Prediction of Activity Coefficients for Uni-univalent Electrolytes in Pure Aqueous Solution

被引:6
作者
Partanen, Jakko I. [1 ]
Salmimies, Riina K. [2 ]
Partanen, Lauri J. [3 ]
Louhi-Kultanen, Marjatta [2 ]
机构
[1] Lappeenranta Univ Technol, Phys Chem Lab, Dept Chem Technol, Fac Technol, FIN-53851 Lappeenranta, Finland
[2] Lappeenranta Univ Technol, Lab Separat Technol, Dept Chem Technol, Fac Technol, FIN-53851 Lappeenranta, Finland
[3] Univ Helsinki, Phys Chem Lab, Dept Chem, FIN-00014 Helsinki, Finland
关键词
Activity coefficients; Aqueous solutions; Binary Solutions; Modeling; Thermodynamics; THERMODYNAMIC ACTIVITY QUANTITIES; POTASSIUM-CHLORIDE SOLUTIONS; VAPOR-PRESSURE MEASUREMENTS; STANDARD POTENTIALS; AMALGAM ELECTRODE; DISSOCIATION-CONSTANTS; OSMOTIC COEFFICIENTS; SIT PARAMETERS; 298.15; K; 25-DEGREES-C;
D O I
10.1002/ceat.200900617
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Parameter-free activity coefficient equations were tested in addition to those containing one, two, three or four electrolyte-dependent parameters with the experimental activity coefficients obtained from the literature data for aqueous solutions of the following electrolytes at 298.15 K: KCl, NaCl, RbCl, KBr, RbBr, CsBr, KI, RbI, KNO(3), and KH(2)PO(4). The experimental activity coefficients of each electrolyte considered can be reproduced within the uncertainty of the measurements up to the molality of the saturated solution by using a three-parameter equation of the extended Huckel type. The best Huckel equations are given for all electrolytes in question. The results from the present studies reveal that the parameter-free equations can be reliably used in thermodynamic studies only for very dilute electrolyte solutions. On the other hand, in most cases, a good agreement with the experimental data is obtained with the one-parameter equations of Bromley [14] and Kusik and Meissner [13], with the two-parameter equation of Bretti et al. [15], and with the three- or four-parameter equation of Hamer and Wu [19] in addition to the three-parameter Pitzer equation [23], with almost all parameter values suggested in the literature. In several cases, these equations seem to apply to much higher molalities than those used in the parameter estimations. Therefore, the best of these equations may have important applications in calculations associated with the dissolution and crystallization processes of these salts.
引用
收藏
页码:730 / 742
页数:13
相关论文
共 48 条
[1]   THE DIELECTRIC-CONSTANT OF WATER AND DEBYE-HUCKEL LIMITING LAW SLOPES [J].
ARCHER, DG ;
WANG, PM .
JOURNAL OF PHYSICAL AND CHEMICAL REFERENCE DATA, 1990, 19 (02) :371-411
[2]   THERMODYNAMIC PROPERTIES OF STRONG ELECTROLYTES IN AQUEOUS-SOLUTIONS [J].
BROMLEY, LA .
AICHE JOURNAL, 1973, 19 (02) :313-320
[3]   Measurement of pH. Definition, standards, and procedures [J].
Buck, RP ;
Rondinini, S ;
Covington, AK ;
Baucke, FGK ;
Brett, CMA ;
Camoes, MF ;
Milton, MJT ;
Mussini, T ;
Naumann, R ;
Pratt, KW ;
Spitzer, P ;
Wilson, GS .
PURE AND APPLIED CHEMISTRY, 2002, 74 (11) :2169-2200
[4]   Thermodynamics of formation of double salts and mixed crystals from aqueous solutions [J].
Christov, C .
JOURNAL OF CHEMICAL THERMODYNAMICS, 2005, 37 (10) :1036-1060
[5]   CALCULATION OF THE GIBBS ENERGY OF MIXING IN CRYSTALS USING PITZERS MODEL [J].
CHRISTOV, C ;
PETRENKO, S ;
BALAREW, C ;
VALYASHKO, V .
JOURNAL OF SOLUTION CHEMISTRY, 1994, 23 (07) :795-812
[6]   DEFINITION OF PH SCALES, STANDARD REFERENCE VALUES, MEASUREMENT OF PH AND RELATED TERMINOLOGY - (RECOMMENDATIONS 1984) [J].
COVINGTON, AK ;
BATES, RG ;
DURST, RA .
PURE AND APPLIED CHEMISTRY, 1985, 57 (03) :531-542
[7]   SIT Parameters for the Dependence of (Poly)carboxylate Activity Coefficients on Ionic Strength in (C2H4)4NIaq (0 ≤ I ≤ 1.2 mol•kg-1) and (CH3)4NClaq (0 ≤ 1 ≤ 3.9 mol•kg-1) in the temperature range 278 ≤ T ≤ 328 K and correlation with Pitzer parameters [J].
Crea, Francesco ;
De Stefano, Concetta ;
Foti, Claudia ;
Sanunartano, Silvio .
JOURNAL OF CHEMICAL AND ENGINEERING DATA, 2007, 52 (06) :2195-2203
[8]   Sit parameters for 1:2 electrolytes and correlation with Pitzer coefficients [J].
Crea, Francesco ;
Foti, Claudia ;
De Stefano, Concetta ;
Sammartano, Silvio .
ANNALI DI CHIMICA, 2007, 97 (1-2) :85-95
[9]   The extent of dissociation of salts in water. Part VIII. An equation for the mean ionic activity coefficient of an electroltye in water, and a revision of the dissociation constants of some sulphates [J].
Davies, CW .
JOURNAL OF THE CHEMICAL SOCIETY, 1938, :2093-2098
[10]  
DAVIES CW, 1962, IONIC ASS