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The Role of the Oxygen Vacancies in the Synthesis of 1, 3‐Butadiene from Ethanol
Author(s) -
Chagas Luciano H.,
Zonetti Priscila C.,
Matheus Caio R. V.,
Rabello Carlos R. K.,
Alves Odivaldo C.,
Appel Lucia G.
Publication year - 2019
Publication title -
chemcatchem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.497
H-Index - 106
eISSN - 1867-3899
pISSN - 1867-3880
DOI - 10.1002/cctc.201901243
Subject(s) - catalysis , dehydrogenation , acetaldehyde , chemistry , electron paramagnetic resonance , oxygen , 1,3 butadiene , inorganic chemistry , oxide , ethanol , medicinal chemistry , photochemistry , organic chemistry , physics , nuclear magnetic resonance
The t ‐ZrO 2 doped with Zn catalyst and t ‐ZrO 2 as reference were employed in the butadiene synthesis from ethanol. Both catalysts were characterized by NH 3 ‐TPD, CO 2 ‐TPD, TPSR, the MPV model reaction, ICP, BET and EPR. Adding 0.2 wt% Zn to t ‐ZrO 2 , the selectivity to butadiene increases three fold whereas the one to ethylene decreases. When ZrO 2 is doped, the number of basic sites increases and the number of acid sites decreases. The TPSR spectra indicate that the acetaldehyde generation is the rate limiting step of the butadiene synthesis. The slowest step of the acetaldehyde generation is the H abstraction by a strong basic site. The EPR spectra show the replacement of Zr 4+ by Zn 2+ in the lattice of the t ‐ZrO 2 oxide . This phenomenon forms pairs of oxygen vacancies and coordinatively unsaturated Zr 4+ ions (cus), which are strong basic sites and acid sites, respectively. Doping ZrO 2 with Zn, the ethanol dehydrogenation and the butadiene synthesis are promoted not only due to the changes in the acidity and basicity of the catalyst but mainly because of the generation of oxygen vacancies and cus pairs during the reaction. These oxygen vacancies seem to behave as strong Brønsted basic sites.

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