Calogera Bertoloni, Sophie Legeai, Stéphanie Michel, Eric Meux and François Lapicque
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引用次数: 0
摘要
为了在同一电池中通过电化学浸出和沉积步骤有选择性地回收电子废弃物中的贵重成分,本研究介绍了在绿色深共晶溶剂(DES)中对银的两种反应进行的电化学研究。除了由氯化胆碱和乙二醇形成的乙碱 1 : 2 之外,还有丙碱 1 :3 的丙二醇进行了测试。根据温度和含水量测定这两种 DES 的密度、粘度和电导率,可得出 0.70 至 0.90 的离子度值,这些操作参数会产生负面影响。只要有足够的温度和低于 5 wt% 的含水量,在 1 mA cm-2 的条件下就能从这两种 DES 中萃取出纯银,法拉第产量接近 100%。在旋转电极的瞬态或稳态下,通过循环伏安法和安培计对电沉积进行了全面检测,从而得出了两种 DES 中的银(I)扩散值。此外,还根据循环伏安图估算了电沉积反应的动力学参数,并将其模拟为不可逆反应。在 60 °C 和 0.25 mA cm-2 干燥气氛下进行的长达 24 小时的测试中,产生了厚厚的银沉积物,电流效率接近 100%。沉积物由大小为 15-20 μm 的规则小颗粒凝聚而成,具有良好的附着力。
Electroleaching and electrodeposition of silver in ethaline 1 : 2 and propeline 1 : 3: transport properties and electrode phenomena†
In view of selectively recovering precious contents in electronic waste by combined electrochemical leaching and deposition step in the same cell, this study presents electrochemical investigations of the two reactions conducted in green deep eutectic solvents (DESs) for the case of silver. In addition to ethaline 1 : 2 formed from choline chloride and ethylene glycol, propeline 1 : 3 with less nocive propylene glycol was tested. Determination of the density, viscosity and conductivity of the two DES depending on temperature and their water content could lead to ionicity values from 0.70 to 0.90, with a negative effect of these operating parameters. Pure silver can be leached at 1 mA cm−2 with faradaic yield near 100% from the two DES, provided sufficient temperature and water content below 5 wt%. Electrodeposition was thoroughly examined by cyclic voltammetry and amperometry at transient or steady state at a rotating electrode, leading to Ag(I) diffusivity values in the two DES. Kinetic parameters of the electrodeposition reaction, modelled as irreversible, were also estimated from cyclic voltammograms. Thick silver deposits were produced in 24 h-long tests at 60 °C and 0.25 mA cm−2 in a dry atmosphere with nearly 100% current efficiency. The deposits were formed by little coalesced regular grains of size 15–20 μm and exhibiting fair adherence.