(673h) Water Induced Ammonia Production on CuO/Al2O3 Catalyst in NO + CO Reaction | AIChE

(673h) Water Induced Ammonia Production on CuO/Al2O3 Catalyst in NO + CO Reaction

Authors 

Liu, F. - Presenter, University of Central Florida
Tan, W., University of Central Florida
Xie, S., University of Central Florida
Dong, L., Nanjing University
Based on our prior knowledge that CuO based catalysts exhibited superior catalytic performance in NO reduction by CO [1], CuO/Al2O3 serial catalysts with different CuO loadings (x wt.% CuO/Al2O3, denoted as xCu/Al) were synthesized using incipient wetness impregnation (IWI) method and evaluated for the possible NH3 production from NO, CO and H2O. With the increase of CuO loadings from 1 to 12 wt.%, monotonically increased NO removal efficiency was achieved on xCu/Al catalysts under dry condition (Fig. 1a). However, when 5 vol.% H2O was added to the feeding stream, the NO conversion on 5Cu/Al increased significantly, achieving almost the same level as that on 12Cu/Al (Fig. 1b). Abundant NH3 was formed on xCu/Al catalysts with the addition of H2O to the feeding stream (Fig. 1c and 1d). The NH3 generation on 5Cu/Al was the most vigorous, which started at the lowest temperature (275 oC). The efficient conversion of NO to NH3 and the possible reaction between NH3 and NO should be the main reason for the noticeable enhancement of NO reduction efficiency on 5Cu/Al in the presence of H2O. Unlike that isolated Cu ions or crystalline CuO particles were formed on CuO/Al2O3 catalysts with lower (≤ 3 wt.%) or higher (≥ 7 wt.%) CuO loadings, respectively, highly dispersed CuOx clusters were formed on 5Cu/Al. The highly dispersed CuOx clusters with superior redox performance could better facilitate the activation/dissociation of H2O to react with NO and CO, forming NH3 and CO2. This work provides a new strategy for NH3 production from two common air pollutants with the assistance of H2O on economic CuO/Al2O3 catalysts under mild reaction conditions.

References:

[1] W. Tan, Y. Cai, S. Xie, J. Xu, K. Ma, K. Ye, L. Ma, S. N. Ehrlich, W. Zou, F. Gao, L. Dong, F. Liu. Chem. Eng. J. 456: 140807, 2023.

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