Aqueous speciation of sulfuric acid-cupric sulfate solutions

被引:110
作者
Casas, JM
Alvarez, F
Cifuentes, L
机构
[1] Univ Chile, Dept Ingn Minas, Santiago, Chile
[2] Univ Chile, Dept Ingn Quim, Santiago, Chile
关键词
chemical equilibria; copper sulfate; diffusion; electrochemistry; electrolytes; ionic conductivity; modeling; solutions; speciation; sulfuric acid; thermodynamics;
D O I
10.1016/S0009-2509(00)00421-8
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
This work presents the development and use of an ion-association multicomponent equilibrium model and the application of an ion-interaction model developed by Pitzer, to simulate the distribution and concentration of chemical species (speciation) in sulfuric acid-cupric sulfate solutions in the 0-200 g/l H2SO4 and 0-50 g/l Cu(II) concentration range and 15-70 degreesC temperature range. The model consists of a set of equations that represent the equilibrium relationships for the ionic reactions and the mass balances for the components present in the system. The effect of ionic strength was taken into account by correcting the equilibrium constants using a relationship proposed by Davies. Several species can be formed at Various pH and temperature values, the principal ones being: HSO4-, H+, SO42-, Cu2+, and CuSO4(aq). Simulations show that concentrations are highly dependent on pH. Sulfuric acid speciates mainly as bisulfate ion (HSO4-) and hydrogen ion (H+) at pH Values lower than 1. Calculations including Davies' relationship show very good agreement with experimental Values for the ionic conductivity of the solution. The conductivity of the aqueous CuSO4-H2SO4 solution decreases as cupric sulfate is added, due to the resulting decrease in hydrogen ion concentration. The model presented in this work can be applied to predict and to analyze the solution composition in electrolytic copper processes such as leaching, electrowinning and electrorefining, as well as the purification of industrial solutions used in hydrometallurgical processing. (C) 2000 Published by Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:6223 / 6234
页数:12
相关论文
共 36 条
[1]   STANDARD POTENTIAL OF COPPER AMALGAM ELECTRODE AND ACTIVITY-COEFFICIENT OF COPPER-SULFATE IN AQUEOUS-SOLUTION [J].
AJAYI, SO ;
WIGWE, FEW .
JOURNAL OF INORGANIC & NUCLEAR CHEMISTRY, 1978, 40 (05) :825-827
[2]   Computation of electrical conductivity of multicomponent aqueous systems in wide concentration and temperature ranges [J].
Anderko, A ;
Lencka, MM .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 1997, 36 (05) :1932-1943
[3]  
[Anonymous], 1991, ACTIVITY COEFFICIENT, DOI DOI 10.1201/9781351069472
[4]  
*ASPEN PLUS, 1999, 021412201 ASPEN PLUS
[5]   DETERMINATION OF THE DIFFUSION-COEFFICIENTS OF CUSO4, ZNSO4, AND NISO4 IN AQUEOUS-SOLUTION [J].
AWAKURA, Y ;
DOI, T ;
MAJIMA, H .
METALLURGICAL TRANSACTIONS B-PROCESS METALLURGY, 1988, 19 (01) :5-12
[6]   ION-INTERACTION MODEL APPLIED TO THE CUSO4-H2SO4-H2O SYSTEM AT 25-DEGREES-C [J].
BAES, CF ;
REARDON, EJ ;
MOYER, BA .
JOURNAL OF PHYSICAL CHEMISTRY, 1993, 97 (47) :12343-12348
[7]  
BALE CW, 1999, WEB SITES CHEM THERM
[8]  
Casas JM, 1999, HYDROMETALLURGY OF COPPER, P377
[9]  
CASAS JM, 1994, NATL LATIN AM METALL, V1, P1
[10]   LOCAL COMPOSITION MODEL FOR EXCESS GIBBS ENERGY OF ELECTROLYTE SYSTEMS .1. SINGLE SOLVENT, SINGLE COMPLETELY DISSOCIATED ELECTROLYTE SYSTEMS [J].
CHEN, CC ;
BRITT, HI ;
BOSTON, JF ;
EVANS, LB .
AICHE JOURNAL, 1982, 28 (04) :588-596