Examples of Analysis from an Integrated X-Ray Fluorescence Analysis System Using NRLXRF

1982 ◽  
pp. 81-84
Author(s):  
B. E. Artz ◽  
M. J. Rokosz
1977 ◽  
Vol 21 ◽  
pp. 171-185 ◽  
Author(s):  
J.M. Jaklevic ◽  
W.R. French ◽  
T.W. Clarkson ◽  
M.R. Greenwood

We describe an adaptation of photon excited x-ray fluorescence analysis which is optimized for the analysis of small samples. A fine focus x-ray tube is used in conjunction with small diameter detector collimators in order to focus on a small sample volume with as high sensitivity as possible. Sample areas of less than 1 mm diameter can be analyzed with ppm detectability. In applications involving the analysis of human hair samples, a minimum detectable limit of 10 ppm Hg can be realized in a 1 mm long segment of a single hair in a counting time of 200 seconds. Simultaneous measurements of the sample mass can be obtained from the intensity of the incoherent scattering. An automated x-ray fluorescence analysis system using the technique for the scanning of elemental profiles in such hair samples will be described.


2015 ◽  
Vol 49 (3) ◽  
pp. 188-193 ◽  
Author(s):  
Shan Qing ◽  
Zhang XinLei ◽  
Zhang Yan ◽  
Jia WenBao ◽  
Ling YongSheng ◽  
...  

1981 ◽  
Vol 25 ◽  
pp. 81-84
Author(s):  
B. E. Artz ◽  
M. J. Rokosz

Methods of correction for matrix differences are required in X-ray Fluorescence (XRF) Analysis when the overall composition of the unknowns is substantially different from the available standards. Sample preparation techniques used to minimize matrix differences often require development time and can consume irreplaceable sample material. Alternatively, the increasing computer power available to the analyst and the refinement of computer programs using fundamental parameter calculations has made this approach more attractive.A system-consisting of a Siemens SRS-1 wavelength dispersive spectrometer (WDS), a KEVEX 0810-A/NS880 energy dispersive spectrometer (EDS), software for data collection and manipulation and a 40 element version of the NRLXRF fundamental-parameters analysis program has been put together to simplify XRF analysis of samples lacking standards of a similar composition. This configuration is shown schematically in Figure I.


1992 ◽  
Vol 63 (12) ◽  
pp. 5597-5601 ◽  
Author(s):  
Yasuji Muramatsu ◽  
Masaharu Oshima ◽  
Takashi Shoji ◽  
Hiroo Kato

1993 ◽  
Vol 302 ◽  
Author(s):  
Y.J. Wang ◽  
J.S. IWANCZYK

ABSTRACTA laboratory XRF analysis system employing an HgI2 spectrometer detector has been built. The system consists of an x-ray generator tube, a rotating carousel holding multiple XRF targets, and a probe head containing the HgI2 detector. Tests have been performed on several samples, under vacuum, helium and nitrogen ambient atmospheric conditions. This is of particular interest, since the applications for such an XRF system include operation under different ambient conditions. For applications in terrestrial and space planetary exploration, the expected temperatures and gas ambient will vary widely. Comparative analyses using the various gases were made on spectra obtained from standard geological samples.


1985 ◽  
Vol 29 ◽  
pp. 423-426 ◽  
Author(s):  
M. C. Nichols ◽  
R. W. Ryon

AbstractA prototype X-ray fluorescence system for chemical and phase microanalysis of materials has been developed and tested. Preliminary work with this system has indicated X-ray fluorescence detection limits on the order of 40 picograms for heavier elements such as gold when using a 100 micron collimator, 400 second counting time and a silver anode operating at 12 Kw. Phase identification by X- ray diffraction can be obtained from the same spot. A proposed design for an improved system providing greater elemental sensitivities and capable of semi-automated operation has been completed.


1971 ◽  
Vol 15 ◽  
pp. 228-239
Author(s):  
G. R. Dyer ◽  
D. A. Gedcke ◽  
T. R. Harris

X-ray fluorescence spectroscopy has been in use since the early days of the twentieth century, when Moseley confirmed the order of the chemical periodic table. However, fluorescence spectroscopy until recently has depended on diffraction methods to obtain sufficient resolution. Intrinsic resolution of ionization chambers, scintillation detectors, and proportional counters is inadequate for discrimination o f lines due to adjacent elements of low atomic number. The advent o f solid-state detectors, especially those using lithium-compensated silicon and low-noise electronics, has recently brought intrinsic energy resolution to the point where lines from adjacent elements as light as carbon and nitrogen can be resolved in theory; and detection of K radiation from elements as light as sodium is practical. Thus the solution to the long-standing problem of an adequate detector is at hand, and energy-dispersive spectrometers are now feasible.


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