First unseeded hydrothermal synthesis of microporous vanadosilicate AM-6

被引:22
作者
Ismail, Mariam N. [1 ]
Fraiman, Naftali D. [1 ]
Callahan, Dennis M., Jr. [1 ]
Gursoy, Gamze [1 ]
Viveiros, Edward [1 ]
Ozkanat, Onnaz [1 ]
Ji, Zhaoxia [1 ]
Willey, Ronald J. [1 ]
Warzywoda, Juliusz [1 ]
Sacco, Albert, Jr. [1 ]
机构
[1] Northeastern Univ, Dept Chem Engn, Boston, MA 02115 USA
关键词
AM-6; Morphology; Surface structure; Synthesis; Vanadosilicates; MOLECULAR-SIEVE SYNTHESIS; VANADIUM-OXIDE CATALYSTS; TITANIUM SILICATE ETS-10; TITANOSILICATE ETS-10; CRYSTAL-STRUCTURE; CRYSTALLIZATION; ZEOLITE; FRAMEWORK; TETRAMETHYLAMMONIUM; SUBSTITUTION;
D O I
10.1016/j.micromeso.2008.12.020
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Microporous vanadosilicate AM-6 has been hydrothermally synthesized for the first time in the absence of titanosilicate ETS-10 seeds. High purity (95-100% AM-6) products were crystallized under static conditions at 430-503 K using tetramethylammonium hydroxide (TMAOH) or tetramethylammonium bromide (TMABr) as a structure-directing agent in mixtures with molar compositions xNa(2)O: 1.3K(2)O:ySiO(2):0.5V(2)O(5):wTMA:zH(2)O, where x = 4.5 or 5.6, y = 4.3-5.5, w = 2.0-3.0, and z = 206-214. The size (similar to 250 nm to similar to 9 mu m range), truncated square bipyramidal morphology (varied from square cuboid to thin (thickness <100-200 nm) tetragonal platy), and surface irregularities/faulting of AM-6 crystals (Si/V = 5.0 +/- 0.5) can be controlled by varying the molar composition or initial pH of synthesis mixture, and crystallization temperature. Structure-directing agent can be removed from the pores with little or no adverse effects on crystallinity of AM-6 by treatment with gaseous ammonia at elevated temperatures. UV-vis and FTIR analyses suggest two (V4+, V5+) oxidation states of vanadium in the AM-6 framework. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:454 / 459
页数:6
相关论文
共 48 条
[1]   MICROPOROUS TITANOSILICATE ETS-10 - A STRUCTURAL SURVEY [J].
ANDERSON, MW ;
TERASAKI, O ;
OHSUNA, T ;
MALLEY, PJO ;
PHILIPPOU, A ;
MACKAY, SP ;
FERREIRA, A ;
ROCHA, J ;
LIDIN, S .
PHILOSOPHICAL MAGAZINE B-PHYSICS OF CONDENSED MATTER STATISTICAL MECHANICS ELECTRONIC OPTICAL AND MAGNETIC PROPERTIES, 1995, 71 (05) :813-841
[2]   STRUCTURE OF THE MICROPOROUS TITANOSILICATE ETS-10 [J].
ANDERSON, MW ;
TERASAKI, O ;
OHSUNA, T ;
PHILIPPOU, A ;
MACKAY, SP ;
FERREIRA, A ;
ROCHA, J ;
LIDIN, S .
NATURE, 1994, 367 (6461) :347-351
[3]   Growth models in microporous materials [J].
Anderson, MW ;
Agger, JR ;
Hanif, N ;
Terasaki, O .
MICROPOROUS AND MESOPOROUS MATERIALS, 2001, 48 (1-3) :1-9
[4]   MCM-48-supported vanadium oxide catalysts, prepared by the molecular designed dispersion of VO(acac)2:: A detailed study of the highly reactive MCM-48 surface and the structure and activity of the deposited VOx [J].
Baltes, M ;
Cassiers, K ;
Van Der Voort, P ;
Weckhuysen, BM ;
Schoonheydt, RA ;
Vansant, EF .
JOURNAL OF CATALYSIS, 2001, 197 (01) :160-171
[5]  
Brandao P, 2003, EUR J INORG CHEM, P1175
[6]   MECHANISM OF STRUCTURE DIRECTION IN THE SYNTHESIS OF SI-ZSM-5 - AN INVESTIGATION BY INTERMOLECULAR H-1-SI-29 CP MAS NMR [J].
BURKETT, SL ;
DAVIS, ME .
JOURNAL OF PHYSICAL CHEMISTRY, 1994, 98 (17) :4647-4653
[7]   Supported vanadium oxide catalysts:: Quantitative spectroscopy, preferential adsorption of V4+/5+, and Al2O3 coating of zeolite Y [J].
Catana, G ;
Rao, RR ;
Weckhuysen, BM ;
Van Der Voort, P ;
Vansant, E ;
Schoonheydt, RA .
JOURNAL OF PHYSICAL CHEMISTRY B, 1998, 102 (41) :8005-8012
[8]   The hydrothermal synthesis of zeolites: Precursors, intermediates and reaction mechanism [J].
Cundy, CS ;
Cox, PA .
MICROPOROUS AND MESOPOROUS MATERIALS, 2005, 82 (1-2) :1-78
[9]   ZEOLITE AND MOLECULAR-SIEVE SYNTHESIS [J].
DAVIS, ME ;
LOBO, RF .
CHEMISTRY OF MATERIALS, 1992, 4 (04) :756-768
[10]   ANALYSIS OF ZEOLITE CRYSTALLIZATIONS USING THE CRYSTALLIZATION CURVE [J].
DENOUDEN, CJJ ;
THOMPSON, RW .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 1992, 31 (01) :369-373