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Destruction of cyanide by hydrogen peroxide in tailings slurries from low bearing sulphidic gold ores

机译:低轴承硫化金矿石中尾矿浆中过氧化氢对氰化物的破坏

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摘要

The main objective of this work was to determine the effectiveness and kinetics of hydrogen peroxide in destroying cyanide in the tailings slurry from a gold mine with low sulphide and heavy metal content. The impacts of catalyst (Cu) and hydrogen peroxide concentrations, temperature and pH on the extent and rate of weak acid dissociable (WAD) cyanide destruction were investigated. Experiments were conducted using the variable-dose completely mixed batch reactor bottle-point method. Both the rate and extent of CN_(WAD) destruction generally increased with increasing peroxide doses for either absence or presence of Cu catalyst. Catalyst addition was very effective in terms of not only enhancing the cyanide destruction rate but also significantly reducing the required peroxide dosages to achieve CN_(WAD) concentrations of about 1 mg/1, independent of the temperatures tested (10, 20 and 30 °C). The initial cyanide destruction rates increased between 1.2 and 3 folds with the addition of 30 mg/1 of Cu. Kinetic experiments showed that in most cases little CN_(WAD) destruction occurred after a reaction time of 2-4 h. The impact of slurry pH on cyanide destruction varied depending upon the dosages of Cu catalyst. Relatively lower peroxide dose/ CN_(WAD) ratios required to achieve less than 1 mg/1 of CN_(WAD) niay be due to lower heavy metals and sulphide content of the ore, resulting in lower peroxide requirement for metal bound cyanides. During cyanide destruction, nitrate was initially formed as a by-product and then possibly converted to other some volatile nitrogen-containing species, as supported by the mass balance calculations.
机译:这项工作的主要目的是确定过氧化氢在破坏低硫化物和重金属含量的金矿的尾矿浆中氰化物中的有效性和动力学。研究了催化剂(Cu)和过氧化氢浓度,温度和pH对弱酸可分解(WAD)氰化物破坏程度和速率的影响。使用可变剂量完全混合间歇式反应器瓶点法进行实验。由于不存在或存在Cu催化剂,CN_(WAD)破坏的速率和程度通常都随着过氧化物剂量的增加而增加。催化剂的添加非常有效,不仅可以提高氰化物的破坏速度,而且还可以显着降低所需的过氧化物剂量,以使CN_(WAD)浓度达到约1 mg / 1,而与所测试的温度(10、20和30°C)无关)。加入30 mg / 1的Cu,初始氰化物破坏速率提高了1.2到3倍。动力学实验表明,在大多数情况下,2-4小时的反应时间后几乎不发生CN_(WAD)破坏。浆料pH对氰化物破坏的影响取决于Cu催化剂的用量。实现少于1 mg / 1的CN_(WAD)所需的过氧化物剂量/ CN_(WAD)比相对较低,这是由于矿石中的重金属和硫化物含量较低,从而导致金属结合氰化物的过氧化物需求量降低。在破坏氰化物的过程中,硝酸盐最初是作为副产物形成的,然后可能会转化为其他一些挥发性的含氮物质,这在质量平衡计算中得到了支持。

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