4.8 Article

Polymeric Microcapsules as Robust Mimics of Emulsion Liquid Membranes for Selective Ion Separations

Journal

ENVIRONMENTAL SCIENCE & TECHNOLOGY
Volume 56, Issue 23, Pages 17352-17363

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.est.2c07242

Keywords

selective ion separations; facilitated transport membranes; resource recovery; wastewater treatment; hydrometallurgy; microcapsules; extraction

Funding

  1. U.S. Department of Energy (BES Award) [RGPIN-2021-02729]
  2. Natural Sciences and Engineering Research Council of Canada
  3. NSF through the MRSEC program
  4. [DE-SC0020210]

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Selective ion separations are crucial for addressing water scarcity, resource recovery from wastewater, and electronics waste recycling. This study demonstrates that polymeric microcapsules can serve as stable and solvent-free alternatives to emulsion liquid membranes, enabling efficient ion separations.
Selective ion separations are increasingly needed to combat water scarcity, recover resources from wastewater, and enable the efficient recycling of electronics waste. Emulsion liquid membranes (ELMs) have received interest due to rapid kinetics, high selectivities, and low solvent requirements but are too unstable for industrial usage. We demonstrate that polymeric microcapsules can serve as robust, solvent-free mimics of ELMs. As a proof of concept, we incorporated the copper-selective ligand Lix 84-I in the walls of microcapsules formed from a commercial polystyrene-b-polybutadiene-b- polystyrene triblock polymer. The microcapsules were formed from a double-emulsion template, resulting in particles typically 20-120 mu m in diameter that encapsulated even smaller droplets of a dilute (<= 0.5 M) H2SO4 solution. Batch experiments demonstrated facilitated-transport behavior, with equilibrium reached in as little as 10 min for microcapsules with 1% ligand, and with similar to 15-fold selectivity for Cu2+ over Ni2+. Furthermore, the microcapsules could be packed readily in columns for flow-through operation, thus enabling near-complete Cu2+ removal in similar to 2 min under certain conditions, recovery of Cu2+ by flowing through fresh dilute H2SO4, and reuse for at least 10 cycles. The approach in this work can serve as a template for using selective ligands to enable robust and simple flow-through processes for a variety of selective ion separations.

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