Solidification performances of contaminants by red mud-based cementitious paste filling material and leaching behavior of contaminants in different pH and redox potential environments

Considering the urgent need for disposal of red mud and the comprehensive treatment of coal mined-out areas, this paper presented red mud-based cementitious paste filling material (RMFM) to achieve the purpose of green filling treatment. However, the solidification performance of alkaline RMFM for contaminants can be affected when in contact with acid goaf water in practice, which may in turn causes secondary pollution to the surroundings. The leaching tests of RMFM under different pH and redox potential (Eh) conditions were designed to investigate the effects of environmental elements on the solidification performance of RMFM, and primarily investigated the treatment effectiveness of RMFM on goaf water. The test results manifest that the acidic and oxidizing environments could damage the hydration products generated by alkali and sulfate activation, thus affecting the solidification performance, while the alkaline and reducing environments could effectively prevent the release of the contaminants by enhancing the degree of alkali activation and inhibiting oxidation acid forming process. In the possible exposure environment, RMFM could effectively stabilize its own pollutants without secondary pollution. In addition, the powder RMFM samples had significant removal effects on heavy metals, the values of Cu, Pb, and As removal efficiency all reached more than 96.15%.

Influence of Chemical Operation on the Electrocatalytic Activity of Ba0.5Sr0.5Co0.8Fe0.2O3−δ for the Oxygen Evolution Reaction

Ba0.5Sr0.5Co0.8Fe0.2O3−δ (BSCF) is a promising electrocatalyst for the oxygen evolution reaction (OER) in alkaline solution. The OER activities of BSCF are gradually enhanced by prolonging the duration of electrochemical operation at OER potentials, but the underlying cause is not fully understood. In this study, we investigated the role of chemical operation, equivalent to immersion in alkaline solution, in the time-course of OER enhancement of BSCF. Interestingly, the time-course OER enhancement of BSCF was promoted not only by electrochemical operation, which corresponds to potential cycling in the OER region, but also by chemical operation. In situ Raman measurements clarified that chemical operation had a lower rate of surface amorphization than electrochemical operation. On the other hand, the leaching behavior of A-site cations was comparable between chemical and electrochemical operations. Since the OER activity of BSCF was stabilized by saturating the electrolyte with Ba2+, “chemical” A-site leaching was key to inducing the time-course OER enhancement on perovskite electrocatalysts. Based on these results, we provide a fundamental understanding of the role of chemical operation in the OER properties of perovskites.