SYNTHESIS AND CHARACTERIZATION OF OCTAHEDRAL MOLECULAR-SIEVES (OMS-2)HAVING THE HOLLANDITE STRUCTURE

Citation
Rn. Deguzman et al., SYNTHESIS AND CHARACTERIZATION OF OCTAHEDRAL MOLECULAR-SIEVES (OMS-2)HAVING THE HOLLANDITE STRUCTURE, Chemistry of materials, 6(6), 1994, pp. 815-821
Citations number
29
Categorie Soggetti
Chemistry Physical","Material Science
Journal title
ISSN journal
08974756
Volume
6
Issue
6
Year of publication
1994
Pages
815 - 821
Database
ISI
SICI code
0897-4756(1994)6:6<815:SACOOM>2.0.ZU;2-7
Abstract
Hollandite and cryptomelane materials have been prepared using two dif ferent methods. Octahedral molecular sieve (OMS) having the 2 x 2 holl andite structure with a one-dimensional pore diameter of 4.6 angstrom. Synthetic cryptomelane or OMS-2 can be formed by refluxing or autocla ving an acidic solution of KMnO4 and Mn2+. Temperature, pH, and counte rcation are important synthetic parameters. The hollandite formed show s thermal stability up to 600-degrees-C. OMS-2 formed by oxidation of Mn2+ under basic conditions and calcined at higher temperature (200-80 0-degrees-C) is thermally stable up to 800-degrees-C. X-ray powder dif fraction and electron diffraction patterns have been simulated that sh ow good agreement with experimental data supporting a tetragonal cryst al system in the I4/m space group. Hollandites were also prepared in t he presence of other transition-metal ions such as Cu2+ and Fe3+. The Cu2+ and Fe3+-doped OMS-2 materials were prepared by refluxing a solut ion of MnO4- and Mn2+ with Cu2+ or Fe3+. Electron paramagnetic resonan ce (EPR) data show that OMS-2 materials synthesized in the presence of Cu2+ and Fe3+ contain nonexchangeable Mn2+. EPR data for Cu-OMS-2 sho wed a characteristic six-line pattern with a g value of 2.0 and an A v alue of 85 G indicative of octahedral Mn2+ coordination. The Mn2+ EPR peaks in Fe-OMS-2 showed similar g and A values. EPR spectra, ion-exch ange data, X-ray diffraction patterns, and theoretical simulations of diffraction data suggest that Cu2+ and Fe3+ are located in the tunnels of OMS-2.