Every year, almost 1.15-2.41 million tons of plastic from terrestrial rivers undergo fragmentation under certain conditions and settle in the estuarine delta and shallow marine shelf areas, making this region a \"sink\" for land-based microplastics. Owing to its fast deposition rate, relatively soft sediment bed, and shallow water depth, the estuarine delta region is prone to liquefaction under high wind and wave conditions. This could potentially release deeply buried microplastic particles during the liquefaction process, posing further threats to marine ecology and human health. To investigate this phenomenon, laboratory experiments were conducted using a water tank to simulate wave-induced liquefaction of sediment beds. The results showed that under the influence of wave-induced liquefaction, 56.2 % of microplastic particles were released back into the sediment surface, with larger particles being released to a greater extent. Based on these experimental results, this study also analyzed and discussed the release rate and mechanisms of microplastic particles from sediment during wave-induced liquefaction, estimating that the maximum release rate of microplastic particles under the experimental conditions could reach 0.34 mm/min.

Global concern over microplastics (MPs) is increasing because of the potential threat these substances pose to ecosystem and human health. Disposable cups, frequently used as containers of beverages, are typically made of plastic or plastic-coated paper. The release of MPs from disposable cups during use may provide a direct exposure pathway for humans. In this study, the MP release capacities of 90 batches of commercial disposable cups, including polyethylene (PE)-coated paper cups, polypropylene (PP) cups, and polystyrene (PS) cups, were investigated under daily use conditions, and the properties of released MP particles are characterized with Raman spectroscopy, scanning electron microscopy (SEM), and atomic force microscopy (AFM). The MPs release into containing beverages is detected for each of the tested cups in this study. The released MPs particles are in irregular shapes and dominantly smaller than 20 μm. The quantities of released MPs are in the range of 675-5984, 781-4951, and 838-5215 particles/L for PE-coated paper cups, PP cups and PS cups, respectively, when containing pure water at 95 °C for 20 min. No significant difference in the quantity of MP released is observed among the three types of the cups in the experimental conditions. High temperature is found to promote the release of MPs from disposable cups. The MP release is notable when the cups are used for a second time, although at a slightly lower level than the first use. Acidic carbonated beverages obviously enhance MP release from PE-coated cups over that of ultrapure water.

Microplastic particles and fibers are increasingly being detected in our surface and ground waters as well as within a wide range of aquatic species. Their presence in the environment is largely due to in situ generation from physical and chemical weathering of larger plastics, and thus has left environmental community concerned in the post-banned era of microbead use in personal care products through the passage of Microbead-Free Waters Act in the United States. To improve understanding of secondary microplastic formation, accelerated weathering has been conducted on four materials (high-density polyethylene, high impact polystyrene, nylon 6, and polypropylene) under ultraviolet radiation (equivalent to 44 days in full sun) in simulated seawater. Physical and chemical characterization of the plastics were completed following ultraviolet exposure. This simulated weathering generated microfibers from high-density polyethylene and nylon 6, while high impact polystyrene and polypropylene did not physically degrade. The techniques used were applied to sediment samples containing plastic pellets collected from Cox Creek in Port Comfort, TX (near a large plastics manufacturer), which were purified for analysis and were found to contain microplastics composed of polypropylene and polyethylene. These findings can be used to determine degradation pathways and plastic source tracking, which can facilitate risk assessment and environmental management.