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首页> 外文期刊>Applied Catalysis, A. General: An International Journal Devoted to Catalytic Science and Its Applications >HIGH SURFACE AREA ALPHA-ALUMINAS .3. OXIDATION OF ETHYLENE, ETHYLENE OXIDE, AND ACETALDEHYDE OVER SILVER DISPERSED ON HIGH SURFACE AREA ALPHA-ALUMINA
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HIGH SURFACE AREA ALPHA-ALUMINAS .3. OXIDATION OF ETHYLENE, ETHYLENE OXIDE, AND ACETALDEHYDE OVER SILVER DISPERSED ON HIGH SURFACE AREA ALPHA-ALUMINA

机译:高表面积Alpha-Aluminums.3。分散在高表面积铝矾土上的银上的乙烯,环氧乙烷和乙醛的氧化

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Silver nanocrystallites dispersed on high surface area (HSA) alpha-alumina were prepared, and the activity and selectivity to ethylene oxide (EO) during ethylene oxidation over these catalysts were determined in the absence of Cl promoters. Cesium was also added to some of the samples to neutralize any surface acidity. Over all the Ag/(HSA) alpha-Al2O3 catalysts, the selectivity to EO was negligible regardless of the addition of cesium while the apparent activation energy for carbon dioxide formation of 110 kJ mol(-1) over the unpromoted samples was higher than that of 80 kJ mol(-1) over a low surface area (LSA) alpha-alumina-supported silver catalyst. When this latter catalyst with selectivity to EO was mixed with (HSA) alpha-Al2O3, only carbon dioxide and water were obtained as a final product. EO isomerization and oxidation as well as acetaldehyde oxidation were also studied, and both silver and the support were found to be active in these reactions; hence these (HSA) alpha-aluminas are poor supports for ethylene epoxidation. In contrast to a promoting effect obtained at low concentrations in commercial catalysts, the higher loadings of cesium on these Ag/(HSA) alpha-Al2O3 catalysts increased the turnover frequency of ethylene oxidation as well as the rates of EO and acetaldehyde oxidation, while the apparent activation energy for ethylene combustion decreased to 80 kJ mol(-1) in the presence of cesium. [References: 27]
机译:制备了分散在高表面积(HSA)α-氧化铝上的银纳米晶体,并在不存在Cl助催化剂的情况下,测定了这些催化剂在乙烯氧化过程中对环氧乙烷(EO)的活性和选择性。铯也被添加到一些样品中和任何表面酸度。在所有的Ag /(HSA)α-Al2O3催化剂上,无论添加铯如何,对EO的选择性都可以忽略不计,而在未助催化的样品上形成110 kJ mol(-1)的二氧化碳的表观活化能比80 kJ mol(-1)在低表面积(LSA)α-氧化铝负载的银催化剂上的摩尔比。当将后一种对EO具有选择性的催化剂与(HSA)α-Al2O3混合时,仅获得二氧化碳和水作为最终产物。还研究了EO异构化和氧化以及乙醛氧化,发现银和载体在这些反应中均具有活性。因此,这些(HSA)α-氧化铝是乙烯环氧化的不良载体。与在商用催化剂中低浓度获得促进作用相反,这些Ag /(HSA)α-Al2O3催化剂上较高的铯负载量增加了乙烯氧化的转化频率以及EO和乙醛的氧化速率,而在铯存在下,乙烯燃烧的表观活化能降至80 kJ mol(-1)。 [参考:27]

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