6533b86dfe1ef96bd12ca19c
RESEARCH PRODUCT
Isolated Fe(III)-O Sites Catalyze the Hydrogenation of Acetylene in Ethylene Flows under Front-End Industrial Conditions
Francisco GonellEmilio PardoDonatella ArmentanoMarta MonJesús Ferrando-soriaAntonio Leyva-pérezMaría Tejeda-serranoAvelino CormaBethany Rosssubject
EthylenebiologyChemistryActive site02 engineering and technologyGeneral ChemistryCrystal structure010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesBiochemistryCatalysis0104 chemical sciencesCatalysischemistry.chemical_compoundColloid and Surface ChemistryQUIMICA ORGANICAAcetyleneChemical engineeringbiology.proteinCubic zirconiaMetal catalyst0210 nano-technologyEfficient catalystdescription
[EN] The search for simple, earth-abundant, cheap, and nontoxic metal catalysts able to perform industrial hydrogenations is a topic of interest, transversal to many catalytic processes. Here, we show that isolated FeIII¿O sites on solids are able to dissociate and chemoselectively transfer H2 to acetylene in an industrial process. For that, a novel, robust, and highly crystalline metal¿organic framework (MOF), embedding FeIII¿OH2 single sites within its pores, was prepared in multigram scale and used as an efficient catalyst for the hydrogenation of 1% acetylene in ethylene streams under front-end conditions. Cutting-edge X-ray crystallography allowed the resolution of the crystal structure and snapshotted the single-atom nature of the catalytic FeIII¿O site. Translation of the active site concept to even more robust and inexpensive titania and zirconia supports enabled the industrially relevant hydrogenation of acetylene with similar activity to the Pd-catalyzed process.
year | journal | country | edition | language |
---|---|---|---|---|
2018-06-26 |