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首页> 外文期刊>Journal of the American Chemical Society >Topologically Ordered Amorphous Silica Obtained from the Collapsed Siliceous Zeolite, Silicalite-1-F: A Step toward 'Perfect' Glasses
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Topologically Ordered Amorphous Silica Obtained from the Collapsed Siliceous Zeolite, Silicalite-1-F: A Step toward 'Perfect' Glasses

机译:从坍塌的硅质沸石Silicalite-1-F中获得的拓扑有序无定形二氧化硅:迈向“完美”玻璃的一步

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摘要

A dense amorphous form of silica was prepared at high pressure from the highly compressible, siliceous zeolite, silicalite-1 -F. Reverse Monte Carlo modeling of total X-ray scattering data shows that the structure of this novel amorphous form of SiO_2 recovered under ambient conditions is distinct from vitreous SiO_2 and retains the basic framework topology (i.e., chemical bonds) of the starting crystalline zeolite. This material is, however, amorphous over the different length scales probed by Raman and X-ray scattering due to strong geometrical distortions. This is thus an example of new topologically ordered, amorphous material with a different intermediate-range structure, a lower entropy with respect to a standard glass, and distinct physical and mechanical properties, eventually approaching those of an "ordered" or "perfect" glass. The same process in more complex aluminosilicate zeolites will, in addition, lead to an amorphous material which conserves the framework topology and chemical order of the crystal. The large volume collapse in this material may also be of considerable interest for new applications in shock wave absorption.
机译:在高压下,由高度可压缩的硅质沸石silicalite-1-F制备致密的非晶形二氧化硅。反向X射线总X射线散射数据的蒙特卡洛模型表明,这种在环境条件下回收的新型SiO_2非晶态结构与玻璃态SiO_2不同,并保留了起始结晶沸石的基本骨架拓扑结构(即化学键)。但是,由于强烈的几何变形,这种材料在拉曼和X射线散射探测的不同长度尺度上都是非晶态的。因此,这是一种新的拓扑有序的无定形材料的示例,该材料具有不同的中间范围结构,相对于标准玻璃具有较低的熵以及独特的物理和机械性质,最终接近“有序”或“完美”玻璃的性质。另外,在更复杂的铝硅酸盐沸石中的相同过程将导致形成非晶态材料,该非晶态材料保留了晶体的骨架拓扑和化学顺序。对于冲击波吸收的新应用,这种材料中的大量塌陷也可能引起相当大的兴趣。

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  • 来源
    《Journal of the American Chemical Society》 |2009年第34期|12333-12338|共6页
  • 作者单位

    Institut Charles Gerhardt Montpellier, Equipe PMOF, UMR 5253 CNRS-UM2-ENSCM-UM1, Universite Montpellier II, Sciences et Techniques du Languedoc, Place E. Bataillon cc1504, 34095 Montpellier Cedex 05, France;

    Laboratoire des Colloiedes, Verres et Nanomateriaux, UMR 5587 CNRS UM2, Universite Montpellier II, Place Eugene Bataillon, 34095 Montpellier Cedex 5, France;

    CEA, DAM Le Ripault, F-37260 Monts, France;

    CEA, DAM Le Ripault, F-37260 Monts, France;

    Research & Utilization Division, Japan Synchrotron Radiation Research Institute (JASRI, SPring-8) 1-1-1 Kouto, Sayo-cho, Sayo-gun, Hyogo 679-5198, Japan;

    ISIS Facility, Rutherford Appleton Laboratory, HSIC, Didcot, Oxfordshire, OX11 0QX, United Kingdom Department of Physics, Oxford University, Clarendon Laboratory, Parks Road, Oxford, OX1 3PU, United Kingdom;

    Laboratoire Magmas et Volcans, UMR CNRS 6524, Universite Blaise Pascal, 63038 Clermont-Ferrand Cedex, France;

    Laboratoire Magmas et Volcans, UMR CNRS 6524, Universite Blaise Pascal, 63038 Clermont-Ferrand Cedex, France;

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