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Optical absorption, luminescence, and electron paramagnetic resonance (EPR) spectroscopy of crystalline to metamict zircon: Evidence for formation of uranyl, manganese, and other optically active centers

机译:晶体到半锆石的光学吸收,发光和电子顺磁共振(EPR)光谱:形成铀酰,锰和其他旋光中心的证据

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摘要

A spectroscopic study on seven natural zircon crystals representing varying coloration and degree of short-range order has been conducted using Raman, optical absorption (OA), time-resolved laser-induced luminescence (TRL), and electron paramagnetic resonance (EPR) spectroscopy. There is a systematic increase in the line width of the central Gd3+ transition in the EPR spectra with decreasing short-range order as defined by Raman spectroscopy. In the luminescence spectra, the broad-band yellow photoluminescence centered at about 560 nm is restricted to samples with a high degree of short-range order. In contrast, photoluminescence related to trivalent rare earth elements was detected in zircon with both intermediate and high degrees of short-range order, but not in one heterogeneous, intermediate to highly metamict sample. Furthermore, short-lived greenish luminescence, typical of uranyl ions, could be detected in the luminescence spectra of partly and strongly metamict zircon. Reabsorption lines related to the presence of tetravalent U were found in luminescence spectra of both well-ordered and metamict samples. These observations give evidence for the occurrence of hexavalent U, besides the tetra- and pentavalent forms in natural zircon. It appears that pentavalent U initially present in crystalline zircon converted to tetra- and hexavalent U in highly metamict samples. For a well-ordered green zircon crystal from Caldas Minas, Minas Gerais (Brazil), spectra of Mn2+ (or Mn4+) were detected by both EPR and luminescence spectroscopy, demonstrating that Mn centers may be present in this mineral. Potential color centers are discussed. Green coloration of natural zircon cannot be assigned exclusively to the presence of U4+ as suggested previously. Furthermore, no significant influence of the Nb4+ center on zircon coloration, including reddish color, was found. Yellow coloration may be related to the absorption due to charge-transfer bands of Pr4+.
机译:变色和短程有序度的七种天然锆石晶体的光谱学研究已经通过拉曼,光学吸收(OA),时间分辨进行了激光诱导发光(TRL)和电子顺磁 共振(EPR)光谱。 EPR 光谱中中心Gd 3 + 跃迁的线宽有系统的增加 ,短距离顺序由拉曼 光谱学。在发光光谱中,以约560 nm为中心的宽带黄 光致发光仅限于具有高度短程有序度的 样品。相反,在锆石中检测到与三价稀土元素有关的 光致发光,其中 具有短距离的中度和高度,但没有一种异质的,中间的 到高度置换样品。此外,在部分和强半金属锆石的 发光光谱中,可以检测到典型的铀酰离子的短时绿色 发光。 重吸收线在有序和 metamict样品的发光光谱中发现了与四价U 的存在有关的信息。这些观察结果为 天然锆石中的四价和五价形式的六价铀提供了证据。看来五价U最初存在于 晶体锆石中,并转化为 高取代度样品中的四价和六价U。对于来自Minas Gerais(巴西)的Caldas Minas的有序绿色锆石晶体 ,Mn 2 + (或 Mn 通过EPR和发光光谱检测到4 + ), 表明该矿物质中可能存在Mn中心。如前所述,天然 锆石的绿色不能专门分配给存在U 4 + 的锆石。此外,未发现Nb 4 + 中心对锆石着色(包括带红色) 有显着影响。黄色可能与Pr 4 + 的电荷转移带有关。

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  • 来源
    《American Mineralogist》 |2010年第3期|335-347|共13页
  • 作者单位

    Institut für Mineralogie, TU Bergakademie Freiberg, Brennhausgasse 14, 09596 Freiberg, Germany;

    Institut für Mineralogie, TU Bergakademie Freiberg, Brennhausgasse 14, 09596 Freiberg, Germany|Helmholtz Centre Potsdam, GFZ German Research Centre for Geosciences, Telegrafenberg D320, 14473 Potsdam, Germany;

    Institut für Radiochemie, Forschungszentrum Dresden-Rossendorf, P.O. 510119, 01314 Dresden, Germany;

    Helmholtz Centre Potsdam, GFZ German Research Centre for Geosciences, Telegrafenberg D320, 14473 Potsdam, Germany;

    Institute for Geotechnical Engineering, ETH Zurich, Schafmattstrasse 6, 8093 Zurich, Switzerland;

    Fakult?t für Physik und Geowissenschaften, Universit?t Leipzig, Linnéstrasse 5, 04103 Leipzig, Germany;

    Institut für Radiochemie, Forschungszentrum Dresden-Rossendorf, P.O. 510119, 01314 Dresden, Germany;

    Fakult?t für Physik und Geowissenschaften, Universit?t Leipzig, Linnéstrasse 5, 04103 Leipzig, Germany;

    alpha Geoservice GbR, Talstrasse 29, 09627 Bobritzsch, Germany;

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