Liu Fenwu, Zhou Jun, Zhang Shasha, Liu Lanlan, Zhou Lixiang, Fan Wenhua
Environmental Engineering Laboratory, College of Resource and Environment, Shanxi Agricultural University, Taigu, China.
College of Biotechnology and Pharmaceutical Engineering, Nanjing Tech University, Nanjing, China.
PLoS One. 2015 Sep 23;10(9):e0138891. doi: 10.1371/journal.pone.0138891. eCollection 2015.
Schwertmannite-mediated removal of arsenic from contaminated water has attracted increasing attention. However, schwertmannite chemical synthesis behavior under different H2O2 supply rates for ferrous ions oxidation is unclear. This study investigated pH, ferrous ions oxidation efficiency, and total iron precipitation efficiency during schwertmannite synthesis by adding H2O2 into FeSO4 · 7H2O solution at different supply rates. Specific surface area and arsenic (III) removal capacity of schwertmannite have also been studied. Results showed that pH decreased from ~3.48 to ~1.96, ~2.06, ~2.12, ~2.14, or ~2.17 after 60 h reaction when the ferrous ions solution received the following corresponding amounts of H2O2: 1.80 mL at 2 h (treatment 1); 0.90 mL at 2 h and 14 h (treatment 2); 0.60 mL at 2, 14, and 26 h (treatment 3); 0.45 mL at 2, 14, 26, and 38 h (treatment 4), or 0.36 mL at 2, 14, 26, 38, and 50 h (treatment 5). Slow H2O2 supply significantly inhibited the total iron precipitation efficiency but improved the specific surface area or arsenic (III) removal capacity of schwertmannite. For the initial 50.0 μg/L arsenic (III)-contaminated water under pH ~7.0 and using 0.25 g/L schwertmannite as an adsorbent, the total iron precipitation efficiency, specific surface area of the harvested schwertmannite, and schwertmannite arsenic(III) removal efficiency were 29.3%, 2.06 m2/g, and 81.1%, respectively, in treatment 1. However, the above parameters correspondingly changed to 17.3%, 16.30 m2/g, and 96.5%, respectively, in treatment 5.
施韦特曼石介导的从受污染水中去除砷的方法已引起越来越多的关注。然而,在不同过氧化氢供应速率下,亚铁离子氧化过程中施韦特曼石的化学合成行为尚不清楚。本研究通过以不同供应速率向硫酸亚铁·7水合物溶液中添加过氧化氢,研究了施韦特曼石合成过程中的pH值、亚铁离子氧化效率和总铁沉淀效率。还研究了施韦特曼石的比表面积和砷(III)去除能力。结果表明,当亚铁离子溶液分别接受以下相应量的过氧化氢时,反应60小时后pH值从约3.48降至约1.96、约2.06、约2.12、约2.14或约2.17:2小时时1.80 mL(处理1);2小时和14小时时0.90 mL(处理2);2、14和26小时时0.60 mL(处理3);2、14、26和38小时时0.45 mL(处理4),或2、14、26、38和50小时时0.36 mL(处理5)。缓慢供应过氧化氢显著抑制了总铁沉淀效率,但提高了施韦特曼石的比表面积或砷(III)去除能力。对于初始浓度为50.0 μg/L砷(III)的受污染水,在pH约为7.0且使用0.25 g/L施韦特曼石作为吸附剂的情况下,处理1中收获的施韦特曼石的总铁沉淀效率、比表面积和砷(III)去除效率分别为29.3%、2.06 m²/g和81.1%。然而,在处理5中,上述参数分别相应变为17.3%、16.30 m²/g和96.5%。