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首页> 外文期刊>Metallurgical Review of MMIJ >Purification of Zinc Leaching Solution-Mechanism of Removal of Cobalt by Zinc Dust with Arsenious Oxide and Copper Ion-
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Purification of Zinc Leaching Solution-Mechanism of Removal of Cobalt by Zinc Dust with Arsenious Oxide and Copper Ion-

机译:锌浸出液的纯化-氧化亚砷和铜离子去除锌粉中钴的机理

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摘要

Cobalt precipitation by zinc dust with co-addition of arsenious oxide and copper ion in a practical operation was simulated by the experiments using a galvanic cell with a diaphragm and this mechanism for removal of cobalt was explained as follows; a galvanic cell was formed between zinc dust and copper particles, which were precipitated first by zinc dust and cobalt is deposited on copper particles by this galvanic cell and arsenious oxide in a solution accelerated the rate of predication of cobalt by co-depositor of AS-CQ. The anode side reaction of this galvanic cell is Zn = Zn~(2+) + 2e and a main cathode reaction is 2H~+ + 2e = H2(g). Cobalt is difficult to be precipitated on copper without arsenious oxide. The galvanic current between zinc and copper becomes higher by addition of arsenious oxide. The over potential of the cathode reaction sifts the cathode potential to be lower potential than the deposition potential of Co-As, and this Co-As easily deposits on copper cathode with hydrogen.
机译:在实际操作中,通过使用带有隔膜的原电池进行的实验模拟了锌粉在钴与砷氧化物和铜离子的共同沉淀下的沉淀过程,该机理如下:锌粉和铜颗粒之间形成了一个原电池,锌粉首先沉淀了该锌电池,并且钴在该原电池上沉积在铜颗粒上,溶液中的氧化砷加快了AS-的共沉积剂对钴的预测速度。 CQ。该原电池的阳极侧反应为Zn = Zn〜(2+)+ 2e,主阴极反应为2H〜+ + 2e = H2(g)。没有亚砷氧化物,钴很难在铜上沉淀。锌和铜之间的电流通过添加砷氧化物而变得更高。阴极反应的过电位将阴极电位筛选为比Co-As的沉积电位低的电位,并且该Co-As容易与氢沉积在铜阴极上。

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