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天然凹凸棒石衍生的铁锰尖晶石氧化物作为过硫酸盐活化降解四环素的多相催化剂的开发。

Development of natural attapulgite derived ferromanganese spinel oxides as heterogeneous catalysts for persulfate activation of tetracycline degradation.

作者信息

Hu Zhenzhong, Tang Xuejing, Ma Xiaojia, Guo Sheng-Qi, Zhen Mengmeng, Ning Jingxia, Xu Sheng, Shen Boxiong

机构信息

Hebei Engineering Research Center of Pollution Control in Power System, Tianjin 300401, China; Tianjin Key Laboratory of Clean Energy and Pollutant Control, Tianjin 300401, China; School of Energy and Environmental Engineering, Hebei University of Technology, China.

Hebei Engineering Research Center of Pollution Control in Power System, Tianjin 300401, China; Tianjin Key Laboratory of Clean Energy and Pollutant Control, Tianjin 300401, China; School of Energy and Environmental Engineering, Hebei University of Technology, China.

出版信息

Chemosphere. 2024 Mar;352:141428. doi: 10.1016/j.chemosphere.2024.141428. Epub 2024 Feb 9.

Abstract

Ferromanganese spinel oxides (MnFeO, MFO) have been proven effective in activating persulfate for pollutants removal. However, their inherent high surface energy often leads to agglomeration, diminishing active sites and consequently restricting catalytic performance. In this study, using Al-MCM-41 (MCM) mesoporous molecular sieves derived from natural attapulgite as a support, the MFO/MCM composite was synthesized through dispersing MnFeO nanoparticles on MCM carrier by a simple hydrothermal method, which can effectively activate persulfate (PS) to degrade Tetracycline (TC). The addition of Al-MCM-41 can effectively improve the specific surface area and adsorption performance of MnFeO, but also reduce the leaching amount of metal ions. The MFO/MCM composite exhibited superior catalytic reactivity towards PS and 84.3% removal efficiency and 64.7% mineralization efficiency of TC (20 mg/L) was achieved in 90 min under optimized conditions of 0.05 mg/L catalyst dosage, 5 mM PS concentration, room temperature and no adjustment of initial pH. The effects of various stoichiometric MFO/MCM ratio, catalyst dosage, PS concentration, initial pH value and co-existing ions on the catalytic performance were investigated in detail. Moreover, the possible reaction mechanism in MFO-MCM/PS system was proposed based on the results of quenching tests, electron paramagnetic resonance (EPR) and XPS analyses. Finally, major degradation intermediates of TC were detected by liquid chromatography mass spectrometry technologies (LC-MS) and four possible degradation pathways were proposed. This study enhances the design approach for developing highly efficient, environmentally friendly and low-cost catalysts for the advanced treatment process of antibiotic wastewater.

摘要

铁锰尖晶石氧化物(MnFeO,MFO)已被证明在活化过硫酸盐以去除污染物方面是有效的。然而,它们固有的高表面能常常导致团聚,减少活性位点,从而限制催化性能。在本研究中,以天然凹凸棒石衍生的Al-MCM-41(MCM)介孔分子筛为载体,通过简单的水热法将MnFeO纳米颗粒分散在MCM载体上合成了MFO/MCM复合材料,该复合材料能有效活化过硫酸盐(PS)以降解四环素(TC)。Al-MCM-41的加入不仅能有效提高MnFeO的比表面积和吸附性能,还能降低金属离子的浸出量。MFO/MCM复合材料对PS表现出优异的催化活性,在0.05 mg/L催化剂用量、5 mM PS浓度、室温且不调节初始pH的优化条件下,90分钟内实现了20 mg/L TC的84.3%去除效率和64.7%矿化效率。详细研究了不同化学计量比的MFO/MCM、催化剂用量、PS浓度、初始pH值和共存离子对催化性能的影响。此外,基于猝灭试验、电子顺磁共振(EPR)和XPS分析结果,提出了MFO-MCM/PS体系中可能的反应机理。最后,通过液相色谱质谱技术(LC-MS)检测了TC的主要降解中间体,并提出了四种可能的降解途径。本研究为开发用于抗生素废水深度处理的高效、环保和低成本催化剂提供了设计方法。

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