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Diffusion-mean termination models

The iGLE also presents a novel approach for studying the reaction dynamics of polymers in which the chemistry is driven by a macroscopic force that is representative of the macroscopic polymerization process itself The model relies on a redefined potential of mean force depending on a coordinate R which corresponds locally to the reaction-path coordinate between an n-mer and an (n -t 1 )-mer for R = nl. The reaction is quenched not by a kinetic termination step, but through an (R(t))-dependent friction kernel which effects a turnover from energy-diffusion-limited to spatial-diffusion-Iimited dynamics. The iGLE model for polymerization has been shown to exhibit the anticipated qualitative dynamical behavior It is an activated process, it is autocatalytic, and it quenches... [Pg.111]

Airways flow has a boundary condition of diffusion only at the terminal level within the alveolar sacs. While air is moved in and out in the upper respiratory system, diffusion is die means by which material is shifted near the lung-blood interfaces. A flow model of the lower respiratory system should be such that air does not physically move in and out of the alveolar sacs. [Pg.226]

Because of the relatively short displacement time or length scales typically probed by NMR diffusometry, it is particularly well suited to detect anomalies in the segment displacement behavior expected on a time scale shorter than the terminal relaxation time, that is for root mean squared displacements shorter than the random-coil dimension. All models discussed above unanimously predict such anomalies (see Tables 1-3). Therefore, considering exponents of anomalous mean squared displacement laws alone does not provide decisive answers. In order to obtain a consistent and objective picture, it is rather crucial to make sure that (i) the absolute values of the mean squared segment displacement or the time-dependent diffusion coefficient are compatible with the theory, (ii) the dependence on other experimental parameters such as the molecular weight are correctly rendered, and (iii) the values of the limiting time constants are not at variance with those derived from other techniques. [Pg.99]


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See also in sourсe #XX -- [ Pg.32 ]




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