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Sources and Detectors

A detector must have adequate sensitivity to the radiation arriving j from the sample and monochromator over the entire spectral region L being considered. In addition, the source must be sufficiently intense j over both the wavenumber and transmittance range.  [Pg.24]

Sources of infrared emission have included the Globar, which is constructed of silicon carbide. There is also the Nernst filament, which is a mixture of oxides of zirconium, yttrium and erbium. However, a Nernst filament only conducts electricity- at elevated temperatures.  [Pg.24]

Most detectors consist of thermocouples of varying characteristics. [Pg.24]

FTlR spectrometers use a Globar or Nemst source for the mid-infrared region. If the far-infrared region is to be examined, then a high-pressure mercury lamp can be used. For the near-infrared, tungsten-halogen lamps are used as sources. [Pg.19]

There are two commonly used detectors employed for the mid-infrared region. The normal detector for routine use is a pyroelectric device incorporating deuterium tryglycine sulfate (DTGS) in a temperature-resistant alkali halide window. [Pg.19]

For more sensitive work, mercury cadmium telluride (MCT) can be used, but this has to be cooled to liquid nitrogen temperatures. In the far-infrared region, germanium or indium-antimony detectors are employed, operating at liquid helium temperatures. For the near-infrared region, the detectors used are generally lead sulfide photoconductors. [Pg.20]


To describe the X-ray imaging system the projection of 3D object points onto the 2D image plane, and nonlinear distortions inherent in the image detector system have to, be modelled. A parametric camera model based on a simple pinhole model to describe the projection in combination with a polynomal model of the nonlinear distortions is used to describe the X-ray imaging system. The parameters of the model are estimated using a two step approach. First the distortion parameters for fixed source and detector positions are calculated without any knowledge of the projection parameters. In a second step, the projection parameters are calculated for each image taken with the same source and detector positions but with different sample positions. [Pg.485]

Based on the camera model the distortion parameters are calculated for fixed source and detector positions without any knowledge of the projection parameters. [Pg.486]

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]

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]

Molecular Fluorescence A typical instrumental block diagram for molecular fluorescence is shown in Figure 10.45. In contrast to instruments for absorption spectroscopy, the optical paths for the source and detector are usually positioned at an angle of 90°. [Pg.427]

The source and detector of ultrasound in an ultrasound medical imager is called a transducer. The transducer is a piezoelectric crystal which physically changes its dimensions when a potential is appHed across the crystal (38). The appHcation of a force to the piezoelectric crystal which changes its dimensions creates a voltage in the crystal. AppHcation of an oscillating potential to the crystal causes the dimensions of the crystal to oscillate and hence create a sound at the frequency of the oscillation. The appHcation of an oscillating force to the crystal creates an alternating potential in the crystal. [Pg.52]

Instrumentation. The k region was developed usiag dispersive techniques adapted as appropriate from uv—vis spectroscopy. Unfortunately, k sources and detectors tend to be kiefficient compared to those for other spectral regions. [Pg.314]

For characterization purposes of bulk or thin-film semiconductors the features at Eq and E] are the most useflil. In a number of technologically important semiconductors (e.g., Hgi j d Te, and In Gai j ) the value of. ) is so small that it is not in a convenient spectral range for Modulation Spectroscopy, due to the limitations of light sources and detectors. In such cases the peak at E can be used. The features at Eq and are not useflil since they occur too far into the near-ultraviolet and are too broad. [Pg.388]

The device illustrates that important advantages can accrue from having x-ray source and detector near the sample, as they are here. [Pg.148]

Consider individual atoms of an element deposited on a thin substrate highly transparent to x-rays—say atoms of molybdenum upon paper. Let a characteristic line (say molybdenum K ) be excited by a polychromatic beam, x-ray source and detector both being located above the sample. So long as the number of molybdenum atoms is small, they will not noticeably attenuate the incident beam, nor will an x-ray quantum radiated by any molybdenum atom be absorbed by any other. Under these conditions, the intensity of the characteristic line will be proportional to the number of molybdenum atoms and hence to the thickness of the molybdenum film. [Pg.153]

The resolution of the ToF analyser is dependent upon the ability to measure the very small differences in time required for ions of a similar m/z to reach the detector. Increasing the distance that the ions travel between source and detector, i.e. increasing the length of the flight tube, would accentuate any such small time-differences. The implication of such an increase is that the instrument would be physically larger and this goes against the current trend towards the miniaturization of all analytical equipment. [Pg.62]

The analogue system simply corrects for the non-linearity of the source and detector. The reflectance analogue system, given as 7.8.29. on the next page. [Pg.429]

Fig. 3.19 Schematic illustration of the measurement geometry for Mossbauer spectrometers. In transmission geometry, the absorber (sample) is between the nuclear source of 14.4 keV y-rays (normally Co/Rh) and the detector. The peaks are negative features and the absorber should be thin with respect to absorption of the y-rays to minimize nonlinear effects. In emission (backscatter) Mossbauer spectroscopy, the radiation source and detector are on the same side of the sample. The peaks are positive features, corresponding to recoilless emission of 14.4 keV y-rays and conversion X-rays and electrons. For both measurement geometries Mossbauer spectra are counts per channel as a function of the Doppler velocity (normally in units of mm s relative to the mid-point of the spectrum of a-Fe in the case of Fe Mossbauer spectroscopy). MIMOS II operates in backscattering geometry circle), but the internal reference channel works in transmission mode... Fig. 3.19 Schematic illustration of the measurement geometry for Mossbauer spectrometers. In transmission geometry, the absorber (sample) is between the nuclear source of 14.4 keV y-rays (normally Co/Rh) and the detector. The peaks are negative features and the absorber should be thin with respect to absorption of the y-rays to minimize nonlinear effects. In emission (backscatter) Mossbauer spectroscopy, the radiation source and detector are on the same side of the sample. The peaks are positive features, corresponding to recoilless emission of 14.4 keV y-rays and conversion X-rays and electrons. For both measurement geometries Mossbauer spectra are counts per channel as a function of the Doppler velocity (normally in units of mm s relative to the mid-point of the spectrum of a-Fe in the case of Fe Mossbauer spectroscopy). MIMOS II operates in backscattering geometry circle), but the internal reference channel works in transmission mode...
The MIMOS II Mossbauer spectrometer sensor head (see Sect. 3.3) is located at the end of the /nstrument Deployment Device IDD (see Fig. 8.27) On Mars-Express Beagle-2, an European Space Agency (ESA) mission in 2003, the sensor head was also mounted on a robotic arm integrated to the Position Adjustable Workbench (PAW) instrument assembly [344, 345]. The sensor head shown in Figs. 8.28 and 8.29 carries the electromechanical transducer with the main and reference Co/Rh sources and detectors, a contact plate, and sensor. The contact plate and sensor are used in conjunction with the IDD to apply a small preload when it places the sensor head, holding it firmly against the target. [Pg.449]

Tables 6.27 and 6.31 show the main characteristics of ToF-MS. ToF-MS shows an optimum combination of resolution and sensitivity. ToF-MS instruments provide up to 40000 spectra s-1, a mass range exceeding 100000 (in principle unlimited), a resolution of 5000, and peak widths as short as 200 ms. This is better than quadruples and most ion traps can handle. Unlike the quadrupole-type instrument, the detector is detecting every introduced ion (high duty factor). This leads to a 20- to 100-times increase in sensitivity, compared to QMS used in scan mode. The mass range increases quadratically with the time range that is recorded. Only the ion source and detector impose the limits on the mass range. Mass accuracy in ToF-MS is sufficient to gain access to the elemental composition of a molecule. A single point is sufficient for the mass calibration of the instrument. ToF mass spectra are commonly calibrated using two known species, aluminium (27 Da) and coronene (300 Da). ToF is well established in combination with quite different ion sources like in SIMS, MALDI and ESI. Tables 6.27 and 6.31 show the main characteristics of ToF-MS. ToF-MS shows an optimum combination of resolution and sensitivity. ToF-MS instruments provide up to 40000 spectra s-1, a mass range exceeding 100000 (in principle unlimited), a resolution of 5000, and peak widths as short as 200 ms. This is better than quadruples and most ion traps can handle. Unlike the quadrupole-type instrument, the detector is detecting every introduced ion (high duty factor). This leads to a 20- to 100-times increase in sensitivity, compared to QMS used in scan mode. The mass range increases quadratically with the time range that is recorded. Only the ion source and detector impose the limits on the mass range. Mass accuracy in ToF-MS is sufficient to gain access to the elemental composition of a molecule. A single point is sufficient for the mass calibration of the instrument. ToF mass spectra are commonly calibrated using two known species, aluminium (27 Da) and coronene (300 Da). ToF is well established in combination with quite different ion sources like in SIMS, MALDI and ESI.
A survey spectrum covers a wide range of values of Eh, typically from OeV to 1000 eV or higher. The measured signals in Ekin would be converted to values of binding energy, and an ideal survey spectrum would appear as in Figure 2.4. Here it is assumed that the experiment is conducted with T— 0 K with an ideal source and detector, and furthermore that Heisenberg s uncertainty principle does not operate, the electrons have no spin and that all the electrons created leave the sample with no losses. [Pg.27]

In previous chapters it was shown that FRET can be reliably detected by donor fluorescence lifetime imaging. Here, we will focus on what is perhaps the most intuitive and straightforward way to record FRET imaging of sensitized emission (s.e., that is, the amount of acceptor emission that results from energy transferred by the donor through resonance) by filterFRET. While simple in principle, determinations of s.e. are complicated by overlap of excitation and emission spectra of the donors and acceptors, and by several imperfections of the recording optics, light sources and detectors. [Pg.301]

The preparation of a coated special fibre from a suitable material in a proper structure and the source and detector choice are not the final list of problems to be solved in the framework of sensor design. From Figure 3 it... [Pg.71]

A photonic realization of qubit can be obtained through the polarization state of a photon or usingthe continuous phase and amplitude of a many-photon laser beam [5,48]. At first, the difficulty in achieving significant photon-photon interactions necessary for multi-qubit operations can be seen as a drawback of this proposal. However, it was demonstrated that scalable QC is possible using only linear optical circuits and single-photon sources and detectors [16]. The method (known as the KLM scheme for Knill, Laflamme and Milburn) [49] uses quantum interference with auxiliary photons at a beam splitter as the source of interactions, and has... [Pg.191]


See other pages where Sources and Detectors is mentioned: [Pg.487]    [Pg.488]    [Pg.1125]    [Pg.2957]    [Pg.546]    [Pg.388]    [Pg.389]    [Pg.636]    [Pg.227]    [Pg.70]    [Pg.50]    [Pg.315]    [Pg.318]    [Pg.69]    [Pg.764]    [Pg.68]    [Pg.218]    [Pg.375]    [Pg.546]    [Pg.986]    [Pg.74]    [Pg.397]    [Pg.435]    [Pg.300]    [Pg.191]    [Pg.107]    [Pg.266]    [Pg.98]    [Pg.180]    [Pg.474]   


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Data collection on a conventional X-ray source with an area detector (including tabulated cases) and relationship to synchrotron radiation

Light sources and detectors for near-infrared analysers

Light sources and detectors for near-infrared analyzers

Light sources, filters and detectors

Performance with the Synchrotron Source and a Single-Element Detector

Practical Spectral Sources and Detectors for Analytical Spectrometry

Sources and detectors used in the mid-IR

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