Sites solid state

Measuring the acidity of the Bronsted and Lewis acid sites is problematic. The adsorption and desorption of various amines has been used, but there is some disagreement about what it means.160 Some workers prefer to use isopropylamine, which desorbs only from Bronsted sites. Solid-state nuclear magnetic resonance (NMR) has also been used in the study of reactions on zeolites.161 Many zeolites crystallize into crystals that are too fine for conventional X-ray analysis. A new method that uses synchrotron X rays on microcrystalline powders promises to make it much easier to determine the structures of zeolites and related materials.162... 

D. R. Franceschetti and P. C. Shipe [1984] Bulk Conductivity and Polarization of Ionic Crystals Exhibiting Defect Exchange between Inequivalent Sites, Solid State Ionics 11, 285-291. 

The BET treatment is based on a kinetic model of the adsorption process put forward more than sixty years ago by Langmuir, in which the surface of the solid was regarded as an array of adsorption sites. A state of dynamic equilibrium was postulated in which the rate at which molecules arriving from the gas phrase and condensing on to bare sites is equal to the rate at which molecules evaporate from occupied sites. 

Figure 5 Solid state NMR spectra of Vanadium oxide on y-alumina as a function of vanadium loading (wt.%) and surface coverage 0. Note the gradual emergence of the six-coordinated vanadium site with increased loading.

The final step of the whole reaction process is the desorption of the products. This step is essential not only for the practical purpose of collecting and storing the desired output, but also for the regeneration of the catalytic active sites of the surface. Most reactions have at least one rate-hmiting step, which frequently makes the reaction prohibitively slow for practical purposes when, e.g., it is intended for homogeneous (gas or fluid) media. The role of a good solid-state catalyst is to obtain an acceptable... 

The rate of isotopic exchange in the solid state, between cobalt in the cation and in the anion of [60Co(H2O)6] [Co(edta)]2 4 H20, was increased [1144] by irradiation (100 Mrad) of the reactant. It was concluded that exchange occurred via vacancies, rather than through motion of a ring of cobalt atoms, one from a cationic site and the other from a neighbouring anionic site. 

The radical anions of dialkyl sulfoxides (or sulfones) may be obtained by direct capture of electron during y-irradiation. It was shown that electron capture by several electron acceptors in the solid state gave anion adducts 27. It was concluded276 that these species are not properly described as radical anions but are genuine radicals which, formed in a solid state cavity, are unable to leave the site of the anions and exhibit a weak charge-transfer interaction which does not modify their conformation or reactivity appreciably, but only their ESR spectra. For hexadeuteriodimethyl sulfoxide in the solid state, electron capture gave this kind of adduct 278,28 (2H isotopic coupling 2.97 G is less than 3.58 G normally found for -CD3). 

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