A flame-retardant composite was synthesized through a simple graphene oxide functionalization route with hexachlorocyclotriphosphazene and p-phenylenediamine. Flame experiments conducted on the synthesized composite proved its importance as tremendously resistant to fire. The thermogravimetric analysis (TGA) shows clearly that the functionalized graphene oxide (FGO) exhibits an enhanced thermal stability and better temperature resistance. A thermoset epoxy resin was prepared by incorporating different percentages (2, 5, and 10%) of FGO to diglycidyl ether of bisphenol A (DGEBA). The flame-retardant properties, thermal degradation behavior, and combustion of the DGEBA thermosets cured by m-phenylenediamine were investigated using a Bunsen burner flame approaching the flame temperature of a fire and TGA. The chemical structure of FGO was characterized with spectroscopic and imaging techniques including Fourier transform infrared spectroscopy, Raman spectroscopy, X-ray diffraction, TGA, scanning electron microscopy, energy-dispersive X-ray spectroscopy elemental mapping, and X-ray photoelectron spectroscopy. Due to its high flame-retardant capabilities, such a composite could promise potential applications in the manufacture of inflammable materials for different uses.

Three-dimensional (3D) reduced graphene oxide (rGO) modified by polyethyleneimine (PEI) was prepared and functionalized by fluorophore-labeled dexamethasone-aptamer (Flu-DEX-apt) via π–π stacking interaction. The rGO/PEI/Flu-DEX-apt was used as a selective membrane for dexamethasone hormone removal from water. The prepared rGO/PEI/Flu-DEX-apt membranes were stable, insoluble, and easily removable from liquid media. The membrane was characterized by Raman spectroscopy, scanning electron spectroscopy, and FTIR spectroscopy. The rGO/PEI/Flu-DEX-apt membrane showed high sensitivity and specificity toward the dexamethasone hormone in the presence of other steroid hormone analogs, such as progesterone, estrone, estradiol, and 19-norethindrone. The fluorescence and UV–visible spectroscopy were used to confirm the membranes performance and the quantification of hormones removal. The resulting data clearly show that the graphene oxide concentration influence the aptamers and analytes interaction (π–π stacking interaction). It was found that by varying the graphene oxide concentration yields to different porosities of rGO/PEI/Flu-DEX-apt membranes affects the adsorption recovery rate, as well as the specificity and selectivity toward the dexamethasone hormone.

The extensive use of the herbicide glyphosate has raised several health concerns due to the known toxicity of this chemical. The existing methods for glyphosate detection need better and more rapid accessibility for quick detection in an efficient manner. Here, we report an ultrasensitive aptamer-based electrochemical detection method for glyphosate. A high affinity single-stranded DNA (ssDNA) that binds specifically to glyphosate (GlyP) was selected and identified in vitro by the method of systemic evolution of ligands by exponential enrichment (SELEX) assisted by graphene oxide (GO), GO-SELEX. After eight GO-SELEX cycles, the ssDNA was sequenced, and the obtained aptamers were subjected to binding assays to evaluate their affinity and specificity to GlyP. The inherent GlyP–aptamer interaction was investigated by circular dichroism spectroscopy (CD). The selected sequence, denominated GlyP_1, exhibited a low dissociation constant (K d) of 30.73 ± 1.25 nM and excellent selectivity for glyphosate. Prior to gold electrode modification, GlyP_1 was functionalized by the disulfide label and used as a recognition element for glyphosate detection. The surface modification steps for the gold electrodes to develop the aptasensor were followed up by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) in the presence of a redox probe, [Fe­(CN)6]3–/4–. The resulting aptasensor demonstrated an operation range from 1.16 pM to 400 pM, with a limit of detection (LOD) of 1.16 pM. Thus, in this work we report an effective sensing method that could provide a potential alternative to traditional analyses techniques for quick and easy monitoring of glyphosate in food and water.

Highly cross-linked inorganic and organic hybrid cyclomatrix-polyphosphazenes microspheres (C-PPZs) have been successfully synthesized by a one-pot polymerization technique between hexachlorocyclotriphosphazene and p-phenylenediamine in the presence of triethylamine (TEA), and they were used for enhancing the flame retardancy of epoxy resins (EPs). A thermoset EP was prepared by incorporating different percentages (2, 5, and 10%) of C-PPZs into diglycidyl ether of bisphenol A (DGEBA). The results reveal that the size and morphology of the microspheres can be tuned by varying the synthesis temperature. The average size of C-CPPZs gradually increased from 3.1, 4.9, to 7.8 μm as the temperature was increased from 100, 120, to 200 °C, respectively. The thermogravimetric analysis showed that the C-CPPZ microspheres have good thermal stability up to 900 °C with about ∼10 wt % mass loss for C-CPPZs formed at 200 °C compared to ∼30 wt % mass loss for those obtained at 100 and 120 °C. The 10% loss at 900 °C is much lower than the previous research concerning the thermal stability of cyclophosphazene, in which more weight losses were observed at lower temperatures. The resulting C-CPPZ microspheres were characterized by spectroscopic and imaging techniques including Fourier transform infrared spectroscopy, Raman spectroscopy, X-ray diffraction, scanning electron microscopy, energy-dispersive X-ray spectroscopy, elemental mapping, and X-ray photoelectron spectroscopy.