Basic Sites on the Oxide Surfaces: Their Effect on the Catalytic Methane Coupling
Научная публикация
| Общее |
Язык:
Английский,
Жанр:
Статья (Full article),
Статус опубликования:
Опубликована,
Оригинальность:
Оригинальная
|
| Конференция |
2nd Workshop on C1-C3 Hydrocarbon Conversion
27-30 июн. 1994
,
Krasnoyarsk
|
| Журнал |
Catalysis Today
ISSN: 0920-5861
, E-ISSN: 1873-4308
|
| Вых. Данные |
Год: 1995,
Том: 24,
Номер: 3,
Страницы: 225-230
Страниц
: 6
DOI:
10.1016/0920-5861(95)00029-F
|
| Ключевые слова |
PROMOTED MAGNESIUM-OXIDE; OXIDATIVE DIMERIZATION; SPECTROSCOPY |
| Авторы |
Davydov A.A.
1
,
Shepotko M.L.
2
,
Budneva A.A.
1
|
| Организации |
| 1 |
Boreskov Institute of Catalysis, Novosibirsk, Russia
|
| 2 |
Institute of Solid State Chemistry, Novosibirsk, Russia
|
|
Basic sites of various oxide catalysts for oxidative methane coupling have been studied with the IR spectra of CO2 probe molecules. It is possible to determine the concentration and strength of surface basic sites, by studying carbonate compounds, which form on surface oxygen sites. Since the surface structure is non-uniform, its oxygen ions carry different negative effective charges and thus produce carbonates, exhibiting different IR spectra. A correlation between the site strengths and carbonates' spectral behavior, found earlier, allows us to distinguish the sites rather well. The catalytic activity of oxide catalysts was found to depend on the presence and concentration of the strongest basic sites on the oxide surface.