Degradability and biofouling of oxo-biodegradable polyethylene in the planktonic and benthic zones of the Arabian Gulf.

Little is known about the degradability of oxo-biodegradable polyethylene (OXO-PE) and its surface fouling bacterial communities in the marine environment. The degradation of OXO-PE, PE and polyethylene terephthalate (PET) was compared at two depths (2 m and 6 m) in the Arabian Gulf. Scanning electron microcopy (SEM) revealed more fissure formation on OXO-PE and PE than on PET, indicating physical degradation. The formation of hydroxyl groups and carbonyl bonds, by Fourier-transform infrared spectroscopy (FTIR), suggests chemical degradation of OXO-PE. Plastisphere bacterial communities on OXO-PE and PE were different than on PET. Proteobacteria, Bacteriodetes and Planctomycetes were detected on all plastics, however, sequences of Alteromonas and Zoogloea were OXO-PE-specific suggesting a possible involvement of these bacterial genera in OXO-PE degradation. We conclude that OXO-PE shows increased signs of degradation with time owing to the combination of abiotic and biotic processes, and its degradation is higher in the benthic than in the planktonic zone.

Glassy states in asymmetric mixtures of soft and hard colloids.

By employing rheological experiments, mode coupling theory, and computer simulations based on realistic coarse-grained models, we investigate the effects of small, hard colloids on the glassy states formed by large, soft colloids. Multiarm star polymers mimic hard and soft colloids by appropriately varying the number and size of their arms. The addition of hard colloids leads, depending on their concentration, to either melting of the soft glass or the emergence of two distinct glassy states. We explain our findings by depletion of the colloids adjacent to the stars, which leads to an arrested phase separation when the repulsive glass line meets the demixing binodal. The parameter-free agreement between experiment, theory, and simulations suggests the generic nature of our results and opens the route for designing soft-hard colloidal composites with tunable rheology.