Targeted elimination of molybdenum ions from a leaching solution with the ability of radiated grafting GMA-PAN nanofibers.

In this study, electrospun polyacrylonitrile nanofibers were effectively functionalized for enhanced molybdenum ion adsorption through a multi-step approach. Initially, glycidyl methacrylate was grafted onto the nanofibers via irradiation-induced grafting polymerization, followed by chemical modification with various amino groups, with triethylamine identified as the optimal modifier. The impacts of key synthesis parameters and reaction conditions on grafting level and adsorption capacity were thoroughly investigated, with a focus on achieving maximum efficiency. The resulting nanofibers were characterized using FTIR, SEM, and BET techniques, confirming the successful modification and structural features conducive to adsorption. Furthermore, a comprehensive experimental design, incorporating a central composite design, yielded optimal conditions for molybdenum adsorption, with key parameters including monomer concentration, irradiation dose, adsorbent mass, initial concentration, time, pH, temperature, and amine concentration. The adsorption kinetics were effectively described by the pseudo-second-order model, while the Langmuir isotherm model provided valuable insight into the adsorption behavior. Impressively, the adsorbent exhibited exceptional adsorption efficiency, surpassing 98% even after six adsorption-desorption cycles using 0.5 M HCl. Thermodynamic analysis revealed the exothermic nature of the adsorption process, along with decreased entropy and overall spontaneity, underlining the favorable conditions for molybdenum adsorption. Notably, the synthesized adsorbent demonstrated notable selectivity for molybdenum and achieved an impressive adsorption capacity of 109.79 mg/g, highlighting its potential for practical applications in molybdenum removal from aqueous solutions.

Investigation of the leaching behavior of Na and Si in simulated HLW borosilicate glass obtained from the waste of a 1000 MWe class PWR reactor: using the response surface method.

The immobilization of high-level nuclear waste (HLW) in glass waste matrices provides the key safety function of slowing down radionuclide emissions from an underground disposal site. This study examines the leaching behavior of two major elements, Na and Si, in HLW borosilicate glass simulated from waste of a 1000 MWe class pressurized water reactor (PWR) using response surface methodology and Box-Behnken Design. The design of the experiment was carried out considering three independent variables: the pH of the solution, the contact time, and the leaching temperature, leading to 17 leaching runs performed using the static product consistency test (PCT). The results of statistical analysis (ANOVA: analysis of variance) indicated that the effects of the individual variables and the interactions between them were statistically significant, and the relative consistency of the data further confirmed the model's applicability. Data obtained from the PCT experiments revealed that the leaching behavior of Na and Si in the evaluated waste glass exhibited similar behavior to previously researched glasses for each condition tested.

Iodine-131 radiolabeling of poly ethylene glycol-coated gold nanorods for in vivo imaging.

Gold nanorods (GNRs) can be used in various biomedical applications; however, very little is known about their in vivo tissue distribution by radiolabeling. Here, we have developed a rapid and simple method with high yield and without disturbing their optical properties for radiolabeling of gold rods with iodine-131 in order to track in vivo tissue uptake of GNRs after systemic administration by biodistribution analysis and γ-imaging. Following intravenous injection into rat, PEGylated GNRs have much longer blood circulation times.

Synthesis and characterization of new biopolymeric microcapsules containing DEHPA-TOPO extractants for separation of uranium from phosphoric acid solutions.

A novel microcapsule adsorbent for separation of uranium from phosphoric acid solutions was developed by immobilizing the di(2-ethylhexyl) phosphoric acid-trioctyl phosphine oxide extractants in the polymeric matrix of calcium alginate. Physical characterization of the microcapsules was accomplished by scanning electron microscopy and thermogravimetric techniques. Equilibrium experiments revealed that both ion exchange and solvent extraction mechanisms were involved in the adsorption of [Formula: see text] ions, but the latter prevailed in a wider range of acid concentration. According to the results of kinetics study, at low acidity level, the rate controlling step was slow chemical reaction of [Formula: see text] ions with the microdroplets of extractant, whereas it changed to intraparticle diffusion at higher acid concentration. The study also attempted identification of the diffusion paths of the ions within the microcapsules, and the mechanism of change of mass transfer rate during the uptake process. The prepared microcapsules preserved their entire capacity after three cycles of adsorption, and their breakthrough behaviour was well fitted by a new formula derived from shrinking core model.

Study on physico-mechanical and gamma-ray shielding characteristics of new ternary nanocomposites.

In this study, a series of "Epoxy-Clay-PbO" nanocomposites under the name of ECPNCs were prepared by the molding method, and their physico-mechanical properties were investigated by different techniques. Focus of the work, was on the shielding ability of the ECPNCs for the gamma rays, emitted from Ir-192, Cs-137 and Co-60 with a wide range of energy. Scanning electron microscopy, and X-ray diffractometry demonstrated that clay platelets were fully exfoliated, and the PbO particles were homogenously distributed in the polymeric matrix. Thermo-gravimetric analysis and standard tensile tests revealed that PbO content has an "increasing/decreasing" effect on "thermal stability/mechanical strength" of the nanocomposites. Gamma shielding experiments showed that efficacy of ECPNCs containing 30 wt% PbO was 47% better than that of concrete. Experimental attenuation data were confirmed by theoretical calculations, so that the maximum difference between them was 14.1%. Furthermore, a correlation was developed between PbO content of the ECPNCs and their mass attenuation coefficient for all gamma sources.

Fabrication of new magnetite-graphene nanocomposite and comparison of its laser-hyperthermia properties with conventionally prepared magnetite-graphene hybrid.

A single step supercritical method was introduced for synthesis of "magnetite - reduced graphene oxide (M-rGO)" composite in supercritical methanol. Modified surface, smaller size, lesser cytotoxicity, and homogenous dispersion of Fe3O4 nanoparticles on the graphene surface were advantages of this new M-rGO composite in comparison to the materials synthesized by conventional wet chemical method (M-GO). Nanocomposites were injected in tissue equivalent phantoms of agarose gel in 10mg/g dosage, and were irradiated by a 1600mW laser beam at wavelength of 800-810nm. The M-rGO and M-GO were found to be the most and the least efficient samples for increasing the temperature of the phantom. As for mathematical analysis of the heating process, a heat transfer model was developed and solved by the COMSOL Multiphysics software. Results showed an appreciable agreement with the experiments and revealed enhancement in thermal conductivity and light absorption coefficient of tissue by injecting of M-rGO sample. Our findings showed that M-rGO is a promising material for laser hyperthermia, which can deposit adequate heat dose with desirable effect in the tumorous cells in a short period.

Removal of heavy metals from aqueous solution using platinum nanopartcles/Zeolite-4A.

The effects of varying operating conditions on metals removal from aqueous solution using a novel platinum nanopartcles/Zeolite-4A adsorbent are reported in this paper. Characterization of the adsorbent showed successful production of platinum nanopartcles on Zeolite-4A using 3 Wt% platinum. The effects of operation conditions on metals removal using this adsorbent were investigated. The optimal metals adsorption was observed at pH 7, 0.1 g/10 mL dosage and 30 min contact time. Sorption data have been interpreted in terms of Langmuir and Freundlich isotherms.

Preparation of stable alginate microcapsules coated with chitosan or polyethyleneimine for extraction of heavy metal ions.

Stable alginate microcapsules in dried form containing bis(2,4,4-trimethylpentyl) monothiophosphinic acid (HA) were prepared by coating of fresh alginate microcapsules with chitosan or polyethyleneimine (PEI). The thickness of coatings was estimated by electron probe microanalysis (EPMA), along with electron microscopy (SEM), as well as comparison of uptake percentage of coated and uncoated hollow capsules. Characterization of microcapsules was carried out by Ag(+) uptake experiments, destructive chemical analyses and thermogravimetric methods (TG and DTA). Chemical stability tests in HNO(3) and NaNO(3) media indicated that the coating with 4-double layer chitosan or mono-layer PEI led to an appreciable enhancement of impermeability in the range of pH > 1 or [Na(+)] < 1 M (mol dm(-3)). Unfortunately, multiple coating causes some extractant losses due to effect of physical stress during the coating; however, PEI-coated microcapsules nearly completely hold their extractant content. Stable extractive microcapsules have an appreciable potential for the selective removal of heavy metal ions.