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Enthalpy, activation external

Dispersive interaction has a dramatic effect on the molecular layers closest to the surface, and can be explained in terms of the rate theory for viscous flow.f Within the rate theory, a flow event comprises the transition of a flow unit from its normal or quiescent state, through a flow-activated state, to a region of lower free energy in an external stress field. For small molecules, the flow unit is the whole molecule, while for longer chains, the flow unit is a segment of the entire molecule. By analogy with chemical reaction rate theory, there is a flow-activation enthalpy, and entropy, for transition into the flow-activated state. [Pg.3081]

The enthalpy change for reaction is exothermic and varies from 50 to 80 kJ/mol. The activation energy for the forward reaction varies from 25 to 27 kJ/mol. The temperature at the external surface of the pellet is constant at 350 K. The effective thermal conductivity of alumina catalysts is 1.6 x 10 J/cm s K. The chemical reaction is first-order and irreversible and the catalysts exhibit rectangular symmetry. When a(0) 1 in the mass transfer equation, simulations in... [Pg.737]

Stoeckli and Centano (1997) showed that, for carbons of low external surface areas, the ratios between the limiting volumes filled by liquids of variable molecular dimension and the micropore volume accessible to a small molecule (when used as a reference) can be closely estimated from enthalpies of immersion. This approach describes the development of porosity during an activation process and the RSDs of the developed microporosity. As a wetting agent, Stoeckli and Centano (1997) used benzene because of the similarity of molecular size with n-butane which cannot be used as a liquid. The majority of the micropores were <0.8 nm in access dimension. [Pg.179]

Following this equation, the relation between the product nd the microporous surface area will not be always the same, but depends on the average pore width L. Thus, for a highly microporous activated carbon, or any other adsorbent with slit-shaped pores with a low external surface area, the enthalpy of immersion is proportional to the product EqWq but not to the microporous surface area 5. Anyway, Eq can be estimated from Equation (4.15) for a given liquid, this allowing for the calculation of micropore size distributions by using liquids with different molecular sizes, Stoeckli et al. (1990). [Pg.216]

The change in the standard free energy AG of a cell reaction is the driving force which enables a battery to deliver electrical energy to an external circuit. The measurement of the electromotive force, incidentally, also makes available data on changes in free energy, entropies and enthalpies together with activity coefficients, equilibrium constants, and solubility products. [Pg.39]

The heats of formation of chemical elements in standard state are taken as zero. The list of such elements is known, for example, [13] and mainly incorporates elements in solid state. Thus the single-atom gas formation enthalpy in these cases equals the sublimation enthalpy and is determined by physical and chemical criteria of the process. The sublimation comes to diffusion movements of heated particles into the surface layer with further effusion (outflow). The diffusion activation energies in external and internal regions are quite different... [Pg.64]


See other pages where Enthalpy, activation external is mentioned: [Pg.412]    [Pg.65]    [Pg.182]    [Pg.27]    [Pg.271]    [Pg.65]    [Pg.250]    [Pg.50]    [Pg.331]    [Pg.469]    [Pg.106]    [Pg.76]    [Pg.109]    [Pg.144]    [Pg.167]    [Pg.606]    [Pg.120]    [Pg.14]    [Pg.147]    [Pg.254]    [Pg.1145]    [Pg.141]    [Pg.169]    [Pg.28]    [Pg.275]   
See also in sourсe #XX -- [ Pg.462 ]




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