Supported Gold Nanoparticles as Catalysts in Peroxidative and Aerobic Oxidation of 1-Phenylethanol under Mild Conditions

書誌詳細
Parent link:Nanomaterials
Vol. 10, iss. 151.— 2020
その他の著者: Pakrieva E. G. Ekaterina Germanovna, Ribeiro A., Kolobova E. N. Ekaterina Nikolaevna, Martins L., Carabineiro S. A. C. Sonia Alexandra Correia, German D. Y. Dmitry Yurjevich, Pichugina D. Darjya, Jiang C. Ce, Bogdanchikova N. Nina, Corberan V. C., Pestryakov A. N. Aleksey Nikolaevich
要約:Title screen
The efficiency of Au/TiO₂ based catalysts in 1-phenylethanol oxidation was investigated. The role of support modifiers (La₂O₃ or CeO₂), influence of gold loading (0.5% or 4%) and redox pretreatment atmosphere, catalyst recyclability, effect of oxidant: tert-butyl hydroperoxide (TBHP) or O₂, as well as the optimization of experimental parameters of the reaction conditions in the oxidation of this alcohol were studied and compared with previous studies on 1-octanol oxidation. Samples were characterized by temperature-programmed oxygen desorption (O₂-TPD) method. X-ray photoelectron spectroscopy (XPS) measurements were carried out for used catalysts to find out the reason for deactivation in 1-phenylethanol oxidation. The best catalytic characteristics were shown by catalysts modified with La₂O₃, regardless of the alcohol and the type of oxidant. When O₂ was used, the catalysts with 0.5% Au, after oxidative pretreatment, showed the highest activity in both reactions. The most active catalysts in 1-phenylethanol oxidation with TBHP were those with 4% Au and the H₂ treatment, while under the same reaction conditions, 0.5% Au and O2 treatment were beneficial in 1-octanol oxidation. Despite the different chemical nature of the substrates, it seems likely that Au⁺(Auⁿ⁺) act as the active sites in both oxidative reactions. Density functional theory (DFT) simulations confirmed that the gold cationic sites play an essential role in 1-phenylethanol adsorption.
言語:英語
出版事項: 2020
主題:
オンライン・アクセス:http://dx.doi.org/10.3390/nano10010151
フォーマット: 電子媒体 図書の章
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=663632