吸附
危险废物
涂层
浸出(土壤学)
材料科学
双功能
化学工程
聚合物
放射性废物
多孔性
废物管理
纳米技术
化学
复合材料
核化学
环境科学
抗压强度
有机化学
催化作用
土壤水分
土壤科学
工程类
作者
Siqi Ma,Shuai Fu,Hongbo Yang,Peigang He,Zongzhao Sun,Xiaoming Duan,Dechang Jia,Paolo Colombo,Yongzhi Zhou
标识
DOI:10.1016/j.jclepro.2024.140599
摘要
3D-printed geopolymer lattices (3DGPLs) have recently been considered as promising candidates for hazardous waste management due to their low cost, porous nature, and excellent environmental stability. However, the ion adsorption capacity influenced by usage conditions such as multi-ion systems and radiation remains largely unexplored. Furthermore, effective strategies to immobilize adsorbed ions for long-term disposal are still lacking. This work tackles these questions by studying the Cs+ adsorption and immobilization properties of 3DGPLs in the presence of competing ions and gamma-ray radiation. Our results reveal the inhibitory intensity of Cs+ adsorption capacity by five common metal cations in seawater, ranked in the following order: Na+ > K+ > Ca2+ > Mg2+ > Sr2+. After exposure to different doses of gamma-ray radiation, the Cs+ adsorption capacity of 3DGPLs shows no significant change, demonstrating their outstanding radiation resistance. By encapsulating the Cs-containing 3DGPL with a homologous GP coating, the Cs+ immobilization rate reaches 98.545% after leaching in NaCl solution at 60 °C for 5 days. The already-high Cs+ immobilization rate can be further increased to 99.228% by sintering treatment due to the densification effect. This study not only provides microscopic insights into the adsorption of hazardous ions by 3DGPLs under usage conditions, but also offers a feasible approach to prevent the leakage of loaded ions through GP coating technology.
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