Steel slag has been proven to be an effective environment remediation media for acid neutralization, and a potential aid to mitigate acid mine drainage (AMD). Yet its acid neutralization capacity (ANC) is frequently inhibited by precipitate after a period of time, while the characteristics of the precipitate formation process are unclear yet. In this study, ANC for basic oxygen steel slag was conducted by neutralization experiments with dilute sulfuric acid (0.1 M) and real AMD. Some partially neutralized steel slag samples were determined by X-ray diffraction (XRD), scanning electron microscopy combined with an energy dispersive spectrometer (SEM-EDS), and N2 adsorption tests to investigate the potential formation process of the precipitate. The results indicated that Ca-bearing constitutes leaching and sulfate formation were two main reactions throughout the neutralization process. A prominent transition turning point from leaching to precipitate was at about 40% of the neutralization process. Tricalcium silicate (Ca3SiO5) played a dominant role in the alkalinity-releasing stage among Ca-bearing components, while the new-formed well crystalline CaSO4 changed the microstructure of steel slag and further hindered alkaline components releasing. For steel slag of 200 mesh size, the ANC value for the steel slag sample was 8.23 mmol H+/g when dilute sulfate acid was used. Neutralization experiments conducted by real AMD confirmed that the steel slag ANC was also influenced by the high contaminants, such as Fe2+, due to the hydroxides precipitate reactions except for sulfate formation reactions.
Keywords: acid mine drainage; acid neutralization capacity; alkaline; steel slag.