The superior adsorption capacity of biogenic α-Mn2O3 in comparison to chemogenic α-Mn2O3 for five divalent heavy metal cations and the adsorption mechanism of biogenic α-Mn2O3: Experimental and DFT investigations

Abstract

Manganese oxides play a crucial role in the adsorption of heavy metals in the environment. However, there is currently a lack of information regarding the comparative adsorption efficiency of heavy metals between biogenic and chemogenic manganese oxides. In this work, we compared the adsorption performance of biogenic and chemogenic α-Mn2O3 towards Pb(II), Cd(II), Cu(II), Zn(II) and Ni(II). Mineral characterization analyses revealed that biogenic α-Mn2O3 exhibited a polycrystalline nature, whereas chemogenic α-Mn2O3 displayed a monocrystalline nature with a lower impurity content compared to biogenic α-Mn2O3. Under acidic conditions, biogenic α-Mn2O3 demonstrated a significantly higher adsorption capacity, ranging from 3 to 6 times greater than its chemogenic counterpart, within an initial heavy metal concentration range of 0.2–1.0 mM. This superiority can be attributed to the presence of more abundant functional groups and a greater content of hydroxyl O species on the surface of biogenic α-Mn2O3 in comparison to chemogenic α-Mn2O3. During the adsorption process of biogenic α-Mn2O3, there were observed ionic exchanges between Mn(II) and these cations. More importantly, biogenic α-Mn2O3 bound with these cations probably through the formation of -O/OH/S complexes. The adsorption selectivity of biogenic α-Mn2O3 towards the five heavy metals was experimentally determined to follow the order of Ni(II) > Pb(II) > Cu(II) > Zn(II) > Cd(II). The electronic interaction between biogenic α-Mn2O3 and these cations indicated that Ni(II), Pb(II) and Cu(II) were more likely to share electrons with O atoms on the surface of biogenic α-Mn2O3 compared to Zn(II) and Cd(II).