Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Fourier transform distributions

The light diffracted, in a far field approximation, follows the Fourier transform distribution and the intensity for the different diffraction orders, m, is proportional to sim 2(diffraction orders is given by XR/d, where R is the distance between the binary transmissive diffraction grating and the Fourier plane (Kashnow, 1973). [Pg.258]

Fig. 2. Distribution of sdicon centers in soluble sdicate solutions from Si Fourier-transform nmr spectroscopy (7,37), where (—) represents (--------),... Fig. 2. Distribution of sdicon centers in soluble sdicate solutions from Si Fourier-transform nmr spectroscopy (7,37), where (—) represents (--------),...
The Fourier transform of the EXAFS of Figure 5 is shown in Figure 6 as the solid curve It has two large peaks at 2.38 and 2.78 A as well as two small ones at 4.04 and 4.77 A. In this example, each peak is due to Mo—Mo backscattering. The peak positions are in excellent correspondence with the crystallographically determined radial distribution for molybdenum metal foil (bcc)— with Mo—Mo interatomic distances of2.725, 3.147, 4.450, and 5.218 A, respectively. The Fourier transform peaks are phase shifted by -0.39 A from the true distances. [Pg.221]

Obviously, the theory outhned above can be applied to two- and three-dimensional systems. In the case of a two-dimensional system the Fourier transforms of the two-particle function coefficients are carried out by using an algorithm, developed by Lado [85], that preserves orthogonality. A monolayer of adsorbed colloidal particles, having a continuous distribution of diameters, has been investigated by Lado. Specific calculations have been carried out for the system with the Schulz distribution [86]... [Pg.156]

The real space pair distributions gy(rj is the inverse Fourier transform of (Sy(Q)-l), that is ... [Pg.128]

Where, /(k) is the sum over N back-scattering atoms i, where fi is the scattering amplitude term characteristic of the atom, cT is the Debye-Waller factor associated with the vibration of the atoms, r is the distance from the absorbing atom, X is the mean free path of the photoelectron, and is the phase shift of the spherical wave as it scatters from the back-scattering atoms. By talcing the Fourier transform of the amplitude of the fine structure (that is, X( )> real-space radial distribution function of the back-scattering atoms around the absorbing atom is produced. [Pg.140]

It can be shown that the right-hand side of Eq. (3-208) is the -dimensional characteristic function of a -dimensional distribution function, and that the -dimensional distribution function of afn, , s n approaches this distribution function. Under suitable additional hypothesis, it can also be shown that the joint probability density function of s , , sjn approaches the joint probability density function whose characteristic function is given by the right-hand side of Eq. (3-208). To preserve the analogy with the one-dimensional case, this distribution (density) function is called the -dimensional, zero mean gaussian distribution (density) function. The explicit form of this density function can be obtained by taking the i-dimensional Fourier transform of e HsA, with the result.45... [Pg.160]

Keilson-Storer kernel 17-19 Fourier transform 18 Gaussian distribution 18 impact theory 102. /-diffusion model 199 non-adiabatic relaxation 19-23 parameter T 22, 48 Q-branch band shape 116-22 Keilson-Storer model definition of kernel 201 general kinetic equation 118 one-dimensional 15 weak collision limit 108 kinetic equations 128 appendix 273-4 Markovian simplification 96 Kubo, spectral narrowing 152... [Pg.297]

We are now ready to derive an expression for the intensity pattern observed with the Young s interferometer. The correlation term is replaced by the complex coherence factor transported to the interferometer from the source, and which contains the baseline B = xi — X2. Exactly this term quantifies the contrast of the interference fringes. Upon closer inspection it becomes apparent that the complex coherence factor contains the two-dimensional Fourier transform of the apparent source distribution I(1 ) taken at a spatial frequency s = B/A (with units line pairs per radian ). The notion that the fringe contrast in an interferometer is determined by the Fourier transform of the source intensity distribution is the essence of the theorem of van Cittert - Zemike. [Pg.281]

The fundamental quantity for interferometry is the source s visibility function. The spatial coherence properties of the source is connected with the two-dimensional Fourier transform of the spatial intensity distribution on the ce-setial sphere by virtue of the van Cittert - Zemike theorem. The measured fringe contrast is given by the source s visibility at a spatial frequency B/X, measured in units line pairs per radian. The temporal coherence properties is determined by the spectral distribution of the detected radiation. The measured fringe contrast therefore also depends on the spectral properties of the source and the instrument. [Pg.282]

The roughness can also be measured from the Fourier transform x of the distribution x ... [Pg.411]

Surface forces measurement is a unique tool for surface characterization. It can directly monitor the distance (D) dependence of surface properties, which is difficult to obtain by other techniques. One of the simplest examples is the case of the electric double-layer force. The repulsion observed between charged surfaces describes the counterion distribution in the vicinity of surfaces and is known as the electric double-layer force (repulsion). In a similar manner, we should be able to study various, more complex surface phenomena and obtain new insight into them. Indeed, based on observation by surface forces measurement and Fourier transform infrared (FTIR) spectroscopy, we have found the formation of a novel molecular architecture, an alcohol macrocluster, at the solid-liquid interface. [Pg.3]

In general, the topology of interprocessor communication reflects both the structure of the mathematical algorithms being employed and the way that the wave packet is distributed. For example, our very first implementation of parallel algorithms in a study of planar OH - - CO [47] used fast Fourier transforms (FFTs) to compute the action of 7, which also required all-to-all communication but in a topology that is very different from the simple ring-like structure shown in Fig. 5. [Pg.29]

Figure 5. The Fourier transformed signal AS[r, i] of I2/CCI4. The pump-probe delay times are I = 200 ps, 1 ns, and 1 ps. The green bars indicate the bond lengths of iodine in the X and A/A states. The blue bars show the positions of the first two intermolecular peaks in the pair distribution function gci-ci- (See color insert.)... Figure 5. The Fourier transformed signal AS[r, i] of I2/CCI4. The pump-probe delay times are I = 200 ps, 1 ns, and 1 ps. The green bars indicate the bond lengths of iodine in the X and A/A states. The blue bars show the positions of the first two intermolecular peaks in the pair distribution function gci-ci- (See color insert.)...
Figure 6. The Fourier transformed signal AS[r, i] of CH2I2/CH3OH. The pump-probe time delays vary between i = —250 ps and 1 ps. The pair distribution function gl-I peaks in the 3 A region. If T < 50 ns, the I—I bond corresponds to the short-lived intermediate (CH2ri), and if x > 100 ns it belongs to the (I3") ion. Red curves indicate the theory, and black curves describe the experiment. Figure 6. The Fourier transformed signal AS[r, i] of CH2I2/CH3OH. The pump-probe time delays vary between i = —250 ps and 1 ps. The pair distribution function gl-I peaks in the 3 A region. If T < 50 ns, the I—I bond corresponds to the short-lived intermediate (CH2ri), and if x > 100 ns it belongs to the (I3") ion. Red curves indicate the theory, and black curves describe the experiment.
The essence of analyzing an EXAFS spectrum is to recognize all sine contributions in x(k)- The obvious mathematical tool with which to achieve this is Fourier analysis. The argument of each sine contribution in Eq. (8) depends on k (which is known), on r (to be determined), and on the phase shift

characteristic property of the scattering atom in a certain environment, and is best derived from the EXAFS spectrum of a reference compound for which all distances are known. The EXAFS information becomes accessible, if we convert it into a radial distribution function, 0 (r), by means of Fourier transformation ... [Pg.141]

The reciprocal form factor [22] is the Fourier transform of the momentum distribution,... [Pg.131]

The Fourier transform is distributive over summation, which means that the Fourier transform of the two individual signals is equal to the sum of the Fourier transforms of the two individual signals +f2(t)] = F /j(t)] -i- Flfjit)]. [Pg.529]


See other pages where Fourier transform distributions is mentioned: [Pg.399]    [Pg.121]    [Pg.399]    [Pg.121]    [Pg.464]    [Pg.42]    [Pg.352]    [Pg.233]    [Pg.1827]    [Pg.220]    [Pg.589]    [Pg.18]    [Pg.294]    [Pg.85]    [Pg.281]    [Pg.143]    [Pg.140]    [Pg.134]    [Pg.529]    [Pg.14]    [Pg.9]    [Pg.9]    [Pg.15]    [Pg.22]    [Pg.164]    [Pg.164]    [Pg.560]    [Pg.323]    [Pg.397]   
See also in sourсe #XX -- [ Pg.261 , Pg.262 , Pg.263 ]




SEARCH



Fourier transform distance distributions

Gaussian charge distribution, Fourier transform

Gaussian distribution Fourier transform

© 2024 chempedia.info