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Hydration performance of dioctahedral smectite saturated with Ba2+ and Cs+ cations: Quantitative XRD investigation

机译:用Ba 2 + 2 + 和Cs + 阳离子饱和Dioctahedral蒙脱石的水合性能:定量XRD调查

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The present paper aims at characterizing the hydration behavior in the case of dioctahedral smectite with different location charge (i.e. montmorillonite SWy-2 and beidellite SbId-1) exchanged by heavy metals ca < “(tions characterized by different valence (Ba2+ and Cs+) generally coming from industrial waste and wastewater solution. The study was performed basing on the quantitative X-ray diffraction investigation. This method consists on the comparison between experimental patterns with a theoretical ones calculated from structural models and allows us to determine the relative proportions of different hydration states (dehydrated.0W, monohydrated.1W, or bihydrated.2W,) that can coexist within smectite structure. Furthermore, position and amount of both interlayer water molecules and heavy metals cations can be also, determined along the c* axis. Obtained qualitative and quantitative XRD analysis showed the possibility to distinguish diverse hydration behavior of each complex. The presence of the monovalent cation (i.e. Cs+) in the interlayer space of both smectite restricts the water molecule intercalation that structures are dominated by two principal hydration states: 1 W and 0W. Whereas in the case of the bivalent cation (i.e. Ba2+), the interlayer water amount retuned in the beidellite and montmorillonite structure is more important seen the presence of a major bihydrated layers types in their interlayer's spaces.
机译:本文旨在表征在用重金属Ca <“(以不同价值特征的蒙脱石Swy-2和Beidellite SBID-1)的不同位置电荷(即蒙脱石Swy-2和Beidellite SBID-1)的情况下进行水化行为。(Ba 2通常来自工业废物和废水溶液的+ / sup>和cs + 。该研究基于定量X射线衍射调查。该方法包括实验模式与a的比较从结构模型计算的理论上,并且我们允许我们确定可以在蒙脱石结构中共存的不同水合态(脱水,一元水合的0w或Bi)的相对比例。此外,层间水分子的位置和量和重金属阳离子也可以沿着C *轴线确定。获得的定性和定量XRD分析显示有可能区分多样化的水合行为o f每个复杂的。两种蒙脱石的中间间空间中的单价阳离子(即cs + )的存在限制了水分子插入,即结构由两个主要水合态主要为:1w和0w。而在二价阳离子的情况下(即Ba 2 + ),在北角和蒙脱石结构中重新调整的层间水量更重要,看得其在其中间层的空间中存在主要的Bydrate层类型。

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