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Breaking barriers in polymer tech: PBS vitrimers for greener futures

(a) DSC cooling scans; (b) The second DSC heating scans; (c) TGA curves; (d) DTG curves; (e) Storage modulus plots; (f) Digital photos showing heat resistance by observing deformation of the samples after maintaining at 150 °C for 30 min.

GA, UNITED STATES, December 27, 2024 /EINPresswire.com/ -- Recent advancements in polymer science have led to significant improvements in poly(butylene succinate) (PBS), a biodegradable polyester. By incorporating vitrimeric networks based on dynamic imine bonds, researchers have successfully enhanced PBS's melt viscosity and strength. This development addresses the material's previous limitations while preserving its environmentally friendly characteristics, making it a promising candidate for wider applications in sustainable materials across various industries.

Poly(butylene succinate) (PBS) has emerged as a viable alternative to conventional plastics due to its biodegradability and similar properties to polypropylene. Under composting conditions, PBS can break down into water, carbon dioxide, and biomass. However, its linear structure has limited its use in key manufacturing processes, such as foaming and film blowing, due to challenges with melt viscosity and mechanical strength. Overcoming these limitations has been a key focus for researchers seeking to expand PBS's potential in sustainable applications.

In a significant development, scientists from Southwest University, in collaboration with South China University of Technology, have enhanced PBS’s properties by introducing dynamic imine bonds. Their research (DOI: 10.1007/s10118-024-3132-6), published in the Chinese Journal of Polymer Science on May 17, 2024, details the creation of PBS vitrimers (PBSVs) that offer improved thermal, mechanical, and melt characteristics, positioning them as a more versatile material for eco-friendly applications.

By incorporating dynamic imine bonds into PBS, the research team developed vitrimeric networks that address the material’s melt viscosity and strength limitations. Adjusting the crosslinking degrees, the team synthesized PBSVs that exhibited notable improvements in performance. These vitrimers showed excellent thermal reprocessability, with more than 90% recovery of mechanical properties after three processing cycles. Additionally, higher crosslinking degrees led to faster crystallization rates, further enhancing material performance. Unlike traditional crosslinked polymers, these PBSVs maintain high viscosity and strength during processing, offering a more durable and sustainable alternative to conventional plastics.

Jian-Bing Zeng, the principal investigator of the study, emphasized the significance of their findings: “This research is an important step in advancing polymer science. We've successfully engineered PBSVs that maintain the sustainable, biodegradable properties of PBS while improving performance. These advances are crucial for broadening the use of biodegradable materials and could provide significant environmental benefits by offering more effective material options for applications traditionally dominated by non-degradable plastics.”

The development of these enhanced PBSVs holds considerable promise for industries focused on sustainability. With their improved melt properties and reprocessable nature, PBSVs could transform the production of eco-friendly packaging, foam materials, and disposable products. These materials offer a sustainable alternative to conventional plastics, helping to reduce environmental pollution. The widespread adoption of PBSVs could significantly decrease the ecological footprint of the plastics industry and support the transition to a circular economy, where materials are recycled and reused efficiently.

DOI
10.1007/s10118-024-3132-6

Original Source URL
https://doi.org/10.1007/s10118-024-3132-6

Funding information
This work was financially supported by the National Natural Science Foundation of China (No. 51973176), the Chongqing Talent Plan for Young Top-Notch Talents (No. CQYC2021059217) and the Fundamental Research Funds for the Central Universities (No. SWUXDJH202314).

Lucy Wang
BioDesign Research
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