Background reduction of x-ray fluorescence spectra in a secondary target energy dispersive spectrometer

1979 ◽  
Vol 165 (1) ◽  
pp. 63-65 ◽  
Author(s):  
P. Standzenieks ◽  
E. Selin
1986 ◽  
Vol 15 (4) ◽  
pp. 231-238 ◽  
Author(s):  
Peter Van Dyck ◽  
Szabina Török ◽  
René Van Grieken

Author(s):  
J. Bentley ◽  
E. A. Kenik

Instruments combining a 100 kV transmission electron microscope (TEM) with scanning transmission (STEM), secondary electron (SEM) and x-ray energy dispersive spectrometer (EDS) attachments to give analytical capabilities are becoming increasingly available and useful. Some typical applications in the field of materials science which make use of the small probe size and thin specimen geometry are the chemical analysis of small precipitates contained within a thin foil and the measurement of chemical concentration profiles near microstructural features such as grain boundaries, point defect clusters, dislocations, or precipitates. Quantitative x-ray analysis of bulk samples using EDS on a conventional SEM is reasonably well established, but much less work has been performed on thin metal foils using the higher accelerating voltages available in TEM based instruments.


2007 ◽  
Vol 62 (1) ◽  
pp. 63-68 ◽  
Author(s):  
V.A. Solé ◽  
E. Papillon ◽  
M. Cotte ◽  
Ph. Walter ◽  
J. Susini

1989 ◽  
Vol 158 (1-3) ◽  
pp. 317-321 ◽  
Author(s):  
H. Tolentino ◽  
E. Dartyge ◽  
A. Fontaine ◽  
G. Tourillon

1982 ◽  
Vol 26 ◽  
pp. 369-376 ◽  
Author(s):  
Ronald A. Vane

The XRF11 program by John Criss and the EXACT program are two commercially available fundamental parameters programs for energy dispersive x-ray fluorescence spectrometry (EDXRF). These programs are both based on the same underlying equations but use different approaches to the calculations. The EXACT program assumes monochromatic excitation, and the XEF11 program models polychromatic excitation sources. There are also great differences in how the two programs approach the iterations in the calculations and in how the data from standards are used in the two programs for calibration.To produce the monochromatic excitation neeiled by the EXACT program, secondary targets have been the preferred method. But it is also possible to approximate monochromatic excitation by using filtered direct excitation. The purpose of this study is to compare the data obtained from both secondary targets and direct filtered excitation as processed through both XRF11 and EXACT.


1993 ◽  
Vol 37 ◽  
pp. 667-675
Author(s):  
Walter Swoboda ◽  
Burkhard Beckhoff ◽  
Birgit Kanngieβer ◽  
J. Scheer

The scattering of the primary X-ray tube spectrum on a low Z material in 90°-geometry produces polarised excitation radiation, which clearly decreases the background of fluorescence spectra in Cartesian geometry (Barkla excitation). Several publications have shown the advantages of this excitation mode in comparison with both direct excitation and secondary target excitation.


1992 ◽  
Vol 263 (6) ◽  
pp. H1946-H1957 ◽  
Author(s):  
H. Mori ◽  
S. Haruyama ◽  
Y. Shinozaki ◽  
H. Okino ◽  
A. Iida ◽  
...  

We developed new nonradioactive microspheres and used more sensitive X-ray fluorescence spectrometers than used previously to measure regional blood flow in the heart and other organs. We demonstrated the chemical stability of eight kinds of heavy element-loaded microspheres and validated their use for regional blood flow measurement by comparing duplicate flows measured with radioactive and/or nonradioactive microspheres in both acute and chronic dog experiments. The wavelength-dispersive spectrometer (Philips PW 1480) has a higher sensitivity than the previously described X-ray fluorescent system and reduced the number of microspheres required for accurate measurement. The fine energy resolution of this system makes it possible to increase the numbers of different kinds of microspheres to be quantitated, but at present only eight kinds are available. We also used a synchrotron radiation-excited energy dispersive spectrometer. The monochromatic synchrotron radiation allowed us to obtain much higher signal-to-background ratios of X-ray fluorescence spectra than with the wavelength-dispersive system (50 dB more for Zr-loaded microspheres) and will enable analysis of fluorescent activity in smaller regions (< 20 mg) than the radioactive method does.


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