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SEPARATION AND PURIFICATION TECHNOLOGY · 2024 · IF 8.1

Selective dissolution and separation of lanthanides and actinides from spent nuclear fuel using inorganic salt solutions: A sustainable approach

Xilin Gao,Anting Ding,Yuxin Li,Chuanying Liu,Chengliang Xiao

Efficient utilization of uranium resources and minimization of nuclear waste are critical challenges for the sustainable development of nuclear energy. The separation of actinides (An) from lanthanides (Ln) is essential to reduce the impact of neutron poisons and enhance the efficiency of Partitioning & Transmutation (P&T) processes. In this study, we propose the use of a concentrated AlCl 3 solution as a selective leaching agent to separate Ln from An in spent nuclear fuel (SNF). At a mass ratio of 1:15, the AlCl 3 solution effectively dissolves nearly 100 % of lanthanide oxides from simulated SNF at 75 °C, while the coexisting actinide oxides remain largely insoluble. The high separation factors between Ln 2 O 3 and AnO 2 (average of 1630 for Ln/U and 490 for Ln/Th) provide a novel and efficient approach for the selective separation of lanthanides from SNF. The lanthanides are subsequently recovered through oxalic acid precipitation and calcination to produce Ln 2 O 3 . Based on our characterization results, the primary driving force for the dissolution of Ln 2 O 3 is the acidity of the H 2 O-AlCl 3 system, with the lattice energies of oxides identified as the key factor affecting the differential dissolution of Ln(III) and U/Th with higher valent under identical conditions. This selective dissolution and separation process using AlCl 3 solution presents a highly efficient method for the removal of lanthanides from SNF and improves the utilization of nuclear fission products. With its mild operating conditions and reduced environmental impact, this method offers a promising approach for the recovery of rare earth elements from nuclear waste and other secondary resources.

CAS / MDL: 7784-13-6 144-62-7
研究领域: 核化学与放射化学 · 环境科学 · 材料科学
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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH · 2022 · IF 4.326

Preparation of α-High-Strength Hemihydrate from Flue Gas Desulfurization Gypsum in AlCl3–MgCl2 Solution at Atmospheric Pressure

Shuaifeng Liu,Edouard Asselin,Zhibao Li

An industrially feasible process was proposed to produce α-calcium sulfate hemihydrate (α-HH) from FGD gypsum without any additives. In this process, an AlCl3 solution was used to promote the conversion of calcium sulfate dihydrate (DH) to hexagonal prismatic α-HH with high strength at atmospheric pressure. The phase transition kinetics of FGD gypsum was experimentally investigated under conditions: AlCl3 (2–2.5 m), MgCl2 (0–0.4 m) existing in raw FGD gypsum, and the solid–liquid ratio (or solid content %) range of 0.1–2 at 363 K. It was found that increasing the concentrations of MgCl2 in AlCl3 solution accelerated the conversion. The uniform large hexagonal prism HH product was obtained at the folowing optimal conditions: 2.5 mol/kg AlCl3, 0.4 mol/kg MgCl2, solid–liquid ratio of 2, and equilibration time of 2 h at 363 K. The phase diagram of the AlCl3-MgCl2-H2O system was determined by measuring solubility of solids. The E-NRTL activity model was used to construct the phase transition diagram of CaSO4 in AlCl3–MgCl2 media and to judge the stable range of DH and HH.

研究领域: 材料科学 · 化学工程
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