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JPH0435533B2 - - Google Patents
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JPH0435533B2 - - Google Patents

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Publication number
JPH0435533B2
JPH0435533B2 JP10570184A JP10570184A JPH0435533B2 JP H0435533 B2 JPH0435533 B2 JP H0435533B2 JP 10570184 A JP10570184 A JP 10570184A JP 10570184 A JP10570184 A JP 10570184A JP H0435533 B2 JPH0435533 B2 JP H0435533B2
Authority
JP
Japan
Prior art keywords
concentrate
burner
oxygen
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flame
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
JP10570184A
Other languages
Japanese (ja)
Other versions
JPS60248832A (en
Inventor
Yukio Shibata
Kenichi Moryama
Nobumasa Iemori
Harumasa Kurokawa
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.)
Sumitomo Metal Mining Co Ltd
Original Assignee
Sumitomo Metal Mining Co 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 Mining Co Ltd filed Critical Sumitomo Metal Mining Co Ltd
Priority to JP10570184A priority Critical patent/JPS60248832A/en
Publication of JPS60248832A publication Critical patent/JPS60248832A/en
Publication of JPH0435533B2 publication Critical patent/JPH0435533B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】[Detailed description of the invention]

〔産業上の利用分野〕 本発明は自溶製錬炉において反応用空気の一部
を高濃度の酸素で置換したときの高濃度酸素及び
反応用気体の吹込み方法並びに高濃度酸素を使用
するのに適した精鉱バーナーの構造に関するもの
である。 〔従来の技術〕 自溶炉においては乾燥した精鉱、例えば銅精鉱
を反応用空気又は酸素富化空気と共にリアクシヨ
ンシヤフトの上部に設けられた精鉱バーナーから
吹き込み、瞬間的に精鉱を酸化溶融し銅等の有価
金属を〓として濃縮する。この場合、精鉱と反応
用空気又は酸素富化空気とが均一に混合し、リア
クシヨンシヤフト中を落下する極めて短時間のう
ちに均一な酸化反応が進行するようにすることが
重要である。この混合状態が悪く局部的に未反
応、未溶解物が生成すると、これがリアクシヨン
シヤフト下部のセトラーに堆積して〓の生成を妨
げたり、〓温度、〓品位の大きな変動を生じた
り、ダストの炉外への飛散量が多くなつたりして
操炉上の困難を招くのみならず、反応が集中して
起る部分では局部的加熱が起り、リアクシヨンシ
ヤフトの煉瓦を損傷する結果となる。 このような均一な混合と反応状態を得るために
は、精鉱シユートから落下する精鉱に吹き込まれ
る反応用気体の流速を80m/sec以上に保つ必要
がある。即ち、精鉱と送風中の酸素との反応効率
を高め、反応時間を短縮するためには精鉱シユー
ト出口部の精鉱バーナーコーン内に安定した火炎
を形成させると共に火炎内に精鉱を集中し、且つ
均一に分散させ、更に火炎内への酸素の供給速度
を速くして酸素の供給を短時間で行なうことが必
要である。 若し精鉱シユート出口部に安定した火炎が形成
されないと、精鉱と酸素の反応終了に要する時間
が長くなるため、炉の設計上シヤフト部での滞留
時間を稼ぐためシヤフト高さを高くする必要があ
り、このことは放散熱の増大につながる。しかし
例え火炎が形成されても火炎内への精鉱の集中度
が悪いと火炎外へ分散した精鉱はシヤフト部では
殆んど燃焼せず、ダストとして廃熱ボイラーへ飛
散し、ダストトラブルの原因となる。一方火炎内
での精鉱分散が均一でないと、精鉱が過度に集中
した部分の火炎温度が下がると共に、その部分に
必要な酸素の供給が追いつかず、ますますその部
分の温度が下がり、一部の精鉱はシヤフト部では
完全に溶融せず、セトラー部に落下して未燃、未
溶融の堆積物となり、一部粒径の小さい精鉱はダ
ストとなり廃熱ボイラーへ飛散し、自溶炉の〓板
取作業や廃熱ボイラーの操業に支障をもたらすこ
とになる。 更に、安定した火炎が形成され、火炎内への精
鉱の集中及び均一分散が良くても火炎内への酸素
の供給が不充分な場合は、火炎内での精鉱の燃焼
が充分でなくなり、未燃物が残る現象をおこす。 従来の自溶炉の精鉱バーナーはこの点で満足の
行くものではない。即ち、第3図は従来の精鉱バ
ーナーを示す断面図で、精鉱バーナー本体1の下
部はベンチユリー状絞り部2を有し、その下方は
すそ拡がりになつたバーナーコーン3が形成され
ている。精鉱バーナー本体1内の中央に管状の精
鉱シユート4を、その先端をベンチユリー状絞り
部2よりやゝ下方に突出するように垂設し、更に
精鉱シユート4の中心を貫通して燃料バーナー5
がバーナーコーン3の出口部付近にその先端を開
口している。燃料バーナー5の精鉱シユート4の
出口より下方のバーナーコーン3の部分には、落
下する精鉱を分散する分散コーン6が設けられて
いる。送風管7を通つて供給される反応用空気が
精鉱シユート4の周囲のベンチユリー状絞り部2
から、精鉱シユート4を通つて落下する精鉱に吹
き込まれるように構成されている。 しかし送風中の酸素濃度が比較的低く(21〜
40vol%)、且つ送風温度が500℃程度である場合
には、着火源となる燃料バーナー5の先端がバー
ナーコーン3出口部近くに位置していることと相
俟つてバーナーコーン3内では精鉱粒子をその着
火温度まで加熱できない為精鉱シユート4出口部
に火炎を形成することは不可能であつた。 近時精鉱処理量の増加やエネルギーコストの低
下の為に酸素富化空気を使用するようになつてき
たが、この操業において、精鉱バーナーとして従
来の第3図に示すバーナーを用いると送風管7か
ら酸素富化空気が送られるので、そのときの精鉱
装入量と酸素富化割合によつては窒素の体積減少
分だけベンチユリー状絞り部2を流れる反応用気
体の流速が所望値である80m/secを下まわり、
精鉱と反応用気体との均一な混合ができなくなる
場合が生ずる。この問題を解決するために発明者
等は実願昭58−124820号を出願した。この考案は
従来の精鉱バーナーのベンチユリー状絞り部2の
反応気体の流速を調節できるように精鉱シユート
4下端付近の外周に位置変更可能な流速調節コー
ンを設けたものである。しかしながら、この装置
では前述の理由によつて精鉱シユート4出口部で
は火炎を形成することはできなかつた。 一方酸素富化用の純度の高い酸素を精鉱シユー
ト4内に直接導入する方法も考えられる。この場
合高濃度酸素の一部が優先的に補助燃料である重
油の燃焼に利用されるため、重油の火炎温度は通
常の空気を用いた場合より非常に高くなる他、精
鉱と高濃度酸素が予め混合されている為着火エネ
ルギーは少なくて済み、バーナーコーン3内に火
炎を生ずることができる。しかし火炎は安定せ
ず、精鉱シユート4を離れた精鉱がバーナーコー
ン3内に拡がる為、バーナーコーン3内側に精鉱
の半溶融物が付着し、操業を安定的に連続するこ
とが困難となり、また高濃度酸素を精鉱シユート
4内に供給するためベンチユリー状絞り部2で精
鉱シユート4周囲から供給する反応用気体の流速
が低下し、火炎内への酸素の供給が精鉱の燃焼速
度に追いつかず、シヤフト部まで燃焼状態を維持
することができず、セトラー部への未燃、未溶融
物の堆積が認められた。 〔発明が解決しようとする問題点〕 本発明は前述の問題点を解決し、精鉱シユート
先端に安定した火炎を形成し、該火炎内へ精鉱を
集中し、且つ均一に分布するように供給すると共
に、火炎内への酸素の供給速度が精鉱の燃焼反応
を妨げないようにして、精鉱と酸素との反応効率
を上げ、反応終了時間を短縮する自溶製錬炉の操
業方法及びそのための精鉱バーナーを提供するこ
とを目的とするものである。 〔問題点を解決するための手段〕 この目的を達成するために、本発明はその操業
方法並びに精鉱バーナーの構造を特許請求の範囲
に記載したように構成したものである。 本発明の精鉱バーナーの構造をその一実施例に
ついて説明すると第1図において、精鉱バーナー
本体1内の中央に設けられた管状の精鉱シユート
4の内側に燃料バーナー5を取り囲んで酸素吹込
管8を設け、酸素吹込管8出口部は中央部に開口
面積調整スペーサー9を設けて開口面積をせば
め、開口部は酸素吹込管8の軸方向に対し適当な
角度を持つた案内羽根10を設けてある。第2図
は酸素吹込管8出口部の断面図であつて、酸素吹
出口の吹出し速度は30m/sec以上80m/sec以下
とするのが好ましく、案内羽根10の酸素吹込管
8の軸方向に対する傾斜角は20〜70°、案内羽根
10の枚数は5〜15枚が適当である。流速調節コ
ーン11は精鉱バーナー本体1の上面を貫通する
複数の吊りロツド12に固着されて、精鉱バーナ
ー本体1の上面からベンチユリー状絞り部2の近
傍に吊り下げられており、止め金具13によつて
その固定位置を変えることによつて、吊りロツド
12の精鉱バーナー本体1の内部に延長する長さ
を変え、流速調節コーン11の位置を精鉱シユー
ト4の外面に沿つて上下にずらすことができるよ
うになつている。流速調節コーン11は下側を上
拡がりの截頭円錐状に形成し、そのテーパー角度
βは精鉱バーナー本体1内面のテーパー角度γと
等しいか、あるいはそれよりやゝ小さい角度とす
るのが好ましい。また止め金具13はナツトを用
い、吊りロツド12にネジを設けてこれにねじ込
む方法でも良いし、吊りロツド12に多数の小孔
を設け適当な位置の小孔にピンをさし込む方法で
も良い。 〔作用〕 本発明の精鉱バーナーの構成は上記のようであ
つて、この精鉱バーナーを用いて自溶炉を操業す
るに際しては、使用する高濃度酸素の一部若しく
は全部を精鉱バーナー本体1の酸素吹込管8から
供給すれば酸素はその先端に設けた案内羽根10
により旋回流として且つ高速で精鉱シユート内に
供給され、精鉱と高濃度酸素との混合が均一且つ
充分に行なわれるので着火エネルギーは少なくて
すみ、精鉱シユート4を離れた精鉱がバーナーコ
ーン3内で直ちに火炎を形成することができる。
また高濃度酸素の一部又は全部が精鉱シユート4
内の酸素吹込管8から供給されるので、送風管7
から供給する空気又は酸素富化空気量は酸素含有
気体として空気のみを使用しているときに比して
少なくて済み、精鉱シユート4の周囲のベンチユ
リー部2に供給する反応用気体の流速が80m/
sec以下となるようなときには精鉱シユート4外
周における流速調整コーン11の位置を調節して
送風管7からベンチユリー状絞り部2へ吹込む間
隙を狭くし、反応用気体の流速を80〜240m/sec
になるようにすればバーナーコーン3内に生成し
た火炎内への酸素の供給が十分に行なわれて精鉱
と酸素の反応が極めて短時間で終了するようにな
り、本発明の自溶製錬炉の操業方法の目的を達成
することができる。 精鉱シユート4周囲のベンチユリー状絞り部2
に供給する反応用気体の流速を80〜240m/secに
保つ理由については80m/sec以下になつた場合
については前にも述べたが、240m/sec以上とな
るとこの部分の気体の流通抵抗が増して送風機の
消費電力が増すほか、集中的に供給された精鉱が
火炎外へ分散し、未燃焼精鉱として廃熱ボイラー
の方へ飛散するものが増加する傾向を示すので好
ましくない。 また供給される高濃度酸素は一般的には精鉱シ
ユート4に供給されるが、高濃度酸素の使用量が
増加して全量を精鉱シユート4に供給すると圧損
が大となり過ぎるようなとき、シヤフト部のフオ
ーカスが上昇してシヤフト部炉壁の付着物が部分
的に薄くなり、フオーカスの位置を変動させたい
時などには高濃度酸素の一部を反応用空気と混合
する必要がある。 〔実施例〕 以下実施例について説明する。 実施例 1 第1図に示す本発明に従つた精鉱バーナー4本
を備えた自溶炉で、その精鉱バーナーの案内羽根
10の枚数10枚、羽根の取付角度45°のものを用
い、銅精鉱の処理量は55t/H、酸素純度90%の
酸素富化用の酸素5700m3/Hを精鉱シユート4か
ら3200m3/H、送風空気に混入して2500m3/H使
用して操業した。このとき酸素を富化した送風の
ベンチユリー状絞り部2の流速は92m/Sで、80
m/Sを超えていたので、特に流速調整コーン1
1を用いてベンチユリー状絞り部の流速を早める
ような操作は必要としなかつた。この操業におい
てはバーナーコーン3において、火炎が形成され
ており、セトラー部においても未燃鉱石の堆積は
認められなかつた。結果を第1表に示す。 実施例 2〜4 実施例1と同じ精鉱バーナーを使用し、銅精鉱
の処理量は夫々40、50、60t/H、富化用の酸素
の使用量4600〜6000m3/Hを精鉱シユート4より
3200〜3000m3/H吹込み、残りは送風中に混入し
て使用した。実施例2ではベンチユリー状絞り部
2の送風の流速が流速調整コーン11を用いない
と80m/S以下となるので、流速調整コーンを使
用してベンチユリー状絞り部2の流速を150m/
Sとし、また実施例3、4では、更にこの部分の
流速を早くして210m/Sとなるように調節して
操業した結果、いずれもバーナーコーン3におい
て火炎の形成があり、セトラー部における未燃鉱
石の堆積は認められなかつた。 実施例 5 実施例1と同じ精鉱バーナーを使用し、銅精鉱
の処理量は35t/H、富化酸素の使用量3600m3
Hの全量を精鉱シユート4より吹込み、ベンチユ
リー状絞り部の送風の流速は流速調整コーン11
を使用して120m/Sに調節して操業した。その
結果、バーナーコーン3において火炎の形成があ
り、セトラー部における未燃鉱石の堆積は認めら
れなかつた。 比較例 1 第3図に示す従来の精鉱バーナー4本を備えた
自溶炉で、銅精鉱55t/H、酸素純度90%の酸素
富化用の酸素5500m3/Hを送風空気に混入して操
業した。このとき酸素を富化した送風のベンチユ
リー状絞り部2の流速は105m/Sで、適正値と
思われる80m/Sを超えてはいたが、バーナーコ
ーン3において火炎形成は認められず、セトラー
部において未燃鉱石の堆積があつた。 比較例 2 実施例1と同じ本発明に従つた精鉱バーナー4
本を備えた自溶炉で銅精鉱40t/H、酸素純度90
%の酸素富化用の酸素4400m3/Hを、精鉱シユー
ト4から3200m3/H、送風空気に混入して1200
m3/Hを使用して操業した。このとき酸素を富化
した送風のベンチユリー状絞り部2の流速は、流
速調整コーン11を使用せず、成り行きにまかせ
たところ、67m/Sで本発明の操業方法の範囲外
であつた。このときバーナーコーン3において火
炎は形成されていたが、セトラー部において未燃
鉱石の堆積があつた。 前記実施例2〜5、並びに比較例1、2の結果
を第1表に併記した。
[Industrial Application Field] The present invention relates to a method for blowing high concentration oxygen and reaction gas when a part of the reaction air is replaced with high concentration oxygen in a flash smelting furnace, and a method for using high concentration oxygen. The present invention relates to the structure of a concentrate burner suitable for [Prior art] In a flash-smelting furnace, dry concentrate, such as copper concentrate, is blown together with reaction air or oxygen-enriched air from a concentrate burner installed at the top of a reaction shaft, and the concentrate is instantaneously blown into the furnace. Melts with oxidation and concentrates valuable metals such as copper. In this case, it is important that the concentrate and the reaction air or oxygen-enriched air are uniformly mixed so that a uniform oxidation reaction proceeds within a very short period of time as they fall through the reaction shaft. If this mixing condition is poor and unreacted or undissolved substances are generated locally, they may accumulate in the settler at the bottom of the reaction shaft and prevent the production of 〓, cause large fluctuations in 〓 temperature and quality, or cause dust. This not only causes difficulties in operating the reactor due to the increased amount of scattering outside the reactor, but also causes local heating in areas where reactions occur in a concentrated manner, resulting in damage to the bricks of the reaction shaft. In order to obtain such uniform mixing and reaction conditions, it is necessary to maintain the flow rate of the reaction gas blown into the concentrate falling from the concentrate chute at 80 m/sec or more. In other words, in order to increase the efficiency of the reaction between the concentrate and the oxygen being blown and shorten the reaction time, it is necessary to form a stable flame in the concentrate burner cone at the outlet of the concentrate chute and concentrate the concentrate in the flame. It is necessary to disperse the oxygen uniformly and to increase the rate of oxygen supply into the flame so that the oxygen can be supplied in a short time. If a stable flame is not formed at the exit of the concentrate chute, the time required for the reaction between the concentrate and oxygen to complete will be longer, so the height of the shaft should be increased in order to increase the residence time in the shaft part due to the furnace design. This leads to increased heat dissipation. However, even if a flame is formed, if the concentration of concentrate in the flame is poor, the concentrate dispersed outside the flame will hardly be combusted in the shaft section and will be scattered as dust to the waste heat boiler, causing dust troubles. Cause. On the other hand, if the concentrate dispersion in the flame is not uniform, the flame temperature will drop in areas where concentrate is excessively concentrated, and the supply of oxygen necessary for that area will not be able to keep up, causing the temperature in that area to drop even further. Some concentrates do not completely melt in the shaft section and fall into the settler section, becoming unburned and unmelted deposits, and some concentrates with small particle sizes become dust and scatter to the waste heat boiler, where they self-dissolve. This will cause trouble in the furnace boarding work and in the operation of the waste heat boiler. Furthermore, even if a stable flame is formed and the concentration and uniform distribution of the concentrate in the flame is good, if the supply of oxygen to the flame is insufficient, the concentrate will not burn sufficiently in the flame. , causing a phenomenon in which unburned materials remain. Conventional flash furnace concentrate burners are unsatisfactory in this respect. That is, FIG. 3 is a cross-sectional view showing a conventional concentrate burner, in which the lower part of the concentrate burner main body 1 has a ventilate-shaped constriction part 2, and below that, a burner cone 3 with a widened base is formed. . A tubular concentrate chute 4 is installed vertically in the center of the concentrate burner body 1 so that its tip protrudes slightly below the ventilate-shaped constriction part 2, and the fuel is passed through the center of the concentrate chute 4. burner 5
has its tip opened near the outlet of the burner cone 3. A dispersion cone 6 for dispersing falling concentrate is provided in a portion of the burner cone 3 below the outlet of the concentrate chute 4 of the fuel burner 5. The reaction air supplied through the blast pipe 7 passes through the ventilated constriction 2 around the concentrate chute 4.
It is configured to be blown into the concentrate falling through the concentrate chute 4 from the concentrate chute 4 . However, the oxygen concentration in the air is relatively low (21~
40vol%) and the air blowing temperature is about 500℃, the tip of the fuel burner 5, which is the ignition source, is located near the outlet of the burner cone 3, and the inside of the burner cone 3 is heated. It was impossible to form a flame at the outlet of the concentrate chute 4 because the ore particles could not be heated to their ignition temperature. Recently, oxygen-enriched air has been used to increase the throughput of concentrates and reduce energy costs. Since oxygen-enriched air is sent from the pipe 7, depending on the amount of concentrate charged and the oxygen enrichment ratio, the flow rate of the reaction gas flowing through the ventilate-shaped constriction part 2 will be adjusted to the desired value by the volume reduction of nitrogen. below 80m/sec,
Uniform mixing of the concentrate and the reaction gas may not be possible in some cases. In order to solve this problem, the inventors filed Utility Model Application No. 124820/1983. In this invention, a repositionable flow rate adjusting cone is provided on the outer periphery near the lower end of the concentrate chute 4 so as to adjust the flow rate of the reaction gas in the ventilated constriction section 2 of the conventional concentrate burner. However, with this device, it was not possible to form a flame at the outlet of the concentrate chute 4 for the reasons mentioned above. On the other hand, a method of directly introducing highly pure oxygen for oxygen enrichment into the concentrate chute 4 is also considered. In this case, a part of the high concentration oxygen is preferentially used for the combustion of heavy oil, which is the auxiliary fuel, so the flame temperature of the heavy oil becomes much higher than when normal air is used. Since these are pre-mixed, less ignition energy is required and a flame can be generated within the burner cone 3. However, the flame is not stable and the concentrate that has left the concentrate chute 4 spreads into the burner cone 3, so semi-molten concentrate adheres to the inside of the burner cone 3, making it difficult to continue stable operation. In addition, in order to supply high concentration oxygen into the concentrate chute 4, the flow rate of the reaction gas supplied from around the concentrate chute 4 in the ventilate-like constriction part 2 is reduced, and the supply of oxygen into the flame is reduced. It was not possible to keep up with the combustion speed and maintain the combustion state up to the shaft section, and unburnt and unmelted materials were observed to accumulate in the settler section. [Problems to be Solved by the Invention] The present invention solves the above-mentioned problems by forming a stable flame at the tip of the concentrate chute, concentrating the concentrate in the flame, and distributing it uniformly. A method for operating a flash smelting furnace that increases the efficiency of the reaction between concentrate and oxygen and shortens the reaction completion time by ensuring that the rate of oxygen supply into the flame does not impede the combustion reaction of the concentrate. and to provide a concentrate burner therefor. [Means for Solving the Problems] In order to achieve this object, the present invention comprises an operating method and a structure of a concentrate burner as described in the claims. To explain the structure of the concentrate burner of the present invention with reference to an embodiment thereof, as shown in FIG. A tube 8 is provided, and an opening area adjustment spacer 9 is provided in the center of the outlet of the oxygen blowing tube 8 to narrow the opening area, and a guide vane 10 is provided at the opening at an appropriate angle with respect to the axial direction of the oxygen blowing tube 8. It is provided. FIG. 2 is a sectional view of the outlet of the oxygen blowing pipe 8, and the blowing speed of the oxygen blowing port is preferably 30 m/sec or more and 80 m/sec or less, and the guide vane 10 is relative to the axial direction of the oxygen blowing pipe 8. The appropriate inclination angle is 20 to 70 degrees, and the number of guide vanes 10 is 5 to 15. The flow rate adjusting cone 11 is fixed to a plurality of hanging rods 12 passing through the upper surface of the concentrate burner main body 1, and is suspended from the upper surface of the concentrate burner main body 1 near the ventilate-shaped constriction portion 2. By changing its fixing position, the length of the hanging rod 12 extending into the concentrate burner body 1 can be changed, and the position of the flow rate adjusting cone 11 can be moved up or down along the outer surface of the concentrate chute 4. It is now possible to shift it. The flow rate adjusting cone 11 is formed in the shape of a truncated cone with its lower side expanding upward, and its taper angle β is preferably equal to or slightly smaller than the taper angle γ of the inner surface of the concentrate burner body 1. . Further, the stopper 13 may be a nut, and a screw may be provided on the hanging rod 12 and screwed into this, or a method may be used in which a number of small holes are provided in the hanging rod 12 and a pin is inserted into the small hole at an appropriate position. . [Function] The structure of the concentrate burner of the present invention is as described above, and when operating a flash furnace using this concentrate burner, part or all of the high concentration oxygen used is transferred to the concentrate burner body. If oxygen is supplied from the oxygen blowing pipe 8 of 1, the oxygen will flow through the guide vane 10 provided at its tip.
The concentrate is supplied into the concentrate chute as a swirling flow at high speed, and as the concentrate and high concentration oxygen are mixed uniformly and sufficiently, the ignition energy is small, and the concentrate leaving the concentrate chute 4 is fed into the burner. A flame can be formed immediately within the cone 3.
In addition, some or all of the high concentration oxygen is concentrated in the concentrate chute 4.
Since the oxygen is supplied from the oxygen blowing pipe 8 inside the air blowing pipe 7
The amount of air or oxygen-enriched air supplied from the concentrate chute 4 can be reduced compared to when only air is used as the oxygen-containing gas, and the flow rate of the reaction gas supplied to the ventilate section 2 around the concentrate chute 4 can be reduced. 80m/
sec or less, the position of the flow rate adjusting cone 11 on the outer periphery of the concentrate chute 4 is adjusted to narrow the gap through which the gas is blown from the blast pipe 7 to the ventilated constriction part 2, and the flow rate of the reaction gas is adjusted to 80 to 240 m/sec. sec
By doing so, oxygen is sufficiently supplied into the flame generated in the burner cone 3, and the reaction between the concentrate and oxygen is completed in a very short time, and the self-smelting method of the present invention The purpose of the furnace operating method can be achieved. Ventilation-shaped constriction section 2 around the concentrate chute 4
The reason for keeping the flow rate of the reaction gas supplied to the area between 80 and 240 m/sec is as mentioned above when the flow rate is 80 m/sec or less, but when it is over 240 m/sec, the flow resistance of the gas in this area increases. This is undesirable because not only does the power consumption of the blower increase, but also the concentratedly supplied concentrate is dispersed outside the flame, and the amount of unburned concentrate that is scattered toward the waste heat boiler increases. In addition, the supplied high concentration oxygen is generally supplied to the concentrate chute 4, but when the amount of high concentration oxygen used increases and the pressure drop becomes too large if the entire amount is supplied to the concentrate chute 4, When the focus of the shaft section rises and deposits on the furnace wall of the shaft section become partially thin, and it is desired to change the position of the focus, it is necessary to mix a portion of the high concentration oxygen with the reaction air. [Example] Examples will be described below. Example 1 A flash-smelting furnace equipped with four concentrate burners according to the present invention as shown in FIG. The processing amount of copper concentrate is 55t/H, 5700m 3 /H of oxygen enriched with 90% oxygen purity is used from concentrate chute 4 at 3200m 3 /H, and mixed with the blast air for 2500m 3 /H. It was operated. At this time, the flow velocity of the ventilated constriction section 2 of the oxygen-enriched air was 92 m/s, which was 80 m/s.
m/S, especially the flow rate adjustment cone 1.
Using No. 1, no operation was required to increase the flow velocity in the ventilate-like constriction section. In this operation, a flame was formed in the burner cone 3, and no unburned ore was observed to accumulate in the settler section. The results are shown in Table 1. Examples 2 to 4 Using the same concentrate burner as in Example 1, the processing amount of copper concentrate was 40, 50, and 60 t/H, respectively, and the amount of oxygen used for enrichment was 4600 to 6000 m 3 /H. From Shoot 4
3,200 to 3,000 m 3 /H was blown, and the rest was used by mixing it into the air blowing. In Example 2, the flow velocity of the ventilated constriction part 2 is 80 m/s or less without using the flow velocity adjustment cone 11, so the flow velocity of the ventilated constriction part 2 is adjusted to 150 m/s using the flow velocity regulation cone.
In addition, in Examples 3 and 4, the flow velocity in this part was further increased to 210 m/S, and as a result, in both cases, flame was formed in the burner cone 3, and the flow velocity in the settler part was increased. No accumulation of combustion ore was observed. Example 5 The same concentrate burner as in Example 1 was used, the processing amount of copper concentrate was 35 t/H, and the amount of enriched oxygen used was 3600 m 3 /
The entire amount of H is blown into the concentrate chute 4, and the flow rate of the air through the ventilated constriction part is adjusted by the flow rate adjustment cone 11.
It was operated at a speed of 120 m/s. As a result, flame was formed in the burner cone 3, and no accumulation of unburned ore was observed in the settler section. Comparative Example 1 In a flash smelting furnace equipped with four conventional concentrate burners as shown in Figure 3, 55 t/H of copper concentrate and 5500 m 3 /H of oxygen enriched with 90% oxygen purity were mixed into the blast air. It was operated. At this time, the flow velocity of oxygen-enriched air through the ventilated constriction section 2 was 105 m/s, which exceeded the appropriate value of 80 m/s, but no flame formation was observed in the burner cone 3, and no flame formation was observed in the settler section. There was a deposit of unburned ore. Comparative Example 2 Concentrate burner 4 according to the invention as in Example 1
Copper concentrate 40t/H, oxygen purity 90 in a flash furnace equipped with a book
4400 m 3 /H of oxygen for oxygen enrichment of 3200 m 3 /H from the concentrate chute 4 was mixed into the blast air and 1200 m 3 /H of oxygen was mixed into the blast air.
The operation was performed using m 3 /H. At this time, the flow velocity of the oxygen-enriched ventilated air constriction section 2 was 67 m/s, which was outside the range of the operating method of the present invention, when the flow velocity adjustment cone 11 was not used and the flow velocity was left as it was. At this time, a flame was formed in the burner cone 3, but unburnt ore was deposited in the settler section. The results of Examples 2 to 5 and Comparative Examples 1 and 2 are also listed in Table 1.

【表】【table】

〔発明の効果〕〔Effect of the invention〕

第1表の結果から明らかなように、本発明の精
鉱バーナーを使用し、本発明の方法に従つて操業
した実施例1〜5の場合には、いずれもバーナー
コーンに火炎が形成され、セトラー部に未燃鉱石
による堆積は認められず、本発明によつて精鉱シ
ユート内での酸素と精鉱の混合が十分うまく行つ
ていることがうかがわれ、本発明によらない精鉱
バーナーの使用、あるいは本発明の精鉱バーナー
は使用したが、本発明方法の範囲外の操業方法に
よる比較例1、2の場合のダスト発生率と比較し
てダスト発生が著しく低下していることも判る。 また比較例2に示すように精鉱バーナーのベン
チユリー状絞り部の流速が低下すると精鉱バーナ
ー先端のバーナーコーンに火炎形成はされるが、
酸素の供給が不充分なためバーナーコーン内の燃
焼状態をシヤフト部まで維持できず一部の精鉱が
未燃となりセトラー部への堆積が認められた。
As is clear from the results in Table 1, in Examples 1 to 5, which used the concentrate burner of the present invention and operated according to the method of the present invention, a flame was formed in the burner cone, No accumulation of unburned ore was observed in the settler section, indicating that oxygen and concentrate were mixed well in the concentrate chute according to the present invention. or the concentrate burner of the present invention was used, but the dust generation rate was significantly reduced compared to the dust generation rate in Comparative Examples 1 and 2 using an operating method outside the scope of the method of the present invention. I understand. Furthermore, as shown in Comparative Example 2, when the flow velocity of the ventilate-like constriction of the concentrate burner decreases, flame is formed in the burner cone at the tip of the concentrate burner, but
Due to insufficient supply of oxygen, the combustion state inside the burner cone could not be maintained up to the shaft section, and some concentrate was left unburned and deposited in the settler section.

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

第1図は本発明の自溶製錬炉用精鉱バーナーの
断面図、第2図は第1図の酸素吹込管8出口部の
断面図、第3図は従来の精鉱バーナーの断面図で
ある。 1……精鉱バーナー本体、2……ベンチユリー
状絞り部、3……バーナーコーン、4……精鉱シ
ユート、5……燃料バーナー、6……分散コー
ン、7……送風管、8……酸素吹込管、9……開
口面積調整スペーサー、10……案内羽根、11
……流速調整コーン、12……吊りロツド、13
……止め金具。
Fig. 1 is a sectional view of the concentrate burner for flash smelting furnace of the present invention, Fig. 2 is a sectional view of the outlet of the oxygen blowing pipe 8 of Fig. 1, and Fig. 3 is a sectional view of a conventional concentrate burner. It is. DESCRIPTION OF SYMBOLS 1... Concentrate burner main body, 2... Ventilate-shaped constriction part, 3... Burner cone, 4... Concentrate chute, 5... Fuel burner, 6... Dispersion cone, 7... Blow pipe, 8... Oxygen blowing pipe, 9... Opening area adjustment spacer, 10... Guide vane, 11
...Flow rate adjustment cone, 12...Hanging rod, 13
……Fasteners.

Claims (1)

【特許請求の範囲】 1 反応用空気の一部を高濃度酸素で置換する自
溶製錬炉の操業方法において、使用する高濃度酸
素の一部若しくは全部を精鉱バーナーの精鉱シユ
ート内に旋回流として吹込み、且つ精鉱シユート
出口周囲のベンチユリー部に供給する反応用気体
の流速を80〜240m/secとすることを特徴とする
自溶製錬炉の操業方法。 2 バーナー本体内中央に位置し、バーナー本体
のベンチユリー状絞り部に延長して設けられた管
状の精鉱シユートを有し、該精鉱シユートとベン
チユリー状絞り部との間から反応用気体を精鉱と
共にリアクシヨンシヤフトの上部に吹き込む自溶
製錬炉用精鉱バーナーにおいて、精鉱シユート内
に燃料バーナーをとりかこんで酸素吹込管を設
け、精鉱シユート内におけるその先端開口部に吹
込酸素に旋回流を生ぜしめるよう案内羽根を設
け、且つ精鉱シユート外周に接しベンチユリー部
近傍に精鉱シユートの長手方向に沿い位置変更可
能に流速調節コーンを設けたことを特徴とする自
溶製錬炉用精鉱バーナー。
[Claims] 1. In a method of operating a flash smelting furnace in which a part of the reaction air is replaced with high concentration oxygen, part or all of the high concentration oxygen used is replaced in the concentrate chute of a concentrate burner. A method for operating a flash smelting furnace, characterized in that the flow rate of reaction gas is blown in as a swirling flow and supplied to a ventilate section around the outlet of a concentrate chute at a flow rate of 80 to 240 m/sec. 2 A tubular concentrate chute is located in the center of the burner body and extends to the ventilate-shaped constriction of the burner body, and the reaction gas is concentrated between the concentrate chute and the ventilate-shaped constriction. In a concentrate burner for a flash smelting furnace where ore is injected into the upper part of a reaction shaft, an oxygen blowing pipe is provided surrounding the fuel burner in the concentrate chute, and the oxygen blowing pipe is installed in the tip opening in the concentrate chute. A flash smelting furnace characterized in that a guide vane is provided to generate a swirling flow, and a flow rate adjusting cone is provided in contact with the outer periphery of the concentrate chute and near the ventilate part so as to be able to change its position along the longitudinal direction of the concentrate chute. Concentrate burner for use.
JP10570184A 1984-05-25 1984-05-25 Operating method of flash smelting furnace and concentrate burner for flash smelting furnace Granted JPS60248832A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10570184A JPS60248832A (en) 1984-05-25 1984-05-25 Operating method of flash smelting furnace and concentrate burner for flash smelting furnace

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10570184A JPS60248832A (en) 1984-05-25 1984-05-25 Operating method of flash smelting furnace and concentrate burner for flash smelting furnace

Publications (2)

Publication Number Publication Date
JPS60248832A JPS60248832A (en) 1985-12-09
JPH0435533B2 true JPH0435533B2 (en) 1992-06-11

Family

ID=14414666

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10570184A Granted JPS60248832A (en) 1984-05-25 1984-05-25 Operating method of flash smelting furnace and concentrate burner for flash smelting furnace

Country Status (1)

Country Link
JP (1) JPS60248832A (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0339483Y2 (en) * 1988-03-23 1991-08-20
JP2723572B2 (en) * 1988-12-02 1998-03-09 住友金属鉱山株式会社 Flash smelting furnace
JP5208898B2 (en) * 2009-09-30 2013-06-12 パンパシフィック・カッパー株式会社 Operation method and raw material supply device of flash smelting furnace
FI121852B (en) * 2009-10-19 2011-05-13 Outotec Oyj Process for feeding fuel gas into the reaction shaft in a suspension melting furnace and burner
JP5561234B2 (en) * 2011-04-15 2014-07-30 住友金属鉱山株式会社 Concentrate burner and smelting furnace
US8889059B2 (en) * 2011-05-06 2014-11-18 Hatch Ltd. Slit lance burner for flash smelter
CN102268558B (en) * 2011-07-25 2012-11-28 阳谷祥光铜业有限公司 Floating entrainment metallurgical process and reactor thereof
CN106521182B (en) 2016-11-02 2019-05-21 阳谷祥光铜业有限公司 It is a kind of to revolve floating Copper making method and revolve floating Copper making device
JP6800796B2 (en) * 2017-03-31 2020-12-16 パンパシフィック・カッパー株式会社 Raw material supply equipment, flash smelting furnace, nozzle members
WO2021106884A1 (en) * 2019-11-25 2021-06-03 パンパシフィック・カッパー株式会社 Concentrate burner, flash furnace, and method for introducing reaction gas
CN115232980B (en) * 2022-08-22 2023-08-15 山东兴达化工有限公司 Filter residue recycling device for sulfuric acid production

Also Published As

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