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《应用光谱学评论》2013,48(4):457-474
Abstract The literature concerning the improvement of atomic and ionic procedures for molybdenum determination through separation and pre‐concentration were updated. Analytical procedures based on flame atomic absorption spectrometry (AAAS), electrothermal or graphite furnace atomic absorption spectrometry (GFAAS), inductively coupled plasma optical emission spectrometry (ICP‐OES), and inductively coupled plasma mass spectrometry were reviewed taking into consideration the preliminary steps, which can enhance the selectivity and sensitivity based on co‐precipitation, solvent extraction, and solid‐phase extraction. Both in‐batch and on‐line procedures were considered. 相似文献
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Sergio Luis Costa Ferreira Manuel Miró Erik Galvão Paranhos da Silva Geraldo Domingues Matos Pedro Sanches dos Reis Geovani Cardoso Brandao 《应用光谱学评论》2013,48(1):44-62
Abstract This article critically overviews the state-of-the-art of slurry sampling as an approach for the minimization of sample preparation prior to the determination of metals and metalloids in complex matrices by spectroanalytical techniques. Relevant factors involved in the optimization of slurry-based analytical procedures and the dependence of the quality of the results on the calibration method selected are discussed in detail. The advantages and limitations compared to solid sampling for the analysis of solid matrices are highlighted and discussed. Analytical applications of slurry sampling reported in the literature emphasizing publications between 2004 and 2009 are comprehensively compiled covering detection by flame atomic absorption spectrometry (FAAS), electrothermal atomic absorption spectrometry (ET-AAS), cold vapor atomic absorption spectrometry (CV-AAS), hydride generation atomic absorption spectrometry (HG-AAS), hydride generation atomic fluorescence spectrometry (HG-AFS), inductively coupled plasma optical emission spectrometry (ICP-OES), and inductively coupled plasma mass spectrometry (ICP-MS). 相似文献
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《应用光谱学评论》2013,48(4):475-507
Abstract The application of metal (tantalum, molybdenum, and platinum) devices in analytical atomic spectrometry is reviewed in this article. These metal devices have been employed in various analytical atomic spectrometric techniques for more than three decades, mainly as electrothermal atomizers or electrothermal vaporizers, in various physical shapes, such as tubes, platforms, loops, and wires (or coils/filaments). Their application spans from atomic absorption spectrometry (AAS), atomic emission spectrometry (AES) atomic fluorescence spectrometry (AFS), inductively coupled plasma atomic emission spectrometry (ICP‐AES) to inductively coupled plasma mass spectrometry (ICP‐MS). The analytical figures of merit and the practical applications reported for these metal devices are reviewed, and the atomization mechanism on these metal atomizers is briefly summarized, too. In addition, other applications of the metal devices are discussed, including analyte preconcentration by electrodeposition and sequential metal vapor elution analysis (SMVEA). Furthermore, the application of these metals in graphite furnaces encompasses the schemes with the metals in the form of furnace linings, platforms, or impregnated salts. 相似文献
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Fábio G. Lepri Eduardo S. Chaves Mariana A. Vieira Anderson S. Ribeiro Adilson J. Curtius Lígia C. C. DeOliveira 《应用光谱学评论》2013,48(3):175-206
Abstract The determination of trace elements in edible oils and biodiesel using atomic spectrometric methods is reviewed. Problems related to sample pretreatment for appropriate sample introduction and calibration are addressed as well as the strategies to overcome them. Recent trends aimed at simplifying sample manipulation are presented. The applications and scope of atomic absorption spectrometry (AAS), flame optical emission spectrometry (F-OES), inductively coupled plasma–optical emission spectrometry (ICP-OES), and inductively coupled plasma–mass spectrometry (ICP-MS) techniques for the determination of trace metals in edible oils and biodiesel are discussed, as well as some current instrumental new developments. 相似文献
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S. L. C. Ferreira H. S. Ferreira G. D. Matos D. S. Anunciação W. N. L. dos Santos V. P. Campos 《应用光谱学评论》2013,48(8):633-653
Abstract: This article presents a critical evaluation of the analytical procedures used for the determination of lead in seawater, which is important because lead is a good indicator of marine pollution caused by human activities. Sampling, storage, and pretreatment techniques are briefly overviewed, including the significance of systematic errors that cannot be corrected later on. The main techniques in this article are electrothermal–atomic absorption spectrometry (ET-AAS), inductively coupled plasma–mass spectrometry (ICP-MS), and voltammetry. Flame atomic absorption spectrometry (FAAS) and inductively coupled plasma–optical emission spectrometry (ICP-OES) are treated as well, although their limits of quantification are not sufficient for a determination of lead in unpolluted seawater. Even when separation and preconcentration techniques are applied, these techniques are only capable of detecting lead in polluted coastal seawater. Separation and preconcentration are actually also required for ET-AAS and ICP-MS in order to determine the lowest concentrations of lead found in unpolluted open-ocean seawater, which is still a challenge for the analytical chemist. 相似文献
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Elo Harald Hansen 《应用光谱学评论》2013,48(4):335-357
Abstract One of the current needs within the analytical spectrometric community is the development of straightforward and cost‐effective, yet rugged, sample processing procedures aimed at precluding both spectroscopic and nonspectroscopic matrix interferences while fostering concomitant sample enrichment. Illustrated via selected representative examples, this review presents and discusses the current state of the art in implementing miniaturised and automated sample treatments for environmental and biochemical assays via microfluidic systems exploiting the lab‐on‐valve (LOV) platform in hyphenation with syringe pump propelling devices as a front end to a plethora of spectroscopic detection schemes including ultraviolet‐visible (UV‐Vis) spectrometry, spectrofluorimetry, chemiluminescence, atomic absorption spectrometry (AAS), atomic flourescence spectrometry (AFS), and inductively coupled plasma‐atomic emission spectrometry/mass spectrometry (ICP‐AES/MS). In contrast to lab‐on‐a‐chip units, the versatile configuration of the micromachined LOV readily facilitates the implementation of on‐line unit operations at will encompassing not merely the introduction of minute, well‐defined volumes of sample followed by chemical derivatization, but the potential for accommodation of solid‐phase extraction, hydride/vapor generation, precipitation/coprecipitation, and bead injection protocols with no need for chip redesign. 相似文献
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Abstract Internal standardization is a widely used method for compensating nonspectral interference in inductively coupled plasma (ICP) spectrometry. Emphasis is given on the choice of the suitable element and its specific spectral line as an efficient internal standard. This choice is the result of multi-variable evaluations and analytical applications. In inductively coupled plasma–atomic emission spectrometry (ICP-AES) and other spectrometric techniques several spectral lines of the same or different elements have been evaluated as potential internal standards. Yttrium spectral lines fulfill certain prerequisites and they are favored by a large number of researchers. In our discussed review, we present several reports of ICP-AES techniques that employ yttrium as the internal standard. These reports are classified according to specific sample origin and aim of the research. 相似文献
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Mirian C. Santos 《应用光谱学评论》2013,48(4):427-448
Abstract This review summarizes and discusses the preparation of slurries for analysis of inorganic materials by inductively coupled plasma optical emission spectrometry (ICP‐OES) and inductively coupled plasma mass spectrometry (ICP‐MS). Details about the grinding step for slurry preparation, the stabilization of slurries, and the calibration strategies are critically discussed. Typical applications described in the literature and the state‐of‐the‐art including advantages and limitations of slurry analysis are presented. 相似文献
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N. S. Mokgalaka 《应用光谱学评论》2013,48(2):131-150
Abstract The application of laser ablation inductively plasma mass spectrometry (LA‐ICP‐MS) to the determination of major, minor, and trace elements as well as isotope‐ratio measurements offers superior technology for direct solid sampling in analytical chemistry. The advantages of LA‐ICP‐MS include direct analysis of solids; no chemical dissolution is necessary, reduced risk of contamination, analysis of small sample mass, and determination of spatial distributions of elemental compositions. This review aims to summarize recent research to apply LA‐ICP‐MS, primarily in the field of environmental chemistry. Experimental systems, fractionation, calibration procedures, figures of merit, and new applications are discussed. Selected applications highlighting LA‐ICP‐MS are presented. 相似文献
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Abstract:This work presents an overview of the development of dry ashing preparation techniques for solid and quasisolid sample analysis by atomic and inorganic mass spectrometry, including flame/graphite furnace atomic absorption spectrometry, chemical vapor generation atomic absorption/fluorescence spectrometry, and inductively coupled plasma–optical emission/mass spectrometry. This article also summarizes all of the dry ashing methods reported in the past 20 years. The dry ashing methods applied to sample preparation are classified as electrothermal ashing, microwave ashing, oxygen combustion, and other special ashing methods including laser, ultraviolet (UV)/ozone, and plasma. Moreover, the development of relevant devices is discussed in context. 相似文献
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Abstract Even though normal exposure levels to Cd may be small, the human body is inefficient at excreting the heavy metal, so it slowly accumulates over the period of a lifetime. Eventually, the Cd level in the body may become toxic and give rise to harmful effects. Cadmium exposure could therefore be linked to diseases associated with aging such as osteoporosis, prostate cancer, and pancreatic cancer. These potential links have driven the development of a myriad of analytical techniques for the determination of Cd in biological samples. Natural biological Cd concentrations are typically low, so preconcentration steps and sensitive instruments are frequently a necessity. In addition, the complex matrices of biological specimens such as blood, urine, serum, and tissue often require a form of matrix modification or separation. This review provides an overview of these methods with 200 references from the literature published between 1995 and 2005. The analytical methods for the determination of Cd in biological samples include: spectrophotometry, atomic emission spectrometry, atomic absorption spectrometry, atomic fluorescence spectrometry, inductively coupled plasma mass spectrometry, and electrochemistry. In addition, Cd speciation techniques, using high‐performance liquid chromatography and capillary electrophoresis, are briefly discussed. 相似文献
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《应用光谱学评论》2013,48(1):71-99
Abstract High performance liquid chromatography (HPLC) has often been employed in the separation and speciation of metal containing compounds. One of the most sensitive devices used for detecting those compounds after the separation is the inductively coupled plasma (ICP). The similar flow rates for these two techniques render the coupling of the devices trivial, usually involving only a short length of capillary tubing. Upon entering the plasma, species are typically determined either via atomic emission spectrometry or mass spectrometry. HPLC-ICP devices have been employed less frequently for the determination of non-metals. This review will describe the applications of HPLC-ICP techniques to the determination of compounds containing carbon, sulfur, phosphorus, and the halogens. The instrumentation used for each application will be described, and the performance of the systems will be summarized. 相似文献
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Maria das Graças Andrade Korn Elane Santos da Boa Morte Daniele Cristina Muniz Batista dos Santos Jacira Teixeira Castro José Tiago Pereira Barbosa Alete Paixão Teixeira 《应用光谱学评论》2013,48(2):67-92
Abstract The present article gives an overview of recent publications and modern techniques of sample preparation for food analysis employing atomic and inorganic mass spectrometric techniques, such as flame atomic absorption spectrometry, chemical vapor generation atomic absorption and atomic fluorescence spectrometry, graphite furnace atomic absorption spectrometry, inductively coupled plasma optical emission spectrometry, and inductively coupled plasma mass spectrometry. Among the most frequently applied sample preparation techniques for food analysis are dry ashing, usually with the addition of an ashing aid, and acid digestion, preferably with the assistance of microwave energy. Slurry preparation, particularly with the assistance of ultrasound, is increasingly used to reduce acid consumption and sample preparation time. Direct analysis of solid samples is gaining importance in the field of food analysis as it offers the highest sensitivity, avoids the use of acids and other aggressive reagents, makes possible the analysis of micro‐samples, and can be applied for fast screening analysis, e.g., of fresh meat. 相似文献
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Rumyana Djingova Veronika Mihaylova Valentina Lyubomirova Dimiter L. Tsalev 《应用光谱学评论》2013,48(5):384-424
Abstract: The study of the ionome (ionomics) is defined as quantitative and simultaneous measurement of the element composition of living organisms and changes in this composition in response to physiological stimuli, development stage, and genetic modifications (Salt et al., Ann. Rev. Plant Biol., Vol. 59, 2008). The necessity of understanding the regulation processes of elements in the organisms demands determination of many elements in the organism, tissue, and cell (Baxter, Plant Biol., Vol. 12, 2009). A prospect for ionomics is environmental pollution where great variety of conditions and pollutants exist resulting in concentration and interelemental changes in the plant ionome. The capabilities of and problems with several multielement analytical techniques, including instrumental neutron activation analysis (INAA), X-ray fluorescence, inductively coupled plasma–atomic emission spectrometry (ICP-AES), inductively coupled plasma–mass spectrometry (ICP-MS), and atomic absorption spectrometry (AAS), which are adequate and most promising in ionomic and environmental studies of plants, are reviewed. References are confined mainly to the last 10–15 years. Information about concentrations, roles, binding forms, and pollution sources of the elements and comparison between methods with respect to limits of detection, determined elements, interferences, and economic considerations are tabulated. Some combinations of instrumental techniques supplementing each other are highly valued, namely, ICP-MS and ICP-AES and INAA and AAS or ICP-AES. 相似文献
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大气颗粒物重金属元素分析技术研究进展 总被引:3,自引:0,他引:3
大气颗粒物已经成为当前大气环境首要污染物,而其中重金属由于具有非降解性和滞后性,严重威胁人类生命和自然环境,已成为当前研究热点。对分析大气颗粒物中重金属元素所用原子吸收光谱法、电感耦合等离子体原子发射光谱法、电感耦合等离子体质谱法、荧光光谱法、中子活化法、辉光放电原子发射光谱法、微波等离子体原子发射光谱法和激光诱导击穿光谱法进行了综述,并尝试对这些技术的不足之处提出一些改进建议:连续光源原子吸收光谱法同时测定多种元素,原子发射光谱法直接测定颗粒物,高分辨率激光剥蚀电感耦合等离子质谱法测定固体样品,低散射同步加速荧光法测定大气颗粒物和k0中子活化法测定对流层发射性元素。大气颗粒物重金属元素的时空分布差异和人类对环境空气质量要求的提高以及现代仪器科学技术的高速发展促使大气颗粒物重金属元素分析技术朝着实时、快速、检出限低、直接测定和操作简便的方向发展。 相似文献
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Abstract The determination of Al, Cr, Cu, Fe, Mn, Mo, Ni, and Ti in digested stainless steel and nickel alloys using inductively coupled plasma atomic emission spectrometry with dual analytical lines was performed. Accuracy of the high solid solutions was assessed by comparison to standard values and found to be excellent. 相似文献