Institute of Environmental Science, School of Environmental and Resources Sciences, Shanxi University, 030006, China.
Shanxi Laboratory for Yellow River, Taiyuan 030006, China.
Dalton Trans. 2024 Jun 17;53(24):10189-10200. doi: 10.1039/d4dt00758a.
The accumulation of tetracycline hydrochloride (TCH) threatens human health because of its potential biological toxicity. Carbon -based materials with easy isolation and excellent performance that can activate peroxymonosulfate (PMS) to generate reactive oxygen species for TCH degradation are essential, but the development of such materials remains a significant challenge. In this study, based on the idea of treating waste, tricobalt tetraoxide loaded P-doped biochar (Co NP-PBC) was synthesised to activate PMS for the degradation of TCH. Possible degradation pathways and intermediate products of TCH were identified using High performance liquid chromatography tandem mass spectrometry (HPLC-MS) detection and density functional theory analysis. Toxicity analysis software was used to predict the toxicity of the intermediate products. Compared to catalysts loaded with Fe and Mn and other Co-based catalysts, Co NP-PBC exhibited an optimal performance (with a kinetic constant of 0.157 min for TCH degradation), and over 99.0% of TCH can be degraded within 20 min. This mechanism demonstrates that the non-free radical oxidation of O plays a major role in the degradation of TCH. This study provides insights into the purification of wastewater using BC-based catalysts.
盐酸四环素(TCH)的积累对人类健康构成威胁,因为其具有潜在的生物毒性。能够激活过一硫酸盐(PMS)生成用于 TCH 降解的活性氧的、易于分离且性能优异的碳基材料至关重要,但此类材料的开发仍然是一个重大挑战。在本研究中,基于废物处理的理念,制备了负载三氧化二钴的 P 掺杂生物炭(Co NP-PBC)来激活 PMS 以降解 TCH。使用高效液相色谱串联质谱(HPLC-MS)检测和密度泛函理论分析鉴定了 TCH 的可能降解途径和中间产物。使用毒性分析软件预测了中间产物的毒性。与负载 Fe 和 Mn 的催化剂以及其他基于 Co 的催化剂相比,Co NP-PBC 表现出最佳的性能(TCH 降解的动力学常数为 0.157 min),在 20 min 内可以降解超过 99.0%的 TCH。该机制表明,O 的非自由基氧化在 TCH 的降解中起主要作用。本研究为使用基于 BC 的催化剂净化废水提供了思路。