Self-doping of biological secretions for waste catalyst reuse

催化作用 重新使用 碳化 废物管理 吸附 环境科学 流出物 化学 碳纤维 化学工程 废物处理 持续性 再生(生物学) 材料科学 焚化 多相催化 炼油厂 金属 资源回收 废弃物 催化剂载体
作者
Min Li,Liya Fu,Yue Yuan,Yu Yin,Xiaoguang Jin,Zhouyang Li,Yi Zeng,Xiang Liu,Chunli Wan,Yu Sun,Min Xu,Panxin Wang,Hongbo Xi,Yudong Song,Qi Huang,Yuexi Zhou,Changyong Wu
出处
期刊:Nature Communications [Nature Portfolio]
卷期号:16 (1): 10823-10823 被引量:4
标识
DOI:10.1038/s41467-025-66131-x
摘要

The tremendous costs of disposal and potential environmental problems caused by waste catalysts bring about an urgent need for catalyst regeneration without loss of catalytic activity and stability. Here, we report on a simple and reproducible method to regenerate waste ozonation catalysts by carbonization of self-doped biological secretions to synthesize highly active and stable carbon-based nano-single-atom-site catalysts (NSASCs), Cu@graphitic carbon (GC)-Al2O3, converting waste catalysts into a sustainable resource. Specifically, Cu metal atoms are dispersed on the GC-Al2O3 composite support in the form of Cu1–C3 and Cun–Cun, primarily because the adsorption of biological secretions enhances the dispersibility of the metal nanoparticles. The pilot-scale demonstration reduces the average chemical oxygen demand (COD) of effluent in the Cu@GC-Al2O3/O3 system from 79.56 to 30.01 mg L−1, demonstrating enhanced catalytic activity and stability relative to the pristine fresh catalyst. The combined experimental and theoretical investigations reveal that the Cu1–C3 sites promote the formation of *Oad, while the Cun–Cun sites induce the generation of O2•− and 1O2 from *Oad, contributing to catalytic synergism in both radical and non-radical pathways. Additionally, the life cycle assessment confirms the economic feasibility and sustainability of the regeneration strategy. Our findings propose a general approach to reactivating waste catalysts, which can also inspire biological secretions in atom dispersal modulation and modification of other materials. Authors converted waste ozonation catalysts into carbon-based nano-single-atom-site catalysts through in-situ carbonization of self-doped biological secretions, enabling efficient regeneration and resource reuse.
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