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INDEX relaxation

For sufficiently long times (index n ), the exponential can be neglected, leaving an oscillation of the turnover variable phase shifted with respect to the sound wave and with its amplitude reduced by the finite relaxation... [Pg.2122]

Suppose we divide the flow segments into classes according to relaxation times and index the various states by the subscript i. Thus the relaxation time and the component of shear stress borne by the segments in class i are and Fj, respectively. The applied shear force is related to the Fj s through... [Pg.101]

We have also deduced from our simulations the relaxed positions of Au adatom in the perpendicular to the surface direction. In Figure 5 we give the percentage relaxation of Au on the low-index faces of Cu, with respect to the bulk interlayer spacing of the latter, as a function of temperature. We observe at room temperature, an important contraction of the relaxed position of Au adatom (= 16%), which is more pronounced than in the case of Cu adatom (= 11%). As the temperature increases, the adatom presents stronger contractions on Cu(l 10) than on the other faces, in agreement with the MSD results, attaining at 1000"K a value of -60%. [Pg.155]

Figure 5. Temperature dependence of percentage relaxation of Au adatom on the low-index faces of Cu with respect to the bulk interlayer spacing. Figure 5. Temperature dependence of percentage relaxation of Au adatom on the low-index faces of Cu with respect to the bulk interlayer spacing.
We have studied the vibrational properties of Au adatoms on the low-index faces of copper. From the position of new phonon modes, which are due to the presence of the adatom, it comes out that the gold adatom is weakly coupled with the atoms of Cu(l 11) for the directions parallel to the surface and tightly bound with those of Cu(lOO). These modes are found in lower frequencies than those of the Cu adatom. The temperature dependence of MSD s and relaxed positions of the Au adatom along the normal to the surface direction, reveal that this atom is more tightly bound with the (111) face and less with the (110) face. [Pg.155]

Being applied for the relaxation of populations (k = 0), this equality expresses the demands of the detailed balance principle. This is simply a generalization of Eq. (4.25), which establishes the well-known relation between rates of excitation and deactivation for the rotational spectrum. It is much more important that equality (5.21) holds not only for k = 0 but also for k = 1 when it deals with relaxation of angular momentum J and the elements should not be attributed any obvious physical sense. The non-triviality of this generalization is emphasized by the fact that it is impossible to extend it to the elements of the four-index... [Pg.161]

Generally speaking, neither dynamical, nor relaxation parts of (A7.20) are diagonal over index q. It is simpler to diagonalize the dynamical term, proceeding to the GF, where scalar product (j L) = (JzLq) =... [Pg.271]

In the MF equation (A7.20) can be simplified essentially only in the particular case of non-adiabatic collisions, which do not change the molecular orientation y(g) = <5(g). In this case operator T = /, and the relaxation part of (A7.20) can be diagonalized over index q ... [Pg.271]

Accurate interpretation of the formation properties (porosity, permeability and irreducible water saturation) requires reliable estimates of NMR fluid properties or the relationship between diffusivity and relaxation time. Estimation of oil viscosity and solution-gas content require their correlation with NMR measurable fluid properties. These include the hydrogen index, bulk fluid relaxation time and bulk fluid diffusivity [8]. [Pg.324]

Porosity (ej>) determination with NMR is a direct measurement as the response is from the fluid(s) in the pore space of the rock. The initial amplitude (before relaxation) of the NMR response of the fluid(s) saturated rock (corrected for hydrogen index) is compared with the amplitude of the response of bulk water having the same volume as the bulk volume of the rock sample. The 2 MHz NMR... [Pg.326]

Interpretation of NMR well logs is usually made with the assumption that the formation is water-wet such that water occupies the smaller pores and oil relaxes as the bulk fluid. Examination of crude oil, brine, rock systems show that a mixed-wet condition is more common than a water-wet condition, but the NMR interpretation may not be adversely affected [47]. Surfactants used in oil-based drilling fluids have a significant effect on wettability and the NMR response can be correlated with the Amott-Harvey wettability index [46]. These surfactants can have an effect on the estimation of the irreducible water saturation unless compensated by adjusting the T2 cut-off [48]. [Pg.336]

In order to be able to evaluate data with a reasonable number of parameters, the mode analysis assumes, as a first approximation, that the exponential correlation of the correlations [Eq. (18)] is maintained, and only the relaxation rates 1/tp are allowed to depend on a general form on the mode index... [Pg.26]

Figure 14 shows the results for Wp, the mode-dependent relaxation rate, for the different molecular masses as a function of the mode index p. For the smallest molecular mass Mw = 2000 g/mol relaxation rates Wp are obtained which are independent of p. This chain obviously follows the Rouse law. The modes relax at a rate proportional to p2 [Eq. (17)]. If the molecular weight is increased, the relaxation rates are successively reduced for the low-index modes in comparison to the Rouse relaxation, whereas the higher modes remain uninfluenced within experimental error. [Pg.30]

Fig. 2. Relaxation modulus G(t) of a set of polydimethylsiloxane samples with increasing extent of crosslinking plotted against time of crosslinking. The linear PDMS chains (Mn 10 000, polydis-persity index 2) were endlinked with a four-functional silane crosslinker catalyzed by a platinum compound. Samples with different extent of reaction were prepared by poisoning the reaction at different times. The actual extent of reaction was not determined. Two of the samples are clearly before the gel point (LST) and two beyond. The third sample is very close to the gel point. Data of Chambon and Winter [5] evaluated by Baumgartel and Winter [8]... Fig. 2. Relaxation modulus G(t) of a set of polydimethylsiloxane samples with increasing extent of crosslinking plotted against time of crosslinking. The linear PDMS chains (Mn 10 000, polydis-persity index 2) were endlinked with a four-functional silane crosslinker catalyzed by a platinum compound. Samples with different extent of reaction were prepared by poisoning the reaction at different times. The actual extent of reaction was not determined. Two of the samples are clearly before the gel point (LST) and two beyond. The third sample is very close to the gel point. Data of Chambon and Winter [5] evaluated by Baumgartel and Winter [8]...

See other pages where INDEX relaxation is mentioned: [Pg.185]    [Pg.187]    [Pg.577]    [Pg.185]    [Pg.187]    [Pg.577]    [Pg.541]    [Pg.1079]    [Pg.2222]    [Pg.2672]    [Pg.97]    [Pg.163]    [Pg.134]    [Pg.204]    [Pg.259]    [Pg.248]    [Pg.20]    [Pg.274]    [Pg.612]    [Pg.408]    [Pg.275]    [Pg.494]    [Pg.114]    [Pg.282]    [Pg.324]    [Pg.418]    [Pg.199]    [Pg.30]    [Pg.35]    [Pg.249]    [Pg.9]    [Pg.10]   
See also in sourсe #XX -- [ Pg.58 ]




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