1976
DOI: 10.2118/5505-pa
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The Determination of Qv From Membrane Potential Measurements on Shaly Sands

Abstract: This technique determines the value of cation-exchange capacity per unit pore volume (QJ of a shaly sand formation sample by using it as a membrane in an electrochemical cell. This new technique is nondestructive, eliminates prior core analyses, uses small samples, and provides representative values of Q, for nonisotropic and homogeneous samples. JOURNAL OF PETROLEUM TECHNOLOGY

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Cited by 56 publications
(29 citation statements)
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“…1). The cation exchange capacity (CEC), which is the quantity of exchangeable cations on a negatively charged mineral surface, is not the same for these two clay minerals: For smectite the CEC is 0.8-1.5 meq/g (Ellis, 1987); for chlorite, 0.01 meq/g (Thomas, 1976). This could explain the difference in conductivity between the smectite/zeolite and the chlorite/epidote alteration zones.…”
Section: Electrical Conduction Mechanisms and Their Temperature Depenmentioning
confidence: 99%
“…1). The cation exchange capacity (CEC), which is the quantity of exchangeable cations on a negatively charged mineral surface, is not the same for these two clay minerals: For smectite the CEC is 0.8-1.5 meq/g (Ellis, 1987); for chlorite, 0.01 meq/g (Thomas, 1976). This could explain the difference in conductivity between the smectite/zeolite and the chlorite/epidote alteration zones.…”
Section: Electrical Conduction Mechanisms and Their Temperature Depenmentioning
confidence: 99%
“…However, interpretation is complicated by the presence of clay minerals. Clays consist essentially of alumino-silicate minerals, which have a deficit of charge due to (1) substitution of ions in the crystal structure by ions of different valence, and (2) acid/base reactions between surface silanol/aluminol groups and water [e.g., Thomas, 1976]. The "counterions" required to counterbalance this charge deficit are located in the so-called electrical double layer [Waxman and Srnits, 1968;Avena and De Pauli, 1996; and Janusz et al, 1997].…”
Section: Introductionmentioning
confidence: 99%
“…The Hanai-Bruggeman equation [Bruggeman, 1935;Hanai, 1960Hanai, , 1961BussJan, 1983] was developed using a self- (Table 1). For NaC1, 0.38, and for KC1, t(•+) (K +) --0.50 [e.g., Thomas, 1976]. To first approximation, the Hittorf transport numbers in the free electrolyte are independent of both salinity and temperature s and t•_) as [e.g., Thomas, 1976].…”
Section: Introductionmentioning
confidence: 99%
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“…) is the mobility of the counterions responsible for surface electrical conduction in the vicinity of the pore water/mineral interface, b S (Na + , 25°C) = 0.51 Â 10 À8 m 2 s À1 V À1 [Revil et al, 1998], s S corresponds to surface conductivity, and t (+) is the fraction of electrical current carried in the free electrolyte by the cations, t (+) (Na + ) % 0.38 independent of both salinity and temperature [Thomas, 1976]. The cation exchange capacity of the clay fraction, CEC Sh , can be related to the cation exchange capacity of the whole sediment, CEC, and to the cation exchange capacity of each clay component (in the present case CEC(C) for chlorite and CEC(I) for illite, both being fairly well-constrained parameters, see Table 1) by…”
Section: Influence Of Salinity and Clay Contentmentioning
confidence: 99%