Kang Hongxing, He Dong, Yan Xingxu, Weed Melanie, Chai Jingtong, Turchiano Christopher, Pan Xiaoqing, Xiao Xiangheng, Gu Jing
Department of Chemistry and Biochemistry, San Diego State University, 5500 Campanile Drive, San Diego, California 92182, United States.
Department of Physics, Wuhan University, Wuhan, Hubei 430072, China.
Nano Lett. 2025 Jul 2;25(26):10626-10633. doi: 10.1021/acs.nanolett.5c02377. Epub 2025 Jun 21.
Transforming and repurposing plastic waste into valuable commodity chemical products is a sustainable strategy, which is beneficial for not only managing plastic waste but also fostering a circular plastic economy. Herein, we reported an electrocatalytic polyethylene terephthalate (PET) plastic waste upcycling to organonitrogen chemicals strategy over a MnO (MnO/CFP) catalyst. The MnO/CFP catalyst is capable of mildly oxidizing PET plastic-waste-derived ethylene glycol (EG) to electrophilic carbon intermediates under near-neutral conditions, in which the in situ formed carbon intermediates were stabilized and further attacked by nitrogenous nucleophiles, leading to the successful formation of amides. As a result, formamide (FE and yield up to 10.86% and 0.030 mmol cm h, respectively) was produced as the primary C-N coupling product with EG and ammonia (NH) as C and N sources, respectively. Furthermore, amides were synthesized with real-world PET plastic waste as the C source, indicating the potential practical application of this proof-of-concept work.
将塑料废物转化并重新利用为有价值的商品化学产品是一种可持续战略,这不仅有利于管理塑料废物,还能促进循环塑料经济。在此,我们报道了一种在MnO(MnO/CFP)催化剂上通过电催化将聚对苯二甲酸乙二酯(PET)塑料废物升级转化为有机氮化学品的策略。MnO/CFP催化剂能够在近中性条件下将PET塑料废物衍生的乙二醇(EG)温和氧化为亲电碳中间体,其中原位形成的碳中间体被稳定化,并进一步受到含氮亲核试剂的攻击,从而成功形成酰胺。结果,分别以EG和氨(NH₃)作为C和N源,生成了甲酰胺(FE和产率分别高达10.86%和0.030 mmol cm⁻² h⁻¹)作为主要的C-N偶联产物。此外,以实际的PET塑料废物作为C源合成了酰胺,表明了这项概念验证工作的潜在实际应用价值。