(220e) In-Situ Coating of Flame-Made TiO2 Nanoparticles by SiO2 | AIChE

(220e) In-Situ Coating of Flame-Made TiO2 Nanoparticles by SiO2

Authors 

Teleki, A. - Presenter, Particle Technology Laboratory, ETH Zurich
Heine, M. C. - Presenter, Particle Technology Laboratory
Akhtar, K. M. - Presenter, Millennium Inorganic Chemicals (a Cristal Company)
Pratsinis, S. E. - Presenter, Swiss Federal Institute of Technology, Particle Technology Laboratory, ETH Zurich


Mostly rutile titania nanoparticles (doped with Al) about 40 nm in diameter made by flame spray pyrolysis (FSP) were coated at considerable production rates, 30 g/h, in-situ with 2 ? 4 nm thick SiO2 films by mixing the freshly-formed TiO2 aerosol with hexamethyldisiloxane (HMDSO) vapor just downstream of the flame. A hollow ring delivering HMDSO vapor (precursor to SiO2) through 16 jets was judiciously positioned in cross-flow above the enclosed flame coating freshly-made Al-doped rutile TiO2 particles. The as-prepared powders were characterized by (scanning) transmission electron microscopy (STEM and TEM), energy dispersive X-ray analysis, X-ray diffraction, DC plasma optical emission spectroscopy (DCP-OES) and nitrogen adsorption. The coating quality was assessed further in the photocatalytic oxidation of isopropanol to acetone. The coating thickness was controlled by the silica content. The particles were encapsulated by smooth and homogeneous coatings at above 10 wt% SiO2 contents. Premature or early HMDSO vapor injection resulted in segregated SiO2 and patchy or poorly-coated TiO2 particles. The anatase promotion of silica in TiO2 was significantly reduced as the distance of HMDSO vapor injection point from the FSP burner was increased. Well-coated TiO2 particles exhibited limited IPA photooxidation. In contrast, spraying and combusting equivalent mixtures of Si/Al/Ti precursors in the enclosed FSP reactor (without delivering HMDSO through the hollow ring) resulted in particles segregated in amorphous (SiO2) and crystalline (TiO2) domains and thus high photocatalytic activity.