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Clays and Clay Minerals; June 2004; v. 52; no. 3; p. 350-356; DOI: 10.1346/CCMN.2004.0520310
© 2004 Clay Minerals Society
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CONFORMATION OF SURFACTANT MOLECULES IN THE INTERLAYER OF MONTMORILLONITE STUDIED BY 13C MAS NMR

Hongping He1,2,3,*, Ray L. Frost2, Feng Deng3, Jianxi Zhu1,3, Xiaoyan Wen3 and Peng Yuan1,3

1 Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Wushan, Guangzhou 510640, China
2 Inorganic Materials Research Program, School of Physical and Chemical Sciences, Queensland University of Technology, GPO Box 2434, Brisbane, QLD 4001, Australia
3 National Laboratory of Magnetic Resonance and Atom and Molecular Physics, Wuhan Institute of Physics, Chinese Academy of Sciences, Wuhan 430071, China

* E-mail address of corresponding author: hehp{at}gig.ac.cn

The ordering conformation of surfactant molecules in intercalated montmorillonite prepared at various concentrations was investigated by 13C MAS NMR. The 13C MAS NMR study demonstrates the coexistence of ordered and disordered chain conformations. Two main resonance peaks are associated with the backbone alkyl chains: the resonance at 33 ppm corresponds to the ordered conformation (all-trans), and the resonance at 30 ppm corresponds to the disordered conformation (mixture of trans and gauche). Deconvolution of 13C MAS NMR spectra indicates that the ordering conformation of surfactant molecules within the gallery of montmorillonite depends very much on their orientation and packing density. When amine chains are oriented parallel to the silicate layers, the amount of all-trans conformer decreases with the increase of amine concentration. However, the amount of all-trans conformer increases with the increase of amine concentration when amine chains radiate from the silicate layers. Furthermore, 13C MAS NMR spectra show that the intercalated surfactant molecules in the clay minerals never attained the complete liquidlike or solidlike behavior.

Key Words: 13C MAS NMR • Conformation • Montmorillonite • Surfactant




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