JPH0430446B2 - - Google Patents
Info
- Publication number
- JPH0430446B2 JPH0430446B2 JP29844286A JP29844286A JPH0430446B2 JP H0430446 B2 JPH0430446 B2 JP H0430446B2 JP 29844286 A JP29844286 A JP 29844286A JP 29844286 A JP29844286 A JP 29844286A JP H0430446 B2 JPH0430446 B2 JP H0430446B2
- Authority
- JP
- Japan
- Prior art keywords
- ore
- calcined
- added
- quicklime
- iron ore
- 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
- ODINCKMPIJJUCX-UHFFFAOYSA-N Calcium oxide Chemical compound [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 claims description 94
- 239000008188 pellet Substances 0.000 claims description 62
- 239000000292 calcium oxide Substances 0.000 claims description 47
- 235000012255 calcium oxide Nutrition 0.000 claims description 47
- 239000012256 powdered iron Substances 0.000 claims description 35
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 25
- 239000000203 mixture Substances 0.000 claims description 14
- 239000002904 solvent Substances 0.000 claims description 14
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 13
- 229910052742 iron Inorganic materials 0.000 claims description 12
- 238000004519 manufacturing process Methods 0.000 claims description 10
- 238000001354 calcination Methods 0.000 claims description 7
- 229910004298 SiO 2 Inorganic materials 0.000 claims description 5
- 239000000843 powder Substances 0.000 claims description 5
- 239000011248 coating agent Substances 0.000 claims description 2
- 238000000576 coating method Methods 0.000 claims description 2
- 238000000034 method Methods 0.000 claims description 2
- 239000002245 particle Substances 0.000 description 23
- 238000005469 granulation Methods 0.000 description 6
- 230000003179 granulation Effects 0.000 description 6
- 230000001603 reducing effect Effects 0.000 description 6
- 235000019738 Limestone Nutrition 0.000 description 5
- 238000010304 firing Methods 0.000 description 5
- 239000006028 limestone Substances 0.000 description 5
- 238000002485 combustion reaction Methods 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 239000007789 gas Substances 0.000 description 4
- WETINTNJFLGREW-UHFFFAOYSA-N calcium;iron;tetrahydrate Chemical compound O.O.O.O.[Ca].[Fe].[Fe] WETINTNJFLGREW-UHFFFAOYSA-N 0.000 description 3
- 239000000571 coke Substances 0.000 description 3
- 239000000567 combustion gas Substances 0.000 description 3
- 238000007796 conventional method Methods 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 239000011230 binding agent Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 229910052595 hematite Inorganic materials 0.000 description 2
- 239000011019 hematite Substances 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- LIKBJVNGSGBSGK-UHFFFAOYSA-N iron(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Fe+3].[Fe+3] LIKBJVNGSGBSGK-UHFFFAOYSA-N 0.000 description 2
- 235000010755 mineral Nutrition 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 239000002893 slag Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- 235000012216 bentonite Nutrition 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 235000011116 calcium hydroxide Nutrition 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
- 229910000514 dolomite Inorganic materials 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000005453 pelletization Methods 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 238000009628 steelmaking Methods 0.000 description 1
Landscapes
- Manufacture And Refinement Of Metals (AREA)
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、媒溶
剤として生石灰および消石灰、石灰石、ベントナ
イト、高炉水砕スラグ、ドロマイト等を、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に着
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。
ところで、粉鉄鉱石に添加される媒溶剤のうち
生石灰は、粉鉄鉱石を生ペレツトに造粒する際に
バインダーとしての作用を有している。このた
め、生石灰は前述したように必ず添加されている
が、従来は、粉鉄鉱石に3.0〜10.0wt%も多量に
添加していたため、生石灰の費用増大が無視し得
ず、焼成塊成鉱の価格を高いものにしていた。
〔発明の目的〕
この発明は、上述の現状に鑑み、粉鉄鉱石に生
石灰およびその他の媒溶剤を添加、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、粉鉄鉱石に添
加する生石灰の添加量を選択することによつて、
焼成塊成鉱の成品歩留り等を低化させることな
く、焼成塊成鉱の製造コスト低減を可能にするこ
とを目的とするものである。
〔発明の概要〕
この発明は、粉鉄鉱石に生石灰およびその他の
媒溶剤を、焼成塊成鉱中のCaO/SiO2の値が1.0
〜2.5となるように添加、混合した混合物を、デ
イスク型の造粒機によつて造粒して、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、
前記粉鉄鉱石に添加する前記生石灰およびその
他の媒溶剤のうち前記生石灰の、前記粉鉄鉱石へ
の添加物が1.0〜2.5wt%であ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、粉鉄鉱石に生石灰およびその他
の媒溶剤を添加、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、焼成塊成鉱の製造コストを低減す
べく、粉鉄鉱石への生石灰の添加量について研究
を重ねた。
従来、粉鉄鉱石に3.0〜10.0wt%もの多量の生
石灰を添加していたのは、粉鉄鉱石を生ペレツト
に造粒する際に、造粒効果を高めるために多量の
生石灰を添加する必要が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
生石灰およびその他の媒溶剤のみならず粉コーク
スをも添加して、生ペレツトに造粒する場合なら
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
後に生ペレツトの表面に被覆するようにし、粉鉄
鉱石には生石灰およびその他の媒溶剤のみを添加
して、生ペレツトに造粒する場合には、生ペレツ
トの造粒性が良いので、粉鉄鉱石への生石灰の添
加量が少なくても、容易に粉鉄鉱石を生ペレツト
に成形できることが判つた。従つて、焼成塊成鉱
の製造コストを低減することが可能となる。
ただ、その場合、生石灰の添加量が少なにこと
により、焼成塊成鉱の成品歩留りおよび落下強度
が低くなる虞れがある。そこで、粉鉄鉱石への生
石灰の添加量を変化させて、粉鉄鉱石に生石灰お
よびその他の媒溶剤を添加し、造粒によつて生ペ
レツトを成形して、生ペレツトを焼成塊成鉱に焼
成する製造実験を行ない、そのときの生石灰の添
加量と焼成塊成鉱の成品歩留りおよび落下強度と
の関係を調べた。
その結果、粉鉄鉱石への生石灰の添加量を1.0
〜2.5wt%とすれば、焼成塊成鉱の成品歩留りお
よび落下強度を充分に高く維持できることが判つ
た。
第1図は、粉鉄鉱石への生石灰の添加量と得ら
れた焼成塊成鉱の成品歩留りとの関係を示すグラ
フ、第2図は、粉鉄鉱石への生石灰の添加量と得
られた焼成塊成鉱の落下強度との関係を示すグラ
フである。なお、粉鉄鉱石の粒径は約8mm以下、
生ペレツトの粒径は約3〜13mm、粉コークスの添
加量は3.5wt%の条件で行なつた。
第1図に示されるように、焼成塊成鉱の成品歩
留りは、粉鉄鉱石への生石灰の添加量が多くなる
につれて増大しており、添加量が1.0wt%以上で
は成品歩留りは75%以上になつている。生石灰の
添加量が2.5wt%を超えると、成品歩留りは85%
を上廻つて高くなるが、その高くなる程度は小さ
く、生石灰の添加量が多くなるデメリツトが増大
する。焼成塊成鉱の落下強度は、第2図に示され
るように、粉鉄鉱石への生石灰の添加量が多くな
るにつれて増大しており、添加量が1.0wt%以上
では落下強度は85%以上になつている。生石灰の
添加量が2.5wt%を超えると、落下強度は90%を
上廻つて高くなるが、その高くなる程度は同様に
小さい。
従つて、焼成塊成鉱の成品歩留りを75%以上、
落下強度を85%以上に維持し、且つ、粉鉄鉱石へ
の生石灰の添加量を少なくするためには、粉鉄鉱
石への生石灰の添加量を1.0〜2.5wt%とすべきで
ある。
この発明においては、以上のように、粉鉄鉱石
への生石灰の添加量を1.0〜2.5wt%として、焼成
塊成鉱の成品歩留りおよび落下強度を高く維持し
たままで、生石灰の添加量を従来より少なくする
ものである。なお、粉鉄鉱石への生石灰と共に石
灰石等のその他の媒溶剤を添加して、焼成塊成鉱
中のCaO/SiO2の値が1.0〜2.5となるように塩基
調整することは、言うまでもない。
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
焼成効率も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、また、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、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。また焼成過程でペレツトの中
心温度が十分高くならないうちに冷却されるた
め、特に中心部の品質が悪化することが認められ
ている。さらに、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表に示す粒度構成で第2表に示す化学成分
組成の微粉鉄鉱石と、第3表に示す粒度構成で第
4表に示す化学成分組成の粗粒鉄鉱石とを、微粉
鉄鉱石40wt%、粗粒鉄鉱石60wt%の割合で使用
し、これに媒溶剤およびバインダーとして第5表
に示す粒度構成の生石灰を、この発明の範囲内の
添加量で添加し、更にその他の媒溶剤として石灰
石を添加して、焼成塊成鉱中のCaO/SiO2の値
が1.0〜2.5となるように塩基度調整した。比較の
ために、粉鉄鉱石に生石灰を、この発明の範囲外
の添加量で添加し、同様に更に石灰石を添加して
塩基度調整した。そして、これらの生石灰および
石灰石が添加された粉鉄鉱石を混合したのち、デ
イスク型の造粒機によつて造粒して、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。
[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, powdered iron ore with a particle size of about 8 mm or less is mixed with quicklime, slaked lime, limestone, bentonite, granulated blast furnace slag, dolomite, etc. as a solvent, and the value of CaO/SiO 2 in the calcined agglomerate ore is about 1.0 to 2.5. Add and mix with a mixer. Then, the obtained mixture is supplied to a disk-type first granulator, water is added, and the mixture is granulated by the first granulator to form raw pellets with a particle size of, for example, about 3 to 13 mm. Shape. 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, igniting 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. Incidentally, among the solvents added to powdered iron ore, quicklime acts as a binder when powdered iron ore is granulated into green pellets. For this reason, quicklime is always added as mentioned above, but in the past, a large amount of 3.0 to 10.0 wt% was added to powdered iron ore, so the increased cost of quicklime could not be ignored, and the made the price high. [Purpose of the Invention] In view of the above-mentioned current situation, the present invention has been developed by granulating a mixture of powdered iron ore with quicklime and other solvents, forming raw pellets, and adding powder to the obtained raw pellets. By selecting the amount of quicklime added to powdered iron ore when coating coke and charging the green pellets into an endless moving grate type kiln to continuously produce burned agglomerate ore. ,
The purpose of this invention is to make it possible to reduce the manufacturing cost of calcined agglomerate ore without lowering the product yield of calcined agglomerate ore. [Summary of the Invention] This invention is based on the invention, in which quicklime and other solvents are added to powdered iron ore, and the CaO/SiO 2 value in the calcined agglomerate ore is 1.0.
The mixture was added and mixed so as to have a concentration of ~2.5, and the mixture was granulated using a disc-type granulator to form raw pellets, the resulting raw pellets were coated with coke powder, and the raw pellets were made into endless pellets. A method for producing calcined agglomerate ore, in which the calcined agglomerate ore is continuously produced by charging into a moving grate calcining furnace and continuously calcining the calcined ore. Among the solvents, the additive of the quicklime to the powdered iron ore is 1.0 to 2.5 wt%. [Structure of the Invention] Hereinafter, the method for producing calcined agglomerates of the present invention will be described in detail. The present inventors added quicklime and other solvents to powdered iron ore, granulated the mixture to form raw pellets, coated the obtained raw pellets with coke powder, and made the raw pellets into endless powder. In order to reduce the manufacturing cost of calcined agglomerate ore when it is charged into a moving grate kiln and continuously produce calcined agglomerate ore, we have conducted repeated research on the amount of quicklime added to powdered iron ore. Conventionally, a large amount of quicklime (3.0 to 10.0wt%) was added to powdered iron ore.The reason is that when powdered iron ore is granulated into raw pellets, it is necessary to add a large amount of quicklime to enhance the granulation effect. This is because it was said that there was. However, as research progressed, it was discovered that a drum-type granulator was used to granulate powdered iron ore, and that not only quicklime and other solvents but also coke powder was added to the powdered iron ore. Regardless of the case of granulation, a disk-type granulator is used to granulate powdered iron ore, and coke powder is coated on the surface of raw pellets after granulation of powdered iron ore. When granulating into raw pellets by adding only quicklime and other solvents, the granulation properties of the raw pellets are good, so even if the amount of quicklime added to powdered iron ore is small, it can be easily powdered. It was discovered that iron ore could be formed into raw pellets. Therefore, it is possible to reduce the manufacturing cost of calcined agglomerated ore. However, in that case, there is a risk that the product yield and falling strength of the calcined agglomerate ore will be low due to the small amount of quicklime added. Therefore, we changed the amount of quicklime added to powdered iron ore, added quicklime and other solvents to powdered iron ore, formed raw pellets through granulation, and turned the raw pellets into calcined agglomerates. A firing production experiment was conducted to investigate the relationship between the amount of quicklime added and the product yield and falling strength of fired agglomerate ore. As a result, the amount of quicklime added to powdered iron ore was reduced to 1.0
It has been found that by setting the content to 2.5 wt%, the product yield and falling strength of calcined agglomerates can be maintained sufficiently high. Figure 1 is a graph showing the relationship between the amount of quicklime added to powdered iron ore and the yield of the obtained calcined agglomerates, and Figure 2 is a graph showing the relationship between the amount of quicklime added to powdered iron ore and the yield of the obtained calcined agglomerates. It is a graph which shows the relationship with the falling strength of calcined agglomerate ore. In addition, the particle size of powdered iron ore is approximately 8 mm or less,
The particle size of the raw pellets was approximately 3 to 13 mm, and the amount of coke powder added was 3.5 wt%. As shown in Figure 1, the product yield of calcined agglomerate ore increases as the amount of quicklime added to fine iron ore increases, and when the addition amount is 1.0wt% or more, the product yield exceeds 75%. It's getting old. When the amount of quicklime added exceeds 2.5wt%, the product yield is 85%.
However, the degree of increase is small and the disadvantage of increasing the amount of quicklime added increases. As shown in Figure 2, the falling strength of calcined agglomerates increases as the amount of quicklime added to powdered iron ore increases, and when the amount added is 1.0wt% or more, the falling strength is 85% or more. It's getting old. When the amount of quicklime added exceeds 2.5 wt%, the drop strength increases to more than 90%, but the degree of increase is similarly small. Therefore, the product yield of calcined agglomerate ore should be increased to 75% or more.
In order to maintain the fall strength at 85% or more and to reduce the amount of quicklime added to powdered iron ore, the amount of quicklime added to powdered iron ore should be 1.0 to 2.5 wt%. In this invention, as described above, the amount of quicklime added to powdered iron ore is set at 1.0 to 2.5 wt%, and the amount of quicklime added is increased from the conventional amount while maintaining the finished product yield and falling strength of the calcined agglomerates at a high level. It is to make it less. It goes without saying that other solvents such as limestone are added to the powdered iron ore together with quicklime to adjust the base so that the value of CaO/SiO 2 in the calcined agglomerated ore is 1.0 to 2.5. In this invention, the particle size of the powdered iron ore used is preferably about 8 mm or less, as in the conventional method.
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 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
If the amount is less than 2.5 wt%, the firing efficiency of raw pellets in the kiln cannot be increased, and the raw pellets cannot be fired into high-strength fired agglomerates in a short time. 4.0wt%
If the temperature exceeds , the temperature of the raw pellets during firing becomes too high, and the structure of the fired agglomerate becomes dense and has few pores, and at the same time it becomes a molten type structure with poor reducibility, i.e., secondary hematite or strip-shaped structure. This is because the tissue is rich in calcium ferrite. 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 within 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. It has also been observed that during the calcination process, the pellets are cooled before the center temperature reaches a sufficiently high temperature, resulting in a deterioration in quality, especially in the center. Furthermore, since the particle size of each fired pellet of fired agglomerate ore exceeds 13 mm, when such large fired agglomerate ore is charged into a blast furnace, the reducing gas reaches the center of the fired agglomerate ore. It takes a long time to penetrate. As a result, the reducibility of the calcined agglomerate ore in the blast furnace deteriorates, and unreduced cores remain, resulting in a problem that the high temperature characteristics of the calcined agglomerate ore under load deteriorate. [Example] Fine iron ore with the particle size composition shown in Table 1 and the chemical composition shown in Table 2, and coarse iron ore with the particle size structure shown in Table 3 and the chemical composition shown in Table 4, Fine iron ore is used at a ratio of 40 wt% and coarse iron ore is used at a ratio of 60 wt%, and quicklime having a particle size composition shown in Table 5 is added as a solvent and a binder in an amount within the range of this invention, and other Limestone was added as a solvent to adjust the basicity so that the CaO/SiO 2 value in the calcined agglomerate was 1.0 to 2.5. For comparison, quicklime was added to powdered iron ore in an amount outside the scope of the present invention, and limestone was similarly added to adjust the basicity. Then, after mixing the powdered iron ore to which quicklime and limestone have been added, it is granulated using a disk-type granulator to obtain a powder having a water content of 8 to 9 wt and having a particle size distribution shown in Table 6. % raw pellets.
【表】【table】
【表】【table】
【表】【table】
【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、点火帯および燃焼帯を
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約
50mmの塊状の形の焼成塊成鉱および単体の焼成ペ
レツトの形の粒径約3〜13mm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の成品歩留
りおよび落下強度並びに粉鉄鉱石への生石灰の添
加量を第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 combustion 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, and thus the maximum particle size of multiple calcined pellets combined is approximately
Calcined agglomerates in the form of blocks of 50 mm and calcined agglomerates in the form of single calcined pellets with grain sizes of approximately 3 to 13 mm were produced. Table 8 shows the product yield and falling strength of the calcined agglomerates produced as described above, as well as the amount of quicklime added to the fine iron ore.
この発明によれば、粉鉄鉱石に添加する生石灰
の添加量を選択することによつて、成品歩留り等
を低下させることなく、焼成塊成鉱を安価に製造
することが可能となる。
According to this invention, by selecting the amount of quicklime to be added to fine iron ore, it is possible to inexpensively produce calcined agglomerate ore without reducing the product yield.
第1図は、粉鉄鉱石への生石灰の添加量と得ら
れた焼成塊成鉱の成品歩留りとの関係を示すグラ
フ、第2図は、粉鉄鉱石への生石灰の添加量と得
られた焼成塊成鉱の落下強度との関係を示すグラ
フである。
Figure 1 is a graph showing the relationship between the amount of quicklime added to powdered iron ore and the yield of the obtained calcined agglomerates, and Figure 2 is a graph showing the relationship between the amount of quicklime added to powdered iron ore and the yield of the obtained calcined agglomerates. It is a graph which shows the relationship with the falling strength of calcined agglomerate ore.
Claims (1)
焼成塊成鉱中のCaO/SiO2の値が1.0〜2.5となる
ように添加、混合した混合物を、デイスク型の造
粒機によつて造粒して、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、 前記粉鉄鉱石に添加する前記生石灰およびその
他の媒溶剤のうち前記生石灰の、前記粉鉄鉱石へ
の添加量が1.0〜2.5wt%であることを特徴とす
る、焼成塊成鉱の製造方法。[Claims] 1. Adding quicklime and other solvents to powdered iron ore,
The mixture was added and mixed so that the CaO/SiO 2 value in the calcined agglomerate was 1.0 to 2.5, and the mixture was granulated using a disk-type granulator to form raw pellets. A method for producing calcined agglomerate ore, which comprises coating raw pellets with coke powder, charging the raw pellets into an endless moving grate type kiln, and continuously calcining them, thereby continuously producing calcined agglomerate ore. Production of calcined agglomerate ore, characterized in that, among the quicklime and other solvents added to the iron ore powder, the amount of the quicklime added to the iron ore powder is 1.0 to 2.5 wt%. Method.
Priority Applications (12)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61298442A JPS63153226A (en) | 1986-12-15 | 1986-12-15 | Method for producing calcined agglomerate |
| IN357/BOM/87A IN167132B (en) | 1986-12-15 | 1987-12-08 | |
| AU82221/87A AU600777B2 (en) | 1986-12-15 | 1987-12-08 | 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 |
| CA000554134A CA1324493C (en) | 1986-12-15 | 1987-12-11 | Method for manufacturing agglomerates of fired pellets |
| DE3751747T DE3751747T2 (en) | 1986-12-15 | 1987-12-14 | Process for producing briquettes from burned 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 |
| EP93111020A EP0578253B1 (en) | 1986-12-15 | 1987-12-14 | Method for manufacturing agglomerates of fired pellets |
| EP87118525A EP0271863B1 (en) | 1986-12-15 | 1987-12-14 | Method for manufacturing agglomerates of fired pellets |
| CN87108122A CN1016184B (en) | 1986-12-15 | 1987-12-15 | Method for producing sintered pellet |
| KR1019870014415A KR910001325B1 (en) | 1986-12-15 | 1987-12-15 | Manufacturing method of nodule of fired pellet |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61298442A JPS63153226A (en) | 1986-12-15 | 1986-12-15 | Method for producing calcined agglomerate |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS63153226A JPS63153226A (en) | 1988-06-25 |
| JPH0430446B2 true JPH0430446B2 (en) | 1992-05-21 |
Family
ID=17859761
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP61298442A Granted JPS63153226A (en) | 1986-12-15 | 1986-12-15 | Method for producing calcined agglomerate |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS63153226A (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103882223B (en) * | 2014-04-02 | 2016-03-30 | 山西太钢不锈钢股份有限公司 | A kind of method improving red soil nickel ore bursting temperature of pellet ores |
-
1986
- 1986-12-15 JP JP61298442A patent/JPS63153226A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS63153226A (en) | 1988-06-25 |
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