负载铑催化剂的原位研究

P. Johnston, R. Joyner, P. Pudney, E. S. Shpiro, B. Williams
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引用次数: 24

摘要

以γ-氧化铝、氧化钒、铬和钼为载体制备了铑催化剂。研究了这些材料在合成气(H2/CO: 1/ 1,523 K, 5 bar压力)转化为甲醇、乙醇和碳氢化合物时的活性和选择性。除chromia外,所有催化剂均表现出相似的活性,在所选温度下几乎无活性。对高氧化合物的选择性为:V2O3 > MoO3 > Al2O3 > Cr2O3。氧化铝负载型催化剂对甲醇的选择性最高。通过扩展x射线吸收精细结构(EXAFS)对催化剂进行了原位表征,并对氧化铝支撑材料进行了最详细的研究。在473 K还原时,铑颗粒直径为30a,在铬载体上。讨论了催化剂结构与性能的关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In situ studies of supported rhodium catalysts
Rhodium catalysts have been prepared, supported on γ-alumina, vanadium(III) oxide, chromia and molybdena. The activity and selectivity of these materials in the conversion of synthesis gas, (H2/CO: 1/1, 523 K and 5 bar pressure), to methanol, ethanol and hydrocarbons has been studied. All catalysts showed similar activity except for chromia, which was almost inactive at the temperature chosen. Selectivity to higher oxygenates followed the trend: V2O3 > MoO3 > Al2O3 > Cr2O3. The alumina supported catalysts had the highest selectivity to methanol. Catalysts have been characterised in situ by extended X-ray absorption fine structure (EXAFS) and the alumina-supported material has been examined in the greatest detail. On reduction at 473 K, rhodium particles with diameter 30 A diameter, on the chromia support.The relation between catalyst structure and performance is discussed.
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