Pd-Ag/Al2O3 catalyst: Stages of deactivation in tail-end acetylene selective hydrogenation

被引:45
|
作者
Ravanchi, Maryam Takht [1 ]
Sahebdelfar, Saeed [1 ]
机构
[1] Natl Petrochem Co, Petrochem Res & Technol Co, Catalyst Res Grp, POB 14358-84711, Tehran, Iran
关键词
Acetylene hydrogenation; Pd-Ag/alpha-Al2O3; Catalyst deactivation; Coke formation; ETHENE-RICH STREAMS; PALLADIUM CATALYSTS; ETHYNE; REGENERATION; PERFORMANCE; KINETICS; ALUMINA; SIZE;
D O I
10.1016/j.apcata.2016.07.014
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The deactivation of a Pd-Ag/alpha-Al2O3. catalyst (2.5 mm in diameter, containing 0.03 wt.% Pd and 0.18 wt.% Ag) with egg-shell distribution was studied for acetylene selective hydrogenation. The reaction was performed in a fixed bed reactor using C2H2/C2H4/H-2 feed mixture (1:67.5:1.5 molar ratio). The long-term deactivation behaviour of the catalyst was studied by differential method of analysis using appropriate power law kinetics for the main reaction and catalyst decay. Based on the analysis of model results, it was proposed that the catalyst deactivation proceeded in two stages. The initial stage (Stage I) was relatively short (<20 h) and characterized by rapid catalyst deactivation, followed by second stage (Stage II) of much slower deactivation rate exhibiting a deactivation rate constant one order of magnitude smaller than Stage I. It was attributed to the dual role of carbonaceous deposits on catalyst that exhibited sequential activation and deactivation effects. The TG and FT-IR analysis of the spent catalyst revealed formation of aliphatic (soft) coke after about 100 h on stream. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:197 / 203
页数:7
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