AL-27 MAGIC-ANGLE-SPINNING NUCLEAR-MAGNETIC-RESONANCE SPECTROSCOPIC STUDY OF THE CONVERSION OF BASIC DICARBOXYLATE ALUMINUM(III) COMPLEXES TO ALUMINA AND ALUMINUM NITRIDE

Citation
Ws. Jung et al., AL-27 MAGIC-ANGLE-SPINNING NUCLEAR-MAGNETIC-RESONANCE SPECTROSCOPIC STUDY OF THE CONVERSION OF BASIC DICARBOXYLATE ALUMINUM(III) COMPLEXES TO ALUMINA AND ALUMINUM NITRIDE, Journal of materials chemistry (Print), 8(8), 1998, pp. 1869-1873
Citations number
25
Categorie Soggetti
Chemistry Physical","Material Science
ISSN journal
09599428
Volume
8
Issue
8
Year of publication
1998
Pages
1869 - 1873
Database
ISI
SICI code
0959-9428(1998)8:8<1869:AMNSS>2.0.ZU;2-1
Abstract
The process of conversion of hydrated basic dicarboxylate aluminium(II I) complexes Al(OH)(succinate). xH(2)O and Al(OH)(adipate). xH(2)O to alumina and aluminium nitride (AIN) has been investigated by Al-27 mag ic angle spinning nuclear magnetic resonance (MAS NMR) spectroscopy. T he powdered succinate complex was calcined under various atmospheres s uch as N-2, argon and air. The Al-27 MAS NMR spectra for the calcined materials at 500 degrees C all showed three peaks at delta 6, 33 and 6 3. The relative intensities of these peaks varied with increasing temp erature and were also dependent on the calcination atmosphere. The Al- 27 NMR signal of AlN at delta 114 was observed for the sample calcined in an N-2 atmosphere at 1150 degrees C whilst in all spectra of sampl es calcined under an N-2 atmosphere at >1150 degrees C there were no d etectable signals other than those of gamma-alumina and AlN. The findi ng that the ratio of the relative intensities of AlO6 and AlO4 groups in gamma-alumina changes with temperature suggests that the carbotherm al reduction and nitridation of alumina proceeds through intermediates with empirical formulae of the type AlOxNy. The degree of nitridation at each reaction temperature for the succinate complex was higher tha n that for the adipate complex.