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From inversion method

Order and polydispersity are key parameters that characterize many self-assembled systems. However, accurate measurement of particle sizes in concentrated solution-phase systems, and determination of crystallinity for thin-film systems, remain problematic. While inverse methods such as scattering and diffraction provide measures of these properties, often the physical information derived from such data is ambiguous and model dependent. Hence development of improved theory and data analysis methods for extracting real-space information from inverse methods is a priority. [Pg.146]

In this section, we illustrate the application of the proposed inverse methods for OSD characterization, from observed Bscan images. [Pg.176]

This paper is structured as follows in section 2, we recall the statement of the forward problem. We remind the numerical model which relates the contrast function with the observed data. Then, we compare the measurements performed with the experimental probe with predictive data which come from the model. This comparison is used, firstly, to validate the forward problem. In section 4, the solution of the associated inverse problem is described through a Bayesian approach. We derive, in particular, an appropriate criteria which must be optimized in order to reconstruct simulated flaws. Some results of flaw reconstructions from simulated data are presented. These results confirm the capability of the inversion method. The section 5 ends with giving some tasks we have already thought of. [Pg.327]

In order to finally solve our inverse problem, we have to choose an adequate level of regularization. This section presents a few methods to select the value of p. Titterington et al. (1985) have made a comparison of the results obtained from different methods for choosing the value of the hyperparameters. [Pg.413]

Furthermore, the implementation of the Gauss-Newton method also incorporated the use of the pseudo-inverse method to avoid instabilities caused by the ill-conditioning of matrix A as discussed in Chapter 8. In reservoir simulation this may occur for example when a parameter zone is outside the drainage radius of a well and is therefore not observable from the well data. Most importantly, in order to realize substantial savings in computation time, the sequential computation of the sensitivity coefficients discussed in detail in Section 10.3.1 was implemented. Finally, the numerical integration procedure that was used was a fully implicit one to ensure stability and convergence over a wide range of parameter estimates. [Pg.372]

In order to obtain thin skinned, high flux membranes from PVA, several approaches were tried. The method presented in this article is reminiscent of the classical phase inversion method, which is widely applied in casting of asymmetric RO membranes. However, instead of using a gelling bath composed of a nonsolvent... [Pg.392]

We have reviewed here the implementation of the inverse method for going from densities to potentials, based on local-scaling transformations. For completeness, let us mention, however, that several other methods have also been advanced to deal with this inverse problem [101-111]. Consider the decomposition of into orbits Such orbits are characterized by the fact that... [Pg.220]

With this background infonnation on the inverse methods, it is instructive to examine the calculations for the inverse model in more detail. In Equation 5-23, the key to the model-building step is the inversion of the matrix CR ). This is a squire matrix with number of rows and columns equal to the number of measurement variables (nvars). From theory, a number of independent samples in the calibration set greater than or equal to nvars is needed in order to invert this matrix. For most analytical measurement systems, nvars (e.g., number of wavelengths) is greater than the number of independent samples and therefore RTr cannot be directly inverted. However, with a transformation, calculating she pseudo-inverse of R (R is possible. How this transformation is accomplished distinguishes the different inverse methods. [Pg.130]

Rommelaere, V., L. Arnaud, and J.-M. Barnola, Reconstructing Recent Atmospheric Trace Gas Concentrations from Polar Firn and Bubbly Ice Data by Inverse Methods, J. Geophys. Res., 102, 30069-30083 (1997). [Pg.840]

Notice that when we multiply eqn (4-3.10) by B-1 to produce eqn (4-3.11), as matrices do not necessarily commute, we must do so on the right-hand side of both sides of the equation. A method for finding the inverse of a non-singular matrix is given in Appendix A.4-2. From this method it is apparent why A-1 is only defined when det(A) = 0. [Pg.64]

Starch<—The inversion method described for flour (p. 63) is employed. From 5 to 10 grams of the substance are freed from fat by extraction with petroleum ether or other suitable solvent and from sugars (and dextrins) by treatment with 25% alcohol. The glucose found, multiplied by 0-9, gives the quantity of starch. [Pg.153]

The method applied to the calculation of the MWD from GPC- and PDC-measurements is formally the same it is based on the inversion of compact integral operators in the Hilbert space in a numerical way. Like the treatment of the problems connected with the analytical solution of the integrodifferential Eq. (41a b), also the treatment of this inversion method cannot be given here in all details it can be found in Ref. 8). Here, only an orientation in this universal and therefore somewhat abstract theory, stated by Greschner on the basis of a general superposition principle, will be given in a form specified for PDC and GPC, enabling easy application. [Pg.51]

This can well be seen from Fig. 24 showing three measured PDC-elution curves of the same standard anionic polystyrene PCC K-l 10000 (Pw = 1080) at 23 °C (very narrow), 17 °C (medium broad) and 15 °C (very broad). Only the very broad elution curve at 15 °C allows a simple caclulation of the MWD by means of the strip method S , because only 8% of the curve-width is caused by spreading and 92% by resolution (crD/cr = 0.08), whereas the inversion method G or K described above must be applied when the MWD is calculated from the elution curve 17 °C or even 23 °C, where 73 % of the curve-width is caused by spreading and only 27 %... [Pg.53]

Bernstein, R.B. and Zewail, A.H. (1990). From femtosecond temporal spectroscopy to the potential by a direct inversion method, Chem. Phys. Lett. 170, 321-328. [Pg.382]

Polymerisation. Emulsified droplets containing a monomer can react with a second monomer soluble in the continuous phase to form a membrane at the interface (i.e. diamine reacting with a acid dichloride). This is called interfacial polymerization. Many derivative methods can be set-up from this method, using pre-polymers in place of monomers, inversing the continuous and dispersed phases, developing a radical reaction. Covering all possible methods is not possible here. [Pg.31]

In the previous section, we have proposed the analytical method which can determine the adsorption free energy, j (or —AGa), based on the deformation polarizability, ao, and the dipole moment, n, of a molecule of solute, during the adsorption study on the solid surfaces as measured from inverse GC at infinite dilution. When the first value, i, of the adsorption free energy is equal to the energy measured at infinite dilution [i.e., the equilibrium concentration being extremely small, P = Pa in Eq. (95)], the pre-exponential factor of Henry s constant, K, can be obtained, depending on the experimental temperatures... [Pg.430]

A mixture of electrons, ions, and atoms forms a system similar to that which we considered in Chap. X, dealing with chemical equilibrium in gases. Equilibrium is determined, as it was there, by the mass action law. This law can be derived by balancing the rates of direct and inverse collisions, but it can also be derived from thermodynamics, and the equilibrium constant can be found from the heat of reaction and the chemical constants of the various particles concerned. The heats of reaction can be found from the various ionization potentials, quantities susceptible of independent measurement, and the chemical constants are determined essentially as in Chap. VIII. Thus there are no new principles involved in studying the equilibrium of atoms, electrons, and ions, and we shall merely give a qualitative discussion in this section, the statements being equivalent to mathematical results which can be established immediately from the methods of Chap. X. [Pg.334]

Liu C, Ball WP (1999) Application of inverse methods to contaminant source identification from aquitard diffusion profiles at Dover AFB. Delaware Water Resour Res 35 1975-1985... [Pg.95]

Crawley et. al. [57] applied the above equations to determine particle size distributions from turbidity measurements. The problems arise in finding a particle size distribution from the measured extinction coefficient due to the ill-defined inversion problem. Scholtz et.al. [58] focused on the problem of analyzing spectra of colloidal solutions, for which the size distribution was known from other methods like electron microscopy and light scattering they termed this transmission spectroscopy. ... [Pg.535]


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