DEGEO - Departamento de Geologia

URI permanente desta comunidadehttp://www.hml.repositorio.ufop.br/handle/123456789/8

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    The molecular structure of the borate mineral szaibelyite MgBO2(OH) : a vibrational spectroscopic study.
    (2015) Frost, Ray Leslie; Cipriano, Ricardo Augusto Scholz; López, Andrés; Belotti, Fernanda Maria
    We have studied the borate mineral szaibelyite MgBO2(OH) using electron microscopy and vibrational spectroscopy. EDS spectra show a phase composed of Mg with minor amounts of Fe. Both tetrahedral and trigonal boron units are observed. The nominal resolution of the Raman spectrometer is of the order of 2 cm 1 and as such is sufficient enough to identify separate bands for the stretching bands of the two boron isotopes. The Raman band at 1099 cm 1 with a shoulder band at 1093 cm 1 is assigned to BO stretching vibration. Raman bands at 1144, 1157, 1229, 1318 cm 1 are attributed to the BOH in-plane bending modes. Raman bands at 836 and 988 cm 1 are attributed to the antisymmetric stretching modes of tetrahedral boron. The infrared bands at 3559 and 3547 cm 1 are assigned to hydroxyl stretching vibrations. Broad infrared bands at 3269 and 3398 cm 1 are assigned to water stretching vibrations. Infrared bands at 1306, 1352, 1391, 1437 cm 1 are assigned to the antisymmetric stretching vibrations of trigonal boron. Vibrational spectroscopy enables aspects of the molecular structure of the borate mineral szaibelyite to be assessed.
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    Vibrational spectroscopy of the mineral meyerhofferite CaB3O3(OH)5 H2O - an assessment of the molecular structure.
    (2013) Frost, Ray Leslie; López, Andrés; Xi, Yunfei; Cipriano, Ricardo Augusto Scholz; Costa, Geraldo Magela da; Belotti, Fernanda Maria; Lima, Rosa Malena Fernandes
    Meyerhofferite is a calcium hydrated borate mineral with ideal formula: CaB3O3(OH)5_H2O and occurs as white complex acicular to crude crystals with length up to _4 cm, in fibrous divergent, radiating aggregates or reticulated and is often found in sedimentary or lake-bed borate deposits. The Raman spectrum of meyerhofferite is dominated by intense sharp band at 880 cm_1 assigned to the symmetric stretching mode of trigonal boron. Broad Raman bands at 1046, 1110, 1135 and 1201 cm_1 are attributed to BOH in-plane bending modes. Raman bands in the 900–1000 cm_1 spectral region are assigned to the antisymmetric stretching of tetrahedral boron. Distinct OH stretching Raman bands are observed at 3400, 3483 and 3608 cm_1. The mineral meyerhofferite has a distinct Raman spectrum which is different from the spectrum of other borate minerals, making Raman spectroscopy a very useful tool for the detection of meyerhofferite in sedimentary and lake bed deposits.
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    Infrared and Raman spectroscopic characterization of the borate mineral colemanite CaB3O4(OH)3 H2O - implications for the molecular structure.
    (2013) Frost, Ray Leslie; Xi, Yunfei; Cipriano, Ricardo Augusto Scholz; Belotti, Fernanda Maria; Cândido Filho, Mauro
    Colemanite CaB3O4(OH)3_H2O is a secondary borate mineral formed from borax and ulexite in evaporate deposits of alkaline lacustrine sediments. The basic structure of colemanite contains endless chains of interlocking BO2(OH) triangles and BO3(OH) tetrahedrons with the calcium, water and extra hydroxide units interspersed between these chains. The Raman spectra of colemanite is characterized by an intense band at 3605 cm_1 assigned to the stretching vibration of OH units and a series of bands at 3182, 3300, 3389 and 3534 cm_1 assigned to water stretching vibrations. Infrared bands are observed in similar positions. The BO stretching vibrations of the trigonal and tetrahedral boron are characterized by Raman bands at 876, 1065 and 1084 cm_1. The OBO bending mode is defined by the Raman band at 611 cm_1. It is important to characterize the very wide range of borate minerals including colemanite because of the very wide range of applications of boron containing minerals.