H-ferrierite was treated with oxalic acid to selectively remove extern
al acid sites. The treatment led to the reduction of tetrahedrally coo
rdinated aluminum ions and the increase of octahedrally coordinated al
uminum species and micropore surface area. It was also found that the
catalyst treated with oxalic acid is resistant to coking. Over modifie
d H-FER, very high selectivity to isobutene is obtained at lower conve
rsions suggesting the skeletal isomerization of I-butene is occurring
through a mono-molecular reaction mechanism.