College of Environmental Science and Engineering, Nankai University, Tianjin 300071, China.
J Environ Sci (China). 2011;23(7):1211-8. doi: 10.1016/s1001-0742(10)60534-7.
Effective in situ remediation of Cr(VI) in groundwater requires the successful delivery of reactive iron particles to the subsurface. Fe(0) nanoparticles (20-110 nm diameter) supported on silica fume were synthesized by borohydride reduction of an aqueous iron salt in the presence of a support material. The experimental result showed that attachment of Fe(0) nanoparticles on the commercial available sub-micrometer silica fume prevented them from aggregation while maintaining the particle reactivity. When the Fe(0) concentration was 0.4 g/L, 88.00% of 40 mg/L Cr(VI) was removed by silica fume-supported Fe(0) nanoparticles (SF-Fe(0) in 120 min, 22.55% higher than unsupported Fe(0). Furthermore, transport experiments confirmed that almost all unsupported Fe(0) was retained, whereas 51.50% and 38.29% of SF-Fe(0) were eluted from the vertical and horizontal sand column, respectively. Additionally, the effect of solution ionic strength on the transport ability of SF-Fe(0) was evaluated. The result showed that increase in the salt concentration led to a decrease in the mobility and also the divalent ion Ca2+ had a greater effect than that of monovalent ion Na+.
要有效地原位修复地下水中的六价铬,需要成功地将反应性铁颗粒输送到地下。在载体材料存在下,通过硼氢化钠还原水溶液中的铁盐,合成了负载在硅灰上的 Fe(0)纳米颗粒(直径 20-110nm)。实验结果表明,商业上可用的亚微米硅灰上负载的 Fe(0)纳米颗粒的附着防止了它们的聚集,同时保持了颗粒的反应性。当 Fe(0)浓度为 0.4g/L 时,在 120min 内,40mg/L 的六价铬有 88.00%被硅灰负载的 Fe(0)纳米颗粒(SF-Fe(0))去除,比未负载的 Fe(0)高 22.55%。此外,运输实验证实,几乎所有未负载的 Fe(0)都被截留,而 SF-Fe(0)分别有 51.50%和 38.29%从垂直和水平砂柱中洗脱出来。此外,还评估了溶液离子强度对 SF-Fe(0)输送能力的影响。结果表明,盐浓度的增加导致迁移率降低,而且二价离子 Ca2+的影响大于一价离子 Na+。