Assessing the acidity of high silica chabazite H-SSZ-13 by FTIR using CO as molecular probe: Comparison with H-SAPO-34

被引:142
作者
Bordiga, S
Regli, L
Cocina, D
Lamberti, C
Bjorgen, M
Lillerud, KP
机构
[1] Univ Oslo, Dept Chem, N-0315 Oslo, Norway
[2] IFM & NIS Ctr Excellence, Dipartimento Chim, I-10125 Turin, Italy
关键词
D O I
10.1021/jp045498w
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
Zeolitic materials based on the chabazite topology, such as H-SAPO-34, possess unique shape-selectivity properties for converting methanol into light olefins. In addition to the topology, zeolite acidity is inherently linked to catalyst activity and selectivity. The acidic properties of high silica chabazite (H-SSZ-13) have attracted much attention in the past decade because the material represents an idealized model system having one acidic site per cage. Conclusions drawn so far have essentially been founded on quantum chemical methods. An experimentally based benchmark of the acidity of H-SSZ-13 has hitherto not been available. In this work, transmission FTIR spectroscopy provides a description of the different acidic sites of H-SSZ-13 by using CO as molecular probe at 70 K. The results demonstrate that H-SSZ-13 is a strongly Bronsted acidic material, essentially having two distinct families of acidic sites. In contrast to numerous preceding reports, we find it fundamental to consider proton distributions among all four possible sites, and do not delimit the interpretations to only two sites. The present data consistently suggest the most abundant family of protons to have three members being located on different crystalline positions on the eight-membered-ring window giving access to the chabazite cage. Consequently, these protons are exposed to two neighboring cages. The second, and less abundant family, is constituted by only one site that is situated on the six-membered ring defining the top/bottom of the barrel-shaped chabazite cage. This proton is therefore only exposed to one cage and requires a higher CO pressure to form adducts. Toward CO, both families of sites possess the same acidity. Parallel experiments were also carried out for the isostructural and commercially important H-SAPO-34 having an equal density of acidic sites. This is the first attempt to directly compare, on an experimental basis, the acidity of these two materials.
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页码:2779 / 2784
页数:6
相关论文
共 48 条
[1]   Spectroscopic characterization of acidity in chabazite [J].
Aufdembrink, BA ;
Dee, DP ;
McDaniel, PL ;
Mebrahtu, T ;
Slager, TL .
JOURNAL OF PHYSICAL CHEMISTRY B, 2003, 107 (37) :10025-10031
[2]   Characterisation of defective silicalites [J].
Bordiga, S ;
Roggero, I ;
Ugliengo, P ;
Zecchina, A ;
Bolis, V ;
Artioli, G ;
Buzzoni, R ;
Marra, G ;
Rivetti, F ;
Spanò, G ;
Lamberti, C .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 2000, (21) :3921-3929
[3]   LOW-TEMPERATURE CO ADSORPTION ON NA-ZSM-5 ZEOLITES - AN FTIR INVESTIGATION [J].
BORDIGA, S ;
PLATERO, EE ;
AREAN, CO ;
LAMBERTI, C ;
ZECCHINA, A .
JOURNAL OF CATALYSIS, 1992, 137 (01) :179-185
[4]   FOURIER-TRANSFORM INFRARED STUDY OF CO ADSORBED AT 77-K ON H-MORDENITE AND ALKALI-METAL-EXCHANGED MORDENITES [J].
BORDIGA, S ;
LAMBERTI, C ;
GEOBALDO, F ;
ZECCHINA, A ;
PALOMINO, GT ;
AREAN, CO .
LANGMUIR, 1995, 11 (02) :527-533
[5]   Hydroxyls nests in defective silicalites and strained structures derived upon dehydroxylation:: vibrational properties and theoretical modelling [J].
Bordiga, S ;
Ugliengo, P ;
Damin, A ;
Lamberti, C ;
Spoto, G ;
Zecchina, A ;
Spanò, G ;
Buzzoni, R ;
Dalloro, L ;
Rivetti, F .
TOPICS IN CATALYSIS, 2001, 15 (01) :43-52
[6]   Adsorption of gases in multimolecular layers [J].
Brunauer, S ;
Emmett, PH ;
Teller, E .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1938, 60 :309-319
[7]  
CHEN J, 1994, STUD SURF SCI CATAL, V84, P1731
[8]   Cation selectivity in alkali-exchanged chabazite:: An ab initio periodic study [J].
Civalleri, B ;
Ferrari, AM ;
Llunell, M ;
Orlando, R ;
Mérawa, M ;
Ugliengo, P .
CHEMISTRY OF MATERIALS, 2003, 15 (21) :3996-4004
[9]   Acid strength of low-valence dopant ions in microporous zeolites and AlPOs [J].
Corà, F ;
Catlow, CRA ;
Civalleri, B ;
Orlando, R .
JOURNAL OF PHYSICAL CHEMISTRY B, 2003, 107 (43) :11866-11870
[10]  
CRANSTON RW, 1957, ADV CATAL, V9, P143