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在 CoO 阳极中引入亲电 Cu(II)以增强 •Cl 生成,用于在尿液处理中高效去除总氮并回收氢气。

Enhanced •Cl generation by introducing electrophilic Cu(II) in CoO anode for efficient total nitrogen removal with hydrogen recovery in urine treatment.

机构信息

School of Environmental Science and Engineering, Key Laboratory of Thin Film and Microfabrication Technology (Ministry of Education), Shanghai Jiao Tong University, Shanghai 200240, China.

School of Environmental Science and Engineering, Key Laboratory of Thin Film and Microfabrication Technology (Ministry of Education), Shanghai Jiao Tong University, Shanghai 200240, China.

出版信息

Water Res. 2024 Jan 1;248:120847. doi: 10.1016/j.watres.2023.120847. Epub 2023 Nov 7.

Abstract

Urine is a nitrogen-containing waste, but can be used as an attractive alternative substrate for H recovery. However, conventional urea oxidation reaction is subject to complex six-electron transfer kinetics and requires alkaline conditions. Herein, an efficient method of enhancing •Cl generation by introducing electrophilic Cu(II) into CoO nanowires anode was proposed, which realized the highly efficient TN removal and H production in urine treatment under neutral conditions. The key mechanism is that the electrophilic effect of Cu(II) attracts electrons from the oxygen atom, which causes the oxygen atom to further attract electrons from Co(II), reducing the charge density of Co(II). Electrophilic Cu(II) accelerates the difficult conversion step of Co(II) to Co(III), which enhances the generation of •Cl. The generated •Cl efficiently converts urea to N, while the electron transport promotes H production on the CuO@CF nanowires cathode. Results showed that the steady-state concentration of •Cl was increased to about 1.5 times by the Cu(II) introduction. TN removal and H production reached 94.7% and 642.1 μmol after 50 min, which was 1.6 times and 1.5 times that of CoO system, respectively. It was also 2.3 times and 2.1 times of RuO, and 3.3 times and 2.5 times of Pt, respectively. Moreover, TN removal was 11.0 times higher than that of without •Cl mediation, and H production was 4.3 times higher. More importantly, excellent TN removal and H production were also observed in the actual urine treatment. This work provides a practical possibility for efficient total nitrogen removal and hydrogen recovery in urine wastewater treatment.

摘要

尿液是一种含氮废物,但可以作为回收 H 的有吸引力的替代底物。然而,传统的尿素氧化反应受到复杂的六电子转移动力学和需要碱性条件的限制。在此,提出了一种通过将亲电 Cu(II) 引入 CoO 纳米线阳极来增强 •Cl 生成的有效方法,该方法在中性条件下实现了高效的 TN 去除和尿液处理中的 H 生产。关键机制是 Cu(II)的亲电性从氧原子吸引电子,导致氧原子进一步从 Co(II)吸引电子,降低 Co(II)的电荷密度。亲电 Cu(II)加速 Co(II)向 Co(III)的困难转化步骤,从而增强了 •Cl 的生成。生成的 •Cl 有效地将尿素转化为 N,而电子传递则促进 CuO@CF 纳米线阴极上的 H 生产。结果表明,Cu(II)的引入将 •Cl 的稳态浓度提高到约 1.5 倍。TN 去除和 H 生产在 50 分钟后分别达到 94.7%和 642.1 μmol,分别是 CoO 体系的 1.6 倍和 1.5 倍,分别是 RuO 的 2.3 倍和 2.1 倍,分别是 Pt 的 3.3 倍和 2.5 倍。此外,没有 •Cl 介导时的 TN 去除率提高了 11.0 倍,H 产量提高了 4.3 倍。更重要的是,实际尿液处理中也观察到了出色的 TN 去除和 H 生产。这项工作为尿液废水处理中高效总氮去除和氢气回收提供了实际可能性。

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