College of Science, Nanjing Agricultural University, Weigang street 1#, Nan Jing, 210095, China.
College of Science, Nanjing Agricultural University, Weigang street 1#, Nan Jing, 210095, China.
Environ Res. 2024 Dec 15;263(Pt 3):120249. doi: 10.1016/j.envres.2024.120249. Epub 2024 Oct 30.
Cobalt/iron bimetallic oxide coated with graphitized nitrogen-doped carbon (FeO-CoO@NC) was synthesized by convenient solid phase coordination combined with calcination method to activate PMS for the degradation of BSM. A series of Co/Fe bimetallic oxides with different metal ratios were designed and prepared to select the most efficient catalyst and FeO-CoO@NC(Co:Fe = 1:1) demonstrated the highest catalytic activity and the lowest ions leaching. The reasons for high catalytic activity of FeO-CoO@NC(Co:Fe = 1:1) were evaluated by a range of characterization techniques and the results showed it stemmed from higher mental content and larger current density. Complete (100%) degradation of 10 g L BSM was achieved within 10 min under the conditions of 0.05 g L catalyst and 0.3 mmol/L PMS dosage at 25 °C. Moreover, FeO-CoO@NC(Co:Fe = 1:1) showed more excellent catalytic activity and lower ions leaching than FeO, CoO and FeO-CoO, indicating superior bimetallic synergy and carbon encapsulation effect. Furtherly, radical experiments and XPS analysis revealed the main active species and catalytic mechanism of the FeO-CoO@NC/PMS system, respectively. Finally, the degradation pathway of BSM by FeO-CoO@NC/PMS system was deduced by LC-TOF-MS. This paper is aimed to provide a new insight into the convenient preparation method for the construction of catalysts which could reach efficient removal of complex organic pollutants.
钴/铁双金属氧化物负载石墨化氮掺杂碳(FeO-CoO@NC)通过简便的固相配位结合煅烧法合成,用于激活过一硫酸盐(PMS)降解 BSM。设计并制备了一系列不同金属比的 Co/Fe 双金属氧化物,以选择最有效的催化剂,结果表明 FeO-CoO@NC(Co:Fe=1:1)具有最高的催化活性和最低的离子浸出。通过一系列表征技术评估了 FeO-CoO@NC(Co:Fe=1:1)高催化活性的原因,结果表明这归因于更高的金属含量和更大的电流密度。在 25°C 下,催化剂用量为 0.05 g/L,过一硫酸盐(PMS)用量为 0.3 mmol/L 的条件下,10 min 内可完全(100%)降解 10 g/L 的 BSM。此外,FeO-CoO@NC(Co:Fe=1:1)比 FeO、CoO 和 FeO-CoO 具有更高的催化活性和更低的离子浸出,表明具有更好的双金属协同作用和碳包覆效应。进一步的自由基实验和 XPS 分析分别揭示了 FeO-CoO@NC/PMS 体系的主要活性物质和催化机制。最后,通过 LC-TOF-MS 推导出了 FeO-CoO@NC/PMS 体系降解 BSM 的途径。本文旨在为构建高效去除复杂有机污染物的催化剂提供一种简便的制备方法。