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首页> 外文期刊>American Mineralogist >Crystal structure of protoanthophyllite: A new mineral from the Takase ultramafic complex, Japan
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Crystal structure of protoanthophyllite: A new mineral from the Takase ultramafic complex, Japan

机译:原生质石的晶体结构:日本高濑超镁铁质复合物中的一种新矿物

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Protoanthophyllite, (Mg, Fe)7Si8O22(OH)2, is a newly discovered amphibole species from the Takase ultramafic complex in Japan. It occurs as prismatic crystals up to 5 mm in length in a thermally altered serpentinite that experienced contact metamorphism. The protoanthophyllite is associated with forsterite, talc, serpentine minerals, chlorite, chromian spinel, magnetite, pentlandite, and calcite. Some protoanthophyllite crystals contain minute lamellae of anthophyllite, other pyriboles, or both. Protoanthophyllite is biaxial negative, with refractive indices n = 1.593(2), nβ (calc.) = 1.609, n = 1.615(2), and 2Vx = 64(5)°. Electron microprobe analyses give an empirical formula of (Mg6.31Fe0.61Na0.06Mn0.01Ni0.01) 7.00(Si7.90Al0.14) 8.04O22(OH)2. It is orthorhombic with space group Pnmn. The unit-cell dimensions are a = 9.3553(8), b = 17.9308(15), and c = 5.3117(4) Å: with V = 891.0(3) Å3 and Z = 2. A single-crystal X-ray structure determination shows that, following the convention of Thompson (1981), protoanthophyllite has an (X) configuration. The topology of the silicate tetrahedral chains is similar to that of the anthophyllite A-chains. Silicate tetrahedral chains are O-rotated in protoanthophyllite, whereas those in protoferro-anthophyllite are S-rotated. Iron atoms are concentrated in the 4-coordinated M4 sites. The unit-cell volume is ~1.5% larger than the equivalent volume of anthophyllite with Mg/(Mg + Fe) = 0.885, suggesting a high-temperature or low-pressure stability relative to anthophyllite, assuming that protoanthophyllite is not metastable.
机译:原生质石(Mg,Fe) 7 Si 8 O 22 (OH) 2 是新发现的<来自日本高濑超镁铁质复合物的安瓿> 闪石。它以热变态蛇纹石的形式出现,长至5 mm,是棱柱状晶体,经历了接触变质作用。 原花石质与镁橄榄石,滑石, 蛇纹石矿物,绿泥石,铬尖晶石,磁铁矿,五芒石, 和方解石有关。某些原生叶蜡石晶体包含直闪石的微小 薄片,其他吡唑或两者兼有。 Protoanthophyllite 是双轴负值,折射率n = 1.593(2),n β (计算)= 1.609,n = 1.615(2),2Vx = 64(5)°。电子 微探针分析给出了(Mg 6.31 Fe 0.61 Na 0.06 Mn 0.01 Ni 0.01 7.00 (Si 7.90 Al 0.14 8.04 O 22 (OH) 2 。它是正交的,具有空间 group Pnmn。晶胞尺寸为a = 9.3553(8),b = 17.9308(15)和c = 5.3117(4)Å:V = 891.0(3)Å 3 且Z =2。单晶X射线结构确定表明 遵循汤普森(Thompson,1981)的惯例,原生质石 具有(X)配置。硅酸盐四面体 链的拓扑与直闪石A链的拓扑相似。硅酸 四面体链在原角质石中呈O-旋转,而 在原铁质角质石中呈S-旋转。铁原子 集中在4个配位的M4位。 Mg /(Mg + Fe)= 0.885时,单位晶格 体积比直闪石 的当量体积大约1.5%,这表明高温或 相对于直闪石的低压稳定性,假设 原叶蜡石不是亚稳态的。

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  • 来源
    《American Mineralogist 》 |2003年第12期| 00001718-00001723| 共6页
  • 作者单位

    Department of Geological Sciences, Arizona State University, Tempe, Arizona 85287-1404, U.S.A.;

    Department of Chemistry/Biochemistry, Arizona State University, Tempe, Arizona 85287-1604, U.S.A.;

    Department of Chemistry/Biochemistry, Arizona State University, Tempe, Arizona 85287-1604, U.S.A.|Department of Mineralogy, E?tv?s L. University, Budapest, H-1117, Pázmány Péter sétány 1/C, Hungary;

    Department of Geology, National Science Museum, 3-23-1 Hyakunincho, Shinjuku, Tokyo 169-0073, Japan;

    Department of Geology, National Science Museum, 3-23-1 Hyakunincho, Shinjuku, Tokyo 169-0073, Japan;

    Department of Geological Sciences, Arizona State University, Tempe, Arizona 85287-1404, U.S.A.|Department of Chemistry/Biochemistry, Arizona State University, Tempe, Arizona 85287-1604, U.S.A.;

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