Lemoine Charly, Petit Yann, Karaman Thomas, Jahrsengene Gøril, Martinez Ana Maria, Benayad Anass, Billy Emmanuel
Université Grenoble Alpes, CEA, LITEN 38000 Grenoble France
SINTEF 7034 Trondheim Norway.
RSC Adv. 2024 Sep 19;14(40):29174-29183. doi: 10.1039/d4ra05135a. eCollection 2024 Sep 12.
Reducing the number of stages, energy costs and carbon footprint of recycling processes is essential to overcome environmental challenges. The interest in replacing the acids used in traditional hydrometallurgical methods with deep eutectic solvents (DES), which are less toxic and more environmentally friendly, has been growing. The aim of this study is to estimate the potential use of this class of solvents in an ionometallurgical process of leaching and electrodeposition to recover silver as part of the recycling of solar panels, a major challenge of the years to come. In the present work, a circular recycling concept based on an iron redox shuttle was studied to leach and recover silver electrodeposition. Different DESs were evaluated in combination with a hexahydrated iron(iii) chloride oxidizing agent. Ethaline DES has gained significant interest as it can attain a high silver leaching efficiency of 99.9% on crystallized silicon cell scraps at 75 °C. The promising results led to a comprehensive study of limits of this chemical system, focusing on the relation between the concentration of species (iron and water), the interfacial potential of silver (electrochemical measurements), and surface evolution (X-ray photoelectron spectroscopy analysis). Silver leaching was determined as a mixed control mechanism involving chemical and species diffusion dependence. The concentration of iron(iii) chloride appeared crucial, determining the kinetic of formation of a poorly soluble AgCl layer. Electrodeposition from leachate highlighted the need to use an oxygen-free atmosphere to produce high-quality silver. Finally, leaching at 75 °C and electrodeposition at 50 °C of silver from crystallized silicon cell scraps were demonstrated using Ethaline (1 : 2) + FeCl·6HO (0.12 mol L) under an argon atmosphere.
减少回收过程的步骤数量、能源成本和碳足迹对于克服环境挑战至关重要。用毒性较小且更环保的深共熔溶剂(DES)替代传统湿法冶金方法中使用的酸的兴趣与日俱增。本研究的目的是评估这类溶剂在浸出和电沉积的离子冶金过程中的潜在用途,以回收银,这是未来几年的一项重大挑战,是太阳能电池板回收利用的一部分。在当前工作中,研究了基于铁氧化还原穿梭的循环回收概念,用于浸出和回收银的电沉积。将不同的DES与六水合氯化铁(iii)氧化剂结合进行了评估。乙aline DES引起了广泛关注,因为在75°C下,它对结晶硅电池废料的银浸出效率可达到99.9%。这些有前景的结果促使对该化学体系的局限性进行全面研究,重点关注物种(铁和水)浓度、银的界面电位(电化学测量)和表面演变(X射线光电子能谱分析)之间的关系。银浸出被确定为一种涉及化学和物种扩散依赖性的混合控制机制。氯化铁(iii)的浓度显得至关重要,它决定了难溶性氯化银层形成的动力学。从浸出液中进行电沉积突出了需要使用无氧气氛来生产高质量银的必要性。最后,在氩气气氛下,使用乙aline(1∶2)+ FeCl·6HO(0.12 mol L)证明了在75°C下对结晶硅电池废料中的银进行浸出以及在50°C下进行电沉积。