ABSTRACT
We investigated the feasibility of using FeS-coated alumina and silica for permeable reactive barrier (PRB) applications. By both coated materials, Cr(VI) was reduced to Cr(III), which was immobilized via surface complexation/precipitation at acidic pH, and bulk precipitation at neutral to basic pH. Both pH and surface coating density (the amount of FeS deposits per unit surface area of a supporting matrix) controlled Cr(VI) reduction capacity and [Cr,Fe](OH)3 composition. The reduction was higher at acidic pH due to lower passivation, as evidenced by the increased production of Fe(III) (oxyhydr)oxides over Fe(II)-Fe(III) phases. The coated alumina, despite the lower amount of FeS deposits than the coated silica, showed greater reduction capacities due to its higher surface coating density, which made Fe(III) closer together to favor Fe(III) (oxyhydr)oxide formation. Since Cr(III) was preferentially substituted for Fe(III) in Fe(III) (oxyhydr)oxides, lower pH and higher surface coating density led to lower Cr fractions in [Cr,Fe](OH)3 because of the increased production of Fe(III) (oxyhydr)oxides. Given that Cr-poor [Cr,Fe](OH)3 is more resistant to re-oxidation, FeS-coated alumina is better for PRB applications. This study reveals the significance of the surface coating density when evaluating the effectiveness of coated materials in redox-based treatments.
