JPS5935969B2 - Method for manufacturing sintered ore - Google Patents
Method for manufacturing sintered oreInfo
- Publication number
- JPS5935969B2 JPS5935969B2 JP13833181A JP13833181A JPS5935969B2 JP S5935969 B2 JPS5935969 B2 JP S5935969B2 JP 13833181 A JP13833181 A JP 13833181A JP 13833181 A JP13833181 A JP 13833181A JP S5935969 B2 JPS5935969 B2 JP S5935969B2
- Authority
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- Japan
- Prior art keywords
- sintered ore
- amount
- slag
- ore
- feo
- 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
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Description
【発明の詳細な説明】
本発明は焼結鉱の製造方法に係り、オリビン系スラグボ
ンドを強化して焼結鉱中の脈石量(SiO3量)低減を
可能ならしめ、その高温性状の改善および高炉スラグ比
の低減により高炉燃料比低減と銑中Siの低減を図り得
る硬質の焼結鉱を製造することのできる方法を得ようと
するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing sintered ore, which strengthens olivine-based slag bonds to reduce the amount of gangue (SiO3 amount) in sintered ore, and improves its high-temperature properties. Another object of the present invention is to obtain a method for producing hard sintered ore that can reduce the blast furnace fuel ratio and the Si content in the pig iron by reducing the blast furnace slag ratio.
トロイドロイド式のような焼結機における焼結過程は配
合原料を構成する鉄鉱石、雑原料、造滓剤およびコーク
スなどを混合すると共に水分を添加し造粒した後焼結機
に装入し、点火炉で原料表層部に点火して下向きに空気
を吸引せしめることにより原料中のコークスを燃焼させ
、その発熱により原料粒子相互の焼結反応ないし溶融(
半溶融)反応を図り、これを冷却することにより気孔率
が高く、原料の鉄鉱石とは全く異った鉱物組成を形成す
る。The sintering process in a sintering machine such as the toroidroid type involves mixing the raw materials such as iron ore, miscellaneous raw materials, slag forming agents, coke, etc., adding moisture, granulating the material, and then charging it into the sintering machine. By igniting the surface layer of the raw material in an ignition furnace and sucking air downward, the coke in the raw material is burned, and the heat generated causes a sintering reaction or melting of the raw material particles (
By attempting a semi-molten) reaction and cooling it, a mineral composition with high porosity and completely different from that of the raw iron ore is formed.
このような焼結操業の目標は品質基準を満足し、生産性
を向上し、コークス原単位を低下することの3点である
から通常は焼結鉱の品質が維持できる範囲内で生産性を
向上させ且つコークス原単位を低減させるような操業が
指向されている。The goals of such sintering operations are to satisfy quality standards, improve productivity, and reduce coke consumption, so productivity is usually maintained within the range that maintains the quality of the sintered ore. Operations are aimed at improving coke consumption and reducing coke consumption.
ところで焼結鉱に要求される性状としては強度、耐還元
粉化性、被還元性、高温性状などが考えられるが、これ
らの各性状を共に満足せしめようとする場合において、
それぞれの性状を満足させるための条件が相反する場合
が多(、例えば500〜600℃の温度範囲での還元雰
囲気における粉化を避ける耐還元粉化性を改善するため
にはコークス比の増加や脈石量の増加などが有効である
が、これらのアクションは反面において被還元性やコー
クス比の悪化を来し、又高炉燃料比の増加を招くという
不利を伴う。By the way, properties required for sintered ore include strength, resistance to reduction and pulverization, reducibility, high temperature properties, etc., but when trying to satisfy all of these properties,
In many cases, the conditions for satisfying each property are contradictory (e.g., to avoid powdering in a reducing atmosphere in the temperature range of 500 to 600°C, and to improve resistance to reduction powdering, it is necessary to increase the coke ratio or Although increasing the amount of gangue is effective, these actions have the disadvantage of deteriorating the reducibility and coke ratio and increasing the blast furnace fuel ratio.
従って実操業においては上記したように要求される諸性
状に優先順位を設け、その管理限界内での最大の生産を
得るよ5Kt、て操業している。Therefore, in actual operation, priority is given to the required properties as described above, and the plant is operated at 5Kt in order to obtain the maximum production within the control limits.
然して近時における高炉装入原料の高温性状(高温での
被還元性、軟化溶融特性およびそれらによる通気性の変
化)K関するより正確な測定、評価を目的とした荷重軟
化溶融試験の結果として、焼結鉱の高温性状に差をもた
らしている原因は、直接的にはスラグの同化反応過程に
おける融液生成量の大小、間接的には1000℃以上の
高温での被還元性および還元前の脈石組成と量であるこ
とが判明し、これらの中でも特に焼結鉱の脈石量の低減
(CaO/SiO□)−量の低減)は高温性状を大きく
改善させ、高炉でのスラグ量低減と共に高炉燃料比を大
幅に低減させ得ることが確認された。However, as a result of recent load softening and melting tests aimed at more accurate measurement and evaluation of the high temperature properties (reducibility, softening and melting characteristics at high temperatures, and changes in air permeability due to these) of blast furnace charging raw materials, The causes of differences in the high-temperature properties of sintered ore are directly due to the amount of melt produced during the slag assimilation reaction process, and indirectly due to the reducibility at high temperatures of 1000°C or higher and the temperature before reduction. It was found that the gangue composition and amount are particularly important, and among these, the reduction in the amount of gangue in sintered ore (CaO / SiO It was also confirmed that the blast furnace fuel ratio could be significantly reduced.
しかし斯様にして焼結鉱の脈石量を低減させたSiO2
が5.2係以下のような低5i02の焼結鉱は高炉内の
400〜600℃の温度域における還元雰囲気で粉化さ
れ易く、現在の品質管理項目の1つである還元粉化指数
(RDI : 550℃、30分の還元雰囲気で保持し
た焼結鉱をドラム中で900回転後の一3mmの重量割
合)が大きく悪化し、且つ焼結時間が長くなって生産率
の低下、又は生産率を一定に保った場合の歩留および強
度(si)が低下するという不利がある。However, SiO2 which reduced the amount of gangue in sintered ore in this way
Sintered ore with a low 5i02 coefficient of 5.2 or less is easily pulverized in the reducing atmosphere in the temperature range of 400 to 600°C in a blast furnace, and the reduction pulverization index ( RDI: After 900 rotations of sintered ore held in a reducing atmosphere at 550°C for 30 minutes, the weight ratio of 13 mm (weight ratio) deteriorates significantly, and the sintering time becomes longer, resulting in a decrease in production rate or production The disadvantage is that the yield and strength (si) are reduced when the ratio is kept constant.
なおこの低SiO□焼結鉱の製造に関しては田代氏等に
より若干の提案が重ねられてはいるが、これらのものは
Sio2源を粉砕することにより1間未満の微粉部分に
おけるSiO□量を増加せしめ、この微粉部分のCab
/Sin□又&j−CaO/ (S 102−Ae20
3)をあるノベル以下にし、或いは該微粉部分を55多
以上となし、又このように微粉調整したものの原料予熱
を併用するものであって、要するに低SiO2化に伴っ
て予想されるシリケートスラグボンド生成量の減少をそ
の5i02源を粉砕し、有効SiO□量を増大せしめる
ことによって補償しようとするものである。Regarding the production of this low-SiO□ sintered ore, there have been several proposals by Mr. Tashiro et al., but these proposals involve increasing the amount of SiO□ in the fine powder portion of less than 1 min by pulverizing the SiO2 source. Seshime, this fine powder part Cab
/Sin□mata&j-CaO/ (S 102-Ae20
3) is made below a certain level, or the fine powder portion is made more than 55, and the raw material preheating of the finely adjusted powder is also used, in short, the silicate slag bond expected with the reduction of SiO2. The aim is to compensate for the decrease in production by pulverizing the 5i02 source and increasing the effective amount of SiO□.
しかしこのようKして低SiO2化を図ったとしてもボ
ンドとしてシリケートスラグを使用する以上は限度があ
り、従って焼結鉱に好ましい低S i02化を得るには
配合する鉱石の銘柄について相当の選択をしなければな
らないことになり、又そのような意味から長期的に継続
することは不可能であって安定した低5i02化操業を
継続することが困難である。However, even if low SiO2 is achieved by using K, there is a limit as long as silicate slag is used as a bond.Therefore, in order to obtain a desirable low SiO2 for sintered ore, considerable selection must be made regarding the brand of ore to be blended. In addition, from this point of view, it is impossible to continue for a long period of time, and it is difficult to continue stable low 5i02 operation.
本発明は上記したような実情に鑑み検討を重ねて創案さ
れたものであって、FeOを6係以上名有した鉱石又は
スケール、噴出滓、転炉滓、篩下滓、ダスト類のような
雑原料の一部又は全部を粉砕して粒度調整し、1朋未満
の微粉部分におけるFed/5in2を0.8〜2.3
となるように調整することを提案するものであり、又こ
のような調整と共に焼結鉱の5i02a有量を4.6〜
5.4となるように配合原料のS i02含有量を調整
することを提案するものである。The present invention was created after repeated studies in view of the above-mentioned circumstances, and is intended to be applied to ores containing 6 or more FeO, such as scales, eruption slag, converter slag, sieve slag, and dust. Part or all of the miscellaneous raw materials are pulverized to adjust the particle size, and the Fed/5in2 in the fine powder part of less than 1 tom is 0.8 to 2.3.
It is proposed that the amount of 5i02a in the sintered ore should be adjusted to 4.6 to 4.6.
It is proposed to adjust the S i02 content of the blended raw materials so that it becomes 5.4.
即ち上記のようにして微粉部分中のFed/5in2を
高めに制御することにより、従来のシリケート系スラグ
ボンドに加えてオリビン系スラグボンドの生成を促進強
化して好ましい焼結鉱を得しめることができ、生産性や
コークス原単位を悪化させずに還元粉化指数(RDI)
や冷間強度(SI)を適切に得しめ、しかも焼結鉱中の
脈石量(Si02量)低減を可能ならしめる。That is, by controlling Fed/5in2 in the fine powder portion to a high value as described above, it is possible to promote and strengthen the formation of olivine-based slag bonds in addition to the conventional silicate-based slag bonds, thereby obtaining a preferable sintered ore. reduction index (RDI) without deteriorating productivity or coke consumption rate.
This makes it possible to obtain appropriate cold strength (SI) and to reduce the amount of gangue (Si02 amount) in the sintered ore.
又斯かる本発明につ(・て更に説明すると、自溶性焼結
鉱の焼結反応は固相反応としての拡散結合は少(、大部
分は溶融相を介しての結合であるので融液Q果す役割が
極めて重要である。In addition, regarding the present invention, to explain further, in the sintering reaction of self-fusing sintered ore, there is little diffusion bonding as a solid phase reaction (but most of the bonding is through the molten phase, so there is no molten liquid Q: The role it plays is extremely important.
又その平衡的組織は酸化鉄粒子なスラグが結合する所謂
溶融結合型であり、このスラグボンドにより焼結鉱の品
質、生産性が大きく左右される。The equilibrium structure is a so-called fusion bond type in which slag particles such as iron oxide particles are bonded, and the quality and productivity of the sintered ore are greatly influenced by this slag bond.
しかしドワイトロイド式焼結機を使用した現状のプロセ
スでは高温での反応時間が極めて短(、しかも完全溶融
状態になるまで加熱されないので部分的に生成した融液
を介して結合が進んで行くため如何にして脈石を迅速且
つ均一にスラグ化し生成せしめるかが重要な課題である
。However, in the current process using a Dwight Lloyd sintering machine, the reaction time at high temperatures is extremely short (and since the heating is not completed until it reaches a completely molten state, bonding proceeds through the partially formed melt). An important issue is how to quickly and uniformly convert gangue into slag.
特に脈石量を少(して低SiO□の焼結鉱を製造する場
合にはこのことが極めて重要であり、脈石量、即ち造滓
量の減少な造滓源の有効率を高めるなど何等かの手段で
補償することが必要である。This is especially important when manufacturing sintered ore with low SiO□ with a small amount of gangue. It is necessary to compensate by some means.
ところで焼結は種々の化学組成の混合粉体の内、融液の
生成し易1粒子の組合わせ(低融点の化学組成領域に相
当する粒子の組合わせ)のところから、融液が生成し、
昇温に従ってその量が増加し且つ拡がり、融液間の反応
および合体を通じて結合が進むものと推定されるが、上
記のように高温での滞留時間が短い場合には粗粒原料又
は滓化性の劣った原料は完全に溶融しないで未反応のま
ま残留することが多い。By the way, in sintering, a melt is generated from a combination of particles that are likely to generate a melt (a combination of particles corresponding to a chemical composition region with a low melting point) among mixed powders with various chemical compositions. ,
It is assumed that the amount increases and spreads as the temperature rises, and that the bonding progresses through reactions and coalescence between the melts, but if the residence time at high temperatures is short as described above, coarse grain raw materials or slag formation will occur. Inferior raw materials often remain unreacted without being completely melted.
本発明者等はこれらの点について仔細に検討し実験を重
ねた結果、FeOを6チ以上自有するよ5なFeOの高
い鉱石又は前記したような雑原料を粉砕してINN未満
の微粉部分におけるF e O/S i O□を0.8
〜2.3となるように粒度調整して使用することが生産
性およびコークス原単位を適切に確保して前記した還元
粉化指数(RDI)や冷間強度(SI)を改善する上で
のキーポイントであり、あるいは又このRDI値やSI
値を確保しながら焼結鉱中脈石量(SiO□量)を低減
するキーポイントたることを確認した。As a result of careful consideration and repeated experiments on these points, the present inventors have found that by pulverizing ores with high FeO content of 6 or more or the above-mentioned miscellaneous raw materials, a fine powder portion of less than INN is obtained. F e O/S i O □ at 0.8
Adjusting the particle size to ~2.3 is the best way to ensure productivity and coke consumption appropriately, and improve the reduction index (RDI) and cold strength (SI) mentioned above. This is a key point, or also this RDI value or SI
It was confirmed that this is a key point in reducing the amount of gangue (SiO□ amount) in sintered ore while maintaining the same value.
ところで焼結原料は一途的にその混合造粒過程において
、第1図に示すよ5VC1〜5關の粗粒を核とし、その
周囲KO,5〜未満の微粉を耐着した擬似粒子を形成し
、スラグ融液の生成はこの附着した微粉原料を起点とし
て始まり、次第に周りの粗粒原料を溶かし込んで焼結が
進行するため還元粉化性および冷間強度を改善するには
このスラグ融液を迅速に生成し又成る程度以上生成させ
ることが必要である。By the way, during the mixing and granulation process of the sintered raw material, as shown in Fig. 1, pseudo-particles are formed with coarse grains of 5VC1 to 5 as cores and fine particles of less than KO, 5 or more adhering to the surroundings. The generation of slag melt starts from this attached fine powder raw material, and sintering progresses by gradually dissolving the surrounding coarse grain raw material, so this slag melt is necessary to improve reduction powdering properties and cold strength. It is necessary to rapidly produce and to produce to a certain extent.
第2図にFeQ−8102−CaO系の1150℃以下
の低融点領域をDとして示したが、FeOの高い鉱石や
上記のような雑原料が粉砕されてスラグ融液の起点とな
る1mrIL未満の微粉部分におけるFeO/S i0
2を0.8〜2.3 K制御し、オリビン系(CaO5
102Fed)スラグを迅速に生成し易くすることによ
り生産性、コークス原単位を劣化することな(、耐還元
粉化性および冷間強度の優れた焼結鉱を製造することが
可能となる。In Figure 2, the low melting point region below 1150°C of the FeQ-8102-CaO system is shown as D. FeO/S i0 in the fine powder part
2 was controlled at 0.8 to 2.3 K, and olivine-based (CaO5
102Fed) By making it easier to quickly generate slag, it is possible to produce sintered ore with excellent reduction powdering resistance and cold strength without deteriorating productivity and coke consumption.
又還元粉化性、冷間強度を劣化させない範囲で脈石量の
低減も可能となる。Furthermore, it is possible to reduce the amount of gangue within a range that does not deteriorate reduction powdering properties and cold strength.
つまり脈石量(SiO2量)を減らしても従来のシリケ
ート系スラグボンドに加えてオリビン系スラグボンドが
有効に生成するため生産性、コークス原単位および品質
を劣化することなしに脈石量の低減が可能となり、それ
に伴って高温性状の改善および高炉スラグ比の低減によ
る高炉燃料比の低減と銑鉄中Siの低減を得しめる。In other words, even if the amount of gangue (SiO2 amount) is reduced, olivine-based slag bond is effectively generated in addition to the conventional silicate-based slag bond, so the amount of gangue can be reduced without deteriorating productivity, coke consumption, or quality. This makes it possible to improve high-temperature properties, reduce the blast furnace fuel ratio by reducing the blast furnace slag ratio, and reduce Si in the pig iron.
本発明によるものの具体的な実施例を比較のための従来
例および参考例と共に示すと以下の如くである。Specific examples according to the present invention are shown below together with conventional examples and reference examples for comparison.
実施例 1
次の銘柄の鉄鉱石と石灰石、ドロマイト、ケイ石、コー
クス、返鉱などを準備し、これらを用いた従来例1によ
るものは次の第1表に示す通りである。Example 1 The following brands of iron ore, limestone, dolomite, silica stone, coke, return ore, etc. were prepared, and conventional example 1 using these materials is as shown in Table 1 below.
−1mm5iQ2== 2.58
−17n?+!FeO−= 1.57
−1 mmFeo/S i02 = 0.61この第1
表に示すものを通常の方法で5i02源を低減したSi
O2:5゜4チの配合とした参考例1は次の第2表に示
す通りである。-1mm5iQ2== 2.58 -17n? +! FeO−= 1.57 −1 mmFeo/S i02 = 0.61 this first
What is shown in the table is Si with reduced 5i02 source using the usual method.
Reference Example 1 with a blend of O2: 5°4 is as shown in Table 2 below.
一11m5iO□=2.35
−1 mmFe0= 1.57
1 mmF eo/S to 2 =、0.67これら
のものに対し本発明によるものの具体的な配合例は次の
第3表に示す通りであって、FeOの高い鉱石又は雑原
料の一部又は全部を粉砕して粒度調整し、111Lm未
満の微粉部分のFeO/SiO2を0.8〜2,3の範
囲内である0、95に調整し、同に焼結鉱中のSiO□
量を低減させるため、ケイ石、蛇紋岩をカットしてドロ
マイト、石灰石の配合を調整したものである。−11m5iO□=2.35 −1 mmFe0=1.57 1 mmFeo/S to 2 =, 0.67 Contrary to these, specific formulation examples of the products according to the present invention are as shown in Table 3 below. Then, part or all of the ore or miscellaneous raw material with high FeO is pulverized to adjust the particle size, and the FeO/SiO2 of the fine powder portion less than 111 Lm is adjusted to 0.95, which is within the range of 0.8 to 2.3. However, SiO□ in the sintered ore
In order to reduce the amount, silica stone and serpentine are cut and the blend of dolomite and limestone is adjusted.
−1關SiO□−2,46
一1mmFe0 :=2.34
1 mmF eO/S t02 = O−95これら第
1〜第3表に示した配合原料は夫々水を添加して造粒し
、又これらを何れも50ky試験鍋によって負圧130
0m’1lAqで吸引し、鍋焼給鉱を製造した。-1 關SiO□-2,46 -1 mmFe0 :=2.34 1 mmF eO/S t02 = O-95 These compounded raw materials shown in Tables 1 to 3 were granulated by adding water, and Negative pressure 130
The suction was carried out at 0 m'11 Aq to produce pot sintered ore.
得られた各焼結鉱についての生産率、強度、成品歩留、
還元粉化率(RDI)およびRI値を示すと次の第4表
の通りである。Production rate, strength, product yield, and
The reduction ratio (RDI) and RI value are shown in Table 4 below.
即ち従来例1・、のものに対し参考例1のものはそのS
iO□量の低減に伴い、生産率、強度、成品歩留および
RDIが悪化し、その焼結操業および焼結鉱性状が大き
く劣化する。In other words, compared to Conventional Example 1, Reference Example 1 has its S
As the amount of iO□ decreases, the production rate, strength, product yield, and RDI deteriorate, and the sintering operation and properties of the sintered ore greatly deteriorate.
これらのものに対し上記のようVC1mm未満の微粉成
分のF e O/S t O2を0.95に調整した本
発明の実施例1のものは生産率を悪化しないで強度、成
品歩留、RDIおよびRIをそれぞれに改善することが
できた。In contrast to these products, the product of Example 1 of the present invention, in which the F e O/S t O2 of the fine powder component with a VC of less than 1 mm was adjusted to 0.95, has improved strength, product yield, and RDI without deteriorating the production rate. and RI could be improved respectively.
実施例 2
蛇紋岩をも使用した従来例2の配合は次の第5表に示す
通りである。Example 2 The formulation of Conventional Example 2, which also used serpentine, is as shown in Table 5 below.
−1xis i02 == 2.42
−1 mmFe0 = 1.59
1 mm F e O/St 02 =0.66又これ
を常法によりS i02量を低減させ、低5i02焼結
鉱を製造するよ5Kした参考例2のものは次の第6表に
示すような配合になる。-1xis i02 == 2.42 -1 mmFe0 = 1.59 1 mm F e O/St 02 =0.66 Then, the amount of Si02 is reduced by a conventional method to produce a low 5i02 sintered ore. The composition of Reference Example 2 was as shown in Table 6 below.
−1m5i02=2.04
−1 m1FeO= 1.51
−1m1Feo/5i02=0.74
更に本発明に従い、実施例1の場合におけると同様にF
eOの窩い鉱石又は雑原料を粉砕して1間未満の微粉部
分のFeO,/5i02を本発明範囲内・の1.09と
し、しかもケイ石や蛇紋岩をカットしてドロマイト、石
灰を用いて配合を調整した本発明実施例2の配合は次の
第7表に示す通りである。−1m5i02=2.04 −1 m1FeO=1.51 −1m1Feo/5i02=0.74 Furthermore, according to the invention, F
By pulverizing eO ore or miscellaneous raw materials, the FeO,/5i02 of the fine powder part of less than 1 min is within the scope of the present invention and 1.09, and in addition, dolomite and lime are used by cutting silica and serpentinite. The formulation of Example 2 of the present invention, in which the formulation was adjusted, is as shown in Table 7 below.
−1mm 5in2= 2.14
−1 mrnFeO= 2.34
1 mmF eO/S t 02 =1.09然してこ
れら第5〜7表に示す各配合のものについて実施例IV
Cおけると同様に焼結鉱を製造し、その生産率、強度、
成品歩留りな≧を測定した結果を要約して示すと次の第
8表の通りであり、実、く施例IKついて述べた同様に
参考列2のものは生産率、強度、成品歩留及びRDIが
悪化しているのに対し、本発明の実施例2によるものは
それらを大幅に改善することが確認された。-1 mm 5in2 = 2.14 -1 mrnFeO = 2.34 1 mmF eO/S t 02 = 1.09 For each of the formulations shown in Tables 5 to 7, Example IV
Sintered ore is manufactured in the same manner as in C, and its production rate, strength,
The results of measuring product yield ≧ are summarized as shown in Table 8 below, and in the same way as described for Example IK, reference column 2 shows the production rate, strength, product yield and It was confirmed that while the RDI deteriorated, the product according to Example 2 of the present invention significantly improved them.
以上説明したような本発明によるときは生産性を害する
ことなしに、強度、成品歩留、耐還元粉化性などを有効
に向上することができ、又焼結鉱中の脈石量を低減する
と共に高温性状を改善し、高炉スラグ比の低減、高炉燃
料比の低減を図ると共に銑鉄中Siの縮減を得しめる有
利な焼結鉱を的確に製造し得るものであるから工業的に
その効果の大きい発明である。According to the present invention as explained above, strength, product yield, resistance to reduction powdering, etc. can be effectively improved without impairing productivity, and the amount of gangue in sintered ore can be reduced. At the same time, it is possible to accurately produce an advantageous sintered ore that improves high-temperature properties, reduces the blast furnace slag ratio, reduces the blast furnace fuel ratio, and reduces the Si content in pig iron, so it is industrially effective. This is a great invention.
【図面の簡単な説明】
図面は本発明の技術的内容を示すもので、第1図は着粉
率と粒度分布の関係を示した図表、第2図はCaOS
i02 FeO系における1150℃以下の低融点領
域を示した説明図である。[Brief explanation of the drawings] The drawings show the technical contents of the present invention. Figure 1 is a chart showing the relationship between powder adhesion rate and particle size distribution, and Figure 2 is a diagram showing the relationship between powder adhesion rate and particle size distribution.
FIG. 2 is an explanatory diagram showing a low melting point region of 1150° C. or lower in the i02 FeO system.
Claims (1)
又は全部を粉砕して粒度調整し、1朋未満の微粉部分の
FeO/5i02を0.8〜2.3となるように調整す
ることを特徴とし、このようVC調整された配合原料を
焼結する焼結鉱の製造方法。 21朋未滴の微粉部分のFeO/5i02を0.8〜2
.3となるように調整すると共に焼結鉱の5i02含有
量が4.6〜5.4となるようVC配合原料のSiO□
含有量を調整する特許請求の範囲第1項に記載の焼結鉱
の製造方法。[Claims] I Part or all of the ore or miscellaneous raw materials containing 6% or more of FeO is pulverized and the particle size is adjusted so that the FeO/5i02 of the fine powder portion of less than 1 tom is 0.8 to 2.3. A method for producing sintered ore by sintering blended raw materials adjusted in this way. 21 FeO/5i02 of the fine powder part of Tomomi drop is 0.8 to 2
.. SiO□ of the VC compounding raw material was adjusted so that the 5i02 content of the sintered ore was 4.6 to 5.4.
The method for producing sintered ore according to claim 1, wherein the content is adjusted.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP13833181A JPS5935969B2 (en) | 1981-09-04 | 1981-09-04 | Method for manufacturing sintered ore |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP13833181A JPS5935969B2 (en) | 1981-09-04 | 1981-09-04 | Method for manufacturing sintered ore |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5839745A JPS5839745A (en) | 1983-03-08 |
| JPS5935969B2 true JPS5935969B2 (en) | 1984-08-31 |
Family
ID=15219400
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP13833181A Expired JPS5935969B2 (en) | 1981-09-04 | 1981-09-04 | Method for manufacturing sintered ore |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5935969B2 (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4661077B2 (en) * | 2004-04-20 | 2011-03-30 | Jfeスチール株式会社 | Method for producing sintered ore |
| CN116855731B (en) * | 2023-06-29 | 2024-12-17 | 鞍钢股份有限公司 | Adjustment method for stabilizing ferrous oxide content of sintering ore |
-
1981
- 1981-09-04 JP JP13833181A patent/JPS5935969B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5839745A (en) | 1983-03-08 |
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