JPH0567686B2 - - Google Patents
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- Publication number
- JPH0567686B2 JPH0567686B2 JP19906485A JP19906485A JPH0567686B2 JP H0567686 B2 JPH0567686 B2 JP H0567686B2 JP 19906485 A JP19906485 A JP 19906485A JP 19906485 A JP19906485 A JP 19906485A JP H0567686 B2 JPH0567686 B2 JP H0567686B2
- Authority
- JP
- Japan
- Prior art keywords
- sintering
- layer
- fixed carbon
- coke
- raw material
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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Description
(産業上の利用分野)
本発明は、製鉄原料の焼結法、特に2段点火式
の製鉄原料の焼結法に関する。
(従来の技術)
製鉄用の鉄鉱石のうち粉状鉄鉱石は焼結により
塊成化してから高炉に装入されている。
一般に、このような粉状鉱石などの製鉄原料
(以下、単に“原料”という)の塊成化法として
DL型(ドワイトロイド型)焼結機が用いられて
きた。これは第1図に示す如く、焼結ストランド
1の回りを周回回動せしめられる多数のパレツト
2上に、ホツパー3,4からそれぞれ床敷鉱、焼
結原料を順次供給し、点火炉5を通過する過程で
焼結原料表面に点火し、パレツト移動域下に配し
た風箱6からブロワー7て吸引することによつて
原料上方から下方に空気を流通させ、パレツトが
排鉱端に向う間に原料の焼結を上方から下方に向
けて進行させ、排鉱端直前にて焼成を完了して塊
成化した焼結鉱を得る方法である。
この間の焼結の進行状況は第2図に示す通り
で、符号8は原料を示し、斜線部分は焼結反応帯
9を、さらに焼結反応帯上に位置する符号10は
焼結完了帯をそれぞれ示している。原料には燃料
として粉コークスおよび高炉ガス灰等の固定炭素
含有材料が予め配合されており(主に粉コークス
を使用するので、以下粉コークスで代表させる)、
点火炉5で点火後、上方よりO2濃度21%の空気
を通気せしめて固定炭素を燃焼させ、これにより
鉱石の溶融焼結を行つている。燃焼排ガスは風箱
6を通して排気されるが、このときの排ガス中の
O2濃度は13%程度である。この酸素濃度レベル
のガスは未だ固定炭素を燃焼させるだけの酸化力
を保持しており、したがつて排ガスの再利用が望
まれる。
(発明が解決しようとする問題点)
したがつて、かかる排ガス再利用技術の一つと
して、従来より「鉄と鋼」Vol.69、No.4、72頁に
例示されるような、排ガスの焼結ストランドへの
循環技術が実施されている。これはストランド後
半の排ガスを抽気し、これを再度原料表面に吹き
付けて焼成ガスとして再利用を図るもので、大気
放散ガス量低減、窒素酸化物低減、さらに排熱回
収量増加等に効果がある。しかし、焼結層内で起
こる固定炭素の燃焼および焼結反応自体は、第2
図に示す従来の焼結法と同様であり、このため焼
結進行速度増加による生産性向上効果は達成でき
ない。
排ガスを再度焼結反応促進に利用し、かつ焼結
進行速度を速めるためには、原料層内で焼結反応
を同時多発的に進行させる必要がある。
これを具体的に実現した方法として特開昭47−
26304号に示される方法がある。この方法は、原
料供給装置および点火炉をパレツト進行方向に位
置をずらして複数個設け、供給された各々の原料
表面に順次点火せしめて、焼結反応を進行させる
もので、この操作により排ガスの再利用と焼結反
応速度の大幅な増加が可能となり、この結果、生
産性向上が達成できる。2段式の場合の焼結進行
状況を第3図に模式的に示す。図中、符号は第2
図のそれに同じである。上層を通過した排ガスは
再び下層で燃焼用に利用される。
しかしながら、この2段点火式焼結法では、焼
結過程において上層から下層に流入するガスは酸
素濃度が低く、このため下層に配合された粉コー
クスは不完全燃焼の状態に陥りやすく、燃焼発熱
量が減少することとなる。この結果、層内の温度
が低下し、十分な溶融焼結化が達成できず、成品
焼結鉱の強度劣化を惹起することとなり、これが
多段点火式焼結法の欠点となつている。
これに関連して、1段点火式の場合であるが、
コークス配合量を上層から下層に向かつて順次減
少するように傾斜的または段階的に変えることに
よつて、層の上下での熱量不均衡を小さくするこ
とが提案されている(特公昭59−31576号)。
かくして、本発明の目的とするところは、2段
式焼結法において下層に含有される固定炭素を効
率良く燃焼させる焼結方法を提供することであ
る。
(問題点を解決するための手段)
焼結鉱の成品強度は焼結反応温度によつて決
り、これを決定する主要因は燃料固定炭素量と層
高位置である。すなわち、粉コークスの増量によ
り燃焼発熱量が増加して反応温度を上昇させるこ
と、また層高下方に位置するほど焼結反応帯に流
入するガス温度が高くこれもまた反応温度を上昇
させることは良く知られた現象である。
そこで、従来の1段点火焼結法では、前述の特
公昭59−31576号に開示されているように、熱交
換によつて上反応帯に流入するガス温度が低くな
る上層部の強度低下防止を目的として粉コークス
を上層に多く、下層側に少なく配合して、反応温
度をより均一にしているのである。
しかし、この方法は装入した原料の1個所だけ
に点火する場合にのみ成立する技術で、原料層に
2ケ所から点火し焼結反応の同時進行を図る2段
点火式焼結法では、極端な下層強度低下を招くた
め高炉装入物としては不適の成品となる。この原
因は次のように考えられる。
すなわち、一般に、焼結層中の粉コークスの燃
焼は、含有される固定炭素分の通過ガス中の酸素
による酸化反応に起こるものであり、十分に酸素
が存在する場合は(1)式に示す完全燃焼の状態とな
り、発熱量は93.989kcal/酸素モルとなる。これ
に対し、酸素が不足すると、(2)式に示す不完全燃
焼の状態となり、この時の発熱量は52.796kcal/
酸素モルとなり、酸素1モルを基準にして考えれ
ば不完全燃焼時の発熱量は完全燃焼時のそれに比
べて44%減少する。
C+O2=CO2 ……(1)式
(発熱量=93.989kcal/酸素モル)
2C+O2=2CO2 ……(2)式
(発熱量=52.796kcal/酸素モル)
前述した2段焼結時の下層強度低下は、上層粉
コークスを燃焼した後の低O2濃度ガスで下層粉
コークスの燃焼反応が進行するため下層では不完
全燃焼になりやすく、溶融焼結に必要な熱量が確
保されにくいからである。上述の1段点火焼結法
と同様に上層の粉コークス配合を多くすると、こ
の操作が下層粉コークスの不完全燃焼状態をさら
に惹起し、下層強度の極端な低下を招くのであ
る。したがつて、2段焼結法では下層に配合する
粉コークスの燃焼性改善が肝要であるが、本発明
者らは検討の結果、酸素消費の観点からまず全層
にわたる粉コークス濃度に制限を設ける必要があ
り、さらにこの中で、従来の知見とは逆に上層に
粉コークスを少なく、下層に粉コークスを多くし
た傾斜的配合操作が適切な方法であることを見出
した。
かかる知見にもとずいて、2段焼結法において
上述のように全層における配合コークス量の制限
とともに上層と下層とで配合コークス量を変えて
操業を行なつたところ、十分な結合強度をもつた
焼結鉱が得られることを確認し、本発明を完成し
た。
よつて、本発明の要旨とするところは、製鉄原
料を焼結装置の床上に層高方向に2層に積荷する
と同時に各製鉄原料層表面に点火せしめ、各層の
焼結反応を同時多発的に進行させる2段点火式焼
結方法において、焼結しようとする製鉄原料中の
固定炭素濃度、例えば燃料粉コークス配合量に関
して、全層における濃度を一定濃度以下に制限す
ると共に、この濃度が上層側に少なく下層側に多
くなるように燃料源材料を配合することを特徴と
する、製鉄原料の焼結方法である。
ここに、「製鉄原料」とは、鉄鉱石の予備処理
段階で発生する粉鉱石および最初からその状態で
存在する粉鉱石、そして各種製鉄ダスト、スケー
ルなどを含み、これに粉石灰石などの造滓剤と返
鉱を加えたものである。製鉄業にあつていわゆる
焼結原料として良く知られているもので、その具
体的内容において特に制限されるものではない。
製鉄原料の焼結にあつては燃料として粉コーク
スおよび高炉ガス灰などの固定炭素含有材料が原
料中に配合されるが、本発明の方法においては、
酸素の必要量と供給量のバランスを確保するため
に、固定炭素含有材料の配合量に量的制限が加え
られる。すなわち、第5図に示されるごとく、全
層平均濃度で、原料中の粉コークス濃度は3.6wt
%以下、固定炭素(F.C.)濃度としては3.3wt%
以下とする。
この全層平均濃度の量的制限に加えて、本発明
にあつては、原料中F.C.濃度が上層で少なく、下
層で多くなるように、F.C.含有材料の配合量を層
ごとに変化させるのである。
したがつて、本発明によれば、吸引ガス中の
O2はほぼ全部が固定炭素燃焼に利用され、それ
により発生した熱も効率的に燃焼反応に利用でき
るため、下層の焼結鉱強度も上層のそれと比べて
ほとんど低下しない均一な特性の成品を得ること
ができ、また総合的に大幅なる強度改善を達成す
ることができるものである。
(作用)
次に、添付図面によつて本発明をさらに説明す
る。
まず、焼結鍋装置について説明すると、第4図
は本発明を実施するための焼結鍋を一部断面で示
すものである。図中、符号11は本体を示し、こ
れは高さ600mm内径300mmの円筒状になつており、
底部には間隔をおいた格子よりなるグレート12
が設けられ、その下部に風箱13があり、排風機
(図面省略)により吸引するようになつている。
点火は鍋本体状に設置したコークス炉ガス燃焼バ
ーナー14により行う。この試験鍋を用い、グレ
ート12状に床敷鉱15を敷きその上に所定の原
料16を2段に装入し、この充填原料表面上に各
段装入ごとに着火して焼成を行なつた。
次に焼成試験時の操作を説明すると、最初に層
高300mm相当分の原料を装入して点火し、点火完
了直後さらにまた原料を層高300mm相当分装入し、
再度点火を行なつた後大気吸引で焼成した。原料
に配合する粉コークスおよび高炉ガス灰は予め設
定した量に調整して用いた。
実施例
本例では、第4図に示す装置を使い、2段式焼
結を行なつた。原料組成および焼結条件はそれぞ
れ第1表および第2表にまとめて示す。第1表
中、粉コークスの配合量は、粉コークス以外の原
料の合計を100%としたときの重量%である。
(Industrial Application Field) The present invention relates to a method for sintering raw materials for iron manufacturing, and particularly to a method for sintering raw materials for iron manufacturing using a two-stage ignition method. (Prior Art) Powdered iron ore, which is used for iron ore manufacturing, is agglomerated by sintering and then charged into a blast furnace. Generally, as a method for agglomerating ironmaking raw materials (hereinafter simply referred to as "raw materials") such as powdered ore,
A DL type (Dwight Lloyd type) sintering machine has been used. As shown in FIG. 1, bedding ore and sintering raw materials are sequentially supplied from hoppers 3 and 4 onto a large number of pallets 2 which are rotated around a sintered strand 1, and an ignition furnace 5 is started. During the process of passing, the surface of the sintered raw material is ignited, and air is circulated from above the raw material to below by suctioning it with a blower 7 from a wind box 6 placed below the pallet movement area, and as the pallet moves toward the discharge end. In this method, the raw material is sintered from the top to the bottom, and the sintering is completed just before the ore discharge end to obtain agglomerated sintered ore. The progress of sintering during this period is as shown in Figure 2, where numeral 8 indicates the raw material, the shaded area indicates the sintering reaction zone 9, and the numeral 10 located above the sintering reaction zone indicates the sintering completion zone. are shown respectively. The raw material is pre-blended with fixed carbon-containing materials such as coke powder and blast furnace gas ash as fuel (coke powder is mainly used, so it will be referred to as coke powder below).
After ignition in the ignition furnace 5, air with an O 2 concentration of 21% is vented from above to burn the fixed carbon, thereby melting and sintering the ore. The combustion exhaust gas is exhausted through the wind box 6, but the
The O2 concentration is around 13%. Gas at this oxygen concentration level still has enough oxidizing power to burn fixed carbon, and therefore it is desirable to reuse the exhaust gas. (Problems to be Solved by the Invention) Therefore, as one of the exhaust gas reuse technologies, the exhaust gas reuse technology as exemplified in "Tetsu to Hagane" Vol. 69, No. 4, p. 72 has been proposed. Circulation technology to sintered strands is implemented. This extracts the exhaust gas from the latter half of the strand and sprays it onto the surface of the raw material again to reuse it as firing gas, which is effective in reducing the amount of gas released into the atmosphere, reducing nitrogen oxides, and increasing the amount of waste heat recovered. . However, the combustion of fixed carbon and the sintering reaction itself that occur within the sintered layer are secondary to
This is similar to the conventional sintering method shown in the figure, and therefore the productivity improvement effect by increasing the sintering progress rate cannot be achieved. In order to use the exhaust gas again to promote the sintering reaction and to speed up the sintering progress, it is necessary to allow the sintering reaction to proceed simultaneously in the raw material layer. As a concrete method for realizing this, JP-A-47-
There is a method shown in No. 26304. In this method, a plurality of raw material supply devices and ignition furnaces are provided at different positions in the pallet advancing direction, and the surfaces of each supplied raw material are ignited in sequence to advance the sintering reaction. Reuse and sintering reaction rates can be significantly increased, resulting in improved productivity. The progress of sintering in the case of the two-stage method is schematically shown in FIG. In the figure, the symbol is the second
It is the same as that in the figure. The exhaust gas that has passed through the upper layer is used again for combustion in the lower layer. However, in this two-stage ignition sintering method, the gas flowing from the upper layer to the lower layer during the sintering process has a low oxygen concentration, so the coke breeze blended in the lower layer tends to be incompletely combusted, causing combustion heat generation. The amount will decrease. As a result, the temperature within the layer decreases, making it impossible to achieve sufficient melting and sintering, leading to deterioration in the strength of the finished sintered ore, which is a drawback of the multi-stage ignition sintering method. In this regard, in the case of a single-stage ignition type,
It has been proposed to reduce the heat disparity between the upper and lower layers by changing the coke content gradually or stepwise so that it decreases from the upper layer to the lower layer (Japanese Patent Publication No. 59-31576). issue). Thus, an object of the present invention is to provide a sintering method that efficiently burns the fixed carbon contained in the lower layer in a two-stage sintering method. (Means for solving the problem) The strength of the sintered ore product is determined by the sintering reaction temperature, and the main factors determining this are the amount of fuel fixed carbon and the bed height position. In other words, increasing the amount of coke breeze increases the combustion calorific value and raises the reaction temperature, and the lower the bed height is, the higher the temperature of the gas flowing into the sintering reaction zone, which also increases the reaction temperature. This is a well-known phenomenon. Therefore, in the conventional one-stage ignition sintering method, as disclosed in the above-mentioned Japanese Patent Publication No. 59-31576, the temperature of the gas flowing into the upper reaction zone is lowered by heat exchange, which prevents the strength from decreasing in the upper layer. For this purpose, more coke powder is mixed in the upper layer and less in the lower layer to make the reaction temperature more uniform. However, this method only works when igniting the charged raw material at only one location, and the two-stage ignition sintering method, in which the raw material layer is ignited at two locations to allow the sintering reaction to proceed simultaneously, is extremely difficult to achieve. This results in a decrease in the strength of the lower layer, making the product unsuitable for use as a blast furnace charge. The reason for this is thought to be as follows. That is, in general, the combustion of coke breeze in the sintered layer occurs due to the oxidation reaction of the fixed carbon contained therein due to oxygen in the passing gas. Complete combustion occurs, and the calorific value is 93.989kcal/mole of oxygen. On the other hand, when oxygen is insufficient, incomplete combustion occurs as shown in equation (2), and the calorific value at this time is 52.796kcal/
Based on 1 mole of oxygen, the amount of heat generated during incomplete combustion is 44% lower than that during complete combustion. C + O 2 = CO 2 ... Equation (1) (Calorific value = 93.989 kcal / oxygen mole) 2C + O 2 = 2CO 2 ... (2) Equation (calorific value = 52.796 kcal / oxygen mole) During the two-stage sintering described above The lower layer strength decreases because the combustion reaction of the lower layer coke powder proceeds with the low O 2 concentration gas after burning the upper layer coke powder, which tends to cause incomplete combustion in the lower layer, making it difficult to secure the amount of heat required for melting and sintering. It is. Similar to the above-mentioned one-stage ignition sintering method, if the blend of coke breeze in the upper layer is increased, this operation further induces incomplete combustion of the coke breeze in the lower layer, leading to an extreme decrease in the strength of the lower layer. Therefore, in the two-stage sintering method, it is important to improve the combustibility of the coke breeze blended in the lower layer, but as a result of our studies, the present inventors first decided to limit the coke breeze concentration throughout the entire layer from the viewpoint of oxygen consumption. Furthermore, contrary to conventional knowledge, it was discovered that a gradient blending operation in which the upper layer contains less coke breeze and the lower layer contains more coke breeze is an appropriate method. Based on this knowledge, we operated the two-stage sintering method by limiting the amount of coke blended in all layers as described above and by changing the amount of coke blended in the upper and lower layers. It was confirmed that motsuta sintered ore could be obtained, and the present invention was completed. Therefore, the gist of the present invention is to load steelmaking raw materials in two layers in the layer height direction on the floor of a sintering device, simultaneously ignite the surface of each steelmaking raw material layer, and simultaneously and multiple times cause a sintering reaction in each layer. In the two-stage ignition type sintering method, the fixed carbon concentration in the steelmaking raw material to be sintered, for example, the amount of fuel coke mixed, is limited to a certain concentration or less in all layers, and this concentration is This is a method for sintering raw materials for iron making, which is characterized by blending fuel source materials so that they are less in the upper layer and more in the lower layer. Here, "steelmaking raw materials" include powdered ore generated during the pre-processing stage of iron ore, powdered ore existing in that state from the beginning, various ironmaking dust, scale, etc., and slag such as powdered limestone. This is the result of adding minerals and return minerals. It is well known as a so-called sintering raw material in the steel industry, and its specific content is not particularly limited. When sintering raw materials for steelmaking, fixed carbon-containing materials such as coke breeze and blast furnace gas ash are blended into the raw materials as fuel, but in the method of the present invention,
In order to ensure a balance between the required amount of oxygen and the supplied amount, a quantitative limit is placed on the amount of fixed carbon-containing material incorporated. In other words, as shown in Figure 5, the average concentration of coke powder in the raw material is 3.6wt.
% or less, fixed carbon (FC) concentration is 3.3wt%
The following shall apply. In addition to this quantitative restriction on the average concentration of all layers, in the present invention, the blending amount of the FC-containing material is varied for each layer so that the FC concentration in the raw material is lower in the upper layer and higher in the lower layer. . Therefore, according to the present invention, in the suction gas,
Almost all of the O 2 is used for fixed carbon combustion, and the heat generated can also be efficiently used for combustion reactions, making it possible to produce products with uniform properties in which the strength of the sintered ore in the lower layer hardly decreases compared to that in the upper layer. It is possible to achieve a significant improvement in overall strength. (Operation) Next, the present invention will be further explained with reference to the accompanying drawings. First, the sintering pot device will be described. FIG. 4 shows a partially sectional view of the sintering pot for carrying out the present invention. In the figure, numeral 11 indicates the main body, which has a cylindrical shape with a height of 600 mm and an inner diameter of 300 mm.
Grate 12 consisting of a grid at intervals on the bottom
A wind box 13 is provided at the bottom of the air box 13, and suction is performed by an exhaust fan (not shown).
Ignition is performed by a coke oven gas combustion burner 14 installed in the shape of the pot body. Using this test pot, bedding ore 15 is laid out in the shape of a grate 12, and predetermined raw materials 16 are charged thereon in two stages, and the surface of the filled raw materials is ignited and fired after each stage is charged. Ta. Next, to explain the operation during the firing test, first, raw materials equivalent to a bed height of 300 mm are charged and ignited, and immediately after the ignition is completed, raw materials are charged again for a bed height of 300 mm.
After igniting it again, it was fired by atmospheric suction. The coke powder and blast furnace gas ash to be mixed into the raw materials were adjusted to preset amounts before use. Example In this example, two-stage sintering was carried out using the apparatus shown in FIG. The raw material composition and sintering conditions are summarized in Tables 1 and 2, respectively. In Table 1, the blended amount of coke powder is % by weight when the total of raw materials other than coke powder is 100%.
【表】【table】
【表】
第5図に、本発明方法を実施した場合の効果を
比較例のそれとともにグラフにまとめて示す。
図中、●印は上・下層の粉コークスの配合率を
同一にした場合(比較例)の強度(JIS M8712に
開示されるTI値)を、△、▲印は下層の粉コー
クス配合率を上層のそれよりも多くした場合(本
発明法)、○印は逆に上層の粉コークス配合率を
下層のそれよりも多くした場合(比較例)の強度
結果を示す。なお、図中の破線は本発明法実施結
果を、実線は比較例実施結果を示す。
この場合、全層のコークス配合率が3.6wt%以
下(固定炭素濃度で3.3wt%以下)の条件内では、
粉コークス配合率の増加により強度が向上する。
これに対し、全層のコークス配合率が3.6wt%以
上(固定炭素濃度で3.3wt%以上)の条件では強
度が大幅に低下している。これは先に述べたよう
に、コークス配合率3.6%以下で固定炭素の燃焼
に必要なO2量は供給O2量よりも小さく、燃焼性
に関する問題はあるにしても酸素欠乏をきたすこ
とはないが、コークス配合率3.6%以上では必要
O2量の方が供給O2量よりも大きくなり酸素欠乏
を起こし、大幅な強度低下をきたすばかりでなく
最悪の場合には燃焼できなくなり焼結不能におち
いるためである。したがつて、2段点火焼結法を
行うためには、上層・下層のコークス配合率にか
かわらず全層平均において3.6%以上のコークス
配合率になると強度低下が発生する。
さて、全層のコークス配合率が3.6wt%以下の
場合、すなわち燃焼に必要なO2量が確保されて
いる場合においては、上層はO221%の大気で焼
成されるため粉コークス配合率の増加とともに強
度は改善されるが、当然のことながら上層の粉コ
ークス配合率の増加は下層の供給されるO2ガス
濃度の低下をまねき下層部での粉コークスの燃焼
性を悪化させ、結果的には上層の強度向上を図る
ものの下層の強度低下を招き、その改善効果は相
殺される。一方、下層での粉コークス配合率の増
加は、燃焼性の悪い状態ながらも燃料増から発熱
増となり強度向上をもたらすが、この場合下層部
から出る排ガスO2濃度が低くても他に影響を及
ぼさないので、結果的に強度改善につながる。
したがつて、2段点火焼結時には1段点火焼結
時とは全く異なり、全層にわたる粉コークス配合
率3.6%以下(固定炭素濃度3.3%以下)の制限を
設けるとともに、下層部のコークス配合率は上層
部のそれよりも多くすることが強度改善上好まし
く、逆に、上層・下層の粉コークス配合率を同一
にする操作、あるいは特公昭59−31576号で開示
される上層部に粉コークス配合率を高く、下層を
低くする操作は好ましくないと言える。
さらに本発明の別の適用例として、上層と下層
の粉コークス配合率を同一として下層のみに固定
炭素を含む高炉ガス灰を添加した場合について述
べる。
原料配合率を第3表に示す。なお、焼成方法は
前述実施例と同様の方法をとつた。その結果成品
強度TIは59%となり、第5図の結果に比しても
良好なものと評価できる。第3表中、粉コークス
の配合量は、粉コークス以外の原料の合計を100
%としたときの重量%である。
このように本発明においては、燃料となる固定
炭素濃度が全層平均で3.3wt%以下でかつ上層よ
りも下層に多くなるように操作すれば良く、その
銘柄は粉コークスにこだわるものではなく、高炉
ガス灰の他石灰などであつてもよい。[Table] FIG. 5 shows the effects of implementing the method of the present invention in a graph together with those of comparative examples. In the figure, the ● mark indicates the strength (TI value disclosed in JIS M8712) when the blending ratio of coke breeze in the upper and lower layers is the same (comparative example), and the △ and ▲ marks indicate the blending ratio of coke breeze in the lower layer. On the other hand, the circles indicate the strength results when the coke powder blending ratio in the upper layer was higher than that in the lower layer (comparative example). In addition, the broken line in the figure shows the result of implementing the method of the present invention, and the solid line shows the result of implementing the comparative example. In this case, under the condition that the coke content ratio in all layers is 3.6wt% or less (fixed carbon concentration is 3.3wt% or less),
Strength is improved by increasing the coke powder blending ratio.
On the other hand, when the coke content in all layers is 3.6wt% or more (fixed carbon concentration is 3.3wt% or more), the strength is significantly reduced. As mentioned earlier, the amount of O 2 required for combustion of fixed carbon is smaller than the amount of supplied O 2 when the coke blending ratio is 3.6% or less, and although there are problems with combustibility, oxygen deficiency will not occur. Not required, but necessary if coke content is 3.6% or higher
This is because the amount of O 2 becomes larger than the amount of O 2 supplied, causing oxygen deficiency, which not only causes a significant decrease in strength, but also, in the worst case, makes it impossible to burn and sintering becomes impossible. Therefore, in order to carry out the two-stage ignition sintering method, strength decreases when the coke content is 3.6% or more on average for all layers, regardless of the coke content in the upper and lower layers. Now, when the coke blending ratio in all layers is 3.6wt% or less, that is, when the amount of O 2 necessary for combustion is secured, the upper layer is fired in an atmosphere with 21% O 2 , so the coke powder blending ratio is lower than 3.6wt%. The strength improves with an increase in coke breeze, but as a matter of course, an increase in the coke breeze blending ratio in the upper layer leads to a decrease in the O 2 gas concentration supplied to the lower layer, which worsens the combustibility of the coke breeze in the lower layer. In other words, although the strength of the upper layer is improved, the strength of the lower layer is reduced, and the improvement effect is canceled out. On the other hand, an increase in the blending ratio of coke breeze in the lower layer results in increased heat generation due to the increase in fuel, even though the combustibility is poor , resulting in an increase in strength. As a result, the strength is improved. Therefore, during two-stage ignition sintering, which is completely different from one-stage ignition sintering, there is a limit to the coke powder blending ratio of 3.6% or less (fixed carbon concentration of 3.3% or less) throughout the entire layer, and the coke blending ratio in the lower layer is In order to improve the strength, it is preferable to make the coke ratio higher than that of the upper layer.Conversely, it is preferable to make the coke powder mixture ratio of the upper layer and the lower layer the same, or to add coke powder to the upper layer as disclosed in Japanese Patent Publication No. 59-31576. It can be said that it is not preferable to increase the blending ratio and lower the lower layer. Furthermore, as another application example of the present invention, a case will be described in which the coke powder blending ratio in the upper layer and the lower layer is the same and blast furnace gas ash containing fixed carbon is added only to the lower layer. The raw material blending ratio is shown in Table 3. The firing method was the same as in the previous example. As a result, the product strength TI was 59%, which can be evaluated as being good compared to the results shown in FIG. In Table 3, the blended amount of coke powder is the total amount of raw materials other than coke powder.
% by weight. In this way, in the present invention, it is only necessary to operate so that the concentration of fixed carbon used as fuel is 3.3wt% or less on average in all layers and is higher in the lower layer than in the upper layer, and the brand is not limited to coke breeze. In addition to blast furnace gas ash, lime may also be used.
第1図は、従来のDL型焼結機の略式説明図;
第2図は1段焼結法における焼結進行状況を示す
グラフ;第3図は、多段焼結法における第2図と
同様のグラフ;第4図は、本発明において利用す
る焼結機のバケツトの断面図;および第5図は、
上下層における粉コークス配合率の差および全層
平均における粉コークス配合率とTIとの関係を
示すグラフである。
1:焼結ストランド、2:パレツト、3,4:
ホツパー、5:点火炉、6:風箱、7:ブロワ
ー、8:原料帯、9:反応帯、10:焼結完了
帯、11:焼結鍋、12:グレート、13:風
箱、14:バーナー、15:床敷鉱、16:原
料。
Figure 1 is a schematic illustration of a conventional DL type sintering machine;
Figure 2 is a graph showing the sintering progress in the one-stage sintering method; Figure 3 is a graph similar to Figure 2 in the multi-stage sintering method; Figure 4 is the graph of the sintering machine used in the present invention. A cross-sectional view of the bucket; and FIG.
FIG. 2 is a graph showing the difference in the coke powder blending ratio between the upper and lower layers and the relationship between the coke powder blending ratio and TI in the average of all layers. 1: Sintered strand, 2: Pallet, 3, 4:
Hopper, 5: Ignition furnace, 6: Wind box, 7: Blower, 8: Raw material zone, 9: Reaction zone, 10: Sintering completion zone, 11: Sintering pot, 12: Grate, 13: Wind box, 14: Burner, 15: Bed ore, 16: Raw material.
Claims (1)
に積荷すると同時に各製鉄原料層表面に点火せし
め、各層の焼結反応を同時多発的に進行させる2
段点火式焼結方法において、焼結しようとする製
鉄原料中の固定炭素濃度を全層平均で3.3wt%以
下とすると共に、原料中の固定炭素濃度が上層側
に少なく下層側に多くなるように固定炭素含有材
料を配合することを特徴とする、製鉄原料の焼結
方法。 2 固定炭素含有材料として粉コークスを用い、
全層平均で粉コークス配合量を3.6wt%以下とす
る、特許請求の範囲第1項記載の焼結方法。[Scope of Claims] 1. Iron-making raw materials are loaded in two layers in the layer height direction on the floor of a sintering device, and at the same time, the surface of each iron-making raw material layer is ignited, so that the sintering reaction of each layer proceeds simultaneously and multiple times. 2.
In the staged ignition sintering method, the fixed carbon concentration in the steel raw material to be sintered is set to 3.3wt% or less on average for all layers, and the fixed carbon concentration in the raw material is lower in the upper layer and higher in the lower layer. A method for sintering raw materials for iron making, characterized by blending a fixed carbon-containing material into a material containing fixed carbon. 2 Using coke powder as a fixed carbon-containing material,
The sintering method according to claim 1, wherein the average amount of coke powder mixed in all layers is 3.6 wt% or less.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP19906485A JPS6260829A (en) | 1985-09-09 | 1985-09-09 | Two-stage-ignition sintering method for raw material for iron manufacture |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP19906485A JPS6260829A (en) | 1985-09-09 | 1985-09-09 | Two-stage-ignition sintering method for raw material for iron manufacture |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6260829A JPS6260829A (en) | 1987-03-17 |
| JPH0567686B2 true JPH0567686B2 (en) | 1993-09-27 |
Family
ID=16401507
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP19906485A Granted JPS6260829A (en) | 1985-09-09 | 1985-09-09 | Two-stage-ignition sintering method for raw material for iron manufacture |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6260829A (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62107032A (en) * | 1985-11-01 | 1987-05-18 | Sumitomo Metal Ind Ltd | Two-stage ignition sintering method |
| CN112410544B (en) * | 2020-01-19 | 2023-03-10 | 中冶长天国际工程有限责任公司 | Double-layer sintering method |
| JP7381876B2 (en) * | 2020-01-31 | 2023-11-16 | 日本製鉄株式会社 | Sintered ore manufacturing method and sintering machine |
| JP7606083B2 (en) * | 2020-02-21 | 2024-12-25 | 日本製鉄株式会社 | Sinter manufacturing method |
-
1985
- 1985-09-09 JP JP19906485A patent/JPS6260829A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6260829A (en) | 1987-03-17 |
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