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X-ray absorption
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Series: ASM Handbook Archive
Volume: 10
Publisher: ASM International
Published: 01 January 1986
DOI: 10.31399/asm.hb.v10.a0001764
EISBN: 978-1-62708-178-8
... Abstract This article provides an introduction to extended x-ray absorption fine structure (EXAFS). It describes the fundamentals of EXAFS with an emphasis on the physical mechanism, the single-scattering approximation, and multiple-scattering effects. The article discusses the use...
Abstract
This article provides an introduction to extended x-ray absorption fine structure (EXAFS). It describes the fundamentals of EXAFS with an emphasis on the physical mechanism, the single-scattering approximation, and multiple-scattering effects. The article discusses the use of synchrotron radiation as the x-ray source for EXAFS experiments. It also describes the typical EXAFS data analysis of pure nickel at 90 K, and explains the near-edge structure analysis of vanadium. The article presents a discussion on the unique features and applications of EXAFS.
Book Chapter
Series: ASM Handbook
Volume: 10
Publisher: ASM International
Published: 15 December 2019
DOI: 10.31399/asm.hb.v10.a0006665
EISBN: 978-1-62708-213-6
... Abstract This article provides a detailed account of extended x-ray absorption fine structure (EXAFS). It begins with a description of the fundamentals of EXAFS, providing information on the physical mechanism, single-scattering approximation, and multiple-scattering effects. This is followed...
Abstract
This article provides a detailed account of extended x-ray absorption fine structure (EXAFS). It begins with a description of the fundamentals of EXAFS, providing information on the physical mechanism, single-scattering approximation, and multiple-scattering effects. This is followed by a discussion on the use of synchrotron radiation as an X-ray source for EXAFS. Data-reduction procedures used to extract EXAFS signals are then described. The article also provides information on the analysis of x-ray absorption near-edge structure spectrum and ends with a discussion on the unique features and applications of EXAFS.
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Published: 01 January 1986
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Published: 15 December 2019
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Published: 15 December 2019
Fig. 1 Experimental extended x-ray absorption fine structure scan of nickel metal taken by using synchrotron radiation above the K-absorption edge of nickel at 8332.8 eV. The energy is labeled regarding the K-edge of nickel as zero.
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Published: 15 December 2019
Fig. 2 Experimental extended x-ray absorption fine structure scan of germanium in GeCl 4 molecule taken by using synchrotron radiation above the K-absorption edge of germanium at 11,103.3 eV. Source: Ref 13
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Published: 15 December 2019
Fig. 3 Experimental K-edge extended x-ray absorption fine structure spectrum of germanium in crystalline and glassy GeO 2 . The energy is labeled regarding the K-edge of germanium at 11,103.3 eV as zero. Source: Ref 15
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Published: 15 December 2019
Fig. 4 Schematic representation of extended x-ray absorption fine structure event. The excited electronic state is centered about the A-atom. The solid-line circles represent the crests of the outgoing part of the electronic state. The surrounding B-atoms backscatter the outgoing part
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Published: 15 December 2019
Fig. 6 Extended x-ray absorption fine structure experimental apparatus at the Stanford Synchrotron Radiation Laboratory. (a) Transmission mode of detection. (b) Fluorescence mode of detection. SPEAR, Stanford Position Electron Accelerator Ring. Source: Ref 35
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Published: 15 December 2019
Fig. 7 Typical extended x-ray absorption fine structure (EXAFS) data analysis. (a) Experimental scan of nickel K-edge EXAFS in pure nickel at 90 K. The broken line denotes a spline fit of the smooth post-edge background absorption above the absorption edge. (b) Normalized EXAFS plotted as χ
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Published: 15 December 2019
Fig. 8 Experimental (line) and simulated (points) extended x-ray absorption fine structure of the first shell of 12 neighbors from 1 to 2.8 Å about a nickel atom in face-centered cubic nickel at 90 K
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Published: 15 December 2019
Fig. 9 The vanadium K-edge x-ray absorption near-edge structure spectra of a series of vanadium oxides. The zero of energy is taken at the K-edge of vanadium metal at 5465 eV in all cases.
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Published: 15 December 2019
Fig. 12 Normalized nickel K-edge extended x-ray absorption fine structure plotted as χ · k versus k and corresponding Fourier transform. (a) Nickel impurity in synthetic diamond. (b) Face-centered cubic nickel. (c) Ni 3 B. r is the radial distance (phase shift not included) from
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in Characterization of Plastics in Failure Analysis
> Characterization and Failure Analysis of Plastics
Published: 15 May 2022
Fig. 5 Typical energy-dispersive x-ray spectroscopy spectrum showing absorption features indicative of unique elements and the quantitation of those elements. cps, counts per second
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Series: ASM Handbook
Volume: 13A
Publisher: ASM International
Published: 01 January 2003
DOI: 10.31399/asm.hb.v13a.a0003710
EISBN: 978-1-62708-182-5
... spectroscopy, Auger electron spectroscopy, X-ray photoelectron spectroscopy, ion scattering spectroscopy, reflectance Fourier transform infrared absorption spectroscopy, Raman and surface enhanced Raman spectroscopy, and extended X-ray absorption fine structure analysis. corrosion corrosion inhibition...
Abstract
This article describes the analytical methods for analyzing surfaces for corrosion and corrosion inhibition processes as well as failure analysis based on surface structure and chemical identity and composition. The principles and applications of the surface-structure analysis techniques, namely, optical microscopy, scanning electron microscopy, scanning tunneling microscopy, and atomic force microscopy, are reviewed. The article discusses the principles and applications of chemical identity and composition analysis techniques. These techniques include the energy dispersive X-ray spectroscopy, Auger electron spectroscopy, X-ray photoelectron spectroscopy, ion scattering spectroscopy, reflectance Fourier transform infrared absorption spectroscopy, Raman and surface enhanced Raman spectroscopy, and extended X-ray absorption fine structure analysis.
Series: ASM Handbook Archive
Volume: 10
Publisher: ASM International
Published: 01 January 1986
DOI: 10.31399/asm.hb.v10.a0001733
EISBN: 978-1-62708-178-8
... Abstract This article provides an introduction to x-ray spectrometry, and discusses the role of electromagnetic radiation, x-ray emission, and x-ray absorption. It focuses on the instrumentation of wavelength-dispersive x-ray spectrometers, and energy dispersive x-ray spectrometers (EDS...
Abstract
This article provides an introduction to x-ray spectrometry, and discusses the role of electromagnetic radiation, x-ray emission, and x-ray absorption. It focuses on the instrumentation of wavelength-dispersive x-ray spectrometers, and energy dispersive x-ray spectrometers (EDS) that comprise x-ray tubes, the analyzing system, and detectors. The fundamentals of EDS operation are described. The article also provides useful information on preparation of various samples, explaining the qualitative and quantitative analyses of EDS. It reviews the applications of the x-ray spectrometry.
Series: ASM Handbook
Volume: 10
Publisher: ASM International
Published: 15 December 2019
DOI: 10.31399/asm.hb.v10.a0006645
EISBN: 978-1-62708-213-6
...-dispersive spectrometer (WDS) and energy-dispersive spectrometer (EDS). This is followed by a discussion on the mechanism and effects of X-ray radiation, X-ray emission, and X-ray absorption. The article then discusses components used, operation, and applications of WDS and EDS. Some of the factors...
Abstract
This article provides a detailed account of X-ray spectroscopy used for elemental identification and determination. It begins with an overview of the operating principles of X-ray fluorescence (XRF) spectrometer, as well as a comparison of the operating principles of wavelength-dispersive spectrometer (WDS) and energy-dispersive spectrometer (EDS). This is followed by a discussion on the mechanism and effects of X-ray radiation, X-ray emission, and X-ray absorption. The article then discusses components used, operation, and applications of WDS and EDS. Some of the factors and processes involved in sample preparation for XRF analysis are also included. The article further provides information on the practical procedure for and the applications of WDS and EDS qualitative and quantitative analyses.
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Published: 15 December 2019
Fig. 10 Oxidation state versus energy positions of various absorption features in the vanadium K-edge x-ray absorption near-edge structure spectra of various vanadium oxides shown in Fig. 9
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Published: 15 December 2019
Fig. 11 Body-centered cubic (bcc) iron-nickel alloy containing 80 at.% Fe. (a) Experimental extended x-ray absorption fine structure (EXAFS) spectra above the K-edges of iron and nickel. (b) Normalized EXAFS plotted as χ · k versus k for the EXAFS. (c) Fourier transform of (b). The peaks
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Series: ASM Handbook Archive
Volume: 10
Publisher: ASM International
Published: 01 January 1986
DOI: 10.31399/asm.hb.v10.a0001757
EISBN: 978-1-62708-178-8
..., such as lattice parameter, absorption diffraction, spiking, and direct comparison, explaining where each may be used. It also identifies potential sources of error in XRPD measurements. cameras qualitative analysis quantitative analysis X-ray detectors X-ray powder diffraction Overview...
Abstract
X-ray powder diffraction (XRPD) techniques are used to characterize samples in the form of loose powders or aggregates of finely divided material that readily diffract x-rays in specified patterns. This article provides an introduction to XRPD, beginning with a review of sensing devices, including pinhole/Laue cameras, Debye-Scherrer/Gandolfi cameras, Guinier cameras, glancing angle cameras, conventional diffractometers, thin film diffractometers, Guinier diffractometers, and micro diffractometers. The article then describes several quantitative measurement methods, such as lattice parameter, absorption diffraction, spiking, and direct comparison, explaining where each may be used. It also identifies potential sources of error in XRPD measurements.
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