Autocatalytic Reaction - Phase Transitions

Phase Transitions

The initial amounts of reactants determine the distance from chemical equilibrium of the system. The greater the initial concentrations the further the system is from equilibrium. As the initial concentration increases, an abrupt change in order occurs. This abrupt change is known as phase transition. At the phase transition, fluctuations in macroscopic quantities, such as chemical concentrations, increase as the system oscillates between the more ordered state (lower entropy, such as ice water) and the more disordered state (higher entropy, such as liquid water). Also, at the phase transition, macroscopic equations, such as the rate equations, fail. Rate equations can be derived from microscopic considerations. The derivations typically rely on a mean field theory approximation to microscopic dynamical equations. Mean field theory breaks down in the presence of large fluctuations (see Mean field theory article for a discussion). Therefore, since large fluctuations occur in the neighborhood of a phase transition, macroscopic equations, such as rate equations, fail. As the initial concentration increases further, the system settles into an ordered state in which fluctuations are again small. (see Prigogine reference)

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