Effects of the iron oxidation and precipitation processes on the arsenate sorption and coprecipitation

Ivelina Moteva, P. Georgiev
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Abstract

The main aim of this study was to assess the effects of ferrous iron oxidation, hydrolysis and precipitation of the ferric iron on the mechanisms of arsenate removal from acid mine drainage. The study was realized at the pH range 2,0 – 6,5. H2O2 was the oxidant used in the chemical test. A mixed culture of mesophilic iron-oxidizing chemolithotrophic bacteria (Acidithiobacillus ferrooxidans, Leptospirillum ferroxidans) carried out the ferrous oxidation in the biological test. NaOH was used as an alkalizing agent which triggered the ferric iron hydrolysis and precipitation. The results showed that the total content of retained arsenic by ferric iron hydrous oxides and its speciation as geochemical fractions depended on the iron and phosphate concentrations in acid solution. The results showed that phosphate concentration lower than 6 mg/ L limited the ferrous iron oxidation rate. At the tested experimental conditions, arsenic sorption by formed ferric iron hydrous oxides was the main mechanism for its removal from acid mine drainage, as the ratio between iron and phosphate determined the proportions between the geochemical fractions of scavenged arsenic.
铁氧化和沉淀过程对砷酸盐吸附和共沉淀的影响
本研究的主要目的是评价亚铁氧化、水解和沉淀对酸性矿井水中砷酸盐去除机理的影响。研究在pH值为2,0 - 6,5的范围内完成。H2O2是化学试验中使用的氧化剂。在生物试验中,嗜酸性氧化亚铁硫杆菌、氧化亚铁钩端螺旋体等嗜酸性氧化铁化嗜石菌进行了亚铁氧化的混合培养。以NaOH为碱化剂,催化铁的水解和沉淀。结果表明:三氧化铁中砷的总含量及其地球化学组分的形态与酸溶液中铁和磷酸盐的浓度有关;结果表明,磷酸盐浓度低于6 mg/ L时,亚铁的氧化速率受到限制。在所测试的实验条件下,形成的氧化铁对砷的吸附是酸性矿井水中砷的主要去除机制,铁与磷酸盐的比值决定了清除砷的地球化学组分的比例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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