Browsing by Author "Walker, W. Shane"
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Item Aqueous-Processed, High-Capacity Electrodes for Membrane Capacitive Deionization(American Chemical Society, 2018) Jain, Amit; Kim, Jun; Owoseni, Oluwaseye M.; Weathers, Cierra; Caña, Daniel; Zuo, Kuichang; Walker, W. Shane; Li, Qilin; Verduzco, Rafael; NSF Nanosystems Engineering Research Center, Nanotechnology-Enabled Water TreatmentMembrane capacitive deionization (MCDI) is a low-cost technology for desalination. Typically, MCDI electrodes are fabricated using a slurry of nanoparticles in an organic solvent along with polyvinylidene fluoride (PVDF) polymeric binder. Recent studies of the environmental impact of CDI have pointed to the organic solvents used in the fabrication of CDI electrodes as key contributors to the overall environmental impact of the technology. Here, we report a scalable, aqueous processing approach to prepare MCDI electrodes using water-soluble polymer poly(vinyl alcohol) (PVA) as a binder and ion-exchange polymer. Electrodes are prepared by depositing aqueous slurry of activated carbon and PVA binder followed by coating with a thin layer of PVA-based cation- or anion-exchange polymer. When coated with ion-exchange layers, the PVA-bound electrodes exhibit salt adsorption capacities up to 14.4 mg/g and charge efficiencies up to 86.3%, higher than typically achieved for activated carbon electrodes with a hydrophobic polymer binder and ion-exchange membranes (5–13 mg/g). Furthermore, when paired with low-resistance commercial ion-exchange membranes, salt adsorption capacities exceed 18 mg/g. Our overall approach demonstrates a simple, environmentally friendly, cost-effective, and scalable method for the fabrication of high-capacity MCDI electrodes.Item Selective membranes in water and wastewater treatment: Role of advanced materials(Elsevier, 2021) Zuo, Kuichang; Wang, Kunpeng; DuChanois, Ryan M.; Fang, Qiyi; Deemer, Eva M.; Huang, Xiaochuan; Xin, Ruikun; Said, Ibrahim A.; He, Ze; Feng, Yuren; Walker, W. Shane; Lou, Jun; Elimelech, Menachem; Huang, Xia; Li, Qilin; NSF Nanosystems Engineering Research Center for Nanotechnology-Enabled Water TreatmentMembrane separation has enjoyed tremendous advances in relevant material and engineering sciences, making it the fastest growing technology in water treatment. Although membranes as a broad-spectrum physical barrier have great advantages over conventional treatment processes in a myriad of applications, the need for higher selectivity and specificity in membrane separation is rising as we move to target contaminants at trace concentrations and to recover valuable chemicals from wastewater with low energy consumption. In this review, we discuss the drivers, fundamental science, and potential enabling materials for high selectivity membranes, as well as their applications in different water treatment processes. Membrane materials and processes that show promise to achieve high selectivity for water, ions, and small molecules—as well as the mechanisms involved—are highlighted. We further identify practical needs, knowledge gaps, and technological barriers in both material development and process design for high selectivity membrane processes. Finally, we discuss research priorities in the context of existing and future water supply paradigms.Item Self assembled, sulfonated pentablock copolymer cation exchange coatings for membrane capacitive deionization(Royal Society of Chemistry, 2019) Jain, Amit; Weathers, Cierra; Kim, Jun; Meyer, Matthew D.; Walker, W. Shane; Li, Qilin; Verduzco, Rafael; Nanosystems Engineering Research Center for Nanotechnology-Enabled Water TreatmentMembrane capacitive deionization (MCDI) is a simple and low-cost method for brackish water desalination involving reversible electrosorption using high surface area, porous electrodes paired with ion-exchange membranes. Ion-exchange membranes improve charge efficiency and salt adsorption capacity by limiting the transport of co-ions and inhibiting faradaic reactions at the electrode surface. Effective ion-exchange membranes for MCDI should have high permselectivity and low ionic resistance, but there is typically a trade-off between these two properties. In this work, we studied partially sulfonated pentablock copolymer (sPBC) as a cation-exchange coating for MCDI electrodes. sPBC ion exchange coatings of varying ion exchange capacity (IEC, 1.0, 1.5, 2.0 meq g−1) and a range of casting solvent compositions (10–60 wt% n-propanol in toluene) were prepared. Transmission electron microscopy analysis of the membranes showed a morphological change from a micellar to lamellar and then to an inverse micellar structure with increasing polarity of the casting solvent. Water uptake and salt permeability increased with increasing IEC and casting solvent polarity over the entire range of conditions tested. MCDI device studies indicated that charge efficiency and salt adsorption capacity both increased with water uptake over a range of casting solvent compositions due to morphological changes in the sPBC film. This work demonstrates an effective solution-processible ion-exchange layer for MCDI using a self-assembling block copolymer and suggests that ideal ion-exchange coatings for MCDI should have high water uptake to minimize ionic resistance while at the same time maintaining a high charge density of fixed charged groups to achieve high permselectivity.