JPS61151027A - Selective leaching of antimony and/or arsenic - Google Patents

Selective leaching of antimony and/or arsenic

Info

Publication number
JPS61151027A
JPS61151027A JP27213084A JP27213084A JPS61151027A JP S61151027 A JPS61151027 A JP S61151027A JP 27213084 A JP27213084 A JP 27213084A JP 27213084 A JP27213084 A JP 27213084A JP S61151027 A JPS61151027 A JP S61151027A
Authority
JP
Japan
Prior art keywords
arsenic
antimony
leaching
refinery
sulfide
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
Application number
JP27213084A
Other languages
Japanese (ja)
Inventor
Shuichi Oto
修一 大戸
Kaname Hirano
平野 要
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.)
Eneos Corp
Original Assignee
Nippon 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 Nippon Mining Co Ltd filed Critical Nippon Mining Co Ltd
Priority to JP27213084A priority Critical patent/JPS61151027A/en
Publication of JPS61151027A publication Critical patent/JPS61151027A/en
Pending legal-status Critical Current

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  • Inorganic Compounds Of Heavy Metals (AREA)
  • Manufacture And Refinement Of Metals (AREA)

Abstract

PURPOSE:To enable the selective leaching of antimony and arsenic, by treating a substance containing antimony and/or arsenic with sodium hydrosulfide. CONSTITUTION:A substance containing antimony and/or arsenic such as the cupellation dust, refinery dust, refinery slime, etc., in copper refinery, is treated with sodium hydrosulfide. The leaching temperature in the above treatment is preferably 70-90 deg.C, and the concentration of the sodium hydrosulfide in the leaching liquid is preferably 150-250g/l. Antimony can be recovered in the form of antimony sulfide by adjusting the pH of the leached liquid to 5-8 with an acid, and then arsenic is recovered as arsenic sulfide by lowering the pH to <=2 with additional acid. Even in the refinery of copper or lead ore having high content of impurities such as antimony, arsenic, etc., the removal of the impurities from the system can be facilitated and the process can be operated in high efficiency.

Description

【発明の詳細な説明】 本発明は、アンチモン及び又はひ素の選択浸出方法に関
する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for selective leaching of antimony and/or arsenic.

従来、アンチモン及び又はひ素を含み他の金属等を含む
物質から、効率良く選択的にアンチモン及び又はひ素を
除く方法は、開示されていない。
Conventionally, a method for efficiently and selectively removing antimony and/or arsenic from a substance containing antimony and/or arsenic and other metals has not been disclosed.

特に、アンチモ/、ひ素を同時に含む9例えば銅製錬に
おける分銀煙灰、製錬ダスト、製錬スライム等の効率的
処理方法が開示されておらず、よシ好ましい方法が望ま
れている。
In particular, there is no disclosure of an efficient method for treating silver smoke ash, smelting dust, smelting slime, etc. in copper smelting, which simultaneously contain antimony/arsenic, and a more preferable method is desired.

一般に行われる浸出分離方法としては、塩酸。A commonly used leaching separation method is hydrochloric acid.

硫酸、カセイソーダ等による浸出があるが、これらの方
法では鉛、ビスマス等が、同時に浸出されたシ、また浸
出率がすべての重金属に対し悪い等であシ、好ましい方
法で々かった。
Leaching with sulfuric acid, caustic soda, etc. is available, but these methods simultaneously leached out lead, bismuth, etc., and the leaching rate was poor for all heavy metals, so these methods were not preferred.

本発明は、上記の従来技術の欠点を排除するものである
The present invention eliminates the drawbacks of the prior art described above.

即ち、アンチモン及び又はひ素を含む物質の処理方法に
おいて、水硫化ソーダによ多処理するアンチモン及び又
はひ素の選択浸出方法に関する。
That is, the present invention relates to a method for selectively leaching antimony and/or arsenic, which involves extensive treatment with sodium hydrogen sulfide in a method for treating substances containing antimony and/or arsenic.

さらに2本発明の実施態様として浸出温度が70〜90
℃であるアンチモン及び又はひ素の選択浸出方法を提供
する。
Furthermore, in two embodiments of the present invention, the leaching temperature is 70 to 90.
Provided is a method for selective leaching of antimony and/or arsenic at 0.degree.

また、他の実施態様としては、浸出液の水硫化ソーダ及
び又は硫化ソーダの濃度が150゛〜2 s o t/
lであるアンチモン及び又はひ素の選択浸出方法を提供
する。
In another embodiment, the concentration of sodium bisulfide and/or sodium sulfide in the leachate is 150° to 2 s o t/
A method for selective leaching of antimony and/or arsenic is provided.

以下本発明について詳細に説明する。The present invention will be explained in detail below.

本発明における対象物質は、アンチモン及び又はひ素を
含有する物質すべてである。
Target substances in the present invention are all substances containing antimony and/or arsenic.

これらの物質の具体的な例としては、銅製錬における分
銀煙灰、製錬ダスト、製錬スライム等がある。
Specific examples of these substances include silver smoke ash from copper smelting, smelting dust, and smelting slime.

上記物質の通常のアンチモン及び又はひ素の含有量はア
ンチモン5〜40嘩、ひ素2〜30−である。
The usual antimony and/or arsenic content of the above materials is 5 to 40 parts antimony and 2 to 30 parts arsenic.

アンチモン及び又はひ素を含有する物質を効率よく浸出
するためpHが10〜20になるように水硫化ソーダ及
び又は硫化ソーダを添加する。
In order to efficiently leach out substances containing antimony and/or arsenic, sodium bisulfide and/or sodium sulfide is added so that the pH becomes 10 to 20.

また、浸出液の水硫化ソーダ及び又は硫化ソーダの濃度
は150〜250 fitの範囲が好ましく、浸出温度
は70〜90℃が好ましい。
Further, the concentration of sodium bisulfide and/or sodium sulfide in the leaching solution is preferably in the range of 150 to 250 fit, and the leaching temperature is preferably 70 to 90°C.

パルプ濃度は、100〜250 f/を程度が好ましい
The pulp density is preferably about 100 to 250 f/.

攪拌速度は、400〜1000 R1’M程度が好まし
い。
The stirring speed is preferably about 400 to 1000 R1'M.

上記処理によシ、アンチモン、砒素が選択的に浸出され
る。浸出液に酸を加え、pH−5〜8にすることにより
硫化アンチモンとしてアンチモノを回収し、その後さら
に醸を加えることによりpH=2以下とし、硫化砒素と
して砒素を回収することが出来る。また他の回収方法2
例えば、イオン交換樹脂による回収あるいは溶媒抽出を
行うととくよシ回収しても良い。
The above treatment selectively leaches out antimony, arsenic, and arsenic. Antimony can be recovered as antimony sulfide by adding acid to the leachate to bring the pH to -5 to 8, and then the pH can be lowered to 2 or less by further adding brewing to recover arsenic as arsenic sulfide. Another collection method 2
For example, recovery using an ion exchange resin or solvent extraction may be performed.

以上のように本発明を実施することKよシ。The present invention can be carried out as described above.

以下の効果を得る゛ことができる。You can obtain the following effects.

(1)  アンチモノ及び又は砒素の選択的抽出が可能
である。
(1) Selective extraction of antimono and/or arsenic is possible.

(2)  鋼及び鉛製錬において、アンチモン、砒素等
の不純物の多い鉱石であっても不純物の系外除去が容易
となシ、効率の良い操業が可能である。
(2) In steel and lead smelting, even if the ore contains many impurities such as antimony and arsenic, it is easy to remove the impurities outside the system, and efficient operations are possible.

実施例1 銅製錬における分銀煙灰、製錬ダスト、製錬スライムを
混ぜた製錬中間物品(Slt 21.6%、 Ag5.
19s、 Bi 17.8%、 Ou 4.B61r、
 Pb 15.6To、 Ag [LO1*。
Example 1 A smelting intermediate product (Slt 21.6%, Ag5.
19s, Bi 17.8%, Ou 4. B61r,
Pb 15.6To, Ag [LO1*.

T、87.23%)を水硫化ソーダ液によシ浸出処理を
行った。
T, 87.23%) was leached with a sodium hydrogen sulfide solution.

MaSH濃度を100 fitとし、パルプ濃度を15
Qf/l、浸出時間3Hr、攪拌速度を60ORPMと
したときは、浸出温度30℃の場合は。
The MaSH concentration was set to 100 fit, and the pulp density was set to 15.
Qf/l, leaching time 3Hr, stirring speed 60ORPM, leaching temperature 30°C.

8b67.5%、 Ag 81.3*、 70℃の場合
は、  81) 79.5%。
8b 67.5%, Ag 81.3*, at 70°C: 81) 79.5%.

As 85.0%であυ、その他の金属はほとんど浸出
されず効率の良い選択抽出が可能であった。
The As content was 85.0%, and other metals were hardly leached out, allowing efficient selective extraction.

Na8H濃度を200 g/lとし、パルプ濃度を15
Of/A、浸出時間3Hr、攪拌速度を60ORPMと
したときは、浸出温度30℃の場合は。
The Na8H concentration was 200 g/l and the pulp concentration was 15
Of/A, leaching time 3Hr, stirring speed 60ORPM, leaching temperature 30°C.

8b 89.3チ、 As 92チ、70℃の場合は、
81)95チ。
8b 89.3chi, As 92chi, 70℃,
81) 95chi.

Aθ9A7%であシ、その他の金属はほとんど浸出され
ず、よシ良い選択抽出が可能であった。
The Aθ9A content was 7%, and almost no other metals were leached out, allowing for good selective extraction.

実施例2 銅’Jkflニオケル分銀煙灰(Sb 17.4%、 
As S、29%。
Example 2 Copper'Jkfl nickel silver smoke ash (Sb 17.4%,
As S, 29%.

Bi 15.6%、 Cu 5.21S、 Pb 17
.a先A61.01S、 T、86.44S)を硫化ソ
ーダ液で浸出処理を行った。
Bi 15.6%, Cu 5.21S, Pb 17
.. A (A61.01S, T, 86.44S) was leached with a sodium sulfide solution.

11a、8濃度を100 fitとし、ノ(ルプ濃度を
150f/L 、浸出時間3Hr、攪拌速度を600 
KPMとしたときは、浸出温度30℃の場合は、  8
1)71.5チ。
11a, 8 concentration was 100 fit, No(luple concentration was 150 f/L, leaching time was 3 Hr, stirring speed was 600
When KPM is used, if the leaching temperature is 30℃, 8
1) 71.5ch.

As 7Q、6−、 70℃の場合、  sb 81.
1%、 As 79.7−であり、その他の金属はほと
んど浸出されず効率の良い選択抽出が可能であった。
As 7Q, 6-, at 70°C, sb 81.
1%, As 79.7-, other metals were hardly leached out and efficient selective extraction was possible.

Na、S 濃度を200 t/lとし、ノくルプ濃度を
1509/l、浸出時間5Hr、攪拌速度を60ORP
Mとしたときは、浸出温度30℃の場合は。
Na, S concentration was 200 t/l, Norkulp concentration was 1509/l, leaching time was 5 Hr, stirring speed was 60 ORP.
When M is used, the leaching temperature is 30°C.

Sb 90.2%、 As a&5%、 70℃の場合
は、  sb 96.3%。
Sb 90.2%, Asa&5%, sb 96.3% at 70℃.

As 941%であり、その他の金属はほとんど浸出さ
れず、より良い選択抽出が可能であった。
As content was 941%, other metals were hardly leached out, and better selective extraction was possible.

比較例 実施例1と同様な条件で、硫駿又はカセイソーダで処理
した場合は、  sb及び又はAsが選択的に抽出でき
なかった。
Comparative Example When treated with sulfur or caustic soda under the same conditions as in Example 1, sb and/or As could not be selectively extracted.

Claims (3)

【特許請求の範囲】[Claims] (1)アンチモン及びまたはひ素を含む物質の処理方法
において、水硫化ソーダにより処理することを特徴とす
るアンチモン及び又はひ素の選択浸出方法。
(1) A method for selectively leaching antimony and/or arsenic, the method comprising treating a substance containing antimony and/or arsenic with sodium hydrogen sulfide.
(2)特許請求の範囲第1項において、浸出温度が70
〜90℃であることを特徴とするアンチモン及び又はひ
素の選択浸出方法。
(2) In claim 1, the leaching temperature is 70°C.
A selective leaching method for antimony and/or arsenic, characterized in that the temperature is ~90°C.
(3)特許請求の範囲第1項において、浸出液の水硫化
ソーダ及び又は硫化ソーダの濃度が 150〜250g/lであることを特徴とするアンチモ
ン及び又はひ素の選択浸出方法。
(3) The method for selective leaching of antimony and/or arsenic according to claim 1, characterized in that the concentration of sodium bisulfide and/or sodium sulfide in the leaching solution is 150 to 250 g/l.
JP27213084A 1984-12-25 1984-12-25 Selective leaching of antimony and/or arsenic Pending JPS61151027A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP27213084A JPS61151027A (en) 1984-12-25 1984-12-25 Selective leaching of antimony and/or arsenic

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP27213084A JPS61151027A (en) 1984-12-25 1984-12-25 Selective leaching of antimony and/or arsenic

Publications (1)

Publication Number Publication Date
JPS61151027A true JPS61151027A (en) 1986-07-09

Family

ID=17509506

Family Applications (1)

Application Number Title Priority Date Filing Date
JP27213084A Pending JPS61151027A (en) 1984-12-25 1984-12-25 Selective leaching of antimony and/or arsenic

Country Status (1)

Country Link
JP (1) JPS61151027A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6455342A (en) * 1987-08-26 1989-03-02 Sumitomo Metal Mining Co Method for recovering of valuables
JPH055347U (en) * 1991-07-09 1993-01-26 オークマ株式会社 Machine tool chip removal device
JP2009074129A (en) * 2007-09-20 2009-04-09 Dowa Metals & Mining Co Ltd Method for recovering tin
JP2011161386A (en) * 2010-02-10 2011-08-25 Akita Univ Method for treating thioarsenite
CN107365913A (en) * 2017-06-29 2017-11-21 红河绿地环保科技发展有限公司 Arsenic, the method for antimony high-efficiency comprehensive utilization in a kind of As and Sb flue dust

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4961086A (en) * 1972-09-22 1974-06-13

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4961086A (en) * 1972-09-22 1974-06-13

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6455342A (en) * 1987-08-26 1989-03-02 Sumitomo Metal Mining Co Method for recovering of valuables
JPH055347U (en) * 1991-07-09 1993-01-26 オークマ株式会社 Machine tool chip removal device
JP2009074129A (en) * 2007-09-20 2009-04-09 Dowa Metals & Mining Co Ltd Method for recovering tin
JP2011161386A (en) * 2010-02-10 2011-08-25 Akita Univ Method for treating thioarsenite
CN107365913A (en) * 2017-06-29 2017-11-21 红河绿地环保科技发展有限公司 Arsenic, the method for antimony high-efficiency comprehensive utilization in a kind of As and Sb flue dust
CN107365913B (en) * 2017-06-29 2019-01-29 红河绿地环保科技发展有限公司 A kind of method of arsenic in As and Sb flue dust, antimony high-efficiency comprehensive utilization

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