Light-assisted carbon dioxide reduction in an automated photoreactor system coupled to carbonylation chemistry

30 April 2024, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Continuous-flow methodologies offer promising avenues for sustainable processing due to their precise process control, scalability, and efficient heat and mass transfer. The small dimensions of continuous-flow reactors render them highly suitable for light-assisted reactions, as can be encountered in carbon dioxide hydrogenations. In this study, we present a novel reactor system emphasizing reproducibility, modularity, and automation, facilitating streamlined screening of conditions and catalysts for these processes. Through meticulous control over temperature, light intensity, pressure, residence time, and reagent stoichiometry, we conducted hydrogenation of carbon dioxide, yielding selective formation of carbon monoxide and methane using heterogeneous catalysts, including a newly developed ruthenium nanoparticle on titania catalyst. Furthermore, we demonstrated the direct utilization of on-demand generated carbon monoxide in the production of fine chemicals via various carbonylative cross-coupling reactions.

Keywords

photothermal catalysis
automation
continuous flow
solar chemistry
CO2 valorization

Supplementary materials

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Description
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SI
Description
experimental procedures, setup details, molecular characterization
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