Induced polarization response of porous media with metallic particles — Part 8: Influence of temperature and salinity

Author:

Revil André1ORCID,Coperey Antoine2ORCID,Mao Deqiang3,Abdulsamad Feras2,Ghorbani Ahmad4ORCID,Rossi Magali5,Gasquet Dominique5

Affiliation:

1. Corresponding author. Université Grenoble Alpes, Université Savoie Mont Blanc, CNRS, IRD, IFSTTAR, ISTerre, 38000 Grenoble, France..

2. Université Grenoble Alpes, Université Savoie Mont Blanc, CNRS, IRD, IFSTTAR, ISTerre, 38000 Grenoble, France..

3. Shandong University, School of Civil Engineering, 17922 Jingshi Road, Jinan 250061, China..

4. Yazd University, Department of Mining and Metallurgical Engineering, Yazd, Iran..

5. Université de Savoie Mont-Blanc, Laboratoire EDYTEM-UMR 5204 du CNRS-Campus Scientifique, F-73376 Le Bourget-du-Lac, France..

Abstract

We have investigated the influence of temperature and salinity upon the spectral induced polarization of 10 samples including rocks with their mineralization (galena, chalcopyrite) plus sand mixed with semiconductors such as magnetite grains, graphite, and pyrite cubes of two different sizes. Measurements are made in a temperature-controlled bath with a high-precision impedance meter and using NaCl solutions. We cover the temperature range 5°C−50°C and the frequency range [Formula: see text] to 45 kHz. For one large pyrite cube, we also investigated six salinities from 0.1 to [Formula: see text] (at 25°C, NaCl) and three salinities for graphite. The spectra are fitted with a Cole-Cole complex parametric conductivity model for which we provide a physical meaning to the four Cole-Cole parameters. As expected, the Cole-Cole exponent and the chargeability are independent of the temperature and salinity. The instantaneous and steady state (direct current [DC]) conductivities depend on the salinity and temperature. This temperature dependence can be fitted with an Arrhenius law (combining the Stokes-Einstein and Vogel-Fulcher-Tammann equations) with an activation energy in the range of [Formula: see text]. This activation energy is the same as for the bulk pore-water conductivity demonstrating the control by the background electrolyte of these quantities, as expected. The instantaneous and DC conductivities depend on the salinity in a predictable way. The Cole-Cole relaxation time decreases with the temperature and decreases with the salinity. This behavior can be modeled with an Arrhenius law with an apparent activation energy of [Formula: see text]. A finite-element model is used further to analyze the mechanisms of polarization, and it can reproduce the temperature and salinity dependencies observed in the laboratory.

Publisher

Society of Exploration Geophysicists

Subject

Geochemistry and Petrology,Geophysics

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