ABSTRACT
Precipitation patterns emerging in a two-dimensional moving front are investigated on the example of NaOH diffusing into a gel containing AlCl3 . The time evolution of the precipitate Al(OH)_{3} can be observed since the precipitate redissolves in the excess outer electrolyte NaOH and thus it exists only in a narrow optically accessible region of the reaction front. The patterns display self-similar coarsening with a characteristic length xi increasing with time as xi(t) approximately sqrt[t] . A theory based on the Cahn-Hilliard phase-separation dynamics, including redissolution, is shown to yield agreement with the experiments.
ABSTRACT
Understanding and controlling precipitation patterns formed in reaction-diffusion processes is of fundamental importance with high potential for technical applications. Here we present a theory showing that precipitation resulting from reactions among charged agents can be controlled by an appropriately designed, time-dependent electric current. Examples of current dynamics yielding periodic bands of prescribed wavelength, as well as more complicated structures are given. The pattern control is demonstrated experimentally using the reaction-diffusion process 2AgNO3 + K2Cr2O7-->under Ag2Cr2O7 + 2KNO3.
