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Journal ArticleDOI

Infrared and Raman study of interlayer anions CO32–, NO3–, SO42– and ClO4– in Mg/Al-hydrotalcite

TLDR
In this article, the difference in the local environment of CO32−, NO3−, SO42−, and ClO4− in Mg/Al-hydrotalcite compared to the free anions was studied by infrared and Raman spectroscopy.
Abstract
The difference in the local environment of CO32−, NO3−, SO42−, and ClO4− in Mg/Al-hydrotalcite compared to the free anions was studied by infrared and Raman spectroscopy. In comparison to free CO32− a shift toward lower wavenumbers was observed. A band around 3000–3200 cm−1 has been attributed to the bridging mode H2O-CO32−. The IR spectrum of CO3− hydrotalcite clearly shows the split ν3 band around 1365 and 1400 cm−1 together with weak ν2 and ν4 modes around 870 and 667 cm−1. The ν1 mode is activated and observed as a weak band around 1012 cm−1. The Raman spectrum shows a strong ν1 band at 1053 cm−1 plus weak ν3 and ν4 modes around 1403 and 695 cm−1. The symmetry of the carbonate anions is lowered from D 3 h to C 2 s resulting in activation of the IR inactive ν1 mode around 1050–1060 cm−1. In addition, the ν3 shows a splitting of 30–60 cm−1. Although NO3-hydrotalcite has incorporated some CO32− the IR shows a strong ν3 mode at 1360 cm−1 with a weak band at 827 cm−1, and the ν4 band is observed at 667 cm−1, although it is largely obscured by the hydrotalcite lattice modes. The Raman spectrum shows a strong ν1 mode at 1044 cm−1 with a weaker ν4 band at 712 cm−1. The ν3 mode at 1355 cm−1 is obscured by a broad band due to the presence of CO32−. The symmetry of NO3− did not change when incorporated in hydrotalcite. The IR spectrum of SO4-hydrotalcite shows a strong ν3 at 1126, ν4 at 614 and a weak ν1 mode at 981 cm−1. The Raman spectrum is characterized by a strong ν1 mode at 982 cm−1 plus medium ν2 and ν4 bands at 453 and 611 cm−1; ν3 cannot be identified as a separate band, although a broad band can be seen around 1134 cm−1. The site symmetry of SO42− is lowered from T d to C 2 v . The distortion of ClO4− in the interlayer of hydrotalcite is reflected in the IR spectrum with both ν3 and ν4 bands split around 1096 and 1145 cm−1 and 626 and 635 cm−1, respectively. A weak ν1 band is observed at 935 cm−1. The Raman spectrum shows a strong ν1 mode at 936 cm−1 plus ν2 and ν4 bands at 461 and 626 cm−1, respectively. A ν3 mode cannot be clearly recognized, but a broad band is visible around 1110 cm−1. These data indicative a lowering of symmetry from T d to C s .

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Structural aspects of layered double hydroxides

TL;DR: A review of experimental and theoretical studies of the structure of LDHs can be found in this article, highlighting areas of consensus and currently unresolved issues, including the range of composition for which LDH may be formed, possible layer stacking polytypes, arrangement of guest species in the interlayer galleries and the extent of order-disorder phenomena, both long-range and short-range, in the layers and inter-layer galleries.
Journal ArticleDOI

In Situ Transformation of MOFs into Layered Double Hydroxide Embedded Metal Sulfides for Improved Electrocatalytic and Supercapacitive Performance

TL;DR: This study demonstrates self-templated pseudomorphic transformation of MOF into surface chemistry rich hollow framework that delivers highly reactive, durable, and universal electrochemically active energy conversion and storage functionalities.
Journal ArticleDOI

Intercalation of Mg–Al layered double hydroxide by anionic surfactants: Preparation and characterization

TL;DR: In this paper, the preparation and characterization of intercalation compounds of Mg-Al layered double hydroxide (Mg−Al LDH) and various organic surfactants have been studied in detail.
Journal ArticleDOI

FT‐Raman and FT‐IR spectroscopic study of synthetic Mg/Zn/Al‐hydrotalcites

TL;DR: In this paper, the FT-Raman and FT-IR spectroscopy was used to characterize synthetic Mg/Zn/Al-hydrotalcites with atomic ratios of 6:0:2, 4:2 :2, 2:4:2 and 0:6:2.
Journal ArticleDOI

Deintercalation of Carbonate Ions from a Hydrotalcite-Like Compound: Enhanced Decarbonation Using Acid−Salt Mixed Solution

TL;DR: In this article, the authors found that the addition of NaCl dramatically enhanced the deintercalation of carbonate ions by dilute HCl solution (0.0025−0.005 N).
References
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Book

Infrared and Raman Spectra of Inorganic and Coordination Compounds

TL;DR: In this article, the normal modes of vibration are illustrated and corresponding vibrational frequencies are listed for each type, including diatomic, triatomic, fouratomic, five-atomic, six-atomic and seven-atomic types.
Book

The Infrared spectra of minerals

V. C. Farmer
TL;DR: The use of vibrational spectroscopy as a tool in identifying mineral species and in deriving information concerning the structure, composition and reactions of minerals and mineral products is discussed in this paper.
Journal ArticleDOI

The Syntheses of Hydrotalcite-Like Compounds and Their Structures and Physico-Chemical Properties I: The Systems Mg2+-Al3+-NO3-, Mg2+-Al3+-Cl-, Mg2+-Al3+-ClO4-, Ni2+-Al3+-Cl- and Zn2+-Al3+-Cl-

TL;DR: The basic salts of this system were prepared and their structures and physico-chemical properties were studies by electron microscopy, chemical analysis, X-ray powder diffraction, thermal analysis, and acidity-basicity measurements as mentioned in this paper.
Journal ArticleDOI

Preparation and catalytic properties of cationic and anionic clays

Angelo Vaccari
- 28 May 1998 - 
TL;DR: In this paper, the structure, main properties and preparation methods of cationic and anionic clays are reviewed in light of the versatility and potential of these materials, which may be useful tools in the move towards establishing environmentally friendly technologies.
Journal ArticleDOI

The nature of the thermal decomposition of a catalytically active anionic clay mineral

TL;DR: In this article, the changes which take place during heat activation of hydrotalcite have been studied by 27Al nuclear magnetic resonance-magic angle spinning, Auger and XPS spectroscopy, transmission electron microscopy, and high resolution nitrogen desorption techniques.
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