Plastic production has outgrown most other manmade materials, with more than 90% being petroleum-based and nonbiodegradable. Packaging, primarily food packaging, consumes the most plastic and is the largest contributor to municipal solid waste. In addition, its dependence on crude oil feedstock makes the plastic industry unsustainable and renders plastic markets vulnerable to oil price volatility. Therefore, the development of bioalternatives to conventional plastics is now a priority of the food packaging industry. Bioplastics are polymers that are either biobased (fully or partially), or biodegradable, or both. This review aims to provide an insightful overview of the most recent research and development successes in bioplastic materials, focusing on food packaging applications. Bioplastics are compared to their conventional counterparts with respect to their mechanical, thermal, barrier, and processability properties. The gaps between bio-and conventional plastics in food packaging are elucidated. Potential avenues for improving bioplastic properties to broaden their food packaging applications are critically examined. Furthermore, two of the most controversial topics on bioplastic alternatives, sustainability assessment and their impact on the plastic waste management system, are discussed.

Poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) is a promising bio-based and biodegradable thermoplastic with restricted industrial applications due to its brittleness and poor processability. Natural rubber (NR) has been used as a toughening agent, but further physical improvements are desired. In this study, rubber toughening efficiency was significantly improved through the synergistic use of a trifunctional acrylic coagent and an organic peroxide during reactive extrusion of PHBV and NR. The rheological, crystallization, thermal, morphological, and mechanical properties of PHBV/NR blends with 15% rubber loading were characterized. The peroxide and coagent synergistically crosslinked the rubber phase and grafted PHBV onto rubber backbones, leading to enhanced rubber modulus and cohesive strength as well as improved PHBV–rubber compatibility and blend homogeneity. Simultaneously, the peroxide–coagent treatment decreased PHBV crystallinity and crystal size and depressed peroxy-radical-caused PHBV degradation. The new PHBV/NR blends had a broader processing window, 75% better toughness (based on the notched impact strength data), and 100% better ductility (based on the tensile elongation data) than pristine PHBV. This new rubber-toughened PHBV material has balanced mechanical performance comparable to that of conventional thermoplastics and is suitable for a wide range of plastic applications.

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Polyamide (PA)–graphene oxide (GO) composite membranes were fabricated to enhance pervaporation desalination for hypersaline solutions. Thin- and stripe-structured PA layers were formed on a base GO membrane via interfacial polymerization, which enhanced the hydrophilicity of the membrane surface and provided more active sites for enrichment and permeation of water molecules. The water flux through prepared membranes could reach up to 26.7 kg m–2 h–1 with 99.99% salt rejection for 3.5 wt % NaCl aqueous solution under 70 °C. When the feed salt concentration was increased to 10 wt %, the water flux could keep a high level (ca. 24.0 kg m–2 h–1) with an ideal ion rejection (99.99%). Moreover, satisfactory performance could be preserved in a long-term test for the prepared PA–GO composite membrane. All of the results demonstrate that PA–GO composite membranes prepared in this study have great application prospects in practical pervaporation desalination of hypersaline seawater or aqueous solutions.

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As a typical catalytic reaction model, CO catalytic oxidation has many practical applications in gas purification. TiO2 supported Pt sub-nanoclusters have been prepared by introducing variable valence Co ions into a one step flame spray pyrolysis process. Co2+ was oxidized to Co3+ in the high-temperature flame, and the released electrons were transferred to the surface of Pt and suppressed the aggregation of Pt nanoclusters supported on TiO2. As a result, the average size of Pt nanoclusters reduced from 2.47 nm to 0.72 nm with only 1% Co2+ ion doping. Moreover, due to the presence of Co, surface oxygen species were also affected, and these changes also led to a significant increase in the catalytic activity of CO oxidation. The temperature at 100% conversion was decreased from 120 °C to 70 °C, and the TOF increased by an order of magnitude. In addition, in situ DRIFTS was also used to investigate the cause of the significant increase in activity, and it was shown that adsorbed CO species on Pt could be desorbed more easily because of the electron transfer between Pt and Co species.