On the kinetics of consecutive, bimolecular reactions

Modeling the kinetics of bimolecular reactions.

ion reaction, after the ZPE contributions are included there is no barrier in the effective potential along the reaction coordinate, so important variational effects are expected. Both VMEP and the vibrationally adiabatic potential are plotted along the path in Figure 1. At room temperature the maximum of the free energy (see eq 2.4.36) is located at s* CVT ) -0.364 a0, whereas s* μVT is energy...

The effect of initial spatial correlations on late time kinetics of bimolecular irreversible reactions

We study anomalous kinetics associated with incomplete mixing for a bimolecular irreversible kinetic reaction where the underlying transport of reactants is governed by a fractional dispersion equation. As has been previously shown, we demonstrate that at late times incomplete mixing effects dominate and the decay of reactants follows a fundamentally different scaling comparing to the idealized...

Kinetics of consecutive reactions in the solid state:

The thermal and kinetic aspects of solid state decomposition reactions can be complex and posses a large number of parameters to investigate. The determination of the activation energies for the several intermediates in the thermal decomposition is particularly sensitive to the overlap in thermal decomposition traces. To overcome this problem we have undertaken the detailed kinetic analysis of ...

Interpretation of the kinetics of consecutive enzyme-catalyzed reactions. Studies on the arginase-urease system.

Physiocochemical properties of beef liver arginase are reported, particular attention being given to its state of aggregation in the concentration range encountered in enzymic assays. It is shown that a species of molecular weight 114,000 is the operational kinetic unit. Evidence is also provided that arginase does not associate heterogeneously with urease, and therefore, in the absence of macr...

Note on the Simple Collision Theory of Bimolecular Reactions.