No abstract

Polyethylene (PE) is one the most used plastics worldwide for a wide range of applications due to its good mechanical and chemical resistance, low density, cost efficiency, ease of processability, non-reactivity, low toxicity, good electric insulation, and good functionality. However, its high flammability and rapid flame spread pose dangers for certain applications. Therefore, different flame-retardant (FR) additives are incorporated into PE to increase its flame retardancy. In this review article, research papers from the past 10 years on the flame retardancy of PE systems are comprehensively reviewed and classified based on the additive sources. The FR additives are classified in well-known FR families, including phosphorous, melamine, nitrogen, inorganic hydroxides, boron, and silicon. The mechanism of fire retardance in each family is pinpointed. In addition to the efficiency of each FR in increasing the flame retardancy, its impact on the mechanical properties of the PE system is also discussed. Most of the FRs can decrease the heat release rate (HRR) of the PE products and simultaneously maintains the mechanical properties in appropriate ratios. Based on the literature, inorganic hydroxide seems to be used more in PE systems compared to other families. Finally, the role of nanotechnology for more efficient FR-PE systems is discussed and recommendations are given on implementing strategies that could help incorporate flame retardancy in the circular economy model.

The ORCID identification number(s) for the author(s) of this article can be found under https://doi.org/10.1002/mame.201700570. Sulfated Zirconia FillersThis study expresses that the characteristics of sulfated zirconia (SZ) nanostructure in sulfonated poly(ether ether ketone) (SPEEK)-based membranes is the key to optimize their properties for fuel cell applications. Two types of SZ treating in different thermal conditions are produced by precipitation and analyzed by X-ray diffraction, thermogravimetric analysis, Fourier transform infrared spectroscopy, energy-dispersive X-ray analysis, and transmission electron microscopy. Sulfate concentration on both types of SZ is changing from 0.54 to 1.45 wt% and thus the SZ samples differ in particle size and sulfate content. The nanocomposite membranes are prepared by incorporating 6 wt% of SZ samples into SPEEK matrix in casting procedure followed by performing electrochemical characterizations and impedance spectroscopy. Moreover, morphology, mechanical, and chemical stability of the membranes are investigated by field emission scanning electron microscopy, stress-strain, and ex situ Fenton's tests. The incorporation of SZ sample having more surface sulfate groups in the SPEEK matrix results in not only excessive oxidative stability and tensile strength but also more acidic sites for ion transport, promoting conductivity. Furthermore, both types of nanocomposite membranes show improved ionic conductivity and water affinity with a lower tendency to swell rather than the plain SPEEK membrane. It is proved that desired consequences of doping SZ into SPEEK matrix can be intensified by changing the physicochemical properties of sulfated zirconia nanoparticles.