An investigation of the activity and stability of Pd and Pd-Zr modified Y-zeolite catalysts for the removal of PAH, CO, CH4 and NOx emissions

被引:24
作者
Klingstedt, F
Neyestanaki, AK
Lindfors, LE
Salmi, T
Heikkilä, T
Laine, E
机构
[1] Abo Akad Univ, Lab Ind Chem, Proc Chem Grp, FIN-20500 Turku, Finland
[2] Univ Turku, Dept Phys, Lab Ind Phys, FIN-20014 Turku, Finland
基金
芬兰科学院;
关键词
Pd-Y-zeolite; catalytic combustion of biofuels; de-activation (de-alumination); trapping;
D O I
10.1016/S0926-860X(02)00386-1
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
Pd-Y- and Pd-Zr-Y-zeolite catalysts were prepared by the ion-exchange of parent NH3-Y-zeolite, thermally pre-treated Y-zeolite and hydrothermally pre-treated Y-zeolite. The activity of the catalysts was studied in conversion of gas mixtures simulating the flue gases from the combustion of biofuels and natural gas driven vehicles (NGVs) at temperature ranges of 120-800 degreesC. The effect of sulphur-poisoning was examined by the addition of 5 ppm SO2 into the feed gas mixtures. High activity in the removal of the model pollutants was obtained over the fresh catalysts. De-activation was observed as a result of catalyst ageing in the reactants' flow (800degreesC, 6h) or steam treatment (850degreesC, 12 vol.% H2O, 16h). The de-activation was attributed to the de-alumination as well as to the migration of Pd2+ cations. The catalysts were characterised by XRD, SEM-EDXA, N-2-physisorption, O-2/SO2/NH3/naphthalene-TPD, XRF and DCP. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:229 / 240
页数:12
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