Reactions of ethylidene on a model chromia surface: 1,1-dichloroethane on stoichiometric α-Cr2O3 (10(1)over-bar2)

被引:1
作者
Brooks, John D. [1 ]
Chen, Tsung-Liang [2 ]
Mullins, David R. [2 ]
Cox, David F. [1 ]
机构
[1] Virginia Polytech Inst & State Univ, Dept Chem Engn, Blacksburg, VA 24061 USA
[2] Oak Ridge Natl Lab, Div Chem Sci, Oak Ridge, TN 37831 USA
关键词
Temperature programmed desorption; Chromium oxide; 1,1-dichloroethane; Halogen; Ethane dehydrogenation; Ethylidene; IRON CARBENE COMPLEXES; METHYL RADICALS; OXIDATIVE DEHYDROGENATION; ALKYLIDENE TRANSFER; CARBON-DIOXIDE; DECOMPOSITION; OXIDE; ETHYLENE; ETHANE; DEHALOGENATION;
D O I
10.1016/j.susc.2011.03.020
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
The reaction of CH3CHCl2 over the nearly-stoichiometric alpha-Cr2O3 (10 (1) over bar2) surface produces an ethylidene intermediate that yields primarily gas phase CH2=CH2 and surface chlorine adatoms: however, trace amounts of HC CH, CH3CH3, H-2 and CH3CH=CHCH3 are also observed. A rate-limiting intramolecular isomerization (2,1-hydrogen shift) in the surface ethylidene species produces gas phase CH2=CH2. The chlorine freed from the dissociation of CH3CHCl2 binds at the five-coordinate surface Cr3+ sites on the stoichiometric surface, completing the octahedral coordination sphere, and inhibits the surface chemistry by simple site blocking. No surface carbon deposition is observed from the thermal reaction of 1,1-dichloroethane under the conditions of this study, demonstrating that the ethylidene intermediate is not a primary coke forming intermediate over (10 (1) over bar2) facets of alpha-Cr2O3 under the conditions of this study. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:1170 / 1176
页数:7
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