Given the huge potential of thin film composite (TFC) nanofiltration (NF) membranes for desalination and micro-pollutant removal, two different sets of six NF membranes were synthesized. The molecular structure of the polyamide active layer was tuned by using two different cross-linkers, terephthaloyl chloride (TPC) and trimesoyl chloride (TMC), reacted with tetra-amine solution containing β-Cyclodextrin (BCD). To further tune the structure of the active layers, the time duration of interfacial polymerization (IP) was varied from 1 to 3 min. The membranes were characterized by scanning electron microscopy (SEM), atomic force microscopy (AFM), water contact angle (WCA), attenuated total reflectance Fourier transform infra-red (ATR-FTIR) spectroscopy, elemental mapping and energy dispersive (EDX) analysis. The six fabricated membranes were tested for their ability to reject divalent and monovalent ions followed by rejection of micro-pollutants (pharmaceuticals). Consequently, terephthaloyl chloride turned out to be the most effective crosslinker for the fabrication of membrane active layer with tetra-amine in the presence of β-Cyclodextrin using interfacial polymerization reaction for 1 min. The membrane fabricated using TPC crosslinker (BCD-TA-TPC@PSf) showed higher % rejection for divalent ions (NaSO = 93%; MgSO = 92%; MgCl = 91%; CaCl = 84%) and micro-pollutants (Caffeine = 88%; Sulfamethoxazole = 90%; Amitriptyline HCl = 92%; Loperamide HCl = 94%) compared to the membrane fabricated using TMC crosslinker (BCD-TA-TMC@PSf). For the BCD-TA-TPC@PSf membrane, the flux was increased from 8 LMH (L/m.h) to 36 LMH as the transmembrane pressure was increased from 5 bar to 25 bar.
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http://dx.doi.org/10.3390/membranes13050528 | DOI Listing |
Sci Rep
December 2024
Department of Mechanical Engineering, Carnegie Mellon University, Pittsburgh, PA, USA.
Polymer electrolyte membrane water electrolyzers (PEMWEs) are a critical technology for efficient hydrogen production to decarbonize fuels and industrial feedstocks. To make hydrogen cost-effective, the overpotentials across the cell need to be decreased and platinum-group metal loading reduced. One overpotential that needs to be better understood is due to mass transport limitations from bubble formation within the porous transport layer (PTL) and anode catalyst layer (ACL), which can lead to a reduction in performance at typical operating current densities.
View Article and Find Full Text PDFNat Commun
December 2024
Imperial College Parturition Research Group, Institute of Reproductive and Developmental Biology, Department of Metabolism Digestion and Reproduction, Imperial College London, London, UK.
Lactobacillus species dominance of the vaginal microbiome is a hallmark of vaginal health. Pathogen displacement of vaginal lactobacilli drives innate immune activation and mucosal barrier disruption, increasing the risks of STI acquisition and, in pregnancy, of preterm birth. We describe differential TLR mediated activation of the proinflammatory transcription factor NF-κB by vaginal pathogens and commensals.
View Article and Find Full Text PDFNat Commun
December 2024
Jiangsu Co-Innovation Center of Efficient Processing and Utilization of Forest Resources, Nanjing Forestry University, Nanjing, 210037, China.
Carbon nanomaterials show outstanding promise as electrocatalysts for hydrogen peroxide (HO) synthesis via the two-electron oxygen reduction reaction. However, carbon-based electrocatalysts that are capable of generating HO at industrial-level current densities (>300 mA cm) with high selectivity and long-term stability remain to be discovered. Herein, few-layer boron nanosheets are in-situ introduced into a porous carbon matrix, creating a metal-free electrocatalyst (B-C) with HO production rates of industrial relevance in neutral or alkaline media.
View Article and Find Full Text PDFAdv Mater
December 2024
State Key Lab of High Performance Ceramics and Superfine Microstructure, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai, 200050, P. R. China.
Nickel-iron layered double hydroxides (NiFe LDHs) are considered as promising substitutes for precious metals in oxygen evolution reaction (OER). However, most of the reported NiFe LDHs suffer from poor long-term stability because of the Fe loss during OER resulting in severe inactivation. Herein, a dynamically stable chelating interface through in situ transformation of asymmetric aldehyde-ligand (THB, 1,3,5-Tris(3'-hydroxy-4'-formylphenyl)-benzene) modified NiFe LDHs to anchor Fe and significantly enhance the OER stability is reported.
View Article and Find Full Text PDFSmall Methods
December 2024
Institute of Advanced Synthesis (IAS) and School of Chemistry and Molecular Engineering, Jiangsu National Synergetic Innovation Centre for Advanced Materials, Nanjing Tech University, Nanjing, 211816, China.
The selective Au deposition at the Au-substrate interface is known to give ultrathin Au nanowires and the synthesis usually employs strong thiol-based ligands. It is shown that, by increasing the rate of Au deposition, weak cetyltrimethylammonium bromide (CTAB) can be made to behave like a strong ligand, so that it induces Active Surface Growth and gives Au nanowires. The ligand strength also depends on the packing interactions in the ligand layer, in the order of CTAB, CTAB, and CTAB.
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