Yang Jung-Seok, Kwon Man Jae, Choi Jaeyoung, Baek Kitae, O'Loughlin Edward J
Korea Institute of Science and Technology (KIST) - Gangneung Institute, Gangneung 210-340, Republic of Korea.
Korea Institute of Science and Technology (KIST) - Gangneung Institute, Gangneung 210-340, Republic of Korea.
Chemosphere. 2014 Dec;117:79-86. doi: 10.1016/j.chemosphere.2014.05.079. Epub 2014 Jun 25.
Electrokinetic remediation (also known as electrokinetics) is a promising technology for removing metals from fine-grained soils. However, few studies have been conducted regarding the transport behavior of multi-metals during electrokinetics. We investigated the transport of As, Cu, Pb, and Zn from soils during electrokinetics, the metal fractionation before and after electrokinetics, the relationships between metal transport and fractionation, and the effects of electrolyte conditioning. The main transport mechanisms of the metals were electroosmosis and electromigration during the first two weeks and electromigration during the following weeks. The direction of electroosmotic flow was from the anode to the cathode, and the metals in the dissolved and reducible-oxides fractions were transported to the anode or cathode by electromigration according to the chemical speciation of the metal ions in the pore water. Moreover, a portion of the metals that were initially in the residual fraction transitioned to the reducible and soluble fractions during electrokinetic treatment. However, this alteration was slow and resulted in decreasing metal removal rates as the electrokinetic treatment progressed. In addition, the use of NaOH, H3PO4, and Na2SO4 as electrolytes resulted in conditions that favored the precipitation of metal hydroxides, phosphates, and sulfates in the soil. These results demonstrated that metal removal was affected by the initial metal fractionation, metal speciation in the pore solution, and the physical-chemical parameters of the electrolytes, such as pH and electrolyte composition. Therefore, the treatment time, use of chemicals, and energy consumption could be reduced by optimizing pretreatment and by choosing appropriate electrolytes for the target metals.
电动修复(也称为电动动力学)是一种从细粒土壤中去除金属的很有前景的技术。然而,关于电动动力学过程中多金属的迁移行为的研究很少。我们研究了电动动力学过程中土壤中砷、铜、铅和锌的迁移、电动动力学前后金属的分级、金属迁移与分级之间的关系以及电解质调节的影响。在前两周,金属的主要迁移机制是电渗和电迁移,在接下来的几周是电迁移。电渗流方向是从阳极到阴极,溶解态和可还原氧化物态的金属根据孔隙水中金属离子的化学形态通过电迁移被输送到阳极或阴极。此外,一部分最初处于残留态的金属在电动修复处理过程中转变为可还原态和可溶态。然而,这种变化很缓慢,并且随着电动修复处理的进行导致金属去除率下降。此外,使用氢氧化钠、磷酸和硫酸钠作为电解质会导致有利于土壤中金属氢氧化物、磷酸盐和硫酸盐沉淀的条件。这些结果表明,金属去除受到初始金属分级、孔隙溶液中金属形态以及电解质的物理化学参数(如pH值和电解质组成)的影响。因此,通过优化预处理并为目标金属选择合适的电解质,可以减少处理时间、化学品使用量和能源消耗。