Ion adsorption rare-earth (IARE) ores, a strategic metal resource, are extracted by leaching with ammonium sulfate [(NH4)₂SO₄] solution, our samples have ∑REO grades of 0.032–0.079% wt%. IARE sandstone, mudstone, clay, and strongly weathered rock were selected as test materials. Surface-related physicochemical parameters were determined, and bound water was determined by volumetric flask pycnometry. For each IARE lithology, we also obtained particle size distributions and evaluated bound water variation in (NH₄)₂SO₄ solutions at 0, 1, 2, and 3 wt%. Based on the Gouy–Chapman theory, the relationship between the surface bound water and solution concentration, as well as the surface charge of IARE samples, and other influencing factors was explored. The experimental results show the following: ① The surface charge per unit area of four types of IARE samples, namely mudstone, sandstone, clay, and strongly weathered rock, are 0.7072 × 10⁻² mmol/m², 1.9620 × 10⁻² mmol/m², 1.5418 × 10⁻² mmol/m², and 2.1003 × 10⁻² mmol/m², respectively, with strongly weathered rock having the highest and mudstone having the lowest. ② As the concentration of aqueous (NH₄)₂SO₄ increases (0, 1, 2, 3 wt%), the total volume reduction in free water ∆V in the system increases, and the mass of adsorbed bound water per unit mass of IARE sample also increases. ③ As the concentration of the solution increases, the thickness of the diffusion double layer on the surface of the IARE sample is compressed, the total amount of adsorbed anions and cations on the surface increases, and the density of the surface water film also increases, leading to a corresponding increase in the quality of adsorbed bound water. ④ Under the same solution concentration, the variation trend of adsorbed bound water mass per unit area of IARE samples is strongly weathered rock > sandstone > clay > mudstone, which is consistent with the trend of surface charge per unit area of IARE samples. A higher lixiviant concentration increases bound water, shrinks the effective pore throats of the ore body, reduces hydraulic conductivity, and consequently diminishes leaching efficiency.

The efficient recovery of rare earth elements (REEs) from low-concentration mine tailwater is crucial for resource sustainability. In this study, a novel composite adsorbent, sesame stalk biochar-supported zirconium phosphate (sBC/ZrP), was synthesized for the selective adsorption and recovery of La³⁺ as a representative REE. The material was characterized using SEM-EDS, BET, XRD, FTIR, and XPS. Batch adsorption experiments were conducted to evaluate the effects of pH, coexisting ions, and the adsorption kinetics and thermodynamics. The results showed that sBC/ZrP exhibited a high adsorption capacity (up to 185.83 mg/g at 35 °C for 4 h) and strong selectivity for La³⁺, particularly in the presence of common competing cations, although Al³⁺ demonstrated significant interference. The adsorption process followed pseudo-second-order kinetics and the Langmuir isotherm model, indicating monolayer chemisorption, and was determined to be spontaneous and endothermic. The material maintained over 90% adsorption efficiency after five consecutive adsorption–desorption cycles. The mechanism primarily involved complexation of La³⁺ with the P-OH and Zr-O groups on the composite. This work demonstrates that sBC/ZrP is a highly efficient, stable, and reusable adsorbent with significant potential for the recovery of REEs from mining tailwater.