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Direct catalytic decomposition of N2O over Co(x)/RPSA catalysts

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As one of the main greenhouse gases, reducing emissions of N2O is imperative, for which catalytic decomposition is one of the most effective methods. A series of cobalt catalysts supported… Click to show full abstract

As one of the main greenhouse gases, reducing emissions of N2O is imperative, for which catalytic decomposition is one of the most effective methods. A series of cobalt catalysts supported on RPSA zeolite, denoted as Co(x)/RPSA-T, were prepared using the impregnation method and characterized by X-ray diffraction (XRD) analysis, Brunauer–Emmett–Teller (BET) measurements, thermogravimetric mass spectrometry (TG–MS), H2 temperature-programmed reduction (TPR), NH3 temperature-programmed desorption (TPD), X-ray photoelectron spectroscopy (XPS), X-ray fluorescence (XRF) spectroscopy, and in situ diffuse reflectance infrared Fourier-transform spectroscopy (DRIFTS). Catalytic activity tests for N2O decomposition were carried out in a fixed-bed microreactor. The results showed that the redox properties of the catalysts remarkably influenced their catalytic performance. The catalytic activity results for the Co(10)/RPSA-600 catalyst showed the best performance under the conditions of 0.65 vol% N2O, 0.88 vol% O2, with Ar as balance gas, achieving conversions of 10 % and 90 % of N2O at temperature of 348 °C and 438 °C, respectively.

Keywords: direct catalytic; catalytic decomposition; decomposition n2o; rpsa; spectroscopy; decomposition

Journal Title: Research on Chemical Intermediates
Year Published: 2019

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