2018 AIChE Annual Meeting
(552c) Structures and Dynamics of Boehmite Crystal Aggregation
Authors
Jaehun Chun - Presenter, Pacific Northwest National Laboratory
Elias Nakouzi, Pacific Northwest National Laboratory
Jennifer Soltis, Pacific Northwest National Laboratory
Benjamin Legg, Pacific Northwest National Laboratory
Gregory K. Schenter, Pacific Northwest National Laboratory
Xin Zhang, Pacific Northwest National Laboratory
Trent R. Graham, Voiland School of Chemical Engineering and Bioengineering, Washington State University
Kevin Rosso, Pacific Northwest National Laboratory
Lawrence Anovitz, Oak Ridge National Laboratory
James J. De Yoreo, Pacific Northwest National Laboratory
While aggregation kinetics and resultant aggregate structures for spherical colloids have been studied extensively, such studies for sharp-edged non-spherical particles have been relatively unexplored. We studied the structure and dynamics of aggregation for rhombohedral boehmite crystals as a function of solution pH and ionic strength based on dynamic light scattering (DLS), combined with cryo-transmission electron microscope. The coagulation rate constants obtained from DLS during the early stages of aggregation are found to span seven orders of magnitude and cross both the reaction-limited and diffusion-limited regimes. A simple scaling for van der Waals, electrostatic, and hydrodynamic interactions combined with rotational/translational diffusivities of irregular particle shapes provides qualitative understanding of the effects of orientation for the irregular-shaped colloids on the early stages of aggregation. Unusually high fractal dimensions of the aggregates are observed in the diffusion-limited aggregation regime, which can be qualitatively explained by a simple geometric parameter (i.e., a contact area between the particles) based on Monte Carlo simulations.