化学
聚烯烃
催化作用
氢解
高分子科学
聚丙烯
有机化学
聚乙烯
纳米技术
材料科学
图层(电子)
作者
Jia‐Kai Sun,Jinhu Dong,Lijun Gao,Yu‐Quan Zhao,Hyunjin Moon,Susannah L. Scott
出处
期刊:Chemical Reviews
[American Chemical Society]
日期:2024-08-16
卷期号:124 (16): 9457-9579
被引量:1
标识
DOI:10.1021/acs.chemrev.3c00943
摘要
The large production volumes of commodity polyolefins (specifically, polyethylene, polypropylene, polystyrene, and poly(vinyl chloride)), in conjunction with their low unit values and multitude of short-term uses, have resulted in a significant and pressing waste management challenge. Only a small fraction of these polyolefins is currently mechanically recycled, with the rest being incinerated, accumulating in landfills, or leaking into the natural environment. Since polyolefins are energy-rich materials, there is considerable interest in recouping some of their chemical value while simultaneously motivating more responsible end-of-life management. An emerging strategy is catalytic depolymerization, in which a portion of the C-C bonds in the polyolefin backbone is broken with the assistance of a catalyst and, in some cases, additional small molecule reagents. When the products are small molecules or materials with higher value in their own right, or as chemical feedstocks, the process is called upcycling. This review summarizes recent progress for four major catalytic upcycling strategies: hydrogenolysis, (hydro)cracking, tandem processes involving metathesis, and selective oxidation. Key considerations include macromolecular reaction mechanisms relative to small molecule mechanisms, catalyst design for macromolecular transformations, and the effect of process conditions on product selectivity. Metrics for describing polyolefin upcycling are critically evaluated, and an outlook for future advances is described.
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