Search

This study synthesized three MoS₂ morphologies—nanospheres, nanoplatelets, and nanosheets—under varied conditions and incorporated them into chitosan membranes. TEM confirmed unique morphologies and crystallinity. Clean water flux showed that the nanoplatelet (P-CM) membrane had the highest flux due to higher porosity. The P-CM membrane excelled in removing Mn²⁺ and Zn²⁺ ions, achieving 93.0 ± 0.5% and 90.4 ± 1.5% removal, outperforming membranes with nanospheres (S-CM) and nanosheets (T-CM). Its superior performance is attributed to thicker nanoplatelets forming more water channels. The MoS₂'s tri-layered structure generated reactive oxygen species (ROS) via H₂O₂ catalysis, contributing to enhanced heavy metal removal. These adsorptive-catalytic membranes combine adsorption with catalytic decomposition of heavy metals, highlighting the work's novelty and superior performance. The membranes demonstrated excellent flux recovery and reusability (96.0 ± 0.5% for P-CM) after chemical cleaning. The findings emphasize the impact of nanomaterial morphologies on membrane performance in water treatment and environmental remediation. [ABSTRACT FROM AUTHOR]

In this work, the fouling resistance of TFC (thin film composite) nanofiltration membranes have been enhanced using an electrostatically coupled SiO2 (silica dioxide) nanoparticles/poly(L-DOPA) (3-(3,4-dihydroxyphenyl)-l-alanine) antifouling coating. SiO2 nanoparticles were synthesized in different size ranges and combined with L-DOPA; and then coated as an anti-fouling layer on the membrane surface by recirculated deposition. Membranes were coated with S-NP (silica nanoparticles) in small (19.8 nm), medium (31.6 nm) and large (110.1 nm) sizes. The zwitterionic compound L-DOPA in the form of self-polymerized poly(L-DOPA) (PDOPA) helped with the attachment of the S-NP to the membrane surface. It was confirmed by AFM (atomic force microscopy) measurement that coating of membranes led to an increase in hydrophilicity and reduction in surface roughness, which in turn led to a 60% reduction in the adhesion force of the foulant on the membrane as compared to the neat membrane. The modified membranes experienced almost no flux decline during the filtration experimental period, whereas the unmodified membrane showed a sharp flux decline. The best coating conditions of silica nanoparticles resulting in enhanced anti-fouling properties were identified. The biofouling film formation on the membranes was evaluated quantitatively using the flow cytometry method. The results indicated that the modified membranes had 50% lower microbial population growth in terms of total event count compared to the neat membrane. Overall, the experimental results have confirmed that the coating of electrostatically coupled SiO2 nanoparticles and PDOPA (S-NP/PDOPA) on TFC-NF (nanofiltration) membrane surfaces is effective in improving the fouling resistance of the membranes. This result has positive implications for reducing membrane fouling in desalination and industrial wastewater treatment applications. [ABSTRACT FROM AUTHOR]

MoS 2 nanosheets were synthesized by a bottom-up green chemical process where l-cysteine was used as a sulfur precursor. With specific concentrations, molar ratio of reactants, and pre-mixing conditions, MoS 2 nanosheets of 200-300 nm in size and 4.2 nm in average thickness were successfully obtained. Porous membranes were then prepared by depositing the MoS 2 nanosheet suspension on a 0.1 μm pore size poly(vinylidene difluoride) membrane filter in a multiple batch procedure. The membrane deposited with 12 batches of MoS 2 nanosheets achieved 93.78% removal of bovine serum albumin. Acid red removal of 95.65% was also achieved after the second filtration pass. The porous MoS 2 nanosheet membrane also demonstrated a high water flux of 182 ± 2.0 L/(m 2 h). This result overcame the trade-off between selectivity and permeability faced by polymeric ultrafiltration membranes. The MoS 2 nanosheets as building blocks formed not only intersheet slit pores with a narrow half-width to restrict the passage of organic molecules but also macro-channels allowing easy passage of water. The assembled MoS 2 nanosheet membrane delivered promising separation of protein molecules and a high flux, attributing to its porous nanostructure, and could be a potential membrane for various water applications., Competing Interests: The authors declare no competing financial interest., (© 2022 The Authors. Published by American Chemical Society.)

2D Molybdenum disulfide (MoS 2 ) nanoplatelets were synthesized via a green bottom-up strategy using non-toxic l-Cysteine as sulfur source. Thehydrophobic MoS 2 nanoplatelets assisted by hydrophilic 3-(3, 4-dihydroxyphenyl)-l-alanine (l-DOPA) were coated on a thin film composite nanofiltration (TFC-NFG) membrane. The accelerated fouling experiments were conducted by usingbovine serum albumin (BSA) asmodel organic foulant,and MoS 2 coated membrane demonstrated excellent resistance with almost no flux decline within first hour of filtration, whereas the uncoated membrane showed flux decline immediately from the beginning of the experiment. After 5-hour filtration, the flux reduced by only 26% for MoS 2 coated membrane with a higher flux recovery rate of 85.4% after washing by de-ionized (DI) water, whereas 45% flux decline was observed for uncoated membrane with lower flux recovery of 68%.These antifouling effects attributed by MoS 2 coated membrane were underpinned by combined unique interfacial properties offered by 2D tri-atomic layered MoS 2 morphology including dispersive surface tension, reduced surface roughness, weaker MoS 2 -foulant interactive forces, and negatively charged surface. This research positively confirms the role of 2D MoS 2 nanoplatelets as an anti-fouling coating on membranes and brings up more possibility for applying other nanomaterials in 2D family in water applications such as desalination and water treatment., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2021 Elsevier Inc. All rights reserved.)

In this work, the fouling resistance of TFC (thin film composite) nanofiltration membranes have been enhanced using an electrostatically coupled SiO 2 (silica dioxide) nanoparticles/poly(L-DOPA) (3-(3,4-dihydroxyphenyl)-l-alanine) antifouling coating. SiO 2 nanoparticles were synthesized in different size ranges and combined with L-DOPA; and then coated as an anti-fouling layer on the membrane surface by recirculated deposition. Membranes were coated with S-NP (silica nanoparticles) in small (19.8 nm), medium (31.6 nm) and large (110.1 nm) sizes. The zwitterionic compound L-DOPA in the form of self-polymerized poly(L-DOPA) (PDOPA) helped with the attachment of the S-NP to the membrane surface. It was confirmed by AFM (atomic force microscopy) measurement that coating of membranes led to an increase in hydrophilicity and reduction in surface roughness, which in turn led to a 60% reduction in the adhesion force of the foulant on the membrane as compared to the neat membrane. The modified membranes experienced almost no flux decline during the filtration experimental period, whereas the unmodified membrane showed a sharp flux decline. The best coating conditions of silica nanoparticles resulting in enhanced anti-fouling properties were identified. The biofouling film formation on the membranes was evaluated quantitatively using the flow cytometry method. The results indicated that the modified membranes had 50% lower microbial population growth in terms of total event count compared to the neat membrane. Overall, the experimental results have confirmed that the coating of electrostatically coupled SiO 2 nanoparticles and PDOPA (S-NP/PDOPA) on TFC-NF (nanofiltration) membrane surfaces is effective in improving the fouling resistance of the membranes. This result has positive implications for reducing membrane fouling in desalination and industrial wastewater treatment applications.