JPS60155630A - Method for recovering zinc from material containing zinc compound - Google Patents
Method for recovering zinc from material containing zinc compoundInfo
- Publication number
- JPS60155630A JPS60155630A JP59011068A JP1106884A JPS60155630A JP S60155630 A JPS60155630 A JP S60155630A JP 59011068 A JP59011068 A JP 59011068A JP 1106884 A JP1106884 A JP 1106884A JP S60155630 A JPS60155630 A JP S60155630A
- Authority
- JP
- Japan
- Prior art keywords
- zinc
- dust
- raw material
- sintering
- charged
- 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.)
- Pending
Links
- 239000011701 zinc Substances 0.000 title claims abstract description 69
- 229910052725 zinc Inorganic materials 0.000 title claims abstract description 25
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 title claims abstract description 24
- 239000000463 material Substances 0.000 title claims abstract description 14
- 238000000034 method Methods 0.000 title claims description 31
- 150000003752 zinc compounds Chemical class 0.000 title claims description 13
- 238000005245 sintering Methods 0.000 claims abstract description 35
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims abstract description 20
- 230000001590 oxidative effect Effects 0.000 claims abstract description 12
- 239000011787 zinc oxide Substances 0.000 claims abstract description 10
- 238000001704 evaporation Methods 0.000 claims abstract description 7
- 239000003575 carbonaceous material Substances 0.000 claims abstract description 4
- 239000000126 substance Substances 0.000 claims description 12
- 238000002485 combustion reaction Methods 0.000 claims description 7
- 230000008020 evaporation Effects 0.000 claims description 4
- 230000003647 oxidation Effects 0.000 claims description 3
- 238000007254 oxidation reaction Methods 0.000 claims description 3
- 238000000926 separation method Methods 0.000 claims description 3
- 238000001465 metallisation Methods 0.000 claims description 2
- 239000000428 dust Substances 0.000 abstract description 44
- 239000002994 raw material Substances 0.000 abstract description 25
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract description 8
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract description 7
- 229910052799 carbon Inorganic materials 0.000 abstract description 7
- 229910052742 iron Inorganic materials 0.000 abstract description 3
- 238000004898 kneading Methods 0.000 abstract description 3
- 239000003638 chemical reducing agent Substances 0.000 abstract description 2
- 239000011362 coarse particle Substances 0.000 abstract 1
- 239000002912 waste gas Substances 0.000 abstract 1
- 239000008188 pellet Substances 0.000 description 12
- 239000004484 Briquette Substances 0.000 description 7
- 238000007670 refining Methods 0.000 description 7
- 239000002184 metal Substances 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 5
- 239000011248 coating agent Substances 0.000 description 5
- 238000000576 coating method Methods 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- 229910000831 Steel Inorganic materials 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 230000007613 environmental effect Effects 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 229910052500 inorganic mineral Inorganic materials 0.000 description 3
- 239000011707 mineral Substances 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- 238000010586 diagram Methods 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 238000009628 steelmaking Methods 0.000 description 2
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- 235000019738 Limestone Nutrition 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
- 229910000514 dolomite Inorganic materials 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B19/00—Obtaining zinc or zinc oxide
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P10/00—Technologies related to metal processing
- Y02P10/20—Recycling
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Manufacture And Refinement Of Metals (AREA)
Abstract
Description
【発明の詳細な説明】
この発明は、金属精錬原料あるいは金属精錬工程より発
生するダスト等の亜鉛化合物を含有する物質から亜鉛を
回収する方法に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for recovering zinc from materials containing zinc compounds, such as metal refining raw materials or dust generated from metal refining processes.
例えば製鉄所で発生する各種ダストは、*源の有効利用
及び環境対策の見地から回収再利用さnている。 しか
し、この場合、zn化合物が最大の問題となる。 Zn
濃度の低いダストは直接、焼結機、転炉・、電気炉等へ
供給される場合もあるが、Zn濃度の高い高炉ダスト等
を製鉄原料として再利用するためをこけ、前処理として
脱Zn 処理を施す必要がある。 現在、脱znの処理
法としては湿式サイクロンtこよる分級分離、ロータリ
ーキルンtこよる還元蒸発が代表的なものである。For example, various types of dust generated at steel plants are collected and reused from the standpoint of effective resource utilization and environmental protection. However, in this case, the zn compound poses the biggest problem. Zn
In some cases, dust with a low concentration is directly supplied to a sintering machine, converter, electric furnace, etc., but in order to avoid blast furnace dust with a high Zn concentration and reusing it as a raw material for steelmaking, it is necessary to remove Zn as a pretreatment. It is necessary to carry out processing. At present, typical methods for removing Zn include classification separation using a wet cyclone and reduction evaporation using a rotary kiln.
前者ノ湿式すイクロン法はznが細粒側に濃縮する性質
を利用したもので、この方法による除去率(脱Zn率戸
よ60〜80%程度である。 後者のロータリーキルン
法は、金属Znの沸点が約9 ’l O’0 であるの
を利用したもので、ダスト中のznは主として下記の反
応によって除去される。The former wet cyclone method takes advantage of the property of Zn concentrating on the fine grain side, and the removal rate (removal rate of Zn) by this method is about 60 to 80%. This method takes advantage of the fact that the boiling point is about 9'l O'0, and zn in the dust is mainly removed by the following reaction.
C(S)−1−002(g)=200(す)(ブルドワ
ー反応) −(11
znO(S〕+Co(g )=Zn(g)+C02(1
/) ’(ZnOの還元とZnの蒸発)−(2)Zn(
Q)+%02(す)=ZnO(S )(Znの酸化と回
収) −+3]
ロータリーキルン法によるZn の除去率は80〜95
%である。C(S)-1-002(g)=200(su)(Bourdower reaction)-(11 znO(S)+Co(g)=Zn(g)+C02(1
/) '(Reduction of ZnO and evaporation of Zn) - (2) Zn(
Q)+%02(S)=ZnO(S) (oxidation and recovery of Zn) -+3] The removal rate of Zn by rotary kiln method is 80-95
%.
湿式サイクロン法はロータリーキルン法1こ較べて処理
コストは低いが、zn除去率が低い欠点がある。 これ
に較べてロータリーキルン法はZn除去率は高いが処理
コストが高く含鉄ダストが還元ベレットになるという利
益を考慮tこ入わても尚採算が取れない。 このような
理由から製鉄資源としてのダストの価値評価は低く、資
源の有効利用の見地からよりむしろ、環境対策上処理を
行すているのが現状である。Although the wet cyclone method has a lower processing cost than the rotary kiln method, it has the disadvantage of a low Zn removal rate. In comparison, the rotary kiln method has a high Zn removal rate, but the processing cost is high and it is still unprofitable even considering the benefit of turning iron-containing dust into reduced pellets. For these reasons, the value of dust as a steelmaking resource is low, and the current situation is that dust is disposed of for environmental reasons rather than from the standpoint of effective resource utilization.
本発明はか\る諸問題を解決し、安価なダスト処理法(
Zn除去法)1こ基づくダストの有効利用及び環境対策
を兼ねそなえた亜鉛回収方法を提供することを目的とす
るものであり、本発明の実施eこより、ダストから除去
された亜鉛を亜鉛化合物として高濃度で捕集し、後工程
の金属亜鉛精錬へ付加価値の高い原料として供給するこ
とを可能とするものである。 さらに本発明では製鉄所
で発生するダストの脱亜鉛のみならず金属精錬原料ある
いは金属精錬工程より発生するダストを脱亜鉛処理し亜
鉛を回収するのtこ好適なる亜鉛回収方法を提供するこ
とを目的とする。The present invention solves these problems and provides an inexpensive dust treatment method (
The purpose of this invention is to provide a method for recovering zinc that combines the effective use of dust and environmental measures based on Zn removal method (1). This makes it possible to collect highly concentrated zinc and supply it as a high value-added raw material to the subsequent metal zinc refining process. Furthermore, it is an object of the present invention to provide a method for recovering zinc that is suitable for not only dezincing dust generated in steel works but also dezincing raw materials for metal refining or dust generated from metal refining processes and recovering zinc. shall be.
上記目的の達成のため、本発明は、亜鉛化合物を含有す
る物質tこ要すれば炭素質物質を混合せしめ、当該物質
を焼結機内の床敷鉱上に供給し、燃焼温度帯域に於て極
部的eこ強還元雰囲気を生成することにより当該物質中
の亜鉛化合物を金属化蒸発分離せしめた後、強酸化性雰
囲気のもと蒸気状亜鉛の酸化により亜鉛酸化物を生成さ
せ、その状態で当該焼結機から排出することを特徴とす
るものである。In order to achieve the above object, the present invention mixes a material containing a zinc compound with a carbonaceous material if necessary, supplies the material onto a bedding ore in a sintering machine, and injects the material into a combustion temperature range. After metallizing and evaporating the zinc compounds in the substance by creating a locally strong reducing atmosphere, zinc oxide is produced by oxidizing the vaporized zinc in a strong oxidizing atmosphere, and the state The sintering machine is characterized by being discharged from the sintering machine.
以下本発明の一実施例に基づき説明する。An explanation will be given below based on one embodiment of the present invention.
本実施例tこおいては亜鉛化合物を含有する物質として
製鉄所から排出されるダストを選び、焼結機として通常
のDL型焼結機を利用している。In this embodiment, dust discharged from a steel mill is selected as the substance containing zinc compounds, and a normal DL type sintering machine is used as the sintering machine.
第1図tこおいて、Aはダストの混錬、団鉱工程を示し
、BはDL型焼結機tこよる焼結およびダストの脱亜鉛
工程を示す。 含Znダスト原料は混線機lに送られ必
要に応じて炭素質還元剤、低Zn含鉄物質が添加され、
含炭素濃度、含zn濃度の調整を行なう。 炭素、 Z
n濃度を調整したダストは団鉱機2に送られ団鉱される
。 さらに被覆を施す場合は団鉱機3に送られ、低zn
物質で団鉱機2による団鉱物を被覆する。In FIG. 1, A shows the dust kneading and briquetting process, and B shows the sintering and dust dezincing process using a DL type sintering machine. The Zn-containing dust raw material is sent to the mixer 1, where a carbonaceous reducing agent and a low-Zn iron-containing substance are added as necessary.
The carbon-containing concentration and the Zn-containing concentration are adjusted. Carbon, Z
The dust with adjusted n concentration is sent to the briquetting machine 2 and is briquetted. When further coating is applied, it is sent to the briquette machine 3, and the low zn
Covering the briquette by the briquette machine 2 with the substance.
被覆剤は、後段の脱亜鉛工程において亜鉛含有ダストを
強酸化性雰囲気から遮断するためのものであり、当然亜
鉛含有量が零か極少量である必要があるが、石灰石、ド
ロマイトが好ましい。 続いて団鉱物は焼結機へ送られ
、第1図に示すように、焼結原料すとグレートバー保護
のため装入される床敷鉱6の間に層状tこ装入される。The coating material is for shielding the zinc-containing dust from the strongly oxidizing atmosphere in the subsequent dezincing process, and naturally needs to have zero or a very small amount of zinc, but limestone and dolomite are preferable. Subsequently, the aggregate mineral is sent to a sintering machine, and as shown in FIG. 1, it is charged in a layer between the sintering raw material and bedding ore 6 which is charged to protect the grate bar.
焼結原料は、まず点火炉16によってその上面が点火さ
れ、その後、焼結機上を移動する過程で装入空気9によ
って燃焼される。 焼結鉱の燃焼帯は上面から下方に向
って連続的に移動し、最下層の燃焼が完了した後、冷却
機へ排出される。The upper surface of the sintering raw material is first ignited by the ignition furnace 16, and then it is combusted by the charge air 9 in the process of moving over the sintering machine. The sintered ore combustion zone moves continuously from the upper surface downward, and after the combustion of the lowest layer is completed, it is discharged to the cooler.
このため焼結原料の最下層に装入された含7.nダスト
ベレットの燃焼は排鉱側に近い所で起こる。For this reason, 7. Combustion of n dust pellets occurs close to the ore discharge side.
含Znダストペレット層が燃焼を開始すると、ロータリ
ーキルン法と同様1こ、含炭の作用1こよって上記fl
+ +2)の反応が起りペレットから金属亜鉛が蒸発除
去される。 ここで含Znダストペレットを被覆剤で被
覆している場合には、以上の如く該ベレットは酸化性雰
囲気から遮断され、上記(2)の反応が促進される。
蒸発したZnは酸化気流中で上記(3)の反応によって
酸化亜鉛となり、焼結過程で発生したダストと一諸1こ
集塵機へ導ひかれる。When the Zn-containing dust pellet layer starts to burn, the above-mentioned fl
+ +2) reaction occurs and metallic zinc is evaporated and removed from the pellet. When the Zn-containing dust pellets are coated with a coating agent, the pellets are shielded from the oxidizing atmosphere as described above, and the reaction (2) above is promoted.
The evaporated Zn becomes zinc oxide through the reaction (3) above in the oxidizing gas flow, and is led to the dust collector along with the dust generated during the sintering process.
この際、第1図に示すように当該ダストベレン1層が燃
焼している部分(前述の排鉱側1こ近い所)の排ガスを
、他の排ガスと分離して集塵(集塵機粒
12で粗剛ダストを除去、このダストはダスト原料にリ
サイクル、集塵機13で酸化亜鉛を捕集)′することに
よ・コて、zn濃度の高いダストの選択的捕集が可能に
なる。At this time, as shown in Fig. 1, the exhaust gas in the part where the first layer of the dust berene is burning (the place near the aforementioned ore discharge side) is separated from other exhaust gases and collected (roughly coarsened with dust collector particles 12). By removing the hard dust, recycling this dust as a dust raw material, and collecting zinc oxide with the dust collector 13, it becomes possible to selectively collect dust with a high ZN concentration.
以下、小型焼結機1こよる含Znダストからのzn用収
除去に関する実験結果を示す。 実験後の脱In率は下
記の計算式tこより算出した。Below, experimental results regarding the removal of Zn from Zn-containing dust using one small sintering machine will be shown. The In removal rate after the experiment was calculated using the following calculation formula.
Zn: 脱Zn前のペレット中のZn(%)zn’ ;
脱Zn後の 〃 (%)
T、Fe :脱Zn前のペレット中のT、Fe(%ンT
、Fθ′:脱zn後の (%)
原料ダストの団鉱にはディスクタイプのφ600造粒機
を使用した。実験tこ用いた小型焼結実験装置(第2図
)は実機焼結機の操業条件を模擬するために焼結層40
0mW、空塔速度0.33Nm/8θC1の実機条件下
で運転を行なった。 ただ実験後のベレットサンプルの
採取の容易さを考えて、含Znペレットを焼結原料上面
に約100グラム(焼結原料に対して約2%)装入し、
燃焼内空気を下方から装入した(第2図参照ン。Zn: Zn (%) zn' in pellet before Zn removal;
〃 (%) T, Fe after removing Zn: T, Fe (%) in the pellet before removing Zn
, Fθ′: (%) after deznization A disk type φ600 granulator was used for briquetting the raw material dust. The small sintering experimental equipment used in this experiment (Figure 2) was designed to simulate the operating conditions of an actual sintering machine.
Operation was performed under actual machine conditions of 0 mW and superficial velocity of 0.33 Nm/8θC1. However, considering the ease of collecting pellet samples after the experiment, approximately 100 grams of Zn-containing pellets (approximately 2% of the sintered raw material) were charged on top of the sintered raw material.
Air within the combustion chamber was charged from below (see Figure 2).
脱Zn率への含有炭素量、含有Zn量、被覆の影響を第
3図に示した。 この結果から含炭、含zn量と脱zn
率は強い関係を持っている。このため高炉装入原料とし
ての最適脱Zn率を得るために、は含炭1合Zn量の調
整が必要であり、場合によっては被覆処理も必要となる
のである。FIG. 3 shows the effects of carbon content, Zn content, and coating on the Zn removal rate. From these results, we can determine the carbon content, Zn content, and Zn removal.
rates have a strong relationship. Therefore, in order to obtain the optimum Zn removal rate as a raw material to be charged into a blast furnace, it is necessary to adjust the amount of carbon-containing Zn, and in some cases, a coating treatment is also required.
本発明は以上のような構成となりており、床敷鉱と焼結
鉱との間に含亜鉛物質を供給することにより、当該物質
が床敷鉱と焼結鉱との間のバインダーとして作用し、焼
結機より排出される製品と一体化され製品粒度を高める
結果となる。 さらに、焼結機の焼結原料最下部の燃焼
帯のみでZnの蒸発が起るため以上の如き選択集塵が可
能となるほか、原料内でのZnの再蒸着を起すおそれが
ない。The present invention has the above configuration, and by supplying a zinc-containing substance between bedding ore and sintered ore, the substance acts as a binder between bedding ore and sintered ore. , it is integrated with the product discharged from the sintering machine, resulting in an increase in the product particle size. Furthermore, since Zn evaporates only in the combustion zone at the bottom of the sintered raw material of the sintering machine, selective dust collection as described above is possible, and there is no risk of redeposition of Zn within the raw material.
なお、上記実施例では製鉄所発生台Znダストの焼結機
による脱Zn処理とその回収方法eこつぃて説明をして
いるが、上記の実験結果から類推できるようtこ本発明
でいう焼結機としては、酸化ぺレット焼成設備等もその
範噴に入ると考えられ、そわら装置を使用した場合も本
発明の技術的範囲に属することは云うまでもない。In addition, in the above example, the Zn removal treatment using a sintering machine for Zn dust generated at a steelworks and its recovery method are explained in detail, but as can be inferred from the above experimental results, As a condensing machine, oxidized pellet firing equipment and the like are considered to fall under this category, and it goes without saying that the use of a sowing machine also falls within the technical scope of the present invention.
以上説明した如く、本発明1こよる含Znダストの処理
1こよりて、zn濃度の低い焼結鉱を高炉に供給できる
ばかりでなく、含Znダスト中のZnを安価でかつ容易
tこ回収できる。As explained above, by processing Zn-containing dust according to the present invention 1, not only can sintered ore with a low Zn concentration be supplied to a blast furnace, but also Zn in the Zn-containing dust can be easily recovered at low cost. .
第1図は本発明のl実施例を示す概略図、第2図は実験
に用いた小型焼結実験装置の概略図、第3図は含炭、含
Znペレットを石灰6會こより被覆した場合の脱Zn率
への影響を示すグラフである。
A・・・混線、団鉱工程 B・・・脱亜鉛工程!・・・
混練機 2・・・団鉱機 3・・・団鉱機 4・・・焼
結原料ホッパー 5・・・焼結原料 6・・・床敷鉱?
・・・含znダスト団鉱物 8・・・焼結鉱 9・・・
装入空気 10・・・風箱 11・・・集塵機 12・
・・集塵機(プレダスタ−) 13・・・集塵機 14
・・・プロワ−15・・・煙突 16・・・点火炉
第1頁の続き
@Int、C1,’ 識別記号 、庁内整理番号C22
B 19/34 7128−4K[相]発 明 者 永
易 只 光 新居浜市惣関町製造所内
0発 明 者 杉 森 誠 二 新居浜市惣関町製造所
内
°5番2号 住友重機械工業株式会社新居浜°5番2号
住友重機械工業株式会社新居浜手続補正書
昭和60年4月25日
特許庁長官 志 賀 学 殿
1、事件の表示
特願昭59−11068号
2、発明の名称
亜鉛化合物を含有する物質から亜鉛を回収する方法3、
補正をする者
名 称 (210)住友重機械工業株式会社4、代理人
(1) 明細書中の特許請求の範囲を以下のように訂正
するO
[炭素質物質および亜鉛化合物を含有する物質を団鉱し
、その団鉱物をDL型焼結機内の床敷鉱上に供給し、該
物質の焼結温度帯域に於て極部的に強還元雰囲気を生成
することにより該物質中の亜鉛化合物を金属化蒸発せし
め該物質から分離した後強酸化性雰囲気のもと蒸気状亜
鉛の酸化により亜鉛酸化物を生成させその状態で該焼結
機から出することを特徴とする亜鉛化合物を含有する物
質から亜鉛を回収する方法。」
(2)明細書第1頁第15行目「金属精錬原料」を「金
線原料の前処理工程」と訂正する。
III書第4頁給14行目「金属精錬原料」を「余録原
料の前処理工程」と訂正する。
細書第5頁第3行目乃至第11行目「上記目的のため、
・・・・・・特徴とするものである。コを以下うに訂正
する。
「上記目的の達成のため、本発明は、亜鉛化合を含有す
る物質に要すれば炭素質物質を混合し、団鉱の後、当該
団鉱物をDL型焼結機内の床敷鉱上に供給し、焼結温度
帯域に於て極部的に強還元雰囲気を生成することにより
当該物質中の亜鉛化合物を金属化蒸発分離せしめた後、
強酸化性雰囲気のもと蒸気状亜鉛の酸化により亜鉛酸化
物を生成させ、その状態で当該焼結機から排出すること
を特徴とするものである。
(5)第2図を添付のように訂正する。Fig. 1 is a schematic diagram showing an embodiment of the present invention, Fig. 2 is a schematic diagram of a small sintering experimental device used in the experiment, and Fig. 3 is a case in which carbon-containing and Zn-containing pellets are coated with 6 pieces of lime. It is a graph showing the influence on the Zn removal rate. A... Mixed wires, briquette process B... Dezincing process! ...
Kneading machine 2...Bulking machine 3...Bulking machine 4...Sintering raw material hopper 5...Sintering raw material 6...Bed ore?
...Zn dust-containing group mineral 8...Sintered ore 9...
Charged air 10... Wind box 11... Dust collector 12.
...Dust collector (pre-duster) 13...Dust collector 14
...Plower 15...Chimney 16...Continuation of ignition furnace page 1 @Int, C1,' Identification symbol, internal reference number C22
B 19/34 7128-4K [Phase] Inventor Tadamitsu Eiji Soseki-cho, Niihama City 0 Inventor Seiji Sugimori No. 5-2, Soseki-cho Factory, Niihama City Sumitomo Heavy Industries, Ltd. Niihama°5-2 Sumitomo Heavy Industries Co., Ltd. Niihama Procedural Amendment April 25, 1985 Manabu Shiga, Commissioner of the Patent Office 1, Indication of Case Patent Application No. 11068-1982 2, Name of Invention Zinc Compound Method 3 of recovering zinc from contained substances,
Name of the person making the amendment (210) Sumitomo Heavy Industries, Ltd. 4, Agent (1) Amend the claims in the specification as follows. The zinc compounds in the substance are briquetted and the briquette mineral is supplied onto the bedding ore in a DL type sintering machine, and a strong reducing atmosphere is generated locally in the sintering temperature range of the substance. After metallization and evaporation and separation from the substance, zinc oxide is produced by oxidation of vaporized zinc in a strongly oxidizing atmosphere, and the zinc compound is discharged from the sintering machine in this state. A method of recovering zinc from materials. (2) On page 1, line 15 of the specification, "metal refining raw materials" is corrected to "pretreatment process for gold wire raw materials." Book III, page 4, line 14, ``metal refining raw materials'' is corrected to ``pretreatment process for additional raw materials.'' Page 5, lines 3 to 11 of the specification: ``For the above purpose,
...It is a feature. Correct this as follows. "In order to achieve the above object, the present invention mixes a carbonaceous material with a material containing a zinc compound, if necessary, and after briquette, supplies the briquette onto the bedding ore in a DL type sintering machine. After metallizing and evaporating the zinc compound in the substance by generating a strongly reducing atmosphere locally in the sintering temperature range,
This method is characterized in that zinc oxide is produced by oxidizing vaporized zinc in a strongly oxidizing atmosphere, and is discharged in this state from the sintering machine. (5) Correct Figure 2 as attached.
Claims (1)
の床敷鉱上に供給し、該物質の燃焼温度帯域に於て極部
的に強還元雰囲気を生成することにより該物質中の亜鉛
化合物を金属化蒸発せしめ該物質から分離した後強酸化
性雰囲気のもと蒸気状亜鉛の酸化tこより亜鉛酸化物を
生成させその状態で該焼結機から排出することを特徴と
する亜鉛化合物を含有する物質から亜鉛を回収する方法
。A material containing a carbonaceous material and a zinc compound is supplied onto the bedding ore in a sintering machine, and a strongly reducing atmosphere is generated locally in the combustion temperature range of the material, thereby reducing the zinc compounds in the material. Contains a zinc compound characterized in that after metallization evaporation and separation from the substance, zinc oxide is produced from the oxidation of vaporized zinc in a strongly oxidizing atmosphere and discharged in that state from the sintering machine. method of recovering zinc from materials that contain it.
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59011068A JPS60155630A (en) | 1984-01-26 | 1984-01-26 | Method for recovering zinc from material containing zinc compound |
| DE8585100674T DE3564966D1 (en) | 1984-01-26 | 1985-01-23 | A method for recovering zinc from substances containing a zinc compound |
| CA000472631A CA1239020A (en) | 1984-01-26 | 1985-01-23 | Method for recovering zinc from substances containing a zinc compound |
| EP19850100674 EP0150805B1 (en) | 1984-01-26 | 1985-01-23 | A method for recovering zinc from substances containing a zinc compound |
| US06/695,030 US4595574A (en) | 1984-01-26 | 1985-01-25 | Method for recovering zinc from substances containing a zinc compound |
| KR1019850000480A KR850005507A (en) | 1984-01-26 | 1985-01-26 | Recovery of zinc from substances containing zinc compounds |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59011068A JPS60155630A (en) | 1984-01-26 | 1984-01-26 | Method for recovering zinc from material containing zinc compound |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS60155630A true JPS60155630A (en) | 1985-08-15 |
Family
ID=11767662
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP59011068A Pending JPS60155630A (en) | 1984-01-26 | 1984-01-26 | Method for recovering zinc from material containing zinc compound |
Country Status (2)
| Country | Link |
|---|---|
| JP (1) | JPS60155630A (en) |
| KR (1) | KR850005507A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008045159A (en) * | 2006-08-11 | 2008-02-28 | Jfe Steel Kk | Dust sintering method and sintering machine |
| JP2012241205A (en) * | 2011-05-16 | 2012-12-10 | Nippon Steel Engineering Co Ltd | Method for reduction treatment of metal oxide |
-
1984
- 1984-01-26 JP JP59011068A patent/JPS60155630A/en active Pending
-
1985
- 1985-01-26 KR KR1019850000480A patent/KR850005507A/en not_active Abandoned
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008045159A (en) * | 2006-08-11 | 2008-02-28 | Jfe Steel Kk | Dust sintering method and sintering machine |
| JP2012241205A (en) * | 2011-05-16 | 2012-12-10 | Nippon Steel Engineering Co Ltd | Method for reduction treatment of metal oxide |
Also Published As
| Publication number | Publication date |
|---|---|
| KR850005507A (en) | 1985-08-26 |
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