Costantino Umberto, Vivani Riccardo, Bastianini Maria, Costantino Ferdinando, Nocchetti Morena
Dipartimento di Chimica, Biologia e Biotecnologie, Università di Perugia, Via Elce di Sotto, 8, Perugia, 06123, Italy.
Dalton Trans. 2014 Aug 14;43(30):11587-96. doi: 10.1039/c4dt00620h. Epub 2014 Jun 18.
A layered double hydroxide (LDH) obtained by the urea method, having an empirical formula Zn(0.61)Al(0.39)(OH)2(0.195)·0.50H2O, has been converted into the corresponding chloride form [Zn(0.61)Al(0.39)(OH)2]Cl(0.39)·0.47H2O by making the solid come into contact with a suitable HCl solution. The intercalation of the other halide anions (X(-) = F(-), Br(-), I(-)) via the Cl(-)/X(-) anion exchange has been attained and the respective anion exchange isotherms have been obtained with the batch method. The analysis of the isotherms indicates that the selectivity of LDH towards the halides decreases with the increase of the X(-) ionic radius, the selectivity order being F(-) > Cl(-)≥ Br(-) > I(-). The CO3(2-)/Cl(-) isotherm has also been reported to highlight the extraordinary selectivity of LDH towards carbonate anions. Samples taken from the isotherms at different exchange degrees were analyzed by X-ray diffraction, thermogravimetry and thermodiffractometry to obtain information about the ion exchange mechanism. The Cl(-)/Br(-) and the reverse Br(-)/Cl(-) exchanges occur with the formation of solid solutions, very likely because of the similar ionic radius of the exchanging anions. In contrast, in the Cl(-)/F(-) and Cl(-)/I(-) exchange, the co-existence of the Cl(-) and F(-) (or I(-)) phases in the same sample was detected, indicating the occurrence of a first order phase transition, in which the starting phase is transformed into the final phase, as the process goes on. The variation of the interlayer distances of ZnAl-X intercalation compounds with the hydration degree has been interpreted with a structural model based on the nesting of the guest species into the trigonal pockets of the brucite-like layer surface. Rietveld refinements of the phases with the maximum F(-), Br(-) and I(-) content were also performed and compared with the above model, giving indications of the arrangement and order/disorder of the halide anions in the interlayer region.
通过尿素法获得的层状双氢氧化物(LDH),其经验式为Zn(0.61)Al(0.39)(OH)2(0.195)·0.50H2O,通过使该固体与合适的HCl溶液接触,已转化为相应的氯化物形式[Zn(0.61)Al(0.39)(OH)2]Cl(0.39)·0.47H2O。通过Cl(-)/X(-)阴离子交换实现了其他卤化物阴离子(X(-)=F(-)、Br(-)、I(-))的插层,并采用分批法获得了相应的阴离子交换等温线。对等温线的分析表明,LDH对卤化物的选择性随X(-)离子半径的增加而降低,选择性顺序为F(-)>Cl(-)≥Br(-)>I(-)。还报道了CO3(2-)/Cl(-)等温线,以突出LDH对碳酸根阴离子的非凡选择性。通过X射线衍射、热重分析和热衍射对不同交换程度的等温线样品进行分析,以获取有关离子交换机制的信息。Cl(-)/Br(-)和反向Br(-)/Cl(-)交换伴随着固溶体的形成而发生,这很可能是由于交换阴离子的离子半径相似。相比之下,在Cl(-)/F(-)和Cl(-)/I(-)交换中,检测到同一样品中Cl(-)和F(-)(或I(-))相共存,表明发生了一级相变,随着过程的进行,起始相转变为最终相。基于客体物种嵌套在类水镁石层表面的三角口袋中,用结构模型解释了ZnAl-X插层化合物层间距离随水合程度的变化。还对F(-)、Br(-)和I(-)含量最高的相进行了Rietveld精修,并与上述模型进行了比较,给出了卤化物阴离子在层间区域的排列和有序/无序情况。