Enhancing Organic Electrosynthesis through Artificial Intelligence: The Case of Adiponitrile Electrohydrodimerization

作者
Daniela Eugenia Blanco,Bryan E. J. Lee,Miguel Antonio Modestino
出处
期刊:Meeting abstracts [Institute of Physics]
卷期号:MA2019-02 (44): 2048-2048
标识
DOI:10.1149/ma2019-02/44/2048
摘要

The continuous increase of fossil fuel-derived carbon dioxide (CO2) emissions has made their impact in climate change self-evident. The chemical industry is a major contributor to this increase, accounting for more than 5.5% of the global CO2 emissions. The electrification of the chemical industry would thus be a major step in the integration of renewable electricity in the industrial sector, helping reduce its carbon footprint significantly. Inorganic electrosynthetic processes have been largely implemented at industrial scale (i.e. chloro-alkali and Aluminum production), however the deployment of electrosynthetic methods for the production of organic chemicals has been limited. Adiponitrile (ADN) is a large-volume (>1.5 million tons/year) precursor to Nylon 6,6 and it can be obtained via the electrohydrodimerization of acrylonitrile (AN). Although the electrochemical production of adiponitrile (ADN) is the largest organic electrochemical process in industry, it faces many challenges owing mainly to its energy conversion efficiency and selectivity. Optimizing the composition of the electrolyte has resulted in significant performance improvements, however mass transport limitations have proven to be a challenge at high current densities, where propionitrile (PN) is the main reaction by-product. In this study, we provide experimental insights on the effects of pulsed potential techniques on the mitigation of mass transport limitations and the effective control of product distribution. Moreover, an integrated approach combining experimental insights and artificial intelligence-driven models is proposed for the rapid optimization of operation conditions and the maximization of reaction performance. The regulation of electron-transfer rates with the use of complex pulse potential waveforms is implemented to control the electrochemical environment surrounding the reaction surface, ultimately favoring ADN production. Electrochemical pulses are used to balance reactant diffusive fluxes to the electrode and the generation/consumption of species in the electrical double layer (EDL), helping mitigate mass transport limitations at high current densities. This, together with their effect on interaction between electroactive species and the reaction surface can help improve reaction selectivity. An improvement of over 250% in the production ratio of ADN:PN (desired to undesired product) was achieved optimizing pulse duration and amplitude. Furthermore, the careful control of overall reaction time and composition of the EDL led to a 20% increase in ADN production with respect to DC operation. The integrated use of machine learning algorithms enabled the prediction of ADN formation in a complete landscape of pulse durations. From this, a new set of optimal conditions was identified, leading to a 30% increase in ADN production with respect to DC operation for periodic pulses varying from -60 mA cm-2 (120 ms) to 0 mA cm-2 (5 ms). A new paradigm in organic electrosynthesis research is proposed, where a combination of electrochemical design principles, artificial neural networks, and judiciously designed experimental campaigns are used to uncover new electrosynthetic processes.

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