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O nuclear magnetic resonance study of Na2O-P2O5 glasses
Authors:Michaela ZeyerLionel Montagne  Valérie KostojGerard Palavit  Daniel ProchnowChristian Jaeger
Institution:a Institute of Optics and Quantum Electronics, Friedrich Schiller University of Jena, Max-Wien-Platz 1, D-07743 Jena, Germany
b Laboratoire de cristallochimie et Physicochimie du solide, UPRESA CNRS 8012, Ecole Nationale Superieure de Chimie de Lille, BP107, F-59652 Villeneuve d’Ascq, France
c Institute for Experimental Physics I, University of Leipzig, Linnéstr. 5, D-04103 Leipzig, Germany
d Federal Institute for Material Research and Testing, Richard-Willstaedter Str. 11, D-12489 Berlin, Germany
Abstract:The preparation and structural investigation of 17O-enriched xNa2O-(100−x)P2O5 glasses (46.5?x?62.8) by nuclear magnetic resonance (NMR) is described. Enriched phosphoric acid was prepared by hydrolysis of PCl5 with 17O-enriched water and neutralized with sodium carbonate. The sodium metaphosphate was then melted at 800 °C for 15 h and quenched. Polyphosphate and ultraphosphate glass compositions were prepared by remelting the metaphosphate with sodium carbonate and phosphorus pentoxide, respectively. 31P magic angle sample spinning (MAS) NMR was used to determine the Na2O/P2O5 content in the glasses. 17O NMR spectra (quadrupole echo for non-rotating samples and multiple-quantum excitation for rotating samples (MQMAS)) show two oxygen sites in the samples with large quadrupolar coupling constants (4.7 and 7.7 MHz), in accordance with the high phosphorus electronegativity. According to the correlation of 17O quadrupolar constants with bond ionicity, these two components are attributed to bridging P-O-P and non-bridging P-O?Na oxygens. The average P-O-P bond angle is estimated with the quadrupolar asymmetry derived from the fit of the static echo spectra. The MQMAS spectrum shows a distribution of non-bridging oxygen chemical shifts, attributed to a variation of bond length and angle.
Keywords:N220  P147
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