Liang Chenju, Bruell Clifford J, Marley Michael C, Sperry Kenneth L
Department of Civil and Environmental Engineering, University of Massachusetts, One University Avenue, Lowell, MA 01854, USA.
Chemosphere. 2004 Jun;55(9):1225-33. doi: 10.1016/j.chemosphere.2004.01.030.
In situ chemical oxidation (ISCO) is a technique used to remediate contaminated soil and groundwater systems. It has been postulated that sodium persulfate (Na2S2O8) can be activated by transition metal ions such as ferrous ion (Fe2+) to produce a powerful oxidant known as the sulfate free radical (SO4-*) with a redox potential of 2.6 V, which can potentially destroy organic contaminants. In this laboratory study persulfate oxidation of dissolved trichloroethylene (TCE) was investigated in aqueous and soil slurry systems under a variety of experimental conditions. A chelating agent (i.e., citric acid) was used in attempt to manipulate the quantity of ferrous ion in solution by providing an appropriate chelate/Fe2+ molar ratio. In an aqueous system a chelate/Fe2+ molar ratio of 1/5 (e.g., S2O8(2)-/chelate/Fe2+/TCE ratio of 20/2/10/1) was found to be the lowest acceptable ratio to maintain sufficient quantities of Fe2+ activator in solution resulting in nearly complete TCE destruction after only 20 min. The availability of Fe2+ appeared to be controlled by adjusting the molar ratio of chelate/Fe2+. In general, high levels of chelated ferrous ion concentrations resulted in faster TCE degradation and more persulfate decomposition. However, if initial ferrous ion contents are relatively low, sufficient quantities of chelate must be provided to ensure the chelation of a greater percentage of the limited ferrous ion present. Citric acid chelated ferrous ion appeared effective for TCE degradation within soil slurries but required longer reaction times. Additionally, the use of citric acid without the addition of supplemental Fe2+ in soil slurries, where the citric acid apparently extracted native metals from the soil, appeared to be somewhat effective at enhancing persulfate oxidation of TCE over extended reaction times. A comparison of different chelating agents revealed that citric acid was the most effective.
原位化学氧化(ISCO)是一种用于修复受污染土壤和地下水系统的技术。据推测,过硫酸钠(Na2S2O8)可被亚铁离子(Fe2+)等过渡金属离子活化,生成一种氧化还原电位为2.6 V的强氧化剂——硫酸根自由基(SO4-*),它有可能破坏有机污染物。在本实验室研究中,在各种实验条件下,对水相和土壤浆液系统中溶解的三氯乙烯(TCE)的过硫酸盐氧化进行了研究。使用了一种螯合剂(即柠檬酸),试图通过提供合适的螯合剂/Fe2+摩尔比来控制溶液中亚铁离子的量。在水相系统中,发现螯合剂/Fe2+摩尔比为1/5(例如,S2O8(2)-/螯合剂/Fe2+/TCE比例为20/2/10/1)是维持溶液中足够量的Fe2+活化剂的最低可接受比例,仅20分钟后就能使TCE几乎完全降解。Fe2+的有效性似乎通过调节螯合剂/Fe2+的摩尔比来控制。一般来说,高浓度的螯合亚铁离子会导致TCE降解更快,过硫酸盐分解更多。然而,如果初始亚铁离子含量相对较低,则必须提供足够量的螯合剂,以确保螯合更多比例的有限亚铁离子。柠檬酸螯合亚铁离子在土壤浆液中对TCE降解似乎有效,但需要更长的反应时间。此外,在土壤浆液中使用不添加补充Fe2+的柠檬酸,柠檬酸显然从土壤中提取了天然金属,在延长的反应时间内,对增强TCE的过硫酸盐氧化似乎有一定效果。不同螯合剂的比较表明,柠檬酸是最有效的。