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FT-Raman and power XRD analysis of the Ba(SO_4)_x(CrO_4)_(1-x) solid solution

机译:Ba(SO_4)_x(CrO_4)_(1-x)固溶体的FT-拉曼光谱和功率XRD分析

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摘要

The Ba(SO_4)_x(CrO_4)_(1-x) solid solution has been described in nature, forming the mineral Hashemite. From the geochemical point of view, however, anionic solid solutions have much interest because they are suitable systems to probe order-disorder phenomena. The solid solution analysed in the present study has, moreover, a special incentive in its possible use for the extraction from water, and immobilisation, of the pollutant Cr(VI)ion. The orthorhombic (space group Pnma) unit cell parameters of the solid solution change linearly with the mole fraction of both anions, decreasing with increase in the sulfate anion concentration. The vibrational spectroscopic study is centred on the behaviour of the anionic symmetric stretching band (v_1,A_1), whose characteristics are examined in detail. While the chromate anion band retains its wavenumber along the full compositional range, the sulfate anion band is shifted toward lower wavenumbers with decrease in the corresponding mole fraction. The positional disorder induced by the random anionic substitution results in strong increase of the halfwidth in both bands, which becomes greatest in the central member of the series.
机译:在自然界中已经描述了Ba(SO_4)_x(CrO_4)_(1-x)固溶体,形成了矿物杂波石。但是,从地球化学的观点来看,阴离子固溶体引起了极大的兴趣,因为它们是探测有序现象的合适系统。此外,本研究中分析的固溶体在其可能用于从水中提取和固定化污染物Cr(VI)离子方面具有特殊的诱因。固溶体的斜方晶(空间群Pnma)晶胞参数随两种阴离子的摩尔分数线性变化,随硫酸根阴离子浓度的增加而减小。振动光谱研究的重点是阴离子对称拉伸带(v_1,A_1)的行为,详细研究了其特性。铬酸盐阴离子带在整个组成范围内保持波数不变,而硫酸根阴离子带随着相应摩尔分数的降低而向较低波数移动。由无规阴离子取代引起的位置紊乱导致两个谱带的半峰宽度大大增加,这在系列的中心部分变得最大。

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