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Título : Raman and infrared spectroscopic characterization of the arsenate-bearing mineral tangdanite– and in comparison with the discredited mineral clinotyrolite.
Autor : Frost, Ray Leslie
Cipriano, Ricardo Augusto Scholz
López, Andrés
Palabras clave : Tangdanite
Arsenate
Raman spectroscopy
Sulphate
Fecha de publicación : 2013
Citación : FROST, R. L.; CIPRIANO, R. A. S.; LÓPES, A. Raman and infrared spectroscopic characterization of the arsenate-bearing mineral tangdanite – and in comparison with the discredited mineral clinotyrolite. Spectroscopy Letters, v. 46, p. 920–926, 2013. Disponível em: <https://onlinelibrary.wiley.com/doi/full/10.1002/jrs.4691>. Acesso em: 20 jun. 2017.
Resumen : Theminerals clinotyrolite and fuxiaotuite are discredited in terms of the mineral tangdanite. Themixed anionmineral tangdanite Ca2Cu9(AsO4)4(SO4)0.5(OH)9 9H2O has been studied using a combination of Raman and infrared spectroscopy. Characteristic bands associated with arsenate, sulphate and hydroxyl units are identified. Broad bands in the OH stretching region are observed and are resolved into component bands. These bands are assigned to water and hydroxyl stretching vibrations. Two intense Raman bands at 837 and approximately 734 cm 1 are assigned to the ν1 (AsO4)3 symmetric stretching and ν3 (AsO4)3 antisymmetric stretching modes. Infrared bands at 1023 cm 1 are assigned to the (SO4)2 ν1 symmetric stretching mode, and infrared bands at 1052, 1110 and 1132 cm 1 assigned to (SO4)2 ν3 antisymmetric stretching modes, confirming the presence of the sulphate anion in the tangdanite structure. Raman bands at 593 and 628 cm 1 are attributed to the (SO4)2 ν4 bending modes. Low-intensity Raman bands found at 457 and 472cm 1 are assigned to the (AsO4)3 ν2 bending modes. A comparison is made with the previously obtained spectral data on the discredited mineral clinotyrolite.
URI : http://www.repositorio.ufop.br/handle/123456789/8312
metadata.dc.identifier.uri2: https://onlinelibrary.wiley.com/doi/full/10.1002/jrs.4691
metadata.dc.identifier.doi: https://doi.org/10.1080/10426507.2012.761985
ISSN : 0038-7010
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