A vibrational spectroscopic study of the anhydrous phosphate mineral sidorenkite Na3Mn(PO4)(CO3)

被引:9
作者
Frost, Ray L. [1 ]
Lopez, Andres [1 ]
Scholz, Ricardo [2 ]
Belotti, Fernanda Maria [3 ]
Xi, Yunfei [1 ]
机构
[1] Queensland Univ Technol, Fac Sci & Engn, Sch Chem Phys & Mech Engn, Brisbane, Qld 4001, Australia
[2] Univ Fed Ouro Preto, Sch Mines, Dept Geol, BR-3540000 Ouro Preto, MG, Brazil
[3] Univ Fed Itajuba, Itabira, MG, Brazil
基金
澳大利亚研究理事会;
关键词
Sidorenkite; Phosphate; Carbonate; Raman spectroscopy; Infrared spectroscopy; KOLA-PENINSULA; RUSSIA;
D O I
10.1016/j.saa.2014.08.029
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
Sidorenkite is a very rare low-temperature hydrothermal mineral, formed very late in the crystallization of hyperagpaitic pegmatites in a differentiated alkalic massif (Mt. Alluaiv, Kola Peninsula, Russia). Sidorenkite Na3Mn(PO4)(CO3) is a phosphate-carbonate of sodium and manganese. Such a formula with two oxyanions lends itself to vibrational spectroscopy. The sharp Raman band at 959 cm(-1) and 1012 cm-1 are assigned to the PO43- stretching modes, whilst the Raman bands at 1044 cm(-1) and 1074 cm(-1) are attributed to the CO32- stretching modes. It is noted that no Raman bands at around 800 cm(-1) for sidorenkite were observed. The infrared spectrum of sidorenkite shows a quite intense band at 868 cm(-1) with other resolved component bands at 850 and 862 cm(-1). These bands are ascribed to the CO32- out-of-plane bend (v(2)) bending mode. The series of Raman bands at 622, 635, 645 and 704 cm(-1) are assigned to the v(4) phosphate bending modes. The observation of multiple bands supports the concept of a reduction in symmetry of the carbonate anion from D-3h or even C-2v. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:930 / 934
页数:5
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