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氮掺杂碳纳米管作为无金属催化剂用于过氧乙酸活化降解新兴污染物:反应机理探索与活性位点预测

N-doped carbon nanotubes as metal-free catalysts for PAA activation to degrade emerging pollutants: Exploration of reaction mechanisms and prediction of active sites.

作者信息

Shi Miao, Zhang Bin, Yan Xiaoyu, Ma Jun, He Xu

机构信息

State Key Laboratory of Urban Water Resource and Environment, School of Environment, Harbin Institute of Technology, Harbin, 150090, China.

State Key Laboratory of Urban Water Resource and Environment, School of Environment, Harbin Institute of Technology, Harbin, 150090, China.

出版信息

Environ Res. 2025 Oct 1;282:121998. doi: 10.1016/j.envres.2025.121998. Epub 2025 May 29.

DOI:10.1016/j.envres.2025.121998
PMID:40449576
Abstract

In this study, we utilized urea as a nitrogen precursor and synthesized a series of nitrogen-doped carbon nanotubes with varying catalytic activities for PAA by adjusting the mass ratio of urea to carbon nanotubes (ranging from 0.01:1 to 2:1) and the preparation temperature (between 400 °C and 1000 °C). The activation mechanism was thoroughly examined through extensive characterization and calculations. During the activation process with PAA, we observed that the removal of contaminants was linearly correlated with the extent of graphitization (R = 0.873) and the degree of nitrogen doping (R = 0.951). These findings were further corroborated by density functional theory (DFT) calculations. Different types of nitrogen atoms can reduce the peroxide-breaking energy barrier in PAA to varying degrees, thereby facilitating the conversion of NCNT-PAA∗ complexes into adsorbed hydroxyl radicals. The system achieves an impressive 100 % oxidative removal of 20 μM micropollutants (e.g., bisphenol A) within 60 min, thanks to the synergistic effects of electron transfer and radical adsorption. Furthermore, it maintains a remarkable micropollutant removal efficiency of nearly 80 % after five consecutive uses. Additionally, carbon materials can be effectively integrated with membrane filtration, which not only facilitates the recycling of carbon materials in practical applications but also enhances the catalytic efficiency of nitrogen-doped multi-walled carbon nanotubes (NCNTs) while ensuring the safety of the effluent. These results underscore the extensive application prospects and research potential of carbon-based materials, while also providing a novel approach for the advanced oxidation technology of PAA.

摘要

在本研究中,我们以尿素作为氮前驱体,通过调整尿素与碳纳米管的质量比(范围为0.01:1至2:1)以及制备温度(400℃至1000℃之间),合成了一系列对过氧乙酸(PAA)具有不同催化活性的氮掺杂碳纳米管。通过广泛的表征和计算对活化机制进行了深入研究。在用PAA进行活化过程中,我们观察到污染物的去除与石墨化程度(R = 0.873)和氮掺杂程度(R = 0.951)呈线性相关。密度泛函理论(DFT)计算进一步证实了这些发现。不同类型的氮原子可不同程度地降低PAA中过氧化物分解的能垒,从而促进NCNT - PAA∗络合物转化为吸附的羟基自由基。由于电子转移和自由基吸附的协同作用,该体系在60分钟内可实现对20μM微污染物(如双酚A)高达100%的氧化去除。此外,连续使用五次后,其仍保持近80%的显著微污染物去除效率。此外,碳材料可有效地与膜过滤相结合,这不仅便于碳材料在实际应用中的循环利用,还能提高氮掺杂多壁碳纳米管(NCNTs)的催化效率,同时确保出水安全。这些结果凸显了碳基材料广阔的应用前景和研究潜力,同时也为PAA的高级氧化技术提供了一种新方法。

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