Interactions between atomically dispersed copper and phosphorous species are key for the hydrochlorination of acetylene

Vinyl chloride, the monomer of polyvinyl chloride (PVC), is industrially synthesized via acetylene hydrochlorination. Thereby, easy to sublimate but toxic mercury chloride catalysts are widely used. It is imperative to find environmentally friendly non-mercury catalysts to promote the green producti...

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Veröffentlicht in:Communications chemistry 2022-01, Vol.5 (1), p.2-10, Article 2
Hauptverfasser: Wang, Ting, Jiang, Zhao, Tang, Qi, Wang, Bolin, Wang, Saisai, Yu, Mingde, Chang, Renqin, Yue, Yuxue, Zhao, Jia, Li, Xiaonian
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Sprache:eng
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Zusammenfassung:Vinyl chloride, the monomer of polyvinyl chloride (PVC), is industrially synthesized via acetylene hydrochlorination. Thereby, easy to sublimate but toxic mercury chloride catalysts are widely used. It is imperative to find environmentally friendly non-mercury catalysts to promote the green production of PVC. Low-cost copper-based catalysts are promising candidates. In this study, phosphorus-doped Cu-based catalysts are prepared. It is shown that the type of phosphorus configuration and the distribution on the surface of the carrier can be adjusted by changing the calcination temperature. Among the different phosphorus species, the formed P-C bond plays a key role. The coordination structure formed by the interaction between P-C bonds and atomically dispersed Cu 2+ species results in effective and stable active sites. Insights on how P-C bonds activate the substrate may provide ideas for the design and optimization of phosphorus-doped catalysts for acetylene hydrochlorination. Copper-based catalysts are widely investigated for the industrially important hydrochlorination of acetylene (PVC production), whereby phosphorus-doped carbon supports have been found to improve the catalyst’s properties. Here the interaction between the P-C bond and atomically dispersed Cu 2+ species is clarified and the reaction path of C 2 H 2 and HCl revealed.
ISSN:2399-3669
2399-3669
DOI:10.1038/s42004-021-00619-7