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Determinant and inverse

In this section, we develop some useful relationships involving the determinants and inverses of projected tensors. Let S ap be the Riemannian representation of an arbitrary symmetric covariant tensor with a Cartesian representation S v We may write the Riemannian representation in block matrix form, using the indices a,b to denote blocks in which a or p mns over the soft coordinates and i,j to represent hard coordinates, as... [Pg.171]

The parameter estimates are then obtained by maximising either Eqs. (5.88) or (5.89). The result given by Eq. (5.89) is called the exact log-likelihood function. However, when dealing with a long time series with many data points, it will be computationally expensive to compute the determinant and inverse required by the exact log-likelihood function at every iteration. Instead, the exact probability can be... [Pg.246]

First determine what parameters will be used for describing bond lengths and angles. Then determine torsional, inversion, and nonbonded interaction parameters. [Pg.241]

This important equation shows that the stationary-state free-radical concentration increases with and varies directly with and inversely with. The concentration of free radicals determines the rate at which polymer forms and the eventual molecular weight of the polymer, since each radical is a growth site. We shall examine these aspects of Eq. (6.23) in the next section. We conclude this section with a numerical example which concerns the stationary-state radical concentration for a typical system. [Pg.363]

The reverberation time in a room is direcdy proportional to the volume and inversely proportional to the amount of sound absorption in the room. For most practical purposes the reverberation time is determined by the Sabine equation ... [Pg.312]

N. A. Tananaev, simultaneously with F. Feigl, developed the spot analysis. Known Tserevitinov method for determining labile hydrogen atoms in organic compounds (1902-1907 should be noted (the method was later improved by A.P Terent ev). In the USSR, there were powerful schools in liquid-liquid extraction and inverse voltammetry. [Pg.20]

As a result a new approaehes in DCP-ai e atomie-emission speetrometry were applied for Ca, Mg, Cu, Zn, Fe and P determination in blood semm and Ca, Mg, Cu, Zn, Fe, P, Mn, Pb, Cd, Sn, Sr et al. - in human and animals hair with relative standai d deviation (RSD) about 10-20 %. The aeeuraey eontrol has been realized by a eomparison of data produeed with the results of independent methods (atomie-absorption speetrometry and inverse voltammetry). [Pg.226]

The SSW form an ideal expansion set as their shape is determined by the crystal structure. Hence only a few are required. This expansion can be formulated in both real and reciprocal space, which should make the method applicable to non periodic systems. When formulated in real space all the matrix multiplications and inversions become 0(N). This makes the method comparably fast for cells large than the localisation length of the SSW. In addition once the expansion is made, Poisson s equation can be solved exactly, and the integrals over the intersitital region can be calculated exactly. [Pg.234]

Just as there is only one direct transform F(s) for any f(t), there is only one inverse transform f(t) for any F(s) and inverse transforms are generally determined through use of tables. [Pg.50]

The rate of the reaction in various buffer solutions, covering the pH range 4-8, was determined, and in hydrogen phosphate-dihydrogen phosphate buffers the rate at constant pH decreased as the concentration of dihydrogen phosphate increased. Similarly, with acetic acid-acetate and phosphoric acid-dihydrogen phosphate buffers the rate was inversely dependent upon the concentration of the molecular acid in addition, with the latter buffer, the kinetic plots showed an unexplained departure from linearity after 50 % reaction. [Pg.363]

Depth of EB penetration The depth of penetration of energetic electrons into a material at normal angle of incidence is directly proportional to the energy of the electrons and inversely proportional to the density of the material [49,50]. The depth is expressed as a product of penetration distance and the density of the material (i.e., 1 g/cm = 1 cm X 1 g/cm ). The radiation energy and thus the type of electron accelerator to be used are dependent on the required penetration depth, the density of the irradiated material, and the chosen irradiation system. If one measures the density (d) in gram per cubic centimeter (g/cm ) and the layer thickness (T) in millimeter (mm), one can determine the radiation energy ( ) necessary for optimal homogeneity from [40] ... [Pg.858]

The pulse duration controls the extent to which the magnetization vectors are bent. A misalignment of the pulse would lead to various artifact signals. Including 180° spin-echo pulses can, to some extent, compensate for setting pulses incorrectly. But in certain experiments (e.g., inverse NMR experiments), it is extremely important for the success of the experiment that the proper pulse angles be determined and employed. [Pg.86]

Electrochemical impedance spectroscopy techniques record impedance data as a function of the frequency of an applied signal at a fixed potential. A large frequency range (65 kHz-1 mHz) must be investigated to obtain a complete impedance spectrum. Dowling et al. and Franklin et al. demonstrated that the small signals required for EIS do not adversely affect the numbers, viability, and activity of microorganisms within a biofilm. EIS data may be used to determine the inverse of the corrosion... [Pg.233]

The order of the mobilities of alachlor, butylate, and metolachlor in columns of various soils was metolachlor > alachlor > butylate. This correlates directly with the water solubilities and inversely to the adsorption coefficients and octanol/water partition coefficients of these compounds. Diffusion of these compounds in soil thin-layers was as follows butylate > alachlor > metolachlor, which correlates directly with the vapor pressures of these compounds. Significant soil properties affecting diffusion appeared to be bulk density and temperature. Soil moisture is also probably important, but its effect on the diffusion of these compounds was not determined. [Pg.231]

The vibrational assignments and force constants have been determined from the IR and Raman spectra of S7NH, S415N4H4 and S415N4D4. The 1H and 15N NMR chemical shifts of all the cyclic sulfur imides have been determined by inverse detection methods.202... [Pg.253]

Negrel Ph, Allegre CJ, Dupre B, Lewin E (1993) Erosion sources determined by inversion of major and trace element ratios and strontium isotopic ratios in river water the Congo Basin case. Earth Planet Sci Lett 120 59-76... [Pg.118]

The group of all real orthogonal matrices of order 3 and determinant +1 will be denoted by 0(3). Such matrices correspond to pure rotation or proper rotation of the coordinate system. An orthogonal matrix with determinant —1 corresponds to the product of pure rotation and inversion. Such transformations are called improper rotations. The matrix corresponding to inversion is the negative of the unit matrix... [Pg.90]

The nonvanishing components of the tensors y a >--eem and ya >-mee can be determined by applying the symmetry elements of the medium to the respective tensors. However, in order to do so, one must take into account that there is a fundamental difference between the electric field vector and the magnetic field vector. The first is a polar vector whereas the latter is an axial vector. A polar vector transforms as the position vector for all spatial transformations. On the other hand, an axial vector transforms as the position vector for rotations, but transforms opposite to the position vector for reflections and inversions.9 Hence, electric quantities and magnetic quantities transform similarly under rotations, but differently under reflections and inversions. As a consequence, the nonvanishing tensor components of x(2),eem and can be different... [Pg.530]

First of all, quantum calculations allow one to predict basicity scales in agreement with experiment provided that the calculations are performed on the preferred conformation of the isolated molecule. If this is not done, a given term within a consistent series may jump from one rank to another as a function of the conformation used for the calculations. The determinant role of preferred conformation on any property (barrier to internal rotation and inversion, dipole moment, first adiabatic ionization potential, acidity and basicity in the gas phase, energy of complexation to BF3, etc.) was clearly demonstrated. We further show the importance of the role of preferred conformation in explaining some of the anomalies in Drago s systematics. [Pg.18]

Allegre, C. J., Hart, S. R. Minster, J.-F. (1983). Chemical structure and evolution of the mantle and the continents determined by inversion of Nd and Sr isotopic data, I. Theoretical models. Earth Planet. Sci. Letters, 66, 177-90. [Pg.526]


See other pages where Determinant and inverse is mentioned: [Pg.61]    [Pg.515]    [Pg.56]    [Pg.142]    [Pg.19]    [Pg.61]    [Pg.515]    [Pg.56]    [Pg.142]    [Pg.19]    [Pg.235]    [Pg.64]    [Pg.237]    [Pg.113]    [Pg.27]    [Pg.207]    [Pg.143]    [Pg.185]    [Pg.186]    [Pg.585]    [Pg.607]    [Pg.227]    [Pg.407]    [Pg.516]    [Pg.242]    [Pg.311]    [Pg.386]    [Pg.553]    [Pg.237]    [Pg.309]    [Pg.62]    [Pg.608]    [Pg.43]   
See also in sourсe #XX -- [ Pg.19 ]




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