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Dehydrocyclization of C.sub.6 Hydrocarbon With and Without Oxygen Containing Substituent Over Pt
by
Gnanamani, Muthu Kumaran
, Keogh, Robert A
, Shafer, Wilson D
, Davis, Burtron H
in
Benzene
2016
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Dehydrocyclization of C.sub.6 Hydrocarbon With and Without Oxygen Containing Substituent Over Pt
by
Gnanamani, Muthu Kumaran
, Keogh, Robert A
, Shafer, Wilson D
, Davis, Burtron H
in
Benzene
2016
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Dehydrocyclization of C.sub.6 Hydrocarbon With and Without Oxygen Containing Substituent Over Pt
Journal Article
Dehydrocyclization of C.sub.6 Hydrocarbon With and Without Oxygen Containing Substituent Over Pt
2016
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Overview
The presence of hydroxyl or keto functional group affects both activity and selectivity for dehydrocyclization of C.sub.6 hydrocarbon over Pt/(Na)-Al.sub.2O.sub.3 catalyst. Under similar reaction conditions, n-hexane produces benzene as the primary product (>40 %), whereas dehydration is a major reaction pathway for 2-hexanol and yields mainly hexenes (>70 %). However, 2-hexanone was found to be involved in a variety of reactions over Pt/(Na)-Al.sub.2O.sub.3 catalyst and produces lower hydrocarbons (C.sub.2-C.sub.5), 5-dodecanone, 2- and 5-nonanones, and 2-acetyl-3-propyl-2-cyclohexen-1-one. The presence of hydroxyl (-OH) or keto group (=C=O) at the C-2 position alters the interaction of C.sub.6 hydrocarbon with the catalyst surface which eventually controls the overall product selectivity.
Publisher
Springer
Subject
MBRLCatalogueRelatedBooks
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