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基于柠檬酸构建的深共晶溶剂基双水相体系在绿色金分离中的优异性能。

Outstanding Performance of the Deep Eutectic Solvent-Based Aqueous Biphasic System Constructed with Sodium Citrate for a Green Gold Separation.

机构信息

Research Center of Lake Restoration Technology Engineering for Universities of Yunnan Province, School of Chemical Science and Technology, Yunnan University, Kunming, Yunnan 650091, China.

出版信息

Langmuir. 2023 Jul 11;39(27):9538-9550. doi: 10.1021/acs.langmuir.3c01076. Epub 2023 Jun 27.

DOI:10.1021/acs.langmuir.3c01076
PMID:37366178
Abstract

Aqueous biphasic systems (ABSs) that are based on deep eutectic solvents (DESs) are environmentally benign systems to use for metal ion separation. In this work, a series of DESs was synthesized for the first time with PEG 400 as hydrogen bond donors and tetrabutylphonium bromide (PBr), tetrabutylammonium bromide (NBr), or tetrabutylammonium chloride (NCl) as hydrogen bond acceptors, and then they were combined with citrate (NaCHO), which is eco-friendly, to construct an ABS for use in the separation of Au(I) from an aurocyanide solution. Phase diagrams of DESs + NaCHO + HO systems were constructed using the experimentally measured data. Multiple factors that affect the efficiency of the gold extraction were studied; these factors were the species of salt or DES and their content, the equilibrium pH, the oscillation time, and the initial gold concentration. Gold(I) is preferentially retained in the DES-rich phase, and the PBr:PEG 1:2 + NaCHO + HO system has a high extraction efficiency of 100.0% under optimized conditions. FT-IR, NMR, and TEM characterizations and DFT calculations show that the migration of Au(I) from the salt-rich to the DES-rich phase follows an ion exchange mechanism. Specifically, Au(CN) replaces Br in the original PBr and generates a stable ion pair with the quaternary phosphonium salt cation, P, and this replacement is driven by electrostatic attractions. A new strong hydrogen bond network simultaneously forms between the anionic Au(CN) and the -OH group in the PEG 400 component. Finally, the gold of Au(I)-loaded PBr:PEG 1:2 can be successfully reduced by sodium borohydride with an efficiency of 100.0%. The strategy to extract gold(I) from alkaline cyanide solutions using an ABS based on DESs as proposed in this work provides a potential platform for developing green technology for recovering gold.

摘要

基于离子液体的双水相体系用于金属离子分离的环境友好体系。在这项工作中,首次合成了一系列以 PEG 400 为氢键供体、四丁基溴化磷(PBr)、四丁基溴化铵(NBr)或四丁基氯化铵(NCl)为氢键受体的 DES,并与环保的柠檬酸钠(NaCHO)结合,构建了用于从金氰络合物溶液中分离 Au(I) 的双水相体系。使用实验测量数据构建了 DES+NaCHO+HO 体系的相图。研究了影响金萃取效率的多种因素,包括盐或 DES 的种类及其含量、平衡 pH 值、振荡时间和初始金浓度。Au(I)优先保留在 DES 富相,在优化条件下,PBr:PEG 1:2+NaCHO+HO 体系的萃取效率高达 100.0%。FT-IR、NMR、TEM 表征和 DFT 计算表明,Au(I)从盐富相迁移到 DES 富相遵循离子交换机制。具体而言,Au(CN)取代原始 PBr 中的 Br,并与季膦盐阳离子 P 生成稳定的离子对,这种取代是由静电吸引力驱动的。同时,阴离子 Au(CN)与 PEG 400 组分中的-OH 基团之间形成新的强氢键网络。最后,Au(I)负载的 PBr:PEG 1:2 中的金可以被硼氢化钠成功还原,效率为 100.0%。本工作提出的基于 DES 的双水相体系从碱性氰化物溶液中提取 Au(I)的策略为开发回收金的绿色技术提供了一个潜在的平台。

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