Wj. Stark et al., Flame aerosol synthesis of vanadia-titania nanoparticles: Structural and catalytic properties in the selective catalytic reduction of NO by NH3, J CATALYSIS, 197(1), 2001, pp. 182-191
Flame aerosol synthesis has been used to prepare vanadia-titania nanopartic
les with high activity for the selective catalytic reduction of NO by NH3.
The mixed oxides were prepared from vanadium and titanium alkoxides which w
ere evaporated into an argon stream and burned in a methane oxygen diffusio
n flame. Silica-containing samples were produced in a similar way by mixing
hexamethyldisiloxane vapor into the precursor stream. Different flame stru
ctures were investigated for the effect of temperature and residence time o
n particle morphology, vanadia surface species, and overall catalytic activ
ity. By changing the oxygen flow rate into the flame, particles with specif
ic surface areas between 23 and 120 m(2)/g could be produced. High-resoluti
on transmission electron microscopy (HRTEM) revealed that nanoparticles wer
e spherical with diameters of 10 to 50 nm. X-ray photoelectron spectroscopy
analysis indicated that vanadia was dispersed on the surface of the titani
a spheres. No indication for the presence of crystalline V2O5 could be foun
d by X-ray diffraction or HRTEM. Catalysts with a vanadia surface loading o
f 10 mu mol/m(2) showed high activity with less than 1% N2O formation up to
350 degreesC. Catalytic activity strongly depended on the vanadia loading;
an increase from 2.5 to 7 mu mol/m(2) resulted in a 30 times higher activi
ty per vanadium. Addition of silica lowered the overall activity but did no
t change the activation energy. Raman spectroscopy indicated the presence o
f vanadate clusters. Temperature-programmed reduction corroborated that no
significant amount of vanadia entered the titania lattice to form an inters
titial solution. The selective catalytic reduction activity of as-prepared
vanadia-titania is comparable to the best catalysts obtained by wet chemica
l methods. (C) 2001 Academic Press.