Yukai Jiang, Bo Feng, Yingxiu Gao, Xiaohui Liu, Yanqin Wang
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引用次数: 0
Abstract
Polyamide 6 (PA6) is a kind of engineering plastic containing N atoms, the low activity of amide linkage makes it hard to recycle under mild conditions. In this work, a solid acid catalyst, L-Nb2O5 is applied to convert PA6 into ε-caprolactam and as high as 82.2 % yield was achieved at 260°C, a relatively low temperature with THF as solvent. The catalyst can be used for 5 times with little decline of catalytic activity, and can be regenerated through calcination. Catalytic mechanism investigation reveals that Lewis acidity rather than acid concentration plays a decisive role in depolymerization, whereas Brönsted acid sites exhibit an inhibitory effect on the process. Enhanced specific surface area facilitates the exposure of more acidic sites, thereby promoting depolymerization efficiency. Systematic cyclic stability assessments and scaled-up experiments confirm the system's robustness and practical viability for industrial implementation. This study ultimately establishes a facile and efficient methodology for achieving closed-loop recycling of polyamide 6 (PA6) to ε-caprolactam (CPL) through rational catalyst design.
期刊介绍:
Catalysis Today focuses on the rapid publication of original invited papers devoted to currently important topics in catalysis and related subjects. The journal only publishes special issues (Proposing a Catalysis Today Special Issue), each of which is supervised by Guest Editors who recruit individual papers and oversee the peer review process. Catalysis Today offers researchers in the field of catalysis in-depth overviews of topical issues.
Both fundamental and applied aspects of catalysis are covered. Subjects such as catalysis of immobilized organometallic and biocatalytic systems are welcome. Subjects related to catalysis such as experimental techniques, adsorption, process technology, synthesis, in situ characterization, computational, theoretical modeling, imaging and others are included if there is a clear relationship to catalysis.