TY - JOUR
T1 - Insights into the deactivation mechanism of supported tungsten hydride on alumina (W-H/Al2O3) catalyst for the direct conversion of ethylene to propylene
AU - Mazoyer, Etienne
AU - Szeto, Kaï Chung
AU - Merle, Nicolas
AU - Thivolle-Cazat, Jean
AU - Boyron, Olivier
AU - Basset, Jean-Marie
AU - Nicholas, Christopher P.
AU - Taoufik, Mostafa
N1 - KAUST Repository Item: Exported on 2020-10-01
PY - 2014/4
Y1 - 2014/4
N2 - Tungsten hydride supported on alumina prepared by the surface organometallic chemistry method is an active precursor for the direct conversion of ethylene to propylene at low temperature and pressure. An extensive contact time study revealed that the dimerization of ethylene to 1-butene is the primary and also the rate limiting step. The catalytic cycle further involves isomerization of 1-butene to 2-butene, followed by cross-metathesis of ethylene and 2-butene to yield propylene with high selectivity. The deactivation mechanism of this reaction has been investigated. The used catalyst was extensively examined by DRIFTS, solid-state NMR, EPR, UV-Vis, TGA and DSC techniques. It was found that a large amount of carbonaceous species, which were due to side reaction like olefin polymerization took place with time on stream, significantly hindering the dimerization of ethylene to 1-butene and therefore the production of propylene. Crown Copyright © 2014 Published by Elsevier B.V. All rights reserved.
AB - Tungsten hydride supported on alumina prepared by the surface organometallic chemistry method is an active precursor for the direct conversion of ethylene to propylene at low temperature and pressure. An extensive contact time study revealed that the dimerization of ethylene to 1-butene is the primary and also the rate limiting step. The catalytic cycle further involves isomerization of 1-butene to 2-butene, followed by cross-metathesis of ethylene and 2-butene to yield propylene with high selectivity. The deactivation mechanism of this reaction has been investigated. The used catalyst was extensively examined by DRIFTS, solid-state NMR, EPR, UV-Vis, TGA and DSC techniques. It was found that a large amount of carbonaceous species, which were due to side reaction like olefin polymerization took place with time on stream, significantly hindering the dimerization of ethylene to 1-butene and therefore the production of propylene. Crown Copyright © 2014 Published by Elsevier B.V. All rights reserved.
UR - http://hdl.handle.net/10754/563472
UR - https://linkinghub.elsevier.com/retrieve/pii/S1381116914000260
UR - http://www.scopus.com/inward/record.url?scp=84894619997&partnerID=8YFLogxK
U2 - 10.1016/j.molcata.2014.01.025
DO - 10.1016/j.molcata.2014.01.025
M3 - Article
SN - 1381-1169
VL - 385
SP - 125
EP - 132
JO - Journal of Molecular Catalysis A: Chemical
JF - Journal of Molecular Catalysis A: Chemical
ER -