The catalytic activities of moderately activated
pitch-based carbon fibers (ACFs) were examined for the
reduction of low concentration NO (10 ppm) with ammonia in dry and wet
(80% humidity) air. A particular
ACF calcined at 850 °C exhibited very high activity even in wet air,
providing stationary NO conversions
of 76 and 46% in dry and wet air, respectively, at the contact time
W/F = 5 × 10-3 g
min mL-1. An optimum
NH3 concentration of 15 ppm gave the largest NO conversion
and the lowest leakage. The adsorptive
abilities of the ACFs for NO and NH3 do not directly
correlate with their catalytic activity, indicating that
all adsorbed species are not active for the reduction. Catalytic
activity was enhanced by calcination in
an inert atmosphere, while reduced adsorptive ability suggests that the
unsaturated carbon valencies
induced by the elimination of oxygen functional groups act as
additional active sites over the ACF surface.
The hydrophobic nature, which is also enhanced by the calcination,
is essential in moderating the retardation
by H2O of both NO adsorption and activation. The
moderately activated ACFs of 700−800 m2/g
surface
area after the heat treatment at 800−850 °C appear to contain the
active sites of highest activity situated
on the hydrophobic surface within pores not occupied by condensed
H2O.