EM - Escola de Minas

URI permanente desta comunidadehttp://www.hml.repositorio.ufop.br/handle/123456789/6

Notícias

A Escola de Minas de Ouro Preto foi fundada pelo cientista Claude Henri Gorceix e inaugurada em 12 de outubro de 1876.

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Resultados da Pesquisa

Agora exibindo 1 - 10 de 48
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    Assessment of the molecular structure of an intermediate member of the triplite-zwieselite mineral series : a raman and infrared study.
    (2014) Frost, Ray Leslie; Xi, Yunfei; López, Andrés; Moreira, Viviane Amaral; Cipriano, Ricardo Augusto Scholz; Lima, Rosa Malena Fernandes; Gandini, Antônio Luciano
    The mineral series triplite-zwieselite with theoretical formula (Mn2þ)2(PO4)(F)-(Fe2þ)2(PO4)(F) from the El Criolo granitic pegmatite, located in the Eastern Pampean Ranges of Cordoba Province, was studied using electron microprobe, thermogravimetry, and Raman and infrared spec- troscopy. The analysis of the mineral provided a formula of (Fe1.00, Mn0.85, Ca0.08, Mg0.06)P2.00(PO4)1.00(F0.80, OH0.20)P1.00. An intense Raman band at 981cm1 with a shoulder at 977cm1 is assigned to the PO3 4 n1 symmetric stretching mode. The observation of two bands for the phosphate symmetric stretching mode offers support for the concept that the phosphate units in the structure of triplite-zwieselite are not equivalent. Low-intensity Raman bands at 1012, 1036, 1071, 1087, and 1127 cm1 are assigned to the PO3 4 n3 antisymmetric stretching modes. A set of Raman bands at 572, 604, 639, and 684 cm1 are attributed to the PO3 4 n4 out-of-plane bending modes. A single intense Raman band is found at 3508 cm1 and is assigned to the stretching vibration of hydroxyl units. Infrared bands are observed at 3018, 3125, and 3358 cm1 and are attributed to water stretching vibrations. Supplemental materials are available for this article. Go to the publisher’s online edition of Spectroscopy Letters to view the supplemental file.
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    Thermal analysis and infrared emission spectroscopy of the borate mineral colemanite (CaB3O4(OH)3H2O) : implications for thermal stability.
    (2016) Frost, Ray Leslie; Cipriano, Ricardo Augusto Scholz; Ruan, Xiuxiu; Lima, Rosa Malena Fernandes
    Colemanite CaB3O4(OH)3H2O 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. We have studied the thermal decomposition of colemanite by using a combination of thermal analysis (TG/DTG) and infrared emission spectroscopy (IES). Thermogravimetric analysis of the colemanite mineral was obtained by using TA Instruments Inc. Q50 high-resolution TGA operating at a 10 C min-1 ramp with data sample interval of 0.50 s pt-1 from room temperature to 1000 C in a high-purity flowing nitrogen atmosphere (100 cm3 min-1 ). Thermogravimetric analysis shows a sharp mass loss at 400.9 C. Only a single mass loss is observed. IES shows a sharp band at 3610 cm-1 assigned to the stretching vibration of hydroxyl units. Intensity in this band is lost by 350 C. A broad spectral feature is observed at 3274 cm-1 attributed to water stretching vibrations. Intensity in this band is lost by 300 C. A combination of thermogravimetry and IES is used to study the thermal stability of the borate mineral colemanite. 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.
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    A Raman and infrared spectroscopic study of the phosphate mineral laueite.
    (2016) Frost, Ray Leslie; Cipriano, Ricardo Augusto Scholz; López, Andrés
    A laueite mineral sample from Lavra Da Ilha, Minas Gerais, Brazil has been studied by vibrational spectroscopy and scanning electron microscopy with EDX. Chemical formula calculated on the basis of semi-quantitative chemical analysis can be expressed as (Mn2+0.85,Fe2+0.10Mg0.05)P1.00(Fe3+1.90,Al0.10)P2.00(PO4)2(OH)2_8H2O. The laueite structure is based on an infinite chains of vertex-linked oxygen octahedra, with Fe3+ occupying the octahedral centers, the chain oriented parallel to the c-axis and linked by PO4 groups. Consequentially not all phosphate units are identical. Two intense Raman bands observed at 980 and 1045 cm_1 are assigned to the n1 PO43_ symmetric stretching mode. Intense Raman bands are observed at 525 and 551 cm_1 with a shoulder at 542 cm_1 are assigned to the n4 out of plane bending modes of the PO43_. The observation of multiple bands supports the concept of non-equivalent phosphate units in the structure. Intense Raman bands are observed at 3379 and 3478 cm_1 and are attributed to the OH stretching vibrations of the hydroxyl units. Intense broad infrared bands are observed. Vibrational spectroscopy enables subtle details of the molecular structure of laueite to be determined.
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    A SEM, EDS and vibrational spectroscopic study of the clay mineral fraipontite.
    (2015) Theiss, Frederick L.; López, Andrés; Cipriano, Ricardo Augusto Scholz; Frost, Ray Leslie
    The mineral fraipontite has been studied by using a combination of scanning electron microscopy with energy dispersive analysis and vibrational spectroscopy (infrared and Raman). Fraipontite is a member of the 1:1 clay minerals of the kaolinite-serpentine group. The mineral contains Zn and Cu and is of formula (Cu,Zn,Al)3(Si,Al)2O5(OH)4. Qualitative chemical analysis of fraipontite shows an aluminium silicate mineral with amounts of Cu and Zn. This kaolinite type mineral has been characterised by Raman and infrared spectroscopy; in this way aspects about the molecular structure of fraipontite clay are elucidated.
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    SEM, EDX, Infrared and Raman spectroscopic characterization of the silicate mineral yuksporite.
    (2015) Frost, Ray Leslie; López, Andrés; Cipriano, Ricardo Augusto Scholz; Theiss, Frederick L.; Romano, Antônio Wilson
    The mineral yuksporite (K,Ba)NaCa2(Si,Ti)4O11(F,OH) H2O has been studied using the combination of SEM with EDX and vibrational spectroscopic techniques of Raman and infrared spectroscopy. Scanning electron microscopy shows a single pure phase with cleavage fragment up to 1.0 mm. Chemical analysis gave Si, Al, K, Na and Ti as the as major elements with small amounts of Mn, Ca, Fe and REE. Raman bands are observed at 808, 871, 930, 954, 980 and 1087 cm 1 and are typical bands for a natural zeolite. Intense Raman bands are observed at 514, 643 and 668 cm 1. A very sharp band is observed at 3668 cm 1 and is attributed to the OH stretching vibration of OH units associated with Si and Ti. Raman bands resolved at 3298, 3460, 3562 and 3628 cm 1 are assigned to water stretching vibrations.
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    An SEM, EDS and vibrational spectroscopic study of the silicate mineral meliphanite (Ca,Na)2Be[(Si,Al)2O6(F,OH)].
    (2015) Frost, Ray Leslie; López, Andrés; Theiss, Frederick L.; Romano, Antônio Wilson; Cipriano, Ricardo Augusto Scholz
    The mineral meliphanite (Ca,Na)2Be[(Si,Al)2O6(F,OH)] is a crystalline sodium calcium beryllium silicate which has the potential to be used as piezoelectric material and for other ferroelectric applications. The mineral has been characterized by a combination of scanning electron microscopy (SEM) with energy dispersive spectroscopy (EDS) and vibrational spectroscopy. EDS analysis shows a material with high concentrations of Si and Ca and low amounts of Na, Al and F. Beryllium was not detected. Raman bands at 1016 and 1050 cm 1 are assigned to the SiO and AlOH stretching vibrations of three dimensional siloxane units. The infrared spectrum of meliphanite is very broad in comparison with the Raman spectrum. Raman bands at 472 and 510 cm 1 are assigned to OSiO bending modes. Raman spectroscopy identifies bands in the OH stretching region. Raman spectroscopy with complimentary infrared spectroscopy enables the characterization of the silicate mineral meliphanite.
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    A vibrational spectroscopic study of the phosphate mineral vantasselite Al4(PO4)3(OH)3 9H2O.
    (2015) Frost, Ray Leslie; Cipriano, Ricardo Augusto Scholz; Belotti, Fernanda Maria; López, Andrés; Theiss, Frederick L.
    We have studied the phosphate mineral vantasselite Al4(PO4)3(OH)3 9H2O using a combination of SEM with EDX and Raman and infrared spectroscopy. Qualitative chemical analysis shows Al, Fe and P. Raman bands at 1013 and 1027 cm 1 are assigned to the PO43 m1 symmetric stretching mode. The observation of two bands suggests the non-equivalence of the phosphate units in the vantasselite structure. Raman bands at 1051, 1076 and 1090 cm 1 are attributed to the PO43 m3 antisymmetric stretching vibration. A comparison is made with the spectroscopy of wardite. Strong infrared bands at 1044, 1078, 1092, 1112, 1133, 1180 and 1210 cm 1 are attributed to the PO4 3 m3 antisymmetric stretching mode. Some of these bands may be due to dAl2OH deformation modes. Vibrational spectroscopy offers a mechanism for the study of the molecular structure of vantasselite.
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    Raman and infrared spectroscopic study of turquoise minerals.
    (2015) Čejka, Jiři; Sejkora, Jiři; Macek, Ivo; Malíková, Radana; Wang, Lina; Cipriano, Ricardo Augusto Scholz; Xi, Yunfei; Frost, Ray Leslie
    Raman and infrared spectra of three well-defined turquoise samples, CuAl6(PO4)4(OH)8_4H2O, from Lavender Pit, Bisbee, Cochise county, Arizona; Kouroudaiko mine, Faleme river, Senegal and Lynch Station, Virginia were studied, interpreted and compared. Observed Raman and infrared bands were assigned to the stretching and bending vibrations of phosphate tetrahedra, water molecules and hydroxyl ions. Approximate O–H…O hydrogen bond lengths were inferred from the Raman and infrared spectra. No Raman and infrared bands attributable to the stretching and bending vibrations of (PO3OH)2_ units were observed.
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    A vibrational spectroscopic study of the silicate mineral pectolite – NaCa2Si3O8(OH).
    (2015) Frost, Ray Leslie; López, Andrés; Theiss, Frederick L.; Romano, Antônio Wilson; Cipriano, Ricardo Augusto Scholz
    The mineral pectolite NaCa2Si3O8(OH) is a crystalline sodium calcium silicate which has the potential to be used in plaster boards and in other industrial applications. Raman bands at 974 and 1026 cm 1 are assigned to the SiO stretching vibrations of linked units of Si3O8 units. Raman bands at 974 and 998 cm 1 serve to identify Si3O8 units. The broad Raman band at around 936 cm 1 is attributed to hydroxyl deformation modes. Intense Raman band at 653 cm 1 is assigned to OSiO bending vibration. Intense Raman bands in the 2700–3000 cm 1 spectral range are assigned to OH stretching vibrations of the OH units in pectolite. Infrared spectra are in harmony with the Raman spectra. Raman spectroscopy with complimentary infrared spectroscopy enables the characterisation of the silicate mineral pectolite.
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    A vibrational spectroscopic study of the copper bearing silicate mineral luddenite.
    (2015) Frost, Ray Leslie; López, Andrés; Xi, Yunfei; Cipriano, Ricardo Augusto Scholz
    The molecular structure of the copper–lead silicate mineral luddenite has been analysed using vibrational spectroscopy. The mineral is only one of many silicate minerals containing copper. The intense Raman band at 978 cm 1 is assigned to the m1 (A1g) symmetric stretching vibration of Si5O14 units. Raman bands at 1122, 1148 and 1160 cm 1 are attributed to the m3 SiO4 antisymmetric stretching vibrations. The bands in the 678–799 cm 1 are assigned to OSiO bending modes of the (SiO3)n chains. Raman bands at 3317 and 3329 cm 1 are attributed to water stretching bands. Bands at 3595 and 3629 cm 1 are associated with the stretching vibrations of hydroxyl units suggesting that hydroxyl units exist in the structure of luddenite.