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用于从饮用水中去除砷的铁介质上砷酸盐和水还原的电化学研究。

Electrochemical study of arsenate and water reduction on iron media used for arsenic removal from potable water.

作者信息

Melitas Nikos, Conklin Martha, Farrell James

机构信息

Department of Chemical and Environmental Engineering, University of Arizona, Tucson 85721, USA.

出版信息

Environ Sci Technol. 2002 Jul 15;36(14):3188-93. doi: 10.1021/es0157595.

Abstract

Zerovalent iron filings have been proposed as a filter medium for removing As(III) and As(V) compounds from potable water. The removal mechanism involves complex formation of arsenite and arsenate with the iron surface and with iron oxides produced from iron corrosion. There is conflicting evidence in the literature on whether As(V) can be reduced to As(III) by iron filter media. This research uses electrochemical methods to investigate the redox reactions that occur on the surface of zerovalent iron in arsenic solutions. The effect of arsenic on the corrosion rate of zerovalent iron was investigated by analysis of Tafel diagrams for iron wire electrodes in anaerobic solutions with As(V) concentrations between 100 and 20,000 microg/L. As(V) reduction in the absence of surface oxides was investigated by analysis of chronoamperometry profiles for iron wire electrodes in solutions with As(V) concentrations ranging from 10000 to 106 microg/L. The effect of pH on As(V) reduction was investigated by analyses of chronopotentiometry profiles for iron wire electrodes at pH values of 2, 6.5, and 11. For freely corroding iron, the presence of As(III) and As(V) decreased the iron corrosion rate by a factor of 5 as compared to that in a 3 mM CaSO4 blank electrolyte solution. The decrease in corrosion rate was independent of the arsenic concentration and was due to the blocking of cathodic sites for water reduction by arsenic compounds chemisorbed to the iron surface. The chronoamperometry and chronopotentiometry experiments showed that elevated pH and increased As(III) to As(V) ratios near the iron surface decreased the thermodynamic favorability for As(V) reduction. Therefore, reduction of As(V) occurred only at potentials that were significantly below the apparent equilibrium potentials based on bulk solution pH values and As(III) to As(V) ratios. The potentials required to reduce more than 1% of the As(V) to As(III) were below those that are obtainable in freely corroding iron media. This indicates that there will be minimal or no reduction of As(V) in iron media filters under conditions relevant to potable water treatment.

摘要

零价铁屑已被提议作为一种过滤介质,用于从饮用水中去除As(III)和As(V)化合物。去除机制涉及亚砷酸盐和砷酸盐与铁表面以及铁腐蚀产生的铁氧化物形成络合物。关于铁过滤介质能否将As(V)还原为As(III),文献中有相互矛盾的证据。本研究采用电化学方法研究零价铁在砷溶液表面发生的氧化还原反应。通过分析As(V)浓度在100至20,000μg/L之间的厌氧溶液中铁丝电极的塔菲尔图,研究了砷对零价铁腐蚀速率的影响。通过分析As(V)浓度范围为10000至106μg/L的溶液中铁丝电极的计时电流曲线,研究了在无表面氧化物情况下As(V)的还原情况。通过分析pH值为2、6.5和11时铁丝电极的计时电位曲线,研究了pH对As(V)还原的影响。对于自由腐蚀的铁,与3 mM CaSO4空白电解质溶液相比,As(III)和As(V)的存在使铁的腐蚀速率降低了5倍。腐蚀速率的降低与砷浓度无关,是由于化学吸附在铁表面的砷化合物阻断了水还原的阴极部位。计时电流法和计时电位法实验表明,pH升高以及铁表面附近As(III)与As(V)的比例增加,降低了As(V)还原的热力学有利性。因此,As(V)的还原仅发生在明显低于基于本体溶液pH值和As(III)与As(V)比例的表观平衡电位的电位下。将超过1%的As(V)还原为As(III)所需的电位低于自由腐蚀铁介质中可获得的电位。这表明在与饮用水处理相关的条件下,铁介质过滤器中As(V)的还原将极少或不会发生。

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