Abstract

A gamma-irradiated synthetic B-type carbonated apatite calcined at 300°C was studied by EPR and ENDOR. The room temperature EPR spectrum is composed of an axially symmetric species (g⊥=2.0025 and g‖=1.9971) attributed to rotating CO2− radicals. At low temperatures (T<10 K), the CO2−1H and 31P ENDOR spectra were obtained for different magnetic field settings. Computer simulations of these ENDOR spectra, based on the ‘‘molecular orientation–selection’’ principle, enabled one to allocate the CO2− radicals in the carbonated apatite lattice. It was established that the CO2− radicals are located on PO43− sites with a vacancy on the nearest OH− site. In addition, discussions related to the substitution mechanisms and the nature of the precursors of the CO2− radicals are presented.

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