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Temperature-Programmed Surface Reaction Study of Adsorption and Reaction of H2S on Ceria

机译:二氧化铈吸附和反应H2s的程序升温表面反应研究

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摘要

H2S adsorption and reaction on CeO2, TiO2, and gamma-Al2O3 were studied by temperature programmed surface reaction (TPSR). Ceria had the best desulfidation ability. The pretreatment atmosphere affected H2S adsorption and reaction on ceria, and desulfidation efficiency increased in the order of inert atmosphere, reducing atmosphere, oxidizing atmosphere. H2S was first adsorbed on pretreated ceria at room temperature. On increasing the temperature in an Ar (99.99%) atmosphere, part of the H2S desorbed below 673 K, and another part reacted with the surface oxygen on ceria to produce sulfur and water below 473 K, and SO2 between 473 and 673 K, which further reacted with lattice oxygen and was transformed into sulfate above 673 K. The sulfate decomposed into SO2 again at 873 K. To avoid the complex regeneration, it is advisable to carry out desulfidation below 673 K when using ceria as adsorbent.
机译:通过程序升温表面反应(TPSR)研究了硫化氢在CeO2,TiO2和γ-Al2O3上的吸附和反应。二氧化铈具有最佳的脱硫能力。预处理气氛影响H2S在二氧化铈上的吸附和反应,脱硫效率按惰性气氛,还原气氛,氧化气氛的顺序增加。首先在室温下将H2S吸附到预处理的氧化铈上。在Ar(99.99%)气氛中升高温度时,一部分H2S在673 K以下解吸,另一部分与二氧化铈上的表面氧反应生成473 K以下的硫和水,以及473至673 K之间的SO2。进一步与晶格氧反应,然后在673 K以上转化为硫酸盐。硫酸盐在873 K处再次分解为SO2。为避免复杂的再生,建议在使用二氧化铈作为吸附剂时在673 K以下进行脱硫。

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