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Low temperature complete combustion of methane over cobalt chromium oxides catalysts

机译:钴铬氧化物催化剂上甲烷的低温完全燃烧

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Cobalt chromium oxides with different Co/Cr ratios were prepared via co-precipitation method and their catalytic performances on methane combustion were evaluated from 300 ℃ to 650 ℃ at a space velocity of 36,000 h~(-1). A significant improvement of activity was observed over the Co1Cr2 catalyst with a Co/Cr molar ratio of 1:2, and the methane conversion reached 90% at 464 ℃. The Co1 Cr2 catalyst also showed excellent resistance to water vapor poisoning. In addition, the catalytic activity was inhibited in the presence of water vapor at the entire temperature range, while catalytic activity decreased only at low temperature in the presence of sulfur dioxide. Based on BET, TPR, XRD and XPS results, the superior performance of ColCr2 would origin from the higher valence and coordination number of the metal ions. Both Cr~(3+) and Cr~(6+) species were observed on the surface of cobalt chromites, and Cr~(6+) causes disorders in the spinel structure of cobalt chromites, which would enhance the adsorption of chemisorbed oxygen species and thus improve the catalytic performance, especially at low temperature.
机译:采用共沉淀法制备了不同Co / Cr比的钴铬氧化物,并在36,000 h〜(-1)的空速下,从300℃至650℃对它们的甲烷燃烧催化性能进行了评价。 Co / Cr摩尔比为1:2的Co1Cr2催化剂的活性明显提高,并且在464℃甲烷转化率达到90%。 Co1 Cr2催化剂还显示出优异的抗水蒸气中毒性。另外,在整个温度范围内在水蒸气存在下催化活性被抑制,而仅在低温下在二氧化硫存在下催化活性降低。根据BET,TPR,XRD和XPS结果,ColCr2的优异性能将源于金属离子的价数和配位数更高。在亚铬酸钴的表面均观察到Cr〜(3+)和Cr〜(6+)物种,并且Cr〜(6+)导致亚铬酸钴的尖晶石结构紊乱,从而增强了化学吸附氧物种的吸附。因此提高了催化性能,尤其是在低温下。

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