Key Laboratory of Coastal Environment Processes, Yantai Institute of Coastal Zone Research, Chinese Academy of Sciences, Yantai 264003, China.
State Key Laboratory of Environmental Aquatic Chemistry, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, P.O. Box 2871, Beijing 100085, China.
J Colloid Interface Sci. 2012 Jan 15;366(1):141-146. doi: 10.1016/j.jcis.2011.09.058. Epub 2011 Oct 1.
Arsenate retention, arsenite sorption and oxidation on the surfaces of Fe-Mn binary oxides may play an important role in the mobilization and transformation of arsenic, due to the common occurrence of these oxides in the environment. However, no sufficient information on the sorption behaviors of arsenic on Fe-Mn binary oxides is available. This study investigated the influences of Mn/Fe molar ratio, solution pH, coexisting calcium ions, and humic acids have on arsenic sorption by Fe-Mn binary oxides. To create Fe-Mn binary oxides, simultaneous oxidation and co-precipitation methods were employed. The Fe-Mn binary oxides exhibited a porous crystalline structure similar to 2-line ferrihydrite at Mn/Fe ratios 1:3 and below, whereas exhibited similar structures to δ-MnO(2) at higher ratios. The As(V) sorption maximum was observed at a Mn/Fe ratio of 1:6, but As(III) uptake maximum was at Mn/Fe ratio 1:3. However, As(III) adsorption capacity was much higher than that of As(V) at each Mn/Fe ratio. As(V) sorption was found to decrease with increasing pH, while As(III) sorption edge was different, depending on the content of MnO(2) in the binary oxides. The presence of Ca(2+) enhanced the As(V) uptake under alkaline pH, but did not significantly influence the As(III) sorption by 1:9 Fe-Mn binary oxide; whereas the presence of humic acid slightly reduced both As(V) and As(III) uptake. These results indicate that As(III) is more easily immobilized than As(V) in the environment, where Fe-Mn binary oxides are available as sorbents and they represent attractive adsorbents for both As(V) and As(III) removal from water and groundwater.
砷酸盐在铁锰二元氧化物表面的保留、砷酸盐吸附和氧化作用可能在砷的迁移和转化中起重要作用,因为这些氧化物在环境中普遍存在。然而,关于砷在铁锰二元氧化物上的吸附行为,目前还没有足够的信息。本研究考察了锰铁摩尔比、溶液 pH 值、共存钙离子和腐殖酸对铁锰二元氧化物吸附砷的影响。为了制备铁锰二元氧化物,采用了同时氧化共沉淀法。在锰铁摩尔比为 1:3 及以下时,铁锰二元氧化物呈现出类似于 2 线水铁矿的多孔结晶结构,而在更高的比例下则呈现出类似于 δ-MnO(2)的结构。在锰铁摩尔比为 1:6 时,观察到砷(V)的吸附最大值,但砷(III)的最大吸附量出现在锰铁摩尔比为 1:3 时。然而,在每个锰铁摩尔比下,砷(III)的吸附容量都远高于砷(V)。砷(V)的吸附随 pH 值的升高而降低,而砷(III)的吸附边缘则取决于二元氧化物中 MnO(2)的含量。在碱性 pH 值下,钙离子的存在增强了砷(V)的摄取,但对 1:9 铁锰二元氧化物中砷(III)的吸附没有显著影响;而腐殖酸的存在则略微降低了砷(V)和砷(III)的摄取量。这些结果表明,在铁锰二元氧化物可用作吸附剂的环境中,砷(III)比砷(V)更容易被固定,并且它们是从水中和地下水中去除砷(V)和砷(III)的有吸引力的吸附剂。