Titanium-exchanged zeolite systems

Titanium(III) exchanged 3A zeolite can also split water according to Eyring and coworkers (18). Illumination with visible light causes the evolution of h rogen as evidenced by mass spectrometry. As with the silver system described above, the titanium 3A zeolite process is not catalytic and loses reversibility. A detailed report concerning the electron paramagnetic resonance spectra of the titanium(III) 3A zeolite system has also been recently reported (19). 

The finding of an active solid redox system resulted in a flourish of activity in the development and application of diverse redox molecular sieves containing titanium (IV) and other metal ions [378-380]. Like the earlier ion-exchanged zeolites, many of the resulting catalysts, however, also suffered from loss by leaching, even when the redox element was substituted in the framework [102]. Ti-substituted zeolites remain special because of then stability. 

Because acidified titanium oxide is the catalyst usually employed commercially for the transformation of 1 into 2 [8] there has been much investigation of this catalytic system [9]. A 1995 paper by Stefanis et al. [10] reported an investigation of the reaction of 1 in several alumina-pillared clays (PILCs montmorillonite- and beidellite-based, and their and Ca" -exchanged congeners) under Lewis acid conditions (solid is activated by heat to remove all water). The results were compared with those obtained by use of medium-pore zeolites USY, NH4+-ZSM-5, and H-mordenite. Conversion to 2 > 50% was always observed. The aim of the work was to clarify differences between site availability and acidity for the two types of solid. 

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