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层状双氢氧化物体系中的插层化学:通过时间分辨原位 X 射线衍射研究阴离子交换过程和阶段现象。

Intercalation chemistry in a LDH system: anion exchange process and staging phenomenon investigated by means of time-resolved, in situ X-ray diffraction.

机构信息

CNRS, UMR 6002, LMI, F-63177 Aubiere-Clermont Université, Laboratoire des Matériaux Inorganiques, BP 10448, F-63000, Clermont-Ferrand.

出版信息

Dalton Trans. 2010 Jul 14;39(26):5994-6005. doi: 10.1039/c001678k. Epub 2010 May 20.

Abstract

Using time-resolved, in situ energy-dispersive X-ray diffraction (EDXRD), the formation of interstratified LDH structures, with alternate interlayer spaces occupied by different anions, have been demonstrated during anion exchange reactions. Novel hybrid LDH nanostructures can thus be prepared, combining the physicochemical properties of two intercalated anions plus those of the LDH host. A general trend is that inorganic-inorganic anion exchange reactions occur in a one-step process while inorganic-organic exchanges may proceed via a second-stage intermediate, suggesting that staging occurs partly as a result of organic-inorganic separation. Yet, other influencing parameters must be considered such as LDH host composition, LDH affinity for different anions and LDH particle size as well as extrinsic parameters like the reaction temperature. Hence, a correlation between the occurrence of staging phenomenon and the difficulty of the exchange of the initial anion is observed, suggesting that staging is needed to overcome the energy barrier in the case of the exchange by organic anions. Notwithstanding the LiAl(2) system, staging has mainly been observed with Zn(2)Cr LDH host so far, a peculiar LDH composition with a unique Zn/Cr ratio of two and a local order of the cations within the hydroxide layers. The formation of a higher order-staged intermediate than stage two, observed during the exchange reaction of CO(3)(2-) or SO(4)(2-) anions with Zn(2)Cr-tartrate, is in favour of a Daumas-Herold model although this model implies a bending of LDH layers. The analysis of the X-ray powder diffraction pattern of Zn(2)Cr-Cl/tartrate second-stage intermediate, isolated almost as a pure phase during the exchange of Cl(-) with tartrate anions in Zn(2)Cr LDH, indicates a disorder in the stacking sequence and a relative proportion of the two kinds of interlayers slightly different from 50/50. Besides, the microstructural analysis of the XRD pattern reveals a great reduction of the stacking thickness during the anion exchange process but with no change of the in-plane coherent length, therefore no in-plane deformation of LDH host layers. Finally, the anion exchange properties of Zn(2)Cr-Cl/tartrate, investigated by means of EDXRD, show highly selective anion-exchange reactions, leading to the formation of new second-stage intermediates that cannot be prepared starting from the mono-intercalated Zn(2)Cr-Cl. This "Zn(2)Cr-Cl/tartrate approach" might constitute a new route for the synthesis of various mixed organic-inorganic anions-exchanged forms of LDH.

摘要

利用时间分辨、原位能量色散 X 射线衍射(EDXRD),在阴离子交换反应过程中,已经证明了具有交替层间空间的层状双氢氧化物(LDH)结构的形成,其中不同的阴离子占据交替层间空间。因此,可以制备新型的混合 LDH 纳米结构,将两种插层阴离子的物理化学性质与 LDH 主体的性质结合在一起。一般来说,无机-无机阴离子交换反应是一步进行的,而无机-有机交换可能通过第二阶段中间体进行,这表明分级反应部分是由于有机-无机分离造成的。然而,还必须考虑其他影响参数,如 LDH 主体组成、LDH 对不同阴离子的亲和力以及 LDH 颗粒大小,以及反应温度等外在参数。因此,观察到分级现象的发生与初始阴离子交换的难度之间存在相关性,这表明在交换有机阴离子时需要分级来克服能量障碍。尽管 LiAl(2) 体系是一个例外,但到目前为止,主要在 Zn(2)Cr LDH 主体中观察到分级现象,这是一种具有独特 Zn/Cr 比为 2 和氢氧化物层内阳离子局部有序的特殊 LDH 组成。在 CO(3)(2-)或 SO(4)(2-)阴离子与 Zn(2)Cr-酒石酸交换反应过程中观察到的高于第二阶段的更高阶分级中间相的形成有利于 Daumas-Herold 模型,尽管该模型意味着 LDH 层的弯曲。对 Zn(2)Cr-Cl/酒石酸第二阶段中间相的 X 射线粉末衍射图谱的分析表明,在 Zn(2)Cr LDH 中用酒石酸阴离子交换 Cl(-)时,几乎以纯相形式分离出来的 Cl(-)/酒石酸交换反应中,堆积序列存在无序,两种层间的相对比例略低于 50/50。此外,XRD 图谱的微观结构分析表明,在阴离子交换过程中堆积厚度大大减小,但面内相干长度没有变化,因此 LDH 主体层没有面内变形。最后,通过 EDXRD 研究了 Zn(2)Cr-Cl/酒石酸的阴离子交换性能,结果表明该化合物具有高度选择性的阴离子交换反应,导致形成了不能由单插层 Zn(2)Cr-Cl 起始制备的新型第二阶段中间相。这种“Zn(2)Cr-Cl/酒石酸方法”可能为合成各种混合有机-无机阴离子交换形式的 LDH 提供了一种新途径。

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