Role of the ru and support in sulfided RuNiMo catalysts in simultaneous hydrodearomatization (HDA), hydrodesulfurization (HDS), and Hydrodenitrogenation (HDN) reactions

B. Pawelec, R. M. Navarro, P. Castaño, M. C. Álvarez-Galván, J. L.G. Fierro

Research output: Chapter in Book/Report/Conference proceedingConference contribution

14 Scopus citations

Abstract

Simultaneous hydrodesulfurization (HDS), hydrodearomatization (HDA), and hydrodenitrogenation (HDN) reactions have been studied over sulfided RuNiMo/Al2O3 catalysts. The effects of Ru promotion and alumina support modification with HY zeolite and P on catalyst performance have been studied using a synthetic feed containing dibenzothiophene, toluene, naphthalene, and pyridine. Activity tests were carried out in a semiautomatic microplant equipped with a continuous flow reactor, working under conditions similar to industrial practice (P ) 5 MPa, T ) 285-360 °C, and liquid hourly space velocity (LHSV) ) 3 and 4.5 h-1). The catalysts were characterized by SBET, X-ray diffraction (XRD), temperature-programmed reduction (TPR), temperature-programmed desorption of ammonia (TPD-NH3), and X-ray photoelectron spectroscopy (XPS) techniques. Activity tests revealed that optimal Ru loading is 1 wt % (nominal). Under fixed experimental conditions (300 °C, 5 MPa, and LHSV ) 3 h-1), ultra-low sulfur diesel (S < 20 ppm S) was obtained over a Ru(1%)Ni(5%)Mo(14%)/?-Al2O3 catalyst from a feed containing 18361 ppm S. However, this catalyst showed similar capability toward aromatics and pyridine removal as a commercial NiMo/Al2O3 catalyst. At a reaction temperature of 345 °C, the 5% HY-Al2O3 substrate led to a small increase in the hydrogenation capability of this catalyst but without enhancement of its HDS/HDN capability. On the contrary, the P-modified substrate resulted in a lower activity. The properties of the supported catalysts are discussed in terms of the support effect and Ru promotion. © 2009 American Chemical Society.
Original languageEnglish (US)
Title of host publicationEnergy and Fuels
DOIs
StatePublished - Mar 19 2009
Externally publishedYes

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