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Degradation and mineralization of antipyrine by UV-A LED photo-Fenton reaction intensified by ferrioxalate with addition of persulfate

机译:通过加入过硫酸盐加入UV-A LED光芬顿反应的uV-A LED光芬顿反应的降解和矿化

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The intensification of the degradation of antipyrine in aqueous solution by using a UV-A-LED-photo-Fenton reaction intensified by ferrioxalate complexes and with addition of persulfate anions was studied. The efficiency of the reaction was evaluated in terms of antipyrine degradation and mineralization degree at different initial concentrations of hydrogen peroxide, ferrous ion, oxalic acid and persulfate anion. The reaction was carried out using a lab-scale photoreactor irradiated with artificial UV-A-LED light emitting at 365 nm. Artificial neural networks (NNs) were implemented for modelling the degradation process. Under optimal conditions, complete degradation of antipyrine and 93% mineralization was reached in 2.5 and 60 min, respectively. The contribution of Ha radicals in this system was evaluated running the reaction in the absence and presence of appropriate quenchers such as tert-butyl alcohol and methanol. In the last step of reaction, possibly different intermediates such as 2-butenedioic acid, butanedioic acid, 4-oxo-pentanoic acid, acetate and formate can be generated which cannot be degraded by Ha radicals or their reaction is very slow. This ferrioxalate-mediated system reduces the amount of H2O2 needed (100 mg L-1) for antipyrine degradation and persulfate was not necessary because it could not be activated with UV-A LED nor with Fe2+ since it is quickly converted to Fe3+ forming ferrioxalate complexes. (C) 2016 Elsevier B.V. All rights reserved.
机译:通过使用叔丙酸盐酸盐复合物加强的UV-A-LED光芬顿反应并加入过硫酸盐阴离子,加强水溶液中的反紫红液降解。在不同初始浓度的过氧化氢,亚铁离子,草酸和过硫酸盐阴离子的不同初始浓度下的反丝氨酸降解和矿化度方面评价反应的效率。使用用365nm发射的人造UV-A-LED发光照射的实验室级光反应器进行反应。实施人工神经网络(NNS),用于建模劣化过程。在最佳条件下,分别在2.5和60分钟内达到了对抗丝氨酸和93%矿化的完全降解。评估HA激进在该系统中的贡献在不存在和存在的情况下运行反应,例如叔丁醇和甲醇。在反应的最后一步中,可以产生可能不同的中间体,例如2-丁二酸,丁二酸,4-氧代戊酸,乙酸盐和甲酸盐,其不能通过HA自由基降解或它们的反应非常慢。该锰酸盐介导的系统减少了对抗丝氨酸降解所需的H2O2的量(100mg L-1),不需要过硫酸盐,因为它不能用UV-A LED和Fe2 +激活,因为它快速转化为Fe3 +形成叔丙酯络合物。 (c)2016年Elsevier B.v.保留所有权利。

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