Journal
APPLIED CATALYSIS A-GENERAL
Volume 361, Issue 1-2, Pages 18-25Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/j.apcata.2009.03.037
Keywords
Catalyst; Hydrodesulfurization; Metal phosphide; Nickel phosphide; Molybdenum phosphide; 4,6-Dimethyldibenzothiophene; Citric acid
Categories
Funding
- Natural Sciences and Engineering Research Council of Canada
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Unsupported monometallic phosphides (MoP and Ni2P), as well as a series of bimetallic nickel molybdenum phosphides (NixMoP), were synthesized with high Surface area by adding citric acid (CA) to precursor metal salt solutions prior to drying, calcination and temperature-programmed reduction (TPR). The resulting MoP and Ni2P catalysts had surface areas of 139 and 216 m(2)/g, respectively. The surface areas of the NixMoP catalysts decreased with increased Ni content and ranged from 121 to 16 m(2)/g. In all cases, the catalyst surface area was greater than that obtained when a conventional preparation procedure was followed that did not use CA. The activity of the catalysts for the hydrodesulfurization (HDS) of a feed containing 3000 ppm 4,6-dimethyldibenzothiophene (4,6-DMDBT) in toluene was measured at 583 K and 3.0 MPa. The resulting catalysts were highly active and among the Studied Ni2P exhibited the highest HDS activity with a conversion of 87.7% at a WHSV of 26 h(-1) and a phosphides, H-2/liquid feed ratio of 625 (v/v). The HDS TOF decreased in the order Ni2P > NixMoP > MoP and for the NixMOP catalyst, the observed TOF increased with Ni content. (C) 2009 Elsevier B.V. All rights reserved.
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