Volume 50 Issue 8
Aug.  2022
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ZHANG Heng, ZHOU Hao, WEN Ni-ni, WANG Xu-rui, XU Lu, SU Ya-xin. Selective catalytic reduction of nitric oxide with propylene over one-step synthesized Cu-SAPO-44 catalysts[J]. Journal of Fuel Chemistry and Technology, 2022, 50(8): 1064-1074. doi: 10.19906/j.cnki.JFCT.2022012
Citation: ZHANG Heng, ZHOU Hao, WEN Ni-ni, WANG Xu-rui, XU Lu, SU Ya-xin. Selective catalytic reduction of nitric oxide with propylene over one-step synthesized Cu-SAPO-44 catalysts[J]. Journal of Fuel Chemistry and Technology, 2022, 50(8): 1064-1074. doi: 10.19906/j.cnki.JFCT.2022012

Selective catalytic reduction of nitric oxide with propylene over one-step synthesized Cu-SAPO-44 catalysts

doi: 10.19906/j.cnki.JFCT.2022012
Funds:  The project was supported by Natural Science Foundation of Jiangsu Province (BK20181161), National Natural Science Foundation of China (51278095), Jiangsu 333 Engineering Research Project (2018) and Jiangsu Provincial Excellent Science and Technology Innovation Team (2019).
  • Received Date: 2021-12-31
  • Accepted Date: 2022-02-18
  • Rev Recd Date: 2022-02-11
  • Available Online: 2022-02-25
  • Publish Date: 2022-08-26
  • Cu-SAPO-44 zeolite catalysts were synthesized by one-step hydrothermal method using cyclohexylamine (CHA) and Cu-amine complex (Cu-TEPA) as co-template. They were used for selective catalytic reduction of nitric oxide with propylene (C3H6-SCR) under lean burning condition. These catalysts were characterized by N2 adsorption-desorption, X-ray diffraction (XRD), transmission electron microscopy (TEM), UV-vis spectroscopy (UV-vis), NH3 temperature-programmed desorption (NH3-TPD) and H2 temperature-programmed reduction (H2-TPR). Compared with pure SAPO-44, the introduction of Cu-TEPA significantly enhanced the catalytic activity of C3H6-SCR. When Cu/Al was 0.25, Cu-SAPO-44 catalyst had the largest specific surface area, abundant acidic sites and moderate isolated Cu2+ species, thus it had the best deNOx performance. With the increase of Cu-TEPA introduction, copper species would aggregate on the surface of the zeolite and form more inactive CuO, thus reducing the denitrification activity. In situ study by DRIFTS indicated that isolated Cu2+ could contribute to the adsorption and activation of NO and C3H6, thus enhancing in the formation of −NCO, which was a key intermediate of the reaction. The Cu-SAPO-44 catalyst maintained more than 60% NOx conversion and more than 90% N2 selectivity in long term test of 50 h, showing appropriate reaction stability.
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