As the global plastic pollution problem intensifies and the environmental hazards of traditional petroleum-based plastics become increasingly significant, the development of sustainable alternative materials has become an urgent need. This paper systematically reviews the research progress, application status and future trends of new generation bioplastics in the field of food packaging. Bioplastics are categorized into three main groups according to their sources and degradability: biobased biodegradable materials (e.g., polylactic acid PLA, polyhydroxy fatty acid ester PHA, chitosan, and cellulose-based materials); biobased non-biodegradable materials (e.g., Bio-PE, Bio-PET); and non-biobased biodegradable materials (e.g., PBAT, PCL, PBS). Different processing technologies, such as thermoforming, injection molding, extrusion molding and coating technologies, can optimize the mechanical properties, barrier properties and freshness retention of bioplastics and promote their application in scenarios such as food containers, films and smart packaging. Although bioplastics still face challenges in terms of cost, degradation conditions and industrial support, promising future directions are found in the development of the large-scale utilization of non-food raw materials (e.g., agricultural waste, algae), nano-composite technology to enhance the performance, and the development of intelligent packaging functions. Through technological innovation and industry chain integration, bioplastics are expected to transform from an environmentally friendly alternative to a mainstream packaging material, helping to realize the goal of global carbon neutrality.

Flexible wearable sensors show great potential for applications in wearable devices, remote health monitoring, artificial intelligence, soft robotics, and artificial skin due to their stretchability, bendability, thinness and portability, and excellent electrical properties. Hydrogels have tunable mechanical properties, excellent biocompatibility, and flexibility, making them attractive candidates for wearable flexible sensors. Among them, tremendous efforts have focused on the advancement of chitosan-based hydrogels (CS-Gels) to realize multifunctional wearable sensing by modifying hydrogel networks with additives/nanofillers/functional groups. Recently, remarkable progress has been made in flexible wearable sensors. Herein, this review summarizes recent advances in CS-Gels wearable sensors for applications such as human motion monitoring, health monitoring, human-machine interface and soft robotics. Representative synthesis methods and strategies for CS-Gels are briefly described, the problems and deficiencies of CS-Gels for wearable sensors are discussed. Finally, the possible opportunities and challenges for the future development of CS-Gels flexible wearable devices are proposed.

Carboxymethyl cellulose (CMC)/polyvinyl alcohol (PVA) composite nanofiber membranes were prepared by electrostatic spinning, using CMC and PVA as raw materials and glutaraldehyde as a cross-linking agent. The structure, morphology, thermal stability, and filtration performance of CMC/PVA nanofiber membranes were characterized by advanced instrumental analysis methods such as scanning electron microscopy, Fourier transform infrared spectroscopy, thermogravimetric analysis, ultraviolet analysis, and energy spectrum analysis. The results show that the average fiber diameter decreases from 381 nm to 183 nm when the spinning voltage is 23 KV and the jet speed is 2 µL/min. The obtained fiber has the smallest particle size and the most uniform distribution. Infrared spectroscopy analysis confirms that the adsorption behavior of nanofiber membranes on Cu²⁺ and Cr⁶⁺ is chemical adsorption. The retention rates of CMC/PVA nanofiber membranes for Cu²⁺ and Cr⁶⁺ reached 97.2% and 98.8%, respectively. The adsorption capacities of Cu²⁺ and Cr⁶⁺ were 26.34 and 28.93 mg·g⁻¹, respectively. The adsorption of heavy metal ions by nanofiber membranes can be explained by the pseudo-second-order kinetic mechanism of the chemisorption process and the Langmuir isotherm model.

In pursuit of sustainable solutions for water pollution mitigation, we have successfully employed electrospinning technology to fabricate a multilayered sodium alginate (SA)/polyethyleneimine (PEI)/polyvinyl alcohol (PVA) nanocomposite fiber membrane, with a focus on enhancing its adsorption capacity for Cu²⁺ ions in wastewater. Our research underscores the potential of this novel membrane, characterized by its small diameter, high uniformity, and expansive surface area, in effectively filtering heavy metal ions. By optimizing critical electrospinning parameters such as a voltage of 19.5 KV, a collector distance of 8 cm, a specific mass ratio of SA:PEI: PVA (1:2:6), and an injection rate of 8 μL/min, we achieved a nanofiber membrane with an average diameter of 112.5 nm, exhibiting exceptional morphological characteristics and high efficiency. Notably, the membrane exhibited an adsorption capacity of over 85% for Cu²⁺ during initial testing, maintaining over 80% efficiency throughout four consecutive filtration cycles. This work not only advances the field of nanocomposite membranes for water purification but also contributes significantly to the broader goal of achieving environmental sustainability by mitigating the impact of heavy metal contamination in water bodies.

In this study, multilayer composite nanofiber membranes of sodium alginate (SA) /polyethyleneimine (PEI)/polyvinyl alcohol (PVA) was fabricated via electrospinning technique to enhance the adsorption of Cu2+ from wastewater. The preparation and adsorption mechanisms of the SA/PEI/PVA nanofiber membranes were analyzed by utilizing analytical techniques such as SEM, FTIR, EDS, UV-vis, XRD, and TG. The obtained nanofiber membrane characterized by small diameter, high uniformity, and extensive surface area, demonstrate significant potential for heavy metal ion filtration. Optimal spinning parameters were identified, including a voltage of 19.5 KV, a distance of 8 cm, and specific mass ratios (SA: PEI: PVA, 1:2:6) and injection speeds (8 μL/min) and. The resulting nanofibers with an average diameter of 112.5 nm exhibited excellent morphology and high efficiency, retaining over 85% adsorption capacity for Cu2+ in initial tests and maintaining above 80% efficacy through four successive filtration cycles.