State Key Laboratory of Biogeology and Environmental Geology, China University of Geosciences , Beijing 100083, P.R. China.
School of Water Resources and Environment, China University of Geosciences , Beijing 100083, P.R. China.
Environ Sci Technol. 2016 Jun 21;50(12):6449-58. doi: 10.1021/acs.est.6b00562. Epub 2016 Jun 3.
An anaerobic nitrate-reducing Fe(II)-oxidizing bacterium, Pseudogulbenkiania sp. strain 2002, was used to investigate As immobilization by biogenic Fe oxyhydroxides under different initial molar ratios of Fe/As in solutions. Results showed that Fe(II) was effectively oxidized, mainly forming lepidocrocite, which immobilized more As(III) than As(V) without changing the redox state of As. When the initial Fe/As ratios were kept constant, higher initial Fe(II) concentrations immobilized more As with higher Asimmobilized/Feprecipitated in biogenic lepidocrocite. EXAFS analysis showed that variations of initial Fe(II) concentrations did not change the As-Fe complexes (bidentate binuclear complexes ((2)C)) with a fixed As(III) or As(V) initial concentration of 13.3 μM. On the other hand, variations in initial As concentrations but fixed Fe(II) initial concentration induced the co-occurrence of bidentate binuclear and bidentate mononuclear complexes ((2)E) and bidentate binuclear and monodentate mononuclear complexes ((1)V) for As(III) and As(V)-treated series, respectively. The coexistence of (2)C and (2)E complexes (or (2)C and (1)V complexes) could contribute to higher As removal in experimental series with higher initial Fe(II) concentrations at the same initial Fe/As ratio. Simultaneous removal of soluble As and nitrate by anaerobic nitrate-reducing Fe(II)-oxidizing bacteria provides a feasible approach for in situ remediation of As-nitrate cocontaminated groundwater.
一种厌氧硝酸盐还原的 Fe(II)氧化细菌,假浮霉菌 2002 株,用于研究不同初始铁砷摩尔比条件下生物成因的 Fe 氧氢氧化物对砷的固定作用。结果表明,Fe(II)被有效氧化,主要形成纤铁矿,固定了更多的 As(III)而不是 As(V),同时不改变砷的氧化还原状态。当初始 Fe/As 比保持不变时,较高的初始 Fe(II)浓度在生物成因的纤铁矿中固定了更多的砷,同时砷固定/铁沉淀的比例也更高。EXAFS 分析表明,初始 Fe(II)浓度的变化并不改变砷铁配合物(双齿双核配合物((2)C)),初始砷浓度固定为 13.3 μM。另一方面,初始砷浓度的变化而固定的 Fe(II)初始浓度诱导了双齿双核和双齿单核配合物((2)E)以及双齿双核和单齿单核配合物((1)V)的共同出现,分别用于 As(III)和 As(V)处理系列。(2)C 和 (2)E 配合物(或(2)C 和 (1)V 配合物)的共存可能有助于在相同初始 Fe/As 比下,初始 Fe(II)浓度较高的实验系列中实现更高的砷去除。厌氧硝酸盐还原的 Fe(II)氧化细菌同时去除可溶性砷和硝酸盐,为原位修复砷硝酸盐共污染地下水提供了一种可行的方法。