4.8 Article

Towards highly efficient continuous-flow catalytic carbon dioxide cycloadditions with additively manufactured reactors

期刊

GREEN CHEMISTRY
卷 24, 期 8, 页码 3300-3308

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1gc04593h

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资金

  1. Pla de Promocio de la Investigacio de la Universitat Jaume I [UJI-B2019-40, UJI-B2020-44]
  2. FEDER//Ministerio de Ciencia e Innovacion - Agencia Estatal de Investigacion [RTI2018-098233-B-C22 y C21]
  3. UNED (Costa Rica)
  4. European Union [101026335]
  5. Generalitat Valenciana [CIDEGENT 2018/036]
  6. Marie Curie Actions (MSCA) [101026335] Funding Source: Marie Curie Actions (MSCA)

向作者/读者索取更多资源

Developing efficient and sustainable methods to convert CO2 into valuable chemicals is crucial for decarbonization in the chemical industry. In this study, a novel multi-scale approach combining hydrogen bonding ability, metal-free catalysts, and supported ionic liquids on polymers was developed for the cycloaddition of CO2 to epoxides. The use of additive manufacturing allowed for the digital design and rapid fabrication of structured reactors, which showed higher catalytic activity compared to packed bed reactors of similar size.
Developing efficient and sustainable methodologies to transform CO2 into added-value chemicals is an important strategy for decarbonization in the chemical industry. Here, a new multi-scale approach for the cycloaddition of CO2 to epoxides is reported, designed by combining the hydrogen bonding ability, metal-free catalysts and supported ionic liquids on polymers. The use of additive manufacturing (AM) techniques allowed the digital design and rapid fabrication of structured architectures for continuous-flow reactors, which offers potential for process optimization. AM generated catalytic reactors showed higher catalytic activity than similar sized packed bed reactors, when normalised to the amount of catalyst and their surface area. The catalytic activity and stability were maintained over a prolonged period of time (300 h) without loss of activity, and it was demonstrated to efficiently transform a range of epoxide substrates.

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