Crosslinked Polydiallyldimethylammonium Chloride Adsorbent for the Selective Separation of Rhenium Ions from Pregnant Leach Solutions.

The depletion of valuable mineral reserves has rendered effluents generated from mining and industrial processing activities a promising resource for the production of precious elements. The synthesis and improvement of new adsorbents to extract valuable compounds from industrial wastes and pregnant leach solutions, besides increasing wealth, can play a significant role in reducing environmental concerns. In this work, a new and low-cost adsorbent for the selective extraction of rhenium (perrhenate ions, ReO4-) was synthesized by the free-radical polymerization (FRP) of a diallyl dimethylammonium chloride monomer (quaternary amine) in the presence of a crosslinker. Various methods were employed to characterize the polymeric adsorbent. The results revealed that the designed polymeric adsorbent had a high surface area and pores with nano-metric dimensions and a pore volume of 6.4 × 10-3 cm3/g. Four environments-single, binary, multicomponent, and real solutions-were applied to evaluate the adsorbent's performance in the selective separation of Re. Additionally, these environments were used to understand the behavior of molybdenum ions, the primary competitors of perrhenate ions in the ion exchange process. In competitive conditions, using variations in qe,mix/qe, an antagonism phenomenon (qe,mix/qe < 1) occurred due to the inhibitory effect of surface-adsorbed molybdenum ions on the binding of the perrhenate ions. However, across all conditions, the separation values for Re were higher than those for the other studied elements (Mo, Cu, Fe).

Preparation of an innovative series of respiratory nano-filters using polystyrene fibrous films containing KCC-1 dendrimer and ZnO nanostructures for environmental assessment of SO2, NO2 and CO2.

Air pollution has become a major challenge that threatens human health. The use of respiratory filters is one of the proposed solutions. In this study, using polystyrene (PS) fibers and various nanomaterials, improved respiratory filters were fabricated to remove air pollutants. In this context, ZnO nanoparticles (ZnO NPs) integrated into dendritic structures of KCC-1 silica were used to improve the filters' ability to absorb pollutants. For the first time, the removal of gasses by modified filters with a novel polymeric nanocomposite (PS/ZnO-KCC-1) stabilized on the surface of respiratory filters was investigated. Moreover, two different methods including stabilized- and solution-based techniques were used to prepare the filters with different amounts of ZnO NPs and their efficiency was evaluated. All synthesized nanocomposites and developed filters were characterized by FT-IR, FESEM, TGA and XRD methods. The successful stabilization of nanostructures on the fibers was proved and the performance of the fibers was investigated with some tests, such as pressure drop and removal of suspended particles and CO2 (89%), NO2 (86%), and SO2 (83%) gases. PS/KCC-1-ZnO (5%) has better performance than other prepared fibers. The results showed that the removal of suspended particles in the filter containing ZnO and KCC-1 (M5) nanostructures was improved by 18% compared to the filter consisting of polystyrene fibers. The pressure drop increased with the addition of nanostructures and reached 180 Pa in the M5 filter. The filter containing ZnO NPs showed antibacterial activity against Staphylococcus (S.) aureus and Escherichia (E.) coli as Gram-positive and Gram-negative model bacteria using the Agar disk-diffusion method. Based on the results, the use of improved respiratory filters is recommended as an effective solution for combating air pollution and protecting human health.

Accelerated synthesis of 1,8-dioxo-octahydroxanthene and 1,8-dioxo-decahydroacridine derivatives using dendritic mesoporous nanosilica functionalized by hexamethylenetetramine: a novel nanocatalyst.

Xanthene and acridine derivatives are interesting organic compounds that are used in different research fields like biomedicine and pharmaceutical science. However, applied catalysts for their synthesis have some limitations such as long reaction times, the need for harsh conditions and low yield. So, discovery of novel catalysts for the synthesis of xanthene and acridine derivatives is highly demanded. To overcome the limitation of previous methods on the efficient synthesis of 1,8-dioxo-octahydroxanthene and 1,8-dioxo-decahydroacridine derivatives, a green heterogeneous organic nano-catalyst (Cu@KCC-1-nPr-HMTA) was synthesized by covalent attachment of hexamethylenetetramine to the cavities and channels of dendritic mesoporous nanosilica (KCC-1). The prepared nano-catalyst was identified using various spectroscopic and microscopic methods including scanning electron microscopy (SEM), Fourier transform infrared (FT-IR), X-ray energy diffraction (EDX), EDX mapping and nitrogen adsorption-desorption analysis (BET-BJH). The prepared green nano-catalyst showed a spherical and dendritic structure with a surface area of 65.699 m2 g-1, average pore size of 40.78 nm and pore volume of 0.66 cm3 g-1. Also, Cu@KCC-1-nPr-HMTA has many chemo-active sites for the condensation reaction and was used as an efficient nano-catalyst towards one-step synthesis of 1,8-dioxo-decahydroacridine and 1,8-dioxo-octahydroxanthene derivatives from the reaction of aromatic aldehydes, dimedone, and ammonium acetate under solvent-free conditions. Short reaction times of 1 to 5 minutes for 1,8-dioxo-decahydroacridine and 30 to 55 minutes for 1,8-dioxo-octahydroxanthene derivatives, high yields and mild reaction conditions are advantages of the proposed synthetic method. It is hoped that the engineered nano-catalyst will be used for the synthesis of other organic compounds in the future.

Attenuation properties of hybrid nanocomposite film containing Ce2O, GO, and α-Al2O3 nanoparticles for high energy radiations.

The use of diagnostic radiation in medical centers has spread due to the incidence of various diseases. Thus, it is essential that patients and medical staff wear protective clothing to protect themselves from their harmful effects. In the past, lead protective clothing has been used; however, the toxicity and heaviness of lead have limited the tendency to use these clothing. Recently, nanocomposites containing heavy element nanoparticles have been introduced as an alternative to lead coatings. In this study, hybrid nanocomposites containing ceria (CeO2), alumina (Al2O3), and graphene oxide (GO) nanoparticles were studied for this purpose. Ceria, alumina, and graphene oxide nanoparticles were mixed with polyethylenevinylacetate (EVA) dissolved in chloroform and casted on a glass plate to form nanocomposite films. The prepared nanoparticles and films were characterized by Fourier Transform Infrared Spectroscopy, Field Emission Scanning Electron Microscope, Thermal Gravimetric Analysis, and Energy Dispersive X-ray Analysis, and then the attenuation properties of the films against high-energy radiation (120 kV) were studied in two narrow and broad beam geometries. The results showed that hybrid films, despite having a lower percentage of nanoparticles, showed better attenuation properties, which indicated the synergistic effect of nanoparticles with different mechanisms in attenuating the radiations. The attenuation ability of these films was considerable due to their lower density compared to lead. The fabricated hybrid nanocomposite films with a suitable performance in attenuation of high-energy radiations used in therapeutic diagnostics, can be proposed as a suitable alternative to conventional lead clothing.

An electrochemical sensor for the detection of arsenic using nanocomposite-modified electrode.

The aim of this research is to develop an electrochemical sensor based on a conducting polymer, polyaniline, and a cationic polymer, poly(diallyldimethylammonium chloride), reinforced with graphene oxide nanosheets functionalized with acrylic acid. The two-dimensional nature of acrylic acid functionalized graphene oxide nanosheets and clusters made of conductive polymers and acrylic acid functionalized graphene oxide nanosheets were confirmed by microscopic tests. The prepared nanocomposite was deposited on the glassy carbon electrode in order to prepare an electrochemical sensor for the detection of arsenic by cyclic voltammetry and differential pulse voltammetry methods. It should be mentioned that the presence of acrylic acid functionalized graphene oxide nanosheets increases the surface area due to the nano size effect and better dispersion of this nanomaterial, poly(diallyldimethylammonium chloride), increases the adsorption capacity of the analyte due to electrostatic interaction between the negatively charged analyte and positively charged surface, and polyanilin increases the charge transfer rate due to the good conductivity. The results show that the prepared electrode has a sensitivity equal to 1.79 A/M with 0.12 µM as the detection limit. The proposed sensor could be used for the determination of total inorganic arsenic by first oxidative pretreatment for conversion of As(III) to As(V).

Utilization of a mixed matrix membrane modified by novel dendritic fibrous nanosilica (KCC-1-NH-CS2) toward water purification.

Various nanostructures have been used to improve the performance of nanocomposite membranes. Dendritic fibrous nanosilica (DNFS) is a new nanostructure and its performance as an adsorbent for the removal of pigments has been investigated. In this study, a type of modified dendritic fibrous nanosilica containing CS2 groups (KCC-1-NH-CS2) was synthesized and inserted as an additive into nanocomposite acrylonitrile-butadiene-styrene (ABS) membranes. Due to its high surface area and unique functional groups, this additive can improve the membrane's ability to remove dyes from aqueous media. Synthesized nanostructures and membranes were characterized by different analysis. The results showed that the water contact angle as a measure of surface hydrophilicity in membrane M5 compared to membrane M1 decreased from 79° to 67°. Water absorption (swelling degree) in membrane M5 increased by more than 100% compared to the bare membrane. Also, this membrane, despite having high porosity (42%) and improved flux (35 L m-2 h-1), has a better efficiency in removing dyes (MG: 99%, MB: 98%, MO: 82%) in comparison with other reported works.

Fabrication of chitosan-based electrospun nanofiber scaffold: Amplification of biomechanical properties, structural stability, and seeded cell viability.

The cell scaffolds should structurally be manufactured similar to the target tissue's extracellular matrix. This property should be maintained until cell differentiation. For this purpose, in the current study, electrospun nanofiber (EN) of chitosan (Ch)/polyvinyl alcohol (PVA), as a tissue-friend scaffold, was fabricated by electrospinning in different formulations and borax was utilized as an innovative cross-linking agent to up-regulate the structural and biomechanical properties. The weight loss, water absorbability, structural stability, tensile strength and biocompatibility of borax-included and non-included ENs were compared. The finest morphology, weight loss, water absorbability, structural stability in an aqueous environment, tensile strength and cell viability were found in the borax-included EN containing Ch50.00%v/PVA50.00%v. Moreover, The ENs exhibited appropriate antibacterial properties against Gram-positive and Gram-negative bacteria. In conclusion, borax can be used to improve the mechanical and biocompatibility features of the Ch/PVA-based ENs. Furthermore, it could be suggested that borax-included Ch/PVA ENs can exhibit high appropriate biological properties, candidate them as an appropriate scaffold in the field of tissue engineering. However, in vivo trials are needed to clearly their side effects and advantages.

Preparation and investigation of poly(methylmethacrylate) nano-capsules containing haloxyfop-R-methyl and their release behavior.

In this study, the preparation and characterization of haloxyfop-R-methyl herbicide loaded in poly(methylmethacrylate) (PMMA) nano-capsules by emulsion polymerization and its release behavior were investigated. The chemical characterizations of PMMA/haloxyfop-R-methyl nano-capsules were confirmed by FT-IR spectroscopy method, and the surface morphology was studied by field emission scanning electron microscopy and transmission electron microscopy. Also, the herbicide loading and encapsulation efficiency were analyzed for the herbicide-loaded nano-capsules. The release rate of PMMA/haloxyfop-R-methyl nano-capsules was determined by UV-visible spectroscopy. The thermal properties and thermal stability of nano-capsules were explored by the thermal gravimetric analysis method. The diameter of the nano-capsules was in the range of 100-300 nm. Increasing the amount of herbicide in nano-formulations significantly affected the surface of the nano-capsules and reduced their surface smoothness. Triton-X100 was identified as the best surfactant for the preparation of nano-capsules, and the sample containing the lowest herbicide content showed the best performance in terms of encapsulation and loading efficiency. This sample showed a steady-state release rate during the six days.