Maiti Sutanu, Neogi Sudarsan, Dutta Binay K
Indian Institute of Technology Kharagpur, Kharagpur, 721302, West Bengal, India.
Heliyon. 2023 Mar 29;9(4):e15009. doi: 10.1016/j.heliyon.2023.e15009. eCollection 2023 Apr.
Soil contaminated with hexavalent chromium seriously threatens the environment and human health. The use of FeS, which has a high redox activity and excellent reduction capacity, limits its application in soil remediation due to its premature surface oxidation and massive aggregation. To prevent premature surface oxidation and agglomeration, cetyltrimethylammonium bromide-supported nano-ferrous sulfide (CTAB-nFeS) was chemically synthesized and used for immobilizing Cr(VI) in contaminated soil. In order to evaluate the role of CTAB stabilization of nFeS and interaction mechanisms were investigated by XPS, FTIR, XRD, and FESEM. Batch experiments showed a complete reduction of Cr(VI) within 3 h with only 235% excess of CTAB-nFeS at a soil pH of 8 compared to days as reported in the literature with alternative FeS forms. The reduction kinetic data could be satisfactorily fitted into the second-order rate model. The rate constant linearly depends on the soil-to-water ratio, but its logarithmic form is linear in the given pH range. The oxidation-reduction potential increases with decreasing initial pH, thus positively impacting the reduction process. XPS analysis revealed the reduction process as multi-steps (reduction, adsorption, and co-precipitation). Ecological studies showed improved plant growth and earthworm survival rate in the remediated soil. Medium-term stability experiments suggested a significant decrease in TCLP leachate concentration of Cr after CTAB-nFeS treatment and remained stable for 60 d. Overall results of our study suggested a sustainable, feasible, and effective strategy for in-situ remediation of Cr(VI)-contaminated soil using CTAB-nFeS at natural pH.
被六价铬污染的土壤严重威胁着环境和人类健康。硫化亚铁具有高氧化还原活性和出色的还原能力,但由于其表面过早氧化和大量聚集,限制了其在土壤修复中的应用。为防止表面过早氧化和团聚,通过化学合成制备了十六烷基三甲基溴化铵负载的纳米硫化亚铁(CTAB-nFeS),并将其用于固定污染土壤中的Cr(VI)。为评估CTAB对nFeS的稳定作用及相互作用机制,采用XPS、FTIR、XRD和FESEM进行了研究。批次实验表明,在土壤pH值为8时,仅使用235%过量的CTAB-nFeS,3小时内即可将Cr(VI)完全还原,而相比文献中报道的其他硫化亚铁形式则需要数天时间。还原动力学数据能够很好地拟合二级速率模型。速率常数与土水比呈线性关系,但其对数形式在给定的pH范围内呈线性。氧化还原电位随着初始pH值的降低而升高,从而对还原过程产生积极影响。XPS分析表明还原过程为多步骤(还原、吸附和共沉淀)。生态研究表明,修复后的土壤中植物生长和蚯蚓存活率有所提高。中期稳定性实验表明,CTAB-nFeS处理后,TCLP浸出液中Cr的浓度显著降低,并在60天内保持稳定。我们研究的总体结果表明,在自然pH值下,使用CTAB-nFeS对Cr(VI)污染土壤进行原位修复是一种可持续、可行且有效的策略。