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Solar photocatalytic decomposition of ethyl paraben in zinc oxide suspensions

Frontistis Zacharias, Antonopoulou Maria, Venieri Danai, Dailianis Stefanos, Konstantinou, Ioannis K, Mantzavinos, Dionissios

Πλήρης Εγγραφή


URI: http://purl.tuc.gr/dl/dias/5E3BA269-5937-4C71-AA22-977D0DB04BF7
Έτος 2017
Τύπος Δημοσίευση σε Περιοδικό με Κριτές
Άδεια Χρήσης
Λεπτομέρειες
Βιβλιογραφική Αναφορά Z. Frontistis, M. Antonopoulou, D. Venieri, S. Dailianis, I. Konstantinou and D. Mantzavinos, "Solar photocatalytic decomposition of ethyl paraben in zinc oxide suspensions," Catal. Today, vol. 280, pt. 1, pp. 139-148, Feb. 2017. doi: 10.1016/j.cattod.2016.06.008 https://doi.org/10.1016/j.cattod.2016.06.008
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Περίληψη

The photocatalytic degradation of ethyl paraben (EP) in zinc oxide (ZnO) suspensions under simulated solar radiation was investigated. The effect of EP concentration (500–1500 μg/L), ZnO concentration (100–500 mg/L), reaction time (3–9 min), initial pH (3–9), light intensity (7.3 10−7–1.1 10−6 einstein/(L.s)) and the water matrix (0–10 mg/L of humic acid) on degradation was evaluated implementing a factorial design methodology. Of the six variables tested, EP concentration, ZnO concentration, reaction time and the water matrix were found to be statistically significant variables, and also important was the second order interaction of EP concentration with reaction time. With the exception of the water matrix, all other effects were positive with respect to the concentration of EP removed. Experiments at increased EP concentration (20 mg/L) were performed to identify transformation products (TPs) and assess the extent of mineralization. LC-TOF-MS analysis revealed the formation of seven early-stage TPs through hydroxylation and dealkylation reactions and a plausible reaction pathway was proposed. Besides the identified TPs, other unidentified TPs were also formed as has been verified measuring the extent of mineralization and performing a carbon balance in the liquid phase. EP at 20 mg/L exhibited mild estrogenic activity, which was partially removed upon oxidation. The stability of ZnO was evaluated measuring the extent of zinc leaching, which was just 1.5%; moreover, ZnO was found to be more active than reference P25 TiO2 for EP degradation and mineralization.

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