Transformation of limonene into p-cymene over acid activated natural mordenite utilizing atmospheric oxygen as a green oxidant: A novel mechanism.

Natural mordenite originated from volcanic soils in Greek islands was treated with sulfuric acid aqueous solutions of different concentrations and solid mass/solution volumes. The samples were characterized using various techniques (N 2 -physisorption, XRD, ATR-FTIR, SEM-EDS, TEM, Microelectrophoresis, Equilibrium pH) and tested in the transformation of limonene into p -cymene in the presence of atmospheric air at various temperatures and reaction times. The acid treatment is causing the removal of sodium oxide located inside the framework micropores and the small inter-fiber mesopores. This, in turn, increases drastically the BET specific surface area and unmasks negatively charged surface sites which are transformed into acid sites by adsorbing H + /H 2 O + ions. The relatively low extent removal of Al 3+ ions does not disturb the framework of natural mordenite nor its fibrous morphology. The development of micropores and small mesopores surface area and surface acid sites are transforming the catalytically inactive natural mordenite into very active catalysts. The increase in the conversion and the yield of p -cymene follows the increase in the BET specific surface area. A novel mechanism was experimentally established involving a catalytic step followed by a non catalytic one. The first step involves adsorption of limonene on acid sites via the exocyclic double bond to form the more stable tertiary carbenium ion from which terpinolenes, terpinenes and “polymeric species” are formed. The “transition state shape selectivity” manifested by the catalysts studied does not allow the formation of intermediate disproportionation products. In the second step, catalyst-free aromatization and “polymerization” of terpinolenes and terpinenes were found to occur. The aromatization was proposed to proceed by abstraction of an allylic hydrogen resulting to free radical (R ) followed by combination with O 2 and radical chain propagation to yield allylic peroxides ([ROO ]) which by elimination of (HOO ) lead to the production of p -cymene. Moreover, high molecular weight compounds may be formed as radicals are combined to alkyl and peroxyl dimmers that may be polymerized. The experimental parameters concerning the acid treatment and reaction conditions were optimized for maximizing the amount of the produced p -cymene keeping as low as possible the amount of the produced polymeric species. [ABSTRACT FROM AUTHOR]