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用硅灰稳定零价铁纳米颗粒以增强其在水和土壤中六价铬的迁移和修复。

Stabilization of Fe(0) nanoparticles with silica fume for enhanced transport and remediation of hexavalent chromium in water and soil.

机构信息

College of Environmental Science and Engineering, Nankai University, Tianjin 300071, China.

出版信息

J Environ Sci (China). 2011;23(7):1211-8. doi: 10.1016/s1001-0742(10)60534-7.

Abstract

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+.

摘要

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+。

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