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Recent Developments in Trace Element Analysis by ICP-AES and ICP-MS with Particular Reference to Geological and Environmental Samples 总被引：1，自引：1，他引：1
Kathryn L. Linge 《Geostandards and Geoanalytical Research》2005,29(1):7-22
This review describes recent developments in trace element analysis using inductively coupled plasma-atomic emission spectrometry (ICP-AES) and inductively coupled plasma-mass spectrometry (ICP-MS). It aims to focus on the application of ICP techniques to geological and environmental samples. Therefore, fundamental studies in ICP-MS and ICP-AES instrumentation have largely been ignored. Whereas the majority of literature reviewed related to ICP-MS, indicating that ICP-MS is now the preferred technique for all geological analysis, there is still a steady development of ICP-AES to environmental applications. It is clear that true flexibility in elemental analysis can only be achieved by combining the advantages of both ICP-AES and ICP-MS. Two particular groups of elements (long-lived radionuclide and the platinum-group elements) stood out as warranting dedicated sections describing analytical developments these areas. 相似文献
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This review describes developments major and in trace element determination using atomic absorption spectroscopy (AAS), inductively coupled plasma-atomic emission spectrometry (ICP-AES), instrumental neutron activation analysis (INAA), and X-ray fluorescence (XRF) spectrometry that were reported in 2008 and 2009. Publication levels were comparable to those of previous years, except for XRF which showed an increase in the number of articles published in the past 2 years. In terms of number of publications and impact, the most active field was AAS, while INAA was the least active. As expected for well-established and mature methods, novel developments for all four analytical techniques were relatively sparse. For AAS, the most notable publications concerned developments in sample introduction, particularly focussing on solid samples, increasing analyte sensitivity, and higher sample throughput. For ICP-AES, publication of developments in sample introduction, remediation of matrix effects and calibration continues. Compared with past years, there was a clear focus on sample preconcentration methods, but very few publications reporting new hyphenated speciation methods. For INAA, there were several publications exploring the accuracy and robustness of the method, as well as the requirements for INAA to meet criteria for a primary method of measurement. Two other related techniques, delayed neutron activation analysis, and prompt gamma activation analysis, were also described. Hyphenated XRF techniques showed interesting developments in enabling XRF and XRD analysis on the same spot, and further work characterising and calibrating three-dimensional micro-XRF shows promising results for investigating sample heterogeneity. 相似文献
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Kathryn L. Linge 《Geostandards and Geoanalytical Research》2008,32(4):453-468
This review describes developments in trace element determination using inductively coupled plasma‐atomic emission spectrometry (ICP‐AES) and inductively coupled plasma‐mass spectrometry (ICP‐MS) that were reported in 2006 and 2007. It focuses on the application of ICP techniques to geological and environmental samples; fundamental studies in ICP‐MS and ICP‐AES instrumentation have largely been ignored. New advances in ICP‐MS and ICP‐AES were incremental over this period, partly because both techniques are now well‐established. A continuing shift towards the hyphenation of low‐flow separation techniques has sparked activity in the development of appropriate low‐flow interfaces, and papers discussing interference removal also contribute significantly to the volume of research for both ICP‐AES and ICP‐MS. Whereas the majority of new ICP publications concerned advances in ICP‐MS analysis rather than ICP‐AES, development for ICP‐AES still occurs in almost all areas, particularly in sample introduction and hyphenated techniques. 相似文献
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Jon D. Woodhead 《Geostandards and Geoanalytical Research》2005,29(1):26-36
This annual review documents developments and applications in the field of isotope ratio determination, as reflected in the literature for the Earth and environmental sciences for the year 2003. Particular emphasis is placed upon the relationship between the two dominant analytical techniques-thermal ionisation mass spectrometry (TIMS) and multi-collector inductively coupled plasma-mass spectrometry (MC-ICP-MS)-and the rapidly changing nature of their roles in isotope analysis. Additionally, the review covers developments in single-collector ICP-MS and TOF technologies, new sample preparation procedures and the characterisation of isotopic reference materials, together with fundamental investigations of mass spectrometer performance. 相似文献
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Chris RIDDLE Anthony VANDER VOET William DOHERTY 《Geostandards and Geoanalytical Research》1988,12(1):203-234
The applications of inductively coupled plasma -mass spectrometry (ICP-MS) to geoanalysis are reviewed. This technique offers the ability to determine elemental abundances and isotope ratios; it has proven to be sensitive, precise and accurate, and represents a significant advance in instrumentation suitable for rock analysis. This review deals principally with the application of ICP-MS to elemental analysis. Literature citations are complete as of December 31, 1987; particular attention has been paid to data reported for certified reference materials. Although most current ICP-MS analysis employs conventional nebulization of solution samples, there is considerable effort being made to develop viable alternative sample introduction schemes that can be applied to rock analysis. The lack of adequately defined certified reference rock materials is apparent for ICP-MS and other techniques that are capable of routine determinations in the ng/g (ppb) range. 相似文献
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《Journal of Geochemical Exploration》2005,86(2):104-118
Analyses by inductively coupled plasma atomic emission spectrometry (ICP-AES), inductively coupled plasma mass spectrometry (ICP-MS) and cold vapour atomic absorption (for Hg, CVAA) of a wide range of elements in some 300 surface water samples from the Salar de Uyuni and Salar de Coipasa catchments of the Bolivian Altiplano have been undertaken. Comparison of analyses of acidified aliquots of unfiltered sample water with water filtered at 0.45 μm reveals that the following elements are not affected significantly by filtration in this high-pH environment: B, Ca, Li, Mg, K, Si, Na, Sr, S. The following elements appear to experience significantly elevated concentrations in unfiltered samples, relative to filtered: Al, (As to a minor extent), Ba, Be, Cd, Cr, Co, Cu, Fe, Pb, Mn, Hg, Ni, P, Ag, Tl, Ti, V. The effect appears to be related to the presence, and subsequent dissolution in acid preservative, of Fe-, Al-or Mn-oxyhydroxide flocs (or coatings on silicate particles) in unfiltered samples, and their retention or precipitation on filters. 相似文献
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William J. Chazey III Clive R. Neal Jinesh C. Jain William S. Kinman 《Geostandards and Geoanalytical Research》2003,27(2):181-192
The geochemical reference material BHVO-1 was analysed by a variety of techniques over a six year period. These techniques included inductively coupled plasma-mass spectrometry and atomic emission spectroscopy (ICP-MS and ICP-AES, respectively), laser ablation ICP-MS and spark source mass spectroscopy. Inconsistencies between the published consensus values reported by Gladney and Roelandts (1988, Geostandards Newsletter) and the results of our study are noted for Rb, Y, Zr, Pb and Th. The values reported here for Rb, Y, Zr and Pb are generally lower, while Th is higher than the consensus value. This is not an analytical artefact unique to the University of Notre Dame ICP-MS facility, as most of the BHVO-1 analyses reported over the last ten to twenty years are in agreement with our results. We propose new consensus values for each of these elements as follows: Rb = 9.3 ± 0.2 μg g-1 (compared to 11 ± 2 μg g-1), Y = 24.4 ± 1.3 μg g-1 (compared to 27.6 ± 1.7 μg g-1), Zr = 172 ± 10 μg g-1 (compared to 179 ± 21 μg g-1), Pb = 2.2 ± 0.2 μg g-1 (compared to 2.6 ± 0.9 μg g-1) and Th = 1.22 ± 0.02 μg g-1 (compared to 1.08 ± 0.15 μg g-1). 相似文献
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Synthesis and Preliminary Characterisation of New Silicate, Phosphate and Titanite Reference Glasses 总被引：3，自引：0，他引：3
Stephan Klemme Stefan Prowatke Carsten Münker Charles W. Magee Yann Lahaye Thomas Zack Simone A. Kasemann E. Joan A. Cabato Benjamin Kaeser 《Geostandards and Geoanalytical Research》2008,32(1):39-54
Eleven synthetic silicate and phosphate glasses were prepared to serve as reference materials for in situ microanalysis of clinopyroxenes, apatite and titanite, and other phosphate and titanite phases. Analytical results using different micro-analytical techniques showed that the glass fragments were homogeneous in major and trace elements down to the micrometre scale. Trace element determinations using inductively coupled plasma-mass spectrometry (ICP-MS), multi-collector inductively coupled plasma-mass spectrometry (MC-ICP-MS), laser-ablation inductively coupled plasma-mass spectrometry (LA-ICP-MS) and secondary ionisation mass spectrometry (SIMS) showed good agreement for most elements (Li, Be, B, Cs, Rb, Ba, Sr, Ga, Pb, U, Th, Y, La, Ce, Pr, Nd, Sm, Eu, Gd, Er, Tm, Yb, Lu, Zr, Hf, Ta, Nb) studied and provide provisional recommended values. 相似文献
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Janet M. Hergt L. Paul Bédard Etienne Deloule Kathryn L. Linge Paul J. Sylvester Michael Wiedenbeck Jon D. Woodhead 《Geostandards and Geoanalytical Research》2005,29(1):5-52
The articles that comprise this critical review serve to draw attention to research papers published in specific fields of interest during 2003, provide critical comment on the relevance and importance of individual publications in these fields, and offer an overview of the comparative importance of advances in particular areas. In this way, these articles aim to assist experts in the field by keeping them informed of relevant recent publications, as well as providing an important resource for students or early career researchers who are embarking on studies in an area new to them. This year, five papers provide summaries of developments in bulk sample determinations employing (1) ICP-AES and ICP-MS (trace elements), (2) XRF and atomic absorption spectrometry and INAA, (3) isotope ratio measurements (TIMS, MC-ICP-MS, ICP-MS, ToF), as well as in situ measurements conducted using (4) secondary ion mass spectrometry and (5) laser ablation ICP-MS (trace element and isotope ratio determinations). 相似文献
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Parijat Roy Vysetti Balaram Anil Kumar Manavalan Satyanarayanan Thota Gnaneshwar Rao 《Geostandards and Geoanalytical Research》2007,31(3):261-273
Data on thirty-four minor and trace elements including all rare earth elements (REE) are reported for two kimberlitic international reference materials (SARM-39, MINTEK, RSA and MY-4, IGEM, Russia) by inductively coupled plasma-mass spectrometry (ICP-MS), some of them for the first time. Four digestion techniques (open acid, closed vessel acid, microwave and lithium metaborate fusion digestion) were used for the decomposition of samples for analysis by ICP-MS. Three other reference materials (USGS BHVO-1, CRPG BR-1 and ANRT UB-N) were analysed simultaneously using the same analytical methodology to assess the precision and accuracy of the determinations. The data obtained in this study compare well with working values wherever such values are available for comparison. Though open acid digestion was found to be very rapid, effective and convenient for the determination of several trace elements in kimberlitic samples, recoveries for heavy rare earth elements (HREE) were lower than the respective recoveries obtained by the other decomposition techniques used. The precision obtained was better than ± 6% RSD in the majority of cases with comparable accuracy. Chondrite-normalised plots of each RM for all the digestion techniques were smooth. The new data reported on the two kimberlitic reference materials make these samples useful for future geochemical studies of kimberlitic rocks. 相似文献