Abstract

Electron spin resonance and electron spin echo modulation analysis are used to identify the location and coordination of Cu2+ in hydrated and dehydrated CaX zeolite. A new, trigonal bipyramidally coordinated Cu2+ is found to be the dominant copper center in this zeolite. It is located in a six ring window (site SII) and coordinated to three six ring oxygens and two hydroxyls, one in the α cage and the other in the β cage of the zeolite. This Cu(Oz)3(OH)2 species is found to be stable for dehydration up to 180 °C. At higher temperatures the Cu2+ species seems to be reduced irreversibly. However, a Cu2+ species can be regenerated by oxidation and hydration but most of it is only trigonally coordinated.

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