JPS60155631A - Method for recovering zinc from material containing zinc compound - Google Patents
Method for recovering zinc from material containing zinc compoundInfo
- Publication number
- JPS60155631A JPS60155631A JP59011069A JP1106984A JPS60155631A JP S60155631 A JPS60155631 A JP S60155631A JP 59011069 A JP59011069 A JP 59011069A JP 1106984 A JP1106984 A JP 1106984A JP S60155631 A JPS60155631 A JP S60155631A
- Authority
- JP
- Japan
- Prior art keywords
- zinc
- raw material
- dust
- sintering
- compd
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000011701 zinc Substances 0.000 title claims abstract description 68
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 title claims abstract description 23
- 229910052725 zinc Inorganic materials 0.000 title claims abstract description 23
- 239000000463 material Substances 0.000 title claims abstract description 18
- 150000003752 zinc compounds Chemical class 0.000 title claims description 14
- 238000000034 method Methods 0.000 title description 31
- 238000005245 sintering Methods 0.000 claims abstract description 30
- 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 11
- 239000011787 zinc oxide Substances 0.000 claims abstract description 10
- 239000003575 carbonaceous material Substances 0.000 claims abstract description 5
- 150000001875 compounds Chemical class 0.000 claims description 6
- 238000002485 combustion reaction Methods 0.000 claims description 5
- 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 2
- 239000000428 dust Substances 0.000 abstract description 41
- 239000002994 raw material Substances 0.000 abstract description 24
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract description 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract description 6
- 229910052799 carbon Inorganic materials 0.000 abstract description 6
- 238000001704 evaporation Methods 0.000 abstract description 4
- 229910052742 iron Inorganic materials 0.000 abstract description 3
- 238000004898 kneading Methods 0.000 abstract description 3
- 230000009467 reduction Effects 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 11
- 230000008569 process Effects 0.000 description 11
- 229910052751 metal Inorganic materials 0.000 description 10
- 239000002184 metal Substances 0.000 description 10
- 239000004484 Briquette Substances 0.000 description 9
- 238000007670 refining Methods 0.000 description 8
- 239000000126 substance Substances 0.000 description 7
- 239000011248 coating agent Substances 0.000 description 6
- 238000000576 coating method Methods 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 4
- 229910052500 inorganic mineral Inorganic materials 0.000 description 4
- 239000011707 mineral Substances 0.000 description 4
- 235000019738 Limestone Nutrition 0.000 description 3
- 229910000831 Steel Inorganic materials 0.000 description 3
- 230000007613 environmental effect Effects 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 239000006028 limestone Substances 0.000 description 3
- 238000011084 recovery Methods 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- 230000008901 benefit Effects 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 230000002829 reductive effect Effects 0.000 description 2
- 238000009628 steelmaking Methods 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 102000008186 Collagen Human genes 0.000 description 1
- 108010035532 Collagen Proteins 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- FFBHFFJDDLITSX-UHFFFAOYSA-N benzyl N-[2-hydroxy-4-(3-oxomorpholin-4-yl)phenyl]carbamate Chemical compound OC1=C(NC(=O)OCC2=CC=CC=C2)C=CC(=C1)N1CCOCC1=O FFBHFFJDDLITSX-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 238000001354 calcination Methods 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229920001436 collagen Polymers 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000004044 response Effects 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
- C22B19/34—Obtaining 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ヨり発
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 during metal refining processes.
例えば製鉄所で発生する各種ダストは、資源の有効利用
及び環境対策の見地から回収再利用されている。 しか
し、この場合zn化合物が最大の問題となる。 zn@
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には、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
による還元蒸発が代表的なものである。For example, various types of dust generated in steel mills are collected and reused from the standpoint of effective resource use 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 reuse blast furnace dust with a high Zn concentration 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 using a wet cyclone and reductive evaporation using a rotary kiln.
前者の湿式サイクロン法は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″4
)は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910℃であるのを利用し
たもので、ダスト中のznは主として王妃の反応によ−
2て除去される。The former wet cyclone method utilizes the property of Zn to concentrate on the fine grain side, and the removal rate (dezn''4) by this method is
) is about 60-80%. The latter rotary kiln method takes advantage of the fact that the boiling point of metallic Zn is approximately 910°C, and the Zn in the dust is mainly produced by the reaction of the queen.
2 will be removed.
C(8)+CJC9用2GO(Q) (プpドワー戻応
)〜(1)
zno(’8)+、Co(9)+=Zn(9)+1:!
02(ZnOの還元とZnの蒸発)−(2)Zn(f)
+%Q2(9) +=ZnO(S)(Znの酸化と回収
) −+31
0−タリーキルン法によるZnの除去率は80〜95%
である。C(8)+2GO(Q) for CJC9 (pup dowa return response)~(1) zno('8)+, Co(9)+=Zn(9)+1:!
02 (Reduction of ZnO and evaporation of Zn) - (2) Zn(f)
+%Q2(9) +=ZnO(S) (oxidation and recovery of Zn) -+31 The removal rate of Zn by the 0-tally kiln method is 80 to 95%
It is.
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
利益を考慮に入れ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
っているのが現状である。Compared to the rotary kiln method, the wet cyclone method has a lower processing cost, but has the disadvantage of a lower 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 taking into account the benefit of turning iron-containing dust into reduced pellets. For these reasons, the value of dust as a steelmaking resource is low, and currently it is disposed of for environmental reasons rather than from the standpoint of effective resource utilization.
本発明はか覧る諸問題を解決し、安価なダスト処理法(
Zn除去法)t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t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V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 the above 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 the Zn removal method. 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, the present invention not only dezincinates dust generated in steel works, but also dezincinates dust generated from metal refining raw materials or metal refining processes,
It is an object of the present invention to provide a suitable method for recovering zinc.
上記目的の達成のため、本発明は、亜鉛化合物を含有す
る物質に要すれば炭素質物質を混合せしめ、さらにカル
シュラム化合物で被覆した後当該物質を焼結装置内に供
給し、燃焼温度帯域に於て極部的1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、当該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、その状態で当該装
置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 involves mixing a material containing a zinc compound with a carbonaceous material, if necessary, and supplying the material into a sintering device after being coated with a calsulam compound, so that the material is in a combustion temperature range. After metallizing and evaporating the zinc compound in the substance by creating a locally strong reducing atmosphere, zinc oxide is produced by oxidizing the vaporized zinc in the strongly oxidizing atmosphere. , and is characterized in that it is discharged from the device in that state.
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、焼結装置として
通常のDL型焼結機を利用している。In this example t, 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 device.
第1図ゝにおいて、Aはダストの混練、団鉱工程を示し
、Bはp′L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ダスト原料は混練機1に送られ
、必要1こ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
Zn濃度を調整したダストは団鉱機2に送られ団鉱され
る。 さらに団鉱物は団鉱機3に送られカルシュラム化
合物で被覆すれる。 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
があり、石灰石、Fロマイトが好ましい。In FIG. 1, A shows the dust kneading and briquette process, and B shows the sintering and dust dezincing process using a p'L type sintering machine. The Zn-containing dust raw material is sent to a kneader 1, where a carbonaceous reducing agent and a low-Zn iron-containing substance are added as necessary to adjust the carbon-containing concentration and Zn-containing concentration. The dust whose carbon-Zn concentration has been adjusted is sent to a briquette machine 2 and briquettered. Further, the briquette mineral is sent to the briquette machine 3 and coated with a calcilum compound. The coating material is for shielding the zinc-containing dust from a strongly oxidizing atmosphere in the subsequent dezincing process, and naturally needs to have zero or very small zinc content, and limestone and Fromite are preferable.
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5とグレートバー保護のため装入される床敷鉱
6の間に層状に装入される。The aggregate mineral is then sent to a sintering machine, as shown in Figure 1.
It is charged in a layer between the sintering raw material 5 and bedding ore 6 which is charged to protect the great bar.
焼結原料は、まず点火炉16fこよりでその上面が点火
され、その後、焼結機上を移動する過程で装入空気91
こよって燃焼される。 焼結鉱の燃焼帯は上面から下方
に向って、連続的tこ移動し、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 in the ignition furnace 16f, and then, in the process of moving over the sintering machine, the charged air 91
This causes it to be burned. The sintered ore combustion zone continuously moves downward from the upper surface, 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1こ装入された含Zn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, combustion of the Zn-containing dust pellets charged into the bottom layer of the sintering raw material occurs near the ore discharge side.
含Znダストベ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eこ含炭の作用によ=yて上記(1)
(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
しているため2叙上の如く該ペ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に集塵機へ
導ひかれる。When the Zn-containing dust pellet layer starts to burn, as in the rotary kiln method, due to the action of the carbon-containing material, the above (1)
The reaction (2) occurs, and metal zinc is evaporated and removed from the pellets. Here, since the Zn-containing dust pellets are coated with a coating agent, the pellets are shielded from the oxidizing atmosphere as described in Section 2, 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 together with the dust generated during the sintering process to the dust collector.
この際、第1図に示すように、該ダストベレット層が燃
焼している部分(前述の排鉱側に近い所)の排ガスを、
他の排ガスと分離して集1!(集塵機量
12で組線ダストを除去、このダストはダスト原料にリ
サイクル、集塵機18で酸化亜鉛を捕集)することによ
って、Zn濃度の高いダストの歳択的捕集が可能になる
。At this time, as shown in FIG.
Separate it from other exhaust gases and collect it! (The dust collector quantity 12 removes wire assembly dust, this dust is recycled as a dust raw material, and the dust collector 18 collects zinc oxide), thereby making it possible to selectively collect dust with a high Zn concentration.
以下、小型焼結機による含znダストからのZn回収除
去に関する実験結果を示す。 実験後の脱Zn率は下記
の計算式により算出した。Below, experimental results regarding the recovery and removal of Zn from Zn-containing dust using a small sintering machine will be shown. The Zn removal rate after the experiment was calculated using the following formula.
zn:脱Zn前のべL/、ト中のZn(qb)Zn’:
脱zn後の ! (饅ン
T、Fa :脱Zn前のペレット中のT、FJ%)T、
Fe2 :脱Zn後の (%]
原料ダストの団鉱1こはディスクタイプのφ6o。zn: Zn (qb) Zn' in Be L/, To before removing Zn:
After getting off ZN! (Man T, Fa: T, FJ% in pellet before Zn removal) T,
Fe2: After removing Zn (%) One briquette of raw material dust is a disk type φ6o.
造粒機を使用した。 石灰石による被覆は厚さ1酊以下
にするのが好ましい。 実験に用いた小型焼結実験装置
(第2図)#よ実機、焼結機の操業条件を模擬するため
に、焼結層400鰭、空塔速度0.33Nm/sea、
の実機条件下で運転を行なった。 ただ実験後のペレッ
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クラム(焼結原料1こ対して約
2%ン装入し、燃料空気を下方から装入した(第2図膠
原)。A granulator was used. Preferably, the limestone coating is less than 1 inch thick. Small sintering experimental equipment used in the experiment (Fig. 2) To simulate the operating conditions of the actual machine and sintering machine, a sintered layer of 400 fins, a superficial velocity of 0.33 Nm/sea,
The operation was carried out under actual machine conditions. However, considering the ease of collecting pellet samples after the experiment, approximately 100 crumbs of Zn-containing pellets (approximately 2% per 1 sintered raw material) were charged on top of the sintered raw material, and fuel air was charged from below. (Fig. 2 collagen).
脱zn率への含有炭素量、含有zn量、被覆の影響を第
3図1こ示した。 この結果かF)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1こは含炭、含Z
n量の調整が必要であり、被覆処理が必要となるのであ
る。The influence of the amount of carbon contained, the amount of Zn contained, and the coating on the ZN removal rate is shown in FIG. As a result of this, F) There is a strong relationship between the carbon content and Zn content and the Zn removal rate. Therefore, in order to obtain the optimum Zn removal rate as the raw material for blast furnace charging, one
It is necessary to adjust the amount of n, and a coating process is required.
上記実施例では製鉄所発生台Znダストの焼結機1こよ
る脱Zn処理とその回収方法t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に1本発明でい
う焼結装置としては、酸化ペレット焼成設備等もその範
Muこ入ると考えられ、それら装置を使用した場合も本
発明の技術的範囲eこ属することは云うまでもない。In the above example, the Zn removal treatment using a sintering machine 1 for Zn dust generated at a steelworks and its recovery method are explained in detail.As can be inferred from the above experimental results, It is thought that oxidized pellet firing equipment and the like are also included in the calcination equipment, and it goes without saying that the use of such equipment also falls within the technical scope of the present invention.
以上説明した如<21明eこよる含Zn ダストの処理
tこまって、zn濃度の低い焼結鉱を高炉へ供給州来る
ばかりでなく、含Znダスト中のznを安価でかつ容易
eこ回収出来る。As explained above, the processing of Zn-containing dust has become difficult, and not only has sintered ore with a low Zn concentration been supplied to the blast furnace, but also Zn in Zn-containing dust can be recovered easily and cheaply. I can do it.
第1図は本発明のl実施例を示す概略図、第2図は実M
1ご用いた小型焼結実験装置の概略図、第3図は含炭、
含Znベレットを石灰石による被覆した場合の脱zn率
への影響を示すクラ7である。
A・・・混線、団鉱工程 B・・・脱亜鉛工程1・・・
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川Jl塵機 14・
・・フIIIヮー 15・・・煙突 16・・・点火炉
手続補正書
昭和60年4月2S日
特許庁長官 志 賀 学 殿
1、事件の表示
特願昭59−11069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
事件との関係 特許出願人
住 所 東京都千代田区大手町二丁目2番1号名 称
(210)住友重機絨工業株式会社4、代理人
住 所 東京都千代田区大手町二丁目2番1号住友重機
誠工業株式会社内
6、 1lii正の対象
明細書および図面
1)明細書中の特許請求の範囲を以下のように訂正する
。
[炭素質物質および亜鉛化合物を含有する物質を団鉱し
、さらにその団鉱物をカルシ−ラム化合物で被覆した後
、DL酒焼結装置内に供給し、該物質の焼結温度帯域に
於て極部的に!S1還元81III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−tした後強酸化性雰H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、その状態で該焼結装置
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。」
(2)明!JJJ書第2頁第1行目「金属精錬原料」を
「金属精錬原料の前処理工程」と訂正する。
(3)明細書第5頁第15行目「金属[’原料」を「金
属精錬原料の前処理工程」と訂正する。
0)明細書第5頁第4行目乃至第12行目「上記目的達
成の−ため、・・・・・・特徴とするものである。」を
以下のように訂正する。
「上記目的の達成のため、本発明は、亜鉛化合物を含有
する物質に要すれば炭素質物質を混合し、団鉱の後、さ
らにカルシ−ラム化合物で被覆した後当該団鉱物をDL
型貌結装置内に供給し、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U化蒸発分離せしめた後、当該強酸化性雰囲気の
もと蒸気状亜鉛の最北により亜鉛酸化物を生成させ、そ
の状態で当該装置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, and FIG. 2 is an actual M
1 Schematic diagram of the small sintering experimental equipment used, Figure 3 shows the carbon-containing
Figure 7 shows the influence on the Zn removal rate when Zn-containing pellets are covered with limestone. A... Mixed wire, briquette process B... Dezincing process 1...
Kneading machine 2...Bulking machine 3...Bulking machine 4...Sintering raw material hopper 5...Sintering raw material 6...Bed ore?
...Zn-containing dust group mineral 8...Sintered ore 9...
Charged air 10... Wind box 11... Dust collector 12.
・・Dust collector (pre-duster) 13 Kawa Jl dust machine 14・
...FIIIW 15...Chimney 16...Ignition Furnace Procedure Amendment April 2, 1985 Manabu Shiga, Commissioner of the Patent Office1, Indication of Case Patent Application No. 11069-1982, Title of Invention Method 3 of recovering zinc from materials containing zinc compounds;
Relationship with the case of the person making the amendment Patent applicant address 2-2-1 Otemachi, Chiyoda-ku, Tokyo Name
(210) Sumitomo Heavy Industries Makoto Industries Co., Ltd. 4, Agent address: 6, Sumitomo Heavy Industries Makoto Industries Co., Ltd., 2-2-1 Otemachi, Chiyoda-ku, Tokyo, Japan. The scope of claims is amended as follows. [After briquetting a material containing a carbonaceous material and a zinc compound, and further coating the briquette with a calcilum compound, the material is fed into a DL liquor sintering device, and the sintering temperature range of the material is Extremely! The zinc compound in the substance is metallized and evaporated by producing S1 reduction 81III gas, and after separation from the substance, zinc oxide is produced by oxidation of vaporized zinc in a strongly oxidizing atmosphere. A method for recovering zinc from a substance containing a zinc compound, characterized in that zinc is discharged from the sintering device in that state. ” (2) Ming! In the first line of page 2 of the JJJ book, "metal refining raw materials" is corrected to "pretreatment process of metal refining raw materials." (3) On page 5, line 15 of the specification, "metal ['raw material"] is corrected to "pretreatment process for metal refining raw materials." 0) On page 5 of the specification, lines 4 to 12, "In order to achieve the above-mentioned purpose, the present invention is characterized by..." is corrected as follows. "In order to achieve the above object, the present invention mixes a carbonaceous material if necessary with a material containing a zinc compound, and after coating the briquette with a calcium lam compound, the briquette mineral is DL.
The zinc compound in the substance is evaporated and separated into gold by forming a locally strong reducing atmosphere in the sintering temperature range, and then the strongly oxidizing atmosphere is This method is characterized by generating zinc oxide from the northernmost part of the originally vaporized zinc and discharging it from the device in this state. (5) Correct Figure 2 as attached.
Claims (1)
ラム化合物で被債した後、焼結装置内に供給し、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裏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
装置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。After a material containing a carbonaceous material and a zinc compound is bonded with a calcilum compound, the material is fed into a sintering device and a strongly reducing atmosphere is generated locally in the combustion temperature range of the material. The zinc compound inside is metallized and evaporated,
Zinc is extracted from a material containing zinc compounds, characterized in that after separation from the material, zinc oxide is produced by oxidation of vaporized zinc in a strongly oxidizing backing atmosphere and discharged in this state from the sintering device. How to recover.
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59011069A JPS60155631A (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 |
| KR1019850000481A KR910001010B1 (en) | 1984-01-26 | 1985-01-26 | Method for recovering zinc from substances containing a zinc conpound |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59011069A JPS60155631A (en) | 1984-01-26 | 1984-01-26 | Method for recovering zinc from material containing zinc compound |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS60155631A true JPS60155631A (en) | 1985-08-15 |
| JPH0477054B2 JPH0477054B2 (en) | 1992-12-07 |
Family
ID=11767688
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP59011069A Granted JPS60155631A (en) | 1984-01-26 | 1984-01-26 | Method for recovering zinc from material containing zinc compound |
Country Status (2)
| Country | Link |
|---|---|
| JP (1) | JPS60155631A (en) |
| KR (1) | KR910001010B1 (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 |
| JP2020084235A (en) * | 2018-11-20 | 2020-06-04 | 住友金属鉱山株式会社 | Manufacturing method of zinc oxide ore |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2019103432A1 (en) * | 2017-11-27 | 2019-05-31 | 진성복 | Candle for buddhist ceremony |
| KR102007703B1 (en) * | 2017-11-27 | 2019-08-06 | 진성복 | Candle for Buddhism rite |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS57171631A (en) * | 1981-04-16 | 1982-10-22 | Nippon Steel Corp | Spurious particle for sintering iron ore |
| JPS58185728A (en) * | 1982-04-24 | 1983-10-29 | Nisshin Steel Co Ltd | Manufacture of sintered ore for raw material of blast furnace |
-
1984
- 1984-01-26 JP JP59011069A patent/JPS60155631A/en active Granted
-
1985
- 1985-01-26 KR KR1019850000481A patent/KR910001010B1/en not_active Expired
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS57171631A (en) * | 1981-04-16 | 1982-10-22 | Nippon Steel Corp | Spurious particle for sintering iron ore |
| JPS58185728A (en) * | 1982-04-24 | 1983-10-29 | Nisshin Steel Co Ltd | Manufacture of sintered ore for raw material of blast furnace |
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 |
| JP2020084235A (en) * | 2018-11-20 | 2020-06-04 | 住友金属鉱山株式会社 | Manufacturing method of zinc oxide ore |
Also Published As
| Publication number | Publication date |
|---|---|
| KR850005508A (en) | 1985-08-26 |
| JPH0477054B2 (en) | 1992-12-07 |
| KR910001010B1 (en) | 1991-02-19 |
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