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首页> 外文期刊>Geochimica et Cosmochimica Acta: Journal of the Geochemical Society and the Meteoritical Society >Synergistic effect of calcium and bicarbonate in enhancing arsenate release from ferrihydrite
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Synergistic effect of calcium and bicarbonate in enhancing arsenate release from ferrihydrite

机译:钙和碳酸氢根对增强亚铁从水铁矿中释放砷的协同作用

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Many groundwater systems contain anomalously high arsenic concentrations, associated with less than expected retention of As by adsorption to iron (hydr)oxides. Although carbonates are ubiquitous in aquifers, their relationship to arsenate mobilization is not well characterized. This research examines arsenate release from poorly crystalline iron hydroxides in abiotic systems containing calcium and magnesium with bicarbonate under conditions of static and dynamic flow (pH 7.5-8). Aqueous arsenic levels remained low when arsenate-bearing ferrihydrite was equilibrated with artificial groundwater solution containing Ca, Mg, and HCO_3~-. In batch titrations in which a solution of Ca and HCO_3~- was added repeatedly, the ferrihydrite surface became saturated with adsorbed Ca and HCO_3~-, and aqueous As levels increased by 1-2 orders of magnitude. In columns containing Ca or Mg and HCO_3~-, As solubility initially mimicked titrations, but then rapidly increased by an additional order of magnitude (reaching 12μM As). Separately, calcium chloride and other simple salts did not induce As release, although sodium bicarbonate and lactate facilitated minor As release under flow. Results indicate that adsorption of calcium or magnesium with bicarbonate leads to As desorption from ferrihydrite, to a degree greater than expected from competitive effects alone, especially under dynamic flow. This desorption may be an important mechanism of As mobilization in As-impacted, circumneutral aquifers, especially those undergoing rapid mineralization of organic matter, which induces calcite dissolution and the production of dissolved calcium and bicarbonate.
机译:许多地下水系统含有异常高的砷浓度,这与通过吸附到氧化铁(氢)中而保留的As少于预期的含量有关。虽然碳酸盐在含水层中无处不在,但它们与砷酸盐动员的关系尚不十分清楚。这项研究研究了在静态和动态流动(pH 7.5-8)条件下,含钙,镁和碳酸氢盐的非生物系统中结晶性较弱的氢氧化铁中砷的释放。当用含Ca,Mg和HCO 3〜-的人造地下水溶液平衡含砷三水铁矿时,含水砷水平仍然很低。在分批滴定法中,反复添加Ca和HCO_3〜-的溶液,亚铁酸盐表面被吸附的Ca和HCO_3〜-饱和,并且含水As含量增加了1-2个数量级。在含有Ca或Mg和HCO_3〜-的色谱柱中,As的溶解度最初类似于滴定,但随后又迅速增加了一个数量级(达到12μMAs)。单独地,尽管碳酸氢钠和乳酸盐在流动下促进了少量的As释放,但是氯化钙和其他简单的盐没有诱导As释放。结果表明,碳酸氢钙对钙或镁的吸附会导致砷从水铁矿中解吸,其程度要比单独竞争效应所预期的要大,尤其是在动态流动下。这种解吸可能是受砷影响的周围中性含水层中砷动员的重要机制,尤其是那些经历有机物快速矿化的水,这引起方解石溶解以及溶解的钙和碳酸氢盐的产生。

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