High
dimensionally structured niobium oxide (HDS-NbO) containing
fluoride (F–) was prepared by a hydrothermal synthesis.
F– could be introduced into HDS-NbO by replacing
lattice oxygen up to a solid F–/Nb ratio of 0.55.
The introduction of an appropriate amount of F– promoted
the crystal growth of HDS-NbO, while niobium oxyfluoride having the
hexagonal tungsten bronze structure (HTB-Nb(F,O)
x
) was concomitantly formed by excess F– addition.
HAADF-STEM analysis suggested that the number of micropores (hexagonal
and heptagonal channels) in HDS-NbO was increased by the introduction
of an appropriate amount of F–. The catalytic activity
for Brønsted acid reactions was evaluated by Friedel–Crafts
alkylation. The catalytic activity was significantly increased by
the introduction of F–, while excess introduction
of F– significantly decreased the activity. Catalytic
activity for the Lewis acid reaction in the presence of water was
evaluated by the transformation of pyruvaldehyde into lactic acid.
The catalytic activity was changed by the introduction of F– in a manner similar to that observed in the Friedel–Crafts
alkylation. On the basis of the results obtained, we propose that
the local catalyst structure around the micropores of HDS-NbO is crucial
for the acid reactions.