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Simultaneous removal of organic compounds and heavy metals from soils by electrokinetic remediation with a modified cyclodextrin

机译:通过修饰环糊精的电动修复同时去除土壤中的有机化合物和重金属

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Thousands of sites are contaminated with both heavy metals and organic compounds and these sites pose a major threat to public health and the environment. Previous studies have shown that electrokinetic remediation has potential to remove heavy metals and organic compounds when they exist individually in low permeability soils. This paper presents the feasibility of using cyclodextrins in electrokinetic remediation for the simultaneous removal of heavy metals and polycyclic aromatic hydrocarbons (PAHs) from low permeability soils. Kaolin was selected as a model low permeability soil and it was spiked with phenanthrene as well as nickel at concentrations of 500 mg kg~(-1) each to simulate typical mixed field contamination. Bench-scale electrokinetic experiments were conducted using hydroxypropyl β-cyclo-dextrin (HPCD) at low (1%) and high (10%) concentrations and using deionized water in control test. A periodic voltage gradient of 2 VDC cm~(-1) (with 5 d on and 2 d off) was applied to all the tests, and 0.01 M NaOH was added during the experiments to maintain neutral pH conditions at anode. In all tests, nickel migrated as Ni~(2+) ions towards the cathode and most of it was precipitated as Ni(OH)_2 within the soil close to the cathode due to high pH condition generated by electrolysis reaction. The solubility of phenanthrene in the flushing solution and the amount of electroosmotic flow controlled the migration and removal of phenanthrene in all the tests. Even though high flow was generated in tests using deionized water and 1% HPCD, migration and removal of phenanthrene was low due to low solubility of phenanthrene in these solutions. The test with 10% HPCD solution showed higher solubility of phenanthrene which caused it migrate towards the cathode, but further migration and removal was retarded due to reduced electric current and electroosmotic flow. Approximately one pore volume of flushing resulted in approximately 50% removal of phenanthrene from the soil near the anode. Sustained higher electroosmotic flow with higher concentration cyclodextrin and maintaining low soil pH near cathode should be investigated to increase removal efficiency of both phenanthrene and nickel.
机译:数以千计的场所都被重金属和有机化合物污染,这些场所对公共卫生和环境构成了重大威胁。以前的研究表明,电动修复具有潜力,当重金属和有机化合物单独存在于低渗透性土壤中时,可以去除它们。本文介绍了使用环糊精电动修复同时从低渗透性土壤中去除重金属和多环芳烃(PAHs)的可行性。高岭土被选为典型的低渗透性土壤,并掺有菲和镍,每种浓度为500 mg kg〜(-1),以模拟典型的混合田污染。在低浓度(1%)和高浓度(10%)下,使用羟丙基β-环糊精(HPCD),并在对照试验中使用去离子水,进行了台式电动实验。在所有测试中均采用2 VDC cm〜(-1)的周期性电压梯度(开启5 d和关闭2 d),并在实验过程中添加0.01 M NaOH以保持阳极的中性pH条件。在所有测试中,由于电解反应产生的高pH条件,镍以Ni〜(2+)离子的形式向阴极迁移,并且大部分以Ni(OH)_2的形式沉淀在靠近阴极的土壤中。在所有测试中,菲在冲洗溶液中的溶解度和电渗流量控制着菲的迁移和去除。即使在使用去离子水和1%HPCD的测试中产生了高流量,但是由于菲在这些溶液中的溶解度低,所以菲的迁移和去除仍然很低。用10%HPCD溶液进行的测试表明,菲具有较高的溶解度,导致其向阴极迁移,但由于电流和电渗流减少,进一步的迁移和去除受到了阻碍。大约一孔的冲洗量导致从阳极附近的土壤中除去大约50%的菲。为了提高菲和镍的去除效率,应研究使用较高浓度的环糊精维持较高的电渗流并在阴极附近保持较低的土壤pH。

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