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Decomposition of hydrogen peroxide in alkaline cyanide solutions

机译:碱性氰化物溶液中过氧化氢的分解

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Although oxygen is widely employed as the oxidant of choice in gold leaching by cyanide, its low aqueous solubility presents some drawbacks in practical application; hydrogen peroxide has therefore been considered as a possible alternative. The aim of this investigation was to study the catalytic decomposition of hydrogen peroxide, which generates an oxidizing intermediate species, and to understand its effect on cyanide destruction. Operating conditions that facilitated the effective decomposition of hydrogen peroxide were established by varying the pH and catalyst type and concentration. The oxidizing intermediate, detected using an indirect technique, was found to be the hydroxyl radical (OH). OH' is commonly generated in acidic solutions, but this work demonstrated that it is also produced at the alkaline pH values necessary for cyanide gold leaching. The effects of free and complexed iron and copper catalysts on the oxidation and consumption of hydrogen peroxide and cyanide were also investigated. It was shown that the cyano complexes of Fe(II) and Cu(I) are also effective as decomposition catalysts. Hydrogen peroxide concentrations above 0.01 M decreased the free cyanide concentration, which was attributed to the probable formation of the cyanate anion (CNO-). Although cyanide consumption increased due to its oxidation in the presence of OH', excessive cyanide consumption in the presence of copper was attributed primarily to its complexation by the unstable copper(I) cyanide species. Rate constants for the decompositions of H2O2 and cyanide by ferrocyanide and copper cyanide were calculated; the latter was identified as being a better catalyst
机译:虽然氧气广泛使用作为氰化物的金色浸出中的选择的氧化剂,但其低水溶性在实际应用中具有一些缺点;因此,过氧化氢被认为是可能的替代方案。该研究的目的是研究过氧化氢催化分解,其产生氧化中间体物种,并了解其对氰化物破坏的影响。通过改变pH和催化剂类型和浓度,建立促进有效分解过氧化氢的有效分解的操作条件。发现使用间接技术检测的氧化中间体是羟基自由基(OH)。 OH'通常在酸性溶液中产生,但是这项工作表明它也在氰化物金浸出所需的碱性pH值中产生。还研究了自由和络合物铁和铜催化剂对过氧化氢和氰化氰化物的氧化和消耗的影响。结果表明,Fe(II)和Cu(I)的氰基复合物也是分解催化剂的有效性。 0.01μm以上的过氧化氢浓度降低了自由的氰化物浓度,其归因于氰酸酯阴离子(CNO-)的可能形成。虽然氰化物消耗由于其氧化在OH'存在下,但在铜存在下过量的氰化物消耗主要归因于不稳定的铜(I)氰化物物种的络合。用氰化氰化物和氰化铜的H2O2和氰化物分解的速率常数;后者被鉴定为更好的催化剂

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