Edge‐hydroxylated Boron Nitride for Oxidative Dehydrogenation of Propane to Propylene
Oxidative dehydrogenation of propane to olefins is a promising alternative route to industrialized direct dehydrogenation, but encounters the difficulty in selectivity control for olefins because of the overoxidation reactions that produce a substantial amount of undesired CO2. Here we report edge‐h...
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Published in | ChemCatChem Vol. 9; no. 10; pp. 1788 - 1793 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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Abstract | Oxidative dehydrogenation of propane to olefins is a promising alternative route to industrialized direct dehydrogenation, but encounters the difficulty in selectivity control for olefins because of the overoxidation reactions that produce a substantial amount of undesired CO2. Here we report edge‐hydroxylated boron nitride, a metal‐free catalyst, that efficiently catalyzed dehydrogenation of propane to propylene with superior selectivity (80.2 %) but with only negligible CO2 formation (0.5 %) at a given propane conversion of 20.6 %. Remarkable stability was evidenced by the operation of a 300 h test with steady conversion and product selectivity. The active BNO. site, generated dynamically through hydrogen ion of B−OH groups by molecular oxygen, triggered propane dehydrogenation by selectively breaking the C−H bond but simultaneously shut off the pathway of propylene overoxidation towards CO2.
Olefin generation without a metal: Edge‐hydroxylated boron nitride shows superior selectivity for the oxidative dehydrogenation of propane to propylene with only negligible CO2 formation. The dynamically generated active BNO. site triggers propane dehydrogenation by selectively breaking the C−H bond by concomitantly avoiding propylene oxidation to CO2. |
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AbstractList | Oxidative dehydrogenation of propane to olefins is a promising alternative route to industrialized direct dehydrogenation, but encounters the difficulty in selectivity control for olefins because of the overoxidation reactions that produce a substantial amount of undesired CO
2
. Here we report edge‐hydroxylated boron nitride, a metal‐free catalyst, that efficiently catalyzed dehydrogenation of propane to propylene with superior selectivity (80.2 %) but with only negligible CO
2
formation (0.5 %) at a given propane conversion of 20.6 %. Remarkable stability was evidenced by the operation of a 300 h test with steady conversion and product selectivity. The active BNO
.
site, generated dynamically through hydrogen abstraction of B−OH groups by molecular oxygen, triggered propane dehydrogenation by selectively breaking the C−H bond but simultaneously shut off the pathway of propylene overoxidation towards CO
2
. Oxidative dehydrogenation of propane to olefins is a promising alternative route to industrialized direct dehydrogenation, but encounters the difficulty in selectivity control for olefins because of the overoxidation reactions that produce a substantial amount of undesired CO2. Here we report edge-hydroxylated boron nitride, a metal-free catalyst, that efficiently catalyzed dehydrogenation of propane to propylene with superior selectivity (80.2%) but with only negligible CO2 formation (0.5%) at a given propane conversion of 20.6%. Remarkable stability was evidenced by the operation of a 300h test with steady conversion and product selectivity. The active BNO. site, generated dynamically through hydrogen abstraction of B-OH groups by molecular oxygen, triggered propane dehydrogenation by selectively breaking the C-H bond but simultaneously shut off the pathway of propylene overoxidation towards CO2. Oxidative dehydrogenation of propane to olefins is a promising alternative route to industrialized direct dehydrogenation, but encounters the difficulty in selectivity control for olefins because of the overoxidation reactions that produce a substantial amount of undesired CO2. Here we report edge‐hydroxylated boron nitride, a metal‐free catalyst, that efficiently catalyzed dehydrogenation of propane to propylene with superior selectivity (80.2 %) but with only negligible CO2 formation (0.5 %) at a given propane conversion of 20.6 %. Remarkable stability was evidenced by the operation of a 300 h test with steady conversion and product selectivity. The active BNO. site, generated dynamically through hydrogen ion of B−OH groups by molecular oxygen, triggered propane dehydrogenation by selectively breaking the C−H bond but simultaneously shut off the pathway of propylene overoxidation towards CO2. Olefin generation without a metal: Edge‐hydroxylated boron nitride shows superior selectivity for the oxidative dehydrogenation of propane to propylene with only negligible CO2 formation. The dynamically generated active BNO. site triggers propane dehydrogenation by selectively breaking the C−H bond by concomitantly avoiding propylene oxidation to CO2. |
Author | Wang, Dongqi Shi, Lei Lu, An‐Hui Song, Wei Shao, Dan Zhang, Wei‐Ping |
Author_xml | – sequence: 1 givenname: Lei surname: Shi fullname: Shi, Lei organization: Dalian University of Technology – sequence: 2 givenname: Dongqi surname: Wang fullname: Wang, Dongqi organization: Chinese Academy of Sciences – sequence: 3 givenname: Wei surname: Song fullname: Song, Wei organization: Dalian University of Technology – sequence: 4 givenname: Dan surname: Shao fullname: Shao, Dan organization: Dalian University of Technology – sequence: 5 givenname: Wei‐Ping surname: Zhang fullname: Zhang, Wei‐Ping organization: Dalian University of Technology – sequence: 6 givenname: An‐Hui surname: Lu fullname: Lu, An‐Hui email: anhuilu@dlut.edu.cn organization: Dalian University of Technology |
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Snippet | Oxidative dehydrogenation of propane to olefins is a promising alternative route to industrialized direct dehydrogenation, but encounters the difficulty in... |
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SubjectTerms | Alkenes boron Boron nitride Carbon dioxide Conversion Dehydrogenation hydrocarbons Hydrogen bonds hydroxylation nitrides Oxygen Propane Propylene Selectivity |
Title | Edge‐hydroxylated Boron Nitride for Oxidative Dehydrogenation of Propane to Propylene |
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