Gheju M, Iovi A, Balcu I
Faculty of Industrial Chemistry and Environmental Engineering, Politehnica University of Timisoara, Timisoara, Romania.
J Hazard Mater. 2008 May 1;153(1-2):655-62. doi: 10.1016/j.jhazmat.2007.09.009. Epub 2007 Sep 6.
The reduction of hexavalent chromium by scrap iron was investigated in continuous system, using long-term column experiments, for aqueous Cr(VI) solutions having low buffering capacities, over the pH range of 2.00-7.30. The results showed that the initial pH of Cr(VI) solution significantly affects the reduction capacity of scrap iron. The highest reduction capacity was determined to be 19.2 mg Cr(VI)/g scrap iron, at pH 2.50, and decreased with increasing the initial pH of Cr(VI) solution. A considerable decrease in scrap iron reduction capacity (25%) was also observed at pH 2.00, as compared to pH 2.50, due to the increased contribution of H(+) ions to the corrosion of scrap iron, which leads to a rapid decrease in time of the scrap iron volume. Over the pH range of 2.50-7.30, hexavalent chromium concentration increases slowly in time after its breakthrough in column effluent, until a steady-state concentration was observed; similarly, over the same pH range, the amount of solubilized Cr(III) in treated column effluent decreases in time, until a steady-state concentration was observed. The steady-state concentration in column effluent decreased for Cr(VI) and increased for Cr(III) with decreasing the initial pH of Cr(VI) solution. No steady-state Cr(VI) or Cr(III) concentrations in column effluent were observed at pH 2.00. Over the entire studied pH range, the amount of Fe(total) in treated solution increases as the initial pH of column influent is decreased; the results show also a continuously decrease in time of Fe(total) concentration, for a constant initial pH, due to a decrease in time of iron corrosion rate. Cr(III) concentration in column effluent also continuously decreased in time, for a constant initial pH, over the pH range of 2.50-7.30. This represents an advantage, because the amount of precipitant agent used to remove Fe(total) and Cr(III) from the column effluent will also decrease in time. The optimum pH for Cr(VI) reduction with scrap iron in continuous-flow system was established at the value of 2.50.
采用长期柱实验,在连续体系中研究了低缓冲容量的含铬(VI)水溶液在pH值为2.00 - 7.30范围内,废铁对六价铬的还原作用。结果表明,铬(VI)溶液的初始pH值对废铁的还原能力有显著影响。在pH值为2.50时,废铁的最高还原能力为19.2 mg Cr(VI)/g废铁,且随着铬(VI)溶液初始pH值的升高而降低。与pH值为2.50相比,在pH值为2.00时,废铁的还原能力也显著下降(25%),这是由于H(+)离子对废铁腐蚀的贡献增加,导致废铁体积迅速减少。在pH值为2.50 - 7.30范围内,六价铬在柱流出物中穿透后,其浓度随时间缓慢增加,直至观察到稳态浓度;同样,在相同pH范围内,处理后的柱流出物中溶解的Cr(III)量随时间减少,直至观察到稳态浓度。随着铬(VI)溶液初始pH值的降低,柱流出物中Cr(VI)的稳态浓度降低,Cr(III)的稳态浓度升高。在pH值为2.00时,未观察到柱流出物中Cr(VI)或Cr(III)的稳态浓度。在整个研究的pH范围内,随着柱进水初始pH值的降低,处理后溶液中的Fe(总量)增加;结果还表明,在初始pH值恒定的情况下,由于铁腐蚀速率随时间降低,Fe(总量)浓度随时间持续下降。在pH值为2.50 - 7.30范围内,对于恒定的初始pH值,柱流出物中的Cr(III)浓度也随时间持续下降。这是一个优点,因为用于从柱流出物中去除Fe(总量)和Cr(III)的沉淀剂用量也会随时间减少。在连续流动体系中,用废铁还原Cr(VI)的最佳pH值确定为2.50。