Pociecha Maja, Lestan Domen
Agronomy Department, Biotechnical Faculty, University of Ljubljana, Ljubljana, Slovenia.
J Hazard Mater. 2009 Jun 15;165(1-3):533-9. doi: 10.1016/j.jhazmat.2008.10.006. Epub 2008 Oct 14.
The feasibility of a two-phase method for remediation of Cu (364+/-2 mg kg(-1)) contaminated vineyard soil was evaluated. In the first phase we used ethylenediamine tetraacetae (EDTA) for Cu leaching, while in the second phase we used an electrochemical advanced oxidation process (EAOP) for the treatment and reuse of the washing solution for soil rinsing (removal of soil-retained, chelant-mobilized Cu complexes) in a closed loop. In the EAOP, a boron-doped diamond anode was used for the generation of hydroxyl radicals and oxidative decomposition of EDTA-metal complexes at a constant current density (40 mA cm(-2)). The released Cu was removed from the solution mostly as an electro-deposit on the cathode. Two consecutive additions of 10 mmol kg(-1) EDTA removed 26% of Cu from the soil, mostly from carbonate and oxide soil fractions (58% and 40% Cu reduction). The soil Cu oral availability (in vitro Physiologically Based Extraction Test) was reduced after remediation by 42% and 51% in the simulated stomach and intestinal phases. The discharge solution was clear, almost colorless, with pH 8.4 and 0.5 mg L(-1) Cu and 0.07 mM EDTA. The novel method enables soil Cu availability stripping using small volumes of process waters, and no wastewater generation or other emissions into the environment.
评估了一种用于修复铜(364±2毫克/千克)污染葡萄园土壤的两相法的可行性。在第一阶段,我们使用乙二胺四乙酸(EDTA)进行铜的淋洗,而在第二阶段,我们使用电化学高级氧化工艺(EAOP)处理并回用洗涤液,以在闭环中对土壤进行冲洗(去除土壤中保留的、螯合剂活化的铜络合物)。在EAOP中,使用掺硼金刚石阳极在恒定电流密度(40毫安/平方厘米)下产生羟基自由基并氧化分解EDTA-金属络合物。释放出的铜大部分以电沉积物的形式在阴极从溶液中去除。两次连续添加10毫摩尔/千克的EDTA从土壤中去除了26%的铜,大部分来自碳酸盐和氧化物土壤组分(铜减少58%和40%)。修复后,土壤铜的口服可利用性(体外基于生理学的提取试验)在模拟胃和肠道阶段分别降低了42%和51%。排放溶液清澈,几乎无色,pH值为8.4,铜含量为0.5毫克/升,EDTA含量为0.07毫摩尔/升。该新方法能够使用少量工艺用水去除土壤中的铜可利用性,且不产生废水或向环境排放其他污染物。