JP2008111172A - Method for operating blast furnace - Google Patents
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- JP2008111172A JP2008111172A JP2006295911A JP2006295911A JP2008111172A JP 2008111172 A JP2008111172 A JP 2008111172A JP 2006295911 A JP2006295911 A JP 2006295911A JP 2006295911 A JP2006295911 A JP 2006295911A JP 2008111172 A JP2008111172 A JP 2008111172A
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Abstract
Description
本発明は、石炭と鉄鉱石との混合物を成型して乾留して製造するフェロコークスを、高炉原料として使用する高炉の操業方法に関する。 The present invention relates to a method for operating a blast furnace using ferro-coke, which is produced by molding and dry distillation a mixture of coal and iron ore, as a blast furnace raw material.
高炉の還元材比低下のためには、フェロコークスを用いた、高炉の熱保存帯温度低下効果を利用する手法が有効である(例えば、特許文献1参照。)。石炭と鉄鉱石とを混合して成型した成型物を乾留して製造されるフェロコークスは、高反応性のため焼結鉱の還元を促進するとともに、一部還元された鉄鉱石が含まれているので高炉の熱保存帯温度を下げることができ、還元材比を低下させることができる。 In order to lower the reducing material ratio of the blast furnace, a technique using the effect of lowering the temperature of the thermal preservation zone of the blast furnace using ferro-coke is effective (for example, see Patent Document 1). Ferro-coke produced by dry distillation of a molded product formed by mixing coal and iron ore promotes reduction of sintered ore due to its high reactivity and contains partially reduced iron ore. Therefore, the temperature of the heat storage zone of the blast furnace can be lowered, and the reducing material ratio can be lowered.
しかし一方で、熱保存帯温度は、還元材比に影響を及ぼす他に、炉頂ガス温度にも影響を及ぼす。炉頂ガス温度が低下すると、炉頂での結露の発生や、ダスト付着によるダスト排出不良などの問題が発生する可能性がある。 However, on the other hand, the heat storage zone temperature affects not only the reducing material ratio but also the furnace top gas temperature. When the furnace top gas temperature decreases, problems such as the occurrence of condensation at the furnace top and defective dust discharge due to dust adhesion may occur.
図1〜図4を用いて、炉頂ガス温度が低下するメカニズムを説明する。 The mechanism by which the furnace top gas temperature decreases will be described with reference to FIGS.
高炉上部の高さ方向の温度分布は、熱流比(装入物とガスの熱容量比)を用いて記述される(例えば、非特許文献1参照。)。高炉内の温度分布の代表例を図1に示す。図1は高炉1の縦断面の概略図とその断面における温度分布を示すグラフであり、炉上部では一般に熱流比は1未満であり、一方、炉下部では吸熱反応が進行するため装入物熱容量が見掛け上大きくなって、熱流比は1を超える。両者の中間に熱流比がほぼ1になる領域2ができ、これが熱保存帯に相当する。
The temperature distribution in the height direction of the upper part of the blast furnace is described using a heat flow ratio (a heat capacity ratio between a charge and a gas) (for example, see Non-Patent Document 1). A typical example of the temperature distribution in the blast furnace is shown in FIG. FIG. 1 is a schematic diagram of a longitudinal section of a
炉上部装入物(固体)とガスの熱交換では、ガス側の入口温度は熱保存帯ガス温度、固体側の入口温度は装入時の装入物温度に相当し、熱流比が同一でも、両者の値によって高さ方向の温度分布、およびガス出口温度(炉頂ガス温度に相当)が変化する。熱保存帯温度と熱流比を変化させた場合の、固体温度とガス温度の計算例を図2に示す。縦軸の高さは、高炉における高さ位置を示し、炉頂部の高さを0mとして、炉頂部から下向きの長さで示している。図2(a)は熱保存帯温度950℃、熱流比0.864の場合であり、炉頂ガス温度は151℃である。図2(b)は熱保存帯温度750℃、熱流比0.864の場合であり、炉頂ガス温度は124℃である。図2(c)は熱保存帯温度750℃、熱流比0.915の場合であり、炉頂ガス温度は88℃である。同一の熱流比であっても、熱保存帯温度(炉上部熱交換のガス入口温度に相当)が低下すれば、炉頂ガス温度が低下し、還元材比低減による熱流比上昇が加われば、炉頂温度はさらに低下することが分かる。 In the heat exchange between the furnace top charge (solid) and gas, the gas side inlet temperature corresponds to the temperature of the heat storage zone gas, the solid side inlet temperature corresponds to the charge temperature at the time of charging, and the heat flow ratio is the same. The temperature distribution in the height direction and the gas outlet temperature (corresponding to the furnace top gas temperature) vary depending on both values. FIG. 2 shows a calculation example of the solid temperature and the gas temperature when the heat preservation zone temperature and the heat flow ratio are changed. The height of the vertical axis indicates the height position in the blast furnace, and the height at the top of the furnace is assumed to be 0 m, and the height is indicated by the downward length from the top of the furnace. FIG. 2A shows a case where the heat storage zone temperature is 950 ° C. and the heat flow ratio is 0.864, and the furnace top gas temperature is 151 ° C. FIG. 2B shows a case where the heat storage zone temperature is 750 ° C. and the heat flow ratio is 0.864, and the furnace top gas temperature is 124 ° C. FIG. 2C shows a case where the heat storage zone temperature is 750 ° C. and the heat flow ratio is 0.915, and the furnace top gas temperature is 88 ° C. Even if the heat flow ratio is the same, if the heat preservation zone temperature (corresponding to the gas inlet temperature of the furnace top heat exchange) decreases, the furnace top gas temperature decreases, and if the heat flow ratio increases due to the reduction of the reducing material ratio, It can be seen that the furnace top temperature further decreases.
図3は、リスト線図に基づく熱・物質収支モデル(以下、「リストモデル」と記載する。)から導出された、シャフト効率一定で熱保存帯温度をベース条件から100℃低下させた場合の炉頂ガス温度の変化の予測結果を示すグラフである。この計算では熱保存帯温度低下によりコークス比が27kg/t低下、熱流比が0.015上昇し、結果として炉頂ガス温度が58℃低下した。炉頂ガス温度58℃低下の内、24℃の低下分は熱流比上昇による影響であり(熱保存帯温度一定で熱流比のみを0.015上昇させた計算による)、残りの34℃が熱保存帯温度低下の影響である。 FIG. 3 shows a case where the heat storage zone temperature is lowered by 100 ° C. from the base condition with a constant shaft efficiency derived from a heat / mass balance model (hereinafter referred to as “list model”) based on the list diagram. It is a graph which shows the prediction result of the change of furnace top gas temperature. In this calculation, the coke ratio decreased by 27 kg / t and the heat flow ratio increased by 0.015 due to a decrease in the temperature of the heat preservation zone, and as a result, the furnace top gas temperature decreased by 58 ° C. Of the furnace gas temperature decrease of 58 ° C, the decrease of 24 ° C is due to the increase in the heat flow ratio (calculated by increasing the heat flow ratio by 0.015 with a constant heat storage zone temperature). This is the effect of a decrease in storage zone temperature.
図4にリストモデルにより計算した熱保存帯温度低下、シャフト効率増加、送風温度上昇により還元材比低減を指向した際のベース条件からの炉頂ガス温度の変化を示す。熱保存帯温度低下による低還元材比操業を指向する場合、シャフト効率増加や送風温度上昇といった手段に比べ同一熱流比において炉頂温度の低下幅が大きい。これは、前述のように熱流比上昇に加えて炉上部のガス−固体の熱交換におけるガス側の入口温度が低下するためである。 FIG. 4 shows changes in the furnace top gas temperature from the base condition when the reduction of the reducing material ratio is aimed at by reducing the temperature of the heat preservation zone, increasing the shaft efficiency, and increasing the blowing temperature calculated by the list model. When aiming at low-reducing-material ratio operation by lowering the temperature of the heat preservation zone, the furnace top temperature is greatly reduced at the same heat flow ratio as compared with means such as increasing shaft efficiency and raising the blowing temperature. This is because the inlet temperature on the gas side in the gas-solid heat exchange in the upper part of the furnace is lowered in addition to the increase in the heat flow ratio as described above.
一方、炉頂ガス温度が低下すると、排出ダスト量の減少を介して通気性の悪化等が発生することから、操業上炉頂ガス温度には下限値を設けている。特に炉頂ガス温度が100℃を下回る状態が継続すると、ダスト排出量の減少に加え、炉口部が水分凝集雰囲気となることにより高炉排ガスの一次除塵器として用いられているダストキャッチャーでの灰出し作業が困難となる他、炉口耐火物の損傷が問題になる(例えば、非特許文献2参照。)。 On the other hand, when the furnace top gas temperature is lowered, deterioration of air permeability occurs due to a decrease in the amount of discharged dust, and therefore, a lower limit is set for the furnace top gas temperature in operation. In particular, if the furnace top gas temperature continues below 100 ° C, in addition to the reduction in dust emissions, the ash in the dust catcher used as the primary dust remover for the blast furnace exhaust gas is created by the atmosphere at the furnace port becoming a moisture coagulation atmosphere. In addition to the difficulty of taking out, the damage of the furnace refractory becomes a problem (for example, refer nonpatent literature 2).
前述のように熱保存帯温度低下による低還元材比操業を指向する場合、シャフト効率向上等の操作に比べ、同一の熱流比上昇に対する炉頂温度低下量が大きく、従来以上に炉頂温度管理に留意する必要がある。従来、熱流比は炉頂ガス温度とほぼ対応する指標と捉えられており、熱流比をパラメータとした操業設計が実施されてきた。しかし、熱保存帯温度操作を行う場合は図4に示したように両者の関係が通常の関係からシフトするため、従来の熱流比の考え方では不十分である。
通常の高炉操業では、炉頂温度の低下による問題の発生を防止するため、炉頂温度を100℃以上、好ましくは120℃以上に保持した操業を行なっている。しかし上記のように、高炉原料としてフェロコークスを使用して熱保存帯温度低下による低還元材比操業を指向する場合炉頂ガス温度が大きく低下し、従来の操業条件の調整だけでは、炉頂温度を維持できない怖れがあり操業の制約となるため問題である。 In normal blast furnace operation, in order to prevent the occurrence of problems due to a decrease in the furnace top temperature, the operation is performed with the furnace top temperature maintained at 100 ° C. or higher, preferably 120 ° C. or higher. However, as described above, when ferro-coke is used as the blast furnace raw material and the operation is directed to low reducing material ratio operation by lowering the temperature of the heat preservation zone, the gas temperature at the top of the furnace is greatly reduced. There is a fear that the temperature cannot be maintained, which is a problem because it becomes a restriction of operation.
したがって本発明の目的は、このような従来技術の課題を解決し、フェロコークスを原料として炉頂から装入する高炉操業を行なう際に、炉頂ガス温度の低下を抑制することのできる高炉操業方法を提供することにある。 Therefore, the object of the present invention is to solve such problems of the prior art, and to perform a blast furnace operation that can suppress a decrease in the gas temperature at the top of the furnace when performing blast furnace operation using ferro-coke as a raw material from the top of the furnace. It is to provide a method.
このような課題を解決するための本発明の特徴は以下の通りである。
(1)装入原料の一部としてフェロコークスを使用する高炉操業の際に、羽口からの送風の酸素富化率、羽口からの還元材吹込み量、羽口からの送風の窒素富化量の中から選ばれる1種または2種以上を制御することで、炉頂ガス温度を制御することを特徴とする高炉操業方法。
(2)酸素富化率と炉頂ガス温度との関係を求め、該関係を用いて酸素富化率を低下させて炉頂ガス温度を上昇させることを特徴とする(1)に記載の高炉操業方法。
(3)還元材吹込み量と炉頂ガス温度との関係を求め、該関係を用いて還元材吹込み量を増加させることで炉頂ガス温度を上昇させることを特徴とする(1)または(2)に記載の高炉操業方法。
(4)窒素富化量と炉頂ガス温度との関係を求め、該関係を用いて窒素富化量を増加させることで炉頂ガス温度を上昇させることを特徴とする(1)ないし(3)のいずれかに記載の高炉操業方法。
The features of the present invention for solving such problems are as follows.
(1) During blast furnace operation using ferro-coke as part of the charged raw material, the oxygen enrichment rate of the blowing air from the tuyere, the amount of reducing material blown from the tuyere, the nitrogen richness of the blowing air from the tuyere A method for operating a blast furnace, wherein the top gas temperature is controlled by controlling one or more selected from among the conversion amounts.
(2) The blast furnace according to (1), wherein a relationship between the oxygen enrichment rate and the furnace top gas temperature is obtained, and the oxygen enrichment rate is decreased using the relationship to raise the furnace top gas temperature. Operation method.
(3) The relationship between the reducing material blowing amount and the furnace top gas temperature is obtained, and the furnace top gas temperature is increased by increasing the reducing material blowing amount using the relationship (1) or The blast furnace operating method described in (2).
(4) The relationship between the nitrogen enrichment amount and the furnace top gas temperature is obtained, and the furnace top gas temperature is increased by increasing the nitrogen enrichment amount using the relationship (1) to (3 ) A blast furnace operating method described in any of the above.
本発明によれば、高炉原料としてフェロコークスを使用して熱保存帯温度を低下させても高炉の炉頂ガス温度の低下を防止することが可能であり、還元材比を低下させた操業を安定して行なうことができる。 According to the present invention, even if ferrocoke is used as a blast furnace raw material and the heat preservation zone temperature is lowered, it is possible to prevent the furnace gas temperature of the blast furnace from being lowered, and an operation with a reduced reducing material ratio is performed. It can be performed stably.
本発明者は、リストモデルを用いた熱・物質バランス解析により熱保存帯温度と各種操業条件が炉頂ガス温度に及ぼす影響を明らかにし、これらを連動管理する手法を明らかにすることで本発明を完成した。 The present inventor clarified the influence of the heat preservation zone temperature and various operating conditions on the furnace top gas temperature by heat / material balance analysis using a list model, and clarified a method for managing these in conjunction with each other. Was completed.
高炉操業のベース条件を還元材比490kg/t(微粉炭比100kg/t)、炉頂ガス温度140℃とし、酸素富化率2.4体積%とした。検討例として、酸素富化率を±2.4%、微粉炭比を±50kg/t変更した条件、および熱保存帯温度を±50℃、±100℃変更した条件の際の熱流比と炉頂ガス温度の関係を計算した。結果を図5に示す。酸素富化率や微粉炭吹き込み量変化時と、熱保存帯温度変化時では、熱流比と炉頂温度の関係が大きく異なることが明らかになった。このように、熱流比に基づく考えでは、熱保存帯温度変化時の炉頂ガス温度予測は不十分であることがわかる。以上を踏まえ、各種操業因子が炉頂温度に及ぼす影響を整理して表1に示す。 The base conditions for blast furnace operation were a reducing material ratio of 490 kg / t (pulverized coal ratio of 100 kg / t), a furnace top gas temperature of 140 ° C., and an oxygen enrichment ratio of 2.4 vol%. As an example of examination, the heat flow ratio and furnace when the oxygen enrichment rate is ± 2.4%, the pulverized coal ratio is changed by ± 50 kg / t, and the heat preservation zone temperature is changed by ± 50 ° C. and ± 100 ° C. The relationship of the top gas temperature was calculated. The results are shown in FIG. It has been clarified that the relationship between the heat flow ratio and the furnace top temperature is greatly different when the oxygen enrichment rate and the amount of pulverized coal injection are changed and when the temperature of the heat preservation zone is changed. Thus, it can be seen that the estimation based on the heat flow ratio is insufficient for predicting the furnace top gas temperature when the temperature of the heat preservation zone changes. Based on the above, Table 1 summarizes the effects of various operating factors on the furnace top temperature.
熱流比ではなく、上記の酸素富化率、微粉炭吹き込み量、天然ガス吹き込み量、窒素富化量の影響を考慮した操業設計を行うことにより、フェロコークスを使用して熱保存帯温度が低下した場合に目標とする炉頂ガス温度を確保する操業条件を設定できる。なお、上記の係数は、吹き込み還元材に関してはその組成により、送風条件に関してはベースの状態により若干変化する。上記は一例であり、その都度、ベース条件に応じて影響を精査すれば良い。 The heat storage zone temperature is reduced using ferro-coke by designing the operation in consideration of the oxygen enrichment rate, pulverized coal injection amount, natural gas injection amount, and nitrogen enrichment amount, not the heat flow ratio. In this case, it is possible to set operation conditions for ensuring the target furnace top gas temperature. The above coefficient varies slightly depending on the composition of the blown-in reducing material and on the base condition with respect to the blowing conditions. The above is an example, and the influence may be scrutinized according to the base condition each time.
以上のことから検討すると、熱保存帯温度が低下した場合に、目標とする炉頂ガス温度を確保するための操業条件としては、イ)酸素富化率、ロ)微粉炭吹き込み量、天然ガス吹き込み量等の還元材吹込み量、ハ)窒素富化量の3つを考えることができる。以下、これらの条件について詳しく説明する。 Considering the above, the operating conditions for ensuring the target furnace top gas temperature when the heat storage zone temperature decreases are as follows: a) oxygen enrichment rate, b) pulverized coal injection amount, natural gas Three types can be considered: reducing material blowing amount such as blowing amount, and c) nitrogen enrichment amount. Hereinafter, these conditions will be described in detail.
イ)酸素富化率:高炉羽口からの送風の際に、送風空気に酸素を加えて富化し、送風の酸素量を一定とする操業を行なえば、生産量一定で炉内通過ガス量を減少させることができる。従って、酸素富化率を低減することで、生産量(固体降下速度)一定で炉内通過ガス量が増加することにより熱流比が低下し、炉頂ガス温度が上昇する。操業条件に応じた酸素富化率と炉頂ガス温度との関係を求め、該関係を用いて酸素富化率を低下させて炉頂ガス温度を上昇させることができる。なお、酸素富化率は、送風空気に混合した酸素量の体積%で表すものとする。 B) Oxygen enrichment rate: When air is blown from the blast furnace tuyere, oxygen is added to the blown air to enrich it, and if the operation is performed to keep the amount of oxygen blown constant, the amount of gas passing through the furnace can be reduced with constant production. Can be reduced. Therefore, by reducing the oxygen enrichment rate, the heat flow ratio decreases and the furnace top gas temperature rises by increasing the amount of gas passing through the furnace at a constant production rate (solid descending rate). The relationship between the oxygen enrichment rate and the furnace top gas temperature according to the operating conditions can be determined, and the oxygen enrichment rate can be reduced using this relationship to raise the furnace top gas temperature. The oxygen enrichment rate is expressed by volume% of the amount of oxygen mixed in the blown air.
ロ)還元材吹込み量:羽口から熱風とともに微粉炭等の還元材を高炉内に吹き込むことによりコークス使用量を低減する操業が行なわれている。この還元材吹込み量を増やすことで、固体降下速度が減少することにより熱流比が低下し、炉頂ガス温度が上昇する。還元材としては、微粉炭の他に、天然ガス、廃プラスチック等を用いることができる。操業条件に応じた還元材吹込み量と炉頂ガス温度との関係を求め、該関係を用いて還元材吹込み量を増加させることで炉頂ガス温度を上昇させることができる。なお、還元材吹込み量は溶銑1tあたりの吹込み量(kg/t)で表すものとする。 B) Reducing material injection amount: Operation to reduce the amount of coke used by blowing reducing material such as pulverized coal into the blast furnace together with hot air from the tuyere. By increasing the amount of reducing material blown in, the solid flow rate decreases, the heat flow ratio decreases, and the furnace top gas temperature increases. In addition to pulverized coal, natural gas, waste plastic, etc. can be used as the reducing material. The relationship between the reducing material injection amount and the furnace top gas temperature corresponding to the operating conditions is obtained, and the furnace top gas temperature can be increased by increasing the reducing material injection amount using this relationship. In addition, the reducing material injection amount shall be represented by the injection amount (kg / t) per 1 ton of hot metal.
ハ)窒素富化量:高炉羽口からの送風に、窒素を富化する操業を行なうことができる。窒素の富化により送風酸素量が減少し、これにより生産量一定で炉内通過ガス量を増加させることができ、炉頂ガス温度が上昇する。操業条件に応じた窒素富化量と炉頂ガス温度との関係を求め、該関係を用いて窒素富化量を増加させることで炉頂ガス温度を上昇させることができる。なお、窒素富化量は溶銑1tあたりの標準状態における窒素ガス吹込み体積(Nm3/t)で表すものとする。 C) Nitrogen-enriched amount: Nitrogen-enriched operation can be performed on the air blown from the blast furnace tuyere. The amount of blown oxygen decreases due to the enrichment of nitrogen, whereby the amount of gas passing through the furnace can be increased with a constant production volume, and the furnace top gas temperature increases. The relationship between the nitrogen enrichment amount and the furnace top gas temperature according to the operating conditions is obtained, and the furnace top gas temperature can be increased by increasing the nitrogen enrichment amount using this relationship. Note that the nitrogen enrichment amount is represented by the nitrogen gas blowing volume (Nm 3 / t) in a standard state per 1 ton of hot metal.
上記イ)、ロ)、ハ)は、それぞれ単独に制御しても効果があるが、1種または2種以上を組み合わせて制御することで、より標準的な操業条件に近い条件で、安定した操業を行なうことが可能となるが、この際、微粉炭燃焼性や理論燃焼温度の変化には留意した操業設計が必要である。 The above a), b) and c) are effective even when controlled individually, but by controlling by combining one type or two or more types, it is stable under conditions closer to standard operating conditions. It is possible to operate, but at this time, it is necessary to design the operation in consideration of changes in pulverized coal combustibility and theoretical combustion temperature.
本発明で用いるフェロコークスは、石炭と鉄鉱石とを主成分とする原料を成型して製造した成型物を加熱して、成型物中の石炭を乾留して製造されたものである。なお、石炭と鉄鉱石とを主成分とするとは、フェロコークスの原料が主として石炭と鉄鉱石であることを意味するものであり、石炭と鉄鉱石とを70mass%以上含有する原料を用いてフェロコークスを製造するものであるが、通常は石炭と鉄鉱石とを80mass%以上含有する原料を使用する。石炭と鉄鉱石の他に成型のためのバインダー等を使用することができる。成型は冷間または熱間で行い、冷間で成型を行なう場合は、原料にバインダーを添加することが好ましい。 Ferro-coke used in the present invention is manufactured by heating a molded product produced by molding a raw material mainly composed of coal and iron ore, and dry-distilling the coal in the molded product. The main component of coal and iron ore means that the raw material of ferro-coke is mainly coal and iron ore. Ferro-coke is made of a raw material containing 70 mass% or more of coal and iron ore. Although coke is produced, a raw material containing 80 mass% or more of coal and iron ore is usually used. In addition to coal and iron ore, a binder for molding can be used. Molding is carried out cold or hot, and in the case of cold molding, it is preferable to add a binder to the raw material.
高炉装入原料の一部としてフェロコークスを使用する高炉操業としては、従来の高炉装入原料に加えて、あるいは代替して、フェロコークスを使用するものであり、通常は鉄原料、コークス、フェロコークスを高炉装入原料とするものである。鉄原料は焼結鉱、塊鉱石、ペレット等から構成される。フェロコークスの装入方法としては、例えば、フェロコークスを鉄原料と混合した「鉄原料+フェロコークス」層と、通常のコークス層とを高炉内に交互に装入することができる。高炉の炉頂部から、まずコークスを装入してコークス層を形成し、次に鉄鉱石とフェロコークスとの混合物を装入して、「鉄原料+フェロコークス」層を形成し、以下、コークス層と「鉄原料+フェロコークス」層とのサイクルを順次繰り返して高炉の原料装入を行うものである。 As a blast furnace operation using ferro-coke as a part of blast furnace charge, ferro-coke is used in addition to or instead of conventional blast furnace charge, and usually iron raw material, coke, ferro Coke is used as a raw material for blast furnace charging. The iron raw material is composed of sintered ore, lump ore, pellets and the like. As a ferro-coke charging method, for example, an “iron raw material + ferro-coke” layer in which ferro-coke is mixed with an iron raw material and a normal coke layer can be alternately charged into a blast furnace. From the top of the blast furnace, first, coke is charged to form a coke layer, and then a mixture of iron ore and ferro-coke is charged to form an “iron raw material + ferro-coke” layer. The blast furnace raw material charging is performed by sequentially repeating the cycle of the layer and the “iron raw material + ferrocoke” layer.
内容積5000m3の高炉において、フェロコークスを装入原料として用いない通常の操業である、コークス比390kg/t、微粉炭比100kg/tの操業条件をベースに、鉄:コークス=0.4:0.6の質量比のフェロコークスを使用した操業試験(Case1〜5)を行なった。
In a blast furnace having an internal volume of 5000 m 3 , iron: coke = 0.4: An operation test (
フェロコークスは、以下のようにして製造した。鉄鉱石と石炭との混合物(0.4:0.6の質量比率)にバインダーとしてアスファルトピッチと軟ピッチの混合物を5mass%添加して、ミキサーで攪拌して混合後、線圧5t/cm、成型温度25℃で冷間成型して6ccのブリケット成型物を製造した。鉄鉱石には粒径100ミクロン以下(−100ミクロン)のペレットフィードを用いた。石炭には最大平均反射率1.0%の石炭を用いた。石炭の粒度は、全量を粒径3mm以下(−3mm)に粉砕したものを用いた。このブリケットを専用の乾留炉であるシャフト炉で加熱して石炭を乾留し、フェロコークスを製造した。フェロコークスと鉄原料とを混合し、該混合物と塊コークスとを交互に炉内に装入して操業を行なった。 Ferro-coke was produced as follows. 5 mass% of a mixture of asphalt pitch and soft pitch is added as a binder to a mixture of iron ore and coal (mass ratio of 0.4: 0.6), and after stirring and mixing with a mixer, a linear pressure of 5 t / cm, Cold molding was performed at a molding temperature of 25 ° C. to produce a 6 cc briquette molding. A pellet feed having a particle size of 100 microns or less (-100 microns) was used for the iron ore. Coal having a maximum average reflectance of 1.0% was used as the coal. The particle size of the coal used was pulverized to a particle size of 3 mm or less (-3 mm). This briquette was heated in a shaft furnace, which is a dedicated carbonization furnace, and carbon was carbonized to produce ferro-coke. Ferro-coke and iron raw material were mixed, and the mixture and lump coke were alternately charged into the furnace for operation.
表2にベース条件およびCase1〜5の高炉操業結果を示す。熱保存帯温度は炉頂から装入した垂直ゾンデで測定した。
Table 2 shows the base conditions and blast furnace operation results of
Case1は送風条件、微粉炭吹き込み量をベース条件と同じとして、コークスと置換してフェロコークスを使用した場合である。炉頂ガス温度が82℃に低下し、ダスト排出量であるダスト原単位が低下し通気変動が生じるとともに、ダストキャッチャーからの灰出しの際に水分が多量に流れ出し、作業が困難になったため、同条件での操業の継続が困難であった。
これに対し、炉頂ガス温度を110℃に調整することを目的とし、フェロコークス使用と同時に酸素富化率を低減した操業(Case2)、フェロコークス使用と同時に微粉炭吹き込み量を増加した操業(Case3)、およびフェロコークス使用と同時に天然ガス(LNG)吹き込み量を増加した操業(Case4)を行なった。Case2〜4では、ダスト原単位(ダスト比)はベースに対し若干低下したものの、操業が安定し、コークス比を低減した操業の継続が可能であった。
On the other hand, for the purpose of adjusting the furnace top gas temperature to 110 ° C., the operation that reduced the oxygen enrichment rate simultaneously with the use of ferro-coke (Case 2), the operation that increased the amount of pulverized coal injection simultaneously with the use of ferro-coke ( Simultaneously with the use of Case 3) and ferro-coke, an operation (Case 4) with an increased amount of natural gas (LNG) was carried out. In
また、ベース条件よりもさらに炉頂ガス温度をあげるべく、酸素富化率低減と窒素富化を併用した操業(Case5)も行なった。Case5においてもコークス比を低減した操業の継続が可能であった。
In addition, in order to raise the furnace top gas temperature further than the base condition, an operation (Case 5) in which oxygen enrichment reduction and nitrogen enrichment were combined was performed. In
酸素富化率、窒素富化量、微粉炭および天然ガス吹き込み量は、それらの単独操作量が炉頂ガス温度に及ぼす影響を事前に把握し、実際のフェロコークス使用操業時に条件を変更した。Case2〜5の本発明例の操業においては、炉頂ガス温度を100℃以上に維持して、コークス比を低減した操業を安定して継続することが可能であることが分かった。 The oxygen enrichment rate, nitrogen enrichment amount, pulverized coal and natural gas injection amount were grasped in advance to determine the effect of these single operation amounts on the furnace top gas temperature, and the conditions were changed during actual ferro-coke operation. In the operations of Examples 2 to 5 of the present invention, it was found that the operation at a reduced coke ratio can be stably continued by maintaining the furnace top gas temperature at 100 ° C. or higher.
1 高炉
2 熱保存帯
3 塊状帯
4 融着帯
5 滴下帯
6 レースウェイ
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Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2010137748A1 (en) | 2009-05-29 | 2010-12-02 | Jfeスチール株式会社 | Blast furnace operation method |
JP2011137217A (en) * | 2009-12-02 | 2011-07-14 | Jfe Steel Corp | Method for operating blast furnace |
JP2011252200A (en) * | 2010-06-02 | 2011-12-15 | Jfe Steel Corp | Method for operating blast furnace |
WO2014088031A1 (en) * | 2012-12-07 | 2014-06-12 | 新日鉄住金エンジニアリング株式会社 | Method for operating blast furnace and method for producing molten pig iron |
JP2014132122A (en) * | 2012-12-07 | 2014-07-17 | Nippon Steel & Sumikin Engineering Co Ltd | Method for operating blast furnace and method for manufacturing molten iron |
JP2020079440A (en) * | 2018-11-14 | 2020-05-28 | 日本製鉄株式会社 | Blast furnace operation method |
WO2022264561A1 (en) * | 2021-06-18 | 2022-12-22 | Jfeスチール株式会社 | Oxygen blast furnace and oxygen blast furnace operation method |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5723011A (en) * | 1980-06-05 | 1982-02-06 | Centre Rech Metallurgique | Operation of blast furnace |
JPH02200711A (en) * | 1989-01-30 | 1990-08-09 | Nippon Steel Corp | Method for operating blast furnace |
JP2000144219A (en) * | 1998-08-28 | 2000-05-26 | Nkk Corp | Operation of blast furnace |
JP2001234213A (en) * | 2000-02-28 | 2001-08-28 | Nippon Steel Corp | Blast furnace operation method |
JP2006028594A (en) * | 2004-07-16 | 2006-02-02 | Jfe Steel Kk | Method for operating blast furnace |
JP2008111145A (en) * | 2006-10-30 | 2008-05-15 | Jfe Steel Kk | Method for suppressing reduction in temperature at top of blast furnace in use of ferrocoke |
-
2006
- 2006-10-31 JP JP2006295911A patent/JP4910640B2/en active Active
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5723011A (en) * | 1980-06-05 | 1982-02-06 | Centre Rech Metallurgique | Operation of blast furnace |
JPH02200711A (en) * | 1989-01-30 | 1990-08-09 | Nippon Steel Corp | Method for operating blast furnace |
JP2000144219A (en) * | 1998-08-28 | 2000-05-26 | Nkk Corp | Operation of blast furnace |
JP2001234213A (en) * | 2000-02-28 | 2001-08-28 | Nippon Steel Corp | Blast furnace operation method |
JP2006028594A (en) * | 2004-07-16 | 2006-02-02 | Jfe Steel Kk | Method for operating blast furnace |
JP2008111145A (en) * | 2006-10-30 | 2008-05-15 | Jfe Steel Kk | Method for suppressing reduction in temperature at top of blast furnace in use of ferrocoke |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2010137748A1 (en) | 2009-05-29 | 2010-12-02 | Jfeスチール株式会社 | Blast furnace operation method |
JP2011137217A (en) * | 2009-12-02 | 2011-07-14 | Jfe Steel Corp | Method for operating blast furnace |
JP2011252200A (en) * | 2010-06-02 | 2011-12-15 | Jfe Steel Corp | Method for operating blast furnace |
WO2014088031A1 (en) * | 2012-12-07 | 2014-06-12 | 新日鉄住金エンジニアリング株式会社 | Method for operating blast furnace and method for producing molten pig iron |
JP2014132108A (en) * | 2012-12-07 | 2014-07-17 | Nippon Steel & Sumikin Engineering Co Ltd | Method for operating blast furnace and method for manufacturing molten iron |
JP2014132122A (en) * | 2012-12-07 | 2014-07-17 | Nippon Steel & Sumikin Engineering Co Ltd | Method for operating blast furnace and method for manufacturing molten iron |
US9816151B2 (en) | 2012-12-07 | 2017-11-14 | Nippon Steel & Sumikin Engineering Co., Ltd. | Method for operating blast furnace and method for producing molten pig iron |
JP2020079440A (en) * | 2018-11-14 | 2020-05-28 | 日本製鉄株式会社 | Blast furnace operation method |
JP7167652B2 (en) | 2018-11-14 | 2022-11-09 | 日本製鉄株式会社 | Blast furnace operation method |
WO2022264561A1 (en) * | 2021-06-18 | 2022-12-22 | Jfeスチール株式会社 | Oxygen blast furnace and oxygen blast furnace operation method |
JP7276612B1 (en) * | 2021-06-18 | 2023-05-18 | Jfeスチール株式会社 | Oxygen blast furnace and method of operating oxygen blast furnace |
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