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Degradation mechanism, reaction pathways and kinetics for the mineralization of Bisphenol A using hybrid ZnO/graphene oxide nano-catalysts

机译:使用杂交ZnO /石墨烯纳米催化剂的双酚A矿化的降解机理,反应途径和动力学

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摘要

Removal of Bisphenol A (BPA) from surface waters is necessary before consumption. A study, therefore, was conducted to degrade BPA using graphene oxide, ZnO and ZnO decorated on graphene oxide. Hydrothermal method was used to synthesize the hybrid nano-catalysts. 99.5% photocatalytic degradation of BPA was achieved by using ZG(0.6) nano-catalyst in comparison to bare ZnO and GO nano-catalysts at natural pH of 7.5 in 60 min of UV irradiation. The higher photocatalytic activity of ZG(0.6) nano-catalyst could be ascribed to an improved surface area, efficient charge separation as well as the decreased recombination rate of electron-hole charge carriers, leading to the generation of highly reactive hydroxyl radicals for the degradation of BPA. Photocatalytic degradation followed Langmuir-Hinshelwood model with pseudo-first-order kinetics. The degradation mechanism is also detailed with identification of reaction intermediates. Degradation pathways, based on LCMS analysis, have been proposed. The pathways revealed the formation of smaller by-products such as phenol, hydroquinol and (Z)-3-hydroxyacrylaldehyde. The developed ZG(0.6) nano-catalyst were found to be reusable for consecutive five runs without much loss in the activity and have the advantage of effective charge separation.
机译:在消耗之前,需要从表面水中除去双酚A(BPA)。因此,研究了使用石墨烯氧化物,ZnO和ZnO在石墨烯氧化物上进行降解BPA。水热法用于合成杂化纳米催化剂。通过使用Zg(0.6)纳米催化剂与裸ZnO相比,实现了BPA的99.5%光催化降解BPA,并在60分钟的UV辐射中在7.5的天然pH下进行纳米催化剂。 Zg(0.6)纳米催化剂的较高的光催化活性可以归因于改进的表面积,有效的电荷分离以及电子空穴电荷载体的重组率降低,导致用于降解的高反应性羟基的产生BPA。光催化退化遵循琅勃马 - 欣斯伍德模型,具有伪一阶动力学。还通过鉴定反应中间体进行降解机制。已经提出了基于LCMS分析的降解途径。该途径揭示了较小的副产物,例如苯酚,羟基喹啉和(Z)-3-羟基丙烯醛。发现型Zg(0.6)纳米催化剂在连续五个运行中可重复使用,而在活性中没有太大损失,并且具有有效电荷分离的优点。

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