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<p>Conventional alcoholysis processes for polycarbonate (PC) recycling require excess methanol input, high reaction temperatures and complicated downstream product separation steps, severely limiting environmental and economic sustainability. Here we report a facile, self-driven tandem alcoholysis process to address these challenges. Methanol-based PC alcoholysis reaction is coupled to a downstream glycerol transesterification step to rapidly convert the dimethyl carbonate intermediate into methanol, thus forming a closed-loop methanol flow to boost the overall reactions. Additionally, the reactions are catalyzed by eggshell-derived multimetallic CaO, which provides abundant acid–base sites for synergistically deprotonating alcohols and activating ester bonds to facilitate a selective conversion. This integrated design not only enables 98.8% less methanol usage and significantly lower reaction temperature than the PC-alone alcoholysis process&#xa0;(80 °C versus &gt;130 °C), but also generates bisphenol A (96% yield) and 5-hydroxymethyl-1,3-dioxolan-2-one (90% yield) as higher-value products. The process is adaptable to treating mixed-plastic feeds with robust performance. The pilot-scale trials (&gt;5 kg) using real mixed plastic waste demonstrate superior upcycling performance and distinctly improved environmental and economic benefits over the existing industrial synthesis routes. Overall, this scalable, self-driven tandem alcoholysis process offers a sustainable, industrially-viable platform for upcycling PC-containing waste plastics.</p>

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Self-driven tandem alcoholysis for full upcycling of waste polycarbonate plastics

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年4月30日

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  • Yuan Kong,
  • Yu-Ze Cheng,
  • Si-Xian Wang,
  • Wu-Jun Liu,
  • Zhi-Yan Guo,
  • Han-Qing Yu,
  • Wen-Wei Li

摘要

Conventional alcoholysis processes for polycarbonate (PC) recycling require excess methanol input, high reaction temperatures and complicated downstream product separation steps, severely limiting environmental and economic sustainability. Here we report a facile, self-driven tandem alcoholysis process to address these challenges. Methanol-based PC alcoholysis reaction is coupled to a downstream glycerol transesterification step to rapidly convert the dimethyl carbonate intermediate into methanol, thus forming a closed-loop methanol flow to boost the overall reactions. Additionally, the reactions are catalyzed by eggshell-derived multimetallic CaO, which provides abundant acid–base sites for synergistically deprotonating alcohols and activating ester bonds to facilitate a selective conversion. This integrated design not only enables 98.8% less methanol usage and significantly lower reaction temperature than the PC-alone alcoholysis process (80 °C versus >130 °C), but also generates bisphenol A (96% yield) and 5-hydroxymethyl-1,3-dioxolan-2-one (90% yield) as higher-value products. The process is adaptable to treating mixed-plastic feeds with robust performance. The pilot-scale trials (>5 kg) using real mixed plastic waste demonstrate superior upcycling performance and distinctly improved environmental and economic benefits over the existing industrial synthesis routes. Overall, this scalable, self-driven tandem alcoholysis process offers a sustainable, industrially-viable platform for upcycling PC-containing waste plastics.