We fabricated a thin-film composite (TFC) forward osmosis (FO) membrane with an ultrathin spray-coated carbon nanotube (CNT) interlayer. The impact of the CNT interlayer on the polyamide (PA) layer structural properties and transport behavior in FO were investigated. Results indicate that the CNT interlayer provides an interface which enables the formation of a highly permeable and selective PA layer with a large effective surface area for water transport, while inhibiting the formation of a flowerlike PA structure inside the substrate pores. The TFC-FO membrane with the CNT interlayer exhibited a much greater water flux than previously reported for FO membranes, while maintaining comparable salt rejection. Specifically, a membrane perm-selectivity or ratio of water (A) to salt permeability coefficients (B) (A/B value) of 39 bar −1 was achieved for the TFC-PA-CNT membrane. Implications of the results for the fabrication of highperformance TFC-FO membranes are further discussed.
A triple-layered TFC nanofiltration (NF) membrane consisting of a polyamide (PA) top layer covered on a poly(ether sulfone) microfiltration membrane with a carbon nanotube (CNT) interlayer was fabricated via interfacial polymerization. The structure and properties of the PA active layer could be finely tailored by tuning the interfacial properties and pore structure of the CNT interlayer, including its surface pore size and thickness, thus improving its NF performance. This TFC NF membrane exhibited a high divalent salt rejection (the rejection of Na 2 SO 4 and MgSO 4 solution >98.3%) and dye rejection (the rejection of methyl violet (MV) >99.5%) with a high pure water flux of around 21 L m −2 h −1 bar −1 . Excitingly, this membrane also showed excellent selectivity to both mono/divalent salt ion (the selectivity of Cl − /SO 4 2− is as high as 85.5) and NaCl/dye solution (the selectivity of NaCl/MV is more than 123.5), which are much higher than most of other commercial and reported NF membranes. Moreover, this membrane also showed a good separation performance and long-term stability during a continuous NF process for a salt/dye mixture solution. This triple-layered TFC NF membrane showed a great promise for applications in both wastewater treatment and dyes recycling.
Nanofluidic membranes have been demonstrated
as promising candidates
for osmotic energy harvesting. However, it remains a long-standing
challenge to fabricate high-efficiency ion-permselective membranes
with well-defined channel architectures. Here, we demonstrate high-performance
osmotic energy conversion membranes based on oriented two-dimensional
covalent organic frameworks (COFs) with ultrashort vertically aligned
nanofluidic channels that enabled efficient and selective ion transport.
Experiments combined with molecular dynamics simulations revealed
that exquisite control over channel orientation, charge polarity,
and charge density contributed to high ion selectivity and permeability.
When applied to osmotic energy conversion, a pair of 100 nm thick
oppositely charged COF membranes achieved an ultrahigh output power
density of 43.2 W m–2 at a 50-fold salinity gradient
and up to 228.9 W m–2 for the Dead Sea and river
water system. The achieved power density outperforms the state-of-the-art
nanofluidic membranes, suggesting the great potential of oriented
COF membranes in the fields of advanced membrane technology and energy
conversion.
Pore size uniformity is one of the most critical parameters in determining membrane separation performance. Recently, a novel type of conjugated microporous polymers (CMPs) has shown uniform pore size and high porosity. However, their brittle nature has prevented them from preparing robust membranes. Inspired by the skin-core architecture of spider silk that offers both high strength and high ductility, herein we report an electropolymerization process to prepare a CMP membrane from a rigid carbazole monomer, 2,2’,7,7’-tetra(carbazol-9-yl)-9,9’-spirobifluorene, inside a robust carbon nanotube scaffold. The obtained membranes showed superior mechanical strength and ductility, high surface area, and uniform pore size of approximately 1 nm. The superfast solvent transport and excellent molecular sieving well surpass the performance of most reported polymer membranes. Our method makes it possible to use rigid CMPs membranes in pressure-driven membrane processes, providing potential applications for this important category of polymer materials.
Polymer membranes typically possess a broad pore-size distribution that leads to much lower selectivity in ion separation when compared to membranes made of crystalline porous materials; however, they are highly desirable because of their easy processability and low cost. Herein, we demonstrate the fabrication of ionsieving membranes based on a polycarbazole-type conjugated microporous polymer using an easy to scale-up electropolymerization strategy. The membranes exhibited high uniform sub-nanometer pores and a precisely tunable membrane thickness, yielding a high ion-sieving performance with a sub-1 Å size precision. Both experimental results and molecular simulations suggested that the impressive ionsieving performance of the CMP membranes originates from their uniform and narrow pore-size distribution.
Nanofluidic ion transport holds high promise in bio‐sensing and energy conversion applications. However, smart nanofluidic devices with high ion flux and modulable ion transport capabilities remain to be realised. Herein, we demonstrate smart nanofluidic devices based on oriented two‐dimensional covalent organic framework (2D COF) membranes with vertically aligned nanochannel arrays that achieved a 2–3 orders of magnitude higher ion flux compared with that of conventional single‐channel nanofluidic devices. The surface‐charge‐governed ion conductance is dominant for electrolyte concentration up to 0.01 M. Moreover, owing to the customisable pH‐responsivity of imine and phenol hydroxyl groups, the COF‐DT membranes attained an actively modulable ion transport with a high pH‐gating on/off ratio of ≈100. The customisable structure and rich chemistry of COF materials will offer a promising platform for manufacturing nanofluidic devices with modifiable ion/molecular transport features.
A green and sustainable technique is desired for juice concentration to increase its shelf life and save the transportation cost. In this study, we investigated an integrated forward osmosis-membrane distillation (FO-MD) process for juice concentration and developed a food preservative potassium sorbate as a renewable draw solute. The upstream FO process was used to concentrate apple juice in ambient operation conditions for preserving juice nutrition and flavor. Potassium sorbate preservative was developed as draw solute to minimize the accumulation of a draw solute in the concentrated juice without interfering juice flavor, and the slow diffusion of potassium sorbate preservative across the FO membrane to the feed juice concentrate can also prevent the bacterial growth during the concentration process by taking advantage of reverse salt flux. The downstream MD process was used to recover potassium sorbate draw solutes from the FO effluent and maintain the constant draw solute concentration for achieving stable water flux of FO membranes. Thin-film composite (TFC) polyamide membranes and poly (vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) electrospun nanofibrous membranes were fabricated and employed in the FO and MD processes, respectively. Results illustrate that the integrated FO-MD process presents a synergistic flux balancing behavior and achieves a constant water flux for both FO and MD membranes. The FO-MD process was able to continuously concentrate apple juice over longterm bench-scale operation. Importantly, the concentrated apple juice has almost no loss in nutrition and also has very low amount of potassium sorbate (0.45 g/L) far below the required maximum level in food industry (1.00 g/L). Our work provides a food preservative potassium sorbate draw solute facilitated FO-MD process for juice concentration, which may have practical application potentials in the food processing.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.