Key Laboratory of Arable Land Conservation (Middle and Lower Reaches of Yangtse River), Ministry of Agriculture, College of Resources and Environment, Huazhong Agricultural University, Wuhan, 430070, China; State Key Laboratory of Silicate Materials for Architectures, Wuhan University of Technology, Wuhan, 430070, China.
Key Laboratory of Arable Land Conservation (Middle and Lower Reaches of Yangtse River), Ministry of Agriculture, College of Resources and Environment, Huazhong Agricultural University, Wuhan, 430070, China.
Environ Pollut. 2018 Jul;238:524-531. doi: 10.1016/j.envpol.2018.03.047. Epub 2018 Mar 30.
Cryptomelane-type octahedral molecular sieve manganese oxide (OMS-2) possesses high redox potential and has attracted much interest in its application for oxidation arsenite (As(III)) species of arsenic to arsenate (As(V)) to decrease arsenic toxicity and promote total arsenic removal. However, coexisting ions such as As(V) and phosphate are ubiquitous and readily bond to manganese oxide surface, consequently passivating surface active sites of manganese oxide and reducing As(III) oxidation. In this study, we present a novel strategy to significantly promote As(III) oxidation activity of OMS-2 by tuning K concentration in the tunnel. Batch experimental results reveal that increasing K concentration in the tunnel of OMS-2 not only considerably improved As(III) oxidation kinetics rate from 0.027 to 0.102 min, but also reduced adverse effect of competitive ion on As(III) oxidation. The origin of K concentration effect on As(III) oxidation was investigated through As(V) and phosphate adsorption kinetics, detection of Mn release in solution, surface charge characteristics, and density functional theory (DFT) calculations. Experimental results and theoretical calculations confirm that by increasing K concentration in the OMS-2 tunnel not only does it improve arsenic adsorption on K doped OMS-2, but also accelerates two electrons transfers from As(III) to each bonded Mn atom on OMS-2 surface, thus considerably improving As(III) oxidation kinetics rate, which is responsible for counteracting the adverse adsorption effects by coexisting ions.
钙锰矿型八面体分子篮型氧化锰(OMS-2)具有较高的氧化还原电位,在将砷的亚砷酸盐(As(III))氧化为砷酸盐(As(V))以降低砷毒性和促进总砷去除方面的应用引起了广泛关注。然而,As(V)和磷酸盐等共存离子普遍存在,容易与氧化锰表面键合,从而钝化氧化锰表面的活性位点,降低 As(III)的氧化速率。在本研究中,我们提出了一种通过调变隧道中 K 浓度来显著提高 OMS-2 氧化 As(III)活性的新策略。批量实验结果表明,隧道中 K 浓度的增加不仅极大地提高了 As(III)的氧化动力学速率(从 0.027 提高至 0.102 min),而且降低了竞争离子对 As(III)氧化的不利影响。通过 As(V)和磷酸盐吸附动力学、溶液中 Mn 释放的检测、表面电荷特性和密度泛函理论(DFT)计算,研究了 K 浓度对 As(III)氧化的影响。实验结果和理论计算均证实,通过增加 OMS-2 隧道中的 K 浓度,不仅提高了 K 掺杂 OMS-2 对砷的吸附,而且促进了两个电子从 As(III)转移到 OMS-2 表面每个键合的 Mn 原子上,从而极大地提高了 As(III)的氧化动力学速率,这有助于抵消共存离子的不利吸附影响。