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Octahedral Layered Birnessite (OL) Supported Ag Catalysts: Characterization and Catalytic Oxidation of CO

机译:八面体分层Birniedite(OL)支持的Ag催化剂:CO的表征和催化氧化

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摘要

Octahedral layered birnessite (OL) was synthesized by redox method, and OL supported Ag catalysts (xAg/OL, x = 0.1wt%, 0.2wt%, 0.3wt%, 0.5wt%) were prepared by ion exchange method. Then catalysts were characterized by XRD, SEM, BET, H2-TPR, TG, O_2-TPD and in-situ DRIFTS, while the catalytic activity of CO was evaluated. Among xAg/OL samples, the 0.3Ag/OL exhibited the best catalytic activity for CO oxidation (T_(50) = 105°C and T_(90) = 135°C). The results show that the chemical adsorption of oxygen, the low-temperature reducibility and the strong interaction between the Ag species and OL are related to the excellent catalytic activity of xAg/OL. The reaction mechanism was studied by in-situ DRIFTS. First, O_2 was adsorbed and activated on the oxygen vacancies of xAg/OL, then formed oxygen free radical attacked the adsorbed CO and produced CO_2, subsequently CO_2 desorbed from the catalyst surface. Oxygen vacancies was supplemented by gas O_2, thus circulating.
机译:通过离子交换法制备通过离子交换法制备八氧化物方法(XAG / OL,X = 0.1wt%,0.2wt%,0.3wt%,0.2wt%,0.3wt%)合成的八半乳酸层(ol)。 然后通过XRD,SEM,BET,H 2-TPR,Tg,O_2-TPD和原位漂移表征催化剂,而评价了CO的催化活性。 在XAG / OL样品中,0.3Ag / OL表现出用于共氧化的最佳催化活性(T_(50)= 105℃和T_(90)= 135℃)。 结果表明,氧气的化学吸附,低温还原性和AG物种与OL之间的强相互作用与XAG / OL的优异催化活性有关。 通过原位漂移研究了反应机理。 首先,在XAG / OL的氧空位上吸附并激活O_2,然后形成氧自由基被侵入吸附的CO和产生的CO_2,随后从催化剂表面解吸。 氧气空位由气体O_2补充,从而循环。

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