RESUMO
Limited information exists on the potential of aged microplastics to induce photodegradation of organic pollutants under sunlight irradiation. In this work, nicotine (NIC), a widespread emerging contaminant, was used as a model organic substrate to investigate this innovative degradation process. Polystyrene (PS) pellets were artificially aged and became rich in oxygenated moieties with their carbonyl index reaching 0.43 ± 0.04 after 4 d of aging. The degradation of NIC photosensitized by aged PS at different pH values was monitored for 6 h under simulated sunlight irradiation (650 W/m2). The maximum degradation rate was observed at pH = 11 (75 % NIC removal from a 10 mg L-1 solution containing 50 g L-1 aged PS pellets), suggesting that the unprotonated NIC is the most photoreactive form. Increasing the PS load from 50 to 200 g L-1 accelerated NIC degradation. The addition of 2.5 mg L-1 humic acids had a slight enhancement role (82 % NIC degradation), which confirms their effectiveness as photosensitizers. NIC photosensitization by aged PS was also studied in the presence of t-butanol (55 % NIC removal in solutions containing 100 mg L-1 t-butanol) and in anoxic conditions (NIC solution purged with N2; 95 % NIC removal), to gain insight into the respective roles of the potentially formed â¢OH and 1O2. The main photo-produced reactive species involved in NIC degradation likely were the triplet states of the PS beads (3PS*). Differently from most advanced oxidation processes, NIC's photodegradation by aged PS was not affected by increasing amount of chloride and we observed negligible differences between NIC degradation in ultra-pure water and seawater. The effectiveness of irradiated PS towards NIC photodegradation was also investigated in tap water and secondary wastewater. Overall, the possibility to decontaminate polluted water with waste-derived materials is interesting in the framework of circular economy.
