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Identification Imaging

The major drawback of this identification method, as used to date, is that only a part of the useful information contained into original Bscan image, i.e. segmented Bscan image, is used for defect characterization. Moreover, it requires the availability of defect classification information (i.e. if the defect is volumetric or planar, e.g. a crack or a lack of fusion), which, generally, may be as difficult to obtain as the defect parameters themselves. Therefore, we... [Pg.171]

In many cases, the methods used to solve identification problems are based on an iterative minimization of some performance criterion measuring the dissimilarity between the experimental and the synthetic data (generated by the current estimate of the direct model). In our case, direct quantitative comparison of two Bscan images at the pixels level is a very difficult task and involves the solution of a very difficult optimization problem, which can be also ill-behaved. Moreover, it would lead to a tremendous amount of computational burden. Segmented Bscan images may be used as concentrated representations of the useful... [Pg.172]

Allows the identification of the different objects present in the segmented image. Different approaches are used for the recognition ... [Pg.180]

Microscopy is an unusual scientific discipline, involving as it does a wide variety of microscopes and techniques. All have in common the abiUty to image and enlarge tiny objects to macroscopic size for study, comparison, evaluation, and identification. Few industries or research laboratories can afford to ignore microscopy, although each may use only a small fraction of the various types. Microscopy review articles appear every two years m. Jinalytical Chemistty (1,2). Whereas the style of the Enclyclopedia employs lower case abbreviations for analytical techniques and instmments, eg, sem for scanning electron microscope, in this article capital letters will be used, eg, SEM. [Pg.328]

The major STEM analysis modes are the imaging, diffraction, and microanalysis modes described above. Indeed, this instrument may be considered a miniature analytical chemistry laboratory inside an electron microscope. Specimens of unknown crystal structure and composition usually require a combination of two or more analysis modes for complete identification. [Pg.167]

Monnier, O., Fevotte, G., Hoff, C. and Klein, J.P., 1997. Model identification of batch cooling crystallizations through calorimetry and image analysis. Chemical Engineering Science, 52, 1125-1139. [Pg.315]

Nuclear magnetic resonance (NMR) is the principal technique for the identification of organic compounds and is among the leading techniques for the determination of their structures. The technique has also been developed, as magnetic resonance imaging (MRI), as a diagnostic procedure in medicine. [Pg.904]

In 1994, we proposed that a metallic needle having a nano-tip at its apex be employed as a nano-light-source for microscopy attaining nanometric spatial resolution [2]. Later, we expanded the technique to Raman spectroscopy for molecular nano-identification, nano-analysis and nano-imaging. In this chapter, we give a brief introduction to local plasmons and microscopy using a metallic nano-needle to produce the local plasmons. Then, we describe the microscope that we built and... [Pg.19]

A nano-light-source generated on the metallic nano-tip induces a variety of optical phenomena in a nano-volume. Hence, nano-analysis, nano-identification and nanoimaging are achieved by combining the near-field technique with many kinds of spectroscopy. The use of a metallic nano-tip applied to nanoscale spectroscopy, for example, Raman spectroscopy [9], two-photon fluorescence spectroscopy [13] and infrared absorption spectroscopy [14], was reported in 1999. We have incorporated Raman spectroscopy with tip-enhanced near-field microscopy for the direct observation of molecules. In this section, we will give a brief introduction to Raman spectroscopy and demonstrate our experimental nano-Raman spectroscopy and imaging results. Furthermore, we will describe the improvement of spatial resolution... [Pg.24]

As the reader might have noticed, many conclusions in electrocatalysis are based on results obtained with electrochemical techniques. In situ characterization of nanoparticles with imaging and spectroscopic methods, which is performed in a number of laboratories, is invaluable for the understanding of PSEs. Identification of the types of adsorption sites on supported metal nanoparticles, as well as determination of the influence of particle size on the adsorption isotherms for oxygen, hydrogen, and anions, are required for further understanding of the fundamentals of electrocatalysis. [Pg.551]

Fig. 5.2.3 Identification of rivulets and surface wetting in a packing of 5-mm diameter glass spheres contained within a column of inner diameter 40 mm. The data were acquired in a 3D array with an isotropic voxel resolution of 328 xm x 328 pm x 328 [im. (a) The original image of trickle flow is first binary gated, so that only the liquid distribution within the image is seen (white) gas-filled pixels and pixels containing glass spheres show up as zero intensity (black), (b) The liquid distribu-... Fig. 5.2.3 Identification of rivulets and surface wetting in a packing of 5-mm diameter glass spheres contained within a column of inner diameter 40 mm. The data were acquired in a 3D array with an isotropic voxel resolution of 328 xm x 328 pm x 328 [im. (a) The original image of trickle flow is first binary gated, so that only the liquid distribution within the image is seen (white) gas-filled pixels and pixels containing glass spheres show up as zero intensity (black), (b) The liquid distribu-...
Fig. 5.2.7 Identification of location and size of local pulses within the trickle bed. A high spatial resolution image (in-plane spatial resolution 1 75 [tm x 175 im slice thickness 1 mm) is overlayed with a standard deviation map calculated from images acquired at a spatial resolution of in-plane spatial resolution 1.4 mm x 2.8 mm slice thickness 2 mm. Fig. 5.2.7 Identification of location and size of local pulses within the trickle bed. A high spatial resolution image (in-plane spatial resolution 1 75 [tm x 175 im slice thickness 1 mm) is overlayed with a standard deviation map calculated from images acquired at a spatial resolution of in-plane spatial resolution 1.4 mm x 2.8 mm slice thickness 2 mm.
Stress myocardial perfusion imaging with the radionuclides technetium-99m sestamibi or thallium-201 allows for the identification of multivessel disease and assessment of myocardial viability. [Pg.68]


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See also in sourсe #XX -- [ Pg.132 , Pg.140 ]




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Identification digital imaging

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