JPH0425327B2 - - Google Patents
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- JPH0425327B2 JPH0425327B2 JP29669386A JP29669386A JPH0425327B2 JP H0425327 B2 JPH0425327 B2 JP H0425327B2 JP 29669386 A JP29669386 A JP 29669386A JP 29669386 A JP29669386 A JP 29669386A JP H0425327 B2 JPH0425327 B2 JP H0425327B2
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- calcined
- ore
- sio
- agglomerate
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Description
〔発明の技術分野〕
この発明は、高炉用または直接還元鉄用原料と
して好適な焼成塊成鉱の製造方法に関するもので
ある。
〔従来技術とその問題点〕
高炉用原料または直接還元製鉄用原料として、
粉鉄鉱石をペレツト化して焼成した焼成塊成鉱が
知られており、使用が拡大されつつある。
この焼成塊成鉱は、通常、次のように製造され
ている。
すなわち、粒径約8mm以下の粉鉄鉱石に、生石
灰、消石灰、石灰石、ベントナイト、高炉水砕ス
ラグおよびドロマイト等のうちの少なくとも1つ
からなる媒溶剤を、焼成塊成鉱中のCaO/SiO2
の値が1.0〜2.5程度となるように添加し、ミキサ
ーで混合する。そして、得られた混合物をデイス
ク型の第1の造粒機に供給し、水を加えて、第1
の造粒機により混合物を造粒し、粒径が例えば約
3〜13mmの生ペレツトに成形する。次いで、得ら
れた生ペレツトをデイスク型の第2の造粒機に供
給し、2.5〜4.0wt%程度の粉コークスを添加し
て、第2の造粒機により生ペレツトを更に造粒
し、これによつて表面に粉コークスを被覆した生
ペレツトを調製する。
そして、このようにして得られた生ペレツトを
無端移動グレート式焼成炉内に装入して、装入さ
れた生ペレツトの層を焼成炉のグレート上に乗つ
て、焼成炉の乾燥帯、点火帯および焼成帯を順次
通過させる。乾燥帯においては、生ペレツトの層
に上方から温度150〜350℃の乾燥用ガスを吹込
み、生ペレツトを乾燥する。点火帯においては、
乾燥された生ペレツトの層に上方から高温燃焼ガ
スを吹込み、生ペレツトの表面の粉コークスを点
火する。燃焼帯においては、粉コークスの燃焼に
よつて生じた高温燃焼ガスを生ペレツト層を通つ
て下方に吸引して、生ペレツトを焼成温度まで加
熱する。生ペレツトは、焼成帯における加熱によ
つて、その表面に形成されたカルシウムフエライ
トおよびスラグの少なくとも1つにより結合され
た焼成ペレツトからなる、大きいブロツク状の塊
りの焼成塊成鉱に焼成される。
そして、このようにして得られた大きいブロツ
ク状の塊りの焼成塊成鉱を焼成炉の下流端から排
出し、クラツシヤーによつて破砕したのち、スク
リーンによつて篩分けて、粒径3mm未満の篩下げ
の焼成塊成鉱片を除去し、かくして、複数個の焼
成ペレツトが結合した塊状の形の最大粒径50mm程
度の焼成塊成鉱および単体の焼成ペレツトの形の
粒径3〜13mm程度の焼成塊成鉱が製造される。
以上のようにして製造された焼成塊成鉱は、主
として還元性に優れた微細なカルシウムフエライ
トおよび微細なヘマタイトが多く形成されている
ので、優れた還元性を有している。また、複数個
の焼成ペレツトが結合した塊状の形の場合のみな
らず、単体の焼成ペレツトの形の場合にも、不規
則な形状を有しているので、高炉内に装入したと
きに、高炉内の中心部に偏つて流れ込むことがな
く、且つ、焼成塊成鉱間に隙間が生ずるために、
還元ガスの円滑な通過を阻害することがない。さ
らに、移送中の衝撃等によつて崩壊があつても、
複数個の焼成ペレツトが結合した塊状の形の焼成
塊成鉱が単体の焼成ペレツトに分離するだけなの
で、支障なく使用することができる。
しかしながら、従来の焼成塊成鉱はSiO2を5.5
〜6.0wt%程度含有していたため、還元率が60〜
70%程度と低く、また還元粉化率が35〜45%程度
と高かつた。さらに、焼成塊成鉱がSiO2を5.5〜
6.0wt%程度含有していることから、高炉のスラ
グ比も例えば360Kg/トンと高く、燃料比(また
はコークス比)も例えば520Kg/トンと高くなる
難点があつた。
〔発明の目的〕
この発明は、上述の現状に鑑み、粉鉄鉱石に媒
溶剤を添加、混合した混合物を造粒して生ペレツ
トを成形し、得られた生ペレツトに粉コークスを
被覆し、前記生ペレツトを無端移動グレート式焼
成炉に装入して、焼成塊成鉱を連続的に製造する
に際して、焼成塊成鉱の還元率および還元粉化率
を向上させることを目的とするものである。
〔発明の概要〕
この発明は、粉鉄鉱石に媒溶剤を添加、混合し
た混合物をデイスク型の造粒機で造粒して生ペレ
ツトを成形し、得られた生ペレツトに粉コークス
を被覆し、前記生ペレツトを無端移動グレート式
焼成炉に装入して連続的に焼成し、かくして、焼
成塊成鉱を連続的に製造する、焼成塊成鉱の製造
方法において、
前記粉鉄鉱石として、前記焼成塊成鉱中の
SiO2が0.5〜5.0wt%となるように配合した粉鉄鉱
石を使用することに特徴を有するものである。
〔発明の構成〕
以下、この発明の焼成塊成鉱の製造方法につい
て詳述する。
本発明者等は、粉鉄鉱石に媒溶剤を添加、混合
した混合物を造粒して生ペレツトを成形し、得ら
れた生ペレツトに粉コークスを被覆し、前記生ペ
レツトを無端移動グレート式焼成炉に装入して、
焼成塊成鉱を連続的に製造するに際して、焼成塊
成鉱の還元率および還元粉化率を向上すべく、鋭
意研究を重ねた。
従来、焼成塊成鉱中にSiO2を5.0〜6.0wt%も含
有していたのは、生ペレツトの焼成時に、粉鉄鉱
石中のSiO2に媒溶剤中のCaOと共にスラグを形
成させて、粉鉄鉱石同志を結合させ、塊状化させ
るためには、焼成塊成鉱中のSiO2含有率が約
5.0wt%以上となるように、粉鉄鉱石中にSiO2が
含有されていることが必要であるとされていたか
らである。
しかし、研究を進めたところ、粉鉄鉱石の造粒
にドラム型の造粒機を用い、しかも、粉鉄鉱石に
媒溶剤のみならず粉コークスをも添加して、造粒
して得られた生ペレツトの場合ならばともかく、
粉鉄鉱石の造粒にデイスク型の造粒機を用い、し
かも、粉コークスは粉鉄鉱石の造粒後に表面に被
覆するようにし、粉鉄鉱石には媒溶剤のみを添加
して、造粒して得られた生ペレツトの場合には、
造粒性が良く、球形の良好な塊まりに成形されて
いるので、粉鉄鉱石中のSiO2含有量が少なくて
も、生ペレツトの焼成時に粉鉄鉱石中のSiO2に
媒溶剤中のCaOと共にスラグを形成させて、粉鉄
鉱石同志を結合させ、良好に塊状化させることが
できることが判つた。従つて、焼成塊成鉱の還元
率および還元粉化率を向上させることが可能とな
る。
そこで、SiO2含有量の異なる配合の粒径約8
mm以下の粉鉄鉱石の各々から調製した生ペレツト
を用い、SiO2含有量を変化させて焼成塊成鉱を
製造する実験を行なつた。そして、焼成塊成鉱中
のSiO2含有量と、還元率および還元粉化率並び
に成品歩留りおよび落下強度を調べた。
その結果、焼成塊成鉱中のSiO2含有量を0.5〜
5.0wt%とすれば、焼成塊成鉱の還元率および還
元粉化率を大幅に向上でき、しかも、成品歩留り
および落下強度を低下させることがないことが判
つた。
第1図は、得られた焼成塊成鉱中のSiO2含有
量と還元率との関係を示すグラフ、第2図は、同
じく、SiO2含有量と還元粉化率との関係を示す
グラフ、第3図は、同じく、SiO2含有量と落下
強度との関係を示すグラフ、第4図は、同じく、
SiO2含有量と成品歩留りとの関係を示すグラフ
である。
第1図に示されるように、焼成塊成鉱の還元率
は、焼成塊成鉱中のSiO2含有量が多くなるにつ
れて低下しているが、SiO2含有量が0.5〜5.0wt%
の範囲内では80%以上と高い。そして、SiO2含
有量が5.0wt%を超えると、還元率は80%を下廻
り急激に低下する。焼成塊成鉱の還元粉化率は、
第2図に示されるように、焼成塊成鉱中のSiO2
含有量が0.5〜5.0wt%の範囲内では30%以下にな
つているが、SiO2含有量が5.0wt%を超えると還
元粉化率は30%を上廻る。
一方、焼成塊成鉱の落下強度は、第3図に示さ
れるように、焼成塊成鉱中のSiO2含有量が多く
なるにつれて増加しているが、SiO2含有量が0.5
〜5.0wt%の範囲内でも落下強度は約85%以上あ
つて、充分に維持されている。焼成塊成鉱の成品
歩留りは、第4図に示されるように、焼成塊成鉱
中のSiO2含有量が多くなるにつれて増加してい
るが、SiO2含有量が0.5〜5.0wt%の範囲内でも成
品歩留りは約75%以上あつて、充分に維持されて
いる。
なお、以上で、焼成塊成鉱中のSiO2含有量の
下限を0.5wt%までとしたのは、SiO2含有量が
0.5wt%未満の焼成塊成鉱を得ることは、粉鉄鉱
石の品位の点から殆ど困難であり、0.5wt%未満
は実用上意味がないからである。
従つて、焼成塊成鉱の成品歩留りおよび落下強
度を低下させずに、焼成塊成鉱の還元率を80%以
上、還元粉化率を30%以下とするためには、焼成
に使用する粉鉄鉱石として、焼成塊成鉱中の
SiO2含有量が0.5〜5.0wt%となるように配合した
粉鉄鉱石を用いるべきである。
この発明においては、以上のように、焼成に使
用する粉鉄鉱石として、焼成塊成鉱中のSiO2含
有量が0.5〜5.0wt%となるように配合した粉鉄鉱
石を使用して、焼成塊成鉱の還元率および還元粉
化率を大幅に向上させるものである。
この発明において、生ペレツトに被覆する粉コ
ークスの量は、従来と同様2.5〜4.0wt%とするの
が好ましい。これは、被覆する粉コークスの量が
2.5wt%未満では、焼成炉における生ペレツトの
焼成効率を高めることができず、生ペレツトを短
時間で高強度の焼成塊成鉱に焼成できないからで
あり、被覆する粉コークスの量が4.0wt%を超え
ると、焼成時の生ペレツトの温度が高くなり過ぎ
て、焼成塊成鉱の組織が緻密で気孔の少ないもの
となると同時に、被還元性の悪い溶融型組織、す
なわち、2次ヘマタイトや短冊型カルシウムフエ
ライトの多い組織となるためである。
この発明において、使用する粉鉄鉱石の粒径
は、従来と同様約8mm以下とするのが好ましい。
これは、粒径8mm超の粉鉄鉱石は焼成塊成鉱化し
ないでもそのまま使用でき、焼成塊成鉱化する必
要があるのは粒径8mm以下の粉鉄鉱石であるから
である。
この発明において、生ペレツトの粒径は、従来
と同様約3〜13mmとするのが好ましい。その理由
は、次の通りである。即ち、生ペレツトの粒径が
3mm未満であると、焼成炉における生ペレツトの
焼成時に、粉コークスの燃焼によつて生じた高温
燃焼ガスが、生ペレツトの層を円滑に通過するの
を阻害されるため、焼成塊成鉱の生産率がが低下
する問題が生ずる。のみならず、単体の焼成ペレ
ツトの形の焼成塊成鉱も粒径3mm未満となるため
に、このような小さい粒径の焼成塊成鉱を高炉内
に装入した場合に、還元ガスの円滑な通過を阻害
する。その結果、高炉内において棚吊りおよびス
リツプが発生し、高炉操業が不安定になる問題が
生ずる。一方、生ペレツトの粒径が13mmを超える
と、衝撃に対する抵抗力が弱くなるため、生ペレ
ツトを焼成炉に移送する際に、生ペレツトが崩壊
する問題を生ずる。のみならず、焼成塊成鉱の焼
成ペレツト個々の粒径も13mmを超えるため、この
ような大きい焼成ペレツトの焼成塊成鉱を高炉内
に装入した場合に、焼成塊成鉱の中心部まで還元
ガスが浸透するのに長時間を必要とする。その結
果、高炉内における焼成塊成鉱の還元性が悪くな
り、且つ、未還元の芯が残つて、焼成塊成鉱の、
荷重下における高温特性が悪くなる問題を生ず
る。
〔実施例〕
第1表に示す粒度構成を有し、第2表に示す化
学成分組成を有する5種類の銘柄の粉鉄鉱石A〜
Eを、この発明に従い、焼成塊成鉱中のSiO2含
有量が0.5〜5.0wt%の範囲内となるよう、第3表
に示すように、適宜の割合で配合した。比較のた
めに、焼成塊成鉱中のSiO2含有量が5.0wt%超と
なるよう、同じく、第3表に示すように、適宜の
割合で配合した。
[Technical Field of the Invention] The present invention relates to a method for producing calcined agglomerate ore suitable as a raw material for blast furnaces or directly reduced iron. [Prior art and its problems] As a raw material for blast furnaces or raw material for direct reduction steelmaking,
Calcined agglomerate, which is made by pelletizing powdered iron ore and calcining it, is known, and its use is expanding. This calcined agglomerate ore is usually produced as follows. That is, a solvent consisting of at least one of quicklime, slaked lime, limestone, bentonite, granulated blast furnace slag, dolomite, etc. is added to powdered iron ore with a particle size of about 8 mm or less, and CaO/SiO 2 in the calcined agglomerated ore is added to the powdered iron ore.
Add so that the value is about 1.0 to 2.5 and mix with a mixer. Then, the obtained mixture is supplied to a disk-type first granulator, water is added thereto, and the first
The mixture is granulated using a granulator, and formed into raw pellets having a particle size of, for example, about 3 to 13 mm. Next, the obtained raw pellets are supplied to a second disk-type granulator, and about 2.5 to 4.0 wt% of coke powder is added, and the raw pellets are further granulated by the second granulator. In this way, raw pellets whose surfaces are coated with coke powder are prepared. Then, the raw pellets obtained in this way are charged into an endless moving grate type kiln, and the layer of charged raw pellets is placed on the grate of the kiln, and the drying zone of the kiln is heated. Pass through the band and firing zone in sequence. In the drying zone, drying gas at a temperature of 150 to 350°C is blown into the layer of raw pellets from above to dry the raw pellets. At the ignition zone,
High-temperature combustion gas is blown into the layer of dried raw pellets from above to ignite the coke powder on the surface of the raw pellets. In the combustion zone, the hot combustion gas produced by the combustion of coke breeze is drawn downward through the bed of green pellets to heat the green pellets to the calcination temperature. The raw pellets are calcined by heating in a calcining zone into large blocks of calcined agglomerates consisting of calcined pellets bound together by at least one of calcium ferrite and slag formed on their surfaces. . The calcined agglomerate ore in the form of large blocks thus obtained is discharged from the downstream end of the calciner, crushed by a crusher, and then sieved by a screen, with a particle size of less than 3 mm. The sifted calcined agglomerate pieces are removed, and thus the calcined agglomerate ore in the form of a lump of multiple calcined pellets with a maximum particle size of about 50 mm and the particle size of a single calcined pellet in the form of 3 to 13 mm. A certain amount of calcined agglomerate ore is produced. The calcined agglomerate produced in the manner described above has excellent reducing properties, since it mainly contains a large amount of fine calcium ferrite and fine hematite, which have excellent reducing properties. In addition, not only when a plurality of fired pellets are combined into a lump, but also when a single fired pellet has an irregular shape, when charged into a blast furnace, Because it does not flow unevenly to the center of the blast furnace, and gaps are created between the fired agglomerated ores,
Smooth passage of reducing gas is not obstructed. Furthermore, even if it collapses due to shock during transportation,
Since the calcined agglomerate, which is in the form of a lump made up of a plurality of calcined pellets combined, is simply separated into single calcined pellets, it can be used without any problems. However, conventional calcined agglomerates have SiO2 of 5.5
Since it contained about 6.0wt%, the reduction rate was 60~
The reduction rate was low at around 70%, and the reduction powdering rate was high at around 35-45%. In addition, calcined agglomerates have SiO2 of 5.5~
Since it contains about 6.0 wt%, the slag ratio in the blast furnace is high, for example, 360 kg/ton, and the fuel ratio (or coke ratio) is also high, for example, 520 kg/ton. [Object of the invention] In view of the above-mentioned current situation, the present invention has been developed by adding a solvent to powdered iron ore, granulating a mixed mixture to form raw pellets, coating the obtained raw pellets with coke powder, The purpose is to improve the reduction rate and reduction powdering rate of calcined agglomerate ore when the raw pellets are charged into an endless moving grate type kiln to continuously produce calcined agglomerate ore. be. [Summary of the Invention] This invention involves adding a solvent to powdered iron ore, granulating the mixture in a disc-type granulator to form raw pellets, and coating the obtained raw pellets with coke powder. , in a method for producing fired agglomerate ore, in which the raw pellets are charged into an endless moving grate kiln and fired continuously, thus continuously producing fired agglomerate ore, as the powdered iron ore, in the calcined agglomerate ore.
It is characterized by the use of powdered iron ore containing 0.5 to 5.0 wt% of SiO 2 . [Structure of the Invention] Hereinafter, the method for producing calcined agglomerates of the present invention will be described in detail. The present inventors added a solvent to powdered iron ore, granulated the mixed mixture to form raw pellets, coated the obtained raw pellets with coke powder, and fired the raw pellets using an endless moving grate. Charge it into the furnace,
In order to continuously produce calcined agglomerate ore, we have conducted intensive research to improve the reduction rate and reduction powdering rate of calcined agglomerate ore. Conventionally, fired agglomerate ores contained 5.0 to 6.0 wt% of SiO 2 because, when raw pellets were fired, SiO 2 in fine iron ore formed slag with CaO in the solvent. In order to combine powdered iron ores and form them into agglomerates, the SiO 2 content in the calcined agglomerates must be approximately
This is because it was believed that it was necessary for powdered iron ore to contain SiO 2 at a level of 5.0 wt% or more. However, as research progressed, it was discovered that a drum-type granulator was used to granulate powdered iron ore, and that powdered iron ore was granulated by adding not only a solvent but also coke powder. In the case of raw pellets,
A disk-type granulator is used to granulate the iron ore powder, and coke powder is coated on the surface of the iron ore powder after granulation, and only a solvent is added to the iron ore powder. In the case of raw pellets obtained by
It has good granulation properties and is formed into a good spherical lump, so even if the SiO 2 content in the iron ore powder is low, the SiO 2 in the iron ore powder is mixed with the solvent in the iron ore when the raw pellets are fired. It was found that by forming slag with CaO, fine iron ore could be bonded together and agglomerated well. Therefore, it becomes possible to improve the reduction rate and reduction powdering rate of the calcined agglomerate ore. Therefore, the particle size of formulations with different SiO 2 contents is approximately 8
Experiments were conducted to produce calcined agglomerates by varying the SiO 2 content using raw pellets prepared from each type of fine iron ore with a diameter of less than mm. Then, the SiO 2 content, reduction rate, reduction powdering rate, product yield, and falling strength in the calcined agglomerate ore were investigated. As a result, the SiO 2 content in calcined agglomerate ore was reduced to 0.5~
It was found that when the content is 5.0 wt%, the reduction rate and reduction powdering rate of calcined agglomerate ore can be significantly improved, and the product yield and falling strength are not reduced. Figure 1 is a graph showing the relationship between the SiO 2 content and reduction rate in the obtained calcined agglomerate, and Figure 2 is a graph showing the relationship between the SiO 2 content and reduction rate. , FIG. 3 is a graph showing the relationship between SiO 2 content and fall strength, and FIG. 4 is a graph showing the relationship between SiO 2 content and fall strength.
It is a graph showing the relationship between SiO 2 content and product yield. As shown in Figure 1, the reduction rate of calcined agglomerates decreases as the SiO 2 content in the calcined agglomerates increases, but when the SiO 2 content is 0.5 to 5.0 wt%
Within the range, it is high at over 80%. When the SiO 2 content exceeds 5.0 wt%, the reduction rate drops rapidly below 80%. The reduction powdering rate of calcined agglomerate ore is
As shown in Figure 2, SiO 2 in the calcined agglomerates
When the SiO 2 content is in the range of 0.5 to 5.0 wt%, it is less than 30%, but when the SiO 2 content exceeds 5.0 wt%, the reduction powdering rate exceeds 30%. On the other hand, as shown in Figure 3, the fall strength of calcined agglomerates increases as the SiO 2 content in the calcined agglomerates increases, but when the SiO 2 content is 0.5
Even within the range of ~5.0wt%, the drop strength is approximately 85% or more and is sufficiently maintained. As shown in Figure 4, the product yield of calcined agglomerates increases as the SiO 2 content in the calcined agglomerates increases, but when the SiO 2 content is in the range of 0.5 to 5.0 wt%. The product yield is approximately 75% or more, which is maintained satisfactorily. In addition, in the above, the lower limit of SiO 2 content in calcined agglomerate ore is set to 0.5wt% because the SiO 2 content is
This is because it is almost difficult to obtain calcined agglomerates with a content of less than 0.5 wt% from the viewpoint of the quality of fine iron ore, and less than 0.5 wt% is practically meaningless. Therefore, in order to achieve a reduction rate of 80% or more and a reduction powdering rate of 30% or less of calcined agglomerate ore without reducing the product yield and falling strength of the calcined agglomerate ore, it is necessary to As iron ore, in calcined agglomerate ore
Powdered iron ore blended to have a SiO 2 content of 0.5 to 5.0 wt% should be used. In this invention, as described above, as the fine iron ore used for calcination, the fine iron ore blended so that the SiO 2 content in the calcined agglomerate is 0.5 to 5.0 wt% is used. This greatly improves the reduction rate and reduction powdering rate of agglomerate ore. In this invention, the amount of coke powder coated on the raw pellets is preferably 2.5 to 4.0 wt%, as in the conventional method. This means that the amount of coke powder to be coated is
This is because if the amount is less than 2.5wt%, the firing efficiency of the raw pellets in the kiln cannot be increased, and the raw pellets cannot be fired into high-strength fired agglomerates in a short time, and the amount of coke powder to be coated is 4.0wt. %, the temperature of the raw pellets during calcination becomes too high, and the structure of the calcined agglomerates becomes dense and has few pores. This is because the structure contains many rectangular calcium ferrites. In this invention, the particle size of the powdered iron ore used is preferably about 8 mm or less, as in the prior art.
This is because fine iron ore with a particle size of more than 8 mm can be used as is without being converted into calcined agglomerate minerals, and it is iron ore fines with a particle size of 8 mm or less that needs to be converted into calcined agglomerate minerals. In this invention, the particle size of the raw pellets is preferably about 3 to 13 mm, as in the conventional method. The reason is as follows. That is, if the particle size of the green pellets is less than 3 mm, the high-temperature combustion gas generated by the combustion of coke breeze will be inhibited from smoothly passing through the layer of green pellets when the green pellets are fired in the firing furnace. As a result, the production rate of calcined agglomerate ore decreases. In addition, since fired agglomerate ore in the form of single fired pellets has a particle size of less than 3 mm, when such small particle size calcined agglomerate is charged into a blast furnace, it is difficult for the reducing gas to flow smoothly. impede passage. As a result, shelving and slipping occur in the blast furnace, resulting in the problem of unstable blast furnace operation. On the other hand, if the particle size of the green pellets exceeds 13 mm, the resistance to impact becomes weak, resulting in the problem of the green pellets collapsing when they are transferred to a kiln. Not only that, the grain size of each fired pellet of fired agglomerate ore exceeds 13 mm, so when such large fired pellets of fired agglomerate ore are charged into a blast furnace, it is difficult to reach the center of the fired agglomerate ore. It takes a long time for the reducing gas to penetrate. As a result, the reducibility of the calcined agglomerate in the blast furnace deteriorates, and unreduced cores remain, resulting in
A problem arises in that the high temperature characteristics under load deteriorate. [Example] Five brands of fine iron ore A~ having the particle size composition shown in Table 1 and the chemical composition shown in Table 2
According to the present invention, E was blended in an appropriate ratio as shown in Table 3 so that the SiO 2 content in the calcined agglomerate was within the range of 0.5 to 5.0 wt%. For comparison, the calcined agglomerates were blended in appropriate proportions as shown in Table 3 so that the SiO 2 content was more than 5.0 wt%.
【表】【table】
【表】【table】
【表】【table】
【表】
次いで、これらの配合の粉鉄鉱石に媒溶剤およ
びバインダーとして、第4表に示す粒度構成の生
石灰を1.0〜2.7wt%添加、混合し、また塩基度調
整用として表5に示す粒度構成の石灰石を用い、
塩基度を1.8〜2.2の範囲に調整した。ここで得ら
れた混合物をデイスク型の造粒機で造粒して、第
6表に示す粒径分布を有する、水分含有量8〜
9wt%の生ペレツトに成形した。[Table] Next, 1.0 to 2.7 wt% of quicklime with the particle size composition shown in Table 4 was added and mixed as a solvent and binder to the powdered iron ore of these formulations, and the particle size shown in Table 5 was added for basicity adjustment. Using limestone of composition,
The basicity was adjusted to a range of 1.8-2.2. The mixture obtained here is granulated using a disk-type granulator, and the mixture has a particle size distribution shown in Table 6 and has a water content of 8 to 8.
It was formed into 9wt% raw pellets.
【表】【table】
【表】【table】
【表】
次いで、第7表に示す粒度構成の粉コークスを
生ペレツトに3.5wt%添加して造粒し、生ペレツ
トに粉コークスを被覆した。[Table] Next, 3.5 wt % of coke powder having the particle size composition shown in Table 7 was added to the raw pellets for granulation, and the raw pellets were coated with the coke powder.
【表】
そして、無端移動グレート式焼成炉のグレート
上に生ペレツトを400mmの厚さに装入して、生ペ
レツトを焼成炉の乾燥帯、点火帯および焼成帯を
順次移動させ、焼成塊成鉱に焼成した。そして、
このようにして得られた大きいブロツク状の焼成
塊成鉱を焼成炉の下流端から排出し、クラツシヤ
ーによつて破砕したのち、スクリーンによつて粒
径3mm未満の篩下の焼成塊成鉱片を除去し、かく
して、複数個の焼成ペレツトが結合した最大粒径
50mmの塊状の形の焼成塊成鉱および単体の焼成ペ
レツトの形の粒径3〜50mmの焼成塊成鉱が製造さ
れた。
以上のように製造された焼成塊成鉱中のSiO2
含有量および焼成塊成鉱の還元率等を第8表に示
す。[Table] Then, raw pellets are charged to a thickness of 400 mm onto the grate of an endless moving grate type kiln, and the raw pellets are sequentially moved through the drying zone, ignition zone, and firing zone of the kiln, and are baked into agglomerates. Fired into ore. and,
The large blocks of calcined agglomerate ore thus obtained are discharged from the downstream end of the kiln, and after being crushed by a crusher, the calcined agglomerate pieces under the sieve with a particle size of less than 3 mm are passed through a screen. is removed, thus reducing the maximum particle size of multiple calcined pellets combined.
Calcined agglomerates in the form of blocks of 50 mm and calcined agglomerates in the form of single calcined pellets with grain sizes of 3 to 50 mm were produced. SiO 2 in the calcined agglomerate produced as above
Table 8 shows the content and reduction rate of calcined agglomerates.
【表】【table】
【表】
第8表に示されるように、焼成塊成鉱中の
SiO2含有量がこの発明の範囲内である本発明No.
1〜6においては、いずれも焼成塊成鉱の還元率
および還元粉化率が良好で、落下強度および成品
歩留りを低下させることなく、還元率および還元
粉化率が向上されている。これに対し、焼成塊成
鉱中のSiO2含有量がこの発明の範囲外である比
較例No.7〜8においては、いずれも、焼成塊成鉱
の落下強度および成品歩留りは良いものの、還元
率および還元粉化率が悪化している。
〔発明の効果〕
この発明によれば、焼成塊成鉱の還元率および
還元粉化率を容易に向上させることができる。[Table] As shown in Table 8, the
Invention No. whose SiO 2 content is within the scope of this invention.
In Nos. 1 to 6, the reduction rate and reduction pulverization rate of the calcined agglomerates are good, and the reduction rate and reduction pulverization rate are improved without lowering the drop strength and product yield. On the other hand, in Comparative Examples Nos. 7 and 8, in which the SiO 2 content in the calcined agglomerates is outside the range of the present invention, although the falling strength and product yield of the calcined agglomerates are good, The reduction rate and reduction powdering rate have deteriorated. [Effects of the Invention] According to the present invention, the reduction rate and reduction powdering rate of calcined agglomerated ore can be easily improved.
第1図は、得られた焼成塊成鉱中のSiO2含有
量と還元率との関係を示すグラフ、第2図は、同
じく、SiO2含有量と還元粉化率との関係を示す
グラフ、第3図は、同じく、SiO2含有量と落下
強度との関係を示すグラフ、第4図は、同じく、
SiO2含有量と成品歩留りとの関係を示すグラフ
である。
Figure 1 is a graph showing the relationship between the SiO 2 content and reduction rate in the obtained calcined agglomerate, and Figure 2 is a graph showing the relationship between the SiO 2 content and reduction rate. , FIG. 3 is a graph showing the relationship between SiO 2 content and fall strength, and FIG. 4 is a graph showing the relationship between SiO 2 content and fall strength.
It is a graph showing the relationship between SiO 2 content and product yield.
Claims (1)
デイスク型の造粒機で造粒して生ペレツトを成形
し、得られた生ペレツトに粉コークスを被覆し、
前記生ペレツトを無端移動グレート式焼成炉に装
入して連続的に焼成し、かくして、焼成塊成鉱を
連続的に製造する、焼成塊成鉱の製造方法におい
て、 前記粉鉄鉱石として、焼成塊成鉱中のSiO2が
0.5〜5.0wt%となるように配合した粉鉄鉱石を使
用することを特徴とする、焼成塊成鉱の製造方
法。[Scope of Claims] 1 A mixture of powdered iron ore and a solvent is added and mixed and granulated using a disk-type granulator to form raw pellets, and the resulting raw pellets are coated with coke powder,
A method for producing fired agglomerate ore, in which the raw pellets are charged into an endless moving grate kiln and fired continuously, thereby continuously producing fired agglomerate ore, wherein the iron ore powder is a calcined agglomerate. SiO 2 in agglomerate ore
A method for producing calcined agglomerate ore, characterized by using powdered iron ore blended to have a content of 0.5 to 5.0 wt%.
Priority Applications (12)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP29669386A JPS63153225A (en) | 1986-12-15 | 1986-12-15 | Method for producing calcined agglomerate |
| AU82221/87A AU600777B2 (en) | 1986-12-15 | 1987-12-08 | Method for manufacturing agglomerates of fired pellets |
| IN357/BOM/87A IN167132B (en) | 1986-12-15 | 1987-12-08 | |
| CA000554134A CA1324493C (en) | 1986-12-15 | 1987-12-11 | Method for manufacturing agglomerates of fired pellets |
| US07/131,660 US4851038A (en) | 1986-12-15 | 1987-12-11 | Method for manufacturing agglomerates of fired pellets |
| EP93111020A EP0578253B1 (en) | 1986-12-15 | 1987-12-14 | Method for manufacturing agglomerates of fired pellets |
| DE3751747T DE3751747T2 (en) | 1986-12-15 | 1987-12-14 | Process for producing briquettes from burned pellets |
| EP87118525A EP0271863B1 (en) | 1986-12-15 | 1987-12-14 | Method for manufacturing agglomerates of fired pellets |
| DE3752270T DE3752270T2 (en) | 1986-12-15 | 1987-12-14 | Process for producing briquettes from burned pellets |
| BR8706790A BR8706790A (en) | 1986-12-15 | 1987-12-14 | PROCESS FOR THE PRODUCTION OF BURNED PELLETS PELLETS |
| KR1019870014415A KR910001325B1 (en) | 1986-12-15 | 1987-12-15 | Manufacturing method of nodule of fired pellet |
| CN87108122A CN1016184B (en) | 1986-12-15 | 1987-12-15 | Method for producing sintered pellet |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP29669386A JPS63153225A (en) | 1986-12-15 | 1986-12-15 | Method for producing calcined agglomerate |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS63153225A JPS63153225A (en) | 1988-06-25 |
| JPH0425327B2 true JPH0425327B2 (en) | 1992-04-30 |
Family
ID=17836861
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP29669386A Granted JPS63153225A (en) | 1986-12-15 | 1986-12-15 | Method for producing calcined agglomerate |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS63153225A (en) |
-
1986
- 1986-12-15 JP JP29669386A patent/JPS63153225A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS63153225A (en) | 1988-06-25 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| LAPS | Cancellation because of no payment of annual fees |