Title

Effect of calcination temperature on steam reforming activity of Ni-based pyrochlore catalysts

Document Type

Article

Publication Date

7-1-2020

Abstract

This work served as the second part of a study evaluating the effect of calcination temperature (700–1000 °C) on Ni-based lanthanum zirconate pyrochlore catalysts for methane steam reforming. A previous study (Haynes et al. Ceram. Int. 2017 (43) 16744) provided a thorough characterization of the material properties for the catalysts used here, and this study focuses on the evaluation of catalytic activity. The activity was assessed by two different experimental studies: the effect of reaction temperature using a temperature programmed surface reaction (TPSR), and the effect of reaction pressure. The results demonstrate a complex interaction between the Ni particles and surface LaO species under the methane steam reforming conditions. Specifically, the material calcined at the lowest temperature (700 °C) possesses the highest activity and selectivity, which is attributed to smaller and more well-dispersed Ni particles on the surface, and, more importantly, a lesser degree La enrichment at the surface. All catalysts were deactivated by steam to NiO under all conditions tested, but at certain low reaction pressure (p = 0.23 MPa) conditions the materials calcined at 700–900 °C are able to completely recover equilibrium activity in-situ that is then robust and stable under both low and high reaction pressures (p = 1.8 MPa) suggesting the formation of a synergistic relationship between Ni and La for syngas production. However, exposure of a fresh material to high reaction pressures leads to a rapid and irreversible loss in both CH conversion and syngas selectivity whether in the fresh (no pretreatment), or pretreated (steam, H or Ar only at 800 °C) form for any catalyst. The mechanism for deactivation appears to be due to the presence of LaO species that become mobile, possibly by the formation of La–OH, and covers the active Ni particles and inhibits sites responsible for the CH decomposition. x 4 2 x 4

Publication Source (Journal or Book title)

Journal of Rare Earths

First Page

711

Last Page

718

This document is currently not available here.

COinS