Catalytic elimination of toxic nitrile waste gas is of great significance for preserving the atmospheric environment, but achieving resource utilization during its destruction has been less explored. Herein, this study proposed a universal strategy for nitrile waste gas purification and NH3 generation simultaneously. The developed silver single-atom-doped ceria nanorod (Ag1/R-CeO2) was endowed with near complete mineralization and around 90% NH3 yield at 300-350 °C for the catalytic oxidation of both acetonitrile and acrylonitrile. The introduction of the Ag single atom created more surface oxygen vacancies, thereby promoting water activation to form abundant surface hydroxyl groups. As a benefit from this, the hydrolysis reaction of nitrile to generate NH3 was accelerated. Meanwhile, the electron transfer effect from the Ag atom to Ce and hydroxyl species facilitated NH3 desorption, which inhibited the oxidation of NH3. Moreover, the increased surface oxygen vacancies also promoted the mineralization of hydrolysis carbonaceous intermediates to CO2. In contrast, the Ag nanoparticle-modified sample possessed stronger reducibility and NH3 adsorption, leading to the excessive oxidation of NH3 to N2 and NOx. This work provided a useful guidance for resourceful purification of nitrile waste gas.
Keywords: Ag single atom; CeO2 nanorods; NH3 generation; catalytic elimination; nitrile waste gas.