Shen Yu-Yi, Wu Shan-Wen, Hou Chia-Hung
Graduate Institute of Environmental Engineering, National Taiwan University, No. 1, Sec. 4. Roosevelt Rd., Taipei 10617, Taiwan.
Graduate Institute of Environmental Engineering, National Taiwan University, No. 1, Sec. 4. Roosevelt Rd., Taipei 10617, Taiwan; Water Innovation, Low Carbon and Environmental Sustainability Research Center, National Taiwan University, Taipei 10617, Taiwan.
J Colloid Interface Sci. 2021 Mar 15;586:819-829. doi: 10.1016/j.jcis.2020.11.006. Epub 2020 Nov 5.
High-efficiency recycling technology for endangered elements effectively mitigates the risk of resource shortages and promises the sustainability of supply chains, which is significant to the industry. In this study, an activated carbon (AC)-based capacitive deionization (CDI) for the selective electrosorption and recovery of indium ions (In) from acidic aqueous solution is proposed. The effects of applied voltage, pH, and initial concentration of indium were investigated to optimize the operation parameters for In electrosorption. The results of cyclic voltammetry and the galvanostatic charge/discharge measurements indicate that the AC electrode shows good capability for the electrosorption of In based on electrical double-layer capacitance. As demonstrated, In can be successfully removed by CDI without deposition when the pH < 4, as confirmed by scanning electron microscopy and energy dispersive X-ray spectroscopy. The deionization capacity of In is 7.95 mg/g with an energy consumption of 0.84 kWh/mol in single-pass mode CDI with an initial concentration of 50 mg/L (pH = 3) at 1.2 V. However, the removal of In is affected by the solution pH since hydrogen ions (H) compete for electrosorption. Note that In ions with high valence are preferentially electrosorbed on the electrode surface over H ions, exhibiting a selectivity coefficient of 2.12. Herein, in the charging step, a large number of H ions in solution are rapidly electrosorbed onto the electrode, while these H ions are gradually replaced by a small number of In ions in solution. Therefore, this electrosorption process shows great potential for effectively recovering indium ions from acidic aqueous solutions.
濒危元素的高效回收技术有效降低了资源短缺风险,并保证了供应链的可持续性,这对该行业具有重要意义。在本研究中,提出了一种基于活性炭(AC)的电容去离子化(CDI)方法,用于从酸性水溶液中选择性电吸附和回收铟离子(In)。研究了施加电压、pH值和铟的初始浓度对铟电吸附操作参数的影响,以进行优化。循环伏安法和恒电流充放电测量结果表明,基于双电层电容,AC电极对铟的电吸附具有良好的能力。扫描电子显微镜和能量色散X射线光谱证实,当pH < 4时,铟可以通过CDI成功去除而不发生沉积。在1.2 V下,初始浓度为50 mg/L(pH = 3)的单通道模式CDI中,铟的去离子化容量为7.95 mg/g,能耗为0.84 kWh/mol。然而,由于氢离子(H)竞争电吸附,铟的去除受到溶液pH值的影响。需要注意的是,高价铟离子比H离子更优先电吸附在电极表面,选择性系数为2.12。在此,在充电步骤中,溶液中的大量H离子迅速电吸附到电极上,而这些H离子逐渐被溶液中的少量铟离子取代。因此,这种电吸附过程在从酸性水溶液中有效回收铟离子方面显示出巨大潜力。