Synergy effect between Zr and Cr active sites in binary CrZrOx or supported CrOx/LaZrOx: Consequences for catalyst activity, selectivity and durability in non-oxidative propane dehydrogenation

被引:80
作者
Otroshchenko, Tatiana P. [1 ]
Rodemerck, Uwe [1 ]
Linke, David [1 ]
Kondratenko, Evgenii V. [1 ]
机构
[1] Univ Rostock, Leibniz Inst Katalyse eV, Albert Einstein Str 29a, D-18059 Rostock, Germany
关键词
Dehydrogenation; Propane; Propene; Zirconia; Chromia; Coordinatively unsaturated cations; Mechanism; Reaction pathways; CHROMIA-ZIRCONIA CATALYSTS; ISOBUTANE DEHYDROGENATION; ALUMINA CATALYSTS; COKE FORMATION; N-BUTANE; PERFORMANCE; LANTHANA; OXIDES;
D O I
10.1016/j.jcat.2017.10.012
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
Bulk CrZrOx, supported CrOx/LaZrOx, and CrOx/Al2O3 catalysts were prepared with Cr surface site density varying between 0.04 and 2.3 nm(-2). They were characterized by BET, XRD, temperature-programmed reduction with H-2, and NH3 temperature-programmed desorption. Their activity, selectivity, and durability in non-oxidative propane dehydrogenation (PDH) were determined under industrially relevant conditions. The catalysts on the basis of ZrO2 outperform their Al2O3-based counterparts in terms of PDH activity. This was explained by the presence of two catalytically active sites, i.e. CrOx and coordinatively unsaturated Zr4+ (Zrcus) sites. The former species promote formation of Zrc, under reaction conditions or upon reductive catalyst treatment. Practical relevance of CrZrOx and CrOxiLaZrO(x) catalysts was checked in a series of 10 PDH/regeneration cycles performed at 550 degrees C. The catalysts possessing up to 40 times lower chromium content performed superior to an analogue of commercial K-CrOx/Al2O3 with respect to space time yield of propene and the amount of propene formed within one PDH cycle. In terms of durability, bulk promoting of ZrO2 with Cr was found to be advantageous over simple deposition of CrOx on the surface of LaZrOx. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:197 / 205
页数:9
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