ABSTRACT
The crystal growth of boric acid from an aqueous solution in the absence and presence of sodium and lithium sulfate was studied by real-time monitoring. For this purpose, atomic force microscopy in situ has been used. The results show that the growth mechanism of boric acid from its pure and impure solutions is spiral growth driven by screw dislocation and that the velocity of advancement of steps on the crystal surface, and the relative growth rate (ratio of the growth rate in presence and absence of a salt) is reduced in the presence of salts. The reduction of the relative growth rate could be explained by the inhibition of advancement of steps of the (001) face mainly in the growth direction [100] caused by the adsorption of salts on the actives sites and the inhibition of the formation of sources of steps such as dislocations. The adsorption of the salts on the crystal surface is anisotropic and independent of the supersaturation and preferentially on the active sites of the (100) edge. Moreover, this information is of significance for the improvement of the quality of boric acid recovered from brines and minerals and the synthesis of nanostructures and microstructures of boron-based materials.
ABSTRACT
Large molecular aggregates with sizes ranging from subnanometers to microns are ubiquitous. As atmospheric aerosols they influence our climate, in interstellar space they are discussed as reactive sites, and in medicine small particles are considered as promising candidates to achieve a targeted drug delivery. The present contribution is focused on the characterization of the physical-chemical properties of these particles and on their targeted generation. One of the greatest challenges is to understand the properties of these aggregates on a molecular level. The latter point is discussed in detail focussing on the vibrational dynamics of these particles.