JPH0224898B2 - - Google Patents
Info
- Publication number
- JPH0224898B2 JPH0224898B2 JP15947882A JP15947882A JPH0224898B2 JP H0224898 B2 JPH0224898 B2 JP H0224898B2 JP 15947882 A JP15947882 A JP 15947882A JP 15947882 A JP15947882 A JP 15947882A JP H0224898 B2 JPH0224898 B2 JP H0224898B2
- Authority
- JP
- Japan
- Prior art keywords
- coke
- flash
- furnace
- copper concentrate
- copper
- 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
Links
- 239000003245 coal Substances 0.000 claims description 37
- 239000000571 coke Substances 0.000 claims description 33
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 28
- 229910052802 copper Inorganic materials 0.000 claims description 28
- 239000010949 copper Substances 0.000 claims description 28
- 239000000446 fuel Substances 0.000 claims description 28
- 239000012141 concentrate Substances 0.000 claims description 23
- 239000007787 solid Substances 0.000 claims description 20
- 238000002844 melting Methods 0.000 claims description 17
- 238000003723 Smelting Methods 0.000 claims description 16
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 12
- 230000004907 flux Effects 0.000 claims description 11
- 238000000034 method Methods 0.000 claims description 10
- 239000002480 mineral oil Substances 0.000 claims description 9
- 235000010446 mineral oil Nutrition 0.000 claims description 9
- 239000000843 powder Substances 0.000 claims description 9
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 5
- 229910052760 oxygen Inorganic materials 0.000 claims description 5
- 239000001301 oxygen Substances 0.000 claims description 5
- 238000011144 upstream manufacturing Methods 0.000 claims description 4
- 239000003077 lignite Substances 0.000 claims description 3
- 239000000463 material Substances 0.000 claims description 2
- 230000008018 melting Effects 0.000 description 11
- 238000006243 chemical reaction Methods 0.000 description 9
- 239000000295 fuel oil Substances 0.000 description 9
- 238000002485 combustion reaction Methods 0.000 description 7
- 238000002156 mixing Methods 0.000 description 6
- 238000007254 oxidation reaction Methods 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- 238000010298 pulverizing process Methods 0.000 description 5
- 239000002994 raw material Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- 238000007667 floating Methods 0.000 description 4
- 239000007789 gas Substances 0.000 description 4
- 239000002893 slag Substances 0.000 description 4
- 239000010419 fine particle Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 230000001603 reducing effect Effects 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 2
- 238000007664 blowing Methods 0.000 description 2
- OMZSGWSJDCOLKM-UHFFFAOYSA-N copper(II) sulfide Chemical compound [S-2].[Cu+2] OMZSGWSJDCOLKM-UHFFFAOYSA-N 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 229910000640 Fe alloy Inorganic materials 0.000 description 1
- 229910001021 Ferroalloy Inorganic materials 0.000 description 1
- MBMLMWLHJBBADN-UHFFFAOYSA-N Ferrous sulfide Chemical compound [Fe]=S MBMLMWLHJBBADN-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 1
- 238000011017 operating method Methods 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000001172 regenerating effect Effects 0.000 description 1
- 238000010079 rubber tapping Methods 0.000 description 1
- 238000009628 steelmaking Methods 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 239000002918 waste heat Substances 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Landscapes
- Manufacture And Refinement Of Metals (AREA)
Description
発明の分野
本発明は、銅精鉱を熔錬する銅製錬自熔炉の燃
料を従来の鉱油から固体炭素質燃料に転換する技
術に関するものである。本発明は、特に微粉炭を
使用することなく鉱油の100%代替を図ることを
特徴とする。
発明の背景
銅製錬用自熔炉は、硫化銅精鉱(以下銅精鉱と
いう)をフラツクス等と共に装入し、同時に空気
或いは酸素富化空気を吹込み、酸化に際して発生
する反応熱を大半の熱源として銅精鉱の熔解及び
酸化製錬を行い、硫化銅及び硫化鉄を主体とする
熔体である〓(マツト)と酸化鉄の珪酸塩を主体
とした熔体である〓(スラグ)を産出する炉であ
る。この際、反応に伴つて発生する亜硫酸ガスを
含有する排ガスは濃硫酸製造の原料とされる。自
熔炉は精鉱の酸化反応熱を利用するため他の型式
の炉に比し、燃料消費率が低く、環境管理も好適
に行いうる点で我国では広く採用されている。
上記のように、自熔炉は原料の酸化反応熱を大
半の熱源としているが、不足熱量を補うために旧
来重油を燃焼していた。しかしながら、近年重油
価格高騰に伴い、微粉炭等の代替燃料を使用する
燃料転換策が積極的におし進められている。
しかしながら、銅製錬自熔炉に関しては実質的
に重油の全量を代替することがいまだ実施されて
おらず代替率は不満足な数値に止まり、また附帯
設備及びコストをかなり必要とし、これでは重油
代替の意義が少ない。
従来技術とその問題点
従来、自熔炉の鉱油燃焼の代替用としては専ら
微粉炭が考慮されたい。これは、通常の自熔炉に
おいてシヤフト内を降下する間に燃焼を終了する
には微粉炭のような極微粒(−200メツシユが80
〜90%)のものでないと使用できないと考えられ
たからである。また、通常の自熔炉温度において
は、原料中にS等の可燃性成分の少ないものでは
全量代替できないと考えられ、そのためコークス
粉の使用可能性は考慮だにされなかつた。そのた
め、代替燃料の有力候補としては微粉炭が専ら考
慮された。しかし、微粉炭の使用は次のような不
満足な点が多い:
(1) 微粉炭を使用する場合石炭を乾燥粉砕して微
粉炭を製造するので、そのための粉砕設備を必
要とし、粉砕コストも多大のものとなる。
(2) 微粉炭の製造及び輸送を含めての取扱いの際
に爆発防止の為の安全上の特別の配慮を要す
る。
(3) 微粉炭を使用すると、超微粉のため気流に乗
つて炉出口側に飛散し、シヤフト部で完全に燃
焼せず、炉出口側の廃熱回収部で燃焼する欠点
が生じる。
(4) 粉砕に伴う作業環境悪化の幣害が大きい。
(5) 微粉炭の安定した気流輸送が困難である。
発明の目的
本発明は、微粉炭のような極微粒寸にまで粉砕
されていない固体炭素質燃料によつてでも鉱油の
100%代替を可能とする自熔炉の操業方法の確立
を目的とする。
発明の概要
本発明者は、全く予想外に、空気或いは酸素富
化空気を650℃以上に予熱して吹込む高温熱風操
業の自熔炉においては、微粉炭のような微細なも
のでなくもつと粗い固体炭素質燃料を使用してで
も100%鉱油代替が実現しうることを見出した。
銅製錬用自熔炉において重油から固体炭素質燃料
の100%燃料転換を実現したのは、本発明者の知
る限り、先例がない。
斯くして、本発明は、銅精鉱、フラツクスその
他の装入物を装入し、同時に空気あるいは酸素富
化空気を650℃以上に予熱して吹込み、そして補
助燃料として固体炭素質燃料(但し微粉炭を除
く)のみを使用し、100%鉱油を代替したことを
特徴とする銅製錬自熔炉の操業方法を提供する。
ここで、固体炭素質燃料とは、微粉炭以外の各
種の等級の石炭、木炭およびコークスを包含す
る。本発明において使用するに好ましい固体炭素
質燃料は粉粒コークスおよび/あるいはサイズ40
mm以下の塊粒粉低質石炭である。微粉炭水準への
微粉化は不要である。
粉粒コークスとは、粉コークス、粒コークスあ
るいは両者の混合物を意味し、通常製鉄用に使用
されるような整粒された塊コークス以外の各種コ
ークスを包含するが、特にコークス炉からコーク
スを取出す際の冷却工程で副産する粉粒まじりコ
ークスである沈殿粉コークスの使用が望ましい。
沈殿粉コークスの粒度分布、成分および発熱量を
第1表に示す。又、沈殿粉コークス生成のフロー
シートを第1図に示す。
粉粒コークスとしては、上記沈殿粉コークス以
外に、ほぼ10mmアンダーの篩下コークスを単独あ
るいは混合して用いることができる。
塊粒粉低質石炭とは、微粉炭及び整粒された高
級石炭以外の石炭類を意味し、特に褐炭を実例と
する。本発明において用いられた褐炭であるワン
ボー炭(豪州産)について粒度分布、成分および
発熱量を第1表に示す。
FIELD OF THE INVENTION The present invention relates to a technology for converting the fuel for a copper smelting flash furnace for smelting copper concentrate from conventional mineral oil to solid carbonaceous fuel. The present invention is characterized in that it aims to replace mineral oil 100% without particularly using pulverized coal. Background of the Invention In a flash furnace for copper smelting, copper sulfide concentrate (hereinafter referred to as copper concentrate) is charged together with flux, etc., and air or oxygen-enriched air is blown in at the same time, and the reaction heat generated during oxidation is used as the majority of the heat source. Copper concentrate is melted and smelted by oxidation to produce 〓 (matsuto), which is a molten substance mainly composed of copper sulfide and iron sulfide, and 〓 (slag), which is a molten substance mainly composed of silicate of iron oxide. It is a furnace. At this time, the exhaust gas containing sulfur dioxide gas generated during the reaction is used as a raw material for producing concentrated sulfuric acid. Flash melting furnaces are widely used in Japan because they utilize the heat of the oxidation reaction of concentrates, resulting in lower fuel consumption and better environmental management than other types of furnaces. As mentioned above, flash melting furnaces use the heat of the oxidation reaction of the raw materials as their heat source, but in the past, heavy oil was burned to make up for the lack of heat. However, with the recent rise in heavy oil prices, fuel conversion measures using alternative fuels such as pulverized coal are being actively promoted. However, in copper smelting flash furnaces, substantially all of the heavy oil has not yet been replaced, and the replacement rate remains at an unsatisfactory value.In addition, considerable ancillary equipment and costs are required, which makes it difficult to replace heavy oil. Less is. Prior Art and Its Problems Conventionally, pulverized coal has been considered exclusively as a substitute for mineral oil combustion in flash-smelting furnaces. This is because extremely fine particles such as pulverized coal (-200 mesh are 80
This is because it was thought that it could only be used if it was (~90%). Furthermore, at normal flash-melting furnace temperatures, it is thought that it is not possible to completely replace raw materials with low combustible components such as S, so the possibility of using coke powder was not considered. Therefore, pulverized coal was considered as a potential alternative fuel. However, the use of pulverized coal has many unsatisfactory points as follows: (1) When using pulverized coal, pulverized coal is produced by drying and pulverizing coal, which requires pulverizing equipment and increases the cost of pulverizing. It becomes a huge thing. (2) Special safety considerations are required to prevent explosions during the production and handling of pulverized coal, including transportation. (3) When pulverized coal is used, it has the drawback that it is an ultra-fine powder that is carried by air currents and scattered toward the furnace exit, and is not completely combusted in the shaft section, but instead is combusted in the waste heat recovery section at the furnace exit. (4) The damage caused by the deterioration of the working environment due to crushing is significant. (5) Stable airflow transport of pulverized coal is difficult. OBJECT OF THE INVENTION The present invention provides a method for removing mineral oil even by solid carbonaceous fuel that has not been crushed to extremely fine particle size, such as pulverized coal.
The aim is to establish an operating method for flash-melting furnaces that enables 100% replacement. SUMMARY OF THE INVENTION The inventor of the present invention has completely unexpectedly discovered that in a high-temperature hot-air flash furnace in which air or oxygen-enriched air is preheated to 650°C or higher and is blown into the flask, fine particles such as pulverized coal are It was discovered that 100% mineral oil replacement can be achieved even by using coarse solid carbonaceous fuel.
As far as the inventors are aware, there is no precedent for achieving 100% fuel conversion from heavy oil to solid carbonaceous fuel in a copper smelting flash furnace. Thus, the present invention involves charging copper concentrate, flux, and other charges, simultaneously blowing air or oxygen-enriched air preheated to above 650°C, and using solid carbonaceous fuel (as an auxiliary fuel). Provided is a method for operating a copper smelting flash-smelting furnace characterized by using only pulverized coal (excluding pulverized coal) and replacing 100% mineral oil. Here, the solid carbonaceous fuel includes various grades of coal other than pulverized coal, charcoal, and coke. The preferred solid carbonaceous fuel for use in the present invention is granular coke and/or size 40
It is lump grain powder and low quality coal of less than mm. Pulverization to pulverized coal level is not necessary. Powder coke refers to powder coke, granular coke, or a mixture of the two, and includes various types of coke other than the sized lump coke normally used for steelmaking, but especially when coke is extracted from a coke oven. It is desirable to use precipitated coke powder, which is coke mixed with powder particles that is a by-product during the cooling process.
Table 1 shows the particle size distribution, components and calorific value of the precipitated coke powder. A flow sheet for producing precipitated coke is shown in FIG. As the powder coke, in addition to the above-mentioned precipitated coke powder, undersieve coke of approximately 10 mm under size can be used alone or in combination. Lump powder low-quality coal refers to coals other than pulverized coal and sized high-grade coal, and particularly lignite is taken as an example. Table 1 shows the particle size distribution, components, and calorific value of Wanbo coal (produced in Australia), which is the lignite used in the present invention.
【表】【table】
【表】
発明の具体的説明
本発明の好ましい態様について、以下に説明す
る。
第2図は、銅精鉱及び固体炭素質燃料を一緒に
自熔炉に装入するまでのフローを示す。調合ホツ
パ群1として、銅精鉱ホツパ2、固体炭素質燃料
の代表としての粉粒コークス用ホツパ3、及びフ
ラツクスホツパ4が並置され、それぞれ適当な源
から搬入される。例えば粉粒コークスは粉粒コー
クス鉱舎5からバケツトクレーン等によりホツパ
3内に搬入される。各ホツパの下側には、コンス
タントフイードコンベアのような切出装置6が設
けられており、各ホツパから所定量づつの原料切
出を行う。切出された原料成分は搬上コンベア8
によつて受入ビン10に送入される。搬上コンベ
アの代りにシユート、振動コンベア等の搬送設備
が使用されうる。受入ビンから装入原料はドライ
ヤーキルン12に投入されそしてケージミル14
により導管15を通して気流輸送される。気流輸
送より上流の段階で固体炭素質燃料と銅精鉱等と
を混合することにより、非常に均一に混合された
装入原料混合物が生成される。気流輸送された混
合物は、チヤンバ16及びサイクロン群18を経
てヘツドビン20に供給される。ヘツドビン20
の底から例えばビユーラーコンベアによつて装入
物は自熔炉精鉱バーナー22を通して装入され
る。サイクロンからドライヤーコツトレルを経て
の捕集ダストも装入される。自熔炉30は、シヤ
フト31、セツトラー32及びアツプテーク33
を具備する周知の構造のもので、熱風吹送手段
(図示なし)をも装備している。こうして、自熔
炉において所定の調合比にある銅精鉱、固体炭素
質燃料、フラツクス等がきわめて均一に混合され
た状態で装入され、自熔炉内での熱風によつてき
わめて効率的に且つ効果的に反応し、所要の発熱
量が確保される。
自熔炉においては、本件出願人により先に開発
された高温熱風による酸化反応が遂行される。こ
れは、従来の自熔炉においては吹込空気乃至酸素
富化空気の温度は350〜650℃であつたのを、650
℃以上、好ましくは900〜1000℃に維持すること
により銅生産能力を大巾に高めることに成功した
ものであり、本発明において始めて重油燃料転換
策としての微粉炭以外の100%固体炭素質燃料の
使用にきわめて適応性を示すことが見出されたも
のである。高温熱風は、例えば、鉄或いはフエロ
アロイ製錬用熔鉱炉から発生するCOを主体とし
たBガス等の燃焼熱を利用する蓄熱式熱風炉によ
つて容易に得られる。
上述の通り、本発明においては好ましい燃料の
一つとして粉粒コークスを使用すする。コークス
は、従来から揮発力が低く着火点が高い故に高速
燃焼用には用いられないものと思われていた。
又、自熔炉は装入物がシヤフト内を降下する間に
反応を終了すべき炉であるといわれていた。従つ
て、前述したように、従来は自熔炉の鉱油燃焼の
代替用としては専ら微粉炭燃焼が短絡的に考慮さ
れたのである。しかし、本発明者等は、粉粒コー
クスでも、高温熱風により炉内反応速度が十分大
きい条件の下では、自熔炉の補助熱源として十分
に用いることができること、粉粒コークス装入に
より、炉内セトラーの湯面には、粉粒コークスが
浮遊することになるが、浮遊量が増傾向とならな
いように炉内条件と、粉粒コークスの装入量を制
御すれば、安定した操業が続けられることを確認
した。更には、スラグ温度、マツト温度は、従来
の鉱油燃焼の場合に比し若干低目でもタツピング
には差支えないこと(これは炉内のマグネタイト
量減少によると思われる)又、粉粒コークスがセ
トラーの湯面に浮遊していても未燃コークスの排
出は殆どなく、十分に高い熱効率を維持できるこ
とを確認した。
本発明においては最も望ましい態様としては、
自熔炉への銅精鉱・フラツクス装入系統の最も上
流側に紛粒まじりコークスを所定調合比で添加す
ることであり、その場合は銅精鉱・フラツクスと
共に搬送および乾燥され、炉頂の精鉱バーナーを
通して自熔炉内に装入されるが、本発明の範囲は
それのみには限定されず、別系統の粉粒コークス
搬送装入設備を径由したり、専焼バーナーで炉内
に吹込む場合も包含する。
また、粉粒コークスとしては、第1図に生成フ
ローシートを示す沈殿粉コークスが最も好ましい
例であるが、これのみに限られるものではない。
粉粒コークス及び/あるいはサイズ40mm以下の
塊粒粉低質石炭をドライヤーキルンおよび気流輸
送機の上流において銅精鉱・フラツクスなどの装
入系統に添加することにより、以後炉に入るまで
の間に多数の混合チヤンスがあるため、炉に入る
ときは炉内燃焼の良好なな硫化物である銅精鉱と
完全に混合された状態となり、一層迅速に炉内燃
焼することができるようになる。
本発明により従来不可能であつた微粉炭以外の
固体炭素質燃料で全重油量の100%代替を達成す
ることができた。粉粒コークスおよび/あるいは
塊粒粉低質石炭は、何の予備処理も特別な装入設
備も必要とせず銅精鉱と共に自熔炉内に装入さ
れ、きわめて良好な〓−〓形成反応を生じそして
必要な温度を維持する。
これは、650℃以上の高温熱風を使用する自熔
炉において始めて何ら支障を起さず達成すること
ができたものであり、本自熔炉が高温熱風使用に
より反応速度をきわめて迅速化する雰囲気である
ため微粉炭でなくとも塊粉まじりの固体炭素質燃
料を特別の附加設備なしにまた附加処理も要せ
ず、きわめてスムーズに自熔炉内で完全に燃焼で
きたことはむしろ驚くべき効果であつた。
実施例
約3ケ月にわたり自熔炉において重油を使用せ
ず、沈殿粉コークスを使用して操業を行つた。[Table] Specific Description of the Invention Preferred embodiments of the present invention will be described below. FIG. 2 shows the flow until the copper concentrate and solid carbonaceous fuel are charged together into the flash melting furnace. As a blending hopper group 1, a copper concentrate hopper 2, a hopper 3 for granular coke as a representative solid carbonaceous fuel, and a flux hopper 4 are arranged side by side, and each is brought in from an appropriate source. For example, granular coke is carried into the hopper 3 from the granular coke mine 5 by a bucket crane or the like. A cutting device 6 such as a constant feed conveyor is provided below each hopper, and a predetermined amount of raw material is cut out from each hopper. The cut raw material components are transferred to conveyor 8
is fed into the receiving bin 10 by. Conveying equipment such as a chute or a vibrating conveyor may be used instead of the carrying conveyor. The charging material from the receiving bin is fed into the dryer kiln 12 and then into the cage mill 14.
The air flow is transported through the conduit 15 by the air flow. By mixing the solid carbonaceous fuel with the copper concentrate or the like at a stage upstream of pneumatic transport, a very uniformly mixed charge mixture is produced. The pneumatically transported mixture is supplied to the head bin 20 via the chamber 16 and the cyclone group 18. Headbin 20
The charge is introduced from the bottom of the flask through the flask concentrate burner 22, for example by means of a boiler conveyor. Collected dust from the cyclone via the dryer is also charged. The flash furnace 30 includes a shaft 31, a settler 32, and an uptake 33.
It is of a well-known structure and is also equipped with hot air blowing means (not shown). In this way, the copper concentrate, solid carbonaceous fuel, flux, etc. in a predetermined mixing ratio are charged into the flash melting furnace in an extremely uniformly mixed state, and the hot air inside the flash melting furnace allows the melting to be carried out very efficiently and effectively. reacts quickly, ensuring the required calorific value. In the flash-melting furnace, the oxidation reaction using high-temperature hot air, which was previously developed by the applicant, is carried out. This means that in conventional flash melting furnaces, the temperature of the blown air or oxygen-enriched air was 350 to 650°C;
℃ or above, preferably 900 to 1000 ℃, the copper production capacity has been successfully increased significantly, and the present invention is the first to use 100% solid carbonaceous fuel other than pulverized coal as a fuel oil conversion measure. It has been found to be highly adaptable for use. High-temperature hot air can be easily obtained, for example, by a regenerative hot-blast furnace that utilizes the combustion heat of B gas, mainly CO, generated from a smelting furnace for iron or ferroalloy smelting. As mentioned above, in the present invention, granular coke is used as one of the preferred fuels. It has been thought that coke cannot be used for high-speed combustion because of its low volatility and high ignition point.
Also, an flash-melting furnace was said to be a furnace in which the reaction should be completed while the charge is descending within the shaft. Therefore, as mentioned above, pulverized coal combustion has conventionally been considered as an alternative to mineral oil combustion in flash-smelting furnaces. However, the present inventors have discovered that even granular coke can be used as an auxiliary heat source in a flash furnace under conditions where the reaction rate in the furnace is sufficiently high due to high-temperature hot air, and that by charging granular coke, Powdered coke will float on the surface of the settler, but stable operation can be maintained by controlling the furnace conditions and the amount of coke powder charged so that the floating amount does not tend to increase. It was confirmed. Furthermore, even if the slag temperature and mat temperature are slightly lower than in the case of conventional mineral oil combustion, there is no problem in tapping (this is probably due to a decrease in the amount of magnetite in the furnace). It was confirmed that there was almost no discharge of unburned coke even if it was floating on the surface of the hot water, and that a sufficiently high thermal efficiency could be maintained. The most desirable aspect of the present invention is as follows:
Coke powder is added at a predetermined mixing ratio to the most upstream side of the copper concentrate/flux charging system to the flash furnace. Although the coke is charged into the flash-smelting furnace through an ore burner, the scope of the present invention is not limited thereto; it may be blown into the furnace through a separate system of granular coke conveying and charging equipment, or through a dedicated burner. It also includes cases. The most preferable example of the coke powder is precipitated coke whose generation flow sheet is shown in FIG. 1, but the coke is not limited to this. By adding coke powder and/or low-quality coal particles with a size of 40 mm or less to the charging system for copper concentrate, flux, etc. upstream of the dryer kiln and pneumatic conveyor, a large number of coal particles are added to the charging system for copper concentrate, flux, etc. before entering the furnace. Because of this mixing chance, when it enters the furnace, it is completely mixed with the copper concentrate, which is a sulfide that burns well in the furnace, and can be burned in the furnace more quickly. The present invention has made it possible to replace 100% of the total amount of heavy oil with solid carbonaceous fuels other than pulverized coal, which was previously impossible. Powdered coke and/or lumpy powdered low-quality coal are charged into the flash furnace together with the copper concentrate without any pretreatment or special charging equipment, resulting in a very good 〓-〓-forming reaction and Maintain the required temperature. This was achieved for the first time without any problems in a flash melting furnace that uses high-temperature hot air of 650℃ or higher, and this flash melting furnace uses high-temperature hot air to create an atmosphere that extremely speeds up the reaction rate. Therefore, it was a rather surprising effect that solid carbonaceous fuel mixed with lump powder, even if it was not pulverized coal, could be completely burned very smoothly in the flash melting furnace without any special additional equipment or additional treatment. . Example The flash melting furnace was operated for about 3 months using precipitated coke instead of using heavy oil.
【表】
最右欄の従来実績に較べ〓品位も〓中銅品位も
実質上変化なく、安定した自熔炉操業が確保でき
た。
発明の効果
以上、本発明について説明したが、最後に本発
明の効果をまとめると次の通りとなる:
(1) 100%全重油量を代替でき、エネルギーコス
トの削減及び将来のエネルギー事情への対処に
成功した。
(2) 固体炭素質燃料の粉砕等の前処理が不要であ
り、固体炭素質燃料用の別途の装入設備を設け
る必要性を排除しうる。
(3) 微粉炭に比べ安全性が大きく且つ作業環境が
衛生的である。
(4) 沈殿粉コークス等の使用によりコストが安価
である。
(5) 沈殿粉コークスは石炭や石油に較べ揮発分が
少なく、同一発熱量当り燃焼用空気量及び排ガ
ス量が少くてすむ。
(6) 操業中に自熔炉セトラーの湯面に若干の固体
炭素質燃料が浮遊するのが観察されるが、その
浮遊量が増大しない程度に諸条件を管理すれば
支障はなく、却つてスラグ層には対して定常的
に還元作用を及ぼすことによりスラグ中の銅含
有率の低減効果を与えることが期待される。[Table] Compared to the previous results shown in the far right column, there was virtually no change in the grade or middle copper grade, and stable flash-smelting furnace operation was ensured. Effects of the Invention The present invention has been explained above, and the effects of the present invention can be summarized as follows: (1) 100% of the total amount of heavy oil can be replaced, reducing energy costs and contributing to future energy situations. successfully dealt with. (2) Pretreatment such as pulverization of the solid carbonaceous fuel is not required, and the need to provide separate charging equipment for the solid carbonaceous fuel can be eliminated. (3) It is safer than pulverized coal and provides a sanitary working environment. (4) The cost is low due to the use of precipitated coke, etc. (5) Precipitated coke powder has less volatile content than coal or petroleum, and requires less combustion air and exhaust gas for the same calorific value. (6) During operation, a small amount of solid carbonaceous fuel is observed floating on the hot water surface of the flash-smelting furnace settler, but if conditions are controlled to the extent that the floating amount does not increase, there is no problem; on the contrary, the slag It is expected that the layer will have the effect of reducing the copper content in the slag by constantly exerting a reducing action on the layer.
第1図は沈殿粉コークスの生成過程のフローシ
ートであり、そして、第2図は銅精鉱と固体炭素
質燃料を混合下で自熔炉に装入する過程の概略流
れ図である。
1:調合ホツパ群、2:銅精鉱ホツパ、3:粉
粒コークスホツパ、4:フラツクスホツパ、5:
粉粒コークス鉱舎、6:切出秤量装置、8:搬上
コンベア、10:受入ビン、12:ドライヤーキ
ルン、14:ケージミル、15:気流輸送導管、
16:チヤンバ、18:サイクロン、22:精鉱
バーナ、30:自熔炉、31:シヤフト、32:
セツトラー、33:アツプテーク。
FIG. 1 is a flow sheet of the process of producing precipitated coke powder, and FIG. 2 is a schematic flow chart of the process of charging copper concentrate and solid carbonaceous fuel into a flash smelting furnace under mixing. 1: Preparation hopper group, 2: Copper concentrate hopper, 3: Powdered coke hopper, 4: Flux hopper, 5:
Powdered coke building, 6: Cutting and weighing device, 8: Carrying conveyor, 10: Receiving bin, 12: Dryer kiln, 14: Cage mill, 15: Air flow transport conduit,
16: Chamber, 18: Cyclone, 22: Concentrate burner, 30: Flash furnace, 31: Shaft, 32:
Settler, 33: Uptake.
Claims (1)
し、同時に空気あるいは酸素富化空気を650℃以
上に予熱して吹込み、そして補助燃料として固体
炭素質燃料(但し微粉炭を除く)のみを使用し、
100%鉱油を代替したことを特徴とする銅製錬自
熔炉の操業方法。 2 固体炭素質燃料が粉粒コークスおよび/ある
いはサイズ40mm以下の塊粒粉低質石炭である特許
請求の範囲第1項記載の方法。 3 粉粒コークスが沈殿粉コークスである特許請
求の範囲第2項記載の方法。 4 低質石炭が褐炭である特許請求の範囲第2項
記載の方法。 5 粉粒コークスおよび/あるいはサイズ40mm以
下の塊粒粉低質石炭を銅精鉱ドライヤーキルンお
よび気流輸送機より上流において銅精鉱・フラツ
クスなどの装入系統に添加して銅精鉱・フラツク
スなどと共に自熔炉内に装入する特許請求の範囲
第2項記載の方法。[Claims] 1. Copper concentrate, flux, and other charges are charged, and at the same time air or oxygen-enriched air is preheated to 650°C or higher and blown in, and solid carbonaceous fuel (however, (excluding pulverized coal),
A method of operating a copper smelting and flash-melting furnace characterized by replacing 100% mineral oil. 2. The method according to claim 1, wherein the solid carbonaceous fuel is granular coke and/or lump powder low quality coal having a size of 40 mm or less. 3. The method according to claim 2, wherein the coke powder is precipitated coke powder. 4. The method according to claim 2, wherein the low quality coal is lignite. 5. Powdered coke and/or lumpy powdered low-quality coal with a size of 40 mm or less are added to the charging system for copper concentrate, flux, etc. upstream from the copper concentrate dryer kiln and the pneumatic conveyor, and are added together with the copper concentrate, flux, etc. 3. The method according to claim 2, wherein the material is charged into a flash-melting furnace.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15947882A JPS5950132A (en) | 1982-09-16 | 1982-09-16 | Method for operating flash smelting furnace for smelting copper |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15947882A JPS5950132A (en) | 1982-09-16 | 1982-09-16 | Method for operating flash smelting furnace for smelting copper |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5950132A JPS5950132A (en) | 1984-03-23 |
| JPH0224898B2 true JPH0224898B2 (en) | 1990-05-31 |
Family
ID=15694645
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP15947882A Granted JPS5950132A (en) | 1982-09-16 | 1982-09-16 | Method for operating flash smelting furnace for smelting copper |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5950132A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0569794U (en) * | 1991-11-14 | 1993-09-21 | 康勝 丹羽 | Guitar support |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60245735A (en) * | 1984-05-21 | 1985-12-05 | Nippon Mining Co Ltd | Operating method of installation for flash smelting furnace for smelting of copper |
| JP2679105B2 (en) * | 1988-04-27 | 1997-11-19 | 三菱マテリアル株式会社 | Method of smelting metal sulfide ore |
| FI105827B (en) | 1999-05-14 | 2000-10-13 | Outokumpu Oy | Process and device for smelting non-iron metal sulphides in a suspension smelting furnace for the purpose of producing stone having a high content of non-iron metal and slag, which is discarded. |
| FI108542B (en) | 1999-05-14 | 2002-02-15 | Outokumpu Oy | Process for reducing the slag's non-ferrous metal content during the production of non-ferrous metals in a suspension melting furnace |
-
1982
- 1982-09-16 JP JP15947882A patent/JPS5950132A/en active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0569794U (en) * | 1991-11-14 | 1993-09-21 | 康勝 丹羽 | Guitar support |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5950132A (en) | 1984-03-23 |
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