Copper, Chromium, and Arsenic Adsorption and Equilibrium Modeling in An Iron-Oxide-Coated Sand, Background Electrolyte System

Abstract

The adsorption of copper, chromate, and arsenate (CCA)onto iron-oxide-coated sand (IOCS) was examined insingle-metal and mixed-metal systems. Copper andarsenate were strongly adsorbed or formed inner-spheresurface complexes with the IOCS surface while chromatewas weakly adsorbed or formed an outer-sphere surfacecomplex with the IOCS surface. Copper adsorption byIOCS slightly increased in the presence of arsenatebut was not affected by the presence of chromate. Arsenate adsorption was not affected by the presenceof copper and/or chromate. Chromate adsorptionincreased in the presence of copper by the combinationof electrostatic effects and possiblesurface-copper-chromate ternary complex formation. The presence of arsenate significantly decreasedchromate adsorption due to competition for adsorptionsites and electrostatic effects. Using inner-spheresurface complexation constants for copper and arsenateand outer-sphere surface complexation constants forchromate, the triple-layer model (TLM) was successfulin describing adsorption of copper, chromate, andarsenate in single-solute systems. The modelindicated that each metal uses a different number ofadsorption sites. For CCA metals-IOCS systems, theequilibrium constants determined from single-solutesystems were not able to predict adsorption frommulti-solute systems. The TLM does not currentlyaccount for the heterogeneity of oxide surface sitesand the formation of ternary complexes and/or solidphases that do not exist in single-solute systems.