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Flux-side correlation function

However, further analysis of the linear regression expression in A3.8.1 is required to achieve a useful expression for the rate constant both from a computational and a conceptual points of view. Such an expression was first provided by Yamamoto [6], but others have extended, validated, and expounded upon his analysis in considerable detail [7, 8]. The work of Chandler [7] in this regard is followed most closely here in order to demonstrate the places in which condensed phase effects can appear in the theory, and hence in the value of the thermal rate constant. The key mathematical step is to differentiate both sides of the linear regression formula in (A3.8.1) and then carefully analyse its expected behaviour for systems having a barrier height of at least several times k-Q T. The resulting expression for the classical forward rate constant in terms of the so-called reactive flux time correlation function is given by [6, 7 and 8]... [Pg.885]

The shell side heat transfer coefficient (ho) is calculated as the sum of the convective and nucleate boiling heat transfer coefficients he and hn respectively). Both hi (the inside tube coefficient) and he are given in terms of tube diameters, thermal conductivities, vapour and liquid densities and Reynolds and Prandtl numbers in the appropriate streams by standard correlations [25]. hn is given as a function of heat flux, pressure and solvent critical pressure by the Mostinski equation [26]. [Pg.317]

Example 3.4.3 Schaetzel et al. (2004) have studied the per-vaporation of a water-ethanol mixture through a polyvinylalcohol based membrane as a function of feed water concentration at 60 °C. They have also measured the equilibrium volume fraction of water and ethanol in the membrane for such feed mixtures. When there is very high vacuum in the permeate side, it is possible to correlate the water flux (mol/m -s) with the feed side water and ethanol volume fractions CaHjOH.mlo- respectively,... [Pg.177]

When evaporation is present, two-phase heat transfer should be taken into consideration. A number of correlations have been derived to predict the critical heat flux condition as a function of temperature difference between the fluid and the heated surface. A comparison between the predicted and experimental heat flux values is shown in Figs. 5.6-5.8 for hydrogen, nitrogen, and oxygen, respectively. The evaporation usually occurs on the shell side. [Pg.199]


See other pages where Flux-side correlation function is mentioned: [Pg.308]    [Pg.179]    [Pg.308]    [Pg.179]    [Pg.67]    [Pg.204]   
See also in sourсe #XX -- [ Pg.288 ]




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