A. Burrows et al., STRUCTURE FUNCTION RELATIONSHIPS IN MGO-DOPED ND2O3 CATALYSTS FOR THEMETHANE COUPLING REACTION/, Journal of catalysis, 173(2), 1998, pp. 383-398
The work presented in this paper extends a previous study of catalysts
based on mixtures of MgO and Nd2O3 used in the oxidation coupling of
methane (OCM) reaction. MgO-doped neodymia catalysts have been prepare
d by two different methods with various MgO loadings and their methane
coupling performance compared with that of pure Nd2O3 Quite dramatic
differences in catalytic performance have been observed between cataly
sts prepared by coprecipitation (Series A) and impregnation (Series B)
. Particularly striking is the highly beneficial effect on activity an
d Cz selectivity that the addition of 10 at.% MgO has on the Series B
material. In both cases catalytic performance was related to the struc
tural form of the material, Structural details for these catalysts hav
e been obtained from high-resolution electron microscopy observations
and powder X-ray diffraction. The results show that the microstructure
of pure Nd2O3 is significantly different depending on the preparation
route: Series A material contains Nd2O3 in various states ranging fro
m areas having a high degree of crystallinity to extensive regions of
semicrystalline/disordered material, whereas Series B Nd2O3 was almost
exclusively in the hexagonal form, In general, MgO-doped neodymia cat
alyst materials have also been found to contain a complex mixture of N
d2O3 phases which for Series B materials became apparent after adding
up to 3 at.% MgO, With a scanning transmission electron microscope, it
has been determined that Mg2+ dissolution into the neodymia (up to 2.
5 at.%) almost certainly takes place, This result in particular may ex
plain the synergistic effect observed for OCM catalysts of this type,
(C) 1998 Academic Press.