College of Chemistry, Sichuan University, Key Laboratory of Radiation Physics & Technology, Ministry of Education, Chengdu 610064, PR China.
J Colloid Interface Sci. 2012 Nov 15;386(1):291-9. doi: 10.1016/j.jcis.2012.07.070. Epub 2012 Aug 2.
A new solid-phase extraction adsorbent was prepared by employing a two-step "grafting from" approach to anchor a multidentate N-donor ligand, 5-azacytosine onto hydrothermal carbon (HTC) microspheres for highly selective separation of U(VI) from multi-ion system. Fourier-transform infrared and X-ray photoelectron spectroscopies were used to analyze the chemical structure and properties of resultant HTC-based materials. The adsorption behavior of U(VI) onto the adsorbent was investigated as functions of pH, contact time, ionic strength, temperature, and initial U(VI) concentration using batch adsorption experiments. The U(VI) adsorption was of pH dependent. The adsorption achieved equilibrium within 30 min and followed a pseudo-second-order equation. The adsorption amount of U(VI) increased with raising the temperature from 283.15 to 333.15K. Remarkably, high ionic strength up to 5.0 mol L(-1) NaNO(3) had only slight effect on the adsorption. The maximum U(VI) adsorption capacity reached 408.36 mg g(-1) at 333.15K and pH 4.5. Results from batch experiments in a simulated nuclear industrial effluent, containing 13 co-existing cations including uranyl ion, showed a high adsorption capacity and selectivity of the adsorbent for uranium (0.63 mmol U g(-1), accounting for about 67% of the total adsorption amount).
一种新型固相萃取吸附剂通过两步“接枝”方法制备,即将多齿 N-供体配体 5-氮杂胞嘧啶锚定到水热碳(HTC)微球上,用于从多离子体系中高度选择性地分离 U(VI)。傅里叶变换红外和 X 射线光电子能谱用于分析所得 HTC 基材料的化学结构和性能。通过批处理吸附实验研究了 U(VI)在吸附剂上的吸附行为作为 pH、接触时间、离子强度、温度和初始 U(VI)浓度的函数。U(VI)的吸附依赖于 pH。吸附在 30 分钟内达到平衡,符合准二级方程。吸附量 U(VI)随温度从 283.15 升高到 333.15K 而增加。值得注意的是,高达 5.0 mol L(-1)的高离子强度 NaNO(3)对吸附的影响很小。在 333.15K 和 pH 4.5 下,U(VI)的最大吸附容量达到 408.36mg g(-1)。在模拟核工业废水中的批实验结果,其中含有 13 种共存阳离子,包括铀酰离子,表明该吸附剂对铀具有高吸附容量和选择性(0.63mmol U g(-1),占总吸附量的约 67%)。