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JPS5818413B2 - A method for producing sintered ore that enables high blending of ores containing high Al↓2O↓3 - Google Patents
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JPS5818413B2 - A method for producing sintered ore that enables high blending of ores containing high Al↓2O↓3 - Google Patents

A method for producing sintered ore that enables high blending of ores containing high Al↓2O↓3

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Publication number
JPS5818413B2
JPS5818413B2 JP5070180A JP5070180A JPS5818413B2 JP S5818413 B2 JPS5818413 B2 JP S5818413B2 JP 5070180 A JP5070180 A JP 5070180A JP 5070180 A JP5070180 A JP 5070180A JP S5818413 B2 JPS5818413 B2 JP S5818413B2
Authority
JP
Japan
Prior art keywords
al2o3
sintered ore
ore
less
raw materials
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
Application number
JP5070180A
Other languages
Japanese (ja)
Other versions
JPS56146832A (en
Inventor
蟹沢秀雄
高田司
三国修
相馬英明
田代清
和島正巳
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nippon Steel Corp
Original Assignee
Nippon Steel Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Nippon Steel Corp filed Critical Nippon Steel Corp
Priority to JP5070180A priority Critical patent/JPS5818413B2/en
Publication of JPS56146832A publication Critical patent/JPS56146832A/en
Publication of JPS5818413B2 publication Critical patent/JPS5818413B2/en
Expired legal-status Critical Current

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Description

【発明の詳細な説明】 本発明は焼結鉱製造方法に関するものであり、焼結鉱の
品質や生産性を低下させることなく高Al2O3含有鉱
石の多量配合を可能ならしめた焼結鉱の製造を目的とす
るものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing sintered ore, in which a large amount of ore containing high Al2O3 can be blended without reducing the quality or productivity of the sintered ore. The purpose is to

高炉操業(こおいて炉況を安定化させ、生産性を高める
ためには、装入する原料の被還元性ができるだけ良く、
しかも炉内における強度、通気性が十分維持できる性状
を持つものでなければならない。
Blast furnace operation (in order to stabilize furnace conditions and increase productivity, the reducibility of the charged raw material must be as high as possible,
Moreover, it must have properties that allow it to maintain sufficient strength and ventilation inside the furnace.

高炉装入原料中鉄源としては塊鉄鉱石、ペレット、焼結
鉱が主であるが近年は焼結鉱の装入割合が80〜90%
と非常に高くなっており焼結鉱の品質が高炉操業を左右
するといっても過言ではない○ このため、被還元性が良く、炉内での強度が十分維持で
きる焼結鉱が望まれる。
The main sources of iron in blast furnace charging raw materials are lump iron ore, pellets, and sintered ore, but in recent years, the charging ratio of sintered ore has been 80 to 90%.
It is no exaggeration to say that the quality of sintered ore affects blast furnace operation. Therefore, sintered ore that has good reducibility and can maintain sufficient strength in the furnace is desired.

しかし、焼結鉱は一般に高炉炉内において400〜60
0℃のいわゆる低温還元領域tこおいて粉化する性質(
低温還元粉化性)を有し、高炉上部での通気を著しく阻
害する欠点がある。
However, sintered ore generally contains 400 to 60
The property of pulverizing in the so-called low-temperature reduction region t of 0°C (
It has the disadvantage of significantly inhibiting ventilation in the upper part of the blast furnace.

低温還元粉化の主な原因は、焼結過程てAl2O3゜T
i 02. MnO等を溶かし込んだ浴融部から晶出す
る多成分系へマクイトに起因すると考えられるが、とり
わけ多成分系へマクイト中の含有率の高いAl2OψS
最も問題である。
The main cause of low-temperature reduction powdering is Al2O3°T during the sintering process.
i02. It is thought that this is due to the multi-component system crystallized from the melted bath containing MnO, etc., but in particular, the high content of Al2OψS in the maquite causes the multi-component system to crystallize.
This is the most problematic.

この多成分系へマクイトは晶出時(こヘマタイト内部に
Al2O3等を析出し、この部分にヘマタイトからマグ
ネタイトに変わる際の結晶転移に伴う歪が集中しクラッ
クを発生する。
During crystallization of this multi-component system (Al2O3 etc. are precipitated inside hematite, strain due to crystal transition when hematite changes to magnetite concentrates in this part and cracks occur).

そして還元の進行と共にこの部分を起点として割れが成
長し粉化するので、これを防止する手段としてはコーク
スを増配合することにより焼結雰囲気の60分圧を高め
多成分マグネタイトの再酸化を抑制することが考えられ
る。
As the reduction progresses, cracks will grow starting from this area and turn into powder, so the means to prevent this is to increase the 60% partial pressure of the sintering atmosphere by adding more coke to suppress the re-oxidation of the multi-component magnetite. It is possible to do so.

しかし、この方法ではコークス原単位が悪化するので、
現在は多成分系へマクイト中に入るAl2O3量を抑え
る、即ち配合原料中のAl2O3量を制限することが行
われている。
However, this method worsens the coke consumption rate,
Currently, efforts are being made to suppress the amount of Al2O3 that enters maquito into multicomponent systems, that is, to limit the amount of Al2O3 in the blended raw materials.

配合原料中に含まれるAl2O3の増加は焼結鉱の低温
還元粉化性を悪化させるのみならず、Al2O3含有鉱
石は滓化性が悪いため融体生成(以下ボンドと称す)量
を減少させる。
An increase in Al2O3 contained in the blended raw materials not only deteriorates the low-temperature reduction powdering properties of the sintered ore, but also reduces the amount of melt produced (hereinafter referred to as bond) since Al2O3-containing ores have poor slagability.

このため焼結鉱の強度維持に必要なボンドの量が減少し
焼結鉱の成品歩留を悪化させる。
For this reason, the amount of bond required to maintain the strength of the sintered ore decreases, which deteriorates the product yield of the sintered ore.

この点からもAl2O3は有害成分であり、焼結鉱中の
Al2O3量は制限されるものである。
From this point of view as well, Al2O3 is a harmful component, and the amount of Al2O3 in sintered ore is limited.

しかし、Al2O3は配合原料中に特に添加するのでは
なく鉱石中から脈石分として持込まれるもので高Al2
O3系鉱石が近年のように多量輸入され、これ等の鉱石
を多使用せざるを得ない状態では焼結鉱のAl2O3の
上昇は避けがたく、低温還元粉化性、成品歩留の悪化を
防止し、かつ高Al2O3鉱石の多量使用技術の開発が
望まれている。
However, Al2O3 is not specifically added to the blended raw materials, but is brought in from the ore as gangue, and has a high Al2 content.
In recent years, large quantities of O3-based ores have been imported, and when these ores have to be used extensively, an increase in Al2O3 in sintered ore is unavoidable, leading to deterioration in low-temperature reduction powdering properties and product yield. It is desired to develop a technology that can prevent this and use large quantities of high-Al2O3 ore.

本発明はこのような事情に鑑みてなされたものであり、
粒径1朋未満の細粒部分を25重量%以上含有する配合
原料において、該配合原料中粒径0.25mm未満の微
粉部分に含まれる5i02量を配合原料を構成する成分
全体の0.85重量%以上とすると共に該微粉部分のA
403/S i 02重量比を0.25以下に調整し、
このように調整した配合原料を焼結することを特徴とす
る高Al2O3含有鉱石の高配合を可能とした焼結鉱の
製造方法である。
The present invention was made in view of these circumstances, and
In a blended raw material containing 25% by weight or more of fine particles with a particle size of less than 1 mm, the amount of 5i02 contained in the fine powder part with a particle diameter of less than 0.25 mm in the blended raw material is 0.85% of the total components constituting the blended raw material. At least % by weight and the A of the fine powder portion
Adjust the weight ratio of 403/S i 02 to 0.25 or less,
This is a method for producing sintered ore that enables a high blending of ore containing high Al2O3, which is characterized by sintering the blended raw materials prepared in this way.

以下本発明の詳細な説明する。The present invention will be explained in detail below.

一般に目溶性焼結鉱は酸化鉄粒子を融体が結合するいわ
ゆる溶融結合により塊成化される。
Generally, soluble sintered ore is agglomerated by so-called fusion bonding in which iron oxide particles are bonded together by a molten body.

焼結鉱品質、生産性などはこのボンドによって大きく左
右されるためどのようにしてボンドを生成させるかが極
めて重要である。
The quality of sintered ore, productivity, etc. are greatly influenced by this bond, so how to generate the bond is extremely important.

しかるに、ドワイトロイド型焼結機(以下DL型焼結機
と称する)1こよる焼結鉱製造方法に代表される充填層
吸気型式の現状焼結プロセスにおい。
However, in the current sintering process of the packed bed suction type, which is typified by the sintered ore production method using a Dwight Lloyd type sintering machine (hereinafter referred to as DL type sintering machine).

ては高温での反応時間が極めて短かいから、必要な融液
を短時間に迅速に生成せしめることが必要となる。
Since the reaction time at high temperatures is extremely short, it is necessary to quickly generate the necessary melt in a short period of time.

本発明者等はこの点について種々検討を加えた結果、配
合原料中0.25 mm未満の微粉部分の 。
As a result of various studies on this point, the present inventors found that the fine powder portion of less than 0.25 mm in the blended raw materials.

Al2O3及びS i 02含有量が重要であり、これ
らの値をコントロールすることにより迅速な融体生成を
促進し、それがひいては焼結鉱中のAJl?203含有
量を増加し得ることを見い出した。
The Al2O3 and S i 02 contents are important, and controlling these values promotes rapid melt formation, which in turn improves the AJl? It has been found that the 203 content can be increased.

一般に配合原料には6%程度の水分を含有させ。Generally, blended raw materials contain about 6% water.

て疑似粒化を促進することによって原料層の通気向上を
図っている。
The aim is to improve the ventilation of the raw material layer by promoting pseudo-granulation.

この疑似粒子は、1〜5mm程度の粗粒原料を核とし、
そのまわりに1u未満の細粒が付着する形をとっている
This pseudo-particle has a core of coarse raw material of about 1 to 5 mm,
It takes the form of fine particles of less than 1 u attached around it.

ところが、問題となる融液の生成は、この付着した細粒
のうち0、25 mm未満の微粉部分を起点として始ま
ることが本発明者等の検討により明らかとなった。
However, studies conducted by the present inventors have revealed that the production of the problematic melt starts from the part of the adhered fine particles smaller than 0.25 mm.

この初期融液は、次第にまわりの粗粒を溶かし込みなが
らその量を増加していくが、焼結時の高温滞留時間は短
かいので粗粒は完全に溶融せず、また融液も均一に混合
することなしに、初期融液の組成の影響を強く残したま
ま凝固が完了しボンドが形成される したがって、融液の必要量を迅速に確保するためには0
.25mm未満の微粉部分中に低融点組成の起点を増し
てやることが必要となる。
This initial melt gradually increases in volume while melting the surrounding coarse grains, but because the high temperature residence time during sintering is short, the coarse grains do not completely melt, and the melt is not uniform. Without mixing, solidification is completed and a bond is formed while retaining the strong influence of the composition of the initial melt. Therefore, in order to quickly secure the required amount of melt,
.. It is necessary to increase the starting point of the low melting point composition in the fine powder portion of less than 25 mm.

一方、焼結鉱中のAl2O3が増すと低温還元粉化指数
(以下RDIと称する)が悪化する傾向にあることはよ
く知られている。
On the other hand, it is well known that as the amount of Al2O3 in the sintered ore increases, the low temperature reduction index (hereinafter referred to as RDI) tends to deteriorate.

ところが統計的な傾向としてはAl2O3の悪影響がい
われているがAl2O3含有量が増してもRDIが必ず
しも悪化しない場合もみられ不明な点があった。
However, although it is said that there is an adverse effect of Al2O3 as a statistical tendency, there are some cases where the RDI does not necessarily worsen even if the Al2O3 content increases, so there are some unclear points.

本発明者等は前述のとおりボンドを形成するのは配合原
料中粒径0.25a!m未満の微粉部分であって粒径l
r/L11L以上の粗粒の多くは溶解せず焼は残った鉱
石(以下、元鉱と称する)として残存することから、A
403の影響を粗粒を含めた平均組成ではなく、微粉部
分のAl2O3量に着目して種々実験を繰り返した。
As mentioned above, the present inventors believe that the particle size of the blended raw materials that forms the bond is 0.25a! The fine powder part with a particle size of less than m
Most of the coarse grains with r/L of 11L or more are not dissolved and remain as residual ore (hereinafter referred to as original ore), so A
Various experiments were conducted focusing on the influence of 403 not on the average composition including coarse particles, but on the amount of Al2O3 in the fine powder portion.

その結果、配合原料中粒径0.25mm未満の微粉部分
のAl2O3含有量とRDIとの間をこは正の相関があ
ることを見い出した。
As a result, it was found that there is a positive correlation between the Al2O3 content of the fine powder portion with a particle size of less than 0.25 mm in the blended raw materials and RDI.

そして前記平均Al2O3量とRDIとの一部矛盾した
関係は0.25mm未満の微粉部分のAl2O3含有量
で説明できることがわかった。
It was also found that the partially contradictory relationship between the average Al2O3 amount and RDI can be explained by the Al2O3 content of the fine powder portion less than 0.25 mm.

従って、配合原料中のAl2O3量は平均組成ととも(
こ0.25 mm未満の微粉部分のAl2O3量も同時
に管理することが必要であり、鉄鉱石類を破砕して焼結
原料となす場合にはAl2O3含有量の高い鉱石の破砕
を避けることが焼結鉱のRDI維持にとって重要になる
Therefore, the amount of Al2O3 in the blended raw materials varies with the average composition (
It is also necessary to control the amount of Al2O3 in the fine powder part of less than 0.25 mm, and when iron ores are crushed to be used as raw materials for sintering, it is important to avoid crushing ores with high Al2O3 content. This is important for maintaining the RDI of the concretion.

以上の検討結果より、配合原料中の0.25mm未満の
微粉部分の量と組成就中S i 02 、 Al2O3
含有量が焼結鉱品質に重要な影響をおよぼすことが知ら
れた。
From the above study results, the amount of fine powder part less than 0.25 mm in the blended raw materials and the composition include S i 02 , Al2O3
It is known that the content has an important effect on the quality of sintered ore.

そして1rILm以上の粗粒部分のAl2O3の大部分
は未反応のまま残留するか、または反応しても一部分し
か反応に寄与しないことがわかった。
It was also found that most of the Al2O3 in the coarse grain portion of 1rILm or more remains unreacted, or even if reacted, only a portion contributes to the reaction.

したがって、0.25 mm未満の微粉部分の5i02
含有量を高めると共にAl2O3含有量を低減するよう
にそれぞれの値を適正に保持してやれば1間以上の粗粒
部分のAl2O3量が増加しても焼結鉱の品質、生産性
を損うことなしに焼結鉱を製造できる。
Therefore, 5i02 of the fine powder part less than 0.25 mm
If each value is maintained appropriately to increase the Al2O3 content and reduce the Al2O3 content, the quality and productivity of the sintered ore will not be impaired even if the amount of Al2O3 in the coarse grain portion increases by 1 or more. can produce sintered ore.

つまり、配合原料中0.25mm未満の微粉部分の量と
組成(SiO2,A1203)の適正条件が満足されれ
ば焼結鉱の品質、生産性にとっては必要十分であり、焼
結原料の111m以上の粗粒部分に含まれるAl2O3
量を増加しても焼結鉱の品質や生産性を損うことはない
In other words, if the appropriate conditions for the amount and composition (SiO2, A1203) of the fine powder part less than 0.25 mm in the blended raw material are satisfied, it is necessary and sufficient for the quality and productivity of the sintered ore. Al2O3 contained in the coarse part of
Even if the amount is increased, the quality and productivity of the sintered ore will not be impaired.

第1図は460mのDL型焼結機により焼結鉱を製造し
た実験結果であり配合原料中粒径0.25朋未満の微粉
部分に含まれるAl2O3と5i02量の重量比(以下
この値を−0,25朋中〔Al2O3/5i02]と称
する)が焼結鉱のEtDIと成品歩留にどのような影響
を与えるかを示した図である。
Figure 1 shows the experimental results of producing sintered ore using a DL type sintering machine with a length of 460 m.It shows the weight ratio of Al2O3 and 5i02 contained in the fine powder portion with a particle size of less than 0.25 mm in the blended raw materials (hereinafter this value will be referred to as FIG. 2 is a diagram showing how the EtDI of sintered ore and product yield are affected by -0,25 tomon [Al2O3/5i02].

第1図に示すようkc−0,25mm中〔Al2O3/
S i 02 ) とRDI、成品歩留との相関は強
く、−0,25mm中CAA203 /S i 02
:]の増加につれてRDI及び成品歩留はそれぞれ悪化
する。
As shown in Figure 1, [Al2O3/
There is a strong correlation between S i 02 ), RDI, and product yield, with CAA203 /S i 02 in -0.25 mm
: ] increases, RDI and product yield deteriorate, respectively.

とりわけ−0,25朋中〔Al2O3/SiO2〕が0
.25以下ではRDI及び成品歩留の悪化傾向はゆるや
かであるが0.25を超えるとRDI、成品歩留共急激
に悪化することがわかる。
Especially when -0,25 [Al2O3/SiO2] is 0
.. It can be seen that below 25, the RDI and product yield tend to deteriorate gradually, but when it exceeds 0.25, both RDI and product yield deteriorate rapidly.

この現象は焼結時の初期融液となる粒径0.25 mm
未満の微粉部分中にAl2O3がSiO2の25%を超
えて多量(こ存在する場合にはAl2O3の悪影響が顕
著に表われることを示している。
This phenomenon occurs when the particle size of the initial melt during sintering is 0.25 mm.
If Al2O3 is present in a large amount (more than 25% of SiO2) in the fine powder portion, the adverse effects of Al2O3 will be noticeable.

一方、初期融液量に大きく影響する0、25mm未満部
分の5i02量と焼結鉱の品質との関係を40ゆ試験鍋
により調査を行い、第2図に示すような結果を得た。
On the other hand, the relationship between the amount of 5i02 in the portions less than 0 and 25 mm, which greatly affects the initial melt amount, and the quality of the sintered ore was investigated using a 40 mm test pot, and the results shown in FIG. 2 were obtained.

即ち第2図は−0,25mm中〔Al2O3/5i02
]を0.20、コークス配合率を3.2重量%にそれぞ
れ固定して配合原料全体を構成する成分の合計(水分を
除く乾量)を100%とした値で表現して粒径0.25
rILrIL未満部分に含まれるSiO2重量%(以
下この値を−0,25mff1中S i 02 (%)
と称する)を種々変化させて−0,25Wtm中5i0
2(至)が焼結鉱のRDI及び成品歩留をこ与える影響
を示したものである。
In other words, Fig. 2 shows -0.25 mm [Al2O3/5i02
] is fixed at 0.20 and the coke blending ratio is fixed at 3.2% by weight, respectively, and the particle size is expressed as 100%, where the total of the components constituting the entire blended raw material (dry weight excluding water) is 100%. 25
SiO2 weight% contained in the portion less than rILrIL (hereinafter this value will be referred to as -0.25mff1 SiO2 (%)
5i0 in -0.25Wtm by variously changing
2 (to) shows the influence on the RDI and product yield of sintered ore.

第2図に示すよう【こ−0,25mm中5i02(%)
の増加に伴ってRDI及び成品歩留は共に改善され、特
に−0,25rILTIL中S i 02 (%)が0
.85以上では、RDI及び成品歩留が著しく改善され
る 以上第1図及び第2図に示したように焼結鉱のRDI、
成品歩留を良好に維持するためには配合原料の−0,2
5rItm中〔Al2O3/SiO□〕を0.25以下
にすると共に−0,25van中5in2(%)を0.
85以上にすることが重要であることがわかる。
As shown in Figure 2, [5i02 (%) in 0.25 mm]
Both RDI and product yield are improved with an increase in S i 02 (%) in -0,25r ILTIL.
.. 85 or higher, the RDI and product yield are significantly improved.As shown in Figures 1 and 2, the RDI of sintered ore,
In order to maintain a good product yield, -0.2
[Al2O3/SiO□] in 5rItm should be 0.25 or less, and 5in2 (%) in -0.25van should be 0.25 or less.
It can be seen that it is important to set the score to 85 or higher.

−0,25mm中(A407S i02]を0.25以
下とし、かツー 0.25 rILm中5iO2(%)
を0.85以上とするためにはS i 02源として添
加する原料例えば砂石を微粉砕すること、Al2O3含
有量の大きな鉱石の微破砕を遮けることによって調整す
るのが有効である。
- 0.25 mm (A407S i02) or less, 5iO2 (%) in 0.25 rILm
In order to make the value 0.85 or more, it is effective to adjust it by finely pulverizing the raw material added as the S i 02 source, such as sand stone, or by preventing the fine crushing of ores with a large Al2O3 content.

このように配合原料中−0,25mm未満の微粉部分に
含まれるSiO3の量とAl2O3/S i 02を調
整することによって配合原料中の粒径1mm以上の粗粒
部分のAl2O3含有量を大きくし得るので焼結鉱のA
l2O3含有量は従来2.0%以上は好ましくないとさ
れていたものをAl2O3を3.3%程度含有する高A
l2O3含有鉱石を60%以上配合して焼結鉱のAl2
O3含有量を2.0%超とすることが可能である。
In this way, by adjusting the amount of SiO3 and Al2O3/S i 02 contained in the fine powder part with a particle size of less than -0.25 mm in the mixed raw material, the Al2O3 content in the coarse part with a particle size of 1 mm or more in the mixed raw material can be increased. A of sintered ore is obtained.
A high A content containing about 3.3% Al2O3, which was conventionally considered undesirable with an Al2O3 content of 2.0% or more,
Al2 of sintered ore by blending 60% or more of l2O3-containing ore
It is possible to have an O3 content of more than 2.0%.

焼結鉱のAl2O3含有量は配合原料のA403含有量
によって決まる。
The Al2O3 content of the sintered ore is determined by the A403 content of the blended raw materials.

一般に配合原料を焼結すること1こよりAl2O3は約
1.1倍に濃縮するので、この濃縮度合を考慮して配合
原料の段階で焼結鉱のAl2O3含有量を求めることが
でき以後この値を焼結鉱に換算したAl2O3含有量と
呼ぶことにする。
Generally, Al2O3 is concentrated approximately 1.1 times by sintering the blended raw materials, so taking this concentration degree into account, the Al2O3 content of the sintered ore can be determined at the stage of blending raw materials, and this value can be used thereafter. This will be referred to as the Al2O3 content converted to sintered ore.

また、配合原料の粒度1こついてであるが、通常の配合
原料は例えば第7表に示すように粒度分布をもっており
、このうち粒径1mm未満の細粒部分の重量割合は通常
25〜60%の範囲内にある。
In addition, although the particle size of the blended raw materials is 1, ordinary blended raw materials have a particle size distribution as shown in Table 7, of which the weight proportion of fine particles with a particle size of less than 1 mm is usually 25 to 60%. is within the range of

この値が25%より少ない場合は焼結に際してボンドの
形成が不十分となり焼結鉱の強度を維持することができ
なくなる。
If this value is less than 25%, bond formation will be insufficient during sintering, making it impossible to maintain the strength of the sintered ore.

また、この値が60%を超えると焼結時の通′気性を悪
化させるという問題が生じるので造粒を強化するなどの
対策を必要とする。
Furthermore, if this value exceeds 60%, a problem arises in that the air permeability during sintering is deteriorated, so countermeasures such as strengthening the granulation are required.

本発明においては前記焼結鉱の強度維持及び焼結時の通
気性の観点から粒径1rILm未満の細粒部分を25%
以上含むもので望ましくは25%以上60%以下の粒度
分布を有する配合原料を使用する。
In the present invention, from the viewpoint of maintaining the strength of the sintered ore and breathability during sintering, the fine grain portion with a grain size of less than 1rILm is reduced to 25%.
A compounding raw material containing the above, preferably having a particle size distribution of 25% or more and 60% or less is used.

実施例 鉄鉱石、石灰石、砂石、コークス及び返鉱を混合した配
合原料に水を加えて造粒し、それを40ゆ試験鍋にて負
圧1700 朋H20で焼結鉱を製造した。
Example Water was added to a mixed raw material of iron ore, limestone, sandstone, coke and return ore to granulate it, and the sintered ore was produced using a negative pressure of 1700 mm in a 40 mm test pot.

配合原料となる鉱石、砂石、石灰石、ジュナイト、返鉱
、コークスの組成を第1表〜第4表に示した。
Tables 1 to 4 show the compositions of ore, sandstone, limestone, juite, return ore, and coke, which are the raw materials to be blended.

配合割合は比較例を含めて第5表に示し、試験条件を第
6表に、配合原料の粒度分布を第7表に示した。
The blending ratios, including comparative examples, are shown in Table 5, the test conditions are shown in Table 6, and the particle size distribution of the blended raw materials is shown in Table 7.

また、−0,25mm中〔Al2O3/5i02)及び
−0,25rnm中5iO2(%)を比較例を含めて、
第8表に示した。
In addition, [Al2O3/5i02] in -0,25 mm and 5iO2 (%) in -0,25 nm, including comparative examples,
It is shown in Table 8.

比較例1の配合原料は第1表及び第5表に示すようにA
l2O3含有量の小さい鉄鉱石Cを37,2%とAl2
O3含有率の大きい鉄鉱石りを26.7%配合し、かつ
該鉄鉱石りは破砕したので−0,25mm中(A403
/S i 02]は0.36と高く、砂石の配合率は2
.0重量%て−0.25麿中S i 02 (% )は
0.96、焼結鉱に換算したAl2O3含有率は2.0
重量%とした。
The raw materials for Comparative Example 1 were A as shown in Tables 1 and 5.
37.2% iron ore C with low l2O3 content and Al2
Since 26.7% of iron ore with a high O3 content was blended, and the iron ore was crushed, -0.25 mm (A403
/S i 02] is as high as 0.36, and the blending ratio of sandstone is 2.
.. 0 wt% -0.25 Maronaka Si02 (%) is 0.96, Al2O3 content converted to sintered ore is 2.0
It was expressed as weight%.

比較例2の配合原料は鉱石の配合割合を比較例1とほぼ
同じとし、砂石配合率を1.8重量%1こ低減し、Al
2O3含有率の大きい鉄鉱石Aの一部を破砕し、かつ破
砕した鉄鉱石りを51.7%配合したものであって、−
〇、25WtrIL中S i 02 (%)は0.93
、焼結鉱に換算したAl2O3含有率は2.6重量%と
高くまた−0.25rnm中〔Al2O3/SiO2〕
は0.49と高い値になっている。
The blended raw materials of Comparative Example 2 had the ore blending ratio almost the same as Comparative Example 1, the sandstone blending ratio was reduced by 1.8% by weight, and the Al
A part of iron ore A with a high 2O3 content is crushed and 51.7% of the crushed iron ore is blended, -
〇, S i 02 (%) in 25WtrIL is 0.93
, the Al2O3 content converted to sintered ore is as high as 2.6% by weight, and in -0.25rnm [Al2O3/SiO2]
has a high value of 0.49.

これをこ対し、実施例1の配合原料は鉱石の配合割合を
比較例1と同じとし、Al2O3含有率、の大きい鉄鉱
石りを粗粒で配合し、かつ砂石の配合割合を2.0重量
%にしたもので焼結鉱に換算した。
On the other hand, the blended raw materials of Example 1 have the same proportion of ore as Comparative Example 1, contain coarse particles of iron ore with a high Al2O3 content, and have a blended proportion of sand and stone of 2.0. It was converted to sintered ore in weight percent.

Al2O3含有率は2.0重量%で比較例1と同等であ
るが−0,25mm中〔Al2O3/SiO2〕は0.
23と1成域されており、−025rnrIL中S A
02 (%)は0.95実施例2の配合原料は、−石の
配合割合を比較例2のものと同等とし、砂石、シュナイ
ト、Al2O3の低い鉄鉱石Cの一部を0.25wLr
IL未満(こ微粉砕し、Al2O3含有量の高い鉱石を
粗粒で配合したもので、焼結鉱に換算したAl2O3含
有率は2.6重量%で比較例2と同等であるが、−〇、
25rn7IL中〔Al2O3/5i02〕は0.20
と低く、−0,25mm中S i 02 (%)は0.
85に維持した。
The Al2O3 content is 2.0% by weight, which is the same as in Comparative Example 1, but the [Al2O3/SiO2] in -0.25 mm is 0.
23 and 1 area, and S A in -025rnrIL
02 (%) is 0.95 The blended raw materials of Example 2 are as follows.
Less than IL (this is a mixture of finely pulverized ore with high Al2O3 content in coarse particles, and the Al2O3 content converted to sintered ore is 2.6% by weight, which is the same as Comparative Example 2, but -〇 ,
[Al2O3/5i02] in 25rn7IL is 0.20
The S i 02 (%) at -0.25 mm is as low as 0.
It was maintained at 85.

なお、焼結鉱の5i02は比較例、実施例とも5.6%
とした。
In addition, 5i02 of sintered ore is 5.6% in both the comparative example and the example.
And so.

このような配合原料を焼結した結果を第9表にまとめて
示すと共にグラフ化して第3図に示した。
The results of sintering such blended raw materials are summarized in Table 9 and are shown in a graph in FIG.

第9表及び第3図に示すようをこ、現在普通に用いられ
ている配合原料を焼結した比較例1及び高Al2O3原
料を多配合した比較例2では−0,25rnrrt中〔
Al2O3/5i02〕を0.25以下にすることがで
きずに、RDI及び成品歩留は悪化傾向を示し、また落
下強度、コークス原単位も同様な傾向を示した。
As shown in Table 9 and FIG. 3, in Comparative Example 1, in which blended raw materials commonly used at present were sintered, and in Comparative Example 2, in which a large number of high Al2O3 raw materials were blended, -0.25 rnrrt was used.
[Al2O3/5i02] could not be reduced to 0.25 or less, and the RDI and product yield showed a deteriorating trend, and the falling strength and coke consumption showed a similar trend.

これに対し−0,25Inrn中(A 1j207S
i 02)を0.23に抑えると共に−0,25rnr
n中S i、 0si(%)を0.95に維持した実施
例1では焼結鉱のS i 02含有量を5.6電量診と
し、焼結鉱に換算したAl2O3含有量を2.0′N量
%と比較例↓と同等にしたtこもかかわらずRDI及び
成品歩留が向上し、焼結時間の延長や生産率の低下を伴
わずにコークス原単位及び落下強度を改善できた。
On the other hand, in -0,25Inrn (A 1j207S
i 02) to 0.23 and -0.25rnr
In Example 1, in which Si, 0si (%) in n was maintained at 0.95, the S i 02 content of the sintered ore was set to 5.6 coulometric test, and the Al2O3 content converted to the sintered ore was set to 2.0. Even though the N amount% was made the same as that of the comparative example↓, the RDI and product yield were improved, and the coke consumption rate and falling strength were improved without extending the sintering time or decreasing the production rate.

また、−0,25mm中〔Al2O3/SiO□〕を0
.20と低減させ−0,25rILrIL中5i92(
:%)を0.85とした実施例2では焼結鉱に換算した
Al2O3を2.6重量%としたにもかかわらずれD■
、成品歩留、落下強度はもとより焼結時間、生産率、コ
ークス原単位を実施例1と回廊の値とすることができた
Also, in -0,25mm [Al2O3/SiO□] is 0
.. 20-5i92 in 0,25rILrIL(
:%) was 0.85 and the Al2O3 content was 2.6% by weight in terms of sintered ore.
, product yield, and falling strength as well as sintering time, production rate, and coke consumption were able to match the values of Example 1 and Corridor.

以上述べたように本発明によれば生産性、コークス原単
位、落下強度などを従来と同等ないしは、それ以上のレ
ベルに保持しながら、低温還元粉化指数を悪化させるこ
となく焼結鉱のAl2O3を2.0重量%超とすること
ができる。
As described above, according to the present invention, the Al2O3 of sintered ore is maintained without deteriorating the low-temperature reduction powdering index while maintaining productivity, coke consumption, falling strength, etc. at the same or higher level than conventional ones. can be more than 2.0% by weight.

すなわち従来約2.0%を上限として焼結鉱のAl2O
3は管理されてきたが、本発明法によれば、2.0%超
とすることが可能であり、たとえ焼結鉱の平均値におい
て高Al2O3だとしても微粉部分のAl2O3を下げ
ることによって焼結鉱品質の良い焼結鉱の製造が可能で
あり、従来の品質維持を前提とするならば高Al2O3
鉱石の高配合が可能となって、配合の自由度が広がり、
焼結操業上重要な利AφS得られる。
That is, the Al2O content of sintered ore was conventionally set at about 2.0% as an upper limit.
However, according to the method of the present invention, it is possible to increase the Al2O3 content to over 2.0%. It is possible to produce sintered ore with good concretion quality, and if the conventional quality is maintained, high Al2O3 is possible.
It becomes possible to mix ores at a high level, increasing the degree of freedom in mixing.
Gain AφS, which is important for sintering operations, can be obtained.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は460mDL焼結機データから得た焼結鉱配合
原料の0.25 vtw未満微粉部分のA7203/S
iO2重量比と焼結鉱の低温還元粉化指数、成品歩留の
関係を示す図、第2図は40kg試験鍋焼成データから
得た焼結鉱配合原料の0.25 rItm未満微粉部分
のS i 02重量%と焼結鉱の低温還元粉化指数、成
品歩留の関係を示す図、第3図は本発明の実施例につい
て、平均Al2O3量イ、0.25 WLm未満;微粉
部分のA/l!20s/ S i 02重量比口、低温
還元粉化指数ハ、成品歩留二、焼結時間ホ、生産率へ、
コークス原単位ト、落下強度チを表わす各図である。
Figure 1 shows A7203/S of the fine powder portion of less than 0.25 vtw of the sintered ore blend raw material obtained from the 460mDL sintering machine data.
Figure 2 shows the relationship between the iO2 weight ratio, the low-temperature reduction pulverization index of sintered ore, and the product yield. Figure 3 shows the relationship between i02% by weight, the low-temperature reduction powdering index of sintered ore, and the product yield. /l! 20s/S i 02 weight ratio, low temperature reduction powdering index c, product yield 2, sintering time e, production rate,
FIG. 3 is a graph showing coke consumption rate and falling strength.

Claims (1)

【特許請求の範囲】 1 粒径1韮未満の細粒部分を25重量%以上含有する
配合原料において、該配合原料中粒径0.25mm未満
の微粉部分に含まれる5i02量を配合原料を構成する
成分全体の0.85重量%以上とすると共に該微粉部分
のAl2O3/5i02重量比を0.25以下に調整し
、このよう【こ調整した配合原料を焼結することを特徴
とする高Al2O3含有鉱石の高配合を可能とした焼結
鉱の製造方法。
[Scope of Claims] 1. In a blended raw material containing 25% by weight or more of a fine part with a particle size of less than 1 mm, the amount of 5i02 contained in the fine part with a particle diameter of less than 0.25 mm in the blended raw material constitutes the blended raw material. High Al2O3 is characterized by adjusting the Al2O3/5i02 weight ratio of the fine powder part to 0.25 or less and sintering the blended raw materials adjusted in this way. A method for producing sintered ore that allows for a high content of ore.
JP5070180A 1980-04-17 1980-04-17 A method for producing sintered ore that enables high blending of ores containing high Al↓2O↓3 Expired JPS5818413B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5070180A JPS5818413B2 (en) 1980-04-17 1980-04-17 A method for producing sintered ore that enables high blending of ores containing high Al↓2O↓3

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5070180A JPS5818413B2 (en) 1980-04-17 1980-04-17 A method for producing sintered ore that enables high blending of ores containing high Al↓2O↓3

Publications (2)

Publication Number Publication Date
JPS56146832A JPS56146832A (en) 1981-11-14
JPS5818413B2 true JPS5818413B2 (en) 1983-04-13

Family

ID=12866198

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5070180A Expired JPS5818413B2 (en) 1980-04-17 1980-04-17 A method for producing sintered ore that enables high blending of ores containing high Al↓2O↓3

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Country Link
JP (1) JPS5818413B2 (en)

Also Published As

Publication number Publication date
JPS56146832A (en) 1981-11-14

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