Investigation of Different Types of Biochar on the Thermal Stability and Fire Retardance of Ethylene-Vinyl Acetate Copolymers

In this work, three biochars, deriving from soft wood, oil seed rape, and rice husk and differing as far as the ash content is considered (2.3, 23.4, and 47.8 wt.%, respectively), were compounded in an ethylene vinyl acetate copolymer (vinyl acetate content: 19 wt.%), using a co-rotating twin-screw extruder; three loadings for each biochar were selected, namely 15, 20, and 40 wt.%. The thermal and mechanical properties were thoroughly investigated, as well as the flame retardance of the resulting compounds. In particular, biochar, irrespective of the type, slowed down the crystallization of the copolymer: this effect increased with increasing the filler loading. Besides, despite a very limited effect in flammability tests, the incorporation of biochar at increasing loadings turned out to enhance the forced-combustion behavior of the compounds, as revealed by the remarkable decrease of peak of heat release rate and of total heat release, notwithstanding a significant increase of the residues at the end of the tests. Finally, increasing the biochar loadings promoted an increase of the stiffness of the resulting compounds, as well as a decrease of their ductility with respect to unfilled ethylene vinyl acetate (EVA), without impacting too much on the overall mechanical behavior of the copolymer. The obtained results seem to indicate that biochar may represent a possible low environmental impact alternative to the already used flame retardants for EVA, providing a good compromise between enhanced fire resistance and acceptable mechanical properties.

The Flame Retardancy of Polyethylene Composites: From Fundamental Concepts to Nanocomposites

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.

Reactive and Additive Modifications of Styrenic Polymers with Phosphorus-Containing Compounds and Their Effects on Fire Retardance

Polystyrene, despite its high flammability, is widely used as a thermal insulation material for buildings, for food packaging, in electrical and automotive industries, etc. A number of modification routes have been explored to improve the fire retardance and boost the thermal stability of commercially important styrene-based polymeric products. The earlier strategies mostly involved the use of halogenated fire retardants. Nowadays, these compounds are considered to be persistent pollutants that are hazardous to public and environmental health. Many well-known halogen-based fire retardants, regardless of their chemical structures and modes of action, have been withdrawn from built environments in the European Union, USA, and Canada. This had triggered a growing research interest in, and an industrial demand for, halogen-free alternatives, which not only will reduce the flammability but also address toxicity and bioaccumulation issues. Among the possible options, phosphorus-containing compounds have received greater attention due to their excellent fire-retarding efficiencies and environmentally friendly attributes. Numerous reports were also published on reactive and additive modifications of polystyrene in different forms, particularly in the last decade; hence, the current article aims to provide a critical review of these publications. The authors mainly intend to focus on the chemistries of phosphorous compounds, with the P atom being in different chemical environments, used either as reactive, or additive, fire retardants in styrene-based materials. The chemical pathways and possible mechanisms behind the fire retardance are discussed in this review.

Evaluation of Asphalt with Different Combinations of Fire Retardants

When a fire takes place in a tunnel, the surface of the asphalt pavement will burn and release a large amount of smoke, which is toxic to human health. Thus, in order to prevent the combustion of the asphalt pavement under fire, it is necessary to propose some methods to retard its physical and chemical reaction under the high temperature. In this study, ten different combinations of fire retardants and a control case where no fire retardant was applied were prepared for evaluation. The thermogravimetric (TG)–mass spectrometry (MS) tests were used to evaluate their effect on the fire retardance from mass and energy perspectives and the Fire Dynamics Simulator (FDS) software was used to evaluate the fire retardance from temperature and smoke distribution perspectives. In experimental analysis, the TG (thermogravimetric) and DTG (differential thermogravimetric) curves were used to analyze the mass loss rate and residual mass of the asphalt and the activation energy was calculated and analyzed as well. In addition, decay rate of mass loss rate and increasing rate of activation energy were proposed to evaluate the ease of combustion of the asphalt with and without fire retardants. The results show that in laboratory experiments, the fire retardant combination which includes 48% aluminum hydroxide, 32% magnesium hydroxide, 5% expanded graphite, and 15% encapsulated red phosphorous would lead to an improved effect of fire retardance. In numerical modeling, the temperature and smoke height distribution over time were adopted to evaluate the fire retardance effect. The temperature distribution was found to be symmetrical on both sides of the combustion point and the same combination as proposed in experimental analysis was found to have the best effect on fire retardance due to the largest decrease in temperature. Additionally, because of the highest smoke height distribution, an improved effect on smoke suppression was also found when this combination was applied.

Cyclodextrins and Cyclodextrin Derivatives as Green Char Promoters in Flame Retardants Formulations for Polymeric Materials. A Review

Polymers are intrinsically flammable materials; hence, fire retardance (FR) is required in their most common applications (i.e., electronic and construction, to mention some). Recently, it has been reported that cyclodextrin (CD) and cyclodextrin derivatives are beginning to be introduced into Intumescent Fire Retardant (IFR) formulations in place of pentaerythritol, which is used in IFRs that are currently on the market. Since IFRs are of less environmental concern than their hazardous halogen containing counterparts, the use of natural origin compounds in IFRs provides a way to comply with green chemistry issues. BCD and BCD derivatives presence in IFR mixtures promotes a higher yield of blowing gases and char when polymeric materials undergo combustion. Both processes play important roles in intumescence. The key rule to obtain in insulating compact char is the good dispersion of the nanoparticles in the matrix, which can be achieved by functionalizing nanoparticles with BCD derivatives. Moreover, CD derivatives are attractive because of their nanosized structure and their ability to form inclusion complexes with many compounds used as FR components, reducing their release to the environment during their shelf life of FR items. Often, fire retardance performed by BCD and BCD derivatives accompanies other relevant properties, such as improved mechanical resistance, washability resistance, self healing ability, thermal conductivity, etc. The application of CD fire retardant additives in many polymers, such as poly(lactic acid), poly(propylene), poly(vinyl acetate), poly(methyl methacrylate), linear low density poly(ethylene), polyamides, and polyesters are comprehensively reviewed here.