The
electrolytic aluminum waste contains harmful components, such
as fluorides. Sending it to coal-fired boilers seems to be a prospective
scheme to achieve the harmless treatment of waste. However, the negative
influence of F on the SCR catalyst should be examined. In this study,
a fixed-bed reactor system is built up to study the deactivation of
the V2O5–WO3–TiO2 SCR catalyst by HF when the electrolytic aluminum waste is
co-fired with coal in boilers. The activity of the catalyst is evaluated
by the NH3-SCR reaction. The deactivation mechanism is
investigated through tests of NH3 temperature-programmed
desorption, H2 temperature-programmed reduction, X-ray
diffraction, X-ray photoelectron spectroscopy, Brunauer–Emmett–Teller
(BET), in situ diffuse reflectance infrared Fourier transform spectroscopy,
and Raman spectroscopy. The results show that for deactivated catalyst
samples, the SCR catalytic activity drops obviously, especially when
they work at lower temperatures. Although HF could enhance Brønsted
acid sites, increase the Oα (adsorbed oxygen) concentration,
and facilitate the Lewis acid site formation, it would not compensate
for decreases of V5+ on the catalyst surface and BET surface
area, which results in an activity reduction of the catalyst sample.