4.8 Article

Modification of Cation-Exchange Membranes with Polyelectrolyte Multilayers to Tune Ion Selectivity in Capacitive Deionization

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 12, 期 31, 页码 34746-34754

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.0c05664

关键词

mono/divalent cation selectivity; polyelectrolyte multilayers; capacitive deionization; cation-exchange membrane; sodium removal

资金

  1. European Research Council (ERC Consolidator Grant) [682444]
  2. European Research Council (ERC) [682444] Funding Source: European Research Council (ERC)

向作者/读者索取更多资源

Capacitive deionization (CDI) is a desalination technique that can be applied for the separation of target ions from water streams. For instance, mono- and divalent cation selectivities were studied by other research groups in the context of water softening. Another focus is on removing Na+ from recirculated irrigation water (IW) in greenhouses, aiming to maintain nutrients. This is important as an excess of Na+ has toxic effects on plant growth by decreasing the uptake of other nutrients. In this study, we investigated the selective separation of sodium (Na+) and magnesium (Mg2+) in MCDI using a polyelectrolyte multilayer (PEM) on a standard grade cation-exchange membrane (Neosepta, CMX). Alternating layers of poly(allylamine hydrochloride) (PAH) and poly(styrene sulfonate) (PSS) were coated on a CMX membrane (CMX-PEM) using the layer-by-layer (LbL) technique. The layer formation was examined with X-ray photoelectron spectroscopy (XPS) and static water contact angle measurements (SWA) for each layer. For each membrane, i.e., the CMX-PEM membrane, CMX membrane, and for a special-grade cation-exchange membrane (Neosepta, CIMS), the Na+/Mg2+ selectivity was investigated by performing MCDI experiments, and selectivity values of 2.8 +/- 0.2, 0.5 +/- 0.04, and 0.4 +/- 0.1 were found, respectively, over up to 40 cycles. These selectivity values indicate flexible switching from a Met-selective membrane to a Nat-selective membrane by straightforward modification with a PEM. We anticipate that our modular functionalization method may facilitate the further development of ion-selective membranes and electrodes.

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