Accelerated fragmentation of two thermoplastics (polylactic acid and polypropylene) into microplastics after UV radiation and seawater immersion

Type Article
Date 2024-02
Language English
Author(s) Niu Zhiyue1, 2, Curto Marco3, Le Gall Maelenn4, Demeyer Elke5, Asselman Jana2, Janssen Colin R2, Dhakal Hom Nath3, Davies PeterORCID4, Catarino Ana Isabel1, Everaert Gert1
Affiliation(s) 1 : Flanders Marine Institute (VLIZ), InnovOcean Campus, Jacobsenstraat 1, 8400 Oostende, Belgium
2 : Blue Growth Research Lab, Ghent University, Bluebridge Building, Ostend Science Park 1, 8400 Ostend, Belgium
3 : Advanced Polymers and Composites (APC) Research Group, School of mechanical and Design Engineering, University of Portsmouth, Portsmouth PO1 3DJ, UK
4 : Marine Structures Laboratory, IFREMER, Centre de Bretagne, 29280, France
5 : Functional Thermoplastic Textiles, Centexbel, Industriepark Zwijnaarde 70, 9052 Gent, Belgium
Source Ecotoxicology And Environmental Safety (0147-6513) (Elsevier BV), 2024-02 , Vol. 271 , P. 115981 (10p.)
DOI 10.1016/j.ecoenv.2024.115981
Keyword(s) Fragmentation, Microplastics formation, Bio-based plastics, Polylactic acid, Ultraviolet radiation, Polypropylene
Abstract

To better understand the fate and assess the ingestible fraction of microplastics (by aquatic organisms), it is essential to quantify and characterize of their released from larger items under environmental realistic conditions. However, the current information on the fragmentation and size-based characteristics of released microplastics, for example from bio-based thermoplastics, is largely unknown. The goal of our work was to assess the fragmentation and release of microplastics, under ultraviolet (UV) radiation and in seawater, from polylactic acid (PLA) items, a bio-based polymer, and from polypropylene (PP) items, a petroleum-based polymer. To do so, we exposed pristine items of PLA and PP, immersed in filtered natural seawater, to accelerated UV radiation for 57 and 76 days, simulating 18 and 24 months of mean natural solar irradiance in Europe. Our results indicated that 76-day UV radiation induced the fragmentation of parent plastic items and the microplastics (50 - 5000 µm) formation from both PP and PLA items. The PP samples (48 ± 26 microplastics / cm2) released up to nine times more microplastics than PLA samples (5 ± 2 microplastics / cm2) after a 76-day UV exposure, implying that the PLA tested items had a lower fragmentation rate than PP. The particles’ length of released microplastics was parameterized using a power law exponent (α), to assess their size distribution. The obtained α values were 3.04 ± 0.11 and 2.54 ± 0.06 (-) for 76-day UV weathered PP and PLA, respectively, meaning that PLA microplastics had a larger sized microplastics fraction than PP particles. With respect to their two-dimensional shape, PLA microplastics also had lower width-to-length ratio (0.51 ± 0.17) and greater fiber-shaped fractions (16%) than PP microplastics (0.57 ± 0.17% and 11%, respectively). Overall, the bio-based PLA items under study were more resistant to fragmentation and release of microplastics than the petroleum-based PP tested items, and the parameterized characteristics of released microplastics were polymer-dependent. Our work indicates that even though bio-based plastics may have a slower release of fragmented particles under UV radiation compared to conventional polymer types, they still have the potential to act as a source of microplastics in the marine environment, with particles being available to biota within ingestible size fractions, if not removed before major fragmentation processes.

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How to cite 

Niu Zhiyue, Curto Marco, Le Gall Maelenn, Demeyer Elke, Asselman Jana, Janssen Colin R, Dhakal Hom Nath, Davies Peter, Catarino Ana Isabel, Everaert Gert (2024). Accelerated fragmentation of two thermoplastics (polylactic acid and polypropylene) into microplastics after UV radiation and seawater immersion. Ecotoxicology And Environmental Safety, 271, 115981 (10p.). Publisher's official version : https://doi.org/10.1016/j.ecoenv.2024.115981 , Open Access version : https://archimer.ifremer.fr/doc/00872/98402/