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THE PHASE TRANSPORT AND REACTIONS OF γ-IRRADIATED AQUEOUS-IONIC LIQUIDS

机译:γ辐照水离子液体的相输运和反应

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A novel technology based on the transfer of chemical species across water/ionic liquid interfaces via specific complexation reactions is currently being considered for the separation and sequestration of metal ion contaminants from radioactive waste effluents in the nuclear fuel cycle. An ideal solvent for these applications should have a high intrinsic selectivity for a targeted metal or group of metals (e.g., trans-Pu actinides, lanthanides, or other fission products), an efficient switching mechanism (between complexation and decomplexation), and a high immiscibility with aqueous solutions. These characteristics must be maintained in the chemical, radiation, and mass transport environments present during the separation process. Ionic liquids (ILs) have an almost negligible vapour pressure and high thermal stability. Their ability to dissolve a wide range of substrate molecules and potential to be highly resilient in radiation fields make ILs particularly promising media. The separation efficiency of the biphasic system will depend on many parameters, including the aqueous oxidation state of the targeted metal ion, and the thermodynamics and kinetics of interfacial transport and metal-ligand complex formation at the water/IL interface or in the IL phase. The most uncertain and unstudied area for these applications is the effect of ionizing radiation on the stability and separation efficiency of the biphasic system. The present study investigates the effect of γ-radiation on gas/IL and water/IL interfacial stability and mass transfer with trihexyltetradecylphosphonium bis(trifluoromethyl-sulfonyl)imide, a phosphonium-based IL. The IL, in contact with either gas or water, was irradiated at a dose rate of 6.4 kGy·h~(-1). Gas-phase samples were analyzed by gas chromatography-mass spectrometry (GC-MS) and the changes in the IL and aqueous phases were monitored by conductivity measurements and Raman spectroscopy. In this paper we discuss these observations and their potential implications for nuclear waste stream separation processes.
机译:目前考虑了一种基于水/离子液体界面在水/离子液体界面转移的新型技术,用于分离和依赖于核燃料循环中的放射性废物污染物的金属离子污染物的分离和螯合。用于这些应用的理想溶剂应具有高固体选择性对靶标金属或金属组(例如,Trans-Pu散曲线,镧系元素或其他裂变产物),一种有效的开关机制(络合和解用之间),以及高效与水溶液不混溶。这些特性必须保持在分离过程中存在的化学,辐射和质量运输环境中。离子液体(ILS)具有几乎可忽略的蒸气压和高热稳定性。它们在辐射场中溶解各种衬底分子的能力和潜力是高度弹性的,使ILS特别有前途的介质。双相系统的分离效率将取决于许多参数,包括靶向金属离子的含水氧化状态,以及在水/ IL界面或IL相的界面运输和金属 - 配体复合物的热力学和动力学。这些应用的最不确定和不含糊的区域是电离辐射对双相系统的稳定性和分离效率的影响。本研究研究了γ-辐射对气体/ IL和水/ IL界面稳定性的影响,与三氧基二亚膦鏻双(三氟甲基 - 磺酰基)酰亚胺,基于鏻的IL。以6.4kGy·H〜(-1)的剂量率照射IL与一种气体或水接触。通过气相色谱 - 质谱(GC-MS)分析气相样品,通过电导测量和拉曼光谱监测IL和水相的变化。在本文中,我们讨论了这些观察结果及其对核废料流分离过程的潜在影响。

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