A 2D imaging detector system for X-ray fluorescence analysis

1990 ◽  
Vol 299 (1-3) ◽  
pp. 567-570
Author(s):  
Masaki Koike ◽  
Isao H. Suzuki ◽  
Sigeru Nakae ◽  
Ken-ichi Hasegawa
Keyword(s):  
Fluorescence Analysis ◽  
Detector System ◽  
X Ray ◽  
Imaging Detector ◽  
2D Imaging

scholarly journals HEXITEC 2 × 2 tiled hard X-ray spectroscopic imaging detector system

2022 ◽  
Vol 17 (01) ◽  
pp. P01012
Author(s):  
L. Jowitt ◽  
M. Wilson ◽  
P. Seller ◽  
C. Angelsen ◽  
R.M. Wheater ◽  
...  
Keyword(s):  
Spectroscopic Imaging ◽  
Detector System ◽  
Frame Rate ◽  
Energy Curve ◽  
Charge Sharing ◽  
Camera System ◽  
X Ray ◽  
Sensor Material ◽  
Imaging Detector ◽  
Sealed Source

Abstract HEXITEC is a spectroscopic imaging X-ray detector technology developed at the STFC Rutherford Appleton Laboratory for X-ray and γ-ray spectroscopic imaging applications. Each module has 80 × 80 pixels on a 250 μm pixel pitch, and has been implemented successfully in a number of applications. This paper presents the HEXITEC 2 × 2 detector system, a tiled array of 4 HEXITEC modules read out simultaneously, which provides an active area of 16 cm2. Systems have been produced using 1 mm thick Cadmium Telluride (CdTe) and 2 mm thick Cadmium Zinc Telluride (CdZnTe) sensor material. In this paper the system and data processing methods are presented, and the performance of the systems are evaluated. The detectors were energy calibrated using an 241Am sealed source. Three types of charge sharing correction were applied to the data-charge sharing addition (CSA), charge sharing discrimination (CSD), and energy curve correction (ECC) which compensates for energy lost in the inter-pixel region. ECC recovers an additional 34 % of counts in the 59.5 keV peak in CdTe compared to the use of CSD; an important improvement for photon-starved applications. Due to the high frame rate of the camera system (6.3 kHz) an additional End of Frame (EOF) correction was also applied to 6.0 % of events to correct for signals that were readout whilst the signal was still forming. After correction, both detector materials were found to have excellent spectroscopic performance with a mean energy resolution (FWHM) of 1.17 keV and 1.16 keV for CdZnTe and CdTe respectively. These results successfully demonstrate the ability to construct tiled arrays of HEXITEC modules to provide larger imaging areas.

Versatile high-resolution imaging detector system for use in x-ray, EUV, and visible wavelength regions

1995 ◽  
Author(s):  
Peter D. Read ◽  
Martin K. Carter ◽  
Barry J. Kent ◽  
Bruce M. Swinyard ◽  
B. E. Patchett ◽  
...  
Keyword(s):  
High Resolution ◽  
Detector System ◽  
High Resolution Imaging ◽  
X Ray ◽  
Visible Wavelength ◽  
Imaging Detector ◽  
Resolution Imaging

An x-ray microprobe based upon a close-coupled focal-spot / glass capillary arrangement

1992 ◽  
Vol 50 (2) ◽  
pp. 1758-1759
Author(s):  
D. A. Carpenter ◽  
M. A. Taylor
Keyword(s):  
Imaging Techniques ◽  
Fluorescence Analysis ◽  
High Sensitivity ◽  
Specimen Preparation ◽  
X Rays ◽  
Glass Capillary ◽  
Close Coupling ◽  
X Ray ◽  
Point To Point ◽  
Beam Damage

The development of intense sources of x rays has led to renewed interest in the use of microbeams of x rays in x-ray fluorescence analysis. Sparks pointed out that the use of x rays as a probe offered the advantages of high sensitivity, low detection limits, low beam damage, and large penetration depths with minimal specimen preparation or perturbation. In addition, the option of air operation provided special advantages for examination of hydrated systems or for nondestructive microanalysis of large specimens.The disadvantages of synchrotron sources prompted the development of laboratory-based instrumentation with various schemes to maximize the beam flux while maintaining small point-to-point resolution. Nichols and Ryon developed a microprobe using a rotating anode source and a modified microdiffractometer. Cross and Wherry showed that by close-coupling the x-ray source, specimen, and detector, good intensities could be obtained for beam sizes between 30 and 100μm. More importantly, both groups combined specimen scanning with modern imaging techniques for rapid element mapping.

XRMF applications of a monolithic, polycapillary, focusing x-ray optic

1996 ◽  
Vol 54 ◽  
pp. 240-241
Author(s):  
D. A. Carpenter ◽  
Ning Gao ◽  
G. J. Havrilla
Keyword(s):  
Trace Elements ◽  
Point Source ◽  
Focal Spot ◽  
Fluorescence Analysis ◽  
X Rays ◽  
Focal Distance ◽  
Spot Diameter ◽  
X Ray ◽  
Focal Spot Diameter

A monolithic, polycapillary, x-ray optic was adapted to a laboratory-based x-ray microprobe to evaluate the potential of the optic for x-ray micro fluorescence analysis. The polycapillary was capable of collecting x-rays over a 6 degree angle from a point source and focusing them to a spot approximately 40 µm diameter. The high intensities expected from this capillary should be useful for determining and mapping minor to trace elements in materials. Fig. 1 shows a sketch of the capillary with important dimensions.The microprobe had previously been used with straight and with tapered monocapillaries. Alignment of the monocapillaries with the focal spot was accomplished by electromagnetically scanning the focal spot over the beveled anode. With the polycapillary it was also necessary to manually adjust the distance between the focal spot and the polycapillary.The focal distance and focal spot diameter of the polycapillary were determined from a series of edge scans.

Sorption of Se (IV) from aqueous solutions with subsequent determination by X-ray fluorescence analysis

2020 ◽  
Vol 86 (10) ◽  
pp. 5-9
Author(s):  
D. G. Filatova ◽  
A. A. Arkhipenko ◽  
M. A. Statkus ◽  
V. V. Es’kina ◽  
V. B. Baranovskaya ◽  
...  
Keyword(s):  
Inductively Coupled Plasma ◽  
Fluorescence Analysis ◽  
Standard Samples ◽  
Phase Contact Time ◽  
Sorbent Phase ◽  
X Ray ◽  
Fundamental Parameters ◽  
Inductively Coupled ◽  
Subsequent Determination

An approach to sorptive separation of Se (IV) from solutions on a novel S,N-containing sorbent with subsequent determination of the analyte in the sorbent phase by micro-x-ray fluorescence method is presented. The sorbent copolymethylenesulfide-N-alkyl-methylenamine (CMA) was synthesized using «snake in the cage» procedure and proven to be stable in acid solutions. Conditions for quantitative extraction of Se (IV) were determined: sorption in 5 M HCl or 0.05 M HNO3 solutions when heated to 60°C, phase contact time being 1 h. The residual selenium content in the solution was determined by inductively coupled plasma mass spectrometry (ICP-MS) using 82Se isotope. The absence of selenium losses is proved and the mechanism of sorption interaction under specified conditions is proposed. The method of micro-x-ray fluorescence analysis (micro-RFA) with mapping revealed a uniform distribution of selenium on the sorbent surface. The possibility of determining selenium in the sorbent phase by micro-RFA is shown. When comparing the obtained results with the results of calculations by the method of fundamental parameters, it is shown the necessity of using standard samples of sorbates to obtain correct results of RFA determination of selenium in the sorbent phase.

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