Issue 4, 1991

27Al nuclear magnetic resonance spectroscopy investigation of thermal transformation sequences of alumina hydrates. Part 1.—Gibbsite, γ-Al(OH)3

Abstract

High-resolution 27Al magic-angle spinning nuclear magnetic resonance spectroscopy (MAS NMR)(78.15 MHz) spectra are reported for commercial and natural gibbsites and materials occurring in the thermal transformation sequences of gibbsite (boehmite; χ, α and ρ-aluminas; calcines produced at 400, 700, 900 and 1000 °C). Separate peaks assignable to aluminiums in near-regular six- and four-co-ordination in oxygen are observed for the materials in which use of such sites is believed to occur. For ρ-alumina a third peak (at 27 ppm) is seen due to the presence of Al in five-co-ordination. κ-Alumina may retain approximately hexagonal-close-packed oxygens (with a defect structure leading to a grossly asymmetric contributory line from four-co-ordinate Al) or may contain some five-co-ordinate Al (AlO5) in addition to AlO6 and AlO4 environments (and hence have oxygen packing deviating from h.c.p.). Distortions/disorders (when present) result in broader underlying signals and manifest themselves instrumentally for the most disordered systems as wings extending to either side of the central spectrum.

Article information

Article type
Paper

J. Mater. Chem., 1991,1, 563-568

27 Al nuclear magnetic resonance spectroscopy investigation of thermal transformation sequences of alumina hydrates. Part 1.—Gibbsite, γ-Al(OH)3

R. C. T. Slade, J. C. Southern and I. M. Thompson, J. Mater. Chem., 1991, 1, 563 DOI: 10.1039/JM9910100563

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