Effect of manganese substitution on the physicochemical properties and catalytic toluene oxidation activities of Mg-Al layered double hydroxides

Citation
S. Velu et al., Effect of manganese substitution on the physicochemical properties and catalytic toluene oxidation activities of Mg-Al layered double hydroxides, MICROP M M, 33(1-3), 1999, pp. 61-75
Citations number
46
Categorie Soggetti
Apllied Physucs/Condensed Matter/Materiales Science
Journal title
MICROPOROUS AND MESOPOROUS MATERIALS
ISSN journal
13871811 → ACNP
Volume
33
Issue
1-3
Year of publication
1999
Pages
61 - 75
Database
ISI
SICI code
1387-1811(199912)33:1-3<61:EOMSOT>2.0.ZU;2-6
Abstract
A series of Mg-Mn-Al ternary hydrotalcite-like layered double hydroxides (L DHs) with (Mg+Mn)/Al atomic ratios of similar to 3 and Mg:Mn atomic ratios ranging from 3:0 to 0:3 were synthesized by a co-precipitation method. The incorporation of Mn in the MgAl-LDH was investigated by employing various t echniques, such as powder X-ray diffraction, Fourier transform infrared spe ctroscopy, electron paramagetic resonance (EPR) spectroscopy, UV-visible di ffuse-reflectance spectroscopy (UV-Vis DRS) and thermogravimetry. A single phase corresponding to LDH was obtained up to the composition Mg:Mn:Al=2.2: 0.8:1. A further increase in the Mn content resulted in the formation of a mixture of LDH, Mn(OH), and MnCO3 phases. Partial oxidation of Mn2+ to Mn3 took place during synthesis, as evidenced by UV-Vis DRS. According to the EPR and UV-Vis DRS results, the Mn2+/Mn3+ ions were present in a (distorted ) octahedral environment. Calcination at 723 K resulted in the formation of a poorly crystalline MgO-like solid solution. Mn retained its +2 oxidation state (EPR active) even upon calcination at very high temperature (1473 K) in air. At a higher Mn content, in addition to the MgO-like phase, spinel phases such as Mn3O4 and MnAl2O4 were also obtained at 723 K. The catalytic activity of the as-synthesized samples was tested in the liquid-phase oxid ation of toluene using tert-butyl hydroperoxide as the oxidant. Benzaldehyd e and benzoic acid were the major products with minor amounts of benzyl alc ohol. The compound without an LDH phase was found to be less active for the oxidation of toluene under similar reaction conditions. Solvents were foun d to have a profound influence on the catalytic activity and the product se lectivity. (C) 1999 Elsevier Science B.V. All rights reserved.