Abstract

Solid state 27Al and 29Si NMR was used to examine the structures of aluminosilicates and sodium aluminosilicates prepared by the sol-gel method from metal alkoxides. In contrast to the borosilicate system, where B-O-Si bonds are not formed until heat treatment above 150° C, Al-O-Si formation appears complete upon gelation. Aluminium occupies tetrahedral [AlO4]− sites in the polymer network and octahedral [Al(H2O)6]3+ (or similar) sites in the intersticies for charge balance. When sodium is added as a counter ion the octahedral aluminium is converted to tetrahedral aluminium in the oxide network. In gels of high aluminium content prepared from (BusO)2Al-O-Si(OEt)3, some aluminium in five coordinate environments is also observed. All gels remain amorphous on heating to 800° C.

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