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B-MWW 沸石:反对单中心催化的案例

B-MWW Zeolite: The Case Against Single-Site Catalysis.

作者信息

Altvater Natalie R, Dorn Rick W, Cendejas Melissa C, McDermott William P, Thomas Brijith, Rossini Aaron J, Hermans Ive

机构信息

Department of Chemical and Biological Engineering, University of Madison - Wisconsin, 1415 Engineering Drive, Madison, WI, 53706, USA.

Department of Chemistry, Iowa State University, 2438 Pammel Dr., Ames, IA, 50011, USA.

出版信息

Angew Chem Int Ed Engl. 2020 Apr 16;59(16):6546-6550. doi: 10.1002/anie.201914696. Epub 2020 Feb 28.

Abstract

Boron-containing materials have recently been identified as highly selective catalysts for the oxidative dehydrogenation (ODH) of alkanes to olefins. It has previously been demonstrated by several spectroscopic characterization techniques that the surface of these boron-containing ODH catalysts oxidize and hydrolyze under reaction conditions, forming an amorphous B (OH) O (x=0-6) layer. Yet, the precise nature of the active site(s) remains elusive. In this Communication, we provide a detailed characterization of zeolite MCM-22 isomorphously substituted with boron (B-MWW). Using B solid-state NMR spectroscopy, we show that the majority of boron species in B-MWW exist as isolated BO units, fully incorporated into the zeolite framework. However, this material shows no catalytic activity for ODH of propane to propene. The catalytic inactivity of B-MWW for ODH of propane falsifies the hypothesis that site-isolated BO units are the active site in boron-based catalysts. This observation is at odds with other traditionally studied catalysts like vanadium-based catalysts and provides an important piece of the mechanistic puzzle.

摘要

含硼材料最近被确定为用于烷烃氧化脱氢(ODH)制烯烃的高选择性催化剂。此前已有多种光谱表征技术证明,这些含硼ODH催化剂的表面在反应条件下会发生氧化和水解,形成非晶态的B(OH)O(x = 0 - 6)层。然而,活性位点的确切性质仍然难以捉摸。在本通讯中,我们对同晶置换硼的沸石MCM - 22(B - MWW)进行了详细表征。使用硼固态核磁共振光谱,我们表明B - MWW中的大多数硼物种以孤立的BO单元形式存在,完全融入沸石骨架中。然而,这种材料对丙烷氧化脱氢制丙烯没有催化活性。B - MWW对丙烷氧化脱氢的催化无活性证明了位点孤立的BO单元是硼基催化剂中的活性位点这一假设是错误的。这一观察结果与钒基催化剂等其他传统研究的催化剂不同,并为机理难题提供了重要的一环。

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