Green Oxidation of n-Octanol on Supported Nanogold Catalysts: Formation of Gold Active Sites under Combined Effect of Gold Content, Additive Nature and Redox Pretreatment

Bibliographic Details
Parent link:ChemCatChem
Vol. 11, iss. 6.— 2019.— [P. 1615-1624]
Corporate Author: Национальный исследовательский Томский политехнический университет (ТПУ) Институт природных ресурсов (ИПР) Кафедра технологии органических веществ и полимерных материалов (ТОВПМ)
Other Authors: Pakrieva E. G. Ekaterina Germanovna, Kolobova E. N. Ekaterina Nikolaevna, Mamontov G. Ya. Gennady Yakovlevich, Bogdanchikova N., Farias M. H. Mario, Pascual L., Cortes C. V. Corberan, Martinez G. S. Gonzalez, Carabineiro Sa. C., Pestryakov A. N. Aleksey Nikolaevich
Summary:Title screen
The combined influence of gold content (0.5 or 4?wt.?%), modifying additives (La or Ce oxides) and redox pretreatments (H2 or O2) on catalytic properties and formation of active sites of Au/TiO2 in the selective oxidation of n?octanol under mild conditions was studied. Samples were characterized by BET, XRD, EDX, ICP, TEM, STEM?HAADF, CO2?TPD, H2?TPR and XPS methods. The order of catalytic activity depended on the support nature for all treated samples, as follows: Au/La2O3/TiO2>Au/CeO2/TiO2>Au/TiO2. The catalytic activity enhanced with the increase of gold loading in the samples with hydrogen pretreatment, while after the oxidative pretreatment of the catalysts the opposite dependence of the activity with the gold content was found. This catalytic behavior was explained by a change in the surface concentration of monovalent gold ions, which seemed to be the active sites. The most active catalyst, 0.5?% Au/La2O3/TiO2, pretreated in oxidative atmosphere, had the highest surface concentration of monovalent gold ions.
Режим доступа: по договору с организацией-держателем ресурса
Language:English
Published: 2019
Subjects:
Online Access:https://doi.org/10.1002/cctc.201801566
Format: Electronic Book Chapter
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=659720