可渗透反应复合电极法对土壤重金属的电动去除

将零价铁(Fe0)、沸石等活性材料附着在电极上形成可渗透反应层并构成可渗透反应复合电极,采用不同的复合电极对Cd2+、Ni 2+、Pb2+和Cu2+等4种阳离子型重金属污染土壤进行了电动力学修复。研究了不同可渗透反应复合电极对土壤pH的控制效果以及对重金属的去除作用,分析了迁移到复合电极中的重金属形态变化。结果表明,复合电极中添加酸、碱性沸石并适时更换,可有效中和、截留阴阳极电解产生的OH-和H+,避免或减缓土壤酸碱迁移带的形成,防止重金属离子的过早沉淀及土壤过度酸化,极大提高了重金属的去除率。复合电极中Fe0可将迁移进来的重金属离子进行还原稳定,实现重金属污染物的捕获与固定,与迁移到沸石复合电极中的4种重金属不稳定态相比,"Fe0+沸石"复合电极中重金属不稳定态分别下降了61.4、60.5、61.4、57.1百分点。结果还显示,阴极采用"Fe0+沸石"复合电极并适时进行更换,施加1.5V/cm的直流电压修复10d后,土壤中Cd、Ni、Pb、Cu的总去除率分别为44.5%、41.5%、33.5%和36.7%,且进一步延长修复时间和持续更换电极可获得更为理想的修复效果。     

改良剂对重金属复合污染土壤的修复效果

为揭示不同改良剂及其联合施用对重金属复合污染土壤的修复效果,采用室内土壤培养实验和室外盆栽实验相结合,研究不同施用量(10和20 g·kg~(-1))的蛭石(A)、泥炭(B)和骨粉(C)以及两两组合施用下,改良剂对土壤重金属DT-PA有效态、植物(以空心菜为例)生物量、株高以及植物可食部重金属含量的影响。结果表明:不同处理条件下的土壤p H值的提升与空白对照相比变化不显著;单施2%泥炭对土壤重金属Cu、Zn的钝化效果优于其他处理组,相对空白对照组,在第42天2种金属有效态含量分别降低了57.65%和65.55%,而1%蛭石和1%骨粉的混合添加能有效降低土壤中有效态Cd含量,相对空白对照组在第42天有效态Cd含量降低了40.52%;3种改良剂单施和混施对空心菜均具有增产增收的显著效果,且混施改良剂对空心菜增产效果较好;各处理组中空心菜体内Cu、Zn和Cd含量均有显著的降低,其中2%泥炭、1%蛭石+1%泥炭和1%蛭石+1%骨粉处理组分别对空心菜体内Cu、Zn和Cd含量降低效果最好,相对空白对照组分别降低了75.39%、70.75%和75.42%。因此,在该污染类型土壤泥炭、蛭石+泥炭和蛭石+骨粉分别对空心菜吸收土壤中的Cu、Zn和Cd具有较好的阻控效果。     

贵阳南部近郊蔬菜重金属污染状况及健康风险评估

于贵阳花溪区蔬菜种植基地及零星菜地采集叶菜类、茎菜类和果菜类样品及对应土壤样品,测定土壤与蔬菜样品中Zn、Cd、Pb和Cu含量,分析土壤理化性质、土壤重金属全量、有效态含量与蔬菜中重金属含量之间的关系,通过污染指数和暴露风险健康评估指数分析城郊蔬菜中重金属污染状况以及摄入人群的健康风险。结果表明:部分菜地土壤样品Zn、Cu含量超出农用地土壤污染风险筛选值,超标率分别为8.82%、11.76%;蔬菜中重金属含量主要取决于土壤重金属有效态含量;研究区蔬菜均处于清洁水平,但有8.82%的蔬菜样品Pb处于Ⅱ级警戒值,且均为叶菜;Pb是叶菜类暴露健康风险的主要元素,而Cu是茎菜类与果菜类暴露健康风险的重要元素;蔬菜重金属对儿童和成人的危害指数均小于1.0,表明食用该地区的蔬菜不会对人体健康产生不良影响。     

重金属离子Cd^2＋、Pb^2＋污染对土壤酶活性的影响

通过对土壤中比较重要的两种酶（过氧化氢酶、脲酶）活性的测定,研究了重金属离子（Cd^2＋、Pb^2＋）单因素污染、复合污染对两种酶活性的影响,进而找出重金属污染程度与土壤酶活性的关系,为建立土壤中的酶活性可以表征重金属污染程度的生化指标平台提供试验依据。结果表明,在Cd^2＋、Pb^2＋单因素污染影响中,在一定浓度下的重金属离子对土壤酶活性会有激活效应,但大多表现为抑制效应;Cd^2＋、Pb^2＋复合污染对两种土壤酶活性的影响存在着明显差异,其复合污染对脲酶表现出协同抑制负效应的特征;对过氧化氢酶表现出一定的屏蔽作用。通过重金属离子形态对土壤酶有效性影响的研究,脲酶活性可以作为土壤重金属离子（Cd^2＋、Pb^2＋）单因素和复合污染程度的主要生化指标。     

土壤及土壤-植物系统中复合污染的研究进展

土壤复合污染是土壤污染的主要存在形式，在分析中，主要从土壤重金属复合污染和土壤重金属-有机污染物复合污染方面进行了较为全面的综述，评价了土壤复合污染的多种表征方法，并且讨论了该研究当前仍存在的一些问题。     

磷改性生物炭对Pb、Cd复合污染土壤的钝化效果

中国存在着较大面积受重金属污染土壤,尤其是Pb、Cd两种重金属的复合污染较常见。利用磷改性生物炭对Pb、Cd复合污染土壤展开修复研究。结果表明:(1)磷改性生物炭可使土壤中Pb、Cd由弱酸提取态向可氧化态、残渣态转变,Pb的可氧化态和残渣态分别增加了19.4、16.9百分点,Cd的可氧化态、残渣态分别增加了17.4、9.9百分点;(2)磷改性生物炭可提高土壤有效磷,有效磷最终稳定在39 mg/kg左右;(3)磷改性生物炭能显著增加土壤阳离子交换量至19.3 cmol/kg。磷改性生物炭不仅能有效钝化重金属,还能有效改善土壤质量。     

重金属-多氯联苯复合污染土壤同步洗脱

电子垃圾拆解区土壤具有重金属与有机物复合污染的特性,尤其以Cu、Pb、Cd和多氯联苯(PCBs)的复合污染较为突出。为了同步脱除土壤中重金属与PCBs,选用增溶物质:Tween 80、TX-100、SDBS、β-环糊精与螯合剂柠檬酸依次组合进行复合污染土壤淋洗实验,应用批量平衡震荡法研究它们对重金属(Cu、Pb、Cd)与PCBs(Aroclor 1254)的洗脱效果。通过比较洗脱效果、环境友好性等方面,得出非离子表面活性剂Tween 80与天然螯合剂柠檬酸2种淋洗剂复合最佳;进一步研究两者的淋洗先后顺序、浓度配比、洗脱时间及淋洗剂p H对污染土壤洗脱效果的影响,结果表明,在Tween 80和柠檬酸均为10 g/L、p H=6、淋洗时间12 h时淋洗效果达到最佳,对Cu、Pb、Cd及PCBs的洗脱率分别达到98.77%、55.92%、66.82%和58.01%。因此,利用Tween80和柠檬酸组合可同时有效去除土壤重金属和PCBs,是复合污染土壤淋洗修复的有效淋洗剂。     

土壤及土壤-植物系统中复合污染的研究进展

土壤复合污染是土壤污染的主要存在形式 ,在分析中 ,主要从土壤重金属复合污染和土壤重金属 有机污染物复合污染方面进行了较为全面的综述 ,评价了土壤复合污染的多种表征方法 ,并且讨论了该研究当前仍存在的一些问题     

发酵鸡粪和有机磷肥对土壤中Pb、Cd污染的影响

研究了湘西地区常用的发酵鸡粪和有机磷肥施用对不同程度Pb、Cd复合污染土壤中乙三胺五醋酸(DTPA)提取态Pb(DTPA-Pb)、DTPA提取态Cd(DTPA-Cd)和土壤酶的影响,并研究了对于种植黑麦草(Lolium perenne L.)的影响。结果表明:(1)施用发酵鸡粪和有机磷肥均能显著改善土壤酸性,一定程度上提高土壤有机质含量。在加入质量浓度200mg/kg总Pb、2mg/kg总Cd复合污染土壤中施用有机磷肥,能有效钝化土壤DTPA-Pb、DTPA-Cd,但在400mg/kg总Pb、4mg/kg总Cd复合污染土壤中钝化效果有限,其优先钝化DTPA-Pb。施用发酵鸡粪不能有效钝化土壤DTPA-Pb、DTPA-Cd。(2)施用发酵鸡粪和有机磷肥均显著提高黑麦草鲜重。虽然施用有机磷肥能更有效的钝化土壤DTPA-Pb、DTPA-Cd,但对于黑麦草种植而言,施用发酵鸡粪能更有效的降低其对Pb和Cd的积累,并且主要积累到根部。(3)施用发酵鸡粪对土壤碱性磷酸酶活性、脱氢酶活性和脲酶活性有显著的促进作用。综合而言,湘西地区种植牧草黑麦草,施用发酵鸡粪比较合适,能有效改善土壤酸性,提高黑麦草鲜重和土壤酶活性,降低黑麦草对Pb和Cd的积累。     

基于总量及有效态的铜陵矿区农田土壤重金属生态风险评价

于铜陵矿区采集147个农田土壤样品,分析土壤样品中Cd、Cu、Pb、Zn 4种重金属总量和有效态含量,探讨该地区农田土壤重金属的污染现状、潜在生态风险和来源,并基于不同类型农田土壤有效态重金属的风险评价提出农作物种植建议。结果表明:铜陵矿区农田土壤重金属平均值普遍高于铜陵市土壤背景值,局部地区潜在生态风险极大;4种重金属元素的单项潜在生态危害指数依次为CdCuPbZn,铜陵矿区农田土壤重金属的潜在生态风险程度为中等,Cd为最主要的潜在生态危害因子;基于有效态重金属对不同类型农田土壤进行潜在生态风险评价,春季农田土壤的综合潜在生态危害指数排序为油菜地蔬菜地麦地,秋季农田土壤的综合潜在生态危害指数排序为稻田蔬菜地。基于上述结果,建议在重金属污染程度较高的区域实施小麦-蔬菜轮作,而在蔬菜种植中选择对重金属吸收能力较低的种类或品种。     

Evaluation of remediation process with plant-derived biosurfactant for recovery of heavy metals from contaminated soils

A washing process was studied to evaluate the efficiency of saponin on remediating heavy metal contaminated soils. Three different types of soils (Andosol: soil A, Cambisol: soil B, Regosol: soil C) were washed with saponin in batch experiments. Utilization of saponin was effective for removal of heavy metals from soils, attaining 90-100% of Cd and 85-98% of Zn extractions. The fractionations of heavy metals removed by saponin were identified using the sequential extraction. Saponin was effective in removing the exchangeable and carbonated fractions of heavy metals from soils. In recovery procedures, the pH of soil leachates was increased to about 10.7, leading to separate heavy metals as hydroxide precipitates and saponin solute. In addition recycle of used saponin is considered to be effective for the subsequent utilization. The limits of Japanese leaching test were met for all of the soil residues after saponin treatment. As a whole, this study shows that saponin can be used as a cleaning agent for remediation of heavy metal contaminated soils.     

Assessing heavy metal sources in agricultural soils of an European Mediterranean area by multivariate analysis

According to the European Thematic Strategy for Soil Protection, the characterization of the content and source of heavy metals in soils are necessary to establish quality standards on a regional level that allow the detection of sampling sites affected by pollution. In relation to this, the surface horizons of 54 agricultural soils under vegetable crops in the Alicante province (Spain), a representative area of the European Mediterranean region, were sampled to determine the content of Cd, Co, Cr, Cu, Fe, Mn, Ni, Pb and Zn. Analytical determinations were performed by atomic absorption spectroscopy after microwave sample digestion in acid solution. Results indicated that heavy metal levels were similar to those reported by authors working on agricultural soils from other parts of the Mediterranean region, with the exception of Cu and Pb in some samples. Multivariate analysis (principal component analysis and cluster analysis) was performed to identify a common source for heavy metals. Moreover, soil properties were determined in order to characterize agricultural soils and to analyze relationships between heavy metal contents and soil properties. The content of Co, Cr, Fe, Mn, Ni and Zn were associated with parent rocks and corresponded to the first principal component called the lithogenic component. A significant correlation was found between lithogenic metals and some soil properties such as soil organic matter, clay content, and carbonates, indicating an important interaction among them. On the other hand, elements such as Cd, Cu and Pb were related to anthropic activities and comprised the second (Cu and Pb) and third principal components (Cd), designated the anthropogenic components. Generally, Cd, Cu and Pb showed a lower correlation with soil properties due to the fact that they remain in available forms in these agricultural soils. Taking into account these results and other achieved in other parts of the European Mediterranean region, it can be concluded that soil quality standards are highly needed to declare soils affected by human induced pollution. This is particularly relevant for anthropogenic metals (Cd, Cu and Pb, and in some areas also Zn). Further research in other agricultural areas of the region would improve the basis for proposing such soil quality standards.     

Heavy metal contamination from mining sites in South Morocco: 1. Use of a biotest to assess metal toxicity of tailings and soils

Our work was conducted to investigate the heavy metal toxicity of tailings and soils collected from five metal mines located in the south of Morocco. We used the MetPAD biotest Kit which detects the toxicity specifically due to the heavy metals in environmental samples. This biotest initially developed to assess the toxicity of aquatic samples was adapted to the heterogeneous physico-chemical conditions of anthropogenic soils. Contrasted industrial soils were collected from four abandoned mines (A, B, C and E) and one mine (D) still active. The toxicity test was run concurrently with chemical analyses on the aqueous extracts of tailings materials and soils in order to assess the potential availability of heavy metals. Soil pH was variable, ranging from very acidic (pH 2.6) to alkaline values (pH 8.0-8.8). The tailings from polymetallic mines (B and D) contained very high concentrations of Zn (38,000-108,000 mg kg(-1)), Pb (20,412-30,100 mg kg(-1)), Cu (2,019-8,635 mg kg(-1)) and Cd (148-228 mg kg(-1)). Water-extractable metal concentrations (i.e., soil extracts) were much lower but were highly toxic as shown by the MetPAD test, except for soils from mines A, E and site C3 from mine C. The soil extracts from mine D were the most toxic amongst all the soils tested. On this site, the toxicity of soil water extracts was mainly due to high concentrations of Zn (785-1,753 mg l(-1)), Cu (1.8-82 mg l(-1)) and Cd (2.0-2.7 mg l(-1)). The general trend observed was an increase in metal toxicity measured by the biotest with increasing available metal contents in tailings materials and soils. Therefore, the MetPAD test can be used as a rapid and sensitive predictive tool to assess the heavy metal availability in soils highly contaminated by mining activities.     

Comparison of a rhizosphere-based method with other one-step extraction methods for assessing the bioavailability of soil metals to wheat

There is no method recognized as a universal approach for evaluation of bioavailability of heavy metals in soil. Based on the simulation of the rhizosphere soil conditions and integration of the combined effects of root-soil interactions as a whole, a rhizosphere-based method has been proposed. Wet fresh rhizosphere soil was extracted by low-molecular-weight organic acids (LMWOAs) to fractionate metal fractions of soil pools, which were then correlated with the metal contents of wheat roots and shoots. The rhizosphere-based method was compared with other one-step extraction methods using DTPA, EDTA, CaCl2, and NaNO3 as extractants and the first step of the Community Bureau of Reference (BCR) method. Simple correlation and stepwise multiple regression analysis were used for the comparison. Simple correlation indicated that the extractable Cu, Zn, Cr, and Cd of soils by the rhizosphere-based method were significantly correlated with the metal contents of wheat roots. For DTPA, BCR1 and EDTA methods there was a relatively poor correlation between the extractable Cu, Zn and Cd of soil and metal contents of wheat roots. Stepwise multiple regression analysis revealed that the equation of the rhizosphere-based method was the simplest one, and no soil properties variables needed to be added. In contrast, the equations of other one-step extraction methods were more complicated, and soil properties variables needed to be entered. The most distinct feature of the rhizosphere-based method was that the recommended method was suitable for acidic, neutral and near alkaline soils. However, the DTPA and EDTA extraction methods were suitable for calcareous soils only-or-only for acidic soils. The CaCl2, and NaNO3 extraction methods were only suitable for exchangeable metals. In short, the rhizosphere-based method was the most robust approach for evaluation of bioavailability of heavy metals in soils to wheat.     

In situ fixation of metals in soils using bauxite residue: chemical assessment

Contamination of soils with heavy metals and metalloids is a widespread problem all over the world. Low cost, non-invasive, in situ technologies are required for remediation processes. We investigated the efficiency of a bauxite residue (red mud) to fix heavy metals in two soils, one contaminated by industrial activities (French soil), and one by sewage sludge applications (UK soil). This Fe-oxide rich material was compared with lime, or beringite, a modified aluminosilicate that has been used for in situ fixation processes. Four different crop species were successively grown in pots. Metal concentrations in the soil pore waters were analyzed during the growing cycles. At the end of the experiment fluxes of heavy metals were measured using a diffusive gradient in thin film technique (DGT). Furthermore, a sequential extraction procedure (SEP) and an acidification test were performed to investigate the mechanisms of metal fixation by different soil amendments. In both soils, the concentrations of metals in the soil pore water and metal fluxes were greatly decreased by the amendments. An application of 2% red mud performed as well as beringite applied at 5%. Increasing soil pH was a common mechanism of action for all the amendments. However, the red mud amendment shifted metals from the exchangeable to the Fe-oxide fraction, and decreased acid extractability of metals. The results suggest that specific chemisorption, and possibly metal diffusion into oxide particles could also be the mechanisms responsible for the fixation of metals by red mud.     

Application of 16S rDNA-PCR amplification and DGGE fingerprinting for detection of shift in microbial community diversity in Cu-, Zn-, and Cd-contaminated paddy soils

Seven soils were sampled from farmland at different distances (0.01-5 km) from a copper and zinc smelter. The total contents of heavy metals in these soils ranged from 46 to 4895 mg Cu kg-1, 96 to 1133 mg Zn kg-1, and 6.9 to 28.8 mg Cd kg-1, respectively. The available fractions were highly correlated with total contents of the metals. In order to assess the impact of combined contamination of heavy metals on soil bacterial communities, denaturing gradient gel electrophoresis (DGGE) of polymerase chain reaction (PCR) amplicons of 16S rDNA sequence of bacteria in soil was used. Bacterial community structure was affected to some extent by heavy metals. The number of DGGE bands in soils increased with increasing distance from the copper and zinc smelter. Clustering analysis of the DGGE profiles showed that bacteria in the seven soils belonged to three clusters. Bacterial communities in three soils sampled at 0.01-0.60 km from the smelter belonged to one cluster, and those in three soils sampled at 0.8-1.2 km from the smelter belong to another cluster. Bacterial community in soil farthest from the smelter belonged to a single cluster. This study demonstrated that heavy metal contamination decreased both biomass and diversity of bacterial community in the soil.     

Retention and distribution of heavy metals in mangrove soils receiving wastewater

The distribution and chemical fractionation of heavy metals retained in mangrove soils receiving wastewater were examined by soil column leaching experiments. The columns, filled with mangrove soils collected from two swamps in Hong Kong and the People's Republic of China, were irrigated three times a week for 150 days with synthetic wastewater containing 4 mg l(-1) Cu, 20 mg l(-1) Zn, 20 mg l(-1) Mn and 0.4 mg l(-1) Cd. Soil columns leached with artificial seawater (without any heavy metals) were used as the control. At the end of the leaching experiments, soil samples from each column were divided into five layers according to its depth viz. 0-1, 1-3, 3-5, 5-10 and > 10 cm, and analyzed for total and extractable heavy metal content. The fractionation of heavy metals in the surface soil samples (0-1 cm) was investigated by the sequential extraction technique. In both types of mangrove soils, the surface layer (0-1 cm) of the columns receiving wastewater had significantly higher concentrations of total Cu, Cd, Mn and Zn than the control. Concentrations declined significantly with soil depth. The proportion of exchangeable heavy metals in soils receiving wastewater was significantly higher than that found in the control, about 30% of the total heavy metals accumulated in the soil masses of the treated columns were extracted by ammonium acetate at pH 4. The sequential extraction results show that in native mangrove soils (the soils without any treatment), the major portion of Cu, Zn, Mn and Cd was associated with the residual and precipitated fractions with very low concentrations in more labile phases. However, in mangrove soils receiving wastewater, a significantly higher percentage of Mn, Zn and Cd was found in the water-soluble and exchangeable fractions. Copper appeared to be more strongly adsorbed in mangrove soils than the other heavy metals. In general, heavy metal accumulation in the surface mangrove soils collected in Hong Kong was higher than those in the PRC, although the metals in the latter soil type were more strongly bound. These findings suggest that whether the heavy metal retained in managrove soils becomes a secondary source or a permanent sink would depend on the kinds of heavy metals and also the types of mangrove soils.     

某矿区土壤和地下水重金属污染调查与评价

为了解湘南某矿区土壤和地下水重金属污染状况,对该矿区东河流域附近重金属污染源进行了调查,同时,对地下水和土壤样品进行了采样分析,结果表明：（1）该矿区东河流域附近的主要污染源有18个,其中有色金属选厂、尾矿库、采矿场和冶炼厂是排放重金属较多的污染源;（2）20个采样点中土壤重金属Pb、Cd、Zn、As和Hg大部分超过国家土壤环境质量标准（GB15618-1995）,综合污染指数P综〉1,该矿区主要的重金属污染元素为Cd、As和Hg,且土壤中Cd、Zn和As的含量两两之间存在着极显著的正线性相关关系;（3）重金属元素在土壤中的纵向迁移不明显,该矿区附近20个采样点的地下水并未受到污染,综合污染指数P综〈1。20个采样点地下水Pb、Cd、Zn、As、Hg浓度均能达到地下水质量标准（GB／T14848．9）中的Ⅲ类标准。     

Degradability of ethylenediaminedisuccinic acid (EDDS) in metal contaminated soils: implications for its use soil remediation

Previous research has identified ethylenediaminedisuccinate (EDDS) as a promising biodegradable alternative for persistent compounds such as EDTA for application in soil washing or enhanced phytoextraction of heavy metals. This study examines heavy metal mobilization in three polluted soils varying in soil composition, with specific attention for competitive behaviour for complexation between the various metals and major elements, such as Al, Fe, Mn, Ca and Mg. In addition, amendment biodegradability was compared between the different soil types. The selected soils included a moderately contaminated calcareous clayey soil, a dredged sediment derived surface soil with similar soil characteristics yet more heavily polluted with Cd, Cr and Zn, and a sandy soil moderately contaminated by historical smelter activity (atmospheric deposition). Biodegradability of EDDS in the three soils varied distinctly. This was mainly expressed in the duration of the lag phase prior to metal complex degradation, and not so much in the half life when degradation effectively did set in. Differences in the lag phase were attributed to differences in soil pollution. However, EDDS was fully degraded within a period of 54 d in all soils regardless of initial delay. Assessment of the cation mobilisation patterns in the three soils under study revealed that mainly Ca, Fe and Al can reduce effectiveness of heavy metal mobilisation by competition for complexation.     

Genotypic and environmental variation in chromium, cadmium and lead concentrations in rice

Genotypic and environmental variation in Cr, Cd and Pb concentrations of rice grains and the interaction between these metals were investigated by using 138 rice genotypes grown in three contaminated soils. There were significant genotypic differences in the three heavy metal concentrations of rice grains, with the absolute difference among 138 genotypes in grain Cr, Cd and Pb concentrations being 24.5-, 9.1- and 23.8-folds, respectively, under the slightly contaminated soil (containing 4.61mgkg(-1) Cr, 1.09mgkg(-1) Cd and Pb 28.28mgkg(-1), respectively). A highly significant interaction occurred between genotype and environment (soil type) in the heavy metal concentrations of rice grains. Cr concentration in rice grains was not correlated with Cd and Pb concentration. However, there was a significant correlation between Cd and Pb in slightly and highly contaminated soils. The results suggest the possibility to develop the rice cultivars with low Cd and Pb concentrations in grain.