Dye removal membrane from electrospun nanofibers of blended polybutylenesuccinate and sulphonated expanded polystyrene waste.

Polystyrene (PS) is a thermoplastic polymer used in food packaging and the manufacture of trays and cups, among other applications. In this work, the preparation of a membrane by electrospinning blended sulphonated expanded PS waste and polybutylenesuccinate (PBS) is described. The fiber quality is controlled by selecting the right polymers' ratios and solvents. Investigation of the structure of the produced membranes by Fourier transform infrared spectroscopy-attenuated total reflectance confirmed the successful sulphonation of expanded PS and the appearance of characteristic (PBS) bands in the prepared blends. Morphology study of the electrospun membranes using a scanning electron microscope revealed that the quality of the fibers is improved significantly by increasing the amount of PBS in the blend solution. Moreover, continuous and more homogenous fibers are produced by increasing the ratio of PBS to 2%. The efficiency of the prepared membranes in dye removal was tested using methylene blue. The effects of different parameters such as, pH, contact time, temperature, and dye concentration have been studied. Also, kinetic and adsorption isotherm models as well as the durability of the prepared membranes were investigated. The membrane prepared from PSS/1% PBS demonstrated the highest dye uptake (846 mol) with good regeneration efficiency. The adsorption process was found to be endothermic and fits the Freundlich isotherm and pseudo-second-order kinetic model. The values of activation energy for the adsorption process are 36.98, 30.70, and 43.40 kJ/mol over PSS, PSS/1% PBS and PSS/2% PBS, respectively.

Charge transport and heavy metal removal efficacy of graphitic carbon nitride doped with CeO2.

Doping of graphitic carbon nitride (g-C3N4) with semiconductors prevents electron-hole recombination and enhances adsorption capacity. This work investigates the synthesis of a water remediation material using g-C3N4 doped with CeO2 using two different techniques. The chemical structures of the doped g-C3N4 samples were confirmed using FTIR, XRD, XPS and their morphology was studied using SEM-EDX. Charge transport through the doped materials was illustrated by a comprehensive dielectric study using broadband spectroscopy. The ability of doped g-C3N4 to adsorb heavy metals was investigated thoroughly in the light of applying different parameters such as temperature, pH, time, and concentration. The results showed that the mode of doping of g-C3N4 by CeO2 strongly affected its adsorption capacity. However, g-C3N4 doped with CeO2 using the first mode adsorbed 998.4 mg g-1 in case of Pb2+ and 448 for Cd2+. Kinetic study revealed that the adsorption process obeyed PSORE as its q exp e is close to its q cal e and the rate-controlling step involved coordination among the synthetic materials and the heavy metal ions. The recovery of Pb2+ and Cd2+ ions from various sorbents was investigated by utilizing different molar concentrations of HNO3 and indicated no significant change in the sorption capability after three different runs. This study has demonstrated an efficient method to obtain a highly efficient adsorbent for removing heavy metals from waste water.

Photoluminescent and photochromic smart window from recycled polyester reinforced with cellulose nanocrystals.

Smart windows with long-persistent phosphorescence, ultraviolet (UV) light protection, high transparency, and high rigidity were developed by easily immobilizing varying ratios of lanthanide-activated aluminate phosphor nanoscale particles within a composite of recycled polyester/cellulose nanocrystals (RPET/CNC). Cellulose nanocrystals were prepared from rice straw waste. Cellulose nanocrystals were used at low concentration as both crosslinker and drier to improve both transparency and hardness. The phosphor nanoscale particles must be distributed into the recycled polyester/cellulose nanocrystals composite bulk without agglomeration to produce transparent RPET/CNC substrates. Photoluminescence characteristics were also studied using spectroscopic profiles of excitation/emission and decay/lifetime. The hardness efficiency was also examined. This transparent recycled polyester waste/cellulose nanocrystals nanocomposite smart window has been shown to change colour under UV light to strong green and to greenish-yellow when it is dark, as proved by Commission Internationale de l'éclairage (CIE) laboratory colour parameters. It was found that the afterglow RPET/CNC smart window had phosphorescence intensities of 428, 493, and 523 nm upon excitation at 368 nm. There was evidence of improved UV shielding, photostability, and hydrophobic activity. In the presence of a low phosphor ratio, the luminescent RPET/CNC substrates showed quick and reversible fluorescence photochromic activity when exposed to UV radiation.

Synergistic effect of zinc oxide nanorods on the photocatalytic performance and the biological activity of graphene nano sheets.

In this work, decoration of the graphene surface with 5 wt. % ZnO nanorods (ZnO NRs), to ensure the potential photocatalytic performance of the formed nanocomposites, is demonstrated. Graphene oxide (GO) was synthesized with Hummer method followed by reduction to give reduced graphene oxide (RGO). The adjustable nano-compositing exhibited long-sought workability not only in in-situ incorporation of nanorods while reduction of graphene oxide (IZG) but also in ex-situ mixing of RGO or GO with the nanorods, (EZG) and (ZGO) respectively. The demineralization of synthetic wastewater has been evaluated by chemical oxygen demand and the obtained nanocomposites possess enhanced photocatalytic activities with 30 % and 35% over pure RGO and GO, respectively. This higher efficiency could be attributed to the synergistic effect between ZnO and the planner structure of graphene sheets which developed unprecedented polycrystalline structure. Also, the results proved that even the RGO or GO have played a dual function in photocatalysis, adsorption, and degradation. Also, the bactericidal effect of the prepared samples was studied against deleterious microorganisms. The findings of this work pave the way for the new generation of highly efficient photocatalysts based graphene with economic attraction and environmental impact.

Photocatalytic activity and antimicrobial properties of paper sheets modified with TiO2/Sodium alginate nanocomposites.

Photocatalytic paper sheets were prepared by addition of different ratios of TiO2/Sodium alginate (TSA) nanocomposite. The modified paper sheets were characterized by XRD, TGA. Their morphology was studied by scanning electron microscope (SEM) and energy dispersive X-ray (EDX). Photocatalytic activity of modified paper has been studied by analysis of chemical oxygen demand (COD) of waste-water. The results confirmed the mineralization of the waste-water and enhanced removal of chemical oxygen demand (COD) by increasing the amount of photocatalyst in the paper. Moreover, the results also confirmed that presence of sodium alginate as biopolymer increased adhesion of nanoparticles to paper fibers and reduced the harmful effect of the photocatalyst on them. The paper sheets containing 7% as well as 15% TSA showed high photocatalytic activity and anti-bacterial effect against Salmonella typhimurium higher than standard antibiotic beside other microorganisms such as Candida albicans. The maximum antimicrobial effect was found in case of specimen loaded with 15% TSA. Moreover, it was found that by adding 20% TSA to the paper matrix, the properties of the paper composite collapse. The obtained results confirm the possible utilization of the modified paper in both hygienic and food packaging applications.