JPS62161989A - Method for recovering bismuth and/or mercury - Google Patents

Method for recovering bismuth and/or mercury

Info

Publication number
JPS62161989A
JPS62161989A JP60204476A JP20447685A JPS62161989A JP S62161989 A JPS62161989 A JP S62161989A JP 60204476 A JP60204476 A JP 60204476A JP 20447685 A JP20447685 A JP 20447685A JP S62161989 A JPS62161989 A JP S62161989A
Authority
JP
Japan
Prior art keywords
bismuth
mercury
bath
hydrochloric acid
blown
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
Application number
JP60204476A
Other languages
Japanese (ja)
Other versions
JPH033751B2 (en
Inventor
Shuichi Oto
修一 大戸
Naomi Sasahara
笹原 直見
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 JP60204476A priority Critical patent/JPS62161989A/en
Publication of JPS62161989A publication Critical patent/JPS62161989A/en
Publication of JPH033751B2 publication Critical patent/JPH033751B2/ja
Granted legal-status Critical Current

Links

Classifications

    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P10/00Technologies related to metal processing
    • Y02P10/20Recycling

Landscapes

  • Electrolytic Production Of Metals (AREA)

Abstract

PURPOSE:To efficiently recover bismuth and mercury in a hydrochloric acid bath by blowing H2S and H2C2O4 into the bath and carrying out electrolysis. CONSTITUTION:When bismuth and/or mercury in a hydrochloric acid bath is recovered, H2S and/or H2C2O4 is blown into the bath and electrolysis is carried out. At this time, the hydrochloric acid bath is prepd. as a bath acidified with hydrochloric acid to >=about 1N, a carbon electrode or the like is used as the anode and a copper plate as the cathode. H2S and/or H2C2O4 is preferably blown into the bath on the anode side. The amount of H2C2O4 blown is about 1.0-1.7 times the reaction equiv. and H2S is blown to such a degree that the electrolytic soln. is not impregnated with the odor of Cl2. The current density is about 30-250A/dm<2> and the temp. of the electrolytic soln. is ordinary temp. Thus, bismuth and/or mercury can be efficiently recovered.

Description

【発明の詳細な説明】 l匪π1蝮 本発明は、ビスマス及び又は水銀の回収法に関する。[Detailed description of the invention] 1 匪π1 匮 The present invention relates to a method for recovering bismuth and/or mercury.

鴛」乳」L援 従来ビスマス及び又は水銀の回収法で簡易にビスマス、
水銀を液中から回収する方法がなかった。
Bismuth can be easily recovered using conventional bismuth and/or mercury recovery methods.
There was no way to recover mercury from the liquid.

このため1例えば塩酸酸性の液でイオン交換樹脂もしく
はキレ−1−樹脂に吸着した金属を溶離し。
For this purpose, the metals adsorbed on the ion exchange resin or Kire-1 resin are eluted with an acidic solution such as hydrochloric acid.

目的金属を回収する方法においては、溶m液を循環使用
することが好ましいが、好ましい回収方法がなかったた
めこの再循環液中にビスマスが濃縮残存した場合数のよ
うな問題を生じていた。即ち、レニウム、アンチモン等
の回収法において、液中にビスマスが濃縮するとイオン
交換樹脂の吸着性能が劣化し、好ましい回収処理を行う
ことができなくなる。
In the method for recovering the target metal, it is preferable to recycle the solution, but since there was no suitable recovery method, problems have arisen in cases where bismuth remains concentrated in the recycled solution. That is, in a method for recovering rhenium, antimony, etc., if bismuth is concentrated in the liquid, the adsorption performance of the ion exchange resin deteriorates, making it impossible to perform a preferable recovery process.

そこで、ビスマス及び又は水銀を系外に回収する好まし
い方法が要望されていた。
Therefore, there has been a need for a preferable method for recovering bismuth and/or mercury out of the system.

また本発明は、上記の場合のみに限定されることなく、
液中のビスマス及び又は水銀を効率よく回収する方法で
ある。
Furthermore, the present invention is not limited to the above cases, but
This is a method for efficiently recovering bismuth and/or mercury in liquid.

l匪夙監双 即ち、塩酸浴中のビスマス及び又は水銀の回収法におい
て、ビスマス及び又は水銀含有液中に1(2Sおよび又
はH2C,O,を吹き込み、電解を行うビスマス及び又
は水銀の回収法を提供するものである。
A method for recovering bismuth and/or mercury in which 1 (2S and/or H2C, O) is blown into a bismuth and/or mercury-containing solution and electrolysis is carried out. It provides:

見匪立務朋 本発明で対象となる溶液は、塩酸酸性浴(1規定以上)
である。 ビスマス、水銀の濃度は、特に限定を要しな
い。例えば、レニウムをイオン交換樹脂で回収する方法
において、その溶離液を塩酸酸性とし、レニウムを溶離
回収するが、この場合循環使用されると1〜5g#lの
ビスマス、及び0.07〜0.04gIQの水銀が蓄積
される。
The solution targeted by the present invention is a hydrochloric acid acid bath (1N or more).
It is. The concentrations of bismuth and mercury are not particularly limited. For example, in a method of recovering rhenium using an ion exchange resin, the eluent is made acidic with hydrochloric acid, and rhenium is eluted and recovered.In this case, when recycled, 1 to 5 g#l of bismuth and 0.07 to 0.0 g/l are recovered. 04gIQ of mercury accumulates.

このような液を処理する場合は、陽極に例えば不溶性陽
極を用いる。例えば、カーボン電極等である。さらに陰
極には9例えば銅板が用いられる。
When processing such a liquid, an insoluble anode, for example, is used as the anode. For example, it is a carbon electrode. Furthermore, a copper plate, for example, is used as the cathode.

本発明における【12Sおよび又はH,C,O,の添加
は。
The addition of [12S and/or H, C, O,] in the present invention is as follows.

上記陽極側に添加することが好ましい。これは、−電解
により陽極に発生するC12ガスが陽極面で0式の反応
により溶解し、陰極に析出するBiを00式の反応によ
り溶解するためBiの回収率が低下するためであり、 
H2Sおよび11□C2O4等の還元剤を添加すること
により、 HCl0を00式の反応により分解すること
によりBiの回収率が大幅に高められるものと思われる
It is preferable to add it to the anode side. This is because - the C12 gas generated at the anode by electrolysis is dissolved on the anode surface by the 0-type reaction, and the Bi deposited on the cathode is dissolved by the 00-type reaction, resulting in a decrease in the recovery rate of Bi.
It is believed that by adding a reducing agent such as H2S and 11□C2O4, the recovery rate of Bi can be greatly increased by decomposing HCl0 by the 00-type reaction.

C12+8,0→)ICI + HCl0      
・・・・・・■311CIO+ 2Bi −+ Bi、
 O1+ 311C1・・・・・・■Bi、0. + 
611C1→2BiC1,+ 3H,O・・・・・・■
HCl0+11.S−+l+C1+S’ +l+、0 
    ・・・・・・■11cIO+ 11.C2O4
→HCI + 2CO2+H□0・・・・・・■H,S
および又は112c20.の吹き込み量は、 !I、C
20゜については1反応当量の1.0倍〜1.7倍程度
、 H,Sについては、電解液にC12臭が着臭しない
ように吹き込むことが好ましい。
C12+8,0→)ICI+HCl0
・・・・・・■311CIO+ 2Bi −+ Bi,
O1+ 311C1...■Bi, 0. +
611C1→2BiC1,+3H,O・・・・・・■
HCl0+11. S-+l+C1+S' +l+, 0
・・・・・・■11cIO+ 11. C2O4
→HCI + 2CO2+H□0・・・・・・■H,S
and or 112c20. The amount of blowing is ! I,C
For 20°, it is preferable to blow about 1.0 to 1.7 times the amount of one reaction equivalent, and for H and S, it is preferable to blow in so that the C12 odor does not attach to the electrolytic solution.

電解条件は、電流密度が30〜250A/イ、電解液温
度は常温1等の条件であることが好ましい。
The electrolytic conditions are preferably such that the current density is 30 to 250 A/I, and the electrolytic solution temperature is room temperature 1, etc.

発明の効果 以上のように本発明を実施することにより以下の効果を
有する。
Effects of the Invention By implementing the present invention as described above, the following effects can be obtained.

(1)溶液中のビスマス及び又は水銀を効率良く回収で
きる。
(1) Bismuth and/or mercury in the solution can be efficiently recovered.

(2)レニウムの回収工程において循環使用する塩酸酸
性溶離液から、ビスマスや水銀等を効率良く回収できる
(2) Bismuth, mercury, etc. can be efficiently recovered from the hydrochloric acid acidic eluent that is recycled in the rhenium recovery process.

(3)銅電解液のキレート樹脂によるsb等の除去工程
において循環使用する塩酸酸性溶離液から。
(3) From the hydrochloric acid acidic eluent that is recycled in the process of removing sb, etc. using a chelate resin of copper electrolyte.

ビスマス及び又は水銀を効率良く回収できる。Bismuth and/or mercury can be efficiently recovered.

(4)溶離液の有害成分の蓄積がなく繰り返し使用が可
能となる。
(4) The eluent does not accumulate harmful components and can be used repeatedly.

夫五匹上 ビスマスを含む塩酸溶液にH2C,04,H,Sをそれ
ぞれ反応当量の1.5倍添加し、4条件で処理した結果
2表1のごとくビスマスの回収が効率良く行われた。
1.5 times the reaction equivalent of H2C, 04, H, and S were each added to a hydrochloric acid solution containing bismuth and treated under four conditions. As a result, bismuth was efficiently recovered as shown in Table 2.

原液中のビスマスは、3.5〜3.66g/ fiのも
のを供試料として、約22時間後の液中のビスマスは。
The bismuth in the stock solution was 3.5 to 3.66 g/fi as a sample, and the bismuth in the solution after about 22 hours was as follows.

0.93〜0.12g/fiと効率の良い回収ができた
。特にH,Sを添加したものがビスマスの回収率が高い
値を示した。
Efficient recovery of 0.93 to 0.12 g/fi was achieved. In particular, those to which H and S were added showed a high bismuth recovery rate.

また同様に水銀の回収率も高い値を示した。Similarly, the recovery rate of mercury also showed a high value.

以下余白 比較例1 実施例1と同様な条件で、 H,C20,およびH,S
のいずれも添加しない条件で行った結果9表2のごとく
ビスマスの回収率は22時間後であっても悪い値であっ
た。
Margin Comparative Example 1 Below, under the same conditions as Example 1, H, C20, and H, S
As shown in Table 9, the bismuth recovery rate was poor even after 22 hours.

以下余白Margin below

Claims (1)

【特許請求の範囲】[Claims] (1)塩酸浴中のビスマス及び又は水銀の回収法におい
て、ビスマス及び又は水銀の含有液中にH_2Sおよび
又はH_2C_2O_4を吹き込み、電解を行うことを
特徴とするビスマス及び又は水銀の回収法。
(1) A method for recovering bismuth and/or mercury in a hydrochloric acid bath, characterized in that H_2S and/or H_2C_2O_4 is blown into a liquid containing bismuth and/or mercury to perform electrolysis.
JP60204476A 1985-09-18 1985-09-18 Method for recovering bismuth and/or mercury Granted JPS62161989A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60204476A JPS62161989A (en) 1985-09-18 1985-09-18 Method for recovering bismuth and/or mercury

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60204476A JPS62161989A (en) 1985-09-18 1985-09-18 Method for recovering bismuth and/or mercury

Publications (2)

Publication Number Publication Date
JPS62161989A true JPS62161989A (en) 1987-07-17
JPH033751B2 JPH033751B2 (en) 1991-01-21

Family

ID=16491157

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60204476A Granted JPS62161989A (en) 1985-09-18 1985-09-18 Method for recovering bismuth and/or mercury

Country Status (1)

Country Link
JP (1) JPS62161989A (en)

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS52128804A (en) * 1976-04-22 1977-10-28 Stanley Electric Co Ltd Electrolytic recovery of metal

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS52128804A (en) * 1976-04-22 1977-10-28 Stanley Electric Co Ltd Electrolytic recovery of metal

Also Published As

Publication number Publication date
JPH033751B2 (en) 1991-01-21

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