Abstract |
The initial stage of glycerol conversion over H-ZSM-5 zeolite has been investigated using density functional theory (DFT) calculations on an embedded cluster model consisting of 128 tetrahedrally coordinated atoms. It is found that glycerol dehydration to acrolein and acetol proceeds favourably via a stepwise mechanism. The formation of an alkoxide species upon the first dehydration requires the highest activation energy (42.5 kcal mol(-1)) and can be considered as the rate determining step of the reaction. The intrinsic activation energies for the first dehydration are virtually the same for both acrolein and acetol formation, respectively, suggesting the competitive removal of the primary and secondary OH groups. A high selectivity to acrolein at moderate temperatures can be attributed to the selective activation of the stronger adsorption mode of glycerol through the secondary OH group and the kinetically favoured subsequent consecutive steps. In addition, the less reactive nature of acrolein relative to acetol precludes it from being converted to other products upon conversion to glycerol. In accordance with typical endothermic reactions, the forward rate constant for glycerol dehydration significantly increases with increasing reaction temperature.
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Authors | Kanokwan Kongpatpanich, Tanin Nanok, Bundet Boekfa, Michael Probst, Jumras Limtrakul |
Journal | Physical chemistry chemical physics : PCCP
(Phys Chem Chem Phys)
Vol. 13
Issue 14
Pg. 6462-70
(Apr 14 2011)
ISSN: 1463-9084 [Electronic] England |
PMID | 21369602
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Aldehydes
- Alkenes
- Hydroxides
- Zeolites
- Acetone
- Acrolein
- acetol
- hydroxide ion
- propionaldehyde
- propylene
- Glycerol
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Topics |
- Acetone
(analogs & derivatives, chemistry)
- Acrolein
(chemistry)
- Aldehydes
(chemistry)
- Alkenes
(chemistry)
- Glycerol
(chemistry)
- Hydroxides
(chemistry)
- Isomerism
- Models, Molecular
- Molecular Conformation
- Quantum Theory
- Zeolites
(chemistry)
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