Hostname: page-component-7bb8b95d7b-495rp Total loading time: 0 Render date: 2024-10-04T16:19:36.108Z Has data issue: false hasContentIssue false

Importance of Carbon Contamination in High-Resolution (FEG) EPMA of Silicate Minerals

Published online by Cambridge University Press:  16 April 2015

Ben Buse*
Affiliation:
School of Earth Sciences, University of Bristol, Bristol, BS8 1RJ, UK
Stuart Kearns
Affiliation:
School of Earth Sciences, University of Bristol, Bristol, BS8 1RJ, UK
*
*Corresponding author.ben.buse@bristol.ac.uk
Get access

Abstract

The effect of carbon contamination on the analysis of carbon-coated silicate minerals at 5 kV for X-ray energies 0.7–4 keV is examined. For individual spot analyses, carbon is found to deposit adjacent to the beam spot forming ring-shaped deposits with no impact on the analysis. Carbon contamination becomes important for closely spaced analyses such as multipoint transects, where each subsequent analysis overlaps the carbon ring of the previous analysis. X-ray intensity loss due to contamination is most severe for low-overvoltage elements such as Ca K consistent with carbon deposition effectively reducing beam energy. Rates of contamination are calculated and the use of a liquid nitrogen cold trap is shown to greatly reduce the amount of carbon deposited. A complimentary empirical correction is developed to correct for X-ray intensity loss from measured carbon, assuming the carbon is a film, and is compared with corrections derived from thin film calculations. PENELOPE electron probe microanalysis (PENEPMA) calculations confirm that asymmetry of the carbon deposition can be ignored for X-ray energies where intensity loss is predominantly through energy loss of beam electrons. Using a cold trap and/or an empirical correction high spatial resolution analysis (ca. 400 nm between points) is achievable with analytical errors of ca. 1–3%.

Type
Materials Applications
Copyright
© Microscopy Society of America 2015 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Armstrong, L.S., Walter, M., Tuff, J., Lord, O., Lennie, A., Kleppe, A. & Clark, . (2012). Pervoskite phase relations in the system CaO-MgO-TiO2-SiO2 and implications for deep mantle lithologies. J Petrol 53, 611635.CrossRefGoogle Scholar
Augustyn, E., Hallstedt, B., Wietbrock, B., Mayer, J., Schwedt, A. & Richter, S. (2012). Chemical characterisation of scale formation of high manganese steels (Fe-Mn23-C0.6) on the sub-micrometre scale: A challenge for EPMA. IOP Conf Ser: Mater Sci Eng 32, 012001.CrossRefGoogle Scholar
Bastin, G.F. & Heijligers, H.J.M. (1988). Contamination phenomena in the electron probe microanalyzer. In Microbeam Analysis, Newbury, D.E. (Ed.), pp. 325328. San Francisco, USA: San Francisco Press.Google Scholar
Bastin, G.F. & Heijligers, H.J.M. (1990 a). Quantitative Electron Probe Microanalysis of Carbon in Binary Carbides. Internal Report, Eindhoven University of Technology.Google Scholar
Bastin, G.F. & Heijligers, H.J.M. (1990 b). Quantitative electron probe microanalysis of ultralight elements (boron-oxygen). Scanning 12, 225236.CrossRefGoogle Scholar
Duerr, J.S. & Ogilvie, R.E. (1972). Electron probe microdetermination of carbon in ferrous alloys. Anal Chem 44, 23612367.CrossRefGoogle Scholar
Fialin, M., Catillon, G. & Andrault, D. (2009). Disproportionation of Fe2+ in Al-free silicate perovskite in the laser heater diamond anvil cell as recorded by electron probe microanalysis of oxygen. Phys Chem Minerals 36, 183191.CrossRefGoogle Scholar
Fujino, K., Sasaki, Y., Komori, T., Ogawa, H., Miyajima, N., Sata, N. & Yagi, T. (2004). Approach to the mineralogy of the lower mantle by a combined method of a laser-heated diamond anvil cell experiment and analytical electron microscopy. Phys Earth Planet In 143–144, 215221.CrossRefGoogle Scholar
Gopon, P., Fournelle, J., Sobol, P.E. & Llovet, X. (2013). Low-voltage electron-probe microanalysis of Fe-Si compounds using soft X-rays. Microsc Microanal 19, 16981708.CrossRefGoogle ScholarPubMed
Hirsch, P., Kassens, M., Puttmann, M. & Reimer, L. (1994). Contamination in a scanning electron microscope and the influence of specimen cooling. Scanning 16, 101110.CrossRefGoogle Scholar
Isabell, T.C., Fischione, P.E., O’Keefe, C., Guruz, M.U. & Dravid, V.P. (1999). Plasma cleaning and its applications for electron microscopy. Microsc Microanal 5, 126135.CrossRefGoogle ScholarPubMed
Kerrick, D.M., Eminhizer, L.B. and Villaume, J.F. (1973). The role of carbon film thickness in electron microprobe analysis. Am Mineral 58, 920925.Google Scholar
Limandri, S.P., Silvina, P., Carreras, Alejo, C., Trincavelli, & Jorge, C. (2010). Effects of the carbon coating and the surface oxide layer in electron probe microanalysis. Microsc Microanal 16, 583593.CrossRefGoogle ScholarPubMed
Llovet, X., Fernandez-Varea, J.M., Sempau, J. & Salvat, F. (2005). Monte Carlo simulation of X-ray emission using the general-purpose code PENELOPE. Surf Interface Anal 37, 10541058.CrossRefGoogle Scholar
McSwiggen, P. (2014). Characterisation of sub-micrometre features with the FE-EPMA. IOP Conf Ser: Mater Sci Eng 55, 012009.CrossRefGoogle Scholar
Osada, Y. (2005). Monte Carlo study of quantitative EPMA analysis of a non-conducting sample with a coating film. X-Ray Spectrom 34, 96100.CrossRefGoogle Scholar
Pinard, P.T., Schwedt, A., Ramazani, A., Prahl, U. & Richter, S. (2013 a). Characterization of dual-phase steel microstructure by combined submicrometer EBSD and EPMA carbon measurements. Microsc Microanal 19, 9961006.CrossRefGoogle ScholarPubMed
Pinard, P.T., Demers, H., Gauvin, R. & Richter, S. (2013 b). High resolution carbon measurements in steel using FE-EPMA. EMAS 2013 Conference Abstract.Google Scholar
Pouchou, J.L. (2002). X-Ray Microanalysis of Thin Surface Films and Coatings. Mikrochim. Acta 138, 133152.CrossRefGoogle Scholar
Pouchou, J.L. & Pichoir, F. (1990). Surface film X-ray microanalysis. Scanning 12, 212224.CrossRefGoogle Scholar
Reed, S.J.B. (1975). Electron Microprobe Analysis. Cambridge, UK: Cambridge University Press.Google Scholar
Reimer, L. & Wächter, M. (1978). Contribution to the contamination problem in transmission electron microscopy. Ultramicroscopy 3, 169174.CrossRefGoogle Scholar
Saunders, K., Buse, B., Kilburn, M.R., Kearns, S. & Blundy, J. (2014). Nanoscale characterisation of crystal zoning. Chem Geol 364, 2032.CrossRefGoogle Scholar
Spray, J.G. & Rae, D.A. (1995). Quantitative electron-microprobe analysis of alkali silicate glasses: A review and user guide. Can Mineral 33, 323332.Google Scholar
Waldo, R.A. (1988). An iteration procedure to calculate film compositions and thicknesses in electron-probe microanalysis. Microbeam Analysis, 310314.Google Scholar
Wendt, M. (1980). The role of contamination layers in electron probe microanalysis. Krist Tech 15, 13671375.CrossRefGoogle Scholar