我国典型土壤对病毒等温静态吸附的数值模拟

通过室内等温静态批量平衡吸附实验,采用3种常见的等温线（Freundlich方程、Langmuir方程和Temkin方程）对2种病毒（MS2和X174）在2种处理（非灭菌和灭菌）条件下的6种土壤（红壤土、红粘土、乌栅土、黄泥土、沙质潮土和壤质潮土）中的吸附行为进行了回归拟合.实验结果和模拟结果均表明,土壤性质、病毒性质、土壤中的土著微生物对病毒在土壤中吸附行为均具有重要的影响.红粘土对MS2和X174的平均吸附比例几乎能达到100％,而2种潮土（沙质潮土和壤质潮土）相对较弱;总体来看土壤对X174的吸附能力高于MS2,但灭菌后的土壤对MS2的吸附能力却高于X174.在数值模拟中,Freundlich方程和Langmuir方程均具有理想的相关性.Freundlich方程能够表现出病毒浓度对其在土壤中吸附行为的影响;尽管Langmuir方程能够应用于土壤对病毒吸附能力的比较,但本研究中不能应用Langmuir方程来计算土壤对病毒的最大吸附量.     

荧光分光光度法测定土壤中石油类

建立了荧光分光光度法测定土壤中石油类.方法检出限为3 mg/kg,实际土壤加标回收率为95.5％ ～108％,精密度(RSD,n=6)为2.4％ ～8.7％.实验结果表明,该方法准确可靠、灵敏度高、选择性好、操作简便,与红外分光光度法有较好的可比性,满足土壤中石油类分析要求.     

铁、铝氧化物和土壤对苄嘧磺隆的吸附

用平衡吸附法研究了苄嘧磺隆在两种土壤(广州赤红壤、湖南红壤)和两种人工合成氧化物(针铁矿、铝氧化物)中的吸附,以及pH对吸附的影响.结果表明:(1)用Langmuir,Freundlich和Temkin等温方程描述供试样品对苄嘧磺隆的吸附,其中Freundlich吸附等温方程拟合的结果较佳.在苄嘧磺隆的实验浓度范围内和一定的pH条件下,吸附苄嘧磺隆的量随其浓度的升高而增加,其顺序为:铝氧化物＞湖南红壤＞针铁矿＞广州赤红壤.(2)苄嘧磺隆在供试样品中的吸附量随溶液pH值的升高而减小.     

贵州汞矿矿区不同位置土壤中总汞和甲基汞污染特征的研究

为了深入理解汞矿矿区土壤中总汞和甲基汞的污染特征,应用AAS、GC-CVAFS方法,分别对贵州万山、务川和滥木厂汞矿矿区不同位置土壤以及对照区土壤中的总汞(THg)和甲基汞(MeHg)进行了测定.结果表明,万山汞矿区土壤THg和MeHg含量范围分别为1.1～790 mg·kg^-1和0.19～15μg·kg^-1,务川汞矿区土壤THg和MeHg含量范围分别为0.33～317mg·kg^-1和0.41～20μg·kg^-1,滥木厂汞矿区土壤THg和MeHg含量范围分别为0.41～610 mg·kg^-1和0.70～8.8μg·kg^-1.对照区土壤汞含量明显低于矿区土壤,其THg和MeHg含量范围分别为0.14～1.2 mg·kg^-1和0.09～0.23μg·kg^-1;对照区土壤THg含量接近或稍高于全球背景土壤THg含量0.01～0.5 mg·kg^-1.研究表明,汞矿区稻田土壤具有较强的汞甲基化能力,其MeHg含量明显高于菜地和旱田土壤;万山汞矿区土壤汞污染程度明显高于滥木厂和务川汞矿区土壤汞污染.     

我国高速公路周边土壤重金属污染现状及研究进展

以我国高速公路周边土壤重金属为研究对象,综述了我国高速公路周边土壤重金属污染特征、影响因素、来源、环境风险及其研究进展。高速公路周边土壤主要受Pb、Cd、Cr、Cu、Zn等重金属污染,主要呈现指数分布、偏态分布和两者混合分布等特点,并且受到土地利用、风向、地形、车流量等多种因素的综合影响。土壤重金属的来源除了受成土母质等自然因素影响以外,公路交通和周边工农业活动也会对其来源产生较大影响。传统的土壤重金属评价方法主要采用单因子指数法、地累积指数法、生态风险评价法等对重金属的污染等级和环境风险进行评价。未来的研究应将重金属形态分析、空间和地统计分析、重金属稳定同位素示踪和源解析模型以及预测模型等多种手段相结合,开展高速公路周边土壤重金属的污染特征、时空分布、来源及预测预警研究等,为我国高速公路沿线工农业生产布局及其土壤重金属污染防控提供科学依据和决策支撑。     

New Metal Emission Patterns in Road Traffic Environments

The increased awareness of traffic as a major diffuse metal emission source emphasizes the need for more detailed information on the various traffic-related sources and how and where the metals are dispersed. In this study, metal emission patterns in the road traffic environment were examined from the perspective of different surrounding factors, e.g. the importance of intersections, deceleration, vehicle speed and traffic density. A total of 148 topsoil samples from 18 south Swedish roads were analysed (using GFAAS) for traffic-emitted metals, i.e. Cd, Cr, Cu, Ni, Pb, Sb and Zn. The roadside topsoil metal concentrations were used to examine correlations between metals and surrounding factors. The studied metals were divided into three groups corresponding to different emission sources: metals from decelerating activities (Cu, Sb and Zn), metals as historical residues from the combustion of petrol (Pb and Cd), and non-source-specific metals (Cr and Ni). It was found that Cu and Sb, despite their rather short history as traffic-emitted metals, have increased more than eightfold in roadside soils compared to background levels. The major source of road traffic related Cu and Sb is brake linings. The significant increase of Cu and Sb in roadside topsoil stresses the need for metal transport studies as well as effect studies of these metals. Metals emitted due to decelerating activities were not correlated to elevated concentrations near road junctions. Emission patterns of traffic-related metals alongside roads are crucial in order to be able to evaluate the optimal localization of storm water treatment ponds.     

Method optimization to measure polybrominated diphenyl ether (PBDE) concentrations in soils of Bratislava, Slovakia

We modified an analytical method to determine polybrominated diphenyl ethers (PBDEs) in urban soils of Bratislava (Slovakia). Gel permeation chromatography (GPC) introduced as a clean-up step for soil extracts substantially reduced matrix enhancements when PBDEs were measured with gas chromatography-negative chemical ionization-mass spectrometry (GC-NCI-MS). The resulting method proved to be accurate, precise, and showed low detection limits. The sum of 15 PBDE concentrations in surface horizons of Bratislava soils ranged from 87 to 627 pg g⁻¹. PBDE concentrations were mostly higher in surface than deeper horizons probably because of atmospheric deposition and lack of substantial vertical transport. Lower brominated PBDEs undergo more soil-atmosphere exchanges or are more scavenged and transferred with litter fall to the soil organic matter than higher brominated ones as suggested by the correlation between lower brominated PBDEs and soil organic C (C_org) concentrations.     

土壤重金属污染及其修复技术研究

土壤重金属污染物有汞、镉、铅、锌等,主要来源于交通运输、工业污染和农业污染。土壤重金属污染会导致农作物减产甚至死亡,对人体健康也会产生极大危害。目前土壤重金属污染修复的技术主要包括工程修复法、物理化学修复法、化学修复法和生物修复法。植物修复技术作为一种新兴的绿色、生态、高效的修复技术具有良好的发展前景。     

Inventory and vertical migration of 90Sr fallout and 137Cs/90Sr ratio in Spanish mainland soils

In this paper the inventory of ⁹⁰Sr in 34 points distributed along the Spanish peninsular territory is presented. Obtained values range between 173 Bq/m² and 2047 Bq/m². From these data set and those ¹³⁷Cs data obtained in a previous work the ¹³⁷Cs/⁹⁰Sr activity ratio has been established, laying this value between 0.9 and 3.6. Also the migration depth of both radionuclides has been analysed obtaining for ¹³⁷Cs an average value 57% lower than that obtained for ⁹⁰Sr.Additionally, this paper presents the results obtained in 11 sampling points in which the activity vertical profile has been measured. These profiles have been analysed to state the behaviour of strontium in soils and after, by using a convective-diffusive model, the parameters of the model which governs the vertical migration of ⁹⁰Sr in the soil, v (apparent convection velocity) and D (apparent diffusion coefficient) have been evaluated. Mean values obtained are 0.20 cm/year and 3.67 cm²/year, respectively.     

Remediation of metal-contaminated soils with the addition of materials--part I: characterization and viability studies for the selection of non-hazardous waste materials and silicates

Contamination episodes in soils require interventions to attenuate their impact. These actions are often based on the addition of materials to increase contaminant retention in the soil and to dilute the contaminant concentration. Here, non-hazardous wastes (such as sugar foam, fly ash and a material produced by the zeolitization of fly ash) and silicates (including bentonites) were tested and fully characterized in the laboratory to select suitable materials for remediating metal-contaminated soils. Data from X-ray fluorescence (XRF), N₂ adsorption/desorption isotherms, X-ray diffraction (XRD) and scanning electron microscopy/energy-dispersive X-ray spectroscopy (SEM-EDX) analyses revealed the chemical composition, specific surface area and the phases appearing in the materials. A pH titration test allowed the calculation of their acid neutralization capacity (ANC). The metal sorption and desorption capacities of the waste materials and silicates were also estimated. Sugar foam, fly ash and the zeolitic material were the best candidate materials. Sugar foam was selected because of its high ANC (17 000 meq kg⁻¹), and the others were selected because of their larger distribution coefficients and lower sorption reversibilities than those predicted in the contaminated soils.