Fragmentation and depolymerization of microplastics in the earthworm gut: A potential for microplastic bioremediation?

The accumulation of microplastics poses potential risks to soil health. Here, we did a preliminary exploration on the potential of Lumbricus terrestris (Oligochaeta) to reduce low-density polyethylene (LDPE), polylactic acid (PLA), and polybutylene adipate terephthalate (PBAT) microplastic (20-648 µm) contamination in soils. The ingestion of microplastics-contaminated soil (1% of microplastics, dw/dw) in a mesocosm system and the ingestion of pure microplastics in the Petri Dish by earthworms were studied. Results show that earthworms survived in the microplastics-contaminated soil (0% mortality in 35 days) but barely when exposed solely to microplastics (30-80% mortality in 4 days). Size-dependent ingestion of microplastics was not observed. The fragmentation of LDPE microplastics in the gizzard facilitated by soil was confirmed by the significantly increased ratio of small-sized (20-113 µm) microplastics from the bulk soil to the gut (from 8.4% to 18.8%). PLA and PBAT microplastics were fragmented by gizzard without the facilitation of soil, the ratios of small-sized (20-113 µm) PLA and PBAT microplastics in the gut were 55.5% and 108.2% higher than in respective pristine distributions. Substantial depolymerization of PLA (weight-average molar mass reduced by 17.7% with shift in molecular weight distribution) and suspected depolymerization of PBAT were observed in the worm gut, while no change in the molar mass was observed for PLA and PBAT microplastics buried in the soil for 49 days. Our results suggest that ingested microplastics could undergo fragmentation and depolymerization (for certain polymers) in the earthworm gut. Further research is needed to reveal the mechanisms of polymer depolymerization in the earthworm gut and to evaluate the feasibility of microplastic bioremediation with earthworms.

Effect of Mineral Fillers on the Mechanical Properties of Commercially Available Biodegradable Polymers.

In the successful transition towards a circular materials economy, the implementation of biobased and biodegradable plastics is a major prerequisite. To prevent the accumulation of plastic material in the open environment, plastic products should be both recyclable and biodegradable. Research and development actions in the past few decades have led to the commercial availability of a number of polymers that fulfil both end-of-life routes. However, these biobased and biodegradable polymers typically have mechanical properties that are not on par with the non-biodegradable plastic products they intend to replace. This can be improved using particulate mineral fillers such as talc, calcium carbonate, kaolin, and mica. This study shows that composites thereof with polybutylene succinate (PBS), polyhydroxybutyrate-hexanoate (PHBH), polybutylene succinate adipate (PBSA), and polybutylene adipate terephthalate (PBAT) as matrix polymers result in plastic materials with mechanical properties ranging from tough elastic towards strong and rigid. It is demonstrated that the balance between the Young's modulus and the impact resistance for this set of polymer composites is subtle, but a select number of investigated compositions yield a combination of industrially relevant mechanical characteristics. Finally, it is shown that the inclusion of mineral fillers into biodegradable polymers does not negate the microbial disintegration of these polymers, although the nature of the filler does affect the biodegradation rate of the matrix polymer.