scholarly journals Solving self-absorption in fluorescence

IUCrJ ◽  
2019 ◽  
Vol 6 (4) ◽  
pp. 586-602 ◽  
Author(s):  
Ryan M. Trevorah ◽  
Christopher T. Chantler ◽  
Martin J. Schalken
Keyword(s):  
Software Package ◽  
Experimental Approach ◽  
Experimental Investigations ◽  
Accuracy Analysis ◽  
X Ray ◽  
Fluorescence Photon ◽  
Wide Range ◽  
Self Consistent ◽  
Consistent Method ◽  
X Ray Absorption

One of the most common types of experiment in X-ray absorption spectroscopy (XAS) measures the secondary inelastically scattered fluorescence photon. This widespread approach has a dominant systematic of self-absorption of the fluorescence photon. The large impact of self-absorption compromises accuracy, analysis and insight. Presented here is a detailed self-consistent method to correct for self-absorption and attenuation in fluorescence X-ray measurements. This method and the resulting software package can be applied to any fluorescence data, for XAS or any other experimental approach detecting fluorescence or inelastically scattered radiation, leading to a general solution applicable to a wide range of experimental investigations. The high intrinsic accuracy of the processed data allows these features to be well modelled and yields deeper potential insight.

scholarly journals MEASURING DISPLACEMENT AND VELOCITY OF A STRIKER USING A RADIO-INTERFEROMETER

2019 ◽  
Vol 81 (1) ◽  
pp. 118-128
Author(s):  
V. V. Balandin ◽  
V. V. Balandin ◽  
V. V. Parkhachev
Keyword(s):  
High Speed ◽  
Radio Interferometer ◽  
Experimental Investigations ◽  
X Ray ◽  
Gas Gun ◽  
Impact Interaction ◽  
Ballistic Experiment ◽  
Wide Range ◽  
Series Of Experiments ◽  
Error Of Measurement

Investigating impact interaction of solid and deformed bodies with obstacles of various physical natures requires developing experimental methodologies of registering the parameters of the interaction process. In experimental investigations of impact interaction of solids, it is common practice to measure displacement of strikers as a function of time, as well as their velocity and deceleration. To determine the displacement and velocity of a striker, a radio-interferometric methodology of registering the displacement of its rear end is proposed. In contrast with the registration methods based on high-speed filming and pulsed X-ray photography, the method using a millimeter-range radio-interferometer provides continuous high-accuracy registering of the displacement of the rear end of a striker in a wide range of displacement values. To test the effectiveness of the methodology, a series of experiments have been conducted on registering the motion of a cylindrical striker of an aluminum alloy, fired from a 20mm-dia gas gun. The displacement of the striker was also monitored using high-speed filming. The results of measuring using the two methodologies differ within the limits of the error of measurement. Based on the results of the above experiments, it has been concluded that the methodology of determining the displacement and velocity of strikers in a ballistic experiment using a mm-range radio-interferometer makes it possible to measure practically continuously large displacements (100 mm and larger) to a safe accuracy. The present methodology can be used for measuring the displacement and velocity of the rear end of a striker interacting with obstacles of various physical natures (metals, ceramics, soils, concretes, etc.).

Near Edge X-Ray Absorption Fine Structure (NEXAFS) Microscopy: Chemical Analysis at Sub Visible Spatial Resolution

1997 ◽  
Vol 3 (S2) ◽  
pp. 851-852
Author(s):  
H. Ade
Keyword(s):  
Fine Structure ◽  
Compositional Analysis ◽  
High Sensitivity ◽  
Linear Dichroism ◽  
X Rays ◽  
X Ray ◽  
Absorption Fine ◽  
Nexafs Spectroscopy ◽  
Wide Range ◽  
X Ray Absorption

Infrared, Raman, and fluorescence/luminescence microspectroscopy/microscopy in many instances seek to provide high sensitivity compositional and functional information that goes beyond mere elemental composition. This goal is shared by NEXAFS microscopy, in which Near Edge X-ray Absorption Fine Structure (NEXAFS) spectroscopy is employed to provide chemical sensitivity and can be relatively easily adopted in a scanning transmission x-ray microscope (STXM). In addition to compositional information, NEXAFS microscopy can exploit the dependence of x-ray absorption resonances on the bond orientation relative to the linearly polarized x rays (linear dichroism microscopy). For compositional analysis, NEXAFS microscopy is analogous to Electron Energy Loss Spectroscopy (EELS) in an electron microscope. However, when utilizing near edge spectral features, NEXAFS microscopy requires a considerable lower dose than EELS microscopy which makes it very suitable to studying radiation sensitive materials such as polymers. NEXAFS has shown to have excellent sensitivity to a wide range of moieties in polymers, including sensitivity to substitution isomerism.

Phosphorus L 2,3-edge XANES: overview of reference compounds

2009 ◽  
Vol 16 (2) ◽  
pp. 247-259 ◽  
Author(s):  
Jens Kruse ◽  
Peter Leinweber ◽  
Kai-Uwe Eckhardt ◽  
Frauke Godlinski ◽  
Yongfeng Hu ◽  
...  
Keyword(s):  
Spectral Features ◽  
Edge Structure ◽  
Complex Samples ◽  
Distinctive Features ◽  
X Ray ◽  
Wide Range ◽  
Element Speciation ◽  
Unknown Composition ◽  
Almost All ◽  
X Ray Absorption

Synchrotron-based X-ray absorption near-edge structure (XANES) spectroscopy is becoming an increasingly used tool for the element speciation in complex samples. For phosphorus (P) almost all XANES measurements have been carried out at the K-edge. The small number of distinctive features at the P K-edge makes in some cases the identification of different P forms difficult or impossible. As indicated by a few previous studies, the P L 2,3-edge spectra were richer in spectral features than those of the P K-edge. However, experimentally consistent spectra of a wide range of reference compounds have not been published so far. In this study a library of spectral features is presented for a number of mineral P, organic P and P-bearing minerals for fingerprinting identification. Furthermore, the effect of radiation damage is shown for three compounds and measures are proposed to reduce it. The spectra library provided lays a basis for the identification of individual P forms in samples of unknown composition for a variety of scientific areas.

Microstructure of TiC/Amorphous Hydrocarbon Nanocomposite Coatings

2000 ◽  
Vol 6 (S2) ◽  
pp. 440-441
Author(s):  
D. M. Cao ◽  
J. C. Jiang ◽  
B. Feng ◽  
W. J. Meng
Keyword(s):  
Inductively Coupled Plasma ◽  
High Hardness ◽  
Ceramic Surface ◽  
Edge Structure ◽  
X Ray ◽  
Inductively Coupled ◽  
Transmission Electron ◽  
Wide Range ◽  
Mechanical Components ◽  
X Ray Absorption

Application of an appropriate ceramic surface coating to mechanical components such as bearings and gears can provide longer life and increased performance reliability. Metal-containing hydrocarbon (Me-C:H) coatings possess high hardness, together with low friction and low wear rate. They have also been suggested to adhere better to metallic substrates. This combination of attractive mechanical/tribological properties makes Me-C:H coatings potentially useful for surface modification of a wide range of mechanical components.Using the technique of inductively coupled plasma (ICP) assisted vapor deposition[1], we have synthesized Ti-containing hydrocarbon (Ti-C:H) coatings with a wide range of Ti compositions[2]. Coating mechanical properties such as modulus and hardness have been measured by the technique of nanoindentation and correlated to Ti and hydrogen compositions[2,3].We have performed detailed microstructural examination of Ti-C:H coatings by transmission electron microscopy (TEM), Extended X-ray Absorption Fine Structure (EXAFS) spectroscopy, and X-ray Absorption Near Edge Structure (XANES) spectroscopy.

In Situ Synchrotron X-ray Absorption Experiments and Modelling of the Growth Rates of Electrochemically Deposited ZnO Nanostructures

2007 ◽  
Vol 1017 ◽  
Author(s):  
Bridget Ingham ◽  
Benoit N. Illy ◽  
Jade R. Mackay ◽  
Stephen P. White ◽  
Shaun C. Hendy ◽  
...  
Keyword(s):  
Growth Rates ◽  
High Resolution Electron Microscopy ◽  
Ex Situ ◽  
X Ray ◽  
Deposition Parameters ◽  
Wide Range ◽  
Electrochemically Deposited ◽  
Electrochemical Current ◽  
X Ray Absorption

AbstractZnO is known to produce a wide variety of nanostructures that have enormous scope for optoelectronic applications. Using an aqueous electrochemical deposition technique, we are able to tightly control a wide range of deposition parameters (Zn2+ concentration, temperature, potential, time) and hence the resulting deposit morphology. By simultaneously conducting synchrotron x-ray absorption spectroscopy (XAS) experiments during the deposition, we are able to directly monitor the growth rates of the nanostructures, as well as providing direct chemical speciation of the films. In situ experiments such as these are critical to understanding the nucleation and growth of such nanostructures.Recent results from in situ XAS synchrotron experiments demonstrate the growth rates as a function of potential and Zn2+ concentration. These are compared with the electrochemical current density recorded during the deposition, and the final morphology revealed through ex situ high resolution electron microscopy. The results are indicative of two distinct growth regimes, and simultaneous changes in the morphology are observed.These experiments are complemented by modelling the growth of the rods in the transport-limited case, using the Nernst-Planck equations in 2 dimensions, to yield the growth rate of the volume, length, and radius as a function of time.

scholarly journals Experimental Investigations of the Interaction of SO2 with MgO

1999 ◽  
Vol 590 ◽  
Author(s):  
Andrea Freitag ◽  
J. A. Rodriguez ◽  
J. Z. Larese
Keyword(s):  
High Resolution ◽  
Film Thickness ◽  
Room Temperature ◽  
Temperature Programmed Desorption ◽  
Experimental Investigations ◽  
X Ray Diffraction ◽  
High Quality ◽  
X Ray ◽  
Temperature Programmed ◽  
X Ray Absorption

ABSTRACTHigh resolution adsorption isotherms, temperature programmed desorption (TPD), x-ray diffraction (XRD) and x-ray absorption near edge spectroscopy (XANES) methods were used to investigate the interaction of SO2 with high quality MgO powders. The results of these investigations indicate that when SO2 is deposited on MgO in monolayer quantities at temperatures near 100K both SO3 and SO4 species form that are not removed by simply pumping on the pre-dosed samples at room temperature. TPD and XANES studies indicate that heating of pre-dosed MgO samples to temperatures above 350 °C is required for full removal of the SO3/SO4 species. XANES measurements made as a function of film thickness indicate for coverages near monolayer completion that the SO4 species form first.

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