JPH0510437B2 - - Google Patents
Info
- Publication number
- JPH0510437B2 JPH0510437B2 JP26279586A JP26279586A JPH0510437B2 JP H0510437 B2 JPH0510437 B2 JP H0510437B2 JP 26279586 A JP26279586 A JP 26279586A JP 26279586 A JP26279586 A JP 26279586A JP H0510437 B2 JPH0510437 B2 JP H0510437B2
- Authority
- JP
- Japan
- Prior art keywords
- conductor
- liquid
- deposits
- electrode
- electrolytic cell
- 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.)
- Expired - Lifetime
Links
Landscapes
- Electrolytic Production Of Metals (AREA)
- Conductive Materials (AREA)
Description
<産業上の利用分野>
本発明は金属塩電解槽の電極に通電するために
電解槽に設置すべき導電体の改良に関する。
<従来の技術>
一般に金属塩水溶液の電解においては、電解槽
側壁上に設置された導電体と該導電体に接触して
いる陽・陰極との各接点の接触抵抗を小さく且つ
バラツキを少くするために種々の工夫がなされて
いる。例えば、特公昭49−16686号公報には上記
接点部を導電性の液体で湿潤状態に保つことによ
り長時間の電解を行つても接触抵抗が小さく且つ
そのバラツキを少くした導電体が開示されてい
る。この導電体は銅電解精製における例である第
1図及び第2図に示すように、導電体本体1に含
液部2を設けてこの含液部2の内部に海綿などの
含浸性海綿物体3を置き、この含浸性海綿物体3
を介して電極又は電極ビーム4(クロスバーまた
はシヨルダー)を支持するようにし、含液部2に
は導電性液体を連続的に滴下、又は継続的に補給
して海綿物体3が電極4との接触部において常に
含水状態に保たれるようにしたものである。そし
て、導電性液体としては水道水、工業用水(地下
水等)などを用いていた。
<発明が解決しようとする問題点>
しかしながら、上述したような従来の導電体に
おいては付着物が発生するが、この付着物は通常
酸化被膜の洗浄のために行う希硫酸の散布ではと
れないという問題があつた。よつて、上記導電体
では導電性液体を含浸する含浸性海綿物体3が劣
化した場合の取替の他、導電体に発生する付着物
の研磨法が必要であつた。
本発明はこのような事情に鑑み、付着物の発生
を防止した金属塩電解槽の導電体を提供すること
を目的とする。
<問題点を解決するための手段>
本発明者らは上記問題点を解決するために種々
検討を重ねた結果、導電体内に発生する付着物の
主成分は硫酸カルシウムであり、この硫酸カルシ
ウムは導電体の通電による抵抗熱のために揮発さ
れて濃縮された導電性液体中のCaと、飛散した
電解液中の硫酸又は洗浄に用いた希硫酸で水洗浄
後残留したものとが反応したものであることを知
見した。
かかる知見に基づく本発明の構成は、導電性液
体を介して電極又は電極ビームと接触するように
形成されるとともに、電解液として金属硫酸塩を
用いる金属電解槽に使用されるか又は洗浄液とし
て硫酸を含有する液を用いる金属塩電解槽の導電
体において、該導電体内に供給する導電性液体の
カルシウム濃度が1mg/以下であることを特徴
とする。
<実施例>
以下に実施例を示し、本発明をさらに詳細に説
明する。
第1図及び第2図に示す導電体と同様なものを
銅電解工場の銅電解槽に設置し、これに水道水を
軟化装置(オルガノ製SAT−256)に通して軟化
した水を導電製液体として供給した。このときの
軟化した水Ca含有量は1mg/以下である。
本実施例においては定期的な希硫酸による酸洗
後、水洗することにより長期に亘つて安定した操
業ができ、付着物の研磨除去は年の1回行えば十
分であつた。この除去した付着物の平均組成を表
−1に示す。
なお、同様の装置で水道水をそのまま導電性液
体とした比較例では3ケ月に1回の割合では付着
物の研磨除去が必要であつた。このときの供給し
た水道水のCa含有量は19mg/であり、また付
着物の組成は表−1に示す通りであつた。
<Industrial Application Field> The present invention relates to an improvement in a conductor to be installed in an electrolytic cell in order to supply electricity to the electrodes of the metal salt electrolytic cell. <Prior art> In general, in the electrolysis of metal salt aqueous solutions, the contact resistance of each contact point between a conductor installed on the side wall of an electrolytic cell and an anode/cathode in contact with the conductor is reduced and variation is reduced. Various efforts have been made for this purpose. For example, Japanese Patent Publication No. 49-16686 discloses a conductor that has a low contact resistance and less variation even during long-term electrolysis by keeping the contact portion wet with a conductive liquid. There is. As shown in FIGS. 1 and 2, which are examples of copper electrolytic refining, this conductor has a liquid-impregnated part 2 in a conductor main body 1, and an impregnable sponge material such as a sponge inside the liquid-impregnated part 2. 3, and this impregnable sponge object 3
The electrode or the electrode beam 4 (crossbar or shoulder) is supported through the liquid-containing part 2, and conductive liquid is continuously dropped or replenished to the liquid-containing part 2 so that the sponge object 3 is connected to the electrode 4. The contact area is always kept hydrated. Tap water, industrial water (groundwater, etc.), etc., have been used as the conductive liquid. <Problems to be Solved by the Invention> However, in the conventional conductor as described above, deposits are generated, and it is said that this deposit cannot be removed by spraying dilute sulfuric acid, which is normally used to clean the oxide film. There was a problem. Therefore, in the above conductor, in addition to replacing the impregnated sponge body 3 impregnated with the conductive liquid when it deteriorates, it is necessary to polish the deposits generated on the conductor. In view of these circumstances, an object of the present invention is to provide a conductor for a metal salt electrolytic cell that prevents the generation of deposits. <Means for Solving the Problems> As a result of various studies conducted by the present inventors in order to solve the above problems, the main component of the deposits generated inside the conductor is calcium sulfate, and this calcium sulfate is A reaction between Ca in the conductive liquid, which was volatilized and concentrated due to the resistance heat generated by the conductor's energization, and the sulfuric acid in the scattered electrolyte or the dilute sulfuric acid used for cleaning that remained after washing with water. We found that. The configuration of the present invention based on such knowledge is formed so as to be in contact with an electrode or an electrode beam via a conductive liquid, and is used in a metal electrolytic cell that uses a metal sulfate as an electrolyte or sulfuric acid as a cleaning liquid. A conductor for a metal salt electrolytic cell using a liquid containing a metal salt electrolytic cell is characterized in that the conductive liquid supplied into the conductor has a calcium concentration of 1 mg/min or less. <Example> The present invention will be explained in further detail by showing examples below. A conductor similar to the one shown in Figures 1 and 2 was installed in a copper electrolytic tank at a copper electrolysis factory, and tap water was passed through a softening device (SAT-256 manufactured by Organo) and the softened water was used to make conductors. Supplied as a liquid. The Ca content of the softened water at this time is 1 mg/or less. In this example, periodic pickling with dilute sulfuric acid followed by water rinsing enabled stable operation over a long period of time, and it was sufficient to remove deposits by polishing once a year. Table 1 shows the average composition of the removed deposits. In addition, in a comparative example in which tap water was used as a conductive liquid using a similar device, it was necessary to polish and remove deposits once every three months. The Ca content of the supplied tap water at this time was 19 mg/, and the composition of the deposits was as shown in Table 1.
【表】
表−1から本実施例において発生した多少の付
着物は硫酸銅が主成分であると予想でき、希硫酸
で洗浄可能であることと一致する。
上記実施例においては付着物低下により接触抵
抗が低減されており、比較例に比べて3mV低下
された。これにより、電気銅生産の原単位を
3kwH/T減ずることができた。
このように、導電体内に供給する導電性液体中
のCa含有量を1mg/以下、好ましくは0.1mg/
以下とすれば付着物が大きく低減できる。な
お、上記実施例として水以外の液体とする場合
も、母液と使用する水を上述と同様に軟化した水
とするようにすればよい。
<発明の効果>
以上、実施例とともに具体的に説明したよう
に、本発明にかかる導電体を用いれば、付着物の
発生が少なくなり、また発生する付着物を洗浄す
る希硫酸に溶けやすい硫酸銅となるので、付着物
の研磨除去の作業の回数を大幅に減ずることがで
きる。これにより、導電体と電極との接触抵抗が
小さくなり、またそのバラツキも小さくなる。[Table] From Table 1, it can be predicted that the main component of some of the deposits generated in this example was copper sulfate, which is consistent with the fact that it can be cleaned with dilute sulfuric acid. In the above example, the contact resistance was reduced due to the reduction in deposits, and was reduced by 3 mV compared to the comparative example. This will reduce the basic unit of electrolytic copper production.
We were able to reduce the power by 3kwH/T. In this way, the Ca content in the conductive liquid supplied into the conductor is set to 1 mg/or less, preferably 0.1 mg/
If the amount is set below, the amount of deposits can be greatly reduced. Note that even when using a liquid other than water in the above embodiment, the water used as the mother liquor may be softened water in the same manner as described above. <Effects of the Invention> As specifically explained above in conjunction with the examples, the use of the conductor according to the present invention reduces the generation of deposits, and the sulfuric acid that is easily soluble in dilute sulfuric acid used to clean the deposits that are generated. Since the material is made of copper, the number of polishing operations required to remove deposits can be significantly reduced. This reduces the contact resistance between the conductor and the electrode, and also reduces its variation.
第1図は導電性液体を介して電極又は電極ビー
ムと接触する導電体を示す説明図、第2図はその
断面図である。
図面中、1は導電体本体、2は含液部、3は含
浸性海綿体、4は電極又は電極ビームである。
FIG. 1 is an explanatory view showing a conductor in contact with an electrode or an electrode beam via a conductive liquid, and FIG. 2 is a cross-sectional view thereof. In the drawings, 1 is a conductor main body, 2 is a liquid-containing part, 3 is an impregnated corpus cavernosum, and 4 is an electrode or an electrode beam.
Claims (1)
触するように形成されるとともに、電解液として
金属硫酸塩を用いる金属電解槽に使用されるか又
は洗浄液として硫酸を含有する液を用いる金属塩
電解槽の導電体において、該導電体内に供給する
導電性液体のカルシウム濃度が1mg/以下であ
ることを特徴とする金属塩電解槽の導電体。1 Metal salt electrolysis formed in contact with the electrode or electrode beam via a conductive liquid and used in a metal electrolytic cell using a metal sulfate as the electrolyte or using a liquid containing sulfuric acid as the cleaning liquid 1. A conductor for a metal salt electrolytic cell, characterized in that a conductive liquid supplied into the conductor has a calcium concentration of 1 mg/min or less.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP26279586A JPS63118091A (en) | 1986-11-06 | 1986-11-06 | Electric conductor for electrolytic cell containing metallic salt |
| AU80842/87A AU595949B2 (en) | 1986-11-06 | 1987-11-05 | Electric conductor for metal salt electrolytic cell |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP26279586A JPS63118091A (en) | 1986-11-06 | 1986-11-06 | Electric conductor for electrolytic cell containing metallic salt |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS63118091A JPS63118091A (en) | 1988-05-23 |
| JPH0510437B2 true JPH0510437B2 (en) | 1993-02-09 |
Family
ID=17380710
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP26279586A Granted JPS63118091A (en) | 1986-11-06 | 1986-11-06 | Electric conductor for electrolytic cell containing metallic salt |
Country Status (2)
| Country | Link |
|---|---|
| JP (1) | JPS63118091A (en) |
| AU (1) | AU595949B2 (en) |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4916686B1 (en) * | 1970-05-07 | 1974-04-24 | ||
| JPS4916686A (en) * | 1972-06-09 | 1974-02-14 |
-
1986
- 1986-11-06 JP JP26279586A patent/JPS63118091A/en active Granted
-
1987
- 1987-11-05 AU AU80842/87A patent/AU595949B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| AU595949B2 (en) | 1990-04-12 |
| JPS63118091A (en) | 1988-05-23 |
| AU8084287A (en) | 1988-05-12 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EXPY | Cancellation because of completion of term |