Determination of ion association in dilute aqueous lithium chloride and lithium hydroxide solutions to 600°C and 300 MPa by electrical conductance measurements

被引:40
作者
Ho, PC [1 ]
Palmer, DA [1 ]
机构
[1] Oak Ridge Natl Lab, Div Chem & Analyt Sci, Oak Ridge, TN 37831 USA
关键词
D O I
10.1021/je970198b
中图分类号
O414.1 [热力学];
学科分类号
摘要
The limiting molar conductances (Lambda(0)) and ion association constants of dilute aqueous lithium chloride and lithium hydroxide solutions (<0.01 mol.kg(-1)) were determined by electrical conductance measurements at temperatures from 100 to 600 degrees C and pressures up to 300 MPa. The values of Lambda(0)(LiCl) and Lambda(0)(LiOH) obtained from with Shedlovsky (at densities greater than or equal to 0.6 g.cm(-3)) and Fuoss-Hsia-Fernandez-Prini (FHFP) equations (at densities <0.6 g.cm(-8)) increase with increasing temperature up to 300 degrees C and decreasing density. Above 300 degrees C and densities between 0.8 and 0.5 g.cm(-3) for LiCl(aq) and 0.8 to 0.6 g.cm(-3) for LiOH(aq), Lambda(0) is nearly temperature-independent but does increase linearly with decreasing density. The molal association constants, K-A(m) for both electrolytes were computed exclusively from the data greater than or equal to 400 degrees C (at densities 0.8-0.3 for LiCl and 0.8-0.5 g.cm(-3) for LiOH) by the Shedlovsky equation and can be represented as functions of temperature (Kelvin) and the logarithm of water density (rho(w)) as follows: log K-A(m)(LiCl) = 0.724 - 8.980/(T/X) - (12.796 - 5431.2/(T/K)) log rho(w)/g.cm(-3)) and log K-A(m)(LiOH) = 0.856 + 135.60/(T/K) - (11.998 - 4226.3/(T/K)) log rho(w)/(g.cm(-3)). At corresponding conditions and within experimental error, the degree of ion association of LiCl(aq) is comparable with NaCl(aq) and KCl(aq), whereas ion association for LiOH(aq), is significantly stronger than for NaOH(aq) and KOH(aq). Moreover, the same values of K-A(m) were obtained for each electrolyte irrespective of the whether the Shedlovsky or FHFP equations were employed. This point is exemplified by a comparison of the K-A(m) value for LiCl obtained from the present study with those of a recent investigation that utilized an advanced design for moderately high temperature conductance measurements.
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页码:162 / 170
页数:9
相关论文
共 28 条
[1]  
[Anonymous], 1983, COMPREHENSIVE TREATI
[2]  
[Anonymous], WATER COMPREHENSIVE, DOI [10.1007/978-1-4684-8334-5_13, DOI 10.1007/978-1-4684-8334-5_13]
[3]   VOLUMETRIC PROPERTIES OF AQUEOUS-ELECTROLYTES AT HIGH-TEMPERATURE - MIXTURES OF LIOH AND KOH UP TO 523-K [J].
CORTI, HR ;
SVARO, FE ;
SVARC, FE .
JOURNAL OF SOLUTION CHEMISTRY, 1995, 24 (02) :121-132
[4]  
CORTI HR, 1979, J SOLUTION CHEM, V12, P897
[5]  
DARKEN LS, 1966, BER BUNSEN PHYS CHEM, V70, P1120
[6]  
DUDZIAK KH, 1966, BERICH BUNSEN GESELL, V70, P1120
[7]   HIGH-PRESSURE ELECTROLYTE CONDUCTIVITY OF THE HOMOGENEOUS, FLUID WATER-SODIUM HYDROXIDE SYSTEM TO 400-DEGREES-C AND 3000 BAR [J].
EBERZ, A ;
FRANCK, EU .
BERICHTE DER BUNSEN-GESELLSCHAFT-PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 1995, 99 (09) :1091-1103
[8]   SELF-DISSOCIATION AND PROTONIC CHARGE TRANSPORT IN WATER AND ICE [J].
EIGEN, M ;
DEMAEYER, L .
PROCEEDINGS OF THE ROYAL SOCIETY OF LONDON SERIES A-MATHEMATICAL AND PHYSICAL SCIENCES, 1958, 247 (1251) :505-533
[9]  
ERDEYGRUZ T, 1977, MOD ASPECT ELECTROC, V12, P1
[10]  
Fernandez-Prini R., 1973, Physical Chemistry of Organic Solvent Systems, P525