Metal-Impregnated Petroleum Coke-Derived Activated Carbon for the Adsorption of Arsenic in Acidic Waters

Abstract

The efficacy of metal-impregnated petroleum coke (PC) activated carbon for the adsorption of arsenite and arsenate in acidic waters is investigated in this study. Unmodified PC activated carbon, FeCl3-loaded activated carbon, KMnO4-loaded activated carbon, and a mixed FeCl3–KMnO4-loaded activated carbon were used for evaluation. The surface characteristics of the activated carbons before and after arsenic adsorption were analyzed by X-ray photoelectron spectroscopy (XPS). Arsenate adsorption was significantly improved by the addition of an iron–manganese-loaded activated carbon, increasing adsorption from 8.12 to 50.93%. Oxidation–reduction reactions are proposed based on the observed arsenic 2p3/2, iron 2p3/2, and manganese 2p3/2 XPS peaks. While iron in the iron-loaded activated carbon is not acting as the reducing agent, it is acting as a conductor for the flow of electrons from the activated carbon to the arsenic for reduction to take place prior to the physisorption of the arsenic. In the manganese-loaded activated carbon, manganese acts as the reducing agent for arsenic prior to arsenic adsorption to the surface through physisorption. XPS of the post-arsenic(V) exposure samples showed that the Fe2O3 species were reduced from 32.18 to 1.66% in the FeMn-loaded sample, while the FeOOH species were increased from 53.16 to 81.71%. Similarly, MnO in the FeMn-loaded activated carbon dropped from 26.82 to 15.40%, while MnOOH and MnO2 increased from 39.98 and 33.20 to 43.96 and 40.64%, respectively. This is consistent with the proposed mechanism. The adsorption of arsenite was also evaluated to show that the modification of the activated carbon adsorbed not only the arsenic(V) species but also the more toxic arsenic(III) species without the need for oxidation of the arsenic prior to adsorption.