Yee, Khai Ooi and Hussin, Faisal and Yuliati, Leny and Siew, Ling Lee (2019) Comparison study on Molybdena-Titania supported on TUD-1 and TUD-C synthesized via sol-gel templating method: properties and catalytic performance in olefins epoxidation. Materials Research Express, 6 (7). 074001-074001. ISSN 2053-1591
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Official URL: http://dx.doi.org/10.1088/2053-1591/ab12be
Abstract
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.
Item Type: | Article |
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Uncontrolled Keywords: | mesostructure, nanomaterial, solid acid catalysis |
Subjects: | Q Science > QD Chemistry |
Divisions: | Science |
ID Code: | 87697 |
Deposited By: | Yanti Mohd Shah |
Deposited On: | 30 Nov 2020 13:08 |
Last Modified: | 30 Nov 2020 13:08 |
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