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污水污泥衍生多孔碳对萘染料中间体的吸附和类 Fenton 降解。

Adsorption and Fenton-like degradation of naphthalene dye intermediate on sewage sludge derived porous carbon.

机构信息

School of Environmental Science and Engineering, Shanghai Jiao Tong University, Shanghai 200240, China.

出版信息

J Hazard Mater. 2013 Feb 15;246-247:145-53. doi: 10.1016/j.jhazmat.2012.12.012. Epub 2012 Dec 16.

Abstract

A sewage sludge derived porous carbon (SC), which was prepared by physicochemical activation and carbonization (600°C), was applied for the adsorption and degradation of 1-diazo-2-naphthol-4-sulfonic acid (1,2,4-Acid) in the presence of H(2)O(2) and the performance was compared to that of pure Fe(3)O(4) magnetic nanoparticles (MNPs). The prepared SC showed mesoporous structure with magnetic property, which made it favorable for solid-liquid separation application. Further experiments revealed that SC had a higher adsorption capacity and degradation efficiency of 1,2,4-Acid than bare Fe(3)O(4). The Langmuir and Freundlich model fitted the isotherm data and illustrated that the equilibrium adsorption amount of 1,2,4-Acid onto SC (95.1 mg g(-1)) was quadruple as large as that on Fe(3)O(4) (26.4 mg g(-1)). The subsequent degradation experiments were conducted at conditions (pH 5.0 in the presence of 15 mM H(2)O(2)) with regard to 1,2,4-Acid degradation efficiency and metal ions leach. The 120 min's treatment in SC/H(2)O(2) system achieved 94% of 1,2,4-Acid (from 150 mg L(-1) after adsorption equilibrium to 9 mg L(-1)) and 48.1% TOC reduction, far higher than the efficiency of 46% and 24.3% by using Fe(3)O(4) MNPs. Further analysis evidenced the co-catalytic effect of iron, carbon, silicon and aluminum, which existed in large quantities in sludge derived SC. The carbonaceous phase along with silica contributes to an increase in the dispersion of catalytic centers and an adsorbent to concentrate organic pollutant whereas the iron oxide as well as alumina provides the catalytic centers for a Haber-Weiss initiated reactions.

摘要

一种由物理化学活化和碳化(600°C)制备的污水污泥衍生多孔碳(SC),用于在 H(2)O(2)存在下吸附和降解 1-重氮-2-萘酚-4-磺酸(1,2,4-酸),并将其性能与纯 Fe(3)O(4)磁性纳米颗粒(MNPs)进行了比较。所制备的 SC 具有介孔结构和磁性,有利于固液分离应用。进一步的实验表明,SC 对 1,2,4-酸的吸附容量和降解效率均高于裸 Fe(3)O(4)。Langmuir 和 Freundlich 模型拟合了等温线数据,并说明 1,2,4-酸在 SC(95.1mg g(-1))上的平衡吸附量是在 Fe(3)O(4)(26.4mg g(-1))上的四倍。随后在考虑 1,2,4-酸降解效率和金属离子浸出的条件下(pH 5.0 存在 15mM H(2)O(2))进行了后续降解实验。在 SC/H(2)O(2)系统中处理 120 分钟可实现 94%的 1,2,4-酸(从吸附平衡时的 150mg L(-1)降至 9mg L(-1))和 48.1%TOC 减少,远高于使用 Fe(3)O(4)MNPs 达到的 46%和 24.3%的效率。进一步的分析证明了存在于大量污泥衍生的 SC 中的铁、碳、硅和铝的共催化作用。含碳相和硅有助于增加催化中心的分散和吸附剂浓缩有机污染物,而氧化铁和氧化铝则为 Haber-Weiss 引发的反应提供催化中心。

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