Ti location in the MFI framework of Ti-silicalite-1:: A neutron powder diffraction study

被引:170
作者
Lamberti, C
Bordiga, S
Zecchina, A
Artioli, G
Marra, G
Spanò, G
机构
[1] Univ Turin, Dipartimento Chim, IFM, I-10125 Turin, Italy
[2] Univ Turin, INFM, Unita Torino, I-10125 Turin, Italy
[3] Univ Milan, Dipartimento Sci Terra, I-20133 Milan, Italy
[4] CNR, Ctr Studio Geodinam Alpina & Quaternaria, I-20133 Milan, Italy
[5] EniChem SPA, Ist G Donegani, Ctr Ric Novara, I-28100 Novara, Italy
关键词
D O I
10.1021/ja003657t
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The first direct evidence that Ti atoms are not equally distributed in the 12 crystallographically independent T sites of the MFI framework is presented on the basis of neutron diffraction data collected at the HRPD instrument of the ISIS pulsed neutron source. We found strong evidence indicating that T6, T7, and T11 are the most populated sites and weak evidence that Ti may be hosted in T10. Ti occupancy can be excluded for sites T1, T2, T4, T5, T9, and T12. The occupancy of the remaining sites is doubtful. Since defective silicalite has been shown to exhibit the same preferential sites (T6, T7, T11, and T10) for Si vacancies, it may be suggested that the incorporation mechanism of the Ti atoms in the MFI framework occurs via the insertion of titanium in the defective sites. This hypothesis implies that titanium has a mineralizing effect on the MR framework, and it is supported by independent spectroscopic data on both TS-1 and defective silicalite. The results are discussed in comparison with the known substitution mechanisms in the T-sites of MFI-type structures.
引用
收藏
页码:2204 / 2212
页数:9
相关论文
共 60 条
[1]   Neutron powder diffraction study of orthorhombic and monoclinic defective silicalite [J].
Artioli, G ;
Lamberti, C ;
Marra, GL .
ACTA CRYSTALLOGRAPHICA SECTION B-STRUCTURAL SCIENCE, 2000, 56 (01) :2-10
[2]   REACTIONS OF TITANIUM SILICALITE WITH PROTIC MOLECULES AND HYDROGEN-PEROXIDE [J].
BELLUSSI, G ;
CARATI, A ;
CLERICI, MG ;
MADDINELLI, G ;
MILLINI, R .
JOURNAL OF CATALYSIS, 1992, 133 (01) :220-230
[3]   TI-47-49 NMR OF SOME TITANIUM COMPOUNDS [J].
BERGER, S ;
BOCK, W ;
MARTH, CF ;
RAGUSE, B ;
REETZ, MT .
MAGNETIC RESONANCE IN CHEMISTRY, 1990, 28 (06) :559-560
[4]   THE STATE OF TI IN TITANOALUMINOSILICATES ISOMORPHOUS WITH ZEOLITE-BETA [J].
BLASCO, T ;
CAMBLOR, MA ;
CORMA, A ;
PEREZPARIENTE, J .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1993, 115 (25) :11806-11813
[5]  
Boccuti M.R., 1989, STUD SURF SCI CATAL, P133
[6]   Heterogeneity of framework Ti(IV) in Ti-silicalite as revealed by the adsorption of NH3.: Combined calorimetric and spectroscopic study [J].
Bolis, V ;
Bordiga, S ;
Lamberti, C ;
Zecchina, A ;
Carati, A ;
Rivetti, F ;
Spanò, G ;
Petrini, G .
LANGMUIR, 1999, 15 (18) :5753-5764
[7]   A calorimetric, IR, XANES and EXAFS study of the adsorption of NH3 on Ti-silicalite as a function of the sample pre-treatment [J].
Bolis, V ;
Bordiga, S ;
Lamberti, C ;
Zecchina, A ;
Carati, A ;
Rivetti, F ;
Spanò, G ;
Petrini, G .
MICROPOROUS AND MESOPOROUS MATERIALS, 1999, 30 (01) :67-76
[8]   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
[9]   XAFS STUDY OF TI-SILICALITE - STRUCTURE OF FRAMEWORK TI(IV) IN PRESENCE AND IN ABSENCE OF REACTIVE MOLECULES (H2O, NH3) [J].
BORDIGA, S ;
BOSCHERINI, F ;
COLUCCIA, S ;
GENONI, F ;
LAMBERTI, C ;
LEOFANTI, G ;
MARCHESE, L ;
PETRINI, G ;
VLAIC, G ;
ZECCHINA, A .
CATALYSIS LETTERS, 1994, 26 (1-2) :195-208
[10]   XAFS STUDY OF TI-SILICALITE - STRUCTURE OF FRAMEWORK TI(IV) IN THE PRESENCE AND ABSENCE OF REACTIVE MOLECULES (H2O, NH3) AND COMPARISON WITH ULTRAVIOLET-VISIBLE AND IR RESULTS [J].
BORDIGA, S ;
COLUCCIA, S ;
LAMBERTI, C ;
MARCHESE, L ;
ZECCHINA, A ;
BOSCHERINI, F ;
BUFFA, F ;
GENONI, F ;
LEOFANTI, G ;
PETRINI, G ;
VLAIC, G .
JOURNAL OF PHYSICAL CHEMISTRY, 1994, 98 (15) :4125-4132