TY - JOUR
T1 - Dehydrogenation of bioethanol using Cu nanoparticles supported on N‐doped ordered mesoporous carbon
AU - Pulikkal Thumbayil, Rouzana
AU - Christensen, David Benjamin
AU - Mielby, Jerrik Jørgen
AU - Kegnæs, Søren
PY - 2020
Y1 - 2020
N2 - Carbon supported Cu nanoparticles have a remarkable selectivity towards the catalytic dehydrogenation of bioethanol to acetaldehyde, which is an interesting alternative to the preparation from ethylene. In this work, we prepared a series of catalysts comprised of Cu nanoparticles supported on N‐doped ordered mesoporous carbons to investigate the catalytic effect of nitrogen content. Our study shows that N‐doping has a significant effect on the dispersion of Cu nanoparticles and that the highest content of N results in the highest activity. Furthermore, we show that the combined effects of strong metal‐support interactions and nano‐confinement is an effective method to prevent thermal and steam induced sintering. In contrast, we find no evidence that N‐doping activates the substrate or change the rate‐determining step. At 260 °C, the best catalyst results in >99% selectivity and a site‐time yield of 175 mol acetaldehyde /mol Cu /h. Under these conditions, the catalysts are stable for more than 12 h using an aqueous solution of 10% ethanol as feed.
AB - Carbon supported Cu nanoparticles have a remarkable selectivity towards the catalytic dehydrogenation of bioethanol to acetaldehyde, which is an interesting alternative to the preparation from ethylene. In this work, we prepared a series of catalysts comprised of Cu nanoparticles supported on N‐doped ordered mesoporous carbons to investigate the catalytic effect of nitrogen content. Our study shows that N‐doping has a significant effect on the dispersion of Cu nanoparticles and that the highest content of N results in the highest activity. Furthermore, we show that the combined effects of strong metal‐support interactions and nano‐confinement is an effective method to prevent thermal and steam induced sintering. In contrast, we find no evidence that N‐doping activates the substrate or change the rate‐determining step. At 260 °C, the best catalyst results in >99% selectivity and a site‐time yield of 175 mol acetaldehyde /mol Cu /h. Under these conditions, the catalysts are stable for more than 12 h using an aqueous solution of 10% ethanol as feed.
U2 - 10.1002/cctc.202000883
DO - 10.1002/cctc.202000883
M3 - Journal article
SN - 1867-3880
VL - 12
SP - 5644
EP - 5655
JO - ChemCatChem
JF - ChemCatChem
IS - 22
ER -