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JPS5943533B2 - Method for producing sintered ore - Google Patents
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JPS5943533B2 - Method for producing sintered ore - Google Patents

Method for producing sintered ore

Info

Publication number
JPS5943533B2
JPS5943533B2 JP1777082A JP1777082A JPS5943533B2 JP S5943533 B2 JPS5943533 B2 JP S5943533B2 JP 1777082 A JP1777082 A JP 1777082A JP 1777082 A JP1777082 A JP 1777082A JP S5943533 B2 JPS5943533 B2 JP S5943533B2
Authority
JP
Japan
Prior art keywords
sintering
sintered
zone
raw material
moisture
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
JP1777082A
Other languages
Japanese (ja)
Other versions
JPS58136727A (en
Inventor
一博 山本
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
Sumitomo Metal Industries Ltd
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 Sumitomo Metal Industries Ltd filed Critical Sumitomo Metal Industries Ltd
Priority to JP1777082A priority Critical patent/JPS5943533B2/en
Publication of JPS58136727A publication Critical patent/JPS58136727A/en
Publication of JPS5943533B2 publication Critical patent/JPS5943533B2/en
Expired legal-status Critical Current

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  • Manufacture And Refinement Of Metals (AREA)

Description

【発明の詳細な説明】 本発明は焼結過程における実焼結時間の短縮を可能なら
しめた焼結鉱の製造方法に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing sintered ore that makes it possible to shorten the actual sintering time in the sintering process.

一般に焼結鉱は各種焼結原料を所要の割合で均質に混合
し、これに水、温水、或いは擬似粒化剤(バインダー)
を加えてドラム、ミキサー等で混練、造粒化し、擬似粒
子を粗大化した後、これを焼結機に装入し、焼結機で点
火して焼結反応を行なわしめ、焼結を完了すると、これ
を破砕し冷却して製造されている。
Generally, sintered ore is made by homogeneously mixing various sintering raw materials in the required ratio, and then adding water, hot water, or a pseudo-granulating agent (binder) to the mixture.
is added, kneaded and granulated using a drum, mixer, etc. to coarsen the pseudo particles, then charged into a sintering machine, ignited in the sintering machine to cause a sintering reaction, and complete sintering. This is then crushed and cooled to produce it.

ところで焼結鉱の生産率は−に実焼結時間の短縮にかか
つていると言っても過言ではなく、実焼結時間の短縮の
ため通気性の改善等様々の方法が試みられており、上述
した如く焼結原料を混練、造粒化し擬似粒子の粗大化を
図るのも通気性改善方法の一つである。
By the way, it is no exaggeration to say that the production rate of sintered ore depends on the shortening of the actual sintering time, and various methods such as improving air permeability have been tried to shorten the actual sintering time. As described above, kneading and granulating the sintering raw material to coarsen the pseudo particles is one method for improving air permeability.

しかし擬似粒子を十分に粗大化するには単一のドラムミ
キサでは不足で、複数のドラムミキサを必要とし、設備
費が高く、その上たとえ粒子の粗大化を図っても焼結過
程で崩壊されることが多く、通気が阻害されて十分な焼
結時間の短縮を図り得なかった。
However, a single drum mixer is not enough to sufficiently coarsen the pseudo-particles; multiple drum mixers are required, equipment costs are high, and even if the particles are coarsened, they will collapse during the sintering process. The sintering time could not be sufficiently shortened due to the large amount of sintering, which impeded ventilation.

焼結過程において擬似粒子が崩壊するのは次のような理
由による。
The reason why the pseudo particles collapse during the sintering process is as follows.

一般に擬似粒子の粗大化が図られた焼結原料は例えばド
ワイト・ロイド焼結機にあってはそのパレット上に順次
所要高さに装入充填された後、その表面に点火され、同
時にパレット移動域下に配した風箱がら空気を吸引する
ことにより、空気をパレット上の焼結充填層表面から下
方に吹抜けさせ、焼結充填層をその表面から順次下方に
焼結せしめてゆくが、この焼結過程において、焼結充填
層内にはその表面側から下方に向けて第8図に示す如く
、焼結帯A、乾燥帯B、水分凝縮帯C及び初期焼結原料
帯りが形成される。
In general, sintered raw materials with coarse pseudo-particles, for example, in a Dwight Lloyd sintering machine, are sequentially charged and filled to the required height on the pallet, then ignited on the surface, and simultaneously moved to the pallet. By suctioning air through a wind box placed below the area, the air is blown downward from the surface of the sintered packed layer on the pallet, and the sintered packed layer is sintered sequentially downward from the surface. In the sintering process, a sintering zone A, a drying zone B, a moisture condensation zone C, and an initial sintering raw material zone are formed in the sintered packed bed from the surface side downwards, as shown in FIG. Ru.

焼結帯Aは既に焼結を完了した領域であり、また乾燥帯
Bは焼結帯Aを経て下方に通流せしめられる高温排ガス
により加熱されて脱水されつつある領域であり、更に水
分凝縮帯Cは乾燥帯Bにて水分を含んだ排ガスが冷却さ
れ、水分が凝縮する領域であり、そして初期焼結原料帯
りは未だ装入充填されたままの焼結原料領域である。
The sintering zone A is an area where sintering has already been completed, and the drying zone B is an area that is being heated and dehydrated by the high-temperature exhaust gas flowing downward through the sintering zone A, and is further a moisture condensation zone. C is a region where the exhaust gas containing moisture is cooled in the drying zone B and the moisture is condensed, and the initial sintering raw material zone is a sintering raw material zone where the initial sintering raw material zone is still charged and filled.

第8図は焼結充填層表面に点火した後、45秒経過した
時点における焼結充填層断面の水分分布を示すグラフで
あって、横軸に水分を、縦軸に焼結原料高さをとって示
してあり、グラフ中りは焼結充填層表面を示している。
FIG. 8 is a graph showing the moisture distribution in the cross section of the sintered packed bed 45 seconds after ignition on the surface of the sintered packed bed, with the horizontal axis representing moisture and the vertical axis representing the height of the sintered raw material. The center of the graph shows the surface of the sintered packed layer.

このグラフから明らかな如く、初期水分が5.8%であ
った焼結原料は焼結帯Aにおいては水分が零に、また乾
燥帯Bでは下部から上方に向うに従って水分が急速に低
減され、更に初期焼結原料帯りでは水分が変化しないに
もかかわらず、水分凝縮帯Cにおいては水分が初期水分
よりも2%前後増加していることが解る。
As is clear from this graph, the moisture content of the sintered raw material, which had an initial moisture content of 5.8%, decreased to zero in the sintering zone A, and in the dry zone B, the moisture content rapidly decreased from the bottom upwards. Furthermore, although the moisture content does not change in the initial sintering raw material zone, it can be seen that the moisture content in the moisture condensation zone C increases by about 2% from the initial moisture content.

この水分凝縮帯Cでの水分の増加が擬似粒子を過剰水分
状態に至らしめ、崩壊、流動化し擬似粒子間の間隙を閉
塞し、通気性を阻害する結果となるのである。
This increase in moisture in the moisture condensation zone C brings the pseudo particles into an excessive moisture state, causing them to collapse and become fluidized, closing the gaps between the pseudo particles and impeding air permeability.

ちなみに各領域での通気抵抗係数(103m−1)の一
例を示すと下記の通りであり、水分凝縮帯Cにおける抵
抗が著しく大きくなっていることが解る。
Incidentally, an example of the ventilation resistance coefficient (103 m-1) in each region is shown below, and it can be seen that the resistance in the water condensation zone C is significantly large.

焼結帯A :23.20乾燥帯B :57.77
水分凝縮帯C: 78.28初期焼結原料帯D:23.
20この対策として焼結原料の混線工程において水、温
水量を減少する方法、或いは粗粒化した焼結原料を焼結
機のパレット上に装入した後、点火を行うに先立って3
00°C前後の排ガスを10〜30秒間通流して予熱乾
燥した後、点火、焼結を行う方法(特開昭55−738
34号)等が提案されている。
Sintering zone A: 23.20 Drying zone B: 57.77
Moisture condensation zone C: 78.28 Initial sintering raw material zone D: 23.
20 As a countermeasure for this, there is a method of reducing the amount of water or hot water in the mixing process of sintering raw materials, or a method of reducing the amount of water or hot water in the mixing process of sintering raw materials, or 3)
A method of preheating and drying by passing exhaust gas around 00°C for 10 to 30 seconds, followed by ignition and sintering (Japanese Patent Application Laid-Open No. 55-738
No. 34) etc. have been proposed.

しかし前者にあっては十分な粗粒化を行うことが出来ず
、また粗粒の強度が低く直ぐ崩壊するなどの欠点があり
、また後者にあっては予熱乾燥によりたしかに焼結過程
での擬似粒子の崩壊が少なく、それだけ通気性が改善さ
れ、実焼結時間が短縮される効果は認められる反面、こ
の予熱乾燥を焼結機のパレット上において行うこととし
ているため、焼結のためのパレット有効面積が減少し、
結果的に生産率は殆んど変らないのが現状である。
However, in the former method, it is not possible to make the grains coarse enough, and the strength of the coarse grains is low and they collapse easily. Although the effect of reducing particle collapse, improving air permeability, and shortening the actual sintering time is recognized, on the other hand, this preheating and drying is performed on the pallet of the sintering machine, so the pallet for sintering is The effective area is reduced,
As a result, the current situation is that the production rate remains almost unchanged.

本発明はかかる事情に鑑みなされたものであって、その
目的とするところは焼結原料を混練して擬似粒子を粗大
化し、これを乾燥水分除去率が40係以下となるよう乾
燥した後、焼結機に装入することによって、焼結鉱生産
率及び品質の大幅な向上を図れ、また焼結過程でのNO
x発生量の低減も達成し得るようにした焼結鉱の製造方
法を提供するにある。
The present invention was created in view of the above circumstances, and its purpose is to knead sintering raw materials to coarsen pseudo particles, dry them so that the dry moisture removal rate is 40 coefficients or less, and then By charging the sinter into the sintering machine, the production rate and quality of sintered ore can be greatly improved, and NO
It is an object of the present invention to provide a method for producing sintered ore that can also reduce the amount of x generated.

以下本発明を図面に基き具体的に説面する第1図は本発
明方法に係る焼結鉱の製造方法(以下本発明方法という
)を工程順に示すブロック図、第2図は焼結原料の乾燥
及び装入工程を示す模式図であり、図中1は焼結原料の
計量・切出工程、2は焼結原料の混合工程、3は水、温
水、或いは擬似粒化剤を添加してその混線、擬似粒子の
粗粒化を行う造粒工程、4は乾燥工程、5は焼結機への
装入工程、6は焼結工程を示している。
Hereinafter, the present invention will be explained in detail based on the drawings. Figure 1 is a block diagram showing the process order of the method for producing sintered ore according to the method of the present invention (hereinafter referred to as the method of the present invention), and Figure 2 is a block diagram of the sintered raw material. This is a schematic diagram showing the drying and charging process, in which 1 is the measuring and cutting process of the sintering raw material, 2 is the mixing process of the sintering raw material, and 3 is the process of adding water, hot water, or a pseudo-granulating agent. A granulation process for coarsening the pseudo particles, 4 a drying process, 5 a charging process to a sintering machine, and 6 a sintering process.

先ず各種焼結原料は夫々予め設定された配合比に合せて
計量され、切出され(計量・切出工程1)、バッグミル
等にて均質に混合しく混合工程2)、混合した焼結原料
をドラムミキサにて水、温水、或いは擬似粒化剤のもと
で混練し、造粒化して擬似粒子を粗大化する(造粒工程
3)。
First, various sintering raw materials are weighed and cut out according to preset mixing ratios (weighing/cutting process 1), mixed homogeneously in a bag mill, etc. (mixing process 2), and the mixed sintering raw materials are The mixture is kneaded in water, hot water, or a pseudo-granulating agent in a drum mixer, and granulated to coarsen the pseudo-particles (granulation step 3).

擬似粒子に対する擬似粒子の粗大化の程度は粒子として
の十分な強度を維持出来、しかも十分な通風機能が得ら
れるよう適宜に設定する。
The degree of coarsening of the pseudo particles relative to the pseudo particles is appropriately set so that sufficient strength as particles can be maintained and sufficient ventilation function can be obtained.

擬似粒子の粗大化を行った焼結原料は第2図に示す如く
サージホッパ41に導入し、サージホッパ41から焼結
機42のパレット42a上に供給されてゆくこととなる
が、これに先立ってサージホッパ41内にて焼結原料の
乾燥を行う(乾燥工程4)。
The sintering raw material that has undergone coarsening of pseudo particles is introduced into the surge hopper 41 as shown in FIG. 2, and is supplied from the surge hopper 41 onto the pallet 42a of the sintering machine 42. The sintering raw material is dried in 41 (drying step 4).

サージホッパ41は焼結機42における一端、即ち給鉱
端の上方であって、床敷ホッパ43の直ぐ下流側に位置
させて併設されており、その給送口にはロールフィーダ
41a及びこれから切り出された焼結原料をパレツ)4
2a上に導くディフレクタプレート41bが配設されて
いる。
The surge hopper 41 is located above one end of the sintering machine 42, that is, the ore feed end, and is located immediately downstream of the bedding hopper 43, and has a roll feeder 41a and the ore cut from the roll feeder 41a at its feed opening. Pallets of sintered raw materials) 4
A deflector plate 41b is provided that guides the deflector onto 2a.

床敷ホッパ43には床敷鉱が、またサージホッパ41内
には前述した焼結原料が供給されており、床敷ホッパ4
3から床敷鉱が供給され、この上に所要高さにわたって
サージホッパ41から焼結原料が供給されることとなる
The bedding hopper 43 is supplied with bedding ore, and the surge hopper 41 is supplied with the above-mentioned sintering raw material.
The bedding ore is supplied from 3, and the sintering raw material is supplied from the surge hopper 41 over the bedding ore over the required height.

ところでこのサージホッパ41内には送出口の上方に全
体がジヨウ口の頭部状をなし、上面に多数の噴射孔41
Cを開口させた熱風の吹出ノズル41dが配設されてい
る。
By the way, the inside of this surge hopper 41 has a head-like shape as a whole above the outlet, and a large number of injection holes 41 are provided on the upper surface.
A hot air blowing nozzle 41d with an opening C is provided.

吹出ノズル41dにはサージホッパ41の周壁を貫通せ
しめた熱風供給管41eの一端が連結され、その他端は
途中にブロワ41fを介在せしめて焼結機42の風箱4
5に連らなる排風ダクト45aに連結されている。
One end of a hot air supply pipe 41e penetrating the peripheral wall of the surge hopper 41 is connected to the blowout nozzle 41d, and the other end is connected to the air box 4 of the sintering machine 42 with a blower 41f interposed in the middle.
The exhaust duct 45a is connected to the exhaust duct 45a.

排風ダク)45aには各風箱45を通じて吸引回収した
焼結排ガス(80〜120℃程度)が通流しており、こ
れがブロワ41f、熱風供給管41eを通じて吹出ノズ
ル41dの噴射孔41cからサージホッパ41内に上方
に向は噴き出されるようになっている。
The sintered exhaust gas (approximately 80 to 120°C) sucked and collected through each wind box 45 flows through the exhaust duct) 45a, and this flows through the blower 41f and the hot air supply pipe 41e to the surge hopper 41 from the injection hole 41c of the blowout nozzle 41d. It is designed to be ejected inwardly and upwardly.

サージホッパ41内に吹き出された排ガスは焼結原料の
擬似粒子間に形成されている隙間を通じて上方に通流さ
れる。
The exhaust gas blown into the surge hopper 41 flows upward through the gaps formed between the pseudo particles of the sintering raw material.

これによって焼結原料は下式で定義される乾燥水分除去
率−が40%以下になる迄乾燥される。
As a result, the sintered raw material is dried until the dry moisture removal rate - defined by the following formula becomes 40% or less.

乾燥水分除去率(イ)を40係以下とするのは40係を
超えると擬似粒子強度が急激に低下(第4図参照)して
焼結過程での水分凝縮帯で擬似粒子の崩壊を生じ易く、
また焼結鉱生産率の増減率も低下しく第5図参照)、還
元粉化率が増大しく第6図参照)、更に焼結過程でのN
Ox発生量が急増(第7図参照)することになる。
The reason why the dry moisture removal rate (a) is set to 40 factors or less is because if it exceeds 40 factors, the strength of the pseudo particles will decrease rapidly (see Figure 4) and the pseudo particles will collapse in the moisture condensation zone during the sintering process. Easy,
In addition, the rate of change in the sinter production rate decreases (see Figure 5), the reduction powdering rate increases (see Figure 6), and the N
The amount of Ox generated will increase rapidly (see Figure 7).

なお上記擬似粒子強度(イ)は5〜2mmの擬似粒子2
00gと、これを1mの高さから厚さ10mmの鉄板上
に10回落下させた後における5〜2mmの擬似粒子重
量(g)との百分率により与える。
The above pseudo particle strength (a) is 5 to 2 mm pseudo particle 2.
00g and the weight (g) of pseudo particles of 5 to 2 mm after dropping this 10 times from a height of 1 m onto a 10 mm thick iron plate (g).

焼結機42のパレッ)42aは駆動スプロケット42d
と図示しない遊動スプロケットとの間を白抜矢符方向に
周回回動せしめられるよう構成されており、このパレツ
)42aの移動域上方には前記サージホッパ41の下流
側に位置して点火炉44が、また下方には前記点火炉4
4と対向する位置から図示しない排出端近傍にわたって
風箱45が連設配置され、図示しないフ七ワにて風を吸
引し、焼結充填層表面から、下方に風を吹き抜けさせ、
点火炉にて焼結庫料をその表面から順次下方に焼結せし
めてゆくようにしである。
The pallet 42a of the sintering machine 42 is a driving sprocket 42d.
An ignition furnace 44 is located above the movement area of the pallet 42a on the downstream side of the surge hopper 41. , and below is the ignition furnace 4.
A wind box 45 is arranged in series from a position facing 4 to near the discharge end (not shown), sucks the wind with a flap (not shown), and blows the wind downward from the surface of the sintered packed bed.
The sintered material is sequentially sintered from the surface downward in an ignition furnace.

第3図は造粒後の原料水分5.7係のものを乾燥水分除
去率25%とした原料の焼結充填層表面に点火後、60
秒経過した時点での焼結充填層断面における水分(イ)
の測定結果を示すグラフであって、横軸に水分(イ)を
、縦軸に焼結充填層の高さくmm)をとって示しており
、グラフ中人は焼結帯、Bは乾燥帯、Cは水分凝縮帯、
Dは初期焼結原料帯を示している。
Figure 3 shows the surface of the sintered packed bed of the raw material with a dry moisture removal rate of 25% for the raw material moisture content after granulation of 5.7% after ignition.
Moisture in the cross section of the sintered packed bed after seconds have elapsed (a)
This is a graph showing the measurement results of , where the horizontal axis shows moisture (A) and the vertical axis shows the height of the sintered packed layer (mm), where the middle part of the graph is the sintered zone and B is the dry zone. , C is the water condensation zone,
D indicates an initial sintering raw material zone.

このグラフと第8図に示す従来方法による場合のグラフ
とを比較すれば明らかな如く、水分凝縮帯Cにおける水
分が従来方法によった場合には8係近くになるのに対し
、本発明方法に依った場合には4.5係程度であり、水
分凝縮帯Cでの水分が著しく低減せしめられており、そ
れだけ水分凝縮帯Cにおいての擬似粒子の崩壊、流動化
が抑制されるであろうことが容易に推測し得る。
As is clear from a comparison between this graph and the graph for the conventional method shown in FIG. The coefficient is about 4.5, which means that the moisture in the moisture condensation zone C is significantly reduced, and the disintegration and fluidization of pseudo particles in the moisture condensation zone C will be suppressed to that extent. This can be easily inferred.

次に本発明方法に依る場合の各種試験結果について説明
する。
Next, various test results using the method of the present invention will be explained.

試験においては表1に示す如き3種類の配合割合をもつ
供試材t、n、mを用い、これに粉コークスを3.75
%添加し、混練に際しては供試材■には水5,0%、供
試材Hには水5.5係、供試材■には水6.0%を加え
、夫々コンクリートミキサ(内径600mm、長さ60
0mm)に入れて24r、p、mで駆動し、4分間混練
粒造化を行い夫々表2に示す如き粒度分布を有する供試
材■(粗粒原料)、供試材■(通常原料)、供試材■(
細粒原料)を得た。
In the test, test materials t, n, and m having three types of blending ratios as shown in Table 1 were used, and coke powder was added at 3.75%.
%, and when kneading, add 5.0% water to sample material ■, 5.5% water to sample material H, and 6.0% water to sample material ■, using a concrete mixer (inner diameter 600mm, length 60
0 mm) and was driven at 24r, p, m, kneaded and granulated for 4 minutes, and had particle size distributions as shown in Table 2, respectively. Test material■(
A fine grain raw material) was obtained.

次にこれを略105°Cに維持した乾燥機にて種々の乾
燥水分除去率(イ)を設定し、これを焼結試験鍋(頂部
内径300mm、底部内径280mm、高さ4007n
りにて点火焼結した。
Next, various drying moisture removal rates (a) were set in a dryer maintained at approximately 105°C, and this was dried in a sintering test pot (top inner diameter 300 mm, bottom inner diameter 280 mm, height 4007 nm).
The material was ignited and sintered.

結果は第4〜7図に示す通りである。The results are shown in Figures 4-7.

第4図は擬似粒子強度と乾燥水分除去率との関係を示す
グラフであって、横軸に乾燥水分除去率(イ)を、縦軸
に擬似粒子強度(イ)をとって示してあり、グラフ中■
は供試材■、■は供試材■、■は供試材■の結果を示し
ている。
FIG. 4 is a graph showing the relationship between pseudo particle strength and dry moisture removal rate, with the dry moisture removal rate (A) on the horizontal axis and the pseudo particle strength (A) on the vertical axis. In the graph■
indicates the results for the sample material ■, ■ indicates the results for the sample material ■, and ■ indicates the results for the sample material ■.

このグラフから明らかな如く、供試材1.II、Hのい
ずれの場合も、乾燥工程における乾燥水分除去率(イ)
が40%を越えると擬似粒子強度が急速に低下するが、
本発明方法にあっては乾燥水分除去率(イ)を40%以
下に設定されているため、擬似粒子強度が大きく、焼結
過程での粒子の崩壊を防止し得ることが推測し得る。
As is clear from this graph, sample material 1. In both cases II and H, the drying moisture removal rate in the drying process (a)
When exceeds 40%, the pseudo particle strength decreases rapidly, but
In the method of the present invention, since the dry moisture removal rate (a) is set to 40% or less, it can be inferred that the strength of the pseudo particles is high and that it is possible to prevent the particles from collapsing during the sintering process.

第5図は焼結鉱の生産率と乾燥水分除去率との関係を示
すグラフであって、横軸に乾燥水分除去率(イ)を、縦
軸に生産率の増減率(乾燥水分除去率0チのときの生産
率を100とする)をとって示してあり、グラフ中1.
n、IIIは夫々供試材I。
Figure 5 is a graph showing the relationship between the production rate of sintered ore and the dry moisture removal rate. The production rate at 0 is 100).
n and III are sample materials I, respectively.

■、■の結果を示している。The results of ■ and ■ are shown.

このグラフから明らかな如く、供試材1.n、IIIの
いずれも乾燥水分除去率が20%近傍で生産率が最も高
くなり、供試材■では40係、供試材1では60%を越
えると急激に低下するが、本発明方法にあっては乾燥水
分除去率を40係以下に設定しであるため、生産率の大
幅な向上が可能となっている。
As is clear from this graph, sample material 1. For both No. Since the drying moisture removal rate is set to 40% or less, it is possible to significantly improve the production rate.

また供試材1.n、III相互の比較では粗粒化の程度
が大きい程生産率も高くなっている。
Also, sample material 1. In comparison between No. n and III, the larger the degree of coarse graining, the higher the production rate.

第6図は焼結鉱品質の指標として重視される還元粉化率
と乾燥水分除去率との関係を示すグラフであって、横軸
に乾燥水分除去率を、縦軸に還元粉化率をとって示して
おり、グラフ中1.II、IIIは夫々供試材1.n、
Hの結果を示している。
Figure 6 is a graph showing the relationship between the reduction pulverization rate and the dry moisture removal rate, which are important indicators of sintered ore quality, with the dry moisture removal rate on the horizontal axis and the reduction pulverization rate on the vertical axis. 1 in the graph. II and III are sample materials 1. n,
The results of H are shown.

このグラフから明らかな如く、供試材1.IIにあって
は乾燥水分除去率が80係を、また供試材■にあっては
60%を越えると急速に低下するが、本発明方法にあっ
ては乾燥水分除去率を40係以下に設定することとして
いるから、還元粉化率の大幅な向上も図れることが解る
As is clear from this graph, sample material 1. When the dry moisture removal rate exceeds 80% for II and 60% for test material II, it rapidly decreases, but in the method of the present invention, the dry moisture removal rate can be reduced to 40% or less. It can be seen that the reduction and powdering rate can be significantly improved by setting the following conditions.

また供試材1 、 II。■相互の比較においては原料
粒度が中程度である供試材■において乾燥水分除去率(
イ)の効果が最も大きいことが解る。
Also, sample materials 1 and II. ■In mutual comparison, the dry moisture removal rate (
It can be seen that b) has the largest effect.

第7図は焼結過程で生ずるNOx発生量と乾燥水分除去
率との関係を示すグラフであり、横軸に乾燥水分除去率
(イ)を、才た縦軸にNOx発生量の増減率(乾燥水分
除去率o%のときの増減率を1oo%とする)をとって
示してあり、グラフ中1、n、111は夫々供試材1.
II、IIIについての結果を示している。
FIG. 7 is a graph showing the relationship between the amount of NOx generated during the sintering process and the dry moisture removal rate. In the graph, 1, n, and 111 indicate sample material 1.1, n, and 111, respectively.
The results for II and III are shown.

このグラフから明らかな如く、供給材1.II、III
のいずれもが、乾燥水分除去率20係前後において最低
値を示しており、また70〜90係を越えると従来より
もNOx発生量が大きくなるが、本発明方法にあっては
乾燥水分除去率を40係以下に設定しているため、NO
x発生量の大幅な低減が可能となっている。
As is clear from this graph, supply material 1. II, III
Both show the lowest values when the dry moisture removal rate is around 20 units, and when the dry moisture removal rate exceeds 70 to 90 units, the amount of NOx generated becomes larger than conventional methods, but in the method of the present invention, the dry moisture removal rate Since it is set to 40 sections or less, NO
This makes it possible to significantly reduce the amount of x generated.

供試材1、n、III相互の比較においては原料粒度が
小さい程NOx発生量が少なくなっている。
In comparing sample materials 1, n, and III, the smaller the raw material particle size, the smaller the amount of NOx generated.

なお上述の実施例においては造粒化した後の焼結原料を
焼結機に供給するためのサージホッパ41を利用して乾
燥を行う構成を示したが、何らこれに限るものではなく
、例えば別に乾燥機を設置し、焼結原料をこの乾燥機に
よって所要の乾燥水分率(イ)となるよう乾燥した後、
サージホッパ41に導入することとしてもよい。
In addition, in the above-mentioned embodiment, a configuration was shown in which drying is performed using the surge hopper 41 for supplying the sintering raw material after granulation to the sintering machine, but the invention is not limited to this in any way. After installing a dryer and drying the sintering raw material to the required dry moisture content (a),
It may also be introduced into the surge hopper 41.

また乾燥のための熱源として実施例では焼結排ガスを利
用する構成につき説明したが、各種の炉の排ガスを利用
してよいことは言うまでもない。
Furthermore, although the embodiments have described a configuration in which sintering exhaust gas is used as a heat source for drying, it goes without saying that exhaust gas from various types of furnaces may be used.

以上の如く本発明方法にあっては焼結原料を混練して粒
状化し、これを乾燥水分除去率が40係以下となるよう
乾燥した後、焼結機に装入することとしているから、焼
結機における焼結のための有効面積が伺ら縮小されるこ
とがなく、また焼結過程の水分凝縮帯においても、水分
の増加が著しく抑制されて擬似粒子の崩壊が防止され、
焼結過程での通風が阻害されることがなく、大幅な実焼
結時間の短縮により焼結生産性の向上が図れ、また還元
粉化率の向上、NOx発生量の制御を図り得るなど、本
発明は優れた効果を奏するものである。
As described above, in the method of the present invention, the sintering raw materials are kneaded and granulated, dried so that the dry moisture removal rate is 40 coefficients or less, and then charged into the sintering machine. The effective area for sintering in the sintering machine is not reduced in any way, and even in the moisture condensation zone during the sintering process, the increase in moisture is significantly suppressed and the collapse of pseudo particles is prevented.
Ventilation during the sintering process is not obstructed, and sintering productivity can be improved by significantly shortening the actual sintering time. Also, it is possible to improve the reduction powdering rate and control the amount of NOx generated. The present invention has excellent effects.

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

第1図は本発明方法を工程順に示すブロック図、第2図
は同じく乾燥工程及び装入工程を示す模式図、第3図は
同じく焼結過程における焼結充填層の水分分布を示すグ
ラフ、第4〜7図は本発明方法による焼結鉱及び中間品
についての試験結果を示すグラフ、第8図は従来方法に
おける焼結過程での水分分布を示すグラフである。 1・・・・・・計量、切出工程、2・・・・・・混合工
程、3・・・・・・造粒工程、4・・・・・・乾燥工程
、5・・・・・・装入工程、6・・・・・・点火焼結工
程、41・・・・・・サージホッパ、41a・・・・・
・ロールフィーダ、41b・・・・・・ディフレクタプ
レート、41c・・・・・・噴射孔、41d・・・・・
・吹出ノズル、41e・・・・・・供給管、41f・・
・・・・ブロワ、42・・・・・・焼結機、43・・・
・・・床敷ホッパ、44・・・・・・点火炉、45・・
・・・・風箱、45a・・・・・・排気ダクト。
FIG. 1 is a block diagram showing the method of the present invention in the order of steps, FIG. 2 is a schematic diagram showing the drying process and charging process, and FIG. 3 is a graph showing the moisture distribution of the sintered packed bed during the sintering process. 4 to 7 are graphs showing the test results for sintered ore and intermediate products according to the method of the present invention, and FIG. 8 is a graph showing the moisture distribution during the sintering process according to the conventional method. 1...Measuring, cutting process, 2...Mixing process, 3...Pelletization process, 4...Drying process, 5...・Charging process, 6...Ignition sintering process, 41...Surge hopper, 41a...
・Roll feeder, 41b... Deflector plate, 41c... Injection hole, 41d...
・Blowout nozzle, 41e... Supply pipe, 41f...
...Blower, 42...Sintering machine, 43...
...Bedding hopper, 44...Ignition furnace, 45...
...Wind box, 45a...Exhaust duct.

Claims (1)

【特許請求の範囲】 1 焼結原料を混練して擬似粒子を粗大化し、これを下
式に示す乾燥水分除去率が40%以下となるよう乾燥し
た後、焼結機に装入することを特徴とする焼結鉱の製造
方法。 乾燥水分除去率(イ)
[Claims] 1. Knead the sintering raw materials to coarsen the pseudo particles, dry them so that the dry moisture removal rate shown by the formula below is 40% or less, and then charge them into the sintering machine. Characteristic method for producing sintered ore. Dry moisture removal rate (a)
JP1777082A 1982-02-05 1982-02-05 Method for producing sintered ore Expired JPS5943533B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1777082A JPS5943533B2 (en) 1982-02-05 1982-02-05 Method for producing sintered ore

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1777082A JPS5943533B2 (en) 1982-02-05 1982-02-05 Method for producing sintered ore

Publications (2)

Publication Number Publication Date
JPS58136727A JPS58136727A (en) 1983-08-13
JPS5943533B2 true JPS5943533B2 (en) 1984-10-23

Family

ID=11952945

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1777082A Expired JPS5943533B2 (en) 1982-02-05 1982-02-05 Method for producing sintered ore

Country Status (1)

Country Link
JP (1) JPS5943533B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5020501B2 (en) * 2005-11-17 2012-09-05 新日本製鐵株式会社 Pretreatment method of sintered raw material and method of manufacturing sintered ore

Also Published As

Publication number Publication date
JPS58136727A (en) 1983-08-13

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