Thin continuous membrane coating with high surface energy for comprehensive antifouling seawater distillation.

Membrane distillation (MD) has prominent advantages such as treating high-salinity wastewater with a low-grade thermal energy, high salt rejection, and zero discharge. However, organic fouling and mineral scaling are two major challenges for hydrophobic MD membranes when used for practical applications. Commonly, improving organic fouling- and mineral scaling-resistance require oppositely enhanced wetting properties of membrane, thus is difficult to simultaneously realize dual resistance with one membrane. Here, we proposed to use underwater thermodynamically stable high-surface-energy coating to modify the hydrophobic membrane with Janus structures comprising different surface energy. The underlayered structure meets the hydrophobicity requirements of the MD membrane, while the coating layer realizes dual resistance to organic and inorganic foulants. Theoretical analysis and experimental proof reveal that the membrane with the high-surface-energy coating layer outperforms the pristine one with approximately 10 times of longevity. This strategy provides a new way for the use of high-surface-energy materials in versatilely fouling-resistant MD process.

Deformation constraints of graphene oxide nanochannels under reverse osmosis.

Nanochannels in laminated graphene oxide nanosheets featuring confined mass transport have attracted interest in multiple research fields. The use of nanochannels for reverse osmosis is a prospect for developing next-generation synthetic water-treatment membranes. The robustness of nanochannels under high-pressure conditions is vital for effectively separating water and ions with sub-nanometer precision. Although several strategies have been developed to address this issue, the inconsistent response of nanochannels to external conditions used in membrane processes has rarely been investigated. In this study, we develop a robust interlayer channel by balancing the associated chemistry and confinement stability to exclude salt solutes. We build a series of membrane nanochannels with similar physical dimensions but different channel functionalities and reveal their divergent deformation behaviors under different conditions. The deformation constraint effectively endows the nanochannel with rapid deformation recovery and excellent ion exclusion performance under variable pressure conditions. This study can help understand the deformation behavior of two-dimensional nanochannels in pressure-driven membrane processes and develop strategies for the corresponding deformation constraints regarding the pore wall and interior.

Unveiling the impact of imidazole derivative with mechanistic insights into neutralize interfacial polymerized membranes for improved solute-solute selectivity.

Domestic wastewater (DWW) contains a reservoir of nutrients, such as nitrogen, potassium, and phosphorus; however, emerging micropollutants (EMPs) hinder its applications in resource recovery. In this study, a novel class of nanofiltration (NF) membranes was developed; it enabled the efficient removal of harmful EMP constituents while preserving valuable nutrients in the permeate. Neutral (IM-N) and positively charged (IM-P) imidazole derivative compounds have been used to chemically functionalize pristine polyamide (PA) membranes to synchronously inhibit the hydrolysis of residual acyl chloride and promote their amination. Owing to their distinct properties, these IM modifiers can custom-build the membrane physicochemical properties and structures to benefit the NF process in DWW treatment. The electroneutral NF membrane exhibited ultrahigh solute-solute selectivity by minimizing the Donnan effects on ion penetration (K, N, and P ions rejection < 25%) while imposing remarkable size-sieving obstruction against EMPs (rejection ratio > 91%). Moreover, the hydrophilic IM-modifier synergistically led to enhanced water permeance of 9.2 L m-2 h-1 bar-1, reaching a 2-fold higher magnitude than that of the pristine PA membrane, along with excellent antifouling/antibacterial fouling properties. This study may provide a paradigm shift in membrane technology to convert wastewater streams into valuable water and nutrient resources.

Chemically Converted Graphene Nanosheets for the Construction of Ion-Exclusion Nanochannel Membranes.

Water and ion transport in nanochannels is an intriguing topic that has been extensively investigated in several energy- and environment-related research fields. Recently developed two-dimensional (2D) materials are ideal building blocks for constructing confined nanochannels by self-stacking. Among these, graphene oxide (GO) is the most frequently employed as the starting material because of its excellent solution processability. Since solvation of the GO nanostructure usually impairs the function of nanochannels, in this study, chemically converted graphene was prepared using a one-step method, to simultaneously acquire the desired stability and functionality of the nanochannels. The confined channels with high charge densities are capable of excluding ∼90% NaCl solutes from water in a pressure-driven filtration process. This surpasses the performance of most GO desalination membranes reported in the literature. Thus, this study provides useful information for the feasible development of ion-exclusion nanochannel membranes based on the proposed nanochannel-confined charge repulsion mechanism.

Engineering Heterostructured Thin-Film Nanocomposite Membrane with Functionalized Graphene Oxide Quantum Dots (GOQD) for Highly Efficient Reverse Osmosis.

In this study, custom-tailored graphene oxide quantum dots (GOQD) were synthesized as functional nanofillers to be embedded into the polyamide (PA) membrane for reverse osmosis (RO) via interfacial polymerization (IP). The heterostructured interface-functionalization of amine/sulfonic decoration on GOQD (N/S-d-GOQD) takes place via the tuning of the molecular design. The embedded N/S-d-GOQD inside the PA matrix contributes to facilitating water molecules quick transport due to the more accessible capturing sites with higher internal polarity, achieving a nearly 3-fold increase in water permeance when compared to the pristine thin-film composite (TFC) membrane. Covalent bonding between the terminal amine groups and the acyl chloride of trimesoyl chloride (TMC) enables the formation of an amplified selective layer, while the sulfonic part assists in maintaining a robust membrane surface negative charge, thus remarkably improving the membrane selectivity toward NaCl. As a result, the newly developed TFN membrane performed remarkably high water permeance up to 5.89 L m-2 h-1 bar-1 without the compromising of its favorable salt (NaCl) rejection ratio of 97.1%, revealing a comparably high separation property when comparing to the state-of-the-art RO membranes, and surpassing the permeability-selectivity trade-off limits. Furthermore, we systematically investigated the GOQDs with different surface decorations but similar configurations (including 3 different nanofillers of pristine GOQD, amine decorated GOQD (N-d-GOQD), and N/S-d-GOQD) to unveil the underlying mechanisms of the swing effects of internal geometry and polarity of the embedded nanofillers on contributing to the uptake, and/or release of aqueous molecules within TFN membranes, providing a fundamental perspective to investigate the impact of embedded nanofillers on the formation of an IP layer and the overall transporting behavior of the RO process.

Improved Performance of Polysulfone Ultrafiltration Membrane Using TCPP by Post-Modification Method.

Ultrafiltration (UF) membranes have found great application in sewage purification and desalination due to their high permeation flux and high rejection rate for contaminants under low-pressure conditions, but the flux and antifouling ability of UF membranes needs to be improved. Tetrakis (4-carboxyphenyl) porphyrin (TCPP) has good hydrophilicity, and it is protonated under strongly acidic conditions and then forms strong hydrogen bonds with N, O and S, so that the TCPP would be well anchored in the membrane. In this work, NaHCO3 was used to dissolve TCPP and TMC (trimesoyl chloride) was used to produce a strong acid. Then, TCPP was modified in a membrane with a different rejection rate by a method similar to interfacial polymerization. Performance tests of TCPP/polysulfone (PSf) membranes show that for the membrane with a high BSA (bovine serum albumin) rejection, when the ratio of NaHCO3 to TCPP is 16:1 (wt.%), the pure water flux of membrane Z1 16:1 is increased by 34% (from 455 to 614 Lm-2h-1bar-1) while the membrane retention was maintained above 95%. As for the membrane with a low BSA rejection, when the ratio of NaHCO3 to TCPP was 32:1, the rejection of membrane B2 32:1 was found to increase from 81% to 96%. Although the flux of membrane B2 32:1 decreased, it remained at 638 Lm-2h-1bar-1, which is comparable to the reported polymer ultrafiltration membrane. The above dual results are thought to be attributed to the synergistic effect of protonated TCPP and NaHCO3, where the former increases membrane flux and the latter increases the membrane rejection rate. This work provides a way for the application of porphyrin and porphyrin framework materials in membrane separation.