Pietro Bonechi , Irina Kandylioti , Alessandra Cincinelli , Ioana Alexandra Ionescu , Elefteria Psillakis
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引用次数: 0
Abstract
In this study, we argue that the Carbonyl Index (CI) values of weathered microplastics with carbon–carbon backbones can reliably predict their ability to enhance indirect photodegradation of organics under solar light, an effect that is independent of the type of polymer used. Polystyrene (PS), polypropylene (PP), and low-density polyethylene (LDPE) pellets were artificially weathered under UV-C, either in ambient air or submerged in water. Surface changes were characterized using ATR-FTIR spectroscopy, and the CI values were calculated. PS exhibited a much higher weathering rate than PP and LDPE, with air exposure being more effective than water for all plastic types. Nicotine (NIC) was used as the model organic compound. NIC photodegradation (10 mg L−1) was monitored in the presence of each weathered pellet type (50 g L−1) for 6 h under simulated sunlight at pH 11. The apparent pseudo-first-order rate constants, k, were 0.025 ± 0.015 h−1 (air-weathered LDPE), 0.036 ± 0.002 h−1 (water-weathered PP), 0.079 ± 0.029 h−1 (air-weathered PP), 0.216 ± 0.014 h−1 (water-weathered PS), and 0.346 ± 0.016 h−1 (air-weathered PS). A linear correlation (R2 = 0.956) was found between CI and k, indicating that photodegradation is primarily governed by the degree of aging rather than the polymer type. This relationship was further validated using naturally weathered PS and PP items collected from beaches, which aligned with the established CI–k correlation. These findings suggest that the CI is a practical indicator for predicting the environmental reactivity of weathered microplastics.
期刊介绍:
JPPA publishes the results of fundamental studies on all aspects of chemical phenomena induced by interactions between light and molecules/matter of all kinds.
All systems capable of being described at the molecular or integrated multimolecular level are appropriate for the journal. This includes all molecular chemical species as well as biomolecular, supramolecular, polymer and other macromolecular systems, as well as solid state photochemistry. In addition, the journal publishes studies of semiconductor and other photoactive organic and inorganic materials, photocatalysis (organic, inorganic, supramolecular and superconductor).
The scope includes condensed and gas phase photochemistry, as well as synchrotron radiation chemistry. A broad range of processes and techniques in photochemistry are covered such as light induced energy, electron and proton transfer; nonlinear photochemical behavior; mechanistic investigation of photochemical reactions and identification of the products of photochemical reactions; quantum yield determinations and measurements of rate constants for primary and secondary photochemical processes; steady-state and time-resolved emission, ultrafast spectroscopic methods, single molecule spectroscopy, time resolved X-ray diffraction, luminescence microscopy, and scattering spectroscopy applied to photochemistry. Papers in emerging and applied areas such as luminescent sensors, electroluminescence, solar energy conversion, atmospheric photochemistry, environmental remediation, and related photocatalytic chemistry are also welcome.