Commercial epoxy resin loaded with phosphorus flame retardant led to composites exhibiting remarkable improved flame retardancy and thermal stability.

Advanced flame retardant epoxy resins, environmentally friendly, with different contents of a new oligophosphonate (PFR), were prepared using dicyandiamide as a hardener and 1,1-dimethyl-3-phenylurea as an accelerator. PFR, with a high phosphorus content, was synthesized by polycondensation reaction of phenylphosphonic dichloride with a phosphorus-containing bisphenol, namely bis((6-oxido-6H-dibenz[c,e][1,2]oxaphosphorinyl)-(4-hydroxyaniline)methylene)-1,4-phenylene. The bisphenol was prepared by reacting 9,10-dihydro-oxa-10-phosphaphenanthrene-10-oxide with an imine bisphenol resulting from the condensation of 4-aminophenol with terephthalaldehyde. The structure and morphology of cured epoxy resins were evaluated by Fourier transform infrared spectroscopy and scanning electron microscopy (SEM) analysis, respectively. Differential scanning calorimetry analysis revealed that cured epoxy resins containing PFR possessed slightly higher glass transition temperatures than phosphorus-free cured epoxy resin. Thermogravimetric analysis and limiting oxygen index values indicated that the incorporation of PFR into epoxy resin substantially enhanced the thermal stability and flame retardancy of the char layer at high temperature. The surface morphology of the char residue was studied by SEM measurements. The kinetic processing of thermogravimetric data was carried out using Friedman and Vyazovkin methods. The lifetime prediction analysis established that the fire-resistant phosphorus-containing epoxy resins could be used at a constant temperature of 200 °C up to 620–630 minutes. The new PFR can be successfully used as a very efficient flame retardant for improving the fire-resistance properties of epoxy resins.

The current study focuses on the application of cytotoxicity tests upon one membrane matrix based on electrospun polyimide fibers, appealing for biomedical application, such as scaffolds for cell growth, patches or meshes for wound healing, etc. Assays were performed in order to determine the viability and proliferation of L929 murine fibroblasts after they were kept in direct contact with the studied electrospun polyimide fibers. Increased cell viability and proliferation were detected for cells seeded on electrospun polyimide fibers membrane, in comparison with the control system, either after two or six days of evaluation. The number of live cells was higher on the studied material compared to the control, after two and six days of cell seeding. The tendency of the cells to proliferate on the electrospun polyimide fibers was revealed by confocal microscopy. The morphological stability of electrospun polyimide membrane was evaluated by SEM observation, after immersion of the samples in phosphate buffer saline solution (PBS, 7.4 at 37 °C) at various time intervals. Additionally, the easy production of electrospun polyimide fibers can facilitate the development of these types of matrices into specific biomedical applications in the future.