Designing supported ZnNi catalysts for the removal of oxygen from bio-liquids and aromatics from diesel

This work describes the effect of the support (TiO sub(2), hybrid 2TiO sub(2)-SiO sub(2), SBA-15 and SBA-15 decorated with TiO sub(2) particles) on the catalytic activity of ZnNi catalysts in the gas-phase hydrodeoxygenation (HDO or O-removal) of phenol and the liquid-phase hydrodearomatization (HDA...

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Veröffentlicht in:Green chemistry : an international journal and green chemistry resource : GC 2012-01, Vol.14 (10), p.2759-2770
Hauptverfasser: LORICERA, C. V, CASTANO, P, INFANTES-MOLINA, A, HITA, I, GUTIERREZ, A, ARANDES, J. M, FIERRO, J. L. G, PAWELEC, B
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Sprache:eng
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Zusammenfassung:This work describes the effect of the support (TiO sub(2), hybrid 2TiO sub(2)-SiO sub(2), SBA-15 and SBA-15 decorated with TiO sub(2) particles) on the catalytic activity of ZnNi catalysts in the gas-phase hydrodeoxygenation (HDO or O-removal) of phenol and the liquid-phase hydrodearomatization (HDA) of synthetic diesel. These reactions are representative of the two major challenges of the hydrotreating unit embedded in a sustainable refinery: (i) decreasing oxygen content of bio-oils (produced in the pyrolysis of lignocellulosic biomass); and (ii) decreasing aromatics content in diesel. The fresh and deactivated catalysts were characterized by XRD, N sub(2) adsorption-desorption, TPR, MS/TPD-NH sub(3), XPS, SEM, HRTEM and coke combustion. Under steady-state conditions, the ZnNi catalyst supported on SBA-15 decorated with TiO sub(2) particles displayed the highest activity in the hydrodeoxygenation of phenol (selectivity toward deoxygenated products > 95%) whereas the ZnNi/SBA-15 catalyst displayed the highest activity in the hydrodearomatization of synthetic diesel. It has been shown that dispersion of the active ingredient is favoured on the SBA-15 substrate. The relationship between structure and activity demonstrated that HDO and HDA reactions require optimized metal dispersion and acid function, metal dispersion being more important for HDA than for HDO reactions.
ISSN:1463-9262
1463-9270
DOI:10.1039/c2gc35901d