Perovskite-Based Catalysts as Efficient, Durable, and Economical NO<sub>x</sub> Storage and Reduction Systems

oleh: Jon A. Onrubia-Calvo, Beñat Pereda-Ayo, Juan R. González-Velasco

Format: Article
Diterbitkan: MDPI AG 2020-02-01

Deskripsi

Diesel engines operate under net oxidizing environment favoring lower fuel consumption and CO<sub>2</sub> emissions than stoichiometric gasoline engines. However, NO<sub>x</sub> reduction and soot removal is still a technological challenge under such oxygen-rich conditions. Currently, NO<sub>x</sub> storage and reduction (NSR), also known as lean NO<sub>x</sub> trap (LNT), selective catalytic reduction (SCR), and hybrid NSR&#8722;SCR technologies are considered the most efficient control after treatment systems to remove NO<sub>x</sub> emission in diesel engines. However, NSR formulation requires high platinum group metals (PGMs) loads to achieve high NO<sub>x</sub> removal efficiency. This requisite increases the cost and reduces the hydrothermal stability of the catalyst. Recently, perovskites-type oxides (ABO<sub>3</sub>) have gained special attention as an efficient, economical, and thermally more stable alternative to PGM-based formulations in heterogeneous catalysis. Herein, this paper overviews the potential of perovskite-based formulations to reduce NO<sub>x</sub> from diesel engine exhaust gases throughout single-NSR and combined NSR&#8722;SCR technologies. In detail, the effect of the synthesis method and chemical composition over NO-to-NO<sub>2</sub> conversion, NO<sub>x</sub> storage capacity, and NO<sub>x</sub> reduction efficiency is addressed. Furthermore, the NO<sub>x</sub> removal efficiency of optimal developed formulations is compared with respect to the current NSR model catalyst (1&#8722;1.5 wt % Pt&#8722;10&#8722;15 wt % BaO/Al<sub>2</sub>O<sub>3</sub>) in the absence and presence of SO<sub>2</sub> and H<sub>2</sub>O in the feed stream, as occurs in the real automotive application. Main conclusions are finally summarized and future challenges highlighted.