通过二氧化碳硝酸盐还原和甘油氧化连续流电合成尿素和草酸

IF 15.7 1区 化学 Q1 CHEMISTRY, APPLIED
Shuanglong Zhou, Yue Shi, Yu Dai, Tianrong Zhan, Jianping Lai, Lei Wang
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引用次数: 0

摘要

尿素和草酸是各种化学制造业的关键成分。然而,在连续流电解槽中同时生成尿素和草酸是一项挑战。在此,我们报告了一种配备了 9 平方厘米有效面积气体扩散电极(GDE)的连续流电解槽,该电极可在阳极区同时催化甘油氧化反应,在阴极区同时催化二氧化碳和硝酸盐的还原反应,从而在阳极和阴极分别生成草酸和尿素。低电池电压(0.9 V)下的电流密度在连续 10 个电解循环(共 120 小时)中都保持在 18.7 mA cm-2 以上,草酸(67.1%)和尿素(70.9%)的法拉第效率没有衰减。实验和理论研究表明,在阴极 C-N 键的形成方面,Pd-sites 能为 CO2 和 NO3- 的氢化过程提供质子,Cu-sites 能促进 *COOH 的生成,Bi-sites 能稳定 *COOH。此外,就甘油氧化而言,在钯金属中引入 Cu 和 Bi 可分别促进甘油分子中羟基的氧化和 C-C 键的裂解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Continuous-flow electrosynthesis of urea and oxalic acid by CO2-nitrate reduction and glycerol oxidation

Urea and oxalic acid are critical component in various chemical manufacturing industries. However, achieving simultaneous generation of urea and oxalic acid in a continuous-flow electrolyzer is a challenge. Herein, we report a continuous-flow electrolyzer equipped with 9-square centimeter-effective area gas diffusion electrodes (GDE) which can simultaneously catalyze the glycerol oxidation reaction in the anode region and the reduction reaction of CO2 and nitrate in the cathode region, producing oxalic acid and urea at both the anode and cathode, respectively. The current density at low cell voltage (0.9 V) remained above 18.7 mA cm–2 for 10 consecutive electrolysis cycles (120 h in total), and the Faraday efficiency of oxalic acid (67.1%) and urea (70.9%) did not decay. Experimental and theoretical studies show that in terms of the formation of C–N bond at the cathode, Pd-sites can provide protons for the hydrogenation process of CO2 and NO3, Cu-sites can promote the generation of *COOH and Bi-sites can stabilize *COOH. In addition, in terms of glycerol oxidation, the introduction of Cu and Bi into Pd metallene promotes the oxidation of hydroxyl groups and the cleavage of C–C bond in glycerol molecules, respectively.

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来源期刊
Chinese Journal of Catalysis
Chinese Journal of Catalysis 工程技术-工程:化工
CiteScore
25.80
自引率
10.30%
发文量
235
审稿时长
1.2 months
期刊介绍: The journal covers a broad scope, encompassing new trends in catalysis for applications in energy production, environmental protection, and the preparation of materials, petroleum chemicals, and fine chemicals. It explores the scientific foundation for preparing and activating catalysts of commercial interest, emphasizing representative models.The focus includes spectroscopic methods for structural characterization, especially in situ techniques, as well as new theoretical methods with practical impact in catalysis and catalytic reactions.The journal delves into the relationship between homogeneous and heterogeneous catalysis and includes theoretical studies on the structure and reactivity of catalysts.Additionally, contributions on photocatalysis, biocatalysis, surface science, and catalysis-related chemical kinetics are welcomed.
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