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Simultaneous adsorption and oxidative degradation of Bisphenol A by zero-valent iron/iron carbide nanoparticles encapsulated in N-doped carbon matrix

机译:氮掺杂碳基中包裹的零价铁/碳化铁纳米粒子同时吸附和氧化双酚A

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摘要

The increased release and accumulation of Bisphenol A (BPA) in contaminated wastewater has resulted in the world wide concerns because of its potential negative effects on human health and aquatic ecosystems. Starting with metal-organic frameworks, we present a simple method to synthesize magnetic porous microcubes (N-doped Fe-0/Fe3C@C) with graphitized shell and highly dispersed active kernel via the pyrolysis process under N-2 atmosphere. Batch adsorption experimental results showed that N-doped Fe-0/Fe3C@C had high adsorption capacity for SPA (similar to 138 mg g(-1) at pH = 7 and 298 K). Degradation of BPA adsorbed on N-doped Fe-0/Fe3C@C was further investigated as a function of BPA concentration, persulfate amount, temperature and solution pH. It was found that potassium peroxodisulfate could be activated by N-doped Fe-0/Fe3C@C, and a large number of free radicals were generated which was crucial for the degradation of BPA. The concentration of BPA was barely changed in the individual persulfate system. BPA (10 mg L-1) was almost completely degraded within 60 min in the presence of N-doped BPA (10 mg L-1) was almost completely degraded within 60 min in the presence of N-doped Fe-0/Fe3C@C (similar to 0.2 g L-1). When the BPA content increased to 25 mg L-1, the removal efficiency of BPA achieved to 98.4% after 150 min. From the XRD, Raman, and XPS analysis, the main adsorption mechanism of BPA was pi-pi interactions between the pi orbital on the carbon basal planes and the electronic density in the BPA aromatic rings. While the superior degradation was attributed to the radical generation and evolution in phenol oxidation. This work not only proved the potential application of N-doped Fe-0/Fe3C@C in the adsorption and degradation of BPA, but also opened the new possibilities to eliminate organic pollutants using this kind of magnetic materials in organic pollutants' cleanup. (C) 2018 Published by Elsevier Ltd.
机译:由于双酚A(BPA)对人体健康和水生生态系统的潜在负面影响,双酚A(BPA)在受污染的废水中的释放和积累增加,引起了全世界的关注。从金属有机框架开始,我们提出了一种简单的方法,通过在N-2气氛下的热解过程,合成具有石墨化壳和高度分散的活性核的磁性多孔微立方体(N掺杂的Fe-0 / Fe3C @ C)。批量吸附实验结果表明,氮掺杂的Fe-0 / Fe3C @ C对SPA具有很高的吸附能力(在pH = 7和298 K时类似于138 mg g(-1))。进一步研究了吸附在氮掺杂的Fe-0 / Fe3C @ C上的BPA的降解与BPA浓度,过硫酸盐量,温度和溶液pH的关系。发现过二硫酸钾可被氮掺杂的Fe-0 / Fe3C @ C活化,并产生大量自由基,这对BPA的降解至关重要。在单独的过硫酸盐体系中,BPA的浓度几乎没有变化。 BPA(10 mg L-1)在N掺杂存在下60分钟内几乎完全降解BPA(10 mg L-1)在N掺杂Fe-0 / Fe3C @存在下60分钟内几乎完全降解C(类似于0.2 g L-1)。当BPA含量增加到25 mg L-1时,BPA的去除效率在150分钟后达到98.4%。从XRD,拉曼和XPS分析来看,BPA的主要吸附机理是碳基面上的pi轨道与BPA芳环中的电子密度之间的pi-pi相互作用。而优异的降解归因于自由基的产生和酚氧化的演化。这项工作不仅证明了N掺杂的Fe-0 / Fe3C @ C在BPA的吸附和降解中的潜在应用,而且为使用这种磁性材料清除有机污染物中的有机污染物开辟了新的可能性。 (C)2018由Elsevier Ltd.发布

著录项

  • 来源
    《Environmental Pollution》 |2018年第ptaa期|218-227|共10页
  • 作者单位

    North China Elect Power Univ, Coll Environm Sci & Engn, Beijing 102206, Peoples R China;

    North China Elect Power Univ, Coll Environm Sci & Engn, Beijing 102206, Peoples R China;

    North China Elect Power Univ, Coll Environm Sci & Engn, Beijing 102206, Peoples R China;

    North China Elect Power Univ, Coll Environm Sci & Engn, Beijing 102206, Peoples R China;

    North China Elect Power Univ, Coll Environm Sci & Engn, Beijing 102206, Peoples R China;

    North China Elect Power Univ, Coll Environm Sci & Engn, Beijing 102206, Peoples R China;

    North China Elect Power Univ, Coll Environm Sci & Engn, Beijing 102206, Peoples R China;

    North China Elect Power Univ, Coll Environm Sci & Engn, Beijing 102206, Peoples R China;

    King Abdulaziz Univ, NAAM Res Grp, Fac Sci, Jeddah 21589, Saudi Arabia;

    North China Elect Power Univ, Coll Environm Sci & Engn, Beijing 102206, Peoples R China;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    N-doped Fe-0/Fe3C@C; Adsorption; Degradation; Bisphenol A; Radicals;

    机译:氮掺杂Fe-0 / Fe3C @ C;吸附;降解;双酚A;自由基;

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