Elucidation of Anchoring and Restructuring Steps during Synthesis of Silica-Supported Vanadium Oxide Catalysts
Author(s) -
Alyssa M. Love,
Carlos A. Carrero,
Alessandro Chieregato,
Joseph T. Grant,
Sabrina Conrad,
René Verel,
Ive Hermans
Publication year - 2016
Publication title -
chemistry of materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.741
H-Index - 375
eISSN - 1520-5002
pISSN - 0897-4756
DOI - 10.1021/acs.chemmater.6b02118
Subject(s) - silanol , vanadium , vanadium oxide , calcination , thermogravimetric analysis , catalysis , chemistry , diffuse reflectance infrared fourier transform , inorganic chemistry , x ray absorption spectroscopy , infrared spectroscopy , materials science , absorption spectroscopy , organic chemistry , photocatalysis , physics , quantum mechanics
We investigate the chemical reactions involved during the synthesis of supported vanadium oxide catalysts using chemical grafting of vanadium oxytriisopropoxide (VO(OiPr)3) to thermally pretreated silica under solvent-free conditions. VO(OiPr)3 is found to react with both site-isolated silanol (Si−OH) groups and strained siloxane (≡Si−O−Si≡) bridges at the silica surface. Solid-state 51V and 13C MAS NMR confirms the formation of two slightly different vanadium species associated with the two anchoring mechanisms. In situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS), in situ Raman spectroscopy, and thermogravimetric analysis-differential scanning calorimetry-mass spectrometry (TGA-DSC-MS) were used to study the subsequent calcination, revealing the formation of a transient V—OH intermediate upon the release of propene, followed by the formation of isolated VO4 surface species upon elimination of water. X-ray absorption spectroscopy (XAS) and 51V MAS NMR of the calcined material conf...
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