Synthesis and crystal structure of As-synthesized and calcined pure silica zeolite ITQ-12

被引:57
作者
Yang, XB [1 ]
Camblor, MA
Lee, Y
Liu, HM
Olson, DH
机构
[1] Univ Penn, Dept Chem & Biomol Engn, Philadelphia, PA 19104 USA
[2] CSIC, Inst Ciencia Mat, Dept Mat Porosos & Compuestos Intercalac, E-28049 Madrid, Spain
[3] Brookhaven Natl Lab, Dept Phys, Upton, NY 11973 USA
[4] Atofina Chem Inc, King Of Prussia, PA 19406 USA
关键词
D O I
10.1021/ja0481474
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The small-pore pure silica zeolite ITQ-12 has been synthesized with fumed silica as the silica source in the presence of 1,3,4-trimethylimidazolium hydroxide and hydrofluoric acid under hydrothermal conditions at 448 K. Rietveld refinement using synchrotron X-ray diffraction data of the calcined ITQ-12 product taken at 298 K confirms the proposed topology, framework type code ITW, which can be described by a monoclinic unit cell [Si24O48] having Cm symmetry. Unit cell parameters are a = 10.3360(4), b = 15.0177(6), and c = 8.8639(4) Angstrom, beta = 105.356(3)degrees, and cell volume V = 1326.76(9) Angstrom(3). For as-synthesized ITQ-12, the occluded fluoride anion is located inside the double four-membered ring, while the flat 1,3,4-trimethylimidazolium cation lies on the equatorial plane of the slit-shaped [44546484] cage, with its longest dimension in the [010] direction. The monoclinic unit cell \(C6N2H11)+F-2(2)-\[Si24O48], having Cm symmetry, has parameters a = 10.4478(3), b = 14.9854(4), and c = 8.8366(3) Angstrom, beta = 105.935(2)degrees, and cell volume V= 1330.34(7) Angstrom(3) at 298 K. Cooperative structure-directing effects during the crystallization of ITQ-12 are discussed in terms of the structure of the as-made material.
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页码:10403 / 10409
页数:7
相关论文
共 28 条
[1]   Formation and stability of N-heterocyclic carbenes in water:: The carbon acid pKa of imidazollum cations in aqueous solution [J].
Amyes, TL ;
Diver, ST ;
Richard, JP ;
Rivas, FM ;
Toth, K .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (13) :4366-4374
[2]   ITQ-12: a new microporous silica polymorph potentially useful for light hydrocarbon separations [J].
Barrett, PA ;
Boix, T ;
Puche, M ;
Olson, DH ;
Jordan, E ;
Koller, H ;
Camblor, MA .
CHEMICAL COMMUNICATIONS, 2003, (17) :2114-2115
[3]   Crystal structure of zeolite MCM-35 (MTF) [J].
Barrett, PA ;
Díaz-Cabañas, MJ ;
Camblor, MA .
CHEMISTRY OF MATERIALS, 1999, 11 (10) :2919-2927
[4]  
Boix T., 2002, Patent No. 6471939
[5]   Synthesis and structure of ITQ-3, the first pure silica polymorph with a two-dimensional system of straight eight-ring channels [J].
Camblor, MA ;
Corma, A ;
Lightfoot, P ;
Villaescusa, LA ;
Wright, PA .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 1997, 36 (23) :2659-2661
[6]   Synthesis of all-silica and high-silica molecular sieves in fluoride media [J].
Camblor, MA ;
Villaescusa, LA ;
Díaz-Cabañas, MJ .
TOPICS IN CATALYSIS, 1999, 9 (1-2) :59-76
[7]   High silica zeolites with three-dimensional systems of large pore channels [J].
Camblor, MA ;
Barrett, PA ;
Díaz-Cabañas, MJ ;
Villaescusa, LA ;
Puche, M ;
Boix, T ;
Pérez, E ;
Koller, H .
MICROPOROUS AND MESOPOROUS MATERIALS, 2001, 48 (1-3) :11-22
[8]  
CAULLET P, 1991, EUR J SOL STATE INOR, V28, P345
[9]   ZEOLITE AND MOLECULAR-SIEVE SYNTHESIS [J].
DAVIS, ME ;
LOBO, RF .
CHEMISTRY OF MATERIALS, 1992, 4 (04) :756-768
[10]   Synthesis and structure of pure SiO2 chabazite:: the SiO2 polymorph with the lowest framework density [J].
Díaz-Cabañas, MJ ;
Barrett, PA ;
Camblor, MA .
CHEMICAL COMMUNICATIONS, 1998, (17) :1881-1882