Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Diffusion displacements

The plasma potential is the maximum value with which ions can be accelerated from the edge of the sheath towards the substrate, located at the grounded electrode. This may cause ion bombardment, which may induce ion-surface interactions such as enhancement of adatom diffusion, displacement of surface atoms, trapping or sticking of incident ions, sputtering, and implantation see Section 1.6.2.1. [Pg.29]

Another type of flow artifact is due to voxel inflow and outflow problems large velocities make a spin leave its designated voxel in the time between signal encoding and signal readout. As the traveled distance d and the velocity v are related by the expression d = vt, it is obvious that the effect is more severe, the smaller the voxel size is. Slow velocities, on the other hand, may be masked by diffusive displacements. [Pg.214]

Self-diffusion in simple monatomic liquids at temperatures well above their glass-transition temperatures may be interpreted in a simple manner.1 Within such liquids, regions with free volume appear due to displacement fluctuations. Occasionally, the fluctuations are large enough to permit diffusive displacements. [Pg.229]

CTTS transitions, in which the oriented solvent participates are absent in the spectrum of the aromatic solutes but the lifetime of the excited state, as shown by the existence of fluorescence is longer, probably 10 9 sec. During this extended lifetime, sufficient reorganization of the solvent may occur to enable the excited electron to be trapped, and to allow for the first relative diffusive displacement of the gemini, which is necessary for the observed kinetics to develop. The temperature ef-... [Pg.243]

Theoretical arguments are twofold. On one hand, one may expect that e+ also gets solvated over a time comparable with r . Mobility of solvated particles drastically drops and they simply do not have enough time to meet each other during the free-positron lifetime ( 0.5 ns). Really, corresponding diffusion displacement of e+ is smaller than e+ thermalization... [Pg.133]

Fig. 5.35. Schematic diagrams to indicate how diffusive displacement can occur through a coordinated movement of a pair of ions into a paired... Fig. 5.35. Schematic diagrams to indicate how diffusive displacement can occur through a coordinated movement of a pair of ions into a paired...
Now, we have to identify V2 and Vu. To do so, we consider the case of two connected stochastic processes where each process is a diffusion type with two states. The example concerns one marked particle that is subjected to a two-state diffusion displacement. The particle can be considered as a molecular species (so the particle movement describes a mass transport process) and we can also take into account the total enthalpy of the process (heat transport process). This particular case of stochastic model, can be described with the assembly of relations (4.79). In the model, the mean probability of the existence of local species (e nj) and the mean probability of the existence of local enthalpy (ej 2) given by the assembly... [Pg.240]

In Eqs. (4.153) and (4.154), we recognize the general case of an unsteady state diffusion displacement in a solid body. [Pg.248]

Several different processes lead to the band-spreading phenomena in the column which include multipath effect molecular diffusion displacement in the porous beds secondary equilibria and others. Each of these processes introduces its own degree of variance toward the overall band-spreading process. Usually these processes are assumed to be independent and based on the fundamental statistical law, overall band-spreading (variance) is equal to the sum of the variances for each independent process ... [Pg.28]

Both p and m can be expressed in terms of the basic quantities p (the encounter diameter), o (the root mean square displacement for relative diffusion motion), and v (the frequency of relative diffusion displacements) as [3]... [Pg.27]

The lifetime of encounter complexes between neutral reactants is on the order of 0.1 ns in solvents of low viscosity, that is, k d kd m. Random diffusive displacements of the order of a molecular diameter occur with a frequency of about 1011 s Subsequently, the fragments from a specific dissociation may re-encounter each other and undergo secondary recombination .59 If secondary recombination does not take place within about 1 ns, the fragments will almost certainly have diffused so far apart that the chance of a reencounter becomes negligible. The initial overall electronic multiplicity 2S + 1 of encounter complexes is thus important in determining the fate of the reactants, because their lifetime is usually insufficient to allow for intersystem crossing during an encounter. [Pg.46]

Tsige and Taylor s work on syndiotactic poly(methyl methacrylate) (68) indicated that atomistic molecular dynamic simulations can provide useful information about the nature of the glass transition in polymers via computational runs of modest size, especially if an uncomplicated force field is used in order to help reach the difiiisive regime with modest computational resources. It was also found that the subtraction of the oscillatory contribution to the motion is a useful tool for revealing the time variation of diffusive displacements. [Pg.553]

A schematic representation of the situation one is dealing with in this context is shown in Fig. 37. We consider the representative segments kon chain a and I on chain p. The internuclear vector, 7ki t), fluctuates because of self-diffusive displacements Rrei t) of segment I relative to segment k. That is, the origin of the reference frame is considered to be fixed at segment k. [Pg.87]


See other pages where Diffusion displacements is mentioned: [Pg.70]    [Pg.250]    [Pg.101]    [Pg.61]    [Pg.292]    [Pg.9]    [Pg.12]    [Pg.182]    [Pg.662]    [Pg.88]    [Pg.173]    [Pg.417]    [Pg.474]    [Pg.499]    [Pg.70]    [Pg.733]    [Pg.11]    [Pg.12]    [Pg.12]    [Pg.135]    [Pg.38]    [Pg.38]    [Pg.98]    [Pg.331]    [Pg.140]    [Pg.12]    [Pg.47]   
See also in sourсe #XX -- [ Pg.229 ]

See also in sourсe #XX -- [ Pg.81 ]




SEARCH



Anomalous diffusion mean-square displacement

Diffusion and Root-Mean-Square Displacement

Diffusion molecular displacements larger than

Diffusivity mean square displacement

Displacement response time-dependent diffusion coefficient

Mean square displacement diffusion

Self-diffusion mean-square displacement

© 2024 chempedia.info