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Selective oxidation of CO in the presence of propylene over Ag/MCM-41 catalyst G. V. Mamontov, A. S. Gorbunova, E. V. Vyshegorodtseva [et al.]

Contributor(s): Gorbunova, A. S | Vyshegorodtseva, E. V | Zaikovskii, Vladimir I | Mamontov, Grigory V | Vodyankina, Olga VMaterial type: ArticleArticleSubject(s): селективное окисление | монооксид углерода | катализаторы | очистка пропиленаGenre/Form: статьи в журналах Online resources: Click here to access online In: Catalysis today Vol. 333. P. 245-250Abstract: Ag/MCM-41 catalyst is prepared by impregnation technique and characterized by low-temperature N2 sorption, XRD, TPR and TEM methods. The ordered structure of mesoporous silicate MCM-41 is used as a nanoreactor to synthesize and stabilize small Ag nanoparticles. Two types of Ag particles are shown to form in Ag/MCM-41 catalyst: ultrasmall (<3 nm) inside pores of support and large (4–8 nm) on the external surface of the MCM-41. Catalytic tests in oxidation mixture containing 1% CO and 1% propylene show that Ag/MCM-41 catalyst can be used for selective oxidation of CO in the presence of propylene from 91 °C (CO conversion > 98%) to 217 °C (conversion of propylene < 5%). The catalyst can be used for purification of hydrocarbons from CO by selective oxidation of second.
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Библиогр.: 65 назв.

Ag/MCM-41 catalyst is prepared by impregnation technique and characterized by low-temperature N2 sorption, XRD, TPR and TEM methods. The ordered structure of mesoporous silicate MCM-41 is used as a nanoreactor to synthesize and stabilize small Ag nanoparticles. Two types of Ag particles are shown to form in Ag/MCM-41 catalyst: ultrasmall (<3 nm) inside pores of support and large (4–8 nm) on the external surface of the MCM-41. Catalytic tests in oxidation mixture containing 1% CO and 1% propylene show that Ag/MCM-41 catalyst can be used for selective oxidation of CO in the presence of propylene from 91 °C (CO conversion > 98%) to 217 °C (conversion of propylene < 5%). The catalyst can be used for purification of hydrocarbons from CO by selective oxidation of second.

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