Distribution function scattering

Smooth Surfaces Characterization of Sampie Bidirectionai Scattering Distribution Function... 

C.-H. Hung and C.-H. Tien, Modeling diffuse components by bidirectional scatter distribution function for... 

Figure 2 Scattering distribution function obtained with CSj solution (/PSH-PSO-PSH (a) 1%, (6) 20%, and (c) solid State (Reproduced by permission from Po/ymer, 1979, 20, 1181)...

Another statistical mechanical approach makes use of the radial distribution function g(r), which gives the probability of finding a molecule at a distance r from a given one. This function may be obtained experimentally from x-ray or neutron scattering on a liquid or from computer simulation or statistical mechanical theories for model potential energies [56]. Kirkwood and Buff [38] showed that for a given potential function, U(r)... 

Unlike the solid state, the liquid state cannot be characterized by a static description. In a liquid, bonds break and refomi continuously as a fiinction of time. The quantum states in the liquid are similar to those in amorphous solids in the sense that the system is also disordered. The liquid state can be quantified only by considering some ensemble averaging and using statistical measures. For example, consider an elemental liquid. Just as for amorphous solids, one can ask what is the distribution of atoms at a given distance from a reference atom on average, i.e. the radial distribution function or the pair correlation function can also be defined for a liquid. In scattering experiments on liquids, a structure factor is measured. The radial distribution fiinction, g r), is related to the stnicture factor, S q), by... 

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. 

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 ... 

In the field of Compton scattering the real space function it B(r) for the electron system is defined by the Fourier inversion of the distribution function of electron... 

Fig. 50. Small-angle neutron scattering results from different stars in a scaled form. The lines are the result of a fit with Eq. (94). Insert Related radial segment distribution functions obtained from a Fourier transformation of the theoretical scattering function. (Reprinted with permission from [150]. Copyright 1987 The American Physical Society, Maryland)...

Experimental considerations Frequently a numerical inverse Laplace transformation according to a regularization algorithm (CONTEST) suggested by Provencher [48,49] is employed to obtain G(T). In practice the determination of the distribution function G(T) is non-trivial, especially in the case of bimodal and M-modal distributions, and needs careful consideration [50]. Figure 10 shows an autocorrelation function for an aqueous polyelectrolyte solution of a low concentration (c = 0.005 g/L) at a scattering vector of q — 8.31 x 106 m-1 [44]. 

Mw = 2.1 x 106g/mol) in water, which is denoted Cw(t) in the original work [44]. The subscript indicates that both the incoming beam and the scattered light are vertically polarized. The correlation function was recorded for a solution with a concentration of c = 0.005 g/L at a scattering vector of q = 8.31 x 106m-1. The inset shows the distribution function of the relaxation times determined by an inverse Laplace transformation. 

Application in the Field of Scattering. Let us consider two important distribution functions, hc (x) and lu. (x). These functions shall describe the thicknesses of crystalline layers and the distances (long periods) between them, respectively. In this case we take into account polydispersity of the crystalline layers, if (at least) the two parameters dc and ac/dc are determined which are defined as the average thickness of the crystalline layers,... 

If the scattering entities in our material are stacks of layers with infinite lateral extension, Eq. (8.47) is applicable. This means that we can continue to investigate isotropic materials, and nevertheless unwrap the ID intensity of the layer stack. To this function Ruland applies the edge-enhancement principle of Merino and Tchoubar (cf. Sect. 8.5.3) and receives the interface distribution function (IDF), gi (x). Ruland discusses isotropic [66] and anisotropic [67] lamellar topologies. 

Stribeck N (1980) Computation of the Lamellar Nanostructure of Polymers by Computation and Analysis of the Interface Distribution Function from the Small-Angle X-ray Scattering. Ph.D. thesis, Phys. Chem. Dept., University of Marburg, Germany... 

The purpose of this section is to present direct evidence of nucleation during the induction period by means of synchrotron small angle X-ray scattering (SAXS). In the classical nucleation theory (CNT), the number density distribution function of nuclei of size N at time t, f(N, t), is expected to increase with an increase of t during the induction period and saturates to a steady f(N, t),fst(N) in the steady period. The change off(N, t) should correspond to that of the scattering intensity of SAXS. 

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