College of Resource and Environmental Engineering, Wuhan University of Science and Technology, Wuhan 430081, China and Hubei Key Laboratory for Efficient Utilization and Agglomeration of Metallurgic Mineral Resources, Wuhan University of Science and Technology, Wuhan 430081, China E-mail:
Research Institute for Environmental Innovation (Suzhou), Tsinghua, Suzhou 215011, China.
Water Sci Technol. 2021 Jun;83(12):2886-2900. doi: 10.2166/wst.2021.184.
Nanoscale zero-valent iron (nZVI) and sulfides have been confirmed to be effective in arsenic sequestration from aqueous solution. In this study, attapulgite supported and sulfide-modified nanoscale zero-valent iron (S-nZVI@ATP) are synthesized to realize the superposition effect of enhanced arsenic sequestration. The results indicated that nZVI clusters were well disaggregated and the BET specific surface area increased from 19.61 m·g to 46.04 m·g of S-nZVI@ATP, resulting in an enhanced removal efficiency of arsenic from 51.4% to 65.1% at 20 min. The sulfides in S-nZVI@ATP mainly exist as mackinawite (FeS) and this causes the spherical nanoparticles to exhibit a larger average particle size (94.6 nm) compared to bare nZVI (66.0 nm). In addition, S-nZVI@ATP exhibited a prominent ability for arsenic sequestration over a wide pH range of 3.0-6.0. The presence of anions SO and Cl can enhance the arsenic removal whereas HCO inhibited it. The arsenic adsorption by S-nZVI@ATP could be explained by the pseudo-second-order kinetic model and the Langmuir model, with the maximum adsorption capacity of 193.8 mg·g. The mechanism of As(III) sequestration by S-nZVI@ATP involved multiple processes, mainly including precipitation conversion from FeS to AsS, surface-complexation adsorption and co-precipitation.
纳米零价铁(nZVI)和硫化物已被证实可有效从水溶液中固定砷。本研究制备了凹凸棒石负载和硫化物改性的纳米零价铁(S-nZVI@ATP),以实现增强砷固定的叠加效应。结果表明,nZVI 团聚体被很好地分散,BET 比表面积从 19.61 m·g 增加到 46.04 m·g 的 S-nZVI@ATP,导致 20 分钟时砷的去除效率从 51.4%提高到 65.1%。S-nZVI@ATP 中的硫化物主要以磁黄铁矿(FeS)的形式存在,这导致球形纳米颗粒的平均粒径(94.6nm)大于裸 nZVI(66.0nm)。此外,S-nZVI@ATP 在 3.0-6.0 的宽 pH 范围内表现出突出的砷固定能力。阴离子 SO 和 Cl 的存在可以增强砷的去除,而 HCO 则抑制了砷的去除。S-nZVI@ATP 对砷的吸附可以用伪二级动力学模型和 Langmuir 模型来解释,最大吸附容量为 193.8mg·g。S-nZVI@ATP 固定 As(III)的机制涉及多个过程,主要包括 FeS 向 AsS 的沉淀转化、表面络合吸附和共沉淀。