Causes of Activation and Deactivation of Modified Nanogold Catalysts during Prolonged Storage and Redox Treatments; Molecules; Vol. 21, iss. 4

Bibliographic Details
Parent link:Molecules
Vol. 21, iss. 4.— 2016.— [486, 13 p.]
Corporate Author: Национальный исследовательский Томский политехнический университет Институт природных ресурсов Кафедра физической и аналитической химии
Other Authors: Kolobova E. N. Ekaterina Nikolaevna, Kotolevich Yu. I. Yuliya I., Pakrieva E. G. Ekaterina Germanovna, Mamontov G. V. Grigory Vladimirovich, Farias M. H. Mario H., Bogdanchikova N. E. Nina Evgenjevna, Cortes C. V. Corberan V., Pestryakov A. N. Aleksey Nikolaevich
Summary:The catalytic properties of modified Au/TiO2 catalysts for low-temperature CO oxidation are affected by deactivation and reactivation after long-term storage and by redox treatments. The effect of these phenomena on the catalysts was studied by HRTEM, BET, SEM, FTIR CO, XPS and H2 TPR methods. The main cause for the deactivation and reactivation of catalytic properties is the variation in the electronic state of the supported gold, mainly, the proportion of singly charged ions Au+. The most active samples are those with the highest proportion of singly charged gold ions, while catalysts with a high content of trivalent gold ions are inactive at low-temperatures. Active states of gold, resistant to changes caused by the reaction process and storage conditions, can be stabilized by modification of the titanium oxide support with transition metals oxides. The catalyst modified with lanthanum oxide shows the highest stability and activity.
Language:English
Published: 2016
Subjects:
Online Access:http://dx.doi.org/10.3390/molecules21040486
Format: Electronic Book Chapter
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=649093

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200 1 |a Causes of Activation and Deactivation of Modified Nanogold Catalysts during Prolonged Storage and Redox Treatments  |f E. N. Kolobova [et al.] 
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330 |a The catalytic properties of modified Au/TiO2 catalysts for low-temperature CO oxidation are affected by deactivation and reactivation after long-term storage and by redox treatments. The effect of these phenomena on the catalysts was studied by HRTEM, BET, SEM, FTIR CO, XPS and H2 TPR methods. The main cause for the deactivation and reactivation of catalytic properties is the variation in the electronic state of the supported gold, mainly, the proportion of singly charged ions Au+. The most active samples are those with the highest proportion of singly charged gold ions, while catalysts with a high content of trivalent gold ions are inactive at low-temperatures. Active states of gold, resistant to changes caused by the reaction process and storage conditions, can be stabilized by modification of the titanium oxide support with transition metals oxides. The catalyst modified with lanthanum oxide shows the highest stability and activity. 
461 |t Molecules 
463 |t Vol. 21, iss. 4  |v [486, 13 p.]  |d 2016 
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