F42 Quantitative Energy-Dispersive Electron Probe X-ray Microanalysis of Individual Particles—Invited

2005 ◽  
Vol 20 (2) ◽  
pp. 186-186
Author(s):  
C.-U. Ro
2001 ◽  
Vol 30 (6) ◽  
pp. 419-426 ◽  
Author(s):  
J. Osán ◽  
J. de Hoog ◽  
P. Van Espen ◽  
I. Szalóki ◽  
C.-U. Ro ◽  
...  

2006 ◽  
Vol 21 (2) ◽  
pp. 140-144 ◽  
Author(s):  
Chul-Un Ro

An electron probe X-ray microanalysis (EPMA) technique using an energy-dispersive X-ray detector with an ultrathin window, designated low-Z particle EPM, has been developed. The low-Z particle EPMA allows the quantitative determination of concentrations of low-Z elements, such as C, N, and O, as well as higher-Z elements that can be analyzed by conventional energy-dispersive EPMA. The quantitative determination of low-Z elements (using full Monte Carlo simulations, from the electron impact to the X-ray detection) in individual environmental particles has improved the applicability of single-particle analysis, especially in atmospheric environmental aerosol research; many environmentally important atmospheric particles, e.g. sulfates, nitrates, ammonium, and carbonaceous particles, contain low-Z elements. The low-Z particle EPMA was applied to characterize loess soil particle samples of which the chemical compositions are well defined by the use of various bulk analytical methods. Chemical compositions of the loess samples obtained from the low-Z particle EPMA turn out to be close to those from bulk analyses. In addition, it is demonstrated that the technique can also be used to assess the heterogeneity of individual particles.


1982 ◽  
Vol 46 (341) ◽  
pp. 445-448 ◽  
Author(s):  
R. R. Harding ◽  
R. J. Merriman ◽  
P. H. A. Nancarrow

AbstractThe occurrence of three accessory minerals with significant rare earth contents in Tertiary acid rocks of St. Kilda is described. Allanite, zirkelite, and chevkinite were identified by electron probe analysis (with energy-dispersive attachment) and the chevkinite confirmed by X-ray diffraction. Brief comparison is made with other Tertiary occurrences of RE minerals. This is the first recorded occurrence of chevkinite in Great Britain.


2006 ◽  
Vol 12 (5) ◽  
pp. 406-415 ◽  
Author(s):  
Marco Alvisi ◽  
Markus Blome ◽  
Michael Griepentrog ◽  
Vasile-Dan Hodoroaba ◽  
Peter Karduck ◽  
...  

A calibration procedure for the detection efficiency of energy dispersive X-ray spectrometers (EDS) used in combination with scanning electron microscopy (SEM) for standardless electron probe microanalysis (EPMA) is presented. The procedure is based on the comparison of X-ray spectra from a reference material (RM) measured with the EDS to be calibrated and a reference EDS. The RM is certified by the line intensities in the X-ray spectrum recorded with a reference EDS and by its composition. The calibration of the reference EDS is performed using synchrotron radiation at the radiometry laboratory of the Physikalisch-Technische Bundesanstalt. Measurement of RM spectra and comparison of the specified line intensities enables a rapid efficiency calibration on most SEMs. The article reports on studies to prepare such a RM and on EDS calibration and proposes a methodology that could be implemented in current spectrometer software to enable the calibration with a minimum of operator assistance.


2013 ◽  
Vol 85 (21) ◽  
pp. 10424-10431 ◽  
Author(s):  
Hyo-Jin Eom ◽  
Hae-Jin Jung ◽  
Sophie Sobanska ◽  
Sang-Gwi Chung ◽  
Youn-Suk Son ◽  
...  

Author(s):  
Dale E. Newbury

Electron probe x-ray microanalysis (EPMA) with energy dispersive x-ray spectrometry (EDS) provides the capability for detecting elements with atomic number ≥ 4 (beryllium) from an excited specimen volume with linear dimensions of micrometers and a mass in the picogram range. To maximize the utility of EPMA/EDS, the analyst needs to understand the rich source of information that is potentially available in the x-ray spectrum. At its most basic level, interpretation of the spectrum consists of recognizing and identifying the various components of the spectrum as recorded by the EDS system: characteristic peaks, artifacts, and continuum background. While a modern EDS system is capable of making this interpretation in an automatic fashion, the careful analyst will always check the computer’s interpretation, which of course demands that the analyst be at least as "smart" as the computer! A systematic examination of spectra from pure elements or simple compounds is a good way to develop the necessary working knowledge.


2008 ◽  
Vol 14 (S2) ◽  
pp. 1152-1153
Author(s):  
K Keil ◽  
R Fitzgerald ◽  
KFJ Heinrich

Extended abstract of a paper presented at Microscopy and Microanalysis 2008 in Albuquerque, New Mexico, USA, August 3 – August 7, 2008


1998 ◽  
Vol 4 (S2) ◽  
pp. 184-185
Author(s):  
J. A. Small ◽  
J. A. Armstrong ◽  
D. S. Bright ◽  
B. B. Thorne

The addition of the Si-Li detector to the electron probe, the scanning electron microscope, and more recently the transmission electron microscope (resulting in the analytical electron microscope) has made it possible to obtain elemental analysis on individual “particles” with dimensions less than 1 nm using EDS. Although some initial particle studies on micrometer-sized particles were done on the electron probe using wavelength dispersive spectrometers, WDS, the variability and complexity of many particle compositions coupled with the high currents necessary for WDS made elemental analysis of particles by WDS difficult at best. In addition, the use of multiple spectrometers, each with a different view of the particle and therefore different particle geometry as shown in Fig. 1, limited the quantitative capabilities of the technique. With the introduction of the Si-Li detector, there was only one spectrometer with a single geometry resulting in the development of various procedures for obtaining quantitative elemental analysis of the individual particles.


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