Cが小さく
なり炉心部のコークス比が高まつて中心流の形成
傾向が強まつてくるという成果が得られる。 In recent years, as blast furnaces have become larger, the amount of pig iron produced per blast furnace has increased dramatically, but in order to make the most of the advantages of larger sizes, it is important to keep the operating conditions of the blast furnaces stable. The important point is how to maintain it. Particularly in large blast furnaces, as the furnace conditions deteriorate, the production volume decreases significantly, and the impact on the next process is also significant. Therefore, when operating a blast furnace, various operating conditions must be skillfully controlled, and it is particularly important to appropriately control the distribution of the charging material within the furnace. In other words, the ore charged into the furnace is heated and reduced by the high-temperature reducing gas rising inside the furnace, but in order to efficiently perform this heating and reduction, it is necessary to It is necessary to maintain a uniform distribution of the gas and supply the reducing gas evenly to all ores. However, in actual operations, it is difficult to maintain a uniform distribution state due to various factors such as the characteristics of the raw material charging device and the deposition characteristics of the charged material. In particular, it is difficult to avoid disturbances in the distribution state due to physical or chemical fluctuations occurring during the charging raw material preparation process or deterioration of furnace conditions, etc. with current operating methods. If these things disrupt the circumferential balance of the rising gas,
Localized drift of the reducing gas occurs, and shelving, slipping, flattening, etc. occur frequently. In particular, when shelving occurs, the air blowing pressure temporarily increases, and this wind pressure causes the floating and slugging phenomena in which the charged material is blown up, resulting in extremely poor furnace conditions. Therefore, in order to maintain stable operation even when there are unavoidable changes in furnace conditions as mentioned above, it is necessary to
Rather than simply distributing the furnace gas flow evenly,
It has recently become a general decision to concentrate a portion of the gas flow in a certain area, particularly in the core (hereinafter referred to as the "center flow"), to function as a safety valve against the rise in gas pressure in the reactor. Although this has been confirmed empirically, the technology for continuously obtaining a safe central flow has not yet been fully developed to a satisfactory level. In other words, in a normal charging method such as the bell method, ore and coke flow in and fall from the furnace wall side, but since the angle of repose of ore is smaller than that of coke, it is easy to flow toward the core side and the ore layer and coke layer are separated. The thickness ratio of ore/coke (hereinafter simply referred to as O/C) becomes higher in the reactor core. In particular, in blast furnaces that use pelletized ore, the angle of repose of the pelletized ore is even smaller, so the flow of the ore toward the center of the furnace is significant, and the O/C at the center of the furnace tends to become even higher. There is a particularly strong desire to lower the O/C in the center of the furnace. The most common method proposed to solve the above problem is to drop and charge coke with good ventilation into the reactor core. Figure 1 is a schematic diagram showing the raw material charging method and the distribution of the charged raw materials according to the proposed improvement. , by displacing the armor plate 6 by the cylinder 5, the position at which the charged raw material falls into the furnace is changed. For example, when charging coke 2,
With the armor plate 6 in the state shown by the broken line in Figure 1,
The falling position of coke 2 is set to the core side, while ore 3
When charging the ore, the armor plate 6 is placed in the solid line state shown in FIG. 1 so that the falling position of the ore 3 is concentrated on the furnace wall side. By this method, the O/C in the core is reduced, the coke ratio in the core is increased, and the tendency to form a central flow is strengthened.
しかし上記の方法では、第1図からも明白な様
にO/Cは炉壁部から炉心に向つて徐々に小さく
なるという変化態様であるから、高炉1内の各部
におけるガス流速は第2図のグラフに示す様に炉
壁側から炉心側にかけて徐々に高くなるという漸
増型パターンとなり、後述する様にガス利用率及
び熱効率を十分に高めることができないことが分
かつた。即ち理想的には、たとえば第3図に示す
様に、炉心部のごく限られた領域のみでガス流速
が早く、他の領域ではほぼ均一なガス流速分布を
与えるのが望ましいということが分かつたが、第
3図の様なガス流速分布を得ようとすれば、炉心
部の限られた狭い領域にコークス単味層あるいは
O/Cが極端に小さい原料層を形成し、他の広い
領域にはO/Cが可及的に等しくなる様な原料層
を形成することが必要になる。本発明は正にこの
分野を取扱うものである。 However, in the above method, as is clear from Figure 1, the O/C gradually decreases from the furnace wall toward the core, so the gas flow velocity in each part of the blast furnace 1 is as shown in Figure 2. As shown in the graph, a gradual increase pattern was formed in which the temperature gradually increased from the reactor wall side to the reactor core side, and as will be described later, it was found that the gas utilization rate and thermal efficiency could not be sufficiently increased. In other words, it was found that ideally, as shown in Figure 3, it would be desirable to have a high gas flow rate only in a very limited area of the reactor core, and to provide a nearly uniform gas flow rate distribution in other areas. However, in order to obtain the gas flow velocity distribution as shown in Fig. 3, a single layer of coke or a raw material layer with extremely low O/C would be formed in a narrow area of the reactor core, and a layer of raw material with extremely low O/C would be formed in other wide areas. It is necessary to form a raw material layer in which the O/C ratio is as equal as possible. The present invention deals precisely with this field.
ところで高炉内装入原料は時間の経過と共に順
次降下していくが、下方へ行くに従つてより高温
の還元ガスと遭遇する。従つて原料層は降下につ
れて徐々に昇温され、やがて鉱石固有の軟化温度
に到達すると鉱石層内で軟化現象がはじまり、そ
れまで粒状乃至塊状であつた鉱石類が表面から軟
化しはじめ互いに融着する。軟化融着のはじまつ
た鉱石層は更に降下しつつより高温のガスと遭遇
して更に内部まで軟化されつつ還元反応が進行
し、やがて鉱石固有の溶融滴下開始温度域まで降
下すると軟化鉱石の溶融が始まり、融体となつて
下部コークス層の粒子間をつたいながら更に炉床
に向つて滴下していく。上述の軟化開始から溶融
完了に至るまでの間に存在する鉱石を軟化融着層
と称しているが、この軟化融着層の高炉内におけ
る分布をマクロ的に軟化融着帯と呼んでいる。軟
化融着帯の形状は高炉の操業状況によつて色々変
化するが、前述の中心流が理想的に形成されてい
る場合を想定すると第4図の様に表わすことがで
きる。即ち第4図において、鉱石2とコークス3
は交互に層状をなして装入され順次降下していく
が、前述の還元ガスが中心流を形成して上昇して
いく場合は中央部ほど高温になるから高炉内には
図の如き山形の等温線を描くことができる。そし
て今仮に1200℃を軟化開始温度ラインL1,1450
℃を溶融滴下温度ラインL2とすると、その間に
存在する鉱石が軟化してここに軟化融着層Cが形
成され、全体として山形(通称逆V型)の軟化融
着帯Dが形成されることになる。尚軟化融着層C
では鉱石が軟化して通気抵抗が極めて大きくなつ
ているが、各融着層Cの間に存在するコークスは
高融点であるため装入時の形態(粒状又は塊状)
を維持しており通気抵抗が少ないのでコークスス
リツトEを称されている。従つて羽口8から吹込
まれた高温空気はその直上部まで降下してきたコ
ークスを燃焼させ、生成された還元ガスは矢印で
示す様にコークススリツトEを通り抜けつつ軟化
融着帯Dの上に達し鉱石2及びコークス3を加熱
しながら上昇していく。上記した軟化融着帯Dの
形状は高炉の操業状態特に炉内のガス流量分布に
依存する各高炉固有の内部温度分布によつて決定
され、勿論操業条件のコントロールによつても支
配されるものであるが、高炉休止時の解体調査等
から第5図イ〜ハに示す様な逆V型、W型V型の
3類型に分類され得るものであることが分かつて
いる。 By the way, the raw material in the blast furnace gradually descends over time, and as it goes downward, it encounters higher-temperature reducing gas. Therefore, the temperature of the raw material layer gradually rises as it descends, and when it eventually reaches the softening temperature unique to the ore, a softening phenomenon begins within the ore layer, and the ores, which were previously granular or lumpy, begin to soften from the surface and fuse together. do. The ore layer that has started softening and fusion falls further and encounters higher-temperature gas, and the reduction reaction progresses as it is further softened to the inside, and eventually falls to the temperature range where melting and dripping starts, which is unique to the ore, and the softened ore begins to melt. It begins as a melt and trickles down between particles in the lower coke layer, further dropping towards the hearth. The ore that exists between the start of softening and the completion of melting is called the softened cohesive layer, and the distribution of this softened cohesive layer in the blast furnace is macroscopically called the softened cohesive zone. The shape of the softened cohesive zone changes in various ways depending on the operating conditions of the blast furnace, but assuming that the above-mentioned central flow is ideally formed, it can be expressed as shown in FIG. 4. That is, in Fig. 4, ore 2 and coke 3
The reducing gas is charged in alternating layers and descends one after another. However, when the aforementioned reducing gas forms a central flow and rises, the temperature becomes higher in the center, so the inside of the blast furnace is shaped like a mountain as shown in the figure. Can draw isotherms. And now if 1200℃ is the softening start temperature line L 1 , 1450
If ℃ is the melting dripping temperature line L 2 , the ore existing between them softens and a softened cohesive layer C is formed there, and a chevron-shaped (commonly known as an inverted V-shape) softened cohesive zone D is formed as a whole. It turns out. Furthermore, softened fusion layer C
In this case, the ore has softened and the ventilation resistance has become extremely large, but the coke that exists between each cohesive layer C has a high melting point, so it is difficult to form it at the time of charging (granular or lumpy).
It is called coke slit E because it maintains a low ventilation resistance. Therefore, the high-temperature air blown from the tuyere 8 burns the coke that has fallen directly above it, and the generated reducing gas passes through the coke slit E and onto the softened cohesive zone D as shown by the arrow. It rises while heating ore 2 and coke 3. The shape of the above-mentioned softened cohesive zone D is determined by the operating conditions of the blast furnace, particularly the internal temperature distribution unique to each blast furnace, which depends on the gas flow distribution in the furnace, and is of course also controlled by the control of operating conditions. However, it has been found from dismantling surveys when the blast furnace is shut down that it can be classified into three types: inverted V-type, W-type V-type, and W-type V-type as shown in FIGS. 5A to 5C.
軟化融着帯Dの形状が高炉の操業状態と強い因
果関係にあることは先に述べた通りであるが、逆
にこの様な形状によつて高炉の操業が大きな影響
を受けることも良く知られており、例えば還元ガ
ス利用率や熱交換効率が左右されると共に、スリ
ツプや棚吊りの発生による原料の異常降下原因に
なる場合もある。その為、高炉操業状態を適正に
維持し、且つ安定で効率の良い高炉操業を行う上
では、炉内における軟化融着帯の形状コントロー
ルがもつとも重要な課題であると位置づけられて
おり、高炉操業中の軟化融着帯形状の把握とその
制御法を確立する為に多くの努力が払われてい
る。 As mentioned above, the shape of the softened cohesive zone D has a strong causal relationship with the operational status of the blast furnace, but it is also well known that the operation of the blast furnace is greatly influenced by this shape. For example, this affects the reducing gas utilization rate and heat exchange efficiency, and may also cause abnormal dropping of the raw material due to slipping or hanging on the shelf. Therefore, controlling the shape of the softened cohesive zone inside the furnace is considered to be an important issue in maintaining proper blast furnace operating conditions and performing stable and efficient blast furnace operation. Many efforts have been made to understand the shape of the softened cohesive zone inside the material and to establish methods for its control.
本発明はこの様な状況に鑑みてなされたもので
あつて、中心流を確保することによつて軟化融着
帯形状を最適の形態に保持することができる様な
原料(特にコークス)の装入方法を提供すべく研
究した成果である。即ち本発明は、高炉に対して
鉱石とコークスを交互に装入する場合におけるコ
ークス装入方法であつて、各チヤージにおけるコ
ークスの装入を経時的に少なくとも2系列に分
け、当該チヤージの総装入コークス量の92〜98.5
重量%を前装入の鉱石層を全て覆う様に装入し、
最後の装入系列では当該チヤージの総装入コーク
ス量の8〜1.5重量%を炉中心部へ集中的に装入
することにより、炉中心部のO/Cを炉中心部以
外の領域のO/Cよりも実質的に小さくなる様に
堆積させる点に要旨が存在するものである。 The present invention was made in view of these circumstances, and it is a method of loading raw materials (especially coke) that can maintain the softened cohesive zone shape in an optimal form by ensuring a central flow. This is the result of research aimed at providing a method for entering the system. That is, the present invention is a coke charging method in which ore and coke are alternately charged into a blast furnace, in which the coke charging in each charge is divided over time into at least two series, and the total charging of the charge is 92 to 98.5 of coke amount
Charge % by weight so as to cover all the ore layer previously charged,
In the last charging series, 8 to 1.5% by weight of the total amount of coke charged in the charge is intensively charged into the furnace center, thereby reducing the O/C in the furnace center to the O/C in the area other than the furnace center. The gist lies in depositing the metal so that it is substantially smaller than /C.
以下研究の経緯に触れつつ本発明の構成及び作
用降下を明らかにしていく。 The structure and effects of the present invention will be clarified below while referring to the background of the research.
まず本発明者等は軟化融着帯の形状をオンライ
ンでより正確に把握することが前提になると考
え、第4図の軟化開始温度ラインL1(1200℃)の
実炉におけるプロフイルを推定しようと考え種々
検討を行なつたのでこの点から説明する。 First, the inventors thought that it would be necessary to more accurately grasp the shape of the softening cohesive zone online, and tried to estimate the profile of the softening start temperature line L 1 (1200°C) in Fig. 4 in an actual furnace. I have thought about this and have conducted various studies, so I will explain from this point.
即ち高炉装入原料が前述の様に層状構造である
ことに着目しコークス層と鉱石層の各層において
各々熱収支と物質収支を計算すれば、炉内の高さ
方向温度分布を推算することができると考えた。
つまり炉内iチヤージ位置まで降下してきた各層
は、ガス温度(Ti)の雰囲気で装入間隔(H時
間)の時間長さに亘つて加熱され、次いでi+1
チヤージ位置へ移行する。そしてiチヤージ位置
におけるコークス層と鉱石層の加熱式は、いずれ
も(1)式で表わされる。 In other words, by focusing on the layered structure of the blast furnace charging material as mentioned above and calculating the heat balance and mass balance in each layer of the coke layer and the ore layer, it is possible to estimate the temperature distribution in the height direction inside the furnace. I thought it could be done.
In other words, each layer that has descended to the charge position i in the furnace is heated in an atmosphere at the gas temperature (Ti) for the charging interval (H time), and then heated to the charge position i+1.
Move to charge position. The heating equations for the coke layer and the ore layer at the i charge position are both expressed by equation (1).
d/dθ(ρbCst)=a hp(Ti−t)
+
〓j
Rj(−ΔHj) (1)
ここで
ρb:嵩密度
Cs:固体比熱
t:固体温度
a:伝熱比表面積
hp:ガス〜固体間熱伝達係数
Ti:iチヤージ位置におけるガス温度
Rj:コークス層もしくは鉱石層内で反応
するj成分の反応速度
ΔHi:コークス層もしくは鉱石層内で反応
するj成分の反応熱
θ:時間
θ=0、t=ti−1の初期条件下で、(1)式を装
入間隔H時間まで積分するとiチヤージ位置にお
ける各層固体の到達温度tiが得られる。 d/dθ (ρbCst) = a hp (Ti-t) + 〓 j Rj (-ΔHj) (1) where ρb: Bulk density Cs: Solid specific heat t: Solid temperature a: Heat transfer specific surface area hp: Gas to solid Ti: Gas temperature at i charge position Rj: Reaction rate of component j reacting in the coke layer or ore layer ΔHi: Heat of reaction of component j reacting in the coke layer or ore layer θ: Time θ=0 , t=ti-1, by integrating equation (1) up to the charging interval H time, the temperature ti reached by the solid in each layer at the i charge position can be obtained.
一方iチヤージ位置の各層の総括熱収支から、
iチヤージ位置の各層へ流入するガス温度(Ti
+1)は(2)式で算出される。 On the other hand, from the overall heat balance of each layer at the i charge position,
i Gas temperature flowing into each layer at the charge position (Ti
+1) is calculated using equation (2).
Ti-1=Ti+Gi(ti−ti-1)
+
〓j
Mj(−ΔHj) (2)
ここで
Gi=Δk Fs ρb Cs/ΔFg ρg Cg (k=c,o)
Δk(k=c,o):コークス層、鉱石層の層
厚、Δ=Δc+Δo
Fs:装入物降下量
Fg:ガス流量
ρb:ガス密度
Cg:ガス比熱
Mj:反応に関するj成分の反応量
またi−1、iチヤージ間の反応に伴なうガス
成分[X(j) i]の変化は、総括物質収支から(3)式の
ように求められる。 T i-1 = Ti + Gi (ti-t i-1 ) + 〓 j Mj (-ΔHj) (2) where Gi = Δk Fs ρb Cs/ΔFg ρg Cg (k=c, o) Δk (k=c, o): Thickness of coke layer and ore layer, Δ=Δc+Δo Fs: Falling amount of charge Fg: Gas flow rate ρb: Gas density Cg: Gas specific heat Mj: Reaction amount of j component related to reaction Also, i-1, i charge The change in gas component [X (j) i ] due to the reaction between
X(j) i=X(j) i-1−mjMj (3)
mj:化学量論係数
次に炉頂もしくはある指定されたiチヤージ位
置のガス温度Tiを(1)式に代入して積分すること
により固体温度tiが得られ、更に(2)式、(3)式から
次のチヤージのガス温度と成分が算出できる。そ
して(2)式で得られたガス温度を再び(1)式に代入し
てiを更新する、というように、(1)〜(3)式の計算
を繰り返していくことにより、炉内各チヤージ位
置の温度、すなわち高さ方向の温度分布を算出す
ることができる。 X (j) i = X (j) i-1 −mjMj (3) mj: Stoichiometric coefficient Next, substitute the gas temperature Ti at the furnace top or a certain designated i charge position into equation (1) and integrate it. By doing this, the solid temperature ti can be obtained, and the gas temperature and components of the next charge can be calculated from equations (2) and (3). Then, by substituting the gas temperature obtained in equation (2) again into equation (1) and updating i, by repeating the calculations of equations (1) to (3), The temperature at the charge position, that is, the temperature distribution in the height direction can be calculated.
又高炉を半径方向にn分割し、各分割領域毎に
(1)〜(3)式を適用して上述の計算手順を繰返すこと
により炉内半径方向及び高さ方向の温度分布を求
めることができる。尚各分割領域毎のコークス層
と鉱石層の高さ方向位置と層厚は、炉頂部におけ
る半径方向層厚分布の測定結果に各層の降下に伴
う収縮を加味して算出する。半径方向に5分割し
た場合の各分割領域の高さ方向温度分布の計算例
を第6図に示す。第6図に示す様に、任意に指定
された温度(例えば1200℃)の炉内位置を結ぶこ
とによりその等温線を求めることができる。 In addition, the blast furnace is divided into n parts in the radial direction, and each divided area is
By applying equations (1) to (3) and repeating the above calculation procedure, the temperature distribution in the furnace radial direction and height direction can be determined. The height direction position and layer thickness of the coke layer and ore layer for each divided area are calculated by adding the contraction caused by the descent of each layer to the measurement results of the radial layer thickness distribution at the top of the furnace. FIG. 6 shows an example of calculating the temperature distribution in the height direction of each divided area when divided into five areas in the radial direction. As shown in FIG. 6, by connecting the positions in the furnace at an arbitrarily specified temperature (for example, 1200° C.), its isothermal line can be determined.
(1)〜(3)式を実操業に精度よく適合できる様にす
る必要があるので、炉内反応速度[(1)式中Rj]
については、多点同時測定による炉内温度分布の
実測(特公昭57−48621等)結果が計算結果と一
致するように決定する。尚(1)〜(3)式の計算は、炉
頂部から始めることも可能であるが、炉頂部は融
着帯から離れていること、炉頂部の計測情報は装
入物の堆積傾斜角に帰因するガスの偏流の影響を
受けて炉内状況を必ずしも反映しないこと、等の
理由により、1000℃以上の高温域の状況及び鉱石
類の融着開始位置を精度よく推定することは困難
である。従つて(1)〜(3)式の計算開始位置として
は、融着帯に近くてしかも半径方向のガス温度と
ガス成分がいずれも測定できる計測装置の設置位
置を採用する。 Since it is necessary to adapt equations (1) to (3) accurately to actual operation, the in-furnace reaction rate [Rj in equation (1)]
Regarding the above, it is determined so that the actual measurement results (Japanese Patent Publication No. 57-48621, etc.) of the temperature distribution in the furnace by simultaneous measurement at multiple points match the calculated results. It is also possible to calculate equations (1) to (3) starting from the top of the furnace, but the top of the furnace is far from the cohesive zone, and the measurement information at the top of the furnace depends on the deposition angle of the charge. It is difficult to accurately estimate the situation in the high-temperature range of 1000℃ or higher and the starting position of ore fusion because it does not necessarily reflect the situation inside the furnace due to the influence of gas drift. be. Therefore, as the starting position for calculating equations (1) to (3), the installation position of the measuring device that is close to the cohesive zone and that can measure both the gas temperature and gas components in the radial direction is adopted.
第7図イに示すように1200℃等温線の推算結果
と実測結果が一致するように決定したパラメータ
ー(Rj)を用いて、操業条件が大きく異なる場
合に推定した1200℃等温線と実測したそれを第7
図ロに比較して示すが、よい一致を示している。 As shown in Figure 7A, using the parameter (Rj) determined so that the estimated result of the 1200°C isotherm line and the actual measurement result match, the estimated 1200°C isotherm line and the actually measured one when the operating conditions are significantly different are used. The seventh
A comparison is shown in Figure B, which shows good agreement.
このようにして推定した1200℃等温線を炉内に
おける鉱石類の融着開始線、すなわち軟化融着帯
の外部形状とみなし、第8図に示すようにこの
1200℃等温線で高炉を上部と下部に分割する。こ
の等温線より上部の堆積層体積をV1とし、軟化
融着帯を含む下部の体積をV2とする。さらに高
炉最周辺部(鉄皮部分)の1200℃位置と羽口中心
軸の位置との間の距離をHwとする。 The 1200°C isotherm estimated in this way is regarded as the line at which the fusion of ores begins to coalesce in the furnace, that is, the external shape of the softened cohesive zone, and this is shown in Figure 8.
Divide the blast furnace into upper and lower parts using the 1200℃ isotherm. Let the volume of the deposited layer above this isotherm be V1 , and let the volume below including the softened cohesive zone be V2 . Furthermore, the distance between the 1200°C position of the most peripheral part of the blast furnace (shell part) and the position of the central axis of the tuyere is defined as Hw.
次にV1/(V1+V2)とガス利用率[ηcp]の関
係、Hwと炉壁最大熱負荷を受けるスラーブクー
ラーの位置の関係及びHwと溶銑中のSi濃度の関
係をそれぞれ第9〜11図(斜線部は管理範囲を
示す)に示す様に求めたので以下その背景につい
て説明する。これらは軟化融着帯の形状が逆V型
とW型である場合のデータであるが、まず第9図
によるとV1/(V1+V2)の値、即ち相対的には
1200℃ラインより上方の原料体積(粒状又は塊状
域体積)が大きいほどガス利用率が大きいことが
分かる。但しこの傾向は逆V型とW型の間で殆ん
ど有意の差が認められなかつた。 Next, the relationship between V 1 / (V 1 + V 2 ) and the gas utilization rate [η cp ], the relationship between Hw and the position of the slab cooler that receives the maximum heat load on the furnace wall, and the relationship between Hw and the Si concentration in the hot metal are calculated. Since the values were obtained as shown in Figures 9 to 11 (the shaded area indicates the management range), the background thereof will be explained below. These are data when the shape of the softened cohesive zone is an inverted V shape and a W shape, but first, according to Figure 9, the value of V 1 / (V 1 + V 2 ), that is, relatively
It can be seen that the larger the raw material volume (volume of granular or lumpy region) above the 1200°C line, the larger the gas utilization rate. However, there was almost no significant difference in this tendency between the inverted V type and the W type.
一方第10図は横軸にHw、縦軸に炉壁熱負荷
の最大位置(鉄皮温度又は耐火壁温度の分布より
判定)をとつて両者の対比をしたものである。本
図において1:1の関係を示す45゜の勾配線を基
準にすると、W型では概して下にあつてHwは最
大熱負荷位置よりかなり高い位置にあることが分
かり、他方逆V型では概して基準勾配線より上に
あつてHwは最大熱負荷位置より下方にあること
が分かる。換言すると、W型の場合は炉壁部融着
帯位置より下方の炉壁に熱負荷が大きくなつてお
り、これは第12図イに示す様に羽口から出た高
温ガスが融着帯の下方突出岬によつて分断されて
炉心方向と羽口直上方向の2方向に分かれて上昇
し、炉壁に沿う上昇ガス流が融着帯より下方の炉
壁を強く加熱するからであると思われる。これに
対し逆V型では第12図ロに示す様に羽口から出
た高温ガスは融着帯の斜面に沿つて炉中心方向に
深く流れ込み、前第4図で説明したコークススリ
ツトを通して上部塊状帯に分配され、この時点で
ガス流の影響が炉壁部に現われるからであると思
われる。しかるに高炉操業においては溶銑温度の
低下を防ぐという意味から炉中心部は十分高温に
維持されていることが望ましく、又炉壁が冷却盤
の損傷が溶損を防ぐという意味から炉周辺部特に
羽口直上部の温度は可及的に低いことが望ましい
とされているから、結局融着帯形状としては上記
要望を満足する逆V型が好ましいという結論を導
くことができる。 On the other hand, FIG. 10 shows a comparison between Hw on the horizontal axis and the maximum position of furnace wall heat load (determined from the distribution of shell temperature or refractory wall temperature) on the vertical axis. Based on the 45° slope line that shows a 1:1 relationship in this figure, it can be seen that in the W type, Hw is generally at the bottom and at a position considerably higher than the maximum heat load position, while in the inverted V type, it is generally at the bottom. It can be seen that Hw is above the reference gradient line and below the maximum heat load position. In other words, in the case of the W-type, the heat load is greater on the furnace wall below the cohesive zone position, and this is because the high temperature gas coming out of the tuyere reaches the cohesive zone as shown in Figure 12A. This is because the gas flow is divided by the downward protruding cape and rises in two directions: towards the reactor core and directly above the tuyere, and the rising gas flow along the reactor wall strongly heats the reactor wall below the cohesive zone. Seem. On the other hand, in the inverted V type, as shown in Figure 12 (b), the high-temperature gas coming out of the tuyeres flows deeply toward the center of the furnace along the slope of the cohesive zone, and passes through the coke slits explained in Figure 4 above to the upper part. This is thought to be because the gas is distributed into a lumpy zone, and at this point the influence of the gas flow appears on the furnace wall. However, in blast furnace operation, it is desirable to maintain a sufficiently high temperature in the center of the furnace in order to prevent a drop in hot metal temperature, and in order to prevent the furnace wall from melting due to damage to the cooling disk, it is desirable to maintain the temperature in the furnace periphery, especially the blade. Since it is said that it is desirable that the temperature directly above the mouth be as low as possible, it can be concluded that the shape of the cohesive zone is preferably an inverted V shape that satisfies the above requirements.
次に第11図はHwを横軸、溶銑中のSi濃度を
縦軸にとつて両者の関係を見たものであるが、W
型及び逆V型の如何を問わず低Si化の為にはHw
を低い位置にする方が良いということが分かる。
但し同図のHwに着目すると、W型のものより逆
V型の方が低くなる傾向にあり、従つてSi濃度も
低下させ易い様であり、低Si化の達成という観点
からしても逆V型が望ましいという結論が得られ
る。 Next, Figure 11 shows the relationship between Hw on the horizontal axis and the Si concentration in hot metal on the vertical axis.
Regardless of type or inverted V type, Hw is required for low Si.
It turns out that it is better to lower the position.
However, if we focus on Hw in the same figure, it tends to be lower in the inverted V type than in the W type, and therefore it seems easier to lower the Si concentration. The conclusion is that a V-type is preferable.
以上述べた様に融着帯形状としては逆V型が好
まれるが、中でもガス利用率という観点からは
V1/(V1+V2)を大きくする方が好ましく、炉
壁の保護及び溶銑に低Si化という観点からはHw
を小さくする方が好ましい。即ち逆V型の融着帯
形状を高炉内の可及的低い位置に形成する様な操
業コントロールを行なうのが好ましいということ
が分かつた。そしてその目安としては、第9図か
ら
V1/V1+V2≧0.52 (4)
又第11図からは
Hw≦7.5m (5)
という2つの条件を設定することができる旨理解
できた。 As mentioned above, an inverted V shape is preferred as the cohesive zone shape, but from the viewpoint of gas utilization rate,
It is preferable to increase V 1 / (V 1 + V 2 ), and from the viewpoint of protecting the furnace wall and reducing Si in the hot metal, Hw
It is preferable to make it smaller. That is, it has been found that it is preferable to control the operation so as to form an inverted V-shaped cohesive zone at the lowest possible position within the blast furnace. As a guideline, it was understood that two conditions can be set: V 1 /V 1 +V 2 ≧0.52 (4) from Fig. 9, and Hw≦7.5m (5) from Fig. 11.
ところで融着帯の形状及び位置をコントロール
するに当つては、まず逆V型への形状コントロー
ルを第一義的に置くべきであるという考えから、
高炉内の温度分布が第4図に示した様な山形にな
る様なガス流コントロールを中心に据えて検討し
た。 By the way, when controlling the shape and position of the cohesive zone, the first priority should be to control the shape to an inverted V shape.
The study focused on controlling the gas flow so that the temperature distribution inside the blast furnace becomes mountain-shaped as shown in Figure 4.
ガス流分布を支配する要因は、前記各説明から
理解できる様に鉱石層とコークス層の分布であ
り、上記目的に適う為には中心流の確保がどうし
ても必要である。その為には炉内堆積層の通気抵
抗を炉中心部で小さくなる様に工夫しなければな
らず、しかもこれを前述(第1図)のアーマープ
レート法より優れた方法で達成することが必要に
なる。そこで本発明者等は抜本的な対策を立案し
モデル容器によつて検討したところ、コークスの
装入操業を少なくとも2つの系列に分け、初期の
装入操業系列では当該チヤージの総投入コークス
量の大部分を前装入の鉱石層が全て覆われる様に
装入し、最後の装入操業系列で当該チヤージの総
装入コークス量の残部を炉中心部へ集中的に装入
した場合には第13図に示す様な積層状態が得ら
れることを確認した。即ち第13図においてコー
クスは経時的にA,Bの2系列に分けて装入され
るが鉱石3とコークスAはベルによる通常装入方
式によるものであつて鉱石3の安息角がコークス
Aの安息角より小さいことのために、もしコーク
スBの存在がなければ炉中心部における鉱石3の
厚みはコークスAの厚みより大きくなり(O/C
が大きくなり)、炉中心部の通気抵抗が大きくな
つて中心流は得られない。しかし本発明の装入法
では、コークスAの装入が終つた後でコークスA
の中央凹部を埋めて更に積上げる様にコークスB
を集中的に投入しているのでその後で装入される
鉱石3は既に炉中心部がコークスBで占領された
かたちになつている為炉中心部に入る量は極めて
少なくなり炉中心部のO/Cは非常に小さなもの
となり中心流の確保に大きく貢献することができ
る。即ちこの装入方式はコークスの安息角が比較
的大きいことを積極的に利用したものであり、コ
ークスAの装入によつて生じた炉中心部の凹部の
上にコークスBを追加装入してもコークスBの小
山が扁平にくずれることはないので、当該チヤー
ジにおけるコークスB/A分配比はそれほど大き
くとる必要はなく、又コークスBの装入による前
記効果は極めて安定したものとなる。尚本発明の
効果は、コークスの装入を行なうたびごとに上記
の様な分割装入を行なうことで最大限に発揮され
るが、上記制御によつて炉況が安定してきた場合
や他の操炉条件によつて炉況に変化が生じた場合
は、本発明の数字条件をはずれた装入方式、又は
通常のコークス装入方式を多少組合わせることが
あつてもよい。 As can be understood from the above explanations, the factors governing the gas flow distribution are the distributions of the ore layer and the coke layer, and in order to meet the above objectives, it is absolutely necessary to ensure a central flow. To achieve this, it is necessary to devise a method to reduce the ventilation resistance of the deposited layer in the furnace at the center of the furnace, and it is necessary to achieve this using a method superior to the armor plate method described above (Figure 1). become. Therefore, the present inventors devised a drastic countermeasure and studied it using a model vessel, and found that the coke charging operation was divided into at least two series, and in the initial charging operation series, the total amount of coke input for the charge was If most of the coke is charged so as to cover the entire ore layer of the pre-charging operation, and the remainder of the total amount of coke charged in the charge is intensively charged to the center of the furnace in the last charging operation series, It was confirmed that a laminated state as shown in FIG. 13 could be obtained. That is, in Fig. 13, coke is charged over time in two series, A and B, but ore 3 and coke A are charged by the normal Bell charging method, and the angle of repose of ore 3 is different from that of coke A. Because it is smaller than the angle of repose, if there were no coke B, the thickness of ore 3 in the furnace center would be greater than the thickness of coke A (O/C
), the ventilation resistance at the center of the furnace becomes large, and a central flow cannot be obtained. However, in the charging method of the present invention, after the charging of coke A is completed, coke A
Fill the center recess of the coke B and stack it further.
Since Ore 3 is charged in a concentrated manner, the center of the furnace is already occupied by coke B, so the amount that enters the center of the furnace is extremely small and the amount of O in the center of the furnace is reduced. /C becomes very small and can greatly contribute to securing the central flow. In other words, this charging method actively utilizes the relatively large angle of repose of coke, and additionally charges coke B onto the depression in the center of the furnace created by charging coke A. Even if the coke B is charged, the small mountain of coke B will not flatten, so the coke B/A distribution ratio in the charge does not need to be so large, and the effect of charging coke B will be extremely stable. The effects of the present invention can be maximized by performing split charging as described above each time coke is charged, but if the furnace conditions have stabilized due to the above control or other conditions If the furnace conditions change due to furnace operation conditions, a charging method that deviates from the numerical conditions of the present invention or a normal coke charging method may be combined to some extent.
尚コークスBを炉中心部へ集中的に装入してコ
ークスA上に小山を作る手段としては本発明にお
いて特に制限を加えないが、代表的な手段を例示
すると、第14図に示す様にベル4にコークスB
の専用落下パイプ9を内蔵する方式、第15図に
示す如く、高炉鉄皮の上方を貫通してコークスB
供給パイプ10を挿設しその先端を炉中心部に臨
ませる方式等を例示することができる。 The method of charging coke B intensively into the center of the furnace to form a mound on coke A is not particularly limited in the present invention, but a typical method is as shown in FIG. 14. Coke B in Bell 4
As shown in Fig. 15, the coke B passes through the upper part of the blast furnace shell.
An example is a method in which the supply pipe 10 is inserted and its tip faces the center of the furnace.
次にコークスBの装入量を全量(A+B)に対
して2〜8重量%が良いと定めた理由について説
明する。16図はコークスBの装入比率を8.3〜
1.4重量%の間で適宜変化させたときの炉体半径
方向に見た(1)O/C分布(通気抵抗分布)、(2)炉
頂の排ガス温度分布、(3)軟化融着帯形状、(4)
V1/(V1+V2)比、及び(5)Hwを示すものであ
り、0.6m3試験炉中にコークス(10〜20mmφ)と
オレフイン樹脂(鉱石の代用、6.5mmφ)を本発
明方法に従つて装入し、下方より170℃の空気を
吹上げて実験した。尚オレフイン樹脂の融着開始
温度は90℃であり、コークス/オレフイン樹脂の
体積比は実炉に合わせて3.14とした。尚前記(1)〜
(5)の各項目のうち、(5)のHwについては、実炉換
算値である。第16図を詳細に検討すると、コー
クスBが8.3%のときは、融着帯形状が逆V型に
なつているもののV1/(V1+V2)が0.515であつ
て前記(4)式で示した条件を満足しておらず、また
炉頂の温度分布も第2図で示したのと同様のなだ
らかな曲線を描いており、更に炉中心部側が比較
的広い領域にわたつて通気抵抗が零になつてお
り、却つて中心部でガスの吹抜けを生じる恐れが
あつてそれぞれの点より見てもガス利用率が低く
なることが予測された。他方コークスBが1.4%
のときはV1/(V1+V2)の項目のみが前記各条
件を満足しているだけであつて炉中心部の通気抵
抗がかなり高いこと、炉頂温度も中心部で高くな
いこと、融着帯形状が完全なW型になつているこ
と、Hwの実炉換算値が前記(5)式の条件を満足し
ていないこと等の各理由から、中心流が得られな
いと共に、融着帯形状が悪くなつて炉壁の熱負荷
部が下方へ下り、且つ溶銑Siの低下も期待されな
い。 Next, the reason why it is determined that the charging amount of coke B is preferably 2 to 8% by weight based on the total amount (A+B) will be explained. Figure 16 shows the charging ratio of coke B from 8.3 to
(1) O/C distribution (ventilation resistance distribution) in the radial direction of the furnace body, (2) exhaust gas temperature distribution at the top of the furnace, and (3) shape of softened cohesive zone when appropriately varied between 1.4% by weight. ,(Four)
This shows the V 1 /(V 1 + V 2 ) ratio and (5) Hw. Coke (10 to 20 mmφ) and olefin resin (substitute for ore, 6.5 mmφ) were placed in a 0.6 m 3 test furnace using the method of the present invention. The experiment was carried out by charging air at 170°C from below. The fusion start temperature of the olefin resin was 90°C, and the volume ratio of coke/olefin resin was 3.14 in accordance with the actual furnace. Note that (1) above
Among the items in (5), Hw in (5) is the actual furnace equivalent value. A detailed study of FIG. 16 reveals that when coke B is 8.3%, the cohesive zone has an inverted V shape, but V 1 /(V 1 +V 2 ) is 0.515, and the above formula (4) The conditions shown in Figure 2 are not satisfied, and the temperature distribution at the top of the furnace is a gentle curve similar to that shown in Figure 2. Furthermore, the center of the furnace has a relatively wide area with ventilation resistance. It was predicted that the gas utilization rate would be low from each point of view, as there was a risk of gas leakage occurring in the center. On the other hand, Coke B is 1.4%
In this case, only the item V 1 / (V 1 + V 2 ) satisfies each of the above conditions, and the ventilation resistance at the center of the furnace is quite high, and the temperature at the top of the furnace is not high at the center. For various reasons, such as the cohesive zone having a perfect W-shape and the actual furnace equivalent value of Hw not satisfying the condition of equation (5) above, a central flow cannot be obtained and the fusion The shape of the belt deteriorates, the heat load part of the furnace wall goes downward, and no reduction in hot metal Si is expected.
これらに対しコークスBが7.5%,6.7%,5
%,2.5%の各実験例では前記各条件が満足され
ると共に良好な融着帯形状(逆V字型)及びその
位置、並びに中心流が確保されており、しかもガ
ス利用率や炉壁への熱負何位置も満足すべき状況
にある。 In contrast, coke B was 7.5%, 6.7%, and 5%.
% and 2.5%, the above-mentioned conditions were satisfied, and a good cohesive zone shape (inverted V-shape) and its position, as well as a central flow were secured, and the gas utilization rate and furnace wall Both positions are in satisfactory condition.
本発明は上記の如く構成され炉中心部のO/C
を有意義に低下させることができているから、高
炉内の融着帯がその形状及び高さ位置において最
適のプロフイルを呈すると共に安定でガス利用率
の面で不都合のない中心流を示すことができる様
になり、又溶銑の低Si化、炉壁熱負何の軽減等、
高炉操業の安定、溶銑の品質向上、炉体保護等、
各方面において満足することのできる結果が得ら
れる様になつた。 The present invention is configured as described above, and the O/C at the center of the furnace is
As a result, the cohesive zone in the blast furnace can exhibit an optimal profile in terms of its shape and height position, and it can also exhibit a stable central flow without any disadvantages in terms of gas utilization. In addition, it is possible to reduce the Si content of hot metal, reduce the heat load on the furnace wall, etc.
Stable blast furnace operation, improved quality of hot metal, protection of the furnace body, etc.
Satisfactory results were obtained in all aspects.
第1図は高炉に対する従来の原料装入法を示す
概略説明図、第2図はそのときの炉頂ガスの流速
分布を示すグラフ、第3図は理想的な炉頂ガス流
速分布を示すグラフ、第4図は高炉の内面を概念
的に示す説明図、第5図イ,ロ,ハは融着帯形状
の模式図、第6図は高炉を半径方向に5分割した
場合の各分割領域ごとの高さ方向温度分布の推算
例を示すグラフ、第7図は1200℃等温線の推算結
果と実測値の比較を示す高炉の右半分断面説明図
で、第7図イは推算と実測が一致する様にパラメ
ーター(Rj)を決定したもの、第7図ロは決定
されたRjを用いて推算した結果と実測の比較を
示すものである。又第8図は1200℃等温線による
融着帯の上部V1と下部V2の各体積及び周辺部融
着帯位置Hwの定義を示す説明図、第9図はV1/
(V1+V2)とガス利用率の関係を示すグラフ、第
10図はHwとステーブクーラー最大熱負何位置
の関係を示すグラフ、第11図はHwと溶銑中の
Si濃度の関係を示すグラフ、第12図イ,ロは融
着帯形状とガスの上昇経路を示す高炉の右半分断
面説明図、第13図は本発明によるコークスの分
割装入とO/Cの関係を示す説明図、第14,1
5図はコークスの分割投入方式を示す実験例の説
明図、第16図はモデル実験の結果を示す説明図
である。
1……高炉、2,A,B……コークス、3……
鉱石、D……軟化融着帯、E……コークススリツ
ト。
Figure 1 is a schematic explanatory diagram showing the conventional method of charging raw materials into a blast furnace, Figure 2 is a graph showing the top gas flow velocity distribution at that time, and Figure 3 is a graph showing the ideal furnace top gas flow velocity distribution. , Fig. 4 is an explanatory diagram conceptually showing the inner surface of the blast furnace, Fig. 5 A, B, and C are schematic diagrams of the cohesive zone shape, and Fig. 6 shows each divided area when the blast furnace is divided into five in the radial direction. Figure 7 is a cross-sectional diagram of the right half of a blast furnace showing a comparison between the estimated results of the 1200°C isotherm and actual measurements. The parameters (Rj) were determined so that they matched, and Figure 7 (b) shows a comparison between the estimated results using the determined Rj and the actual measurements. Also, Fig. 8 is an explanatory diagram showing the definition of the volumes of the upper V 1 and lower V 2 of the cohesive zone and the position Hw of the peripheral cohesive zone based on the 1200°C isotherm, and Fig. 9 is an explanatory diagram showing the definition of the volume of the upper V 1 and lower V 2 of the cohesive zone and the position Hw of the peripheral cohesive zone.
(V 1 + V 2 ) and gas utilization rate. Figure 10 is a graph showing the relationship between Hw and the maximum heat negative position of the stave cooler. Figure 11 is a graph showing the relationship between Hw and the maximum heat negative position of the stave cooler.
A graph showing the relationship between Si concentration, Figures 12A and 12B are explanatory cross-sectional views of the right half of the blast furnace showing the shape of the cohesive zone and the ascending path of gas, and Figure 13 is the partial coke charging and O/C according to the present invention. Explanatory diagram showing the relationship, No. 14, 1
FIG. 5 is an explanatory diagram of an experimental example showing a method of dividing coke injection, and FIG. 16 is an explanatory diagram showing the results of a model experiment. 1... Blast furnace, 2, A, B... Coke, 3...
Ore, D...Softened cohesive zone, E...Coke slit.
Claims (1)
る場合におけるコークス装入方法であつて、各チ
ヤージにおけるコークスの装入を経時的に少なく
とも2系列に分け、当該チヤージの総装入コーク
ス量の92〜98.5重量%を前装入の鉱石層を全て覆
う様に装入し、最後の装入系列では当該チヤージ
の総装入コークス量の8〜1.5重量%を炉中心部
へ集中的に装入することにより、炉中心部の
ore/coke比を炉中心部以外の領域のore/coke
比よりも実質的に小さくなる様に堆積させること
を特徴とする高炉へのコークス装入方法。1. A coke charging method when ore and coke are charged alternately to a blast furnace, in which the coke charging in each charge is divided over time into at least two series, and the total amount of coke charged in the charge is 92 to 98.5% by weight of coke is charged so as to cover the entire ore layer of the pre-charging, and in the last charging series, 8 to 1.5% by weight of the total amount of coke charged in the charge is intensively charged to the center of the furnace. The center of the furnace
The ore/coke ratio in the area other than the center of the furnace
A method for charging coke into a blast furnace, characterized by depositing coke so that the coke ratio is substantially smaller than the coke ratio.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP16227383A JPS6056003A (en) | 1983-09-02 | 1983-09-02 | Method for charging coke into blast furnace |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP16227383A JPS6056003A (en) | 1983-09-02 | 1983-09-02 | Method for charging coke into blast furnace |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6056003A JPS6056003A (en) | 1985-04-01 |
| JPS649373B2 true JPS649373B2 (en) | 1989-02-17 |
Family
ID=15751325
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP16227383A Granted JPS6056003A (en) | 1983-09-02 | 1983-09-02 | Method for charging coke into blast furnace |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6056003A (en) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BR8704362A (en) * | 1986-08-26 | 1988-04-19 | Kawasaki Steel Co | PROCESS AND SYSTEM FOR PERFORMING REDUCING FUSION OPERATION |
| JPH0637649B2 (en) * | 1987-09-03 | 1994-05-18 | 株式会社神戸製鋼所 | Control method of core reducing agent layer in blast furnace operation |
| JPS6465219A (en) * | 1987-09-03 | 1989-03-10 | Kobe Steel Ltd | Method for controlling furnace core packing structure |
| JPS6465209A (en) * | 1987-09-03 | 1989-03-10 | Kobe Steel Ltd | Method for controlling furnace core solid reducing agent layer in blast furnace operation |
| JPS6465213A (en) * | 1987-09-03 | 1989-03-10 | Kobe Steel Ltd | Method for charging raw material to axial center part of blast furnace |
| JPS6465212A (en) * | 1987-09-03 | 1989-03-10 | Kobe Steel Ltd | Method for operating blast furnace |
| JP2600803B2 (en) * | 1988-05-18 | 1997-04-16 | 住友金属工業株式会社 | Blast furnace raw material charging method |
| JPH0692608B2 (en) * | 1989-02-28 | 1994-11-16 | 株式会社神戸製鋼所 | Blast furnace operation method |
| JPH03202719A (en) * | 1989-12-29 | 1991-09-04 | Hoya Corp | Fused-glass liquid level meter |
| JPH0627283B2 (en) * | 1990-06-13 | 1994-04-13 | 株式会社神戸製鋼所 | Method of charging raw material into blast furnace |
| JP7680243B2 (en) | 2021-03-31 | 2025-05-20 | 株式会社神戸製鋼所 | Pig iron production method |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5437004A (en) * | 1977-08-30 | 1979-03-19 | Kawasaki Steel Co | Controlling method for properly adjusting thickness of charging materials in blast furnace |
| JPS55104407A (en) * | 1979-02-05 | 1980-08-09 | Kobe Steel Ltd | Blast furnace operating method |
-
1983
- 1983-09-02 JP JP16227383A patent/JPS6056003A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6056003A (en) | 1985-04-01 |
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