Design of Aerosol Coating Reactors by CFD

Tuesday, October 18, 2011: 10:35 AM
M100 J (Minneapolis Convention Center)
Beat Buesser and Sotiris E. Pratsinis, Department of Mechanical and Process Engineering, ETH Zurich, Zurich, Switzerland

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.

 


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