Secondary microplastics formation and colonized microorganisms on the surface of conventional and degradable plastic granules during long-term UV aging in various environmental media.

Recently, biodegradable plastics (BPs) as an alternative of conventional plastics have been widely advocated and applied. However, there is still a large research gap between the formation of secondary microplastics (MPs) and colonized microorganisms on their surface under long-term aging in different environments. In this study, the generation of secondary MPs and the formation of surface biofilms on the micro-sized (3-5 mm) biodegradable plastic poly (butyleneadipate-co-terephthalate) (BP-PBAT) and conventional plastic polyvinyl chloride (CP-PVC) under long-term UV aging was investigated. The results showed that hundreds and even thousands of MPs (185.53 ± 85.73 items/g - 1473.27 ± 143.67 items/g) were generated by BP-PBAT and CP-PVC after aged for 90 days, and the abundance of MPs produced by BP-PBAT was significantly higher than that of CP-PVC. Moreover, the α diversities and detected OTU number of biofilm communities formed on MPs increased with MPs-aging. The genes related to the formation of biofilms was significantly expressed on aged MPs and the genes related to human pathogens and diseases were also detected in enriching on MPs surface. Overall, BPs may lead to greater ecological risks as it releases thousands of secondary MPs after being aged, and their environmental behavior needs to be further explored.

Aging of biodegradable blended plastic generates microplastics and attached bacterial communities in air and aqueous environments.

The use of biodegradable plastics (BPs) has been widely promoted in recent years, but before their complete degradation, the phase of microplastics (MPs) is inevitable. However, little information concerning the production of MPs from blended polymers is available. This study aimed to explore the characteristics of MPs produced from blended plastics and the development of biofilms on plastic surfaces under long-term aging. Here, three blended materials (i.e., PBAT (53%)+PLA (10%)+Starch (20%), PBAT (80%)+Starch (20%), HDPE (60%)+CaCO3 (40%)) were aged for 90 days in air, deionized (DI) water and seawater. The results showed massive production of MPs (9653 ± 3920-20,348 ± 5857 items/g) from blended plastics accompanied by a large quantity of flocculent substances during 90 days aging period. Furthermore, the richness of bacteria communities on hydrophobic plastics (i.e., PBAT (53%)+PLA (10%)+Starch (20%), PBAT (80%)+Starch (20%)) was higher than hydrophilic plastics (i.e., HDPE (60%)+CaCO3 (40%)), and bacterial communities attached to blended plastics exhibited significantly variation with aging times. Overall, promoting the marketable application of blended plastics is risky if their environmental behavior is not effectively addressed.