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首页> 外文期刊>Applied Catalysis, B. Environmental: An International Journal Devoted to Catalytic Science and Its Applications >Sulfur poisoning of molybdenum dioxide during the partial oxidation of a Jet-A fuel surrogate
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Sulfur poisoning of molybdenum dioxide during the partial oxidation of a Jet-A fuel surrogate

机译:Jet-A燃料替代品的部分氧化过程中二氧化钼的硫中毒

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摘要

The aim of the present work is to investigate the effect that organic sulfur compounds have on the catalytic performance of molybdenum dioxide (MoO2) during the partial oxidation reaction of aviation fuels. N-dodecane and benzothiophene were used as surrogates for Jet-A fuel and as a model sulfur compound, respectively. Activity tests of commercial MoO2 toward the partial oxidation reaction of this model Jet-A fuel were performed at 850 °C Our studies indicate that MoO2 displays a remarkable tolerance to deactivation by organic sulfur compounds even at concentrations as high as 1000 ppmw, a typical sulfur concentration found in aviation fuels. However, commercial MoO2 catalysts show a significant catalytic performance deactivation as the concentration of organic sulfur compounds increases to 3000 ppmw. TEM and XPS data indicate that the deactivation process starts with the formation of Mo sulfide on the catalyst surface. The sulfide phase appears to reduce the ability of the catalyst to activate hydrocarbon molecules as well as impeding the ability to deliver lattice oxygen to the active surface sites, which leads to the enhancement of side reactions that promote the formation of coking. The catalyst deactivation resulting from the exposure to such high concentrations of organic sulfur compounds appears to be reversible with an air treatment at 850 °C The catalyst activity of MoO2 recovers approximately 80% of its initial performance as demonstrated by the H2 yield and TEM data.
机译:本工作的目的是研究在航空燃料的部分氧化反应中有机硫化合物对二氧化钼(MoO2)催化性能的影响。正十二烷和苯并噻吩分别用作Jet-A燃料的替代物和模型硫化合物。商业型MoO2对这种型号Jet-A燃料的部分氧化反应的活性测试是在850°C进行的。我们的研究表明,即使在浓度高达1000 ppmw(典型的硫)下,MoO2对有机硫化合物的失活表现出显着的耐受性。航空燃料中的浓度。然而,当有机硫化合物的浓度增加到3000 ppmw时,商用MoO2催化剂显示出明显的催化性能失活。 TEM和XPS数据表明,失活过程始于在催化剂表面形成硫化钼。硫化物相似乎降低了催化剂活化烃分子的能力,并阻碍了将晶格氧输送到活性表面位点的能力,这导致副反应增强,从而促进了焦化的形成。暴露于如此高浓度的有机硫化合物导致的催化剂失活在850°C的空气处理中似乎是可逆的。MoO2的催化剂活性恢复了其初始性能的80%,如H2收率和TEM数据所示。

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