The perturbative phase

For a mathematical treatment of synchronization we recall that the phase of an oscillator is neutrally stable and can be adjusted by a small action, whereas the amplitude is stable. This property allows a description of the effect of small forcing/coupling within the framework of the phase approximation. Considering the simplest case of a limit cycle oscillator, driven by a periodic force with frequency u> and amplitude e, we can write the equation for the perturbed phase dynamics in the form... 

In case of cluster fragmentation models color-singlet clusters of partons form after the perturbative phase of jet development and then decay into the observed hadrons. The clusters originate from gluon splitting in quark pairs and subsequent recombination with neighboring quarks and antiquarks. Afterward, the clusters are assumed to decay isotropically in their rest frame into pairs of hadrons, where the branching ratios are determined by the density of states. 

Because the perturbation is Hamiltonian, the 3D level energy surfaces are preserved. In the 4D normally hyperbolic invariant manifold of the unperturbed space, the locally stable and unstable manifolds and the flow describe the geometric structure of the perturbed phase space given by the perturbed normally hyperbolic locally invariant manifold, the locally stable and unstable manifolds, and the persistence of the 2D nonresonant invariant tori T-,(Pi,P2)-... 

Perturbation or relaxation techniques are applied to chemical reaction systems with a well-defined equilibrium. An instantaneous change of one or several state fiinctions causes the system to relax into its new equilibrium [29]. In gas-phase kmetics, the perturbations typically exploit the temperature (r-jump) and pressure (P-jump) dependence of chemical equilibria [6]. The relaxation kinetics are monitored by spectroscopic methods. 

As discussed in detail in [10], equivalent results are not obtained with these three unitary transformations. A principal difference between the U, V, and B results is the phase of the wave function after being h ansported around a closed loop C, centered on the z axis parallel to but not in the (x, y) plane. The pertm bative wave functions obtained from U(9, <])) or B(0, <()) are, as seen from Eq. (26a) or (26c), single-valued when transported around C that is ( 3 )(r Ro) 3< (r R )) = 1, where Ro = Rn denote the beginning and end of this loop. This is a necessary condition for Berry s geometric phase theorem [22] to hold. On the other hand, the perturbative wave functions obtained from V(0, <])) in Eq. (26b) are not single valued when transported around C. 

Bash, P.A., Field, M.J.,Karplus, M. Free energy perturbation method for chemical reactions in the condensed phase A dynamical approach baaed on a combined quantum and molecular dynamics potential. J. Am. Chem. Soc. 109 (1987) 8092-8094. 

It is often the case that the solvent acts as a bulk medium, which affects the solute mainly by its dielectric properties. Therefore, as in the case of electrostatic shielding presented above, explicitly defined solvent molecules do not have to be present. In fact, the bulk can be considered as perturbing the molecule in the gas phase , leading to so-called continuum solvent models [14, 15]. To represent the electrostatic contribution to the free energy of solvation, the generalized Bom (GB) method is widely used. Wilhin the GB equation, AG equals the difference between and the vacuum Coulomb energy (Eq. (38)) ... 

A second method is to use a perturbation theory expansion. This is formulated as a sum-over-states algorithm (SOS). This can be done for correlated wave functions and has only a modest CPU time requirement. The random-phase approximation is a time-dependent extension of this method. 

RPA, and CPHF. Time-dependent Hartree-Fock (TDFIF) is the Flartree-Fock approximation for the time-dependent Schrodinger equation. CPFIF stands for coupled perturbed Flartree-Fock. The random-phase approximation (RPA) is also an equivalent formulation. There have also been time-dependent MCSCF formulations using the time-dependent gauge invariant approach (TDGI) that is equivalent to multiconfiguration RPA. All of the time-dependent methods go to the static calculation results in the v = 0 limit. 

AH distortions of the nematic phase may be decomposed into three basic curvatures of the director, as depicted in Figure 6. Liquid crystals are unusual fluids in that such elastic curvatures may be sustained. Molecules of a tme Hquid would immediately reorient to flow out of an imposed mechanical shear. The force constants characterizing these distortions are very weak, making the material exceedingly sensitive and easy to perturb. 

Natural linewidths are broadened by several mechanisms. Those effective in the gas phase include collisional and Doppler broadening. Collisional broadening results when an optically active system experiences perturbations by other species. Collisions effectively reduce the natural lifetime, so the broadening depends on a characteristic impact time, that is typically 1 ps at atmospheric pressure ... 

The fugacity coefficient of thesolid solute dissolved in the fluid phase (0 ) has been obtained using cubic equations of state (52) and statistical mechanical perturbation theory (53). The enhancement factor, E, shown as the quantity ia brackets ia equation 2, is defined as the real solubiUty divided by the solubihty ia an ideal gas. The solubiUty ia an ideal gas is simply the vapor pressure of the sohd over the pressure. Enhancement factors of 10 are common for supercritical systems. Notable exceptions such as the squalane—carbon dioxide system may have enhancement factors greater than 10. Solubihty data can be reduced to a simple form by plotting the logarithm of the enhancement factor vs density, resulting ia a fairly linear relationship (52). 

Flow markers are often chosen to be chemically pure small molecules that can fully permeate the GPC packing and elute as a sharp peak at the total permeation volume (Vp) of the column. Examples of a few common flow markers reported in the literature for nonaqueous GPC include xylene, dioctyl phthalate, ethylbenzene, and sulfur. The flow marker must in no way perturb the chromatography of the analyte, either by coeluting with the analyte peak of interest or by influencing the retention of the analyte. In all cases it is essential that the flow marker experience no adsorption on the stationary phase of the column. The variability that occurs in a flow marker when it experiences differences in how it adsorbs to a column is more than sufficient to obscure the flow rate deviations that one is trying to monitor and correct for. 

The operation involved in the definition of the EPI is an exchange of atoms on sites i and j and it is a kind of localized perturbation. So the orbital peeling method provides an efficient means for obtaining the generalized phase shifts. 

Infinite Systems The ultimate fate of infinite systems, in the infinite time limit, is quite different from their finite cousins. In particular, the fate of infinite systems does not depend on the initial density of cr = 1 sites. In the thermodynamic limit, there will always exist, with probability one, some convex cluster large enough to grow without limit. As f -4 oo, the system thus tends to p —r 1 for all nonzero initial densities. What was the critical density for finite systems, pc, now becomes a spinodal point separating an unstable phase for cr = 0 sites for p > pc from a metastable phase in which cr = 0 and cr = 1 sites coexist. For systems in the metastable phase, even the smallest perturbation can induce a cluster that will grow forever. 

According to Fig. 2, as M comes in contact with S,3 4 the electron distribution at the metal surface (giving the surface potential XM) will be perturbed X ) The same is the case for the surface orientation of solvent molecules (Xs + SXS). In addition, a potential drop has to be taken into account at the free surface of the liquid layer toward the air (xs). On the whole, the variation of the electron work function (if no charge separation takes place as assumed at the pzc of a polarizable electrode) will measure the extent of perturbation at the surfaces of the two phases, i.e.,... 

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