Structure and properties of cobalt-exchanged H-ZSM5 catalysts for dehydrogenation and dehydrocyclization of alkanes

被引:94
作者
Li, W
Yu, SY
Meitzner, GD
Iglesia, E [1 ]
机构
[1] Univ Calif Berkeley, Dept Chem Engn, Berkeley, CA 94720 USA
[2] Edge Analyt, Middleton, WI 53562 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 2001年 / 105卷 / 06期
关键词
D O I
10.1021/jp002102h
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
Co/H-ZSM5 catalysts with Co/Al ratios of 0.09-0.22 were prepared by aqueous exchange. Turnover rates for propane conversion to propene and to C-6-C-8 aromatics on these catalysts are about 10-fold higher than on H-ZSM5. The selectivities to propene, aromatics, and H-2 are also higher on Co/H-ZSM5 than on H-ZSM5. The rate of D-2 exchange with OH groups increases with increasing Co/Al ratio, suggesting that Co cations catalyze D-2 dissociative chemisorption steps that limit the rate of isotopic exchange. Co cations also catalyze hydrogen recombinative desorption steps, which limit the rate of propane dehydrogenation and aromatization reactions. The density of residual zeolitic hydroxyls was measured by D-2-OB isotopic exchange and by changes in the intensity of OH infrared bands as a function of Co content. D-2-OH and infrared measurements showed that Co2+ cations replace 1.1-1.3 zeolitic protons, suggesting the predominant presence of Co2+- O-Co2+ dimers, with some Co2+ monomers, each bridging two next-nearest neighbor Al sites. The location and structure of exchanged Co cations were probed using X-ray absorption spectroscopy (XAS) and temperature-programmed reduction (TPR). No Hz consumption was detected up to 1273 K during TPR in any of the Co/H-ZSM5 samples, consistent with the absence of CoOx crystallites, which reduce at similar to 800 K. In situ near-edge X-ray absorption studies confirmed that Co species remain as divalent cations during exposure to H-2 or C3H8 at 773 K. Near-edge and fine structure analysis detected Co2+ cations with similar structure in all Co/H-ZSM5 samples (Co/Al < 0.22), and Co coordination changes from octahedral to tetrahedral upon sample dehydration at 773 K in He. Radial structure functions showed weak contributions from the first and second shells around Co. This reflects the nonunifomm nature of the distance and orientation in Al-Al next-nearest neighbor sites in ZSM5.
引用
收藏
页码:1176 / 1184
页数:9
相关论文
共 31 条
[1]  
BARTON DG, 1998, THESIS U CALIFORNIA
[2]   REEVALUATION OF X-RAY ATOMIC ENERGY LEVELS [J].
BEARDEN, JA ;
BURR, AF .
REVIEWS OF MODERN PHYSICS, 1967, 39 (01) :125-&
[3]   Structure and function of metal cations in light alkane reactions catalyzed by modified H-ZSM5 [J].
Biscardi, JA ;
Iglesia, E .
CATALYSIS TODAY, 1996, 31 (3-4) :207-231
[4]   Structure and density of active Zn species in Zn/H-ZSM5 propane aromatization catalysts [J].
Biscardi, JA ;
Meitzner, GD ;
Iglesia, E .
JOURNAL OF CATALYSIS, 1998, 179 (01) :192-202
[5]   Non-oxidative reactions of propane on Zn/Na-ZSM5 [J].
Biscardi, JA ;
Iglesia, E .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 1999, 1 (24) :5753-5759
[6]   Isotopic tracer studies of propane reactions on H-ZSM5 zeolite [J].
Biscardi, JA ;
Iglesia, E .
JOURNAL OF PHYSICAL CHEMISTRY B, 1998, 102 (46) :9284-9289
[7]   Reaction pathways and rate-determining steps in reactions of alkanes on H-ZSM5 and Zn/H-ZSM5 catalysts [J].
Biscardi, JA ;
Iglesia, E .
JOURNAL OF CATALYSIS, 1999, 182 (01) :117-128
[8]   Structure and density of Mo and acid sites in Mo-exchanged H-ZSM5 catalysts for nonoxidative methane conversion [J].
Borry, RW ;
Kim, YH ;
Huffsmith, A ;
Reimer, JA ;
Iglesia, E .
JOURNAL OF PHYSICAL CHEMISTRY B, 1999, 103 (28) :5787-5796
[9]   Dealumination of HZSM-5 zeolites .1. Calcination and hydrothermal treatment [J].
Campbell, SM ;
Bibby, DM ;
Coddington, JM ;
Howe, RF ;
Meinhold, RH .
JOURNAL OF CATALYSIS, 1996, 161 (01) :338-349
[10]   Co-ZSM-5 catalysts for N2O decomposition [J].
da Cruz, RS ;
Mascarenhas, AJS ;
Andrade, HMC .
APPLIED CATALYSIS B-ENVIRONMENTAL, 1998, 18 (3-4) :223-231