Solution Blowing Spinning Technology towards Green Development of Urea Sensor Nanofibers Immobilized with Hydrazone Probe

Cellulose has been one of the most widespread materials due to its renewability, excellent mechanical properties, biodegradability, high absorption ability, biocompatibility and cheapness. Novel, simple and green colorimetric fibrous film sensor was developed by immobilization of urease enzyme (U) and tricyanofuran hydrazone (TCFH) molecular probe onto cellulose nanofibers (CNF). Cellulose acetate nanofibers (CANF) were firstly prepared from cellulose acetate using the simple, green and low cost solution blowing spinning technology. The produced CANF was exposed to deacetylation to introduce CNF, which was then treated with a mixture of TCFH and urease enzyme to introduce CNF-TCFH-U nanofibrous biosensor. CNF were reinforced with tricyanofuran hyrazone molecular probe and urease enzyme was encapsulated into calcium alginate biopolymer to establish a biocomposite film. This CNF-TCFH-U naked-eye sensor can be applied as a disposable urea detector. CNF demonstrated a large surface area and was utilized as a carrier for TCFH, which is the spectroscopic probe and urease is a catalyst. The biochromic CNF-TCFH-U nanofibrous biosensor responds to an aqueous medium of urea via a visible color signal changing from off-white to dark pink. The morphology of the generated CNF and CNF-TCFH-U nanofibrous films were characterized by different analytical tools, including energy-dispersive X-ray patterns (EDX), polarizing optical microscope (POM), Fourier-transform infrared spectroscopy (FT-IR) and scanning electron microscope (SEM). SEM images of CNF-TCFH-U nanofibers demonstrated diameters between 800 nm and 2.5 μm forming a nonwoven fabric with a homogeneous distribution of TCFH/urease-containing calcium alginate nanoparticles on the surface of CNF. The morphology of the cross-linked calcium alginate nanoparticles was also explored using transmission electron microscopy (TEM) to indicate an average diameter of 56–66 nm. The photophysical performance of the prepared CNF-TCFH-U was also studied by CIE Lab coloration parameters. The nanofibrous film biosensor displayed a relatively rapid response time (5–10 min) and a limit of detection as low as 200 ppm and as high as 1400 ppm. Tricyanofuran hydrazone is a pH-responsive disperse dye comprising a hydrazone detection group. Determination of urea occurs through a proton transfer from the hydrazone group to the generated ammonia from the reaction of urea with urease

Oxidation of Phenol by Hydrogen Peroxide Catalyzed by Metal-Containing Poly(amidoxime) Grafted Starch

Polyamidoxime chelating resin was obtained from polyacrylonitrile (PAN) grafted starch. The nitrile groups of the starch-grafted polyacrylonitrile (St-g-PAN) were converted into amidoximes by reaction with hydroxylamine under basic conditions. The synthesized graft copolymer and polyamidoxime were characterized by FTIR, TGA and elemental microanalysis. Metal chelation of the polyamidoxime resin with iron, copper and zinc has been studied. The produced metal-polyamidoxime polymer complexes were used as catalysts for the oxidation of phenol using H2O2 as oxidizing agent. The oxidation of phenol depends on the central metal ion present in the polyamidoxime complex. Reuse of M-polyamidoxime catalyst/H2O2 system showed a slight decrease in catalytic activities for all M-polyamidoxime catalysts

Preparation of Multifunctional Plasma Cured Cellulose Fibers Coated with Photo-Induced Nanocomposite toward Self-Cleaning and Antibacterial Textiles

Multifunctional fibrous surfaces with ultraviolet protection, self-cleaning, or antibacterial activity have been highly attractive. Nanocomposites consisting of silver (AgNPs) and titanium dioxide (TiO2 NPs) nanoparticles (Ag/TiO2) were developed and coated onto the surface of viscose fibers employing a straightforward pad–dry–cure procedure. The morphologies and elemental compositions were evaluated by scan electron microscopy (SEM), infrared spectra (FTIR), and energy-dispersion X-ray spectra (EDS). The resultant multifunctional textile materials displayed antibacterial and photo-induced catalytic properties. The photocatalyzed self-cleaning properties were investigated employing the photochemical decay of methylthioninium chloride, whereas the antibacterial properties were studied versus E. coli. The viscose fibers coated with Ag/TiO2 nanocomposite demonstrated improved efficiency compared with viscose fibers coated with pure anatase TiO2 nano-scaled particles

Polyaspartate-Ionene/Na+-Montmorillonite Nanocomposites as Novel Adsorbent for Anionic Dye; Effect of Ionene Structure

Surface modification of sodium montmorillonite (Na+-Mt) was performed using antimicrobial agents to produce an ecofriendly nanocomposite. The adsorption performance of the nanocomposite has been evaluated for the removal of Acid Blue 25 dye (AB25) as a model organic pollutant from wastewater. Sodium montmorillonite (Na+-Mt) was modified with three different ionene compounds through ion exchange, and further modified through reaction with polyaspartate to provide three ecofriendly nanocomposites (denoted ICP-1–3). The nanocomposites were characterized using FTIR, PXRD, TEM, SEM, and BET surface area. The adsorption isotherm of AB25 onto ICP-1, ICP-2 and ICP-3 was analyzed using the Langmuir, Freundlich, and Dubinin–Radushkevich (D–R) models. The adsorption isotherm was found to be best fitted by a Freundlich model. The thermodynamic parameters were calculated. The kinetics of the adsorption data were analyzed and the adsorption behavior was found to obey pseudo-second-order kinetics, and the intraparticle diffusion model. The adsorption mechanism was studied by FTIR

Enhancing the Antifungal Activity of Griseofulvin by Incorporation a Green Biopolymer-Based Nanocomposite

Fungal biofilms have caused several medical problems, resulting in significant morbidity and mortality as well as poor response to antifungal drugs. The current study was designed to evaluate the enhancement of antifungal and anti-biofilm activity of Griseofulvin-loaded green nanocomposite-based biopolymers (Ge-Nco) of glycogen and gelatin against different strains of pathogenic Candida species. The prepared Ge-Nco was characterized using Fourier-transform infrared (FT-IR), X-ray diffraction pattern (XRD), scanning electron microscopy-energy dispersive X-ray (SEM-EDX) and transmission electron microscope (TEM). In addition, the morphology of the mature biofilm and the inhibition of biofilm was monitored and visualized using confocal laser scanning microscopy (CLSM). The minimal inhibitory concentrations (MIC) and (IC50) of Griseofulvin alone and the prepared Ge-Nco against three different strains of Candida sp. were determined according to Clinical and Laboratory Standards Institute (CLSI) method. The effects of Griseofulvin alone and Ge-Nco on the tested Candida sp. biofilm formation were determined by the crystal-violet staining protocol. The biofilm inhibition potential of Ge-Nco against the tested Candida sp. was detected and depicted under CLSM (2.5 D view). The findings depicted that Ge-Nco was prepared in nanometer size (10–23 nm). The observed minimum inhibitory concentration (MIC) of Griseofulvin alone and Ge-Nco against three different Candida sp. were found to be in range 49.9–99.8 μg/mL and 6.24–12.48 μg/mL, respectively. These results provide evidence for implementing efficient antivirulence approaches against three different Candida sp. that would be less likely to foster the emergence of resistance

Facile Preparation of Porous Carbon Flake-Supported Nickel Nanoplates as Effective Catalysts for Methanol Electrooxidation

Herein, we report a facile and efficient method for fabricating porous carbon flakes (PCFs)-supported nickel nanoplates (Ni NPs) as electrocatalysts for methanol oxidation in alkaline media. The catalyst was fabricated in one step using molten salt synthesis. Various techniques were used to characterize the morphology and composition of the Ni NPs@PCFs catalyst, and these revealed that the Ni NPs were dispersed finely across the PCFs with a highly crystalline structure. The Ni NPs@PCFs catalyst demonstrated high electrocatalytic activity for methanol oxidation (121 mA/cm2 vs. Ag/AgCl), and it had an onset potential of 0.35 V. It also exhibited high stability in an alkaline electrolyte for the duration of the experiment (up to 2000 s)

The Impact of AN Contribution on the Thermal Characteristics and Molecular Dynamics of Novel Acrylonitrile–Styrene–Styrene Sodium Sulfonate Terpolymers

We performed a free radical solution polymerization of new acrylonitrile (AN), styrene (St) and styrene sodium sulfonate (SSS) acceptor–donor acceptor monomer systems. The compositions and structures of the produced terpolymers were elucidated using CHNS elemental analysis, and Fourier transform infrared (FTIR) spectroscopies. Three terpolymers candidates were chosen for detailed thermal investigations, where the AN molar ratio varied almost threefold (from ~6.9% to ~17.4%) while the molar ratios of St and SSS varied slightly, at average values around 76.0% and 12.9%, respectively. The glass transition (Tg) values of the terpolymers were measured calorimetrically. In addition, thermal gravimetric analyses (TGA) of the samples were conducted in the temperature range from room temperature to 800 °C. All terpolymers exhibited a single Tg value, indicating random copolymerization of the monomeric species. TGA results revealed that variation of the AN molar ratio had a significant influence on the thermal stabilities of the terpolymers. The impact of AN contribution on the molecular dynamics of the glass transition in the terpolymers was explained quantitatively in a framework of a molecular model

The Impact of AN Contribution on the Thermal Characteristics and Molecular Dynamics of Novel Acrylonitrile–Styrene–Styrene Sodium Sulfonate Terpolymers

We performed a free radical solution polymerization of new acrylonitrile (AN), styrene (St) and styrene sodium sulfonate (SSS) acceptor–donor acceptor monomer systems. The compositions and structures of the produced terpolymers were elucidated using CHNS elemental analysis, and Fourier transform infrared (FTIR) spectroscopies. Three terpolymers candidates were chosen for detailed thermal investigations, where the AN molar ratio varied almost threefold (from ~6.9% to ~17.4%) while the molar ratios of St and SSS varied slightly, at average values around 76.0% and 12.9%, respectively. The glass transition (Tg) values of the terpolymers were measured calorimetrically. In addition, thermal gravimetric analyses (TGA) of the samples were conducted in the temperature range from room temperature to 800 °C. All terpolymers exhibited a single Tg value, indicating random copolymerization of the monomeric species. TGA results revealed that variation of the AN molar ratio had a significant influence on the thermal stabilities of the terpolymers. The impact of AN contribution on the molecular dynamics of the glass transition in the terpolymers was explained quantitatively in a framework of a molecular model

A coupled catalyst composed of CoFe2O4 magnetic nanoparticle and [HMIM]Br-FeCl3 to intensify the oxidative desulfurization of FCC diesel

Ionic liquids have been extensively studied as solvents or catalysts for oxidative desulfurization (ODS) of diesel fuel, but it is still a challenge to reduce the desulfurization time and steps. In this work, a new highly efficient desulfurization system composed of CoFe2O4 magnetic nanoparticle, [HMIM]Br-FeCl3 and H2O2 was developed for the ODS of FCC diesel fuel. The desulfurization performances were investigated including desulfurization time, temperature, volume ratio of IL/oil, O/S molar ratio, dosage of CoFe2O4, FeCl3 content in ILs, regeneration, and reuse of catalyst and solvent. Owing to the coupled catalytic roles of CoFe2O4 magnetic nanoparticle and [HMIM]Br-FeCl3, where Co2+ and Fe3+ interact with H2O2 to produce •OH radical that converts S-compounds into sulfone and sulfoxide compounds, such a desulfurization system is highly effective in removing S-compound in diesel fuel. The S-content in FCC diesel fuel was reduced from the original 272.8 ppm to 0.5 ppm with 99.82% S-removal efficiency after one step within 8 min under the optimal conditions of 25 °C, 8 min, V(IL/oil) = 1:10, O/S = 20, 5 wt% CoFe2O4 dosage and n([HMIM]Br)/n(FeCl3) = 1:1; the desulfurization performance is much better in desulfurization time and steps than other desulfurization systems reported previously. The desulfurization system can be regenerated and reused without remarkable loss of desulfurization activity. A desulfurization mechanism was proposed