Constructing Positively Charged Thin-Film Nanocomposite Nanofiltration Membranes with Enhanced Performance.
Using polyethylenimine (PEI) as the aqueous reactive monomers, a positively charged thin-film nanocomposite (TFN) nanofiltration (NF) membrane with enhanced performance was developed by successfully incorporating graphene oxide (GO) into the active layer. The effects of GO concentrations on the surface roughness, water contact angle, water flux, salt rejection, heavy metal removals, antifouling property, and chlorine resistance of the TFN membranes were evaluated in depth. The addition of 20 ppm GO facilitated the formation of thin, smooth, and hydrophilic nanocomposite active layers. Thus, the TFN-PEI-GO-20 membrane showed the optimal water flux of 70.3 L·m−2·h−1 without a loss of salt rejection, which was 36.8% higher than the thin-film composite (TFC) blank membrane. More importantly, owing to the positively charged surfaces, both the TFC-PEI-blank and TFN-PEI-GO membranes exhibited excellent rejections toward various heavy metal ions including Zn2+, Cd2+, Cu2+, Ni2+, and Pb2+. Additionally, compared with the negatively charged polypiperazine amide NF membrane, both the TFC-PEI-blank and TFN-PEI-GO-20 membranes demonstrated superior antifouling performance toward the cationic surfactants and basic protein due to their hydrophilic, smooth, and positively charged surface. Moreover, the TFN-PEI-GO membranes presented the improved chlorine resistances with the increasing GO concentration.
- # Thin-Film Nanocomposite Nanofiltration Membranes
- # Graphene Oxide Concentration
- # Graphene Oxide
- # Increasing Graphene Oxide Concentration
- # Thin-Film Nanocomposite Nanofiltration
- # Nanocomposite Nanofiltration Membrane
- # Thin-Film Nanocomposite Membranes
- # Nanocomposite Nanofiltration
- # Blank Membrane
- # Chlorine Resistance
- Research Article
28
- 10.3390/polym10111253
- Nov 12, 2018
- Polymers
In order to develop a high-performance thin-film nanocomposite (TFN) nanofiltration (NF) membrane, the functionalized graphene-based nanomaterial (GO-HBE-COOH) was synthesized by combining two-dimensional graphene oxide (GO) with a three-dimensional hyperbranched polymer, which was used as the novel nanofiller and successfully embedded into the polypiperazine-amide (PPA) active layers on polysulfone (PSU) substrates via interfacial polymerization (IP) process. The resultant NF membranes were characterized using ATR-FTIR, SEM, and AFM, while their performance was evaluated in terms of water flux, salt rejection, antifouling ability, and chlorine resistance. The influence of GO-HBE-COOH concentration on the morphologies, properties, and performance of TFN NF membranes was investigated. With the addition of 60 ppm GO-HBE-COOH, the TFN-GHC-60 NF membrane exhibited the optimal water flux without a sacrifice of the salt rejection. It was found that the introduction of GO-HBE-COOH nanosheets favored the formation of a thinner and smoother nanocomposite active layer with an enhanced hydrophilicity and negative charge. As a result, TFN NF membranes demonstrated a superior permeaselectivity, antifouling ability, and chlorine resistance over the conventional PPA thin-film composite (TFC) membranes.
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39
- 10.1039/c9ew00963a
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168
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Removal of pharmaceutically active compounds (PhACs) is of great importance in wastewater reclamation due to their potent negative impacts on human health. Typical polyamide nanofiltration (NF) membranes are negatively charged, which compromises their rejection rate of positively charged PhACs. Herein, we propose to rationally design a novel thin-film nanocomposite (TFN) NF membrane featuring a dually charged metal organic framework (MOF) to effectively remove both positively and negatively charged PhACs. Ethylenediamine (ED) was grafted to the coordinately unsaturated metal sites inside the MIL-101(Cr). The resulting ED-MIL-101(Cr) contained both strong positively charged amine groups inside its channels and negatively charged carboxyl groups at its surface. This dually charged nature of the MOF nanoparticles enabled the ED-MIL-101(Cr)-containing TFN membrane to achieve high rejection rates (mostly >90%) for both positively (terbutaline, atenolol, fluoxetine) and negatively charged PhACs (ketoprofen, diclofenac, bezafibrate). At the same time, the ED-MIL-101(Cr) TFN membrane had greatly improved water permeance (140% over the control membrane with MOF loading). Calculations based on density functional theory further confirmed the large energy barrier for the migration of both negatively and positively charged PhACs across the nanochannels of ED-MIL-101(Cr). This study highlights a promising potential of dually charged MOF-TFN membranes for efficient removal of trace organic contaminants in wastewater reclamation.
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99
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