复合淋洗剂对熔炼厂遗留场地土壤Pb、Cd的浸提效果

以某熔炼厂遗留场地重金属污染土壤作为研究对象,选取柠檬酸(CA)、复合聚天冬氨酸(PASP)、十二烷基苯磺酸钠(SDBS)作为淋洗剂,采用振荡淋洗法研究了不同浓度和配比的单一淋洗剂和复合淋洗剂对污染土壤Pb和Cd的去除效果。实验结果表明:CA、PASP、SDBS单独使用时对Pb和Cd的浸提率均随淋洗剂浓度提高而增大,CA对Pb、PASP对Pb、SDBS对Cd的最高浸提率分别为45.71%、63.69%和39.04%;CA-PASP复合淋洗剂淋洗Pb时有拮抗作用,单独使用PASP淋洗Pb效果更好,CA-PASP复合淋洗剂对Cd的浸提率较低;CASDBS复合淋洗剂效果最佳,对Pb和Cd的最高浸提率分别为55.22%和73.90%。     

柠檬酸淋洗去除电子垃圾污染土壤中的重金属

采用柠檬酸溶液对模拟电子垃圾污染土壤（简称污染土壤）中Cu,Pb,Cd 3种重金属进行淋洗实验,考察了柠檬酸溶液的浓度、柠檬酸溶液的pH、淋洗时间等对污染土壤中Cu,Pb,Cd的淋洗效果,探讨了柠檬酸溶液淋洗前后污染土壤中Cu,Pb,Cd 3种重金属各形态含量的变化。研究结果表明,在柠檬酸溶液的浓度0.100 mol/L、柠檬酸溶液的pH 5、淋洗时间1 440 min的适宜条件下,对污染土壤中Cu,Pb,Cd的去除率分别达到89.37%,72.11%,86.39%。柠檬酸溶液对3种重金属的去除主要是通过洗出酸可提取态（R1）和酸可还原态（R2）来实现的,每种重金属的R1和R2之和均占到其淋出总量的95%以上,而酸可氧化态（R3）和残渣态（R4）的含量淋洗前后基本无变化。     

复合重金属污染高岭土的电动修复

根据电子废弃物拆解场地的污染特征,以复合重金属(Cu,Cd,Pb)污染高岭土为研究对象,考察了电动技术对污染土壤的修复效果。实验结果表明:在电压梯度为1 V/cm、阳极液为自来水、阴极液为柠檬酸-柠檬酸钠缓冲液(pH=5)、靠近阴极设置活性炭渗透反应墙(PRB)的条件下电动修复96 h后,Cu,Cd,Pb的平均去除率分别可达79.93%,99.43%,39.36%;土壤的酸碱性对电动修复效果影响显著,通过在阴极添加缓冲液维持土壤偏酸性条件,有利于重金属污染物的电动去除;在靠近阴极设置活性炭PRB可富集重金属,减少阴极液的污染;迁移率大的酸可提取态重金属较易去除,残渣态重金属稳定性强,去除率较低。     

生物炭修复Cd,Pb污染土壤的研究进展

随着矿产开采、冶炼等工业活动以及污水灌溉、施用污泥和劣质化肥等农业活动的进行,Cd,Pb等有害重金属不断进入农业环境中,对农田、菜地等造成污染。生物炭作为重要的土壤改良剂,在对Cd,Pb污染土壤的修复中表现出巨大的潜力。从生物炭的特性及制备、修复效果及其影响因素、修复机理等方面,对近年来国内外有关生物炭修复Cd,Pb污染土壤的研究成果和现状进行了总结,并对生物炭修复Cd,Pb污染土壤的发展前景和未来研究方向进行了展望。     

脱硫用电石渣的重金属浸出特性及其对环境的影响

针对电厂用脱硫剂电石渣,分析了其基本组成及重金属浸出特性,为电厂脱硫设施的参数设计和环境影响评价提供依据和参考。研究结果表明,脱硫用电石渣主要成分为Ca（OH）2,含量在40%～50%之间;在8种重金属的含量中,只有Cd的含量超出土壤质量三级标准的要求,基本不会对土壤造成污染。浸出毒性试验表明,电石渣及其脱硫产物属于非危险废物,其各种重金属的浸出浓度主要受其本身重金属含量和最终pH的影响,这种影响在Pb、Cu和Cd上表现得较为突出,酸性环境下更有利于他们的浸出;碱性环境下有利于Pb和Ni的浸出。     

典型磷矿区表层土壤重金属空间分布特征研究

以开阳磷矿区为对象,结合地统计学普通克里金插值法以及单因素分析法,研究了矿区表层土壤重金属的空间分布特征,并对其进行了污染评价。结果表明：以矿区当地土壤重金属背景值为标准,Cu,Zn,Pb,Cd,As含量均存在超标情况;5种元素含量的变异程度均为高度变异,Pb,Cd,As的变异系数远大于Cu,Zn的变异系数;土壤重金属空间分布特征为Cd,As含量在东北部的积累程度大于西南部,东北—东南方向Cu,Zn,Pb,Cd,As的富集程度远大于西北—西南方向;不同土地利用类型对重金属的积累没有显著影响,这很可能与其他因素如背景值、风向、人类干扰（如化工产业）等有关。     

万山汞矿区土壤重金属污染特征及来源解析

以万山汞矿区土壤为研究对象,采用电感耦合等离子体质谱仪和原子荧光光谱仪测定土壤中的重金属含量,分别运用内梅罗综合污染指数（NPI）法和潜在生态风险指数（RI）法评价土壤重金属污染和潜在生态风险,并应用相关性分析、主成分分析和聚类分析对土壤重金属来源进行分析。结果表明：土壤Hg、Cd、As、Pb、Cu、Ni和Zn出现不同程度累积,分别达贵州省背景值的263.61、2.31、1.28、2.11、1.70、1.01和3.52倍;土壤重金属平均NPI为188.00,属于严重污染水平,Hg是主要污染因子;土壤重金属平均RI为10 655.70,属于极强潜在生态风险水平,Hg是主要潜在生态风险因子;土壤中Cu、Ni、Cr主要源于自然活动,As、Pb、Zn主要源于燃煤和交通运输污染,Cd主要源于农业污染,Hg主要源于汞冶炼污染。     

无患子皂苷与柠檬酸协同洗脱污染土壤中镉铅

以某废弃铅锌矿区重金属污染土壤为研究对象,采用无患子皂苷与柠檬酸(CA)协同洗脱污染土壤中的Cd和Pb.以无患子果皮投加量为20 g/L所得水浸提液和浓度为0.3 mol/L的CA配制复配淋洗剂.在浸提液中添加CA后,能有效提高对土壤中Pb的去除率.在浸提液和CA的体积比为1:3、淋洗剂pH为5、淋洗时间为12.0 h...     

喀斯特山区燃煤电厂土壤重金属污染评价

选取地处贵州省喀斯特山区的金沙电厂为研究对象,对电厂周围的表层土壤、蔬菜(莲花白)试样的重金属含量进行了测定,采用模糊数学法对土壤重金属污染进行了评价,采用富集系数法分析了莲花白对重金属的富集能力。实验结果表明:电厂周围表层土壤中Hg,As,Cd,Pb,Cu的平均含量分别达0.70,26.40,0.61,44.83,35.51 mg/kg,其中,Hg和Cd的平均含量分别为GB 15618—1995《土壤环境质量标准》中二级标准的1.40和2.03倍;电厂周围土壤受到较为严重的Hg,As,Cd污染,各个方向的重金属污染程度大小顺序为西北西东南西南东北东,总体趋势为西向大于东向;莲花白对土壤中Cd的富集作用较强,对其他重金属的富集作用较弱。     

土壤重金属污染治理存在的问题及应对措施

随着当前社会各界逐渐提高环保相关意识,土壤重金属污染问题受关注程度越来越高。土壤污染除了会影响整个土壤圈层之外,还会对诸如空气、水体等产生一定程度的污染。土壤重金属污染所涉及的重金属元素主要为Hg,Cd,Pb,Cr,As,Zn,Cu,Ni等。当前治理土壤重金属污染,不仅能够有效提高农产品安全,还能够保证人类的健康发展。分析土壤重金属污染的成因及其对农作物和人类所产生的影响,并尝试从物理、化学、生物等多个角度共同开展修复工作,以求可以为我国受污染土壤开展治理工作提供经验借鉴。     

Solubility and Potential Mobility of Heavy Metals in Two Contaminated Urban Soils from Stockholm,Sweden

The solubility and potential mobility of heavy metals (Cd, Cu,Hg, Pb and Zn) in two urban soils were studied by sequential andleaching extractions (rainwater). Compared to rural (arable) soils on similar parent material, the urban soils were highlycontaminated with Hg and Pb and to a lesser extent also with Cd,Cu and Zn. Metal concentrations in rainwater leachates were related to sequential extractions and metal levels reported fromStockholm groundwater. Cadmium and Zn in the soils were mainly recovered in easily extractable fractions, whereas Cu and Pb were complex bound. Concentrations of Pb in the residual fractionwere between two- and eightfold those in arable soils, indicatingthat the sequential extraction scheme did not reflect the solidphases affected by anthropogenic inputs. Cadmium and Zn conc. inthe rainwater leachates were within the range detected in Stockholm groundwater, while Cu and Pb conc. were higher, whichsuggests that Cu and Pb released from the surface soil were immobilised in deeper soil layers. In a soil highly contaminatedwith Hg, the Hg conc. in the leachate was above the median concentration, but still 50 times lower than the max concentration found in groundwater, indicating the possibilityof other sources. In conclusion, it proved difficult to quantitatively predict the mobility of metals in soils by sequential extractions.     

Heavy metal speciation in various types of fly ash from municipal solid waste incinerator

Fly ash (FA) from municipal solid waste incinerators has been known as hazardous waste, which is mostly because of the high content of heavy metal and dioxins. Besides the content, the form of the heavy metals in fly ash is also very important, because it is tightly related with the leaching behavior of fly ash in diverse circumstances. To evaluate the environment potential risk of fly ash, the Tessier chemical extraction method was adopted. In this study, four kinds of fly ash were examined, one sample from China (CFA) and the other three from Japan (RFA, CaFA and NaFA). Five metal elements were detected and they were Ni, Cr, Cd, Pb, and Cu. The result of total heavy metals’ concentration showed CFA has the lowest content. As to the Tessier chemical extraction experiments, the results show that Cd, Pb, and Cu have higher leaching risk in the environment than other heavy metals. The result of leaching test experiment showed that the more exchangeable speciation of Cd, Cr and Pb in FA, the more it could leach out in natural environment.     

Electrochemical remediation of heavy metal contaminated soils

Over the years, many soils have been contaminated with toxic heavy metals as a result of a variety of industrial and military activities. Electrokinetic soil treatment is an emerging technology that could prove to be very effective in the remediation of these sites. “Real-world” heavy metal contaminated (Pb(II), Cd(II), and Cr(III)) soils from three military sites with varying soil properties were subjected to electrokinetic treatment in the laboratory. Metal extractants (chelating agents and acids) were studied and found to be effective in enhancing the electrokinetic process. Results indicated that heavy metal removal efficiencies varied in the three soils tested. In one case, removal efficiencies of 90 percent and 60 percent were obtained for Cd and Cr, respectively, for the nitric acid amended experiments. For another case, over 60 percent of the total Pb in the system was deposited near the cathode for the non-amended and the citric-acid amended tests. Conversely, in the third case, the electrokinetic soil-washing treatment process failed to produce significant removal of any metal contaminant. The discrepancies that exist between the metal removal results of the three soils were attributed to the different physiochemical characteristics of each soil.     

Effects of Acid Rain on Competitive Releases of Cd, Cu, and Zn from Two Natural Soils and Two Contaminated Soils in Hunan, China

Leaching experiments of rebuilt soil columns with two simulated acid rain solutions (pH 4.6–3.8) were conducted for two natural soils and two artificial contaminated soils from Hunan, south-central China, to study effects of acid rain on competitive releases of soil Cd, Cu, and Zn. Distilled water was used in comparison. The results showed that the total releases were Zn>Cu>Cd for the natural soils and Cd>Zn≫Cu for the contaminated soils, which reflected sensitivity of these metals to acid rain. Leached with different acid rain, about 26–76% of external Cd and 11–68% external Zn were released, but more than 99% of external Cu was adsorbed by the soils, and therefore Cu had a different sorption and desorption pattern from Cd and Zn. Metal releases were obviously correlated with releases of TOC in the leachates, which could be described as an exponential equation. Compared with the natural soils, acid rain not only led to changes in total metal contents, but also in metal fraction distributions in the contaminated soils. More acidified soils had a lower sorption capacity to metals, mostly related to soil properties such as pH, organic matter, soil particles, adsorbed SO₄ ²⁻, exchangeable Al³⁺ and H⁺, and contents of Fe₂O₃ and Al₂O₃.     

硫酸锰渣污染土壤中重金属的形态分布及生物活性

测定了硫酸锰渣污染土壤中Cu,Zn,Cd,Pb,Mn的总量和各形态含量.结果表明重金属总量远超过环境背景值和土壤环境二级标准.重金属各形态分布特征:Cu,有机态>残渣态>铁锰氧化态>碳酸盐态>可交换态;Zn,残渣态>铁锰氧化态>有机态>碳酸盐态>可交换态;Cd,铁锰氧化态>可交换态>碳酸盐态>残渣态>有机态;Pb,铁锰氧化态>残渣态>有机态>碳酸盐态>可交换态;Mn,铁锰氧化态>残渣态>可交换态>有机态>碳酸盐态.重金属的生物可利用性系数和迁移系数均为Cd>Mn>Pb>Cu>Zn.