Publications by authors named "William V Knowles"

A time-resolved in situ micro-spectroscopic approach has been used to investigate the Brønsted acidic properties of fluid-catalytic-cracking (FCC) catalysts at the single particle level by applying the acid-catalysed styrene oligomerisation probe reaction. The reactivity of individual FCC components (zeolite, clay, alumina and silica) was monitored by UV/Vis micro-spectroscopy and showed that only clay and zeolites (Y and ZSM-5) contain Brønsted acid sites that are strong enough to catalyse the conversion of 4-fluorostyrene into carbocationic species. By applying the same approach to complete FCC catalyst particles, it has been found that the fingerprint of the zeolitic UV/Vis spectra is clearly recognisable.

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Fluid catalytic cracking (FCC) is the major conversion process used in oil refineries to produce valuable hydrocarbons from crude oil fractions. Because the demand for oil-based products is ever increasing, research has been ongoing to improve the performance of FCC catalyst particles, which are complex mixtures of zeolite and binder materials. Unfortunately, there is limited insight into the distribution and activity of individual zeolitic domains at different life stages.

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Tungstated zirconia is a robust solid acid catalyst for light alkane (C(4)-C(8)) isomerization. Several structural models for catalytically active sites have been proposed, but the topic remains controversial, partly because of the absence of direct structural imaging information on the various supported WO(x) species. High-angle annular dark-field imaging of WO(3)/ZrO(2) catalysts in an aberration-corrected analytical electron microscope allows, for the first time, direct imaging of the various species present.

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Article Synopsis
  • A variety of TiO(2)/SiO(2) catalysts were developed to incorporate VO(x) and WO(x) active sites for catalytic reactions.
  • Characterization techniques like TEM, Raman, and UV-vis spectroscopy helped confirm the properties of these catalysts, revealing that VO(x) sites are redox-active while WO(x) sites have acidic properties.
  • The study found that decreasing the size of titania domains (less than 10 nm) enhances acidic activity but reduces redox activity due to their opposing electronic demands, marking a novel approach in modifying catalyst properties using oxide nanoligands.
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