JPS628489B2 - - Google Patents
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- Publication number
- JPS628489B2 JPS628489B2 JP54112263A JP11226379A JPS628489B2 JP S628489 B2 JPS628489 B2 JP S628489B2 JP 54112263 A JP54112263 A JP 54112263A JP 11226379 A JP11226379 A JP 11226379A JP S628489 B2 JPS628489 B2 JP S628489B2
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- Prior art keywords
- smelting
- smelting furnace
- solution
- amount
- grade
- 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.)
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Description
本発明は硫化金属鉱中の硫黄対金属比が低下し
た場合でも、該硫化金属鉱の連続製錬を安定して
行なうことを可能ならしめる硫化金属鉱の連続製
錬法に関する。
本出願人はすでに硫化金属鉱の連続製錬法を特
開昭50−15703号公報において開示している。こ
の開示された連続製錬法(以下、従来法という)
は硫化金属鉱と溶剤とを主成分とする溶解原料に
燃料、空気を適宜配合してあらかじめ設定された
反応条件に適応する割合としたものを、溶錬炉の
反応生成物である溶体中に単位時間当り所定の供
給量をもつて直接かつ連続的に装入して溶解させ
て〓と〓を生成せしめ、その際製錬炉で生成する
製錬炉〓を固化粉砕して上記溶錬炉の溶体中に実
質的に連続的に吹送して該製錬炉〓中に含まれた
目的金属の大部分を上記〓に吸収せしめる第一工
程の溶錬工程と溶錬工程における生成物全量を分
離槽に送り〓と〓に分離する第二工程の分離工程
と分離工程からの〓に空気、溶剤、冷剤を適宜配
合し、これを連続的に製錬炉に装入して該〓中の
鉄分及び硫黄分の酸化反応により、目的金属と上
記製錬炉〓とを連続的に生成せしめる第三工程の
製錬工程とよりなり、これらの3工程を連続一貫
して行なうことによつて高い熱効率のもとで、目
的金属を高収率で回収することを可能とするもの
である。
しかるに、最近の鉱石事情、すなわち硫化金属
鉱石、たとえば、銅鉱石は鉱床の変化ならびに選
鉱技術の発達ぬ伴い、S/Cu(重量%)が低下
し、銅品位の上昇が見られる傾向にある。たとえ
ば、ある一種の主要輸入銅鉱石は従来Cu28.5
%、S33.4%、Fe28.6%であつたものがCu31.8
%、S27.2%Fe25.8%と変化している。
また、この硫化金属鉱の連続製錬法は他の製錬
法と比較して鉱石事情の変化に対する適応性にお
いてすぐれているが、きわめて高品位の鉱石処理
の場合、たとえば、原鉱のS/Cuが著しく低下
した場合には原鉱に対する空気あるいは酸素富化
した空気の割合が、目標〓品位を保持するため
に、通常の品位鉱処理の場合より低下することに
なるが、そのため次のごとき問題が発生してい
る。
(1) 鉱石中の鉄分および硫黄分の酸化反応熱が低
下する。
(2) 溶体の撹拌が弱化し、反応効率が低下する。
(3) (2)のために溶体温度の低下が生じ、〓の粘性
が増大し、流動性が悪化する。
(4) 溶体の撹拌力の低下による溶解反応の鈍化お
よび派生的に生ずる溶体の温度低下による粘性
増大のため、スラグロスが増加する。
(5) 上記の溶体温度低下を補うため、バーナ焚き
量が増大する。
(6) バーナ焚き量が増大するため、バーナフレー
ムによる炉壁の溶損が進行し、炉の寿命を短く
する。
(7) 排ガスの温度が上昇し、排ガス系のトラブル
が発生する。
(8) ランス送風量が減少すると、ランス冷却効果
が低下しかつ(5)による炉内雰囲気温度の上昇に
よりランスの消耗が発生し、ランスが消耗して
湯面より離れると、上記(1)〜(7)の現象が送風量
の正常な場合でも起こる。
このように、従来法はきわめて高品位の硫化金
属鉱処理には有効に適応できず、硫化金属鉱の連
続製錬を安定して行なうことは困難であつた。
第5図は硫化金属鉱として銅精鉱を用いる場
合、〓品位を65%とするための銅精鉱中の銅品位
と硫黄品位の下限との関係を示すグラフ図であ
る。この場合の上記溶錬炉で生成される〓は
Cu2SとFeSとからなる中間生成物であり、従つ
て〓品位に関与する硫黄量は必要であるが、酸化
反応熱に関与する硫黄量は流動性固体燃料、たと
えば粉炭中の炭素と水素で代替させることができ
る。通常の〓品位は65%を目標値としているの
で、それに見合つた〓中の硫黄は22%である。
いま、〓の銅品位65%、銅精鉱中の銅品位30%
と仮定すると、第5図に示すように、10.15の硫
黄品位で操業可能である。たとえば、〓品位5%
で銅精鉱中の銅品位28〜32%の場合、銅精鉱中の
硫黄品位の下限は第5図に示す範囲である。それ
以下の硫黄品位の場合は〓品位を上げなければな
らない。
本発明は上記の従来法の欠点を解決し、硫化金
属鉱中の硫黄と金属比が低下した場合でも、該硫
化金属鉱の連続製錬を安定して行なうことを可能
ならしめる硫化金属鉱の連続製錬法を提供するも
ので、その要旨とするところは、硫化金属鉱と溶
剤との混合物からなる原料に空気と流動性固体燃
料を適宜配合し、これを連続的に溶錬炉に装入し
溶解せしめて〓と〓を生成させ、その際製錬炉か
らの製錬炉〓を固化粉砕して連続的に該溶錬炉に
装入して該製錬炉〓中に含有された目的金属の大
部分を上記〓中に吸収せしめる溶錬工程と該溶錬
工程の生成物を金属分離槽に移送して〓と〓とに
分離する分離工程と該分離工程からの〓に溶剤と
空気を適宜配合し、これを連続的に該製錬炉に装
入し、目的金属と上記製錬炉〓とを生成する製錬
工程とよりなる硫化金属鉱の連続製錬法におい
て、あらかじめ該溶錬工程の溶錬炉に装入する上
記原料の溶解を促進するに足る溶体の所要撹拌を
確保するための最低送風量を操業条件に応じて設
定しておき、該溶錬炉に装入される硫化金属鉱品
位および該溶錬炉で生成される〓及び〓の品位に
基づいて目標〓品位を保持すべく計算された酸化
用送風量とともに、該硫化金属鉱品位に対応して
該最低送風量保持に必要な補充空気とそれに見合
う流動性固体燃料をランスを介して直接上記溶体
内に吹送し、かつ該製錬工程の製錬炉内の溶体中
の鉄分、硫黄分等の被酸化成分の効果的な酸化と
該溶体内のより急速な熱伝達に必要な該溶体の所
要撹拌を確保するための最低送風量を該製錬炉に
装入される〓品位及び空気中の酸素量に応じて設
定しておき、上記分離槽からの〓の成分及び量、
冷剤の成分および量等に基づいて計算された酸化
用送風量とともに該〓品位に対応して該最低送風
量の保持に必要な補充空気量とそれに見合う流動
性固体燃料をランスを介して直接上記溶体内に吹
送することを特徴とする硫化金属鉱の連続製錬
法、にある。
次に本発明を図によつて説明する。
本発明において使用される流動性固体燃料は粉
状の固体燃料であればよく、石炭、木炭、コーク
ス、ノコ屑、固体炭素、硫黄、プラスチツク、ゴ
ム等を含む。以下、硫化金属鉱として銅精鉱を、
また流動性固体燃料として粉炭をそれぞれ使用す
る場合について述べる。
第1図は本発明の一実施例の溶錬工程における
システムフロー図、第2図は第1図の溶錬工程に
おける銅精鉱と溶剤と粉炭の装入設備の概略図、
第3図は第1図の溶錬工程の溶錬炉の断面図、第
4図は第1図の実施例の製錬工程の製銅炉の断面
図、第6図は第1図の溶錬工程において銅精鉱給
鉱量25T/hr、生成〓品位65%、80%酸素2500N
m3/hr、3インチランス5本使用時の銅精鉱中の
S/Cuとランス風速、重油量との関係を示すグ
ラフ図である。
まず、本発明の溶錬工程について述べる。
第1図において、溶錬工程の溶錬炉に装入され
る銅精鉱品位、溶剤品位及び溶錬炉で生成する〓
および〓の品位に基づいて、銅精鉱トン当りの反
応必要酸素量及び必要溶剤量が計算され、物量デ
ータ収集後、送風量計算および温度制御計算がな
されて送風量びバーナ重油量が決定される。本発
明は溶錬炉で生成する〓の品位を目標〓品位に保
持するために、上記送風量計算値、すなわち酸化
用送風量があらかじめ設定してある最低送風量を
下廻る場合には上記酸化用送風量とともに該硫化
金属鉱品位の上昇度に対応して該最低速風量保持
するに必要な補充空気量とそれに見合う粉炭を直
接溶体内に装入するシステムである。
上記あらかじめ設定してある最低送風量とは溶
錬炉内の溶体撹拌が充分行なわれ、溶錬炉内に装
入される原料の溶解が充分促進されうる空気量で
あり、この最低空気量を操業条件に応じて設定し
ておくのである。
いま、上記のごとき鉱石事情により、銅精鉱中
のS/Cuが低下し、高銅品位の銅精鉱を処理す
る場合は該S/Cuの低下により上記送風量計算
値すなわち酸化用送風量があらかじめ設定してお
いた最低送風量を下廻る場合には上記酸化用送風
量とともに該硫化金属鉱品位の上昇度に対応して
上記のように常時その最低送風量保持するに必要
な補充空気量とそれに見合う粉炭が装入されるの
である。この装入される粉炭は上記のように物量
データ収集され、熱計算されて、それに対応して
バーナ重油量は減少される。この場合の重油、粉
炭、銅精鉱中の硫黄の発熱量、有効発熱量、燃焼
空気量の関係は次の表に示される通りである。
The present invention relates to a method for continuous smelting of sulfide metal ores, which allows continuous smelting of sulfide metal ores to be carried out stably even when the sulfide to metal ratio in the sulfide metal ores decreases. The present applicant has already disclosed a continuous smelting method for metal sulfide ore in Japanese Patent Application Laid-Open No. 15703/1983. This disclosed continuous smelting method (hereinafter referred to as the conventional method)
is a melted raw material whose main components are metal sulfide ore and a solvent, mixed with fuel and air in proportions that suit preset reaction conditions, into a solution that is a reaction product of a smelting furnace. A predetermined amount of supply per unit time is directly and continuously charged and melted to produce 〓 and 〓, and at that time, the smelting furnace 〓 produced in the smelting furnace is solidified and pulverized to the above-mentioned smelting furnace. The total amount of products in the smelting process and the smelting process of the first step in which most of the target metal contained in the smelting furnace is absorbed into the smelting furnace by substantially continuous blowing into the solution. Air, solvent, and coolant are appropriately mixed with the separation process of the second step, which is sent to the separation tank and separated into 〓 and 〓, and the 〓 from the separation process is continuously charged into the smelting furnace. The third step is a smelting step in which the target metal and the above-mentioned smelting furnace are continuously produced by the oxidation reaction of iron and sulfur. This makes it possible to recover target metals in high yields with high thermal efficiency. However, due to the recent ore situation, that is, sulfide metal ores, such as copper ores, there is a tendency for S/Cu (weight %) to decrease and copper grade to increase due to changes in ore deposits and the lack of development in ore beneficiation technology. For example, one type of major imported copper ore is traditionally Cu28.5
%, S33.4%, Fe28.6% is Cu31.8
%, S27.2% Fe25.8%. In addition, this continuous smelting method for metal sulfide ores has superior adaptability to changes in ore conditions compared to other smelting methods, but in the case of extremely high-grade ore processing, If Cu is significantly reduced, the ratio of air or oxygen-enriched air to the raw ore will be lower than in normal grade ore processing in order to maintain the target grade. A problem is occurring. (1) The heat of oxidation reaction of iron and sulfur in the ore decreases. (2) Stirring of the solution is weakened, reducing reaction efficiency. (3) Due to (2), the solution temperature decreases, the viscosity of the solution increases, and the fluidity deteriorates. (4) Slag loss increases due to the slowdown of the dissolution reaction due to a decrease in the stirring power of the solution and the subsequent increase in viscosity due to the decrease in temperature of the solution. (5) To compensate for the above drop in solution temperature, the amount of burner firing increases. (6) As the amount of burner firing increases, the burner frame causes further erosion of the furnace wall, shortening the life of the furnace. (7) The exhaust gas temperature rises, causing problems with the exhaust gas system. (8) When the lance air flow rate decreases, the lance cooling effect decreases and the lance wears out due to the increase in the furnace atmosphere temperature due to (5). The phenomena described in ~(7) occur even when the airflow rate is normal. As described above, conventional methods cannot be effectively applied to the treatment of extremely high-grade metal sulfide ores, and it has been difficult to stably and continuously smelt metal sulfide ores. FIG. 5 is a graph showing the relationship between the copper grade in the copper concentrate and the lower limit of the sulfur grade in order to set the grade to 65% when copper concentrate is used as the metal sulfide ore. In this case, the 〓 produced in the above smelting furnace is
It is an intermediate product consisting of Cu 2 S and FeS, and therefore the amount of sulfur involved in the grade is necessary, but the amount of sulfur involved in the heat of oxidation reaction is due to the amount of sulfur involved in the heat of oxidation reaction, which is due to the carbon and hydrogen in fluid solid fuels, such as powdered coal. It can be replaced with . The standard target value for grain quality is 65%, so the sulfur content in the grain is 22%. Currently, the copper grade of 〓 is 65%, and the copper grade of copper concentrate is 30%.
Assuming that, as shown in Figure 5, it is possible to operate with a sulfur grade of 10.15. For example, = quality 5%
When the copper grade in the copper concentrate is 28 to 32%, the lower limit of the sulfur grade in the copper concentrate is in the range shown in FIG. If the sulfur grade is lower than that, the grade must be increased. The present invention solves the above-mentioned drawbacks of the conventional method, and produces a sulfide metal ore that enables stable continuous smelting of the sulfide metal ore even when the sulfur to metal ratio in the sulfide metal ore decreases. It provides a continuous smelting method, and its gist is to mix air and fluid solid fuel appropriately with a raw material consisting of a mixture of sulfide metal ore and a solvent, and to continuously load this into a smelting furnace. In this case, the smelting furnace 〓 from the smelting furnace is solidified and crushed and continuously charged into the smelting furnace to be contained in the smelting furnace. A smelting process in which most of the target metal is absorbed into the above-mentioned metal, a separation process in which the product of the smelting process is transferred to a metal separation tank and separated into two, and a solvent is added to the liquid from the separation process. In the continuous smelting method for sulfide metal ore, which comprises a smelting process in which air is appropriately blended and continuously charged into the smelting furnace to produce the target metal and the smelting furnace, In order to ensure the required stirring of the solution to promote the melting of the raw material charged into the smelting furnace in the smelting process, the minimum air flow rate is set according to the operating conditions, and the raw material is charged into the smelting furnace. In addition to the oxidizing air flow rate calculated to maintain the target grade based on the grade of sulfide metal ore produced in the smelting furnace and the grade of 〓 and 〓 produced in the smelting furnace, the minimum The supplementary air necessary to maintain the air flow rate and the corresponding fluid solid fuel are blown directly into the solution through a lance, and the iron, sulfur, etc. in the solution in the smelting furnace of the smelting process are oxidized. The grade and amount of oxygen in the air charged to the smelting furnace to ensure the required agitation of the solution necessary for effective oxidation of the components and more rapid heat transfer within the solution. The ingredients and amount of 〓 from the above separation tank,
In addition to the oxidizing air flow rate calculated based on the composition and amount of the refrigerant, the amount of replenishment air necessary to maintain the minimum air flow rate corresponding to the grade and the corresponding fluid solid fuel are directly delivered via the lance. A continuous smelting method for sulfide metal ore, characterized by blowing into the solution. Next, the present invention will be explained with reference to the drawings. The fluid solid fuel used in the present invention may be any solid fuel in powder form, and includes coal, charcoal, coke, sawdust, solid carbon, sulfur, plastic, rubber, and the like. Below, copper concentrate is used as sulfide metal ore,
We will also discuss the use of powdered coal as a fluid solid fuel. Fig. 1 is a system flow diagram in the smelting process of an embodiment of the present invention, Fig. 2 is a schematic diagram of the copper concentrate, solvent, and powdered coal charging equipment in the smelting process of Fig. 1;
3 is a sectional view of the smelting furnace in the smelting process shown in FIG. In the refining process, copper concentrate feed amount is 25T/hr, production grade is 65%, 80% oxygen is 2500N
FIG . 3 is a graph showing the relationship between S/Cu in copper concentrate, lance wind speed, and amount of heavy oil when m 3 /hr and five 3-inch lances are used. First, the smelting process of the present invention will be described. In Figure 1, the grade of copper concentrate charged into the smelting furnace in the smelting process, the grade of the solvent, and the amount produced in the smelting furnace
Based on the grades of and 〓, the amount of oxygen required for reaction and the amount of solvent required per ton of copper concentrate are calculated, and after collecting the physical quantity data, the amount of air flow and temperature control are calculated to determine the amount of air flow and burner heavy oil. Ru. In order to maintain the quality of 〓 produced in the smelting furnace at the target 〓 grade, the oxidation This system directly charges into the solution the amount of replenishing air necessary to maintain the minimum speed of air flow and the amount of powdered coal corresponding to the air flow rate in accordance with the degree of increase in the grade of the metal sulfide ore. The above preset minimum air flow rate is the amount of air that can sufficiently stir the solution in the smelting furnace and sufficiently promote the melting of the raw materials charged into the smelting furnace. It is set according to the operating conditions. Now, due to the above-mentioned ore circumstances, the S/Cu in copper concentrate is decreasing, and when processing high copper grade copper concentrate, due to the decrease in S/Cu, the above calculated air flow rate, that is, the air flow rate for oxidation, is lowered. If the air flow rate is lower than the preset minimum air flow rate, in addition to the above-mentioned oxidation air flow rate, supplementary air necessary to maintain the minimum air flow rate at all times as described above will be added in accordance with the degree of increase in the grade of the metal sulfide ore. The appropriate amount of powdered coal is charged. Quantity data of the charged pulverized coal is collected as described above, thermal calculation is performed, and the amount of burner heavy oil is correspondingly reduced. In this case, the relationship between the calorific value of sulfur in heavy oil, powdered coal, and copper concentrate, effective calorific value, and amount of combustion air is as shown in the following table.
【表】
上表の有効発熱量とは炉内で理論空気量を用い
て燃焼させた燃料の発熱量から排ガスとして1250
℃で出た場合の該排ガスの持ち去る熱量を差し引
いた炉内で有効に働く発熱量である。
第2図は粉炭装入設備である。図において、1
は乾燥された粉炭のホツパ、2はベルトフイダ
ー、3はウエイヤー、4はシユート、5は輸送チ
エンコンベヤである。上記のように計算された粉
炭量がホツパ1よりベルトフイダー2によつて切
り出され、ウエイヤー3で計量後、シユート4を
径て輸送チエンコンベヤ5に入り、溶錬炉頂装入
設備まで運搬される。銅精鉱、溶剤についても同
様である。
第3図は溶錬炉の断面図である。図において、
6はランス、7はバーナ、8は溶体流出孔、9は
波止、10は溶体である。溶錬炉では鉱石(銅精
鉱)珪酸塩等の溶剤を主成分とする原料に粉炭お
よび空気を予定した反応条件に適する割合で適宜
配合したものを所定の供給速度で炉内の反応生成
物である溶体10中に直接かつ連続的に装入す
る。その際、粉炭は第2図および第3図に示すよ
うに、原料と同じランス6を用いて原料とともに
溶体10中に直接供給してもよく、また粉炭専用
ランスにより別に溶体10中に直接吹送してもよ
い。溶体10内に供給された粉炭は通常は炉内に
て完全に燃焼するが、過剰に供給された場合は未
燃粉炭が溶体10上に浮遊し、溶体流出孔8から
流出することがある。そのため、炉の溶体出口に
波止3を取り付けることにより未燃粉炭の炉外へ
の流出を抑えることができ、未燃粉炭はやがて炉
内で燃焼しつくす。
第6図は銅精鉱給鉱量25T/hr、生成〓品位65
%、80%酸素2500Nm3/hr、3インチランス5本
使用時の銅精鉱中のS/Cuとランス風速、重油
量との関係を示すグラフである。ランス風速は次
の式で求められる。
ランス風速=ランス1本当りの(送風量
+酸素量)/(3600秒×0.005m2)
たとえば、従来ランス1本当り3300Nm3/hrの
送風量であつたが、〓品位の上昇により新たに計
算された時点で2700Nm3/hrに減少した場合、す
なわちランス風速が180m/secから150m/secに
低下した場合には銅鉱石給鉱量を一定に保持する
ためには、溶体酸化反応熱の減少を外部からの加
熱で補充しなければならない。この際、外部から
の熱補充は、たとえば通常のバーナから行なつた
場合には、ランス風速の低下に伴つて生ずる溶体
の撹拌現象の減少によつて溶体へのバーナ発生熱
の伝達率が低下し溶体の温度が下り、原料装入物
の溶解が有効に促進されないことが発生した。銅
鉱石中のS/Cuが低下した場合、所定の溶体撹
拌を得るための送風量を常時供給すると、〓品位
は上昇しつづけることから、上記普通銅精鉱操業
時、たとえばS/Cuが1.1の場合の給鉱停止等の
理由により、〓品位上昇の場合も短期的には同じ
レベルで考えて差支えない。
第6図において、たとえば最低ランス風速150
m/sec、すなわち最低送風量11000Nm3/hrに設
定値を合わせると、銅鉱石中のS/Cuが0.9の場
合には送風量が3100Nm3/hr不足となる。上表か
ら、その最低送風量を保持するのに必要な補充空
気量見合いの粉炭量は408Kgである。粉炭量408
Kg/hrの発熱量は1346000Kcalであり、その発熱
量見合いの重油369が節減できる。これはモデ
ル計算値であるが、実操業においては〓品位が変
動し、また銅鉱石のS/Cuも異なるため、鉱石
トン当りの必要酸素量が増減し、それに合わせて
設定した最低送風量に基づいて粉炭装入量も増減
する。さらに、設定最低送風量は任意に設定可能
であり、設定値を上げることにより、ランス送風
量の許される範囲において任意に粉炭の用が可能
となる。
本発明は上述したように、粉炭を溶体中に直接
吹送するために、従来のバーナ加熱方式に比べて
溶体への熱伝達がよくなり、かつ溶体の撹拌が十
分行なわれるため溶解能力が向上し、溶体の流動
性も良くなるため生成物の炉外の流出もスムーズ
に行なわれ、同時に撹拌により〓と〓の接触が十
分行なわれ、懸遊している〓粒子は容易に粗粒化
し、沈降し、〓中の銅損失は少なくなる。また、
燃焼熱の溶体への伝達がよくなるため、炉内ガス
ゾーンの雰囲気温度と溶体との温度差を小さくで
きかつバーナ焚き量が減少する結果、バーナフレ
ームによつて溶損される炉壁の寿命が著しく延長
される。さらに、排ガスの温度を溶体の温度とほ
ぼ同一の温度まで低下させることができるので、
排ガスの後処理上きわめて有利である。上記粉炭
のランス吹込みは従来の重油バーナ設備を全く変
更することなく、実施することができ、しかも重
油の使用量の節減を可能ならしめるものであり、
この燃料源の粉炭への一部転換は現在の世界石油
事情からもきわめて意義あるものである。
次に、本発明の製錬工程について述べる。
製錬工程においても製銅炉への粉炭ランス吹込
みは上記の溶錬炉の場合と同様に実施することが
できる。
第4図は第3図の溶錬炉に対応する製銅炉の断
面図である。図において、11はランス、12は
分離工程からの〓入口、13はバーナ、14は粗
銅出口、15は製銅炉〓出口、16は溶体であ
る。すなわち、製錬工程の製銅炉内の溶体16中
の鉄分、硫黄分等の被酸化成分の効果的な酸化と
溶体16内のより急速な熱伝達に必要な溶体16
の所要撹拌とを確保するための最低送風量を該製
銅炉に〓入口12から装入される〓品位及び空気
中の酸素量に応じて設定しておき、上記分離槽か
らの〓の成分及び量、冷剤の成分及び量等に基づ
いて計算された酸化用送風量が〓装入量が減じた
場合、あるいは製銅炉酸化過剰の場合等に上記設
定量低送風量を下廻る場合には、該酸化用送風量
とともに該最低送風量の保持に必要な補充空気量
とそれに見合う粉炭をランス11を介して直接上
記溶体16内に吹送する。その際、発生する過剰
熱量は目的金属のスクラツプ等の冷剤の装入溶解
に使用され、全体の鉱石処理能力を増大させるこ
とを可能とする。さらに進めて、目的金属のスク
ラツプ等の冷剤装入溶解を行ない、全体の鉱石処
理能力を増大させるために、粉炭を装入制御する
ことができる。
以上において、硫化金属鉱が硫化銅である場合
の本発明について述べたが、ニツケル、コバルト
等の硫化鉱石の場合にも、本発明は適用できるこ
とはもろちろんである。
本発明は、以上のように、硫化金属鉱品位上昇
の場合でも、溶錬炉および製錬炉における炉内溶
体の有効な撹拌をつねに可能ならしめるように、
上吹きランスを介しての流動性固体燃料の溶体内
への直接吹送を制御することによつて、目的金属
を安定して大量かつ経済的に製造することを可能
ならしめる硫化金属鉱の連続製錬法を提供するも
ので、その工業的価値はきわめて高い。
次に、本発明を実施例によつて具体的に説明す
るが、本発明はその要旨を越えない限り以下の実
施例に限定されるものではない。
実施例
溶錬工程の溶錬炉にそれぞれ毎時銅29.73%、
硫黄29.63%、鉄24.97%、珪酸6.58%よりなる銅
精鉱24.4T、珪砂3.4T、石灰0.1Tをゲージ圧2
Kg/cm2の最低送風量設定値11700Nm3/hrの空
気、2240Nm3/hrの酸素ガスとともにランスを通
じて溶錬炉内の反応生成物である溶体中に直接吹
送した。これら銅精鉱、珪砂、石灰はそれぞれ粒
径3m/m以下で水分1%以下まで乾燥したもの
を用い、ランスは3インチパイプ(内径80.1m/
m)5本を使用し、ランス内の流速は155m/sec
であつた。このように、溶錬炉に装入される硫化
金属鉱品位および該溶錬炉で生成される〓および
〓の品位に基いて目標〓品位を保持すべく計算さ
れた酸化用送風量が上記最低送風量を下廻る場合
には、該酸化用送風量とともに、最低送風量保持
11700Nm3/hrに対し、最低送風量保持に必要な
補充空気量とそれに見合う粉炭873Kg/hrがラン
スを介して同じく溶体内に直接吹送された。それ
によつて、バーナ重油は1400/hrから931/
hrに減少し、溶体温度は1188℃から1213℃まで上
昇した。
溶錬炉で生成した〓と〓を全量次の分離工程の
分離槽に移送して〓と〓とに分離した。
次に、製錬工程の製銅炉にそれぞれ毎時分離槽
からの銅64.9%、硫黄21.83%、鉄9.91%からなる
〓11.5T、石灰0.7Tをゲージ圧2Kg/cm2の8240N
m3/hrの空気、1000Nm3/hrの80%酸素ガスとと
もに3インチランス4本を介して製銅炉内の反応
生成物である溶体内に直接吹送した。製銅炉内の
熱バランスは平衡を保つた状態にあり、バーナ重
油量はゼロになり、溶体温度1230℃で、製銅炉〓
中の銅は16%であつた。
送風量を最低送風量設定値10000Nm3/hrにし
たところ、過剰空気に見合う粉炭230Kg/hrがラ
ンスを介して吹送され、過剰熱量見合いのアノー
ド残基を4100Kg/hr装入することができた。溶体
温度は1230℃で製銅炉〓の銅は15%であつた。[Table] The effective calorific value in the table above is calculated from the calorific value of the fuel combusted in the furnace using the theoretical amount of air.
This is the amount of heat that effectively works in the furnace after subtracting the amount of heat carried away by the exhaust gas when it exits at ℃. Figure 2 shows the pulverized coal charging equipment. In the figure, 1
2 is a belt feeder, 3 is a weyer, 4 is a chute, and 5 is a transport chain conveyor. The amount of pulverized coal calculated as above is cut out from the hopper 1 by the belt feeder 2, weighed by the weir 3, then enters the transport chain conveyor 5 through the chute 4, and is transported to the top charging equipment of the smelting furnace. . The same applies to copper concentrate and solvent. FIG. 3 is a sectional view of the smelting furnace. In the figure,
6 is a lance, 7 is a burner, 8 is a solution outflow hole, 9 is a wharf, and 10 is a solution. In the smelting furnace, a mixture of powdered coal and air in a proportion appropriate to the planned reaction conditions is added to the raw material whose main component is a solvent such as ore (copper concentrate) and silicate, and the reaction products in the furnace are fed at a predetermined feeding rate. directly and continuously into the solution 10. At that time, as shown in FIGS. 2 and 3, the powdered coal may be directly fed into the solution 10 together with the raw material using the same lance 6 as the raw material, or it may be directly blown into the solution 10 using a lance exclusively for powdered coal. You may. The pulverized coal supplied into the solution 10 is normally completely combusted in the furnace, but if excessively supplied, unburned pulverized coal may float on the solution 10 and flow out from the solution outlet hole 8. Therefore, by attaching the wharf 3 to the melt outlet of the furnace, it is possible to prevent the unburned coal from flowing out of the furnace, and the unburned coal will eventually burn out inside the furnace. Figure 6 shows copper concentrate feed amount 25T/hr, production = grade 65
%, 80% oxygen at 2500 Nm 3 /hr, and five 3-inch lances are used. It is a graph showing the relationship between S/Cu in copper concentrate, lance wind speed, and amount of heavy oil. The lance wind speed is calculated using the following formula. Lance air speed = (air volume + oxygen volume) / (3600 seconds x 0.005 m2 ) In order to keep the amount of copper ore feed constant, if the lance wind speed decreases to 2700Nm 3 /hr at the calculated time, that is, if the lance wind speed decreases from 180m/sec to 150m/sec, the solution oxidation reaction heat must be The reduction must be supplemented with external heating. At this time, if external heat supplementation is performed from a normal burner, for example, the rate of transfer of heat generated by the burner to the solution decreases due to the decrease in the stirring phenomenon of the solution that occurs as the lance wind speed decreases. However, the temperature of the solution decreased and the melting of the raw material charge was not effectively promoted. When the S/Cu in the copper ore decreases, if the amount of air blowing to obtain the prescribed solution stirring is constantly supplied, the grade will continue to rise. Due to reasons such as suspension of ore supply in cases of In Figure 6, for example, the minimum lance wind speed is 150
m/sec, that is, the minimum air flow rate of 11000 Nm 3 /hr, if S/Cu in the copper ore is 0.9, the air flow rate will be insufficient by 3100 Nm 3 /hr. From the table above, the amount of powdered coal corresponding to the amount of supplementary air required to maintain the minimum air flow rate is 408 kg. Powdered coal amount 408
The calorific value per kg/hr is 1,346,000 Kcal, and the equivalent amount of heavy oil can be saved by 369 kg. This is a model calculation value, but in actual operation, the grade changes and the S/Cu of copper ore varies, so the amount of oxygen required per ton of ore increases or decreases, and the minimum air flow rate set accordingly Based on this, the amount of pulverized coal charged will also be increased or decreased. Further, the set minimum air flow rate can be set arbitrarily, and by increasing the set value, it becomes possible to use pulverized coal arbitrarily within a range that allows the lance air flow rate. As described above, the present invention blows powdered coal directly into the solution, which improves heat transfer to the solution compared to conventional burner heating methods, and improves melting ability because the solution is sufficiently stirred. Since the fluidity of the solution improves, the product can flow out of the furnace smoothly, and at the same time, the stirring ensures sufficient contact between the solution and the solution, and the suspended particles easily become coarse and settle. However, the copper loss in the middle will be reduced. Also,
Since the transfer of combustion heat to the solution is improved, the temperature difference between the ambient temperature in the furnace gas zone and the solution can be reduced, and the amount of burner firing is reduced.As a result, the life of the furnace wall, which is eroded by the burner flame, is shortened. significantly extended. Furthermore, the temperature of the exhaust gas can be lowered to almost the same temperature as the solution temperature.
This is extremely advantageous in terms of after-treatment of exhaust gas. The above-mentioned lance injection of powdered coal can be carried out without any changes to conventional heavy oil burner equipment, and it is possible to reduce the amount of heavy oil used.
This partial conversion to pulverized coal as a fuel source is extremely significant considering the current global oil situation. Next, the smelting process of the present invention will be described. In the smelting process as well, powdered coal lance injection into the copper making furnace can be carried out in the same manner as in the case of the above-mentioned smelting furnace. FIG. 4 is a sectional view of a copper making furnace corresponding to the smelting furnace of FIG. 3. In the figure, 11 is a lance, 12 is an inlet from the separation process, 13 is a burner, 14 is a blister copper outlet, 15 is a copper furnace outlet, and 16 is a solution. That is, the solution 16 is necessary for effective oxidation of oxidized components such as iron and sulfur in the solution 16 in the copper furnace in the smelting process and for more rapid heat transfer within the solution 16.
The minimum amount of air flow to ensure the required agitation of If the oxidizing air flow rate calculated based on the composition and amount of the refrigerant is lower than the above-mentioned set low air flow rate due to a decrease in the charging amount or excessive oxidation in the copper making furnace, etc. In addition to the oxidizing air flow rate, supplementary air volume necessary to maintain the minimum air flow rate and powdered coal commensurate with the supplementary air volume are blown directly into the solution 16 through the lance 11. In this case, the excess heat generated is used for charging and melting a coolant such as scrap of the target metal, making it possible to increase the overall ore processing capacity. Further, controlled charging of pulverized coal can be performed to perform coolant charging melting of target metal scrap or the like to increase overall ore processing capacity. Although the present invention has been described above in the case where the sulfide metal ore is copper sulfide, it goes without saying that the present invention is also applicable to sulfide ores such as nickel and cobalt. As described above, the present invention enables effective stirring of the in-furnace solution in the smelting furnace and the smelting furnace even when the grade of sulfide metal ore increases.
Continuous production of sulfide metal ore that enables the stable, large-scale, and economical production of target metals by controlling the direct blowing of a fluid solid fuel into a solution through a top-blown lance. It provides a method of alchemy, and its industrial value is extremely high. EXAMPLES Next, the present invention will be specifically explained using Examples, but the present invention is not limited to the following Examples unless the gist of the invention is exceeded. Example: 29.73% copper per hour in the smelting furnace of the smelting process,
24.4T copper concentrate consisting of 29.63% sulfur, 24.97% iron, and 6.58% silicic acid, 3.4T silica sand, and 0.1T lime at a gauge pressure of 2
Air was blown at a minimum blowing rate of 11,700 Nm 3 /hr and oxygen gas was blown through a lance directly into the solution , which was a reaction product, in the smelting furnace. These copper concentrate, silica sand, and lime are each dried to a particle size of 3 m/m or less and a moisture content of 1% or less, and the lance is a 3 inch pipe (inner diameter 80.1 m/m).
m) Using 5 lances, the flow velocity inside the lance is 155m/sec.
It was hot. In this way, the oxidizing air flow rate calculated to maintain the target grade based on the grade of sulfide metal ore charged into the smelting furnace and the grades of If the airflow rate is lower than the airflow rate, maintain the minimum airflow rate in addition to the oxidation airflow rate.
For 11,700 Nm 3 /hr, the amount of supplementary air necessary to maintain the minimum air flow rate and the corresponding amount of powdered coal of 873 kg/hr were also blown directly into the solution via a lance. As a result, burner heavy oil will be reduced from 1400/hr to 931/hr.
hr, and the solution temperature increased from 1188℃ to 1213℃. The entire amount of 〓 and 〓 produced in the smelting furnace was transferred to a separation tank for the next separation step and separated into 〓 and 〓. Next, 11.5T and 0.7T of lime, each consisting of 64.9% copper, 21.83% sulfur, and 9.91% iron, are added to the copper furnace in the smelting process from the separation tank every hour at 8240N at a gauge pressure of 2Kg/ cm2.
It was blown directly into the solution, which is a reaction product, in a copper making furnace through four 3-inch lances together with air at m 3 /hr and 80% oxygen gas at 1000 Nm 3 /hr. The heat balance inside the copper making furnace is in equilibrium, the amount of burner heavy oil is zero, the solution temperature is 1230℃, and the copper making furnace is in equilibrium.
The copper content inside was 16%. When the air flow rate was set to the minimum air flow setting value of 10,000Nm 3 /hr, 230Kg/hr of powdered coal was blown through the lance to compensate for the excess air, and 4,100Kg/hr of anode residue was charged to compensate for the excess heat. . The solution temperature was 1230°C and the copper content in the copper making furnace was 15%.
第1図は本発明の一実施例の溶錬工程における
システムフロー図、第2図は第1図の溶錬工程に
おける銅精鉱と溶剤と粉炭の装入設備の概略図、
第3図は第1図の溶錬工程の溶錬炉の断面図、第
4図は第1図の実施例の製錬工程の製銅炉の断面
図、第5図は硫化金属鉱として銅精鉱を用いる場
合、〓品位を65%とするための銅精鉱中の銅品位
と硫黄品位の下限との関係を示すグラフ図、第6
図は第1図の溶錬工程において銅精鉱給鉱量
25T/hr、生成〓品位65%、80%酸素2500Nm3/
hr、3インチランス5本使用時の銅精鉱中のS/
Cuとランス風速、重油量との関係を示すグラフ
図である。第2図、第3図および第4図におい
て、
1……粉炭ホツパ、2……ベルトフイダー、3
……ウエイヤー、4……シユート、5……輸送チ
エンコンベヤ、6,11……ランス、7,13…
…バーナ、8……溶体流出孔、9……波止、1
0,16……溶体、12……〓入口、14……粗
銅出口、15……製銅炉〓出口。
Fig. 1 is a system flow diagram in the smelting process of an embodiment of the present invention, Fig. 2 is a schematic diagram of the copper concentrate, solvent, and powdered coal charging equipment in the smelting process of Fig. 1;
Figure 3 is a cross-sectional view of the smelting furnace in the smelting process shown in Figure 1, Figure 4 is a cross-sectional view of the copper making furnace in the smelting process of the embodiment shown in Figure 1, and Figure 5 shows copper as sulfide metal ore. When using concentrate, Graph diagram showing the relationship between the copper grade and the lower limit of sulfur grade in copper concentrate to make the grade 65%, No. 6
The figure shows the amount of copper concentrate fed in the smelting process in Figure 1.
25T/hr, production = grade 65%, 80% oxygen 2500Nm 3 /
hr, S/ in copper concentrate when using five 3-inch lances
It is a graph diagram showing the relationship between Cu, lance wind speed, and amount of heavy oil. In Figures 2, 3, and 4, 1...pulverized coal hopper, 2...belt feeder, 3
...Wayer, 4...Chute, 5...Transportation chain conveyor, 6,11...Lance, 7,13...
... Burner, 8 ... Solution outflow hole, 9 ... Wharf, 1
0,16...solution, 12...=inlet, 14...blister copper outlet, 15...coppermaking furnace=outlet.
Claims (1)
空気と流動性固体燃料を適宜配合し、これを連続
的に溶錬炉に装入し溶解せしめて〓と〓を生成さ
せ、その際製錬炉からの製錬炉〓を固化粉砕して
連続的に該溶錬炉に装入して該製錬炉〓中に含有
された目的金属の大部分を上記〓中に吸収せしめ
る溶錬工程と該溶錬工程の生成物を全量分離槽に
移送して〓と〓とに分離する分離工程と該分離工
程からの〓に溶剤と空気を適宜配合し、これを連
続的に該製錬炉に装入し、目的金属と上記製錬炉
〓とを生成する製錬工程とよりなる硫化金属鉱の
連続製錬法において、あらかじめ該溶錬工程の溶
錬炉に装入する上記原料の溶解を促進するに足る
溶体の所要撹拌を確保するための最低送風量を操
業条件に応じて設定しておき、該溶錬炉に装入さ
れる硫化金属鉱品位および該溶錬炉で生成される
〓及び〓の品位に基づいて目標〓品位を保持すべ
く計算された酸化用送風量とともに該硫化金属鉱
品位に対応して該最低送風量保持に必要な補充空
気量とそれに見合う流動性固体燃料をランスを介
して直接上記溶体内に吹送し、かつ該製錬工程の
製錬炉内の溶体中の鉄分、硫黄分等の被酸化成分
の効果的な酸化と該溶体内のより急速な熱伝達に
必要な該溶体の所要撹拌を確保するための最低送
風量を該製錬炉に装入される〓品位及び空気中の
酸素量に応じて設定しておき、上記分離槽からの
〓の成分及び量、冷剤の成分及び量等に基づいて
計算された酸化用送風量とともに該〓品位に対応
して該最低送風量の保持に必要な補充空気量とそ
れに見合う流動性固体燃料をランスを介して直接
上記溶体内に吹送することを特徴とする硫化金属
の連続製錬法。1. A raw material consisting of a mixture of metal sulfide ore and a solvent is appropriately mixed with air and a fluid solid fuel, and this is continuously charged into a smelting furnace and melted to produce 〓 and 〓. A smelting process in which the smelting furnace from the furnace is solidified and crushed and continuously charged into the smelting furnace to absorb most of the target metal contained in the smelting furnace into the smelting furnace. A separation step in which the entire amount of the product of the smelting process is transferred to a separation tank and separated into a In a continuous smelting method for sulfide metal ore, which comprises a smelting process in which the raw material is charged into the smelting furnace to produce the target metal and the above-mentioned smelting furnace, the above-mentioned raw material charged to the smelting furnace in the smelting process is melted in advance. The minimum amount of air blowing to ensure the required stirring of the solution to promote acceleration is set according to the operating conditions, and the grade of metal sulfide ore charged to the smelting furnace and the amount produced in the smelting furnace are determined. In addition to the oxidizing air flow rate calculated to maintain the target grade based on the grade of and, the supplementary air amount necessary to maintain the minimum air flow rate and the fluid solid fuel corresponding to the grade of the metal sulfide ore. Blow directly into the solution through a lance, and effectively oxidize components to be oxidized such as iron and sulfur in the solution in the smelting furnace of the smelting process, and more rapidly transfer heat within the solution. The minimum amount of air blowing to ensure the required agitation of the solution is set according to the grade charged into the smelting furnace and the amount of oxygen in the air, and the components of 〓 from the separation tank are In addition to the oxidizing air flow rate calculated based on the composition and amount of the refrigerant, the replenishment air amount necessary to maintain the minimum air flow rate and the corresponding fluid solid fuel according to the grade are added to the lance. A method for continuous smelting of metal sulfide, characterized in that the metal sulfide is blown directly into the solution through the sulfide.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11226379A JPS5635734A (en) | 1979-09-01 | 1979-09-01 | Continuously refining method for sulfide metal ore |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11226379A JPS5635734A (en) | 1979-09-01 | 1979-09-01 | Continuously refining method for sulfide metal ore |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5635734A JPS5635734A (en) | 1981-04-08 |
| JPS628489B2 true JPS628489B2 (en) | 1987-02-23 |
Family
ID=14582318
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP11226379A Granted JPS5635734A (en) | 1979-09-01 | 1979-09-01 | Continuously refining method for sulfide metal ore |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5635734A (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3509603B2 (en) * | 1998-03-05 | 2004-03-22 | Jfeスチール株式会社 | Extra-thick H-section steel with excellent toughness and yield strength of 325 MPa or more |
| JP7459660B2 (en) * | 2020-05-27 | 2024-04-02 | 住友金属鉱山株式会社 | Oxidized ore smelting method |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5443441B2 (en) * | 1973-06-15 | 1979-12-20 |
-
1979
- 1979-09-01 JP JP11226379A patent/JPS5635734A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5635734A (en) | 1981-04-08 |
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