Dielectric-Relaxation Spectroscopy of Kaolinite, Montmorillonite, Allophane, and Imogolite under Moist Conditions

Tomoyuki Ishida1, Tomoyuki Makino2 and Changjun Wang1
1 Department of Agricultural Engineering, Kagawa University, Miki, Kagawa 761-0795, Japan
2 Soil Chemistry Laboratory, National Institute of Agro-Environmental Sciences of Japan, Tsukuba, Ibaraki 305-8604, Japan
E-mail of corresponding author: ishida@ag.kagawa-u.ac.jp

Abstract: The dielectric behavior of kaolinite, montmorillonite, allophane, and imogolite samples adjusted to a water potential of 33 kPa was examined using a time-domain reflectometry method over a wide frequency range of 103–1010 Hz. A dielectric relaxation peak owing to bound H2O was observed. The observation of this peak required the precise determination of the contributions of dc conductivity. The peak is located at 10 MHz, indicating that the relaxation time of the bound H2O is approximately ten times longer than the relaxation time of bound H2O with organic polymers, such as an aqueous globular-protein solution. The structure of bound H2O differs between phyllosilicates and amorphous phases, based on differences in relaxation strength and the pattern of distribution of the relaxation times. The dielectric process involving rotation of bulk H2O molecules was also observed at 20 GHz. The relaxation strength of bulk H2O increased with an increase in the water content. The interfacial polarization in the diffuse double layer occurred only in montmorillonite and kaolinite, indicating that mechanisms involving the Maxwell-Wagner and surface-polarization effects cannot be extended to include allophane and imogolite. Although these results suggest that additional work is required, a tentative conclusion is that a tangential migration of counter-ions along clay surfaces may be important.

Key Words: Allophane • Bound Water • Complex Permittivity • Dielectric-Relaxation Spectroscopy • Imogolite • Interfacial Polarization • Kaolinite • Montmorillonite • Time-Domain Reflectometry

Clays and Clay Minerals; February 2000 v. 48; no. 1; p. 75-84; DOI: 10.1346/CCMN.2000.0480110
© 2000, The Clay Minerals Society
Clay Minerals Society (www.clays.org)