Department of Environmental Engineering & Innovation and Development Center of Sustainable Agriculture & Research Center of Sustainable Energy and Nanotechnology, National Chung Hsing University, 250 Kuo-Kuang Road, Taichung, Taiwan.
Department of Environment and Energy, Sejong University, 209 Neungdong-ro, Gunja-dong, Gwangjin-gu, Seoul, Republic of Korea.
Chemosphere. 2021 Mar;267:128906. doi: 10.1016/j.chemosphere.2020.128906. Epub 2020 Nov 9.
As salicylic acid (SAL) is increasingly consumed as a pharmaceutical product, release of SAL into the environment poses threats to ecology because of its low bio-degradability. Thus, SO-based chemical oxidation processes have been proposed for degrading SAL. Since monopersulfate (MPS) represents a primary reagent for generating SO, and Co is the most capable metal for activating MPS to generate SO, CO NPs are frequently proposed for activating MPS but they are difficult to recover from water. Thus CoFeO is considered as a magnetic alternative to CoO, and loading of CoFeO NPs on substrates could further improve dispersion and avoid aggregation of NPs. Therefore, this study proposes a 3-Dimensional (3D) hierarchical catalyst which is fabricated by loading CoFeO NPs on nitrogen-doped carbon sponge (NCS). The NCS is not only adopted as a support for CoFeO NPs but also provides additional catalytic sites and enhances catalytic activities of CoFeO NPs for MPS activation. As a result, CoFeO NPs loaded on NCS (CFNCS) exhibits substantially higher catalytic activities than CoFeO NPs and NCS individually with 100% of SAL could be afforded within 30 min. E of SAL degradation of 47.4 kJ/mol by CFNCS-activated MPS is also lower than those by other reported catalysts, whereas the RSE was 11.1%, which was also much higher than most of reported values. These features demonstrate that CFNCS is a promising 3D catalyst for enhancing MPS activation to degrade SAL. The findings obtained here are also insightful to develop efficient MPS-activating catalysts for eliminating contaminants.
由于水杨酸(SAL)作为一种医药产品的消耗量不断增加,其向环境中的释放对生态系统构成了威胁,因为它的生物降解性很低。因此,提出了基于过硫酸盐(SOP)的化学氧化工艺来降解 SAL。由于过一硫酸盐(MPS)代表生成 SO 的主要试剂,而 Co 是激活 MPS 生成 SO 的最有能力的金属,因此 Co NPs 经常被提议用于激活 MPS,但它们很难从水中回收。因此,CoFeO 被认为是 CoO 的磁性替代品,并且将 CoFeO NPs 负载在基底上可以进一步提高分散性并避免 NPs 的聚集。因此,本研究提出了一种由 CoFeO NPs 负载在氮掺杂碳海绵(NCS)上制备的 3 维(3D)分层催化剂。NCS 不仅被用作 CoFeO NPs 的载体,而且还提供了额外的催化位点,并提高了 CoFeO NPs 对 MPS 激活的催化活性。结果,负载在 NCS 上的 CoFeO NPs(CFNCS)表现出比 CoFeO NPs 和 NCS 本身更高的催化活性,在 30 分钟内可以实现 100%的 SAL 降解。CFNCS 激活的 MPS 对 SAL 的降解 E 为 47.4 kJ/mol,也低于其他报道的催化剂,而 RSE 为 11.1%,也高于大多数报道的值。这些特征表明,CFNCS 是一种有前途的 3D 催化剂,可用于增强 MPS 激活以降解 SAL。本研究的结果对于开发高效的 MPS 激活催化剂以去除污染物也具有启发性。