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Catalytic effects in propene ammoxidation achieved through substitutions in the M2 phase of the Mo-V-Nb-Te-oxide system

Holmberg, Johan LU ; Hansen, Staffan LU ; Grasselli, Robert and Andersson, Arne LU (2006) In Topics in Catalysis 38(1-3). p.17-29
Abstract
M2-type phases M3TeO10 (M = Mo and V), belonging to the Mo-V-Nb-Te-oxide system, were prepared by substituting to various degrees the M-metal with W, Ti, Nb or Fe, and Te with Ce. The compositions were characterized by BET, XRD and XPS and were studied for propene ammoxidation. The variations of the unit cell parameters with substitution reveal that the orthorhombic, pseudo-hexagonal M2 structure is preserved to different degrees depending on the substituent and its amount. It is noted that partial substitution with W, Ti, Ce and Fe all increase the activity of the base composition and that Ce, and especially W, improve the selectivity to acrylonitrile at the expense of acrolein. The results of the activity measurements and the XPS... (More)
M2-type phases M3TeO10 (M = Mo and V), belonging to the Mo-V-Nb-Te-oxide system, were prepared by substituting to various degrees the M-metal with W, Ti, Nb or Fe, and Te with Ce. The compositions were characterized by BET, XRD and XPS and were studied for propene ammoxidation. The variations of the unit cell parameters with substitution reveal that the orthorhombic, pseudo-hexagonal M2 structure is preserved to different degrees depending on the substituent and its amount. It is noted that partial substitution with W, Ti, Ce and Fe all increase the activity of the base composition and that Ce, and especially W, improve the selectivity to acrylonitrile at the expense of acrolein. The results of the activity measurements and the XPS investigation indicate that the site, activating propene and ammonia on the unsubstituted M2 phase is a surface ensemble of Mo and Te. W and Ce were found to be able to mimic the role of Mo and Te, respectively; W mainly via site isolation and electronic effects, Ce via redox effects. V- and Ti-sites are shown to be inactive, having merely the role of structure adjusting elements, and serving as templates to complex the excess Te on the surface. (Less)
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author
; ; and
organization
publishing date
type
Contribution to journal
publication status
published
subject
keywords
XPS, XRD, M2-phase, substitutions, Mo-V-Nb-Te-oxide catalysts, acrylonitrile, ammoxidation, propene
in
Topics in Catalysis
volume
38
issue
1-3
pages
17 - 29
publisher
Kluwer
external identifiers
  • wos:000239592200004
  • scopus:33748805733
ISSN
1572-9028
DOI
10.1007/s11244-006-0067-9
language
English
LU publication?
yes
additional info
The information about affiliations in this record was updated in December 2015. The record was previously connected to the following departments: Polymer and Materials Chemistry (LTH) (011001041), Chemical Engineering (011001014)
id
fbe11a8e-7705-4fe9-ad2c-097e1ff91e39 (old id 398633)
date added to LUP
2016-04-01 15:29:12
date last changed
2021-10-06 01:16:32
@article{fbe11a8e-7705-4fe9-ad2c-097e1ff91e39,
  abstract     = {M2-type phases M3TeO10 (M = Mo and V), belonging to the Mo-V-Nb-Te-oxide system, were prepared by substituting to various degrees the M-metal with W, Ti, Nb or Fe, and Te with Ce. The compositions were characterized by BET, XRD and XPS and were studied for propene ammoxidation. The variations of the unit cell parameters with substitution reveal that the orthorhombic, pseudo-hexagonal M2 structure is preserved to different degrees depending on the substituent and its amount. It is noted that partial substitution with W, Ti, Ce and Fe all increase the activity of the base composition and that Ce, and especially W, improve the selectivity to acrylonitrile at the expense of acrolein. The results of the activity measurements and the XPS investigation indicate that the site, activating propene and ammonia on the unsubstituted M2 phase is a surface ensemble of Mo and Te. W and Ce were found to be able to mimic the role of Mo and Te, respectively; W mainly via site isolation and electronic effects, Ce via redox effects. V- and Ti-sites are shown to be inactive, having merely the role of structure adjusting elements, and serving as templates to complex the excess Te on the surface.},
  author       = {Holmberg, Johan and Hansen, Staffan and Grasselli, Robert and Andersson, Arne},
  issn         = {1572-9028},
  language     = {eng},
  number       = {1-3},
  pages        = {17--29},
  publisher    = {Kluwer},
  series       = {Topics in Catalysis},
  title        = {Catalytic effects in propene ammoxidation achieved through substitutions in the M2 phase of the Mo-V-Nb-Te-oxide system},
  url          = {http://dx.doi.org/10.1007/s11244-006-0067-9},
  doi          = {10.1007/s11244-006-0067-9},
  volume       = {38},
  year         = {2006},
}