Antifouling polymeric nanocomposite membrane based on interfacial polymerization of polyamide enhanced with green TiO2 nanoparticles for water desalination

In the present investigation, the preparation and characterization of polyamide/TiO2 as thin film nanocomposites (TFN) for brackish water desalination was investigated. TiO2 nanoparticles (NPs) were synthesized by a green method using thyme plant extract as a reducing and capping agent. The TiO2 NPs was successfully prepared in pure crystalline anatase phase with 15 nm size, and −33.1 mV zeta potential. The antimicrobial tests confirmed the antimicrobial activity of TiO2 against gram-positive and gram-negative bacteria. In addition, TiO2 NPs showed a good photocatalytic activity in degradation of methylene blue dye. TFN based on interfacial polymerization was enhanced by embedding 5% of the greenly synthesized TiO2 NPs within the polyamide thin film active layer. The incorporation of TiO2 NPs was confirmed by SEM, atomic force microscope (AFM), surface wettability, and FTIR. Membranes performance was investigated based on flux, salt rejection and fouling resistance. The antifouling was examined using bovine serum albumin (BSA) as protein fouling by dead-end cell filtration system at 2 bar. The results showed the TFN increased in water flux by 40.9% and a slight decrease in NaCl rejection (6.3%) was observed, with enhancement in antifouling properties. The flux recovery rate of the modified TFN membranes after fouling with BSA solution was enhanced by 21.5% (from 61.7% for TFC to 83.2% for TFN). Also, they demonstrated remarkable anti-biofouling behavior against both bacterial strains

E/Z reversible photoisomerization of methyl orange doped polyacrylic acid-based polyelectrolyte brush films

The photoswitching behavior of the polyacrylic acid (PAA) doped by methyl orange (MO) brush film was investigated using spectral analysis of UV-Vis absorbance, Fourier Transformation Infrared spectroscopy, 2D electrical conductivity mapping and Atomic Force Microscopy. The kinetics and time evolution of the photoisomerization of the PAA-MO PEBs film from E-state to Z-state by UV-light irradiation, and reverse thermal relaxation to E-state was explored. The results confirm that the photoisomerization kinetics of the overall peak is the superposition of the photoisomerization kinetics of (Formula presented.) transition, low- and high-frequency of the (Formula presented.) transition bands. The E–Z transformation led to transforming the azobenzene from flat with no dipole moment to 3.0 D dipole moment. Hence, the electrical conductivity escalated accordingly. The transformation of E-state to Z-state led to the collapse of the formed brushes because of the angular rotational momentum consequent to E–Z isomerization

Biosynthesis and Characterization of Zinc Oxide Nanoparticles (ZnO-NPs) Utilizing Banana Peel Extract

In recent years, there has been a significant focus on the green synthetization of metal oxide nanoparticles due to their environmentally friendly features and cost-effectiveness. The aim of this study is to biosynthesize zinc oxide nanoparticles (ZnO NPs) through a green method, utilizing crude banana peel extract as reducing and capping agents, to characterize the synthesized ZnO NPs and test their antibacterial activity. ZnO NPs were biosynthesized using the peel extract of banana with various concentrations of zinc acetate dihydrate salt, followed by annealing at 400 °C for 2 h. The synthesized ZnO NPs were characterized using UV–visible spectroscopy (UV-Vis), scanning electron microscopy (SEM), dynamic light scattering (DLS), attenuated total reflectance–Fourier-transform infrared (ATR-FTIR), and X-ray diffraction (XRD). Also, its antibacterial efficiency against different bacterial strains was tested. ZnO NPs were biosynthesized successfully using the extract of Musa Acumniata (cavendish) fruit peel with a UV-Vis wavelength range of 344 to 369 nm and an electrical band gap ranging from 3.36 to 3.61 eV. The size varied from 27 ± 4 nm to 89 ± 22, and the negative zeta potential (ζ) ranged from −14.72 ± 0.77 to −7.43 ± 0.35 mV. ATR-FTIR analysis showed that the extract phytochemical functional groups were present on ZnO NPs. XRD results confirm the formation of a highly pure wurtzite hexagonal structure of ZnO NPs. Moreover, the best obtained size of ZnO NPs was selected for the antibacterial tests, giving the highest inhibition growth rate against Staphylococcus epidermidis (98.6 ± 0.9%), while the lowest rate was against Pseudomonas aeruginosa (88.4 ± 4.4%). The minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) were reported and compared to previous studies. The unique properties of greenly synthesized ZnO NPs and their antibacterial activity have potential for reducing environmental pollution and the use of antibiotics, which may contribute to solving the problem of bacterial resistance. Therefore, studies that aim to design an applicable dosage form loaded with biosynthesized ZnO NPs might be conducted in the future

Photodegradation of Carbol Fuchsin Dye Using an Fe2−xCuxZr2−xWxO7 Photocatalyst under Visible-Light Irradiation

Fe2−xCuxZr2−xWxO7 (x: 0, 0.05, 0.015) nanoparticles were synthesized following the Pechini method and characterized via X-ray diffraction (XRD), transmission electron microscopy (TEM), and diffuse reflectance spectroscopy (DRS) measurements to be used as photocatalysts in colored water remediation. All of the prepared materials were crystallized in a cubic fluorite phase as the major phase. The band gap was reduced upon doping with W6+ and Cu2+ from 1.96 eV to 1.47 eV for Fe1.85Cu0.15Zr1.85W0.15O7. Carbol fuchsin (CF) dye was used to determine the photocatalytic degradation efficiency of the prepared catalysts. Degradation efficiency was directly proportional to the dopant’s concentration. Complete removal of 20 mg/L CF was achieved under optimal conditions (pH 9, and catalyst loading of 1.5 g/L) using Fe1.85Cu0.15Zr1.85W0.15O7. The degradation rate followed pseudo-first-order kinetics. The reusability for photocatalysts was tested five times, decreasing its efficiency by 4% after the fifth cycle, which indicates that the prepared Fe1.85Cu0.15Zr1.85W0.15O7 photocatalyst is a promising novel photocatalyst due to its superior efficiency in dye photodegradation

A study on removal characteristics of <i>o</i>-, <i>m</i>-, and <i>p</i>-nitrophenol from aqueous solutions by organically modified diatomaceous earth

<div><p></p><p>The natural diatomaceous earth (DAT) was modified with surfactant of hexadecyltrimethylammonium bromide (HDTMABr) to form organic-modified diatomaceous earth (DAT-HDTMABr). The DAT and DAT-HDTMABr were characterized by X-ray fluorescence, X-ray diffraction, FT-IR and DTA-TG. The surface area was determined using Brunauer, Emmett, and Teller adsorption method. Cation exchange capacity was estimated using an ethylenediamine complex of copper method, and the modifier loading was calculated from the total carbon analysis. The ability of raw and organomodified diatomaceous earth to remove <i>o</i>-nitrophenol (ONP), <i>m</i>-nitrophenol (MNP), and <i>p</i>-nitrophenol (PNP) from aqueous solutions has been carried out at predetermined equilibration time, adsorbent amount, pH, and temperatures using a batch technique. The removal of ONP, MNP, and PNP from aqueous solutions by modified clay seems to be more effective than unmodified sample. The experimental equilibrium adsorption data were analyzed by four widely used two parameters, Langmuir, Freundlich, Temkin, and Dubinin–Radushkevich (D–R) isotherm equations. Kinetic studies showed that pseudo-second-order described the adsorption experimental data better than the pseudo-first-order kinetic model. Based on the calculated thermodynamic parameters, such as enthalpy (Δ<i>H</i>), entropy (Δ<i>S</i>), and Gibb’s free energy changes (Δ<i>G</i>), it is noticeable that the adsorption of ONP, MNP, and PNP by DAT and DAT-HDTMABr adsorbents was carried out spontaneously, and the process was exothermic in nature.</p></div