Deoxydehydration of Biomass-Derived Polyols with a Reusable Unsupported Rhenium Nanoparticles Catalyst

Authors
Jang, Jun HeeSohn, HyuntaeCamacho-Bunquin, JeffreyYang, DaliPark, Chan Y.Delferro, MassimilianoAbu-Omar, Mahdi M.
Issue Date
2019-07
Publisher
American Chemical Society
Citation
ACS Sustainable Chemistry & Engineering, v.7, no.13, pp.11438 - 11447
Abstract
Oxorhenium catalysts effectively transform biomass derived polyols into corresponding alkenes via deoxydehydration (DODH) with a secondary alcohol as a hydrogen donor. This study describes the preparation of unsupported rhenium oxide nano particles (ReOx NPs), their use as DODH heterogeneous catalyst, and changes in the speciation and structure of Re during catalysis leading to a possible mechanism for DODH by a heterogeneous catalyst. The unsupported nanoparticles catalyze various polyols transformation to produce alkenes with high efficiency and recyclability. X-ray spectroscopy analysis shows that the structure of as-prepared ReOx NPs is similar to perrhenate with oxidation state between Re(VI) and Re(VII). Under reaction conditions and postcatalysis, the ReOx NPs are reduced by approximately two oxidation units. Kinetic isotope effect demonstrates that dissociation of a C-H bond during reduction of ReOx NPs by 3-octanol is part of the rate-determining step. Based on all experimental observations, the mechanism of DODH catalysis with unsupported ReOx NPs involving a Re(VII)/Re(V) redox pair is proposed.
Keywords
SULFITE-DRIVEN; ALLYL ALCOHOL; DIOLS; ALKENES; MECHANISM; DEOXYGENATION; CONVERSION; CHEMICALS; GLYCEROL; HYDROGEN; Deoxydehydration; Rhenium; Unsupported nanoparticle; Heterogeneous catalysis; Mechanism; Glycerol
ISSN
2168-0485
URI
https://pubs.kist.re.kr/handle/201004/119798
DOI
10.1021/acssuschemeng.9b01253
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KIST Article > 2019
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