A mechanistic approach of chromium (VI) adsorption onto manganese oxides and boehmite.

• Cr(VI) adsorption has been studied using manganese oxides and boehmite. • Langmuir equation could correlate Cr(VI) adsorption data nicely. • Birnessite showed maximum adsorption at pH 2 while others showed a maximum in the pH range of 5.8–8.2. • Cr(VI) adsorption involved more than one type of reaction. • Formation of both outer and inner-sphere Cr(VI) complexes depending on pH. The concentration of chromium (VI) in the soil is an important environmental concern due to its mobility and acute toxicity. Due to its toxicity, removal of this species is very important. The mobility of Cr(VI) is highly governed by its adsorption onto the mineral surfaces. Manganese oxides are naturally-occurring scavengers and have a significant influence on the distribution, and transport of chromate species. Thus, to understand the fate of chromate species and its removal process, it is important to study chromium (VI) adsorption. In this study, birnessite (δ-MnO 2), pyrolusite (β-MnO 2), hausmannite (Mn 3 O 4), manganite (γ-MnOOH), boehmite (γ-AlOOH), and Mn-Al binary oxide was used as adsorbents to adsorb Cr(VI) over a range of solution pH and initial Cr(VI) concentrations. A combined approach using the Langmuir and Freundlich models, proton stoichiometry and surface complexation model (SCM) have been used to describe the probable Cr(VI) adsorption process. Birnessite was the most potent adsorbent at low pH. The Langmuir model could describe the equilibrium isotherm data well, suggesting a uniform surface nature. Proton stoichiometry indicated that Cr(VI) adsorption involved more than one type of reaction. The findings confirm that Cr(VI) species bind to functional groups by the inner- and outer-sphere chromate complexes, with the extent of binding dependent on solution pH. The study presented herein can be applied to soils with a variety of surface properties, pH, and Cr (VI) concentrations. The study further advances our understanding of the interaction between Cr(VI) and minerals at the solid-water interface. [ABSTRACT FROM AUTHOR]