Strawberries are valuable because of their nutritional value, but they are also highly perishable fruits. Fungal decay is the overriding factor that alters the overall quality of fresh strawberries. Because no hygienic treatments to reduce the initial microbial load are feasible, molds develop during postharvest when using conventional packaging. In this study, an antifungal packaging system for strawberries was developed to improve safety and quality. Trans-2-hexenal (HXAL), a natural compound in strawberries, was incorporated into the modified atmosphere packaging (MAP) systems. Zero, 100, and 250 µL of HXAL were included in cellulosic pads and were covered with a polyamide coating to control its release. The pads were placed on the bottom of plastic trays; an amount of250 g of strawberries was added, flow packed in micro-perforated PP bags, and stored at 4 °C for 14 days. Fungal infection was monitored during the storage period, and the optical and textural properties of the strawberries were measured at days 0 and 14. Analysis of the package headspace was conducted to check for the HXAL concentration. HXAL was partially retained in the fruits and was converted into hexyl acetate and 2-hexen-1-ol acetate, but this was only measurably present in the headspace of the active systems. Mold growth was fully inhibited in active packaging although the strawberries were softer and darker than those in the control packages. The active package was not as efficient if the fruits were stored under thermal-abuse conditions (15 and 22 °C).

Microplastics (MPs) are recognised as emerging vectors for hydrophobic organic contaminants in aquatic environments due to their relatively large surface area and the diversity of their polymer chemistries compositions. This study investigates the sorption behaviour of two priority polycyclic aromatic hydrocarbons (PAHs), pyrene (PYR) and fluoranthene (FLU), onto six common MPs: poly(m-xylene adipamide) (PA-MXD6), high- and low-density polyethylene (HDPE, LDPE), polypropylene (PP), polyethylene terephthalate (PET), and polylactic acid (PLA). Sorption isotherms and kinetics were evaluated under simulated freshwater conditions at environmentally relevant concentrations (1–50 µg·L⁻¹). Despite the low MP concentration used (0.2 g·L⁻¹), over 80% of the initial PAH content was removed by polyolefins, and more than 50% by all other MPs. Sorption capacity was strongly dependent on particle surface area. Langmuir, Henry, and Freundlich isotherms models were fitted, with linear behaviour prevailing at low concentrations. Analysis using the Dubini–-Radushkevich model confirmed that sorption involves chemisorption contributions, mainly through π–π interactions and hydrophobic interactions (polyolefins). Mechanistically, molecular diffusion within the MP matrix was not governing the sorption process, as diffusion coefficients varied with particle size instead of polymer chemistry. Instead, sorption appears to be governed by PAH diffusion through the hydrodynamic boundary layer and subsequent retention on the MP surface. Empirically, kinetic data fitted the pseudo-second-order model, further supporting that the sorption process involves chemisorption. These findings highlight the role of MPs as vectors for PAHs in freshwater systems and their potential application in contaminant removal. Expressing sorption per unit surface area is recommended for accurate assessment. This work contributes to understanding the environmental behaviour of MPs and their implications for pollutant transport and toxicity.

This study presents a theoretical framework for modeling sorption and release kinetics of substances in polymeric materials with planar, cylindrical, and spherical geometries. Fick’s second law was expressed in dimensionless variables and solved numerically using a finite-difference approach to generate universal profiles for mass transfer. These profiles were fitted with double-exponential equations, yielding explicit expressions that allow for straightforward estimation of diffusion coefficients from experimental data. The method was validated using literature data for films, fibers, and microspheres, showing excellent agreement with reported values. Unlike classical analytical solutions, which are limited to planar systems under ideal conditions, the proposed approach is applicable to diverse geometries commonly employed in packaging, biomedical devices, controlled-release formulations, and environmental technologies.