JPS63130730A - Production of reduced chromium ore pellet - Google Patents
Production of reduced chromium ore pelletInfo
- Publication number
- JPS63130730A JPS63130730A JP27804886A JP27804886A JPS63130730A JP S63130730 A JPS63130730 A JP S63130730A JP 27804886 A JP27804886 A JP 27804886A JP 27804886 A JP27804886 A JP 27804886A JP S63130730 A JPS63130730 A JP S63130730A
- Authority
- JP
- Japan
- Prior art keywords
- pellets
- chamber
- rotary kiln
- preheater
- chromium 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.)
- Granted
Links
- 239000008188 pellet Substances 0.000 title claims abstract description 48
- 229910052804 chromium Inorganic materials 0.000 title claims abstract description 23
- 239000011651 chromium Substances 0.000 title claims abstract description 23
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 title claims abstract description 21
- 238000004519 manufacturing process Methods 0.000 title claims description 10
- 229910001868 water Inorganic materials 0.000 claims abstract description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 12
- 238000002485 combustion reaction Methods 0.000 claims description 14
- 238000001816 cooling Methods 0.000 claims description 3
- 239000007789 gas Substances 0.000 abstract description 40
- 239000003575 carbonaceous material Substances 0.000 abstract description 15
- 238000005261 decarburization Methods 0.000 abstract description 11
- 239000007921 spray Substances 0.000 abstract description 8
- 239000002344 surface layer Substances 0.000 abstract description 8
- 238000006243 chemical reaction Methods 0.000 abstract description 7
- 239000000203 mixture Substances 0.000 abstract description 3
- 239000003638 chemical reducing agent Substances 0.000 abstract description 2
- 230000001590 oxidative effect Effects 0.000 abstract description 2
- 239000000567 combustion gas Substances 0.000 abstract 2
- 239000002699 waste material Substances 0.000 abstract 2
- 239000011230 binding agent Substances 0.000 abstract 1
- 238000005453 pelletization Methods 0.000 abstract 1
- 238000005507 spraying Methods 0.000 abstract 1
- 238000000034 method Methods 0.000 description 11
- 229910052799 carbon Inorganic materials 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000000571 coke Substances 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 229910052742 iron Inorganic materials 0.000 description 3
- 239000003595 mist Substances 0.000 description 3
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 2
- 238000007664 blowing Methods 0.000 description 2
- 239000003546 flue gas Substances 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- 239000000440 bentonite Substances 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
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 239000002737 fuel gas Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
Landscapes
- Manufacture And Refinement Of Metals (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は還元クロム鉱石ペレットを予熱機とロータリー
キルンとを連設した還元炉(グレートキルン)によって
製造する工程において、ロータリーキルンから予熱機に
入るキルンの燃焼排ガスの温度を下げることによって、
予熱機内でのペレット表層部の内装炭材と排ガス中co
2、H2Oとの脱炭反応を抑制し、還元に寄与する炭材
歩留を向上させ、もって還元クロム鉱石ペレットの還元
率を向上させる技術に関する。[Detailed Description of the Invention] [Field of Industrial Application] The present invention relates to a process for producing reduced chromium ore pellets in a reduction furnace (great kiln) that is connected to a preheater and a rotary kiln. By lowering the temperature of the combustion exhaust gas,
Internal carbon material on the pellet surface layer and CO in the exhaust gas in the preheating machine
2. This invention relates to a technique for suppressing the decarburization reaction with H2O, improving the yield of carbonaceous material contributing to reduction, and thereby improving the reduction rate of reduced chromium ore pellets.
グレートキルンを用いた還元クロム鉱石ペレットの製造
プロセスにおいて、従来、ロータリーキルンの燃焼排ガ
ス温度を低下させるように制御する手段は存在しなかっ
た。それどころか鉄鉱石ペレットを製造するプロセスに
おいては、むしろ逆に燃焼排ガスをさらに加熱するため
のバーナが設置されているほどである。In the production process of reduced chromium ore pellets using a grate kiln, there has conventionally been no means for controlling the temperature of the combustion exhaust gas of the rotary kiln to be lowered. In fact, in the process of manufacturing iron ore pellets, burners are even installed to further heat the combustion exhaust gas.
従来のプロセスでは、予熱機内でのガスと接触するペレ
ット表層部の内装炭材とロータリーキルンからの燃焼排
ガス中CO2,H20との脱炭反応
C+CO2→2CO
C+H20→CO+H2
が不可避であり、脱炭量は全内装炭材量の約20%にも
達していた。その結果、グレートキルンによる還元クロ
ム鉱石ペレットの還元率は最大でも約80%が限界であ
った。In the conventional process, the decarburization reaction C+CO2→2CO C+H20→CO+H2 between the internal carbon material on the surface layer of the pellet that comes into contact with the gas in the preheater and the CO2 and H20 in the combustion exhaust gas from the rotary kiln is unavoidable, and the amount of decarburization is This amounted to approximately 20% of the total amount of interior carbon material. As a result, the maximum reduction rate of reduced chromium ore pellets using a great kiln was limited to about 80%.
本発明は予熱機内での脱炭量を最小限に抑制する方法を
提供するものであり、還元クロム鉱石ペレットの還元率
の飛躍的向上を可能ならしめることを目的とするもので
ある。The present invention provides a method for minimizing the amount of decarburization in a preheater, and aims to dramatically improve the reduction rate of reduced chromium ore pellets.
本発明は、予熱機とロータリーキルンとを連設した還元
炉(グレートキルン)で還元クロム鉱石ペレットを製造
するに際し、ロータリーキルンから予熱機に流入する燃
焼排ガス温度を、ペレットの還元率に応じて制御するこ
とを特徴とする還元クロム鉱石ペレットの製造方法であ
る。The present invention controls the temperature of the combustion exhaust gas flowing from the rotary kiln into the preheater in accordance with the reduction rate of the pellets when producing reduced chromium ore pellets in a reduction furnace (great kiln) in which a preheater and a rotary kiln are connected. This is a method for producing reduced chromium ore pellets.
また本発明の好ましい実施態様としてロータリーキルン
から予熱機に流入する燃焼排ガス温度調節を散水冷却に
より行うことを特徴とする還元クロム鉱石ペレットの製
造方法である。A preferred embodiment of the present invention is a method for producing reduced chromium ore pellets, characterized in that the temperature of the combustion exhaust gas flowing from the rotary kiln into the preheater is controlled by water cooling.
ロータリーキルンと予熱機の連結部近傍あるいは予熱機
内側に所望数のスプレー散水ノズルを配し、ロータリー
キルンから予熱機に流入する燃焼排ガスを直接、散水冷
却することにより、燃焼排ガス温度を下げ、もって既述
の脱炭反応を抑制し、予熱ペレット表層部の内装炭材歩
留を向上させて、還元率の向上を図る。A desired number of spray water nozzles are arranged near the joint between the rotary kiln and the preheater or inside the preheater, and the combustion exhaust gas flowing from the rotary kiln into the preheater is directly sprayed and cooled, thereby lowering the combustion exhaust gas temperature and achieving the above-mentioned results. This aims to improve the reduction rate by suppressing the decarburization reaction and improving the internal carbon material yield in the surface layer of the preheated pellets.
グレートキルンを用いて還元クロム鉱石ペレットを製造
するプロセスフローシートの一例を第1図に示す。An example of a process flow sheet for producing reduced chromium ore pellets using a grate kiln is shown in FIG.
まず、粉状のクロム鉱石と還元材としての微粉コークス
および少量の粘結材、例えばベントナイトを所定の割合
で混合したものをディスクペレタイザlで例えば15〜
20mmに加湿造粒してグリーンペレットとする。クロ
ム鉱石は金属酸化物としてFeおよびCr酸化物(Fe
OlCr203 )を含み、これらを内装炭材(C:8
0〜90重量%のコークス)により、高温(1300−
1400℃)のロータリーキルン4内で次式に従って還
元する。First, a mixture of powdered chromium ore, fine coke as a reducing agent, and a small amount of caking agent such as bentonite in a predetermined ratio is mixed with a disk pelletizer l for example
Humidify and granulate to 20 mm to obtain green pellets. Chromium ore contains Fe and Cr oxide (Fe
OlCr203), and these are used as interior carbon material (C:8
0 to 90 wt. % coke) at high temperatures (1300-
Reduction is carried out in a rotary kiln 4 at a temperature of 1400° C. according to the following formula.
7Cr20B+27C
+2Cr7 C3+21CO
7FeO+I OC−+Fe7 C3+7CO内装炭
材はこれらCr、Fe酸化物を100%還元するに必要
な量を添加するのが一般的であり、造粒されたグリーン
ペレットのカーボン含有量は鉱石の種類によって異なる
が、通常15〜17重量%程度である。7Cr20B+27C +2Cr7 C3+21CO 7FeO+I OC-+Fe7 C3+7CO It is common to add the necessary amount of internal carbon material to reduce these Cr and Fe oxides by 100%, and the carbon content of the granulated green pellets is the same as that of the ore. Although it varies depending on the type, it is usually about 15 to 17% by weight.
造粒されたグリーンペレットは予熱機2でグレートコン
ベア3によって搬送されながら乾燥加熱される。予熱機
2は通常3室に分れており、ガス温度は例えば第3室は
220 ’(!、第2室は550℃、第1室はtooo
℃となっており、特に第1室はロータリーキルン4から
の燃焼排ガスが直接入り込む室であるため、ガス温度が
最も高い。予熱機2で予熱されたペレットは高温のロー
タリーキルン4内に入すバーナ6により加熱還元された
後、クーラ5で冷却されて成品である還元クロム鉱石ペ
レットとなる。ロータリーキルン4の燃焼排ガス組成は
、例えば、
H2O:15.6%
CO:4.1%、
CO2:13.5%
N2:66.8%
のように酸化性ガス(H20+CO2)を約30%含ん
でおり、かつ、ガス温度が約1000℃と高温であるた
め、予熱機2の第1室においてペレット表層部に存在す
る炭材が
C+H20→CO+H2
C+CO2→2CO
の反応によって脱炭される。この量は一般に全内装炭材
の約20%にも達するため、従来のプロセスでは還元ペ
レットの還元率80%の達成が限界であった。The granulated green pellets are dried and heated in a preheater 2 while being conveyed by a great conveyor 3. The preheater 2 is usually divided into three chambers, and the gas temperature is, for example, 220°C in the third chamber (!, 550°C in the second chamber, and too much in the first chamber).
℃, and in particular, the first chamber is the chamber into which the combustion exhaust gas from the rotary kiln 4 directly enters, so the gas temperature is the highest. The pellets preheated by the preheater 2 are heated and reduced by a burner 6 placed in a high-temperature rotary kiln 4, and then cooled by a cooler 5 to become reduced chromium ore pellets. The combustion exhaust gas composition of the rotary kiln 4 contains about 30% of oxidizing gas (H20 + CO2), for example, H2O: 15.6% CO: 4.1%, CO2: 13.5% N2: 66.8%. In addition, since the gas temperature is as high as about 1000° C., the carbon material present in the surface layer of the pellet in the first chamber of the preheater 2 is decarburized by the reaction C+H20→CO+H2 C+CO2→2CO. Since this amount generally reaches about 20% of the total internal carbonaceous material, achieving a reduction rate of 80% of the reduced pellets was the limit in conventional processes.
第1表にCO2:30%、N2ニア0%の雰囲気下に実
機で製造したグリーンペレットを60分間放置した場合
の脱炭量と温度との関係を示す。Table 1 shows the relationship between the amount of decarburization and temperature when green pellets produced using an actual machine were left for 60 minutes in an atmosphere of 30% CO2 and 0% N2.
第1表から温度1000℃から800℃への低下により
、
CO2+C=2CO
の反応でグリーンペレットから除かれる炭材量は約1/
3となり、燃焼排ガス温度の低下が予熱機2の第1室で
の内装炭材の歩留向上に大きな効果のあることが分る。From Table 1, as the temperature decreases from 1000°C to 800°C, the amount of carbon material removed from the green pellets by the reaction of CO2+C=2CO is approximately 1/
3, which shows that the reduction in combustion exhaust gas temperature has a great effect on improving the yield of interior carbon material in the first chamber of the preheater 2.
それ故、ロータリーキルンからの高温の排ガスが直接流
入する予熱機2の第1室内、あるいは予熱機2とロータ
リーキルン4との連結部近傍にスプレーノズル7を配し
、燃焼排ガス8に直接スプレー散水してガス温度を低下
させることにより脱炭反応を抑制し、ペレット表層部の
炭材歩留を飛躍的に向上させることができる。尚、散水
した水滴の蒸発を早め、ガスの冷却効率を高める意味か
ら、スプレーはミストスプレーを用いるのが望ましい。Therefore, the spray nozzle 7 is arranged in the first chamber of the preheater 2 into which the high-temperature exhaust gas from the rotary kiln directly flows, or near the connection between the preheater 2 and the rotary kiln 4, and sprays water directly onto the combustion exhaust gas 8. By lowering the gas temperature, the decarburization reaction can be suppressed and the yield of carbonaceous material in the surface layer of the pellet can be dramatically improved. Note that it is desirable to use a mist spray to speed up the evaporation of the sprinkled water droplets and increase the cooling efficiency of the gas.
上記実験結果をもとに、実機にてスプレー散水によるキ
ルン燃焼排ガス温度制御実験を行い、還元クロム鉱石ペ
レットの還元率に及ぼすキルン燃焼排ガス温度の影響を
調査した。結果を第2図に示す。キルン排ガス温度が7
80℃前後で還元率は最大値を示す。この理由は第3図
(a)に示すように、キルン排ガス温度の低下とともに
予熱機内でのペレットからの脱炭量は減少するが、温度
を下げ過ぎるとキルン内での熱不足に陥り、ペレットの
温度が十分に上がらずに内装炭材が還元に有効に利用さ
れず、第3図(b)に示すように、成品ペレット中にフ
リーカーボンとして残留するカーボンが増加するためで
ある。Based on the above experimental results, an experiment was conducted to control the temperature of kiln flue gas using spray water using an actual machine, and the effect of kiln flue gas temperature on the reduction rate of reduced chromium ore pellets was investigated. The results are shown in Figure 2. Kiln exhaust gas temperature is 7
The reduction rate reaches its maximum value at around 80°C. The reason for this is as shown in Figure 3 (a), as the temperature of the kiln exhaust gas decreases, the amount of decarburization from the pellets in the preheater decreases, but if the temperature is lowered too much, there will be a lack of heat in the kiln, and the pellets will be decarburized. This is because the internal carbon material is not effectively used for reduction because the temperature of the pellet does not rise sufficiently, and as shown in FIG. 3(b), the amount of carbon remaining as free carbon in the finished pellet increases.
還元率が最大となるキルンガス温度は生産量、燃料原単
位、空気比などの操業条件によって微妙に変化する。従
って、常に還元率が最大となるポイントで操業するため
に、キルン排ガス温度を±50℃程度の範囲で定期的に
変化させて、還元率が最大となるキルン排ガス温度を常
に把握しておくことが望ましい。なお、これまでの操業
経験から還元率が最大となるキルン排ガス温度は750
〜850℃の範囲に存在するということができる。The kiln gas temperature at which the reduction rate is maximum varies slightly depending on operating conditions such as production volume, fuel consumption rate, and air ratio. Therefore, in order to always operate at the point where the reduction rate is maximum, it is necessary to periodically change the kiln exhaust gas temperature within a range of about ±50°C and always know the kiln exhaust gas temperature at which the reduction rate is maximum. is desirable. Based on past operating experience, the kiln exhaust gas temperature at which the reduction rate is maximum is 750.
It can be said that it exists in the range of ~850°C.
ちなみに必要水量は、1000℃のキルン排ガスをg
o o ’cまで下げるのに約180fL/を必要であ
り、散水後のガス量は散水前の約7%増となる。By the way, the required amount of water is g of kiln exhaust gas at 1000℃.
Approximately 180 fL/ is required to lower the temperature to o o 'c, and the gas amount after watering is approximately 7% higher than before watering.
なお予熱機2の第1室において、熱交換機あるいは冷風
吸引によってキルン排ガス温度を低下させる方法が考え
られるが、熱交換機を用いることはダスト摩耗の問題や
、設備費が高騰する等の問題を有しているものの有望な
方法の1つと考えられる。冷風吸引による方法は逆にキ
ルン排ガスの02分圧を高め、脱炭を促進する結果とな
り、目的と相反する結果を招くことになる。Note that in the first chamber of the preheater 2, a method of lowering the kiln exhaust gas temperature by using a heat exchanger or cold air suction can be considered, but using a heat exchanger has problems such as dust abrasion and rising equipment costs. This is considered to be one of the most promising methods. On the contrary, the method using cold air suction increases the 02 partial pressure of the kiln exhaust gas and promotes decarburization, which is contrary to the purpose.
〔実施例〕
予熱機第1室内のキルンサイドの天井にキルン軸と直角
に7個のミストスプレーノズル(ノズル仕様50 k
g/ cmX I O41/win 、 ミスト粒滴
径10100pLを50cm間隔で配した。最大散水量
は7017分(生産量15t/時、水量2801/lに
相当)で、散水量は圧力制御方式とした。用いたポンプ
は60 k g / c rn’ X 22kwのプラ
ンジャーポンプである。[Example] Seven mist spray nozzles (nozzle specification 50 k
g/cmX IO41/win, mist droplets with a diameter of 10,100 pL were arranged at intervals of 50 cm. The maximum amount of watering was 7017 minutes (equivalent to a production rate of 15 t/hour and a water amount of 2801/l), and the amount of watering was controlled by pressure. The pump used was a 60 kg/c rn' x 22 kw plunger pump.
本設備を用いて本発明適用効果を調査した。本発明適用
前後者20日間の操業諸元の比較を第2表に示す。The effects of applying the present invention were investigated using this equipment. Table 2 shows a comparison of operating specifications for 20 days before and after application of the present invention.
本発明の適用により還元クロム鉱石ペレットの還元率が
74%から85%まで飛躍的に向上している。また、還
元エネルギーの増加にも拘らず、燃料ガスであるコーク
ス炉ガス原単位は殆ど変化していない。これは予熱機で
のグリーンペレットの脱炭を抑制することが可能となっ
たため、空気比を上げて還元発生COを積極的に燃焼さ
せて排ガス酸素ポテンシャルを高めた操業が可能となっ
たためである。ちなみに排ガス中のCO濃度は本発明の
適用により従来約5%であったものが約2%で操業する
ことが可能となった。By applying the present invention, the reduction rate of reduced chromium ore pellets has been dramatically improved from 74% to 85%. Furthermore, despite the increase in reduction energy, the unit consumption of coke oven gas, which is fuel gas, has hardly changed. This is because it has become possible to suppress the decarburization of green pellets in the preheater, which has made it possible to increase the air ratio and actively burn the CO generated through reduction, making it possible to operate with a higher exhaust gas oxygen potential. . By the way, by applying the present invention, the CO concentration in the exhaust gas, which was conventionally about 5%, has become possible to operate at about 2%.
また、成品ペレットの断面観察から、従来のペレットは
表層部と内部は全く異なる組織を持つ2層構造を呈して
いたが、本発明の適用により表層部、内部ともほぼ均一
な組織となることが判明した。このことから本発明の適
用により、ペレット表層部の還元が内部とほぼ同様に進
行したため、結果としてペレットの組織が粒内でほぼ均
一になったものと考えられる。In addition, from cross-sectional observation of the finished pellet, conventional pellets had a two-layer structure with completely different structures on the surface and inside, but by applying the present invention, it was possible to achieve a nearly uniform structure on both the surface and inside. found. From this, it is considered that by applying the present invention, the reduction of the surface layer of the pellet proceeded almost in the same way as the inside, and as a result, the structure of the pellet became almost uniform within the grain.
これまで還元クロム鉱石ペレットの還元率は最大でも8
0%が限界と考えられていたが、本発明により、90%
台の達成がほぼ可能な域に達した。これにより、転炉の
ステンレス吹錬工程での各種原単位削減、吹錬時間の短
縮による生産性の向上など本発明の有用性は極めて大き
い。Up to now, the reduction rate of reduced chromium ore pellets has been at most 8.
0% was thought to be the limit, but with this invention, 90%
We have reached the point where it is almost possible to achieve this goal. As a result, the usefulness of the present invention is extremely large, such as reducing various basic units in the stainless steel blowing process of a converter and improving productivity by shortening blowing time.
第1図はグレートキルンを用いた還元クロム鉱石ペレッ
トの製造フローシート、第2図は散水後のキルン排ガス
温度と還元率の関係を示すグラフ、第3図(a)は散水
後のキルン排ガス温度と脱炭量/全炭素大量との比、第
3図(b)は散水後のキルン排ガス温度とフリーカーボ
ン/全炭素入量との関係を示すグラフである。
1・・・ディスクペレタイザ
2・・・予熱機
3・・・グレートコンベア
4・・・ロータリーキルン
5・・・クーラ
6・・・バーナ
7・・・スプレーノズルFigure 1 is a production flow sheet for reduced chromium ore pellets using a grate kiln, Figure 2 is a graph showing the relationship between kiln exhaust gas temperature after water sprinkling and reduction rate, and Figure 3 (a) is kiln exhaust gas temperature after water sprinkling. Figure 3(b) is a graph showing the relationship between the temperature of the kiln exhaust gas after water sprinkling and the amount of free carbon/total carbon input. 1...Disc pelletizer 2...Preheater 3...Grate conveyor 4...Rotary kiln 5...Cooler 6...Burner 7...Spray nozzle
Claims (1)
元クロム鉱石ペレットを製造するに際し、ペレットの還
元率に応じて、ロータ リーキルンから予熱機に流入する燃焼排ガス温度を制御
することを特徴とする還元クロム鉱石ペレットの製造方
法。 2 ロータリーキルンから予熱機に流入する燃焼排ガス
温度調節を散水冷却により行うことを特徴とする特許請
求の範囲第1項に記載の還元クロム鉱石ペレットの製造
方法。[Claims] 1. When producing reduced chromium ore pellets in a reduction furnace in which a preheater and a rotary kiln are connected, the temperature of the combustion exhaust gas flowing from the rotary kiln to the preheater is controlled according to the reduction rate of the pellets. A method for producing reduced chromium ore pellets characterized by: 2. The method for producing reduced chromium ore pellets according to claim 1, wherein the temperature of the combustion exhaust gas flowing from the rotary kiln into the preheater is controlled by water cooling.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP27804886A JPS63130730A (en) | 1986-11-21 | 1986-11-21 | Production of reduced chromium ore pellet |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP27804886A JPS63130730A (en) | 1986-11-21 | 1986-11-21 | Production of reduced chromium ore pellet |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS63130730A true JPS63130730A (en) | 1988-06-02 |
JPH0373610B2 JPH0373610B2 (en) | 1991-11-22 |
Family
ID=17591925
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP27804886A Granted JPS63130730A (en) | 1986-11-21 | 1986-11-21 | Production of reduced chromium ore pellet |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63130730A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2017063250A1 (en) * | 2015-10-14 | 2017-04-20 | 福建鼎信实业有限公司 | Production method for hot-delivering oxidized pellets in shaft furnace to sealed ferrochrome electric furnace |
-
1986
- 1986-11-21 JP JP27804886A patent/JPS63130730A/en active Granted
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2017063250A1 (en) * | 2015-10-14 | 2017-04-20 | 福建鼎信实业有限公司 | Production method for hot-delivering oxidized pellets in shaft furnace to sealed ferrochrome electric furnace |
Also Published As
Publication number | Publication date |
---|---|
JPH0373610B2 (en) | 1991-11-22 |
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