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1.
地质样品经HF-HNO_3-HCl-HClO_4溶解后,用50 g/L碳酸钠溶液浸取分离,采用紫外荧光光谱法直接测定上清液的铀含量。浸取时间选择30 min,Fe、Zn、Ca、Co、Ni、Cu和Mn等元素留在残渣中不产生干扰。方法精密度(RSD,n=12)为3．37%～7．06%,检出限为0．009μg/g(进样量100μL)。方法参加区域地球化学考核样品的测试,合格率100%,适用于土壤、水系沉积物、岩石及Fe、Zn、Ca、Co、Ni、Cu和Mn含量较高的样品中痕量铀的测定。  相似文献   

2.
在距离灌渠不同距离的包气带中钻孔取样,测定了33个土壤样品中的pH值和Ba、Cr、Cu、Fe、Mn、Ni、Pb、Zn、土壤有机质的质量分数,对这8种重金属元素在土壤样品中的质量分数进行数据统计和空间分析。结果显示:①重金属元素Cr、Cu、Ni、Pb和Zn主要来源于污水,Fe、Mn和Ba除来源于污水外,还有一部分来源于土壤母质;②Cu、Cr、Pb、Zn和Ni的空间分布差异大,变异系数可达75.22%,主要富集表层0~0.3 m深度处和黏土层(黏土层起始深度在1.2~1.5 m,厚度40 cm)中,Fe、Mn和Ba在垂向上主要呈平均分布,空间分布的变异系数为19.09%~33.10%;③包气带中重金属元素平均含量超过当地土壤背景值的3~8倍,已经在包气带表层0~0.3 m深度处和黏土层中积累,而且Ba、Cu、Fe、Mn、Ni、Zn等重金属元素已经迁移到潜水层。  相似文献   

3.
地质样品经HF—HNO3-HCl-HClO4溶解后，用50g／L碳酸钠溶液浸取分离，采用紫外荧光光谱法直接测定上清液的铀含量。浸取时间选择30min，Fe、Zn、Ca、Co、Ni、Cu和Mn等元素留在残渣中不产生干扰。方法精密度（RSD，n=12）为3．37％～7．06％，检出限为0．009μg／g（进样量100μL）。方法参加区域地球化学考核样品的测试，合格率100％，适用于土壤、水系沉积物、岩石及Fe、Zn、Ca、Co、M、Cu和Mn含量较高的样品中痕量铀的测定。  相似文献   

4.
湘江是我国重金属污染最严重的河流之一。本次工作利用X射线荧光(XRF)和电感耦合等离子质谱(ICP-MS)分析技术,对湘江竹埠港沉积物进行主量和微量元素分析。结果表明沉积物主量元素含量变化相对稳定,富集Mn O、P2O5、Fe2O3、Al2O3,亏损Ca O、Na2O。微量元素含量变化较大,亏损Ba、Sc、Mn、Sr而富集其他微量元素。对主量元素和稀土元素进行了分析,表明沉积物物源主要是由上游花岗岩风化所提供。对沉积物进行因子分析和相关性分析,表明沉积物源主要以陆源碎屑为主,并有磷灰石和软锰矿等自生副矿物,Ni、Pb、Cu可能来自人为污染源。地累积指数表明Ba为清洁无污染,重金属V、Cr、Co、Ni、Th、U为轻度污染,重金属Cu、Pb、Zn为偏中度污染,Mn为中度污染,Sc为偏重度污染。其中重金属Cr、Ni、Cu、Pb、Zn、Mn、Sc污染应引起关注。  相似文献   

5.
泉州城市表层土壤中金属元素来源分析   总被引：4，自引：0，他引：4  
采集了泉州市47个城市表层土壤样,用ICP-MS检测技术,研究了土壤中26种重金属元素的富集特征、环境风险及污染来源。富集因子结果显示,与泉州市土壤背景值相比,Li、Ni、Co、Cu、Zn、Sr、Cd、Sn、Sb、Pb、Ta在城市表层土壤中的富集因子大于1,而Ti、V、Cr、Fe、Mn、Ga、Ge、As、Rb、Y、Nb、Cs、Bi、Th、U的富集因子小于1。从功能区上看,工业区污染最为严重,其次依次为农业区、商住区、城市绿地、交通区。环境风险指数表明,泉州市城市表层土壤中重金属污染具有极高的环境风险,达到极高风险级别的样品占48.9%。采用多元统计分析方法对土壤样品中各金属元素来源进行解析,结果表明,研究区城市表层土壤中金属元素总体可分成5类：①交通运输类（Sn、Pb、Sb、Bi）;②工业因子类（Cr、Co、Ni、Fe、Mn）;③自然因子类别（Ga、Ge、Ti、V、Cu）;④混合因子类别（Zn、Cd、Sr、Th、U、Y、As、Cs、Nb、Ta、Rb）;⑤生活垃圾因子类别（Li）。  相似文献   

6.
应用X射线荧光光谱法(XRF)分析生物样品,采用传统低压粉末制样方法(压强220~440 MPa)难以将样品压制成符合测定需要的样片,样片表面粗糙,粉末容易脱落,污染XRF仪器样品室,影响仪器的长期稳定性。本文采用高压粉末制样方法在1760 MPa下压制则完全克服了低压制样的弊端,制备的样片表面光滑、致密,大幅改善了制样重现性,5次制样重现性为0.1%~2.6%,且降低了仪器的维护成本。在此基础上,建立了波长色散X射线荧光光谱法直接测定生物样品中23种主次量元素(Al、Ca、Cl、K、Mg、Na、P、S、Si、Ba、Br、Co、Cr、Cu、Fe、Mn、Ni、Pb、Rb、Sr、Ti、V、Zn)的分析方法,采用经验系数法、散射线内标法和峰背景作内标校正基体效应,大部分元素的方法精密度提高至 0.4%~11.3%,检出限为0.08~140.96 μg/g。经国家一级生物标准物质验证,表明方法准确可靠,能满足日常分析要求。  相似文献   

7.
南京市大气降尘重金属含量特征及来源研究   总被引：19，自引：0，他引：19  
文中对南京市大气降尘重金属含量水平进行了研究,从2006年12月起连续收集一年的大气降尘样品,分析了As、Cd、Cr、Cu、Hg、Mn、Mo、Ni、Pb、Se、Zn等11个元素。结果表明,与土壤背景值相比,南京市大气降尘中除Cr、Fe、Mn外的重金属含量总体明显升高。采用相关分析和主成分分析,对降尘重金属元素来源进行解析,认为有三种主要来源:一是As、Cu、Hg、Pb、Se与燃煤活动、汽车尾气排放有关。二是Cd、Ni、Zn、Mo可能与化学工业有关,但Mo还受工业活动、土壤颗粒物的影响。分析还表明,在化工业园附近的样点,这些元素含量普遍较高。三是Mn、Cr主要与土壤颗粒物有关(自然来源)。以Fe作为参考元素计算重金属的富集因子表明,自然来源的Cr、Mn具有较小的富集因子,而受工业活动影响的Cd、Pb、Se、Zn具有较大的富集因子。  相似文献   

8.
通过测定泉州湾洛阳江河口红树林区表层沉积物中酸提重金属元素含量及桐花树、秋茄两种红树植物各部位中重金属元素含量,分析了重金属元素在两红树植物不同部位的分布特征及其富集和迁移能力,并初步探讨了两种红树植物体内各重金属元素的主要来源。红树林区各采样点表层沉积物中重金属元素酸提量顺序为:FeMnZnPbCuCrN iCo,Cu和Pb的平均酸提量超过第一类海洋沉积物质量标准限值。同种元素在两种红树植物不同部位中的含量顺序一致:Cu为根枝叶;N i为叶根枝;Fe、Mn、Cr、Zn、Pb、Co为根叶枝。两种红树植物对N i、Cr、Cu、Zn、Fe、Mn的富集能力高于Co和Pb。秋茄对Cu、N i、Mn、Fe、Co的富集能力比桐花树略强些,而对Zn、Cr、Pb的富集能力则相对弱些;但两种植物对各元素的富集能力都达不到超富集植物的要求。两种植物对N i元素的富集能力都大于其他元素,且都集中在叶部,其他元素则主要集中在根部。除N i外,其余元素在两植物体内的迁移系数均小于1。桐花树中的Cr和秋茄中的Cu、Zn、Mn主要来源于林地沉积物,其他元素在两植物各部位均有不同的来源。  相似文献   

9.
徐州城市表层土壤中重金属环境风险测度与源解析   总被引：45，自引：2，他引：43  
王学松  秦勇 《地球化学》2006,35(1):88-94
研究了徐州城市表层土壤的21个样品中重金属元素富集特征,结果表明,与我国土壤元素的背景值(算术平均值)相比,表层土壤中Zn、Cd、As、Hg、Sb、Sn和Ag等元素富集程度高;Se、Sc、Ba、Bi、Pb、Cu、Ni、Cr、Mn、Mo、Be、Ga和Co等元素的富集程度较低。不同城市表层土壤中重金属元素有着不同的来源,统计分析结果表明,研究区表层土壤样品中重金属元素可分成4种类别:“自然因子”类别元素(Ti、Ga、Li、V、Co、Mn、Be和Pt);“交通因子”类别元素(Ag、Se、Sc、Pb、Cu、Zn、Cd、Br、S、Mo和Au);“燃煤因子”类别元素B(i、Cr、Hg、As、Sb和Pd)和混合源类别元素(Sn和Ba)。环境风险指数的计算结果表明,表层土壤中重金属污染具有较大的环境风险,其中属于中等环境风险级别以上的样品占近40%。  相似文献   

10.
天津市潮间带柱状沉积物中重金属的污染历史及来源判别   总被引：3，自引：0，他引：3  
利用因子分析和元素含量特征分析两种方法,对天津市潮间带的4个无扰动沉积物柱样的46个样品进行了重金属分析,并探讨了重金属的来源方式和富集原因。研究结果表明,天津市潮间带的重金属可分为3类:1)Fe、Cr、Al及Mn元素主要受环境背景值的影响,2)Hg和Cd受人为活动的影响较大,3)As、Zn、Pb、Cu及Ni受环境背景值及人类活动的双重影响,且影响大小随所在位置的不同而变化。结合210Pb和137Cs测年结果,定量确定了天津市潮间带小于0.063 mm粒级沉积物中Ni等11种重金属元素的环境背景值,并以此为基础,进一步探讨了重金属富集年代、富集量及污染历史和人类活动的关系,发现多数重金属的污染始于1910年代,并在1954年之后富集量增加。  相似文献   

11.
多壁碳纳米管固相萃取快速检测水样中铅镉铜铁   总被引：1，自引：1，他引：0  
传统的固相萃取填料应用于环境样品的重金属处理过程中,存在pH不稳定和不同极性萃取物共同萃取较为困难等方面的不足,因此寻找新型固相萃取填料显得尤为重要。本文采用多壁碳纳米管填充固相萃取柱,萃取水中金属元素铅、镉、铜和铁,采用石墨炉原子吸收光谱法测定铅和镉,电感耦合等离子体发射光谱法测定铜和铁。实验考察了多壁碳纳米管的性质、溶液pH值、洗脱溶液、样品流速以及基体效应对测定结果的影响。结果显示:溶液pH=9,1 mol/L硝酸为洗脱溶液,样品流速为2 mL/min时,外径8 nm未修饰的多壁碳纳米管有较好的萃取效率,对溶液中铅、镉、铜和铁的最大吸附容量分别为44.91、42.31、54.68和49.07 mg/g,四种元素的吸附容量均衡;钾、钠、钙、镁离子以及苯和甲苯等基质对四种金属元素的萃取影响不大。方法回收率为95.3%~99.5%,精密度(RSD,n=7)为1.2%~3.2%。本方法采用外径8 nm的多壁碳纳米管固相萃取,与传统萃取方法相比,富集效果好、回收率较高,而且操作简便、准确度高;与前人采用外径20~30 nm的多壁碳纳米管的性能相比,镉和铜的吸附容量更高,还可实现对铁的吸附,且铅、镉、铜和铁四种元素的吸附容量均衡,更适合用于检测水样中的金属元素。  相似文献   

12.
The limitation of plant growth in the polluted mediums can be used as a factor to determine of plant tolerance and the toxic effect of these mediums. In this work, the effect of Pb2+, Cd2+, Ni2+and Znsu2+ (individually) on Azolla filiculoides growth in the aqueous solution and using this method to water post treatment were studied. During 15 days the biomass the fresh Azolla with initial mass of 20 g was grown on the nutrient solution containing these metal ions, each in a concentration 4 mg/l. The presence of these ions, caused about 25%, 42%, 31% and 17% inhibition of biomass growth, respectively, in comparison to Azolla control weight which had not heavy metals. The water salinity of 1, 2 and 4 g. NaCl/l decreased the removal of these heavy metals about 4–7%, 20–24% and 40–55%, respectively. The addition of total dissolved solids (TDS) from 50 to 300 ppm. (as CaCO3) into the samples of containing heavy metals increased Azolla growth, but decreased the control Azolla growth.  相似文献   

13.
Two boreholes and ten piezometers in the Ganges flood plain were drilled and installed for collecting As-rich sediments and groundwater. Groundwater samples from the Ganges flood plain were collected for the analysis of cations (Ca2+, Mg2+, K+, Na+), anions (Cl−, NO3 −, SO4 2−), total organic carbon (TOC), and trace elements (As, Mn, Fe, Sr, Se, Ni, Co, Cu, Mo, Sb, Pb). X-ray powder diffraction was performed to characterize the major mineral contents of aquifer sediments and X-ray fluorescence (XRF) to analyze the major chemical composition of alluvial sediments. Results of XRF analysis clearly show that fine-grained sediments contain higher amounts of trace element because of their high surface area for adsorption. Relative fluorescence index (15–38 QSU) of humic substance in groundwater was measured using spectrofluorometer, the results revealed that groundwater in the Ganges flood plain contains less organic matter (OM). Arsenic concentration in water ranges from 2.8 to 170 μg/L (mean 50 μg/L) in the Ganges flood plain. Arsenic content in sediments ranges from 2.1 to 14 mg/kg (mean 4.58 mg/kg) in the flood plains. TOC ranges from 0.49 to 3.53 g/kg (mean 1.64 g/kg) in the Ganges flood plain. Arsenic is positively correlated with TOC (R 2 = 0.55) in sediments of this plain. Humic substances were extracted from the sediments from the Ganges flood plain. Fourier transform infrared analysis of the sediments revealed that the plain contains less humic substances. The source of organic carbon was assigned from δ13C values obtained using elemental analysis-isotope ratio mass spectrometry (EA-IRMS); the values (−10 to −29.44‰) strongly support the hypothesis that the OM of the Ganges flood plain is of terrestrial origin.  相似文献   

14.
The aim of this work is to evaluate the changes in groundwater chemistry in an alluvial aquifer in the Moa area. Surface and ground water, metallurgical waste and various geological material samples were collected in order to evaluate groundwater composition. The results show that the alluvial aquifer is polluted with SO42-, Mg2+and heavy metals. According to its major components in the alluvial aquifer, two types of groundwater are identified: magnesi-bicarbonated and sulphate-magnesic. Maximum SO42– and Mg2+ contents are more than 1000 mg/L, and are four times higher than the acceptable levels for human consumption of water. The high values of Cr(VI), Ni(II), Mn(II) Fe(total), SO42– and Mg2+ in alluvial aquifers are due to polluted recharge from metallurgical waste from the tailing dam. This recharge is favoured by the preferential flow due to desiccation cracks in metallurgical waste. Geochemical modelling showed that potentially toxic heavy metals might exist largely in the forms of MSO42– and M2+ in pore water of SAL metallurgical waste. All samples were supersaturated in goethite and hematite. Results from batch testing indicate that the heavy metals have two origins: natural, due to the existing ultramaphic rocks and laterites, and anthropogenic, by metallurgical waste rich in sulphate and (oxy)hydroxide minerals. These results highlight the need to locate and evaluate a new water source to supply the population of the city of Moa.  相似文献   

15.
This study investigated the effect of a pine/oak forest canopy on rainfall chemistry in the Qinling Mountains. The area is an important water source for China’s North-to-South Water Transfer Project. Rainfall and throughfall samples were collected at the Huoditang Natural Forest in 1999, 2004, and 2009. Analyses of the samples indicated that the forest canopy had several important effects on rainfall chemistry. Rainfall pH generally increased as water passed through the canopy. On average, the rainfall pH increased by 0.54 pH units. The canopy’s effect declined after deciduous trees lost their leaves late in the sampling season. Rainfall NO3 ? concentrations generally declined as water passed through the forest canopy, but PO4 3? concentrations generally increased. On average, rainfall NO3 ? concentration declined by 0.135 mg/L as it passed though the forest canopy and PO4 3? increased by 0.85 mg/L. The forest canopy had a mitigating effect on the base cation content of throughfall. Specifically, K+, Na+, Ca2+ and Mg2+ were leached from the canopy when the concentration of these cations in rainfall was low. In contrast, K+, Na+, Ca2+ and Mg2+ were absorbed by the canopy when the concentration of these cations in rainfall was high. The pH of rainfall, as well as its K+, Ca2+ and Mg+ concentration, influenced the effect of the forest canopy on the base cation content of throughfall. The concentration of Cd, Pb, and Zn in rainfall generally decreased as water passed through the forest canopy, but the concentration of Fe in rainfall generally increased. The Cd concentration decreased by an average of 3.938 μg/L, the Pb concentration decreased by an average of 8.457 μg/L, and the Zn concentration decreased by an average of 0.986 mg/L. The Fe concentration increased by an average of 0.009 mg/L. The canopy’s ability to absorb Cd declined after several rainfall events in which rainfall Cd concentrations were relatively high.  相似文献   

16.
The hydrogeochemistry of groundwater and environmental aspects of the Tanjero area (Sulaimani City, Kurdistan region, Iraq) were investigated statistically. Correlation analysis and cluster analysis revealed several indicators for the source of contaminations. The hydrochemical classification of the water samples determined Ca2+, Na+, and Mg2+ as dominant ions and K/Rb and Na/Cl ratios indicated water–rock interactions with several minerals (e.g., silicate and carbonate minerals). Sr, Ca, Mg, Rb, and K (1757, 117, 29.8, 7.23, and 10.1 μg/L, respectively) in the water samples correlate with each other and show higher concentrations in the wells around scrape and dump sites than the other wells. The water samples were classified according to a redox classification as well, and aerobic and intermediate anaerobic categories were recognized with regard to the reduction of dissolved oxygen and Mn (VI) ions with organic matter in the groundwater. Mn exceeds drinking water standards.  相似文献   

17.
The aim of this study was to do a preliminary assessment of the hydrochemical and microbial groundwater quality of the West Thrace region. Forty samples of groundwater collected from Edirne (Site 1) to Gelibolu (Site 2) were assessed for their suitability for human consumption. As3− was non-detectable in all the groundwater and Zn2+, Pb2+, F−, Cu2+, NH4+, Cn− PO43− and Cl− were all below their respective European Union drinking water directive (EU-DWD) and Turkish food codex-drinking water directive (TFC-DWD). Maximum Acceptable Concentrations (MAC) Ni2+, Pb2+, Cd2+, Mg2+, Mn2+, and Ca2+ levels were detected in upper maximum acceptable concentrations 77.5, 42.5, 35.0, 50.0, 50.0, and 32.5% of the groundwater samples, respectively. However, in terms of Cr3+, Ni2+ and Pb2+, the differences between groundwaters of Sites 1 and 2 were significant (p < 0.05). Eight water samples (20%) had HPC exceeding the EU and Turkish water directive limit 20 CFU (Colony Forming Unit)/ml in drinking water and the maximum bacteria count recorded was 44 CFU/ml. Total coliforms, thermotolerant coliforms, E. coli, Enterococcus spp., Salmonella sp., Staphylococcus spp. and P. aeruginosa were detected in 25, 17.5, 15, 47.5, 15, 27.5, and 15% of the groundwater samples, respectively. Furthermore, heavy metals and trace elements were found after chemical analyzes in most samples. The pollution of groundwater come from a variety of sources, Meric and Ergene rivers, including land application of agricultural chemicals and organics wastes, infiltration of irrigation water, septic tanks, and infiltration of effluent from sewage treatment plants, pits, lagoons and ponds used storage.  相似文献   

18.
The Kandy lake, situated in the heart of Sri Lanka's second largest city with a population of nearly 120,000, has been monitored to probe the extent of heavy metal pollution. Although the lake is a source of drinking water to the city, a large number of effluent canals drain into the lake carrying a continuous flow of industrial and domestic waste matter. A total of 66 surface water samples were analyzed for their Fe2+, total Fe, total V, SO 4 2− , Cd2+, and Pb2+ contents. Pb and Cd were found in high concentrations averaging 150 μg/l and 77 μg/l, respectively, and exhibit a marked positive correlation with each other (r=+0.94). Vehicular emissions and industrial waste matter contribute largely to the Pb and Cd contents of the lake, the anthropogenic influence outweighing the contributions made by geological materials. All field observations and laboratory experiments indicate a tendency of the Kandy Lake towards eutrophicity.  相似文献   

19.
邵坤  赵改红  赵朝辉 《岩矿测试》2019,38(6):715-723
磁铁矿是一种绿色廉价的矿物材料,对水体中重金属离子具有良好的吸附性,但吸附容量低,选择性差,易团聚,通过改性可以克服该缺点并提高其吸附性能。本文以腐植酸为改性剂,采用常温水相反应制备了腐植酸改性磁铁矿吸附材料。通过傅里叶红外光谱(FTIR)、扫描电镜(SEM)和X射线光电子能谱(XPS)表征研究其表面形貌和微观结构。采用静态平衡实验考察了pH、吸附时间等因素对铅、镉吸附性能的影响,探讨了吸附动力学规律,拟合了吸附等温线。结果表明:腐植酸上的羧基、羟基被成功地接枝到了磁铁矿表面。在室温下,溶液初始pH对Pb~(2+)的吸附率几乎无影响,对Cd~(2+)的影响较大,当pH=7时,Pb~(2+)和Cd~(2+)吸附率均达到了95%。对初始质量浓度为10mg/L的Pb~(2+)、Cd~(2+)最佳吸附平衡时间为360min,吸附过程符合准二级动力学方程。吸附等温线实验得到的竞争吸附顺序为Pb~(2+)Cd~(2+),由Langmuir等温吸附模型得到Pb~(2+)、Cd~(2+)饱和吸附容量分别为39.27mg/g、28.95mg/g,显著大于磁铁矿的饱和吸附容量,表明磁铁矿经腐植酸改性后增强了对水中铅镉的吸附能力。  相似文献   

20.
样品测试是研究岩溶区水工环问题的重要手段。岩溶区交通不便利、样品运输困难以及测试单位处理样品不及时,导致样品测试存在不同程度的滞后,现有研究还不能有效解释"测试滞后"对岩溶水样性质有何影响。为此,本文以云南宣威市一典型岩溶泉水为研究对象,通过离子色谱仪、原子发射光谱仪等测试手段,对同一时间点采集的泉水样品按照时间序列对K+、Na+、Ca2+、Mg2+、Cl-、SO2-4、HCO-3、pH、NO-3、CO2(fs)共10项指标进行对比实验,探讨"测试滞后"对岩溶水样性质的影响。结果表明:岩溶水样放置过程中,各指标A类标准不确定度为0. 02～1. 83,HCO-3、Ca2+不确定度值显著高于其他指标; Shapiro-Wilk正态性检验结果显示pH、K+、Mg2+、Cl-、NO-3服从正态分布;随着时间变化,各指标相对偏差变化范围0%～57. 38%,其中pH、Ca2+、SO2-4、NO-3的相对偏差在允许误差范围之内; 10项指标均值含量与变异系数总体呈显著负相关性(Spearman相关系数为-0. 709,P 0. 05),变异系数为Na+ K+ CO2(fs) Mg2+ Cl-SO2-4 Ca2+ HCO-3 p H NO-3,揭示测试滞后对不同指标的影响程度不同,其中对质量分数低的指标影响尤为突出。在整个实验期间内,水样水质变化可分为5个阶段:以各项指标未出现明显变化的初期稳定阶段(0～3d),以Na+、K+、Mg2+三项指标出现显著变化的初步变化阶段(3～5d),以多项指标发生较为显著变化的混合变化阶段(5～17d),以微生物作用为主的细菌潜在影响阶段(17～35d),以水质趋于稳定的相对平衡阶段(35～75d),其中"细菌作用"和"碳酸平衡作用"是岩溶水样放置过程中存在的两个重要作用机制。研究结果可为提高岩溶水样测试质量提供科学指导。  相似文献   

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