Abstract

A series of M-AlOx mixed oxides (M = Cu, Co, Ni) with the addition of high loadings of rare earth elements (REE, R = Ce, Nd, Pr; R0.5M0.8Al0.2, molar ratio) were investigated in N2O decomposition. The precursors were prepared by coprecipitation and subsequent calcination at 600 °C. The obtained mixed metal oxides were characterized by X-ray diffraction with Rietveld analysis, N2 sorption, and H2 temperature-programmed reduction. Depending on the nature of REE and the initial M-Al system, R cations could be separately segregated in oxide form or coordinated with the transition metal cations and form mixed structures. The addition of Ce3+ consistently led to nanocrystalline CeO2 mixed with the divalent oxides, whereas the addition of Nd3+ or Pr3+ resulted in the formation of their respective oxide phases as well as perovskites/Ruddlesden–Popper phases. The presence of REE modified the textural and redox properties of the calcined materials. The rare earth element-induced formation of low-temperature reducible MOx species that systematically improved the N2O decomposition on the modified catalysts compared to the pristine M-Al materials by the order of Co > Ni > Cu. The Ce0.5Co0.8Al0.2 catalyst revealed the highest activity and remained stable (approximately 90% of N2O conversion) for 50 h during time-on-stream in 1000 ppm N2O, 200 ppm NO, 20 000 ppm O2, 2500 ppm H2O/N2 balance at WHSV = 16 L g−1 h−1.

Highlights

  • Nitrous oxide (N2O), an inevitable by-product from adipic and nitric acid production plants, is a recognized global warming agent and contributes to the degradation of the stratospheric ozone layer

  • The obtained mixed metal oxides were characterized by X-ray diffraction with Rietveld analysis, N2 sorption, and H2 temperature-programmed reduction

  • Kannan reported that CuAl, NiAl, and CoAl mixed oxides derived from respective HT showed activity in decomposition of N2O (deN2O) by using 0.1 g of catalyst, 0.0985 vol % N2O/He, a total flow rate of 100 cm3 min-1, 450 °C [7]

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Summary

Introduction

Nitrous oxide (N2O), an inevitable by-product from adipic and nitric acid production plants, is a recognized global warming agent and contributes to the degradation of the stratospheric ozone layer. The oxides formed in the absence of REE present quite different distributions of Sample code Crystalline phases a Specific surface area / m2 g-1 Pore volume / cm3 g-1 Mesopore size / nmd CeCuAl NdCuAl PrCuAl NiAl

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