Gómez J, Alcántara M T, Pazos M, Sanromán M A
Department of Chemical Engineering, University of Vigo, E-36310 Vigo, Spain.
Chemosphere. 2009 Mar;74(11):1516-21. doi: 10.1016/j.chemosphere.2008.11.019. Epub 2008 Dec 17.
An innovative process that combines soil electrokinetic remediation and liquid electrochemical oxidation for the degradation of organic compounds present in a polluted soil was developed and evaluated by using benzo[a]pyrene spiked kaolin. In order to increase benzo[a]pyrene solubility during electrokinetic treatment, the addition of a co-solvent or surfactant, such as ethanol or Brij 35, as flushing solution was tested. The research carried out demonstrated the influence of the desorption agent employed on benzo[a]pyrene remediation from the kaolin matrix. Thus, if the flushing solution was ethanol at 40%, there was no presence of contaminant in either chamber. On the contrary, when a solution of surfactant Brij 35 was used, benzo[a]pyrene was transported towards the cathode chamber, where it was collected. Moreover, the extent of this recovery depends on the pH profile on the soil. When no pH control was used, around 17% of initial contaminant was detected in the cathode chamber; however, when pH control was applied, the recovery of benzo[a]pyrene could be higher than 76%, when the pH control in the anode chamber was set at 7.0. In order to obtain the total degradation of mobilised benzo[a]pyrene from the contaminated soil, the liquid collected by electrokinetic remediation was oxidised by electrochemical treatment. This oxidation was accomplished via an electrochemical cell with a working volume of 0.4 L, and graphite as electrode material. The benzo[a]pyrene was almost totally degraded in 1d, reaching a degradation of about 73% in 16 h.
开发了一种创新工艺,该工艺将土壤电动修复与液体电化学氧化相结合,用于降解污染土壤中存在的有机化合物,并使用苯并[a]芘加标的高岭土进行了评估。为了在电动处理过程中提高苯并[a]芘的溶解度,测试了添加共溶剂或表面活性剂(如乙醇或Brij 35)作为冲洗液的效果。所开展的研究证明了所用解吸剂对高岭土基质中苯并[a]芘修复的影响。因此,如果冲洗液为40%的乙醇,则两个腔室中均不存在污染物。相反,当使用表面活性剂Brij 35溶液时,苯并[a]芘向阴极室迁移并在那里被收集。此外,这种回收程度取决于土壤的pH分布。当不进行pH控制时,在阴极室中检测到约17%的初始污染物;然而,当进行pH控制时,将阳极室的pH控制设置为7.0时,苯并[a]芘的回收率可能高于76%。为了使污染土壤中迁移出的苯并[a]芘完全降解,通过电化学处理将电动修复收集的液体进行氧化。这种氧化通过一个工作体积为0.4 L、以石墨为电极材料的电化学池来完成。苯并[a]芘在1天内几乎完全降解,在16小时内降解率达到约73%。