4.6 Article

Metal-Free N-Doped Carbons for Solvent-Less CO2 Fixation Reactions: A Shrimp Shell Valorization Opportunity

期刊

ACS SUSTAINABLE CHEMISTRY & ENGINEERING
卷 10, 期 41, 页码 13835-13848

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acssuschemeng.2c04443

关键词

metal-free; N-doped carbons; chitin; chitosan; shrimp shells; CO2 insertion; cyclic carbonates; continuous flow

资金

  1. Ministrerio de Ciencia e Innovacion [PID2021-126235OB-C32]
  2. Junta de Andalucia [UMA18-FEDERJA-126]
  3. FEDER funds

向作者/读者索取更多资源

In this study, metal-free nitrogen-doped carbon catalysts obtained from chitosan, chitin, and shrimp shell wastes were used for the synthesis of organic cyclic carbonates from CO2. The catalysts showed good stability and reusability, with ca. (75 +/- 3)% of the initial conversion achieved/retained after six recycles.
High anthropogenic CO2 emissions are among the main causes of climate change. Herein, we investigate the use of CO2 for the synthesis of organic cyclic carbonates on metal-free nitrogen-doped carbon catalysts obtained from chitosan, chitin, and shrimp shell wastes, both in batch and in continuous flow (CF). The catalysts were characterized by N-2 physisorption, CO2-temperature-programmed desorption, X-ray photoelectron spectroscopy, scanning electron microscopy, and CNHS elemental analysis, and all reactivity tests were run in the absence of solvents. Under batch conditions, the catalyst obtained by calcination of chitin exhibited excellent performance in the conversion of epichlorohydrin (selected as a model epoxide), resulting in the corresponding cyclic carbonate with 96% selectivity at complete conversion, at 150 degrees C and 30 bar CO2, for 4 h. On the other hand, in a CF regime, a quantitative conversion and a carbonate selectivity >99% were achieved at 150 degrees C, by using the catalyst obtained from shrimp waste. Remarkably, the material displayed an outstanding stability over a reaction run time of 180 min. The robustness of the synthetized catalysts was confirmed by their good operational stability and reusability: ca. (75 +/- 3)% of the initial conversion was achieved/retained by all systems, after six recycles. Also, additional batch experiments proved that the catalysts were successful on different terminal and internal epoxides.

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