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Fe@柚子皮衍生生物炭复合材料对邻硝基苯酚的高效降解及其同时还原氧化过程的机理。

Efficient degradation of p-nitrophenol by Fe@pomelo peel-derived biochar composites and its mechanism of simultaneous reduction and oxidation process.

机构信息

Tianjin Engineering Center of Environmental Diagnosis and Contamination Remediation, Tianjin, 300350, China; MOE Key Laboratory of Pollution Processes and Environmental Criteria, College of Environmental Science and Engineering, Nankai University, Tianjin, 300350, China.

Tianjin Engineering Center of Environmental Diagnosis and Contamination Remediation, Tianjin, 300350, China; MOE Key Laboratory of Pollution Processes and Environmental Criteria, College of Environmental Science and Engineering, Nankai University, Tianjin, 300350, China.

出版信息

Chemosphere. 2021 Mar;267:129213. doi: 10.1016/j.chemosphere.2020.129213. Epub 2020 Dec 8.

Abstract

In this study, waste pomelo peels (PP) mixed with iron salts was treated successively with hydrothermal and pyrolyzing carbonization processes to obtain Fe(0) containing biochar composites (Fe@PP-Hy-Py) and the catalytic degradation of p-nitrophenol (PNP) using these Fe@PP-Hy-Py composites was studied. The results showed that the hydrothermal pre-treatment of the mixture of iron salts and pomelo peels was favorable for the incorporation of iron precursor within biomass network, which enabled copolymerization during the following pyrolysis. Through the pyrolysis process, the iron precursor was reduced in situ to amorphous Fe(0) dopped into the carbonaceous matrix, which conversely decreased the defect and disorder degree of pseudo-graphitic carbons and catalyzed the formation of environmental persistent free radicals (EPFRs). Degradation tests showed that the composites obtained at 600 °C with the theoretical Fe mass loading of 10% exhibited the greatest PNP degradation efficiency. Over 90% of 10 mg/L PNP was removed in 2 min under both N and air conditions with 1.0 g/L of catalyst level. The degradation kinetics of PNP were all well fitted by the pseudo-first-order kinetics model with k of Fe@PP-Hy-Py being 0.953 min. HPLC-QTOF/MS analysis demonstrated that both oxidation and reduction of PNP occurred as indicated by the detection of 4-aminophenol and ring opening compounds. The Fe(0) on the Fe@PP-Hy-Py was responsible for the reduction of PNP, while oxidation was induced by EPFRs. This study highlights the feasibility of synthesizing active heterogeneous Fe(0)-biochar composites by hydrothermal-pyrolysis route and the associated mechanisms of pollutant degradation.

摘要

在这项研究中,将废柚子皮(PP)与铁盐混合,依次进行水热和热解碳化处理,得到负载 Fe(0) 的生物炭复合材料(Fe@PP-Hy-Py),并研究了这些 Fe@PP-Hy-Py 复合材料对 p-硝基苯酚(PNP)的催化降解作用。结果表明,铁盐和柚子皮混合物的水热预处理有利于铁前体在生物质网络内的掺入,从而在随后的热解过程中实现共聚。通过热解过程,铁前体原位还原为非晶态 Fe(0) 掺杂到碳质基质中,这反过来降低了类石墨碳的缺陷和无序程度,并催化了环境持久性自由基(EPFRs)的形成。降解实验表明,在 600°C 下获得的理论铁质量负载为 10%的复合材料在 N 和空气条件下具有最大的 PNP 降解效率。在 1.0 g/L 催化剂水平下,10 mg/L PNP 的去除率在 2 分钟内超过 90%。PNP 的降解动力学均很好地符合准一级动力学模型,Fe@PP-Hy-Py 的 k 值为 0.953 min。HPLC-QTOF/MS 分析表明,PNP 发生了氧化和还原反应,检测到了 4-氨基酚和开环化合物。Fe@PP-Hy-Py 上的 Fe(0) 负责还原 PNP,而氧化则由 EPFRs 引起。本研究强调了通过水热-热解途径合成活性异质 Fe(0)-生物炭复合材料的可行性及其相关污染物降解机制。

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