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首页> 外文期刊>Astronomy and astrophysics >The 10?μm band in amorphous MgSiO3: the influence of medium-range structure, defects and thermal processing
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The 10?μm band in amorphous MgSiO3: the influence of medium-range structure, defects and thermal processing

机译:非晶态MgSiO3中的10?μm谱带:中等范围结构,缺陷和热处理的影响

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Context. Variations in the 10?μm amorphous silicate band profile between different environments have been variously attributed to differences in composition, grain processing or macroscopic constitution (e.g. compact versus aggregate grains). However the relationship with mineralogical structure has remained poorly defined. Aims. The relationship between the 10?μm band and medium-range (~2–20??) structure is investigated. Methods. Synchrotron X-ray scattering, Fourier transform infrared and Raman spectroscopy are used to relate changes in medium-range structure to changes in the 10?μm band profile for amorphous MgSiO3 annealed at temperatures leading up to crystallisation. Results. Raman and X-ray data show a build up of strain within the silicate network, which is released between ~400–550?°C, causing a relaxation of both the Si-O-Si bond angle and Si-O bond length. Decomposing the 10?μm band at each temperature step shows SiO3 is the initially dominant component and increases in proportion as other species become incorporated into the silicate structure. However at ~400?°C the proportion of SiO3 decreases as species with greater numbers of non-bridging oxygens form. The coincidence with strain release implies a breakup of larger tetrahedral structures. Conclusions. We identify a correspondence between the spectral response at 10?μm of amorphous MgSiO3 and the evolution of its structural state at medium-range distances. The dependence of the 10?μm band on medium-range structure may account for the hitherto poor correlation between composition and band behaviour, variations in the 10?μm band observed in other silicates of similar compositions, or, between observed bands in different astronomical settings.
机译:上下文。不同环境之间10?μm非晶态硅酸盐能带分布的变化被不同地归因于组成,晶粒加工或宏观结构(例如压实晶粒与聚集晶粒)的差异。然而,与矿物学结构的关系仍然不清楚。目的研究了10?μm波段与中程(〜2-20?)结构之间的关系。方法。同步加速器X射线散射,傅立叶变换红外光谱和拉曼光谱法用于将中程结构的变化与在导致结晶的温度下退火的非晶MgSiO3的10?μm带谱的变化联系起来。结果。拉曼光谱和X射线数据表明,在约400–550?C之间释放的硅酸盐网络中会累积应变,从而导致Si-O-Si键角和Si-O键长均松弛。在每个温度步骤分解10?μm的谱带,表明SiO3是最初的主要成分,并且随着其他物种掺入硅酸盐结构中而按比例增加。但是,在〜400°C时,SiO 3的比例会随着形成具有更多非桥连氧的物种而减少。应变释放的巧合意味着更大的四面体结构破裂。结论。我们确定了在10μm的非晶态MgSiO3的光谱响应与其在中程距离处的结构状态演变之间的对应关系。 10?μm谱带对中程结构的依赖性可能解释了迄今为止组成和谱带行为之间的相关性较差,在相似组成的其他硅酸盐中观察到的10?μm谱带的变化或在不同天文环境下观察到的谱带之间的差异。 。

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