Coagulation studies on photodegraded and photocatalytically degraded polystyrene microplastics using polyaluminium chloride

Abstract

Microplastics are ubiquitous persistent emerging contaminants, and its presence has been detected even in the most pristine and fragile ecosystems. Advanced oxidation processes are one of the novel degradation technologies used for the elimination of microplastics from the environment. In this study, the effect of ultraviolet C (UV-C, 253.7 nm) and ultraviolet A (UV-A, 365 nm) irradiations on polystyrene (PS) microplastic properties in the presence and absence of titanium dioxide were studied along with their coagulation performances using polyaluminium chloride (PAC). The effects of solar irradiation on the chemical properties of microplastics in aqueous and dry conditions were also investigated. PS microplastics (1.5 g) in three size ranges, 300–150 μm, 150–75 μm, and <75 μm were used during this experiment. After 45 days of irradiation, samples showed discolouration, brittleness, and loss of hydrophobicity. Images obtained from scanning electron microscope revealed smoothening and melting of PS surfaces upon UV exposure. Attenuated total reflectance- Fourier transform infrared spectroscopy and X-ray photon spectroscopy of photoaged samples revealed chemical alterations, bond cleavage and formation of oxygenated functional groups on microplastic surfaces. PAC coagulation of samples before and after UV irradiation showed drastic differences in removal efficiencies, with UV-C irradiated microplastics exhibiting maximum efficiency. Large sized and photocatalytically degraded microplastics showed better removal efficiencies than small sized particles. The 300–150 μm sized PS microplastic, degraded photo catalytically under UV-C irradiation showed approximately 99 % removal efficiency, while PS < 75 μm photodegraded under UV-A irradiation showed only 74.2 % removal efficiency.