Pd-Ag/-Al2O3 Catalyst Deactivation in Acetylene Selective Hydrogenation Process

被引:30
|
作者
Ravanchi, Maryam Takht [1 ]
Sahebdelfar, Saeed [1 ]
Fard, Maryam Rahimi [1 ]
Fadaeerayeni, Siavash [1 ]
Bigdeli, Peyman [2 ]
机构
[1] Natl Petrochem Co, Petrochem Res & Technol Co, Catalyst Res Grp, POB 14358-84711, Tehran, Iran
[2] Natl Petrochem Co, Petrochem Res & Technol Co, Gas Chromatog Lab, Tehran, Iran
关键词
Acetylene hydrogenation; Catalyst deactivation; Coke formation; Kinetic model; Pd-Ag; -Al2O3; catalyst; ETHENE-RICH STREAMS; PALLADIUM CATALYSTS; PD-AG/AL2O3; CATALYSTS; PD/AL2O3; CATALYST; PD CATALYSTS; PERFORMANCE; ETHYNE; ETHYLENE; ALUMINA; MODEL;
D O I
10.1002/ceat.201400526
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The selective hydrogenation of acetylene to ethylene over Pd-Ag/-Al2O3 catalysts prepared by different impregnation/reduction methods was studied. The best catalytic performance was achieved with the sample prepared by sequential impregnation. A kinetic model based on first order in acetylene and 0.5th order in hydrogen for the main reaction and second-order independent decay law for catalyst deactivation was used to fit the conversion time data and to obtain quantitative assessment of catalyst performances. Fair fits were observed from which the reaction and deactivation rate constants were evaluated. Coke deposition amounts showed a good correlation with catalyst deactivation rate constants, indicating that coke formation should be the main cause of catalyst deactivation.
引用
收藏
页码:301 / 310
页数:10
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