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Photon fluxes

In traditional Fan-Beam CT the radiation emitted from the X-ray tube is collimated to a planar fan, and so most of the intensity is wasted in the collimator blades (Fig. 2a). Cone-Beam CT, where the X-rays not only diverge in the horizontal, but also in the vertical direction, allows to use nearly the whole emitted beam-profile and so makes best use of the available LINAC photon flux (Fig. 2b). So fast scanning of the samples three-dimensional structure is possible. For Cone-Beam 3D-reconstruction special algorithms, taking in consideration the vertical beam divergence of the rays, were developed. [Pg.493]

The absorption spectmm, 0(01), is the ratio of transition probability per unit time/incident photon flux. The incident photon flux is the number of photons per unit area per unit time passing a particular location, and is... [Pg.244]

Here t. is the intrinsic lifetime of tire excitation residing on molecule (i.e. tire fluorescence lifetime one would observe for tire isolated molecule), is tire pairwise energy transfer rate and F. is tire rate of excitation of tire molecule by the external source (tire photon flux multiplied by tire absorjDtion cross section). The master equation system (C3.4.4) allows one to calculate tire complete dynamics of energy migration between all molecules in an ensemble, but tire computation can become quite complicated if tire number of molecules is large. Moreover, it is commonly tire case that tire ensemble contains molecules of two, tliree or more spectral types, and experimentally it is practically impossible to distinguish tire contributions of individual molecules from each spectral pool. [Pg.3020]

Equations (C3.4.5) and (C3.4.6) cover the common case when all molecules are initially in their ground electronic state and able to accept excitation. The system is also assumed to be impinged upon by sources F. The latter are usually expressible as tlie product crfjo, where cr is an absorjition cross section, is tlie photon flux and ftois tlie population in tlie ground state. The common assumption is tliat Jo= q, i.e. practically all molecules are in tlie ground state because n n. This is tlie assumption of linear excitation, where tlie system exhibits a linear response to tlie excitation intensity. This assumption does not hold when tlie extent of excitation is significant, i.e. [Pg.3022]

Photons of energy hcv are generated initially in the cavity through spontaneous emission. Those that strike the cavity mirrors at 90° are retained within the cavity causing the photon flux to reach a level which is sufflciently high to cause stimulated emission to occur, and the active medium is said to lase. [Pg.339]

The transient current, derivable from equation 1, is given in equations 2 and 3 where T is the transit time and I is the absorbed photon flux. The parameter a can be further derived as equation 4 (4), where Tis the absolute temperature and is the distribution width (in units of kT) of a series of exponential traps. In this context, the carrier mobdity is governed by trapping and detrapping processes at these sites. [Pg.411]

There are important figures of merit (5) that describe the performance of a photodetector. These are responsivity, noise, noise equivalent power, detectivity, and response time (2,6). However, there are several related parameters of measurement, eg, temperature of operation, bias power, spectral response, background photon flux, noise spectra, impedance, and linearity. Operational concerns include detector-element size, uniformity of response, array density, reflabiUty, cooling time, radiation tolerance, vibration and shock resistance, shelf life, availabiUty of arrays, and cost. [Pg.420]

Fig. 2. Blackbody radiated photon flux interval distribution from ambient temperature up to 2000 K. Ambient objects do not have detectable flux for... Fig. 2. Blackbody radiated photon flux interval distribution from ambient temperature up to 2000 K. Ambient objects do not have detectable flux for...
When equation 12 is vaUd, the detector is said to be a background-limited infrared photodetector (BLIP). When this is the case, attempts often are made to improve D by cold shielding which reduces ( ). The ideal D is shown in Figure 3 as a function of wavelength with background photon flux as a parameter. The line of termination in the lower left corner represents TN values for a 180° (27T) detector field of view, 300 K ambient background... [Pg.422]

The responsivity and g-r noise may be analyzed to obtain background photon flux and temperature dependence of responsivity, noise, and detectivity. Typically, n > p, and both ate determined by shallow impurity levels. The minority carrier density is the sum of thermal and optical contributions. [Pg.434]

The large variability in elemental ion yields which is typical of the single-laser LIMS technique, has motivated the development of alternative techniques, that are collectively labeled post-ablation ionization (PAI) techniques. These variants of LIMS are characterized by the use of a second laser to ionize the neutral species removed (ablated) from the sample surface by the primary (ablating) laser. One PAI technique uses a high-power, frequency-quadrupled Nd-YAG laser (A, = 266 nm) to produce elemental ions from the ablated neutrals, through nonresonant multiphoton ionization (NRMPI). Because of the high photon flux available, 100% ionization efflciency can be achieved for most elements, and this reduces the differences in elemental ion yields that are typical of single-laser LIMS. A typical analytical application is discussed below. [Pg.588]

To protect the sample from stray electrons from the anode, from heating effects, and from possible contamination by the source enclosure, a thin (-2 pm) window of aluminum foil is interposed between the anode and the sample. For optimum X-ray photon flux on the surface (i. e. optimum sensitivity), the anode must be brought as close to the sample as possible, which means in practice a distance of -2 cm. The entire X-ray source is therefore retractable via a bellows and a screw mechanism. [Pg.11]

Depends markedly on purity, temperature and photon flux resistivity of liquid Se at 400° is 1.3 x lO ohmcm. [Pg.754]

In a steady state experiment the PIA signal Y is proportional to neq. Measuring the PIA with a lock-in amplifier means exciting the sample with a periodic time-dependent pump photon flux. The latter can be approximated by a square wave that switches between a constant flux and zero photons with a frequency /= 1/r. As shown in Refs. [32] and [33] the PIA signal, measured with a lock-in amplifier Y, shows the same functional dependence on p as ncq in Eq. (9.5). For the monomo-lecular (p-1) and bimolecular (//=2) case the influence of r depends on t, the lifetime of the observed states, as follows ... [Pg.153]

Figure 19. PMC potential and photocurrent-potential curves for an Si-MOS device (2 nm Si02) at different photon flux densities (indicated for photocurrents). Figure 19. PMC potential and photocurrent-potential curves for an Si-MOS device (2 nm Si02) at different photon flux densities (indicated for photocurrents).
Sodium Guide Star Brightness. From the properties of the Na atom and the Na layer (Table 1), we can estimate the power needed for the AO system. Assuming isotropic emission and no saturation, the photon flux F of the LGS observed with the WFS is given by ... [Pg.220]

It should be noted that when we compare the brightness of a LGS to a NGS, the result depends on the spectral bandwidth, because the LGS is a line source, whereas the NGS is a continuum one. The magnitude scale is a logarithmic measure of flux per spectral interval (see Ch. 15). This means that a (flat) continuum source has a fixed magnitude, no matter how wide the filter is. In contrast, the magnitude of a line source is smaller for narrower bandpasses. It is therefore advisable to use the equivalent magnitude only for qualitative arguments. The photon flux should be used in careful system analyses. [Pg.220]

Fig. 1. Rates of CO2 assimilation, A (/miol s ) leaf conductance, g (mol m s ) intercellular partial pressure of CO2, Pi (Pa) soil water potential and leaf water potential, xp (MPa) during gas-exchange measurements of a 30-day-old cotton plant, plotted against day after watering was withheld. Measurements were made with 2 mmol m sec" photon flux density, 30 °C leaf temperature, and 2.0 kPa vapour pressure difference between leaf and air (S.C. Wong, unpublished data). Fig. 1. Rates of CO2 assimilation, A (/miol s ) leaf conductance, g (mol m s ) intercellular partial pressure of CO2, Pi (Pa) soil water potential and leaf water potential, xp (MPa) during gas-exchange measurements of a 30-day-old cotton plant, plotted against day after watering was withheld. Measurements were made with 2 mmol m sec" photon flux density, 30 °C leaf temperature, and 2.0 kPa vapour pressure difference between leaf and air (S.C. Wong, unpublished data).
Fig. 2. Rates of CO2 assimilation,. 4, and leaf conductances, g, as functions of intercellular partial pressure of CO2, p in Zea mays on various days after withholding watering. Measurements made with 9.5,19.0,30.5, and 38.0 Pa ambient partial pressure of CO2, 2 mmol m" s" photon flux density, 30 °C leaf temperature, and 2.0 kPa vapour pressure differences between leaf and air. Closed symbols represent measurements with 30.5 Pa ambient partial pressure of COj. Leaf water potentials were 0.05, - 0.2, - 0.5 and - 0.8 MPa on day 0, 4, 11 and 14, respectively (after Wong et al., 1985). Fig. 2. Rates of CO2 assimilation,. 4, and leaf conductances, g, as functions of intercellular partial pressure of CO2, p in Zea mays on various days after withholding watering. Measurements made with 9.5,19.0,30.5, and 38.0 Pa ambient partial pressure of CO2, 2 mmol m" s" photon flux density, 30 °C leaf temperature, and 2.0 kPa vapour pressure differences between leaf and air. Closed symbols represent measurements with 30.5 Pa ambient partial pressure of COj. Leaf water potentials were 0.05, - 0.2, - 0.5 and - 0.8 MPa on day 0, 4, 11 and 14, respectively (after Wong et al., 1985).
Since the sensitizer Rose Bengal is recyclable, relatively high concentrations (5 10 M) can be used without raising cost issues and optical detection problems [21]. Under these conditions, it was shovm that molecules at any position in the micro channel have a similar photon flux. [Pg.645]


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