Analytical performance of benchtop total reflection X-ray fluorescence instrumentation for multielemental analysis of wine samples
Autor: | Fabjola Bilo, Laura Borgese, Eva Marguí, Laura E. Depero, Rogerta Dalipi |
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Přispěvatelé: | Ministerio de Economía y Competitividad (Espanya) |
Rok vydání: | 2016 |
Předmět: |
Accuracy and precision
Materials science Mo X-ray tube W X-ray tube Instrumentation Analytical chemistry X-ray fluorescence Wine Multielemental analysis TXRF Atomic and Molecular Physics and Optics Analytical Chemistry Spectroscopy 02 engineering and technology 01 natural sciences Atomic and Molecular Physics Inductively coupled plasma emission spectroscopy Detection limit Total internal reflection 010401 analytical chemistry Espectroscòpia de raigs X 021001 nanoscience & nanotechnology 0104 chemical sciences Photoelectron spectroscopy Espectroscòpia de fluorescència X-ray spectroscopy and Optics 0210 nano-technology |
Zdroj: | © Spectrochimica acta. Part B, Atomic spectroscopy, 2016, vol. 120, p. 37-43 Articles publicats (D-Q) DUGiDocs – Universitat de Girona instname |
ISSN: | 0584-8547 |
DOI: | 10.1016/j.sab.2016.04.001 |
Popis: | Recent technological improvements have led to a widespread adoption of benchtop total reflection X-ray fluorescence systems (TXRF) for analysis of liquid samples. However, benchtop TXRF systems usually present limited sensitivity compared with high-scale instrumentation which can restrict its application in some fields. The aim of the present work was to evaluate and compare the analytical capabilities of two TXRF systems, equipped with low power Mo and W target X-ray tubes, for multielemental analysis of wine samples. Using the Mo-TXRF system, the detection limits for most elements were one order of magnitude lower than those attained using the W-TXRF system. For the detection of high Z elements like Cd and Ag, however, W-TXRF remains a very good option due to the possibility of K-Lines detection. Accuracy and precision of the obtained results have been evaluated analyzing spiked real wine samples and comparing the TXRF results with those obtained by inductively coupled plasma emission spectroscopy (ICP-OES). In general, good agreement was obtained between ICP-OES and TXRF results for the analysis of both red and white wine samples except for light elements (i.e., K) which TXRF concentrations were underestimated. However, a further achievement of analytical quality of TXRF results can be achieved if wine analysis is performed after dilution of the sample with de-ionized water Thisworkwas supported by the Spanish National Research Program (Project ref. CGL2013-48802-C3-2-R) |
Databáze: | OpenAIRE |
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