2 research outputs found
Ambient Temperature Hydrocarbon Selective Catalytic Reduction of NO<sub><i>x</i></sub> Using Atmospheric Pressure Nonthermal Plasma Activation of a Ag/Al<sub>2</sub>O<sub>3</sub> Catalyst
Atmospheric pressure nonthermal-plasma-activated
catalysis for
the removal of NO<sub><i>x</i></sub> using hydrocarbon selective
catalytic reduction has been studied utilizing toluene and <i>n</i>-octane as the hydrocarbon reductant. When the plasma was
combined with a Ag/Al<sub>2</sub>O<sub>3</sub> catalyst, a strong
enhancement in activity was observed when compared with conventional
thermal activation with high conversions of both NO<sub><i>x</i></sub> and hydrocarbons obtained at temperature ≤250 °C,
where the silver catalyst is normally inactive. Importantly, even
in the absence of an external heat source, significant activity was
obtained. This low temperature activity provides the basis for applying
nonthermal plasmas to activate emission control catalysts during cold
start conditions, which remains an important issue for mobile and
stationary applications
Redispersion of Gold Supported on Oxides
Although many gold heterogeneous catalysts have been
shown to exhibit
significant activity and high selectivity for a wide range of reactions
in both the liquid and gas phases, they are prone to irreversible
deactivation. This is often associated with sintering or loss of the
interaction of the gold with the support. Herein, we report on the
use of methyl iodide as a method of dispersing gold nanoparticles
supported on silica, titania, and alumina supports. In the case of
titania- and alumina-based catalysts, the gold was transformed from
nanometer particles into small clusters and some atomically dispersed
gold. In contrast, although there was a drop in the gold particle
size on the silica support following CH<sub>3</sub>I treatment, the
size remained in the submicrometer range. The structural changes were
correlated with changes in the selectivity and activity for ethanol
dehydration and benzyl alcohol oxidation. From these observations,
it is clear that this treatment provides a method by which deactivated
gold catalysts can be reactivated via redispersion of the gold