TY - JOUR
T1 - Addition of SnO2 over an oxygen deficient zirconium oxide (ZrxOy) and its catalytic evaluation for the photodegradation of phenol in water
AU - Tzompantzi, Francisco
AU - Castillo-Rodríguez, J. C.
AU - Tzompantzi-Flores, C.
AU - Pérez-Hernández, Raúl
AU - Gómez, R.
AU - Santolalla-Vargas, C. E.
AU - Che-Galicia, Gamaliel
AU - Ramos-Ramírez, Esthela
N1 - Publisher Copyright:
© 2021 Elsevier B.V.
PY - 2022/7/1
Y1 - 2022/7/1
N2 - The ZrSn composites materials were prepared in one pot by chemical co-precipitation method. SnO2 was incorporated to ZrxOy modifying the molar percentage from 1 to 5 mol%. The ZrSn composites were characterized by different techniques: XRD, FTIR, DRS, SEM, N2 physisorption and HR-TEM. The ZrSn composites were dried at 80 °C and thereafter were evaluated in the photodegradation of phenol under UV irradiation. The percentages of degradation and mineralization were determined after a reaction time of 150 min by UV–Vis spectroscopy and Total Organic Carbon analysis (TOC), respectively. The composite containing SnO2 in a 3 mol% showed the highest photoactivity with a 72% of photodegradation, a higher value compared with the obtained with TiO2-P25 (62%). Finally, a possible reaction mechanism was proposed based on certain studies, which allows to follow the formation of the active species •OH, •O2− and h+. The formation of the •OH specie was measured by fluorescence spectroscopy whereas the inhibition of the species •O2− and h+ was determined by UV–Vis spectroscopy. The results showed that the ZrSn composites not promotes the hydroxyl radical formation. In addition, the holes capture showed a full-loss of the photoactivity while the minimization of (•O2−) radicals in the reaction media results in a decrement of the photoactivity. The formation of heterojunctions and the presence of localized states in the synthesized composites offer an excellent alternative for a fast photodegradation of phenol.
AB - The ZrSn composites materials were prepared in one pot by chemical co-precipitation method. SnO2 was incorporated to ZrxOy modifying the molar percentage from 1 to 5 mol%. The ZrSn composites were characterized by different techniques: XRD, FTIR, DRS, SEM, N2 physisorption and HR-TEM. The ZrSn composites were dried at 80 °C and thereafter were evaluated in the photodegradation of phenol under UV irradiation. The percentages of degradation and mineralization were determined after a reaction time of 150 min by UV–Vis spectroscopy and Total Organic Carbon analysis (TOC), respectively. The composite containing SnO2 in a 3 mol% showed the highest photoactivity with a 72% of photodegradation, a higher value compared with the obtained with TiO2-P25 (62%). Finally, a possible reaction mechanism was proposed based on certain studies, which allows to follow the formation of the active species •OH, •O2− and h+. The formation of the •OH specie was measured by fluorescence spectroscopy whereas the inhibition of the species •O2− and h+ was determined by UV–Vis spectroscopy. The results showed that the ZrSn composites not promotes the hydroxyl radical formation. In addition, the holes capture showed a full-loss of the photoactivity while the minimization of (•O2−) radicals in the reaction media results in a decrement of the photoactivity. The formation of heterojunctions and the presence of localized states in the synthesized composites offer an excellent alternative for a fast photodegradation of phenol.
KW - Phenol photodegradation
KW - ZrSn composites
UR - http://www.scopus.com/inward/record.url?scp=85112511157&partnerID=8YFLogxK
U2 - 10.1016/j.cattod.2021.07.027
DO - 10.1016/j.cattod.2021.07.027
M3 - Artículo
AN - SCOPUS:85112511157
SN - 0920-5861
VL - 394-396
SP - 376
EP - 389
JO - Catalysis Today
JF - Catalysis Today
ER -