Identifying Boron Active Sites for the Oxidative Dehydrogenation of Propane

被引:34
作者
Yan, Huan [1 ]
Alayoglu, Selim [2 ]
Wu, Weiqiang [2 ]
Zhang, Yongbo [3 ]
Weitz, Eric [1 ]
Stair, Peter C. [1 ]
Notestein, Justin M. [4 ]
机构
[1] Northwestern Univ, Dept Chem, Evanston, IL 60208 USA
[2] Northwestern Univ, Ctr Catalysis & Surface Sci, Evanston, IL 60208 USA
[3] Northwestern Univ, Integrated Mol Struct Educ & Res Ctr, Evanston, IL 60208 USA
[4] Northwestern Univ, Dept Chem & Biol Engn, Evanston, IL 60208 USA
基金
美国国家科学基金会;
关键词
ODHP; NMR; selective oxidation; silica; propylene; precursor; RAMAN-SPECTROSCOPY; OXIDE CATALYSTS; NMR; ETHANE; ZEOLITE; GLASSES;
D O I
10.1021/acscatal.1c02168
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Oxidative dehydrogenation of propane (ODHP) to propylene could have a significant impact on the production of this critical chemical intermediate, if appropriate catalysts can be discovered. Recently, heterogeneous catalysts based on boron (oxides and nitrides) have been demonstrated to be promising for ODHP, but their active sites have not been conclusively identified. Here, we report that the deposition of differently sized boronic acids into the micropores of silica supports results in different distributions of surface borate species after calcination. These materials, in turn, display a wide range of rates in ODHP but similar selectivity, suggesting that they differ only in the numbers of active sites. Features identified by in situ Raman, IR, and magic-angle-spinning B-11 solid-state NMR spectroscopies are compared to catalyst activity. This correlation identifies the S2 borate species, a hydroxylated nonring boron, as the likely active site and provides a target for directed syntheses of future catalysts.
引用
收藏
页码:9370 / 9376
页数:7
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