Journal
SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY
Volume 127, Issue -, Pages 237-242Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.saa.2014.02.067
Keywords
Phosphohedyphane; Hedyphane; Phosphate; Arsenate; Hydroxyl; Raman spectroscopy
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Funding
- Discipline of Nanotechnology and Molecular Science, Science and Engineering Faculty of the Queensland University of Technology
- Australian Research Council (ARC)
- CNPq - Conselho Nacional de Desenvolvimento Cientifico e Tecnologico [306287/2012-9, 402852/2012-5]
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Phosphohedyphane Ca2Pb3(PO4)(3)Cl is rare Ca and Pb phosphate mineral that belongs to the apatite supergroup. We have analysed phosphohedyphane using SEM with EDX, and Raman and infrared spectroscopy. The chemical analysis shows the presence of Pb, Ca, P and Cl and the chemical formula is expressed as Ca2Pb3(PO4)(3)Cl. The very sharp Raman band at 975 cm(-1) is assigned to the PO43- nu(1) symmetric stretching mode. Raman bands noted at 1073, 1188 and 1226 cm(-1) are to the attributed to the PO43- nu(3) antisymmetric stretching modes. The two Raman bands at 835 and 812 cm(-1) assigned to the AsO43- nu(1) symmetric stretching vibration and AsO43- nu(3) antisymmetric stretching modes prove the substitution of As for P in the structure of phosphohedyphane. A series of bands at 557, 577 and 595 cm-1 are attributed to the nu(4) out of plane bending modes of the PO4 units. The multiplicity of bands in the nu(2), nu(3) and nu(4) spectral regions provides evidence for the loss of symmetry of the phosphate anion in the phosphohedyphane structure. Observed bands were assigned to the stretching and bending vibrations of phosphate tetrahedra. Some Raman bands attributable to OH stretching bands were observed, indicating the presence of water and/or OH units in the structure. (C) 2014 Elsevier B.V. All rights reserved.
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