JPS5959891A - Anode for electrowinning metal - Google Patents

Anode for electrowinning metal

Info

Publication number
JPS5959891A
JPS5959891A JP16762182A JP16762182A JPS5959891A JP S5959891 A JPS5959891 A JP S5959891A JP 16762182 A JP16762182 A JP 16762182A JP 16762182 A JP16762182 A JP 16762182A JP S5959891 A JPS5959891 A JP S5959891A
Authority
JP
Japan
Prior art keywords
anode
metal
alloy
potential
lead
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
JP16762182A
Other languages
Japanese (ja)
Inventor
Jiro Kurihara
栗原 二郎
Kazuo Koike
一男 小池
Fujio Sawaguchi
澤口 藤雄
Chihiro Hayashi
林 千広
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.)
Akita Seiren KK
Original Assignee
Akita Seiren KK
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 Akita Seiren KK filed Critical Akita Seiren KK
Priority to JP16762182A priority Critical patent/JPS5959891A/en
Publication of JPS5959891A publication Critical patent/JPS5959891A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To enable a drop in anode potential while reducing the amount of Ag, by adding a specified amount of Ca to a Pb-Ag alloy. CONSTITUTION:This anode for electrowinning metal is made of an alloy having a composition consisting of 0.2-2.0wt% Ca, 0.2-1.2wt% Ag and the balance Pb with inevitable impurities. By the composition the contamination of Zn or other metal deposited on a cathode with Pb can be reduced, and the anode potential can be dropped while reducing the amount of Ag. The anode is used to electrowinning metal in an acidic aqueous soln. of sulfuric acid.

Description

【発明の詳細な説明】 本発明に、例えば硫酸酸性水溶液の金属′dL解採取用
に使用し1こ場合に、特に陽極電位全低下さ仕ることが
できる不溶性陽極に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an insoluble anode which can be used, for example, for dissolving metal 'dL in an aqueous sulfuric acid solution, and in this case can in particular be used to reduce the total anode potential.

陰極iff!lに目的金属全析出させる水溶液系の金属
電解採取において、その不溶性陽極としてVJその素拐
C鉛を使用するのが最も−・般的である。し、力)し、
鉛単体の陽極の場合は鉛の溶出や表面に生成し1こpb
o、、の脱落によって析出金属のpb汚染が1川題とな
る。この7こめ、従来より各種の鉛合金からなる陽極の
使用が試みられている。例えば、Ag全添加し1ζもの
などである。
Cathode if! In aqueous metal electrowinning in which the target metal is completely precipitated on a metal, it is most common to use VJ and ground carbon lead as the insoluble anode. , power),
In the case of an anode made of lead alone, lead elutes and forms on the surface, resulting in 1 ppb.
PB contamination of the precipitated metal becomes a major problem due to the falling off of the metal. For this reason, attempts have been made to use anodes made of various lead alloys. For example, it is 1ζ with all Ag added.

しかし、これ徒での鉛合金不溶性陽極は陽極電位が高く
、溶出抵抗や銅酸化性と共に低陽極電位性を兼備し1こ
陽極の開発が強く望1れてい1こ。
However, the lead alloy insoluble anode has a high anode potential, and has a low anodic potential as well as elution resistance and copper oxidation property, and the development of this anode is strongly desired.

本発明はこの要求を満1こす不溶性陽極の提供金目白り
としてなされ1こもので、この目的VCおいてf小々の
試験研究ケ重ね77C結果、C!a 全0.2〜2.0
重片1幅、クイ4しくに1.U〜20屯111φ、およ
び八[を0.2〜1.2重量係の計てI”blc複合添
加して陽極に構成すると、陰極に析出する金属へのPb
汚染を低くしながら陽極電位を低くできることがわがつ
1こ。
The present invention was made with the aim of providing an insoluble anode that satisfies this requirement, and as a result of a series of small tests and research conducted in VC for this purpose, C! a Total 0.2-2.0
1 width of heavy piece, 1 piece of 4 pieces. When U ~ 20 tons 111φ and 8 [0.2 to 1.2 weight coefficient I"blc are added in a composite manner to form the anode, Pb will be added to the metal precipitated on the cathode.
One advantage is that the anode potential can be lowered while reducing contamination.

本発明の不溶性陽極は、P 11)−へg系にCa全0
.2〜2.011を潰裂、好ま(〜くは1.0〜2.0
重量製添加し1ζ点に大きなtiケ徴があるが、この昂
のCa全添加−1−ると、PPb−7N系の場合よりも
陽極電位を丁けることができ、(−力)も、この場合(
’j 、  Y’■、+ −Afl系のΔR量全全減少
ぜても陽極電位の低下効果は大きくは変らないことがわ
かつ1こ。し1こがって、従来試みられたPI)−Ag
系陽極よりもAg量全滅少さピ“ながら先述の目的が達
成でき、高価なAg使用量ケ低減できる−しても経済的
に有利な而をもっている。
The insoluble anode of the present invention has a total of 0 Ca in the P11)-heg system.
.. 2 to 2.011, preferably 1.0 to 2.0
Although there is a large ti characteristic at the 1ζ point when the weight is added, when the total Ca addition is -1-, the anodic potential can be lowered than in the case of the PPb-7N system, and the (-force) is also in this case(
It was found that even if the amount of ΔR in the 'j, Y'■, + -Afl system was completely reduced, the effect of lowering the anode potential did not change significantly. Therefore, the previously attempted PI)-Ag
The above-mentioned objective can be achieved while reducing the total amount of Ag used compared to the system anode, and the amount of expensive Ag used can be reduced, which is economically advantageous.

1匂極ニ構成−4−ろl/cvs、Ca−Pb1合金、
Ag −Pb1り合金および純鉛ケ、Ca ; 0.2
〜2.0市量係、Δg;02〜12屯量係となるようl
lc調年し、黒鉛/l・ツボに入れて電気炉中で溶解攪
拌1〜、これ全陽極形状の鋼製鋳型VCrE:、入して
自然放玲丁ればよい。
1 Aroma electrode composition - 4-l/cvs, Ca-Pb1 alloy,
Ag-Pb1 alloy and pure lead, Ca; 0.2
~2.0 market volume ratio, Δg; 02~12 tonne volume ratio l
LC adjustment, put it in a graphite/L pot, melt and stir in an electric furnace, then put it into a steel mold VCrE with an all-anode shape and let it cool naturally.

そして、得られ1こ陽極を、歪除去の7こめに、180
〜190Cで例えば2昼夜程度(48時間)の焼鈍処f
、!f!到1丁とよい。
Then, after strain removal, the obtained one anode was heated to 180
Annealing treatment at ~190C for about 2 days and nights (48 hours) f
,! f! One piece is good.

本発明は陽極を構成する鉛合金中のCaお裏びAg含有
量を先述のように定め1ζ理由は、先πもそ−の装部に
ついて触れ1ζが、これ金(載脱−1−ると、Ca成分
が、0.2チ未満でば陽極電位の低1;゛に効果が現わ
れなく、2.0チを越えると11イ目佼i11!2+”
を水溶液の陽極として使用し7こ場合に石膏が析出して
通電時の導電性の悪化や鉛脱落現象が現われるので好ま
しくなく、まブこ、Δgg分1ついては、0.21未満
では析出金属へのpb汚染の防止効果が十分1)if:
′f!いと共r陽陰′屯位低下効果も小さく、一方、L
2 %を越えて含有させても陽極電位低下の効果の割合
は変らないのでAg使使用打面節減意味力)らも不経済
とな几だけであるという理由に基づく。
In the present invention, the Ca and Ag contents in the lead alloy constituting the anode are determined as described above. If the Ca content is less than 0.2 cm, no effect will appear on the low anode potential, and if it exceeds 2.0 cm, the 11th point will be 11!2+.
When used as an anode in an aqueous solution, it is not preferable because gypsum will precipitate, resulting in deterioration of conductivity when electricity is applied and a phenomenon of lead falling off. 1) If:
'f! The effect of lowering the r yang yin′ position is also small, while L
This is based on the reason that even if the content exceeds 2%, the effect of lowering the anode potential does not change, so the use of Ag is also uneconomical.

以下に代表的実施例を挙けて本発明陽極の効果全具体的
に示″l−6 実施例1 第1表に示す組成(市11係)の陽橙11本全作成し7
こ。各陽杉の寸法は、液浸漬部において、50mm (
縦)x30+++m(横)x5mm(厚さ)である。
The effects of the anode of the present invention will be specifically illustrated below by giving representative examples.
child. The dimensions of each Yangsugi are 50mm (
Length) x 30+++ m (width) x 5 mm (thickness).

各陽極げ電解処理に供する前に反応表面全化成処理して
おい1屯。
Before each anode is subjected to electrolytic treatment, the entire reaction surface is chemically treated.

電10子試験にさいしては、19易捧1枚に対して純ア
ルミニワム板力・らなる陰極2枚い」法に陽極と同1−
)倉容積500 ccの電解槽に、極間距離を陽極陰極
の面間で30mmとしてセットすると共に、亜鉛濃度6
4fl、/1.遊離硫酸156?/lからなる硫j* 
dIv鉛水溶nり’k ′[!:解液とし、′電流密度
45 mA /li、’+1.+9Ii′液1=31c
で24時間電電解し、7tC0各試験における浴電圧(
V)、み〃・けの1くり極過電圧(V)お工び陰・陽に
析出シフ1こ亜鉛中の鉛濃度(ppm )をd1測し、
その結果を・第1表に並記しノζ。
For the electric 10-electrode test, two cathodes made of pure aluminum wafer are used for one piece of 19.
) An electrolytic cell with a tank volume of 500 cc was set with an electrode distance of 30 mm between the anode and cathode surfaces, and a zinc concentration of 6.
4fl, /1. Free sulfuric acid 156? /l sulfur j *
dIv lead water soluble nri'k '[! : As a solution, 'current density 45 mA/li, '+1. +9Ii' liquid 1=31c
The bath voltage (
V), the lead concentration (ppm) in the Schiff 1 zinc deposited in the yin and yang of the yin and yang is measured d1,
The results are listed in Table 1.

第1表の結果から明らかなように、本発明の陽極は対照
例および比較例に比していづれも陽極電位が低い。七し
2てNα5とN(16〜8.11との比較刀1ら明らか
なように、Ag含有量が低くでも陽j色電位が低トして
いる。ま)こ、析出lIl!鉛中の1゛1)汚染も良Q
l場合が多い。
As is clear from the results in Table 1, the anode potential of the anode of the present invention is lower than that of the control example and the comparative example. As is clear from the comparison between Nα5 and N(16-8.11), the positive color potential is low even when the Ag content is low. 1゛1) Contamination in lead is also good Q
There are many cases.

実施例 へg;υ、92チ、残部がpbの陽画と、Ag、 、’
 U、ε36係、Ca ; t、96 %、残部13が
円)カらlる陽1* (’J’法はいづれも、浸漬部て
′1υυrrtrn (縦)xso、vl、v+(i黄
ンx 9 mm (厚σンてあ6)2枚と、この陽極と
同寸法の純亜鉛陰極を由いて、容址3000 ccの電
解槽で6、亜m a e 65 fi’/l 、遊離硫
(:fl 179 ’;I/1.(DfII 酸亜鉛水
溶液ケ電解液とし、・険間距離金陽イ傘陰(夕の面間て
26.5 mm、′電流密度48mA/c7、電1す’
1rffmr 43 Uて、24時間′屯11イを20
回繰返し実施し/ζ、、この電解にお(tjる・陰間電
圧の1経時変化金各陽伶VCついて測定し、その結果を
第1図にプロアt・(,7,:。
To the example, g;
U, ε36, Ca; t, 96%, remaining 13 is a circle) 1* x 9 mm (thickness: 6) and a pure zinc cathode of the same size as the anode, in an electrolytic tank with a capacity of 3000 cc, 65 m ae 65 fi'/l, free sulfur (: fl 179'; I/1. (DfII zinc oxide aqueous solution electrolyte, distance between metal and yang 26.5 mm, 'current density 48 mA/c7, electric current density 1/1. '
1 rffmr 43 U, 24 hours' 11 I to 20
This electrolysis was carried out repeatedly /ζ, and the change in negative voltage over time was measured for each positive voltage VC, and the results are shown in Figure 1.

、41図の結果から明らかなように、1〕l)−・Ag
系のものに比べ、本発明のPb −Ag −Ca系の1
湯極は庫間市”2圧がいづれの回数1おいても低い。こ
の差(/:工電解条件が同一であるの一テ二陽極電位に
起因するものである。この傾向は長時間経過後も変わら
ない点が特に注目される。
, As is clear from the results in Figure 41, 1]l)-・Ag
Compared to the Pb-Ag-Ca system of the present invention, the Pb-Ag-Ca system of the present invention
The hot water electrode has a low pressure at all times. This difference (/: is due to the two anode potentials under the same electrolytic conditions. This tendency continues over a long period of time. What is particularly noteworthy is that it remains unchanged.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は、本発明陽極と比較例陽極金回−’jli l
lI’l’条件に供(,1ζ場合の陰間電圧の経時斐化
ケ示す図である。 出願人 秋l1fl製錬株式会宅1
Figure 1 shows the anode of the present invention and the anode of a comparative example.
This is a diagram showing the change in negative voltage over time when subjected to lI'l' conditions.

Claims (1)

【特許請求の範囲】[Claims] 水溶液中の金属全電解採取″′J−るlこめの不溶性陽
極であって、この陽極全構成する金属が[J、2〜2.
0重量係のCaと、02〜1.2重量係のAgと、残部
がPbおよび製造上不d丁避的に混入−」−る不純物元
素と、からなる合金である金属全解採取用陽(仇。
This is an insoluble anode containing all metals in an aqueous solution by electrolytic extraction.
An alloy for total metal extraction that is composed of Ca with a weight ratio of 0, Ag with a weight ratio of 02 to 1.2, and the balance being Pb and impurity elements unavoidably mixed in during manufacturing. (Enemy.
JP16762182A 1982-09-28 1982-09-28 Anode for electrowinning metal Pending JPS5959891A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP16762182A JPS5959891A (en) 1982-09-28 1982-09-28 Anode for electrowinning metal

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP16762182A JPS5959891A (en) 1982-09-28 1982-09-28 Anode for electrowinning metal

Publications (1)

Publication Number Publication Date
JPS5959891A true JPS5959891A (en) 1984-04-05

Family

ID=15853178

Family Applications (1)

Application Number Title Priority Date Filing Date
JP16762182A Pending JPS5959891A (en) 1982-09-28 1982-09-28 Anode for electrowinning metal

Country Status (1)

Country Link
JP (1) JPS5959891A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000042241A1 (en) * 1999-01-13 2000-07-20 Rsr Technologies, Inc. Electrowinning anodes which rapidly produce a protective oxide coating

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS52148420A (en) * 1976-06-04 1977-12-09 Furukawa Electric Co Ltd:The Electrolysis of metal
JPS56127743A (en) * 1980-02-15 1981-10-06 Ruuruutsuinku Gmbh Anode alloy and use thereof

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS52148420A (en) * 1976-06-04 1977-12-09 Furukawa Electric Co Ltd:The Electrolysis of metal
JPS56127743A (en) * 1980-02-15 1981-10-06 Ruuruutsuinku Gmbh Anode alloy and use thereof

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000042241A1 (en) * 1999-01-13 2000-07-20 Rsr Technologies, Inc. Electrowinning anodes which rapidly produce a protective oxide coating

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