The effect of surface characteristics on the interaction between nanoparticles and their agglomeration in dense gas suspensions is still not fully understood. It is known that when the surface is covered with hydroxyl groups, the interaction between nanoparticles becomes substantially stronger than in the absence of these groups; this strengthening is typically attributed to the formation of capillary bridges between the particles. However, this work shows that part of the increase of the interaction is due to the direct hydrogen bonds formed between the surfaces of the polar particles. Dry nitrogen was used to fluidize polar (hydrophilic) and apolar (hydrophobic) SiO2, TiO2 and Al2O3 particles, with a size ranging from 13 to 21 nm. The dry polar particles showed smaller bed expansion and larger minimum fluidization velocity compared to their apolar counterparts, indicating stronger interparticle forces. The results show the importance of including the formation of hydrogen bonds in the modeling of the interaction between dry and polar nanoparticles.
In this paper, the authors demonstrate a novel spatial atomic layer deposition (ALD) process based on pneumatic transport of nanoparticle agglomerates. Nanoclusters of platinum (Pt) of $1 nm diameter are deposited onto titania (TiO 2 ) P25 nanoparticles resulting to a continuous production of an active photocatalyst (0.12-0.31 wt. % of Pt) at a rate of about 1 g min À1 . Tuning the precursor injection velocity (10-40 m s À1 ) enhances the contact between the precursor and the pneumatically transported support flows. Decreasing the chemisorption temperature (from 250 to 100 C) results in more uniform distribution of the Pt nanoclusters as it decreases the reaction rate as compared to the rate of diffusion into the nanoparticle agglomerates. Utilizing this photocatalyst in the oxidation reaction of Acid Blue 9 showed a factor of five increase of the photocatalytic activity compared to the native P25 nanoparticles. The use of spatial particle ALD can be further expanded to deposition of nanoclusters on porous, micron-sized particles and to the production of core-shell nanoparticles enabling the robust and scalable manufacturing of nanostructured powders for catalysis and other applications.
Molecular layer deposition (MLD) was used to coat micron-sized protein particles in a fluidized bed reactor. Our results show that the dissolution rate of particles coated via MLD rapidly decreases with the increase in number of coating cycles, while the uncoated particles dissolve instantaneously.
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