Polynuclear Co-oxo cations in the catalytic oxidation of CO on Co-modified ZSM-5 zeolites

Shilina, M.I.; Rostovshchikova, T.N.; Nikolaev, S.A.; Udalova, O.V.

Авторы: Shilina M.I., Rostovshchikova T.N., Nikolaev S.A., Udalova O.V.
Журнал: Materials Chemistry and Physics
Том: 223
Год издания: 2019
Издательство: Elsevier BV
Местоположение издательства: Netherlands
Первая страница: 287
Последняя страница: 298
DOI: 10.1016/j.matchemphys.2018.11.005
Аннотация: Structure, reducibility and catalytic activity in the oxidation of CO were studied for Co-modified ZSM-5 zeolites (Co/Al = 0.1–0.9) prepared via impregnation, solid-state and wet ion exchange. According to TEM, XPS, DRIFTS, UV–vis-DRS, H2 -TPR and in situ CO- reduction studies the synthesis method and the Co content affect the surface distribution of Co as Со2+ ions, cationic oxo-complexes and highly dispersed CoxOy species. The oxidation of CO by oxygen was studied at 50–450 °C in pulse and flow regimes at the 2:1 and 1:1 CO:O2 ratios. Co-zeolites prepared by impregnation were the most active in the oxidation of CO. It was proposed that oxo cations [CoxOy]n+ (n = 1, 2) with Co(III) prevailing in their structure play a crucial role in CO adsorption and catalytic oxidation. The new absorption band at 2215 cm−1 attributed to CO adsorbed on the Co(III) located in oxo cations was found. These oxo-cations contain a mobile oxygen atoms and, thus, can be easily reduced to the catalytically active Сo3+/Сo2+and Сo2+/Сo+ pairs stabilized in zeolites. In contrast to the supported catalysts based on Co3O4, the activity of Co-ZSM-5 increased during the reaction, and the light-off T50 drifted to 120 °C.
Добавил в систему: Шилина Марина Ильинична

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Polynuclear Co-oxo cations in the catalytic oxidation of CO on Co-modified ZSM-5 zeolitesстатья

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