The hexagonal structure of the mesostructured silica nanoparticles (MSN) based solid acid catalyst was synthesized using 1,2-propanediol as a co-solvent by sol-gel method, followed by aluminum grafting and protonation. The activity of the catalysts was tested for cumene conversion in a pulse microcatalytic reactor at 323-573 K. XRD, TEM and N-2 physisorption results confirmed the hexagonal ordered structure with a pore diameter of 3.4-4.0 nm, a particle size of 70-120 nm and a surface area of 588-995 m(2)/g. Solid state NMR and IR results confirmed that the aluminum grafting and protonation form framework and extra-framework aluminums which led to generating strong Bronsted and Lewis acidic sites. High activity in the cumene conversion was only observed on HAIMSN producing propylene, benzene, toluene via a cracking on protonic acid sites and producing a main product of alpha-methylstyrene via a dehydrogenation on Lewis acidic sites at high reaction temperature. While only alpha-methylstyrene and higher hydrocarbon ( >= C-10) were produced at low reaction temperature showing the permanent Bronsted acid sites did not involve in the cumene conversion. It is suggested that the presence of hydrogen and strong Lewis acid sites increased the stability and activity of the HAIMSN catalyst in the cumene conversion. Although the small deactivation of HAIMSN was observed during the reaction due to the formation of small coke deposits on the surface, the reactivation recovered the activity of catalyst and the high activity was still observed after 60 h of reaction. The high stability and activity of HAIMSN in the cumene conversion can be considered as a method for the production of alpha-methylstyrene via a dehydrogenation process. (C) 2013 Elsevier B.V. All rights reserved.