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首页> 外文期刊>Applied Catalysis, B. Environmental: An International Journal Devoted to Catalytic Science and Its Applications >Microwave-assisted integration of transition metal oxide nanocoatings on manganese oxide nanoarray monoliths for low temperature CO oxidation
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Microwave-assisted integration of transition metal oxide nanocoatings on manganese oxide nanoarray monoliths for low temperature CO oxidation

机译:低温共氧化锰氧化物纳米阵列锰氧化物纳米型过渡金属氧化物纳米织物的微波辅助整合

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摘要

Manganese oxide (OMS-2), a promising exhaust treatment catalyst, has been successfully integrated onto the channel wall surfaces of cordierite honeycombs in the form of a nanoarray forest. To further improve their catalytic carbon monoxide (CO) oxidation activity, a series of different metal oxide nanocoatings were uniformly grown on the surface of OMS-2 nanoarrays by utilizing a facile and fast microwave-assisted synthesis method. The manganese-cobalt oxide core-shell nanoarray based monolithic catalysts exhibit the highest catalytic performance with a 100% CO conversion at 150 degrees C, in a sharp contrast with 325 degrees C for the bare OMS-2 nanoarrays. Different growth mechanisms of the layered Co(OH)(2) and spinel Co3O4 induced by different cobalt precursors are used to explain the morphology evolution of the manganese-cobalt oxide core-shell nanoarrays. The Co3+ distributed on the surface of the nanoarrays acts as the active sites for CO oxidation. The small grain size, abundant surface-adsorbed oxygen, and interfacial effects between MnO2 and Co3O4 were found to favor the observed high catalytic activity. A thermal annealing study showed that high temperature induces the sintering of the nanoarray catalyst, which further affects the CO oxidation activity. This fast, cost-effective, and scalable method will provide a new route for synthesizing efficient core-shell nanoarray monolithic catalysts for low temperature catalysis.
机译:氧化锰(OMS-2)是一种有前途的排气处理催化剂,已成功地集成到纳米阵列森林的形式的堇青石蜂窝状的通道壁表面上。为了进一步改善其催化碳一氧化物(CO)氧​​化活性,通过利用容易和快速的微波辅助合成方法,将一系列不同的金属氧化物纳米织物均匀地生长在OMS-2纳米阵列的表面上。锰 - 钴氧化物核 - 壳纳米阵列的整体式催化剂在150℃下具有100%CO转化的最高催化性能,以325℃对于裸OMS-2纳米阵列的325℃。由不同钴前体诱导的层状CO(OH)(2)和尖晶石CO3O4的不同生长机制用于解释锰 - 钴氧化物核心壳纳米阵列的形态学化。分布在纳米阵列表面上的CO 3 +作为共同氧化的活​​性位点。发现小晶粒尺寸,丰富的表面吸附的氧气和MNO2和CO 3O4之间的界面效应有利于观察到的高催化活性。热退火研究表明,高温诱导纳米阵列催化剂的烧结,这进一步影响了共氧化活性。这种快速,成本效益和可伸缩的方法将提供一种用于合成高效核 - 壳纳米阵列整体催化剂的新途径,用于低温催化。

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