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Co3O4 nanocube-decorated nitrogen-doped carbon foam as an enhanced 3-dimensional hierarchical catalyst for activating Oxone to degrade sulfosalicylic acid

机译:Co3O4纳米棉装饰的氮气碳泡沫作为增强的三维等级催化剂,用于激活氧化的氧化力降解硫磺酸琥珀酸

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As sulfosalicylic acid (SUA) is extensively used as a pharmaceutical product, discharge of SUA into the environment becomes an emerging environmental issue because of its low bio-degradability. Thus, SO4 center dot--based advanced oxidation processes have been proposed for degrading SUA because of many advantages of SO4 center dot-. As Oxone represents a dominant reagent for producing SO4 center dot-, and Co is the most capable metal for activating Oxone to generate SO4 center dot-, it is critical to develop an effective but easy-to-use Co-based catalysts for Oxone activation to degrade SUA. Herein, a 3D hierarchical catalyst is specially created by decorating Co3O4 nanocubes (NCs) on macroscale nitrogen-doped carbon form (NCF). This Co3O4-decorated NCF (CONCF) is free-standing, macroscale and even squeezable to exhibit interesting and versatile features. More importantly, CONCF consists of Co3O4 NCs evenly distributed on NCF without aggregation. The NCF not only serves as a support for Co3O4 NCs but also offers additional active sites to synergistically enhance catalytic activities towards Oxone activation. Therefore, CONCF exhibits a higher catalytic activity than the conventional Co3O4 nanoparticles for activating Oxone to fully eliminate SUA in 30 min with a rate constant of 0.142 min(-1). CONCF exhibits a much lower Ea value of SUA degradation (35.2 kJ/mol) than reported values, and stable catalytic activities over multi-cyclic degradation of SUA. The mechanism of SUA degradation is also explored, and degradation intermediates of SUA degradation are identified to provide a possible pathway of SUA degradation. These features validate that CONCF is certainly a promising 3D hierarchical catalyst for enhanced Oxone activation to degrade SUA. The findings obtained here are also insightful to develop efficient heterogeneous Oxone-activating catalysts for eliminating emerging contaminants. (C) 2020 Elsevier Inc. All rights reserved.
机译:磺基水杨酸(SUA)作为一种医药产品被广泛使用,由于其低生物降解性,将其排放到环境中成为一个新兴的环境问题。因此,由于SO4-中心点-的许多优点,SO4-中心点-基高级氧化工艺已被提出用于降解SUA。由于氧酮是产生SO4中心点的主要试剂,而Co是激活氧酮以产生SO4中心点的最有能力的金属,因此开发一种有效但易于使用的用于氧酮活化以降解SUA的Co基催化剂至关重要。在本文中,通过将Co3O4纳米立方体(NCs)装饰在宏观掺氮碳形态(NCF)上,特别创建了一种3D分层催化剂。这种Co3O4装饰的NCF(CONCF)是独立的,宏观的,甚至可以挤压,以展示有趣和多功能的功能。更重要的是,CONCF由均匀分布在NCF上的Co3O4 NCs组成,无需聚集。NCF不仅可以作为Co3O4 NCs的载体,还可以提供额外的活性位点,协同增强对氧酮活化的催化活性。因此,与传统的Co3O4纳米颗粒相比,CONCF具有更高的催化活性,可以在30分钟内激活氧酮以完全消除SUA,速率常数为0.142分钟(-1)。CONCF对SUA降解的Ea值(35.2kj/mol)远低于文献报道的值,对SUA的多环降解具有稳定的催化活性。还探讨了SUA的降解机理,并确定了SUA降解的中间产物,为SUA的降解提供了可能的途径。这些特征验证了CONCF无疑是一种很有前途的3D分层催化剂,用于增强氧酮活化以降解SUA。本文的研究结果对于开发高效的多相氧酮活化催化剂以消除新出现的污染物也很有启发性。(C) 2020爱思唯尔公司版权所有。

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