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Phosphorescence emission zeolites

Marquez, F., Marti, V., Palomares, E., Garcia, H. and Adam, W. (2002). Observation of azo chromophore fluorescence and phosphorescence emissions from DBH by applying exclusively the orbital confinement effect in siliceous zeolites devoid of charge-balancing cations. J. Am. Chem. Soc. 124, 7264-7265... [Pg.262]

Based on steady-state and time-resolved emission studies, Scaiano and coworkers have concluded that silicalite (a pentasil zeolite) provides at least two types of sites for guest molecules [234-236], The triplet states of several arylalkyl ketones and diaryl ketones (benzophenone, xanthone, and benzil) have been used as probes. Phosphorescence from each molecule included in silicalite was observed. With the help of time-resolved diffuse reflectance spectroscopy, it has been possible to show that these triplet decays follow complex kinetics and extend over long periods of time. Experiments with benzophenone and arylalkyl ketones demonstrate that some sites are more easily accessed by the small quencher molecule oxygen. Also, diffuse reflectance studies in Na + -X showed that diphenylmethyl radicals in various sites decay over time periods differing by seven orders of magnitude (t varies between 20/is and 30 min) [237]. [Pg.157]

Europium(III) exchanged zeolites have been studied by a number of research groups. Arakawa and coworkers (20, 21 ) report the luminescence properties of europium(III)-exchanged zeolite Y. Emission spectra were measured under a variety of conditions and bands for europium(II) were observed after thermal treatment of the europium(III) Y zeolites. A mechanism was proposed for the thermal splitting of water which involved the cycling of europium between the two different oxidation states. Europium MSssbauer experiments (22 ) also show that on thermal treatment of europium-(III) zeolites that europium(II) is formed. Stucky and coworkers (23, 24) studied the phosphorescence lifetime of these europium-(lll) zeolites and showed that the inverse of the lifetime (the decay constant) was linearly related to the number of water molecules surrounding the europium(III) ion in the zeolite supercages. These studies involved zeolites A, X, Y and ZSM-5. [Pg.226]

The Nph molecules adsorbed from a solution in hexane on the NaX zeolite surface exhibite a strong emission consisting of structured fluorescence and phosphorescence and an additional structureless band with a peak at 400 ntn (Fig.l). The vibrational analysis of the structural spectra is presented in Table 1. [Pg.608]

The spectrum of Nph form on aerosil is not resolved. The wide-band fluorescence contribution relative to the molecular emission is large, afterglow is not observed. The wideband excitation spectrum at 400 nm is shifted relatively to that of a molecular form by 10 nm. For zeolites this is mainly CTC and for aerosil a bimolecular associate of Nph. When adsorbing from a vapor phase, the emission spectrum of Nph in a zeolite consists of a continuous structureless band which is a superposition of CTC and dimers adsorbed at the outer surface (Fig. 3a).In the case of co-adsorption of water vapor or hexane the spectrum transforms with the appearance of structured fluorescence and phosphorescence components (Fig.3b). The coadsorbate seems to promote breaking up of dimers and diffusion of molecules in zeolite cages. [Pg.609]


See other pages where Phosphorescence emission zeolites is mentioned: [Pg.170]    [Pg.1885]    [Pg.163]    [Pg.612]    [Pg.328]   
See also in sourсe #XX -- [ Pg.218 , Pg.221 ]




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