posted on 2019-12-26, 22:30authored byJie Zeng, Xuemei Zhong, Jie Yu, Tao Zhang, Yazhou Wang, Huazhen Chang
In this study, a series of CoCeOx catalysts
were prepared by template, solid-state grinding with cobalt sulfate
or cobalt acetate as the precursor and the oil bath method for catalytic
reduction of NOx by CO (CO–NO).
These catalysts were characterized by X-ray diffraction, Brunauer–Emmett–Teller,
Raman spectroscopy, X-ray photoelectron spectroscopy, temperature-programmed
reduction of H2, and in situ diffuse reflectance infrared
Fourier transform spectroscopy (DRIFTS). The results indicated that
CoCeOx-TA and CoCeOx-SS catalysts exhibited much higher activity, which were attributed
to excellent reducibility property, abundant chemical adsorbed oxygen,
and NO absorption sites. In the presence of O2, the activity
decreased obviously over CoCeOx-TA, CoCeOx-SS, and CoCeOx-SA catalysts. However, the activity increased at high temperatures
over the CoCeOx-OA catalyst. According
to the result of in situ DRIFTS, nitrate species decreased over CoCeOx-TA, CoCeOx-SS,
and CoCeOx-SA catalysts in the presence
of O2, which might inhibit the reduction efficiency of
NO. Moreover, NO adsorption was not affected by O2 over
CoCeOx-OA catalyst, which could contribute
to its high activity in the CO-selective catalytic reduction reaction.