Synthesis, crystal structure and temperature-dependent properties of gallogermanate nitrite sodalite [Na8(NO2)2][GaGeO4]6

被引：8

作者：

Poltz, Irma ^{[1
,2
]}

Robben, Lars ^{[1
]}

Buhl, Josef-Christian ^{[2
]}

Gesing, Thorsten M. ^{[1
]}

机构：

[1] Univ Bremen, D-28359 Bremen, Germany

[2] Leibniz Univ Hannover, Inst Mineral, D-30167 Hannover, Germany

来源：

MICROPOROUS AND MESOPOROUS MATERIALS | 2015年 / 203卷

关键词：

Inorganic compounds; Microporous materials; X-ray diffraction; Crystal structure; Thermal expansion; THERMAL-EXPANSION BEHAVIOR; HYDROTHERMAL SYNTHESIS; PHASE-TRANSITIONS; GALLIUM; ANION; FRAMEWORKS; SPECTRA; FAMILY; CATION; RAMAN;

D O I：

10.1016/j.micromeso.2014.10.007

中图分类号：

O69 [应用化学];

学科分类号：

081704 ;

摘要：

[Nas(NO2)(2)][GaGeO4](6) sodalite was synthesized in a two-step process, starting with the formation of gallogermanate basic-hydro-sodalite under mild hydrothermal conditions (1) followed by hydrothermal treatment in concentrated NaNO2 solution (2). The presence of NO in the sodalite framework was verified by FTIR and Raman spectroscopy. Crystal structure refinements were performed in the space group P (4) over bar 3n from X-ray powder diffraction data using the Rietveld method. a = 915.28(1) pm, V = 766.8(1) x 10(-6) pm(3), R-B = 1.92%. The nitrogen atoms were refined on the 8e (x, x, x) crystallographic position with 1/4 occupancy. Temperature-dependent properties were investigated by TG-DTA and in-situ X-ray powder diffraction. Debye-Anharmonicity model fit evaluation of the thermal expansion coefficient and the temperature-dependent cell volume behavior indicate intra-cage nitrite to nitrate oxidation around 850 K, confirmed by ex-situ FTIR spectroscopy. The sodalite framework decomposition follows around 935 K, resulting in the beryllonite-type NaGaGeO4. (C) 2014 Elsevier Inc. All rights reserved.

引用

页码：100 / 105

页数：6

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