Artículos de revistas
Arsenate adsorption at the sediment-water interface: Sorption experiments and modelling
Fecha
2012-01Registro en:
Borgnino Bianchi, Laura Carolina; de Pauli, Carlos Primo; Depetris Gallino, Pedro Jose; Arsenate adsorption at the sediment-water interface: Sorption experiments and modelling; Springer; Environmental Earth Sciences; 65; 2; 1-2012; 441-451
1866-6299
CONICET Digital
CONICET
Autor
Borgnino Bianchi, Laura Carolina
de Pauli, Carlos Primo
Depetris Gallino, Pedro Jose
Resumen
Arsenate adsorption was studied in three clastic sediments, as a function of solution pH (4.0-9.0) and arsenate concentration. Using known mineral values, protolytic constants obtained from the literature and K ads values (obtained by fitting experimental adsorption data with empirical adsorption model), the constant capacitance surface complexation model was used to explain the adsorption behavior. The experimental and modelling approaches indicate that arsenate adsorption increases with increased pH, exhibiting a maximum adsorption value before decreasing at higher pH. Per unit mass, sample S 3 (smectite-quartz/muscovite-illite sample) adsorbs more arsenate in the pH range 5-8. 5, with 98% of sites occupied at pH 6. S 1 and S 2 have less adsorption capacity with maxima adsorption in the pH ranges of 6-8.5 and 4-6, respectively. The calculation of saturation indices by PHREEQC at different pH reveals that the solution was undersaturated with respect to aluminum arsenate (AlAsO 42H 2O), scorodite (FeAsO 42H 2O), brucite and silica, and supersaturated with respect to gibbsite, kaolinite, illite and montmorillonite (for S 3 sample). Increased arsenate concentration (in isotherm experiments) may not produce new solid phases, such as AlAsO 42H 2O and/or FeAsO 42H 2O. © 2011 Springer-Verlag.