Insights over titanium modified FeMgOx catalysts for selective catalytic reduction of NOx with NH3: Influence of precursors and crystalline structures

11Citations
Citations of this article
9Readers
Mendeley users who have this article in their library.

Abstract

Titanium modified FeMgOx catalysts with different precursors were prepared by coprecipitation method with microwave thermal treatment. The iron precursor is a key factor affecting the surface active component. The catalyst using FeSO4 and Mg(NO3 )2 as precursors exhibited enhanced catalytic activity from 225 to 400◦ C, with a maximum NOx conversion of 100%. Iron oxides existed as γ-Fe2 O3 in this catalyst. They exhibited highly enriched surface active oxygen and surface acidity, which were favorable for low-temperature selective catalytic reduction (SCR) reaction. Besides, it showed advantage in surface area, spherical particle distribution and pores connectivity. Amorphous iron-magnesium-titanium mixed oxides were the main phase of the catalysts using Fe(NO3 )3 as a precursor. This catalyst exhibited a narrow T90 of 200/250–350◦ C. Side reactions occurred after 300◦ C producing NOx, which reduced the NOx conversion. The strong acid sites inhibited the side reactions, and thus improved the catalytic performance above 300◦ C. The weak acid sites appeared below 200◦ C, and had a great impact on the low-temperature catalytic performance. Nevertheless, amorphous iron-magnesium-titanium mixed oxides blocked the absorption and activation between NH3 and the surface strong acid sites, which was strengthened on the γ-Fe2 O3 surface.

Cite

CITATION STYLE

APA

Xu, L., Yang, Q., Hu, L., Wang, D., Peng, Y., Shao, Z., … Li, J. (2019). Insights over titanium modified FeMgOx catalysts for selective catalytic reduction of NOx with NH3: Influence of precursors and crystalline structures. Catalysts, 9(6). https://doi.org/10.3390/catal9060560

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free