Synthesis of single atom cobalt dispersed on 2D carbon nanoplate and degradation of acetaminophen by peroxymonosulfate activation

催化作用 化学 X射线光电子能谱 降级(电信) 核化学 无机化学 化学工程 碳纤维 材料科学 有机化学 计算机科学 电信 复合数 工程类 复合材料
作者
Gaozu Liao,Xiaojiao Qing,Peng Xu,Laisheng Li,Ping Lü,Weirui Chen,Dehua Xia
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:427: 132027-132027 被引量:59
标识
DOI:10.1016/j.cej.2021.132027
摘要

Single Co atoms dispersed on 2D carbon nanoplate catalyst (SA-Co CNP) was synthesized successfully by a facile one-step method. Its morphology and structure were characterized by SEM, TEM, HAADF-STEM, XRD and XPS. Results showed that SA-Co CNP exbibit uniform two-dimensional nanoplate structure with several micrometers. Co was single atomic dispersed in carbon skeleton with the form of CoN4 coordination. The kinetic constant of acetaminophen (APAP) degradation with 0.1% SA-Co CNP/PMS was 6.99 times and 1.24 times as great as that of conventional CoOx-CNP/PMS and Co2+/PMS process, respectively. APAP could be efficiently degraded in a wide pH range of 3 to 9. The presence of Cl− could enhance the removal of APAP, while HCO3–, HPO4− and humic acid inhibit APAP degradation. The results of cyclic test demonstrated that 0.1% SA-Co CNP owns excellent catalytic ability and stability for PMS activation in a wide pH range of 3–9. Additionally, the reaction mechanism for APAP degradation by 0.1% SA-Co CNP/PMS was explored using ESR and trapping experiments. 1O2 was proved to be the predominant ROS. Hydroquinone was detected as the intermediate by LC-MS technique and a possible pathway for APAP removal was proposed. Finally, the degradation of APAP in real water matrix were investigated. The results showed that 0.1% SA-Co CNP/PMS not only possessed good performance for APAP degradation in tap water and surface water, but also could improve the biodegradability for secondary biochemical effluent.
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