Journal
MATERIALS RESEARCH EXPRESS
Volume 6, Issue 7, Pages -Publisher
IOP PUBLISHING LTD
DOI: 10.1088/2053-1591/ab12be
Keywords
nanomaterial; TUD-1; TUD-C; mesostructure; epoxidation; solid acid catalysis; titania
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Funding
- Ministry of Higher Education, Malaysia (MOHE)
- Universiti Teknologi Malaysia (UTM) [Q.J130000.2526.13H52, Q.J130000.2526.16H17, Q.J130000.3554.07G57]
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A direct comparison between nanostructured Technische Universiteit Delft-1 (TUD-1) and Technische Universiteit Delft-Crystalline (TUD-C) as catalyst supports for molybdenum doped titania catalysts was carried out. The characterizations results showed that TUD-1 is a mesoporous amorphous silicate material with high surface area and porosity. Meanwhile, TUD-C is an ordered mesoporous crystalline aluminosilicate matters featured high acidity. In fact, TUD-C was obtained from the modification of TUD-1 with the addition of aluminium isopropoxide as the zeolite precursor. The catalytic testing demonstrated TUD-1 supported 1 mol% molybdena doped titania was inactive for epoxidation of 1,2-epoxyoctane and showed moderate activity (18%-21% conversion yield) and selectivity (approximately 70%) in epoxidation reaction of 1,2-epoxycyclohexane (0.51 mmol) and styrene oxide (1.25 mmol). Meanwhile, TUD-C supported 1 mol% molybdena doped titania achieved remarkably higher conversion yield for 1,2-epoxyoctane (2.7 mmol), 1,2-epoxycyclohexane (4.8 mmol) and styrene oxide (6.2 mmol) respectively with 100% selectivity towards all 3 analytes under ambient condition with constant stirring. The results strongly indicated that high Bronsted and Lewis acidic sites existed within the TUD-C framework is the key factor for the exceptional oxidative capabilities for molybdena-titania catalysts.
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