阴离子及相关有机化合物对太阳诱导氧化系统中硫氰酸盐氧化动力学的影响

IF 0.5 Q4 CHEMISTRY, MULTIDISCIPLINARY
Agnia A. Batoeva
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引用次数: 0

摘要

以自然太阳光为辐射源,研究了阴离子(碳酸盐、氯化物、硫酸盐)和有机化合物(黄药)对过硫酸铁体系中硫氰酸盐氧化动力学的影响。结果表明,阴离子的引入抑制了硫氰酸酯的降解。碳酸盐的作用最大,因此在HCO-3浓度为1 mM时,硫氰酸酯完全破坏所需的处理时间从6分钟增加到15.7分钟。在高浓度碳酸氢盐(≥5 mM)下,硫氰酸酯的氧化效率不超过52%。在溶液中加入丁基黄药对硫氰酸酯的光化学氧化无显著影响。在真实的水基质中(自来水和金矿厂尾矿库的循环水),氧化过程明显减慢。在自来水中,这种影响主要是由于碳酸盐的影响,而在废水中,这是由于水基质的多组分性质。硫氰酸酯废水处理效率为100%,COD - 82%,溶解有机碳- 65%。处理后未发现氰化物
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of Anions and Related Organic Compounds on the Kinetics of Thiocyanate Oxidation in a Solar-induced Oxidative System
The effect of anions (hydrocarbonates, chlorides, sulfates) and organic compounds (xanthates) on the kinetics of thiocyanate oxidation in a photoinduced iron-persulfate system was studied using natural sunlight as a radiation source. It was found that the introduction of anions into the solution inhibits the degradation of thiocyanates. Hydrocarbonates have the maximum effect, so at a HCO–3 concentration of 1 mM, the processing time required for the complete destruction of thiocyanates increased from 6 to 15.7 minutes. At high concentrations of bicarbonates (≥5 mM), the oxidation efficiency of thiocyanates does not exceed 52 %. The adding of butyl xanthate into the solution has no significant effect on the photochemical oxidation of thiocyanates. In real water matrices (tap water and circulating water of the tailing dump of a gold mining plant), oxidative processes are significantly slowed down. In tap water, this effect is mainly due to the influence of hydrocarbonates, and in waste water, it is due to the multicomponent nature of the water matrix. The efficiency of wastewater treatment from thiocyanates was 100 %, for COD – 82 %, for dissolved organic carbon – 65 %. No cyanides were found after the treatment
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来源期刊
CiteScore
1.10
自引率
0.00%
发文量
13
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