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Heterogeneous catalytic degradation of cyanide using copper-impregnated pumice and hydrogen peroxide

机译:铜浸渍浮石和过氧化氢对氰化物的多相催化降解

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The main objective of this research was to investigate the oxidative destruction of free cyanide with hydrogen peroxide and copper-impregnated pumice as a heterogeneous catalyst. Original or copper-impregnated pumices added alone were not effective adsorbents of negatively charged cyanide ions due to incompatible surface interactions. Peroxide and original pumices added together were also ineffective in removing cyanide. However, for all of the three natural pumices tested with various particle size fractions, the use of copper-impregnated pumices and peroxide together significantly enhanced both the initial rate and extent of cyanide removal. Although copper-impregnated specific surface area was the major factor affecting the rate and extent of cyanide destruction for a particular pumice source with similar surface chemistries, the type of surface chemistry (i.e., specific functional groups) within different pumice sources also appears to be a very important factor. Lower rates and extents of cyanide removals were observed at pH 11 compared to pH 8 probably because of the negative impacts of alkaline conditions in terms of scavenging peroxide and forming more negatively charged pumice surfaces. Both the initial rate and ultimate extent of cyanide removals were generally higher at a temperature of 20℃ compared with those found at 10℃. The use of copper-impregnated pumice as a light, cheap, readily available, natural, and porous heterogeneous catalyst either in completely mixed/suspended or fixed-bed reactor configurations may be an effective treatment technology for cyanide removal from solution. This new approach may minimize downstream metal removal problems experienced in conventional cyanide oxidation technologies.
机译:这项研究的主要目的是研究过氧化氢和铜浸渍浮石作为非均相催化剂对游离氰化物的氧化破坏。由于不相容的表面相互作用,单独添加原始或浸铜的浮石不是带负电荷的氰化物离子的有效吸附剂。过氧化物和原始浮渣加在一起也不能有效去除氰化物。但是,对于以不同粒度级分测试的所有三种天然粉煤灰,将铜浸渍的粉煤灰和过氧化物一起使用可显着提高初始速度和氰化物去除率。尽管浸铜的比表面积是影响具有相似表面化学性质的特定浮石来源氰化物破坏速率和程度的主要因素,但不同浮石来源中的表面化学类型(即特定的官能团)似乎也是非常重要的因素。与pH 8相比,在pH 11处观察到较低的氰化物去除速率和程度,这可能是因为碱性条件对清除过氧化物和形成更多带负电荷的浮石表面具有负面影响。在20℃的温度下,氰化物去除的初始速率和最终去除程度通常都比在10℃的温度下更高。完全混合/悬浮或固定床反应器配置中使用铜浸渍浮石作为轻质,便宜,易于获得的天然和多孔非均相催化剂可能是从溶液中去除氰化物的有效处理技术。这种新方法可以最大程度地减少常规氰化物氧化技术中遇到的下游金属去除问题。

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