JPH06192866A - Production of potassium dicyanoaurate - Google Patents

Production of potassium dicyanoaurate

Info

Publication number
JPH06192866A
JPH06192866A JP4346827A JP34682792A JPH06192866A JP H06192866 A JPH06192866 A JP H06192866A JP 4346827 A JP4346827 A JP 4346827A JP 34682792 A JP34682792 A JP 34682792A JP H06192866 A JPH06192866 A JP H06192866A
Authority
JP
Japan
Prior art keywords
anode
gold
surface area
potassium
current
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
JP4346827A
Other languages
Japanese (ja)
Other versions
JP3202375B2 (en
Inventor
Yoshio Ishikawa
芳夫 石川
Satoru Tsuruoka
哲 鶴岡
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.)
Tokuriki Honten Co Ltd
Original Assignee
Tokuriki Honten 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 Tokuriki Honten Co Ltd filed Critical Tokuriki Honten Co Ltd
Priority to JP34682792A priority Critical patent/JP3202375B2/en
Publication of JPH06192866A publication Critical patent/JPH06192866A/en
Application granted granted Critical
Publication of JP3202375B2 publication Critical patent/JP3202375B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Electrodes For Compound Or Non-Metal Manufacture (AREA)
  • Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)

Abstract

PURPOSE:To improve dissolution efficiency by using a granular gold bullion put in a titanium vessel as the anode and setting a cathode plate through a diaphragm in an electrolytic cell of a potassium cyanide soln. CONSTITUTION:When potassium dicyanoaurate is produced, a granular gold bullion is placed in a titanium vessel and set as an anode in the electrolytic cell of a potassium cyanide soln., and a cathode plate is set through a diaphragm. Consequently, the surface area of the anode is increased, the time until the passivation potential is reached is prolonged because the surface area is not decreased due to dissolution, continuous operation is attained only by adding and replenishing granular gold, the conventional work for attachment and detachment of gold are not needed, and the dissolution efficiency is improved.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、各種金メッキや金合金
メッキの金供給用の薬剤として用いるジシアノ金酸カリ
ウムの製造方法に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for producing potassium dicyanoaurate used as a chemical for supplying gold for various gold plating and gold alloy plating.

【0002】[0002]

【従来の技術】ジシアノ金酸カリウムは、従来より電解
法によって製造されている。この方法は、金地金を板状
の陽極とし、イオン交換樹脂やセラミック等による隔膜
を介して不溶性金属を陰極として対向させ、シアン化カ
リウム溶液中で電解することにより製造するものであ
る。
2. Description of the Related Art Potassium dicyanoaurate has been conventionally produced by an electrolytic method. In this method, a metal plate is used as a plate-shaped anode, an insoluble metal is made to face as a cathode through a diaphragm made of an ion exchange resin or ceramic, and electrolysis is performed in a potassium cyanide solution.

【0003】この方法によると、通電する電流は、陽極
板の表面積に対する電流の大きさ、つまり電流密度をも
とに決定されるもので、この電流密度を維持することに
より金の陽極溶解反応が進行し、保持されるものであ
る。そこで、電解が進み、陽極板の表面積が減少して陽
極表面が不働態化されると、電流値が下がり、酸素ガス
の発生が始まることになる。
According to this method, the current to be applied is determined based on the magnitude of the current with respect to the surface area of the anode plate, that is, the current density, and by maintaining this current density, the anodic dissolution reaction of gold is carried out. It is something that progresses and is retained. Therefore, when the electrolysis progresses and the surface area of the anode plate is reduced to passivate the anode surface, the current value is reduced and the generation of oxygen gas is started.

【0004】そこで、この陽極溶解反応を確保するため
に一定電流を保持しようと電圧をあげると、電流値もあ
がるが、通電した電流は酸素の発生反応に消費されてし
まう。その結果、板状の陽極を使用した場合は、その電
極の全量を溶解することができず、およそ60〜65% の溶
解率となっているのが現状である。
Therefore, if the voltage is increased to maintain a constant current in order to secure the anodic dissolution reaction, the current value increases, but the supplied current is consumed in the oxygen generation reaction. As a result, when a plate-shaped anode is used, the entire amount of the electrode cannot be dissolved, and the current dissolution rate is about 60 to 65%.

【0005】[0005]

【発明が解決しようとする課題】そこで、シアン化カリ
ウムを電解液とし、金板を陽極としたときの電流・電圧
曲線は実験の結果を図1に示すと、電圧を徐々に増すと
電流も増し、a点に達するまで増加して金はシアン化カ
リウムに溶解する。さらに電圧を増すと電流が下がって
b点に達し、その後は電圧を上げると電流も増すが酸素
の発生が激しくなるものの金は溶解しないことになる。
Therefore, the current-voltage curve when potassium cyanide is used as the electrolytic solution and the gold plate is used as the anode is shown in the experimental results in FIG. 1, and the current increases as the voltage gradually increases, Gold dissolves in potassium cyanide increasing until point a is reached. When the voltage is further increased, the current decreases and reaches point b. Then, when the voltage is increased, the current also increases, but the generation of oxygen becomes more intense, but gold is not dissolved.

【0006】また、陽極の表面積を変えたときの電流・
電圧曲線は、図2に示す如く、電流値は、同一電位にお
いては、表面積が大きいものほど電流値も大であること
がわかる。そこで、電解法によるジシアノ金酸カリウム
の製造においは、定電流装置を用いて常に一定電流を保
ち、溶解により表面積が小さくなると電圧をあげて電流
値を保つ働きをするようにしてある。そのため、表面積
の小さい電極は、大きい電極に比べて不働態化電位に達
し易くなり、溶解反応が止まり易くなるという問題があ
る。
In addition, the current when changing the surface area of the anode
As shown in FIG. 2, the voltage curve shows that the current value is larger as the surface area is larger at the same potential. Therefore, in the production of potassium dicyanoaurate by the electrolysis method, a constant current device is used to constantly maintain a constant current, and when the surface area becomes small due to dissolution, the voltage is increased to maintain the current value. Therefore, an electrode with a small surface area is more likely to reach the passivation potential than an electrode with a large surface area, and there is a problem that the dissolution reaction is likely to stop.

【0007】本発明は、陽極の表面積を大きくとり、溶
解による表面積の減少を原因とする不働態化電位までの
到達時間を長くして溶解効率を向上させることを目的と
する。
It is an object of the present invention to increase the surface area of the anode and to improve the dissolution efficiency by lengthening the time required to reach the passivation potential due to the reduction of the surface area due to dissolution.

【0008】[0008]

【課題を解決するための手段】そこで、本発明は、粒状
に加工した金地金をチタン製容器に入れ、シアン化カリ
ウム溶液の電解槽中に陽極としてセットし、陰極板を隔
膜を介してセットしたことを特徴とする。なお、上記容
器の形状は皿状、椀状等どのような形状でもよく溶液の
通過性のよい網体や穴あき容器でもよい。
Therefore, according to the present invention, a granular metal ingot is placed in a titanium container, set as an anode in an electrolytic cell of a potassium cyanide solution, and a cathode plate is set via a diaphragm. Is characterized by. The container may have any shape such as a dish or a bowl, and may be a mesh or a perforated container having a high solution passing property.

【0009】また、陰極板としては、金に限らず、チタ
ン、ステンレス等どのような材料でも可能である。この
ようにすることにより、金の投入量を低く抑え、しかも
表面積を大きくすることができ、材料管理にすぐれると
共に溶解効率を向上させることになり、金の溶解率を約
20% あげることができた。
The cathode plate is not limited to gold, but may be any material such as titanium or stainless steel. By doing so, the amount of gold input can be kept low and the surface area can be increased, which improves the material management and improves the dissolution efficiency.
I was able to raise 20%.

【0010】なお、粒状加工の方法は、溶融した金地金
を水中に投ずることにより処理することができる。
The granular processing method can be performed by pouring molten metal into water.

【0011】[0011]

【実施例】金地金21.5Kgを黒鉛坩堝中で加熱溶解し、溶
湯を水中に少しずつ投入して粒状金を製造する。これ
を、チタンバスケット(150 ×300 ×25mm)4個に均等
に入れてこれを陽極とする。
[Examples] 21.5 Kg of bare metal is melted by heating in a graphite crucible, and the molten metal is gradually poured into water to produce granular gold. This is evenly placed in four titanium baskets (150 × 300 × 25 mm) to form an anode.

【0012】陰極としては、金板(150 ×300 ×1mm )
2枚を作り、素焼隔膜を介して20%シアン化カリウム溶
液中で、60℃、160Aで18時間電解した。その結果、18.6
Kgが溶解し、溶解率は86.5% であった。この溶液を一般
的な濾過ー濃縮ー冷却ー結晶採取ー乾燥の工程を経てジ
シアノ金酸カリウムの結晶を得た。
As the cathode, a metal plate (150 × 300 × 1 mm)
Two sheets were prepared and electrolyzed in a 20% potassium cyanide solution through a birefringent membrane at 60 ° C. and 160 A for 18 hours. As a result, 18.6
Kg was dissolved, and the dissolution rate was 86.5%. This solution was subjected to the steps of general filtration-concentration-cooling-crystal collection-drying to obtain crystals of potassium dicyanoaurate.

【0013】つぎに、比較として従来技術によって行っ
た例を以下に説明する。金地金27.8Kgを黒鉛坩堝中で加
熱溶解し、鋳造により150 ×300 ×8mm の極板4枚を製
造し、これを陽極とする。陰極としては、金板(150 ×
300 ×1mm )2枚を作り、素焼隔膜を介して20%シアン
化カリウム溶液中で、60℃、160Aで18時間電解した。
Next, as a comparison, an example of the conventional technique will be described below. 27.8 kg of gold metal is heated and melted in a graphite crucible, and four electrode plates of 150 × 300 × 8 mm are produced by casting, which is used as an anode. As the cathode, a gold plate (150 x
Two sheets (300 × 1 mm) were prepared and electrolyzed in a 20% potassium cyanide solution through a birefringent membrane at 60 ° C. and 160 A for 18 hours.

【0014】その結果、17.4Kgが溶解し、溶解率は62.3
% であった。この溶液を一般的な濾過ー濃縮ー冷却ー結
晶採取ー乾燥の工程を経てジシアノ金酸カリウムの結晶
を得た。
As a result, 17.4 Kg was dissolved and the dissolution rate was 62.3.
% Met. This solution was subjected to the steps of general filtration-concentration-cooling-crystal collection-drying to obtain crystals of potassium dicyanoaurate.

【0015】[0015]

【発明の効果】以上詳細に説明した本発明によると、粒
状に加工した金地金をチタン製容器に入れ、シアン化カ
リウム溶液の電解槽中に陽極としてセットし、陰極板を
隔膜を介してセットしたことにより、従来の板材の陽極
に比べ、溶解効率が大きく向上する効果を有し、粒状金
を追加補給するだけで連続して作業が可能となり、従来
の金板の取り付け、取り外しの作業が不要となる効果が
ある。
According to the present invention described in detail above, the granular metal ingot is placed in a titanium container, set as an anode in an electrolytic bath of a potassium cyanide solution, and a cathode plate is set via a diaphragm. As a result, it has the effect of greatly improving the melting efficiency compared to the conventional anode of the plate material, and it becomes possible to work continuously just by adding additional granular gold, and the work of attaching and detaching the conventional metal plate is unnecessary. There is an effect.

【0016】また、陽極は従来の板材に比べ粒材は製造
工程数が少なくてよいために高価な金地金を経済的に運
用することができる効果を有する。
Further, the anode has the effect that the expensive gold bullion can be economically operated because the number of manufacturing steps of the granular material is smaller than that of the conventional plate material.

【図面の簡単な説明】[Brief description of drawings]

【図1】電解液中に金板を陽極としたときの電流と電圧
の関係を示すグラフである。
FIG. 1 is a graph showing the relationship between current and voltage when a gold plate is used as an anode in an electrolytic solution.

【図2】陽極金板の表面積を変えたときの電流と電圧の
関係を示すグラフである。
FIG. 2 is a graph showing the relationship between current and voltage when the surface area of an anode metal plate is changed.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 粒状に加工した金地金をチタン製容器に
入れ、シアン化カリウム溶液の電解槽中に陽極としてセ
ットし、陰極板を隔膜を介してセットしたことを特徴と
するジシアノ金酸カリウムの製造方法。
1. A process for producing potassium dicyanoaurate characterized in that a granular metal ingot is placed in a titanium container, set as an anode in an electrolytic bath of a potassium cyanide solution, and a cathode plate is set through a diaphragm. Method.
JP34682792A 1992-12-25 1992-12-25 Method for producing potassium dicyanoaurate Expired - Lifetime JP3202375B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP34682792A JP3202375B2 (en) 1992-12-25 1992-12-25 Method for producing potassium dicyanoaurate

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP34682792A JP3202375B2 (en) 1992-12-25 1992-12-25 Method for producing potassium dicyanoaurate

Publications (2)

Publication Number Publication Date
JPH06192866A true JPH06192866A (en) 1994-07-12
JP3202375B2 JP3202375B2 (en) 2001-08-27

Family

ID=18386078

Family Applications (1)

Application Number Title Priority Date Filing Date
JP34682792A Expired - Lifetime JP3202375B2 (en) 1992-12-25 1992-12-25 Method for producing potassium dicyanoaurate

Country Status (1)

Country Link
JP (1) JP3202375B2 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1050607A2 (en) * 1999-05-06 2000-11-08 Josep Ferre Torres A method and an equipment for the electrolytic deposition of gold or gold alloys
KR101301526B1 (en) * 2012-02-02 2013-09-04 성일하이텍(주) Manufacturing method of potassium silver cyanide solution using air bubbling
CN109518210A (en) * 2018-11-29 2019-03-26 泰州市欣港电子材料有限公司 A kind of gold potassium cyanide production technology
KR20230132855A (en) 2021-01-26 2023-09-18 마츠다 산교 가부시끼가이샤 Method for producing gold potassium cyanide

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1050607A2 (en) * 1999-05-06 2000-11-08 Josep Ferre Torres A method and an equipment for the electrolytic deposition of gold or gold alloys
EP1050607A3 (en) * 1999-05-06 2002-11-13 Josep Ferre Torres A method and an equipment for the electrolytic deposition of gold or gold alloys
KR101301526B1 (en) * 2012-02-02 2013-09-04 성일하이텍(주) Manufacturing method of potassium silver cyanide solution using air bubbling
CN109518210A (en) * 2018-11-29 2019-03-26 泰州市欣港电子材料有限公司 A kind of gold potassium cyanide production technology
KR20230132855A (en) 2021-01-26 2023-09-18 마츠다 산교 가부시끼가이샤 Method for producing gold potassium cyanide

Also Published As

Publication number Publication date
JP3202375B2 (en) 2001-08-27

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