This study focused on the development of mesoporous silica microspheres with controllable mesopores for the efficient removal of uranium from nuclear waste. Utilizing n-dodecylamine as a structure-directing agent and di(2-ethylhexyl)phosphoric acid (HDEHP) as a co-templating agent, we achieved the synthesis of large silica microspheres (10–100 µm) with uniform mesopores. The incorporated HDEHP served as both a swelling agent and a phosphate-functionalization reagent, facilitating the adsorption of bulky organic uranium sequestration agents. Our approach circumvented the need for high-temperature calcination and extensive use of organic solvents, making it an environmentally friendly and cost-effective alternative. The synthesized silica microspheres demonstrated superior adsorption capacity for uranyl ions, which was attributed to their large pore size and high surface area. The adsorption isotherms, well-fitted to the Langmuir model, suggested a maximum adsorption capacity of 136 mg g−1 at pH 4.0 with a uranium concentration of 100 mg L−1 to maintain a stable soluble phase. However, many studies have often overlooked solid-phase formation due to hydrolysis, which can overestimate the adsorption capacity. In addition, the particle size range enabled easy recovery through low-g-force centrifugation or natural sedimentation. This study highlighted the potential of phosphate-functionalized mesoporous silica microspheres as effective and reusable uranium adsorbents, thereby addressing both energy sustainability and environmental safety. The practical applications of these materials in uranium recovery and nuclear waste management underscore their importance in the nuclear industry.
Read full abstract