Objectif The objective is to make progress in the area of the fundamental physical and chemical processes that govern pollutant behaviour in the soil system, integrate the new knowledge with existing knowledge and apply it to soil samples, soil solutions and transport in soil columns and aquifers The effect of calcium competition on cadmium binding on humic acids has been measured using voltammetric methods. Adsorption of humic acids on the mercury aqueous solution interface has been studied. Copper binding to humic acids was measured by ion selective electrode at pH 4, 6 and 8 with copper activities varying from 1E-3 to 1E-14 M. 10 different types of iron oxides were synthesized and characterized for specific surface area and porosity. Binding of cadmium on several of these oxides was measured as a function of pH and metal ion activity. The charging characteristics of these same oxides were determined as a function of pH and ionic strength. Although the charging properties varied considerably for the various materials, the cadmium binding behaviour was quite similar. Adsorption of humic acid on hematite was studied as a function of pH, indicating increased adsorption with decreasing pH. Cadmium binding on 2 different soils was measured using pH stat and a cadmium selective electrode, allowing the exchange stochiometry between hydrogen and cadmium ions to be established. A collection of 28 different soils was intensively characterized and the soil extracts analyzed for approximately 50 elements. A theoretical analysis was made on wetting front instability leading to fingering wetting, profiles. This type of water movement can also affect solute transport in the field. The combination of physical and chemical heterogeneity on solute transport was analysed. A new analytical mathematical solution for this type of problem was derived and results were compared with those of numerical methods. The longitudinal spreading of the retarded plumes is greatly affected by the interplay of physical and chemical heterogeneity. Transverse spreading is unaffected by chemical heterogeneity.In the research project 6 major parts can be distinguished as follows. Measurement and modelling of the interaction of cadmium, zinc, hydrogen and calcium with several purified soil humic and fulvic acids. Measurement and interpretation of the metal speciation in soil extracts using water and 0.01 M calcium chloride as extractants. Preparation and characterization of iron oxides with different surface structures. Measurement and modelling of specific ion adsorption (both cations and anions) on these iron oxides. Characterization of iron oxides in soils, measurement and modelling of ion adsorption to iron oxides in soils. Measurement and interpretation of the interaction of purified humic and fulvic acids with mineral surfaces (metal oxides, clay) in the presence of variable concentrations of metal ions under a series of environmental conditions (eg pH, salt level). Measurement and modelling of metal speciation in these systems. Development of methods to determine the type and number of reactive sites in soils. Measurement of metal adsorption to soils under a series of conditions, test of the applicability of physical chemical adsorption models for estimating metal speciation in soils. Integration of existing and newly developed knowledge with respect to chemical processes in soil (adsorption to several reactive phases, complexation, ion exchange, precipitation) in a multi component chemical model that can be coupled to a transport algorithm. Finally, measurement of heavy metal transport (cadmium and zinc) through soil and aquifer materials. Modelling with the multicomponent transport model to validate parameter sets obtained in the second, third and fourth parts. Extension of measurements and modelling using heterogeneous columns. In situ measurement of tracer and reacting chemical transport in unsaturated soil and in aquifers to characterize preferential flow in natural heterogeneous systems. Modelling with deterministic and stochastic models for soil and aquifers. Champ scientifique natural scienceschemical sciencesinorganic chemistryinorganic compoundsnatural scienceschemical sciencesinorganic chemistrytransition metalsnatural scienceschemical sciencesinorganic chemistryalkaline earth metalsnatural sciencesmathematicsapplied mathematicsnumerical analysis Programme(s) FP2-STEP - Two specific research and technological development programmes (EEC) in the field of the environment STEP/EPOCH - STEP -, 1989-1992 Thème(s) Data not available Appel à propositions Data not available Régime de financement CSC - Cost-sharing contracts Coordinateur Landbouwuniversiteit Wageningen Contribution de l’UE Aucune donnée Adresse 10,Dreijenplein 6703 HB Wageningen Pays-Bas Voir sur la carte Coût total Aucune donnée Participants (6) Trier par ordre alphabétique Trier par contribution de l’UE Tout développer Tout réduire Instituto Superior Técnico Portugal Contribution de l’UE Aucune donnée Adresse Av.Rovisco Pais 1000 Lisboa Voir sur la carte Coût total Aucune donnée Junta de Andalucía Espagne Contribution de l’UE Aucune donnée Adresse 1,Avda de la Borbolla 41004 Sevilla Voir sur la carte Coût total Aucune donnée Landbouwuniversiteit Wageningen Pays-Bas Contribution de l’UE Aucune donnée Adresse 6,Dreijenplein 6703 HB Wageningen Voir sur la carte Coût total Aucune donnée Natural Environment Research Council Royaume-Uni Contribution de l’UE Aucune donnée Adresse NG12 5GG Nottingham Voir sur la carte Coût total Aucune donnée TECHNICAL UNIVERSITY OF MUNICH Allemagne Contribution de l’UE Aucune donnée Adresse Hohenbachernstraße 85350 FREISING Voir sur la carte Coût total Aucune donnée UNIVERSITÀ DEGLI STUDI DI TRENTO Italie Contribution de l’UE Aucune donnée Adresse Via Mesiano di Povo 77 38100 TRENTO Voir sur la carte Coût total Aucune donnée