自然光照下磷酸盐基金属有机骨架光催化脱除双酚a的研究

A. Farrokhi, Farzaneh Bivareh, Saeideh Dejbakhshpour, A. Z. Moghaddam
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引用次数: 0

摘要

双酚A是水生环境中应用最广泛和新兴的污染物之一,本文研究了在自然光照下采用高级氧化法光催化去除双酚A。采用磷酸配体STA-12 (Fe)和过氧化氢合成的金属有机骨架去除效果良好。为此,研究了光- fenton降解双酚A的最佳条件。在过氧化氢/太阳光/STA-12 (Fe)的催化体系中观察到明显的协同作用,污染物的去除过程遵循一级动力学。在30 mg / l的水溶液中,双酚A氧化的最佳pH值为5 μl,最佳照射时间为90 min,最佳催化剂用量为10 mg,最佳H2O2用量为12 μl。在此条件下,最佳去除率为79.8%。通过测定TOC,确定有机污染物的矿化值为51%。为了确定影响光催化还原的最重要物种,利用各种清除剂进行了捕集实验,结果表明,羟基自由基(•OH)是光催化体系中的主要氧化剂,超氧自由基和光催化剂表面的孔较少参与污染物降解过程。最后,详细探讨了可能的反应机理。此外,该催化剂在光催化反应中具有可回收性和稳定性。本研究首次报道了磷酸盐基MOF在光- fenton机制下去除新兴污染物的应用,为太阳能驱动的高级氧化工艺在水源处理和环境保护方面提供了新的范例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Photocatalytic application of a phosphonate-based metal-organic framework for the removal of bisphenol A under natural sunlight
Photocatalytic removal of bisphenol A, one of the most widely and emerging pollutants in the aquatic environment, was investigated by advanced oxidation process under natural sunlight. The removal process by a metal-organic framework, synthesized with phosphonic acid ligand, namely STA-12 (Fe) and hydrogen peroxide revealed excellent results. Therefore, the optimal conditions for the degradation of bisphenol A by the photo-Fenton mechanism were studied. The removal process follows the first-order kinetics with respect to the contaminant and a significant synergy was observed in the catalytic system of hydrogen peroxide/sunlight/STA-12 (Fe). The Optimal values for pH, irradiation time, catalyst amount and H2O2 dosage for oxidation of bisphenol A in 30 mg / l aqueous solution were determined to be 5, 90 minutes, 10 mg and 12 μl, respectively. Under these conditions, the best removal efficiency was 79.8%. Also, the mineralization value of organic pollutant was determined to equal 51% by measuring TOC. To determine the most important species that affected the photocatalytic reduction, trapping experiments were carried out, using various kinds of scavengers and the results showed that the hydroxyl radicals (•OH) are the main oxidizing agent in the photocatalytic system and superoxide radical and the holes in the photocatalyst surface are less involved in the process of contaminant degradation. Finally, a probable reaction mechanism has been investigated in detail. In addition, the catalyst has recyclability and stability in the photocatalytic reaction. This study is the first report for application of a phosphonate-based MOF for the removal of an emerging pollutant with a photo-Fenton mechanism and presents a new example of solar-driven advanced oxidation process for the treatment of aquatic sources and environmental protection.
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