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Title: Structural characteristics and catalytic properties of highly dispersed ZrO{sub 2}/SiO{sub 2} and V{sub 2}O{sub 5}/ZrO{sub 2}/SiO{sub 2} catalysts

Journal Article · · Langmuir
DOI:https://doi.org/10.1021/la981254p· OSTI ID:350243
;  [1];  [2]
  1. Lehigh Univ., Bethlehem, PA (United States)
  2. CSIC, Madrid (Spain). Inst. de Catalisis y Petroleoquimica

Highly dispersed ZrO{sub 2}/SiO{sub 2} and V{sub 2}O{sub 5}/ZrO{sub 2}/SiO{sub 2} catalysts were successfully synthesized by the incipient wetness impregnation method. The surface structures of these catalysts in hydrated and dehydrated states were characterized by in situ Raman and UV-vis-near-infrared diffuse reflectance spectroscopies. Temperature-programmed reduction and methanol oxidation were employed as chemical probe reactions to examine the reducibility and reactivity/selectivity properties of these catalysts. These characterization techniques demonstrate that both zirconium oxide and vanadium oxide species are highly dispersed as two-dimensional metal oxide overlayers on the silica support. The spectroscopic results revealed that the surface vanadium oxide species on the highly dispersed ZrO{sub 2}/SiO{sub 2} supports are predominantly isolated VO{sub 4} units [O{double_bond}V(O-Support){sub 3}] in the dehydrated state and become polymerized vanadium oxide species upon hydration. The surface vanadium oxide species preferentially interact with the zirconium oxide species on the silica surface. The substitution of Si{sup IV}-O{sup {minus}} by Zr{sup IV}-O{sup {minus}} ligands significantly affects the chemical properties of the isolated VO{sub 4} units: the reducibility of the surface vanadium oxide species increases, and the methanol oxidation turnover frequency (TOF) increases by 1--2 orders of magnitude relative to V{sub 2}O{sub 5}/SiO{sub 2}. The present study demonstrates that the support effect, variation in the reactivity of supported metal oxide catalysts due to different oxide supports, essentially originates from the difference in oxygenated ligands around the active metal cations.

Sponsoring Organization:
National Science Foundation, Washington, DC (United States); USDOE, Washington, DC (United States)
DOE Contract Number:
FG02-93ER14350
OSTI ID:
350243
Journal Information:
Langmuir, Vol. 15, Issue 9; Other Information: PBD: 27 Apr 1999
Country of Publication:
United States
Language:
English

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