Abstract

AbstractNuclear magnetic resonance (NMR) provides a powerful tool to describe local nuclear environments. In this work, unique structural information on kaolinite and on kaolinite dimethylsulfoxide (DMSO) intercalate were provided by solid-state 1H and 27Al magic-angle spinning (MAS) NMR. The interlayer chemistry of kaolinite (K) was examined by intercalating a select group of highly polar organic molecules or salts into kaolinite as a first step. Once the interlayer space is expanded, the intercalated compounds can be replaced in a second step. Intercalating DMSO into kaolinite to form the DMSO-K intercalate is, thus, a particularly useful first step toward the intercalation of a large variety of molecules, including polymers and ionic liquids. Well developed characterization methods are essential to define the structural modifications of kaolinite, and MAS NMR is a useful complement to other techniques. The use of 1H and 27Al MAS NMR for this purpose has been relatively rare. 1H NMR, nevertheless, can give unique information about kaolinite hydroxyls. Because quadrupolar interactions are sensitive to the local octahedral Al(III) geometry, solid-state 27Al NMR can follow subtle structural modifications in the octahedral sheet. In the present work, the 1H MAS NMR chemical shifts of KGa-1b were unambiguously attributed to the internal surface hydroxyls at 2.7 ppm and to the internal hydroxyls at 1.7 ppm. The 1H MAS NMR chemical shifts of the two methyl groups in DMSO-K are not equivalent and can be attributed to the 2.9 and 4.2 ppm peaks. The 27Al MAS NMR spectra of KGa-1b obtained under different magnetic fields revealed that most of the quadrupolar effects were highly reduced at 21.1 T, whereas the spectra at lower field, 4.7 T, were dominated by quadrupolar effects. The two octahedral Al(III) sites are not equivalent and can be distinguished in the low-field spectral simulation. Increased quadrupolar constants were observed and showed the major perturbations of the local Al symmetry that resulted from DMSO intercalation. Both the 1H and 27Al MAS NMR studies at different magnetic fields afforded important information about the local environments of the kaolinite hydroxyl groups and structural Al(III).

Highlights

  • Clay minerals are known for many unique chemical and physical properties that make them attractive starting materials for a vast variety of applications (Johnston, 2010; Bergaya and Lagaly, 2013)

  • Kaolinite was partially deuterated by exchanging the hydroxyl protons in a Figure 9. 27Al 3QMAS Nuclear magnetic resonance (NMR) spectra of (a) KGa-1b and (b) Dimethyl sulfoxide - kaolinite intercalate (DMSO-K) obtained at 21.1 T using a magic-angle spinning (MAS) rate of 18 kHz

  • Two signals with a 3:1 ratio were attributed to the kaolinite hydroxyls and two signals were attributed to the two non-equivalent DMSO methyl groups with identical intensities at 2.9 and 4.2 ppm

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Summary

Introduction

Clay minerals are known for many unique chemical and physical properties that make them attractive starting materials for a vast variety of applications (Johnston, 2010; Bergaya and Lagaly, 2013). When the temperature was increased above 320 K, some of the DMSO methyl groups were released from the ditrigonal cavities (Hayashi, 1997) and the interlayer DMSO that remained was H-bonded through the DMSO sulfonyl group to the aluminol groups. This behavior made DMSOK a useful and efficient starting material for the intercalation of a large variety of small molecules, polymers, and ionic liquids into kaolinite (Letaief et al, 2008; Tonle et al, 2009; Dedzo and Detellier, 2016). An in-depth evaluation of the methods to intercalate DMSO into kaolinite was recently published (Abou-El-Sherbini et al, 2017)

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