Crown ether containing polyelectrolyte multilayer membranes for lithium recovery

聚电解质 选择性 聚乙烯亚胺 化学 冠醚 纳滤 化学工程 乙醚 聚合物 高分子化学 无机化学 有机化学 离子 催化作用 工程类 基因 生物化学 转染
作者
Mohammad Kazemabad,Arne Verliefde,Emile Cornelissen,Arnout D’Haese
出处
期刊:Journal of Membrane Science [Elsevier BV]
卷期号:595: 117432-117432 被引量:70
标识
DOI:10.1016/j.memsci.2019.117432
摘要

Achieving solute selectivity has always been a goal of membrane development studies. The continuing growth of global consumption of scarce metals by different industries has put a strain on traditional sources of these species. Achieving cation selectivity in membranes, especially among monovalent cations, is a major step in introducing alternative sources for scarce metals such as lithium. Polyelectrolyte multilayer membranes (PEMMs) are a novel class of membranes, offering great potentials in monovalent/bivalent ion selectivity. On the other hand, crown ethers are a well-studied family of macrocyclic ligands capable of forming stable complexes with cations. In the current study, for the first time, we report on a PEMM nanofiltration membrane with crown ether moieties embedded in its structure for the goal of achieving monovalent salt selectivity. The crown ether 15-crown-5 was successfully incorporated in the polycation polyethylenimine (PEI), which was then used as the polycation in PEMM formation through layer by layer deposition. Both the synthesized polymer and the polyelectrolyte multilayer (PEM) were characterized and the performance of the resulting membrane was studied. It was determined that crown ether containing polymer forms more stable complexes with lithium than potassium. This was explained by the limitation put on 2:1 potassium-crownether complexes by steric hindrance from polymer chain. The manufactured membranes showed Li/K selectivity for a period of around 90 min, after which the crown ethers became saturated and selectivity was lost. The modified membranes became non selective after this point, but possessed high salt rejection potential.
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