Modeling lead adsorption on clays by models with and without electrostatic terms

被引:25
作者
Majone, M [1 ]
Papini, MP [1 ]
Rolle, E [1 ]
机构
[1] UNIV ROMA LA SAPIENZA,DEPT ENVIRONM ENGN,I-00184 ROME,ITALY
关键词
adsorption models; electrostatic models; heterogeneity; lead; clays;
D O I
10.1006/jcis.1996.0232
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The research describes the adsorption of heavy metals (lead) on clay minerals (kaolinite) as function of different experimental conditions, The lead adsorption was investigated as function of pH and ionic strength at several initial lead concentrations, The adsorption of proton and sodium (obtained by titration curves and negative surface charge measurements, respectively) was also investigated as function of pH, AU experimental variables were simultaneously accounted for by using the multivariate nonlinear regression of data, according to different models including or not including electrostatic interactions, The adsorption of lead, proton, and sodium on the clay was successfully described by a three-layer electrostatic model considering two discrete types of adsorption sites (with fixed and variable charge, respectively) and the additional effect of the heterogeneity of each site (in terms of continuous distribution of the affinity constants), Confident estimates were obtained for the site concentrations (adsorption maxima) and the heterogeneity parameters. The sites with fixed and variable charge were found to be 40 and 60% of the total, respectively. Both of them contribute to the lead adsorption in proportions which highly depend on the pH, The heterogeneity parameters of both sites have low values which underline the high influence of the continuous distribution of the affinity constants, The diffuse layer potential was also well estimated. It depends mainly on the ionic strength and it is quite different from the measured zeta potential (about one order of magnitude more negative). To consider simultaneously all experimental variables by a multivariate approach appeared to be very important for an accurate modeling, If only the lead adsorption was taken into account at a single ionic strength, the electrostatic effects could be neglected with no practical difference on the calculated behavior. (C) 1996 Academic Press, Inc.
引用
收藏
页码:412 / 425
页数:14
相关论文
共 30 条
[1]  
Baes C.F., 1976, HYDROLYSIS CATIONS
[2]   REACTION OF ANIONS AND CATIONS WITH VARIABLE-CHARGE SOILS [J].
BARROW, NJ .
ADVANCES IN AGRONOMY, 1985, 38 :183-230
[3]   OBJECTIVE METHOD FOR FITTING MODELS OF ION ADSORPTION ON VARIABLE CHARGE SURFACES [J].
BARROW, NJ ;
BOWDEN, JW ;
POSNER, AM ;
QUIRK, JP .
AUSTRALIAN JOURNAL OF SOIL RESEARCH, 1980, 18 (01) :37-47
[4]   DESCRIBING THE ADSORPTION OF COPPER, ZINC AND LEAD ON A VARIABLE CHARGE MINERAL SURFACE [J].
BARROW, NJ ;
BOWDEN, JW ;
POSNER, AM ;
QUIRK, JP .
AUSTRALIAN JOURNAL OF SOIL RESEARCH, 1981, 19 (04) :309-321
[5]   SURFACE-CHARGE ON KAOLINITES IN AQUEOUS SUSPENSION [J].
BOLLAND, MDA ;
POSNER, AM ;
QUIRK, JP .
AUSTRALIAN JOURNAL OF SOIL RESEARCH, 1976, 14 (02) :197-216
[6]  
BOWDEN JW, 1977, AUST J SOIL RES, V15, P121, DOI 10.1071/SR9770121c
[7]   THE EXCHANGE ADSORPTION OF IONS FROM AQUEOUS SOLUTIONS BY ORGANIC ZEOLITES .1. ION-EXCHANGE EQUILIBRIA [J].
BOYD, GE ;
SCHUBERT, J ;
ADAMSON, AW .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1947, 69 (11) :2818-2829
[8]  
Davies C., 1962, ION ASS
[9]   SURFACE IONIZATION AND COMPLEXATION AT OXIDE-WATER INTERFACE .1. COMPUTATION OF ELECTRICAL DOUBLE-LAYER PROPERTIES IN SIMPLE ELECTROLYTES [J].
DAVIS, JA ;
JAMES, RO ;
LECKIE, JO .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1978, 63 (03) :480-499
[10]   THERMODYNAMIC DERIVATION OF EQUATIONS OF THE LANGMUIR TYPE FOR ION EQUILIBRIA IN SOILS [J].
ELPRINCE, AM ;
SPOSITO, G .
SOIL SCIENCE SOCIETY OF AMERICA JOURNAL, 1981, 45 (02) :277-282