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Enhanced Sulfur Tolerance of Ceria-Promoted NOx Storage Reduction (NSR) Catalysts: Sulfur Uptake, Thermal Regeneration and Reduction with H2(g) Научная публикация

Журнал Topics in Catalysis
ISSN: 1022-5528 , E-ISSN: 1572-9028
Вых. Данные Год: 2013, Том: 56, Номер: 11, Страницы: 950-957 Страниц : 8 DOI: 10.1007/s11244-013-0059-5
Авторы Say Zafer 1 , Vovk Evgeny I. 2 , Bukhtiyarov Valerii I. 2 , Ozensoy Emrah 1
Организации
1 Department of Chemistry, Bilkent University, Ankara, Turkey
2 Boreskov Institute of Catalysis, Novosibirsk, Russia
Реферат: SO x uptake, thermal regeneration and the reduction of SO x via H2(g) over ceria-promoted NSR catalysts were investigated. Sulfur poisoning and desulfation pathways of the complex BaO/Pt/CeO2/Al2O3 NSR system was investigated using a systematic approach where the functional sub-components such as Al2O3, CeO2/Al2O3, BaO/Al2O3, BaO/CeO2/Al2O3, and BaO/Pt/Al2O3 were studied in a comparative fashion. Incorporation of ceria significantly increases the S-uptake of Al2O3 and BaO/Al2O3 under both moderate and extreme S-poisoning conditions. Under moderate S-poisoning conditions, Pt sites seem to be the critical species for SO x oxidation and SO x storage, where BaO/Pt/Al2O3 and BaO/Pt/CeO2/Al2O3 catalysts reveal a comparable extent of sulfation. After extreme S-poisoning due to the deactivation of most of the Pt sites, ceria domains are the main SO x storage sites on the BaO/Pt/CeO2/Al2O3 surface. Thus, under these conditions, BaO/Pt/CeO2/Al2O3 surface stores more sulfur than that of BaO/Pt/Al2O3. BaO/Pt/CeO2/Al2O3 reveals a significantly improved thermal regeneration behavior in vacuum with respect to the conventional BaO/Pt/Al2O3 catalyst. Ceria promotion remarkably enhances the SO x reduction with H2(g).
Библиографическая ссылка: Say Z. , Vovk E.I. , Bukhtiyarov V.I. , Ozensoy E.
Enhanced Sulfur Tolerance of Ceria-Promoted NOx Storage Reduction (NSR) Catalysts: Sulfur Uptake, Thermal Regeneration and Reduction with H2(g)
Topics in Catalysis. 2013. V.56. N11. P.950-957. DOI: 10.1007/s11244-013-0059-5 WOS Scopus РИНЦ CAPlusCA OpenAlex Sciact
Файлы: Полный текст от издателя
Даты:
Опубликована online: 16 мая 2013 г.
Опубликована в печати: 1 авг. 2013 г.
Идентификаторы БД:
Web of science: WOS:000321664200012
Scopus: 2-s2.0-84880434226
РИНЦ: 20443545
Chemical Abstracts: 2013:766224
Chemical Abstracts (print): 159:139178
OpenAlex: W2153283586
Sciact: 1011
Цитирование в БД:
БД Цитирований
Web of science 11
Scopus 12
OpenAlex 12
Альметрики: