Selective Capacitive Recovery of Rare-Earth Ions from Wastewater over Phosphorus-Modified TiO2 Cathodes via an Electro-Adsorption Process.

Large amounts of wastewater containing low-concentration (<10 ppm) rare-earth ions (REIs) are discharged annually in China's rare-earth mining and processing industry, resulting in severe environmental pollution and economic losses. Hence, achieving efficient selective recovery of low-concentration REIs from REIs-containing wastewater is essential for environmental protection and resource recovery. In this study, a pseudocapacitance system was designed for highly efficient capacitive selective recovery of REIs from wastewater using the titanium dioxide/P/C (TiO2/P/C) composite electrode, which exhibited over 99% recovery efficiency for REIs, such as Eu3+, Dy3+, Tb3+, and Lu3+ in mixed solution. This system maintained high efficiency and more than 90 times the enrichment concentration of REIs even after 100 cycles. Ti4+ of TiO2 was reduced to Ti3+ of Ti3O5 under forward voltage in the system, which trapped the electrons of phosphorus site and caused it to be oxidized to phosphate with a strong affinity for REIs, thus improving the selectivity of REIs. Under reverse voltage, Ti3O5 was oxidized to TiO2, which transferred electrons to phosphate and transformed to the phosphorus site, resulting in the desorption and enrichment of REIs and the regeneration of the electrode. This study provides a promising method for the efficient recovery of REIs from wastewater.

One-step removal of high-concentration arsenic from wastewater to form Johnbaumite using arsenic-bearing gypsum.

High-level arsenic-containing wastewater (HAW) causes serious environmental pollution. Chemical precipitation is the most widely used technology for treating HAW. However, chemical precipitation generates huge amounts of hazardous solid wastes, which leads to secondary pollution. In this work, an efficient method, producing no secondary pollution was developed for one-step complete removal of As(V) from HAW using a hazardous solid waste namely arsenic-bearing gypsum (ABG). After the treatment, ABG was transformed into highly stable and environment-friendly mineral Johnbaumite. Meanwhile, the arsenic concentration in the wastewater decreased from 10,000 mg L-1 to 0.22 mg L-1 under optimized hydrothermal conditions (ABG dosage of 50 g L-1, solution pH of 13.5, temperature of 150 °C for 12 h). The mechanism mainly included the following processes: (i) The phase transformation of ABG resulted in the release of calcium and hydrogen arsenate ions in ABG, (ii) Hydrogen arsenate ions transformed into arsenate ions in alkaline environment, and (iii) Under alkaline conditions, calcium ions combined with arsenate ions to form Johnbaumite, whereas the hydrothermal conditions accelerated the crystal growth of Johnbaumite. This study provides a new idea for the synchronous treatment of toxic heavy metal-containing wastewaters and hazardous solid wastes.