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1.
Simultaneous competitive adsorption behavior of Cd, Cu, Pb and Zn onto nine soils with a wide physical–chemical characteristics from Eastern China was measured in batch experiments to assess the mobility and retention of these metals in soils. In the competitive adsorption system, adsorption isotherms for these metals on the soils exhibited significant differences in shape and in the amount adsorbed. As the applied concentration increased, Cu and Pb adsorption increased, while Cd and Zn adsorption decreased. Competition among heavy metals is very strong in acid soils with lower capacity to adsorb metal cations. Distribution coefficients (K dmedium) for each metal and soil were calculated. The highest K dmedium value was found for Pb and followed by Cu. However, low K dmedium values were shown for Zn and Cd. On the basis of the K dmedium values, the selectivity sequence of the metal adsorption is Pb > Cu > Zn > Cd and Pb > Cu > Cd > Zn. The adsorption sequence of nine soils was deduced from the joint distribution coefficients (K dΣmedium). This indicated that acid soils with low pH value had lower adsorption capacity for heavy metals, resulting in much higher risk of heavy metal pollution. The sum of adsorbed heavy metals on the soils could well described using the Langmuir equation. The maximum adsorption capacity (Q m) of soils ranged from 32.57 to 90.09 mmol kg−1. Highly significant positive correlations were found between the K dΣmedium and Q m of the metals and pH value and cation exchange capacity (CEC) of soil, suggesting that soil pH and CEC were key factors controlling the solubility and mobility of the metals in soils.  相似文献   

2.
《Applied Geochemistry》2003,18(11):1723-1731
The mobility and bioavailability of heavy metals depends on the metal retention capacity of soil and also on the geochemical phases with which metals are associated. Laboratory batch experiments were carried out to study the sorption and distribution of Cd, Ni and Pb in 3 soils differing in their physicochemical properties from India: Oxyaquic Haplustalf (SL1), Typic Haplustalf (SL2) and Typic Haplustert (SL3). The heavy metal adsorption was studied by isotherms and the distribution coefficient (KD) for each metal was obtained from the linear regressions of the concentration of metal remaining in equilibrium solution and the amount adsorbed. In general, the sorption capacity for all the metals decreased in the order: SL3>SL2>SL1. Among metals, the sorption capacity in all the soils decreased in the order: Pb>>Ni>Cd. Distribution of sorbed metals at various equilibrating concentrations was studied by sequential extraction. Results showed significant differences in the distribution of metals in these soils. At higher additions (such as 200 μM l−1) most of the metals were extracted in their more mobile fractions, exchangeable and/or inorganic in contrast to their original partitioning in soils, where they were preferentially associated with the less mobile residual fraction. Largest percentages of metals extracted in the exchangeable fraction corresponded to those soil–metal systems with smaller KD values, e.g. Cd, Ni and Pb in SL1 and Cd and Ni in SL2. In neutral and alkaline soils (SL2, pH=7.1, and SL3, pH=8.6) Pb was predominantly extracted from the inorganic fractions and this corresponded to higher KD values for Pb in these soils. The predominance of metals associated with the exchangeable fraction together with low KD values indicates higher mobility of metals retained in the acidic soil (SL1, pH=5.2) compared with the others.  相似文献   

3.
The competitive adsorption and the release of selected heavy metals and their speciation distribution before and after adsorption in the Yellow River sediments are discussed. The adsorption of metals onto sediments increases with increasing pH value and decreases with increasing ionic strength. The competitive coefficient K c and the distribution coefficient K d are obtained to analyze the competitive abilities of selected heavy metals, which are ranked as Pb > Cu >> Zn > Cd. The competition among selected heavy metals becomes more impetuous with increasing ion concentration in water. Speciation analysis was done by an improved analytical procedure involving five steps of sequential extraction. Cu, Pb and Zn were mainly transformed into the carbonate-bound form (50.8–87.7%) in adsorption. Most of (60.7–77.3%) Cd was transformed into the exchangeable form, and the percentage of carbonate-bound Cd was 19.7–30.4%. The release reaction was so quick that the release capacity of selected heavy metals from sediments to aqueous solution reached half of the maximum value only in 30 s. As opposed to adsorption, the release capacities of selected heavy metals were ranked as Cd > Zn >> Cu > Pb. In this study, Cd produces the most severe environmental hazards, because its concentration in the release solution is 85.8 times more than the human health criteria of US EPA.  相似文献   

4.
Calcareous vertisol soil is the dominant agricultural soil type and covers over 80% of the agricultural cultivated land in Jordan. This type of soil is characterized by its high pH and CaCO3 content, which made the heavy metals including Zn to be oxidized and adsorbed onto soil. Therefore, this type of soil is regarded as potentially Zn deficient. The effect of Zn initial concentration and average rainfall on the Zn adsorption and desorption from three types of calcareous vertisol soils has been examined. The amount of Zn adsorbed and desorbed at equilibrium increased with increasing Zn initial concentration for each of the three investigated soils. However, the percentage of adsorption and desorption decreased as the initial concentration of Zn ions increased. Moreover, results showed that rainfall has no influence on the behavior of Zn in the calcareous vertisol soils. Freundlich and Redlich-Peterson models provide the best representation of the experimental data, followed by the Langmuir model.  相似文献   

5.
Apparent overall equilibrium constants for the adsorption of Cd, Cu, Ni, Pb and Zn onto natural iron oxyhydroxides have been calculated from the partitioning of these trace metals in oxic lake sediments and the in situ measurement of trace metal concentrations in the associated pore waters. Such values obtained from lakes of various pH located on the Precambrian Shield, in the area of Sudbury, Ontario, are compared with equilibrium constants obtained for the adsorption of the trace metals onto iron oxyhydroxides in well-defined media.The field data are consistent with laboratory experiments reported in the literature and with theory. Both the influence of pH upon adsorption and the binding strength sequence observed for the field data agree with theory. At high sediment pH values, the partitioning of Cd, Ni and Zn between the pore waters and the natural iron oxyhydroxides is similar to those reported in the literature for the adsorption of these metals at low surface coverage onto amorphous iron oxyhydroxides in a NaNO3 medium; deviation from this simple model is however observed for Cu and Pb, presumably due to the competitive action of dissolved ligands. At low sediment pH values, the adsorption is much higher than predicted by the simple model and can be explained by the formation of ternary complexes with the iron oxyhydroxide surface.  相似文献   

6.
《Applied Geochemistry》1997,12(3):243-254
Column flow-through experiments reacting wastewater solutions with sandy loam soil samples were performed to study heavy metal attenuation by two soils with different physical and chemical properties. Reacted soil columns were leached with synthetic acid rain to study the mobility of attenuated heavy metals under leaching conditions. This study demonstrates that cation exchange, surface adsorption, chelation with solid organic material, and precipitation were the important attenuation mechanisms for the heavy metals (Cd, Cr, Cu, Mo, Ph, and Zn). Adsorption on soil hydrous oxide surfaces was the primary attenuation mechanism for Cd and Zn in both soils, and for Cu in a soil with low organic matter content. Wastewater solution pH is also an important factor that influences the retention of heavy metals. Cadmium, Cu, Cr, and Zn became mobile after prolonged application of spiked wastewater solution, either through saturation of soil adsorption sites or due to decreasing pH. Only Cr, Pb, and Mo, which are attenuated primarily through precipitation, show significant net retention by soil. Acid rain water removed heavy metals left in the column residual pore solution and weakly sorbed heavy metals in the soils, and has the ability to mobilize some strongly attenuated heavy metals, especially when the soil organic matter content is high. The results have important applications in predicting heavy metal mobility in contaminated soil, the disposal of acid mine drainage, and assessing the risks of landfall leachate leakage.  相似文献   

7.
在土壤中重金属含量较低的情况下,重金属的高光谱特征响应非常微弱,不易构建精确的高光谱直接反演模型。为了解决上述问题,依据土壤化学变量间的理化性质,将重金属富集特征转移到与之相关的化学主量元素上,使重金属微弱的信息得以间接定量反演。文中以海伦市黑土土壤为研究对象,通过主成分分析、聚类分析确定了主量元素氧化铁（Fe2O3）与微量重金属As、Zn、Cd之间存在明显吸附赋存关系。选用偏最小二乘法构建了研究区氧化铁含量的最佳反演模型（决定系数为0.704,均方根误差为0.148,F检验为12.732）,并利用氧化铁与As、Zn、Cd之间的赋存关系,通过神经网络构建了氧化铁预测值与重金属真实值间的非线性拟合模型,得出As含量的拟合程度最高,Zn的拟合程度较好,Cd的拟合效果较理想,总体相关性分别为0.796、0.732、0.530。研究结果表明,基于氧化铁含量的间接预测模型能对微量重金属As、Zn、Cd进行较好的定量预测,为微量重金属含量的定量分析提供了新的方法参考,为高光谱遥感技术预测土壤重金属含量提供了依据,增强了土壤微量重金属反演可行性,对细化自然资源质量监测、深化开展地学系统综合分析与评价有重要意义。   相似文献   

8.
Experimental data obtained on the adsorption–precipitation immobilization of heavy metals (Cu, Zn, Pb, Cd, Co, and Ni) from acidic and neutral solutions by calcite and dolomite demonstrate that interaction of solutions of heavy metals with these minerals at pH > 7.8–8.1 leads to a significant decrease in the concentrations of the metals because of the crystallization of carbonates of these metals. Except Pb, which is equally removed from solutions by both minerals, the immobilization efficiency of the metals on dolomite is greater than on calculate at the same pH. Residual Zn, Cd, Co, and Ni concentrations are immobilized by chemosorption, which is the most efficient for Cd and less significant for Co, Ni, and Zn. It is proved that artificial geochemical barriers on the basis of carbonate rocks can be efficiently applied to protect environment from contamination with heavy metals.  相似文献   

9.
浙北地区土壤元素有效量及其影响因素研究   总被引：7，自引：0，他引：7       下载免费PDF全文
浙江省北部地区调查研究表明,受成土母质来源、土壤类型及其理化性质等因素的影响,土壤元素全量、有效量及其有效度表现为:1)低山丘陵岗地土壤中As,Cd,Mo,Pb和Se全量较高,As,Cd,Fe,Pb,Se和Zn有效量较高;而山前平原区土壤中Hg,Pb和Zn元素全量较高,由地表向深部的下降递度较小,显示为原始沉积成因特点。2)中酸性、富含有机质的红壤和水稻土中As,Cd,Cu,Fe,Mn,Pb,Se,Zn等元素有效度较高,水稻土Hg有效度最低;弱碱性或碱性、贫有机质的潮土和滨海盐砂土中As,Cd,Cu,Fe,Mn,Pb,Se,Zn等元素有效量较低,但B有效量及有效度均较高。3)统计分析表明,土壤中Mn,Cu,Zn,Mo,Cd,Pb,Se等元素全量与有效量间具显著正相关性,表明全量是有效量的重要影响控制因素;有机质含量与Fe,Cu,Zn,Cd,As和Pb有效度间为显著正相关,说明有机质较高有利于土壤元素活化;Fe,Cu,Zn,Cd,As,Pb和Se有效度与pH值为显著负相关,表明土壤酸性增强(酸化)会增加这类元素的生物有效性。  相似文献   

10.
An exploratory study on soil contamination of heavy metals was carried out surrounding Huludao zinc smelter in Liaoning province, China. The distribution of total heavy metals and their chemical speciations were investigated. The correlations between heavy metal speciations and soil pH values in corresponding sites were also analyzed. In general, Cd, Zn, Pb, Cu and As presented a significant contamination in the area near the smelter, comparied with Environmental Quality Standards for Soils in China. The geoaccumulation index showed the degree of contamination: Cd > Zn > Pb > Cu > As. There was no obvious pollution of Cr and Ni in the studied area. The speciation analysis showed that the dominant fraction of Cd and Zn was the acid soluble fraction, and the second was the residual fraction. Pb was mostly associated with the residual fraction, which constituted more than 50% of total concentration in all samples. Cu in residual fraction accounted for a high percentage (40–80%) of total concentration, and the proportion of Cu in the oxidizable fraction is higher than that of other metals. The distribution pattern of Pb and Zn was obviously affected by soil pH. It seemed that Pb and Zn content in acid solution fraction increased with increasing soil pH values, while Cd content in acid soluble fraction accounted for more proportion in neutral and alkaline groups than acidic one. The fraction distribution patterns of Cu in three pH groups were very similar and independent of soil pH values. And the residual fraction of Cu took a predominant part (50%) of the total content.  相似文献   

11.
Chemical composition and equilibrium trends in mine pit lakes were examined to provide guidance for the application of geochemical models in predicting future lake water quality at prospective open pit mines. Composition trends show that elevated solute levels generally occur only at the extremes of acidic and alkaline pH conditions. Concentrations of cationic metals (Al, Cd, Cu, Fe, Mn, Pb, and Zn) are elevated only in acidic pit lakes, whereas anionic metalloids (As and Se) are generally elevated only in alkaline pit lakes. These trends are indicative of sulfide mineral oxidation and evapoconcentration for acidic and alkaline conditions, respectively.For nearly all pit lakes, SO4 is the dominant solute, but is limited by gypsum solubility. Fluorite, calcite, and barite are also important solubility controls. Well-defined solubility controls exist for the major metals (Al, Fe, Mn), including jurbanite and alunite for Al, ferrihydrite for Fe, and manganite, birnessite, and, possibly, rhodochrosite for Mn. Determinations of definite controls for the minor metals are less distinct, but may include otavite for Cd, brochantite and malachite for Cu, cerrusite and pyromorphite for Pb, and hydrozincite and Zn silicates for Zn. Concentrations of As and Se appear to be limited only by adsorption, but this control is sharply diminished by increased pH and SO4 concentration. In general, the concentrations of minor metals in pit lakes are not well represented by the theoretical solubilities of pure-phase minerals contained in the thermodynamic databases. Hence, modeling efforts will generally have to rely on empirical data on the leaching characteristics of pit wall-rocks to predict the concentrations of minor metals (Cd, Cu, Pb, Zn) in mine pit lakes.Methodologies for predicting pit lake water chemistry are still evolving. Geochemical and equilibrium trends in existing pit lakes can provide valuable information for guiding the development and application of predictive models. However, mineralogical studies of pit lake sediments, suspended particles, and alteration assemblages and studies of redox transformations are still needed to validate and refine the representations of geochemical processes in water quality models of mine pit lakes.  相似文献   

12.
Proton binding constants for the edge and basal surface sites of kaolinite were determined by batch titration experiments at 25 °C in the presence of 0.1 M, 0.01 M and 0.001 M solutions of NaNO3 and in the pH range 3-9. By optimizing the results of the titration experiments, the ratio of the edge sites to the basal surface sites was found to be 6:1. The adsorption of Cd(II), Cu(II), Ni(II), Zn(II) and Pb(II) onto kaolinite suspensions was investigated using batch adsorption experiments and results suggested that in the lower pH range the metallic cations were bound through non-specific ion exchange reactions on the permanently charged basal surface sites (X−). Adsorption on these sites was greatly affected by ionic strength. With increasing pH, the variable charged edge sites (SOH) became the major adsorption sites and inner-sphere specifically adsorbed monodentate complexes were believed to be formed. The effect of ionic strength on the extent of adsorption of the metals on the variable charged edge sites was much less than those on the permanently charged sites. Two binding constants, log K(X2Me) and log K(SOMe), were calculated by optimizing these constants in the computer program FITEQL. A model combining non-specific ion exchange reactions and inner-sphere specific surface complexations was developed to predict the adsorption of heavy metals onto kaolinite in the studied pH range. Linear free energy relationships were found between the edge site binding constants and the first hydrolysis constants of the metals.  相似文献   

13.
《Applied Geochemistry》2003,18(4):527-538
Thermodynamic parameters for proton and metal adsorption onto a gram-negative bacterium from the genus Enterobacteriaceae have been determined and compared with parameters for other strains of bacteria. Potentiometric titrations were used to determine the different types of sites present on bacterial cell walls. Stability constants for adsorption of Pb, Cu and Zn to specific sites were determined from batch adsorption experiments at varying pH with constant metal concentration. Titrations revealed 3 distinct acidic surface sites on the bacterial surface, with pK values of 4.3±0.2, 6.9±0.5 and 8.9±0.5, corresponding to carboxyl, phosphate and hydroxyl/amine groups, with surface densities of 5.0±0.7×10−4, 2.2±0.6×10−4 and 5.5±2.2×10−4 mol/g of dry bacteria. Only carboxyl and phosphate sites are involved in metal uptake, yielding the following intrinsic stability constants: Log Kcarboxyl: Zn=3.3±0.1, Pb=3.9±0.8, and Cu=4.4±0.2, Log Kphosphoryl: Zn=5.1±0.1 and Pb=5.0±0.9. The deprotonation constants are similar to those of other strains of bacteria, while site densities are also within an order of magnitude of other strains. The similarities in surface chemistry and metal stability constants suggest that bacteria may be represented by a simple generic thermodynamic model for the purposes of modelling metal transport in natural environments. Comparison with oxide-coated sand shows that bacteria can attenuate some metals to much lower pH values.  相似文献   

14.
洪涛  谢运球  赵一  杨利超 《中国岩溶》2016,35(4):439-445
为探讨硫铁矿冶炼区不同土地利用方式和土壤类型对重金属元素迁移的影响,采集了毕节市林口废弃硫铁矿冶炼厂内耕地砂壤土及附近林地石灰土表层和深层样共40组。室内测试土壤理化指标Pb、Zn、Cd全量和有效态含量,并对重金属元素含量的水平和垂直分布特征及重金属元素含量的相关性进行了讨论。结果表明:土壤中Pb和Zn的含量均符合土壤环境质量二级标准值,耕地表层土壤Cd含量是贵州省农业土壤背景值的7倍。土壤Cd有效态含量占全量的比值最大,而Pb和Zn有效态含量占全量的比值差别较小。耕地砂壤土Zn和Cd的全量随剖面深度的增加表现为先增大后减小,Pb呈减少的趋势;Pb和Zn的有效态含量随剖面深度的增加而减少,Cd有效态含量呈波动变化。林地石灰土中Pb、Zn、Cd的全量和有效态含量均随剖面深度的增加而减少,且Pb、Zn、Cd全量之间及全量与有效态含量之间都具有显著的正相关关系,而在耕地中各元素的相关性不明显。土壤频繁的扰动和偏酸性的环境有利于重金属垂向迁移。   相似文献   

15.
作物对土壤中重金属的吸收受作物种类、采集部位及土壤理化性质等多方面因素的影响。近年来,金衢盆地土壤酸化面积逐年增大,酸化程度逐渐加深,其对土壤-作物系统中重金属元素的活动影响尚不明确。本文基于金衢盆地典型地区264组根系土壤-稻米样品分析数据,开展土壤、作物的重金属含量特征及其影响因素的研究,重点讨论了土壤pH对作物吸收重金属的影响。结果表明：①264件土壤中多数重金属元素的变异系数大于0.5,As、Cd、Cr、Cu、Ni和Zn元素之间呈显著正相关（P<0.01）。土壤Cd超标样品23件,超标率为8.7%;As、Cr、Cu、Hg、Ni、Pb和Zn超标样品均未超过2件。②稻米中Cu、Zn与Cd含量呈显著正相关,Cd的富集系数（BCF）高于植物营养元素Cu、Zn。③稻米中Zn和Cu在P<0.1水平上与pH值呈显著正相关。Cd、Cr、Hg的BCF与pH值之间存在一定的负相关性。研究认为,适当调低土壤的酸碱度会削减土壤中Cd、Hg等重金属元素的活性,从而减少农作物对重金属的吸收转运。研究结果可为当地粮食安全生产决策提供科学数据,为土地管护提供参考依据。  相似文献   

16.
The charged sites on soil particles are important for the retention/adsorption of metals. Metallic counterions can neutralize the intrinsic charges on the surfaces of soil particles by forming complexes. In this study, efforts have been made to determine the effect of surface potential, pH, and ionic strength on the adsorption of four metal ions, hexavalent chromium Cr(VI), trivalent chromium Cr(III), nickel Ni(II) and cadmium Cd(II), in glacial till soil. Batch tests were performed to determine the effect of pH (2–12) and ionic strength (0.001–0.1 M KCl) on zeta potential of the glacial till soil. The point of zero charge (pH PZC ) of glacial till was found to be 7.0±2.5. Surface charge experiments revealed the high buffering capacity of the glacial till. Batch adsorption experiments were conducted at natural pH (8.2) using various concentrations of selected metals. The adsorption data was described by the Freundlich adsorption model. Overall glacial till shows lower adsorption affinity to Cr(VI) as compared to cationic metals, Cr(III), Ni(II) and Cd(II).  相似文献   

17.
Various soil zones such as Bw, C1, and C3 are developed on spilite. Montmorillonite, vermiculite and chlorite is moderately occurred in the C1 and C3 soil zones, in contrast montmorillonite and vermiculite are absent in Bw soils whereas illite and sesquioxide are relatively increased. The high cation exchange capacity (CEC) of montmorillonite and vermiculte and moderate CEC of chlorite and illite resulted in the high adsorption of heavy metals. The adsorption of the heavy metals on spilite soil zones was studied at different concentrations and pH levels. Heavy metals like lead, cadmium, and copper were selected for adsorption studies considering their contribution as toxic metals in the environment. The initial solute concentrations ranged from 7.0 × 10−3 to 1.0 × 102 mg/L. The sorption behavior of Cd2+, Pb2+, and Cu2+ on soil zones of spilite was investigated using the batch equilibrium technique at 25°C. The characteristics of the adsorption process were investigated using Scatchard plot analysis (q/C vs. q) by the batch equilibrium technique at 25°C. In the adsorption of heavy metals, deviation from linearity in the plot of q/C versus q was observed, indicating the presence of multi-model interaction and non-Langmuirean behavior. When the Scatchard plot showed a deviation from linearity, greater emphasis was placed on the analysis of the adsorption data in terms of the Freundlich model, in order to construct the adsorption isotherms of the metal(s) at particular concentration(s) in solutions. The adsorption behavior of these metal ions on spilite soil zones is expressed by the Freundlich isotherms. Adsorption constants and correlation coefficients for the Cd, Pb, and Cu on spilite soil zones were calculated from Freundlich plots.  相似文献   

18.
In water repellent soil, Cr, Pb and Cu showed higher adsorption intensities than Zn, Cd and Ni did. Soil water repellency is much more widespread than formerly thought. In order to promote fertility and productivity, the irrigation of recycled water onto water repellent soil may be an applied technology to be used in some areas of Southern Australia. Therefore, heavy metals in recycled water potentially enter into the soil. The competitive sorption and retention capacity of heavy metals in soil are important to be determined, especially considering the special geochemical origin of water repellent soil that was caused by waxes on or between the soil particles. Batch equilibrium sorption experiments on Cd, Cr, Cu, Ni, Pb and Zn in their typical proportion in recycled water were conducted in water repellent soil. The sorption intensity, sorption isotherm in the experiments together showed that Cr, Pb and Cu have higher sorption intensity than those of Zn, Ni and Cd in the competitive system. The risk assessment for the application of recycled water onto water repellent soil is definitely necessary, especially for the metal cations with relatively weak sorption.  相似文献   

19.
Vegetation at mining sites can produce increased heavy metal leaching by the organic acids and protons originating from root secretion and litter degradation. Batch experiments were conducted to investigate the effects of organic acids and pH on the extraction of Pb, Cd, Zn and Cu from an alkaline mine soil (sampled from a mining site of Chenzhou City, Hunan Province) and an acid mine soil (sampled from a mining site of Daxin county, Guangxi Province). The results showed that in the presence of organic acids (acetic, oxalic, malic, fumaric, tartaric and citric acids) at pH 7, the extraction of Pb, Cd, Zn and Cu from the acid mine soil was much higher than that from the alkaline mine soil, in which only citric acid with higher concentration was capable of extracting some heavy metals. Citric acid had the strongest ability in extracting heavy metals, followed by oxalic acid. Heavy metal extraction dramatically decreased with increasing pH. Moreover, at low pH, oxalic acid promoted the risk of Cu leaching; at high pH, the leaching of Pb, Zn, Cd and Cu was enhanced by both oxalic and citric acids. This indicated that those plants, which can produce substantial citric acid or oxalic acid by root secretion and litter degradation, should not be selected for the revegetation of mining sites.  相似文献   

20.
安永龙  黄勇  孙朝  邓凯文  李迪  黄丹 《地质通报》2018,37(6):1142-1149
为了监测北京市平原区2015年和2016年土壤中5种重金属As、Cd、Hg、Pb、Zn化学形态的变化趋势,运用Tessier连续提取法对土壤重金属进行了形态分析,并对影响重金属元素生物有效性的因素进行研究。结果表明,2年内研究区表层土壤重金属元素的形态变化微弱,有效态含量以Cd元素最高,达到45.67%,故潜在生态危害性最大;其次为Zn元素,达12.16%,其中碳酸盐结合态占比虽大,但由于研究区土壤呈偏碱性,Zn元素的迁移能力较弱,潜在危害性较小;As、Hg、Pb均以难迁移态存在,故潜在危害性也较小。土壤重金属元素的生物活性系数及迁移系数分别为:CdZnPbAsHg和CdAsZnPb=Hg,其中Cd元素2年的生物活性系数和迁移系数最高,展现出较强的生物活性和迁移能力,其余重金属元素的活性系数和迁移系数较低,潜在危害性较弱。影响重金属元素生物有效性的因素较复杂,以重金属元素全量为主,p H、有机质、CEC等理化性质次之。  相似文献   

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