2011 Annual Meeting

(223f) Design of Aerosol Coating Reactors by CFD

Authors

Pratsinis, S. E. - Presenter, Swiss Federal Institute of Technology, Particle Technology Laboratory, ETH Zurich


Core-shell particles facilitate incorporation of functional particles into
host (e.g. liquid or polymer) matrices like silica-coated TiO2
pigments1, carbon coated Cu for sensors2 or superparamagnetic3 Fe2O3. Typically
core-shell particles are made in the liquid phase4 but there is keen interest to
develop gas-phase or aerosol coating processes that do not generate liquid
by-products, offer fewer process steps, easier particle collection and hermetic3 shells. Coating of particles in the
gas phase, however, is challenging, as particle motion and growth are much
faster than in liquids. As a result, it is difficult to control and develop a
scalable gas phase coating process. So, even commercially produced particles
made by aerosol routes (e.g. pigmentary TiO2 made by the ?chloride?
process) are coated by wet processes4.

Here5, gas-phase (aerosol) coating is
elucidated in considerable detail, for the first time to our knowledge, by
computational fluid and particle dynamics for core particles (TiO2)
and coating shells (SiO2). Emphasis is placed on understanding the
influence of process variables (coating weight fraction and mixing intensity
(Figure 1) and geometry of core aerosol & shell precursor vapor) on
core-shell product characteristics by a trimodal aerosol particle dynamics
model6 accounting for SiO2 monomer
generation, coagulation and sintering. The predicted extent of complete (or
hermetic) coating shells is compared to the measured photocatalytic oxidation
of isopropanol by such particles7,8 and release of acetone. As hermetic SiO2
shells prevent the photocatalytic activity of TiO2, the performance
of coated particles is explained by the spatial distribution of shell thickness
on core particles with detailed reactor flow field analysis.

Financial support from the Swiss National Science Foundation (SNF) grant #
200021-119946/1 and European Research Council is gratefully acknowledged.

Figure 1 Influence of nitrogen
flow rate (mixing intensity) a) 5.8 l/min, b) 15.8 l/min and c) 30.8 l/min on
the coating precursor and coating shell thickness distribution inside the
aerosol coating reactor.

1.        
Subramanian NS, Diemer RB, Gai PL; E. I. du Pont de Nemours and Company
(Wilmington, DE, US); Process for making durable rutile titanium dioxide
pigment by vapor phase deposition of surface treatment. US patent
200627303(A1). 2006.

2.        
Athanassiou EK, Grass RN, Stark WJ. Large-scale production of carbon-coated
copper nanoparticles for sensor applications. Nanotechnology. 2006; 17,
(6), 1668-1673.

3.        
Teleki A, Suter M, Kidambi PR, Ergeneman O, Krumeich F, Nelson BJ, Pratsinis
SE. Hermetically coated superparamagnetic Fe2O3 particles
with SiO2 nanofilms. Chem. Mater. 2009; 21, (10), 2094-2100.

4.        
Egerton TA. The modification of fine powders by inorganic coatings. KONA. 1998;
16, 46-59.

5.        
Buesser B, Pratsinis SE. Design of gas-phase synthesis of core-shell particles
by computational fluid ? aerosol cynamics. AIChE J. 2011; DOI: 10.1002/aic.12512,

6.        
Buesser B, Pratsinis SE. Design of Aerosol Particle Coating: Thickness, Texture
and Efficiency. Chem. Eng. Sci. 2010; in Press, doi:
10.1016/j.ces.2010.07.011,

7.        
Teleki A, Heine MC, Krumeich F, Akhtar MK, Pratsinis SE. In-situ coating
of flame-made TiO2 particles by nanothin SiO2 films. Langmuir.
2008; 24, (21), 12553-12558.

8.        
Teleki A, Buesser B, Heine MC, Krumeich F, Akhtar MK, Pratsinis SE. Role of
gas-aerosol mixing during in situ coating of flame-made titania particles. Ind. Eng. Chem. Res. 2009; 48, (1), 85-92.