Laboratory of Separation and Reaction Engineering - Laboratory of Catalysis and Materials (LSRE-LCM), Departamento de Engenharia Química, Faculdade de Engenharia da Universidade do Porto, Rua Dr. Roberto Frias, 4200-465 Porto, Portugal.
Laboratory of Separation and Reaction Engineering - Laboratory of Catalysis and Materials (LSRE-LCM), Departamento de Engenharia Química, Faculdade de Engenharia da Universidade do Porto, Rua Dr. Roberto Frias, 4200-465 Porto, Portugal.
Sci Total Environ. 2018 Nov 15;642:1075-1089. doi: 10.1016/j.scitotenv.2018.06.170. Epub 2018 Jun 20.
There is a growing demand for low-cost, effective adsorbents for arsenic removal from water intended for human consumption in affected rural areas. This work presents a novel adsorbent based on the coating of cork granulates with iron (oxy)hydroxides for the removal of As(III) and As(V) from aqueous matrices. A 2 fractional factorial design was used to determine the optimal conditions for the iron coating procedure. The optimal adsorbent was produced by coating low-density cork granulates with iron (oxy)hydroxides precipitated from a 0.05 mol L FeCl solution at pH 7, 20 °C temperature and 20 g L S/L ratio, in a single coating cycle. Arsenic adsorption was found to be dependent on pH, with inverse trends for As(III) and As(V). The iron leaching from the adsorbent was also taken into account to select the optimum pH, which was pH 9 for As(III) and pH 3 for As(V). Adsorption kinetics were better described by the pseudo-second-order model for As(III) and the Elovich model for As(V). Equilibrium was reached in 16 h for As(III) at pH 9 and 48 h for As(V) at pH 3. The isotherm models indicated different adsorption behaviours for As(III) and As(V), with better fits by Langmuir and Freundlich models, respectively. The Langmuir maximum adsorption capacity of iron-coated cork adsorbent for As(III) at pH 9 was 4.9 ± 0.3 mg g. However, at low equilibrium concentrations, As(V) adsorption was higher than As(III) (e.g. 2.1 ± 0.2 mg g in equilibrium with 0.16 ± 0.03 mg L). Speciation studies and XPS analyses indicated that no substantial oxidation of As(III) to As(V) occurred during the adsorption process. The study shows that iron coating can enhance both arsenate and arsenite adsorption capacity of cork materials, leading to an innovative natural adsorbent with high resilience and stability, with possible application in arsenic remediation.
在受影响的农村地区,人们越来越需要从饮用水中去除砷的低成本、高效吸附剂,以用于人类消费。本工作提出了一种基于在软木颗粒上涂覆铁(氧)氢氧化物的新型吸附剂,用于从水基质中去除 As(III) 和 As(V)。使用 2 分数阶因子设计来确定铁涂层程序的最佳条件。通过在 pH 7、20°C 温度和 20 g L S/L 比下,在单个涂层循环中,用从 0.05 mol L FeCl 溶液沉淀的铁(氧)氢氧化物涂覆低密度软木颗粒,制备出最佳吸附剂。发现砷吸附依赖于 pH,As(III) 和 As(V) 的趋势相反。还考虑了从吸附剂中浸出的铁来选择最佳 pH,对于 As(III) 为 pH 9,对于 As(V) 为 pH 3。对于 As(III),吸附动力学更好地由准二级模型描述,对于 As(V),由 Elovich 模型描述。在 pH 9 下,16 h 即可达到 As(III)的平衡,在 pH 3 下,48 h 即可达到 As(V)的平衡。等温线模型表明,As(III)和 As(V)的吸附行为不同,分别由 Langmuir 和 Freundlich 模型更好地拟合。在 pH 9 下,铁涂覆软木吸附剂对 As(III)的最大吸附容量为 4.9 ± 0.3 mg g。然而,在低平衡浓度下,As(V)的吸附高于 As(III)(例如,在 0.16 ± 0.03 mg L 的平衡浓度下为 2.1 ± 0.2 mg g)。形态研究和 XPS 分析表明,在吸附过程中没有发生大量 As(III)向 As(V)的氧化。该研究表明,铁涂层可以提高软木材料对砷酸盐和亚砷酸盐的吸附能力,从而得到一种具有高弹性和稳定性的新型天然吸附剂,可能在砷修复中得到应用。