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The cosolvent-assisted interfacial polymerization (CAIP) has garnered significant attention due to its capacity to easily and effectively modify the performance of polyamide (PA) reverse osmosis (RO) membranes. To gain deeper understanding of the mechanism of a specific type of cosolvents on the IP reaction, namely N,N-dimethylformamide (DMF), N,N-dimethylacetamide (DMAc), and N,N-dimethylpropionamide (DMPr) were used as aqueous-phase cosolvents to systematically investigate their effects on the membrane structures and properties under different conditions. Amide cosolvents in the aqueous phase facilitated the diffusion of the amine monomer and the formation of nanovoids within the PA layer as the C-chain length of amides increased. When 1,2-dichloroethane was also included in the organic phase, the extent of the two-phase miscible zone was further increased with its assistance, which contributed to generating the larger nanovoids within the layer, thicker PA layer and extensive exterior PA layers, as well as significantly enhancing the water permeability and selectivity of membranes. Importantly, this study successfully prepared high-performance RO membranes with multilayer nanovoid structures in situ by introducing cosolvents in the IP reaction with permeability up to 2.26 L·m−2·h−1·bar−1, providing theoretical and experimental bases for further enrichment of CAIP. [Display omitted] • Exploring the effects of different amides on the diffusion of amine monomers. • Longer chain DMPr contributes to the formation of multilayered nanovoid structures. • Correlating amine monomer diffusion rate with PA layer evolution. • TFC a-o -DMPr shows water permeability of 2.26 LMH/bar and NaCl rejection of 98.38 %. [ABSTRACT FROM AUTHOR]

Embedding nanomaterials in thin film composite membranes to overcome the dynamic balance between salt rejection and permeability has become a research hotspot. Apparently, the filling positions of nanomaterials in membranes have a significant influence on membrane properties. In this work, GO@CS core-shell nanomaterials was firstly successfully synthesized, with good hydrophilicity and fast water transmission channels. Then the influences of addition amounts and loading positions of GO@CS on membrane performance were explored. Results demonstrated that embedding GO@CS with 0.01 wt% in the polyamide layer could give full play to the advantages of core-shell nanomaterials and improve the water flux and salt rejection (water flux increased by 115%, salt rejection increased to 99.10%), as well as the performance stability. Compared with TFN membrane with GO@CS embedded between the polyamide layer and supporting layer, the TFN membrane with GO@CS embedded in the polyamide layer could make full use of advantages provided by GO@CS that fast water transmission channels and the interlayer spacing assisting in salt rejection. This work provided guidances for the effect of nanomaterials with hierarchical pores embedding position on membrane performance. Image 1 • GO@CS core-shell nanomaterials were synthesized. • TFN membranes with different loading positions of GO@CS were prepared. • TFN-M membranes showed higher water flux and NaCl rejection. [ABSTRACT FROM AUTHOR]

Thin film nanocomposite (TFN) organic solvent nanofiltration (OSN) membrane with improved separation performance was fabricated via interfacial polymerization reaction between amine-functionalized graphene quantum dots (af-GQDs) doped aqueous monomer solution of m -phenylenediamine (MPD) and n -hexane solution containing trimesoyl chloride (TMC) monomer. We emphasize the employment of extra-low content for both af-GQDs and MPD, so that we could maximize the function of these nanomaterials and eliminate their aggregation at the same time. The af-GQDs nanomaterials could regulate the interfacial polymerization process and could be strongly anchored in the polyamide film via covalent bonding, hence could prevent their loss while providing more channels for faster solvent penetration. As a result, the optimized OSN membrane, TFN-50, shows a super-smooth surface, with a surface roughness as low as 4.3 ± 0.2 nm, and excellent pure solvent permeances which reach 135.8, 112.7, and 69.8 L m−2 h−1 MPa−1 for methanol, DMF and ethanol, respectively, as well as a very high Rhodamine B (RDB, 479 Da) rejection of up to 99.2%, and an ethanol permeance of 61.4 L m−2 h−1 MPa−1. Furthermore, the TFN-50 OSN membrane still shows excellent filtration performance after being submerged in DMF for 336 h or continuous crossflow filtration with Rose bengal (RB, 1017 Da)/DMF solution for 136 h, demonstrating its excellent solvent resistance. [Display omitted] • TFN OSN membrane incorporated with af-GQDs nanomaterials is prepared via interfacial polymerization method. • Ultra-low content for af-GQDs and MPD is used in the aqueous phase during the interfacial polymerization process. • Af-GQDs effectively manipulate the interfacial polymerization process and help to form a selectivity layer with ultra-smooth surface. • Higher solvent permeance and excellent dye rejection performance are achieved with the aid of af-GQDs. • The af-GQDs doped OSN membrane has excellent durability performance in harsh strong polar solvents. [ABSTRACT FROM AUTHOR]

Solvent resistant nanofiltration (SRNF) membranes are highly demanded in processing organic solutions especially those contain large molecules with molecular weight between 200 to 2000 Da, yet they have some drawbacks such as relatively poor solvent resistance and low solvent permeance. The current work presented an innovative class of amino-functionalized graphene quantum dots (aGQDs) embedded thin film nanocomposites (TFN) for SRNF membranes which were prepared via interfacial polymerization (IP) and subsequent steps (chemical imidization, crosslinking, and solvent activation). The prepared membranes enabled covalent interactions not only between the IP skin layer and the substrate, but also between the IP layer and the embedded aGQDs. The ethanol permeance and surface porosity increased by 44% and 69%, respectively, with the embedment of aGQDs under the optimal conditions, while the Rhodamine B (RDB, 479 Da) rejection maintained essentially stable above 99%. Furthermore, our novel membranes exhibited excellent long-term stability, with a rejection of over 99% for Rose Bengal (RB, 1017 Da) during the continuous filtration of 100 mg L−1 RB/ N , N -dimethyl formamide (DMF) solution at room temperature for more than 768 h. They also exhibited good organic solvent resistance and high-temperature tolerance in both DMF and NMP solvents, with a RDB rejection of over 99% and an ethanol permeance of about 38 L m−2 h−1 MPa−1 after being immersed in DMF at 80 oC for 248 h, and a RDB rejection of over 99% and an ethanol permeance of about 41 L m−2 h−1 MPa−1 after being immersed in NMP at 80 oC for 232 h. The results demonstrated that the aGQDs-embedded TFN OSN membrane has vast potential in SRNF applications. Image 1 • (PI-aGQDs/PI) XA membrane was prepared via IP, imidization, crosslinking, activation. • The (PI-aGQDs/PI) XA SRNF membrane owns a wholly covalent bonding chemical structure. • aGQDs improve greatly the surface morphology and performance of the SRNF membrane. • The SRNF membranes kept >99% RB rejection in filtration of DMF at 25 oC for 30 days. • The SRNF membranes kept good solvent resistance in DMF and NMP at 80 oC for 10 days. [ABSTRACT FROM AUTHOR]