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Resolution of detector

X-ray topography is the X-ray analogue of transmission election microscopy and as such provides a map of the strain distribution in a crystal. The theory of image formation is well established and image simulation is thus a powerful means of defect identification. Despite a reputation for being a slow and exacting technique, with modem detector technology and care to match spatial resolution of detector and experiment, it can be a powerful and economical quality-control tool for the semiconductor industry. [Pg.215]

Energy Resolution of Detector Will the detector measure the energy of the radiation striking it, and if so, how precisely does it do this If two y rays of energies 1.10 and 1.15 MeV strike the detector, can it distinguish between them ... [Pg.538]

Time Resolution of Detector or Its Pulse-Resolving Time How high a counting rate will be measured by the detector without error How accurately and precisely can one measure the time of arrival of a particle at the detector ... [Pg.538]

Vibration of equipment in contact with the cryostat. This was the reason for the loss of resolution of detectors fitted with first generation electrically cooled cryostats. (See Section 3.7.5). [Pg.50]

Already in 1972, Magde, Webb, and Elson published the first paper on fluorescence correlation spectroscopy yielding chemical rate constants and diffusion coefficients [2], followed by a series of further reports on these novel techniques [3-5]. However, several further developments were necessary for FCS to reach its current power which has been reviewed several times as for example in [6-10]. One key step in the evolution of FCS was its combination with confocal microscopy to enhance spatial resolution basically down to the diffraction limit of the fluorescence light and the concomitant increase in sensitivity [11]. Further important technical improvements concern the quality of optical components and the sensitivity and time resolution of detectors. Additionally, better labels and labeling strategies have become available, a point which should not be underestimated. [Pg.257]

It is shown how phase contrast X-ray microtomography can be realised with a (commercial) polychromatic X-ray microfocus tomograph provided the source size and the resolution of the detector are sufficiently small and the distance between source and detector is sufficiently large. The technique opens perspectives for high resolution tomography of light objects... [Pg.573]

For this experiment, as well as for the microtomography ( 3.2) we used the commercial desktop microtomography system Skyscan 1072 [5], the setup of which is sketched in Figure 1. For this instrument, which is designed to study relatively large objects with a diameter up to 50 mm, the source size is 8 pm, the distance source-detector is about 50 cm and the effective resolution of the detector is about 80 pm. For this system and this object, the global effective resolution a is estimated to be of the order of 50 to 100 pm [6]. [Pg.576]

The University developed a method of determination of the material residual strength, based on measurement of the change of phase velocity of ultrasonic waves, as well as an ultrasonic flaw detector-tomograph with multi-element transducers of the type of phased acoustic array. It enables control of the internal structure of materials and products of up to 300 mm thickness, with the resolution of up to 0.5 mm. In the same university, work on NDT is also carried out in the welding and electro-acoustic departments. [Pg.970]

In the simplest fomi, reflects the time of flight of the ions from the ion source to the detector. This time is proportional to the square root of the mass, i.e., as the masses of the ions increase, they become closer together in flight time. This is a limiting parameter when considering the mass resolution of the TOP instrument. [Pg.1351]

The ability to identify different mass species depends on the energy resolution of the detector which is typically 15 keV fiill width at half maximum (FWFIM). For example, silver has a mass M2 = 108 and tin has a mass A , = 119. The difference between . = 0.862 and = 0.874 is 0.012. For 2 MeV helium ions the... [Pg.1831]

Direct time-dependent detection is limited by the response time of detectors, which depends on the frequency range, and the electronics used for data acquisition. In the most favourable cases, modem detector/oscilloscope combinations achieve a time resolution of up to 100 ps, but 1 ns is more typical. Again, this reaction has been of fiindamental theoretical interest for a long time [59, 60]. [Pg.2126]

Infrared instruments using a monochromator for wavelength selection are constructed using double-beam optics similar to that shown in Figure 10.26. Doublebeam optics are preferred over single-beam optics because the sources and detectors for infrared radiation are less stable than that for UV/Vis radiation. In addition, it is easier to correct for the absorption of infrared radiation by atmospheric CO2 and 1420 vapor when using double-beam optics. Resolutions of 1-3 cm are typical for most instruments. [Pg.393]

Since the microchannel plate collector records the arrival times of all ions, the resolution depends on the resolution of the TOP instrument and on the response time of the microchannel plate. A microchannel plate with a pore size of 10 pm or less has a very fast response time of less than 2 nsec. The TOP instrument with microchannel plate detector is capable of unit mass resolution beyond m/z 3000. [Pg.198]

Quadmpole mass spectrometers (mass filters) allow ions at each m/z value to pass through the analyzer sequentially. For example, ions at m/z 100, 101, and 102 are allowed to pass one after the other through the quadmpole assembly so that first m/z 100 is transmitted, then m/z 101, then m/z 102, and so on. Therefore, the ion collector at the end of the quadmpole unit needs to cover only one point or focus in space and can be placed immediately behind the analyzer (Figure 30.1). A complete mass spectram is recorded over a period of time (temporally), which is set by the voltages on the quadmpole analyzer. In this mode of operation, the ions are said to be scanned sequentially. The resolution of m/z values is dependent solely on the analyzer and not on the detector. The single-point collector is discussed in detail in Chapter 28. [Pg.211]

By use of an electrostatic ion mirror called a reflectron, arrival times of ions of the same m/z value at the detector can be made more nearly equal. The reflectron improves resolution of m/z values. [Pg.406]

The NEP may be written in terms of the detector element active area, the number of detector pixels elements cormected for additive output the electronic noise bandwidth B and the detector element detectivity, D. Typically = 1, but may be increased for improved sensitivity with an attendant loss in resolution. [Pg.291]


See other pages where Resolution of detector is mentioned: [Pg.322]    [Pg.307]    [Pg.152]    [Pg.215]    [Pg.11]    [Pg.181]    [Pg.1144]    [Pg.322]    [Pg.307]    [Pg.152]    [Pg.215]    [Pg.11]    [Pg.181]    [Pg.1144]    [Pg.401]    [Pg.595]    [Pg.1174]    [Pg.1234]    [Pg.1235]    [Pg.1236]    [Pg.1353]    [Pg.1424]    [Pg.1426]    [Pg.1624]    [Pg.1632]    [Pg.1806]    [Pg.1808]    [Pg.1830]    [Pg.1832]    [Pg.1833]    [Pg.2084]    [Pg.2485]    [Pg.166]    [Pg.166]    [Pg.171]    [Pg.172]    [Pg.191]    [Pg.252]    [Pg.290]    [Pg.482]    [Pg.132]   
See also in sourсe #XX -- [ Pg.41 ]

See also in sourсe #XX -- [ Pg.73 ]




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