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Journal articles on the topic 'ICP-MS'

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Published: 4 June 2021
Last updated: 4 May 2024

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1

EMMETT, SUZANNE E. "ICP-MS." Alzheimer Disease & Associated Disorders 2, no. 3 (1988): 318. http://dx.doi.org/10.1097/00002093-198802030-00167.

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2

Vanhaecke, Frank. "ICP–MS." Analytical and Bioanalytical Chemistry 372, no. 1 (December 8, 2001): 20–21. http://dx.doi.org/10.1007/s00216-001-1147-0.

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3

Mitrano, Denise M., Angela Barber, Anthony Bednar, Paul Westerhoff, Christopher P. Higgins, and James F. Ranville. "Silver nanoparticle characterization using single particle ICP-MS (SP-ICP-MS) and asymmetrical flow field flow fractionation ICP-MS (AF4-ICP-MS)." Journal of Analytical Atomic Spectrometry 27, no. 7 (2012): 1131. http://dx.doi.org/10.1039/c2ja30021d.

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4

Gallo, Jenny M., and Jose R. Almirall. "Elemental analysis of white cotton fiber evidence using solution ICP-MS and laser ablation ICP-MS (LA-ICP-MS)." Forensic Science International 190, no. 1-3 (September 2009): 52–57. http://dx.doi.org/10.1016/j.forsciint.2009.05.011.

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5

KUROKI, Yasuo. "Laser Ablation-ICP-MS." Journal of The Surface Finishing Society of Japan 72, no. 3 (March 1, 2021): 145–49. http://dx.doi.org/10.4139/sfj.72.145.

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6

Krupp, Eva. "Kopplungstechniken mit ICP-MS." Nachrichten aus der Chemie 56, no. 5 (May 2008): 555–59. http://dx.doi.org/10.1002/nadc.200853351.

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7

Olesik, John W. "Elemental Analysis Using ICP-OES and ICP/MS." Analytical Chemistry 63, no. 1 (January 1991): 12A—21A. http://dx.doi.org/10.1021/ac00001a711.

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8

Yang, He S., Delecia R. LaFrance, and Ying Hao. "Elemental Testing Using Inductively Coupled Plasma Mass Spectrometry in Clinical Laboratories." American Journal of Clinical Pathology 156, no. 2 (May 12, 2021): 167–75. http://dx.doi.org/10.1093/ajcp/aqab013.

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Abstract Objectives This review aims to describe the principles underlying different types of inductively coupled plasma mass spectrometry (ICP-MS), and major technical advancements that reduce spectral interferences, as well as their suitability and wide applications in clinical laboratories. Methods A literature survey was performed to review the technical aspects of ICP-MS, ICP-MS/MS, high-resolution ICP-MS, and their applications in disease diagnosis and monitoring. Results Compared to the atomic absorption spectrometry and ICP-optical emission spectrometry, ICP-MS has advantages including improved precision, sensitivity and accuracy, wide linear dynamic range, multielement measurement capability, and ability to perform isotopic analysis. Technical advancements, such as collision/reaction cells, triple quadrupole ICP-MS, and sector-field ICP-MS, have been introduced to improve resolving power and reduce interferences. Cases are discussed that highlight the clinical applications of ICP-MS including determination of toxic elements, quantification of nutritional elements, monitoring elemental deficiency in metabolic disease, and multielement analysis. Conclusions This review provides insight on the strategies of elemental analysis in clinical laboratories and demonstrates current and emerging clinical applications of ICP-MS.
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9

Holmes, L. "Determination of Thorium by ICP-MS and ICP-OES." Radiation Protection Dosimetry 97, no. 2 (October 1, 2001): 117–22. http://dx.doi.org/10.1093/oxfordjournals.rpd.a006647.

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10

YAMASAKI, Shin-ichi. "Soil analyses by ICP-MS." BUNSEKI KAGAKU 49, no. 4 (2000): 217–24. http://dx.doi.org/10.2116/bunsekikagaku.49.217.

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11

Russo, Richard E., Xianglei Mao, Jhanis J. Gonzalez, and Samuel S. Mao. "Femtosecond laser ablation ICP-MS." J. Anal. At. Spectrom. 17, no. 9 (2002): 1072–75. http://dx.doi.org/10.1039/b202044k.

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12

Labat, Laurence, Christine Dhorne, Florian Klinzig, Betty Dehon, and Michel Lhermitte. "ICP-MS et toxicologie professionnelle." Annales de Toxicologie Analytique 19, no. 1 (2007): 23–29. http://dx.doi.org/10.1051/ata:2007004.

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13

Venth, K., K. Danzer, G. Kundermann, and K. H. Blaufu�. "Multisignal evaluation in ICP-MS." Analytical and Bioanalytical Chemistry 354, no. 7-8 (March 1, 1996): 811–17. http://dx.doi.org/10.1007/s0021663540811.

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14

Bustos, Antonio R. Montoro, and Michael R. Winchester. "Single-particle-ICP-MS advances." Analytical and Bioanalytical Chemistry 408, no. 19 (May 21, 2016): 5051–52. http://dx.doi.org/10.1007/s00216-016-9638-1.

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15

Wennrich, Rainer, Karsten Grüke, and Annette Walther. "Umweltanalytik mit ETV-ICP-MS." Nachrichten aus Chemie, Technik und Laboratorium 45, no. 3 (March 1997): 291–95. http://dx.doi.org/10.1002/nadc.19970450315.

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16

Begerow, Jutta, and Lothar Dunemann. "ICP-MS bei biologischen Proben." Nachrichten aus Chemie, Technik und Laboratorium 44, no. 7-8 (July 1996): 739–43. http://dx.doi.org/10.1002/nadc.19960440717.

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17

Paul, Michael, and Shona McSheehy. "Elementspezies bestimmen mit ICP-MS." Nachrichten aus der Chemie 55, no. 7-8 (July 2007): 766–69. http://dx.doi.org/10.1002/nadc.200744615.

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18

Choi, Sung Hwa, Jae Sung Kim, Ji Yeon Lee, Ji Suk Jeon, Ju Wan Kim, Richard E. Russo, Jhanis Gonzalez, et al. "Analysis of arsenic in rice grains using ICP-MS and fs LA-ICP-MS." J. Anal. At. Spectrom. 29, no. 7 (2014): 1233–37. http://dx.doi.org/10.1039/c4ja00069b.

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With rice being the main staple crop in Asian countries such as China, Korea and Japan, the detection of arsenic (As), an element known to be carcinogenic to humans, has been the topic of high public interest.
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19

Nikolaeva, I. V., A. A. Kravchenko, S. V. Palessky, S. V. Nechepurenko, and D. V. Semenova. "ICP-MS AND ICP-AES ANALYSIS OF PLANT REFERENCE MATERIALS." Industrial laboratory. Diagnostics of materials 85, no. 6 (July 10, 2019): 11–24. http://dx.doi.org/10.26896/1028-6861-2019-85-6-11-24.

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Two methods — ICP-MS and ICP-AES are used for certification of the new reference material — needles of Siberian pine (NSP-1). Techniques of the analysis include decomposition of plant samples in two different ways: acid digestion in a microwave system MARS-5 and lithium metaborate fusion followed by ICP-MS and ICP-AES analysis of the solutions. Simultaneous determinations of all the elements were carried out in low, medium and high resolution using SF-mass-spectrometer ELEMENT and atomic-emission spectrometer IRIS Advantage with external calibrations and internal standards (In — ICP-MS, Sc —ICP-AES). Middle and high resolutions of ICP mass spectrometer were used for interference corrections. Data obtained by ICP-MS and ICP-AES with different decomposition techniques are in good agreement. The ICP-MS and ICP-AES techniques have been validated by the analysis of three plant reference materials: LB-1 (leaf of a birch), Tr-1 (grass mixture) and EK-1 (Canadian pondweed). These techniques were used for the determination of 38 elements in the new reference material NSP-1. Relative standard deviations for most of the determined elements were below 10%. Combination of ICP-MS and ICP-AES techniques for certification of the new reference material makes it possible to expand the set of elements to be determined and to reduce the total analysis time.
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20

Meng, Ziwei, Lingna Zheng, Hao Fang, Pu Yang, Bing Wang, Liang Li, Meng Wang, and Weiyue Feng. "Single Particle Inductively Coupled Plasma Time-of-Flight Mass Spectrometry—A Powerful Tool for the Analysis of Nanoparticles in the Environment." Processes 11, no. 4 (April 17, 2023): 1237. http://dx.doi.org/10.3390/pr11041237.

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Single-particle inductively coupled plasma-mass spectrometry (SP-ICP-MS) has emerged as an important tool for the characterization of inorganic nanoparticles (NPs) in the environment. Although most SP-ICP-MS applications rely on the quadrupole ICP-MS (ICP-QMS), it is limited by the slow scanning speed of the quadrupole. Recent advancements in instrumentation have led to the development of inductively coupled plasma time-of-flight mass spectrometry (ICP-TOF-MS) which offers a viable solution. In this review, we discuss the recent advances in instrumentation and methodology of ICP-TOF-MS, followed by a detailed discussion of the applications of SP-ICP-TOFMS in analyzing NPs in the environment. SP-ICP-TOFMS has the potential to identify and quantify both anthropogenic and natural NPs in the environment, providing valuable insights into their occurrence, fate, behavior, and potential environmental risks.
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21

Faßbender, Sebastian, Marcus von der Au, Maren Koenig, Jürgen Pelzer, Christian Piechotta, Jochen Vogl, and Björn Meermann. "Species-specific isotope dilution analysis of monomethylmercury in sediment using GC/ICP-ToF-MS and comparison with ICP-Q-MS and ICP-SF-MS." Analytical and Bioanalytical Chemistry 413, no. 21 (July 23, 2021): 5279–89. http://dx.doi.org/10.1007/s00216-021-03497-z.

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AbstractA recently introduced inductively coupled plasma-time-of-flight-mass spectrometer (ICP-ToF-MS) shows enhanced sensitivity compared to previous developments and superior isotope ratio precision compared to other ToF and commonly used single-collector ICP-MS instruments. Following this fact, an improvement for isotope dilution ICP-MS using the new instrumentation has been reported. This study aimed at investigating whether this improvement also meets the requirements of species-specific isotope dilution using GC/ICP-MS, where short transient signals are recorded. The results of the analysis of monomethylmercury (MMHg) of a sediment reference material show that isotope ratio precision of ICP-MS instruments equipped with quadrupole, sector-field, and time-of-flight mass analyzers is similar within a broad range of peak signal-to-noise ratio when analyzing one isotopic system. The procedural limit of quantification (LOQ) for MMHg, expressed as mass fraction of Hg being present as MMHg, w(Hg)MMHg, was similar as well for all investigated instruments and ranged between 0.003 and 0.016 μg/kg. Due to the simultaneous detection capability, the ICP-ToF-MS might, however, be more favorable when several isotopic systems are analyzed within one measurement. In a case study, the GC/ICP-ToF-MS coupling was applied for analysis of MMHg in sediments of Finow Canal, a historic German canal heavily polluted with mercury. Mass fractions between 0.180 and 41 μg/kg (w(Hg)MMHg) for MMHg, and 0.056 and 126 mg/kg (w(Hg)total) for total mercury were found in sediment samples taken from the canal upstream and downstream of a former chemical plant. Graphical abstract
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22

Hanousek, Ondrej, Marion Brunner, Daniel Pröfrock, Johanna Irrgeher, and Thomas Prohaska. "The performance of single and multi-collector ICP-MS instruments for fast and reliable34S/32S isotope ratio measurements." Analytical Methods 8, no. 42 (2016): 7661–72. http://dx.doi.org/10.1039/c6ay02177h.

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The performance and validation characteristics of different single collector inductively coupled plasma mass spectrometers based on different technical principles (ICP-SFMS, ICP-QMS in reaction and collision modes, and ICP-MS/MS) were evaluated in comparison to the performance of MC ICP-MS for fast and reliable S isotope ratio measurements.
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23

Schudel, Gary, Vivian Lai, Kathy Gordon, and Dominique Weis. "Trace element characterization of USGS reference materials by HR-ICP-MS and Q-ICP-MS." Chemical Geology 410 (September 2015): 223–36. http://dx.doi.org/10.1016/j.chemgeo.2015.06.006.

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24

Kirby, Jason, William Maher, Michael Ellwood, and Frank Krikowa. "Arsenic Species Determination in Biological Tissues by HPLC - ICP - MS and HPLC - HG - ICP - MS." Australian Journal of Chemistry 57, no. 10 (2004): 957. http://dx.doi.org/10.1071/ch04094.

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The use of high-pressure liquid chromatography coupled directly or by a hydride generation system to an inductively coupled plasma mass spectrometer for the unambiguous measurement of 13 arsenic species in marine biological extracts is described. The use of two chromatography systems; a Supelcosil LC-SCX cation-exchange column eluted with a 20 mM pyridine mobile phase adjusted to pH 2.2 and 2.6 with formic acid, with a flow rate of 1.5 mL min−1 at 40°C, and a Hamilton PRP-X100 anion-exchange column eluted with 20 mM NH4H2PO4 buffer at pH 5.6, with a flow rate of 1.5 mL min−1 at 40°C, was required to separate and quantify cation and anion arsenic species. Under these conditions, arsenous acid could not be separated from other arsenic species and required the use of an additional hydride generation step. Arsenic species concentrations in a locally available Tasmanian kelp (Durvillea potatorum), a certified reference material (DORM-2), and a range of commercially available macroalgae supplements and sushi seaweeds have been measured and are provided for use as in-house quality control samples to assess the effectiveness of sample preparation, extraction, and measurement techniques.
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25

FUJIMORI, Eiji, and Hiroki HARAGUCHI. "Plasma and Emission Spectrometry II. ICP-AES and ICP-MS." Journal of the Spectroscopical Society of Japan 56, no. 2 (2007): 74–85. http://dx.doi.org/10.5111/bunkou.56.74.

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26

Al-Rashdan, A., D. Heitkemper, and J. A. Caruso. "Lead Speciation by HPLC--ICP--AES and HPLC--ICP--MS." Journal of Chromatographic Science 29, no. 3 (March 1, 1991): 98–102. http://dx.doi.org/10.1093/chromsci/29.3.98.

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27

Vrijens, Jan, Pedro Couck, Carmen Schroijen, Willy Baeyens, and Martine Leermakers. "Spectral interferences in the analysis of cadmium in human blood by ICP-MS: comparison between high resolution sector field ICP-MS and quadrupole ICP-MS." Journal of Analytical Atomic Spectrometry 26, no. 9 (2011): 1819. http://dx.doi.org/10.1039/c1ja10085h.

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28

Yang, Guosheng, Jian Zheng, Eunjoo Kim, Shuai Zhang, Hatsuho Seno, Munehiko Kowatari, Tatsuo Aono, and Osamu Kurihara. "Rapid analysis of 237Np and Pu isotopes in small volume urine by SF-ICP-MS and ICP-MS/MS." Analytica Chimica Acta 1158 (May 2021): 338431. http://dx.doi.org/10.1016/j.aca.2021.338431.

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29

Goda, Motoki, and Yohichiro Kojima. "Possible classification of pork products by ICP-MS." Journal of the Institute of Industrial Applications Engineers 8, no. 2 (April 25, 2020): 46–49. http://dx.doi.org/10.12792/jiiae.8.46.

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30

Balaram, V. "Inductively Coupled Plasma-Tandem Mass Spectrometry (ICP-MS/MS) and Its Applications." Journal of ISAS 1, no. 1 (July 31, 2022): 1–26. http://dx.doi.org/10.59143/isas.jisas.1.1.cnyr8764.

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During the last about 10 years, the inductively coupled plasma tandem quadrupole mass spectrometry (ICP-MS/MS) technique with reaction cell is being utilized for the analyses of several trace elements/isotopes at very low concentration levels in a variety of matrices including geological, environmental, biological, medical, nuclear, agriculture, food, material and metallurgical sciences. Both solution nebulization, as well as direct analysis of samples by laser ablation (LA-ICP-MS/MS), are utilized for sample introduction. In fact, ICP-MS/MS technique with collision reaction cells eliminated the need for laborious chemical separations using methods such as ion-exchange or solvent extraction procedures to eliminate/minimize spectral and matrix interference effects as these interferences are removed using online chemical reactions within the instrument itself (chemical resolution). In addition, the technique is hyphenated with chromatographic techniques such as GC and HPLCfor a variety of applications. The detection limits for several elements in the periodic table lie in the pg/ml-fg/ml range, and the technique compares favourably with the expensive, complex, and superior high resolution-ICP-MS (HR-ICP-MS), both in terms of the detection limits as well as the ability to remove the most complex interferences. Thus, the ICP MS/MS made the determinations of elemental as well as isotopic concentrations very simple andeasy even in complex materials with several novel quantification approaches. This article provides an overview of these new developments during the last decade along with several applications in all areas of science and technology.
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31

Balaram, V. "Inductively Coupled Plasma-Tandem Mass Spectrometry (ICP-MS/MS) and Its Applications." Journal of ISAS 1, no. 1 (July 31, 2022): 1–26. http://dx.doi.org/10.59143/isas.jisas.1.1.lhbp9335.

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During the last about 10 years, the inductively coupled plasma tandem quadrupole mass spectrometry (ICP-MS/MS) technique with reaction cell is being utilized for the analyses of several trace elements/isotopes at very low concentration levels in a variety of matrices including geological, environmental, biological, medical, nuclear, agriculture, food, material and metallurgical sciences. Both solution nebulization, as well as direct analysis of samples by laser ablation (LA-ICP-MS/MS), are utilized for sample introduction. In fact, ICP-MS/MS technique with collision reaction cells eliminated the need for laborious chemical separations using methods such as ion-exchange or solvent extraction procedures to eliminate/minimize spectral and matrix interference effects as these interferences are removed using online chemical reactions within the instrument itself (chemical resolution). In addition, the technique is hyphenated with chromatographic techniques such as GC and HPLCfor a variety of applications. The detection limits for several elements in the periodic table lie in the pg/ml-fg/ml range, and the technique compares favourably with the expensive, complex, and superior high resolution-ICP-MS (HR-ICP-MS), both in terms of the detection limits as well as the ability to remove the most complex interferences. Thus, the ICP MS/MS made the determinations of elemental as well as isotopic concentrations very simple andeasy even in complex materials with several novel quantification approaches. This article provides an overview of these new developments during the last decade along with several applications in all areas of science and technology.
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32

Thompson, Jay M., Leonid V. Danyushevsky, Olga Borovinskaya, and Martin Tanner. "Time-of-flight ICP-MS laser ablation zircon geochronology: assessment and comparison against quadrupole ICP-MS." Journal of Analytical Atomic Spectrometry 35, no. 10 (2020): 2282–97. http://dx.doi.org/10.1039/d0ja00252f.

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This study presents U–Pb isotopic and trace element results from the mineral zircon measured by nanosecond laser ablation coupled to either a time-of-flight ICP-MS, a quadrupole ICP-MS or both via a split stream arrangement.
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33

Frei, Dirk, Julie A. Hollis, Axel Gerdes, Dan Harlov, Christine Karlsson, Paulina Vasquez, Gerhard Franz, Leif Johansson, and Christian Knudsen. "Advanced in situ geochronological and trace element microanalysis by laser ablation techniques." Geological Survey of Denmark and Greenland (GEUS) Bulletin 10 (November 29, 2006): 25–28. http://dx.doi.org/10.34194/geusb.v10.4884.

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Laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) was developed in 1985 and the first commercial laser ablation systems were introduced in the mid 1990s. Since then, LA-ICP-MS has become an important analytical tool in the earth sciences. Initially, the main interest for geologists was in its ability to quantitatively determine the contents of a wide range of elements in many minerals at very low concentrations (a few ppm and below) with relatively high spatial resolution (spot diameters of typically 30–100 μm). The potential of LA-ICP-MS for rapid in situ U–Th–Pb geochronology was already realised in the early to mid 1990s. However, the full potential of LA-ICP-MS as the low-cost alternative to ion-microprobe techniques for highly precise and accurate in situ U–Th–Pb age dating was not realised until the relatively recent advances in laser technologies and the introduction of magnetic sectorfield ICP-MS (SF-ICPMS) instruments. In March 2005, the Geological Survey of Denmark and Greenland (GEUS) commissioned a new laser ablation magnetic sectorfield inductively coupled plasma mass spectrometry (LA-SF-ICP-MS) facility employing a ThermoFinnigan Element2 high resolution magnetic sectorfield ICP-MS and a Merchantek New Wave 213 nm UV laser ablation system. The new GEUS LA-SF-ICP-MS facility is widely used on Survey research projects in Denmark and Greenland, as well as in collaborative research and contract projects conducted with partners from academia and industry worldwide. Here, we present examples from some of the these ongoing studies that highlight the application of the new facility for advanced geochronological and trace element in situ microanalysis of geomaterials. The application of LASF-ICP-MS based in situ zircon geochronology to regional studies addressing the Archaean geology of southern West Greenland is presented by Hollis et al. (2006, this volume).
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34

Narukawa, T., T. Iwai, and K. Chiba. "An ICP index for ICP-MS determinations – new selection rules for internal standards in ICP-MS determinations and carbon enhancement effect." Journal of Analytical Atomic Spectrometry 32, no. 8 (2017): 1547–53. http://dx.doi.org/10.1039/c7ja00132k.

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35

Gäbler, Hans-Eike, Sönke Rehder, Andreas Bahr, Frank Melcher, and Simon Goldmann. "Cassiterite fingerprinting by LA-ICP-MS." Journal of Analytical Atomic Spectrometry 28, no. 8 (2013): 1247. http://dx.doi.org/10.1039/c3ja50106j.

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36

Yakimovich, P. V., and A. V. Alekseev. "Analysis of Wastewater by ICP-MS." Metallurgist 62, no. 1-2 (May 2018): 3–9. http://dx.doi.org/10.1007/s11015-018-0617-y.

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37

Zoorob, Grace K., John W. McKiernan, and Joseph A. Caruso. "ICP-MS for elemental speciation studies." Mikrochimica Acta 128, no. 3-4 (September 1998): 145–68. http://dx.doi.org/10.1007/bf01243044.

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38

Kuß, Heinz-Martin. "Spurenelementanalytik von Stählen mit ICP-MS." Nachrichten aus Chemie, Technik und Laboratorium 43, no. 7-8 (July 1995): 804–8. http://dx.doi.org/10.1002/nadc.19950430717.

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39

Huynh, Thi-Ngoc Suong, Claude Vidaud, and Agnès Hagège. "Investigation of uranium interactions with calcium phosphate-binding proteins using ICP/MS and CE-ICP/MS." Metallomics 8, no. 11 (2016): 1185–92. http://dx.doi.org/10.1039/c6mt00147e.

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40

Grottoli, Andréa G., Kathryn A. Matthews, James E. Palardy, and William F. McDonough. "High resolution coral Cd measurements using LA-ICP-MS and ID-ICP-MS: Calibration and interpretation." Chemical Geology 356 (October 2013): 151–59. http://dx.doi.org/10.1016/j.chemgeo.2013.08.024.

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41

Gschwind, Sabrina, Maria de Lourdes Aja Montes, and Detlef Günther. "Comparison of sp-ICP-MS and MDG-ICP-MS for the determination of particle number concentration." Analytical and Bioanalytical Chemistry 407, no. 14 (March 22, 2015): 4035–44. http://dx.doi.org/10.1007/s00216-015-8620-7.

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42

Brown, R., D. J. Gray, and D. Tye. "Hydride generation ICP-MS (HG-ICP-MS) for the ultra lowlevel determination of mercury in biota." Water, Air, & Soil Pollution 80, no. 1-4 (February 1995): 1237–45. http://dx.doi.org/10.1007/bf01189787.

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43

Becker, J. Sabine, M. Zoriy, Valderi L. Dressler, Bei Wu, and J. Susanne Becker. "Imaging of metals and metal-containing species in biological tissues and on gels by laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS): A new analytical strategy for applications in life sciences." Pure and Applied Chemistry 80, no. 12 (January 1, 2008): 2643–55. http://dx.doi.org/10.1351/pac200880122643.

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Laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) has become established as a very efficient and sensitive trace, ultratrace, and surface analytical technique in the life sciences. We have developed a new analytical imaging technique using LA-ICP-MS to study element distribution in biological tissues. Nowadays, LA imaging ICP-MS using double-focusing sector field (LA-ICP-SFMS) or quadrupole-based mass spectrometers (LA-ICP-QMS) can be applied as an exciting tool providing new information on the pathophysiology, pharmacology, and toxicology of elements of interest in biological systems. The quantitative determination of elements (e.g., Cu, Fe, Zn, Se, and others) in biological tissues is of growing interest especially in brain research (e.g., for studying neurodegenerative diseases such as Alzheimer's or Parkinson's disease). LA-ICP-SFMS was employed to produce images of detailed regionally specific element distributions in thin tissue sections of different sizes (such as control human or rat brain tissues or tumor regions). In addition, imaging MS using LA-ICP-QMS was applied to study the uptake and transport of nutrient and toxic elements in plant tissues.Besides the quantitative imaging of essential and toxic elements in tissues, powerful analytical techniques are also required for the determination and characterization of phosphoproteins and metal-containing proteins within a large pool of proteins, after electrophoretic separation (e.g., blue native, BN and sodium dodecyl sulfate-polyacrylamide gel electrophoresis, SDS-PAGE) into 1D and 2D gels. LA-ICP-MS was used to detect metalloproteins in protein bands of 1D gels or protein spots separated after 2D gel electrophoresis (2D-GE). In addition to elemental determination by LA-ICP-MS, matrix-assisted laser desorption/ionization (MALDI)-MS was employed to identify metal-containing proteins. Recent progress will be discussed in applying LA-ICP-MS in the life sciences, including the imaging of thin slices of tissue and applications in proteome analysis in combination with MALDI-MS to investigate phosphoproteins and metal-containing proteins.
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44

Popov, Daniil V. "Short communication: On the potential use of materials with heterogeneously distributed parent and daughter isotopes as primary standards for non-U–Pb geochronological applications of laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS)." Geochronology 4, no. 1 (June 15, 2022): 399–407. http://dx.doi.org/10.5194/gchron-4-399-2022.

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Abstract. Many new geochronological applications of laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) have been proposed in recent years. One of the problems associated with this rapid growth is the lack of chemically and isotopically homogeneous matrix-matched primary standards to control elemental fractionation during LA-ICP-MS analysis. In U–Pb geochronological applications of LA-ICP-MS this problem is often addressed by utilising matrix-matched primary standards with variable chemical and isotopic compositions. Here I derive a set of equations to adopt this approach for non-U–Pb geochronological applications of LA-ICP-MS.
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45

Jia, Xiujuan, Tiebang Wang, Xiaodong Bu, Qiang Tu, Sandra Spencer, Xiaoyi Gong, and Theresa Natishan. "Study of hypochlorite-specific enhancement in ICP-AES and ICP-MS." Journal of Analytical Atomic Spectrometry 20, no. 11 (2005): 1293. http://dx.doi.org/10.1039/b504846j.

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46

Pécheyran, C. "ICP-AES and ICP-MS: Trends at Pittcon'98 (in French)." Analusis 26, no. 4 (May 1998): 88–90. http://dx.doi.org/10.1051/analusis:199826040088.

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47

Valentin, Jenna L., and R. John Watling. "Provenance establishment of coffee using solution ICP-MS and ICP-AES." Food Chemistry 141, no. 1 (November 2013): 98–104. http://dx.doi.org/10.1016/j.foodchem.2013.02.101.

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48

Ding, Lihua, Guang Yang, Fang Xia, Claire E. Lenehan, Gujie Qian, Aoife McFadden, Joël Brugger, Xianghua Zhang, Guorong Chen, and Allan Pring. "A LA-ICP-MS sulphide calibration standard based on a chalcogenide glass." Mineralogical Magazine 75, no. 2 (April 2011): 279–87. http://dx.doi.org/10.1180/minmag.2011.075.2.279.

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AbstractThe accurate measurement of trace element concentrations in natural sulphides by laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) has been limited by the lack of matrix-matched calibration standards. The synthesis of a standard, IMER-1, by incorporating four minor and 34 trace elements into a chalcogenide glass matrix Ge28Sb12S60is reported here. Chemical analysis by electron probe microanalysis (EPMA), LA-ICP-MS, solution ICP-MS, and inductively coupled plasma-optical emission spectroscopy (ICP-OES) confirmed the excellent homogeneity of major elements (1-σ relative standard deviation (RSD) <1% for S, Sb and Ge) and acceptable homogeneity of most trace elements (1-σ RSD <10%). The standard was validated by analysing trace-elements concentrations in three geological pyrite specimens using IMER-1 as the calibration standard and comparing the results to previously reported values also determined by LA-ICP-MS but using a different calibration standard. STDGL2b-2. The results suggest that IMER-1 may be an appropriate calibration standard for LA-ICP-MS analysis of trace elements in natural sulphides.
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49

Bilqis, Nabilah, Erni Sulistiawati, and Miftakh Nur Rahman. "Application of The Inductively Coupled Plasma-Mass Spectrometry (ICP-MS) Method in Zinc Analysis." JURNAL SAINS NATURAL 12, no. 1 (January 27, 2022): 23. http://dx.doi.org/10.31938/jsn.v12i1.321.

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Zinc is a nutrient that affects cell growth, helps the body's metabolism, activates T cells (T lymphocytes), cell regeneration, and repairs body tissues. Zinc in the body undergoes a process of excretion every day, therefore daily intake of zinc needs to be considered to maintain the amount of zinc in the body in a normal amount. This study aimed to obtain information on the application of the Inductively coupled plasma-mass spectrometry (ICP-MS) method to determine the concentration of zinc in the serum of pregnant women. The application of Inductively coupled plasma-mass spectrometry (ICP-MS) method in zinc analysis provided the advantages of a minimal sample volume requirement with higher instrument sensitivity, fast retention time and had a concentration detection limit of up to parts per billion (ppb). Analysis of the zinc concentration in the serum of pregnant women using the ICP-MS method showed 80% serum with a concentration below the reference value, 13.3% normal and 6.7% a concentration higher than the WHO reference value.Keywords: defisiensi zink, inductively coupled plasma-mass spectrometry (icp-ms), zinkABSTRAKAplikasi Metode Inductively Coupled Plasma-Mass Spectrometry (ICP-MS) Dalam Analisis ZinkZink adalah salah satu jenis zat gizi yang sangat berpengaruh terhadap pertumbuhan sel, mengaktifkan sel T (limfosit T), regenerasi sel, dan membantu metabolisme tubuh. Zink di dalam tubuh setiap harinya mengalami proses ekskresi oleh karena itu asupan harian zink perlu diperhatikan untuk menjaga jumlah zink di dalam tubuh tetap dalam jumlah yang normal. Penelitian ini bertujuan untuk mendapatkan informasi penggunaan metode Inductively coupled plasma-mass spectrometry (ICP-MS) untuk menentukan konsentrasi zink dalam serum ibu hamil. Penggunaan metode ICP-MS dalam analisis zink memberikan keuntungan berupa kebutuhan volume sampel minimal dengan sensitivitas alat lebih tinggi, waktu retensi yang cepat serta memiliki batas limit deteksi konsentrasi hingga bagian per triliun (ppt). Analisis konsentrasi zink dalam serum ibu hamil dengan metode ICP-MS menunjukan 80% serum dengan konsentrasi dibawah nilai rujukan, 13,3% normal dan 6,7% konsentrasi yang lebih tinggi dibandingkan nilai rujukan menurut WHO.Kata kunci : defisiensi zink, inductively coupled plasma-mass spectrometry (icp-ms), zink
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50

Balaram, V. "Advances in Analytical Techniques and Applications in Exploration, Mining, Extraction, and Metallurgical Studies of Rare Earth Elements." Minerals 13, no. 8 (July 31, 2023): 1031. http://dx.doi.org/10.3390/min13081031.

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The use of analytical techniques is important and critical in all areas related to REE, such as basic fundamental research, exploration, mining, extraction, and metallurgical activities at different stages by different industries. At every stage of these activities, rock, ore, minerals, and other related materials have to be analyzed for their REE contents in terms of elemental, isotopic, and mineralogical concentrations using different analytical techniques. Spectacular developments have taken place in the area of analytical instrumentation during the last four decades, with some of them having shrunk in size and become handheld. Among laboratory-based techniques, F-AAS, GF-AAS, ICP-OES, and MP-AES have become very popular. Because of high sensitivity, fewer interference effects, and ease of use, ICP-MS techniques, such as quadrupole ICP-MS, ICP-MS/MS, ICP-TOF-MS, MH-ICP-MS, HR-ICP-MS, and MC-ICP-MS, with both solution nebulization as well as direct solid analysis using laser ablation sample introduction methods, have become more popular for REE analysis. For direct analysis of solids, INAA, XRF, and LIBS techniques, as well as LA-based ICP-MS techniques, are being extensively utilized. The LIBS technique in particular requires little to no sample preparation. TIMS, SIMS, and SHRIMP techniques are being used for isotopic as well as dating REE depots. Portable analytical techniques, such as pXRF, pLIBS, and Raman spectrometers are able to perform in situ analysis even in the field, helping to make fast decisions during exploration studies. At present, hyperspectral remote sensing techniques including handheld, drone, and satellite-based techniques have become very popular in REE exploration studies because of their ability to cover larger areas in a limited time and, thus, became very cost-effective. Deployment of microanalytical devices/sensors mounted in remotely operated vehicles (ROV) is being successfully utilized in detecting REE-rich deposits in the deep oceans. Providing updated in-depth information on all these important aspects with suitable examples, especially from the point of view of REE research studies is the focal point of this review article.
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