An emerging challenge occurs for recovering ionic liquids (ILs) because of their exponential growth in academic and industrial applications. We report for the first time to reclaim water-soluble ILs from their aqueous solutions by osmotically driving water to spontaneously permeate through semi-permeable membranes. Theoretical simulation indicates a weak hydrability of ILs and a tendency to form micelles in water. We thus demonstrate a significant difference in osmotic pressures between the aqueous solutions of ILs and inorganic salts. Four categories of broadly representative ILs are continuously recovered from their diluent aqueous solutions (~1 wt %) with semi-permeable membranes. Eventually, a record-high concentration up to 58–78 wt % is achieved in this work. Our strategy integrates superiorities of low energy consumption, universal applicability toward ILs, diversified selection of semi-permeable membranes, almost unattenuated water flux and high rejection to ions, hopefully providing new insights into the authentic “green” industrial applications of ILs.
Yu Yafeng,Pan Yi,Shen Yanting,Tian Jingxuan,Zhang Ruotong,Guo Wei,Li Chang,Shum Ho Cheung
In vascular networks, the transport across different vessel walls regulates chemical compositions in blood over space and time. Replicating such trans-wall transport with spatial heterogeneity can empower synthetic fluidic systems to program fluid compositions spatiotemporally. However, it remains challenging as existing synthetic channel walls are typically impermeable or composed of homogeneous materials without functional heterogeneity. This work presents a vascular network-inspired fluidic system (VasFluidics), which is functionalizable for spatially different trans-wall transport. Facilitated by embedded three-dimensional (3D) printing, elastic, ultrathin, and semipermeable walls self-assemble electrostatically. Physicochemical reactions between fluids and walls are localized to vary the trans-wall molecules among separate regions, for instance, by confining solutions or locally immobilizing enzymes on the outside of channels. Therefore, fluid compositions can be regulated spatiotemporally, for example, to mimic blood changes during glucose absorption and metabolism. Our VasFluidics expands opportunities to replicate biofluid processing in nature, providing an alternative to traditional fluidics.