Heterogeneous catalysts for the low temperature NH3-SCR of NOx can be strongly deactivated due to the accumulation of specific compounds deriving from an upstream desulphurization unit, such as a Sea Water Scrubber. In this work, we set out to investigate the specific role of K+ and of its counter-ion (Cl- or NO3-) on the combined poisoning effect induced on the catalytic features of a MnOx/ TiO2 system. Poisoning of the catalyst was performed ex-situ by impregnation with two target loadings of each K salt, followed by a mild thermal treatment at 250 °C, corresponding to the maximum operating temperature of the SCR system. Fresh and poisoned catalysts were characterized by means of ICP-MS, BET, H2-TPR, NH3-Adsorption, NH3-Temperature Programmed Desorption-Reaction and in-situ DRIFT and the impact of poisoning was assessed and compared for the NH3-SCR of NO as well as for the NH3-SCO (Selective Catalytic Oxidation) reaction
Combined poisoning effect of K+ and its counter-ion (Cl- or NO3-) on MnOx/TiO2 catalyst during the low temperature NH3-SCR of NO
Cimino Stefano;Totarella Giorgio;Tortorelli Miriam;Lisi Luciana
2017
Abstract
Heterogeneous catalysts for the low temperature NH3-SCR of NOx can be strongly deactivated due to the accumulation of specific compounds deriving from an upstream desulphurization unit, such as a Sea Water Scrubber. In this work, we set out to investigate the specific role of K+ and of its counter-ion (Cl- or NO3-) on the combined poisoning effect induced on the catalytic features of a MnOx/ TiO2 system. Poisoning of the catalyst was performed ex-situ by impregnation with two target loadings of each K salt, followed by a mild thermal treatment at 250 °C, corresponding to the maximum operating temperature of the SCR system. Fresh and poisoned catalysts were characterized by means of ICP-MS, BET, H2-TPR, NH3-Adsorption, NH3-Temperature Programmed Desorption-Reaction and in-situ DRIFT and the impact of poisoning was assessed and compared for the NH3-SCR of NO as well as for the NH3-SCO (Selective Catalytic Oxidation) reactionI documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.