Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
Uranyl-modified TiO 2 for complete photocatalytic oxidation of volatile organic compounds under UV and visible light. / Selishchev, Dmitry S.; Filippov, Tihon N.; Lyulyukin, Mikhail N. и др.
в: Chemical Engineering Journal, Том 370, 15.08.2019, стр. 1440-1449.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
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TY - JOUR
T1 - Uranyl-modified TiO 2 for complete photocatalytic oxidation of volatile organic compounds under UV and visible light
AU - Selishchev, Dmitry S.
AU - Filippov, Tihon N.
AU - Lyulyukin, Mikhail N.
AU - Kozlov, Denis V.
N1 - Funding Information: This work was supported by Ministry of Science and Higher Education of the Russian Federation (project АААА-А17-117041710087-3 ). Publisher Copyright: © 2019 Elsevier B.V.
PY - 2019/8/15
Y1 - 2019/8/15
N2 - Three commercially available TiO 2 powder photocatalysts and additional one synthesized in laboratory via the modification of anatase TiO 2 with uranyl nitrate (5 wt%) have been studied in the complete oxidation of several VOCs under UV (367 nm) and visible (450 nm) light. The kinetic curves for VOC removal, intermediate formation, and final product accumulation are presented in the paper and discussed in detail. The TiO 2 modification with uranyl ions (UO 2 2+ ) provides the ability for photocatalyst to absorb visible light with wavelength up to 500 nm. The photocatalytic activity of the uranyl-modified TiO 2 under visible light was up to 56 times higher than the activity of one of the best visible light sensitive commercial photocatalysts, KRONOClean® 7000 from Kronos Worldwide Inc. The complete oxidation of all the tested pollutants occurred over UO 2 2+ /TiO 2 both under UV and visible light. The formation of gaseous intermediates was observed for certain types of VOC, but the intermediates were further completely oxidized to carbon oxides and water under long-term irradiation. The kinetic regularities of PCO process under visible light were similar to the process under UV except somewhat prolonged kinetics due to lower photonic efficiency of light utilization in the visible spectral range.
AB - Three commercially available TiO 2 powder photocatalysts and additional one synthesized in laboratory via the modification of anatase TiO 2 with uranyl nitrate (5 wt%) have been studied in the complete oxidation of several VOCs under UV (367 nm) and visible (450 nm) light. The kinetic curves for VOC removal, intermediate formation, and final product accumulation are presented in the paper and discussed in detail. The TiO 2 modification with uranyl ions (UO 2 2+ ) provides the ability for photocatalyst to absorb visible light with wavelength up to 500 nm. The photocatalytic activity of the uranyl-modified TiO 2 under visible light was up to 56 times higher than the activity of one of the best visible light sensitive commercial photocatalysts, KRONOClean® 7000 from Kronos Worldwide Inc. The complete oxidation of all the tested pollutants occurred over UO 2 2+ /TiO 2 both under UV and visible light. The formation of gaseous intermediates was observed for certain types of VOC, but the intermediates were further completely oxidized to carbon oxides and water under long-term irradiation. The kinetic regularities of PCO process under visible light were similar to the process under UV except somewhat prolonged kinetics due to lower photonic efficiency of light utilization in the visible spectral range.
KW - TiO photocatalysis
KW - Uranyl ion (UO )
KW - UV
KW - Visible light
KW - VOC oxidation
KW - EXCITED-STATE
KW - FT-IR
KW - ION
KW - MODIFIED TITANIA
KW - AQUEOUS-SOLUTION
KW - TiO2 photocatalysis
KW - ANCHORED MCM-41
KW - DEGRADATION
KW - PHOTOCHEMISTRY
KW - MODIFIED OXIDES
KW - Uranyl ion (UO22+)
KW - PHOTOOXIDATION
UR - http://www.scopus.com/inward/record.url?scp=85063934102&partnerID=8YFLogxK
U2 - 10.1016/j.cej.2019.03.280
DO - 10.1016/j.cej.2019.03.280
M3 - Article
AN - SCOPUS:85063934102
VL - 370
SP - 1440
EP - 1449
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
SN - 1385-8947
ER -
ID: 19342016