Reasonable spatial resolution

Another issue of concern is the amplitude of magnetic field gradients required for solids imaging. For spectra up to a few kHz wide, standard frequency encoding schemes can be used to obtain reasonable spatial resolution. This will not work for broader lines, but it is well known that phase encoding is much more tolerant to line broadening and can be used for spectral widths in excess of 100 kHz with no major loss in spatial resolution. 

Reasonable spatial resolution (> 500 x 500 pixels with a clean Point Spread Function). 

How can a reasonable spatial resolution still be obtained when unaging in the microwave region (radar, radio astronomy) ... 

Radioactive aerosols are frequently used in deposition or medical application studies because they allow noninvasive measurements of high sensitivity and reasonable spatial resolution. The fraction of aerosols deposited in the body is derived from radioactivity balance considerations. 

Other limitation for the spatial resolution can be found in the detector. A limited number of pixels in the camera array can be a reason for pure resolution in the case of a big field of view. For example, if field of view should be 10 by 10 nun with camera division 512x512 pixels the pixel size will be approximately 20 microns. To improve the relation of the field of view and the spatial resolution a mega-pixel sensor can be used. One more limitation for the spatial resolution is in mechanical movement (rotation) of the object, camera and source. In the case of a mechanical movement all displacements and rotations should be done with accuracy better than the spatial resolution in any tested place of the object. In the case of big-size assemblies and PCB s it is difficult to avoid vibrations, axle play and object non-planarity during testing. 

The thrust of development is toward ever better spatial resolution, which means the smallest possible spot size on the sample compatible with adequate signal-to-noise ratio, for acquisition within a reasonable length of time. 

The results show that at 2 torr, ku = 2.5 X 10 8 and at 760 torr ku = 1.0 X 10 8 cm.3 molecule-1 sec.-1 This is reasonably good agreement in view of the possible errors. Furthermore, the values of ku obtained are consistent with earlier estimates based on comparisons with similar reactions (10, 19). Our purpose in presenting it here is to illustrate the potential use of flames in estimating more accurate rate constants for reactions like Reaction 14. Of course, the influence of diffusion must always be accounted for in such estimations diffusion is particularly important at low pressures and for small ion concentrations. (It is often advantageous to work at low pressures because the spatial resolution is much better than at 1 atm. At low pressures most measurements are made in or close to the reaction zone itself. At high pressures, where the reaction zone is thinner, measurements are made both in the reaction zone and in the burned gases.)... 

Although ASL has been performed in the acute stroke setting, this currently is seldom done, for several reasons. Current ASL pulse sequences are somewhat more time consuming than DSC, requiring 6 minutes in the study cited above, compared to approximately 1 minute for DSC or CTP. ASL perfusion maps are far noisier than DSC maps, and have less spatial resolution. 

There are two principal sources of reliable partitioning data for any trace element glassy volcanic rocks and high temperature experiments. For the reasons outlined above, both sources rely on analytical techniques with high spatial resolution. Typically these are microbeam techniques, such as electron-microprobe (EMPA), laser ablation ICP-MS, ion-microprobe secondary ion mass spectrometry (SIMS) or proton-induced X-ray emission (PIXE). 

In general, XPS is the preferred technique for studying oxidation states and ligand effects. However, there is a good reason why one should be interested in deriving chemical information from AES whereas the spatial resolution of XPS is at best a few micrometers, Auger spectra can be obtained from spots with diameters as small as a few nanometers. It would be extremely interesting to have oxidation state information on the same scale as well ... 

Although this technique is not normally used for thin polymer films for the reasons described before, it can be used for analyzing the surface of polymer composites containing conductive fillers, e.g. carbon fibers. In addition, because of the surface specificity, the sampled area can be maintained almost identically to the beam cross-section so that the scanning Auger microscope (SAM) can have a spatial resolution that is much better than that of microprobe analysis. 

In conventional gas electron diffraction experiments, an effusive beam is used in which vibrational levels of molecules are thermally populated and the width of a peak in a radial distribution curve is determined by thermally averaged mean amplitudes. When a molecular beam or a free jet is used, mean amplitudes could become small, since the contribution from the vibrationally excited levels is reduced significantly. As a consequence, sharper peaks are expected in the radial distribution curve, and the spatial resolution of the snapshot could be improved. However, it seems that the observed peaks in the radial distribution curve are considerably broad even though a molecular beam is used. There could be some reasons to have such broadened peaks in the radial distribution curve. 

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