Stability Assessment of a Polymeric Brominated Flame Retardant in Polystyrene Foams under Application-Relevant Conditions.

The flame retardant (FR) BLUEDGE polymeric flame retardant (PFR) has been in use since 2011 and was developed as a replacement FR for hexabromocyclododecane in polystyrene (PS)-based insulation foams. To better understand the degradation behavior of the PFR used within PS foams, we examined the degradation of PFR under application-relevant conditions. Thermo-oxidative and photolytic pathways represent the most relevant degradation pathways. Separately, both the thermal and oxidative degradations of PFR at ambient conditions were shown to be negligible based on kinetic models of thermogravimetric analysis data obtained at elevated temperatures; the models predict that it would take 100 years to degrade 1% of PFR at 50 °C and 1000 years at 20 °C. Photodegradation was shown to degrade PFR after accelerated ultraviolet (UV) aging/exposure. UV radiation did not significantly penetrate the foam insulation (<2000 µm); the degradation process took place primarily at the surface. The molecular weight of the polymer changed with degradation, but there was minimal loss of bromine from the foam with degradation. The data from the liquid chromatography-mass spectrometry analysis focused primarily on several small-molecule polar products formed, which included two brominated species. These species were predicted using computer-based modeling to be biodegradable, to not be persistent in the environment, and to exhibit a low toxicity to aquatic organisms.

Assessing the environmental impact due to photolytic degradation of ethane-bis(pentabromophenyl) in plastics.

Photolytic degradation of brominated flame retardants is one of the potential decomposition pathways in the environment, and for some flame retardants such as ethane-bis(pentabromophenyl) (EBP), also called decabromodiphenyl ethane, there are concerns that degradation products may be harmful. In this paper, we present photolytic studies of EBP in high-impact polystyrene (HIPS) and polypropylene impact copolymer (PP) using accelerated weatherometry. The half-life of photolytic debromination of EBP in HIPS was estimated to be more than 200 years, which can be contrasted with half-lives of minutes for photolysis conducted on dilute EBP solutions. Perhaps more importantly, there was no subsequent debromination to the octabrominated congeners or lower. No evidence of debromination was seen in PP, which confirms the importance of matrix effects. We also saw no evidence of accelerated resin photooxidation caused by EBP. These studies demonstrate that EBP is much more photolytically stable in resins than structurally-similar decabromodiphenyl ether, and a read-across comparison between the two flame retardant molecules for this degradation pathway is misleading.