Crystal Growth from Aqueous Solution in the Presence of Structured Impurities

Abstract

A kinetic model describing crystal growth from aqueous solution in the presence of structured impurities is developed on a generalization in the spirit of the Davey and Mullin model. The proposed theoretical framework combines (i) an analytical expression for the step velocity, where this quantity decreases linearly with increasing surface coverage (θeq) by impurities adsorbed on the growing crystal, and (ii) a new adsorption isotherm equation θeq(C I) (C I is the concentration of impurities) in which the adsorbate can occupy more than one adsorption site (structured impurity). The formalism leads to the exact adsorption isotherm of linear rods in one dimension and provides a close approximation for two-dimensional systems accounting for multisite occupancy. Moreover, the model is capable of predicting the effect of size/shape of the impurities from parameters having a precise physical meaning. These parameters can be obtained from thermodynamic experiments and are related directly to the spatial configuration of the impurity molecules in the adsorbed state. The theoretical results are contrasted with Monte Carlo simulations and experimental data of the relative growth rates of the {100} faces of KBr crystals in the presence of impurity molecules (linear aliphatic carboxylic acids) of different sizes. A good agreement between theory, simulations, and experiments is found.

Modulation of the electrostatic potential around α-lactalbumin using oligoelectrolyte chains, pH and salt concentration

“…This finding is consistent with previous theoretical and experimental work corresponding to systems in the presence of multisite-occupancy adsorption (adsorption of objects that occupy more than one site on the substrate). [48][49][50][51] As shown in ref. [48][49][50][51], the adsorbed amount increases with the adsorbate size and binding area (number of binding sites per adsorbate molecule).…”

“…[48][49][50][51] As shown in ref. [48][49][50][51], the adsorbed amount increases with the adsorbate size and binding area (number of binding sites per adsorbate molecule).…”