Microporous Mg-Si-O and Al-Si-O Materials Derived from Metal Silsesquioxanes

  • N. Maxim
  • , P.C.M.M. Magusin
  • , P.J. Kooyman
  • , J.H.M.C. Wolput, van
  • , R.A. Santen, van
  • , H.C.L. Abbenhuis

Research output: Contribution to journalArticleAcademicpeer-review

54 Citations (Scopus)

Abstract

Microporous amorphous metallosilicates designated as Mg-Si-O and Al-Si-O, with a very narrow pore size distribution around 6 .ANG. diam., typical surface areas ranging from 350 to 650 m2/g, and loadings of well-dispersed metal oxide (up to about 10 wt % metal) result from the controlled calcination of magnesium and aluminum silsesquioxane complexes [(c-C5H9)7Si7O12]2Mg4Cl2.2THF, 1, {[(c-C5H9)7Si7O12]Al}n, 2, and [(c-C5H9)7Si7O11(OSiMe3)]Al[(c-C5H9)7Si7O10(OSiMe3)(OH)], 3. Moreover, textural properties such as surface area and pore vol. can be easily adjusted by varying the calcination conditions, while the pore size distribution remains practically unchanged. XPS, EDX, solid-state MAS 29Si and 27Al NMR, and HRTEM measurements suggest that the metal is present in M-Si-O materials mainly as isolated metal ions incorporated in the amorphous silica framework and also as small cryst. metal oxide particles of a few nanometers, which are well dispersed throughout the silica. SEM was employed as well to evaluate particle size and morphol. IR spectroscopy of adsorbed acetonitrile showed that both Al-Si-O materials are strong Lewis acids. Mg-Si-O and Al-Si-O were briefly tested as catalysts in 1-butanol dehydration. Mg-Si-O gave both dehydrogenation and dehydration, while on Al-Si-O only dehydration and cracking reactions occurred. [on SciFinder (R)]
Original languageEnglish
Pages (from-to)2958-2964
JournalChemistry of Materials
Volume13
Issue number9
DOIs
Publication statusPublished - 2001

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