Polypropylene is one of the most widely produced plastics, but its mechanical properties decline during recycling because of irreversible polymer chain breakage, limiting reuse and slowing the development of a circular polyolefin economy. Here we present a dual-dynamic vitrimer approach that converts post-consumer recycled polypropylene into a high-performance and fully recyclable material through covalent adaptable networks. A scalable two-step reactive extrusion process, involving glycidyl methacrylate grafting followed by the addition of 2,2′-dithiodibenzoic acid, creates a network that combines transesterification with reversible disulfide exchange. Gel fraction and rheological measurements confirm the formation of a stable yet reprocessable structure. The vitrimer shows a 24% increase in yield strength, a 31% increase in Young’s modulus, a twofold increase in complex viscosity, and a 9 °C increase in crystallization temperature. These properties remain stable after five recycling cycles. Molecular simulations, fused granulate fabrication, and techno-economic analysis further demonstrate network stability, manufacturability, and industrial potential. This strategy offers a scalable route for upcycling polyolefin waste into durable and recyclable materials. A dual-dynamic vitrimer network enhances yield strength by 24%, increases Young’s modulus by 31%, doubles complex viscosity, and retains performance through five recycling cycles, according to a two-step reactive extrusion process for post-consumer recycled polypropylene.
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Bohra et al. (2026) studied this question.
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