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Phase frozen

Me3SnCl (33) 119Sn Mossbauer. The frozen solid compound is polymeric, while die compound isolated in a low-temperature argon matrix is monomeric as in die gas phase. Frozen solutions in polar solvents show significant solvent solute interactions. Compare to behaviour of compound 79 in Table 8. 154... [Pg.385]

Warm water evaporates, but so does cool water. The only difference is that cool water evaporates at a slower rate. Even frozen water evaporates. This form of evaporation, in which molecules jump directly from the solid phase to the gaseous phase, is called sublimation. Because water molecules are so firmly held in the solid phase, frozen water does not release molecules into the gaseous phase as readily as liquid water does. Sublimation, however, does account for the loss of significant portions of snow and ice, especially on sunny, dry mountain tops. It s also why ice cubes left in the freezer for a long time tend to get smaller. [Pg.269]

Darby, R. On two-phase frozen and flashing flows in safety relief valves. J. Loss Prev. Process Ind. 2004, 17 (4), 255-259. [Pg.2437]

Figure 1. Cross section through a number of lipid-water phases. Frozen (gel) chain phases (b, c), lamellar phases (a, b, c), and hexagonal phases (d, e) are shown. Figure 1. Cross section through a number of lipid-water phases. Frozen (gel) chain phases (b, c), lamellar phases (a, b, c), and hexagonal phases (d, e) are shown.
Consider how the change of a system from a thennodynamic state a to a thennodynamic state (3 could decrease the temperature. (The change in state a —> f3 could be a chemical reaction, a phase transition, or just a change of volume, pressure, magnetic field, etc). Initially assume that a and (3 are always in complete internal equilibrium, i.e. neither has been cooled so rapidly that any disorder is frozen in. Then the Nemst heat... [Pg.371]

The molecular constants that describe the stnicture of a molecule can be measured using many optical teclmiques described in section A3.5.1 as long as the resolution is sufficient to separate the rovibrational states [110. 111 and 112]. Absorption spectroscopy is difficult with ions in the gas phase, hence many ion species have been first studied by matrix isolation methods [113], in which the IR spectrum is observed for ions trapped witliin a frozen noble gas on a liquid-helium cooled surface. The measured frequencies may be shifted as much as 1 % from gas phase values because of the weak interaction witli the matrix. [Pg.813]

To deal with the problem of using a superposition of functions, Heller also tried using Gaussian wave packets with a fixed width as a time-dependent basis set for the representation of the evolving nuclear wave function [23]. Each frozen Gaussian function evolves under classical equations of motion, and the phase is provided by the classical action along the path... [Pg.275]

The Hemian-Kluk method has been developed further [153-155], and used in a number of applications [156-159]. Despite the formal accuracy of the approach, it has difficulties, especially if chaotic regions of phase space are present. It also needs many trajectories to converge, and the initial integration is time consuming for large systems. Despite these problems, the frozen Gaussian approximation is the basis of the spawning method that has been applied to... [Pg.275]

While it is not essential to the method, frozen Gaussians have been used in all applications to date, that is, the width is kept fixed in the equation for the phase evolution. The widths of the Gaussian functions are then a further parameter to be chosen, although it appears that the method is relatively insensitive to the choice. One possibility is to use the width taken from the harmonic approximation to the ground-state potential surface [221]. [Pg.297]

As usual there is the question of the initial conditions. In general, more than one frozen Gaussian function will be required in the initial set. In keeping with the frozen Gaussian approximation, these basis functions can be chosen by selecting the Gaussian momenta and positions from a Wigner, or other appropriate phase space, distribution. The initial expansion coefficients are then defined by the equation... [Pg.297]

The product must be formulated and frozen in a manner which ensures that there is no fluid phase remaining. To achieve this, it is necessary to cool the product to a temperature below which no significant Hquid—soHd phase transitions exist. This temperature can be deterrnined by differential scanning calorimetry or by measuring changes in resistivity (94,95). [Pg.530]

Component Separation by Progressive Freezing When the distribution coefficient is less than I, the first solid which ciystaUizes contains less solute than the liquid from which it was formed. As the frac tion which is frozen increases, the concentration of the impurity in the remaining liquid is increased and hence the concentration of impurity in the sohd phase increases (for k < 1). The concentration gradient is reversed for k > 1. Consequently, in the absence of diffusion in the solid phase a concentration gradient is estabhshed in the frozen ingot. [Pg.1990]

If the bulk-liquid phase is well mixed and no diffusion occurs in the solid phase, a simple expression relating the solid-phase composition to the frac tion frozen can be obtained for the case in which the distribution coefficient is independent of composition and fraction frozen... [Pg.1990]

Low temperatures can cause a phase separation in stabilized solutions in which case one phase can become deficient in stabilizer and subject to runaway reactions. Acrylic acid can crystallize out of stabilized solution, and subsequent thawing of these essentially pure acrylic acid crystals can initiate runaway reactions, often with severe consequences. Thawing of crystallized (frozen) materials needs to be accomplished using established procedures in thaw boxes or similar devices. If established procedures are not available, a safety review needs to be conducted and a procedure developed prior to thawing the material. [Pg.107]

At room temperature, diffusion is so slow that the alloy just stays like this, frozen as a single phase. But if you heat it up just a little - to 160°C, for example - and hold it there ("ageing"), the copper starts to diffuse together to form an enormous number of very tiny (nm) plate-like particles, of composition roughly CuAlj. On recooling to room temperature, this new structure is again frozen in. [Pg.324]


See other pages where Phase frozen is mentioned: [Pg.12]    [Pg.12]    [Pg.517]    [Pg.1098]    [Pg.2292]    [Pg.275]    [Pg.380]    [Pg.439]    [Pg.43]    [Pg.157]    [Pg.120]    [Pg.454]    [Pg.335]    [Pg.339]    [Pg.255]    [Pg.430]    [Pg.496]    [Pg.306]    [Pg.433]    [Pg.152]    [Pg.1990]    [Pg.55]    [Pg.223]    [Pg.42]    [Pg.85]    [Pg.10]    [Pg.43]    [Pg.311]    [Pg.82]    [Pg.84]    [Pg.380]    [Pg.144]    [Pg.971]    [Pg.159]    [Pg.472]   
See also in sourсe #XX -- [ Pg.522 , Pg.525 , Pg.555 , Pg.560 ]




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