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

被引：2

作者：

Liu Bing ^{[1
,2
,3
]}

Xu Hengyong ^{[1
]}

Zhang Zehui ^{[2
,3
]}

机构：

[1] Chinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Liaoning, Peoples R China

[2] S Cent Univ Nationalities, Coll Chem & Mat Sci, Key Lab Catalysis & Mat Sci, State Ethn Affairs Commiss, Wuhan 430074, Hubei, Peoples R China

[3] S Cent Univ Nationalities, Coll Chem & Mat Sci, Minist Educ, Wuhan 430074, Hubei, Peoples R China

来源：

CHINESE JOURNAL OF CATALYSIS | 2012年 / 33卷 / 10期

关键词：

ceria; hydrogen sulfide; adsorption; temperature-programmed surface reaction; GAS-SHIFT REACTION; HYDROGEN-SULFIDE; SULFUR; CATALYSTS; REMOVAL;

D O I：

10.1016/S1872-2067(11)60416-6

中图分类号：

O69 [应用化学];

学科分类号：

081704 ;

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.

引用

页码：1631 / 1635

页数：5

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