The layer structured manganese titanate, RbxMnxTi2-xO(4) (x = 0.75) was pil
lared with decylammonium ions by the ion-exchange, and then, tetraethyl ort
hosilicate (TEOS) was hydrolyzed between pillared layers. On calcination, t
he alkylammonium ions were decomposed, and the hydrolyzed TEOS was in turn
changed into silica pillars, forming micropores between the layers. The amo
unt of silica formed was dependent on the amount of water contained in the
decylammonium pillared titanates. The specific surface area of the silica-p
illared structure increased linearly with the increase of the basal spacing
and the amount of silica introduced. This suggested that the interlayer sp
ace was filled with silica particles of nano- or subnano-meter sizes, which
were packed in a uniform way irrespective of the basal spacing. The microp
ores were formed between the packed silica particles.