Electrochemistry-assisted selective butadiene hydrogenation with water

Yong Qing Yan, Ya Chen, Zhao Wang, Li Hua Chen, Hao Lin Tang, Bao Lian Su

Résultats de recherche: Contribution à un journal/une revueArticleRevue par des pairs

Résumé

Alkene feedstocks are used to produce polymers with a market expected to reach 128.4 million metric tons by 2027. Butadiene is one of the impurities poisoning alkene polymerization catalysts and is usually removed by thermocatalytic selective hydrogenation. Excessive use of H2, poor alkene selectivity and high operating temperature (e.g. up to 350 °C) remain the most significant drawbacks of the thermocatalytic process, calling for innovative alternatives. Here we report a room-temperature (25~30 °C) electrochemistry-assisted selective hydrogenation process in a gas-fed fixed bed reactor, using water as the hydrogen source. Using a palladium membrane as the catalyst, this process offers a robust catalytic performance for selective butadiene hydrogenation, with alkene selectivity staying around 92% at a butadiene conversion above 97% for over 360 h of time on stream. The overall energy consumption of this process is 0.003 Wh/mLbutadiene, which is thousands of times lower than that of the thermocatalytic route. This study proposes an alternative electrochemical technology for industrial hydrogenation without the need for elevated temperature and hydrogen gas.

langue originaleAnglais
Numéro d'article2106
journalNature Communications
Volume14
Numéro de publication1
Les DOIs
Etat de la publicationPublié - déc. 2023

Financement

This work was supported by the Program of Introducing Talents of Discipline to Universities-Plan 111 (B0002) from the Ministry of Science and Technology and the Ministry of Education of China. We thank the National Natural Science Foundation of China (grant 21902122, 22293020, and 22293022), the National Key R&D Program of China (grant 2021YFE0115800), the Postdoctoral Science Foundation of China (grant 2019M652723) and Foshan Xianhu Laboratory of the Advanced Energy Science and Technology Guangdong Laboratory (XHD2020-002). We thank Professor Jun-Sheng Li for providing the utilization permission of VASP resource. The work was carried out at LvLiang Cloud Computing Center of China, and the calculations were performed on TianHe-2. We thank Professor Hazar Guesmi for her advice on DFT calculation and analyzation and Professor Catherine Louis for her advice on catalytic results analyzation.

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