College of Resources and Environment, Chengdu University of Information Technology, Chengdu, Sichuan 610225, China.
College of Resources and Environment, Chengdu University of Information Technology, Chengdu, Sichuan 610225, China.
Ecotoxicol Environ Saf. 2024 Oct 15;285:117126. doi: 10.1016/j.ecoenv.2024.117126. Epub 2024 Oct 5.
Heterogeneous catalyst-mediated sulfate radical-based advanced oxidation processes (SR-AOPs) showed excellent performance during antibiotics degradation. Spinel was a promising catalyst for SR-AOPs, but the secondary contamination due to metal ions leaching needed to be addressed. And the destruction of catalyst structure could lead to the reduction of catalytic activity and the difficulty of recovery. Thus, a novel nitrogen-doped carbon (NC)-supported CoFeO (CoFeO@NC) was synthesized as the activator of PMS for sulfadiazine (SDZ) degradation under low Co leaching conditions. The consequences indicated that the CoFeO@NC/PMS system exhibited higher PMS decomposition efficiency and reaction stoichiometry efficiency than the bare CoFeO/PMS systems (CoFeO-180 and CoFeO-800), which in turn demonstrated a better SDZ removal performance. Under the condition of CoFeO@NC dosage 0.1 g/L, PMS concentration 0.5 mM, solution pH 6.8 and temperature 25°C, SDZ (20 mg/L) was almost completely degraded within 60 min. XPS analysis showed that the NC not only protected and stabilized CoFeO, but also provided additional active sites for PMS activation. During SDZ degradation, SO, HO, O and O were involved in the reaction, among which SO and HO made the main contribution. Meanwhile, CoFeO@NC could be recovered by magnetic separation, and showed great stability (Co leaching 0.852 mg/L) and reusability. In the fifth cycle experiment, 85.02 % SDZ degradation was obtained. Based on the detected intermediates (12 intermediates were identified) and DFT calculations, possible degradation pathways for SDZ in CoFeO@NC/PMS were proposed. The condensed dual descriptor indicated that the N7, N11, and C15 atoms on SDZ molecule were the main sites of electrophilic attack, which was consistent with the detected intermediates. The degradation of SDZ involved hydroxylation of NH, cleavage of S-N and extrusion of SO. This study explored the improvements made in NC support material to catalytic performance and resistance to dissolution of spinel, providing new insights for subsequent researches.
基于硫酸盐自由基的高级氧化工艺(SR-AOPs)中的多相催化剂在抗生素降解方面表现出优异的性能。尖晶石是 SR-AOPs 的一种有前途的催化剂,但需要解决金属离子浸出引起的二次污染问题。而且,催化剂结构的破坏会导致催化活性的降低和回收的困难。因此,一种新型的氮掺杂碳(NC)负载的 CoFeO(CoFeO@NC)被合成出来,作为 PMS 的活化剂,用于在低 Co 浸出条件下降解磺胺嘧啶(SDZ)。结果表明,与裸 CoFeO/PMS 体系(CoFeO-180 和 CoFeO-800)相比,CoFeO@NC/PMS 体系具有更高的 PMS 分解效率和反应计量效率,从而表现出更好的 SDZ 去除性能。在 CoFeO@NC 用量为 0.1 g/L、PMS 浓度为 0.5 mM、溶液 pH 值为 6.8 和温度为 25°C 的条件下,20 mg/L 的 SDZ 在 60 min 内几乎完全降解。XPS 分析表明,NC 不仅保护和稳定了 CoFeO,而且为 PMS 的活化提供了额外的活性位点。在 SDZ 降解过程中,SO、HO、O 和 O 参与了反应,其中 SO 和 HO 起主要作用。同时,CoFeO@NC 可以通过磁分离回收,具有良好的稳定性(Co 浸出率为 0.852 mg/L)和可重复使用性。在第五次循环实验中,SDZ 的降解率达到了 85.02%。根据检测到的中间产物(鉴定出 12 种中间产物)和 DFT 计算,提出了 CoFeO@NC/PMS 中 SDZ 的可能降解途径。凝聚双描述符表明,SDZ 分子上的 N7、N11 和 C15 原子是亲电攻击的主要位点,与检测到的中间产物一致。SDZ 的降解涉及 NH 的羟化、S-N 的断裂和 SO 的排出。本研究探索了 NC 支撑材料对尖晶石催化性能和抗溶解性能的改进,为后续研究提供了新的见解。