铅冶炼区土壤重金属总量和有效态含量的函数分析

采集铅冶炼企业周边3 000 m范围内220个表层土壤样品,测定了有毒有害元素铅、镉、砷和汞的总量和有效态含量,探讨了它们之间的关系。结果表明:研究区土壤受到汞、砷、铅、镉的污染依次明显严重,土壤重金属的总量和有效态含量的变异系数均大于100%,土壤镉、铅、汞、砷的生物有效性系数平均值分别为25.9%、17.2%、0.58%、0.11%。土壤铅、镉和砷的总量与其有效态含量呈显著正相关(P0.001),而汞的总量与其有效态含量的相关性不显著(P0.05)。土壤铅和镉的总量和有效态含量可以用直线函数和幂函数表达,函数反推的有效态值和对应统计值的变异系数不大于10%。     

火焰原子吸收法测定大气降尘中的铜,铅,锌,镉

火焰原子吸收法测定大气降尘中的铜、铅、锌、镉康新立（山西省运城地区环保局０４４０００）杨俊玲（山西省运城地区药检所０４４０００）大气中重金属的测定，以往是将大气中重金属采集到氯乙烯滤膜上，用氯仿溶解滤膜后，直接用火焰原子吸收法进行测定，由于含量较低，...     

乌鲁木齐市"菜篮子"基地土壤环境质量现状调查

通过对乌鲁木齐市“菜篮子”种植基地——安宁渠土壤中重金属、农药、多环芳烃等污染物的监测结果分析得出,该区域内的土壤中总砷、总汞、总铬、总镉等重金属和土壤中六六六、滴滴涕等含量均低于国家标准限值,土壤污染综合指数属于安全级别之内,但与历史背景值相比,部分重金属含量呈现明显的增加趋势,尤其是总铅、总砷和总镉的含量增幅较大。污染增加趋势与城市工业发展和交通污染及施用化肥、农药有关。     

重庆某工业园土壤重金属污染特征、风险及源解析

以重庆市某工业园区表层土壤为研究对象,探讨了土壤重金属在不同季节的污染特征,利用污染指数法、健康风险模型和主成分/绝对主成分得分受体模型进行风险评价和源分析。结果表明:不同季节土壤样品间各重金属含量差异显著。35.5%的样品中汞含量超出土壤污染风险筛选值,其他元素未超标。与土壤背景值相比,各元素表现出不同程度的富集,汞超标约110~1300倍。内梅罗指数显示土壤整体和汞元素处于轻度污染及以下,其他元素为安全。潜在生态危害指数显示,土壤整体和汞属于极强污染,镉属于轻微~强污染,其他元素为轻微污染。土壤重金属总致癌风险为2.6×10^-7~1.0×10^-5,总非致癌风险熵均小于1,砷存在致癌风险,主要通过经口摄入暴露。秋季中,汞、六价铬、铅、镍、砷和铜来自工业源,镉主要来源于自然成因。春季中,镉和铅来自交通、冶金和燃煤等排放,镍、砷和铜源于冶炼和金属表面处理等排放,汞主要来自化工生产和燃料燃烧。交通运输、工业生产和燃料燃烧等污染的排放是土壤重金属的主要来源,今后应加强园区内汞、砷和镉的源头减排和治理。     

石墨炉原子吸收光谱法测定大气降水中镉镍铅

采用石墨炉原子吸收光谱法测定大气降水中镉、镍、铅，优化了试验条件。镉在0ug／L-5．00ug／L范围、镍和铅在0ug／L-20．0ug／L范围内线性良好，镉、镍、铅的检出限分别为0．03ug／L、0．79ug／L、1．37ug／L，大气降水样品测定的RSD为0．8％-2．6％，加标回收率为96．0％-106％。     

汽车废气中的铅对城市土壤污染状况调查

通过现场调查，定量分析了乌鲁木齐市市区交通主干道二侧土壤中铅、镉等6种元素的含量，初步掌握了重金属元素的分布情况。调查结果表明，在交通密集易形成堵车的路段，土壤中重金属富集的量较高，在交通顺畅或车流量少的路段，土壤中重金属含量相对较低。铅污染的主要来源是汽车尾气。     

广东某铅锌矿周边地区大气颗粒物重金属水平及人群暴露风险评价

以广东某典型铅锌矿周边地区为研究区域，通过实地监测空气中颗粒物重金属浓度水平，并结合暴露量计算，进行健康风险评价。结果表明：研究区大气TSP浓度满足所属功能区环境空气质量标准要求，但PM10浓度在个别监测点出现有单次超标现象，铅平均浓度符合年平均参照标准要求，镉平均浓度则超年平均参照标准要求；颗粒物重金属分析表明，该区域气象扩散条件较好，对照点中重金属含量与其他监控监测点的含量相当；靠近冶炼厂或铅锌矿的降尘重金属总量比远离的高，所以冶炼厂和铅锌矿对环境大气中重金属含量还是有一定的影响。大气颗粒物重金属暴露人群风险评价结果表明，研究区域不存在非致癌健康风险，但个别监测点则存在镉致癌风险警戒级别。     

大气降尘中铅、锌、铜、铁的原子吸收光谱法测定

研究了大气降尘中铅、锌、铜、铁等金属元素的原子吸收光谱测定方法,用氢氟酸消解法对降尘进行预处理,并对方法的精密度、准确度进行了检验,结果较为满意.该法简便、快速、灵敏.     

蔬菜与土壤环境中铅镉含量相关性调查

通过调查5种蔬菜对铅、镉绝对吸收量以及富集系数不同,分析了蔬菜与土壤中重金属含量相关性.结果表明,各种蔬菜对镉的吸收绝对量差异明显,同类型蔬菜对铅、镉的吸收量接近.各种蔬菜对铅的富集能力排序为白菜>黄瓜>番茄>青菜>辣椒,对镉的富集能力排序为青菜>白菜>辣椒>番茄>黄瓜.蔬菜对土壤中镉的吸收能力明显大于铅.     

电子废弃物拆解园区重金属排放特征和周边土壤重金属污染来源解析及风险评价

对某典型电子废弃物拆解园区排放的废气以及周边土壤中的重金属进行监测分析。结果显示，拆解过程中排放的重金属总量由高到低依次为：锡（Sn）、铬（Cr）、镍（Ni）、铅（Pb）、铜（Cu）、锑（Sb）、锰（Mn）、砷（As）、镉（Cd）、汞（Hg）；从处理工艺来看，几个主要拆解工序均有重金属排放，排放量由高到低依次为：加热烤板、火法冶炼、塑料造粒和湿法冶炼工序。园区周边土壤中的Hg、Cd、Cu、Pb平均质量分数超过珠三角土壤污染风险筛选值。相关性和主成分分析结果表明，Pb、Cu、Cd、Ni、Zn等重金属来源于电子废弃物拆解过程，包括废水排放、大气干湿沉降和固体废弃物随意堆放等途径，Cr可能主要来源于成土母质，Hg有电子废弃物之外的其他来源。土壤生态风险评价结果表明，该区域属于很强生态风险，其中Cd和Hg对生态危害的贡献率达到91.6%。土壤环境容量评价结果表明，该区域仅有As和Cr的土壤现存容量较大，Zn和Ni的土壤现存环境容量较小，已达到警戒值，其余重金属均处于超载状态。该地区土壤重金属污染状况须引起足够重视，应尽快制定管控治理措施。     

典型金属冶炼城市降尘中重金属污染特征及风险评价

2021年1-3月,采集湖南省某典型金属冶炼城市不同功能区的降尘样品,分析测定了17种重金属元素含量,其中15种重金属元素含量超出了湖南背景值,分别为Ag、Fe、Cd、Ti、Sb、Tl、Pb、As、Zn、Cu、Mo、Ni、Cr、Ba、Mn。采用地累积指数法、潜在生态危害指数法和健康风险评价模型对大气降尘中重金属可能造成的生态风险和健康风险进行评价。结果表明:受长期的有色金属冶炼影响,Ag、Cd、Fe、Sb、Ti、Tl 6种重金属达到了极重度污染,Pb、As、Zn、Cu、Mo在中度污染程度以上。工业区的综合生态危害指数远高于工业居民混合区、工业农业混合区、居民区和交通区,达到了极强生态危害级别。健康风险评价结果显示:大气降尘中As和Pb存在非致癌风险,As、Cd和Ni存在致癌风险,且经口摄入是最主要的暴露途径。与青少年和儿童相比,大气降尘中重金属对成人造成的风险较高,且成年女性面临的风险高于成年男性。     

燃煤电厂周边大气重金属污染特征及来源解析

为探究燃煤电厂周边大气环境中重金属的污染特征与来源,对广东某山区燃煤电厂周边地区环境和污染源的重金属进行测定,分析其污染特征,采用因子分析法和Pb同位素示踪法对环境中的重金属进行来源解析。结果表明,研究区域室内积尘中重金属浓度水平明显高于土壤重金属,污染空间分布与当地气象条件相关。环境空气TSP中重金属主要来自2个污染源,Cd、Pb、As主要来自电厂燃煤,Ca、Mn、Al、Mg主要来自土壤扬尘。TSP、降尘、积尘样品所含的Pb均与电厂采集的煤、炉渣、粉煤灰样品所含的Pb具有同源性,与其他污染源同源性不明显,说明研究区域大气中Pb污染主要来自电厂燃烧所排放的烟尘,其他污染源影响不大。     

Microscopic and chemical studies of metal particulates in tree bark and attic dust: evidence for historical atmospheric smelter emissions, Humberside, UK

Tree barks and attic dusts were examined as historical archives of smelter emissions, with the aim of elucidating the pathways of pollution associated with a plume of Sn and Pb contamination in top soils, found close to the former Capper Pass smelter, Humberside, UK. Samples were collected from three villages within the area of the contamination plume. Scanning electron microscopy (SEM) and bulk chemical analyses were used to assess particle type, number and deposition patterns. SEM analysis of dusts and bark revealed that Sn and Pb particles were present in samples from all three villages along with copper, zinc and iron particles. These were almost entirely <10 microm in diameter and occurred mostly as oxides, frequently forming clusters of sub-micron crystals. Samples further from the smelter contained considerably fewer particles. We present images of smelter derived Sn particles. Chemical assays of the barks and attic dusts demonstrated that concentrations of Sn, Pb, Cu, As, Sb and Cd diminished with increasing distance from the source. Strong positive correlations were found between Sn and Pb, As, Sb and Cd in the attic dusts. Enrichment factors (EF) were calculated for these trace elements based on topsoil element concentrations obtained from the soil survey of the study area. Decreases in these trace element concentrations and EF values with distance away from the smelter are consistent with trends found in the soil survey for Sn and Pb and are typical of deposition patterns around smelter stacks. The study demonstrates that tree bark and attic dusts can be effective archives of metal particulates deposited from large static emission sources.     

Determination of Pb and Cd in road dusts over the period in which Pb was removed from petrol in the UK

It is commonly agreed that automobile exhaust has been the most important source of Pb pollution in urban areas, and that Cd may come from wear and tear of tyres. This study evaluates the fall in Pb concentrations in road dusts in Manchester as a consequence of the removal of Pb from petrol in January 2000. In the work presented here a slurry graphite furnace atomic absorption methodology for the determination of Pb and Cd in road dusts has been developed and is compared with an acid digestion method in terms of efficiency. The reproducibility and accuracy of the results obtained by acid digestion and the slurry method have been studied and a certified reference material CRM 038 was analysed to confirm the reliability of the proposed methods. Different factors were evaluated throughout this work including: (i) the effect of traffic density on Pb and Cd levels in road dust samples collected weekly during the period of May 1999 until September 2000; (ii) comparison between the Pb and Cd levels in a busy road and a residential street; (iii) the effect of distance from the source on Pb and Cd levels; The results of these experiments show a reduction in Pb levels over the sampling period. The relationship between road dust particle size and Pb and Cd concentration was also investigated in the 4-250 microns size range using the slurry method, showing that there is a relationship between metal concentration and particle size; the highest concentrations being for the smallest particle size.     

Geochemical position of Pb,Zn and Cd in soils near the Olkusz mine/smelter,South Poland: effects of land use,type of contamination and distance from pollution source

The soils adjacent to an area of historical mining, ore processing and smelting activities reflects the historical background and a mixing of recent contamination sources. The main anthropogenic sources of metals can be connected with historical and recent mine wastes, direct atmospheric deposition from mining and smelting processes and dust particles originating from open tailings ponds. Contaminated agriculture and forest soil samples with mining and smelting related pollutants were collected at different distances from the source of emission in the Pb–Zn–Ag mining area near Olkusz, Upper Silesia to (a) compare the chemical speciation of metals in agriculture and forest soils situated at the same distance from the point source of pollution (paired sampling design), (b) to evaluate the relationship between the distance from the polluter and the retention of the metals in the soil, (c) to describe mineralogy transformation of anthropogenic soil particles in the soils, and (d) to assess the effect of deposited fly ash vs. dumped mining/smelting waste on the mobility and bioavailability of metals in the soil. Forest soils are much more affected with smelting processes than agriculture soils. However, agriculture soils suffer from the downward metal migration more than the forest soils. The maximum concentrations of Pb, Zn, and Cd were detected in a forest soil profile near the smelter and reached about 25 g kg^− 1, 20 g kg^− 1 and 200 mg kg^− 1 for Pb, Zn and Cd, respectively. The metal pollutants from smelting processes are less stable under slightly alkaline soil pH then acidic due to the metal carbonates precipitation. Metal mobility ranges in the studied forest soils are as follows: Pb > Zn ≈ Cd for relatively circum-neutral soil pH (near the smelter), Cd > Zn > Pb for acidic soils (further from the smelter). Under relatively comparable pH conditions, the main soil properties influencing metal migration are total organic carbon and cation exchange capacity. The mobilization of Pb, Zn and Cd in soils depends on the persistence of the metal-containing particles in the atmosphere; the longer the time, the more abundant the stable forms. The dumped mining/smelting waste is less risk of easily mobilizable metal forms, however, downward metal migration especially due to the periodical leaching of the waste was observed.     

再生铅企业土壤-地下水中重金属污染迁移特征

为了解某再生铅企业厂区土壤和浅层地下水重金属污染状况,采集了96个土壤样品和4个地下水样品,定量分析了其Pb,Cd,As的含量及空间分布特征,探讨企业生产对环境造成的影响。结果表明,该区域土壤中Cd、As、Pb超标率分别为67.0%,35.1%,11.7%,在厂区呈现局部富集现象,最大值是土壤背景值的几十倍乃至数千倍;在垂直方向上由于Pb,Cd,As在土壤中迁移率较低,其值随深度增加呈总体下降趋势;该区域地下水中Pb,Cd,As值远低于地下水质量标准值。     

典型涉污企业周边土壤重金属污染特征及潜在生态风险评价

分析和评价典型涉污企业周边土壤环境质量,对于加强企业用地环境风险管控,实施土壤重金属污染精准防控,进一步保障农产品质量安全具有重要意义。以18类典型涉污企业周边土壤为研究对象,对475家企业周边的2 017个监测样点进行土壤重金属Cd、As、Pb、Hg、Cr、Cu、Zn和Ni元素含量测定,并采用主成分分析法、Hakanson 潜在生态风险指数法进行分析及评价。结果表明:典型涉污企业周边土壤重金属污染以Cd、Pb和As元素为主,各元素含量超过土壤污染风险筛选值的样品比例为9.82%~31.0%,超过土壤污染风险管控值的样品比例为4.46%~13.1%,其次是Zn、Cu、Hg和Ni,Cr无明显污染;主要污染元素Cd、Pb、As、Zn和Cu来自相同污染源且主要分布在有色金属矿采选业(B9)、黑色金属冶炼和压延加工业(C31)、有色金属冶炼和压延加工业(C32)、生态保护和环境治理业(N77)等行业企业周边;黑色金属冶炼和压延加工业(C31)、有色金属矿采选业(B9)、有色金属冶炼和压延加工业(C32)等行业企业周边土壤重金属潜在生态风险等级较高,中等风险及以上比例分别为76.0%、53.0%和54.1%。可见,典型涉污企业周边土壤重金属存在一定程度的污染,尤其是有色金属矿采选业(B9)等采矿业以及黑色金属冶炼和压延加工(C31)等制造业等,污染程度高,潜在生态风险大,需要加强监测和管控。     

Characterization and Identification of the Sources of Chromium, Zinc, Lead, Cadmium, Nickel, Manganese and Iron in Pm10 Particulates at the Two Sites of Kolkata, India

Monitoring of ambient PM₁₀ (particulate matter which passes through a size selective impactor inlet with a 50% efficiency cut-off at 10 μm aerodynamic diameter) has been done at residential (Kasba) and industrial (Cossipore) sites of an urban region of Kolkata during November 2003 to November 2004. These sites were selected depending on the dominant anthropogenic activities. Metal constituents of atmospheric PM₁₀ deposited on glass fibre filter paper were estimated using Inductively Coupled Plasma Atomic Emission Spectrometer (ICP-AES). Chromium (Cr), zinc (Zn), lead (Pb), cadmium (Cd), nickel (Ni), manganese (Mn) and iron (Fe) are the seven toxic trace metals quantified from the measured PM₁₀ concentrations. The 24 h average concentrations of Cr, Zn, Pb, Cd, Ni, Mn and Fe from ninety PM₁₀ particulate samples of Kolkata were found to be 6.9, 506.1, 79.1, 3.3, 7.4, 2.4 and 103.6 ng/m³, respectively. The 24 h average PM₁₀ concentration exceeded national ambient air quality standard (NAAQS) as specified by central pollution control board, India at both residential (Kasba) and industrial (Cossipore) areas with mean concentration of 140.1 and 196.6 μg/m³, respectively. A simultaneous meteorology study was performed to assess the influence of air masses by wind speed, wind direction, rainfall, relative humidity and temperature. The measured toxic trace metals generally showed inverse relationship with wind speed, relative humidity and temperature. Factor analysis, a receptor modeling technique has been used for identification of the possible sources contributing to the PM₁₀. Varimax rotated factor analysis identified four possible sources of measured trace metals comprising solid waste dumping, vehicular traffic with the influence of road dust, road dust and soil dust at residential site (Kasba), while vehicular traffic with the influence of soil dust, road dust, galvanizing and electroplating industry, and tanning industry at industrial site (Cossipore).     

Northern Idaho House Dust and Soil Lead Levels Compared to the Bunker Hill Superfund Site

House dust has been identified as a major exposure medium for lead (Pb) in children. High levels of Pb in soil and house dust have been recorded at the Bunker Hill Superfund Site (BHSS) in northern Idaho, an historic mining and smelting district. Soil and dust remediation at the site was required; however, regional background soil and dust Pb levels had not been well characterized. The objective of this survey was to determine background house dust Pb levels and to compare those levels with concentrations, and dust and Pb loading rates measured at the BHSS. Soil and house dust samples were collected in five towns demographically similar to the BHSS but unaffected by the mining industry. The background concentrations and loading rates were significantly lower than those observed at the site. House age was a significant factor affecting background soil and house dust Pb concentrations and loading rates.     

Paleolimnological assessment of Grove and Plow Shop Ponds, Ayer, Massachusetts, USA--a superfund site

Three sediment cores from each of severely polluted Grove and Plow Shop Ponds, Ayer, Massachusetts, USA, were dated using (210)Pb, characterized for plant macrofossil assemblages, and analyzed for H(2)O, loss-on-ignition, stable Pb isotopes, and concentrations of As, Ca, Cd, Cr, Cu, Fe, Hg, methyl-Hg, Ni, Pb, and Zn. A core from nearby kettle Spectacle Pond, Littleton, Massachusetts, was similarly characterized (except for plant macrofossil assemblages) to assess the regional air pollution signal in sediment for comparison with the six cores. Accumulation rates for metals (mass per area per year), the anthropogenic component (mass per area per year), and total accumulation of the anthropogenic component (mass per area) indicate that As, Cd, Cr, Cu, Hg, methyl-Hg, Ni, Pb, and Zn have accumulated in sediment as a consequence of point source pollution from within the drainage basins of Grove and Plow Shop Ponds. Three distinct sources of pollution are inferred. As is entering Plow Shop Pond via groundwater in the southwest. Cd, Ni, Pb, and Zn are entering the system predominantly at the eastern end of, or upstream from, Grove Pond. Pb also comes from the northwest corner of Grove Pond, the principal source of Cr, Cu, and Hg. These results are consistent with chemistry of modern surface sediments. The history of pollution extends back more than 100 years. Intra- and inter-core variability of concentrations and accumulation rates indicate that much of the pollution was likely in particulate form with little physical redistribution. Recently, concentrations and accumulation rates have generally decreased substantially for those elements present in excessive concentrations in the past. This is a consequence of accumulation of recent, less polluted sediment. In Spectacle Pond, the nearby reference lake, accumulation rates for As, Cd, Hg, and Pb, adjusted for background values and changes in sedimentation rate, increased above background starting in the late 19th century, peaked about 1980, and declined substantially to 2000. These decreases suggest that the anthropogenic (pollution) component of atmospheric deposition of these elements declined after 1980 by at least 50%(As), 80%(Cd), 80%(Hg), and 80%(Pb).