Anomalous Sinking of Spheres due to Local Fluidization of Apparently Fixed Powder Beds.

The sinking of an intruder sphere into a powder bed in the apparently fixed bed regime exhibits complex behavior in the sinking rate and the final depth when the sphere density is close to the powder bed density. Evidence is adduced that the intruder sphere locally fluidizes the apparently fixed powder bed, allowing the formation of voids and percolation bubbles that facilitates spheres to sink slower but deeper than expected. By adjusting the air injection rate and the sphere-to-powder bed density ratio, this phenomenon provides the basis of a sensitive large particle separation mechanism.

Impacts of compression on crystallization behavior of freeze-dried amorphous sucrose.

An amorphous matrix comprised of sugar molecules is used as excipient and stabilizing agent for labile ingredients in the pharmaceutical industry. The amorphous sugar matrix is often compressed into a tablet form to reduce the volume and improve handling. Herein, the effect of compression on the crystallization behavior of an amorphous sucrose matrix was investigated. Amorphous sucrose samples were prepared by freeze-drying and compressed under different conditions, followed by analyses by differential scanning calorimetry, isothermal crystallization tests, X-ray powder diffractometry, Fourier transform infrared spectroscopy (FTIR), and gas pycnometry. The compressed sample had a lower crystallization temperature and a shorter induction period for isothermal crystallization, indicating that compression facilitates the formation of the critical nucleus of a sucrose crystal. Based on FTIR and molecular dynamics simulation results, the conformational distortion of sucrose molecules due to the compression appears to contribute to the increase in the free energy of the system, which leads to the facilitation of critical nucleus formation. An isothermal crystallization test indicated an increase in the growth rate of sucrose crystals by the compression. This can be attributed to the transformation of the microstructure from porous to nonporous, as the result of compression.

Difference in screening effect of alkali metal counterions on H-AOT-based W/O microemulsion formation.

The purpose of this study was to estimate the screening of electrostatic repulsions between the polar headgroups of AOT(-) by alkali metal counterions and to explore the relationships between the screening effect and the phase behavior of H-AOT-based W/O microemulsions. The screening effect was evaluated by means of critical micelle concentration (CMC) data using the pyrene 1:3 ratio method with aqueous solutions containing M-AOT (where M(+) = Li(+), Na(+), K(+), Rb(+) and Cs(+)) to form normal micelles, and by counterion binding constants, determined from plots of CMC versus counterion concentration. The order of the screening effect was found to be K(+) approximately = Rb(+) > Cs(+) > Na(+) > Li(+). Interestingly, the order does not follow the hydration size dependence of the alkali metal counterions. An aqueous MOH solution containing a given concentration/H-AOT/isooctane was emulsified at a water content (w(0) = [water]/[H-AOT]) of 10 to produce H-AOT-based W/O microemulsions. The phase behavior and size variation were investigated by FT-IR and DLS measurements. The emulsified mixture separates into two phases at lower MOH concentration due to an insufficient screening effect. When the concentration is increased to a level sufficient to intensify the screening effect, W/O microemulsions are formed without phase separation at lower KOH and RbOH concentrations compared to CsOH. A period of standing after the emulsification and a higher concentration of NaOH compared to KOH, RbOH, and CsOH are required to form W/O microemulsions. W/O microemulsions are not formed in the case of LiOH. These results indicate that the formation of a W/O microemulsion with H-AOT is strongly correlated with the order of the screening effect. A possible cause for the difference in the screening effect is proposed based on hydration of the polar headgroups and counterions, as evidenced by FT-IR spectral data, i.e., symmetrical sulfonate stretching and O-H stretching.