Loading…
A high performance multi-walled carbon nanotube-supported palladium catalyst in selective hydrogenation of acetylene-ethylene mixtures
[Display omitted] ► 0.5% pd/MWCNT displayed 93% ethylene yield in selective hydrogenation of acetylene. ► By temperature rising, ethylene selectivity and acetylene conversion were enhanced. ► At elevated temperatures, hydrogenation in tail-end process occurs in a single reactor. ► Suppressing of oli...
Saved in:
Published in: | Applied catalysis. A, General General, 2011-05, Vol.399 (1), p.184-190 |
---|---|
Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | [Display omitted]
► 0.5% pd/MWCNT displayed 93% ethylene yield in selective hydrogenation of acetylene. ► By temperature rising, ethylene selectivity and acetylene conversion were enhanced. ► At elevated temperatures, hydrogenation in tail-end process occurs in a single reactor. ► Suppressing of oligomers and displaying high stability are features of this catalyst. ► Hydrogen transfer mechanism plays an essential role over Pd/MWCNT catalyst.
In this research, a palladium nanocatalyst was synthesised over a multi-walled carbon nanotube (MWCNT) support and then applied for selective hydrogenation of acetylene in an ethylene-richflow stream. This material displayed a very promising selectivity toward ethylene production with increasing temperature, and also suppressed oligomer formation during acetylene hydrogenation. New operating conditions for selective hydrogenation of acetylene in an ethylene-richflow were introduced. This nanocatalyst gave a considerably higher yield, as high as 93%, than that previously obtained for ethylene production. It was postulated that the governing mechanism for acetylene hydrogenation over 0.5
wt.% Pd/MWCNT was hydrogen transfer. |
---|---|
ISSN: | 0926-860X 1873-3875 |
DOI: | 10.1016/j.apcata.2011.03.055 |