原子吸收光谱法测定多维元素药片中矿物质含量

采用原子吸收光谱法测定了多维元素药片中矿物质含量。样品用硝酸消解,用火焰原子吸收法测定钙、镁、钾、铜、铁、锰,用石墨炉原子吸收法测铬和镍。方法灵敏可靠,测量相对标准偏差<2.4%,回收率在90%～100%之间,能满足药品检测要求。     

南通市某钢丝绳行业集中区降尘中重金属污染状况评价

针对南通市钢丝绳行业集中区重金属污染问题,分析降尘中的铅、镉、铬、铜、镍、铁、锌、锰等重金属含量,并采用污染指数法和地累积指数法对降尘中重金属污染状况进行评价。结果表明,该集中区降尘中重金属污染程度依次为Zn>Pb>Cd>Cu>Fe>Mn>Ni>Cr,铅、锌为主要污染因子,铅、锌污染级别均处于重污染级别。     

密闭微波消解 ICP- AES 法测定大气颗粒物中金属元素

采用过氯乙烯滤膜采集、密闭微波消解、电感耦合等离子发射光谱法测定大气颗粒物中铅、镍、铬、铜、铁、锌、锰、钡、镉,优化了试验条件.方法线性良好,各元素的检出限在0.001 mg/L～0.01 mg/L之间,滤膜样品测定的RSD为0.6%～2.9%,加标回收率为96.0%～105%.     

用火焰原子吸收法测定镀铬泥渣中的铁、镍、铜、锌、铅

我们曾对镀铬泥渣中铬的原子吸收测定进行了研究,本文重点研究镀铬泥渣中Fe、Ni、Cu、Zn、Pb测定时共存元素的干扰及其消除方法。 实验证明,大量Ni、Si的存在严重干扰铁的测定,大量Cu的存在严重干扰Ni的测定。采用标准加入法以消除Ni对Fe的干扰;采用沉淀法,萃取法分离铁与镍;在标液中加入等量铜来消除大量铜对测定镍的干扰,都难免繁琐费时。本文采用加入十二烷基硫酸钠或柠檬酸作干扰抑制剂,消除了大量铜对镍及大量硅对铁、锌测定的干扰;用降低乙炔流量,提高火焰温度的方法消除了二倍量的镍对铁测定的干扰,拟定了用火焰原子吸收法,不经分离直接测定镀铬废水处理后的泥渣中铁、镍、铜、锌、铅的测定程序。样品分析精密度均小于±4％,铁、镍、铜、铅的标准加入回收率为96—106％,锌为90—115％,用于实际样     

图们市区大气PM10中7种重金属的监测与分析

2007年6月至2008年3月分4个季节在图们市区利用大气综合采样器采集4个监测点位的大气PM₁₀样品,用硝酸-双氧水湿法消解,火焰原子吸收分光光度法检测样品中铬、锰、铁、铜、锌、镉、铅7种重金属含量,并对7种重金属元素的时空变化规律进行研究。结果表明:图们市大气PM₁₀中重金属含量由高到低的顺序是铁>锌>锰>铅>铬>铜>镉,铁的含量明显高于其他重金属含量。铅的年平均值为1.436 μg/m³,超出现行《环境空气质量标准》(GB 3095—1996)规定的浓度限值。重金属的季节性变化规律比较明显,冬季Cr、Cu、Zn、Pb的含量明显高于其他3个季节。区域性功能则不明显,在4个监测点位中7种重金属含量的变化不是很大。7种重金属含量年平均值的日变化规律也不是很明显,说明重金属来源除了天然源外,主要来自于煤和汽油燃烧过程中排放的飘尘。     

西南某省14种尾矿重金属浸出量及总量分析

研究中国西南某省不同类型尾矿的重金属浸出量及总量,为尾矿的污染防范、环境管理和综合利用提供参考和建议。采集了14种类型共164个有代表性尾矿进行浸出毒性试验,并分析其中79个典型尾矿样品的9种重金属含量,以评估其污染风险和综合利用价值。结果表明,有5种类型共7个样品出现浸出毒性超标,分别为铅锌矿、镍矿、银矿、铁矿、锰矿,总体超标率为4.3%。超标元素分别为砷、镉、锌、铅、铜、镍等6种元素,最大超标倍数分别为砷18.3倍、锌4.8倍、镉3.0倍、铅0.56倍、铜0.32倍、镍0.16倍;尾矿含有较多重金属,其中砷、锌、铅、铜含量较高,最高分别达到11.75%、2.60%、1.01%、0.29%,不同类型尾矿其重金属含量各有不同,铅锌矿尾矿的重金属总量最高。总体上,该省绝大多数尾矿为普通固废,少部分为危险废物,砷、镉、锌、铅、铜、镍等6种元素存在污染风险,其中砷元素是最主要污染物;尾矿由于重金属含量较高而有一定的综合利用价值。     

湛江南桥河、北桥河水重金属含量及分布的研究

通过硝酸-过氧化氢微波消解样品,采用ICP-AES法测定了河水中锌、铅、镉、砷、镍、铁、铬、铜等重金属元素的含量,并分析了这些重金属元素在不同河段、不同水期含量的分布情况。测定结果的RSD<9%,加标回收率在86.0%~103.4%之间,检出限在0.832~2.42μg/L之间,该方法快速、稳定、效果较好。     

水稻重金属含量与土壤质量的关系

根据“淮安市绿色食品基地调查以及相关研究”课题资料 ,分析了水稻中重金属含量与其土壤质量的关系。结果表明 ,重金属含量在水稻中的分布是 :根 >茎叶 >籽粒 ;水稻籽粒对重金属的吸收特点因其元素不同而差异较大 ,重金属元素被水稻糙米吸收的程度为 :砷 <镉 <汞 <铅 <锰 <铬 <铜 <锌 ;在糙米中检出的重金属铜和铬的含量与土壤中铜和铬的含量呈显著性相关关系 ,铅、锌、锰的含量与土壤中铅、锌、锰的含量相关关系不显著     

ICP-MS法同时测定地表水中18种金属元素

以115In-103Rh为双内标校正系统,采用电感耦合等离子体质谱法同时测定地表水中铜、锌、硒、砷、汞、镉、铅、铁、锰、钼、钴、铍、锑、镍、钡、钒、钛、铊等18种金属元素,优化了测量同位素、内标元素等试验条件。18种金属元素在0μg/L～100μg/L范围内线性良好,检出限为0.006μg/L～0.123μg/L,标准样品的测定值均在保证值范围内,平行测定的RSD为1.7%～4.2%,实际水样加标回收率为89.0%～100%。     

菏泽市不同类型村庄土壤主要无机元素的监测与评价

为揭示土壤主要无机元素积累成因,制定科学防控措施,以菏泽市养殖型、蔬菜型、粮食型、工业型4种类型村庄为研究对象,分析了11个典型村庄8种土壤主要无机元素含量、分布特征及污染风险。结果表明,土壤镉、汞、砷、铅、铬、铜、镍、锌的质量分数分别为0. 01～0. 53、0. 002～0. 145、5. 51～15. 20、17. 6～75. 8、14. 5～69. 9、13. 3～33. 8、18. 8～46. 9、41. 5～96. 4 mg/kg。蔬菜型村庄镉、汞、铅元素含量最高;粮食型村庄铬、铜、镍含量最高;养殖型村庄砷、锌元素含量最高;工业型村庄铬、铜、镍元素含量较高,其余元素的含量都较低。各主要无机元素平均值均未超过农用地土壤污染筛选值,但除汞外,均超过了黄河故道区域土壤环境背景值,尤以镉最显著。     

Heavy metal contamination in water, soil, and vegetables of the industrial areas in Dhaka, Bangladesh

Concentrations of Cu, Zn, Pb, Cr, Cd, Fe, and Ni have been estimated in soils and vegetables grown in and around an industrial area of Bangladesh. The order of metal contents was found to be Fe > Cu > Zn > Cr > Pb > Ni > Cd in contaminated irrigation water, and a similar pattern Fe > Zn > Ni > Cr > Pb > Cu > Cd was also observed in arable soils. Metal levels observed in different sources were compared with WHO, SEPA, and established permissible levels reported by different authors. Mean concentration of Cu, Fe, and Cd in irrigation water and Cd content in soil were much above the recommended level. Accumulation of the heavy metals in vegetables studied was lower than the recommended maximum tolerable levels proposed by the Joint FAO/WHO Expert Committee on Food Additives (1999), with the exception of Cd which exhibited elevated content. Uptake and translocation pattern of metal from soil to edible parts of vegetables were quite distinguished for almost all the elements examined.     

Chemical fractionation of heavy metals in urban soils of Guangzhou, China

Knowledge of the total concentration of heavy metals is not enough to fully assess the environmental impact of urban soils. For this reason, the determination of metal speciation is important to evaluate their environment and the mobilization capacity. Sequential extraction technique proposed by the former European Community Bureau of Reference (BCR) was used to speciate Cd, Cu, Fe, Mn, Ni, Pb, and Zn in urban soils from Guangzhou into four operationally defined fractions: HOAc extractable, reducible, oxidizable, and residual. The Cu, Fe, Ni, and Zn were predominately located in the residual fraction, Pb in the reducible fraction, and Cd and Mn within the HOAc extractable fraction. The order of Cd in each fraction was generally HOAc extractable > reducible > residual > oxidizable; Cu and Fe were residual > reducible > oxidizable > HOAc extractable; Mn was HOAc extractable > residual > reducible > oxidizable; Ni and Zn were residual > reducible > HOAc extractable > oxidizable; and Pb was reducible > residual > oxidizable > HOAc extractable. Cadmium was identified as being the most mobile of the elements, followed by Mn, Zn, Ni, Cu, Pb and Fe. Iron–Mn oxides can play an important role in binding Cd, Cu, Ni, Pb, and Zn and in decreasing their proportion associated with the residual fraction in the soils. With total concentrations of Cd, Cu, Ni, Pb, Zn, and Mn increase, these metals more easily release and may produce more negative effects on the urban environment.     

Heavy metal speciation in solid-phase materials from a bacterial sulfate reducing bioreactor using sequential extraction procedure combined with acid volatile sulfide analysis

Heavy metal mobility, bioavailability and toxicity depends largely on the chemical form of metals and ultimately determines potential for environmental pollution. For this reason, determining the chemical form of heavy metals and metalloids, immobilized in sludges by biological mediated sulfate reduction, is important to evaluate their mobility and bioavailability. A modified Tessier sequential extraction procedure (SEP), complemented with acid volatile sulfide (AVS) and simultaneous extracted metals (SEM) measurements, were applied to determine the partitioning of five heavy metals (defined as Fe, Ni, Zn and Cu, and the metalloid As) in anoxic solid-phase material (ASM) from an anaerobic, sulfate reducing bioreactor into six operationally defined fractions. These fractions were water soluble, exchangeable, bound to carbonates (acid soluble), bound to Fe-Mn oxides (reducible), bound to organic matter and sulfides (oxidizable) and residual. It was found that the distribution of Fe, Ni, Zn, Cu and As in ASM was strongly influenced by its association with the above solid fractions. The fraction corresponding to organic matter and sulfides appeared to be the most important scavenging phases of As, Fe, Ni, Zn and Cu in ASM (59.8-86.7%). This result was supported by AVS and SEM (Sigma Zn, Ni and Cu) measurements, which indicated that the heavy metals existed overwhelmingly as sulfides in the organic matter and sulfide fraction. A substantial amount of Fe and Ni at 16.4 and 20.1%, respectively, were also present in the carbonate fraction, while an appreciable portion of As (18.3%) and Zn (19.4%) was bound to Fe-Mn oxides. A significant amount of heavy metals was also associated with the residual fraction, ranging from 2.1% for Zn to 18.8% for As. Based on the average total extractable heavy metal (TEHM) values, the concentration of heavy metals in the ASM was in the order of Cu > Ni > Zn > Fe > As. If the mobility and bioavailability of heavy metals are assumed to be related to their solubility and chemical forms, and that they decrease with each successive extraction step, then the apparent mobility and bioavailability of these five heavy metals in ASM increase in the order of Cu < As < Ni < Fe < Zn. The SEM/AVS ratio was less than one in eight replicate ASM samples, indicating that the ASM was non-toxic with regards to having a low probability of bioavailable metals in the pore water.     

Assessment of heavy metal toxicants in the roadside soil along the N-5, National Highway, Pakistan

The assessment of the toxicants in roadside soil on regular basis has become extremely essential with the increase in awareness for the metal toxicity in the environment. The present study investigates the presence of toxic metals along National Highway (N-5), Pakistan. Averages of about 1.3 million per month of automobile vehicles ply on this route. Lead (Pb), zinc (Zn), copper (Cu), nickel (Ni), cadmium (Cd), cobalt (Co), manganese (Mn), mercury (Hg), and iron (Fe) were analyzed by atomic absorption spectrophotometry in roadside soil at the nine selected locations along the highway. Strong Pearson correlations (α = 0.05) were found between Pb and Zn (r(2)?= 0.887), Fe and Mn (r(2)?= 0.880), Hg and Cd (0.864), Cu and Zn (0.838), and Cu and Pb (0.814). The correlation between the elemental compositions of the main automobile components revealed vehicular traffic as the main non-point source of roadside soil pollution. Extremely high level of mercury, 144.05 mg kg(-1), was found at S5. It was revealed that the unregulated incineration and dumping sites of hazardous waste material along N-5 were also responsible for these contaminations. Multivariate analysis on the obtained data also disclosed the same interpretation. Cluster analysis of the data grouped Pb, Zn, and Cu at 85.23% similarity, whereas, Cd, Hg, and Ni were grouped at 78.75% similarity basis. The findings need swift action against the root cause of soil pollution.     

Spatial distribution of trace metals (Cd, Pb, Hg, Cu, Zn, Fe and Mn) and oligo-elements (Mg, Ca, Na and K) in surface sediments of the Gulf of Tunis (Northern Tunisia)

The purpose of this paper is to evaluate the levels and spatial distribution of trace metals (Cd, Pb, Cu, Hg, Zn, Fe, and Mn), oligo-elements (Mg, Ca, Na and K), total organic carbon (TOC), and total nitrogen (TN) in the fine fraction of surface sediments collected from 38 stations in Gulf of Tunis (Mediterranean Sea, Northern Tunisia) between 2004 and 2005. The results showed that metals, oligo-elements, TOC, and TN concentrations in the sediments of the Gulf of Tunis are generally low compared to those found in other similar coastal marine areas. The spatial distribution of metals showed areas of major accumulation of Pb, Cd, Cu, Fe, and Zn in the central area of the Gulf and near the Mejerda River. The marine currents are influencing factors on metal accumulation in sediments. The principal component analysis applied to our elemental analytical results showed that there is a positive correlation between Fe, Zn, Cu, and Pb. These metals have a stronger affinity with site connection in the sediments than Ca and Mn.     

Environmentally safe sewage sludge disposal: the impact of liming on the behaviour of Cd, Cr, Cu, Fe, Mn, Ni, Pb, and Zn

Dewatered sewage sludge containing relatively high total concentrations of Cr (945 micrograms ml-1), Cu (523 micrograms ml-1), Ni (1186 micrograms ml-1) and Zn (2950 micrograms ml-1) was treated with quicklime and sawdust for sludge disinfection and post-stabilisation. The mobility of the heavy metals in the sludge samples was assessed by applying a modified five-step Tessier sequential extraction procedure. Water was added as a first step for estimation of the proportion of the easily soluble metal fractions. To check the precision of the analytical work the concentrations of heavy metals in steps 1-6 of the extraction procedure were summed and compared to the total metal concentrations. The mass balance agreed within +/- 3% for Cd, Cu, Cr, and Zn and within +/- 5% for Ni, Pb, Fe and Mn. Data from the partitioning study indicate that in the lime-treated sludge at a pH of 12 the mobility of Cu and Ni notably increased with the solubilisation of these metals from their organic and/or carbonate and Fe and Mn oxide and hydroxide fractions, respectively. Liming slightly decreased the proportion of other heavy metals in the easily soluble fractions while its impact on the partitioning between other sludge phases was almost insignificant. Due to the increased solubility of Ni and Cu as well as potential Cr oxidation at high pH, liming cannot be recommended for sludge disinfection. Addition of sawdust did not change the heavy metal partitioning.     

Assessment of heavy metal contamination in Candarli Gulf sediment, Eastern Aegean Sea

Concentrations of selected heavy metals (Fe, Mn, Ni, Cu, Zn, Pb, Hg, Cr, Al, and As) in surface sediments from 18 stations in the Candarli Gulf were studied in order to understand current metal contamination due to urbanization and economic development in Candarli region, Turkey. The sediment samples were collected by box corer in Candarli Gulf in 2009 to assess heavy metal pollution. Heavy metal concentrations in surface sediment varied from 1.62% to 3.60% for Fe, 0.38?C2.53% for Al, 173?C1,423 for Mn, 8?C100 for Ni, 3?C46 for Cu, 55?C119 for Zn, 16?C138 for Pb, 0.2?C6.3 for Hg, 16?C71 for Cr, and 11?C37 mg kg^???1 for As. This study showed that the concentrations of Mn, Ni, Zn, Pb, Hg, and Cr in the surface sediment layers were elevated when compared with the subsurface layers. Both metal enrichment and contamination factors show that Hg, Zn, and Pb contamination exists in the entire study area and contamination of other metals is also present in some locations depending on the sources.     

Speciation and ecological risk of heavy metals in intertidal sediments of Quanzhou Bay, China

The chemical speciation of nine heavy metals in intertidal sediments from Quanzhou Bay was determined using a modified sequential extraction procedure, proposed by the Commission of the European Community Bureau of Reference. The results show that Mn presents the highest percentage in the acid-soluble fraction, and Pb and Cu present the highest percentages in the reducible fraction. The highest percentages of Fe, V, Cr, Ni, Zn, and Co were found in the residual fraction. The mobility order of the heavy metals studied on the basis of the nonresidual content of the elements is Mn > Pb > Cu > Co > Zn > Ni > Cr > V > Fe. The assessment on potential ecological risk indices of some heavy metals indicates that Zn, Ni, and Cr show moderate contamination, while Cu and Pb show slighter contamination. On the whole, the comprehensive potential ecological risk index of Cu, Zn, Ni, Cr, and Pb in the sediments presents moderate degree.     

Levels of lead, cadmium, copper, iron, and zinc in deciduous teeth of children living in Irbid, Jordan by ICP-OES: some factors affecting their concentrations

The aim of this study was to measure the concentrations of lead (Pb), cadmium (Cd), copper (Cu), iron (Fe), and zinc (Zn) in deciduous teeth from children living in Jordan and to investigate the affecting factors. Deciduous teeth samples (n?=?320, without fillings) were collected from 5- to 12-year-old children and analyzed for Pb, Cd, Cu, Fe, and Zn using inductively coupled plasma–optical emission spectrometry. A questionnaire was used to gather information on each child, such as sex, age, tooth type (incisors, canines, and molars), tooth position within the mouth (upper or lower jaw), caries status, presence of amalgam fillings inside the mouth, type of drinking water (tap water, home purified water, and plant purified water), and zone of residence (close to or far from heavy traffic roads). The mean concentrations of Pb, Cd, Cu, Fe, and Zn were 30.26, 0.55, 6.23, 34.72, and 128.21 μg/g, respectively. Our results indicate that there is a clear relation between the concentrations of the metals analyzed in this study and tooth type, tooth position within the mouth, caries status, presence of amalgam fillings inside the mouth, and type of drinking water. No significant differences in the concentrations of the five metals analyzed were observed due to sex. Our results also show that no significant difference among Pb, Cd, Cu, Fe, and Zn concentrations and age among the ages of 5–6, 7–8, 9–10, and 11–12, except for Pb, which decreases at age 11–12.     

An assessment of metal contamination risk in sediments of Hara Biosphere Reserve,southern Iran with a focus on application of pollution indicators

The aim of this study was to assess the pollution status of metals in sediments of Hara Biosphere Reserve using pollution indicators. For this purpose, sediment samples from nine locations were collected and characterized for metal content (Pb, Cr, Zn, Cu, and Fe) using the total digestion technique. Comparison of metal concentrations with that of sediment quality guidelines (SQGs) demonstrated no association with negative biological effects for Cu and Zn, while the values of Pb and Cr mainly illustrated to have association with negative biological effects. The results of the geo-accumulation index (I _geo) indicated no contamination for Cr, Cu, Zn, and Fe, while the values of Pb demonstrated to have moderate contamination based on I _geo values. The analysis of the enrichment factor (EF) showed no enrichment for Cu and Zn and minor enrichment for Pb and Cr. Similar results were also found for quantification of contamination (QoC) analysis, where the values of Cu and Zn demonstrated to have a geogenic source of contamination, while the values of Pb and Cr mainly illustrated to have an anthropogenic source of contamination. According to EF and QoC calculations, the values of Cu and Zn were derived mainly from natural processes and exposure of material from the earth’s crust, while the values for Pb and Cr were enriched by anthropogenic activities. The results of the contamination factor (C _f ⁱ ) demonstrated low contamination levels for Fe, Cr, Zn, and Cu and moderate contamination levels for Pb. The pollution load index (PLI), showing the overall contamination of metals, demonstrated moderate pollution status in the study area.