Field evaluation of in situ remediation of a heavy metal contaminated soil using lime and red-mud

We evaluated the effectiveness of lime and red mud (by-product of aluminium manufacturing) to reduce metal availability to Festuca rubra and to allow re-vegetation on a highly contaminated brown-field site. Application of both lime and red mud (at 3 or 5%) increased soil pH and decreased metal availability. Festuca rubra failed to establish in the control plots, but grew to a near complete vegetative cover on the amended plots. The most effective treatment in decreasing grass metal concentrations in the first year was 5% red mud, but by year two all amendments were equally effective. In an additional pot experiment, P application in combination with red mud or lime decreased the Pb concentration, but not total uptake of Pb in Festuca rubra compared to red mud alone. The results show that both red mud and lime can be used to remediate a heavily contaminated acid soil to allow re-vegetation.     

砷污染土壤柠檬酸萃取修复技术研究

伴随着砷工业的发展,含砷化学品引发的重大环境污染事故时有发生。一般砷污染事件发生后,土壤是其最直接的受害者,有必要寻找一种快速且行之有效的方法对砷污染土壤进行控制修复。针对此问题,通过实验探讨了柠檬酸萃取修复砷污染土壤的效果,研究了柠檬酸浓度、液土比、萃取时间及土壤共存离子对柠檬酸萃取砷的效果的影响,为砷污染土壤的治理提供依据。结果表明,柠檬酸是一种高效的砷萃取剂;随着柠檬酸浓度、液土比、萃取时间的增加,砷的萃取率均有所升高;当柠檬酸摩尔浓度为0.25 mol/L、液土比为20 mL/g、萃取时间为21 h时,柠檬酸对砷的萃取率达到最高值(70.58%);土壤中共存的PO43-、Zn2+、Fe2+,由于其竞争作用,能使柠檬酸对砷的萃取率降低。     

污染地下水原位处理方法:可渗透反应墙

可渗透反应墙法是 2 0世纪 90年代新兴的一种地下水污染原位处理方法 ,该方法目前在欧美已开始进入广泛的工程应用阶段。该方法与早期的一些处理方法相比 ,具有能持续原位处理、处理组分多、价格相对便宜等特点。本文系统介绍了该处理方法的基本原理、系统的结构构造和类型、处理机理和反应材料以及设计与施工等 ,为在我国开展该方法的研究和应用打下基础。     

污染地下水原位治理技术--透水性反应墙法

20世纪90年代初期在美国和加拿大兴起的原位被动修复技术--透水性反应墙,是一种地下水污染原位处理方法.其通过在垂直于地下水流动方向设置活性渗滤墙,当地下水流通过活性渗滤墙时,污染物与墙体材料发生化学反应,从而达到环境修复的目的.该技术具有原理简单,施工方便,能持续原位处理,处理组分多,且运行费用低廉等特点,能有效吸附和降解多种重金属和有机污染物.该方法目前在欧美已开始进入广泛的工程应用阶段,正逐步取代运行成本昂贵的抽水处理技术,成为地下水修复技术的发展方向.系统介绍了透水性反应墙法,阐述了反应墙的类型、活性材料的选取、反应机理、反应墙的构建以及应用实例,同时分析了其存在问题并展望其今后的研究方向.     

有机改性蒙脱石负载巯基修复汞污染土壤

以蒙脱石作为原始材料,对其进行有机改性,将巯基基团负载在有机改性的蒙脱石上制备出重金属汞的稳定剂以稳定化修复汞污染土壤。考察稳定化时间、稳定剂添加量、浸出液pH及有机质含量对稳定化效果的影响,探究稳定化前后土壤汞形态变化。通过XRD、FTIR和SEM分析了蒙脱石、有机改性蒙脱石（Mont-OR）和负载巯基有机改性蒙脱石（Mont-OR-SH）的物理化学特征,通过原子吸收法测定汞浓度。稳定化修复结果表明,稳定化时间为30 d,稳定剂添加量为9%时,汞浸出浓度为0.066 mg·L-1,稳定率为98.3%,达到GB 5085.3-2007规定的汞限值0.10 mg·L-1。添加不同质量的小麦秸秆作为有机质的来源,均对整个稳定化有促进作用,其中添加量为6%时,促进作用最明显,改变浸出液pH,在强酸性和强碱性条件下,利用此稳定剂对汞的稳定作用降低。TESSIER五步提取法结果表明,负载巯基的有机改性蒙脱石的添加导致可交换态汞、碳酸盐结合态汞、铁锰氧化物结合态汞含量下降,而有机结合态汞、残渣态汞含量增加。实验结果证明有机改性蒙脱石负载巯基能够有效地应用于汞污染土壤修复。     

粘土矿物修复重金属污染土壤

简要介绍了我国土壤重金属污染的现状与危害.通过粘土矿物在重金属污染土壤中净化功能的阐述,提出利用粘土矿物修复土壤重金属污染的观点.继而从天然和改性粘土矿物特性,叙述了粘土矿物修复土壤重金属污染的机制与应用进展及其影响因素.最后讨论了粘土矿物在修复土壤重金属污染过程中值得注意的几个问题,并展望了粘土矿物在该领域应用中的发展方向.     

腐殖质纳米颗粒对镉污染土壤的修复

外源腐殖质可改变土壤镉（Cd）的含量和状态。以风化煤为原料制备的不溶性胡敏酸为吸附剂,对比研究了其对冶炼厂周边污染土壤及人工模拟污染土壤中Cd的钝化效果。再以泥炭为原料,制备富里酸钾为主的水溶性腐殖酸钾为淋洗剂,用于活化、去除上述2种土壤中的Cd。结果表明,胡敏酸在砂质的人工模拟污染土壤中钝化效果更好,2%的剂量可使土壤中CaCl2提取态Cd的浓度（0.103 mg·L-1）降低19.7%。腐殖酸钾去除土壤Cd的效率随淋洗剂浓度增加而提高,在10 g·L-1的浓度时,单次淋洗可去除高达38.1%的Cd。傅里叶变换红外光谱分析表明,腐殖质与Cd反应后形成了羧酸盐。因此,腐殖质纳米颗粒既可以钝化土壤中的Cd,也可以活化土壤中的Cd,从而达到修复Cd污染土壤的目的。其关键在于根据钝化或活化的目标,选择溶解度适当的腐殖质材料。     

Kinetic constraints on theIn-situ remediation of soils contaminated with organic chemicals

Cleanup of contaminated soils to comply with soil quality limits currently receives much interest.In-situ remediation of contaminated soils relies on the ability of the techniques employed to enhance the rate of release of contaminants from the soil-sorbed and nonaqueous phase liquid (NAPL) phases into the aqueous or gaseous phases from which they can be more readily removed and treated. Contaminant concentrations in these “environmentally mobile” forms usually decline over time so that the economic efficiency and the overall success of remediation technologies are subject to the “law of diminishing returns”. In this paper we consider the “state of the art” in our understanding of NAPL dissolution and transport, desorption of soilsorbed contaminants and fluid flow in porous media. The extent to which these processes may constrain the success of bioremediation, pump-and-treat remediation and soil venting in relation to established soil quality limits is addressed. Finally, we suggest directions for future research and comment on legislative considerations.     

铜污染场地土壤的原位电动强化修复

电动修复技术是一种新型的污染土壤修复技术,相关的理论和实验室小试研究较多,但鲜见野外现场条件下的原位修复研究。本研究以某电镀厂铜污染区为修复对象,以可生物降解的络合剂乳酸和柠檬酸为阴极池增强试剂,考察在原位条件下电动修复技术对土壤中铜的去除效率,并评估修复过程的电能消耗。结果表明:在电压梯度7.5 V·m-1,阴极池乳酸和柠檬酸浓度为0.5 mol·L-1,处理24 d(乳酸处理)和17 d(柠檬酸处理)的条件下,乳酸处理较柠檬酸处理电流要高、且阴阳极池溶液和土壤的pH、电导率变化要小;乳酸处理后土壤铜含量明显下降(阳极和阴极附近土壤铜去除率分别为52.6%和35.7%),而柠檬酸处理条件下阳极和阴极附近铜的去除效率分别为27.2%和-17.5%,这可能与其较低的电流和较短的处理时间有关。与现有文献比较,乳酸处理总能耗(15.7 kWh·m-3)处于较低水平,而Cu的去除率处于较高水平(35.7%~52.6%),优于文献报道的电动修复去除效率和电能消耗。     

污染土壤化学修复技术研究与进展

污染土壤修复环境工程近年来发展迅猛，欧美等发达国家在其技术创新和设备改进2个层面都取得了长足进展。本文概述了化学淋洗修复技术（原位化学修复技术和异位化学修复技术）、化学还原与还原脱氯修复技术、化学氧化修复技术、溶剂浸提技术和土壤性能化学改良修复技术等污染土壤的化学修复技术原理、进展与适用性以及有关关键技术参数，并对其发展前景进行了展望。     

Modeling EDTA enhanced electrokinetic remediation of lead contaminated soils

Electrokinetic extraction has been tested for lead removal from Algerian contaminated soils. For this purpose, a chelating reagent (EDTA, 0.1M) has been injected into the catholyte. This procedure is expected to enhance the process by desorption of the contaminant and formation of new mobile species negatively charged. A mathematical model based on Nernst-Planck theory has also been developed to predict the evolution of lead distribution across the soil as a function of time. The results of several experiments carried out on various duration (10, 20 and 40 days) have shown the importance on treatment efficiency of pollution age and contaminant speciation as determined by sequential chemical extraction.     

Optimizing the molarity of a EDTA washing solution for saturated-soil remediation of trace metal contaminated soils

Three experiments were conducted to optimize the use of ethylenediaminetetraacetic acid (EDTA) for reclaiming urban soils contaminated with trace metals. As compared to Na(2)EDTA, (NH(4))(2)EDTA extracted 60% more Zn and equivalent amounts of Cd, Cu and Pb from a sandy loam. When successively saturating and draining loamy sand columns during a washing cycle, which submerged it once with a (NH(4))(2)EDTA wash and four times with deionised water, the post-wash rinses largely contributed to the total cumulative extraction of Cd, Co, Cr, Cu, Mn, Ni, Pb and Zn. Both the washing solution and the deionised water rinses were added in a 2:5 liquid to soil (L:S) weight ratio. For equal amounts of EDTA, concentrating the washing solution and applying it and the ensuing rinses in a smaller 1:5 L:S weight ratio, instead of a 2:5 L:S weight ratio, increased the extraction of targeted Cr, Cu, Ni, Pb and Zn.     

表面活性剂增效修复土壤有机污染研究进展

系统评述了表面活性剂增效修复土壤有机污染的原理、研究现状及存在的问题。     

污染土壤化学修复技术研究与进展

污染土壤修复环境工程近年来发展迅猛,欧美等发达国家在其技术创新和设备改进2个层面都取得了长足进展。本文概述了化学淋洗修复技术(原位化学修复技术和异位化学修复技术)、化学还原与还原脱氯修复技术、化学氧化修复技术、溶剂浸提技术和土壤性能化学改良修复技术等污染土壤的化学修复技术原理、进展与适用性以及有关关键技术参数,并对其发展前景进行了展望。     

表面活性剂增效修复土壤有机污染研究进展

系统评述了表面活性剂增效修复土壤有机污染的原理、研究现状及存在的问题.     

Efficacy of in-situ for the remediation of PAH contaminated soils

Polycyclic aromatic hydrocarbons (PAHs) are of environmental concern because many PAHs are either carcinogens or potential carcinogens. Petroleum products are a major source of PAHs. The occurrence of PAH contamination is widespread and novel treatment technologies for the remediation of contaminated soils are necessary.Ozone has been found to be extremely useful for the degradation of PAHs in soils. For these compounds, the reaction with molecular ozone appears to be the more important degradation pathway. Greater than 95% removal of phenanthrene was achieved with an ozonation time of 2.3 h at an ozone flux of 250 mg h⁻¹. After 4.0 h of treatment at an ozone flux of 600 mg h⁻¹, 91 % of the pyrene was removed. We have also found that the more hydrophobic PAHs (e.g. chrysene) react more slowly than would be expected on the basis of their reactivity with ozone, suggesting that partitioning of the contaminant into soil organic matter may reduce the reactivity of the compound. Even so, after 4 h of exposure to ozone, the chrysene concentration in a contaminated Metea soil was reduced from 100 to 50 mg kg⁻¹ .Ozone has been found to be readily transported through columns packed with a number of geological materials, including Ottawa sand, Metea soil, Borden aquifer material and Wurtsmith aquifer material. All of these geological materials exerted a limited (finite) ozone demand, i.e. the rate of ozone degradation in soil columns is very slow after the ozone demand is met. Moisture content was found to increase the ozone demand, most likely owing to the dissolution of gaseous ozone into the pore water. As once the initial ozone demand is met, little degradation of ozone is observed, it should be possible to achieve ozone penetration to a considerable distance away from the injection well, suggesting that in-situ ozonation is a feasible means of treating uncontaminated unsaturated soils. This is substantiated by two field studies where in-situ ozonation was apparently successful at remediating the sites.     

电动力学法修复土壤环境重金属污染的研究进展

介绍了电动力学法的基本原理和国外的一些电动力学修复重金属污染土壤的工艺,如Lasagna工艺、阴极区注导电性溶液工艺、阳离子选择性透过膜、CEHIXM工艺、Electro—Klean^TM电分离技术、电化学自然氧化技术、电化学离子交换技术、电吸附技术等,并指出了这些工艺的优缺点。评价了电动力学法处理地下土壤环境中重金属污染的优势及目前存在的问题。     

生石灰强化机械通风法修复三氯乙烯污染土壤

机械通风法是一种操作简单、效果好、成本低的土壤修复技术,特别适合大型挥发性有机化合物(VOC)污染场地的土壤修复,但在环境温度低、土壤含水率高、土壤黏性大等情况下,其修复效果和修复周期会受到极大影响,且土壤中高浓度的污染物残留将严重影响场地修复目标的实现。为了解决这一问题,采用了在土壤中添加一定量生石灰的强化措施。结果表明:(1)生石灰可以显著提高机械通风法修复三氯乙烯(TCE)污染土壤的效果,缩短修复周期,降低污染物在土壤中的残留浓度。(2)生石灰对TCE的强化作用与生石灰的添加量和土壤类型有关,粉质黏土的强化效果要好于粉土和细砂,生石灰添加量越多,强化效果越好;(3)生石灰强化处理TCE的主要机制是提高土壤温度、降低土壤含水率、增加土壤通透性,促进土壤中TCE的解吸和挥发。     

Biosurfactant technology for remediation of cadmium and lead contaminated soils

This research focuses on column experiments conducted to evaluate the potential of environmentally compatible rhamnolipid biosurfactant produced by Pseudomonas aeruginosa strain BS2 to remove heavy metals (Cd and Pb) from artificially contaminated soil. Results have shown that di-rhamnolipid removes not only the leachable or available fraction of Cd and Pb but also the bound metals as compared to tap water which removed the mobile fraction only. Washing of contaminated soil with tap water revealed that approximately 2.7% of Cd and 9.8% of Pb in contaminated soil was in freely available or weakly bound forms whereas washing with rhamnolipid removed 92% of Cd and 88% of Pb after 36 h of leaching. This indicated that di-rhamnolipid selectively favours mobilization of metals in the order of Cd>Pb. Biosurfactant specificity observed towards specific metal will help in preferential elution of specific contaminant using di-rhamnolipid. It was further observed that pH of the leachates collected from heavy metal contaminated soil column treated with di-rhamnolipid solution was low (6.60-6.78) as compared to that of leachates from heavy metal contaminated soil column treated with tap water (pH 6.90-7.25), which showed high dissolution of metal species from the contaminated soil and effective leaching of metals with treatment with biosurfactant. The microbial population of the contaminated soil was increased after removal of metals by biosurfactant indicating the decrease of toxicity of metals to soil microflora. This study shows that biosurfactant technology can be an effective and nondestructive method for bioremediation of cadmium and lead contaminated soil.     

鼠李糖脂与菌剂对原油污染土壤的联合修复

为研究RL强化MI修复原油污染土壤的效果,通过盆栽实验,测定了修复过程中微生物、脱氢酶、原油降解率和正构烷烃等变化.结果表明,提取RL具有良好表面和乳化活性.修复过程中微生物数目、脱氢酶和石油降解率具有相关性.RL+MI联合修复对原油的降解效果最显著,第14、21和28天的降解率分别达67.6%、78.6%和81.3%,较MI和RL处理分别提高了22%~24%和32%~38%;细菌、放线菌和霉菌最高生物量分别比CK提高约20、5.8和4.7倍;GC-MS示修复14 d后∑C21-/∑C22+(1.334)和Pr/Ph(1.152)均大于CK,说明降解早期具有高碳正构烷烃、奇数烷烃的降解优势以及对类异戊二烯烷烃的降解.