High-resolution coded-aperture design for compressive X-ray tomography using low resolution detectors

2017 ◽  
Vol 404 ◽  
pp. 103-109 ◽  
Author(s):  
Edson Mojica ◽  
Said Pertuz ◽  
Henry Arguello
2007 ◽  
Vol 40 (6) ◽  
pp. 1123-1134 ◽  
Author(s):  
Helmut Durchschlag ◽  
Peter Zipper ◽  
Angelika Krebs

The technique of small-angle scattering can be used advantageously for deriving the shape of proteins in solution. Presently, advancedab initioapproaches allow the reliable automated reconstruction of particle shapes. In particular, the procedures based on simulated annealing such asDAMMINin combination with tight constraints turn out to be highly qualified for establishing realistic models. The appearance of the models, the comparison of experimental and calculated scattering profiles, and the agreement of both structural and hydrodynamic parameters can be used as evaluation criteria. In addition, the comparison of the SAXS-based low-resolution models with high-resolution crystal structures allows the models under analysis to be checked. Superimposing the SAXS models and the crystallographic structures yields evidence for the validity of the SAXS-derived models and far-reaching agreement of the protein structure in the crystal and in solution, both in the case of small molecules and giant multisubunit proteins, and for proteins of quite different shape. Modelling of molecules requires application of a variety of sophisticated approaches and consideration of several precautions. These include the use of substitutes for amino-acid residues missing in the crystallographic databases, application of special aligning, superimposing, filtering and averaging procedures, drastic reduction of the enormous number of beads to be used for modelling large molecules from crystal data, and the application of hydration contributions. Reconstructions of low-resolution SAXS-based shapes and comparisons with high-resolution X-ray structures were performed with glycogen phosphorylase, citrate synthase and an annelid haemoglobin. In the latter case, both the dodecameric subunit and the giant 3.5 MDa complex were studied, together with reconstructions of hypothetical complexes from building blocks.


2004 ◽  
Vol 22 (3) ◽  
pp. 373-379 ◽  
Author(s):  
ANATOLY FAENOV ◽  
TATIANA PIKUZ ◽  
ALEXANDER MAGUNOV ◽  
DIMITRI BATANI ◽  
GIANNI LUCCHINI ◽  
...  

We present some experimental results on X-ray spectra obtained from plasmas produced using a compact Nd:YAG laser system. The beam was focused on different targets (Cu, Al, Ge,…) and both high resolution and low resolution X-ray spectra were recorded.


2013 ◽  
Vol 16 (04) ◽  
pp. 353-368 ◽  
Author(s):  
A.. Dehghan Khalili ◽  
J.-Y.. -Y. Arns ◽  
F.. Hussain ◽  
Y.. Cinar ◽  
W.V.. V. Pinczewski ◽  
...  

Summary High-resolution X-ray-computed-tomography (CT) images are increasingly used to numerically derive petrophysical properties of interest at the pore scale—in particular, effective permeability. Current micro-X-ray-CT facilities typically offer a resolution of a few microns per voxel, resulting in a field of view of approximately 5 mm3 for a 2,0482 charge-coupled device. At this scale, the resolution is normally sufficient to resolve pore-space connectivity and calculate transport properties directly. For samples exhibiting heterogeneity above the field of view of such a single high-resolution tomogram with resolved pore space, a second low-resolution tomogram can provide a larger-scale porosity map. This low-resolution X-ray-CT image provides the correlation structure of porosity at an intermediate scale, for which high-resolution permeability calculations can be carried out, forming the basis for upscaling methods dealing with correlated heterogeneity. In this study, we characterize spatial heterogeneity by use of overlapping registered X-ray-CT images derived at different resolutions spanning orders of magnitude in length scales. A 38-mm-diameter carbonate core is studied in detail and imaged at low resolution—and at high resolution by taking four 5-mm-diameter subsets, one of which is imaged by use of full-length helical scanning. Fine-scale permeability transforms are derived by use of direct porosity/permeability relationships, random sampling of the porosity/permeability scatter plot as a function of porosity, and structural correlations combined with stochastic simulation. A range of these methods is applied at the coarse scale. We compare various upscaling methods, including renormalization theory, with direct solutions by use of a Laplace solver and report error bounds. Finally, we compare with experimental measurements of permeability at both the small-plug and the full-plug scale. We find that both numerically and experimentally for the carbonate sample considered, which displays nonconnecting vugs and intrafossil pores, permeability increases with scale. Although numerical and experimental results agree at the larger scale, the digital core-analysis results underestimate experimentally measured permeability at the smaller scale. Upscaling techniques that use basic averaging techniques fail to provide truthful vertical permeability at the fine scale because of large permeability contrasts. At this scale, the most accurate upscaling technique uses Darcy's law. At the coarse scale, an accurate permeability estimate with error bounds is feasible if spatial correlations are considered. All upscaling techniques work satisfactorily at this scale. A key part of the study is the establishment of porosity transforms between high-resolution and low-resolution images to arrive at a calibrated porosity map to constrain permeability estimates for the whole core.


1984 ◽  
Vol 28 ◽  
pp. 45-52 ◽  
Author(s):  
You-Zhao Bai ◽  
Sei Fukushima ◽  
Yohichi Gohshi

Various X-ray fluorescence spectrometers are now commercially available, and these spectrometers are classified into two categories, i.e., energy dispersive and wavelength dispersive (Table 1). Energy dispersive instruments are of low resolution. Wavelength dispersive instruments are often referred to as high resolution. However, commercially available wavelength dispersive instruments are usually equipped with a one-crystal dispersion unit. Therefore, to be more precise, these instruments could be called medium resolution apparatuses. There are other types of spectrometers which are two- or three-crysral spectrometers, and which are known to have very high resolving power. High resolution X-ray fluorescence spectrometers, however, have rarely been constructed. This is because this type of spectrometer needs a very precise and complicated scanning mechanism, and also because the intensity of X-ray fluorescence is often lost.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Stefan Stryker ◽  
Joel A. Greenberg ◽  
Shannon J. McCall ◽  
Anuj J. Kapadia

AbstractX-ray transmission imaging has been used in a variety of applications for high-resolution measurements based on shape and density. Similarly, X-ray diffraction (XRD) imaging has been used widely for molecular structure-based identification of materials. Combining these X-ray methods has the potential to provide high-resolution material identification, exceeding the capabilities of either modality alone. However, XRD imaging methods have been limited in application by their long measurement times and poor spatial resolution, which has generally precluded combined, rapid measurements of X-ray transmission and diffraction. In this work, we present a novel X-ray fan beam coded aperture transmission and diffraction imaging system, developed using commercially available components, for rapid and accurate non-destructive imaging of industrial and biomedical specimens. The imaging system uses a 160 kV Bremsstrahlung X-ray source while achieving a spatial resolution of ≈ 1 × 1 mm2 and a spectral accuracy of > 95% with only 15 s exposures per 150 mm fan beam slice. Applications of this technology are reported in geological imaging, pharmaceutical inspection, and medical diagnosis. The performance of the imaging system indicates improved material differentiation relative to transmission imaging alone at scan times suitable for a variety of industrial and biomedical applications.


Sign in / Sign up

Export Citation Format

Share Document