顶空气相色谱法测定北京市地下水中的氯代烃

以国家标准方法和美国环保局（EPA）方法为基础，建立用自动顶空进样器对饮用水中的氯代烃进行测定的方法，探讨了影响实验空白的因素，所拟方法的检出限为：三氯甲烷0.096μg/L、四氯化碳0.034μg/L，三氯乙烯0.049μg/L，四氯乙烯0.033μg/L。方法回收率控制在82％－106％，其相对标准偏差（RSD，n=7)小于23％，符合国际有机污染物分析的标准，并用此方法对北京市地表水、地下水进行了测定。     

浅层地下水卤代烃污染初步研究

笔者通过对某地区浅层地下水中卤代烃（三氯甲烷、四氯化碳、三氯乙烯、四氯乙烯和三溴甲烷）的测试、研究和分析，阐明了该地区浅层地下水中卤代烃污染物主要是三氯甲烷、三氯乙烯和四氯乙烯，主要污染来源是露天堆放的垃圾场、排污河渠和特殊工业企业；确定了污染源分布和包气带岩性是决定该地区卤代烃污染的两个主要因素，冲洪积扇顶部和潜水－承压水过渡带是卤代烃污染的高浓度区；最后对该地区卤代烃污染物的形成和迁移转化机理进行了初步探讨。     

长江三角洲某地区浅层地下水单环芳烃污染特征及其原因分析

本文针对长江三角洲某地区3个城市(C市、W市、S市)浅层地下水的单环芳烃进行了研究。根据研究区水样分析数据,总结出该地区单环芳烃的污染特点和分布特征,然后从研究区污染源分布、单环芳烃的挥发性、研究区降水以及包气带的防护性能等角度探讨了浅层地下水单环芳烃污染形成的原因。研究表明,该区浅层地下水单环芳烃污染呈点状分布,污染范围不大;浅层地下水单环芳烃污染相对较轻而地表水污染严重。浅层地下水单环芳烃污染特征与研究区工业企业分布、单环芳烃的挥发特性、降水以及研究区包气带防污性能密切相关。浅层地下水单环芳烃污染和工业企业分布具有很好的一致性,有机污染物高浓度的检出点均分布在污染工厂附近,无明显污染源的地段,其浅层地下水水样无有机污染物检出;各检测单环芳烃组分的亨利常数均大于1.01×102Pa·m3·mol-1,所以挥发作用是其主要迁移机理,苯的柱试验表明,苯溶液浓度从1079.0μg/L降低至6.9μg/L仅需26天;研究区包气带为河湖三角洲沉积相的淤泥质粘土,粘粒含量大,粘土矿物含量也很高,富含有机质,其含量大都在1.0%以上,此类土壤具有高的吸附能力,阻滞了污染物向浅层地下水迁移;降雨时浅层地下水中单环芳烃检出率和检出浓度都较高。4种因素综合,使得研究区浅层地下水单环芳烃呈现污染程度轻、分布零散、污染分布范围小的特点。     

大同盆地地下水中砷的形态、分布及其富集过程研究

为查明大同盆地高砷地下水的分布规律及其主要控制因素,对大同盆地典型高砷区35件地下水样进行了水化学特征及形态分析研究。结果表明,高砷地下水[ρ(As)≥50μg/L]主要存在于20~50 m的浅层地下水中,总砷质量浓度为0.56~927μg/L,主要以As(Ⅴ)形态存在。该区高砷地下水以Na-HCO3型水为主,具有明显的高pH值,高HCO-3、Fe2+、HS-质量浓度及低Eh值,低SO2-4质量浓度特征。这可能与微生物催化氧化有机碳的同时还原含铁矿物和硫酸盐的过程有关。PHREEQC模拟矿物饱和指数结果表明,高砷地下水[ρ(As)≥50μg/L]中菱铁矿均为过饱和,而低砷地下水[ρ(As)50μg/L]中均不饱和,且菱铁矿饱和指数与地下水中总砷质量浓度呈显著正相关性,该现象表明微生物还原含铁矿物生成FeCO3(菱铁矿)的过程可能是控制本区地下水中砷富集的主要因素。     

天然含钒金红石降解卤代烃实验研究

利用天然金红石光催化降解卤代烃，在1h内对三氯乙烯和四氯乙烯的降解率分别达到82．54％和94．43％，对三氯甲烷也有一定的降解作用。经电子辐射的金红石光催化活性降低，卤代烃的降解率低于原样；经加热和淬火处理的金红石样品表面钒含量增加，光催化活性提高，能将浓度400μg／L左右的三氯乙烯和四氯乙烯降解到5μg／L以下。     

生物降解作用下地下水中TCE、PCE迁移转化的数值模拟研究

根据室内三氯乙烯(TCE)、四氯乙烯(PCE)运移转化的土柱实验和研究区地下水化学特征,建立了研究区微生物作用下TCE、PCE迁移转化的数学模型,并进行了计算机数值模拟,模拟结果与实测值基本一致,表明本次研究建立的数学模型是正确的,研究区地下水中存在生物降解作用,为下一步有机污染的治理提供了科学依据。     

四氯乙烯在不同地下水环境的生物共代谢降解

四氯乙烯是地下水中常见的污染物,采用生物方法进行处理的优点是可以实现无害化、无二次污染、处理成本低。四氯乙烯只能在厌氧条件下发生还原脱氯,目前对产甲烷环境下四氯乙烯的降解研究较多,而对较弱还原环境,如反硝化、铁锰还原和硫酸盐还原环境下四氯乙烯的脱氯行为研究甚少。本文采用批实验,研究了在不同地下水环境,包括反硝化、铁还原、硫酸盐还原、混合电子受体和天然地下水环境下四氯乙烯的脱氯性能。结果表明,铁还原环境的四氯乙烯脱氯效果最好,天然地下水环境次之,四氯乙烯的去除率分别达到91.34%和84.71%,四氯乙烯很快转化为三氯乙烯,并可以进一步转化为二氯乙烯,四氯乙烯的降解符合准一级反应动力学方程。在反硝化、硫酸盐还原、混合电子受体环境,四氯乙烯的去除以挥发为主,降解只占很小的比例,且最终的降解产物只有三氯乙烯。地下水中三价铁的存在,对于四氯乙烯脱氯起促进作用;而当地下水中硝酸盐和硫酸盐的浓度较高时,四氯乙烯脱氯受到抑制。     

北京市平原区地下水有机污染时空分布特征

2007~2008年进行的北京市平原区地下水污染调查,发现该地区地下水有机污染具有检出种类多、检出率高、浓度低的特点。主要的有机污染物为三氯甲烷、四氯化碳、1,2-二氯丙烷、1,2-二氯乙烷、三氯乙烯、四氯乙烯、甲苯和苯并[a]芘。对这8种主要有机污染物的时间和空间分布特征进行了研究。研究显示,平面上,有机污染物分布广泛,主要为点状分布,局部地区集中检出。垂向上,随深度增加地下水有机污染减轻（1,2-二氯乙烷除外）。与枯水期相比,丰水期有机物检出率和浓度更高（三氯甲烷除外）,四氯化碳、三氯乙烯、四氯乙烯受枯、丰水期变化影响最小,检出重现性好,污染较严重。与2001年相比,2008年四氯化碳检出率降低,对地下水的污染有所减轻,而三氯甲烷、三氯乙烯、四氯乙烯的检出率变化较小。文章从污染源、有机物理化特性、水文地质条件等方面对有机污染时空分布特征的成因进行了阐述。     

北京市平原区地下水有机污染时空分布特征

2007~2008年进行的北京市平原区地下水污染调查,发现该地区地下水有机污染具有检出种类多、检出率高、浓度低的特点。主要的有机污染物为三氯甲烷、四氯化碳、1,2-二氯丙烷、1,2-二氯乙烷、三氯乙烯、四氯乙烯、甲苯和苯并[a]芘。对这8种主要有机污染物的时间和空间分布特征进行了研究。研究显示,平面上,有机污染物分布广泛,主要为点状分布,局部地区集中检出。垂向上,随深度增加地下水有机污染减轻（1,2-二氯乙烷除外）。与枯水期相比,丰水期有机物检出率和浓度更高（三氯甲烷除外）,四氯化碳、三氯乙烯、四氯乙烯受枯、丰水期变化影响最小,检出重现性好,污染较严重。与2001年相比,2008年四氯化碳检出率降低,对地下水的污染有所减轻,而三氯甲烷、三氯乙烯、四氯乙烯的检出率变化较小。文章从污染源、有机物理化特性、水文地质条件等方面对有机污染时空分布特征的成因进行了阐述。     

土著微生物参与下河套平原地下水中砷的还原作用

为查明土著微生物活动对高砷地下水形成的影响,利用河套平原高砷地下水中分离出的土著微生物(YH002)进行了微宇宙实验研究.实验结果表明: 高砷地下水中加入的葡萄糖提供了微生物生长所需要的碳源,微生物大量繁殖,分泌的有机酸使溶液的pH值降低.在缺氧条件下,溶液中的OD值最高达到了0.189,pH值最低为6.22;在有氧条件下,OD值最高达到了0.286,pH值最低为6.04.溶液中As(III)的初始质量浓度为74 μg/L,占总砷质量浓度的11.2%,在加入微生物和葡萄糖后,在缺氧和有氧条件下,As(III)的质量浓度分别为278 μg/L和310 μg/L,占总砷质量浓度的42%和47%.微宇宙实验说明地下水中的土著微生物能将As(V)还原成As(III).      

垃圾堆放场氯代脂肪烃对浅层地下水的污染特征初步分析

研究区是浅层地下水主要补给区，通过区内地下水监测说明，受垃圾淋滤液影响的地下水中氯代烃高值点主要集中在研究区中部；地下水中氯代烃检出值和检出率有季节性变化特征，与垃圾堆放时间和该井距垃圾场堆放场距离有密切关系，堆放时间越长，离垃圾堆放场越近，检出率、检出值越高；对地下水污染的敏感性和影响氯代烃迁移的机理方面进行了分析。     

Deterioration of groundwater quality in the vicinity of an active open-tipping site in West Malaysia

There is an urgent need for characterization of leachate arising from waste disposal to ensure a corresponding effective leachate management policy. Field and laboratory studies have been carried out to investigate the impact of municipal landfill leachate on the underlying groundwater at a site in West Malaysia. The solid waste was disposed of directly onto an unprotected natural soil formation. This situation was made worse by the shallow water table. The hydrochemical composition of groundwater in the vicinity of the site (background) is a dilute mixed cation, bicarbonate water. The high ionic balance error of ~13.5% reveals that the groundwater body underneath the site was a highly contaminated leachate rather than contaminated groundwater. Elevated concentration of chloride (355.48 mg/L), nitrate (10.40 mg/L as NO₃), nitrite (14.59 mg/L), ammoniacal-N (11.61 mg/L), sodium (227.56 mg/L), iron (0.97 mg/L), and lead (0.32 mg/L) measured downgradient indicate that the contamination plume has migrated further away from the site. In most cases, the concentration of these contamination indicators, together with the ranges of sodium percentage (66.3–89.9%) and sodium adsorption ratio (10.1–19.7%), were found to be considerably higher than the limit values of safe water for both domestic and irrigation purposes, respectively.     

Isotope analysis of nitrate pollution sources in groundwater of Dong'e geohydrological unit

As nitrate pollution in groundwater has become increasingly serious in recent years, nitrogen isotope was adopted in this paper to define its sources in a typical agricultural area of Dong'e hydrogeological unit. The results show that: Higher content of NO_3~- detected in shallow groundwater is 27.77 mg/L on average and δ15 N content ranges from 7.8‰ to 12 ‰, indicating that shallow groundwater is mainly contaminated by sewage or feces. In contrast, less NO_3~- in deep groundwater(karst water) has an average value of 12.81 mg/L and δ15 N content is between 7.2‰ and 14.3‰, which is closely related to human disturbance as mentioned above. In addition, considering relatively low groundwater quality at some monitoring sites, reasonable fertilization is a better choice in the study area to reduce nitrate source in groundwater.     

Fluoride and arsenic hydrogeochemistry of groundwater at Yuncheng basin,Northern China

High fluoride and arsenic concentrations in groundwater have led to serious health problems to local inhabitants at Yuncheng basin, Northern China. In this study, groundwater with high fluoride and arsenic concentration at Yuncheng basin was investigated. A majority of the samples (over 60%) belong to HCO₃ type water. The predominant water type for the shallow groundwater collected from southern and eastern mountain areas was Ca/Mg-Ca-HCO₃ types. For the shallow groundwater from flow through and discharge area it is Na-HCO₃/SO₄-Cl/SO₄/Cl type. The predominant water type for the intermediate and deep groundwater is of Na/Ca/Mg-Ca-HCO₃ type. According to our field investigation, fluoride concentration in groundwater ranges between 0.31 and 14.2 mg/L, and arsenic concentration ranges between 0.243 and 153.7 μg/L. Out of seventy collected groundwater samples, there are 31 samples that exceed the World Health Organization (WHO) standard of 1.5 mg/L for fluoride, and 15 samples exceeds the WHO standard of 10 μg/L for arsenic. Over 40% of high fluoride and arsenic groundwater are related to the Na-HCO₃ type water, and the other fifty percent associated with Na-SO₄-Cl/HCO₃-SO₄-Cl type water; little relation was found in calcium bicarbonate type water. A moderate positive correlation between fluoride and arsenic with pH were found in this study. It is due to the pH-dependent adsorption characteristics of F and As onto the oxide surfaces in the sediments. The observed negative correlation between fluoride and calcium could stem from the dissolution equilibrium of fluorite. The high concentration of bicarbonate in groundwater can serve as a powerful competitor and lead to the enrichment of fluoride and arsenic in groundwater. Most of the groundwater with high fluoride or arsenic content has nitrate content about or over 10 mg/L which, together with the observed positive correlations between nitrate and fluoride/arsenic, are indicative of common source of manmade pollution and of prevailing condition of leaching in the study area.     

Isotope analysis of nitrate pollution sources in groundwater of Dong’e geohydrological unit

As nitrate pollution in groundwater has become increasingly serious in recent years, nitrogen isotope was adopted in this paper to define its sources in a typical agricultural area of Dong’e hydrogeological unit. The results show that: Higher content of NO3- detected in shallow groundwater is 27.77 mg/L on average and δ15N content ranges from 7.8‰ to 12 ‰, indicating that shallow groundwater is mainly contaminated by sewage or feces. In contrast, less NO3- in deep groundwater (karst water) has an average value of 12.81 mg/L and δ15N content is between 7.2‰ and 14.3‰, which is closely related to human disturbance as mentioned above. In addition, considering relatively low groundwater quality at some monitoring sites, reasonable fertilization is a better choice in the study area to reduce nitrate source in groundwater.     

塔里木盆地南缘浅层高碘地下水的分布及成因:以新疆民丰县平原区为例

塔里木盆地位于欧亚大陆腹地,远离海洋,地下水是塔里木盆地南缘重要的供水水源,查明该区浅层地下水中碘（I-）的分布及成因至关重要.基于新疆塔里木盆地南缘的民丰县平原区44组浅层地下水水样,综合运用水化学图解法、数理统计法和GIS技术,分析潜水和浅层承压水水化学特征、碘的空间分布及高碘地下水的成因.结果表明:民丰县平原区浅层地下水中碘的富集和贫乏共存;潜水和浅层承压水I-含量范围分别为≤730 μg/L和≤183μg/L,潜水水样中缺碘水、适碘水、高碘水和超高碘水占比分别为19.4%、69.4%、5.6%和5.6%,浅层承压水水样中缺碘水、适碘水和高碘水占比分别为12.5%、75.0%和12.5%,潜水中缺碘水和超高碘水均高于承压水.从山前倾斜平原到细土平原,地下水中I-含量呈明显上升趋势.高碘水和超高碘水水化学类型主要为Cl·SO₄-Na型和Cl-Na型.除水文地质条件和偏碱性的地下水环境外,研究区潜水碘主要受强烈的蒸发浓缩作用、第四系全新统沼泽堆积物和矿物溶解沉淀的影响,浅层承压水碘主要受矿物溶解沉淀及还原环境的影响.      

长江中游故道区高碘地下水分布与形成机理

高碘地下水(碘浓度大于100μg/L)广泛分布于我国沿海地区和干旱内陆盆地,威胁近千万人口的饮水安全,但目前对湿润区河湖平原地下水中碘的分布与成因机制的认识还十分薄弱.通过采集长江中游故道区75组浅层地下水样品和7组地表水样品进行了水化学分析,查明了地下水中碘的空间分布特征,并运用主成分分析识别了碘富集的水环境要素和水...     

Arsenic Distribution Pattern in Different Sources of Drinking Water and their Geological Background in Guanzhong Basin,Shaanxi, China

To study arsenic(As) content and distribution patterns as well as the genesis of different kinds of water, especially the different sources of drinking water in Guanzhong Basin, Shaanxi province, China, 139 water samples were collected at 62 sampling points from wells of different depths, from hot springs, and rivers. The As content of these samples was measured by the intermittent flowhydride generation atomic fluorescence spectrometry method(HG-AFS). The As concentrations in the drinking water in Guanzhong Basin vary greatly(0.00–68.08 μg/L), and the As concentration of groundwater in southern Guanzhong Basin is different from that in the northern Guanzhong Basin. Even within the same location in southern Guanzhong Basin, the As concentrations at different depths vary greatly. As concentration of groundwater from the shallow wells(50 m deep, 0.56–3.87 μg/L) is much lower than from deep wells(110–360 m deep, 19.34–62.91 μg/L), whereas As concentration in water of any depth in northern Guanzhong Basin is 10 μg/L. Southern Guanzhong Basin is a newly discovered high-As groundwater area in China. The high-As groundwater is mainly distributed in areas between the Qinling Mountains and Weihe River; it has only been found at depths ranging from 110 to 360 m in confined aquifers, which store water in the Lishi and Wucheng Loess(Lower and Middle Pleistocene) in the southern Guanzhong Basin. As concentration of hot spring water is 6.47–11.94 μg/L; that of geothermal water between 1000 and 1500 m deep is 43.68–68.08 μg/L. The high-As well water at depths from 110 to 360 m in southern Guanzhong Basin has a very low fluorine(F) value, which is generally 0.10 mg/L. Otherwise, the hot springs of Lintong and Tangyu and the geothermal water in southern Guanzhong Basin have very high F values(8.07–14.96 mg/L). The results indicate that highAs groundwater in depths from 110 to 360 m is unlikely to have a direct relationship with the geothermal water in the same area. As concentration of all reservoirs and rivers(both contaminated and uncontaminated) in the Guanzhong Basin is 10 μg/L. This shows that pollution in the surface water is not the source of the high-As in the southern Guanzhong Basin. The partition boundaries of the high- and low-As groundwater area corresponds to the partition boundaries of the tectonic units in the Guanzhong Basin. This probably indicates that the high-As groundwater areas can be correlated to their geological underpinning and structural framework. In southern Guanzhong Basin, the main sources of drinking water for villages and small towns today are wells between 110–360 m deep. All of their As contents exceed the limit of the Chinese National Standard and the International Standard(10 μg/L) and so local residents should use other sources of clean water that are 50 m deep, instead of deep groundwater(110 to 360 m) for their drinking water supply.     

Hydrogeochemical contrast between two study areas of Bengal delta,India: A comparative insight to understand arsenic mobilization process in shallow aquifers

A comparative hydrogeochemical study evaluated arsenic release mechanism and differences in contamination levels in the shallow groundwater of two areas within the deltaic environment of West Bengal (i.e. Karimpur and Tehatta blocks of Nadia district) in India. Groundwaters from both the areas are Ca-Na(K)-Cl-HCO₃ type with highly reducing character (−110.16 ± 16.85 to −60.77 ± 16.93 mV). Low correlations among As, Fe, and Mn and the higher association between As and DOC are indicative of microbial decomposition of organic matter enhancing the weathering of shallow aquifer materials. Arsenic contamination in groundwater is higher in Karimpur (95 ± 81.17 μg/L) than that in Tehatta (43.05 ± 41.06 μg/L). The release mechanism of arsenic into groundwater is very complex. Low Fe (0.27–4.78 mg/L and 0.81–4.13 mg/L), Mn (0.08–0.2 mg/L and 0.03–0.22 mg/L), and SO₄²⁻ (3.82 ± 0.31 and 2.78 ± 0.40 mg/L) suggest that the mechanism of arsenic release is not a single mechanistic pathway. Clustering of redox-active parameters in the principal component planes indicate that the reductive dissolution, and/or weathering/co-precipitation of Fe/Mn-bearing minerals in the shallow aquifer sediments control the dominant mechanistic pathway of arsenic release.     

鲁北平原浅层地下水有机污染特征及污染来源分析

本文在对鲁北平原水文地质条件及污染源现状分析的基础上,对浅层地下水进行了高密度的样品采集、高精度的污染物组分测试及污染程度研究,分析研究结果表明:鲁北平原浅层地下水在部分地区受到有机物污染,污染程度总体较低,个别地区出现中度污染和重度污染。检出的有机污染物共13种,个别有机物含量高。浅层地下水污染区的分布及污染程度,与油田采油区位置及石油化工企业的分布具有相关性。