离子色谱在砷化物形态分析中的应用

砷的分析方法最初有光度法、原子吸收光谱法和极谱法等，但这些方法仅能用于总砷，不能用于砷的形态分析．因而又发展了电感耦合等离子体质谱法(ICP-MS)、离子色谱法(IC)、气相色谱法、气相色谱-原子吸收光谱联用、液相色谱-质谱联用、离子色谱-电感耦合等离子体质谱、离子色谱-原子吸收／发射光谱联用技术等．由于砷化物在水中多以离子形式存在，采用离子色谱法能同时分析不同形态的砷离子．同时，采用电感耦合等离子体质谱及原子吸收光谱测定砷化物具有较高的灵敏度，因此，离子色谱及离子色谱与电感耦合等离子体质谱、原子吸收／发射光谱的联用技术在砷化物的形态分析中得到了较多的应用^[1-8]。     

利用‘树皮''进行大气污染历史监测的新采样方法

1　IntroductionBesidestheusualsamplingmethods,theconcentrationsofpollutantsintreebarkandtreebarkpockethavebeenproposedforevaluatingthedegreeofairpollutionofpresentandinthepast[1— 4 ].Inthisstudytheconcentrationsofleadandcadmiumintheoutertreebarksofredbud…     

Assessment of potentially toxic elements in Swiss chard and sediments of Akaki River,Ethiopia

For the determination of 15 potentially toxic elements (V, Cr, Fe, Mn, Co, Ni, Cu, Zn, As, Se, Ag, Cd, Sn, Hg, and Pb) in plant and sediment samples of the Akaki River, Ethiopia, inductively coupled plasma–mass spectrometry, inductively coupled plasma–optical emission spectrometry, and a RA-915+ mercury analyzer were applied. Sediment and plant samples were mineralized using a closed-vessel microwave-assisted digestion system. The elemental concentrations varied considerably in plant and sediment samples. The minimum concentration was observed for known toxic elements (As, Hg, and Cd) while the highest concentration was observed for the elements of relatively low toxicity Zn, Mn, and Fe. The concentration of Cr, Fe, Pb, Zn, and As in Swiss chard surpassed the maximum permissible levels at specific sites. At some of the sites, the sediment quality guidelines are surpassed for Cu, Zn, and Pb.     

Metals and organic pollutants in snow surrounding an iron factory

To estimate air pollution snow samples were collected in March 2001 at six sites in the vicinity of the Kostomuksha factory in Karelia. Seventy-two chemical elements and more than 200 individual organic compounds were identified by inductively coupled plasma mass spectrometry (ICP-MS) and gas chromatography mass spectrometry (GC-MS). It was found that the levels of Li, B, Al, Fe, Ni, Cu, Zn, Hg, Mn, Mo as well as hydrocarbons, phthalates and phenols exceeded the existing maximum allowable concentrations. A list of toxicants emitted with the factory exhausts and a list of priority pollutants for Kostomuksha were compiled. The impact of the exhausts of the Kostomuksha factory on the environment in Finland is relatively small. Electronic Publication     

Comparative chemical analysis of some traditional Omani-made kohl

Fourteen different types of Omani-made kohl were collected from different locations in Oman. The kohl samples were analyzed using different analytical techniques including X-ray powder diffraction, scanning electron microscopy, energy-dispersive X-ray microanalysis, and inductively coupled plasma mass spectroscopy after sample digestion. The results show that six kohls (kohls 1–6) are mineral-based, four of which, namely lasif, cold ethmid, hot ethmid, and original ethmid, contain very high levels of Pb (basically galena). The other two kohls (red ethmid and black ethmid) contain mostly iron (hematite, magnetite, and goethite). The other kohl samples (kohls 7–14) are basically amorphous carbons, one of which is made by charring date stones while the rest are basically soot collected from burning different materials. Compared to the results obtained by inductively coupled plasma mass spectroscopy, energy-dispersive X-ray microanalysis yielded higher concentrations of major elements while some minor elements were not detected; this is probably related to some limitations in the latter technique. Based on this study, carbon-based kohls possess much lower levels of toxic elements than mineral-based kohls; consequently, the former can be considered as the less hazardous kohls. However, concerns about the use of soot in cosmetics are rising because of the presence of some carcinogenic compounds such as polyaromatic hydrocarbons in soot.     

电感耦合等离子体质谱法在土壤环境监测中的应用及进展

电感耦合等离子体质谱（ICP-MS）作为高灵敏度的分析仪器,已被许多国家应用于环境监测中.本文综述了近年来电感耦合等离子体质谱在土壤样品分析测试中的应用,重点比较了土壤样品前处理中不同的消解体系和消解方式,介绍了激光熔蚀法、氢化物发生法和碰撞反应池技术等土壤环境监测中的新方法,以及ICP-MS在土壤环境监测中用于稀土元...     

润肤霜类化妆品中金属元素的测定及砷形态初探

采用电感耦合等离子体质谱(ICP-MS)测定化妆品中的金属元素铝、铬、镍、铜、锌、砷、硒、镉、锡、锑、钡、镧、铈、镨、钕、钐、汞、铅的总量,并结合液相色谱(HPLC)-ICPMS联用技术考察了化妆品中的砷形态.研究表明,金属指标不合格的化妆品多为汞含量超标;此外,化妆品中的砷多以无机砷形式存在.     

Inductively coupled plasma‐atomic emission spectroscopy in air and water pollution analysis†

The inductively coupled plasma (ICP), when employed as an excitation source in optical atomic emission spec.troscopy (AES), is finding widespread utilization for single and multielement inorganic trace analysis of pollutants. The recent availability of commercial ICP‐AES instrument systems has stimulated applications for the determination of metals and metalloids in diverse materials ranging from air particulates and fly ash to industrial effluents, sewage, and hard, soft, and saline waters.

The capabilities and limitations of ICP‐AES for applications in air and water pollution analysis are reviewed, and a number of recent examples presented.     

Online electro-Fenton-mass spectrometry reveals 2,4′,5-trichlorobiphenyl oxidation products and binding to organic matter

Electrochemistry–mass spectrometry is used to simulate redox reactions in many research disciplines because this technique is fast and provides information on compound metabolites. However, the analysis of the degradation of refractory organic pollutants by reactive oxygen species is difficult to achieve by the electrochemistry step. Therefore, here we use online electro-Fenton-mass spectrometry to study for the first time the oxidation of 2,4′,5-trichlorobiphenyl [polychlorinated biphenyl (PCB) 31] by reactive oxygen species and the binding reactions of PCB degradation products with model substances of natural organic matter. The degradation products were identified by coupled Q Trap mass spectrometry. We observed a binding of a degradation product with γ-l-glutamyl-l-cysteinyl-glycine. We propose a transformation pathway. We conclude that online electro-Fenton-mass spectrometry is a promising technique to study the oxidation of refractory organic pollutants and further binding of degradation products with natural organic matter.     

Air quality and PM10-associated poly-aromatic hydrocarbons around the railway traffic area: statistical and air mass trajectory approaches

Diesel engine railway traffic causes atmosphere pollution due to the exhaust emission which may be harmful to the passengers as well as workers. In this study, the air quality and PM₁₀ concentrations were evaluated around a railway station in Northeast India where trains are operated with diesel engines. The gaseous pollutant (e.g. SO₂, NO₂, and NH₃) was collected and measured by using ultraviolet–visible spectroscopy. The advanced level characterizations of the PM10 samples were carried out by using ion chromatography, Fourier-transform infrared, X-ray diffraction, inductively coupled plasma optical emission spectrometry , X-ray photoelectron spectroscopy, field-emission scanning electron microscopy with energy-dispersive spectroscopy, and high-resolution transmission electron microscopy with energy-dispersive spectroscopy techniques to know their possible environmental contaminants. High-performance liquid chromatography technique was used to determine the concentration of polycyclic aromatic hydrocarbons to estimate the possible atmospheric pollution level caused by the rail traffic in the enclosure. The average PM₁₀ concentration was found to be 262.11 µg m⁻³ (maximum 24 hour) which indicates poor air quality (AQI category) around the rail traffic. The statistical and air mass trajectory analysis was also done to know their mutual correlation and source apportionment. This study will modify traditional studies where only models are used to simulate the origins.

     

Organic and Inorganic Characterization of Marine Colloids

Isolates of the organic matter in the particulate, colloidal and dissolved states were obtained by tangential flow ultrafiltration through 0.40 μm polycarbonate and ∼ 1 nm (1000 NMWL*) regenerated cellulose membranes and by solid-liquid reverse phase extraction techniques. the material was analyzed qualitatively by mass spectroscopy, proton nuclear magnetic resonance, Fourier transform infrared spectroscopy, high performance liquid chromatography with fluorescence detection of labelled primary amines and amino acids, and inductively coupled plasma/mass spectroscopy. All three states are characterized by similar organic chemistries. the marine colloidal state in coastal waters off the Californian coast contains primarily carbohydrates, fatty acids, minor amounts of proteinaceous compounds and electropositive elements including aluminium and iron. Aromatic molecules and olefinic functional groups are in low concentration. the colloidal state differs qualitatively from the particulate and dissolved states. Yet all three could be derived, with degradation, from algal or macroalgal surface components.     

Organic and Inorganic Characterization of Marine Colloids

Abstract

Isolates of the organic matter in the particulate, colloidal and dissolved states were obtained by tangential flow ultrafiltration through 0.40 μm polycarbonate and ～ 1 nm (1000 NMWL?) regenerated cellulose membranes and by solid-liquid reverse phase extraction techniques. the material was analyzed qualitatively by mass spectroscopy, proton nuclear magnetic resonance, Fourier transform infrared spectroscopy, high performance liquid chromatography with fluorescence detection of labelled primary amines and amino acids, and inductively coupled plasma/mass spectroscopy. All three states are characterized by similar organic chemistries. the marine colloidal state in coastal waters off the Californian coast contains primarily carbohydrates, fatty acids, minor amounts of proteinaceous compounds and electropositive elements including aluminium and iron. Aromatic molecules and olefinic functional groups are in low concentration. the colloidal state differs qualitatively from the particulate and dissolved states. Yet all three could be derived, with degradation, from algal or macroalgal surface components.     

Research review trends of food analysis in Latvia: major and trace element content

The current paper involves overview of several studies concerning quantitative major and trace element analysis of different food samples, such as products of plant origin, e.g., locally grown vegetables (carrots, onions, potatoes) and products of animal origin derived with or without processing (cottage cheese, eggs, honey). Food samples were collected over the territory of Latvia in the time period 2009–2012. Sample pre-treatment was chosen according to the product specifics but mostly wet mineralization with concentrated nitric acid was applied. Analysis of major elements (e.g., Ca, Fe, K, Mg, Na) and trace elements (e.g., As, Cd, Co, Cr, Cu, Ni, Pb, Se, Zn) was performed by appropriate quantitative analytical technique: atomic absorption spectrometry, inductively coupled plasma mass spectrometry or total reflection X-ray fluorescence spectrometry. Not only the influence of environmental factors (e.g., geographical or seasonal impact) was detected in element dissemination in food, also botanical origin (if applicable) and applied agricultural praxis, product processing and storage specifics were found to be important. Possible food contamination by potentially toxic elements can be associated mostly with the consequences of anthropogenic activities. The studies revealed the significance of food research in the context of environmental science.     

Exposure to Selected Heavy Metals Through Water Ingestion in an Area Under the Influence of Tanneries

This study evaluated the potential toxicological risk posed to human health due to the exposure to heavy metals by water ingestion in an area affected by tanneries – the Cadeia-Feitoria hydrographic basin (Brazil). River water was collected at 10 sites, every 3 months, from July 1999 to April 2000. After acid digestion, total metal concentration was determined by inductively coupled plasma optical emission spectrometry (Cd, Cu, Cr, Ni, Zn), flame atomic absorption (Al, Fe, Pb, Mn), or cold vapor atomic absorption spectrometry (Hg). Cr(VI) was complexed with diphenyl-carbazide and detected by UV–vis spectrometry. In order to quantify the risk of exposure, the risk assessment methodology employed by the Environmental Protection Agency of the United States was applied at a screening level. The assumed scenarios included extreme exposure patterns (ingestion of untreated water, conversion of Cr(III) to Cr(VI), temporal peaks of pollution). Fe, Al, Cd, Hg, and Pb were not included in the risk analysis, since they showed a low toxicity potential or were undetected in the samples. The selected metals presented Hazard Quotients < 1, in the following order of increasing risk: Cu < Cr(III) < Zn < Ni < Mn < Cr(VI). Hazard indexes, representing the additive effect of contaminants, were also low in the basin (< 1), but comparatively increased in the lower reach of Feitoria and Cadeia Rivers. Although noncarcinogenic risk levels did not suggest possible adverse toxicological effects to the human population, a considerable deviation from background conditions was observed downstream the area where tanneries are mainly located.     

An evaluation of heavy metals contamination in soils from Ganzhou navel orange orchards by geoaccumulation indexes and statistical analysis

Heavy metal pollution in orchard soils is of increasing concern owing to the potential health risk via the food chain. The evaluations of the degree of heavy metal contamination and the potential sources in soils from navel orange orchards in the Ganzhou district were investigated in the present study with the geoaccumulation index and hierarchical cluster analysis. The soil samples were collected from 280 navel orange orchards located in the 18 counties of the Ganzhou district. The concentrations of heavy metals in the samples were determined using atomic fluorescence spectrometry and inductively coupled plasma atomic emission spectrometry with sample preparation by microwave digestion system. The results of the geoaccumulation index showed that the Ganzhou navel orange orchards were practically uncontaminated with Hg, As, Pb, Cd, Cr, Zn, and Cu, while uncontaminated to moderately contaminated with Ni. The results of cluster analysis indicated that four distinct clusters emerged for 18 sampling counties, and the considerable differences between clusters were derived from the different kinds of polluted substances. Results of the assessment of geoaccumulation index of heavy metals in soils will be helpful for the formulation of strategic sustainable agriculture in Ganzhou navel orchards and improvement of the navel orange yield and quality.     

Urinary stones as a novel matrix for human biomonitoring of toxic and essential elements

Monitoring of body burden of toxic elements is usually based on analysis of concentration of particular elements in blood, urine and/or hair. Analysis of these matrices, however, predominantly reflects short- or medium-term exposure to trace elements or pollutants. In this work, urinary stones were investigated as a matrix for monitoring long-term exposure to toxic and essential elements. A total of 431 samples of urinary calculi were subjected to mineralogical and elemental analysis by infrared spectroscopy and inductively coupled plasma mass spectrometry. The effect of mineralogical composition of the stones and other parameters such as sex, age and geographical location on contents of trace and minor elements is presented. Our results demonstrate the applicability of such approach and confirm that the analysis of urinary calculi can be helpful in providing complementary information on human exposure to trace metals and their excretion. Analysis of whewellite stones (calcium oxalate monohydrate) with content of phosphorus <0.6 % has been proved to be a promising tool for biomonitoring of trace and minor elements.

     

Automated indirect fluoride determination by ICP-OES using discontinuous-flow analysis

An automated method for the indirect determination of fluoride by inductively coupled plasma atomic emission spectrometry using discontinuous-flow analysis has been developed. A modified flow injection analysis system was used for sample preparation. The method is based on the determination of excess cerium(III) ion after precipitation of CeF₃. Separation of the precipitate is performed online on a syringe membrane filter that is cleaned each analysis cycle by 1 M nitric acid, ensuring a long life-time for the filter. As a result of the short reaction time, a detection limit of 9.5 mg L^?1 was obtained. The precision (RSD) of the proposed method is 1.02% at fluoride concentration of 28 mg L^?1. The applicability of the technique for groundwater monitoring of fluoride-contaminated area is demonstrated.     

The relationship between epilithic periphyton (biofilm) bound metals and metals bound to sediments in freshwater systems

Surficial sediments and epilithic periphyton (biofilm) were sampled from six sites on the River Churnet and five sites on the River Manifold in Staffordshire and analysed for cadmium (Cd), copper (Cu), lead (Pb) and zinc (Zn). The sites demonstrated a wide range of sediment trace metal concentrations determined by inductively coupled plasma optical emission spectrometry (ICP-OES) and atomic absorbtion spectroscopy (AAS). Biofilm was removed from the substrate using physical abrasion and 0.005 M ethylenediaminoethanetetra-acetic acid (EDTA) extractant. The European Standards, Measurements and Testing Programmes (BCR) operationally defined geochemical speciation scheme was used to determine the exchangeable, acid soluble fraction of the sediments. Significant positive correlations were determined between the EDTA extractable biofilm and the exchangeable sediment fraction for Cd, Cu and Zn but not for Pb. Natural epilithic periphyton may be a potential metal biomonitor particularly of Cu, Cd and Zn in aquatic systems and provide supporting information in relation to potential sediment toxicity.     

Concentrations of various elements and inorganic ions in rice straw and ash

Various elements and inorganic ions in rice straw and ash samples were analyzed by using inductively coupled plasma atomic emission spectrometry (ICP‐AES) and ion chromatography (IC). Five major elements: Mg, Mn, Al, Ca, and Fe and eight minor and trace elements: Cr, Cu, Ti, Zn, La, Sr, Ba, and Hg were detected in these samples, at more than ppm‐level. In ash samples the trace elements such as Y, As, V, Se, and Sc were also identified. The concentrations of SO₄, PO₄, Cl, Na, and K ions in these samples were higher than those of other ions measured. These elements and inorganic ion concentrations were approximately one order of magnitude higher in the ash than in the straw samples. Gas chromatography/mass spectrometry (GC/MS) and library search showed the presence of fatty‐, carboxylic‐ and nicotinic acids, and their derivatives in small quantities in the straw samples.     

Health risk of aerosols and toxic metals from incense and joss paper burning

We report for the first time the distribution and hazard potential of aerosol and metals resulting from joss paper burning. Burning joss paper and incense is a traditional custom in many Oriental countries. Large amounts of air pollutants, including particles, polycyclic aromatic hydrocarbons, toxic metals and other gaseous pollutants, are released into the environment during the burning stage. Many investigations have reported on the emission of pollutants from the incense burning. However, no work has been reported until now on the analysis of the released pollutants apart from polycyclic aromatic hydrocarbons. In this study, a micro-orifice uniform-deposit impactor and inductively coupled plasma optical emission spectrometry were, respectively, used to collect aerosols and characterize the toxic metals from joss paper burning. We studied two types of particulate matter (PM): PM_2.5 that are particles with a diameter smaller than 2.5 μm and PM₁₀ that are particles with a diameter smaller than 10 μm. PM_2.5 are the most potentially toxic particles. Our results showed that PM_2.5 are the major component of the pollutants and that the PM_2.5 to PM₁₀ ratio ranged from 62 to 99%. The metals Na, Ca, Mg, Al and K were the main species in the aerosol and in the bottom ash.