Suppr超能文献

由一氧化碳、氧气和水开始的过甲酸的全电化学合成。

All Electrochemical Synthesis of Performic Acid Starting from CO, O, and HO.

作者信息

Dinges Ida, Pyschik Markus, Schütz Julian, Schneider Selina, Klemm Elias, Waldvogel Siegfried R, Stöckl Markus

机构信息

Chemical Technology, DECHEMA Research Institute, Theodor-Heuss-Allee 25, 60486, Frankfurt am Main, Germany.

Department for Electrosynthesis, Max Planck Institute for Chemical Energy Conversion, Stiftstraße 34-36, 45470, Mülheim an der Ruhr, Germany.

出版信息

ChemSusChem. 2025 Jun 17;18(12):e202500180. doi: 10.1002/cssc.202500180. Epub 2025 Apr 23.

Abstract

Driven by anthropogenic climate change, innovative approaches to defossilize the chemical industry are required. Herein, the first all-electrochemical feasibility study for the complete electrosynthesis of the strong oxidizer and effective disinfectant performic acid is presented. Its synthesis is achieved solely from CO, O, and HO in a two-step process. Initially, CO is electrochemically reduced to formate employing BiO-based gas diffusion electrodes in a phosphate-buffered electrolyte. Thereby, high formate concentration (500.7 ± 0.6 mmol L) and high Faradaic efficiency (86.3 ± 0.3%) are achieved at technically relevant current density (150 mA cm). Subsequently, the formate acts as (storable) feed electrolyte for the second electrolysis step. Employing carbon-based gas diffusion electrodes, O is reduced to HO and performic acid is directly formed in situ. As before, high HO concentration (1.27 ± 0.06 mol L) and high Faradaic efficiency (85.3 ± 5.4%) are achieved. Furthermore, performic acid concentration suitable for disinfection is obtained (82 ± 11 mmol L). In summary, this innovative feasibility study highlights the potential of combining electrochemical CO reduction with HO electrosynthesis, which could provide sustainable access to performic acid in the future.

摘要

在人为气候变化的推动下,需要创新方法使化学工业摆脱化石燃料的依赖。在此,首次提出了关于强氧化剂和有效消毒剂过甲酸完全电合成的全电化学可行性研究。其合成仅通过两步过程由一氧化碳、氧气和水实现。首先,在磷酸盐缓冲电解质中使用基于氧化铋的气体扩散电极将一氧化碳电化学还原为甲酸盐。由此,在技术相关电流密度(150 mA/cm²)下实现了高甲酸盐浓度(500.7±0.6 mmol/L)和高法拉第效率(86.3±0.3%)。随后,甲酸盐作为第二步电解的(可储存)进料电解质。使用碳基气体扩散电极,氧气被还原为过氧化氢,过甲酸直接原位形成。和之前一样,实现了高过氧化氢浓度(1.27±0.06 mol/L)和高法拉第效率(85.3±5.4%)。此外,还获得了适合消毒的过甲酸浓度(82±11 mmol/L)。总之,这项创新的可行性研究突出了将电化学一氧化碳还原与过氧化氢电合成相结合的潜力,这有望在未来为过甲酸提供可持续的获取途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8ef/12175041/090e4f25168e/CSSC-18-e202500180-g005.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验