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The specific rate function k E as an inverse Laplace transform

At infinite pressure, as we argued in Chapter 1, the rate of replenishment of the reactive molecular states is so fast that even allowing for the decay processes, the populations of these states remain at their Boltzmann equilibrium values. Hence, we can write [Pg.34]

1 It is convenient at some point to slide over from the molecular units e, k, as used in equations (3.10H3.13), to the practical units E, R, used by practising kineticists. [Pg.34]

2 For a few molecules which span our general range of interest, e.g. CO2, CHjNC, cyclo-C4H8, C2F6, the densities of (rotation-vibration) states at the thermal thresholds are approximately 10 , 10 , 10 , 10 states per wavenumber respectively. [Pg.34]


The specific rate function k(E) as an inverse Laplace transform... [Pg.34]




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E function

Functional specific

Functional specifications

Inverse Laplace transforms

Inverse function

Inverse transform

Inversion Laplace transforms

Inversion rate

K function

Laplace

Laplace - inverse transform function

Laplace inversion

Laplace transform

Laplace transform function

Laplace transform inversion

Laplace transforms

Rating function

Specific Functionalities

Specific rate

Specific rate function

Specific transformation

Specificity function

The Laplace transform

Transformation function

Transformation inversion

Transformation rate

Transforms Laplace transform

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