Catalytic partial oxidation of n-tetradecane using Rh and Sr substituted pyrochlores: Effects of sulfur

• Published in: Catalysis today 2009-07, Vol.145 (1), p.121-126
• Main Authors: Haynes, Daniel J., Berry, David A., Shekhawat, Dushyant, Spivey, James J.
• Format: Article
• Language: English
• Subjects: CARBON; CATALYSTS; Catalytic partial oxidation; Catalytic partial oxidation, Logistic fuel reforming, Pyrochlore, Rhodium, Fuel cell, Fuel processing; DEACTIVATION; ELECTRONS; ENERGY PLANNING, POLICY, AND ECONOMY; Fuel cell; FUEL CELLS; Fuel processing; LANTHANUM; Logistic fuel reforming; OXIDATION; PYROCHLORE; Rhodium; SULFUR; ZIRCONATES
• ISSN: 0920-5861; 1873-4308
• DOI: 10.1016/j.cattod.2008.05.014

The presence of high levels of organosulfur compounds hinders the catalytic partial oxidation (CPOX) of logistic fuels into a H 2-rich gas stream for fuel cells. These species poison traditional supported metal catalysts because the sulfur adsorbs strongly to electron dense metal clusters and promotes the formation of carbon on the surface. To minimize deactivation by sulfur, two substituted lanthanum zirconate (LZ) pyrochlores (La 2Zr 2O 7), identified in a previous study [D.J. Haynes, D.A. Berry, D. Shekhawat, J.J. Spivey, Catal. Today 136 (2008) 206], were investigated: (a) La–Rh–Zr (LRZ) and La–Sr–Rh–Zr (LSRZ). Using unsubstituted lanthanum zirconate and a conventional 0.5 wt% Rh/γ-Al 2O 3 as comparisons, these four catalysts were exposed to a feed containing 1000 ppmw dibenzothiophene (DBT) in n-tetradecane (TD). DBT rapidly deactivated both the 0.5 wt% Rh/γ-Al 2O 3 and LZ. The LRZ catalyst experienced a gradual deactivation, suggesting that Rh substitution into the pyrochlore structure, by itself, cannot completely eliminate deactivation by sulfur. However, the additional substitution of Sr stabilized yields of H 2 and CO in the presence of DBT at levels only slightly below those observed without sulfur in the feed. After sulfur was removed from the feed, each catalyst was able to recover some activity. The recovery appears to be linked to carbon formed on active sites. The 0.5 wt% Rh/γ-Al 2O 3, LZ, and LRZ all had comparable amounts of carbon formed on the surface: 0.90, 0.80 and 0.86 g carbon/g cat, respectively. Of these three catalysts, only the LRZ was able to recover a significant portion of initial activity, suggesting that the carbon formed indiscriminately on the surface, and not solely on the active sites. LSRZ was able to regain almost its initial activity once sulfur was removed from the feed, and had the least amount of carbon on the surface (0.30 g carbon/g cat). It is hypothesized that oxygen-ion mobility, which results from Sr substitution, reduces carbon formation and the deactivation by sulfur.