Sciact
  • EN
  • RU

Mechanism of CH4 Dry Reforming on Nanocrystalline Doped Ceria-Zirconia with Supported Pt, Ru, Ni, and Ni–Ru Научная публикация

Конференция IX International Conference “Mechanisms of Catalytic Reactions”
22-25 окт. 2012 , Санкт-Петербург
Журнал Topics in Catalysis
ISSN: 1022-5528 , E-ISSN: 1572-9028
Вых. Данные Год: 2013, Том: 56, Номер: 11, Страницы: 958-968 Страниц : 11 DOI: 10.1007/s11244-013-0060-z
Ключевые слова Dry reforming, Me-supported doped ceria-zirconia, Mechanism, Methane, Oxygen bonding strength and reactivity, Transient kinetic studies
Авторы Bobin A.S. 1 , Sadykov V.A. 1,2 , Rogov V.A. 1,2 , Mezentseva N.V. 1,2 , Alikina G.M. 1 , Sadovskaya E.M. 1 , Glazneva T.S. 1 , Sazonova N.N. 1 , Smirnova M.Y. 1 , Veniaminov S.A. 1 , Mirodatos C. 3 , Galvita V. 4 , Marin G.B. 4
Организации
1 Boreskov Institute of Catalysis SB RAS, Prospect Akademika Lavrentieva, 5, 630090 Novosibirsk, Russia
2 Novosibirsk State University, Novosibirsk, Russia
3 Institut de Recherches sur la Catalyse et l’Environnement de Lyon, Lyon, France
4 University of Gent, Ghent, Belgium

Реферат: Specificity of CH4 dry reforming mechanism for Me-supported doped ceria-zirconia catalysts with high oxygen mobility was elucidated using a combination of transient kinetic methods (TAP, SSITKA) with pulse microcalorimetry and in situ FTIRS. Steady-state reaction of CH4 dry reforming is described by a simple redox scheme with independent stages of CH4 and CO2 activation. This is provided by easy CO2 dissociation on reduced sites of oxide supports followed by a fast oxygen transfer along the surface/domain boundaries to metal sites where CH4 molecules are transformed to CO and H2. The rate-limiting stage is irreversible transformation of CH4 on metal sites, while CO2 transformation proceeds much faster being reversible for steady-state surface. The oxygen forms responsible for CH4 selective transformation into syngas correspond to strongly bound bridging oxygen species with heats of desorption ≈600–650 kJ/mol O2, most probably bound with pairs of Pr and/or Ce cations able to change their oxidation state. Ni + Ru clusters could be involved in CO2 activation via facilitating C–O bond breaking in the transition state, thus increasing the rate constant of the surface reoxidation by CO2. Strongly bound carbonates are spectators.
Библиографическая ссылка: Bobin A.S. , Sadykov V.A. , Rogov V.A. , Mezentseva N.V. , Alikina G.M. , Sadovskaya E.M. , Glazneva T.S. , Sazonova N.N. , Smirnova M.Y. , Veniaminov S.A. , Mirodatos C. , Galvita V. , Marin G.B.
Mechanism of CH4 Dry Reforming on Nanocrystalline Doped Ceria-Zirconia with Supported Pt, Ru, Ni, and Ni–Ru
Topics in Catalysis. 2013. V.56. N11. P.958-968. DOI: 10.1007/s11244-013-0060-z WOS Scopus РИНЦ CAPlusCA OpenAlex
Даты:
Опубликована online: 10 мая 2013 г.
Опубликована в печати: 1 авг. 2013 г.
Идентификаторы БД:
Web of science: WOS:000321664200013
Scopus: 2-s2.0-84880410791
РИНЦ: 20442087
Chemical Abstracts: 2013:732372
Chemical Abstracts (print): 159:136789
OpenAlex: W2028527327
Цитирование в БД:
БД Цитирований
Web of science 65
Scopus 72
РИНЦ 69
OpenAlex 68
Альметрики: