Advancing water treatment sustainability: Investigating electrified Ti3C2Tx composite membranes for minimizing microplastic fouling.

The overuse of plastics has led to a large influx of microplastics (MPs) in water bodies and water/wastewater treatment plants. Coupled with the ongoing water crisis, this poses a threat to freshwater availability as MPs disrupt the operation of these plants. MPs cause severe fouling of low-pressure membrane technologies such as ultrafiltration (UF) due to the strong adhesion between MPs and the membrane surface. An electrified membrane-based technology is suggested as an alternative MP fouling mitigation strategy. In this study, composite membranes of sulfonated polyethersulfone (SPES)/MXene (Ti3C2Tx) were fabricated and evaluated as a promising candidate for mitigating fouling of MPs. The described SPES/Ti3C2Tx composite membrane was designed to improve important physiochemical properties such as conductivity without affecting water flux. The membranes were tested under different electrical potentials to find an optimal strategy to reduce MP fouling. The performance tests showed that the flux increased from 42 L m-2. h-1 at 0 V to 49 L m-2. h-1 at 2 V due to electrostatic repulsion when 5 wt% Ti3C2Tx was used as a result of the applied electric potential. In addition, it was shown that intermittent applied voltage using "30 min ON: 60 min OFF" mode resulted in more stable water flux due to in-situ coagulant formation and cleaning. This study illustrates the potential of MXene-based membranes for mitigating MP fouling and paves the way for future research on membrane materials that can enhance system performance.

Surveillance, distribution, and treatment methods of antimicrobial resistance in water: A review.

The World Health Organization (WHO) recognizes antimicrobial resistance (AMR) as a serious threat to human health. Scientists warn that the world is approaching a post-antibiotic era, in which antibiotics will be ineffective, and AMR infections may become a leading cause of death worldwide. Wastewater treatment plants (WWTPs) have been identified as hotspots for the spread and reproduction of AMR. This review focuses on the fate of AMR in WWTPs and advanced water treatment processes, highlighting their removal efficiencies and limitations. Additionally, methods for monitoring AMR in WWTPs and aquatic environments are discussed. Monitoring of AMR in wastewater is crucial for tracking its presence and spread to the environment. Advanced AMR treatment processes such as membrane bioreactors (MBRs), vermifiltration (VF), advanced oxidation processes (AOPs), and membrane filtration processes (MFPs) are discussed and compared.

Cross-linked laminar graphene oxide membranes for wastewater treatment and desalination: A review.

Two-dimensional (2D) lamellar graphene oxide (GO) membranes are emerging as attractive materials for molecular separation in water treatment because of their single atomic thickness, excellent hydrophilicity, large specific surface areas, and controllable properties. To yet, commercialization of GO laminar membranes has been hindered by their propensity to swell in hydrated conditions. Thus, chemical crosslinking of GO sheets with the polymer matrix is used to improve GO membrane hydration stability. This review focuses on pertinent themes such as how chemical crosslinking improves the hydration stability, separation performance, and antifouling properties of GO membranes.

Enhanced water flux and bacterial resistance in cellulose acetate membranes with quaternary ammoniumpropylated polysilsesquioxane.

An enhanced water flux and anti-fouling nanocomposite ultrafiltration membrane based on quaternary ammoniumpropylated polysilsesquioxane (QAPS)/cellulose acetate (QAPS@CA) was fabricated by in situ sol-gel processing via phase inversion followed by quaternization with methyl iodide (CH3I). Membrane characterizations were performed based on the contact angle, FTIR, SEM, and TGA properties. Membrane separation performance was assessed in terms of pure water flux, rejection, and fouling resistance. The 7%QAPS@CA nanocomposite membrane showed an increased wettability (46.6° water contact angle), water uptake (113%) and a high pure water permeability of ∼370 L m-2 h-1 bar-1. Furthermore, the 7%QAPS@CA nanocomposite membrane exhibited excellent bactericidal properties (∼97.5% growth inhibition) against Escherichia coli (E. coli) compared to the bare CA membrane (0% growth inhibition). The 7%QAPS@CA nanocomposite membrane can be recommended for water treatment and biomedical applications.

Chitosan/Lignosulfonate Nanospheres as "Green" Biocide for Controlling the Microbiologically Influenced Corrosion of Carbon Steel.

In this work, uniform cross-linked chitosan/lignosulfonate (CS/LS) nanospheres with an average diameter of 150-200 nm have been successfully used as a novel, environmentally friendly biocide for the inhibition of mixed sulfate-reducing bacteria (SRB) culture, thereby controlling microbiologically influenced corrosion (MIC) on carbon steel. It was found that 500 µg·mL-1 of the CS/LS nanospheres can be used efficiently for the inhibition of SRB-induced corrosion up to a maximum of 85% indicated by a two fold increase of charge transfer resistance (Rct) on the carbon steel coupons. The hydrophilic surface of CS/LS can readily bind to the negatively charged bacterial surfaces and thereby leads to the inactivation or damage of bacterial cells. In addition, the film formation ability of chitosan on the coupon surface may have formed a protective layer to prevent the biofilm formation by hindering the initial bacterial attachment, thus leading to the reduction of corrosion.

Large interlayer spacing Nb4C3T x (MXene) promotes the ultrasensitive electrochemical detection of Pb2+ on glassy carbon electrodes.

A Nb4C3T x (MXene)-modified glassy carbon electrode was used for the electrochemical detection of Pb2+ ions in aqueous media. The sensing platform was evaluated by anodic stripping analysis after optimizing the influencing factors such as pH, deposition potential, and time. The large interlayer spacing, high c lattice parameter and higher conductivity of Nb4C3T x compared to other MXenes enhance the electrochemical detection of Pb2+. The developed sensor can reach a detection limit of 12 nM at a potential ∼-0.6 V. Additionally, the developed sensor showed promising selectivity in the presence of Cu2+ and Cd2+, and stability for at least 5 cycles of continuous measurements with good repeatability. This work demonstrates the potential applications of Nb4C3T x towards the development of effective electrochemical sensors.

Graphene oxide based nanohybrid proton exchange membranes for fuel cell applications: An overview.

In the context of many applications, such as polymer composites, energy-related materials, sensors, 'paper'-like materials, field-effect transistors (FET), and biomedical applications, chemically modified graphene was broadly studied during the last decade, due to its excellent electrical, mechanical, and thermal properties. The presence of reactive oxygen functional groups in the grapheme oxide (GO) responsible for chemical functionalization makes it a good candidate for diversified applications. The main objectives for developing a GO based nanohybrid proton exchange membrane (PEM) include: improved self-humidification (water retention ability), reduced fuel crossover (electro-osmotic drag), improved stabilities (mechanical, thermal, and chemical), enhanced proton conductivity, and processability for the preparation of membrane-electrode assembly. Research carried on this topic may be divided into protocols for covalent grafting of functional groups on GO matrix, preparation of free-standing PEM or choice of suitable polymer matrix, covalent or hydrogen bonding between GO and polymer matrix etc. Herein, we present a brief literature survey on GO based nano-hybrid PEM for fuel cell applications. Different protocols were adopted to produce functionalized GO based materials and prepare their free-standing film or disperse these materials in various polymer matrices with suitable interactions. This review article critically discussed the suitability of these PEMs for fuel cell applications in terms of the dependency of the intrinsic properties of nanohybrid PEMs. Potential applications of these nanohybrid PEMs, and current challenges are also provided along with future guidelines for developing GO based nanohybrid PEMs as promising materials for fuel cell applications.

2-Acrylamido-2-methyl-1-propanesulfonic Acid Grafted Poly(vinylidene fluoride-co-hexafluoropropylene)-Based Acid-/Oxidative-Resistant Cation Exchange for Membrane Electrolysis.

For developing acid-/oxidative-resistant aliphatic-polymer-based cation-exchange membrane (CEM), macromolecular modification of poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-co-HFP) was carried out by controlled chemical grafting of 2-acrylamido-2-methyl-1-propanesulfonic acid (AMPS). To introduce the unsaturation suitable for chemical grafting, dehydrofluorination of commercially available PVDF-co-HFP was achieved under alkaline medium. Sulfonated copolymer (SCP) was prepared by the free radical copolymerization of dehydofluorinated PVDF-co-HFP (DHPVDF-co-HFP) and AMPS in the presence of free radical initiator. Prepared SCP-based CEMs were analyzed for their morphological characteristics, ion-exchange capacity (IEC), water uptake, conductivity, and stabilities (mechanical, chemical, and thermal) in comparison with state-of-art Nafion117 membrane. High bound water content avoids the membrane dehydration, and most optimal (SCP-1.33) membrane exhibited about ∼2.5-fold high bound water content in comparison with that of Nafion117 membrane. Bunsen reaction of iodine-sulfur (I-S) was successfully performed by direct-contact-mode membrane electrolysis in a two-compartment electrolytic cell using different SCP membranes. High current efficiency (83-99%) confirmed absence of any side reaction and 328.05 kJ mol-H2(-1) energy was required for to produce 1 mol of H2 by electrolytic cell with SCP-1.33 membrane. In spite of low conductivity for reported SCP membrane in comparison with that of Nafion117 membrane, SCP-1.33 membrane was assessed as suitable candidate for electrolysis because of its low-cost nature and excellent stabilities in highly acidic environment may be due to partial fluorinated segments in the membrane structure.

Sulfonated polyimide/acid-functionalized graphene oxide composite polymer electrolyte membranes with improved proton conductivity and water-retention properties.

Sulfonated polyimide (SPI)/sulfonated propylsilane graphene oxide (SPSGO) was assessed to be a promising candidate for polymer electrolyte membranes (PEMs). Incorporation of multifunctionalized (-SO3H and -COOH) SPSGO in SPI matrix improved proton conductivity and thermal, mechanical, and chemical stabilities along with bound water content responsible for slow dehydration of the membrane matrix. The reported SPSGO/SPI composite PEM was designed to promote internal self-humidification, responsible for water-retention properties, and to promote proton conduction, due to the presence of different acidic functional groups. Strong hydrogen bonding between multifunctional groups thus led to the presence of interconnected hydrophobic graphene sheets and organic polymer chains, which provides hydrophobic-hydrophilic phase separation and suitable architecture of proton-conducting channels. In single-cell direct methanol fuel cell tests, SPI/SPSGO-8 exhibited 75.06 mW·cm(-2) maximum power density (in comparison with commercial Nafion 117 membrane, 62.40 mW·cm(-2)) under 2 M methanol fuel at 70 °C.

Synthesis and bioefficacy evaluation of new 3-substituted-3,4-dihydro-1,3-benzoxazines.

A new series of 1, 3-Benzoxazines were synthesized, characterized ((1)H NMR and (13)C NMR) and evaluated for their pesticidal activity. Six new 3-alkyl-3, 4-dihydro-4-methyl-2H-1, 3-benzoxazines (1-6) were prepared by hydroxymethylation of secondary amines with formaldehyde in 65-68% yields. These compounds were screened for there IGR activity against Spodoptera litura and for antifungal fungal activity in vitro against Sclerotium rolfsii ITCC 6181 by poisoned food technique. Insect Growth Regulatory (IGR) activity against Spodoptera litura showed that compound 3-Nonyl-3,4-dihydro-4-methyl-2H-1,3-benzoxazines was most effective as IGR with larval GI(50) of 1.863 mu g/Insect. Compounds 3-Octyl-3,4-dihydro-4-methyl-2H-1,3-benzoxazines and 3-Decyl-3,4-dihydro-4-methyl-2H-1,3-benzoxazines were effective IGRs. Antifungal screening revealed that compound 3-Dodecyl-3, 4-dihydro-4-methyl-2H-1,3-benzoxazines, was highly effective against Sclerotium rolfsii with LC(50) value 31.7 mg L(-1) comparable with commercial fungicide Hexaconazole (LC(50) 1.27 mg L(-1)). Also compounds 3-Nonyl-3, 4-dihydro-4-methyl-2H-1,3-benzoxazines and 3-Decyl-3,4-dihydro-4-methyl-2H-1,3-benzoxazines displayed promising fungitoxicity. The results described in this paper are promising and provides new array of synthetic chemicals to be utilized as pesticides.

Development of controlled release formulations of azadirachtin-A employing poly(ethylene glycol) based amphiphilic copolymers.

Controlled release (CR) formulations of azadirachtin-A, a bioactive constituent derived from the seed of Azadirachta indica A. Juss (Meliaceae), have been prepared using commercially available polyvinyl chloride, polyethylene glycol (PEG) and laboratory synthesized poly ethylene glycol-based amphiphilic copolymers. Copolymers of polyethylene glycol and various dimethyl esters, which self assemble into nano micellar aggregates in aqueous media, have been synthesized. The kinetics of azadirachtin-A, release in water from the different formulations was studied. Release from the commercial polyethylene glycol (PEG) formulation was faster than the other CR formulations. The rate of release of encapsulated azadirachtin-A from nano micellar aggregates is reduced by increasing the molecular weight of PEG. The diffusion exponent (n value) of azadirachtin-A, in water ranged from 0.47 to 1.18 in the tested formulations. The release was diffusion controlled with a half release time (t(1/2)) of 3.05 to 42.80 days in water from different matrices. The results suggest that depending upon the polymer matrix used, the application rate of azadirachtin-A can be optimized to achieve insect control at the desired level and period.